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Sample records for element isotopic compositions

  1. Isotopic compositions of the elements 2013 (IUPAC Technical Report)

    Science.gov (United States)

    Meija, Juris; Coplen, Tyler B.; Berglund, Michael; Brand, Willi A.; De Bièvre, Paul; Gröning, Manfred; Holden, Norman E.; Irrgeher, Johanna; Loss, Robert D.; Walczyk, Thomas; Prohaska, Thomas

    2016-01-01

    The Commission on Isotopic Abundances and Atomic Weights (ciaaw.org) of the International Union of Pure and Applied Chemistry (iupac.org) has revised the Table of Isotopic Compositions of the Elements (TICE). The update involved a critical evaluation of the recent published literature. The new TICE 2013 includes evaluated data from the “best measurement” of the isotopic abundances in a single sample, along with a set of representative isotopic abundances and uncertainties that accommodate known variations in normal terrestrial materials.

  2. Isotopic composition of chemical elements in natural cycles

    International Nuclear Information System (INIS)

    Wetzel, K.

    1977-12-01

    Mathematical models developed for planning and evaluating tracer experiments have been applied in investigations of the isotopic composition of carbon in its natural cycle through various periods of the last billion years. The influence on the natural isotope ratio due to industrial combustion of fossil fuels is shown. In order to describe regional differences from the global behaviour of carbon a parameter has been introduced, which represents the time needed for one total exchange of the atmosphere in a certain region with the global atmosphere

  3. Alkali elemental and potassium isotopic compositions of Semarkona chondrules

    Science.gov (United States)

    Alexander, C.M. O'D.; Grossman, J.N.

    2005-01-01

    We report measurements of K isotope ratios in 28 Semarkona chondrules with a wide range of petrologic types and bulk compositions as well as the compositions of CPX-mesostasis pairs in 17 type I Semarkona chondrules, including two chondrules with radial alkali zonation and 19 type II chondrules. Despite the wide range in K/Al ratios, no systematic variations in K isotopic compositions were found. Semarkona chondrules do not record a simple history of Rayleigh-type loss of K. Experimentally determined evaporation rates suggest that considerable alkali evaporation would have occurred during chondrule formation. Nevertheless, based on Na CPX-mesostasis distribution coefficients, the alkali contents of the cores of most chondrules in Semarkona were probably established at the time of final crystallization. However, Na CPX-mesostasis distribution coefficients also show that alkali zonation in type I Semarkona chondrules was produced by entry of alkalis after solidification, probably during parent body alteration. This alkali metasomatism may have gone to completion in some chondrules. Our preferred explanation for the lack of systematic isotopic enrichments, even in alkali depleted type I chondrule cores, is that they exchanged with the ambient gas as they cooled. ?? The Meteoritical Society, 2005.

  4. A Three End-Member Mixing Model Based on Isotopic Composition and Elemental Ratio

    Directory of Open Access Journals (Sweden)

    Kon-Kee Liu Shuh-Ji Kao

    2007-01-01

    Full Text Available A three end-member mixing model based on nitrogen isotopic composition and organic carbon to nitrogen ratio of suspended particulate matter in an aquatic environment has been developed. Mathematical expressions have been derived for the calculation of the fractions of nitrogen or organic carbon originating from three different sources of distinct isotopic and elemental compositions. The model was successfully applied to determine the contributions from anthropogenic wastes, soils and bedrock-derived sediments to particulate nitrogen and particulate organic carbon in the Danshuei River during the flood caused by Typhoon Bilis in August 2000. The model solutions have been expressed in a general form that allows applications to mixtures with other types of isotopic compositions and elemental ratios or in forms other than suspended particulate matter.

  5. Elemental and iron isotopic composition of aerosols collected in a parking structure

    International Nuclear Information System (INIS)

    Majestic, Brian J.; Anbar, Ariel D.; Herckes, Pierre

    2009-01-01

    The trace metal contents and iron isotope composition of size-resolved aerosols were determined in a parking structure in Tempe, AZ, USA. Particulate matter (PM) 2.5 μm were collected. Several air toxics (e.g., arsenic, cadmium, and antimony) were enriched above the crustal average, implicating automobiles as an important source. Extremely high levels of fine copper (up to 1000 ng m -3 ) were also observed in the parking garage, likely from brake wear. The iron isotope composition of the aerosols were found to be + 0.15 ± 0.03 per mille and + 0.18 ± 0.03 per mille for the PM 2.5 μm fractions, respectively. The similarity of isotope composition indicates a common source for each size fraction. To better understand the source of iron in the parking garage, the elemental composition in four brake pads (two semi-metallic and two ceramic), two tire tread samples, and two waste oil samples were determined. Striking differences in the metallic and ceramic brake pads were observed. The ceramic brake pads contained 10-20% copper by mass, while the metallic brake pads contained about 70% iron, with very little copper. Both waste oil samples contained significant amounts of calcium, phosphorous, and zinc, consistent with the composition of some engine oil additives. Differences in iron isotope composition were observed between the source materials; most notably between the tire tread (average = + 0.02 per mille ) and the ceramic brake linings (average = + 0.65 per mille ). Differences in isotopic composition were also observed between the metallic (average = + 0.18 per mille ) and ceramic brake pads, implying that iron isotope composition may be used to resolve these sources. The iron isotope composition of the metallic brake pads was found to be identical to the aerosols, implying that brake dust is the dominant source of iron in a parking garage.

  6. Using trace element content and lead isotopic composition to assess sources of PM in Tijuana, Mexico

    Science.gov (United States)

    Salcedo, D.; Castro, T.; Bernal, J. P.; Almanza-Veloz, V.; Zavala, M.; González-Castillo, E.; Saavedra, M. I.; Perez-Arvízu, O.; Díaz-Trujillo, G. C.; Molina, L. T.

    2016-05-01

    PM2.5 samples were collected at two urban sites (Parque Morelos (PQM) and CECyTE (CEC)) in Tijuana during the Cal-Mex campaign from May 24 to June 5, 2010. Concentration of trace elements (Mg, Al, Ti, V, Mn, Fe, Co, Ni, Zn, Cu, Ga, As, Se, Rb, Sr, Mo, Cd, Sn, Sb, Ba, La, Ce, and Pb), and Pb isotopic composition were determined in order to study the sources of PM impacting each site. Other chemical analysis (gravimetric, elemental and organic carbon (EC/OC), and polycyclic aromatic hydrocarbons (PAHs)), were also performed. Finally, back-trajectories were calculated to facilitate the interpretation of the chemical data. Trace elements results show that CEC is a receptor site affected by mixed regional sources: sea salt, mineral, urban, and industrial. On the other hand, PQM seems to be impacted mainly by local sources. In particular, Pb at CEC is of anthropogenic, as well as crustal origin. This conclusion is supported by the lead isotopic composition, whose values are consistent with a combination of lead extracted from US mines, and lead from bedrocks in the Mexican Sierras. Some of the time variability observed can be explained using the back-trajectories.

  7. Tetrathionate and Elemental Sulfur Shape the Isotope Composition of Sulfate in Acid Mine Drainage

    Directory of Open Access Journals (Sweden)

    Nurgul Balci

    2017-08-01

    Full Text Available Sulfur compounds in intermediate valence states, for example elemental sulfur, thiosulfate, and tetrathionate, are important players in the biogeochemical sulfur cycle. However, key understanding about the pathways of oxidation involving mixed-valance state sulfur species is still missing. Here we report the sulfur and oxygen isotope fractionation effects during the oxidation of tetrathionate (S4O62− and elemental sulfur (S° to sulfate in bacterial cultures in acidic conditions. Oxidation of tetrathionate by Acidithiobacillus thiooxidans produced thiosulfate, elemental sulfur and sulfate. Up to 34% of the tetrathionate consumed by the bacteria could not be accounted for in sulfate or other intermediate-valence state sulfur species over the experiments. The oxidation of tetrathionate yielded sulfate that was initially enriched in 34S (ε34SSO4−S4O6 by +7.9‰, followed by a decrease to +1.4‰ over the experiment duration, with an average ε34SSO4−S4O6 of +3.5 ± 0.2‰ after a month of incubation. We attribute this significant sulfur isotope fractionation to enzymatic disproportionation reactions occurring during tetrathionate decomposition, and to the incomplete transformation of tetrathionate into sulfate. The oxygen isotope composition of sulfate (δ18OSO4 from the tetrathionate oxidation experiments indicate that 62% of the oxygen in the formed sulfate was derived from water. The remaining 38% of the oxygen was either inherited from the supplied tetrathionate, or supplied from dissolved atmospheric oxygen (O2. During the oxidation of elemental sulfur, the product sulfate became depleted in 34S between −1.8 and 0‰ relative to the elemental sulfur with an average for ε34SSO4−S0 of −0.9 ± 0.2‰ and all the oxygen atoms in the sulfate derived from water with an average normal oxygen isotope fractionation (ε18OSO4−H2O of −4.4‰. The differences observed in δ18OSO4 and the sulfur isotope composition of sulfate (δ34SSO4

  8. Isotopic composition of the elements and their variation in nature: a preliminary report

    International Nuclear Information System (INIS)

    Holden, N.E.

    1977-03-01

    Data in the literature on isotopic abundance values and their variation in nature are reviewed. Recommended values are presented for the isotopic abundances of all stable elements, their natural variation, and the corresponding atomic weights of these elements. 2 tables, 133 references

  9. Sr and Nd isotopic and trace element compositions of Quaternary volcanic centers of the Southern Andes

    Science.gov (United States)

    Futa, K.; Stern, C.R.

    1988-01-01

    Isotopic compositions of samples from six Quaternary volcanoes located in the northern and southern extremities of the Southern Volcanic Zone (SVZ, 33-46??S) of the Andes and from four centers in the Austral Volcanic Zone (AVZ, 49-54??S) range for 87Sr 86Sr from 0.70280 to 0.70591 and for 143Nd 144Nd from 0.51314 to 0.51255. The ranges are significantly greater than previously reported from the southern Andes but are different from the isotopic compositions of volcanoes in the central and northern Andes. Basalts and basaltic andesites from three centers just north of the Chile Rise-Trench triple junction have 87Sr 86Sr, 143Nd 144Nd, La Yb, Ba La, and Hf Lu that lie within the relatively restricted ranges of the basic magmas erupted from the volcanic centers as far north as 35??S in the SVZ of the Andes. The trace element and Sr and Nd isotopic characteristics of these magmas may be explained by source region contamination of subarc asthenosphere, with contaminants derived from subducted pelagic sediments and seawater-altered basalts by dehydration of subducted oceanic lithosphere. In the northern extremity of the SVZ between 33?? and 34??S, basaltic andesites and andesites have higher 87Sr 86Sr, Rb Cs, and Hf Lu, and lower 143Nd 144Nd than basalts and basaltic andesites erupted farther south in the SVZ, which suggests involvement of components derived from the continental crust. In the AVZ, the most primitive sample, high-Mg andesite from the southernmost volcanic center in the Andes (54??S) has Sr and Nd isotopic compositions and K Rb and Ba La similar to MORB. The high La Yb of this sample suggests formation by small degrees of partial melting of subducted MORB with garnet as a residue. Samples from centers farther north in the AVZ show a regionally regular northward increase in SiO2, K2O, Rb, Ba, Ba La, and 87Sr 86Sr and decrease in MgO, Sr, K Rb, Rb Cs, and 143Nd 144Nd, suggesting increasingly greater degrees of fractional crystallization and associated intra

  10. The origin and evolution of chondrites recorded in the elemental and isotopic compositions of their macromolecular organic matter

    Science.gov (United States)

    Alexander, C. M. O.'D.; Fogel, M.; Yabuta, H.; Cody, G. D.

    2007-09-01

    Extraterrestrial organic matter in meteorites potentially retains a unique record of synthesis and chemical/thermal modification by parent body, nebular and even presolar processes. In a survey of the elemental and isotopic compositions of insoluble organic matter (IOM) from 75 carbonaceous, ordinary and enstatite chondrites, we find dramatic variations within and between chondrite classes. There is no evidence that these variations correlate with the time and/or location of chondrite formation, or with any primary petrologic or bulk compositional features that are associated with nebular processes (e.g., chondrule and volatile trace element abundances). Nor is there evidence for the formation of the IOM by Fischer-Tropsch-Type synthesis in the nebula or in the parent bodies. The elemental variations are consistent with thermal maturation and/or oxidation of a common precursor. For reasons that are unclear, there are large variations in isotopic composition within and between chondrite classes that do not correlate in a simple way with elemental composition or petrologic type. Nevertheless, because of the pattern of elemental variations with petrologic type and the lack of any correlation with the primary features of the chondrite classes, at present the most likely explanation is that all IOM compositional variations are the result of parent body processing of a common precursor. If correct, the range of isotopic compositions within and between chondrite classes implies that the IOM is composed of several isotopically distinct components whose relative stability varied with parent body conditions. The most primitive IOM is found in the CR chondrites and Bells (CM2). Isotopically, the IOM from these meteorites resembles the IOM in interplanetary dust particles. Chemically, their IOM resembles the CHON particles of comet Halley. Despite the large isotopic anomalies in the IOM from these meteorites, it is uncertain whether the IOM formed in the interstellar medium or

  11. The use of stable isotope compositions of selected elements in food origin control

    International Nuclear Information System (INIS)

    Wierzchnicki, R.

    2002-01-01

    Stable isotope ratios have been used widely for authentication of foodstuffs especially for detection of added water and sugar in fruit juices and wines. Hydrogen and oxygen composition are particularly interesting probes for geographical origin and authenticity identification. Carbon and nitrogen composition of fruits contains the finger-print of their metabolism and growing condition. Exemplary data are presented which demonstrated the usefulness of the Isotope Ratio Mass Spectrometry (IRMS) methods for authenticating wines and fruits (juice and pulp). (author)

  12. Changing compositions in the Iceland plume; Isotopic and elemental constraints from the Paleogene Faroe flood basalts

    DEFF Research Database (Denmark)

    Søager, Nina; Holm, Paul Martin

    2011-01-01

    Elemental and Sr, Nd, Hf and high precision Pb isotopic data are presented from 59 low-Ti and high-Ti lavas from the syn-break up part of the Faroe Flood Basalt Province. The depleted MORB-like low-Ti lavas erupted in the rift zone between the Faroe Islands and central East Greenland around......-type component similar in geochemistry to the Icelandic Öræfajökull lavas. This component is believed to be recycled pelagic sediments in the plume but it can alternatively be a local crustal or lithospheric mantle component. The enriched Faroe high-Ti lavas erupted inland from the rift have isotopic...... compositions very similar to the enriched Icelandic neo-volcanics and these lava suites apparently share the two enriched plume end-members IE1 and IE2 (Geochim. Cosmochim. Acta 68, 2, 2004). The lack of mixing between high and low-Ti melts at the time of break up, is explained by a zoned plume where only low...

  13. Amphiboles as indicators of mantle source contamination: Combined evaluation of stable H and O isotope compositions and trace element ratios

    NARCIS (Netherlands)

    Demény, A.; Harangi, S.; Vennemann, T.W.; Casillas, R.; Horváth, P.; Milton, A.J.; Mason, P.R.D.; Ulianov, A.

    2012-01-01

    Stable isotope and trace element compositions of igneous amphiboles from different tectonic settings (ocean island basalts, intraplate alkaline basalts, subduction-related andesitic complexes) were compiled to help understand the role of fluids and melts in subduction-related mantle metasomatism

  14. Paloma: In-situ Measurement of The Elemental and Isotopic Composition of The Mars Atmosphere

    Science.gov (United States)

    Chassefiere, E.; Jambon, A.; Berthelier, J.-J.; Correia, J.-J.; Covinhes, J.; Goulpeau, G.; Leblanc, F.; Malique, Ch.; Sarda, P.; Schaetzel, P.; Sabroux, J.-C.; Ferry, C.; Richon, P.; Pineau, J.-F.; Desjean, M.-C.

    The PALOMA instrument, presently under study in the frame of the NASA/CNES Mars exploration program, is devoted to the accurate measurement of isotopic and el- emental ratios in Mars atmosphere. It consists of a mass spectrometer coupled with a gas preparation line for separation of reactive and noble gas species, and noble gas species (and reactive gases) from each other, by chemical and cryogenic trapping, and possibly permeation techniques. This instrument, ranked among the most important four types of measurement recommended by the US Committee on Planetary and Lu- nar Exploration (COMPLEX), will be proposed as a part of the payload of the 07 NASA smart landers. The general objectives of PALOMA are to provide instanta- neous and time-varying patterns of noble gas isotopic spectra, and stable isotopes. Such measurements will allow to improve our general understanding of volatile cy- cles on Mars, and to better decipher the history of the atmosphere and climate. Past escape processes, exchanges between solid planet and atmosphere, post-accretional addition of volatil-rich matter from comets, are expected to have imprinted specific isotopic signatures. Although these signatures are strongly interlocked, a compara- tive Earth-Mars approach may allow to discriminate between them, and therefore to reconstruct the history of Martian volatiles. The evolution of atmospheric mass and composition may have had a major impact on climate evolution, e.g. through massive escape of carbon dioxide and water. In addition, precise measurements of isotopes in the present Mars atmosphere are the most promising way on the short term to confirm that SNC meteorites are from Martian origin. PALOMA also includes a small separate device for measuring ambient natural radioactivity, which might provide information about the presence of a near subsurface permafrost, possible residual volcanic activity, vertical mixing rate in the boundary layer.

  15. The application of scanning electron microscopy to the determination of elemental and isotopic composition in individual actinide particles

    International Nuclear Information System (INIS)

    Vatter, I.; Cattle, G.; Tushingham, J.

    2000-01-01

    Techniques for the determination of both elemental and isotopic composition of actinides within single particles are required by the IAEA in support of their environmental safeguards programme. SEM and SIMS are valuable techniques for the measurement of elemental and isotopic composition, respectively, on the particle scale. The potential for effective combination of SEM and SIMS has been investigated at Harwell Laboratory. In trials, copper finder grids have been successfully used to enable re-identification of particles between SEM and SIMS instruments. Use of the grids enables rapid relocation of particles pre-selected by SEM for SIMS measurement. The work has highlighted a possible matrix effect in plutonium measurement that results in variable sensitivity dependent on the presence of other elements (including uranium). This effect would limit the use of SIMS to obtain elemental ratios, and highlights the requirement to use both SEM and SIMS to gain full and accurate information. The possible use of autoradiography as an adjunct to SEM has been investigated. In principle, autoradiography could be used to identify higher enrichments of uranium and enable pre-selection of particles for SIMS measurement. During trials, practical problems have been encountered which have demonstrated this particular approach to be unsuitable. (author)

  16. Comparison of elemental, nutritional, and isotopic composition of Philippine and Japanese polished rice samples for provenance validation

    International Nuclear Information System (INIS)

    Pabroa, Preciosa Corazon B.; Sucgang, Raymond J.; Mendoza, Norman dS.; Ebihara, Mitsuru; Conanan, Aida P.; Nosotros, Ro-Ann S.

    2012-01-01

    Rice (Oryza sativa), has been considered the best staple food among all cereals and is the staple food for over 3 billion people, constituting over half of the world's population (Cantral and Reeves, 2002). In this study, elemental, isotopic and proximate analyses were done on rice samples in a attempt to establish variances between Philippine and Japanese rice, which can be useful for geographical authenticity testing. Rice samples were collected in Japan and in the Philippines (market survey samples from Metro Manila, and farm harvests from Aklan province). The samples were washed, dried and ground to fine powder. Instrumental neutron activation analysis (INAA), a very sensitive non-destructive multi-element analytical technique, was used for the elemental analysis of the samples and isotope-ratio mass spectrometry (IRMS) was used to obtain the isotopic signatures of the samples. Proximate analysis (AOAC procedure) was used to determine nutrient aggregates. Results show that compared with the unpolished rice standard NIES CRM10b, the polished Japanese and Philippine rice sampled show reduced concentrations of elements by as much as 1/10, 1/4, 1/5 and 1/3 for Mg, Mn, K and Na, respectively. Levels of Ca and Zn are not greatly affected. Arsenic is found in all the Japanese rice tested at an average concentration of 0.103 μg/g and three out of four of the Philippine rice at an average concentration of 0.070 μg/g. Arsenic contamination may have been introduced from the fertilizer used in rice fields. Higher levels of Br are seen in two of the Philippine rice at 14 and 34 μg/g with the most probable source being the pesticide methyl bromide. The rice samples from Aklan showed inter-variety variability in composition (70 to 85 % carbohydrates, 0.5 to 3.0 % fat and 4 to 5 % protein) which makes it difficult to establish provenance in terms of proximate composition. Isotopic ratio of δ 13 C show signature that of a C3 plant with possible narrow distinguishable

  17. Correlates of elemental-isotopic composition of stream fishes: the importance of land-use, species identity and body size.

    Science.gov (United States)

    Montaña, C G; Schalk, C M

    2018-04-01

    The isotopic (δ 13 C and δ 15 N) and stoichiometric (C:N:P) compositions of four fish species (Family Centrarchidae: Lepomis auritus, Lepomis cyanellus; Family Cyprinidae: Nocomis leptocephalus, Semotilus atromaculatus) were examined across four North Carolina Piedmont streams arrayed along an urbanization gradient. Both isotopic and stoichiometric composition of fishes appeared to track changes occurring in basal resource availability. Values of δ 13 C of basal resources and consumers were more enriched at the most urbanized streams. Similarly, basal resources and consumers were δ 15 N-enriched at more urbanized streams. Basal resource stoichiometry varied across streams, with periphyton being the most variable. Primary consumers stoichiometry also differed across streams. Intraspecific variation in fish stoichiometry correlated with the degree of urbanization, as the two cyprinids had higher N content and L. cyanellus had higher P content in more urbanized streams, probably due to enrichment of basal resources. Intrinsic factors, specifically species identity and body size also affected stoichiometric variation. Phosphorus (P) content increased significantly with body size in centrarchids, but not in cyprinids. These results suggest that although species identity and body size are important predictors of elemental stoichiometry, the complex nature of altered urban streams may yield imbalances in the elemental composition of consumers via their food resources. © 2018 The Fisheries Society of the British Isles.

  18. Ash layer at ∼ 8 Ma in ODP site 758 from the Bay of Bengal: evidence from Sr, Nd isotopic compositions and rare earth elements

    International Nuclear Information System (INIS)

    Padmakumari, V.M.; Ahmad, S.M.

    2004-01-01

    Strontium and neodymium isotopic compositions are widely used to delineate the provenance of sedimentary formations. These isotopes have characteristic signatures for crust and mantle material and therefore can distinguish between volcanic and other rock types. 87 Sr/ 86 Sr. ε Nd (0) and rare earth elements REE of clay sediments from ODP site 758 in the Bay of Bengal is reported here. Our results clearly show that Sr and Nd isotopes can identify thin ash layers that otherwise may not easily be recognized

  19. Macro elements and isotopic composition survey in a hydrographic basin in the Center Amazon

    International Nuclear Information System (INIS)

    Cunha Senna, Hillandia Brandao da.

    1992-07-01

    The study was conducted in a 3.5 Km 2 watershed located approximately 60 Km north from Manaus. It's main objective was to quantify major elements inputs through rainfall and outputs via river run-off, and to study the water routing by using water stable isotopes. The sampling was conducted in four different pluviometers and in the main channel of the watershed. The major elements Ca ++ , K + , P and Al do not showed significant temporal variability, however with a lower concentration in relation to other studies. The major elements budget showed a net gain of Mg + , Na ++ , Na ++ and N O 3 - , or the input fluxes were higher than the output fluxes. On the other hand, there was a net loss of K + , Al, Fe, and Cl - . The average values of the delta 18 O and delta Deuterium of the rain water was equal to -3,3% and -14,8% respectively. For the river water the average concentration was lighter than the rain, being equal to -5,1% and -26,1%. (author). 87 refs., 15 figs., 11 tabs

  20. Measurement of the isotopic composition of the primary cosmic radiation for the elements B-Ne

    International Nuclear Information System (INIS)

    Bjarle, C.; Herrstroem, N-Y.; Jacobsson, L.; Joensson, G.; Kristiansson, K.

    1977-05-01

    The results are given from an investigation of the isotopic composition of primary cosmic ray B, C, N and O. Preliminary result is also given from an investigation of Ne. The mass measurements are made in nuclear emulsions exposed at about 3 g/cm 2 atmospheric depth. The results for B-O represented as quotients extrapolated to the top of the atmosphere, are: 11 B/B=0.61+-0.10; 13 C/C=0.06+-0.03; 15 N/N=0.33+-0.09; 17 O/O=0.05+-0.03; 18 O/O=0.08+-0.03. The preliminary result from the Ne-measurements shows that nuclei with masses larger than 20 exist among the primary neon nuclei. (Auth.)

  1. Power of isotopic fine structure for unambiguous determination of metabolite elemental compositions: In silico evaluation and metabolomic application

    International Nuclear Information System (INIS)

    Nagao, Tatsuhiko; Yukihira, Daichi; Fujimura, Yoshinori; Saito, Kazunori; Takahashi, Katsutoshi; Miura, Daisuke; Wariishi, Hiroyuki

    2014-01-01

    Graphical abstract: - Highlights: • We developed a method to determine elemental composition of metabolites. • The method was based on mass spectral data and empirical constraints. • In the validation study, the method succeeded for 70% of detected peaks. - Abstract: In mass spectrometry (MS)-based metabolomics studies, reference-free identification of metabolites is still a challenging issue. Previously, we demonstrated that the elemental composition (EC) of metabolites could be unambiguously determined using isotopic fine structure, observed by ultrahigh resolution MS, which provided the relative isotopic abundance (RIA) of 13 C, 15 N, 18 O, and 34 S. Herein, we evaluated the efficacy of the RIA for determining ECs based on the MS peaks of 20,258 known metabolites. The metabolites were simulated with a ≤25% error in the isotopic peak area to investigate how the error size effect affected the rate of unambiguous determination of the ECs. The simulation indicated that, in combination with reported constraint rules, the RIA led to unambiguous determination of the ECs for more than 90% of the tested metabolites. It was noteworthy that, in positive ion mode, the process could distinguish alkali metal-adduct ions ([M + Na] + and [M + K] + ). However, a significant degradation of the EC determination performance was observed when the method was applied to real metabolomic data (mouse liver extracts analyzed by infusion ESI), because of the influence of noise and bias on the RIA. To achieve ideal performance, as indicated in the simulation, we developed an additional method to compensate for bias on the measured ion intensities. The method improved the performance of the calculation, permitting determination of ECs for 72% of the observed peaks. The proposed method is considered a useful starting point for high-throughput identification of metabolites in metabolomic research

  2. Primary magmas and mantle sources of Emeishan basalts constrained from major element, trace element and Pb isotope compositions of olivine-hosted melt inclusions

    Science.gov (United States)

    Ren, Zhong-Yuan; Wu, Ya-Dong; Zhang, Le; Nichols, Alexander R. L.; Hong, Lu-Bing; Zhang, Yin-Hui; Zhang, Yan; Liu, Jian-Qiang; Xu, Yi-Gang

    2017-07-01

    Olivine-hosted melt inclusions within lava retain important information regarding the lava's primary magma compositions and mantle sources. Thus, they can be used to infer the nature of the mantle sources of large igneous provinces, which is still not well known and of the subject of debate. We have analysed the chemical compositions and Pb isotopic ratios of olivine-hosted melt inclusions in the Dali picrites, Emeishan Large Igneous Province (LIP), SW China. These are the first in-situ Pb isotope data measured for melt inclusions found in the Emeishan picrites and allow new constraints to be placed on the source lithology of the Emeishan LIP. The melt inclusions show chemical compositional variations, spanning low-, intermediate- and high-Ti compositions, while their host whole rocks are restricted to the intermediate-Ti compositions. Together with the relatively constant Pb isotope ratios of the melt inclusions, the compositional variations suggest that the low-, intermediate- and high-Ti melts were derived from compositionally similar sources. The geochemical characteristics of melt inclusions, their host olivines, and whole-rocks from the Emeishan LIP indicate that Ca, Al, Mn, Yb, and Lu behave compatibly, and Ti, Rb, Sr, Zr, and Nb behave incompatibly during partial melting, requiring a pyroxenite source for the Emeishin LIP. The wide range of Ti contents in the melt inclusions and whole-rocks of the Emeishan basalts reflects different degrees of partial melting in the pyroxenite source at different depths in the melting column. The Pb isotope compositions of the melt inclusions and the OIB-like trace element compositions of the Emeishan basalts imply that mixing of a recycled ancient oceanic crust (EM1-like) component with a peridotite component from the lower mantle (FOZO-like component) could have underwent solid-state reaction, producing a secondary pyroxenite source that was subsequently partially melted to form the basalts. This new model of pyroxenite

  3. Review of footnotes and annotations to the 1949–2013 tables of standard atomic weights and tables of isotopic compositions of the elements (IUPAC Technical Report)

    Science.gov (United States)

    Coplen, Tyler B.; Holden, Norman E.

    2016-01-01

    The Commission on Isotopic Abundances and Atomic Weights uses annotations given in footnotes that are an integral part of the Tables of Standard Atomic Weights to alert users to the possibilities of quite extraordinary occurrences, as well as sources with abnormal atomic-weight values outside an otherwise acceptable range. The basic need for footnotes to the Standard Atomic Weights Table and equivalent annotations to the Table of Isotopic Compositions of the Elements arises from the necessity to provide users with information that is relevant to one or more elements, but that cannot be provided using numerical data in columns. Any desire to increase additional information conveyed by annotations to these Tables is tempered by the need to preserve a compact format and a style that can alert users, who would not be inclined to consult either the last full element-by-element review or the full text of a current Standard Atomic Weights of the Elements report. Since 1989, the footnotes of the Tables of Standard Atomic Weights and the annotations in column 5 of the Table of Isotopic Compositions of the Elements have been harmonized by use of three lowercase footnotes, “g”, “m”, and “r”, that signify geologically exceptionally specimens (“g”), modified isotopic compositions in material subjected to undisclosed or inadvertent isotopic fractionation (“m”), and the range in isotopic composition of normal terrestrial material prevents more precise atomic-weight value being given (“r”). As some elements are assigned intervals for their standard atomic-weight values (applies to 12 elements since 2009), footnotes “g” and “r” are no longer needed for these elements.

  4. Mercury in litterfall and sediment using elemental and isotopic composition of carbon and nitrogen in the mangrove of Southeastern Brazil

    Science.gov (United States)

    Fragoso, Cynara Pedrosa; Bernini, Elaine; Araújo, Beatriz Ferreira; Almeida, Marcelo Gomes de; Rezende, Carlos Eduardo de

    2018-03-01

    Mercury and elemental and isotopic compositions of carbon and nitrogen were determined in litterfall and sediments from the mangrove of the Paraíba do Sul River, Rio de Janeiro, Brazil. Total mercury (THg) and monomethylmercury (MMHg) concentrations in sediment ranged from 33 to 123 ng g-1 and 0.20-1.38 ng g-1, respectively. The δ13C in sediment varied from -29.4 to -26.5‰ and from 2.4 to 5.8‰ in δ15N. The THg concentration in litterfall and its annual input to the mangrove was 21 ± 2 ng g-1 and 16 ± 4 μg m-2 for the species Laguncularia racemosa, 18 ± 1 ng g-1 and 17 ± 3 μg m-2 for Rhizophora mangle, and 53 ± 4 ng g-1 and 33 ± 4 μg m-2 for Avicennia germinans, respectively. The isotopic composition of leaf litter ranged from -28.6 to -26.9‰ for δ13C and 4.5-7.2‰ for δ15N. Both the highest annual Hg input via litterfall and highest sediment Hg concentration were observed in areas dominated by A. germinans. These results suggest that the rate of litterfall of plant species and the atmospheric deposition have played an important role in the Hg biogeochemical cycle in the mangrove ecosystem.

  5. The stable isotope composition of nitrogen and carbon and elemental contents in modern and fossil seabird guano from Northern Chile - Marine sources and diagenetic effects.

    Directory of Open Access Journals (Sweden)

    Friedrich Lucassen

    Full Text Available Seabird excrements (guano have been preserved in the arid climate of Northern Chile since at least the Pliocene. The deposits of marine organic material in coastal areas potentially open a window into the present and past composition of the coastal ocean and its food web. We use the stable isotope composition of nitrogen and carbon as well as element contents to compare the principal prey of the birds, the Peruvian anchovy, with the composition of modern guano. We also investigate the impact of diagenetic changes on the isotopic composition and elemental contents of the pure ornithogenic sediments, starting with modern stratified deposits and extending to fossil guano. Where possible, 14C systematics is used for age information. The nitrogen and carbon isotopic composition of the marine prey (Peruvian anchovy of the birds is complex as it shows strong systematic variations with latitude. The detailed study of a modern profile that represents a few years of guano deposition up to present reveals systematic changes in nitrogen and carbon isotopic composition towards heavier values that increase with age, i.e. depth. Only the uppermost, youngest layers of modern guano show compositional affinity to the prey of the birds. In the profile, the simultaneous loss of nitrogen and carbon occurs by degassing, and non-volatile elements like phosphorous and calcium are passively enriched in the residual guano. Fossil guano deposits are very low in nitrogen and low in carbon contents, and show very heavy nitrogen isotopic compositions. One result of the study is that the use of guano for tracing nitrogen and carbon isotopic and elemental composition in the marine food web of the birds is restricted to fresh material. Despite systematic changes during diagenesis, there is little promise to retrieve reliable values of marine nitrogen and carbon signatures from older guano. However, the changes in isotopic composition from primary marine nitrogen isotopic

  6. Mantle heterogeneity in northeastern Africa: evidence from Nd isotopic compositions and hygromagmaphile element geochemistry of basaltic rocks from the Gulf of Tadjoura and southern Red Sea regions

    International Nuclear Information System (INIS)

    Barrat, J.A.; Jahn, B.M.; Auvray, B.; Hamdi, H.; Joron, J.L.

    1990-01-01

    Basaltic rocks from the Gulf of Tadjoura and southern Red Sea regions have been analysed for their Nd isotopic compositions and major and trace element concentrations. The wide variation in isotopic and geochemical compositions of the basaltic rocks is best explained by the mixing phenomenon involving a variety of mantle source components. To test the mixing hypothesis, a combined use of Nd isotopes and hygromagmaphile elemental ratios is proven very powerful. Three reservoirs have been identified as minimum components in their petrogenesis: (1) DMM (depleted MORB mantle), a mantle source depleted in light rare earth elements (LREE), which is the principal component of the N-MORB type basalts of this region; (2) REC (Ramad enriched component), equivalent to the hot-spot type of source detected in the south of Red Sea; (3) TEC (Tadjoura enriched component), a rather unique component located in the region of Tadjoura Gulf; it is characterised by a relative depletion in Rb, K, Th and U in a primitive mantle- or chondrite-normalised incompatible element pattern; this component could have been produced by mantle metasomatism of an originally depleted mantle. Mixing in various proportions of the above components is considered to be the principal mechanism for the formation of basalts with such diverse isotopic and trace element compositions. (orig.)

  7. Investigation of the isotopic composition of lead and of trace elements concentrations in natural uranium materials as a signature in nuclear forensics

    Energy Technology Data Exchange (ETDEWEB)

    Svedkauskaite-LeGore, J. [European Commission, Joint Research Centre, Karlsruhe (Germany). Inst. for Transuranium Elements; Institute of Physics, Vilnius (Lithuania); Mayer, K.; Millet, S.; Nicholl, A.; Rasmussen, G. [European Commission, Joint Research Centre, Karlsruhe (Germany). Inst. for Transuranium Elements; Baltrunas, D. [Institute of Physics, Vilnius (Lithuania)

    2007-07-01

    Lead is contained as trace element in uranium ores and propagates throughout the production process to intermediate products like yellow cake or uranium oxide. The lead isotopes in such material originate from two sources: natural lead and radiogenic lead. The variability of the isotopic composition of lead in ores and yellow cakes was studied and the applicability of this parameter for nuclear forensic investigations was investigated. Furthermore, the chemical impurities contained in these materials were measured in order to identify characteristic differences between materials from different mines. For the samples investigated, it could be shown, that the lead isotopic composition varies largely from mine to mine and it may be used as one of the parameters to distinguish between materials of different origins. Some of the chemical impurities show a similar pattern and support the conclusions drawn from the lead isotope data. (orig.)

  8. Trace element and isotopic compositions of Vietnamese basalts: implications for mantle dynamics in the southeast Asian region

    International Nuclear Information System (INIS)

    Nguyen, H.; Fower, M.; Nguyen, H.; Nguyen, X.B.; Nguyen, T.Y.

    1996-01-01

    Cenozoic basalts in Indo-China are part of a regional melting episode along the rifted Eurasian margin. Trace element and isotopic compositions of Vietnamese basalts are used to place constraints on the extent of lithospheric and asthenosphere contributions to the melts and possible mantle dynamic implications. The 87 Sr/ 86 Sr, 207 Pb/ 204 Pb, and 208 Pb/ 204 Pb isotopic ratios of the basalts reflect minimal crustal wall rock reaction, and variable enrichment in EM1 and EM2 of a 208 Pb-rich MORB-like source. Some, but not all, of this variation corresponds to the age of lithospheric sector penetrated. Basalts erupted through a cratonic, central sector (e.g. at Quang Ngai, Pleiku, Song Cau, Kong Plong, and Buon Ma Thuot) and off-cratonic, southwest sector (e.g. Phuoc Long) resemble those of EM2-rich basalts from southern and southeaster China and the South China Sea. Basalts from an off-cratonic, southeast sector (e.g. from Dalat, Xuan Loc, and the offshore Ile des Cendres-Phu Cuy complex) reflect mixing between a low- 206 Pb/ 204 Pb, high- 208 Pb/ 204 Pb, EM1-like component, and resemble basalts from northwest Taiwan, eastern and northeastern China, and parts of the Japan Sea. While EM2 tends to characterise lithospheric sectors, presence of EM1 in off-cratonic rather than cratonic basalts implies an asthenosphere rather than lithospheric source. Pervasive presence of EM1 in southeast Asian and marginal basin asthenosphere corresponds with thermally-anomalous mantle and may involve delaminated cratonic substrate entrained by mobile, extruded asthenosphere. (authors)

  9. Source of boron in the Palokas gold deposit, northern Finland: evidence from boron isotopes and major element composition of tourmaline

    Science.gov (United States)

    Ranta, Jukka-Pekka; Hanski, Eero; Cook, Nick; Lahaye, Yann

    2017-06-01

    The recently discovered Palokas gold deposit is part of the larger Rompas-Rajapalot gold-mineralized system located in the Paleoproterozoic Peräpohja Belt, northern Finland. Tourmaline is an important gangue mineral in the Palokas gold mineralization. It occurs as tourmalinite veins and as tourmaline crystals in sulfide-rich metasomatized gold-bearing rocks. In order to understand the origin of tourmaline in the gold-mineralized rocks, we have investigated the major element chemistry and boron isotope composition of tourmaline from three areas: (1) the Palokas gold mineralization, (2) a pegmatitic tourmaline granite, and (3) the evaporitic Petäjäskoski Formation. Based on textural evidence, tourmaline in gold mineralization is divided into two different types. Type 1 is located within the host rock and is cut by rock-forming anthophyllite crystals. Type 2 occurs in late veins and/or breccia zones consisting of approximately 80% tourmaline and 20% sulfides, commonly adjacent to quartz veins. All the studied tourmaline samples belong to the alkali-group tourmaline and can be classified as dravite and schorl. The δ11B values of the three localities lie in the same range, from 0 to -4‰. Tourmaline from the Au mineralization and from the Petäjäskoski Formation has similar compositional trends. Mg is the major substituent for Al; inferred low Fe3+/Fe2+ ratios and Na values (molybdenite related to the tourmaline-sulfide-quartz veins, we propose that the tourmaline-forming process is a result of a single magmatic-hydrothermal event related to the extensive granite magmatism at around 1.79-1.77 Ga. Tourmaline was crystallized throughout the hydrothermal process, which resulted in the paragenetic variation between type 1 and type 2. The close association of tourmaline and gold suggests that the gold precipitated from the same boron-rich source as tourmaline.

  10. DETERMINING THE ELEMENTAL AND ISOTOPIC COMPOSITION OF THE PRESOLAR NEBULA FROM GENESIS DATA ANALYSIS: THE CASE OF OXYGEN.

    Science.gov (United States)

    Laming, J Martin; Heber, V S; Burnett, D S; Guan, Y; Hervig, R; Huss, G R; Jurewicz, A J G; Koeman-Shields, E C; McKeegan, K D; Nittler, L; Reisenfeld, D B; Rieck, K D; Wang, J; Wiens, R C; Woolum, D S

    2017-12-10

    We compare element and isotopic fractionations measured in solar wind samples collected by NASA's Genesis mission with those predicted from models incorporating both the ponderomotive force in the chromosphere and conservation of the first adiabatic invariant in the low corona. Generally good agreement is found, suggesting that these factors are consistent with the process of solar wind fractionation. Based on bulk wind measurements, we also consider in more detail the isotopic and elemental abundances of O. We find mild support for an O abundance in the range 8.75 - 8.83, with a value as low as 8.69 disfavored. A stronger conclusion must await solar wind regime specific measurements from the Genesis samples.

  11. Paloma: an instrument to measure the molecular, elemental and isotopic composition of the mars atmosphere from a landed platform (MSL 09, EXOMARS)

    Energy Technology Data Exchange (ETDEWEB)

    Sabroux, J.Ch

    2003-07-01

    An instrument to analyze the molecular, elemental and isotopic composition of Mars atmosphere from a landed platform is being developed under CNES funding. This instrument, called PALOMA (Payload for Local Observation of Mars Atmosphere), will be proposed in response to the AO for the instrumentation of the NASA Mars Smart Lander mission, planned to be launched in 2009. It might be part as well of the EXOMARS mission presently studied at ESA in the frame of the Aurora program. Noble gases (He, Ne, Ar, Xr, Xe) and stable isotopes (C, H, O, N) will be analyzed by using a system of gas purification and separation, coupled with a mass spectrometer. The heaviest, radioactive, noble gas (Rn) and its short-lived daughters will be measured using a small additional device (alpha particle detector). Detailed search for trace constituents of astro-biological interest, like CH{sub 4}, H{sub 2}CO, N{sub 2}O, H{sub 2}S (abundances, isotopic ratios, time variability) will be done on a regular temporal basis during one Martian year. Isotopic ratios will be measured with an accuracy of about 1 ppm, or better, in order to provide a clear diagnosis of possible life signatures, to allow a detailed comparison of Earth and Mars atmospheric fractionation patterns and, finally, to accurately disentangle escape, climatic, geochemical and hypothesized biological effects. High sensitivity is required for elemental and isotopic compositions of trace gases of interest. Such an accurate monitoring of Mars atmosphere volatile composition is expected to provide the necessary reference for future composition studies of minerals, soils, bio-markers, polar cap material, either by in-situ measurement, or from laboratory analyses of returned samples. (author)

  12. Paloma: an instrument to measure the molecular, elemental and isotopic composition of the mars atmosphere from a landed platform (MSL 09, EXOMARS)

    International Nuclear Information System (INIS)

    Sabroux, J.Ch.

    2003-01-01

    An instrument to analyze the molecular, elemental and isotopic composition of Mars atmosphere from a landed platform is being developed under CNES funding. This instrument, called PALOMA (Payload for Local Observation of Mars Atmosphere), will be proposed in response to the AO for the instrumentation of the NASA Mars Smart Lander mission, planned to be launched in 2009. It might be part as well of the EXOMARS mission presently studied at ESA in the frame of the Aurora program. Noble gases (He, Ne, Ar, Xr, Xe) and stable isotopes (C, H, O, N) will be analyzed by using a system of gas purification and separation, coupled with a mass spectrometer. The heaviest, radioactive, noble gas (Rn) and its short-lived daughters will be measured using a small additional device (alpha particle detector). Detailed search for trace constituents of astro-biological interest, like CH 4 , H 2 CO, N 2 O, H 2 S (abundances, isotopic ratios, time variability) will be done on a regular temporal basis during one Martian year. Isotopic ratios will be measured with an accuracy of about 1 ppm, or better, in order to provide a clear diagnosis of possible life signatures, to allow a detailed comparison of Earth and Mars atmospheric fractionation patterns and, finally, to accurately disentangle escape, climatic, geochemical and hypothesized biological effects. High sensitivity is required for elemental and isotopic compositions of trace gases of interest. Such an accurate monitoring of Mars atmosphere volatile composition is expected to provide the necessary reference for future composition studies of minerals, soils, bio-markers, polar cap material, either by in-situ measurement, or from laboratory analyses of returned samples. (author)

  13. U-Pb isotope and trace element compositions of pyrites in the Black Reef: implications on their age and origin

    International Nuclear Information System (INIS)

    Barton, E.S.

    1990-01-01

    In the Black Reef Quartzite Formation of the Transvaal Supergroup two gold-bearing conglomerate facies have been recognized. The source of gold in these reefs has long been a matter of speculation. Although some ascribe the gold and pyrite to a hydrothermal origin, the prevailing opinion favours a detrital origin. As a possible source, the reworked underlying sub-outcrops of the Kimberly Reef horizons in the Central Rand group have been proposed. An investigation was undertaken with the aim of defining the Pb-isotopic and trace element signatures of morphologically different pyrite populations within the two Black Reef facies as well as for the underlying Kimberly Reef. 2 tabs

  14. The role of soil biogeochemistry in wine taste: Soil factors influencing grape elemental composition, photosynthetic biomarkers and Cu/Zn isotopic signature of Vitis vinifera

    Science.gov (United States)

    Blotevogel, Simon; Oliva, Priscia; Darrozes, José; Viers, Jérôme; Audry, Stéphane; Courjault-Radé, Pierre; Orgogozo, Laurent; Le Guedard, Marina; Schreck, Eva

    2015-04-01

    Understanding the influence of soil composition in wine taste is of great economic and environmental interest in France and around the world. Nevertheless the impact of soil composition on wine taste is still controversially discussed. Since inorganic soil components do not have a proper taste and do not enter the plant anyway, their influence needs to be induced by nutrient absorption and its impact on plant functioning and grape composition. Indeed recent development of geological tracers of origin proof the existence of soil chemical and isotopic signatures in wine. However, type and scale of the impact of soil composition on wine taste are not well understood yet, and little experimental evidence exists due to the complexity of mechanisms involved. Thus, to provide evidence for the impact of soil composition on grape composition and potentially wine taste, we studied soil and plant material from two relevant vineyards (Soave, Italia). On those two directly adjacent vineyards, two different wines are produced with the same plant material and cultivation techniques. The vineyards only differ by their underlying bedrock - limestone versus basaltic rock - and thus present suitable conditions for investigating the impact of soil composition on grapes and wine. Pedological and mineralogical parameters were analyzed for the two vineyards whereas chemical extractions (citrate, CaCl2) were performed to determine nutrient bioavailability in both soils. Elemental compositions were determined by ICP-MS analyses in different compartments (soils, vine leaves and grapes). Isotopic fractionation of Cu and Zn was investigated in various samples as source tracers and in order to better understand fractionation mechanisms involved. Finally, plant health was studied using the Omega-3 biomarker which determines the fatty acid composition in vine leaves, directly involved in photosynthetic processes. Results show that the vineyards are characterized by two different soil types due

  15. PALOMA : An instrument to measure the molecular, elemental and isotopic composition of Mars atmosphere from a landed platform (MSL 09, EXOMARS)

    Science.gov (United States)

    Chassefière, E.; Paloma Team

    2003-04-01

    An instrument to analyze the molecular, elemental and isotopic composition of Mars atmosphere from a landed platform is being developed under CNES funding. This instrument, called PALOMA (PAyload for Local Observation of Mars Atmosphere), will be proposed in response to the AO for the instrumentation of the NASA Mars Smart Lander mission, planned to be launched in 2009. It might be part as well of the EXOMARS mission presently studied at ESA in the frame of the Aurora program. Noble gases (He, Ne, Ar, Xr, Xe) and stable isotopes (C, H, O, N) will be analyzed by using a system of gas purification and separation, coupled with a mass spectrometer. The heaviest, radioactive, noble gas (Rn) and its short-lived daughters will be measured using a small additional device (alpha particle detector). Detailed search for trace constituents of astrobiological interest, like CH_4, H_2CO, N_2O, H_2S (abundances, isotopic ratios, time variability) will be done on a regular temporal basis during one Martian year. Isotopic ratios will be measured with an accuracy of about 1 ppm, or better, in order to provide a clear diagnosis of possible life signatures, to allow a detailed comparison of Earth and Mars atmospheric fractionation patterns and, finally, to accurately disentangle escape, climatic, geochemical and hypothesized biological effects. High sensitivity is required for elemental and isotopic compositions of trace gases of interest (a small fraction of ppbv). Such an accurate monitoring of Mars atmosphere volatile composition is expected to provide the necessary reference for future composition studies of minerals, soils, bio-markers, polar cap material, either by in-situ measurement, or from laboratory analyses of returned samples. The PALOMA instrument consists of : a gas purification and separation line, using techniques of chemical and cryogenic trapping, and possibly membrane permeation, a mass spectrometer working in static mode, a turbo-molecular pump that provides the

  16. petrography, compositional characteristics and stable isotope ...

    African Journals Online (AJOL)

    PROF EKWUEME

    Subsurface samples of the predominantly carbonate Ewekoro Formation, obtained from Ibese core hole within the Dahomey basin were used in this study. Investigations entail petrographic, elemental composition as well as stable isotopes (carbon and oxygen) geochemistry in order to deduce the different microfacies and ...

  17. Determination of elemental impurities and U and O isotopic compositions with a view to identify the geographical and industrial origins of uranium ore concentrates

    Science.gov (United States)

    Salaun, A.; Hubert, A.; Pointurier, F.; Aupiais, J.; Pili, E.; Richon, P.; Fauré, A.; Diallo, S.

    2012-12-01

    First events of illicit trafficking of nuclear and radiological materials occurred 50 years ago. Nuclear forensics expertise are aiming at determining the use of seized material, its industrial history and provenance (geographical area, place of production or processing), at assisting in the identification and dismantling of illicit trafficking networks. This information is also valuable in the context of inspections of declared facilities to verify the consistency of operator's declaration. Several characteristics can be used to determine the origin of uranium ore concentrates such as trace elemental impurity patterns (Keegan et al., 2008 ; Varga et al., 2010a, 2010b) or uranium, oxygen and lead isotopic compositions (Tamborini et al., 2002a, 2002b ; Wallenius et al., 2006; Varga et al., 2009). We developed analytical procedures for measuring the isotopic compositions of uranium (234U/238U and 235U/238U) and oxygen (18O/16O) and levels of elemental impurities (e.g. REE, Th) from very small amounts of uranium ore concentrates (or yellow cakes). Micrometer particles and few milligrams of material are used for oxygen isotope measurements and REE determination, respectively. Reference materials were analyzed by mass spectrometry (TIMS, SF-ICP-MS and SIMS) to validate testing protocols. Finally, materials of unknown origin were analyzed to highlight significant differences and determine whether these differences allow identifying the origin of these ore concentrates. References: Keegan, E., et al. (2008). Applied Geochemistry 23, 765-777. Tamborini, G., et al. (2002a). Analytical Chemistry 74, 6098-6101. Tamborini, G., et al. (2002b). Microchimica Acta 139, 185-188. Varga, Z., et al. (2009). Analytical Chemistry 81, 8327-8334. Varga, Z., et al. (2010a). Talanta 80, 1744-1749. Varga, Z., et al. (2010b). Radiochimica Acta 98, 771-778 Wallenius, M., et al. (2006). Forensic Science International 156, 55-62.

  18. Heterogeneity of elemental composition and natural abundance of stables isotopes of C and N in soils and leaves of mangroves at their southernmost West Atlantic range.

    Science.gov (United States)

    Tognella, M M P; Soares, M L G; Cuevas, E; Medina, E

    2016-01-01

    Mangrove communities were selected in the state of Santa Catarina, Brazil, near their southernmost limit of distribution, to study mineral nutrient relation in soils and plants. Communities included three true mangrove species, Rhizophora mangle, Laguncularia racemosa and Avicennia germinans, and two associated species, the fern Acrostichum danaeifolium, and the grass Spartina densiflora. The sites included communities in the lower Río Tavares near Florianopolis city, Sonho beach near Palhoça city, and the Santo Antonio lagoon. These sites included a full range of mangroves under humid climate where winter temperatures, instead of salinity, may be the main factor regulating their productive capacity and species composition. Soil salinity was determined by the concentration of soluble Na, and soil C and N were linearly correlated indicating their association in organic matter. Tavares site showed higher specific conductivity, and concentrations of Na and Mg in the soil layer below 40 cm depth, indicating larger influence of marine water. Isotopic signature of C increased with soil depth suggesting that microorganisms decomposing organic matter are releasing 13C depleted CO2. Nitrogen isotopic signature decreased with soil depth, indicating enrichment in 15N possibly as a result of denitrification in the upper soil layers. Mineral elements in leaf tissues showed A. schaueriana with higher concentrations of N, P, Na, K, Cu, Zn, and Na/Ca ratio. Spartina densiflora was characterized by the lowest N and K concentrations, and the highest concentrations of Al and Fe. Rhizophora mangle and L. racemosa had the highest Ca concentrations. Carbon isotopic signatures identified S. densiflora as a C4 plant, and A. schaueriana as the mangrove species occupying comparatively more water stressed microsites than the rest. Leaf nitrogen isotopic signatures were positive, in correspondence with the soil values. The results support the hypothesis that sites sampled were comparatively

  19. Trace element and isotopic compositions of Vietnamese basalts: implications for mantle dynamics in the southeast Asian region; Compositions isotopiques et en elements en trace des basaltes vietnamiens: implications pour la dynamique du manteau en Asie du Sud-Est

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen, H.; Fower, M. [Illinois Univ., Chicago, IL (United States); Nguyen, H. [Tokyo Univ. (Japan); Nguyen, X.B.; Nguyen, T.Y. [Institute of Nuclear Science and Technology, Hanoi (Viet Nam)

    1996-12-31

    Cenozoic basalts in Indo-China are part of a regional melting episode along the rifted Eurasian margin. Trace element and isotopic compositions of Vietnamese basalts are used to place constraints on the extent of lithospheric and asthenosphere contributions to the melts and possible mantle dynamic implications. The {sup 87}Sr/{sup 86}Sr, {sup 207}Pb/{sup 204}Pb, and {sup 208}Pb/{sup 204}Pb isotopic ratios of the basalts reflect minimal crustal wall rock reaction, and variable enrichment in EM1 and EM2 of a {sup 208}Pb-rich MORB-like source. Some, but not all, of this variation corresponds to the age of lithospheric sector penetrated. Basalts erupted through a cratonic, central sector (e.g. at Quang Ngai, Pleiku, Song Cau, Kong Plong, and Buon Ma Thuot) and off-cratonic, southwest sector (e.g. Phuoc Long) resemble those of EM2-rich basalts from southern and southeaster China and the South China Sea. Basalts from an off-cratonic, southeast sector (e.g. from Dalat, Xuan Loc, and the offshore Ile des Cendres-Phu Cuy complex) reflect mixing between a low- {sup 206}Pb/{sup 204}Pb, high-{sup 208}Pb/{sup 204}Pb, EM1-like component, and resemble basalts from northwest Taiwan, eastern and northeastern China, and parts of the Japan Sea. While EM2 tends to characterise lithospheric sectors, presence of EM1 in off-cratonic rather than cratonic basalts implies an asthenosphere rather than lithospheric source. Pervasive presence of EM1 in southeast Asian and marginal basin asthenosphere corresponds with thermally-anomalous mantle and may involve delaminated cratonic substrate entrained by mobile, extruded asthenosphere. (authors) 85 refs.

  20. Heterogeneity of elemental composition and natural abundance of stables isotopes of C and N in soils and leaves of mangroves at their southernmost West Atlantic range

    Directory of Open Access Journals (Sweden)

    M. M. P. Tognella

    Full Text Available Abstract Mangrove communities were selected in the state of Santa Catarina, Brazil, near their southernmost limit of distribution, to study mineral nutrient relation in soils and plants. Communities included three true mangrove species, Rhizophora mangle, Laguncularia racemosa and Avicennia germinans, and two associated species, the fern Acrostichum danaeifolium, and the grass Spartina densiflora. The sites included communities in the lower Río Tavares near Florianopolis city, Sonho beach near Palhoça city, and the Santo Antonio lagoon. These sites included a full range of mangroves under humid climate where winter temperatures, instead of salinity, may be the main factor regulating their productive capacity and species composition. Soil salinity was determined by the concentration of soluble Na, and soil C and N were linearly correlated indicating their association in organic matter. Tavares site showed higher specific conductivity, and concentrations of Na and Mg in the soil layer below 40 cm depth, indicating larger influence of marine water. Isotopic signature of C increased with soil depth suggesting that microorganisms decomposing organic matter are releasing 13C depleted CO2. Nitrogen isotopic signature decreased with soil depth, indicating enrichment in 15N possibly as a result of denitrification in the upper soil layers. Mineral elements in leaf tissues showed A. schaueriana with higher concentrations of N, P, Na, K, Cu, Zn, and Na/Ca ratio. Spartina densiflora was characterized by the lowest N and K concentrations, and the highest concentrations of Al and Fe. Rhizophora mangle and L. racemosa had the highest Ca concentrations. Carbon isotopic signatures identified S. densiflora as a C4 plant, and A. schaueriana as the mangrove species occupying comparatively more water stressed microsites than the rest. Leaf nitrogen isotopic signatures were positive, in correspondence with the soil values. The results support the hypothesis that

  1. Trace-element and Sr, Nd, Pb, and O isotopic composition of Pliocene and Quaternary alkali basalts of the Patagonian Plateau lavas of southernmost South America

    Science.gov (United States)

    Stern, C.R.; Frey, F.A.; Futa, K.; Zartman, R.E.; Peng, Z.; Kurtis, Kyser T.

    1990-01-01

    The Pliocene and Quaternary Patagonian alkali basalts of southernmost South America can be divided into two groups. The "cratonic" basalts erupted in areas of Cenozoic plateau volcanism and continental sedimentation and show considerable variation in 87Sr/86Sr (0.70316 to 0.70512), 143Nd/144Nd (e{open}Nd) and 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios (18.26 to 19.38, 15.53 to 15.68, and 38.30 to 39.23, respectively). These isotopic values are within the range of oceanic island basalts, as are the Ba/La, Ba/Nb, La/Nb, K/Rb, and Cs/Rb ratios of the "cratonic" basalts. In contrast, the "transitional" basalts, erupted along the western edge of the outcrop belt of the Pliocene and Quaternary plateau lavas in areas that were the locus of earlier Cenozoic Andean orogenic arc colcanism, have a much more restricted range of isotopic composition which can be approximated by 87Sr/86Sr=0.7039??0.0004, e{open}Nd, 206Pb/204Pb=18.60??0.08, 207Pb/204Pb=15.60??0.01, and 208Pb/204Pb=38.50??0.10. These isotopic values are similar to those of Andean orogenic are basalts and, compared to the "cratonic" basalts, are displaced to higher 87Sr/86Sr at a given 143Nd/144Nd and to higher 207Pb/204Pb at a given 208Pb/204Pb. The "transitional" basalts also have Ba/La, Ba/Nb, La/Nb, and Cs/Rb ratios higher than the "cratonic" and oceanic island basalts, although not as high as Andean orogenic are basalts. In contrast to the radiogenic isotopes, ??18O values for both groups of the Patagonian alkali basalts are indistinguishable and are more restricted than the range reported for Andean orogenic are basalts. Whole rock ??18O values calculated from mineral separates for both groups range from 5.3 to 6.5, while measured whole rock ??18O values range from 5.1 to 7.8. The trace element and isotopic data suggest that decreasing degrees of partial melting in association with lessened significance of subducted slabderived components are fundamental factors in the west to east transition from arc

  2. Major, Trace Element Concentration and Triple-Oxygen Isotope Compositions of G- and I-Type Spherules from the Sør Rondane Mountains, East Antarctica

    Science.gov (United States)

    Soens, B.; Goderis, S.; Greenwood, R. C.; McKibbin, S.; Van Ginneken, M.; Vanhaecke, F.; Debaille, V.; Franchi, I. A.; Claeys, Ph.

    2017-07-01

    We present new major, trace element concentration (LA-ICP-MS) and triple-oxygen isotope (LF-IRMS) data for G- and I-type cosmic spherules. This study suggests that both types of micrometeorites may originate from ordinary chondrite parent bodies.

  3. Water mass circulation and weathering inputs in the Labrador Sea based on coupled Hf-Nd isotope compositions and rare earth element distributions

    Science.gov (United States)

    Filippova, Alexandra; Frank, Martin; Kienast, Markus; Rickli, Jörg; Hathorne, Ed; Yashayaev, Igor M.; Pahnke, Katharina

    2017-02-01

    The Labrador Sea is one of the key areas for deep water formation driving the Atlantic thermohaline circulation and thus plays an important role in Northern Hemisphere climatic fluctuations. In order to better constrain the overturning processes and the origins of the distinct water masses, combined dissolved Hf-Nd isotopic compositions and rare earth element (REE) distribution patterns were obtained from four water depth profiles along a section across the Labrador Sea. These were complemented by one surface sample off the southern tip of Greenland, three shallow water samples off the coast of Newfoundland, and two deep water samples off Nova Scotia. Although light REEs are markedly enriched in the surface waters off the coast of Newfoundland compared to north Atlantic waters, the REE concentration profiles are essentially invariant throughout the water column across the Labrador Sea. The hafnium concentrations of surface waters exhibit a narrow range between 0.6 and 1 pmol/kg but are not significantly higher than at depth. Neodymium isotope signatures (ɛNd) vary from unradiogenic values between -16.8 and -14.9 at the surface to more radiogenic values near -11.0 at the bottom of the Labrador Sea mainly reflecting the advection of the Denmark Strait Overflow Water and North East Atlantic Deep Water, the signatures of which are influenced by weathering contributions from Icelandic basalts. Unlike Nd, water column radiogenic Hf isotope signatures (ɛHf) are more variable representing diverse weathering inputs from the surrounding landmasses. The least radiogenic seawater ɛHf signatures (up to -11.7) are found in surface waters close to Greenland and near the Canadian margin. This reflects the influence of recirculating Irminger Current Waters, which are affected by highly unradiogenic inputs from Greenland. A three to four ɛHf unit difference is observed between Denmark Strait Overflow Water (ɛHf ∼ -4) and North East Atlantic Deep Water (ɛHf ∼ -0

  4. Platinum-group elements and gold in base metal sulfides, platinum-group minerals, and Re-Os isotope compositions of the Uitkomst complex, South Africa

    Czech Academy of Sciences Publication Activity Database

    Trubač, Jakub; Ackerman, Lukáš; Gauert, Ch.; Ďurišová, Jana; Hrstka, Tomáš

    2018-01-01

    Roč. 113, č. 2 (2018), s. 439-461 ISSN 0361-0128 R&D Projects: GA ČR GA13-15390S Institutional support: RVO:67985831 Keywords : binary alloys * copper compounds * economic geology * gold * iridium * isotopes * ore deposits * osmium * palladium * platinum * platinum metals * pyrites * Rhenium * rhenium alloys * ruthenium * solid solutions * sulfur compounds * crustal materials * mass-balance calculations * massive sulfides * mineralized zone * monosulfide solid solutions * platinum group elements * platinum group elements (PGEs) * platinum group minerals Subject RIV: DB - Geology ; Mineralogy; AC - Archeology, Anthropology, Ethnology (ARUB-Q) OBOR OECD: Geology; Archaeology (ARUB-Q) Impact factor: 2.519, year: 2016

  5. Assignment of element and isotope factors

    International Nuclear Information System (INIS)

    Schneider, R.A.

    1984-01-01

    Element and isotope factors are assigned in the NICS internal accounting system at the Exxon Fuel Fabrication Facility on the basis of coded information included on the material transfer documents. This paper explains more fully the manner in which NICS assigns these factors

  6. Isotopic composition of cosmic ray nuclei

    International Nuclear Information System (INIS)

    Enge, W.

    1976-01-01

    A review will be given on the role of cosmic ray isotopes as tracers of the astrophysical nucleo-synthesis. The products of every nuclear burning chain are first of all isotopes and not elements. Thus, it is the study of the isotopes rather than that of the elements that responds to the questions on these nucleo-synthetic reactions. The problems concerning the solar system isotopic abundances and the cosmic ray isotopic abundances as well as a comparison between both will be presented. Furthermore the present stage of the experimental techniques and the latest results will be discussed. (orig.) [de

  7. OXYGEN ISOTOPIC COMPOSITIONS OF SOLAR CORUNDUM GRAINS

    International Nuclear Information System (INIS)

    Makide, Kentaro; Nagashima, Kazuhide; Huss, Gary R.; Krot, Alexander N.

    2009-01-01

    Oxygen is one of the major rock-forming elements in the solar system and the third most abundant element of the Sun. Oxygen isotopic composition of the Sun, however, is not known due to a poor resolution of astronomical spectroscopic measurements. Several Δ 17 O values have been proposed for the composition of the Sun based on (1) the oxygen isotopic measurements of the solar wind implanted into metallic particles in lunar soil ( 2 O 3 ) is thermodynamically the first condensate from a cooling gas of solar composition. Corundum-bearing CAIs, however, are exceptionally rare, suggesting either continuous reaction of the corundum condensates with a cooling nebular gas and their replacement by hibonite (CaAl 12 O 19 ) or their destruction by melting together with less refractory condensates during formation of igneous CAIs. In contrast to the corundum-bearing CAIs, isolated micrometer-sized corundum grains are common in the acid-resistant residues from unmetamorphosed chondrites. These grains could have avoided multistage reprocessing during CAI formation and, therefore, can potentially provide constraints on the initial oxygen isotopic composition of the solar nebula, and, hence, of the Sun. Here we report oxygen isotopic compositions of ∼60 micrometer-sized corundum grains in the acid-resistant residues from unequilibrated ordinary chondrites (Semarkona (LL3.0), Bishunpur (LL3.1), Roosevelt County 075 (H3.2)) and unmetamorphosed carbonaceous chondrites (Orgueil (CI1), Murray (CM2), and Alan Hills A77307 (CO3.0)) measured with a Cameca ims-1280 ion microprobe. All corundum grains, except two, are 16 O-rich (Δ 17 O = -22.7 per mille ± 8.5 per mille, 2σ), and compositionally similar to the mineralogically pristine CAIs from the CR carbonaceous chondrites (-23.3 per mille ± 1.9 per mille, 2σ), and solar wind returned by the Genesis spacecraft (-27 per mille ± 6 per mille, 2σ). One corundum grain is highly 17 O-enriched (δ 17 O ∼ +60 per mille, δ 18 O

  8. Elemental and isotopic (C, O, Sr, Nd) compositions of Late Paleozoic carbonated eclogite and marble from the SW Tianshan UHP belt, NW China: Implications for deep carbon cycle

    Science.gov (United States)

    Zhu, Jianjiang; Zhang, Lifei; Lü, Zeng; Bader, Thomas

    2018-03-01

    Subduction zones are important for understanding of the global carbon cycle from the surface to deep part of the mantle. The processes involved the metamorphism of carbonate-bearing rocks largely control the fate of carbon and contribute to local carbon isotopic heterogeneities of the mantle. In this study, we present petrological and geochemical results for marbles and carbonated eclogites in the Southwestern Tianshan UHP belt, NW China. Marbles are interlayered with coesite-bearing pelitic schists, and have Sr-Nd isotopic values (εNd (T=320Ma) = -3.7 to -8.9, 87Sr/86Sr (i) = 0.7084-0.7089), typical of marine carbonates. The marbles have dispersed low δ18OVSMOW values (ranging from 14 to 29‰) and unaffected carbon isotope (δ13CVPDB = -0.2-3.6‰), possibly due to infiltration of external H2O-rich fluids. Recycling of these marbles into mantle may play a key role in the carbon budget and contributed to the mantle carbon isotope heterogeneity. The carbonated eclogites have high Sr isotopic compositions (87Sr/86Sr (i) = 0.7077-0.7082) and positive εNd (T = 320 Ma) values (from 7.6 to 8.2), indicative of strong seafloor alteration of their protolith. The carbonates in the carbonated eclogites are mainly dolomite (Fe# = 12-43, Fe# = Fe2+/(Fe2+ + Mg)) that were added into oceanic basalts during seafloor alteration and experienced calcite - dolomite - magnesite transformation during the subduction metamorphic process. The uniformly low δ18O values (∼11.44‰) of carbonates in the carbontaed eclogites can be explained by closed-system equilibrium between carbonate and silicate minerals. The low δ13C values (from -3.3 to -7.7‰) of the carbonated eclogites most likely reflect contribution from organic carbon. Recycling of these carbonated eclogites with C isotope similar to typical mantle reservoirs into mantle may have little effect on the mantle carbon isotope heterogeneity.

  9. Magnesium isotopic composition of the mantle

    Science.gov (United States)

    Teng, F.; Li, W.; Ke, S.; Marty, B.; Huang, S.; Dauphas, N.; Wu, F.; Helz, R. L.

    2009-12-01

    Studies of Mg isotopic composition of the Earth not only are important for understanding its geochemistry but also can shed light on the accretion history of the Earth as well as the evolution of the Earth-Moon system. However, to date, the Mg isotopic composition of the Earth is still poorly constrained and highly debated. There is uncertainty in the magnitude of Mg isotope fractionation at mantle temperatures and whether the Earth has a chondritic Mg isotopic composition or not. To constrain further the Mg isotopic composition of the mantle and investigate the behavior of Mg isotopes during igneous differentiation, we report >200 high-precision (δ26Mg French Polynesian volcanoes (Society island and Cook Austral chain); 3) olivine grains from Hawaiian volcanoes (Kilauea, Koolau and Loihi) and 4) peridotite xenoliths from Australia, China, France, Tanzania and USA. Global oceanic basalts and peridotite xenoliths have a limited (<0.2 ‰) variation in Mg isotopic composition, with an average δ26Mg = -0.25 relative to DSM3. Olivines from Hawaiian lavas have δ26Mg ranging from -0.43 to +0.03, with most having compositions identical to basalts and peridotites. Therefore, the mantle’s δ26Mg value is estimated to be ~ -0.25 ± 0.1 (2SD), different from that reported by Wiechert and Halliday (2007; δ26Mg = ~ 0) but similar to more recent studies (δ26Mg = -0.27 to -0.33) (Teng et al. 2007; Handler et al. 2009; Yang et al., 2009). Moreover, we suggest the Earth, as represented by the mantle, has a Mg isotopic composition similar to chondrites (δ26Mg = ~-0.33). The need for a model such as that of Wiechert and Halliday (2007) that involves sorting of chondrules and calcium-aluminum-rich inclusions in the proto planetary disc is thus not required to explain the Mg isotopic composition of the Earth.

  10. The ruthenium isotopic composition of the oceanic mantle

    Science.gov (United States)

    Bermingham, K. R.; Walker, R. J.

    2017-09-01

    The approximately chondritic relative, and comparatively high absolute mantle abundances of the highly siderophile elements (HSE), suggest that their concentrations in the bulk silicate Earth were primarily established during a final ∼0.5 to 1% of ;late accretion; to the mantle, following the cessation of core segregation. Consequently, the isotopic composition of the HSE Ru in the mantle reflects an amalgamation of the isotopic compositions of late accretionary contributions to the silicate portion of the Earth. Among cosmochemical materials, Ru is characterized by considerable mass-independent isotopic variability, making it a powerful genetic tracer of Earth's late accretionary building blocks. To define the Ru isotopic composition of the oceanic mantle, the largest portion of the accessible mantle, we report Ru isotopic data for materials from one Archean and seven Phanerozoic oceanic mantle domains. A sample from a continental lithospheric mantle domain is also examined. All samples have identical Ru isotopic compositions, within analytical uncertainties, indicating that Ru isotopes are well mixed in the oceanic mantle, defining a μ100Ru value of 1.2 ± 7.2 (2SD). The only known meteorites with the same Ru isotopic composition are enstatite chondrites and, when corrected for the effects of cosmic ray exposure, members of the Main Group and sLL subgroup of the IAB iron meteorite complex which have a collective CRE corrected μ100Ru value of 0.9 ± 3.0. This suggests that materials from the region(s) of the solar nebula sampled by these meteorites likely contributed the dominant portion of late accreted materials to Earth's mantle.

  11. Multi-element isotope dilution analyses using ICP-MS

    International Nuclear Information System (INIS)

    Volpe, A.M.

    1996-01-01

    Presently, 37 elements ranging from light (Li,B) through transition metals, noble, rare earth and heavy elements, to actinides and transuranics (Pu, Am, Cm) are measured by isotope dilution at Lawrence Livermore National Laboratory. Projects range from geological and hydrological to biological. The research goal is to measure accurately many elements present in diverse matrices at trace (ppb) levels using isotope dilution methods. Major advantages of isotope dilution methods are accuracy, elimination of ion intensity calibration, and quantitation for samples that require chemical separation. Accuracy depends on tracer isotope calibration, tracer-sample isotopic equilibration, and appropriate background, isobaric and mass bias corrections. Propagation of isotope ratio error due to improper tracer isotope addition is a major concern with multi-element analyses when abundances vary widely. 11 refs., 3 figs

  12. Isotopic composition of past precipitation

    International Nuclear Information System (INIS)

    Edwards, T.W.D.

    1998-01-01

    The distribution of stable isotopes in precipitation provides critical quantitative information about the global water cycle. The first PAGES/IAEA ISOMAP workshop was held at the IAEA headquarters in Vienna, 24-26 August 1998, which gathered 32 participants. The presentation and discussions demonstrated that a high level of sophistication already exists in the development of transfer functions between measured parameters and precipitation, as a result of the extensive use of water isotope tracers in paleo-environmental investigations, but a major challenge facing both producers and users of paleo-isotope data is the effective management of data and meta-data, to permit ready retrieval of raw and inferred data for comparison and reinterpretation. This will be in important goal of future ISOMAP activities. The critical need for more paleo-data from low latitudes was clearly recognized

  13. Elemental composition of cosmic ray

    International Nuclear Information System (INIS)

    Yanagida, Shohei

    1987-01-01

    The report first summarizes some data that have been obtained so far from observation of isotopes and elements in cosmic rays in the low energy region. Then, objectives of studies planned to be carried out with Astromag are outlined and the number of incident particles expected to be measured by baloon observation is estimated. Heavy elements with atomic numbers of greater than 30 are considered to be formed through neutron absorption reactions by the s- or r-process. Observations show that products of the r-process is abundant in cosmic ray sources. The escape length depends on energy. In relation to this, it has been reported that the ratios Ar-Fe and Ca-Fe increase above 200 GeV-n while such a tendency is not observed for K, Sc, Ti or V. Thus, no satisfactory models are available at present which can fully explain the changes in the escape length. The ratio 3 He- 4 He in the range of 5 - 10 GeV-n is inconsistent with the general theory that interprets the escape length of heavy elements. Some models, including the supermetallicity model and Wolf Rayet theory, have been proposed to explain unusual ratios of isotopes in cosmic rays, but more measurements are required to verify them. It is expected that Astromag can serve to make observations that can clarify these points. (Nogami, K.)

  14. Oxygen isotope and trace element compositions of platiniferous dunite pipes of the Bushveld Complex, South Africa - Signals from a recycled mantle component?

    Science.gov (United States)

    Günther, T.; Haase, K. M.; Junge, M.; Oberthür, T.; Woelki, D.; Krumm, S.

    2018-06-01

    Platiniferous dunite pipes occur in the lower mafic/ultramafic portion of the Rustenburg Layered Suite of the Bushveld large igneous province (LIP). Olivine compositions in these pipes range from forsterite (Fo) 80 to 35 mol% and suggest crystallization from variably evolved magmas at high temperatures ( 1200 °C). The most primitive olivines are from a stock unit and have the highest contents of Ni (>0.15 wt%) and lowest contents of Mn (formation of the fayalitic olivines with its high Mn contents (>0.3 wt%). High δ18O values of olivine (5.7-7.0‰) and pyroxene (6.7-7.4‰) are akin to those of the Lower and Critical Zone of the Bushveld intrusion suggesting a common origin. The constant high O isotope ratios with variable Fo contents in the olivines are unlike trends observed in olivine phenocrysts in magmas forming by assimilation-fractional crystallization. We suggest that the high δ18O in the most primitive dunites reflect that of the primary melt of the Bushveld pipes, indicating either a bulk assimilation of crust prior to pipe formation or a contribution from recycled oceanic crust in the sub-continental lithospheric mantle (SCLM). The latter scenario is supported by the high Ni/Mn ratios in primitive pipe olivine that might be inherited from melting of a pyroxene-rich mantle source.

  15. Isotopic anomalies in high Z elements: Uranium?

    International Nuclear Information System (INIS)

    Jovanovic, S.; Reed, G.W. Jr.; Essling, A.M.; Rauh, E.G.; Graczyk, D.G.

    1989-03-01

    Uranium in terrestrial volcanic ejecta from mantle-related sources has been analyzed mass spectrometrically. The objective was to seek supporting evidence for or refutation isotopic variations reported by Fried et al. (1985) for some such samples. The possibility that terrestrial U is not of constant isotopic composition is extraordinary. If true, mechanisms for creating the variation must be sought and the lack of homogenization within the earth addressed. Samples of 100 grams or more were processed in order to minimize reagent and environmental (laboratory) blank interference and to permit isolation of large amounts (several to tens of μg) of U for the mass spectrometer (MS) measurements, which utilizes aliquots of /approximately/1 μg. Aliquants from four volcanic samples gave data which indicate enrichments of 235 U ranging from 0.2% to 5.9% in the 235/238 ratio relative normal uranium ratios. These relative enrichments are consistent with, and in some cases, higher than the 0.18% enrichment reported by Fried et al. (1985) for two volcanic lava samples. However, we were not able to reproduce their results on the Kilauea lava for which they report 0.18% 235 U enrichment. The relative error in our MS ratios is 0.05% -- 0.07%. 1 tab

  16. Spectral determination of thallium isotope composition

    International Nuclear Information System (INIS)

    Polyanskij, V.A.; Turkin, Yu.I.; Yakimova, N.M.

    1986-01-01

    The photoelectric non-standard method for determination of the thallium isotope composition is developed. The analysis is carried out by measuring the brightness of the Hfs components in the line Tl Iλ535.04 nm. The relative standard deviation of the results of the isotope analysis of thallium as metal is 0.02 and of thallium salts - 0.02-0.05

  17. Calcium Isotopic Composition of Bulk Silicate Earth

    Science.gov (United States)

    Kang, J.; Ionov, D. A.; Liu, F.; Zhang, C.; Zhang, Z.; Huang, F.

    2016-12-01

    Ca isotopes are used to study the accretion history of the Earth and terrestrial planets, but, Ca isotopic composition of the Bulk Silicate Earth (BSE) remains poorly constrained [1]. To better understand the Ca isotopic composition of BSE, we analyzed 22 well studied peridotite xenoliths from Tariat (Mongolia), Vitim (southern Siberia) and Udachnaya (Siberian Craton). These samples include both fertile and highly depleted garnet and spinel peridotites that show no or only minor post-melting metasomatism or alteration. Ca isotope measurements were done on a Triton-TIMS using double spike method at the Guangzhou Institute of Geochemistry, CAS. The data are reported as δ44/40Ca (relative to NIST SRM 915a). Results for geostandards are consistent with those from other laboratories. 2 standard deviations of SRM 915a analyses are 0.13‰ (n=48). δ44/40Ca of both and fertile and refractory peridotites range from 0.79 to 1.07‰ producing an average of 0.93±0.12‰ (2SD). This value defines the Ca isotopic composition of the BSE, which is consistent with the average δ44/40Ca of oceanic basalts ( 0.90‰)[2,3]. [1] Huang et al (2010) EPSL 292; [2] Valdes et al (2014) EPSL 394; [3]DePaolo (2004) RMG 55.

  18. Calcium isotopic composition of mantle peridotites

    Science.gov (United States)

    Huang, F.; Kang, J.; Zhang, Z.

    2015-12-01

    Ca isotopes are useful to decipher mantle evolution and the genetic relationship between the Earth and chondrites. It has been observed that Ca isotopes can be fractionated at high temperature [1-2]. However, Ca isotopic composition of the mantle peridotites and fractionation mechanism are still poorly constrained. Here, we report Ca isotope composition of 12 co-existing pyroxene pairs in 10 lherzolites, 1 harzburgite, and 1 wehrlite xenoliths collected from Hainan Island (South Eastern China). Ca isotope data were measured on a Triton-TIMS using the double spike method at the Guangzhou Institute of Geochemistry, CAS. The long-term external error is 0.12‰ (2SD) based on repeated analyses of NIST SRM 915a and geostandards. δ44Ca of clinopyroxenes except that from the wehrlite ranges from 0.85‰ to 1.14‰, while opx yields a wide range from 0.98‰ up to 2.16‰. Co-existing pyroxene pairs show large Δ44Caopx-cpx (defined as δ44Caopx-δ44Cacpx) ranging from 0 to 1.23‰, reflecting equilibrium fractionation controlled by variable Ca contents in the opx. Notably, clinopyroxene of wehrlite shows extremely high δ44Ca (3.22‰). δ44Ca of the bulk lherzolites and harzburgites range from 0.86‰ to 1.14‰. This can be explained by extracting melts with slightly light Ca isotopic compositions. Finally, the high δ44Ca of the wehrlite (3.22‰) may reflect metasomatism by melt which has preferentially lost light Ca isotopes due to chemical diffusion during upwelling through the melt channel. [1] Amini et al (2009) GGR 33; [2] Huang et al (2010) EPSL 292.

  19. Separation of compounds differing in isotopic composition

    International Nuclear Information System (INIS)

    Sievers, R.E.; Brooks, J.J.

    1976-01-01

    Compounds differing in isotopic composition are separated by introducing a mixture of the compounds into a chromatographic column containing a lanthanide chelate as a stationary phase and eluting from the column a fraction which is at least enriched with one of the compounds of the mixture. 17 claims, no drawings

  20. Separation of compounds differing in isotopic composition

    International Nuclear Information System (INIS)

    Sievers, R.E.; Brooks, J.J.

    1975-01-01

    Compounds differing in isotopic composition are separated by introducing a mixture of the compounds into a chromatographic column containing a lanthanide chelate as a stationary phase and eluting from the column a fraction that is at least enriched with one of the compounds of the mixture. (U.S.)

  1. Isotopic compositions of boron in sediments and their implications

    Digital Repository Service at National Institute of Oceanography (India)

    Shirodkar, P.V.; Yingkai, X.

    The abundance and isotopic compositions of boron in sediments from the salt lakes of Qaidam Basin, China have been determined by thermal ionization mass spectrometry of cesium borate. The results show large variations in the isotopic compositions...

  2. Chemical composition of HAL, an isotopically-unusual Allende inclusion

    International Nuclear Information System (INIS)

    Davis, A.M.; Tanaka, T.; Grossman, L.; Lee, T.; Wasserburg, G.J.

    1982-01-01

    Thirty-seven major, minor and trace elements were determined by INAA and RNAA in samples of hibonite, black rim and portions of friable rim from an unusual Allende inclusion, HAL. The peculiar isotopic, mineralogical and textural properties of HAL are accompanied by very unusual trace element abundances. The most striking feature of the chemistry is the virtual absence of Ce from an inclusion otherwise highly enriched in REE compared to C1 chondrites. HAL is also depleted in Sr, Ba, U, V, Ru, Os and Ir, relative to other refractory elements. Of the lithophile elements determined which are normally considered to be refractory in a gas of solar composition, Sr, Ba, Ce, U and V are the most volatile in oxidizing gases. The distribution of REE between hibonite and rims seems to have been established when hibonite and other refractory minerals were removed at slightly different temperatures from a hot, oxidizing gas in which they previously coexisted as separate grains. On the basis of HAL's chemical and isotopic composition, possible locations for the chemical and mass dependent isotopic fractionation are discussed. (author)

  3. Tin isotope fractionation during magmatic processes and the isotope composition of the bulk silicate Earth

    Science.gov (United States)

    Wang, Xueying; Amet, Quentin; Fitoussi, Caroline; Bourdon, Bernard

    2018-05-01

    Tin is a moderately volatile element whose isotope composition can be used to investigate Earth and planet differentiation and the early history of the Solar System. Although the Sn stable isotope composition of several geological and archaeological samples has been reported, there is currently scarce information about the effect of igneous processes on Sn isotopes. In this study, high-precision Sn isotope measurements of peridotites and basalts were obtained by MC-ICP-MS with a double-spike technique. The basalt samples display small variations in δ124/116Sn ranging from -0.01 ± 0.11 to 0.27 ± 0.11‰ (2 s.d.) relative to NIST SRM 3161a standard solution, while peridotites have more dispersed and more negative δ124Sn values ranging from -1.04 ± 0.11 to -0.07 ± 0.11‰ (2 s.d.). Overall, basalts are enriched in heavy Sn isotopes relative to peridotites. In addition, δ124Sn in peridotites become more negative with increasing degrees of melt depletion. These results can be explained by different partitioning behavior of Sn4+ and Sn2+ during partial melting. Sn4+ is overall more incompatible than Sn2+ during partial melting, resulting in Sn4+-rich silicate melt and Sn2+-rich residue. As Sn4+ has been shown experimentally to be enriched in heavy isotopes relative to Sn2+, the effect of melting is to enrich residual peridotites in relatively more compatible Sn2+, which results in isotopically lighter peridotites and isotopically heavier mantle-derived melts. This picture can be disturbed partly by the effect of refertilization. Similarly, the presence of enriched components such as recycled oceanic crust or sediments could explain part of the variations in Sn isotopes in oceanic basalts. The most primitive peridotite analyzed in this study was used for estimating the Sn isotope composition of the BSE, with δ124Sn = -0.08 ± 0.11‰ (2 s.d.) relative to the Sn NIST SRM 3161a standard solution. Altogether, this suggests that Sn isotopes may be a powerful probe of

  4. Ferropericlase inclusions in ultradeep diamonds from Sao Luiz (Brazil): high Li abundances and diverse Li-isotope and trace element compositions suggest an origin from a subduction mélange

    Science.gov (United States)

    Seitz, Hans-Michael; Brey, Gerhard P.; Harris, Jeffrey W.; Durali-Müller, Soodabeh; Ludwig, Thomas; Höfer, Heidi E.

    2018-05-01

    The most remarkable feature of the inclusion suite in ultradeep alluvial and kimberlitic diamonds from Sao Luiz (Juina area in Brazil) is the enormous range in Mg# [100xMg/(Mg + Fe)] of the ferropericlases (fper). The Mg-richer ferropericlases are from the boundary to the lower mantle or from the lower mantle itself when they coexist with ringwoodite or Mg- perovskite (bridgmanite). This, however, is not an explanation for the more Fe-rich members and a lowermost mantle or a "D" layer origin has been proposed for them. Such a suggested ultra-deep origin separates the Fe-rich fper-bearing diamonds from the rest of the Sao Luiz ultradeep diamond inclusion suite, which also contains Ca-rich phases. These are now thought to have an origin in the uppermost lower mantle and in the transition zone and to belong either to a peridotitic or mafic (subducted oceanic crust) protolith lithology. We analysed a new set of more Fe-rich ferropericlase inclusions from 10 Sao Luiz ultradeep alluvial diamonds for their Li isotope composition by solution MC-ICP-MS (multi collector inductively coupled plasma mass spectrometry), their major and minor elements by EPMA (electron probe micro-analyser) and their Li-contents by SIMS (secondary ion mass spectrometry), with the aim to understand the origin of the ferropericlase protoliths. Our new data confirm the wide range of ferropericlase Mg# that were reported before and augment the known lack of correlation between major and minor elements. Four pooled ferropericlase inclusions from four diamonds provided sufficient material to determine for the first time their Li isotope composition, which ranges from δ7Li + 9.6 ‰ to -3.9 ‰. This wide Li isotopic range encompasses that of serpentinized ocean floor peridotites including rodingites and ophicarbonates, fresh and altered MORB (mid ocean ridge basalt), seafloor sediments and of eclogites. This large range in Li isotopic composition, up to 5 times higher than `primitive upper mantle' Li

  5. Investigations on isotopic composition of dusty mist of southern Tajikistan

    International Nuclear Information System (INIS)

    Abdullaev, S.F.; Abdurasulova, N.A.; Maslov, V.A.; Madvaliev, U.; Juraev, A.A.; Davlatshoev, T. S.U.

    2012-01-01

    Atmosphere physics laboratory under S.U. Umarov Physical and Technical Institute Academy of Sciences of the Republic of Tajikistan have carried out investigations on optical and micro physical properties of arid zone aerosols from 1982. Traces of man-made radioactive isotopes were revealed in sands and dust compositions taken in arid zone of Tajikistan during Soviet-American tests on investigation of arid aerosol. Produced result was the basis for further investigation of element composition for dusty haze distributed from south till central part of the country. We investigated samples of soil collected by natural sedimentation along dusty haze distribution and samples of dusty aerosol (in total 80 samples).

  6. Seasonal Cyclicity in Trace Elements and Stable Isotopes of Modern Horse Enamel.

    Directory of Open Access Journals (Sweden)

    Niels J de Winter

    Full Text Available The study of stable isotopes in fossil bioapatite has yielded useful results and has shown that bioapatites are able to faithfully record paleo-environmental and paleo-climatic parameters from archeological to geological timescales. In an effort to establish new proxies for the study of bioapatites, intra-tooth records of enamel carbonate stable isotope ratios from a modern horse are compared with trace element profiles measured using laboratory micro X-Ray Fluorescence scanning. Using known patterns of tooth eruption and the relationship between stable oxygen isotopes and local temperature seasonality, an age model is constructed that links records from six cheek upper right teeth from the second premolar to the third molar. When plotted on this age model, the trace element ratios from horse tooth enamel show a seasonal pattern with a small shift in phase compared to stable oxygen isotope ratios. While stable oxygen and carbon isotopes in tooth enamel are forced respectively by the state of the hydrological cycle and the animal's diet, we argue that the seasonal signal in trace elements reflects seasonal changes in dust intake and diet of the animal. The latter explanation is in agreement with seasonal changes observed in carbon isotopes of the same teeth. This external forcing of trace element composition in mammal tooth enamel implies that trace element ratios may be used as proxies for seasonal changes in paleo-environment and paleo-diet.

  7. Seasonal Cyclicity in Trace Elements and Stable Isotopes of Modern Horse Enamel.

    Science.gov (United States)

    de Winter, Niels J; Snoeck, Christophe; Claeys, Philippe

    2016-01-01

    The study of stable isotopes in fossil bioapatite has yielded useful results and has shown that bioapatites are able to faithfully record paleo-environmental and paleo-climatic parameters from archeological to geological timescales. In an effort to establish new proxies for the study of bioapatites, intra-tooth records of enamel carbonate stable isotope ratios from a modern horse are compared with trace element profiles measured using laboratory micro X-Ray Fluorescence scanning. Using known patterns of tooth eruption and the relationship between stable oxygen isotopes and local temperature seasonality, an age model is constructed that links records from six cheek upper right teeth from the second premolar to the third molar. When plotted on this age model, the trace element ratios from horse tooth enamel show a seasonal pattern with a small shift in phase compared to stable oxygen isotope ratios. While stable oxygen and carbon isotopes in tooth enamel are forced respectively by the state of the hydrological cycle and the animal's diet, we argue that the seasonal signal in trace elements reflects seasonal changes in dust intake and diet of the animal. The latter explanation is in agreement with seasonal changes observed in carbon isotopes of the same teeth. This external forcing of trace element composition in mammal tooth enamel implies that trace element ratios may be used as proxies for seasonal changes in paleo-environment and paleo-diet.

  8. Elemental composition of Malawian rice.

    Science.gov (United States)

    Joy, Edward J M; Louise Ander, E; Broadley, Martin R; Young, Scott D; Chilimba, Allan D C; Hamilton, Elliott M; Watts, Michael J

    2017-08-01

    Widespread potential dietary deficiencies of calcium (Ca), iron (Fe), iodine (I), selenium (Se) and zinc (Zn) have been identified in Malawi. Several deficiencies are likely to be compounded by high phytic acid (PA) consumption. Rice (Oryza sativa) is commonly consumed in some Malawian populations, and its mineral micronutrient content is important for food security. The considerable irrigation requirements and flooded conditions of paddy soils can also introduce or mobilise potentially toxic elements including arsenic (As), cadmium (Cd) and lead (Pb). The aim of this study was to determine the mineral composition of rice sampled from farmers' fields and markets in Malawi. Rice was sampled from 18 extension planning areas across Malawi with 21 white (i.e. polished) and 33 brown samples collected. Elemental composition was determined by inductively coupled plasma-mass spectrometry (ICP-MS). Arsenic speciation was performed using high-performance liquid chromatography (HPLC)-ICP-MS. Concentration of PA was determined using a PA-total phosphorus assay. Median total concentrations (mg kg -1 , dry weight) of elements important for human nutrition in brown and white rice, respectively, were: Ca = 66.5 and 37.8; Cu = 3.65 and 2.49; Fe = 22.1 and 7.2; I = 0.006 and rice samples, respectively, median PA concentrations were 5438 and 1906 mg kg -1 , and median PA:Zn molar ratios were 29 and 13. Concentrations of potentially toxic elements (mg kg -1 , dry weight) in brown and white rice samples, respectively, were: As = 0.030 and 0.006; Cd  ≤ 0.002 and 0.006; Pb = 0.008 and 0.008. Approximately 95 % of As was found to be inorganic As, where this could be quantified. Malawian rice, like the more widely consumed staple grain maize, contains inadequate Ca, I, Se or Zn to meet dietary requirements. Biofortification strategies could significantly increase Se and Zn concentrations and require further investigation. Concentrations of Fe in rice grain varied

  9. THE NITROGEN ISOTOPIC COMPOSITION OF METEORITIC HCN

    Energy Technology Data Exchange (ETDEWEB)

    Pizzarello, Sandra, E-mail: pizzar@asu.edu [Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85018-1604 (United States)

    2014-12-01

    HCN is ubiquitous in extraterrestrial environments and is central to current theories on the origin of early solar system organic compounds such as amino acids. These compounds, observed in carbonaceous meteorites, were likely important in the origin and/or evolution of early life. As part of our attempts to understand the origin(s) of meteoritic CN{sup –}, we have analyzed the {sup 15}N/{sup 14}N isotopic composition of HCN gas released from water extracts of the Murchison meteorite and found its value to be near those of the terrestrial atmosphere. The findings, when evaluated viz-a-viz molecular abundances and isotopic data of meteoritic organic compounds, suggest that HCN formation could have occurred during the protracted water alteration processes known to have affected the mineralogy of many asteroidal bodies during their solar residence. This was an active synthetic stage, which likely involved simple gasses, organic molecules, their presolar precursors, as well as mineral catalysts and would have lead to the formation of molecules of differing isotopic composition, including some with solar values.

  10. Anomalous isotopic composition of cosmic rays

    International Nuclear Information System (INIS)

    Woosley, S.E.; Weaver, T.A.

    1980-01-01

    Recent measurements of nonsolar isotopic patterns for the elements neon and (perhaps) magnesium in cosmic rays are interpreted within current models of stellar nucleosynthesis. One possible explanation is that the stars currently responsible for cosmic-ray synthesis in the Galaxy are typically super-metal-rich by a factor of two to three. Other possibilities include the selective acceleration of certain zones or masses of supernovas or the enhancement of 22 Ne in the interstellar medium by mass loss from red giant stars and planetary nebulas. Measurements of critical isotopic ratios are suggested to aid in distinguishing among the various possibilities. Some of these explanations place significant constraints on the fraction of cosmic ray nuclei that must be fresh supernova debris and the masses of the supernovas involved. 1 figure, 3 tables

  11. Rare earth elements and neodymium isotopes in sedimentary organic matter

    Science.gov (United States)

    Freslon, Nicolas; Bayon, Germain; Toucanne, Samuel; Bermell, Sylvain; Bollinger, Claire; Chéron, Sandrine; Etoubleau, Joel; Germain, Yoan; Khripounoff, Alexis; Ponzevera, Emmanuel; Rouget, Marie-Laure

    2014-09-01

    We report rare earth element (REE) and neodymium (Nd) isotope data for the organic fraction of sediments collected from various depositional environments, i.e. rivers (n = 25), estuaries (n = 18), open-ocean settings (n = 15), and cold seeps (n = 12). Sedimentary organic matter (SOM) was extracted using a mixed hydrogen peroxide/nitric acid solution (20%-H2O2-0.02 M-HNO3), after removal of carbonate and oxy-hydroxide phases with dilute hydrochloric acid (0.25 M-HCl). A series of experimental tests indicate that extraction of sedimentary organic compounds using H2O2 may be complicated occasionally by partial dissolution of sulphide minerals and residual carbonates. However, this contamination is expected to be minor for REE because measured concentrations in H2O2 leachates are about two-orders of magnitude higher than in the above mentioned phases. The mean REE concentrations determined in the H2O2 leachates for samples from rivers, estuaries, coastal seas and open-ocean settings yield relatively similar levels, with ΣREE = 109 ± 86 ppm (mean ± s; n = 58). The organic fractions leached from cold seep sediments display even higher concentration levels (285 ± 150 ppm; mean ± s; n = 12). The H2O2 leachates for most sediments exhibit remarkably similar shale-normalized REE patterns, all characterized by a mid-REE enrichment compared to the other REE. This suggests that the distribution of REE in leached sedimentary organic phases is controlled primarily by biogeochemical processes, rather than by the composition of the source from which they derive (e.g. pore, river or sea-water). The Nd isotopic compositions for organic phases leached from river sediments are very similar to those for the corresponding detrital fractions. In contrast, the SOM extracted from marine sediments display εNd values that typically range between the εNd signatures for terrestrial organic matter (inferred from the analysis of the sedimentary detrital fractions) and marine organic matter

  12. Normal variations in the isotopic composition of metabolically relevant transition metals in human blood

    Science.gov (United States)

    Van Heghe, L.; Cloquet, C.; Vanhaecke, F.

    2012-04-01

    Cu, Fe and Zn are transition metals with great catalytic, structural and regulating importance in the human body. Hence, an aberrant metabolism of these elements can have serious implications on the health of a person. It is assumed that, due to differences in isotope fractionation, the isotopic composition of these elements in whole blood of patients can be different from that in blood of healthy subjects. Therefore, isotopic analysis of the element affected by the disease can be a promising approach for early diagnosis. A method for isotopic analysis of Cu, Fe and Zn in human whole blood was developed. The simultaneous chromatographic isolation of these elements and the conditions for isotope ratio measurement via multi-collector ICP - mass spectrometry (MC-ICP-MS) were optimized. So far, only whole blood of supposedly healthy volunteers (reference population) was analyzed. Results for Fe confirmed the known differences in isotopic composition between male and female blood. It is also shown that other parameters can have influence as well, e.g., the isotopic composition of Zn seems to be governed by the diet.

  13. IR laser enrichment of light elements isotopes - challenges and prospects

    International Nuclear Information System (INIS)

    Parthasarathy, V.

    2002-01-01

    Full text: Infra-red multiple photon dissociation (IR MPD) of poly-atomic molecules has made considerable progress since its discovery in the early seventies. Since the process was found to be isotopically selective; the possibility of laser isotope separation (LIS) created a lot of initial excitement. While the early investigations were concerned with the fundamental dynamics and potential applications of the phenomenon, serious efforts for the isotope enrichment process have been made only during the last decade. These efforts focussed on aspects to improve both the enrichment factor and throughput in various systems. Many research groups have achieved a good measure of success for scaling up the process for various light elements like carbon, oxygen, silicon and sulphur whose isotopes are quite important in medicine and technology. Significant results have been reported especially for the separation of carbon isotopes wherein macroscopic operating scales have been already realised. This talk will give-a summary of our work carried out at BARC and highlight the current efforts for scaling up the process for carbon isotopes enrichment. This would include the design aspects of a large photochemical reactor with multi-pass, refocusing optics for efficient photon utilization. It will also cover the development of a cryogenic distillation set up and a preparative gas chromatograph for a large scale separation and collection of the isotopically enriched photoproduct in the post irradiation stage. Based on the experience gained and infra structure developed, plans are afoot to separate oxygen and sulphur isotopes using a similar approach

  14. Stable-isotope composition of the water of apple juice

    International Nuclear Information System (INIS)

    Bricout, Jacques; Merlivat, Liliane

    1973-01-01

    By deuterium and oxygen 18 analysis, it was shown that apples' water is enriched in heavier isotopes as compared to rain water. The isotopic composition of the water of reconstituted apple juice is closed to the isotopic content of the rain water used for dilution. Thus, deuterium and oxyden 18 analysis allows a good analytical distinction between natural apple juice and reconstituted juices [fr

  15. Heavy element stable isotope ratios. Analytical approaches and applications

    International Nuclear Information System (INIS)

    Tanimizu, Masaharu; Sohrin, Yoshiki; Hirata, Takafumi

    2013-01-01

    Continuous developments in inorganic mass spectrometry techniques, including a combination of an inductively coupled plasma ion source and a magnetic sector-based mass spectrometer equipped with a multiple-collector array, have revolutionized the precision of isotope ratio measurements, and applications of inorganic mass spectrometry for biochemistry, geochemistry, and marine chemistry are beginning to appear on the horizon. Series of pioneering studies have revealed that natural stable isotope fractionations of many elements heavier than S (e.g., Fe, Cu, Zn, Sr, Ce, Nd, Mo, Cd, W, Tl, and U) are common on Earth, and it had been widely recognized that most physicochemical reactions or biochemical processes induce mass-dependent isotope fractionation. The variations in isotope ratios of the heavy elements can provide new insights into past and present biochemical and geochemical processes. To achieve this, the analytical community is actively solving problems such as spectral interference, mass discrimination drift, chemical separation and purification, and reduction of the contamination of analytes. This article describes data calibration and standardization protocols to allow interlaboratory comparisons or to maintain traceability of data, and basic principles of isotope fractionation in nature, together with high-selectivity and high-yield chemical separation and purification techniques for stable isotope studies.

  16. Paradigms in isotope dilution mass spectrometry for elemental speciation analysis

    International Nuclear Information System (INIS)

    Meija, Juris; Mester, Zoltan

    2008-01-01

    Isotope dilution mass spectrometry currently stands out as the method providing results with unchallenged precision and accuracy in elemental speciation. However, recent history of isotope dilution mass spectrometry has shown that the extent to which this primary ratio measurement method can deliver accurate results is still subject of active research. In this review, we will summarize the fundamental prerequisites behind isotope dilution mass spectrometry and discuss their practical limits of validity and effects on the accuracy of the obtained results. This review is not to be viewed as a critique of isotope dilution; rather its purpose is to highlight the lesser studied aspects that will ensure and elevate current supremacy of the results obtained from this method

  17. Chemical composition of HAL, an isotopically-unusual Allende inclusion

    Science.gov (United States)

    Davis, A. M.; Tanaka, T.; Grossman, L.; Lee, T.; Wasserburg, G. J.

    1982-01-01

    Samples of hibonite, black rim, and portions of friable rim from an unusual Allende inclusion, named HAL, were analyzed by INAA and RNAA for 37 major, minor, and trace elements. An unusually low amount of Ce was found in HAL, although it otherwise was highly enriched in REE compared to C1 chondrites. HAL is also depleted in Sr, Ba, U, V, Ru, Os, and Ir relative to other refractory elements. It is concluded that the distribution of REE between hibonite and rims was established when hibonite and other refractory minerals were removed at slightly different temperatures from a hot, oxidizing gas in which they previously coexisted as separate grains. Possible locations for the chemical and mass dependent isotopic fractionation are considered to be in ejecta from the low temperature helium-burning zone of a supernova and in the locally oxidizing environment generated by evaporation of interstellar grains of near-chondritic chemical composition.

  18. Isotopic composition of cellulose from aquatic organisms

    International Nuclear Information System (INIS)

    DeNiro, M.J.; Epstein, S.

    1981-01-01

    The stable isotopic ratios of oxygen, carbon and the non-exchangeable carbon-bound hydrogen of cellulose from marine plants and animals collected in their natural habitats and from freshwater vascular plants grown in the laboratory under controlled conditions were determined. The delta 18 O values of cellulose from all the plants and animals were 27 +- 3 parts per thousand more positive than the delta 18 O values of the waters in which the organisms grew. Temperature had little or no influence on this relationship for three species of freshwater vascular plants that were analyzed. The deltaD values of the non-exchangeable hydrogen of cellulose from different organisms that grew in the same environment differed by large amounts. This difference ranged up to 200 parts per thousand for different species of algae collected at a single site; the corresponding difference for different species of tunicates and vascular plants was 60 and 20 parts per thousand respectively. The deltaD values of cellulose nitrate from different species of freshwater vascular plants grown in water of constant temperature and isotopic composition differed by as much as 60 parts per thousand. The relationship between the deltaD values of the carbon-bound hydrogen of cellulose and the water used in its synthesis displayed a significant temperature dependence for four species of freshwater vascular plants that were analyzed. (author)

  19. Geochemistry of trace elements and Sr- Nd isotopes of foraminifera shell from the Okinawa Trough

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Trace elemental associations and Sr - Nd isotopic compositions are of important to recognition of biogenic material from mixed marine sediments. The foraminifera shell from the Okinawa Trough strongly enrichesSr, P, Mn andBa, enriches Li, U, Th, Sc, Co, Cu, Pb, Zn, Cr, Rb, Y, Sb and light rare earth elements, slightly enriches V, Ga, Zr, Nb, Cd and middle rare earth elements,is short of Mo, In, Sn, Cs, Hf, Ta, W, Ti, Bi and heavy rare earth elements. The mechanism of elemental enrichment in forminifera is the concentrations of trace elements in sea water and selective absorption of trace elements during foraminifera living, as well as the geochemical affinity between major elements and trace elements. The REE (rare earth elements) partition pattern of foraminifera shell of the Okinawa Trough shows enrichment of middle rare earth elements with slightly negative Ce anomaly,which are different from those of foraminifera of the Pacific Ocean. The Sr, Nd isotopic ratios of the Okinawa Trough foraminifera are 0.709 769 and 0.512 162, respectively, which are different not only from those of oceanic water, but also from those of river water of China's Mainland, the former is slightly higher than those of oceanic water, but much lower than those of river water; the latter is slightly lower than those of oceanic water, but higher than those of river water, demonstrating that the Okinawa Trough sea water has been influenced by river water of China's Mainland.

  20. Mercury emissions and stable isotopic compositions at Vulcano Island (Italy)

    Science.gov (United States)

    Zambardi, T.; Sonke, J. E.; Toutain, J. P.; Sortino, F.; Shinohara, H.

    2009-01-01

    Sampling and analyses methods for determining the stable isotopic compositions of Hg in an active volcanic system were tested and optimized at the volcanic complex of Vulcano (Aeolian Islands, Italy). Condensed gaseous fumarole Hg (fum)T, plume gaseous elemental Hg (g)0 and plume particulate Hg (p)II were obtained at fumaroles F0, F5, F11, and FA. The average total Hg emissions, based on Hg T/SO 2 in condensed fumarolic gases and plumes, range from 2.5 to 10.1 kg y - 1 , in agreement with published values [Ferrara, R., Mazzolai, B., Lanzillotta, E., Nucaro, E., Pirrone, N., 2000. Volcanoes as emission sources of atmospheric mercury in the Mediterranean Basin. Sci. Total Environ. 259(1-3), 115-121; Aiuppa, A., Bagnato, E., Witt, M.L.I., Mather, T.A., Parello, F., Pyle, D.M., Martin, R.S., 2007. Real-time simultaneous detection of volcanic Hg and SO 2 at La Fossa Crater, Vulcano (Aeolian Islands, Sicily). Geophys. Res. Lett. 34(L21307).]. Plume Hg (p)II increases with distance from the fumarole vent, at the expense of Hg (g)0 and indicates significant in-plume oxidation and condensation of fumarole Hg (fum)T. Relative to the NIST SRM 3133 Hg standard, the stable isotopic compositions of Hg are δ 202Hg (fum)T = - 0.74‰ ± 0.18 (2SD, n = 4) for condensed gaseous fumarole Hg (fum)T, δ 202Hg (g)0 = - 1.74‰ ± 0.36 (2SD, n = 1) for plume gaseous elemental Hg (g)0 at the F0 fumarole, and δ 202Hg (p)II = - 0.11‰ ± 0.18 (2SD, n = 4) for plume particulate Hg (p)II. The enrichment of Hg (p)II in the heavy isotopes and Hg (g)0 in the light isotopes relative to the total condensed fumarolic Hg (fum)T gas complements the speciation data and demonstrates a gas-particle fractionation occurring after the gas expulsion in ambient T° atmosphere. A first order Rayleigh equilibrium condensation isotope fractionation model yields a fractionation factor α cond-gas of 1.00135 ± 0.00058.

  1. Conceptual model: possible changes of the seawater uranium isotopic composition through time

    Energy Technology Data Exchange (ETDEWEB)

    Nowitzki, Hannah; Frank, Norbert; Fohlmeister, Jens [Universitaet Heidelberg (Germany)

    2015-07-01

    U behaves in seawater like a conservative element. More than 99% of the oceanic U content is {sup 238}U, whereas {sup 234}U is only present in trace amounts. As the residence time of U is significantly longer than the mixing time of the ocean, the ocean is well mixed with respect to U and its isotopic composition (Dunk 2002). Moreover, living corals incorporate U without isotopic fractionation. Therefore, the past seawater isotopic evolution of ({sup 234}U/{sup 238}U) can be accessed via U/Th age-dating of corals and the subsequent calculation of the initial ({sup 234}U/{sup 238}U) value. The isotopic ({sup 234}U/{sup 238}U) composition of seawater during the last 360 ka scatters around the modern seawater value (δ{sup 234}U ∼ (145±15) %, Henderson 2002). As these variations in the δ{sup 234}U value are rather small, a 'constant seawater isotopic composition hypothesis' is often used to validate U/Th ages of fossil corals. However, some authors find that the variability of the isotopic composition exceeds the expected range and suggest that it provides valuable information on variations in continental weathering and global run-off fluctuations or sea-level changes. This work will attempt to compare literature data of the seawater U isotopic composition to the results of a conceptual box-model of the oceanic U budget.

  2. Electromagnetic separator for light and middle isotope elements

    International Nuclear Information System (INIS)

    Bernas, R.

    1952-01-01

    We describe a separator of isotope with a 60 deg magnetic sector that permits, thanks to a process of neutralization of the space charge, to use efficiently intense ion beams. The ion source for solid is essentially constituted by a discharge of hot cathode in a magnetic field and provides an ion beam focused of more than 10 mA. The result of the first separations (Zn, Sb, Hg) indicates that the isotopes of various elements can be obtained in quantities varying from 10 to 100 mg/24 hours. (author) [fr

  3. Method for separating the isotopes of a chemical element

    International Nuclear Information System (INIS)

    Devienne, F.M.

    1977-01-01

    A beam of positive or negative primary ions of at least one compound of a chemical element is accelerated in order to pass through collision boxes placed in series. As a result of inelastic collisions of the ions with the molecules of a neutral target gas within each collision box, a given percentage of primary ions is dissociated into at least two fragments, one of which is a secondary ion in the form of at least two isotopic species. The collision boxes are brought to a potential V 2 so as to trap preferentially one isotopic species which is condensed within each box. 15 claims, 4 figures

  4. The Use of Lead Isotope and Rare Earth Element Geochemistry for Forensic Geographic Provenancing

    Science.gov (United States)

    Carey, A.; Darrah, T.; Harrold, Z.; Prutsman-Pfeiffer, J.; Poreda, R.

    2008-12-01

    Lead isotope and rare earth element composition of modern human bones are analyzed to explore their utility for geographical provenancing. DNA analysis is the standard for identification of individuals. DNA analysis requires a DNA match for comparison. Thus, DNA analysis is of limited use in cases involving unknown remains. Trace elements are incorporated into bones and teeth during biomineralization, recording the characteristics of an individual's geochemical environment. Teeth form during adolescence, recording the geochemical environment of an individual's youth. Bones remodel throughout an individual's lifetime. Bones consist of two types of bone tissue (cortical and trabecular) that remodel at different rates, recording the geochemical environment at the time of biomineralization. Cortical bone tissue, forming the outer surface of bones, is dense, hard tissue that remodels in 25-30 yrs. Conversely, trabecular bone tissue, the inner cavity of bones, is low density, porous and remodels in 2-5 years. Thus, analyzing teeth and both bone tissues allows for the development of a geographical time line capable of tracking immigration patterns through time instead of only an individual's youth. Geochemical isotopic techniques (Sr, O, C, N) have been used for geographical provenancing in physical anthropology. The isotopic values of Sr, C, O, N are predominantly a function of soil compositions in areas where food is grown or water is consumed. Application of these provenancing techniques has become difficult as an individual's diet may reflect the isotopic composition of foods obtained at the local grocer as opposed to local soil compositions. Thus, we explore the use of REEs and Pb isotopes for geographical provenancing. Pb and REEs are likely more reliable indicators of modern geographical location as their composition are high in bio-available sources such as local soils, atmospheric aerosols, and dust as opposed to Sr, C, O, N that are controlled by food and

  5. Carbon and Oxygen isotopic composition in paleoenvironmental determination

    International Nuclear Information System (INIS)

    Silva, J.R.M. da.

    1978-01-01

    This work reports that the carbon and oxygen isotopic composition separate the mollusks from marine environment of the mollusks from continental environment in two groups isotopically different, making the biological control outdone by environment control, in the isotopic fragmentation mechanisms. The patterns from the continental environment are more rich in O 16 than the patterns from marine environments. The C 12 is also more frequent in the mollusks from continental environments. The carbon isotopic composition in paterns from continental environments is situated betwen - 10.31 and - 4,05% and the oxygen isotopic composition is situated between - 6,95 and - 2,41%. To the marine environment patterns the carbon isotopic composition is between - 2,08 and + 2,65% and the oxigen isotopic composition is between - 2,08 and + 0,45%. Was also analysed fossil marine mollusks shells and their isotopic composition permit the formulation of hypothesis about the environment which they lived. (C.D.G.) [pt

  6. Determination of isotopic composition of uranium in microparticles by secondary ion mass spectrometry

    International Nuclear Information System (INIS)

    Veniaminov, N.N.; Kolesnikov, O.N.; Stebel'kov, V.A.

    1992-01-01

    Aerosol particles including uranium in their composition are specific atmospheric polutants. Uranium is used as nuclear fuel in atomic power stations and in spacecraft power units, and also as a component of nuclear warheads. In order to monitor the discharge of uranium-containing aerosol particles to the atmosphere, they must first be identified. As an example, one may cite an investigation of the elemental composition and radioactivity of particles formed in the accident at the Chernobyl atomic power station. One of the most informative indicators of the origin of uranium-containing aerosol particles is the isotopic composition of the uranium. Secondary ion mass spectrometry (SIMS) offers unique possibilities for the measurement of isotope ratios in individual microscopic objects. At the same time, a measurement of isotope ratios of sulfur in microsection of galenite PbS 2 has shown that the application of SIMS for these purposes is seriously limited by the difference in yield of secondary ions for isotopes with different masses. These discrimination effects, in the case of light elements such as boron, may result in distortion of the isotope ratios by several percent. In the case of heavy elements, however, the effect is less significant, amounting to about 0.5% for lead isotopes. 13 refs., 3 figs., 1 tab

  7. Magnesium isotopic composition of the Earth and chondrites

    Science.gov (United States)

    Teng, Fang-Zhen; Li, Wang-Ye; Ke, Shan; Marty, Bernard; Dauphas, Nicolas; Huang, Shichun; Wu, Fu-Yuan; Pourmand, Ali

    2010-07-01

    To constrain further the Mg isotopic composition of the Earth and chondrites, and investigate the behavior of Mg isotopes during planetary formation and magmatic processes, we report high-precision (±0.06‰ on δ 25Mg and ±0.07‰ on δ 26Mg, 2SD) analyses of Mg isotopes for (1) 47 mid-ocean ridge basalts covering global major ridge segments and spanning a broad range in latitudes, geochemical and radiogenic isotopic compositions; (2) 63 ocean island basalts from Hawaii (Kilauea, Koolau and Loihi) and French Polynesia (Society Island and Cook-Austral chain); (3) 29 peridotite xenoliths from Australia, China, France, Tanzania and USA; and (4) 38 carbonaceous, ordinary and enstatite chondrites including 9 chondrite groups (CI, CM, CO, CV, L, LL, H, EH and EL). Oceanic basalts and peridotite xenoliths have similar Mg isotopic compositions, with average values of δ 25Mg = -0.13 ± 0.05 (2SD) and δ 26Mg = -0.26 ± 0.07 (2SD) for global oceanic basalts ( n = 110) and δ 25Mg = -0.13 ± 0.03 (2SD) and δ 26Mg = -0.25 ± 0.04 (2SD) for global peridotite xenoliths ( n = 29). The identical Mg isotopic compositions in oceanic basalts and peridotites suggest that equilibrium Mg isotope fractionation during partial melting of peridotite mantle and magmatic differentiation of basaltic magma is negligible. Thirty-eight chondrites have indistinguishable Mg isotopic compositions, with δ 25Mg = -0.15 ± 0.04 (2SD) and δ 26Mg = -0.28 ± 0.06 (2SD). The constancy of Mg isotopic compositions in all major types of chondrites suggest that primary and secondary processes that affected the chemical and oxygen isotopic compositions of chondrites did not significantly fractionate Mg isotopes. Collectively, the Mg isotopic composition of the Earth's mantle, based on oceanic basalts and peridotites, is estimated to be -0.13 ± 0.04 for δ 25Mg and -0.25 ± 0.07 for δ 26Mg (2SD, n = 139). The Mg isotopic composition of the Earth, as represented by the mantle, is similar to chondrites

  8. Radiochemical search for neutron-rich isotopes of element 107

    International Nuclear Information System (INIS)

    Schaedel, M.

    1987-01-01

    Recent mass calculations have indicated that there is a region of deformed nuclei around neutron number N=162 that is especially stable against spontaneous fission. Barrier heights of about 5 MeV for Z = 107 nuclides can be extrapolated. To search for new, neutron-rich isotopes of element 107 in radiochemical experiments with 254 Es as a target an on-line chemical separation of element 107 (EKA-Rhenium), especially from the actinide elements is needed. An on-line gas-phase chemistry was developed with the homolog Re based on the volatility of the oxide which is transported in an O 2 containing atmosphere along a temperature gradient in a quartz tube and is condensed onto a thin Ta coated Ni-foil. The authors applied this technique in two series of experiments with their rotating wheel on-line gas-phase chemistry apparatus at the 88-inch cyclotron where they irradiated 254 Es as a target with 93 MeV and 96 MeV 16 O ions to search for 266 107. The assignment of the observed alpha events between 8 and 9 MeV to possibly (1) non actinide contaminants like 212 Po, (2) known isotopes of heavy elements like 261 105, or (3) a new isotope will be discussed

  9. Australis: AMS for ultra sensitive trace element and isotopic studies

    Energy Technology Data Exchange (ETDEWEB)

    Sie, S H; Suter, G F [Commonwealth Scientific and Industrial Research Organisation (CSIRO), North Ryde, NSW (Australia). Div. of Exploration Geoscience

    1994-12-31

    The accelerator mass spectrometer (AMS) at the CSIRO HIAF laboratory is being upgraded to enable in-situ measurements of ultratraces and isotopic-ratios in mineralogical applications. The upgraded system will include a microbeam Cs ion source which is designed to produce better than 50 micrometre diameter Cs beam to enable analyses of monomineralic grains. The Cs primary beam will be mass analysed in order to minimize contamination of the sample. The detection system will be upgraded to enable analyses of elements up to U, at 2 MV terminal voltage for charge states 4 and 5. The system will be known as AUSTRALIS: A.M.S. for Ultra Sensitive TRAce eLement and Isotopic Studies. An overview of the system and the anticipated applications in minerals exploration and mining research are presented. 4 refs., 1 fig.

  10. Australis: AMS for ultra sensitive trace element and isotopic studies

    Energy Technology Data Exchange (ETDEWEB)

    Sie, S.H.; Suter, G.F. [Commonwealth Scientific and Industrial Research Organisation (CSIRO), North Ryde, NSW (Australia). Div. of Exploration Geoscience

    1993-12-31

    The accelerator mass spectrometer (AMS) at the CSIRO HIAF laboratory is being upgraded to enable in-situ measurements of ultratraces and isotopic-ratios in mineralogical applications. The upgraded system will include a microbeam Cs ion source which is designed to produce better than 50 micrometre diameter Cs beam to enable analyses of monomineralic grains. The Cs primary beam will be mass analysed in order to minimize contamination of the sample. The detection system will be upgraded to enable analyses of elements up to U, at 2 MV terminal voltage for charge states 4 and 5. The system will be known as AUSTRALIS: A.M.S. for Ultra Sensitive TRAce eLement and Isotopic Studies. An overview of the system and the anticipated applications in minerals exploration and mining research are presented. 4 refs., 1 fig.

  11. Australis: AMS for ultra sensitive trace element and isotopic studies

    International Nuclear Information System (INIS)

    Sie, S.H.; Suter, G.F.

    1993-01-01

    The accelerator mass spectrometer (AMS) at the CSIRO HIAF laboratory is being upgraded to enable in-situ measurements of ultratraces and isotopic-ratios in mineralogical applications. The upgraded system will include a microbeam Cs ion source which is designed to produce better than 50 micrometre diameter Cs beam to enable analyses of monomineralic grains. The Cs primary beam will be mass analysed in order to minimize contamination of the sample. The detection system will be upgraded to enable analyses of elements up to U, at 2 MV terminal voltage for charge states 4 and 5. The system will be known as AUSTRALIS: A.M.S. for Ultra Sensitive TRAce eLement and Isotopic Studies. An overview of the system and the anticipated applications in minerals exploration and mining research are presented. 4 refs., 1 fig

  12. Characterization of the region and year of production of wines by stable isotopes and elemental analyses

    Directory of Open Access Journals (Sweden)

    M. Day

    1995-06-01

    Full Text Available Stable isotope and elemental analyses were applied to the study of wines produced from the Cabernet Franc vine variety cultivated during several years (1982 to 1990 on specific parts of the Saumur-Champigny vineyard dedicated to the « terroir » experiment of INRA. The purpose of this work was to describe the behaviour or 2H, 13C and 18O isotopes in the water and ethanol of wines in terms of the meteorological conditions (temperature, precipitation and insolation which govern vine growing. Since the « terroir » concept involves a synergy between the c1imate and the soil, the distribution of typical metallic elements was also determined by flame and electrothermal ionization atomic absorption. About twenty parcels, carefully described from the geological and pedological point of view were considered in this study which demonstrated the ability of Sr, Al and Rb to discriminate between wines from the same year but grown on adjacent parcels. The content in trace elements of the wines was also shown to be correlated with the geological nature of the soil. As far as stable isotopes are considered, it appears that the climate of the year of production of a given region has a drastic influence on the isotope ratios of water and ethanol of wines and good correlations way be computed between these parameters and temperature and precipitations. From a more basic aspect, it is also shown that the nature of the soil which governs, at least in a part, the water use efficiency of vine, induces typical variations in the isotopic composition of wines. The results of this study demonstrate also the ability of stable isotope and elemental analyses to determine the geographical origin of a wine, and when the region of production is known, to infer the year of production from meteorological data. This method might prove to be an alternative method to radio carbon analysis for the next vintages.

  13. Isotopic and trace element characteristics of rhyolites from the Valles Caldera, New Mexico. Final technical report

    Energy Technology Data Exchange (ETDEWEB)

    Self, S.; Sykes, M.L. [Hawaii Univ., Honolulu, HI (United States). Dept. of Geology and Geophysics; Wolff, J.A. [Texas Univ., Arlington, TX (United States). Dept. of Geology; Skuba, C.E. [McMaster Univ., Hamilton, ON (Canada). Dept. of Geology

    1991-09-01

    This report is a summary of work supported by DOE grant No. DE-FGO5-87ER13795 that was completed or is still in progress. The stated purpose of this grant was to collect geochemical information (trace element, radiogenic isotope and stable oxygen and hydrogen isotope) on samples from core holes VC-I and VC-2a in the Valles caldera in order to establish a consistent detailed intracaldera stratigraphy and relate this to extracaldera volcanic rock units of the Jemez Mountains. Careful stratigraphic control of the intracaldera units is necessary to evaluate models of caldera formation, ignimbrite deposition, and resurgence. Combined stable and radiogenic isotope and trace element data will also provide major insights to petrogenesis of the Bandelier magma system. The composition of non-hydrothermally altered samples from outflow units of the Bandelier Tuff and related volcanics must be known to assess isotopic variations of intracaldera ignimbrite samples. On detailed examination of the VC-2a core samples, it became apparent that hydrothermal alteration is so extensive that no geochemical information useful for stratigraphic fingerprinting or petrogenesis could be obtained, and that correlation with other intracaldera units and extracaldera units must be made on the basis of stratigraphic position and gross lithologic characteristics. Accordingly, we emphasize geochemical data from the extracaldera Bandelier Tuffs and related units which will be useful for comparison with proposed drill hole VC-4 and for any future studies of the region. The stable isotope, radiogenic isotope and trace element data obtained from this project, combined with existing major and trace element data for volcanic rocks from this area, provide an extensive data base essential to future Continental Scientific Drilling Program projects in the Jemez Mountains of New Mexico.

  14. Stable isotopic composition of East African lake waters

    International Nuclear Information System (INIS)

    Odada, E.O.

    2001-01-01

    The investigation of stable isotopic composition of East African lake waters was conducted by scientists from the Department of Geology, University of Nairobi, as part of the International Decade for the East African Lakes (IDEAL) project and in close collaboration with the scientists from Large Lakes Observatory of the University of Minnesota and the Isotope Hydrology Laboratory of the IAEA in Vienna. The Research Contract was part of the IAEA Co-ordinated Research Programme on Isotope Techniques in Lake Dynamics Investigations, and was sponsored by the Agency. Water and grab sediment samples were obtained from East African Lakes during the month of January and February 1994 and July/August 1995. Water samples were analysed for oxygen and deuterium isotopic composition at the IAEA Laboratories in Vienna, Austria. In this final paper we report the results of the study of oxygen and deuterium isotopic composition from the East African lake waters. (author)

  15. Elucidating the formation of terra fuscas using Sr–Nd–Pb isotopes and rare earth elements

    International Nuclear Information System (INIS)

    Hissler, Christophe; Stille, Peter; Juilleret, Jérôme; Iffly, Jean François; Perrone, Thierry; Morvan, Gilles

    2015-01-01

    Highlights: • Geochemical evidences on stabile phase confirm Bajocian marl as terra fusca parent material. • Precipitation/Dissolution of secondary carbonates controls geochemistry of labile phases. • This terra fusca sequence record at least four geological and environmental events. - Abstract: Carbonate weathering mantles, like terra fusca, are common in Europe but their formation and evolution is still badly understood. We propose to combine geological, mineralogical and pedological knowledge with trace element and isotope data of a weathering mantle as a novel approach to understand the evolution of terra fuscas. Sr–Nd–Pb isotopes and rare earth element (REE) contents were analyzed in a cambisol developing on a typical terra fusca on top of a condensed Bajocian limestone-marl succession from the eastern side of the Paris Basin. The isotope data, REE distribution patterns and mass balance calculations suggest that the cambisol mirrors the trace element enrichments present in this carbonate lithology, which are exceptionally high compared to global average carbonate. The deeper soil horizons are strongly enriched not only in REE (ΣREE: 2640 ppm) but also in redox-sensitive elements such as Fe (44 wt.%), V (1000 ppm), Cr (700 ppm), Zn (550 ppm), As (260 ppm), Co (45 ppm) and Cd (2.4 ppm). The trace element distribution patterns of the carbonate bedrock are similar to those of the soil suggesting their close genetic relationships. Sr–Nd–Pb isotope data allow to identify four principal components in the soil: a silicate-rich pool close to the surface, a leachable REE enriched pool at the bottom of the soil profile, the limestone on which the weathering profile developed and an anthropogenic, atmosphere-derived component detected in the soil leachates of the uppermost soil horizon. The leachable phases are mainly secondary carbonate-bearing REE phases such as bastnaesite ((X) Ca(CO 3 ) 2 F) (for X: Ce, La and Nd). The isotope data and trace element

  16. Tracing subduction zone fluid-rock interactions using trace element and Mg-Sr-Nd isotopes

    Science.gov (United States)

    Wang, Shui-Jiong; Teng, Fang-Zhen; Li, Shu-Guang; Zhang, Li-Fei; Du, Jin-Xue; He, Yong-Sheng; Niu, Yaoling

    2017-10-01

    Slab-derived fluids play a key role in mass transfer and elemental/isotopic exchanges in subduction zones. The exhumation of deeply subducted crust is achieved via a subduction channel where fluids from various sources are abundant, and thus the chemical/isotopic compositions of these rocks could have been modified by subduction-zone fluid-rock interactions. Here, we investigate the Mg isotopic systematics of eclogites from southwestern Tianshan, in conjunction with major/trace element and Sr-Nd isotopes, to characterize the source and nature of fluids and to decipher how fluid-rock interactions in subduction channel might influence the Mg isotopic systematics of exhumed eclogites. The eclogites have high LILEs (especially Ba) and Pb, high initial 87Sr/86Sr (up to 0.7117; higher than that of coeval seawater), and varying Ni and Co (mostly lower than those of oceanic basalts), suggesting that these eclogites have interacted with metamorphic fluids mainly released from subducted sediments, with minor contributions from altered oceanic crust or altered abyssal peridotites. The positive correlation between 87Sr/86Sr and Pb* (an index of Pb enrichment; Pb* = 2*PbN/[CeN + PrN]), and the decoupling relationships and bidirectional patterns in 87Sr/86Sr-Rb/Sr, Pb*-Rb/Sr and Pb*-Ba/Pb spaces imply the presence of two compositionally different components for the fluids: one enriched in LILEs, and the other enriched in Pb and 87Sr/86Sr. The systematically heavier Mg isotopic compositions (δ26Mg = - 0.37 to + 0.26) relative to oceanic basalts (- 0.25 ± 0.07) and the roughly negative correlation of δ26Mg with MgO for the southwestern Tianshan eclogites, cannot be explained by inheritance of Mg isotopic signatures from ancient seafloor alteration or prograde metamorphism. Instead, the signatures are most likely produced by fluid-rock interactions during the exhumation of eclogites. The high Rb/Sr and Ba/Pb but low Pb* eclogites generally have high bulk-rock δ26Mg values

  17. Solvent extraction of elemental sulfur from coal and a determination of its source using stable sulfur isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Hackley, K.C.; Buchanan, D.H.; Coombs, K.; Chaven, C.; Kruse, C.W. (Eastern Illinois University, Charleston, IL (USA). Chemistry Dept.)

    1990-01-01

    Hot tetrachloroethene (perchloroethylen PCE) extracts significant amounts of elemental sulfur (S{sup o}) from weathered coals but not from pristine coals. The objective of this study was to determine whether S{sup o} extracted by PCE is an oxidation product of pyrite or whether it originates in some way from unstable, organically-bound sulfur. The isotopic composition of the PCE-extracted S{sup o} was compared to the isotopic compositions of the pyritic and the organic sulfur in a coal. The S{sup o} was shown to have an isotopic signature similar to the pyritic sulfur. Additionally, the isotopic differences observed between the pyritic, S{sup o} and sulfatic sulfur were consistent with bacterial mediated oxidation of sulfide sulfur (pyrite) as the source of both the sulfatic and elemental sulfur. 21 refs., 2 tabs.

  18. Solvent extraction of elemental sulfur from coal and a determination of its source using stable sulfur isotopes

    Science.gov (United States)

    Hackley, Keith C.; Buchanan, D.H.; Coombs, K.; Chaven, C.; Kruse, C.W.

    1990-01-01

    Hot tetrachloroethene (perchloroethylene, PCE) extracts significant amounts of elemental sulfur (So) from weathered coals but not from pristine coals. The objective of this study was to determine whether So extracted by PCE is an oxidation product of pyrite or whether it originates in some way from unstable, organically-bound sulfur. The isotopic composition of the PCE-extracted So was compared to the isotopic compositions of the pyritic and the organic sulfur in a coal. The So was shown to have an isotopic signature similar to the pyritic sulfur. Additionally, the isotopic differences observed between the pyritic, So and sulfatic sulfur were consistent with bacterial mediated oxidation of sulfide sulfur (pyrite) as the source of both the sulfatic and elemental sulfur. ?? 1990.

  19. The isotopic composition of CO in vehicle exhaust

    NARCIS (Netherlands)

    Naus, S.; Röckmann, T.; Popa, M.E.

    2018-01-01

    We investigated the isotopic composition of CO in the exhaust of individual vehicles. Additionally, the CO 2 isotopes, and the CO:CO 2 , CH 4 :CO 2 and H 2 :CO gas ratios were measured. This was done under idling and revving conditions, and for three vehicles in a full driving cycle on a testbench.

  20. Semiempirical method to determine the uranium isotopic compositions

    International Nuclear Information System (INIS)

    Tegas Sutondo

    2008-01-01

    In a nuclear reactor design calculation, some variations of U 235 enrichment are commonly needed. This will affect the isotopic compositions of the 3 main uranium isotopes i.e. U 234 , U 235 and U 238 for the respective enrichment. Due to the limited compositions data available, it is urgent to make an approximate way that can be used to determine the compositions of the 3 isotopes, for the desired enrichments. This paper presents the theoretical background used for constructing a semi empirical formula to estimate the composition of the 3 uranium isotopes as a function of U 235 enrichment, obtained based on the measurement data available. Based on the available data, and the lack of compositions data within the enrichment range between 3.5 % and around 12 %, it is concluded that 2 separate linear equations i.e. for ≤ 3.5 % and ≥ 3.5 % might be needed for U 235 isotope. For the U 234 isotope, a polynomial equation of 4 th order is well suited to be used for the whole range of enrichment between 0.711 % and 20 %, whilst for higher enrichment (> 20 %), a power function seems to give a better approach. The composition of U 238 can then be determined from the U 235 and U 234 composition at the desired enrichment of U 235 . (author)

  1. Electromagnetic separator for light and middle isotope elements; Separateur electromagnetique pour les isotopes d'elements legers et moyens

    Energy Technology Data Exchange (ETDEWEB)

    Bernas, R [Commissariat a l' Energie Atomique, Lab. du Fort de Chatillon, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1952-07-01

    We describe a separator of isotope with a 60 deg magnetic sector that permits, thanks to a process of neutralization of the space charge, to use efficiently intense ion beams. The ion source for solid is essentially constituted by a discharge of hot cathode in a magnetic field and provides an ion beam focused of more than 10 mA. The result of the first separations (Zn, Sb, Hg) indicates that the isotopes of various elements can be obtained in quantities varying from 10 to 100 mg/24 hours. (author) [French] 0n decrit un separateur d'isotope a secteur magnetique de 60 deg qui permet, grace a un procede de neutralisation de la charge d'espace, d'utiliser efficacement des faisceaux d'ions intenses. La source d'ions pour solide est essentiellement constituee par une decharge a cathode chaude dans un champ magnetique et fournit un faisceau d'ion focalises de plus de 10 mA. Le resultat des premieres separations (Zn, Sb, Hg) indique que les isotopes de divers elements peuvent etre obtenus en quantites variant de 10 a 100 mg/24 heures. (auteur)

  2. Experimental study on isotope fractionation of evaporating water of different initial isotopic composition

    International Nuclear Information System (INIS)

    Pooja Devi; Jain, A.K.; Rao, M.S.; Kumar, B.

    2014-01-01

    The studies of evaporative isotopic fractionation in controlled conditions are of particular importance for understanding the mechanism of evaporation fractionation in natural conditions. We present the measurements of the average isotopic fractionation factors during the evaporation of water having different initial isotopic compositions at constant temperature. The results show that the isotopic composition of residual water become more enriched over the time and the initial isotopic composition of evaporating water has considerable effect on the average isotopic fractionation factors. The average isotopic fractionation factors in evaporation of Water A and Water B under the present experimental conditions were found to be 0.9817 ± 0.0044 and 0.9887 ± 0.0031 for oxygen and 0.9178 ± 0.0182 and 0.9437 ± 0.0169 for hydrogen, respectively. The findings of this work should lead to a better understanding and use of stable isotope techniques in isotope hydrology by using a simple technique of evaporation pan. (author)

  3. Isotopic composition of atmospheric moisture from pan water evaporation measurements.

    Science.gov (United States)

    Devi, Pooja; Jain, Ashok Kumar; Rao, M Someshwer; Kumar, Bhishm

    2015-01-01

    A continuous and reliable time series data of the stable isotopic composition of atmospheric moisture is an important requirement for the wider applicability of isotope mass balance methods in atmospheric and water balance studies. This requires routine sampling of atmospheric moisture by an appropriate technique and analysis of moisture for its isotopic composition. We have, therefore, used a much simpler method based on an isotope mass balance approach to derive the isotopic composition of atmospheric moisture using a class-A drying evaporation pan. We have carried out the study by collecting water samples from a class-A drying evaporation pan and also by collecting atmospheric moisture using the cryogenic trap method at the National Institute of Hydrology, Roorkee, India, during a pre-monsoon period. We compared the isotopic composition of atmospheric moisture obtained by using the class-A drying evaporation pan method with the cryogenic trap method. The results obtained from the evaporation pan water compare well with the cryogenic based method. Thus, the study establishes a cost-effective means of maintaining time series data of the isotopic composition of atmospheric moisture at meteorological observatories. The conclusions drawn in the present study are based on experiments conducted at Roorkee, India, and may be examined at other regions for its general applicability.

  4. Carbon isotopic composition of fossil leaves from the Early ...

    Indian Academy of Sciences (India)

    considerable variation in carbon isotopic composition. The Trambau ... One of the most significant changes in the ocean atmosphere .... cryogenic separation of water, CO2 was dynami- .... light condition, nutrients and temperature are low,.

  5. Characters of chlorine isotopic composition in ocean water

    Digital Repository Service at National Institute of Oceanography (India)

    Xiao, Y.; Zhou, Y.; Liu, W.G.; Hong, A.; Wang, Q.; Wang, Y.; Wei, H.; Shirodkar, P.V.

    The chlorine isotopic composition of ocean water was determined using thermal ionization mass spectrometry based on the measurement of Cs sub(2) Cl sup(+) ion. The results show that the sup(37) Cl/ sup(35) Cl ratios are basically homogeneous...

  6. Compilation of minimum and maximum isotope ratios of selected elements in naturally occurring terrestrial materials and reagents

    Science.gov (United States)

    Coplen, T.B.; Hopple, J.A.; Böhlke, J.K.; Peiser, H.S.; Rieder, S.E.; Krouse, H.R.; Rosman, K.J.R.; Ding, T.; Vocke, R.D.; Revesz, K.M.; Lamberty, A.; Taylor, P.; De Bievre, P.

    2002-01-01

    Documented variations in the isotopic compositions of some chemical elements are responsible for expanded uncertainties in the standard atomic weights published by the Commission on Atomic Weights and Isotopic Abundances of the International Union of Pure and Applied Chemistry. This report summarizes reported variations in the isotopic compositions of 20 elements that are due to physical and chemical fractionation processes (not due to radioactive decay) and their effects on the standard atomic weight uncertainties. For 11 of those elements (hydrogen, lithium, boron, carbon, nitrogen, oxygen, silicon, sulfur, chlorine, copper, and selenium), standard atomic weight uncertainties have been assigned values that are substantially larger than analytical uncertainties because of common isotope abundance variations in materials of natural terrestrial origin. For 2 elements (chromium and thallium), recently reported isotope abundance variations potentially are large enough to result in future expansion of their atomic weight uncertainties. For 7 elements (magnesium, calcium, iron, zinc, molybdenum, palladium, and tellurium), documented isotope-abundance variations in materials of natural terrestrial origin are too small to have a significant effect on their standard atomic weight uncertainties. This compilation indicates the extent to which the atomic weight of an element in a given material may differ from the standard atomic weight of the element. For most elements given above, data are graphically illustrated by a diagram in which the materials are specified in the ordinate and the compositional ranges are plotted along the abscissa in scales of (1) atomic weight, (2) mole fraction of a selected isotope, and (3) delta value of a selected isotope ratio. There are no internationally distributed isotopic reference materials for the elements zinc, selenium, molybdenum, palladium, and tellurium. Preparation of such materials will help to make isotope ratio measurements among

  7. The atomic weight and isotopic composition of nitrogen and their variation in nature

    International Nuclear Information System (INIS)

    Holden, N.E.

    1987-01-01

    Two stable isotopes of nitrogen exist in nature, 14 N and 15 N. The less abundant isotope, 15 N, was discovered in 1929 by Naude, who studied the band spectra of nitric oxide, NO. However, the main source of a standard for this element is the air in the atmosphere, which is made up of approximately 78% N 2 . Reviewed in this paper is the measurements of the isotopic composition in air and its variation around the world. Also investigated is the variation of the isotopic composition in the various compounds or sources of nitrogen compared to the value in air. Data on the atomic weight and non-terrestrial data for nitrogen is also reviewed

  8. SEM and elemental analysis of composite resins

    International Nuclear Information System (INIS)

    Hosoda, H.; Yamada, T.; Inokoshi, S.

    1990-01-01

    Twenty-four chemically cured, 21 light-cured anterior, three light-cured anterior/posterior, and 18 light-cured posterior composite resins were examined using scanning electron microscopy, and the elemental composition of their filler particles was analyzed with an energy dispersive electron probe microanalyzer. According to the results obtained, the composite resins were divided into five groups (traditional, microfilled type, submicrofilled type, hybrid type, and semihybrid), with two additional hypothetical categories (microfilled and hybrid). Characteristics of each type were described with clinical indications for selective guidance of respective composite resins for clinical use

  9. Isotopic composition of primary xenon and the fission of Pu-244

    Energy Technology Data Exchange (ETDEWEB)

    Levskii, L K

    1983-05-01

    The hypothesis that the origin of xenon on earth is due to the fission of uranium and/or transuranium elements is examined. The isotopic composition of primary xenon on earth is calculated using a model (Levskii, 1980) of the isotopic composition of rare gases which is based on the hypothesis of the heterogeneity of the isotopic composition of the elements of the solar system. The isotopic composition of fission-produced xenon in the atmosphere and solid earth is determined to correspond to the abundance of xenon isotopes as a result of the spontaneous fission of Pu-244 (half-life of 8.2 x 10 to the 7th years). The amount of fission-produced xenon in the atmosphere is shown to amount to about 30 percent (Xe-136). Under certain conditions, the degree of the degassing of the solid earth for xenon is 25 percent, which corresponds to a ratio of Kr-84/Xe-130 45 for the earth as a whole.

  10. A paired apatite and calcite clumped isotope thermometry approach to estimating Cambro-Ordovician seawater temperatures and isotopic composition

    Science.gov (United States)

    Bergmann, Kristin D.; Finnegan, Seth; Creel, Roger; Eiler, John M.; Hughes, Nigel C.; Popov, Leonid E.; Fischer, Woodward W.

    2018-03-01

    The secular increase in δ18O values of both calcitic and phosphatic marine fossils through early Phanerozoic time suggests either that (1) early Paleozoic surface temperatures were high, in excess of 40 °C (tropical MAT), (2) the δ18O value of seawater has increased by 7-8‰ VSMOW through Paleozoic time, or (3) diagenesis has altered secular trends in early Paleozoic samples. Carbonate clumped isotope analysis, in combination with petrographic and elemental analysis, can deconvolve fluid composition from temperature effects and therefore determine which of these hypotheses best explain the secular δ18O increase. Clumped isotope measurements of a suite of calcitic and phosphatic marine fossils from late Cambrian- to Middle-late Ordovician-aged strata-the first paired fossil study of its kind-document tropical sea surface temperatures near modern temperatures (26-38 °C) and seawater oxygen isotope ratios similar to today's ratios.

  11. Factors controlling stable isotope composition of European precipitation

    International Nuclear Information System (INIS)

    Rozanski, K.; Sonntag, C.; Muennich, K.O.

    1982-01-01

    The seasonal and spatial variations of stable isotope ratios in present day European precipitation are simulated with a simple multibox model of the mean west-east horizontal transport of the atmospheric water vapour across the European continent. Isotope fractionation during the formation of precipitation leads to an increasing depletion of heavy isotopes in the residual air moisture as it moves towards the centre of the continent. This isotopic depletion is partly compensated, particularly in summer, by evapotranspiration, which is assumed to transfer soil water into the atmosphere without isotope fractionation. The model estimates are based on horizontal water vapour flux data, varying seasonally between 88 and 130 kg m -1 s -1 for the Atlantic coast region, and on the monthly precipitation, evapotranspiration and surface air temperature data available for various locations in Europe. Both continental and seasonal temperature effects observed in the stable isotope composition of European precipitation are fairly well reproduced by the model. The calculations show that the isotopic composition of local precipitation is primarily controlled by regional scale processes, i.e. by the water vapour transport patterns into the continent, and by the average precipitation-evapotranspiration history of the air masses precipitating at a given place. Local parameters such as the surface and/or cloud base temperature or the amount of precipitation modify the isotope ratios only slightly. Implications of the model predictions for the interpretation of stable isotope ratios in earlier periods as they are preserved in ice cores and in groundwater are also discussed. (Auth.)

  12. Characterization of frictional melting processes in subduction zone faults by trace element and isotope analyses

    Science.gov (United States)

    Ishikawa, T.; Ujiie, K.

    2017-12-01

    Pseudotachylytes found in exhumed accretionary complexes, which are considered to be formed originally at seismogenic depths, are of great importance for elucidating frictional melting and concomitant dynamic weakening of the fault during earthquake in subduction zones. However, fluid-rich environment of the subduction zone faults tends to cause extensive alteration of the pseudotachylyte glass matrix in later stages, and thus it has been controversial that pseudotachylytes are rarely formed or rarely preserved. Chemical analysis of the fault rocks, especially on fluid-immobile trace elements and isotopes, can be a useful means to identify and quantify the frictional melting occurred in subduction zone faults. In this paper, we report major and trace element and Sr isotope compositions for pseudotachylyte-bearing dark veins and surrounding host rocks from the Mugi area of the Shimanto accretionary complex (Ujiie et al., J. Struct. Geol. 2007). Samples were collected from a rock chip along the microstructure using a micro-drilling technique, and then analyzed by ICP-MS and TIMS. Major element compositions of the dark veins showed a clear shift from the host rock composition toward the illite composition. The dark veins, either unaltered or completely altered, were also characterized by extreme enrichment in some of the trace elements such as Ti, Zr, Nb and Th. These results are consistent with disequilibrium melting of the fault zone. Model calculations revealed that the compositions of the dark veins can be produced by total melting of clay-rich matrix in the source rock, leaving plagioclase and quartz grains almost unmolten. The calculations also showed that the dark veins are far more enriched in melt component than that expected from the source rock compositions, suggesting migration and concentration of frictional melt during the earthquake faulting. Furthermore, Sr isotope data of the dark veins implied the occurrence of frictional melting in multiple stages

  13. Isotope-dilution analyses of the metallic elements

    International Nuclear Information System (INIS)

    Chastagner, P.

    1982-01-01

    The isotope-dilution mass spectroscopy (IDMS) technique has proven to be to be a reliable, versatile analytical tool. Its applications seem to be limited only by the ingenuity of the investigator. Among its advantages are: small sample size; general applicability; precision and accuracy; dynamic range; simplified chemistry; determination is fixed at the time and place of isotopic homogenization. The last listed item is especially important for nuclear safeguards and processes where inventories are critical. IDMS is now a routine analytical technique in geochemical and nuclear laboratories, and in many environmental laboratories. Microgram and nanogram samples are normally used, frequently with automatic mass spectrometers, in many of these routine applications. More advanced techniques permit picogram and sub picogram samples to be analyzed, and spike to sample ratios can range from 1:1 to 1:10 12 with detection limits at attogram levels for some elements. 3 figures, 3 tables

  14. The stable Cr isotopic compositions of chondrites and silicate planetary reservoirs

    Science.gov (United States)

    Schoenberg, Ronny; Merdian, Alexandra; Holmden, Chris; Kleinhanns, Ilka C.; Haßler, Kathrin; Wille, Martin; Reitter, Elmar

    2016-06-01

    The depletion of chromium in Earth's mantle (∼2700 ppm) in comparison to chondrites (∼4400 ppm) indicates significant incorporation of chromium into the core during our planet's metal-silicate differentiation, assuming that there was no significant escape of the moderately volatile element chromium during the accretionary phase of Earth. Stable Cr isotope compositions - expressed as the ‰-difference in 53Cr/52Cr from the terrestrial reference material SRM979 (δ53/52CrSRM979 values) - of planetary silicate reservoirs might thus yield information about the conditions of planetary metal segregation processes when compared to chondrites. The stable Cr isotopic compositions of 7 carbonaceous chondrites, 11 ordinary chondrites, 5 HED achondrites and 2 martian meteorites determined by a double spike MC-ICP-MS method are within uncertainties indistinguishable from each other and from the previously determined δ53/52CrSRM979 value of -0.124 ± 0.101‰ for the igneous silicate Earth. Extensive quality tests support the accuracy of the stable Cr isotope determinations of various meteorites and terrestrial silicates reported here. The uniformity in stable Cr isotope compositions of samples from planetary silicate mantles and undifferentiated meteorites indicates that metal-silicate differentiation of Earth, Mars and the HED parent body did not cause measurable stable Cr isotope fractionation between these two reservoirs. Our results also imply that the accretionary disc, at least in the inner solar system, was homogeneous in its stable Cr isotopic composition and that potential volatility loss of chromium during accretion of the terrestrial planets was not accompanied by measurable stable isotopic fractionation. Small but reproducible variations in δ53/52CrSRM979 values of terrestrial magmatic rocks point to natural stable Cr isotope variations within Earth's silicate reservoirs. Further and more detailed studies are required to investigate whether silicate

  15. Isotopic composition of fission gases in LWR fuel

    International Nuclear Information System (INIS)

    Jonsson, T.

    2000-01-01

    Many fuel rods from power reactors and test reactors have been punctured during past years for determination of fission gas release. In many cases the released gas was also analysed by mass spectrometry. The isotopic composition shows systematic variations between different rods, which are much larger than the uncertainties in the analysis. This paper discusses some possibilities and problems with use of the isotopic composition to decide from which part of the fuel the gas was released. In high burnup fuel from thermal reactors loaded with uranium fuel a significant part of the fissions occur in plutonium isotopes. The ratio Xe/Kr generated in the fuel is strongly dependent on the fissioning species. In addition, the isotopic composition of Kr and Xe shows a well detectable difference between fissions in different fissile nuclides. (author)

  16. Chinese dietary composition and element ingestion

    International Nuclear Information System (INIS)

    Zhu Hongda

    1990-01-01

    Based on the dietary composition and results of some nutrients obtained from the second Nationwide Nutrition Survey in 1982, as well as recently published element contents in various Chinese food, the resultant dietary intake of 19 kinds of elements and 17 radionuclides for Chinese public (mainly for male adults) were estimated. This estimation might be used as basis for development of Chinese Reference Man and estimation of the public background exposure

  17. What Affects the Isotopic Composition of Precipitation - A New Interpretation?

    Energy Technology Data Exchange (ETDEWEB)

    Dody, A. [Nuclear Research Center, Negev, Beer Sheva (Israel)

    2013-07-15

    Rainfall events were sampled in high resolution for stable isotope analyses during four rainy seasons in the central negev of Israel. Each sample is equivalent to 1-2 mm of rain. High variability in the isotopic composition was found in fractions of rain during storms. Two modes of isotopic distribution were found. The first is a wave shaped distribution, where isotopic compositions showed enriched to depleted graded changes and vice versa. The second mode is a step function where each rain cell displayed a constant {delta}{sup 18}O value, but varied greatly from the other rain cells. New interpretation suggests that during the transport of the air parcel system three processes can occur. The first process is a complete blending among the rain cells. The second is a partial isotopic mixing between the rain cells. Finally the third case is when each rain cell maintains its own isotopic values separate from the other rain cells. The third case of no mixing showed unexpected results due to the high air turbulence, vertically and horizontally. There was no evidence of complete mixing among the rain cells of identical air parcel systems. The processes in the air parcel trajectory itself suggested here is put forward as a new way to explain the changes in the isotopic composition during the rain. (author)

  18. Spatiotemporal variation of stable isotopic composition in precipitation

    DEFF Research Database (Denmark)

    Müller, Sascha; Stumpp, Christine; Sørensen, Jens Havskov

    2017-01-01

    influences the isotopic composition at the study site. A simple model of evaporation on falling rain was applied with the aim to reproduce observational data and show the potential influence of changing humidity conditions on precipitation compositions. The rather simple model approach did not fully explain...

  19. Circumstellar and interstellar material in the CO3 chondrite ALHA77307: An isotopic and elemental investigation

    Science.gov (United States)

    Bose, Maitrayee; Floss, Christine; Stadermann, Frank J.; Stroud, Rhonda M.; Speck, Angela K.

    2012-09-01

    We have carried out a NanoSIMS C, N and O ion imaging study of the CO3.0 chondrite ALHA77307. The distribution of O-anomalous grains in ALHA77307 is similar to that observed in other primitive meteorites, and is dominated (84%) by 17O-rich Group 1 grains from low-mass asymptotic giant branch (AGB) stars of close-to-solar metallicity. Four percent of the grains belong to Group 2, whose 18O depletions suggest cool-bottom processing in low-mass stars during the AGB phase, while 8% are Group 4 grains with likely origins in Type II supernova (SN) ejecta. One ferromagnesian silicate has a very high 17O enrichment; nova explosions have been suggested as sources for such grains, but recent models with updated reaction rates show large discrepancies with the grain data, leaving the origins of these grains uncertain. Most of the grains are silicates (86%) with the remainder consisting of oxides (8%), three silica grains and two 'composite' grains composed of multiple subgrains with different elemental compositions. The elemental compositions of the silicates are similar to those found in other studies, with a predominance of non-stoichiometric compositions and high (up to 44 at.%) Fe concentrations. A comparison of isotopic and elemental compositions for all presolar silicates shows that olivine compositions are overabundant in Group 4 grains compared to grains from Groups 1 and 2. This may reflect injection of presolar material from a nearby supernova into the early solar nebula and incorporation into parent bodies before alteration of compositions through irradiation and sputtering in the interstellar medium, as is likely to have occurred for the Group 1 and 2 grains from more distant AGB stars. The matrix material in ALHA77307 contains abundant carbonaceous hotspots with excesses in 15N. However, unlike CR chondrites, the insoluble organic matter (IOM) in ALHA77307 does not have a bulk N isotopic anomaly, consistent with Raman evidence that it has experienced more

  20. Nutritional composition, antinutritional factors and elemental ...

    African Journals Online (AJOL)

    The study is aimed at evaluating nutritional composition, antinutritional factors and elemental analysis of three parts (roots sample RS, seed sample SS and leave sample LS) of Nymphaea lotus (water lily) using standard methods. The plant parts were analyzed for the content of crude lipid, crude fiber, crude proteins, ash, ...

  1. PROXIMATE AND ELEMENTAL COMPOSITION OF WHITE GRUBS

    African Journals Online (AJOL)

    DR. AMINU

    This study determined the proximate and mineral element composition of whole white grubs using standard methods of analysis. ... and 12.75 ± 3.65% respectively. Mineral contents of white grub in terms of relative concentration .... of intracellular Ca, bone mineralization, blood coagulation, and plasma membrane potential ...

  2. The use of trace element data to complement stable isotope methods in the characterization of grape musts

    International Nuclear Information System (INIS)

    Day, M.P.; Zhang, B.L.; Martin, G.J.

    1994-01-01

    Objective physico-chemical methods for the characterization of agricultural produce are important ways of providing impartial information on the composition and origin of food products. Of those techniques successful in this area, stable isotope analyses and especially Site Specific Natural Isotope Fractionation studied by nuclear magnetic resonance (SNIF-NMR) are among the most noteworthy. The use of this technique allows the determination of geographical origin of a variety of finished and raw materials in the food industry. The current capabilities of this technique in the wine industry allow the general area of production to be determined. Trace element concentrations have been analyzed for five regions of France (1989 vintage) in order to improve the accuracy of the SNIF-NMR method. When used in conjunction with stable isotope ratios, the elements Zn, Ca, Sr, and Mg increase the overall classification from 78% (with isotope data only) to 89%. (author)

  3. Natural variations in calcium isotope composition as a monitor of bone mineral balance in humans.

    Science.gov (United States)

    Skulan, J.; Anbar, A.; Thomas, B.; Smith, S.

    2004-12-01

    The skeleton is the largest reservoir of calcium in the human body and is responsible for the short term control of blood levels of this element. Accurate measurement of changes in bone calcium balance is critical to understanding how calcium metabolism responds to physiological and environmental changes and, more specifically, to diagnosing and evaluating the effectiveness of treatments for osteoporosis and other serious calcium-related disorders. It is very difficult to measure bone calcium balance using current techniques, however, because these techniques rely either on separate estimates of bone resorption and formation that are not quantitatively comparable, or on complex and expensive studies of calcium kinetics using administered isotopic tracers. This difficulty is even more apparent and more severe for measurements of short-term changes in bone calcium balance that do not produce detectable changes in bone mineral density. Calcium isotopes may provide a novel means of addressing this problem. The foundation of this isotope application is the ca. 1.3 per mil fractionation of calcium during bone formation, favoring light calcium in the bone. This fractionation results in a steady-state isotopic offset between calcium in bone and calcium in soft tissues, blood and urine. Perturbations to this steady state due to changes in the net formation or resorption of bone should be reflected in changes in the isotopic composition of soft tissues and fluids. Here we present evidence that easily detectable shifts in the natural calcium isotope composition of human urine rapidly reflect changes in bone calcium balance. Urine from subjects in a 17-week bed rest study was analyzed for calcium isotopic composition. Bed rest promotes net resorption of bone, shifting calcium from bone to soft tissues, blood and urine. The calcium isotope composition of patients in this study shifted toward lighter values during bed rest, consistent with net resorption of isotopically

  4. Isotope and trace element models of crustal evolution

    International Nuclear Information System (INIS)

    O'Nions, R.K.; Hamilton, P.J.

    1981-01-01

    Some of the isotopic constraints on the development of continental crust from about 3.8 Ga ago are reviewed. Particularly it is noted that Archaean granitic (sensu lato) rocks have initial 143 Nd/ 144 Nd ratios close to predicted values for the bulk Earth at the time before emplacement, whereas those Phanerozoic granites investigated so far diverge considerably from the bulk Earth and betray the existence of later continental crust in their provenance. Geochemical evidence for recycling of some continent-derived elements into the mantle is examined and the important distinction between selected element recycling and bulk return of continental material is emphasized. Various transport models that have been proposed to model the development of continental crust are examined and some of their differences and similarities, particularly with respect to implications for continental recycling, are highlighted. (author)

  5. Elemental composition of solar energetic particles

    International Nuclear Information System (INIS)

    Cook, W.R. III.

    1981-01-01

    The Low Energy Telescopes on the Voyager spacecraft are used to measure the elemental composition (2 less than or equal to Z less than or equal to 28) and energy spectra (5 to 15 MeV/nucleon) of solar energetic particles (SEPs) in seven large flare events. Four flare events are selected which have SEP abundance ratios approximately independent of energy/nucleon. The abundances for these events are compared from flare to flare and are compared to solar abundances from other sources - spectroscopy of the photosphere and corona, and solar wind measurements. The selected SEP composition results may be described by an average composition plus a systematic flare-to-flare deviation about the average. For each of the four events, the ratios of the SEP abundances to the four-flare average SEP abundances are approximately monotonic functions of nuclear charge Z in the range 6 less than or equal to Z less than or equal to 28. An exception to this Z-dependent trend occurs for He, whose abundance relative to Si is nearly the same in all four events. The four-flare average SEP composition is significantly different from the solar composition determined by photospheric spectroscopy: the elements C, N and O are depleted in SEPs by a factor of about five relative to the elements Na, Mg, Al, Si, Ca, Cr, Fe, and Ni. For some elemental abundance ratios (e.g. Mg/O), the difference between SEP and photospheric results is persistent from flare to flare and is apparently not due to a systematic difference in SEP energy/nucleon spectra between the elements, nor to propagation effects which would result in a time-dependent abundance ratio in individual flare events

  6. Elemental composition of human and animal milk

    International Nuclear Information System (INIS)

    Iyengar, G.V.

    1982-09-01

    A review is presented of the elemental composition of human and animal milk with special reference to trace elements determined through nuclear techniques, particularly neutron activation analysis (NAA). In the joint IAEA/WHO research project, 16 of the 24 elements under investigation have been analysed by NAA with the aid of advanced research nuclear reactors. Literature data are discussed and tabulated in 50 separate tables (one for each element) mainly for the period after 1950. Each table uses a standard format comprising 10 columns indicating (1) source of milk (e.g. human or animal), (2) status of the milk (colostrum, transitional or mature), (3) country of origin, (4) year of data publication, (5) mean concentration, (6) range of single values or standard deviation of the mean, (7) number of samples analysed, (8) analytical technique employed, (9) literature source of the data, and (10) relevant remarks, if any. The most abundant data refer to the minor elements Ca, Cl, K, Mg, N, Na, P and S and to the trace elements Cu, Fe and Zn. Fewer data are available for Cd, Hg, I, Mn, Pb and Se. For the remaining elements, including such biologically important trace elements as As, Co, Cr, F, Mo, Ni, Si and Sn, very few reliable data so far appear to exist

  7. SIMSISH technique does not alter the apparent isotopic composition of bacterial cells.

    Directory of Open Access Journals (Sweden)

    Olivier Chapleur

    Full Text Available In order to identify the function of uncultured microorganisms in their environment, the SIMSISH method, combining in situ hybridization (ISH and nanoscale secondary ion mass spectrometry (nanoSIMS imaging, has been proposed to determine the quantitative uptake of specific labelled substrates by uncultured microbes at the single cell level. This technique requires the hybridization of rRNA targeted halogenated DNA probes on fixed and permeabilized microorganisms. Exogenous atoms are introduced into cells and endogenous atoms removed during the experimental procedures. Consequently differences between the original and the apparent isotopic composition of cells may occur. In the present study, the influence of the experimental procedures of SIMSISH on the isotopic composition of carbon in E. coli cells was evaluated with nanoSIMS and compared to elemental analyser-isotopic ratio mass spectrometer (EA-IRMS measurements. Our results show that fixation and hybridization have a very limited, reproducible and homogeneous influence on the isotopic composition of cells. Thereby, the SIMSISH procedure minimizes the contamination of the sample by exogenous atoms, thus providing a means to detect the phylogenetic identity and to measure precisely the carbon isotopic composition at the single cell level. This technique was successfully applied to a complex sample with double bromine - iodine labelling targeting a large group of bacteria and a specific archaea to evaluate their specific (13C uptake during labelled methanol anaerobic degradation.

  8. SIMSISH Technique Does Not Alter the Apparent Isotopic Composition of Bacterial Cells

    Science.gov (United States)

    Chapleur, Olivier; Wu, Ting-Di; Guerquin-Kern, Jean-Luc; Mazéas, Laurent; Bouchez, Théodore

    2013-01-01

    In order to identify the function of uncultured microorganisms in their environment, the SIMSISH method, combining in situ hybridization (ISH) and nanoscale secondary ion mass spectrometry (nanoSIMS) imaging, has been proposed to determine the quantitative uptake of specific labelled substrates by uncultured microbes at the single cell level. This technique requires the hybridization of rRNA targeted halogenated DNA probes on fixed and permeabilized microorganisms. Exogenous atoms are introduced into cells and endogenous atoms removed during the experimental procedures. Consequently differences between the original and the apparent isotopic composition of cells may occur. In the present study, the influence of the experimental procedures of SIMSISH on the isotopic composition of carbon in E. coli cells was evaluated with nanoSIMS and compared to elemental analyser-isotopic ratio mass spectrometer (EA-IRMS) measurements. Our results show that fixation and hybridization have a very limited, reproducible and homogeneous influence on the isotopic composition of cells. Thereby, the SIMSISH procedure minimizes the contamination of the sample by exogenous atoms, thus providing a means to detect the phylogenetic identity and to measure precisely the carbon isotopic composition at the single cell level. This technique was successfully applied to a complex sample with double bromine – iodine labelling targeting a large group of bacteria and a specific archaea to evaluate their specific 13C uptake during labelled methanol anaerobic degradation. PMID:24204855

  9. Soil Carbon: Compositional and Isotopic Analysis

    Energy Technology Data Exchange (ETDEWEB)

    Moran, James J.; Alexander, M. L.; Laskin, Alexander

    2016-11-01

    This is a short chapter to be included in the next edition of the Encyclopedia of Soil Science. The work here describes techniques being developed at PNNL for investigating organic carbon in soils. Techniques discussed include: laser ablation isotope ratio mass spectrometry, laser ablation aerosol mass spectrometry, and nanospray desorption electrospray ionization mass spectrometry.

  10. Characteristics of stable carbon isotopic composition of shale gas

    Directory of Open Access Journals (Sweden)

    Zhenya Qu

    2016-04-01

    Full Text Available A type Ⅱ kerogen with low thermal maturity was adopted to perform hydrocarbon generation pyrolysis experiments in a vacuum (Micro-Scale Sealed Vessel system at the heating rates of 2 °C/h and 20 °C/h. The stable carbon isotopic compositions of gas hydrocarbons were measured to investigate their evolving characteristics and the possible reasons for isotope reversal. The δ13C values of methane became more negative with the increasing pyrolysis temperatures until it reached the lightest point, after which they became more positive. Meanwhile, the δ13C values of ethane and propane showed a positive trend with elevating pyrolysis temperatures. The carbon isotopic compositions of shale gasses were mainly determined by the type of parent organic matter, thermal evolutionary extent, and gas migration in shale systems. Our experiments and study proved that the isotope reversal shouldn't occur in a pure thermogenic gas reservoir, it must be involved with some other geochemical process/es; although mechanisms responsible for the reversal are still vague. Carbon isotopic composition of the Fayetteville and Barnett shale gas demonstrated that the isotope reversal was likely involved with water–gas reaction and Fischer-Tropsch synthesis during its generation.

  11. The origin of volatile element depletion in early solar system material: Clues from Zn isotopes in chondrules

    Science.gov (United States)

    Pringle, Emily A.; Moynier, Frédéric; Beck, Pierre; Paniello, Randal; Hezel, Dominik C.

    2017-06-01

    Volatile lithophile elements are depleted in the different planetary materials to various degrees, but the origin of these depletions is still debated. Stable isotopes of moderately volatile elements such as Zn can be used to understand the origin of volatile element depletions. Samples with significant volatile element depletions, including the Moon and terrestrial tektites, display heavy Zn isotope compositions (i.e. enrichment of 66Zn vs. 64Zn), consistent with kinetic Zn isotope fractionation during evaporation. However, Luck et al. (2005) found a negative correlation between δ66Zn and 1/[Zn] between CI, CM, CO, and CV chondrites, opposite to what would be expected if evaporation caused the Zn abundance variations among chondrite groups. We have analyzed the Zn isotope composition of multiple samples of the major carbonaceous chondrite classes: CI (1), CM (4), CV (2), CO (4), CB (2), CH (2), CK (4), and CK/CR (1). The bulk chondrites define a negative correlation in a plot of δ66Zn vs 1/[Zn], confirming earlier results that Zn abundance variations among carbonaceous chondrites cannot be explained by evaporation. Exceptions are CB and CH chondrites, which display Zn systematics consistent with a collisional formation mechanism that created enrichment in heavy Zn isotopes relative to the trend defined by CI-CK. We further report Zn isotope analyses of chondrite components, including chondrules from Allende (CV3) and Mokoia (CV3), as well as an aliquot of Allende matrix. All chondrules are enriched in light Zn isotopes (∼500 ppm on 66Zn/64Zn) relative to the bulk, contrary to what would be expected if Zn were depleted during evaporation, on the other hand the matrix has a complementary heavy isotope composition. We report sequential leaching experiments in un-equilibrated ordinary chondrites, which show sulfides are isotopically heavy compared to silicates and the bulk meteorite by ca. +0.65 per mil on 66Zn/64Zn. We suggest isotopically heavy sulfides were

  12. Stable isotope composition of human fingernails from Slovakia

    International Nuclear Information System (INIS)

    Grolmusová, Zuzana; Rapčanová, Anna; Michalko, Juraj; Čech, Peter; Veis, Pavel

    2014-01-01

    Stable isotope composition of human fingernails has proven to be useful for documenting human dietary information and geographical patterns in archeological, forensic, anthropological and biological studies. Therefore, it is of interest to detect all factors influencing the stable isotopic composition in the certain regions in the world. Carbon and nitrogen isotope data of human fingernail keratin from 52 individuals from Slovakia were reported in this study. The online combustion and continuous flow isotope-ratio mass spectrometer Delta V Advantage was used for δ 13 C and δ 15 N analysis of fingernail keratin samples from 24 vegetarian and 28 omnivorous individuals. A group of people with frequent meat consumption showed enrichment in 13 C and 15 N isotopes in fingernails. A similar trend was observed with increasing seafood in an individual's diet. Moreover a significant difference was revealed between smokers and nonsmokers for both δ 13 C and δ 15 N values. These data were compared to previously published δ 13 C and δ 15 N fingernail values from across the globe. This study brings new information on the stable isotope signature of individuals from Slovakia and characterizes the Central European region for the first time. The stable isotope composition of fingernails is influenced by the frequency of meat and seafood consumption as well as smoking. - Highlights: • This study deals with stable isotope analyses of fingernails from Slovak volunteers. • δ 13 C and δ 15 N values of vegetarian and omnivore fingernails were compared. • Influence of sex, diet and smoking was studied

  13. Stable isotope composition of human fingernails from Slovakia

    Energy Technology Data Exchange (ETDEWEB)

    Grolmusová, Zuzana, E-mail: zuzana.grolmusova@geology.sk [Comenius University in Bratislava, Faculty of Mathematics, Physics and Informatics, Department of Experimental Physics, Mlynská dolina F2, 842 48 Bratislava (Slovakia); State Geological Institute of Dionýz Štúr, Laboratory of Isotope Geology, Mlynská dolina 1, 817 04 Bratislava (Slovakia); Rapčanová, Anna [Comenius University in Bratislava, Faculty of Mathematics, Physics and Informatics, Department of Experimental Physics, Mlynská dolina F2, 842 48 Bratislava (Slovakia); Michalko, Juraj; Čech, Peter [State Geological Institute of Dionýz Štúr, Laboratory of Isotope Geology, Mlynská dolina 1, 817 04 Bratislava (Slovakia); Veis, Pavel [Comenius University in Bratislava, Faculty of Mathematics, Physics and Informatics, Department of Experimental Physics, Mlynská dolina F2, 842 48 Bratislava (Slovakia); State Geological Institute of Dionýz Štúr, Laboratory of Isotope Geology, Mlynská dolina 1, 817 04 Bratislava (Slovakia)

    2014-10-15

    Stable isotope composition of human fingernails has proven to be useful for documenting human dietary information and geographical patterns in archeological, forensic, anthropological and biological studies. Therefore, it is of interest to detect all factors influencing the stable isotopic composition in the certain regions in the world. Carbon and nitrogen isotope data of human fingernail keratin from 52 individuals from Slovakia were reported in this study. The online combustion and continuous flow isotope-ratio mass spectrometer Delta V Advantage was used for δ{sup 13}C and δ{sup 15}N analysis of fingernail keratin samples from 24 vegetarian and 28 omnivorous individuals. A group of people with frequent meat consumption showed enrichment in {sup 13}C and {sup 15}N isotopes in fingernails. A similar trend was observed with increasing seafood in an individual's diet. Moreover a significant difference was revealed between smokers and nonsmokers for both δ{sup 13}C and δ{sup 15}N values. These data were compared to previously published δ{sup 13}C and δ{sup 15}N fingernail values from across the globe. This study brings new information on the stable isotope signature of individuals from Slovakia and characterizes the Central European region for the first time. The stable isotope composition of fingernails is influenced by the frequency of meat and seafood consumption as well as smoking. - Highlights: • This study deals with stable isotope analyses of fingernails from Slovak volunteers. • δ{sup 13}C and δ{sup 15}N values of vegetarian and omnivore fingernails were compared. • Influence of sex, diet and smoking was studied.

  14. Elemental and isotopic characterization of Japanese and Philippine polished rice samples using instrumental neutron activation analysis and isotope ratio mass spectrometry

    International Nuclear Information System (INIS)

    Pabroa, Preciosa Corazon B.; Sucgang, Raymond J.; Mendoza, Norman dS.; Ebihara, Mitsuru

    2011-01-01

    Rice is a staple food for most Asian countries such as the Philippines and Japan and as such its elemental and isotopic content are of interest to the consumers. Its elemental content may reflect the macro nutrient reduction during milling or probable toxic elements uptake. Three Japanese and four Philippine polished rice samples in his study mostly came from rice bought from supermarkets.These rice samples were washed, dried and ground to fine powder. Instrumental neutron activation analysis (INAA), a very sensitive non-destructive multi-element analytical technique, was used for the elemental analysis of the samples and isotope-ratio mass spectrometry (IRMS) was used to obtain the isotopic signatures of the samples. Results show that compared with the unpolished rice standard NIES CRM10b, the polished Japanese and Philippine rice sampled show reduced concentrations of elements by as much as 1/3 to 1/10 of Mg, Mn, K and Na. Levels of Ca and Zn are not greatly affected. Arsenic is found in all the Japanese rice tested at an average concentration of 0.103 μg/g and three out of four of the Philippine rice at an average concentration of 0.070 μg/g. Arsenic contamination may have been introduced from the fertilizer used in rice fields. Higher levels of Br are seen in two of the Philippine rice at 14 and 34 μg/g with the most probable source being the pesticide methyl bromide. Isotopic ratio of ae 13 C show signature of a C3 plant with possible narrow distinguishable signature of Japanese rice within -27.5 to -28.5 while Philippine rice within -29 to -30. More rice samples will be analyzed to gain better understanding of isotopic signatures to distinguish inter-varietal and/or geographical differences. Elemental composition of soil samples of rice samples sources will be determined for better understanding of uptake mechanisms. (author)

  15. Investigation of Chemical and Physical Changes to Bioapatite During Fossilization Using Trace Element Geochemistry, Infrared Spectroscopy and Stable Isotopes

    Science.gov (United States)

    Suarez, C. A.; Kohn, M. J.

    2013-12-01

    Bioapatite in the form of vertebrate bone can be used for a wide variety of paleo-proxies, from determination of ancient diet to the isotopic composition of meteoric water. Bioapatite alteration during diagenesis is a constant barrier to the use of fossil bone as a paleo-proxy. To elucidate the physical and chemical alteration of bone apatite during fossilization, we analyzed an assortment of fossil bones of different ages for trace elements, using LA-ICP-MS, stable isotopes, and reflected IR spectroscopy. One set of fossil bones from the Pleistocene of Idaho show a diffusion recrystallization profile, however, rare earth element (REE) profiles indicate diffusion adsorption. This suggests that REE diffusion is controlled by changing (namely decreasing) boundary conditions (i.e. decreasing concentration of REE in surrounding pore fluids). Reflected IR analysis along this concentration profile reveal that areas high in U have lost type A carbonate from the crystal structure in addition to water and organics. Stable isotopic analysis of carbon and oxygen will determine what, if any, change in the isotopic composition of the carbonate component of apatite has occurred do to the diffusion and recrystallization process. Analysis of much older bone from the Cretaceous of China reveal shallow REE and U concentration profiles and very uniform reflected IR spectra with a significant loss of type A carbonate throughout the entire bone cortex. Analysis of stable isotopes through the bone cortex will be compared to the stable isotopes collected from the Pleistocene of Idaho.

  16. Measurement of the isotopic composition of galactic cosmic ray carbon, nitrogen and oxygen

    International Nuclear Information System (INIS)

    Wiedenbeck, M.E.; Greiner, D.E.; Bieser, F.S.; Crawford, H.J.; Heckman, H.H.; Lindstrom, P.J.

    1979-06-01

    The results of an investigation of the isotopic composition of galactic cosmic ray carbon, nitrogen and oxygen (E approx. 80 to 230 MeV/amu) made using the U.C. Berkeley HKH instrument aboard the ISEE-3 spacecraft are reported. The combination of high mass resolution and a large statistical sample makes possible a precise determination of the relative isotopic abundances for these elements. In local interplanetary space we find: 13 C/C = 0.067 +- 0.008, 15 N/N = 0.54 +- 0.03, 17 O/O 18 O/O = 0.019 +- 0.003

  17. Multiple enrichment of the Carpathian-Pannonian mantle: Pb-Sr-Nd isotope and trace element constraints

    Science.gov (United States)

    Rosenbaum, Jeffrey M.; Wilson, Marjorie; Downes, Hilary

    1997-07-01

    Pb isotope compositions of acid-leached clinopyroxene and amphibole mineral separates from spinel peridotite mantle xenoliths entrained in Tertiary-Quaternary alkali basalts from the Carpathian-Pannonian Region of eastern Europe provide important constraints on the processes of metasomatic enrichment of the mantle lithosphere in an extensional tectonic setting associated with recent subduction. Principal component analysis of Pb-Sr-Nd isotope and rare earth element compositions of the pyroxenes is used to identify the geochemical characteristics of the original lithospheric mantle protolith and a spectrum of infiltrating metasomatic agents including subduction-related aqueous fluids and silicate melts derived from a subduction-modified mantle wedge which contains a St. Helena-type (HIMU) plume component. The mantle protolith is highly depleted relative to mid-ocean ridge basalt-source mantle with Pb-Nd-Sr isotope compositions consistent with an ancient depletion event. Silicate melt infiltration into the protolith accounts for the primary variance in the Pb-Sr-Nd isotope compositions of the xenoliths and has locally generated metasomatic amphibole. Infiltration of aqueous fluids has introduced radiogenic Pb and Sr without significantly perturbing the rare earth element signature of the protolith. The Pb isotope compositions of the fluid-modified xenoliths suggest that they reacted with aqueous fluids released from a subduction zone which had equilibrated with sediment derived from an ancient basement terrain. We propose a model for mantle lithosphere evolution consistent with available textural and geochemical data for the xenolith population. The Pb-Sr-Nd isotope compositions of both alkaline mafic magmas and rare, subduction-related, calc-alkaline basaltic andesites from the region provide important constraints for the nature of the asthenospheric mantle wedge and confirm the presence of a HIMU plume component. These silicate melts contribute to the metasomatism

  18. Complete Subsurface Elemental Composition Measurements With PING

    Science.gov (United States)

    Parsons, A. M.

    2012-01-01

    The Probing In situ with Neutrons and Gamma rays (PING) instrument will measure the complete bulk elemental composition of the subsurface of Mars as well as any other solid planetary body. PING can thus be a highly effective tool for both detailed local geochemistry science investigations and precision measurements of Mars subsurface reSOurces in preparation for future human exploration. As such, PING is thus fully capable of meeting a majority of both ncar and far term elements in Challenge #1 presented for this conference. Measuring the ncar subsurface composition of Mars will enable many of the MEPAG science goals and will be key to filling an important Strategic Knowledge Gap with regard to In situ Resources Utilization (ISRU) needs for human exploration. [1, 2] PING will thus fill an important niche in the Mars Exploration Program.

  19. Elemental, stable isotopic and biochemical characterization of soil organic matter alteration across a natural peatland gradient

    Science.gov (United States)

    Cowie, G.; Mowbray, S.; Belyea, L.; Laing, C.; Allton, K.; Abbott, G.; Muhammad, A.

    2010-12-01

    Northern peatlands store around one third of global soil C and thus represent a key reservoir. To elucidate how these systems might respond to climate change, field- and laboratory-based experimental incubation studies are being conducted at sites across a natural peatland gradient in the boreonemoral zone of central Sweden (Ryggmossen). The site comprises four successional stages, from edge to centre; Swamp Forest (SF), Lagg Fen (LF), Bog Margin (BM) and Bog Plateau (BP). The well-preserved succession shows strong decreases in mineral cations and pH, and distinct changes in vegetation and water-table depth. As an underpinning to these experiments, comprehensive characterization of natural soil organic matter (SOM) alteration has been carried out through detailed analyses of vegetation and downcore profiles at contrasting topographic sites (hummock vs hollow) in each of the four locations. As illustrated in Figure 1, while some similarities occur in downcore trends, contrasts are observed in C and N elemental and stable isotopic compositions, between stages and, in some cases, between microtopographic settings. Downcore trends and intersite differences are also observed in biochemical yields and molecular composition (carbohydrates, amino acids, phenols, lipids and D/L amino acid ratios). These reflect SOM decay and alteration combined with the effects of contrasting hydrologic, redox and nutrient regimes and differing vegetation and microbial inputs at each of the study sites. Multivariate analysis is used to to elucidate compositional patterns that characterize and delineate progressive SOM decay, specific vegetation types, and the effects of contrasting environmental conditions at the different sites. Figure 1. A. Organic carbon content (wt %), B. Atomic ratio of organic C to total N, C. Stable C isotopic composition of organic C (d13Corg), and D. Stable N isotopic composition of total nitrogen (d15N), all for core profiles from contrasting settings (hummock and

  20. Influence of chemical structure on carbon isotope composition of lignite

    Science.gov (United States)

    Erdenetsogt, Bat-Orshikh; Lee, Insung; Ko, Yoon-Joo; Mungunchimeg, Batsaikhan

    2017-04-01

    During the last two decades, a number of studies on carbon isotopes in terrestrial organic matter (OM) have been carried out and used to determine changes in paleoatmospheric δ13C value as well as assisting in paleoclimate analysis. Coal is abundant terrestrial OM. However, application of its δ13C value is very limited, because the understanding of changes in isotopic composition during coalification is relatively insufficient. The purpose of this study was to examine the influence of the chemical structure on the carbon isotope composition of lignite. Generally, lignite has more complex chemical structures than other higher rank coal because of the existence of various types of oxygen-containing functional groups that are eliminated at higher rank level. A total of sixteen Lower Cretaceous lignite samples from Baganuur mine (Mongolia) were studied by ultimate, stable carbon isotope and solid-state 13C CP/MAS NMR analyses. The carbon contents of the samples increase with increase in depth, whereas oxygen content decreases continuously. This is undoubtedly due to normal coalification process and also consistent with solid state NMR results. The δ13C values of the samples range from -23.54‰ to -21.34‰ and are enriched in 13C towards the lowermost samples. Based on the deconvolution of the NMR spectra, the ratios between carbons bonded to oxygen (60-90 ppm and 135-220 ppm) over carbons bonded to carbon and hydrogen (0-50 ppm and 90-135 ppm) were calculated for the samples. These correlate well with δ13C values (R2 0.88). The results indicate that the δ13C values of lignite are controlled by two mechanisms: (i) depletion in 13C as a result of loss of isotopically heavy oxygen-bounded carbons and (ii) enrichment in 13C caused by a loss of isotopically light methane from aliphatic and aromatic carbons. At the rank of lignite, coal is enriched in 13C because the amount of isotopically heavy CO2 and CO, released from coal as a result of changes in the chemical

  1. Isotope and minor element geochemistry of high arsenic groundwater from Hangjinhouqi, the Hetao Plain, Inner Mongolia

    International Nuclear Information System (INIS)

    Deng Yamin; Wang Yanxin; Ma Teng

    2009-01-01

    High As groundwater is widely distributed in the northwestern Hetao Plain, an arid region with slow groundwater flow. Arsenic concentration in groundwater ranges from 1 to 1000 μg/L. Most water samples have elevated salinities, with Cl and/or HCO 3 as the dominant anions and Na as the dominant cation. High concentrations of As in shallow aquifers are associated with strongly reducing conditions, as evidenced by high concentrations of dissolved organic C (DOC), NH 4 , dissolved sulfide, arsenite and dissolved CH 4 , and relatively low concentrations of NO 3 - and SO 4 2- . Results of the hydrochemical, and H and O isotope geochemical studies indicate that evapotranspiration is an important process controlling the enrichment of Na and Cl as well as trace elements such as As, B, F and Br in groundwater. In Na-HCO 3 -dominated groundwaters, As, B and F were enriched. Decades of irrigation using Yellow River water has resulted in elevation of the groundwater level, which has accelerated salt accumulation in shallow groundwater and surface soil. In addition, irrigation is responsible for the release of some components from aquifer materials and mixing with saline groundwaters, as indicated by minor element and isotope geochemical data. Used to trace groundwater flow paths, Sr isotope composition also indicates that bedrock weathering is one of the primary sources of As in groundwater in the study area.

  2. Automatic measurement system for light element isotope analysis

    International Nuclear Information System (INIS)

    Satake, Hiroshi; Ikegami, Kouichi.

    1990-01-01

    The automatic measurement system for the light element isotope analysis was developed by installing the specially designed inlet system which was controlled by a computer. The microcomputer system contains specific interface boards for the inlet system and the mass spectrometer, Micromass 602 E. All the components of the inlet and the computer system installed are easily available in Japan. Ten samples can be automatically measured as a maximum of. About 160 minutes are required for 10 measurements of δ 18 O values of CO 2 . Thus four samples can be measured per an hour using this system, while usually three samples for an hour using the manual operation. The automatized analysis system clearly has an advantage over the conventional method. This paper describes the details of this automated system, such as apparatuses used, the control procedure and the correction for reliable measurement. (author)

  3. Isotopic composition and origin of the precipitation in Northern Chile

    International Nuclear Information System (INIS)

    Aravena, R.; Pena, H.; Grilli, A.; Pollastri, A.; Fuenzalida, H.

    1997-01-01

    Full text: A three years isotope data on precipitation collected in northern Chile show a very distinct pattern, with depleted δ 18 and -150/00 observed at high altitude stations, compared to δ 18 0 values ranging between - 10 and -6/00 measured at the lower altitude areas. The depleted δ 0 values observed in the high altitude area, the Altiplano, are related to different processes that affect the air masses as moved from the Atlantic, crossed the Amazon Basin (continental effect), ascend the Andes (altitude effect) and precipitated (convective effect) in the Altiplano. It is postulated that a second source of moisture, associated to air masses from the Pacific, explained the enriched isotopic values observed in the lower altitude areas. Similar isotopic pattern, documented in springs and groundwater, indicates that the rain data presented in this paper is an accurate representation of the long term behavior of the isotopic composition of the rain in northern Chile

  4. Stable isotope composition of cocoa beans of different geographical origin.

    Science.gov (United States)

    Perini, Matteo; Bontempo, Luana; Ziller, Luca; Barbero, Alice; Caligiani, Augusta; Camin, Federica

    2016-09-01

    The isotopic profile (δ(13) C, δ(15) N, δ(18) O, δ(2) H, δ(34) S) was used to characterise a wide selection of cocoa beans from different renowned production areas (Africa, Asia, Central and South America). The factors most influencing the isotopic signatures of cocoa beans were climate and altitude for δ(13) C and the isotopic composition of precipitation water for δ(18) O and δ(2) H, whereas δ(15) N and δ(34) S were primarily affected by geology and fertilisation practises. Multi-isotopic analysis was shown to be sufficiently effective in determining the geographical origin of cocoa beans, and combining it with Canonical Discriminant Analysis led to more than 80% of samples being correctly reclassified. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

  5. What controls the isotopic composition of Greenland surface snow?

    Directory of Open Access Journals (Sweden)

    H. C. Steen-Larsen

    2014-02-01

    Full Text Available Water stable isotopes in Greenland ice core data provide key paleoclimatic information, and have been compared with precipitation isotopic composition simulated by isotopically enabled atmospheric models. However, post-depositional processes linked with snow metamorphism remain poorly documented. For this purpose, monitoring of the isotopic composition (δ18O, δD of near-surface water vapor, precipitation and samples of the top (0.5 cm snow surface has been conducted during two summers (2011–2012 at NEEM, NW Greenland. The samples also include a subset of 17O-excess measurements over 4 days, and the measurements span the 2012 Greenland heat wave. Our observations are consistent with calculations assuming isotopic equilibrium between surface snow and water vapor. We observe a strong correlation between near-surface vapor δ18O and air temperature (0.85 ± 0.11‰ °C−1 (R = 0.76 for 2012. The correlation with air temperature is not observed in precipitation data or surface snow data. Deuterium excess (d-excess is strongly anti-correlated with δ18O with a stronger slope for vapor than for precipitation and snow surface data. During nine 1–5-day periods between precipitation events, our data demonstrate parallel changes of δ18O and d-excess in surface snow and near-surface vapor. The changes in δ18O of the vapor are similar or larger than those of the snow δ18O. It is estimated using the CROCUS snow model that 6 to 20% of the surface snow mass is exchanged with the atmosphere. In our data, the sign of surface snow isotopic changes is not related to the sign or magnitude of sublimation or deposition. Comparisons with atmospheric models show that day-to-day variations in near-surface vapor isotopic composition are driven by synoptic variations and changes in air mass trajectories and distillation histories. We suggest that, in between precipitation events, changes in the surface snow isotopic composition are driven by these changes in near

  6. Measurement of Plutonium Isotopic Composition - MGA

    Energy Technology Data Exchange (ETDEWEB)

    Vo, Duc Ta [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2015-08-21

    In this module, we will use the Canberra InSpector-2000 Multichannel Analyzer with a high-purity germanium detector (HPGe) and the MGA isotopic anlysis software to assay a variety of plutonium samples. The module provides an understanding of the MGA method, its attributes and limitations. You will assess the system performance by measuring a range of materials similar to those you may assay in your work. During the final verification exercise, the results from MGA will be combined with the 240Pueff results from neutron coincidence or multiplicity counters so that measurements of the plutonium mass can be compared with the operator-declared (certified) values.

  7. Oxygen Isotope Composition of Nitrate Produced by Freshwater Nitrification

    Science.gov (United States)

    Boshers, D.; Granger, J.; Bohlke, J. K.

    2016-12-01

    Measurements of the naturally occurring nitrogen and oxygen stable isotope ratios of nitrate (NO3-), δ15N and δ18O, can be used to determine the source, dispersal, and fate of natural and contaminant NO3- in aquatic environments. To this end, it is necessary to know the extent to which NO3- isotopologues are modified by biological reactions, as heavy and light isotopes have different reaction rates. The purpose of this study was to determine the influence of the δ18O of ambient water on the isotope composition of NO3- produced during nitrification, the biological oxidation of ammonium (NH4+) to nitrite (NO2-) and then NO3-, which is poorly constrained in freshwater systems. To determine the δ18O of NO3- produced by nitrification in freshwater, we collected water from a stream in New England, which we amended with NH4+ and with increments of 18O-enriched water, to monitor the isotope composition of NO3- produced by a natural consortium of nitrifiers. Added NH4+ was completely oxidized to NO3- over 26 days. The final δ18O of nitrified NO3- revealed sensitivity to the δ18O of water mediated by (a) isotopic equilibration between water and NO2- and (b) kinetic isotope fractionation during O-atom incorporation from water into NO2- and NO3-. Our results concur with nitrifying culture experiments that have demonstrated analogous sensitivity of the δ18O of nitrified NO3- to equilibrium and kinetic O isotope effects (Buchwald et al. 2012), as well as show that these dynamics need to be considered to interpret NO3- isotope distribution in freshwater environments.

  8. Chemical and isotopic composition of precipitations in Syria

    International Nuclear Information System (INIS)

    Abou Zakhem, B.; Hafez, R.

    2007-05-01

    The objective of this study is to determine isotopic characteristics of precipitation, the climatic and geographical conditions affecting isotopic composition in order to obtain the input function of groundwater to evaluate the water resources.13 meteoric stations were selected in Syria for cumulative monthly rainfall sampling during two hydrological cycles; 1991-1992 and 1992-1993. The chemical and isotopic compositions of monthly precipitation were studied. The winter and spring rainfall isotopic characteristics were determined, in addition to the Syrian meteoric line (SMWL) was estimated with a slope of 6.62 and that of both Syria and Jordan of 6.73. The effect of climatic factors as temperature and relative air humidity on oxygen-18, deuterium and d-excess were studied and it was found that the relationship between temperature and oxygen-18 and deuterium is a positive linear correlation; however, it is a negative correlation with d-excess. The mean seasonal variation amplitude of 18 O was about 6%, and the amount effect on isotopic content of precipitation was studied. The geographic factors and its affect on isotopic contents of precipitation such as altitude were considered, furthermore, the isotopic gradient with altitude was determined for both oxygen-18 and deuterium (-0.14 % and -0.84% /100m respectively). The spatial distribution of oxygen-18, deuterium, tritium and d-excess indicted the effect of mountain chains and gaps between mountains on the isotopic content, the continental effect on tritium build-up by about 33% per 100 Km from the coast. The increase of d-excess values towards the south west proves the eastern Mediterranean climate type over this region.(author)

  9. H-Isotopic Composition of Apatite in Northwest Africa 7034

    Science.gov (United States)

    McCubbin, F. M.; Barnes, J. J.; Santos, A. R.; Boyce, J. W.; Anand, M.; Franchi, I. A.; Agee, C. B.

    2016-01-01

    Northwest Africa (NWA) 7034 and its pairings comprise a regolith breccia with a basaltic bulk composition [1] that yields a better match than any other martian meteorite to estimates of Mars' bulk crust composition [1]. Given the similarities between NWA 7034 and the martian crust, NWA 7034 may represent an important sample for constraining the crustal composition of components that cannot be measured directly by remote sensing. In the present study, we seek to constrain the H isotopic composition of the martian crust using Cl-rich apatite in NWA 7034.

  10. Speciated Elemental and Isotopic Characterization of Atmospheric Aerosols - Recent Advances

    Science.gov (United States)

    Shafer, M.; Majestic, B.; Schauer, J.

    2007-12-01

    Detailed elemental, isotopic, and chemical speciation analysis of aerosol particulate matter (PM) can provide valuable information on PM sources, atmospheric processing, and climate forcing. Certain PM sources may best be resolved using trace metal signatures, and elemental and isotopic fingerprints can supplement and enhance molecular maker analysis of PM for source apportionment modeling. In the search for toxicologically relevant components of PM, health studies are increasingly demanding more comprehensive characterization schemes. It is also clear that total metal analysis is at best a poor surrogate for the bioavailable component, and analytical techniques that address the labile component or specific chemical species are needed. Recent sampling and analytical developments advanced by the project team have facilitated comprehensive characterization of even very small masses of atmospheric PM. Historically; this level of detail was rarely achieved due to limitations in analytical sensitivity and a lack of awareness concerning the potential for contamination. These advances have enabled the coupling of advanced chemical characterization to vital field sampling approaches that typically supply only very limited PM mass; e.g. (1) particle size-resolved sampling; (2) personal sampler collections; and (3) fine temporal scale sampling. The analytical tools that our research group is applying include: (1) sector field (high-resolution-HR) ICP-MS, (2) liquid waveguide long-path spectrophotometry (LWG-LPS), and (3) synchrotron x-ray absorption spectroscopy (sXAS). When coupled with an efficient and validated solubilization method, the HR-ICP-MS can provide quantitative elemental information on over 50 elements in microgram quantities of PM. The high mass resolution and enhanced signal-to-noise of HR-ICP-MS significantly advance data quality and quantity over that possible with traditional quadrupole ICP-MS. The LWG-LPS system enables an assessment of the soluble

  11. petrography, compositional characteristics and stable isotope

    African Journals Online (AJOL)

    PROF EKWUEME

    African and South American lithospheric plates (Burke et al., 1971). The basin ...... Tectonic evolution Cretaceous stratigraphy of the. Dahomey Basin.Journal of Mining and Geology, ... theory and application of trace element technique.

  12. Determination of hydrogen isotope composition in organic compounds

    International Nuclear Information System (INIS)

    Ordzhonikidze, K.G.; Parulava, L.P.; Vakhaniya, G.V.; Tarielashvili, V.O.

    1989-01-01

    method for determination of hydrogen isotope composition just in organic compounds using mass-spectrometer of the second class is suggested. The method enables to determine atomic fraction of hydrogen without multiplet separation. The accuracy of determination of deuterium atomic fraction in acetone in 1-99% range was equal to 3-0.2% respectively

  13. Stable isotope compositions of organic carbon and contents of ...

    African Journals Online (AJOL)

    The stable isotope compositions of organic carbon (OC), and contents of OC and nitrogen for four sediment cores recovered from lakes Makat (located in the Ngorongoro Crater), Ndutu and Masek (located in the Serengeti Plains) are used to document sources of organic matter (OM) and climatic changes in sub-arid ...

  14. Finite element modelling of composite castellated beam

    Directory of Open Access Journals (Sweden)

    Frans Richard

    2017-01-01

    Full Text Available Nowadays, castellated beam becomes popular in building structural as beam members. This is due to several advantages of castellated beam such as increased depth without any additional mass, passing the underfloor service ducts without changing of story elevation. However, the presence of holes can develop various local effects such as local buckling, lateral torsional buckling caused by compression force at the flange section of the steel beam. Many studies have investigated the failure mechanism of castellated beam and one technique which can prevent the beam fall into local failure is the use of reinforced concrete slab as lateral support on castellated beam, so called composite castellated beam. Besides of preventing the local failure of castellated beam, the concrete slab can increase the plasticity moment of the composite castellated beam section which can deliver into increasing the ultimate load of the beam. The aim of this numerical studies of composite castellated beam on certain loading condition (monotonic quasi-static loading. ABAQUS was used for finite element modelling purpose and compared with the experimental test for checking the reliability of the model. The result shows that the ultimate load of the composite castellated beam reached 6.24 times than the ultimate load of the solid I beam and 1.2 times compared the composite beam.

  15. Iron isotope composition of particles produced by UV-femtosecond laser ablation of natural oxides, sulfides, and carbonates.

    Science.gov (United States)

    d'Abzac, Francois-Xavier; Beard, Brian L; Czaja, Andrew D; Konishi, Hiromi; Schauer, James J; Johnson, Clark M

    2013-12-17

    The need for femtosecond laser ablation (fs-LA) systems coupled to MC-ICP-MS to accurately perform in situ stable isotope analyses remains an open question, because of the lack of knowledge concerning ablation-related isotopic fractionation in this regime. We report the first iron isotope analysis of size-resolved, laser-induced particles of natural magnetite, siderite, pyrrhotite, and pyrite, collected through cascade impaction, followed by analysis by solution nebulization MC-ICP-MS, as well as imaging using electron microscopy. Iron mass distributions are independent of mineralogy, and particle morphology includes both spheres and agglomerates for all ablated phases. X-ray spectroscopy shows elemental fractionation in siderite (C-rich agglomerates) and pyrrhotite/pyrite (S-rich spheres). We find an increase in (56)Fe/(54)Fe ratios of +2‰, +1.2‰, and +0.8‰ with increasing particle size for magnetite, siderite, and pyrrhotite, respectively. Fe isotope differences in size-sorted aerosols from pyrite ablation are not analytically resolvable. Experimental data are discussed using models of particles generation by Hergenröder and elemental/isotopic fractionation by Richter. We interpret the isotopic fractionation to be related to the iron condensation time scale, dependent on its saturation in the gas phase, as a function of mineral composition. Despite the isotopic variations across aerosol size fractions, total aerosol composition, as calculated from mass balance, confirms that fs-LA produces a stoichiometric sampling in terms of isotopic composition. Specifically, both elemental and isotopic fractionation are produced by particle generation processes and not by femtosecond laser-matter interactions. These results provide critical insights into the analytical requirements for laser-ablation-based stable isotope measurements of high-precision and accuracy in geological samples, including the importance of quantitative aerosol transport to the ICP.

  16. Rare earth element concentrations and Nd isotopes in the Southeast Pacific Ocean

    Science.gov (United States)

    Jeandel, C.; Delattre, H.; Grenier, M.; Pradoux, C.; Lacan, F.

    2013-02-01

    vertical profiles of rare earth element concentrations and Nd isotopic compositions have been measured in the remote southeast Pacific Ocean. The three stations represent contrasting environments: the oligotrophic center of the gyre (station GYR), the "transition zone" east of the South Tropical Front (station EGY), and the Peru-Chile upwelling marked by a pronounced oxygen minimum (station UPX). Rare earth concentrations display nutrient like vertical profiles except at UPX where surface waters are enriched. At this station Nd isotopic compositions are clearly more radiogenic than in the open ocean, suggesting that boundary exchange process is releasing lithogenic rare earth element from the volcanic Andes. Unexpected radiogenic values (ɛNd reaching -3.7) are also observed at 2000 m at station GYR in the Upper Circumpolar Deep Water that commonly have ɛNd values around -6. Exchange processes related to hydrothermal activity are suspected to produce this increase in ɛNd in the vicinity of the East Pacific Rise. These results provide some guidance for higher resolution studies planned in this region by the international GEOTRACES program.

  17. Composition containing transuranic elements for use in the homeopathic treatment of aids

    International Nuclear Information System (INIS)

    Lustig, D.

    1996-01-01

    A homeopathic remedy consisting of a composition containing one or more transuranic elements, particularly plutonium, for preventing and treating acquired immunodeficiency syndrome (AIDS) in humans, as well as seropositivity for human immunodeficiency virus (HIV). Said composition is characterized in that it uses any chemical or isotopic form of one or more transuranic elements (neptunium, plutonium, americium, curium, berkelium, californium or einsteinium), particularly plutonium, said form being diluted and dynamized according to conventional homeopathic methods, particularly the so-called Hahnemann and Korsakov methods, and provided preferably but not exclusively in the form of lactose and/or saccharose globules or granules impregnated with the active principle of said composition. (author)

  18. Isotope composition and volume of Earth's early oceans.

    Science.gov (United States)

    Pope, Emily C; Bird, Dennis K; Rosing, Minik T

    2012-03-20

    Oxygen and hydrogen isotope compositions of Earth's seawater are controlled by volatile fluxes among mantle, lithospheric (oceanic and continental crust), and atmospheric reservoirs. Throughout geologic time the oxygen mass budget was likely conserved within these Earth system reservoirs, but hydrogen's was not, as it can escape to space. Isotopic properties of serpentine from the approximately 3.8 Ga Isua Supracrustal Belt in West Greenland are used to characterize hydrogen and oxygen isotope compositions of ancient seawater. Archaean oceans were depleted in deuterium [expressed as δD relative to Vienna standard mean ocean water (VSMOW)] by at most 25 ± 5‰, but oxygen isotope ratios were comparable to modern oceans. Mass balance of the global hydrogen budget constrains the contribution of continental growth and planetary hydrogen loss to the secular evolution of hydrogen isotope ratios in Earth's oceans. Our calculations predict that the oceans of early Earth were up to 26% more voluminous, and atmospheric CH(4) and CO(2) concentrations determined from limits on hydrogen escape to space are consistent with clement conditions on Archaean Earth.

  19. Hydrogen-isotopic composition of some hydrous manganese minerals

    International Nuclear Information System (INIS)

    Hariya, Y.; Tsutsumi, M.

    1981-01-01

    Initial data on the hydrogen-isotopic compositions in hydrous Mn minerals from various occurrences fall in a wide range from -298 to -84per thousand, relative to SMOW. deltaD-values of todorokite and cryptomelane from Tertiary deposits show -89 and -150per thousand. 10 A-manganite and delta-MnO 2 from deep-sea nodules have relatively restricted deltaD-values ranging from -96 to -84per thousand. The deltaD-values for manganese bog ores from recent hot springs show almost -105per thousand. It is recognized that the isotopic values obtained for the deep-sea nodules and recent bog ores are slightly different ranged. Manganite and groutite are unique in their hydrogen-isotopic compositions, having the most depleted deltaD-values ranging from -298 to -236per thousand. MnO(OH) minerals are more deuterium-depleted hydrous minerals than any other hydrothermal minerals from various ore deposits. Hydrogen-isotope fractionation factors between manganite and water were experimentally determined to be 0.7894, 0.7958 and 0.8078 at 150 0 , 200 0 and 250 0 C respectively. The present experimental results indicate that if manganites were formed at temperatures below 250 0 C, under isotopic equilibrium conditions most of the manganite mineralization in the Tertiary manganese deposits must have precipitated from meteoric hydrothermal solutions. (Auth.)

  20. Sr - an element shows the way - Applications of Sr isotopes for provenance, tracing and migration (Invited)

    Science.gov (United States)

    Prohaska, T.; Irrgeher, J.; Zitek, A.; Teschler Nicola, M.

    2010-12-01

    Strontium - named after the small Scottish town Strontian - as such is an element with little popularity. Firstly described by Martin Heinrich Klaproth in 1798, the metal is used in metallurgy to some extent whereas its compounds are interesting in glass industries, electronics and pyrotechnics. The element has chemical similarity to Ca and makes up 1/60 of the earth’s amount of the latter. Nonetheless, it is its isotopic composition which makes Sr so interesting for a large number of scientists. The natural composition of the four naturally occurring isotopes (84Sr, 86Sr 87Sr and 88Sr) varies in nature due to the radioactive decay of 87Rb to 87Sr. Thus, it was early recognized as geochronometer especially in Ca rich matrices. With increasing precision of applied methodology, the natural variation of the 87Sr/86Sr isotope ratio (analyzed at first mainly by thermal ionization mass spectrometry (TIMS)) became more and more popular in provenance studies. The natural variation of the ratio is mainly determined by the geological age and the original composition of the rock and can be used therefore as fingerprint of the local geology. The ratio is transferred with no significant fractionation via the water into plants and finally via the food chain into animal and human tissues (especially bones and teeth). As the element is chemically similar to Ca, it appears in most matrices. The use for provenance studies is supported by the fact that the long half life (4.8 x 1010 years) does not lead to an alteration during the time scales which are investigated (from recent samples to human or animal skeletal remains which date back up to 30.000 BC). The uniqueness of the system besides the natural variation is defined by the ubiquity in nature and the relatively high (and thus measurable) elemental concentration in most tissues. It was finally the advent of multiple collector inductively coupled plasma mass spectrometry (MC-ICP-MS) which augmented the number of applications

  1. Biosynthetic effects on the stable carbon isotopic compositions of agal lipids: Implications for deciphering the carbon isotopic biomarker record

    NARCIS (Netherlands)

    Sinninghe Damsté, J.S.; Schouten, S.; Klein Breteler, W.C.M.; Blokker, P.; Schogt, N.; Rijpstra, W.I.C.; Grice, K.; Baas, M.

    1998-01-01

    Thirteen species of algae covering an extensive range of classes were cultured and stable carbon isotopic compositions of their lipids were analysed in order to assess carbon isotopic fractionation effects during their biosynthesis. The fatty acids were found to have similar stable carbon isotopic

  2. Chemical and isotopic composition of precipitations in Syria

    International Nuclear Information System (INIS)

    Abou Zakhem, B.; Hafez, R.

    2008-01-01

    13 meteoric stations were selected in syria for cumulative monthly rainfall sampling during two hydrological cycles; 1991-1992 and 1992-1993. The chemical and isotopic compositions of monthly precipitation were studied. The winter and spring rainfall isotopic characteristics were determined, in addition to the syrian or local meteoric line (SMWL) was estimated with a slope of 6.63 and that of both syria and Jordan of 6.73. The effect of climatic factors as temperature and relative air humidity on oxygen-18, deuterium and d-excess were studied and it was found that the relationship between temperature and oxygen-18 and deuterium is a positive linear correlation; however, it is a negative correlation with d-excess. The mean seasonal variation amplitude was determined by 6%, and the amount effect on isotopic content of precipitation was studied. The geographic factors and its affect on isotopic contents of precipitation such as altitude were considered, furthermore, the isotopic gradient with altitude was determined for both oxygen-18 and deuterium (-0.14% and - 0.84%/100 m elevation respectively). The spatial variability of oxygen-18, deuterium, tritium and d-excess indicted the effect of mountain chains and gaps between mountains on the isotopic content of precipitation, the continental effect on tritium build-up by about 33% per 100 Km from the coast. The increase of d-excess values towards the south west proves the eastern mediterranean climate type over this region. (author)

  3. Effects of diagenesis on strontium, carbon, nitrogen and oxygen concentration and isotopic composition of bone

    Science.gov (United States)

    Nelson, Bruce K.; Deniro, Michael J.; Schoeninger, Margaret J.; De Paolo, Donald J.; Hare, P. E.

    1986-09-01

    Paleodietary analysis based on variations in the trace element and stable isotopic composition of inorganic and organic phases in fossil bone depends on the assumption that measured values reflect in vivo values. To test for postmortem alteration, we measured 87Sr /86Sr , 13C /12C , 18O /16O and 15N /14N ratios and Sr concentrations in modern and prehistoric (610 to 5470 yr old) bones of animals with marine or terrestrial diets from Greenland. Bones from modern terrestrial feeders have substantially lower Sr concentrations and more radiogenic 87Sr /86Sr ratios than those from modern marine feeders. This contrast was not preserved in the prehistoric samples, which showed almost complete overlap for both Sr concentration and isotopic composition in bones from the two types of animals. Leaching experiments, X-ray diffraction analysis and infrared spectroscopy indicate that alteration of the Sr concentration and isotopic composition in prehistoric bone probably results from nearly complete exchange with groundwater. Oxygen isotope ratios in fossil apatite carbonate also failed to preserve the original discrimination between modern terrestrial and marine feeders. The C isotope ratio of apatite carbonate did not discriminate between animals with marine or terrestrial diets in the modern samples. Even so, the ranges of apatite δ 13C values in prehistoric bone are more scattered than in modern samples for both groups, suggesting alteration had occurred. δ 13C and δ 15N values of collagen in modern bone are distinctly different for the two feeding types, and this distinction is preserved in most of the prehistoric samples. Our results suggest that postmortem alteration of dietary tracers in the inorganic phases of bone may be a problem at all archaeological sites and must be evaluated in each case. While collagen analyzed in this study was resistant to alteration, evaluation of the possibility of diagenetic alteration of its isotopic composition in bones from other

  4. Magnesium isotope compositions of Solar System materials determined by double spiking

    Science.gov (United States)

    Hin, R.; Lai, Y. J.; Coath, C.; Elliott, T.

    2015-12-01

    As a major element, magnesium is of interest for investigating large scale processes governing the formation and evolution of rocky planetary bodies. Determining the Mg isotope composition of the Earth and other planetary bodies has hence been a topic of interest ever since mass-dependent fractionation of 'non-traditional' stable isotopes has been used to study high-temperature processes. Published results, however, suffer from disagreement on the Mg isotope compositions of the Earth and chondrites [1-5], which is attributed to residual matrix effects. Nonetheless, most recent studied have converged towards a homogeneous (chondritic) Mg isotope composition in the Solar System [2-5]. However, in several of the recent studies there is a hint of a systematic difference of about 0.02-0.06‰ in the 26Mg/24Mg isotope compositions of chondrites and Earth. Such difference, however, is only resolvable by taking standard errors, which assumes robust data for homogenous sample sets. The discrepancies between various studies unfortunately undermine the confidence in such robustness and homogeneity. The issues with matrix effects during isotopic analyses can be overcome by using a double spike approach. Such methodology generally requires three isotope ratios to solve for three unknowns, a requirement that cannot be met for Mg. However, using a newly developed approach, we present Mg isotope compositions obtained by critical mixture double spiking. This new approach should allow greater confidence in the robustness of the data and hence enable improvement of. Preliminary data indicate that chondrites have a resolvable ~0.04‰ lighter 26Mg/24Mg than (ultra)mafic rocks from Earth, Mars and the eucrite parent body, which appear indistinguishable from each other. It seems implausible that this difference is caused by magmatic process such as partial melting or crystallisation. More likely, Mg isotopes are fractionated by a non-magmatic process during the formation of planets, e

  5. Hydrothermal impacts on trace element and isotope ocean biogeochemistry.

    Science.gov (United States)

    German, C R; Casciotti, K A; Dutay, J-C; Heimbürger, L E; Jenkins, W J; Measures, C I; Mills, R A; Obata, H; Schlitzer, R; Tagliabue, A; Turner, D R; Whitby, H

    2016-11-28

    Hydrothermal activity occurs in all ocean basins, releasing high concentrations of key trace elements and isotopes (TEIs) into the oceans. Importantly, the calculated rate of entrainment of the entire ocean volume through turbulently mixing buoyant hydrothermal plumes is so vigorous as to be comparable to that of deep-ocean thermohaline circulation. Consequently, biogeochemical processes active within deep-ocean hydrothermal plumes have long been known to have the potential to impact global-scale biogeochemical cycles. More recently, new results from GEOTRACES have revealed that plumes rich in dissolved Fe, an important micronutrient that is limiting to productivity in some areas, are widespread above mid-ocean ridges and extend out into the deep-ocean interior. While Fe is only one element among the full suite of TEIs of interest to GEOTRACES, these preliminary results are important because they illustrate how inputs from seafloor venting might impact the global biogeochemical budgets of many other TEIs. To determine the global impact of seafloor venting, however, requires two key questions to be addressed: (i) What processes are active close to vent sites that regulate the initial high-temperature hydrothermal fluxes for the full suite of TEIs that are dispersed through non-buoyant hydrothermal plumes? (ii) How do those processes vary, globally, in response to changing geologic settings at the seafloor and/or the geochemistry of the overlying ocean water? In this paper, we review key findings from recent work in this realm, highlight a series of key hypotheses arising from that research and propose a series of new GEOTRACES modelling, section and process studies that could be implemented, nationally and internationally, to address these issues.This article is part of the themed issue 'Biological and climatic impacts of ocean trace element chemistry'. © 2015 The Authors.

  6. Tracing anthropogenic thallium in soil using stable isotope compositions.

    Science.gov (United States)

    Kersten, Michael; Xiao, Tangfu; Kreissig, Katharina; Brett, Alex; Coles, Barry J; Rehkämper, Mark

    2014-08-19

    Thallium stable isotope data are used in this study, for the first time, to apportion Tl contamination in soils. In the late 1970s, a cement plant near Lengerich, Germany, emitted cement kiln dust (CKD) with high Tl contents, due to cocombustion of Tl-enriched pyrite roasting waste. Locally contaminated soil profiles were obtained down to 1 m depth and the samples are in accord with a binary mixing relationship in a diagram of Tl isotope compositions (expressed as ε(205)Tl, the deviation of the (205)Tl/(203)Tl ratio of a sample from the NIST SRM 997 Tl isotope standard in parts per 10(4)) versus 1/[Tl]. The inferred mixing endmembers are the geogenic background, as defined by isotopically light soils at depth (ε(205)Tl ≈ -4), and the Tl emissions, which produce Tl-enriched topsoils with ε(205)Tl as high as ±0. The latter interpretation is supported by analyses of the CKD, which is also characterized by ε(205)Tl ≈ ± 0, and the same ε(205)Tl value was found for a pyrite from the deposit that produced the cocombusted pyrite roasting waste. Additional measurements for samples from a locality in China, with outcrops of Tl sulfide mineralization and associated high natural Tl backgrounds, reveal significant isotope fractionation between soils (ε(205)Tl ≈ +0.4) and locally grown green cabbage (ε(205)Tl between -2.5 and -5.4). This demonstrates that biological isotope fractionation cannot explain the isotopically heavy Tl in the Lengerich topsoils and the latter are therefore clearly due to anthropogenic Tl emissions from cement processing. Our results thus establish that isotopic data can reinforce receptor modeling for the toxic trace metal Tl.

  7. Isotopic composition of steam samples from Lanzarote, Canary Islands

    Energy Technology Data Exchange (ETDEWEB)

    Arana, V. (CSIC, Madrid); Panichi, C.

    1974-12-01

    The isotopic analysis of the steam samples collected in the geothermal area of Lanzarote show that the values of delta D are practically constant, and those of delta /sup 18/O range in a shift of 17 /sup 0///sub 00/ reaching a maximum of +14.7 /sup 0///sub 00/ versus SMOW, this last value being the highest found in steam samples. This composition can be explained as a consequence of the isotopic exchange at high temperature between limestones and a mixture of marine and local meteoric waters. This interpretation agrees with previous geological and geophysical studies which consider that a promising geothermal field could exist in Lanzarote. (auth)

  8. Stable isotope mass spectrometry in petroleum exploration

    International Nuclear Information System (INIS)

    Mathur, Manju

    1997-01-01

    The stable isotope mass spectrometry plays an important role to evaluate the stable isotopic composition of hydrocarbons. The isotopic ratios of certain elements in petroleum samples reflect certain characteristics which are useful for petroleum exploration

  9. Elemental compositions of two extrasolar rocky planetesimals

    Energy Technology Data Exchange (ETDEWEB)

    Xu, S.; Jura, M.; Klein, B.; Zuckerman, B. [Department of Physics and Astronomy, University of California, Los Angeles, CA 90095-1562 (United States); Koester, D., E-mail: sxu@astro.ucla.edu, E-mail: jura@astro.ucla.edu, E-mail: kleinb@astro.ucla.edu, E-mail: ben@astro.ucla.edu, E-mail: koester@astrophysik.uni-kiel.de [Institut fur Theoretische Physik und Astrophysik, University of Kiel, D-24098 Kiel (Germany)

    2014-03-10

    We report Keck/HIRES and Hubble Space Telescope/COS spectroscopic studies of extrasolar rocky planetesimals accreted onto two hydrogen atmosphere white dwarfs, G29-38 and GD 133. In G29-38, eight elements are detected, including C, O, Mg, Si, Ca, Ti, Cr, and Fe while in GD 133, O, Si, Ca, and marginally Mg are seen. These two extrasolar planetesimals show a pattern of refractory enhancement and volatile depletion. For G29-38, the observed composition can be best interpreted as a blend of a chondritic object with some refractory-rich material, a result from post-nebular processing. Water is very depleted in the parent body accreted onto G29-38, based on the derived oxygen abundance. The inferred total mass accretion rate in GD 133 is the lowest of all known dusty white dwarfs, possibly due to non-steady state accretion. We continue to find that a variety of extrasolar planetesimals all resemble to zeroth order the elemental composition of bulk Earth.

  10. Dolomite clumped isotope constraints on the oxygen isotope composition of the Phanerozoic Sea

    Science.gov (United States)

    Ryb, U.; Eiler, J. M.

    2017-12-01

    The δ18O value of the Phanerozoic Sea has been debated several decades, largely motivated by an 8‰ increase in δ18O of sedimentary carbonates between the Cambrian and the present. Some previous studies have interpreted this increase to be a primary depositional signal, resulting from an increase in the 18O content of ocean water over time, or from a decrease in ocean temperature increasing the oxygen isotope fractionation between seawater and carbonates. In contrast, other studies have interpreted lower δ18O compositions as the products of diagenetic alteration at elevated burial temperatures. Here, we show that the Phanerozoic dolomite δ18O record overlaps with that of well-preserved calcite fossils, and use carbonate clumped isotope measurements of Cambrian to Pleistocene dolomites to calculate their formation temperatures and the isotopic compositions of their parent-waters. The observed variation in dolomite δ18O is largely explained by dolomite formation at burial temperatures of up to 158°C. The δ18O values of dolomite parent-waters range -2 to +12‰ and are correlated with formation temperatures. Such correlation is consistent with the modification of seawater (0±2‰, VSMOW) toward isotopically heavier compositions through water-rock reactions at elevated burial temperatures. The similarity between the dolomite and calcite δ18O records, and published clumped isotope-based calculations of water compositions, suggests that like dolomite, temporal variations of the calcite δ18O record may also be largely driven by diagenetic alteration. Finally, the relationship we observe between temperature of dolomitization and d18O of dolomite suggests platform carbonates generally undergo dolomitization through reaction with modified marine waters, and that there is no evidence those waters were ever significantly lower in d18O than the modern ocean.

  11. Geographic authentication of Asian rice (Oryza sativa L.) using multi-elemental and stable isotopic data combined with multivariate analysis.

    Science.gov (United States)

    Chung, Ill-Min; Kim, Jae-Kwang; Lee, Kyoung-Jin; Park, Sung-Kyu; Lee, Ji-Hee; Son, Na-Young; Jin, Yong-Ik; Kim, Seung-Hyun

    2018-02-01

    Rice (Oryza sativa L.) is the world's third largest food crop after wheat and corn. Geographic authentication of rice has recently emerged asan important issue for enhancing human health via food safety and quality assurance. Here, we aimed to discriminate rice of six Asian countries through geographic authentication using combinations of elemental/isotopic composition analysis and chemometric techniques. Principal components analysis could distinguish samples cultivated from most countries, except for those cultivated in the Philippines and Japan. Furthermore, orthogonal projection to latent structure-discriminant analysis provided clear discrimination between rice cultivated in Korea and other countries. The major common variables responsible for differentiation in these models were δ 34 S, Mn, and Mg. Our findings contribute to understanding the variations of elemental and isotopic compositions in rice depending on geographic origins, and offer valuable insight into the control of fraudulent labeling regarding the geographic origins of rice traded among Asian countries. Copyright © 2017 Elsevier Ltd. All rights reserved.

  12. High-precision measurements of seawater Pb isotope compositions by double spike thermal ionization mass spectrometry.

    Science.gov (United States)

    Paul, Maxence; Bridgestock, Luke; Rehkämper, Mark; van DeFlierdt, Tina; Weiss, Dominik

    2015-03-10

    A new method for the determination of seawater Pb isotope compositions and concentrations was developed, which combines and optimizes previously published protocols for the separation and isotopic analysis of this element. For isotopic analysis, the procedure involves initial separation of Pb from 1 to 2L of seawater by co-precipitation with Mg hydroxide and further purification by a two stage anion exchange procedure. The Pb isotope measurements are subsequently carried out by thermal ionization mass spectrometry using a (207)Pb-(204)Pb double spike for correction of instrumental mass fractionation. These methods are associated with a total procedural Pb blank of 28±21 pg (1sd) and typical Pb recoveries of 40-60%. The Pb concentrations are determined by isotope dilution (ID) on 50 mL of seawater, using a simplified version of above methods. Analyses of multiple aliquots of six seawater samples yield a reproducibility of about ±1 to ±10% (1sd) for Pb concentrations of between 7 and 50 pmol/kg, where precision was primarily limited by the uncertainty of the blank correction (12±4 pg; 1sd). For the Pb isotope analyses, typical reproducibilities (±2sd) of 700-1500 ppm and 1000-2000 ppm were achieved for (207)Pb/(206)Pb, (208)Pb/(206)Pb and (206)Pb/(204)Pb, (207)Pb/(204)Pb, (208)Pb/(204)Pb, respectively. These results are superior to literature data that were obtained using plasma source mass spectrometry and they are at least a factor of five more precise for ratios involving the minor (204)Pb isotope. Both Pb concentration and isotope data, furthermore, show good agreement with published results for two seawater intercomparison samples of the GEOTRACES program. Finally, the new methods were applied to a seawater depth profile from the eastern South Atlantic. Both Pb contents and isotope compositions display a smooth evolution with depth, and no obvious outliers. Compared to previous Pb isotope data for seawater, the (206)Pb/(204)Pb ratios are well correlated

  13. Modeling the carbon isotope composition of bivalve shells (Invited)

    Science.gov (United States)

    Romanek, C.

    2010-12-01

    The stable carbon isotope composition of bivalve shells is a valuable archive of paleobiological and paleoenvironmental information. Previous work has shown that the carbon isotope composition of the shell is related to the carbon isotope composition of dissolved inorganic carbon (DIC) in the ambient water in which a bivalve lives, as well as metabolic carbon derived from bivalve respiration. The contribution of metabolic carbon varies among organisms, but it is generally thought to be relatively low (e.g., 90%) in the shells from terrestrial organisms. Because metabolic carbon contains significantly more C-12 than DIC, negative excursions from the expected environmental (DIC) signal are interpreted to reflect an increased contribution of metabolic carbon in the shell. This observation contrasts sharply with modeled carbon isotope compositions for shell layers deposited from the inner extrapallial fluid (EPF). Previous studies have shown that growth lines within the inner shell layer of bivalves are produced during periods of anaerobiosis when acidic metabolic byproducts (e.g., succinic acid) are neutralized (or buffered) by shell dissolution. This requires the pH of EPF to decrease below ambient levels (~7.5) until a state of undersaturation is achieved that promotes shell dissolution. This condition may occur when aquatic bivalves are subjected to external stressors originating from ecological (predation) or environmental (exposure to atm; low dissolved oxygen; contaminant release) pressures; normal physiological processes will restore the pH of EPF when the pressure is removed. As a consequence of this process, a temporal window should also exist in EPF at relatively low pH where shell carbonate is deposited at a reduced saturation state and precipitation rate. For example, EPF chemistry should remain slightly supersaturated with respect to aragonite given a drop of one pH unit (6.5), but under closed conditions, equilibrium carbon isotope fractionation

  14. Deuterium isotope composition of palaeoinfiltration water trapped in speleothems

    International Nuclear Information System (INIS)

    Rozanski, K.

    1987-05-01

    Analytical and methodological aspects of combined isotope investigations of carbonate cave deposits are thoroughly discussed in the report. Weight is put on isotope analyses of fluid inclusions (D and 18 O content) extracted from speleothems of known age. Dating was done by the 230 Th/ 234 U ratio method. Isotopic analyses of speleothems originating from European caves allowed some important conclusions to be formulated regarding past climatic and environmental conditions prevailing over the European continent during the last 300,000 yrs: a) δD values of fluid inclusions suggest a remarkable constancy of the heavy-isotope content of European palaeoinfiltration waters recharged during interglacial periods, b) a climate-induced, long-term changes in isotopic composition of precipitation and surface air temperature over Europe can be characterized by the deuterium gradient of ca.1 4 deg./oo/deg. C, c) an apparent constancy of the continental gradient in deuterium content of European palaeoinfiltration waters as judged from the fluid inclusion data suggests that atmospheric circulation over Europe did not undergo substantial changes for at least 300,000 years

  15. Application of stable isotopes in ecological research : it's all elemental

    International Nuclear Information System (INIS)

    Rogers, K.M.

    2005-01-01

    Stable isotopes have been used traditionally in the physical sciences, primarily in geochemistry, sedimentology, and oceanography. Increasingly, however, stable isotopes are also being used in the biological sciences. Application of stable isotopes in ecological studies can provide new and innovative ways of examining a host of topics of fundamental importance to biologists. These topics include, among others, feeding ecology and food webs, nutrient flow and assimilation, habitat use, migration patterns, and distribution and discrimination of species subpopulations. Furthermore, ecological research with isotopes can be applied at many levels (i.e. tissue and organ, whole animal, population, community, and ecosystem). (author). 38 refs., 2 figs

  16. Measurements of the isotopic composition of galactic cosmic rays

    International Nuclear Information System (INIS)

    Herrstroem, N.Y.

    1985-01-01

    The galactic cosmic-ray boron and carbon isotopic composition has been measured. The boron measurement is the first ever made in nuclear emulsion. The carbon measurement has substantially improved the statistical assuracy in the determination of the 13 C abundance as compared to an earlier measurement using the same technique. Mass-spectra of cosmic-ray carbon and oxygen in different zenith angle intervals have been compared with calculated spectra. The method makes it possible to study experimentally the atmospheric influence on the primary cosmic-ray isotopic composition. Photometric measurements on fragments from oxygen-induced interactions in nuclear emulsion have been made. Accurate charge assignments have been made on all heavy fragments which has made it possible to study the interaction exclusively event-by-event. Measurements on the isotopic composition of primary cosmic-ray neom have been made. The data are from the Danish-French instrument on the HEAO-3 satellite. The rigidity dependent filtering of the cosmic rays by the Earth's magnetic field has been used. The energy dependence of the 22 Ne/ 20 Ne-ratio and its astrophysical implications are discussed. (Author)

  17. Measurements of flux and isotopic composition of soil carbon dioxide

    International Nuclear Information System (INIS)

    Gorczyca, Z.; Rozanski, K.; Kuc, T.

    2002-01-01

    The flux and isotope composition of soil CO 2 has been regularly measured at three sites located in the southern Poland, during the time period: January 1998 - October 2000. They represent typical ecosystems appearing in central Europe: (i) mixed forest; (ii) cultivated agricultural field; (iii) grassland. To monitor the flux and isotopic composition of soil CO 2 , a method based on the inverted cup principle was adopted. The flux of soil CO 2 reveals distinct seasonal fluctuations, with maximum values up to ca. 25 mmol/m 2 /h during sommer months and around ten times lower values during winter time. Also significant differences among the monitored sites were detected, the flux density of this gas being highest for the mixed forest site and ca. two times lower for the cultivated grassland. Carbon-13 content of the soil CO 2 reveals little seasonal variability, with δ 13 C values essentially reflecting the isotopic composition of the soil organic matter and the vegetation type. The carbon-14 content of soil CO 2 flux also reveals slight seasonality, with lower δ 14 C values recorded during winter time. Significantly lower δ 14 C values recorded during winter time. Significantly lower δ 14 C values were recorded at depth. (author)

  18. A 15N-poor isotopic composition for the solar system as shown by Genesis solar wind samples.

    Science.gov (United States)

    Marty, B; Chaussidon, M; Wiens, R C; Jurewicz, A J G; Burnett, D S

    2011-06-24

    The Genesis mission sampled solar wind ions to document the elemental and isotopic compositions of the Sun and, by inference, of the protosolar nebula. Nitrogen was a key target element because the extent and origin of its isotopic variations in solar system materials remain unknown. Isotopic analysis of a Genesis Solar Wind Concentrator target material shows that implanted solar wind nitrogen has a (15)N/(14)N ratio of 2.18 ± 0.02 × 10(-3) (that is, ≈40% poorer in (15)N relative to terrestrial atmosphere). The (15)N/(14)N ratio of the protosolar nebula was 2.27 ± 0.03 × 10(-3), which is the lowest (15)N/(14)N ratio known for solar system objects. This result demonstrates the extreme nitrogen isotopic heterogeneity of the nascent solar system and accounts for the (15)N-depleted components observed in solar system reservoirs.

  19. On the Effect of Planetary Stable Isotope Compositions on Growth and Survival of Terrestrial Organisms.

    Directory of Open Access Journals (Sweden)

    Xueshu Xie

    Full Text Available Isotopic compositions of reactants affect the rates of chemical and biochemical reactions. Usually it is assumed that heavy stable isotope enrichment leads to progressively slower reactions. Yet the effect of stable isotopes may be nonlinear, as exemplified by the "isotopic resonance" phenomenon. Since the isotopic compositions of other planets of Solar system, including Mars and Venus, are markedly different from terrestrial (e.g., deuterium content is ≈5 and ≈100 times higher, respectively, it is far from certain that terrestrial life will thrive in these isotopic conditions. Here we found that Martian deuterium content negatively affected survival of shrimp in semi-closed biosphere on a year-long time scale. Moreover, the bacterium Escherichia coli grows slower at Martian isotopic compositions and even slower at Venus's compositions. Thus, the biological impact of varying stable isotope compositions needs to be taken into account when planning interplanetary missions.

  20. Isotope-abundance variations and atomic weights of selected elements: 2016 (IUPAC Technical Report)

    Science.gov (United States)

    Coplen, Tyler B.; Shrestha, Yesha

    2016-01-01

    There are 63 chemical elements that have two or more isotopes that are used to determine their standard atomic weights. The isotopic abundances and atomic weights of these elements can vary in normal materials due to physical and chemical fractionation processes (not due to radioactive decay). These variations are well known for 12 elements (hydrogen, lithium, boron, carbon, nitrogen, oxygen, magnesium, silicon, sulfur, chlorine, bromine, and thallium), and the standard atomic weight of each of these elements is given by IUPAC as an interval with lower and upper bounds. Graphical plots of selected materials and compounds of each of these elements have been published previously. Herein and at the URL http://dx.doi.org/10.5066/F7GF0RN2, we provide isotopic abundances, isotope-delta values, and atomic weights for each of the upper and lower bounds of these materials and compounds.

  1. Study on the meat isotopic composition for origin identification

    Directory of Open Access Journals (Sweden)

    Irina Chernukha

    2018-03-01

    Full Text Available Russian consumer and governmental authorities are equally concerned to know where food products come from. This requires more accurate and specialized methods for the evaluation of geographical location. The following methods are used: chemometrics, histological and histochemical, genomic and proteomic, microbiological, immunochemical and mass spectrometric. Method of stable isotope analysis is becoming increasingly promising nowadays for the identification of meat and meat products' place of origin. The isotope ratios of the four elements - carbon, nitrogen, oxygen and hydrogen, are mainly determined. The method is successfully used to identify a country of origin of wines, juices and water. The aim of the research was to study the stable isotope ratios for pork and beef samples purchased in Moscow supermarkets (Russian Federation. The country of production of meat samples was determined according to specifications and/or labels. The geography of countries of meat samples origin includes Europe, both America continents and Australia. Databases collected by the All-Russian Scientific Research Institute of the Brewing, Non-Alcoholic and Wine Industrywere used for the analysis and interpretation of the results. Values of 13С/12С, δ13С, 18О/16О, δ18О, 2Н/1Н, δ2Н for 30 pork and beef samples from 13 countries were obtained. Differences in stable isotope ratios were found depending on place of origin. The data correlated with the oxygen isotope characteristics for wine, which were in the range from 2.5 to 4.5 ppm. According to the 13С/12С, δ13С results, the assumption was made about a false indication of the region for the beef sample. Despite the fact that beef was labeled as a product of Lithuania, the region of origin was most probably defined as Germany. The studies carried out showed the possibility to identify the region of raw meat origin by the stable isotope ratio.

  2. Isotopes and the Electron Configuration of the Blocks in the Periodic Table of Elements, upto the Last Element No.155

    Directory of Open Access Journals (Sweden)

    Khazan A.

    2011-04-01

    Full Text Available This is a theoretical study, which first manifests which connexion exists between isotopes and the electron blocks, and how the electron blocks are located in the version of the Periodic Table of Elements which ends with element No.155.

  3. Light Stable Isotopic Compositions of Enriched Mantle Sources: Resolving the Dehydration Paradox

    Science.gov (United States)

    Dixon, J. E.; Bindeman, I. N.; Kingsley, R. H.

    2017-12-01

    An outstanding puzzle in mantle geochemistry has been the origin and evolution of Earth's volatile components. The "dehydration paradox" refers to the following conundrum. Mantle compositions for some enriched mid-ocean ridge (MORB) and ocean island (OIB) basalts basalts require involvement of a mostly dehydrated slab component to explain the trace element ratios and radiogenic isotopic compositions, but a fully hydrated slab component to explain the stable isotopic compositions. Volatile and stable isotopic data on enriched MORB show a diversity of enriched components. Pacific PREMA-type basalts (H2O/Ce = 215 ± 30, δDSMOW = -45 ± 5 ‰) are similar to those in the north Atlantic (H2O/Ce = 220 ± 30; δDSMOW = -30 to -40 ‰). Basalts with EM-type signatures have regionally variable volatile compositions. North Atlantic EM-type basalts are wetter (H2O/Ce = 330 ± 30) and have isotopically heavier hydrogen (δDSMOW = -57 ± 5 ‰) than north Atlantic MORB. South Atlantic EM-type basalts are damp (H2O/Ce = 120 ± 10) with intermediate δDSMOW (-68 ± 2 ‰), similar to dDSMOW for Pacific MORB. North EPR EM-type basalts are dry (H2O/Ce = 110 ± 20) and isotopically light (δDSMOW = -94 ± 3 ‰). Boron and lithium isotopic ratios parallel the trends observed for dDSMOW. A multi-stage metasomatic and melting model accounts for the origin of the enriched components by extending the subduction factory concept down through the mantle transition zone, with slab temperature a key variable. The dehydration paradox is resolved by decoupling of volatiles from lithophile elements, reflecting primary dehydration of the slab followed by secondary rehydration and re-equilibration by fluids derived from subcrustal hydrous phases (e.g., antigorite) in cooler, deeper parts of the slab. The "expanded subduction factory" model includes melting at several key depths, including 1) 180 to 280 km, where EM-type mantle compositions are generated above slabs with average to hot thermal

  4. Depletion, cryptic metasomatism, and modal metasomatism of central European lithospheric mantle: evidence from elemental and Li isotope compositions of spinel peridotite xenoliths, Kozákov volcano, Czech Republic

    Czech Academy of Sciences Publication Activity Database

    Medaris Jr., L. G.; Ackerman, Lukáš; Jelínek, E.; Magna, T.

    2015-01-01

    Roč. 104, č. 8 (2015), s. 1925-1956 ISSN 1437-3254 Institutional support: RVO:67985831 Keywords : Central European lithospheric mantle * geochemistry * geothermometry * Li isotopes * spinel peridotite xenoliths Subject RIV: DD - Geochemistry Impact factor: 2.133, year: 2015

  5. Measurement of organic carbon stable isotope composition of different soil types by EA-IRMS system

    International Nuclear Information System (INIS)

    Qi Biao; Ding Lingling; Cui Jiehua; Wang Yanhong

    2009-01-01

    Element analyzer-isotope ratio mass spectrometers (EA-IRMS) is a rapid and precise method for measuring stable carbon isotope. Pure CO 2 reference gas was calibrated via international standard-Urea, and the δ 13 C us PDB value of pure CO 2 is (-29.523 ± 0.0181)%. Stability and linearity of the EA-IRMS system, precision of δ 13 C measurement for samples were tested through experimental comparison. Moreover, determination method of organic carbon stable isotope in soil was based on the system. The EA-IRMS system had well linearity when ion intensity ranged from 1.0 to 7.0V, and it excelled the total linearity when the ion intensity was from 1.5 to 5.0V, and the accurate result of δ 13 C for sample analysis could be obtained with precision of 0.015%. If carbon content in sample is more than 5μg, the requirement for analyzing accurate result of δ 13 C could be achieved. The organic carbon stable isotope was measured in 18 different types soil samples, the average natural abundance of 13 C was 1.082%, and the organic carbon stable isotope composition was significantly different among different type soils. (authors)

  6. A Procedure to Determine the Coordinated Chromium and Calcium Isotopic Composition of Astromaterials Including the Chelyabinsk Meteorite

    Science.gov (United States)

    Tappa, M. J.; Mills, R. D.; Ware, B.; Simon, J. I.

    2014-01-01

    The isotopic compositions of elements are often used to characterize nucelosynthetic contributions in early Solar System objects. Coordinated multiple middle-mass elements with differing volatilities may provide information regarding the location of condensation of early Solar System solids. Here we detail new procedures that we have developed to make high-precision multi-isotope measurements of chromium and calcium using thermal ionization mass spectrometry, and characterize a suite of chondritic and terrestrial material including two fragments of the Chelyabinsk LL-chondrite.

  7. Trace elements and isotope data of the Um Garayat gold deposit, Wadi Allaqi district, Egypt

    Science.gov (United States)

    Zoheir, Basem; Emam, Ashraf; Pitcairn, Iain K.; Boskabadi, Arman; Lehaye, Yann; Cooper, Matthew J.

    2018-04-01

    Trace element composition of sulfides and O, C, Sr and S isotopic data are assessed to constrain the evolution and potential fluid and metal sources of the Um Garayat gold deposit. Ore microscopy and BSE investigations of quartz veins show blocky arsenopyrite and pyrite replaced in part by pyrrhotite, chalcopyrite, sphalerite, galena, and gersdorffite. Free-milling gold occurs commonly in close association with the late sulfides, and along fractures in pyrite. On the other hand, recrystallized pyrite is disseminated in host metavolcaniclastic/metasedimentary rocks that commonly contain carbonaceous material. In situ LA-ICP-MS analysis of sulfides shows the recrystallized pyrite enriched in most trace elements, while blocky pyrite contains only some traces of arsenic. Detected concentrations of gold (up to 17 ppm) were only reported in arsenopyrite disseminated in quartz veins. The δ34S values of blocky pyrite and pyrrhotite in quartz veins define a narrow range (1.6 to 3.7‰), suggesting a homogenous sulfur source which is consistent with the dominantly mafic host rocks. The recrystallized pyrite has a distinctive sulfur isotope composition (δ34S - 9.3 to - 10.6‰), which is rather comparable to diagenetic sulfides. Hydrothermal carbonate in quartz veins and wallrock have nearly constant values of δ18O (10.5 to 11.9‰) and δ13C (- 4.2 to - 5.5‰). Based on constraints from mineral assemblages and chlorite thermometry, data of six samples indicate that carbonate precipitation occurred at 280 °C from a homogenous hydrothermal fluid with δ18OH2O 4.4 ± 0.7‰ and δ13C = 3.7 ± 0.8‰. Strontium isotope values of two samples (87Sr/86Sr = 0.7024 and 0.7025) are similar to the initial 87Sr/86Sr ratios of island arc metabasalts ( 710 Ma) in the South Eastern Desert. The generally homogenous sulfur, C, O, Sr isotope data are suggestive of metamorphogenic fluids, likely produced from dominantly mafic volcanic rocks at the greenschist-amphibolite facies transition.

  8. Raman spectral, elemental, crystallinity, and oxygen-isotope variations in conodont apatite during diagenesis

    Science.gov (United States)

    Zhang, Lei; Cao, Ling; Zhao, Laishi; Algeo, Thomas J.; Chen, Zhong-Qiang; Li, Zhihong; Lv, Zhengyi; Wang, Xiangdong

    2017-08-01

    Conodont apatite has long been used in paleoenvironmental studies, often with minimal evaluation of the influence of diagenesis on measured elemental and isotopic signals. In this study, we evaluate diagenetic influences on conodonts using an integrated set of analytical techniques. A total of 92 points in 19 coniform conodonts from Ordovician marine units of South China were analyzed by micro-laser Raman spectroscopy (M-LRS), laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), high-resolution X-ray microdiffraction (HXRD), and secondary ion mass spectrometry (SIMS). Each conodont element was analyzed along its full length, including the albid crown, hyaline crown, and basal body, in either a whole specimen (i.e., reflecting the composition of its outer layer) or a split specimen (i.e., reflecting the composition of its interior). In the conodonts of this study, the outer surfaces consist of hydroxyfluorapatite and the interiors of strontian hydroxyfluorapatite. Ionic substitutions resulted in characteristic Raman spectral shifts in the position (SS1) and width (SS2) of the ν1-PO43- stretching band. Although multiple elements were enriched (Sr2+, Mg2+) and depleted (Fe3+, Mn2+, Ca2+) during diagenesis, geochemical modeling constraints and known Raman spectral patterns suggest that Sr uptake was the dominant influence on diagenetic redshifts of SS1. All study specimens show lower SS2 values than modern bioapatite and synthetic apatite, suggesting that band width decreases with time in ancient bioapatite, possibly through an annealing process that produces larger, more uniform crystal domains. Most specimens consist mainly of amorphous or poorly crystalline apatite, which is inferred to represent the original microstructure of conodonts. In a subset of specimens, some tissues (especially albid crown) exhibit an increased degree of crystallinity developed through aggrading neomorphism. However, no systematic relationship was observed between

  9. Stable isotopes

    International Nuclear Information System (INIS)

    Brazier, J.L.; Guinamant, J.L.

    1995-01-01

    According to the progress which has been realised in the technology of separating and measuring isotopes, the stable isotopes are used as preferable 'labelling elements' for big number of applications. The isotopic composition of natural products shows significant variations as a result of different reasons like the climate, the seasons, or their geographic origins. So, it was proved that the same product has a different isotopic composition of alimentary and agriculture products. It is also important in detecting the pharmacological and medical chemicals. This review article deals with the technology, like chromatography and spectrophotometry, adapted to this aim, and some important applications. 17 refs. 6 figs

  10. The hydrogen isotopic composition of kaolin minerals in Japan

    International Nuclear Information System (INIS)

    Marumo, Katsumi; Nagasawa, Keinosuke; Kuroda, Yoshimasu.

    1979-01-01

    Hydrogen isotopic composition (D/H ratio) was determined for kaolin minerals from geothermal areas and sedimentary and hydrothermal kaolin deposits in Japan. On the Ohnuma, Matsukawa, and Ohtake geothermal areas, the hydrogen isotopic fractionation factor between kaolin minerals and water was calculated to fall between 0.97 and 0.99 for the temperature range of 50 to 200 0 C, a fact which shows that the temperature of formation has no important effect on the D/H ratio of kaolin minerals. D/H ratio of kaolinites and dickites from many kaolin deposits shows local variation, and seems to correlate with isotopic variation of the present-day meteoric surface water. Exceptions are seen in some kaolin deposits such as Shokozan, Hiroshima Prefecture, where kaolinite and dickite have considerably high values of D/H ratio, and seem to have reacted with water rich in deuterium. D/H ratio of halloysite is not correlated with that of the present-day meteoric surface water. As Lawrence and Taylor (1971) pointed out, the original D/H ratio of constitutional water of halloysite is not preserved because of the isotopic exchange between the interlayer water and the constitutional water. (author)

  11. Clumped-isotope geochemistry of carbonates: A new tool for the reconstruction of temperature and oxygen isotope composition of seawater

    Energy Technology Data Exchange (ETDEWEB)

    Bernasconi, Stefano M., E-mail: Stefano.bernasconi@erdw.ethz.ch [Geological Institute, ETH Zuerich, Sonneggstrasse 5, 8092 Zuerich (Switzerland); Schmid, Thomas W.; Grauel, Anna-Lena [Geological Institute, ETH Zuerich, Sonneggstrasse 5, 8092 Zuerich (Switzerland); Mutterlose, Joerg [Institut fuer Geologie, Mineralogie und Geophysik, Ruhr Universitaet Bochum, Universitaetsstr. 150, 44801 Bochum (Germany)

    2011-06-15

    Highlights: > Clumped-isotope thermometry of carbonates is discussed. > Clumped isotopes of Belemnites show higher sea surface temperatures than commonly assumed for the lower Cretaceous. > The potential of clumped-isotope measurement on foraminifera is discussed. - Abstract: Clumped-isotope geochemistry deals with State of ordering of rare isotopes in molecules, in particular with their tendency to form bonds with other rare isotopes rather than with the most abundant ones. Among its possible applications, carbonate clumped-isotope thermometry is the one that has gained most attention because of the wide potential of applications in many disciplines of the earth sciences. In particular, it allows reconstructing the temperature of formation of carbonate minerals without knowledge of the isotopic composition of the water from which they were formed. In addition, the O isotope composition of the waters from which they were formed can be calculated using the {delta}{sup 18}O of the same carbonate sample. This feature offers new approaches in paleoclimatology for reconstructing past global geochemical cycles. In this contribution two applications of this method are presented. First the potential of a new analytical method of measurement of clumped isotopes on small samples of foraminifera, for high-resolution SST and seawater {delta}{sup 18}O reconstructions from marine sediments is shown. Furthermore the potential of clumped isotope analysis of belemnites, for reconstructing seawater {delta}{sup 18}O and temperatures in the Cretaceous is shown.

  12. On-line hydrogen-isotope measurements of organic samples using elemental chromium: An extension for high temperature elemental-analyzer techniques

    Science.gov (United States)

    Gehre, Matthias; Renpenning, Julian; Gilevska, Tetyana; Qi, Haiping; Coplen, Tyler B.; Meijer, Harro A.J.; Brand, Willi A.; Schimmelmann, Arndt

    2015-01-01

    The high temperature conversion (HTC) technique using an elemental analyzer with a glassy carbon tube and filling (temperature conversion/elemental analysis, TC/EA) is a widely used method for hydrogen isotopic analysis of water and many solid and liquid organic samples with analysis by isotope-ratio mass spectrometry (IRMS). However, the TC/EA IRMS method may produce inaccurate δ2H results, with values deviating by more than 20 mUr (milliurey = 0.001 = 1‰) from the true value for some materials. We show that a single-oven, chromium-filled elemental analyzer coupled to an IRMS substantially improves the measurement quality and reliability for hydrogen isotopic compositions of organic substances (Cr-EA method). Hot chromium maximizes the yield of molecular hydrogen in a helium carrier gas by irreversibly and quantitatively scavenging all reactive elements except hydrogen. In contrast, under TC/EA conditions, heteroelements like nitrogen or chlorine (and other halogens) can form hydrogen cyanide (HCN) or hydrogen chloride (HCl) and this can cause isotopic fractionation. The Cr-EA technique thus expands the analytical possibilities for on-line hydrogen-isotope measurements of organic samples significantly. This method yielded reproducibility values (1-sigma) for δ2H measurements on water and caffeine samples of better than 1.0 and 0.5 mUr, respectively. To overcome handling problems with water as the principal calibration anchor for hydrogen isotopic measurements, we have employed an effective and simple strategy using reference waters or other liquids sealed in silver-tube segments. These crimped silver tubes can be employed in both the Cr-EA and TC/EA techniques. They simplify considerably the normalization of hydrogen-isotope measurement data to the VSMOW-SLAP (Vienna Standard Mean Ocean Water-Standard Light Antarctic Precipitation) scale, and their use improves accuracy of the data by eliminating evaporative loss and associated isotopic fractionation while

  13. On-line hydrogen-isotope measurements of organic samples using elemental chromium: an extension for high temperature elemental-analyzer techniques.

    Science.gov (United States)

    Gehre, Matthias; Renpenning, Julian; Gilevska, Tetyana; Qi, Haiping; Coplen, Tyler B; Meijer, Harro A J; Brand, Willi A; Schimmelmann, Arndt

    2015-01-01

    The high temperature conversion (HTC) technique using an elemental analyzer with a glassy carbon tube and filling (temperature conversion/elemental analysis, TC/EA) is a widely used method for hydrogen isotopic analysis of water and many solid and liquid organic samples with analysis by isotope-ratio mass spectrometry (IRMS). However, the TC/EA IRMS method may produce inaccurate δ(2)H results, with values deviating by more than 20 mUr (milliurey = 0.001 = 1‰) from the true value for some materials. We show that a single-oven, chromium-filled elemental analyzer coupled to an IRMS substantially improves the measurement quality and reliability for hydrogen isotopic compositions of organic substances (Cr-EA method). Hot chromium maximizes the yield of molecular hydrogen in a helium carrier gas by irreversibly and quantitatively scavenging all reactive elements except hydrogen. In contrast, under TC/EA conditions, heteroelements like nitrogen or chlorine (and other halogens) can form hydrogen cyanide (HCN) or hydrogen chloride (HCl) and this can cause isotopic fractionation. The Cr-EA technique thus expands the analytical possibilities for on-line hydrogen-isotope measurements of organic samples significantly. This method yielded reproducibility values (1-sigma) for δ(2)H measurements on water and caffeine samples of better than 1.0 and 0.5 mUr, respectively. To overcome handling problems with water as the principal calibration anchor for hydrogen isotopic measurements, we have employed an effective and simple strategy using reference waters or other liquids sealed in silver-tube segments. These crimped silver tubes can be employed in both the Cr-EA and TC/EA techniques. They simplify considerably the normalization of hydrogen-isotope measurement data to the VSMOW-SLAP (Vienna Standard Mean Ocean Water-Standard Light Antarctic Precipitation) scale, and their use improves accuracy of the data by eliminating evaporative loss and associated isotopic fractionation while

  14. Radio-isotopic apparatus for analyzing low atomic number elements by fluorescence

    International Nuclear Information System (INIS)

    Robert, Andre; Martinelli, Pierre; Daniel, Georges; Laflotte, Jean-Luc

    1969-10-01

    An apparatus is described for analyzing light elements of atomic number between 6 and 24 by X-fluorescence. The samples are excited by means of X or α isotopic sources. Various examples of analytical determinations are given. (author) [fr

  15. Measurement of plutonium isotopic composition by gamma-ray spectroscopy

    International Nuclear Information System (INIS)

    Kim, J. S.; Shin, J. S.; Ahn, J. S.

    1998-01-01

    The technology of the analysis of plutonium isotopic ratio is independent of the measurement geometry and applicable to samples of physical and chemical composition. Three standard plutonium samples were measured in the HPGe system. The results showed that CRM 136 and CRM 137 containing 238 Pu(0.223%) and 238 Pu(0.268%) were 18.4% and 14.2% error and CRM 138 of 238 Pu(0.01%) was 76% error. However the analysis represented less than 1.6% and 9% error in the three standard samples of highly involved 239 Pu and 240 Pu. Therefore, gamma-ray spectroscopy is very effective in the plutonium isotope analysis, having greater than 10% in content

  16. Geochemistry of CI chondrites: Major and trace elements, and Cu and Zn Isotopes

    Science.gov (United States)

    Barrat, J. A.; Zanda, B.; Moynier, F.; Bollinger, C.; Liorzou, C.; Bayon, G.

    2012-04-01

    In order to check the heterogeneity of the CI chondrites and determine the average composition of this group of meteorites, we analyzed a series of six large chips (weighing between 0.6 and 1.2 g) of Orgueil prepared from five different stones. In addition, one sample from each of Ivuna and Alais was analyzed. Although the sizes of the chips used in this study were “large”, our results show evidence for minor chemical heterogeneity in Orgueil, particularly for alkali elements and U. After removal of one outlier sample, the spread of the results is considerably reduced. For most of the 46 elements analyzed in this study, the average composition calculated for Orgueil is in very good agreement with previous CI estimates. This average, obtained with a “large” mass of samples, is analytically homogeneous and is suitable for normalization purposes. Finally, the Cu and Zn isotopic ratios are homogeneously distributed within the CI parent body with a spread of less than 100 ppm per atomic mass unit (amu).

  17. Origin of the Moon Unveiled by its Heavy Iron Isotope Composition

    Science.gov (United States)

    Poitrasson, F.; Halliday, A. N.; Lee, D.; Levasseur, S.; Teutsch, N.

    2002-12-01

    The origin of the Moon has long been of interest and although the Giant Impact theory is currently the preferred explanation, unequivocal supporting evidence has been lacking. We have measured the iron isotope compositions of Shergotty-Nakhla-Chassigny meteorites and eucrites thought to come from Mars and Vesta, as well as samples from the Moon and the mafic Earth using high precision plasma source mass spectrometry. The mean iron isotope composition of the lunar samples, expressed in the conventional delta notation (d57Fe/54Fe) with respect to the IRMM-14 isotopic standard, is heavier (0.221 per mil (0.041: one standard deviation, 10 samples)) than those of the Earth (0.119 per mil (0.044, 7 samples)), which themselves are heavier than Martian meteorites (0.009 per mil (0.024, 6 samples)) and the eucrites measured (0.033 per mil (0.038, 7 samples)). Student's t-test calculations show that the Moon and Earth means are different from each other and from those of the other planetary bodies at >99% level of significance. The iron isotope compositions show no simple relationship with planetary heliocentric position, mantle oxygen fugacity, volatile content, or planet size. Similarly, these results do not support an origin of the Moon through co-accretion with the Earth, or as a fragment ejected from the Earth's mantle, or as another planet captured by the early Earth. In contrast, these data can be explained if the Earth, and especially the Moon, went through partial vaporisation and condensation leading to kinetic iron isotopic fractionation. Our data are also consistent with the suggested levels of enrichment of refractory elements for the bulk Earth and Moon. These new iron isotope results thus provide strong support for the origin of the Moon through a giant impact between the proto-Earth and another planet. Raleigh kinetic fractionation calculations indicate that only 1% loss of the current Fe budget of the Moon is required to explain its heavier isotopic

  18. A revision in hydrogen isotopic composition of USGS42 and USGS43 human-hair stable isotopic reference materials for forensic science

    Science.gov (United States)

    Coplen, Tyler B.; Qi, Haiping

    2016-01-01

    The hydrogen isotopic composition (δ2HVSMOW-SLAP) of USGS42 and USGS43 human hair stable isotopic reference materials, normalized to the VSMOW (Vienna-Standard Mean Ocean Water)–SLAP (Standard Light Antarctic Precipitation) scale, was originally determined with a high temperature conversion technique using an elemental analyzer (TC/EA) with a glassy carbon tube and glassy carbon filling and analysis by isotope-ratio mass spectrometer (IRMS). However, the TC/EA IRMS method can produce inaccurate δ2HVSMOW-SLAPresults when analyzing nitrogen-bearing organic substances owing to the formation of hydrogen cyanide (HCN), leading to non-quantitative conversion of a sample into molecular hydrogen (H2) for IRMS analysis. A single-oven, chromium-filled, elemental analyzer (Cr-EA) coupled to an IRMS substantially improves the measurement quality and reliability of hydrogen isotopic analysis of hydrogen- and nitrogen-bearing organic material because hot chromium scavenges all reactive elements except hydrogen. USGS42 and USGS43 human hair isotopic reference materials have been analyzed with the Cr-EA IRMS method, and the δ2HVSMOW-SLAP values of their non-exchangeable hydrogen fractions have been revised:where mUr = 0.001 = ‰. On average, these revised δ2HVSMOW-SLAP values are 5.7 mUr more positive than those previously measured. It is critical that readers pay attention to the δ2HVSMOW-SLAP of isotopic reference materials in publications as they may need to adjust the δ2HVSMOW–SLAP measurement results of human hair in previous publications to ensure all results are on the same isotope-delta scale.

  19. New neutron-deficient isotopes of barium and rare-earth elements

    CERN Document Server

    Bogdanov, D D; Karnaukhov, V A; Petrov, L A; Plochocki, A; Subbotin, V G; Voboril, J

    1976-01-01

    The authors present an investigation of the short-lived neutron- deficient isotopes of barium and rare-earth elements. By using the BEMS-2 isotope separator on a heavy ion beam, 19 new isotopes were produced with mass numbers ranging from 117 to 138. Five of these (/sup 117/Ba, /sup 129,131/Nd and /sup 133,135/Sm) turned out to be delayed proton emitters. The beta -decay probabilities for the new isotopes have been analyzed in terms of the beta -strength function. An analysis of the proton spectrum shape has been performed using the statistical model for delayed proton emission.

  20. Strontium isotopic and trace element geochemistry of the saddle mountains and Grande Ronde Basalts of the Columbia River Basalt Group

    International Nuclear Information System (INIS)

    Nelson, D.O.

    1980-01-01

    The Columbia River Basalt (CRB) group displays significant variations in major and trace element and Sr isotopic compositions. These compositions reflect complex and variable origins for the CRB magmas. Among the most varied is the Saddle Mountains Basalt (SMB) in which Sr ratios vary from 0.7078 to 0.7147 +- 0.002. The higher ratios reflect contamination through consistent correlations with major element compositions. Modeling suggests contamination by assimilation of 4.4 to 9.4 wt % of radiogenic crustal rocks. High delta 18 O values (up to +7.68 per mil) support the model. Age and field relations suggest that the contamination flowrocks are not the result of progressive contamination of a single magma, but rather reflect the contamination of independent magmas during this ascent

  1. Osmium Isotope Compositions of Komatiite Sources Through Time

    Science.gov (United States)

    Walker, R. J.

    2001-12-01

    Extending Os isotopic measurements to ancient plume sources may help to constrain how and when the well-documented isotopic heterogeneities in modern systems were created. Komatiites and picrites associated with plume-related volcanism are valuable tracers of the Os isotopic composition of plumes because of their typically high Os concentrations and relatively low Re/Os. Re-Os data are now available for a variety of Phanerozoic, Proterozoic and Archean komatiites and picrites. As with modern plumes, the sources of Archean and Proterozoic komatiites exhibit a large range of initial 187Os/188Os ratios. Most komatiites are dominated by sources with chondritic Os isotopic compositions (e.g. Song La; Norseman-Wiluna; Pyke Hill; Alexo), though some (e.g. Gorgona) derive from heterogeneous sources. Of note, however, two ca. 2.7 Ga systems, Kostomuksha (Russia) and Belingwe (Zimbabwe), have initial ratios enriched by 2-3% relative to the contemporary convecting upper mantle. These results suggest that if the 187Os enrichment was due to the incorporation of minor amounts of recycled crust into the mantle source of the rocks, the crust formed very early in Earth history. Thus, the Os results could reflect derivation of melt from hybrid mantle whose composition was modified by the addition of mafic crustal material that would most likely have formed between 4.2 and 4.5 Ga. Alternately, the mantle sources of these komatiites may have derived a portion of their Os from the putative 187Os - and 186Os -enriched outer core. For this hypothesis to be applicable to Archean rocks, an inner core of sufficient mass would have to have crystallized sufficiently early in Earth history to generate an outer core with 187Os enriched by at least 3% relative to the chondritic average. Using the Pt-Re-Os partition coefficients espoused by our earlier work, and assuming linear growth of the inner core started at 4.5 Ga and continued to present, would yield an outer core at 2.7 Ga with a gamma Os

  2. Ocean circulation and shelf processes in the Arctic, Mediterranean traced by radiogenic neodymium isotopes, rare earth elements and stable oxygen isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Laukert, Georgi

    2017-02-20

    Disentangling the sources, distribution and mixing of water masses involved in the transport and transfer of heat and freshwater in the Arctic Mediterranean (i.e. the Arctic Ocean and the Nordic Seas, AM) is critical for the understanding of present and future hydrological changes in the high-latitude regions. This study refines the knowledge of water mass circulation in the AM and provides new insights into the processes occurring on the Arctic shelves and in high-latitude estuaries. A multi-proxy approach is used combining dissolved radiogenic Nd isotopes (ε{sub Nd}), rare earth elements (REEs) and stable oxygen isotopes (δ{sup 18}O) together with standard hydrographic tracers. The sources, distribution and mixing of water masses that circulate in the AM and pass the Fram Strait are assessed through evaluation of dissolved ε{sub Nd} and REE, and δ{sup 18}O data obtained from samples recovered in 2012, 2014 and 2015, and through a compilation and reassessment of literature Nd isotope and concentration data previously reported for other sites within the AM. The Nd isotope and REE distribution in the central Fram Strait and the open AM is shown to primarily reflect the lateral advection of water masses and their mixing, whereas seawater-particle interactions exert important control only above the shelf regions. New insights into the processes occurring in high latitude estuaries are provided by dissolved Nd isotope and REE compositions together with δ{sup 18}O data for the Laptev Sea based on filtered samples recovered in 2012, 2013 and 2014. A combination of REE removal through coagulation of nanoparticles and colloids and REE redistribution within the water column through formation and melting of sea ice and river ice is suggested to account for the distribution of all REEs, while no REE release from particles is observed. The ice-related processes contribute to the redistribution of other elements and ultimately may also affect primary productivity in high

  3. Stable isotope composition of atmospheric carbon monoxide. A modelling study

    International Nuclear Information System (INIS)

    Gromov, Sergey S.

    2014-01-01

    This study aims at an improved understanding of the stable carbon and oxygen isotope composition of the carbon monoxide (CO) in the global atmosphere by means of numerical simulations. At first, a new kinetic chemistry tagging technique for the most complete parameterisation of isotope effects has been introduced into the Modular Earth Submodel System (MESSy) framework. Incorporated into the ECHAM/MESSy Atmospheric Chemistry (EMAC) general circulation model, an explicit treatment of the isotope effects on the global scale is now possible. The expanded model system has been applied to simulate the chemical system containing up to five isotopologues of all carbon- and oxygen-bearing species, which ultimately determine the δ 13 C, δ 18 O and Δ 17 O isotopic signatures of atmospheric CO. As model input, a new stable isotope-inclusive emission inventory for the relevant trace gases has been compiled. The uncertainties of the emission estimates and of the resulting simulated mixing and isotope ratios have been analysed. The simulated CO mixing and stable isotope ratios have been compared to in-situ measurements from ground-based observatories and from the civil-aircraft-mounted CARIBIC-1 measurement platform. The systematically underestimated 13 CO/ 12 CO ratios of earlier, simplified modelling studies can now be partly explained. The EMAC simulations do not support the inferences of those studies, which suggest for CO a reduced input of the highly depleted in 13 C methane oxidation source. In particular, a high average yield of 0.94 CO per reacted methane (CH 4 ) molecule is simulated in the troposphere, to a large extent due to the competition between the deposition and convective transport processes affecting the CH 4 to CO reaction chain intermediates. None of the other factors, assumed or disregarded in previous studies, however hypothesised to have the potential in enriching tropospheric CO in 13 C, were found significant when explicitly simulated. The

  4. Laser ionization time of flight mass spectrometer for isotope mass detection and elemental analysis of materials

    Science.gov (United States)

    Ahmed, Nasar; Ahmed, Rizwan; Umar, Z. A.; Aslam Baig, M.

    2017-08-01

    In this paper we present the construction and modification of a linear time-of-flight mass spectrometer to improve its mass resolution. This system consists of a laser ablation/ionization section based on a Q-switched Nd:YAG laser (532 nm, 500 mJ, 5 ns pulse duration) integrated with a one meter linear time-of-flight mass spectrometer coupled with an electric sector and a magnetic lens and outfitted with a channeltron electron multiplier for ion detection. The resolution of the system has been improved by optimizing the accelerating potential and inserting a magnetic lens after the extraction region. The isotopes of lithium, lead and cadmium samples have been resolved and detected in accordance with their natural abundance. The capability of the system has been further exploited to determine the elemental composition of a brass alloy, having a certified composition of zinc and copper. Our results are in excellent agreement with its certified composition. This setup is found to be extremely efficient and convenient for fast analyses of any solid sample.

  5. Extreme Hf-Os Isotope Compositions in Hawaiian Peridotite Xenoliths: Evidence for an Ancient Recycled Lithosphere

    Science.gov (United States)

    Bizimis, M.; Lassiter, J. C.; Salters, V. J.; Sen, G.; Griselin, M.

    2004-12-01

    We report on the first combined Hf-Os isotope systematics of spinel peridotite xenoliths from the Salt Lake Crater (SLC), Pali and Kaau (PK) vents from the island of Oahu, Hawaii. These peridotites are thought to represent the Pacific oceanic lithosphere beneath Oahu, as residues of MORB-type melting at a paleo-ridge some 80-100Ma ago. Clinopyroxene mineral separates in these peridotites have very similar Nd and Sr isotope compositions with the post erosional Honolulu Volcanics (HV) lavas that bring these xenoliths to the surface. This and their relatively elevated Na and LREE contents suggest that these peridotites are not simple residues of MORB-type melting but have experience some metasomatic enrichment by the host HV lavas. However, the SLC and PK xenoliths show an extreme range in Hf isotope compositions towards highly radiogenic values (ɛ Hf= 7-80), at nearly constant Nd isotope compositions (ɛ Nd= 7-10), unlike any OIB or MORB basalt. Furthermore, these Oahu peridotites show a bimodal distribution in their bulk rock 187Os/186Os ratios: the PK peridotites have similar ratios to the abyssal peridotites (0.130-0.1238), while the SLC peridotites have highly subchondritic ratios (0.1237-0.1134) that yield 500Ma to 2Ga Re-depletion ages. Hf-Os isotopes show a broad negative correlation whereby the samples with the most radiogenic 176Hf/177Hf have the most unradiogenic 187Os/186Os ratios. Based on their combined Hf-Os-Nd isotope and major element compositions, the PK peridotites can be interpreted as fragments of the Hawaiian lithosphere, residue of MORB melting 80-100Ma ago, that have been variably metasomatized by the host HV lavas. In contrast, the extreme Hf-Os isotope compositions of the SLC peridotites suggest that they cannot be the source nor residue of any kind of Hawaiian lavas, and that Hf and Os isotopes survived the metasomatism or melt-rock reaction that has overprinted the Nd and Sr isotope compositions of these peridotites. The ancient (>1Ga

  6. Source rock identification of sediments using trace element ratios and 13C isotope data - a case study from Pondicherry region

    International Nuclear Information System (INIS)

    Tirumalesh, K.; Kulkarni, U.P.; Singh, Gursharan; Ramakumar, K.L.; Chidambaram, S.

    2012-01-01

    Compositional characteristics of source rocks are generally well recorded in sedimentary deposits and provide valuable information about nature of source rocks even though weathering, physical sorting and deposition environment influence the sediment geochemistry. In this paper we report major, trace element and 13 C isotope data of cutting samples collected from Quaternary, Tertiary and Cretaceous formations in Pondicherry area. The distribution patterns and inter elemental correlations are used to identify source rock composition and carbon isotope compositions to understand the sediment deposition conditions. Mineralogy of the bulk sediment indicates presence of Quartz, K-feldspar, Calcite, Mg-calcite, Aragonite and Clay minerals. Compared to upper continental crust values most of these sediments show lower concentration of all elements except Ca and Zn at some depths. The depletion is probably associated with weathering of feldspar and removal of elements through solution. This also increases the proportion of quartz relative to source rock. The ratios of redox sensitive elements (Th/U) infer oxic weathering in shallow sediments. Elemental ratios (La/Sc, Th/Sc, Th/Cr, Th/Co) and ternary plots (La-Th-Sc and Th-Hf-Co) indicate contribution of felsic source rocks with varying degree of weathering. These plots also infer the inherent heterogeneity in the source rocks. Hafnium correlations with other trace elements suggest contribution of Tonalitic rocks in addition to granite to these sediments. The geochemical characteristics of the sediments are found to be similar to that of sediments belonging to similar geology in nearby regions. Presence of shallow marine condition during the sedimentation is inferred from the detrital index (DI) values, which is further supported by the presence of fibrous clay minerals in ESEM scans. This study also brings out the utility of δ 13 C information to reinforce the geochemical and mineralogical inferences. (author)

  7. Magma mixing and the generation of isotopically juvenile silicic magma at Yellowstone caldera inferred from coupling 238U–230Th ages with trace elements and Hf and O isotopes in zircon and Pb isotopes in sanidine

    Science.gov (United States)

    Stelten, Mark E.; Cooper, Kari M.; Vazquez, Jorge A.; Reid, Mary R.; Barfod, Gry H.; Wimpenny, Josh; Yin, Qing-Zhu

    2013-01-01

    The nature of compositional heterogeneity within large silicic magma bodies has important implications for how silicic reservoirs are assembled and evolve through time. We examine compositional heterogeneity in the youngest (~170 to 70 ka) post-caldera volcanism at Yellowstone caldera, the Central Plateau Member (CPM) rhyolites, as a case study. We compare 238U–230Th age, trace-element, and Hf isotopic data from zircons, and major-element, Ba, and Pb isotopic data from sanidines hosted in two CPM rhyolites (Hayden Valley and Solfatara Plateau flows) and one extracaldera rhyolite (Gibbon River flow), all of which erupted near the caldera margin ca. 100 ka. The Hayden Valley flow hosts two zircon populations and one sanidine population that are consistent with residence in the CPM reservoir. The Gibbon River flow hosts one zircon population that is compositionally distinct from Hayden Valley flow zircons. The Solfatara Plateau flow contains multiple sanidine populations and all three zircon populations found in the Hayden Valley and Gibbon River flows, demonstrating that the Solfatara Plateau flow formed by mixing extracaldera magma with the margin of the CPM reservoir. This process highlights the dynamic nature of magmatic interactions at the margins of large silicic reservoirs. More generally, Hf isotopic data from the CPM zircons provide the first direct evidence for isotopically juvenile magmas contributing mass to the youngest post-caldera magmatic system and demonstrate that the sources contributing magma to the CPM reservoir were heterogeneous in 176Hf/177Hf at ca. 100 ka. Thus, the limited compositional variability of CPM glasses reflects homogenization occurring within the CPM reservoir, not a homogeneous source.

  8. Asthenospheric and lithospheric sources for Mesozoic dolerites from Liberia (Africa): Trace element and isotopic evidence

    International Nuclear Information System (INIS)

    Dupuy, C.; Marsh, J.

    1988-01-01

    Combined elemental, and Sr and Nd isotopic data are presented for Mesozoic dolerite dikes of Liberia (Africa) which are related to the initial stage of opening of the Atlantic Ocean. The large scatter of both trace element and isotopic data allows the identification of five groups of dolerites which cannot be related to each other by simple processes of mineral fractionation from a common source. On the contrary, the observed chemical and isotopic variation within some dolerites (Groups I and II) may result either from variable degrees of melting of an isotopically heterogeneous source or mixing between enriched and depleted oceanic type mantle. For the other dolerites (Groups III-V) mixing with a third mantle source with more radiogenic Sr and with element ratios characteristic of subduction environments is suggested. This third source is probably the subcontinental lithospheric mantle. Finally, no significant modification by interaction with continental crust is apparent in most of the analyzed samples. (orig.)

  9. 23 Elemental Composition of Suspended Particulate Matter ...

    African Journals Online (AJOL)

    `123456789jkl''''#

    The samples were analysed by energy dispersive x-ray fluorescence. (EDXRF) and atomic absorption spectroscopy (AAS) for up to 10 elements. It was found that 66% of the ..... coefficients between the various crustal elements Ca, Ti, Mn, ...

  10. Isotopic composition and origin of the precipitation in Northern Chile

    International Nuclear Information System (INIS)

    Aravena, R.; Suzuki, O.; Pena, H.; Pollastri, A.; Fuenzalida, H.; Grilli, A.

    1999-01-01

    A 3 a data set of isotopes in precipitation from northern Chile show a very distinct pattern, with δ 18 O values ranging between -18 and -15per thousand at high altitude stations, compared to δ 18 O values between -10 and -6per thousand at the lower altitude areas. The 18 O-depleted values observed in the high altitude area, the Altiplano, are related to processes that affect the air masses that originated over the Atlantic, cross the Amazon Basin (continental effect), ascend the Andes (altitude effect) and precipitated (convective effect) in the Altiplano. It is postulated that a second source of moisture, associated with air masses from the Pacific, may contribute to the 18 O-enriched values observed in the lower altitude areas. Similar isotopic patterns are documented in springs and groundwater indicating that the data presented in this paper are an accurate representation of the long term behavior isotopic composition of rain in northern Chile. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

  11. Isotopic composition and origin of the precipitation in Northern Chile

    Energy Technology Data Exchange (ETDEWEB)

    Aravena, R. [Department of Earth Sciences, University of Waterloo, Waterloo (Canada); Suzuki, O. [Exploracion y Desarrollo de Recursos Hidricos, Santiago (Chile); Pena, H. [Direccion General de Aguas, Ministerio de Obras Publicas, Santiago (Chile); Pollastri, A. [Comision Chilena de Energia Nuclear, Santiago (Chile); Fuenzalida, H. [Departamento de Geofisica, Universidad of Chile, Santiago (Chile); Grilli, A. [Empresa Metropolitana de Obras Sanitarias, Santiago (Chile)

    1999-06-01

    A 3 a data set of isotopes in precipitation from northern Chile show a very distinct pattern, with {delta}{sup 18}O values ranging between -18 and -15per thousand at high altitude stations, compared to {delta}{sup 18}O values between -10 and -6per thousand at the lower altitude areas. The {sup 18}O-depleted values observed in the high altitude area, the Altiplano, are related to processes that affect the air masses that originated over the Atlantic, cross the Amazon Basin (continental effect), ascend the Andes (altitude effect) and precipitated (convective effect) in the Altiplano. It is postulated that a second source of moisture, associated with air masses from the Pacific, may contribute to the {sup 18}O-enriched values observed in the lower altitude areas. Similar isotopic patterns are documented in springs and groundwater indicating that the data presented in this paper are an accurate representation of the long term behavior isotopic composition of rain in northern Chile. (Copyright (c) 1999 Elsevier Science B.V., Amsterdam. All rights reserved.)

  12. The carbon isotope ratios and contents of mineral elements in leaves of Chinese medicinal plants

    International Nuclear Information System (INIS)

    Lin Zhifang; Sun Guchou; Wang Wei

    1989-01-01

    Leaf carbon isotope ratios and 13 kinds of mineral elements were measured on 36 species of common Chinese medicinal plants in a subtropical monsoon forest of Ding Hu Shan in Guangdong Province. The .delta.13C value were from -26.4 to -32.6%, indicating that all of the species belonged the photosynthetic C3 types. The relative lower value of δ13C was observed in the life form of shrubs. The contents of 7 elements (N, P, K, Ca, Na Mg, Si) were dependent upon the species, life form, medicinal function and medicinal part. Herb type medicine and the used medicinal part of leaves or whole plant showed higher levels of above elements than the others. Among the nine groups with different medicinal functions, it was found that more nitrogen was in the leaves of medicinal plants for hemophthisis, hypertension and stomachic troubles, more phosphorus and potassium were in the leaves for cancer and snake bite medicines, but more calcium and magnesium were in the leaves for curing rheumatics. Ferric, aluminium and manganese were the main composition of microelements in leaves. There were higher content of ferric in leaves for hemophthisis medicine, higher zinc in leaves for cold and hypertension medicine, and higher Cup in leaves of stomachic medicine. It was suggested that the pattern of mineral elements in leaves of Chinese medicinal plants reflected the different properties of absorption and accumulation. Some additional effect due to the high content of certain element might be associated with the main function of that medicine

  13. V isotope composition in modern marine hydrothermal sediments

    Science.gov (United States)

    Wu, F.; Owens, J. D.; Nielsen, S.; German, C. R.; Rachel, M.

    2017-12-01

    Vanadium is multivalence transition metal with two isotopes (51V and 50V). Recent work has shown that large V isotope variations occur with oxygen variations in modern sediments (Wu et al., 2016 and 2017 Goldschmidt Abstracts), providing its potential as a promising proxy for determining low oxygen conditions. However, the development of V isotopes as a proxy to probe past redox conditions requires a comprehensive understanding of the modern oceanic isotopic mass balance. Therein, the scavenging of V from the hydrous iron oxides in hydrothermal fluid has been shown to be an important removal process from seawater (Rudnicki and Elderfield, 1993 GCA) but remains unquantified. In this study, we analyzed V isotopic compositions of metalliferous sediments around the active TAG hydrothermal mound from the mid-Atlantic Ridge (26° degrees North) and the Eastern Pacific Zonal Transect (GEOTRACES EPZT cruise GP16). The TAG sediments deposited as Fe oxyhydroxides from plume fall-out, and have δ51V values between -0.3 to 0‰. The good correlation between Fe and V for these metalliferous sediments indicate that the accumulation of V in these samples is directly related to the deposition of Fe oxyhydroxides, which also control their V isotope signature. The EPZT samples cover 8,000 km in the South Pacific Ocean with sedimentary areas that underlie the Peru upwelling region and the well-oxygenated deep South Pacific Ocean influenced by hydtorthermal plume material from southern East Pacific Rise (EPR). The sediments collected at the east of the EPR have δ51V values between -1.2 to -0.7‰, similar to previous δ51V of oxic sediments. In contrast, the sediments from the west of the EPR have δ51V values (-0.4 to 0‰) similar to hydrothermal sediments from the mid-Atlantic Ridge, indicating the long transportation (more than 4,000 km, Fitzsimmons et al., 2017 NG) of Fe and Mn from hydrothermal plume and their incorporation into sediments have a major impact on the cycle of V

  14. Recent trends in accumulation rate, elemental and isotopic ...

    African Journals Online (AJOL)

    The isotope results show that the organic material deposited in the bay are generally derived from C4 type of plants and are not transported far from the river mouth. Also the results show that preservation of organic matter is high in open water probably due to high primary productivity owing to high concentration of nutrients ...

  15. Stable carbon isotopic composition of gasolines determined by isotope ratio monitoring gas chromatography mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Smallwood, B.J.; Philp, R.P.; Allen, J.D. [University of Oklahoma, Norman, OK (United States). School of Geology and Geophysics

    2002-07-01

    A large number of underground gasoline storage facilities in the United States continuously leak gasoline into the subsurface, which makes gasoline a major groundwater contaminant. Gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS) are used currently to characterize contaminated groundwater and soils. Correlations of contaminants with suspected source(s) are extremely difficult by these techniques because many gasolines have similar hydrocarbon distributions. The present study applied the technique of isotope ratio monitoring gas chromatography-mass spectrometry (irmGC-MS) to 19 gasoline samples from different areas of the USA. This allows a much better correlation of gasoline contaminants to source. Data obtained indicate a wide range of {sup {delta}}{sup 13}C values for 16 ubiquitous compounds in the gasolines. The majority of samples could be distinguished from each other on the basis of {sup {delta}}{sup 13}C hydrocarbon composition. The oxygenated additive methyl tertiary butyl ether (MTBE) was present in ten of the gasolines analyzed, and had a relatively narrow range of {sup {delta}}{sup 13}C values (-30.4 to -28.3 per mille). Preliminary investigations were also made to determine the extent of carbon isotopic fractionation after simple water washing and evaporation experiments. Results indicate that the majority of compounds did not undergo significant carbon isotopic fractionation as a result of these processes. (author)

  16. Composite elements with superconducting ceramic materials and preparation process

    International Nuclear Information System (INIS)

    Drifford, M.; Lambard, J.

    1990-01-01

    Supraconducting ceramic powder is introduced in a ductile metal with an open porosity, then the tube is sealed at both ends and necked to form a composite element which is sintered and the ceramic becomes superconductive by gaseous diffusion. Then the composite element can be placed into a gasproof cladding [fr

  17. Monitoring of carbon isotope composition of snow cover for Tomsk region

    Science.gov (United States)

    Akulov, P. A.; Volkov, Y. V.; Kalashnikova, D. A.; Markelova, A. N.; Melkov, V. N.; Simonova, G. V.; Tartakovskiy, V. A.

    2016-11-01

    This article shows the potential of using δ13C values of pollutants in snow pack to study the human impact on the environment of Tomsk and its surroundings. We believe that it is possible to use a relation between the isotope compositions of a fuel and black carbon for establishing the origin of the latter. The main object of our investigation was dust accumulated by the snow pack in the winter of 2015-2016. The study of dust samples included the following steps: determination of the total carbon content in snow pack samples of Tomsk and its surroundings, extraction of black carbon from the dust, as well as the determination of δ13C values of the total and black carbon accumulated in the snow pack. A snow survey was carried out on the 26th of January and on the 18th of March. The relative carbon content in the dust samples was determined by using an EA Flash 2000 element analyzer. It varied from 3 to 24%. The maximum carbon content was in the dust samples from areas of cottage building with individual heating systems. The δ13C values of the total and black carbon were determined by using a DELTA V Advantage isotope mass spectrometer (TomTsKP SB RAS). The isotope composition of black carbon corresponded to that of the original fuel. This fact allowed identifying the origin of black carbon in some areas of Tomsk.

  18. Stable-carbon isotopic composition of maple sap and foliage

    International Nuclear Information System (INIS)

    Leavitt, S.W.; Long, A.

    1985-01-01

    The 13 C/ 12 C ratios of Acer grandidentatum sap sugar collected during the dormant period are compared to those of buds, leaves, and wood developed over the following growing season. As the primary carbon source for cellulose manufacture at initiation of annual growth in deciduous trees, sap sucrose would be expected to have an isotopic composition similar to first-formed cellulose. Although constancy in concentration and 13 C/ 12 C ratios of the maple sap sugar suggests any gains or losses (e.g. to maintenance metabolism) do not appreciably alter composition, the 13 C/ 12 C ratios of cellulose of the enlarging buds in the spring are quite distinct from those of the sap sugar, seemingly precluding a simple direct biochemical pathway of sap sucrose→glucose→cellulose in favor of a more complex pathway with greater likelihood of isotopic fractionation. The 13 C/ 12 C ratios of the leaves and in the growth ring were initially similar to the sap sugar but decreased steadily over the growing season. (author)

  19. Elemental, isotopic, and structural changes in Tagish Lake insoluble organic matter produced by parent body processes

    Science.gov (United States)

    Alexander, C. M. O'd.; Cody, G. D.; Kebukawa, Y.; Bowden, R.; Fogel, M. L.; Kilcoyne, A. L. D.; Nittler, L. R.; Herd, C. D. K.

    2014-04-01

    Here, we present the results of a multitechnique study of the bulk properties of insoluble organic material (IOM) from the Tagish Lake meteorite, including four lithologies that have undergone different degrees of aqueous alteration. The IOM C contents of all four lithologies are very uniform and comprise about half the bulk C and N contents of the lithologies. However, the bulk IOM elemental and isotopic compositions vary significantly. In particular, there is a correlated decrease in bulk IOM H/C ratios and δD values with increasing degree of alteration—the IOM in the least altered lithology is intermediate between CM and CR IOM, while that in the more altered lithologies resembles the very aromatic IOM in mildly metamorphosed CV and CO chondrites, and heated CMs. Nuclear magnetic resonance (NMR) spectroscopy, C X-ray absorption near-edge (XANES), and Fourier transform infrared (FTIR) spectroscopy confirm and quantitate this transformation from CR-like, relatively aliphatic IOM functional group chemistry to a highly aromatic one. The transformation is almost certainly thermally driven, and probably occurred under hydrothermal conditions. The lack of a paramagnetic shift in 13C NMR spectra and 1s-σ* exciton in the C-XANES spectra, both typically seen in metamorphosed chondrites, shows that the temperatures were lower and/or the timescales were shorter than experienced by even the least metamorphosed type 3 chondrites. Two endmember models were considered to quantitatively account for the changes in IOM functional group chemistry, but the one in which the transformations involved quantitative conversion of aliphatic material to aromatic material was the more successful. It seems likely that similar processes were involved in producing the diversity of IOM compositions and functional group chemistries among CR, CM, and CI chondrites. If correct, CRs experienced the lowest temperatures, while CM and CI chondrites experienced similar more elevated temperatures

  20. Biomonitoring of trace metal elements by lichens of the Western Pyrenees.Study of elemental and isotopic signature of mercury

    OpenAIRE

    Queipo Abad, Silvia

    2012-01-01

    The lichens, organisms originated by symbiotic relationship between an algae and a fungus, have shown good properties as biomonitors of pollution from Trace Metal Elements. They can be used as indicators of local and long-range atmospheric pollution. The assessment of deposition of atmospheric pollutants results difficult to know their long term impact. This happens specially when the study is focalized in remote areas. In this project it has been developed the elemental and isotopic analy...

  1. Evolution of the Campanian Ignimbrite Magmatic System II: Trace Element and Th Isotopic Evidence for Open-System Processes

    Science.gov (United States)

    Bohrson, W. A.; Spera, F. J.; Fowler, S.; Belkin, H.; de Vivo, B.

    2005-12-01

    The Campanian Ignimbrite, a large volume (~200 km3 DRE) trachytic to phonolitic ignimbrite was deposited at ~39.3 ka and represents the largest of a number of highly explosive volcanic events in the region near Naples, Italy. Thermodynamic modeling of the major element evolution using the MELTS algorithm (see companion contribution by Fowler et al.) provides detailed information about the identity of and changes in proportions of solids along the liquid line of descent during isobaric fractional crystallization. We have derived trace element mass balance equations that explicitly accommodate changing mineral-melt bulk distribution coefficients during crystallization and also simultaneously satisfy energy and major element mass conservation. Although major element patterns are reasonably modeled assuming closed system fractional crystallization, modeling of trace elements that represent a range of behaviors (e.g. Zr, Nb, Th, U, Rb, Sm, Sr) yields trends for closed system fractionation that are distinct from those observed. These results suggest open-system processes were also important in the evolution of the Campanian magmatic system. Th isotope data yield an apparent isochron that is ~20 kyr younger than the age of the deposit, and age-corrected Th isotope data indicate that the magma body was an open-system at the time of eruption. Because open-system processes can profoundly change isotopic characteristics of a magma body, these results illustrate that it is critical to understand the contribution that open-system processes make to silicic magma bodies prior to assigning relevance to age or timescale information derived from isotope systematics. Fluid-magma interaction has been proposed as a mechanism to change isotopic and elemental characteristics of magma bodies, but an evaluation of the mass and thermal constraints on such a process suggest large-scale fluid-melt interaction at liquidus temperatures is unlikely. In the case of the magma body associated with

  2. Variability of Fe isotope compositions of hydrothermal sulfides and oxidation products at mid-ocean ridges

    Science.gov (United States)

    Li, Xiaohu; Wang, Jianqiang; Chu, Fengyou; Wang, Hao; Li, Zhenggang; Yu, Xing; Bi, Dongwei; He, Yongsheng

    2018-04-01

    Significant Fe isotopic fractionation occurs during the precipitation and oxidative weathering of modern seafloor hydrothermal sulfides, which has an important impact on the cycling of Fe isotopes in the ocean. This study reports the Fe-isotope compositions of whole-rock sulfides and single-mineral pyrite collected from hydrothermal fields at the South Mid-Atlantic Ridge (SMAR) and the East Pacific Rise (EPR) and discusses the impacts of precipitation and late-stage oxidative weathering of sulfide minerals on Fe isotopic fractionation. The results show large variation in the Fe-isotope compositions of the sulfides from the different hydrothermal fields on the mid-oceanic ridges, indicating that relatively significant isotope fractionation occurs during the sulfide precipitation and oxidative weathering processes. The Fe-isotope compositions of the sulfides from the study area at the SMAR vary across a relatively small range, with an average value of 0.01‰. This Fe-isotope composition is similar to the Fe-isotope composition of mid-oceanic ridge basalt, which suggests that Fe was mainly leached from basalt. In contrast, the Fe-isotope composition of the sulfides from the study area at the EPR are significantly enriched in light Fe isotopes (average value - 1.63‰), mainly due to the kinetic fractionation during the rapid precipitation process of hydrothermal sulfide. In addition, the pyrite from different hydrothermal fields is enriched in light Fe isotopes, which is consistent with the phenomenon in which light Fe isotopes are preferentially enriched during the precipitation of pyrite. The red oxides have the heaviest Fe-isotope compositions (up to 0.80‰), indicating that heavy Fe isotopes are preferentially enriched in the oxidation product during the late-stage oxidation process. The data obtained from this study and previous studies show a significant difference between the Fe-isotope compositions of the sulfides from the SMAR and EPR. The relatively heavy

  3. The precise measurement of TL isotopic compositions by MC-ICPMS: Application to the analysis of geological materials and meteorites.

    Science.gov (United States)

    Rehkämper, Mark; Halliday, Alex N.

    1999-07-01

    scavenging from seawater. Thallium is the heaviest element for which such a natural isotopic fractionation has been verified. For a bulk sample of the C3V chondrite Allende we have determined a Tl isotopic composition of ɛ Tl = -2.1 ± 1.4, the lowest value measured in this study. By combining our data for Allende with a previously published Tl isotopic composition for the L3 chondrite Mezö-Madaras we obtain an upper limit of 9.2 × 10 -5 for the 205Pb/ 204Pb abundance ratio of the bulk solar system at the time of volatile element depletion. If the chemical depletion of volatile elements occurred early, during the condensation of the solar nebula, our result would indicate that the initial Solar System abundance of 205Pb is significantly lower than some current astrophysical estimates.

  4. Reference and intercomparison materials for stable isotopes of light elements. Proceedings of a consultants meeting held in Vienna, 1-3 December 1993

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-09-01

    The stable isotope composition of elements varies in natural compounds as a consequence of the slightly different physico-chemical behaviour of isotopes. The possibility of measuring the stable isotope relative variations with high precision, using mass spectrometry, promoted the rise of new fields of research in geochemistry and hydrology and, more recently, in environmental studies. The steady growth of these investigations and of their practical applications has emphasized the need for high quality isotopic standards and intercomparison samples, with well determined isotopic composition, for the intercalibration of analytical techniques and results among laboratories. The organization of the Consultants Meeting on Stable Isotope Standards and Intercomparison Materials held in Vienna from 1 to 3 December 1993, the fifth of this type (the previous meetings took place in 1966, 1976, 1983 and 1985), called for a review and a discussion of the characteristics, quality and availability of the existing standards and intercalibration materials, and for an assessment of needs for new materials, in view of recent developments and applications. A large part of the discussions was devoted to the new materials prepared for sulphur isotope analysis and the analytical requirements for highly precise isotopic analysis of CO{sub 2}. The papers presented at the meeting are assembled in this volume. Refs, figs and tabs.

  5. Reference and intercomparison materials for stable isotopes of light elements. Proceedings of a consultants meeting held in Vienna, 1-3 December 1993

    International Nuclear Information System (INIS)

    1995-09-01

    The stable isotope composition of elements varies in natural compounds as a consequence of the slightly different physico-chemical behaviour of isotopes. The possibility of measuring the stable isotope relative variations with high precision, using mass spectrometry, promoted the rise of new fields of research in geochemistry and hydrology and, more recently, in environmental studies. The steady growth of these investigations and of their practical applications has emphasized the need for high quality isotopic standards and intercomparison samples, with well determined isotopic composition, for the intercalibration of analytical techniques and results among laboratories. The organization of the Consultants Meeting on Stable Isotope Standards and Intercomparison Materials held in Vienna from 1 to 3 December 1993, the fifth of this type (the previous meetings took place in 1966, 1976, 1983 and 1985), called for a review and a discussion of the characteristics, quality and availability of the existing standards and intercalibration materials, and for an assessment of needs for new materials, in view of recent developments and applications. A large part of the discussions was devoted to the new materials prepared for sulphur isotope analysis and the analytical requirements for highly precise isotopic analysis of CO 2 . The papers presented at the meeting are assembled in this volume. Refs, figs and tabs

  6. Continuous measurements of isotopic composition of water vapour on the East Antarctic Plateau

    Directory of Open Access Journals (Sweden)

    M. Casado

    2016-07-01

    Full Text Available Water stable isotopes in central Antarctic ice cores are critical to quantify past temperature changes. Accurate temperature reconstructions require one to understand the processes controlling surface snow isotopic composition. Isotopic fractionation processes occurring in the atmosphere and controlling snowfall isotopic composition are well understood theoretically and implemented in atmospheric models. However, post-deposition processes are poorly documented and understood. To quantitatively interpret the isotopic composition of water archived in ice cores, it is thus essential to study the continuum between surface water vapour, precipitation, surface snow and buried snow. Here, we target the isotopic composition of water vapour at Concordia Station, where the oldest EPICA Dome C ice cores have been retrieved. While snowfall and surface snow sampling is routinely performed, accurate measurements of surface water vapour are challenging in such cold and dry conditions. New developments in infrared spectroscopy enable now the measurement of isotopic composition in water vapour traces. Two infrared spectrometers have been deployed at Concordia, allowing continuous, in situ measurements for 1 month in December 2014–January 2015. Comparison of the results from infrared spectroscopy with laboratory measurements of discrete samples trapped using cryogenic sampling validates the relevance of the method to measure isotopic composition in dry conditions. We observe very large diurnal cycles in isotopic composition well correlated with temperature diurnal cycles. Identification of different behaviours of isotopic composition in the water vapour associated with turbulent or stratified regime indicates a strong impact of meteorological processes in local vapour/snow interaction. Even if the vapour isotopic composition seems to be, at least part of the time, at equilibrium with the local snow, the slope of δD against δ18O prevents us from identifying

  7. Spectroscopic metrology for isotope composition measurements and transfer standards

    Science.gov (United States)

    Anyangwe Nwaboh, Javis; Balslev-Harder, David; Kääriäinen, Teemu; Richmond, Craig; Manninen, Albert; Mohn, Joachim; Kiseleva, Maria; Petersen, Jan C.; Werhahn, Olav; Ebert, Volker

    2017-04-01

    The World Meteorological Organization (WMO) has identified greenhouse gases such as CO2, CH4 and N2O as critical for global climate monitoring. Other molecules such as CO that has an indirect effect of enhancing global warming are also monitored. WMO has stated compatibility goals for atmospheric concentration and isotope ratio measurements of these gases, e.g. 0.1 ppm for CO2 concentration measurements in the northern hemisphere and 0.01 ‰ for δ13C-CO2. For measurements of the concentration of greenhouse gases, gas analysers are typically calibrated with static gas standards e.g. traceable to the WMO scale or to the International System of Units (SI) through a national metrology institute. However, concentrations of target components, e.g. CO, in static gas standards have been observed to drift, and typically the gas matrix as well as the isotopic composition of the target component does not always reflect field gas composition, leading to deviations of the analyser response, even after calibration. The deviations are dependent on the measurement technique. To address this issue, part of the HIGHGAS (Metrology for high-impact greenhouse gases) project [1] focused on the development of optical transfer standards (OTSs) for greenhouse gases, e.g. CO2 and CO, potentially complementing gas standards. Isotope ratio mass spectrometry (IRMS) [2] is currently used to provide state-of-the-art high precision (in the 0.01 ‰ range) measurements for the isotopic composition of greenhouse gases. However, there is a need for field-deployable techniques such as optical isotope ratio spectroscopy (OIRS) that can be combined with metrological measurement methods. Within the HIGHGAS project, OIRS methods and procedures based on e.g. cavity enhanced spectroscopy (CES) and tunable diode laser absorption spectroscopy (TDLAS), matched to metrological principles have been established for the measurement of 13C/12C and 18O/16O ratios in CO2, 15N/14N ratios in N2O, and 13C/12C and 2H

  8. Heterogeneity of the Caribbean plateau mantle source: Sr, O and He isotopic compositions of olivine and clinopyroxene from Gorgona Island

    Science.gov (United States)

    Révillon, S.; Chauvel, C.; Arndt, N. T.; Pik, R.; Martineau, F.; Fourcade, S.; Marty, B.

    2002-12-01

    The composition of the mantle plumes that created large oceanic plateaus such as Ontong Java or the Caribbean is still poorly known. Geochemical and isotopic studies on accreted portions of the Caribbean plateau have shown that the plume source was heterogeneous and contained isotopically depleted and relatively enriched portions. A distinctive feature of samples from the Caribbean plateau is their unusual Sr isotopic compositions, which, at a given Nd isotopic ratio, are far higher than in samples from other oceanic plateaus. Sr, O and He isotopic compositions of whole rocks and magmatic minerals (clinopyroxene or olivine) separated from komatiites, gabbros and peridotites from Gorgona Island in Colombia were determined to investigate the origin of these anomalously radiogenic compositions. Sequentially leached clinopyroxenes have Sr isotopic compositions in the range 87Sr/ 86Sr=0.70271-0.70352, systematically lower than those of leached and unleached whole rocks. Oxygen isotopic ratios of clinopyroxene vary within the range δ 18O=5.18-5.35‰, similar to that recorded in oceanic island basalts. He isotopic ratios are high ( R/ Ra=8-19). The lower 87Sr/ 86Sr ratios of most of the clinopyroxenes shift the field of the Caribbean plateau in Nd-Sr isotope diagrams toward more 'normal' values, i.e. a position closer to the field defined by mid-ocean ridge basalts and oceanic-island basalts. Three clinopyroxenes have slightly higher 87Sr/ 86Sr ratios that cannot be explained by an assimilation model. The high 87Sr/ 86Sr and variations of 143Nd/ 144Nd are interpreted as a source characteristic. Trace-element ratios, however, are controlled mainly by fractionation during partial melting. We combine these isotopic data in a heterogeneous plume source model that accounts for the diversity of isotopic signatures recorded on Gorgona Island and throughout the Caribbean plateau. The heterogeneities are related to old recycled oceanic lithosphere in the plume source; the high 3

  9. Seasonality of Leaf Carbon Isotopic Composition and Leaf Water Isotopic Enrichment in a Mixed Evergreen Forest in Southern California

    Science.gov (United States)

    Santiago, L. S.; Sickman, J. O.; Goulden, M.; DeVan, C.; Pasquini, S. C.; Pivovaroff, A. L.

    2011-12-01

    Leaf carbon isotopic composition and leaf water isotopic enrichment reflect physiological processes and are important for linking local and regional scale processes to global patterns. We investigated how seasonality affects the isotopic composition of bulk leaf carbon, leaf sugar carbon, and leaf water hydrogen under a Mediterranean climate. Leaf and stem samples were collected monthly from four tree species (Calocedrus decurrens, Pinus lambertiana, Pinus ponderosa, and Quercus chrysolepis) at the James San Jacinto Mountain Reserve in southern California. Mean monthly bulk leaf carbon isotopic composition varied from -34.5 % in P. ponderosa to -24.7 % in P. lambertiana and became more depleted in 13C from the spring to the summer. Mean monthly leaf sugar varied from -29.3 % in P. ponderosa to -21.8 % in P. lambertiana and was enriched in 13C during the winter, spring and autumn, but depleted during the mid-summer. Leaf water hydrogen isotopic composition was 28.4 to 68.8 % more enriched in deuterium than source water and this enrichment was greater as seasonal drought progressed. These data indicate that leaf carbon and leaf water hydrogen isotopic composition provide sensitive measures that connect plant physiological processes to short-term climatic variability.

  10. Pb isotopic composition of the atmosphere of the Sao Paulo city, Brazil, and isotopic characterization of some pollutant sources

    International Nuclear Information System (INIS)

    Aily, C.; Babinski, M.; Ruiz, I.R.; Sato, K

    2001-01-01

    Lead isotopes are known to be good tools for surveying lead origin in atmospheric samples (Chow et al., 1975). Lead has four naturally occurring stable isotopes: 206 Pb, 207 Pb, 208 Pb and 204 Pb. The first three isotopes are end products of radioactive decay chains from 238 U, 235 U and 232 Th, respectively, and the last one is non-radiogenic. Therefore, their abundance and the ratios among the four isotopes gradually change with time. Lead in the atmosphere comes from various sources, such as leaded gasoline, industrial emissions and coal combustion. Thus, lead isotope ratios different from those of the mother rock in the region are often observed in the atmosphere (Tatsumoto and Patterson, 1963). Lead is emitted to the atmosphere in fine particles, which can be transported within air masses for very long distances, e. g. from mid latitude regions to the Artic and Antarctica (Sturges and Barrie, 1989). Lead isotopes have been used to trace the pollutant sources in many cities of the world. However, a systematic study using this methodology has not been done in any Brazilian city. The main purpose of the present work is to characterize the Pb isotope composition in the atmosphere in Sao Paulo city, and suggest the possible pollutant sources. For our study lead isotopes were measured in different samples: aerosols and rainwater which would yield the Pb isotope composition of the atmosphere. Samples of gasoline and ethanol, gutter sweepings, soot from vehicle exhaust pipes, and filters containing particulate material from industrial emissions were also analyzed, since they were considered potential pollutant sources of the atmosphere. In order to obtain the local geogenic Pb isotopic composition we also analyzed rock and K-feldspar samples. Lead concentrations were only determined on aerosols and rainwater samples (au)

  11. Barium isotopes in Allende meteorite - Evidence against an extinct superheavy element

    Science.gov (United States)

    Lewis, R. S.; Anders, E.; Shimamura, T.; Lugmair, G. W.

    1983-01-01

    Carbon and chromite fractions from the Allende meteorite that contain isotopically anomalous xenon-131 to xenon-136 (carbonaceous chondrite fission or CCF xenon) at up to 5 x 10 to the 11th atoms per gram show no detectable isotopic anomalies in barium-130 to barium-138. This rules out the possibility that the CCF xenon was formed by in situ fission of an extinct superheavy element. Apparently the CCF xenon and its carbonaceous carrier are relics from stellar nucleosynthesis.

  12. Variations in Urine Calcium Isotope: Composition Reflect Changes in Bone Mineral Balance in Humans

    Science.gov (United States)

    Skulan, Joseph; Anbar, Ariel; Bullen, Thomas; Puzas, J. Edward; Shackelford, Linda; Smith, Scott M.

    2004-01-01

    Changes in bone mineral balance cause rapid and systematic changes in the calcium isotope composition of human urine. Urine from subjects in a 17 week bed rest study was analyzed for calcium isotopic composition. Comparison of isotopic data with measurements of bone mineral density and metabolic markers of bone metabolism indicates the calcium isotope composition of urine reflects changes in bone mineral balance. Urine calcium isotope composition probably is affected by both bone metabolism and renal processes. Calcium isotope. analysis of urine and other tissues may provide information on bone mineral balance that is in important respects better than that available from other techniques, and illustrates the usefulness of applying geochemical techniques to biomedical problems.

  13. Determination of isotope ratio of elements by mass distribution in molecules of varied chemical compounds

    International Nuclear Information System (INIS)

    Gladkikh, I.S.; Babichev, A.P.

    1999-01-01

    The procedure and program for calculation of isotope ratio of elements involving in the compound being studied using data of mass spectrometry were elaborated. The methods developed for the O 2 , SiH 4 , Cd(CH 3 ) 2 molecules were demonstrated for the illustration. The results of calculation provide support for the efficiency of the program and satisfactory reliability of the results during calculation of the isotope and complex compound concentrations. The program may be used for the estimation of the degree of nonequilibrium isotope distributions, it may indicate on the errors of the mass spectroscopy results [ru

  14. Isotope ratio analysis by a combination of element analyzer and mass spectrometer

    International Nuclear Information System (INIS)

    Pichlmayer, F.

    1987-06-01

    The use of stable isotope ratios of carbon, nitrogen and sulfur as analytical tool in many fields of research is of growing interest. A method has therefore been developed, consisting in essential of coupling an Elemental Analyzer with an Isotope Mass Spectrometer, which enables the gas preparation of carbon dioxide, nitrogen and sulfur dioxide from any solid or liquid sample in a fast and easy way. Results of carbon isotope measurements in food analysis are presented, whereat it is possible to check origin and treatment of sugar, oils, fats, mineral waters, spirituous liquors etc. and to detect adulterations as well. Also applications in the field of environmental research are given. (Author)

  15. Isotopic and elemental proxies in mollusc and brachiopod calcite

    DEFF Research Database (Denmark)

    Ullmann, Clemens Vinzenz

    composition of the oceans have changed. These changes of environmental conditions and seawater composition are primarily caused by plate tectonic processes, the cyclic variations of the Earth’s orbital parameters and living organisms, actively causing, and passively adapting to shifting conditions...

  16. Correlated silicon and titanium isotopic compositions of presolar SiC grains from the Murchison CM2 chondrite

    Science.gov (United States)

    Gyngard, Frank; Amari, Sachiko; Zinner, Ernst; Marhas, Kuljeet Kaur

    2018-01-01

    We report correlated Si, and Ti isotopic compositions and elemental concentrations of 238 presolar SiC grains from the Murchison CM2 meteorite. Combined with measurements of the C and N isotopic compositions of these 238 grains, 220 were determined to be of type mainstream, 10 type AB, 4 type Y and 4 type Z. SiC grains of diameter ≳2.5 μm, to ensure enough material to attempt Ti measurements, were randomly chosen without any other prejudice. The Ti isotopic compositions of the majority of the grains are characterized by enrichments in 46Ti, 47Ti, 49Ti, and 50Ti relative to 48Ti, and show linear isotopic correlations indicative of galactic chemical evolution and neutron capture of the grains parent stars. The variability in the observed Ti signal as a function of depth in most of the grains indicates the presence of distinct subgrains, likely TiC that have been previously observed in TEM studies. Vandium-51 concentrations correlate with those of Ti, indicating V substitutes for Ti in the TiC matrix in many of the grains. No isotopic anomalies in 52Cr/53Cr ratios were observed, and Cr concentrations did not correlate with those of either Ti or V.

  17. Isotopic and trace element constraints on the genesis of a boninitic sequence in the Thetford Mines ophiolitic complex, Quebec, Canada

    International Nuclear Information System (INIS)

    Olive, V.; Hebert, R.; Loubet, M.

    1997-01-01

    The Mont Ham Massif (part of the Thetford Mines ophiolite, south Quebec) represents a magmatic sequence made up of tholeiitic and boninitic derived products. A geochemical study confirms the multicomponent mixing models that have been classically advanced for the source of boninites, with slab-derived components added to the main refractory harzburgitic peridotite. An isochron diagram of the boninitic rocks is interpreted as a mixing trend between two components: (i) a light rare earth element (LREE) enriched component (A), interpreted as slab-derived fluid-melts equilibrated with sedimentary materials (ε Nd = -3, 147 Sm/ 144 Nd = 0.140), and (ii) a LREE-depleted component (B) (0.21 147 Sm/ 144 Nd Nd = 9). A multicomponent source is also necessary to explain the Nd-isotope and trace element composition of the tholeiites, which are explained by the melting of a more fertile, Iherzolitic mantle and (or) mid-ocean ridge basalt source (component C), characterized by a large-ion lithophile element depicted pattern and an lapetus mantle Nd isotopic composition (ε Nd = 9), mixed in adequate proportions with the two previously infered slab-derived components (A and B). The genesis of the boninites of Mont Ham is not significantly different from those of boninites located in the Pacific. An intraoceanic subduction zone appears to be an appropriate geodynamic environment for the Mont Ham ophiolitic sequence. (author)

  18. Characteristics of trace elements and lead isotope ratios in PM2.5 from four sites in Shanghai

    International Nuclear Information System (INIS)

    Chen Jianmin; Tan Mingguang; Li Yulan; Zheng Jian; Zhang Yuanmao; Shan Zuci; Zhang Guilin; Li Yan

    2008-01-01

    PM 2.5 samples were collected in Shanghai at four sites with different typical land-uses. The sampling was done concurrently once per month from April 2004 to April 2005, and the ambient mass concentration, the elemental composition and the stable lead isotope ratios in these PM 2.5 samples were determined. The annual average concentrations of PM 2.5 samples at each site were 84 ± 30, 65 ± 20, 55 ± 18, and 41 ± 10 μg m -3 , respectively, indicating there were severe air pollution levels in Shanghai. The enrichment factor was calculated for each element and the comparison and discussion of elements with significant anthropogenic contributions between Shanghai and Tokyo suggested that the major source of PM 2.5 in Shanghai was not traffic-derived emissions, but the stationary industrial contribution emitted from coal use. Moreover, the analysis of stable lead isotope ratios revealed only a slight difference within the samples at the four sites which fell well within the scope of coal composition difference, further confirming that the contribution from stationary industrial emissions to atmospheric lead pollution of PM 2.5 was very substantial in Shanghai

  19. Neutron-rich isotopes of the lightest elements

    International Nuclear Information System (INIS)

    Oganesyan, Yu.Ts.; Penionzhkevich, Yu.Eh.; Kalpakchieva, R.

    1989-01-01

    A review is presented of the experimental investigations on the stability of very neutron-rich light nuclei carried out at the JINR Laboratory of Nuclear Reactions. Results on mass excess measurements are reported for 4 H, 5 H, 6 H, 7 H and for the superheavy helium isotope 9 He. Some results from the joint JINR-Ganil experiment on the search for and study of new neutron-rich light nuclei are also given. Analyzed are new possibilities for the investigation of multineutron decay of light nuclei. 14 refs.; 10 figs

  20. Evolution of the hafnium isotopic composition in the RBMK reactor

    International Nuclear Information System (INIS)

    Jurkevicius, A.; Remeikis, V.

    2002-01-01

    The isotopic composition of hafnium in the radial neutron flux sensor of the RBMK-1500 reactor, the rates of the neutron absorption on Hf isotopes and the neutron spectrum in the sensor were numerically modeled. The sequence SAS2 (Shielding Analysis Sequence) program from the package SCALE 4.4A and the HELIOS code system were used for calculations. It has been obtained that the overall neutron absorption rates in hafnium for the sensors located in the 2.4 % and 2.6 % enrichment uranium-erbium nuclear fuel assemblies are by 16 % and 19 % lower than in the 2.0 % enrichment uranium nuclear fuel assemblies. The overall neutron absorption rate in hafnium decreases 2.70-2.75 times due to the sensor burnup to 5800 MW d. The sensitivity of the Hf sensors to the thermal neutron flux increases twice due to the nuclear fuel assembly burnup to 3000 MW d. The corrective factors ξ d (I) at the different integral current I of the sensors and ξ td (E) at the different burnup E of the nuclear fuel assemblies were calculated. The obtained dependence ξ d (I) calculated numerically was compared to the experimental one determined by comparing signals of the fresh sensor and the sensor with the integral current I and by processing repeated calibration results of Hf sensors in RBMK-1500 reactors. The relative relationship coefficients K T (T FA ) were found for all RBMK-1500 nuclear fuel types. (author)

  1. Carbon-13 and oxygen-18 isotope effects in the decarboxylation of nicotinic acid of natural isotopic composition

    International Nuclear Information System (INIS)

    Zielinski, M.; Zielinska, A.; Papiernik-Zielinska, H.; McKenzie, J.A.; Bernasconi, S.; Paul, H.

    1998-01-01

    Carbon-13 and oxygen-18 isotope effects in the decarboxylation of nicotinic acid of natural isotopic composition above and below its melting temperature have been studied and compared with the primary (PKIE) and secondary kinetic isotope effects (SKIE) of 13 C and 18 O, respectively, in the decarboxylation of other heterocyclic acids. The temperature dependence of the secondary oxygen-18 isotope effects is negative in the total 221-255 deg C temperature interval investigated initially. The 13 C KIE measured above melting point of N.A. (temperature interval 235-270 deg C) are located in the range 1.007-1.009. Below melting point of nicotinic acid the 13 C KIE are larger and reveal the negative temperature dependence ( 13 C KIE decreases with decreasing the reaction temperature from 1.013/at 230 deg C to 1.0114/at 221 deg C). A discussion of the above isotopic results is presented. (author)

  2. The method and program system CABEI for adjusting consistency between natural element and its isotopes data

    Energy Technology Data Exchange (ETDEWEB)

    Tingjin, Liu; Zhengjun, Sun [Chinese Nuclear Data Center, Beijing, BJ (China)

    1996-06-01

    To meet the requirement of nuclear engineering, especially nuclear fusion reactor, now the data in the major evaluated libraries are given not only for natural element but also for its isotopes. Inconsistency between element and its isotopes data is one of the main problem in present evaluated neutron libraries. The formulas for adjusting to satisfy simultaneously the two kinds of consistent relationships were derived by means of least square method, the program system CABEI were developed. This program was tested by calculating the Fe data in CENDL-2.1. The results show that adjusted values satisfy the two kinds of consistent relationships.

  3. New isotopes of elements 104, 106 and 108 - highly stable superheavy nuclei

    International Nuclear Information System (INIS)

    Oganessian, Yuri

    1994-01-01

    In April 1993, as part of a joint Dubna-Livermore experiment at the Flerov Laboratory of Nuclear Reactions, new heavy isotopes of elements 104 and 106 were synthesized - 262 104, 265 106 and 266 106. Compared with the known even-even isotopes of elements 104 and 106, the new nuclei are characterized by their extraordinary high resistance to spontaneous fission. This is a direct proof of the macro-microscopic theory predictions in its version calculated by A.Sobiczewski et al. regarding a substantial increase in the half-lives of heavy nuclei near deformed shells with atomic number (Z) 108 and neutron number (N) 162.

  4. Comparison of the concentrations of metal elements and isotopes of lead found in rice and rice bran.

    Science.gov (United States)

    Dai, Shouhui; Yang, Hui; Yang, Lan; Wang, Fuhua; Du, Ruiying; Wen, Dian

    2014-08-01

    Very few studies have investigated the difference in the distribution of metal elements between rice and rice bran samples. In this study, the concentrations of 27 metal elements (Li, Be, Na, Mg, Al, K, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Ag, Cd, Cs, Ba, Tl, Pb, and U) in 56 polished rice and their corresponding bran samples were determined. A significant difference in concentrations of all elements except Ag and Cd was found between rice and bran (P rice ratios of 1.21 to 36.3. High concentrations of metal elements, especially that of the heavy metal Cr, in bran samples present a potential safety issue for bran products, such as food and feed containing bran. Pb isotope ((204)Pb, (206)Pb, (207)Pb, and (208)Pb) ratios also were determined. The (206)Pb/(207)Pb and (208)Pb/(207)Pb ratios in bran were generally higher than those in rice (P rice and bran samples were distinctly different from each other, indicating that Pb isotope composition is an effective for discriminating between bran and rice samples.

  5. The isotopic composition of CO in vehicle exhaust

    Science.gov (United States)

    Naus, S.; Röckmann, T.; Popa, M. E.

    2018-03-01

    We investigated the isotopic composition of CO in the exhaust of individual vehicles. Additionally, the CO2 isotopes, and the CO:CO2, CH4:CO2 and H2:CO gas ratios were measured. This was done under idling and revving conditions, and for three vehicles in a full driving cycle on a testbench. The spread in the results, even for a single vehicle, was large: for δ13 C in CO ∼ -60 to 0‰, for δ18 O in CO ∼ +10 to +35‰, and for all gas ratios several orders of magnitude. The results show an increase in the spread of isotopic values for CO compared to previous studies, suggesting that increasing complexity of emission control in vehicles might be reflected in the isotopic composition. When including all samples, we find a weighted mean for the δ13 C and δ18 O in CO of -28.7 ± 0.5‰ and +24.8 ± 0.3‰ respectively. This result is dominated by cold petrol vehicles. Diesel vehicles behaved as a distinct group, with CO enriched in 13C and depleted in 18O, compared to petrol vehicles. For the H2:CO ratio of all vehicles, we found a value of 0.71 ± 0.31 ppb:ppb. The CO:CO2 ratio, with a mean of 19.4 ± 6.8 ppb:ppm, and the CH4:CO2 ratio, with a mean of 0.26 ± 0.05 ppb:ppm, are both higher than recent literature indicates. This is likely because our sampling distribution was biased towards cold vehicles, and therefore towards higher emission situations. The CH4:CO2 ratio was found to behave similarly to the CO:CO2 ratio, suggesting that the processes affecting CO and CH4 are similar. The δ13 C values in CO2 were close to the expected δ13 C in fuel, with no significant difference between petrol and diesel vehicles. The δ18 O values in CO2 for petrol vehicles covered a range of 20-35‰, similar to the δ18 O of CO. The δ18 O values in CO2 for diesel vehicles were close to the δ18 O in atmospheric oxygen. A set of polluted atmospheric samples, taken near a highway and inside parking garages, showed an isotopic signature of CO and a H2:CO ratio that were

  6. Measurement of isotopic composition of lanthanides in reprocessing process solutions by high-performance liquid chromatography with inductively coupled plasma mass spectrometry (HPLC/ICP-MS)

    International Nuclear Information System (INIS)

    Okano, Masanori; Jitsukata, Shu; Kuno, Takehiko; Yamada, Keiji

    2011-01-01

    Isotopic compositions of fission products in process solutions and wastes in a reprocessing plant are valuable to proceed safety study of the solutions and research/development concerning treatment/disposal of the wastes. The amount of neodymium-148 is a reliable indication to evaluate irradiation history. The isotopic compositions of samarium and gadolinium in high radioactive wastes are referred to as essential data to evaluate environmental impact in geological repositories. However, pretreatment of analysis must be done with complicated chemical separation such as solvent extraction and ion exchange. The actual measurement data of isotopic compositions of lanthanides comparable to the one of actinides in spent fuel reprocessing process has not been obtained enough. Rapid and high sensitive analytical technique based on high-performance liquid chromatography (HPLC) with an inductively coupled plasma mass spectrometry (ICP-MS) has been developed for the measurement of isotopic compositions of lanthanides in spent fuel reprocessing solutions. HPLC/ICP-MS measurement system was customized for a glove-box to be applied to the radioactive solutions. The cation exchange chromatographic columns (Shim-pack IC-C1) and injection valve (20μL) were located inside of the glove-box except the chromatographic pump. The elements of lanthanide group were separated by a gradient program of HPLC with α-hydroxyisobutyric acid. Isotopic compositions of lanthanides in eluate was sequentially analyzed by a quadruple ICP-MS. Optimization of parameter of HPLC and ICP-MS measurement system was examined with standard solutions containing 14 lanthanide elements. The elements of lanthanides were separated by HPLC and detected by ICP-MS within 25 minutes. The detection limits of Nd-146, Sm-147 and Gd-157 were 0.37 μg L -1 , 0.69 μg L -1 and 0.47 μg L -1 , respectively. The analytical precision of the above three isotopes was better than 10% for standard solutions of 100 μg L -1 with

  7. Abnormal lithium isotope composition from the ancient lithospheric mantle beneath the North China Craton.

    Science.gov (United States)

    Tang, Yan-Jie; Zhang, Hong-Fu; Deloule, Etienne; Su, Ben-Xun; Ying, Ji-Feng; Santosh, M; Xiao, Yan

    2014-03-04

    Lithium elemental and isotopic compositions of olivines in peridotite xenoliths from Hebi in the North China Craton provide direct evidence for the highly variable δ(7)Li in Archean lithospheric mantle. The δ(7)Li in the cores of olivines from the Hebi high-Mg# peridotites (Fo > 91) show extreme variation from -27 to +21, in marked deviation from the δ(7)Li range of fresh MORB (+1.6 to +5.6) although the Li abundances of the olivines are within the range of normal mantle (1-2 ppm). The Li abundances and δ(7)Li characteristics of the Hebi olivines could not have been produced by recent diffusive-driven isotopic fractionation of Li and therefore the δ(7)Li in the cores of these olivines record the isotopic signature of the subcontinental lithospheric mantle. Our data demonstrate that abnormal δ(7)Li may be preserved in the ancient lithospheric mantle as observed in our study from the central North China Craton, which suggest that the subcontinental lithospheric mantle has experienced modification of fluid/melt derived from recycled oceanic crust.

  8. 0 Elemental Composition of Atmospheric Particulate Matter during ...

    African Journals Online (AJOL)

    Michael Horsfall

    ABSTRACT: The elemental composition of PM10 was studied during 2006 wet season in a rural background ... reference of crustal material, showed that for the coarse size fraction, most .... particular sector was made using criteria similar to.

  9. Validation of multi-element isotope dilution ICPMS for the analysis of basalts

    Energy Technology Data Exchange (ETDEWEB)

    Willbold, M.; Jochum, K.P.; Raczek, I.; Amini, M.A.; Stoll, B.; Hofmann, A.W. [Max-Planck-Institut fuer Chemie, Mainz (Germany)

    2003-09-01

    In this study we have validated a newly developed multi-element isotope dilution (ID) ICPMS method for the simultaneous analysis of up to 12 trace elements in geological samples. By evaluating the analytical uncertainty of individual components using certified reference materials we have quantified the overall analytical uncertainty of the multi-element ID ICPMS method at 1-2%. Individual components include sampling/weighing, purity of reagents, purity of spike solutions, calibration of spikes, determination of isotopic ratios, instrumental sources of error, correction of mass discrimination effect, values of constants, and operator bias. We have used the ID-determined trace elements for internal standardization to improve indirectly the analysis of 14 other (mainly mono-isotopic trace elements) by external calibration. The overall analytical uncertainty for those data is about 2-3%. In addition, we have analyzed USGS and MPI-DING geological reference materials (BHVO-1, BHVO-2, KL2-G, ML3B-G) to quantify the overall bias of the measurement procedure. Trace element analysis of geological reference materials yielded results that agree mostly within about 2-3% relative to the reference values. Since these results match the conclusions obtained by the investigation of the overall analytical uncertainty, we take this as a measure for the validity of multi-element ID ICPMS. (orig.)

  10. Elemental composition of commercial sea cucumbers (holothurians).

    Science.gov (United States)

    Wen, J; Hu, C

    2010-01-01

    Toxic and essential elements in 11 different sea cucumber species were determined and compared with daily intake recommendations and maximum allowed levels. The contents of macro-elements contents in dried sea cucumber samples were found to be 25,000-152,000 mg kg(-1) for Na, 4000-8600 mg kg(-1) for Mg, 1100-5200 mg kg(-1) for K, 15,000-68,000 mg kg(-1) and 36,300-251,000 mg kg(-1) for Cl. Trace element concentrations in dried sea cucumber samples were found to be 11-100 mg kg(-1) for Zn, 41-660 mg kg(-1) for Fe, 3-74 mg kg(-1) for Cu, 1.1-16 mg kg(-1) for Mn, 1.4-3.7 mg kg(-1) for Se, 1.1-9.6 mg kg(-1) for Cr, and 0.3-5.1 mg kg(-1) for Ni. All sea cucumber species were rich sources of Na, Cl, Mg, Ca, Fe, Cu, Se and Cr for human consumption. Regarding contaminants, As, Cd and Pb concentrations in dried sea cucumbers were in the ranges of 1.1-6.1, 0.03-0.06 and 0.11-0.69 mg kg(-1), respectively. Moreover, Hg values of 11 sea cucumbers were below the detection limit (0.01 mg kg(-1)).

  11. On the enrichment of low-abundant isotopes of light chemical elements by gas centrifuges

    International Nuclear Information System (INIS)

    Borisevich, V.D.; Morozov, O.E.; Zaozerskiy, Yu.P.; Shmelev, G.M.; Shipilov, Yu.D.

    2000-01-01

    A brief review of the main areas for the application of the isotopes 15 N and 13 C is made. Separation of the nitrogen isotopes in a single gas centrifuge in the form of pure nitrogen, ammonia, and trifluoride of nitrogen as well as the carbon isotopes in the form of carbon dioxide has been studied by means of numerical simulation. The parameters of the centrifugal machine investigated were close to the parameters of the Iguassu machine. The dependence of the efficiency criterion versus the basic parameters of the separation process has been explored in the computational experiments. Comparisons of the calculated results with the experimental data have shown good agreement. The results obtained have demonstrated the possibility of using gas centrifuge technology to enrich successfully the low-abundant isotopes of light chemical elements

  12. Effects of cleaning methods upon preservation of stable isotopes and trace elements in shells of Cyprideis torosa (Crustacea, Ostracoda): Implications for palaeoenvironmental reconstruction

    Science.gov (United States)

    Roberts, L. R.; Holmes, J. A.; Leng, M. J.; Sloane, H. J.; Horne, D. J.

    2018-06-01

    The trace element (Sr/Ca and Mg/Ca) and stable isotope (δ18O and δ13C) geochemistry of fossil ostracod valves provide valuable information, particularly in lacustrine settings, on palaeo-water composition and palaeotemperature. The removal of sedimentary and organic contamination prior to geochemical analysis is essential to avoid bias of the results. Previous stable isotope and trace element work on ostracod shells has, however, employed different treatments for the removal of contamination beyond simple 'manual' cleaning using a paint brush and methanol under a low-power binocular microscope. For isotopic work pre-treatments include chemical oxidation, vacuum roasting and plasma ashing, and for trace element work sonication, chemical oxidation and reductive cleaning. The impact of different treatments on the geochemical composition of the valve calcite has not been evaluated in full, and a universal protocol has not been established. Here, a systematic investigation of the cleaning methods is undertaken using specimens of the ubiquitous euryhaline species, Cyprideis torosa. Cleaning methods are evaluated by undertaking paired analyses on a single carapace (comprising two valves); in modern ostracods, whose valves are assumed to be unaltered, the two valves should have identical geochemical and isotopic composition. Hence, when one valve is subjected to the chosen treatment and the other to simple manual cleaning any difference in composition can confidently be assigned to the treatment method. We show that certain cleaning methods have the potential to cause alteration to the geochemical signal, particularly Mg/Ca and δ18O, and hence have implications for palaeoenvironmental reconstructions. For trace-element determinations we recommend cleaning by sonication and for stable isotope analysis, oxidation by hydrogen peroxide. These methods remove contamination, yet do not significantly alter the geochemical signal.

  13. Experimental study on effect of flux composition on element transfer ...

    Indian Academy of Sciences (India)

    BRIJPAL SINGH

    2018-03-10

    Mar 10, 2018 ... 3 Division of Manufacturing Processes and Automation Engineering, Netaji Subhas Institute of ... Submerged arc welding; basicity index; element transfer; slag metal reactions; oxidizing power of ... flux composition, wire and base plate composition. ..... increase in BI of the flux with increasing NiO additive. If.

  14. High burn-up plutonium isotopic compositions recommended for use in shielding analysis

    International Nuclear Information System (INIS)

    Zimmerman, M.G.

    1977-06-01

    Isotopic compositions for plutonium generated and recycled in LWR's were estimated for use in shielding calculations. The values were obtained by averaging isotopic values from many sources in the literature. These isotopic values should provide the basis for a reasonable prediction of exposure rates from the range of LWR fuel expected in the future. The isotopic compositions given are meant to be used for shielding calculations, and the values are not necessarily applicable to other forms of analysis, such as inventory assessment or criticality safety. 11 tables, 2 figs

  15. Isotopic composition of strontium in three basalt-andesite centers along the Lesser Antilles arc

    Science.gov (United States)

    Hedge, C.E.; Lewis, J.F.

    1971-01-01

    Si87/Sr86 ratios have been determined for lavas and py lastic rocks from three basalt-andesite centers along the Lesser Antilles arc-Mt. Misery on the island of St. Kitts, Soufriere on the island of St. Vincent, and Carriacou, an island of The Grenadines. The average Si87/Sr86 content of these rocks is 0.7038 for Mt. Misery, 0.7041 for Soufriere, and 0.7053 for Carriacou. All the Sr87/Sr86 values from each center are the same within analytical uncertainty (??0.0002). The constancy of strontium isotopic data within each center supports the hypothesis that basalts and andesites for each specific center investigated are generated from the same source - in agreement with petrographic and major- and minor-element data. Strontium isotopic compositions and elemental concentrations, particularly of strontium and nickel, indicate that this source was mantle peridotite and that the relationship between the respective basalts and andesites is probably fractional crystallization. ?? 1971 Springer-Verlag.

  16. Americium-241: the most useful isotope of the actinide elements

    International Nuclear Information System (INIS)

    Navratil, J.D.

    1984-01-01

    Used extensively in nuclear gauges and in many other areas, this man-made element (Atomic Number 95) was first isolated in weighable amounts during World War II. Americium is now a very useful by-product of the nuclear industry and is produced in kilogram amounts by appropriate recovery, separation and purification processes. A review will be presented of its discovery, nuclear and chemical properties, and uses, with emphasis on its production process and separations chemistry

  17. Impact of metabolism and growth phase on the hydrogen isotopic composition of microbial fatty acids

    Science.gov (United States)

    Heinzelmann, Sandra M.; Villanueva, Laura; Sinke-Schoen, Danielle; Sinninghe Damsté, Jaap S.; Schouten, Stefan; van der Meer, Marcel T. J.

    2015-01-01

    Microorganisms are involved in all elemental cycles and therefore it is important to study their metabolism in the natural environment. A recent technique to investigate this is the hydrogen isotopic composition of microbial fatty acids, i.e., heterotrophic microorganisms produce fatty acids enriched in deuterium (D) while photoautotrophic and chemoautotrophic microorganisms produce fatty acids depleted in D compared to the water in the culture medium (growth water). However, the impact of factors other than metabolism have not been investigated. Here, we evaluate the impact of growth phase compared to metabolism on the hydrogen isotopic composition of fatty acids of different environmentally relevant microorganisms with heterotrophic, photoautotrophic and chemoautotrophic metabolisms. Fatty acids produced by heterotrophs are enriched in D compared to growth water with εlipid/water between 82 and 359‰ when grown on glucose or acetate, respectively. Photoautotrophs (εlipid/water between −149 and −264‰) and chemoautotrophs (εlipid/water between −217 and −275‰) produce fatty acids depleted in D. Fatty acids become, in general, enriched by between 4 and 46‰ with growth phase which is minor compared to the influence of metabolisms. Therefore, the D/H ratio of fatty acids is a promising tool to investigate community metabolisms in nature. PMID:26005437

  18. Nutritional assessment by isotope dilution analysis of body composition

    International Nuclear Information System (INIS)

    Szeluga, D.J.; Stuart, R.K.; Utermohlen, V.; Santos, G.W.

    1984-01-01

    The three components of body mass, body cell mass (BCM), extracellular fluid (ECF), and fat + extracellular solids (ECS: bone, tendon, etc) can be quantified using established isotope dilution techniques. With these techniques, total body water (TBW) and ECF are measured using 3H 2 O and 82 Bromine, respectively, as tracers. BCM is calculated from intracellular fluid (ICF) where ICF . TBW - ECF. Fat + ECS is estimated as: body weight - (BCM + ECF). TBW and ECF can be determined by either of two calculation methods, one requiring several timed plasma samples (extrapolation method) and one requiring a single plasma sample and a 4-h urine collection (urine-corrected method). The comparability of the two calculation methods was evaluated in 20 studies in 12 bone marrow transplant recipients. We found that for determination of TBW and ECF there was a very strong linear relationship (r2 greater than 0.98) between the calculation methods. Further comparisons (by t test, 2-sided) indicated that for the determination of ECF, the methods were not significantly (p greater than 0.90) different; however, TBW determined by the urine-corrected method was slightly (0.1 to 6%), but significantly (p less than 0.01) greater than that determined by the extrapolation method. Therefore, relative to the extrapolation method, the urine-corrected method ''over-estimates'' BCM and ''under-estimates'' fat + ECS since determination of these compartment sizes depends on measurement of TBW. We currently use serial isotope dilution studies to monitor the body composition changes of patients receiving therapeutic nutritional support

  19. Chemical and boron isotopic composition of tourmaline from the Mariinsky emerald deposit, Central Urals, Russia

    Science.gov (United States)

    Baksheev, Ivan A.; Trumbull, Robert B.; Popov, Mikhail P.; Erokhin, Yuri V.; Kudryavtseva, Olesya E.; Yapaskurt, Vasily O.; Khiller, Vera V.; Vovna, Galina M.; Kiselev, Vladimir I.

    2018-04-01

    Tourmaline is abundant at the Mariinsky schist-hosted emerald deposit in the Central Urals, Russia, both in emerald-bearing phlogopite veins (type 1) and later, emerald-free pockets, lenses, and veinlets cutting the phlogopite veins (type 2). The Ca content in tourmaline is influenced by the host rocks (ultramafic and mafic rocks), associated minerals, and minerals crystallized before tourmaline (amphibole, fluorite, margarite). The Na concentration in tourmaline depends on the presence or absence of paragonite, and the association with micas also strongly influences the contents of Li, Zn, Ni, and Co in tourmaline. Type 1 tourmalines associated with phlogopite are relatively depleted in these elements, whereas type 2 tourmalines associated with margarite or paragonite are enriched. Some differences in isomorphic substitutions along with the trace element composition (Zn, V, Sr, Co, REE) may have value in exploration of emerald-bearing and emerald-free veins in schist-hosted emerald deposits. The δ11B values in tourmaline of all types fall in a narrow total range from -11.3 to -8.4‰. These values, combined with a mineralization temperature of 420-360 °C, yield an estimated δ11B fluid composition of -7.4 to -6.8‰ suggesting a mixed source of boron, likely dominated from the granitic rocks surrounding the emerald belt. The narrow range of B-isotope compositions in tourmaline from throughout the Mariinsky deposit suggests a well-mixed hydrothermal system.

  20. Changing Ideas about the Periodic Table of Elements and Students' Alternative Concepts of Isotopes and Allotropes.

    Science.gov (United States)

    Schmidt, Hans-Jurgen; Baumgartner, Tim; Eybe, Holger

    2003-01-01

    Investigates secondary school students' concepts of isotopes and allotropes and how the concepts are linked to the Periodic Table of Elements (PTE). Questions senior high school students with multiple choice items and interviews. Shows that students actively tried to make sense of what they had experienced. (KHR)

  1. Qualitative PIXE analysis of mineral elements in some dental composites

    International Nuclear Information System (INIS)

    Preoteasa, E.A.; Iordan, Andreea; Harangus, Livia; Ciortea, C.; Gugiu, M.; Moldovan, Maria

    2002-01-01

    Dental composites, made by particles of glass, ceramics and quartz embedded in an organic polymer, develop at a high rate. However, commercial composites are expensive and recently the 'Restacril' biomaterials company became prepared to offer a low-cost alternative. The durability of dental fillings depends not only on biomaterial's gross chemical composition, but also on impurities. These may influence the chemical, mechanical and surface properties of the inorganic particles and modify the composites' clinical behavior. Thus elemental analysis is necessary to improve the biomaterials' quality. Nuclear and atomic methods allow sensitive multielement detection, and we previously analyzed some commercial composites by particle-induced X-ray emission (PIXE). Here we applied PIXE in the qualitative analysis of six new Romanian biomaterials, aiming to compare their nominal and detected composition and paying attention to the impurities. The PIXE measurements were performed with 3 MeV protons at the 8.5 MV NIPNE-HH tandem accelerator, using a hyper pure Ge detector, normal to the beam and connected to a multichannel analyzer and to a computer. Solid samples of composites with a flat surface were fixed at 45 angle, absorber foil of Al 30 mm thick was used, and integration of beam current was done. In all composites PIXE detected mineral elements with Z > 19 down to trace levels. All major nominal elements with Z > 20 - Ca, Sr, Zr, Ba, and Yb - were detected by PIXE. In addition, many minor and trace elements absent from the nominal formulations were seen, including K, Ti, Mn, Fe, Ni, Cu, Zn, Ga, Ag, Cd, Hf, and As/Pb. Such impurities may come from rough materials and preparative technologies. The impurities in Romanian composites are comparable to those in some commercial biomaterials but higher than in other ones. Thus PIXE analysis of mineral elements in Romanian composites, even qualitative, appears useful for quality control and improvement. (authors)

  2. Modelling and interpreting the isotopic composition of water vapour in convective updrafts

    Directory of Open Access Journals (Sweden)

    M. Bolot

    2013-08-01

    Full Text Available The isotopic compositions of water vapour and its condensates have long been used as tracers of the global hydrological cycle, but may also be useful for understanding processes within individual convective clouds. We review here the representation of processes that alter water isotopic compositions during processing of air in convective updrafts and present a unified model for water vapour isotopic evolution within undiluted deep convective cores, with a special focus on the out-of-equilibrium conditions of mixed-phase zones where metastable liquid water and ice coexist. We use our model to show that a combination of water isotopologue measurements can constrain critical convective parameters, including degree of supersaturation, supercooled water content and glaciation temperature. Important isotopic processes in updrafts include kinetic effects that are a consequence of diffusive growth or decay of cloud particles within a supersaturated or subsaturated environment; isotopic re-equilibration between vapour and supercooled droplets, which buffers isotopic distillation; and differing mechanisms of glaciation (droplet freezing vs. the Wegener–Bergeron–Findeisen process. As all of these processes are related to updraft strength, particle size distribution and the retention of supercooled water, isotopic measurements can serve as a probe of in-cloud conditions of importance to convective processes. We study the sensitivity of the profile of water vapour isotopic composition to differing model assumptions and show how measurements of isotopic composition at cloud base and cloud top alone may be sufficient to retrieve key cloud parameters.

  3. Modelling and interpreting the isotopic composition of water vapour in convective updrafts

    Science.gov (United States)

    Bolot, M.; Legras, B.; Moyer, E. J.

    2013-08-01

    The isotopic compositions of water vapour and its condensates have long been used as tracers of the global hydrological cycle, but may also be useful for understanding processes within individual convective clouds. We review here the representation of processes that alter water isotopic compositions during processing of air in convective updrafts and present a unified model for water vapour isotopic evolution within undiluted deep convective cores, with a special focus on the out-of-equilibrium conditions of mixed-phase zones where metastable liquid water and ice coexist. We use our model to show that a combination of water isotopologue measurements can constrain critical convective parameters, including degree of supersaturation, supercooled water content and glaciation temperature. Important isotopic processes in updrafts include kinetic effects that are a consequence of diffusive growth or decay of cloud particles within a supersaturated or subsaturated environment; isotopic re-equilibration between vapour and supercooled droplets, which buffers isotopic distillation; and differing mechanisms of glaciation (droplet freezing vs. the Wegener-Bergeron-Findeisen process). As all of these processes are related to updraft strength, particle size distribution and the retention of supercooled water, isotopic measurements can serve as a probe of in-cloud conditions of importance to convective processes. We study the sensitivity of the profile of water vapour isotopic composition to differing model assumptions and show how measurements of isotopic composition at cloud base and cloud top alone may be sufficient to retrieve key cloud parameters.

  4. Modelling and intepreting the isotopic composition of water vapour in convective updrafts

    Science.gov (United States)

    Bolot, M.; Legras, B.; Moyer, E. J.

    2012-08-01

    The isotopic compositions of water vapour and its condensates have long been used as tracers of the global hydrological cycle, but may also be useful for understanding processes within individual convective clouds. We review here the representation of processes that alter water isotopic compositions during processing of air in convective updrafts and present a unified model for water vapour isotopic evolution within undiluted deep convective cores, with a special focus on the out-of-equilibrium conditions of mixed phase zones where metastable liquid water and ice coexist. We use our model to show that a combination of water isotopologue measurements can constrain critical convective parameters including degree of supersaturation, supercooled water content and glaciation temperature. Important isotopic processes in updrafts include kinetic effects that are a consequence of diffusive growth or decay of cloud particles within a supersaturated or subsaturated environment; isotopic re-equilibration between vapour and supercooled droplets, which buffers isotopic distillation; and differing mechanisms of glaciation (droplet freezing vs. the Wegener-Bergeron-Findeisen process). As all of these processes are related to updraft strength, droplet size distribution and the retention of supercooled water, isotopic measurements can serve as a probe of in-cloud conditions of importance to convective processes. We study the sensitivity of the profile of water vapour isotopic composition to differing model assumptions and show how measurements of isotopic composition at cloud base and cloud top alone may be sufficient to retrieve key cloud parameters.

  5. Elemental composition of game meat from Austria.

    Science.gov (United States)

    Ertl, Kathrin; Kitzer, Roland; Goessler, Walter

    2016-06-01

    Concentrations of 26 elements (B, Na, Mg, P, S, K, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Rb, Sr, Mo, Cd, Sb, Ba, Hg, Pb, U) in wild game meat from Austria were analysed using an inductively coupled plasma mass spectrometer. All investigated animals were culled during the hunting season 2012/2013, including 10 chamois (Rupicapra rupicapra), 9 hare (Lepus europaeus), 10 pheasant (Phasianus colchicus), 10 red deer (Cervus elaphus), 12 roe deer (Capreolus capreolus) and 10 wild boar (Sus scrofa). In 19 out of 61 meat samples lead concentrations were higher than 0.1 mg/kg, the maximum limit in meat as set by the European Commission (Regulation EC No 1881/2006), which is most likely caused by ammunition residues. Especially, pellet shot animals and chamois show a high risk for lead contamination. Despite ammunition residues all investigated muscle samples show no further health risk with respect to metal contamination.

  6. Using lead isotopes and trace element records from two contrasting Lake Tanganyika sediment cores to assess watershed – Lake exchange

    Science.gov (United States)

    Odigie, Kingsley; Cohen, A.D.; Swarzenski, Peter W.; Flegal, R

    2014-01-01

    Lead isotopic and trace element records of two contrasting sediment cores were examined to reconstruct historic, industrial contaminant inputs to Lake Tanganyika, Africa. Observed fluxes of Co, Cu, Mn, Ni, Pb, and Zn in age-dated sediments collected from the lake varied both spatially and temporally over the past two to four centuries. The fluxes of trace elements were lower (up to 10-fold) at a mid-lake site (MC1) than at a nearshore site (LT-98-58), which is directly downstream from the Kahama and Nyasanga River watersheds and adjacent to the relatively pristine Gombe Stream National Park. Trace element fluxes at that nearshore site did not measurably change over the last two centuries (1815–1998), while the distal, mid-lake site exhibited substantial changes in the fluxes of trace elements – likely caused by changes in land use – over that period. For example, the flux of Pb increased by ∼300% from 1871 to 1991. That apparent accelerated weathering and detrital mobilization of lithogenic trace elements was further evidenced by (i) positive correlations (r = 0.77–0.99, p factors (EF operations within the lake’s watershed over the past century. The data also indicate that the mid-lake site is a much more sensitive and useful recorder of environmental changes than the nearshore site. Furthermore, the lead isotopic compositions of sediment at the sites differed spatially, indicating that the Pb (and other trace elements by association) originated from different natural sources at the two locations.

  7. Controls on the stable isotope compositions of travertine from hyperalkaline springs in Oman: Insights from clumped isotope measurements

    Science.gov (United States)

    Falk, E. S.; Guo, W.; Paukert, A. N.; Matter, J. M.; Mervine, E. M.; Kelemen, P. B.

    2016-11-01

    Carbonate formation at hyperalkaline springs is typical of serpentinization in peridotite massifs worldwide. These travertines have long been known to exhibit large variations in their carbon and oxygen isotope compositions, extending from apparent equilibrium values to highly depleted values. However, the exact causes of these variations are not well constrained. We analyzed a suite of well-characterized fresh carbonate precipitates and travertines associated with hyperalkaline springs in the peridotite section of the Samail ophiolite, Sultanate of Oman, and found their clumped isotope compositions vary systematically with formation environments. Based on these findings, we identified four main processes controlling the stable isotope compositions of these carbonates. These include hydroxylation of CO2, partial isotope equilibration of dissolved inorganic carbon, mixing between isotopically distinct carbonate end-members, and post-depositional recrystallization. Most notably, in fresh crystalline films on the surface of hyperalkaline springs and in some fresh carbonate precipitates from the bottom of hyperalkaline pools, we observed large enrichments in Δ47 (up to ∼0.2‰ above expected equilibrium values) which accompany depletions in δ18O and δ13C, yielding about 0.01‰ increase in Δ47 and 1.1‰ decrease in δ13C for every 1‰ decrease in δ18O, relative to expected equilibrium values. This disequilibrium trend, also reflected in preserved travertines ranging in age from modern to ∼40,000 years old, is interpreted to arise mainly from the isotope effects associated with the hydroxylation of CO2 in high-pH fluids and agrees with our first-order theoretical estimation. In addition, in some fresh carbonate precipitates from the bottom of hyperalkaline pools and in subsamples of one preserved travertine terrace, we observed additional enrichments in Δ47 at intermediate δ13C and δ18O, consistent with mixing between isotopically distinct carbonate end

  8. Boron isotopic compositions in growing corals from the South China Sea

    Science.gov (United States)

    Xiao, Jun; Xiao, Yingkai; Jin, Zhangdong; Liu, Congqiang; He, Maoyong

    2013-01-01

    In order to determine incorporation of boron species, boron isotopic fractionation, and influence of trace elements on isotopic compositions of boron in corals (δ11Bcoral), concentrations of Mg, Sr, Na, B and δ11Bcoral in growing corals from the South China Sea were measured. Relative to seawater, Sr enriched while Mg depleted in corals in the South China Sea. Although the δ11Bcoral values were different from various species and were not closely correlated with the element concentrations in corals in the South China Sea, Mg(OH)2 existed in corals can result in high δ11Bcoral. Thus, it is necessary to examine the existence of Mg(OH)2 and to choose the same species when δ11Bcoral is used in the δ11B-pH proxy. Based on the measured δ11B values of corals and coexisting seawater as well as the seawater pH in the South China Sea, a new isotopic fractionation factor a4-3 between B(OH)4- and B(OH)3 was determined to be 0.979. Besides B(OH)4- into corals, our results showed that B(OH)3 may also be incorporated into corals with variable proportions. The incorporation of B(OH)3 into corals may challenge the hypothesis of δ11Bcoral = δ11B4, resulting in increasing uncertainty to the calculated seawater pH values to the δ11B-pH proxy. We suggested that a best-fit empirical equation between δ11B of bio-carbonates and seawater pH needs to be established by the precipitation experiments of inorganic carbonates or culture experiments of corals or foraminifera.

  9. Elements and isotopic composition of organic carbon and nitrogen

    African Journals Online (AJOL)

    conditions or high contribution of C3 high land plant materials in response to increase in forest ... smell of hydrogen sulfide detected in water samples collected at approximately 20 m, suggest that ... used δ18O and δ13C record in corals off ... experienced high temperature in 900 AD and ... Furthermore, historical records.

  10. Elemental and isotopic compositions of organic carbon and nitrogen ...

    African Journals Online (AJOL)

    The general downcore trend can be attributed to systematic changes in relative proportion between C3 and C4 types of organic matter (OM), resulting from climatic changes or nutrient changes and shift between algae and higher plants. The lower most section containing the most depleted values can be attributed either to ...

  11. Morphology, molecular structure, and stable carbon isotopic composition of black carbon (BC) in urban topsoils.

    Science.gov (United States)

    Zong, Yutong; Xiao, Qing; Lu, Shenggao

    2018-02-01

    Urban soils contain significant amounts of black carbon (BC) from biomass and fossil fuel combustion and regard to be a pool of BC. BC in urban soils has multiple effects on environmental processes in urban system, such as global climate change, air quality, and public health. Urban topsoil samples (0-10 cm) were collected from Anshan, Liaoning Province, northeast China, which is one of the most important old steel industrial bases in China. The BC in urban topsoils was extracted using the density method. Their chemical composition, morphology, molecular structure, and stable carbon isotopic composition were examined using elemental analysis, scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and stable carbon isotope (δ 13 C). Elemental analysis shows that carbon content in the BC of studied soils ranged from 64.5 to 78.4%, with the average more than 70%. The O/C atomic ratio of BC is on average 0.18. The BC particle displays different morphology, including porous spherical, irregular porous fragmentary, and blocky shapes. The porous spherical BC particles has atomic molar O/C ratio determined by SEM-EDS ranging from 0.04 to 0.37. XRD indicates that BC exists in mainly combining with mineral phases hematite (Fe 2 O 3 ), kaolinite (Al 2 Si 2 O 5 (OH) 4 ), quartz (SiO 2 ), and calcite (CaCO 3 ). The FTIR spectra of BC particles show major bands at approximately 3400 cm -1 (O-H), 2920 cm -1 (C = H), 1600 cm -1 (C = C), 1230 cm -1 (C = O), and 1070 cm -1 (C = O). The stable carbon isotope (δ 13 C) of BC ranges from -24.48 to -23.18‰ with the average of -23.79 ± 0.39‰. The concentration of BC in the industrial area is significantly (p fuel combustion. Results indicated that a combination of atomic O/C ratio, porous structure, and stable carbon isotopic (δ 13 C) of BC could reflect effectively the origin of BC

  12. Use of environmental isotope techniques in studying surface and groundwaters in the Damascus basin (Al-Ghotta): A case study of geochemical modeling of elements and pollutants transport

    International Nuclear Information System (INIS)

    Kattan, Z.

    2004-09-01

    This work discuses in details the hydrochemical and isotopic characteristics of surface and groundwaters in the Damascus Ghotta basin. In addition, it deals with the chemical and isotopic compositions of rainfall of some surrounding stations (Damascus, Bloudan, Arneh, Al-Kounietra, Izraa, Al-Souweida, Homs and Tartous). The objective of this research was to make new assessment of the available water resources in this basin, together with conducting essays to model geochemically the elements and pollutants transport in the groundwater, by the use of PHREEQM code.(author)

  13. First measurements on the core and edge isotope composition using the JET isotope separator neutral particle analyser

    International Nuclear Information System (INIS)

    Bettella, D; Murari, A; Stamp, M; Testa, D

    2003-01-01

    Direct measurements of tokamak plasmas isotope composition are in general quite difficult and have therefore been very seldom performed. On the other hand, the importance of this measurement is going to increase, as future experiments will be progressively focused on plasmas approaching reactor conditions. In this paper, we report for the first time encouraging experimental evidence supporting a new method to determine the radial profile of the density ratio n H /(n H + n D ), based on neutral particle analyser (NPA) measurements. The measurements have been performed in JET with the ISotope SEParator (ISEP), a NPA device specifically developed to measure the energy spectra of the three hydrogen isotopes with very high accuracy and low cross-talk. The data presented here have been collected in two different experimental conditions. In the first case, the density ratio has been kept constant during the discharge. The isotope ratio derived from the ISEP has been compared with the results of visible spectroscopy at the edge and with the isotope composition derived from an Alfven eigenmodes active diagnostic (AEAD) system at about half the minor radius for the discharges reported in this paper. A preliminary evaluation of the additional heating effects on the measurements has also been carried out. In the second set of experiments, the isotope composition of deuterium plasmas has been abruptly changed with suitable short blips of hydrogen, in order to assess the capability of the method to study the transport of the hydrogen isotope species. Future developments of the methodology and its applications to the evaluation of hydrogen transport coefficients are also briefly discussed. The results obtained so far motivate further development of the technique, which constitutes one of the few candidate diagnostic approaches viable for ITER

  14. Composition of bracken: some major- and trace-element constituents

    Energy Technology Data Exchange (ETDEWEB)

    Hunter, J G

    1953-01-01

    Periodic samples of bracken taken during the growing season have shown that the concentration of major elements (except calcium and sodium) decreases with age in fronds, and remains relatively constant in rhizomes, whereas trace-element concentration varies widely. Soil type has little effect on the mineral composition of fronds. Examination of three rhizome types revealed no wide differences in the content of major elements; pinnules generally contained higher concentrations of major and trace elements than fronds. Comparison of results with those published elsewhere for moorland plants grown under similar conditions indicates that bracken contains more potassium and less molybdenum.

  15. Effect of Wood Aging on Wine Mineral Composition and 87Sr/86Sr Isotopic Ratio.

    Science.gov (United States)

    Kaya, Ayse D; Bruno de Sousa, Raúl; Curvelo-Garcia, António S; Ricardo-da-Silva, Jorge M; Catarino, Sofia

    2017-06-14

    The evolution of mineral composition and wine strontium isotopic ratio 87 Sr/ 86 Sr (Sr IR) during wood aging were investigated. A red wine was aged in stainless steel tanks with French oak staves (Quercus sessiliflora Salisb.), with three industrial scale replicates. Sampling was carried out after 30, 60, and 90 days of aging, and the wines were evaluated in terms of general analysis, phenolic composition, total polysaccharides, multielement composition, and Sr IR. Li, Be, Mg, Al, Sc, Ti, V, Mn, Co, Ni, Cu, Zn, Ga, Ge, As, Rb, Sr, Y, Zr, Mo, Sb, Cs, Ba, Pr, Nd, Sm, Eu, Dy, Ho, Er, Yb, Lu, Tl, and Pb elements and 87 Sr/ 86 Sr were determined by quadrupole inductively coupled plasma mass spectrometry (Q-ICP-MS) and Na, K, Ca, and Fe by flame atomic absorption spectrometry (FAAS). Two-way ANOVA was applied to assess wood aging and time effect on Sr IR and mineral composition. Wood aging resulted in significantly higher concentrations of Mg, V, Co, Ni, and Sr. At the end of the aging period, wine exhibited statistically identical Sr IR compared to control. Study suggests that wood aging does not affect 87 Sr/ 86 Sr, not precluding the use of this parameter for wine traceability purposes.

  16. Elemental and isotope behavior of macromolecular organic matter from CM chondrites during hydrous pyrolysis

    Science.gov (United States)

    Oba, Y.; Naraoka, H.

    2009-08-01

    A new insight into carbon and hydrogen isotope variations of insoluble organic matter (IOM) is provided from seven CM chondrites, including Murchison and six Antarctic meteorites (Y-791198, Y-793321, A-881280, A-881334, A-881458 and B-7904) as well as Murchison IOM residues after hydrous pyrolysis at 270-330 °C for 72 h. Isotopic compositions of bulk carbon (δ13Cbulk) and hydrogen (δD) of the seven IOMs vary widely, ranging from -15.1 to -7.6‰ and +133 to +986‰, respectively. Intramolecular carboxyl carbon (δ13CCOOH) is more enriched in 13C by 7.5 -11‰ than bulk carbon. After hydrous pyrolysis of Murchison IOM at 330 °C, H/C ratio, δ13Cbulk, δ13CCOOH, and δD values decrease by up to 0.31, 3.5‰, 5.5‰, and 961‰, respectively. The O/C ratio increases from 0.22 to 0.46 at 270 °C and to 0.25 at 300 °C, and decreases to 0.10 at 330 °C. δ13Cbulk- δD cross plot of Murchison IOM and its pyrolysis residues shows an isotopic sequence. Of the six Antarctic IOMs, A-881280, A-881458, Y-791198 and B-7904 lie on or near the isotopic sequence depending on the degree of hydrous and/or thermal alteration, while A-881334 and Y-793321 consist of another distinct isotope group. A δ13Cbulk-δ13CCOOH cross-plot of IOMs, including Murchison pyrolysis residues, has a positive correlation between them, implying that the oxidation process to produce carboxyls is similar among all IOMs. These isotope distributions reflect various degree of alteration on the meteorite parent bodies and/or difference in original isotopic compositions before the parent body processes.

  17. Near Surface CO2 Triple Oxygen Isotope Composition

    Directory of Open Access Journals (Sweden)

    Sasadhar Mahata

    2016-02-01

    Full Text Available The isotopic composition of carbon dioxide in the atmosphere is a powerful tool for constraining its sources and sinks. In particular, the 17O oxygen anomaly [Δ17O = 1000 × ln(1 + δ17O/1000 - 0.516 × 1000 × ln(1 + δ18O/1000], with a value > 0.5‰ produced in the middle atmosphere, provides an ideal tool for probing the exchange of carbon dioxide between the biosphere/hydrosphere and atmosphere. The biosphere/hydrosphere and anthropogenic emissions give values ≤ 0.3‰. Therefore, any anomaly in near surface CO2 would reflect the balance between stratospheric input and exchange with the aforementioned surface sources. We have analyzed Δ17O values of CO2 separated from air samples collected in Taipei, Taiwan, located in the western Pacific region. The obtained mean anomaly is 0.42 ± 0.14‰ (1-σ standard deviation, in good agreement with model prediction and a published decadal record. Apart from typically used δ13C and δ18O values, the Δ17O value could provide an additional tracer for constraining the carbon cycle.

  18. Nucleosynthesis in Wolf-Rayet stars and galactic cosmic-ray isotopic composition

    International Nuclear Information System (INIS)

    Prantzos, N.

    1984-01-01

    An explanation of the isotopic composition of galactic cosmic rays could provide some clues to the mystery of their origin. It seems now that the strong stellar winds of Wolf-Rayet stars could account for most of the isotopic anomalies that have been observed in cosmic rays. Some results are presented, obtained by detailed nucleosynthesis computations. 25 references

  19. Effects of climatic seasonality on the isotopic composition of evaporating soil waters

    Directory of Open Access Journals (Sweden)

    P. Benettin

    2018-05-01

    Full Text Available Stable water isotopes are widely used in ecohydrology to trace the transport, storage, and mixing of water on its journey through landscapes and ecosystems. Evaporation leaves a characteristic signature on the isotopic composition of the water that is left behind, such that in dual-isotope space, evaporated waters plot below the local meteoric water line (LMWL that characterizes precipitation. Soil and xylem water samples can often plot below the LMWL as well, suggesting that they have also been influenced by evaporation. These soil and xylem water samples frequently plot along linear trends in dual-isotope space. These trend lines are often termed "evaporation lines" and their intersection with the LMWL is often interpreted as the isotopic composition of the precipitation source water. Here we use numerical experiments based on established isotope fractionation theory to show that these trend lines are often by-products of the seasonality in evaporative fractionation and in the isotopic composition of precipitation. Thus, they are often not true evaporation lines, and, if interpreted as such, can yield highly biased estimates of the isotopic composition of the source water.

  20. Bulk Oxygen Isotopic Composition of Ultracarbonaceous Antarctic Micrometeorites with the NanoSIMS

    Science.gov (United States)

    Kakazu, Y.; Engrand, C.; Duprat, J.; Briani, G.; Bardin, N.; Mostefaoui, S.; Duhamel, R.; Remusat, L.

    2014-09-01

    We analyzed the carbon and oxygen isotope ratios of two UCAMMs with the NanoSIMS in order to understand the origin and formation of UCAMMs. One UCAMM has 16O-rich composition and a highly heterogeneous oxygen isotopic distribution.

  1. Isotopic composition of rainfall and runoff in a small arid basin with implications for deep percolation

    International Nuclear Information System (INIS)

    Dody, A.

    1995-08-01

    The aim of this work was to characterize the isotopic composition of potential recharge in an arid rocky watershed. Unique field observations were obtained from an arid watershed in the Negev Highlands, Israel, through utilization of the dynamic variations in the isotopic composition of rainfall and runoff. The hydrological system's inputs are rainfall and its isotopic composition. Rainfall and runoff were sampled in eight storms. High variability in the isotopic composition of rainfall was observed during any single rainstorm. The isotopic distribution in the runoff at the outlet of the basin appeared often not to be correlated to the isotopic patterns of the associated rain storm. A new mathematical model was developed to describe these physical processes. The model called A Double-Component Kinematic Wave Flow and Transport Approach, was designated to assess the dynamic isotopic distribution in arid rain storms and runoff. This model simulates the transport of rainfall into overland flow and runoff in an arid rocky watershed with uniformly distributed shallow depression storage. A numerical solution for the problem was developed, to estimate the depression storage parameters. The model also reflects the isotopic memory effect due to the depression storage between sequential rain showers. A good agreement between the observed and computed hydrograph and the change of the δ 18O values in runoff in time confirms the validity of the model. (author) 138 figs., 125 refs

  2. Soil drying effects on the carbon isotope composition of soil respiration

    Science.gov (United States)

    Stable isotopes are used widely as a tool for determining sources of carbon (C) fluxes in ecosystem C studies. Environmental factors that change over time, such as moisture, can create dynamic changes in the isotopic composition of C assimilated by plants, and offers a unique opp...

  3. Isotopic composition of rainfall and runoff in a small arid basin with implications for deep percolation

    Energy Technology Data Exchange (ETDEWEB)

    Dody, A [Ben-Gurion Univ. of the Negev, Beersheba (Israel)

    1995-08-01

    The aim of this work was to characterize the isotopic composition of potential recharge in an arid rocky watershed. Unique field observations were obtained from an arid watershed in the Negev Highlands, Israel, through utilization of the dynamic variations in the isotopic composition of rainfall and runoff. The hydrological system`s inputs are rainfall and its isotopic composition. Rainfall and runoff were sampled in eight storms. High variability in the isotopic composition of rainfall was observed during any single rainstorm. The isotopic distribution in the runoff at the outlet of the basin appeared often not to be correlated to the isotopic patterns of the associated rain storm. A new mathematical model was developed to describe these physical processes. The model called A Double-Component Kinematic Wave Flow and Transport Approach, was designated to assess the dynamic isotopic distribution in arid rain storms and runoff. This model simulates the transport of rainfall into overland flow and runoff in an arid rocky watershed with uniformly distributed shallow depression storage. A numerical solution for the problem was developed, to estimate the depression storage parameters. The model also reflects the isotopic memory effect due to the depression storage between sequential rain showers. A good agreement between the observed and computed hydrograph and the change of the {delta}{sup 18O} values in runoff in time confirms the validity of the model. (author) 138 figs., 125 refs.

  4. Re-Os isotope and platinum group elements of a FOcal ZOne mantle source, Louisville Seamounts Chain, Pacific ocean

    Science.gov (United States)

    Tejada, Maria Luisa G.; Hanyu, Takeshi; Ishikawa, Akira; Senda, Ryoko; Suzuki, Katsuhiko; Fitton, Godfrey; Williams, Rebecca

    2015-02-01

    The Louisville Seamount Chain (LSC) is, besides the Hawaiian-Emperor Chain, one of the longest-lived hotspot traces. We report here the first Re-Os isotope and platinum group element (PGE) data for Canopus, Rigil, and Burton Guyots along the chain, which were drilled during IODP Expedition 330. The LSC basalts possess (187Os/188Os)i = 0.1245-0.1314 that are remarkably homogeneous and do not vary with age. A Re-Os isochron age of 64.9 ± 3.2 Ma was obtained for Burton seamount (the youngest of the three seamounts drilled), consistent with 40Ar-39Ar data. Isochron-derived initial 187Os/188Os ratio of 0.1272 ± 0.0008, together with data for olivines (0.1271-0.1275), are within the estimated primitive mantle values. This (187Os/188Os)i range is similar to those of Rarotonga (0.124-0.139) and Samoan shield (0.1276-0.1313) basalts and lower than those of Cook-Austral (0.136-0.155) and Hawaiian shield (0.1283-0.1578) basalts, suggesting little or no recycled component in the LSC mantle source. The PGE data of LSC basalts are distinct from those of oceanic lower crust. Variation in PGE patterns can be largely explained by different low degrees of melting under sulfide-saturated conditions of the same relatively fertile mantle source, consistent with their primitive mantle-like Os and primordial Ne isotope signatures. The PGE patterns and the low 187Os/188Os composition of LSC basalts contrast with those of Ontong Java Plateau (OJP) tholeiites. We conclude that the Re-Os isotope and PGE composition of LSC basalts reflect a relatively pure deep-sourced common mantle sampled by some ocean island basalts but is not discernible in the composition of OJP tholeiites.

  5. Hydrogen Isotopic Composition of Apatite in Northwest Africa 7034: A Record of the "Intermediate" H-Isotopic Reservoir in the Martian Crust?

    Science.gov (United States)

    McCubbin, F. M.; Barnes, J. J.; Santos, A. R.; Boyce, J. W.; Anand, M.; Franchi, I. A.; Agee, C. B.

    2016-01-01

    Northwest Africa (NWA) 7034 and its pairings comprise a regolith breccia with a basaltic bulk composition [1] that yields a better match than any other martian meteorite to visible-infrared reflectance spectra of the martian surface measured from orbit [2]. The composition of the fine-grained matrix within NWA 7034 bears a striking resemblance to the major element composition estimated for the martian crust, with several exceptions. The NWA 7034 matrix is depleted in Fe, Ti, and Cr and enriched in Al, Na, and P [3]. The differences in Al and Fe are the most substantial, but the Fe content of NWA 7034 matrix falls within the range reported for the southern highlands crust [6]. It was previously suggested by [4] that NWA 7034 was sourced from the southern highlands based on the ancient 4.4 Ga ages recorded in NWA 7034/7533 zircons [4, 5]. In addition, the NWA 7034 matrix material is enriched in incompatible trace elements by a factor of 1.2-1.5 [7] relative to estimates of the bulk martian crust. The La/Yb ratio of the bulk martian crust is estimated to be approximately 3 [7], and the La/Yb of the NWA 7034 matrix materials ranges from approximately 3.9 to 4.4 [3, 8], indicating a higher degree of LREE enrichment in the NWA 7034 matrix materials. This elevated La/Yb ratio and enrichment in incompatible lithophile trace elements is consistent with NWA 7034 representing a more geochemically enriched crustal terrain than is represented by the bulk martian crust, which would be expected if NWA 7034 represents the bulk crust from the southern highlands. Given the similarities between NWA 7034 and the martian crust, NWA 7034 may represent an important sample for constraining the composition of the martian crust, particularly the ancient highlands. In the present study, we seek to constrain the H isotopic composition of the martian crust using Cl-rich apatite in NWA 7034. Usui et al., [9] recently proposed that a H isotopic reservoir exists within the martian crust that has

  6. Product ion isotopologue pattern: A tool to improve the reliability of elemental composition elucidations of unknown compounds in complex matrices.

    Science.gov (United States)

    Kaufmann, A; Walker, S; Mol, G

    2016-04-15

    Elucidation of the elemental compositions of unknown compounds (e.g., in metabolomics) generally relies on the availability of accurate masses and isotopic ratios. This study focuses on the information provided by the abundance ratio within a product ion pair (monoisotopic versus the first isotopic peak) when isolating and fragmenting the first isotopic ion (first isotopic mass spectrum) of the precursor. This process relies on the capability of the quadrupole within the Q Orbitrap instrument to isolate a very narrow mass window. Selecting only the first isotopic peak (first isotopic mass spectrum) leads to the observation of a unique product ion pair. The lighter ion within such an isotopologue pair is monoisotopic, while the heavier ion contains a single carbon isotope. The observed abundance ratio is governed by the percentage of carbon atoms lost during the fragmentation and can be described by a hypergeometric distribution. The observed carbon isotopologue abundance ratio (product ion isotopologue pattern) gives reliable information regarding the percentage of carbon atoms lost in the fragmentation process. It therefore facilitates the elucidation of the involved precursor and product ions. Unlike conventional isotopic abundances, the product ion isotopologue pattern is hardly affected by isobaric interferences. Furthermore, the appearance of these pairs greatly aids in cleaning up a 'matrix-contaminated' product ion spectrum. The product ion isotopologue pattern is a valuable tool for structural elucidation. It increases confidence in results and permits structural elucidations for heavier ions. This tool is also very useful in elucidating the elemental composition of product ions. Such information is highly valued in the field of multi-residue analysis, where the accurate mass of product ions is required for the confirmation process. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

  7. Lead Isotope Compositions of Acid Residues from Olivine-Phyric Shergottite Tissint: Implications for Heterogeneous Shergottite Source Reservoirs

    Science.gov (United States)

    Moriwaki, R.; Usui, T.; Yokoyama, T.; Simon, J. I.; Jones, J. H.

    2015-01-01

    Geochemical studies of shergottites suggest that their parental magmas reflect mixtures between at least two distinct geochemical source reservoirs, producing correlations between radiogenic isotope compositions and trace element abundances. These correlations have been interpreted as indicating the presence of a reduced, incompatible element- depleted reservoir and an oxidized, incompatible- element-enriched reservoir. The former is clearly a depleted mantle source, but there is ongoing debate regarding the origin of the enriched reservoir. Two contrasting models have been proposed regarding the location and mixing process of the two geochemical source reservoirs: (1) assimilation of oxidized crust by mantle derived, reduced magmas, or (2) mixing of two distinct mantle reservoirs during melting. The former requires the ancient Martian crust to be the enriched source (crustal assimilation), whereas the latter requires isolation of a long-lived enriched mantle domain that probably originated from residual melts formed during solidification of a magma ocean (heterogeneous mantle model). This study conducts Pb isotope and trace element concentration analyses of sequential acid-leaching fractions (leachates and the final residues) from the geochemically depleted olivine-phyric shergottite Tissint. The results suggest that the Tissint magma is not isotopically uniform and sampled at least two geochemical source reservoirs, implying that either crustal assimilation or magma mixing would have played a role in the Tissint petrogenesis.

  8. Stable isotope composition of mercury forms in flue gases from a typical coal-fired power plant, Inner Mongolia, northern China

    International Nuclear Information System (INIS)

    Tang, Shunlin; Feng, Chaohui; Feng, Xinbin; Zhu, Jianming; Sun, Ruoyu; Fan, Huipeng; Wang, Lina; Li, Ruiyang; Mao, Tonghua; Zhou, Ting

    2017-01-01

    Highlights: • The first speciated Hg isotope ratios in coal combustion flue gases are presented. • Significant Hg isotope kinetic MDF was observed during Hg forms transformation. • Emitted gaseous Hg highly enriches in heavy Hg isotopes relative to feed coal. - Abstract: Mercury forms emitted from coal combustion via air pollution control devices are speculated to carry different Hg isotope signatures. Yet, their Hg isotope composition is still not reported. Here, we present the first onsite Hg isotope data for gaseous elemental Hg (GEM) and gaseous oxidized Hg (GOM) of flue gases from a typical lignite-fired power plant (CFPP). Significant mass dependent fractionation (MDF) and insignificant mass independent fractionation (MIF) are observed between feed coal and coal combustion products. As compared to feed coal (δ 202 Hg = −2.04 ± 0.25‰), bottom ash, GEM and GOM in flue gases before and after wet flue gas desulfurization system significantly enrich heavy Hg isotopes by 0.7–2.6‰ in δ 202 Hg, while fly ash, desulfurization gypsum and waste water show slight but insignificant enrichment of light Hg isotopes. GEM is significantly enriched heavy Hg isotopes compared to GOM and Hg in fly ash. Our observations verify the previous speculation on Hg isotope fractionation mechanism in CFPPs, and suggest a kinetically-controlled mass dependent Hg isotope fractionation during transformation of Hg forms in flue gases. Finally, our data are compared to Hg isotope compositions of atmospheric Hg pools, suggesting that coal combustion Hg emission is likely an important atmospheric Hg contributor.

  9. Stable isotope composition of mercury forms in flue gases from a typical coal-fired power plant, Inner Mongolia, northern China

    Energy Technology Data Exchange (ETDEWEB)

    Tang, Shunlin, E-mail: tangshunlin@hpu.edu.cn [Institute of Resources and Environment, Henan Polytechnic University, Jiaozuo, Henan Province, 454000 (China); Feng, Chaohui [Institute of Resources and Environment, Henan Polytechnic University, Jiaozuo, Henan Province, 454000 (China); Feng, Xinbin [State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang, 550002 (China); Zhu, Jianming [Institute of Resources and Environment, Henan Polytechnic University, Jiaozuo, Henan Province, 454000 (China); State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Beijing, 100086 (China); Sun, Ruoyu, E-mail: ruoyu.sun@tju.edu.cn [CAS Key Laboratory of Crust-Mantle Materials and Environment, School of Earth and Space Sciences, University of Science and Technology of China, Hefei, Anhui 230026 (China); Fan, Huipeng; Wang, Lina; Li, Ruiyang; Mao, Tonghua [Institute of Resources and Environment, Henan Polytechnic University, Jiaozuo, Henan Province, 454000 (China); Zhou, Ting [State Key Laboratory of Ore Deposit Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guiyang, 550002 (China)

    2017-04-15

    Highlights: • The first speciated Hg isotope ratios in coal combustion flue gases are presented. • Significant Hg isotope kinetic MDF was observed during Hg forms transformation. • Emitted gaseous Hg highly enriches in heavy Hg isotopes relative to feed coal. - Abstract: Mercury forms emitted from coal combustion via air pollution control devices are speculated to carry different Hg isotope signatures. Yet, their Hg isotope composition is still not reported. Here, we present the first onsite Hg isotope data for gaseous elemental Hg (GEM) and gaseous oxidized Hg (GOM) of flue gases from a typical lignite-fired power plant (CFPP). Significant mass dependent fractionation (MDF) and insignificant mass independent fractionation (MIF) are observed between feed coal and coal combustion products. As compared to feed coal (δ{sup 202}Hg = −2.04 ± 0.25‰), bottom ash, GEM and GOM in flue gases before and after wet flue gas desulfurization system significantly enrich heavy Hg isotopes by 0.7–2.6‰ in δ{sup 202}Hg, while fly ash, desulfurization gypsum and waste water show slight but insignificant enrichment of light Hg isotopes. GEM is significantly enriched heavy Hg isotopes compared to GOM and Hg in fly ash. Our observations verify the previous speculation on Hg isotope fractionation mechanism in CFPPs, and suggest a kinetically-controlled mass dependent Hg isotope fractionation during transformation of Hg forms in flue gases. Finally, our data are compared to Hg isotope compositions of atmospheric Hg pools, suggesting that coal combustion Hg emission is likely an important atmospheric Hg contributor.

  10. Usage of burnt fuel isotopic compositions from engineering codes in Monte-Carlo code calculations

    International Nuclear Information System (INIS)

    Aleshin, Sergey S.; Gorodkov, Sergey S.; Shcherenko, Anna I.

    2015-01-01

    A burn-up calculation of VVER's cores by Monte-Carlo code is complex process and requires large computational costs. This fact makes Monte-Carlo codes usage complicated for project and operating calculations. Previously prepared isotopic compositions are proposed to use for the Monte-Carlo code (MCU) calculations of different states of VVER's core with burnt fuel. Isotopic compositions are proposed to calculate by an approximation method. The approximation method is based on usage of a spectral functionality and reference isotopic compositions, that are calculated by engineering codes (TVS-M, PERMAK-A). The multiplication factors and power distributions of FA and VVER with infinite height are calculated in this work by the Monte-Carlo code MCU using earlier prepared isotopic compositions. The MCU calculation data were compared with the data which were obtained by engineering codes.

  11. Non-constant relative atomic masses due to varying isotopic abundance of polynuclidic elements and their effect on the accuracy of analytical results

    International Nuclear Information System (INIS)

    Gerstenberger, H.

    1981-01-01

    Alterations of actual relative atomic masses occur in natural samples by natural isotope ratio shifts of polynuclidic elements. Therefore, using nuclear properties for gaining a measuring signal, isotopic shifts of certain elements may lead to significant measuring errors

  12. Carbon-13 kinetic isotope effects in the decarbonylation of lactic acid of natural isotopic composition in phosphoric acid medium

    International Nuclear Information System (INIS)

    Zielinski, M.; Czarnota, G.; Papiernik-Zielinska, H.; Kasprzyk, G.; Gumolka, L.; Staedter, W.

    1993-01-01

    The 13 C kinetic isotope effect fractionation in the decarbonylation of lactic acid (LA) of natural isotopic composition by concentrated phosphoric acids (PA) and by 85% H 3 PO 4 has been studied in the temperature interval of 60-150 deg C. The values of the 13 C (1) isotope effects in the decarbonylation of lactic acid in 100% H 3 PO 4 , in pyrophosphoric acid and in more concentrated phosphoric acids are intermediate between the values calculated assuming that the C (1)- OH bond is broken in the rate-controlling step of dehydration and those calculated for rupture of the carbon-carbon bond in the transition state. In the temperature interval of 90-130 deg C the experimental 13 C fractionation factors determined in concentrated PA approach quite closely the 13 C fractionation corresponding to C (2)- C (1) bond scission. The 13 C (1) kinetic isotope effects in the decarbonylation of LA in 85% orthophosphoric acid in the temperature range of 110-150 deg C coincide with the 13 C isotope effects calculated assuming that the frequency corresponding to the C (1) -OH vibration is lost in the transition state of decarbonylation. A change of the mechanism of decarbonylation of LA in going from concentrated PA medium to 85% H 3 PO 4 has been suggested. A possible secondary 18 O and a primary 18 O kinetic isotope effect in decarbonylation of lactic acid in phosphoric acids media have been discussed, too. (author) 21 refs.; 3 tabs

  13. Isotopic composition of Pb and Th in interplinian volcanics from Somma-Vesuvius volcano, Italy

    International Nuclear Information System (INIS)

    Cortini, M.; De Vivo, B.; Somma, R.; Ayuso, R.A.; Holden, P.

    2004-01-01

    We present a detailed isotopic study of volcanic rocks emitted from Somma-Vesuvius volcano during three periods of interplinian activity: 'Protohistoric' (3550 y B.P. to 79 A.D.), 'Ancient Historic' (79 to 472 A.D.) and 'Medieval' (472 to 1631 A.D.). Pb isotopic compositions of two acid leached fractions and whole rock residues of 37 whole rock samples (determined by Somma et al., 2001) show that each of the three interplinian periods is distinguished by small, systematic, and unique uranogenic and thorogenic Pb isotopic trends. This key and novel feature is compatible with the notion that the Pb isotopic data reflect small-scale source heterogeneity operating over relatively short periods of time. From this representative group of samples, a selected set of nine whole rocks were analyzed for Th isotopes. 232 Th/ 238 U ratios in the source can be obtained independently from Pb and from Th isotopes. Those obtained from Pb isotopes represent source ratios, time-integrated over the whole age of the earth; they range from 3.9 to 4.1. 232 Th/ 238 U obtained from Th isotopes are those of the present source. They are lower, and cluster around 3.5; this difference probably indicates recent U enrichment of the present source. The behavior of Pb, as inferred by its isotopic ratios, is quite distinct from that of Sr and Nd isotopes: Pb isotope variations are not correlated to Sr or Nd isotope variations. The isotopic contrast is compatible with the idea that the isotopes were decoupled during magmatic production, evolution, and ascent through the crust. Thus, the Pb isotopes do not reflect the effects of the same processes as in the case of the Sr and Nd isotopes, or, as we also favor, they do not necessarily reflect the same source contributions into the magmas. Moreover, the Pb isotopic evolution of the interplinian rocks chiefly reflects mixing, driven by processes that are superimposed on, and independent of, other source contributions that determine the isotopic

  14. Fast XRF analysis of mineral elements in dental composites

    International Nuclear Information System (INIS)

    Preoteasa, E. A.; Constantinescu, B.; Preoteasa, E.

    2001-01-01

    Dental composites, made of particles of glass, ceramics or quartz embedded in an organic polymer matrix, extensively replaced silver amalgam in tooth fillings and enabled new applications for restorative dentistry. Long-term alteration of dental fillings together with market pressure motivates the development of composites at a high rate, largely by progress of materials forming their mineral phase. Therefore, dental composites constantly bring at the interface with enamel and dentine new elements foreign to the organism, whose biological action has not been studied. Atomic and nuclear methods for surface multielemental analysis have been used in dental research but not for composites. X-ray fluorescence (XRF) is suited for the fast microanalytical screening of the elements and of their changes at the biomaterial's surface. The potential of radioisotope-excited XRF for the analysis of dental composites has been examined. Flat disk-shaped samples of composites have been prepared and polymerized chemically or by irradiation with intense 420-500 nm light. The measurements were performed with a spectrometric chain containing a 30 mCi source of 241 Am, a Si(Li) detector, and a multichannel analyzer. The spectra were built up for 2000-6000 sec. The characteristic X lines were integrated and normalized to source lines. The following Z ≥ 20 elements were detected in the studied composites: Ba only in Charisma (Kulzer) and Pekafill (Bayer); Zr, Ba, Yb in Tetric Ceram, and Ca, Ba, Yb together with traces of possibly Ti and Fe in Ariston (both from Vivadent); Zr, Hf in Valux Plus (3M Dental); and Sr, Ba together with some trace element, seemingly Cu, in F2000 Compomer (3M Dental) and with other trace elements like Ca, Fe in Surefil (Dentsply). Among older materials, Concise (3M Dental) contained only light (Z 3 that releases F for protection of enamel and dentine. Yb, Zr, Ba, Hf improve the radiological opacity of the materials. Some elements may accompany others as

  15. Use of lead isotopic composition in sulfides for the mineral-formation geochronology

    International Nuclear Information System (INIS)

    Ordynets, G.E.

    1977-01-01

    A study of the isotopic composition of lead in pyrites and galenites of a hydrothermal uranium deposit makes it possible to determine the time of ore formation. A few types of lead ores are distinguished. Each type corresponds to a definite period of mineralization and is characterized by a specific isotopic composition. The Cimmerian age of carbonate-sulphide veins has been established, the deposit being formed over a period of 150-200 million years

  16. Improvements to SFCOMPO - a database on isotopic composition of spent nuclear fuel

    International Nuclear Information System (INIS)

    Suyama, Kenya; Nouri, Ali; Mochizuki, Hiroki; Nomura, Yasushi

    2003-01-01

    Isotopic composition is one of the most relevant data to be used in the calculation of burnup of irradiated nuclear fuel. Since autumn 2002, the Organisation for Economic Co-operation and Development/Nuclear Energy Agency (OECD/NEA) has operated a database of isotopic composition - SFCOMPO, initially developed in Japan Atomic Energy Research Institute. This paper describes the latest version of SFCOMPO and the future development plan in OECD/NEA. (author)

  17. Experimental evaporation of hyperacid brines: Effects on chemical composition and chlorine isotope fractionation

    Science.gov (United States)

    Rodríguez, Alejandro; van Bergen, Manfred J.; Eggenkamp, H. G. M.

    2018-02-01

    Hyperacid brines from active volcanic lakes are some of the chemically most complex aqueous solutions on Earth. Their compositions provide valuable insights into processes of elemental transfer from a magma body to the surface and interactions with solid rocks and the atmosphere. This paper describes changes in chemical and δ37Cl signatures observed in a 1750 h isothermal evaporation experiment on hyperacid (pH 0.1) sulphate-chloride brine water from the active lake of Kawah Ijen volcano (Indonesia). Although gypsum was the only evaporite mineral identified in the evolving brine, decreasing Si concentrations may ultimately result in amorphous silica precipitation. Geochemical simulations predict the additional formation of elemental sulphur at lower water activities (aH2O ≤ 0.65) that were not reached in the experiment. Absence of other sulphates and halides despite the high load of dissolved elements (initial TDS ca. 100 g/kg) can be attributed to increased solubility of metals, promoted by extensive formation of complexes between the variety of cations and the major anions (HSO4-, Cl-, F-) present. Chlorine deviations from a conservative behaviour point to losses of gaseous hydrogen chloride (HCl(g)) and consequently an increase in Br/Cl ratios. Chlorine isotope fractionation that accompanied the escape of HCl(g) showed a marked change in sign and magnitude in the course of progressive evaporation of the brine. The calculated factor of fractionation between HCl(g) and dissolved Cl for the initial interval (before 500 h) is positive (1000lnαHCl(g)-Cldiss. = + 1.55 ± 0.49‰to + 3.37 ± 1.11‰), indicating that, at first, the escaping HCl(g) was isotopically heavier than the dissolved Cl remaining in the brine. Conversely, fractionation shifted to the opposite direction in the subsequent interval (1000lnαHCl(g)-Cldiss. = 5.67 ± 0.17‰to - 5.64 ± 0.08‰), in agreement with values reported in literature. It is proposed that Cl isotopic fractionation in

  18. Isotopic compositions of potassium and calcium in magnetic spherulesfrom marine sediments

    International Nuclear Information System (INIS)

    Shimarura, T.; Yanagita, S.; Yamakoshi, K.; Nogami, K.; Arai, O.; Tazawa, Y.; Kobayashi, K.

    1979-01-01

    Isotopic compositions of potassium and calcium in individual magnetic spherules were determined. No significant anomaly was observed for potassium within twice the statistical error (2sigma), although for calcium isotopes enrichment of 46 Ca, 44 Ca and 42 Ca were observed in one spherule. The relative excess of 46 Ca, 44 Ca and 42 Ca in the spherule agrees with the relative yield of spallogenic calcium isotopes observed in iron meteorites. This fact indicates that the enrichment in the calcium isotopes was caused by cosmic ray irradiation of the spherule in outer space. (Auth.)

  19. Isotopic and trace element variability in altered and unaltered tuffs at Yucca Mountain, Nevada

    Science.gov (United States)

    Peterman, Z.E.; Spengler, R.W.; Singer, F.R.; Dickerson, R.P.

    1993-01-01

    Reference stratigraphic sections near Yucca Mountain, Nevada were established and sampled in outcrop areas where the volcanic rocks have been minimally altered. Isotopic and trace element analyses obtained for these reference sections are baseline data for assessing the degree and extent of element mobility attendant with past zonal alteration of the rock mass. In agreement with earlier studies, zeolitization is shown to have occurred under wholesale open-system conditions. Calcium was increased by two three times the baseline values and strontium up to twenty times. In contrast, barium displays less variability, and the high-field strength elements zirconium and titanium were the least mobile during zeolitization. The data reported here establish the usefulness of reference sections of assessing past elements mobility. The information gained will be helpful in predicting possible future element mobility induced by thermally activated fluids in the near field of a potential repository.

  20. Development of routines for simultaneous in situ chemical composition and stable Si isotope ratio analysis by femtosecond laser ablation inductively coupled plasma mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Frick, Daniel A., E-mail: dfrick@gfz-potsdam.de [GFZ German Research Centre for Geosciences, 14473 Potsdam (Germany); Schuessler, Jan A. [GFZ German Research Centre for Geosciences, 14473 Potsdam (Germany); Blanckenburg, Friedhelm von [GFZ German Research Centre for Geosciences, 14473 Potsdam (Germany); Institute of Geological Science, Freie Universität Berlin, 12249 Berlin (Germany)

    2016-09-28

    Stable metal (e.g. Li, Mg, Ca, Fe, Cu, Zn, and Mo) and metalloid (B, Si, Ge) isotope ratio systems have emerged as geochemical tracers to fingerprint distinct physicochemical reactions. These systems are relevant to many Earth Science questions. The benefit of in situ microscale analysis using laser ablation (LA) over bulk sample analysis is to use the spatial context of different phases in the solid sample to disclose the processes that govern their chemical and isotopic compositions. However, there is a lack of in situ analytical routines to obtain a samples' stable isotope ratio together with its chemical composition. Here, we evaluate two novel analytical routines for the simultaneous determination of the chemical and Si stable isotope composition (δ{sup 30}Si) on the micrometre scale in geological samples. In both routines, multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) is combined with femtosecond-LA, where stable isotope ratios are corrected for mass bias using standard-sample-bracketing with matrix-independent calibration. The first method is based on laser ablation split stream (LASS), where the laser aerosol is split and introduced simultaneously into both the MC-ICP-MS and a quadrupole ICP-MS. The second method is based on optical emission spectroscopy using direct observation of the MC-ICP-MS plasma (LA-MC-ICP-MS|OES). Both methods are evaluated using international geological reference materials. Accurate and precise Si isotope ratios were obtained with an uncertainty typically better than 0.23‰, 2SD, δ{sup 30}Si. With both methods major element concentrations (e.g., Na, Al, Si, Mg, Ca) can be simultaneously determined. However, LASS-ICP-MS is superior over LA-MC-ICP-MS|OES, which is limited by its lower sensitivity. Moreover, LASS-ICP-MS offers trace element analysis down to the μg g{sup −1}-range for more than 28 elements due to lower limits of detection, and with typical uncertainties better than 15%. For in situ

  1. Development of routines for simultaneous in situ chemical composition and stable Si isotope ratio analysis by femtosecond laser ablation inductively coupled plasma mass spectrometry

    International Nuclear Information System (INIS)

    Frick, Daniel A.; Schuessler, Jan A.; Blanckenburg, Friedhelm von

    2016-01-01

    Stable metal (e.g. Li, Mg, Ca, Fe, Cu, Zn, and Mo) and metalloid (B, Si, Ge) isotope ratio systems have emerged as geochemical tracers to fingerprint distinct physicochemical reactions. These systems are relevant to many Earth Science questions. The benefit of in situ microscale analysis using laser ablation (LA) over bulk sample analysis is to use the spatial context of different phases in the solid sample to disclose the processes that govern their chemical and isotopic compositions. However, there is a lack of in situ analytical routines to obtain a samples' stable isotope ratio together with its chemical composition. Here, we evaluate two novel analytical routines for the simultaneous determination of the chemical and Si stable isotope composition (δ 30 Si) on the micrometre scale in geological samples. In both routines, multicollector inductively coupled plasma mass spectrometry (MC-ICP-MS) is combined with femtosecond-LA, where stable isotope ratios are corrected for mass bias using standard-sample-bracketing with matrix-independent calibration. The first method is based on laser ablation split stream (LASS), where the laser aerosol is split and introduced simultaneously into both the MC-ICP-MS and a quadrupole ICP-MS. The second method is based on optical emission spectroscopy using direct observation of the MC-ICP-MS plasma (LA-MC-ICP-MS|OES). Both methods are evaluated using international geological reference materials. Accurate and precise Si isotope ratios were obtained with an uncertainty typically better than 0.23‰, 2SD, δ 30 Si. With both methods major element concentrations (e.g., Na, Al, Si, Mg, Ca) can be simultaneously determined. However, LASS-ICP-MS is superior over LA-MC-ICP-MS|OES, which is limited by its lower sensitivity. Moreover, LASS-ICP-MS offers trace element analysis down to the μg g −1 -range for more than 28 elements due to lower limits of detection, and with typical uncertainties better than 15%. For in situ

  2. Effects of trace element concentration on enzyme controlled stable isotope fractionation during aerobic biodegradation of toluene.

    Science.gov (United States)

    Mancini, Silvia A; Hirschorn, Sarah K; Elsner, Martin; Lacrampe-Couloume, Georges; Sleep, Brent E; Edwards, Elizabeth A; Lollar, Barbara Sherwood

    2006-12-15

    The effects of iron concentration on carbon and hydrogen isotopic fractionation during aerobic biodegradation of toluene by Pseudomonas putida mt-2 were investigated using a low iron medium and two different high iron media. Mean carbon enrichment factors (epsilonc) determined using a Rayleigh isotopic model were smaller in culture grown under high iron conditions (epsilonc = -1.7+/-0.1%) compared to low iron conditions (epsilonc = -2.5+/-0.3%). Mean hydrogen enrichment factors (epsilonH) were also significantly smaller for culture grown under high iron conditions (epsilonH = -77 +/-4%) versus low iron conditions (EpsilonH = -159+/-11%). A mechanistic model for enzyme kinetics was used to relate differences in the magnitude of isotopic fractionation for low iron versus high iron cultures to the efficiency of the enzymatic transformation. The increase of carbon and hydrogen enrichment factors at low iron concentrations suggests a slower enzyme-catalyzed substrate conversion step (k2) relative to the enzyme-substrate binding step (k-l) at low iron concentration. While the observed differences were subtle and, hence, do not significantly impact the ability to use stable isotope analysis in the field, these results demonstrated that resolvable differences in carbon and hydrogen isotopic fractionation were related to low and high iron conditions. This novel result highlights the need to further investigate the effects of other trace elements known to be key components of biodegradative enzymes.

  3. Identifying the origins of local atmospheric deposition in the steel industry basin of Luxembourg using the chemical and isotopic composition of the lichen Xanthoria parietina.

    Science.gov (United States)

    Hissler, Christophe; Stille, Peter; Krein, Andreas; Geagea, Majdi Lahd; Perrone, Thierry; Probst, Jean-Luc; Hoffmann, Lucien

    2008-11-01

    Trace metal atmospheric contamination was assessed in one of the oldest European industrial sites of steel production situated in the southern part of the Grand-Duchy of Luxembourg. Using elemental ratios as well as Pb, Sr, and Nd isotopic compositions as tracers, we found preliminary results concerning the trace metal enrichment and the chemical/isotopic signatures of the most important emission sources using the lichen Xanthoria parietina sampled at 15 sites along a SW-NE transect. The concentrations of these elements decreased with increasing distance from the historical and actual steel-work areas. The combination of the different tracers (major elements, Rare Earth Element ratios, Pb, Sr and Nd isotopes) enabled us to distinguish between three principal sources: the historical steel production (old tailings corresponding to blast-furnace residues), the present steel production (industrial sites with arc electric furnace units) and the regional background (baseline) components. Other anthropogenic sources including a waste incinerator and major roads had only weak impacts on lichen chemistry and isotopic ratios. The correlation between the Sr and Nd isotope ratios indicated that the Sr-Nd isotope systems represented useful tools to trace atmospheric emissions of factories using scrap metal for steel production.

  4. Isotopic composition of Danube water in the pre-delta section from the years 2009 - 2012

    Directory of Open Access Journals (Sweden)

    RANK Dieter

    2013-12-01

    Full Text Available The isotopic composition of river water in the Danube Basin is mainly governed by the isotopic composition of precipitation in the catchment area, evaporation effects play only a minor role. Short-term and long-term isotope signals from precipitation are thus transmitted through the whole catchment. The isotopic composition of Danube water in the Delta region so provides an integrated isotope signal for climatic/hydrological conditions and changes in the whole catchment. The aim of this investigation was to establish a representative isotope monitoring near the Danube Delta. The results showed that the Danube River is regarding isotope content fully mixed at the bifurcation of the Danube Delta arms. Therefore routine sampling at only one location in the pre-delta region should be sufficient to obtain a representative isotope record for the whole Danube Basin. The δ 18 O time series from November 2009 to May 2012 (sampling twice a month shows seasonal variations in the range of -9.8 ‰ ± 0.7 ‰ with a minimum in spring and a maximum in autumn. The tritium results exhibit the influence of short term contaminations due to human activities. The expected “environmental” tritium content of river water in Central Europe would be about 10 TU. During this investigation 3 H values up to 100 TU were observed in the pre-delta section. This indicates short terms releases of tritium from local sources such as nuclear power plants in the Danube river system.

  5. Metallic elements and isotope of Pb in wet precipitation in urban area, South America

    Science.gov (United States)

    Migliavacca, Daniela Montanari; Teixeira, Elba Calesso; Gervasoni, Fernanda; Conceição, Rommulo Vieira; Raya Rodriguez, Maria Teresa

    2012-04-01

    The atmosphere of urban areas has been the subject of many studies to show the atmospheric pollution in large urban centers. By quantifying wet precipitation through the analysis of metallic elements (ICP/AES) and Pb isotopes, the wet precipitation of the Metropolitan Area of the Porto Alegre (MAPA), Brazil, was characterized. The samples were collected between July 2005 and December 2007. Zn, Fe and Mn showed the highest concentration in studied sites. Sapucaia do Sul showed the highest average for Zn, due to influence by the steel plant located near the sampling site. The contribution of anthropogenic emissions from vehicular activity and steel plants in wet precipitation and suspended particulate matter in the MAPA was identified by the isotopic signatures of 208Pb/207Pb and 206Pb/207Pb. Moreover the analyses of the metallic elements allowed also to identify the contribution of other anthropic sources, such as steel plants and oil refinery.

  6. Elemental compositions of suspended particles released in glass manufacture

    Energy Technology Data Exchange (ETDEWEB)

    Mamuro, T; Mizohata, A; Kubota, T [Radiation Center of Osaka Prefecture, Sakai (Japan)

    1980-03-01

    Suspended particles released in glass manufacture were subjected to multielement analysis by means of instrumental neutron activation method and energy dispersive X-ray fluorescence spectrometry. Suspended particles emitted from glass manufacture generally consist of both particles emitted from glass fusion and those produced through fuel combustion (mainly oil combustion). Elemental compositions of suspended particles emitted from glass fusion were found to be strongly dependent on the kind and recipe of raw materials and additives. Of the various metallic elements involved in suspended particles emitted from glass fusion, the elements, As, Se, Cd, Sb, Pb and so on are regarded to produce the most serious air pollution. The amount of emission of these elements to the environment is, howerer, quite varied from manufacturer to manufacturer. The replacement of electric furnace by oil combustion in opal glass manufacture remarkably reduced the emission of metallic elements to the environment.

  7. Evaluating cleansing effects on trace elements and stable isotope values in feathers of oiled birds.

    Science.gov (United States)

    Valladares, Sonia; Moreno, Roćio; Jover, Lluis; Sanpera, Carola

    2010-01-01

    Feathers of seabirds are widely used as a nondestructive tissue for pollution monitoring of trace elements, as well as convenient samples for trophic ecology studies by means of stable isotope analysis (SIA). Nevertheless, feathers can be occasionally impregnated with oil from deliberate ship discharges and from massive oil spill accidents. The feather structure makes them effective traps for particles and are subject to external contamination. It is unknown to what extent the oil adhered to feathers can change trace element concentrations or stable isotope signatures. This study has two primary objectives: (1) to assess if there are differences between trace element concentrations and stable isotope signatures of oiled and clean feathers, and (2) to determine if the cleansing of oiled feathers using commonly applied techniques such as sodium hydroxide (NaOH) washes in combination with an organic solvent (hexane) is more effective than using NaOH alone. In order to do this, we analysed trace elements (Se, Hg, Pb, Cu and Zn) and stable isotopes (delta(13)C and delta(15)N) of individual feathers of yellow-legged gulls (Larus michahellis) which were affected by the 2002 Prestige oil spill in Galicia (NW Spain). Two sets of feathers were analysed, one group were oil-free (Control group) and the other had oil adhered to its surface (Oiled group). We expected to find differences between control and oiled feathers when cleaning exclusively with NaOH and no differences when using hexane. Our results did not show significant differences between Control and Oiled groups as a consequence of the cleansing method used. Unexpectedly, the additional cleansing with hexane resulted in decreasing selenium concentrations and increasing zinc and delta(15)N values in all groups of feathers.

  8. Magnesium and Titanium Isotopic Compositions of an Unusual Hibonite-Perovskite Refractory Inclusion from Allende: It Is Fun

    Science.gov (United States)

    Liu, M.-C.; Keller, L. P.; McKeegan, K. D.

    2016-01-01

    Introduction: Hibonite-rich refractory inclusions are among the first solids that formed in the solar nebula, and thus provide constraints on the earliest environment in the Solar System. An unusual hibonite-perovskite inclusion from Allende, SHAL, consists of a large (approximately 500 by 200 microns) single hibonite crystal and coexisting blocky perovskite (approximately 200 microns in size). The hibonite is characterized by chemical and oxygen isotopic compositions similar to those in the FUN (Fractionated and Unknown Nuclear anomalies) inclusion HAL. However, the rare earth element (REE) patterns measured at different spots of SHAL hibonite are highly variable, ranging from Group II-like (light REEs enriched relative to heavy REEs) to Group III-like (relatively flat with slight Eu depletions), but overall contrast largely with that of HAL, especially in the Ce and Yb abundances. This implies that SHAL hibonite formed and underwent distillation processes under more reducing conditions. Interestingly, the accompanying perovskite has uniform, unfractionated oxygen isotopic compositions (averaging delta (sup 17) O equals delta (sup 18) O equals -7 per mille) and REE abundances that are completely different from those of SHAL hibonite. This has been interpreted that perovskite and hibonite may not be co-genetic. Here we performed Al-Mg and Ti isotopic measurements of SHAL hibonite and perovskite to determine if the FUN characteristics are observed in these two isotope systems, and to further constrain the origin and evolution of SHAL. Results: Isotopic measurements of Al-Mg and Ti in SHAL were performed on the UCLA CAMECA ims-1290 ion microprobe by following the analytical protocols described in [1]. The Al-Mg and Ti data obtained in both terrestrial standards and SHAL hibonite and perovskite are shown below. Both SHAL hibonite and perovskite, despite very high (sup 27) Al to (sup 24) Mg ratios, are devoid of (sup 26) Mg excesses that can be attributed to the decay

  9. Proximate and mineral elements composition of five locally ...

    African Journals Online (AJOL)

    The proximate composition of the studied fruits were determined by the standard methods of Official Analytical Chemists, while the Mineral Elements (Ca and Mg) were analyzed using Atomic Absorption Spectrophotometry. The levels of Na+ and K+ were determined using Flame photometry and the level of P was ...

  10. Effect of Processing on the Elemental Composition of Selected Leafy ...

    African Journals Online (AJOL)

    The elemental composition of leaves of Vernonia amygdalina, Gnetum africana, Gongronema latifolium and Ocimum gratissimum subjected to different processing methods were investigated. Processing methods employed include oven drying, sun drying, fresh milling, steaming and a combination of these while the mineral ...

  11. Machining of Machine Elements Made of Polymer Composite Materials

    Science.gov (United States)

    Baurova, N. I.; Makarov, K. A.

    2017-12-01

    The machining of the machine elements that are made of polymer composite materials (PCMs) or are repaired using them is considered. Turning, milling, and drilling are shown to be most widely used among all methods of cutting PCMs. Cutting conditions for the machining of PCMs are presented. The factors that most strongly affect the roughness parameters and the accuracy of cutting PCMs are considered.

  12. Synthesis and properties of neutron deficient isotopes of elements around Z=100

    International Nuclear Information System (INIS)

    Antalic, S.

    2005-01-01

    In the presented Thesis work the results of spectroscopic studies of 246 Md, 247 Md, 254 Lr and 255 Lr decay chains are given. These isotopes were produced using heavy ion induced fusion reactions of 40 Ar + 209 Bi and 48 Ca + 209 Bi as a part of the long term project aimed to study spectroscopy properties of superheavy elements. The experiments were performed at velocity filter SHIP, placed at the central beam line of the UNILAC accelerator at GSI Darmstadt in Germany. The work also gives a basic overview of research in the region of superheavy elements, description of the used experimental setup and shows the usual analysis methods used in spectroscopic studies in the region of elements around Z ∼ 100. The results were obtained using α, α - γ spectroscopy methods and recoil - α, α - α correlations search. Although these isotopes have been known for a longer time, no detailed spectroscopy investigation were performed so far and only rough information was known. Beside the improved precision of known data, this work gives a new information about the decay properties of these isotopes. This give us the possibility to build a decay schemes for mentioned decay chains. (author)

  13. Variations in isotopic compositions of chlorine in evaporation-controlled salt lake brines of Qaidam Basin, China

    Digital Repository Service at National Institute of Oceanography (India)

    Xiao, Ying-kai; Liu, Wei-guo; Zhou, Y.M.; Wang, Yun-hui; Shirodkar, P.V.

    The variations in the isotopic compositions of chlorine in evaporation-controlled saline lake brines were determined by using an improved procedure for precise measurement of chlorine isotopes based on Cs sub(2) Cl sup(+) ion by thermal ionization...

  14. Boron, lithium and methane isotope composition of hyperalkaline waters (Northern Apennines, Italy): Terrestrial serpentinization or mixing with brine?

    International Nuclear Information System (INIS)

    Boschetti, Tiziano; Etiope, Giuseppe; Pennisi, Maddalena; Romain, Millot; Toscani, Lorenzo

    2013-01-01

    Highlights: ► First data on boron and lithium isotope on waters from ophiolites are described. ► High boron and lithium isotope composition may be related to terrestrial serpentinization. ► Methane isotope data show unusual biotic signature. - Abstract: Spring waters issuing from serpentinized ultramafic rocks of the Taro-Ceno Valleys (Northern Apennine, Emilia-Romagna region, Italy) were analyzed for major element, trace element and dissolved gas concentrations and δ 11 B, δ 7 Li, δ 18 O(H 2 O), δ 2 H(H 2 O), δ 13 C(CH 4 ) and δ 2 H(CH 4 ) isotope compositions. Similar to other springs worldwide that issue from serpentinites, the chemical composition of the waters evolves with water–rock interaction from Ca-HCO 3 , through Mg-HCO 3 and ultimately to a hyperalkaline Na-(Ca)-OH composition. Most of the Ca- and Mg-HCO 3 springs have δ 11 B ranging between +16.3‰ and +23.7‰, consistent with the range of low P–T serpentinites. Very high δ 11 B in two springs from Mt. Prinzera (PR10: +39‰; PR01: +43‰) can be related to isotopic fractionation during secondary phase precipitation, as also inferred from δ 7 Li values. In contrast to typical abiogenic isotope signatures of CH 4 from serpentinized rocks, dissolved CH 4 from the Taro-Ceno hyperalkaline springs has an apparent biotic (thermogenic and/or mixed thermogenic-microbial) signature with δ 13 C(CH 4 ) ranging from −57.5‰ to −40.8‰, which is similar to that of hydrocarbons from production wells and natural seeps in adjacent hydrocarbon systems. The data suggest that CH 4 in the hyperalkaline springs investigated in this study may derive from organic matter of the sedimentary (flysch and arenaceous) formations underlying the ophiolite unit. However, small amounts of H 2 were detected in one hyperalkaline spring (PR10), but for two springs with very low CH 4 concentrations (PR01 and UM15) the δ 2 H value could not be measured, so the occurrence of some abiotic CH 4 cannot be excluded

  15. Seasonal dynamics of stable isotopes and element ratios in authigenic calcites during their precipitation and dissolution, Sacrower See (northeastern Germany

    Directory of Open Access Journals (Sweden)

    Bernd ZOLITSCHKA

    2009-08-01

    Full Text Available The seasonal evolution of chemical and physical water properties as well as particle fluxes was monitored in Sacrower See (northeastern Germany during two consecutive years (Oct 2003 - Oct 2005. Additonally, we measured δ18O and δ13C as well as Sr:Ca and Mg:Ca ratios of authigenic calcites that were collected in sequencing sediment traps in order to disentangle environmental and climatic factors controlling these parameters. In particular, our aim was to find out if element ratios and the isotopic composition of calcites reflect changes in water and air temperatures. Lake water is highly enriched in 18O (-1.3 to -2.5‰ VSMOW with an evaporative increase of 0.6‰ during summer. Values are 5-6‰ more positive than groundwater values and 4-5‰ more positive than long-term weighted annual means of precipitation. During spring and summer, high amounts of dissolved phosphate cause eutrophic conditions and calcite precipitation in isotopic disequilibrium. Measured values are depleted in 18O by 2 to 10‰ compared to calculated equilibrium values. Resuspension and partial dissolution of calcite in the water column contribute to this isotopic divergence in summer and autumn as δ18Oca and δ13C values increased in the hypolimnion during this time. Mg:Ca and Sr:Ca ratios are altered by dissolution as well. In the hypolimnion these ratios were higher than in the epilimnion. Another reason for the huge deviation between measured and theoretical δ18Oca values during summer is the occurrence of large amounts of Phacotus lenticularis in the carbonate fraction. High amounts of Phacotus lead to more negative δ18Oca and more positive δ13C values. Several characteristics of δ18Oca and δ13C are also reflected by Mg:Ca and Sr:Ca ratios and isotopic composition of oxygen and carbon were influenced by the onset and stability of stratification. Especially the earlier onset of stratification in 2005 caused higher sediment fluxes and more positive carbon and

  16. Spatial patterns of throughfall isotopic composition at the event and seasonal timescales

    Science.gov (United States)

    Allen, Scott T.; Keim, Richard F.; McDonnell, Jeffrey J.

    2015-03-01

    Spatial variability of throughfall isotopic composition in forests is indicative of complex processes occurring in the canopy and remains insufficiently understood to properly characterize precipitation inputs to the catchment water balance. Here we investigate variability of throughfall isotopic composition with the objectives: (1) to quantify the spatial variability in event-scale samples, (2) to determine if there are persistent controls over the variability and how these affect variability of seasonally accumulated throughfall, and (3) to analyze the distribution of measured throughfall isotopic composition associated with varying sampling regimes. We measured throughfall over two, three-month periods in western Oregon, USA under a Douglas-fir canopy. The mean spatial range of δ18O for each event was 1.6‰ and 1.2‰ through Fall 2009 (11 events) and Spring 2010 (7 events), respectively. However, the spatial pattern of isotopic composition was not temporally stable causing season-total throughfall to be less variable than event throughfall (1.0‰; range of cumulative δ18O for Fall 2009). Isotopic composition was not spatially autocorrelated and not explained by location relative to tree stems. Sampling error analysis for both field measurements and Monte-Carlo simulated datasets representing different sampling schemes revealed the standard deviation of differences from the true mean as high as 0.45‰ (δ18O) and 1.29‰ (d-excess). The magnitude of this isotopic variation suggests that small sample sizes are a source of substantial experimental error.

  17. Isotopic composition of carbon of natural gases in the sedimentary basins of Kamchatka and Chukotka

    Energy Technology Data Exchange (ETDEWEB)

    Lobkov, V.A.; Kudriavtseva, E.I.

    1981-01-01

    A study was carried out on the chemical and isotopic compositions of carbon of natural gases, which are prospective for oil and gas structures. An isotopic composition of the carbon of gases, covered by wells in possible oil and gas bearing basins (Eastern Kamchatka Central Kamchatka, Western Kamchatka, Anadyrsk, and Khatyrsk), created by terrigenic rock of the cretaceous, paleogenic, and neogenic ages, with dimensions of three to six kilometers, is presented. Investigation is made of the isotopic carbon of methane, ethane, and propane in 36 gas specimens. The plan of the distribution of the tested structures is shown, and an analysis is given of the chemical and isotopic composition of carbon of the prospected areas of Kamchatka and Chukotka and the interconnection of the isotopic composition of the carbon of methane with ethane and propane. A supposition is made concerning the existence of a single equilibrious volumetric system of CH/sub 4/--C/sub 2/H/sub 6/--C/sub 3/H/sub 8/--CO/sub 2/, in which ethane and propane are by-products, and owing to this, equilibrium establish according to this more slowly. The study of the isotopic composition of carbon of methane shows, that at various areas of depth formation of hydrocarbon gases is different. A conclusion is made that the gases formed at high temperatures. This points to a significant distance in the vertical migration of gases in the given region.

  18. Stable isotopic composition of perchlorate and nitrate accumulated in plants: Hydroponic experiments and field data.

    Science.gov (United States)

    Estrada, Nubia Luz; Böhlke, J K; Sturchio, Neil C; Gu, Baohua; Harvey, Greg; Burkey, Kent O; Grantz, David A; McGrath, Margaret T; Anderson, Todd A; Rao, Balaji; Sevanthi, Ritesh; Hatzinger, Paul B; Jackson, W Andrew

    2017-10-01

    Natural perchlorate (ClO 4 - ) in soil and groundwater exhibits a wide range in stable isotopic compositions (δ 37 Cl, δ 18 O, and Δ 17 O), indicating that ClO 4 - may be formed through more than one pathway and/or undergoes post-depositional isotopic alteration. Plants are known to accumulate ClO 4 - , but little is known about their ability to alter its isotopic composition. We examined the potential for plants to alter the isotopic composition of ClO 4 - in hydroponic and field experiments conducted with snap beans (Phaseolus vulgaris L.). In hydroponic studies, anion ratios indicated that ClO 4 - was transported from solutions into plants similarly to NO 3 - but preferentially to Cl - (4-fold). The ClO 4 - isotopic compositions of initial ClO 4 - reagents, final growth solutions, and aqueous extracts from plant tissues were essentially indistinguishable, indicating no significant isotope effects during ClO 4 - uptake or accumulation. The ClO 4 - isotopic composition of field-grown snap beans was also consistent with that of ClO 4 - in varying proportions from irrigation water and precipitation. NO 3 - uptake had little or no effect on NO 3 - isotopic compositions in hydroponic solutions. However, a large fractionation effect with an apparent ε ( 15 N/ 18 O) ratio of 1.05 was observed between NO 3 - in hydroponic solutions and leaf extracts, consistent with partial NO 3 - reduction during assimilation within plant tissue. We also explored the feasibility of evaluating sources of ClO 4 - in commercial produce, as illustrated by spinach, for which the ClO 4 - isotopic composition was similar to that of indigenous natural ClO 4 - . Our results indicate that some types of plants can accumulate and (presumably) release ClO 4 - to soil and groundwater without altering its isotopic characteristics. Concentrations and isotopic compositions of ClO 4 - and NO 3 - in plants may be useful for determining sources of fertilizers and sources of ClO 4 - in their growth

  19. Petrogenesis and origin of the Upper Jurassic-Lower Cretaceous magmatism in Central High Atlas (Morocco): Major, trace element and isotopic (Sr-Nd) constraints

    Science.gov (United States)

    Essaifi, Abderrahim; Zayane, Rachid

    2018-01-01

    During an uplift phase, which lasted ca. 40 Ma, from the Late Jurassic (165 Ma) to the Early Cretaceous (125 Ma), transitional to moderately alkaline magmatic series were emplaced in the Central High Atlas. The corresponding magmatic products include basaltic lava flows erupted within wide synclines and intrusive complexes composed of layered mafic intrusions and monzonitic to syenitic dykes emplaced along narrow anticlinal ridges. The igneous rock sequence within the intrusive complexes is composed of troctolites, olivine-gabbros, oxide-gabbros, monzonites and syenites. The chemical compositions of the various intrusive rocks can be accounted for by crystal accumulation, fractional crystallization and post-magmatic remobilization. The evolution from the troctolites to the syenites was mainly controlled by a fractional crystallization process marked by early fractionation of olivine, plagioclase and clinopyroxene, followed by separation of biotite, amphibole, apatite, and Ti-magnetite. Hydrothermal activity associated with emplacement of the intrusions within the Jurassic limestones modified the elemental and the Sr isotopic composition of the hydrothermally altered rocks In particular the monzonitic to syenitic dykes underwent an alkali metasomatism marked by depletion in K and Rb and enrichment in Na and Sr. As a result, their Sr isotopic composition was shifted towards higher initial Sr isotopic ratios (0.7067-0.7075) with respect to the associated gabbros (0.7036-0.7046). On the contrary, the Nd isotopic compositions were preserved from isotope exchange with the limestones and vary in a similar range to those of the gabbros (+1.6 < εNdi < +4.1). The isotopic and the trace element ratios of the uncontaminated samples were used to constrain the source characteristics of this magmatism. The Sr-Nd isotopic data and the incompatible element ratios (e.g. La/Nb, Zr/Nb, Th/U, Ce/Pb) are consistent with generation from an enriched upper mantle similar to an ocean

  20. Effect of changes in environment on the variation in elemental composition of airborne dust

    International Nuclear Information System (INIS)

    Miyamoto, Yutaka; Saito, Yoko; Magara, Masaaki; Sakurai, Satoshi; Usuda, Shigekazu

    2004-01-01

    For the research on environmental impact caused by nuclear activities, we are developing monitoring technique to measure radioactivity, isotopic and elemental composition in airborne dust, which contains nuclear materials and radioactive elements released from nuclear facilities. We focus on its elimination process such as wash-out by rainfall and adsorption to plants in the processes which affect the amounts and composition of the airborne dust. Recently at JAERI-Tokai, a number of pine trees to arrest sand shifting were cut down. This gave us a good opportunity to examine the effect of presence of the trees on the variation in elemental composition of airborne dust, therefore, we collected dust samples with a high-volume sampler before and after felling the trees, and analyzed them by means of instrumental neutron activation analysis. No change was observed in the amount, Al- and Sc- concentrations of the dust collected before and after felling the trees nearby the sampling site. There were correlations between the elemental concentration of Zn and that of Sb, and between Zn and As. These elements might originate from some by-products of social activities such as fly ashes. If found that the concentration of these elements after felling the trees decrease to 60% of the concentration before the works. The histograms of concentration of Cl in the airborne samples were compiled using the samples which the average of relative humidity in the period of the sample collection was 70-80%. The Cl concentration in the airdust after felling the trees at the seaside was three times higher than that concentration before the works. It found that the trees can eliminate more effectively the aerosols such as sea-salt than soil from the atmosphere. (author)

  1. Elemental composition at different points of the rainwater harvesting system

    International Nuclear Information System (INIS)

    Morrow, A.C.; Dunstan, R.H.; Coombes, P.J.

    2010-01-01

    Entry of contaminants, such as metals and non-metals, into rainwater harvesting systems can occur directly from rainfall with contributions from collection surfaces, accumulated debris and leachate from storage systems, pipes and taps. Ten rainwater harvesting systems on the east coast of Australia were selected for sampling of roof runoff, storage systems and tap outlets to investigate the variations in rainwater composition as it moved throughout the system, and to identify potential points of contribution to elemental loads. A total of 26 elements were screened at each site. Iron was the only element which was present in significantly higher concentrations in roof runoff samples compared with tank tap samples (P < 0.05). At one case study site, results suggested that piping and tap material can contribute to contaminant loads of harvested rainwater. Increased loads of copper were observed in hot tap samples supplied by the rainwater harvesting system via copper piping and a storage hot water system (P < 0.05). Similarly, zinc, lead, arsenic, strontium and molybdenum were significantly elevated in samples collected from a polyvinyl chloride pipe sampling point that does not supply household uses, compared with corresponding roof runoff samples (P < 0.05). Elemental composition was also found to vary significantly between the tank tap and an internal cold tap at one of the sites investigated, with several elements fluctuating significantly between the two outlets of interest at this site, including potassium, zinc, manganese, barium, copper, vanadium, chromium and arsenic. These results highlighted the variability in the elemental composition of collected rainwater between different study sites and between different sampling points. Atmospheric deposition was not a major contributor to the rainwater contaminant load at the sites tested. Piping materials, however, were shown to contribute significantly to the total elemental load at some locations.

  2. Constraints on the nature of the projectile using siderophile elements and triple-oxygen isotopes: Zhamanshin impact structure, Kazakhstan

    Czech Academy of Sciences Publication Activity Database

    Jonášová, Šárka; Ackerman, Lukáš; Žák, Karel; Skála, Roman; Magna, T.; Pack, A.; Deutsch, A.

    2016-01-01

    Roč. 51, SI, Supplement 1 (2016), A358-A358 ISSN 1086-9379. [Annual Meeting of the Meteoritical Society /79./. 07.08.2016-12.08.2016, Berlin] Institutional support: RVO:67985831 Keywords : impact glass * irghizites * geochemistry * meteoritic component * siderophile elements * osmium isotopes * triple-oxygen Isotopes * Zhamanshin Subject RIV: DD - Geochemistry

  3. Iron Isotopic Compositions of Troilite (FeS) Inclusions from Iron Meteorites

    Energy Technology Data Exchange (ETDEWEB)

    Cook, David L.; Schönbächler, Maria, E-mail: david.cook@erdw.ethz.ch [Institut für Geochemie und Petrologie, ETH Zürich, Clausiusstrasse 25, 8092 Zürich (Switzerland)

    2017-10-01

    We report non-mass-dependent Fe isotopic data for troilite (FeS) inclusions from 10 iron meteorites, representing both non-magmatic (IAB) and magmatic groups (IIAB, IIIAB, IVA). No resolvable variations are present in the most neutron-rich isotope ({sup 58}Fe), but small deficits (≈−0.1 ε ) in {sup 56}Fe were observed in several inclusions. With the exception of several Ca–Al-rich inclusions in primitive meteorites, these are the first reported non-mass-dependent variations in Fe isotopes for material formed in the early solar system. Nucleosynthetic variations in Ni isotopes were previously reported in these same samples. The effects in Fe isotopes are not correlated with those in Ni, which suggests that the origins of the isotopic variations are decoupled from one another. The {sup 56}Fe deficits may represent incomplete mixing of the precursor dust in the protoplanetary disk. Alternatively, a parent body process (e.g., irradiation by galactic cosmic rays) may have modified the Fe isotopic compositions of some inclusions, which initially had homogeneous Fe isotopic compositions.

  4. Features of adsorbed chemical elements and their isotopes distribution in iodine air filters AU-1500 of nuclear power plant

    International Nuclear Information System (INIS)

    Neklyudov, I.M.; Dovbnya, A.N.; Dikiy, N.P.; Ledenyov, O.P.; Lyashko, Yu.V.

    2013-01-01

    The main aim of research is to investigate the physical features of spatial distribution of the adsorbed chemical elements and their isotopes in the granular filtering medium in the iodine air filters of the type of AU-1500 in the forced-exhaust ventilation at the nuclear power plant. The ?-activation analysis method is applied to accurately characterize the distribution of the adsorbed radioactive chemical elements and their isotopes in the granular filtering medium in the AU-1500 iodine air filter after its long term operation at the nuclear power plant. The typical spectrum of the detected chemical elements and their isotopes in the AU-1500 iodine air filter, which was exposed by the irradiation of bremsstrahlung gamma-quantum producing by the accelerating electrons in the tantalum target, are obtained. The spatial distributions of the detected chemical element 127 I and some other chemical elements and their isotopes in the layer of absorber, which was made of the cylindrical coal granules of the type of SKT-3, in the AU-1500 iodine air filter are also researched. The possible influences by the standing wave of air pressure in the iodine air filter on the spatial distribution of the chemical elements and their isotopes in the iodine air filter are discussed. The comprehensive analysis of obtained research results on the distribution of the adsorbed chemical elements and their isotopes in the absorber of iodine air filter is performed.

  5. Stable calcium isotope composition of a pedogenic carbonate in forested ecosystem: the case of the needle fibre calcite (NFC).

    Science.gov (United States)

    Milliere, Laure; Verrecchia, Eric; Gussone, Nikolaus

    2014-05-01

    Calcium (Ca), carbon (C) and oxygen (O) are important elements in terrestrial environment, as their biogeochemical cycles are directly related to the storage of atmospheric carbon. Nevertheless, contrarily to C and O, Ca isotope composition has been only poorly studied in the terrestrial carbonates. Needle Fibre Calcite (NFC) is one of the most common pedogenic carbonates, unless its origin is still under debate. Recent studies explain its formation by precipitation inside fungal hyphae. Due to this possible biogenic origin, NFC can be considered as a potential bridge between the biochemistry (precipitation inside organic structure) and geochemistry (pedogenic carbonate related to soil conditions) of the Ca. Thus, the study of the Ca isotope composition of NFC seem to be of first interest in order to shed light on the behaviour of Ca in terrestrial environment, especially when precipitation of secondary carbonates is involved. The sampling site is situated in the Swiss Jura Mountains and has been chosen due to a previous complete study of the C and O isotope composition of NFC in relation to the ecosystem, which represent a good precondition for the understanding of the NFC Ca isotope signatures in this context. In this study, the implication of the fungi in the origin of NFC is investigated, by comparing the Ca isotope composition of NFC and a purely physicochemical calcite cement (LCC), both precipitated in the same environment. The δ44Ca signature of NFC and LCC crystals were used to determine possible differences of the precipitation rate during their formation. NFC and LCC have similar δ18O composition and are supposed to precipitate at the same temperature (Milliere et al., 2011a). Thus the study of Ca isotope composition of NFC seems to demonstrate that the elongated shape of the calcite needle can be explained by different precipitation processes than the rhombohedric calcite crystals precipitated in the same environment; and more precisely, the specific

  6. Characteristics of lead isotope ratios and elemental concentrations in PM 10 fraction of airborne particulate matter in Shanghai after the phase-out of leaded gasoline

    Science.gov (United States)

    Zheng, Jian; Tan, Mingguang; Shibata, Yasuyuki; Tanaka, Atsushi; Li, Yan; Zhang, Guilin; Zhang, Yuanmao; Shan, Zuci

    The stable lead (Pb) isotope ratios and the concentrations of 23 elements, including heavy metals and toxic elements, were measured in the PM 10 airborne particle samples collected at seven monitoring sites in Shanghai, China, to evaluate the current elemental compositions and local airborne Pb isotope ratio characteristics. Some source-related samples, such as cement, coal and oil combustion dust, metallurgic dust, vehicle exhaust particles derived from leaded gasoline and unleaded gasoline, and polluted soils were analyzed for their Pb content and isotope ratio and compared to those observed in PM 10 samples. Airborne Pb concentration ranged from 167 to 854 ng/m 3 in the seven monitored sites with an average of 515 ng/m 3 in Shanghai, indicating that a high concentration of Pb remains in the air after the phasing out of leaded gasoline. Lead isotopic compositions in airborne particles ( 207Pb/ 206Pb, 0.8608±0.0018; 208Pb/ 206Pb, 2.105±0.005) are clearly distinct from the vehicle exhaust particles ( 207Pb/ 206Pb, 0.8854±0.0075; 208Pb/ 206Pb, 2.145±0.006), suggesting that the automotive lead is not currently the major component of Pb in the air. By using a binary mixing equation, a source apportionment based on 207Pb/ 206Pb ratios, indicates that the contribution from automotive emission to the airborne Pb is around 20%. The Pb isotope ratios obtained in the source-related samples confirmed that the major emission sources are metallurgic dust, coal combustion, and cement.

  7. The first investigation of Wilms' tumour atomic structure-nitrogen and carbon isotopic composition as a novel biomarker for the most individual approach in cancer disease

    Science.gov (United States)

    Taran, Katarzyna; Frączek, Tomasz; Sikora-Szubert, Anita; Sitkiewicz, Anna; Młynarski, Wojciech; Kobos, Józef; Paneth, Piotr

    2016-01-01

    The paper describes a novel approach to investigating Wilms' tumour (nephroblastoma) biology at the atomic level. Isotope Ratio Mass Spectrometry (IRMS) was used to directly assess the isotope ratios of nitrogen and carbon in 84 Wilms' tumour tissue samples from 28 cases representing the histological spectrum of nephroblastoma. Marked differences in nitrogen and carbon isotope ratios were found between nephroblastoma histological types and along the course of cancer disease, with a breakout in isotope ratio of the examined elements in tumour tissue found between stages 2 and 3. Different isotopic compositions with regard to nitrogen and carbon content were observed in blastemal Wilms' tumour, with and without focal anaplasia, and in poorly- and well-differentiated epithelial nephroblastoma. This first assessment of nitrogen and carbon isotope ratio reveals the previously unknown part of Wilms' tumour biology and represents a potential novel biomarker, allowing for a highly individual approach to treating cancer. Furthermore, this method of estimating isotopic composition appears to be the most sensitive tool yet for cancer tissue evaluation, and a valuable complement to established cancer study methods with prospective clinical impact. PMID:27732932

  8. Measurements of Plutonium isotopes and the search for super-heavy elements via AMS

    International Nuclear Information System (INIS)

    Wallner, A.; Steier, P.; Golser, R.; Knie, K.; Kutschera, W.; Priller, A.; Hrnecek, E.; Jakopic, R.; Korschinek, G.

    2006-01-01

    Full text: Accelerator Mass Spectrometry (AMS) - being independent on the half-life of a radionuclide - provides a technique to determine isotope ratios with the highest sensitivity and allows the measurement of radionuclides over a wide dynamic range of concentration levels. A combination of AMS, Alpha Spectrometry and Liquid Scintillation Counting was used for the determination of the complete information on isotope ratios of Plutonium isotopes in different environmental reference samples (e.g. from the atolls of Mururoa and Fangataufa) and samples contaminated from nuclear reprocessing. Results for the isotopic ratios of the samples will be shown and the capabilities and detection limits achievable for determination of Pu will be discussed. The long-lived 244 Pu (t 1/2 = 80 Ma) and 247 Cm (t 1/2 = 15.6 Ma) have a very interesting application in astrophysics by detecting possible supernova-produced 244 Pu and 247 Cm in terrestrial archives. The expected extremely small concentrations of 244 Pu makes AMS the favorite method. The actual search for such long-lived extraterrestrial radionuclides and possible implications will be presented. The same method has also been explored for a pinprick-search of long-lived super-heavy elements in the mass region above Z=100. (author)

  9. Measurement of natural carbon isotopic composition of acetone in human urine.

    Science.gov (United States)

    Yamada, Keita; Ohishi, Kazuki; Gilbert, Alexis; Akasaka, Mai; Yoshida, Naohiro; Yoshimura, Ryoko

    2016-02-01

    The natural carbon isotopic composition of acetone in urine was measured in healthy subjects using gas chromatography-combustion-isotope ratio mass spectrometry combined with headspace solid-phase microextraction (HS-SPME-GC-C-IRMS). Before applying the technique to a urine sample, we optimized the measurement conditions of HS-SPME-GC-C-IRMS using aqueous solutions of commercial acetone reagents. The optimization enabled us to determine the carbon isotopic compositions within ±0.2 ‰ of precision and ±0.3‰ of error using 0.05 or 0.2 mL of aqueous solutions with acetone concentrations of 0.3-121 mg/L. For several days, we monitored the carbon isotopic compositions and concentrations of acetone in urine from three subjects who lived a daily life with no restrictions. We also monitored one subject for 3 days including a fasting period of 24 h. These results suggest that changes in the availability of glucose in the liver are reflected in changes in the carbon isotopic compositions of urine acetone. Results demonstrate that carbon isotopic measurement of metabolites in human biological samples at natural abundance levels has great potential as a tool for detecting metabolic changes caused by changes in physiological states and disease.

  10. Sulfur contents and sulfur-isotope compositions of thiotrophic symbioses in bivalve molluscs and vestimentiferan worms

    Science.gov (United States)

    Vetter, R.D.; Fry, B.

    1998-01-01

    Total sulfur (S(TOT)), elemental sulfur (S??) and sulfur-isotope compositions (??34S) of marine animals were analyzed to determine whether these chemical characteristics could help distinguish animals with a sulfur-based, thiotrophic nutrition from animals whose nutrition is based on methanotrophy or on more normal consumption of phytoplankton-derived organic matter. The presence of S??was almost entirely confined to the symbiont-containing tissues of thiotrophs, but was sometimes undetectable in thiotrophic species where sulfide availability was probably low. When S??contents were subtracted, the remaining tissue-sulfur concentrations were similar for all nutritional groups. ??34S values were typically lower for thiotrophs than for other groups, although there was overlap in methanotroph and thiotroph values at some sites. Field evidence supported the existence of small to moderate (1 to 10???)34S fractionations in the uptake of sulfides and metabolism of thiosulfate. In general, a total sulfur content of >3% dry weight, the presence of elemental sulfur, and ??34S values less than + 5??? can be used to infer a thiotrophic mode of nutrition.

  11. Elemental composition and oxidation of chamber organic aerosol

    Directory of Open Access Journals (Sweden)

    P. S. Chhabra

    2011-09-01

    Full Text Available Recently, graphical representations of aerosol mass spectrometer (AMS spectra and elemental composition have been developed to explain the oxidative and aging processes of secondary organic aerosol (SOA. It has been shown previously that oxygenated organic aerosol (OOA components from ambient and laboratory data fall within a triangular region in the f44 vs. f43 space, where f44 and f43 are the ratios of the organic signal at m/z 44 and 43 to the total organic signal in AMS spectra, respectively; we refer to this graphical representation as the "triangle plot." Alternatively, the Van Krevelen diagram has been used to describe the evolution of functional groups in SOA. In this study we investigate the variability of SOA formed in chamber experiments from twelve different precursors in both "triangle plot" and Van Krevelen domains. Spectral and elemental data from the high-resolution Aerodyne aerosol mass spectrometer are compared to offline species identification analysis and FTIR filter analysis to better understand the changes in functional and elemental composition inherent in SOA formation and aging. We find that SOA formed under high- and low-NOx conditions occupy similar areas in the "triangle plot" and Van Krevelen diagram and that SOA generated from already oxidized precursors allows for the exploration of areas higher on the "triangle plot" not easily accessible with non-oxidized precursors. As SOA ages, it migrates toward the top of the triangle along a path largely dependent on the precursor identity, which suggests increasing organic acid content and decreasing mass spectral variability. The most oxidized SOA come from the photooxidation of methoxyphenol precursors which yielded SOA O/C ratios near unity. α-pinene ozonolysis and naphthalene photooxidation SOA systems have had the highest degree of mass closure in previous chemical characterization studies and also show the

  12. Chromium isotope composition of reducing and anoxic sediments from the Peru Margin and Cariaco Basin

    Science.gov (United States)

    Gueguen, B.; Planavsky, N.; Wang, X.; Algeo, T. J.; Peterson, L. C.; Reinhard, C. T.

    2014-12-01

    Chromium isotope systematics in marine sediments are now being used as a new redox proxy of the modern and ancient Earth's surface. Chromium is primarily delivered to the oceans by riverine inputs through weathering of Cr(III)-rich minerals present in the continental crust and oxidation of insoluble Cr(III) to soluble Cr(VI) species. Since oxidation-reduction reactions fractionate Cr isotopes whereby oxidized Cr(VI) species are preferentially enriched in heavy Cr isotopes, the Cr isotope composition of marine sediments may be useful tracers of redox conditions at the Earth's surface through geological time. Chromium is quantitatively removed in organic-rich sediments where reducing conditions prevail and promote reduction of Cr(VI) to Cr(III), and thus, these sediments should capture the ambient seawater Cr isotope composition. However, the isotopic composition of modern organic-rich sediments is poorly documented so far, and this step is essential for further modeling the global oceanic Cr isotope mass balance and assessing the effects of sedimentation and post-depositional processes on the marine Cr isotopes archive. In this study, we have characterized modern marine organic-rich sediments for their Cr isotope composition (δ53/52Cr) from two different settings, the Peru margin upwelling zone and the anoxic Cariaco Basin (Venezuela). Chromium isotopes were measured on a MC-ICP-MS (Nu Plasma) using a double-spike correction method. The authigenic fraction of shallow samples from the Peru margin sedimentary sequence with a high Total Organic Carbon (TOC) content (>10 wt%) yield an average δ53/52Crauthigenic value of +0.67 ±0.05 ‰ (2sd). However, although this value is close to the seawater value (Atlantic Ocean) and to Cariaco basin sediments (~ +0.6 ‰), reducing sediments from the Peru margin are on average isotopically slightly heavier, especially in samples having a low authigenic fraction and a low TOC content (δ53/52Crauthigenic values up to +1.30

  13. Analytical and statistical analysis of elemental composition of lichens

    International Nuclear Information System (INIS)

    Calvelo, S.; Baccala, N.; Bubach, D.; Arribere, M.A.; Riberio Guevara, S.

    1997-01-01

    The elemental composition of lichens from remote southern South America regions has been studied with analytical and statistical techniques to determine if the values obtained reflect species, growth forms or habitat characteristics. The enrichment factors are calculated discriminated by species and collection site and compared with data available in the literature. The elemental concentrations are standardized and compared for different species. The information was statistically processed, a cluster analysis was performed using the three first principal axes of the PCA; the three groups formed are presented. Their relationship with the species, collection sites and the lichen growth forms are interpreted. (author)

  14. Calibration of a finite element composite delamination model by experiments

    DEFF Research Database (Denmark)

    Gaiotti, M.; Rizzo, C.M.; Branner, Kim

    2013-01-01

    This paper deals with the mechanical behavior under in plane compressive loading of thick and mostly unidirectional glass fiber composite plates made with an initial embedded delamination. The delamination is rectangular in shape, causing the separation of the central part of the plate into two...... distinct sub-laminates. The work focuses on experimental validation of a finite element model built using the 9-noded MITC9 shell elements, which prevent locking effects and aiming to capture the highly non linear buckling features involved in the problem. The geometry has been numerically defined...

  15. Elemental composition changes in citrus affected by the CVC disease

    International Nuclear Information System (INIS)

    Nadai Fernandes de, A.A.; Tagliaferro, F.S.; Turra, C.; Franca de, E.J.; Bacchi, M.A.

    2008-01-01

    The citrus variegated chlorosis (CVC) disease results in serious economical losses for the Brazilian citriculture. The influence of CVC disease on the elemental composition of citrus plants was investigated. Leaves of sweet orange varieties Hamlin, Pera Rio and Valencia were collected from healthy and CVC-affected trees for chemical characterization by instrumental neutron activation analysis (INAA). Significant differences between healthy and CVC-affected leaves were identified for Ca, Ce, Co, Eu, Fe, K, La, Na, Nd, Rb, Sc and Sm. Rare earth elements presented consistently higher mass fractions in the healthy leaves. (author)

  16. Stable Isotopic Composition of Rainfall in Western Cameroon

    Energy Technology Data Exchange (ETDEWEB)

    Ketchemen-Tandia, B.; Ngo Boum, S.; Ebonji Seth, C. R.; Nkoue Ndong, G. R.; Wonkam, C. [Universite de Douala, Douala (Cameroon); Huneau, F. [Universite de Bordeaux, EA Georessources and Environnement, Talence (France); Celle-Jeanton, H. [Clermont Universite, Clermont-Ferrand (France)

    2013-07-15

    Monthly rainfall collected at the douala station (Western cameroon) from 2006 to 2008 was analysed for oxygen-18 and deuterium content. The dataset, which is now integrated into the GNIP database, was compared to the local groundwater record in order to define the input function of regional hydrosystems. The isotope data displays a wide range of values from -0.59 to -6.14 per mille for oxygen-18 and from -7.75 to -38.8 per mille for deuterium, closely following the GMWL (global Meteoric Water line), suggesting that rain formation processes occurred under isotopic equilibrium conditions between the condensate and the corresponding vapour. No significant evaporation tendency was found. The comparison with the previous studies in the area provides a realistic pattern of isotope concentrations in both surface and groundwater throughout Cameroon. (author)

  17. Oxygen isotopic composition of mammal bones as a new tool for studying ratios of paleoenvironmental water and paleoclimates

    International Nuclear Information System (INIS)

    Longinelli, A.

    1984-04-01

    The purpose of this study is to try to establish quantitative relationships between the average oxygen isotopic composition of local meteoric water, the oxygen isotopic composition of mammal body water and the oxygen isotopic composition of phosphate in mammal bones. These relationships, after calibration of the method on living specimens, would allow quantitative paleoclimatological research based on the measurement of delta 18 O(PO 4 3- ) of fossil mammal bones

  18. Transition of the Isotopic Composition of Leaf Water to the Isotopic Steady State in Soybean and Corn

    Science.gov (United States)

    Kim, K.; Lee, X.; Welp, L. R.

    2007-12-01

    The isotope composition of leaf water (δL) plays an important role in the isotopic water and carbon fluxes between terrestrial plants and the atmosphere. The objective of this study is to improve our understanding of environmental and biological controls on the transition of δL to steady state through laboratory experiments. Plants (soybean, Glycine max; corn, Zea mays) were grown hydroponically with water of a known isotopic content in a greenhouse. On the day of the experiment, they were first moved to ambient environment in full sunlight for at least 6 hr and then into a dark container inside the lab for up to 48 hr in which water vapor isotope ratios, temperature, and humidity were controlled. This arrangement created a step change in the forcing on the plant isotopic exchange. Leaves were sampled prior to the transfer to the dark container and 6 more times every 4 - 12 hr over the experiment. In the first set of experiments, humidity inside the container was saturated to mimic dew events in field conditions. In the second set, humidity was controlled at approximately 95%. Water from the leaf samples was extracted by a vacuum line and was analyzed for both δD and δ18O. The dataset will allow us to evaluate leaf water isotopic theories by exploring the transitions of δL in response to the step change. Specifically, we are interested in whether the stomatal opening is an effective pathway for gaseous exchange in total darkness and how the transitional behaviors of δL differ between the C3 and C4 photosynthesis pathways.

  19. Determination of the hydrogen isotopic compositions of organic materials and hydrous minerals using thermal combustion laser spectroscopy.

    Science.gov (United States)

    Koehler, Geoff; Wassenaar, Leonard I

    2012-04-17

    Hydrogen isotopic compositions of hydrous minerals and organic materials were measured by combustion to water, followed by optical isotopic analysis of the water vapor by off-axis integrated cavity output spectroscopy. Hydrogen and oxygen isotopic compositions were calculated by numerical integration of the individual isotopologue concentrations measured by the optical spectrometer. Rapid oxygen isotope exchange occurs within the combustion reactor between water vapor and molecular oxygen so that only hydrogen isotope compositions may be determined. Over a wide range in sample sizes, precisions were ±3-4 per mil. This is comparable but worse than continuous flow-isotope ratio mass spectroscopy (CF-IRMS) methods owing to memory effects inherent in water vapor transfer. Nevertheless, the simplicity and reduced cost of this analysis compared to classical IRMS or CF-IRMS methods make this an attractive option to determine the hydrogen isotopic composition of organic materials where the utmost precision or small sample sizes are not needed.

  20. Modelling and Mapping Oxygen-18 Isotope Composition of Precipitation in Spain for Hydrologic and Climatic Applications

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez-Arevalo, J.; Diaz-Teijeiro, M. F. [Centro de Estudios y Experimentacion de Obras Publicas (CEDEX), Madrid (Spain); Castano, S. [Geological Survey of Spain (IGME), Madrid (Spain)

    2013-07-15

    A simple multiple regression model based on two geographic factors (latitude and elevation) has been developed that reproduces reasonably well the spatial distribution of the current mean oxygen-18 isotope composition in precipitation over spain. In a preliminary analysis, additional geographic and climatic factors do not improve the performance of the model. A continuous digital map of oxygen-18 isotope composition in precipitation has been produced by combining the polynomial model with a digital elevation model using GIS tools. Application of the resulting map to several groundwater case studies in spain has shown it to be useful as a reference of the input function to recharge. Further validation of the model, and further testing of its usefulness in surface hydrology and climatic studies, is ongoing through comparison of model results with isotope data from the GNIP database and from isotope studies in hydrogeology and climate change taking place in spain. (author)

  1. Fe isotope composition of bulk chondrules from Murchison (CM2): Constraints for parent body alteration, nebula processes and chondrule-matrix complementarity

    Science.gov (United States)

    Hezel, Dominik C.; Wilden, Johanna S.; Becker, Daniel; Steinbach, Sonja; Wombacher, Frank; Harak, Markus

    2018-05-01

    Chondrules are a major constituent of primitive meteorites. The formation of chondrules is one of the most elusive problems in cosmochemistry. We use Fe isotope compositions of chondrules and bulk chondrites to constrain the conditions of chondrule formation. Iron isotope compositions of bulk chondrules are so far only known from few studies on CV and some ordinary chondrites. We studied 37 chondrules from the CM chondrite Murchison. This is particularly challenging, as CM chondrites contain the smallest chondrules of all chondrite groups, except for CH chondrites. Bulk chondrules have δ56Fe between -0.62 and +0.24‰ relative to the IRMM-014 standard. Bulk Murchison has as all chondrites a δ56Fe of 0.00‰ within error. The δ56Fe distribution of the Murchison chondrule population is continuous and close to normal. The width of the δ56Fe distribution is narrower than that of the Allende chondrule population. Opaque modal abundances in Murchison chondrules is in about 67% of the chondrules close to 0 vol.%, and in 33% typically up to 6.5 vol.%. Chondrule Al/Mg and Fe/Mg ratios are sub-chondritic, while bulk Murchison has chondritic ratios. We suggest that the variable bulk chondrule Fe isotope compositions were established during evaporation and recondensation prior to accretion in the Murchison parent body. This range in isotope composition was likely reduced during aqueous alteration on the parent body. Murchison has a chondritic Fe isotope composition and a number of chondritic element ratios. Chondrules, however, have variable Fe isotope compositions and chondrules and matrix have complementary Al/Mg and Fe/Mg ratios. In combination, this supports the idea that chondrules and matrix formed from a single reservoir and were then accreted in the parent body. The formation in a single region also explains the compositional distribution of the chondrule population in Murchison.

  2. Trace elements and Pb isotopes in soils and sediments impacted by uranium mining

    Energy Technology Data Exchange (ETDEWEB)

    Cuvier, A., E-mail: alicia.cuvier@hotmail.fr [ECOLAB, Université de Toulouse, CNRS, INPT, UPS, Toulouse (France); IRSN/PRP-ENV/SESURE/Laboratoire d' études radioécologiques en milieu continental et marin, BP 1, 13108 Saint Paul Lez Durance Cedex (France); Pourcelot, L. [IRSN/PRP-ENV/SESURE/Laboratoire d' études radioécologiques en milieu continental et marin, BP 1, 13108 Saint Paul Lez Durance Cedex (France); Probst, A. [ECOLAB, Université de Toulouse, CNRS, INPT, UPS, Toulouse (France); Prunier, J. [Observatoire Midi-Pyrénées, laboratoire Géosciences Environnement Toulouse, CNRS/IRD/Université Paul Sabatier, 14 avenue Edouard Belin, 31400 Toulouse (France); Le Roux, G., E-mail: gael.leroux@ensat.fr [ECOLAB, Université de Toulouse, CNRS, INPT, UPS, Toulouse (France)

    2016-10-01

    The purpose of this study is to evaluate the contamination in As, Ba, Co, Cu, Mn, Ni, Sr, V, Zn and REE, in a high uranium activity (up to 21,000 Bq ∙ kg{sup −1}) area, downstream of a former uranium mine. Different geochemical proxies like enrichment factor and fractions from a sequential extraction procedure are used to evaluate the level of contamination, the mobility and the availability of the potential contaminants. Pb isotope ratios are determined in the total samples and in the sequential leachates to identify the sources of the contaminants and to determine the mobility of radiogenic Pb in the context of uranium mining. In spite of the large uranium contamination measured in the soils and the sediments (EF ≫ 40), trace element contamination is low to moderate (2 < EF < 5), except for Ba (5 < EF < 15), due to the precipitation of barium sulfate resulting from mining activities. Most of the trace elements are associated with the most mobile fractions of the sediments/soils, implying an enhanced potential availability. Even if no Pb enrichment is highlighted, the Pb isotopic signature of the contaminated soils is strongly radiogenic. Measurements performed on the sequential leachates reveal inputs of radiogenic Pb in the most mobile fractions of the contaminated soil. Inputs of low-mobile radiogenic Pb from mining activities may also contribute to the Pb signature recorded in the residual phase of the contaminated samples. We demonstrate that Pb isotopes are efficient tools to trace the origin and the mobility of the contaminants in environments affected by uranium mining. - Highlights: • Contamination of soils is evidenced by a multiproxy approach. • Enrichment factors highlight a low contamination except for U, S and Ba. • Pb isotope ratios point out inputs of radiogenic Pb from the mine. • Radiogenic Pb is mainly in the acid-soluble and the reducible fractions.

  3. Factors that control the stable carbon isotopic composition of methane produced in an anoxic marine sediment

    Science.gov (United States)

    Alperin, M. J.; Blair, Neal E.; Albert, D. B.; Hoehler, T. M.; Martens, C. S.

    1993-01-01

    The carbon isotopic composition of methane produced in anoxic marine sediment is controlled by four factors: (1) the pathway of methane formation, (2) the isotopic composition of the methanogenic precursors, (3) the isotope fractionation factors for methane production, and (4) the isotope fractionation associated with methane oxidation. The importance of each factor was evaluated by monitoring stable carbon isotope ratios in methane produced by a sediment microcosm. Methane did not accumulate during the initial 42-day period when sediment contained sulfate, indicating little methane production from 'noncompetitive' substrates. Following sulfate depletion, methane accumulation proceeded in three distinct phases. First, CO2 reduction was the dominant methanogenic pathway and the isotopic composition of the methane produced ranged from -80 to -94 per thousand. The acetate concentration increased during this phase, suggesting that acetoclastic methanogenic bacteria were unable to keep pace with acetate production. Second, acetate fermentation became the dominant methanogenic pathway as bacteria responded to elevated acetate concentrations. The methane produced during this phase was progressively enriched in C-13, reaching a maximum delta(C-13) value of -42 per thousand. Third, the acetate pool experienced a precipitous decline from greater than 5 mM to less than 20 micro-M and methane production was again dominated by CO2 reduction. The delta(C-13) of methane produced during this final phase ranged from -46 to -58 per thousand. Methane oxidation concurrent with methane production was detected throughout the period of methane accumulation, at rates equivalent to 1 to 8 percent of the gross methane production rate. Thus methane oxidation was too slow to have significantly modified the isotopic signature of methane. A comparison of microcosm and field data suggests that similar microbial interactions may control seasonal variability in the isotopic composition of methane

  4. Chemical composition and mineral elements of edible insects (at ...

    African Journals Online (AJOL)

    The Chemical Composition and Mineral Elements of two edible insects' larvae and termite soldiers were assayed. Their ash content were between 1.01% and 7.50%. The legless larva (LS) had 28.52% fat, while the solider ant had 7.14% and the Legged larva (LG) had 1.50%. The white ant (SA) had 15.61% protein while ...

  5. Element for separating gaseous isotopes into at least two fractions and with a separating basket consisting of several separating elements

    International Nuclear Information System (INIS)

    Grossstuck, W.; Schafer, R.

    1985-01-01

    A separating element for gaseous isotopes into two fractions, and consisting of several elongated separating chips with a row of entry openings for the process gas at one side of the chips and a row of exit openings for the heavy fraction at the other side of the chips, with exit openings for the light fraction at the edges of the chips, and of two tubes holding the chips and having at least one chamber, with said tubes being connected by means of connecting elements, and equipped with entry and exit openings on their contact surfaces, with said entry and exit openings arranged in rows in a longitudinal direction of the chips, and for simplifying of installation and construction, this invention provides that the chips are arranged in a longitudinal direction to the tubes, with their sides abutting directly against the smooth contact surfaces of the tubes, and whereby the connecting elements are positioned in one row in the center of the two tubes

  6. Towards improved modeling of steel-concrete composite wall elements

    International Nuclear Information System (INIS)

    Vecchio, Frank J.; McQuade, Ian

    2011-01-01

    Highlights: → Improved analysis of double skinned steel concrete composite containment walls. → Smeared rotating crack concept applied in formulation of new analytical model. → Model implemented into finite element program; numerically stable and robust. → Models behavior of shear-critical elements with greater ease and improved accuracy. → Accurate assessments of strength, deformation and failure mode of test specimens. - Abstract: The Disturbed Stress Field Model, a smeared rotating crack model for reinforced concrete based on the Modified Compression Field Theory, is adapted to the analysis of double-skin steel-concrete wall elements. The computational model is then incorporated into a two-dimensional nonlinear finite element analysis algorithm. Verification studies are undertaken by modeling various test specimens, including panel elements subject to uniaxial compression, panel elements subjected to in-plane shear, and wall specimens subjected to reversed cyclic lateral displacements. In all cases, the analysis model is found to provide accurate calculations of structural load capacities, pre- and post-peak displacement responses, post-peak ductility, chronology of damage, and ultimate failure mode. Minor deficiencies are found in regards to the accurate portrayal of faceplate buckling and the effects of interfacial slip between the faceplates and the concrete. Other aspects of the modeling procedure that are in need of further research and development are also identified and discussed.

  7. 61 stable isotope compositions of organic carbon and contents of ...

    African Journals Online (AJOL)

    Mgina

    isotope record from Lake Ndutu shows a general downcore decrease in δ. 13C values ... in bulk δ13C of the terrestrial biomass in the tropics may ... CO2, temperature, moisture conditions and ... A map showing location of sampling sites of Ngorongoro Crater, Lake Ndutu and .... the Lakes Makat and Masek records cannot.

  8. Carbon and oxygen isotope compositions of the carbonate facies

    Indian Academy of Sciences (India)

    The Vindhyan sedimentary succession in central India spans a wide time bracket from the Paleopro- terozoic to the Neoproterozoic period.Chronostratigraphic significance of stable carbon and oxygen isotope ratios of the carbonate phase in Vindhyan sediments has been discussed in some recent studies.However,the ...

  9. The Serchio River catchment, northern Tuscany: Geochemistry of stream waters and sediments, and isotopic composition of dissolved sulfate

    International Nuclear Information System (INIS)

    Cortecci, Gianni; Dinelli, Enrico; Boschetti, Tiziano; Arbizzani, Paola; Pompilio, Loredana; Mussi, Mario

    2008-01-01

    The Serchio River and its tributaries in northern Tuscany were investigated for the chemical and isotopic compositions of waters and bed sediments. Bedrocks are mostly limestone/dolomite and siliciclastics, thermal spring systems are present in the catchment, and the main industrial activity is represented by paper-mills. Main results obtained are: (1) major ions in solution appear to be basically controlled by precipitation and lithology, as well as subordinately by direct inputs of thermal springs, (2) human influence on metals in the waters along the main Serchio and Lima rivers is indicated at a number of sites by increases in concentration compared to the chemical composition of upstream tributaries, (3) S and O isotope compositions delineate two main sources for aqueous SO 4 2- , that is dissolution of Triassic evaporite (directly or via thermal springs) and oxidation of sulfide dispersed in siliciclastic rocks. Anthropogenic contributions are probable, but they cannot be quantitatively assessed. Only SO 4 2- in the notoriously polluted Ozzeri tributary is suspected to be largely anthropogenic, and (4) the chemical composition of bed sediments is mainly influenced by lithology, apart from a number of technogenic elements in the upper part of the Serchio River and in some tributaries. Contamination possibly occurs at other sites, but geochemical indications are weak

  10. Elemental and Isotopic Incorporation into the Aragonitic Shells of Arctica Islandica: Insights from Temperature Controlled Experiments

    Science.gov (United States)

    Wanamaker, A. D.; Gillikin, D. P.

    2014-12-01

    The long-lived ocean quahog, Arctica islandica, is a fairly well developed and tested marine proxy archive, however, the utility of elemental ratios in A. islandica shell material as environmental proxies remains questionable. To further evaluate the influence of seawater temperature on elemental and isotopic incorporation during biomineralization, A. islandica shells were grown at constant temperatures under two regimes during a 16-week period from March 27 to July 21, 2011. Seawater from the Darling Marine Center in Walpole, Maine was pumped into temperature and flow controlled tanks that were exposed to ambient food and salinity conditions. A total of 20 individual juvenile clams with an average shell height of 36 mm were stained with calcein (a commonly used biomarker) and cultured at 10.3 ± 0.3 °C for six weeks. After this, shell heights were measured and the clams were again stained with calcein and cultured at 15.0 ± 0.4 °C for an additional 9.5 weeks. The average shell growth during the first phase of the experiment was 2.4 mm with a linear extension rate of 0.40 mm/week. The average shell growth during the second phase of the experiment was 3.2 mm with an extension rate of 0.34 mm/week. Average salinity values were 30.2 ± 0.7 and 30.7 ±0.7 in the first and second phases of the experiment, respectively. Oxygen isotopes from the cultured seawater were collected throughout the experiment and provide the basis for establishing if shells grew in oxygen isotopic equilibrium. Elemental ratios (primarily Ba/Ca, Mg/Ca, Sr/Ca) in the aragonitic shells were determined via laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS), while stable oxygen and carbon isotope ratios were measured using continuous flow isotope ratio mass spectrometry. Continuous sampling within and across the temperature conditions (from 10 °C to 15 °C) coupled with the calcein markings provides the ability to place each sample into a precise temporal framework. The

  11. Elemental composition of urban aerosol collected in Florence, Italy

    International Nuclear Information System (INIS)

    Lucarelli, F.; Mando, P.A.; Nava, S.; Prati, P.; Zucchiatti, A.

    2000-01-01

    An extensive investigation is in progress aiming at the characterisation of the air particulate composition in Florence. The aim is to determine the aerosol elemental concentrations as well to identify pollution sources. For our investigation, we use the external PIXE-PIGE beam facility of the Van de Graaff accelerator of INFN at the Physics Department of the Florence University. We report here an overview of the results of the PIXE analysis of a long temporal series (about 1 yr) of PM 10 particulate collected on Millipore filters on a daily basis in three different sites (characterised by different urban settings). Daily concentrations of more than 20 elements have been obtained. From the observed elemental concentrations seasonal variation were found. A relevant decrease of S, Pb and Br levels has been found with respect to 10 yr ago. Four main sources (traffic, sulphates, soil-dust and wind-transported sea-salt) have been extracted with the help of factor analysis

  12. Assessing the effects of the Prestige oil spill on the European shag (Phalacrocorax aristotelis): Trace elements and stable isotopes

    International Nuclear Information System (INIS)

    Sanpera, Carola; Valladares, Sonia; Moreno, Rocio; Ruiz, Xavier; Jover, Lluis

    2008-01-01

    The Prestige oil spill resulted in the mortality of several seabird species on the Atlantic NW coast of Spain. Shag casualties were particularly relevant, since populations are resident in the area the whole year round and because of several features which make them highly vulnerable to environmental hazards. Ecological catastrophes give us the opportunity of collecting samples which, otherwise, would be difficult to obtain. We examine the potential of shag corpses as bioindicators of inorganic pollution and the possible factors of variability, such as biological traits (sex, age) or nutrition status. We determined trace elements (Hg, Se, Cr, Pb, Zn and Cu) and isotopic signatures ( 15 N, 13 C) in soft tissues (muscle, liver) and in primary feathers formed at different times (before and after the Prestige) in individuals of known sex and age, collected at the time of the Prestige disaster. These were compared with data from another group of shags trapped accidentally in fishing gear in 2005. Our results did not seem to be affected by sex or age on any of the analysed variables. The higher nitrogen isotopic signatures in the soft tissues of the Prestige shags may be related to the nutrition stress caused by a poorer body condition, which is also reflected in increasing levels of some metals in the liver. This isotopic enrichment was also observed in newly forming feathers when compared to the old ones. On the other hand, the lower δ 15 N and Hg values in shag feathers from 2005 point to a shift in feeding resources to prey of lower trophic levels. We found that feather features (being an inert tissue and having a conservative composition), if combined with careful dating and chemical analysis, offer a very useful tool to evaluate temporal and spatial changes in seabird ecology in relation to pollution events

  13. Assessing the effects of the Prestige oil spill on the European shag (Phalacrocorax aristotelis): Trace elements and stable isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Sanpera, Carola [Dept. Biologia Animal, Facultat de Biologia, Universitat de Barcelona, Diagonal 645, 08028 Barcelona (Spain)], E-mail: csanpera@ub.edu; Valladares, Sonia; Moreno, Rocio; Ruiz, Xavier [Dept. Biologia Animal, Facultat de Biologia, Universitat de Barcelona, Diagonal 645, 08028 Barcelona (Spain); Jover, Lluis [Dept. Salut Publica, Facultat de Medicina, Universitat de Barcelona, Casanova 143, 08036 Barcelona (Spain)

    2008-12-15

    The Prestige oil spill resulted in the mortality of several seabird species on the Atlantic NW coast of Spain. Shag casualties were particularly relevant, since populations are resident in the area the whole year round and because of several features which make them highly vulnerable to environmental hazards. Ecological catastrophes give us the opportunity of collecting samples which, otherwise, would be difficult to obtain. We examine the potential of shag corpses as bioindicators of inorganic pollution and the possible factors of variability, such as biological traits (sex, age) or nutrition status. We determined trace elements (Hg, Se, Cr, Pb, Zn and Cu) and isotopic signatures ({sup 15}N, {sup 13}C) in soft tissues (muscle, liver) and in primary feathers formed at different times (before and after the Prestige) in individuals of known sex and age, collected at the time of the Prestige disaster. These were compared with data from another group of shags trapped accidentally in fishing gear in 2005. Our results did not seem to be affected by sex or age on any of the analysed variables. The higher nitrogen isotopic signatures in the soft tissues of the Prestige shags may be related to the nutrition stress caused by a poorer body condition, which is also reflected in increasing levels of some metals in the liver. This isotopic enrichment was also observed in newly forming feathers when compared to the old ones. On the other hand, the lower {delta}{sup 15}N and Hg values in shag feathers from 2005 point to a shift in feeding resources to prey of lower trophic levels. We found that feather features (being an inert tissue and having a conservative composition), if combined with careful dating and chemical analysis, offer a very useful tool to evaluate temporal and spatial changes in seabird ecology in relation to pollution events.

  14. Finite element modelling and analysis of composites toecaps

    International Nuclear Information System (INIS)

    Yang, C C; Duhovic, M; Lin, R J T; Bhattacharyya, D

    2009-01-01

    Composite toe-caps have attracted considerable attention due to their advantageous properties over traditional metallic toe-caps. However, the anisotropic properties of composite materials also make the toe-cap performance more complex to analyse. This project aims at developing a Finite Element (FE) model for composite toe-caps with the aid of compression testing data. The geometry of the toe-cap was first scanned and imported into an FEA software package to create a workable FE model. The method was then validated by comparing the FE model with experimental results of steel toe-caps. Manufacturing, modelling and testing of custom-made composite toe-cap samples were then carried out. Modelling outputs of composite toe-caps were compared with compression test data for validation. The stress distributions and deformations of the toe-caps were also analysed. Modelling of the steel and composite toe-caps was realized using LS-DYNA Solver and PrePost (registered) . All FE analyses were modelled with reference to European Standards. The developed FE models can in the future be used to model toe-caps with various materials to determine the effects of fibre orientation relating to structural strength, and to achieve structural optimisation.

  15. Chemical and sulphur isotope compositions of pyrite in the ...

    Indian Academy of Sciences (India)

    sulphide mineralization and their chemical evo- lution in relative .... properties and chemical compositions. Electron ..... from the sulphide lode provide clues to the chang- ing fluid ..... Raymond O L 1996 Pyrite composition and ore geneis in.

  16. Databook of the isotopic composition of spent fuel in light water reactors

    International Nuclear Information System (INIS)

    Naito, Yoshitaka; Kurosawa, Masayoshi; Kaneko, Toshiyuki.

    1993-03-01

    In the framework of the activity of the nuclide production evaluation WG in the sigma committee, we summarized the measurement data of the isotopic composition of LWR spent fuels necessary to evaluate the accuracy of the burnup calculation codes. The collected data were arranged to be classified into the irradiation history of the fuel samples, the composition of the fuel assemblies, the sampling position and the isotopic composition of the fuel samples, in order to supply the information necessary to the benchmark calculation. This report describes the data collected from the 13 LWRs including the 9 LWRs (5 PWR and 4 BWR) in Europe and the USA, the 4 LWRs (2 PWR and 2 BWR) in Japan. Finally, the study on the burnup characteristics of the U, Pu isotopes is described. (author)

  17. Plutonium isotopes in the atmosphere of Central Europe: Isotopic composition and time evolution vs. circulation factors

    Energy Technology Data Exchange (ETDEWEB)

    Kierepko, Renata, E-mail: Renata.Kierepko@ifj.edu.pl [Institute of Nuclear Physics, Polish Academy of Sciences, Krakow (Poland); Mietelski, Jerzy W. [Institute of Nuclear Physics, Polish Academy of Sciences, Krakow (Poland); Ustrnul, Zbigniew [Jagiellonian University, Krakow (Poland); Institute of Meteorology and Water Management, National Research Institute, Krakow (Poland); Anczkiewicz, Robert [Institute of Geological Sciences, Polish Academy of Sciences, Krakow (Poland); Wershofen, Herbert [Physikalisch-Technische Bundesanstalt, Braunschweig (Germany); Holgye, Zoltan [National Radiation Protection Institute, Prague (Czech Republic); Kapała, Jacek [Medical University of Bialystok (Poland); Isajenko, Krzysztof [Central Laboratory for Radiological Protection, Warsaw (Poland)

    2016-11-01

    This paper reports evidence of Pu isotopes in the lower part of the troposphere of Central Europe. The data were obtained based on atmospheric aerosol fraction samples collected from four places in three countries (participating in the informal European network known as the Ring of Five (Ro5)) forming a cell with a surface area of about 200,000 km{sup 2}. We compared our original data sets from Krakow (Poland, 1990–2007) and Bialystok (Poland, 1991–2007) with the results from two other locations, Prague (Czech Republic; 1997–2004) and Braunschweig (Germany; 1990–2003) to find time evolution of the Pu isotopes. The levels of the activity concentration for {sup 238}Pu and for {sup (239} {sup +} {sup 240)}Pu were estimated to be a few and some tens of nBq m{sup −} {sup 3}, respectively. However, we also noted some results were much higher (even about 70 times higher) than the average concentration of {sup 238}Pu in the atmosphere. The achieved complex data sets were used to test a new approach to the problem of solving mixing isotopic traces from various sources (here up to three) in one sample. Results of our model, supported by mesoscale atmospheric circulation parameters, suggest that Pu from nuclear weapon accidents or tests and nuclear burnt-up fuel are present in the air. - Highlights: • Evidence of Pu isotopes in the lower part of the troposphere of Central Europe • The effective annual doses associated with Pu inhalation • New approach to the problem of solving mixed Pu origins in one sample (3SM) • Relationship between Pu isotopes activity concentration and circulation factors.

  18. Food authenticity studies via multi-elemental and isotopic pattern using inductively coupled plasma mass spectrometry

    International Nuclear Information System (INIS)

    Katona, R.; Brunner, M.; Abranko, L.; Prohaska, T.; Stefanka, Z.

    2009-01-01

    Full text: The aim of our study has been the development of an analytical method based on Sr isotope and elemental fingerprint analysis for discriminating food samples from different geographical origin. Several types of foods were involved in the investigation representing different stages of food processing such as pulverized spicy paprika (sparsely processed food product) and wine samples (processed product). Independent inorganic mass spectrometric techniques like ICP-SFMS, ICP-CCMS, and MC-ICPMS were used for method validation and investigation of the geographical origin. The advantage and limitations of the developed methods are discussed critically. (author)

  19. Production of transplutonium elements in the high flux isotope reactor (HFIR)

    International Nuclear Information System (INIS)

    Bigelow, J.E.; Corbett, B.L.; King, L.J.; McGuire, S.C.; Sims, T.M.

    1980-01-01

    The techniques described have been demonstrated to be adequate to predict the contents of transplutonium element production targets which have been irradiated in the HFIR. The deviations, at least for isotopes of mass 253 or less, are generally within the usual analytical uncertainties, or else are for isiotopes which are of little overall import to the program. Work is especially needed to get a better picture of the production of 250 Cm, 254 Es, 255 Es, and ultimately 257 Fm, since researchers are frequently stating their interest in obtaining larger quantities of these rare and difficult-to-produce nuclides

  20. The carbon isotopic compositions of individual compounds from ancient and modern depositional environments

    Energy Technology Data Exchange (ETDEWEB)

    Freeman, K.H.

    1991-01-01

    This work examines factors influencing the isotopic compositions of individual compounds and, consequently, that of preserved sedimentary organic matter. Specifically, isotope effects associated with reactions resulting in the production and degradation of organic matter in the water column and reactions affecting preservation during diagenesis are considered in three projects. The first documents the preservation of the isotopic compositions of hydrocarbons altered by diagenetic reaction. Isotopic compositions of structurally-related polycyclic aromatic hydrocarbons (PAH) from the Messel Shale show little variation with increased unsaturation. The influence of environmental conditions on the isotopic composition of sedimentary organic carbon is documented by a comparison of the {delta}{sup 13}C of hydrocarbons in the marine Julia Creek Oil Shale and the lacustrine Condor Oil Shale. A model is proposed for identifying relative degrees of oxygenation and productivity within a paleoenvironment based on the observed {sup 13}C contents of biomarkers. Effects of processes proposed in the environmental model are documented by an examination of hydrocarbons from the waters and sediments of the Black Sea and of the Cariaco Trench. Sources of individual compounds are identified by comparison of their {sup 13}C content with that predicted for autotrophic biomass calculated from the concentration and {sup 13}C content of CO{sub 2}(aq) in the surface waters.

  1. Evaluating climate model performance in the tropics with retrievals of water isotopic composition from Aura TES

    Science.gov (United States)

    Field, Robert; Kim, Daehyun; Kelley, Max; LeGrande, Allegra; Worden, John; Schmidt, Gavin

    2014-05-01

    Observational and theoretical arguments suggest that satellite retrievals of the stable isotope composition of water vapor could be useful for climate model evaluation. The isotopic composition of water vapor is controlled by the same processes that control water vapor amount, but the observed distribution of isotopic composition is distinct from amount itself . This is due to the fractionation that occurs between the abundant H216O isotopes (isotopologues) and the rare and heavy H218O and HDO isotopes during evaporation and condensation. The fractionation physics are much simpler than the underlying moist physics; discrepancies between observed and modeled isotopic fields are more likely due to problems in the latter. Isotopic measurements therefore have the potential for identifying problems that might not be apparent from more conventional measurements. Isotopic tracers have existed in climate models since the 1980s but it is only since the mid 2000s that there have been enough data for meaningful model evaluation in this sense, in the troposphere at least. We have evaluated the NASA GISS ModelE2 general circulation model over the tropics against water isotope (HDO/H2O) retrievals from the Aura Tropospheric Emission Spectrometer (TES), alongside more conventional measurements. A small ensemble of experiments was performed with physics perturbations to the cumulus and planetary boundary layer schemes, done in the context of the normal model development process. We examined the degree to which model-data agreement could be used to constrain a select group of internal processes in the model, namely condensate evaporation, entrainment strength, and moist convective air mass flux. All are difficult to parameterize, but exert strong influence over model performance. We found that the water isotope composition was significantly more sensitive to physics changes than precipitation, temperature or relative humidity through the depth of the tropical troposphere. Among the

  2. The isotopic composition of methane in the stratosphere: high-altitude balloon sample measurements

    Directory of Open Access Journals (Sweden)

    T. Röckmann

    2011-12-01

    Full Text Available The isotopic composition of stratospheric methane has been determined on a large suite of air samples from stratospheric balloon flights covering subtropical to polar latitudes and a time period of 16 yr. 154 samples were analyzed for δ13C and 119 samples for δD, increasing the previously published dataset for balloon borne samples by an order of magnitude, and more than doubling the total available stratospheric data (including aircraft samples published to date. The samples also cover a large range in mixing ratio from tropospheric values near 1800 ppb down to only 250 ppb, and the strong isotope fractionation processes accordingly increase the isotopic composition up to δ13C = −14‰ and δD = +190‰, the largest enrichments observed for atmospheric CH4 so far. When analyzing and comparing kinetic isotope effects (KIEs derived from single balloon profiles, it is necessary to take into account the residence time in the stratosphere in combination with the observed mixing ratio and isotope trends in the troposphere, and the range of isotope values covered by the individual profile. The isotopic composition of CH4 in the stratosphere is affected by both chemical and dynamical processes. This severely hampers interpretation of the data in terms of the relative fractions of the three important sink mechanisms (reaction with OH, O(1D and Cl. It is shown that a formal sink partitioning using the measured data severely underestimates the fraction removed by OH, which is likely due to the insensitivity of the measurements to the kinetic fractionation in the lower stratosphere. Full quantitative interpretation of the CH4 isotope data in terms of the three sink reactions requires a global model.

  3. Spurious and functional correlates of the isotopic composition of a generalist across a tropical rainforest landscape

    Directory of Open Access Journals (Sweden)

    Poirson Evan K

    2009-11-01

    Full Text Available Abstract Background The isotopic composition of generalist consumers may be expected to vary in space as a consequence of spatial heterogeneity in isotope ratios, the abundance of resources, and competition. We aim to account for the spatial variation in the carbon and nitrogen isotopic composition of a generalized predatory species across a 500 ha. tropical rain forest landscape. We test competing models to account for relative influence of resources and competitors to the carbon and nitrogen isotopic enrichment of gypsy ants (Aphaenogaster araneoides, taking into account site-specific differences in baseline isotope ratios. Results We found that 75% of the variance in the fraction of 15N in the tissue of A. araneoides was accounted by one environmental parameter, the concentration of soil phosphorus. After taking into account landscape-scale variation in baseline resources, the most parsimonious model indicated that colony growth and leaf litter biomass accounted for nearly all of the variance in the δ15N discrimination factor, whereas the δ13C discrimination factor was most parsimoniously associated with colony size and the rate of leaf litter decomposition. There was no indication that competitor density or diversity accounted for spatial differences in the isotopic composition of gypsy ants. Conclusion Across a 500 ha. landscape, soil phosphorus accounted for spatial variation in baseline nitrogen isotope ratios. The δ15N discrimination factor of a higher order consumer in this food web was structured by bottom-up influences - the quantity and decomposition rate of leaf litter. Stable isotope studies on the trophic biology of consumers may benefit from explicit spatial design to account for edaphic properties that alter the baseline at fine spatial grains.

  4. Changes of the water isotopic composition in unsaturated soils

    International Nuclear Information System (INIS)

    Feurdean, Victor; Feurdean, Lucia

    2001-01-01

    Based on the spatial and temporal variations of the stable isotope content in precipitation - as input in subsurface - and the mixing processes, the deuterium content in the water that moves in unsaturated zones was used to determine the most conducive season to recharge, the mechanisms for infiltration of snow or rain precipitation in humid, semi-arid or arid conditions, the episodic cycles of infiltration water mixing with the already present soil water and water vapor and whether infiltration water is or is not from local precipitation. Oscillations in the isotopic profiles of soil moisture can be used to estimate the following aspects: where piston or diffusive flow is the dominant mechanisms of water infiltration; the average velocities of the water movement in vadose zone; the influence of vegetation cover, soil type and slope exposure on the dynamics of water movement in soil; the conditions required for infiltration such as: the matrix, gravity, pressure and osmotic potentials during drainage in unsaturated soil. (authors)

  5. Isotopic separation of nitrogen 15. Influence of the gaseous phase composition

    International Nuclear Information System (INIS)

    Lacoste, Germain; Routie, Rene; Mahenc, Jean

    1977-01-01

    A study has been made on the gas phase composition effect on the isotopic separation of nitrogen 15 for the two HNO 3 -NO and N 2 O 3 -NO systems. It was shown that the changes in composition of the gas phases could account for the increase in the overall separation; most accuracy, measurements of isotopic concentration along the separation column and of total enrichment exhibit how important are the reactions of oxydo-reduction between the two phases in such process [fr

  6. Isotope Compositions Of Mekong River Flow Water In The South Of Vietnam

    International Nuclear Information System (INIS)

    Nguyen Kien Chinh; Huynh Long; Le Danh Chuan; Nguyen Van Nhien; Tran Thi Bich Lien

    2008-01-01

    As a part of the Research Contract No. VIE/12569, isotope composition of Mekong river flow water in the South of Vietnam has been monitored to provide information on water origin and residence times, surface-groundwater exchange in the monitoring area. According to the primary results obtained, a seasonal variation as well as the dependence on local precipitation and on the river water level of isotopic composition of two distributaries of Mekong river water have been observed. At the same time a slight change on season of tritium in rivers water and the difference between tritium content in local rainy water and river water has been recorded. (author)

  7. Determining Isotopic Composition of Dissolved Nitrate Using Bacterial Denitrification Followed by Laser Spectroscopy

    International Nuclear Information System (INIS)

    Yan Tiezhu; Lee Zhi Yi, Amelia; Heiling, Maria; Weltin, Georg; Toloza, Arsenio; Resch, Christian

    2016-01-01

    Nitrate (NO 3 - ) pollution is a prevalent problem that can cause water quality degradation and eutrophication of water bodies. Quantifying the nitrogen and oxygen isotopic composition of nitrates will allow for better identification of their potential sources, which in turn will assist in remediation of contaminated water and the designing of future water management practices. In this research bacterial denitrification followed by laser spectroscopy are used to determine isotopic composition of δ 15 N and δ 18 O of dissolved nitrates. The objective of the project is to establish a standard operating procedure (SOP) that outlines the best practices for both methods in sequence and designed to be used as a technical guideline

  8. Element enrichment and U-series isotopic characteristics of the hydrothermal sulfides at Jade site in the Okinawa Trough

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The geochemical and U-series isotopic characteristics of hydrothermal sulfide samples from the Jade site (127°04.5′E, 27°15′N, water depth 1300-1450 m) at Jade site in the Okinawa Trough were analyzed. In the hydrothermal sulfide samples bearing sulfate (samples HOK1 and HOK2), the LREEs are relatively enriched. All the hydrothermal sulfide samples except HOK1 belong to Zn-rich hydrothermal sulfide. In comparison with Zn-rich hydrothermal sulfides from other fields, the contents of Zn, Pb, Ag, Cd, Au and Hg are higher, the contents of Fe, Al, Cr, Co, Ni, Sr, Te, Cs, Ti and U lower, and the 210Pb radioactivity ratios and 210Pb/Pb ratios very low. In the hydrothermal sulfide mainly composed of sphalerite, the correlations between rare elements Hf and U, and Hf and Mn as well as that between dispersive elements Ga and Zn, are strongly positive; also the contents of Au and Ag are related to Fe-sulfide, because the low temperature promotes enrichment of Au and Ag. Meanwhile, the positive correlations between Fe and Bi and between Zn and Cd are not affected by the change of mineral assemblage. Based on the 210Pb/Pb ratios of hydrothermal sulfide samples (3.99×10-5-5.42×10?5), their U isotopic composition (238U content 1.15-2.53 ppm, 238U activity 1.07-1.87 dpm/g, 234U activity 1.15-2.09 dpm/g and 234U/238U ratio 1.07-1.14) and their 232Th and 230Th contents are at base level, and the chronological age of hydrothermal sulfide at Jade site in the Okinawa Trough is between 200 and 2000 yr.

  9. Authigenic oxide Neodymium Isotopic composition as a proxy of seawater: applying multivariate statistical analyses.

    Science.gov (United States)

    McKinley, C. C.; Scudder, R.; Thomas, D. J.

    2016-12-01

    The Neodymium Isotopic composition (Nd IC) of oxide coatings has been applied as a tracer of water mass composition and used to address fundamental questions about past ocean conditions. The leached authigenic oxide coating from marine sediment is widely assumed to reflect the dissolved trace metal composition of the bottom water interacting with sediment at the seafloor. However, recent studies have shown that readily reducible sediment components, in addition to trace metal fluxes from the pore water, are incorporated into the bottom water, influencing the trace metal composition of leached oxide coatings. This challenges the prevailing application of the authigenic oxide Nd IC as a proxy of seawater composition. Therefore, it is important to identify the component end-members that create sediments of different lithology and determine if, or how they might contribute to the Nd IC of oxide coatings. To investigate lithologic influence on the results of sequential leaching, we selected two sites with complete bulk sediment statistical characterization. Site U1370 in the South Pacific Gyre, is predominantly composed of Rhyolite ( 60%) and has a distinguishable ( 10%) Fe-Mn Oxyhydroxide component (Dunlea et al., 2015). Site 1149 near the Izu-Bonin-Arc is predominantly composed of dispersed ash ( 20-50%) and eolian dust from Asia ( 50-80%) (Scudder et al., 2014). We perform a two-step leaching procedure: a 14 mL of 0.02 M hydroxylamine hydrochloride (HH) in 20% acetic acid buffered to a pH 4 for one hour, targeting metals bound to Fe- and Mn- oxides fractions, and a second HH leach for 12 hours, designed to remove any remaining oxides from the residual component. We analyze all three resulting fractions for a large suite of major, trace and rare earth elements, a sub-set of the samples are also analyzed for Nd IC. We use multivariate statistical analyses of the resulting geochemical data to identify how each component of the sediment partitions across the sequential

  10. Mantle xenoliths from Nemby, Eastern Paraguay: O-Sr-Nd isotopes and trace elements of hosted clinopyroxenes

    International Nuclear Information System (INIS)

    Comin-Chiaramonti, P; Antonini, P; Girardi, V.A.V; Gomes, C.B; Laurora, S; Zanetti, A

    2001-01-01

    depleted compositions, both in LK and HK suites. It is believed that 'residual' pyroxenes incorporated REE during later metasomatic events (cf. Chen et al., 1989). The above observation is consistent with the Nd isotope ratios measured on clinopyroxenes, indicating a LREE-depleted source for some samples and supporting the hypothesis that clinopyroxenes from some lherzolites did not crystallize from an original LREE enriched component; other samples approach enriched or undifferentiated compositions. Alkaline basaltic magmas from deeper, garnetbearing mantle may be suitable enrichment agents (cf. Comin-Chiaramonti et al, 1997). Moreover, the Nemby xenoliths were probably involved in carbonatite metasomatism (Comin-Chiaramonti et al., 1991), as possibly indicated by the IE patterns of some clinopyroxenes. The latter are characterized by high LREE and Sr abundances coupled with depletion in Nb, Ti, Zr. Notably, similar behaviour has already been described for clinopyroxenes from peridotite xenoliths hosted in ocean island basalts from Samoa and Tubai, which, according to Hauri et 2 al. (1993), show clear evidence of carbonatitic metasomatism.This suggests a buffering dominated by olivine in the upper mantle, where the equilibration is supported by coherence between observed Oisotope fractionation and clinopyroxene temperatures. The observed radiogenic isotope trend (Bulk Earth vs Depleted Mantle) is not consistent with major element refractory parameters. A mixing between depleted and enriched components is suggested by isotope records both in clinopyroxenes and on a whole-rock scale (Fig. 3A). The enriched components were mostly trapped in some clinopyroxenes, which had previously crystallized from depleted to quasi-chondritic mantle sources. On the whole, the isotopic data seem to indicate that the lithospheric mantle prior to the enrichment event(s) was dominated by a depleted component, isotopically resembling MORB sources (cf. Song and Frey, 1989; Comin-Chiaramonti et

  11. Towards isotope shift and hyperfine structure measurements of the element nobelium

    Energy Technology Data Exchange (ETDEWEB)

    Chhetri, Premaditya; Lautenschlaeger, Felix; Walther, Thomas [Institut fuer Angewandte Physik, TU Darmstadt, D-64289 Darmstadt (Germany); Laatiaoui, Mustapha [Helmholtz Institut Mainz, D-55099 Mainz (Germany); Block, Michael; Hessberger, Fritz-Peter [Helmholtz Institut Mainz, D-55099 Mainz (Germany); GSI, D-64291 Darmstadt (Germany); Lauth, Werner; Backe, Hartmut [Institut fuer Kernphysik, JGU Mainz, D-55122 Mainz (Germany); Kunz, Peter [TRIUMF, D-V6T2A3 Vancouver (Canada)

    2014-07-01

    Laser spectroscopy on the heaviest elements is of great interest as it allows the study of the evolution of relativistic effects on their atomic structure. In our experiment we exploit the Radiation Detected Resonance Ionization Spectroscopy technique and use excimer-laser pumped dye lasers to search for the first time the {sup 1}P{sub 1} level in {sup 254}No. Etalons will be used in the forthcoming experiments at GSI, Darmstadt, to narrow down the bandwidth of the dye lasers to 0.04 cm{sup -1}, for the determination of the isotope shift and hyperfine splitting of {sup 253,} {sup 255}No. In this talk results from preparatory hyperfine structure studies in nat. ytterbium and the perspectives for future experiments of the heaviest elements are discussed.

  12. Nd, Sr-isotopic provenance and trace element geochemistry of Amazonian foreland basin fluvial sands, Bolivia and Peru: Implications for ensialic Andean orogeny

    International Nuclear Information System (INIS)

    Basu, A.R.; Sharma, M.; DeCelles, P.G.

    1990-01-01

    Nd and Sr isotopes and the trace element contents, including the rare earths, were determined for fluvial sands of lithic arenite composition from the Madre de Dios foreland basin of Bolivia and Peru. On standard petrologic ternary diagrams, the sands fall in the recycled orogen provenance field and thus are similar to typical ancient foreland basin composition. The average rare earth elemental pattern of the sands is identical to the upper continental crustal average, as estimated from post-Archean composite shales of different continents. Ratio of Th/U, Co/Th, La/Sc and Th/Sc of the fluvial sands are intermediate between an average magmatic arc and an upper crustal average compositions. The dispersion of some trace elemental patterns in the sands can be attributed to fractionation of dense minerals, including zircon, during the sedimentation process. The variations of Nd isotopes in conjunction with the petrographic parameters of lithic metamorphic (Lm) and volcanic (Lv) fragments allow a two-fold classification of the sands. These two sand types can be interpreted in terms of mixing among three different provenances: one volcanic rock-suit with less negative ε Nd (O) parameter than the other volcanic suite, and a third metasedimentary source with ε Nd (O) value of around -12, which is considered to be similar to the average western Brazilian shield composition. Thus the overall compositions of the sands has been modeled as mechanical mixtures of two components, an Andean magmatic arc and the Brazilian shield-derived metasediments. The model is strongly supported by a plot of ε Nd (O) versus ε Sr (O) of the sands. In this plot, the Type 1 and 2 sands define two coherent hyperbolic trends contiguous with two different portions of the Andean magmatic trend. (orig./WB)

  13. Technical Report on the Behavior of Trace Elements, Stable Isotopes, and Radiogenic Isotopes During the Processing of Uranium Ore to Uranium Ore Concentrate

    Energy Technology Data Exchange (ETDEWEB)

    Marks, N. E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Borg, L. E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Eppich, G. R. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Gaffney, A. M. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Genneti, V. G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Hutcheon, I. D. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kristo, M. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Lindvall, R. E. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Ramon, C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Robel, M. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Roberts, S. K. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Schorzman, K. C. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Sharp, M. A. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Singleton, M. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Williams, R. W. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2015-07-09

    The goals of this SP-1 effort were to understand how isotopic and elemental signatures behave during mining, milling, and concentration and to identify analytes that might preserve geologic signatures of the protolith ores. The impurities that are preserved through the concentration process could provide useful forensic signatures and perhaps prove diagnostic of sample origin.

  14. The effect of phosphomonoesterases on the oxygen isotope composition of phosphate

    Science.gov (United States)

    von Sperber, Christian; Kries, Hajo; Tamburini, Federica; Bernasconi, Stefano M.; Frossard, Emmanuel

    2014-01-01

    Plants and microorganisms under phosphorus (P) stress release extracellular phosphatases as a strategy to acquire inorganic phosphate (Pi). These enzymes catalyze the hydrolysis of phosphoesters leading to a release of Pi. During the enzymatic hydrolysis an isotopic fractionation (ε) occurs leaving an imprint on the oxygen isotope composition of the released Pi which might be used to trace phosphorus in the environment. Therefore, enzymatic assays with acid phosphatases from wheat germ and potato tuber and alkaline phosphatase from Escherichia coli were prepared in order to determine the oxygen isotope fractionation caused by these enzymes. Adenosine 5‧ monophosphate and glycerol phosphate were used as substrates. The oxygen isotope fractionation caused by acid phosphatases is 20-30‰ smaller than for alkaline phosphatases, resulting in a difference of 5-7.5‰ in δ18O of Pi depending on the enzyme. We attribute the enzyme dependence of the isotopic fractionation to distinct reaction mechanisms of the two types of phosphatases. The observed difference is large enough to distinguish between the two enzymatic processes in environmental samples. These findings show that the oxygen isotope composition of Pi can be used to trace different enzymatic processes, offering an analytical tool that might contribute to a better understanding of the P-cycle in the environment.

  15. An isotope trace element study of the East Greenland Tertiary dyke swarm

    DEFF Research Database (Denmark)

    Hanghøj, Karen; Storey, Michael; Stecher, Ole

    2003-01-01

    Dykes of the East Greenland Tertiary dyke swarm can be divided into pre- and syn-break-up tholeiitic dykes, and post-break-up transitional dykes. Of the pre- and syn-break-up dykes, the most abundant group (Tholeiitic Series; TS) has major element compositions similar to the main part of the East...

  16. Source Attribution of Cyanides using Anionic Impurity Profiling, Stable Isotope Ratios, Trace Elemental Analysis and Chemometrics

    Energy Technology Data Exchange (ETDEWEB)

    Mirjankar, Nikhil S.; Fraga, Carlos G.; Carman, April J.; Moran, James J.

    2016-01-08

    Chemical attribution signatures (CAS) for chemical threat agents (CTAs) are being investigated to provide an evidentiary link between CTAs and specific sources to support criminal investigations and prosecutions. In a previous study, anionic impurity profiles developed using high performance ion chromatography (HPIC) were demonstrated as CAS for matching samples from eight potassium cyanide (KCN) stocks to their reported countries of origin. Herein, a larger number of solid KCN stocks (n = 13) and, for the first time, solid sodium cyanide (NaCN) stocks (n = 15) were examined to determine what additional sourcing information can be obtained through anion, carbon stable isotope, and elemental analyses of cyanide stocks by HPIC, isotope ratio mass spectrometry (IRMS), and inductively coupled plasma optical emission spectroscopy (ICP-OES), respectively. The HPIC anion data was evaluated using the variable selection methods of Fisher-ratio (F-ratio), interval partial least squares (iPLS), and genetic algorithm-based partial least squares (GAPLS) and the classification methods of partial least squares discriminate analysis (PLSDA), K nearest neighbors (KNN), and support vector machines discriminate analysis (SVMDA). In summary, hierarchical cluster analysis (HCA) of anion impurity profiles from multiple cyanide stocks from six reported country of origins resulted in cyanide samples clustering into three groups: Czech Republic, Germany, and United States, independent of the associated alkali metal (K or Na). The three country groups were independently corroborated by HCA of cyanide elemental profiles and corresponded to countries with known solid cyanide factories. Both the anion and elemental CAS are believed to originate from the aqueous alkali hydroxides used in cyanide manufacture. Carbon stable isotope measurements resulted in two clusters: Germany and United States (the single Czech stock grouped with United States stocks). The carbon isotope CAS is believed to

  17. Stable isotope composition and volume of Early Archaean oceans

    DEFF Research Database (Denmark)

    Pope, Emily Catherine; Rosing, Minik Thorleif; Bird, Dennis K.

    via biogenic methanogenesis [2]. Mass balance considerations within the Earth system places a cumulative upper limit on elemental hydrogen loss to space of ~1.8x1022mol elemental hydrogen H, constraining maximum Archaean atmospheric methane levels at ~3.8Ga to

  18. Memories of Earth Formation in the Modern Mantle: W Isotopic Composition of Flood Basalt Lavas

    Science.gov (United States)

    Rizo Garza, H. L.; Walker, R. J.; Carlson, R.; Horan, M. F.; Mukhopadhyay, S.; Francis, D.; Jackson, M. G.

    2015-12-01

    Four and a half billion years of geologic activity has overprinted much of the direct evidence for processes involved in Earth's formation and its initial chemical differentiation. Xenon isotopic ratios [1] and 3He/22Ne ratios [2] suggest that heterogeneities formed during Earth's accretion have been preserved to the present time. New opportunities to learn about early Earth history have opened up with the development of analytical techniques that allow high precision analysis of short-lived isotopic systems. The Hf-W system (t½ = 8.9 Ma) is particularly valuable for studying events that occurred during the first ~50 Ma of Solar System history. Here we report new data for ~ 60 Ma Baffin Bay and ~ 120 Ma Ontong Java Plateau lava samples. Both are large igneous provinces that may have sampled a primitive, less degassed deep mantle reservoir that has remained isolated since shortly after Earth formation [3,4]. Three samples analyzed have 182W/184W ratios that are 10 to 48 ppm higher than our terrestrial standard. These excesses in 182W are the highest ever measured in terrestrial rocks, and may reflect 182W ingrowth in an early-formed high Hf/W mantle domain that was produced by magma ocean differentiation [5]. Long and short-lived Sm-Nd systematics in these samples, however, are inconsistent with this hypothesis. The 182W excessses could rather reflect the derivation of these lavas from a mantle reservoir that was isolated from late accretionary additions [6]. The chondritic initial Os isotopic compositions and highly siderophile element abundances of these samples, however, are inconsistent with this interpretation. Tungsten concentrations for the Baffin Bay and Ontong Java Plateau samples range from 23 ppb to 62 ppb, and are negatively correlated with their 182W/184W ratios. We propose that the source reservoirs for these flood basalts likely formed through Hf/W fractionation caused by core-forming events occuring over a protacted time interval during Earth

  19. Search of the decay of the heaviest isotopes of element 112

    International Nuclear Information System (INIS)

    Oganesyan, Yu.Ts.; Eremin, A.V.; Gul'bekyan, G.G.

    1998-01-01

    To produce heavy isotopes of element 112 in the reaction 48 Ca + 238 U two experiments at different beam energies were performed. In the first experiment the beam energy at the middle of the target was 231 MeV which leads to the production of the compound nucleus 286 112 with an excitation energy of E x = 33 MeV. In a 20 - day irradiation of the 238 U target with a beam dose of 3.5 x 10 18 on the focal plane of the recoil separator VASSILISSA two spontaneous fission events were detected. No α-particle emission preceding spontaneous fission nor α-α correlation in the energy range from 8 to 13 MeV in the time interval of up to 10000 s. have been observed. The most probable explanation of the data obtained in this experiment is that the observed spontaneous fission corresponds to the decay of the even-odd isotope (N = 171) of element 112 produced in the reaction 238 U ( 48 Ca, 3n) 283 112 with a cross section of ∼ 5 pb. The half-life of the new spontaneous fission nuclide is about 100 s. In the second experiment the beam energy was 238 MeV which increases the excitation energy of compound nuclei up to E x = 39 MeV. The total beam dose in that case was 2.2 x 10 18 . No events due either to spontaneous fission or sequential α-α decay in an energy range from 8 to 12 MeV and the time interval of 1000 s. were detected. These data give the upper limit of 3 pb for the production cross section of the even-even isotope 282 112 in the reaction 238 U ( 48 Ca, 4n) 282 112

  20. Trace element and isotopic effects arising from magma migration beneath mid-ocean ridges

    International Nuclear Information System (INIS)

    Kenyon, P.M.

    1990-01-01

    The trace element concentrations and isotopic ratios in the magma erupted on mid-ocean ridges may differ from those in the source material due to physical effects such as porous flow dispersion, exchange of trace elements between the fluid and solid phases during magma migration, and convective mixing in magma chambers. These differences are in addition to those produced by better known processes such as fractional crystallization and partial melting. The effects of the three former processes are described. It is predicted that magma typically reaches the sub-ridge magma chambers with a spatial heterogeneity only slightly reduced from that of the source material, but with a subdued variation in time. Convective mixing then further reduces the spatial heterogeneity. Application of the results for convective mixing to a recent Fourier analysis of 87 Sr/ 86 Sr variations along the Mid-Atlantic Ridge suggests that the falloff in amplitude of variation observed with decreasing wavelength in the Mid-Atlantic Ridge data cannot be explained by convective mixing in magma chambers. Instead, it is postulated that this falloff is due to the mechanics of the production and/or the solid-state convective mixing of chemical and isotopic heterogeneities in the solid mantle. (orig.)

  1. Unexpected variations in the triple oxygen isotope composition of stratospheric carbon dioxide

    Science.gov (United States)

    Wiegel, Aaron A.; Cole, Amanda S.; Hoag, Katherine J.; Atlas, Elliot L.; Schauffler, Sue M.; Boering, Kristie A.

    2013-10-01

    We report observations of stratospheric CO2 that reveal surprisingly large anomalous enrichments in 17O that vary systematically with latitude, altitude, and season. The triple isotope slopes reached 1.95 ± 0.05(1σ) in the middle stratosphere and 2.22 ± 0.07 in the Arctic vortex versus 1.71 ± 0.03 from previous observations and a remarkable factor of 4 larger than the mass-dependent value of 0.52. Kinetics modeling of laboratory measurements of photochemical ozone-CO2 isotope exchange demonstrates that non-mass-dependent isotope effects in ozone formation alone quantitatively account for the 17O anomaly in CO2 in the laboratory, resolving long-standing discrepancies between models and laboratory measurements. Model sensitivities to hypothetical mass-dependent isotope effects in reactions involving O3, O(1D), or CO2 and to an empirically derived temperature dependence of the anomalous kinetic isotope effects in ozone formation then provide a conceptual framework for understanding the differences in the isotopic composition and the triple isotope slopes between the laboratory and the stratosphere and between different regions of the stratosphere. This understanding in turn provides a firmer foundation for the diverse biogeochemical and paleoclimate applications of 17O anomalies in tropospheric CO2, O2, mineral sulfates, and fossil bones and teeth, which all derive from stratospheric CO2.

  2. Impact on the environment from steel bridge paint deterioration using lead isotopic tracing, paint compositions and soil deconstruction

    Energy Technology Data Exchange (ETDEWEB)

    Gulson, Brian, E-mail: brian.gulson@mq.edu.au [Department of Environmental Science, Macquarie University, Sydney, NSW 2109 (Australia); CSIRO Energy Flagship, North Ryde, NSW 2113 (Australia); Chiaradia, Massimo [Department of Mineralogy, University of Geneva, Geneva (Switzerland); Davis, Jeffrey [CSIRO Energy Flagship, North Ryde, NSW 2113 (Australia); O' Connor, Gary [Queensland Department of Environment & Heritage Protection, Brisbane, QLD 4000 (Australia)

    2016-04-15

    Deterioration and repair of lead paint on steel structures can result in contamination of the ambient environment but other sources of lead such as from past use of leaded paint and gasoline and industrial activities can also contribute to the contamination. Using a combination of high precision lead isotopic tracing, detailed paint examination, including with scanning electron microscopy, and soil deconstruction we have compared paint on a steel bridge and bulk soil and lead-rich particles separated from soil. The majority of Pb found in the paint derives from Australian sources but some also has a probable US origin. The isotopic data for the bulk soils and selected particles lie on a mixing line with end members the geologically ancient Broken Hill lead and possible European lead which is suggested to be derived from old lead paint and industrial activities. Data for gasoline-derived particulates lie on this array and probably contribute to soil Pb. Although paint from the bridge can be a source of lead in the soils, isotopic tracing, paint morphology and mineralogical identification indicate that other sources, including from paint, gasoline and industrial activities, are contributing factors to the lead burden. Even though physical characteristics and elemental composition are the same in some particles, the isotopic signatures demonstrate that the sources are different. Plots using {sup 206}Pb/{sup 208}Pb vs {sup 206}Pb/{sup 207}Pb ratios, the common representation these days, do not allow for source discrimination in this investigation. - Highlights: • Soil Pb values up to 1200 mg/kg below Pb painted bridge • Microscopy & SEM characterised up to 6 different paint layers. • Isotopes identified different sources of Pb including paint and gasoline. • Multiple methods provide definitive answers.

  3. Multivariate statistical analysis of the hydrogeochemical and isotopic composition of the groundwater resources in northeastern Peloponnesus (Greece).

    Science.gov (United States)

    Matiatos, Ioannis; Alexopoulos, Apostolos; Godelitsas, Athanasios

    2014-04-01

    The present study involves an integration of the hydrogeological, hydrochemical and isotopic (both stable and radiogenic) data of the groundwater samples taken from aquifers occurring in the region of northeastern Peloponnesus. Special emphasis has been given to health-related ions and isotopes in relation to the WHO and USEPA guidelines, to highlight the concentrations of compounds (e.g., As and Ba) exceeding the drinking water thresholds. Multivariate statistical analyses, i.e. two principal component analyses (PCA) and one discriminant analysis (DA), combined with conventional hydrochemical methodologies, were applied, with the aim to interpret the spatial variations in the groundwater quality and to identify the main hydrogeochemical factors and human activities responsible for the high ion concentrations and isotopic content in the groundwater analysed. The first PCA resulted in a three component model, which explained approximately 82% of the total variance of the data sets and enabled the identification of the hydrogeological processes responsible for the isotopic content i.e., δ(18)Ο, tritium and (222)Rn. The second PCA, involving the trace element presence in the water samples, revealed a four component model, which explained approximately 89% of the total variance of the data sets, giving more insight into the geochemical and anthropogenic controls on the groundwater composition (e.g., water-rock interaction, hydrothermal activity and agricultural activities). Using discriminant analysis, a four parameter (δ(18)O, (Ca+Mg)/(HCO3+SO4), EC and Cl) discriminant function concerning the (222)Rn content was derived, which favoured a classification of the samples according to the concentration of (222)Rn as (222)Rn-safe (11 Bq·L(-1)). The selection of radon builds on the fact that this radiogenic isotope has been generally related to increased health risk when consumed. Copyright © 2014 Elsevier B.V. All rights reserved.

  4. Variable sulfur isotope composition of sulfides provide evidence for multiple sources of contamination in the Rustenburg Layered Suite, Bushveld Complex

    Science.gov (United States)

    Magalhães, Nivea; Penniston-Dorland, Sarah; Farquhar, James; Mathez, Edmond A.

    2018-06-01

    The Rustenburg Layered Suite (RLS) of the Bushveld Complex (BC) is famous for its platinum group element (PGE) ore, which is hosted in sulfides. The source of sulfur necessary to generate this type of mineralization is inferred to be the host rock of the intrusion. The RLS has a sulfur isotopic signature that indicates the presence of Archean surface-derived material (Δ33 S ≠ 0) in the magma. This signature, with an average value of Δ33 S = 0.112 ± 0.024 ‰, deviates from the expected Δ33 S value of the mantle of 0 ± 0.008 ‰. Previous work suggested that this signature is uniform throughout the RLS, which contrasts with radiogenic isotopes which vary throughout the igneous stratigraphy of the RLS. In this study, samples from key intervals within the igneous stratigraphy were analyzed, showing that Δ33 S values vary in the same stratigraphic levels as Sr and Nd isotopes. However, the variation is not consistent; in some levels there is a positive correlation and in others a negative correlation. This observation suggests that in some cases distinct magma pulses contained assimilated sulfur from different sources. Textural analysis shows no evidence for late addition of sulfur. These results also suggest that it is unlikely that large-scale assimilation and/or efficient mixing of host rock material in a single magma chamber occurred during emplacement. The data do not uniquely identify the source of sulfur in the different layers of the RLS, but the variation in sulfur isotope composition and its relationship to radiogenic isotope data calls for a reevaluation of the models for the formation and evolution of the RLS, which has the potential to impact the knowledge of how PGE deposits form.

  5. Determining the isotopic compositions of uranium and fission products in radioactive environmental microsamples using laser ablation ICP-MS with multiple ion counters

    International Nuclear Information System (INIS)

    Boulyga, Sergei F.; Prohaska, Thomas

    2008-01-01

    This paper presents the application of a multicollector inductively coupled plasma mass spectrometer (MC-ICP-MS) - a Nu Plasma HR - equipped with three ion-counting multipliers and coupled to a laser ablation system (LA) for the rapid and sensitive determination of the 235 U/ 238 U, 236 U/ 238 U, 145 Nd/ 143 Nd, 146 Nd/ 143 Nd, 101 Ru/( 99 Ru+ 99 Tc) and 102 Ru/( 99 Ru+ 99 Tc) isotope ratios in microsamples collected in the vicinity of Chernobyl. Microsamples with dimensions ranging from a hundred μm to about 1 mm and with surface alpha activities of 3-38 mBq were first identified using nuclear track radiography. U, Nd and Ru isotope systems were then measured sequentially for the same microsample by LA-MC-ICP-MS. The application of a zoom ion optic for aligning the ion beams into the ion counters allows fast switching between different isotope systems, which enables all of the abovementioned isotope ratios to be measured for the same microsample within a total analysis time of 15-20 min (excluding MC-ICP-MS optimization and calibration). The 101 Ru/( 99 Ru+ 99 Tc) and 102 Ru/( 99 Ru+ 99 Tc) isotope ratios were measured for four microsamples and were found to be significantly lower than the natural ratios, indicating that the microsamples were contaminated with the corresponding fission products (Ru and Tc). A slight depletion in 146 Nd of about 3-5% was observed in the contaminated samples, but the Nd isotopic ratios measured in the contaminated samples coincided with natural isotopic composition within the measurement uncertainty, as most of the Nd in the analyzed samples originates from the natural soil load of this element. The 235 U/ 238 U and 236 U/ 238 U isotope ratios were the most sensitive indicators of irradiated uranium. The present work yielded a significant variation in uranium isotope ratios in microsamples, in contrast with previously published results from the bulk analysis of contaminated samples originating from the vicinity of Chernobyl. Thus

  6. Determining the isotopic compositions of uranium and fission products in radioactive environmental microsamples using laser ablation ICP-MS with multiple ion counters.

    Science.gov (United States)

    Boulyga, Sergei F; Prohaska, Thomas

    2008-01-01

    This paper presents the application of a multicollector inductively coupled plasma mass spectrometer (MC-ICP-MS)--a Nu Plasma HR--equipped with three ion-counting multipliers and coupled to a laser ablation system (LA) for the rapid and sensitive determination of the 235U/238U, 236U/238U, 145Nd/143Nd, 146Nd/143Nd, 101Ru/(99Ru+99Tc) and 102Ru/(99Ru+99Tc) isotope ratios in microsamples collected in the vicinity of Chernobyl. Microsamples with dimensions ranging from a hundred mum to about 1 mm and with surface alpha activities of 3-38 mBq were first identified using nuclear track radiography. U, Nd and Ru isotope systems were then measured sequentially for the same microsample by LA-MC-ICP-MS. The application of a zoom ion optic for aligning the ion beams into the ion counters allows fast switching between different isotope systems, which enables all of the abovementioned isotope ratios to be measured for the same microsample within a total analysis time of 15-20 min (excluding MC-ICP-MS optimization and calibration). The 101Ru/(99Ru+99Tc) and 102Ru/(99Ru+99Tc) isotope ratios were measured for four microsamples and were found to be significantly lower than the natural ratios, indicating that the microsamples were contaminated with the corresponding fission products (Ru and Tc). A slight depletion in 146Nd of about 3-5% was observed in the contaminated samples, but the Nd isotopic ratios measured in the contaminated samples coincided with natural isotopic composition within the measurement uncertainty, as most of the Nd in the analyzed samples originates from the natural soil load of this element. The 235U/238U and 236U/238U isotope ratios were the most sensitive indicators of irradiated uranium. The present work yielded a significant variation in uranium isotope ratios in microsamples, in contrast with previously published results from the bulk analysis of contaminated samples originating from the vicinity of Chernobyl. Thus, the 235U/238U ratios measured in ten

  7. The isotopic composition of precipitation on the Andes and Amazon of Bolivia

    International Nuclear Information System (INIS)

    Roche, M.A.; Gonfiantini, R.; Fontes, J.C.; Abasto, N.; Noriega, L.

    1999-01-01

    In the years 1983-1985, the isotopic composition of precipitation was determined in monthly and annual samples collected from stations at different altitude along two transects from the Bolivian Altiplano to the Amazon basin. The data show variations with amount (in rainy season δ-values are more negative) and altitude. The isotopic gradient with altitude changes seasonally, being higher (in absolute value) in rainy months (January-February). The influence of the 1983 drought is clearly shown, with less negative δ-values and smaller isotopic gradients vs. altitude with respect to 1984. The drought was supposed to be connected with El Nino, very strong in 1982-1983, but this has not been confirmed in 1997-1998, when El Nino was even stronger. The isotopic contrast between the dry 1983 and the very humid 1984 can be identified in the ice core from the Sahama glacier. (author)

  8. Modelling the regional climate and isotopic composition of Svalbard precipitation using REMOiso

    DEFF Research Database (Denmark)

    Divine..[], D.V.; Sjolte, Jesper; Isaksson, E.

    2011-01-01

    Simulations of a regional (approx. 50 km resolution) circulation model REMOiso with embedded stable water isotope module covering the period 1958-2001 are compared with the two instrumental climate and four isotope series (d18O) from western Svalbard. We examine the data from ice cores drilled...... than summer. The simulated and measured Holtedahlfonna d18O series agree reasonably well, whereas no significant correlation has been observed between the modelled and measured Lomonosovfonna ice core isotopic series. It is shown that sporadic nature as well as variability in the amount inherent...... in reproducing the local climate. The model successfully captures the climate variations on the daily to multidecadal times scales although it tends to systematically underestimate the winter SAT. Analysis suggests that REMOiso performs better at simulating isotope compositions of precipitation in the winter...

  9. Isotopic composition of groundwater in semi-arid regions of Southern Africa

    International Nuclear Information System (INIS)

    Vogel, J.C.; Urk, H. van

    1975-01-01

    Although the isotope content of precipitation in the semi-arid regions of southern Africa is extremely variable, groundwater samples from the same district are found to have a remarkably constant isotopic composition. The oxygen-18 content of the underground water, in general, varies by about 0.5% in a given area. The differences that occur between different regions are sufficiently large to allow the groundwater of an area to be characterized by means of its oxygen-18 content. In order to localize the infiltration area of an aquifer, radiocarbon dating of the water is used. It appears that the groundwater contains, in general, less of the heavy isotopes than does the precipitation in the recharge area. This indicates that infiltration only takes place during periods of heavy rainfall. Examples are given where the isotope content of the groundwater is used to distinguish between different aquifers in the same region

  10. Stable isotope compositions (O-C) of reef fish otoliths from the Taiaro lagoon (Tuamotu, French Polynesia): isotopic and biologic implications

    International Nuclear Information System (INIS)

    Blamart, D.; Juillet-Leclerc, A.; Ouahdi, R.; Escoubeyrou, K.; Lecomte-Finiger, R.

    2002-01-01

    Nuclei (larval stage) and outer parts (adult stage) of fish otoliths from the Taiaro closed lagoon (French Polynesia) and adjacent ocean have been analysed for the C-O isotopic compositions. δ 18 O values of the nuclei of both populations indicate that isotopic equilibrium is reached. This implies that the lagoonal fish population has done its complete biological cycle in the lagoon and represents an adaptation in a closed system. δ 18 O values of the outer parts show a slight isotopic disequilibrium ( 13 C values exhibit a strong isotopic disequilibrium related to metabolic activity. (authors)

  11. Lead contamination and transfer in urban environmental compartments analyzed by lead levels and isotopic compositions.

    Science.gov (United States)

    Hu, Xin; Sun, Yuanyuan; Ding, Zhuhong; Zhang, Yun; Wu, Jichun; Lian, Hongzhen; Wang, Tijian

    2014-04-01

    Lead levels and isotopic compositions in atmospheric particles (TSP and PM2.5), street dust and surface soil collected from Nanjing, a mega city in China, were analyzed to investigate the contamination and the transfer of lead in urban environmental compartments. The lead contents in TSP and PM2.5 are significantly higher than them in the surface soil and street dust (p lead to the major crustal elements (Al, Sr, Ti and Fe) indicates significant lead enrichment in atmospheric particles. The plots of (206)Pb/(207)Pb vs.(208)Pb/(206)Pb and (206)Pb/(207)Pb vs. 1/Pb imply that the street dust and atmospheric particles (TSP and PM2.5) have very similar lead sources. Coal emissions and smelting activities may be the important lead sources for street dust and atmospheric particles (TSP and PM2.5), while the deposition of airborne lead is an important lead source for urban surface soil. Copyright © 2013 Elsevier Ltd. All rights reserved.

  12. Oxygen and carbon isotopic compositions of gases respired by humans

    International Nuclear Information System (INIS)

    Epstein, S.; Zeiri, L.

    1988-01-01

    Oxygen-isotope fractionation associated with respiration in human individuals at rest is linearly related to the fraction of the O 2 utilized in the respiration process. The slope of this relationship is affected by a history of smoking, by vigorous exercise, and by the N 2 /O 2 ratio of the inhaled gas. For patients who suffer anemia-related diseases, the slope of this relationship is directly proportional to their level of hemoglobin. These results introduce a new approach for studying the mechanisms of O 2 consumption in human respiration and how they are affected by related diseases

  13. [Changes of chlorine isotope composition characterize bacterial dehalogenation of dichloromethane].

    Science.gov (United States)

    Ziakun, A M; Firsova, Iu E; Torgonskaia, M L; Doronina, N V; Trotsenko, Iu A

    2007-01-01

    Fractionation of dichloromethane (DCM) molecules with different chlorine isotopes by aerobic methylobacteria Methylobacterium dichloromethanicum DM4 and Albibacter nethylovorans DM10; cell-free extract of strain DM4; and transconjugant Methylobacterium evtorquens Al1/pME 8220, expressing the dcmA gene for DCM dehalogenase but unable to grow on DCM, was studied. Kinetic indices of DCM isotopomers for chlorine during bacterial dehalogenation and diffusion were compared. A two-step model is proposed, which suggests diffusional DCM transport to bacterial cells.

  14. Improved accuracy and precision in δ15 NAIR measurements of explosives, urea, and inorganic nitrates by elemental analyzer/isotope ratio mass spectrometry using thermal decomposition.

    Science.gov (United States)

    Lott, Michael J; Howa, John D; Chesson, Lesley A; Ehleringer, James R

    2015-08-15

    Elemental analyzer systems generate N(2) and CO(2) for elemental composition and isotope ratio measurements. As quantitative conversion of nitrogen in some materials (i.e., nitrate salts and nitro-organic compounds) is difficult, this study tests a recently published method - thermal decomposition without the addition of O(2) - for the analysis of these materials. Elemental analyzer/isotope ratio mass spectrometry (EA/IRMS) was used to compare the traditional combustion method (CM) and the thermal decomposition method (TDM), where additional O(2) is eliminated from the reaction. The comparisons used organic and inorganic materials with oxidized and/or reduced nitrogen and included ureas, nitrate salts, ammonium sulfate, nitro esters, and nitramines. Previous TDM applications were limited to nitrate salts and ammonium sulfate. The measurement precision and accuracy were compared to determine the effectiveness of converting materials containing different fractions of oxidized nitrogen into N(2). The δ(13) C(VPDB) values were not meaningfully different when measured via CM or TDM, allowing for the analysis of multiple elements in one sample. For materials containing oxidized nitrogen, (15) N measurements made using thermal decomposition were more precise than those made using combustion. The precision was similar between the methods for materials containing reduced nitrogen. The %N values were closer to theoretical when measured by TDM than by CM. The δ(15) N(AIR) values of purchased nitrate salts and ureas were nearer to the known values when analyzed using thermal decomposition than using combustion. The thermal decomposition method addresses insufficient recovery of nitrogen during elemental analysis in a variety of organic and inorganic materials. Its implementation requires relatively few changes to the elemental analyzer. Using TDM, it is possible to directly calibrate certain organic materials to international nitrate isotope reference materials without off

  15. Trace and minor element variations and sulfur isotopes in crystalline and colloform ZnS: Incorporation mechanisms and implications for their genesis

    Science.gov (United States)

    Pfaff, Katharina; Koenig, Alan; Wenzel, Thomas; Ridley, Ian; Hildebrandt, Ludwig H.; Leach, David L.; Markl, Gregor

    2011-01-01

    Various models have been proposed to explain the formation mechanism of colloform sphalerite, but the origin is still under debate. In order to decipher influences on trace element incorporation and sulfur isotope composition, crystalline and colloform sphalerite from the carbonate-hosted Mississippi-Valley Type (MVT) deposit near Wiesloch, SW Germany, were investigated and compared to sphalerite samples from 52 hydrothermal vein-type deposits in the Schwarzwald ore district, SW Germany to study the influence of different host rocks, formation mechanisms and fluid origin on trace element incorporation. Trace and minor element incorporation in sphalerite shows some correlation to their host rock and/or origin of fluid, gangue, paragenetic minerals and precipitation mechanisms (e.g., diagenetic processes, fluid cooling or fluid mixing). Furthermore, crystalline sphalerite is generally enriched in elements like Cd, Cu, Sb and Ag compared to colloform sphalerite that mainly incorporates elements like As, Pb and Tl. In addition, sulfur isotopes are characterized by positive values for crystalline and strongly negative values for colloform sphalerite. The combination of trace element contents, typical minerals associated with colloform sphalerite from Wiesloch, sulfur isotopes and thermodynamic considerations helped to evaluate the involvement of sulfate-reducing bacteria in water-filled karst cavities. Sulfate-reducing bacteria cause a sulfide-rich environment that leads in case of a metal-rich fluid supply to a sudden oversaturation of the fluid with respect to galena, sphalerite and pyrite. This, however, exactly coincides with the observed crystallization sequence of samples involving colloform sphalerite from the Wiesloch MVT deposit.

  16. Silicon isotope fractionation by marine sponges and the reconstruction of the silicon isotope composition of ancient deep water

    Science.gov (United States)

    de La Rocha, Christina L.

    2003-05-01

    The silicon isotope composition (δ30Si) of biogenic opal provides a view of the silica cycle at times in the past. Reconstructions require the knowledge of silicon isotope fractionation during opal biomineralization. The δ30Si of specimens of hexactinellid sponges and demosponges growing in the modern ocean ranged from -1.2‰ to -3.7‰ (n = 6), corresponding to the production of opal that has a δ30Si value 3.8‰ ± 0.8‰ more negative than seawater silicic acid and a fractionation factor (α) of 0.9964. This is three times the fractionation observed during opal formation by marine diatoms and terrestrial plants and is the largest fractionation of silicon isotopes observed for any natural process on Earth. The δ30Si values of sponge spicules across the Eocene-Oligocene boundary at Ocean Drilling Program Site 689 on Maud Rise range from -1.1‰ to -3.0‰, overlapping the range observed for sponges growing in modern seawater.

  17. The study of the elemental composition of peppermint (Mentha piperita

    Directory of Open Access Journals (Sweden)

    K. V. Andrianov

    2014-12-01

    Full Text Available Introduction Our attention was drawn by quite widespread plant, namely peppermint (Mentha piperita of mint family (Lamiaceae L.. It isn’t known as a wild-growing plant, this plant is the hybrid received from crossing water mint (Mentha aquatica with a spicate mint (Mentha spicata or green mint (Mentha viridis. Therapeutic action of plant is caused by the BAS complex, among which essential oil, alkaloids, saponins, organic acids, vitamins, macro - and microelements are. Accumulation of elements in a plant directly depends on sort and species of this plant, climatic conditions and geographical places of growth. Thus, using pharmacognosic research of peppermint, it would be expedient to carry out the comparative analysis of the elements content in leaf of widespread species of this plant, and also to compare to element structure of peppermint from other region of preparation. Studying qualitative structure and quantitative content of macro - and microelements in leaf of 3 samples of peppermint became the purpose of our research. Materials and methods of research The peppermint leaves of 3 samples were the object of our research. They are ‘Chornolistaya’ sort – the sample #1, ‘Zgadka’ sort – the sample #2 (the stocking up place is Dnepropetrovsk region, 2013 and peppermint - the sample #3 (the stocking place is Lebanon, Baalbek surroundings, 2013. In order to study elemental structure of peppermint leaves, atomic emission spectrometry with photographic registration was used. Results and discussions All types of raw materials had identical element structure. According to the content in each type of raw materials, compositions can be divided into some groups: the first one – the content of element was near or above 1000 mg /100 g, the content was higher than 100 mg /100 g, the content of composition was lower than 100 mg /100 g and below than 1 mg /100 g. Thus, the ambit between these groups was deeply emphasized. The following

  18. Isotopic composition of water in precipitation in a region or place

    International Nuclear Information System (INIS)

    Singh, B.P.

    2013-01-01

    Stable isotopes of water molecules in hydrology, the water cycle and Craig's global meteoric water line (GMWL) relating δ 18 O and δ 2 H are well established with a slope of around 8 and an intercept of around 10. However, in many situations the slope is less than 8 and the intercept is smaller or even negative. These observations need to be understood and a method is suggested to correlate with the global meteoric water line (GMWL). How to find the isotopic composition of water at a particular place is also suggested. - Highlights: ► A best fit line is drawn between slopes of plots on δ 18 O and δ 2 H line versus intercept of the measurement in a region. ► A new approach is suggested to understand this experimental best fit line. ► The new method is suggested to achieve the isotopic composition of meteoric water in region or a place

  19. Comparison of different methods of determining plutonium content and isotopic composition

    International Nuclear Information System (INIS)

    Dowell, M.R.W.

    1985-05-01

    At Rockwell Hanford Operations, several different methods are used to determine plutonium content and isotopic composition. These include alpha particle energy analysis, calorimetry/gamma-ray analysis, mass spectrometry, and low energy ray assay. Each is used in a process control environment and has its advantages and disadvantages in terms of sample matrix, sample preparation, concentration, error ranges, detection limits, and turn around time. Of the methods discussed, special attention is paid to the Plutonium Isotopics Solution Counter, a low energy gamma ray assay system designed to provide plutonium and americium content and isotopic composition of Pu-238 through Pu-241 and Am-241. It is qualitatively and quantitatively compared to the other methods. A brief description of sample types which the Solution Counter analyzes is presented. 4 refs., 4 tabs

  20. Comparison of different methods of determining plutonium content and isotopic composition

    International Nuclear Information System (INIS)

    Anon.

    1986-01-01

    At Rockwell Hanford Operations, several different methods are used to determine plutonium content and isotopic composition. These include alpha particle energy analysis, calorimetry/gamma-ray analysis, mass spectrometry, and low energy gamma-ray assay. Each is used in a process control environment and has its advantages and disadvantages in terms of sample matrix, sample preparation, concentration, error ranges, detection limits, and turn around time. Of the methods discussed, special attention is paid to the Plutonium Isotopics Solution Counter, a low energy gamma-ray assay system designed to provide plutonium and americium content and isotopic composition of Pu-238 through Pu-241 and Am-241. It is qualitatively and quantitatively compared to the other methods. A brief description of sample types which the Solution Counter analyzes is presented

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

    Science.gov (United States)

    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

  2. The isotopic composition of methane in polar ice cores

    Science.gov (United States)

    Craig, H.; Chou, C. C.; Welhan, J. A.; Stevens, C. M.; Engelkemeir, A.

    1988-01-01

    Air bubbles in polar ice cores indicate that about 300 years ago the atmospheric mixing ratio of methane began to increase rapidly. Today the mixing ratio is about 1.7 parts per million by volume, and, having doubled once in the past several hundred years, it will double again in the next 60 years if current rates continue. Carbon isotope ratios in methane up to 350 years in age have been measured with as little as 25 kilograms of polar ice recovered in 4-meter-long ice-core segments. The data show that: (1) in situ microbiology or chemistry has not altered the ice-core methane concentrations, and (2) that the carbon-13 to carbon-12 ratio of atmospheric CH4 in ice from 100 years and 300 years ago was about 2 per mil lower than at present. Atmospheric methane has a rich spectrum of isotopic sources: the ice-core data indicate that anthropogenic burning of the earth's biomass is the principal cause of the recent C-13H4 enrichment, although other factors may also contribute.

  3. Subduction-like fluids in the genesis of Mt. Etna magmas: evidence from boron isotopes and fluid mobile elements

    Science.gov (United States)

    Tonarini, Sonia; Armienti, Pietro; D'Orazio, Massimo; Innocenti, Fabrizio

    2001-11-01

    New whole-rock B, Sr, Nd isotope ratios and 87Sr/ 86Sr on clinopyroxenes have been collected to study the enrichment of fluid mobile elements (FMEs) observed in Mt. Etna volcanics. Etna volcano, one of the most active in the world, is located in an extremely complex tectonic context at the boundary between colliding African and European plates. The analytical work focuses on current (1974-1998) and historic (1851-1971) eruptive activity, including some key prehistoric lavas, in order to interpret the secular shift of its geochemical signature to more alkaline compositions. Boron is used as a tool to unravel the role of fluids in the genesis of magmas, revealing far-reaching consequences, beyond the case study of Mt. Etna. Small variations are observed in δ 11B (-3.5 to -8.0‰), 87Sr/ 86Sr (0.70323-0.70370), and 143Nd/ 144Nd (0.51293-0.51287). Moreover, temporal evolution to higher δ 11B and 87Sr/ 86Sr, and to lower 143Nd/ 144Nd, is observed in the current activity, defining a regular trend. Sr isotopic equilibrium between whole-rock and clinopyroxene pairs indicates the successive introduction of three distinct magma types into the Etna plumbing system over time; these are characterized by differing degrees of FME enrichment. In addition, certain lavas exhibit evidence for country rock assimilation, magma-fluid interaction, or magma mixing in the shallow feeding system; at times these processes apparently lowered magmatic δ 11B and/or induced Sr isotopic disequilibrium between whole rock and clinopyroxene. The regular increase of δ 11B values is correlated with Nb/FME and 87Sr/ 86Sr ratios; these correlations are consistent with simple mixing between the mantle source and aqueous fluids derived from nearby Ionian slab. The best fit of Mt. Etna data is obtained using an enriched-MORB mantle source and a fluid phase with δ 11B of about -2‰ and 87Sr/ 86Sr of 0.708. We argue that the slab window generated by differential roll-back of subducting Ionian

  4. Temperature evolution and the oxygen isotope composition of Phanerozoic oceans from carbonate clumped isotope thermometry

    Science.gov (United States)

    Henkes, Gregory A.; Passey, Benjamin H.; Grossman, Ethan L.; Shenton, Brock J.; Yancey, Thomas E.; Pérez-Huerta, Alberto

    2018-05-01

    Surface temperature is among the most important parameters describing planetary climate and habitability, and yet there remains considerable debate about the temperature evolution of the Earth's oceans during the Phanerozoic Eon (541 million years ago to present), the time during which complex metazoan life radiated on Earth. Here we critically assess the emerging record of Phanerozoic ocean temperatures based on carbonate clumped isotope thermometry of fossil brachiopod and mollusk shells, and we present new data that fill important gaps in the Late Paleozoic record. We evaluate and reject the hypothesis that solid-state reordering of 13C-18O bonds has destroyed the primary clumped isotope temperature signal of most fossils during sedimentary burial at elevated temperatures. The resulting Phanerozoic record, which shows a general coupling between tropical seawater temperatures and atmospheric carbon dioxide (CO2) levels since the Paleozoic, indicates that tropical temperatures during the icehouse climate of the Carboniferous period were broadly similar to present (∼25-30 °C), and suggests that benthic metazoans were able to thrive at temperatures of 35-40 °C during intervals of the early and possibly the latest Paleozoic when CO2 levels were likely 5-10× higher than present-day values. Equally important, there is no resolvable trend in seawater oxygen isotope ratios (δ18 O) over the past ∼500 million years, indicating that the average temperature of oxygen exchange between seawater and the oceanic crust has been high (∼270 °C) since at least the early Paleozoic, which points to mid-ocean ridges as the dominant locus of water-rock interaction over the past half-billion years.

  5. Half-lives of long-lived isotopes of transactinium elements from 228Th to 257Fm

    International Nuclear Information System (INIS)

    Surin, V.M.; Fomushkin, Eh.F.

    1983-09-01

    The experimental measurements and critical evaluation results of the long-lived isotope half-decay periods of transactinium elements (from 228 Th to 257 Fm) are given on July 1981 to be published in open literature and related to the natural radioactive decay. From the massif of the known half-decay periods the most reliable data were selected, received or evaluated and recommended for practical use; the calculations of isotope specific activities were performed on this data. (author)

  6. Cl and C isotope analysis to assess the effectiveness of chlorinated ethene degradation by zero-valent iron: Evidence from dual element and product isotope values

    International Nuclear Information System (INIS)

    Audí-Miró, Carme; Cretnik, Stefan; Otero, Neus; Palau, Jordi; Shouakar-Stash, Orfan; Soler, Albert

    2013-01-01

    Highlights: ► TCE and cis-DCE Cl isotope fractionation was investigated for the first time with ZVI. ► A C–Cl bond is broken in the rate-limiting step during ethylene ZVI dechlorination. ► Dual C/Cl isotope plot is a promising tool to discriminate abiotic degradation. ► Product-related carbon isotopic fractionation gives evidence of abiotic degradation. ► Hydrogenolysis and β-dichloroelimination pathways occur simultaneously. - Abstract: This study investigated C and, for the first time, Cl isotope fractionation of trichloroethene (TCE) and cis-dichloroethene (cis-DCE) during reductive dechlorination by cast zero-valent iron (ZVI). Hydrogenolysis and β-dichloroelimination pathways occurred as parallel reactions, with ethene and ethane deriving from the β-dichloroelimination pathway. Carbon isotope fractionation of TCE and cis-DCE was consistent for different batches of Fe studied. Transformation of TCE and cis-DCE showed Cl isotopic enrichment factors (ε Cl ) of −2.6‰ ± 0.1‰ (TCE) and −6.2‰ ± 0.8‰ (cis-DCE), with Apparent Kinetic Isotope Effects (AKIE Cl ) for Cl of 1.008 ± 0.001 (TCE) and 1.013 ± 0.002 (cis-DCE). This indicates that a C–Cl bond breakage is rate-determining in TCE and cis-DCE transformation by ZVI. Two approaches were investigated to evaluate if isotope fractionation analysis can distinguish the effectiveness of transformation by ZVI as opposed to natural biodegradation. (i) Dual isotope plots. This study reports the first dual (C, Cl) element isotope plots for TCE and cis-DCE degradation by ZVI. The pattern for cis-DCE differs markedly from that reported for biodegradation of the same compound by KB-1, a commercially available Dehalococcoides-containing culture. The different trends suggest an expedient approach to distinguish abiotic and biotic transformation, but this needs to be confirmed in future studies. (ii) Product-related isotope fractionation. Carbon isotope ratios of the hydrogenolysis product cis

  7. Elemental and Isotopic Analysis of Uranium Oxide an NIST Glass Standards by FEMTOSECOND-LA-ICP-MIC-MS

    International Nuclear Information System (INIS)

    Ebert, Chris; Zamzow, Daniel S.; McBay, Eddie H.; Bostick, Debra A.; Bajic, Stanley J.; Baldwin, David P.; Houk, R.S.

    2009-01-01

    The objective of this work was to test and demonstrate the analytical figures of merit of a femtosecond-laser ablation (fs-LA) system coupled with an inductively coupled plasma-multi-ion collector-mass spectrometer (ICP-MIC-MS). The mobile fs-LA sampling system was designed and assembled at Ames Laboratory and shipped to Oak Ridge National Laboratory (ORNL), where it was integrated with an ICP-MIC-MS. The test period of the integrated systems was February 2-6, 2009. Spatially-resolved analysis of particulate samples is accomplished by 100-shot laser ablation using a fs-pulsewidth laser and monitoring selected isotopes in the resulting ICP-MS transient signal. The capability of performing high sensitivity, spatially resolved, isotopic analyses with high accuracy and precision and with virtually no sample preparation makes fs-LA-ICP-MIC-MS valuable for the measurement of actinide isotopes at low concentrations in very small samples for nonproliferation purposes. Femtosecond-LA has been shown to generate particles from the sample that are more representative of the bulk composition, thereby minimizing weaknesses encountered in previous work using nanosecond-LA (ns-LA). The improvement of fs- over ns-LA sampling arises from the different mechanisms for transfer of energy into the sample in these two laser pulse-length regimes. The shorter duration fs-LA pulses induce less heating and cause less damage to the sample than the longer ns pulses. This results in better stoichiometric sampling (i.e., a closer correlation between the composition of the ablated particles and that of the original solid sample), which improves accuracy for both intra- and inter-elemental analysis. The primary samples analyzed in this work are (a) solid uranium oxide powdered samples having different 235 U to 238 U concentration ratios, and (b) glass reference materials (NIST 610, 612, 614, and 616). Solid uranium oxide samples containing 235 U in depleted, natural, and enriched abundances were

  8. Stable water isotopic composition of the Antarctic subglacial Lake Vostok: implications for understanding the lake's hydrology.

    Science.gov (United States)

    Ekaykin, Alexey A; Lipenkov, Vladimir Y; Kozachek, Anna V; Vladimirova, Diana O

    2016-01-01

    We estimated the stable isotopic composition of water from the subglacial Lake Vostok using two different sets of samples: (1) water frozen on the drill bit immediately after the first lake unsealing and (2) water frozen in the borehole after the unsealing and re-drilled one year later. The most reliable values of the water isotopic composition are: -59.0 ± 0.3 ‰ for oxygen-18, -455 ± 1 ‰ for deuterium and 17 ± 1 ‰ for d-excess. This result is also confirmed by the modelling of isotopic transformations in the water which froze in the borehole, and by a laboratory experiment simulating this process. A comparison of the newly obtained water isotopic composition with that of the lake ice (-56.2 ‰ for oxygen-18, -442.4 ‰ for deuterium and 7.2 ‰ for d-excess) leads to the conclusion that the lake ice is very likely formed in isotopic equilibrium with water. In turn, this means that ice is formed by a slow freezing without formation of frazil ice crystals and/or water pockets. This conclusion agrees well with the observed physical and chemical properties of the lake's accreted ice. However, our estimate of the water's isotopic composition is only valid for the upper water layer and may not be representative for the deeper layers of the lake, so further investigations are required.

  9. An IBM-1620 code for calculaton of isotopic composition of irradiated uranium (ISOCOM-1)

    International Nuclear Information System (INIS)

    Soliman, R.H.; Karchava, G.; Hamouda, I.

    1974-01-01

    The present work gives a description of an IBM-1620 code to calculate the isotopic composition during the irradiation of a nuclear fuel, which initially consists of 235 U and 238 U. The numerical results of test calculations as well as the ET-RR-1 reactor calculations are presented. The code is in operation since 1968

  10. An IBM-1620 code for calculation of isotopic composition of irradiated thorium (ISOCOM-2)

    International Nuclear Information System (INIS)

    Soliman, R.H.; Karchava, G.; Hamouda, I.

    1978-01-01

    The present work gives a description of an IBM-1620 code to calculate the isotopic composition during the irradiation of a nuclear fuel, which initially contains 232 Th. The numerical results on test calculations are presented. The code has been in operation since 1968

  11. Review of data of oxygen and hydrogen isotope composition in thermal waters in China

    International Nuclear Information System (INIS)

    Fan Zhicheng; Wang Jiyang

    1988-01-01

    Based on the data of δD and δ 18 O content from more than 600 water samples, this paper reviews the stable isotope composition of thermal waters in China. Data to be used in this paper were mostly collected from published literatures with a few by authors. 9 figs, 2 tabs

  12. Habitat use and trophic position effects on contaminant bioaccumulation in fish indicated by stable isotope composition

    Science.gov (United States)

    The objective of our study was to determine the relationship between fish tissue stable isotope composition and total mercury or polychlorinated biphenyl (PCB) concentrations in a Great Lakes coastal food web. We sampled two resident fishes, Yellow Perch (Perca flavescens) and Bl...

  13. The atomic weight and isotopic composition of boron and their variation in nature

    International Nuclear Information System (INIS)

    Holden, N.E.

    1993-01-01

    The boron isotopic composition and atomic weight value and their variation in nature are reviewed. Questions are raised about the previously recommended value and the uncertainty for the atomic weight. The problem of what constitutes an acceptable range for normal material and what should then be considered geologically exceptional is discussed. Recent measurements make some previous decisions in need of re-evaluation

  14. Soil moisture effects on the carbon isotopic composition of soil respiration

    Science.gov (United States)

    The carbon isotopic composition ( 13C) of recently assimilated plant carbon is known to depend on water-stress, caused either by low soil moisture or by low atmospheric humidity. Air humidity has also been shown to correlate with the 13C of soil respiration, which suggests indir...

  15. Interpretation of groundwater origin in the Velenje coal mine on the basis of isotope composition

    Directory of Open Access Journals (Sweden)

    Janko Urbanc

    2002-12-01

    Full Text Available The aim of the investigation was to determine the isotopic properties of cave waters from the Velenje coal mine and define the recharge areas of individual aquifers. With regard to the oxygen isotope composition, groundwater in the Velenje coal mine can beclassified into three types. Typical d18O values of the first type are around -9 ‰ and are found in surface waters in the vicinity of the mine, therefore it is supposed that these waters are recharged locally. The second type is represented mainly by waters from thelower part of the pliocene aquifer. The average oxygen composition of these waters is about -11 ‰. This isotope composition is considerably different from the isotope composition of recent waters from the mine’s vicinity, which leads to the conclusion that these are older, fossile waters. These waters also have a very high degree of mineralization and consequently conductivity. Waters of the third type have average δ18O values around -10 ‰ and originate mainly from triassic dolomites. These waters could be a mixture of recentand old waters, but it is also possible that they flow into the coal mine from the higher areas of Paški Kozjak.

  16. Soil moisture effects on the carbon isotope composition of soil respiration

    Science.gov (United States)

    Claire L. Phillips; Nick Nickerson; David Risk; Zachary E. Kayler; Chris Andersen; Alan Mix; Barbara J. Bond

    2010-01-01

    The carbon isotopic composition (δ13C) of recently assimilated plant carbon is known to depend on water-stress, caused either by low soil moisture or by low atmospheric humidity. Air humidity has also been shown to correlate with the δ13C of soil respiration, which suggests indirectly that recently fixed photosynthates...

  17. The isotopic composition of soil organic carbon on a north - south transect in western Canada

    Czech Academy of Sciences Publication Activity Database

    Bird, M.; Šantrůčková, Hana; Lloyd, J.; Lawson, E.

    2002-01-01

    Roč. 53, - (2002), s. 393-403 ISSN 1351-0754 Institutional research plan: CEZ:AV0Z6066911 Keywords : isotopic composition * soil organic carbon * western Canada Subject RIV: EH - Ecology, Behaviour Impact factor: 1.452, year: 2002

  18. Isotope variations of dissolved Zn in the Rio Grande watershed, USA: The role of adsorption on Zn isotope composition

    Science.gov (United States)

    Szynkiewicz, Anna; Borrok, David M.

    2016-01-01

    In order to better understand the factors influencing zinc (Zn) isotope composition in hydrological systems, we analyzed the δ66Zn of dissolved Zn in the streams and groundwater of the Upper and Middle Rio Grande watershed in Colorado and New Mexico, United States. The stream water samples have a wider variation of δ66Zn (-0.57 to + 0.41 ‰ relative to the JMC 3-0749-Lyon standard) than groundwater samples (-0.13 to + 0.12 ‰) and than samples from streams that are in close proximity to abandoned mining sites (+0.24 to + 0.40 ‰). Regional changes of bedrock geology, from primarily igneous rocks to primarily sedimentary rocks, have no resolvable effect on the δ66Zn of aqueous samples. Instead, an increase in water pH from 7.5 to 8.5 corresponds to a considerable decrease in the δ66Zn of dissolved Zn (R2 = - 0.37, p = 0.003, n = 22). Consequently, we link the observed Zn isotope variations to the process of adsorption of Zn onto suspended sediment and bedrock minerals (average Δ66Znadsorbed-dissolved = + 0.31 ‰). Our results are in good agreement with previous experimental and empirical studies suggesting that Zn adsorption leads to a residual dissolved pool enriched in light Zn isotopes. Given that anthropogenic Zn sources can also be responsible for lowering of δ66Zn, and may overlap with the pH/adsorption effect on δ66Zn, the latter needs to be carefully considered in future studies to differentiate between natural and anthropogenic factors influencing Zn isotopes in this and other aquatic systems.

  19. A miniaturized laser-ablation mass spectrometer for in-situ measurements of isotope composition on solar body surfaces

    Science.gov (United States)

    Riedo, A.; Meyer, S.; Tulej, M.; Neuland, M.; Bieler, A.; Iakovleva, M.; Wurz, P.

    2012-04-01

    space instrument would have a cylindrical shape with a length of 120 mm, and a diameter of 60 mm, and a weight of about 1.5 kg (all electronics included). The mass analyzer supports high dynamic range of about 107 and a typical mass resolution of m/Δm~700. A computer-controlled optimizer controls the reproducibility of the performance of the mass analyzer, the laser fluence and the positioning of the sample. The system supports highly sensitive studies of elemental composition with sub-ppm detection limits. Our studies show that high accuracy and precision measurements can also be achieved in the investigations of isotopic patterns. Our initial studies of lead isotopic pattern indicated an accuracy and precision in the per mile range, which are comparable to that achieved by other - well known in isotopic analysis - mass spectrometric techniques, i.e., TIMS, SIMS, LA-ICP-MS used in the laboratory. The initial studies were conducted with Galena minerals and NIST standards. Hence, the miniaturized laser ablation time-of-flight mass spectrometer is a powerful instrument for in-situ measurements for the further investigation in surface characterization.

  20. Isotopic and trace element geochemistry of the Seligdar magnesiocarbonatites (South Yakutia, Russia): Insights regarding the mantle evolution beneath the Aldan-Stanovoy shield

    Science.gov (United States)

    Doroshkevich, Anna G.; Prokopyev, Ilya R.; Izokh, Andrey E.; Klemd, Reiner; Ponomarchuk, Anton V.; Nikolaeva, Irina V.; Vladykin, Nikolay V.

    2018-04-01

    The Paleoproterozoic Seligdar magnesiocarbonatite intrusion of the Aldan-Stanovoy shield in Russia underwent extensive postmagmatic hydrothermal alteration and metamorphic events. This study comprises new isotopic (Sr, Nd, C and O) data, whole-rock major and trace element compositions and trace element characteristics of the major minerals to gain a better understanding of the source and the formation process of the carbonatites. The Seligdar carbonatites have high concentrations of P2O5 (up to 18 wt%) and low concentrations of Na, K, Sr and Ba. The chondrite-normalized REE patterns of these carbonatites display significant enrichments of LREE relative to HREE with an average La/Ybcn ratio of 95. Hydrothermal and metamorphic overprints changed the trace element characteristics of the carbonatites and their minerals. These alteration processes were responsible for Sr loss and the shifting of the Sr isotopic compositions towards more radiogenic values. The altered carbonatites are further characterized by distinct 18O- and 13C-enrichments compared to the primary igneous carbonatites. The alteration most likely resulted from both the percolation of crustal-derived hydrothermal fluids and subsequent metamorphic processes accompanied by interaction with limestone-derived CO2. The narrow range of negative εNd(T) values indicates that the Seligdar carbonatites are dominated by a homogenous enriched mantle source component that was separated from the depleted mantle during the Archean.

  1. Long Fibre Composite Modelling Using Cohesive User's Element

    International Nuclear Information System (INIS)

    Kozak, Vladislav; Chlup, Zdenek

    2010-01-01

    The development glass matrix composites reinforced by unidirectional long ceramic fibre has resulted in a family of very perspective structural materials. The only disadvantage of such materials is relatively high brittleness at room temperature. The main micromechanisms acting as toughening mechanism are the pull out, crack bridging, matrix cracking. There are other mechanisms as crack deflection etc. but the primer mechanism is mentioned pull out which is governed by interface between fibre and matrix. The contribution shows a way how to predict and/or optimise mechanical behaviour of composite by application of cohesive zone method and write user's cohesive element into the FEM numerical package Abaqus. The presented results from numerical calculations are compared with experimental data. Crack extension is simulated by means of element extinction algorithms. The principal effort is concentrated on the application of the cohesive zone model with the special traction separation (bridging) law and on the cohesive zone modelling. Determination of micro-mechanical parameters is based on the combination of static tests, microscopic observations and numerical calibration procedures.

  2. Strontium-isotope composition in the Tethys Sea, Euboea, Greece

    International Nuclear Information System (INIS)

    Tremba, E.L.; Faure, G.; Summerson, C.H.

    1975-01-01

    The 37 Sr/ 36 Sr ratios of the Tethys Sea have been determined by analyzing limestones of Permian to Late Cretaceous age from the overthrusted sequence of central and northern Euboea. The results are in satisfactory agreement with ratios obtained by other investigators on unreplaced fossil shells of similar age collected elsewhere. The 37 Sr/ 36 Sr ratios of Mesozoic marbles from the autochtone metamorphic rocks of southern Euboea are more variable, perhaps because of increases in this ratio during regional metamorphism. Nevertheless, the lowest values of suites of isochronous samples may approach the correct ratio. Four samples of the Argyron Marble taken at different localities in southern Euboea and on the Attic peninsula have a concordant 87 Sr/ 86 Sr ratio of 0.70688+-0.00006 relative to 0.7080 for the Eimer and Amend isotope standard. This value indicates a Jurassic age for this formation even though the fragmentary fossil evidence favors a Late Cretaceous (Turonian) age

  3. Hydrochemistry and isotopic composition (δ"1"3C, δ"1"5N) in six dunes lagoons in the National Park of Lencois Maranhenses, Maranhao, Brazil

    International Nuclear Information System (INIS)

    Ramos Junior, Jayme Teixeira; Suzuki, Marina Satika; Meirelles, Brunele de Araujo; Rangel, Thiago Pessanha; Oliveira, Braulio Cherene Vaz de

    2015-01-01

    This study aims to evaluate the physicochemical parameters, nutrients and isotopic composition (δ"1"3C, δ"1"5N) of dissolved organic matter and MPS in six lakes located in the Maranhenses National Park, Maranhao State, under varying degrees of anthropic impact and distance from the sea. The physical and chemical parameters were measured in the field with portable devices; for total alkalinity, nutrients and photosynthetic pigments, samples were collected and analysed in the laboratory; the isotopic composition of carbon and nitrogen was determined from the particulate material retained on the filter and in the extract generated in the PPL filtration resin column. The limnological variables were assessed in both the dry and rainy seasons. The high rainfall caused a dilution effect for most of the elements studied in the rainy season. The elemental composition of the particulate fraction was 58% lower than the fraction dissolved. The carbon isotopic composition was lighter in the rainy season as a result of dilution and loading of allochthonous impoverished organic matter. (author)

  4. Anatomy of a cluster IDP. Part 2: Noble gas abundances, trace element geochemistry, isotopic abundances, and trace organic chemistry of several fragments from L2008#5

    Science.gov (United States)

    Thomas, K. L.; Clemett, S. J.; Flynn, G. J.; Keller, L. P.; Mckay, David S.; Messenger, S.; Nier, A. O.; Schlutter, D. J.; Sutton, S. R.; Walker, R. M.

    1994-01-01

    The topics discussed include the following: noble gas content and release temperatures; trace element abundances; heating summary of cluster fragments; isotopic measurements; and trace organic chemistry.

  5. REE and Isotopic Compositions of Lunar Basalts Demonstrate Partial Melting of Hybridized Mantle Sources after Cumulate Overturn is Required

    Science.gov (United States)

    Dygert, N. J.; Liang, Y.

    2017-12-01

    Lunar basalts maintain an important record of the composition of the lunar interior. Much of our understanding of the Moon's early evolution comes from studying their petrogenesis. Recent experimental work has advanced our knowledge of major and trace element fractionation during lunar magma ocean (LMO) crystallization [e.g., 1-3], which produced heterogeneous basalt sources in the Moon's mantle. With the new experimental constraints, we can evaluate isotopic and trace element signatures in lunar basalts in unprecedented detail, refining inferences about the Moon's dynamic history. Two petrogenetic models are invoked to explain the compositions of the basalts. The assimilation model argues they formed as primitive melts of early LMO cumulates that assimilated late LMO cumulates as they migrated upward. The cumulate overturn model argues that dense LMO cumulates sank into the lunar interior, producing hybridized sources that melted to form the basalts. Here we compare predicted Ce/Yb and Hf and Nd isotopes of partial melts of LMO cumulates with measured compositions of lunar basalts to evaluate whether they could have formed by end-member petrogenetic models. LMO crystallization models suggest all LMO cumulates have chondrite normalized Ce/Yb 1.5; these could not have formed by assimilation of any LMO cumulate or residual liquid (or KREEP basalt, which has isotopically negative ɛNd and ɛHf). In contrast, basalt REE patterns and isotopes can easily be modeled assuming partial melting of hybridized mantle sources, indicating overturn may be required. A chemical requirement for overturn independently confirms that late LMO cumulates are sufficiently low in viscosity to sink into the lunar interior, as suggested by recent rock deformation experiments [4]. Overturned, low viscosity late LMO cumulates would be relatively stable around the core [5]. High Ce/Yb basalts require that overturned cumulates were mixed back into the overlying mantle by convection within a few

  6. Modelling and Mapping Oxygen-18 Isotope Composition of Precipitation in Spain for Hydrologic and Climatic Applications

    International Nuclear Information System (INIS)

    Rodriguez-Arevalo, J.; Diaz-Teijeiro, M.F.; Castano, S.

    2011-01-01

    A simple multiple regression model based on two geographic factors (latitude and elevation) has been developed that reproduces reasonably well the spatial distribution of the current mean oxygen-18 isotope composition in precipitation over Spain. In a preliminary analysis, additional geographic and climatic factors do not improve the performance of the model. A continuous digital map of oxygen-18 isotope composition in precipitation has been produced by combining the polynomial model with a Digital Elevation Model using GIS tools. Application of the resulting map to several case studies in Spain has shown it to be useful as a reference of the isotope input function to groundwater recharge and surface runoff. The results obtained so far show a good fit between modelled stable isotope values and those measured in surface and ground waters from different aquifers and recharge areas. The GIS tools applied to a continuous digital layer of spatial isotope are able to provide accurate information at detailed scales that are not affordable by other means. Further validation of the model, and further testing of its usefulness in surface hydrology and climatic studies, is going on.

  7. Strontium and neodymium isotopic compositions in sediments from Godavari, Krishna and Pennar rivers

    International Nuclear Information System (INIS)

    Masood Ahmad, S.; Padmakumari, V.M.; Anil Babu, G.

    2009-01-01

    We report here strontium (Sr) and neodymium (Nd) isotopic compositions in bed sediments from the Godavari, Krishna and Pennar rivers, draining into the Bay of Bengal. The isotopic compositions of these sediments range from 0.7190 to 0.7610 for 87 Sr/ 86 Sr and -12.04 to -23.68 for ε Nd . This wide range in Sr and Nd isotopes is derived from variable proportions of sediments from different rock types in their drainage basins. All the three rivers have their characteristic isotopic signatures. The results display highest 87 Sr/ 86 Sr (0.7610) and most negative ε Nd values (-23.68) for the sediments of Pennar river. This is attributed to the chemical weathering of gneisses and granites in its drainage basin. The 87 Sr/ 86 Sr and ε Nd values for the Godavari river sediments range from 0.7196 to 0.7210 and -15.31 to -18.22 respectively. 87 Sr/ 86 Sr and ε Nd values in Krishna river sediments lie from 0.7217 to 0.7301 and -12.04 to -12.78 respectively. Our results show that the sedimentary load from the Godavari and Krishna rivers is primarily derived from the older rocks in their drainage basins. It is possible that the sediments transported through peninsular Indian rivers predominantly control Sr and Nd isotope sedimentary budget in the western Bay of Bengal. (author)

  8. An attempt to characterize certain organic and mineral substances by their stable isotope composition

    International Nuclear Information System (INIS)

    Bricout, J.; Fontes, J.C.; Letolle, R.; Mariotti, A.; Merlivat, L.

    1975-01-01

    The determination of the relative abundance of various stable isotopes - deuterium, oxygen-18, carbon-13, nitrogen-15, sulphur-34 - can be used to characterize the origin of a water body and of an organic or mineral substance in the environment. This results from the discovery that isotopic fractioning by living organisms occurs. The stable isotope composition of any substance reflects, at least partly, the various stages of its formation. A number of examples supporting this hypothesis are given. The passage of water through plants, or alcoholic fermentation, substantially modifies the stable isotope composition of water. The assimilation of atmospheric carbon dioxide involves a reduction in the carbon-13 content which varies depending on the enzymatic mechanism of photosynthesis. The enzymatic reactions that cause the biosynthesis of various organic substances in higher plants are accompanied by partial exclusion of deuterium, an exclusion which is greater or smaller depending on the biosynthesis pathway followed. The bacterial reduction of sulphur compounds involves a high rate of isotopic fractioning. As a result, industrial sulphates obtained by oxidation of reduced sulphur associated with hydrocarbon deposits are depleted in 34 S in comparison with natural sulphates. Similarly, the authors have observed that nitrates produced by the plant biological cycle are rich in nitrogen-15 compared to synthesized nitrates

  9. Variable Isotopic Compositions of Host Plant Populations Preclude Assessment of Aphid Overwintering Sites

    Directory of Open Access Journals (Sweden)

    Michael S. Crossley

    2017-12-01

    Full Text Available Soybean aphid (Aphis glycines Matsumura is a pest of soybean in the northern Midwest whose migratory patterns have been difficult to quantify. Improved knowledge of soybean aphid overwintering sites could facilitate the development of control efforts with exponential impacts on aphid densities on a regional scale. In this preliminary study, we explored the utility of variation in stable isotopes of carbon and nitrogen to distinguish soybean aphid overwintering origins. We compared variation in bulk 13C and 15N content in buckthorn (Rhamnus cathartica L. and soybean aphids in Wisconsin, among known overwintering locations in the northern Midwest. Specifically, we looked for associations between buckthorn and environmental variables that could aid in identifying overwintering habitats. We detected significant evidence of correlation between the bulk 13C and 15N signals of soybean aphids and buckthorn, despite high variability in stable isotope composition within and among buckthorn plants. Further, the 15N signal in buckthorn varied predictably with soil composition. However, lack of sufficient differentiation of geographic areas along axes of isotopic and environmental variation appears to preclude the use of carbon and nitrogen isotopic signals as effective predictors of likely aphid overwintering sites. These preliminary data suggest the need for future work that can further account for variability in 13C and 15N within/among buckthorn plants, and that explores the utility of other stable isotopes in assessing likely aphid overwintering sites.

  10. Methane Carbon Isotopic Composition Reveals Changing Production Pathways Across a Gradient of Permafrost Thaw

    Science.gov (United States)

    Rocci, K.; Burke, S. A.; Clariza, P.; Malhotra, A.; McCalley, C. K.; Verbeke, B. A.; Werner, S. L.; Roulet, N. T.; Varner, R. K.

    2017-12-01

    Methane (CH4) emission in areas of discontinuous permafrost may increase with warming temperatures resulting in a positive feedback to climate change. Characterizing the production pathways of CH4, which may be inferred by measuring carbon isotopes, can help determine underlying mechanistic changes. We studied CH4 flux and isotopic composition of porewater (δ13C-CH4) in a sub-arctic peatland in Abisko, Sweden to understand controls on these factors across a thaw gradient during four growing seasons. Methane chamber flux measurements and porewater samples were collected in July 2013, and over the growing seasons of 2014 to 2016. Samples were analyzed on a Gas Chromatograph with a Flame Ionization Detector for CH4 concentrations and a Quantum Cascade Laser for carbon isotopes. Increased emission rates and changing isotopic signatures were observed across the thaw gradient throughout the growing season. While CH4 flux increased with increases in temperature and shallower water table, δ13C-CH4 exhibited a seasonal pattern that did not correlate with measured environmental variables, suggesting dependence on other factors. The most significant controlling factor for both flux and isotopic signature was plant community composition, specifically, the presence of graminoid species. Graminoid cover increases with thaw stage so both CH4 emissions and δ13C-CH4 are likely to increase in a warmer world, suggesting a shift toward the acetoclastic pathway of methane production.

  11. Evaluation of elemental composition of clays from Campos Gerais (MG)

    International Nuclear Information System (INIS)

    Martins, Joao P.M.; Maduar, Marcelo F.; Silva, Paulo S.C da

    2013-01-01

    There are numerous applications given to clays including oil and water adsorbent, ceramic, whitening of beverages, porcelain, waste treatment, organic carrier molecules in cosmetics and pharmaceuticals, support for catalysts. In the pharmaceutical industry, the clays are used as excipients, diluents, desiccants, emulsifiers, to mask undesirable flavors, isotonic agent such as charger and delivery of active substances. These characteristics have contributed to the expansion of the search for applications of clay minerals in the cosmetic industry. The aim of this study was to determine the elemental composition of clays from Campos Gerais, Minas Gerais, with a view to their applicability in the production of cosmetics. The elements As, Ba, Br, Ce, Cl, Co, Cr, Cs, Eu, Fe, Hf, K, La, Lu, Na, Nd, Rb, Sb, Sc, Sm, Ta, Tb, Th,U, Yb and Zn were determined by neutron activation analysis and radionuclide activity concentration of 226 Ra, 228 Ra, 210 Pb and 40 K were determined by gamma spectrometry. It was verified that the activity concentration of radionuclides was in the same concentration as the global average, indicating that these samples do not present a risk of increased radiation exposure. The concentration of most elements determined is less than or equal to the overall mean concentrations, indicated by the values of Continental Upper Crust. (author)

  12. Toxic element composition of multani mitti clay for nutritional safety

    International Nuclear Information System (INIS)

    Waheed, S.; Faiz, Y.; Rahman, S.; Siddique, N.

    2013-01-01

    Geophagy of multani mitti (MM) clay is very common in central Pakistan especially amongst women. It was therefore mandatory to establish baseline levels of toxic elements in this clay for its safe dietary consumption by consumers of different genders, age groups and physical states. Instrumental neutron activation analysis and atomic absorption spectrometry techniques were used to determine the nutritional safety of MM clay for oral intake. All quantified toxic elements were detected at trace levels with composition in the descending order; Pb > Br > As > Sb > Hg > Cd. Comparison of these elements in MM clay with other clays shows that As, Cd, and Pb, are lowest in MM clay while its Br and Hg contents are high. Highest weekly dietary intakes of As, Br, Cd, Hg, and Sb were found to be 18, 0.05, 1.6, 9.2 and 1.1 % of the respective recommended provisional tolerable weekly intakes. The findings of this study show that As, Br, Cd, Hg and Sb in MM clay are well below the tolerance levels. However its Pb concentration is very high and may pose health concerns. The data presented in this study can be used as national base level guideline for geophagy of MM clay by men, women (normal, pregnant and lactating) and children. (author)

  13. Elemental composition of betel nut and associated chewing materials

    International Nuclear Information System (INIS)

    Ridge, C.; Akanle, O.; Spyrou, N.M.

    2001-01-01

    Betel nut chewing (Area catechu), Whether plain or wrapped inside a betel leaf 'quid' together with other substances including tobacco, has been reported as a cause of the high incidence of oral and oesophageal cancers in Asian communities worldwide. Chewing of such substances results in the formation of nitrosamines, some of which may be diabetogenic to man. The incidence of Type 2 diabetes is particularly prevalent amongst Asian immigrants living in the UK and as part of a larger study we have analysed a number of popular betel nut based chewing materials to determine their elemental composition. Instrumental neutron activation analysis was used for determination of elemental concentrations of short-lived radionuclides. Ag, Al. Br, Ca, Cl, Cu, Dy, K, Mg, Mn, Na, Ti, and V were detected, some of which are implicated in diabetes. Concentrations of these, expect for Ag, Dy and Ti, are reported and compared with values found in betel-nut and chewing materials from Taiwan. It is indicated that for certain elements the amount ingested by betel-nut chewers may be a significant fraction of their daily dietary intake. (author)

  14. Trace element composition in sediments of the Amazonian Lake Cristalino

    International Nuclear Information System (INIS)

    Ferraz, E.S.B.; Fernandes, E.A.N.

    1995-01-01

    Lake Cristalino is a small lake adjacent to the Negro River near Manaus and not far from the Amazonas River, in the central Amazon basin. The lake is fed seasonally by waters of the Negro River, a blackwater river with low levels of nutrients and suspended solids (7 g m -3 ). However, some investigations have established that Lake Cristalino has a high sedimentation rate (0.4-0.5 cm year -l ) similar to those in the alluvial floodplain lakes of the Amazonas River (suspended solids 200-300 g m -3 ). Sediment cores were taken during the low-water period and the trace-element composition and the natural radioactivity in the lake were examined. The results show a core (31 cm length) relatively uniform in concentrations of trace elements (Br, Ce, Co, Cr, Cs, Eu, Fe, Hf, La, Sc, Sm, Ta, Tb, Th, Yb and Zn), and the presence of 137 Cs in the first half. Concentrations of trace elements in Lake Cristalino sediments were not correlated with concentrations in the sediments of its parent river, the Negro River, or with concentrations in soils of the local area. However, significant correlation was found between the sediments of the lake and those of the Amazonas River. On the basis of these results, and water-level data at Manaus port, it is concluded that the lake occasionally receives variable amounts of sediment from the Amazonas River. 10 refs., 2 tabs., 2 figs

  15. Karst springs as 'natural' pluviometers: Constraints on the isotopic composition of rainfall in the Apennines of central Italy

    International Nuclear Information System (INIS)

    Minissale, A.; Vaselli, O.

    2011-01-01

    Highlights: → Isotopic compositions of karstic springs in central Italy have been reviewed. → Isotopic gradients of rainfalls for elevations have been evaluated in an Alpine valley. → Karstic drops have been calculated by using isotopic compositions of springs. → Isotopic compositions of rainfalls in central Italy have been re-calculated using the isotopic compositions of karstic springs. - Abstract: This paper describes an indirect method to calculate the isotopic composition of rainfall by using the isotopic composition of karst springs fed by waters circulating in the most important regional aquifer of central Italy, i.e. the Mesozoic limestone sequence that forms the backbone of the Apennines. By using δ 18 O and δD data and the δ 18 O (and/or δD) average gradient for elevation, evaluated through the use of literature rainfall data and new measurements from a typical Alpine valley in northern Italy, the altitude of precipitation of their parent water has been re-calculated. Vertical descents of more than 2000 m, from recharge to discharge, have been assessed in some high flow-rate cold springs in the morphologically steep Adriatic sector of central Italy. A clear correlation between the vertical descents and more negative isotopic compositions at their relative emergence elevations is highlighted. In contrast, in the Tyrrhenian sector lower karstic drops (generally lower than 500 m) correlate with less negative isotopic composition of recharge areas. The δ 18 O iso-contour map of the 'recalculated' parent rainfall in central Italy is more detailed than any possible isotopic map of rainfall made using pluviometers, unless large number of rainfall collectors were deployed on mountaintops. The data also show that the isotopic composition of rainfall depends on the source of the storm water. In particular, precipitation is isotopically heavier when originating in the Mediterranean Sea, and lighter when formed in the Atlantic Ocean. Consequently, the

  16. Finite element analysis of composite concrete-timber beams

    Directory of Open Access Journals (Sweden)

    N. C. S. FORTI

    Full Text Available AbstractIn the search for sustainable construction, timber construction is gaining in popularity around the world. Sustainably harvested wood stores carbon dioxide, while reforestation absorbs yet more CO2. One technique involves the combination of a concrete slab and a timber beam, where the two materials are assembled by the use of flexible connectors. Composite structures provide reduced costs, environmental benefits, a better acoustic performance, when compared to timber structures, and maintain structural safety. Composite structures combine materials with different mechanical properties. Their mechanical performance depends on the efficiency of the connection, which is designed to transmit shear longitudinal forces between the two materials and to prevent vertical detachment. This study contributes with the implementation of a finite element formulation for stress and displacement determination of composite concrete-timber beams. The deduced stiffness matrix and load vector are presented along to numerical examples. Numerical examples are compared to the analytical equations available in Eurocode 5 and to experimental data found in the literature.

  17. Monitoring of chemical and isotopic composition of the Euphrates river in Syria

    International Nuclear Information System (INIS)

    Kattan, Z.

    2008-11-01

    The ratios of stable isotopes ( 18 O and 2 H), tritium content, together with the chemical composition of major ions of the Euphrates and Balikh (Euphrates tributary) Rivers, and the groundwaters of four wells drilled close to the Euphrates River course, were measured on a monthly basis. The Euphrates River water was monitored at twelve stations along its course in Syria during the period from January 2004 to December 2006, whereas those of the Balikh and groundwaters were only investigated during 2005. Although, the spatial variations of heavy stable isotope concentrations are moderated with respect to other large rivers in the world, the concentrations of these isotopes increase generally downstream the Euphrates River, with a sharp enrichment at Al-Assad Lake. This sharp increase could be explained by the effect of direct evaporation from the river and its tributaries; and the effect of drainage return flows of irrigation waters, isotopically more enriched. Enrichment of stable isotopes in the Euphrates River water was used as a direct indicator of evaporation. Based on an experimental evaporation result of a Euphrates water sample and the integral enrichment of heavy stable isotopes in the Euphrates River system, the amount of water losses by evaporation from Al-Assad Lake was estimated to be about 1.26 to 1.62 billion m''3, according to 18 O and deuterium ( 2 H), respectively. This amount represents about 12-16% of the renewable surface water resources in the country. (author)

  18. Stable bromine isotopic composition of methyl bromide released from plant matter

    Science.gov (United States)

    Horst, Axel; Holmstrand, Henry; Andersson, Per; Thornton, Brett F.; Wishkerman, Asher; Keppler, Frank; Gustafsson, Örjan

    2014-01-01

    Methyl bromide (CH3Br) emitted from plants constitutes a natural source of bromine to the atmosphere, and is a component in the currently unbalanced global CH3Br budget. In the stratosphere, CH3Br contributes to ozone loss processes. Studies of stable isotope composition may reduce uncertainties in the atmospheric CH3Br budget, but require well-constrained isotope fingerprints of the source end members. Here we report the first measurements of stable bromine isotopes (δ81Br) in CH3Br from abiotic plant emissions. Incubations of both KBr-fortified pectin, a ubiquitous cell-stabilizing macromolecule, and of a natural halophyte (Salicornia fruticosa), yielded an enrichment factor (ε) of -2.00 ± 0.23‰ (1σ, n = 8) for pectin and -1.82 ± 0.02‰ (1σ, n = 4) for Salicornia (the relative amount of the heavier 81Br was decreased in CH3Br compared to the substrate salt). For short incubations, and up to 10% consumption of the salt substrate, this isotope effect was similar for temperatures from 30 up to 300 °C. For longer incubations of up to 90 h at 180 °C the δ81Br values increased from -2‰ to 0‰ for pectin and to -1‰ for Salicornia. These δ81Br source signatures of CH3Br formation from plant matter combine with similar data for carbon isotopes to facilitate multidimensional isotope diagnostics of the CH3Br budget.

  19. Natural Ca Isotope Composition of Urine as a Rapid Measure of Bone Mineral Balance

    Science.gov (United States)

    Skulan, J.; Gordon, G. W.; Morgan, J.; Romaniello, S. J.; Smith, S. M.; Anbar, A. D.

    2011-12-01

    Naturally occurring stable Ca isotope variations in urine are emerging as a powerful tool to detect changes in bone mineral balance. Bone formation depletes soft tissue of light Ca isotopes while bone resorption releases isotopically light Ca into soft tissue. Previously published work found that variations in Ca isotope composition could be detected at 4 weeks of bed rest in a 90-day bed rest study (data collected at 4, 8 and 12 weeks). A new 30-day bed rest study involved 12 patients on a controlled diet, monitored for 7 days prior to bed rest and 7 days post bed rest. Samples of urine, blood and food were collected throughout the study. Four times daily blood samples and per void urine samples were collected to monitor diurnal or high frequency variations. An improved chemical purification protocol, followed by measurement using multiple collector inductively coupled plasma mass spectrometry (MC-ICP-MS) allowed accurate and precise determinations of mass-dependent Ca isotope variations in these biological samples to better than ±0.2% (δ44/42Ca) on studies as seen by X-ray measurements. This Ca isotope technique should accelerate the pace of discovery of new treatments for bone disease and provide novel insights into the dynamics of bone metabolism.

  20. Coordinated Oxygen Isotopic and Petrologic Studies of CAIS Record Varying Composition of Protosolar

    Science.gov (United States)

    Simon, Justin I.; Matzel, J. E. P.; Simon, S. B.; Weber, P. K.; Grossman, L.; Ross, D. K.; Hutcheon, I. D.

    2012-01-01

    Ca-, Al-rich inclusions (CAIs) record the O-isotope composition of Solar nebular gas from which they grew [1]. High spatial resolution O-isotope measurements afforded by ion microprobe analysis across the rims and margin of CAIs reveal systematic variations in (Delta)O-17 and suggest formation from a diversity of nebular environments [2-4]. This heterogeneity has been explained by isotopic mixing between the O-16-rich Solar reservoir [6] and a second O-16-poor reservoir (probably nebular gas) with a "planetary-like" isotopic composition [e.g., 1, 6-7], but the mechanism and location(s) where these events occur within the protoplanetary disk remain uncertain. The orientation of large and systematic variations in (Delta)O-17 reported by [3] for a compact Type A CAI from the Efremovka reduced CV3 chondrite differs dramatically from reports by [4] of a similar CAI, A37 from the Allende oxidized CV3 chondrite. Both studies conclude that CAIs were exposed to distinct, nebular O-isotope reservoirs, implying the transfer of CAIs among different settings within the protoplanetary disk [4]. To test this hypothesis further and the extent of intra-CAI O-isotopic variation, a pristine compact Type A CAI, Ef-1 from Efremovka, and a Type B2 CAI, TS4 from Allende were studied. Our new results are equally intriguing because, collectively, O-isotopic zoning patterns in the CAIs indicate a progressive and cyclic record. The results imply that CAIs were commonly exposed to multiple environments of distinct gas during their formation. Numerical models help constrain conditions and duration of these events.

  1. The distribution of lead concentrations and isotope compositions in the eastern Tropical Atlantic Ocean

    Science.gov (United States)

    Bridgestock, Luke; Rehkämper, Mark; van de Flierdt, Tina; Paul, Maxence; Milne, Angela; Lohan, Maeve C.; Achterberg, Eric P.

    2018-03-01

    Anthropogenic emissions have dominated marine Pb sources during the past century. Here we present Pb concentrations and isotope compositions for ocean depth profiles collected in the eastern Tropical Atlantic Ocean (GEOTRACES section GA06), to trace the transfer of anthropogenic Pb into the ocean interior. Variations in Pb concentration and isotope composition were associated with changes in hydrography. Water masses ventilated in the southern hemisphere generally featured lower 206Pb/207Pb and 208Pb/207Pb ratios than those ventilated in the northern hemisphere, in accordance with Pb isotope data of historic anthropogenic Pb emissions. The distributions of Pb concentrations and isotope compositions in northern sourced waters were consistent with differences in their ventilation timescales. For example, a Pb concentration maximum at intermediate depth (600-900 m, 35 pmol kg-1) in waters sourced from the Irminger/Labrador Seas, is associated with Pb isotope compositions (206Pb/207Pb = 1.1818-1.1824, 208Pb/207Pb = 2.4472-2.4483) indicative of northern hemispheric emissions during the 1950s and 1960s close to peak leaded petrol usage, and a transit time of ∼50-60 years. In contrast, North Atlantic Deep Water (2000-4000 m water depth) featured lower Pb concentrations and isotope compositions (206Pb/207Pb = 1.1762-1.184, 208Pb/207Pb = 2.4482-2.4545) indicative of northern hemispheric emissions during the 1910s and 1930s and a transit time of ∼80-100 years. This supports the notion that transient anthropogenic Pb inputs are predominantly transferred into the ocean interior by water mass transport. However, the interpretation of Pb concentration and isotope composition distributions in terms of ventilation timescales and pathways is complicated by (1) the chemical reactivity of Pb in the ocean, and (2) mixing of waters ventilated during different time periods. The complex effects of water mass mixing on Pb distributions is particularly apparent in seawater in the

  2. Holocene elemental, lead isotope and charcoal record from peat in southern Poland

    Directory of Open Access Journals (Sweden)

    K. Tudyka

    2017-03-01

    Full Text Available This article presents a mid-resolution elemental, isotopic and charcoal record from 10700 BC to AD 500 in a peat core located in Żyglin (southern Poland. The objective is to give insight into the proxies with emphasis on lead (Pb sources in this minerogenic peat deposit. During the Early Holocene (10700–7550 BC the average 206Pb/207Pb quotient was around 1.196. This isotopic signature is consistent with natural dust derived from long-distance soil and rock weathering. The Mid-Holocene period (7550–3200 BC shows a significant change in the peat accumulation conditions. The growth rate is approximately 0.04 mm yr-1 and the 206Pb/207Pb quotients are shifted toward values that are found in local galena ores. This is simultaneous with a significantly increased lead flux which further confirms local sources of material in this peat deposit. In the Late Holocene period (3200 BC–AD 500 a large quantity of charcoal particles with diameters ranging from 2 mm up to 3 cm is found; also, Pb, Zn and Cu fluxes reach their highest values. This period corresponds to the Eneolithic, Bronze and Iron Ages, and human impact is recorded as charcoal.

  3. Chemical and Oxygen Isotopic Composition of Roman and Late Antique Glass from Northern Greece

    Directory of Open Access Journals (Sweden)

    Alberta Silvestri

    2017-01-01

    Full Text Available The present paper emphasizes the importance of measuring the oxygen isotopic and chemical compositions of ancient glass, in order to constrain some features such as age, raw materials, and production technologies and to identify the “fingerprint” of local productions. In this context, thirty-nine Roman and late Antique glass samples and eight chert samples from northern Greece were selected and analysed for their oxygen isotopic and chemical compositions. Results show that the majority of glass samples are produced using natron as flux and have δ18O values of about 15.5‰, plus or minus a few tenths of one per mil, suggesting that raw materials probably come from Levantine area. Four samples are heavily enriched in 18O, and their chemical composition clearly shows that they were made with soda plant ash as flux. Isotopic and chemical data of Greek chert samples support the hypothesis of local production of the above samples. About half of the glass samples have chemical compositions, which allow their age to be constrained to the late Antique period. For the remaining glass, similarities with literature compositional groups are reported and discussed.

  4. Changes in Chemical and Isotopic Composition of Groundwater During a Long Term Pumping Test in Brestovica Karst Aquifer

    Energy Technology Data Exchange (ETDEWEB)

    Mezga, K.; Urbanc, J. [Geological Survey of Slovenia, Department of Hydrogeology, Ljubljana (Slovenia)

    2013-07-15

    A pumping test of the Klarici water supply near Brestovica was performed in August 2008, in order to determine the karst groundwater resource capacity. Groundwater was pumped for a month with a total capacity of 470 L/s. During the experiment, sampling for chemical and isotopic composition of groundwater and surface water was carried out. Intensive pumping in dry meteorological conditions caused a lowering of the water table and changes in the chemical and isotopic composition of pumped water. Local meteoric waters are infiltrated into the aquifer at a lower mean altitude; therefore the {delta}{sup 18}O is enriched with the heavy oxygen isotope. The duration of pumping resulted in changes in the isotopic composition of oxygen due to a greater impact of the intergranular Soca River aquifer on the karst aquifer. On the basis of isotope composition it was possible to quantify the impact of the Soca River on the karst aquifer. (author)

  5. Data book of the isotopic composition of spent fuel in light water reactors

    International Nuclear Information System (INIS)

    Naito, Yoshitaka; Kurosawa, Masayoshi; Kaneko, Toshiyuki.

    1994-03-01

    In the framework of the activity of the working group on Evaluation of Nuclide Generation and Depletion in the Japanese Nuclear Data Committee, we summarized the assay data of the isotopic composition of LWR spent fuels in order to verify the accuracy of the burnup calculation codes. The report contains the data collected from the 13 light water reactors (LWRs) including the 9 LWRs (5 PWRs and 4 BWRs) in Europe and USA, the 4 LWRs (2 PWRs and 2 BWRs) in Japan. The collected data were sorted into the irradiation history of the fuel samples, the composition of the fuel assemblies, the sampling position and the isotopic composition of the fuel samples. (author)

  6. Isotopic composition of nitrate and particulate organic matter in a pristine dam reservoir of western India: Implications for biogeochemical processes

    Digital Repository Service at National Institute of Oceanography (India)

    Bardhan, P.; Naqvi, S.W.A.; Karapurkar, S.G.; Shenoy, D.M.; Kurian, S.; Naik, H.

    , 767–779, 2017 www.biogeosciences.net/14/767/2017/ doi:10.5194/bg-14-767-2017 © Author(s) 2017. CC Attribution 3.0 License. Isotopic composition of nitrate and particulate organic matter in a pristine dam reservoir of western India: implications... basis. Samples for nitrate isotopic measurements were col- lected from 2011. The facility for nitrate isotope analysis was Biogeosciences, 14, 767–779, 2017 www.biogeosciences.net/14/767/2017/ P. Bardhan et al.: Isotopic composition of nitrate and POM...

  7. Influence of size and surface structure of microparticles on accuracy of measurements of its uranium isotopic composition

    International Nuclear Information System (INIS)

    Stebelkov, V.; Kolesnikov, O.; Moulenko, D.; Sokolov, A.; Pavlov, A.; Simakin, S.

    2002-01-01

    Full text: One of the elements of the scheme for complex analysis of environmental samples, collected in the regions of location of nuclear facilities, is mass-spectrometry of microparticles of nuclear materials implemented for determination of isotopic composition of these materials. Widely used technique of mass-spectrometry of particles is secondary ion mass-spectrometry. This technique is characterized by successive acquisition of ions from different isotopes under gradual sputtering of microparticle during analysis. The purpose of this work was investigation of kinetic of size changing and changing of measured values of uranium-235 concentration as well as investigation of influence of size and surface structure of microparticle on measurement results. Method of investigation had been comprised to several sequential measurements of uranium isotopes content in the same particle and photography of this particle before every sequential measurement by using electron microscope. Analysis of each particle was finished when this particle was fully sputtered. There were investigated 33 particles of irregular shape and initial sizes from 0.5 μm to 3.5 μm. These particles had different types of surface structure and different isotopic composition. Besides there were investigated 22 spherical particles of UO 2 with 3.7% uranium-235 abundance with sizes from 0.7 μm to 2.4 μm. Thirteen particles of irregular shape were sputtered fully during first measurement of isotopic composition. Two sequential measurements were implemented for 12 particles, three sequential measurements were implemented for 7 particles. For 2 particles of sizes 3.5 μm x 2 μm and 1.2 μm there were implemented four sequential measurements of isotopic composition. During these investigations it was determined that the number of sequential measurements depends not only on size but also on surface structure of particle. With rare exception the sequential values of concentrations of uranium-235

  8. Neural network applied to elemental archaeological Marajoara ceramic compositions

    International Nuclear Information System (INIS)

    Toyota, Rosimeiri G.; Munita, Casimiro S.; Boscarioli, Clodis

    2009-01-01

    In the last decades several analytical techniques have been used in archaeological ceramics studies. However, instrumental neutron activation analysis, INAA, employing gamma-ray spectrometry seems to be the most suitable technique because it is a simple analytical method in its purely instrumental form. The purpose of this work was to determine the concentration of Ce, Co, Cr, Cs, Eu, Fe, Hf, K, La, Lu, Na, Nd, Rb, Sb, Sc, Sm, Ta, Tb, Th, U, Yb, and Zn in 160 original marajoara ceramic fragments by INAA. Marajoara ceramics culture was sophisticated and well developed. This culture reached its peak during the V and XIV centuries in Marajo Island located on the Amazon River delta area in Brazil. The purpose of the quantitative data was to identify compositionally homogeneous groups within the database. Having this in mind, the data set was first converted to base-10 logarithms to compensate for the differences in magnitude between major elements and trace elements, and also to yield a closer to normal distribution for several trace elements. After that, the data were analyzed using the Mahalanobis distance and using the lambda Wilks as critical value to identify the outliers. The similarities among the samples were studied by means of cluster analysis, principal components analysis and discriminant analysis. Additional confirmation of these groups was made by using elemental concentration bivariate plots. The results showed that there were two very well defined groups in the data set. In addition, the database was studied using artificial neural network with unsupervised learning strategy known as self-organizing maps to classify the marajoara ceramics. The experiments carried out showed that self-organizing maps artificial neural network is capable of discriminating ceramic fragments like multivariate statistical methods, and, again the results showed that the database was formed by two groups. (author)

  9. A non-terrestrial 16O-rich isotopic composition for the protosolar nebula.

    Science.gov (United States)

    Hashizume, Ko; Chaussidon, Marc

    2005-03-31

    The discovery in primitive components of meteorites of large oxygen isotopic variations that could not be attributed to mass-dependent fractionation effects has raised a fundamental question: what is the composition of the protosolar gas from which the host grains formed? This composition is probably preserved in the outer layers of the Sun, but the resolution of astronomical spectroscopic measurements is still too poor to be useful for comparison with planetary material. Here we report a precise determination of the oxygen isotopic composition of the solar wind from particles implanted in the outer hundreds of nanometres of metallic grains in the lunar regolith. These layers of the grains are enriched in 16O by >20 +/- 4 per thousand relative to the Earth, Mars and bulk meteorites, which implies the existence in the solar accretion disk of reactions--as yet unknown--that were able to change the 17O/16O and 18O/16O ratios in a way that was not dependent strictly on the mass of the isotope. Photochemical self-shielding of the CO gas irradiated by ultraviolet light may be one of these key processes, because it depends on the abundance of the isotopes, rather than their masses.

  10. Isotope composition and volume of Earth´s early oceans

    DEFF Research Database (Denmark)

    Pope, Emily Catherine; Bird, Dennis K.; Rosing, Minik Thorleif

    2012-01-01

    Oxygen and hydrogen isotope compositions of Earth´s seawater are controlled by volatile fluxes among mantle, lithospheric (oceanic and continental crust), and atmospheric reservoirs. Throughout geologic time the oxygen mass budget was likely conserved within these Earth system reservoirs, but hyd...... in Earth´s oceans. Our calculations predict that the oceans of early Earth were up to 26% more voluminous, and atmospheric CH4 and CO2 concentrations determined from limits on hydrogen escape to space are consistent with clement conditions on Archaean Earth.......Oxygen and hydrogen isotope compositions of Earth´s seawater are controlled by volatile fluxes among mantle, lithospheric (oceanic and continental crust), and atmospheric reservoirs. Throughout geologic time the oxygen mass budget was likely conserved within these Earth system reservoirs......, but hydrogen´s was not, as it can escape to space. Isotopic properties of serpentine from the approximately 3.8 Ga Isua Supracrustal Belt in West Greenland are used to characterize hydrogen and oxygen isotope compositions of ancient seawater. Archaean oceans were depleted in deuterium [expressed as Î...

  11. Boron Isotopic Composition of Metasomatized Mantle Xenoliths from the Western Rift, East Africa

    Science.gov (United States)

    Hudgins, T.; Nelson, W. R.

    2017-12-01

    The Western Branch of the East African Rift System is known to have a thick lithosphere and sparse, alkaline volcanism associated with a metasomatized mantle source. Recent work investigating the relationship between Western Branch metasomatized mantle xenoliths and associated lavas has suggested that these metasomes are a significant factor in the evolution of the rift. Hydrous/carbonated fluids or silicate melts are potent metasomatic agents, however gaining insight into the source of a metasomatic agent proves challenging. Here we investigate the potential metasomatic fluid sources using B isotope analysis of mineral separates from Western Branch xenoliths. Preliminary SIMS analyses of phlogopite from Katwe Kikorongo and Bufumbira have and average B isotopic composition of -28.2‰ ± 5.1 and -16.4‰ ± 3.6, respectively. These values are are dissimilar to MORB (-7.5‰ ± 0.7; Marschall and Monteleone, 2015), primitive mantle (-10‰ ± 2; Chaussidon and Marty, 1995), and bulk continental crust (-9.1‰ ± 2.4; Marschall et al., 2017) and display significant heterogeneity across a relatively short ( 150km) portion of the Western Branch. Though displaying large variability, these B isotopic compositions are indicative of a metasomatic agent with a more negative B isotopic composition than MORB, PM, or BCC. These results are consistent with fluids that released from a subducting slab and may be related to 700 Ma Pan-African subduction.

  12. 1987 target values for uncertainty components in fissile isotope and element assay

    International Nuclear Information System (INIS)

    De Bievre, P.; Baumann, S.; Gorgenyi, T.; Kuhn, E.; Deron, S.; Dalton, J.; Perrin, R.E.; Pietri, C.; De Regge, P.

    1987-01-01

    The Working Group on Techniques and Standards for Destructive Analysis (WGDA) of the European Safeguards Research and Development Association (ESARDA), which at present includes the representation of 37 nuclear analytical laboratories, has long been concerned with defining realistic performance characteristics of destructive analysis techniques. One of the terms of reference of the working groups is: ''to evaluate and recommend criteria for destructive analysis of nuclear materials for use by plant operators and safeguarding authorities''. Some of the most important and most badly needed criteria are those to be used for judging results of quantitative determinations of fissile isotope and element amounts. The working group has recognized and discussed this problem at several meetings and decided that it was appropriate to fix reasonable levels of performance as ''goals'' for nuclear analytical laboratories

  13. Element distribution and noble gas isotopic abundances in lunar meteorite Allan Hills A81005

    International Nuclear Information System (INIS)

    Kraehenbuehl, U.; Eugster, O.; Niedermann, S.

    1986-01-01

    Antarctic meteorite ALLAN HILLS A81005, an anorthositic breccia, is recognized to be of lunar origin. The noble gases in this meteorite were analyzed and found to be solar-wind implanted gases, whose absolute and relative concentrations are quite similar to those in lunar regolith samples. A sample of this meteorite was obtained for the analysis of the noble gas isotopes, including Kr(81), and for the determination of the elemental abundances. In order to better determine the volume derived from the surface correlated gases, grain size fractions were prepared. The results of the instrumental measurements of the gamma radiation are listed. From the amounts of cosmic ray produced noble gases and respective production rates, the lunar surface residence times were calculated. It was concluded that the lunar surface time is about half a billion years

  14. Elemental and isotopic imaging of biological samples using NanoSIMS.

    Science.gov (United States)

    Kilburn, Matt R; Clode, Peta L

    2014-01-01

    With its low detection limits and the ability to analyze most of the elements in the periodic table, secondary ion mass spectrometry (SIMS) represents one of the most versatile in situ analytical techniques available, and recent developments have resulted in significant advantages for the use of imaging mass spectrometry in biological and biomedical research. Increases in spatial resolution and sensitivity allow detailed interrogation of samples at relevant scales and chemical concentrations. Advances in dynamic SIMS, specifically with the advent of NanoSIMS, now allow the tracking of stable isotopes within biological systems at subcellular length scales, while static SIMS combines subcellular imaging with molecular identification. In this chapter, we present an introduction to the SIMS technique, with particular reference to NanoSIMS, and discuss its application in biological and biomedical research.

  15. Oxigen isotope compositions as indicators of epidote granite genesis in the Borborema Provinces, NE Brazil

    International Nuclear Information System (INIS)

    Ferreira, V.P.; Valley, J.W; Sial, A.N; Spicuzza, M.J

    2001-01-01

    Neoproterozoic magmatic epidote-bearing granitoids intrude low-grade metapelites in the Cachoeirinha-Salgueiro terrane (CST), and gneisses and migmatites in the Serido terrane (ST), in the Borborema structural province, northeastern Brazil. Granitoids in both terranes contain biotite and hornblende, and are metaluminous, calc-alkalic, and oxidized I-type granites according to White's (1992) classification. However, in spite of these similarities, this work shows that mineral oxygen isotope data from plutons of the two terranes indicate different magma sources, and that magmatic epidote besides crystallizing at different pressure conditions, can have variable isotopic composition (au)

  16. The Oxygen Isotopic Composition of MIL 090001: A CR2 Chondrite with Abundant Refractory Inclusions

    Science.gov (United States)

    Keller, Lindsay P.; McKeegan, K. D.; Sharp, Z. D.

    2012-01-01

    MIL 090001 is a large (>6 kg) carbonaceous chondrite that was classified as a member of the CV reduced subgroup (CVred) that was recovered during the 2009-2010 ANSMET field season [1]. Based on the abundance of refractory inclusions and the extent of aqueous alteration, Keller [2] suggested a CV2 classification. Here we report additional mineralogical and petrographic data for MIL 090001, its whole-rock oxygen isotopic composition and ion microprobe analyses of individual phases. The whole rock oxygen isotopic analyses show that MIL 090001 should be classified as a CR chondrite.

  17. Isotopic composition of neon in the galactic cosmic rays: a high resolution measurement

    International Nuclear Information System (INIS)

    Greiner, D.E.; Wiedenbeck, M.E.; Bieser, F.S.; Crawford, H.J.; Heckman, H.H.; Lindstrom, P.J.

    1979-06-01

    A measurement of the isotopic composition of galactic cosmic ray neon in the energy range 70 to 260 MeV/amu has been made using the U.C. Berkeley HKH instrument aboard ISEE-3. A combination of high resolution and good statistical accuracy makes possible a precise determination of the local interplanetary neon composition. We find 22 Ne/ 20 Ne = 0.64 +- 0.07 and 21 Ne/ 20 Ne < 0.30 in local interplanetary space. These ratios, when interpreted in using standard galactic propagation and solar modulation models, yield cosmic ray source abundances which are inconsistent with a solar-like source composition

  18. Mapping Precipitation Patterns from the Stable Isotopic Composition of Surface Waters: Olympic Peninsula, Washington State

    Science.gov (United States)

    Anders, A. M.; Brandon, M. T.

    2008-12-01

    Available data indicate that large and persistent precipitation gradients are tied to topography at scales down to a few kilometers, but precipitation patterns in the majority of mountain ranges are poorly constrained at scales less than tens of kilometers. A lack of knowledge of precipitation patterns hampers efforts to understand the processes of orographic precipitation and identify the relationships between geomorphic evolution and climate. A new method for mapping precipitation using the stable isotopic composition of surface waters is tested in the Olympic Mountains of Washington State. Measured δD and δ18O of 97 samples of surface water are linearly related and nearly inseparable from the global meteoric water line. A linear orographic precipitation model extended to include in effects of isotopic fractionation via Rayleigh distillation predicts precipitation patterns and isotopic composition of surface water. Seven parameters relating to the climate and isotopic composition of source water are used. A constrained random search identifies the best-fitting parameter set. Confidence intervals for parameter values are defined and precipitation patterns are determined. Average errors for the best-fitting model are 4.8 permil in δD. The difference between the best fitting model and other models within the 95% confidence interval was less than 20%. An independent high-resolution precipitation climatology documents precipitation gradients similar in shape and magnitude to the model derived from surface water isotopic composition. This technique could be extended to other mountain ranges, providing an economical and fast assessment of precipitation patterns requiring minimal field work.

  19. Finite Element Analysis of Composite Aircraft Fuselage Frame

    Science.gov (United States)

    Dandekar, Aditya Milind

    Composites have been introduced in aircraft industries, for their stronger, stiffer, and lighter properties than their metal-alloys counterparts. The general purpose of an aircraft is to transport commercial or military payload. Aircraft frames primarily maintains the shape of fuselage and prevent instability of the structure. Fuselage is similar as wing in construction which consist of longitudinal elements (longerons and stringers), transverse elements (frames and bulkheads) and its external skin. The fuselage is subjected to forces such as the wing reactions, landing gear reaction, empennage reaction, inertia forces subjected due to size and weight, internal pressure forces due to high altitude. Frames also ensure fail-safe design against skin crack propagation due to hoops stress. Ideal fuselage frames cross section is often circular ring shape with a frame cap of Z section. They are mainly made up of light alloy commonly used is aluminium alloys such as Al-2024, Al-7010, Al-7050, Al-7175. Aluminium alloys have good strength to density ratios in compression and bending of thin plate. A high strength to weight ratio of composite materials can result in a lighter aircraft structure or better safety factor. This research focuses on analysis of fuselage frame under dynamic load condition with change in material. Composites like carbon fibre reinforced plastics [CFRP] and glass fibre reinforced plastics [GFRP] are compared with traditional aluminium alloy Al-7075. The frame is subjected to impact test by dropping it at a velocity of 30 ft. / secs from a height of 86 inch from its centre of gravity. These parameters are considered in event of failure of landing gear, and an aircraft is subject to belly landing or gear-up landing. The shear flow is calculated due to impact force which acts in radial direction. The frame is analysed under static structural and explicit dynamic load conditions. Geometry is created in ANSYS Design Modeler. Analysis setup is created using

  20. Rare earth element and neodymium isotope tracing of element input and past ocean circulation. Study from north and south pacific seawater and sediments

    Energy Technology Data Exchange (ETDEWEB)

    Froellje, Henning

    2016-08-09

    Ocean circulation and cycling of trace elements within the oceanic water column is of great significance for modern and past climates. The global overturning circulation is responsible for the distribution of water masses, heat and particulate and dissolved compounds, while biological and chemical processes, such as primary productivity or particle scavenging, control the cycling of nutrients and trace elements in the ocean, and ultimately influence the ocean-atmosphere exchange of carbon. Rare earth elements (REE) and neodymium (Nd) isotopes are widely used as tracers for lithogenic element fluxes and modern and past ocean circulation and water mass mixing. The use of Nd isotopes in paleoceanographic investigations is based on the precise knowledge of processes involved in REE cycling and of the modern oceanic Nd isotope distribution. The Pacific is the largest of the world oceans, but it is highly underrepresented in present-day and past seawater Nd isotope and REE investigations compared to the Atlantic Ocean. In this study, Nd isotopes and REEs are analysed in North Pacific seawater (chapter 2) and sediment samples from the South Pacific (chapters 3-5) to contribute to a better understanding of sources and cycling of REEs and Nd isotopes in present-day seawater and to investigate past water mass mixing and circulation changes during the last glacial termination and throughout the last glacial-interglacial cycle. Neodymium isotopes in seawater and sedimentary archives (fossil fish teeth and debris, foraminifera, ferromanganese oxides, lithogenic particles) were analysed using multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS), and REE concentrations were analysed using isotope dilution ICP-MS. Results from combined analysis of REEs, and Nd and radium isotopes from North Pacific seawater (coastal seawaters of the Hawaiian Island of Oahu and seawater from the offshore Hawaii Ocean Time-series Station ALOHA) show a clear influence of the