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Sample records for khaki-ye kamyab ree

  1. REE from EOF

    NASA Astrophysics Data System (ADS)

    Jung, Eylee; Park, DaeKil

    2015-02-01

    It is well known that entanglement of formation (EOF) and relative entropy of entanglement (REE) are exactly identical for all two-qubit pure states even though their definitions are completely different. We think this fact implies that there is a veiled connection between EOF and REE. In this context, we suggest a procedure, which enables us to compute REE from EOF without relying on the converse procedure. It is shown that the procedure yields correct REE for many symmetric mixed states such as Bell-diagonal, generalized Vedral-Plenino, and generalized Horodecki states. It also gives a correct REE for less symmetric Vedral-Plenio-type state. However, it is shown that the procedure does not provide correct REE for arbitrary mixed states.

  2. Dr. Eberhard Rees

    NASA Technical Reports Server (NTRS)

    1970-01-01

    Dr. Eberhard Rees served as director of the Marshall Space Flight Center from March 1, 1970 until January 19, 1973 when he retired from NASA. Prior to his appointment as Director, Rees served as the Center's deputy director under Dr. Wernher von Braun, 1960-1970. Rees came to the United States as part of the Dr. Wernher von Braun's German Rocket team following World War II. He transferred to Huntsville, Alabama from Fort Bliss, Texas in 1950 to work for the Army's rocket program at Redstone Arsenal. From 1956 to 1960 he served as deputy director of development operations at the Army Ballistic Missile Agency under von Braun. In 1960 Rees was transferred to NASA's Marshall Center.

  3. Mantle metasomatism: the REE story.

    USGS Publications Warehouse

    Wilshire, H.G.

    1984-01-01

    Refractory rocks with light REE/heavy REE ratios > chondrites are common as xenoliths in basalts and kimberlites and are found in some oceanic peridotite massifs. Structural and major-element geochemical evidence from these rocks suggest that the metasomatic effects resulting in addition of light REE are local and are related to emplacement of partial melts. The melts are represented by dykes of pyroxenites, hydrous minerals and gabbro that were emplaced in mantle peridotites of various origins. Metasomatic interaction between dykes and peridotite wall rock results in light REE enrichment in peridotite and depletion in dykes relative to the original liquid. Differentiation of the intrusions and separation of residual liquids may further enhance the REE exchange and extend the volume of metasomatized peridotite. Differences in the relative abundances of altered peridotite in xenoliths and massifs are seen as a sampling problem rather than a difference in process.-L.diH.

  4. Gender- and Age-Specific REE and REE/FFM Distributions in Healthy Chinese Adults.

    PubMed

    Cheng, Yu; Yang, Xue; Na, Li-Xin; Li, Ying; Sun, Chang-Hao

    2016-01-01

    Basic data on the resting energy expenditure (REE) of healthy populations are currently rare, especially for developing countries. The aims of the present study were to describe gender- and age-specific REE distributions and to evaluate the relationships among glycolipid metabolism, eating behaviors, and REE in healthy Chinese adults. This cross-sectional survey included 540 subjects (343 women and 197 men, 20-79 years old). REE was measured by indirect calorimetry and expressed as kcal/day/kg total body weight. The data were presented as the means and percentiles for REE and the REE to fat-free mass (FFM) ratio; differences were described by gender and age. Partial correlation analysis was used to analyze the correlations between REE, tertiles of REE/FFM, and glycolipid metabolism and eating behaviors. In this study, we confirmed a decline in REE with age in women (p = 0.000) and men (p = 0.000), and we found that men have a higher REE (p = 0.000) and lower REE/FFM (p = 0.021) than women. Furthermore, we observed no associations among glycolipid metabolism, eating behaviors, and REE in healthy Chinese adults. In conclusion, the results presented here may be useful to clinicians and nutritionists for comparing healthy and ill subjects and identifying changes in REE that are related to aging, malnutrition, and chronic diseases. PMID:27598192

  5. REE Partitioning in Lunar Minerals

    NASA Technical Reports Server (NTRS)

    Rapp, J. F.; Lapen, T. J.; Draper, D. S.

    2015-01-01

    Rare earth elements (REE) are an extremely useful tool in modeling lunar magmatic processes. Here we present the first experimentally derived plagioclase/melt partition coefficients in lunar compositions covering the entire suite of REE. Positive europium anomalies are ubiquitous in the plagioclase-rich rocks of the lunar highlands, and complementary negative Eu anomalies are found in most lunar basalts. These features are taken as evidence of a large-scale differentiation event, with crystallization of a global-scale lunar magma ocean (LMO) resulting in a plagioclase flotation crust and a mafic lunar interior from which mare basalts were subsequently derived. However, the extent of the Eu anomaly in lunar rocks is variable. Fagan and Neal [1] reported highly anorthitic plagioclase grains in lunar impact melt rock 60635,19 that displayed negative Eu anomalies as well as the more usual positive anomalies. Indeed some grains in the sample are reported to display both positive and negative anomalies. Judging from cathodoluminescence images, these anomalies do not appear to be associated with crystal overgrowths or zones.

  6. Lough Ree Power Station, Lanesboro, Ireland

    SciTech Connect

    Wicker, K.

    2005-08-01

    The peat-fueled, 100-MW Lough Ree power station in the midlands of Ireland marks the beginning of a new era of electricity generation by the Electricity Supply Board. 30% more efficient than the old peat-fired power plant it replaced, Lough Ree uses a circulating fluidized bed boiler from Foster Wheeler to meet very strict air-emissions standards while exploiting an indigenous energy source. 3 figs., 2 tabs.

  7. REE/Fe variations in hydrothermal sediments: Implications for the REE content of seawater

    SciTech Connect

    Olivarez, A.M.; Owen, R.M. )

    1989-03-01

    Seafloor hydrothermal vent solutions exhibit rare earth element (REE) enrichments ranging between one to three orders of magnitude greater than average seawater. To assess the impact of these hydrothermal inputs on ocean chemistry, the authors have examined he behavior of REEs for hydrothermal sediments collected adjacent to two Pacific spreading ridge sites: the East Pacific Rise at 19{degree}S, and the Southern Juan de Fuca Ridge at 45{degree}N. In general, the REE/Fe ratios for both proximal and distal hydrothermal sediments are greater than vent solutions by a factor of 2 to 500, and these ratios increase with increasing distance away from the ridge axis. An evaluation of these results in the context of previous models of REE behavior indicates that, in fact, seawater experiences a net depletion in REEs as a result of hydrothermal activity. This is due primarily to the large scavenging capacity of iron oxyhydroxides which precipitate from these solutions. Such an interpretation explains why the REE content of seawater collected in the vicinity of hydrothermal vents is anomalously lower than normal seawater sampled from a comparable depth.

  8. REE in the Great Whale River estuary, northwest Quebec

    NASA Technical Reports Server (NTRS)

    Goldstein, Steven J.; Jacobsen, Stein B.

    1988-01-01

    A report on REE concentrations within the estuary of the Great Whale River in northwest Quebec and in Hudson Bay is given, showing concentrations which are less than those predicted by conservative mixing of seawater and river water, indicating removal of REE from solution. REE removal is rapid, occurring primarily at salinities less than 2 percent and ranges from about 70 percent for light REE to no more than 40 percent for heavy REE. At low salinity, Fe removal is essentially complete. The shape of Fe and REE vs. salinity profiles is not consistent with a simple model of destabilization and coagulation of Fe and REE-bearing colloidal material. A linear relationship between the activity of free ion REE(3+) and pH is consistent with a simple ion-exchange model for REE removal. Surface and subsurface samples of Hudson Bay seawater show high REE and La/Yb concentrations relative to average seawater, with the subsurface sample having a Nd concentration of 100 pmol/kg and an epsilon(Nd) of -29.3; characteristics consistent with river inputs of Hudson Bay. This indicates that rivers draining the Canadian Shield are a major source of nonradiogenic Nd and REE to the Atlantic Ocean.

  9. REE patterns of eucrites and their genetic implications

    NASA Astrophysics Data System (ADS)

    Shimizu, Hiroshi; Masuda, Akimasa

    1986-11-01

    Rare earth element (REE) abundances in eucrites were precisely determined on Juvinas, Pasamonte, Cachari, Stannern 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 Stannern 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.

  10. Multiple stages of hydrothermal REE remobilization recorded in fluorapatite in the Paleoproterozoic Yinachang Fe-Cu-(REE) deposit, Southwest China

    NASA Astrophysics Data System (ADS)

    Li, Xiaochun; Zhou, Mei-Fu

    2015-10-01

    The Yinachang deposit in the Kangdian region, Southwest China, contains large amounts of Fe, Cu and REE, and formed at ˜1700 Ma. In this deposit, there are three stages of alteration and mineralization, including pre-ore Na-(Fe) alteration, Fe-(REE) mineralization, and Cu-(REE) mineralization. In the Fe-(REE) mineralization stage, REE-rich fluorapatite, with total REE concentrations ranging from 10,700 to 34,000 ppm, formed together with magnetite. In the following Cu-(REE) mineralization stage, large amounts of REE, especially LREE, were leached out of the REE-rich fluorapatite due to the interaction between fluorapatite and Cl-, F-, CO2-, and Ca-rich, but REE-unsaturated fluids. The leaching of REE was associated with the removal of Si, Na, Th, U, Pb, and Ba, and modification of the oxygen isotope signature in the fluorapatite. During a ˜840 Ma tectonothermal event, REE-rich fluorapatite underwent the second interaction with oxidized, F-, CO2-, and possibly Cl-rich, but Na- and Ca-deficient fluids. Due to fluid-fluorapatite interaction, REE were removed from the fluorapatite, but were immediately reincorporated into new phases within the fluorapatite. Thus, the altered fluorapatite contains abundant REE mineral inclusions, including bastnäsite-(Ce), monazite-(Ce), and minor xenotime-(Y). A very small portion of the LREE were transported out of the fluorapatite, and formed bastnäsite-(Ce) and monazite-(Ce) grains in the vicinity of the altered fluorapatite. In addition to the metasomatism of fluorapatite, allanite and "primary" synchysite-(Ce) from the Cu-(REE) mineralization stage were also altered with variable replacement of allanite by an assemblage of synchysite-(Ce) + chlorite ± bastnäsite-(Ce) and "primary" synchysite-(Ce) by bastnäsite-(Ce). These styles of alteration were possibly synchronous with the second alteration phase of the fluorapatite. This study demonstrates that REE can be mobilized during multiple stages of hydrothermal activities and

  11. Genesis of ion-adsorption type REE ores in Thailand

    NASA Astrophysics Data System (ADS)

    Sanematsu, K.; Yoshiaki, K.; Watanabe, Y.

    2012-04-01

    Ion-adsorption type REE deposits, which have been economically mined only in southern China, are predominant supply sources for HREE in the world. The ore bodies consist of weathered granites called ion-adsorption ores. The majority of REE (>50 %) are electrostatically adsorbed onto weathering products in the ores and they can be extracted by ion exchange using an electrolyte solution (e.g., ammonium sulfate solution). Recently the occurrences of ion-adsorption ores have been reported in Indochina, SE Asia. In this study, we discuss geochemical and mineralogical characteristics of parent granites and weathered granites in Thailand in order to reveal the genesis of ion-adsorption ores. Permo-Triassic and Cretaceous-Paleogene granite plutons are distributed from northern Thailand to western Indonesia through eastern Myanmar and Peninsular Malaysia. They are mostly ilmenite-series calcalkaline biotite or hornblende-biotite granites. REE contents of the granites range from 60 to 600 ppm and they are relatively high in Peninsula Thailand. REE-bearing minerals consist mainly of apatite, zircon, allanite, titanite, monazite and xenotime. Some I-type granites contain REE fluorocarbonate (probably synchysite-(Ce)) in cavities and cracks in feldspars and it is the dominant source of REE for ion-adsorption ores because the fluorocarbonate is easily soluble during weathering. In contrast, insoluble monazite and xenotime are not preferable for ion-adsorption ores although they are common ore minerals of placer REE deposits. Weathered granites show REE contents ranging from 60 to 1100 ppm in Thailand because REE are relatively immobile compared with mobile elements (e.g., Na, K, Ca). In the weathered granites, REE are contained in residual minerals and secondary minerals and are adsorbed onto the surface of weathering products. A weathering profile of granite with ion-adsorption type mineralization can be divided into upper and lower parts based on REE enrichment and Ce

  12. Anomalous REE patterns in unequilibrated enstatite chondrites: Evidence and implications

    NASA Technical Reports Server (NTRS)

    Crozaz, Ghislaine; Hsu, Weibiao

    1993-01-01

    We present here a study of Rare Earth Element (REE) microdistributions in unequilibrated enstatite chondrites (EOC's). Although the whole rock REE contents are similar in both unequilibrated and equilibrated chondrites, the host minerals of these refractory elements are different. In the least equilibrated ordinary chondrites (UOC's), the REE reside mainly in glass whereas, in their more equilibrated counterparts, the bulk of the REE is in calcium phosphate, a metamorphic mineral that formed by oxidation of phosphorous originally contained in metal. In the smaller group of enstatite (E) chondrites, calcium phosphate is absent and the phase that contains the highest REE concentrations is a minor mineral, CaS (oldhamite), which contains approximately 50 percent of the total Ca present. In E chondrites, elements typically considered to be lithophiles (such as Ca and Mn) occur in sulfides rather than silicates. This indicates formation under extremely reducing conditions, thus in a region of the solar nebula distinct from those that supplied the more abundant ordinary and carbonaceous chondrites. Previously, we observed a variety of REE patterns in the oldhamite of UEC's; they range from almost flat to some with pronounced positive Eu and Yb anomalies. Here, we searched for complementary REE patterns in other minerals from E chondrites and found them in the major mineral, enstatite. Whenever Eu and Yb anomalies are present in this mineral, they are always negative.

  13. REE-bearing minerals in the Rapakavi Grante, Southern Finland

    NASA Astrophysics Data System (ADS)

    Al-Ani, Thair

    2015-11-01

    The studied rock samples belong to the classic 1615-1645 Ma Wiborg Rapakivi granite terrane of southeastern Finland. Geochemical studies show that the rapakivi granites and associated rocks form metaluminous to peraluminous A-type granites and plot in the "within plate granites (WPG)" field on the tectonic discriminate diagrams from the Onkamaa, Suomenniemi and Luumäki. The rapakivi granite displays enrichment of light over heavy REE (LREE/HREE = 2-34) and usually negative Eu anomalies (Eu/Eu* = 0.01 - 1.4). Enrichment in REE in some studied samples is confined to highly fractionated portions of the Rapakivi granite. Fractional crystallization of the evolving fluorite-rich peraluminous granitic magma was accompanied, particularly at later stages by fluid fractionation, which plays an important role in the genesis of the REE-mineralization. The studied rapakivi granites host REE-minerals including monazite-(Ce), allanite (Ce), bastnäsite (Ce), xenotime, thorite and REE-bearing mineral apatite. Monazite and allanite are the most important REE carriers in the studied granites and these minerals are strongly enriched in the LREE.Monazites are hosted in apatite, quartz, plagioclase, K-feldspar, and biotite. Grain size of monazite is variable ranging from 50 to >100 μm.Monazite contains 48-68 wt% REE2O3, 24.3-29.3 wt% P2O5 and low Th<1.5 wt%ThO2. The Y, REE, U, Th-bearing minerals are not commonly associated with the primary minerals except for Th-bearing minerals, which occur as silicates (e.g. thorite, ThSiO4); and/or replace other elements in the structure of some accessory mineral, especially xenotime, brabantite, zircon, and apatite. Electron probe microanalysis (EPMA) provides an indication of solid solution series between thorite-xenotimezircon, which are related to hydrothermal solutions enriched in REE, Y, P, U, F, and Zr.

  14. Battery related cobalt and REE flows in WEEE treatment.

    PubMed

    Sommer, P; Rotter, V S; Ueberschaar, M

    2015-11-01

    In batteries associated with waste electrical and electronic equipment (WEEE), battery systems can be found with a higher content of valuable and critical raw materials like cobalt and rare earth elements (REE) relative to the general mix of portable batteries. Based on a material flow model, this study estimates the flows of REE and cobalt associated to WEEE and the fate of these metals in the end-of-life systems. In 2011, approximately 40 Mg REE and 325 Mg cobalt were disposed of with WEEE-batteries. The end-of-life recycling rate for cobalt was 14%, for REE 0%. The volume of waste batteries can be expected to grow, but variation in the battery composition makes it difficult to forecast the future secondary raw material potential. Nevertheless, product specific treatment strategies ought to be implemented throughout the stages of the value chain. PMID:26054962

  15. Multi-collector SIMS analysis of REE in zircon

    NASA Astrophysics Data System (ADS)

    Whitehouse, M.

    2003-04-01

    Several recent studies have highlighted the utility of rare earth element (REE) analysis of zircon in facilitating a link between U-Pb geochronology and petrogenesis. Such analyses face a number of analytical challenges, notably very low concentration levels of trivalent light REE's (La-Sm) and, for SIMS, interferences from matrix (ZrSiO species on La, Ce and Pr) and light REE oxides on heavy REE. Low mass-resolution SIMS instruments generally use large energy offsets and/or peak deconvolution methods to overcome these problems. Lack of a well-characterised zircon standard means that analyses are generally normalised to synthetic glass standards with energy offsets used to minimise matrix effects. This study reports the application of a multicollector equipped Cameca IMS1270 to analysis of REE in zircon. The IMS1270 multicollector consists of five moveable trolleys which, in the configuration fitted in Stockholm, are each equipped with narrow ion counting electron multipliers (EM's). An extreme dispersion limit from 7.8% to +7.8% relative to axial mass is permitted by the moveable trolleys. At closest approach (ca. 0.48%) simultaneous Pb isotope measurement is possible. A three position exit slit facilitates common nominal mass resolutions between 2400 and 8000. The fixed axial collector with its continuously variable exit slit may be used together with the trolley mounted EM's permitting simultaneous measurement in six detectors. In this latter configuration, used here for REE measurements, the dispersion range from 1.6% to +5.1% is unavailable for the trolleys. The collector configuration used for zircon REE analysis puts the six lightest REE (La, Ce, Pr, Nd, Sm, Eu) simultaneously into the five moveable EM's at MRP ca. 3800, adequately resolving ZrSiO interferences, and the fixed axial EM at MRP ca. 1500, the latter measuring 144Nd which is unaffected by molecular interferences. A sample high voltage offset of -45V relative to the centred energy peak (30e

  16. REE in karst bauxites: the Campania example (southern Italy)

    NASA Astrophysics Data System (ADS)

    Mondillo, N.; Boni, M.; Balassone, G.; Rollinson, G.

    2012-04-01

    Global production of Rare Earth Element (REE) has dramatically increased in the last years, hence the strong interest to identify new deposits and to understand the processes responsible for their formation. Among REE concentrations related to weathering, the current targets are represented by the ion-adsorption deposit-types, occurring in China, in which REEs are adsorbed onto the surface of clays. Laterites have been also intensively investigated since the discovery of the secondary deposit of Mount Weld (Australia). Most REEs behave as immobile elements in laterites, and tend to be enriched compared to the underlying parent rocks. Many authors debate on a possible REE fractionation along the laterite profiles, resulting in the formation of supergene LREE-minerals. Bauxites are economic Al accumulations, derived from the weathering of alumosilicate-rich parent rocks resulting in the development of laterite profiles. Components as Ca, Mg, K, Si are leached and residual Fe, Al and Ti precipitate in form of hematite>>goethite, gibbsite [Al(OH)3] or amorphous Al hydroxides and anatase. Metabauxites can contain boehmite or diaspore [AlO(OH)]. Chemical composition (including REEs content) of lateritic bauxites generally mirrors the original composition of the parent rock. Geochemistry of REEs in karst bauxites, which lay on carbonate bedrocks and may be also allochthonous to them, is not so straightforward. Cretaceous karst bauxite deposits in the Apennine chain (Southern Italy) are presently uneconomic. A full mineralogical and geochemical study has been performed on several deposits of the Campania district, and three representative profiles have been sampled. In all deposits the bauxite ore has an oolitic-pisolitic texture, but contains also detrital intervals. The mineral association consists of boehmite, kaolinite and hematite, with less goethite and anatase. The main REE-bearing mineral is detrital monazite. In detail, we could detect (SEM) other LREE

  17. Isomorphism of actinides and REE in synthetic ferrite garnets

    NASA Astrophysics Data System (ADS)

    Livshits, T. S.

    2010-02-01

    The reprocessing of spent nuclear fuel (SNF) is accompanied by the formation of liquid high-level radioactive waste (HLW). To increase the safety of handling HLW, it is proposed to extract actinide isotopes (An) and REE from them. These elements may be incorporated into crystalline matrices, e.g., based on ferrites with garnet structure, and then disposed in a geologic repository. The actinide-REE fraction is characterized by a complex composition. In addition to major components (An and REE), Al, Si, Na, and Sn occur therein in small amounts (a few wt %). Possible incorporation of the admixtures into ferrite garnets, as well as their effect on the phase composition of matrices and Th, Ce, Gd, and La contents were studied. It was shown that admixtures enter into garnet by means of isomorphic replacement. The properties of samples change only when admixtures are added in amounts exceeding their concentrations in HLW. The ability of ferrite garnets to accumulate significant amounts of An, REE, and admixture elements makes them suitable for use as matrices in immobilizing actinide-REE HLW of complex composition.

  18. REE and Strontium Partition Coefficients for Nakhla Pyroxenes

    NASA Technical Reports Server (NTRS)

    Oe, K.; McKay, G.; Le, L.

    2001-01-01

    We present new partition coefficients for REE and Sr determined using a synthetic melt that crystallizes pyroxenes very similar in composition to Nakhla pyroxene cores. We believe these are the most appropriate partition coefficients to use in studying Nakhla Additional information is contained in the original extended abstract..

  19. Vapour transport of rare earth elements (REE) in volcanic gas: Evidence from encrustations at Oldoinyo Lengai

    NASA Astrophysics Data System (ADS)

    Gilbert, C. D.; Williams-Jones, A. E.

    2008-10-01

    Fumarolic encrustations and natrocarbonatite lava from the active crater of Oldoinyo Lengai volcano, Tanzania, were sampled and analysed. Two types of encrustation were distinguished on the basis of their REE content, enriched (~ 2800-5600 × [REE chondrite]) and depleted (~ 100-200 × [REE chondrite]) relative to natrocarbonatite (1700-1900 × [REE chondrite]. REE-enriched encrustations line the walls of actively degassing fumaroles, whereas REE-depleted encrustations occur mainly along cracks in and as crusts on cooling natrocarbonatite lava flows; one of the low REE encrustation samples was a stalactite from the wall of a possible fumarole. The encrustations are interpreted to have different origins, the former precipitating from volcanic gas and the latter from meteoric/ground water converted to steam by the heat of the overlying lava flow(s). REE-profiles of encrustations and natrocarbonatite are parallel, suggesting that there was no preferential mobilization of specific REE by either volcanic vapour or meteoric water vapour. The elevated REE-content of the first group of encrustations suggests that direct REE-transport from natrocarbonatite to volcanic vapour is possible. The REE trends observed in samples precipitating directly from the volcanic vapour cannot be explained by dry volatility based on the available data as there is no evidence in the encrustation compositions of the greatly enhanced volatility predicted for Yb and Eu. The observed extreme REE-fractionation with steep La/Sm slopes parallel to those of the natrocarbonatite reflects solvation and complexation reactions in the vapour phase that did not discriminate amongst the different REE or similar transport of REE in both the natrocarbonatite magma and its exsolving vapour. The low concentrations of REE in the encrustations produced by meteoric vapour suggest that the temperature was too low or that this vapour did not contain the ligands necessary to permit significant mobilization of the REE.

  20. Systematic Investigation of REE Mobility and Fractionation During Continental Shale Weathering Along a Climate Gradient

    NASA Astrophysics Data System (ADS)

    Jin, L.; Ma, L.; Dere, A. L. D.; White, T.; Brantley, S. L.

    2014-12-01

    Rare earth elements (REE) have been identified as strategic natural resources and their demand in the United States is increasing rapidly. REE are relatively abundant in the Earth's crust, but REE deposits with minable concentrations are uncommon. One recent study has pointed to the deep-sea REE-rich muds in the Pacific Ocean as a new potential resource, related to adsorption and concentration of REE from seawater by hydrothermal iron-oxyhydroxides and phillipsite (Kato et al., 2010). Finding new REE deposits will be facilitated by understanding global REE cycles: during the transformation of bedrock into soils, REEs are leached into natural waters and transported to oceans. At present, the mechanisms and factors controlling release, transport, and deposition of REE - the sources and sinks - at Earth's surface remain unclear. Here, we systematically studied soil profiles and bedrock in seven watersheds developed on shale bedrock along a climate transect in the eastern USA, Puerto Rico and Wales to constrain the mobility and fractionation of REE during chemical weathering processes. In addition, one site on black shale (Marcellus) bedrock was included to compare behaviors of REEs in organic-rich vs. organic-poor shale end members under the same environmental conditions. Our investigation focused on: 1) the concentration of REEs in gray and black shales and the release rates of REE during shale weathering, 2) the biogeochemical and hydrological conditions (such as redox, dissolved organic carbon, and pH) that dictate the mobility and fractionation of REEs in surface and subsurface environments, and 3) the retention of dissolved REEs on soils, especially onto secondary Fe/Al oxyhydroxides and phosphate mineral phases. This systematic study sheds light on the geochemical behaviors and environmental pathways of REEs during shale weathering along a climosequence.

  1. The first data on the vertical REE distribution in taiga soils of the Russian Far East

    NASA Astrophysics Data System (ADS)

    Bryanin, S. V.; Sorokina, O. A.

    2015-10-01

    Coarse humic brown soils formed on different rocks under natural conditions of southern taiga of the Upper Priamur'e were studied. Concentration and distribution of REE in organic-mineral and metamorphic soil horizons were estimated. Soils inherit REE distribution in underlying rocks sitll at lower concentrations. The maximal REE concentrations are found in metamorphic soil horizon and the lowest ones in humic-accumulative. Soil formation processes have an effect on REE concentration in soils, but do not change their distribution.

  2. Rees algebras, Monomial Subrings and Linear Optimization Problems

    NASA Astrophysics Data System (ADS)

    Dupont, Luis A.

    2010-06-01

    In this thesis we are interested in studying algebraic properties of monomial algebras, that can be linked to combinatorial structures, such as graphs and clutters, and to optimization problems. A goal here is to establish bridges between commutative algebra, combinatorics and optimization. We study the normality and the Gorenstein property-as well as the canonical module and the a-invariant-of Rees algebras and subrings arising from linear optimization problems. In particular, we study algebraic properties of edge ideals and algebras associated to uniform clutters with the max-flow min-cut property or the packing property. We also study algebraic properties of symbolic Rees algebras of edge ideals of graphs, edge ideals of clique clutters of comparability graphs, and Stanley-Reisner rings.

  3. Fractionation mechanisms of rare earth elements (REEs) in hydroponic wheat: an application for metal accumulation by plants.

    PubMed

    Ding, Shiming; Liang, Tao; Zhang, Chaosheng; Huang, Zechun; Xie, Yaning; Chen, Tongbin

    2006-04-15

    Fractionations of rare earth elements (REEs) in wheat (Triticum aestivum L.) were observed through application of exogenous mixed REEs under hydroponic conditions. Middle REE (MREE), light REE (LREE), and heavy REE (HREE) enrichments were found in roots, stems, and leaves, respectively, accompanied by the tetrad effect (an effect that can cause a split of REE patterns into four consecutive segments) in these organs. Investigations into REE speciation in roots and in the xylem sap with X-ray absorption spectroscopy (XAS) and nanometer-sized TiO2 adsorption techniques, associated with other controlled experiments, demonstrated that REE fractionations in wheat were caused by the combined effects of chemical precipitation, cell wall absorption, and solution complexation by organic ligands in the xylem vessels. REE fractionations in wheat, which were derived from the small differences of chemical properties across REE series, may reflect a sensitive internal chemical environment that influences plant accumulation for REEs and their analogues actinide radionuclides. PMID:16683609

  4. REE incorporation and behaviour in aquatic turtles as a consequence of environmental exposure and biological processes

    NASA Astrophysics Data System (ADS)

    Censi, P.; Randazzo, L. A.; D'Angelo, S.; Cuttitta, A.; Saiano, F.

    2012-04-01

    Rare Earth Elements (REE) contents in Emys trinacris have been investigated for the first time in order to recognise effects of the chemistry of the environment on the composition of biological fluids. Representing radionuclides a potential health risk for living organisms in case of incorporation in tissues and being REE geochemical analogues of actinides in hydrosphere, this study was focused on investigation of REE behaviour in whole blood and esoskeleton of selected individuals of Emys trinacris. The choice of this species is related to its amphibian character that allowed us to evidence environmental stress in terms of composition of environmental freshwaters whose REE compositions were investigated and compared with blood samples. Moreover effects induced by different environmental conditions were investigated collecting samples in two sites characterised by absence of an anthropogenic signature (GT site) and subjected to strong anthropogenic pressure in terms of wastewater input (SIC site), respectively. In both sites REE contents in whole blood samples of studied turtles are quite similar even if in GT site the highest REE contents have been recognised. Shale-normalised REE patterns show very similar REE behaviour with light REE (LREE) enrichments with respect to heavier REE (HREE), mainly in samples from anthropized site. If REE concentrations in whole blood are normalised to the composition of environmental waters, calculated REE patterns show upward concave shapes centred on Gd that are more pronounced in samples from GT site because their patterns are more enriched in LREE. The last features observed in blood samples from GT can be related to larger REE contents occurred in environmental water from this site with respect to waters collected in SIC site, suggesting that a relationship occurs between REE contents in environmental and biological fluids. Since MREE depletions were observed in waters experiencing phosphate crystallization, observed REE

  5. Expanding the REE Partitioning Database for Lunar Materials

    NASA Technical Reports Server (NTRS)

    Rapp, Jennifer F.; Draper, David S.

    2014-01-01

    Positive europium anomalies are ubiquitous in the plagioclase-rich rocks of the lunar highlands, and complementary negative Eu anomalies are found in most lunar basalts. This is taken as evidence of a large-scale differentation event, with crystallization of a global-scale lunar magma ocean (LMO) resulting in a plagioclase flotation crust and a mafic lunar interior from which mare basalts were later derived. However, the extent of the Eu anomaly in lunar rocks is variable. Some plagioclase grains in a lunar impact rock (60635) have been reported to display a negative Eu anomaly, or in some cases single grains display both positive and neagtive anomalies. Cathodoluminescence images reveal that some crystals have a negative anomaly in the core and positive at the rim, or vice versa, and the negative anomalies are not associated with crystal overgrowths. Oxygen fugacity is known to affect Eu partitioning into plagioclase, as under low fO2 conditions Eu can be divalent, and has an ionic radius similar to Ca2+ - significant in lunar samples where plagioclase compositions are predominantly anorthitic. However, there are very few experimental studies of rare earth element (REE) partitioning in plagioclase relevant to lunar magmatism, with only two plagioclase DEu measurements from experiments using lunar materials, and little data in low fO2 conditions relevant to the Moon. We report on REE partitioning experiments on lunar compositions. We investigate two lunar basaltic compositions, high-alumina basalt 14072 and impact melt breccia 60635. These samples span a large range of lunar surface bulk compositions. The experiments are carried out at variable fO2 in 1 bar gas mixing furnaces, and REE are analysed by and LA-ICP-MS. Our results not only greatly expand the existing plagioclase DREE database for lunar compositions, but also investigate the significance of fO2 in Eu partitioning, and in the interpretation of Eu anomalies in lunar materials.

  6. EXAFS study on the cause of enrichment of heavy REEs on bacterial cell surfaces

    NASA Astrophysics Data System (ADS)

    Takahashi, Yoshio; Yamamoto, Mika; Yamamoto, Yuhei; Tanaka, Kazuya

    2010-10-01

    Rare earth element (REE) pattern is a unique geochemical tracer and has been measured for various natural materials. Among these, the REE distribution pattern between bacteria and water exhibits anomalous enrichment in the heavy REE (HREE) part, which can act as a signature of bacteria-related materials in natural samples. In this study, the REE binding site on the cell surface of a Gram-positive bacterium ( Bacillus subtilis) responsible for HREE enrichment has been identified using extended X-ray absorption fine structure (EXAFS) coupled with a study of the variation in REE distribution patterns. The EXAFS data showed that the HREEs form complexes with multiple phosphate site (including phosphoester site) with a larger coordination number (CN) at lower REE-bacteria ratios ([REE]/[bac]), while light and middle REEs form complexes to the phosphate site with a lower CN. The fraction coordinated to carboxylate increased for all REEs with increasing [REE]/[bac] ratio. On the other hand, the enrichment of HREE in the REE distribution patterns of the bacteria was less marked with increasing [REE]/[bac] ratio. This result is consistent with the EXAFS data, because the REE pattern of surface complex with multiple phosphate in a reference material exhibits a monotonous increase for heavier REE, while phosphate surface complex with a low CN and a carboxylate site reach a maximum around Sm and Eu. Based on these results, it is clear that the REE are primarily bound to the phosphate site and subsequently to the carboxylate site on the bacterial cell surface. Regarding the pH dependence in the range (3 < pH < 7), both the EXAFS and REE pattern data indicate that the fraction of REE-carboxylate increased as the pH increases. The results above obtained for B. subtilis were also valid for Escherichia coli, a Gram-negative bacterium, showing that similar phosphate and carboxylate sites are also available in the cell walls of E. coli, or other Gram negative bacteria. In all our

  7. REE mobility during the alteration of Carbonatite and their economic potential.

    NASA Astrophysics Data System (ADS)

    Marien, Christian; Dijkstra, Arjan; Wilkins, Colin

    2016-04-01

    The supply risk of Rare Earth Elements is an unpredictable economic factor for the future application and development of modern technology for the EU. Therefore a better understanding of REE mobilisation during hydrothermal alteration of Carbonatites is essential for a safer supply of REE in general. The hydrothermal alteration of Carbonatite within the Fen Complex (Norway) forms a fine grained red hematized rock type, called Rødbergite, which is partially enriched in REE. The variation of REE within the Rødbergite is poorly understood and problematic for any future REE exploitation from Rødbergite. A genetic model of the formation of Rødbergite will provide more information about the economic potential of Rødbergite. The gradual transformation of carbonatite to Rødbergite is not easily observable due to sparse outcrop in the Fen Complex. A fresh road cut near the Bjørndallen farm (Fen Complex) provides a unique insight to the progressive hydrothermal alteration from carbonatite to Rødbergite and is therefore crucial for a genetic model of the formation of Rødbergite. 14 Samples were taken along the profile. The mineralogical, geochemical and textural characterization of the samples using the SEM as well as major-, trace- and isotopic elemental data revealed the breakdown of the primary minerals due to the infiltration of an oxidizing fluid along grain boundaries. The primary REE-minerals in unaltered Carbonatite are REE fluorocarbonates. With the increasing alteration to Rødbergite REE fluorocarbonates are progressively replaced by hematite. In contrast, monazite - a REE-phosphate - is the dominant REE mineral species in the Rødbergite. A transitional Rødbergite sample shows apatite aggregates with a strong preferential concentration of monazite along the rim of the apatite aggregates. This observation provides strong evidence for the solution of REE in the primary rock (carbonatite) by fluids and later precipitation of REE along phosphate bearing

  8. REE compositions in fossil vertebrate dental tissues indicate biomineral preservation

    NASA Astrophysics Data System (ADS)

    Žigaite, Ž.; Kear, B.; Pérez-Huerta, A.; Jeffries, T.; Blom, H.

    2012-04-01

    Rare earth element (REE) abundances have been measured in a number of Palaeozoic and Mesozoic dental tissues using Laser Ablation Inductively Coupled Plasma Mass-spectrometry (LA-ICP-MS). Fossil vertebrates analysed comprise scales and tesserae of Silurian and Devonian acanthodians, chondrichthyans, galeaspids, mongolepids, thelodonts, as well as teeth of Cretaceous lungfish and marine reptiles. The evaluation of fossil preservation level has been made by semi-quantitative spot geochemistry analyses on fine polished teeth and scale thin sections, using Energy Dispersive X-ray Spectroscopy (EDS). Fossil teeth and scales with significant structure and colour alteration have shown elevated heavy element concentrations, and the silicification of bioapatite has been common in their tissues. Stable oxygen isotope measurements (δ18O) of bulk biomineral have been conducted in parallel, and showed comparatively lower heavy oxygen values in the same fossil tissues with stronger visible alteration. Significant difference in REE concentrations has been observed between the dentine and enamel of Cretaceous plesiosaurs, suggesting the enamel to be more geochemically resistant to diagenetic overprint.

  9. Ion microprobe investigation of plagioclase and orthopyroxene from lunar Mg-suite norites: Implications for calculating parental melt REE concentrations and for assessing postcrystallization REE redistribution

    SciTech Connect

    Papike, J.J.; Fowler, G.W.; Shearer, C.K.; Layne, G.D.

    1996-10-01

    The lunar Mg-suite, which includes dunites, troctolites, and norites, makes up to 20-30% of the Moon`s crust down to a depth of {approximately}60 km. The remainder is largely anorthosite. This report focuses on norites (which consist mostly of orthopyroxene and plagioclase) because we have found that both phases are effective recorders of their parental melt compositions. In an earlier report, we analyzed orthopyroxene from twelve samples (three from Apollo 14, two from A-15, and seven from A-17) by orthopyroxene from twelve samples (three from Apollo 14, two from A-15, and seven from A-17) by SIMS for eight REE (La, Ce, Nd, Sm, Eu, Dy, Er, Yb). Inversion of these data to estimated melt compositions yielded extremely high REE concentrations similar to KREEP. In this study, we report SIMS REE data for plagioclase from these same twelve samples. The major objective of this study is to estimate parental REE concentrations from both orthopyroxene and plagioclase data to see if both data inversions produce concordant from both orthopyroxene and plagioclase data to see if both data inversions produce concordant melt compositions and thus better constrain the composition of melts parental to Mg-suite norites. The estimated REE concentrations from both phases show some evidence of slight postcrystallization REE redistribution. Comparison of the observed ratio of REE for pyroxene/plagioclase to the ratio of the Ds for pyroxene/plagioclase is consistent with REE redistribution which involves LREE diffusing from pyroxene into plagioclase and HREE diffusing from plagioclase into pyroxene. However, apparently these postcrystallization exchanges have not seriously affected our ability to estimate melt REE concentrations. 34 refs., 7 figs., 5 tabs.

  10. REE speciation in low-temperature acidic waters and the competitive effects of aluminum

    USGS Publications Warehouse

    Gimeno, Serrano M.J.; Auque, Sanz L.F.; Nordstrom, D.K.

    2000-01-01

    The effect of simultaneous competitive speciation of dissolved rare earth elements (REEs) in acidic waters (pH 3.3 to 5.2) has been evaluated by applying the PHREEQE code to the speciation of water analyses from Spain, Brazil, USA, and Canada. The main ions that might affect REE are Al3+, F-, SO42-, and PO43-. Fluoride, normally a significant complexer of REEs, is strongly associated with Al3+ in acid waters and consequently has little influence on REEs. The inclusion of aluminum concentrations in speciation calculations for acidic waters is essential for reliable speciation of REEs. Phosphate concentrations are too low (10-4 to 10-7 m) to affect REE speciation. Consequently, SO42- is the only important complexing ligand for REEs under these conditions. According to Millero [Millero, F.J., 1992. Stability constants for the formation of rare earth inorganic complexes as a function of ionic strength. Geochim. Cosmochim. Acta, 56, 3123-3132], the lanthanide sulfate stability constants are nearly constant with increasing atomic number so that no REE fractionation would be anticipated from aqueous complexation in acidic waters. Hence, REE enrichments or depletions must arise from mass transfer reactions. (C) 2000 Elsevier Science B.V. All rights reserved.

  11. Direct dating and characterization of the Pope's Hill REE Deposit, Labrador

    NASA Astrophysics Data System (ADS)

    Chafe, A. N.; Hanchar, J. M.; Fisher, C.; Piccoli, P. M.; Crowley, J. L.; Dimmell, P. M.

    2012-12-01

    The Pope's Hill rare earth element (REE) trend (PHT) is located approximately 100 km southwest of Happy Valley-Goose Bay, along the Trans Labrador Highway, in central Labrador. Whole-rock geochemical analyses of the main REE-bearing unit indicate total rare earth element contents ranging from 1 to 22 weight percent (wt%) REE3+. The REE-enriched unit is hosted within a hydrothermally altered syenite, trending northeast and traceable for approximately 2.8km. Samples of ore, host rock, and country rock, were collected from throughout the trend in order to: 1) quantify which phases concentrate the REE and their abundances and distribution in the ore; and 2) use in situ LA-ICPMS and ID-TIMS U-Pb geochronology and in situ Sm-Nd isotopes using LA-MC-ICPMS in monazite from the ore and host rock to constrain the timing of mineralization and determine the source of the REE. These data will help develop predictive models for this type of mineral deposit elsewhere. The PHT is defined as the host syenite and REE-enriched segregations; two contrasting lithologies. The rare earth element minerals (REE) occur in millimeter- to centimeter-scale pods that are locally discontinuous. The REE are hosted in a variety of silicate, phosphate, carbonate, and niobate phases; with a majority hosted in allanite(-Ce), titanite(-Ce), monazite(-Ce), britholite(-Ce); and a minor percentage in REE-carbonates and fergusonite(-Nd). Both apatite and titanite occur in two different compositional forms that range in chemistry from end-member stoichiometric apatite and titanite to highly REE-enriched - apatite-britholite and titanite(-Ce), where chemical substitutions, such as Si4+ + REE3+ substitute for Ca2+ + P5+ in apatite and REE3+ + Fe3+ substitute for Ca2+ + Ti4+ in titanite in order to incorporate up to ~40 wt% REE2O3 in both minerals. The U-Pb geochronology indicate that allanite, titanite(-Ce), monazite and fergusonite crystallized from ~1060 to ~940 Ma, a period spanning ~120 Ma. Sm-Nd tracer

  12. Partitioning in REE-saturating minerals - Theory, experiment, and modelling of whitlockite, apatite, and evolution of lunar residual magmas

    NASA Technical Reports Server (NTRS)

    Jolliff, Bradley L.; Haskin, Larry A.; Colson, Russell O.; Wadhwa, Meenakshi

    1993-01-01

    Compositions, including REEs determined by ion microprobe, of apatite and whitlockite in lunar rock assemblages rich in incompatible trace elements, are presented. Concentrations of REEs in lunar whitlockites are high, ranging from about 1.2 to 2.1 REEs (lanthanides + Y) per 56 oxygens. This slightly exceeds the level of two REE atoms per 56 oxygens at which the dominant substitution theoretically becomes saturated. This saturation effect leads to whitlockite REE(3+) D values at typical lunar whitlockite REE concentrations which are 30-40 percent lower than the D values at low concentrations. The halogen-to-phosphorous ratio in lunar melts is a key factor determining the REE distribution with crystalline assemblages. As long as P and REE concentrations of melts are in KREEP-like proportions, one or both of the phosphates will saturate in melts at similar REE concentrations.

  13. Crystallization process of zircon and fergusonite during hydrothermal alteration in Nechalacho REE deposit, Thor Lake, Canada

    NASA Astrophysics Data System (ADS)

    Hoshino, M.; Watanabe, Y.; Murakami, H.; Kon, Y.; Tsunematsu, M.

    2012-04-01

    The core samples of two drill holes, which penetrate sub-horizontal mineralized horizons at Nechalacho REE deposit in the Proterozoic Thor Lake syenite, Canada, were studied in order to clarify magmatic and hydrothermal processes that enriched HFSE (e.g. Zr, Nb, Y and REE). Zircon is the most common REE minerals in Nechalacho REE deposit. The zircon is divided into five types as follows: Type-1 zircon occurs as single grain in phlogopite and the chondrite-normalized REE pattern is characterized by a steeply-rising slope from the LREE to the HREE with a positive Ce-anomaly and negative Eu-anomaly. This chemical characteristic is similar to that of igneous zircon. Type-2 zircon consists of HREE-rich magmatic porous core and LREE-Nb-F-rich hydrothermal rim. This type zircon is mostly included in phlogopite and fluorite, and occasionally in microcline. Type-3 zircon is characterized by euhedral to anhedral crystal, occurring in a complex intergrowth with REE fluorocarbonates. Type-3 zircons have high contents of REE, Nb and fluorine. Type-4 zircon consists of porous-core and -rim zones, but their chemical compositions are similar to each other. This type zircon is a subhedral crystal rimmed by fergusonite. Type-5 zircon is characterized by smaller, porous and subhedral to anhedral crystals. The interstices between small zircons are filled by fergusonite. Type-4 and -5 zircons show low REE and Nb contents. Occurrences of these five types of zircon are different according to the depth and degree of the alteration by hydrothermal solutions rich in F- and CO3 of the two drill holes, which permit a model for evolution of the zircon crystallization in Nechalacho REE deposit as follows: (1) type-1 (single magmatic zircon) is formed in miaskitic syenite. (2) LREE-Nb-F-rich hydrothermal zircon formed around HREE-rich magmatic zircon (type-2 zircon); (3) type-3 zircon crystallized thorough F and CO3-rich hydrothermal alteration of type-2 zircon which formed the complex

  14. Diffusion of REE, Hf and Sr in Olivine

    NASA Astrophysics Data System (ADS)

    Remmert, P.; Dohmen, R.; Chakraborty, S.

    2008-12-01

    We have determined diffusion coefficients of the rare earth elements Ce, Nd, Sm, Eu, Lu, and also of Sr and Hf, in single crystals of natural olivine at atmospheric pressure, at an oxygen fugacity of 10-5 Pa and a temperature of 1275 °C. Sources of diffusants were thin films of olivine composition doped with the relevant elements. Thin films were produced by PLD (pulsed laser deposition) and RBS (Rutherford backscattering) was used to measure thickness and stoichiometry of the films as well as to analyze the concentration profiles. The concentration profiles were numerically fitted to yield the following diffusion coefficients (D, in m2/s): log DCe: -19.61 ± 0.21; log DNd: -19.54 ± 0.11; log DSm: -19.15 ± 0.05; log DEu: -19.10; log DLu: -19.00, log DHf: -20.23 ± 0.07; log DSr: -18.7. Diffusion coefficients of the rare-earth elements increase from Ce to Lu, demonstrating the role of ionic radius in controlling diffusion because all REE are trivalent. The tetravalent and divalent cations hafnium and strontium diffuse an order of magnitude slower and faster, respectively, than the REE in olivine. This highlights the important influence of ionic charge on diffusion rates. The diffusion coefficients of the REE are slower by a few orders of magnitudes than the diffusion rate of Cr in olivine [1]. The rates found in this study are slower than those assumed by a model [2] for compositional modification of melt inclusions in olivine. Use of our data in their calculations indicates that it will take longer to modify the composition of melt inclusions in olivine (millions of years rather than thousands of years) but the fractionation of HREE from LREE will be larger. [1] Ganguly J, Ito M (2006) Geochim Cosmochim Acta, 70, 799-809. [2] Cottrell E, Spiegelman M, Langmuir CH (2002) Geochem Geophys Geosyst, doi:10.1029/2001GC000205

  15. Comparing REE distribution in GEMAS agricultural soils and FOREGS topsoils-subsoils in Italy and Sweden

    NASA Astrophysics Data System (ADS)

    Petrosino, Paola; Sadeghi, Martiya; Andersson, Madelen; Albanese, Stefano; Dinelli, Enrico; Valera, Paolo; Ladenberger, Anna; Morris, George; Uhlbäck, Jo; Lima, Annamaria; De Vivo, Benedetto

    2014-05-01

    Scientific interest on Rare Earth Elements (REEs)-bearing media is increasing as a consequence of the rapidly growing demand of these important chemical resources, which are currently used in a large number of technical applications. In this study, Italian and Swedish REE data from the FOREGS database on topsoil and subsoils samples have been compared to the distribution of REEs in the GEMAS samples of agricultural soil (Ap), pertaining to regularly ploughed land to a depth of 20 cm. Principal Component Analysis (PCA) was carried out to identify patterns within both data sets. Investigation of the spatial distribution of REEs in FOREGS topsoil-subsoil and GEMAS Ap media for both countries revealed the prominent role of the geogenic component in the general REE geochemical pattern of the three solid media. Despite a similar REE content in the underlying parent material or bedrocks (alkaline igneous rocks, both intrusive and effusive in Italy, alkaline granites and pegmatites in Sweden), several distinct differences emerged between the two countries driven by climate, topography, age of the rock units and sediments, presence of mineralisations, type of soils and presence of glacial deposits. GEMAS agricultural soils form both countries show higher REEs contents than the corresponding subsoils and topsoils, which could be ascribed to the analytical method specifically set for REEs and the last generation ICP-MS instrument used by SGS Lab to analyze REEs in Ap soils. The REE content in Italian topsoil and subsoil is similar and there is a good agreement between the topsoils and Ap soils, which were collected from similar depth. Swedish subsoil is on the contrary more enriched in REEs with respect to topsoil, and Ap soils even display REE contents higher than subsoils. This anomalous REE concentrations in agricultural soil may originate from the fact that most of the arable land in Sweden has been located on glacial and postglacial deposits, rich in clay which has

  16. Influence of phosphate on mobility and adsorption of REEs during weathering of granites in Thailand

    NASA Astrophysics Data System (ADS)

    Sanematsu, Kenzo; Kon, Yoshiaki; Imai, Akira

    2015-11-01

    The Permo-Jurassic North Thai (NT) Granites and the Late Cretaceous to Paleogene Western Province (WP) Granites in Thailand are contrasting in terms of tectonic settings and chemical compositions. The NT Granites, which are dominated by S-type features, are characterized by lower SiO2 contents and higher P2O5 contents than the WP Granites in this study. In order to compare the mobility and adsorption of rare earth elements (REEs) during weathering of the two granite suites, geochemical analyses were conducted on the granite and weathered granites. The weathered WP Granites show wider ranges of REEs + Y (REY) contents, percentages of ion-exchangeable REY and Ce anomalies than the weathered NT Granites. These results indicate that REEs were less mobile during weathering of the NT Granites than those of the WP Granites. The low mobility of REEs can be explained by the occurrences of residual monazite and secondary REE phosphates which immobilize REEs during weathering. Therefore, in the weathered NT Granites, REEs are mostly contained in the phosphate minerals. In contrast, the weathered WP Granites are dominated by ion-exchangeable REEs (adsorbed REEs) which are likely to exist on the surface of clays. Previous studies and our study results suggest that the ion-exchangeable REEs in the weathered granites were probably sourced from weatherable allanite, titanite, apatite and/or REE fluorocarbonate, and rarely from monazite and zircon, which are resistant to weathering. The weathered granites of low phosphate contents potentially show high percentages of ion-exchangeable REY, although they can be influenced by the degree of hydrothermal alteration or weathering of granites.

  17. REE Sorption Study of Seived -50 +100 Mesh Fraction of Media #1 in Brine #1 at Different Concentrations of REE at 70C

    SciTech Connect

    Gary Garland

    2015-06-29

    This dataset shows the sorption capacities of smaller grain size (-50 +100 mesh) of media #1 in brine #1 at different starting concentrations of REE's at elevated temperature of 70C. The experimental conditions are 2g of -50 +100 mesh media #1 to 150mL of REE solution at concentartions of .2ppm each, 2ppm each, and 20ppm each. The pH of the solution is 5.5, and the temperature was at 70C.

  18. High-Pressure Rare Earth Disilicates REE2Si 2O 7( REE=Nd, Sm, Eu, Gd): Type K

    NASA Astrophysics Data System (ADS)

    Fleet, Michael E.; Liu, Xiaoyang

    2001-10-01

    A new structure type (K) is reported for the disilicates of Nd, Sm, Eu, and Gd made at high pressure. Crystals of type K were synthesized at 10 GPa, 1600-1700°C in an MA6/8 superpress and used for single-crystal X-ray structure study by Kappa CCD diffractometry at room temperature. Crystal data are: monoclinic, space group P21/n, Z=4; Nd2Si2O7-a=6.6658(2), b=6.7234(3), c=12.3975(6) Å, β=102.147(3)°, V=543.2 Å3, R=0.029, and Dx=5.584 g/cm3; Sm2Si2O7-a=6.6039(3), b=6.6849(3), c=12.3069(5) Å, β=102.489(3)°, V=530.4 Å3, R=0.038, and Dx=5.871 g/cm3; Eu2Si2O7-a=6.5777(3), b=6.6652(4), c=12.2668(8) Å, β=102.671(4)°, V=524.7 Å3, R=0.030, and Dx=5.976 g/cm3; Gd2Si2O7-a=6.5558(4), b=6.6469(4), c=12.2394(6) Å, β=102.844(3)°, V=520.0 Å3, R=0.026, and Dx=6.166 g/cm3. The type K structure is built from a diorthosilicate group [Si2O7] interconnected by REE3+ cations in eightfold coordination with oxygen. The bridging oxygen (Si-O-Si) bond angle of the diorthosilicate group of rare earth disilicates stable at 1 bar (types A to G) is related to spatial accommodation of the REE3+ cation and ranges from 130 to 135° in the light rare earth disilicates (types A, F, G) to 180° in Lu2Si2O7 (type C). Volume reduction in the high-pressure type K structure is achieved largely by closure of the Si-O-Si bond angle to 122.7-124.4°, through rigid body rotation of the two SiO4 tetrahedra. This also permits a marginal increase in the average coordination of the REE3+ cation.

  19. High REE and Y concentrations in Co-Cu-Au ores of the Blackbird district, Idaho

    USGS Publications Warehouse

    Slack, J.F.

    2006-01-01

    Analysis of 11 samples of strata-bound Co-Cu-Au ore from the Blackbird district in Idaho shows previously unknown high concentrations of rare earth elements (REE) and Y, averaging 0.53 wt percent ???REE + Y oxides. Scanning electron microscopy indicates REE and Y residence in monazite, xenotime, and allanite that form complex intergrowths with cobaltite, suggesting coeval Co and REE + Y mineralization during the Mesoproterozoic. Occurrence of high REE and Y concentrations in the Blackbird ores, together with previously documented saline-rich fluid inclusions and Cl-rich biotite, suggest that these are not volcanogenic massive sulfide or sedimentary exhalative deposits but instead are iron oxide-copper-gold (IOCG) deposits. Other strata-bound Co deposits of Proterozoic age in the North American Cordillera and elsewhere in the world may have potential for REE and Y resources. IOCG deposits with abundant light REE should also be evaluated for possible unrecognized heavy REE and Y mineralization. ?? 2006 by Economic Geology.

  20. Trace element and REE geochemistry of Red Butte, Oregon: a gold-bearing hot spring system

    SciTech Connect

    Evans, C.S.; Cummings, M.L.

    1985-01-01

    Red Butte, 60 km south of Vale, Oregon is an Au-bearing hot spring deposit of intercalated lacustrine and fluvial Mio-Pliocene volcaniclastic sediments and basalt flows. Topography of the butte is controlled by a 30-60 m thick cap of silicified sediments which is cut by N and NW-trending faults. Anomalous Au, As, Sb, and Hg occur in fault controlled quartz veins, quartz-adularia veins, silicified sediments and rarely in calcite-quartz veins cutting basalt. Distribution of these elements away from the veins is controlled by permeability of the host rock. REE concentrations were normalized to chondritic abundances for 73 sediment, basalt, and vein samples. Silicified sediments from the butte top and unsilicified sediments from the east slope of the butte have similar LREE enriched patterns with strong negative Eu anomalies reflecting their felsic volcanic source. Silicified sediments are depleted in all REEs relative to fresh sediments indicating dilution by silica deposition. Basalt REE patterns are much closer to chondritic ratios. Patterns of veined basalt mirror those for fresh basalts but are relatively depleted in all REEs. Quartz-adularia and quartz veins have REE abundances 2-3 orders of magnitude lower than fresh sediments, and REE patterns unlike either the sediments or basalts. Mobility of REEs in the hydrothermal fluid is seen in La/Sm and Sa/Yb ratios of the veins. The La/Sm ratio for sediments averages 3.70. In veins this ratio drops to 1.65. The average La/Yb ratio is 9.1 in sediments and falls to 1.65 in quartz veins. Fluids depositing quartz and adularia in veins carried REEs in low abundance and deposited them in ratios that do not reflect the host rock. Any movement of REEs in host rock may have been masked by original high REE content combined with silica dilution.

  1. Experimental mineral/liquid partition coefficients of the rare earth elements /REE/, Sc and Sr for perovskite, spinel and melilite

    NASA Technical Reports Server (NTRS)

    Nagasawa, H.; Schreiber, H. D.; Morris, R. V.

    1980-01-01

    Experimental determinations of the mineral/liquid partition coefficients of REE (La, Sm, Eu, Gd, Tb, Yb and Lu), Sc and Sr are reported for the minerals perovskite, spinel and melilite in synthetic systems. Perovskite concentrates light REE with respect to the residual liquid but shows no preference for heavy REE. Spinel greatly discriminates against the incorporation of REE, especially light REE, into its crystal structure. The partition of REE into melilite from a silicate liquid is quite dependent upon both the bulk melt and melilite solid-solution (gehlenite and akermanite components) compositions. As such, melilite can be enriched in REE or will reject REE with corresponding strong negative or strong positive Eu anomalies, respectively.

  2. Some Remarks on the Interpretation of the REE-in-two-Mineral Thermobarometers

    NASA Astrophysics Data System (ADS)

    Sun, C.; Liang, Y.; Yao, L.; Dygert, N. J.; Wang, C.

    2015-12-01

    Distributions of REE between mantle minerals depend on temperature, pressure and mineral compositions, and can be used as thermobarometers. We have developed a REE-in-two-pyroxene thermometer, a REE-in-garnet-clinopyroxene thermobarometer, and a REE-in-plagioclase-augite thermometer for ultramafic and mafic rocks. These trace element based two-mineral thermobarometers are built on parameterized lattice strain models for mineral-melt REE partitioning that we independently calibrated using published data from mineral-melt partitioning experiments. The physical meanings of calculated temperatures and pressures can be understood in terms of the average closure temperatures and closure pressures of REE in cooling bi-mineralic systems. Because trivalent REE diffuse slower than divalent Ca-Fe-Mg in minerals, the REE-based thermobarometers may record early thermal event(s), whereas the major element based thermometers may record more recent thermal events in closed systems that experienced cooling. A number of geological and geodynamic processes can result in decreases in temperature and possibly pressure over time: mantle upwelling beneath mid-ocean ridge spreading centers or in response to lower crust delamination, exhumation, heat loss to country rock from crustal magma chambers. For shallow level intrusive or extrusive mafic rocks, temperatures derived from the REE-in-plagioclase-augite thermometer may correspond to plagioclase saturation temperature. Hence application of REE- and Ca-Fe-Mg based thermobarometers to the same samples can shed new insight into the thermal history of mafic and ultramafic rocks. Initial applications of the REE-in-two-mineral thermobarometers to Earth and planetary samples have lead to a number of interesting observations which we will summarize in this presentation. However, care and caution must be exercised when processing and interpreting data from REE-in-two-mineral thermobarometers. Common issues include inaccuracies in REE data

  3. Heterogeneous rare earth element (REE) patterns and concentrations in a fossil bone: Implications for the use of REE in vertebrate taphonomy and fossilization history

    NASA Astrophysics Data System (ADS)

    Suarez, Celina A.; Macpherson, G. L.; González, Luis A.; Grandstaff, David E.

    2010-05-01

    A bone fragment (CGDQ-3) of Falcariusutahensis, a therizinosaur from the Early Cretaceous Cedar Mountain Formation, Utah, contained within a carbonate nodule, was analyzed by laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) in order to investigate REE variability within a thin-walled phalanx. Previous studies have found depth-related REE pattern variations; however, in CGDQ-3 variation occurs along the circumference of the bone. NASC-normalized REE patterns and concentrations vary between two apparent end members. A light-REE enriched (LREE) pattern, similar to solution ICP-MS analysis of this bone, characterizes approximately two-thirds of the bone fragment. Total REE concentrations are high and do not vary significantly from the periosteal surface to the medullar surface. Conversely, the remaining one-third of the bone has REE patterns that are MREE-depleted and low in total REE concentrations. REE concentrations in this part of the bone do not vary significantly from the periosteal to the medullar surface. A positive Ce anomaly is found throughout the entire bone, and is greatest within the LREE-enriched portion of the bone. This, in combination with the LREE-enrichment, suggests that the bone fossilized under reducing conditions. The distance between the LREE-enriched and MREE-depleted regions is less than 1 mm. Isotopic and petrographic analyses of the bone and surrounding carbonate matrix suggest the REE patterns in the bone were the result of partial fossilization/incomplete filling of micro-pore spaces around bone crystallites in an environment with changing redox conditions. The lower, MREE-depleted part of the bone fossilized contemporaneously with a pendant cement that formed on the underside of the bone in the vadose zone. Formation of the pendant cement restricted water flow through the bone, isolating the lower portion, which incorporated a MREE-depleted pattern. The upper part of the bone (LREE-enriched side) fossilized under

  4. Duality and genetic significance of REE speciation in tourmaline from tin deposits of the Far East

    NASA Astrophysics Data System (ADS)

    Gorelikova, N. V.; Balashov, F. V.; Bychkova, Ya. V.; Minervina, E. A.; Korostelev, P. G.; Magazina, O. L.; Bortnikov, N. S.

    2016-04-01

    The distribution of REEs and some minor elements in tourmalines of different associations and deposits of the Russian Far East is studied by the methods of ICP-MS, ICP-MS with laser ablation and scanning electron microscopy. The duality of REE speciation in tourmaline is established: in high-temperature varieties, most REEs (mainly HREEs) are incorporated in rare minerals (monazite, xenotime, zircon, and F-Ce-Y carbonate), whereas hydrothermal ores are characterized by isomorphic incorporation of LREEs in the mineral structure, as well as by a fine admixture of zircon at the expense of detrital clasts in flyschoid rocks with the zones of tourmalinization.

  5. Origin of REE mineralization in the Bastnäs-type Fe-REE-(Cu-Mo-Bi-Au) deposits, Bergslagen, Sweden

    NASA Astrophysics Data System (ADS)

    Holtstam, Dan; Andersson, Ulf B.; Broman, Curt; Mansfeld, Joakim

    2014-09-01

    The Bastnäs-type deposits, with mineral assemblages of Fe oxides, Ca-Mg silicates, rare earth element (REE) silicates, REE fluorocarbonates, and Cu-Fe-Mo-Bi sulfides, are associated with marble horizons in a strongly Na, K, and/or Mg altered, metavolcanic succession, over a distance of at least 80 km in a SW-NE trending zone in western Bergslagen. Two subtypes occur: (1) enriched (relative to the other type) in light REE (LREE) and Fe, exemplified by the Bastnäs and Rödbergsgruvan deposits, and (2) enriched in heavy REE (HREE), Y, Mg, Ca, and F, represented by deposits in the Norberg district. Bastnäsite hosts primary fluid H2O-CO2 inclusions with salinities of 6-29 eq. wt% CaCl2 and with total homogenization temperatures (Th tot) of ca. 300-400 °C. Subtype 2 has late-stage fluorite with fluid inclusions that show 1-16 eq. wt% NaCl and Th tot of ca. 90-150 °C. Molybdenite Re-Os ages obtained from three deposits are 1,904 ± 6, 1,863 ± 4, and 1,842 ± 4 Ma. Nd isotopic data from five different REE minerals yielded no defined isochron, but a range in ɛNd (1.88 Ga) of +0.2 to +1.6. The oxygen isotope values (δ18OSMOW) of dolomite and calcite from the associated REE-mineralized skarn and recrystallized carbonate assemblages lie in the range 6.1-8.6 ‰, overlapping with those of the host marbles. Carbon isotope values (δ13CPDB) show typical magmatic signatures of -6.7 to -4.4 ‰, while the host marbles group around ca. -2.4 ‰. The sulfur isotope (δ34SCDT) values of associated sulfides range between -10.8 and +0.2 ‰. The combined evidence suggests REE mineralization, beginning at 1.9 Ga, from mainly Svecofennian, juvenile magmatic (>400 °C) fluids carrying Si, F, Cl, S, CO2, and the REE in addition to other metals; mineralization occurred through reactions with dolomitic layers in the supracrustal units coevally with regional metasomatic alteration associated with fluid circulation through an extensive active volcano-plutonic complex.

  6. Origin of REE mineralization in the Bastnäs-type Fe-REE-(Cu-Mo-Bi-Au) deposits, Bergslagen, Sweden

    NASA Astrophysics Data System (ADS)

    Holtstam, Dan; Andersson, Ulf B.; Broman, Curt; Mansfeld, Joakim

    2014-12-01

    The Bastnäs-type deposits, with mineral assemblages of Fe oxides, Ca-Mg silicates, rare earth element (REE) silicates, REE fluorocarbonates, and Cu-Fe-Mo-Bi sulfides, are associated with marble horizons in a strongly Na, K, and/or Mg altered, metavolcanic succession, over a distance of at least 80 km in a SW-NE trending zone in western Bergslagen. Two subtypes occur: (1) enriched (relative to the other type) in light REE (LREE) and Fe, exemplified by the Bastnäs and Rödbergsgruvan deposits, and (2) enriched in heavy REE (HREE), Y, Mg, Ca, and F, represented by deposits in the Norberg district. Bastnäsite hosts primary fluid H2O-CO2 inclusions with salinities of 6-29 eq. wt% CaCl2 and with total homogenization temperatures ( Th tot) of ca. 300-400 °C. Subtype 2 has late-stage fluorite with fluid inclusions that show 1-16 eq. wt% NaCl and Th tot of ca. 90-150 °C. Molybdenite Re-Os ages obtained from three deposits are 1,904 ± 6, 1,863 ± 4, and 1,842 ± 4 Ma. Nd isotopic data from five different REE minerals yielded no defined isochron, but a range in ɛNd (1.88 Ga) of +0.2 to +1.6. The oxygen isotope values (δ18OSMOW) of dolomite and calcite from the associated REE-mineralized skarn and recrystallized carbonate assemblages lie in the range 6.1-8.6 ‰, overlapping with those of the host marbles. Carbon isotope values (δ13CPDB) show typical magmatic signatures of -6.7 to -4.4 ‰, while the host marbles group around ca. -2.4 ‰. The sulfur isotope (δ34SCDT) values of associated sulfides range between -10.8 and +0.2 ‰. The combined evidence suggests REE mineralization, beginning at 1.9 Ga, from mainly Svecofennian, juvenile magmatic (>400 °C) fluids carrying Si, F, Cl, S, CO2, and the REE in addition to other metals; mineralization occurred through reactions with dolomitic layers in the supracrustal units coevally with regional metasomatic alteration associated with fluid circulation through an extensive active volcano-plutonic complex.

  7. Mineral recorders of pegmatite internal evolution: REE contents of tourmaline from the Bob Ingersoll pegmatite, South Dakota

    SciTech Connect

    Jolliff, B.L.; Papike, J.J.

    1987-08-01

    Trace rare earth elements (REE) have been determined by radiochemical neutron activation analysis for tourmaline samples from an internally zoned, rare-element, granitic pegmatite, located in the Black Hills, South Dakota. The Total REE concentrations range from 40 ppm-0.2 ppm, and are highest in tourmaline from the exomorphic halo (country rock) and pegmatite border zone. Chondrite-normalized patterns are highly fractionated from light REE to heavy REE; and REE concentrations decrease in tourmaline from the outer wall zone and first intermediate zone, through the inner wall zone and third intermediate zone, to lowest levels in the pegmatite core. The REEs, as recorded by tourmaline, appear to behave compatibly in this pegmatite system due to early crystallization of apatite and other possible REE-sink minerals. The large range of REE concentrations and differences in slopes of chondrite-normalized patterns probably also reflect significant changes in the structural state of the pegmatite melt, caused by changes in pH/sub 2/O and other volatiles (B, F, P) as crystallization progressed. Tourmaline samples that appear to have been fluid-derived are HREE-depleted relative to coexisting silicate-melt-derived tourmaline. Tourmaline does not exhibit any strong preference for specific REEs, rather its REE content appears to reflect the REE content of the medium from which the tourmaline crystallized.

  8. Cancer vaccines: looking to the future. Interview by Jenaid Rees.

    PubMed

    Apostolopoulos, Vasso

    2013-10-01

    Interview by Jenaid Rees (Commissioning Editor) Vasso Apostolopoulos has been working in the field of cancer vaccines since 1991, and human clinical trials on her work have been conducted since 1994. Her work has been at the forefront of scientific research into the development of a vaccine for cancer and she has received over 90 awards and honours in recognition of her achievements. Some notable awards include, the Premier's Award for medical research, was named Young Australian of the Year (Victoria), recipient of the Channel 10/Herald Sun Young Achiever of the Year Award as well as being awarded the Order of Brigadier General of the Phoenix Battalion by the Greek President. In 1998 Apostolopoulos received the NHMRC CJ Martin Research Fellowship and worked at the Scripps Research Institute in California, USA, for 3.5 years and returned to the Austin Research Institute (VIC, Australia), and headed the Immunology and Vaccine Laboratory receiving the NHMRC RD Wright Fellowship. Upon her return to Australia, Apostolopoulos received the Victorian Tall Poppy Award, the Bodossaki Foundation Academic Prize, was inducted into the Victorian Honour roll of Women, was a torchbearer for the Melbourne leg of the International Athens 2004 Olympic Torch Relay, was named Woman of the Year, and is an Australia Day Ambassador. Her contribution into cancer research, vaccines and immunology has been extensive - publishing over 200 scientific papers and books, an inventor on 14 patents and collaborates with over 50 national and international Research Institutes and Universities. Her current research interests are in the development of new improved cancer vaccines and new modes of antigen delivery for immune stimulation. She is also interested in chronic diseases treatment and prevention through immunotherapy. She serves on the Editorial Board for Expert Review of Vaccines. PMID:24093953

  9. Chemical characteristic of R chondrites in the light of P, REEs, Th and U abundances

    NASA Astrophysics Data System (ADS)

    Khan, Rahat; Shirai, Naoki; Ebihara, Mitsuru

    2015-07-01

    Rare earth elements (REEs), Th, U and P were determined in 15 Rumuruti (R)-type chondrites and the Allende CV chondrite. Repeated analyses of Allende for REEs, Th and U by ICP-MS and P by ICP-AES, and comparisons of these data with literature values ensure high reproducibility (precision) and reliability (accuracy) of acquired data. CI-normalized REE abundances in R chondrites are slightly enriched in heavy REEs with a small, positive Ce anomaly, in contrast to Allende. CI-normalized Pr/Tm and Nd/Yb ratios show a positive correlation, suggesting the heterogeneous mixing of two components (CI-like and refractory-rich materials) during the accretion of the R chondrite parent body. A Ce anomaly, however, was likely homogeneously present in the nebula. A mean Th/U ratio of R chondrites is 3.81 ± 0.13 (1 σ), which is 5.1% higher than the CI ratio. Probably, the Th-U fractionation was inherited from the nebula from which the R chondrite parent body formed. Besides the Th-U fractionation, REEs and Th-U are heterogeneously fractionated in R chondrites, for which parent body processing is assumed to be the cause. A mean P content of R chondrites (1254 μg/g) is higher than for any ordinary chondrite and is close to the EL mean. There appears to be a negative correlation between P and REEs contents in R chondrites. It is probable that REEs were diluted by extraneously supplied, REEs-depleted and P-containing materials (schreibersite or metal). This process must have occurred heterogeneously during accretion so that the heterogeneity of P-containing materials was preserved in the R chondrite parent body and individual R chondrites.

  10. The influence of solution chemistry on REE uptake by Ulva lactuca L. in seawater

    NASA Astrophysics Data System (ADS)

    Stanley, John K., Jr.; Byrne, Robert H.

    1990-06-01

    Simultaneous uptake of Ce(III), Eu(III), Gd(III), Yb(III), and Zn(II) by an organic substrate, Ulva lactuca L., was examined in seawater. REE behavior was observed to be strongly dependent on solution complexation. Over a range of carbonate ion concentrations between 10 -6 mol kg-soln -1 and 7 × 10 -3 mol kg-soln -1, the affinity of Ulva lactuca for Gd(III) decreased by approximately two orders of magnitude. The influence of carbonate complexation on REE solid/solution distributions was much larger for Yb(III) than for Gd(III) and was larger for Gd(III) than for Ce(III). At carbonate ion concentrations greater than about 6 × 10 -5molkg- soln-1, REE solid/solution partition coefficients, DT( M) = ( REEactivityg-1Ulva)/( REEactivityg-1seawater) exhibited the order Ce(III) > Eu(III) > Gd(III) > Yb(III). At carbonate ion concentrations less than about 3 × 10 =-5molkg- soln-1, the affinity of Ulva lactuca L. for REEs exhibited the order Eu( III) > Gd( III) > Ce( III) > Yb( III). Our partition coefficient observations are in general accord with shale-normalized REE abundance patterns in seawater. Adsorption by organic substrates can produce heavy REE enrichments in seawater relative to the LREEs, Gd(III) solution enrichments relative to Eu(III), and, at relatively low carbonate ion concentrations, enrichments of very light REEs compared to their immediate neighbors. The behavior of Zn(II) in our study differed considerably from the REEs. The partition of Zn(II) between Ulva and seawater is not strongly dependent on carbonate ion concentration.

  11. REE Behavior During Anhydrite and Gypsum Formations of the Kuroko Type Massive Sulfide-Sulfate Deposits

    NASA Astrophysics Data System (ADS)

    Ogawa, Yasumasa; Shikazono, Naotatsu

    2006-05-01

    The Sr and rare earth elements (REEs) concentrations and Sr isotopic composition (87Sr/86Sr) of anhydrite and gypsum have been determined for samples from the Matsumine, Shakanai and Hanaoka Kuroko-type massive sulfide-sulfate deposits in the Hokuroku District in Akita Pref. in northern Japan. The anhydrite samples exhibit two styles of chondrite-normalized REE patterns; one with a decrease from light to heavy REEs (Type I), and another with a light REE-depleted pattern with peak in Sm (Type II). The Sr content of Type I anhydrite is higher than that of Type II. The 87Sr/86Sr ratios of all anhydrite samples are intermediate between that of middle Miocene seawater and that of country rocks. 87Sr/86Sr of Type I anhydrite is closer to Miocene seawater, and that of Type II is closer to the country rocks. Based on the Sr data obtained by this study and previous reports on geochemical data on the Kuroko mineralization, geochemical environment of anhydrite formation was investigated. However, from that investigation, it is inferred that REE fractionation would not occur during the primary anhydrite precipitation. Gypsum, which partially replaces anhydrite in the Kuroko deposits, also exhibits two distinct chondrite-normalized REE patterns. Because LREEs are likely to be more easily mobilized during the secondary process such as dissolution and re-crystallization, it is hypothesized that LREE release from Type I anhydrite, resulting in the formation of secondary Type II anhydrite with LREE depleted profiles.

  12. Rare earth elements (REEs) in the tropical South Atlantic and quantitative deconvolution of their non-conservative behavior

    NASA Astrophysics Data System (ADS)

    Zheng, Xin-Yuan; Plancherel, Yves; Saito, Mak A.; Scott, Peter M.; Henderson, Gideon M.

    2016-03-01

    This study presents new concentration measurements of dissolved rare earth elements (dREEs) along a full-depth east-west section across the tropical South Atlantic (∼12°S), and uses these data to investigate the oceanic cycling of the REEs. Enrichment of dREEs, associated with the redox cycling of Fe-Mn oxides, is observed in the oxygen minimum zone (OMZ) off the African shelf. For deeper-waters, a multi-parameter mixing model was developed to deconvolve the relative importance of physical transport (i.e., water mass mixing) from biogeochemical controls on the dREE distribution in the deep Atlantic. This approach enables chemical processes involved in REE cycling, not apparent from the measurements alone, to be distinguished and quantified. Results show that the measured dREE concentrations below ∼1000 m are dominantly controlled (>75%) by preformed REE concentrations resulting from water mass mixing. This result indicates that the linear correlation between dREEs and dissolved Si observed in Atlantic deep waters results from the dominantly conservative behavior of these tracers, rather than from similar chemical processes influencing both dREEs and Si. Minor addition of dREEs (∼10% of dNd and ∼5% of dYb) is observed in the deep (>∼4000 m) Brazil Basin, resulting from either remineralization of particles in-situ or along the flow path. Greater addition of dREEs (up to 25% for dNd and 20% for dYb) is found at ∼1500 m and below ∼4000 m in the Angola Basin near the African continental margin. Cerium anomalies suggest that different sources are responsible for these dREE addition plumes. The 1500 m excess is most likely attributed to dREE release from Fe oxides, whereas the 4000 m excess may be due to remineralization of calcite. Higher particulate fluxes and a more sluggish ocean circulation in the Angola Basin may explain why the dREE excesses in this basin are significantly higher than that observed in the Brazil Basin. Hydrothermal venting over the

  13. Comparison of fluorite geochemistry from REE deposits in the Panxi region and Bayan Obo, China

    NASA Astrophysics Data System (ADS)

    Xu, Cheng; Taylor, Rex N.; Li, Wenbo; Kynicky, Jindrich; Chakhmouradian, Anton R.; Song, Wenlei

    2012-09-01

    Panxi region in west Sichuan province is one of the most economically significant REE mineralization belts in China, and includes the large Maoniuping and Daluxiang deposits and the minor Lizhuang deposit. The REE mineralization in these deposits is spatially and temporally associated with carbonatite-syenite complexes. Large proportional fluorites and REE minerals occurring as veins intrude Cretaceous granite and Oligocene syenite in Maoniuping, and Oligocene syenite and carbonatite in Lizhuang, and Miocene syenite in Daluxiang. Fluorite is also one of main gangue minerals in the world-class Bayan Obo REE deposit. We present a comparison of the trace element and isotopic compositions of fluorites from four REE deposits in the Panxi region and Bayan Obo. The fluorites from Maoniuping and Daluxiang are characterized by variable REE patterns, with either LREE enrichment or LREE depletion relative to MREE. Typically they have a larger range in La/Ho compared to Y/Ho ratios, and pronounced positive Y anomaly relative to chondrite-normalized REE patterns. Their REE distribution patterns are controlled by fluoride-complexes and the loss of separate LREE-rich minerals. Different Y/Ho (ca. 73 vs. 108) and initial Sr isotopic (ca. 0.7061 vs. 0.7077) ratios are observed between the fluorites from Maoniuping and Daluxiang, reflecting their different source compositions. This contrasts with the fluorites from Maoniuping and Lizhuang, which have similar initial Sr isotopes, and appear to be cogenetic. However, the Lizhuang fluorite shows a consistent depletion of LREE relative to MREE, as well as lower Y/Ho ratios and higher HREE content than that in Maoniuping. In this respect the Lizhuang fluorite may have precipitated from a late-stage fluid following abundant fluorite and REE mineral deposition in Maoniuping. Carbonate, more than fluoride complexing, appears to have a stronger control on REE fractionation in the Lizhuang fluorites. The fluorites from three deposits in Panxi

  14. REE mineralization in the carbonatites of the sung valley ultramafic-alkaline-carbonatite complex, Meghalaya, India

    NASA Astrophysics Data System (ADS)

    Sadiq, Mohd.; Ranjith, A.; Umrao, Ravi

    2014-12-01

    The Early Cretaceous Sung Valley Ultramafic-Alkaline-Carbonatite (SUAC) complex intruded the Proterozoic Shillong Group of rocks and located in the East Khasi Hills and West Jaintia Hills districts of Meghalaya. The SUAC complex is a bowl-shaped depression covering an area of about 26 km2 and is comprised serpentinised peridotite forming the core of the complex with pyroxenite rim. Alkaline rocks are dominantly ijolite and nepheline syenite, occur as ring-shaped bodies as well as dykes. Carbonatites are, the youngest intrusive phase in the complex, where they form oval-shaped bodies, small dykes and veins. During the course of large scale mapping in parts of the Sung Valley complex, eleven carbonatite bodies were delineated. These isolated carbonatite bodies have a general NW-SE and E-W trend and vary from 20-125 m long and 10-40 m wide. Calcite carbonatite is the dominant variety and comprises minor dolomite and apatite and accessory olivine, magnetite, pyrochlore and phlogopite. The REE-bearing minerals identified in the Sung Valley carbonatites are bastnäsite-(Ce), ancylite-(Ce), belovite-(Ce), britholite-(Ce) and pyrochlore that are associated with calcite and apatite. The presence of REE carbonates and phosphates associated with REE-Nb bearing pyrochlore enhances the economic potential of the Sung Valley carbonatites. Trace-element geochemistry also reveals an enrichment of LREEs in the carbonatites and average ΣREE value of 0.102% in 26 bed rock samples. Channel samples shows average ΣREE values of 0.103 wt%. Moreover, few samples from carbonatite bodies has indicated relatively higher values for Sn, Hf, Ta and U. Since the present study focuses surface evaluation of REE, therefore, detailed subsurface exploration will be of immense help to determine the REE and other associated mineralization of the Sung Valley carbonatite prospect.

  15. Temporal variations in the export of REE in boreal catchments of varying character and size

    NASA Astrophysics Data System (ADS)

    Köhler, S.; Lidman, F.; Mörth, M.; Björkvald, L.; Laudon, H.

    2009-04-01

    Organic matter and iron colloids have a large impact on the mobilisation of trivalent elements such as aluminium (Al), rare earth elements (REE) and actinides. Recent results of the relative importance of these colloids are diverging though (POURRET et al., 2007); STEINMANN and STILLE, 2008) and there is a general lack of information of the importance of flow pathways and landscape type on the relative importance of the various colloidal fractions that mobilizes REE from the catchment soils. In this study we present the data of water chemical analysis of a series of catchments with varying size and character but all within the boreal zone. Two speciation techniques and two column separation methods involving ion exchange were used to quantify the causes for the temporal variation of the dissolved amounts of trivalent ions in these water courses. Our study indicates that REE export is controlled mostly by landscape type while changes in the acid-base character of organic matter are of minor importance. Changes in flow pathways in a riparian zone in one of the studied areas in a forested site may be used to decipher the effect of chemical versus physical processes for the mobilisation of REE and aluminium and open up the possibility for a quantitative modelling of the varying sources of REE. Iron and aluminium are mobilized together with organic matter in varying amounts in different landscape types and this affects the REE export from the various landscape elements. While the amount of strongly bound aluminium mobilized from the catchments usually correlate positively with any of the REE this is not the case for strongly bound iron. Fractionation patterns of REE are discussed and the observed binding of REE to organic matter was modelled using the speciation program WHAM VI (TIPPING, 1998). Pourret O., Davranche M., Gruau G., and Dia A. (2007) Organic complexation of rare earth elements in natural waters: Evaluating model calculations from ultrafiltration data

  16. Heterovalent substitutions in garnet and their implications for diffusion of Y+REEs and alkalis (Invited)

    NASA Astrophysics Data System (ADS)

    Carlson, W. D.; Gale, J. D.; Wright, K.

    2013-12-01

    Lattice-dynamics calculations in the static limit suggest that large trivalent ions (Y+REEs) are incorporated into garnet primarily by means of substitutions that introduce menzerite and alkali components. The diffusion mechanisms implied by this finding explain otherwise puzzling aspects of recent determinations of diffusion rates for Y+REEs and Li in natural systems, bolstering confidence in the validity of those rates. Several substitution schemes have been proposed to provide the charge-balance required for incorporation of trivalent Y+REEs substituting for divalent cations in dodecahedral sites in aluminosilicate garnet: (1) YAG components, with tetrahedral Al; (2) vacancy components, with one unoccupied dodecahedral site for each two trivalent ions; (3) alkali components, with dodecahedral Na or Li; (4) menzerite components, with octahedral Mg or Fe; and (5) Y2Li components, with octahedral Li compensating for a pair of Y+REE ions. The relative energetic costs of these substitutions were evaluated in pyrope, almandine, spessartine and grossular by means of lattice-dynamics calculations at T = 0 K and P = 0 GPa, using well-established force-field potentials, and referencing exchange energies to the lattice energies of binary oxides as sources/sinks for the exchanged ions. Energies calculated for the incorporation of menzerite and alkali components are appreciably lower than those for the YAG component, and very substantially lower than those for the other components. Provided that the relative energetic costs are similar at elevated T and P to those in the static limit (testing of this assumption is currently underway), the menzerite and alkali substitutions should predominate in natural aluminosilicate garnets, the YAG substitution should play only a subordinate role, and the other substitutions should be near-negligible. As a result, diffusion mechanisms for Y+REEs in garnet require that motion of these elements must be coupled to transport of either

  17. Formation of the world's largest REE deposit through protracted fluxing of carbonatite by subduction-derived fluids

    PubMed Central

    Ling, Ming-Xing; Liu, Yu-Long; Williams, Ian S.; Teng, Fang-Zhen; Yang, Xiao-Yong; Ding, Xing; Wei, Gang-Jian; Xie, Lu-Hua; Deng, Wen-Feng; Sun, Wei-Dong

    2013-01-01

    Rare Earth Elements (REE) are essential to modern society but the origins of many large REE deposits remain unclear. The U-Th-Pb ages, chemical compositions and C, O and Mg isotopic compositions of Bayan Obo, the world's largest REE deposit, indicate a protracted mineralisation history with unusual chemical and isotopic features. Coexisting calcite and dolomite are in O isotope disequilibrium; some calcitic carbonatite samples show highly varied δ26Mg which increases with increasing Si and Mg; and ankerite crystals show decreases in Fe and REE from rim to centre, with highly varied REE patterns. These and many other observations are consistent with an unusual mineralisation process not previously considered; protracted fluxing of calcitic carbonatite by subduction-released high-Si fluids during the closure of the Palaeo-Asian Ocean. The fluids leached Fe and Mg from the mantle wedge and scavenged REE, Nb and Th from carbonatite, forming the deposit through metasomatism of overlying sedimentary carbonate.

  18. Mobilization and redistribution of REEs and thorium in a syenitic lateritic profile: A mass balance study

    SciTech Connect

    Braun, J.J.; Pagel, M.; Herbillon ); Rosin, C. )

    1993-09-01

    REE-Th geochemistry and mineralogy have been studied in a lateritic profile derived from a syenite at Akongo in SW Cameroon. REE and Th mass balance calculations for the host-rock minerals show that at least 70% of the LREEs and 50% of the HREEs are contained in allanite, apatite, titanite, and epidote and at least 50% of the Th is controlled by the same accessory materials which represent about 2 wt% of the unaltered syenite. These accessory phases are destroyed during the first stages of weathering causing most of the REEs and Th to be rapidly released into the soil. Comparison of the variation in the Zr, Ti, and Th content as a function of the apparent density of the different zones of the saprolite shows that Th is the least mobile element. The presence of secondary thorianite (ThO[sub 2]), the etched surface on zircon grains, and the presence of Ti in secondary cerianite support this geochemical interpretation. The concentration of thorium was, therefore, chosen as invariant relative to the concentration of the other elements, especially the REEs, in mass balance calculations. Most of the REEs are leached in the iron-rich upper horizons (loose nodular horizon, iron crust, and top of mottled clay horizon). Where the groundwater table moves (saprolite and bottom of the mottled clay horizon), the REEs are fractionated and redistributed. There is a juxtaposition of leached and accumulation zones with precipitation of LREE aluminous hydrated phosphates. This study supports the existence of two different cycles for the redistribution of elements in the soil: (1) as dissolved ions in the saprolite horizon, and (2) as individual particles in the upper part of the profile.

  19. Ion microprobe U-Pb dating and REE abundance of biogenic apatite

    NASA Astrophysics Data System (ADS)

    Sano, Y.; Terada, K.; Ueki, S.

    2001-12-01

    If the direct U-Pb dating of a fossil itself is possible, the method could have great impact on stratigraphic studies in establishing the absolute chronology of sedimentary sequences. Micro fossil ?conodont? are candidates for this purpose since they consist of apatite (Ca2(PO5)3 (F,Cl,OH)), which would uptake U, Th and Pb after sedimentation no longer than a few million years and is supposed to remain closed to U and Pb under relatively low effective closure temperature. We report here results of direct ion microprobe U-Th-Pb dating of two conodonts; Trichognathus from Kinderhookian stage of Mississippian sedimentary sequence from Illinois Basin region in North America and Panderodus from a Llandoverian sedimentary sequence on Langkawi Island, northern Malaysia. Secondary purpose of the study is to indicate in situ analysis of all REE on the same spots of U-Pb measurements. Samples were cast into epoxy resin discs with a few grains of standard apatite, PRAP, derived from an alkaline rock of Prairie Lake circular complex in the Canadian Shield and polished until they were exposed through their mid-sections. U, Th and REE abundances, and Pb isotopic compositions were measured by using SHRIMP installed at Hiroshima University. Thirteen spots on Trichognathus yield a 238U/206Pb isochron age of 323+/-36 Ma, which is consistent with the depositional and early diagenetic ages. Fifteen spots on Panderodus give 232Th/208Pb isochron age of 429+/-50 Ma, which is again comparable to an early Silurian. Shale-normalized REE of Trichognathus shows a broadly flat pattern from light to middle REE and a decrease from middle to heavy REE with negative anomalies of Ce and Eu. In contrast Panderodus indicates a concave-shape pattern with middle REE enrichment. These characteristics are probably due to a different formation environment as suggested by other workers.

  20. Rare earth elements (REEs): effects on germination and growth of selected crop and native plant species.

    PubMed

    Thomas, Philippe J; Carpenter, David; Boutin, Céline; Allison, Jane E

    2014-02-01

    The phytotoxicity of rare earth elements (REEs) is still poorly understood. The exposure-response relationships of three native Canadian plant species (common milkweed, Asclepias syriaca L., showy ticktrefoil, Desmodium canadense (L.) DC. and switchgrass, Panicum virgatum L.) and two commonly used crop species (radish, Raphanus sativus L., and tomato, Solanum lycopersicum L.) to the REEs lanthanum (La), yttrium (Y) and cerium (Ce) were tested. In separate experiments, seven to eight doses of each element were added to the soil prior to sowing seeds. Effects of REE dose on germination were established through measures of total percent germination and speed of germination; effects on growth were established through determination of above ground biomass. Ce was also tested at two pH levels and plant tissue analysis was conducted on pooled samples. Effects on germination were mostly observed with Ce at low pH. However, effects on growth were more pronounced, with detectable inhibition concentrations causing 10% and 25% reductions in biomass for the two native forb species (A. syriaca and D. canadense) with all REEs and on all species tested with Ce in both soil pH treatments. Concentration of Ce in aboveground biomass was lower than root Ce content, and followed the dose-response trend. From values measured in natural soils around the world, our results continue to support the notion that REEs are of limited toxicity and not considered extremely hazardous to the environment. However, in areas where REE contamination is likely, the slow accumulation of these elements in the environment could become problematic. PMID:23978671

  1. Hydrothermal REE and Zr Ore Forming Processes in Peralkaline Granitic Systems

    NASA Astrophysics Data System (ADS)

    Gysi, A. P.

    2015-12-01

    Anorogenic peralkaline igneous systems display extreme enrichment of REE and Zr with a hydrothermal overprint leading to post-magmatic metal mobilization. Strange Lake in Canada, for example, is a mid-Proterozoic peralkaline granitic intrusion and host to a world-class REE-Zr deposit with >50 Mt ore (>1.5 wt.% REE and >3 wt.% Zr). In contrast to porphyry systems, peralkaline systems are poorly understood and hydrothermal metal mobilization models are only in the early stage of their development. This is partly due to the paucity of thermodynamic data for REE-bearing minerals and aqueous species, and the complexity of the hydrothermal fluids (enrichment of F, P and Cl), which make it difficult to develop thermodynamic models of metal partitioning. This study aims to show the link between alteration stages and metal mobilization using Strange Lake as a natural laboratory and combine these observations with numerical modeling. Four types of alteration were recognized at Strange Lake: i) alkali (i.e. K and Na) metasomatism related to interaction with NaCl-bearing orthomagmatic fluids, ii) acidic alteration by HCl-HF-bearing fluids originating from the pegmatites followed by iii) aegirinization of the border of the pegmatites and surrounding granites and by iv) pervasive Ca-F-metasomatism. The acidic alteration accounts for most of the hydrothermal metal mobilization in and outward from the pegmatites, whereas the Ca-F-metasomatism led to metal deposition and resulted from interaction of an acidic F-rich fluid with a Ca-bearing fluid. Numerical simulations of fluid-rock reactions with saline HCl-HF-bearing fluids at 400 °C to 250 °C indicate that temperature, availability of F/Cl and pH limit the mobility of Zr and REE. Fluids with pH <2 led to the formation of quartz and fluorite in the core of the pegmatites and to an increase in the stability of REE chloride species favorable for REE mobilization. The mobilization of Zr was favored at low temperature with the

  2. Use of arsenic and REE in black shales as potential environmental tracers in hydraulic fracturing operations

    NASA Astrophysics Data System (ADS)

    Yang, J.; Torres, M. E.; Haley, B. A.; McKay, J. L.; Algeo, T. J.; Hakala, A.; Joseph, C.; Edenborn, H. M.

    2013-12-01

    Black shales commonly targeted for shale gas development were deposited under low oxygen concentrations, and typically contain high As levels. The depositional environment governs its solid-phase association in the sediment, which in turn will influence degree of remobilization during hydraulic fracturing. Organic carbon (OC), trace element (TE) and REE distributions have been used as tracers for assessing deep water redox conditions at the time of deposition in the Midcontinent Sea of North America (Algeo and Heckel, 2008), during large-scale oceanic anoxic events (e.g., Bunte, 2009) and in modern OC-rich sediments underlying coastal upwelling areas (e.g., Brumsack, 2006). We will present REE and As data from a collection of six different locations in the continental US (Kansas, Iowa, Oklahoma, Kentucky, North Dakota and Pennsylvania), ranging in age from Devonian to Upper Pennsylvanian, and from a Cretaceous black shale drilled on the Demerara Rise during ODP Leg 207. We interpret our data in light of the depositional framework previously developed for these locations based on OC and TE patterns, to document the mechanisms leading to REE and As accumulation, and explore their potential use as environmental proxies and their diagenetic remobilization during burial, as part of our future goal to develop a predictive evaluation of arsenic release from shales and transport with flowback waters. Total REE abundance (ΣREE) ranged from 35 to 420 ppm in an organic rich sample from Stark shale, KS. PAAS-normalized REE concentrations ranged from 0.5 to 7, with the highest enrichments observed in the MREE (Sm to Ho). Neither the ΣREE nor the MREE enrichments correlated with OC concentrations or postulated depositional redox conditions, suggesting a principal association with aluminosilicates and selective REE fractionation during diagenesis. In the anoxic reducing environments in which black shales were deposited, sulfide minerals such as FeS2 trap aqueous arsenic in the

  3. Timescales and mechanisms of REE and Hf uptake in fossil bones

    NASA Astrophysics Data System (ADS)

    Herwartz, Daniel; Tütken, Thomas; Münker, Carsten; Jochum, Klaus Peter; Stoll, Brigitte; Sander, P. Martin

    2011-01-01

    Rare earth element (REE) patterns of fossil bones and teeth are widely used as proxies for provenance, taphonomy, and palaeoenvironment. In order to investigate if fossil bones behave as closed systems over geologic time, REE profiles were analysed by LA-ICPMS along cross sections of 54 bones from various well-characterised and well-dated settings. These include terrestrial and marine diagenetic environments, covering Early Triassic to Holocene ages. In general, all fossil bones exhibit the highest REE concentrations at the outer rim, gradually decreasing by up to four orders of magnitude toward the inner bone cortex. Intra-bone REE concentration gradients decrease significantly from Quaternary via Tertiary to Mesozoic specimens, suggesting long term REE uptake and open system behaviour of fossil bone. This view is further corroborated by 176Lu- 176Hf dating of selected samples, all yielding significantly younger ages than the known chronostratigraphic ages. Hence, there is clear evidence for long term open system behaviour of fossil bones with respect to REE, which is in marked contrast to currently accepted models suggesting that REE uptake is only early diagenetic. Although unexpected, statistically significant four to seven point isochrons are observed for four fossil dinosaur bone samples and one Upper Triassic Mastodonsaurus tooth with MSWDs ranging from 0.083 to 4.5. Notably, mobility of Lu alone cannot account for the observed age patterns. Assuming constant Lu uptake rates over time, the radiometric ages should only be as low as half of the chronostratigraphic age. However, a six-point isochron defined by subsamples of a single Upper Triassic Mastodonsaurus tooth yields an age of 65.2 ± 1.1 Ma (MSWD = 0.68), much younger than half of the stratigraphic age (ca. 234 Ma). Hence, Hf must also undergo late diagenetic exchange. Likely mechanisms to account for the presence of statistically meaningful isochrons as well as for the late diagenetic exchange of both

  4. REE Zonation in Garnet: new insights from combined Thermodynamic and Diffusion Modelling

    NASA Astrophysics Data System (ADS)

    Witte, C.; Konrad-Schmolke, M.

    2013-12-01

    Compositional variation in garnet provides an excellent record of element transport within their host rocks, as it precisely reflects the interplay between thermodynamically-controlled nutrient demand and kinetically-constrained element availability during growth. Element availability is controlled by (1) the thermodynamically controlled element distribution among co-existing phases and (2) by matrix transport properties. Our task is to distinguish between factors controlling the availability of major- and trace-elements and to quantify their diffusion length scales but this is hindered by the fact that the interplay of different rate-limiting factors on garnet growth and composition are not fully understood. These processes comprise: (1) fractional garnet crystallisation, which continuously changes the effective, i.e. reacting, bulk rock chemistry (EBC), which in turn influences garnet proportion, growth rate and composition; (2) kinetically-controlled element availability, such that grain boundary diffusion in the host rock's interconnecting transport matrix (ITM) or surface processes in reacting phases cannot keep pace with the material required for garnet nucleation and growth in homogeneous thermodynamic equilibrium with the coexisting phase assemblage and (3) reaction-controlled trace element availability in the host rock, which is often reflected in discontinuous trace element zoning patterns in garnet. A 1D diffusion and reaction model was developed to investigate REE distribution patterns in garnet. It combines PERPLEX thermodynamic forward modelling for a bulk rock composition along a P-T-path with control of diffusion rates in the matrix fluid which acts as a transport medium in the intergranular space. Initial REE distribution is controlled by standard distribution coefficients. Reactant phases are the source of REE and product minerals fractionate REE from the transport medium. Thus the uptake of REE in garnet is regulated by: (1) thermodynamically

  5. Mineral chemistry of Rare Earth Element (REE) mineralization, Browns Ranges, Western Australia

    NASA Astrophysics Data System (ADS)

    Cook, Nigel J.; Ciobanu, Cristiana L.; O'Rielly, Daniel; Wilson, Robin; Das, Kevin; Wade, Benjamin

    2013-07-01

    ‘Green energy futures’ are driving unprecedented demand for Rare Earth Elements (REE), underpinning significant exploration activity worldwide. Understanding how economic REE concentrations form is critical for development of exploration models. REE mineralisation in the Browns Ranges, Gordon Downs Region, Western Australia, comprises xenotime-dominant mineralisation hosted within Archaean to Palaeoproterozoic metasedimentary units (Browns Range Metamorphics). Mineralogical, petrographic and mineral-chemical investigation, including trace element analysis by Laser-Ablation Inductively-Coupled Plasma Mass Spectroscopy, gives insights into the mineralogical distribution and partitioning of REE, and also provides evidence for the genetic evolution of the Browns Range REE mineralisation via a succession of hydrothermal processes. Two main REE-bearing minerals are identified: xenotime [(Y,REE)PO4], which is HREE selective; and subordinate florencite [(REEAl3(PO4)2(OH)6] which is LREE selective. Two morphological generations of xenotime are recognised; compositions are however consistent. Xenotime contains Dy (up to 6.5 wt.%), Er (up to 4.35 wt.%), Gd (up to 7.56 wt.%), Yb (up to 4.65 wt.%) and Y (up to 43.3 wt.%). Laser Ablation ICP-MS element mapping revealed a subtle compositional zoning in some xenotime grains. LREE appear concentrated in the grain cores or closest to the initial point of growth whereas HREE, particularly Tm, Yb and Lu, are highest at the outer margins of the grains. The HREE enrichment at the outer margins is mimicked by As, Sc, V, Sr, U, Th and radiogenic Pb. Florencite is commonly zoned and contains Ce (up to 11.54 wt.%), Nd (up to 10.05 wt.%) and La (up to 5.40 wt.%) and is also notably enriched in Sr (up to 11.63 wt.%) and Ca. Zircon (which is not a significant contributor of REEs overall due to its low abundance in the rocks) is also enriched in REE (up to 13 wt.% ΣREE) and is the principal host of Sc (up to 0.8 wt.%). Early, coarse

  6. REE partitioning between apatite and melt in a peralkaline volcanic suite, Kenya Rift Valley

    USGS Publications Warehouse

    Macdonald, R.; Baginski, B.; Belkin, H.E.; Dzierzanowski, P.; Jezak, L.

    2009-01-01

    Electron microprobe analyses are presented for fluorapatite phenocrysts from a benmoreite-peralkaline rhyolite volcanic suite from the Kenya Rift Valley. The rocks have previously been well characterized petrographically and their crystallization conditions are reasonably well known. The REE contents in the M site increase towards the rhyolites, with a maximum britholite component of ~35 mol.%. Chondrite-normalized REE patterns are rather flat between La and Sm and then decrease towards Yb. Sodium and Fe occupy up to 1% and 4%, respectively, of the M site. The major coupled substitution is REE3+ + Si4+ ??? Ca2+ + P5+. The substitution REE3+ + Na+ ??? 2Ca2+ has been of minor importance. The relatively large Fe contents were perhaps facilitated by the low fo2 conditions of crystallization. Zoning is ubiquitous and resulted from both fractional crystallization and magma mixing. Apatites in some rhyolites are relatively Y-depleted, perhaps reflecting crystallization from melts which had precipitated zircon. Mineral/glass (melt) ratios for two rhyolites are unusually high, with maxima at Sm (762, 1123). ?? 2008 The Mineralogical Society.

  7. Optical spectra and luminescence of REE and TRU for analytical purposes in chloride melts

    SciTech Connect

    Aloy, A.S.; Gorshkov, N.G.; Nekhoroshkov, S.N.; Osipenko, A.G.; Mayorshin, A.A.

    2013-07-01

    This paper analyzes absorption spectra of molten salts containing some of the actinide and rare-earth elements (REE) and evaluated the prospects of using the individual transitions to control the composition of the spent molten salts using adsorption and luminescence spectroscopy from the standpoint of the theory of Judd-Ofelt. It is shown that the fluorescent method can be recommended only for the monitoring of the degree of purification of the molten salt from the REE in the final stage, when only trace amounts of fission products are in the molten salt. In this case, the content of REE in the molten process is much smaller than that of the used model samples and that eliminates the problem of a significant decrease in the population levels of fluorescent Eu{sup 3+} by quenching impurities. In addition, the presence of salt in the matrix of americium and curium can cause self-luminescence of Eu{sup 3+} due to alpha disintegration energy of transuranics, which also complicates the quantitative measurement of luminescence for the determination of REE.

  8. [Study on the Geochemical Anomalies Identification of REE Based on HJ-1A-HSI].

    PubMed

    Chen, Yong-gan; Wang, Mei-juan; Li, Peng

    2015-11-01

    The characteristic spectral bands of REE do not vary with the occurrence state, cannot be used to identify mineral species, but can prove the existence of its own. Here we report the spectrum characteristics of REE and their compounds by remote sensing wave band from visible light-near infrared, with the quantitative relationship between the contents of REE and absorption index of characteristic spectral bands. The experimental study was carried out in Bayan Obo area, Inner Mongolia. Spectrums and Nd contents of typical rock and ore samples were gathered and analyzed. There is positive correlation between the Nd content, the absorption depth and absorption index of different spectrum characteristics (correlation coefficient > 0.778). Moreover, the correlation between absorption index of 726-772 nm band and Nd content is the best, at 0. 937. As mentioned above, the quantitative model and the inversion information remote sensing geochemical anomaly of Nd were built by the band of HJ-1A-HIS hyperspectral remote sensing data. Our results consistent with 1:200,000 stream sediment geochemical anomalies of Nd. The model provides a new means for rapid extract regional geochemical anomalies of REE. PMID:26978930

  9. Major, trace and REE geochemistry of recent sediments from lower Catumbela River (Angola)

    NASA Astrophysics Data System (ADS)

    Vinha, Manuela; Silva, M. G.; Cabral Pinto, Marina M. S.; Carvalho, Paula Cristina S.

    2016-03-01

    The mineralogy, texture, major, trace and rare earth elements, from recent sediment samples collected in the lower Catumbela River, were analysed in this study to characterize and discuss the factors controlling its geochemistry and provide data that can be used as tracers of Catumbela River inputs to the Angolan continental shelf. The sediments are mainly sands and silty-sands, but sandy-silt also occurs and the mineralogy is composed of quartz, feldspar, phyllosilicates, magnetite, ilmenite and also carbonates when the river crosses limestones and marls in the downstream sector. The hydraulic sorting originates magnetite-ilmenite and REE-enriched minerals placers. The mineralogy of the sediments is controlled by the source rocks and the degree of chemical weathering is lower than erosion. The texture is mainly controlled by location. There is enrichment in all the analysed trace elements in the fine grained, clay minerals and Fe-oxy-hydroxides rich sediments, compared to the coarse grained and quartz plus feldspar rich ones. The coarse grained sediments (without the placers) are impoverished in ΣREE when compared with UCC and NASC compositions, while the fine grained sediments have ΣREE contents similar to UCC and NASC. The placers have ΣREE contents up to 959.59 mg/kg. The source composition is the dominant factor controlling the REE geochemistry of the analysed sediments as there is no difference in the (La/Yb)N, (La/Sm)N and (Gd/Yb)N ratios in coarse and fine grained sediments. The sorting of magnetite, ilmenite, zircon, throrite, thorianite, rutile and titanite explain the HREE/LREE enriched patterns of the coarse grained sediments.

  10. Neodymium isotopic study of rare earth element sources and mobility in hydrothermal Fe oxide (Fe-P-REE) systems

    SciTech Connect

    Gleason, J.D.; Marikos, M.A.; Barton, M.D.; Johnson, D.A.

    2000-03-01

    Rare earth element (REE)-enriched, igneous-related hydrothermal Fe-oxide hosted (Fe-P-REE) systems from four areas in North America have been analyzed for their neodymium iosotopic composition to constrain REE sources and mobility in these systems. The Nd isotopic results evidence a common pattern of REE concentration from igneous sources despite large differences in age (Proterozoic to Tertiary), tectonic setting (subduction vs. intraplate), and magmatic style (mafic vs. felsic). In the Middle Proterozoic St. Francois Mountains terrane of southeastern Missouri, {epsilon}{sub Nd} for Fe-P-REE (apatite, monazite, xenotime) deposits ranges from +3.5 to +5.1, similar to associated felsic to intermediate igneous rocks of the same age ({epsilon}{sub Nd} = +2.6 to +6.2). At the mid-Jurassic Humboldt mafic complex in western Nevada, {epsilon}{sub Nd} for Fe-P-REE (apatite) mineralization varies between +1.1 and +2.4, similar to associated mafic igneous rocks ({minus}1.0 to +3.5). In the nearby Cortez Mountains in central Nevada, mid-Jurassic felsic volcanic and plutonic rocks ({epsilon}{sub Nd} = {minus}2.0 to {minus}4.4) are associated with Fe-P-REE (apatite-monazite) mineralization having similar {epsilon}{sub Nd}({minus}1.7 to {minus}2.4). At Cerro de Mercado, Durango, Mexico, all assemblages analyzed in this Tertiary rhyolite-hosted Fe oxide deposit have identical isotopic compositions with {epsilon}{sub Nd} = {minus}2.5. These data are consistent with coeval igneous host rocks being the primary source of REE in all four regions, and are inconsistent with a significant contribution of REE from other sources. Interpretations of the origin of these hydrothermal systems and their concomitant REE mobility must account for nonspecialized igneous sources and varied tectonic settings.

  11. Neodymium isotopic study of rare earth element sources and mobility in hydrothermal Fe-oxide (Fe-P-REE) systems

    NASA Astrophysics Data System (ADS)

    Gleason, James D.; Marikos, Mark A.; Barton, Mark D.; Johnson, David A.

    2000-03-01

    Rare earth element (REE)-enriched, igneous-related hydrothermal Fe-oxide hosted (Fe-P-REE) systems from four areas in North America have been analyzed for their neodymium isotopic composition to constrain REE sources and mobility in these systems. The Nd isotopic results evidence a common pattern of REE concentration from igneous sources despite large differences in age (Proterozoic to Tertiary), tectonic setting (subduction vs. intraplate), and magmatic style (mafic vs. felsic). In the Middle Proterozoic St. Francois Mountains terrane of southeastern Missouri, ɛ Nd for Fe-P-REE (apatite, monazite, xenotime) deposits ranges from +3.5 to +5.1, similar to associated felsic to intermediate igneous rocks of the same age (ɛ Nd = +2.6 to +6.2). At the mid-Jurassic Humboldt mafic complex in western Nevada, ɛ Nd for Fe-P-REE (apatite) mineralization varies between +1.1 and +2.4, similar to associated mafic igneous rocks (-1.0 to +3.5). In the nearby Cortez Mountains in central Nevada, mid-Jurassic felsic volcanic and plutonic rocks (ɛ Nd = -2.0 to -4.4) are associated with Fe-P-REE (apatite-monazite) mineralization having similar ɛ Nd (-1.7 to -2.4). At Cerro de Mercado, Durango, Mexico, all assemblages analyzed in this Tertiary rhyolite-hosted Fe oxide deposit have identical isotopic compositions with ɛ Nd = -2.5. These data are consistent with coeval igneous host rocks being the primary source of REE in all four regions, and are inconsistent with a significant contribution of REE from other sources. Interpretations of the origin of these hydrothermal systems and their concomitant REE mobility must account for nonspecialized igneous sources and varied tectonic settings.

  12. Microbially mediated formation of a new REE enriched Mn-oxide, Ytterby mine, Sweden

    NASA Astrophysics Data System (ADS)

    Sjöberg, Susanne; Allard, Bert; Rattray, Jayne E.; Callac, Nolwenn; Skelton, Alasdair; Ivarsson, Magnus; Karlsson, Stefan; Sjöberg, Viktor; Dupraz, Christophe

    2016-04-01

    Characterization of a black substance seeping from fractured bedrock in a subterranean tunnel revealed a new, microbially mediated, secondary manganese oxide mineralisation, highly enriched in rare earth elements (REEs). This tunnel is dry and at shallow depth and was built to convert the former Ytterby mine, known for the discovery of yttrium (Y), scandium (Sc) and five rare earth elements, into a fuel deposit for the Swedish Armed Forces. As the type locality of these rare earth elements, the Ytterby mine gave its name to yttrium, ytterbium, erbium and terbium. Geochemical analysis shows that the substance is enriched in REEs with concentrations one to two orders of magnitude higher than the surrounding rocks. Elemental analysis and X-ray diffraction establish that the main component is a manganese oxide of the birnessite type (general formula: [Na,Ca]0.5[Mn(III),Mn(IV)]2O4xAq). There are also minor fractions of calcite, some other manganese oxides, feldspars, quartz and about 1% organic matter, but no iron oxides. Leaching studies (sequential and selective) were performed in order to establish how the minor components are associated with the matrix (in the lattice or merely adsorbed on the outer surface). It shows that the Ytterby birnessite contains about 1% REEs in the lattice, as well as calcium but no sodium. Formation of birnessite by manganese oxidizing bacteria is well-known (e.g. Tebo et al, 2004). Quantitative PCR shows that the total number of bacteria in the Ytterby substance is in the order 1010 cells per g substance while the water feeding the fracture has in the order of 106 cells per ml groundwater. qPCR data further confirm that manganese oxidizing microorganisms are present and that the abundance varies with the seasons. Analysis of the precipitated manganese using electron paramagnetic resonance spectroscopy shows that the substance is composed of two or more components, with one part having a biogenic signature. The occurrence of C31 to C35

  13. REE Mineralization in Kiruna-type Magnetite-Apatite Ore Deposits: Magmatism and Metasomatism

    NASA Astrophysics Data System (ADS)

    Harlov, D. E.

    2015-12-01

    Magnetite-apatite ore bodies of the Kiruna type occur worldwide and are generally associated with volcanic rocks or volcanism. They also show strong evidence of extensive metasomatism over a wide P-T range. Notable examples include the Kiirunavaara ore body, northern Sweden (Harlov et al., 2002, Chem. Geol., 191, 47-72); the Grängesberg ore body, central Sweden (Jonsson et al., 2010, NGF abstracts, vol 1, 88-89); the Mineville ore body, Adirondacks, New York, USA (McKeown and Klemc, 1956, U.S. Geol Sur Bull (1956), pp. 9-23); the Pea Ridge ore body, SE Missouri, USA (Kerr, 1998, MS Thesis, Univ. Windsor, Windsor, Ontario, Canada 113 pp); the Jurassic Marcona ore body in south-central Peru (Chen et al., 2010, Econ Geol, 105, 1441-1456); and a collection of ore bodies from the Bafq Region, central Iran (Daliran et al., 2010, Geol. Assoc. Canada, Short Course Notes, v. 20, p.147-159). In these ore bodies, low Th and U monazite, xenotime, allanite, REE carbonates, and/or REE fluorides are commonly associated with the apatite as inclusions, rim grains, or as independent grains in the surrounding mineral matrix. High contrast BSE imaging, coupled with EMPA and LA-ICPMS, indicates that the apatite has experienced fluid-induced alteration in the form of (Y+REE) + Na + Si + Cl depletion implying that it served as the source for the (Y+REE) (e.g. Kiirunavaara, northern Sweden; Harlov et al., 2002). Formation of monazite and xenotime associated with fluorapatite, as inclusions or rim grains, has experimentally been demonstrated to originate from the fluorapatite as the result of fluid-aided, coupled dissolution-reprecipitation processes (Harlov et al., 2005, Contrib. Mineral. Petrol. 150, 268-286). This is explains the low Th and U content of the monazite and xenotime. Fluid sources could range from 700-900 °C, residual, acidic (HCl, H2HSO4) grain boundary fluids, remaining after the last stages of ore body crystallization, to later stage, cooler (< 600 °C) (H2O-CO2-(Na

  14. Trace element and REE composition of five samples of the Yucca Mountain calcite-silica deposits. Special report No. 8

    SciTech Connect

    Livingston, D.

    1993-07-01

    The attached materials document the results of part of a recent effort of geochemical sampling and analysis at Yucca Mountain and nearby regions. The efforts come as a result of interest in comprehensive analyses of rare earth elements (REE), lanthanum (La) through lutecium (Lu). Several additional, non-REE analyses were obtained as well. Commercially available REE analyses have proved to be insufficiently sensitive for geochemical purposes. Dr. Roman Schmitt at the Radiation Center at Oregon State University in Corvallis was sent five samples as a trial effort. The results are very encouraging. The purpose of compiling Dr. Schmitt`s report and the other materials is to inform the sponsor of his independent observations of these results and other information that sent to him. To provide a more complete appreciation of the utility of REE analyses a copy of Dave Vaniman`s recent article is included in which he notes that REE analyses from Yucca Mountain indicate the occurrence of two distinctly different REE patterns as do several other chemical parameters of the calcite-silica deposits. Our four samples with high equivalent CaCO{sub 3} were collected from sites we believe to be spring deposits. One sample, 24D, is from southern Crater Flat which is acknowledged by U.S.G.S. investigators to be a spring deposit. All four of these samples have REE patterns similar to those from the saturated zone reported by Vaniman.

  15. Geochemical constraints on the genesis of the Bayan Obo Fe Nb REE deposit in Inner Mongolia, China

    NASA Astrophysics Data System (ADS)

    Yang, Xiao-Yong; Sun, Wei-Dong; Zhang, Yu-Xu; Zheng, Yong-Fei

    2009-03-01

    Trace element and isotopic compositions of carbonate from ore bodies, country rock which hosts the ore bodies (H8 dolomite), a carbonatite dyke exposed in Dulahala near Bayan Obo, and rare earth element (REE)-rich dolomite in Bayan Obo have been determined to understand the genesis of the Bayan Obo Fe-Nb-REE ore deposit, the world's largest resource of REE. The REE and trace element distribution patterns of samples from the REE-rich carbonatite dykes are identical to those of mineralized carbonate rocks, indicating a genetic linkage between the REE-rich carbonatite and mineralization in this region. By contrast, carbon and oxygen isotopes in the mineralized carbonate varied significantly, δ 13C = -7.98‰ to -1.12‰, δ 18O = 8.60-25.69‰, which are distinctively different from those in mantle-derived carbonatite. Abnormal isotopic fractionations between dolomite and calcite suggest that these two minerals are in disequilibrium in the carbonatite dyke, ore bodies, and H8 marble from Bayan Obo. This isotopic characteristic is also found in mineralized sedimentary marine micrite from Heinaobao, ˜25 km southeast of the Bayan Obo Fe-Nb-REE ore deposit. These facts imply that the carbonate minerals in the Bayan Obo deposit have resulted from sedimentary carbonate rocks being metasomatised by mantle-derived fluids, likely derived from a REE-enriched carbonatitic magma. The initial Nd isotope values of ore bodies and carbonatite dykes are identical, indicating that ore bodies, carbonatite dykes and veins may have a similar REE source.

  16. Uptake and Effects of Six Rare Earth Elements (REEs) on Selected Native and Crop Species Growing in Contaminated Soils

    PubMed Central

    Carpenter, David; Boutin, Céline; Allison, Jane E.; Parsons, Jessica L.; Ellis, Deanna M.

    2015-01-01

    Rare earth elements (REEs) have become increasingly important metals used in modern technology. Processes including mining, oil refining, discarding of obsolete equipment containing REEs, and the use of REE-containing phosphate fertilizers may increase the likelihood of environmental contamination. However, there is a scarcity of information on the toxicity and accumulation of these metals to terrestrial primary producers in contaminated soils. The objective of this work was to assess the phytotoxicity and uptake from contaminated soil of six REEs (chloride forms of praseodymium, neodymium, samarium, terbium, dysprosium, and erbium) on three native plants (Asclepias syriaca L., Desmodium canadense (L.) DC., Panicum virgatum L.) and two crop species (Raphanus sativus L., Solanum lycopersicum L.) in separate dose-response experiments under growth chamber conditions. Limited effects of REEs were found on seed germination and speed of germination. Effects on aboveground and belowground biomass were more pronounced, especially for the three native species, which were always more sensitive than the crop species tested. Inhibition concentrations (IC25 and IC50) causing 25 or 50% reductions in plant biomass respectively, were measured. For the native species, the majority of aboveground biomass IC25s (11 out of 18) fell within 100 to 300 mg REE/kg dry soil. In comparison to the native species, IC25s for the crops were always greater than 400 mg REE/kg, with the majority of results (seven out of 12) falling above 700 mg REE/kg. IC50s were often not detected for the crops. Root biomass of native species was also affected at lower doses than in crops. REE uptake by plants was higher in the belowground parts than in the above-ground plant tissues. Results also revealed that chloride may have contributed to the sensitivity of the native species, Desmodium canadense, one of the most sensitive species studied. Nevertheless, these results demonstrated that phytotoxicity may be a

  17. Geological and geochemical characteristics in the paleo-weathering crust sedimentary type REE deposits, western Guizhou, China

    NASA Astrophysics Data System (ADS)

    Zhou, Lingjie; Zhang, Zhengwei; Li, Yujiao; You, Fuhua; Wu, Chengquan; Zheng, Chaofei

    2013-09-01

    A supergene REE deposit closely interrelated with the weathering of the Emeishan basalt formation was produced in the Xuanwei formation, the overlying stratum of the late Permian Emeishan basalt formation in West Guizhou, China. The host strata consist primarily of offwhite kaolinite clay rock and/or grayish black carbonaceous shale. Mineralogical analyses reveal that kaolinites are the major minerals in REE ores with small amounts of smectite, illite, boehmite, hornblende, pyrophyllite, calcite, dolomite and/or iron-bearing minerals, with a certain proportion of feldspar, quartz crystal debris and noncrystal debris. Geochemical analyses reveal high enrichment of trace elements like Cu, Nb, Ta, Zr and Hf. The host strata feature considerable lithological variability, close interrelation of the REE grade with the lithology and uneven spatial distribution of the REE ores, which are mostly found in Lufang, Maojiaping and Zhangsigou profiles of Weining County and can be as thick as 20 m. Of the five stratigraphic profiles, 48% have their whole-rock ∑REE higher than 1000 ppm. The REE in this framework consists primarily of ion adsorbed phases and REE-rich residual independent mineral phases. Comprehensive analyses suggest that the source may not only include the Emeishan basalt, but the intermediate acid volcanic rocks evolved from the Emeishan basalt in the later periods; the hydrothermal alteration subsequently imposed on the host strata might have boosted the mineralization of the rare earth. The preliminary genetic model should have been: the denudation product from the weathering of the parent rock was migrated to the sea-continental margin at the continent side carrying huge quantities of REE with it and was preserved by the quick marine transgression. The host strata consist primarily of kaolinite clay rock and/or carbonaceous shale, which are so far believed to be a sedimentary type REE deposit closely interrelated with weathering effect.

  18. Uptake and Effects of Six Rare Earth Elements (REEs) on Selected Native and Crop Species Growing in Contaminated Soils.

    PubMed

    Carpenter, David; Boutin, Céline; Allison, Jane E; Parsons, Jessica L; Ellis, Deanna M

    2015-01-01

    Rare earth elements (REEs) have become increasingly important metals used in modern technology. Processes including mining, oil refining, discarding of obsolete equipment containing REEs, and the use of REE-containing phosphate fertilizers may increase the likelihood of environmental contamination. However, there is a scarcity of information on the toxicity and accumulation of these metals to terrestrial primary producers in contaminated soils. The objective of this work was to assess the phytotoxicity and uptake from contaminated soil of six REEs (chloride forms of praseodymium, neodymium, samarium, terbium, dysprosium, and erbium) on three native plants (Asclepias syriaca L., Desmodium canadense (L.) DC., Panicum virgatum L.) and two crop species (Raphanus sativus L., Solanum lycopersicum L.) in separate dose-response experiments under growth chamber conditions. Limited effects of REEs were found on seed germination and speed of germination. Effects on aboveground and belowground biomass were more pronounced, especially for the three native species, which were always more sensitive than the crop species tested. Inhibition concentrations (IC25 and IC50) causing 25 or 50% reductions in plant biomass respectively, were measured. For the native species, the majority of aboveground biomass IC25s (11 out of 18) fell within 100 to 300 mg REE/kg dry soil. In comparison to the native species, IC25s for the crops were always greater than 400 mg REE/kg, with the majority of results (seven out of 12) falling above 700 mg REE/kg. IC50s were often not detected for the crops. Root biomass of native species was also affected at lower doses than in crops. REE uptake by plants was higher in the belowground parts than in the above-ground plant tissues. Results also revealed that chloride may have contributed to the sensitivity of the native species, Desmodium canadense, one of the most sensitive species studied. Nevertheless, these results demonstrated that phytotoxicity may be a

  19. Cause of large negative Eu anomaly in the highly evolved A-type granites with REE tetrad pattern

    NASA Astrophysics Data System (ADS)

    Lee, S.; Asahara, Y.; Tanaka, T.; Lee, M.; Lee, S. R.

    2013-12-01

    REE tetrad pattern with strongly large negative Eu anomaly is one of the specific geochemical phenomena observed in the highly evolved, fractionated granite or A-type granite. The large negative Eu anomaly from the highly evolved or fractionated granites related with REE tetrad effect was discussed in a lot of literatures (e.g. [1] Muecke and Clarke, 1981; [2] Irber, 1999; [3] Jahn et al., 2001). Recently, Lee et al.[4] also suggested that Eu anomalies and REE tetrad pattern from the highly fractionated A-type Muamsa and Weolaksan granites in the Okcheon Metamorphic Belt, Korea, might be associated with a fractionation between the residual melt and a coexisting aqueous high temperature fluid. Their origin and geochemical significance are ongoing yet. In order to clarify cause of large negative Eu anomaly in the granite with REE tetrad effect more clearly, we reanalyzed REE abundance of the Muamsa and Weolaksan granites using MC-ICP-MS at the origins laboratory of the University of Chicago. We also measured REE abundances of the constituent minerals using quadruple ICP-MS at the Korea Polar Research Institute. In this report, we show the re-analyzed REE data from the whole rock as well as new REE data from constituent minerals of the granite with REE tetrad effect. Then, we discuss the cause of large negative Eu anomaly in the highly evolved granite with REE tetrad effect. Especially, the granites with very large negative Eu anomaly also show large negative Ce anomaly. Lee et al. [4] mentioned that negative Ce anomalies were formed after granite emplacement. However, our new data indicate that negative Ce anomaly might be formed during the same geochemical process with very large negative Eu anomaly. This suggests that the REE tetrad effect may be related with a change of oxidation state during a magma evolution. Therefore, we will discuss REE tetrad effect, negative Eu and Ce anomaly as an indicator for the change of oxidation state of magma during the emplacement

  20. Partition coefficients of Hf, Zr, and REE between zircon, apatite, and liquid

    USGS Publications Warehouse

    Fujimaki, H.

    1986-01-01

    Concentration ratios of Hf, Zr, and REE between zircon, apatite, and liquid were determined for three igneous compositions: two andesites and a diorite. The concentration ratios of these elements between zircon and corresponding liquid can approximate the partition coefficient. Although the concentration ratios between apatite and andesite groundmass can be considered as partition coefficients, those for the apatite in the diorite may deviate from the partition coefficients. The HREE partition coefficients between zircon and liquid are very large (100 for Er to 500 for Lu), and the Hf partition coefficient is even larger. The REE partition coefficients between apatite and liquid are convex upward, and large (D=10-100), whereas the Hf and Zr partition coefficients are less than 1. The large differences between partition coefficients of Lu and Hf for zircon-liquid and for apatite-liquid are confirmed. These partition coefficients are useful for petrogenetic models involving zircon and apatite. ?? 1986 Springer-Verlag.

  1. DEMNUni: ISW, Rees-Sciama, and weak-lensing in the presence of massive neutrinos

    NASA Astrophysics Data System (ADS)

    Carbone, Carmelita; Petkova, Margarita; Dolag, Klaus

    2016-07-01

    We present, for the first time in the literature, a full reconstruction of the total (linear and non-linear) ISW/Rees-Sciama effect in the presence of massive neutrinos, together with its cross-correlations with CMB-lensing and weak-lensing signals. The present analyses make use of all-sky maps extracted via ray-tracing across the gravitational potential distribution provided by the ``Dark Energy and Massive Neutrino Universe'' (DEMNUni) project, a set of large-volume, high-resolution cosmological N-body simulations, where neutrinos are treated as separate collisionless particles. We correctly recover, at 1–2% accuracy, the linear predictions from CAMB. Concerning the CMB-lensing and weak-lensing signals, we also recover, with similar accuracy, the signal predicted by Boltzmann codes, once non-linear neutrino corrections to HALOFIT are accounted for. Interestingly, in the ISW/Rees-Sciama signal, and its cross correlation with lensing, we find an excess of power with respect to the massless case, due to free streaming neutrinos, roughly at the transition scale between the linear and non-linear regimes. The excess is ~ 5 – 10% at l ~ 100 for the ISW/Rees-Sciama auto power spectrum, depending on the total neutrino mass Mν, and becomes a factor of ~ 4 for Mν = 0.3 eV, at l ~ 600, for the ISW/Rees-Sciama cross power with CMB-lensing. This effect should be taken into account for the correct estimation of the CMB temperature bispectrum in the presence of massive neutrinos.

  2. The role of natural solidification paths on REE partitioning between clinopyroxene and melt

    NASA Astrophysics Data System (ADS)

    Scarlato, P.; Mollo, S.; Blundy, J. D.; Iezzi, G.; Tiepolo, M.

    2014-03-01

    We document for the first time the role played by natural solidification paths on the partitioning of rare earth elements (REE) between clinopyroxene and melt. To do this, we investigated the compositional variation of clinopyroxenes formed under increasing cooling rate conditions from core to rim of a dike at Mt. Etna volcano. As the rate of cooling increases, clinopyroxenes are progressively depleted in Si + Ca + Mg counter-balanced by enrichments in Al + Na + Ti. Consequently, the concentration of REE in clinopyroxene increases due to an increased ease of locally balancing the excess charge at the M2 site as the number of surrounding tetrahedral aluminium atoms increases. Since Aliv in clinopyroxene is a charge-balancing cation for REE, the partition coefficients (DREE) measured at the dike chilled margin are distinctly higher than those from the dike interior. We conclude that, in naturally solidifying magmas, kinetically controlled cation substitution reactions can be treated in terms of the energetics of the various charge-imbalanced configurations. This finding is corroborated by the near-parabolic dependence of DREE on cation radius due to charge-balance mechanisms described by the lattice strain model.

  3. Rearrangement of REE's in Austin Glen Fm. (Ord. ), Ulster Co. , NY

    SciTech Connect

    Bock, B.; McLennan, S.M.; Hanson, G.N. . Dept. of ESS)

    1993-03-01

    Austin Glen turbidites are part of the allochthonous Taconic sequence of the Appalachian foreland basin. Graywackes in the sequence are rich in quartz, sedimentary rock fragments and carbonate, but have little feldspar. The abundant matrix makes it difficult to recognize volcanic components. REE patterns and Nd isotopes were analyzed to distinguish the relative abundance of volcanic versus older crustal components. REE patterns for shales and graywackes in a hundred-meter section are characterized by variable LREE-enrichment. An inclined array was expected on the f[sub Sm/Md] [minus] [var epsilon][sub Nd] diagram resulting from mixed sources. The vertical array shows that the samples had the same Nd-isotopic composition at 470 Ma. The restricted [var epsilon][sub Nd] of 8.0 [plus minus] 0.4 indicates the provenance was dominated by older crustal components that likely had similar Sm/Nd. The large variation in f[sub Sm/Nd] requires rearrangement of the REEs during sedimentary processes or early diagenesis at about 470 Ma.

  4. Evidence for pressure dependence of the peak position in the REE mineral/melt partition patterns of clinopyroxene

    SciTech Connect

    Liu, C.Q. Univ. of Tokyo ); Masuda, A.; Shimizu, H. ); Xie, G.H. )

    1992-04-01

    Major element compositions, REE abundances, and strontium and neodymium isotope ratios were measured for three megacrysts of garnet, five of clinopyroxene, one of amphibole and the host alkali basalts from two volcanoes in northeastern China. Strontium and neodymium isotopic data and major elements (Fe and Mg) indicate a cognate origin of megacrysts and host lavas. Logarithmic values of REE partition coefficients for these minerals were found to vary parabolically with ionic radius, and hence the REEs in these three minerals are considered to substitute primarily into only one lattice site of each mineral. The ionic radius (optimum radius) defined by the position of peak top of the parabola is variable. Based on the REE partition coefficient data for both experimental and naturally existing clinopyroxene/melt pairs, the change of the optimum radius may be interpreted to be mainly pressure dependent.

  5. Parameterized Lattice Strain Models for REE Partitioning between Amphibole and Silicate Melt

    NASA Astrophysics Data System (ADS)

    Shimizu, K.; Liang, Y.; Sun, C.; Jackson, C.; Saal, A. E.

    2015-12-01

    The distribution of REE between amphibole and silicate melt is important for understanding a variety of igneous processes involving amphibole. In general, amphibole-melt REE partition coefficients (DREE) depend on pressure (P), temperature (T), and compositions of amphibole and melt. A previous study parameterized the DREE in amphibole-melt solely as a function of melt composition [1]. Here, we use published REE partitioning data between amphibole and basaltic melt, the lattice strain model [2], and non-linear least squares regression method to parameterize key partitioning parameters in the lattice strain model (D0, r0, and E) as a function of P, T, and both amphibole and melt compositions. We focus on experimental data obtained by LA-ICP-MS and ion probe, and experiments close to equilibrium. Amphiboles and coexisting melts from the 38 experiments that we compiled span a wide range of compositions with the Mg# of amphibole and melt ranging from 36 to 100 and 15 to 99, respectively. Two models, which give nearly identical results, are explored in this study. In the first model, D0 is a function of T and amphibole composition: it negatively correlates with T and MgM1,2,3 content in amphibole, and positively correlates with TiM1,2,3 content in amphibole. In the second model, D0 is solely a function of the melt composition: it negatively correlates with the mole fraction of Ca in the melt. Interestingly, r0 and E are both constant and identical between the two models, suggesting D0 in the two models are equivalent. The latter allows us to develop a new thermometer for amphibole-melt equilibria. As an independent test, we compared model-derived temperatures with those reported in the phase equilibrium experiments. The predicted temperatures are within ±41°C on average of the reported temperatures, adding confidence to our parameterizations of D0. Our two parameterized lattice strain models can be used to model REE fractionation between amphibole and basaltic melts

  6. Sorption of REE and TPE from HNO{sub 3} solutions on strong-acid sulfonated cation exchanger KU-2

    SciTech Connect

    Chuveleva, E.A.; Kharitonov, O.V.; Firsova, L.A.

    1995-05-01

    Sorption of rare earths (REE) on the strong-acid sulfonated cation exchanger KU-2 is studied as a function of the solution acidity (0.1-2.0 M HNO{sub 3}) and REE concentration. In concentrated nitrate solutions where M(NO{sub 3}){sub 2}{sup +} and M(NO{sub 3}){sub 2}{sup +} can form and be sorbed by the cation exchanger, the capacity of the exchanger seems to increase by 20%.

  7. REE-bearing minerals in a Ti-rich vein from the Adamello contact aureole (Italy)

    NASA Astrophysics Data System (ADS)

    Gieré, Reto; Williams, C. Terry

    1992-10-01

    Zirconolite, aeschynite-(Ce), titanite and apatite have been found as minor or accessory minerals in a Ti-rich (TiO2=2.1 4.5 wt.%) hydrothermal vein occurring in dolomite marbles at the contact with a tonalite intrusion of the Tertiary Adamello batholith (northern Italy). The vein consists of four distinct mineral zones, comprising from margin to center: (1) forsterite+calcite, (2) pargasite+calcite+titanite+sulfides, (3) phlogopite +calcite+titanite+sulfides, and (4) titanian clinohumite +spinel+calcite+sulfides. Zirconolite occurs in two vein zones only: in the phlogopite zone it is invariably anhedral, often corroded, and exhibits complex chemical zonation patterns. In the titanian clinohumite zone zirconolite is idiomorphic and characterized by a pronounced discontinous chemical zoning, but shows no evidence of corrosion. The considerable compositional variation observed for zirconolite (in wt.%: ∑(REE2O3)=0.74 16.8, UO2=0.59 24.0, ThO2=0.67 17.1) is due to the zoning, and may be attributed to four major substitutions described by the exchange vectors: 1. (Th, U) (Mg, Fe2+) Ca-1 Ti-1 2. REE Al Ca-1 Ti-1 3. REE Fe2+ (Nb, Ta) Ca-1 Ti-1 4. Hf Zr-1 Exchange vector (2) is effective at total REE2O3 contents up to approximately 5 wt.%, whereas vector (3) is operating at higher concentrations. Both titanite and aeschynite-(Ce) exhibit, like zirconolite, complex chemical zonation patterns which document that the trace element content of the metasomatic fluid was variable during the vein-forming process. As indicated by thermodynamic analysis of the phase assemblages, the vein zones containing the REE-bearing minerals formed at 500 600°C (Ptotal≈2 kbar) from a reducing fluid rich in H2S, HCl°, HF° and phosphorus, but relatively poor in CO2(XCO 2 ≈0.2). Geochemical and isotopic data are consistent with the interpretation of the fluid as being derived from the nearby tonalite intrusion. The abundance of idiomorphic fluor-apatite as well as textural relations

  8. Temperatures and cooling rates recorded in REE in coexisting pyroxenes in ophiolitic and abyssal peridotites

    NASA Astrophysics Data System (ADS)

    Dygert, Nick; Liang, Yan

    2015-06-01

    Mantle peridotites from ophiolites are commonly interpreted as having mid-ocean ridge (MOR) or supra-subduction zone (SSZ) affinity. Recently, an REE-in-two-pyroxene thermometer was developed (Liang et al., 2013) that has higher closure temperatures (designated as TREE) than major element based two-pyroxene thermometers for mafic and ultramafic rocks that experienced cooling. The REE-in-two-pyroxene thermometer has the potential to extract meaningful cooling rates from ophiolitic peridotites and thus shed new light on the thermal history of the different tectonic regimes. We calculated TREE for available literature data from abyssal peridotites, subcontinental (SC) peridotites, and ophiolites around the world (Alps, Coast Range, Corsica, New Caledonia, Oman, Othris, Puerto Rico, Russia, and Turkey), and augmented the data with new measurements for peridotites from the Trinity and Josephine ophiolites and the Mariana trench. TREE are compared to major element based thermometers, including the two-pyroxene thermometer of Brey and Köhler (1990) (TBKN). Samples with SC affinity have TREE and TBKN in good agreement. Samples with MOR and SSZ affinity have near-solidus TREE but TBKN hundreds of degrees lower. Closure temperatures for REE and Fe-Mg in pyroxenes were calculated to compare cooling rates among abyssal peridotites, MOR ophiolites, and SSZ ophiolites. Abyssal peridotites appear to cool more rapidly than peridotites from most ophiolites. On average, SSZ ophiolites have lower closure temperatures than abyssal peridotites and many ophiolites with MOR affinity. We propose that these lower temperatures can be attributed to the residence time in the cooling oceanic lithosphere prior to obduction. MOR ophiolites define a continuum spanning cooling rates from SSZ ophiolites to abyssal peridotites. Consistent high closure temperatures for abyssal peridotites and the Oman and Corsica ophiolites suggests hydrothermal circulation and/or rapid cooling events (e.g., normal

  9. Florencite-(La) with fissiogenic REEs from a natural fission reactor at Bangombe, Gabon

    SciTech Connect

    Janeczek, J.; Ewing, R.C.

    1996-09-01

    Florecite-(La) (La/Ce = 1.09) with fissiogenic REEs and florecite-(Ce) (La/Ce = 0.62) have been identified in illite from the clay mantle surrounding a natural, 2 Ga fission reactor at Bangombre and in sandstone beneath the reactor zone, respectively. Florencite-(Ce) is apparently unrelated to nuclear processes and occurs with monazite-(Ce), apatite, TiO{sub 2} (probably anatase), zircon, and illite. Grains of florencite-(Ce) contain inclusions of thorite, chalcopyrite, and galena. Florencite-(La) was found 5 cm from the {open_quotes}core{close_quotes} of the reactor and contains inclusions of galena and U-Ti-bearing phases. Secondary uraninite and coffinite have precipitated on some of the florencite grains. The chemical composition of florencite-(La) as determined by electron microprobe analysis is (La{sub 0.38}Ce{sub 0.35}Nd{sub 0.06}Sm{sub 0.01}-Ca{sub 0.03}Sr{sub 0.17})(Al{sub 2.98}Fe{sub 0.02}{sup 3+})(PO{sub 4})[PO{sub 3.80}(OH){sub 0.20}](OH){sub 6}. Secondary ion mass spectrometry revealed that between 27 and 30% of Nd and 67 and 71% of Sm in florencite-(La) is fissiogenic. The presence of fissiogenic REEs in {open_quotes}florencite{close_quotes} from the reactor zone in Bangombe and their preferential concentration in florencite relative to the bulk sample of clay demonstrate that aluminous phosphates may have played a more significant role in the fixation of fissiogenic REES released from uraninite after the sustained fission reactions than sorption onto clays. 30 refs., 3 figs., 2 tabs.

  10. REE, trace elements, Sr, Pb, C, and O isotopes in a zoned skarn ore deposit

    SciTech Connect

    Langmuir, C.; LeHuray, A.; Fairbanks, R.; Meinert, L.

    1985-01-01

    The Groundhog skarn in the Central Mining District, New Mexico, is zoned along its >2km length adjacent to a dike swarm which trends NE toward the Santa Rita porphyry Cu deposit. Isotopes and trace elements in whole rocks and mineral separates from skarn and adjacent carbonate allow the study of the source of the metals and the systematics of trace element behavior in a skarn system. (1) /sup 87/Sr//sup 86/Sr ratios are uniform (.7083 +/- 1) in the carbonate host, but they range up to .714 in hydrothermal calcite and pyx from the skarn, values distinct from both Santa Rita (.706) and carbonate. (2) delta/sup 18/O (SMOW) in carbonate ranges from (+6.3 -+ 23) and is correlated positively with delta/sup 13/C (-5.6-+2.4) and negatively with /sup 87/Sr//sup 86/Sr. Several trace elements also correlate with delta/sup 18/O. (3) Pb isotopes in galenas lie on the regression line for southwestern New Mexico Proterozoic crust. PbS from the skarn closest to Santa Rita has isotope ratios identical to PbS from the Santa Rita pit. (4) Most of the REE are not in gar or pyx. REE abundances are <1X chondrites after HC1 leaches, but in unleached samples can be >20X chondrites. All pyx separates have deep negative Ce and very deep Eu anomalies. Sr isotopes show that neither Santa Rita magma nor carbonate is the sole source of Sr. Pb isotopes are consistent with a Santa Rita source. The Ce anomaly suggests a seawater source for the REE. The data show that many of the metals in the skarn are not derived from the Santa Rita porphyry, and suggest that different elements may be derived from different source rocks.

  11. Inter- and intra-crystal REE variations in apatite from the Bob Ingersoll pegmatite, Black Hills, South Dakota

    SciTech Connect

    Jolliff, B.L.; Papike, J.J.; Shearer, C.K. ); Shimizu, N. )

    1989-02-01

    Concentrations of rare earth elements (REE) have been measured on a suite of apatite crystals from an internally zoned granitic pegmatite enriched in Li, B, Be, F, Nb, Ta, Sn and U with a Cameca IMS 3f ion microprobe using energy filtering. An apatite specimen from the Tin Mountain pegmatite, analyzed previously by isotope dilution, was used as a standard. The chondrite-normalized pattern determined with the ion microprobe closely matches the pattern determined by isotope dilution, with maxima at Sm and Dy, and minima at Nd and Er. Apatite samples from the Bob Ingersoll pegmatite show a large range of REE patterns and concentrations. In one case, apatite crystals within millimeters show differences in REE concentrations and pattern shapes, including a switch from positive to negative Eu anomalies. These effects may be coupled with non-ideal partitioning of REE in a heterogeneous mixture of melt, aqueous fluid and crystals. REE concentrations in apatite samples from the different pegmatite zones indicate a large variation in outer zones, high concentrations near the pegmatite core, and very low concentration in the core. Patterns are flat to slightly inclined (Ce/Yb: 1 to 5), and most samples have positive Eu anomalies. The magnitude of positive Eu anomalies decreases with inward position in the pegmatite, possibly indicating a progressive increase in {line integral}O{sub 2}, and a sharp increase may be indicated by systematic Ce depletion in apatite from the pegmatite core. REE-specific volatile complexes may contribute to variations, including unusual kinks, observed in REE patterns of apatite from mineral assemblages in upper parts of the pegmatite.

  12. The effect of particulate dissolution on the neodymium (Nd) isotope and Rare Earth Element (REE) composition of seawater

    NASA Astrophysics Data System (ADS)

    Pearce, Christopher R.; Jones, Morgan T.; Oelkers, Eric H.; Pradoux, Catherine; Jeandel, Catherine

    2013-05-01

    The exchange of material between particulates and seawater along the continental margins, a process commonly referred to as boundary exchange, is thought to play a significant role in controlling the neodymium (Nd) isotope and Rare Earth Element (REE) composition of the oceans. This study provides experimental verification of this concept by quantifying the effect of particulate dissolution in seawater on dissolved ɛNd and REE compositions. Three closed-system experiments were performed using basaltic particulate material of riverine, estuarine and marine origin. The release of Nd from this basaltic material increased the ɛNd composition of seawater in all three experiments, with a ɛNd value close to that of the associated sediment being achieved within 80 days in all experiments. Mass balance indicates that up to 0.4% of Nd from the particulate phase was released to the seawater over the duration of these experiments, and that the rate of release varied according to particulate origin and surface area. Progressive variations in the PAAS normalised REE patterns, as well as the Eu and Ce anomalies and La/Yb ratio, demonstrate that REEs were also transferred from the basaltic particulates to seawater during the experiments. Despite evidence for the release of REEs from the particulate material, dissolved REE abundances decreased during the experiments, and are thought to reflect incorporation into the REE-phosphate mineral rhabdophane. Together these experimental results confirm that elemental release from basaltic sediments on the ocean margins is a significant marine flux that can have a major control on the composition of seawater.

  13. Sm-Nd isotopic systematics and REE abundance studies of the ALH-765 eucrite

    NASA Technical Reports Server (NTRS)

    Nakamura, N.; Tatsumoto, M.; Coffrant, D.

    1983-01-01

    Analyses of Sm-Nd systematics and REE concentrations were carried out for the whole rock and mineral separates from the ALH-765 meteorite. A Sm-Nd age of 4.52 + or - 0.09 (2 sigma) b.y. and an initial Nd-143/Nd-144 ratio of 0.50675 + or 0.00011 (2 sigma) have been obtained. The previously reported Ce irregularities have been re-examined in this work. The large Ce anomalies and some minor Sm-Nd system disturbances observed for the meteorite may be interpreted as results of terrestrial weathering effects.

  14. Behaviour of REEs in a tropical estuary and adjacent continental shelf of southwest coast of India: Evidence from anomalies

    NASA Astrophysics Data System (ADS)

    Deepulal, P. M.; Kumar, T. R. Gireesh; Sujatha, C. H.

    2012-10-01

    The distribution and accumulation of the rare earth elements (REE) in the sediments of the Cochin Estuary and adjacent continental shelf were investigated. The rare earth elements like La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu and the heavy metals like Mg, V, Cr, Mn, Fe, Cu, Zn, U, Th were analysed by using standard analytical methods. The Post-Archean Australian Shale composition was used to normalise the rare earth elements. It was found that the sediments were more enriched with the lighter rare earth elements than the heavier ones. The positive correlation between the concentrations of REE, Fe and Mn could explain the precipitation of oxyhydroxides in the study area. The factor analysis and correlation analysis suggest common sources of origin for the REEs. From the Ce-anomalies calculated, it was found that an oxic environment predominates in all stations except the station No. 2. The Eu-anomaly gave an idea that the origin of REEs may be from the feldspar. The parameters like total organic carbon, U/Th ratio, authigenic U, Cu/Zn, V/Cr ratios revealed the oxic environment and thus the depositional behaviour of REEs in the region.

  15. Hf, Zr, and REE partition coefficients between ilmenite and liquid - Implications for lunar petrogenesis

    NASA Technical Reports Server (NTRS)

    Nakamura, Y.; Fujimaki, H.; Nakamura, N.; Tatsumoto, M.; Mckay, G. A.

    1986-01-01

    Partition coefficients (D) between ilmenite and coexisting liquid were determined under near-lunar conditions for Hf, Zr, and REE. Through isotope dilution analysis, ilmenite D values of 0.41 and 0.33 were obtained for Hf and Zr respectively, values significantly lower than those of ilmenite from a kimberlite megacryst. Partition coefficients of REE for the synthesized ilmenite are slightly smaller than those of ilmenite from the kimberlite megacryst, and the lunar (Lu) partition coefficient is 0.056. These results suggest that ilmenite was significant in the lunar-Hf evolution of lunar mare basalts. Using lunar and Hf D values for ilmenite, the Lu-Hf evolution of lunar cumulates and the coexisting magma was examined for various crystallization sequences. The Lu-Hf variation trend of most high-Ti mare basalts is explained by a small degree of partial cumulate melting, though a higher degree is required to explain the variation of very low-Ti basalts, green glass, and Apollo 12 low-Ti basalts. Apollo 15 low-Ti basalts may require chromite crystallization as well.

  16. Non-Gaussianity and the CMB bispectrum: Confusion between primordial and lensing-Rees-Sciama contribution?

    SciTech Connect

    Mangilli, Anna; Verde, Licia

    2009-12-15

    We revisit the predictions for the expected cosmic microwave background bispectrum signal from the cross-correlation of the primary-lensing-Rees-Sciama signal; we point out that it can be a significant contaminant to the bispectrum signal from primordial non-Gaussianity of the local type. This non-Gaussianity, usually parametrized by the non-Gaussian parameter f{sub NL}, arises, for example, in multifield inflation. In particular both signals are frequency-independent, and are maximized for nearly squeezed configurations. While their detailed scale-dependence and harmonic imprints are different for generic bispectrum shapes, we show that, if not included in the modeling, the primary-lensing-Rees-Sciama contribution yields an effective f{sub NL} of 10 when using a bispectrum estimator optimized for local non-Gaussianity. Considering that expected 1-{sigma} errors on f{sub NL} are <10 from forthcoming experiments, we conclude that the contribution from this signal must be included in future constraints on f{sub NL} from the cosmic microwave background bispectrum.

  17. REE and other trace and major elements in the topsoil layer of Santiago island, Cape Verde

    NASA Astrophysics Data System (ADS)

    Marques, Rosa; Prudêncio, M. Isabel; Rocha, Fernando; Cabral Pinto, Marina M. S.; Silva, M. Manuela V. G.; Ferreira da Silva, Eduardo

    2012-02-01

    Geochemistry of major, trace and rare earth elements (REEs) of soils of Santiago island (Cape Verde) has been done in order to characterize soils developed on volcanic rocks and Quaternary sediments, contributing to the establishment of a geochemical atlas of the island. Sampling was made according to the recommendations of the IGCP 259 ("International Geochemical Mapping"). REE clearly differentiate soils with contrasting parent materials, particularly carbonatites-related soils, where lower MREE/LREE and MREE/HREE ratios were found, associated with higher contents of Ba, Th and U. Total contents of Cs, As and Ga are associated with the finer soils. The percentage of Fe, Co, Mn and Sc extracted using aqua regia increased with increase of the clay size proportion. Concerning potentially pollutant elements, As contents increase with decreasing particle size, and very high concentrations of Cr were found in some soils. However, As is less available in the finer soils and the percentages of extraction of Cr are low, limiting eventual environmental and health effects in the Santiago island.

  18. Discrimination of sediment provenance in the Yellow Sea: Secondary grain-size effect and REE proxy

    NASA Astrophysics Data System (ADS)

    Jung, Hoi-Soo; Lim, Dhongil; Jeong, Do-Hyun; Xu, Zhaokai; Li, Tiegang

    2016-06-01

    This study analyzed grain size and elemental concentrations (Al, Mg, Fe, and rare earth elements (REEs)) in 91 surface sediments to elucidate sediment provenance in the Yellow Sea. Elemental concentrations were normalized by Al concentration (Celement/CAl) to minimize the sediment grain-size effect (GSE). However, noticeable linear relationships between Al concentration (or mean grain size) and the ratio (e.g., Mg/Al or Fe/Al) appeared unexpectedly in pair diagrams. The spatial distribution patterns of Fe/Al and Mg/Al ratios were also similar to the pattern of mean grain size. This implies that the GSE was not removed completely, even after the normalization process. Thus, great care must be taken when applying the ratios of Celement/CAl as a proxy of sediment provenance. To improve provenance discrimination of the sediments in the Yellow Sea, the difference between the REE distribution patterns of Chinese and Korean river sediments, expressed as δ (δ = REE∗(La) - REE∗(Lu)), was calculated, and the spatial distribution patterns of the δ values were mapped. The δ values gradually increased from the western to the eastern part of the Yellow Sea, except for low δ values in the southeastern part of the Yellow Sea. This result indicates that the majority of Chinese and Korean river sediments are accumulating near to their respective coasts, except for a deposit along the southwestern coast of Korea in which a considerable amount of sediment from Chinese rivers has been accumulating.

  19. The evolution of immiscible silicate and fluoride melts: Implications for REE ore-genesis

    NASA Astrophysics Data System (ADS)

    Vasyukova, O.; Williams-Jones, A. E.

    2016-01-01

    The Mid-Proterozoic peralkaline Strange Lake pluton (Québec-Labrador, Canada) exhibits extreme enrichment in high field strength elements (HFSE), including the rare earth elements (REE), particularly in pegmatites. On the basis of a study of melt inclusions, we proposed recently that fluoride-silicate melt immiscibility played an important and perhaps dominant role in concentrating the REE within the pluton. Here we present further evidence for silicate-fluoride immiscibility at Strange Lake from a sample of the hypersolvus granite, which contains an inclusion composed largely of REE and HFSE minerals. The inclusion (∼5 cm in diameter) comprises a narrow rim containing chevkinite-(Ce) and zircon in a fluorite matrix, a core of fluorbritholite-(Ce) and bastnäsite-(Ce) and a transition zone between the rim and the core consisting of a fine-grained intergrowth of bastnäsite-(Ce), gagarinite-(Y) and fluorite. We propose that the inclusion formed as a result of silicate-fluoride immiscibility, which occurred early in the emplacement history of the Strange Lake pluton, and that it represents the fluoride melt. After separation of the two melts, the boundary between them acted as a locus of crystallisation, where crystals formed repeatedly due to heterogeneous (surface catalysed) nucleation. Zircon crystallised shortly after melt phase separation, and was followed by the growth of perthite together with arfvedsonite and quartz. As a result, the silicate melt surrounding the fluoride inclusion became enriched in volatiles that facilitated crystallisation of progressively larger crystals in the inclusion; large crystals of arfvedsonite and perthite were succeeded by even larger crystals of quartz. Massive crystallisation of chevkinite-(Ce) followed, forming the rim of the inclusion. The fluoride melt, which constituted the matrix to the silicate minerals and chevkinite-(Ce), crystallised after chevkinite-(Ce), forming fluorbritholite-(Ce) and fluorite. Aqueous fluid

  20. Al-26, Pu-244, Ti-50, REE, and trace element abundances in hibonite grains from CM and CV meteorites

    NASA Astrophysics Data System (ADS)

    Fahey, A. J.; Goswami, J. N.; McKeegan, K. D.; Zinner, E.

    1987-02-01

    Hibonites from the CM meteorites Murchison, Murray, and Cold Bokkeveld, and hibonites and Ti-rich pyroxene from the CV chondrite Allende are studied. Electron microprobe measurements of major element concentrations and track and ion probe measurements of Mg and Ti isotopic ratios, rare earth elements (REEs), and trace element abundances are analyzed. Correlations between isotopic anomalies in Ti, Al-26, Pu-244, and Mg-26(asterisk) are examined. Ti isotopic anomalies are compared with REE and trace element abundance patterns. Reasons for the lack of Al-26 in the hibonites are investigated and discussed. It is observed that there is no correlation between the Ti isotopic compositions, and the presence of Mg-26(asterisk), Pu-244, and REE and trace element patterns in individual hibonite samples. The data reveal that hibonites are not interstellar dust grains but formed on a short time scale and in localized regions of the early solar system.

  1. Al-26, Pu-244, Ti-50, REE, and trace element abundances in hibonite grains from CM and CV meteorites

    NASA Technical Reports Server (NTRS)

    Fahey, A. J.; Mckeegan, K. D.; Zinner, E.; Goswami, J. N.

    1987-01-01

    Hibonites from the CM meteorites Murchison, Murray, and Cold Bokkeveld, and hibonites and Ti-rich pyroxene from the CV chondrite Allende are studied. Electron microprobe measurements of major element concentrations and track and ion probe measurements of Mg and Ti isotopic ratios, rare earth elements (REEs), and trace element abundances are analyzed. Correlations between isotopic anomalies in Ti, Al-26, Pu-244, and Mg-26(asterisk) are examined. Ti isotopic anomalies are compared with REE and trace element abundance patterns. Reasons for the lack of Al-26 in the hibonites are investigated and discussed. It is observed that there is no correlation between the Ti isotopic compositions, and the presence of Mg-26(asterisk), Pu-244, and REE and trace element patterns in individual hibonite samples. The data reveal that hibonites are not interstellar dust grains but formed on a short time scale and in localized regions of the early solar system.

  2. U-Th-Pb ion microprobe analysis of monazite from the Paleoproterozoic Karrat rare earth element (REE) deposit, western Greenland

    NASA Astrophysics Data System (ADS)

    Mott, A.; Grove, M.; Bird, D. K.

    2012-12-01

    The Karrat rare earth element (REE) deposit is located at 72°N on the Niaqornakavsak peninsula of Qeqertarssuq Island on the western coast of Greenland. Metasomatic alteration of an amphibolite host rock by carbonatite derived fluids resulted in REE mineralization in the Karrat Isfjord area. REE in the mineralization are primarily found in bastnasite, allanite, and monazite. In-situ analysis of monazite was conducted on samples obtained from three sites of mineralization: (1) the primary deposit at Niaqornakavsak consisting of a single distinct ~30m thick unit; (2) at Umiamako Nuna 7 km to the east of Niaqornakavsak where the majority of REE mineralization occurs within the first 20m of the surface; and (3) a 6m thick REE-rich vein 100m below the surface at Umiamako Nuna. Formation ages for monazite at Niaqornakavsak, Umiamako Nuna (surface), and Umiamako Nuna (vein) have been calculated using 207Pb/206Pb, 206Pb/238U, and 208Pb/232Th isotope ratios. Multiple isotope ratios were examined to determine the ideal method of monazite analysis based on the inherent issues of low U content of monazite, difficulties measuring 204Pb, common Pb corrections, and peak interferences resulting from high concentrations of REE. 208Pb/232Th analysis resulted in the best precision and smallest spread of values. Energy filtering was applied to 208Pb/232Th analyses in an effort to reduce interferences at several peaks. Although all three isotope ratio analyses result in a Paleoproterozoic age similar to the timing of convergence of the North Atlantic craton, Rae craton, and Aasiat domain as well as the emplacement of the Prøven Igneous Complex in Greenland (1.95-1.80Ga), the values range between 1.7-1.9Ga depending on the isotope ratio.

  3. Closure temperature in cooling bi-mineralic systems: I. Definition and with application to REE-in-two-pyroxene thermometer

    NASA Astrophysics Data System (ADS)

    Yao, Lijing; Liang, Yan

    2015-08-01

    Closure temperature is an important concept to many diffusion related problems involving cooling. The basic idea and formulation were outlined in the seminal work of Dodson for cooling mono-mineralic systems. The Dodson's equation has been widely used to calculate closure temperatures for igneous and metamorphic rocks that contain more than one mineral. The purpose of this study is to examine closure temperatures in cooling bi-mineralic systems and to investigate the physical meaning of temperatures calculated using the REE-in-two-pyroxene thermometer. We conduct numerical simulations of diffusive redistribution of trace elements between two coexisting minerals under prescribed cooling using temperature-dependent diffusion coefficients and mineral-mineral partition coefficients. Following Dodson's treatment, the closure temperature in bi-mineralic systems can be defined by the evolution of either average trace element concentrations in the two minerals or their ratio. The latter defines an effective partition coefficient. Closure temperatures calculated based on the two definitions are compared for a range of cooling rates, grain sizes, mineral proportions, and temperature-dependent partition coefficients and diffusion coefficients. Temperatures defined by the effective partition coefficient are recommended. Application to diffusive redistribution of rare earth elements (REE) in orthopyroxene-clinopyroxene systems demonstrates that closure temperature differences among REE are small and hence their average value may be used as the closure temperature for the cooling two-pyroxene system. The average closure temperature of REE in the two-pyroxene system is essentially the same as the temperature calculated using the REE-in-two-pyroxene thermometer and practically independent of pyroxene modal abundance in the system. Differences in temperatures calculated using the REE- and major element-based two-pyroxene thermometers can be used to infer cooling rate of two

  4. Characterization of REE-Bearing Minerals and Synthetic Materials Using High Resolution Ultraviolet to Near-Infrared Reflectance Spectroscopy

    NASA Astrophysics Data System (ADS)

    Hoefen, T. M.; Livo, K. E.; Giles, S. A.; Lowers, H. A.; Swayze, G. A.; Taylor, C. D.; Verplanck, P. L.; Emsbo, P.; Koenig, A.; Mccafferty, A. E.

    2014-12-01

    Diagnostic crystal field 4fn-4fn transition features in the ultraviolet (UV) to near-infrared (NIR) region of the electromagnetic spectrum have been observed in many common rare earth element (REE)-bearing minerals. The partial filling of the 4f electron shell combined with a shielding effect caused by the fully filled 5s25p6-electron shells, which weaken any effects from external magnetic or electric fields on the electrons, makes rare earth ions unique. The narrow absorption features occur as a result of parity forbidden transitions and crystal field splitting of the trivalent REEs, and since they are well shielded, only subtle wavelengths shifts are seen in their spectral features. Synthetic single REE phosphates, carbonates, oxides, hydroxides and glasses have been measured in the lab to help identify absorption band positions that are characteristic of each REE as they occur in different minerals. Because spectral resolution is critical to identifying shifts in the absorption band positions, these materials have been measured on several different high resolution spectrometers. Using a combination of Ocean Optics USB 2000+ UV-VIS, USB2000+ VIS-NIR and ASD FS 4 spectrometers we have characterized REE-bearing materials from 0.2 to 2.5 microns with a spectral resolution of ~2 nm between 0.2 and 1.0 microns and 11 to 12 nm between 1.0 and 2.5 microns. Results to date suggest that wavelength shifts and variations in the degree of crystal field splitting allow spectral differentiation between REE-bearing minerals. To support these results, a comprehensive suite of marine phosphates, paleo-beach placers, IOCG deposits, alkaline to peralkaline igneous complexes, pegmatites associated with alkaline magmas and carbonatite intrusives, have been measured and included in our database. Core, rock chips, billets, sediment samples and grab samples were manually scanned to identify the most intense or spectrally different REE features. While REE-bearing minerals have been

  5. Pc 5 Spectral Density at ULTIMA stataions and its Radial Diffusion Coefficients for REE

    NASA Astrophysics Data System (ADS)

    Fujimoto, A.; Tokunaga, T.; Abe, S.; Uozumi, T.; Yoshikawa, A.; Mann, I. R.; Chi, P. J.; Engebretson, M. J.; Yumoto, K.

    2009-12-01

    Pc 5 magnetic pulsations with frequencies between 1.67 and 6.67 mHz, are believed to contribute to the Relativistic Electron Enhancement (REE) in the outer radiation belt during magnetic storms. Ground-based observations suggested that high-speed solar wind and large-amplitude Pc 5 waves with a long duration during the storm recovery phase are closely associated with the production of relativistic electrons [Baker et al., 1998; Rostoker et al., 1998; Mathie and Mann, 2000; O’Brien et al., 2001, 2003]. On the other hand, many relativistic electron acceleration mechanisms have been proposed theoretically. They are separated roughly into two themes: in situ acceleration at L lower than 6.6 by wave particle interactions (as internal source acceleration mechanisms) [Liu et al., 1999; Summers et al., 1999; Summers and Ma, 2000] and acceleration by radial diffusion to transport and accelerate a source population of electrons from the outer to the inner magnetosphere (as external source acceleration mechanisms) [Elkington et al., 1999, 2003; Hudson et al., 2000; Kim et al., 2001]. One possible external source acceleration mechanism is the resonant interaction with ULF toroidal and poloidal waves. In order to verify which of the two mechanisms is more effective for the REE, we have to examine the time variation of electron phase space density. Electron phase space density is not directly measured, but we can estimate radial diffusion coefficients using observational electric and magnetic data. The goal of this paper is to get more reliable radial diffusion coefficient from ground-based observational magnetic field and to show reasonability of it for radial diffusion model. We use the global magnetometer data obtained from ULTIMA (Ultra Large Terrestrial International Magnetic Array, see http://www.serc.kyushu-u.ac.jp/ultima/ultima.html) stations, to precisely define the radial diffusion timescales. The ULTIMA includes McMAC, CARISAM, 210MM and MAGDAS/CPMN magnetometer

  6. The Obtaining of Nano Oxide Systems SiO2-REE with Alkoxide Technology

    NASA Astrophysics Data System (ADS)

    Amelina, Anna; Grinberg, Evgenii

    A lot of oxides systems with REE as dopants are used in catalytic processes in organic synthesis. They are very perspectives as thermostable coating in aerospace technics. These systems are usually based on silicon or aluminium oxides and doped with rare-earth elements. This systems can be produced by different methods. One of the most perspective of them is “sol-gel”-method with silicium, aluminium and rare-earth alkoxides as a precursor of doped silica and alumina, or their derivatives. Thus the obtaining of composite SiO _{2} - REE oxide materials by the hydrolysis doped with rare-earth elements was suggested. Some of alcoholate derivatives such as El(OR)n were used in this processes. The SiO _{2}- REE oxides were precipitated during the sol-gel process, where tetraethoxysilane (TEOS) as used as SiO _{2} sources. Also it is known that alkoxides of alkali metals, including lithium alkoxides, are widely used in industry and synthetic chemistry, as well as a source of lithium in various mixed oxide compositions, such as lithium niobate, lithium tantalate or lithium silicate. Therefore, we attempted to obtain the lithium silicate, which is also doped with rare-earth elements. Lithium silicate was obtained by alkaline hydrolysis of tetraethoxysilane with lithium alkoxide. Lithium alkoxide were synthesized by dissolving at metal in the corresponding alcohol are examined. The dependence of the rate of dissolving of the metal on the method of mixing of the reaction mixture and the degree of metal dispersion was investigated. The mathematical model of the process was composed and also optimization of process was carried out. Some oxide SiO _{2}, Al _{2}O _{3} and rare-earth nanostructured systems were obtained by sol-gel-method. The size of particle was determined by electron and X-ray spectroscopy and was in the range of 5 - 15 nm. Purity of this oxide examples for contaminating of heavy metals consists n.(1E-4...1E-5) wt%. Sols obtained by this method may be used

  7. Geochemistry and microprobe investigations of Abu Tartur REE-bearing phosphorite, Western Desert, Egypt

    NASA Astrophysics Data System (ADS)

    Awadalla, Gamal S.

    2010-07-01

    Phosphorites in Egypt occur in the Eastern Desert, the Nile Valley and the Western Desert at Abu Tartur area and present in Duwi Formation as a part of the Middle Eastern to North African phosphogenic province of Late Cretaceous to Paleogene age (Campanian-Maastrichtian). The Maghrabi-Liffiya phosphorite sector is considered as the most important phosphorite deposits in the Abu Tartur area due to its large reserve thickness and high-grade of lower phosphorite bed beside high content of REE. Back scattered electron (BSE) images show framboidal pyrite filling the pores of the phosphatic grains, suggesting diagenetic reducing conditions during phosphorites formation. Electron Probe Micro Analyzer (EPMA) chemical mapping was conducted to examine the variation and distributions of selected elements (P, F, La, Fe, Yb, Si, Ce, W, Eu, S, Ca, Y and Er) within the shark teeth, coprolites and bone fragments. In the teeth W, S, Fe are concentrated along the axis of the teeth, the bone fragments show high concentration of W, Yb, Er and Eu, whereas coprolites are nearly homogenous in composition contains S, Er with some Si as micro-inclusions. Fluorapatite is considered as main phosphate mineral whereas pyrite occurs as pore-filling within the phosphatic grains and cement materials. Maghrabi-Liffiya samples show a wide range in the P 2O 5 content, between 19.8 wt.% and 29.8 wt.% with an average of 24.6 wt.% and shows low U content ranging from 15 ppm to 34 ppm with an average of 22 ppm. The total REE content in nine samples representing the Maghrabi-Liffiya ranges from 519 to 1139 ppm with an average of about 879 ppm. The calculation of LREE (La-Gd) show indeed a marked enrichment relative to the HREE (Tb-Lu) where LREE/HREE ratio attains 8.4 indicating a strong fractionation between the LREE and HREE. Chondrite-normalized REE patterns of the studied phosphorite samples show a negative Eu anomaly.

  8. ``From Fundamental Motives to Rational Expectation Equilibrium[REE, henceworth] of Indeterminacy''

    NASA Astrophysics Data System (ADS)

    Maksoed, Ssi, Wh-

    For ``Principle of Indeterminacy''from Heisenberg states: ``one of the fundamental cornerstone of quantum mechanics is the Heisenberg uncertainty principle''.whereas canonically conjugate quantities can be determined simultaneously only with a characteristic indeterminacy[M. Arevalo Aguilar, et.al]. Accompanying Alfred North Whitehead conclusion in ``The Aims of Education''that mathematical symbols are artificial before new meanings given, two kinds of fundamental motives: (i) expectation-expectation, (ii) expectation-certainty inherently occurs with determinacy properties of rational expectation equilibrium(REE, henceworth)- Guido Ascari & Tizano Ropele:''Trend inflation, Taylor principle & Indeterminacy'', Kiel Institute, June 2007. Furthers, relative price expression can be compare of their α and (1 - α) configurations in the expression of possible activity. Acknowledgment to Prof[asc]. Dr. Bobby Eka Gunara for ``made a rank through physics'' denotes...

  9. Carbonatites of the World, Explored Deposits of Nb and REE - Database and Grade and Tonnage Models

    USGS Publications Warehouse

    Berger, Vladimir I.; Singer, Donald A.; Orris, Greta J.

    2009-01-01

    This report is based on published tonnage and grade data on 58 Nb- and rare-earth-element (REE)-bearing carbonatite deposits that are mostly well explored and are partially mined or contain resources of these elements. The deposits represent only a part of the known 527 carbonatites around the world, but they are characterized by reliable quantitative data on ore tonnages and grades of niobium and REE. Grade and tonnage models are an important component of mineral resource assessments. Carbonatites present one of the main natural sources of niobium and rare-earth elements, the economic importance of which grows consistently. A purpose of this report is to update earlier publications. New information about known deposits, as well as data on new deposits published during the last decade, are incorporated in the present paper. The compiled database (appendix 1; linked to right) contains 60 explored Nb- and REE-bearing carbonatite deposits - resources of 55 of these deposits are taken from publications. In the present updated grade-tonnage model we have added 24 deposits comparing with the previous model of Singer (1998). Resources of most deposits are residuum ores in the upper part of carbonatite bodies. Mineral-deposit models are important in exploration planning and quantitative resource assessments for two reasons: (1) grades and tonnages among deposit types vary significantly, and (2) deposits of different types are present in distinct geologic settings that can be identified from geologic maps. Mineral-deposit models combine the diverse geoscience information on geology, mineral occurrences, geophysics, and geochemistry used in resource assessments and mineral exploration. Globally based deposit models allow recognition of important features and demonstrate how common different features are. Well-designed deposit models allow geologists to deduce possible mineral-deposit types in a given geologic environment, and the grade and tonnage models allow economists to

  10. Preservation of REE and Fe isotopes in altered stromatolites and the paleo-environmental record

    NASA Astrophysics Data System (ADS)

    Nies, S. M.; Shapiro, R. S.; Lalonde, S.

    2015-12-01

    Geochemical proxies are increasingly being used to unravel ancient ecosystems and environmental perturbations back to the earliest rock record on Earth. Along with more traditional fossils (stromatolites) and other biosignatures (e.g., lipids), the geochemical record is used specifically to evaluate biogenecity and to understand oxygenation of the atmosphere and ocean in the Archean and Paleoproterozoic. However, the effects of diagenesis, metamorphism, and other modes of secondary alteration are still poorly constrained, particularly as technological advances allow us to expand farther across the periodic table. Our study focused on the robustness and preservation of rare earth element (REE) and Fe isotope compositions of two stromatolitic units that have undergone contact and regional metamorphism. 18 samples were collected from cores, open pit mines, and field locations in Minnesota and Ontario from silicified iron formation (Biwabik-Gunflint formations). The samples were carefully constrained to one of two meter-scale stromatolitic units. Metamorphic grade ranged from essentially unmetamorphosed through prehnite-pumpellyite up to amphibolite (fayalite+hypersthene). Samples were also collected that represented deep secondary weathering, likely related to Cretaceous climatic extremes. Polished samples were first analyzed by electron microprobe and selected samples were further analyzed via laser ablation HR-ICP-MS to constrain trace element (n=13) and Fe isotopic variations (n=8). Preliminary results indicate that transition metal concentrations are surprisingly resilient to high-temperature metamorphic recrystallization. REE concentrations were analyzed in individual iron oxide grains, with full resolution (La to Lu) achieved for some samples and partial resolution (La to Nd) achieved for all samples. Core samples exhibited a relatively stable positive Ce anomaly occurring from low to extremely high alteration. Outcrop and mine samples indicate a shift from a

  11. Y,REE,Nb,Ta,Ti-oxide (AB 2O 6) minerals from REL-REE euxenite-subtype pegmatites of the Třebíč Pluton, Czech Republic; substitutions and fractionation trends

    NASA Astrophysics Data System (ADS)

    Škoda, Radek; Novák, Milan

    2007-04-01

    Aeschynite-group minerals (AGM) and euxenite-group minerals (EGM) occur in REL-REE euxenite-subtype pegmatites from the Třebíč Pluton, Czech Republic. They form strongly metamictized, light brown to black, equigranular to needle-like, subhedral to anhedral grains enclosed in blocky K-feldspar and less commonly in albite, and blocky quartz, and in the graphic unit (quartz and K-feldspar). Both AGM and EGM are homogeneous to slightly heterogeneous in BSE images. They are not commonly associated with the other primary Y,REE,Ti,Nb-bearing minerals, i.e. allanite-(Ce), monazite-(Ce), titanite, and ilmenite, which occur within the same textural-paragenetic unit. Aeschynite-(Y), aeschynite-(Ce), aeschynite-(Nd), nioboaeschynite-(Ce), tantalaeschynite-(Ce), vigezzite and polycrase-(Y) were identified using EMP and canonical discrimination analysis [Ercit, T.S., 2005a. Identification and alteration trends of granitic-pegmatite-hosted (Y,REE,U,Th)-(Nb,Ta,Ti) oxide minerals: a statistical approach. Can. Mineral. 43, 4 1291-1303.]. The exchange vector ACa B(Nb,Ta) A(Y,REE) - 1 BTi - 1 or its combination with the exchange vector ACa 2B(Nb,Ta) 3A(U,Th) - 1 A(Y,REE) - 1 BTi - 3 have been elucidated for the AGM. The exchange vector ACa A(U,Th) A(Y,REE) - 2 is predominant in the EGM. The AGM are enriched in HREE, whereas LREE are concentrated in the EGM. Weak to none-existent geochemical fractionations, as expressed by the U/(U + Th), Y/(Y + REE), Ta/(Ta + Nb) and (Nb + Ta)/(Ti + Nb + Ta) ratios, were noted for single grains from both the AGM and EGM, as well as in grains of polycrase-(Y) from four different textural-paragenetic units located in the Vladislav pegmatite. Simultaneous increase of U/(U + Th) and Y/(Y + REE) in the AGM during fractionation is typical. The Ta/(Ta + Nb) fractionation is usually weak and contradicts the Y/(Y + REE) and U/(U + Th) fractionation trends. This unusual behavior of Nb and Ta may be controlled by associated Ti-rich minerals (titanite

  12. REE Sorption Study of Sieved -50 +100 mesh Media #1 in Brine #1 with Different Starting pH's at 70C

    SciTech Connect

    Gary Garland

    2015-07-21

    This dataset described shaker table experiments ran with sieved -50 +100 mesh media #1 in brine #1 that have 2ppm each of the 7 REE metals at different starting pH's of 3.5, 4.5, and 5.5. The experimental conditions are 2g media to 150mL of REE solution, at 70C.

  13. Using Rare Earth Element (REE) tracers to identify perferential micro-sites of post-fire aeolian erosion

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Plant communities in desert environments are spatially anisotropic. We applied Rare Earth Element (REE) tracers to different landscape positions of an anisotropic Northern Chihuahua Desert ecosystem in an effort to study preferential sediment source areas. We delineated three 0.5 m by 6 m plots of...

  14. Submarine groundwater discharge is an important net source of light and middle REEs to coastal waters of the Indian River Lagoon, Florida, USA

    NASA Astrophysics Data System (ADS)

    Johannesson, Karen H.; Chevis, Darren A.; Burdige, David J.; Cable, Jaye E.; Martin, Jonathan B.; Roy, Moutusi

    2011-02-01

    Porewater (i.e., groundwater) samples were collected from multi-level piezometers across the freshwater-saltwater seepage face within the Indian River Lagoon subterranean estuary along Florida's (USA) Atlantic coast for analysis of the rare earth elements (REE). Surface water samples for REE analysis were also collected from the water column of the Indian River Lagoon as well as two local rivers (Eau Gallie River, Crane Creek) that flow into the lagoon within the study area. Concentrations of REEs in porewaters from the subterranean estuary are 10-100 times higher than typical seawater values (e.g., Nd ranges from 217 to 2409 pmol kg -1), with submarine groundwater discharge (SGD) at the freshwater-saltwater seepage face exhibiting the highest REE concentrations. The elevated REE concentrations for SGD at the seepage face are too high to be the result of simple, binary mixing between a seawater end-member and local terrestrial SGD. Instead, the high REE concentrations indicate that geochemical reactions occurring within the subterranean estuary contribute substantially to the REE cycle. A simple mass balance model is used to investigate the cycling of REEs in the Indian River Lagoon and its underlying subterranean estuary. Mass balance modeling reveals that the Indian River Lagoon is approximately at steady-state with respect to the REE fluxes into and out of the lagoon. However, the subterranean estuary is not at steady-state with respect to the REE fluxes. Specifically, the model suggests that the SGD Nd flux, for example, exported from the subterranean estuary to the overlying lagoon waters exceeds the combined input to the subterranean estuary from terrestrial SGD and recirculating marine SGD by, on average, ˜100 mmol day -1. The mass balance model also reveals that the subterranean estuary is a net source of light REEs (LREE) and middle REEs (MREE) to the overlying lagoon waters, but acts as a sink for the heavy REEs (HREE). Geochemical modeling and

  15. Sm-Nd dating and REE Composition of scheelite for the Honghuaerji scheelite deposit, Inner Mongolia, Northeast China

    NASA Astrophysics Data System (ADS)

    Guo, Zhijun; Li, Jinwen; Xu, Xinying; Song, Zeyou; Dong, Xuzhou; Tian, Jing; Yang, Yuncheng; She, Hongquan; Xiang, Anping; Kang, Yongjian

    2016-09-01

    Sm-Nd analyses of seven scheelite samples from scheelite-quartz veins in the Honghuaerji scheelite deposit produce a well-defined linear array on an isochron diagram with a mean square weighted deviation (MSWD) of 0.87 corresponding to an age of 178.4 ± 2.9 Ma with εNd(t) = + 1.50. This age is interpreted to represent the age of scheelite mineralization. The scheelite Sm-Nd age is in good agreement with U-Pb ages obtained from a mineralization-related granite (179.4 ~ 178.6 Ma), indicating that there is no apparent age gap between granite crystallization and ore formation. Rare earth element (REE) abundances in the scheelite were determined by in situ laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), and the scheelite samples contain elevated REE concentrations with total ΣREE + Y contents in the range of 3339 to 6321 ppm. The chondrite-normalized REE distribution patterns of all scheelites are middle REE (MREE)-enriched, with strong negative Eu-anomalies (Eu/Eu* = 0.09 ~ 0.23). The REE characteristics of the Honghuaerji scheelite suggest that REE3 + substituted into the Ca site along with Na and Nb (dominated by Na), whereas Eu is predominantly present as Eu2 + in the scheelite and may have crystallized from relatively reduced fluids. All sulfur isotope data (δ34S) for sulfide separates range from + 2.0 to + 3.8‰, with an average of 3.2‰. Measured 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios vary from 18.243 to 18.451, 15.494 to 15.574, and 37.933 to 38.340, respectively. On the basis of common Sr-Nd-Pb-Hf isotopic characteristics between the scheelite and the host granite and the positive initial Nd isotope ratios (+ 1.46 - + 1.52), low 87Sr/86Sr ratios (0.704983-0.705297) in the scheelites, it is inferred that the hydrothermal fluids responsible for tungsten mineralization at Honghuaerji were of magmatic origin with a mantle-derived signature. Based on the regional geology, tectonic evolution, and geochemical evidence, the

  16. Closure Temperature in Cooling Bi-Mineralic Systems With Application to REE-in-Two-Pyroxene Thermometer

    NASA Astrophysics Data System (ADS)

    Yao, L.; Liang, Y.

    2013-12-01

    Closure temperature is an important concept to many diffusion related problems involving cooling. The basic idea and formulation were outlined in the seminal work of Dodson for cooling mono-mineralic systems [1, 2]. The Dodson's equation has been widely used to calculate closure temperatures for igneous and metamorphic rocks that usually contain more than one mineral. The purpose of this study is to systematically examine closure temperatures in cooling bi-mineralic systems. This study is also motivated by our quest for the physical meaning of temperatures derived from the REE-in-two-pyroxene thermometer that is based on temperature-dependent REE partitioning between coexisting orthopyroxene (opx) and clinopyroxene (cpx) in mafic and ultramafic rocks [3]. To better understand closure temperatures and their relations to the REE-in-two-pyroxene thermometer, we conduct numerical simulations of diffusive re-equilibration of trace elements between two coexisting minerals under prescribed cooling using temperature-dependent diffusion coefficient and partition coefficient. Following Dodson's approach for mono-mineralic systems, we define the closure temperature of a trace element in cooling bi-mineralic systems using two methods: (1) by following the evolution of average concentration of the trace element in each mineral; (2) by tracing the variation of an effective partition coefficient (ratio of the average concentrations between the two minerals). Closure temperatures calculated using the two definitions are identical for a wide range of grain sizes and cooling rates. Additional simulations for a range of temperature-dependent partition coefficients and diffusion coefficients reveal that in addition to parameters introduced in Dodson's equation (pre-exponential factor D0, activation energy E, mineral grain size, and cooling rate), temperature-dependent partition coefficients are also important in determining the closure temperature for the bi-mineralic systems. Our

  17. The role of pegmatites and acid fluids for REE/HFSE mobilization in the Strange Lake peralkaline granitic pluton, Canada

    NASA Astrophysics Data System (ADS)

    Gysi, A. P.; Williams-Jones, A.

    2012-12-01

    The Strange Lake pluton in Canada is a mid-Proterozoic peralkaline granitic intrusion that is host to a world-class rare earth element (REE), yttrium (Y) and high-field strength element (HFSE) deposit containing more than 50 Mt ore at >1.5 wt.% REE and >3 wt.% Zr. The highest REE/HFSE concentrations are found in pegmatite-rich zones characterized by intense alteration. Previous studies of Strange Lake and other peralkaline and alkaline intrusions, such as Khan Bogd (Mongolia) and Tamazeght (Morocco) plutons have shown that hydrothermal alteration may play an important role in the mobility of the REE/HFSE. However, the fluid chemistry and conditions of alteration (i.e., P, T, pH, fO2, ligand activity) in these systems still need to be constrained to evaluate the importance and scale of such hydrothermal mobilization. We present new data from the B-zone, a pegmatite-rich zone located in NW Strange Lake. The pegmatites are generally zoned and form two main types. The border-type pegmatites consist of quartz, K-feldspar and hematized aegirine, whereas volatile-rich pegmatites consist of hydrothermal quartz and fluorite. Transitions between both types were also observed, with the K-feldspar being partly altered and replaced by Al-Si-rich phyllosilicates. The heavy (H)REE and Zr were primarily concentrated in zirconosilicates such as elpidite, now pseudomorphed by zircon or gittinsite, whereas light (L)REE and Y were concentrated in REE-F-(CO2)-minerals such as fluocerite and bastnäsite. Textural and mineralogical observations indicate that these minerals are primary and were partly to completely leached upon fluid-rock interaction in the pegmatites. Secondary phases include Ca-F-Y-rich minerals, mainly hydrothermal fluorite, that fill vugs and replaced primary REEHFSE minerals. The presence of hydrothermal fluorite veins, micro-veins, vugs and micro-breccia in the most altered parts of the B-zone are interpreted to reflect interaction of the rocks with a F-rich fluid

  18. Hydrothermal mobilization of pegmatite-hosted REE and Zr at Strange Lake, Canada: A reaction path model

    NASA Astrophysics Data System (ADS)

    Gysi, Alexander P.; Williams-Jones, Anthony E.

    2013-12-01

    Petrological and geochemical observations of pegmatites in the Strange Lake pluton, Canada, have been combined with numerical simulations to improve our understanding of fluid-rock interaction in peralkaline granitic systems. In particular, they have made it possible to evaluate reaction paths responsible for hydrothermal mobilization and mineralization of rare earth elements (REE) and Zr. The focus of the study was the B-Zone in the northwest of the pluton, which contains a pegmatite swarm and is the target of exploration for an economically exploitable REE deposit. Many of the pegmatites are mineralogically zoned into a border consisting of variably altered primary K-feldspar, arfvedsonite, quartz, and zirconosilicates, and a core rich in quartz, fluorite and exotic REE minerals. Textural relationships indicate that the primary silicate minerals in the pegmatites were leached and/or replaced during acidic alteration by K-, Fe- and Al-phyllosilicates, aegirine, hematite, fluorite and/or quartz, and that primary zirconosilicates (e.g., elpidite) were replaced by gittinsite and/or zircon. Reaction textures recording coupled dissolution of silicate minerals and crystallization of secondary REE-silicates indicate hydrothermal mobilization of the REE. The mobility of the light (L)REE was limited by the stability of REE-F-(CO2)-minerals (basnäsite-(Ce) and fluocerite-(Ce)), whereas zirconosilicates and secondary gadolinite-group minerals controlled the mobility of Zr and the heavy (H)REE. Hydrothermal fluorite and fluorite-fluocerite-(Ce) solid solutions are interpreted to indicate the former presence of F-bearing saline fluids in the pegmatites. Numerical simulations show that the mobilization of REE and Zr in saline HCl-HF-bearing fluids is controlled by pH, ligand activity and temperature. Mobilization of Zr is significant in both saline HF- and HCl-HF-bearing fluids at low temperature (250 °C). In contrast, the REE are mobilized by saline HCl-bearing fluids

  19. Reaction of seawater with fresh mid-ocean ridge gabbro creates ';atypical' REE pattern and high REE fluid fluxes: Experiments at 425 and 475 °C, 400 and 1000 bar

    NASA Astrophysics Data System (ADS)

    Beermann, O.; Garbe-Schönberg, D.; Holzheid, A. D.

    2013-12-01

    High-temperature MOR hydrothermalism significantly affects ocean chemistry. The Sisters Peak (SP) hydrothermal field at 5°S on the slow-spreading Mid-Atlantic Ridge (MAR) emanates fluids >400°C [1] that have high concentrations of H2, transition metals, and rare earth elements (REE) exhibiting ';atypical' REE pattern characterized by depletions of LREE and HREE relative to MREE and no Eu anomaly [2]. This is in contrast to the ';typical' LREE enrichment and strong positive Eu anomaly known from many MOR vent fluids observed world-wide [e.g., 3]. Besides temperature, the seawater-to-rock ratio (w/r ratio) has significant control on the fluid chemistry [e.g., 4, 5]. To understand how vent fluid REE-signatures are generated during water-rock interaction processes we reacted unaltered gabbro with natural bottom seawater at 425 °C and 400 bar and at 425 and 475 °C at 1000 bar at variable w/r (mass) ratios ranging from 0.5-10 by using cold seal pressure vessels (CSPV). The run durations varied from 3-72 h. Reacted fluids were analysed for major and trace elements by ICP-OES and ICP-MS. In our experiments, ';atypical' REE fluid pattern similar to those of SP fluids were obtained at high w/r ratio (5 and 10) that might be characteristic for focused fluid-flow along e.g., detachment faults at slow-spreading MOR [6]. In contrast, more ';typical'-like REE pattern with elevated LREE and slightly positive Eu anomalies have been reproduced at low w/r ratio (0.5-1). Results of numerical simulations imply that strong positive Eu anomalies of fluids and altered gabbro from high temperature MOR hydrothermal systems can be created by intense rock leaching processes at high w/r ratio (5-10). This suggests that hydrothermal circulation through the ocean crust creates ';typical' REE fluid pattern with strong positive Eu anomalies if seawater reacts with gabbroic host rock that has been already leached in REE at high fluid fluxes. Simulations of the temporal chemical evolution of

  20. Multistage metasomatism in lithospheric mantle beneath V. Grib pipe (Arkhangelsk diamondiferous province, Russia): evidence from REE patterns in garnet xenocrysts.

    NASA Astrophysics Data System (ADS)

    Shchukina, Elena; Alexei, Agashev; Nikolai, Pokhilenko

    2015-04-01

    150 garnet xenocrysts from V. Grib kimberlite pipe were analyzed for major and trace elements compositions. 70 % of garnet belong to lherzolite field; 14 % - megacrysts and pyroxenites; 11 % - eclogites; 4 % - harzburgite; 1 % (1- wehrlite defined by Sobolev (1973). Harzburgite garnets: sinusoidal REE patterns Smn/Ern > 5 (5.2 - 19.8). low Y (0.5 - 3.9 ppm), Zr (1.1 - 44.6 ppm), Ti (54 - 1322 ppm). Wehrlite garnetd: close to sinusoidal REE patterns, Smn/Ern - 1.8. Megacrysts and pyroxenites garnets: normal REE patterns Smn/Ern < 1 (0.2 - 0.6), high TiO2 (0.9 - 1.3 wt %). Lherzolite garnets 70 % show four groups of REE patterns similar to peridotite xenoliths (Shchukina et al., 2013, 2015). 1-st contains MREE at С1 level, Sm/Ern - 0.03, La/Ybn - 0.002. increasing La -Yb range, low Y, Zr, Ti indicating residual nature. 2-nd: MREE at 2 - 13 chondrite units, Smn/Ern (0.16 - 0.98), La/Ybn - 0.001 - 0.040 and flat pattern from MREE to HREE. 3-rd -MREE at 5 - 14 chondrite units, Sm/Ern > 1 (1.05 - 4.81) La/Ybn - 0.010-0.051 increasing an hump at MREE decreasing to HREE. 4-th: sinusoidal REE, Sm/Ern 4.2 - 27.2. and harzburgite Y, Zr, Ti . Average Cr2O3 content increases from 2-nd to the 3-rd group (3.3 to 5.7 wt%) and 4th (7.9 wt %). Average Y/Zr decreases from 2-nd (0.6) to 3rd (0.2) and 4th group (0.08). REE and Y, Zr, Ti indicate the metasomatic origin of garnets of 2, 3. 4 groups. Modeling of TREfor equilibrated melts and fractional crystallization 2nd group close to Turyino field basalts and 3-rd - to Izmozero field picrites of Arkhangelsk diamondiferous province (ADP). Basing on geochemical data of garnet xenocrysts and garnets and clinopyroxenes in peridotites (Shchukina et al., 2013, 2015) we suppose at least 3 stage of high-temperature metasomatic enrichment. 1st stage - is enrichment of residual garnets (found only in peridotite garnets) in LREE by the influence of carbonatite melt close to the Mela field carbonatites of ADP. REE patterns in clinopyroxenes from

  1. Rare earth elements (REE) as natural and applied tracers in the catchment area of Gessental valley, former uranium mining area of Eastern Thuringia, Germany

    NASA Astrophysics Data System (ADS)

    Buechel, G.; Merten, D.; Geletneky, J. W.; Kothe, E.

    2003-04-01

    Between 1947 and 1990 about 113.000 t of uranium were excavated at the former uranium mining site of Ronneburg (Eastern Thuringia, Germany). The legacy consists of more than 200 million m^3 of metasedimentary rocks rich in organic matter, sulfides and heavy metals originally deposited in mining heaps at the surface. The metasedimentary rocks formed under anoxic conditions about a 400 Mio. years ago are now exposed to oxic conditions. The oxidation of markasite and pyrite results in the formation of H_2SO_4. The formation of acid mine drainage (AMD) leads to high concentrations of uranium, rare earth elements (REE) and other heavy metals in surface water, seepage water and groundwater. This mobilization is due to alteration enhanced by high microbial activity and low pH. The tolerance mechanisms towards heavy metal pollution of soil substrate and surface/groundwater has allowed the selection of microbes which have, e.g. specific transporter genes and which are associated to plants in symbiotic interactions like mycorrhiza. In order to follow the processes linking alteration of metasedimentary rocks to biological systems the use of tracers is needed. One group of such tracers occuring in high concentrations in the water phase at the Ronneburg mining site are the REE (La-Lu) which are featured by very similar chemical behaviour. They show smooth but continuous variations of their chemical behaviour as a function of atomic number. For seepage water of the waste rock dump Nordhalde - sampled over a period of two years - the shale normalized REE patterns show enrichment of heavy REE and only minor variations, although the concentration differs. At sampling points in the surface water and in groundwater rather similar REE patterns were observed. Thus, REE can be used as tracers to identify diffuse inflow of REE-rich acid mine drainage of the dumps into the creek and the sediments. The absolute concentrations of REE in the creek and in ground water are up to 1000 times

  2. How lithology and climate affect REE mobility and fractionation along a shale weathering transect of the Susquehanna Shale Hills Critical Zone Observatory

    NASA Astrophysics Data System (ADS)

    Ma, L.; Jin, L.; Dere, A. L.; White, T.; Mathur, R.; Brantley, S. L.

    2012-12-01

    Shale weathering is an important process in global elemental cycles. Accompanied by the transformation of bedrock into regolith, many elements including rare earth elements (REE) are mobilized primarily by chemical weathering in the Critical Zone. Then, REE are subsequently transported from the vadose zone to streams, with eventual deposition in the oceans. REE have been identified as crucial and strategic natural resources; and discovery of new REE deposits will be facilitated by understanding global REE cycles. At present, the mechanisms and environmental factors controlling release, transport, and deposition of REE - the sources and sinks - at Earth's surface remain unclear. Here, we present a systematic study of soils, stream sediments, stream waters, soil water and bedrock in six small watersheds that are developed on shale bedrock in the eastern USA to constrain the mobility and fractionation of REE during early stages of chemical weathering. The selected watersheds are part of the shale transect established by the Susquehanna Shale Hills Observatory (SSHO) and are well suited to investigate weathering on shales of different compositions or within different climate regimes but on the same shale unit. Our REE study from SSHO, a small gray shale watershed in central Pennsylvania, shows that up to 65% of the REE (relative to parent bedrock) is depleted in the acidic and organic-rich soils due to chemical leaching. Both weathering soil profiles and natural waters show a preferential removal of middle REE (MREE: Sm to Dy) relative to light REE (La to Nd) and heavy REE (Ho to Lu) during shale weathering, due to preferential release of MREE from a phosphate phase (rhabdophane). Strong positive Ce anomalies observed in the regolith and stream sediments point to the fractionation and preferential precipitation of Ce as compared to other REE, in the generally oxidizing conditions of the surface environments. One watershed developed on the Marcellus black shale in

  3. REE chemistry and Sm-Nd systematics of late Archean weathering profiles in the Fortescue Group, Western Australia

    NASA Technical Reports Server (NTRS)

    MacFarlane, A. W.; Danielson, A.; Holland, H. D.; Jacobsen, S. B.

    1994-01-01

    Two weathering profiles, each consisting of an upper, sericite-rich zone and a lower, chlorite-rich zone, are preserved between flows of the Mt. Roe Basalt in the Fortescue Group, Hamersley Basin, Western Australia. REE concentrations in samples from these two profiles, which originally developed ca 2,760 Ma, show large variations depending on stratigraphic position. LREE abundances and (La/Yb)N are greatest at depths of 3-6 m below the paleosurface of the Mt. Roe #1 profile and are somewhat lower in samples above this level. The LREEs reach concentrations 6-9 times greater than in the underlying basalt, and thus appear to have been mobilized downward in the paleosol and concentrated in its middle part. LREE concentrations in the #2 profile show a similar distribution but with a sharp increase in all REE concentrations within 50 cm of the paleosurface. The distinction between the REE profiles in the two paleosols may be related to the difference in the overlying material. The #1 paleosol is overlain by a few meters of sediments and then by basalt, whereas the #2 paleosol is directly overlain by basalt. The LREEs appear to have been mobilized both during chemical weathering of the parental basalt and during later lower-greenschist-facies metamorphism and metasomatism of the paleosols. Remobilization of the REEs during the regional metamorphism of the Fortescue Group is confirmed by a whole-rock Sm-Nd reference isochron of Mt. Roe #1 samples with an age of 2,151 +/- 360 Ma. Variable initial 143Nd/144Nd values of unweathered basalt samples which may represent the paleosol protolith prevents a confident determination of the magnitude of LREE mobility. Both the initial mobilization of the REEs during weathering and the metasomatic remobilization appear to have taken place under redox conditions where Ce was present dominantly as Ce3+, because Ce anomalies are not developed within the sericite zone samples regardless of concentration. Europium anomalies in the

  4. REE chemistry and Sm-Nd systematics of late Archean weathering profiles in the Fortescue Group, Western Australia.

    PubMed

    MacFarlane, A W; Danielson, A; Holland, H D; Jacobsen, S B

    1994-04-01

    Two weathering profiles, each consisting of an upper, sericite-rich zone and a lower, chlorite-rich zone, are preserved between flows of the Mt. Roe Basalt in the Fortescue Group, Hamersley Basin, Western Australia. REE concentrations in samples from these two profiles, which originally developed ca 2,760 Ma, show large variations depending on stratigraphic position. LREE abundances and (La/Yb)N are greatest at depths of 3-6 m below the paleosurface of the Mt. Roe #1 profile and are somewhat lower in samples above this level. The LREEs reach concentrations 6-9 times greater than in the underlying basalt, and thus appear to have been mobilized downward in the paleosol and concentrated in its middle part. LREE concentrations in the #2 profile show a similar distribution but with a sharp increase in all REE concentrations within 50 cm of the paleosurface. The distinction between the REE profiles in the two paleosols may be related to the difference in the overlying material. The #1 paleosol is overlain by a few meters of sediments and then by basalt, whereas the #2 paleosol is directly overlain by basalt. The LREEs appear to have been mobilized both during chemical weathering of the parental basalt and during later lower-greenschist-facies metamorphism and metasomatism of the paleosols. Remobilization of the REEs during the regional metamorphism of the Fortescue Group is confirmed by a whole-rock Sm-Nd reference isochron of Mt. Roe #1 samples with an age of 2,151 +/- 360 Ma. Variable initial 143Nd/144Nd values of unweathered basalt samples which may represent the paleosol protolith prevents a confident determination of the magnitude of LREE mobility. Both the initial mobilization of the REEs during weathering and the metasomatic remobilization appear to have taken place under redox conditions where Ce was present dominantly as Ce3+, because Ce anomalies are not developed within the sericite zone samples regardless of concentration. Europium anomalies in the

  5. Partition coefficients of Hf, Zr, and REE between phenocrysts and groundmasses

    NASA Technical Reports Server (NTRS)

    Fujimaki, H.; Tatsumoto, M.; Aoki, K.-I.

    1984-01-01

    Partition coefficients of Hf, Zr, and REE between olivine, orthopyroxene, clinopyroxene, plagioclase, garnet, amphibole, ilmenite, phlogopite, and liquid are presented. Samples consist of megacrysts in kimberlite, phenocrysts in alkaline basalts, tholeiitic basalts and andesitic to dacitic rocks, and synthetic garnet and clinopyroxene in Hawaiian tholeiites. The Hf-Lu and Zr-Lu elemental fractionations are as large as the Lu-Sm or Lu-Nd fractionation. The Hf and Zr partition coefficients between mafic phenocrysts and liquids are smaller than the Lu partition coefficients, but are similar to the Nd or Sm partition coefficients. The Hf and Zr partition coefficients between ilmenite, phlogopite, and liquid are larger than the Lu partition coefficients for these minerals and their corresponding liquids. The Hf-Zr elemental fractionation does not occur except for extreme fractionation involving Zr-minerals and extremely low fO2. These data have an important bearing on chronological and petrogenetic tracer studies involving the Lu-Hf isotopic system.

  6. Recombinant cancer vaccines and new vaccine targets. Interview by Jenaid Rees.

    PubMed

    Schlom, Jeffrey

    2013-10-01

    Interview by Jenaid Rees, Commissioning Editor Jeffrey Schlom obtained his PhD from Rutgers University (NJ, USA). After obtaining his PhD, he worked at Columbia University (NY, USA) before moving in 1973 to the National Cancer Institute, National Institutes of Health (MD, USA). Since then he has served as the Chief of several sections, including his present position as the Chief of the Laboratory of Tumor Immunology and Biology in the Center for Cancer Research which he has held for the past 30 years. During this period, he has worked as an Adjunct Professor at George Washington University (Washington, DC, USA), served on the Editorial Board of several journals and holds membership in a number of committees. He holds over 30 patents and patent applications in the areas of vaccines, tumor antigens and monoclonal antibodies and has received honors and awards throughout his career. Jeffrey Schlom has been involved in translational research involving the immunotherapy of a range of carcinomas and predominantly works in the areas of tumor immunology, mechanisms of tumor cell-immune cell interactions and immune mechanisms. He has recently been working on the design and characterization of recombinant vaccines for cancer therapy. PMID:24098990

  7. Age-Dependent Changes in Resting Energy Expenditure (REE): Insights from Detailed Body Composition Analysis in Normal and Overweight Healthy Caucasians.

    PubMed

    Geisler, Corinna; Braun, Wiebke; Pourhassan, Maryam; Schweitzer, Lisa; Glüer, Claus-Christian; Bosy-Westphal, Anja; Müller, Manfred J

    2016-01-01

    Age-related changes in organ and tissue masses may add to changes in the relationship between resting energy expenditure (REE) and fat free mass (FFM) in normal and overweight healthy Caucasians. Secondary analysis using cross-sectional data of 714 healthy normal and overweight Caucasian subjects (age 18-83 years) with comprehensive information on FFM, organ and tissue masses (as assessed by magnetic resonance imaging (MRI)), body density (as assessed by Air Displacement Plethysmography (ADP)) and hydration (as assessed by deuterium dilution (D₂O)) and REE (as assessed by indirect calorimetry). High metabolic rate organs (HMR) summarized brain, heart, liver and kidney masses. Ratios of HMR organs and muscle mass (MM) in relation to FFM were considered. REE was calculated (REEc) using organ and tissue masses times their specific metabolic rates. REE, FFM, specific metabolic rates, the REE-FFM relationship, HOMA, CRP, and thyroid hormone levels change with age. The age-related decrease in FFM explained 59.7% of decreases in REE. Mean residuals of the REE-FFM association were positive in young adults but became negative in older subjects. When compared to young adults, proportions of MM to FFM decreased with age, whereas contributions of liver and heart did not differ between age groups. HOMA, TSH and inflammation (plasma CRP-levels) explained 4.2%, 2.0% and 1.4% of the variance in the REE-FFM residuals, but age and plasma T3-levels had no effects. HMR to FFM and MM to FFM ratios together added 11.8% on to the variance of REE-FFM residuals. Differences between REE and REEc increased with age, suggesting age-related changes in specific metabolic rates of organs and tissues. This bias was partly explained by plasmaT3-levels. Age-related changes in REE are explained by (i) decreases in fat free mass; (ii) a decrease in the contributions of organ and muscle masses to FFM; and (iii) decreases in specific organ and tissue metabolic rates. Age-dependent changes in the REE

  8. Age-Dependent Changes in Resting Energy Expenditure (REE): Insights from Detailed Body Composition Analysis in Normal and Overweight Healthy Caucasians

    PubMed Central

    Geisler, Corinna; Braun, Wiebke; Pourhassan, Maryam; Schweitzer, Lisa; Glüer, Claus-Christian; Bosy-Westphal, Anja; Müller, Manfred J.

    2016-01-01

    Age-related changes in organ and tissue masses may add to changes in the relationship between resting energy expenditure (REE) and fat free mass (FFM) in normal and overweight healthy Caucasians. Secondary analysis using cross-sectional data of 714 healthy normal and overweight Caucasian subjects (age 18–83 years) with comprehensive information on FFM, organ and tissue masses (as assessed by magnetic resonance imaging (MRI)), body density (as assessed by Air Displacement Plethysmography (ADP)) and hydration (as assessed by deuterium dilution (D2O)) and REE (as assessed by indirect calorimetry). High metabolic rate organs (HMR) summarized brain, heart, liver and kidney masses. Ratios of HMR organs and muscle mass (MM) in relation to FFM were considered. REE was calculated (REEc) using organ and tissue masses times their specific metabolic rates. REE, FFM, specific metabolic rates, the REE-FFM relationship, HOMA, CRP, and thyroid hormone levels change with age. The age-related decrease in FFM explained 59.7% of decreases in REE. Mean residuals of the REE-FFM association were positive in young adults but became negative in older subjects. When compared to young adults, proportions of MM to FFM decreased with age, whereas contributions of liver and heart did not differ between age groups. HOMA, TSH and inflammation (plasma CRP-levels) explained 4.2%, 2.0% and 1.4% of the variance in the REE-FFM residuals, but age and plasma T3-levels had no effects. HMR to FFM and MM to FFM ratios together added 11.8% on to the variance of REE-FFM residuals. Differences between REE and REEc increased with age, suggesting age-related changes in specific metabolic rates of organs and tissues. This bias was partly explained by plasmaT3-levels. Age-related changes in REE are explained by (i) decreases in fat free mass; (ii) a decrease in the contributions of organ and muscle masses to FFM; and (iii) decreases in specific organ and tissue metabolic rates. Age-dependent changes in the REE

  9. Sorption of REE and TPE on sulfonated strong-acid cation exchanger KU-2 from multicomponent HNO{sub 3} solutions

    SciTech Connect

    Chuveleva, E.A.; Kharitonov, O.V.; Firsova, L.A.

    1995-05-01

    Sorption of rare earths (REE) from multicomponent systems is studied as a function of solution acidity (0.1-2.0 M) and temperature (20-70{degrees}C). The elution curves for REE and transplutonium-element (TPE) sorption pass through a maximum, the value of which increases with decreasing solution acidity. The selectivity order changes for Y. This phenomenon is explained. The separation coefficients Nd-M are determined for various [HNO{sub 3}]. In the range [H{sup +}] = 0.5-2.01 M, the separation coefficients become <1. The optimal conditions for REE and TPE sorption are determined.

  10. Geochemistry of banded iron formation (BIF) host rocks, Yishui county, North China : major element, REE and other trace element analyses

    NASA Astrophysics Data System (ADS)

    Moon, I.; Lee, I.; Yang, X.

    2013-12-01

    Banded iron formation (BIF) in Yishui area, Western Shangdong Province in North China was formed from late Archean to early Paleoproterizoic (2.6Ga-2.5Ga). Amphibolite, metasediment (schist, gneiss) and migmatitic granite consist of host rocks of the BIF in North China. To find characteristics of BIF host rocks, major element, rare earth element and trace element analyses of whole rocks were conducted. Major elements are analyzed using X-ray Fluorescene Spectrometer (XRF) and REE and trace elements are analyzed by Inductively Coupled Plazma Mass Spectrometer (ICP-MS). Amphibolites show large negative Eu anomalies ([Eu]/[Eu*]=0.91~0.99) and ranges of REE are ∑REE=305~380 ppm. LREE/HREE ratios are (La/Lu)cn=21.07~26.12. SiO2 contents are 35.1~44.2 wt% and some samples have high Loss On Ignition values ([LOI]=8.35-10.06 wt%) compared to other amphibolites. LOI value is related to water and volatile contents in the rocks and it reflects amphibolite got high degree of alteration. The Fe and Mg mobility effects are shown by Fe2O3/MgO ratios which are 4.7~5.7. The Mg# varies from 25.6 to 29.3. Migmatitic granites have various range of ∑REE=21~241 ppm. They show both Eu negative anomalies ([Eu]/[Eu*]=0.53~0.71) and positive Eu anomalies ([Eu]/[Eu*]=1.95). Migmatitic granites have high SiO2 contents (68.8~72.2 wt%) and Al2O3 (13.4~14.2 wt%) contents. They have relatively low TiO2 (<0.5 wt%), MgO ( <0.6 wt%) and P2O5 (<0.2 wt%) contents. Gneiss samples were collected either from core or from mine pit. Core samples have negative Eu anomalies ([Eu]/[Eu*]=0.27~0.62) and show enriched LREE than HREE ((La/Lu)cn=45.60~62.32). Mine pit samples have positive Eu anomalies ([Eu]/[Eu*]=1.64~2.87) and almost flatten pattern except Eu anomalies ((La/Lu)cn=2.19~2.37). Core samples have higher Al2O3, TiO2, Na2O and K2O contents than mine pit samples. But remarkably mine pit samples have high contents of Fe2O3 (>40.4 wt%). Schists are divided into two types following REE patterns. Some

  11. Audre's daughter: Black lesbian steganography in Dee Rees' Pariah and Audre Lorde's Zami: A New Spelling of My Name.

    PubMed

    Kang, Nancy

    2016-01-01

    This article argues that African-American director Dee Rees' critically acclaimed debut Pariah (2011) is a rewriting of lesbian poet-activist Audre Lorde's iconic "bio-mythography" Zami: A New Spelling of My Name (1982). The article examines how Rees' work creatively and subtly re-envisions Lorde's Zami by way of deeply rooted and often cleverly camouflaged patterns, resonances, and contrasts. Shared topics include naming, mother-daughter bonds, the role of clothing in identity formation, domestic abuse, queer time, and lesbian, gay, bisexual, and transgender legacy discourse construction. What emerges between the visual and written texts is a hidden language of connection--what may be termed Black lesbian steganography--which proves thought-provoking to viewers and readers alike. PMID:26914826

  12. Origin of REE-rich ferrocarbonatites in southern Siberia (Russia): implications based on melt and fluid inclusions

    NASA Astrophysics Data System (ADS)

    Prokopyev, Ilya R.; Borisenko, Alexander S.; Borovikov, Andrey A.; Pavlova, Galina G.

    2016-06-01

    Fe-rich carbonatites with a mineral assemblage of ankerite-calcite or siderite are widespread in southern Siberia, Russia. The siderite carbonatites are associated with F-Ba-Sr-REE mineralization and have a 40Ar/39Ar age of 117.2 ± 1.3 Ma. Melt and fluid inclusions suggest that the carbonatites formed from volatile-rich alkali- and chloride-bearing carbonate melts. Ankerite-calcite carbonatites formed from carbonatite melt at a temperature of more than 790 °C. The ferrocarbonatites (the second phase of carbonatite intrusion) formed from a sulfate-carbonate-chloride fluid phase (brine-melt) at >650 °C and ≥360 MPa. The brine-melt fluid phase had high concentrations of Fe and LREEs. A subsequent hydrothermal overprint contributed to the formation of economically important barite-Sr-fluorite-REE mineralization in polymict siderite breccia.

  13. Tectonic implications of REE, Th, and Sc analyses of metamorphosed mudstones, Boyden Cave roof pendant, Sierra Nevada, California

    SciTech Connect

    Hanson, A.D.; Girty, G.H. . Dept. of Geological Sciences)

    1993-04-01

    The Boyden Cave pendant is subdivided into an eastern sequence, chaotic unit, and western sequence. The western sequence has an outcrop width of about 2.5 km and consists of a metasandstone unit, calcsilicate schist unit, andalusite biotite schist unit, and marble unit all metamorphosed to amphibolite grade. Because of complex structural relationships, the stratigraphic thicknesses of these four units are unknown. Psammites within the metasandstone unit, on average, are composed of 85.5 [+-] 4.2% quartz, 8.1 [+-] 4.6% total feldspar, 4.8 [+-] 2.8% white mica, 1.4 [+-] 1.3% biotite, and 0.1 [+-] 0.2% epidote (N = 17). The authors analyzed 10 mudstone samples for major, trace, and REEs from the metasandstone and andalusite biotite schist units of the Boyden Cave pendant. Chondrite-normalized REE distribution patterns exhibit LREE-enrichment trends, and Eu anomalies that vary from 0.61 to 0.86, and average 0.69. Such patterns are characteristic of mudstones composed of continentally derived detritus and are consistent with the complete absence of volcanic material. A similar set of geochemical data was collected from the proposed correlative miogeoclinal units in the Nopah Range, SE California. REE distribution patterns for mudstones from the Stirling Quartzite Wood Canyon Formation, and Carrara Formation exhibit LREE-enrichment trends and Eu anomalies that vary from 0.65 to 0.75, and average 0.68. REE distribution patterns for samples collected from the Boyden Cave and Nopah Range are nearly identical in all aspects. On a La-Th-Sc diagram, data from the mudstones in the Boyden Cave pendant cluster with data from the Nopah Range. Thus, the authors conclude that their data are consistent with the proposed correlations suggested by R.A. Schweickert and M.M. Lahren, and that the western sequence of the Boyden Cave pendant may represent a displaced fragment of the Cordilleran miogeocline.

  14. Fingerprinting young ignimbrites in Dominica (Lesser Antilles): Constraints from bulk REEs, apatite chemistry, and U-Th zircon chronology

    NASA Astrophysics Data System (ADS)

    Frey, H. M.; Manon, M. R.; Brehm, S.

    2015-12-01

    Multiple methods of fingerprinting tephra deposits enable distinction of separate magma batches beneath the island of Dominica. Previous studies have invoked a single large batholith but apatite REE chemistry is inconsistent with generation of multiple ignimbrites by fractional crystallization. The crystal-rich, andesite-dacite (58-66 wt% SiO2) ignimbrites comprise the largest explosive eruption in the Caribbean in the last 200 kyr, erupting a magma volume >58 km3 (Carey and Sigurdsson, 1980). Although the ignimbrites appear to emanate from several vents, their broad similarity in bulk chemistry, phase assemblage (pl + opx + cpx + hbl + ilm + mag + zrn + ap), and mineral composition, has led previous workers to suggest that Dominica is underlain by a single large batholith eruptions younging from north to south. However, bulk REE chemistry, solution ICP-MS chemistry of individual apatite grains, and ion microprobe U-Th dating of zircon rims from pumice clasts suggest a more complex plumbing system. More than 150 pumice clasts from northernmost (Morne aux Diables), northern (Wesley, Pointe Ronde, Grand Savanne), central (Layou, Roseau, Rosalie), and southern (Grand Bay, Grand Fonde) ignimbrites were analyzed for bulk chemistry. Geographically controlled differences exist in the concavity of the middle-heavy REE (Dy*). In central Dominica, apatites from the more evolved Layou Ignimbrite are depleted in middle REE compared to the nearby Roseau Ignimbrite, belying a genetic relationship via fractional crystallization. U-Th zircon rim ages in the northernmost and northern deposits were in secular equilibrium (>350 ka), whereas the central and southern ignimbrites yielded several populations of crystallization ages: Layou (99±12 ka), Roseau (139±12 ka; 65±17 ka), and Grand Bay (107±15 ka; 211±61 ka). Collectively, these observations are consistent with partial melting of magma batches prior to eruption rather than fractional crystallization of a single magma chamber.

  15. Dr. von Braun, Dr. Mueller, and Dr. Rees at the Firing Room During the SA-6 Launch

    NASA Technical Reports Server (NTRS)

    1964-01-01

    This photograph depicts an intense moment during the SA-6 launch at the Firing Room. Dr. von Braun, Director of the Marshall Space Flight Center (MSFC) is at center; to his left is Dr. George Mueller, Associate Director for Marned Space Flight; and far right is Dr. Eberhard Rees, Director for Research and Development, MSFC. The SA-6, the sixth flight of the Saturn 1 vehicle, launched a S-IV stage (a second stage) and an Apollo boilerplate spacecraft.

  16. REE radiation fault model: a tool for organizing and communication radiation test data and construction COTS based spacebourne computing systems

    NASA Technical Reports Server (NTRS)

    Ferraro, R.; Some, R.

    2002-01-01

    The growth in data rates of instruments on future NASA spacecraft continues to outstrip the improvement in communications bandwidth and processing capabilities of radiation-hardened computers. Sophisticated autonomous operations strategies will further increase the processing workload. Given the reductions in spacecraft size and available power, standard radiation hardened computing systems alone will not be able to address the requirements of future missions. The REE project was intended to overcome this obstacle by developing a COTS- based supercomputer suitable for use as a science and autonomy data processor in most space environments. This development required a detailed knowledge of system behavior in the presence of Single Event Effect (SEE) induced faults so that mitigation strategies could be designed to recover system level reliability while maintaining the COTS throughput advantage. The REE project has developed a suite of tools and a methodology for predicting SEU induced transient fault rates in a range of natural space environments from ground-based radiation testing of component parts. In this paper we provide an overview of this methodology and tool set with a concentration on the radiation fault model and its use in the REE system development methodology. Using test data reported elsewhere in this and other conferences, we predict upset rates for a particular COTS single board computer configuration in several space environments.

  17. Direct determination of europium valence state by XANES in extraterrestrial merrillite: Implications for REE crystal chemistry and martian magmatism

    SciTech Connect

    Shearer, C.K.; Papike, J.J.; Burger, P.V.; Sutton, S.R.; McCubbin, F.M.; Newville, M.

    2012-03-15

    The relative proportion of divalent and trivalent Eu has proven to be a useful tool for estimating f{sub O{sub 2}} in various magmatic systems. However, in most cases, direct determination of the Eu valence state has not been made. In this study, direct determination of Eu valence by XANES and REE abundance in merrillite provide insights into the crystal chemistry of these phosphates and their ability to record conditions of magmatism. Merrillite strongly prefers Eu{sup 3+} to Eu{sup 2+}, with the average valence state of Eu ranging between 2.9 and 3 over approximately six orders of magnitude in f{sub O{sub 2}}. The dramatic shift in the REE patterns of merrillite in martian basaltic magmas, from highly LREE-depleted to LREE-enriched, parallels many other trace element and isotopic variations and reflects the sources for these magmas. The behavior of REE in the merrillite directly reflects the relationship between the eightfold-coordinated Ca1 site and adjacent sixfold Na and tetrahedral P sites that enables charge balancing through coupled substitutions.

  18. A study of REE and Pb, Sr and Nd isotopes in garnet-lherzolite xenoliths from Mingxi, Fujian Province

    USGS Publications Warehouse

    Wankang, H.; Junwen, W.; Basu, A.R.; Tatsumoto, M.

    1993-01-01

    The REE and Pb, Sr, Nd isotopes in three xenoliths from limburgite and scoria-breccias, including spinel-lherzolite, spinel-garnet-lherzolite and phlogopite-gamet-lherzolite, were analysed. The REE contents of the xenoliths are 1.3 to 3.3 times those of the chondrites with their REE patterns characterized by weak LREE depletion. The143Nd/144Nd values of whole rocks and minerals range from 0.51306 to 0.51345 with ??Nd=+ 8.2- +15.8,206Pb/204 Pb < 18.673, and207Pb/204Pb < 15.574. All this goes to show that the upper mantle in Mingxi at the depth of 67-82 km is a depleted mantle of MORB type, with87Sr/86 Sr ratios 0.70237-0.70390. In Nd-Sr diagram the data points of whole rocks are all out of the mantle array, implying that the xenoliths from Mingxi have more radiogenic Sr isotopes than those of the mantle array. ?? 1993 Institute of Geochemistry, Chinese Academy of Sciences.

  19. Tracing and tracking wastewater-derived substances in freshwater lakes and reservoirs: Anthropogenic gadolinium and geogenic REEs in Lake Paranoá, Brasilia

    NASA Astrophysics Data System (ADS)

    Merschel, Gila; Bau, Michael; Baldewein, Linda; Dantas, Elton Luiz; Walde, Detlef; Bühn, Bernhard

    2015-09-01

    Total and dissolved rare earth element (REEs) and U concentrations were determined for waters from Lake Paranoá (Brasilia, Brazil) sampled in the dry (November 2012) and wet seasons (July 2013). Shale-normalized REE patterns of all samples display the M-type lanthanide tetrad effect and large positive Gd anomalies, but only the total REE pool shows a positive Ce anomaly, possibly reflecting aeolian and/or fluvial input from surrounding laterites. The positive Gd anomaly increased strongly between 2012 and 2013. It reveals an anthropogenic dissolved Gd source that enters the lake with effluents from wastewater treatment plants, originating from the use of Gd-based contrast agents in magnetic resonance imaging. Because anthropogenic Gd is a tracer for other wastewater-derived substances, such as pharmaceuticals, REE geochemistry offers an inexpensive way to monitor the presence of wastewater-derived substances in the lake, which may be utilized as a drinking water reservoir in the near future.

  20. Partition coefficients for REE between garnets and liquids - Implications of non-Henry's Law behaviour for models of basalt origin and evolution

    NASA Technical Reports Server (NTRS)

    Harrison, W. J.

    1981-01-01

    An experimental investigation of Ce, Sm and Tm rare earth element (REE) partition coefficients between coexisting garnets (both natural and synthetic) and hydrous liquids shows that Henry's Law may not be obeyed over a range of REE concentrations of geological relevance. Systematic differences between the three REE and the two garnet compositions may be explained in terms of the differences between REE ionic radii and those of the dodecahedral site into which they substitute, substantiating the Harrison and Wood (1980) model of altervalent substitution. Model calculations demonstrate that significant variation can occur in the rare earth contents of melts produced from a garnet lherzolite, if Henry's Law partition coefficients do not apply for the garnet phase.

  1. Oxygen Fugacity of the Martian Mantle From Pyroxene/Melt Partitioning of REE

    NASA Technical Reports Server (NTRS)

    Musselwhite, D. S.; Jones, J. H.

    2003-01-01

    This study is part of an ongoing effort to calibrate the pyroxene/melt REE oxybarometer for conditions relevant to the martian meteorites. Redox variations have been reported among the shergottites. Wadhwa used the Eu and Gd augite/melt partitioning experiments of McKay, designed for the LEW86010 angrite, to infer a range of fo2 for the shergottites. Others inferred fo2 using equilibria between Fe-Ti oxides. There is fairly good agreement between the Fe-Ti oxide determinations and the estimates from Eu anomalies in terms of which meteorites are more or less oxidized. The Eu anomaly technique and the Fe-Ti oxide technique both essentially show the same trend, with Shergotty and Zagami being the most oxidized and QUE94201 and DaG 476 being the most reduced. Thus, the variation in fo2 appears to be both real and substantive. However, although the redox trends indicated by the two techniques are similar, there is as much as two log unit offset between the results of three researchers. One explanation for this offset is that the Eu calibration used for the shergottites was actually designed for the LEW86010 angrite, a silica-undersaturated basalt whose pyroxene (diopside) compositions are rather extreme. To correct this, experiments have been conducted on the redox relationship of Eu partitioning relative to Sm and Gd for pyroxene/melt compositions more relevant to Martian meteorites. We report here preliminary results for experiments on pigeonite/melt partitioning as a function of fO2.

  2. The effect of the water-to-rock ratio on REE distribution in hydrothermal fluids: An experimental study

    NASA Astrophysics Data System (ADS)

    Beermann, Oliver; Garbe-Schönberg, Dieter; Holzheid, Astrid

    2013-04-01

    High-temperature submarine MOR hydrothermalism creates high elemental fluxes into, and out of, oceanic lithosphere significantly affecting ocean chemistry. The Turtle Pits hydrothermal system discovered at 5° S on the slow-spreading Mid-Atlantic Ridge (MAR) in water depths of ~3000 m (~300 bar) emanates 'ultrahot' fluids > 400 ° C [1] with high concentrations of dissolved gases (e.g., H2), transition metals, and rare earth elements (REE). The normalised REE patterns of these 'ultrahot' fluids are uncommon as they exhibit depletions of LREE and no Eu-anomaly ('special' REE-signature in [2]), which is in contrast to the "typical" LREE enrichment and pronounced positive Eu-anomaly known from many MOR vent fluids observed world-wide [e.g., 3]. Although hydrothermal fluid REE-signatures may play a key role in understanding processes during water-rock interaction, only few experimental data have been published on REE distribution in seawater-like fluids reacted with rocks from the ocean crust [e.g., 4, 5]. Besides temperature, the seawater-to-rock ratio (w/r ratio) strongly affects water-rock reaction processes and, thus, has significant control on the fluid chemistry [e.g., 6, 7]. To understand how vent fluid REE-signatures are generated during water-rock interaction processes we designed a series of experiments reacting different fluid types with mineral assemblages from fresh, unaltered gabbro at 425 ° C and 400 bar using cold seal pressure vessels (CSPV). Mixtures of 125-500 μm-sized hand-picked plagioclase and clinopyroxene grains separated from unaltered gabbro reacted in gold capsules with 3.2 wt.% NaCl(aq) fluid (similar to seawater salinity), or with natural seawater. The w/r (mass) ratio ranged from 1 to 100 and the run durations were varied from 3 to 30 d in the NaCl(aq) experiments, and was 3 d in the seawater experiments. The reacted fluids were extracted after quenching and analysed by ICP-OES and ICP-MS. Only in the seawater experiments, the gabbro

  3. Evolution of the fluid in the REE-rich pegmatites of the Strange Lake pluton

    NASA Astrophysics Data System (ADS)

    Vasyukova, O.; Williams-Jones, A. E.

    2015-12-01

    Five types of aqueous inclusions are observed in the Mid-proterozoic peralkaline granites and pegmatites of the Strange Lake pluton (Québec-Labrador, Canada). From earliest to latest they are: primary aqueous inclusions associated with melt inclusions (type 1), with CH4 inclusions (types 2 a and b enriched in H2 and higher hydrocarbons respectively), and CO2 inclusions (type 3), primary aqueous inclusions, which show no apparent association with any gas-rich fluid (type 4) and secondary aqueous inclusions associated with mineral pseudomorphs (type 5). The salinity of the fluid decreases from the earliest type 1 (24.1 wt.% NaCl eq.) to type 2 a and b (21.2 and 14.2 wt.% NaCl eq. respectively), to type 3 (10.1 wt.% NaCl eq.) and type 4 inclusions (8.2 wt.% NaCl eq.). The salinity of type 5 inclusions is high, i.e., 16.6 wt.% NaCl eq.. The gas composition changes systematically from CH4 ± H2 in type 1 and 2a to CH4 + higher hydrocarbons in type 2b and to CO2 dominant type 3 inclusions. Most of the inclusions show re-equilibration texures ('implosion' halos). Another typical feature is a tendency to decrepitate at temperatures higher than 140-150 °C. The fluid evolution started with the exsolution of a saline aqueous liquid (~25 wt.% NaCl eq.) from the pegmatitic melt at a temperature of about 400 °C and a pressure around 1100 bars. Further evolution occurred due to cooling (isobaric) and oxidation of the fluid. Early initial oxidation led to formation of higher hydrocarbons by oxidative coupling of methane, and later, full-blown oxidation led to the production of CO2. The CO2 reacted with Na-rich fluid to form nahcolite, which caused a significant decrease in the apparent salinity down to a critical level, below which further oxidation led to an increase in the CO2/CH4 ratio and eventual disappearance of CH4. Isobaric cooling continued down to at least 150-170 °C, at which temperature the CO2 component was consumed to form REE-rich flurocarbonates. Nahcolite

  4. Towards Synthesis and Usage of Actinide-Bearing REE Phosphate age Standards: A Progress Report

    NASA Astrophysics Data System (ADS)

    Pyle, J. M.; Cherniak, D. J.

    2006-05-01

    Electron microprobe (EMP) dates result from a concentration-time unit conversion, so use of a concentration- based (rather than isotope-ratio based) fictive age standard is warranted. This observation has motivated our mineral synthesis program, aimed at producing actinide-doped REE phosphate EMP dating standards that meet the following criteria: 1) known concentrations of U, Th, and Pb; 2) homogeneous intragrain distribution of all components; 3) of suitable size, either as a single-crystal or polycrystalline sintered ceramic. Single-crystal synthesis of actinide-doped LaPO4 by flux-growth methods results in disproportionation of lanthanide and flux, alkali, and actinide components into phosphate and oxide phases, respectively, and flux- growth methods were abandoned. Actinide-doped La phosphate is successfully prepared by high-T annealing and hydrothermal processing of microcrystalline phosphate; both homogeneity and charge-balance of (Ca, Th, Pb)-bearing LaPO4 increase with increasing solvent acidity during cold-seal hydrothermal synthesis. A combination of pressing and high-T (1400° C) sintering transforms fine-grained (0.1-10 μm) run- products to ceramic pellets with 90-95% theoretical density. Our most recent runs focused on a target composition of La80(CaTh)17(CaU)2(PbTh)1PO4 processed with 6% 2M HCl at 820° C, 0.75 kbar for 1 week. The run products are 0.1-2 μm crystals identified by XRD as La-actinide phosphate solid solution. 2 μm grains (N=16) give a composition (mean±2 sd) of La79.77(1.26)(CaTh)17.87(1.00)(CaU)1.53(0.42)(PbTh)0.82(0.09)PO4. Th (8.07-9.13 wt. %) is homogeneous at the level of analytical precision, and the Pb concentration range (3500-4350 ppm) is restricted relative to untreated precipitate. Uranium concentration values are more variable (6500-10000 ppm). This run yields a fictive age of 702±4 Ma (mean±2 se), compared to the fictive age of 794 Ma for the target composition.

  5. REE geochemistry of 3.2 Ga BIF from the Mapepe Formation, Barberton Greenstone Belt, South Africa

    NASA Astrophysics Data System (ADS)

    Yahagi, T. R.; Yamaguchi, K. E.; Haraguchi, S.; Sano, R.; Teraji, S.; Kiyokawa, S.; Ikehara, M.; Ito, T.

    2012-12-01

    Banded iron formations (BIFs) are chemical sediments interbedded with Fe- and Si-rich layers, characteristically present in the early history of the Earth. A popular hypothesis for the formation of BIFs postulates that dissolved oxygen produced by photosynthesizers such as cyanobacteria oxidized dissolved ferrous Fe supplied by submarine hydrothermal activities. During precipitation of Fe-oxide minerals, phosphorus and rare earth elements (REEs) were most likely adsorbed on their surface. Therefore, chemical compositions of REEs that adsorbed onto Fe-oxide have useful information on the seawater chemistry at the time of deposition. Especially, information on the redox state of seawater and the extent of the contribution of hydrothermal activity during BIF deposition are expected to have been recorded. Occurrence of BIF has been traditionally tied to the chemical evolution of the atmosphere. Rise of atmospheric oxygen, or as known as GOE (Great Oxidation Event: e.g., Holland, 1994), has been widely believed to have occurred at around 2.4 Ga ago. Contrary, however, some studies have suggested that such oxygenation could have occurred much earlier (e.g., Hoashi et al., 2009). In this study, we used 3.2 Ga old BIF from the Mapepe Formation at the bottom of the Fig Tree Group of the Swaziland Supergroup in the northeastern part of the Barberton Greenstone Belt, South Africa. We aimed to constrain the marine environment, and by inference atmospheric environment, at the time of BIF deposition from REE geochemistry. Major elements and REE compositions of 37 samples were measured using XRF and ICP-MS, respectively. Samples with less than 1.0 wt% Al2O3 are considered to be "pure" BIFs with minimal amount of continental contamination, and are expected to have inherited marine REE signatures. Abundance of REE normalized by C1 chondrite for the analyzed samples commonly exhibits positive Eu anomaly and LREE

  6. Genesis of the Bayan Obo Fe-REE-Nb deposit: Evidences from Pb-Pb age and microanalysis of the H8 Formation in Inner Mongolia, North China Craton

    NASA Astrophysics Data System (ADS)

    Lai, Xiaodong; Yang, Xiaoyong; Liu, Yulong; Yan, Zhiqiang

    2016-04-01

    The Bayan Obo Fe-REE-Nb deposit is a world-largest REE deposit in Inner Mongolia, North China Craton. It also contains large Fe and Nb reserves. The REE ore body is hosted in H8 dolomite of the Bayan Obo Group. Depositional time and genesis of H8 dolomite are still controversial in addressing the genesis of the REE deposit. In this study, Pb-Pb age and geochemical features of carbonate minerals in H8 dolomite have been studied, providing constraints to genesis of H8 dolomite and the REE deposit. Results of Pb-Pb dating from unmetamorphosed and non-mineralized domains of the H8 dolomite well constrain the depositional age as 1619 ± 150 Ma, which is earlier than both REE ore and carbonatite dykes in the Bayan Obo region. This indicates that REE mineralization has characteristics of epigenetic origin. Geochemical data of carbonate minerals in H8 dolomite have low REE contents, distinctly distinguished from those carbonatitic dykes. However, the fine-grained H8 dolomite whole rocks have high REE contents, similar to those carbonatitic dykes. Mineral analysis suggests a close relationship between REE mineralization and calcite carbonatite dykes and related-derived fluids, which could transport a large amounts of REE. Integrated with these new geochronological and geochemical data, we draw conclusion that the Bayan Obo Group was a Proterozoic depositional succession, REE mineralization is as result of sedimentary carbonate rocks once being metasomatised by fluids derived from regional REE-rich calcite carbonatitic magma at depth.

  7. Variations in the neodymium and strontium isotopic composition and REE content of molluscan shells from the Cretaceous Western Interior seaway

    SciTech Connect

    Whittaker, S.G.; Kyser, T.K. )

    1993-08-01

    Rare earth element concentrations, [epsilon][sub ND](T) values, and strontium isotopic compositions of mollusc shells were used to trace variations in the neodymium and strontium isotopic composition of the epicontinental Late Cretaceous Western Interior seaway of North America. Rare earth element patterns are different in aragonite and calcite produced by the molluscs endemic to the seaway, indicating that either mineralogical control or possibly scavenging by organic films associated with the different phases of biogenic carbonate resulted in differential partitioning of the REEs from seawater during shell formation. The biogenic carbonate also may contain REEs associated with Fe-flocs trapped in the shells during growth, but these flocs cannot result in different REE patterns of aragonite and calcite produced by the molluscs. The neodymium isotopic composition of the Western Interior seaway is inferred to have varied 13 [epsilon]-units over 20 My as a result of incursions of seawater from the Arctic Ocean and Gulf of Mexico, river influx from tectonically active terranes, benthic diagenetic fluxes, and volcanic ash falls. Ash from a variety of volcanic centers in western North America was significant in producing rapid and marked changes in [sup 143]Nd/[sup 144]Nd ratios of the seaway, and abrupt regional variations in neodymium isotopic composition of the seaway make the construction of an accurate neodymium isotope evolution curve difficult for this basin. Strontium isotopic compositions of the mollusc shells indicate the [sup 87]Sr/[sup 86]Sr ratio of the Western Interior seaway was generally similar to contemporaneous oceans, although, periodically, the basin had strontium isotopic compositions distinct from contemporaneous seawater. 58 refs., 7 figs., 3 tabs.

  8. REE and Lu-Hf systematics of zircons from rapakivi granites and associated rocks of supercontinent Nuna (Columbia)

    NASA Astrophysics Data System (ADS)

    Ronkin, Yu. L.; Gerdes, A.; Maslov, A. V.

    2015-03-01

    The last of the rifting events at 1.37-1.45 Ga that is considered to have led to the final breakup of Nuna was recorded in most of its building blocks (Laurentia, Baltica, and Siberian craton). At the type locality for the Riphean on the western slope of the South Urals, this event was recognized as the Mashak igneous event (˜1380 Ma) and can be classified as a LIP based on the volumes of magma generated (total igneous volumes >0.05 × 106 km3). The emplacement of large volumes of A-type granitic plutons in Laurentia and northwestern Baltica (in the present coordinates) was almost synchronous with this event. In the South Urals, within the Bashkirian meganticlinorium, the processes of granite generation and emplacement during this time took place on a much smaller scale. Anorogenic granites of this region are represented by rapakivi granites of the Berdyaush massif. The first REE and Lu-Hf isotope data for zircons from rapakivi granites and associated rocks of the Berdyaush massif reveal almost identical Lu-Hf isotope ages (˜1383 Ma) of rapakivi granites, quartz syenitic diorites, and nepheline syenites. It was shown that these rocks, which were emplaced into the heterogeneous Proterozoic crust between the Early and Middle Riphean, have the Hf isotopic compositions and Lu-Hf model ages reflecting the contribution from crustal sources with ages of 2013-2219 Ma, whereas the associated gabbros indicate derivation from a source with the Lu-Hf ages of 1658 ± 1685 Ma and moderately depleted ɛHf(1383) of (4.1 ± 0.7-4.9 ± 0.6). The REE characteristics (ΣREE, Eu/Eu*, Ce/Ce*, Pr/Pr*, La/Lu) and Lu-Hf isotope systematics of zircons can be used to constrain the history and genetic evolution of supercontinents, e.g., supercontinent Nuna (Columbia) in particular.

  9. Donnan membrane speciation of Al, Fe, trace metals and REEs in coastal lowland acid sulfate soil-impacted drainage waters.

    PubMed

    Jones, Adele M; Xue, Youjia; Kinsela, Andrew S; Wilcken, Klaus M; Collins, Richard N

    2016-03-15

    Donnan dialysis has been applied to forty filtered drainage waters collected from five coastal lowland acid sulfate soil (CLASS) catchments across north-eastern NSW, Australia. Despite having average pH values<3.9, 78 and 58% of Al and total Fe, respectively, were present as neutral or negatively-charged species. Complementary isotope dilution experiments with (55)Fe and (26)Al demonstrated that only soluble (i.e. no colloidal) species were present. Trivalent rare earth elements (REEs) were also mainly present (>70%) as negatively-charged complexes. In contrast, the speciation of the divalent trace metals Co, Mn, Ni and Zn was dominated by positively-charged complexes and was strongly correlated with the alkaline earth metals Ca and Mg. Thermodynamic equilibrium speciation calculations indicated that natural organic matter (NOM) complexes dominated Fe(III) speciation in agreement with that obtained by Donnan dialysis. In the case of Fe(II), however, the free cation was predicted to dominate under thermodynamic equilibrium, whilst our results indicated that Fe(II) was mainly present as neutral or negatively-charged complexes (most likely with sulfate). For all other divalent metals thermodynamic equilibrium speciation calculations agreed well with the Donnan dialysis results. The proportion of Al and REEs predicted to be negatively-charged was also grossly underestimated, relative to the experimental results, highlighting possible inaccuracies in the stability constants developed for these trivalent Me(SO4)2(-) and/or Me-NOM complexes and difficulties in modeling complex environmental samples. These results will help improve metal mobility and toxicity models developed for CLASS-affected environments, and also demonstrate that Australian CLASS environments can discharge REEs at concentrations an order of magnitude greater than previously reported. PMID:26780135

  10. Geology, mineralogy and fluid inclusion data of the Kizilcaören fluorite barite REE deposit, Eskisehir, Turkey

    NASA Astrophysics Data System (ADS)

    Gültekin, Ali Haydar; Örgün, Yüksel; Suner, Fikret

    2003-01-01

    The Kizilcaören fluorite-barite-Rare Earth Element (REE) deposit occurs as epithermal veins and breccia fillings in altered Triassic metasandstones and Oligocene-Miocene pyroclastics adjacent to alkaline porphyritic trachyte and phonolite. This deposit is the only commercial source of REE and thorium in Turkey. Most of the fluorite-barite-REE mineralisation at Kizilcaören has been formed by hydrothermal solutions, which are thought to be genetically associated with alkaline volcanism. The occurrence of the ore minerals in vuggy cavities and veins of massive and vuggy silica indicate that the ore stage postdates hydrothermal alteration. The deposit contains evidence of at least three periods of hypogene mineralisation separated by two periods of faulting. The mineral assemblage includes fluorite, barite, quartz, calcite, bastnäsite, phlogopite, pyrolusite and hematite as well as minor amounts of plagioclase feldspar, pyrite, psilomelane, braunite, monazite, fluocerite, brockite, goethite, and rutile. Fluid inclusion microthermometry indicates that the barite formed from low salinity (0.4-9.2 equiv. wt% NaCl) fluids at low temperatures, between 105 and 230 °C, but fluorite formed from slightly higher salinity (<12.4 equiv. wt% NaCl) fluids at low and moderate temperatures, between 135-354 °C. The depositional temperature of bastnäsite is between 143-286 °C. The local coexistence of liquid- and vapour-rich inclusions suggests boiling conditions. Many relatively low-salinity (<10.0 equiv. wt% NaCl), low and moderate temperature (200-300 °C) inclusions might be the result of episodic mixing of deep-saline brines with low-salinity meteoric fluids. The narrow range of δ34S (pyrite and barite) values (2.89-6.92‰ CDT)suggests that the sulphur source of the hydrothermal fluids are the same and compatible with a volcanogenic sulphate field derived from a magmatic sulphur source.

  11. REE contents in agricultural soil of Sweden (GEMAS): Comparison of weak MMI® extraction with near total concentrations

    NASA Astrophysics Data System (ADS)

    Sadeghi, Martiya; Andersson, Madelen; Ladenberger, Anna; Uhlbäck, Jo; Mann, Alan; Turner, Nick

    2014-05-01

    Within the GEMAS project agricultural soil samples were analyzed for 52 elements by aqua regia extraction, 41 elements by XRF (total concentration), for 57 elements in a mobile metal ion (MMI®) extraction. In addition, 174 samples from Swedish agricultural soil were analyzed by ICP-AES and ICP-MS using sodium peroxide fusion (SPF). The aim of this study is to compare the content of Rare Earth Elements (REEs) and their extractability using the MMI® extraction and the sodium peroxide fusion (SPF) methods. The statistical comparison of both methods reveal that the median extractability for most of the REEs obtained by the MMI® method is less than 1%, with an extractability of 0.5% for Ce and La, and 0.9% for Nd. The median value of Ce by MMI extraction is 0.31 mg/kg while the median by SPF is 59.5 mg/kg. For La the median value by MMI extraction is 0.14 mg/kg and 29.4 mg/kg by SPF, and for Nd the median is 0.23 mg/kg and 26.5 mg/kg , by the MMI and SPF methods respectively. All data from the Swedish samples lie over the detection limit, except for Ce (13 sample) and Tb (5 sample). The graphs of cumulative proportions of REEs by the MMI® extraction and SPF methods show that the trend of REEs is likely to be similar in both methods. The only difference is that the MMI method shows higher proportions of Y compared to the SPF method, while there are higher proportions of Ce and La in the SPF method compared to MMI® . The elemental distribution maps for both methods indicate that the distinct distribution patterns are influenced by not only underlying parent material or lithologies but that there is also an effect from the geochemical behaviour of individual elements, their extractability, and by the content of clay-size fractions in soil.

  12. The distribution of anthropogenic REE in the Dutch distributaries of the Rhine: the role of suspended matter

    NASA Astrophysics Data System (ADS)

    Roskam, Gerlinde; Verheul, Marc; Klaver, Gerard; Bakker, Ingrid

    2014-05-01

    In nature rare earth elements (REE) occur in fixed ratios; contamination with a single rare earth element causes a clear deviation from the natural NASC normalized REE-patterns: an anomaly. REE are progressively used in many high technology products and processes. For example, gadolinium-containing chelates have been used since the '80s as contrasting agent in MRI-imaging. The pertaining anomaly is currently used as a tracer for distinguishing waste water from water unaffected by anthropogenic contamination. In the Dutch monitoring program in the Rhine-Meuse distributaries, total (10% HNO3 digested) and dissolved (< 0.45 µm) fractions in surface water are routinely analysed, and with two-week intervals suspended matter samples are collected with a centrifuge. Since 2008, the set of analysed elements was extended with REE, enabling this study. Lobith, the entry point of the River Rhine in The Netherlands, shows an annual oscillation in the magnitude of the lanthanum (La) anomaly. This positive La-anomaly was reported by Kulaksiz and Bau in 2011; they identified the point source as a production plant for catalysts used in petroleum refining in the German city of Worms. Since the spring of 2011, samarium (Sm) is used in the same process, resulting in matching La- and Sm-anomalies. The anthropogenic La and Sm concentrations are predominantly present in the total fraction, which suggests that the anthropogenic La and Sm concentrations are associated with suspended matter. The anthropogenic La and Sm concentrations are lower in the suspended matter samples collected with the centrifuge, suggesting a bias of these La and Sm concentrations in the finer fraction of the suspended matter. The anthropogenic La en Sm concentrations remain relatively constant throughout the rivers, but close to Lake IJsselmeer and the North Sea, sedimentation causes a sharp decrease in the anthropogenic concentrations. Detailed sampling of sediments, suspended matter and water could give a

  13. Experimental study of REE, Ba, Sr, Mo and W partitioning between carbonatitic melt and aqueous fluid with implications for rare metal mineralization

    NASA Astrophysics Data System (ADS)

    Song, WenLei; Xu, Cheng; Veksler, Ilya V.; Kynicky, Jindrich

    2016-01-01

    Carbonatites host some unique ore deposits, especially rare earth elements (REE). Hydrothermal fluids have been proposed to play a significant role in the concentration and transport of REE and other rare metals in carbonatites, but experimental constraints on fluid-melt equilibria in carbonatitic systems are sparse. Here we present an experimental study of trace element (REE, Ba, Sr, Mo and W) partitioning between hydrous fluids and carbonatitic melts, bearing on potential hydrothermal activity associated with carbonatite ore-forming systems. The experiments were performed on mixtures of synthetic carbonate melts and aqueous fluids at 700-800 °C and 100-200 MPa using rapid-quench cold-seal pressure vessels and double-capsule assemblages with diamond traps for analyzing fluid precipitates in the outer capsule. Starting mixtures were composed of Ca, Mg and Na carbonates spiked with trace elements. Small amounts of F or Cl were added to some of the mixtures to study the effects of halogens on the element distribution. The results show that REE, Ba, Sr, Mo and W all preferentially partition into carbonatite melt and have fluid-melt distribution coefficients ( D f/m) below unity. The REE partitioning is slightly dependent on the major element (Ca, Mg and Na) composition of the starting mixtures, and it is influenced by temperature, pressure, and the presence of halogens. The fluid-melt D values of individual REE vary from 0.02 to 0.15 with D_{Lu}^{f} / {fm}{m} being larger than D_{La}^{f} / {fm}{m} by a factor of 1.1-2. The halogens F and Cl have strong and opposite effects on the REE partitioning. Fluid-melt D REE are about three times higher in F-bearing compositions and ten times lower in Cl-bearing compositions than in halogen-free systems. D_{W}^{f} / {fm}{m} and D_{Mo}^{f} / {fm}{m} are the highest among the studied elements and vary between 0.6 and 0.7; D_{Ba}^{f} / {fm}{m} is between 0.05 and 0.09, whereas D_{Sr}^{f} / {fm}{m} is at about 0.01-0.02. The

  14. Stability constants for mono- and dioxalato-complexes of Y and the REE, potentially important species in groundwaters and surface freshwaters

    NASA Astrophysics Data System (ADS)

    Schijf, J.; Byrne, R. H.

    2001-04-01

    We present the first measured set of stability constants for mono- and dioxalato-complexes of yttrium and all rare earths except Pm (Y+REE), Oxβ n = [MOx n3-2n] [M 3+] -1 [Ox 2-] -n(where [ ] ≡ concentrations, M ≡ Y+REE, and Ox 2- ≡ C 2O 42-). Aqueous solutions of Y+REE were titrated with oxalic acid in the presence of a cation-exchange resin, and Y+REE concentrations in the solution phase were measured by ICP-MS. This method allows investigation of all Y+REE simultaneously under identical conditions and is thus very sensitive to subtle inter-element variations in log Oxβ n. Experiments were performed at a single ionic strength ( I = 0.05 M), but at two values of pH. Patterns of log Oxβ 1 and log Oxβ 2, determined from our experiments, are similar in shape and reminiscent of those for carbonato-complexes. The average ratio of stepwise stability constants K 2/K 1 = Oxβ 2/( Oxβ 1) 2 is 0.05 ± 0.02 for Y+REE excluding La and Ce. Literature values of Oxβ 1(Eu) for 0.03 mol/L ≤ I ≤ 1 mol/L were used to derive the relation log Oxβ 1(Eu) = log Oxβ 10(Eu) - 6.132√ I/(1 + 1.47√ I) + 0.902 I, where log Oxβ 10(Eu) is the stability constant at infinite dilution. Applying this relation to all Y+REE, the following values of log Oxβ 10 (at zero ionic strength) were found: 6.66 (Y), 5.87 (La), 5.97 (Ce), 6.25 (Pr), 6.31 (Nd), 6.43 (Sm), 6.52 (Eu), 6.53 (Gd), 6.63 (Tb), 6.74 (Dy), 6.77 (Ho), 6.83 (Er), 6.89 (Tm), 6.95 (Yb), 6.96 (Lu). These values, which are based on direct measurements for each individual Y+REE, agree quite well with published extrapolations that are mostly based on linear free-energy relationships. Total oxalate concentrations of 10 -5-10 -3 M have been reported for soil solutions. Free oxalate ions persist at much lower pH than free carbonate ions and a simple speciation model demonstrates that oxalato-complexes can dominate Y+REE speciation in mildly acidic groundwaters of low-to-moderate alkalinity.

  15. Origin and history of the adcumulate eucrite, Moama as inferred from REE abundances, Sm-Nd and U-Pb systematics

    NASA Technical Reports Server (NTRS)

    Hamet, J.; Nakamura, N.; Unruh, D. M.; Tatsumoto, M.

    1978-01-01

    The abundances of Sm-Nd and U-Pb isotopes and of rare earth elements (REE) in Moama cumulate eucrite were investigated. The Sm-Nd data plotted on a Nd-143/Nd-144 vs Sm-147/Nd-144 evolution diagram define a line with a slope corresponding to an age of 4.58 plus or minus 0.05 billion years and an initial Nd-143/Nd-144 ratio of about 0.50684. Moama was found to contain the lowest overall trivalent REE abundances, the most light REE-depleted abundance pattern, and largest positive Eu anomaly of any eucrite yet studied. The REE data indicate that Moama could have been derived by about 1 to 5% fractional crystallization from a liquid with REE contents similar to Juvinas, or about 20 to 30% fractional crystallization from a Sioux County-like liquid. The data are consistent with the hypothesis that the Moama, Serra de Mage, and Moore county cumulate meteorites could have been derived from the same parent liquid. Results of the U-Th-Pb study indicate that the majority of the Pb in Moama is of terrestrial origin, and suggest that the meteorite has undergone a minor thermal event causing re-equilibration of the U-Pb system.

  16. Probing the neutrino mass through the cross correlation between the Rees-Sciama effect and weak lensing

    NASA Astrophysics Data System (ADS)

    Xu, Lixin

    2016-08-01

    Cosmology plays a fundamental role to determine the neutrino mass, therefore also to determine its mass hierarchy, since the massive neutrino contributes to the total matter density in the Universe at the background and perturbation levels, once it becomes non-relativistic. After the non-relativistic transition the fluctuations are smashed out at the scales k gg kfs. Therefore, the missing fluctuation in the total matter is imprinted on the large scale structure, say the suppression of the matter power spectrum ΔP/P ≈ ‑8fν at the scales k gg kfs. In this paper, instead of considering the linear perturbation theory, which is well understood in the presence of neutrino, we propose to use the cross correlation between the Rees-Sciama effect and weak lensing to probe the neutrino mass. At the small scales, the density contrast grows faster than the background scale factor δ ~ a, that makes a sign flipping on Φ' propto Script Hδ d ln (δ/a)/d ln a, which happens only in the non-linear regime. We show that the flipping scale in the cross power spectrum between the Rees-Sciama effect and weak lensing depends on the neutrino mass by assuming the shallow and deep weak lensing surveys. Our analysis shows that the Deep survey has larger signal-to-noise ratio S/N ~ 160. Finally, we use the Fisher information matrix to forecast constraint on the neutrino mass.

  17. Steep REE patterns and enriched Pb isotopes in southern Central American arc magmas: Evidence for forearc subduction erosion?

    NASA Astrophysics Data System (ADS)

    Goss, A. R.; Kay, S. M.

    2006-05-01

    The appearance of adakitic magmas with steep rare earth element (REE) patterns in southern Costa Rica and Panama at ˜4 Ma coincides with the collision of the Cocos Ridge and the inception of slab shallowing along the margin. Distinctly higher 206Pb/204Pb and 208Pb/204Pb ratios in these adakitic lavas than in older Miocene lavas suggest that components enriched in radiogenic Pb also entered the mantle magma source at ˜4 Ma. Published Pb-isotopic data for Central American arc lavas show that a similar radiogenic component is not present in lavas farther north and that maxima in post-Miocene 206Pb/204Pb and 208Pb/204Pb ratios occur in central Costa Rica and western Panama. Cretaceous and early Tertiary ophiolites in the forearc, whose origins have been linked to the Galápagos hot spot, show a similar spatial pattern in Pb isotopic ratios. The incorporation of ophiolitic forearc crust into the mantle wedge by forearc subduction erosion can explain the along-arc spatial and temporal pattern of Pb-isotopic ratios in southern Central American arc lavas. Partial melting of crust removed from the base of the forearc and subjected to high-pressure metamorphism in the subduction channel provides an explanation for the steep adakitic REE patterns in some Costa Rican and Panamanian arc lavas.

  18. Using Rare Earth Element (REE) tracers to identify preferential micro-sites of post-fire aeolian erosion

    NASA Astrophysics Data System (ADS)

    Van Pelt, R.; Zobeck, T. M.; Barnes, M. A.; Baddock, M.; D'Odorico, P.

    2011-12-01

    Plant communities in desert environments are spatially anisotropic. Nutrient islands develop below shrub canopies and in the bases of bunch grasses that enhance plant growth and reinforce the spatial anisotropy. Catastrophic disturbance that removes the vegetation such as fire or drought can result in the release of the trapped sediment which becomes redistributed over the landscape by wind and water. We applied Rare Earth Element (REE) tracers to different landscape positions of an anisotropic Northern Chihuahua Desert ecosystem at the Sevilleta National Wildlife Refuge in central New Mexico in an effort to study this process. We delineated three 0.5 m by 6 m plots of desert grassland and three plots of desert grassland-shrubland ecotone. Nitric acid was used to dissolve the REE oxides (Eu2O3, Dy2O3, and Pr6O11) which were then diluted in distilled water to a target concentration of 1 g REE l-1 and applied to the surface at a rate of 4 l m-2. From laboratory column studies using soil collected at the site, we estimated that this would penetrate the surface to a depth of 2.5 cm resulting in a sediment REE concentration of approximately 100 mg kg-1. Eu was applied to bare surfaces between vegetation characterized as sand with a surface covering of gravel, Pr was applied under grass clumps, and Dy was applied under Creosote Bush (Larrea tridentata (DC.). Two replicate 0.25 m2 areas of each surface type were also tagged to obtain a sample of tagged surface sediment for analysis. The area containing the plots was burned by U.S. Fish and Wildlife personnel on April 14, 2010. During the next two days, two grassland plots and two grassland-shrubland ecotone plots were tested by placing a portable boundary layer field wind tunnel over the plots and blowing them with 12 m s-1 wind for 10 minutes during which time a paired set of entrained sediment samples were captured at the outlet of the wind tunnel. This period was followed by a 30 minute test in which clean quartz sand

  19. Geochemical and Geochronologic Investigations of Zircon-hosted Melt Inclusions in Rhyolites from the Mesoproterozoic Pea Ridge IOA-REE Deposit, St. Francois Mountains, Missouri

    NASA Astrophysics Data System (ADS)

    Watts, K. E.; Mercer, C. N.; Vazquez, J. A.

    2015-12-01

    Silicic volcanic and plutonic rocks of an eroded Mesoproterozoic caldera complex were intruded and replaced by iron ore, and cross-cut by REE-enriched breccia pipes (~12% total REO) to form the Pea Ridge iron-oxide-apatite-REE (IOA-REE) deposit. Igneous activity, iron ore formation, and REE mineralization overlapped in space and time, however the source of REEs and other metals (Fe, Cu, Au) integral to these economically important deposits remains unclear. Melt inclusions (MI) hosted in refractory zircon phenocrysts are used to constrain magmatic components and processes in the formation of the Pea Ridge deposit. Homogenized (1.4 kbar, 1000°C, 1 hr) MI in zircons from rhyolites ~600 ft (PR-91) and ~1200 ft (PR-12) laterally from the ore body were analyzed for major elements by EPMA and volatiles and trace elements (H2O, S, F, Cl, REEs, Rb, Sr, Y, Zr, Nb, U, Th) by SHRIMP-RG. Metals (including Cu, Au) will be measured in an upcoming SHRIMP-RG session. U-Pb ages, Ti and REE were determined by SHRIMP-RG for a subset of zircon spots adjacent to MI (1458 ± 18 Ma (PR-12); 1480 ± 45 Ma (PR-91)). MI glasses range from fresh and homogeneous dacite-rhyolite (65-75 wt% SiO2) to heterogeneous, patchy mixtures of K-spar and quartz (PR-12, 91), and more rarely mica, albite and/or anorthoclase (PR-91). MI are commonly attached to monazite and xenotime, particularly along re-entrants and zircon rims (PR-91). Fresh dacite-rhyolite glasses (PR-12) have moderate H2O (~2-2.5 wt%), Rb/Sr ratios (~8) and U (~5-7 ppm), and negative (chondrite-normalized) Eu anomalies (Eu ~0.4-0.7 ppm) (typical of rhyolites), whereas HREEs (Tb, Ho, Tm) are elevated (~2-3 ppm). Patchy K-spar and quartz inclusions (PR-12, 91) have flat LREE patterns, and positive anomalies in Tb, Ho, and Tm. One K-spar inclusion (PR-91) has a ~5-50 fold increase in HREEs (Tb, Dy, Ho, Er, Tm) and U (35 ppm) relative to other MI. U-Pb and REE analyses of its zircon host are not unusual (1484 ± 21 Ma); its irregular shape

  20. Geochemical and Geochronologic Investigations of Zircon-hosted Melt Inclusions in Rhyolites from the Mesoproterozoic Pea Ridge IOA-REE Deposit, St. Francois Mountains, Missouri

    NASA Astrophysics Data System (ADS)

    Watts, K. E.; Mercer, C. N.; Vazquez, J. A.

    2014-12-01

    Silicic volcanic and plutonic rocks of an eroded Mesoproterozoic caldera complex were intruded and replaced by iron ore, and cross-cut by REE-enriched breccia pipes (~12% total REO) to form the Pea Ridge iron-oxide-apatite-REE (IOA-REE) deposit. Igneous activity, iron ore formation, and REE mineralization overlapped in space and time, however the source of REEs and other metals (Fe, Cu, Au) integral to these economically important deposits remains unclear. Melt inclusions (MI) hosted in refractory zircon phenocrysts are used to constrain magmatic components and processes in the formation of the Pea Ridge deposit. Homogenized (1.4 kbar, 1000°C, 1 hr) MI in zircons from rhyolites ~600 ft (PR-91) and ~1200 ft (PR-12) laterally from the ore body were analyzed for major elements by EPMA and volatiles and trace elements (H2O, S, F, Cl, REEs, Rb, Sr, Y, Zr, Nb, U, Th) by SHRIMP-RG. Metals (including Cu, Au) will be measured in an upcoming SHRIMP-RG session. U-Pb ages, Ti and REE were determined by SHRIMP-RG for a subset of zircon spots adjacent to MI (1458 ± 18 Ma (PR-12); 1480 ± 45 Ma (PR-91)). MI glasses range from fresh and homogeneous dacite-rhyolite (65-75 wt% SiO2) to heterogeneous, patchy mixtures of K-spar and quartz (PR-12, 91), and more rarely mica, albite and/or anorthoclase (PR-91). MI are commonly attached to monazite and xenotime, particularly along re-entrants and zircon rims (PR-91). Fresh dacite-rhyolite glasses (PR-12) have moderate H2O (~2-2.5 wt%), Rb/Sr ratios (~8) and U (~5-7 ppm), and negative (chondrite-normalized) Eu anomalies (Eu ~0.4-0.7 ppm) (typical of rhyolites), whereas HREEs (Tb, Ho, Tm) are elevated (~2-3 ppm). Patchy K-spar and quartz inclusions (PR-12, 91) have flat LREE patterns, and positive anomalies in Tb, Ho, and Tm. One K-spar inclusion (PR-91) has a ~5-50 fold increase in HREEs (Tb, Dy, Ho, Er, Tm) and U (35 ppm) relative to other MI. U-Pb and REE analyses of its zircon host are not unusual (1484 ± 21 Ma); its irregular shape

  1. Trace elements and REE fractionation in subsoils developed on sedimentary and volcanic rocks: case study of the Mt. Vulture area, southern Italy

    NASA Astrophysics Data System (ADS)

    Mongelli, Giovanni; Paternoster, Michele; Rizzo, Giovanna; Sinisi, Rosa

    2014-06-01

    There is an increasing interest in the distribution of rare earth elements (REEs) within soils, primarily as these elements can be used to identify pedogenetic processes and because soils may be future sources for REE extraction, despite much attention should be paid to the protection and preservation of present soils. Here, we evaluate the processes that control the distribution of REEs in subsoil horizons developed over differing lithologies in an area of low anthropogenic contamination, allowing estimates of the importance of source rocks and weathering. Specifically, this study presents new data on the distribution of REEs and other trace elements, including transition and high-field-strength elements, in subsoils developed on both Quaternary silica-undersaturated volcanic rocks and Pliocene siliciclastic sedimentary rocks within the Mt. Vulture area of the southern Apennines in Italy. The subsoils in the Mt. Vulture area formed during moderate weathering (as classified using the chemical index of alteration) and contain an assemblage of secondary minerals that is dominated by trioctahedral illite with minor vermiculite. The REEs, high-field-strength elements, and transition metals have higher abundances in subsoils that developed from volcanic rocks, and pedogenesis caused the Mt. Vulture subsoils to have REE concentrations that are an order of magnitude higher than typical values for the upper continental crust. This result indicates that the distribution of REEs in soils is a valuable tool for mineral exploration. A statistical analysis of inter-elemental relationships indicates that REEs are concentrated in clay-rich fractions that also contain significant amounts of low-solubility elements such as Zr and Th, regardless of the parent rock. This suggests that low-solubility refractory minerals, such as zircon, play a significant role in controlling the distribution of REEs in soils. The values of (La/Yb)N and (Gd/Yb)N fractionation indices are dependent on

  2. Distribution of REEs in box-core sediments offshore an industrial area in SE Sicily, Ionian Sea: evidence of anomalous sedimentary inputs.

    PubMed

    Di Leonardo, Rossella; Bellanca, Adriana; Neri, Rodolfo; Tranchida, Giorgio; Mazzola, Salvo

    2009-10-01

    The distribution of rare earth elements and yttrium (REEs+Y) has been investigated in box-core sediments recovered from four stations in the Sicilian coastal zone seawards of Augusta, one of the most industrialized and contaminated areas in the Mediterranean region. Shale-like REE patterns and low Y/Ho ratios (close to the chondritic ratio) suggest a dominant terrigenous (geogenic) source for REE. Slight enrichment of LREE over the HREE is interpreted as due to preferential adsorptive transfer of LREE from seawater to sediment particles. Samples from offshore cores exhibit slightly positive Gd and negative Ce anomalies. It is here hypothesized that main drivers of anthropogenic Gd flux towards the offshore are dredged contaminated materials that, recovered from the Augusta Bay, have been repeatedly discharged offshore. Consistent with the redox-chemistry of Ce, these anomalous sedimentary inputs induce a decrease of O(2) concentration in the sediment, which in turn triggers Ce regeneration. PMID:19735932

  3. Simple models for disequilibrium fractional melting and batch melting with application to REE fractionation in abyssal peridotites

    NASA Astrophysics Data System (ADS)

    Liang, Yan; Liu, Boda

    2016-01-01

    Disequilibrium melting arises when the kinetics of chemical exchange between a residual mineral and partial melt is sluggish compare to the rate of melting. To better understand the role of a finite crystal-melt exchange rate on trace element fractionation during mantle melting, we have developed a disequilibrium melting model for partial melting in an upwelling steady-state column. We use linear kinetics to approximate crystal-melt mass exchange rate and obtain simple analytical solutions for cases of perfect fractional melting and batch melting. A key parameter determining the extent of chemical disequilibrium during partial melting is an element specific dimensionless ratio (ε) defined as the melting rate relative to the solid-melt chemical exchange rate for the trace element of interest. In the case of diffusion in mineral limited chemical exchange, ε is inversely proportional to diffusivity of the element of interest. Disequilibrium melting is important for the trace element when ε is comparable to or greater than the bulk solid-melt partition coefficient for the trace element (k). The disequilibrium fractional melting model is reduced to the equilibrium perfect fractional melting model when ε is much smaller than k. Hence highly incompatible trace elements with smaller mobilities in minerals are more susceptible to disequilibrium melting than moderately incompatible and compatible trace elements. Effect of chemical disequilibrium is to hinder the extent of fractionation between residual solid and partial melt, making the residual solid less depleted and the accumulated melt more depleted in incompatible trace element abundances relative the case of equilibrium melting. Application of the disequilibrium fractional melting model to REE and Y abundances in clinopyroxene in abyssal peridotites from the Central Indian Ridge and the Vema Lithospheric Section, Mid-Atlantic Ridge revealed a positive correlation between the disequilibrium parameter ε and the

  4. The behaviour of REE and Zr-Hf fractionation in the volcanic waters of Nevado del Ruiz system (Colombia)

    NASA Astrophysics Data System (ADS)

    Inguaggiato, Claudio; Censi, Paolo; Zuddas, Pierpaolo; Makario Londoño, John; Chacón, Zoraida; Alzate, Diego; Brusca, Lorenzo; D'Alessandro, Walter

    2015-04-01

    The geochemical behaviour of Rare Earth Element (REE), Zr and Hf have been investigated in the thermal waters of Nevado del Ruiz volcanic system. These fluids are characterised by a wide range of pH ranging between 1.0 and 8.8. The acidic waters are sulphate dominated with different Cl/SO4 ratios. The Nevado del Ruiz waters allowed to investigate the behaviour of investigated elements in a wide spectrum of pH and chemical composition of water. The important role of the pH and the ionic complexes have been evidenced in the distribution of REE, Zr and Hf in the aqueous phase. The pH rules the precipitation of authigenic oxyhydroxides of Fe, Al producing changes in REE, Zr, Hf amount and strong anomalies of Cerium and Europium. Y-Ho and Zr-Hf (twin pairs) have different behaviour in strong acidic waters with respect to the water with higher pH. Yttrium and Ho have the same behaviour of Zr and Hf in waters with pH near neutral-to-neutral, showing super-chondritic ratios. The twin pairs showed to be sensitive to the co-precipitation and/or adsorption onto the surface of authigenic particulate suggesting an enhanced scavenging of Ho and Hf respect to Y and Zr, leading to super-chondritic ratios. In acidic waters a different behaviour of twin pairs occurs with chondritic Y/Ho ratios (reflecting the Y/Ho ratio of average local rock) and sub-chondritic Zr/Hf ratios. For the first time, Zr and Hf have been investigated in natural acidic fluids to understand the behaviour of these elements in extreme acidic conditions and different major anions chemistry. Zr/Hf molar ratio changes from 4.75 to 49.29 in water with pH<3.6. In strong acidic waters, a different fractionation of Zr and Hf have been recognised as function of major anion contents (Cl and SO4), suggesting the formation of complexes leading to sub-chondritic Zr/Hf molar ratios.

  5. Sorption of the Rare Earth Elements and Yttrium (REE-Y) in calcite: the mechanism of a new effective tool in identifying paleoearthquakes on carbonate faults

    NASA Astrophysics Data System (ADS)

    Moraetis, Daniel; Mouslopoulou, Vasiliki; Pratikakis, Alexandros

    2015-04-01

    A new tool for identifying paleoearthquakes on carbonate faults has been successfully tested on two carbonate faults in southern Europe (the Magnola Fault in Italy and the Spili Fault in Greece): the Rare Earth Element and Yttrium (REE-Y) method (Manighetti et al., 2010; Mouslopoulou et al., 2011). The method is based on the property of the calcite in limestone scarps to absorb the REE and Y from the soil during its residence beneath the ground surface (e.g. before its exhumation due to earthquakes). Although the method is established, the details of the enrichment mechanism are poorly investigated. Here we use published data together with new information from pot-experiments to shed light on the sorption mechanism and the time effectiveness of the REE-Y method. Data from the Magnola and Spili faults show that the average chemical enrichment is ~45%, in REE-Y while the denudation rate of the enriched zones is ~1% higher every 400 years due to exposure of the fault scarp in weathering. They also show that the chemical enrichment is significant even for short periods of residence time (e.g., ~100 years). To better understand the enrichment mechanism, we performed a series of pot experiments, where carbonate tiles extracted from the Spili Fault were buried into soil collected from the hanging-wall of the same fault. We irrigated the pots with artificial rain that equals 5 years of rainfall in Crete and at temperatures of 15oC and 25oC. Following, we performed sorption isotherm, kinetic and pH-edge tests for the europium (Eu), the cerium (Ce) and the ytterbium (Yt) that occur in the calcite minerals. The processes of adsorption and precipitation in the batch experiments are simulated by the Mineql software. The pot experiments indicate incorporation of the REE and Y into the surface of the carbonate tile which is in contact with the soil. The pH of the leached solution during the rain application range from 7.6 to 8.3. Nutrient release like Ca is higher in the leached

  6. Landslide-induced iron mobilisation shapes benthic accumulation of nutrients, trace metals and REE fractionation in an oligotrophic alpine stream

    NASA Astrophysics Data System (ADS)

    Johnston, Scott G.; Rose, Andrew L.; Burton, Edward D.; Webster-Brown, Jenny

    2015-01-01

    Large alpine landslides that entrain substantial organic material below the water table and create suspended floodplains may have long-term consequences for the mobilisation of redox sensitive elements, such as Fe, into streamwaters. In turn, the cycling of iron in aquatic systems can influence the fate of nutrients, alter primary productivity, enhance accumulation of trace metals and induce fractionation of rare earth elements (REE). In this study we examine a reach of a pristine oligotrophic alpine stream bracketing a 30 year-old landslide and explore the consequences of landslide-induced Fe mobilisation for aqueous geochemistry and the composition of benthic stream cobble biofilm. Elevated Fe2+ and Mn in landslide zone stream waters reflect inputs of circumneutral groundwater from the landslide debris-zone floodplain. Geochemical characteristics are consistent with reductive dissolution being a primary mechanism of Fe2+ and Mn mobilisation. Stream cobble biofilm in the landslide zone is significantly (P < 0.01) enriched in poorly crystalline Fe(III) (∼10-400 times background) and Mn (∼15-150 times background) (1 M HCl extractable; Fe(III)Ab). While the landslide zone accounts for less than ∼9% of the total stream length, we estimate it is responsible for approximately 60-80% of the stream's benthic biofilm load of poorly crystalline Fe(III) and Mn. Biofilm Fe(III) precipitates are comprised mainly of ferrihydrite, lepidocrocite and an organic-Fe species, while precipitate samples collected proximal to hyporheic seeps contain abundant sheath structures characteristic of the neutrophilic Fe(II)-oxidising bacteria Leptothrix spp. Stream-cobble Fe(III)-rich biofilm is accumulating PO43- (∼3-30 times background) and behaving as a preferential substrate for photosynthetic periphyton, with benthic PO43-, chlorophyll a, organic carbonHCl and total N all significantly positively correlated with Fe(III)Ab and significantly elevated within the landslide zone (P < 0

  7. Mixed-ligand complex compounds of rare-earth elements (REE) with acetylacetone and fumaric or maleic acid

    SciTech Connect

    Panyushkin, V.T.; Akhrimenko, N.V.

    1994-10-01

    Previously the authors investigated the possibility of synthesis of the f-block element mixed complexes with {beta}-diketones and organic unsaturated acids. The mixed-ligand complexes of lanthanides [Ln = Nd(III), Sm(III), Eu(III), Tb(III), Dy(III), Ho(III), and Yb(III)] with acetylacetone (acac) and fumaric or maleic acid (AcidH{sub 2}) were synthesized. The mixed-ligand complexes were prepared by the interaction of REE tris(acetylacetonates) [Ln(acac){sub 3}{center_dot} 3H{sub 2}O] with half as much excess of the organic acid in a solution of diethyl ether. According to the data of elemental analysis and thermogravimetric and spectroscopic investigations, the mixed complexes studied are of composition Ln(acac){sub 2}(AcidH){center_dot}H{sub 2}O.

  8. The Pasamonte unequilibrated eucrite: Pyroxene REE systematic and major-, minor-, and trace-element zoning. [Abstract only

    NASA Technical Reports Server (NTRS)

    Pun, A.; Papike, J. J.

    1994-01-01

    We are evaluating the trace-element concentrations in the pyroxenes of Pasamonte. Pasamonte is a characteristic member of the main group eucrites, and has recently been redescribed as a polymict eucrite. Our Pasamonte sample contained eucritic clasts with textures ranging from subophitic to moderately coarse-grained. This study concentrates on pyroxenes from an unequilibrated, coarse-grained eucrite clast. Major-, minor-, and trace-element analyses were measured for zoned pyroxenes in the eucritic clast of Pasamonte. The major- and minor-element zoning traverses were measured using the JEOL 733 electron probe with an Oxford-Link imaging/analysis system. Complemenatry trace elements were then measured for the core and rim of each of the grains by SIMS. The trace elements analyzed consisted of eight REE, Sr, Y, and Zr. These analyses were performed on a Cameca 4f ion probe. The results of the CI chondrite normalized (average CI trace-element analyses for several grains and the major- and minor-element zoning patterns from a single pyroxene grain are given. The Eu abundance in the cores of the pyroxenes represents the detection limit and therefore the (-Eu) anomaly is a minimum. Major- and minor-element patterns are typical for igneous zoning. Pyroxene cores are Mg enriched, whereas the rims are enriched in Fe and Ca. Also, Ti and Mn are found to increase, while Cr and Al generally decrease in core-to-rim traverses. The cores of the pyroxenes are more depleted in the Rare Earth Elements (REE) than the rims. Using the minor- and trace-element concentrations of bulk Pasamonte and the minor- and trace-element concentrations from the cores of the pyroxenes in Pasamonte measured in this study, we calculated partition coefficients between pyroxene and melt. This calculation assumes that bulk Pasamonte is representative of a melt composition.

  9. Nd isotopic composition and REE pattern in the surface waters of the eastern Indian Ocean and its adjacent seas

    SciTech Connect

    Amakawa, Hiroshi; Alibo, D.S.; Nozaki, Yoshiyuki

    2000-05-01

    The Nd isotopic composition and dissolved rare earth elements (REEs) have been measured in the surface waters along the 1996/97 R.V. Hakuho-Maru Expedition route from Tokyo to the Southern Ocean, southwest of Australia, through the Philippine and Indonesian Archipelago, the eastern Indian Ocean, the Bay of Bengal and the South China Sea. The radiogenic {epsilon}{sub Nd} values of {minus}1.3 and {minus}1.4 were found in the Sulu Sea and near the Lombok Strait, indicating the strong influence of surrounding volcanic islands, whereas non-radiogenic {epsilon}{sub Nd} values of less than {minus}10 were found in the Southern Ocean and the Bay of Bengal suggesting Nd of continental origin. The dissolved Nd concentrations also showed a wide range of variation from 2.8 to 19.6 pmol/kg and the trivalent REE patterns exhibited characteristic features that can be grouped into each different oceanic province. The geographical distribution of dissolved Nd is different from that of atmospherically derived {sup 210}Pb, but generally resembles that of coastally derived {sup 228}Ra. This strongly suggests that fluvial and coastal input predominates over eolian input for dissolved Nd in the surface ocean. However, the riverine dissolved Nd flux appears to be relatively minor, and remobilization of Nd from coastal and shelf sediments may play an important role in the total Nd input to the ocean. By modeling the distributions of the isotopic composition and concentration of Nd together with the activity ratio of {sup 228}Ra/{sup 226}Ra in the southeastern Indian Ocean, the authors estimate a mean residence time of Nd in the surface mixed layer to be 1.5--2.6 years. The short mean residence time is comparable with, or slightly longer than that of {sup 210}Pb suggesting similar chemical reactivity.

  10. Application of Markov Chain Monte Carlo Method to Mantle Melting: An Example from REE Abundances in Abyssal Peridotites

    NASA Astrophysics Data System (ADS)

    LIU, B.; Liang, Y.

    2015-12-01

    Markov chain Monte Carlo (MCMC) simulation is a powerful statistical method in solving inverse problems that arise from a wide range of applications, such as nuclear physics, computational biology, financial engineering, among others. In Earth sciences applications of MCMC are primarily in the field of geophysics [1]. The purpose of this study is to introduce MCMC to geochemical inverse problems related to trace element fractionation during concurrent melting, melt transport and melt-rock reaction in the mantle. MCMC method has several advantages over linearized least squares methods in inverting trace element patterns in basalts and mantle rocks. First, MCMC can handle equations that have no explicit analytical solutions which are required by linearized least squares methods for gradient calculation. Second, MCMC converges to global minimum while linearized least squares methods may be stuck at a local minimum or converge slowly due to nonlinearity. Furthermore, MCMC can provide insight into uncertainties of model parameters with non-normal trade-off. We use MCMC to invert for extent of melting, amount of trapped melt, and extent of chemical disequilibrium between the melt and residual solid from REE data in abyssal peridotites from Central Indian Ridge and Mid-Atlantic Ridge. In the first step, we conduct forward calculation of REE evolution with melting models in a reasonable model space. We then build up a chain of melting models according to Metropolis-Hastings algorithm to represent the probability of specific model. We show that chemical disequilibrium is likely to play an important role in fractionating LREE in residual peridotites. In the future, MCMC will be applied to more realistic but also more complicated melting models in which partition coefficients, diffusion coefficients, as well as melting and melt suction rates vary as functions of temperature, pressure and mineral compositions. [1]. Sambridge & Mosegarrd [2002] Rev. Geophys.

  11. Dust dispersal and Pb enrichment at the rare-metal Orlovka-Spokoinoe mining and ore processing site: insights from REE patterns and elemental ratios.

    PubMed

    Dolgopolova, Alla; Weiss, Dominik J; Seltmann, Reimar; Dulski, Peter

    2006-04-30

    Different geological, technogenic and environmental samples from the Orlovka-Spokoinoe Ta-Nb-Sn-W mining site and ore processing complex in Eastern Transbaikalia (Russia), were analysed for Pb, Y, Zr, Hf and rare earth elements (REE) to assess the effect of dust and metal dispersal on the environment within the Orlovka-Spokoinoe mining site. Potential source material analysed included ore-bearing and barren granites, host rocks, tailing pond sediments, and ore concentrates. Lichens and birch leaves were used as receptor samples. The REE enrichment relative to chondrite, the extent of the Eu anomalies, the enrichments of heavy REE (HREE), and Zr/Hf and Yb/Y ratios suggest that tailings, barren granites, and metasedimentary host rocks are the main sources of dust in the studied mining environment. In addition, calculated lead enrichment (relative to host rocks) suggests that the environment is polluted with Pb. Our results clearly demonstrate the potential of REE patterns and elemental ratios as a reliable technique to trace dust and metals sources and dispersal within a confined mining area offering a new tool for environmental assessment studies. PMID:16427193

  12. Does sediment geochemistry (based on selective extractions of Al and Fe and REE) provide a record of soil evolution?

    NASA Astrophysics Data System (ADS)

    Mourier, B.; Poulenard, J.; Blarquez, O.; Williamson, D.; Arnaud, F.; Carcaillet, C.

    2009-04-01

    Soil is a natural body occurring at the interface between the lithosphere, atmosphere and biosphere. As a result, the physical and chemical properties of soils evolve with time, and the reconstruction of their history represents a key to understand past environmental changes. Palaeolimnological techniques such as sediment geochemistry can be used to investigate changes in catchment history by providing information about soil development. However, due to the lack of conservative pedosignatures (soil proxies), only few paleoecological studies have attempted to reconstruct the history of soil genesis using geochemical analyses of lacustrine sediments. Here we present a multidisciplinary study which aims to use pedosignatures, defined by a previous soil study, in order to characterize the history of soil genesis, podzolization and chemical weathering processes in two sediment sequences. Moreover, we aim to compare the timing of soil evolution with other paleoenvironmental markers (macroremains, charcoals…) in order to infer the role of climate, vegetation and possible human activities as forcing factors. In a first step, the geochemical investigation of eight subalpine soil profiles from the inner Alps allowed to define relevant proxies of two major soil processes. Parent material normalized REE patterns provide a precise tracer of chemical weathering whereas the proportions of secondary Al- and Fe-bearing phases provide a tracer of the podzolisation process. Then, the same tracers were assessed on two lacustrine and peat sediment sequences (Loup and Thyl lakes) from the subalpine domain. The proxy records, spanning ca. 4.500 yr at the Thyl lake and ca. 13.500 yr at the Loup lake, indicate that both progressive and regressive pedogenesis occurred after the deglaciation. The Thyl record is highly contrasted: the progressive setting of the mixed cembra pine ecosystem is associated to the podzolisation process (secondary Al- and Fe-bearing phases are maximal) and the

  13. Karrat REE mineralization on Niaqornakavsak and extension on Umiamako Nuna, West Greenland: mineralogic, geochronologic, and carbon and oxygen isotope constraints on the origin

    NASA Astrophysics Data System (ADS)

    Mott, A.; Bird, D. K.; Grove, M.; Bernstein, S.; Mackay, H.; Rose, N.

    2011-12-01

    The Karrat rare earth element (REE) mineralization is located in the Niaqornakavsak (NIAQ) area of Qeqertarssuaq Island in Greenland (~72°N). A mineralized horizon occurs as a single distinct layer (35-40° dip) within an amphibolite host rock of the Qeqertarssuaq Formation: a member of the Paleoproterozoic Karrat Group sequence. Average Yttrium + REE-oxide (YREEO) concentration is ~1.0 wt. % with concentrations up to 2.59 wt. % over one meter intervals. Eight drill holes across three locations on NIAQ allow for an estimated true thickness of REE enrichment (YREEO ≥ 0.2 wt. %) of 29-38m in the east and central area, and a fault restricted thickness at the site in the west of 16m (at surface) to 28m (at depth). Two distinct metasomatic reaction zones comprise the mineralized horizon and are universal across NIAQ: the upper unit (CCA ~1.5 %YREEO) has a primary mineralogy of calcite + ankerite + fluorite (>50%), grunerite, cummingtonite, magnetite, fergusonite, bastnasite, allanite, and monazite, while the lower unit (BLC) consists of biotite (>50%), calcite, ilmenite, magnetite, allanite, fergusonite, and monazite. An extension of the Karrat REE deposit outcrops 7 km to the east on Umiamako Nuna. Hand samples from Umiamako Nuna similar to CCA (YREEO up to 2.4 wt. %) have been collected, but two exploratory drill holes revealed the majority of the REE enriched zone is comparable to the mineralogy of the incomplete reaction zone around CCA on NIAQ with concentrations of YREEO ranging from 0.5-1.0 wt. % with an estimated thickness of 15m. The mineralization consists of Ca-amphiboles, biotite, calcite, pyrite, albite, and garnet. Enrichment of REE continues to a depth of 60m from vein mineralization. In addition, a secondary occurrence at depth can be found on Umiamako Nuna tens of meters below the primary mineralized horizon, which is characterized by high modal concentrations of calcite, fluorite, and amphiboles. Carbon and oxygen isotope analyses of 145 carbonate

  14. Hydrothermal REE and Zr mobilization in the Strange Lake peralkaline granitic system: a reaction path model linked to petrological and geochemical observations

    NASA Astrophysics Data System (ADS)

    Gysi, A. P.; Williams-Jones, A. E.

    2013-12-01

    Extreme enrichment and hydrothermal mobilization of rare earth elements (REE) and other high-field strength elements (HFSE; i.e., Zr, Nb, Ta and Ti) is a feature of anorogenic alkaline and peralkaline igneous systems. Strange Lake in Quebec, Canada, is a mid-Proterozoic peralkaline granitic intrusion that is host to a world-class REE and HFSE deposit with >50 Mt of ore (>1.5 wt.% REE and >3 wt.% Zr). We have used Strange Lake as a natural laboratory and linked petrographic observations of the deposit and geochemical data with numerical simulations to constraint physicochemical conditions of hydrothermal REE and Zr mobilization and mineralization. The B-zone, in the NW of Strange Lake, contains a lens-shaped pegmatite-rich zone hosted in subsolvus granite. Three alteration styles were distinguished: i) an acid alteration caused by HCl-HF-bearing fluids from the pegmatites, ii) Na-metasomatism related to aegirinization/hematization of arfvedsonite, and iii) Ca-F-metasomatism involving late interaction of the rocks with a mixture of acidic F-rich and Ca-rich fluids. The acid alteration accounts for most of the hydrothermal mobilization of Zr and REE within and from the pegmatites, whereas the Ca-F-metasomatism is evident as late stage pore space fillings and veins of hydrothermal fluorite and quartz and a fluorite breccia. These different alteration styles are reflected in the bulk rock chemistry by variable mobility of Na, Fe, Al, Ca, F, HFSE and REE distinguishable on isocon diagrams. Elemental X-ray maps of REE- and Zr-minerals show evidence for a decoupled mobilization of LREE, HREE and Zr at different stages of fluid-rock interaction. Numerical simulations of the reaction of pegmatite with saline HF- and HCl-HF-bearing fluids at 400 °C to 250 °C predict the observed trends reasonably well. Fluids with pH <2 led to the formation of quartz and fluorite in the core of the pegmatites, and fluids with pH >4 to the formation of phyllosilicates and continued stability

  15. A Gradient in Cooling Rate Beneath the Moho at the Oman Ophiolite: Fresh Insights into Cooling Processes at Mid-Ocean Ridges from REE-Based Thermometry

    NASA Astrophysics Data System (ADS)

    Dygert, N. J.; Kelemen, P. B.; Liang, Y.

    2015-12-01

    The Wadi Tayin massif in the southern Oman ophiolite has a more than 10 km thick mantle section and is believed to have formed in a mid-ocean ridge like environment with an intermediate to fast spreading rate. Previously, [1] used major element geothermometers to investigate spatial variations in temperatures recorded in mantle peridotites and observed that samples near the paleo-Moho have higher closure temperatures than samples at the base of the mantle section. Motivated by these observations, we measured major and trace elements in orthopyroxene and clinopyroxene in peridotites from depths of ~1-8km beneath the Moho to determine closure temperatures of REE in the samples using the REE-in-two-pyroxene thermometer [2]. Clinopyroxene are depleted in LREE and have REE concentrations that vary depending on distance from the Moho. Samples nearer the Moho have lower REE concentrations than those deeper in the section (e.g., chondrite normalized Yb ranges from ~1.5 at the Moho to 4 at 8km depth), consistent with near fractional melting along a mantle adiabat. Orthopyroxene are highly depleted in LREE but measurements of middle to heavy REE have good reproducibility. We find that REE-in-two-pyroxene temperatures decrease with increasing distance from the Moho, ranging from 1325±10°C near the Moho to 1063±24°C near the base of the mantle section. Using methods from [3], we calculate cooling rates of >1000°C/Myr near the Moho, dropping to rates of <10°C/Myr at the bottom of the section. The faster cooling rate is inconsistent with conductive cooling models. Fast cooling of the mantle lithosphere could be facilitated by infiltration of seawater to or beneath the petrologic Moho. This can explain why abyssal peridotites from ultra-slow spreading centers (which lack a crustal section) have cooling rates comparable to those of Oman peridotites [3]. [1] Hanghøj et al. (2010), JPet 51(1-2), 201-227. [2] Liang et al. (2013), GCA 102, 246-260. [3] Dygert & Liang (2015

  16. Sedimentology of a glaciofluvial landsystem, Lough Ree area, Central Ireland: implications for ice margin characteristics during Devensian deglaciation

    NASA Astrophysics Data System (ADS)

    Delaney, Catherine

    2002-05-01

    Eskers in a glaciofluvial landsystem in the Lough Ree area, Central Ireland, exhibit two orientations. The most southerly esker in the area, the Athlone Esker, forms part of a dendritic esker system with paleocurrent directions indicating eastward drainage, while the Rooskagh Esker and associated eskers and kames immediately to the north were formed during southward drainage. Sediments indicate that sharp-crested, steep-sided sections of both ridges were formed within subglacial tunnels, while fan-shaped and flat-topped areas were formed as subaqueous outwash fans and deltas in standing water immediately in front of an ice-margin. The deposition of ice-marginal deposits indicating southward paleoflows against the side of the eastward flowing Athlone Esker indicates a 90° shift in the direction of ice surface slope, and a similar shift in the likely orientation of the ice margin. The absence of any evidence of intermediate ice- or water-flow directions indicates that the shift reflects a recession of ice, followed by a readvance from the north.

  17. Morphological and molecular characterisation of Ditrachybothridium macrocephalum Rees, 1959 (Cestoda: Diphyllidea) from Galeus melastomus Rafinesque in the Western Mediterranean.

    PubMed

    Dallarés, Sara; Pérez-Del-Olmo, Ana; Carrassón, Maite; Kuchta, Roman

    2015-09-01

    New morphological, molecular and ecological data for Ditrachybothridium macrocephalum Rees, 1959 (Cestoda: Diphyllidea) are presented and discussed based on specimens recovered from the blackmouth catshark Galeus melastomus Rafinesque (Scyliorhinidae) in the Western Mediterranean. A redescription of the plerocercus of this parasite is provided and new data on immature and mature worms including the first description of the eggs are reported, based on light and scanning electron microscopy observations. Analysis of 28S rDNA (domains D1-D3) sequences from plerocerci, immature and adult specimens revealed that they are conspecific with specimens from the North East Atlantic. Although previous authors considered that museum specimens identified as D. macrocephalum may represent more than one species, examination of type- and voucher material revealed no relevant morphological differences between museum specimens and the present material. Information on infection levels of D. macrocephalum is provided from a large number of host specimens (n = 170). This species was more abundant in juvenile than in adult hosts and on the middle slope than on the upper slope; this may be related to ontogenetic and bathymetric diet shifts of G. melastomus. PMID:26249521

  18. Composition of rare earth elements in settling particles collected in the highly productive North Pacific Ocean and Bering Sea: Implications for siliceous-matter dissolution kinetics and formation of two REE-enriched phases

    NASA Astrophysics Data System (ADS)

    Akagi, Tasuku; Fu, Feng-fu; Hongo, Yayoi; Takahashi, Kozo

    2011-09-01

    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

  19. Tracing thermal aquifers of El Chichón volcano-hydrothermal system (México) with 87Sr/ 86Sr, Ca/Sr and REE

    NASA Astrophysics Data System (ADS)

    Peiffer, L.; Taran, Y. A.; Lounejeva, E.; Solís-Pichardo, G.; Rouwet, D.; Bernard-Romero, R. A.

    2011-08-01

    The volcano-hydrothermal system of El Chichón volcano, Chiapas, Mexico, is characterized by numerous thermal manifestations including an acid lake, steam vents and boiling springs in the crater and acid and neutral hot springs and steaming ground on the flanks. Previous research on major element chemistry reveals that thermal waters of El Chichón can be divided in two groups: (1) neutral waters discharging in the crater and southern slopes of the volcano with chloride content ranging from 1500 to 2200 mg/l and (2) acid-to-neutral waters with Cl up to 12,000 mg/l discharging at the western slopes. Our work supports the concept that each group of waters is derived from a separate aquifer (Aq. 1 and Aq. 2). In this study we apply Sr isotopes, Ca/Sr ratios and REE abundances along with the major and trace element water chemistry in order to discriminate and characterize these two aquifers. Waters derived from Aq. 1 are characterized by 87Sr/ 86Sr ratios ranging from 0.70407 to 0.70419, while Sr concentrations range from 0.1 to 4 mg/l and Ca/Sr weight ratios from 90 to 180, close to average values for the erupted rocks. Waters derived from Aq. 2 have 87Sr/ 86Sr between 0.70531 and 0.70542, high Sr concentrations up to 80 mg/l, and Ca/Sr ratio of 17-28. Aquifer 1 is most probably shallow, composed of volcanic rocks and situated beneath the crater, within the volcano edifice. Aquifer 2 may be situated at greater depth in sedimentary rocks and by some way connected to the regional oil-gas field brines. The relative water output (l/s) from both aquifers can be estimated as Aq. 1/Aq. 2-30. Both aquifers are not distinguishable by their REE patterns. The total concentration of REE, however, strongly depends on the acidity. All neutral waters including high-salinity waters from Aq. 2 have very low total REE concentrations (< 0.6 μg/l) and are characterized by a depletion in LREE relative to El Chichón volcanic rock, while acid waters from the crater lake (Aq. 1) and acid

  20. Strong Input and Removal of Rare Earth Elements (REEs) Affect Dissolved Nd Isotope Composition of Seawater in the Panama Basin and the Eastern Equatorial Pacific

    NASA Astrophysics Data System (ADS)

    Frank, M.; Bosse, L. M.; Grasse, P.; Pahnke, K.; Hathorne, E. C.

    2014-12-01

    The distributions of dissolved REEs and Nd isotopes are controlled by inputs from land and water mass mixing. We present new data from the Panama Basin in the Eastern Equatorial Pacific (EEP) extending previous studies in the frame of the German SFB 754 project. The samples were taken following GEOTRACES protocols along a section from close to the Panamanian coast into the deep Panama Basin during FS Meteor cruise M90 in October/November 2012. Elevated Nd concentrations near 13 pmol/kg are found at the surface, which rapidly decrease to a subsurface minimum of 8 pmol/kg near 100m depth and then increase with water depth reaching maximum values of 18 pmol/kg at 3000 m water depth. However, these deep water concentrations are more than a factor of 2 lower than observed for North Pacific Deep Water (NPDW), which is the prevailing Pacific deep water mass at the sampling locations. All the REEs are depleted compared to NPDW suggesting that efficient uptake and scavenging dominate compared to release from remineralized particles. The surface waters show the most radiogenic Nd isotope values (ɛNd = +4.3) so far obtained globally. In combination with the Nd concentration maxima at the surface this suggests riverine dissolved and fine grained particulate inputs from southern Panama and Colombia where highly radiogenic volcanic rocks are exposed. Elevated ɛNd values above -1 in the entire water column are more radiogenic than in NPDW in the Central Pacific and in waters further south in the EEP, which confirms that release of REEs from the sinking volcanogenic material affects the entire water column. These data clearly document that significant inputs from land combined with efficient scavenging and removal in surface and deep waters control the distribution of REEs and Nd isotopes in the Panama Basin and the adjacent EEP (Grasse et al., 2012), which also has important implications for the distribution of other trace metals.

  1. Removal of high-salinity matrices through polymer-complexation-ultrafiltration for the detection of trace levels of REEs using inductively coupled plasma mass spectrometry.

    PubMed

    Duan, Hualing; Lin, Jijun; Gong, Zhenbin; Huang, Jiahua; Yang, Shifeng

    2015-10-01

    The polymer-complexation-ultrafiltration (PCUF) technique was applied to separate trace levels of rare earth elements (REEs), including scandium, yttrium and the lanthanides, from high-salinity matrices prior to their determination by inductively coupled plasma mass spectrometry (ICP-MS). The REEs were converted into REE-polymer complexes using the water-soluble polymer polyacrylic acid (PAA) at a specified pH, retained on the ultrafiltration membrane of centrifugal filter units, and finally eluted using diluted nitric acid to achieve separation from matrices with relatively high levels of various inorganic ions, such as sodium, potassium, calcium, magnesium, and chlorine ions. Numerous factors affecting the PCUF efficiency were optimized. The optimal conditions included the addition of 30 mg L(-1) of PAA, a pH of 7.5, a reaction time of 40 min at room temperature, and 5.0 mL of 3% nitric acid (v/v) eluent. Under these conditions, the analytes were quantitatively separated and recovered, with a resulting relative standard deviation (RSD) of less than 4.0% (0.05 µg L(-1), n=5) and standard addition recoveries between 89.2% (La) and 95.8% (Sm) for matrices of various salinities. The blank samples for the method ranged from 0.0003 µg L(-1) (Dy) to 0.0031 µg L(-1) (Sc), and the limits of quantification (LOQs, 10σ) were between 0.0006 µg L(-1) (Dy) and 0.0026 µg L(-1) (Sc). Furthermore, the salinity of the sample exhibited no effect on the REE-polymer complex formation process. Finally, the method was successfully applied for the determination of trace levels of dissolved Sc, Y, and lanthanides in coastal and estuarine seawater samples. PMID:26078161

  2. Deciphering human-climate interactions in ombrotrophic peat record : REE, Nd and Pb isotope signatures of dust supplies over the last 2500 years (Misten bog, Belgium)

    NASA Astrophysics Data System (ADS)

    Fagel, Nathalie; Allan, Mohamed; Le Roux, Gael; Mattielli, Nadine; Piotrowska, Natalia; Sikorski, Jarek

    2013-04-01

    A core of 173 cm of ombrotrophic Misten peat bog from the Hautes-Fagnes Plateau in Eastern Belgium provides a record of Rare Earth Elements (REE) deposition allowing to trace dust fluxes in West Europe during the historical record (last 2500 years). REE and lithogenic element analyses, as well as the Nd isotopes, were performed by HR-ICP-MS and MC-ICP-MS, respectively in peat layers dated by 210Pb and 14C. The parallel variations of REE concentration with lithogenic conservative elements confirms that REE are immobile in the studied peat bog and can be used as tracers of dust deposition. Dust fluxes show pronounced increase at BC300, AD600, 1000AD, 1200AD and from 1700AD, recording either influence of human activities (regional erosion due to forest clearing and soil cultivation activities) or local and regional climate changes. Using Nd isotope allows to decipher between local and distal causes. The ENd variability (-13 to -9) is interpreted by a mixing between dust sources from local soils and desert particles. Three periods characterised by dominant-distal sources (at 320AD, 1000 AD and 1700AD) are consistent with local wetter intervals as indicated by lower humification degree. Local erosion prevails durier drier (higher humification) intervals (-100AD, 600AD). On a global scale more distal supplies are driven during colder periods, in particular Oort and Maunder minima. Combining geochemical elementary content and isotope data in ombrotrophic peat allows to decipher between dust flux changes related to human and climate forcing.

  3. [Technique for removal of anaesthetic vapours from the operation theater. CO2-concentrations in the Jackson Rees system using a removal unit (author's transl)].

    PubMed

    Kroesen, G; Sankofi, P; Geir, W; Menardi, G

    1978-04-01

    The Jackson Rees system was used for short operations in 50 infants combined with or without a system for removal of excess anaesthetic vapours developed by the authors. The CO2-concentration in the system was measured directly before the upper airway of the patients. No statistically significance difference between the CO2-concentration with or without the use of the removal system. A variable power of suction up to 61/min is thought to be sufficient and harmless. PMID:655369

  4. Fluid-mediated alteration of (Y,REE,U,Th)-(Nb,Ta,Ti) oxide minerals in granitic pegmatite from the Evje-Iveland district, southern Norway

    NASA Astrophysics Data System (ADS)

    Duran, Charley J.; Seydoux-Guillaume, Anne-Magali; Bingen, Bernard; Gouy, Sophie; de Parseval, Philippe; Ingrin, Jannick; Guillaume, Damien

    2016-02-01

    We document the textural relations and chemical composition of (Y,REE,U,Th)-(Nb,Ta,Ti) oxide minerals in a granitic pegmatite from the Evje-Iveland district, southern Norway, using a combination of scanning and transmission electron microscopy, electron probe micro-analysis and infrared absorption spectroscopy. The (Y,REE,U,Th)-(Nb,Ta,Ti) oxide mineral is euxenite, which is strongly radiation damaged and surrounded by radial fractures. Within euxenite grains, three domains of distinct composition comprising unaltered, intermediate and altered euxenite, have been identified. In most cases pyrochlore occurs as corroded grain boundaries around euxenite and within relict fractures. Intermediate and altered euxenite are depleted in U, Pb, Ti, Nb, and Y, but enriched in Si and Ca relative to unaltered euxenite. Pyrochlore is also enriched in Fe, Pb, Zr and LREE relative to all euxenite phases. Altered domains of euxenite have deficient analytical totals and contain O-H. These domains are metamict and contain nanopores and nanodomains enriched in U and Ca. We suggest that as radiation damage accumulated in euxenite, radial fractures developed around the euxenite grains, thus allowing fluid infiltration. In the presence of fluid, euxenite was replaced by secondary euxenite then pyrochlore, owing to dissolution-precipitation and diffusion reactions. During alteration, U and the strategic metals Nb, Ti, and REE were mobilized at both the nanoscale and the scale of the pegmatite.

  5. Enrichment of Rare Earth and Niobium from a REE-Nb-Fe Associated Ore via Reductive Roasting Followed by Magnetic Separation

    NASA Astrophysics Data System (ADS)

    Liu, Mudan; You, Zhixiong; Peng, Zhiwei; Li, Xiang; Li, Guanghui

    2016-02-01

    REE-Nb-Fe ore is a typical refractory resource rich in valuable elements. In this article, coal-based reductive roasting followed by magnetic separation is proposed to recover rare earth element (REE), niobium (Nb), and powdered metallic iron (Fe) concentrate from a REE-Nb-Fe raw concentrate containing 31.9% total iron grade (TFe), 3.2% rare earth oxides (REO), and 2.9% Nb2O5. Sodium sulfate is employed to enhance the reduction of iron oxide and to facilitate the growth of metallic iron grains. A magnetic fraction with TFe of 89.3%, iron metallization of 95.8% and iron recovery of 91.5% is obtained by magnetic separation after the raw concentrate is reduced to 1100°C for 120 min in the presence of 15 wt.% sodium sulfate. The contents of rare earth and niobium in the nonmagnetic fraction are enriched to 5.4% (REO) and 4.6% (Nb2O5) with recoveries of 96.1% and 95.8%, respectively. The TFe in the nonmagnetic fraction obtained after the separation is decreased to 4.8% accordingly. The reactions between sodium sulfate and SiO2/Al2O3 enhance the reduction by destroying the mineral structure. The separation of iron from rare earth and niobium is highly improved as metallic iron grains grow markedly when roasted in the presence of sodium sulfate.

  6. Petrography and Geochemistry (Trace, Ree and Pge) of Pedda Cherlo Palle Gabbro-Diorite Pluton, Prakasam Igneous Province, Andhra Pradesh, India

    NASA Astrophysics Data System (ADS)

    Subramanyam, K. S. V.; Reddy, U. V. B.; Balaram, V.; Roy, Parijat

    2015-09-01

    Prakasam Igneous Province (PIP) is an important geological domain in the Eastern Dharwar Craton (EDC), found in the junction zone between the EDC and Eastern Ghat Mobile Belt (EGMB). The Pedda Cherlo Palle (PCP) gabbros are massive, leucocratic-mesocractic, and show cumulus textures with minerals plagioclase, cpx, and amphiboles. Compositionally, plagioclase is a labradorite-bytownite, cpx is diopside to augite, olivines are hyalosiderites and amphiboles are magnesiohornblendes. PCP gabbros have normal SiO2, high Al2O3, moderate to high TiO2, Na2O and medium Fe2O3, so, classified as subalkaline tholeiitic gabbros. Fractionated rare earth element (REE) patterns, high abundance of large ion lithofile elements (LILE) and transitional metals coupled with light REE (LREE) relative enrichment over heavy REE (HREE) and Nb are characteristics of partial melting of depleted mantle and melts that have undergone fractional crystalisation. These partial melts are enriched in LREE and LILE, due to the addition of slab derived sediment and fluids. PCP gabbros contain low abundance (5.1 to 24.6 ng/g) of platinum group elements (PGE), and show an increase in the order Ir>Os>Pt>Ru»Pd>Rh. We propose that the subduction related intraoceanic island arc might have accreted to the southeastern margin of India to the east of Cuddapah basin in a collisional regime that took place during Ur to Rodinia amalgamations.

  7. Dynamics of REE accumulation and fractionation in the subcolloidal fraction of bottom sediments in the Razdol'naya River-Amur Bay section, Sea of Japan

    NASA Astrophysics Data System (ADS)

    Polyakov, D. M.

    2016-05-01

    The REE contents (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu) are determined by atomic emission spectroscopy in the subcolloidal fraction of bottom sediments in the Razdol'naya River-Amur Bay section. The mean contents of lanthanides in soils and river bottom sediments (before the mixing zone) are calculated. The increase in REE content and the fractioning in the series from light to middle and heavy REE in sediments of different estuary zones (river, water mixing, and marine), with the latter related to flocculation, sorption on iron and manganese hydroxides, clay minerals (hydromica, smectites), and lifetime accumulation of marine plankton, are dtermined. Via extraction of 0.5 N sodium hydroxide solution, the content of lanthanides associated with humic substances of subcolloidal fraction from the Amur Bay sediments are determined: 1.3 to 8.2% of La; 1.1 to 11% of Ce; and 0.3 to 1.5 of Gd.

  8. REE variation in alkaline mafic lavas across the North Tanzanian Divergence zone, a possible indicator of varying lithospheric thickness

    NASA Astrophysics Data System (ADS)

    Mana, S.; Carr, M. J.; Feigenson, M.; Furman, T.; Swisher, C. C.

    2012-12-01

    systematic REE variations (Sm/Yb versus La/Sm) that are consistent with different degrees of partial melting (La/Sm), and varying amounts of garnet and amphibole in the source (Sm/Yb). Many of the more evolved samples have greater radiogenic isotopic ratios and evolve via assimilation and fractional crystallization to lower Sm/Yb and higher La/Sm. Different degree of partial melting may reflect heat flow variations, while heterogeneity in the source is consistent with pressure conditions that imply changes in the depth of melting. In fact, REE abundances of key NTD volcanics (e.g. Essimingor) indicate melting in the garnet and phlogopite stability zone indicating the presence of a relatively thick lithosphere, while the absence of garnet indicate areas characterized by thinning of the lithosphere. MacIntyre, R.M., Mitchell, J.G., Dawson, J.B., 1974. Age of fault movements in Tanzanian sector of East African Rift System. Nature 247, 354-356.

  9. Origin of the Rubian carbonate-hosted magnesite deposit, Galicia, NW Spain: mineralogical, REE, fluid inclusion and isotope evidence

    NASA Astrophysics Data System (ADS)

    Kilias, Stephanos P.; Pozo, Manuel; Bustillo, Manuel; Stamatakis, Michael G.; Calvo, José P.

    2006-10-01

    The Rubian magnesite deposit (West Asturian—Leonese Zone, Iberian Variscan belt) is hosted by a 100-m-thick folded and metamorphosed Lower Cambrian carbonate/siliciclastic metasedimentary sequence—the Cándana Limestone Formation. It comprises upper (20-m thickness) and lower (17-m thickness) lens-shaped ore bodies separated by 55 m of slates and micaceous schists. The main (lower) magnesite ore body comprises a package of magnesite beds with dolomite-rich intercalations, sandwiched between slates and micaceous schists. In the upper ore body, the magnesite beds are thinner (centimetre scale mainly) and occur between slate beds. Mafic dolerite dykes intrude the mineralisation. The mineralisation passes eastwards into sequence of bedded dolostone (Buxan) and laminated to banded calcitic marble (Mao). These show significant Variscan extensional shearing or fold-related deformation, whereas neither Rubian dolomite nor magnesite show evidence of tectonic disturbance. This suggests that the dolomitisation and magnesite formation postdate the main Variscan deformation. In addition, the morphology of magnesite crystals and primary fluid inclusions indicate that magnesite is a neoformed hydrothermal mineral. Magnesite contains irregularly distributed dolomite inclusions (<50 μm) and these are interpreted as relics of a metasomatically replaced dolostone precursor. The total rare earth element (REE) contents of magnesite are very similar to those of Buxan dolostone but are depleted in light rare earth elements (LREE); heavy rare earth element concentrations are comparable. However, magnesite REE chondrite normalised profiles lack any characteristic anomaly indicative of marine environment. Compared with Mao calcite, magnesite is distinct in terms of both REE concentrations and patterns. Fluid inclusion studies show that the mineralising fluids were MgCl2-NaCl-CaCl2-H2O aqueous brines exhibiting highly variable salinities (3.3 to 29.5 wt.% salts). This may be the result

  10. A possible difference in cooling rates recorded in REE in coexisting pyroxenes in peridotites from supra-subduction ophiolites and mid-ocean ridges

    NASA Astrophysics Data System (ADS)

    Dygert, N. J.; Liang, Y.; Kelley, K. A.

    2013-12-01

    Recently a REE-in-two-pyroxene thermometer was developed for mafic and ultramafic rocks [1]. This new thermometer is based on temperature sensitive REE partition coefficients between coexisting pyroxenes and calibrated against laboratory partitioning data. Because REE diffusion rates in pyroxene are relatively slow, the thermometer reads a higher temperature than major element based pyroxene thermometers. The difference between major and trace element derived temperatures depends primarily on cooling rate. Here we report new trace element data for peridotites from Trinity and Josephine ophiolites and a modern supra-subduction zone (SSZ) ophiolite analogue (the Mariana trench) determined by laser ablation ICP-MS. We inverted temperatures from the new data and globally distributed ophiolitic peridotite from eight literature studies (Figure 1). Data quality was carefully monitored leaving temperatures from 65 samples. Individual ophiolites usually have temperatures clustered within a range of a few hundred degrees, but the temperature range for the global dataset is greater than 700°C (688-1401°C). Temperatures calculated for the same samples using the two pyroxene thermometer of Brey and Köhler [2] are considerably lower (564-1049°C). REE temperatures are plotted against the major element temperatures [2] in Figure 1. Abyssal peridotites reported in [1] are shown by the peach field. Much of the ophiolite data plots farther from the blue 1:1 line than the abyssal peridotites, suggesting SSZ lithospheric mantle may cool more rapidly at those ophiolites. Fast cooling can be attributed to one or more dynamic differences between mid-ocean ridge (MOR) environments and supra-subduction environments, such as enhanced hydrothermal circulation, thinner oceanic crust, or rapid cooling due to basin closure and obduction. We note that several ophiolites appear to cool more slowly than the abyssal peridotites, however in those samples geochemical evidence suggests secondary

  11. Origin and evolution of the Nakhla meteorite inferred from the Sm-Nd and U-Pb systematics and REE, Ba, Sr, Rb and K abundances

    USGS Publications Warehouse

    Nakamura, N.; Unruh, D.M.; Tatsumoto, M.; Hutchison, R.

    1982-01-01

    Analyses of Sm-Nd and U-Th-Pb systematics, REE, Ba, Sr, Rb and K concentrations were carried out for whole rock and mineral separates from the Nakhla meteorite. The 1.26 ??.07 b.y. Sm-Nd age obtained in this work is in good agreement with those previously obtained by the Rb-Sr and Ar-Ar methods. The high initial ??{lunate}Nd value of +16 suggests that Nakhla was derived from a light REE-depleted, old planetary mantle source. U-Th-Pb data, after correction for pre-analytical terrestrial Pb contamination assuming an age of 1.26 b.y., suggest that the age of the Nakhla source is ???4.33 b.y. The agreement in the age determined by three independent radiometric methods and the high initial ??{lunate}Nd value strongly suggest that the 1.3 b.y. age dates one thorough igneous event in the parent body which not only reset these isotopic systems but also established the chemical and petrologic characteristics observed for the Nakhla meteorite. Using a three-stage Sm-Nd evolution model in combination with LIL element data and estimated partition coefficients, we have tested partial melting and fractional crystallization models to estimate LIL element abundances in a possible Nakhla source. Our model calculations suggest that partial melting of the light REE-depleted source followed by extensive fractional crystallization (???50%) of the partial melt could account for the REE abundances in the Nakhla constituent minerals. The estimated source is depleted in the light REE, Ba, Rb and K and therefore may resemble the MORB source in the earth's upper mantle or the upper 60-300 km of the moon. The significantly younger age of Nakhla than the youngest lunar rock; the young differentiation age inferred from the U-Th-Pb data, and the estimated LIL element abundances (including those of K, U and Th) in the source suggest that the Nakhla meteorite may have been derived from a relatively large, well-differentiated planetary body such as Mars. ?? 1982.

  12. Geochemistry of Lower Cretaceous limestones of the Alisitos Formation, Baja California, México: Implications for REE source and paleo-redox conditions

    NASA Astrophysics Data System (ADS)

    Madhavaraju, J.; Löser, Hannes; Lee, Yong Il; Santacruz, R. Lozano; Pi-Puig, T.

    2016-03-01

    Measurement of the major and trace elements were carried out on the Lower Cretaceous limestones interbedded in the volcano-sedimentary Alisitos Formation, northwestern México to understand the source of rare earth elements (REEs) and paleo-redox conditions. The five limestone beds (from the base up, Unit 5 to Unit 9) of the Alisitos Formation show large variations in SiO2 content (0.9-27.9%). A low concentration of CaO is observed in Unit 6 and Unit 8, and high content of CaO is observed in Unit 5, Unit 7 and Unit 9. The limestones are depleted in many trace elements with respect to Post-Archaean Australian Shale (PAAS), whereas Sr shows slight enrichment when compared to PAAS. The concentrations of ΣREE are higher in Unit 6 and Unit 8 (37.4 ± 7.5; 46.6 ± 19.4; respectively) than Unit5, Unit7, and Unit 9 (9.1 ± 3.2; 11.3 ± 9.4; 4.2 ± 2.5; respectively). The limestones of the Alisitos Formation show a non-seawater-like REE + Y pattern with positive Eu anomalies relative to PAAS (0.95-2.47). Variations in ΣREE, Al2O3, Zr, Sc, REE + Y patterns, and Y/Ho ratios are influenced mainly by the amount of terrigenous materials. The variations in the Eu/Eu*, La/Sc and La/Co suggest that the terrigenous materials included in the lower four limestone beds (from Unit 5, Unit 6, Unit 7 and Unit 8) were likely contributed by intermediate to felsic rocks whereas terrigenous materials from Unit 9 were derived from mafic to intermediate source rocks. The slightly negative to slightly positive Ce anomalies in the studied limestones resulted from variations in the bottom water oxygenation. This was also corroborated by V/Cr and Ni/Co ratios suggesting that the depositional environments experienced large fluctuations in oxygenation conditions ranging from oxic to anoxic conditions during the deposition of limestones of the Alisitos Formation.

  13. Sedimentary carbonate-hosted giant Bayan Obo REE-Fe-Nb ore deposit of Inner Mongolia, China; a cornerstone example for giant polymetallic ore deposits of hydrothermal origin

    USGS Publications Warehouse

    Chao, E.C.T.; Back, J.M.; Minkin, J.A.; Tatsumoto, M.; Junwen, Wang; Conrad, J.E.; McKee, E.H.; Zonglin, Hou; Qingrun, Meng; Shengguang, Huang

    1997-01-01

    Detailed, integrative field and laboratory studies of the textures, structures, chemical characteristics, and isotopically determined ages and signatures of mineralization of the Bayan Obo deposit provided evidence for the origin and characteristics favorable for its formation and parameters necessary for defining giant polymetallic deposits of hydrothermal origin. Bayan Obo is an epigenetic, metasomatic, hydrothermal rare earth element (REE)-Fe-Nb ore deposit that is hosted in the metasedimentary H8 dolostone marble of the Middle Proterozoic Bayan Obo Group. The metasedimentary sequence was deposited on the northern continental slope of the North China craton. The mine area is about 100 km south of the suture marking Caledonian subduction of the Mongolian oceanic plate from the north beneath the North China craton. The mineralogy of the deposit is very complex, consisting of more than 120 different minerals, some of which are epigenetic minerals introduced by hydrothermal solutions, and some of which are primary and secondary metamorphic minerals. The major REE minerals are monazite and bastnaesite, whereas magnetite and hematite are the dominant Fe-ore minerals, and columbite is the most abundant Nb mineral. Dolomite, alkali amphibole, fluorite, barite, aegirine augite, apatite, phlogopite, albite, and microcline are the most widespread gangue minerals. Three general types of ores occur at Bayan Obo: disseminated, banded, and massive ores. Broad zoning of these ore types occurs in the Main and East Orebodies. Disseminated ores are in the outermost zone, banded ores are in the intermediate zone, and massive ores are in the cores of the orebodies. On the basis of field relations, host rocks, textures, structures, and mineral assemblages, many varieties of these three types of ores have been recognized and mapped. Isotopic dating of monazite, bastnaesite, aeschynite, and metamorphic and metasomatic alkali amphiboles associated with the deposit provides constraints

  14. Large sedimentary aquifer systems functioning. Constraints by classical isotopic and chemical tools, and REE in the Eocene sand aquifer, SW France

    NASA Astrophysics Data System (ADS)

    Petelet-Giraud, E.; Negrel, P. J.; Millot, R.; Guerrot, C.; Brenot, A.; Malcuit, E.

    2010-12-01

    continuous decrease of water levels in the IMS aquifer for instance constitute major indicators to be taken into account for water management at the aquifer system scale. Major elements variability was interpreted in terms of water-rock interactions in these confined systems isolated from anthropogenic influence, with the main role played by evaporites on the water salinity (up to 2.5 g.L-1). Rare Earth Elements (REE) were also analysed in some groundwater samples, resulting in a large variability of UCC normalized-REE patterns, ΣREE ranging from 1.9 to 50.6 µg.L-1, with no dependence on TDS. For instance, interaction with carbonates delivers REE flat patterns and highest ΣREE. The REE patterns and control by key parameters are investigated in order to test REE as a potential supplementary geochemical tracer to recognize the aquifer type hosting groundwater.

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

    NASA Astrophysics Data System (ADS)

    Friend, C. R. L.; Nutman, A. P.; Bennett, V. C.; Norman, M. D.

    2008-02-01

    Modern chemical sediments display a distinctive rare earth element + yttrium (REE + Y) pattern involving depleted LREE, positive La/La*SN, Eu/Eu*SN, and YSN 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

  16. Fluid-driven destabilization of REE-bearing accessory minerals in the granitic orthogneisses of North Veporic basement (Western Carpathians, Slovakia)

    NASA Astrophysics Data System (ADS)

    Ondrejka, M.; Putiš, M.; Uher, P.; Schmiedt, I.; Pukančík, L.; Konečný, P.

    2016-02-01

    A variety of rare earth elements-bearing (REE) accessory mineral breakdowns were identified in granitic orthogneisses from the pre-Alpine basement in the Veporic Unit, Central Western Carpathians, Slovakia. The Ordovician granitic rocks were subjected to Variscan metamorphic-anatectic overprint in amphibolite facies. Chemical U-Th-Pb dating of monazite-(Ce) and xenotime-(Y) reveal their primary magmatic Lower to Middle Ordovician age (monazite: 472 ± 4 to 468 ± 6 Ma and xenotime: 471 ± 13 Ma) and/or metamorphic-anatectic Variscan (Carboniferous, Visean) age (monazite: 345 ± 3 Ma). Younger fluid-rock interactions caused breakdown of primary magmatic and/or metamorphic-anatectic monazite-(Ce), xenotime-(Y), fluorapatite and allanite-(Ce). Fluid-induced breakdown of xenotime-(Y) produced numerous tiny uraninite inclusions within the altered xenotime-(Y) domains. The monazite-(Ce) breakdown produced secondary egg-shaped coronal structures of different stages with well-developed concentric mineral zones. Secondary sulphatian monazite-(Ce) (up to 0.15 apfu S) occasionally formed along fluorapatite fissures. Localized fluorapatite and monazite-(Ce) recrystallization resulted in a very fine-grained, non-stoichiometric mixture of REE-Y-Fe-Th-Ca-P-Si phases. Finally, allanite-(Ce) decomposed to secondary REE carbonate minerals (members of the bastnäsite and synchysite groups) and calcite in some places. Although the xenotime alteration and formation of uraninite inclusions is believed to be the result of dissolution-reprecipitation between early magmatic xenotime and late-magmatic granitic fluids, the monazite, apatite and allanite breakdowns were driven by metamorphic hydrothermal fluids. While earlier impact of post-magmatic fluids originated probably from Permian acidic volcanic and microgranitic veins crosscutting the orthogneisses, another fluid-rock interaction event most likely occurred during Late Cretaceous metamorphism in the Veporic basement and covering

  17. Volatile-induced transport of HFSE, REE, Th and U in arc magmas: evidence from zirconolite-bearing vesicles in potassic lavas of Lewotolo volcano (Indonesia)

    NASA Astrophysics Data System (ADS)

    de Hoog, Jan C. M.; van Bergen, Manfred J.

    Potassium-rich calc-alkaline lavas of Lewotolo volcano, situated in the East Sunda Arc, Indonesia, contain the rare mineral zirconolite (CaZrTi2O7). Samples in which tiny grains of this mineral (3-25μm in size) were found span the entire range of lava compositions (47-62wt% SiO2). To the best of our knowledge, this is the first record of primary zirconolite in juvenile arc volcanics. The mineral forms part of a vesicle-filling assemblage consisting of a network of quenched feldspar crystals and an SiO2 phase, probably cristobalite. High contents of Th, U and REE (up to 9.3, 4.3 and 15.6wt% oxide respectively) and very high Fe contents (up to 13.5wt% Fe2O3) distinguish these zirconolites from those of other rock types. The extraction of volatile-rich phases with changing compositions in successive stages is considered to be responsible for the zirconolite formation. We hypothesise that a fluid capable of transporting HFSE, REE, Th and U was extracted from the magma and (partly) crystallised within voids which had formed earlier upon saturation of an aqueous fluid. Assuming that zirconolite compositions largely reflect trace metal contents of the coexisting fluid phase, significant amounts of `immobile' elements must have been transported on a macroscopic scale. Our findings thus point to a late-stage transfer of HFSE, REE, Th and U between different domains in a cooling magma body. Such a volatile-induced redistribution of trace elements at shallow levels of high-K volcanic systems may be significant for conventional geochemical modelling of magma evolution and for Th-U disequilibrium studies.

  18. A precise 232Th-208Pb chronology of fine-grained monazite: Age of the Bayan Obo REE-Fe-Nb ore deposit, China

    USGS Publications Warehouse

    Wang, Jingyuan; Tatsumoto, M.; Li, X.; Premo, W.R.; Chao, E.C.T.

    1994-01-01

    We have obtained precise Th-Pb internal isochron ages on monazite and bastnaesite for the world's largest known rare earth elements (REE)-Fe-Nb ore deposit, the Bayan Obo of Inner Mongolia, China. The monazite samples, collected from the carbonate-hosted ore zone, contain extremely small amounts of uranium (less than 10 ppm) but up to 0.7% ThO2. Previous estimates of the age of mineralization ranged from 1.8 to 0.255 Ga. Magnetic fractions of monazite and bastnaesite samples (<60-??m size) showed large ranges in 232Th 204Pb values (900-400,000) and provided precise Th-Pb internal isochron ages for paragenetic monazite mineralization ranging from 555 to 398 Ma within a few percent error (0.8% for two samples). These results are the first indication that REE mineralization within the giant Bayan Obo ore deposit occurred over a long period of time. The initial lead isotopic compositions (low 206Pb 204Pb and high 208Pb 204Pb) and large negative ??{lunate}Nd values for Bayan Obo ore minerals indicate that the main source(s) for the ores was the lower crust which was depleted in uranium, but enriched in thorium and light rare earth elements for a long period of time. Zircon from a quartz monzonite, located 50 km south of the ore complex and thought to be related to Caledonian subduction, gave an age of 451 Ma, within the range of monazite ages. Textural relations together with the mineral ages favor an epigenetic rather than a syngenetic origin for the orebodies. REE mineralization started around 555 Ma (disseminated monazite in the West, the Main, and south of the East Orebody), but the main mineralization (banded ores) was related to the Caledonian subduction event ca. 474-400 Ma. ?? 1994.

  19. Mesozoic-Cenozoic thermal evolution of lithospheric mantle beneath the North China Craton: evidence from REE-in-two-pyroxene temperatures of mantle xenoliths

    NASA Astrophysics Data System (ADS)

    Wang, C.; Xu, W.; Liang, Y.

    2014-12-01

    Thermal state is an important property for us to understand the nature of the lithospheric mantle beneath the North China Craton (NCC). Traditionally, it was obtained by calculating equilibrium temperatures for the mantle xenoliths using thermometers based on major element compositions of coexisting minerals. A REE-in-two-pyroxene thermometer developed by Liang et al. (2013) is able to extract near-solidus temperatures,which can deduce the thermal histories of mantle rocks in combination with major-element-in-two-pyroxene temperatures (Tmaj). We calculated REE temperatures (TREE) for mantle samples from the NCC including ancient refractory peridotites entrained by Early Cretaceous high-Mg diorites from the central NCC (Fushan), Mantle pyroxenites entrained by Early Cretaceous basalts from the eastern NCC (Feixian and Fangcheng), and fertile/moderately depleted peridotites entrained by <100 Ma basalts from the central and eastern NCC. The Fushan peridotites have low Tmaj (<880°C) and mismatched high TREE (780-1150°C), indicating that the ancient mantle was subjected to melt-rock reactions. The Feixian and Fangcheng pyroxenites have both high Tmaj (>890°C) and high TREE - Tmaj values (80-220°C), suggestive of a hot and fast-cooled mantle in Early Cretaceous. The peridotites in <100 Ma basalts have similar TREE and Tmaj, characteristics of well-equilibrated mantle. Based on the thermometric data, we suggest that the transition of nature of the NCC lithospheric mantle is marked by the interaction between ancient lithospheric mantle and hot melt derived from recycling lower crust in Early Cretaceous. After that a fertile mantle was accreted from upwelling asthenosphere, which accomplished the replacement of the NCC lithsospheric mantle. Reference: Liang et al., 2013, A REE-in-two-pyroxene thermometer for mafic and ultramafic rocks. Geochimica et Cosmochimia Acta 102, 246-260.

  20. 3D representation of geochemical data, the corresponding alteration and associated REE mobility at the Ranger uranium deposit, Northern Territory, Australia

    NASA Astrophysics Data System (ADS)

    Fisher, Louise A.; Cleverley, James S.; Pownceby, Mark; MacRae, Colin

    2013-12-01

    Interrogation and 3D visualisation of multiple multi-element data sets collected at the Ranger 1 No. 3 uranium mine, in the Northern Territory of Australia, show a distinct and large-scale chemical zonation around the ore body. A central zone of Mg alteration, dominated by extensive clinochlore alteration, overprints a biotite-muscovite-K-feldspar assemblage which shows increasing loss of Na, Ba and Ca moving towards the ore body. Manipulation of pre-existing geochemical data and integration of new data collected from targeted `niche' samples make it possible to recognise chemical architecture within the system and identify potential fluid conduits. New trace element and rare earth element (REE) data show strong fractionation associated with the zoned alteration around the deposit and with fault planes that intersect and bound the deposit. Within the most altered portion of the system, isocon analysis indicates addition of elements including Mg, S, Cu, Au and Ni and removal of elements including Ca, K, Ba and Na within a zone of damage associated with ore precipitation. In the more distal parts of the system, processes of alteration and replacement associated with the mineralising system can be recognised. REE element data show enrichment in HREE centred about a characteristic peak in Dy in the high-grade ore zone while LREEs are enriched in the outermost portions of the system. The patterns recognised in 3D in zoning of geochemical groups and contoured S, K and Mg abundance and the observed REE patterns suggest a fluid flow regime in which fluids were predominately migrating upwards during ore deposition within the core of the ore system.

  1. 2nd International Symposium on Fundamental Aspects of Rare-earth Elements Mining and Separation and Modern Materials Engineering (REES-2015)

    NASA Astrophysics Data System (ADS)

    Tavadyan, Levon, Prof; Sachkov, Viktor, Prof; Godymchuk, Anna, Dr.; Bogdan, Anna

    2016-01-01

    The 2nd International Symposium «Fundamental Aspects of Rare-earth Elements Mining and Separation and Modern Materials Engineering» (REES2015) was jointly organized by Tomsk State University (Russia), National Academy of Science (Armenia), Shenyang Polytechnic University (China), Moscow Institute of Physics and Engineering (Russia), Siberian Physical-technical Institute (Russia), and Tomsk Polytechnic University (Russia) in September, 7-15, 2015, Belokuriha, Russia. The Symposium provided a high quality of presentations and gathered engineers, scientists, academicians, and young researchers working in the field of rare and rare earth elements mining, modification, separation, elaboration and application, in order to facilitate aggregation and sharing interests and results for a better collaboration and activity visibility. The goal of the REES2015 was to bring researchers and practitioners together to share the latest knowledge on rare and rare earth elements technologies. The Symposium was aimed at presenting new trends in rare and rare earth elements mining, research and separation and recent achievements in advanced materials elaboration and developments for different purposes, as well as strengthening the already existing contacts between manufactures, highly-qualified specialists and young scientists. The topics of the REES2015 were: (1) Problems of extraction and separation of rare and rare earth elements; (2) Methods and approaches to the separation and isolation of rare and rare earth elements with ultra-high purity; (3) Industrial technologies of production and separation of rare and rare earth elements; (4) Economic aspects in technology of rare and rare earth elements; and (5) Rare and rare earth based materials (application in metallurgy, catalysis, medicine, optoelectronics, etc.). We want to thank the Organizing Committee, the Universities and Sponsors supporting the Symposium, and everyone who contributed to the organization of the event and to

  2. Tracing the composition and origin of fluids at an ancient hydrocarbon seep (Hollard Mound, Middle Devonian, Morocco): A Nd, REE and stable isotope study

    NASA Astrophysics Data System (ADS)

    Jakubowicz, M.; Dopieralska, J.; Belka, Z.

    2015-05-01

    For the first time, Nd isotope signatures combined with rare earth element (REE) concentrations were used in investigations of ancient seep carbonates. The study was performed on the fossil hydrocarbon seep deposit of the Middle Devonian Hollard Mound (eastern Anti-Atlas, Morocco), where Nd isotopes, REE concentrations, and carbon and oxygen isotope ratios were measured to investigate the origin, former migration pathways and composition of fluids. Relatively high εNd values compared to local Eifelian seawater, as well as consistently appearing positive Eu anomalies in MREE-enriched shale-normalized REE patterns of the seep carbonates provided evidence for interaction between the seeping fluids and the Lower Devonian basaltic volcaniclastics underlying the studied seep deposit. Strongly reducing conditions and increased temperature of methane formation could have constituted an additional factor in the Eu-enrichment of the investigated carbonate phases. The presence of exclusively negative Ce anomalies in these carbonates is in line with observations of other workers that seep limestones may not necessarily display positive Ce anomalies indicative of precipitation under anoxic conditions. The negative Ce anomalies are attributed here to mixing between anoxic pore waters and oxic, Ce-depleted seawater, necessary to enable carbonate precipitation at seeps. The methane-rich fluids ascended most likely from below the volcaniclastic unit and inherited the enriched εNd signatures and positive Eu anomalies due to fluid-rock interactions during their seepage to the seafloor. The carbon isotope data are most consistent with thermogenic origin of methane, although contribution of abiotic and biogenic methane sources cannot be excluded. Our results indicate that neodymium isotope and rare earth element analyses constitute one of the most valuable tools for reconstructing former fluid migration patterns. The study shows also that Nd isotopes and Eu anomalies can serve as

  3. Water mass provenance and mixing in the Fram Strait, Arctic Ocean - Multi-proxy evidence from dissolved Nd isotopes, REEs, Ba, nutrients, and δ18O

    NASA Astrophysics Data System (ADS)

    Laukert, G.; Frank, M.; Hathorne, E. C.; Bauch, D.; Wegner, C.; Cao, Z.; Zieringer, M.; Andersen, N.; Kassens, H.

    2014-12-01

    Dissolved radiogenic Nd isotopes (ɛNd), rare earth element (REE), Ba, and nutrient concentrations combined with oxygen isotopes retrieved along a section between Spitsbergen and Greenland at approximately 79°N during the ARK XXVII/1 cruise in 2012 were measured to characterize the origin and mixing of the water masses in the Fram Strait. Deep waters below 500 m are nearly constant in Nd concentration (CNd) around 16 pmol/kg and ɛNd signatures range from -9.5±0.2 to -10.9±0.2. The heavy REE to light REE ratio (HREE/LREE) ranges from 4 to 5. Ba concentrations range from 47 to 58 nmol/kg, increasing slightly with depth. These homogeneous signatures do not allow identification of distinct deep water masses. The upper 500 m of the water column close to the Western Svalbard margin including the shelf is relatively warm and saline (T ≤ 5.5°C, S ≤ 35.1) and shares characteristics of Atlantic Water (AW) including low CNd (~15 pmol/kg) and relatively unradiogenic ɛNd signatures (-12.2±0.2). This water is also characterized by HREE/LREE around 4 and CBa around 50 nmol/kg. Low salinity surface waters on the East Greenland shelf have unradiogenic ɛNd signatures similar to AW (-12.4±0.3) but in contrast to AW high CNd of up to 37 pmol/kg. At the same time the HREE/LREE ratio is relatively low (~3.5) and CBa reaches 73 nmol/kg. This suggests a significant freshwater contribution either from the McKenzie or the Lena rivers. Eastwards of these freshwater-influenced waters (at ~5°W), admixture of a Pacific component characterized by a more radiogenic ɛNd (-8.8±0.2) and high nutrient concentrations outcropping at surface was detected. Waters of the same origin are present on the East Greenland shelf at about 150 m depth. Based on these data we use mass balance calculations to determine the fractions of sea ice meltwater, Eurasian run-off, North American run-off, and Arctic seawater and compare these results with our ɛNd and REE data.

  4. REE Sorption Study on sieved -50 +100 mesh fraction of Media #1 in Brine #1 with Different Starting pH's at 70C

    SciTech Connect

    Gary Garland

    2015-09-29

    This is a continuation of the REE sorption study for shaker bath tests on 2g media #1 in 150mL brine #1 with different starting pH's at 70C. In a previous submission we reported data for shaker bath tests for brine #1 with starting pH's of 3.5, 4.5 and 5.5. In this submission we these pH's compared to starting brine #1 pH's of 6, and 7.

  5. Observations and analysis with the spline-based Rydberg-Klein-Rees approach for the 3(1)Σg(+) state of Rb2.

    PubMed

    Yang, Jinxin; Guan, Yafei; Zhao, Wei; Zhou, Zhaoyu; Han, Xiaomin; Ma, Jie; Sovkov, Vladimir B; Ivanov, Valery S; Ahmed, Ergin H; Lyyra, A Marjatta; Dai, Xingcan

    2016-01-14

    Ro-vibrational term values of the 3(1)Σg (+) state of (85,85)Rb2 and (85,87)Rb2 and resolved fluorescence spectra to the A(1)Σu (+) state are recorded following optical-optical double resonance excitation. The experimental data are heavily perturbed, and as a result, the standard analysis based on Dunham series representation of the energy levels fails. The analysis is done via modeling the adiabatic potential function with the Rydberg-Klein-Rees potential constructed from the generalized smoothing spline interpolation of the vibrational energies Gv and rotational constants Bv. PMID:26772572

  6. Distribution of trace elements including tellurium, gallium, indium, and select REE in sulfide chimneys from Brothers submarine volcano, Kermadec arc

    NASA Astrophysics Data System (ADS)

    Berkenbosch, H. A.; de Ronde, C. E.; McNeill, A.; Goemann, K.; Gemmell, J. B.

    2011-12-01

    -rich chimney also contained native Te in a similar distribution as the tellurides. Whole rock geochemical analysis has determined the maximum concentration of trace elements and REE such as In (53.1 ppm), Ga (1870), Y (26), La (21.2), Ce (21), Sm (2.8), Gd (4), and Yb (3) in Brothers chimneys. To better understand the mineral associations and zonation of these and other trace elements within the chimney walls, we have undertaken element mapping on the four different chimneys types with both X-Ray fluorescence microscopy using synchrotron radiation and with Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICPMS). For example, in a chalcopyrite-rich chimney visibly laminated chalcopyrite in the interior contains bands of Co, Mo, Ag, Te, Au, and Bi, whereas In, La, Ce, Ga, and Y are concentrated in other mineral phases towards the exterior. Element mapping allows us to better understand the physico-chemical gradients within chimney walls, as well as metal sources and transportation, and depositional processes.

  7. U, Th, Pb and REE abundances and Pb 207/Pb 206 ages of individual minerals in returned lunar material by ion microprobe mass analysis.

    NASA Technical Reports Server (NTRS)

    Andersen, C. A.; Hinthorne, J. R.

    1972-01-01

    Results of ion microprobe analyses of Apollo 11, 12 and 14 material, showing that U, Th, Pb and REE are concentrated in accessory minerals such as apatite, whitlockite, zircon, baddeleyite, zirkelite, and tranquillityite. Th/U ratios are found to vary by over a factor of 40 in these minerals. K, Ba, Rb and Sr have been localized in a K rich, U and Th poor glass phase that is commonly associated with the U and Th bearing accessory minerals. Li is observed to be fairly evenly distributed between the various accessory phases. The phosphates have been found to have REE abundance patterns (normalized to the chondrite abundances) that are fairly flat, while the Zr bearing minerals have patterns that rise steeply, by factors of ten or more, from La to Gd. All the accessory minerals have large negative Eu anomalies. Radiometric age dates (Pb 207/Pb 206) of the individual U and Th bearing minerals compare favorably with the Pb 207/Pb 206 age of the bulk rocks.

  8. Petrography and the REE-composition of apatite in the Paleoproterozoic Pilgujärvi Sedimentary Formation, Pechenga Greenstone Belt, Russia

    NASA Astrophysics Data System (ADS)

    Joosu, Lauri; Lepland, Aivo; Kreitsmann, Timmu; Üpraus, Kärt; Roberts, Nick M. W.; Paiste, Päärn; Martin, Adam P.; Kirsimäe, Kalle

    2016-08-01

    The first globally significant phosphorous-rich deposits appear in the Paleoproterozoic at around 2 Ga, however, the specific triggers leading to apatite precipitation are debated. We examine phosphorous-rich rocks (up to 8 wt% P2O5) in 1.98-1.92 Ga old Pilgujärvi Sedimentary Formation, Pechenga Greenstone Belt, Russia. Phosphates in these rocks occur as locally derived and resedimented sand-to-gravel/pebble sized grains consisting of apatite-cemented muddy sediments. Phosphatic grains can be subdivided into four petrographic types (A-D), each has a distinct REE signature reflecting different early-to-late diagenetic conditions and/or metamorphic overprint. Pyrite containing petrographic type D, which typically has a flat REE pattern, negative Ce anomaly and positive Eu anomaly, is the best preserved of the four types and best records conditions present during apatite precipitation. Type D phosphatic grains precipitated under (sub)oxic basinal conditions with a significant hydrothermal influence. These characteristics are similar to Zaonega Formation phosphates of NW Russia's Onega Basin, and consistent with phosphogenesis triggered by the development of anoxic(sulfidic)-(sub)oxic redoxclines at shallow sediment depth during the Paleoproterozoic.

  9. Efremovka 101.1: a CAI with ultrarefractory REE patterns and enormous enrichments of Sc, Zr, and Y in Fassaite and Perovskite

    NASA Astrophysics Data System (ADS)

    El Goresy, A.; Zinner, E.; Matsunami, S.; Palme, H.; Spettel, B.; Lin, Y.; Nazarov, M.

    2002-04-01

    Inclusion 101.1 from the CV3 carbonaceous chondrite Efremovka is a compact Type A Ca-Al-rich inclusion (CAI) highly enriched in ultrarefractory (UR) oxides. It is the first complete CAI with a UR rare earth element (REE) pattern found in a CV3 chondrite. The inclusion is petrographically complex and was formed in a multistage process. It consists of several lithologically unrelated units. The core contains abundant Y- and Zr-perovskite, Sc- and Zr-rich fassaite, and metallic FeNi enclosed in melilite. All mineral species (except spinel) in all lithological units exhibit the same basic UR REE pattern. Four different populations of perovskites are distinguished by different Y/Zr ratios. A few of the perovskites have Y/Zr ratios similar to those obtained from crystal/liquid fractionation experiments. Perovskites from the other three populations have either chondritic, lower than chondritic Y/Zr ratios or extremely low Zr contents. Ca isotopic ratios differ among three perovskites from different populations, demonstrating a variety of sources and formational processes. Most fassaites crystallized in situ through reaction between the CAI liquid and preexisting perovskites. This process induced redistribution of Zr, Y, Sc, and V between perovskite and fassaite, thus overprinting the original abundances in perovskite. Fassaite reaction rims around FeNi metals are also encountered. They are enriched in V, which was gained from the metal through oxidation of V in metal during fassaite crystallization. The relative abundances of Zr, Y, and Sc in perovskites are complementary to the abundances of these elements in Sc- and Zr-fassaite, indicating subsolidus partitioning of these elements between the two phases. Perovskites are enriched in Y and depleted in Sc and Zr in comparison to fassaites. The core contains two complete captured CAIs, several sinuous fragments, and fine-grained polygonal refractory fragments. An assemblage of andradite-wollastonite-hedenbergite and pure

  10. Percolation of enriched melts during incremental open-system melting in the spinel field: A REE approach to abyssal peridotites from the Southwest Indian Ridge

    NASA Astrophysics Data System (ADS)

    Brunelli, Daniele; Paganelli, Emanuele; Seyler, Monique

    2014-02-01

    The effects of melting in an open-system scenario are here explored looking to the rare earth element (REE) distribution in mantle residues. We consider a peridotite matrix equilibrated in the spinel field accounting for melt inflow during partial melting. The fertility of the source, inflowing melt composition and melt addition rate as well as the effects of varying the critical mass porosity in an incremental scenario are tested. When a relatively enriched melt enters the system, residual clinopyroxene REE normalized patterns apparently rotate around a light to intermediate REE due to concomitant increase of the light REEs and decrease of the heavy REEs. This effect is enhanced when the critical mass porosity is large with respect to the degree of melting. In these cases the system approaches batch more than fractional melting behaviour because the liquid is preferentially retained in the matrix. This geometry is suggestive of melt accumulation at depth. Four sample suites from the Southwest Indian Ridge are considered. Spinel field equilibrated clinopyroxenes in lherzolites and harzburgites show dredge-scale REE compositional trends that crosscut model fractional melting trajectories. Observed local trends correspond to rotations of the REE patterns attesting for near-batch episodes in the subridge melting history and infiltration of enriched liquids whose composition resemble that of garnet field-generated melts. C0: starting source composition. D0: starting bulk partition coefficient. P: bulk partition coefficient weighted for the mineral melting mode (modal melting for P = D). Ca: is the tracer concentration in the inflowing melt. The composition of the liquid produced during non-modal melting is estimated by using equation (30) of Shaw (2000): {C}/{C}={C}/{0lC}-{β}/{(1+β)(1-P)}{C}/{C}1+{β}/{(1+β)(1-P)}{Ca}/{C0} The composition of the solid in equilibrium with the liquid is Cs = DCL, where D is the bulk partition coefficient for a given element

  11. Stages of weathering mantle formation from carbonate rocks in the light of rare earth elements (REE) and Sr-Nd-Pb isotopes

    NASA Astrophysics Data System (ADS)

    Hissler, Christophe; Stille, Peter

    2015-04-01

    Weathering mantles are widespread and include lateritic, sandy and kaolinite-rich saprolites and residuals of partially dissolved rocks. These old regolith systems have a complex history of formation and may present a polycyclic evolution due to successive geological and pedogenetic processes that affected the profile. Until now, only few studies highlighted the unusual high content of associated trace elements in weathering mantles originating from carbonate rocks, which have been poorly studied, compared to those developing on magmatic bedrocks. For instance, these enrichments can be up to five times the content of the underlying carbonate rocks. However, these studies also showed that the carbonate bedrock content only partially explains the soil enrichment for all the considered major and trace elements. Up to now, neither soil, nor saprolite formation has to our knowledge been geochemically elucidated. Therefore, the aim of this study was to examine more closely the soil forming dynamics and the relationship of the chemical soil composition to potential sources. REE distribution patterns and Sr-Nd-Pb isotope ratios have been used because they are particularly well suited to identify trace element migration, to recognize origin and mixing processes and, in addition, to decipher possible anthropogenic and/or "natural" atmosphere-derived contributions to the soil. Moreover, leaching experiments have been applied to identify mobile phases in the soil system and to yield information on the stability of trace elements and especially on their behaviour in these Fe-enriched carbonate systems. All these geochemical informations indicate that the cambisol developing on such a typical weathering mantle ("terra fusca") has been formed through weathering of a condensed Bajocian limestone-marl facies. This facies shows compared to average world carbonates important trace element enrichments. Their trace element distribution patterns are similar to those of the soil

  12. Structural controls and evolution of gold-, silver-, and REE-bearing copper-cobalt ore deposits, Blackbird district, east-central Idaho: Epigenetic origins

    USGS Publications Warehouse

    Lund, K.; Tysdal, R.G.; Evans, K.V.; Kunk, M.J.; Pillers, R.M.

    2011-01-01

    Textural data at all scales indicate that the host sites for veins and the tectonic evolution of both host rocks and mineral deposits were kinematically linked to Late Cretaceous regional thrust faulting. Heat, fluids, and conduits for generation and circulation of fluids were part of the regional crustal thickening. The faulting also juxtaposed metaevaporite layers in the Mesoproterozoic Yellowjacket Formation over Blackbird district host rocks. We conclude that this facilitated chemical exchange between juxtaposed units resulting in leaching of critical elements (Cl, K, B, Na) from metaevaporites to produce brines, scavenging of metals (Co, Cu, etc) from rocks in the region, and, finally, concentrating metals in the lower-plate ramp structures. Although the ultimate source of the metals remains undetermined, the present Cu-Co ± Au (± Ag ± Ni ± REE) Blackbird ore deposits formed during Late Cretaceous compressional deformation.

  13. An ion microprobe study of the intra-crystalline behavior of REE and selected trace elements in pyroxene from mare basalts with different cooling and crystallization histories

    NASA Technical Reports Server (NTRS)

    Shearer, C. K.; Papike, J. J.; Simon, S. B.; Shimizu, N.

    1989-01-01

    The effects of crystallization interaction on the trace element zoning characteristics of pyroxenes are analyzed using electron and ion microprobe techniques. Four pigeonite basalts with similar isochemical composition, but different cooling rates and crystallization histories are studied. Pyroxene quadrilaterals displaying crystallization trends are presented. The crystal chemical rationalization of REE zoning, pattern shapes, and abundances are examined. The data reveal that the trace element zoning characteristics in pyroxene and the partitioning of trace elements between pyroxene and the melt are related to the interaction between the efficiency of the crystallization process, the kinetics at the crystal-melt interface, the kinetics of plagioclase nucleation and the characteristics of the crystal chemical substitutions in the pyroxene and the associated crystallizing phase.

  14. A late Triassic 40Ar/39Ar age for the El Hammam high-REE fluorite deposit (Morocco): mineralization related to the Central Atlantic Magmatic Province?

    NASA Astrophysics Data System (ADS)

    Cheilletz, Alain; Gasquet, Dominique; Filali, Fouad; Archibald, Douglas A.; Nespolo, Massimo

    2010-04-01

    El Hammam is the only fluorite mine in Morocco (production 100,000 t/year). The fluorite mineralization is in an array of fluorite-calcite veins and is characterized by unusually high REE content in carbonate minerals (1,400 ppm in calcite; up to 2,000 ppm in siderite) and in fluorite (about 600 ppm). Since the 1960s, the genesis of the deposit has been attributed to a mesothermal hydrothermal event connected with late-Variscan granitic intrusions. Precise 40Ar/39Ar dating of hydrothermal K-feldspar yields an age of formation of the El Hammam deposit at 205 ± 1 Ma. Its genesis is therefore associated in time and space with the development of the Triassic-Jurassic basins and the associated anorogenic continental flood basalts of the Moroccan Mesetian Middle Atlas. The source of the hydrothermal mineralization (magmatic and/or metamorphic) is discussed.

  15. An assessment of a handheld X-ray fluorescence instrument for use in exploration and development with an emphasis on REEs and related specialty metals

    NASA Astrophysics Data System (ADS)

    Simandl, G. J.; Stone, R. S.; Paradis, S.; Fajber, R.; Reid, H. M.; Grattan, K.

    2014-12-01

    Handheld (portable) X-ray fluorescence (pXRF) instruments are designed for use in the exploration for base metals, precious metals, and specialty metals (e.g. rare earth elements (REE), Ta, and Nb) and allow rapid decision-making directly in the field. This paper evaluates the technical merits and limitations of pXRF technology in the exploration for specialty metals using data generated from the analysis of three geochemical standards and a silica blank: Standard Reference Material NIST 2780 from the National Institute of Standards and Technology, Gaithersburg; the Certified Reference Material "TRLK" Rare Earth Ore "CGL 124" from the Mongolia Central Geological Laboratory; the Reference Niobium Ore OKA-1 (CANMET); and a silica blank described as Si (IV) oxide (99.8 % on metal basis) from Alpha Aesar (Ward Hill, MA, USA). The data was acquired over a period of nearly 2 years as a by-product of several distinct specialty metal-related projects using the same pXRF instrument and the same settings. Instrumental analytical accuracy was determined using the percent difference (%diff) between the average concentrations of the pXRF instrument readings and the reported certified values of the standard. Percent relative standard deviation (%RSD) was used as a measure of precision. Smaller %diff and %RSD indicate more accurate and precise data, and the accuracy and precision of the pXRF depended strongly on the elemental concentrations in the standards used. Box and whisker diagrams were used to illustrate characteristics of pXRF data sets (mean, lower and upper quartiles, and range) corresponding to individual standards. The bias of the pXRF determinations (under/overestimation) relative to certified values of individual standards are also depicted on these diagrams. This study indicates that the pXRF was capable of producing readings for Si, K, Al, Fe, Ca, Ti, Pb, Zn, Sr, Ag, Cd, Th, Sb, P, S, Mo, Mn, Mg, As, Nb, Rb, La, Ce, Pr, Nd, and Y within 10 %RSD of the reported

  16. Major element, REE, and Pb, Nd and Sr isotopic geochemistry of Cenozoic volcanic rocks of eastern China: implications for their origin from suboceanic-type mantle reservoirs

    USGS Publications Warehouse

    Basu, A.R.; Wang, Junwen; Huang, Wankang; Xie, Guanghong; Tatsumoto, M.

    1991-01-01

    Major- and rare-earth-element (REE) concentrations and UThPb, SmNd, and RbSr isotope systematics are reported for Cenozoic volcanic rocks from northeastern and eastern China. These volcanic rocks, characteristically lacking the calc-alkaline suite of orogenic belts, were emplaced in a rift system which formed in response to the subduction of the western Pacific plate beneath the eastern Asiatic continental margin. The rocks sampled range from basanite and alkali olivine basalt, through olivine tholeiite and quartz tholeiite, to potassic basalts, alkali trachytes, pantellerite, and limburgite. These rock suites represent the volcanic centers of Datong, Hanobar, Kuandian, Changbaishan and Wudalianchi in northeastern China, and Mingxi in the Fujian Province of eastern China. The major-element and REE geochemistry is characteristic of each volcanic suite broadly evolving through cogenetic magmatic processes. Some of the outstanding features of the isotopic correlation arrays are as follows: (1) NdSr shows an anticorrelation within the field of ocean island basalts, extending from the MORB end-member to an enriched, time-averaged high Rb Sr and Nd Sr end-member (EM1), (2) SrPb also shows an anticorrelation, similar to that of Hawaiian and walvis Ridge basalts, (3) NdPb shows a positive correlation, and (4) the 207Pb 204Pb vs 206Pb 204Pb plot shows linear arrays parallel to the general trend (NHRL) for MORB on both sides of the geochron, although in the 208Pb 204Pb vs 206Pb 204Pb plot the linear array is significantly displaced above the NHRL in a pattern similar to that of the oceanic island basalts that show the Dupal signatures. In all isotope correlation patterns, the data arrays define two different mantle components-a MORB-like component and an enriched mantle component. The isotopic data presented here clearly demonstrate the existence of Dupal compositions in the sources of the continental volcanic rocks of eastern China. We suggest that the subcontinental mantle

  17. Experimental study of polybaric REE partitioning between olivine, pyroxene and melt of the Yamato 980459 composition: Insights into the petrogenesis of depleted shergottites

    NASA Astrophysics Data System (ADS)

    Blinova, Alexandra; Herd, Christopher D. K.

    2009-06-01

    A synthetic composition representing the Yamato 980459 martian basalt (shergottite) has been used to carry out phase relation, and rare earth element (REE) olivine and pyroxene partitioning experiments. Yamato 980459 is a sample of primitive basalt derived from a reduced end-member among martian mantle sources. Experiments carried out between 1-2 GPa and 1350-1650 °C simulate the estimated pressure-temperature conditions of basaltic melt generation in the martian mantle. Olivine-melt and orthopyroxene-melt partition coefficients for La, Nd, Sm, Eu, Gd and Yb ( DREE values) were determined by LA-ICPMS, and are similar to the published values for terrestrial basaltic systems. We have not detected significant variation in D-values with pressure over the range investigated, and by comparison with previous studies carried out at lower pressure. We apply the experimentally obtained olivine-melt and orthopyroxene-melt DREE values to fractional crystallization and partial melting models to develop a three-stage geochemical model for the evolution of martian meteorites. In our model we propose two ancient (˜4.535 Ga) sources: the Nakhlite Source, located in the shallow mantle, and the Deep Mantle Source, located close to the martian core-mantle boundary. These two sources evolved distinctly on the ɛ 143Nd evolution curve due to their different Sm/Nd ratios. By partially melting the Nakhlite Source at ˜1.3 Ga, we are able to produce a slightly depleted residue (Nakhlite Residue). The Nakhlite Residue is left undisturbed until ˜500 Ma, at which point the depleted Deep Mantle Source is brought up by a plume mechanism carrying with it high heat flow, melts and isotopic signatures of the deep mantle (e.g., ɛ 182W, ɛ 142Nd, etc.). The plume-derived Deep Mantle Source combines with the Nakhlite Residue producing a mixture that becomes a mantle source (herein referred to as "the Y98 source") for Yamato 980459 and the other depleted shergottites with the characteristic range

  18. Ion Microprobe U-Pb Dating and REE Analysis of Apatite from Kerogen-rich Silica Dike from North Pole Area, Pilbara Craton, Western Australia

    NASA Astrophysics Data System (ADS)

    Nishizawa, M.

    2003-12-01

    In order to provide a time constraint on the 13C-depleted kerogen in silica dikes that intruded 3.5 Ga greenstone from Pilbara Craton in Western Australia, we have carried out an ion microprobe U-Pb dating and rare earth element (REE) analysis of apatite from the dike. Two types of apatite were identified in the dikes based on their occurrences. One is stick-shape apatites (Type 1) in secondary silica micro-veins that cut the silica dike. The other is granular apatites (Type 2) that occurs in matrix of the dike. Occurrence in the secondary micro-veins (Type 1), non-igenous chondrite normalized REE patterns (Type 1 and 2), chemical zoning (some of Type 1 and 2), and presence of mineral inclusion that is composed of Fe and S (some of Type 2) suggest that both Type 1 and 2 apatites were crystallized in the silica dike. Ion microprobe U-Pb dating of Type 1 apatite did not give a meaningful age, while Type 2 apatite yields a Tera-Wasserburg concordia intercept age of 3214 +/- 140 Ma (95 per cent confidence level, MSWD = 0.6) in a three-dimensional 238U/206Pb-207Pb/206Pb-204Pb/206Pb diagram, and a 204Pb/206Pb-207Pb/206Pb isochron age of 3191 +/- 150 Ma (95 per cent confidence level, MSWD = 0.5). It is difficult to judge whether the U-Pb and Pb-Pb age of Type 2 apatite is crystallization age or metamorphic age, since the estimated range of closure temperature of U-Pb system in the apatite and that of metamorphic temperature is partly overlapped. In either case, it can be safely concluded that the minimum age of the dike and kerogen is 3.0 Ga. These ages might allow the interpretation that the kerogen was produced by biological carbon fixation and/or abiological reaction (such as Fischer-Tropsch Type reaction) at least before 3.0 Ga.

  19. Distributions of REE, Nd, Hf and Pb isotopes in the surfaces of Fe-Mn crusts from across the Pacific Ocean

    NASA Astrophysics Data System (ADS)

    Chu, N.; Nesbitt, R. W.; German, C. R.; Halbach, P.

    2001-12-01

    Over the past decade, numerous studies have investigated radiogenic isotopes (i.e. Nd, Pb, Hf, Os) in marine Fe-Mn deposits in an attempt to infer changes in ocean circulation throughout the Cenozoic. The use of radiogenic isotopes as paleoceanographic proxies has been challenged recently by evidence that the isotopic composition of crusts from oceanic domains near major river systems (e.g. Amazon, Congo) or old cratonic areas (i.e. the North Atlantic area) could be influenced significantly by continental inputs. Therefore, for any given crust, it is difficult to deduce the extent to which changes in weathering processes rather than ocean circulation may be responsible for observed isotopic variations. This is partly due to the fact that the oceanic budgets for some of these elements remain poorly constrained. In particular, the influence of both the eastward aeolian transport of Chinese loess and the erosion of the young West-Pacific volcanic belt on the isotopic composition of Pacific water masses has been poorly documented. The deep Pacific Ocean is composed of 4 principal water masses: North Pacific Intermediate Water (NPIW), Antarctic Intermediate Water (AAIW), Pacific Deep Water (PDW) and Antarctic Bottom Water (AABW). AABW, the main source of PDW, flows northward and enters the Central Basin through the Samoan Passage, where it is diverted into two branches: eastward to Line Island Passage and westward through Wake Passage. We will present Nd, Hf and Pb isotopic ratios combined with REE data from the surfaces of 16 Fe-Mn crusts taken at different depths from key areas of the Pacific Ocean. Two crusts were collected from the Izu-Bonin back-arc basin in the western Pacific and, hence, are particularly suitable for monitoring the influence of both continental aeolian and weathering inputs. Two other groups of crusts are from north and south of the equatorial Pacific region. The southern group is situated at the exit of the Samoan Passage, whereas the northern

  20. Detrital zircon U-Pb geochronology, Lu-Hf isotopes and REE geochemistry constrains on the provenance and tectonic setting of Indochina Block in the Paleozoic

    NASA Astrophysics Data System (ADS)

    Wang, Ce; Liang, Xinquan; Foster, David A.; Fu, Jiangang; Jiang, Ying; Dong, Chaoge; Zhou, Yun; Wen, Shunv; Van Quynh, Phan

    2016-05-01

    In situ U-Pb geochronology, Lu-Hf isotopes and REE geochemical analyses of detrital zircons from Cambrian-Devonian sandstones in the Truong Son Belt, central Vietnam, are used to provide the information of provenance and tectonic evolution of the Indochina Block. The combined detrital zircon age spectra of all of the samples ranges from 3699 Ma to 443 Ma and shows with dominant age peaks at ca. 445 Ma and 964 Ma, along with a number of age populations at 618-532 Ma, 1160-1076 Ma, 1454 Ma, 1728 Ma and 2516 Ma. The zircon age populations are similar to those from time equivalent sedimentary sequences in continental blocks disintegrated from the East Gondwana during the Phanerozoic. The younger zircon grains with age peaks at ca. 445 Ma were apparently derived from middle Ordovician-Silurian igneous and metamorphic rocks in Indochina. Zircons with ages older than about 600 Ma were derived from other Gondwana terrains or recycled from the Precambrian basement of the Indochina Block. Similarities in the detrital zircon U-Pb ages suggest that Paleozoic strata in the Indochina, Yangtze, Cathaysia and Tethyan Himalayas has similar provenance. This is consistent with other geological constrains indicating that the Indochina Block was located close to Tethyan Himalaya, northern margin of the India, and northwestern Australia in Gondwana.

  1. Proterozoic seawater — felsic volcanics interaction W. Bergslagen, Sweden. Evidence for high REE mobility and implications for 1.8 Ga seawater compositions

    NASA Astrophysics Data System (ADS)

    Baker, James H.; de Groot, Pier A.

    1983-06-01

    Mg enrichment in diffusely bounded, schistose alteration zones occurring in Proterozoic submarine felsic volcanics NE of Hjulsjö, W. Bergslagen is shown to result from felsic rock-seawater interaction in a sub-seafloor hydrothermal system. The alteration is apparently in two stages, feldspar being altered first to a kaolinite-type clay which is then replaced by Mg-chlorite. Major and trace element data are presented for the schist and sheridanite (chlorite). Relative to the least altered felsic volcanics, and for negligible volume change, the schist shows strong addition of Mg and to a lesser extent Si; K, Al and Rb are apparently conserved, while most other elements are strongly depleted, including the REEs which are removed for ˜75%, indicating a high degree of mobility. The chlorite, with its HREE enriched pattern, is considered to have equilibrated with the hydrothermal fluid, which consisted predominantly of seawater. Comparison with modern seawater leads to the tentative conclusion that the Proterozoic seawater HREE composition was not drastically different from that of modern seawater.

  2. Iron isotope and REE+Y composition of the Cauê banded iron formation and related iron ores of the Quadrilátero Ferrífero, Brazil

    NASA Astrophysics Data System (ADS)

    Mendes, Mônica; Lobato, Lydia M.; Kunzmann, Marcus; Halverson, Galen P.; Rosière, Carlos A.

    2016-04-01

    The Minas Supergroup banded iron formations (BIFs) of the Brazilian Quadrilátero Ferrífero (QF) mineral province experienced multiple deformational events synchronous with hypogene mineralization, which resulted in the metamorphism of BIFs to itabirites and their upgrade to high-grade iron ore. Here, we present rare earth element and yttrium (REE+Y) compositions together with iron isotope ratios of itabirites and their host iron orebodies from 10 iron deposits to constrain environmental conditions during BIF deposition and the effects of hypogene iron enrichment. The REE+Y characteristics of itabirites (positive Eu anomaly and LREE depletion) indicate hydrothermal iron contribution to the Minas basin. Iron isotope data and Ce anomalies suggest BIFs were precipitated by a combination of anoxic biological-mediated ferrous iron oxidation and abiotic oxidation in an environment with free oxygen (such as an oxygen oasis), perhaps related to increase in oxygen concentrations before the Great Oxidation Event (GOE). The similarity of the REE+Y composition of the itabirites from the different QF deformational domains, as well as to other Superior-type BIFs, indicates that the metamorphism and synchronous hydrothermal mineralization did not significantly affect the geochemical signature of the original BIFs. However, iron isotope compositions of iron ore vary systematically between deformational domains of the QF, likely reflecting the specific mineralization features in each domain.

  3. Multistage hydrothermal silicification and Fe-Tl-As-Sb-Ge-REE enrichment in the Red Dog Zn-Pb-Ag district, northern Alaska: Geochemistry, origin, and exploration applications

    USGS Publications Warehouse

    Slack, J.F.; Kelley, K.D.; Anderson, V.M.; Clark, J.L.; Ayuso, R.A.

    2004-01-01

    Geochemical analyses of major, trace, and rare earth elements (REE) in more than 200 samples of variably silicified and altered wall rocks, massive and banded sulfide, silica rock, and sulfide-rich and unmineralized barite were obtained from the Main, Aqqaluk, and Anarraaq deposits in the Red Dog Zn-Pb-Ag district of northern Alaska. Detailed lithogeochemical profiles for two drill cores at Aqqaluk display an antithetic relationship between SiO2/Al2O3 and TiO2/Zr which, together with textural information, suggest preferential silicification of carbonate-bearing sediments. Data for both drill cores also show generally high Tl, Sb, As, and Ge and uniformly positive Eu anomalies (Eu/Eu* > 1.0). Similar high Tl, Sb, As, Ge, and Eu/Eu* values are present in the footwall and shallow hanging wall of Zn-Pb-Ag sulfide intervals at Anarraaq but are not as widely dispersed. Net chemical changes for altered wall rocks in the district, on the basis of average Al-normalized data relative to unaltered black shales of the host Kuna Formation, include large enrichments (>50%) of Fe, Ba, Eu, V, S, Co, Zn, Pb, Tl, As, Sb, and Ge at both Red Dog and Anarraaq, Si at Red Dog, and Sr, U, and Se at Anarraaq. Large depletions (>50%) are evident for Ca at both Red Dog and Anarraaq, for Mg, P, and Y at Red Dog, and for Na at Anarraaq. At both Red Dog and Anarraaq, wall-rock alteration removed calcite and minor dolomite during hydrothermal decarbonation reactions and introduced Si, Eu, and Ge during silicification. Sulfidation reactions deposited Fe, S, Co, Zn, Pb, Tl, As, and Sb; barite mineralization introduced Ba, S, and Sr. Light REE and U were mobilized locally. This alteration and mineralization occurred during Mississippi an hydrothermal events that predated the Middle Jurassic-Cretaceous Brookian orogeny. Early hydrothermal silicification at Red Dog took place prior to or during massive sulfide mineralization, on the basis of the dominantly planar nature of Zn-Pb veins, which suggests

  4. Fluorescein Dye Penetration in Round Top Rhyolite (Hudspeth County, Texas, USA) to Reveal Micro-permeability and Optimize Grain Size for Heavy REE Heap Leach

    NASA Astrophysics Data System (ADS)

    Negron, L. M.; Clague, J. W.; Gorski, D.; Amaya, M. A.; Pingitore, N. E.

    2013-12-01

    Millimeter- and micrometer-scale permeability of fine-grained igneous rocks has generated limited research interest. Nonetheless, the scale and distribution of such micro-permeability determines fluid penetration and pathways, parameters that define both the ability to heap leach a rock and the optimal grain size for such an operation. Texas Rare Earth Resources is evaluating the possibility of heap leaching of yttrium and heavy rare earth elements (YHREE) from the peraluminous rhyolite laccolith that forms one-mile-diameter Round Top Mountain. The YHREEs in this immense, surface-exposed deposit (minimum 1.6 billion tons, Texas Bureau Economic Geology) are dilute and diffuse, suggesting leaching as the best option for recovery. The REE grade is 0.05% and YHREEs comprise more than 70% of the total REE content. The YHREEs are hosted exclusively in micron-scale yttrofluorite grains, which proved soluble in dilute sulfuric acid. Laboratory experiments showed YHREE recoveries of up to 90%. Within limits, recoveries decrease with larger grain sizes, and increase with acid strength and exposure time. Our research question centers on dissolution effectiveness: Is YHREE recovery, relative to grain size, limited by (1) diffusion time of acid into, and dissolved solids, including YHREEs, out of the micro-permeability paths inherent in the rock particles; (2) the effective lengths of the natural micro-permeability paths in the rock; or (3) the putative role of the acid in dissolving new micro-paths into the grains? The maximum grain size should not exceed twice the typical path length (unless acid creates new paths), lest YHREEs in the core of a larger grain than that not be reached by acid. If instead diffusion time is limiting, longer leach time may prove effective. Rather than perform an extensive and expensive series of laboratory leaching experiments--some of which would be several months in duration--to determine optimal grain size, we developed a technique to

  5. Metasomatic silicate chemistry at the Bayan Obo Fe REE Nb deposit, Inner Mongolia, China: Contrasting chemistry and evolution of fenitising and mineralising fluids

    NASA Astrophysics Data System (ADS)

    Smith, M. P.

    2007-01-01

    Fenite aureoles around carbonatite dykes, and alteration associated with Fe-REE-Nb ore bodies at Bayan Obo, Inner Mongolia, China, show alkali silicate assemblages containing aegirine-augite, (magnesio-)riebeckite, (magnesio-)arfvedsonite, and phlogopite, accompanied by varying amounts of apatite, albite and quartz. In both fenites and orebodies simple thermodynamic constraints indicate mineral parageneses are consistent with rock buffered cooling accompanied by the infiltration of a range of externally buffered hydrothermal fluids. Statistical analysis of amphibole chemistry indicates that even in apparently texturally well constrained paragenetic stages wide variations in chemistry occur in both the ore bodies and fenites. Much of this variation is attributable to the Mg and F content of amphibole, and is therefore interpreted as a result of variation in externally controlled variables ( P, T, initial fluid composition) rather than internally controlled variables such as protolith composition. Similarities in chemistry exist between fenite and some ore body amphiboles. Thermodynamic analysis of the composition of biotite and apatite allows constraints to be placed on the F-content of hydrothermal fluids, and indicates relatively consistent compositions in fenites and orebodies (log aHF/ aH 2O = - 3.8 to - 3.6 at 300 °C and 1 kbar). Amphibole and biotite associated with niobate mineralization are both enriched in fluorine relative to the rest of the paragenesis, and biotite compositions indicate significantly higher HF activities in the hydrothermal fluid (log aHF/ aH 2O = - 2.6 at 300 °C and 1 kbar). The data presented here reinforce previous interpretations of the complex, multistage nature of mineralisation at Bayan Obo, but are still consistent with a direct involvement of carbonatite derived fluids during ore genesis.

  6. Efremovka 101.1: A Primitive CAI with Superrefractory REE Patterns and Enormous Enrichments of Sc, Zr, and Y in Fassaite and Perovskite

    NASA Astrophysics Data System (ADS)

    El Goresy, A.; Zinner, E. K.; Matsunami, S.; Palme, H.; Spettel, B.; Lin, Y.; Nazarov, M.

    1993-07-01

    encountered inside the sinuous fragments and in the diopside-anorthite rim sequence of one of the captured CAIs. The texture is strongly suggestive of the reduction of andradite to wollastonite+Fe^degree (via Fe3O4 and FeO). We consider this texture as evidence that andradite was formed in an oxidizing solar gas before capture of the sinuous inclusions by the host CAI and that andradite reduction took place after capture in the highly reduced host CAI refractory liquid. REE concentrations in various minerals reveal a distinct superrefractory pattern with depletions in Tm and Yb. Zr, Y, and Sc abundances of individual phases in the CAI core are indicative of crystal-liquid fractionation during crystallization: fassaite is relatively depleted in Y and enriched in Sc and Zr. In contrast, perovskite displays a complimentary abundance pattern for these elements. The individual mineral layers of the captured CAIs, sinuous fragments, and the rim sequence of the host CAI have similar superrefractory REE patterns but do not show fractionation between Sc, Y, and Zr. This indicates that the rim sequences did not crystallize from the same liquid of the CAI, but condensed from a common gas reservoir with a distinct superrefractory REE signature. Melilite contains excess ^26Mg* with an inferred initial ^26Al/^27Al ratio of (4.4 x 10^-5). However, the Mg-Al system in the anorthites of the captured sinuous fragments and the rim layers of the small CAIs is disturbed. This strongly suggests that oxidation and alteration processes took place in the earliest stage of the solar system.

  7. Rees, Sir Martin John (1942-)

    NASA Astrophysics Data System (ADS)

    Murdin, P.

    2000-11-01

    British cosmologist, became Plumian Professor of Astronomy at Cambridge and in 1995 Astronomer Royal (an honorary office by then separated from the directorship of the Royal Observatory at Greenwich). His forte is to be able to model any astrophysical phenomenon with physical insight, and he has successfully applied this technique to quasars, x-ray sources, gamma ray bursters, galaxy formation, g...

  8. Metasomatic enrichment of Proterozoic mantle south of the Kaapvaal Craton, South Africa: origin of sinusoidal REE patterns in clinopyroxene and garnet

    NASA Astrophysics Data System (ADS)

    le Roex, Anton; Class, Cornelia

    2016-02-01

    Xenoliths of mantle peridotite have been sampled from four kimberlite intrusions, Melton Wold, Hebron, Uintjiesberg and Markt, emplaced through the Mesoproterozoic Namaqua-Natal Belt, along the southern border of the Kaapvaal Craton. Although many of the xenoliths are heavily altered, constituent clinopyroxene, garnet and phlogopite are fresh and have been analysed by electron microprobe for major elements and by laser ablation ICP-MS for trace elements. Primitive mantle-normalised REE abundances in clinopyroxene are all strongly LREE enriched and show a range of patterns including uniformly MREE-HREE sloped (referred to here as `normal'), sinusoidal and humped sinusoidal patterns. HREE abundances are extremely low (Yb = 0.3-0.06 × PM). REEN patterns in coexisting garnets show a similar range of patterns. When normalised to primitive mantle values, trace element patterns in some clinopyroxenes show strong relative depletion in Rb-Ba, Ta-Nb and Ti, with some samples also being relatively depleted in Zr-Hf. These trace element characteristics are indistinguishable from those found in clinopyroxene and garnet from peridotites from the adjacent cratonic mantle. Numerical modelling of reactive porous flow of an enriched metasomatic melt through a geochemically depleted peridotite matrix can account for the full range in observed REEN patterns. The relative depletion in Rb-Ba, Ta-Nb and Ti can be accounted for by an early crystallisation of phlogopite from the percolating melt. The relative depletion in Zr-Hf in some clinopyroxenes requires either zircon to crystallise in the proximal metasomatic assemblage, or metasomatism by a carbonatitic melt. Modelling results, together with the absence of clinopyroxene with depleted or even partially enriched REEN patterns, suggest that all clinopyroxene has been modally introduced through metasomatism into an initially highly depleted harzburgitic protolith. The range in Sr and Pb isotopic composition of the clinopyroxenes

  9. Biodegradation of the french reference nuclear glass SON 68 by Acidithiobacillus thiooxidans : protective effect of the biofilm,U and REE retention

    NASA Astrophysics Data System (ADS)

    Bachelet, M.; Crovisier, J.; Stille, P.; Boutin, R.; Vuilleumier, S.; Geoffroy, V.

    2008-12-01

    Although underground nuclear waste repositories are not expected to be favourable places for microbial activity, one should not exclude localized action of extremophilic bacteria on some materials involved in the storage concept. Among endogenous or accidentally introduced acidophiles, some are susceptible to lead to a locally drastic decreased in pH with potential consequences on materials corrosion. Experiments were performed with Acidithiobacillus thiooxidans on 100-125 μm french reference nuclear glass SON68 grains in a mineral medium under static conditions during 60 days at 25°C. Growth medium was periodically renewed and analyzed by ICP-AES and ICP-MS spectrometry for both major, traces and ultra-traces elements. Biofilm formation was evidenced by confocal laser microscopy, staining DNA with ethidium bromide and exopolysaccharides with calcofluor white. Biofilm thickness around material grains exceeded 20 μm under the chosen experimental conditions. It can be noticed that while numerous studies on biofilm formation upon interaction between Acidithiobacillus ferrooxidans and materials can be found in the literature, evidence for biofilm formation is still scarce for the case of the acidophilic bacterium A. thiooxidans. Presence of biofilm is a key parameter for material alteration at the solid/solution interface in biotic systems. Indeed, various constitutive elements of materials trapped in the polyanionic polymer of biofilm may also influence the alteration process. In particular, biofilm may reduce the alteration rate of materials by forming a protective barrier at their surface (Aouad et al., 2008). In this study, glass alteration rates, determined using strontium, molybdenum and caesium as tracers, showed that the biofilm has a protective effect against glass alteration. U and REE are efficiently trapped in the biogenic compartment of the system (exopolysaccharides (EPS) + bacterial cells). Biofilm analysis are in progress to determine whether these

  10. Effect of thermal maturation on the K-Ar, Rb-Sr and REE systematics of an organic-rich New Albany Shale as determined by hydrous pyrolysis

    USGS Publications Warehouse

    Clauer, Norbert; Chaudhuri, Sambhudas; Lewan, M.D.; Toulkeridis, T.

    2006-01-01

    Hydrous-pyrolysis experiments were conducted on an organic-rich Devonian-Mississippian shale, which was also leached by dilute HCl before and after pyrolysis, to identify and quantify the induced chemical and isotopic changes in the rock. The experiments significantly affect the organic-mineral organization, which plays an important role in natural interactions during diagenetic hydrocarbon maturation in source rocks. They produce 10.5% of volatiles and the amount of HCl leachables almost doubles from about 6% to 11%. The Rb-Sr and K-Ar data are significantly modified, but not just by removal of radiogenic 40Ar and 87Sr, as described in many studies of natural samples at similar thermal and hydrous conditions. The determining reactions relate to alteration of the organic matter marked by a significant change in the heavy REEs in the HCl leachate after pyrolysis, underlining the potential effects of acidic fluids in natural environments. Pyrolysis induces also release from organics of some Sr with a very low 87Sr/86Sr ratio, as well as part of U. Both seem to have been volatilised during the experiment, whereas other metals such as Pb, Th and part of U appear to have been transferred from soluble phases into stable (silicate?) components. Increase of the K2O and radiogenic 40Ar contents of the silicate minerals after pyrolysis is explained by removal of other elements that could only be volatilised, as the system remains strictly closed during the experiment. The observed increase in radiogenic 40Ar implies that it was not preferentially released as a volatile gas phase when escaping the altered mineral phases. It had to be re-incorporated into newly-formed soluble phases, which is opposite to the general knowledge about the behavior of Ar in supergene natural environments. Because of the strictly closed-system conditions, hydrous-pyrolysis experiments allow to better identify and even quantify the geochemical aspects of organic-inorganic interactions, such as

  11. Paleoenvironments in Meso-Neoproterozoic carbonates of the Mbuji-Mayi Supergroup (Democratic Republic of Congo) - Microfacies analysis combined with C-O-Sr isotopes, major-trace elements and REE + Y distributions

    NASA Astrophysics Data System (ADS)

    Delpomdor, F.; Blanpied, C.; Virgone, A.; Préat, A.

    2013-12-01

    The Meso- and Neoproterozoic Mbuji-Mayi Supergroup (1155 Ma to ca. 800 Ma) was deposited in the SE-NW trending siliciclastic-carbonate failed-rift in the Sankuru-Mbuji-Mayi-Lomami-Lovoy Basin. Drillcore- and outcrop-derived microfacies, isotope (C, O and Sr) compositions of carbonates and REE + Y distributions are integrated to unravel the paleoenvironmental and chemical conditions prevailing during deposition and alteration (or contamination) of the Mbuji-Mayi carbonates. The carbonate succession (BIe subgroup and BIIa to BIIe subgroups), composed of 11 microfacies (MF), records the evolution of a marine ramp submitted to evaporation, with basinal and low-energy outer-ramp environments (MF1-MF5), biohermal mid-ramp (MF6) and restricted tide-dominated lagoon inner-ramp (MF7-MF9) settings, overlain by lacustrine (MF10) and sabkha (MF11) environments. The ramp margin is characterized by thick stacks of stromatolitic bioherms. δ13C and δ18O relationships in the Mbuji-Mayi carbonates allow discrimination between meteoric (δ13C: -7.5‰ to +0.0‰, δ18O: -7.0‰ to -1.0‰) and burial lithifications (δ13C: -1.5‰ to +0.0‰, δ18O: -15.1‰ to -7.0‰), that overprinted a primary marine signal (δ13C: -1.5‰ to +2.0‰, δ18O: -3.0‰ to +0.5‰) partially preserved in the subgroups. Unaltered pristine signals are found in the Mbuji-Mayi carbonates with 87Sr/86Sr ratios (0.7065-0.7082) similar to those of the marine-preserved strontium signatures of the early Neoproterozoic oceans. The PAAS-normalized REE + Y distributions indicate that the BIe carbonates were altered by Fe-oxide-rich hydrothermal fluids. BIIb and BIIe carbonates exhibit uniform light REE depleted patterns suggesting inputs of detrital river material whereas a marine seawater, highlighted by the REE + Y distributions is preserved in BIIc and BIId carbonates. The pattern of carbon, oxygen and strontium isotopic variations in the Mbuji-Mayi carbonates reflects deposition and early diagenesis in

  12. Structure-related geochemical (REE) and isotopic (K-Ar, Rb-Sr, {delta}{sup 18}O) characteristics of clay minerals from Rotliegend sandstone reservoirs (Permian, northern Germany)

    SciTech Connect

    Zwingmann, H.; Clauer, N.; Gaupp, R.

    1999-09-01

    Euhedral illite cementing the gas-bearing sandstone reservoirs of the Rotliegend in the Niedersaechsische rift system (northern Germany) was studied along a horst-to-graben cross-section to examine its chemical and isotopic characteristics. The data show that differentiated illite particles grew during a tectono-thermal event marked by distinct episodic hydrothermal activities along fault drains and in the poral space of sandstones at 210 Ma and at 195 to 190 Ma in horst positions, at 185 to 175 Ma in the nearby graben, and at 170 to 165 Ma in both the horst and graben. Varied REE distribution patterns and initial {sup 87}Sr/{sup 86}Sr ratios (from 0.7124 to 0.7142) relative to illite-particle size outline a high chemical variability of the fluids during illite growth. The {delta}{sup 18}O values of illite range from +20.0 to +12.4% and those of chlorite from +12.0 to +6.9%. The changing {delta}{sup 18}O values of the minerals most likely relate to varied {delta}{sup 18}O values of the fluids, or to different water/rock ratios during crystallization. Differences among the REE and {sup 87}Sr/{sup 86}Sr tracers and the {delta}{sup 18}O values of different generations of illite also suggest a changing fluid chemistry relative to time. significant positive Eu anomalies and negative Ce anomalies in the REE distributions of illite suggest feldspar alteration by the migrating fluids in oxidizing environments.

  13. Evaluation of carbonate diagenesis: A comparative study of minor elements, trace elements, and rare-earth elements (REE + Y) between Pleistocene corals and matrices from Grand Cayman, British West Indies

    NASA Astrophysics Data System (ADS)

    Li, Rong; Jones, Brian

    2014-12-01

    On Grand Cayman, the Pleistocene Ironshore Formation consists of six unconformity-bounded units of limestones that have been partially or completely altered to calcite by post-depositional meteoric diagenesis. In order to examine the diagenetic history from the perspective of geochemical elements, the concentrations of minor element (Sr, Na, Mg), trace elements (Ba, Fe, Mn, Al, Si), and rare-earth elements (REE) and yttrium (Y) were determined for 105 corals and 84 matrices collected from the Rogers Wreck Point (RWP), Western Onshore area (WO), and offshore George Town (GT) areas. With the transformation of aragonite to calcite, the Sr, Na, and Ba values decreased, but Mg increased, which are indicative of diagenetic alteration in an open water system. Due to intrinsic "vital effects" and the extrinsic diagenetic environment, the variations of Sr, Na, Ba, and Mg concentrations between Acropora and Montastrea from the GT area are different to those of their counterparts from RWP and WO. The signatures of Sr, Na, Ba, and Mg are in good agreement with the diagenetic history as determined from petrographic and stable isotopic criteria. The REE + Y (REY) concentrations (ΣREY) are higher in the matrices (0.2-6.9 ppm, average 2.6 ppm) than in the associated corals (0.1-5.4 ppm, average 0.6 ppm). Shale-normalized REY patterns of the Pleistocene Ironshore Formation are similar to those of oxygenated seawater, which are characterized by (1) light REE depletion relative to heavy REE (average DySN/SmSN = 1.7, n = 35), (2) positive La anomalies (average Pr/Pr* = 1.17, n = 53), and (3) negative Ce anomalies (average Ce/Ce* = 0.49, n = 53). The preserved seawater-like REY distribution pattern, the lack of correlation between ΣREY and mineralogy, and the lack of correlation between ΣREY and diagenesis-sensitive stable oxygen isotope (δ18O) indicate that meteoric diagenesis did not have a major impact on the REY distribution patterns. The matrices and corals in the GT area

  14. Petrographic, REE, fluid inclusion and stable isotope study of magnesite from the Upper Triassic Burano Evaporites (Secchia Valley, northern Apennines): contributions from sedimentary, hydrothermal and metasomatic sources

    NASA Astrophysics Data System (ADS)

    Lugli, Stefano; Morteani, Giulio; Blamart, Dominique

    2002-06-01

    Sparry and microcrystalline magnesite are minor constituents of the Upper Triassic Burano Evaporite Formation of the northern Apennines in Italy. Petrography and geochemistry of magnesite suggest three modes of formation. (1) Evaporitic precipitation of stratified microcrystalline magnesite layers associated with sulfate and carbonate rocks. Most REE are below ICP-MS detection limits. δ18O is +20.2‰ (SMOW) and δ13C is -2.6‰ (PDB). (2) Hydrothermal infill of Fe-rich (9.78 wt% FeO) lenticular sparry magnesite. This type of magnesite is characterized by very low LREE concentrations, whereas HREEs are relatively high. The fluid inclusion composition is NaCl-MgCl2-H2O, salinity is ~30 wt% NaCl equiv., and total homogenization temperatures range from 204-309 °C; δ18O is +17.5‰ and δ13C is +1‰. (3) The partial or total replacement of dolostones by lenticular sparry magnesite. LREEs are lower in magnesite compared with the partly replaced dolostones. Magnesite yields δ18O and δ13C compositions of +17.3 to +23.6‰ and +0.5 to +1.4‰, respectively, whereas the partly replaced dolostones yield δ18O and δ13C values of +25.0 to +26.2 and +1.3 to +1.9, respectively. Complete replacement of dolostones produced massive lenticular sparry magnesite rock containing ooids and axe-head anhydrite relicts; LREEs are depleted compared to unaffected dolostones; δ18O and δ13C compositions range from +16.4 to +18.4‰ and +0.4 to +0.9‰, respectively. These data and the association between fracture-filling and replacive magnesite suggests a metasomatic system induced by hydrothermal circulation of hot and saline Mg-rich fluids. These processes probably occurred in the Oligocene-Miocene, when the Burano Formation acted as main detachment horizon for the Tuscan Nappe during the greenschist facies metamorphism of the Apuane complex. Thrusting over the Apuane zone produced large scale fluid flow focused at the Tuscan Nappe front. Sources of Mg-rich fluids were metamorphic

  15. Simulations of Diffusive Pb-, Ti- and REE-loss in Terrestrial and Lunar Zircon and Apatite as a Function of Impact Heating During Impact Bombardments

    NASA Astrophysics Data System (ADS)

    Abramov, O.; Mojzsis, S. J.

    2009-12-01

    ejecta following basin-forming impacts. Several parameters were tested, including LHB duration (10 and 100 Myr) and mass delivered (2 × 1020 to 2 × 1021 kg for Earth; 1019 to 1020 kg for the Moon). Models were populated with zircon and apatite grains, and the cumulative distance of cation diffusion as a result of thermal pulses during bombardment was recorded for each grain. Results will be presented as mean Pb-, Ti-, and REE-loss as a function of crustal depth for zircon and apatite grains of diameters 1-100 µm. High degrees of Pb-loss (up to 100%) occur in zircons emplaced on the surface and decrease rapidly with depth. On average, small (10 µm) zircons at 1 km depth would experience 80% Pb-loss, whereas at 5 km, they experience 50% Pb-loss. Apatites lose lead far more readily and are easily reset by impacts. A 10 µm zircon grain reaches open system conditions for Pb at 1200 °C for 1 y, but a 10 µm apatite is reset at only 625 °C. A 10 µm apatite grain is reset in 1 s at ~1750 °C, which is typical in ejectas produced by large impacts. These models explain the apparent absence of an LHB signal so far for lunar zircons using conventional spot analyses, as well as the complete re-setting of Pb ages in lunar apatites for the same rock.

  16. Major and trace (including REEs) element stratigraphy in the first 90 m (around 1 Myr) of ANDRILL AND-1B drillcore.

    NASA Astrophysics Data System (ADS)

    Rugi, Francesco; Becagli, Silvia; Ghedini, Costanza; Severi, Mirko; Traversi, Rita; Udisti, Roberto; Monien, Donata; Kuhn, Gerhard; Giorgetti, Giovanna; Talarico, Franco

    2010-05-01

    An integrated system Inductively Coupled Plasma - Sector Field Mass Spectrometry (ICP-SFMS) and Inductively Coupled Plasma - Atomic Emission Spectrophotometry (ICP - AES) has been applied to quantify 39 major and trace elements (including Rare Earths Elements -REE) in Antarctic glaciomarine sediments collected in the framework of ANDRILL. This project aims to study the role of the Antarctic Continent within the global climatic system, by the recovery and analysis of two deep sediment cores (AND-1B, MIS and AND-2A, SMS), drilled close to the margin of the Ross Ice Shelf. The main goals of ANDRILL were to obtain a stratigraphic record that documents key steps in Antarctica's Cenozoic climatic and glacial history, and in the tectonic evolution of the Transantarctic Mountains and the West Antarctic rift System. In particular, the study of the geochemical composition of sediments along the two ANDRILL cores can provide information about the possible source of terrigenous material deposited over the drilling site (Harwood et al., 2006). Preliminary results with a spatial resolution of about 1 m for the geochemical composition of the interval 24.66- 85.24 m of depth of marine sediments from AND-1B core covering about the last 1 Ma, are here shown. The concentration ratio of each measured element with respect to Al concentration, used as terrigenous reference, was calculated in order to remove the possible effect on elemental concentrations of differences in average sediment grain-size along the core and possible dilution effects and point out specified metal enrichments. The presented data and depth profiles (e.g. Fe/Al, Mn/Al, Co/Al, Cr/Al, Eu/Al and Europium anomaly) relative to sediments deposited during the last Ma at the MIS site, show an evident discontinuity from samples collected above and below 58.4 m of depth, corresponding to about 0.45 Ma BP, following the latest AND-1B dating model (85.24 m of depth corresponding to about 0.988 Ma; the chronological datum of

  17. In situ Sr isotope analysis of apatite by LA-MC-ICPMS: constraints on the evolution of ore fluids of the Yinachang Fe-Cu-REE deposit, Southwest China

    NASA Astrophysics Data System (ADS)

    Zhao, Xin-Fu; Zhou, Mei-Fu; Gao, Jian-Feng; Li, Xiao-Chun; Li, Jian-Wei

    2015-10-01

    Apatite is a ubiquitous accessory mineral in a variety of rocks and hydrothermal ores. Strontium isotopes of apatite are well known to retain petrogenetic information and have been widely used to investigate the origin of igneous rocks, but such attempts have rarely been made to constrain ore-forming processes of hydrothermal systems. We here report in situ LA-MC-ICPMS Sr isotope data of apatite from the ~1660-Ma Yinachang Fe-Cu-REE deposit, Southwest China. The formation of this deposit was coeval to the emplacement of regionally distributed doleritic intrusions within a continental-rift setting. The deposit has a paragenetic sequence consisting of sodic alteration (stage I), magnetite mineralization (stage II), Cu sulfide and REE mineralization (stage III), and final barren calcite veining (stage IV). The stage II and III assemblages contain abundant apatite, allowing to investigate the temporal evolution of the Sr isotopic composition of the ore fluids. Apatite of stage II (Apt II) is associated with fluorite, magnetite, and siderite, whereas apatite from stage III (Apt III) occurs intimately intergrown with ankerite and Cu sulfides. Apt II has 87Sr/86Sr ratios varying from 0.70377 to 0.71074, broadly compatible with the coeval doleritic intrusions (0.70592 to 0.70692), indicating that ore-forming fluids responsible for stage II magnetite mineralization were largely equilibrated with mantle-derived mafic rocks. In contrast, Apt III has distinctly higher 87Sr/86Sr ratios from 0.71021 to 0.72114, which are interpreted to reflect external radiogenic Sr, likely derived from the Paleoproterozoic strata. Some Apt III crystals have undergone extensive metasomatism indicated by abundant monazite inclusions. The metasomatized apatite has much higher 87Sr/86Sr ratios up to 0.73721, which is consistent with bulk-rock Rb-Sr isotope analyses of Cu ores with 87Sr/86Sri from 0.71906 to 0.74632. The elevated 87Sr/86Sr values of metasomatized apatite and bulk Cu ores indicate

  18. Fluid sources and metallogenesis in the Blackbird Co-Cu-Au-Bi-Y-REE district, Idaho, U.S.A.: Insights from major-element and boron isotopic compositions of tourmaline

    USGS Publications Warehouse

    Trumbull, R.B.; Slack, J.F.; Krienitz, M.-S.; Belkin, H.E.; Wiedenbeck, M.

    2011-01-01

    Tourmaline is a widespread mineral in the Mesoproterozoic Blackbird Co-Cu-Au-Bi-Y-REE district, Idaho, where it occurs in both mineralized zones and wallrocks. We report here major-element and B-isotope compositions of tourmaline from stratabound sulfide deposits and their metasedimentary wallrocks, from mineralized and barren pipes of tourmaline breccia, from late barren quartz veins, and from Mesoproterozoic granite. The tourmalines are aluminous, intermediate in the schorl-dravite series, with Fe/(Fe + Mg) values of 0.30 to 0.85, and 10 to 50% X-site vacancies. Compositional zoning is prominent only in tourmaline from breccias and quartz veins; crystal rims are enriched in Mg, Ca and Ti, and depleted in Fe and Al relative to cores. The chemical composition of tourmaline does not correlate with the presence or absence of mineralization. The ??11B values fall into two groups. Isotopically light tourmaline (-21.7 to-7.6%o) occurs in unmineralized samples from wallrocks, late quartz veins and Mesoproterozoic granite, whereas heavy tourmaline (-6.9 to +3.2%o) is spatially associated with mineralization (stratabound and breccia-hosted), and is also found in barren breccia. At an inferred temperature of 300??C, boron in the hydrothermal fluid associated with mineralization had ??11B values of-3 to +7%o. The high end of this range indicates a marine source of the boron. A likely scenario involves leaching of boron principally from marine carbonate beds or B-bearing evaporites in Mesoproterozoic strata of the region. The ??11B values of the isotopically light tourmaline in the sulfide deposits are attributed to recrystallization during Cretaceous metamorphism, superimposed on a light boron component derived from footwall siliciclastic sediments (e.g., marine clays) during Mesoproterozoic mineralization, and possibly a minor component of light boron from a magmatic-hydrothermal fluid. The metal association of Bi-Be-Y-REE in the Blackbird ores suggests some magmatic input

  19. REE, Y, Nb, U, and Th contents and tetrad effect in zircon from a magmatic-hydrothermal F-rich system of Sn-rare metal-cryolite mineralized granites from the Pitinga Mine, Amazonia, Brazil

    NASA Astrophysics Data System (ADS)

    Nardi, Lauro V. S.; Formoso, Milton L. L.; Jarvis, Kym; Oliveira, Leondres; Bastos Neto, Artur C.; Fontana, Eduardo

    2012-02-01

    The geochemistry of zircon from the granites that host the Sn-Rare-Metal-cryolite deposit of Pitinga Mine in northern Brazil, Amazonia, is discussed based on data obtained by LA-ICP-MS. The ore deposit is one of the largest in the world and is related with F-rich A-type granite intrusions of 1822 ± 2 Ma. REE, Y, U, Th, Nb, Ta, Pb, and Hf contents were determined in zircon grains from the albite-bearing facies that contains the ore deposit and from less evolved facies composed of amphibole-biotite and biotite granites. The trace-element contents of zircon were compared to those of their host rocks and the calculated zircon/rock ratios are like the values of zircon/melt partition coefficients for natural granitic compositions. The concentrations found for all analysed elements are highly variable, even for determinations made in the same grain. However, the average contents and patterns are like those of typical magmatic zircon and can indicate the composition of the melts from which they were crystallized. The interpretation of trace element contents in the zircon grains suggests that: (i) in the albite-bearing facies, zircon crystallized after the volatile phase exsolution and shows typical geochemical features such as: Th/U ratios from 1 to 10, Y/Ho is lower than 20, Sm/Nd ratios are generally higher than 0.5, Nb/Y is higher than 0.08, and Hf is over 2 wt%; (ii) M-type tetrad effects were produced in the REE patterns of most differentiated melts by F-complex stabilization, and were preserved in some zircon grains; (iii) ore deposition in the Pitinga mine initiated in the late stages of magmatic crystallization mainly following resurgent boiling. The trace element contents of zircon are particularly relevant for provenance studies if mineral/melt partition coefficients are taken into account, so that the approximate trace element pattern of their igneous source can be estimated. The geochemistry of trace elements in zircon, in spite of the wide range of contents

  20. Origin of the eclogitic clasts with graphite-bearing and graphite-free lithologies in the Northwest Africa 801 (CR2) chondrite: Possible origin from a Moon-sized planetary body inferred from chemistry, oxygen isotopes and REE abundances

    NASA Astrophysics Data System (ADS)

    Hiyagon, H.; Sugiura, N.; Kita, N. T.; Kimura, M.; Morishita, Y.; Takehana, Y.

    2016-08-01

    In order to clarify the origin of the eclogitic clasts found in the NWA801 (CR2) chondrite (Kimura et al., 2013), especially, that of the high pressure and temperature (P-T) condition (∼3 GPa and ∼1000 °C), we conducted ion microprobe analyses of oxygen isotopes and rare earth element (REE) abundances in the clasts. Oxygen isotopic compositions of the graphite-bearing lithology (GBL) and graphite-free lithology (GFL) show a slope ∼0.6 correlation slightly below the CR-CH-CB chondrites field in the O three-isotope-diagram, with a large variation for the former and almost homogeneous composition for the latter. The average REE abundances of the two lithologies show almost unfractionated patterns. Based on these newly obtained data, as well as mineralogical observations, bulk chemistry, and considerations about diffusion timescales for various elements, we discuss in detail the formation history of the clasts. Consistency of the geothermobarometers used by Kimura et al. (2013), suggesting equilibration of various elements among different mineral pairs, provides a strong constraint for the duration of the high P-T condition. We suggest that the high P-T condition lasted 102-103 years. This clearly precludes a shock high pressure (HP) model, and hence, strongly supports a static HP model. A static HP model requires a Moon-sized planetary body of ∼1500 km in radius. Furthermore, it implies two successive violent collisions, first at the formation of the large planetary body, when the clasts were placed its deep interior, and second, at the disruption of the large planetary body, when the clasts were expelled out of the parent body and later on transported to the accretion region of the CR chondrites. We also discuss possible origin of O isotopic variations in GBL, and presence/absence of graphite in GBL/GFL, respectively, in relation to smelting possibly occurred during the igneous process(es) which formed the two lithologies. Finally we present a possible

  1. Zircon U-Pb ages and Sr-Nd-Hf isotopes of the highly fractionated granite with tetrad REE patterns in the Shamai tungsten deposit in eastern Inner Mongolia, China: Implications for the timing of mineralization and ore genesis

    NASA Astrophysics Data System (ADS)

    Jiang, Si-Hong; Bagas, Leon; Hu, Peng; Han, Ning; Chen, Chun-Liang; Liu, Yuan; Kang, Huan

    2016-09-01

    The Shamai tungsten deposit is located in the eastern part of the Central Asian Orogenic Belt (CAOB). Tungsten mineralization is closely related to the emplacement of fine- to medium-grained biotite monzogranite (G1) and porphyritic biotite monzogranite (G2) in the Shamai Granite. NW-trending joints and faults host orebodies in the Shamai Granite and Devonian hornfels. The mineralization is characterized by a basal veinlet zone progressing upwards to a thick vein zone followed by a mixed zone, a veinlet zone, and a thread vein zone at the top. The ore-related alteration typically consists of muscovite, greisen, and hornfels. In order to constrain the timing of the Shamai mineralization and discuss the ore genesis, muscovite Ar-Ar, molybdenite Re-Os, and zircon U-Pb geochronological, geochemical, and Sr-Nd-Hf isotopic studies were completed on the deposit. The U-Pb zircon dating yielded weighted mean ages of 153 ± 1 Ma for G1 and 146 ± 1 Ma for G2. Muscovite from a wolframite-bearing quartz vein yielded an Ar-Ar plateau age of 140 ± 1 Ma, whereas two molybdenite samples yielded identical Re-Os model ages of 137 ± 2 Ma. These two ages are younger than the two monzogranites, suggesting a prolonged magmatic-hydrothermal interaction during tungsten mineralization. Major and trace element geochemistry shows that both G1 and G2 are characterized by high SiO2 and K2O contents, high A/CNK values (1.08-1.40), a spectacular tetrad effect in their REE distribution patterns, and non-CHARAC (charge-and-radius-controlled) trace element behavior. This suggests that both G1 and G2 are highly differentiated peraluminous rocks with strong hydrothermal interaction. The Nd-Hf isotope data for the Shamai Granite (εNd(t) between - 1.9 and + 7.4, ɛHf(t) from 5.2 to 12.8) are largely compatible with the general scenario for much of the Phanerozoic granite emplaced in the CAOB. It is here suggested that the Shamai Granite originated from partial melting of a juvenile lower crust with

  2. Genesis of amethyst geodes in basaltic rocks of the Serra Geral Formation (Ametista do Sul, Rio Grande do Sul, Brazil): a fluid inclusion, REE, oxygen, carbon, and Sr isotope study on basalt, quartz, and calcite

    NASA Astrophysics Data System (ADS)

    Gilg, H. Albert; Morteani, Giulio; Kostitsyn, Yuri; Preinfalk, Christine; Gatter, Istvan; Strieder, Adelir J.

    2003-12-01

    In the Ametista do Sul area, Rio Grande do Sul, Brazil, amethyst-bearing geodes are hosted by a ~40- to 50-m-thick subhorizontal high-Ti basaltic lava flow of the Lower Cretaceous Paraná Continental Flood Basalt Province. The typically spherical cap-shaped, sometimes vertically elongated geodes display an outer rim of celadonite followed inwards by agate and colorless and finally amethystine quartz. Calcite formed throughout the whole crystallization sequence, but most commonly as very late euhedral crystals, sometimes with gypsum, in the central cavity. Fluid inclusions in colorless quartz and amethyst are predominantly monophase and contain an aqueous liquid. Two-phase liquid-vapor inclusions are rare. Some with a consistent degree of fill homogenize into the liquid between 95 and 98 °C. Ice-melting temperatures in the absence of a vapor phase between -4 and +4 °C indicate low salinities. Chondrite-normalized REE patterns of calcites are highly variable and show generally no systematic correlation with the paragenetic sequence. The oxygen isotope composition of calcites is very homogeneous (δ18OVSMOW=24.9±1.1‰, n=34) indicating crystallization temperatures of less than 100 °C. Carbon isotope values of calcites show a considerable variation ranging from -18.7 to -2.9‰ (VPDB). The 87Sr/86Sr ratio of calcites varies between 0.706 and 0.708 and is more radiogenic than that of the host basalt (~0.705). The most likely source of silica, calcium, carbon, and minor elements in the infill of the geodes is the highly reactive interstitial glass of the host basalts leached by gas-poor aqueous solutions of meteoric origin ascending from the locally artesian Botucatú aquifer system in the footwall of the volcanic sequence. The genesis of amethyst geodes in basalts at Ametista do Sul, Brazil, is thus considered as a two-stage process with an early magmatic protogeode formation and a late, low temperature infill of the cavity.

  3. A mantle- and a lower crust-derived bimodal suite in the Yusufeli (Artvin) area, NE Turkey: trace element and REE evidence for subduction-related rift origin of Early Jurassic Demirkent intrusive complex

    NASA Astrophysics Data System (ADS)

    Dokuz, Abdurrahman; Tanyolu, Erkan; Genç, Salim

    2006-06-01

    , unfractionated HREE patterns and evolution towards the higher Y concentrations and lower Sr/Y ratios within the body. All these features are obtained in experimentally produced melts from mafic rocks at low pressures (≤5 kbar) and also widespread in the rocks of arc where old (Upper Cretaceous or older) oceanic crust is being subducted. Major and REE modelling supports formation of the quartz dioritic parent to the felsic intrusive rocks by 70% partial melting of a primitive gabbroic sample (G694). Therefore, once taking into account the extensional conditions prevailing in the Pontian arc crust in Early Jurassic time, former basic products (gabbros) seem to be the most appropriate source for the tonalite-trondhjemite body. Magmatic emplacement of stratigraphically similar lithologies in the Pulur Massif, just southwest of the Yusufeli, was dated to be 184 Ma by the 40Ar/39Ar method on amphibole, and is compatible with the initiation of Early Jurassic rifting in the region.

  4. The origin of fluids and the effects of metamorphism on the primary chemical compositions of Barberton komatiites: New evidence from geochemical (REE) and isotopic (Nd, O, H, 39Ar /40Ar ) data

    NASA Astrophysics Data System (ADS)

    Lécuyer, C.; gruau, G.; Anhaeusser, C. R.; Fourcade, S.

    1994-01-01

    Numerous greenstone relics, all containing the two lowermost formations of the Onverwacht Group, occur in the Archean trondhjemitic/tonalitic gneiss terrains south of the Barberton Greenstone Belt. In this study, we report detailed petrological, geochemical and isotopic (Nd, O, H, 40Ar /39Ar ) data obtained on komatiites from the Schapenburg Greenstone Remnant (SGR), the largest and best-preserved greenstone relic. The main goals are (1) to date the metamorphism affecting the SGR using the 40Ar /39Ar dating method on amphiboles, (2) to evaluate the effect of metamorphism on the preservation of primary isotopic and chemical signatures, (3) to estimate the temperature and water/rock ratios that prevailed during metamorphic recrystallization in order to constrain the composition and origin of the reacting fluid phase. 40Ar /39Ar ages of 2.9 Ga obtained on two amphibole separates from the Schapenburg metavolcanics reveal the existence of a metamorphic event younger than the emplacement age (3.5 Ga). This metamorphic event belongs to a series of discrete periods of thermal activity from 3.4 to 2 Ga, each of which coincides with a major episode of magmatic activity. The ultrabasic lava flows acquired their δ 18O values (from +3.2 to +5%.) at high temperature (≈450°C) under high water/rock ratios. The reacting water had initial isotopic values typical of metamorphic fluids ( δ18O = +5 to +7%.; δD = -65 to -50%.). REE patterns were not disturbed by metamorphic recrystallization. Despite the long time interval between emplacement and metamorphism (≈600 Ma), ɛNd( T) values are uniform throughout the whole magmatic suite, indicating that the Sm-Nd system was closed on the sample scale during metamorphism. The mantle source of these greenstones was depleted in LREE as evidence by ɛNd( T) ≈ +2.5. Chemical fluxes during metamorphism were calculated for elements unfractionated by olivine removal (e.g. Na, Ca, Ti, Al, and Sr), by normalizing to Nd. They suggest a

  5. Menzerite-(Y) a New Species {(Y REE)(Ca Fe2plus)2}[(Mg Fe2plus)(Fe3plus Al)](Si3)O12 from a Felsic Granulite Parry Sound Ontario and a New Garnet End-member (Y2Ca)Mg2(SiO4)3

    SciTech Connect

    E Grew; J Marsh; M Yates; B Lazic; T Armbruster; A Locock; S Bell; M Dyar; H Bernhardt; O Medenbach

    2011-12-31

    Menzerite-(Y), a new mineral species, forms reddish brown cores, n = 1.844 (20), up to 70 {micro}m across, rimmed successively by euhedral almandine containing up to 2.7 wt% Y{sub 2}O{sub 3} and by K-feldspar in a felsic granulite on Bonnet Island in the interior Parry Sound domain, Grenville Orogenic Province, Canada. It is named after Georg Menzer (1897-1989), the German crystallographer who solved the crystal structure of garnet. Single-crystal X-ray-diffraction results yielded space group Ia3d, a = 11.9947(6) {angstrom}. An electron-microprobe analysis of the grain richest in Y (16.93 wt% Y{sub 2}O{sub 3}) gave the following formula, normalized to eight cations and 12 oxygen atoms: {l_brace}Y{sub 0.83}Gd{sub 0.01}Dy{sub 0.05}Ho{sub 0.02}Er{sub 0.07}Tm{sub 0.01}Yb{sub 0.06}Lu{sub 0.02}Ca{sub 1.37}Fe{sub 0.49}{sup 2+}Mn{sub 0.07}{r_brace} [Mg{sub 0.55}Fe{sub 0.42}{sup 2+}Fe{sub 0.58}{sup 3+}Al{sub 0.35} V{sub 0.01}Sc{sub 0.01}Ti{sub 0.08}](Si{sub 2.82}Al{sub 0.18})O{sub 12}, or {l_brace}(Y,REE)(Ca,Fe{sup 2+}){sub 2}{r_brace}[(Mg,Fe{sup 2+})(Fe{sup 3+},Al)](Si{sub 3})O{sub 12}. Synchrotron micro-XANES data gave Fe{sup 3+}/{Sigma}Fe = 0.56(10) versus 0.39(2) calculated from stoichiometry. The scattering power refined at the octahedral Y site, 17.68 epfu, indicates that a relatively light element contributes to its occupancy. Magnesium, as determined by electron-microprobe analyses, would be a proper candidate. In addition, considering the complex occupancy of this site, the average Y-O bond length of 2.0244(16) {angstrom} is in accord with a partial occupancy by Mg. The dominance of divalent cations with Mg > Fe{sup 2+} and the absence of Si at the octahedral Y site (in square brackets) are the primary criteria for distinguishing menzerite-(Y) from other silicate garnet species; the menzerite-(Y) end-member is {l_brace}Y{sub 2}Ca{r_brace}[Mg{sub 2}](Si{sub 3})O{sub 12}. The contacts of menzerite-(Y) with almandine are generally sharp and, in places, cuspate. It is

  6. Th-REE- and Nb-Ta-accessory minerals in post-collisional Ediacaran felsic rocks from the Katerina Ring Complex (S. Sinai, Egypt): An assessment for the fractionation of Y/Nb, Th/Nb, La/Nb and Ce/Pb in highly evolved A-type granites

    NASA Astrophysics Data System (ADS)

    Moreno, J. A.; Molina, J. F.; Bea, F.; Abu Anbar, M.; Montero, P.

    2016-08-01

    The relationships of Y/Nb, Th/Nb, La/Nb and Ce/Pb ratios in A-type felsic rocks from the Ediacaran Katerina Ring Complex, northernmost Arabian-Nubian Shield (ANS; S. Sinai, Egypt), are investigated in this work to understand their behavior during generation of highly evolved granitic magmas and to explore the nature of magma sources. Textural and compositional relationships of cognate Th-REE- and Nb-Ta-accessory minerals in Katerina felsic rocks show that chevkinite-group minerals (CGM), monazite, thorite, allanite and xenotime formed from residual liquids in quartz syenite porphyries, quartz monzonites and peralkaline granites, whereas in aluminous granites, allanite and monazite crystallized early, and thorite and columbite formed from residual liquids. Relationships of Y/Nb, Th/Nb, La/Nb and Ce/Pb ratios with Zr/Hf ratios in the aluminous granites and with Be abundances in the peralkaline granites suggest a decrease in La/Nb and Ce/Pb ratios in the former, and in Y/Nb and La/Nb ratios in the latter with crystallization progress. This contrasts with absence of systematic variations of Th/Nb and Ce/Pb ratios in the peralkaline compositions and of Y/Nb ratio in the aluminous ones. In this latter, Th/Nb ratio can present a significant decrease only in highly evolved compositions. An analysis of Y/Nb, Th/Nb, La/Nb and Ce/Pb relationships in worldwide OIB and subduction-related magmatic suites reveals that A-type felsic rocks with (Th/Nb)N < 1.3, (La/Nb)N < 1.3, and (Ce/Pb)N > 1 may have A1-type affinity, and those with (Th/Nb)N > 2, (La/Nb)N > 2, and (Ce/Pb)N < 1 tend to present A2-type affinity. The crystal fractionation of Th-LREE- and Nb-Ta-accessory minerals and mixing of components derived from the two granite groups may cause deviations from these compositional limits that can be evaluated using constraints imposed by Th/Nb-La/Nb, Ce/Pb-Th/Nb and Ce/Pb-La/Nb relationships in OIB and subduction-related magmatic suites. Three mantle sources might have been

  7. Chemical Characteristic of CK Chondrites in the Light of P, REEs, Th, and U

    NASA Astrophysics Data System (ADS)

    Ebihara, M.; Shirai, N.; Takahashi, H.

    2015-07-01

    A total of 16 Antarctic CK chondrites were analyzed by ICP-AES for P and by ICP-MS for rare earth elements, Th and U. Based on the data for these elements, the formation process and the structure of CK chondrite parent body are discussed.

  8. The distribution of Sr and REE between diopside and silicate liquid. [Rare Earth Elements

    NASA Technical Reports Server (NTRS)

    Grutzeck, M.; Kridelbaugh, S.; Weill, D.

    1974-01-01

    Experimental determination of the distribution coefficients in diopside-liquid pairs for strontium and nine rare-earth elements in the system CaMgSi2O6-NaAlSi3O8-CaAl2Si2O8. In experiments in air at 1265 C it is found that most of the Sr(2+), Eu(2+), and RE(3+) ions substitute for Ca(2+) and, in addition, a coupled substitution of Al(3+) for Si(4+) occurs. All of the trace ions considered are found to be excluded from the diopside lattice relative to the liquid. In the case of the trivalent ions the exclusion is much more pronounced for La and Ce, which have ionic radii larger than that of Ca(2+) in 8-fold oxygen coordination. Divalent Sr and Eu with even larger radii are also strongly excluded.

  9. Effect of Titanium on REE and HFSE Partitioning Between Garnet and Melt

    NASA Astrophysics Data System (ADS)

    Dwarzski, R. E.; Draper, D. S.

    2004-12-01

    Garnet is a strong fractionator of trace elements and plays an important role in the petrogenetic history of planetary interiors at high pressure. In order to model petrogenetic processes that operate within terrestrial planets accurately, it is important to understand how garnet partitions rare earth and high field strength elements. Here we assess the influence of Ti on garnet-melt trace element partitioning with a view both to constrain important crystal-chemical effects and to evaluate possible roles for garnet in lunar petrogenesis. Experiments were performed at ˜5 GPa and 1650-1675° C in a Walker-style multi-anvil high pressure apparatus using an Apollo 14 black picritic glass composition ( ˜17 wt% TiO2) to assess the effect of Ti on garnet partitioning. These experiments were also designed to examine the possible presence of garnet in mare source regions. Experimental charges were analyzed for major and trace elements by EPMA and SIMS, respectively. D-values measured in this study using the Apollo 14 black Ti-rich composition are consistently higher than those measured by Draper et al. (2004, LPSC XXXV:1297), who used Apollo 15 green C glass (<0.5 wt% TiO2). D vs. ionic radii are well-described for the trivalent cations by the lattice-strain partitioning model of Blundy and Wood (1994, Nature 372:452), with D0 = 2.27 ± 0.40, E = 159 ± 58 GPa, and r0 = 0.879 ± 0.044 Å (r2 = 0.957). For comparison, this model applied to the low-Ti experiments of Draper et al. (2004) yields D0 = 2.93 ± 0.25, E = 572 ± 40 GPa, and r0 = 0.926 ± 0.005 Å (r2 = 0.996) at ˜3.5 GPa. Both these fits show significant mismatch to the partitioning predicted by the formulations of van Westrenen et al. (2001, CMP 142:219), as previously shown for Fe-rich systems by Draper et al. (2003, PEPI 139:149). Use of our D-values (for rare earth and high field strength elements in batch-melting models) provisionally supports the hypotheses of Neal (2001, JGR 106:27865) and Neal and Shearer (2004, LPSC XXXV:2135), who proposed that garnet was present in the source regions of lunar mare basalts. The results of these calculations are similar to those using data from garnet-melt partitioning in very Ti-poor systems (Draper et al. 2004).

  10. Fluid inclusion and stable isotope data for the Pea Ridge Fe-REE orebody, Missouri

    SciTech Connect

    Sidder, G.B.; Day, W.C.; Rye, R.O. )

    1993-03-01

    New fluid-inclusion and stable-isotope data define the character of the mineralizing fluids that formed the iron and rare-earth-element ore deposit at the Pea Ridge Mine, southeast Missouri. These fluids were very hot and highly saline brines that may have been magmatically derived. Early, pre-magnetite ore skarn alteration of the host rhyolitic tuff took place at temperatures greater than 420 C and possibly as high as 680 C based upon calculated temperatures of quartz-magnetite pairs. Halite homogenization of three- or more phase (liquid + vapor + salts) fluid inclusions in quartz indicates that the skarn-forming fluid had a temperature of about 460 C to > 530 C and a salinity of about 45 to 57 equivalent weight percent NaCl. Analyses of [delta][sup 18]O in quartz from the skarn zone average about 14.5[per thousand], compared to a value of about 13.0[per thousand] for quartz in the host rhyolite. Average [delta][sup 34]S values for pyrite of about 2.3[per thousand] in the skarn zone may reflect a magmatic source. Magnetite ore was deposited at temperatures between about 340 C and 530 C from a fluid with a salinity between about 54 and 60 equivalent weight percent NaCl. The large apparent range of temperatures indicated by both fluid-inclusion and stable-isotope data within each zone may be due to contamination by quartz from multiple stages of quartz deposition. Also, the assumed isotopic equilibrium between some mineral pairs may be incorrect. Moreover, fluid inclusions are relatively rare in all ore and alteration zones except the silicified zone, and only a few inclusions are clearly primary in origin. Nonetheless, the predominance of high temperatures and high salinities in all of the mineralized and altered zones supports the interpretation that Pea ridge is a magmatic hydrothermal deposit. This magmatic hydrothermal model is also supported by paragenetic relations defined by geologic mapping and geochemical modeling of major-, minor-, and trace-element data.

  11. Using Rare Earth Elements (REE) to determine wind-driven soil dispersal from a point source

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Although erosion of soil by water is a predictably directional process, the erosion of soil by wind is determined by wind direction on an event-wise basis. The wind-driven dispersal patterns of chemical constituents including natural soil components and anthropogenic contaminants are not well under...

  12. Electron Probe Microanalysis of REE in Eudialyte Group Minerals: Challenges and Solutions.

    PubMed

    Atanasova, Petya; Krause, Joachim; Möckel, Robert; Osbahr, Inga; Gutzmer, Jens

    2015-10-01

    Accurate quantification of the chemical composition of eudialyte group minerals (EGM) with the electron probe microanalyzer is complicated by both mineralogical and X-ray-specific challenges. These include structural and chemical variability, mutual interferences of X-ray lines, in particular of the rare earth elements, diffusive volatility of light anions and cations, and instability of EGM under the electron beam. A novel analytical approach has been developed to overcome these analytical challenges. The effect of diffusive volatility and beam damage is shown to be minimal when a square of 20×20 µm is scanned with a beam diameter of 6 µm at the fastest possible speed, while measuring elements critical to electron beam exposure early in the measurement sequence. Appropriate reference materials are selected for calibration considering their volatile content and composition, and supplementary offline overlap correction is performed using individual calibration factors. Preliminary results indicate good agreement with data from laser ablation inductively coupled plasma mass spectrometry demonstrating that a quantitative mineral chemical analysis of EGM by electron probe microanalysis is possible once all the parameters mentioned above are accounted for. PMID:26313878

  13. Modeling of temperature fields in the working chamber of the process furnace for REE synthesis

    NASA Astrophysics Data System (ADS)

    Kerbel, B. M.; Yu, Ageev A.; Yu, Payusov A.; Katsnelson, L. M.; Tereshchenko, E. V.; Verkhoturova, V. V.

    2016-02-01

    The results of mathematical modeling of temperature fields in the working chamber of the process furnace for special purposes are shown. Studied laboratory furnace is test equipment, which is used for practicing the stages of the technological process of continuous solid-phase synthesis of nanopowders of various purpose, such as obtaining of luminophore powders with rare earth elements oxides in its composition. Mathematical model adequacy is tested empirically

  14. Tambo Quemado: Extraordinary concentrations of REE and refractory trace elements caused by artificial heating

    NASA Technical Reports Server (NTRS)

    Olsen, E.; Hutcheon, I.; Moore, C.

    1993-01-01

    Buchwald examined samples of the IIIB iron Tambo Quemado (TAMQ) cut from the 130 kg main mass. He determined it had been artificially heated, at some time prior to being reported, in an attempt to obtain metal from it. Although the Widmanstatten structure appears relatively unaffected under macroscopic examination, microscopic study of etched sections reveals the effect of the heating. Taenite and plessite area boundaries are indistinct due to high temperature diffusion. Schreibersite, once present in significant amounts, has been melted. Schreibersites in the interior have resolidified in fine-grained eutectic textures surrounded by dark-etching metal rims supersaturated with phosphorus. Buchwald states that phosphate minerals were probably present originally, because graftonite, and its polymorph sarcopside (both essentially Fe3(PO4)2), are common in irons of the IIIB groups. Based on his metallographic study Buchwald estimates TAMQ was heated to 1000 C for about one hour. An interior sample from TAMQ was examined in order to determine what effect this unintended heating 'experiment' had upon the phosphate phases.

  15. Crystal Structure and Crystal Chemistry of Some Common REE Minerals and Nanpingite

    NASA Astrophysics Data System (ADS)

    Ni, Yunxiang

    1995-01-01

    Part I. Crystal structure and crystal chemistry of fluorocarbonate minerals. The crystal structure of bastnasite-(Ce) have been solved in P-62c and refined to R = 0.018. The structure is composed of (001) (CeF) layers interspersed with (CO_3) layers in a 1:1 ratio. The Ce atom is coordinated in rm CeO_6F_3 polyhedra. The atomic arrangement of synchysite-(Ce) has been solved and refined to R = 0.036 with a monoclinic space group C2/c. It possesses a (001) layer structure, with layers of (Ca) and (CeF) separated by layers of carbonate groups. The layers stack in a manner analogous to C2/c muscovite. Polytypism similar to the micas may exist in synchysite. The crystal structures of cordylite-(Ce) have been solved in P6 _3/mmc and refined to R = 0.023. The structure and chemical formula are different from those deduced by Oftedal. The formula is rm MBaCe_2(CO _3)_4F, where M is rm Na^+, Ca^{2+}_{1/2 }+ O_{1/2}, or any solution. The presence of (NaF) layer in the structure is the key difference from the Oftedal's structure. This redefinition of the chemical formula and crystal structure of cordylite will be proposed to IMA-CNMMN. Part II. Crystal structure and crystal chemistry of monazite-xenotime series. Monazite is monoclinic, P2 _1/n, and xenotime is isostructural with zircon (I4_1/amd). Both atomic arrangements are based on (001) chains of intervening phosphate tetrahedra and RE polyhedra, with a REO_8 polyhedron in xenotime that accommodates HRE (Tb - Lu) and a REO_9 polyhedron in monazite that preferentially incorporates LRE (La - Gd). As the structure "transforms" from xenotime to monazite, the crystallographic properties are comparable along the (001) chains, with structural adjustments of 2.2 A along (010) to accommodate the different size RE atoms. Part III. Crystal structure of nanpingite-2M _2, the Cs end-member of muscovite. The crystal structure of nanpingite has been refined to R = 0.058. Compared to K^+ in muscovite, the largest interlayer Cs^+ in nanpingite increases (001) separation between adjacent 2:1 layers, but has little effect on the dimensions in (001). The existence of rare 2M_2 polytype in nanpingite is attributed to this large layer separation, which minimizes the repulsion of the superimposed (along (001)) basal oxygens in neighboring tetrahedral layers.

  16. Preparation and properties of double borates of scandium and REE of the cerium subgroup

    SciTech Connect

    Magunov, I.R.; Efryushina, N.P.; Voevudskaya, S.V.; Zhikhareva, E.A.; Zhirnova, A.P.

    1986-02-01

    The authors prepare double borates of scandium and cerium subgroup rare earths with the general formula RSc/sub 3/ (BO/sub 3/)/sub 4/ (R = Ce, Pr, Nd, Sm). It has been shown that these compounds have the structure of the carbonate mineral huntite. Their IR and luminescence spectra have been studied.

  17. Correlations Between Surficial Sulfur and a REE Crustal Assimilation Signature in Martian Shergottites

    NASA Technical Reports Server (NTRS)

    Jones, J. H.; Franz, H. B.

    2015-01-01

    Compared to terrestrial basalts, the Martian shergottite meteorites have an extraordinary range of Sr and Nd isotopic signatures. In addition, the S isotopic compositions of many shergottites show evidence of interaction with the Martian surface/ atmosphere through mass-independent isotopic fractionations (MIF, positive, non-zero delta(exp 33)S) that must have originated in the Martian atmosphere, yet ultimately were incorporated into igneous sulfides (AVS - acid-volatile sulfur). These positive delta(exp 33)S signatures are thought to be governed by solar UV photochemical processes. And to the extent that S is bound to Mars and not lost to space from the upper atmosphere, a positive delta(exp 33)S reservoir must be mass balanced by a complementary negative reservoir.

  18. Albitization and redistribution of REE and Y in IOCG systems: Insights from Moonta-Wallaroo, Yorke Peninsula, South Australia

    NASA Astrophysics Data System (ADS)

    Kontonikas-Charos, Alkis; Ciobanu, Cristiana L.; Cook, Nigel J.

    2014-11-01

    Trace element concentrations, particularly rare earth elements and yttrium (REY) in feldspars and accessory minerals, have been determined in a suite of albitized igneous, metasedimentary and metasomatite rocks from the Moonta-Wallaroo district, Olympic Cu-Au Province, South Australia. Results show that changes in REY-fractionation trends and concentrations in feldspars and common accessories are associated with key textures in albite-bearing associations from different lithologies. In granitic rocks, pseudomorphic replacement of pre-existing feldspars is typified by porous albite with cleavage-oriented intergrowths of sericite and pore-attached hematite. These observations are comparable with albitization features of granitic terranes elsewhere. A mineral association (albite-sericite ± chlorite), similar to that from granitoids, is observed as pervasive spots in limestone, inferring prograde skarnoid reactions at low fluid/rock ratio in an impure carbonate. In metasedimentary and metasomatite rocks with comparable Na2O content (~ 5-6 wt.%), fine-grained granoblastic albite suggests growth under high fluid/rock ratios irrespective of lithology. In such cases, albite with the highest REY content (ΣREY ~ 200 ppm) accounts for the entire REY budget, e.g., in albite-biotite-schist with the lowest abundance of accessory minerals. Nanoscale investigation confirms this albite to be a REY carrier (elements incorporated within the crystal lattice); no pore-attached inclusions are observed. In contrast, albite with the lowest REY-concentration (~ 14 ppm) is encountered in the metasomatite. In such rocks, recording the highest ΣREY (~ 1000 ppm) in whole-rock, partitioning of REY is favoured among the abundant accessories (titanite, apatite) and calc-silicates (actinolite, clinozoisite) rather than albite. Comparable low-REY albite is also found in granitoid-derived albitite (Na2O ~ 5 wt.%), in which abundant accessories and discrete REY-minerals formed during albitization account for the high ΣREY content (~ 700 ppm) in whole rock. The role of coupled dissolution-reprecipitation reactions (CDRR) is critical for REY (re)distribution within albitized igneous rocks, where REY-release from early magmatic accessories and/or feldspars assists REY-enrichment into late albite. The presence of abundant nanopore-attached inclusions in plagioclase demonstrates the nanoscale nature of CDRR-driven albitization in granitoids, consistent with published experimental work on altered granites. Such porosity offers sites for REY entrapment seen within discrete REY-minerals in new-formed K-feldspar. Similarly, release and uptake of REY, concurrent with albitization, is seen in formation of coarser REY-minerals (xenotime, bastnäsite, synchysite) during CDRR-driven replacement of accessory Fe-Ti-oxides by symplectites of chlorite and hematite. Based on the differences identified between the albitization pathways in igneous and metasedimentary rocks, we discuss how albitization proceeds via a series of complex fluid-mineral reactions, each involving the redistribution, accumulation and retention of REY. These reactions are critical for defining the endowment and deportment of REY in rocks that have undergone sodic alteration. Contrary to previous models, albitization appears controlled by pH rather than redox conditions. Despite regional differences in local geological environment and alteration style across the Olympic Cu-Au Province, albitization, the initiation of hydrothermal alteration, is a pre-requisite stage for REY-enrichment in Iron-Oxide-Copper-Gold (IOCG) systems. REY distribution patterns in feldspars may thus have value in mineral exploration as criteria enabling alteration associated with mineralization to be distinguished from the regional background. Strong albitization without superposition of later potassic alteration may not, however, be automatically linked to the formation of giant IOCG deposits. Albitization enhances rock permeability and in a strongly faulted structural environment without a suitable trap, hydrothermal fluids may be more readily lost from the system.

  19. SM-ND Age and REE Systematics of Larkman Nunatek 06319: Closed System Fractional Crystallization of a Shergottite Magma

    NASA Technical Reports Server (NTRS)

    Shafer, J. T.; Brandon, A. D.; Lapen T. J.; Righter, M.; Peslier, A. H.

    2010-01-01

    Sm-Nd isotopic data were collected on mineral separates and bulk rock powders of LAR 06319, yielding an age of 180+/-13 Ma (2(sigma)). This age is concordant with the Lu-Hf age (197+/-29 Ma, [1]) determined in conjunction with these data and the Sm-Nd age (190+/-26 Ma) of Shih et al., 2009 [2]. The Sm-Nd data form at statistically significant isochron (Fig. 1) that is controlled largely by leachate-residue pairs (samples with the R suffix are residues after leaching in cold 2N HCl for 10 minutes).

  20. Effect of temperature on REE and TPE sorption by sulfonated cation exchangers from HNO{sub 3} solutions

    SciTech Connect

    Chuveleva, E.A.; Kharitonov, O.V.; Firsova, L.A.

    1995-05-01

    Numerical and experimental data are presented for sorption from HNO{sub 3} solutions on KU-2 sulfonated cation exchanger as a function of temperature. The capacity for Eu at 70{degrees}C for solutions with [H{sup +}] > 1.0 M in the range [Eu] = 0.023-0.0428 M increases by 20-30%. The width of the sorption front significantly decreases at elevated temperature. The calculations are consistent with the observed experimental sorption process.

  1. Coordination Environments of Highly Charged Cations (Ti, Cr, and Light REE's) in Borosilicate Glass/Melts to 1120C

    SciTech Connect

    Farges, Francois; Brown, Gordon E., Jr.; /Stanford U., Geo. Environ Sci. /SLAC, SSRL

    2007-01-02

    The local environments around Ti, Cr, and several light rare-earth elements (La, Ce, and Nd) were investigated by in-situ XANES spectroscopy in a number of complex borosilicate glasses and melts (to 1120 C) that are used for nuclear waste storage. Examination of the high-resolution XANES spectra at the Ti K-edge shows that the average coordination of Ti changes from {approx}5 to {approx}4.5. Cr is dominantly trivalent in the melts studied. However, its average coordination is probably lower in the melt (tetrahedral ?) as revealed by the more intense Cr-K pre-edge feature. Ce also changes its average valence from dominantly +4 to +3.5 upon glass melting. These changes are reversible at T{sub g}, the glass transition temperature ({approx}500-550 C for these glasses). In contrast, the local environments of Nd, Pr, and La are unaffected by melting. Therefore, structural reorganization of these borosilicate glass/melts above T{sub g} is variable, not only in terms of valence (as for Ce) but also speciation (Ti and Cr). Both the ability of B to adopt various coordination geometries (triangular and tetrahedral) and the chemical complexity of the glass/melts explain these changes.

  2. Coordination Environments of Highly Charged Cations (Ti, Cr, and Light REE's) in Borosilicate Glass/Melts to 1120 deg. C

    SciTech Connect

    Farges, Francois; Brown, Gordon E. Jr.

    2007-02-02

    The local environments around Ti, Cr, and several light rare-earth elements (La, Ce, and Nd) were investigated by in-situ XANES spectroscopy in a number of complex borosilicate glasses and melts (to 1120 deg. C) that are used for nuclear waste storage. Examination of the high-resolution XANES spectra at the Ti K-edge shows that the average coordination of Ti changes from {approx}5 to {approx}4.5. Cr is dominantly trivalent in the melts studied. However, its average coordination is probably lower in the melt (tetrahedral ?) as revealed by the more intense Cr-K pre-edge feature. Ce also changes its average valence from dominantly +4 to +3.5 upon glass melting. These changes are reversible at Tg, the glass transition temperature ({approx}500-550 deg. C for these glasses). In contrast, the local environments of Nd, Pr, and La are unaffected by melting. Therefore, structural reorganization of these borosilicate glass/melts above Tg is variable, not only in terms of valence (as for Ce) but also speciation (Ti and Cr). Both the ability of B to adopt various coordination geometries (triangular and tetrahedral) and the chemical complexity of the glass/melts explain these changes.

  3. Using Rare Earth Element (REE) tracers to identify preferential micro-sites of post-fire aeolian erosion

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Plant communities in desert environments are spatially anisotropic and nutrient islands develop below plant canopies that enhance plant growth and reinforce the spatial anisotropy. Catastrophic disturbance that removes the vegetation such as fire or drought can result in the release of the trapped ...

  4. Rydberg-Klein-Rees 1-Sigma-positive potential curve turning points for the isotopes of carbon monoxide

    NASA Technical Reports Server (NTRS)

    Chackerian, C., Jr.; Goorvitch, D.

    1982-01-01

    First order RKR turning points were computed for (C-12)O16, (C-12)O17, (C-13)O16, (C-12)O18, and (C-13)O18 for vibrational levels up to v = 40. These turning points should be useful in the numerical computation of matrix elements of powers of the internuclear separation.

  5. Algoma-type Neoproterozoic BIFs and related marbles in the Seridó Belt (NE Brazil): REE, C, O, Cr and Sr isotope evidence

    NASA Astrophysics Data System (ADS)

    Sial, Alcides N.; Campos, Marcel S.; Gaucher, Claudio; Frei, Robert; Ferreira, Valderez P.; Nascimento, Rielva C.; Pimentel, Marcio M.; Pereira, Natan S.; Rodler, Alexandra

    2015-08-01

    The Jucurutu Formation in the Seridó Belt, northeastern Brazil, encompasses fine-to coarse-grained amphibolite-facies marbles, locally with cross-bedding and stromatolites. Banded iron formations (BIF) at three localities in this belt comprise itabirites (actinolite- or cummingtonite-itabirite and quartz-hematite itabirite) and iron ores, which are overlain by marbles of the Jucurutu Formation. Diamictites of uncertain stratigraphic position in the Seridó Belt exhibit gneiss and quartzite clasts up to 0.6 m long and a fine-grained metapelitic matrix. The C-isotope stratigraphic pathways for the Jucurutu Formation show negative δ13C values at the base of the formation followed upsection by positive values. At the Ferro do Bonito iron Mine, values as low as -12‰ in carbonates just above the contact with underlying BIF are followed by values of ca. -5‰ and by positive values up section (+4 to +10‰). δ13C values for carbonates of the Jucurutu Formation deposited on top of BIFs at the Riacho Fundo, São João do Sabugi, and Serra da Formiga sections are all positive, the contact surfaces between carbonates and BIFs being covered by weathered material. The 87Sr/86Sr values for carbonate rocks of the Jucurutu Formation are mostly in the 0.7074-0.7075 interval, a ratio commonly observed in the late Cryogenian to the early Ediacaran. The studied BIFs exhibit Cr concentrations one magnitude higher than usual and largely unfractionated Cr isotope composition, similar to average magmatic values. They are characterized by δ53Cr values between -0.42 and -0.12‰, by Ce anomalies (Ce/Ce*) ranging from -0.4 to 0.7, by positive Eu anomalies, and by super-chondritic Y/Ho ratios (>20). The combination of geochemical parameters and association with mafic rocks resemble Algoma-type BIFs. These BIFs possibly formed proximally to hydrothermal vents, in anoxic and acidic deep waters, whereby Fe and Cr were leached from mafic or ultramafic rocks. High concentrations of Cr in the BIF with a magmatic inventory isotope composition, together with pronounced positive Eu anomalies, fit a rift depositional scenario, characterized by narrow basins and strong hydrothermal input, in which anoxic (ferruginous) conditions prevailed. This is substantiated by the occurrence of positive Ce anomalies. Their deposition was followed by carbonates which show "normal" Cr concentrations with slightly positively fractionated δ53Cr values. These carbonates may represent post-glacial cap carbonate sequences deposited in an anoxic to slightly oxic shallow marine environment, as suggested by Ce/Ce* versus Pr/Pr* and Ce/Ce* versus Nd cross-relationships.

  6. REE Sorption Study for Media #1 and Media #2 in Brine #1 and #2 at different Liquid to Solid Ratio's at Ambient Temperature

    SciTech Connect

    Gary Garland

    2015-03-27

    This data set shows the different loading capacities of Media #1 and Media #2 in a high and low salt content brine matrix at different liquid to solid ratio's. These data sets are shaker bath tests on media #1 and media #2 in brine's #1 and #2 at 500mL-.5g(1000-1 ratio), 150mL-.75g(200-1 ratio), and 150mL-2.5g(60-1 ratio) at ambient temperature.

  7. Studies of transport pathways of Th, U, REE's, Ra-228, and Ra-226 from soil to farm animals. Progress report, April 1-December 31, 1983

    SciTech Connect

    Eisenbud, M.; Franca, E.P.

    1984-01-01

    This is a report on the Transport Pathways of Thorium, Uranium, Rare Earths Elements, Radium-228 and Radium-226 from Soil to Farm Animals. The investigation is taking place in the State of Minas Gerais, Brazil, where an ore body (Morro de Ferro) exists that contains about 30,000 metric tons of thorium and more than 50,000 metric tons of rare earth elements. The ore body, which is believed to be about 60 million years old, has eroded to the surface and has been inundated by ground water. Nearby farmers are cooperating in the study. The analytical procedures have been modified to adapt them to the large volumes of biological material. The soils from the farm plots have been sampled, analyzed and characterized by standard pedological methods. Analyses for most of the substances of interest have been completed in pilot samples of vegetables and cow bone.

  8. Physical characterization, magnetic measurements, REE geochemistry and biomonitoring of dust load accumulated during a protracted winter fog period and their implications.

    PubMed

    Chakarvorty, Munmun; Pati, Jayanta Kumar; Patil, Shiva Kumar; Shukla, Swati; Niyogi, Ambalika; Saraf, Arun Kumar

    2014-05-01

    The winter fog in India is a recurrent phenomenon for more than a decade now affecting the entire Himalayan and sub-Himalayan regions covering an area of nearly 500,000 km(2). Every winter (December-January), the air and surface transports in cities of northern India (Amritsar, New Delhi, Agra, Gwalior, Kanpur, Lucknow, and Allahabad) are severely disrupted with visibility reduced to <50 m at times. Since dust particles are known to act as nuclei for the fog formation, this study is aimed to carry out physicochemical characterization of the dust particulates accumulated during a protracted fog period from one of the severely fog affected cities of north India (Allahabad; 25°27'33.40″N-81°52'45.47″E). The dust-loaded tree leaves belonging to Ficus bengalensis and Ficus religiosa from 50 different locations between January 24 and 31, 2010 are sampled and characterized. The mass of dust, color, grain shape, size, phase constituents, and mineral magnetic parameters, such as magnetic susceptibility, SIRM, χ fd%, and S-ratio, show minor variation and the regional influence outweighs local anthropogenic contributions. The dust compositions show fractionated rare earth element pattern with a pronounced negative Eu anomaly similar to upper continental crust and further suggesting their derivation from sources located in parts of north and central India. PMID:24407961

  9. The reliability of ∼2.9 Ga old Witwatersrand banded iron formations (South Africa) as archives for Mesoarchean seawater: Evidence from REE and Nd isotope systematics

    NASA Astrophysics Data System (ADS)

    Viehmann, Sebastian; Bau, Michael; Smith, Albertus J. B.; Beukes, Nicolas J.; Dantas, Elton L.; Bühn, Bernhard

    2015-11-01

    Pure marine chemical sediments, such as (Banded) Iron Formations, (B)IFs, are archives of geochemical proxies for the composition of Precambrian seawater and may provide information about the ancient hydrosphere-atmosphere system. We here present rare earths and yttrium (REY) and high precision Sm-Nd isotope data of ∼2.90 Ga old Superior-type BIFs from the Witwatersrand Supergroup, South Africa, and compare those with data for near-contemporaneous BIFs from the correlative Pongola Supergroup (Superior-type BIF) and from the Pietersburg Greenstone Belt (Algoma-type IF), respectively. All Witwatersrand samples studied display the typical general REY distribution of Archean seawater, but their REY anomalies are less pronounced and their immobile element concentrations are higher than those of other pure (B)IFs. These observations indicate the presence of significant amounts of detrital aluminosilicates in the Witwatersrand BIFs and question the reliability of the Contorted Bed and Water Tower BIFs (Parktown Formation, West Rand Group) as archives of Mesoarchean seawater. Significant post-depositional alteration of the REY budget and the Sm-Nd isotope system is not observed. The Nd isotopic compositions of the purest BIF samples, i.e. the most reliable archives for Witwatersrand seawater, show initial εNd values between -3.95 and -2.25. This range is more negative than what is observed in ambient shales, indicating a decoupling of suspended and dissolved loads in the "near-shore" Witwatersrand Basin seawater. However, εNd range overlaps with that of the correlative Pongola BIF (Alexander et al., 2008). The deeper-water Algoma-type Pietersburg BIF shows more positive (i.e. more mantle-like) εNd2.9Ga values, supporting the hypothesis that a significant amount of its REY inventory was derived from black smoker-style, high-temperature hydrothermal fluids that had altered seafloor basalts. In marked contrast, the dissolved REY budgets (including the Nd isotopic compositions) of the Witwatersrand and Pongola seawater, however, were dominated by similar terrigenous REY sources from the Kaapvaal Craton.

  10. Nb/Ta, Zr/Hf and REE in the depleted mantle: implications for the differentiation history of the crust-mantle system

    NASA Astrophysics Data System (ADS)

    Weyer, Stefan; Münker, Carsten; Mezger, Klaus

    2003-01-01

    High-precision Nb, Ta, Zr, Hf, Sm, Nd and Lu concentration data of depleted mantle rocks from the Balmuccia peridotite complex (Ivrea Zone, Italian Alps) were determined by isotope dilution using multiple collector inductively coupled plasma mass spectrometry (MC-ICPMS) and thermal ionisation mass spectrometry (TIMS). The Zr/Hf ratios of all investigated samples from the Balmuccia peridotite complex are significantly lower than the chondritic value of 34.2, and the most depleted samples have Zr/Hf ratios as low as 10. Correlated Zr/Hf ratios and Zr abundances of the lherzolites preserve the trend of a mantle residue that has been depleted by fractional melting. This trend confirms experimental studies that predict Hf to behave more compatibly than Zr during mantle melting. Experimentally determined partition coefficients imply that the major Zr and Hf depletion most likely occurred in the spinel stability field, with ( DZr/ DHf) cpx≈0.5, and not in the garnet stability field, where ( DZr/ DHf) grt is probably close to one. However, minor amounts of melting must have also occurred in a garnet facies mantle, as indicated by low Sm/Lu ratios in the Balmuccia peridotites. The Nb/Ta ratios of most lherzolites are subchondritic and vary only from 7 to 10, with the exception of three samples that have higher Nb/Ta ratios (18-24). The overall low Nb/Ta ratios of most depleted mantle rocks confirm a higher compatibility of Ta in the mantle. The uniform Nb/Ta ratios in most samples imply that even in 'depleted' mantle domains the budget of the highly incompatible Nb and Ta is controlled by enrichment processes. Such a model is supported by the positive correlation of Zr/Nb with the Zr concentration. However, the overall enrichment was weak and did barely affect the moderately incompatible elements Zr and Hf. The new constraints from the partitioning behaviour of Zr-Hf and Nb-Ta provide important insights into processes that formed the Earth's major silicate reservoirs. The correlation of Zr/Hf and Sm/Nd in depleted MORB can be assigned to previous melting events in the MORB source. However, such trends were unlikely produced during continental crust formation processes, where Sm/Nd and Zr/Hf are decoupled. The different fractionation behaviour of Zr/Hf and Sm/Nd in the depleted mantle (correlated) and the crust (decoupled) indicates that crustal growth by a simple partial melting process in the mantle has little effect on the mass budget of LREE and HFSE between crust and mantle. A more complex source composition, similar to that of modern subduction rocks, is needed to fractionate the LREE, but not Zr/Hf and the HREE.

  11. The Riviera Deposit: Endo-skarn and Vein-hosted W-MO-REE Mineralization in I-type Granites of the Cape Granite Suite, South Africa

    NASA Astrophysics Data System (ADS)

    Rozendaal, A.; Moyen, J.

    2009-05-01

    The blind Riviera deposit is located in the western Cape Province and was discovered by stream sediment sampling in the mid 1970's. Resources total 46 million metric tons assaying 0,216 per cent tungsten and 200 parts per million molybdenum, a marginal grade that has prohibited development into an open cast mine. Mineralization is mainly hosted by granitoids of the Riviera Pluton which intruded the regionally metamorphosed volcano-sedimentary Malmesbury Group. These granitoids form part of the Cape Granite Suite, a series of batholiths and plutons with S-, I- and A-type characteristics. The composite Riviera Pluton comprises a suite of metaluminous to slightly peraluminous granitoids. The rocks least affected by hydrothermal alteration are granodioritic to adamelitic in composition whereas the more altered host rocks include quartz-monzonite, granite and quartz syenite. As a whole the suite is subalkaline to K-calcalkaline and conforms to the characteristics of I-type granites. The pluton was emplaced into a dome-shaped interference structure, late in the Neoproterozoic Saldanian orogenic cycle. Alteration, particularly prevalent in the roof or cupola of the pluton, occurs as zones of pervasive sericitization, argillization, silicification and potassic alteration. Their spatial and temporal relationship is complex and indicates several superimposed alteration events. Wall rocks display limited alteration and have acted as an impermeable cap. The cross-cutting granitoid intrusions produced wall rock xenoliths of various dimensions consisting mainly of meta-carbonates displaying various stages of digestion. Economic concentrations of scheelite are spatially linked to these assimilations, particularly proximal to the wall rock contact. The occurrence of diagnostic minerals such as vesuvianite, hornblende, hedenbergite, grandite garnets define a typical endo-skarn association. Accessory minerals include pyrite, pyrrhotite, chalcopyrite, sphalerite and the LREE enriched mineral allanite. Scheelite and molybdenite occurs as fine disseminations, but also as coarse grains within cross-cutting, late stage quartz and calcite veins in the granite and the wall rocks. No spatial or paragenetic correlation exists between the concentration of tungsten and molybdenum, suggesting that their distribution is related to sequential introduction of multiple magmatic phases and associated mineralizing fluids.

  12. Zr-Y-Nb-REE mineralization associated with microgranite and basic dykes at EL Sela shear zone, South Eastern Desert, Egypt.

    PubMed

    Shahin, Hassan Abd El-Razek Aly

    2014-01-01

    El Sela shear zone occurs in the younger granite rock of Gabal El Sela area, south Eastern Desert, Egypt near the Sudan Frontier. It comprises lines-arranged intrusions trending ENE-WSW and extend for about 1.5 km in length and reach up to 40 meters in width. These lines-arranged intrusions include multi-phase quartz veins, altered microgranite and altered basic dykes. These dykes hosting or acting as a source for uranium, rare metals (Zr, Y, Nb and Ga) and light rare earths (La, Ce, Sm and Nd) mineralizations. They show highly alteration, uranium enrichment and a strong enrichment in some rare metals and light rare earths contents (Zr = 644, Y = 133, Nb = 136, Ga =184, La = 50.19, Ce = 105.47, Sm = 24.81, Nd = 78.91 ppm and and ∑ LREEs = 259.38.). The chondrite normalised rare earth elements trends indicate strongly fractionated rare earth elements pattern with significant enriched of LREE according to HREE in both altered microgranite and altered basic dykes. Field radiometric measurements of the studied altered microgranite dyke revealed that eU reach up to 359 ppm with an average 78 ppm, while in the altered basic dyke reach up to 1625 ppm with an average 144 ppm. PMID:25332873

  13. The role of chloride-carbonate melts in the formation of sideritic carbonatites of the KARASUg FE-F-REE deposit (Tyva Republic, Russia)

    NASA Astrophysics Data System (ADS)

    Prokop'ev, I. R.; Borovikov, A. A.; Pavlova, G. G.; Borisenko, A. S.

    2014-04-01

    The authors have studied melt-fluid and fluid inclusions in quartz and fluorite of sideritic and ankerite-calcitic carbonatites of the Karasug ore field, as well as melt inclusions in apatite from granosyenites. The content of salt and fluid components in brine-melt inclusions was evaluated on the basis of the thermodynamic data, the calculations of volumes and densities of the solid phases, a solution of about 50% concentration, and the gas phase of the inclusions, as well as the results of the LA-ICP-MS analysis. The content of salt phases, the solution, and the gas phase amounted to 85-70, 10-25, and about 5% of the inclusion substance, respectively. The total percentage of salt and fluid components (H2O and CO2) amounted to 90-80 and 10-20 wt %, respectively. The fraction of a carbonate constituent in the inclusions was as high as 45-50% and over in ankerite-calcite carbonatites and about 15 wt % in sideritic carbonatites. The 117.2 ± 1.3 Ma age of these carbonatites by 40Ar/39Ar, along with other datings for this area, shows that their formation was associated with a manifestation of the Cretaceous alkaline-mafic magmatism (117-120 Ma). The presented model of the formation of carbonatites is in agreement with the sequence of the development of magmatic processes and mineralization in this area. The model is also confirmed by the results of the studies of melt and fluid inclusions in minerals.

  14. Rb-Sr and Sm-Nd isotopic and REE studies of igneous components in the bulk matrix domain of Martian breccia Northwest Africa 7034

    NASA Astrophysics Data System (ADS)

    Nyquist, Laurence E.; Shih, Chi-Yu; McCubbin, Francis M.; Santos, Alison R.; Shearer, Charles K.; Peng, Zhan X.; Burger, Paul V.; Agee, Carl B.

    2016-03-01

    The bulk matrix domain of the Martian breccia NWA 7034 was examined petrographically and isotopically to better understand the provenance and age of the source material that make up the breccia. Both 147Sm-143Nd and 146Sm-142Nd age results for mineral separates from the bulk matrix portion of breccia NWA 7034 suggest that various lithological components in the breccia probably formed contemporaneously ~4.44 Ga ago. This old age is in excellent agreement with the upper intersection ages (4.35-4.45 Ga) for U-Pb discordia and also concordia defined by zircon and baddeleyite grains in matrix and igneous-textured clasts. Consequently, we confirm an ancient age for the igneous components that make up the NWA 7034 breccia. Substantial disturbance in the Rb-Sr system was detected, and no age significance could be gleaned from our Rb-Sr data. The disturbance to the Rb-Sr system may be due to a thermal event recorded by bulk-rock K-Ar ages of 1.56 Ga and U-Pb ages of phosphates at about 1.35-1.5 Ga, which suggest partial resetting from an unknown thermal event(s), possibly accompanying breccia formation. The NWA 7034 bulk rock is LREE enriched and similar to KREEP-rich lunar rocks, which indicates that the earliest Martian crust was geochemically enriched. This enrichment supports the idea that the crust is one of the enriched geochemical reservoirs on Mars that have been detected in studies of other Martian meteorites.

  15. A Nd isotopic study of the Hamersley and Michipicoten banded iron formations - The source of REE and Fe in Archean oceans

    NASA Technical Reports Server (NTRS)

    Jacobsen, Stein B.; Pimentel-Klose, Mario R.

    1988-01-01

    A detailed Nd isotopic study of the large and well-dated Hamersley and Michipicoten banded iron formations (BIFs) has been conducted. The Hamersley BIFs (Lake Superior type) are located in the Pilbara craton of Western Australia and the Michipicoten BIFs (Algoma type) are located in the northeastern corner of Lake Superior in Ontario, Canada. Their initial epsilon(Nd) values are variable and in the range of 0 to +4. The Fe/Nd ratio in present-day hydrothermal waters and BIFs are both 100,000, suggesting that the source of much of the Fe in BIFs (and Archean seawater) was hydrothermal water circulating through Archean midocean ridge systems.

  16. Rapid Research Methods for Nurses, Midwives and Health Professionals Rees Colin Rapid Research Methods for Nurses, Midwives and Health Professionals 144pp £19.99 Wiley Blackwell 9781119048411 1119048419 [Formula: see text].

    PubMed

    2016-07-20

    Being able to understand research language is a requisite for the contemporary nurse in the era of evidence-based care provision. The user-friendly text provides extremely accessible information for this purpose. PMID:27440355

  17. Using wavelet analysis to compare the QCD prediction and experimental data on R_{e^+e^-} and to determine parameters of the charmonium states above the Dbar{D} threshold

    NASA Astrophysics Data System (ADS)

    Henner, V. K.; Davis, C. L.; Belozerova, T. S.

    2015-10-01

    The first part of our analysis uses the wavelet method to compare the quantum chromodynamic (QCD) prediction for the ratio of hadronic to muon cross sections in electron-positron collisions, R, with experimental data for R over a center of mass energy range up to about 7 GeV. A direct comparison of the raw experimental data and the QCD prediction is difficult because the data have a wide range of structures and large statistical errors and the QCD description contains sharp quark-antiquark thresholds. However, a meaningful comparison can be made if a type of "smearing" procedure is used to smooth out rapid variations in both the theoretical and experimental values of R. A wavelet analysis (WA) can be used to achieve this smearing effect. The second part of the analysis concentrates on the 3.0-6.0 GeV energy region which includes the relatively wide charmonium resonances ψ (1^-). We use the wavelet methodology to distinguish these resonances from experimental noise, background and from each other, allowing a reliable determination of the parameters of these states. Both analyses are examples of the usefulness of WA in extracting information in a model independent way from high energy physics data.

  18. Sm Nd isotope systematics and REE data for leucotroctolites and their amphibolitized equivalents of the Niquelândia Complex upper layered series, central Brazil: further constraints for the timing of magmatism and high-grade metamorphism

    NASA Astrophysics Data System (ADS)

    Ferreira Filho, C. F.; Pimentel, M. M.

    2000-12-01

    The Barro Alto, Niquelândia, and Cana Brava Complexes are major Proterozoic layered intrusions in central Brazil that were affected by high-grade metamorphism with associated ductile deformation during the Neoproterozoic (770-795 Ma). Recent studies recognized that the Niquelândia Complex comprises two petrologically distinct and tectonically juxtaposed magmatic systems: a younger Upper Layered Series to the west and an older Lower Layered Series to the east. Previous geochronological studies on Lower Series rocks suggested a Paleoproterozoic (ca 2.0 Ga) age for the Lower Series magmatic event. New trace element data matched with Sm-Nd isotope data for Upper Series samples yielded well-constrained and original geochronological information. The 1.35 Ga age of the Upper Series magmatism reported in this paper indicates a much younger age of the Upper Series compared with the Lower Series. The tectonic contact between these two distinct magmatic systems is now raised to the category of a major Paleo-Mesoproterozoic crustal discontinuity.

  19. Geochemistry of some rare earth elements in groundwater, Vierlingsbeek, The Netherlands.

    PubMed

    Janssen, René P T; Verweij, Wilko

    2003-03-01

    Groundwater samples were taken from seven bore holes at depths ranging from 2 to 41m nearby drinking water pumping station Vierlingsbeek, The Netherlands and analysed for Y, La, Ce, Pr, Nd, Sm and Eu. Shale-normalized patterns were generally flat and showed that the observed rare earth elements (REE) were probably of natural origin. In the shallow groundwaters the REEs were light REE (LREE) enriched, probably caused by binding of LREEs to colloids. To improve understanding of the behaviour of the REE, two approaches were used: calculations of the speciation and a statistical approach. For the speciation calculations, complexation and precipitation reactions including inorganic and dissolved organic carbon (DOC) compounds, were taken into account. The REE speciation showed REE(3+), REE(SO(4))(+), REE(CO(3))(+) and REE(DOC) being the major species. Dissolution of pure REE precipitates and REE-enriched solid phases did not account for the observed REEs in groundwater. Regulation of REE concentrations by adsorption-desorption processes to Fe(III)(OH)(3) and Al(OH)(3) minerals, which were calculated to be present in nearly all groundwaters, is a probable explanation. The statistical approach (multiple linear regression) showed that pH is by far the most significant groundwater characteristic which contributes to the variation in REE concentrations. Also DOC, SO(4), Fe and Al contributed significantly, although to a much lesser extent, to the variation in REE concentrations. This is in line with the calculated REE-species in solution and REE-adsorption to iron and aluminium (hydr)oxides. Regression equations including only pH, were derived to predict REE concentrations in groundwater. External validation showed that these regression equations were reasonably successful to predict REE concentrations of groundwater of another drinking water pumping station in quite different region of The Netherlands. PMID:12598196

  20. Factors affecting the rare earth element compositions in massive sulfides from deep-sea hydrothermal systems

    NASA Astrophysics Data System (ADS)

    Zeng, Zhigang; Ma, Yao; Yin, Xuebo; Selby, David; Kong, Fancui; Chen, Shuai

    2015-09-01

    To reconstruct the evolution of ore-forming fluids and determine the physicochemical conditions of deposition associated with seafloor massive sulfides, we must better understand the sources of rare earth elements (REEs), the factors that affect the REE abundance in the sulfides, and the REE flux from hydrothermal fluids to the sulfides. Here we examine the REE profiles of 46 massive sulfide samples collected from seven seafloor hydrothermal systems. These profiles feature variable total REE concentrations (37.2-4092 ppb) and REE distribution patterns (LaCN/LuCN ratios = 2.00-73.8; (Eu/Eu*)CN ratios = 0.34-7.60). The majority of the REE distribution patterns in the sulfides are similar to those of vent fluids, with the sulfides also exhibiting light REE enrichment. We demonstrate that the variable REE concentrations, Eu anomalies, and fractionation between light REEs and heavy REEs in the sulfides exhibit a relationship with the REE properties of the sulfide-forming fluids and the massive sulfide chemistry. Based on the sulfide REE data, we estimate that modern seafloor sulfide deposits contain approximately 280 t of REEs. According to the flux of hydrothermal fluids at mid-ocean ridges (MORs) and an average REE concentration of 3 ng/g in these fluids, hydrothermal vents at MORs alone transport more REEs (>360 t) to the oceans over the course of just 2 years than the total quantity of REEs in seafloor sulfides. The excess REEs (i.e., the quantity not captured by massive sulfides) may be transported away from the systems and become bound in sulfate deposits and metalliferous sediments.

  1. Health effects and toxicity mechanisms of rare earth elements-Knowledge gaps and research prospects.

    PubMed

    Pagano, Giovanni; Guida, Marco; Tommasi, Franca; Oral, Rahime

    2015-05-01

    In the recent decades, rare earth elements (REE) have undergone a steady spread in several industrial and medical applications, and in agriculture. Relatively scarce information has been acquired to date on REE-associated biological effects, from studies of bioaccumulation and of bioassays on animal, plant and models; a few case reports have focused on human health effects following occupational REE exposures, in the present lack of epidemiological studies of occupationally exposed groups. The literature is mostly confined to reports on few REE, namely cerium and lanthanum, whereas substantial information gaps persist on the health effects of other REE. An established action mechanism in REE-associated health effects relates to modulating oxidative stress, analogous to the recognized redox mechanisms observed for other transition elements. Adverse outcomes of REE exposures include a number of endpoints, such as growth inhibition, cytogenetic effects, and organ-specific toxicity. An apparent controversy regarding REE-associated health effects relates to opposed data pointing to either favorable or adverse effects of REE exposures. Several studies have demonstrated that REE, like a number of other xenobiotics, follow hormetic concentration-related trends, implying stimulatory or protective effects at low levels, then adverse effects at higher concentrations. Another major role for REE-associated effects should be focused on pH-dependent REE speciation and hence toxicity. Few reports have demonstrated that environmental acidification enhances REE toxicity; these data may assume particular relevance in REE-polluted acidic soils and in REE mining areas characterized by concomitant REE and acid pollution. The likely environmental threats arising from REE exposures deserve a new line of research efforts. PMID:25679485

  2. Recovery and Separation of Rare Earth Elements Using Salmon Milt

    PubMed Central

    Takahashi, Yoshio; Kondo, Kazuhiro; Miyaji, Asami; Watanabe, Yusuke; Fan, Qiaohui; Honma, Tetsuo; Tanaka, Kazuya

    2014-01-01

    Recycling rare earth elements (REEs) used in advanced materials such as Nd magnets is important for the efficient use of REE resources when the supply of several REEs is limited. In this work, the feasibility of using salmon milt for REE recovery and separation was examined, along with the identification of the binding site of REEs in salmon milt. Results showed that (i) salmon milt has a sufficiently high affinity to adsorb REEs and (ii) the adsorption capacity of the milt is 1.04 mEq/g, which is comparable with that of commercial cation exchange resin. Heavier REEs have higher affinity for milt. A comparison of stability constants and adsorption patterns of REEs discussed in the literature suggests that the phosphate is responsible for the adsorption of REE in milt. The results were supported by dysprosium (Dy) and lutetium (Lu) LIII-edge extended x-ray absorption fine structure (EXAFS) spectroscopy. The REE-P shell was identified for the second neighboring atom, which shows the importance of the phosphate site as REE binding sites. The comparison of REE adsorption pattern and EXAFS results between the milt system and other adsorbent systems (cellulose phosphate, Ln-resin, bacteria, and DNA-filter hybrid) revealed that the coordination number of phosphate is correlated with the slope of the REE pattern. The separation column loaded with milt was tested to separate REE for the practical use of salmon milt for the recovery and separation of REE. However, water did not flow through the column possibly because of the hydrophobicity of the milt. Thus, sequential adsorption–desorption approach using a batch-type method was applied for the separation of REE. As an example of the practical applications of REE separation, Nd and Fe(III) were successfully separated from a synthetic solution of Nd magnet waste by a batch-type method using salmon milt. PMID:25490035

  3. Uptake of Germanium and Rare Earth Elements (La, Gd, Er, Nd) by white mustard (Brassica alba L.) and common millet (Panicum milliaceum L.) as affected by Phosphorus Nutrition

    NASA Astrophysics Data System (ADS)

    Zill, Juliane; Wiche, Oliver

    2015-04-01

    The effect of phosphate nutrition is important due to the future usage of fertilizer treatment in phytomining experiments e.g. in accumulation of the economically important rare earth elements (REE). It is expected that the trivalent charge of REE will result in complexation with phosphate and REEs could be immobilized and not further bioavailable for plants which would cause losses of REE concentration in biomass. To investigate this influence on lanthanum, neodymium, gadolinium and erbium two plant species Brassica alba (white mustard) and Panicum miliaceum (common millet) were cultured in a greenhouse study. The plants were cultivated onto two different substrates and were poured with modified REE and phosphate solutions within an eight-week period. The concentrations of REE in soil, soil solution and plant samples were determined by inductively coupled plasma-mass spectrometry (ICP-MS). The results show an increase of concentration of REE with increasing levels of element solution applied for both species. REE accumulations are elevated in roots and decrease in the order of roots> leaves> stem> fruit/blossom. Brassica accumulated more REE in root whereas Panicum showed higher REE concentrations in leaves. Exposure to increased phosphate addition did not significantly change the concentrations of REE in both plant species yet the REE concentrations in leaves slightly decreased with increasing phosphate addition. For root and stem no precise trend could be determined. It is most likely that REEs precipitate with phosphate on root surfaces and in the roots. The bioavailability of REE to plants is affected by complexation processes of REEs with phosphate in the rhizosphere. The results indicate that phosphate application plays an important role on REE uptake by roots and accumulation in different parts of a plant and it might have an influence on translocation of REE within the plant.

  4. Bacterial Cell Surface Adsorption of Rare Earth Elements

    NASA Astrophysics Data System (ADS)

    Jiao, Y.; Park, D.; Reed, D.; Fujita, Y.; Yung, M.; Anderko, A.; Eslamimanesh, A.

    2015-12-01

    Rare earth elements (REE) play a critical role in many emerging clean energy technologies, including high-power magnets, wind turbines, solar panels, hybrid/electric vehicle batteries and lamp phosphors. In order to sustain demand for such technologies given current domestic REE shortages, there is a need to develop new approaches for ore processing/refining and recycling of REE-containing materials. To this end, we have developed a microbially-mediated bioadsorption strategy with application towards enrichment of REE from complex mixtures. Specifically, the bacterium Caulobacter crescentus was genetically engineered to display lanthanide binding tags (LBTs), short peptides that possess high affinity and specificity for rare earth elements, on its cell surface S-layer protein. Under optimal conditions, LBT-displayed cells adsorbed greater than 5-fold more REE than control cells lacking LBTs. Competition binding experiments with a selection of REEs demonstrated that our engineered cells could facilitate separation of light- from heavy- REE. Importantly, binding of REE onto our engineered strains was much more favorable compared to non-REE metals. Finally, REE bound to the cell surface could be stripped off using citrate, providing an effective and non-toxic REE recovery method. Together, this data highlights the potential of our approach for selective REE enrichment from REE containing mixtures.

  5. The rare-earth elements: vital to modern technologies and lifestyles

    USGS Publications Warehouse

    Van Gosen, Bradley S.; Verplanck, Philip L.; Long, Keith R.; Gambogi, Joseph; Seal, Robert R., II

    2014-01-01

    Since the late 1990s, China has provided 85–95 percent of the world’s REEs. In 2010, China announced their intention to reduce REE exports. During this timeframe, REE use increased substantially. REEs are used as components in high technology devices, including smart phones, digital cameras, computer hard disks, fluorescent and light-emitting-diode (LED) lights, flat screen televisions, computer monitors, and electronic displays. Large quantities of some REEs are used in clean energy and defense technologies. Because of the many important uses of REEs, nations dependent on new technologies, such as Japan, the United States, and members of the European Union, reacted with great concern to China’s intent to reduce its REE exports. Consequently, exploration activities intent on discovering economic deposits of REEs and bringing them into production have increased.

  6. Dr. Wernher Von Braun

    NASA Technical Reports Server (NTRS)

    1999-01-01

    Dr. Wernher von Braun with Dr. Eberhard Rees and R.W. Cook at a press conference concerning Dr. Von Braun's assignment to NASA headquarters and Dr. Rees' subsequent assignment as Marshall Center director.

  7. Geology and market-dependent significance of rare earth element resources

    NASA Astrophysics Data System (ADS)

    Simandl, G. J.

    2014-09-01

    China started to produce rare earth elements (REEs) in the 1980s, and since the mid-1990s, it has become the dominant producer. Rare earth element export quotas first introduced by the Chinese government in the early 2000s were severely reduced in 2010 and 2011. This led to strong government-created disparity between prices within China and the rest of the world. Industrialized countries identified several REEs as strategic metals. Because of rapid price increases of REE outside of China, we have witnessed a world-scale REE exploration rush. The REE resources are concentrated in carbonatite-related deposits, peralkaline igneous rocks, pegmatites, monazite ± apatite veins, ion adsorption clays, placers, and some deep ocean sediments. REE could also be derived as a by-product of phosphate fertilizer production, U processing, mining of Ti-Zr-bearing placers, and exploitation of Olympic Dam subtype iron oxide copper gold (IOCG) deposits. Currently, REEs are produced mostly from carbonatite-related deposits, but ion adsorption clay deposits are an important source of heavy REE (HREE). Small quantities of REE are derived from placer deposits and one peralkaline intrusion-related deposit. The ideal REE development targets would be located in a politically stable jurisdiction with a pro-mining disposition such as Canada and Australia. REE grade, HREE/light REE (LREE) ratio of the mineralization, tonnage, mineralogy, and permissive metallurgy are some of the key technical factors that could be used to screen potential development projects. As REEs are considered strategic metals from economic, national security, and environmental points of view, technical and economic parameters alone are unlikely to be used in REE project development decision-making. Recycling of REE is in its infancy and unless legislated, in the short term, it is not expected to contribute significantly to the supply of REE.

  8. Repetitive Regeneration of Media #1 in a Dynamic Column Extraction using Brine #1

    SciTech Connect

    Gary Garland

    2015-10-14

    This data is from a regeneration study from a dynamic column extraction experiment where we ran a solution of REE's through a column of media #1 then stripped the REE's off the media using 2M HNO3 solution. We then re-equilibrated the media and repeated the process of running a REE solution through the column and stripping the REE's off the media and comparing the two runs.

  9. Geology and market-dependent significance of rare earth element resources

    NASA Astrophysics Data System (ADS)

    Simandl, G. J.

    2014-12-01

    China started to produce rare earth elements (REEs) in the 1980s, and since the mid-1990s, it has become the dominant producer. Rare earth element export quotas first introduced by the Chinese government in the early 2000s were severely reduced in 2010 and 2011. This led to strong government-created disparity between prices within China and the rest of the world. Industrialized countries identified several REEs as strategic metals. Because of rapid price increases of REE outside of China, we have witnessed a world-scale REE exploration rush. The REE resources are concentrated in carbonatite-related deposits, peralkaline igneous rocks, pegmatites, monazite ± apatite veins, ion adsorption clays, placers, and some deep ocean sediments. REE could also be derived as a by-product of phosphate fertilizer production, U processing, mining of Ti-Zr-bearing placers, and exploitation of Olympic Dam subtype iron oxide copper gold (IOCG) deposits. Currently, REEs are produced mostly from carbonatite-related deposits, but ion adsorption clay deposits are an important source of heavy REE (HREE). Small quantities of REE are derived from placer deposits and one peralkaline intrusion-related deposit. The ideal REE development targets would be located in a politically stable jurisdiction with a pro-mining disposition such as Canada and Australia. REE grade, HREE/light REE (LREE) ratio of the mineralization, tonnage, mineralogy, and permissive metallurgy are some of the key technical factors that could be used to screen potential development projects. As REEs are considered strategic metals from economic, national security, and environmental points of view, technical and economic parameters alone are unlikely to be used in REE project development decision-making. Recycling of REE is in its infancy and unless legislated, in the short term, it is not expected to contribute significantly to the supply of REE.

  10. Human and Financial Capital in the Rural Educational Environment: The Effects of Exceeding the Carrying Capacity Threshold on Standardized Test Scores in Rural Indiana.

    ERIC Educational Resources Information Center

    Peoples, Glenn

    The Rural Educational Environment (REE) is a complex mixture of demographic and economic forces that interact to impact the rural school corporation. The condition of REE financial and human capital indicates REE health and may influence student performance on standardized tests. This paper proposes an ecosystem model of the impact of financial,…

  11. Selective Extraction of Rare Earth Elements from Permanent Magnet Scraps with Membrane Solvent Extraction

    SciTech Connect

    Kim, Daejin; Powell, Lawrence E.; Delmau, Lætitia H.; Peterson, Eric S.; Herchenroeder, Jim; Bhave, Ramesh R.

    2015-06-24

    In this paper, the rare earth elements (REEs) such as neodymium, praseodymium, and dysprosium were successfully recovered from commercial NdFeB magnets and industrial scrap magnets via membrane assisted solvent extraction (MSX). A hollow fiber membrane system was evaluated to extract REEs in a single step with the feed and strip solutions circulating continuously through the MSX system. The effects of several experimental variables on REE extraction such as flow rate, concentration of REEs in the feed solution, membrane configuration, and composition of acids were investigated with the MSX system. A multimembrane module configuration with REEs dissolved in aqueous nitric acid solutions showed high selectivity for REE extraction with no coextraction of non-REEs, whereas the use of aqueous hydrochloric acid solution resulted in coextraction of non-REEs due to the formation of chloroanions of non-REEs. The REE oxides were recovered from the strip solution through precipitation, drying, and annealing steps. Finally, the resulting REE oxides were characterized with XRD, SEM-EDX, and ICP-OES, demonstrating that the membrane assisted solvent extraction is capable of selectively recovering pure REEs from the industrial scrap magnets.

  12. Selective Extraction of Rare Earth Elements from Permanent Magnet Scraps with Membrane Solvent Extraction

    DOE PAGESBeta

    Kim, Daejin; Powell, Lawrence E.; Delmau, Lætitia H.; Peterson, Eric S.; Herchenroeder, Jim; Bhave, Ramesh R.

    2015-06-24

    In this paper, the rare earth elements (REEs) such as neodymium, praseodymium, and dysprosium were successfully recovered from commercial NdFeB magnets and industrial scrap magnets via membrane assisted solvent extraction (MSX). A hollow fiber membrane system was evaluated to extract REEs in a single step with the feed and strip solutions circulating continuously through the MSX system. The effects of several experimental variables on REE extraction such as flow rate, concentration of REEs in the feed solution, membrane configuration, and composition of acids were investigated with the MSX system. A multimembrane module configuration with REEs dissolved in aqueous nitric acidmore » solutions showed high selectivity for REE extraction with no coextraction of non-REEs, whereas the use of aqueous hydrochloric acid solution resulted in coextraction of non-REEs due to the formation of chloroanions of non-REEs. The REE oxides were recovered from the strip solution through precipitation, drying, and annealing steps. Finally, the resulting REE oxides were characterized with XRD, SEM-EDX, and ICP-OES, demonstrating that the membrane assisted solvent extraction is capable of selectively recovering pure REEs from the industrial scrap magnets.« less

  13. Growth Failure in Children with Intractable Epilepsy Is Not Due to Increased Resting Energy Expenditure

    ERIC Educational Resources Information Center

    Bergqvist, A. G. Christina; Trabulsi, Jillian; Schall, Joan I.; Stallings, Virginia A.

    2008-01-01

    The aim of this study was to evaluate the resting energy expenditure (REE) of children with intractable epilepsy (IE) compared with healthy children, and to determine factors that contribute to the pattern of REE. REE, growth status, and body composition were assessed in 25 prepubertal children with IE (15 males, 10 females; mean age 5y 5mo [SD 2y…

  14. Global demand for rare earth resources and strategies for green mining

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Rare earths elements (REEs) are essential raw materials for the emerging green (low-carbon) energy technologies and ‘smart’ electronic devices. Global REE demand is slated to grow at a compound annual rate of 5% by 2020. Such high growth rate would require a steady supply base of REEs in the long ru...

  15. Selective Extraction of Rare Earth Elements from Permanent Magnet Scraps with Membrane Solvent Extraction.

    PubMed

    Kim, Daejin; Powell, Lawrence E; Delmau, Lætitia H; Peterson, Eric S; Herchenroeder, Jim; Bhave, Ramesh R

    2015-08-18

    The rare earth elements (REEs) such as neodymium, praseodymium, and dysprosium were successfully recovered from commercial NdFeB magnets and industrial scrap magnets via membrane assisted solvent extraction (MSX). A hollow fiber membrane system was evaluated to extract REEs in a single step with the feed and strip solutions circulating continuously through the MSX system. The effects of several experimental variables on REE extraction such as flow rate, concentration of REEs in the feed solution, membrane configuration, and composition of acids were investigated with the MSX system. A multimembrane module configuration with REEs dissolved in aqueous nitric acid solutions showed high selectivity for REE extraction with no coextraction of non-REEs, whereas the use of aqueous hydrochloric acid solution resulted in coextraction of non-REEs due to the formation of chloroanions of non-REEs. The REE oxides were recovered from the strip solution through precipitation, drying, and annealing steps. The resulting REE oxides were characterized with XRD, SEM-EDX, and ICP-OES, demonstrating that the membrane assisted solvent extraction is capable of selectively recovering pure REEs from the industrial scrap magnets. PMID:26107531

  16. Metal loading effect on rare earth element binding to humic acid: Experimental and modelling evidence

    NASA Astrophysics Data System (ADS)

    Marsac, Rémi; Davranche, Mélanie; Gruau, Gérard; Dia, Aline

    2010-03-01

    The effect of metal loading on the binding of rare earth elements (REE) to humic acid (HA) was studied by combining ultrafiltration and Inductively Coupled Plasma Mass Spectrometry techniques. REE-HA complexation experiments were performed at pH 3 for REE/C molar ratios ranging from ca 4 × 10 -4 to 2.7 × 10 -2. Results show that the relative amount of REE bound to HA strongly increases with decreasing REE/C. A middle-REE (MREE) downward concavity is shown by patterns at high metal loading, whereas patterns at low metal loading display a regular increase from La to Lu. Humic Ion Model VI modelling are close to the experimental data variations, provided that (i) the ΔLK 2 parameter (i.e. the Model VI parameter taken into account the presence of strong but low density binding sites) is allowed to increase regularly from La to Lu (from 1.1 to 2.1) and (ii) the published log KMA values (i.e. the REE-HA binding constants specific to Model VI) are slightly modified, in particular with respect to heavy REE. Modelling approach provided evidence that logKdREE patterns with varying REE/C likely arises because REE binding to HA occurs through two types of binding sites in different density: (i) a few strong sites that preferentially complex the heavy REE and thus control the logKdREE atterns at low REE/C; (ii) a larger amount of weaker binding sites that preferentially complex the middle-REE and thus control the logKdREE pattern at high REE/C. Hence, metal loading exerts a major effect on HA-mediated REE binding, which could explain the diversity of published conditional constants for REE binding with HA. A literature survey suggests that the few strong sites activated at low REE/C could be multidentate carboxylic sites, or perhaps N-, or P-functional groups. Finally, an examination of the literature field data proposed that the described loading effect could account for much of the variation in REE patterns observed in natural organic-rich waters (DOC > 5 mg L -1 and 4

  17. Geochemical investigation of Archaean Bimodal and Dwalile metamorphic suites, Ancient Gneiss Complex, Swaziland

    USGS Publications Warehouse

    Hunter, D.R.; Barker, F.; Millard, H.T., Jr.

    1984-01-01

    The bimodal suite (BMS) comprises leucotonalitic and trondhjemitic gneisses interlayered with amphibolites. Based on geochemical parameters three main groups of siliceous gneiss are recognized: (i) SiO2 14%, and fractionated light rare-earth element (REE) and flat heavy REE patterns; (ii) SiO2 and Al2O3 contents similar to (i) but with strongly fractionated REE patterns with steep heavy REE slopes; (iii) SiO2 > 73%, Al2O3 < 14%, Zr ??? 500 ppm and high contents of total REE having fractionated light REE and flat heavy REE patterns with large negative Eu anomalies. The interlayered amphibolites have major element abundances similar to those of basaltic komatiites, Mg-tholeiites and Fe-rich tholeiites. The former have gently sloping REE patterns, whereas the Mg-tholeiites have non-uniform REE patterns ranging from flat (??? 10 times chondrite) to strongly light REE-enriched. The Fe-rich amphibolites have flat REE patterns at 20-30 times chondrite. The Dwalile metamorphic suite, which is preserved in the keels of synforms within the BMS, includes peridotitic komatiites that have depleted light REE patterns similar to those of compositionally similar volcanics in the Onverwacht Group, Barberton, basaltic komatiites and tholeiites. The basaltic komatiites have REE patterns parallel to those of the BMS basaltic komatiites but with lower total REE contents. The Dwalile tholeiites have flat REE patterns. The basic and ultrabasic liquids were derived by partial melting of a mantle source which may have been heterogeneous or the heterogeneity may have resulted from sequential melting of the mantle source. The Fe-rich amphibolites were derived either from liquids generated at shallow levels or from liquids generated at depth which subsequently underwent extensive fractionation. ?? 1984.

  18. Rare earth element patterns in biotite, muscovite and tourmaline minerals

    SciTech Connect

    Laul, J.C.; Lepel, E.A.

    1986-04-21

    Rare earth element concentrations in the minerals biotite and muscovite from the mica schist country rocks of the Etta pegmatite and tourmalines from the Bob Ingersoll pegmatite have been measured by INAA and CNAA. The concentrations range from 10/sup -4/ g/g to 10/sup -10g//sub g/. The REE patterns of biotite, muscovite and tourmaline reported herein are highly fractionated from light to heavy REE. The REE concentrations in biotite and muscovite are high and indigenous. The pegmatite tourmalines contain low concentrations of REE. Variations in tourmaline REE patterns reflect the geochemical evolution of pegmatite melt/fluid system during crystallization.

  19. Hydroxylamine hydrochloride-acetic acid-soluble and -insoluble fractions of pelagic sediment: Readsorption revisited

    USGS Publications Warehouse

    Piper, D.Z.; Wandless, G.A.

    1992-01-01

    The extraction of the rare earth elements (REE) from deep-ocean pelagic sediment, using hydroxylamine hydrochloride-acetic acid, leads to the separation of approximately 70% of the bulk REE content into the soluble fraction and 30% into the insoluble fraction. The REE pattern of the soluble fraction, i.e., the content of REE normalized to average shale on an element-by-element basis and plotted against atomic number, resembles the pattern for seawater, whereas the pattern, as well as the absolute concentrations, in the insoluble fraction resembles the North American shale composite. These results preclude significant readsorption of the REE by the insoluble phases during the leaching procedure.

  20. Extraction of rare earth elements from hydrate-phosphate precipitates of apatite processing

    NASA Astrophysics Data System (ADS)

    Andropov, M. O.; Anufrieva, A. V.; Buynovskiy, A. S.; Makaseev, Y. N.; Mazov, I. N.; Nefedov, R. A.; Sachkov, V. I.; Stepanova, O. B.; Valkov, AV

    2016-01-01

    The features of extraction of rare earth elements (REE) were considered from hydrate-phosphate precipitates of REE of apatite processing by nitric acid technology. The preliminary purification of nitrate solution of REE from impurities of titanium, aluminum, iron, uranium and thorium was suggested to obtain stable solutions not forming precipitates. Washing the extract was recommended with the evaporated reextract that allows to obtain directly on the cascade of REE extraction the concentrated solutions suitable for the separation into groups by the extraction method. Technical decisions were suggested for the separation of REE in groups without the use of salting-out agent.

  1. Rare-Earth Elements in Lighting and Optical Applications and Their Recycling

    NASA Astrophysics Data System (ADS)

    Song, Xin; Chang, Moon-Hwan; Pecht, Michael

    2013-10-01

    Rare-earth elements (REEs) are used in lighting and optical applications to enable color and light adjustment, miniaturization, and energy efficiency. Common applications of REEs include phosphors for light-emitting diodes, lasers, and electronic video displays. This article reviews how REEs are widely used in these applications. However, supply constraints, including rising prices, environmental concerns over mining and refining processes, and China's control over the supply of the vast majority of REEs, are of concern for manufacturers. In view of these supply constraints, this article discusses ways for manufacturers of lighting and optical devices to identify potential substitutes and recycling methods for REEs.

  2. A new predictive equation for resting energy expenditure in healthy individuals.

    PubMed

    Mifflin, M D; St Jeor, S T; Hill, L A; Scott, B J; Daugherty, S A; Koh, Y O

    1990-02-01

    A predictive equation for resting energy expenditure (REE) was derived from data from 498 healthy subjects, including females (n = 247) and males (n = 251), aged 19-78 y (45 +/- 14 y, mean +/- SD). Normal-weight (n = 264) and obese (n = 234) individuals were studied and REE was measured by indirect calorimetry. Multiple-regression analyses were employed to drive relationships between REE and weight, height, and age for both men and women (R2 = 0.71): REE = 9.99 x weight + 6.25 x height - 4.92 x age + 166 x sex (males, 1; females, 0) - 161. Simplification of this formula and separation by sex did not affect its predictive value: REE (males) = 10 x weight (kg) + 6.25 x height (cm) - 5 x age (y) + 5; REE (females) = 10 x weight (kg) + 6.25 x height (cm) - 5 x age (y) - 161. The inclusion of relative body weight and body-weight distribution did not significantly improve the predictive value of these equations. The Harris-Benedict Equations derived in 1919 overestimated measured REE by 5% (p less than 0.01). Fat-free mass (FFM) was the best single predictor of REE (R2 = 0.64): REE = 19.7 x FFM + 413. Weight also was closely correlated with REE (R2 = 0.56): REE = 15.1 x weight + 371. PMID:2305711

  3. Rare earth element distributions and fractionation in plankton from the northwestern Mediterranean Sea.

    PubMed

    Strady, Emilie; Kim, Intae; Radakovitch, Olivier; Kim, Guebuem

    2015-01-01

    Rare earth element (REE) concentrations were measured for the first time in plankton from the northwestern Mediterranean Sea. The REE concentrations in phytoplankton (60-200 μm) were 5-15 times higher than those in four size fractions of zooplankton: 200-500 μm, 500-1000 μm, 1000-2000 μm and >2000 μm. The concentrations within these zooplankton fractions exhibited the same ranges with some variation attributed to differences in zooplankton taxonomy. The REE concentrations in plankton were poorly related to the reported REE concentrations of seawater, but they correlated well with the calculated REE(3+), concentrations especially with regard to middle REE (MREEs) and heavy REEs (HREEs). Plankton and seawater revealed different PAAS-normalised REE distributions, with the greatest differences observed in the light REEs. Interestingly, a comparison of PAAS-normalized sediment particles from the study of Fowler et al. (1992) showed concentrations of the same order of magnitude and a similar REE distribution without MREE enrichment. Based on this comparison, we propose a conceptual model that emphasizes the importance of biological scavenging of REEs (especially LREEs) in surface waters. PMID:24972173

  4. The role of phosphorus in lunar samples - A chemical study

    NASA Technical Reports Server (NTRS)

    Jovanovic, S.; Reed, G. W., Jr.

    1983-01-01

    Phases rapidly dissolved by pH1 HNO3 acid are found in up to 60% of the REE, P, U, and halogens in basalt 75055, basalt mineral separates, KREEP-rich breccia 14312, and components from highland breccia 66095. This suggests that they may be phosphates. The 0.1 M HNO3 soluble fractions from whole rock breccias 14312 and 66095, and 60095 matrix, and a melt rock clast, have similar REE patterns. This implies that the same major REE-bearing phase is common to all the samples. The postleach residues contain REE in other phases. The acid-soluble phases associated with separated minerals from 75055 are depleted in REE relative to P, and also relative to REE and P in the bulk igneous rock. This may be interpreted as partitioning of REE present at grain surfaces into the major minerals.

  5. Geochemistry of rare earth elements in a passive treatment system built for acid mine drainage remediation.

    PubMed

    Prudêncio, Maria Isabel; Valente, Teresa; Marques, Rosa; Sequeira Braga, Maria Amália; Pamplona, Jorge

    2015-11-01

    Rare earth elements (REE) were used to assess attenuation processes in a passive system for acid mine drainage treatment (Jales, Portugal). Hydrochemical parameters and REE contents in water, soils and sediments were obtained along the treatment system, after summer and winter. A decrease of REE contents in the water resulting from the interaction with limestone after summer occurs; in the wetlands REE are significantly released by the soil particles to the water. After winter, a higher water dynamics favors the AMD treatment effectiveness and performance since REE contents decrease along the system; La and Ce are preferentially sequestered by ochre sludge but released to the water in the wetlands, influencing the REE pattern of the creek water. Thus, REE fractionation occurs in the passive treatment systems and can be used as tracer to follow up and understand the geochemical processes that promote the remediation of AMD. PMID:26247412

  6. Rare earth and trace element geochemistry of a fragment of Jurassic seafloor, Point Sal, California

    NASA Technical Reports Server (NTRS)

    Menzies, M.; Blanchard, D.; Brannon, J.; Korotev, R.

    1977-01-01

    Rocks from an ophiolite suite once on the seafloor were analyzed for rare earth elements (REE), Sc, Co, Na2O, Cr, Zn and FeO. Strontium isotope exchange noted in some of the lavas is attributed to basalt-seawater interaction; the Ce abundance in smectite- and zeolite-bearing lavas may also be due to prolonged exposure to seawater. The higher grades of metamorphic rock, however, show no variation from the usual flat or slightly light REE depleted profiles. Plutonic igneous rock, all light REE depleted, have total REE abundances varying by a factor of 100 between the dunites and diorites. In order of decreasing REE abundance are hornblende, clinopyroxene, plagioclase, orthopyroxene and olivine. Calculations of REE contents of liquids in equilibrium with early cumulative clinopyroxenes suggest that the parent to the stratiform sequence was more depleted in light REE than the parent to the lava pile.

  7. Geochemistry of rare earth elements in Permian coals from the Huaibei Coalfield, China

    USGS Publications Warehouse

    Zheng, Lingyun; Liu, Gaisheng; Chou, C.-L.; Qi, C.; Zhang, Y.

    2007-01-01

    The rare earth elements (REEs) in coals are important because of: (a) REE patterns can be an indicator of the nature of source rocks of the mineral matter as well as sedimentary environments; (b) REEs abundance in coal may have industrial-significance. In this study, a total of thirty-four samples of Permian coal, partings, roof, and floor were collected from the Huaibei Coalfield, Anhui Province, China. Abundances of rare earth elements (REEs) and other elements in the samples were determined by inductively coupled-plasma mass spectrometry (ICP-MS) and inductively coupled-plasma atomic emission spectrometry (ICP-AES). The results show that the REEs are enriched in coals in the Huaibei Coalfield as compared with Chinese and U.S. coals and the world coal average. Coals in the Lower Shihezi Formation (No. 7, 5, and 4 Coals) and Upper Shihezi Formation (No. 3) have higher REE abundances than the coals in Shanxi Formation (No. 10). Magmatic intrusion resulted in high enrichment of REEs concentrations in No. 5 and 7 Coals. The REE abundances are positively correlated with the ash content. The mineral matter in these coals is mainly made up of clay minerals and carbonates. The REEs are positively correlated with lithophile elements including Si, Al, Ti, Fe, and Na, which are mainly distributed in clay minerals, indicating that REEs are contained mainly in clay minerals. The REE abundances in coals normalized by the ash are higher than that in partings. REEs abundances of coals cannot be accounted for by the REE content in the mineral matter, and some REEs associated with organic matter in coals. ?? 2007 Elsevier Ltd. All rights reserved.

  8. Scarcity of rare earth elements.

    PubMed

    de Boer, M A; Lammertsma, K

    2013-11-01

    Rare earth elements (REEs) are important for green and a large variety of high-tech technologies and are, therefore, in high demand. As a result, supply with REEs is likely to be disrupted (the degree of depends on the REE) in the near future. The 17 REEs are divided into heavy and light REEs. Other critical elements besides REEs, identified by the European Commission, are also becoming less easily available. Although there is no deficiency in the earth's crust of rare earth oxides, the economic accessibility is limited. The increased demand for REEs, the decreasing export from China, and geopolitical concerns on availability contributed to the (re)opening of mines in Australia and the USA and other mines are slow to follow. As a result, short supply of particularly terbium, dysprosium, praseodymium, and neodymium is expected to be problematic for at least the short term, also because they cannot be substituted. Recycling REEs from electronic waste would be a solution, but so far there are hardly any established REE recycling methods. Decreasing the dependency on REEs, for example, by identifying possible replacements or increasing their efficient use, represents another possibility. PMID:24009098

  9. Steric hindrance and the enhanced stability of light rare-earth elements in hydrothermal fluids

    SciTech Connect

    Mayanovic, Robert A.; Anderson, Alan J.; Bassett, William A.; Chou, I-Ming

    2009-10-05

    A series of X-ray absorption spectroscopy (XAS) experiments were made to determine the structure and stability of aqueous REE (La, Nd, Gd, and Yb) chloride complexes to 500 C and 520 MPa. The REE{sup 3+} ions exhibit inner-sphere chloroaqua complexation with a steady increase of chloride coordination with increasing temperature in the 150 to 500 C range. Furthermore, the degree of chloride coordination of REE{sup 3+} inner-sphere chloroaqua complexes decreases significantly from light to heavy REE. These results indicate that steric hindrance drives the reduction of chloride coordination of REE{sup 3+} inner-sphere chloroaqua complexes from light to heavy REE. This results in greater stability and preferential transport of light REE{sup 3+} over heavy REE{sup 3+} ions in saline hydrothermal fluids. Accordingly, the preferential mobility of light REE directly influences the relative abundance of REE in rocks and minerals and thus needs to be considered in geochemical modeling of petrogenetic and ore-forming processes affected by chloride-bearing hydrothermal fluids.

  10. Accumulation and fractionation of rare earth elements in atmospheric particulates around a mine tailing in Baotou, China

    NASA Astrophysics Data System (ADS)

    Wang, Lingqing; Liang, Tao

    2014-05-01

    Rare earth elements (REEs) have been increasingly emitted into the atmosphere with a worldwide increase in use of these metals. However, the research on REEs in atmospheric particulates is fairly limited. In this paper, atmospheric particulates including total suspended particulate (TSP) matter and particles with an equivalent aerodynamic diameter less than 10 μm (PM10) were collected around a rare earth mine tailing in Baotou, the largest rare earth industrial base in China, in August 2012 and March 2013, for the analyses of REE levels and distributions. The total concentrations of REEs for TSP were 172.91 and 297.49 ng/m3, and those for PM10 were 63.23 and 105.52 ng/m3, in August 2012 and March 2013, respectively. Enrichment factors for all 14 analyzed REEs in the TSP and PM10 indicated that the REE enrichment in atmosphere particulates was caused by anthropogenic sources and influenced by the strong wind in spring season. The spatial distribution of REEs in TSP showed a strong gradient in the prevailing wind direction. The chondrite-normalized patterns of REEs in TSP and PM10 were similar with the conspicuous fractionation between light REEs and heavy REEs.

  11. Rare earth elements in sediments of the Vigo Ria, NW Iberian Peninsula

    NASA Astrophysics Data System (ADS)

    Prego, Ricardo; Caetano, Miguel; Vale, Carlos; Marmolejo-Rodríguez, Judith

    2009-04-01

    The abundance and distribution of rare earth elements (REE) and their signatures in the Vigo Ria were studied from 50 samples of surface sediments and related to the geological formation in its watershed. The total amount of REE in the Ria is heterogeneous. It ranges from 220 mg kg -1 in the southern middle Ria margin in the vicinity of the Galiñeiro geological shore complex, which contains REE-enriched minerals, to 2 mg kg -1 near the Ria mouth due to dilution with high levels of carbonated biogenic particles (31% of Ca). Rare earth elements of the Ria sediments are considerably enriched in light-REE relative to heavy-REE (a LREE/HREE ratio of 9.7±1.6) and also show a slightly negative Eu-anomaly. Low European shale normalised REE patterns were distinguished in the innermost sediments of Vigo Ria, but were not correlated with Al. This suggests a minor contribution of REE from upstream freshwater inputs to the sediments in the middle Vigo Ria zone. Normalised REE ratios in the middle Ria imply that fine particles enriched in REE may be exported from the Ria to shelf mud patches and REE can be useful as sediment tracers of Ria input on the shelf.

  12. The geochemistry of rare earth elements in the Amazon River estuary

    SciTech Connect

    Shokovitz, E.R. )

    1993-05-01

    The estuarine geochemistry of rare earth elements (REEs) was studied using samples collected in the Amazon River estuary from the AmasSeds (Amazon Shelf SEDiment Study) cruise of August 1989. Extensive removal of dissolved (0.22 [mu]m filtered) trivalent REEs from river water occurs in the low (0--6) salinity region. Removal by the salt-induced coagulation of river colloids leads to fractionation among the REE(III) series; the order of removal is light REEs > middle REEs > heavy REEs. There also is the enhanced removal of Ce (relative to trivalent La and Nd) in the low salinity (0--6) zone and in the zone of high biological activity. This is the first field observation of strong Ce removal associated with coagulation of river colloids and biological productivity. The argument is made that the decrease in the Ce anomaly across a biological front is caused by biologically mediated oxidation of Ce(III) to Ce(IV). Coagulation of river colloids and biologically mediated oxidation of Ce(III) lead to fractionation of REE(III) and redox modification of Ce. These processes result in the REE composition becoming fractionated relative to the Amazon River water and crust and more evolved toward the REE composition of the oceans. This study implies that reactions in estuaries play significant, yet poorly understood roles in controlling the REE composition and Ce anomaly of the oceans. 46 refs., 9 figs., 2 tabs.

  13. An Appraisal of Endmember Energy and Mixing Properties of Rare Earth Garnets

    NASA Astrophysics Data System (ADS)

    Moretti, R.; Ottonello, G.

    1998-04-01

    The thermodynamic properties of rare earth aluminum (REE 3Al 5O 12), iron (REE 3Fe 5O 12), and gallium (REE 3Ga 5O 12) garnets are assessed by means of critical evaluation of the existing experimental data and thermodynamic treatment of their vibrational, static and volumetric properties. The mixing properties of the various REE garnet components are calculated from these endmember thermodynamic data and the interionic static potential model developed earlier for major silicate garnet components. These results permit evaluation of the solubility behavior for REE in natural phases. The results suggest that the mixing of REE garnet components at trace level (i.e., below about 10 2 ppm) with major silicate garnet components is virtually ideal, but strong positive deviations, associated with generalized polyhedral distortion of the host phase at higher concentration level of the solute, prevent bulk REE solubility from exceeding a few hundreds ppm. The computed rare earth element fractionations between garnet and supercritical fluid at various P, T conditions put in evidence the main control operated by the intrinsic energy properties of REE-garnet end members in determining the light REE/heavy REE (LREE/HREE) fractionation observed in natural garnet specimens.

  14. Energy Expenditure and Caloric Balance After Burn

    PubMed Central

    Hart, David W.; Wolf, Steven E.; Herndon, David N.; Chinkes, David L.; Lal, Sophia O.; Obeng, Michael K.; Beauford, Robert B.; Mlcak RT, Ronald P.

    2002-01-01

    Objective Resting energy expenditure (REE) is commonly measured in critical illness to determine caloric “demands” and thus nutritive needs. Summary Background Data The purpose of this study was to 1) determine whether REE is associated with clinical outcomes and 2) determine whether an optimal caloric delivery rate based on REE exists to offset erosion of lean mass after burn. Methods From 1995 to 2001, REE was measured by indirect calorimetry in 250 survivors of 10 to 99%TBSA burns. Caloric intake and REE were correlated with muscle protein catabolism, length of stay, ventilator dependence, sepsis, and mortality. From 1998 to 2000, 42 patients (>60%TBSA burns) received continuous enteral nutrition at a spectrum of caloric balance between 1.0x REE kcal/d –1.8x REE kcal/d. Serial body composition was measured by dual energy x-ray absorptiometry. Lean mass, fat mass, morbidity, and mortality were determined. Results REE/predicted basal metabolic rate correlated directly with burn size, sepsis, ventilator dependence, and muscle protein catabolism (P < .05). Declining REE correlated with mortality (P < .05). 2) Erosion of lean body mass was not attenuated by increased caloric balance, however, fat mass increased with caloric supply (P < .05). Conclusion In surviving burned patients, caloric delivery beyond 1.2 × REE results in increased fat mass without changes in lean body mass. Declining energy expenditure appears to be a harbinger of mortality in severely burned patients. PMID:11753055

  15. Effects of a caspase and a calpain inhibitor on resting energy expenditures in normal and hypermetabolic rats: a pilot study.

    PubMed

    Vana, P G; LaPorte, H M; Kennedy, R H; Gamelli, R L; Majetschak, M

    2016-07-18

    Several diseases induce hypermetabolism, which is characterized by increases in resting energy expenditures (REE) and whole body protein loss. Exaggerated protein degradation is thought to be the driving force underlying this response. The effects of caspase and calpain inhibitors on REE in physiological and hypermetabolic conditions, however, are unknown. Thus, we studied whether MDL28170 (calpain inhibitor) or z-VAD-fmk (caspase inhibitor) affect REE under physiological conditions and during hypermetabolism post-burn. Rats were treated five times weekly and observed for 6 weeks. Treatment was started 2 h (early) or 48 h (late) after burn. In normal rats, MDL28170 transiently increased REE to 130 % of normal during week 2-4. z-VAD-fmk reduced REE by 20-25 % throughout the observation period. Within 14 days after burns, REE increased to 130+/-5 %. Whereas MDL28170/early treatment did not affect REE, MDL28170/late transiently increased REE to 180+/-10 % of normal by week 4 post-burn. In contrast, with z-VAD-fmk/early REE remained between 90-110 % of normal post-burn. z-VAD-fmk/late did not affect burn-induced increases in REE. These data suggest that caspase cascades contribute to the development of hypermetabolism and that burn-induced hypermetabolism can be pharmacologically modulated. Our data point towards caspase cascades as possible therapeutic targets to attenuate hypermetabolism after burns, and possibly in other catabolic disease processes. PMID:27070748

  16. Effects of spraying rare earths on contents of rare Earth elements and effective components in tea.

    PubMed

    Wang, Dongfeng; Wang, Changhong; Ye, Sheng; Qi, Hongtao; Zhao, Guiwen

    2003-11-01

    Rare earth (RE) fertilizer is widely applied in China to increase the yield and the quality of crops including tea. However, the effects of spraying RE fertilizer on the contents of rare earth elements (REE) and effective components in tea are unknown. The results from basin and field experiments show that the values of the REE concentrations in new shoots of tea plants and the concentration of REE in the soil (REE/REEs) either from control basins or from treatment basins were smaller than those in other parts of tea plant and similar between control and treatment. The longer the interval between spraying RE fertilizer and picking the shoots of tea plants, the less the effects from spraying. About 80% summation operator REE (the sum of the concentrations of 15 REE) in tea, whether it came from spraying or not, was insoluble in the infusion. About 10% the soluble REE of summation operator REE in tea infusion was bound to polysaccharide, and the amount of REE bound polysaccharide decreased over time. At least a 25 day safety interval is needed between spraying and picking if the microelement fertilizer is used, in order to enhance tea output and to ensure tea safety. PMID:14582968

  17. Rare earth patterns in shergottite phosphates and residues

    NASA Technical Reports Server (NTRS)

    Laul, J. C.

    1987-01-01

    Leaching experiments with 1M HCl on ALHA 77005 powder show that rare earth elements (REE) are concentrated in accessory phosphate phases (whitlockite, apatite) that govern the REE patterns of bulk shergottites. The REE patterns of whitlockite are typically light REE-depleted with a negative Eu anomaly and show a hump at the heavy REE side, while the REE pattern of apatite (in Shergotty) is light REE-enriched. Parent magmas are calculated from the modal compositions of residues of ALHA 77005, Shergotty, and EETA 79001. The parent magmas lack a Eu anomaly, indicating that plagioclase was a late-stage crystallizing phase and that it probably crystallized before the phosphates. The parent magmas of ALHA 77005 and Shergotty have similar REE patterns, with a subchondritic Nd/Sm ratio. However, the Sm/Nd isotopoics require a light REE-depleted source for ALHA 77005 (if the crystallization age is less than 600 Myr) and a light REE-enriched source for Shergotty. Distant Nd and Sr isotopic signatures may suggest different source regions for shergottites.

  18. An Experimental Study on Using Rare Earth Elements to Trace Non-point source Phosphorous LossA

    NASA Astrophysics Data System (ADS)

    Liang, T.

    2011-12-01

    Controlling phosphorous (P) inputs through management of its sources and transport is critical for limiting freshwater eutrophication. Rare earth elements (REEs) have been successfully used in the analysis of soil erosion and pollutant sources, as well as in the analysis of mineral genesis. To better understand the potential for REE use in tracing non-point sources of P, we examined the combined fate of REEs and P in Chinese soils amended with REEs and documented the formation of REE-P compounds. Laboratory leaching experiments and artificial simulated rainfall experiments were conducted. Vertical leaching transfers of REEs and P were relatively small, with transport depths less than 6 cm for most REEs and P. Export of applied REEs in leachate accounted for less that 5% of inputs. The vertical mobility order of REEs and P in Chinese soils was greatest for purple soil, followed by terra nera soil, then red soil, followed by cinnamon soil, and finally loess soil. Losses of rare earth elements and P in surface runoff exhibited a parabolic relationship to simulated rainfall intensity. With greater exogenous La application, the amount of water soluble P, bicarbonate-extractable P and hydroxide-extractable P decreased significantly, while acid-extractable and residual forms of P increased significantly. In addition, characteristics of exogenous rare earth elements (REEs) and P and their losses with surface runoff (both in the water and sediments) during simulated rainfall experiments (83 mm h-1) were investigated. The results revealed that most REEs (La, 94%; Nd, 93%; Sm, 96%) and P (96%) transported with sediments in the runoff. The total amounts of losses of REEs and P in the runoff were significantly correlated, suggesting the possibility of using REEs to trace the fate of agricultural nonpoint P losses.

  19. Rare Earth Element Partitioning in Lunar Minerals: An Experimental Study

    NASA Technical Reports Server (NTRS)

    McIntosh, E. C.; Rapp, J. F.; Draper, D. S.

    2016-01-01

    The partitioning behavior of rare earth elements (REE) between minerals and melts is widely used to interpret the petrogenesis and geologic context of terrestrial and extra-terrestrial samples. REE are important tools for modelling the evolution of the lunar interior. The ubiquitous negative Eu anomaly in lunar basalts is one of the main lines of evidence to support the lunar magma ocean (LMO) hypothesis, by which the plagioclase-rich lunar highlands were formed as a flotation crust during differentiation of a global-scale magma ocean. The separation of plagioclase from the mafic cumulates is thought to be the source of the Eu depletion, as Eu is very compatible in plagioclase. Lunar basalts and volcanic glasses are commonly depleted in light REEs (LREE), and more enriched in heavy REEs (HREE). However, there is very little experimental data available on REE partitioning between lunar minerals and melts. In order to interpret the source of these distinctive REE patterns, and to model lunar petrogenetic processes, REE partition coefficients (D) between lunar minerals and melts are needed at conditions relevant to lunar processes. New data on D(sub REE) for plagioclase, and pyroxenes are now available, but there is limited available data for olivine/melt D(sub REE), particularly at pressures higher than 1 bar, and in Fe-rich and reduced compositions - all conditions relevant to the lunar mantle. Based on terrestrial data, REE are highly incompatible in olivine (i.e. D much less than 1), however olivine is the predominant mineral in the lunar interior, so it is important to understand whether it is capable of storing even small amounts of REE, and how the REEs might be fractionatied, in order to understand the trace element budget of the lunar interior. This abstract presents results from high-pressure and temperature experiments investigating REE partitioning between olivine and melt in a composition relevant to lunar magmatism.

  20. LA-ICP-MS of rare earth elements concentrated in cation-exchange resin particles for origin attribution of uranium ore concentrate.

    PubMed

    Asai, Shiho; Limbeck, Andreas

    2015-04-01

    Rare earth elements (REE) concentrated on cation-exchange resin particles were measured with laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to obtain chondrite-normalized REE plots. The sensitivity of REE increased in ascending order of the atomic number, according to the sensitivity trend in pneumatic nebulization ICP-MS (PN-ICP-MS). The signal intensities of REE were nearly proportional to the concentrations of REE in the immersion solution used for particle-preparation. Minimum measurable concentration calculated from the net signals of REE was approximately 1 ng/g corresponding to 0.1 ng in the particle-preparation solution. In LA analysis, formation of oxide and hydroxide of the light REE and Ba which causes spectral interferences in the heavy REE measurement was effectively attenuated due to the solvent-free measurement capability, compared to conventional PN-ICP-MS. To evaluate the applicability of the proposed method, the REE-adsorbed particles prepared by immersing them in a U-bearing solution (commercially available U standard solution) were measured with LA-ICP-MS. Aside from the LA analysis, each concentration of REE in the same U standard solution was determined with conventional PN-ICP-MS after separating REE by cation-exchange chromatography. The concentrations of REE were ranging from 0.04 (Pr) to 1.08 (Dy) μg/g-U. The chondrite-normalized plot obtained through LA-ICP-MS analysis of the U standard sample exhibited close agreement with that obtained through the PN-ICP-MS of the REE-separated solution within the uncertainties. PMID:25640124

  1. Trends in the Rare Earth Element Content of U.S.-Based Coal Combustion Fly Ashes.

    PubMed

    Taggart, Ross K; Hower, James C; Dwyer, Gary S; Hsu-Kim, Heileen

    2016-06-01

    Rare earth elements (REEs) are critical and strategic materials in the defense, energy, electronics, and automotive industries. The reclamation of REEs from coal combustion fly ash has been proposed as a way to supplement REE mining. However, the typical REE contents in coal fly ash, particularly in the United States, have not been comprehensively documented or compared among the major types of coal feedstocks that determine fly ash composition. The objective of this study was to characterize a broad selection of U.S. fly ashes of varied geological origin in order to rank their potential for REE recovery. The total and nitric acid-extractable REE content for more than 100 ash samples were correlated with characteristics such as the major element content and coal basin to elucidate trends in REE enrichment. Average total REE content (defined as the sum of the lanthanides, yttrium, and scandium) for ashes derived from Appalachian sources was 591 mg kg(-1) and significantly greater than in ashes from Illinois and Powder River basin coals (403 and 337 mg kg(-1), respectively). The fraction of critical REEs (Nd, Eu, Tb, Dy, Y, and Er) in the fly ashes was 34-38% of the total and considerably higher than in conventional ores (typically less than 15%). Powder River Basin ashes had the highest extractable REE content, with 70% of the total REE recovered by heated nitric acid digestion. This is likely due to the higher calcium content of Powder River Basin ashes, which enhances their solubility in nitric acid. Sc, Nd, and Dy were the major contributors to the total REE value in fly ash, based on their contents and recent market prices. Overall, this study shows that coal fly ash production could provide a substantial domestic supply of REEs, but the feasibility of recovery depends on the development of extraction technologies that could be tailored to the major mineral content and origins of the feed coal for the ash. PMID:27228215

  2. The effect of diagenesis and fluid migration on rare earth element distribution in pore fluids of the northern Cascadia accretionary margin

    USGS Publications Warehouse

    Kim, Ji-Hoon; Torres, Marta E.; Haley, Brian A.; Kastner, Miriam; Pohlman, John W.; Riedel, Michael; Lee, Young-Joo

    2012-01-01

    Analytical challenges in obtaining high quality measurements of rare earth elements (REEs) from small pore fluid volumes have limited the application of REEs as deep fluid geochemical tracers. Using a recently developed analytical technique, we analyzed REEs from pore fluids collected from Sites U1325 and U1329, drilled on the northern Cascadia margin during the Integrated Ocean Drilling Program (IODP) Expedition 311, to investigate the REE behavior during diagenesis and their utility as tracers of deep fluid migration. These sites were selected because they represent contrasting settings on an accretionary margin: a ponded basin at the toe of the margin, and the landward Tofino Basin near the shelf's edge. REE concentrations of pore fluid in the methanogenic zone at Sites U1325 and U1329 correlate positively with concentrations of dissolved organic carbon (DOC) and alkalinity. Fractionations across the REE series are driven by preferential complexation of the heavy REEs. Simultaneous enrichment of diagenetic indicators (DOC and alkalinity) and of REEs (in particular the heavy elements Ho to Lu), suggests that the heavy REEs are released during particulate organic carbon (POC) degradation and are subsequently chelated by DOC. REE concentrations are greater at Site U1325, a site where shorter residence times of POC in sulfate-bearing redox zones may enhance REE burial efficiency within sulfidic and methanogenic sediment zones where REE release ensues. Cross-plots of La concentrations versus Cl, Li and Sr delineate a distinct field for the deep fluids (z > 75 mbsf) at Site U1329, and indicate the presence of a fluid not observed at the other sites drilled on the Cascadia margin. Changes in REE patterns, the presence of a positive Eu anomaly, and other available geochemical data for this site suggest a complex hydrology and possible interaction with the igneous Crescent Terrane, located east of the drilled transect.

  3. Rare earth and trace elements of fossil vertebrate bioapatite as palaeoenvironmental and sedimentological proxies

    NASA Astrophysics Data System (ADS)

    Žigaitė, Živilė; Fadel, Alexandre; Pérez-Huerta, Alberto; Jeffries, Teresa

    2015-04-01

    Rare earth (REE) and trace element compositions of fossil vertebrate dental microremains have been studied in Silurian and Devonian vertebrate dental scales and spines in-situ, using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). Samples were selected from the well-known Silurian bone beds of Vesiku and Ohesaare in Saaremaa island of Estonia, and a number of Lower Devonian localities from Spitsbergen (Svalbard), Andrée Land group. Biomineral preservation was assessed using spot semi-quantitative elemental chemistry (SEM-EDS) and electron back-scatter difractometry (EBSD) for cristallinity imaging. The obtained PAAS shale-normalised REE concentrations were evaluated using basic geochemical calculations and quantifications. The REE patterns from the Lower Devonian vertebrate apatite from Andrée Land, Spitsbergen (Wood Bay and Grey Hœk formations) did not show any recognisable taxon-specific behavior, but had rather well expressed differences of REE compositions related to biomineral structure and sedimentary settings, suggesting REE instead to reflect burial environments and sedimentological history. The Eu anomaly recorded in two of the studied localities but not in the other indicate different taphonomic conditions and palaeoenvironment, while La/Sm, La/Yb ratios sugeest considerable influence of terrestrial freshwater during the early diagenesis. The La/Yb and La/Sm plots also agree with the average REE concentrations, reflecting domination of the adsoption over substitution as principal REE uptake mechanism in the fossils which had significantly lower overall REE concentrations, and vice versa. Vesiku (Homerian, Wenlock) microremains yielded very uniform REE patterns with slightly lower overall REE concentrations in enameloid than in dentine, with strong enrichment in middle REE and depletion in heavy REE. Negative Europium (Eu) anomaly was pronounced in all the profiles, but Cerium (Ce) anomalies were not detected suggesting possible

  4. Mesosiderite clasts with the most extreme positive europium anomalies among solar system rocks

    NASA Technical Reports Server (NTRS)

    Mittlefehldt, David W.; Rubin, Alan E.; Davis, Andrew M.

    1992-01-01

    Pigeonite-plagioclase gabbros that occur as clasts in mesosiderites (brecciated stony-iron meteorites) show extreme fractionations of the rare-earth elements (REEs) with larger positive europium anomalies than any previously known for igneous rocks from the earth, moon, or meteorite parent bodies and greater depletions of light REEs relative to heavy REEs than known for comparable cumulate gabbros. The REE pattern for merrillite in one of these clasts is depleted in light REEs and has a large positive europium anomaly as a result of metamorphic equilibration with the silicates. The extreme REE ratios exhibited by the mesosiderite clasts demonstrate that multistage igneous processes must have occurred on some asteroids in the early solar system. Melting of the crust by large-scale impacts or electrical induction from an early T-Tauri-phase sun may be responsible for these processes.

  5. Ligand extraction of rare earth elements from aquifer sediments: Implications for rare earth element complexation with organic matter in natural waters

    NASA Astrophysics Data System (ADS)

    Tang, Jianwu; Johannesson, Karen H.

    2010-12-01

    The ability of organic matter as well as carbonate ions to extract rare earth elements (REEs) from sandy sediments of a Coastal Plain aquifer was investigated for unpurified organic matter from different sources (i.e., Mississippi River natural organic matter, Aldrich humic acid, Nordic aquatic fulvic acid, Suwannee River fulvic acid, and Suwannee River natural organic matter) and for extraction solutions containing weak (i.e., CH 3COO -) or strong (i.e., CO32-) ligands. The experimental results indicate that, in the absence of strong REE complexing ligands in solution, the amount of REEs released from the sand is small and the fractionation pattern of the released REEs appears to be controlled by the surface stability constants for REE sorption with Fe(III) oxides/oxyhydroxides. In the presence of strong solution complexing ligands, however, the amount and the fractionation pattern of the released REEs reflect the strength and variation of the stability constants of the dominant aqueous REE species across the REE series. The varying amount of REEs extracted by the different organic matter employed in the experiments indicates that organic matter from different sources has different complexing capacity for REEs. However, the fractionation pattern of REEs extracted by the various organic matter used in our experiments is remarkable consistent, being independent of the source and the concentration of organic matter used, as well as solution pH. Because natural aquifer sand and unpurified organic matter were used in our experiments, our experimental conditions are more broadly similar to natural systems than many previous laboratory experiments of REE-humic complexation that employed purified humic substances. Our results suggest that the REE loading effect on REE-humic complexation is negligible in natural waters as more abundant metal cations (e.g., Fe, Al) out-compete REEs for strong binding sites on organic matter. More specifically, our results indicate that REE

  6. Rare earth elements in river waters

    NASA Technical Reports Server (NTRS)

    Goldstein, Steven J.; Jacobsen, Stein B.

    1988-01-01

    To characterize the input to the oceans of rare earth elements (REE) in the dissolved and the suspended loads of rivers, the REE concentrations were measured in samples of Amazon, Indus, Mississippi, Murray-Darling, and Ohio rivers and in samples of smaller rivers that had more distinct drainage basin lithology and water chemistry. It was found that, in the suspended loads of small rivers, the REE pattern was dependent on drainage basin geology, whereas the suspended loads in major rivers had relatively uniform REE patterns and were heavy-REE depleted relative to the North American Shale composite (NASC). The dissolved loads in the five major rivers had marked relative heavy-REE enrichments, relative to the NASC and the suspended material, with the (La/Yb)N ratio of about 0.4 (as compared with the ratio of about 1.9 in suspended loads).

  7. Rare earth elements minimal harvest year variation facilitates robust geographical origin discrimination: The case of PDO "Fava Santorinis".

    PubMed

    Drivelos, Spiros A; Danezis, Georgios P; Haroutounian, Serkos A; Georgiou, Constantinos A

    2016-12-15

    This study examines the trace and rare earth elemental (REE) fingerprint variations of PDO (Protected Designation of Origin) "Fava Santorinis" over three consecutive harvesting years (2011-2013). Classification of samples in harvesting years was studied by performing discriminant analysis (DA), k nearest neighbours (κ-NN), partial least squares (PLS) analysis and probabilistic neural networks (PNN) using rare earth elements and trace metals determined using ICP-MS. DA performed better than κ-NN, producing 100% discrimination using trace elements and 79% using REEs. PLS was found to be superior to PNN, achieving 99% and 90% classification for trace and REEs, respectively, while PNN achieved 96% and 71% classification for trace and REEs, respectively. The information obtained using REEs did not enhance classification, indicating that REEs vary minimally per harvesting year, providing robust geographical origin discrimination. The results show that seasonal patterns can occur in the elemental composition of "Fava Santorinis", probably reflecting seasonality of climate. PMID:27451177

  8. Magnesian anorthosites and associated troctolites and dunite in Apollo 14 breccias

    NASA Technical Reports Server (NTRS)

    Lindstrom, M. M.; Knapp, S. A.; Shervais, J. W.; Taylor, L. A.

    1984-01-01

    Magnesian anorthosite, a new type of pristine lunar highlands rock, has been found in Apollo 14 breccias. It has primitive (high Ca and Mg) silicate mineral compositions, and high and variable REE concentrations. Variations in REE contents can be accounted for by variations in modal abundance of REE-rich apatite. Magnesian anorthosites are associated with troctolites and a dunite with very similar mineral compositions and it is suggested that all crystallized from a differentiated troctolitic intrusion. The origin of the REE-rich apatite is enigmatic. It is unlikely to have crystallized from an igneous liquid in equilibrium with the major minerals in the anorthosite. Possible origins are assimilation of urKREEP or metasomatism by REE-rich fluids. REE-rich alkali anorthosites and gabbronorites are also found and are likely to be related to KREEP basalt magmas. Lunar compositional associations are distributed in a regional rather than global manner.

  9. Global demand for rare earth resources and strategies for green mining.

    PubMed

    Dutta, Tanushree; Kim, Ki-Hyun; Uchimiya, Minori; Kwon, Eilhann E; Jeon, Byong-Hun; Deep, Akash; Yun, Seong-Taek

    2016-10-01

    Rare earth elements (REEs) are essential raw materials for emerging renewable energy resources and 'smart' electronic devices. Global REE demand is slated to grow at an annual rate of 5% by 2020. This high growth rate will require a steady supply base of REEs in the long run. At present, China is responsible for 85% of global rare earth oxide (REO) production. To overcome this monopolistic supply situation, new strategies and investments are necessary to satisfy domestic supply demands. Concurrently, environmental, economic, and social problems arising from REE mining must be addressed. There is an urgent need to develop efficient REE recycling techniques from end-of-life products, technologies to minimize the amount of REEs required per unit device, and methods to recover them from fly ash or fossil fuel-burning wastes. PMID:27295408

  10. Magnesian anorthosites and associated troctolites and dunite in Apollo 14 breccias

    SciTech Connect

    Lindstrom, M.M.; Knapp, S.A.

    1984-11-15

    Magnesian anorthosite, a new type of pristine lunar highlands rock, has been found in Apollo 14 breccias. It has primitive (high Ca and Mg) silicate mineral compositions, and high and variable REE concentrations. Variations in REE contents can be accounted for by variations in modal abundance of REE-rich apatite. Magnesian anorthosites are associated with troctolites and a dunite with very similar mineral compositions and it is suggested that all crystallized from a differentiated troctolitic intrusion. The origin of the REE-rich apatite is enigmatic. It is unlikely to have crystallized from an igneous liquid in equilibrium with the major minerals in the anorthosite. Possible origins are assimilation of urKREEP or metasomatism by REE-rich fluids. REE-rich alkali anorthosites and gabbronorites are also found and are likely to be related to KREEP basalt magmas. Lunar compositional associations are distributed in a regional rather than global manner.

  11. Rare earth element systematics in hydrothermal fluids

    SciTech Connect

    Michard, A. )

    1989-03-01

    Rare earth element concentrations have been measured in hydrothermal solutions from geothermal fields in Italy, Dominica, Valles Caldera, Salton Sea and the Mid-Atlantic Ridge. The measured abundances show that hydrothermal activity is not expected to affect the REE balance of either continental or oceanic rocks. The REE enrichment of the solutions increases when the pH decreases. High-temperature solutions (> 230{degree}C) percolating through different rock types may show similar REE patterns.

  12. Critical Zone Weathering and Your Smartphone: Understanding How Mineral Decomposition and Colloid Redistribution Can Generate Rare Earth Element Deposits

    NASA Astrophysics Data System (ADS)

    Bern, C.; Foley, N.

    2014-12-01

    Rare earth elements (REE's) are crucial in the manufacture of smartphones and many other high tech devices. Increasing global demand and relatively narrow geographic sourcing have promoted interest in understanding REE deposit genesis and distribution. Highly weathered, clay-hosted, ion-exchange type deposits in southern China are the source of much of the world's production of the more valuable heavy REEs. Such deposits form as REE-bearing minerals weather and REEs released to solution in ionic form are retained by negatively charged exchange sites on clay minerals. We are investigating the potential for ion-exchange REE deposits in the Piedmont of the southeastern United States, where slow erosion rates have preserved thick (up to 20 m) regolith, as required for such deposits. The Liberty Hill pluton outcrops as coarse-grained biotite-amphibole granite and quartz monzonite over nearly 400 km2 in South Carolina, and has an age of 305 Ma (new SHRIMP ion microprobe zircon age). In weathered profiles over the pluton, ion-exchangeable REE content ranges from 8 to 580 ppm and accounts for 2 to 80% of bulk REE content. Elemental and heavy mineral distributions suggest the wide ranging differences in leachability may be attributable to the amount and distribution of resistant REE-bearing phases (e.g., monazite) relative to more easily weathered phases (e.g., allanite) in the parent granite. The REEs show little mobility within the regolith, indicating the effectiveness of the ion-exchange retention mechanism. In contrast, vertical redistribution of colloidal material shows maximum accumulations at ~1 m depth, as traced by the newly developed dual-phase (colloids vs. solution) mass balance model. The contrast suggests redistributed colloidal material has minimal influence on REE mobilization or retention. Conditions and processes necessary for ion-exchange REE deposit development exist in the Piedmont, but their presence will depend upon favorable parent rock mineralogy.

  13. Rare earth element systematics of fossil bone revealed by LA-ICPMS analysis

    NASA Astrophysics Data System (ADS)

    Herwartz, Daniel; Tütken, Thomas; Jochum, Klaus Peter; Sander, P. Martin

    2013-02-01

    Intra-bone rare earth element (REE) fractionation trends were studied by LA-ICPMS analysis to put constraints on (1) the mechanisms controlling REE fractionation within fossil bones; (2) the relative timing of REE uptake in various parts of fossil bone and (3) the origin of REE in fossil bones. We have evaluated REE bone profiles across 54 fossil bones from a broad range of well-characterised taphonomic settings ranging in age from Triassic to early Medieval. REE patterns and concentration gradients are highly variable and intra-bone fractionation trends in (La/Yb)N vs. (La/Sm)N space of few specimens cover almost the entire range previously observed for bulk samples. Intra-bone variability of Ce anomalies, as well as variable Y/Ho and (La/La∗)N is also observed. Sometimes, diagenetic fluids with fractionated, HREE enriched compositions have entered the bone from the marrow cavity, producing secondary REE uptake profiles. Theoretical intra-bone fractionation trends, modelled using lattice strain theory, concur with most REE data but some trends cannot be modelled using realistic boundary conditions. This fact, as well as the occurence of positive and negative Ce anomalies within the same fossil sample, hint towards changing REE compositions of diagenetic fluids over the timescales of REE uptake. Because apparent Ce anomalies frequently evolve over bone profiles and Ce anomalies can be inherited from previous fractionation events, Ce anomalies are a highly ambiguous tracer for constraining ambient redox conditions. In general, bioapatite REE signatures may not always reliably reflect ambient taphonomic or redox conditions and diagenetic fluid compositions. Therefore REE patterns and Ce anomalies of fossil bones must be interpreted cautiously as they vary spatially within skeletal remains and are affected by intra-bone fractionation processes as well as changing compositions of the diagenetic fluid.

  14. Rare earth element concentrations in geological and synthetic samples using synchrotron X-ray fluorescence analysis

    USGS Publications Warehouse

    Chen, J.R.; Chao, E.C.T.; Back, J.M.; Minkin, J.A.; Rivers, M.L.; Sutton, S.R.; Cygan, G.L.; Grossman, J.N.; Reed, M.J.

    1993-01-01

    The concentrations of rare earth elements (REEs) in specific mineral grains from the Bayan Obo ore deposit and synthetic high-silica glass samples have been measured by synchrotron X-ray fluorescence (SXRF) analysis using excitation of the REE K lines between 33 and 63 keV. Because SXRF, a nondestructive analytical technique, has much lower minimum detection limits (MDLs) for REEs, it is an important device that extends the in situ analytical capability of electron probe microanalysis (EPMA). The distribution of trace amounts of REEs in common rock-forming minerals, as well as in REE minerals and minerals having minor quantities of REEs, can be analyzed with SXRF. Synchrotron radiation from a bending magnet and a wiggler source at the National Synchrotron Light Source, Brookhaven National Laboratory, was used to excite the REEs. MDLs of 6 ppm (La) to 26 ppm (Lu) for 3600 s in 60-??m-thick standard samples were obtained with a 25-??m diameter wiggler beam. The MDLs for the light REEs were a factor of 10-20 lower than the MDLs obtained with a bending magnet beam. The SXRF REE concentrations in mineral grains greater than 25 ??m compared favorably with measurements using EPMA. Because EPMA offered REE MDLs as low as several hundred ppm, the comparison was limited to the abundant light REEs (La, Ce, Pr, Nd). For trace values of medium and heavy REEs, the SXRF concentrations were in good agreement with measurements using instrumental neutron activation analysis (INAA), a bulk analysis technique. ?? 1993.

  15. Rare earth element geochemistry of acid-sulphate and acid-sulphate-chloride geothermal systems from Yellowstone National Park, Wyoming, USA

    SciTech Connect

    Lewis, A.J.; Palmer, M.R.; Kemp, A.J.; Sturchio, N.C.

    1997-02-01

    Rare earth element (REE) concentrations have been determined by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) in acid-sulphate and acid-sulphate-chloride waters and the associated sinters and volcanic rocks from the Yellowstone National Park (YNP), Wyoming, USA, geothermal system. REE concentrations in the volcanic rocks range from 222 to 347 ppm: their chondrite-normalised REE patterns are typical of upper continental crust, with LREE > HREE and negative Eu anomalies. Total REE concentrations in the fluids range from 3 to 1133 nmol kg{sup -1} ({ge}162 ppm), and {Sigma}REE concentrations in sinter are {ge}181 ppm. REE abundances and patterns in drill core material from YNP indicate some REE mobility. Relative to the host rocks the REE patterns of the fluids are variably depleted in HREEs and LREEs, and usually have a pronounced positive Eu anomaly. This decoupling of Eu from the REE suite suggests that (1) Eu has been preferentially removed either from the host rock glass or from the host rock minerals, or (2) the waters are from a high temperature or reducing environment where Eu{sup 2+} is more soluble than the trivalent REEs. Since the latter is inconsistent with production of acid-sulphate springs in a low temperature, oxidising near-surface environment, we suggest that the positive Eu anomalies in the fluids result from preferential dissolution of a Eu-rich phase in the host rock. Spatial and temporal variations in major element chemistry and pH of the springs sampled from Norris Geyser Basin and Crater Hills accompany variations in REE concentrations and patterns of individual geothermal springs. These are possibly related to changes in subsurface plumbing, which results in variations in mixing and dilution of the geothermal fluids and may have lead to changes in the extent and nature of REE complexing. 37 refs., 7 figs., 4 tabs.

  16. Aluminium competitive effect on rare earth elements binding to humic acid

    NASA Astrophysics Data System (ADS)

    Marsac, Rémi; Davranche, Mélanie; Gruau, Gérard; Dia, Aline; Bouhnik-Le Coz, Martine

    2012-07-01

    Competitive mechanisms between rare earth elements (REE) and aluminium for humic acid (HA) binding were investigated by combining laboratory experiments and modeling to evaluate the effect of Al on REE-HA complexation. Results indicates that Al3+ competes more efficiently with heavy REE (HREE) than with light REE (LREE) in acidic (pH = 3) and low REE/HA concentration ratio conditions providing evidence for the Al high affinity for the few HA multidentate sites. Under higher pH - 5 to 6 - and high REE/HA conditions, Al is more competitive for LREE suggesting that Al is bound to HA carboxylic rather than phenolic sites. PHREEQC/Model VI Al-HA binding parameters were optimized to simulate precisely both Al binding to HA and Al competitive effect on REE binding to HA. REE-HA binding pattern is satisfactorily simulated for the whole experimental conditions by the ΔLK1A optimization (i.e. ΔLK1A controls the distribution width of log K around log KMA). The present study provides fundamental knowledge on Al binding mechanisms to HA. Aluminium competitive effect on other cations binding to HA depends clearly on its affinity for carboxylic, phenolic or chelate ligands, which is pH dependent. Under circumneutral pH such as in natural waters, Al should lead to LREE-depleted patterns since Al is expected to be bound to weak HA carboxylic groups. As deduced from the behavior of Al species, other potential competitor cations are expected to have their own competitive effect on REE-HA binding. Therefore, in order to reliably understand and model REE-HA patterns in natural waters, a precise knowledge of the exact behavior of the different REE competitor cations is required. Finally, this study highlights the ability of the REE to be used as a “speciation probe” to precisely describe cation interactions with HA as here evidenced for Al.

  17. The rare earth element potential of kaolin deposits in the Bohemian Massif (Czech Republic, Austria)

    NASA Astrophysics Data System (ADS)

    Höhn, S.; Frimmel, H. E.; Pašava, J.

    2014-12-01

    Four kaolin deposits in the Bohemian Massif were studied in order to assess the potential for the recovery of rare earth elements (REE) as by-products from the residue after extraction and refining of the raw kaolin. The behaviour of REE + Y during kaolinitization was found to be largely a function of pre-alteration mineralogy. In the examples studied, i.e. granite-derived deposits of Kriechbaum (Austria) and Božičany, and arkose-derived deposits of Kaznějov and Podbořany (all Czech Republic), the REE + Y are predominantly hosted by monazite which has remained unaffected by kaolinitization. The overall REE + Y content of the variably kaolinitized rocks is strongly dependent on their genesis. While ion adsorption plays only a minor role in the concentration of REE + Y in the studied kaolinitized rocks, the processing and refining of the raw kaolin leads to residues that are enriched in REE + Y by a factor of up to 40. The use of a magnetic separator and a hydrocyclone in the processing of the raw material can yield REE + Y contents of as much as 0.77 wt%. Although this value compares well with the REE + Y concentration in some potentially economic REE + Y projects elsewhere, the overall tonnage of the (REE + Y)-enriched residue is by far not sufficient to consider economic extraction of REE + Y as by-product. Our results are most probably applicable also to other kaolin deposits derived from the weathering of Hercynian basement granites elsewhere (e.g. in Saxonia and Bavaria, Germany). Overall, the potential for REE + Y production as by-product from kaolin mining has to be regarded as minimal.

  18. Rare earth element components in atmospheric particulates in the Bayan Obo mine region

    SciTech Connect

    Wang, Lingqing Liang, Tao Zhang, Qian; Li, Kexin

    2014-05-01

    The Bayan Obo mine, located in Inner Mongolia, China, is the largest light rare earth body ever found in the world. The research for rare earth elements (REEs) enrichment in atmospheric particulates caused by mining and ore processing is fairly limited so far. In this paper, atmospheric particulates including total suspended particulate (TSP) matter and particles with an equivalent aerodynamic diameter less than 10 μm (PM{sub 10}) were collected around the Bayan Obo mine region, in August 2012 and March 2013, to analyze the levels and distributions of REEs in particles. The total concentrations of REEs for TSP were 149.8 and 239.6 ng/m{sup 3}, and those for PM{sub 10} were 42.8 and 68.9 ng/m{sup 3}, in August 2012 and March 2013, respectively. Enrichment factor was calculated for all 14 REEs in the TSP and PM{sub 10} and the results indicated that REEs enrichment in atmosphere particulates was caused by anthropogenic sources and influenced by the strong wind in springtime. The spatial distribution of REEs in TSP showed a strong gradient concentration in the prevailing wind direction. REE chondrite normalized patterns of TSP and PM{sub 10} were similar and the normalized curves inclined to the right side, showing the conspicuous fractionation between the light REEs and heavy REE, which supported by the chondrite normalized concentration ratios calculated for selected elements (La{sub N}/Yb{sub N}, La{sub N}/Sm{sub N}, Gd{sub N}/Yb{sub N}). - Highlights: • TSP and PM{sub 10} samples were collected to analyze the levels and distributions of REE. • Enrichment factors indicated that REE enrichment was caused by anthropogenic sources. • The distribution of REEs showed a strong gradient in the prevailing wind direction. • Obvious fractionation between LREEs and HREEs is observed in atmospheric particulates.

  19. Predictive equations underestimate resting energy expenditure in female adolescents with phenylketonuria

    PubMed Central

    Quirk, Meghan E.; Schmotzer, Brian J.; Schmotzer, Brian J.; Singh, Rani H.

    2010-01-01

    Resting energy expenditure (REE) is often used to estimate total energy needs. The Schofield equation based on weight and height has been reported to underestimate REE in female children with phenylketonuria (PKU). The objective of this observational, cross-sectional study was to evaluate the agreement of measured REE with predicted REE for female adolescents with PKU. A total of 36 females (aged 11.5-18.7 years) with PKU attending Emory University’s Metabolic Camp (June 2002 – June 2008) underwent indirect calorimetry. Measured REE was compared to six predictive equations using paired Student’s t-tests, regression-based analysis, and assessment of clinical accuracy. The differences between measured and predicted REE were modeled against clinical parameters to determine to if a relationship existed. All six selected equations significantly under predicted measured REE (P< 0.005). The Schofield equation based on weight had the greatest level of agreement, with the lowest mean prediction bias (144 kcal) and highest concordance correlation coefficient (0.626). However, the Schofield equation based on weight lacked clinical accuracy, predicting measured REE within ±10% in only 14 of 36 participants. Clinical parameters were not associated with bias for any of the equations. Predictive equations underestimated measured REE in this group of female adolescents with PKU. Currently, there is no accurate and precise alternative for indirect calorimetry in this population. PMID:20497783

  20. Compositional and phase relations among rare earth element minerals

    NASA Technical Reports Server (NTRS)

    Burt, D. M.

    1989-01-01

    A review is presented that mainly treats minerals in which the rare-earth elements are essential constituents, e.g., bastnaesite, monazite, xenotime, aeschynite, allanite. The chemical mechanisms and limits of REE substitution in some rock-forming minerals (zircon, apatite, titanite, garnet) are also derived. Vector representation of complex coupled substitutions in selected REE-bearing minerals is examined and some comments on REE-partitioning between minerals as related to acid-based tendencies and mineral stabilities are presented. As the same or analogous coupled substitutions involving the REE occur in a wide variety of mineral structures, they are discussed together.

  1. The rare earth element geochemistry of acid-sulphate and acid-sulphate-chloride geothermal systems from Yellowstone National Park, Wyoming, USA

    NASA Astrophysics Data System (ADS)

    Lewis, Anita J.; Palmer, Martin R.; Sturchio, Neil C.; Kemp, Anthony J.

    1997-02-01

    Rare earth element (REE) concentrations have been determined by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) in acid-sulphate and acid-sulphate-chloride waters and the associated sinters and volcanic rocks from the Yellowstone National Park (YNP), Wyoming, USA, geothermal system. REE concentrations in the volcanic rocks range from 222 to 347 ppm; their chondite-normalised REE patterns are typical of upper continental crust, with LREE > HREE and negative Eu anomalies. Total REE concentrations in the fluids range from 3 to 1133 nmol kg -1 (≥ 162 ppm), and ΣREE concentrations in sinter are ≥ 181 ppm. REE abundances and patterns in drill core material from YNP indicate some REE mobility. Normalisation of REE concentrations in altered Lava Creek Tuff (LCT) from Y-12 drill core to REE concentrations in fresh LCT indicate that the REE overall have been depleted with the exception of Eu, which has been decoupled from the REE series and concentrated in the altered rocks. Relative to the host rocks the REE patterns of the fluids are variably depleted in HREEs and LREEs, and usually have a pronounced positive Eu anomaly. This decoupling of Eu from the REE suite suggests that (1) Eu has been preferentially removed either from the host rock glass or from the host rock minerals, or (2) the waters are from a high temperature or reducing environment where Eu 2+ is more soluble than the trivalent REEs. Since the latter is inconsistent with production of acid-sulphate springs in a low temperature, oxidising near-surface environment, we suggest that the positive Eu anomalies in the fluids result from preferential dissolution of a Eu-rich phase in the host rock. Spatial and temporal variations in major element chemistry and pH of the springs sampled from Norris Geyser Basin and Crater Hills accompany variations in REE concentrations and patterns of individual geothermal springs. These are possibly related to changes in subsurface plumbing, which results in variations in

  2. Generation of abnormal trace element abundances in Antarctic eucrites by weathering processes

    NASA Technical Reports Server (NTRS)

    Mittlefehldt, David W.; Lindstrom, Marilyn M.

    1991-01-01

    Data were obtained on the trace- and major-element compositions of 16 Antarctic abnormal eucrites, many of which exhibiting positive (but sometimes negative) Ce anomalies, positive Eu anomalies, and low abundances of the remainder of the REEs. The results of data analysis suggest that the unusual REE patterns of abnormal Antarctic eucrites arise from weathering effects generated in or on the Antarctic ice. The suggested scenario involves the formation of melt water and its equilibration with the atmosphere, promoting the dissolution of REE-rich phosphates and the oxidation of Ce. As a result, tetravalent Ce is fractionated from the trivalent REE in solution.

  3. Average sedimentary rock rare Earth element patterns and crustal evolution: Some observations and implications from the 3800 Ma ISUA supracrustal belt, West Greenland

    NASA Technical Reports Server (NTRS)

    Dymek, R. F.; Boak, J. L.; Gromet, L. P.

    1983-01-01

    Rare earth element (REE) data is given on a set of clastic metasediments from the 3800 Ma Isua Supracrustal belt, West Greenland. Each of two units from the same sedimentary sequence has a distinctive REE pattern, but the average of these rocks bears a very strong resemblance to the REE pattern for the North American Shale Composite (NASC), and departs considerably from previous estimates of REE patterns in Archaean sediments. The possibility that the source area for the Isua sediments resembled that of the NASC is regarded as highly unlikely. However, REE patterns like that in the NASC may be produced by sedimentary recycling of material yielding patterns such as are found at Isua. The results lead to the following tentative conclusions: (1) The REE patterns for Isua Seq. B MBG indicate the existence of crustal materials with fractionated REE and negative Eu anomalies at 3800 Ma, (2) The average Seq. B REE pattern resembles that of the North American Shale Composite (NASC), (3) If the Seq. B average is truly representative of its crustal sources, then this early crust could have been extensively differentiated. In this regard, a proper understanding of the NASC pattern, and its relationship to post-Archaean crustal REE reservoirs, is essential, (4) The Isua results may represent a local effect.

  4. Rare earth element components in atmospheric particulates in the Bayan Obo mine region.

    PubMed

    Wang, Lingqing; Liang, Tao; Zhang, Qian; Li, Kexin

    2014-05-01

    The Bayan Obo mine, located in Inner Mongolia, China, is the largest light rare earth body ever found in the world. The research for rare earth elements (REEs) enrichment in atmospheric particulates caused by mining and ore processing is fairly limited so far. In this paper, atmospheric particulates including total suspended particulate (TSP) matter and particles with an equivalent aerodynamic diameter less than 10 μm (PM10) were collected around the Bayan Obo mine region, in August 2012 and March 2013, to analyze the levels and distributions of REEs in particles. The total concentrations of REEs for TSP were 149.8 and 239.6 ng/m(3), and those for PM10 were 42.8 and 68.9 ng/m(3), in August 2012 and March 2013, respectively. Enrichment factor was calculated for all 14 REEs in the TSP and PM10 and the results indicated that REEs enrichment in atmosphere particulates was caused by anthropogenic sources and influenced by the strong wind in springtime. The spatial distribution of REEs in TSP showed a strong gradient concentration in the prevailing wind direction. REE chondrite normalized patterns of TSP and PM10 were similar and the normalized curves inclined to the right side, showing the conspicuous fractionation between the light REEs and heavy REE, which supported by the chondrite normalized concentration ratios calculated for selected elements (La(N)/Yb(N), La(N)/Sm(N), Gd(N)/Yb(N)). PMID:24657942

  5. Bioadsorption of rare earth elements through cell surface display of lanthanide binding tags

    DOE PAGESBeta

    Park, Dan M.; Reed, David W.; Yung, Mimi C.; Eslamimanesh, Ali; Lencka, Malgorzata M.; Anderko, Andrzej; Fujita, Yoshiko; Riman, Richard E.; Navrotsky, Alexandra; Jiao, Yongqin

    2016-02-02

    In this study, with the increasing demand for rare earth elements (REEs) in many emerging clean energy technologies, there is an urgent need for the development of new approaches for efficient REE extraction and recovery. As a step toward this goal, we genetically engineered the aerobic bacterium Caulobacter crescentus for REE adsorption through high-density cell surface display of lanthanide binding tags (LBTs) on its S-layer. The LBT-displayed strains exhibited enhanced adsorption of REEs compared to cells lacking LBT, high specificity for REEs, and an adsorption preference for REEs with small atomic radii. Adsorbed Tb3+ could be effectively recovered using citrate,more » consistent with thermodynamic speciation calculations that predicted strong complexation of Tb3+ by citrate. No reduction in Tb3+ adsorption capacity was observed following citrate elution, enabling consecutive adsorption/desorption cycles. The LBT-displayed strain was effective for extracting REEs from the acid leachate of core samples collected at a prospective rare earth mine. Our collective results demonstrate a rapid, efficient, and reversible process for REE adsorption with potential industrial application for REE enrichment and separation.« less

  6. Formation of carbonatite-related giant rare-earth-element deposits by the recycling of marine sediments.

    PubMed

    Hou, Zengqian; Liu, Yan; Tian, Shihong; Yang, Zhiming; Xie, Yuling

    2015-01-01

    Carbonatite-associated rare-earth-element (REE) deposits are the most significant source of the world's REEs; however, their genesis remains unclear. Here, we present new Sr-Nd-Pb and C-O isotopic data for Cenozoic carbonatite-hosted giant REE deposits in southwest China. These REE deposits are located along the western margin of the Yangtze Craton that experienced Proterozoic lithospheric accretion, and controlled by Cenozoic strike-slip faults related to Indo-Asian continental collision. The Cenozoic carbonatites were emplaced as stocks or dykes with associated syenites, and tend to be extremely enriched in Ba, Sr, and REEs and have high (87)Sr/(86)Sr ratios (>0.7055). These carbonatites were likely formed by melting of the sub-continental lithospheric mantle (SCLM), which had been previously metasomatized by high-flux REE- and CO2-rich fluids derived from subducted marine sediments. The fertility of these carbonatites depends on the release of REEs from recycled marine sediments and on the intensity of metasomatic REE refertilization of the SCLM. We suggest that cratonic edges, particularly along ancient convergent margins, possess the optimal configuration for generating giant REE deposits; therefore, areas of metamorphic basement bounded or cut by translithospheric faults along cratonic edges have a high potential for such deposits. PMID:26035414

  7. Pilot Study to Explore the Accuracy of Current Prediction Equations in Assessing Energy Needs of Patients with Newly Diagnosed Glioblastoma Multiforme.

    PubMed

    Little, Rebecca B; Oster, Robert A; Darnell, Betty E; Demark-Wahnefried, Wendy; Nabors, L Burt

    2016-01-01

    Glioblastoma multiforme (GBM) is rare, yet it is the most common brain malignancy and has a poor prognosis. In regard to GBM, there is a dearth of research on resting energy expenditure (REE) and the accuracy of extant prediction equations. The aim of this cross-sectional study was to compare measured REE (mREE) to commonly used prediction equations in newly diagnosed GBM patients. REE was collected by indirect calorimetry in 20 GBM patients. Calculated REE was derived from Harris-Benedict (again with weight adjusted for obesity), Mifflin-St Jeor, and the 20 kcal/kg body weight ratio method. Paired t-tests and Bland-Altman analyses were used to compare group means, evaluate the bias, and find the limits of agreement. Clinical accuracy was assessed by determining the percentage of patients with predicted REE within ±10% of mREE. Subjects were evenly distributed with regard to gender, primarily Caucasian, and largely overweight or obese and had a mean age of 57 years. All equations overestimated mREE. Mifflin-St Jeor and adjusted Harris-Benedict had the narrowest limits of agreement and accurately predicted 60% and 65% of subjects, respectively. Clinicians should be aware of the discrepancy between commonly used prediction equations and REE. More research is needed to verify these findings and decipher the cause and significance in the GBM population. PMID:27341142

  8. Rare earth element distribution in >400 °C hot hydrothermal fluids from 5°S, MAR: The role of anhydrite in controlling highly variable distribution patterns

    NASA Astrophysics Data System (ADS)

    Schmidt, K.; Garbe-Schönberg, D.; Bau, M.; Koschinsky, A.

    2010-07-01

    Two submarine hydrothermal vent fields at 5°S, Mid-Atlantic Ridge (MAR) - Turtle Pits and Comfortless Cove - emanate vapor-phase fluids at conditions close to the critical point of seawater (407 °C, 298 bars). In this study, the concentration and distribution of rare earth element (REE) and yttrium (Y) has been investigated. Independent of the major element composition, the fluids display a strong temporal variability of their REE + Y concentrations and relative distributions at different time scales of minutes to years. Chondrite-normalized distributions range from common fluid patterns with light REE enrichment relative to the heavy REE, accompanied by positive Eu anomalies (type I), to strongly REE + Y enriched patterns with a concave-downward distribution with a maximum enrichment of Sm and weakly positive or even negative Eu anomalies (type II). The larger the sum of REE, the smaller Ce CN/Yb CN and Eu/Eu∗. We also observed a strong variability in fluid flow and changing fluid temperatures, correlating with the compositional variability. As evident by the positive correlation of total REE, Ca, and Sr concentrations in Turtle Pits and Comfortless Cove fluids, precipitation/dissolution of hydrothermal anhydrite controls the variability in REE concentrations and distributions in these fluids and the transformation of one fluid type to the other. The variable distribution of REE can be explained by the accumulation of particulate anhydrite (with concave-downward REE distribution and negative Eu anomaly) into a fluid with common REE distribution (type I), followed by the modification of the REE fluid signature due to dissolution of incorporated anhydrite. A second model, in which the type II fluids represent a primary REE reaction zone fluid pattern, which is variably modified by precipitation of anhydrite, can also explain the observed correlations of total REE, fractionation of LREE/HREE and size of Eu anomaly as well as Ca, Sr. The emanation of such a fluid

  9. Importance of vertical geochemical processes in controlling the oceanic profiles of dissolved rare earth elements in the northeastern Indian Ocean

    NASA Astrophysics Data System (ADS)

    Nozaki, Yoshiyuki; Alibo, Dia Sotto

    2003-01-01

    Vertical profiles of dissolved rare earth elements (REEs) were obtained in the Bay of Bengal and the Andaman Sea. The REE concentrations at various depths in the Bay of Bengal are the highest in the Indian Ocean. This is attributable ultimately to the large outflow of the Ganges-Brahmaputra and Irrawaddy rivers, but the dissolved REE flux to surface waters alone cannot explain the large and near-constant REE enrichment throughout the entire water column. The underlying fan sediments serve as not a source but a sink for dissolved REE(III)s. Absence of excess 228Ra in the deep waters suggests that lateral input of dissolved REEs from slope sediments is also small in these regions. Partial (<0.3%) dissolution of detrital particles, which are carried by the rivers and lateral surface currents and subsequently settle through the water column, appears to be a predominant source for the dissolved REEs. Vertical profiles showing an almost linear increase with depth are common features for the light and middle REEs everywhere, but their concentration levels are variable from basin to basin and from element to element. This suggests that their oceanic distributions respond quickly to the variation of particle flux and its REE composition through reversible exchange equilibrium with suspended and sinking particles much like the case for Th. The relative importance of the vertical geochemical processes of reversible scavenging over the horizontal basin-scale ocean circulation with passive regeneration like nutrients decreases systematically from the light to the heavy REEs. Using a model, the mean oceanic residence times of REEs in the Bay of Bengal are estimated to range from 37 years for Ce to 140-1510 years for the strictly trivalent REEs. In the deep water of the Andaman Sea, isolated from the Bay of Bengal by the Andaman-Nicobar Ridge (maximum sill depth of ˜1800 m), the REE concentrations are almost uniform presumably due to rapid vertical mixing. The REE

  10. Rare earth element geochemistry of massive sulfides-sulfates and gossans on the Southern Explorer Ridge

    SciTech Connect

    Barrett, T.J. ); Jarvis, I. ); Jarvis, K.E. )

    1990-07-01

    Massive sulfide-sulfate deposits on the Southern Explorer Ridge were analyzed for 14 rare earth elements (REE) by a modified inductively coupled plasma-mass spectrometric technique that included a correction for high Ba content. Bulk samples of finely intermixed sulfides, sulfate, and amorphous silica contain {Sigma}REE concentrations of {le} 6 ppm. REE patterns range from (1) strongly enriched in light REE with positive Eu anomalies, to (2) relatively flat with positive Eu anomalies and slightly negative Ce anomalies, to (3) slightly enriched in light REE with moderately negative Ce anomalies. Pattern 1 is similar to that of 300-350 C solutions discharging at vents on the East Pacific Rise and the Mid-Atlantic Ridge, whereas pattern 3 resembles REE distributions in normal oceanic bottom waters. The sulfide-sulfate patterns are interpreted to result from variable mixtures of hydrothermal and normal seawater. Barite in gossans capping the mounds has an REE pattern almost identical to patterns of high-temperature vent solutions. Hydrothermal barite has lower REE contents and a different REE pattern relative to hydrogenous barite formed slowly on the sea floor.

  11. Bioadsorption of Rare Earth Elements through Cell Surface Display of Lanthanide Binding Tags.

    PubMed

    Park, Dan M; Reed, David W; Yung, Mimi C; Eslamimanesh, Ali; Lencka, Malgorzata M; Anderko, Andrzej; Fujita, Yoshiko; Riman, Richard E; Navrotsky, Alexandra; Jiao, Yongqin

    2016-03-01

    With the increasing demand for rare earth elements (REEs) in many emerging clean energy technologies, there is an urgent need for the development of new approaches for efficient REE extraction and recovery. As a step toward this goal, we genetically engineered the aerobic bacterium Caulobacter crescentus for REE adsorption through high-density cell surface display of lanthanide binding tags (LBTs) on its S-layer. The LBT-displayed strains exhibited enhanced adsorption of REEs compared to cells lacking LBT, high specificity for REEs, and an adsorption preference for REEs with small atomic radii. Adsorbed Tb(3+) could be effectively recovered using citrate, consistent with thermodynamic speciation calculations that predicted strong complexation of Tb(3+) by citrate. No reduction in Tb(3+) adsorption capacity was observed following citrate elution, enabling consecutive adsorption/desorption cycles. The LBT-displayed strain was effective for extracting REEs from the acid leachate of core samples collected at a prospective rare earth mine. Our collective results demonstrate a rapid, efficient, and reversible process for REE adsorption with potential industrial application for REE enrichment and separation. PMID:26836847

  12. Formation of carbonatite-related giant rare-earth-element deposits by the recycling of marine sediments

    PubMed Central

    Hou, Zengqian; Liu, Yan; Tian, Shihong; Yang, Zhiming; Xie, Yuling

    2015-01-01

    Carbonatite-associated rare-earth-element (REE) deposits are the most significant source of the world’s REEs; however, their genesis remains unclear. Here, we present new Sr-Nd-Pb and C-O isotopic data for Cenozoic carbonatite-hosted giant REE deposits in southwest China. These REE deposits are located along the western margin of the Yangtze Craton that experienced Proterozoic lithospheric accretion, and controlled by Cenozoic strike-slip faults related to Indo-Asian continental collision. The Cenozoic carbonatites were emplaced as stocks or dykes with associated syenites, and tend to be extremely enriched in Ba, Sr, and REEs and have high 87Sr/86Sr ratios (>0.7055). These carbonatites were likely formed by melting of the sub-continental lithospheric mantle (SCLM), which had been previously metasomatized by high-flux REE- and CO2-rich fluids derived from subducted marine sediments. The fertility of these carbonatites depends on the release of REEs from recycled marine sediments and on the intensity of metasomatic REE refertilization of the SCLM. We suggest that cratonic edges, particularly along ancient convergent margins, possess the optimal configuration for generating giant REE deposits; therefore, areas of metamorphic basement bounded or cut by translithospheric faults along cratonic edges have a high potential for such deposits. PMID:26035414

  13. Diel behavior of rare earth elements in a mountain stream with acidic to neutral pH

    USGS Publications Warehouse

    Gammons, C.H.; Wood, S.A.; Nimick, D.A.

    2005-01-01

    Diel (24-h) changes in concentrations of rare earth elements (REE) were investigated in Fisher Creek, a mountain stream in Montana that receives acid mine drainage in its headwaters. Three simultaneous 24-h samplings were conducted at an upstream station (pH = 3.3), an intermediate station (pH = 5.5), and a downstream station (pH = 6.8). The REE were found to behave conservatively at the two upstream stations. At the downstream station, REE partitioned into suspended particles to a degree that varied with the time of day, and concentrations of dissolved REE were 2.9- to 9.4-fold (190% to 830%) higher in the early morning vs. the late afternoon. The decrease in dissolved REE concentrations during the day coincided with a corresponding increase in the concentration of REE in suspended particles, such that diel changes in the total REE concentrations were relatively minor (27% to 55% increase at night). Across the lanthanide series, the heavy REE partitioned into the suspended solid phase to a greater extent than the light REE. Filtered samples from the downstream station showed a decrease in shale-normalized REE concentration across the lanthanide series, with positive anomalies at La and Gd, and a negative Eu anomaly. As the temperature of the creek increased in the afternoon, the slope of the REE profile steepened and the magnitude of the anomalies increased. The above observations are explained by cyclic adsorption of REE onto suspended particles of hydrous ferric and aluminum oxides (HFO, HAO). Conditional partition coefficients for each REE between the suspended solids and the aqueous phase reached a maximum at 1700 hours and a minimum at 0700 hours. This pattern is attributed to diel variations in stream temperature, possibly reinforced by kinetic factors (i.e., slower rates of reaction at night than during the day). Estimates of the enthalpy of adsorption of each REE onto suspended particles based on the field results averaged +82 kJ/mol and are similar in

  14. Early depositional history of metalliferous sediments in the Atlantis II Deep of the Red Sea: Evidence from rare earth element geochemistry

    NASA Astrophysics Data System (ADS)

    Laurila, Tea E.; Hannington, Mark D.; Petersen, Sven; Garbe-Schönberg, Dieter

    2014-02-01

    The Atlantis II Deep is a brine-filled depression on the slowly spreading Red Sea rift axis. It is by far the largest deposit of hydrothermally precipitated metals on the present ocean floor and the only known modern deposit that is analogous to laminated Fe-rich chemical sediments, such as banded iron formation (BIF). The brine pool at the bottom of the Atlantis II Deep creates an environment where most of the hydrothermally sourced elements can be dispersed and deposited over an area of ˜60 km2. We analyzed the rare earth element concentrations in 100 small-volume samples from 9 cores in different parts of the Atlantis II Deep to better understand the origins of different types of metalliferous sediments (detrital, proximal hydrothermal and distal hydrothermal). Our results agree with earlier studies based on larger bulk samples that show the composition of the major depositional units is related to major changes in the location and intensity of hydrothermal activity and the amount of hydrothermal versus background sedimentation. In this paper, we address the origins of chemically distinct laminae (down to sub-millimeter) that correspond to ˜annual deposition. REE patterns clearly reflect 3 different sources (e.g., detrital, scavenging, direct hydrothermal input). Detrital REE that are delivered to the Deep from outside account for most of the REE in the sediments of the Atlantis II Deep, similar to BIF, and are unaffected by fractionation due to hydrothermal processes during deposition and diagenesis. Fe- and Mn-(oxy)hydroxides that form at the anoxic-oxic boundary scavenge REE from the brine pool as they settle. The Fe-(oxy)hydroxides contain a larger proportion of REE from seawater than any other sediment-type and also scavenge REE from pore waters after deposition. In contrast, the Mn-(oxy)hydroxides dissolve before deposition and thus function as transporting agents between seawater and the brine. However, there is little evidence for direct seawater

  15. Diel behavior of rare earth elements in a mountain stream with acidic to neutral pH

    NASA Astrophysics Data System (ADS)

    Gammons, Christopher H.; Wood, Scott A.; Nimick, David A.

    2005-08-01

    Diel (24-h) changes in concentrations of rare earth elements (REE) were investigated in Fisher Creek, a mountain stream in Montana that receives acid mine drainage in its headwaters. Three simultaneous 24-h samplings were conducted at an upstream station (pH = 3.3), an intermediate station (pH = 5.5), and a downstream station (pH = 6.8). The REE were found to behave conservatively at the two upstream stations. At the downstream station, REE partitioned into suspended particles to a degree that varied with the time of day, and concentrations of dissolved REE were 2.9- to 9.4-fold (190% to 830%) higher in the early morning vs. the late afternoon. The decrease in dissolved REE concentrations during the day coincided with a corresponding increase in the concentration of REE in suspended particles, such that diel changes in the total REE concentrations were relatively minor (27% to 55% increase at night). Across the lanthanide series, the heavy REE partitioned into the suspended solid phase to a greater extent than the light REE. Filtered samples from the downstream station showed a decrease in shale-normalized REE concentration across the lanthanide series, with positive anomalies at La and Gd, and a negative Eu anomaly. As the temperature of the creek increased in the afternoon, the slope of the REE profile steepened and the magnitude of the anomalies increased. The above observations are explained by cyclic adsorption of REE onto suspended particles of hydrous ferric and aluminum oxides (HFO, HAO). Conditional partition coefficients for each REE between the suspended solids and the aqueous phase reached a maximum at 1700 hours and a minimum at 0700 hours. This pattern is attributed to diel variations in stream temperature, possibly reinforced by kinetic factors (i.e., slower rates of reaction at night than during the day). Estimates of the enthalpy of adsorption of each REE onto suspended particles based on the field results averaged +82 kJ/mol and are similar in

  16. LA-ICP-MS analysis of isolated phosphatic grains indicates selective rare earth element enrichment during reworking and transport processes

    NASA Astrophysics Data System (ADS)

    Auer, Gerald; Reuter, Markus; Hauzenberger, Christoph A.; Piller, Werner E.

    2016-04-01

    Rare earth elements (REE) are a commonly used proxy to reconstruct water chemistry and oxygen saturation during the formation history of authigenic and biogenic phosphates in marine environments. In the modern ocean REE exhibit a distinct pattern with enrichment of heavy REE and strong depletion in Cerium. Studies of ancient phosphates and carbonates, however, showed that this 'modern' pattern is only rarely present in the geological past. Consequently, the wide range of REE enrichment patterns found in ancient marine phosphates lead to the proposition that water chemistry had to have been radically different in the earth's past. A wealth of studies has already shown that both early and late diagenesis can strongly affect REE signatures in phosphates and severely alter primary marine signals. However, no previous research was conducted on how alteration processes occurring prior to final deposition affect marine phosphates. Herein we present a dataset of multiple LA-ICP-MS measurements of REE signatures in isolated phosphate and carbonate grains deposited in a carbonate ramp setting in the central Mediterranean Sea during the middle Miocene "Monterey event". The phosphates are represented by authigenic, biogenic and detrital grains emplaced in bioclastic grain- to packstones dominated by bryozoan and echinoderm fragments, as well as abundant benthic and planktic foraminifers. The results of 39 grain specific LA-ICP-MS measurements in three discrete rock samples reveals four markedly different REE patterns (normalized to the Post Archean Australian Shale standard) in terms of total enrichment and pattern shape. Analyses of REE diagenesis proxies show that diagenetic alteration affected the samples only to a minor degree. Considering grain shape and REE patterns together indicate that authigenic, detrital and biogenic phosphates have distinct REE patterns irrespective of the sample. Our results show that the observed REE patterns in phosphates only broadly reflect

  17. Investigating Rare Earth Element Systematics in the Marcellus Shale

    NASA Astrophysics Data System (ADS)

    Yang, J.; Torres, M. E.; Kim, J. H.; Verba, C.

    2014-12-01

    The lanthanide series of elements (the 14 rare earth elements, REEs) have similar chemical properties and respond to different chemical and physical processes in the natural environment by developing unique patterns in their concentration distribution when normalized to an average shale REE content. The interpretation of the REE content in a gas-bearing black shale deposited in a marine environment must therefore take into account the paleoredox conditions of deposition as well as any diagenetic remobilization and authigenic mineral formation. We analyzed 15 samples from a core of the Marcellus Shale (Whipkey ST1, Greene Co., PA) for REEs, TOC, gas-producing potential, trace metal content, and carbon isotopes of organic matter in order to determine the REE systematics of a black shale currently undergoing shale gas development. We also conducted a series of sequential leaching experiments targeting the phosphatic fractions in order to evaluate the dominant host phase of REEs in a black shale. Knowledge of the REE system in the Marcellus black shale will allow us to evaluate potential REE release and behavior during hydraulic fracturing operations. Total REE content of the Whipkey ST1 core ranged from 65-185 μg/g and we observed three distinct REE shale-normalized patterns: middle-REE enrichment (MREE/MREE* ~2) with heavy-REE enrichment (HREE/LREE ~1.8-2), flat patterns, and a linear enrichment towards the heavy-REE (HREE/LREE ~1.5-2.5). The MREE enrichment occurred in the high carbonate samples of the Stafford Member overlying the Marcellus Formation. The HREE enrichment occurred in the Union Springs Member of the Marcellus Formation, corresponding to a high TOC peak (TOC ~4.6-6.2 wt%) and moderate carbonate levels (CaCO3 ~4-53 wt%). Results from the sequential leaching experiments suggest that the dominant host of the REEs is the organic fraction of the black shale and that the detrital and authigenic fractions have characteristic MREE enrichments. We present our

  18. Attenuation of rare earth elements in a boreal estuary

    NASA Astrophysics Data System (ADS)

    Åström, Mats E.; Österholm, Peter; Gustafsson, Jon Petter; Nystrand, Miriam; Peltola, Pasi; Nordmyr, Linda; Boman, Anton

    2012-11-01

    This study focuses on attenuation of rare earth elements (REE) when a boreal creek, acidified and loaded with REE and other metals as a result of wetland drainage, empties into a brackish-water estuary (salinity < 6‰). Surface water was collected in a transect from the creek mouth to the outer estuary, and settling (particulate) material in sediment traps moored at selected locations in the estuary. Ultrafiltration, high-resolution ICP-MS and modeling were applied on the waters, and a variety of chemical reagents were used to extract metals from the settling material. Aluminium, Fe and REE transported by the acidic creek were extensively removed in the inner/central estuary where the acidic water was neutralised, whereas Mn was relatively persistent in solution and thus redistributed to particles and deposited further down the estuary. The REE removal was caused by several contemporary mechanisms: co-precipitation with oxyhydroxides (mainly Al but also Fe), complexation with flocculating humic substances and sorption to suspended particles. Down estuary the dissolved REE pool, remaining after removal, was fractionated: the <1 kDa pool became depleted in the middle REE and the colloidal (0.45 μm-1 kDa) pool depleted in the middle and heavy REE. This fractionation was controlled by the removal process, such that those REE with highest affinity for the settling particles became most depleted in the remaining dissolved pool. Modeling, based on Visual MINTEQ version 3.0 and the Stockholm Humic Model after revision and updating, predicted that the dissolved (<0.45 μm) REE pool in the estuary is bound almost entirely to humic substances. Acid sulphate soils, the source of the REE and other metals in the creek water, are widespread on coastal plains worldwide and therefore the REE attenuation patterns and mechanisms identified in the studied estuary are relevant for recognition of similar geochemical processes and conditions in a variety of coastal locations.

  19. Rare earth elements in the phosphatic-enriched sediment of the Peru shelf

    USGS Publications Warehouse

    Piper, D.Z.; Baedecker, P.A.; Crock, J.G.; Burnett, W.C.; Loebner, B.J.

    1988-01-01

    Apatite-enriched materials from the Peru shelf have been analyzed for their major oxide and rare earth element (REE) concentrations. The samples consist of (1) the fine fraction of sediment, mostly clay material, (2) phosphatic pellets and fish debris, which are dispersed throughout the fine-grained sediment, (3) tabular-shaped phosphatic crusts, which occur within the uppermost few centimeters of sediment, and (4) phosphatic nodules, which occur on the seafloor. The bulk REE concentrations of the concretions suggest that these elements are partitioned between the enclosed detrital material and the apatite fraction. Analysis of the fine-grained sediment with which the samples are associated suggested that this detrital fraction in the concretions should have shale REE values; the analysis of the fish debris suggested that the apatite fraction might have seawater values. The seawater contribution of REE's is negligible in the nodules and crust, in which the apatite occurs as a fine-grained interstitial cement. That is, the concentration of REE's and the REE patterns are predominantly a function of the amount of enclosed fine-grained sediment. By contrast, the REE pattern of the pelletal apatite suggests a seawater source and the absolute REE concentrations are relatively high. The REE P2O5 ratios of the apatite fraction of these samples thus vary from approximately zero (in the case of the crust and nodules) to as much as approximately 1.2 ?? 10-3 (in the case of the pellets). The range of this ratio suggests that rather subtle variations in the depositional environment might cause a significant variation in the REE content of this authigenic fraction of the sediment. Pelletal glauconite was also recovered from one sediment core. Its REE concentrations closely resemble those of the fish debris. ?? 1988.

  20. Rare earth element geochemistry in cold-seep pore waters of Hydrate Ridge, northeast Pacific Ocean

    NASA Astrophysics Data System (ADS)

    Himmler, Tobias; Haley, Brian A.; Torres, Marta E.; Klinkhammer, Gary P.; Bohrmann, Gerhard; Peckmann, Jörn

    2013-07-01

    The concentrations of rare earth elements (REEs), sulphate, hydrogen sulphide, total alkalinity, calcium, magnesium and phosphate were measured in shallow (<12 cm below seafloor) pore waters from cold-seep sediments on the northern and southern summits of Hydrate Ridge, offshore Oregon. Downward-decreasing sulphate and coevally increasing sulphide concentrations reveal sulphate reduction as dominant early diagenetic process from ~2 cm depth downwards. A strong increase of total dissolved REE (∑REE) concentrations is evident immediately below the sediment-water interface, which can be related to early diagenetic release of REEs into pore water resulting from the re-mineralization of particulate organic matter. The highest pore water ∑REE concentrations were measured close to the sediment-water interface at ~2 cm depth. Distinct shale-normalized REE patterns point to particulate organic matter and iron oxides as main REE sources in the upper ~2-cm depth interval. In general, the pore waters have shale-normalized patterns reflecting heavy REE (HREE) enrichment, which suggests preferential complexation of HREEs with carbonate ions. Below ~2 cm depth, a downward decrease in ∑REE correlates with a decrease in pore water calcium concentrations. At this depth, the anaerobic oxidation of methane (AOM) coupled to sulphate reduction increases carbonate alkalinity through the production of bicarbonate, which results in the precipitation of carbonate minerals. It seems therefore likely that the REEs and calcium are consumed during vast AOM-induced precipitation of carbonate in shallow Hydrate Ridge sediments. The analysis of pore waters from Hydrate Ridge shed new light on early diagenetic processes at cold seeps, corroborating the great potential of REEs to identify geochemical processes and to constrain environmental conditions.

  1. Effect of paracentesis on metabolic activity in patients with advanced cirrhosis and ascites.

    PubMed

    Knudsen, Anne Wilkens; Krag, Aleksander; Nordgaard-Lassen, Inge; Frandsen, Erik; Tofteng, Flemming; Mortensen, Christian; Becker, Ulrik

    2016-05-01

    Objective Patients with decompensated cirrhosis often suffer from malnutrition. To enable appropriate nutritional supplementation a correct estimation of resting energy expenditure (REE) is needed. It is, however, unclear whether the volume of ascites should be included or not in the calculations of the REE. Material and methods In 19 patients with cirrhosis and ascites, measurements of REE by indirect calorimetry were performed before paracentesis, after paracentesis, and four weeks after paracentesis. Moreover, handgrip strength (HGS), dual X-ray absorptiometry (DXA), and biochemistry were assessed. Results Calculated and measured REE differed more than 10% in 63% of the patients at baseline. By including the weight of ascites in the calculation of REE, the REE was overestimated by 283 (-602-1381) kJ/day (p = 0.69). By subtracting the weight of ascites in the calculation of REE, it was underestimated by -379 (-1915 - 219) kJ/day, (p  = 0.06). Patients in whom measured REE decreased after paracentesis had higher middle arterial pressure (MAP) (p = 0.02) and p-sodium (p = 0.02) at baseline. Low HGS (M: <30 kg; W < 20 kg) was evident in 68% of the patients. T-scores revealed osteopenia and osteoporosis in 58% and 16%, respectively. Reduced vitamin D levels (<50 nmol/l) were found in 68%. Conclusions The presence of ascites seems to increase REE, why we suggest that when REE is calculated, the weight of ascites should be included. Indirect calorimetry is, however, preferable for REE estimation. More than two-third of patients with ascites suffer from muscle weakness and/or osteopenia. PMID:26673350

  2. Rare earth element geochemistry of outcrop and core samples from the Marcellus Shale

    SciTech Connect

    Noack, Clinton W.; Jain, Jinesh C.; Stegmeier, John; Hakala, J. Alexandra; Karamalidis, Athanasios K.

    2015-06-26

    In this paper, we studied the geochemistry of the rare earth elements (REE) in eleven outcrop samples and six, depth-interval samples of a core from the Marcellus Shale. The REE are classically applied analytes for investigating depositional environments and inferring geochemical processes, making them of interest as potential, naturally occurring indicators of fluid sources as well as indicators of geochemical processes in solid waste disposal. However, little is known of the REE occurrence in the Marcellus Shale or its produced waters, and this study represents one of the first, thorough characterizations of the REE in the Marcellus Shale. In these samples, the abundance of REE and the fractionation of REE profiles were correlated with different mineral components of the shale. Namely, samples with a larger clay component were inferred to have higher absolute concentrations of REE but have less distinctive patterns. Conversely, samples with larger carbonate fractions exhibited a greater degree of fractionation, albeit with lower total abundance. Further study is necessary to determine release mechanisms, as well as REE fate-and-transport, however these results have implications for future brine and solid waste management applications.

  3. Tracing sediment movement on semi-arid watershed using Rare Earth Elements 1988

    Technology Transfer Automated Retrieval System (TEKTRAN)

    A multi-tracer method employing rare earth elements (REE) was used to determine sediment yield and to track sediment movement in a small semiarid watershed. A 0.33 ha watershed near Tombstone, AZ was divided into five morphological units, each tagged with one of five REE oxides. Relative contributi...

  4. 76 FR 4408 - 60-Day Notice of Proposed Information Collection: Form DS-1998E, Foreign Service Officer Test...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-01-25

    ... State is seeking Office of Management and Budget (OMB) approval for the information collection described... Office: Human Resources, HR/REE/BEX. Form Number: DS-1998E. Respondents: Registrants for the Foreign... Rosenberry, HR/REE/ BEX, SA-44, 301 4th St., SW., Room 324, Washington, DC 20547. Fax: (202) 923-6472....

  5. Rare-earth elements distribution in granulite-facies marbles: a witness of fluid rock interaction

    NASA Astrophysics Data System (ADS)

    Boulvais, Philippe; Fourcade, Serge; Moine, Bernard; Gruau, Gérard; Cuney, Michel

    2000-08-01

    The rare earth element (REE) distribution of marbles from Tranomaro (SE Madagascar) shows that the marbles have interacted with syn-metamorphic fluids during the Panafrican granulite-facies metamorphism. The Tranomaro area is characterized by an extensive development of pyroxenites (skarns) variably mineralized in uranothorianite and enriched in REE, Zr. Across a meter-scale marble-pyroxenite contact, the REE content increases from the most remote marble sample to the contact with the pyroxenite (La from 19.8 to 129 ppm). REE patterns in enriched marbles display a strong negative Eu anomaly similar to those of pyroxenites. This peculiar type of REE distribution results from fluid infiltration. On a regional scale, some marbles have similar REE characteristics (progressive development of Eu anomaly together with REE enrichment) showing that some of them have interacted with fluids. Infiltration was hardly recognizable using C and O isotopic signatures because large isotopic variations were introduced during the pre-granulitic history. Then, REE distribution in high-grade marble may be helpful in monitoring syn-metamorphic fluid flow. In the present case, it is a more reliable tracer of fluid infiltration than stable isotopic compositions.

  6. Selective europium and cerium phases in the regolith of mare crisium

    NASA Astrophysics Data System (ADS)

    Mokhov, A. V.; Gornostaeva, T. A.; Kartashov, P. M.; Bogatikov, O. A.

    2015-11-01

    Two particles selectively enriched in REEs (one in Eu, the other in Ce) were found during the study of samples of the lunar regolith delivered to the Earth by AS Luna-24. They may be related to oxides or carbides. Thus, the fact of the presence of specific processes resulting in deep REE differentiation on the Moon is supported.

  7. Effects of White Radish (Raphanus sativus) Enzyme Extract on Hepatotoxicity.

    PubMed

    Lee, Sang Wha; Yang, Kwang Mo; Kim, Jung Ki; Nam, Byung Hyouk; Lee, Chang Min; Jeong, Min Ho; Seo, Su Yeong; Kim, Gi Yong; Jo, Wol-Soon

    2012-09-01

    Raphanus sativus (Cruciferaceae), commonly known as radish is widely available throughout the world. From antiquity it has been used in folk medicine as a natural drug against many toxicants. The present study was designed to evaluate the hepatoprotective activity of radish (Raphanus sativus) enzyme extract (REE) in vitro and in vivo test. The IC50 values of REE in human liver derived HepG2 cells was over 5,000 μg/ml in tested maximum concentration. The effect of REE to protect tacrine-induced cytotoxicity in HepG2 cells was evaluated by MTT assay. REE showed their hepatoprotective activities on tacrineinduced cytotoxicity and the EC50 value was 1,250 μg/ml. Silymarin, an antihepatotoxic agent used as a positive control exhibited 59.7% hepatoprotective activitiy at 100 μg/ml. Moreover, we tested the effect of REE on carbon tetrachloride (CCl4)-induced liver toxicity in rats. REE at dose of 50 and 100 mg/kg and silymarin at dose of 50 mg/kg were orally administered to CCl4-treated rats. The results showed that REE and silymarin significantly reduced the elevated levels of serum enzyme markers induced by CCl4. The biochemical data were supported by evaluation with liver histopathology. These findings suggest that REE, can significantly diminish hepatic damage by toxic agent such as tacrine or CCl4. PMID:24278606

  8. Rare earth element geochemistry of outcrop and core samples from the Marcellus Shale

    DOE PAGESBeta

    Noack, Clinton W.; Jain, Jinesh C.; Stegmeier, John; Hakala, J. Alexandra; Karamalidis, Athanasios K.

    2015-06-26

    In this paper, we studied the geochemistry of the rare earth elements (REE) in eleven outcrop samples and six, depth-interval samples of a core from the Marcellus Shale. The REE are classically applied analytes for investigating depositional environments and inferring geochemical processes, making them of interest as potential, naturally occurring indicators of fluid sources as well as indicators of geochemical processes in solid waste disposal. However, little is known of the REE occurrence in the Marcellus Shale or its produced waters, and this study represents one of the first, thorough characterizations of the REE in the Marcellus Shale. In thesemore » samples, the abundance of REE and the fractionation of REE profiles were correlated with different mineral components of the shale. Namely, samples with a larger clay component were inferred to have higher absolute concentrations of REE but have less distinctive patterns. Conversely, samples with larger carbonate fractions exhibited a greater degree of fractionation, albeit with lower total abundance. Further study is necessary to determine release mechanisms, as well as REE fate-and-transport, however these results have implications for future brine and solid waste management applications.« less

  9. Interactions between exogenous rare earth elements and phosphorus leaching in packed soil columns

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Rare earth elements (REEs) increasingly used in agriculture as an amendment for crop growth may help to lessen environmental losses of phosphorus (P) from heavily fertilized soils. The vertical transport characteristics of P and REEs, lanthanum (La), neodymium (Nd), samarium (Sm), and cerium (Ce), w...

  10. 7 CFR 550.16 - Project development.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 7 Agriculture 6 2010-01-01 2010-01-01 false Project development. 550.16 Section 550.16 Agriculture... § 550.16 Project development. REE provides partial funding to Cooperators to support research projects... the REE Agency's ADODR shall jointly develop the following documentation: (a) Project plan. A...

  11. Shaker Table Experiments with Rare Earth Elements Sorption from Geothermal Brine

    SciTech Connect

    Gary Garland

    2015-07-21

    This dataset described shaker table experiments ran with sieved -50 +100 mesh media #1 in brine #1 that have 2ppm each of the 7 REE metals at different starting pH's of 3.5, 4.5, and 5.5. The experimental conditions are 2g media to 150mL of REE solution, at 70C.

  12. Levels of rare earth elements, heavy metals and uranium in a population living in Baiyun Obo, Inner Mongolia, China: a pilot study.

    PubMed

    Hao, Zhe; Li, Yonghua; Li, Hairong; Wei, Binggan; Liao, Xiaoyong; Liang, Tao; Yu, Jiangping

    2015-06-01

    The Baiyun Obo deposit is the world's largest rare earth elements (REE) deposit. We aimed to investigate levels of REE, heavy metals (HMs) and uranium (U) based on morning urine samples in a population in Baiyun Obo and to assess the possible influence of rare earth mining processes on human exposure. In the mining area, elevated levels were found for the sum of the concentrations of light REE (LREE) and heavy REE (HREE) with mean values at 3.453 and 1.151 μg g(-1) creatinine, which were significantly higher than those in the control area. Concentrations of HMs and U in the population increased concomitantly with increasing REE levels. The results revealed that besides REE, HMs and U were produced with REE exploitation. Gender, age, educational level, alcohol and smoking habit were major factors contributing to inter-individual variation. Males were more exposed to these metals than females. Concentrations in people in the senior age group and those with only primary education were low. Drinking and smoking were associated with the levels of LREE, Cr, Cu, Cd and Pb in morning urine. Hence this study provides basic and useful information when addressing public and environmental health challenges in the areas where REE are mined and processed. PMID:25703899

  13. 76 FR 10755 - Establishment of Office of the Chief Scientist; Revision of Delegations of Authority

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-02-28

    ... establishment of the Office of the Chief Scientist within the Research, Education, and Economics (REE) mission...) established the Office of the Chief Scientist (OCS) within the Research, Education, and Economics (REE... animal products; agricultural systems and technology; and agricultural economics and rural...

  14. The Efficacy of Rational Emotive Education for Acting-Out and Socially Withdrawn Adolescents.

    ERIC Educational Resources Information Center

    Voelm, Clint E.; And Others

    Rational Emotive Education (REE), derived from Rational Emotive Therapy (RET), is a humanistic approach for helping children cope more objectively and effectively with the stress of modern living and personal problems. To investigate the efficacy of teaching REE, 38 acting-out and 42 socially withdrawn adolescents were randomly assigned to one of…

  15. Geochemistry of organic-rich black shales overlying the natural nuclear fission reactors of Oklo, Republic of Gabon

    SciTech Connect

    Mossman, D.J.; Gauthier-Lafaye, F.; Nagy, B.; Rigali, M.J.

    1998-07-01

    The organic-rich black shales of the Franceville Series` FB Formation overlying the uranium ores, and natural nuclear fission reactors of Oklo, Gabon, are not notably metalliferous. Chromium, gold, silver, and barium are slightly enriched in average Oklo black shale (AOK) relative to black shale standard SDO-1. Geochemical variations among the black shale samples of the sedimentary sequence include enrichment in potassium, barium, chromium, and silver in the four lowermost samples, the presence of a bleached zone depleted in organic carbon lowermost in the sequence, and elevated rare earth element (REE) content in samples closest to the Oklo reactor zones. Hydrothermal activity has influenced the geochemistry of the black shale but is evidently not linked to reactor-driven processes. Chondrite-normalized REE patterns of Oklo black shale samples show slight enrichment in light REE and slight depletion in heavy REE, especially in the sample closest to the reactor zone. However, comparison of REE content with various petrographic facies in and near the Oklo reactors shows no apparent enrichment in fission product (intermediate) REE. With few exceptions, reactor facies all contain more REE than AOK. The chondrite-normalized REE pattern of AOK resembles that of greywacke-shale turbidites of Archean greenstone belts. The paucity of uranium and manganese in AOK is a curious anomaly in an area of world class uranium and manganese deposits.

  16. 7 CFR 550.16 - Project development.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 7 Agriculture 6 2013-01-01 2013-01-01 false Project development. 550.16 Section 550.16 Agriculture... § 550.16 Project development. REE provides partial funding to Cooperators to support research projects... the REE Agency's ADODR shall jointly develop the following documentation: (a) Project plan. A...

  17. 7 CFR 550.16 - Project development.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 7 Agriculture 6 2014-01-01 2014-01-01 false Project development. 550.16 Section 550.16 Agriculture... § 550.16 Project development. REE provides partial funding to Cooperators to support research projects... the REE Agency's ADODR shall jointly develop the following documentation: (a) Project plan. A...

  18. Rare earth element partitioning between hydrous ferric oxides and acid mine water during iron oxidation

    USGS Publications Warehouse

    Verplanck, P.L.; Nordstrom, D.K.; Taylor, H.E.; Kimball, B.A.

    2004-01-01

    Ferrous iron rapidly oxidizes to Fe (III) and precipitates as hydrous Fe (III) oxides in acid mine waters. This study examines the effect of Fe precipitation on the rare earth element (REE) geochemistry of acid mine waters to determine the pH range over which REEs behave conservatively and the range over which attenuation and fractionation occur. Two field studies were designed to investigate REE attenuation during Fe oxidation in acidic, alpine surface waters. To complement these field studies, a suite of six acid mine waters with a pH range from 1.6 to 6.1 were collected and allowed to oxidize in the laboratory at ambient conditions to determine the partitioning of REEs during Fe oxidation and precipitation. Results from field experiments document that even with substantial Fe oxidation, the REEs remain dissolved in acid, sulfate waters with pH below 5.1. Between pH 5.1 and 6.6 the REEs partitioned to the solid phases in the water column, and heavy REEs were preferentially removed compared to light REEs. Laboratory experiments corroborated field data with the most solid-phase partitioning occurring in the waters with the highest pH. ?? 2004 Elsevier Ltd. All rights reserved.

  19. The Presidential Address 2013: Promoting Enthusiasm, Imparting Knowledge! Science for the General Population and Science for Future Researchers Must All Start in the School Curriculum

    ERIC Educational Resources Information Center

    Rees, Martin

    2013-01-01

    This article provides a transcript of the Presidential Address delivered by Martin Rees, Lord Rees of Ludlow, to the Association for Science Education (ASE) Annual Conference at the University of Reading, January 2013. The address is divided into five sections under the following headings: (1) Three Reasons Why the ASE's Mission Is So…

  20. Rare earth element compositions of core sediments from the shelf of the South Sea, Korea: Their controls and origins

    NASA Astrophysics Data System (ADS)

    Jung, Hoi-Soo; Lim, Dhongil; Choi, Jin-Yong; Yoo, Hae-Soo; Rho, Kyung-Chan; Lee, Hyun-Bok

    2012-10-01

    Rare earth elements (REEs) of bulk sediments and heavy mineral samples of core sediments from the South Sea shelf, Korea, were analyzed to determine the constraints on REE concentrations and distribution patterns as well as to investigate their potential applicability for discriminating sediment provenance. Bulk sediment REEs showed large variation in concentrations and distribution patterns primarily due to grain size and carbonate dilution effects, as well as due to an abundance of heavy minerals. In the fine sandy sediments (cores EZ02-15 and 19), in particular, heavy minerals (primarily monazite and titanite/sphene) largely influenced REE compositions. Upper continental crust-normalized REE patterns of these sand-dominated sediments are characterized by enriched light REEs (LREEs), because of inclusion of heavy minerals with very high concentrations in LREEs. Notably, such a strong LREE enrichment is also observed in Korean river sediments. So, a great care must be taken when using the REE concentrations and distribution patterns of sandy and coarse silty shelf sediments as a proxy for discriminating sediment provenance. In the fine-grained muddy sediments with low heavy mineral abundance, in contrast, REE fractionation ratios and their UCC-normalized patterns seem to be reliable proxies for assessing sediment provenance. The resultant sediment origin suggested a long lateral transportation of some fine-grained Chinese river sediments (probably the Changjiang River) to the South Sea of Korea across the shelf of the northern East China Sea.

  1. Origin and distribution of rare earth elements in various lichen and moss species over the last century in France.

    PubMed

    Agnan, Y; Séjalon-Delmas, N; Probst, A

    2014-07-15

    Rare earth elements (REE) are known to be powerful environmental tracers in natural biogeochemical compartments. In this study, the atmospheric deposition of REE was investigated using various lichens and mosses as well as herbarium samples from 1870 to 1998 from six major forested areas in France. The comparison between the REE distribution patterns in organisms and bedrocks showed a regional uniformity influence from dust particles originating from the bedrock and/or soil weathering that were entrapped by lichens and mosses. These lithological signatures were consistent over the last century. The REE patterns of different organism species allowed minor influence of the species to be highlighted compared to the regional lithology. This was even true where the morphological features played a role in the bioaccumulation levels, which were related to the variable efficiency in trapping atmospheric dust particles. A comparison between REE profiles in the organisms and bark indicated a lack of influence of the substrate on lichen REE content. Lichens and mosses appear to be robust passive monitors of REE atmospheric deposition over decades because the mineral data was preserved in herbarium samples despite organic degradation being shown by carbon isotopes and SEM observations. To overcome the bias of REE concentration that resulted from organic degradation, the use of a normalized method is recommended to interpret the historical samples. PMID:24751590

  2. Analysis of the energy balance in lung cancer patients.

    PubMed

    Staal-van den Brekel, A J; Schols, A M; ten Velde, G P; Buurman, W A; Wouters, E F

    1994-12-15

    Previous studies have shown that an elevated resting energy expenditure (REE) frequently occurs in lung cancer patients. The aim of the present study was to assess the balance between REE and dietary intake and to analyze the contributing factors of elevated REE in newly detected lung cancer patients. One hundred newly detected lung cancer patients were evaluated. Measured values of REE were adjusted for the values predicted by the Harris-Benedict formula and for fat-free mass assessed by the bioelectrical impedance method. Dietary intake was measured using a dietary history. A substantial number of patients (30%) had a weight loss of 10% or more from their preillness stable weight. An elevated REE was found in 74% of the patients. Stratification by tumor localization revealed that patients with a central tumor had a significantly higher REE [121 +/- 13% (SD) versus 110 +/- 10% of predicted, P < 0.001] and significantly higher level of C-reactive protein (35 +/- 35 mg/liter versus 16 +/- 26 mg/liter, P = 0.006) compared with patients with a peripheral tumor. Dietary intake was significantly lower in the weight-losing group (1872 +/- 542 kcal/day versus 2169 +/- 782 kcal/day, P < 0.05) compared with the weight-stable group. We conclude that both elevated REE and decreased dietary intake contribute to weight loss in lung cancer patients. Tumor localization and inflammation were found to be contributing factors to the elevated REE. PMID:7987838

  3. Geochemistry of the rare earth elements in ferromanganese nodules from DOMES Site A, northern equatorial Pacific

    USGS Publications Warehouse

    Calvert, S.E.; Piper, D.Z.; Baedecker, P.A.

    1987-01-01

    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. ?? 1987.

  4. Planktonic foraminiferal rare earth elements as a potential new aeolian dust proxy

    NASA Astrophysics Data System (ADS)

    Chou, C.; Liu, Y.; Lo, L.; Wei, K.; Shen, C.

    2012-12-01

    Characteristics of rare earth elements (REEs) have widely been used as important tracers in many fields of earth sciences, including lithosphere research, environmental change, ocean circulation and other natural carbonate materials. Foraminiferal test REE signatures have been suggested to reflect ambient seawater conditions and serve as valuable proxies in the fields of paleoceanography and paleoclimate. Here we present a 60-kyr planktonic foraminifera Globigerinoides ruber (white, 250-300 μm) REE record of a sediment core MD05-2925 (9°20.61'S, 151°27.61'E, water depth 1660 m) from the Solomon Sea. The REE diagram shows two dominant sources of local seawater and nearby terrestrial input. The variability of foraminiferal REE/Ca time series is different from Mg/Ca-inferred sea surface temperature and δ18O records during the past 60-kyr. This inconsistency suggests that planktonic foraminiferal REE content cannot result only from changes in ice volume and temperature. Synchroneity between high planktonic foraminiferal REE content and Antarctic ice core dust amount record implies the same dust sources, probably from Australia or mainland China. Our results suggest that foraminiferal REE can potentially be as a new dust proxy and record dry/humid conditions at the source area.

  5. Development of a Rare Earth Element Paleoproxy

    NASA Astrophysics Data System (ADS)

    Haley, B. A.; Klinkhammer, G. P.; McManus, J.

    2002-12-01

    The rare earth elements (REEs) have demonstrated considerable potential as paleoproxies for changes in seawater chemistry. However, their utilization in paleoceanographic investigations has been mainly limited to neodymium isotopic analyses in metalliferous deposits and fossil apatite. The goal of being able to use the entire group of elements in foraminiferal shells has proven difficult. The problem with analysis of these elements in this matrix stems mainly from: (1) the ability to clean the shells of diagenetic aberrations and (2) the paucity of REE data in the environment where forams obtain their primary signature. We recently measured pore water profiles of REEs using an interfaced Ion Chromatograph (IC) and Inductively Coupled Plasma Mass Spectrometer (ICP-MS) in a depth transect off the Coast of California, and a profile from off the Peru-Chile margin. The pore water results are surprising and will alter our view of REE marine geochemistry. For example, they call into question the traditional method of calculating a "Ce-anomaly." The profiles also show dramatic changes in REE concentrations and patterns with depth, and demonstrate that the REE signature preserved in epifaunal benthic versus infaunal foram species and diagenetically added phases should be easily identifiable. Preliminary REE results from forams cleaned via a recently developed flow-through technique will be shown and compared to matching pore water data. We will conclude by outlining the potential of foraminiferal REE content for paleoceanography that ranges from water mass tracer to proxies for organic carbon flux and oxygen concentration.

  6. Rare earth element geochemistry and petrogenesis of miles (IIE) silicate inclusions

    NASA Astrophysics Data System (ADS)

    Hsu, Weibiao

    2003-12-01

    An ion probe study of rare earth element (REE) geochemistry of silicate inclusions in the Miles IIE iron meteorite was carried out. Individual mineral phases among inclusions have distinct REE patterns and abundances. Most silicate grains have homogeneous REE abundances but show considerable intergrain variations between inclusions. A few pyroxene grains display normal igneous REE zoning. Phosphates (whitlockite and apatite) are highly enriched in REEs (50 to 2000 × CI) with a relatively light rare earth element (LREE)-enriched REE pattern. They usually occurred near the interfaces between inclusions and Fe host. In Miles, albitic glasses exhibit two distinctive REE patterns: a highly fractionated LREE-enriched (CI normalized La/Sm ˜15) pattern with a large positive Eu anomaly and a relatively heavy rare earth element (HREE)-enriched pattern (CI-normalized Lu/Gd ˜4) with a positive Eu anomaly and a negative Yb anomaly. The glass is generally depleted in REEs relative to CI chondrites. The bulk REE abundances for each inclusion, calculated from modal abundances, vary widely, from relatively depleted in REEs (0.1 to 3 × CI) with a fractionated HREE-enriched pattern to highly enriched in REEs (10 to 100 × CI) with a relatively LREE-enriched pattern. The estimated whole rock REE abundances for Miles are at ˜ 10 × CI with a relatively LREE-enriched pattern. This implies that Miles silicates could represent the product of a low degree (˜10%) partial melting of a chondritic source. Phenocrysts of pyroxene in pyroxene-glassy inclusions were not in equilibrium with coexisting albitic glass and they could have crystallized from a parental melt with REEs of ˜ 10 × CI. Albitic glass appears to have formed by remelting of preexisting feldspar + pyroxene + tridymite assemblage. Yb anomaly played an important role in differentiation processes of Miles silicate inclusions; however, its origin remains unsolved. The REE data from this study suggest that Miles, like

  7. Rare Earth Element Measurements of Melilite and Fassaite in Allende Cai by Nanosims

    NASA Technical Reports Server (NTRS)

    Ito, M.; Messenger, Scott

    2009-01-01

    The rare earth elements (REEs) are concentrated in CAIs by approx. 20 times the chondritic average [e.g., 1]. The REEs in CAIs are important to understand processes of CAI formation including the role of volatilization, condensation, and fractional crystallization [1,2]. REE measurements are a well established application of ion microprobes [e.g., 3]. However the spatial resolution of REE measurements by ion microprobe (approx.20 m) is not adequate to resolve heterogeneous distributions of REEs among/within minerals. We have developed methods for measuring REE with the NanoSIMS 50L at smaller spatial scales. Here we present our initial measurements of REEs in melilite and fassaite in an Allende Type-A CAI with the JSC NanoSIMS 50L. We found that the key parameters for accurate REE abundance measurements differ between the NanoSIMS and conventional SIMS, in particular the oxide-to-element ratios, the relative sensitivity factors, the energy distributions, and requisite energy offset. Our REE abundance measurements of the 100 ppm REE diopside glass standards yielded good reproducibility and accuracy, 0.5-2.5 % and 5-25 %, respectively. We determined abundances and spatial distributions of REEs in core and rim within single crystals of fassaite, and adjacent melilite with 5-10 m spatial resolution. The REE abundances in fassaite core and rim are 20-100 times CI abundance but show a large negative Eu anomaly, exhibiting a well-defined Group III pattern. This is consistent with previous work [4]. On the other hand, adjacent melilite shows modified Group II pattern with no strong depletions of Eu and Yb, and no Tm positive anomaly. REE abundances (2-10 x CI) were lower than that of fassaite. These patterns suggest that fassaite crystallized first followed by a crystallization of melilite from the residual melt. In future work, we will carry out a correlated study of O and Mg isotopes and REEs of the CAI in order to better understand the nature and timescales of its

  8. Residual levels of rare earth elements in freshwater and marine fish and their health risk assessment from Shandong, China.

    PubMed

    Yang, Luping; Wang, Xining; Nie, Hongqian; Shao, Lijun; Wang, Guoling; Liu, Yongjun

    2016-06-15

    The total concentrations of rare earth elements (ΣREE) were quantified in 251 samples from 10 common species of freshwater and marine fish in seventeen cities of Shandong, China. ΣREE obtained from the freshwater fish ranged from 34.0 to 37.9ngg(-1) (wet weight) and marine fish from 12.7 to 37.6ngg(-1). The ratio of LREE to HREE was 13.7:1 and 10:1 for freshwater and marine fish, respectively. This suggests that freshwater fish exhibit greater REE concentrations than marine fish and the biological effects of LREE are higher than HREE. Results revealed a similar REE distribution pattern between those fish and coastal sediments, abiding the "abundance law". The health risk assessment demonstrated the EDIs of REEs in fish were significantly lower than the ADI, indicating that the consumption of these fish presents little risk to human health. PMID:27016961

  9. Changes in Resting Energy Expenditure in Relation to Body Weight and Composition Following Gastric Restriction: A Systematic Review.

    PubMed

    Browning, Matthew G; Franco, Robert L; Cyrus, John C; Celi, Francesco; Evans, Ronald K

    2016-07-01

    In comparison to gastric bypass surgery, gastric restriction without malabsorption more closely simulates dietary adherence while still producing durable weight loss. The latter is achieved despite considerable reductions in resting energy expenditure (REE), and whether REE is adjusted for body weight/composition using ratio- or regression-based methods could influence understanding of how these procedures affect energy balance. This systematic review identified studies that reported REE before and after gastric restriction in order to compare changes using each method. Ratio assessments revealed increases and decreases when REE was expressed per kilogram of body weight and per kilogram of fat-free mass, respectively. In comparison, measured REE tended to be less than predicted from linear regression after surgery. Explanations for these seemingly disparate findings and future directions are discussed. PMID:27103027

  10. Distribution and Geochemistry of Rare-Earth Elements in Rivers of Southern and Eastern Primorye (Far East of Russia)

    NASA Astrophysics Data System (ADS)

    Chudaev, O. V.; Bragin, I. V.; A, Kharitonova N.; Chelnokov, G. A.

    2016-03-01

    The distribution and geochemistry of rare earth elements (REE) in anthropogenic, technogenic and natural surface waters of southern and eastern Primorye, Far East of Russia, are presented in this study. The obtained results indicated that most of REE (up to 70%) were transported as suspended matter, ratio between dissolved and suspended forms varing from the source to the mouth of rivers. It is shown that all REE (except Ce) in the source of the rivers are predominantly presented in dissolved form, however, the content of light and heavy REE is different. Short-term enrichment of light rare earth elements (LREE) caused by REE-rich runoff from waste dumps and mining is neutralized by the increase in river flow rate. Rivers in urban areas are characterized by high content of LREE in dissolved form and very low in suspended one.

  11. Échange terres rares légères Ca dans l'apatite

    NASA Astrophysics Data System (ADS)

    Iqdari, Abderrahmane; Velde, Bruce; Benalioulhaj, Noureddine; Dujon, Saint-Clair; El Yamine, Nacer

    2003-04-01

    Diffusion experiments were carried out on natural apatite crystals that were immersed in molten light rare earth element (REE) chloride salt at temperatures between 900 and 1150 °C for periods up to 35 days. Electron microprobe analysis of the crystals showed that light REEs replaced Ca according to electronic balance, i.e. 2 REE3+ for 3 Ca2+. These diffusion profiles indicate that a maximum amount of substitution in the structure occurs when two of the ten Ca ions in apatite are replaced by the REE diffusing elements. Anisotropic diffusion is observed between a and c crystallographic directions. Comparison of maximum distance indicates that the larger ions move more easily in the apatite structure. We conclude that the light REEs diffuse within the channel structures of the mineral, and that this diffusion is controlled by the substitution type of elements in the calcium sites. To cite this article: A. Iqdari et al., C. R. Geoscience 335 (2003).

  12. Phosphates in pallasite meteorites as probes of mantle processes in small planetary bodies

    NASA Technical Reports Server (NTRS)

    Davis, Andrew M.; Olsen, Edward J.

    1991-01-01

    Trace element analyses of the phosphates minerals in stony-iron pallasite meteorites are used here to investigate the magmatic history of the silicate portions of pallasites. In Eagle Station and seven other pallasites, the phosphates have relatively low concentrations of REEs and are strongly enriched in heavy relative to light REE. These patterns are consistent with formation of phosphate by subsolidus reactions between metal and silicate, in which phosphate inherits the REE pattern of olivine. In Springwater and Santa Rosalia, calcium-rich phosphates have higher concentrations of REE, are enriched in light relative to heavy REE, and have negative europium anomalies. These patterns are consistent with crystallization of phosphate from a europium-depleted chondritic liquid. This is unlikely to have happened near the base of the differentiating parent-body mantle; it suggests that some pallasites may come from regions of their parent bodies much nearer the surface than the core-mantle boundary.

  13. Uncovering the Global Life Cycles of the Rare Earth Elements

    PubMed Central

    Du, Xiaoyue; Graedel, T. E.

    2011-01-01

    The rare earth elements (REE) are a group of fifteen elements with unique properties that make them indispensable for a wide variety of emerging, critical technologies. Knowledge of the life cycles of REE remains sparse, despite the current heightened interest in their future availability. Mining is heavily concentrated in China, whose monopoly position and potential restriction of exports render primary supplies vulnerable to short and long-term disruption. To provide an improved perspective we derived the first quantitative life cycles (for the year 2007) for ten REE: lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), and yttrium (Y). Of these REE, Ce and Nd in-use stocks are highest; the in-use stocks of most REE show significant accumulation in modern society. Industrial scrap recycling occurs only from magnet manufacture. We believe there is no post-customer recycling of any of these elements. PMID:22355662

  14. The Effect of Organic Ligands on the Sorption of Neodymium, Gadolinium and Uranium onto Nontronite and Goethite

    SciTech Connect

    Scott A. Wood

    2007-06-12

    The sorption of the rare earth elements (REE) Nd(III) and Gd(III) onto goethite in the presence of Suwannee River fulvic acid in 0.1 m NaCl solutions at 25 ºC was investigated quantitatively. The experiments involved batch titrations whereby the concentrations of REE and/or fulvic acid remaining in solution were determined as a function of pH. In the absence of fulvic acid, removal of REE from solution is enhanced in the presence of goethite over the pH range from 6 to 8, compared to the unary system (REE only) in which precipitation of an amorphous hydroxide occurred at pH greater than or equal to 8. In the absence of REE, removal of fulvic acid from solution is enhanced in the presence of goethite in the pH range from 2 to 8 at least 9, compared to a unary (fulvic acid only) system. The presence of fulvic acid at concentrations from 10 to 50 ppm enhanced REE sorption onto goethite slightly at pH less than 7, but had no discernable effect at higher pH values. Fulvic acid at a concentration of 100 ppm exhibited a greater enhancement of REE sorption at pH < 7, but inhibited REE sorption slightly at pH > 7. Experiments investigating the effect of sorption of REE onto goethite by citrate were also performed. However, these studies were not completed owing to experimental difficulties. The results obtained in this study represent an important contribution to the ultimate goal of predicting the mobility of trivalent REE (and analogous trivalent actinides) in the presence of natural organic matter and goethite.

  15. Isotopic fractionation of rare earth elements in geochemical samples

    NASA Astrophysics Data System (ADS)

    Ishibashi, T.; Ohno, T.

    2015-12-01

    The isotopic composition of Rare Earth Elements(REEs) can be fractionated through various physical and chemical reactions in nature [1]. The isotopic variations of REEs occurring naturally has a potentially significant influence in geochemical research fields. The REEs has key features that their chemical similarities and gradual changes of ionic radius, which may help us to understand the mechanisms of isotopic variations of REEs in nature. Among the REEs, geochemical and physicochemical features of Ce, which could be presence as the tetravalent state, be anomalous, and oxidation state of Ce can change by reflecting the redox conditions of the environment. Therefore, the study of the difference in the degree of isotopic fractionation between Ce and other REEs may provide information on the redox conditions. In this study, we developed a new separation method to determine the mass-dependent isotopic fractionations of REEs in geochemical samples, and examined the optimum concentration of hydrochloric acid for the separation. The samples were decomposed by a mixture of acids, then REEs were separated as a group from major elements using cation exchange resin columns and RE Spec resin. The separations within the REEs group were carried out using Ln2Spec resin. For the recovery of La, Ce, Pr, and Nd, 0.1 M HCl was used, and for isolation of Sm, Eu, and Gd, 0.25 M HCl was used. Then, 0.6 M HCl was used for separation of Tb, and Dy, 1 M HCl was used for separation of Ho, Y, and Er, finally, Tm, Yb, and Lu were collected using 2 M HCl. The yields of all REEs were enough to examine isotopic fractionation in geochemical samples. [1] Ohno and Hirata,Analytical Sciences, 29, 271, 2013

  16. Using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) to explore geochemical taphonomy of vertebrate fossils in the upper cretaceous two medicine and Judith River formations of Montana

    USGS Publications Warehouse

    Rogers, R.R.; Fricke, H.C.; Addona, V.; Canavan, R.R.; Dwyer, C.N.; Harwood, C.L.; Koenig, A.E.; Murray, R.; Thole, J.T.; Williams, J.

    2010-01-01

    Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) was used to determine rare earth element (REE) content of 76 fossil bones collected from the Upper Cretaceous (Campanian) Two Medicine (TMF) and Judith River (JRF) Formations of Montana. REE content is distinctive at the formation scale, with TMF samples exhibiting generally higher overall REE content and greater variability in REE enrichment than JRF samples. Moreover, JRF bones exhibit relative enrichment in heavy REE, whereas TMF bones span heavy and light enrichment fields in roughly equal proportions. TMF bones are also characterized by more negative Ce anomalies and greater U enrichment than JRF bones, which is consistent with more oxidizing diagenetic conditions in the TMF. Bonebeds in both formations show general consistency in REE content, with no indication of spatial or temporal mixing within sites. Previous studies, however, suggest that the bonebeds in question are attritional assemblages that accumulated over considerable time spans. The absence of geochemical evidence for mixing is consistent with diagenesis transpiring in settings that remained chemically and hydrologically stable during recrystallization. Lithology-related patterns in REE content were also compared, and TMF bones recovered from fluvial sandstones show relative enrichment in heavy REE when compared with bones recovered from fine-grained floodplain deposits. In contrast, JRF bones, regardless of lithologic context (sandstone versus mudstone), exhibit similar patterns of REE uptake. This result is consistent with previous reconstructions that suggest that channel-hosted microfossil bonebeds of the JRF developed via the reworking of preexisting concentrations embedded in the interfluve. Geochemical data further indicate that reworked elements were potentially delivered to channels in a recrystallized condition, which is consistent with rapid adsorption of REE postmortem. Copyright ?? 2010, SEPM (Society for

  17. Rare Earth Element Transfer from Soil to Navel Orange Pulp (Citrus sinensis Osbeck cv. Newhall) and the Effects on Internal Fruit Quality

    PubMed Central

    Cheng, Jinjin; Ding, Changfeng; Li, Xiaogang; Zhang, Taolin; Wang, Xingxiang

    2015-01-01

    The effects of soil rare earth element (REE) on navel orange quality and safety in rare earth ore areas have gained great attention. This study investigated the transfer characteristics of REE from soil to navel orange pulp (Citrus sinensis Osbeck cv. Newhall) and examined the effects of soil REE on internal fruit quality in Xinfeng County, Jiangxi province, China. Path analysis showed that soil REE, pH, cation exchange capacity (CEC), and Fe oxide (Feox) significantly affected pulp REE concentrations. A Freundlich-type prediction model for pulp REE was established: log[REEpulp] = -1.036 + 0.272 log[REEsoil] - 0.056 pH - 0.360 log[CEC] + 0.370 log[Feox] (n = 114, R2 = 0.60). From the prediction model, it was inferred that even when soil REE and Feox were as high as 1038 mg kg-1 and 96.4 g kg-1, respectively, and pH and CEC were as low as 3.75 and 5.08 cmol kg-1, respectively, pulp REE concentrations were much lower than the food limit standard. Additionally, soil REE levels were significantly correlated with selected fruit quality indicators, including titratable acidity (r = 0.52, P < 0.01), total soluble solids (r = 0.48, P < 0.01) and vitamin C (r = 0.56, P < 0.01). Generally, under routine methods of water and fertilization management, the cultivation of navel oranges in rare earth ore areas of south China with soil REE ranging from 38.6 to 546 mg kg-1 had improved in internal fruit quality. PMID:25806821

  18. Transfer of rare earth elements from natural metalliferous (copper and cobalt rich) soils into plant shoot biomass of metallophytes from Katanga (Democratic Republic of Congo)

    NASA Astrophysics Data System (ADS)

    Pourret, Olivier; Lange, Bastien; Jitaru, Petru; Mahy, Grégory; Faucon, Michel-Pierre

    2014-05-01

    The geochemical behavior of rare earth elements (REE) is generally assessed for the characterization of the geological systems where these elements represent the best proxies of processes involving the occurrence of an interface between different media. REE behavior is investigated according to their concentrations normalized with respect to the upper continental crust. In this study, the geochemical fingerprint of REE in plant shoot biomass of an unique metallicolous flora (i.e., Crepidorhopalon tenuis and Anisopappus chinensis) was investigated. The plants originate from extremely copper and cobalt rich soils, deriving from Cu and Co outcrops in Katanga, Democratic Republic of Congo. Some of the species investigated in this study are able to accumulate high amounts of Cu and Co in shoot hence being considered as Cu and Co hyperaccumulators. Therefore, assessing the behavior of REE may lead to a better understanding of the mechanisms of metal accumulation by this flora. The data obtained in this study indicate that REE uptake by plants is not primarily controlled by their concentration and speciation in the soil as previously shown in the literature (Brioschi et al. 2013). Indeed, the REE patterns in shoots are relatively flat whereas soils patterns are Middle REE enriched. In addition, it is worth noting that Eu enrichments occur in aerial parts of the plants. These positive Eu anomalies suggest that Eu3 + can form stable organic complexes replacing Ca2 + in several biological processes as in xylem fluids associated with the general nutrient flux. Therefore, is is possible that the Eu mobility in these fluids is enhanced by its reductive speciation as Eu2 +. Eventually, the geochemical behavior of REE illustrates that metals accumulation in aerial parts of C. tenuis and A. chinensis is mainly driven by dissolved complexation. Brioschi, L., Steinmann, M., Lucot, E., Pierret, M., Stille, P., Prunier, J., Badot, P., 2013. Transfer of rare earth elements (REE) from

  19. Chemical equilibria of rare earth oxides in glow-discharge mass spectrometry

    SciTech Connect

    Mei, Y.

    1992-01-01

    This research centers around method development and fundamental exploration of the rare earth elements (REE) in glow discharge mass spectrometry (GDMS). The capability of GDMS to analyze directly solids materials eliminates the sample dissolution and preconcentration steps required by many other methods. The simplicity of sample preparation and instrumental operation makes GDMS a promising analytical technique for the field of earth science. Initial studies were dedicated to improving the detection sensitivity of GDMS in analyzing the REE. This was accomplished by eliminating water contamination, a factor that was found to prevent the conversion of the rare earth oxidized to their atomic form in the glow discharge plasma. Methods experimented for water elimination included the uses of both a cryogenic cooling device and getter reagents. When used to determine the REE concentrations in a standard rock sample, the chemical elimination approach yielded comparable results to that obtained by other analytical methods. Further studies focused on probing the chemical reactions involving the REE and other plasma constituents in the glow discharge. It is proposed that the availability of the atomic REE in the glow discharge is strongly influenced by the oxidant and reductant contents in the plasma. Species that contain oxygen tend to shift the redox equilibria of REE toward the formation of their oxides, whereas species that compete for oxygen help reduce the oxidant content in the plasma, and shift the REE redox equilibria toward the formation of the REE atoms. Factors that govern the reaction processes of the REE equilibria were investigated by means of plasma reagent introduction and time-resolved discharge operation. Results indicate that while redox equilibria between the elemental REE and their monoxides exist on the cathode surface and in the gas phase, interactions occurring in the gas phase are probably the main paths for this equilibration in the glow discharge.

  20. Lunar ferroan anorthosite petrogenesis: clues from trace element distributions in FAN subgroups

    USGS Publications Warehouse

    Floss, C.; James, O.B.; McGee, J.J.; Crozaz, G.

    1998-01-01

    The rare earth elements (REE) and selected other trace elements were measured in plagioclase and pyroxene from nine samples of the lunar ferroan anorthosite (FAN) suite of rocks. Samples were selected from each of four FAN subgroups previously defined by James et al. (1989). Plagioclase compositions are homogeneous within each sample, but high- and low-Ca pyroxenes from lithic clasts typically have different REE abundances from their counterparts in the surrounding granulated matrices. Measured plagioclase/low-Ca pyroxene concentration ratios for the REE have steeper patterns than experimentally determined plagioclase/low-Ca pyroxene partition coefficients in most samples. Textural and trace element evidence suggest that, although subsolidus equilibration may be responsible for some of the discrepancy, plagioclase compositions in most samples have been largely unaffected by intermineral redistribution of the REE. The REE systematics of plagioclase from the four subgroups are broadly consistent with their deviation through crystallization from a single evolving magma. However, samples from some of the subgroups exhibit a decoupling of plagioclase and pyroxene compositions that probably reflects the complexities inherent in crystallization from a large-scale magmatic system. For example, two anorthosites with very magnesian mafic minerals have highly evolved trace element compositions; major element compositions in plagioclase also do not reflect the evolutionary sequence recorded by their REE compositions. Finally, a noritic anorthosite breccia with relatively ferroan mafic minerals contains several clasts with high and variable REE and other trace element abundances. Although plagioclase REE compositions are consistent with their derivation from a magma with a KREEPy trace element signature, very shallow REE patterns in the pyroxenes suggest the addition of a component enriched in the light REE.

  1. Rare earth element transfer from soil to navel orange pulp (Citrus sinensis Osbeck cv. Newhall) and the effects on internal fruit quality.

    PubMed

    Cheng, Jinjin; Ding, Changfeng; Li, Xiaogang; Zhang, Taolin; Wang, Xingxiang

    2015-01-01

    The effects of soil rare earth element (REE) on navel orange quality and safety in rare earth ore areas have gained great attention. This study investigated the transfer characteristics of REE from soil to navel orange pulp (Citrus sinensis Osbeck cv. Newhall) and examined the effects of soil REE on internal fruit quality in Xinfeng County, Jiangxi province, China. Path analysis showed that soil REE, pH, cation exchange capacity (CEC), and Fe oxide (Feox) significantly affected pulp REE concentrations. A Freundlich-type prediction model for pulp REE was established: log[REEpulp] = -1.036 + 0.272 log[REEsoil] - 0.056 pH - 0.360 log[CEC] + 0.370 log[Feox] (n = 114, R2 = 0.60). From the prediction model, it was inferred that even when soil REE and Feox were as high as 1038 mg kg-1 and 96.4 g kg-1, respectively, and pH and CEC were as low as 3.75 and 5.08 cmol kg-1, respectively, pulp REE concentrations were much lower than the food limit standard. Additionally, soil REE levels were significantly correlated with selected fruit quality indicators, including titratable acidity (r = 0.52, P < 0.01), total soluble solids (r = 0.48, P < 0.01) and vitamin C (r = 0.56, P < 0.01). Generally, under routine methods of water and fertilization management, the cultivation of navel oranges in rare earth ore areas of south China with soil REE ranging from 38.6 to 546 mg kg-1 had improved in internal fruit quality. PMID:25806821

  2. Efficient mobilization and fractionation of rare-earth elements by aqueous fluids upon slab dehydration

    NASA Astrophysics Data System (ADS)

    Tsay, A.; Zajacz, Z.; Sanchez-Valle, C.

    2014-07-01

    The characteristic REE fractionation pattern in arc magmas compared to MOR-basalts results from the selective mobilization of light rare-earth elements (LREE) by slab-derived mobile components. However, the nature and composition of the slab flux, and the actual mechanisms responsible for the transfer of rare-earth elements (REE) from the slab to the mantle wedge remain unclear. We present experimental data on the solubility of selected REE in ligand-bearing aqueous fluids and a hydrous haplogranitic melt at 2.6 GPa and 600-800 °C, spanning the conditions relevant to slab dehydration and melting. The solubilities of REE in aqueous fluids increase more than an order of magnitude with temperature increasing from 600 to 800 °C. Addition of ligands such as Cl-, F-, CO32-, SO42- in relatively small concentrations (0.3-1.5 m [mol/kg H2O]) has a pronounced effect further enhancing REE solubilities. Each ligand yields a characteristic REE pattern by preferential dissolution of either the light or the heavy REE. For example, the addition of NaCl to the aqueous fluids yields highly elevated LREE/HREE ratios (La/Yb=17.4±4.3), whereas the addition of fluoride and sulfate ligands significantly increases the solubility of all REE with moderate LREE/HREE fractionation (La/Yb∼4). The addition of Na2CO3 results in preferential increase of HREE solubilities, and yields La/Yb ratio of 1.6±0.5 by flattening the moderately fractionated REE pattern seen in pure aqueous fluids. The solubilities in hydrous haplogranite melt are moderate in comparison to those observed in aqueous fluids and do not lead to pronounced REE fractionation. Therefore, REE can be effectively mobilized and fractionated by aqueous fluids, compared to felsic hydrous melts. Furthermore, the aqueous fluid chemistry has a major role in determining REE mobilities and fractionation upon slab dehydration in addition to the significant control exerted by temperature. Our results show that chloride-bearing slab

  3. Rare earth elements in the Amazon basin

    NASA Astrophysics Data System (ADS)

    Gerard, M.; Seyler, P.; Benedetti, M. F.; Alves, V. P.; Boaventura, G. R.; Sondag, F.

    2003-05-01

    The rare earth element (REE) concentrations of the dissolved and particulate fractions and bed sediment between Manaus and Santarém in the Amazon River, and in some major tributaries, were evaluated. A very important zone in the Amazon basin, the encontro das aguas area where the Rio Solimões and the Rio Negro meet, was especially sampled. Different size fractions were isolated by ultrafiltration. Water samples were collected at different stages of the mixing. Three groups of waters are distinguished: group I has a low pH (<5·5) and is represented by the Negro basin rivers; group II has alkalinity less than 0·2 meq l-1 and is represented by the Rios Tapajós and Trombetas; group III has high alkalinity (>0·2 meq l-1) and higher pH (>6·5) and is represented by the Madeira basin rivers, the Solimões and the Amazon. The highest dissolved REE concentration is in the Rio Negro and the lowest in the Rio Tapajós (dissolved REEs vary by more than a factor of ten). The solubility of REEs is pH dependent: in river waters with a pH < 6 the Ce concentration is twice that of La, whereas in rivers with a higher pH the concentrations of Ce and La are similar. Dissolved REE concentrations are positively correlated with the dissolved organic carbon. Correlations between Fe, Al, and La suggest that La is associated with Al (Fe)-rich organic matter and/or related to dissolved Fe-rich inorganic material. Dissolved REEs normalized to North American shale composite show an enrichment in intermediate/heavy REEs (from Eu to Er), except for the shields rivers (such as Rio Negro and Rio Trombetas). Both of them are depleted in heavy REEs and show a relative Ce enrichment. In contrast, for the Andeans rivers (such as Rio Solimões), light REEs are slightly depleted and a negative Ce relative anomaly occurs. The pattern of the Amazon River at Óbidos confirms the major influence of the Rios Negro and Solimões with REE fractionation. For the Rio Negro, 60 to 70% of REEs are

  4. Binding and transport of rare earth elements by organic and iron-rich nanocolloids in Alaskan rivers, as revealed by field-flow fractionation and ICP-MS

    NASA Astrophysics Data System (ADS)

    Stolpe, Björn; Guo, Laodong; Shiller, Alan M.

    2013-04-01

    Water samples were collected from six small rivers in the Yukon River basin in central Alaska to examine the role of nanocolloids (0.5-40 nm) in the dynamics and transport of rare earth elements (REEs) in northern high latitude watersheds influenced by permafrost. Total dissolved (<0.45 μm) concentrations and the 'nanocolloidal size distributions' (0.5-40 nm) of UV-absorbing dissolved organic matter, Fe, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu were determined by on-line coupling of flow field-flow fractionation (FFF) with a UV-absorbance detector and ICP-MS. Total dissolved and nanocolloidal concentrations of the REEs co-varied with dissolved organic carbon (DOC) in all rivers and between spring flood and late summer baseflow. The nanocolloidal size distributions indicated the presence of three major components of nanocolloids: the 0.5-3 nm 'fulvic-rich nanocolloids' occurring throughout the sampling season, the 'organic/iron-rich nanocolloids' residing in the <8 nm size range during the spring flood, and the 4-40 nm iron-rich nanocolloids occurring during summer baseflow. REEs associated with all the three components of nanocolloids, but the proportions associated with the fulvic-rich nanocolloids during summer baseflow increased with increasing REE molar mass, which is consistent with the increase in stability of organic REE-complexes with increasing REE molar mass. Normalization of the measured REE-concentrations with the average REE-concentrations of the upper continental crust revealed a dynamic change in the physicochemical fractionation of REEs. During the spring flood, REE-binding in all the rivers was dominated by the <8 nm organic/iron-rich nanocolloids, likely being eroded from the upper organic-rich soil horizon by the strong surface runoff of snowmelt water. During the summer, the REE-binding in rivers with large groundwater input was dominated by small (<0.5 nm) organic and/or inorganic complexes, while lower proportions of the REEs

  5. An EDTA-β-cyclodextrin material for the adsorption of rare earth elements and its application in preconcentration of rare earth elements in seawater.

    PubMed

    Zhao, Feiping; Repo, Eveliina; Meng, Yong; Wang, Xueting; Yin, Dulin; Sillanpää, Mika

    2016-03-01

    The separation and recovery of Rare earth elements (REEs) from diluted aqueous streams has attracted great attention in recent years because of ever-increasing REEs demand. In this study, a green synthesized EDTA-cross-linked β-cyclodextrin (EDTA-β-CD) biopolymer was prepared and employed in adsorption of aqueous REEs, such as La(III), Ce(III), and Eu(III). EDTA acts not only as cross-linker but also as coordination site for binding of REEs. The adsorption properties for the adsorption of REEs by varying experimental conditions were carried out by batch tests. The kinetics results revealed that the surface chemical sorption and the external film diffusion were the rate-determining steps of the adsorption process. The obtained maximum adsorption capacities of EDTA-β-CD were 0.343, 0.353, and 0.365mmolg(-1) for La(III), Ce(III) and Eu(III), respectively. Importantly, the isotherms fitted better to Langmuir than Freundlich and Sips models, suggesting a homogenous adsorption surface for REEs on the adsorbent. Moreover, the multi-component adsorption, which was modeled by extended Sips isotherms, revealed adsorbent's selectivity to Eu(III). More significantly, the successful recoveries of the studied ions from tap water and seawater samples makes EDTA-β-CD a promising sorbent for the preconcentration of REEs from diluted aqueous streams. PMID:26674238

  6. An improved description of the interactions between rare earth elements and humic acids by modeling: PHREEQC-Model VI coupling

    NASA Astrophysics Data System (ADS)

    Marsac, Rémi; Davranche, Mélanie; Gruau, Gérard; Bouhnik-Le Coz, Martine; Dia, Aline

    2011-10-01

    The Humic Ion Binding Model VI (Model VI) - previously used to model the equilibrium binding of rare earth elements (REE) by humic acid (HA) - was modified to account for differences in the REE constant patterns of the HA carboxylic and phenolic groups, and introduced into PHREEQC to calculate the REE speciation on the HA binding sites. The modifications were shown to greatly improve the modeling. They allow for the first time to both satisfactorily and simultaneously model a large set of multi-REE experimental data with the same set of equations and parameters. The use of PHREEQC shows that the light rare earth elements (LREE) and heavy rare earth elements (HREE) do not bind to HA by the same functional groups. The LREE are preferentially bound to carboxylic groups, whereas the HREE are preferentially bound to carboxy-phenolic and phenolic groups. This binding differentiation might lead to a fractionation of REE-HA patterns when competition between REE and other metals occur during complexation. A survey of the available data shows that competition with Al 3+ could lead to the development of HREE-depleted HA patterns. This new model should improve the hydrochemical modeling of the REE since PHREEQC takes into account chemical reactions such as mineral dissolution/precipitation equilibrium and redox reactions, but also models kinetically controlled reactions and one-dimensional transport.

  7. Innovative Application of Mechanical Activation for Rare Earth Elements Recovering: Process Optimization and Mechanism Exploration

    NASA Astrophysics Data System (ADS)

    Tan, Quanyin; Deng, Chao; Li, Jinhui

    2016-01-01

    With the rapidly expanding use of fluorescent lamps (FLs) and increasing interest in conservation and sustainable utilization of critical metals such as rare earth elements (REEs), the recovering of REEs from phosphors in waste FLs is becoming a critical environmental and economic issue. To effectively recycle REEs with metallurgical methods, mechanical activation by ball milling was introduced to pretreat the waste phosphors. This current study put the emphasis on the mechanical activation and leaching processes for REEs, and explored the feasibility of the method from both theoretical and practical standpoints. Results showed physicochemical changes of structural destruction and particle size reduction after mechanical activation, leading to the easy dissolution of REEs in the activated samples. Under optimal conditions, dissolution yields of 89.4%, 93.1% and 94.6% for Tb, Eu and Y, respectively, were achieved from activated waste phosphors using hydrochloric acid as the dissolution agent. The shrinking core model proved to be the most applicable for the leaching procedure, with an apparent activation energy of 10.96 ± 2.79 kJ/mol. This novel process indicates that mechanical activation is an efficient method for recovering REEs from waste phosphors, and it has promising potential for REE recovery with low cost and high efficiency.

  8. Rare earth element measurements and mapping of minerals in the Allende CAI, 7R19-1, by NanoSIMS ion microprobe

    NASA Astrophysics Data System (ADS)

    Ito, Motoo; Messenger, Scott

    2016-04-01

    We have established analytical procedures for quantitative rare earth element (REE) measurements by NanoSIMS 50L ion microprobe with 2-10 μm spatial resolution. Measurements are performed by multidetection using energy filtering under several static magnetic field settings. Relative sensitivity factors and REE oxide/REE element secondary ion ratios that we determined for the NanoSIMS match values previously determined for other ion microprobes. REE measurements of 100 ppm REE glass standards yielded reproducibility and accuracy of 0.5-2.5% and 5-15%, respectively. REE measurements of minerals of an Allende type-A CAI, 7R19-1, were performed using three different methods: spot analysis, line profile, and imaging. These data are in excellent agreement with previous REE measurements of this inclusion by IMS-3f ion microprobe. The higher spatial resolution NanoSIMS measurements provide additional insight into the formation process of this CAI and offer a promising new tool for analysis of fine-grained and complexly zoned materials.

  9. Rare earth element mobility in vesicular lava during low-grade metamorphism

    NASA Astrophysics Data System (ADS)

    Nyström, Jan Olov

    1984-12-01

    A geochemical comparison of basaltic relicts and spilitic domains from two burial metamorphosed flows in central Chile, of similar original composition and rich and poor in amygdules, respectively, demonstrates a relationship between initial vesicularity and rare earth element (REE) mobility. During spilitization the REE were partly leached from permeable parts of the flows and precipitated in voids, now amygdules and veinlets. The REE (excluding Eu) moved coherently in the highly amygdaloidal flow: spilitic domains and amygdules inherited the basaltic REE pattern. Besides being characterized by a positive Eu anomaly, epidotes separated from amygdules have a REE distribution which mimics that of the basalt; the absolute contents range widely, suggesting local and/or temporal REE variations in the metamorphic fluids. Pumpellyite differs by being strongly enriched in heavy REE. Similar ratios of Th, Hf and Ta in samples as contrasting as relict basalt and a geode are consistent with coherent leaching. Coherent mobility, when established for a rock system, can be used to elucidate, for example, whether minerals in cross-cutting veins were formed by local redistribution or from introduced material.

  10. Innovative Application of Mechanical Activation for Rare Earth Elements Recovering: Process Optimization and Mechanism Exploration.

    PubMed

    Tan, Quanyin; Deng, Chao; Li, Jinhui

    2016-01-01

    With the rapidly expanding use of fluorescent lamps (FLs) and increasing interest in conservation and sustainable utilization of critical metals such as rare earth elements (REEs), the recovering of REEs from phosphors in waste FLs is becoming a critical environmental and economic issue. To effectively recycle REEs with metallurgical methods, mechanical activation by ball milling was introduced to pretreat the waste phosphors. This current study put the emphasis on the mechanical activation and leaching processes for REEs, and explored the feasibility of the method from both theoretical and practical standpoints. Results showed physicochemical changes of structural destruction and particle size reduction after mechanical activation, leading to the easy dissolution of REEs in the activated samples. Under optimal conditions, dissolution yields of 89.4%, 93.1% and 94.6% for Tb, Eu and Y, respectively, were achieved from activated waste phosphors using hydrochloric acid as the dissolution agent. The shrinking core model proved to be the most applicable for the leaching procedure, with an apparent activation energy of 10.96 ± 2.79 kJ/mol. This novel process indicates that mechanical activation is an efficient method for recovering REEs from waste phosphors, and it has promising potential for REE recovery with low cost and high efficiency. PMID:26819083

  11. Lanthanide and actinide chemistry at high C/O ratios in the solar nebula

    NASA Astrophysics Data System (ADS)

    Lodders, K.; Fegley, B.

    1993-05-01

    Chemical equilibrium calculations were performed to study the condensation chemistry of the REE and actinides under the highly reducing conditions which are necessary for the formation of the enstatite chondrites. Our calculations confirm that the REE and actinides condensed into oldhamite (CaS), the major REE and actinide host phase in enstatite chondrites, at a carbon-oxygen (C/O) ratio not less than 1 in an otherwise solar gas. Five basic types of REE abundance patterns, several of which are analogous to REE abundance patterns observed in the Ca, Al-rich inclusions in carbonaceous chondrites, are predicted to occur in meteoritic oldhamites. All of the reported REE patterns in oldhamites in enstatite chondrites can be interpreted in terms of our condensation calculations. The observed patterns fall into three of the five predicted categories. The reported Th and U enrichments and ratios in meteoritic oldhamites are also consistent with predictions of the condensation calculations. Pure REE sulfides are predicted to condense in the 10 exp -6 to 10 exp -9 bar range and may be found in enstatite chondrites if they formed in this pressure range.

  12. Innovative Application of Mechanical Activation for Rare Earth Elements Recovering: Process Optimization and Mechanism Exploration

    PubMed Central

    Tan, Quanyin; Deng, Chao; Li, Jinhui

    2016-01-01

    With the rapidly expanding use of fluorescent lamps (FLs) and increasing interest in conservation and sustainable utilization of critical metals such as rare earth elements (REEs), the recovering of REEs from phosphors in waste FLs is becoming a critical environmental and economic issue. To effectively recycle REEs with metallurgical methods, mechanical activation by ball milling was introduced to pretreat the waste phosphors. This current study put the emphasis on the mechanical activation and leaching processes for REEs, and explored the feasibility of the method from both theoretical and practical standpoints. Results showed physicochemical changes of structural destruction and particle size reduction after mechanical activation, leading to the easy dissolution of REEs in the activated samples. Under optimal conditions, dissolution yields of 89.4%, 93.1% and 94.6% for Tb, Eu and Y, respectively, were achieved from activated waste phosphors using hydrochloric acid as the dissolution agent. The shrinking core model proved to be the most applicable for the leaching procedure, with an apparent activation energy of 10.96 ± 2.79 kJ/mol. This novel process indicates that mechanical activation is an efficient method for recovering REEs from waste phosphors, and it has promising potential for REE recovery with low cost and high efficiency. PMID:26819083

  13. High resolution rare-earth elements analyses of natural apatite and its application in geo-sciences: Combined micro-PIXE, quantitative CL spectroscopy and electron spin resonance analyses

    NASA Astrophysics Data System (ADS)

    Habermann, D.; Götte, T.; Meijer, J.; Stephan, A.; Richter, D. K.; Niklas, J. R.

    2000-03-01

    The rare-earth element (REE) distribution in natural apatite is analysed by micro-PIXE, cathodoluminescence (CL) microscopy and spectroscopy and electron spin resonance (ESR) spectroscopy. The micro-PIXE analyses of an apatite crystal from Cerro de Mercado (Mexico) and the summary of 20 analyses of six francolite (conodonts of Triassic age) samples indicate that most of the REEs are enriched in apatite and francolite comparative to average shale standard (NASC). The analyses of fossil francolite revealing the REE-distribution not to be in balance with the REE-distribution of seawater and fish bone debris. Strong inhomogenous lateral REE-distribution in fossil conodont material is shown by CL-mapping and most probably not being a vital effect. Therefore, the resulting REE-signal from fossil francolite is the sum of vital and post-mortem incorporation. The necessary charge compensation for the substitution of divalent Ca by trivalent REE being done by different kind of electron defects and defect ions.

  14. Chemical properties of rare earth elements in typical medical waste incinerator ashes in China.

    PubMed

    Zhao, Lijuan; Zhang, Fu-Shen; Zhang, Jingxin

    2008-10-30

    Medical waste (MW) ashes from different types of MW incinerators were examined to detect the characteristics and environmental impact of rare earth elements (REEs). The results showed that total REE contents in the ash samples ranged from 10.2 to 78.9 mg/kg. REEs in bottom ash were apparently higher than those in fly ash. Average REE contents in the ashes followed the sequence of Ce>La>Nd>Y>Gd>Pr>Sm>Dy>Er>Yb>Ho>Eu>Tb>Lu>Tm. Some of the elements, such as Sm, Dy, Ho, Er, Yb in the ash samples were in normal or nearly normal distribution, but Y, La, Ce, Pr, Nd, Eu, Gd, Tb, Tm, Lu were not normally distributed, indicating some of the ash samples were enriched with these elements. Crust-normalized REE patterns indicated that two types of the MW ashes were obviously enriched with Gd and La. Sequential extraction results showed that REEs in the ash mainly presented as residual fraction, while exchangeable and carbonate fractions were relatively low. DTPA- and EDTA-extraction tests indicated that REEs in the MW ashes were generally in low bioavailability. PMID:18329796

  15. PPI-responsive esophageal eosinophilia and eosinophilic esophagitis: More similarities than differences

    PubMed Central

    Eluri, Swathi; Dellon, Evan S.

    2015-01-01

    Purpose of review To discuss the clinical, endoscopic, and histologic features, pathogenesis, and disease mechanisms of proton pump inhibitor–responsive esophageal eosinophilia (PPI-REE), and to highlight similarities and differences with eosinophilic esophagitis (EoE). Recent findings PPI-REE is a condition in which patients have clinical and histologic findings similar to EoE, but achieve complete remission with proton pump inhibitor (PPI) treatment. More than one-third of patients who have esophageal symptoms associated with esophageal eosinophilia respond to PPI treatment. Emerging data elucidating the pathogenesis of PPI-REE have shown that Th2-related inflammatory factors such as IL-13, IL-5, eotaxin-3, and major basic protein (MBP) are elevated in PPI-REE, similar to EoE. PPI-REE also shares a genetic expression signature with EoE that reverses with PPI treatment. Mechanisms proposed to explain the PPI response include an acid-independent, anti-inflammatory action of PPIs and PPI-induced restoration of esophageal barrier function. Summary Multiple features of PPI-REE overlap extensively with EoE. This raises the question of whether PPI-REE is merely a subtype of EoE rather than an independent condition. This similarity may have future implications for algorithms informing evaluation and treatment of esophageal eosinophilia. PMID:26039722

  16. Lanthanide and actinide chemistry at high C/O ratios in the solar nebula

    NASA Technical Reports Server (NTRS)

    Lodders, Katharina; Fegley, Bruce, Jr.

    1993-01-01

    Chemical equilibrium calculations were performed to study the condensation chemistry of the REE and actinides under the highly reducing conditions which are necessary for the formation of the enstatite chondrites. Our calculations confirm that the REE and actinides condensed into oldhamite (CaS), the major REE and actinide host phase in enstatite chondrites, at a carbon-oxygen (C/O) ratio not less than 1 in an otherwise solar gas. Five basic types of REE abundance patterns, several of which are analogous to REE abundance patterns observed in the Ca, Al-rich inclusions in carbonaceous chondrites, are predicted to occur in meteoritic oldhamites. All of the reported REE patterns in oldhamites in enstatite chondrites can be interpreted in terms of our condensation calculations. The observed patterns fall into three of the five predicted categories. The reported Th and U enrichments and ratios in meteoritic oldhamites are also consistent with predictions of the condensation calculations. Pure REE sulfides are predicted to condense in the 10 exp -6 to 10 exp -9 bar range and may be found in enstatite chondrites if they formed in this pressure range.

  17. Interoceanic variation in the rare earth, major, and trace element depositional chemistry of chert: Perspectives gained from the DSDP and ODP record

    SciTech Connect

    Murray, R.W.; Jones, D.L. ); Buchholtz Ten Brink, M.R.; Gerlach, D.C.; Russ, G.P. III )

    1992-05-01

    Rare earth element (REE), major, and trace element abundances and relative fractionations in forty nodular cherts sampled by the Deep Sea Drilling Project (DSDP) and Ocean Drilling Program (ODP) indicate that the REE composition of chert records the interplay between terrigenous sources and scavenging from the local seawater. Chert from the large Pacific Ocean, where deposition occurs relatively removed from significant terrigenous input, records a depositional REE signal dominated by adsorption of dissolved REEs from sea water. Chert from the Atlantic basin, a moderately sized ocean basin lined by passive margins and with more terrigenous input than the Pacific, records a mix of adsorptive and terrigenous REE signals, with moderately negative Ce anomalies and La{sub n}/YB{sub n} ratios intermediate to those of the Pacific and those of terrigenous input. Chert from the southern high latitude region is dominated by the large terrigenous input on the Antarctic passive margin, with inherited Ce/Ce{sup *} {approximately} 1 and inherited La{sub n}/Yb{sub n} values of {approximately} 1.2-1.4. This and previous studies of the large-scale controlling parameters of sedimentary REEs across ocean basins collectively indicate that REE indices of depositional regime (e.g., Ce/Ce{sup *}, La{sub n}/Yb{sub n}, La{sub ex}) are reproducible in a variety of sediment and rock lithologies, ages, and ocean basins, and present a coherent tool for paleoceanographic and tectonic basin reconstructions.

  18. Determination of rare earth elements in environmental materials by inductively coupled plasma mass spectrometry

    SciTech Connect

    Panday, V.K.; Hoppstock, K.; Becker, J.S.; Dietze, H.J.

    1996-09-01

    Despite the fact that rare earth elements (REE) have found increasing use in modern technology only few data are available on their concentrations in biological and environmental samples. Inductively coupled plasma mass spectrometry (ICP-MS) has been employed to study the concentration of rare earth elements (REE) in various environmental materials (e.g., pine needles, mussel tissue, apple leaves) available from National Institute of Standards and Technology (NIST), the Bureau of European Communities (BCR), and the German Environmental Specimens Bank. After the decomposition of the environmental samples with HNO{sub 3}, the REE (present mostly in the ng/g-range) were separated from the matrix and simultaneously preconcentrated using liquid-liquid extraction with bis(2-ethyl hexyl)-ortho-phosphoric acid (HDEHP) in toluene as a selective reagent at pH = 2 and subsequent back extraction of the elements into the aqueous by 6M HNO{sub 3}. Recoveries of better 90% were obtained for almost all REE. A Perkin Elmer/Sciex ELAN 5000 ICP-MS and HR-ICP-MS ELEMENT from Finnigan MAT were used for quantitative analysis (by external calibration and ID-ICP-MS) of REE. The results of determination of REE concentrations agree well with the data available on some of these materials. Further supplement information on the contents of various REE in these materials.

  19. Atmospheric deposition of rare earth elements in Albania studied by the moss biomonitoring technique, neutron activation analysis and GIS technology.

    PubMed

    Allajbeu, Sh; Yushin, N S; Qarri, F; Duliu, O G; Lazo, P; Frontasyeva, M V

    2016-07-01

    Rare earth elements (REEs) are typically conservative elements that are scarcely derived from anthropogenic sources. The mobilization of REEs in the environment requires the monitoring of these elements in environmental matrices, in which they are present at trace level. The determination of 11 REEs in carpet-forming moss species (Hypnum cupressiforme) collected from 44 sampling sites over the whole territory of the country were done by using epithermal neutron activation analysis (ENAA) at IBR-2 fast pulsed reactor in Dubna. This paper is focused on REEs (lanthanides) and Sc. Fe as typical consistent element and Th that appeared good correlations between the elements of lanthanides are included in this paper. Th, Sc, and REEs were never previously determined in the air deposition of Albania. Descriptive statistics were used for data treatment using MINITAB 17 software package. The median values of the elements under investigation were compared with those of the neighboring countries such as Bulgaria, Macedonia, Romania, and Serbia, as well as Norway which is selected as a clean area. Geographical distribution maps of the elements over the sampled territory were constructed using geographic information system (GIS) technology. Geochemical behavior of REEs in moss samples has been studied by using the ternary diagram of Sc-La-Th, Spider diagrams and multivariate analysis. It was revealed that the accumulation of REEs in current mosses is associated with the wind-blowing metal-enriched soils that is pointed out as the main emitting factor of the elements under investigation. PMID:27044293

  20. High-resolution and high-sensitivity tephra-inferred fingerprints in stalagmite geochemistry

    NASA Astrophysics Data System (ADS)

    Wu, Chung-Che; Burger, Marcel; Günther, Detlef; Hattendorf, Bodo; Shen, Chuan-Chou

    2016-04-01

    High-resolution and high-sensitivity rare earth elements (REEs) profiles of Holocene stalagmites collected from East Timor (8° 47' S, 126° 23' E) provide detailed fluctuation information which can be inferred to super volcano eruptions. Since REEs are enriched in igneous rocks (~ μg/g) but depleted in carbonates (~ ng/g to pg/g), REEs preserved in stalagmites are acted as an ideal proxy of tephra-inferred signature; however, due to the low REE abundances in most natural stalagmite samples (1-100s ng/g), overall applicability has been sharply limited. Here we develop and apply an improved LA-GED-ICPMS methodology to determine REEs in such low concentration stalagmites. Two pronounced REE peaks occur where their concentrations sharply increased by 1-2 order of magnitudes, from 10s of ng/g to 100s of ng/g. This event was dated at 80 thousand years ago by U-Th methods. Nevertheless, the accurate timing of this REE anomalous event should be examined carefully. Also more multi-proxies evidences such as stable isotopes δ13C, δ18O, and S isotope, should be provided in the future.

  1. Preliminary estimates of the quantities of rare-earth elements contained in selected products and in imports of semimanufactured products to the United States, 2010

    USGS Publications Warehouse

    Bleiwas, Donald I.; Gambogi, Joseph

    2013-01-01

    Rare-earth elements (REEs) are contained in a wide range of products of economic and strategic importance to the Nation. The REEs may or may not represent a significant component of that product by mass, value, or volume; however, in many cases, the embedded REEs are critical for the device’s function. Domestic sources of primary supply and the manufacturing facilities to produce products are inadequate to meet U.S. requirements; therefore, a significant percentage of the supply of REEs and the products that contain them are imported to the United States. In 2011, mines in China produced roughly 97 percent of the world’s supply of REEs, and the country’s production of these elements will likely dominate global supply until at least 2020. Preliminary estimates of the types and amount of rare-earth elements, reported as oxides, in semimanufactured form and the amounts used for electric vehicle batteries, catalytic converters, computers, and other applications were developed to provide a perspective on the Nation’s use of these elements. The amount of rare-earth metals recovered from recycling, remanufacturing, and reuse is negligible when the tonnage of products that contain REEs deposited in landfills and retained in storage is considered. Under favorable market conditions, the recovery of REEs from obsolete products could potentially displace a portion of the supply from primary sources.

  2. Effect of earthworms (Eisenia fetida) on the fractionation and bioavailability of rare earth elements in nine Chinese soils.

    PubMed

    Wen, Bei; Liu, Ying; Hu, Xiao-yu; Shan, Xiao-quan

    2006-05-01

    The effect of earthworm (Eisenia fetida) activity on soil pH, dissolved organic carbon (DOC), fraction distribution pattern and bioavailability of rare earth elements (REEs) Y, La, Ce, Pr and Nd in nine Chinese soils were investigated using pot experiments. A three-step extraction procedure recommended by the European Community (Standards, Measurements and Testing Programme) was used to fractionate REEs in soils into water soluble, exchangeable and carbonate bound (B1), Fe- and Mn-oxides bound (B2) and organic matter and sulfide bound (B3). Inoculated with earthworms, the soil pH, DOC and water-soluble rare earth elements fraction increased. A significant correlation was obtained between the increased DOC and the increased water-soluble REEs. REEs in fraction B1 increased after earthworm inoculation, while those in fraction B3 decreased. No significant differences were observed for REEs in fraction B2. The biomass and the concentrations of REEs in wheat shoots and roots increased after the treatment with earthworms. The results demonstrated that earthworm activity increased the mobility and bioavailability of REEs in soils. PMID:16289225

  3. Size distribution of rare earth elements in coal ash

    USGS Publications Warehouse

    Scott, Clinton T.; Deonarine, Amrika; Kolker, Allan; Adams, Monique; Holland, James F.

    2015-01-01

    Rare earth elements (REEs) are utilized in various applications that are vital to the automotive, petrochemical, medical, and information technology industries. As world demand for REEs increases, critical shortages are expected. Due to the retention of REEs during coal combustion, coal fly ash is increasingly considered a potential resource. Previous studies have demonstrated that coal fly ash is variably enriched in REEs relative to feed coal (e.g, Seredin and Dai, 2012) and that enrichment increases with decreasing size fractions (Blissett et al., 2014). In order to further explore the REE resource potential of coal ash, and determine the partitioning behavior of REE as a function of grain size, we studied whole coal and fly ash size-fractions collected from three U.S commercial-scale coal-fired generating stations burning Appalachian or Powder River Basin coal. Whole fly ash was separated into , 5 um, to 5 to 10 um and 10 to 100 um particle size fractions by mechanical shaking using trace-metal clean procedures. In these samples REE enrichments in whole fly ash ranges 5.6 to 18.5 times that of feedcoals. Partitioning results for size separates relative to whole coal and whole fly ash will also be reported. 

  4. Rare earth elements in Hamersley BIF minerals

    NASA Astrophysics Data System (ADS)

    Alibert, Chantal

    2016-07-01

    Minerals from the Hamersley banded iron formation, Western Australia, were analyzed for Y and rare earth elements (YREEs) by laser ablation ICP-MS to investigate diagenetic pathways, from precursor phases to BIF minerals. One group of apatites carries the seawater REE signature, giving evidence that P and REEs, thoroughly scavenged from the water column by Si-ferrihydrite particles, were released upon microbial Fe3+ reductive dissolution of Si-ferrihydrite in pore-water and finally sequestered mainly in authigenic apatite. The absence of fractionation between apatite and seawater suggests that REE were first incorporated into an amorphous calcium phosphate as fully hydrated cations, i.e. as outer-sphere complexes. The iron oxides and carbonates carry only a small fraction of the whole-rock REE budget. Their REE patterns are distinctly enriched in Yb and show some M-type tetrad effect consistent with experimental Kd(REE) between solid and saline solution with low carbonate ion concentrations. It is deduced that hematite formed at an incipient stage of Fe2+-catalyzed dissolution of Si-ferrihydrite, via a dissolution-reprecipitation pathway. The REE pattern of greenalite, found as sub-micron particles in quartz in a chert-siderite sample, is consistent with its authigenic origin by precipitation in pore-water after dissolution of a small amount of Si-ferrihydrite. Magnetite carries very low YREEs (ppb-level), has an homogeneous pattern distinctly enriched in the mid-REEs compared to hematite, and includes a late population depleted in light-REEs, Ba and As. Magnetite forming aggregates and massive laminae is tentatively interpreted as reflecting some fluid-aided hematite-magnetite re-equilibration or transformation at low-grade metamorphic temperatures.

  5. The surface sediment types and their rare earth element characteristics from the continental shelf of the northern south China sea

    NASA Astrophysics Data System (ADS)

    Wang, Shuhong; Zhang, Nan; Chen, Han; Li, Liang; Yan, Wen

    2014-10-01

    The grain size as well as some major and trace elements, including rare earth element (REE), for 273 surface sediment samples collected from the continental shelf of the northern South China Sea were analyzed in this study. The sediment types are mainly sandy silt and silt, making up 60% of the whole samples, and secondly are mud, sandy mud, muddy sand and silty sand, making up 28% of the whole samples, based on grain-size in which the Folk's classification was used. The total REE content (ΣREE) show a wide variation from 21 ppm to 244 ppm with an average value of 155 ppm, which similar to the average ΣREE of the China loess, but much different from that in deep-sea clay, showing a significant terrigenous succession. The REE contents in different sediment types vary greatly, mainly enriching in silt, sandy silt, mud and sandy mud. The REE distribution contours parallel to the coastal, presenting like strips and their contents gradually reduce with increasing distance from the coast. The high content of the western Pearl River Mouth, Shang/Xiachuan Islands and Hailing Bay might be regarded to the coastal current developed from the east to the west along to the Pearl River Mouth in the northern South China Sea. But the chondrite-normalized REE patterns in various sediment types have no difference, basically same as those of coastal rivers and upper crust. They all show relative enrichments in light rare earth element (LREE), noticeable negative Eu anomaly and no Ce anomaly, indicating that those sediments are terrigenous sediments and from the same source region. Further analysis suggest that the sedimentary environment in the study area is relatively stable and granite widely distributed in the South China mainland is the main source of REE, which are transported mainly by the Pearl River. The late diagenesis has little effect on the REE.

  6. Biogeochemical implications from dissolved rare earth element and Nd isotope distributions in the Gulf of Alaska

    NASA Astrophysics Data System (ADS)

    Haley, Brian A.; Frank, Martin; Hathorne, Ed; Pisias, Nick

    2014-02-01

    Dissolved rare earth element (REE) concentrations and Nd isotope compositions were measured for surface waters and full water column profiles of the Gulf of Alaska (GoA), and compared to water mass properties and circulation in order to better understand the mechanisms controlling the input and transport of REEs in the ocean. The REEs display a typical open-ocean range of concentrations (i.e., La: 12-66 pM; Lu: 0.2-2.5 pM) and depth distributions (i.e., surface ocean depletion and enrichment with water depth). Nd isotope signatures are highly radiogenic, as expected for the North Pacific margin (ranging from -3.8 to +0.2 ɛNd). The most radiogenic values were found in the coastal waters but also in the cores of eddies, indicating efficient export of REEs from the margins and across the mixed layer. This is the first time that distinct Nd isotope distributions in near surface waters can be directly assigned to offshore eddy transport. A distinct mid-depth (˜2200 m) Nd isotope signal was found that most likely reflects advection of a water mass that formed through past down-welling in the Northern Pacific. Subsurface Nd isotope compositions appear to behave conservatively and can be explained through a REE distribution model proposed here. This model is based on multivariate analysis of the REEs and invokes two distinct “pools” of dissolved REEs: a “passive pool” complexed by carbonate ions, and a “bio-reactive pool” that is microbially manipulated. The latter “pool” is only significant in the upper water column and most likely reflects the indirect effects of microbial cycling of iron. Our model of the open ocean REE distribution contributes to explaining the conservative nature of Nd isotopes and provides a mechanism linking surface ocean and pore water REE dynamics.

  7. The relationship between resting energy expenditure and weight loss in benign and malignant disease.

    PubMed Central

    Hansell, D T; Davies, J W; Burns, H J

    1986-01-01

    The relationship between cancer, weight loss, and resting energy expenditure (REE) has been investigated in 136 patients using indirect calorimetry. Ninety-one patients had gastric, colorectal, or nonsmall cell bronchial neoplasm, seven patients had other malignancies, and 38 patients had nonmalignant illness. Four groups were studied: weight stable cancer patients (CWS: N = 56), weight losing cancer patients (CWL: N = 42), weight stable patients with nonmalignant illness (NCWS: N = 22), and weight losing patients with nonmalignant illness (NCWL: N = 16). In each group REE correlated significantly with body weight, metabolic body size, and lean body mass (LBM: estimated from total body water measurements). The closest correlation was between REE and lean body mass, with the slope of the CWL regression line differing significantly from that of the CWS (p less than 0.05) and NCWS (p less than 0.02) groups. However, there was no difference in REE expressed as kcal/kg LBM/d between the groups. The slopes of the regressions between REE and LBM were almost identical when all cancer patients were compared with all patients with nonmalignant illness. However, when all weight stable patients were compared with all weight losing patients, there was a highly significant difference between the slopes of the regressions (p less than 0.005). This indicates that the weight losing state rather than the presence or absence of cancer is responsible for an alteration in the relationship between REE and LBM. There were no differences in REE between the different tumor types. It is concluded that REE is not elevated in patients with gastric, colorectal, or nonsmall cell bronchial cancer. Elevation of REE contributes very little to the etiology of cancer cachexia. PMID:3082302

  8. Rare earth element content in various waste ashes and the potential risk to Japanese soils.

    PubMed

    Zhang, F S; Yamasaki, S; Kimura, K

    2001-11-01

    Selected chemical characteristics of rare earth elements (REEs) in 89 waste ash samples, including food scrap ashes (FSA), animal waste ashes (AWA), horticulture waste ashes (HWA), sewage sludge ashes (SSA) and incinerator bottom ashes (IBA), were examined in this study. The results showed that Y, La, Ce, Pr, Nd, Dy, Yb, Ho, Er, Tm, Lu in the waste ash samples were normally distributed, but Sc, Sm, Eu, Gd, Tb were not. Average REE concentrations followed the sequence of Ce > La = Y> Sc>Nd>Sm>Pr>Gd>Dy>Eu>Tb>Er> Yb>Ho>Lu>Tm. Of the five types of waste ashes, total REE contents (sigmaREE) ranged from 54 to 130 mg/kg, following the sequence of SSA>HWA>IBA>AWA>FSA; individual REE concentrations were within 0.04-20, 0.1-29, 0.2-33, 0.1-44 and 0.01-41 mg/kg for FSA, AWA, HWA, SSA and IBA, respectively. Crust-normalized REE patterns indicated that SSA was enriched with Sc, Sm, Eu, Gd, Tb and slightly enriched with La, Ce; IBA was enriched with Eu, Tb and slightly with La, Y, Ce; FSA was slightly enriched with Sm, Eu, Tb; REEs were not found to be elevated in HWA and AWA. Comparison of REE content in the waste ashes and in six principal Japanese agricultural soils indicated that application of FSA, AWA and HWA to agricultural land will cause no REE problem, but continuous application of SSA or IBA may cause Sc, Sm or Eu accumulation in some of the soils. PMID:11757853

  9. Isotopic and chemical systematics of river waters

    SciTech Connect

    Goldstein, S.J.

    1987-01-01

    The isotopic composition of Nd and Sr and the concentration of the rare earth elements (REE), Rb, and Sr are reported for the dissolved and suspended load of rivers from North America, Australia, Japan, the Philippines, South America, and Pakistan. Nd and light REE are mobilized in solution in rivers of low pH, whereas Sr concentrations are generally determined by the degree of chemical weathering of source rocks. The REE pattern of the dissolved load of rivers is sensitive to pH, with heavy REE enrichments and negative Ce anomalies for alkaline rivers. The isotopic composition of Nd and Sr in the dissolved load of rivers is mainly controlled by the age of materials in a drainage basin and preferential weathering of marine precipitates. Rivers appear to be the dominant source of these elements in the oceans. Estuarine removal processes lower the actual river flux of dissolved REE to the oceans by 70% for the light REE and 40% for the heavy REE. A Sr isotopic mass balance for modern seawater yields a hydrothermal water of 2.9 x 10/sup 16/ g/yr. Suspended load data directly reflect the Sm-Nd isotopic systematics and REE systematics of upper continental crust exposed to weathering. Average Sm-Nd parameters estimated for the upper crust are: Sm = 5.7 ppm. Nd = 30.0 ppm, epsilon/sub Nd/ = -15.4, and T/sub DM//sup Nd/ = 2.0 Ga. An overall relationship between epsilon/sub Nd/ and /sup 87/Sr//sup 86/Sr in river suspended loads directly reflects the relationship of these parameters in upper crust and suggests that crustal additions have become progressively depleted in incompatible elements through time. The implications of these data for interpretation of the record of Nd and Sr isotopes and REE abundances in ancient erosion products are briefly discussed.

  10. Rare earth elements in synthetic zircon. 2. a single-crystal x-ray study of xenotime substitution.

    SciTech Connect

    Finch, R. J.; Hanchar, J. M.; Hoskin, P. W. O.; Burns, P. C.; Chemical Engineering; Australian National Univ.; Univ. of Notre Dame

    2001-05-01

    Zircon crystals synthesized in a Li-Mo oxide melt and doped with trivalent lanthanides and Y (REE), both with and without P, were examined by single-crystal X-ray diffraction (XRD). REE are incorporated into the Zr site in the zircon structure, and some Zr appears to be displaced to the Si site. Crystals doped with middle REE (MREE, Sm to Dy) and Y, plus P follow the xenotime substitution (REE{sup 3+} + P{sup 5+} = Zr{sup 4+} + Si{sup 4+}) rather closely, whereas crystals doped with heavy REE (HREE, Er to Lu) deviate from the xenotime substitution, having REE:P atomic ratios significantly greater than one. Xenotime substitution requires that P{sup 5+} replace Si{sup 4+}, but this substitution becomes limited by strain at the Si site in HREE-doped crystals. As Si sites become saturated with P{sup 5+}, additional charge balance in synthetic zircon crystals may be provided by Mo{sup 6+} and Li{sup +} from the flux entering interstitial sites, accounting for an additional 0.3 to 0.6 at% HREE beyond that balanced by P{sup 5+} ions. Heavy REE are more compatible in the zircon structure than are LREE and MREE, and HREE substitution is ultimately limited by the inability of the zircon structure to further accommodate charge-compensating elements. Thus the limit on REE concentrations in zircon is not a simple function of REE{sup 3+} ionic radii but depends in a complex way on structural strain at Zr and Si sites, which act together to limit REE and P incorporation. The mechanisms that limit the coupled xenotime substitution change from LREE to HREE. This change means that REE fractionation in zircon may vary according to the availability of charge-compensating elements. REE partition coefficients between zircon and melt must also depend in part on the availability of charge-compensating elements and their compatibility in the zircon structure.

  11. The adsorption of rare earth ions using carbonized polydopamine nano shells

    DOE PAGESBeta

    Sun, Xiaoqi; Luo, Huimin; Mahurin, Shannon Mark; Dai, Sheng; Liu, Rui; Hou, Xisen; Dai, Sheng

    2016-01-07

    Herein we report the structure effects of nano carbon shells prepared by carbonized polydopamine for rare earth elements (REEs) adsorption for the first time. The solid carbon sphere, 60 nm carbon shell and 500 nm carbon shell were prepared and investigated for adsorption and desorption of REEs. The adsorption of carbon shells for REEs was found to be better than the solid carbon sphere. The effect of acidities on the adsorption and desorption properties was discussed in this study. The good adsorption performance of carbon shells can be attributed to their porous structure, large specific surface area, amine group andmore » carbonyl group of dopamine.« less

  12. Rare Earth Elements: A Tool for Understanding the Behaviour of Trivalent Actinides in the Geosphere

    SciTech Connect

    Buil, Belen; Gomez, Paloma; Garralon, Antonio; Turrero, M. Jesus

    2007-07-01

    Rare earth element (REE) concentrations have been determined in groundwaters, granite and fracture fillings in a restored uranium mine. The granitoids normalized REE patterns of groundwaters show heavy rare earth elements (HREE)-enrichment and positive Eu anomalies. This suggests that the REE are fractionated during leaching from the source rocks by groundwaters. Preferential leaching of HREE would be consistent with the greater stability of their aqueous complexes compared to those of the light rare earth elements (LREE), together with the dissolution of certain fracture filling minerals, dissolution/alteration of phyllosilicates and colloidal transport. (authors)

  13. Excess europium content in Precambrian sedimentary rocks and continental evolution

    NASA Technical Reports Server (NTRS)

    Jakes, P.; Taylor, S. R.

    1974-01-01

    It is proposed that the europium excess in Precambrian sedimentary rocks, relative to those of younger age, is derived from volcanic rocks of ancient island arcs, which were the source materials for the sediments. Precambrian sedimentary rocks and present-day volcanic rocks of island arcs have similar REE patterns, total REE abundances, and excess Eu, relative to the North American shale composite. The present upper crustal REE pattern, as exemplified by that of sediments, is depleted in Eu, relative to chondrites. This depletion is considered to be a consequence of development of a granodioritic upper crust by partial melting in the lower crust, which selectively retains europium.

  14. Trace-element abundances in several new ureilites

    NASA Technical Reports Server (NTRS)

    Boynton, William V.; Hill, Dolores H.

    1993-01-01

    Four new ureilites are analyzed for trace-element abundances. Frontier Mountain (FRO) 90054 is an augite-rich ureilite and has high rare earth element (REE) abundances with a pattern expected of augite. FRO 90036 and Acfer 277 have REE patterns similar to the V-shape pattern of other ureilites. Nuevo Mercurio (b) has very high REE abundances, but they look like they are due to terrestrial alteration. The siderophile-element pattern of these ureilites are similar to those of known ureilites.

  15. Renormalized entanglement entropy flow in mass-deformed ABJM theory

    NASA Astrophysics Data System (ADS)

    Kim, Kyung Kiu; Kwon, O.-Kab; Park, Chanyong; Shin, Hyeonjoon

    2014-08-01

    We investigate a mass deformation effect on the renormalized entanglement entropy (REE) near the UV fixed point in (2+1)-dimensional field theory. In the context of the gauge/gravity duality, we use the Lin-Lunin-Maldacena geometries corresponding to the vacua of the mass-deformed ABJM theory. We analytically compute the small mass effect for various droplet configurations and show in holographic point of view that the REE is monotonically decreasing, positive, and stationary at the UV fixed point. These properties of the REE in (2+1)-dimensions are consistent with the Zamolodchikov c-function proposed in (1+1)-dimensional conformal field theory.

  16. Comparison of microconcentric and membrane-desolvation sample introduction systems for determination of low rare earth element concentrations in surface and subsurface waters using sector field inductively coupled plasma mass spectrometry

    NASA Astrophysics Data System (ADS)

    Chung, Chuan-Hsiung; Brenner, Isaac; You, Chen-Feng

    2009-09-01

    Analytical performances of a microconcentric nebulizer (MCN) and a membrane-desolvation sample introduction system (Aridus) were compared for determination of low concentrations of rare earth elements (REEs) in surface and subsurface waters using a double focusing sector field inductively coupled plasma mass spectrometer. Conventional figures of merit were employed, such as sensitivities, limits of detection (LOD), REE-O + formation, matrix induced interferences, long term signal variations, and recovery from spiked sea water samples and a pristine water CRM. Sensitivity as a function of mass for the MCN was quite flat with the exception of light REE (LREE +) which was dependent on REE-O + generation. Signal responses using the Aridus were enhanced by factors of 4-10. Large sensitivity enhancements were observed for 139La +, 140Ce + and 141Pr +, due to the attenuation of their REE-O + (where the Aridus 140Ce 16O +/ 140Ce + was three orders of magnitude lower than that determined using the MCN) as a result of water analysis reduction in the plasma. Despite higher sensitivities, Aridus LODs were not significantly different from those obtained using the MCN, and values varied from 0.05 to 0.2 ng L - 1 and 0.1 to 0.2 ng L - 1 for the MCN and Aridus systems, respectively. When using the MCN, LREE + signals were closely associated with REE-O bond strengths, implying that LREE-O + production and breakdown are related to the strength of REE-O bonds in REE-O + ions suggesting that medium REE (MREE)-O + and heavy REE (HREE)-O + if formed, were thermally unstable in the plasma. In the presence of conservative Na concentrations, MCN LREE + signal suppressions varied from about 15 to 25% and about 5 to 10% for MREE + and HREE +. In contrast, regular 15% signal suppressions for all REE + were observed for the Aridus. In the case of the MCN, more than one internal standard is required for compensation for these different effects, whereas a single internal standard ( 159Tb

  17. Miocene Coral Skeleton Rare Earth Element Patterns Reflect River Discharge

    NASA Astrophysics Data System (ADS)

    Mertz-Kraus, R.; Brachert, T. C.; Jochum, K. P.

    2010-12-01

    Rare Earth Element (REE) patterns of modern coral skeletons usually reflect the REE composition of ambient seawater which is characterized by heavy REE enriched relative to light REE with NASC (North American Shale Composite) normalized La/Lu ratios of typically <0.4. The REE concentration in coral aragonite is enriched by 3 to 4 orders of magnitude compared to ambient seawater. Here we report trace element data including REE of coral skeletons of Late Miocene age (~9 Ma, Tortonian) from Crete (Eastern Mediterranean). Analyses were done using a 213 nm Nd:YAG laser coupled to an Element2 ICP-MS along the growth axis of the coral skeletons. The profiles show that Ba/Ca ratios have a seasonally induced pattern with high values around the winter months which are identified by δ18O analyses. REE/Ca ratios co-vary with Ba/Ca ratios. Since the Ba/Ca ratio is a proxy used to monitor river discharge, the co-variation suggests the REE/Ca ratio to be a proxy of comparable quality. NASC-normalized REE patterns of the Tortonian corals have negative Ce anomalies like modern corals. However, the Tortonian corals have REE patterns highly enriched in LREE with (La/Lu)N ratios of 4 to 30 which is 1 to 2 orders of magnitude higher compared to modern corals. Al concentrations are low (<10 ppm) and do not correlate with REE concentrations indicating an insignificant fraction of terrigenous material included in the skeleton. Applying distribution coefficients typical for modern corals, the REE composition of the Tortonian ambient water yields (La/Lu)N of about 2 to 16. This range can be explained by binary mixing of modern Eastern Mediterranean sea surface water ((La/Lu)N=0.35, sea surface salinity (SSS) ~38 ‰) with highly LREE-enriched river water ((La/Lu)N >3, salinity ~0.5 ‰) transporting suspended and colloid phases, also highly enriched, especially in LREE, at a ratio of ~9 (seawater):1 (river water). The river water component is considered because paleoenvironmental

  18. Comparative studies on the concentration of rare earth elements and heavy metals in the atmospheric particulate matter in Beijing, China, and in Delft, The Netherlands.

    PubMed

    Wang, C X; Zhu, W; Peng, A; Guichreit, R

    2001-05-01

    Atmospheric particulate matter (APM) was collected at three sampling sites in Beijing, China, from February to June 1998. The concentrations of rare earth elements (REE) and cobalt (Co), zinc (Zn), copper (Cu), cadmium (Cd) and lead (Pb) in the APM were determined by inductively coupled plasma mass spectrometry (ICP-MS). The results obtained in Beijing, China, were compared to that obtained in Delft, the Netherlands, in 1997. The influence of coal combustion was considered. The results demonstrated that the content of APM, the concentrations of REE and Co, Zn, Cd, Pb in the APM in Beijing, China, were higher than that in Delft, the Netherlands. From the ratios of La to Ce, and La to Sm, which may be used as tracers for the origin of the REE, it is concluded that the origins of REE in China differ from those in the Netherlands. PMID:11392744

  19. Rare Earth Element Complementarity in CO and CV Chondrites

    NASA Astrophysics Data System (ADS)

    Crapster-Pregont, E. J.; Friedrich, J. M.; Ebel, D. S.

    2014-09-01

    LREE/HREE ratios in each component of CO and CV chondrites combine to produce complementary, flat bulk REE pattern, while individually yielding insight into mineral controls and precursor characteristics.

  20. Petrography and bulk chemistry of Martian orthopyroxenite ALH84001: implications for the origin of secondary carbonates.

    PubMed

    Gleason, J D; Kring, D A; Hill, D H; Boynton, W V

    1997-08-01

    New petrologic and bulk geochemical data for the SNC-related (Martian) meteorite ALH84001 suggest a relatively simple igneous history overprinted by complex shock and hydrothermal processes. ALH84001 is an igneous orthopyroxene cumulate containing penetrative shock deformation textures and a few percent secondary extraterrestrial carbonates. Rare earth element (REE) patterns for several splits of the meteorite reveal substantial heterogeneity in REE abundances and significant fractionation of the REEs between crushed and uncrushed domains within the meteorite. Complex zoning in carbonates indicates nonequilibrium processes were involved in their formation, suggesting that CO2-rich fluids of variable composition infiltrated the rock while on Mars. We interpret petrographic textures to be consistent with an inorganic origin for the carbonate involving dissolution-replacement reactions between CO2-charged fluids and feldspathic glass in the meteorite. Carbonate formation clearly postdated processes that last redistributed the REE in the meteorite. PMID:11540477

  1. Rare earth elements in minerals of the ALHA77005 shergottite and implications for its parent magma and crystallization history

    NASA Technical Reports Server (NTRS)

    Lundberg, Laura L.; Crozaz, Ghislaine; Mcsween, Harry Y., Jr.

    1990-01-01

    Analyses of mineral REE and selected minor and trace elements were carried out on individual grains of pyroxenes, whitlockite, maskelynite, and olivine of the Antarctic shergottite ALHA77005, and the results are used to interpret its parent magma and crystallization history. The results of mineral compositions and textural observations suggest that ALHA77005 is a cumulate with about half cumulus material (olivine + chromite) and half postcumulus phases. Most of the REEs in ALHA77005 reside in whitlockite whose modal concentration is about 1 percent. Mineral REE data support previous suggestions that plagioclase and whitlockite crystallized late, and that low-Ca pyroxene initiated crystallization before high-Ca pyroxene. The REE patterns for the intercumulus liquid, calculated from distribution coefficients for ALHA77005 pyroxene, plagioclase, and whitlockite, are in very good agreement and are similar to that of Shergotty.

  2. Sm-Nd systematics of a tonalitic augen gneiss and its constituent minerals from northern Michigan

    USGS Publications Warehouse

    Futa, K.

    1981-01-01

    The Sm-Nd isotopic system of a tonalitic augen gneiss and its constituent minerals from northern Michigan was disturbed during metamorphism. Sm-Nd zircon ages are lower than the wholerock Sm-Nd model age. However, closely associated pairs of minerals (for example, sphene and biotite or apatite and plagioclase) retain their apparent metamorphic ages. The Sm-Nd model age for the tonalitic augen gneiss of 3919 ?? 30myr, appears to reflect open system behavior during metamorphism. A mineralogically different gneiss from the same location has a Sm-Nd model age of 3520 ?? 70 myr. The two whole rocks differ in their Sm-Nd and Rb-Sr systematics and in their chondrite-normalized rare earth element (REE) patterns. The whole-rock-normalized mineral REE patterns show the contribution of the major and trace minerals to the REE content of the whole rock. The trace minerals contain a significant amount of the total REE. ?? 1981.

  3. Cerium chloride heptahydrate (CeCl3 · 7H2O) induces muscle paralysis in the generalist herbivore, Melanoplus sanguinipes (Fabricius) (Orthoptera: Acrididae), fed contaminated plant tissues.

    PubMed

    Allison, Jane E; Boutin, Céline; Carpenter, David; Ellis, Deanna M; Parsons, Jessica L

    2015-02-01

    Of increasing economic importance are the rare earth elements (REEs). Pollution from mining and processing activity is expected to rise with industrial demand. Plants are known to accumulate REEs, although levels vary with species and soil content. However, the effect on wildlife of ingesting REE contaminated vegetation is not well understood. Here we examined the effect of consuming vegetation with elevated levels of cerium on the generalist grasshopper, Melanoplus sanguinipes (Fabricius). Adults excreted a substantial portion of ingested contamination. However, after only four-days of feeding, accumulation in the body occurred at all doses and paralysis of appendages resulted at the highest doses. Short-term toxicity studies may underestimate the impact of ingesting REE contamination. Metals tend to be low in toxicity; however, their persistence in the environment may be better represented by exposure over longer portions of the life cycle. PMID:25462312

  4. Knee Replacement Patients May Be Able to Hit the Shower Sooner

    MedlinePlus

    ... The study, led by Dr. Harold Rees, an orthopaedic surgeon at Loyola University Medical Center in Maywood, ... wrote. The findings were published online in the Journal of Arthroplasty . SOURCE: Loyola University Health System, news ...

  5. Distribution of rare earth elements and uranium in various components of ordinary chondrites

    NASA Astrophysics Data System (ADS)

    Ebihara, M.; Honda, M.

    1984-06-01

    Rare earth elements (REE) and uranium were studied for their distributions in various component phases of four ordinary chondrites. Kesen (H4), Richardton (H5), Bruderheim (L6), and Saint Severin (LL6). A selective dissolution method was applied for the phase fractionation. The REE were analysed by neutron activation analysis, and U was determined by neutron-induced fission tracks. The present study revealed that both REE and U are highly enriched in the Ca-phosphate minerals with different enrichment factors, implying chemical fractionation between them. The phosphates seem to be responsible for more than 80 percent of the light REE in all chondrites. On the other hand, only 20-40 percent of the total U resides in the Ca-phosphates. This difference in enrichments might have been caused through the levels of metamorphic activity on the meteoritic parent bodies.

  6. Theme: Serving Individuals with Disabilities.

    ERIC Educational Resources Information Center

    Frick, Marty; And Others

    1993-01-01

    Includes "Reviewing Commitment to Individuals with Disabilities" (Frick); "Modifying Laboratory Equipment" (Silletto); "Equine Facilitated Therapy" (Hoover et al.); "Horticultural Therapy" (Rees, Iverson); "How Accessible Is Your Agriculture Program? (Delks, Sillery); "Agricultural Education for the Mentally Handicapped" (Phillips, Dormody);…

  7. Rapeseed ethyl ester as bio-lube in 2-cycle engine

    SciTech Connect

    1996-12-31

    The performance of four blends of gasoline with rapeseed ethyl ester (REE) and three commercial 2-cycle oils has been evaluated in engine tests by the University of Idaho. Details and results of the tests are given in the article.

  8. Dr. Wernher Von Braun examines a ruby crystal.

    NASA Technical Reports Server (NTRS)

    1999-01-01

    Dr. Wernher Von Braun (right), director of the Marshall Space Flight Center, and Dr. Eberhard Rees (left), deputy director, technical, examine a ruby crystal used in laser experiments in the Marshall Center's Space Sciences Laboratory.