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)

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.

The ground state infrared spectra of several isotopic forms of the CdH and ZnH radicals

International Nuclear Information System (INIS)

Urban, R.; Magg, U.; Birk, H.; Jones, H.

1990-01-01

The infrared spectra of six isotopic forms of cadmium monohydride, [ 116 CdH (7.6%), 114 CdH (28.9%), 113 CdH (12.3%), 112 CdH (24.1%), 111 CdH (12.7%), and 110 CdH (12.4%)] and four isotopic forms of zinc hydride [ 68 ZnH (18.6%), 67 ZnH (4.1%), 66 ZnH (27.8%), and 64 ZnH (48.9%)] have been observed in natural abundance in their ground electronic state ( 2 Σ + ) in the gas phase using a diode laser spectrometer. A number of transitions of 108 CdH (0.9%) and 106 CdH (1.2%) and 70 ZnH (0.6%) were also observed, but too little data was accumulated to allow a good analysis. The hydrides were produced by reaction of hydrogen with metal vapor at elevated temperature in an electric discharge. The analysis of the experimental data was carried out in two ways. (a) A complete set of Dunham parameters and spin--rotation parameters (γ parameters) was determined for each isotopic species of the two radicals and (b) a set of mass-independent parameters were calculated for both ZnH and CdH. Since only information over the isotopic species of the heavy atom was produced in each case, effects arising from a breakdown of the Born--Oppenheimer approximation were negligible. The effects of the strong anharmonicity present in these two molecules on the values of the parameters are discussed

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)

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.

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)

Assessment of phyto-available cadmium in soils using isotopic methods

International Nuclear Information System (INIS)

Gerard, Emilie

2000-01-01

The quantification of phyto-available Cd in soils is necessary to determine the transfer risk of this toxic element to plants. Isotopic methods (isotopic exchange kinetics (IEK), isotopic dilution) were used to characterize the phyto-available Cd and, practically, to select chemical methods for determining available Cd to plants. Rye grass (Lolium perenne L.), lettuce (Lactuca saliva L.) and the Cd hyper-accumulator Thlaspi caerulescens J. Presl. and C. Presl. were selected as test plants because of their wide range of Cd uptake ability. The chosen soils had different pH and displayed a Cd-contamination gradient due the atmospheric deposition of industrial particles. In the acidic soil, plants had access to the same metal pool, the one that was isotopically exchangeable with Cd 2+ . This was also the case for rye grass on the calcareous Soils but there, lettuce and T. caerulescens accessed a bigger and non-isotopically exchangeable pool that accounted for 16 to 52 % of the plant available Cd. Most of the Cd was isotopically exchangeable in a short time in the acidic soil (87 % within 21 days). In the calcareous soils two pools were identified, one pool was isotopically exchangeable in a very short time, and the other one Was not exchangeable after 21 days (21 to 10 % of the total Cd). Actually, the quantities of labile cd in the industrial particles which had contaminated these soils were very small. IEK methods and the measurement of the isotopic composition of Cd 2+ in soil solutions allowed for the estimation of the phyto-available Cd in soils, but cannot he commonly used. Most of the chemical extractants studied such as CaCl 2 or DTP A are suitable to assess the phyto-available Cd. However, on calcareous soils, the choice of extractant needs to sometimes be modified in relation to the rate of Cd plant absorption. (author) [fr

Quantifying the signature of the industrial revolution from Pb and Cd isotopes in the Susquehanna Shale Hills Critical Zone Observatory

Science.gov (United States)

Ma, L.; Herndon, E.; Jin, L.; Sanchez, D.; Brantley, S. L.

2013-12-01

Anthropogenic forcings have dominated metal cycling in many environments. During the period of the industrial revolution, mining and smelting of ores and combustion of fossil fuels released non-negligible amounts of potentially toxic metals such as Pb, Cd, Mn, and Zn into the environment. The extent and fate of these metal depositions in soils during that period however, have not been adequately evaluated. Here, we combine Pb isotopes with Cd isotopes to trace the sources of metal pollutants in a small temperate watershed (Shale Hills) in Pennsylvania. Previous work has shown that Mn additions to soils in central PA was caused by early iron production, as well as coal burning and steel making upwind. Comparison of the Pb and Cd concentrations in the bedrock and soils from this watershed show that Pb and Cd in soils at Shale Hills are best characterized by addition profiles, consistent with atmospheric additions. Three soil profiles at Shale Hills on the same hillslope have very similar anthropogenic Pb inventories. Pb isotope results further reveal that the extensive use of local coals during iron production in early 19th century in Pennsylvania is most likely the anthropogenic Pb source for the surface soils at Shale Hills. Pb concentrations and isotope ratios were used to calculate mass balance and diffusive transport models in soil profiles. The model results further reveal that during the 1850s to 1920s, coal burning in local iron blasting furnaces significantly increased the Pb deposition rates to 8-14 μg cm-2 yr-1, even more than modern Pb deposition rates derived from the use of leaded gasoline in the 1940s to 1980s. Furthermore, Cd has a low boiling point (~760 °C) and easily evaporates and condenses. The evaporation and condensation processes could generate systematic mass-dependent isotope fractionation between Cd in coal burning products and the naturally occurring Cd in the sulfide minerals of coals. This fractionation indicates that Cd isotopes can

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...

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.

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.

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

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

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

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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

The quadrupole moments of Cd and Zn isotopes - an apology

Science.gov (United States)

Haas, H.; Barbosa, M. B.; Correia, J. G.

2016-12-01

In 2010 we presented an update of the nuclear quadrupole moments (Q) for the Cd and Zn isotopes, based essentially on straightforward density functional (DF) calculations (H. Haas and J.G. Correia, Hyperfine Interact 198, 133-137 (2010)). It has been apparent for some years that the standard DF procedure obviously fails, however, to reproduce the known electric-field gradient (EFG) for various systems, typical cases being Cu2O, As and Sb, and the solid halogens. Recently a cure for this deficiency has been found in the hybrid DF technique. This method is now applied to solid Cd and Zn, and the resultant quadrupole moments are about 15 % smaller than in our earlier report. Also nuclear systematics, using the recently revised values of Q for the long-lived 11/2 isomers in111Cd to129Cd, together with earlier PAD data for107,109Cd, leads to the same conclusion. In addition, EFG calculations for the cadmium dimethyl molecule further support the new values: Q(111Cd, 5/2+) = .683(20) b, Q(67Zn, gs) = .132(5) b. This implies, that the value for the atomic EFG in the 3it {P}1 state of Zn must be revised, as it has been for Cd.

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.

Structure and optical properties of GaSe-CdSe composites driven by Cd intercalation in GaSe lamellar crystals

International Nuclear Information System (INIS)

Caraman, Iuliana; Kantser, Valeriu; Evtodiev, Igor; Untila, Dumitru; Dmitroglo, Liliana; Leontie, Liviu; Arzumanyan, Grigory

2015-01-01

A new composite material composed of GaSe and CdSe has been obtained by treatment of GaSe single-crystal lamellas in Cd vapors at temperatures of 773-853 K and intercalation of Cd interlayers. The structure and optical properties of the GaSe-CdSe composite material have been studied. The content of CdSe crystallites was found to grow with increasing treatment temperature or with increasing duration of treatment at a constant temperature. Analysis of XRD, PL, XPS, AFM, and Raman patterns has shown that the heterogeneous composite composed of micro and nanocrystallites of CdSe in GaSe can be obtained by Cd intercalation in a temperature range of 753-853 K. On the basis of Raman spectrum, the vibrational modes of the composite have been identified. The PL of these materials contains emission bands of free and bound excitons, donor-acceptor bands, and bands of recombination via impurity levels. The PL emission spectra measured at a temperature of 78 and 300 K for the composites result from the overlapping of the emission bands of the components of GaSe doped with Cd and the CdSe crystallites. (authors)

Characteristics of stable carbon isotopic composition of shale gas

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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.

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.

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 �

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.

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.

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.

Enhanced photoelectrochemical perporties of graphene nanowalls–CdS composite materials

International Nuclear Information System (INIS)

Song, Xuefen; Wang, Mingjun; Wei, Dapeng; Liu, Dun; Shi, Haofei; Hu, Chenguo; Fang, Liang; Zhang, Wei; Du, Chunlei

2015-01-01

A photo-electrochemical electrode of CdS–modified graphene walls (GWs) is fabricated via a successive ionic layer adsorption and reaction (SILAR) process. The as-prepared CdS–GWs composite structures could notably enhance photon absorption (in the visible region) and effectively facilitate the spatial separation of photo-generated carriers, bringing the enhanced photocurrent response. The effective area between CdS nanoparticles (NPs) and GWs is a crucial factor for the photocurrent density. Remarkably, the proposed CdS–GWs photo-anode displays satisfactory performance with the excellent photo-current density of 470 μA/cm 2 and wonderful stability as long as dozens of days. Our studies confirm that CdS–GWs nano-composites could work as high-performance photo-electrochemical electrodes for a lot of potential applications. - Highlights: • The GWs/CdS composites were synthesized via a simple SILAR process. • The mechanism of enhanced photocurrent response was investigated. • The GWs/CdS anode exhibits photo-current density of 470 μA/cm 2 . • The GWs/CdS anode has excellent stability.

Synthesis and photocatalytic activity of three-dimensional ZnS/CdS composites

International Nuclear Information System (INIS)

Liu, Shuling; Li, Honglin; Yan, Lu

2013-01-01

Graphical abstract: - Highlights: • 3D urchin-like ZnS/CdS composites were synthesized via a two-step method. • The CdS nanoparticles were assembled on the thorns of 3D ZnS urchins. • The ZnS/CdS composites show excellent photocatalytic degradation activities. • The modification of CdS on ZnS is responsible for the enhanced property. - Abstract: Urchin-like ZnS/CdS semiconductor composites were successfully synthesized by combining solvothermal route with homogeneous precipitation process. The as-obtained samples were characterized by means of XRD, EDX, TEM, HR-TEM, ED and FE-SEM techniques. The results show that the as-obtained composites were comprised of the hexagonal structure ZnS and CdS, and CdS nanoparticles were assembled on the surfaces of the thorns of urchin-like ZnS. In addition, the optical properties and photocatalytic activities of the as-prepared ZnS/CdS composites toward some organic dyes (such as Methyl Orange, Pyronine B, Rhodamine B and Methylene Blue) were separately investigated. It is found that the ZnS/CdS composites exhibit excellent photocatalytic degradation activity for these dyes under UV irradiation, as compared to corresponding pure ZnS urchins and commercial anatase TiO 2 (P-25). This enhanced activity may be related to the modification of CdS nanoparticles on the surfaces of thorns of ZnS urchins and a tentative mechanism for the enhanced photocatalytic degradation activities of the ZnS/CdS composite catalyst was proposed

Binding of Cd by ferrihydrite organo-mineral composites: Implications for Cd mobility and fate in natural and contaminated environments.

Science.gov (United States)

Du, Huihui; Peacock, Caroline L; Chen, Wenli; Huang, Qiaoyun

2018-09-01

Adsorption and coprecipitation of organic matter with iron (hydr)oxides can alter iron (hydr)oxide surface properties and their reactivity towards nutrient elements and heavy metals. Organo-mineral composites were synthesized using humic acid (HA) and iron oxide, during coprecipitation with ferrihydrite (Fh) and adsorption to pre-formed Fh with two C loadings. The Fh-HA coprecipitated composites have a higher C content and smaller surface area compared to the equivalent adsorbed composites. NanoSIMS shows there is a high degree of spatial correlation between Fe and C for both composites, but C distribution is more uniform in the coprecipitated composites. The C 1s NEXAFS reveals a similar C composition between the Fh-HA coprecipitated and adsorbed composites. However composites at high carbon loading are more enriched in aromatic C, likely due to preferential binding of carboxyl functional groups on aromatic rings in the HA. The amount of Cd sorbed is independent of the composite type, either coprecipitated or adsorbed, but is a function of the C loading. Composites with low C loading show Cd sorption that is almost identical to pure Fh, while composites with high C loading show Cd sorption that is intermediate between pure Fh and pure HA, with sorption significantly enhanced over pure Fh at pH < 6.5. A bidentate edge-sharing binding was identified for Cd on pure Fh and Cd-carboxyl binding on pure HA. These findings have significant implications not only for the sequestration of Cd in contaminated environments but also the coupled biogeochemical cycling of Cd, Fe and C in the critical zone. Crown Copyright © 2018. Published by Elsevier Ltd. All rights reserved.

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

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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.

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.)

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

Probing the collectivity in neutron-rich Cd isotopes via γ-ray spectroscopy

International Nuclear Information System (INIS)

Naqvi, Farheen

2011-01-01

The spin and configurational structure of excited states of 127 Cd, 125 Cd and 129 Cd, having two proton and three, five and one neutron holes, respectively in the doubly magic 132 Sn core have been studied. The isomeric states in Cd isotopes were populated in the fragmentation of a 136 Xe beam at an energy of 750 MeV/u on a 9 Be target of 4 g/cm 2 . The experiment was performed at GSI Darmstadt. The neutron-rich Cd isotopes were selected using the Bρ - ΔE - Bρ method at the FRagment Separator (FRS). Event by event identification of fragments in terms of their A (mass) and Z (charge) was provided by the standard FRS detectors. The reaction residues were implanted in a plastic stopper surrounded by 15 Ge cluster detectors from the RISING array to detect the γ decays. In 127 Cd, an isomeric state with a half-life of 17.5(3) μs has been detected. This yrast (19/2) + isomer is proposed to have mixed proton-neutron configurations and to decay by two competing stretched M2 and E3 transitions. Experimental results are compared with the isotone 129 Sn. In 125 Cd, apart from the previously observed (19/2) + isomer, two new metastable states at 3896 keV and 2141 keV have been detected. A half-life of 13.6(2) μs was measured for the (19/2) + isomer, having a decay structure similar to the corresponding isomeric state in 127 Cd. The higher lying isomers have a half-life of 3.1(1) μs and 2.5(15) ns, respectively. Time distributions of delayed γ transitions and γγ-coincidence relations were exploited to construct decay schemes for the two nuclei. Comparison of the experimental data with shell-model calculations is also discussed. The new information provides input for the proton-neutron interaction in nuclei around the doubly magic 132 Sn core. The γ decays of the isomeric states in 129 Cd were not observed experimentally. The reasons for the non-observation of delayed γ rays for 129 Cd are either an isomeric half-life of less than 93 ns based on the experimentally

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.

Cadmium isotope fractionation of materials derived from various industrial processes

Energy Technology Data Exchange (ETDEWEB)

Martinková, Eva, E-mail: eva.cadkova@geology.cz [Czech Geological Survey, Geologická 6, 152 00 Prague 5 (Czech Republic); Chrastný, Vladislav, E-mail: chrastny@fzp.czu.cz [Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, 165 21 Prague 6 (Czech Republic); Francová, Michaela, E-mail: michaela.francova@fzp.czu.cz [Faculty of Environmental Sciences, Czech University of Life Sciences Prague, Kamýcká 129, 165 21 Prague 6 (Czech Republic); Šípková, Adéla, E-mail: adela.sipkova@geology.cz [Czech Geological Survey, Geologická 6, 152 00 Prague 5 (Czech Republic); Čuřík, Jan, E-mail: jan.curik@geology.cz [Czech Geological Survey, Geologická 6, 152 00 Prague 5 (Czech Republic); Myška, Oldřich, E-mail: oldrich.myska@geology.cz [Czech Geological Survey, Geologická 6, 152 00 Prague 5 (Czech Republic); Mižič, Lukáš, E-mail: lukas.mizic@geology.cz [Czech Geological Survey, Geologická 6, 152 00 Prague 5 (Czech Republic)

2016-01-25

Highlights: • All studied industrial processes were accompanied by Cd isotope fractionation. • ϵ{sup 114/110} Cd values of the waste materials were discernible from primary sources. • Technology in use plays an important role in Cd isotope fractionation. - Abstract: Our study represents ϵ{sup 114/110} Cd {sub NIST3108} values of materials resulting from anthropogenic activities such as coal burning, smelting, refining, metal coating, and the glass industry. Additionally, primary sources (ore samples, pigment, coal) processed in the industrial premises were studied. Two sphalerites, galena, coal and pigment samples exhibited ϵ{sup 114/110} Cd{sub NIST3108} values of 1.0 ± 0.2, 0.2 ± 0.2, 1.3 ± 0.1, −2.3 ± 0.2 and −0.1 ± 0.3, respectively. In general, all studied industrial processes were accompanied by Cd isotope fractionation. Most of the industrial materials studied were clearly distinguishable from the samples used as a primary source based on ϵ{sup 114/110} Cd {sub NIST3108} values. The heaviest ϵ{sup 114/110} Cd{sub NIST3108} value of 58.6 ± 0.9 was found for slag resulting from coal combustion, and the lightest ϵ{sup 114/110} Cd{sub NIST3108} value of −23 ± 2.5 was observed for waste material after Pb refinement. It is evident that ϵ{sup 114/110} Cd {sub NIST3108} values depend on technological processes, and in case of incomplete Cd transfer from source to final waste material, every industrial activity creates differences in Cd isotope composition. Our results show that Cd isotope analysis is a promising tool to track the origins of industrial waste products.

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

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.

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)

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.

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

CD19 CAR-T cells of defined CD4+:CD8+ composition in adult B cell ALL patients.

Science.gov (United States)

Turtle, Cameron J; Hanafi, Laïla-Aïcha; Berger, Carolina; Gooley, Theodore A; Cherian, Sindhu; Hudecek, Michael; Sommermeyer, Daniel; Melville, Katherine; Pender, Barbara; Budiarto, Tanya M; Robinson, Emily; Steevens, Natalia N; Chaney, Colette; Soma, Lorinda; Chen, Xueyan; Yeung, Cecilia; Wood, Brent; Li, Daniel; Cao, Jianhong; Heimfeld, Shelly; Jensen, Michael C; Riddell, Stanley R; Maloney, David G

2016-06-01

T cells that have been modified to express a CD19-specific chimeric antigen receptor (CAR) have antitumor activity in B cell malignancies; however, identification of the factors that determine toxicity and efficacy of these T cells has been challenging in prior studies in which phenotypically heterogeneous CAR-T cell products were prepared from unselected T cells. We conducted a clinical trial to evaluate CD19 CAR-T cells that were manufactured from defined CD4+ and CD8+ T cell subsets and administered in a defined CD4+:CD8+ composition to adults with B cell acute lymphoblastic leukemia after lymphodepletion chemotherapy. The defined composition product was remarkably potent, as 27 of 29 patients (93%) achieved BM remission, as determined by flow cytometry. We established that high CAR-T cell doses and tumor burden increase the risks of severe cytokine release syndrome and neurotoxicity. Moreover, we identified serum biomarkers that allow testing of early intervention strategies in patients at the highest risk of toxicity. Risk-stratified CAR-T cell dosing based on BM disease burden decreased toxicity. CD8+ T cell-mediated anti-CAR transgene product immune responses developed after CAR-T cell infusion in some patients, limited CAR-T cell persistence, and increased relapse risk. Addition of fludarabine to the lymphodepletion regimen improved CAR-T cell persistence and disease-free survival. Immunotherapy with a CAR-T cell product of defined composition enabled identification of factors that correlated with CAR-T cell expansion, persistence, and toxicity and facilitated design of lymphodepletion and CAR-T cell dosing strategies that mitigated toxicity and improved disease-free survival. ClinicalTrials.gov NCT01865617. R01-CA136551; Life Science Development Fund; Juno Therapeutics; Bezos Family Foundation.

CD19 CAR–T cells of defined CD4+:CD8+ composition in adult B cell ALL patients

Science.gov (United States)

Turtle, Cameron J.; Hanafi, Laïla-Aïcha; Berger, Carolina; Gooley, Theodore A.; Cherian, Sindhu; Hudecek, Michael; Sommermeyer, Daniel; Melville, Katherine; Pender, Barbara; Budiarto, Tanya M.; Robinson, Emily; Steevens, Natalia N.; Chaney, Colette; Soma, Lorinda; Chen, Xueyan; Li, Daniel; Cao, Jianhong; Heimfeld, Shelly; Jensen, Michael C.; Riddell, Stanley R.; Maloney, David G.

2016-01-01

BACKGROUND. T cells that have been modified to express a CD19-specific chimeric antigen receptor (CAR) have antitumor activity in B cell malignancies; however, identification of the factors that determine toxicity and efficacy of these T cells has been challenging in prior studies in which phenotypically heterogeneous CAR–T cell products were prepared from unselected T cells. METHODS. We conducted a clinical trial to evaluate CD19 CAR–T cells that were manufactured from defined CD4+ and CD8+ T cell subsets and administered in a defined CD4+:CD8+ composition to adults with B cell acute lymphoblastic leukemia after lymphodepletion chemotherapy. RESULTS. The defined composition product was remarkably potent, as 27 of 29 patients (93%) achieved BM remission, as determined by flow cytometry. We established that high CAR–T cell doses and tumor burden increase the risks of severe cytokine release syndrome and neurotoxicity. Moreover, we identified serum biomarkers that allow testing of early intervention strategies in patients at the highest risk of toxicity. Risk-stratified CAR–T cell dosing based on BM disease burden decreased toxicity. CD8+ T cell–mediated anti-CAR transgene product immune responses developed after CAR–T cell infusion in some patients, limited CAR–T cell persistence, and increased relapse risk. Addition of fludarabine to the lymphodepletion regimen improved CAR–T cell persistence and disease-free survival. CONCLUSION. Immunotherapy with a CAR–T cell product of defined composition enabled identification of factors that correlated with CAR–T cell expansion, persistence, and toxicity and facilitated design of lymphodepletion and CAR–T cell dosing strategies that mitigated toxicity and improved disease-free survival. TRIAL REGISTRATION. ClinicalTrials.gov NCT01865617. FUNDING. R01-CA136551; Life Science Development Fund; Juno Therapeutics; Bezos Family Foundation. PMID:27111235

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.

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.

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.

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.

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.

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.

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

Heavy metal and Pb isotopic compositions of aquatic organisms in the Pearl River Estuary, South China

International Nuclear Information System (INIS)

Ip, C.C.M.; Li, X.D.; Zhang, G.; Wong, C.S.C.; Zhang, W.L.

2005-01-01

The accumulation of trace metals in aquatic organisms may lead to serious health problems through the food chain. The present research project aims to study the accumulation and potential sources of trace metals in aquatic organisms of the Pearl River Estuary (PRE). Four groups of aquatic organisms, including fish, crab, shrimp, and shellfish, were collected in the PRE for trace metal and Pb isotopic analyses. The trace metal concentrations in the aquatic organism samples ranged from 0.01 to 2.10 mg/kg Cd, 0.02 to 4.33 mg/kg Co, 0.08 to 4.27 mg/kg Cr, 0.15 to 77.8 mg/kg Cu, 0.17 to 31.0 mg/kg Ni, 0.04 to 30.7 mg/kg Pb, and 8.78 to 86.3 mg/kg Zn (wet weight). High concentrations of Cd were found in crab, shrimp and shellfish samples, while high concentration of Pb was found in fish. In comparison with the baseline reference values in other parts of the world, fish in the PRE had the highest elevated trace metals. The results of Pb isotopic compositions indicated that the bioaccumulation of Pb in fish come from a wide variety of food sources and/or exposure pathways, particularly the anthropogenic inputs. - Relative high concentrations of Cd were found in crab, shrimp and shellfish samples while high concentration of Pb was found in fish, particularly from the anthropogenic inputs

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)

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.

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.

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 ...

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...

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.

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...

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

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.

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.)

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

Background analysis for the beta-spectrum of the isotope 113Cd in the COBRA experiment

Energy Technology Data Exchange (ETDEWEB)

Platzek, Stephan [Technische Universitaet Dresden (Germany); Collaboration: COBRA-Collaboration

2016-07-01

The COBRA experiment uses Cadmium-Zinc-Telluride as detector material. This semiconductor contains several isotopes that are candidates for neutrinoless double beta-decay. Due to the natural abundance of the detector material various other isotopes are present as well. One of them is {sup 113}Cd with an abundance of about 12%. The fourfold forbidden non-unique beta-decay of {sup 113}Cd is a rare process with a half-life of about 8.10{sup 15} years. The shape of the spectrum is still topic of scientific discussions because of various forecasts given by theoretical models. The signal related to this decay is by far the most prominent in the COBRA setup causing more than 98% of the total rate. In this talk potential background components contributing to the {sup 113}Cd beta-spectrum are discussed with the aim to develop a detailed background simulation with the program VENOM (based on Geant4), that includes background sources originating from cosmic activation as well as natural radioactivity and detector specific effects.

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.

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)

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

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

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.

The neodymium stable isotope composition of the silicate Earth and chondrites

Science.gov (United States)

McCoy-West, Alex J.; Millet, Marc-Alban; Burton, Kevin W.

2017-12-01

The non-chondritic neodymium (Nd) 142Nd/144Nd ratio of the silicate Earth potentially provides a key constraint on the accretion and early evolution of the Earth. Yet, it is debated whether this offset is due to the Earth being formed from material enriched in s-process Nd isotopes or results from an early differentiation process such as the segregation of a late sulfide matte during core formation, collisional erosion or a some combination of these processes. Neodymium stable isotopes are potentially sensitive to early sulfide segregation into Earth's core, a process that cannot be resolved using their radiogenic counterparts. This study presents the first comprehensive Nd stable isotope data for chondritic meteorites and terrestrial rocks. Stable Nd measurements were made using a double spike technique coupled with thermal ionisation mass spectrometry. All three of the major classes of chondritic meteorites, carbonaceous, enstatite and ordinary chondrites have broadly similar isotopic compositions allowing calculation of a chondritic mean of δ146/144Nd = -0.025 ± 0.025‰ (±2 s.d.; n = 39). Enstatite chondrites yield the most uniform stable isotope composition (Δ146/144Nd = 26 ppm), with considerably more variability observed within ordinary (Δ146/144Nd = 72 ppm) and carbonaceous meteorites (Δ146/144Nd = 143 ppm). Terrestrial weathering, nucleosynthetic variations and parent body thermal metamorphism appear to have little measurable effect on δ146/144Nd in chondrites. The small variations observed between ordinary chondrite groups most likely reflect inherited compositional differences between parent bodies, with the larger variations observed in carbonaceous chondrites being linked to varying modal proportions of calcium-aluminium rich inclusions. The terrestrial samples analysed here include rocks ranging from basaltic to rhyolitic in composition, MORB glasses and residual mantle lithologies. All of these terrestrial rocks possess a broadly similar Nd

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

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)

Graphene oxide–CdS composite with high photocatalytic degradation and disinfection activities under visible light irradiation

Energy Technology Data Exchange (ETDEWEB)

Gao, Peng; Liu, Jincheng [School of Civil and Environmental Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); Sun, Darren Delai, E-mail: DDSUN@ntu.edu.sg [School of Civil and Environmental Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); Ng, Wunjern [School of Civil and Environmental Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore); Nanyang Environment and Water Research Institute, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore)

2013-04-15

Highlights: ► GO–CdS composites were prepared through a novel two-phase mixing method. ► Uniform deposition of CdS nanoparticles on GO sheets. ► Reduced charge recombination rate. ► Enhanced photo-stability. ► High photodegradation and disinfection efficiency. -- Abstract: Graphene oxide (GO)–CdS composites were synthesized via a novel two-phase mixing method successfully. CdS nanoparticles were uniformly self-assembled on GO sheets at water/toluene interface. The photocatalytic degradation (photodegradation) and disinfection activities of GO–CdS composites were investigated thoroughly. The results show that GO–CdS composites exhibit higher efficiency in photodegradation of various water pollutants than pure CdS nanoparticles under visible light irradiation. In addition, the interactions between GO sheets and CdS nanoparticles inhibit the photo-corrosion of CdS and leaching of Cd{sup 2+}. Only 3.5 wt% Cd{sup 2+} of GO–CdS was leached out after photodegradation, while 38.6 wt% Cd{sup 2+} of CdS was lost into aqueous solution. Furthermore, the disinfection activity of GO–CdS composites was investigated for the first time. Nearly 100% of both Gram-negative Escherichia coli (E. coli) and Gram-positive Bacillus subtilis (B. subtilis) were killed within 25 min under visible light irradiation. The excellent performances of GO–CdS composites can be attributed to that (1) effective charge transfer from CdS to GO reduces the recombination rate of photo-generated electron–hole pairs; (2) uniform deposition of CdS on GO sheets eliminates aggregation of CdS nanoparticles; and (3) the strong interactions between GO and CdS enhancing the durability of GO–CdS composites. Finally, the mechanism behind these excellent performances was verified by transient photocurrent measurement and further confirmed by ESR technique as well as employing a radical scavenging species – dimethyl sulfoxide (DMSO)

Graphene oxide–CdS composite with high photocatalytic degradation and disinfection activities under visible light irradiation

International Nuclear Information System (INIS)

Gao, Peng; Liu, Jincheng; Sun, Darren Delai; Ng, Wunjern

2013-01-01

Highlights: ► GO–CdS composites were prepared through a novel two-phase mixing method. ► Uniform deposition of CdS nanoparticles on GO sheets. ► Reduced charge recombination rate. ► Enhanced photo-stability. ► High photodegradation and disinfection efficiency. -- Abstract: Graphene oxide (GO)–CdS composites were synthesized via a novel two-phase mixing method successfully. CdS nanoparticles were uniformly self-assembled on GO sheets at water/toluene interface. The photocatalytic degradation (photodegradation) and disinfection activities of GO–CdS composites were investigated thoroughly. The results show that GO–CdS composites exhibit higher efficiency in photodegradation of various water pollutants than pure CdS nanoparticles under visible light irradiation. In addition, the interactions between GO sheets and CdS nanoparticles inhibit the photo-corrosion of CdS and leaching of Cd 2+ . Only 3.5 wt% Cd 2+ of GO–CdS was leached out after photodegradation, while 38.6 wt% Cd 2+ of CdS was lost into aqueous solution. Furthermore, the disinfection activity of GO–CdS composites was investigated for the first time. Nearly 100% of both Gram-negative Escherichia coli (E. coli) and Gram-positive Bacillus subtilis (B. subtilis) were killed within 25 min under visible light irradiation. The excellent performances of GO–CdS composites can be attributed to that (1) effective charge transfer from CdS to GO reduces the recombination rate of photo-generated electron–hole pairs; (2) uniform deposition of CdS on GO sheets eliminates aggregation of CdS nanoparticles; and (3) the strong interactions between GO and CdS enhancing the durability of GO–CdS composites. Finally, the mechanism behind these excellent performances was verified by transient photocurrent measurement and further confirmed by ESR technique as well as employing a radical scavenging species – dimethyl sulfoxide (DMSO)

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

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.

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

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.

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

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.

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.

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

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.

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.)

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

Spins, moments and radii of Cd isotopes

CERN Document Server

Hammen, Michael

The complex nature of the nucleon-nucleon interaction and the wide range of systems covered by the roughly 3000 known nuclides leads to a multitude of effects observed in nuclear structure. Among the most prominent ones is the occurence of shell closures at so-called ”magic numbers”, which are explained by the nuclear shell model. Although the shell model already is on duty for several decades, it is still constantly extended and improved. For this process of extension, fine adjustment and verification, it is important to have experimental data of nuclear properties, especially at crucial points like in the vicinity of shell closures. This is the motivation for the work performed in this thesis: the measurement and analysis of nuclear ground state properties of the isotopic chain of $^{100−130}$Cd by collinear laser spectroscopy. The experiment was conducted at ISOLDE/CERN using the collinear laser spectroscopy apparatus COLLAPS. This experiment is the continuation of a run on neutral atomic cadmium f...

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

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

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)

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

Composition and performance of thin film CdSe electrodeposited from selenosulfite solution

International Nuclear Information System (INIS)

Szabo, J.P.; Simms, D.; Cocivera, M.

1985-01-01

Cathodic electrodeposition of thin film CdSe from aqueous selenosulfite solution has been studied as function of solution composition and electrode potential. The Cd/Se ratio has been analyzed using polarography and Rutherford backscattering spectroscopy. Polarography gives a compostion averaged over the whole film (2cm 2 ) while RBS gives local surface composition (1 mm 2 ). The average Cd/Se ratio is 1.1, but some variation was found to occur across the surface of film (0.82 to 1.2)

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.

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)

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

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...

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...

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.)

Stable chromium isotopic composition of meteorites and metal-silicate experiments: Implications for fractionation during core formation

Science.gov (United States)

Bonnand, P.; Williams, H. M.; Parkinson, I. J.; Wood, B. J.; Halliday, A. N.

2016-02-01

We present new mass independent and mass dependent Cr isotope compositions for meteorites measured by double spike thermal ionisation mass spectrometry. Small differences in both mass independent 53Cr and 54Cr relative to the Bulk Silicate Earth are reported and are very similar to previously published values. Carbonaceous chondrites are characterised by an excess in 54Cr compared to ordinary and enstatite chondrites which make mass independent Cr isotopes a useful tool for distinguishing between meteoritic groups. Mass dependent stable Cr isotope compositions for the same samples are also reported. Carbonaceous and ordinary chondrites are identical within uncertainty with average δ53 Cr values of - 0.118 ± 0.040 ‰ and - 0.143 ± 0.074 ‰ respectively. The heaviest isotope compositions are recorded by an enstatite chondrite and a CO carbonaceous chondrite, both of which have relatively reduced chemical compositions implying some stable Cr isotope fractionation related to redox processes in the circumstellar disk. The average δ53 Cr values for chondrites are within error of the estimate for the Bulk Silicate Earth (BSE) also determined by double spiking. The lack of isotopic difference between chondritic material and the BSE provides evidence that Cr isotopes were not fractionated during core formation on Earth. A series of high-pressure experiments was also carried out to investigate stable Cr isotope fractionation between metal and silicate and no demonstrable fractionation was observed, consistent with our meteorites data. Mass dependent Cr isotope data for achondrites suggest that Cr isotopes are fractionated during magmatic differentiation and therefore further work is required to constrain the Cr isotopic compositions of the mantles of Vesta and Mars.

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.

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

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)

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

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

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

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.

Bioavailability and uptake of smelter emissions in freshwater zooplankton in northeastern Washington, USA lakes using Pb isotope analysis and trace metal concentrations.

Science.gov (United States)

Child, A W; Moore, B C; Vervoort, J D; Beutel, M W

2018-07-01

The upper Columbia River and associated valley systems are highly contaminated with metal wastes from nearby smelting operations in Trail, British Columbia, Canada (Teck smelter), and to a lesser extent, Northport, Washington, USA (Le Roi smelter). Previous studies have investigated depositional patterns of airborne emissions from these smelters, and documented the Teck smelter as the primary metal contamination source. However, there is limited research directed at whether these contaminants are bioavailable to aquatic organisms. This study investigates whether smelter derived contaminants are bioavailable to freshwater zooplankton. Trace metal (Zn, Cd, As, Sb, Pb and Hg) concentrations and Pb isotope compositions of zooplankton and sediment were measured in lakes ranging from 17 to 144 km downwind of the Teck smelter. Pb isotopic compositions of historic ores used by both smelters are uniquely less radiogenic than local geologic formations, so when zooplankton assimilate substantial amounts of smelter derived metals their compositions deviate from local baseline compositions toward ore compositions. Sediment metal concentrations and Pb isotope compositions in sediment follow significant (p < 0.001) negative exponential and sigmoidal patterns, respectively, as distance from the Teck smelting operation increases. Zooplankton As, Cd, and Sb contents were related to distance from the Teck smelter (p < 0.05), and zooplankton Pb isotope compositions suggest As, Cd, Sb and Pb from historic and current smelter emissions are biologically available to zooplankton. Zooplankton from lakes within 86 km of the Teck facility display isotopic evidence that legacy ore pollution is biologically available for assimilation. However, without water column data our study is unable to determine if legacy contaminants are remobilized from lake sediments, or erosional pathways from the watershed. Copyright © 2018 Elsevier Ltd. All rights reserved.

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

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.

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

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,.

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.

Stable isotope study of a new chondrichthyan fauna (Kimmeridgian, Porrentruy, Swiss Jura): an unusual freshwater-influenced isotopic composition for the hybodont shark Asteracanthus

Science.gov (United States)

Leuzinger, L.; Kocsis, L.; Billon-Bruyat, J.-P.; Spezzaferri, S.; Vennemann, T.

2015-12-01

Chondrichthyan teeth (sharks, rays, and chimaeras) are mineralized in isotopic equilibrium with the surrounding water, and parameters such as water temperature and salinity can be inferred from the oxygen isotopic composition (δ18Op) of their bioapatite. We analysed a new chondrichthyan assemblage, as well as teeth from bony fish (Pycnodontiformes). All specimens are from Kimmeridgian coastal marine deposits of the Swiss Jura (vicinity of Porrentruy, Ajoie district, NW Switzerland). While the overall faunal composition and the isotopic composition of bony fish are generally consistent with marine conditions, unusually low δ18Op values were measured for the hybodont shark Asteracanthus. These values are also lower compared to previously published data from older European Jurassic localities. Additional analyses on material from Solothurn (Kimmeridgian, NW Switzerland) also have comparable, low-18O isotopic compositions for Asteracanthus. The data are hence interpreted to represent a so far unique, freshwater-influenced isotopic composition for this shark that is classically considered a marine genus. While reproduction in freshwater or brackish realms is established for other hybodonts, a similar behaviour for Asteracanthus is proposed here. Regular excursions into lower salinity waters can be linked to the age of the deposits and correspond to an ecological adaptation, most likely driven by the Kimmeridgian transgression and by the competition of the hybodont shark Asteracanthus with the rapidly diversifying neoselachians (modern sharks).

Synthesis of CdS/ZnO/graphene composite with high-efficiency photoelectrochemical activities under solar radiation

International Nuclear Information System (INIS)

Han, Weijia; Ren, Long; Qi, Xiang; Liu, Yundan; Wei, Xiaolin; Huang, Zongyu; Zhong, Jianxin

2014-01-01

Graphical abstract: A graphene-based ternary composite was prepared by loading ZnO and CdS nanoparticles in graphene nanosheets via a facile one-pot hydrothermal process. The as-prepared ternary CdS/ZnO/graphene composite has shown excellent photoelectrochemical activity, which indicate that it may have a great potential application in photoelectrochemical hydrogen production from water reduction under sunlight. - Highlights: • A graphene-based ternary composite was prepared by loading ZnO and CdS nanoparticles in graphene nanosheets via a facile one-step hydrothermal method. • The CdS/ZnO/graphene composite demonstrated improved light-harvesting and superior durability photoelectrochemical activity. • The ternary composite can hinder the recombination of photo electrons and holes and improve charge transfer to enhance the photocatalytic activity. - Abstract: A novel ternary CdS/ZnO/graphene composite has been successfully prepared by loading ZnO and CdS nanoparticles in graphene nanosheets via a facile one-step hydrothermal method. The microstructures and properties have been examined by X-ray diffraction (XRD), scanning electron microscopy with an energy dispersive spectroscope (EDS), transmission electron microscopy, Raman and UV–vis diffuse reflectance spectra (DRS). The characterization results reveal that the crystalline of the composite is very well, the graphene sheets were tightly coated with ZnO and CdS nanoparticles, and the light-harvesting was effectively strengthened. Taking photoelectrochemical test, the ternary CdS/ZnO/graphene composite exhibits enhanced photocatalytic activity compared with its foundation matrix binary composites and pure ZnO and CdS. The improved photocatalytic performance can be attributed to the enhanced light absorption, the extremely efficient charge separation, as well as superior durability of the ternary composite. It is proposed that graphene-based composites by coupling graphene to suitable, multiple

Distinguishing ectomycorrhizal and saprophytic fungi using carbon and nitrogen isotopic compositions

Directory of Open Access Journals (Sweden)

Weiguo Hou

2012-05-01

Full Text Available Ectomycorrhizal fungi, a group of widespread symbiotic fungi with plant, obtain carbon source from trees and improve plant mineral nutrient uptake with their widespread hyphal network. Ectomycorrhizal fungi can be used as inoculants to improve the survival rates of plantation. Saprophytic fungi use the nutrition from the debris of plant or animals, and it is difficult to distinguish the saprophytic and ectomycorrhizal fungi by morphological and anatomic methods. In this research, the differences of stable carbon and nitrogen isotopic compositions of these fungi were analyzed. The results showed that the abundances of 13C of were higher than those of ectomycorrhizal fungi and the abundances of 15N of saprophytic fungi were lower than those of ectomycorrhizal fungi. Such differences of stable carbon and nitrogen isotopic compositions between ectomycorrhizal fungi and saprophytic fungi can be ascribed to their different nutrition sources and ecological functions. These results collectively indicate that stable carbon and nitrogen isotopic compositions are an effective proxy for distinguishing between ectomycorrhizal and saprophytic fungi.

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 �

Predicting the solubility and lability of Zn, Cd, and Pb in soils from a minespoil-contaminated catchment by stable isotopic exchange

Science.gov (United States)

Marzouk, E. R.; Chenery, S. R.; Young, S. D.

2013-12-01

The Rookhope catchment of Weardale, England, has a diverse legacy of contaminated soils due to extensive lead mining activity over four centuries. We measured the isotopically exchangeable content of Pb, Cd and Zn (E-values) in a large representative subset of the catchment soils (n = 246) using stable isotope dilution. All three metals displayed a wide range of %E-values (c. 1-100%) but relative lability followed the sequence Cd > Pb > Zn. A refinement of the stable isotope dilution approach also enabled detection of non-reactive metal contained within suspended sub-micron (dilution, in a diverse range of soil ecosystems within the catchment of an old Pb/Zn mining area. Assess the controlling influences of soil properties on metal lability and develop predictive algorithms for metal lability in the contaminated catchment based on simple soil properties (such as pH, organic matter (LOI), and total metal content). Examine the incidence of non-isotopically-exchangeable metal held within suspended colloidal particles (SCP-metal) in filtered soil solutions (<0.22 μm) by comparing E-values from isotopic abundance in solutions equilibrated with soil and in a resin phase equilibrated with the separated solution. Assess the ability of a geochemical speciation model, WHAM(VII), to predict metal solubility using isotopically exchangeable metal as an input variable.

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.

Solution processable RGO-CdZnS composite for solar light responsive photocatalytic degradation of 4-Nitrophenol

Science.gov (United States)

Ibrahim, Sk; Chakraborty, Koushik; Pal, Tanusri; Ghosh, Surajit

2017-05-01

We report the one pot single step synthesis and characterization of solution processable reduced graphene oxide (RGO) - cadmium zinc sulfide (CdZnS) nanocomposite materials. The composite was characterized structurally and morphologically by XRD and TEM studies. The reduction of GO in RGO-CdZnS composite, was confirmed by XPS and Raman spectroscopy. The photocatalytic activity of the RGO-CdZnS composite was investigated towards the degradation of 4-Nitrophenol. A notable increase of photocatalytic efficiency of RGO-CdZnS compare to controlled CdZnS was observed. Here RGO plays a crucial role to efficient photo induced charge separation from the CdZnS, and decreases the electron-hole recombination probability and subsequently enhanced the photocatalytic activity of the RGO-CdZnS composite material under simulated solar light irradiation. This work highlights the potential application of RGO-based materials in the field of photocatalytic degradation of organic water pollutant.

Coulomb excitation of {sup 123}Cd

Energy Technology Data Exchange (ETDEWEB)

Hartig, Anna-Lena; Kroell, Thorsten; Ilieva, Stoyanka; Boenig, Sabine; Thuerauf, Michael [IKP, TU Darmstadt (Germany); Simpson, Gary; Drouet, Floriane; Ramdhane, Mourad [LPSC, Grenoble (France); Georgiev, Georgi [CSNSM, Orsay (France); Kesteloot, Nele; Wrzosek-Lipska, Kasia [KU, Leuven (Belgium); Jungclaus, Andrea; Illana Sison, Andres [CSIC, Madrid (Spain); Balabanski, Dimiter [INRNE-BAS, Sofia (Bulgaria); Warr, Nigel [Koeln Univ. (Germany). IKP; Voulot, Didier; Wenander, Fredrik; Marsh, Bruce [CERN, Geneva (Switzerland)

2013-07-01

On the neutron-rich side of the valley of stability in the vicinity of the double magic nucleus {sup 132}Sn one can find the {sup 123}Cd isotope. Surprisingly the neutron-rich even-A Cd isotopes in this region are showing signs of collectivity beyond that calculated by modern shell-model predictions. In order to gain a deeper insight in this phenomenon we started to extend these studies to odd-A Cd isotopes. As first isotope the exotic nucleus {sup 123}Cd was produced for safe Coulomb excitation by the ISOLDE facility at CERN and post-accelerated by REX-ISOLDE. The γ-decay from excited states was detected with the MINIBALL array. A report on the status of the ongoing analysis is given.

Pb-Zn-Cd-Hg multi isotopic characterization of the Loire River Basin, France

Science.gov (United States)

Millot, R.; Widory, D.; Innocent, C.; Guerrot, C.; Bourrain, X.; Johnson, T. M.

2012-12-01

The contribution of human activities such as industries, agriculture and domestic inputs, becomes more and more significant in the chemical composition (major ions and pollutants such as metals) of the dissolved load of rivers. Furthermore, this influence can also be evidenced in the suspended solid matter known to play an important role in the transport of heavy metals through river systems. Human factors act as a supplementary key process. Therefore the mass-balance for the budget of catchments and river basins include anthropogenic disturbances. The Loire River in central France is approximately 1010 km long and drains an area of 117,800 km2. Initially, the Loire upstream flows in a south to north direction originating in the Massif Central, and continues up to the city of Orléans, 650 km from the source. In the upper basin, the bedrock is old plutonic rock overlain by much younger volcanic rocks. The Loire River then follows a general east to west direction to the Atlantic Ocean. The intermediate basin includes three major tributaries flowing into the Loire River from the left bank: the Cher, the Indre and the Vienne rivers; the main stream flows westward and its valley stretches toward the Atlantic Ocean. Here, the Loire River drains the sedimentary series of the Paris Basin, mainly carbonate deposits. The lower Loire basin drains pre-Mesozoic basement of the Armorican Massif and its overlying Mesozoic to Cenozoic sedimentary deposits. The Loire River is one of the main European riverine inputs to the Atlantic ocean. Here we are reporting concentration and isotope data for heavy metals Zn-Cd-Pb-Hg in river waters and suspended sediments from the Loire River Basin. In addition, we also report concentration and isotope data for these metals for the different industrial sources within the Loire Basin, as well as data for biota samples such as mussels and oysters from the Bay of Biscay and North Brittany. These organisms are known to be natural accumulators of

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)

Polyaniline/carbon nanotube/CdS quantum dot composites with enhanced optical and electrical properties

Energy Technology Data Exchange (ETDEWEB)

Goswami, Mrinmoy [Department of Physics, National Institute of Technology, Durgapur, 713209 (India); Ghosh, Ranajit, E-mail: ghosh.ranajit@gmail.com [CSIR-Central Mechanical Engineering Research Institute, Durgapur, 713209 (India); Maruyama, Takahiro [Department of Applied Chemistry, Meijo University, Nagoya, 4688502 (Japan); Meikap, Ajit Kumar [Department of Physics, National Institute of Technology, Durgapur, 713209 (India)

2016-02-28

Graphical abstract: - Highlights: • A new kind of polyaniline/carbon nanotube/CdS quantum dot composites have been synthesized via in-situ polymerization of aniline monomer. • A degree of increase in conductivity. • Size-dependent optical properties of CdS quantum dots have been observed. - Abstract: A new kind of polyaniline/carbon nanotube/CdS quantum dot composites have been developed via in-situ polymerization of aniline monomer in the presence of dispersed CdS quantum dots (size: 2.7–4.8 nm) and multi-walled carbon nanotubes (CNT), which exhibits enhanced optical and electrical properties. The existences of 1st order, 2nd order, and 3rd order longitudinal optical phonon modes, strongly indicate the high quality of synthesized CdS quantum dots. The occurrence of red shift of free exciton energy in photoluminescence is due to size dependent quantum confinement effect of CdS. The conductivity of the composites (for example PANI/CNT/CdS (2 wt.% CdS)) is increased by about 7 of magnitude compared to that of pure PANI indicating a charge transfer between CNT and polymer via CdS quantum dots. This advanced material has a great potential for high-performance of electro-optical applications.

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

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

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.

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

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

Isotopic and chemical characterization of coal in Pakistan

International Nuclear Information System (INIS)

Qureshi, R.M.; Hasany, S.M.; Javed, T.; Sajjad, M.I.; Shah, Z.; Rehman, H.

1993-11-01

Stable carbon isotope ratios (delta/sup 13/C PDB) and toxic/trace element concentration levels are determined for Tertiary coal samples collected from seven coal fields in Pakistan. No systematic isotope effects are found in the process of coal liquefaction from peat to Tertiary lignites and sub bituminous coal. Similarly, no age effects are observed during the Tertiary regime. The observed variations in the carbon isotopic composition of coal obtained from 'Sharigh coal field' and the 'Sor-Range/Degari coal field' in Baluchistan are attributed to the depositional environments. More sampling of stable carbon isotope analysis are required to validate these observations. Significant concentrations of toxic elements such as S, Cr, Cd and Pb in Makarwal coal may pose environmental and engineering/operational problems for thermal power plants. (author)

The Synthesis of Wavelength-Controlled CdTe/Hydroxyapatite Composites and Their Fluorescence Enhancement by Bovine Serum Albumin

Directory of Open Access Journals (Sweden)

Li Jin

2016-01-01

Full Text Available For the last ten years, quantum dots modified by biological materials have made it possible to study biochemical processes by means of biomedical imaging. This thesis introduced how the fluorescence CdTe quantum dots/hydroxyapatite composites were synthesized and how their structure, morphology, and fluorescence property were characterized by using TEM, XRD, EDS, UV-vis absorption spectra, and fluorescence spectra. The fluorescence spectra indicated the superb photometric characteristics of CdTe/HA composites. We also found that refluxing temperature and time had prominent effects on fluorescence wavelength and intensity of CdTe/HA composites, so the fluorescence emission wavelength of CdTe/HA composites could be controlled. In addition, the effect of BSA on the fluorescence properties of CdTe/HA composites was studied. The fluorescent emission intensity of CdTe/HA composites was enhanced directly with increasing concentrations of BSA; meanwhile, the fluorescence emission intensity of BSA dramatically decreased, which indicated that a Förster nonradiative energy transfer process occurred through the formation of chemical bonds between BSA and CdTe/HA composites. And the two-dimensional correlation (2D COS was used to analyze the BSA solution before and after the reaction, which indicated that CdTe/HA composites have bound to a site at the surface of the molecule in the first subdomain IA. We also found that there was a linear relationship between the fluorescence intensity enhancement (F/F0 of CdTe/HA composites and the concentration of the bovine serum albumin, which might become a method for quantitative analysis of BSA in a real sample.

Tracing sources of pollution in soils from the Jinding Pb–Zn mining district in China using cadmium and lead isotopes

International Nuclear Information System (INIS)

Wen, Hanjie; Zhang, Yuxu; Cloquet, Christophe; Zhu, Chuanwei; Fan, Haifeng; Luo, Chongguang

2015-01-01

Highlights: • Cd isotopes can provide information on the emission, sources, and deposition of Cd. • Binary mixing model is established to trace pollution sources. • Dust transport is major pathway to transfer pollution in Jinding mine. - Abstract: Systematic variations in the Cd and Pb isotope ratios in polluted topsoils surrounding the Jinding Pb–Zn mine in China were measured so that the sources of the metals could be traced. The average δ 114/110 Cd value and 206 Pb/ 207 Pb isotope ratio in background soils from the region were +0.41‰ and 1.1902, respectively, whereas the contaminated soil samples had different values, with the δ 114/110 Cd values varying between −0.59‰ and +0.33‰ and the 206 Pb/ 207 Pb isotope ratios varying between 1.1764 and 1.1896. We also measured the Cd and Pb isotopic compositions in oxide ores, sulfide ores, and slags, and found that binary mixing between ores and background soils could explain almost all of the variations in the Cd and Pb isotope ratios in the contaminated soils. This suggests that Cd and Pb pollution in the soils was mainly caused by the deposition of dust emitted during anthropogenic activities (mining and refining). The Pb and Cd isotope ratios clearly showed that contamination in soils in the northeastern part of the area was caused by surface mines and zinc smelters and their slagheaps, while contamination in soils in the southwestern part of the area also came from tailing ponds and underground mines. The main area of soil polluted by dust from Pb–Zn mining processes roughly extended for up to 5 km from the mine itself

Molten-droplet synthesis of composite CdSe hollow nanoparticles

KAUST Repository

Gullapalli, Sravani; Grider, Jason M.; Bagaria, Hitesh G.; Lee, Kyusung; Cho, Minjung; Colvin, Vicki L.; Jabbour, Ghassan E.; Wong, Michael

2012-01-01

Many colloidal synthesis routes are not scalable to high production rates, especially for nanoparticles of complex shape or composition, due to precursor expense and hazards, low yields, and the large number of processing steps. The present work describes a strategy to synthesize hollow nanoparticles (HNPs) out of metal chalcogenides, based on the slow heating of a low-melting-point metal salt, an elemental chalcogen, and an alkylammonium surfactant in octadecene solvent. The synthesis and characterization of CdSe HNPs with an outer diameter of 15.6 ± 3.5 nm and a shell thickness of 5.4 ± 0.9 nm are specifically detailed here. The HNP synthesis is proposed to proceed with the formation of alkylammonium-stabilized nano-sized droplets of molten cadmium salt, which then come into contact with dissolved selenium species to form a CdSe shell at the droplet surface. In a reaction-diffusion mechanism similar to the nanoscale Kirkendall effect it is speculated that the cadmium migrates outwardly through this shell to react with more selenium, causing the CdSe shell to thicken. The proposed CdSe HNP structure comprises a polycrystalline CdSe shell coated with a thin layer of amorphous selenium. Photovoltaic device characterization indicates that HNPs have improved electron transport characteristics compared to standard CdSe quantum dots, possibly due to this selenium layer. The HNPs are colloidally stable in organic solvents even though carboxylate, phosphine, and amine ligands are absent; stability is attributed to octadecene-selenide species bound to the particle surface. This scalable synthesis method presents opportunities to generate hollow nanoparticles with increased structural and compositional variety. © 2012 IOP Publishing Ltd.

Molten-droplet synthesis of composite CdSe hollow nanoparticles

KAUST Repository

Gullapalli, Sravani

2012-11-16

Many colloidal synthesis routes are not scalable to high production rates, especially for nanoparticles of complex shape or composition, due to precursor expense and hazards, low yields, and the large number of processing steps. The present work describes a strategy to synthesize hollow nanoparticles (HNPs) out of metal chalcogenides, based on the slow heating of a low-melting-point metal salt, an elemental chalcogen, and an alkylammonium surfactant in octadecene solvent. The synthesis and characterization of CdSe HNPs with an outer diameter of 15.6 ± 3.5 nm and a shell thickness of 5.4 ± 0.9 nm are specifically detailed here. The HNP synthesis is proposed to proceed with the formation of alkylammonium-stabilized nano-sized droplets of molten cadmium salt, which then come into contact with dissolved selenium species to form a CdSe shell at the droplet surface. In a reaction-diffusion mechanism similar to the nanoscale Kirkendall effect it is speculated that the cadmium migrates outwardly through this shell to react with more selenium, causing the CdSe shell to thicken. The proposed CdSe HNP structure comprises a polycrystalline CdSe shell coated with a thin layer of amorphous selenium. Photovoltaic device characterization indicates that HNPs have improved electron transport characteristics compared to standard CdSe quantum dots, possibly due to this selenium layer. The HNPs are colloidally stable in organic solvents even though carboxylate, phosphine, and amine ligands are absent; stability is attributed to octadecene-selenide species bound to the particle surface. This scalable synthesis method presents opportunities to generate hollow nanoparticles with increased structural and compositional variety. © 2012 IOP Publishing Ltd.

Stable hydrogen, oxygen and sulfur isotopes composition in different tissues of cattle

International Nuclear Information System (INIS)

Sun Fengmei; Shi Guangyu; Wang Huiwen; Yang Shuming

2012-01-01

In order to research on stable hydrogen, oxygen, sulfur isotopes composition in different tissues of cattle, as well as the breed, δ 2 H and δ 34 S values of different defatted muscle, cattle tail hair, blood, liver, also δ 2h and δ 18 O values of water from muscle were determined by isotope ratio mass spectrometry. The stable sulfur isotope composition was not affected by cattle variety, meanwhile the hydrogen was uncertain; the δ 2 H and δ 34 S values between different defatted muscle, blood, liver, cattle hair were significantly different, at the same time the δ 34 S and δ 2 H values between each tissue were not significantly correlated; the δ 2 H values were strongly correlated with the δ 18 O values of muscle water. The above results indicated that stable sulfur and hydrogen isotopes fractionation in the various tissues were discrepant, thus the proper tissue should be selected according to the purpose and object in the beef traceability. (authors)

Low-Cost Lattice Matching Si Based Composite Substrates for HgCdTe

Science.gov (United States)

2013-09-01

211). ..............................................5 Figure 3. Relationship between calculated alloy compositions based on Se/CdTe BEP ratio and...Se:CdTe beam equivalent pressure ( BEP ) ratios. During CdSeTe growth, Se and Te are in competition for the same nucleation sites. If we assume that all...therefore, x(cal) = ΦSe/ΦCd = 2ΦSe/ΦCdTe, where Φ is the BEP of the material, measured by the nude ion gauge at the substrate position. Figure 3 shows the

Development of helium isotopic database in Japan

International Nuclear Information System (INIS)

Kusano, Tomohiro; Asamori, Koichi; Umeda, Koji

2012-09-01

We constructed “Helium Isotopic Database in Japan”, which includes isotope ratios of noble gases and chemical compositions of gas samples collected from hot springs and drinking water wells. The helium isotopes are excellent natural tracers for indicating the presence of mantle derived volatiles, because they are chemically inert and thus conserved in crustal rock-water systems. It is common knowledge that mantle degassing does not occur homogeneously over the Earth's surface. The 3 He/ 4 He ratios higher than the typical crustal values are interpreted to indicate that transfer of mantle volatiles into the crust by processes or mechanisms such as magmatic intrusion, faulting. In particular the spatial variation of helium isotope ratios could provide a valuable information to identify volcanic regions and tectonically active areas. The database was compiled geochemical data of hot spring gas etc. from 108 published papers. As a result of the data compiling, the database has 1728 helium isotopic data. A CD-ROM is attached as an appendix. (author)

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)

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

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.

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.

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.

Novel GQD-PVP-CdS composite with enhanced visible-light-driven photocatalytic properties

International Nuclear Information System (INIS)

Fan, Tao; Li, Yinle; Shen, Jianfeng; Ye, Mingxin

2016-01-01

Graphical abstract: - Highlights: • GQD-PVP-CdS composite was prepared for the first time through a facile hydrothermal route. • GQD-PVP-CdS demonstrated outstanding photoactivity under visible light illumination. • GQDs and polymeric material are compounded with CdS nanoparticles simultaneously for the first time. • The addition of GQDs plays pivotal roles in the enhancement of the photoactivity. - Abstract: A facile one-step hydrothermal method to synthesize graphene quantum dots (GQDs)-polyvinyl pyrrolidone (PVP)-CdS nanocomposite was reported. The nanocomposite was thoroughly characterized with X-ray diffraction, transmission electron microscopy, scanning electron microscopy, Fourier-transform infrared spectroscopy, Raman spectroscopy, X-ray photoelectron spectroscopy and ultraviolet–visible spectroscopy. The results confirmed the formation of GQD-PVP-CdS composite with a uniform size (5–10 nm) and a relatively low band gap (E_g = 2.23 eV). Moreover, the as-prepared composite exhibited enhanced photocatalytic activity toward the degradation of organic contaminants, with 92.3% of methyl orange (10 mg/L) removed after 3 hours of visible light illumination. This enhancement in photocatalytic activity was postulated to be attributed to the upconversion property of GQDs and a more efficient charge distribution between GQDs and CdS particles.

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)

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

High-precision isotopic characterization of USGS reference materials by TIMS and MC-ICP-MS

Science.gov (United States)

Weis, Dominique; Kieffer, Bruno; Maerschalk, Claude; Barling, Jane; de Jong, Jeroen; Williams, Gwen A.; Hanano, Diane; Pretorius, Wilma; Mattielli, Nadine; Scoates, James S.; Goolaerts, Arnaud; Friedman, Richard M.; Mahoney, J. Brian

2006-08-01

The Pacific Centre for Isotopic and Geochemical Research (PCIGR) at the University of British Columbia has undertaken a systematic analysis of the isotopic (Sr, Nd, and Pb) compositions and concentrations of a broad compositional range of U.S. Geological Survey (USGS) reference materials, including basalt (BCR-1, 2; BHVO-1, 2), andesite (AGV-1, 2), rhyolite (RGM-1, 2), syenite (STM-1, 2), granodiorite (GSP-2), and granite (G-2, 3). USGS rock reference materials are geochemically well characterized, but there is neither a systematic methodology nor a database for radiogenic isotopic compositions, even for the widely used BCR-1. This investigation represents the first comprehensive, systematic analysis of the isotopic composition and concentration of USGS reference materials and provides an important database for the isotopic community. In addition, the range of equipment at the PCIGR, including a Nu Instruments Plasma MC-ICP-MS, a Thermo Finnigan Triton TIMS, and a Thermo Finnigan Element2 HR-ICP-MS, permits an assessment and comparison of the precision and accuracy of isotopic analyses determined by both the TIMS and MC-ICP-MS methods (e.g., Nd isotopic compositions). For each of the reference materials, 5 to 10 complete replicate analyses provide coherent isotopic results, all with external precision below 30 ppm (2 SD) for Sr and Nd isotopic compositions (27 and 24 ppm for TIMS and MC-ICP-MS, respectively). Our results also show that the first- and second-generation USGS reference materials have homogeneous Sr and Nd isotopic compositions. Nd isotopic compositions by MC-ICP-MS and TIMS agree to within 15 ppm for all reference materials. Interlaboratory MC-ICP-MS comparisons show excellent agreement for Pb isotopic compositions; however, the reproducibility is not as good as for Sr and Nd. A careful, sequential leaching experiment of three first- and second-generation reference materials (BCR, BHVO, AGV) indicates that the heterogeneity in Pb isotopic compositions

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)

Karst springs as 'natural' pluviometers: Constraints on the isotopic composition of rainfall in the Apennines of central Italy

Energy Technology Data Exchange (ETDEWEB)

Minissale, A., E-mail: minissa@igg.cnr.it [CNR - Italian Council for Research, Institute of Geosciences and Earth Resources (Section of Florence) - Via La Pira 4, 50121 Firenze (Italy); Vaselli, O. [CNR - Italian Council for Research, Institute of Geosciences and Earth Resources (Section of Florence) - Via La Pira 4, 50121 Firenze (Italy)] [Department of Earth Sciences, University of Florence - Via La Pira 4, 50121 Firenze (Italy)

2011-05-15

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 {delta}{sup 18}O and {delta}D data and the {delta}{sup 18}O (and/or {delta}D) 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 {delta}{sup 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

Tracking nitrous oxide emission processes at a suburban site with semicontinuous, in situ measurements of isotopic composition

Science.gov (United States)

Harris, Eliza; Henne, Stephan; Hüglin, Christoph; Zellweger, Christoph; Tuzson, Béla; Ibraim, Erkan; Emmenegger, Lukas; Mohn, Joachim

2017-02-01

The isotopic composition of atmospheric nitrous oxide (N2O) was measured semicontinuously, at ˜35 min frequency in intermittent periods of 1-6 days over one and a half years, using preconcentration coupled to a quantum cascade laser spectrometer at the suburban site of Dübendorf, Switzerland. The achieved measurement repeatability was 0.08‰, 0.11‰, and 0.10‰ for δ18O, site preference, and δ15Nbulk respectively, which is better than or equal to standard flask sampling-based isotope ratio mass spectrometry performance. The observed mean diurnal cycle reflected the buildup of N2O from isotopically light sources on an isotopically heavy tropospheric background. The measurements were used to determine the source isotopic composition, which varied significantly compared to chemical and meteorological parameters monitored at the site. FLEXPART-COSMO transport modeling in combination with modified Emissions Database for Global Atmospheric Research inventory emissions was used to model N2O mole fractions at the site. Additionally, isotopic signatures were estimated for different source categories using literature data and used to simulate N2O isotopic composition over the measurement period. The model was able to capture variability in N2O mole fraction well, but simulations of isotopic composition showed little agreement with observations. In particular, measured source isotopic composition exhibited one magnitude larger variability than simulated, clearly indicating that the range of isotopic source signatures estimated from literature significantly underestimates true variability of source signatures. Source δ18O signature was found to be the most sensitive tracer for urban/industry versus agricultural N2O. δ15Nbulk and site preference may provide more insight into microbial and chemical emission processes than partitioning of anthropogenic source categories.

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

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

Certification of the Cu and Cd amount contents in artificial food digest using isotope dilution inductively coupled plasma mass spectrometry for Pilot Study 13 of the Comite Consultatif pour la Quantite de Matiere

International Nuclear Information System (INIS)

Vassileva, E.; Quetel, C.R.; Petrov, I.

2003-01-01

The Comite Consultatif pour la Quantite de Matiere (CCQM) launched the Pilot Study 13, an interlaboratory comparison between the metrological organizations worldwide on the determination of Ca, Cu and Cd in artificial food digests. These samples (available in 7% HNO 3 and with a salinity evaluated around 370 mg kg -1 , including approx. 30 mg Na kg -1 ) were prepared by gravimetrical mixing, and thus reference values traceable to the Kg for the three elements were available eventually. This paper describes the contribution of IRMM for the certification of the Cu and the Cd amount contents. The analytical protocol developed was based on isotope dilution associated to inductively coupled plasma mass spectrometry (ID-ICP-MS). The Cu measurements required 125-fold dilution of the initial sample solution. An interference of 23 Na 40 Ar + on 63 Cu + was identified but, since the ratio between both species was over 1000, it was successfully overcome by the calculation of a correction factor for its effect on the Cu amount content directly. Dilution of the sample was not possible for Cd only present at the low ng g -1 level. Up to 1% difference was observed on Cd isotope ratio results between measurements performed directly or after matrix separation. This is rarely shown. As similar results could be obtained either way after the necessary corrections, the direct measurements approach associated to a correction for mass discrimination effects using the CCQM-P13 sample itself (and the IUPAC table values as reference for the natural Cd isotopic composition) was preferred as it was the easiest. SI traceable values were obtained for Cu and Cd with less than 1 and 1.5% combined uncertainty, respectively (6 995±55 (k=2) nmol kg -1 and 45.53±0.64 (k=2) nmol kg -1 ). The excellent agreement between these results and the reference values (less than 0.6 and 0.08% difference) further validated the analytical protocols developed

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)

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.

Synthesis and characterization of CdS nanocrystallites and OMWCNT-supported cadmium sulfide composite and their photocatalytic activity under visible light irradiation

International Nuclear Information System (INIS)

Pawar, Amol S.; Garje, Shivram S.; Revaprasadu, Neerish

2016-01-01

CdS nanocrystallites and CdS- oxidized multiwalled carbon nanotubes (OMWCNT) composite were prepared by the solvothermal decomposition of a single-source molecular precursor, [Cd(pip.dtc) 2 ] (pip.dtc = piperidine dithiocarbamate) in the presence of ethylene glycol. The as prepared CdS nanocrystallites and CdS-OMWCNT composite were characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), UV-vis and Raman spectroscopy. Peak broadening in the XRD shows the formation of nanocrystalline CdS. TEM images of CdS nanocrystallites revealed the nearly spherical shape morphology of the particles, whereas, TEM images of composite showed the deposition of CdS nanocrystallites on the OMWCNT. EDX measurements matches with a 1:1 stoichiometry of Cd and S in CdS nanocrystallites, whereas, that of the composite showed the presence of Cd and S along with C. The vibrational properties of CdS nanocrystallites and their composite with OMWCNT were studied by Raman spectroscopy. Furthermore, the photocatalytic activity studies for the degradation of methylene blue under visible light irradiation using these materials were carried out. The surface area calculated using BET surface analyzer for CdS-OMWCNT composite (148.31 m 2 /g) was found to be more compared to bare CdS nanocrystallites (56.78 m 2 /g). The CdS-OMWCNT composite exhibited very good photocatalytic activity for the degradation of methylene blue under visible light irradiation which has been attributed to the increased surface area and synergistic effect in the composite compared to bare CdS nanocrystallites. - Highlights: • The carbon based nanocomposite of CdS (CdS-OMWCNT) have been prepared. • Simple solvothermal decomposition method has been used. • Single-source molecular precursor in presence of carbon nanotubes has been employed. • The photocatalytic activity of CdS NPs and CdS-OMWCNT composite have been

Synthesis of CdS/ZnO/graphene composite with high-efficiency photoelectrochemical activities under solar radiation

Science.gov (United States)

Han, Weijia; Ren, Long; Qi, Xiang; Liu, Yundan; Wei, Xiaolin; Huang, Zongyu; Zhong, Jianxin

2014-04-01

A novel ternary CdS/ZnO/graphene composite has been successfully prepared by loading ZnO and CdS nanoparticles in graphene nanosheets via a facile one-step hydrothermal method. The microstructures and properties have been examined by X-ray diffraction (XRD), scanning electron microscopy with an energy dispersive spectroscope (EDS), transmission electron microscopy, Raman and UV-vis diffuse reflectance spectra (DRS). The characterization results reveal that the crystalline of the composite is very well, the graphene sheets were tightly coated with ZnO and CdS nanoparticles, and the light-harvesting was effectively strengthened. Taking photoelectrochemical test, the ternary CdS/ZnO/graphene composite exhibits enhanced photocatalytic activity compared with its foundation matrix binary composites and pure ZnO and CdS. The improved photocatalytic performance can be attributed to the enhanced light absorption, the extremely efficient charge separation, as well as superior durability of the ternary composite. It is proposed that graphene-based composites by coupling graphene to suitable, multiple semiconductors can not only greatly improve the capacity for photocatalytic, but also expand the exploration and utilization of graphene-based nanocomposites for energy conversion.

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.

Changes in Isotopic Composition of Bottled Natural Waters Due to Different Storage Conditions

Energy Technology Data Exchange (ETDEWEB)

Ferjan, T. [Geological Survey of Slovenia, Department of Hydrogeology, Ljubljana (Slovenia); Brencic, M. [Faculty of Natural Sciences and Engineering, Department of Geology, and Geological Survey of Slovenia, Department of Hydrogeology, Ljubljana (Slovenia); Vreca, P. [Jozef Stefan Institute, Department of Environmental Sciences, Ljubljana (Slovenia)

2013-07-15

To establish the influence of environmental conditions on processes affecting the stable isotopic composition of bottled water during storage, various brands of bottled water were exposed for 2 years in different conditions. Selected low mineralized natural mineral water of one particular brand stored in polyethylene terephthalate (PET) bottles was placed at three different locations with different physical conditions (temperature, relative humidity, air pressure, exposure to sunlight). For comparison, bottles of three other low mineralized natural mineral water brands, each from a different aquifer source, were placed in parallel at one of the locations. Each location was characterized by temperature, relative humidity and air pressure measurements. pH, conductivity and stable isotopic composition of oxygen, hydrogen and carbon in dissolved inorganic carbon ({delta}{sup 18}O, {delta}{sup 2}H, {delta}{sup 13}C{sub DIC}) were measured in regular intervals for nearly two years. Preliminary results from each location show noticeable changes in isotopic composition as well as the physical parameters of water with time of storage.

Environmental isotopes, chemical composition and groundwater sources in Al-Maghara area, Sinai, Egypt

International Nuclear Information System (INIS)

Nada, A.A.; Awad, M.A.; Froehlich, K.; El Behery, M.

1991-01-01

Groundwater samples collected from a number of localities, in Al-Maghara area, north central part of Sinai, were subject to various chemical and isotopic analysis. The purpose of the study is to determine whether the groundwaters are recently recharged or not in order to adopt an efficient water management policy. The hydrochemical results indicate that they are mainly of primary marine origin, dilution of this water by meteoric water changes its chemical composition to be mixed water type, which has the major chemical components: KCl, NaCl, Na 2 SO 4 , MgSO 4 , Mg(HCO 3 ) 2 and Ca(HCO 3 ) 2 . The tritium content confirm the meteoric water recharge recently especially for wells with high tritium content. The stable environmental isotopic composition of the groundwater reflects the isotopic composition of precipitation and flooding with some evaporation enrichment prior to infiltration. There is also mixing with palaeowater (water recharge in the past cooler climate periods), by leaking through faulting in the area. (orig.) [de

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

The features of the isotope composition of carbon in the Paleozoic and Mesozoic oils of Western Siberia

Energy Technology Data Exchange (ETDEWEB)

Golyshev, S.I.; Lebedena, L.V.

1984-01-01

The isotope composition of the carbon in the oils from the Mesozoic and Paleozoic deposits is measured. The variations in the isotope composition of carbon for the Paleozoic oils is between 27.5 and 30.8 percent, while for the oils from the lower Jurassic and Triassic levels it is between 27.7 and 31.2 percent and for the upper Jurassic oils it is between 30.1 and 34.5 percent. The dependence of the isotope composition of the carbon in the oils on the type of original organic matter and its metamorphosis conditions during lithogenesis is analyzed. A softening in the isotope composition of the carbon in the oils from the oceanic deposits relative to continental deposits is found, together with a genetic individualism of the oils from the Paleozoic deposits and their difference from the oils in the Mesozoic deposits.

Polyaniline/carbon nanotube/CdS quantum dot composites with enhanced optical and electrical properties

Science.gov (United States)

Goswami, Mrinmoy; Ghosh, Ranajit; Maruyama, Takahiro; Meikap, Ajit Kumar

2016-02-01

A new kind of polyaniline/carbon nanotube/CdS quantum dot composites have been developed via in-situ polymerization of aniline monomer in the presence of dispersed CdS quantum dots (size: 2.7-4.8 nm) and multi-walled carbon nanotubes (CNT), which exhibits enhanced optical and electrical properties. The existences of 1st order, 2nd order, and 3rd order longitudinal optical phonon modes, strongly indicate the high quality of synthesized CdS quantum dots. The occurrence of red shift of free exciton energy in photoluminescence is due to size dependent quantum confinement effect of CdS. The conductivity of the composites (for example PANI/CNT/CdS (2 wt.% CdS)) is increased by about 7 of magnitude compared to that of pure PANI indicating a charge transfer between CNT and polymer via CdS quantum dots. This advanced material has a great potential for high-performance of electro-optical applications.

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

Physical and Human Controls on the Carbon Composition of Organic Matter in Tropical Rivers: An Integrated Analysis of Landscape Properties and River Isotopic Composition

Energy Technology Data Exchange (ETDEWEB)

Ballester, M. V.R.; Victoria, R. L.; Krusche, A. V. [Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Piracicaba (Brazil); Bernardes, M. [Universidade Federal Fluminense, Rio de Janeiro (Brazil); Neill, C.; Deegan, L. [Marine Biological Laboratory, Woods Hole, MA (United States); Richey, J. E. [University of Washington, Seatle, WA (United States)

2013-05-15

We applied an integrated analysis of landscape properties including soil properties, land cover and riverine isotopic composition. To evaluate physical and human controls on the carbon composition of organic matter in tropical rivers, we applied an integrated analysis of landscape properties including soil properties, land cover and riverine isotopic composition. Our main objective was to establish the relationship between basin attributes and forms, fluxes and composition of dissolved and particulate organic matter in river channels. A physical template was developed as a GIS-based comprehensive tool to support the understanding of the biogeochemistry of the surface waters of two tropical rivers: the Ji-Parana (Western Amazonia) and the Piracicaba (southeastern of Brazil). For each river we divided the basin into drainage units, organized according to river network morphology and degree of land use impact. Each sector corresponded to a sampling point where river isotopic composition was analysed. River sites and basin characteristics were calculated using datasets compiled as layers in ArcGis Geographical Information System and ERDAS-IMAGINE (Image Processing) software. Each delineated drainage area was individually characterized in terms of topography, soils, river network and land use. Carbon stable isotopic composition of dissolved organic matter (DOM) and particulate organic matter (POM) was determined at several sites along the main tributaries and small streams. The effects of land use on fluvial carbon composition were quantified by a linear regression analysis, relating basin cover and river isotopic composition. The results showed that relatively recent land cover changes have already had an impact on the composition of the riverine DOM and POM, indicating that, as in natural ecosystems, vegetation plays a key role in the composition of riverine organic matter in agricultural ecosystems. (author)

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

Determination of Cd and Pb in human blood by isotope dilution inductively coupled plasma mass spectrometry : International comparison

International Nuclear Information System (INIS)

Park, Chang Joon; Suh, Jeong Ki; Lee, Sang Hwa

1996-01-01

Inorganic analytical laboratory of Korea Research Institute of Standards and Science participated in an interlaboratory comparison program operated by Quebec Toxicology Centre of Canada in 1994 and again in 1995. The objective of this program is to enable participating laboratories to assess reproducibility and accuracy of their analytical results for trace toxic elements in human biological fluids. This laboratory determined Cd and Pb concentrations in 3 levels of human blood samples by isotope dilution inductively coupled plasma mass spectrometry. 0.5 mL of blood sample is added to the digestion bomb together with 2 mL of nitric acid and enriched spike isotopes and then decomposed in the microwave digestion system. The decomposed sample is diluted to 10 mL and nebulized into ICP-MS. The Cd and Pb values reported by all participating laboratories are presented and compared. The values reported by this laboratory are within the acceptable range of target values. (author)

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)

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.

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)

Grain size effect on Sr and Nd isotopic compositions in eolian dust. Implications for tracing dust provenance and Nd model age

International Nuclear Information System (INIS)

Feng Jinliang; Zhu Liping; Zhen Xiaolin; Hu Zhaoguo

2009-01-01

Strontium (Sr) and neodymium (Nd) isotopic compositions enable identification of dust sources and reconstruction of atmospheric dispersal pathways. The Sr and Nd isotopic compositions in eolian dust change systematically with grain size in ways not yet fully understood. This study demonstrates the grain size effect on the Sr and Nd isotopic compositions in loess and 2006 dust fall, based on analyses of seven separated grain size fractions. The analytical results indicate that Sr isotopic ratios strongly depend on the grain size fractions in samples from all types of eolian dust. In contrast, the Nd isotopic ratios exhibit little variation in loess, although they vary significantly with grain size in samples from a 2006 dust fall. Furthermore, Nd model ages tend to increase with increasing grain size in samples from all types of eolian dust. Comparatively, Sr isotopic compositions exhibit high sensitively to wind sorting, while Nd isotopic compositions show greater sensitively to dust origin. The principal cause for the different patterns of Sr and Nd isotopic composition variability with grain size appears related to the different geochemical behaviors between rubidium (Rb) and Sr, and the similar geochemical behaviors between samarium (Sm) and Nd. The Nd isotope data indicate that the various grain size fractions in loess have similar origins for each sample. In contrast, various provenance components may separate into different grain size fractions for the studied 2006 dust fall. The Sr and Nd isotope compositions further confirm that the 2006 dust fall and Pleistocene loess in Beijing have different sources. The loess deposits found in Beijing and those found on the Chinese Loess Plateau also derive from different sources. Variations between Sr and Nd isotopic compositions and Nd model ages with grain size need to be considered when directly comparing analyses of eolian dust of different grain size. (author)

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 ...

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)

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)

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

Tungsten isotopic compositions of iron meteorites: Chronological constraints vs. cosmogenic effects

Science.gov (United States)

Markowski, A.; Quitté, G.; Halliday, A. N.; Kleine, T.

2006-02-01

High-precision W isotopic compositions are presented for 35 iron meteorites from 7 magmatic groups (IC, IIAB, IID, IIIAB, IIIF, IVA, and IVB) and 3 non-magmatic groups (IAB, IIICD, and IIE). Small but resolvable isotopic variations are present both within and between iron meteorite groups. Variations in the 182W/ 184W ratio reflect either time intervals of metal-silicate differentiation, or result from the burnout of W isotopes caused by a prolonged exposure to galactic cosmic rays. Calculated apparent time spans for some groups of magmatic iron meteorites correspond to 8.5 ± 2.1 My (IID), 5.1 ± 2.3 My (IIAB), and 5.3 ± 1.3 My (IVB). These time intervals are significantly longer than those predicated from models of planetesimal accretion. It is shown that cosmogenic effects can account for a large part of the W isotopic variation. No simple relationship exists with exposure ages, compromising any reliable method of correction. After allowance for maximum possible cosmogenic effects, it is found that there is no evidence that any of the magmatic iron meteorites studied here have initial W isotopic compositions that differ from those of Allende CAIs [ ɛ182W = - 3.47 ± 0.20; [T. Kleine, K. Mezger, H. Palme, E. Scherer and C. Münker, Early core formation in asteroids and late accretion of chondrite parent bodies: evidence from 182Hf- 182W in CAIs, metal-rich chondrites and iron meteorites, Geochim. Cosmochim. Acta (in press)]. Cosmogenic corrections cannot yet be made with sufficient accuracy to obtain highly precise ages for iron meteorites. Some of the corrected ages nevertheless require extremely early metal-silicate segregation no later than 1 My after formation of CAIs. Therefore, magmatic iron meteorites appear to provide the best examples yet identified of material derived from the first planetesimals that grew by runaway growth, as modelled in dynamic simulations. Non-magmatic iron meteorites have a more radiogenic W isotopic composition than magmatic

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.

Tracing anthropogenic thallium in soil using stable isotope compositions.

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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.

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

Synthesis and crystalline properties of CdS incorporated polyvinylidene fluoride (PVDF) composite film

Science.gov (United States)

Patel, Arunendra Kumar; Sunder, Aishwarya; Mishra, Shweta; Bajpai, Rakesh

2018-05-01

This paper gives an insight on the synthesis and crystalline properties of Polyvinylidene Fluoride (PVDF) (host matrix) composites impregnated with Cadmium Sulphide (CdS) using Dimethyl formamide (DMF) as the base, prepared by the well known solvent casting technique. The effect of doping concentration of CdS in to the PVDF matrix was studied using X-ray diffraction technique. The structural properties like crystallinity Cr, interplanar distance d, average size of the crystalline region (D), and average inter crystalline separation (R) have been estimated for the developed composite. The crystallinity index, crystallite size and inter crystalline separation is increasing with increase in the concentration of CdS in to the PVDF matrix while the interplanar distance d is decreasing.

Incorporation of N–ZnO/CdS/Graphene oxide composite photocatalyst for enhanced photocatalytic activity under visible light

Energy Technology Data Exchange (ETDEWEB)

Huo, Pengwei, E-mail: huopw1@163.com [School of Chemistry & Chemical Engineering Jiangsu University Zhenjiang, 212013 (China); Institute of Green Chemistry and Chemical Technology, Jiangsu University, Zhenjiang, 212013 (China); Zhou, Mingjun; Tang, Yanfeng [School of Chemistry & Chemical Engineering Jiangsu University Zhenjiang, 212013 (China); Liu, Xinlin [School of Energy & Power Engineering Jiangsu University Zhenjiang, 212013 (China); Ma, Changchang; Yu, Longbao [School of Chemistry & Chemical Engineering Jiangsu University Zhenjiang, 212013 (China); Yan, Yongsheng, E-mail: yys@mail.ujs.edu.cn [School of Chemistry & Chemical Engineering Jiangsu University Zhenjiang, 212013 (China); Institute of Green Chemistry and Chemical Technology, Jiangsu University, Zhenjiang, 212013 (China)

2016-06-15

N–ZnO/CdS/Graphene oxide (GO) composite photocatalysts have been successfully synthesized by hydrothermal method. The as-prepared composite photocatalysts were characterized by X-ray diffraction (XRD), Raman, scanning electron microscopy(SEM), transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), fourier transform infrared (FT-IR) spectra, UV–vis diffuse reflectance spectra (UV–vis DRS), thermogravimetry (TG) and photoluminescence (PL). The as-prepared photocatalysts exhibited strong visible light photocatalytic activity toward to degradation of antibiotics under ambient conditions. Particularly, the N–ZnO/CdS/GO composite photocatalysts showed the higher photocatalytic degradation rate (86%) of ciprofloxacin CIP under visible light irradiation than the pure photocatalysts. Compared with degradation of different antibiotics (tetracycline (TC), oxytetracycline hydrochloride (OTC-HCl) and levofloxacin (LEV)), the N–ZnO/CdS/GO composite photocatalysts also exhibited high photocatalytic activities. According to the experiments, the role of GO in the composite photocatalysts acted as an electron conductor, and also enhanced the separation rate of electrons and holes which greatly improved the photocatalytic activity. Lastly, the mechanism of enhanced photocatalytic degradation of CIP was also discussed. - Highlights: • N–ZnO/CdS/GO composite was synthesized by the hydrothermal processes. • N–ZnO/CdS composites prevent pure CdS or ZnO from photocorrosion. • N–ZnO/CdS/GO shows the remarkable photocatalytic activity and stability.

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)

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)

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

Interpretation of groundwater origin in the Velenje coal mine on the basis of isotope composition

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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.

Plutonium isotopic composition of high burnup spent fuel discharged from light water reactors

International Nuclear Information System (INIS)

Nakano, Yoshihiro; Okubo, Tsutomu

2011-01-01

Highlights: → Pu isotopic composition of fuel affects FBR core nuclear characteristics very much. → Spent fuel compositions of next generation LWRs with burnup of 70 GWd/t were obtained. → Pu isotopic composition and amount in the spent fuel with 70 GWd/t were evaluated. → Spectral shift rods of high burnup BWR increases the fissile Pu fraction of spent fuel. → Wide fuel rod pitch of high burnup PWR lowers the fissile Pu fraction of spent fuel. - Abstract: The isotopic composition and amount of plutonium (Pu) in spent fuel from a high burnup boiling water reactor (HB-BWR) and a high burnup pressurized water reactor (HB-PWR), each with an average discharge burnup of 70 GWd/t, were estimated, in order to evaluate fast breeder reactor (FBR) fuel composition in the transition period from LWRs to FBRs. The HB-BWR employs spectral shift rods and the neutron spectrum is shifted through the operation cycle. The weight fraction of fissile plutonium (Puf) isotopes to the total plutonium in HB-BWR spent fuel after 5 years cooling is 62%, which is larger than that of conventional BWRs with average burnup of 45 GWd/t, because of the spectral shift operation. The amount of Pu produced in the HB-BWR is also larger than that produced in a conventional BWR. The HB-PWR uses a wider pitch 17 x 17 fuel rod assembly to optimize neutron slowing down. The Puf fraction of HB-PWR spent fuel after 5 years cooling is 56%, which is smaller than that of conventional PWRs with average burnup of 49 GWd/t, mainly because of the wider pitch. The amount of Pu produced in the HB-PWR is also smaller than that in conventional PWRs.

Chemical analyses and calculation of isotopic compositions of high-burnup UO{sub 2} fuels and MOX fuels

Energy Technology Data Exchange (ETDEWEB)

Matsumura, Tetsuo; Sasahara, Akihiro [Central Research Inst. of Electric Power Industry, Tokyo (Japan)

2001-08-01

Chemical analysis activities of isotopic compositions of high-burnup UO{sub 2} fuels and MOX fuels in CRIEPI and calculation evaluation are reviewed briefly. C/E values of ORIGEN2, in which original libraries and JENDL-3.2 libraries are used, and other codes with chemical analysis data are reviewed and evaluated. Isotopic compositions of main U and Pu in fuels can be evaluated within 10% relative errors by suitable libraries and codes. Void ratio is effective parameter for C/E values in BWR fuels. JENDL-3.2 library shows remarkable improvement compared with original libraries in isotopic composition evaluations of FP nuclides. (author)

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.

Estimation of the annual production and composition of C&D Debris in Galicia (Spain).

Science.gov (United States)

Martínez Lage, Isabel; Martínez Abella, Fernando; Herrero, Cristina Vázquez; Ordóñez, Juan Luis Pérez

2010-04-01

One of the key aspects that must be taken into consideration within the framework of Sustainable Construction is the management of Construction and Demolition (C&D) Debris. As for other types of waste, specific handling procedures are required to manage C&D Debris; these include reduction, reuse, recycling, and if all other possibilities fail, recovery or disposal. For public planning strategies aimed at the management of C&D Debris to be effective, it is first necessary to have specific knowledge of the type of waste materials generated in a particular region. After verifying that the methods available to determine the production and composition of C&D Debris are limited, this paper presents a procedure to ascertain the production and composition of C&D Debris, in any region. The procedure utilizes data on the surface areas of newly constructed buildings, renovations and demolitions, which are estimated from available data for recent years, as well as information on the quantity of debris generated per surface area in any type of construction site, which is obtained from recently executed constructions or from the ground plans of older buildings. The method proposed here has been applied to Galicia, one of Spain's autonomous communities, for which the quantity and composition of C&D Debris have been estimated for the horizon year 2011. Copyright 2009 Elsevier Ltd. All rights reserved.

Coexistence of galenas with different Pb isotopic composition in Los Pedroches batholith area (Spain)

Science.gov (United States)

García de Madinabeitia, S.; Santos Zalduegui, J. F.; Larrea, F. J.; Carracedo, M.; Gil Ibarguchi, J. I.

2003-04-01

The Los Pedroches batholith region (S Spain) includes three separated mining districts: Linares, La Carolina and Los Pedroches. The Pb isotopic composition of thirty-three galenas from this sector has been measured. On the basis of the Pb data two types of mineralization are established. A first type including: (i) the Linares and La Carolina districts where ore-bearing filons cut Hercynian granites or their hostrocks (SE of the batholith), and (ii) the so-called "peribatholithic" ore bodies represented by scarce mines in the host-rock of the batholith; all of them exhibit homogeneous Pb isotopic compositions of: 206Pb/204Pb = 18.236, 207Pb/204Pb = 15.615, 208Pb/204Pb = 38.347 and a model age of ca. 324 Ma. The second type is represented by a huge N120^oE hydrotermal vein (the El Zumajo vein) intrusive in granitoid bodies of the batholith; the Pb isotopic composition of the vein is: 206Pb/204Pb = 18.457, 207Pb/204Pb = 15.636, 208Pb/204Pb = 38.611 and a model age of ca. 201 Ma. Analysed K-feldspars from batholithic granodiorite and granites have Pb isotopic compositions similar to those reported previously from Hercynian granites of the area (1) and to the galenas of Linares, La Carolina and "peribatholithic" ores. The whole dataset reveals a Pb evolution curve with μ_2 = 9.8 and ω_2 = 38.3, close to the model curve for the "orogen" (2). This suggests for Linares, La Carolina and the "peribatholithic" mineralizations a Pb source related to that of the granites. The pre-Tremadoc metasedimentary rocks of the area, with Pb isotopic composition (3) very close to that of feldspars and galenas studied is proposed as a possible source of Pb for both the granites and associated mineralizations, although the Pb isotopic composition of El Zumajo calls for a different origin. The observed difference in Pb isotopic ratios of the studied galenas points to, at least, two ore-forming events: (i) one relating older mineralizations and granitoid intrusives, in agreement with

Molecular Control of the Nanoscale: Effect of Phosphine–Chalcogenide Reactivity on CdS–CdSe Nanocrystal Composition and Morphology

Energy Technology Data Exchange (ETDEWEB)

Ruberu, T. Purnima A.; Albright, Haley R.; Callis, Brandon; Ward, Brittney; Cisneros, Joana; Fan, Hua-Jun; Vela, Javier

2012-04-22

We demonstrate molecular control of nanoscale composition, alloying, and morphology (aspect ratio) in CdS–CdSe nanocrystal dots and rods by modulating the chemical reactivity of phosphine–chalcogenide precursors. Specific molecular precursors studied were sulfides and selenides of triphenylphosphite (TPP), diphenylpropylphosphine (DPP), tributylphosphine (TBP), trioctylphosphine (TOP), and hexaethylphosphorustriamide (HPT). Computational (DFT), NMR (31P and 77Se), and high-temperature crossover studies unambiguously confirm a chemical bonding interaction between phosphorus and chalcogen atoms in all precursors. Phosphine–chalcogenide precursor reactivity increases in the order: TPPE < DPPE < TBPE < TOPE < HPTE (E = S, Se). For a given phosphine, the selenide is always more reactive than the sulfide. CdS1–xSex quantum dots were synthesized via single injection of a R3PS–R3PSe mixture to cadmium oleate at 250 °C. X-ray diffraction (XRD), transmission electron microscopy (TEM), and UV/Vis and PL optical spectroscopy reveal that relative R3PS and R3PSe reactivity dictates CdS1–xSex dot chalcogen content and the extent of radial alloying (alloys vs core/shells). CdS, CdSe, and CdS1–xSex quantum rods were synthesized by injection of a single R3PE (E = S or Se) precursor or a R3PS–R3PSe mixture to cadmium–phosphonate at 320 or 250 °C. XRD and TEM reveal that the length-to-diameter aspect ratio of CdS and CdSe nanorods is inversely proportional to R3PE precursor reactivity. Purposely matching or mismatching R3PS–R3PSe precursor reactivity leads to CdS1–xSex nanorods without or with axial composition gradients, respectively. We expect these observations will lead to scalable and highly predictable “bottom-up” programmed syntheses of finely heterostructured nanomaterials with well-defined architectures and properties that are tailored for precise applications.

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

Effect of Na, Ca and pH on simultaneous uptake of Cd, Cu, Ni, Pb, and Zn in the water flea Daphnia magna measured using stable isotopes

International Nuclear Information System (INIS)

Komjarova, I.; Blust, R.

2009-01-01

The present study investigates the effects of Na + , Ca 2+ and pH on the kinetics of Cd, Cu, Ni, Pb, and Zn uptake in Daphnia magna at low exposure concentrations measured using a stable isotope technique. Using experimental data the uptake rate constants were calculated for each metal individually on the basis of total metal concentrations. The copper uptake was not significantly affected by variations in chemical composition of the test medium. Calcium had a suppressing effect on the uptake of Cd, Ni, Pb and Zn. Specifically, Cd and Ni uptake rate constants decreased with increases in calcium concentrations from 0.1 to 2.5 mM. The uptake of Zn and Pb was significantly suppressed only at 2.5 mM Ca. The effect of sodium was less clear. There was no effect of varying sodium concentrations on the Ni uptake rate constants. Cd and Pb showed an increase in uptake rate constants at elevated sodium concentrations (2-8 mM Na + for Cd and 8 mM Na + for Pb). A bell-shaped response on increasing Na + concentrations was observed for Zn with a maximum value of uptake rate constant at the middle value (2 mM Na + ). Variation in pH of the medium affected Cd, Ni and Zn uptake processes. When Daphnia were exposed to acidic conditions (pH 6), the Cd and Ni uptake rate constants were the highest, while similarly low values were observed at neutral and basic conditions. In contrast, the uptake rates of Zn were linearly increasing with increasing pH of the medium.

CdS nanoparticles/CeO_2 nanorods composite with high-efficiency visible-light-driven photocatalytic activity

International Nuclear Information System (INIS)

You, Daotong; Pan, Bao; Jiang, Fan; Zhou, Yangen; Su, Wenyue

2016-01-01

Graphical abstract: Coupling CdS with CeO_2 can effectively improve the light-harvesting ability of wide-band gap CeO_2 NRs as the photoinduced electrons on the conduction band of CdS are transfered to the conduction band of CeO_2. - Highlights: • Coupling CdS can effectively improve the light-harvesting ability of wide-band gap CeO_2. • CdS/CeO_2 composites show high photocatalytic activity under visible light irradiation. • The mechanism of photocatalytic H_2 evolution over CdS/CeO_2 was proposed. - Abstract: Different mole ratios of CdS nanoparticles (NPs)/CeO_2 nanorods (NRs) composites with effective contacts were synthesized through a two-step hydrothermal method. The crystal phase, microstructure, optical absorption properties, electrochemical properties and photocatalytic H_2 production activity of these composites were investigated. It was concluded that the photogenerated charge carriers in the CdS NPs/CeO_2 NRs composite with a proper mole ratio (1:1) exhibited the longest lifetime and highest separation efficiency, which was responsible for the highest H_2-production rate of 8.4 mmol h"−"1 g"−"1 under visible-light irradiation (λ > 420 nm). The superior photocatalytic H_2 evolution properties are attributed to the transfer of visible-excited electrons of CdS NPs to CeO_2 NRs, which can effectively extend the light absorption range of wide-band gap CeO_2 NRs. This work provides feasible routes to develop visible-light responsive CeO_2-based nanomaterial for efficient solar utilization.

Quantifying the isotopic composition of NOx emission sources: An analysis of collection methods

Science.gov (United States)

Fibiger, D.; Hastings, M.

2012-04-01

We analyze various collection methods for nitrogen oxides, NOx (NO2 and NO), used to evaluate the nitrogen isotopic composition (δ15N). Atmospheric NOx is a major contributor to acid rain deposition upon its conversion to nitric acid; it also plays a significant role in determining air quality through the production of tropospheric ozone. NOx is released by both anthropogenic (fossil fuel combustion, biomass burning, aircraft emissions) and natural (lightning, biogenic production in soils) sources. Global concentrations of NOx are rising because of increased anthropogenic emissions, while natural source emissions also contribute significantly to the global NOx burden. The contributions of both natural and anthropogenic sources and their considerable variability in space and time make it difficult to attribute local NOx concentrations (and, thus, nitric acid) to a particular source. Several recent studies suggest that variability in the isotopic composition of nitric acid deposition is related to variability in the isotopic signatures of NOx emission sources. Nevertheless, the isotopic composition of most NOx sources has not been thoroughly constrained. Ultimately, the direct capture and quantification of the nitrogen isotopic signatures of NOx sources will allow for the tracing of NOx emissions sources and their impact on environmental quality. Moreover, this will provide a new means by which to verify emissions estimates and atmospheric models. We present laboratory results of methods used for capturing NOx from air into solution. A variety of methods have been used in field studies, but no independent laboratory verification of the efficiencies of these methods has been performed. When analyzing isotopic composition, it is important that NOx be collected quantitatively or the possibility of fractionation must be constrained. We have found that collection efficiency can vary widely under different conditions in the laboratory and fractionation does not vary

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

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.

Identification of contamination in a lake sediment core using Hg and Pb isotopic compositions, Lake Ballinger, Washington, USA

International Nuclear Information System (INIS)

Gray, John E.; Pribil, Michael J.; Van Metre, Peter C.; Borrok, David M.; Thapalia, Anita

2013-01-01

Highlights: ► Hg and Pb concentration and isotopic compositions traced anthropogenic sources. ► Concentrations and metal loadings of Hg and Pb increased during the smelting period. ► Hg isotopic compositions changed during smelting compared to the pre-smelting period. ► Data indicate mass independent fractionation of Hg isotopes. - Abstract: Concentrations and isotopic compositions of Hg and Pb were measured in a sediment core collected from Lake Ballinger, near Seattle, Washington, USA. Lake Ballinger has been affected by input of metal contaminants emitted from the Tacoma smelter, which operated from 1887 to 1986 and was located about 53 km south of the lake. Concentrations and loadings of Hg and Pb in Lake Ballinger increased by as much as three orders of magnitude during the period of smelting as compared to the pre-smelting period. Concentrations and loadings of Hg and Pb then decreased by about 55% and 75%, respectively, after smelting ended. Isotopic compositions of Hg changed considerably during the period of smelting (δ 202 Hg = −2.29‰ to −0.38‰, mean −1.23‰, n = 9) compared to the pre-smelting period (δ 202 Hg = −2.91‰ to −2.50‰, mean −2.75‰, n = 4). Variations were also observed in 206 Pb/ 207 Pb and 208 Pb/ 207 Pb isotopic compositions during these periods. Data for Δ 199 Hg and Δ 201 Hg indicate mass independent fractionation (MIF) of Hg isotopes in Lake Ballinger sediment during the smelting and post-smelting period and suggest MIF in the ore smelted, during the smelting process, or chemical modification at some point in the past. Negative values for Δ 199 Hg and Δ 201 Hg for the pre-smelting period are similar to those previously reported for soil, peat, and lichen, likely suggesting some component of atmospheric Hg. Variations in the concentrations and isotopic compositions of Hg and Pb were useful in tracing contaminant sources and the understanding of the depositional history of sedimentation in Lake Ballinger

Thallium isotope composition of the upper continental crust and rivers - An investigation of the continental sources of dissolved marine thallium

Science.gov (United States)

Nielsen, S.G.; Rehkamper, M.; Porcelli, D.; Andersson, P.; Halliday, A.N.; Swarzenski, P.W.; Latkoczy, C.; Gunther, D.

2005-01-01

The thallium (Tl) concentrations and isotope compositions of various river and estuarine waters, suspended riverine particulates and loess have been determined. These data are used to evaluate whether weathering reactions are associated with significant Tl isotope fractionation and to estimate the average Tl isotope composition of the upper continental crust as well as the mean Tl concentration and isotope composition of river water. Such parameters provide key constraints on the dissolved Tl fluxes to the oceans from rivers and mineral aerosols. The Tl isotope data for loess and suspended riverine detritus are relatively uniform with a mean of ??205Tl = -2.0 ?? 0.3 (??205Tl represents the deviation of the 205Tl/203Tl isotope ratio of a sample from NIST SRM 997 Tl in parts per 104). For waters from four major and eight smaller rivers, the majority were found to have Tl concentrations between 1 and 7 ng/kg. Most have Tl isotope compositions very similar (within ??1.5 ??205Tl) to that deduced for the upper continental crust, which indicates that no significant Tl isotope fractionation occurs during weathering. Based on these results, it is estimated that rivers have a mean natural Tl concentration and isotope composition of 6 ?? 4 ng/kg and ??205Tl = -2.5 ?? 1.0, respectively. In the Amazon estuary, both additions and losses of Tl were observed, and these correlate with variations in Fe and Mn contents. The changes in Tl concentrations have much lower amplitudes, however, and are not associated with significant Tl isotope effects. In the Kalix estuary, the Tl concentrations and isotope compositions can be explained by two-component mixing between river water and a high-salinity end member that is enriched in Tl relative to seawater. These results indicate that Tl can display variable behavior in estuarine systems but large additions and losses of Tl were not observed in the present study. Copyright ?? 2005 Elsevier Ltd.

Study of the matrix specific mass discrimination effects during inductively coupled plasma mass spectrometry isotope ratio measurements

International Nuclear Information System (INIS)

Vassileva, E.; Quetel, Ch.R.

2004-01-01

Sample matrix related effects on mass discrimination during inductively coupled plasma mass spectrometry (ICP-MS) isotope ratio measurements have only been rarely reported. However, they can lead to errors larger than the uncertainty claimed on the ratio results when not properly taken into account or corrected for. These matrix specific affects were experienced during an Isotope Dilution Mass Spectrometry (IDMS) campaign we carried out for the certification of the Cd amount content in some food digest samples (7% acidity and salts content around 450μg g -1 ). Dilution was not possible for Cd only present at the low ng g -1 level. Up to 1% difference was observed on Cd isotope ratio results between measurements performed directly or after matrix separation. This was a significant difference considering that less than 1.5% relative combined uncertainty was eventually estimated for these IDMS measurements. Similar results could be obtained either way after the implementation of necessary corrections. The direct measurement approach associated to a correction for mass discrimination effects using the food digest sample itself (and the IUPAC table values as reference for the natural Cd isotopic composition) was preferred as it was the easiest. Consequently, the impact of matrix effects on mass discrimination during isotope ratio measurements with two types of ICP- MS (quadrupole and magnetic sector instruments) was studied for 4 elements (Li, Cu, Cd and Tl). Samples of varying salinity (up to 0.25%) and acidity (up to 7%) characteristics were prepared using isotopic certified reference materials of these elements. The long term and short-term stability, respectively reproducibility and repeatability, of the results, as well as the evolution of the difference to certified ratio values were monitored. As expected the 13 investigated isotopic ratios were all sensitive to variations in salt and acid concentrations. Our experiments also showed that simultaneous variation

Extermination Of Uranium Isotopes Composition Using A Micro Computer With An IEEE-488 Interface For Mass Spectrometer Analysis

International Nuclear Information System (INIS)

Prajitno; Taftazani, Agus; Yusuf

1996-01-01

A mass spectrometry method can be used to make qualitative or quantitative analysis. For qualitative analysis, identification of unknown materials by a Mass Spectrometer requires definite assignment of mass number to peak on chart. In quantitative analysis, a mass spectrometer is used to determine isotope composition material in the sample. Analysis system of a Mass Spectrometer possession of PPNY-BATAN based on comparison ion current intensity which enter the collector, and have been used to analyse isotope composition. Calculation of isotope composition have been manually done. To increase the performance and to avoid manual data processing, a micro computer and IEEE-488 interface have been installed, also software packaged has been made. So that the determination of the isotope composition of material in the sample will be faster and more efficient. Tile accuracy of analysis using this program on sample standard U 3 O 8 NBS 010 is between 93,87% - 99,98%

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...

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

The precision of Tl isotopic measurements by thermal ionization mass spectrometry (TIMS) is severely limited by the fact that Tl possesses only two naturally occurring isotopes, such that there is no invariant isotope ratio that can be used to correct for instrumental mass discrimination. In this paper we describe new chemical and mass spectrometric techniques for the determination of Tl isotopic compositions at a level of precision hitherto unattained. Thallium is first separated from the geological matrix using a two-stage anion-exchange procedure. Thallium isotopic compositions are then determined by multiple-collector inductively coupled plasma-mass spectrometry with correction for mass discrimination using the known isotopic composition of Pb that is admixed to the sample solutions. With these procedures we achieve a precision of 0.01-0.02% for Tl isotope ratio measurements in geological samples and this is a factor of ≥3-4 better than the best published results by TIMS. However, without adequate precautions, experimental artifacts can be generated that result in apparent Tl isotopic fractionations of up to one per mil. Analysis of five terrestrial samples indicate the existence of Tl isotopic variations related to natural fractionation processes on the Earth. Two of the three igneous rocks analyzed in this study display Tl isotopic compositions indistinguishable from our laboratory standard, the reference material NIST-997 Tl. A third sample, however, is characterized by ɛ Tl ≈ 2.5 ± 1.5, where ɛ Tl represents the deviation of the 205Tl/ 203Tl ratio of the sample relative to NIST-997 Tl in parts per 10 4. Even larger deviations were identified for two ferromanganese crusts from the Pacific Ocean, which display ɛ Tl-values of +5.0 ± 1.5 and +11.7 ± 1.3. We suggest that the large variability of Tl isotopic compositions in the latter samples are caused by low-temperature processes related to the formation of the Fe-Mn crusts by precipitation and

Precipitation, groundwater and surface waters. Control of climate parameters on their isotopic composition and their utilization as palaeoclimatological tools

International Nuclear Information System (INIS)

Gat, J.R.

1983-01-01

The isotopic composition of precipitation is correlated with climatic parameters such as mean temperature and humidity both in the source areas of the atmospheric moisture and along the storm trajectories. However, additional meteorological variables such as seasonal distributions of rainfall, convection patterns in the cloud and intensity, duration and intermittency of rain influence the isotopic composition. It is shown in this context that the isotopic composition of Negev and Sinai palaeowaters is consistent with the notion of summer rains in this area arising from Atlantic-based storm centres. (author)

$\\beta$-delayed neutron spectroscopy of $^{130-132}$ Cd isotopes with the ISOLDE decay station and the VANDLE array

CERN Multimedia

We propose to use the new ISOLDE decay station and the neutron detector VANDLE to measure the $\\beta$-delayed neutron emission of N=82-84 $^{130-132}$Cd isotopes. The large delayed neutron emission probability observed in a previous ISOLDE measurement is indicative of the Gamow-Teller transitions due to the decay of deep core neutrons. Core Gamow-Teller decay has been experimentally proven in the $^{78}$Ni region for the N>50 nuclei using the VANDLE array. The spectroscopic measurement of delayed neutron emission along the cadmium isotopic chain will allow us to track the evolution of the single particle states and the shell gap.

Synthesis of Graphene-CdSe Composite by a Simple Hydrothermal Method and Its Photocatalytic Degradation of Organic Dyes

Institute of Scientific and Technical Information of China (English)

OH Won-Chun; CHEN Mingliang; CHO Kwangyoun; KIM Cheolkyu; MENG Zeda; ZHULei

2011-01-01

A graphene-CdSe composite was synthesized by a facile hydrothermal method,and characterized by X-ray diffiraction,scanning electron microscopy with energy dispersive X-ray analysis,transmission electron microscopy and UV-vis diffuse reflectance spectrophotometry.The graphene-CdSe composite efficiently catalyzed the photodegradation of methylene blue (MB),methyl orange (MO) and rhodamine B (Rh.B) in aqueous solution under UV or visible light irradiation.The graphene-CdSe composite exhibited a higher photocatalytic activity for the MB solution.

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.

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.

Thermal stability of substitutional ag in CdTe

NARCIS (Netherlands)

Jahn, SG; Hofsass, H; Restle, M; Ronning, C; Quintel, H; BharuthRam, K; Wahl, U

The thermal stability of substitutional Ag in CdTe was deduced from lattice location measurements at different temperatures. Substitutional Ag probe atoms were generated via transmutation doping from radioactive Cd isotopes. The lattice sites of Ag isotopes were determined by measuring the

Non-traditional Stable Isotope Systematics of Seafloor Hydrothermal Systems

Science.gov (United States)

Rouxel, O. J.

2009-05-01

Seafloor hydrothermal activity at mid-ocean ridges is one of the fundamental processes controlling the chemistry of the oceans and the altered oceanic crust. Past studies have demonstrated the complexity and diversity of seafloor hydrothermal systems and have highlighted the importance of subsurface environments in controlling the composition of hydrothermal fluids and mineralization types. Traditionally, the behavior of metals in seafloor hydrothermal systems have been investigated by integrating results from laboratory studies, theoretical models, mineralogy and fluid and mineral chemistry. Isotope ratios of various metals and metalloids, such as Fe, Cu, Zn, Se, Cd and Sb have recently provided new approaches for the study of seafloor hydrothermal systems. Despite these initial investigations, the cause of the isotopic variability of these elements remains poorly constrained. We have little understanding of the isotope variations between vent types (black or white smokers) as well as the influence of source rock composition (basalt, felsic or ultrabasic rocks) and alteration types. Here, I will review and present new results of metal isotope systematics of seafloor hydrothermal systems, in particular: (1) determination of empirical isotope fractionation factors for Zn, Fe and Cu-isotopes through isotopic analysis of mono-mineralic sulfide grains lining the internal chimney wall in contact with hydrothermal fluid; (2) comparison of Fe- and Cu-isotope signatures of vent fluids from mid- oceanic and back-arc hydrothermal fields, spanning wide ranges of pH, temperature, metal concentrations and contributions of magmatic fluids enriched in SO2. Ultimately, the use of complementary non-traditional stable isotope systems may help identify and constrain the complex interactions between fluids,minerals, and organisms in seafloor hydrothermal systems.

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)

Preparation of CdS@CeO{sub 2} core/shell composite for photocatalytic reduction of CO{sub 2} under visible-light irradiation

Energy Technology Data Exchange (ETDEWEB)

Ijaz, Sana [CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing 100190 (China); Institute of Chemical Sciences, Bahauddin Zakaryia University, Multan 60800 (Pakistan); Ehsan, Muhammad Fahad [CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing 100190 (China); Ashiq, Muhammad Naeem, E-mail: naeemashiqqau@yahoo.com [Institute of Chemical Sciences, Bahauddin Zakaryia University, Multan 60800 (Pakistan); Karamat, Nazia [Institute of Chemical Sciences, Bahauddin Zakaryia University, Multan 60800 (Pakistan); He, Tao, E-mail: het@nanoctr.cn [CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing 100190 (China); University of Chinese Academy of Sciences, Beijing 100049 (China)

2016-12-30

Highlights: • CdS@CeO{sub 2}core(*)/shell composite is fabricated using a two-step method. • CdS@CeO{sub 2} can photoreduce CO{sub 2} into CH{sub 4} and CH{sub 3}OH under visible-light irradiation. • CdS@CeO{sub 2} can enhance photocatalytic activity due to increased charge separation. • Core shell strategy for photocatalyst preparation can improve photostability. - Abstract: Present work demonstrates fabrication of CdS@CeO{sub 2} core/shell composite and its application in the photocatalytic reduction of CO{sub 2} under visible-light irradiation (λ ≥ 420 nm). CdS@CeO{sub 2} composite has been successfully prepared by two-step chemical method, while CeO{sub 2} and CdS have been synthesized by one-step hydrothermal method. X-ray diffraction analysis confirms the formation of fluorite cubic structure of CeO{sub 2} and cubic phase of CdS. High resolution transmission electron microscopy and scanning electron microscopy reveal the microsphere morphology of CdS, while CeO{sub 2} (shell) is in the form of spherical particles that surround the CdS (core) in case of the composite. X-ray photoelectron spectroscopy has been used to confirm the composition, oxidation state of the elements and valance band of the obtained materials. The CdS@CeO{sub 2} core/shell composite and CdS can convert CO{sub 2} into methane and methanol under visible-light irradiation. The CdS@CeO{sub 2} composite shows higher yield for both methane and methanol than CdS due to low recombination rate of photogenerated electron/hole pairs, as well as a larger BET specific surface area. Moreover, the CdS@CeO{sub 2} core/shell composite also shows improved stability upon photocatalysis.

Magnetite/CdTe magnetic-fluorescent composite nanosystem for magnetic separation and bio-imaging

International Nuclear Information System (INIS)

Kale, Anup; Yadav, Prasad; Gholap, Haribhau; Jog, J P; Ogale, Satishchandra; Kale, Sonia; Shastry, Padma; Pasricha, Renu; Lefez, Benoit; Hannoyer, Beatrice

2011-01-01

A new synthesis protocol is described to obtain a CdTe decorated magnetite bifunctional nanosystem via dodecylamine (DDA) as cross linker. High resolution transmission electron microscopy (HRTEM), energy-dispersive x-ray spectroscopy (EDAX), vibrating sample magnetometry (VSM), Fourier transform infrared spectroscopy (FTIR), diffuse reflectance spectroscopy (DRS) and fluorescence microscopy are used to characterize the constitution, size, composition and physical properties of these superparamagnetic-fluorescent nanoparticles. These CdTe decorated magnetite nanoparticles were then functionalized with anti-epidermal growth factor receptor (EGFR) antibody to specifically target cells expressing this receptor. The EGFR is a transmembrane glycoprotein and is expressed on tumor cells from different tissue origins including human leukemic cell line Molt-4 cells. The magnetite-CdTe composite nanosystem is shown to perform excellently for specific selection, magnetic separation and fluorescent detection of EGFR positive Molt-4 cells from a mixed population. Flow cytometry and confocal laser scanning microscopy results show that this composite nanosystem has great potential in antibody functionalized magnetic separation and imaging of cells using cell surface receptor antibody.

Surface complexation modeling of Cd(II) sorption to montmorillonite, bacteria, and their composite

Science.gov (United States)

Wang, Ning; Du, Huihui; Huang, Qiaoyun; Cai, Peng; Rong, Xingmin; Feng, Xionghan; Chen, Wenli

2016-10-01

Surface complexation modeling (SCM) has emerged as a powerful tool for simulating heavy metal adsorption processes on the surface of soil solid components under different geochemical conditions. The component additivity (CA) approach is one of the strategies that have been widely used in multicomponent systems. In this study, potentiometric titration, isothermal adsorption, zeta potential measurement, and extended X-ray absorption fine-structure (EXAFS) spectra analysis were conducted to investigate Cd adsorption on 2 : 1 clay mineral montmorillonite, on Gram-positive bacteria Bacillus subtilis, and their mineral-organic composite. We developed constant capacitance models of Cd adsorption on montmorillonite, bacterial cells, and mineral-organic composite. The adsorption behavior of Cd on the surface of the composite was well explained by CA-SCM. Some deviations were observed from the model simulations at pH SCM closely coincided with the estimated value of EXAFS at pH 6. The model could be useful for the prediction of heavy metal distribution at the interface of multicomponents and their risk evaluation in soils and associated environments.

The effect of natural weathering on the chemical and isotopic composition of biotites

International Nuclear Information System (INIS)

Clauer, N.; Bonnot-Courtois, C.

1982-01-01

The effect of progressive natural weathering on the isotopic (Rb-Sr, K-Ar, deltaD, delta 18 O) and chemical (REE, H 2 O + ) compositions of biotite has been studied on a suite of migmatitic biotites from the Chad Republic. During the early stages of weathering the Rb-Sr system is strongly affected, the hydrogen and oxygen isotope compositions change markedly, the minerals are depleted in light REE, the water content increases by a factor of two, and the K-Ar system is relatively little disturbed. During intensive weathering the K-Ar system is more strongly disturbed than the Rb-Sr system. Most of the isotopic and chemical modifications take place under nonequilibrium conditions and occur before newly formed kaolinite and/or smectite can be detected. These observations suggest that (a) 'protominerals' may form within the biotite structure during the initial period of weathering, and (b) only when chemical equilibrium is approached in the weathering profile are new minerals able to form. (author)

Surface-biofunctionalized multicore/shell CdTe@SiO2 composite particles for immunofluorescence assay

Science.gov (United States)

Jing, Lihong; Li, Yilin; Ding, Ke; Qiao, Ruirui; Rogach, Andrey L.; Gao, Mingyuan

2011-12-01

Strongly fluorescent multicore/shell structured CdTe@SiO2 composite particles of ~ 50 nm were synthesized via the reverse microemulsion method by using CdTe quantum dots co-stabilized by thioglycolic acid and thioglycerol. The optical stability of the CdTe@SiO2 composite particles in a wide pH range, under prolonged UV irradiation in pure water, or in different types of physiological buffers was systematically investigated. Towards immunofluorescence assay, both poly(ethylene glycol) (PEG) and carboxyl residues were simultaneously grafted on the surface of the silanol-terminated CdTe@SiO2 composite particles upon further reactions with silane reagents bearing a PEG segment and carboxyl group, respectively, in order to suppress the nonspecific interactions of the silica particles with proteins and meanwhile introduce reactive moieties to the fluorescent particles. Agarose gel electrophoresis, dynamic light scattering and conventional optical spectroscopy were combined to investigate the effectiveness of the surface modifications. Via the surface carboxyl residue, various antibodies were covalently conjugated to the fluorescent particles and the resultant fluorescent probes were used in detecting cancer cells through both direct fluorescent antibody and indirect fluorescent antibody assays, respectively.

Free-standing optoelectronic graphene-CdS-graphene oxide composite paper produced by vacuum-assisted self-assembly

Energy Technology Data Exchange (ETDEWEB)

Li, Yong-Feng [Chinese Academy of Sciences, Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Taiyuan (China); Graduate University of Chinese Academy of Sciences, Beijing (China); Liu, Yan-Zhen; Shen, Wen-Zhong; Yang, Yong-Gang; Wang, Mao-Zhang [Chinese Academy of Sciences, Key Laboratory of Carbon Materials, Institute of Coal Chemistry, Taiyuan (China); Wen, Yue-Fang [Zhejiang University, Department of Chemical and Biological Engineering, Hangzhou (China)

2012-03-15

Free-standing optoelectronic graphene-CdS-graphene oxide (G-CdS-GO) composite papers were prepared by vacuum-assisted self-assembly. G-CdS hybrids were first prepared by a hydrothermal method and GO acts as a dispersant which makes it easier to disperse them to form relatively stable aqueous suspensions for fabricating paper. Transmission electron microscopy shows that CdS quantum dots (QDs) with an average size of approximately 1-2 nm were distributed uniformly on the graphene sheets. Photoluminescence measurements for the as-prepared G-CdS-GO composite paper showed that the surface defect related emissions of attached CdS QDs decrease and blue shift obviously due to the change in particle size and the interaction of the surface of the CdS QDs with both the GO and the graphene sheets. The resulting paper holds great potential for applications in thin film solar cells, sensors, diodes, and so on. (orig.)

Reassessment of the NH4 NO3 thermal decomposition technique for calibration of the N2 O isotopic composition.

Science.gov (United States)

Mohn, Joachim; Gutjahr, Wilhelm; Toyoda, Sakae; Harris, Eliza; Ibraim, Erkan; Geilmann, Heike; Schleppi, Patrick; Kuhn, Thomas; Lehmann, Moritz F; Decock, Charlotte; Werner, Roland A; Yoshida, Naohiro; Brand, Willi A

2016-09-08

In the last few years, the study of N 2 O site-specific nitrogen isotope composition has been established as a powerful technique to disentangle N 2 O emission pathways. This trend has been accelerated by significant analytical progress in the field of isotope-ratio mass-spectrometry (IRMS) and more recently quantum cascade laser absorption spectroscopy (QCLAS). Methods The ammonium nitrate (NH 4 NO 3 ) decomposition technique provides a strategy to scale the 15 N site-specific (SP ≡ δ 15 N α - δ 15 N β ) and bulk (δ 15 N bulk  = (δ 15 N α  + δ 15 N β )/2) isotopic composition of N 2 O against the international standard for the 15 N/ 14 N isotope ratio (AIR-N 2 ). Within the current project 15 N fractionation effects during thermal decomposition of NH 4 NO 3 on the N 2 O site preference were studied using static and dynamic decomposition techniques. The validity of the NH 4 NO 3 decomposition technique to link NH 4 + and NO 3 - moiety-specific δ 15 N analysis by IRMS to the site-specific nitrogen isotopic composition of N 2 O was confirmed. However, the accuracy of this approach for the calibration of δ 15 N α and δ 15 N β values was found to be limited by non-quantitative NH 4 NO 3 decomposition in combination with substantially different isotope enrichment factors for the conversion of the NO 3 - or NH 4 + nitrogen atom into the α or β position of the N 2 O molecule. The study reveals that the completeness and reproducibility of the NH 4 NO 3 decomposition reaction currently confine the anchoring of N 2 O site-specific isotopic composition to the international isotope ratio scale AIR-N 2 . The authors suggest establishing a set of N 2 O isotope reference materials with appropriate site-specific isotopic composition, as community standards, to improve inter-laboratory compatibility. This article is protected by copyright. All rights reserved.

Composition determination of CdSxSe1-x mixed crystals by optical dispersion

International Nuclear Information System (INIS)

Iliev, I.; Dimov, T.; Ribarov, D.; Lange, H.

1989-01-01

An optical dispersion method has been developed determining the CdS/CdSe ratio in CdS x Se 1-x mixed crystals from the relationship between position of the isotropic point (birefrigence becomes zero for a definite wavelength at the absorption edge) and chemical composition x. Birefrigence spectra and piezo-optic spectra of samples with x = 0.2, 0.6, and 0.875 give the spectral position of the isotropic point (ip). A curve of wavelength of ip versus x of CdS x Se 1-x is evaluated by the least-squares procedure and tested by X-ray fluorescence analysis

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.

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...

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"1"5N and δ"1"8O 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

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

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...

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

Isotopic composition of water in precipitation due to seasonal variation and variation in intensity of rain fall at a place

International Nuclear Information System (INIS)

Singh, B.P.

2015-01-01

An attempt has been made to analyze the data to find the original precipitate on GMWL, when there is seasonal variation and variations in intensity of rain fall at the same longitude, latitude and altitude. This has been done using the data as available for each month, weighted average of month and individual year for δ 2 H and δ 18 O for a 10-year periods. Correlation equations between δ 2 H and δ 18 O are available giving slopes and intercepts on the δ 2 H axis for 10-year periods. The data of slope versus intercept for each month, weighted monthly average value and individual year are plotted to arrive at isotope composition of meteoric water δ 18 O and δ 2 H, the method suggested by (Singh B.P. 2013, Isotopic composition of water in precipitation in a region or place, Applied Radiation and Isotopes, vol. 75, pp. 22–25; Singh B.P. 2014, Isotopic composition of river water across a continent, Applied Radiation and Isotopes, vol. 85, pp. 14–18). The results of the original meteoric isotopic composition of water are within the experimental errors as analyzed on a yearly basis, the average of each month of yearly basis and on the basis of each month and also some different amounts of precipitation giving the same value of δ 18 O=−16.72 and δ 2 H=−129.86 on GMWL. - Highlights: • New pattern, plot of slope versus intercept between δ 18 O and δ 2 H at the same location for seasons and rainfall are given. • These patterns are analyzed to arrive at the original isotopic composition to be on GMWL. • It is found that the original isotopic composition is same for different seasons and amount of rainfall

Hydrochemical and Isotopic Assessment of Ground Water in Eastern Desert, Egypt

International Nuclear Information System (INIS)

Atiti, S.Y.; Ali, M.M.; Yousef, L.A.; Dessouki, H.A.

2011-01-01

The recharge rate is the most critical factor to ground water resources especially in semi- arid and arid areas. Fourteen representative ground water samples were collected from South Eastern Desert of Egypt and subjected to chemical and isotopic composition. The chemical data reported that, the alkalinity (ph) ranges between 6.5 and 8.5, the salinity of water ranges between 396 and 7874 ppm, sodium is the most dominant cation and chloride is the most dominant anion. The concentration of trace elements (Fe, Pb, Cd, Ni, Cu, Zn, and Mn) was analyzed to evaluate the suitability for drinking and irrigation. Uranium and thorium concentrations were found within the safe limit. Most of ground water was found suitable for drinking water, laundry, irrigation, building, industrial, livestock and poultry. The environmental stable isotopes (D and 18 O) and the radioactive isotope 3 H were evaluated for water samples of the investigated area to focus on the origin of the ground water, sources of recharging and the water rock interaction between aquifers and water. The isotopic compositions of these ground water samples indicated that, there are three different sources of recharge; paleo-water, local precipitation and rain water

Containing arsenic-enriched groundwater tracing lead isotopic compositions of common arsenical pesticides in a coastal Maine watershed

Science.gov (United States)

Ayuso, Robert A.; Foley, Nora K.; Robinson, Glipin R.; Colvin, A.S.; Lipfert, G.; Reeve, A.S.

2006-01-01

Arsenical pesticides and herbicides were extensively used on apple, blueberry, and potato crops in New England during the first half of the twentieth century. Lead arsenate was the most heavily used arsenical pesticide until it was officially banned. Lead arsenate, calcium arsenate, and sodium arsenate have similar Pb isotope compositions: 208Pb207Pb = 2.3839-2.4722, and 206Pb207Pb = 1.1035-1.2010. Other arsenical pesticides such as copper acetoarsenite (Paris green), methyl arsonic acid and methane arsonic acid, as well as arsanilic acid are widely variable in isotope composition. Although a complete understanding of the effects of historical use of arsenical pesticides is not available, initial studies indicate that arsenic and lead concentrations in stream sediments in New England are higher in agricultural areas that intensely used arsenical pesticides than in other areas. The Pb isotope compositions of pesticides partially overlap values of stream sediments from areas with the most extensive agricultural use. The lingering effects of arsenical pesticide use were tested in a detailed geochemical and isotopic study of soil profiles from a watershed containing arsenic-enriched ground water in coastal Maine. Acid-leach compositions of the soils represent lead adsorbed to mineral surfaces or held in soluble minerals (Fe- and Mn-hydroxides, carbonate, and some micaceous minerals), whereas residue compositions likely reflect bedrock compositions. The soil profiles contain labile Pb (acid-leach) showing a moderate range in 206Pb 207Pb (1.1870-1.2069), and 208Pb207Pb (2.4519-2.4876). Isotope values vary as a function of depth: the lowest Pb isotope ratios (e.g.,208Pb206Pb) representing labile lead are in the uppermost soil horizons. Lead contents decrease with depth in the soil profiles. Arsenic contents show no clear trend with depth. A multi-component mixing scheme that included lead from the local parent rock (Penobscot Formation), lead derived from combustion of

The Effect of Phytase on the Oxygen Isotope Composition of Phosphate

Science.gov (United States)

von Sperber, C.; Tamburini, F.; Bernasconi, S. M.; Frossard, E.

2013-12-01

Plants and microorganisms under phosphorus (P) stress release extracellular phosphatases as a strategy to acquire inorganic phosphate (Pi) (1-2). These enzymes catalyze the hydrolysis of phosphoesters leading to a release of Pi. The enzymatic hydrolysis leads, via a nucleophilic attack, to the incorporation of one oxygen atom from the water into the newly formed Pi molecule. During the incorporation, an isotopic fractionation occurs, which might be used to identify the origin of Pi in the environment (3-6). While the effect of phosphomonoesterases and phosphodiesterases on the oxygen isotope composition of phosphate has been examined, there are, so far, no studies dealing with the effect of phytases (4-6). Phytases catalyze the hydrolysis of myo-inositol-hexakis-phosphate (IP6), which is an important component of organic P in many ecosystems (7). Enzymatic assays with phytase from wheat germ and Aspergillus niger were prepared under sterile and temperature controlled conditions in order to determine the effect of phytases on the oxygen isotope composition of phosphate, which has been liberated from IP6 via enzymatic hydrolysis. Assays with phytase from wheat germ lead to a turnover of the substrate close to 100%, while assays with phytase from Aspergillus niger lead to a turnover of the substrate close to 80%. In the case of the assays with phytase from wheat germ, our results indicate that one sixth of the total 24 oxygen which are associated to the phosphates in IP6 are exchanged with oxygen from water. From this we conclude that the incorporation of one oxygen atom from water occurs only at four phosphate molecules of IP6, while two phosphate molecules do not experience an incorporation of oxygen. This suggests that during the enzymatic hydrolysis, four P-O bonds and two C-O bonds are broken. Provided that, the isotopic fractionation can be calculated with an isotopic mass balance resulting in -8.4‰ (×3.6 SD). This is a value very similar to those reported

Fabrication of titanate nanotubes/iron oxide magnetic composite for the high efficient capture of radionuclides: a case investigation of 109Cd(II)

International Nuclear Information System (INIS)

Lei Dai; Jun Zheng; Lijie Wang

2013-01-01

In this paper, the capture of radiocadmium (Cd(II)) by adsorption onto the titanate nanotube/iron oxide (TNT/IOM) magnetic composite as a function of contact time, pH, ionic strength, foreign cation and anion ions, humic acid (HA) and fulvic acid (FA) was studied using batch technique. The results indicated that the adsorption of Cd(II) onto the TNT/IOM magnetic composite was dependent on ionic strength at pH 9.0. Outer-sphere surface complexation were the main mechanism of Cd(II) adsorption onto the TNT/IOM magnetic composite at low pH values, whereas the adsorption was mainly dominated via inner-sphere surface complexation at high pH values. The adsorption of Cd(II) onto the TNT/IOM magnetic composite was dependent on foreign cation and anion ions at low pH values, but was independent of foreign cation and anion ions at high pH values. A positive effect of HA/FA on Cd(II) adsorption onto the TNT/IOM magnetic composite was found at low pH values, while a negative effect was observed at high pH values. From the results of Cd(II) removal by the TNT/IOM magnetic composite, the optimum reaction conditions can be obtained for the maximum removal of Cd(II) from water. It is clear that the best pH values of the system to remove Cd(II) from solution by using the TNT/IOM magnetic composite are 7.0-8.0. Considering the low cost and effective disposal of Cd(II)-contaminated wastewaters, the best condition for Cd(II) capture by the TNT/IOM magnetic composite is at room temperature and solid content of 0.5 g L -1 . These results are quite important for estimating and optimizing the removal of Cd(II) and related metal ions by the TNT-based magnetic composite. (author)

Isotope composition of winter precipitation and snow cover in the foothills of the Altai

Directory of Open Access Journals (Sweden)

N. S. Malygina

2017-01-01

Full Text Available Over the past three decades, several general circulation models of the atmosphere and ocean (atmospheric and oceanic general circulation models  – GCMs have been improved by modeling the hydrological cycle with the use of isotopologues (isotopes of water HDO and H2 18O. Input parameters for the GCM models taking into account changes in the isotope composition of atmospheric precipitation were, above all, the results obtained by the network GNIP – Global Network of Isotopes in Precipitation. At different times, on the vast territory of Russia there were only about 40 simultaneously functioning stations where the sampling of atmospheric precipitation was performed. In this study we present the results of the isotope composition of samples taken on the foothills of the Altai during two winter seasons of 2014/15 and 2015/16. Values of the isotope composition of precipitation changed in a wide range and their maximum fluctuations were 25, 202 and 18‰ for δ18О, dexc and δD, respectively. The weighted-mean values of δ18О and δD of the precipitation analyzed for the above two seasons were close to each other (−21.1 and −158.1‰ for the first season and −21.1 and −161.9‰ for the second one, while dexc values differed significantly. The comparison of the results of isotope analysis of the snow cover integral samples with the corresponding in the time interval the weighted-mean values of precipitation showed high consistency. However, despite the similarity of values of δ18О and δD, calculated for precipitation and snow cover, and the results, interpolated in IsoMAP (from data of the GNIP stations for 1960–2010, the dexc values were close to mean annual values of IsoMAP for only the second winter season. According to the trajectory analysis (the HYSPLIT model, the revealed differences between both, the seasons, and the long-term average values of IsoMAP, were associated with a change of main regions where the air masses

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

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

The silicon isotopic composition of fine-grained river sediments and its relation to climate and lithology

Science.gov (United States)

Bayon, G.; Delvigne, C.; Ponzevera, E.; Borges, A. V.; Darchambeau, F.; De Deckker, P.; Lambert, T.; Monin, L.; Toucanne, S.; André, L.

2018-05-01

The δ30Si stable isotopic composition of silicon in soils and fine-grained sediments can provide insights into weathering processes on continents, with important implications on the Si budget of modern and past oceans. To further constrain the factors controlling the distribution of Si isotopes in sediments, we have analysed a large number (n = 50) of separate size-fractions of sediments and suspended particulate materials collected near the mouth of rivers worldwide. This includes some of the world's largest rivers (e.g. Amazon, Congo, Mackenzie, Mississippi, Murray-Darling, Nile, Yangtze) and rivers from the case study areas of the Congo River Basin and Northern Ireland. Silt-size fractions exhibit a mean Si isotopic composition (δ30Si = -0.21 ± 0.19‰; 2 s.d.) similar to that previously inferred for the upper continental crust. In contrast, clay-size fractions display a much larger range of δ30Si values from -0.11‰ to -2.16‰, which yield a global δ30Siclay of -0.57 ± 0.60‰ (2 s.d.) representative of the mean composition of the average weathered continental crust. Overall, these new data show that the Si isotopic signature transported by river clays is controlled by the degree of chemical weathering, as inferred from strong relationships with Al/Si ratios. At a global scale, the clay-bound Si isotopic composition of the world's largest river systems demonstrates a link with climate, defining a general correlation with mean annual temperature (MAT) in corresponding drainage basins. While the distribution of Si isotopes in river sediments also appears to be influenced by the tectonic setting, lithological effects and sediment recycling from former sedimentary cycles, our results pave the way for their use as paleo-weathering and paleo-climate proxies in the sedimentary record.

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

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.

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...

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

Permafrost hydrology in changing climatic conditions: seasonal variability of stable isotope composition in rivers in discontinuous permafrost

International Nuclear Information System (INIS)

Streletskiy, Dmitry A; Shiklomanov, Nikolay I; Nyland, Kelsey E; Tananaev, Nikita I; Opel, Thomas; Streletskaya, Irina D; Tokarev, Igor’; Shiklomanov, Alexandr I

2015-01-01

Role of changing climatic conditions on permafrost degradation and hydrology was investigated in the transition zone between the tundra and forest ecotones at the boundary of continuous and discontinuous permafrost of the lower Yenisei River. Three watersheds of various sizes were chosen to represent the characteristics of the regional landscape conditions. Samples of river flow, precipitation, snow cover, and permafrost ground ice were collected over the watersheds to determine isotopic composition of potential sources of water in a river flow over a two year period. Increases in air temperature over the last forty years have resulted in permafrost degradation and a decrease in the seasonal frost which is evident from soil temperature measurements, permafrost and active-layer monitoring, and analysis of satellite imagery. The lowering of the permafrost table has led to an increased storage capacity of permafrost affected soils and a higher contribution of ground water to river discharge during winter months. A progressive decrease in the thickness of the layer of seasonal freezing allows more water storage and pathways for water during the winter low period making winter discharge dependent on the timing and amount of late summer precipitation. There is a substantial seasonal variability of stable isotopic composition of river flow. Spring flooding corresponds to the isotopic composition of snow cover prior to the snowmelt. Isotopic composition of river flow during the summer period follows the variability of precipitation in smaller creeks, while the water flow of larger watersheds is influenced by the secondary evaporation of water temporarily stored in thermokarst lakes and bogs. Late summer precipitation determines the isotopic composition of texture ice within the active layer in tundra landscapes and the seasonal freezing layer in forested landscapes as well as the composition of the water flow during winter months. (letter)

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

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)

What is the effect of variations optimization of the transition state on α-deuterium secondary kinetic isotope effects? A prototype: CD3H + H right-reversible CD3 + H2

International Nuclear Information System (INIS)

Lu, Dahong; Maurice, D.; Truhlar, D.G.

1990-01-01

Variational Transition state theory calculations with semiclassical transmission coefficients have been carried out for a prototype case of α-deuterium secondary kinetic isotope effects (KIEs) in a reaction involving the transformation of an sp 3 carbon to sp 2 , in particular for the reactions of CH 4 and CD 3 H with H and D. The authors also study the KIE for the reverse direction and for the reactions of CH 4 and CD 3 H with D. They find that the variational transition states lead to significantly different nontunneling KIEs than the conventional ones, e.g., 1.22 vs. 1.07, and the inclusion of multidimensional tunneling effects increases the discrepancy even more. The origins of these variations and tunneling effects are examined in detail in terms of structures, vibrational frequencies, and the curvature of the reaction path. The conclusions have wide implications for the validity of conventional treatments of kinetic isotope effects. They predict some particularly large secondary KIEs at low temperature, and these predictions can be tested by future experiments

CdS nanoparticles/CeO{sub 2} nanorods composite with high-efficiency visible-light-driven photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

You, Daotong; Pan, Bao; Jiang, Fan; Zhou, Yangen; Su, Wenyue, E-mail: suweny@fzu.edu.cn

2016-02-15

Graphical abstract: Coupling CdS with CeO{sub 2} can effectively improve the light-harvesting ability of wide-band gap CeO{sub 2} NRs as the photoinduced electrons on the conduction band of CdS are transfered to the conduction band of CeO{sub 2}. - Highlights: • Coupling CdS can effectively improve the light-harvesting ability of wide-band gap CeO{sub 2}. • CdS/CeO{sub 2} composites show high photocatalytic activity under visible light irradiation. • The mechanism of photocatalytic H{sub 2} evolution over CdS/CeO{sub 2} was proposed. - Abstract: Different mole ratios of CdS nanoparticles (NPs)/CeO{sub 2} nanorods (NRs) composites with effective contacts were synthesized through a two-step hydrothermal method. The crystal phase, microstructure, optical absorption properties, electrochemical properties and photocatalytic H{sub 2} production activity of these composites were investigated. It was concluded that the photogenerated charge carriers in the CdS NPs/CeO{sub 2} NRs composite with a proper mole ratio (1:1) exhibited the longest lifetime and highest separation efficiency, which was responsible for the highest H{sub 2}-production rate of 8.4 mmol h{sup −1} g{sup −1} under visible-light irradiation (λ > 420 nm). The superior photocatalytic H{sub 2} evolution properties are attributed to the transfer of visible-excited electrons of CdS NPs to CeO{sub 2} NRs, which can effectively extend the light absorption range of wide-band gap CeO{sub 2} NRs. This work provides feasible routes to develop visible-light responsive CeO{sub 2}-based nanomaterial for efficient solar utilization.

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)

Monte-Carlo code calculation of 3D reactor core model with usage of burnt fuel isotopic compositions, obtained by engineering codes

Energy Technology Data Exchange (ETDEWEB)

Aleshin, Sergey S.; Gorodkov, Sergey S.; Shcherenko, Anna I. [National Research Centre ' Kurchatov Institute' , Moscow (Russian Federation)

2016-09-15

A burn-up calculation of large systems by Monte-Carlo code (MCU) is complex process and it requires large computational costs. Previously prepared isotopic compositions are proposed to be used for the Monte-Carlo code calculations of different system states with burnt fuel. Isotopic compositions are calculated by an approximation method. The approximation method is based on usage of a spectral functionality and reference isotopic compositions, that are calculated by the engineering codes (TVS-M, BIPR-7A and PERMAK-A). The multiplication factors and power distributions of FAs from a 3-D reactor core are calculated in this work by the Monte-Carlo code MCU using earlier prepared isotopic compositions. The separate conditions of the burnt core are observed. The results of MCU calculations were compared with those that were obtained by engineering codes.

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.

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.

Using semi-continuous, in-situ measurements of nitrous oxide isotopic composition at a suburban site to track emission processes

Science.gov (United States)

Harris, Eliza; Henne, Stephan; Christoph, Hüglin; Christoph, Zellweger; Béla, Tuzson; Erkan, Ibraim; Lukas, Emmenegger; Joachim, Mohn

2017-04-01

Nitrous oxide (N2O) is a potent greenhouse gas and the strongest ozone-destroying substance emitted this century. The atmospheric N2O mole fraction has been increasing at a rate of 0.2-0.3% per year over the past decades due to anthropogenic emissions; in addition, recent results suggest that the rate of increase is rising - therefore effective mitigation of N2O emissions is a critical point for environmental policy. However, N2O sources are poorly defined and disperse, complicating the development of targeted mitigation strategies. Online isotopic measurements using preconcentration and laser spectroscopy [1,2,3] have great potential to unravel spatial and temporal variations in sources, sinks and chemistry of trace gases such as N2O. Semi-continuous, real-time measurements of N2O isotopic composition (δ18O, site preference [SP = 14N15N16O - 15N14N16O] and δ15Nbulk) were performed at the suburban site of Dübendorf, Switzerland, for 19 months between July 2014 and February 2016. The data precision reached 0.1‰ in the final months, thus the results could clearly identify nocturnal build-up of N2O, with a corresponding decrease in δ18O, SP and δ15Nbulk due to isotopically depleted anthropogenic sources. Daily mean source isotopic composition was calculated by considering the measured and the background mole fraction and isotopic composition. Delta values of the mean emission source were highest in winter, with a seasonal cycle of 12, 8 and 5‰ for δ18O, SP and δ15Nbulk respectively. The chemical and meteorological parameters controlling source isotopic composition were considered using data from the Swiss National Air Pollution Monitoring Network (NABEL) as well as a transport regime cluster analysis. A clear spatial distribution for source isotopic composition was observed for δ18O, as well as a significant relationship with the level of urban pollution, indicating δ18O may be a strong indicator of combustion/industrial vs. agricultural N2O. In contrast

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.

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.

Carbon isotopic composition of legumes with photosynthetic stems from Mediterranean and desert habitats

International Nuclear Information System (INIS)

Nilsen, E.T.; Sharifi, M.R.

1997-01-01

The carbon isotopic compositions of leaves and stems of woody legumes growing in coastal mediterranean and inland desert sites in California were compared. The overall goal was to determine what factors were most associated with the carbon isotope composition of photosynthetic stems in these habitats. The carbon isotope signature (delta 13C) of photosynthetic stems was less negative than that of leaves on the same plants by an average of 1.51 +/- 0.42 per thousand. The delta 13C of bark (cortical chlorenchyma and epidermis) was more negative than that of wood (vascular tissue and pith) from the same plant for all species studied on all dates. Desert woody legumes had a higher delta 13C (less negative) and a lower intercellular CO2 concentration (Ci) (for both photosynthetic tissues) than that of woody legumes from mediterranean climate sites. Differences in the delta 13C of stems among sites could be entirely accounted for by differences among site air temperatures. Thus, the delta 13C composition of stems did not indicate a difference in whole-plant integrated water use efficiency (WUE) among sites. In contrast, stems on all plants had a lower stem Ci and a higher delta 13C than leaves on the same plant, indicating that photosynthetic stems improve long-term, whole-plant water use efficiency in a diversity of species

In situ observations of the isotopic composition of methane at the Cabauw tall tower site

Directory of Open Access Journals (Sweden)

T. Röckmann

2016-08-01

Full Text Available High-precision analyses of the isotopic composition of methane in ambient air can potentially be used to discriminate between different source categories. Due to the complexity of isotope ratio measurements, such analyses have generally been performed in the laboratory on air samples collected in the field. This poses a limitation on the temporal resolution at which the isotopic composition can be monitored with reasonable logistical effort. Here we present the performance of a dual isotope ratio mass spectrometric system (IRMS and a quantum cascade laser absorption spectroscopy (QCLAS-based technique for in situ analysis of the isotopic composition of methane under field conditions. Both systems were deployed at the Cabauw Experimental Site for Atmospheric Research (CESAR in the Netherlands and performed in situ, high-frequency (approx. hourly measurements for a period of more than 5 months. The IRMS and QCLAS instruments were in excellent agreement with a slight systematic offset of (+0.25 ± 0.04 ‰ for δ13C and (−4.3 ± 0.4 ‰ for δD. This was corrected for, yielding a combined dataset with more than 2500 measurements of both δ13C and δD. The high-precision and high-temporal-resolution dataset not only reveals the overwhelming contribution of isotopically depleted agricultural CH4 emissions from ruminants at the Cabauw site but also allows the identification of specific events with elevated contributions from more enriched sources such as natural gas and landfills. The final dataset was compared to model calculations using the global model TM5 and the mesoscale model FLEXPART-COSMO. The results of both models agree better with the measurements when the TNO-MACC emission inventory is used in the models than when the EDGAR inventory is used. This suggests that high-resolution isotope measurements have the potential to further constrain the methane budget when they are performed at multiple sites that are representative for

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

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

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.

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.

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.)

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.)

Determination of isotopic composition of boron in boron carbide by TIMS and PIGE: an inter-comparison study

International Nuclear Information System (INIS)

Sasibhushan, K.; Rao, R.M.; Parab, A.R.; Alamelu, D.; Aggarwal, S.K.; Acharya, R.; Chhillar, S.; Pujari, P.K.

2015-01-01

The paper reports a comparison of results on the determination of isotopic composition of boron in boron carbide (B 4 C) samples by Thermal Ionisation Mass Spectrometry (TIMS) and Particle Induced Gamma ray Spectrometry (PIGE). B 4 C samples having varying boron isotopic composition (natural, enriched with respect to 10 B) and their synthetic mixtures) have been analysed by both the techniques. The 10 B atom% was found to be in the range of 20-67%. (author)

Isotopic compositions and probable origins of organic molecules in the Eocene Messel shale

Science.gov (United States)

Hayes, J. M.; Takigiku, Ray; Ocampo, Ruben; Callot, Enry J.; Albrecht, Pierre

1987-01-01

It is shown here that the carbon isotopic compositions of biomarkers from the Eocene Messel shale, accumulated 47 + or - 2 million years ago in anaerobic waters at the bottom of a lake, allow identification of specific sources for some materials and reconstruction of carbon flows within the lake and its sediments. The C-13 content of organic matter synthesized by lacustrine primary producers can be estimated from the observed C-13 content of the geoporphyrins derived from their chlorophylls. Total organic material in the shale is depleted in C-13 by six parts per thousand relative to that input. This difference cannot be explained by selective loss of components enriched in C-13, nor, as shown by isotopic compositions of other biomarkers, by inputs from land plants surrounding the lake or from methanogenic bacteria.

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.

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

Amino acid compositions in heated carbonaceous chondrites and their compound-specific nitrogen isotopic ratios

Science.gov (United States)

Chan, Queenie Hoi Shan; Chikaraishi, Yoshito; Takano, Yoshinori; Ogawa, Nanako O.; Ohkouchi, Naohiko

2016-01-01

A novel method has been developed for compound-specific nitrogen isotope compositions with an achiral column which was previously shown to offer high precision for nitrogen isotopic analysis. We applied the method to determine the amino acid contents and stable nitrogen isotopic compositions of individual amino acids from the thermally metamorphosed (above 500 °C) Antarctic carbonaceous chondrites Ivuna-like (CI)1 (or CI-like) Yamato (Y) 980115 and Ornans-like (CO)3.5 Allan Hills (ALH) A77003 with the use of gas chromatography/combustion/isotope ratio mass spectrometry. ALHA77003 was deprived of amino acids due to its extended thermal alteration history. Amino acids were unambiguously identified in Y-980115, and the δ15N values of selected amino acids (glycine +144.8 ‰; α-alanine +121.2 ‰) are clearly extraterrestrial. Y-980115 has experienced an extended period of aqueous alteration as indicated by the presence of hydrous mineral phases. It has also been exposed to at least one post-hydration short-lived thermal metamorphism. Glycine and alanine were possibly produced shortly after the accretion event of the asteroid parent body during the course of an extensive aqueous alteration event and have abstained from the short-term post-aqueous alteration heating due to the heterogeneity of the parent body composition and porosity. These carbonaceous chondrite samples are good analogs that offer important insights into the target asteroid Ryugu of the Hayabusa-2 mission, which is a C-type asteroid likely composed of heterogeneous materials including hydrated and dehydrated minerals.

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.

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

Determination of Cd, Hg, Pb and Se in sediments slurries by isotopic dilution calibration ICP-MS after chemical vapor generation using an on-line system or retention in an electrothermal vaporizer treated with iridium

International Nuclear Information System (INIS)

Vieira, Mariana Antunes; Ribeiro, Anderson Schwingel; Dias, Lucia Felicidade; Curtius, Adilson Jose

2005-01-01

A method for the determination of Cd, Hg, Pb and Se in sediments reference materials by slurry sampling chemical vapor generation (CVG) using isotopic dilution (ID) calibration and detection by inductively coupled plasma mass spectrometry (ICP-MS) is proposed. Two different systems were used for the investigation: an on-line flow injection system (FI-CVG-ICP-MS) and an off-line system with in situ trapping electrothermal vaporization (CVG-ETV-ICP-MS). About 100 mg of the reference material, ground to a particle size ≤50 μm, was mixed with acid solutions (aqua regia, HF and HCl) in an ultrasonic bath. The enriched isotopes 111 Cd, 198 Hg, 206 Pb and 77 Se were then added to the slurry in an adequate amount in order to produce an altered isotopic ratio close to 1. For the on-line system, a standing time for the slurry of 12 h before measurement was required, while for the batch system, no standing time is needed to obtain accurate results. The conditions for the formation of the analyte vapor were optimized for the evaluated systems. The following altered isotope ratios were measured: 111 Cd/ 114 Cd, 198 Hg/ 199 Hg, 206 Pb/ 208 Pb e 77 Se/ 82 Se. The obtained detection limits in the on-line system, in μg g -1 , were: Cd: 0.15; Hg: 0.09; Pb: 6.0 and Se: 0.03. Similar detection limits were obtained with the system that uses the ETV: 0.21 for Hg, 6.0 for Pb and 0.06 μg g -1 for Se. No signal for Cd was obtained in this system. One estuarine, two marine and two river certified sediments were analyzed to check the accuracy. The obtained values by both systems were generally in agreement with the certified concentrations, according to the t-test for a confidence level of 95%, demonstrating that isotope equilibration was attained in the slurries submitted to a chemical vapor generation procedure and detection by ICP-MS. The relative standard deviations were lower than 10%, adequate for slurry analysis. The almost quantitative analytes extractions to the aqueous phase

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...

Kinetic isotope effects in the gas phase reactions of OH and Cl with CH3Cl, CD3Cl, and 13CH3Cl

Directory of Open Access Journals (Sweden)

A. A. Gola

2005-01-01

Full Text Available The kinetic isotope effects in the reactions of CH3Cl, 13CH3Cl and CD3Cl with OH radicals and Cl atoms were studied in relative rate experiments at 298±2 K and 1013±10 mbar. The reactions were carried out in a smog chamber using long path FTIR detection and the spectroscopic data analyzed employing a non-linear least squares spectral fitting method using measured high-resolution infrared spectra as well as absorption cross sections from the HITRAN database. The reaction rates of 13CH3Cl and CD3Cl with OH and Cl were determined relative to CH3Cl as: kOH+CH3ClkOH+CH3Cl/kOH+13CH3Cl}kOH+13CH3Cl=1.059±0.008, kOH+CH3ClkOH+CH3Cl/kOH+CD3ClkOH+CD3Cl=3.9±0.4, kCl+CH3ClkCl+CH3Cl/kCl+13CH3ClkCl+13CH3Cl =1.070±0.010 and kCl+CH3ClkCl+CH3Cl/kCl+CD3ClkCl+CD3Cl=4.91±0.07. The uncertainties given are 2σ from the statistical analyses and do not include possible systematic errors. The unexpectedly large 13C kinetic isotope effect in the OH reaction of CH3Cl has important implications for the global emission inventory of CH3Cl.

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.

Lead isotopic composition of paleozoic and late proterozoic marine carbonate rocks in the vicinity of Yucca Mountains, Nevada

International Nuclear Information System (INIS)

Zartman, R.E.; Kwak, L.M.

1993-01-01

Paleozoic and Late Proterozoic marine carbonate rocks (limestones, dolomites, and their metamorphic equivalents) cropping out in the vicinity of Yucca Mountain contain lead with an isotopic composition strongly suggesting them to be a major source of the lead observed at Trench 14 in the carbonate phase of carbonate-silica veins and nearby surficial calcrete deposits. Six whole-rock samples of marine carbonate rocks yield 206 Pb/ 204 Pb = 19.21-29.06, 207 Pb/ 204 Pb = 15.74-16.01, and 208 Pb/ 204 Pb = 37.90-39.25, and leachate and residue fractions of the rocks reveal additional isotopic heterogeneity within individual samples. Two samples of eolian dust also have isotopic compositions lying along a 'carbonate' to 'silicate' mixing trend that appears to arise entirely from pedeogenic processes. The tendency for the marine carbonate rocks to evolve highly uranogenic, but not thorogenic, lead results in a distinctive isotopic composition that serves as a tracer in eolian dust and secondary carbonate minerals derived from the marine carbonate rocks

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).

Production of the isotope /sup 105/In and investigation of the decay /sup 105/In. -->. /sup 105/Cd

Energy Technology Data Exchange (ETDEWEB)

Rivier, J; Moret, R [Institut des Sciences Nucleaires, 38 - Grenoble (France)

1975-01-01

A new isotope, /sup 105/In, was produced by means of the reaction /sup 106/Cd(p,2n). The half-life of the ground state is 5.1 +- 0.3 min. There is an isomeric level at 674.1 keV (T/sub 1/2/ = 55 +- 5 sec). Thirty-two transitions have been found, and a decay scheme has been set up through a study of the ..gamma.. spectrum and by coincidence techniques.

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.

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

Results of the international Pu-2000 exercise for plutonium isotopic composition measurements

International Nuclear Information System (INIS)

Morel, J.; Bickel, M.; Hill, C.; Verbruggen, A.

2004-01-01

An international comparison for plutonium isotopic composition measurement, known as the Pu-2000 exercise, was organized by the ESARDA NDA-WG (European Safeguards Research and Development Association, Working Group on Techniques and Standards for Non-Destructive Assay). The aim of this comparison was to test X- and γ-ray spectrometry methods over a large range of isotopic ratios. These methods are based on the complex analysis of several X- and γ-rays in the KX region of the plutonium spectrum and also in the 120-700 keV energy range. The results obtained by the participants with their corresponding uncertainties are presented in this document and compared to the declared values. The main conclusions of the work are also given. No important bias due to an inadequate knowledge of the nuclear data for plutonium isotopes was observed

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

Facile preparation of novel organic–inorganic PI/Zn0.25Cd0.75S composite for enhanced visible light photocatalytic performance

International Nuclear Information System (INIS)

Yan, Tao; Li, Mengmeng; Wang, Xiaodong; Sun, Meng; Liu, Hongye; Wei, Qin; Xu, Wenguo; Du, Bin

2015-01-01

Graphical abstract: - Highlights: • Novel PI/Zn 0.25 Cd 0.75 S composite showed enhanced activity in dye degradation. • The composites PIZCS-30 exhibited the best activity. • The heterojunction was in situ fabricated between PI and Zn 0.25 Cd 0.75 S. • The PI/Zn 0.25 Cd 0.75 S heterojunction facilitated the separation of electron–hole pairs. - Abstract: Novel organic–inorganic polyimide (PI)–Zn 0.25 Cd 0.75 S composites with high-efficiency visible light performance was prepared by a facile and template free hydrothermal method. The obtained composites were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photo-electron spectroscopy (XPS), ultraviolet–visible diffuse reflection spectroscopy (DRS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The XRD and SEM results revealed that the PI exhibited a high degree of polymerization. The DRS characterization showed that the light absorption exhibited regular shifts upon the change of PI/Zn 0.25 Cd 0.75 S mass ratio. The TEM results proved the in situ growth of finely distributed Zn 0.25 Cd 0.75 S nanoparticles on the surface of PI sheets. The as-prepared samples exhibited superior photocatalytic activity compared with PI and Zn 0.25 Cd 0.75 S toward the degradation of dyes under visible light irradiation. The electrochemical impedance spectroscopy (EIS) confirmed that the separation efficiency of electron–hole pairs was greatly improved for the formation of heterojunction. The activity enhancement of PI/Zn 0.25 Cd 0.75 S composites could be attributed to the interfacial electronic interaction and high migration efficiency of photo-induced carriers. A possible photodegradation mechanism was proposed for the degradation of dyes over PI/Zn 0.25 Cd 0.75 S composites

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

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.

Associated chemical and carbon isotopic composition variations in diamonds from Finsch and Premier kimberlite, South Africa

International Nuclear Information System (INIS)

Deines, P.

1984-01-01

The carbon isotopic composition of 66 inclusion-containing diamonds from the Premier kimberlite, South Africa, 93 inclusion-containing diamonds and four diamonds of two diamond-bearing peridotite xenoliths from the Finsch kimberlite, South Africa was measured. The data suggest a relationship between the carbon isotopic composition of the diamonds and the chemical composition of the associated silicates. For both kimberlites similar trends are noted for diamonds containing peridotite-suite inclusions (P-type) and for diamonds containing eclogite-suite inclusions (E-type): Higher delta 13 C P-type diamonds tend to have inclusions lower in SiO 2 , Al 2 O 3 , Cr 2 O 3 , MgO, Mg/(Mg + Fe) and higher in FeO and CaO. Higher delta 13 C E-type diamonds tend to have inclusions lower in SiO 2 , Al 2 O 3 , MgO, Mg/(Mg + Fe), Na 2 O, K 2 O, TiO 2 and higher in CaO, Ca/(Ca + Mg). Consideration of a number of different models that have been proposed for the genesis of kimberlites, their zenoliths and diamonds shows that they are all consistent with the conclusion that in the mantle, regions exist that are characterized by different mean carbon isotopic compositions. (author)

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

Synthesis and highly visible-induced photocatalytic activity of CNT-CdSe composite for methylene blue solution

Directory of Open Access Journals (Sweden)

Chen Ming-Liang

2011-01-01

Full Text Available Abstract Carbon nanotube-cadmium selenide (CNT-CdSe composite was synthesized by a facile hydrothermal method derived from multi-walled carbon nanotubes as a stating material. The as-prepared products were characterized by X-ray diffraction, scanning electron microscopy with energy dispersive X-ray analysis, transmission electron microscopy (TEM, and UV-vis diffuse reflectance spectrophotometer. The as-synthesized CNT-CdSe composite efficiently catalyzed the photodegradation of methylene blue in aqueous solutions under visible-light irradiation, exhibiting higher photocatalytic activity.

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

Ageing and structural effects on the sorption characteristics of Cd2+ by clinoptilolite and Y-type zeolite studied using isotope exchange technique

International Nuclear Information System (INIS)

Ahmed, I.A.M.; Young, S.D.; Crout, N.M.J.

2010-01-01

This research investigates the long-term kinetics of Cd 2+ sorption and desorption by calcium-exchanged clinoptilolite (CaCpt) and Y-type (CaY) zeolite using isotopic exchange with 109 Cd while maintaining pH at circumneutral values. The effects of Si/Al ratio and crystal structure of these zeolitic materials on intracrystalline transport of Cd are discussed. A first-order kinetic model was developed to describe the progressive transfer of Cd 2+ to a less reactive form within the zeolite structure, following initial sorption and subsequent desorption of Cd subject to different initial contact times. The kinetic model differentiates between two forms of sorbed Cd 2+ designated 'labile' and 'non-labile' in which the labile form is in immediate equilibrium with the free Cd 2+ ion activity in solution. A model combining diffusion and first-order kinetics for cation exchange was also employed to determine Cd 2+ diffusivity and intracrystalline exchange rates in CaY and CaCpt. The efficiency of Permeable Reactive Barriers (PRBs) containing zeolitic materials in protecting water systems against lateral flow of metal-contaminated leachate was simulated for three contrasting zeolites. The slow transfer of Cd between labile and non-labile forms was particularly important in moderating high concentration pulses of Cd traversing the PRB. In addition, the reversibility of Cd fixation effectively restored the sorption capability of the zeolite through slow leakage to drainage water.

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

Isomer spectroscopy of {sup 125,127}Cd

Energy Technology Data Exchange (ETDEWEB)

Naqvi, F. [Institut fuer Kernphysik, Universitaet Koeln (Germany); GSI, Helmholtzzentrum fuer Schwerionenforschung, Darmstadt (Germany); Gorska, M.; Grawe, H.; Pietri, S. [GSI, Helmholtzzentrum fuer Schwerionenforschung, Darmstadt (Germany); Caceres, L. [GSI, Helmholtzzentrum fuer Schwerionenforschung, Darmstadt (Germany); Departmento de Fisicia Teorica, Universidad Autonoma de Madrid (Spain); Jungclaus, A. [Departmento de Fisicia Teorica, Universidad Autonoma de Madrid (Spain); Pfuetzner, M. [IEP, Warsaw University, Warsaw (Poland); Regan, P.H; Podolyak, Z. [Department of Physics, University of Surrey, Guildford (United Kingdom); Rudolf, D. [Department of Physics, Lund University (Sweden)

2010-07-01

The results of investigations of isomeric decay in odd mass heavy Cd isotopes namely {sup 125,127}Cd are reported. To date information has been obtained on even mass heavy Cd isotopes and the systematics show evolution of single particle energies for them. The experiment was performed at GSI, Darmstadt to investigate the single particle level structure of odd mass heavy Cd isotopes. Nuclei of interest were produced in fragmentation reaction of {sup 136}Xe beam at energy 750MeV/u on a {sup 9}Be target of 4g/cm{sup 2} thickness. Selection of ions from unwanted reaction products and event by event identification was facilitated by FRagment Separator (FRS). Isomers populated in the reaction were implanted in a plastic catcher surrounded by 15 Ge cluster detectors from RISING array to detect gamma radiations. Level schemes based on the intensity balance and life time information were constructed for the first time for these nuclei. Comparison of the experimental results with shell model calculation are discussed.

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)

Improved photoluminescence quantum yield and stability of CdSe-TOP, CdSe-ODA-TOPO, CdSe/CdS and CdSe/EP nanocomposites

Science.gov (United States)

Wei, Shutian; Zhu, Zhilin; Wang, Zhixiao; Wei, Gugangfen; Wang, Pingjian; Li, Hai; Hua, Zhen; Lin, Zhonghai

2016-07-01

Size-controllable monodisperse CdSe nanocrystals with different organic capping were prepared based on the hot-injection method. The effective separation of nucleation and growth was achieved by rapidly mixing two highly reactive precursors. As a contrast, we prepared CdSe/CdS nanocrystals (NCs) successfully based on the selective ion layer adsorption and reaction (SILAR) technique. This inorganic capping obtained higher photoluminescence quantum yield (PLQY) of 59.3% compared with organic capping of 40.8%. Furthermore, the CdSe-epoxy resin (EP) composites were prepared by adopting a flexible ex situ method, and showed excellent stability in the ambient environment for one year. So the composites with both high PLQY of nanocrystals and excellent stability are very promising to device application.

Methane clumped isotopes: Progress and potential for a new isotopic tracer

Energy Technology Data Exchange (ETDEWEB)

Douglas, Peter M. J.; Stolper, Daniel A.; Eiler, John M.; Sessions, Alex L.; Lawson, Michael; Shuai, Yanhua; Bishop, Andrew; Podlaha, Olaf G.; Ferreira, Alexandre A.; Santos Neto, Eugenio V.; Niemann, Martin; Steen, Arne S.; Huang, Ling; Chimiak, Laura; Valentine, David L.; Fiebig, Jens; Luhmann, Andrew J.; Seyfried, William E.; Etiope, Giuseppe; Schoell, Martin; Inskeep, William P.; Moran, James J.; Kitchen, Nami

2017-11-01

The isotopic composition of methane is of longstanding geochemical interest, with important implications for understanding hydrocarbon systems, atmospheric greenhouse gas concentrations, the global carbon cycle, and life in extreme environments. Recent analytical developments focusing on multiply substituted isotopologues (‘clumped isotopes’) are opening a potentially valuable new window into methane geochemistry. When methane forms in internal isotopic equilibrium, clumped isotopes can provide a direct record of formation temperature, making this property particularly valuable for identifying different methane origins. However, it has also become clear that in certain settings methane clumped isotope measurements record kinetic rather than equilibrium isotope effects. Here we present a substantially expanded dataset of methane clumped isotope analyses, and provide a synthesis of the current interpretive framework for this parameter. We review different processes affecting methane clumped isotope compositions, describe the relationships between conventional isotope and clumped isotope data, and summarize the types of information that this measurement can provide in different Earth and planetary environments.

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

First direct mass measurements of stored neutron-rich 129,130,131Cd isotopes with FRS-ESR

Directory of Open Access Journals (Sweden)

R. Knöbel

2016-03-01

Full Text Available A 410 MeV/u 238U projectile beam was used to create cadmium isotopes via abrasion-fission in a beryllium target placed at the entrance of the in-flight separator FRS at GSI. The fission fragments were separated by the FRS and injected into the isochronous storage ring ESR for mass measurements. Isochronous Mass Spectrometry (IMS was performed under two different experimental conditions, with and without Bρ-tagging at the high-resolution central focal plane of the FRS. In the experiment with Bρ-tagging the magnetic rigidity of the injected fragments was determined with an accuracy of 2⋅10−4. A new method of data analysis, which uses a correlation matrix for the combined data set from both experiments, has provided experimental mass values of 25 rare isotopes for the first time. The high sensitivity and selectivity of the method have given access to nuclides detected with a rate of a few atoms per week. In this letter we present for the 129,130,131Cd isotopes mass values directly measured for the first time. The experimental mass values of cadmium as well as for tellurium and tin isotopes show a pronounced shell effect towards and at N=82. Shell quenching cannot be deduced from a single new mass value, nor by a better agreement with a theoretical model which explicitly takes into account a quenching feature. This is in agreement with the conclusion from γ-ray spectroscopy and confirms modern shell-model calculations.

Introduction to Body Composition Assessment Using the Deuterium Dilution Technique with Analysis of Urine Samples by Isotope Ratio Mass Spectrometry

International Nuclear Information System (INIS)

2010-01-01

The IAEA has fostered the more widespread use of a stable isotope technique to assess body composition in different population groups to address priority areas in public health nutrition in Member States. It has done this by supporting national and regional nutrition projects through its technical cooperation programme and coordinated research projects over many years. This publication was developed by an international group of experts to provide practical hands-on guidance in the use of this technique in settings where analysis of stable isotope ratios in biological samples is to be made by isotope ratio mass spectrometry. The publication is targeted at new users of this technique, for example nutritionists, analytical chemists and other professionals. More detailed information on the theoretical background and the practical applications of state of the art methodologies to monitor changes in body composition can be found in IAEA Human Health Series No. 3, Assessment of Body Composition and Total Energy Expenditure in Humans by Stable Isotope Techniques

Balloon measurement of the isotopic composition of galactic cosmic ray boron, carbon, and nitrogen

International Nuclear Information System (INIS)

Zumberge, J.F.

1981-01-01

The isotopic compositions of galactic cosmic ray boron, carbon, and nitrogen have been measured at energies near 300 MeV amu -1 , using a balloon-borne instrument at an atmospheric depth of approx. 5 g cm -2 . The calibrations of the detectors comprising the instrument are described. The saturation properties of the cesium iodide scintillators used for measurement of particle energy are studied in the context of analyzing the data for mass. The achieved rms mass resolution varies from approx. 0.3 amu at boron to approx. 0.5 amu at nitrogen, consistent with a theoretical analysis of the contributing factors. A model of galactic propagation and solar modulation is described. Assuming a cosmic ray source composition of solar-like isotopic abundances, the model predicts abundances near earth consistent with the measurements

Chemical and isotopic composition of secondary organic aerosol generated by α-pinene ozonolysis

DEFF Research Database (Denmark)

Meusinger, Carl; Dusek, Ulrike; King, Stephanie M.

2017-01-01

-NOx conditions, with OH scavengers and in the absence of seed particles. The excess of ozone and long residence time in the flow chamber ensured that virtually all α-pinene had reacted. Product SOA was collected on two sequential quartz filters. The filters were analysed offline by heating them stepwise from 100...... it is difficult to apply because neither the isotopic composition of aerosol precursors nor the fractionation of aerosol forming processes is well characterised. In this paper, SOA formation from ozonolysis of α-pinene - an important precursor and perhaps the best-known model system used in laboratory studies...... - was investigated using position-dependent and average determinations of 13C in α-pinene and advanced analysis of reaction products using thermal-desorption proton-transfer-reaction mass spectrometry (PTR-MS). The total carbon (TC) isotopic composition δ13C of the initial α-pinene was measured, and the δ13C...

Heavy metals pollution and pb isotopic signatures in surface sediments collected from Bohai Bay, North China.

Science.gov (United States)

Gao, Bo; Lu, Jin; Hao, Hong; Yin, Shuhua; Yu, Xiao; Wang, Qiwen; Sun, Ke

2014-01-01

To investigate the characteristics and potential sources of heavy metals pollution, surface sediments collected from Bohai Bay, North China, were analyzed for the selected metals (Cd, Cr, Cu, Ni, Pb, and Zn). The Geoaccumulation Index was used to assess the level of heavy metal pollution. Pb isotopic compositions in sediments were also measured to effectively identify the potential Pb sources. The results showed that the average concentrations of Cd, Cr, Cu, Ni, Pb, and Zn were 0.15, 79.73, 28.70, 36.56, 25.63, and 72.83 mg/kg, respectively. The mean concentrations of the studied metals were slightly higher than the background values. However, the heavy metals concentrations in surface sediments in Bohai Bay were below the other important bays or estuaries in China. The assessment by Geoaccumulation Index indicated that Cr, Zn, and Cd were classified as "the unpolluted" level, while Ni, Cu, and Pb were ranked as "unpolluted to moderately polluted" level. The order of pollution level of heavy metals was: Pb > Ni > Cu > Cr > Zn > Cd. The Pb isotopic ratios in surface sediments varied from 1.159 to 1.185 for (206)Pb/(207)Pb and from 2.456 to 2.482 for (208)Pb/(207)Pb. Compared with Pb isotopic radios in other sources, Pb contaminations in the surface sediments of Bohai Bay may be controlled by the mix process of coal combustion, aerosol particles deposition, and natural sources.

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)

Mixed Cd-Zn sulfides / Pt-TiO2 composites : bottlenecks limiting efficiency of photocatalytic water reduction

NARCIS (Netherlands)

Litke, A.; Weber, Th.; Hofmann, J.P.; Hensen, E.J.M.

2016-01-01

Visible-light driven photocatalytic water reduction on composite materials consisting of platinized titania (Pt-TiO2) and transition metal sulfides (CdS or Cd0.5Zn0.5S) was investigated in detail. Sulfides were prepared by hydrothermal synthesis and room-temperature precipitation. The parameters

A discussion for the evolution model of Pb isotope of the upper mantle in western Yunnan and its interpretation to the lead isotopic compositions of the regional alkali-rich porphyries and their related rocks

International Nuclear Information System (INIS)

Wu Kaixing; Hu Ruizhong; Bi Xianwu; Zhang Qian; Peng Jiantang

2003-01-01

Thirty Pb isotope data of the upper mantle in the area of western Yunnan have the similar trends with the Stacey-Kramers' two stage model growth curves but apparently deviate from it on the lead isotope composition programs, which may suggest Pb isotope of the upper mantle in the area of western Yunnan might have two stage evolution history though not fit very well to the Stacey-Kramers' two stage model growth curves. In this paper, a two-stage growth curves which can better fit the Pb isotope data was constructed based on the lead isotope data of the upper mantle in western Yunnan and the principle that Stacey and Kramers constructed the two-stage model and a reasonable interpretation was given to the lead isotopic compositions of the regional alkali-rich porphyries and their related rocks using the model. (authors)

The O and H stable isotope composition of freshwaters in the British Isles. 2. Surface waters and groundwater

Directory of Open Access Journals (Sweden)

W. G. Darling

2003-01-01

Full Text Available The utility of stable isotopes as tracers of the water molecule has a long pedigree. The study reported here is part of an attempt to establish a comprehensive isotopic 'baseline' for the British Isles as background data for a range of applications. Part 1 of this study (Darling and Talbot, 2003 considered the isotopic composition of rainfall in Britain and Ireland. The present paper is concerned with the composition of surface waters and groundwater. In isotopic terms, surface waters (other than some upland streams are poorly characterised in the British Isles; their potential variability has yet to be widely used as an aid in hydrological research. In what may be the first study of a major British river, a monthly isotopic record of the upper River Thames during 1998 was obtained. This shows high damping of the isotopic variation compared to that in rainfall over most of the year, though significant fluctuations were seen for the autumn months. Smaller rivers such as the Stour and Darent show a more subdued response to the balance between runoff and baseflow. The relationship between the isotopic composition of rainfall and groundwater is also considered. From a limited database, it appears that whereas Chalk groundwater is a representative mixture of weighted average annual rainfall, for Triassic sandstone groundwater there is a seasonal selection of rainfall biased towards isotopically-depleted winter recharge. This may be primarily the result of physical differences between the infiltration characteristics of rock types, though other factors (vegetation, glacial history could be involved. In the main, however, groundwaters appear to be representative of bulk rainfall within an error band of 0.5‰ δ18O. Contour maps of the δ18O and δ2H content of recent groundwaters in the British Isles show a fundamental SW-NE depletion effect modified by topography. The range of measured values, while much smaller than those for rainfall, still covers

Single-particle states in ^112Cd probed with the ^111Cd(d,p) reaction

Science.gov (United States)

Garrett, P. E.; Jamieson, D.; Demand, G. A.; Finlay, P.; Green, K. L.; Leach, K. G.; Phillips, A. A.; Sumithrarachchi, C. S.; Svensson, C. E.; Triambak, S.; Wong, J.; Ball, G. C.; Hertenberger, R.; Wirth, H.-F.; Kr"Ucken, R.; Faestermann, T.

2009-10-01

As part of a program of detailed spectroscopy of the Cd isotopes, the single-particle neutron states in ^112Cd have been probed with the ^111Cd(d,p) reaction. Beams of polarized 22 MeV deuterons, obtained from the LMU/TUM Tandem Accelerator, bombarded a target of ^111Cd. The protons from the reaction, corresponding to excitation energies up to 3 MeV in ^112Cd, were momentum analyzed with the Q3D spectrograph. Cross sections and analyzing powers were fit to results of DWBA calculations, and spectroscopic factors were determined. The results from the experiment, and implications for the structure of ^112Cd, will be presented.

Effects of different water storage procedures on the dissolved Fe concentration and isotopic composition of chemically contrasted waters from the Amazon River Basin.

Science.gov (United States)

Mulholland, Daniel S; Poitrasson, Franck; Boaventura, Geraldo R

2015-11-15

Although recent studies have investigated the Fe isotopic composition of dissolved, colloidal and particulate phases from continental and oceanic natural waters, few efforts have been made to evaluate whether water sample storage and the separation of different pore-size fractions through filtration can cause any change to the Fe isotopic compositions. The present study investigates the possible biases introduced by different water storage conditions on the dissolved Fe concentration and isotopic composition of chemically different waters. Water samples were collected from an organic-rich river and from mineral particulate-rich rivers. Filtered and unfiltered water samples were stored either at room temperature or frozen at -18°C in order to assess possible biases due to (i) different water storage temperature, and (ii) storage of bulk (unfiltered) vs filtered water. Iron isotope measurements were performed by Multicollector Inductively Coupled Plasma Mass Spectrometry with a Thermo Electron Neptune instrument, after Fe purification using anion-exchange resins. Our data reveal that bulk water storage at room temperature without filtration produces minor changes in the dissolved Fe isotopic composition of mineral particulate-rich waters, but significant isotopic composition changes in organic-rich waters. In both cases, however, the impact of the different procedures on the Fe concentrations was strong. On the other hand, the bulk water stored frozen without filtration produced more limited changes in the dissolved Fe concentrations, and also on isotopic compositions, relative to the samples filtered in the field. The largest effect was again observed for the organic-rich waters. These findings suggest that a time lag between water collection and filtration may cause isotopic exchanges between the dissolved and particulate Fe fractions. When it is not possible to filter the samples in the field immediately after collection, the less detrimental approach is to

Investigation of dosimetric characteristics of a core-shell quantum dots nano composite (CdTe/CdS/PMMA): fabrication of a new gamma sensor

Science.gov (United States)

Feizi, Shahzad; Zare, Hakimeh; Hoseinpour, Masoumeh

2018-06-01

CdTe/CdS-PMMA nanocomposite was prepared using dispersion of CdTe/CdS core-shell quantum dots (QDs) in poly methyl methacrylate (PMMA) polymer matrix. High-quality CdTe/CdS core/shell quantum dots were synthesized in aqueous solution and were transferred from water to chloroform using ligand-exchange process in the presence of 1-dodecanethiol (1-DDT). Transmission electron microscopy analysis reveals that the obtained nano-particles are highly crystalline nature with mean diameter of 3.6 nm. To prepare an ohmic contact detector, a conductive cell with two silver coated walls was designed and fabricated for exploring gamma detecting properties of the nano composite. New detector was assessed for the linearity of doserate response, angular dependence, sensitivity and repeatability. The results show that the dose rate response of the prepared sensor is linear in the dose rate range of 50-145 mGy/min. So this nanocomposite can be utilized as a potential gamma sensor in the medical radiation device design.

The effect of environmental factors on stable isotopic composition of n-alkanes in Mediterranean olive oils

Science.gov (United States)

Pedentchouk, Nikolai; Mihailova, Alina; Abbado, Dimitri

2014-05-01

Traceability of the geographic origin of olive oils is an important issue from both commercial and health perspectives. This study evaluates the impact of environmental factors on stable C and H isotope compositions of n-alkanes in extra virgin olive oils from Croatia, France, Greece, Italy, Morocco, Portugal, Slovenia, and Spain. The data are used to investigate the applicability of stable isotope methodology for olive oil regional classification in the Mediterranean region. Analysis of stable C isotope composition of n-C29 alkane showed that extra virgin olive oils from Portugal and Spain have the most positive n-C29 alkane delta13C values. Conversely, olive oils from Slovenia, northern and central Italy are characterized by the most negative values. Overall, the n-C29 alkane delta13C values show a positive correlation with the mean air temperature during August-December and a negative correlation with the mean relative humidity during these months. Analysis of stable H isotope composition of n-C29 alkane revealed that the deltaD values are the most positive in olive oils from Greece and Morocco and the most negative in oils from northern Italy. The deltaD values of oils show significant correlation with all the analyses geographical parameters: the mean air temperature and relative humidity during August-December, the total amount of rainfall (the same months) and the annual deltaD values of precipitation. As predictor variables in the Categorical Data Analysis, the n-C29 alkane deltaD values show the most significant discriminative power, followed by the n-C29 alkane delta13C values. Overall, 93.4% of olive oil samples have been classified correctly into one of the production regions. Our findings suggest that an integrated analysis of C and H isotope compositions of n-alkanes extracted from extra virgin olive oil could become a useful tool for geographical provenancing of this highly popular food commodity.

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)

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

Determination of lead isotopic composition of airborne particulate matter by ICPMS: implications for lead atmospheric emissions in Canada

International Nuclear Information System (INIS)

Celo, V.; Dabek-Zlotorzynska, E.

2009-01-01

Full text: Quadrupole ICPMS was used for determination of trace metal concentrations and lead isotopic composition in fine particulate matter (PM 2.5 ) collected at selected sites within the Canadian National Air Pollution Surveillance network, from February 2005 to February 2007. High enrichment factors indicated that lead is mostly of anthropogenic origin and consequently, the lead isotopic composition is directly related to that of pollution sources. The 206 Pb/ 207 Pb and 208 Pb/ 207 Pb ratios were measured and the results were compared to the isotopic signatures of lead from different sources. Various approaches were used to assess the impact of relevant sources and the meteorological conditions in the occurrence and distribution of lead in Canadian atmospheric aerosols. (author)

Temporal variations of methane concentration and isotopic composition in groundwater of the St. Lawrence Lowlands, eastern Canada

Science.gov (United States)

Rivard, Christine; Bordeleau, Geneviève; Lavoie, Denis; Lefebvre, René; Malet, Xavier

2018-03-01

Dissolved methane concentrations in shallow groundwater are known to vary both spatially and temporally. The extent of these variations is poorly documented although this knowledge is critical for distinguishing natural fluctuations from anthropogenic impacts stemming from oil and gas activities. This issue was addressed as part of a groundwater research project aiming to assess the risk of shale gas development for groundwater quality over a 500-km2 area in the St. Lawrence Lowlands (Quebec, Canada). A specific study was carried out to define the natural variability of methane concentrations and carbon and hydrogen isotope ratios in groundwater, as dissolved methane is naturally ubiquitous in aquifers of this area. Monitoring was carried out over a period of up to 2.5 years in seven monitoring wells. Results showed that for a given well, using the same sampling depth and technique, methane concentrations can vary over time from 2.5 to 6 times relative to the lowest recorded value. Methane isotopic composition, which is a useful tool to distinguish gas origin, was found to be stable for most wells, but varied significantly over time in the two wells where methane concentrations are the lowest. The use of concentration ratios, as well as isotopic composition of methane and dissolved inorganic carbon (DIC), helped unravel the processes responsible for these variations. This study indicates that both methane concentrations and isotopic composition, as well as DIC isotopes, should be regularly monitored over at least 1 year to establish their potential natural variations prior to hydrocarbon development.

Sulfur Isotope Composition of Some Polymetallic Deposits in the Republic of Macedonia

International Nuclear Information System (INIS)

Serafimovski, Todor; Tasev, Goran

2005-01-01

The attempt to obtain an exact information about the origin of sulfur and other metals present in polymetallic deposits at the territory of the Republic of Macedonia have resulted in a detailed sulfur isotope composition study, which have enclosed the following deposits: Toranica, Sasa, Zletovo, Buchim and Alshar deposit. Results obtained for the formerly mentioned deposits have shown that sulfur isotope composition β 34 S is in the range -7.52 to +2.18 per mils in Toranica, -1.22 -- +6.94 per mils in Sasa, -3.12 -- +3.40 per mils in Zletovo (without ore associated barites), +0.00 to +2.53 per mils in Buchim (the narrowest range of all studied deposits) and -6.84 to +0.351 per mils β 34 S in Alshar. Therefore, the most probably origin of primary sulfur in studied deposits from Earth's crust or eventually Upper Mantle. Such sources of sulfur and other mineralizing metals confirmed the theories about the endo gene origin of mineralization fluids, which have formed studied deposits. (Author)

The impact of moisture sources on the oxygen isotope composition of precipitation at a continental site in central Europe

Science.gov (United States)

Krklec, Kristina; Domínguez-Villar, David; Lojen, Sonja

2018-06-01

The stable isotope composition of precipitation records processes taking place within the hydrological cycle. Potentially, moisture sources are important controls on the stable isotope composition of precipitation, but studies focused on this topic are still scarce. We studied the moisture sources contributing to precipitation at Postojna (Slovenia) from 2009 to 2013. Back trajectory analyses were computed for the days with precipitation at Postojna. The moisture uptake locations were identified along these trajectories using standard hydrometeorological formulation. The moisture uptake locations were integrated in eight source regions to facilitate its comparison to the monthly oxygen isotope composition (δ18O values) of precipitation. Nearly half of the precipitation originated from continental sources (recycled moisture), and >40% was from central and western Mediterranean. Results show that moisture sources do not have a significant impact on the oxygen isotope composition at this site. We suggest that the large proportion of recycled moisture originated from transpiration rather than evaporation, which produced water vapour with less negative δ18O values. Thus the difference between the oceanic and local vapour source was reduced, which prevented the distinction of the moisture sources based on their oxygen isotope signature. Nevertheless, δ18O values of precipitation are partially controlled by climate parameters, which is of major importance for paleoclimate studies. We found that the main climate control on Postojna δ18O values of precipitation is the surface temperature. Amount effect was not recorded at this site, and the winter North Atlantic Oscillation (NAO) does not impact the δ18O values of precipitation. The Western Mediterranean Oscillation (WeMO) was correlated to oxygen stable isotope composition, although this atmospheric pattern was not a control. Instead we found that the link to δ18O values results from synoptic scenarios affecting We

The evaporation pan technique revisited: Old theory and a new application for time-weighted synoptic tracing of the isotopic composition of atmospheric vapour

International Nuclear Information System (INIS)

Gibson, J.J.; Edwards, T.W.D.

1999-01-01

Reliable and consistent characterization of the stable isotope composition of atmospheric water vapour and its temporal variability are important prerequisites to the wider application of isotope mass balance methods in atmospheric and water balance studies. A new approach is proposed which utilizes standard class-A evaporation pans, which have sufficient volume to buffer short-term transient variations in atmospheric conditions, justifying the assumption of constant kinetic isotopic fractionation effects in concert with precisely measured temperature and relative humidity to derive vapour isotopic composition. The results of the studies suggest that isotopic sampling of existing, conventionally operated class-A evaporation pans could offer a straightforward and cost-effective solution to the problem of documenting the shifting isotopic distribution in atmospheric moisture

Environmental isotopes, chemical composition and groundwater recharge in ataqa-north galala region, Egypt

International Nuclear Information System (INIS)

Shohaib, R.EL-SH.; Nada, A.; Safie El-Din, A.

1991-01-01

Groundwater samples collected from a number of localities in ataqa-north galala region were subjected to various chemical and isotopic analyses. The seasonal fluctuations in hydrochemical composition reveal that the marin Mg Cl 2 type is dominant in the aquifer through-out the year. The Ca Cl 2 water type of marine origin appears in January in wells W 3 and W 7 which lie close to sukhna fault. Recharge to the aquifer is reflected by fluctuation in the water level and fluctuations of the hydrochemical composition of the water. The results of the isotopic content of the water samples indicate that the connate marine water has been subjected to dilution and mixing by the meteoric water invasion since the pliestocene pluvial period (paleowater) and recent meteoric water precipitation. The bulk of the stored water ( about 80%) is paleowater and the recent water (20%) are percolate ones derived from the rain-fall at high latitudes.4 fig. 1 tab

Stable water isotope patterns in a climate change hotspot: the isotope hydrology framework of Corsica (western Mediterranean).

Science.gov (United States)

van Geldern, Robert; Kuhlemann, Joachim; Schiebel, Ralf; Taubald, Heinrich; Barth, Johannes A C

2014-06-01

The Mediterranean is regarded as a region of intense climate change. To better understand future climate change, this area has been the target of several palaeoclimate studies which also studied stable isotope proxies that are directly linked to the stable isotope composition of water, such as tree rings, tooth enamel or speleothems. For such work, it is also essential to establish an isotope hydrology framework of the region of interest. Surface waters from streams and lakes as well as groundwater from springs on the island of Corsica were sampled between 2003 and 2009 for their oxygen and hydrogen isotope compositions. Isotope values from lake waters were enriched in heavier isotopes and define a local evaporation line (LEL). On the other hand, stream and spring waters reflect the isotope composition of local precipitation in the catchment. The intersection of the LEL and the linear fit of the spring and stream waters reflect the mean isotope composition of the annual precipitation (δP) with values of-8.6(± 0.2) ‰ for δ(18)O and-58(± 2) ‰ for δ(2)H. This value is also a good indicator of the average isotope composition of the local groundwater in the island. Surface water samples reflect the altitude isotope effect with a value of-0.17(± 0.02) ‰ per 100 m elevation for oxygen isotopes. At Vizzavona Pass in central Corsica, water samples from two catchments within a lateral distance of only a few hundred metres showed unexpected but systematic differences in their stable isotope composition. At this specific location, the direction of exposure seems to be an important factor. The differences were likely caused by isotopic enrichment during recharge in warm weather conditions in south-exposed valley flanks compared to the opposite, north-exposed valley flanks.

Isotopic composition of reduced and oxidized sulfur in the Canary Islands: implications for the mantle S cycle

Science.gov (United States)

Beaudry, P.; Longpre, M. A.; Wing, B. A.; Bui, T. H.; Stix, J.

2017-12-01

The Earth's mantle contains distinct sulfur reservoirs, which can be probed by sulfur isotope analyses of volcanic rocks and gases. We analyzed the isotopic composition of reduced and oxidized sulfur in a diverse range of volcanically derived materials spanning historical volcanism in the Canary Islands. Our sample set consists of subaerial volcanic tephras from three different islands, mantle and sedimentary xenoliths, as well as lava balloon samples from the 2011-2012 submarine El Hierro eruption and associated crystal separates. This large sample set allows us to differentiate between the various processes responsible for sulfur isotope heterogeneity in the Canary archipelago. Our results define an array in triple S isotope space between the compositions of the MORB and seawater sulfate reservoirs. Specifically, the sulfide values are remarkably homogeneous around d34S = -1 ‰ and D33S = -0.01 ‰, while sulfate values peak at d34S = +4 ‰ and D33S = +0.01 ‰. Lava balloons from the El Hierro eruption have highly enriched sulfate d34S values up to +19.3 ‰, reflecting direct interaction between seawater sulfate and the erupting magma. Several sulfate data points from the island of Lanzarote also trend towards more positive d34S up to +13.8 ‰, suggesting interaction with seawater sulfate-enriched lithologies or infiltration of seawater within the magmatic system. On the other hand, the modal values and relative abundances of S2- and S6+ in crystal separates suggest that the Canary Island mantle source has a d34S around +3 ‰, similar to the S-isotopic composition of a peridotite xenolith from Lanzarote. We infer that the S2- and S6+ modes reflect isotopic equilibrium between those species in the magmatic source, which requires 80 % of the sulfide to become oxidized after melting, consistent with measured S speciation. This 34S enrichment of the source could be due to the recycling of hydrothermally-altered oceanic crust, which has been previously suggested

Isotopic composition and radiological properties of uranium in selected fuel cycles

International Nuclear Information System (INIS)

Fleischman, R.M.; Liikala, R.C.

1975-04-01

Three major topic areas are discussed: First, the properties of the uranium isotopes are defined relative to their respective roles in the nuclear fuel cycle. Secondly, the most predominant fuel cycles expected in the U. S. are described. These are the Light Water Reactor (LWR), High Temperature Gas Cooled Reactor (HTGR), and Liquid Metal Fast Breeder Reactor (LMFBR) fuel cycles. The isotopic compositions of uranium and plutonium fuels expected for these fuel cycles are given in some detail. Finally the various waste streams from these fuel cycles are discussed in terms of their relative toxicity. Emphasis is given to the high level waste streams from reprocessing of spent fuel. Wastes from the various fuel cycles are compared based on projected growth patterns for nuclear power and its various components. (U.S.)

18O, 2H and 3H isotopic composition of precipitation and shallow groundwater in Olkiluoto

International Nuclear Information System (INIS)

Hendriksson, N.; Karhu, J.; Niinikoski, P.

2014-12-01

The isotopic composition of oxygen and hydrogen in local precipitation is a key parameter in the modelling of local water circulation. This study was initiated in order to provide systematic monthly records of the isotope content of atmospheric precipitation in the Olkiluoto area and to establish the relation between local rainfall and newly formed groundwater. During January 2005 - December 2012, a total of 85 cumulative monthly rainfall samples and 68 shallow groundwater samples were collected and the isotopic composition of oxygen and hydrogen was recorded for all those samples. Tritium values are available for 79 precipitation and 65 groundwater samples. Based on the 8-year monitoring, the long-term weighted annual mean isotope values of precipitation and the mean values of shallow groundwater are -11.59 per mille and -11.27 per mille for δ 18 O, - 82.3 per mille and -80.3 per mille for δ 2 H and 9.8 and 9.1 TU for tritium, respectively. Based on these data, the mean stable isotope ratios of groundwater represent the long-term mean annual isotopic composition of local precipitation. The precipitation data were used to establish the local meteoric water line (LMWL) for the Olkiluoto area. The line is formulated as: δ 2 H = 7.45 star δ 18 O + 3.82. The isotope time series reveal a change in time. The increasing trend for the δ 18 O and δ 2 H values may be related to climatic variability while the gradual decline observed in the 3 H data is attributed to the still continuing decrease in atmospheric 3 H activity in the northern hemisphere. The systematic seasonal and long-term tritium trends suggest that any potential ground-level tritium release from the Olkiluoto nuclear power plants is insignificant. The d-excess values of Olkiluoto precipitation during the summer period indicated that a notable amount of re-cycled Baltic Sea water may have contributed to precipitation in the Finnish southern coast. Preliminary estimates of the evaporated Baltic Sea water

The Investigation of Isotopic Composition of Precipitation and water vapour by Using Air Mass Trajectories and Meteorological Parameters

International Nuclear Information System (INIS)

Dirican, A.; Acar, Y.; Demircan, M.

2002-01-01

In last century there are so many studies were carried out about stable isotopes of precipitation. The Researchers, study in this field directed to examine origin and transport of water vapour. To investigate the conditions of precipitation formation parallel with climatic changes, stable isotopes using as a powerful tool. So that a project coordinated by IAEA. In this presentation we will give some parts of this project which was carried out in Turkey. First results were obtained for 2001 year. The one of the first result which was obtained in this project is the relation between air temperature and isotopic composition of precipitation collected in Ankara Antalya and Adana station. Second was the observation of temporal variation of stable isotope composition in precipitation and water vapour in relation with water vapour transport. δD and δ 18 O content of atmospheric water vapour examined for January - December 2001 time interval. 27 precipitation event had been examined, starting from endengered place and following to trajectories until to reach Turkey, by using ground level and 500mbar synoptic charts. The observed δD and δ 18 O variations of water vapour is related with the endengered place (Atlantic Ocean, Mediterranean Sea, etc.) of water vapour. The isotopic composition of local precipitation forms by regional meteorological factors. In this study δD and δ 18 O relation of event, daily precipitation and water vapour were defined

A new method of accurate determination of isotopic composition and concentration of strontium in a spike solution used for geochronological works

International Nuclear Information System (INIS)

Yanagi, Takeru

1990-01-01

A new method of accurate determination of isotopic composition and concentration of a strontium-84 spike solution was devised for simultaneous determination of strontium contents and isotopic compositions in rocks and minerals by measuring strontium isotopic ratios in spiked samples. In this method, the isotopic composition of strontium in the spike were determined so as to minimize the sum of squares of deviations of spike strontium-84 concentrations which were calculated from measured isotopic ratios of strontium in five different mixtures of the spike and the standard solution. The method can eliminate all mass discriminations occurred during the measurements on a surface ionization mass spectrometer. The results were tested by measuring 87 Sr/ 86 Sr ratios of Eimer and Amend SrCO 3 and JB-1 geochemical reference material, and by determining the strontium content in JB-1. The measurements of strontium isotope ratios in spiked samples give average values of 0.708007±0.000052 and 0.70417±0.00004 for 87 Sr/ 86 Sr ratios of E and A SrCO 3 and JB-1, respectively. The strontium content in JB-1 was estimated at 457.1±1.3 ppm. These values are very close to reported respective values. (author)

Search for first 0 excited states in /sup 108/Cd and /sup 106/Cd

CERN Document Server

Roussière, B; Duffait, R; Genevey-Rivier, J; Kilcher, P; Meyer, M; Sauvage-Letessier, J; Tréherne, J

1981-01-01

The /sup 108/Cd and /sup 106/Cd isotopes have been studied from the beta /sup +//EC decay of /sup 108/In and /sup 106/In. gamma -rays, conversion electrons, gamma - gamma -t and e/sup -/- gamma -t coincidence measurements have been performed. Level schemes of /sup 108/Cd and /sup 106/Cd have been deduced from these results. A 0/sup + / level has been unambiguously established at 1.913 MeV in /sup 108/Cd and a new 0/sup +/ level proposed at 2.035 MeV in /sup 106/Cd. The energies and branching ratios are discussed in terms of vibrator +particles approach, interacting boson approximation and rotor +quasiparticles model. (15 refs).

Three New Offset {delta}{sup 11}B Isotope Reference Materials for Environmental Boron Isotope Studies

Energy Technology Data Exchange (ETDEWEB)

Rosner, M. [BAM Federal Institute for Materials Research and Testing, Berlin (Germany); IsoAnalysis UG, Berlin (Germany); Vogl, J. [BAM Federal Institute for Materials Research and Testing, Berlin (Germany)

2013-07-15

The isotopic composition of boron is a well established tool in various areas of science and industry. Boron isotope compositions are typically reported as {delta}{sup 11}B values which indicate the isotopic difference of a sample relative to the isotope reference material NIST SRM 951. A significant drawback of all of the available boron isotope reference materials is that none of them covers a natural boron isotope composition apart from NIST SRM 951. To fill this gap of required {delta}{sup 11}B reference materials three new solution boric acid reference materials were produced, which cover 60 per mille of the natural boron isotope variation (-20 to 40 per mille {delta}{sup 11}B) of about 100 per mille . The new reference materials are certified for their {delta}{sup 11}B values and are commercially available through European Reference Materials (http://www.erm-crm.org). The newly produced and certified boron isotope reference materials will allow straightforward method validation and quality control of boron isotope data. (author)

French days on stable isotopes

International Nuclear Information System (INIS)

2000-01-01

These first French days on stable isotopes took place in parallel with the 1. French days of environmental chemistry. Both conferences had common plenary sessions. The conference covers all aspects of the use of stable isotopes in the following domains: medicine, biology, environment, tracer techniques, agronomy, food industry, geology, petroleum geochemistry, cosmo-geochemistry, archaeology, bio-geochemistry, hydrology, climatology, nuclear and particle physics, astrophysics, isotope separations etc.. Abstracts available on CD-Rom only. (J.S.)

Electro-optical and dielectric properties of CdSe quantum dots and 6CHBT liquid crystals composites

Energy Technology Data Exchange (ETDEWEB)

Singh, U. B.; Pandey, M. B., E-mail: mbpandey@gmail.com [Department of Physics, Vikramajit Singh Sanatan Dharama College, Kanpur-208002 (India); Dhar, R; Pandey, A. S. [Centre of Material Sciences, Institute of Interdisciplinary Studies, University of Allahabad, Allahabad-211002 (India); Kumar, S. [Raman Research Institute, C. V. Raman Avenue, Bangalore-560080 (India); Dabrowski, R. [Institute of Applied Sciences and Chemistry, Military University of Technology, 00-908-Warswa (Poland)

2014-11-15

We have prepared the composites of a room temperature nematic liquid crystal namely 4-(trans-4-n-hexylcyclohexyl) isothiocyanatobenzoate (6CHBT) and Cadmium Selenide Quantum Dots (CdSe-QDs) and investigated their electro-optical and dielectric properties. Effect of dispersion of CdSe-QDs on various electro-optical and display parameters of host liquid crystalline material have been studied. Physical parameters, such as switching threshold voltage and splay elastic constant have been altered drastically for composites. Dispersion of QDs in a liquid crystals medium destabilizes nematic ordering of the host and decreases the nematic-to-isotropic transition temperature.

Electro-optical and dielectric properties of CdSe quantum dots and 6CHBT liquid crystals composites

International Nuclear Information System (INIS)

Singh, U. B.; Pandey, M. B.; Dhar, R; Pandey, A. S.; Kumar, S.; Dabrowski, R.

2014-01-01

We have prepared the composites of a room temperature nematic liquid crystal namely 4-(trans-4-n-hexylcyclohexyl) isothiocyanatobenzoate (6CHBT) and Cadmium Selenide Quantum Dots (CdSe-QDs) and investigated their electro-optical and dielectric properties. Effect of dispersion of CdSe-QDs on various electro-optical and display parameters of host liquid crystalline material have been studied. Physical parameters, such as switching threshold voltage and splay elastic constant have been altered drastically for composites. Dispersion of QDs in a liquid crystals medium destabilizes nematic ordering of the host and decreases the nematic-to-isotropic transition temperature

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.

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.

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

Controlling Factors of the Stable Isotope Composition in the Precipitation of Islamabad, Pakistan

Directory of Open Access Journals (Sweden)

Shakir Hussain

2015-01-01

Full Text Available Significant temporal variations in δ18O and deuterium isotopes were found in the rainfall water of Islamabad, Pakistan, over a 15-year period (1992–2006. The data were obtained from the International Atomic Energy Agency/Global Network of Isotopes in Precipitation (IAEA/GNIP database, and statistical correlations were investigated. In particular, this study provides the first detailed analysis of GNIP data for Islamabad. Both dry (1999-2000 and wet years (1994, 1997, and 2000 were chosen to investigate the correlations between precipitation amount, vapor flux, and temperature. We observed obvious differences between the dry and wet years and among seasons as well. Long-term features in the isotope composition agreed with the global meteorological water line, whereas short-term values followed rainfall amounts; that is, a total of 72% of the precipitation’s isotopic signature was dependent on the rainfall amount, and temperature controlled 73% of the isotopic features during October to May. The lower d-excess values were attributed to conditions during the spring season and a secondary evaporation boost during dry years; precipitation originating from the Mediterranean Sea showed high d-excess values. Overall, the results of this study contribute to the understanding of precipitation variations and their association with water vapor transport over Islamabad, Pakistan.

Determination of Cd, Pb, Zn and Cu in Sediment Compartments by Sequential Extraction and Isotope Dilution Inductively Coupled Plasma Mass Spectrometry (ID-ICP-MS

Directory of Open Access Journals (Sweden)

Gardolinski Paulo C. F. C.

2002-01-01

Full Text Available Trace concentrations of Cd, Cu, Pb and Zn in four different sediment fractions extracted in sequence were determined by isotope dilution inductively coupled mass spectrometry (IDICPMS. The metals from each fraction were extracted following the sequential extraction procedure recommended by the Bureau Commun de Référence (BCR of the Commission of the European Communities. As an alternative to external calibration, the elements were quantified by spiking the extracted solutions with 112Cd, 63Cu, 208Pb and 66Zn and application of isotope dilution. The proposed approach was applied to a sample collected from a lake and two standard reference materials, NIST2704 river sediment from the National Institute of Standards & Technology and the BCR-277 estuarine sediment. Detection limits, for each extracted solution, varied from 0.31 to 0.53 mug L¹ for Cd, 0.92 to 2.9 mug L¹ for Cu, 0.22 to 1.1 mug L¹ for Pb and 1.3 to 7.6 mug L¹ for Zn. The sum of the metals concentration in the different fractions was compatible with 95% confidence level found amounts obtained with complete digestion of the samples and with the certified values of the standard reference materials.

Uranium isotopic compositions of the crust and ocean: Age corrections, U budget and global extent of modern anoxia

Science.gov (United States)

Tissot, François L. H.; Dauphas, Nicolas

2015-10-01

The 238U/235U isotopic composition of uranium in seawater can provide important insights into the modern U budget of the oceans. Using the double spike technique and a new data reduction method, we analyzed an array of seawater samples and 41 geostandards covering a broad range of geological settings relevant to low and high temperature geochemistry. Analyses of 18 seawater samples from geographically diverse sites from the Atlantic and Pacific oceans, Mediterranean Sea, Gulf of Mexico, Persian Gulf, and English Channel, together with literature data (n = 17), yield a δ238U value for modern seawater of -0.392 ± 0.005‰ relative to CRM-112a. Measurements of the uranium isotopic compositions of river water, lake water, evaporites, modern coral, shales, and various igneous rocks (n = 64), together with compilations of literature data (n = 380), allow us to estimate the uranium isotopic compositions of the various reservoirs involved in the modern oceanic uranium budget, as well as the fractionation factors associated with U incorporation into those reservoirs. Because the incorporation of U into anoxic/euxinic sediments is accompanied by large isotopic fractionation (ΔAnoxic/Euxinic-SW = +0.6‰), the size of the anoxic/euxinic sink strongly influences the δ238U value of seawater. Keeping all other fluxes constant, the flux of uranium in the anoxic/euxinic sink is constrained to be 7.0 ± 3.1 Mmol/yr (or 14 ± 3% of the total flux out of the ocean). This translates into an areal extent of anoxia into the modern ocean of 0.21 ± 0.09% of the total seafloor. This agrees with independent estimates and rules out a recent uranium budget estimate by Henderson and Anderson (2003). Using the mass fractions and isotopic compositions of various rock types in Earth's crust, we further calculate an average δ238U isotopic composition for the continental crust of -0.29 ± 0.03‰ corresponding to a 238U/235U isotopic ratio of 137.797 ± 0.005. We discuss the implications of

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

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.

Search of the first excited states 0+ of 108Cd and106Cd

International Nuclear Information System (INIS)

Roussiere, B.

1981-01-01

108 Cd and 106 Cd nuclei have been studied from the β + /EC decay of 108 In and 106 In using the isocele II isotope separator working on-line with the Orsay synchrocyclotron. In order to produce indium nuclei, a molten tin target is irradiated by protons (E = 200 MeV) or 3 He (E = 270 MeV). The comparison of saturation activity measured after mass separation with the one measured before mass-separation has allowed us to determine the average delay-time of indium isotopes and the overall efficiency of the separator. Single γ rays, conversion electrons rays, γ-γ-t and γ-e - -t coincidence measurements have been performed to build level schemes of 108 Cd and 106 Cd. In 108 Cd, the first excited 0 + state has been established unambiguously. This state preferably decays to the 2 2 + and not to the 2 1 + as it does in the even-even neighbouring Cd nuclei. An excited 0 + state is proposed in 106 Cd. These states could not be interpreted as headstate of collective band corresponding to a shape different from the ground state one. On the other hand, the model of G. Alaga (vibrator + two proton holes), as well as the IBA2 F. Iachello one seem to be able to describe the low-lying states properties. Finally, the feeding balance and the deduced log ft values have led us to discuss the possible values of the 108 In and 106 In isomeric state spins [fr

Physics with isotopically controlled semiconductors

International Nuclear Information System (INIS)

Haller, E.E.

1994-08-01

Control of the isotopic composition of semiconductors offers a wide range of new scientific opportunities. In this paper a number of recent results obtained with isotopically pure as well as deliberately mixed diamond and Ge bulk single crystals and Ge isotope superlattices will be reviewed. Isotopic composition affects several properties such as phonon energies, bandstructure and lattice constant in subtle but theoretically well understood ways. Large effects are observed for thermal conductivity, local vibrational modes of impurities and after neutron transmutation doping (NTD). Several experiments which could profit greatly from isotope control are proposed

The Boron Isotopic Composition of Elephant Dung: Inputs to the Global Boron Budget

Science.gov (United States)

Williams, L. B.; Hervig, R. L.

2011-12-01

A survey of boron in kerogen showed isotopically light δ11B values (0 to -50%) that are distinctly different from most mineral and natural water B reservoirs. Diagenesis releases this isotopically light B into pore fluids when hydrocarbons are generated, thus enriching oilfield brines in 10B. This observation suggests that borated biomolecules (BM) are primarily tetrahedral favoring 10B, whereas 11B is preferred in trigonal coordination. Plants, with optimal concentrations up to 100ppm, contribute more B than animal remains to sediment. Elephants are one of the largest herbivores on earth, consuming 200 - 250 kg of plant material/day and producing 50 kg of manure/day. They are inefficient at digestion, thus the manure contains >50% undigested plant material. Dung samples are therefore ideal for studying the δ11B of both the food input and digested output of a significant B supply to sedimentary systems. Horse and rabbit manure were studied for comparison to evaluate B isotope variations in the food supply and potential vital effects on the output. B-content and isotopic composition of dung plant material and digested fractions were measured in the solid state by secondary ion mass spectrometry. The digests were rinsed in 1.8% mannitol, a B-complexing agent, to remove surface adsorbed-B, then air dried and Au-coated for charge compensation. Results showed that the elephant diet contains 3-13 ppm B, with an average δ11B of -20 ± 0.8% (1σ), while rabbit food had 88 ppm B with a δ11B of -50 ± 1.3 %. The digested fraction of the elephant dung contains 4-10ppm B with average δ11B values of -12 ± 1.2%. In comparison, horse manure with 11-21 ppm B has a δ11B of -10.7 ± 0.5% and rabbit manure contains 2-3 ppm B with a δ11B of -8.8 ± 1%. Boron isotope compositions of these manures are indistinguishable (within error). Clearly plant material is a major contributor of isotopically light B to sediments. The herbivores studied fractionate their total B intake in

What controls the stable isotope composition of precipitation in the Mekong Delta? A model-based statistical approach

Science.gov (United States)

Le Duy, Nguyen; Heidbüchel, Ingo; Meyer, Hanno; Merz, Bruno; Apel, Heiko

2018-02-01

This study analyzes the influence of local and regional climatic factors on the stable isotopic composition of rainfall in the Vietnamese Mekong Delta (VMD) as part of the Asian monsoon region. It is based on 1.5 years of weekly rainfall samples. In the first step, the isotopic composition of the samples is analyzed by local meteoric water lines (LMWLs) and single-factor linear correlations. Additionally, the contribution of several regional and local factors is quantified by multiple linear regression (MLR) of all possible factor combinations and by relative importance analysis. This approach is novel for the interpretation of isotopic records and enables an objective quantification of the explained variance in isotopic records for individual factors. In this study, the local factors are extracted from local climate records, while the regional factors are derived from atmospheric backward trajectories of water particles. The regional factors, i.e., precipitation, temperature, relative humidity and the length of backward trajectories, are combined with equivalent local climatic parameters to explain the response variables δ18O, δ2H, and d-excess of precipitation at the station of measurement. The results indicate that (i) MLR can better explain the isotopic variation in precipitation (R2 = 0.8) compared to single-factor linear regression (R2 = 0.3); (ii) the isotopic variation in precipitation is controlled dominantly by regional moisture regimes (˜ 70 %) compared to local climatic conditions (˜ 30 %); (iii) the most important climatic parameter during the rainy season is the precipitation amount along the trajectories of air mass movement; (iv) the influence of local precipitation amount and temperature is not significant during the rainy season, unlike the regional precipitation amount effect; (v) secondary fractionation processes (e.g., sub-cloud evaporation) can be identified through the d-excess and take place mainly in the dry season, either locally

Isotopic study of Karst water

International Nuclear Information System (INIS)

Leskovsek-Sefman, H.

1985-01-01

Measurement of the isotopic composition of water formed part of an extended investigation of the water drainage system in the Slovenian Karst. These studies were planned to complement geological and speleological investigations which are already being performed in this area, with the knowledge of the mechanism of changes in the isotopic composition of water in the natural environment on some smaller locations, Planina cave near Postojna where the vertical percolation of meteoric water through the karstified carbonate ceiling was studied and the water catchment areas of some small rivers, Ljubljanica, Rizana and Idrijca. Mass spectrometric investigations of the isotopic composition of some elements ( 18 O, D, 13 C and T) in water and in dissolved carbonates, as well as the isotopic composition of 18 O and 13 C in cave carbonates were performed. The results allow to conclude that the waters in karst aquifers in spite of producing the homogenisation to a great extent, qualitative determination of the retention time and of the prevailing sources for some springs and surface and underground water flows is nevertheless possible. The isotopic composition of 18 O in water and of 18 O and 13 C in dissolved carbonates depends on climatic conditions and on denudation processes. The investigation of cave carbonates revealed that they have different isotopic compositions of 18 O and 13 C because of different locations and also different ages

MEASUREMENT OF THE ISOTOPIC COMPOSITION OF HYDROGEN AND HELIUM NUCLEI IN COSMIC RAYS WITH THE PAMELA EXPERIMENT

Energy Technology Data Exchange (ETDEWEB)

Adriani, O.; Bongi, M. [Department of Physics, University of Florence, I-50019 Sesto Fiorentino, Florence (Italy); Barbarino, G. C. [Department of Physics, University of Naples ' ' Federico II' ' , I-80126 Naples (Italy); Bazilevskaya, G. A. [Lebedev Physical Institute, RU-119991, Moscow (Russian Federation); Bellotti, R.; Bruno, A. [Department of Physics, University of Bari, I-70126 Bari (Italy); Boezio, M.; Bonvicini, V.; Carbone, R. [INFN, Sezione di Trieste, I-34149 Trieste (Italy); Bogomolov, E. A. [Ioffe Physical Technical Institute, RU-194021 St. Petersburg (Russian Federation); Borisov, S.; Casolino, M.; De Pascale, M. P. [INFN, Sezione di Rome ' ' Tor Vergata' ' , I-00133 Rome (Italy); Bottai, S. [INFN, Sezione di Florence, I-50019 Sesto Fiorentino, Florence (Italy); Cafagna, F. [INFN, Sezione di Bari, I-70126 Bari (Italy); Campana, D. [INFN, Sezione di Naples, I-80126 Naples (Italy); Carlson, P. [KTH, Department of Physics, and the Oskar Klein Centre for Cosmoparticle Physics, AlbaNova University Centre, SE-10691 Stockholm (Sweden); Castellini, G. [IFAC, I-50019 Sesto Fiorentino, Florence (Italy); Danilchenko, I. A. [National Research Nuclear University MEPhI, RU-115409 Moscow (Russian Federation); De Santis, C. [Department of Physics, University of Rome ' ' Tor Vergata' ' , I-00133 Rome (Italy); and others

2013-06-10

The satellite-borne experiment PAMELA has been used to make new measurements of cosmic ray H and He isotopes. The isotopic composition was measured between 100 and 600 MeV/n for hydrogen and between 100 and 900 MeV/n for helium isotopes over the 23rd solar minimum from 2006 July to 2007 December. The energy spectrum of these components carries fundamental information regarding the propagation of cosmic rays in the galaxy which are competitive with those obtained from other secondary to primary measurements such as B/C.

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

Seasonal trends of NH4+ and NO3- nitrogen isotope composition in rain collected at Juelich, Germany

International Nuclear Information System (INIS)

Freyer, H.D.

1978-01-01

Data are presented on nitrogen isotope composition in ammonium and nitrate from rain-water collected over 2 years in an interior area at Juelich, Germany. The seasonal trends in these data are discussed relative to natural and anthropogenic emissions of nitrogen compounds which additionally have been measured or estimated in their isotope composition, e.g. ammonia from animal urine, fuel combustion, fertilizer use and organic soil nitrogen, and natural and anthropogenic nitric oxides from automobile exhausts as well. The 15 N content of Juelich rain ammonium is found to be different from values of Hoering (1957) and Moore (1974) and from other rain samples collected in coastal areas. (Auth.)

Composition-dependent trap distributions in CdSe and InP quantum dots probed using photoluminescence blinking dynamics.

Science.gov (United States)

Chung, Heejae; Cho, Kyung-Sang; Koh, Weon-Kyu; Kim, Dongho; Kim, Jiwon

2016-07-21

Although Group II-VI quantum dots (QDs) have attracted much attention due to their wide range of applications in QD-based devices, the presence of toxic ions in II-VI QDs raises environmental concerns. To fulfill the demands of nontoxic QDs, synthetic routes for III-V QDs have been developed. However, only a few comparative analyses on optical properties of III-V QDs have been performed. In this study, the composition-related energetic trap distributions have been explored by using three different types of core/multishell QDs: CdSe-CdS (CdSe/CdS/ZnS), InP-ZnSe (InP/ZnSe/ZnS), and InP-GaP (InP/GaP/ZnS). It was shown that CdSe-CdS QDs have much larger trap densities than InP-shell QDs at higher energy states (at least 1Eg (band gap energy) above the lowest conduction band edge) based on probability density plots and Auger ionization efficiencies which are determined by analyses of photoluminescence blinking dynamics. This result suggests that the composition of encapsulated QDs is closely associated with the charge trapping processes, and also provides an insight into the development of more environmentally friendly QD-based devices.

Development of a portable mass spectrometric system for determination of isotopic composition of solid uranium samples using fluorine volatilization

Science.gov (United States)

Loge, G.

1994-09-01

Using hardware and materials supplied by LANL, a prototype quadrupole mass spectrometer system designed for portable field analysis of isotopic composition of solid uranium samples was assembled and tested. The system contained the capability for fluorine volatilization of solid uranium samples with gas introduction, which was successfully tested and demonstrated using 100 mg samples of U3O8. Determination of precision and accuracy for measuring isotopic composition was performed using isotopic standards. Use with soil samples containing uranium were also attempted. Silicates in the soil forming SiF4 were found to be a kinetic bottleneck to the formation of UF6. This could be avoided by performing some sort of chemical separation as a pre-treatment step, which was demonstrated using nitric acid.

A measurement of the carbon isotopic composition in primary cosmic radiation

International Nuclear Information System (INIS)

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

1975-01-01

The isotopic composition is measured in a stack of nuclear emulsions exposed in a balloon flight from Fort Churchill. The masses of the carbon nuclei have been determined from photometric track width measurements in the residual range interval 1 13 C/( 12 C + 13 C) = 0.10 +- 0.04 at the measuring point. The result indicates that 13 C will only be present in the cosmic ray source matter in small amounts. (orig./BJ) [de

Effect of amino acids on the precipitation kinetics and Ca isotopic composition of gypsum

Science.gov (United States)

Harouaka, Khadouja; Kubicki, James D.; Fantle, Matthew S.

2017-12-01

Stirred gypsum (CaSO4 · 2H2O) precipitation experiments (initial Ωgypsum = 2.4 ± 0.14, duration ≈ 1.0-1.5 h) were conducted in the presence of the amino acids glycine (190 μM), L-alanine (190 μM), D- and L-arginine (45 μM), and L-tyrosine (200 μM) to investigate the effect of simple organic compounds on both the precipitation kinetics and Ca isotopic composition of gypsum. Relative to abiotic controls, glycine, tyrosine, and alanine inhibited precipitation rates by ∼22%, 27%, and 29%, respectively, while L- and D-arginine accelerated crystal growth by ∼8% and 48%, respectively. With the exception of tyrosine, amino acid induced inhibition resulted in fractionation factors (αs-f) associated with precipitation that were no more than 0.3‰ lower than amino acid-free controls. In contrast, the tyrosine and D- and L-arginine experiments had αs-f values associated with precipitation that were similar to the controls. Our experimental results indicate that Ca isotopic fractionation associated with gypsum precipitation is impacted by growth inhibition in the presence of amino acids. Specifically, we propose that the surface-specific binding of amino acids to gypsum can change the equilibrium fractionation factor of the bulk mineral. We investigate the hypothesis that amino acids can influence the growth of gypsum at specific crystal faces via adsorption and that different faces have distinct fractionation factors (αface-fluid). Accordingly, preferential sorption of amino acids at particular faces changes the relative, face-specific mass fluxes of Ca during growth, which influences the bulk isotopic composition of the mineral. Density functional theory (DFT) calculations suggest that the energetic favorability of glycine sorption onto gypsum crystal faces occurs in the order: (1 1 0) > (0 1 0) > (1 2 0) > (0 1 1), while glycine sorption onto the (-1 1 1) face was found to be energetically unfavorable. Face-specific fractionation factors constrained by

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.

[Determination of deuterium concentration in foods and influence of water with modified isotopic composition on oxidation parameters and heavy hydrogen isotopes content in experimental animals].

Science.gov (United States)

Basov, A A; Bykov, I M; Baryshev, M G; Dzhimak, S S; Bykov, M I

2014-01-01

The article presents the results of the study of the deuterium (D) content in food products as well as the influence of deuterium depleted water (DDW) on the concentration of heavy hydrogen isotopes in the blood and lyophilized tissues of rats. The most significant difference in the content of D was found between potato and pork fat, which indexes the standard delta notation (δ) D in promille, related to the international standard SMOW (Standard Mean Ocean of Water) amounted to -83,2 per thousand and -250,7 per thousand, respectively (phydrogen atoms in the body. The data obtained in the experimental modeling of the diet of male Wistar rats in the age of 5-6 mo (weight 235 ± 16 g) using DDW (δD = -743,2 per thousand) instead of drinking water (δD = -37,0 per thousand) with identical mineral composition showed that after 2 weeks significant (p tissue") is due to different rates ofisotopic exchange reactions in plasma and tissues (liver, kidney, heart), which can be explained by entering into the composition of a modified diet of organic substrates with more than DDW concentration D, which are involved in the construction of cellular structures and eventually lead to a redistribution of D and change direction of D/H gradient "plasmaisotopic composition, aimed at reducing the level of heavy non-radioactive atoms will allow the targeted nutritional correction of prooxidant-antioxidant status of the population in areas with adverse environmental conditions, stimulating by created isotopic D/H gradient cytoprotective mechanisms influencing the various components of nonspecific protection, including free radical oxidation processes. And then again, periodic assessment of the isotopic composition of nutrients will monitor the quality of food consumed by the population, and if

Instrumentation effects on U and Pu CBNM standards spectra quality measured on a 500 mm3 CdZnTe and a 2×2 inch LaBr3 detectors

Science.gov (United States)

Meleshenkovskii, I.; Borella, A.; Van der Meer, K.; Bruggeman, M.; Pauly, N.; Labeau, P. E.; Schillebeeckx, P.

2018-01-01

Nowadays, there is interest in developing gamma-ray measuring devices based on the room temperature operated medium resolution detectors such as semiconductor detectors of the CdZnTe type and scintillators of the LaBr3 type. This is true also for safeguards applications and the International Atomic Energy Agency (IAEA) has launched a project devoted to the assessment of medium resolution gamma-ray spectroscopy for the verification of the isotopic composition of U and Pu bearing samples. This project is carried out within the Non-Destructive Assay Working Group of the European Safeguards Research and Development Association (ESARDA). In this study we analyze medium resolution spectra of U and Pu standards with the aim to develop an isotopic composition determination algorithm, particularly suited for these types of detectors. We show how the peak shape of a CdZnTe detector is influenced by the instrumentation parameters. The experimental setup consisted of a 500 mm3 CdZnTe detector, a 2×2 inch LaBr3 detector, two types of measurement instrumentation - an analogue one and a digital one, and a set of certified samples - a 207Bi point source and U and Pu CBNM standards. The results of our measurements indicate that the lowest contribution to the peak asymmetry and thus the smallest impact on the resolution of the 500 mm3 CdZnTe detector was achieved with the digital MCA. Analysis of acquired spectra allowed to reject poor quality measurement runs and produce summed spectra files with the least impact of instrumentation instabilities. This work is preliminary to further studies concerning the development of an isotopic composition determination algorithm particularly suited for CZT and LaBr3 detectors for safeguards applications.

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

The effect of petrographical composition of coals and bituminous sediments on the material and isotopic composition of dry natural gases from artificial recoalification reactions. 2

International Nuclear Information System (INIS)

Maass, I.; Huebner, H.; Nitzsche, H.-M.; Schuetze, H.; Zschiesche, M.

1975-01-01

Experimental results indicate that on the basis of the material and isotopic composition of natural gases conclusions can be drawn with regard to the character (humic or bituminous) of the parent rock. Thus, genetic relations assumed to exist between humic sediments (e.g. coal seams) and dry natural gases as well as bituminous rocks and wet natural gases are experimentally confirmed. In addition, from analyses of the materials approximate data can be derived on the degree of carbonization of coal or bituminous sediments in the main phase of gas separation. Furthermore, these analyses were used to elucidate the question whether authochthonous or allochthonous deposits are present. It could be shown that the maceral composition of coals and of the organo-petrographical inclusions in bituminous sediments determines the isotopic composition of methane in recoalification gases to a considerable degree. (author)

Composition determination of CdS sub x Se sub 1-x mixed crystals by optical dispersion

Energy Technology Data Exchange (ETDEWEB)

Iliev, I; Dimov, T; Ribarov, D [Pedagogical High School, Schumen (Bulgaria); Lange, H [Akademie der Wissenschaften der DDR, Berlin (German Democratic Republic). Zentralinstitut fuer Elektronenphysik

1989-10-16

An optical dispersion method has been developed determining the CdS/CdSe ratio in CdS{sub x}Se{sub 1-x} mixed crystals from the relationship between position of the isotropic point (birefrigence becomes zero for a definite wavelength at the absorption edge) and chemical composition x. Birefrigence spectra and piezo-optic spectra of samples with x = 0.2, 0.6, and 0.875 give the spectral position of the isotropic point (ip). A curve of wavelength of ip versus x of CdS{sub x}Se{sub 1-x} is evaluated by the least-squares procedure and tested by X-ray fluorescence analysis.