A stable isotope study of serpentinization in the Fengtien ophiolite, Taiwan

Energy Technology Data Exchange (ETDEWEB)

Tzen-Fu Yui; Hsueh-Wen Yeh (Univ. of Hawaii, Honolulu (USA)); Chihming Wang Lee (National Taiwan Univ. (Taiwan))

1990-05-01

Detailed H- and O-isotopic studies of serpentinites of Fengtien ophiolite have been made in order to enhance our knowledge on the process of serpentinization. Pseudomorphic lizardites have {delta}{sup 18}O = +3.6{per thousand} and {delta}D = {minus}48 to {minus}49{per thousand}; bladed-mat and foliated antigorites have {delta}{sup 18}O = +3.5 to +5.8{per thousand} and {delta}D = {minus}45 to {minus}69{per thousand}; slickensided antigorites have {delta}{sup 18}O = +4.1 to +4.9{per thousand} and {delta}D = {minus}46 to {minus}50{per thousand}; picrolites have {delta}{sup 18}O = +4.2 to +4.3{per thousand} and {delta}D = {minus}65 to {minus}67{per thousand}; and slickensided chrysotiles have {delta}{sup 18}O = +4.1 to +4.5{per thousand} and {delta}D = {minus}80{per thousand}. It is suggested that lizardite might have formed in an oceanic environment, whereas antigorite and chrysotile have formed in continental environments. These results depict complicated multiple serpentinization processes. Isotopic temperatures calculated using {delta}{sup 18}O values of coexisting fissure-filling minerals range from 325 to 370{degree}C, which are consistent with those derived from phase equilibria involving serpentines. The narrow range of {delta}{sup 18}O and wide range of {delta}D values for antigorite and chrysotile also demonstrate that water/rock ratios during these serpentinizations should not have been high. These Fengtien serpentines fall outside either of the continental domains described by Wenner and Taylor (1973, 1974); and fall within their oceanic domain. We suggest that the domains proposed by Wenner and Taylor (1973, 1974) should be extended and that the terms, especially the continental antigorite and the continental lizardite-chrysotile, should be purely occurrence-descriptive.

Temperature and vital effect controls on Bamboo coral (Isididae) isotopegeochemistry: A test of the "lines method"

Energy Technology Data Exchange (ETDEWEB)

Hill, T M; Spero, H J; Guilderson, T P; LaVigne, M; Clague, D; Macalello, S; Jang, N

2011-03-01

Deep-sea bamboo corals hold promise as long-term climatic archives, yet little information exists linking bamboo coral geochemistry to measured environmental parameters. This study focuses on a suite of 10 bamboo corals collected from the Pacific and Atlantic basins (250-2136 m water depth) to investigate coral longevity, growth rates, and isotopic signatures. Calcite samples for stable isotopes and radiocarbon were collected from the base the corals, where the entire history of growth is recorded. In three of the coral specimens, samples were also taken from an upper branch for comparison. Radiocarbon and growth band width analyses indicate that the skeletal calcite precipitates from ambient dissolved inorganic carbon and that the corals live for 150-300 years, with extension rates of 9-128 {micro}m/yr. A linear relationship between coral calcite {delta}{sup 18}O and {delta}{sup 13}C indicates that the isotopic composition is influenced by vital effects ({delta}{sup 18}O:{delta}{sup 13}C slope of 0.17-0.47). As with scleractinian deep-sea corals, the intercept from a linear regression of {delta}{sup 18}O versus {delta}{sup 13}C is a function of temperature, such that a reliable paleotemperature proxy can be obtained, using the 'lines method.' Although the coral calcite {delta}{sup 18}O:{delta}{sup 13}C slope is maintained throughout the coral base ontogeny, the branches and central cores of the bases exhibit {delta}{sup 18}O:{delta}{sup 13}C values that are shifted far from equilibrium. We find that a reliable intercept value can be derived from the {delta}{sup 18}O:{delta}{sup 13}C regression of multiple samples distributed throughout one specimen or from multiple samples within individual growth bands.

Stable isotope compositions of quartz pebbles and their fluid inclusions as tracers of sediment provenance: Implications for gold- and uranium-bearing quartz pebble conglomerates

Energy Technology Data Exchange (ETDEWEB)

Vennemann, T.W.; Kesler, S.E.; O' Neil, J.R. (Univ. of Michigan, Ann Arbor (United States))

1992-09-01

Oxygen isotope compositions of pebbles from late Archean to paleo-Proterozoic gold- and/or uranium-bearing oligomictic quartz pebble conglomerates of the Witwatersrand district, South Africa, and Huronian Supergroup, Canada, were determined in an attempt to define the nature of the source terrain. The [delta][sup 18]O values of quartz pebbles within any one sample typically vary by [approximately] 4[per thousand] or more, but occasionally by as much as 8[per thousand], even for adjacent pebbles within the same hand specimen. In addition, adjacent quartz pebbles of widely contrasting [delta][sup 18]O values also preserve distinct isotopic signatures of their fluid inclusions. This overall heterogeneity suggests that the pebbles did not undergo significant oxygen isotope exchange after incorporation in the conglomerates. Therefore, oxygen isotope analyses of such quartz pebbles, in combination with a detailed investigation of their mineral and fluid inclusions, can provide a useful method for characterizing pebble populations and hence dominant sediment source modes. Comparison of values found in this study with [delta][sup 18]O values of quartz from Archean granites, pegmatites, and mesothermal greenstone gold veins, i.e., [delta][sup 18]O values of sources commonly proposed for the conglomerate ores, suggests that uranium is derived from a granitic source, whereas gold has a mesothermal greenstone gold source. Low [delta][sup 18]O values of chert pebbles (9[per thousand] to 11.5[per thousand]) relative to those expected for Archean and Proterozoic marine cherts (commonly [ge] 17[per thousand]) effectively exclude marine cherts, and therefore, auriferous iron formations and exhalatives, as likely sources of gold.

C{sub 4} plant isotopic composition ({delta}{sup 13}C) evidence for urban CO{sub 2} pollution in the city of Cotonou, Benin (West Africa)

Energy Technology Data Exchange (ETDEWEB)

Kelome, Nelly C.; Leveque, Jean; Andreux, Francis; Milloux, Marie-Jeanne [UMR Microbiologie et Geochimie des Sols INRA, Universite de Bourgogne, Centre des Sciences de la Terre, 6 Bd Gabriel, 21000 Dijon (France); Oyede, Lucien-Marc [Departement des Sciences de la Terre, Universite d' Abomey-Calavi, 01 B.P. 526, Cotonou (Benin)

2006-08-01

The carbon isotopic composition ({delta}{sup 13}C) of plants can reveal the isotopic carbon content of the atmosphere in which they develop. The {delta}{sup 13}C values of air and plants depend on the amount of atmospheric fossil fuel CO{sub 2}, which is chiefly emitted in urban areas. A new indicator of CO{sub 2} pollution is tested using the {delta}{sup 13}C variation in a C{sub 4} grass: Eleusine indica. A range of about 4%% delta units was observed at different sites in Cotonou, the largest city in the Republic of Benin. The highest {delta}{sup 13}C values, from -12%% to -14%%, were found in low traffic zones; low {delta}{sup 13}C values, from -14%% to -16%%, were found in high traffic zones. The amount of fossil fuel carbon assimilated by plants represented about 20% of the total plant carbon content. An overall decrease in plant {delta}{sup 13}C values was observed over a four-year monitoring period. This decrease was correlated with increasing vehicle traffic. The {delta}{sup 13}C dataset and the corresponding geographical database were used to map and define zones of high and low {sup 13}C-depleted CO{sub 2} emissions in urban and sub-urban areas. The spatial distribution follows dominant wind directions, with the lowest emission zones found in the southwest of Cotonou. High CO{sub 2} emissions occurred in the north, the east and the center, providing evidence of intense anthropogenic activity related to industry and transportation. (author)

C{sub 4} plant isotopic composition ((delta){sup 13}C) evidence for urban CO{sub 2} pollution in the city of Cotonou, Benin (West Africa)

Energy Technology Data Exchange (ETDEWEB)

Kelome, Nelly C.; Leveque, Jean; Andreux, Francis; Milloux, Marie-Jeanne [UMR Microbiologie et Geochimie des Sols INRA, Universite de Bourgogne, Centre des Sciences de la Terre, 6 Bd Gabriel, 21000 Dijon (France); Oyede, Lucien-Marc [Departement des Sciences de la Terre, Universite d' Abomey-Calavi, 01 B.P. 526, Cotonou (Benin)

2006-08-01

The carbon isotopic composition ((delta){sup 13}C) of plants can reveal the isotopic carbon content of the atmosphere in which they develop. The (delta){sup 13}C values of air and plants depend on the amount of atmospheric fossil fuel CO{sub 2}, which is chiefly emitted in urban areas. A new indicator of CO{sub 2} pollution is tested using the (delta){sup 13}C variation in a C{sub 4} grass: Eleusine indica. A range of about 4%% delta units was observed at different sites in Cotonou, the largest city in the Republic of Benin. The highest (delta){sup 13}C values, from -12%% to -14%%, were found in low traffic zones; low (delta){sup 13}C values, from -14%% to -16%%, were found in high traffic zones. The amount of fossil fuel carbon assimilated by plants represented about 20% of the total plant carbon content. An overall decrease in plant (delta){sup 13}C values was observed over a four-year monitoring period. This decrease was correlated with increasing vehicle traffic. The (delta){sup 13}C dataset and the corresponding geographical database were used to map and define zones of high and low {sup 13}C-depleted CO{sub 2} emissions in urban and sub-urban areas. The spatial distribution follows dominant wind directions, with the lowest emission zones found in the southwest of Cotonou. High CO{sub 2} emissions occurred in the north, the east and the center, providing evidence of intense anthropogenic activity related to industry and transportation. (author)

Simultaneous Measurement of Nitrogen and Oxygen Isotopes of Nitrate to Evaluate Nitrate Sources and Processes in Catchments

Energy Technology Data Exchange (ETDEWEB)

Ohte, Nobuhito [Graduate School of Agricultural and Life Sciences, University of Tokyo, Tokyo (Japan); Nagata, Toshi; Tayasu, Ichiro [Center for Ecological Research, Kyoto University, Ohtsu (Japan); Kyozu, Ayato; Yoshimizu, Chikage [CREST, Japan Science and Technology Agency, Center for Ecological Research, Kyoto University, Ohtsu (Japan); Osaka, Ken' ichi [Carbon and Nutrient Cycles Division, National Institute for Agro-Environmental Sciences, Tsukuba, (Japan)

2013-05-15

We review studies on applied isotope analytical techniques for identifying sources and transformations of river nitrate (NO{sub 3}{sup -}) to examine the influences of water pollution, excess nutrient (nitrogen) loads and ecosystem disturbances in river systems. We also discuss the current status and future perspectives of the application of NO{sub 3}{sup -} isotope measurements to the assessment of river nutrients. Our review shows that in recent years simultaneous measurements of nitrogen and oxygen isotopes ({delta}{sup 15}N and {delta}{sup 18}O) of NO{sub 3}{sup -} have been increasingly used to identify the sources and pathways of nitrogen in river systems. The {delta}{sup 15}N value of NO{sub 3}{sup -} is a useful indicator to evaluate the contributions of sewage and/or animal waste to NO{sub 3}{sup -} load, and the {delta}{sup 18}O value can be used for estimation of the contribution of NO{sub 3}{sup -} derived through atmospheric deposition. The microbial denitrification method is currently a most useful tool to measure the {delta}{sup 15}N and {delta}{sup 18}O values of NO{sub 3}{sup -} simultaneously, because of its capability for high throughput of samples. This method allows us to conduct a comprehensive investigation of spatial and temporal variations and mechanisms of nitrogen transport and transformation in rivers and catchments in more precise and effective manner. (author)

Pooled versus separate measurements of tree-ring stable isotopes

Energy Technology Data Exchange (ETDEWEB)

Dorado Linan, Isabel, E-mail: isabel@gfz-potsdam.de [Universitat de Barcelona, Departament d' Ecologia, Diagonal 645, 08028, Barcelona (Spain); German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany); Gutierrez, Emilia, E-mail: emgutierrez@ub.edu [Universitat de Barcelona, Departament d' Ecologia, Diagonal 645, 08028, Barcelona (Spain); Helle, Gerhard, E-mail: ghelle@gfz-potsdam.de [German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany); Heinrich, Ingo, E-mail: heinrich@gfz-potsdam.de [German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany); Andreu-Hayles, Laia, E-mail: laiandreu@ub.edu [Universitat de Barcelona, Departament d' Ecologia, Diagonal 645, 08028, Barcelona (Spain); Tree-Ring Laboratory, Lamont-Doherty Earth Observatory of Columbia University, Palisades NY (United States); Planells, Octavi, E-mail: leocarpus@hotmail.com [Universitat de Barcelona, Departament d' Ecologia, Diagonal 645, 08028, Barcelona (Spain); Leuenberger, Markus, E-mail: leuenberger@climate.unibe.ch [Climate and Environmental Physics, Physics Institute, University of Bern, Sidlerstrasse 5, 3012 Bern (Switzerland); Oeschger Centre of Climate Change Research, University of Bern, Zaehringerstrasse 25, 3012 Bern (Switzerland); Buerger, Carmen, E-mail: buerger@gfz-potsdam.de [German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany); Schleser, Gerhard, E-mail: schleser@gfz-potsdam.de [German Centre for Geosciences, Climate Dynamics and Landscape Evolution, Dendro Laboratory, Telegrafenberg, 14473, Potsdam (Germany)

2011-05-01

{delta}{sup 13}C and {delta}{sup 18}O of tree rings contain time integrated information about the environmental conditions weighted by seasonal growth dynamics and are well established as sources of palaeoclimatic and ecophysiological data. Annually resolved isotope chronologies are frequently produced by pooling dated growth rings from several trees prior to the isotopic analyses. This procedure has the advantage of saving time and resources, but precludes from defining the isotopic error or statistical uncertainty related to the inter-tree variability. Up to now only a few studies have compared isotope series from pooled tree rings with isotopic measurements from individual trees. We tested whether or not the {delta}{sup 13}C and the {delta}{sup 18}O chronologies derived from pooled and from individual tree rings display significant differences at two locations from the Iberian Peninsula to assess advantages and constraints of both methodologies. The comparisons along the period 1900-2003 reveal a good agreement between pooled chronologies and the two mean master series which were created by averaging raw individual values (Mean) or by generating a mass calibrated mean (MassC). In most of the cases, pooled chronologies show high synchronicity with averaged individual samples at interannual scale but some differences also show up especially when comparing {delta}{sup 18}O decadal to multi-decadal variations. Moreover, differences in the first order autocorrelation among individuals may be obscured by pooling strategies. The lack of replication of pooled chronologies prevents detection of a bias due to a higher mass contribution of one sample but uncertainties associated with the analytical process itself, as sample inhomogeneity, seems to account for the observed differences. - Research Highlights: {yields} Pooled {delta}{sup 13}C and {delta}{sup 18}O chronologies are expected to be similar to the mean. {yields} Empirical pooled chronologies {delta}{sup 13}C and

The Use of {delta}{sup 37}CL to Explain Origin and Production of Salt from the Saline Spring 'Fonte da Pipa' in Rio Maior (Central Portugal)

Energy Technology Data Exchange (ETDEWEB)

Eggenkamp, H. G.M.; Marques, J. M. [Centro de Petrologia e Geoquimica, Instituto Superior Tecnico, Lisbon (Portugal); Graca, H. [Centro Hospitalar das Caldas da Rainha, Caldas da Rainha (Portugal)

2013-07-15

Salt extraction in Rio Maior (Central Portugal) is unique in the sense that salt is exploited from a very saline (134 g/L NaCl) terrestrial spring. This spring receives its salt through meteoric water circulation from nearby hills along a shallow salt diapir. This is shown using {delta}{sup 37}Cl, as the composition in dug wells between the mountains and the saline spring is comparable, while {delta}{sup 37}Cl in a well to the east is significantly different. Unlike seawater this spring contains nearly pure NaCl, giving us the opportunity to determine {delta}{sup 37}Cl values in a natural salt precipitating system beyond the point where (in seawater) potassium and magnesium chlorides start to precipitate. {delta}{sup 37}Cl values were determined from brines and by precipitating salt in salt pans with different evaporation stages. Fractionation of up to 1 per mille was found. To complement these natural data, evaporation/precipitation experiments are currently being conducted under controlled laboratory conditions. First results of these experiments indicate that during continued evaporation and precipitation {delta}{sup 37}Cl continues to decrease. (author)

{Delta}{sup 14}C level of annual plants and fossil fuel derived CO{sub 2} distribution across different regions of China

Energy Technology Data Exchange (ETDEWEB)

Xi, X.T.; Ding, X.F.; Fu, D.P. [State Key Laboratory of Nuclear Physics and Technology and Institute of Heavy Ion Physics, School of Physics, Peking University, Beijing 100871 (China); Zhou, L.P. [Laboratory for Earth Surface Processes, Department of Geography, Peking University, Beijing 100871 (China); Liu, K.X., E-mail: kxliu@pku.edu.cn [State Key Laboratory of Nuclear Physics and Technology and Institute of Heavy Ion Physics, School of Physics, Peking University, Beijing 100871 (China)

2013-01-15

The {sup 14}C level in annual plants is a sensitive tracer for monitoring fossil fuel derived CO{sub 2} in the atmosphere. Corn leave samples were selected from different regions of China, including high mountains in the Tibetan Plateau, grassland in Inner Mongolia, and inland and coastal cities during the summer of 2010. The {sup 14}C/{sup 12}C ratio of the samples was measured with the NEC compact AMS system at the Institute of Heavy Ion Physics, Peking University. The fossil fuel derived CO{sub 2} was estimated by comparing the measured {Delta}{sup 14}C values of corn leave samples to background atmospheric {Delta}{sup 14}C level. The influences of topography, meteorological conditions and carbon cycling processes on the fossil fuel derived CO{sub 2} concentration are considered when interpreting the data. Our results show a clear association of the low {Delta}{sup 14}C values with regions where human activities are intensive.

Oxygen isotope geochemistry of The Geysers reservoir rocks, California

Energy Technology Data Exchange (ETDEWEB)

Gunderson, Richard P.; Moore, Joseph N.

1994-01-20

Whole-rock oxygen isotopic compositions of Late Mesozoic graywacke, the dominant host rock at The Geysers, record evidence of a large liquid-dominated hydrothermal system that extended beyond the limits of the present steam reservoir. The graywackes show vertical and lateral isotopic variations that resulted from gradients in temperature, permeability, and fluid composition during this early liquid-dominated system. All of these effects are interpreted to have resulted from the emplacement of the granitic "felsite" intrusion 1-2 million years ago. The {delta}{sup 18}O values of the graywacke are strongly zoned around a northwest-southeast trending low located near the center of and similar in shape to the present steam system. Vertical isotopic gradients show a close relationship to the felsite intrusion. The {delta}{sup 18}O values of the graywacke decrease from approximately 15 per mil near the surface to 4-7 per mil 300 to 600 m above the intrusive contact. The {delta}{sup 18}O values then increase downward to 8-10 per mil at the felsite contact, thereafter remaining nearly constant within the intrusion itself. The large downward decrease in {delta}{sup 18}O values are interpreted to be controlled by variations in temperature during the intrusive event, ranging from 150{degree}C near the surface to about 425{degree}C near the intrusive contact. The upswing in {delta}{sup 18}O values near the intrusive contact appears to have been caused by lower rock permeability and/or heavier fluid isotopic composition there. Lateral variations in the isotopic distributions suggests that the effects of temperature were further modified by variations in rock permeability and/or fluid-isotopic composition. Time-integrated water:rock ratios are thought to have been highest within the central isotopic low where the greatest isotopic depletions are observed. We suggest that this region of the field was an area of high permeability within the main upflow zone of the liquid

Proxy Records of the Indonesian Low and the El Ni{tilde n}o-Southern Oscillation (ENSO) from Stable Isotope Measurements of Indonesian Reef Corals

Energy Technology Data Exchange (ETDEWEB)

Moore, M.D.

1995-12-31

The Earth`s largest atmospheric convective center is the Indonesian Low. It generates the Australasian monsoon, drives the zonal tropospheric Walker Circulation, and is implicated in the genesis of the El Nino-Southern Oscillation (ENSO). The long-term variability of the Indonesian Low is poorly characterized, yet such information is crucial for evaluating whether changes in the strength and frequency of ENSO events are a possible manifestation of global warming. Stable oxygen isotope ratios ({delta}{sup 18}O) in shallow-water reef coral skeletons track topical convective activity over hundreds of years because the input of isotopically-depleted rainwater dilutes seawater {delta}{sup 18}O. Corals also impose a temperature-dependent fractionation on {delta}{sup 18}O, but where annual rainfall is high and sea surface temperature (SST) variability is low the freshwater flux effect dominates.

Palaeohydrological implications in the Baltic area and its relation to the groundwater at Aespoe, south-eastern Sweden - A literature study

Energy Technology Data Exchange (ETDEWEB)

Wallin, B [Geokema AB, Lidingoe (Sweden)

1995-03-01

A literature study of different groundwaters in the circum Baltic region is presented in this work. The study is mainly focused on the isotopic signatures observed in different groundwaters in Sweden and Finland. Several saline groundwaters in the Baltic region at depth of 150 to 500m depth show stable ({delta}D, {delta}{sup 13}C, {delta}{sup 18}O) and radiogenic ({delta}{sup 87}Sr) isotope assembly which is suggestive of a marine origin. However, a discrepancy is sometimes observed between the stable as well as radiogenic isotopes of the intermediate groundwater, which suggest a mixture of fossil marine water and a post-glacial runoff of melt water. In order to explain this phenomenon, the initial setting in {delta}{sup 18}O may have been depleted due to large input of high latitude marine water or cold melt waters. A solution to the contradiction between the strontium ({delta}{sup 87}Sr) and stable isotope ({delta}D, {delta}{sup 13}C, {delta}{sup 18}O) signatures of the groundwater and of the calcite fracture fillings at Aespoe and other places is attained, if it is assumed that the strontium in Baltic Sea water has undergone a significant decrease in {delta}{sup 87}Sr since the last glaciation. A scenario can be constructed to suggest that the Baltic Sea during the initial stage of the Litorina sea (8000 to 5000 Y B.P.) contained strontium with much larger {delta}{sup 87}Sr values. Another explanation for the positive {delta}{sup 87}Sr values may be due to water/rock interaction between the groundwater and the abundant fracture clay minerals, which are observed at Aespoe. Typically most of the saline groundwaters occur both in Sweden and Finland below the highest marine shore line during the Holocene. Almost all inland groundwaters show a totally different pattern which is typically non marine, meteoric in origin. (Abstract Truncated)

Spatial Distribution of Stable Isotopes of Precipitation in Kumamoto, Japan

Energy Technology Data Exchange (ETDEWEB)

Anoue, M. T.; Shimada, J. [Graduate School of Science and Technology, Kumamoto University (Japan); Ichiyanagi, K. [Graduate School of Science and Technology, Kumamoto University and Japan Agency for Marine-Earth Science and Technology (Japan)

2013-07-15

To understand the spatial distribution of stable isotopic compositions in precipitation, precipitation samples were collected every two weeks from november 2009 to december 2010 at 6 points in Kumamoto, Japan. The {delta}{sup 18}O and {delta}{sup 2}H of precipitation samples were measured by isotope ratio mass spectrometry (Delta-S) with CO{sub 2}/H2{sub O} equivalent method for {delta}{sup 18}O and the chromium reduction method for {delta}2H. The range of {delta}{sup 18}O and d-excess (= {delta}{sup 2}H - 8 {delta}{sup 18}O) in precipitation is from -13.4 per mille to -3.5 per mille and from 2.6 per mille to 35.6 per mille , respectively. Seasonal variability of {delta}{sup 18}O (d-excess) in precipitation was low (high) in winter and high (low) in summer. The seasonal wind of this study area was dominated by south-westerly in summer (from June to August) and north-westerly in winter (from December to February). These wind regimes indicate seasonal variabilities of the water vapour pathway from the origin. In this paper the trend of inland effect to the {delta}{sup 18}O for both south-westerly and north-westerly are also considered. As a result, significant correlation between distances from the coastal line at south-westerly or north-westerly and {delta}{sup 18}O in precipitation was recognized, particularly from 18 February to 7 March and from 29 September to 19 October in 2010 (statistically significant with 5% level). Furthermore, in order to evaluate the course of precipitation, the column total of water vapour flux was considered in the whole period by using JRA-25 and JCDAS. It is interesting that the inland effect corresponded to the column total of water vapour flux at south-westerly (north-westerly). Hence, it is conceivable that the spatial distribution of {delta}{sup 18}O in precipitation was controlled by a column total of water vapour flux in this area. (author)

Variation in leaf water delta D and delta 18O values during the evapotranspiration process

International Nuclear Information System (INIS)

Leopoldo, P.R.; Foloni, L.L.

1984-01-01

A theoretical model was developed to evaluate leaf water delta D and delta 18 O variation in relation to: leaf temperature, relative humidity converted to leaf temperature and delta D and delta 18 O values of atmospheric water vapour and soil water. (M.A.C.) [pt

Metabolic origin of the {delta}{sup 13}C of respired CO{sub 2} in roots of Phaseolus vulgaris

Energy Technology Data Exchange (ETDEWEB)

Bathellier, C.; Tcherkez, G.; Cornic, G.; Ghashghaie, J. [Laboratoire d' Ecologie, Systematique et Evolution - ESE, CNRS-UMR 8079 - IFR 87, Batiment 362, Universite Paris-Sud, 91405-Orsay Cedex (France); Tcherkez, G. [Plateforme Metabolisme-Metabolome, IFR87 La Plante et son Environnement, Institut de Biotechnologie des Plantes, Batiment 630, Universite Paris-Sud, 91405-Orsay Cedex (France); Bligny, R.; Gout, E. [Laboratoire de Physiologie Cellulaire Vegetale CEA-Grenoble 17, rue des Martyrs, 38054 Grenoble Cedex 9 (France)

2009-07-01

- Root respiration is a major contributor to soil CO{sub 2} efflux, and thus an important component of ecosystem respiration. But its metabolic origin, in relation to the carbon isotope composition ({delta}{sup 13}C), remains poorly understood. - Here, {sup 13}C analysis was conducted on CO{sub 2} and metabolites under typical conditions or under continuous darkness in French bean (Phaseolus vulgaris) roots. {sup 13}C contents were measured either under natural abundance or following pulse-chase labeling with {sup 13}C-enriched glucose or pyruvate, using isotope ratio mass spectrometer (IRMS) and nuclear magnetic resonance (NMR) techniques. - In contrast to leaves, no relationship was found between the respiratory quotient and the {delta}{sup 13}C of respired CO{sub 2}, which stayed constant at a low value (c. -27.5 per thousand) under continuous darkness. With labeling experiments, it is shown that such a pattern is explained by the {sup 13}C-depleting effect of the pentose phosphate pathway; and the involvement of the Krebs cycle fueled by either the glycolytic input or the lipid/protein recycling. The anaplerotic phosphoenolpyruvate carboxylase (PEPc) activity sustained glutamic acid (Glu) synthesis, with no net effect on respired CO{sub 2}. - These results indicate that the root {delta}{sup 13}C signal does not depend on the availability of root respiratory substrates and it is thus plausible that, unless the {sup 13}C photosynthetic fractionation varies at the leaf level, the root {delta}{sup 13}C signal hardly changes under a range of natural environmental conditions. (authors)

Estimation of precipitation rates by measurements of {sup 36}Cl in the GRIP ice core with the PSI/ETH tandem accelerator

Energy Technology Data Exchange (ETDEWEB)

Wagner, G.; Baumgartner, S.; Beer, J. [EAWAG, Duebendorf (Switzerland); Synal, H.A. [Paul Scherrer Inst. (PSI), Villigen (Switzerland); Suter, M. [Eidgenoessische Technische Hochschule, Zurich (Switzerland)

1997-09-01

Within the European Greenland ice core project (GRIP) {sup 36}Cl AMS measurements have been performed on ice core samples from Summit (Greenland, 73{sup o}N, 37{sup o}W). Most data analysed so far are from the lower part of the ice core. The {sup 36}Cl concentration is well correlated with {delta}{sup 18}O, which is considered as a proxy for paleotemperatures. Assuming that the deposition rate of radionuclides is independent of {delta}{sup 18}O, {sup 36}Cl is used to estimate the relationship between accumulation and {delta}{sup 18}O. The results confirm that the rapid changes of {delta}{sup 18}O, the so-called Dansgaard-Oeschger events, are also reflected in the precipitation rate. (author) 1 fig., 3 refs.

Listening in on the past: what can otolith δ18O values really tell us about the environmental history of fishes?

Science.gov (United States)

Darnaude, Audrey M; Sturrock, Anna; Trueman, Clive N; Mouillot, David; Campana, Steven E; Hunter, Ewan

2014-01-01

Oxygen isotope ratios from fish otoliths are used to discriminate marine stocks and reconstruct past climate, assuming that variations in otolith δ18O values closely reflect differences in temperature history of fish when accounting for salinity induced variability in water δ18O. To investigate this, we exploited the environmental and migratory data gathered from a decade using archival tags to study the behaviour of adult plaice (Pleuronectes platessa L.) in the North Sea. Based on the tag-derived monthly distributions of the fish and corresponding temperature and salinity estimates modelled across three consecutive years, we first predicted annual otolith δ18O values for three geographically discrete offshore sub-stocks, using three alternative plausible scenarios for otolith growth. Comparison of predicted vs. measured annual δ18O values demonstrated >96% correct prediction of sub-stock membership, irrespective of the otolith growth scenario. Pronounced inter-stock differences in δ18O values, notably in summer, provide a robust marker for reconstructing broad-scale plaice distribution in the North Sea. However, although largely congruent, measured and predicted annual δ18O values did not fully match [ corrected]. Small, but consistent, offsets were also observed between individual high-resolution otolith δ18O values measured during tag recording time and corresponding δ18O predictions using concomitant tag-recorded temperatures and location-specific salinity estimates. The nature of the shifts differed among sub-stocks, suggesting specific vital effects linked to variation in physiological response to temperature. Therefore, although otolith δ18O in free-ranging fish largely reflects environmental temperature and salinity, we counsel prudence when interpreting otolith δ18O data for stock discrimination or temperature reconstruction until the mechanisms underpinning otolith δ18O signature acquisition, and associated variation, are clarified.

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.)

Macroalgal bioindicators (growth, tissue N, {delta}{sup 15}N) detect nutrient enrichment from shrimp farm effluent entering Opunohu Bay, Moorea, French Polynesia

Energy Technology Data Exchange (ETDEWEB)

Lin, David T. [Department of Zoology, University of Hawaii at Manoa, 2538 McCarthy Mall, Edmondson 152, Honolulu, HI 96822 (United States)], E-mail: david.t.lin@ucla.edu; Fong, Peggy [Department of Ecology and Evolutionary Biology, University of California, Los Angeles, 621 Young Drive South, Los Angeles, CA 90095 (United States)

2008-02-15

Nutrient enrichment from shrimp aquaculture poses an increasing environmental threat due to the industry's projected rapid growth and unsustainable management practices. Traditional methods to monitor impacts emphasize water quality sampling; however, there are many advantages to bioindicators, especially in developing countries. We investigated the usefulness of three bioindicators-growth, tissue nitrogen content and nitrogen stable isotope signature ({delta}{sup 15}N)-in the tropical red macroalga Acanthophora spicifera. Algae were collected, cultured, and deployed in a spatial array around the outflow from a shrimp farm in Moorea, French Polynesia, to detect nitrogenous wastes. All three parameters were highest adjacent to the shrimp farm indicating nutrient enrichment, and {delta}{sup 15}N values confirmed the shrimp farm as the dominant nutrient source (5.63-5.96 per mille ). Isotope ratios proved the most sensitive indicator, as {delta}{sup 15}N signatures were detected at the most distant sites tested, confirming their usefulness in tracing nutrients and mapping the spatial extent of enrichment.

Tests of size and growth effects on Arctic charr (Salvelinus alpinus) otolith δ18 O and δ13 C values.

Science.gov (United States)

Burbank, J; Kelly, B; Nilsson, J; Power, M

2018-06-06

Otolith δ 18 O and δ 13 C values have been used extensively to reconstruct thermal and diet histories. Researchers have suggested that individual growth rate and size may have an effect on otolith isotope ratios and subsequently confound otolith based thermal and diet reconstructions. As few explicit tests of the effect of fish in freshwater environments exist, here we determine experimentally the potential for related growth rate and size effects on otolith δ 18 O and δ 13 C values. Fifty Arctic charr were raised in identical conditions for two years after which their otoliths were removed and analyzed for their δ 18 O and δ 13 C values. The potential effects of final length and the Thermal Growth Coefficient (TGC) on otolith isotope ratios were tested using correlation and regression analysis to determine if significant effects were present and to quantify effects when present. The analyses indicated that TGC and size had significant and similar positive non-linear relationships with δ 13 C values and explained 35% and 42% of the variability, respectively. Conversely, both TGC and size were found to have no significant correlation with otolith δ 18 O values. There was no significant correlation between δ 18 O and δ 13 C values. The investigation indicated the presence of linked growth rate and size effects on otolith δ 13 C values, the nature of which requires further study. Otolith δ 18 O values were unaffected by individual growth rate and size, confirming the applicability of applying these values to thermal reconstructions of fish habitat. This article is protected by copyright. All rights reserved.

Hydrogeochemical and Isotopic Characteristics of Tufa Precipitating Wates: A Case Study of the River Krka (Slovenia)

Energy Technology Data Exchange (ETDEWEB)

Zavadlav, S.; Lojen, S. [Jozef Stefan Institute, Department of Environmental Sciences, Ljubljana (Slovenia)

2013-07-15

The geochemical and stable isotope composition of tufa precipitating water in the River Krka in the Slovenian karst area were studied. Surface water chemistry in the River Krka is controlled by groundwater interactions with carbonate rocks, soil CO{sub 2} and meteoric water in the aquifer. Major element chemistry of water is controlled by dissolution of dolomite and calcite. The aquifer is the main source of cations, since concentrations of Mg{sup 2+}, Sr{sup 2+} and Ba{sup 2+} in water are highest at the spring. Ca{sup 2+} concentrations are slightly increasing due to the additional mixing of surface and groundwater downstream. Oxygen isotope composition of water indicates homogenization of meteoric water in the aquifer, while {delta}{sup 13}C values of dissolved inorganic carbon in water are affected by biological activity in the soil. {delta}{sup 18}O and {delta}{sup 13}C of bulk tufa show that deposition of tufa precipitates in the River Krka is kinetically controlled resulting in enrichment with heavier isotopes. Calculated equilibrium temperature of tufa precipitation based on the oxygen isotope composition of water and tufa fit with measured water temperature when average {delta}{sup 18}O values of water and tufa are considered. (author)

Thermal history of the unsaturated zone at Yucca Mountain, Nevada, USA

Energy Technology Data Exchange (ETDEWEB)

Whelan, Joseph F. [U.S. Geological Survey, Box 25046, M.S. 963, Denver Federal Center, Denver, CO 80225 (United States)], E-mail: jfwhelan@usgs.gov; Neymark, Leonid A.; Moscati, Richard J.; Marshall, Brian D. [U.S. Geological Survey, Box 25046, M.S. 963, Denver Federal Center, Denver, CO 80225 (United States); Roedder, Edwin [Department of Earth and Planetary Science, Harvard University, Cambridge, MA 02138 (United States)

2008-05-15

Secondary calcite, silica and minor amounts of fluorite deposited in fractures and cavities record the chemistry, temperatures, and timing of past fluid movement in the unsaturated zone at Yucca Mountain, Nevada, the proposed site of a high-level radioactive waste repository. The distribution and geochemistry of these deposits are consistent with low-temperature precipitation from meteoric waters that infiltrated at the surface and percolated down through the unsaturated zone. However, the discovery of fluid inclusions in calcite with homogenization temperatures (T{sub h}) up to {approx}80 deg. C was construed by some scientists as strong evidence for hydrothermal deposition. This paper reports the results of investigations to test the hypothesis of hydrothermal deposition and to determine the temperature and timing of secondary mineral deposition. Mineral precipitation temperatures in the unsaturated zone are estimated from calcite- and fluorite-hosted fluid inclusions and calcite {delta}{sup 18}O values, and depositional timing is constrained by the {sup 207}Pb/{sup 235}U ages of chalcedony or opal in the deposits. Fluid inclusion T{sub h} from 50 samples of calcite and four samples of fluorite range from {approx}35 to {approx}90 deg. C. Calcite {delta}{sup 18}O values range from {approx}0 to {approx}22 per mille (SMOW) but most fall between 12 and 20 per mille . The highest T{sub h} and the lowest {delta}{sup 18}O values are found in the older calcite. Calcite T{sub h} and {delta}{sup 18}O values indicate that most calcite precipitated from water with {delta}{sup 18}O values between -13 and -7 per mille , similar to modern meteoric waters. Twenty-two {sup 207}Pb/{sup 235}U ages of chalcedony or opal that generally postdate elevated depositional temperatures range from {approx}9.5 to 1.9 Ma. New and published {sup 207}Pb/{sup 235}U and {sup 230}Th/Uages coupled with the T{sub h} values and estimates of temperature from calcite {delta}{sup 18}O values indicate

Arsenic and other oxyanion-forming trace elements in an alluvial basin aquifer: Evaluating sources and mobilization by isotopic tracers (Sr, B, S, O, H, Ra)

Energy Technology Data Exchange (ETDEWEB)

Vinson, David S., E-mail: dsv3@duke.edu [Duke University, Division of Earth and Ocean Sciences, Box 90227, Durham, NC 27708 (United States); McIntosh, Jennifer C. [University of Arizona, Department of Hydrology and Water Resources, 1133 E. James E. Rogers Way, Tucson, AZ 85721 (United States); Dwyer, Gary S.; Vengosh, Avner [Duke University, Division of Earth and Ocean Sciences, Box 90227, Durham, NC 27708 (United States)

2011-08-15

Highlights: > Elevated natural As and F occur in the Willcox Basin aquifer of Arizona. > Oxyanion-forming elements are derived from volcanic-source aquifer sediments. > Sr isotopes trace sediment sources linked to oxyanion-forming trace elements. > {sup 87}Sr/{sup 86}Sr > 0.720 indicates Proterozoic crystalline-source sediment contributing low As. > Both sediment source and hydrogeochemical evolution (Ca/Na) affect As levels. - Abstract: The Willcox Basin is a hydrologically closed basin in semi-arid southeastern Arizona (USA) and, like many other alluvial basins in the southwestern USA, is characterized by oxic, near-neutral to slightly basic groundwater containing naturally elevated levels of oxyanion-forming trace elements such as As. This study evaluates the sources and mobilization of these oxyanionic trace elements of health significance by using several isotopic tracers of water-rock interaction and groundwater sources ({sup 87}Sr/{sup 86}Sr, {delta}{sup 34}S{sub SO4}, {delta}{sup 11}B, {delta}{sup 2}H, {delta}{sup 18}O, {sup 3}H). Values of {delta}{sup 2}H (-85 per mille to -64 per mille) and {delta}{sup 18}O (-11.8 per mille to -8.6 per mille) are consistent with precipitation and groundwater in adjacent alluvial basins, and low to non-detectable {sup 3}H activities further imply that modern recharge is slow in this semi-arid environment. Large variations in {sup 87}Sr/{sup 86}Sr ratios imply that groundwater has interacted with multiple sediment sources that constitute the basin-fill aquifer, including Tertiary felsic volcanic rocks, Paleozoic sedimentary rocks, and Proterozoic crystalline rocks. In general, low concentrations of oxyanion-forming trace elements and F{sup -} are associated with a group of waters exhibiting highly radiogenic values of {sup 87}Sr/{sup 86}Sr (0.72064-0.73336) consistent with waters in Proterozoic crystalline rocks in the mountain blocks (0.73247-0.75010). Generally higher As concentrations (2-29 {mu}g L{sup -1}), other

Estimation of water transit time in soils under Amazon forest cover using variations in delta18O values

International Nuclear Information System (INIS)

Leopoldo, P.R.; Matsui, E.; Salati, E.

1984-01-01

The work was carried out at the forest reserve of the Instituto Nacional de Pesquisas da Amazonia, located at km 45 of Manaus, in an area characterized by Amazon vegetation of the 'terra-firme' type. To extract the soil water, four soil-water collecting stations were installed, and in each the porous cups were placed at 15, 25, 50, 80 and 120 cm depth from the soil surface. The rain-water and soil-water samples were collected only weekly for analysis of the 18 O content. In an attempt to estimate the soil-water transit time using the variation in 18 O values, a statistical model was used. This model is based on linear regression analysis applied to the values observed for soil water and rain water. From this analysis, regression coefficients are obtained which vary according to time. The values of the coefficients obtained can be adjusted generally, according to a quadratic regression, with the maximum value of the function representing the time in which the best statistical correlation between the observed delta 18 O values occurs. The time obtained from these correlations represents the mean time necessary for the water to run from one collecting point to the next. (author)

Determination Of Oxygen Isotope Ratio (18O-/16O) and Sulfur (34S-/32S) Value Of BaSO4 Din 5033 For Internal Standard

International Nuclear Information System (INIS)

Evarista Ristin, P.I.; Sidauruk, Paston; Wibagoyo; Djiono; Satrio

2000-01-01

It has been done an experiment to determine of oxygen( 18 O-/ 16 O) and Sulfur ( 34 S-/ 32 S) ) isotop value of BaSO 4 DIN 5033 (merck) for internal standard. The used technique for preparation of CO 2 gas to measure oxygen isotop ratio ratio (stated as deltaδ 18 O) is based on Rafter on Rafte method using graphite for reduction of BaSO 4 . Where the used technique for preparation of SO 2 gas to measure isotope sulphur ratio (started as δ 34 S) is based on Robinson - Kasakabe method using Cupro oxide to oxidize Ag 2 S. The result of this experiment is 11,48±0,41 0/00 and 5,00 plus minus ±0,33 o/oo for deltaδ 18 O and δ 34 S value respectively. Based on this experiment. BaSO 4 DIN 5033 can be used as internal standard because is values both oxygen and sulphur lie in the middle of range of its variation in nature. The result of interlab comparison shows that the value of this experiment is nearly similar to the value obtained from laboratorium of Pinstech-Pakistan. To acquire the result, it is necessary to carry out more interlab comparison

Sediment features, macrozoobenthic assemblages and trophic relationships ({delta}{sup 13}C and {delta}{sup 15}N analysis) following a dystrophic event with anoxia and sulphide development in the Santa Giusta lagoon (western Sardinia, Italy)

Energy Technology Data Exchange (ETDEWEB)

Magni, P. [CNR-IAMC National Research Council - Institute for Coastal Marine Environment c/o IMC - International Marine Centre, Loc. Sa Mardini, Torregrande, 09072 Oristano (Italy); IMC - International Marine Centre, Loc. Sa Mardini, Torregrande, 09072 Oristano (Italy)], E-mail: paolo.magni@iamc.cnr.it; Rajagopal, S. [Department of Animal Ecology and Ecophysiology, Institute for Water and Wetland Research, Radboud University Nijmegen, Toernooiveld, 6525 ED Nijmegen (Netherlands); Velde, G. van der [Department of Animal Ecology and Ecophysiology, Institute for Water and Wetland Research, Radboud University Nijmegen, Toernooiveld, 6525 ED Nijmegen (Netherlands); National Museum of Natural History Naturalis, P.O. Box 9517, 2300 RA Leiden (Netherlands); Fenzi, G. [IMC - International Marine Centre, Loc. Sa Mardini, Torregrande, 09072 Oristano (Italy); Kassenberg, J. [Department of Animal Ecology and Ecophysiology, Institute for Water and Wetland Research, Radboud University Nijmegen, Toernooiveld, 6525 ED Nijmegen (Netherlands); Vizzini, S.; Mazzola, A. [Dipartimento di Biologia Animale, Universita di Palermo, via Archirafi 18, 90123 Palermo (Italy); Giordani, G. [Dipartimento di Scienze Ambientali, Universita di Parma, Via Usberti 33/A, 43100 Parma (Italy)

2008-07-01

Macrozoobenthic assemblages and stable carbon ({delta}{sup 13}C) and nitrogen ({delta}{sup 15}N) isotope values of various primary producers (macroalgae and angiosperms) and consumers (macroinvertebrate filter/suspension feeders, deposit feeders, detritivores/omnivores and carnivores and fishes) were studied in the Santa Giusta lagoon (Sardinia, Italy) before (spring) and after (autumn) a dystrophic event which occurred in the summer of 2004. A few days after the dystrophy, the physico-chemical characteristics of sediments and macrozoobenthic assemblages were also investigated. In the latter occasion, high total organic carbon (3.9%) and organic matter (15.9%) contents of surface sediments went together with peaks in acid-volatile sulphide concentrations. Certain immediate effects were quite extreme, such as the drastic reduction in macrozoobenthos and the massive fish kill in August 2004. Among the macrozoobenthos, there were few individuals of chironomid larvae and Capitella cf. capitata left. However, by October, chironomid larvae were numerous, indicating a lack of predators (e.g. fish) and competitors. In addition, some bivalve species and polychaetes which were absent, or present in small numbers before the event, became relatively numerous. The results are discussed based on a knowledge of the sulphide tolerance of these species. Stable isotope analysis clearly showed that the basal level of the food web for most consumers consisted mainly of macroalgae and sedimentary organic matter, and that the values before and after the dystrophic event were not significantly different from one another. This indicates that the relations among different trophic levels were quickly restored following the dystrophic event.

Stable isotopes and heavy metal distribution in Dreissena polymorpha (Zebra Mussels) from western basin of Lake Erie, Canada

Energy Technology Data Exchange (ETDEWEB)

Al-Aasm, I.S.; Clarke, J.D.; Fryer, B.J. [Windsor Univ., ON (Canada). Dept. of Earth Sciences

1998-02-01

Dreissena polymorpha is an exotic freshwater bivalve species which was introduced into the Great Lakes system in the fall of 1985 through the release of ballast water from European freighters. Utilizing individual growth rings of the shells, the stable isotope distribution ({delta}{sup 18}O and {delta}{sup 13}C) was determined for the life history of selected samples which were collected from the western basin of Lake Erie. These bivalves deposit their shell in near equilibrium with the ambient water and thus reflect any annual variation of the system in the isotopic records held within their shells. Observed values for {delta}{sup 18}O range from -6.64 to -9.46 permille with an average value of -7.69 permille PDB, while carbon values ranged from -0.80 to -4.67 permille with an average value of -1.76 permille PDB. Dreissena polymorpha shells incorporate metals into their shells during growth. Individual shell growth increments were analyzed for Pb, Fe, Mg, Mn, Cd, Cu, and V concentrations. The shells show increased uptake of certain metals during periods of isotopic enrichment which correspond with warmer water temperatures. Since metals are incorporated into the shells, the organism may be useful as a biomonitor of metal pollution within aquatic environments. (orig.)

Isotopic Characterization of Snow, Ice and Glacial Melt in the Western Himalayas, India

Energy Technology Data Exchange (ETDEWEB)

Rai, S. P.; Kumar, B.; Arora, M.; Singh, R. D. [National Institute of Hydrology, Roorkee, 247 667 (India)

2013-07-15

Precipitation and glacial melt samples were collected at the snout of the Gangotri Glacier, popularly known as Gaumukh, located in the western Himalayas, India. Snow and ice samples were collected from different sites of the Gangotri Glacier. The local meteoric water line (LMWL) developed for the ablation period (May to October) is {delta}{sup 2}H = 8.2 {delta}{sup 18}O + 17.1 (r{sup 2} = 0.99), which shows a slightly higher slope and intercept than GMWL. This may be due to local summer connective precipitation occurring under dry climatic conditions and mountainous region moisture recycling with the south-west monsoon. The meltwater line, {delta}{sup 2}H =9.4 {delta}{sup 18}O + 37.5 (r{sup 2}= 0.96), having a significantly higher slope and intercept than the GMWL and LMWL. The main reasons for the higher slope and intercept of meltwater line may be due to the recycling of local vapour with moisture derived from the Western disturbance moisture whose source is the Mediterranean sea. The high d-exess values of snow, ice and meltwater indicate that the source of moisture is the Western disturbances. (author)

Hot and cold CO{sub 2}-rich mineral waters in Chaves geothermal area (northern Portugal)

Energy Technology Data Exchange (ETDEWEB)

Aires-Barros, Luis; Marques, Jose Manuel; Graca, Rui Cores; Matias, Maria Jose [Universidade Tecnica de Lisboa, Lab. de Mineralogia e Petrologia (LAMPIST), Lisboa (Portugal); Weijden, Cornelis H. van der; Kreulen, Rob [Utrecht Univ., Dept. of Geochemistry, Utrecht (Netherlands); Eggenkamp, Hermanus Gerardus M. [Utrecht Univ., Dept. of Geochemistry, Utrecht (Netherlands); Reading Univ., Postgraduate Research Inst. for Sedimentology, Reading (United Kingdom)

1998-02-01

In order to update the geohydrologic characterisation of Chaves geothermal area, coupled isotopic and chemical studies have been carried out on hot and cold CO{sub 2}-rich mineral waters discharging, in northern Portugal, along one of the major regional NNE-trending faults (the so-called Verin-Chaves-Penacova Depression). Based upon their location, and chemical and isotopic composition, the analysed waters can be divided into two groups. The northern group belongs to the HCO{sub 3}/Na/CO{sub 2}-rich type, and consists of the hot spring waters of Chaves and the cold spring waters of Vilarelho da Raia. The {delta}D and {delta}{sup 18}O values show that these waters are of meteoric origin. The lack of an {sup 18}O shift indicates that there is no evidence of water/rock interaction at high temperatures. The southern group includes the cold spring waters of Campilho/Vidago and Sabroso/Pedras Salgadas. Their chemistry is similar to that of the northern group but their heavier {delta}D and {delta}{sup 18}O values could be attributed to different recharge altitudes. Mixing between deep mineralised waters and dilute superficial waters of meteoric origin might explain the higher {sup 3}H activity found in the Vidago and Pedras Salgadas mineral waters. Alternatively, they could be mainly related to shallow underground flowpaths. The {delta}{sup 13}C values support a deep-seated origin for the CO{sub 2}. The {delta}{sup 37}Cl is comparable in all the mineral waters of the study areas, indicating a common origin of Cl. The {sup 87}Sr/{sup 86}Sr ratios in waters seem to be dominated by the dissolution of plagioclases or granitic rocks. (Author)

Human impacts on groundwater flow and contamination deduced by multiple isotopes in Seoul City, South Korea

Energy Technology Data Exchange (ETDEWEB)

Hosono, Takahiro, E-mail: hosono@chikyu.ac.jp [Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047 (Japan); Ikawa, Reo, E-mail: r_ikawa@es.sci.kumamoto-u.ac.jp [Graduate School of Science and Technology, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555 (Japan); Shimada, Jun, E-mail: jshimada@sci.kumamoto-u.ac.jp [Graduate School of Science and Technology, Kumamoto University, 2-39-1 Kurokami, Kumamoto 860-8555 (Japan); Nakano, Takanori, E-mail: nakanot@chikyu.ac.jp [Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047 (Japan); Saito, Mitsuyo, E-mail: misaito@hiroshima-u.ac.jp [Graduate School of Biosphere Science, Hiroshima University, 1-7-1, Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8521 (Japan); Onodera, Shin-ichi, E-mail: sonodera@hiroshima-u.ac.jp [Graduate School of Integrated Arts and Sciences, Hiroshima University, 1-7-1, Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8521 (Japan); Lee, Kang-Kun, E-mail: kklee@snu.ac.kr [School of Earth and Environmental Science, Seoul National University, San 56-1, Shinrim-dong, Kwanak-gu, Seoul 151-747 (Korea, Republic of); Taniguchi, Makoto, E-mail: makoto@chikyu.ac.jp [Research Institute for Humanity and Nature, 457-4 Motoyama Kamigamo, Kita-ku, Kyoto 603-8047 (Japan)

2009-04-15

The influence of human activities on the flow system and contamination of groundwater were investigated in Seoul City, South Korea, one of the largest Asian cities, using a combination of isotopes ({delta}D, T, {delta}{sup 15}N, {delta}{sup 18}O, {delta}{sup 34}S, and {sup 87}Sr/{sup 86}Sr). Eighteen representative groundwater and river water samples, which were collected over a wide area of the city, were compared with previously reported data. The distribution of stable isotopes ({delta}D and {delta}{sup 18}O) with groundwater potential data shows that recharged groundwater from either the surrounding mountainous area as well as the Han River and other surface streams discharged towards the northern-central part of the city, where a subway tunnel pumping station is located. It is suggested from T values (3.3 to 5.8 T.U.) that groundwater was recharged in the last 30 to 40 years. The {delta}{sup 34}S and {delta}{sup 15}N of SO{sub 4}{sup 2-} and NO{sub 3}{sup -} data were efficiently used as indicators of contamination by human activities. These isotopes clarified that the contribution of anthropogenic contaminants i.e., industrial and household effluents, waste landfills, and fertilizers, are responsible for the enrichment by SO{sub 4}{sup 2-} (> 30 ppm as SO{sub 4}{sup 2-}) and NO{sub 3}{sup -} (> 20 ppm as NO{sub 3}{sup -}) of groundwater. The {sup 87}Sr/{sup 86}Sr values of groundwater vary (0.71326 to 0.75058) in accordance with the host rocks of different origins. Mineral elements such as Ca are also suggested to be derived naturally from rocks. The groundwater under Seoul City is greatly affected by transportation of pollutants along the groundwater flow controlled by subway tunnel pumping, contributing to the degradation of water quality in urbanized areas.

The Oxygen Isotopic Composition of Phosphate: A Tracer for Phosphate Sources and Cycling

Energy Technology Data Exchange (ETDEWEB)

Mclaughlin, K. [Southern California Coastal Water Research Project, Costa Mesa, University of California, CA (United States); Young, M. B.; Paytan, A.; Kendall, C. [U.S. Geological Survey, University of California, CA (United States)

2013-05-15

Phosphorus (P) is a limiting macro-nutrient for primary productivity and anthropogenic P-loading to aquatic ecosystems is one of the leading causes of eutrophication in many ecosystems throughout the world. Because P has only one stable isotope, traditional isotope techniques are not possible for tracing sources and cycling of P in aquatic systems. However, much of the P in nature is bonded to four oxygen (O) atoms as orthophosphate (PO{sub 4}{sup 3-}). The P-O bonds in orthophosphate are strongly resistant to inorganic hydrolysis and do not exchange oxygen with water without biological mediation (enzyme-mediated recycling). Thus, the oxygen isotopic composition of dissolved inorganic phosphate ({delta}{sup 18}O{sub p}) may be used as a tracer for phosphate sources and cycling in aquatic ecosystems. Recently, several studies have been conducted utilizing {delta}{sup 18}O{sub p} as a tracer for phosphate sources and cycling in various aquatic environments. Specifically, work to date indicates that {delta}{sup 18}O{sub p} is useful for determining sources of phosphate to aquatic systems if these sources have unique isotopic signatures and phosphate cycling within the system is limited compared to input fluxes. In addition, because various processes imprint specific fractionation effects, the {delta}{sup 18}O{sub p} tracer can be utilized to determine the degree of phosphorous cycling and processing through the biomass. This chapter reviews several of these studies and discusses the potential to utilize the {delta}{sup 18}O{sub p} of phosphate in rivers and streams. (author)

Stable Isotopes in Precipitation over Indonesia Maritime Continent

Energy Technology Data Exchange (ETDEWEB)

Ichiyanagi, K. [Graduate School of Science and Technology, Kumamoto University, and Japan Agency for Marine-Earth Science and Technology (JAMSTEC) (Japan); Suwarman, R. [Graduate School of Science and Technology, Kumamoto University (Japan); Yamanaka, M. D. [Japan Agency for Marine-Earth Science and Technology (JAMSTEC) (Japan)

2013-07-15

Daily variability of stable isotopes in precipitation was observed at 6 stations in the Indonesian Maritime Continent from 2000 to 2006. The annual mean {delta}{sup 18}O at Bukit Kototabang (GAW), Jambi, and Makassar are heavier than those for others. The precipitation amount effect was observed only at Denpasar and Makassar. There are 2 groups resulting from the local Meteoric Water line; (1) slope is nearly 7.0 and high d-excess more than 10 at GAW, Denpasar, and Manado, (2) slope is around 7.4 and low d-excess less than 7.5 per mille at Jambi, Makassar, and Palau. Seasonal variability of {delta}{sup 18}O and d-excess were classified into three patterns. There are no seasonal variations in {delta}{sup 18}O and d-excess at GAW and Jambi, but clear seasonal variations at Denpasar (DPS) and Makassar (MKS). Due to the amount effect, {delta}{sup 18}O in precipitation is high when the precipitation amount is low from May to october. In contrast, the amount effect is not significant and d-excess is constant throughout the year in Manado and Palau. The {delta}{sup 18}O in precipitation at 2 stations located in sumatra Island corresponded with the Madden-Jullian Oscillation index, while those for the other 4 stations in more easterly locations did not. This finding indicates that water vapour evaporated from the Indian Ocean can reach the Island of sumatra, but can't reach more easterly locations. (author)

Tritium contamination in [18O] water containing 18F produced by a cyclotron

International Nuclear Information System (INIS)

Ito, S.; Saze, T.; Sakane, H.; Nishizawa, K.

2003-01-01

Tritium in the target [ 18 O] water irradiated with 9.6 MeV protons for producing [ 18 F] fluoride by 18 O(p, n) 18 F reaction was predicted from the consideration on the Q value of the 18 O(p, t) 16 O reaction. A tritium beta ray spectrum was measured by a liquid scintillation counter equipped with a multichannel analyzer. The ratio of the 3 H activity to the 18 F activity in the [ 18 O] target water was 2.4x10 -6 at the beam current of 25μA. Tritium also was detected in the [ 18 O] water for recycling and the wasted acetonitrile [ 18 O] water. The purified [ 18 F]-FDG solution was not contaminated by 3 H. The 40% 3 H out of the produced activity was lost in the course of the [ 18 F]-FDG synthesis. It was suggested that 3 H evaporated into the air during [ 18 F]-FDG synthesis and caused contamination of the workroom. The radiation workers should be prevented from environmental 3 H contamination. (author)

The origins and behaviour of carbon in a major semi-arid river, the Murray River, Australia, as constrained by carbon isotopes and hydrochemistry

Energy Technology Data Exchange (ETDEWEB)

Cartwright, Ian, E-mail: ian.cartwright@monash.edu [School of Geosciences, Monash University, Clayton, Vic. 3800 (Australia)] [National Centre for Groundwater Research and Training, Flinders University, Adelaide SA 5001 (Australia)

2010-11-15

Research highlights: {yields} {delta}{sup 13}C and concentrations of DIC in Murray River controlled by mineralisation of organic carbon and evasion. {yields} Murray River is source of atmospheric CO{sub 2}. {yields} In-river processing of carbon results in difficulties in determining carbon sources. - Abstract: {delta}{sup 13}C values of dissolved inorganic C (DIC), dissolved organic C (DOC), and particulate organic C (POC) together with {delta}{sup 18}O and {delta}{sup 2}H values of water, {delta}{sup 34}S values of dissolved SO{sub 4}, and major ion concentrations were measured in the Murray River and its tributaries between November 2005 and April 2007 to constrain the origins and behaviour of riverine C. {delta}{sup 13}C{sub DIC} values in the Murray River vary between -9.5 and -4.7 per mille with a range of <3 per mille within any sampling round. {delta}{sup 13}C{sub DIC} values of the tributaries are -11.0 per mille to -5.1 per mille. DIC concentrations of the Murray River increase from {approx}25 mg/L in the middle and upper reaches of the river to 45-55 mg/L in the lower reaches. However, the mass ratio of DIC as a proportion of the total dissolved solids (TDS) decreases from {approx}0.6-0.7 in the headwaters to {approx}0.2-0.3 in the lower reaches of the river, with similar downstream changes in DIC/Cl ratios. This precludes simple evaporative concentration of DIC and is interpreted as the river evading CO{sub 2}; this interpretation is consistent with pCO{sub 2} values that are in the range 550-11,200 ppm volume (ppmv), which are far higher than those in equilibrium with the atmosphere ({approx}360 ppmv). The {delta}{sup 13}C{sub DIC} values are similar to those that would be produced by the weathering of marine limestone ({delta}{sup 13}C {approx} 0 per mille). However, the lack of marine limestones cropping out in the Murray-Darling Basin and the relatively uniform {delta}{sup 13}C{sub DIC} values of the Murray River (even in upland reaches where the

Inter- and intra-specific variability in δ13C and δ18O values of freshwater gastropod shells from Lake Lednica, western Poland

Science.gov (United States)

Apolinarska, Karina; Pełechaty, Mariusz

2017-09-01

This study focuses on the inter- and intra-specific variability in δ13C and δ18O values of shells and opercula of gastropods sampled live from the littoral zone of Lake Lednica, western Poland. The δ13C and δ18O values were measured in individual opercula of Bithynia tentaculata and in shells of Bithynia tentaculata, Gyraulus albus, Gyraulus crista, Lymnaea sp., Physa fontinalis, Radix auricularia, Theodoxus fluviatilis and Valvata cristata. The gastropods selected for the study are among the species most commonly found in European Quaternary lacustrine sediments. The carbon isotope composition of the gastropod shells was species-specific and the same order of species from the most to the least 13C-depleted was observed at all sites sampled. Differences in shell δ13C values between species were similar at all sampling sites, thus the factors influencing shell isotopic composition were interpreted as species-specific. The δ18O values of shells were similar in all the species investigated. Significant intra-specific variability in shell δ13C and δ18O values was observed not only within the populations of Lake Lednica, which can be explained by heterogeneity of δ13C DIC, δ18O water and water temperature between the sites where macrophytes with snails attached were sampled, but also between individuals sampled from restricted areas of the lake's bottom. The latter points to the importance of factors related to the ontogeny of individual gastropods.

Stable isotope geochemistry of deep sea cherts

Energy Technology Data Exchange (ETDEWEB)

Kolodny, Y; Epstein, S [California Inst. of Tech., Pasadena (USA). Div. of Geological Sciences

1976-10-01

Seventy four samples of DSDP (Deep Sea Drilling Project) recovered cherts of Jurassic to Miocene age from varying locations, and 27 samples of on-land exposed cherts were analyzed for the isotopic composition of their oxygen and hydrogen. These studies were accompanied by mineralogical analyses and some isotopic analyses of the coexisting carbonates. delta/sup 18/0 of chert ranges between 27 and 39 parts per thousand relative to SMOW, delta/sup 18/0 of porcellanite - between 30 and 42 parts per thousand. The consistent enrichment of opal-CT in porcellanites in /sup 18/0 with respect to coexisting microcrystalline quartz in chert is probably a reflection of a different temperature (depth) of diagenesis of the two phases. delta/sup 18/0 of deep sea cherts generally decrease with increasing age, indicating an overall cooling of the ocean bottom during the last 150 m.y. A comparison of this trend with that recorded by benthonic foraminifera (Douglas et al., Initial Reports of the Deep Sea Drilling Project; 32:509(1975)) indicates the possibility of delta/sup 18/0 in deep sea cherts not being frozen in until several tens of millions of years after deposition. Cherts of any Age show a spread of delta/sup 18/0 values, increasing diagenesis being reflected in a lowering of delta/sup 18/0. Drusy quartz has the lowest delta/sup 18/0 values. On land exposed cherts are consistently depleted in /sup 18/0 in comparison to their deep sea time equivalent cherts. Water extracted from deep sea cherts ranges between 0.5 and 1.4 wt%. deltaD of this water ranges between -78 and -95 parts per thousand and is not a function of delta/sup 18/0 of the cherts (or the temperature of their formation).

Isotopic Composition and Age of Surface Water as Indicators of Groundwater Sustainability in a Semiarid Area: Case of the Souss Basin (Morocco)

Energy Technology Data Exchange (ETDEWEB)

Bouchaou, L.; Tagma, T.; Boutaleb, S.; Hsissou, Y. [LAGAGE Laboratory, Ibn Zohr University, Agadir (Morocco); Nathaniel, W.; Vengosh, A. [Duke University (United States); Michelot, J. L.; Massault, M. [UMR ' IDES' , CNRS - Universite Paris-Sud, Orsay (France); Elfaskaoui, M. [Hydraulic Agency of Souss-Massa-Draa Basins, Agadir (Morocco)

2013-07-15

This study aims to determine the surface water and groundwater interconnection in the Souss catchment of western Morocco by applying multiple isotopic tracers such as {delta}{sup 18}O, {delta}{sup 2}H, {sup 3}H, Ra, {sup 14}C, {sup 87}Sr/{sup 86}Sr and CFCs. Stable water isotope data indicate that the High Atlas Mountains, with their high rainfall and low {delta}{sup 18}O and {delta}{sup 2}H values, constitute the major source of recharge to the Souss-Massa aquifer. Carbon-{sup 14} activities (34-94 pMC) and {sup 3}H indicate a long residence time of groundwater in some areas. The high {sup 14}C activities measured in the Ifni spring located at 2158 m a.s.l. and the Tiar spring at 711 m a.s.l. indicate a modern contribution, which is consistent with recharge from the High Atlas tributaries. In the upstream mountainous section, the mass balance mixing model suggest that groundwater contribution to stream flow is about 72% during the wet season and 36% during the dry season. In the downstream plain, 80% of surface flow infiltrates to the aquifer. {sup 226}Ra and {sup 87}Sr/{sup 86}Sr variations were indistinguishable for surface waters and groundwater. (author)

First field-based observations of δ2H and δ18O values of precipitation and other water bodies in the Mongolian Gobi desert

Science.gov (United States)

Burnik Šturm, Martina; Ganbaatar, Oyunsaikhan; Voigt, Christian C.; Kaczensky, Petra

2017-04-01

Hydrogen (δ2H) and oxygen (δ18O) isotope values of water are widely used to track the global hydrological cycle and the global δ2H and δ18O patterns of precipitation are increasingly used in studies on animal migration, forensics, food authentication and traceability studies. However, δ2H and δ18O values of precipitation spanning one or more years are available for only a few 100 locations worldwide and for many remote areas such as Mongolia data are still scarce. We obtained the first field-based δ2H and δ18O isotope data of event-based precipitation, rivers and other water bodies in the extreme environment of the Dzungarian Gobi desert in SW Mongolia, covering a period of 16 months (1). Our study area is located over 450 km north-east from the nearest IAEA GNIP station (Fukang station, China) from which it is separated by a mountain range at the international border between China and Mongolia. Isotope values of the collected event-based precipitation showed and extreme range and a high seasonal variability with higher and more variable values in summer and lower in winter. The high variability could not be explained by different origin of air masses alone (i.e. NW polar winds over Russia or westerlies over Central Asia; analyzed using back-trajectory HYSPLIT model), but is likely a result of a combination of different processes affecting the isotope values of precipitation in this area. The calculated field-based local meteoric water line (LMWL, δ2H=(7.42±0.16)δ18O-(23.87±3.27)) showed isotopic characteristics of precipitation in an arid region. We observed a slight discrepancy between the filed based and modelled (Online Isotope in Precipitation Calculator, OIPC) LMWL which highlighted the difficulty of modelling the δ2H and δ18O values for areas with extreme climatic conditions and thus emphasized the importance of collecting long-term field-based data. The collected isotopic data of precipitation and other water bodies provide a basis for future

The use of 18O as a groundwater tracer in the Marlborough Region

International Nuclear Information System (INIS)

Stewart, M.K.

2006-01-01

The usefulness of 18 O for monitoring groundwater wells in the Wairau River coastal plain has been investigated by conducting a survey of the wells used for monitoring. The δ 18 O values of the Wairau Aquifer well waters show trends along the lines of flow depending on distance and depth. Near the head of the valley and close to the river, the groundwater has δ 18 O values like that of the Wairau River. With distance from the river and towards the coast, the δ 18 O values of shallow groundwater in the unconfined aquifer become more positive as land surface infiltrating recharge with higher δ 18 O values contributes to the flow. The infiltrating water also carries nitrate and other chemicals to the groundwater. At deeper levels, the groundwater is not affected by water infiltrating through the surface, and retains its Wairau River δ 18 O signature when it rises towards the surface near the coast. However, this conclusion is regarded as preliminary because of the possible temporal variability of the groundwater δ 18 O values. Regular 3-monthly 18 O measurements should be carried out on 8 key wells to substantiate this conclusion. The δ 18 O values of the southern valley aquifer waters indicate that they are sourced from local streams and surface recharge. The Rarangi and Tuamarina aquifers are sourced from local rainfall with δ 18 O of -6.2 permille. (author). 5 refs., 3 figs., 2 tabs

Variation of the 18O/16O ratio in water samples from branches

International Nuclear Information System (INIS)

Foerstel, H.; Huetzen, H.

1979-06-01

The studies of the water turnover of plants may use the labelling of water by its natural variation of the 18 O/ 16 O ratio. The basic value of such a study is the isotope ratio in soil water, which is represented by the 18 O/ 16 O ratio in water samples from stem and branches, too. During the water transport from the soil water reservoir to the leaves of trees, no fractionation of the oxygen isotopes occurs. The oxygen isotope ratio within a single twig varies about +- 0 / 00 (variation given as standard deviation of the delta-values), within the stem of a large tree about +- 2 0 / 00 . The results of water from stems of different trees at the site of the Nuclear Research Center Juelich scatter about +- 1 0 / 00 . The delta-values from a larger area (Rur valley-Eifel hills-Mosel valley), which were collected in October 1978 during the end of the vegetation period, showed a standard deviation between +- 2.2 (Rur valley) and +- 3.6 0 / 00 (Eifel hills). The 18 O/ 16 O-delta-values of a beech wood from Juelich site are in the range of - 7.3 and - 10.1 0 / 00 (mean local precipitation 1974 - 1977: - 7.4 0 / 00 ). At the hill site near Cologne (Bergisches Land, late September 1978) we observed an oxygen isotope ratio of - 9.1 0 / 00 (groundwater at the neighbourhood between - 7.6 and 8.7 0 / 00 ). In October 1978 at an area from the Netherlands to the Mosel valley we found delta-values of branch water between - 13.9 (lower Ruhr valley) and - 13.1 (Eifel hills to Mosel valley) in comparison to groundwater samples from the same region: - 7.55 and - 8.39. There was no significant difference between delta-values from various species or locations within this area. Groundwater samples should normally represent the 18 O/ 16 O ratio of local precipitation. The low delta-values of branch water could be due to the rapid uptake of precipitation water of low 18 O content in autumn to the water transport system of plants. (orig.) [de

Flow of river water into a Karstic limestone aquifer. 1. Tracing the young fraction in groundwater mixtures in the Upper Floridan Aquifer near Valdosta, Georgia

Energy Technology Data Exchange (ETDEWEB)

Plummer, L.N.; Busenberg, E. [U.S. Geological Survey, 432 National Center, Reston, VA (United States); McConnell, J.B. [U.S. Geological Survey, 3039 Amwiler Rd., Atlanta, GA (United States); Drenkard, S.; Schlosser, P. [Lamont-Doherty Earth Observatory of Columbia University, 61 Route 9W, Palisades, NY (United States); Michel, R.L. [U.S. Geological Survey, Mail Stop 434, 345 Middlefield Road, Menlo Park, CA (United States)

1998-11-01

he quality of water in the Upper Floridan aquifer near Valdosta, Georgia is affected locally by discharge of Withlacoochee River water through sinkholes in the river bed. Data on transient tracers and other dissolved substances, including Cl{sup -}, {sup 3}H, tritiogenic helium-3 ({sup 3}He), chlorofluorocarbons (CFC-11, CFC-12, CFC-113), organic C (DOC), O{sub 2} (DO), H{sub 2}S, CH{sub 4}, {delta}{sup 18}O, {delta}D, and {sup 14}C were investigated as tracers of Withlacoochee River water in the Upper Floridan aquifer. The concentrations of all tracers were affected by dilution and mixing. Dissolved Cl{sup -}, {delta}{sup 18}O, {delta}D, CFC-12, and the quantity ({sup 3}H+{sup 3}He) are stable in water from the Upper Floridan aquifer, whereas DOC, DO, H{sub 2}S, CH{sub 4}, {sup 14}C, CFC-11, and CFC-113 are affected by microbial degradation and other geochemical processes occurring within the aquifer. Groundwater mixing fractions were determined by using dissolved Cl{sup -} and {delta}{sup 18}O data, recognizing 3 end-member water types in the groundwater mixtures: (1) Withlacoochee River water ({delta}{sup 18}O=-2.5{+-}0.3per thousand, Cl{sup -}=12.2{+-}2 mg/l), (2) regional infiltration water ({delta}{sup 18}O=-4.2{+-}0.1per thousand, Cl{sup -}=2.3{+-}0.1 mg/l), and (3) regional paleowater resident in the Upper Floridan aquifer ({delta}{sup 18}O=-3.4{+-}0.1per thousand, Cl{sup -}=2.6{+-}0.1 mg/l) (uncertainties are {+-}1{sigma}). Error simulation procedures were used to define uncertainties in mixing fractions. Fractions of river water in groundwater range from 0 to 72% and average 10%. The influence of river-water discharge on the quality of water in the Upper Floridan aquifer was traced from the sinkhole area on the Withlacoochee River 25 km SE in the direction of regional groundwater flow. Infiltration of water is most significant to theN and NW of Valdosta, but becomes negligible to the S and SE in the direction of general thickening of post-Eocene confining

Petrogenesis of low-δ18O quartz porphyry dykes, Koegel Fontein complex, South Africa

Science.gov (United States)

Harris, Chris; Mulder, Kwenidyn; Sarkar, Saheli; Whitehead, Benjamin; Roopnarain, Sherissa

2018-04-01

This paper investigates the origin of low-δ18O quartz porphyry dykes associated with the 144-133 Ma Koegel Fontein Igneous Complex, which was intruded during the initial phase of breakup of Africa and South America. The 25-km diameter Rietpoort Granite is the largest and youngest phase of activity, and is roofed by a 10-km diameter pendant of gneiss. Quartz porphyry (QP) dykes, up to 15 m in width, strike NW-SE across the complex. The QP dykes that intruded outside the granite have similar quartz phenocryst δ18O values (average 8.0‰, ± 0.7, n = 33) to the granite (average 8.3 ± 1.0, n = 7). The QP dykes that intruded the roof pendant have quartz phenocrysts with more variable δ18O values (average 1.6‰, ± 2.1, n = 55). In some cases quartz phenocrysts have δ18O values as low as - 2.5‰. The variation in δ18O value within the quartz crystal population of individual dykes is small relative to the overall range, and core and rim material from individual quartz phenocrysts in three samples are identical within error. There is no evidence that quartz phenocryst δ18O values have been affected by fluid-rock interaction. Based on a Δquartz-magma value of 0.6‰, magma δ18O values must have been as low as - 3.1‰. Samples collected along the length of the two main QP dykes that traverse the roof pendant have quartz phenocryst δ18O values that range from + 1.1 to + 4.6‰, and - 2.3 to + 5.6‰, respectively. These δ18O values correlate negatively ( r = - 0.96) with initial 87Sr/86Sr, which can be explained by the event that lowered δ18O values of the source being older than the dykes. We suggest that the QP dykes were fed by magma produced by partial melting of gneiss, which had been variably altered at high temperature by 18O-depleted meteoric water during global glaciation at 550 Ma. The early melts had variable δ18O value but as melt pockets interconnected during melting, the δ18O values approached that of average gneiss. Variable quartz phenocryst �

On the Isotopic Altitude Effect of Precipitation in the Northern Adriatic (Croatia)

Energy Technology Data Exchange (ETDEWEB)

Roller-Lutz, Z.; Mance, D.; Hunjak, T., E-mail: Roller@medri.hr [Stable Isotope Laboratory, Medical Faculty, University of Rijeka, Rijeka (Croatia); Lutz, H. O. [Stable Isotope Laboratory, Medical Faculty, University of Rijeka, Rijeka (Croatia); Physics Faculty, Bielefeld University, Bielefeld (Germany)

2013-07-15

The upper (northern) Adriatic is very rich in precipitation. This input into the water system and its stable isotope composition is a basic factor, knowledge of which is required for proper use and management of water resources. The geomorphology of the region (e.g., mountains of 1400 m next to the sea) can cause specific local conditions. The isotopic composition of precipitation has been measured in various locations at different altitudes. For {delta}{sup 18}O this 'altitude effect' is found to lie around -0.2 per mille /100 m; its exact value depends on the specific location and the season. The {delta}{sup 2}H values and the d-excess vary correspondingly. (author)

Biogeochemical cycling of arsenic in coastal salinized aquifers: Evidence from sulfur isotope study

Energy Technology Data Exchange (ETDEWEB)

Kao, Yu-Hsuan [Department of Bioenvironmental Systems Engineering, National Taiwan University, Taipei 106, Taiwan, ROC (China); Wang, Sheng-Wei [Agricultural Engineering Research Center, Chungli 320, Taiwan, ROC (China); Liu, Chen-Wuing, E-mail: lcw@gwater.agec.ntu.edu.tw [Department of Bioenvironmental Systems Engineering, National Taiwan University, Taipei 106, Taiwan, ROC (China); Wang, Pei-Ling [Institute of Oceanography, National Taiwan University, Taipei 106, Taiwan, ROC (China); Wang, Chung-Ho [Institute of Earth Sciences, Academia Sinica, Taipei 115, Taiwan, ROC (China); Maji, Sanjoy Kumar [Department of Bioenvironmental Systems Engineering, National Taiwan University, Taipei 106, Taiwan, ROC (China)

2011-10-15

Arsenic (As) contamination of groundwater, accompanied by critical salinization, occurs in the southwestern coastal area of Taiwan. Statistical analyses and geochemical calculations indicate that a possible source of aqueous arsenic is the reductive dissolution of As-bearing iron oxyhydroxides. There are few reports of the influence of sulfate-sulfide redox cycling on arsenic mobility in brackish groundwater. We evaluated the contribution of sulfate reduction and sulfide re-oxidation on As enrichment using {delta}{sup 34}S{sub [SO{sub 4]}} and {delta}{sup 18}O{sub [SO{sub 4]}} sulfur isotopic analyses of groundwater. Fifty-three groundwater samples were divided into groups of high-As content and salinized (Type A), low-As and non-salinized (Type B), and high-As and non-salinized (Type C) groundwaters, based on hydro-geochemical analysis. The relatively high enrichment of {sup 34}S{sub [SO{sub 4]}} and {sup 18}O{sub [SO{sub 4]}} present in Type A, caused by microbial-mediated reduction of sulfate, and high {sup 18}O enrichment factor ({epsilon}{sub [SO{sub 4-H{sub 2O]}}}), suggests that sulfur disproportionation is an important process during the reductive dissolution of As-containing iron oxyhydroxides. Limited co-precipitation of ion-sulfide increased the rate of As liberation under anaerobic conditions. In contrast to this, Type B and Type C groundwater samples showed high {delta}{sup 18}O{sub [SO{sub 4]}} and low {delta}{sup 34}S{sub [SO{sub 4]}} values under mildly reducing conditions. Base on {sup 18}O mass balance calculations, the oxide sources of sulfate are from infiltrated atmospheric O{sub 2}, caused by additional recharge of dissolved oxygen and sulfide re-oxidation. The anthropogenic influence of extensive pumping also promotes atmospheric oxygen entry into aquifers, altering redox conditions, and increasing the rate of As release into groundwater. - Highlights: {yields} Seawater intrusion and elevated As are the main issues of groundwater in Taiwan

Carbon and oxygen isotopes in carbonatites from Puna, Jujuy and Salta, Argentina; Isotopos de carbono y oxigeno en carbonatitas en la Puna Oriental, Provincias de Jujuy y Salta, Republica Argentina

Energy Technology Data Exchange (ETDEWEB)

Zappettini, Eduardo O; Rubiolo, Daniel [Servicio Geologico Minero Argentino (SEGEMAR), Buenos Aires (Argentina). Instituto de Geologia y Recursos Naturales; Hubberten, Hans W [Alfred-Wegener-Institut fuer Polar- und Meeresforschung, Bremerhaven (Germany)

1998-07-01

{delta}{sup 13} and {delta}{sup 18}O data from carbonatites indicate that bodies formed by crystallization of carbonate magma with subsequent formation of metasomatic and hydrothermal carbonatitic veins. The isotopic data are consistent with the available geochemical and petrologic information. (author)

A study of the process of joint formation of methane gas-hydrate and authigenic carbonates in bottom sediments in the Sea of Okhotsk

Energy Technology Data Exchange (ETDEWEB)

Esikov, A D [AN SSSR, Moscow (USSR). Water Problems Inst.; Pashkina, V I [AN SSSR, Moscow (USSR). Inst. Okeanologii

1990-01-01

The discovery of gas-hydrates in bottom sediments in the Sea of Okhotsk has allowed isotope fractionation of oxygen and hydrogen to be determined in the formation of the crystal lattice. It was established that the structure of gas-hydrate selectively included the heavier isotopes of oxygen and hydrogen, so that the gas-hydrate water had values of {delta}{sup 18}O = +1.9 per mille and {delta}D = +23 per mille, whereas the interstitial water was ''lighter'' in isotopes, with the values of {delta}{sup 18}O = -0.5 per mille and {delta}D = -5 per mille (relative to SMOW (standard mean ocean water)). The formation of gas-hydrates under the conditions of underwater discharge of methane alters the chemical composition of interstitial water, so that the carbonate equilibrium is shifted, and carbonates of authigenic origin are formed. The isotope composition of the carbonates is characterized by a low content of {sup 13}C({delta}{sup 13}C from -39.3 to -51.8 per mille PDB) and a high content of {sup 18}O({delta}{sup 18}O from + 2.7 to +6.3 per mille PDB) in comparison with carbonates of sea origin. These characteristics of the isotope composition suggest the participation of methane in the formation of authigenic carbonates, due to its anaerobic oxidation and the involvement of sulfate in the silt water. (author).

18O/16O ratios of the pore water of Baltic Sea sediments

International Nuclear Information System (INIS)

Foerstel, H.

1983-01-01

Two cores of Baltic Sea sediment were collected in 1975. The 18 O/ 16 O ratio of the water enclosed in the sediment (pore water) was measured after the separation of the liquid from the solid phase. The results may support the discussion about the history of the Baltic Sea. At the top of the core the 18 O/ 16 O ratio of the water represents the oxygen isotope composition of the sea water above. Towards the deeper parts of the sediment, independently of the salt content, the 18 O/ 16 O ratio decreases towards values observed in the precipitation of the surrounding land areas. (author)

Study of some direct reactions at 00 in 18O+26Mg and 18O+12C systems

International Nuclear Information System (INIS)

Payet, J.

1984-01-01

Direct transfer reactions induced by a 18 O beam on 12 C and 26 Mg targets, have been studied at the MP tandem (Orsay) with an experimental set up giving the possibility to have angular distributions up to 0 0 . Transfer reactions to discrete levels were analysed in the D.W.B.A. framework. This analysis confirms the interest as a spectroscopic tool of this 0 0 measurements. The ( 18 O, 16 O) and ( 18 O, 20 Ne) reactions were observed up to 40 MeV excitation energy. A diffractionnal model, including the one step direct transfer hypothesis, gives a qualitative agreement with the angular distributions and the energy spectra. A parametrization of a specific small angles development of the transfer amplitudes does not give good results with physical values for the parameters. 32 refs [fr

Gaining insight into Clipperton's lagoon hydrology using tritium

Energy Technology Data Exchange (ETDEWEB)

Jean-Baptiste, P.; Fourre, E. [CEA Saclay, LSCE, CEA CNRS IPSL, F-91191 Gif Sur Yvette, (France); Charlou, J.L.; Donval, J.P. [IFREMER, Ctr Brest, DRO GM, Plouzane, (France); Correge, T. [Univ Bordeaux 1, CNRS, UMR 5805, F-33405 Talence, (France)

2009-07-01

Historical descriptions of the Clipperton lagoon appear to converge on the fact that it became isolated from the surrounding ocean around 1858. Since then, because of the high precipitation rate which largely exceeds evaporation in this region of the eastern tropical Pacific, a brackish lens has formed on top of the saline oceanic waters. In 1980, literature data show that the thickness of this water body was reaching 14 m. During the 2005 Etienne's Clipperton expedition, we collected lagoon water on two vertical profiles. Salinity, {delta}{sup 18}O and tritium analyses were performed on these samples with the objective of gaining further insight into the lagoon hydrology and age of the deep waters. The upper 15 m were characterized by low salinities (5.4 {+-} 0.2), and {delta}{sup 18}O and tritium values typical of local precipitation. At depth, waters had salinity and {delta}{sup 18}O similar to oceanic surface waters but with low tritium concentrations, hence pointing to quite isolated waters representing a remnant of marine waters when the lagoon was still communicating with the ocean. At lagoon closure, the excess of precipitation over evaporation raised the lagoon level, thus creating a hydraulic pressure head which favored salt expulsion through the permeable walls of the atoll. A simple geohydrological modeling of this salt expulsion process based on Darcy's law describes reasonably well the time-evolution of the brackish lens. Tritium is used to discuss the main physical processes potentially involved in the slow ventilation of the halo-cline and deep saline layer, including vertical diffusion, sinking of salty Surface water intrusions and deep horizontal exchange through fissures in the limestone. These different mechanisms give reasonable results, which are all compatible with available salinity and isotopic data ({delta}{sup 18}O and tritium), and therefore are all plausible candidates. Unfortunately, the lack of a detailed description of the

Salinity information in coral δ18O records

Science.gov (United States)

Conroy, J. L.; Thompson, D. M.; Dassié, E. P.; Stevenson, S.; Konecky, B. L.; DeLong, K. L.; Sayani, H. R.; Emile-Geay, J.; Partin, J. W.; Abram, N. J.; Martrat, B.

2017-12-01

Coral oxygen isotopic ratios (δ18O) are typically utilized to reconstruct sea surface temperature (SST), or SST-based El Niño-Southern Oscillation metrics (e.g., NIÑO3.4), despite the influence of both SST and the oxygen isotopic composition of seawater (δ18Osw) on coral δ18O. The ideal way to isolate past δ18Osw variations is to develop independent and univariate SST and δ18Osw responders, for instance, via paired coral δ18O and Sr/Ca analyses. Nonetheless, many coral δ18O records without paired Sr/Ca records already exist in the paleoclimatic literature, and these may be able to provide some insight into past δ18Osw and salinity changes due to the nature of the significant positive relationship between instrumental salinity and δ18Osw. Here we use coral δ18O records from the new PAGES Iso2k database to assess the regions in which coral δ18O has the greatest potential to provide salinity information based on the strength of the relationship between instrumental salinity and coral δ18O values. We find from annual pseudocoral similations that corals in the western tropical Pacific share a substantial fraction of their variance with δ18Osw rather than SST. In contrast, in the Indian Ocean and eastern tropical Pacific it is SST that predominantly explains coral δ18O variance. In agreement with this variance decomposition, we find that coral δ18O time series from the western tropical Pacific are significantly correlated with mid to late 20th century salinity. However, variations in the strength of the δ18Osw-salinity relationship across the western tropical Pacific will likely have a significant influence on coral δ18O-based salinity reconstructions. Additionally, in some cases a strong, negative correlation between SST and δ18Osw might not allow their influences to be adequately separated in coral δ18O records without the use of coupled Sr/Ca estimates of the temperature contribution. Overall, we find a range of modern salinity and SST

Effects of variation in background mixing ratios of N2, O2, and Ar on the measurement of δ18O-H2O and δ2H-H2O values by cavity ring-down spectroscopy

Science.gov (United States)

Johnson, Jennifer E.; Rella, Chris W.

2017-08-01

Cavity ring-down spectrometers have generally been designed to operate under conditions in which the background gas has a constant composition. However, there are a number of observational and experimental situations of interest in which the background gas has a variable composition. In this study, we examine the effect of background gas composition on a cavity ring-down spectrometer that measures δ18O-H2O and δ2H-H2O values based on the amplitude of water isotopologue absorption features around 7184 cm-1 (L2120-i, Picarro, Inc.). For background mixtures balanced with N2, the apparent δ18O values deviate from true values by -0.50 ± 0.001 ‰ O2 %-1 and -0.57 ± 0.001 ‰ Ar %-1, and apparent δ2H values deviate from true values by 0.26 ± 0.004 ‰ O2 %-1 and 0.42 ± 0.004 ‰ Ar %-1. The artifacts are the result of broadening, narrowing, and shifting of both the target absorption lines and strong neighboring lines. While the background-induced isotopic artifacts can largely be corrected with simple empirical or semi-mechanistic models, neither type of model is capable of completely correcting the isotopic artifacts to within the inherent instrument precision. The development of strategies for dynamically detecting and accommodating background variation in N2, O2, and/or Ar would facilitate the application of cavity ring-down spectrometers to a new class of observations and experiments.

Assessing Covariation of Holocene Monsoon Intensity and Local Moisture Conditions in Eastern and Southwestern Amazon Basin Using Speleothem δ18O and 87Sr/86Sr Values

Science.gov (United States)

Ward, B. M.; Wong, C. I.; Novello, V. F.; Silva, L.; McGee, D.; Cheng, H.; Wang, X.; Edwards, R. L.; Cruz, F. W., Sr.; Santos, R. V.

2017-12-01

δ18O records from South America offer insight into past variability of the South American Monsoon System (SAMS). Potential, however, for understanding local moisture conditions is limited as precipitation δ18O is strongly influenced by regional climate dynamics. Here we create Holocene speleothem 87Sr/86Sr records at 200-yr resolution using TIMS methods in the Center for Isotope Geochemistry at Boston College to complement existing Holocene δ18O speleothem records and investigate local moisture conditions above caves located in the eastern Amazon Basin (PAR - 4°S, 55°W) and southwestern Brazil (JAR - 21°S, 56°W). Speleothem 87Sr/86Sr variability is interpreted to reflect differences in the extent of water-rock interaction due to differences in infiltration rates under wet and dry conditions. Drier conditions promote longer residence time, enhanced water-rock interaction, and greater evolution of dripwater 87Sr/86Sr values from an initial isotopic signature acquired from the soil to the signature of the cave host rock. PAR speleothem 87Sr/86Sr values range from 0.71024 to 0.71067 and are bracketed by soil (0.71710 to 0.70956) and bedrock (0.70852 to 0.70899) values. JAR speleothem 87Sr/86Sr values range from 0.71216 to 0.71539 and are greater than bedrock values (0.70825 to 0.71219), although some speleothem values exceed the single analysis conducted of the soil isotopic composition (0.71473). JAR speleothem 87Sr/86Sr values increase from the early to mid Holocene, consistent with increase in local moisture availability associated with intensification of the SAMS suggested by decreasing δ18O values in many records from the region. Speleothem 87Sr/86Sr values at JAR decrease from the mid to late Holocene, consistent with an increase in δ18O values at PAR that suggest a decline in monsoon intensity. 87Sr/86Sr variability at JAR, however, is positively correlated with the δ18O record. Preliminary 87Sr/86Sr results from PAR are only broadly consistent with

An Experimental Study on What Controls the Ratios of 18O/16O and 17O/16O of O2 During Microbial Respiration

Science.gov (United States)

Stolper, D. A.; Ward, B. B.; Fischer, W. W.; Bender, M. L.

2015-12-01

18O/16O and 17O/16O ratios of atmospheric and dissolved oceanic O2 are key biogeochemical tracers of total photosynthesis and respiration on global to local length scales and glacial/interglacial time scales (Luz et al., 1999). Critical to the use of these ratios as biogeochemical tracers is knowledge of how they are affected by production, consumption, and transport of O2. We present new measurements of O2 respiration by E. coli and N. oceanus, an ammonia oxidizing bacterium, to test three assumptions of isotopically enabled models of the O2 cycle: (i) laboratory-measured respiratory 18O/16O isotope effects (18α) of microorganisms are constant under all experimental and natural conditions (e.g., temperature and growth rate); (ii) the respiratory 'mass law' relationship between 18O/16O and 17O/16O [17α = (18α)β] is universal; and (iii) 18α and β for aerobic ammonia and organic carbon oxidation are identical. For E. coli, we find that both 18α and β are variable. From 37°C to 15°C, 18α varies linearly with temperature from 17 to 14‰, and β varies linearly from 0.513 to 0.508. 18α and β do not appear to vary with growth rate (as tested using different carbon sources). Both 18α and β are lower than previous observations for bacteria: 18α = 17-20‰ (Kiddon et al., 1993) and β = 0.515 (Luz and Barkan, 2005). We were able to simulate the observed temperature dependence of 18α and β using a model of respiration with two isotopically discriminating steps: O2 binding to cytochrome bo oxidase (the respiratory enzyme) and reduction of O2 to H2O. Finally, initial results on N. oceanus suggest it has similar values for 18α and β as previously studied aerobic bacteria that consume organic carbon, providing the first support for assumption (iii). Based on these results, isotopically constrained biogeochemical models of O2 cycling may need to consider a temperature dependence for 18α and β for microbial respiration. For example, these results may

Geochemistry of the stable isotopes of silicon

Energy Technology Data Exchange (ETDEWEB)

Douthitt, C B [California Inst. of Tech., Pasadena (USA). Div. of Geological and Planetary Sciences

1982-08-01

One hundred thirty two new measurements of the relative abundances of the stable isotopes of silicon in terrestrial materials are presented. The total variation of delta/sup 30/Si found is 6.2 parts per thousand, centered on the mean of terrestrial mafic and ultramafic igneous rocks, delta/sup 30/Si = -0.4 parts per thousand. Igneous rocks show limited variation; coexisting minerals exhibit small, systematic silicon isotopic fractionations that are roughly 1/3 the magnitude of concomitant oxygen isotopic fractionations at 1150/sup 0/C. In both igneous minerals and rocks, delta/sup 30/Si shows a positive correlation with silicon content, as does delta/sup 18/O. Opal from both sponge spicules and sinters is light, with delta/sup 30/Si = -2.3 and -1.4 parts per thousand respectively. Large delta/sup 30/Si values of both positive and negative sign are reported for the first time from clay minerals, opaline phytoliths, and authigenic quartz. All highly fractionated samples were precipitated from solution at low temperatures; however, aqueous silicon is not measurably fractionated relative to quartz at equilibrium. A kinetic isotope fractionation of approximately 3.5 parts per thousand is postulated to occur during the low temperature precipitation of opal and, possibly, poorly ordered phyllosilicates, with the silicate phase being enriched in /sup 28/Si. This fractionation, coupled with a Rayleigh precipitation model, is capable of explaining most non-magmatic delta/sup 30/Si variations.

Isotopic geochronology of granitic rocks from the Central Iberian Zone: comparison of methodologies

Energy Technology Data Exchange (ETDEWEB)

Antunes, I. M. H. R.; Neiva, A. M. R.; Silva, M. M. V. G.

2010-07-01

Five granitic rocks, concentrically disposed from core to rim, were distinguished in the Castelo Branco pluton. U-Pb-Th electron microprobe monazite ages from granitic rocks are similar and ranging between 297-303 Ma. The granitic rocks from Castelo Branco pluton are 310 {+-} 1 Ma old, obtained by U-Pb (ID-TIMS) in separated zircon and monazite crystals, indicating a similar emplacement age for all granitic rocks of the pluton. Initial {sup 8}7Sr/{sup 8}6Sr isotopic ratios and {epsilon}Nd{sub 3}10 and {delta}{sup 1}8O values suggest three distinct pulses of granitic magma and that they are derived from partial melting of heterogeneous metasedimentary materials. The other granitic rocks are related by magmatic differentiation and show small variations in ({sup 8}7Sr/{sup 8}6Sr)310, {epsilon}Nd{sub 3}10 and {delta}{sup 1}8O. The granitic pluton of Castelo Branco shows a rare reverse zoning. (Author) 12 refs.

Water isotopic characterization of hypersaline formation of a petroleum field Reconcavo basin, Brazil; Caracterizacao isotopica de aguas de formacao hipersalinas de um campo de petroleo da Bacia do Reconcavo, Brasil

Energy Technology Data Exchange (ETDEWEB)

Teles, Danilo Ribeiro de Sa; Azevedo, Antonio Expedito Gomes de, E-mail: danilosateles@yahoo.com.br, E-mail: expedito@ufba.br [Universidade Federal da Bahia (UFBA), Salvador, BA (Brazil). Inst. de Fisica. Centro de Pesquisa em Geofisica e Geologia; Santos, Christian Pereira Lopes dos, E-mail: cplsgs@gmail.com [Instituto Federal Baiano, Salvador, BA (Brazil)

2010-04-15

Formation water is the water present in reservoir rock pores, produced together with petroleum. Usually it is hyper saline with concentrations that can be higher than 250 g/l of dissolved solids. The concentration of the dissolved elements and the isotopic composition of the water and of some of the dissolved elements can be excellent tracers to study the dynamic of underground fluid flux, the mixing of distinct sources and the origin of salinization of these waters. This work reports the isotopic composition ({delta}{sup 2}H , {delta}{sup 18}O) and electrical conductivity (EC) of formation waters from 10 wells of a petroleum field of the Reconcavo Basin, looking for their evolution, interaction with the minerals and rocks and reservoir interconnection. The samples have electric conductivity ranging from 84 to 137 mS/cm, with conductivity increasing with depth of production zone. It is observed an enrichment of deuterium and oxygen-18 with the depth of production zone, probably due to water-rock interactions that were probably increased by higher temperatures of the deeper levels and longer residence times. The samples from the production zone between 1450 to 1520 m, drained by 7 of the 10 wells sampled, show a small range in isotopic composition and in electric conductivity, indicating homogeneity in this level of the reservoir. In the shallow level of 450 m the values of {delta}{sup 2}H , {delta}{sup 18}O and EC are lower, with isotopic composition similar to the oceanic water, possibly representing the original water that entered the reservoir during the sedimentation of the basin. (author)

Estimated values of the environmental tritium concentration and the altitude isotope effects of δD and δ18O in Hokkaido

International Nuclear Information System (INIS)

Ikeda, Mitsuyoshi; Takata, Sigeru; Matsueda, Hiroharu

1998-01-01

Tritium ( 3 H) concentration and stable isotopic ratios δD and δ 18 O are important environmental tracer data. In Hokkaido, however, hydrological studies using these data were difficult due to a lack of environmental tritium and the altitude isotope effect values. In this study, 3 H concentrations of Hokkaido wine were measured to estimate the past rain 3 H concentrations. In addition, environmental δD and δ 18 O samples taken on Mt. Daisetsuzan, the highest peak in Hokkaido, and in the Tokachi Plain were measured. The results obtained are as follows: Estimated concentrations of 3 H in Hokkaido were higher than those in Tokyo and Tsukuba, and were consistent with geographical 3 H levels in rain around Hokkaido. Some model calculations suggested that the 3 H concentrations in the 1950's and 1960's were at least 30% higher than those in Tokyo. The altitude isotope effects obtained were -1.75±0.30 per mille/100 m and -0.24±0.01 per mille/100 m for δD and δ 18 O, respectively. These values are almost the same as, or slightly lower than those in the Chubu and Tohoku districts. Using these data, the approximate age of groundwater and the altitude of original precipitation could be estimated. (author)

Unraveling climatic changes from intraprofile variation in oxygen and hydrogen isotopic composition of goethite and kaolinite in laterites: An integrated study from Yaou, French Guiana

Energy Technology Data Exchange (ETDEWEB)

Girard, J.P.; Freyssinet, P.; Chazot, G.

2000-02-01

An integrated study of O and H isotopes in the latertic profile of Yaou, French Guiana, was undertaken to investigate the usefulness of stable isotopes as tracers of climatic changes in continental environments. The studied profile is composed of a 27 m thick saprolite, mostly developed in the past under wet-and-dry tropical climate in association with a duricrust, overlain by a 3 m thick yellow latosol formed more recently under present equatorial hot and humid climate. {delta}{sup 18}O-{delta}D values determined for weathering goethite (pseudomorphs after pyrite) and kaolinite (microcrystalline clay groundmass) throughout the 30 m deep profile reflect formation temperatures consistent with present (25 C) and realistic past climatic temperatures (20 C--30 C), indicating that weathering minerals formed in isotopic equilibrium with their genetic environment and were not subjected to significant isotope exchange after formation. A distinct shift downward from low to high {delta}{sup 18}O-{delta}D values occurs around 20 m depth in the saprolite. It is interpreted as recording the change from the past tropical to the present equatorial climate. Goethite and kaolinite in the 5--10 m thick saprolite interval immediately above the active basement weathering front are in isotopic equilibrium with modern water and must have formed under present equatorial-humid conditions. In contrast, goethite and kaolinite found higher up on the saprolite and in the duricrust formed in the past under tropical wet and dry climate from waters distinctly depleted in {sup 18}O and D relative to modern water. The marked depletion of paleo-meteoric water at Yaou most likely reflects a more contrasted or monsoonal character of the ancient tropical climate. The present study shows that ancient weathering minerals in lateritic profiles preserve their {delta}{sup 18}O-{delta}D values and carry a time signal. The time signal is best expressed in minerals formed rapidly at the weathering front and

Isotopic Assessment of Nitrogen Cycling in River Basins: Potential and Limitations for Nutrient Management Purposes

Energy Technology Data Exchange (ETDEWEB)

Mayer, B. [Department of Geoscience, University of Calgary, Calgary, Alberta (Canada); Sebilo, M. [PMC University Paris 06, UMR BIOEMCO, Paris (France); Wassenaar, L. I. [Environment Canada, Saskatoon (Canada)

2013-05-15

It has been proposed that the stable isotopic composition of riverine nitrate may help reveal the predominant sources of N loading of riverine systems, including inorganic fertilizers and manure derived nitrates from agricultural systems and nitrates from urban wastewater effluents. A literature review reveals that rivers in pristine and forested headwaters are generally characterized by low nitrate concentrations and {delta}{sup 15}N{sub nitrate} values <5 per mille, whereas rivers draining well developed watersheds characterized by major urban centres and/or intensive agriculture have higher nitrate concentrations and {delta}{sup 15}N{sub nitrate} values of between +5 and +15% per mille. Relating elevated {delta}{sup 15}N{sub nitrate} values to specific nitrogen sources or to estimate nutrient loading rates for management purposes, however, is challenging for a variety of reasons: (1) the nitrogen isotopic composition of agricultural derived nitrate can be variable and may overlap with the {delta}{sup 15}N value of wastewater nitrate; (2) soil zone and riparian denitrification may cause changes in the concentration and isotopic composition of riverine nitrate; and (3) in-stream nutrient uptake processes may affect the isotopic composition of dissolved nitrogen compounds. To maximize the information gained from isotopic studies of riverine nitrogen compounds we recommend that: (1) numerous sampling sites are established along a river and sampled frequently in order to capture spatial and seasonal changes; (2) the isotopic composition of nitrate (including {sup 18}O/{sup 16}O) and dissolved ammonium be determined if possible; (3) riverine nitrogen loading be determined and interpreted in context along with isotope data, and; (4) major and relevant nitrogen inputs to the watershed be identified and their isotopic values measured. This approach will help to minimize ambiguities in the interpretation of obtained isotope data and maximize the information required for

Using Whole Stream {delta}{sup 15}N Additions to Understand the Effects of Land Use Change on Stream Function

Energy Technology Data Exchange (ETDEWEB)

Deegan, L. A.; Neill, C.; Thomas, S.; Haupert, C. [Marine Biological Laboratory, Woods Hole, MA (United States); Victoria, R. L.; Krusche, A. V.; Ballester, M. V.R. [Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Sao Paulo (Brazil)

2013-05-15

In this paper we introduce an emerging new technique; the use of {delta}{sup 15}N stable isotope tracers to understand both short term and long term alterations in stream ecosystem nitrogen biogeochemistry and food web dynamics. The use of {delta}{sup 15}N isotopes to determine stream nitrogen cycling was developed in small tundra streams in Alaska (USA), but a network of researchers using similar technique has rapidly grown to answer questions about nitrogen cycling and stream food webs in a variety of ecosystem types and subject to human modifications. Here we provide an overview of some of the information that can be provided using stable isotope additions and describe the general approach of an isotope addition experiment. To illustrate the scope of isotope applicability some examples are provided of work undertaken in the Brazilian Amazon. (author)

Natural Tracers and Isotope Techniques to Define Groundwater Recharge and Salinization in the Bou Areg Coastal Aquifer (North Morocco)

Energy Technology Data Exchange (ETDEWEB)

Re, V. [Department of Molecular Sciences and Nanosystems, University Ca' Foscari, Venice (Italy); Allais, E. [ISO4 s.n.c., Torino (Italy); El Hamouti, N. [Multidisciplinary Faculty of Nador, University of Oujda, Nador (Morocco); Bouchnan, R. [Laboratory of Physical Phenomena and Natural Risk Modelling, University of Tangier, Tangier (Morocco); Sacchi, E. [Department of Earth Sciences, University of Pavia, Pavia (Italy); Rizzo, F. [UNESCO International Hydrological Programme, Paris (France); Zuppi, G. M. [Department of Molecular Sciences and Nanosystems, University Ca' Foscari, Venice and Institute of Environmental Geology and Geoengineering, National Research Council, Monterotondo (Italy)

2013-07-15

The geochemical and isotopic ({delta}{sup 2}H, {delta}{sup 18}O, {delta}{sup 13}C, {delta}{sup 15}N{sub NO3},{delta} {sup 18}O{sub NO3}) characterization of the Bou Areg aquifer (North Morocco) based on samples collected during two surveys in November 2009 and June 2010 allowed the identification of run-off from the mountain regions and agricultural return flows as the main sources of aquifer recharge. The high salinization of the aquifer is not only due to the intensive agricultural activities but it is also associated with the natural quality of the catchment. The isotopic signal of dissolved nitrates allowed for the identification of two main sources of nitrogen in the system: (i) fertilizers and (ii) manure and septic effluents. The study, framed within the UNESCO-IHP sub component of the Strategic Partnership for the Mediterranean Large Marine Ecosystem, represents the first isotopic investigation of the area and will serve as a basis for the promotion of robust science based management practices in the region. (author)

Toward a Mechanistic Understanding of Deuterium Excess as a Tracer for Evapotranspiration

Energy Technology Data Exchange (ETDEWEB)

Lai, Chun-Ta [Department of Biology, San Diego State University, San Diego, CA (United States)

2013-07-15

An understanding of atmospheric water vapour and its isotopic composition is useful for modelling effects of terrestrial evapotranspiration on regional hydrologic cycles. Previous studies showed diurnal and vertical patterns of water vapour isotope ratios ({delta}{sup 2}H{sub v} and {delta}{sup 18}O{sub v}) consistently observed in an old growth coniferous forest. Using a box model and a mass balance approach to simulate 'isoflux of d-excess', the effect of evapotranspiration on the d-excess in atmospheric water vapour is quantitatively demonstrated. The results suggest that d-excess can be mechanistically utilized to identify processes that contribute to the diurnal variation in atmospheric moisture. These new findings have implications for larger-scale predictions of precipitation across the terrestrial landscape. In this paper, I report the initial results of the {delta}{sup 2}H{sub v} and {delta}{sup 18}O{sub v} measurements using a cavity enhanced spectroscopy instrument. These recent data are consistent with the pattern observed by the conventional sampling method, providing new opportunities for studying d-excess as a tracer for evapotranspiration. (author)

Use of Isotopic Techniques for the Assessment of Hydrological Processes in Wetlands (Cienaga Colombia)

Energy Technology Data Exchange (ETDEWEB)

Betancur, T.; Santa, D.; Palacio, P.; Palacio, C.; Wills, B.; Hoyos, D. A. [Universidad de Antioquia, Medellin (Colombia)

2013-07-15

The Cienaga Colombia wetland is located in the Bajo Cauca Antioqueno region where the 'Man' river flows into the Cauca River. Hydrological processes on the Cienaga Colombia wetland are complex because of the interactive effects of both local and regional elements, associated with a typical tropical wet climatic regime. In this groundwater dependent wetland hydrological studies have been conducted, including hydrochemical analyses and isotope tracers, to describe and understand the interactions between groundwater and surface water, not only for the wetland itself but also for the entire catchment area. Rain samples (five year record) were used to obtain the LML: {delta}{sup 2}H = 8.03 {delta}{sup 18}O +9.9. The evaporation line is: {delta}{sup 2}H = 5.9 {delta}{sup 18}O - 7.3. According to the analyses, both groundwater and surface waters have the same isotopic signatures. Unsustainable land use practices along with current and predicted global environmental changes may cause negative impacts on the hydrological functioning of the region, affecting primarily, but not exclusively, evapotranspiration-recharge processes and the sustainability of the entire system. (author)

Investigation of isotopes and hydrological processes in Indus river system, Pakistan

International Nuclear Information System (INIS)

Manzoor Ahmad, M; Latif, Z.; Tariq, J.A.; Akram, W.; Rafique, M.

2009-11-01

dominance of moisture source from Mediterranean. Kachura station having delta /sup 18/O- /sup 2/H line with slope 4 and low d-excess shows evaporation effect in Kachura Lake. Delta /sup 18/O and delta /sup 2/H values of Indus River get enriched going downstream towards Arabian Sea because of contribution from rains at low altitude plains and base flow, and evaporation. Low tritium in some samples also indicates contribution of base flow (relatively older groundwater). River Chenab has the widest variation in delta /sup 18/O and delta /sup 2/H, and slope of delta/sup 18/O- delta/sup 2/H line is 6.1, which is due to variable contribution of snow melt at high altitude and rains fallen at low altitudes. High d-excess in snow melt and low d-excess in monsoon show that the moisture source in winter is generally western (Mediterranean) and the monsoon dominantly originates from Indian Ocean. The isotope data also reflect evaporation effect during dry periods. Kabul River has wide variation in isotopic values due to variable contribution from Swat River, which carries snow melt. High d-excess is associated with the depleted isotopic values, while low d-excess is associated with enriched isotopic values generally during summer monsoon. Therefore, slope of delta/sup 18/O- delta/sup 2/H line is 7, which seems mainly due to dominance of moisture source from Mediterranean in winter (having depleted isotopic values and high d-excess) and from Bay of Bengal in summer with relatively high d-excess. River Jhelum and its tributaries upstream of Mangla Lake have enriched delta /sup 18/O and delta /sup 2/H due to low altitude of its catchment. The precipitation in the catchment of river Ravi results from the moisture source from Indian Ocean and there is not any significant effect of evaporation. The isotopic variation seems mainly due to water diversions from the western rivers through link canals. (author)

Simulating dynamics of {delta}{sup 13}C of CO{sub 2} in the planetary boundary layer a boreal forest region: covariation between surface fluxes and atmospheric mixing

Energy Technology Data Exchange (ETDEWEB)

Chen, Baozhang; Chen, Jing M. [Univ. of Toronto, ON (Canada). Dept. of Geography; Tans, Pieter P. [National Oceanic and Atmospheric Administration, Boulder, CO (United States). Earth System Research Lab.; Huang, Lin [Environment Canada, Toronto, ON (Canada). Atmospheric Science and Technology Directorate

2006-11-15

Stable isotopes of CO{sub 2} contain unique information on the biological and physical processes that exchange CO{sub 2} between terrestrial ecosystems and the atmosphere. Ecosystem exchange of carbon isotopes with the atmosphere is correlated diurnally and seasonally with the planetary boundary layer (PBL) dynamics. The strength of this kind of covariation affects the vertical gradient of {delta}{sup 13}C and thus the global {delta}{sup 13}C distribution pattern. We need to understand the various processes involved in transport/diffusion of carbon isotope ratio in the PBL and between the PBL and the biosphere and the troposphere. In this study, we employ a one-dimensional vertical diffusion/transport atmospheric model (VDS), coupled to an ecosystem isotope model (BEPS-EASS) to simulate dynamics of {sup 13}CO{sub 2} in the PBL over a boreal forest region in the vicinity of the Fraserdale (FRD) tower (49 deg 52 min 29.9 sec N, 81 deg 34 min 12.3 sec W) in northern Ontario, Canada. The data from intensive campaigns during the growing season in 1999 at this site are used for model validation in the surface layer. The model performance, overall, is satisfactory in simulating the measured data over the whole course of the growing season. We examine the interaction of the biosphere and the atmosphere through the PBL with respect to {delta}{sup 13}C on diurnal and seasonal scales. The simulated annual mean vertical gradient of {delta}{sup 13}C in the PBL in the vicinity of the FRD tower was about 0.025% in 1999. The {delta}{sup 13}C vertical gradient exhibited strong diurnal (29%) and seasonal (71%) variations that do not exactly mimic those of CO{sub 2}. Most of the vertical gradient (96.5% {+-}) resulted from covariation between ecosystem exchange of carbon isotopes and the PBL dynamics, while the rest (3.5%{+-}) was contributed by isotopic disequilibrium between respiration and photosynthesis. This disequilibrium effect on {delta}{sup 13}C of CO{sub 2} dynamics in PBL

Simulating dynamics of (delta){sup 13}C of CO{sub 2} in the planetary boundary layer a boreal forest region: covariation between surface fluxes and atmospheric mixing

Energy Technology Data Exchange (ETDEWEB)

Chen, Baozhang; Chen, Jing M. [Univ. of Toronto, ON (Canada). Dept. of Geography; Tans, Pieter P. [National Oceanic and Atmospheric Administration, Boulder, CO (United States). Earth System Research Lab.; Huang, Lin [Environment Canada, Toronto, ON (Canada). Atmospheric Science and Technology Directorate

2006-11-15

Stable isotopes of CO{sub 2} contain unique information on the biological and physical processes that exchange CO{sub 2} between terrestrial ecosystems and the atmosphere. Ecosystem exchange of carbon isotopes with the atmosphere is correlated diurnally and seasonally with the planetary boundary layer (PBL) dynamics. The strength of this kind of covariation affects the vertical gradient of (delta){sup 13}C and thus the global (delta){sup 13}C distribution pattern. We need to understand the various processes involved in transport/diffusion of carbon isotope ratio in the PBL and between the PBL and the biosphere and the troposphere. In this study, we employ a one-dimensional vertical diffusion/transport atmospheric model (VDS), coupled to an ecosystem isotope model (BEPS-EASS) to simulate dynamics of {sup 13}CO{sub 2} in the PBL over a boreal forest region in the vicinity of the Fraserdale (FRD) tower (49 deg 52 min 29.9 sec N, 81 deg 34 min 12.3 sec W) in northern Ontario, Canada. The data from intensive campaigns during the growing season in 1999 at this site are used for model validation in the surface layer. The model performance, overall, is satisfactory in simulating the measured data over the whole course of the growing season. We examine the interaction of the biosphere and the atmosphere through the PBL with respect to (delta){sup 13}C on diurnal and seasonal scales. The simulated annual mean vertical gradient of (delta){sup 13}C in the PBL in the vicinity of the FRD tower was about 0.025% in 1999. The (delta){sup 13}C vertical gradient exhibited strong diurnal (29%) and seasonal (71%) variations that do not exactly mimic those of CO{sub 2}. Most of the vertical gradient (96.5% {+-}) resulted from covariation between ecosystem exchange of carbon isotopes and the PBL dynamics, while the rest (3.5%{+-}) was contributed by isotopic disequilibrium between respiration and photosynthesis. This disequilibrium effect on (delta){sup 13}C of CO{sub 2} dynamics in PBL

Tritium in [18O]water containing [18F]fluoride for [18F]FDG synthesis

International Nuclear Information System (INIS)

Ito, Shigeki; Saze, Takuya; Sakane, Hitoshi; Ito, Satoshi; Ito, Shinichi; Nishizawa, Kunihide

2004-01-01

The presence of tritium in enriched [ 18 O]water irradiated with 9.6 MeV protons used to produce [ 18 F]fluoride by the 18 O(p, n) 18 F reaction was inferred from the cross sections and threshold energies of the 18 O(p, t) 16 O reaction, and the existence of tritium was confirmed experimentally. Tritium was also detected in both [ 18 O]water recovered for recycling and waste acetonitrile solutions. The purified [ 18 F]FDG was not contaminated with 3 H. The amount of 3 H discharged into the air was far less than the International Basic Safety Standard Level

Impact of carbohydrate supply on stem growth, wood and respired CO{sub 2} {delta}{sup 13}C : assessment by experimental girdling

Energy Technology Data Exchange (ETDEWEB)

Maunoury-Danger, F. [Paris-Sud Univ., Orsay Cedex (France). Laboratoire Ecologie, Systematique et Evolution; Centre National de la Recherche Scientifique, Orsay CEDEX (France); AgroParisTech, Paris (France); Paul Verlaine-Metz Univ., Metz (France). Laboratoire des Interactions Ecotoxicologie Biodiversite Ecosystemes; Fresneau, C.; Eglin, T.; Berveiller, D.; Francois, C.; Damesin, C. [Paris-Sud Univ., Orsay Cedex (France). Laboratoire Ecologie, Systematique et Evolution; Centre National de la Recherche Scientifique, Orsay CEDEX (France); AgroParisTech, Paris (France); Lelarge-Trouverie, C. [Paris-Sud Univ., Orsay Cedex (France). Inst. de Biotechnologie des Plantes, Plateforme Metabolisme-Metabolome

2010-07-15

In trees, carbohydrate storage and remobilization may affect the carbon isotope signals of sugars exported from leaves, tree organic matter and respired carbon dioxide (CO{sub 2}). This study characterized the impact of a change in the carbon (C) source used for stem functioning on the {delta}{sup 13} C of stem organic matter and respired CO{sub 2}. Girdling experiments were carried out on 2-year old oaks that consisted in removing the bark and phloem around the stem so that the sap would cease to flow. The stem was therefore forced to use its own C reserves to maintain metabolic activity. Trees were girdled at 3 different periods, notably just after budburst, during stem growth, and just after cessation of stem radial growth. Stem radial growth and respiration rate were measured throughout the year. Other measured variables included {delta}{sup 13} C of respired CO{sub 2} and contents of starch and water-soluble fraction in stems and leaves. The study showed that girdling stopped growth, even early in the growing season, leading to a decrease in stem CO{sub 2} efflux. The study demonstrated that leaf carbohydrate supply versus reserve use could be an important factor controlling stem growth and {delta}{sup 13} C of both ring and stem CO{sub 2} efflux. 69 refs., 3 tabs., 5 figs.

Chemistry of fluids from a natural analogue for a geological CO{sub 2} storage site (Montmiral, France): Lessons for CO{sub 2}-water-rock interaction assessment and monitoring

Energy Technology Data Exchange (ETDEWEB)

Pauwels, Helene [BRGM - Water Division, 3, av Claude Guillemin, 45060 Orleans Cedex (France)], E-mail: h.pauwels@brgm.fr; Gaus, Irina; Le Nindre, Yves Michel [BRGM - Water Division, 3, av Claude Guillemin, 45060 Orleans Cedex (France); Pearce, Jonathan [British Geological Survey, Kingsley Dunham Centre, Keyworth, Nottingham NG125GG (United Kingdom); Czernichowski-Lauriol, Isabelle [BRGM - Water Division, 3, av Claude Guillemin, 45060 Orleans Cedex (France)

2007-12-15

Chemical and isotope studies of natural CO{sub 2} accumulations aid in assessing the chemical effects of CO{sub 2} on rock and thus provide a potential for understanding the long-term geochemical processes involved in CO{sub 2} geological storage. Several natural CO{sub 2} accumulations were discovered during gas and oil exploration in France's carbogaseous peri-Alpine province (south-eastern France) in the 1960s. One of these, the Montmiral accumulation at a depth of more than 2400 m, is currently being exploited. The chemical composition of the water collected at the wellhead has changed in time and the final salinity exceeds 75 g/L. These changes in time can be explained by assuming that the fraction of the reservoir brine in the recovered brine-CO{sub 2}-H{sub 2}O mixture varies, resulting in variable proportions of H{sub 2}O and brine in the sampled water. The proportions can be estimated in selected samples due to the availability of gas and water flowrate data. These data enabled the reconstruction of the chemical and isotope composition of the brine. The proportions of H{sub 2}O and brine can also be estimated from isotope ({delta}{sup 2}H, {delta}{sup 18}O) composition of collected water and {delta}{sup 18}O of the sulfates or CO{sub 2}. The reconstituted brine has a salinity of more than 85 g/L and, according to its Br{sup -} content and isotope ({delta}{sup 2}H, {delta}{sup 18}O, {delta}{sup 34}S) composition, originates from an evaporated Triassic seawater that underwent dilution by meteoric water. The reconstitution of the brine's chemical composition enabled an evaluation of the CO{sub 2}-water-rock interactions based on: (1) mineral saturation indices; and (2) comparison with initial evaporated Triassic seawater. Dissolution of K- and SO{sub 4}-containing minerals such as K-feldspar and anhydrite, and precipitation of Ca and Mg containing minerals that are able to trap CO{sub 2} (carbonates) are highlighted. The changes in concentration of

Hydro-geochemical and isotopic fluid evolution of the Los Azufres geothermal field, Central Mexico

Energy Technology Data Exchange (ETDEWEB)

Gonzalez-Partida, E. [Centro de Geociencias, UNAM, Campus Juriquilla, A.P. 15, Juriquilla, Qro., 76230 (Mexico)]. E-mail: egp@geociencias.unam.mx; Carrillo-Chavez, A. [Centro de Geociencias, UNAM, Campus Juriquilla, A.P. 15, Juriquilla, Qro., 76230 (Mexico); Levresse, G. [Centro de Geociencias, UNAM, Campus Juriquilla, A.P. 15, Juriquilla, Qro., 76230 (Mexico); Tello-Hinojosa, E. [Comision Federal de Electricidad, A.P. 31-7, C.P. 58090 Morelia, Mich. (Mexico); Venegas-Salgado, S. [Comision Federal de Electricidad, A.P. 31-7, C.P. 58090 Morelia, Mich. (Mexico); Ramirez-Silva, G. [Comision Federal de Electricidad, A.P. 31-7, C.P. 58090 Morelia, Mich. (Mexico); Pal-Verma, M. [Instituto de Investigaciones Electricas, A.P. 1-475, C.P. 62001 Cuernavaca, Morelos (Mexico); Tritlla, J. [Centro de Geociencias, UNAM, Campus Juriquilla, A.P. 15, Juriquilla, Qro., 76230 (Mexico); Camprubi, A. [Centro de Geociencias, UNAM, Campus Juriquilla, A.P. 15, Juriquilla, Qro., 76230 (Mexico)

2005-01-01

minor magmatic component. The enrichment in {delta}{sup 18}O is due to the rock-water interaction at relatively high temperatures. {delta}{sup 13}C stable isotope data show a magmatic source with a minor meteoric contribution for CO{sub 2}. The initial isotopic value {delta}{sup 34}S{sub RES} = -2.3 per mille, which implies a magmatic source. More negative values are observed for shallow pyrite and range from {delta}{sup 34}S (FeS{sub 2}) = -4 per mille to -4.9 per mille, indicating boiling. The same fractionation tendencies are observed for fluids in the reservoir from results for {delta}{sup 18}O.

Processes affecting δ34S and δ18O values of dissolved sulfate in alluvium along the Canadian River, central Oklahoma, USA

Science.gov (United States)

Tuttle, Michele L.W.; Breit, George N.; Cozzarelli, Isabelle M.

2009-01-01

The δ34S and δ18O values for dissolved sulfate in groundwater are commonly used in aquifer studies to identify sulfate reservoirs and describe biogeochemical processes. The utility of these data, however, often is compromised by mixing of sulfate sources within reservoirs and isotope fractionation during sulfur redox cycling. Our study shows that, after all potential sulfate sources are identified and isotopically characterized, the δ34SSO4 and δ18OSO4 values differentiate processes such as sulfate-source mixing, sulfide oxidation, barite dissolution, and organosulfur decomposition. During bacterial reduction of sulfate, the values reflect kinetic sulfur isotope fractionation and exchange of oxygen isotopes between sulfate and water. Detailed analysis of the chemistry (Cl and SO4 concentrations) and isotopic composition (δ2HH2Oand δ18OH2O) of groundwater in an alluvial aquifer in Central Oklahoma, USA allowed the identification of five distinct end members that supply water to the aquifer (regional groundwater flowing into the study area, river water, leachate from a closed landfill that operated within the site, rain, and surface runoff). The δ34SSO4 and δ18OSO4 values in each end member differentiated three sources of sulfate: sulfate dissolved from Early to Late Permian rocks within the drainage basin (δ34SSO4 = 8–12‰ and δ18OSO4 = 10‰), iron sulfides oxidized by molecular oxygen during low water-table levels (δ34SSO4 = − 16‰ and δ18OSO4 = 10‰), and organosulfur compounds (predominately ester sulfates) from decomposition of vegetation on the surface and from landfill trash buried in the alluvium (δ34SSO4 = 8‰ and δ18OSO4 = 6‰). During bacterial reduction of these sulfate sources, similar isotope fractionation processes are recorded in the parallel trends of increasing δ34SSO4 and δ18OSO4 values. When extensive reduction occurs, the kinetic sulfur isotope fractionation (estimated by εH2S–SO4 = − 23�

Influence of Plio-Pleistocene basin hydrology on the Turkana hominin enamel carbonate δ(18)O values.

Science.gov (United States)

Quinn, Rhonda L

2015-09-01

Stable oxygen isotopes of hominin enamel carbonate (δ(18)OEC) provide a window into aspects of past drinking behavior and diet, body size, breastfeeding and weaning, mobility, and paleoclimate. It is tempting to compare all hominins across time and space in order to gauge species-level adaptations to changing environments and niche separation between those living sympatrically. Basinal, sub-basinal, and micro-environmental differences, however, may exert an influence on variation in enamel carbonate isotopic values that must be reconciled before hominin species across Africa can be meaningfully compared. Plio-Pleistocene Turkana hominin δ(18)OEC values show a considerable spread, potentially revealing many intrinsic and extrinsic contributing factors operating on different scales. In this study, I examine Turkana hominin δ(18)OEC values relative to identity (taxon, tooth type and number, body size of taxon), dietary (δ(13)C value, Turkana coeval and modern mammalian δ(18)OEC values), and contextual (time, depositional environment) information of each specimen and collection locality and discuss various potential influences. Turkana hominin δ(18)OEC values may primarily reflect differences in imbibed water sources (lake vs. river) as a function of evolving basin hydrology. Copyright © 2015 Elsevier Ltd. All rights reserved.

Thermonuclear reaction rate of 17O(p,γ)18F

International Nuclear Information System (INIS)

Fox, C.; Iliadis, C.; Champagne, A.E.; Fitzgerald, R.P.; Longland, R.; Newton, J.; Pollanen, J.; Runkle, R.

2005-01-01

The 17 O(p,γ) 18 F and 17 O(p,α) 14 N reactions have a profound influence on hydrogen-burning nucleosynthesis in a number of stellar sites, including red giants, asymptotic giant branch (AGB) stars, massive stars, and classical novae. Previously evaluated thermonuclear rates for both reactions carry large uncertainties. We investigated the proton-capture reaction on 17 O in the bombarding energy range of E p lab = 180-540 keV. We observed a previously undiscovered resonance at E R lab = 193.2 ± 0.9 keV. The resonance strength amounts to (ωγ) pγ (1.2±0.2)x10 -6 eV. With this value, the uncertainties of the 17 O(p,γ) 18 F reaction rates are reduced by orders of magnitude in the peak temperature range of classical novae (T=0.1-0.4 GK). We also report on a reevaluation of the 17 O(p,γ) 18 F reaction rates at lower temperatures that are pertinent to red giants, AGB stars, or massive stars. The present work establishes the 17 O(p,γ) 18 F reaction rates over a temperature range of T= 0.01-1.5 GK with statistical uncertainties of 10-50%. The new recommended reaction rates deviate from the previously accepted values by an order of magnitude around T≅0.2 GK and by factors of 2-3 at T < 0.1 GK

Seasonal Variations in Stable Isotope Ratios of Oxygen and Hydrogen in Two Tundra Rivers in NE European Russia

Energy Technology Data Exchange (ETDEWEB)

Huitu, E.; Arvola, L. [Lammi Biological Station, University of Helsinki (Finland); Sonninen, E. [Radiocarbon Dating Laboratory, University of Helsinki (Finland)

2013-07-15

The variability in stable isotope ratios of oxygen and hydrogen ({delta} {sup 18}O and {delta}{sup 2}H values) in river waters in northeast European Russia was studied for the period from July 2007 to october 2008. Exceptional isotope composition in precipitation obtained during the sampling period was clearly traced in the composition of river waters. Water from permafrost thawing did not make a great contribution to river flow. (author)

{delta}{sup 13}C of Tree-Ring Lignin as an Indirect Measure of Climate Change

Energy Technology Data Exchange (ETDEWEB)

Robertson, I. [CSIR Environmentek, Quaternary Dating Research Unit (South Africa)], E-mail: i.robertson@swansea.ac.uk; Loader, N. J.; McCarroll, D. [University of Wales Swansea, Department of Geography (United Kingdom); Carter, A. H. C. [University of Cambridge, Godwin Institute for Quaternary Research (United Kingdom); Cheng, L.; Leavitt, S. W. [University of Arizona, Laboratory of Tree-Ring Research (United States)

2004-06-15

High-resolution paleoclimatic data are an essential requirement for testing numerical models of climate change and the global carbon cycle. If the long tree-ring chronologies, originally established for the purpose of dendrochronology, are to be fully exploited as an indirect measure of past climatic variability, additional techniques are required to obtain this information. The determination of the {delta}{sup 13}C value of tree-ring cellulose has been used successfully to reconstruct past climates. However, under both aerobic and anaerobic conditions, the polysaccharide components of vascular plants (mainly cellulose and hemicelluloses) are more prone to rapid degradation than lignin. This has serious implications for the use of carbon isotope values of tree-ring cellulose as an indirect measure of past climates. An absolutely dated ring-width chronology was established for oaks (Quercus robur L.) growing at Sandringham Park in eastern England. Carbon isotope values were determined on {alpha}-cellulose and 'Klason' lignin isolated from annual latewood samples over the period AD 1895-1999. The carbon isotope values of earlywood lignin are correlated with the latewood carbon isotope values of the previous year, supporting the theory that some of the carbon utilised in earlywood synthesis is assimilated in the previous year. The high-frequency variance in the carbon isotope indices of latewood lignin and cellulose is highly correlated with combined July and August environmental variables, indicating that they were formed at similar times. There was no evidence of secondary lignification. These results demonstrate that the determination of carbon isotope values of latewood lignin offers the potential to obtain unambiguous proxy climatic data covering several millennia.

Gas Hydrate Occurrence Inferred from Dissolved Cl− Concentrations and δ18O Values of Pore Water and Dissolved Sulfate in the Shallow Sediments of the Pockmark Field in Southwestern Xisha Uplift, Northern South China Sea

Directory of Open Access Journals (Sweden)

Min Luo

2014-06-01

Full Text Available Deep-water pockmarks are frequently accompanied by the occurrence of massive gas hydrates in shallow sediments. A decline in pore-water Cl− concentration and rise in δ18O value provide compelling evidence for the gas hydrate dissociation. Mega-pockmarks are widely scattered in the southwestern Xisha Uplift, northern South China Sea (SCS. Pore water collected from a gravity-core inside of a mega-pockmark exhibits a downward Cl− concentration decrease concomitant with an increase in δ18O value at the interval of 5.7–6.7 mbsf. Concentrations of Cl−, Na+, and K+ mainly cluster along the seawater freshening line without distinct Na+ enrichment and K+ depletion. Thus, we infer that the pore water anomalies of Cl− concentrations and δ18O values are attributed to gas hydrate dissociation instead of clay mineral dehydration. Moreover, the lower δ18O values of sulfate in the target core (C14 than those in the reference core (C9 may be associated with the equilibrium oxygen fractionation during sulfate reduction between sulfate and the relatively 18O-depleted ambient water resulting from gas hydrate formation. The gas hydrate contents are estimated to be 6%–10% and 7%–15%, respectively, according to the offset of Cl− concentrations and δ18O values from the baselines. This pockmark field in southwestern Xisha Uplift is likely to be a good prospective area for the occurrence of gas hydrate in shallow sediments.

Effects of variation in background mixing ratios of N2, O2, and Ar on the measurement of δ18O–H2O and δ2H–H2O values by cavity ring-down spectroscopy

Directory of Open Access Journals (Sweden)

J. E. Johnson

2017-08-01

Full Text Available Cavity ring-down spectrometers have generally been designed to operate under conditions in which the background gas has a constant composition. However, there are a number of observational and experimental situations of interest in which the background gas has a variable composition. In this study, we examine the effect of background gas composition on a cavity ring-down spectrometer that measures δ18O–H2O and δ2H–H2O values based on the amplitude of water isotopologue absorption features around 7184 cm−1 (L2120-i, Picarro, Inc.. For background mixtures balanced with N2, the apparent δ18O values deviate from true values by −0.50 ± 0.001 ‰ O2 %−1 and −0.57 ± 0.001 ‰ Ar %−1, and apparent δ2H values deviate from true values by 0.26 ± 0.004 ‰ O2 %−1 and 0.42 ± 0.004 ‰ Ar  %−1. The artifacts are the result of broadening, narrowing, and shifting of both the target absorption lines and strong neighboring lines. While the background-induced isotopic artifacts can largely be corrected with simple empirical or semi-mechanistic models, neither type of model is capable of completely correcting the isotopic artifacts to within the inherent instrument precision. The development of strategies for dynamically detecting and accommodating background variation in N2, O2, and/or Ar would facilitate the application of cavity ring-down spectrometers to a new class of observations and experiments.

Depositional facies and aqueous-solid geochemistry of travertine-depositing hot springs (Angel Terrace, Mammoth Hot Springs, Yellowstone National Park, USA)

Energy Technology Data Exchange (ETDEWEB)

Fouke, B.W.; Farmer, J.D.; Des Marais, D.J.; Pratt, L.; Sturchio, N.C.; Burns, P.C.; Discipulo, M.K.

2000-05-01

Petrographic and geochemical analyses of travertine-depositing hot springs at Angel Terrace, Mammoth Hot Springs, Yellowstone National Park, have been used to define five depositional facies along the spring drainage system. Spring waters are expelled in the vent facies at 71 to 73 C and precipitate mounded travertine composed of aragonite needle botryoids. The apron and channel facies (43--72 C) is floored by hollow tubes composed of aragonite needle botryoids that encrust sulfide-oxidizing Aquificales bacteria. The travertine of the pond facies (30--62 C) varies in composition from aragonite needle shrubs formed at higher temperatures to ridged networks of calcite and aragonite at lower temperatures. Calcite ice sheets, calcified bubbles, and aggregates of aragonite needles (fuzzy dumbbells) precipitate at the air-water interface and settle to pond floors. The proximal-slope facies (28--54 C), which forms the margins of terracette pools, is composed of arcuate aragonite needle shrubs that create small microterracettes on the steep slope face. Finally, the distal-slope facies (28--30 C) is composed of calcite spherules and calcite feather crystals. Despite the presence of abundant microbial mat communities and their observed role in providing substrates for mineralization, the compositions of spring-water and travertine predominantly reflect abiotic physical and chemical processes. Vigorous CO{sub 2} degassing causes a +2 unit increase in spring water pH, as well as Rayleigh-type covariations between the concentration of dissolved inorganic carbon and corresponding {delta}{sup 13}C. Travertine {delta}{sup 13}C and {delta}{sup 18}O are nearly equivalent to aragonite and calcite equilibrium values calculated from spring water in the higher-temperature ({approximately}50--73 C) depositional facies. Conversely, travertine precipitating in the lower-temperature (<{approximately}50 C) depositional facies exhibits {delta}{sup 13}C and {delta}{sup 18}O values that are as

Holocene record of precipitation seasonality from lake calcite δ18O in the central Rocky Mountains, United States

Science.gov (United States)

Anderson, Lesleigh

2011-01-01

A context for recent hydroclimatic extremes and variability is provided by a ~10 k.y. sediment carbonate oxygen isotope (??18O) record at 5-100 yr resolution from Bison Lake, 3255 m above sea level, in northwestern Colorado (United States). Winter precipitation is the primary water source for the alpine headwater lake in the Upper Colorado River Basin and lake water ??18O measurements reflect seasonal variations in precipitation ??18O. Holocene lake water ??18O variations are inferred from endogenic sedimentary calcite ??18O based on comparisons with historic watershed discharge records and tree-ring reconstructions. Drought periods (i.e., drier winters and/or a more rain-dominated seasonal precipitation balance) generally correspond with higher calcite ??18O values, and vice-versa. Early to middle Holocene ??18O values are higher, implying a rain-dominated seasonal precipitation balance. Lower, more variable ??18O values after ca. 3500 yr ago indicate a snow-dominated but more seasonally variable precipitation balance. The middle to late Holocene ??18O record corresponds with records of El Ni??o Southern Oscillation intensification that supports a teleconnection between Rocky Mountain climate and North Pacific sea-surface temperatures at decade to century time scales. ?? 2011 Geological Society of America.

Response of C3 and C4 plants to middle-Holocene climatic variation near the prairie-forest ecotone of Minnesota, U.S.A.

Energy Technology Data Exchange (ETDEWEB)

Tian, J; Brown, T A; Hu, F S; Stefanova, I; Nelson, D M

2003-12-24

Paleorecords of the middle Holocene (MH) from the North American midcontinent can offer insights into ecological responses to pervasive drought that may accompany future climatic warming. We analyzed MH sediments from West Olaf Lake (WOL) and Steel Lake (SL) in Minnesota to examine the effects of warm/dry climatic conditions on prairie-woodland ecosystems. Mineral composition and carbonate {delta}{sup 18}O were used to determine climatic variations, whereas pollen assemblages, charcoal {delta}{sup 13}C, and charcoal accumulation rates were used to reconstruct vegetation composition, C{sub 3} and C{sub 4} plant abundance, and fire. The ratio of aragonite:calcite at WOL and {delta}{sup 18}O at SL suggest that pronounced droughts occurred during the MH but that drought severity decreased with time. From charcoal {delta}{sup 13}C data we estimated that the MH abundance of C{sub 4} plants averaged 50% at WOL and 43% at SL. At WOL C{sub 4} abundance was negatively correlated with aragonite:calcite, suggesting that severe moisture deficits suppressed C{sub 4} plants in favor of weedy C{sub 3} plants (e.g., Ambrosia). As climate ameliorated C{sub 4} abundance increased (from {approx}33 to 66%) at the expense of weedy species, enhancing fuel availability and fire occurrence. In contrast, farther east at SL climate was cooler and wetter than at WOL, and C{sub 4} abundance showed no correlation with {delta}{sup 18}O-inferred aridity. Woody C{sub 3} plants (e.g., Quercus) were more abundant, biomass flammability lower, and fires less important at SL than at WOL. Our results suggest that C{sub 4} plants are adapted to warm/dry climatic conditions, but not to extreme droughts, and that the fire regime is controlled by biomass-climate interactions.

An automated technique for measuring deltaD and delta18O values of porewater by direct CO2 and H2 equilibration.

Science.gov (United States)

Koehler, G; Wassenaar, L I; Hendry, M J

2000-11-15

The stable-oxygen and -hydrogen isotopic values (deltaD, delta18O) of porewater in geologic media are commonly determined on water obtained by extraction techniques such as centrifugation, mechanical squeezing, vacuum heating and cryogenic microdistillation, and azeotropic distillation. Each of these techniques may cause isotopic fractionation as part the extraction process and each is laborious. Here we demonstrate a new approach to obtain automated, high-precision deltaD and delta18O measurements of porewater in geologic sediments by direct H2- and CO2-porewater equilibration using a modified commercial CO2-water equilibrator. This technique provides an important and cost-effective improvement over current extraction methods, because many samples can be rapidly analyzed with minimal handling, thereby reducing errors and potential for isotopic fractionation. The precision and accuracy of direct H2- and CO2-porewater equilibration is comparable to or better than current porewater extraction methods. Finally, the direct equilibration technique allows investigators to obtain high-resolution (cm scale) porewater deltaD and delta18O profiles using cores from individual boreholes, eliminating the need for costly piezometers or conventional porewater extractions.

δ 18O of ethanol in wine and spirits for authentication purposes.

Science.gov (United States)

Perini, Matteo; Camin, Federica

2013-06-01

Since 1986 the European Union has established official isotopic analysis methods for detecting the illegal addition of sugar and water to wine and to enable geographical traceability. In this paper we investigate the possibility of using analysis of the 18O/16O stable isotope ratio (expressed as δ 18O) of ethanol to improve detection of the watering of wine and to determine the origin of ethanol. Sixty-nine authentic wine samples from all over Italy, 59 spirits from fruit and cereals, 5 chemically synthesized ethanols, one concentrated and rectified must, one beet and one cane sugar, one fresh must, and 6 waters with increasing δ 18O values were considered. Ethanol was recovered by distillation, using a Cadiot spinning band column, following the official OIV methods. The residual water was trapped by storing the distillate for at least 24 h on a molecular sieve. The 18O/16O ratio was measured using a pyrolyser interfaced with an isotope ratio mass spectrometer. The δ (-18)O of ethanol is significantly related to the δ 18O of the fermentation water and can be considered as a reliable internal reference. The values ranged from +24‰ to +36‰ in wine (years 2008 to 2012), +10‰ to +26‰ in fruit and cereal distillates, and from -2‰ to +12‰ in synthetic ethanol. The method was shown to be effective in improving detection of the watering of wine and determining the origin of ethanol (from grapes, other fruit, or synthesis), but not in detecting the addition of cane or beet sugar to wine. © 2013 Institute of Food Technologists®

Relation between D/H ratios and 18O /16O ratios in cellulose from linen and maize - Implications for paleoclimatology and for sindonology

Science.gov (United States)

DeNiro, Michael J.; Sternberg, Leonel D.; Marino, Bruno D.; Druzik, James R.

1988-09-01

The 18O /16O ratios of cellulose and the D/H ratios of cellulose nitrate were determined for linen, a textile produced from the fibers of the flax plant Linum usitatissimum, and for maize ( Zea mays) from a variety of geographic locations in Europe, the Middle East, and North and South America. The regression lines of δD values on δ 18O values had slopes of 5.4 and 5.8 for the two species. Statistical analysis of results reported in the only other study in which samples of a single species (the silver fir Abies pindrow) that grew under a variety of climatic conditions were analyzed yielded slopes of ~6 when δD values of cellulose nitrate were regressed on δ 18O values of cellulose. The occurrence of this previously unrecognized relationship in three species suggests it may obtain in other plants as well. Determining the basis for this relationship, which is not possible given current understanding of fractionation of the isotopes of oxygen and hydrogen by plants, should lead to increased understanding of how D/H and 18O /16O ratios in cellulose isolated from fossil plants are related to paleoclimates. The separation of most linen samples from Europe from those originating in the Middle East when δD values are plotted against δ 18O values suggests it may be possible to use the isotope ratios of cellulose prepared from the Shroud of Turin to resolve the controversy concerning its geographic origin.

Laser Spectroscopy Monitoring of 13C18O16O and 12C17O16O of Atmospheric Carbon Dioxide

Science.gov (United States)

Shorter, J. H.; Nelson, D. D.; Ono, S.; McManus, J. B.; Zahniser, M. S.

2017-12-01

One of the main challenges to making accurate predictions of future changes in CO2 concentration is the capability to determine what fraction of human produced CO2 remains in the atmosphere. We present our progress in the application of Tunable Infrared Laser Direct Absorption Spectroscopy (TILDAS) to the measurement of the primary clumped (13C18O16O) as well as 17O (12C17O16O) isotopologues of atmospheric CO2, as a tracer of its sources and sinks. We expect unique isotopologue signals in CO2 from high-temperature combustion sources, plants, soils, and air-sea exchange processes. High sampling frequency (a few minutes for each sample vs. reference cycle) achieved by a TILDAS instrument is expected to enable us to document local heterogeneous sources and temporal variations. The TILDAS is equipped with a newly developed 400-meter absorption cell. We designed a dual pressure measurement technique in which the clumped isotopologue, 13C18O16O, and 13C16O16O are first measured at 30 torr cell pressure. This is followed by measurement of 12C17O16O, 12C18O16O and 12C16O16O at lower ( 5 torr) cell pressure. Isotopologue ratios are compared between reference and sample gases. Preliminary tests demonstrated a precision approaching 0.03 ‰ for the ratio 13C18O16O/13C16O16O and 0.08‰ for Δ13C18O16O value (1σ repeatability for 4 min sample vs. reference cycle). Sample size for a single analysis is approximately 100 mL of air (1.6μmol of CO2). Given the previously observed range of variations for Δ13C18O16O and Δ17O values as large as 0.6 to 0.3 ‰, respectively, TILDAS offers a novel approach for real time monitoring of atmospheric CO2 isotopologues. It was found that achieving better than 0.1‰ requires careful matching of CO2 mixing ratios between reference and sample air. A primary cause of pressure and mixing ratio dependence is inaccurate baseline fitting (analogous to abundance sensitivity or pressure baseline for IRMS). Given that mixing ratios of atmospheric

Nuclear reactions induced by the bombardment of 18O with 18O

International Nuclear Information System (INIS)

Kalinsky, D.; Melnik, D.; Smilansky, U.; Trautner, N.; Horowitz, Y.; Mordechai, S.

1977-01-01

Angular distributions have been measured for the elastic, inelastic, one and two-neutron transfer reactions for the system 18 O + 18 O at center of mass energies ranging from 10.0 to 18.0 MeV, at c.m. angles between 90deg and 125deg. The inelastic scattering data were analyzed assuming a collective excitation mechanism and with a coupled channels approach. In order to obtain a good fit it was necessary to include a hexadecapole deformation. The one and two neutron transfer reactions were analyzed in terms of a single step finite range plus recoil DWBA theory. (author)

Isotopic geochronology of granitic rocks from the Central Iberian Zone: comparison of methodologies

Directory of Open Access Journals (Sweden)

Antunes, I. M.H.R.

2010-06-01

Full Text Available Five granitic rocks, concentrically disposed from core to rim, were distinguished in the Castelo Branco pluton. U-Pb-Th electron microprobe monazite ages from granitic rocks are similar and ranging between 297-303 Ma. The granitic rocks from Castelo Branco pluton are 310 ± 1 Ma old, obtained by U-Pb (ID-TIMS in separated zircon and monazite crystals, indicating a similar emplacement age for all granitic rocks of the pluton. Initial ⁸⁷Sr/⁸⁶Sr isotopic ratios and epsilon-Nd₃₁₀ and delta->18O values suggest three distinct pulses of granitic magma and that they are derived from partial melting of heterogeneous metasedimentary materials. The other granitic rocks are related by magmatic differentiation and show small variations in (⁸⁷Sr/⁸⁶Sr₃₁₀, epsilon-Nd₃₁₀ and delta->18O. The granitic pluton of Castelo Branco shows a rare reverse zoning.

En el plutón de Castelo Branco, se distinguen cinco granitoides, dispuestos concéntricamente de núcleo a borde del plutón. Las edades U-Pb-Th obtenidas en cristales de monacita por microsonda electrónica en estos granitoides son similares entre sí y varían entre 297 y 303 Ma. Los resultados de datación por U-Pb (ID-TIMS en cristales de circón y de monacita de los tres granitos seleccionados, indican una edad de implantación de 310 ± 1 Ma y que son rocas emplazadas simultáneamente. Las relaciones isotópicas iniciales de ⁸⁷Sr/⁸⁶Sr y los valores de epsilon-Nd₃₁₀ y delta->18O de los tres pulsos magmáticos son característicos de granitos resultantes de anatexia cortical a partir de rocas metasedimentarias heterogéneas. En la secuencia de diferenciación magmática, las rocas graníticas presentan pequeñas variaciones en (⁸⁷Sr/⁸⁶Sr₃₁₀, epsilon-Nd₃₁₀ y delta->18O. El plutón de Castelo Branco presenta un

Development and application of the mollusc Arctica islandica as a paleoceanographic tool for the North Atlantic Ocean

Energy Technology Data Exchange (ETDEWEB)

Weidman, C.R.

1995-09-01

Until now there has been no tool comparable to corals for reconstructing long term high-resolution geochemical time-series for the colder, higher-latitude oceans. In this thesis, the long-lived (+100 years) boreal mollusc (Bivalvia) Arctica islandica is shown to be practical for this purpose in the northern North Atlantic Ocean. The evidence, compiled here, demonstrates that the carbonate shell of this species faithfully records the ambient dissolved inorganic carbon`s (DIC) radiocarbon ({Delta}{sup 14}C) concentration and accurately reflects the ambient temperature in its stable oxygen isotope ({delta}{sup 18}O) composition. However, the stable carbon isotope ({delta}{sup 13}C) composition of the A. islandica shell likely is not a good recorder of ambient DIC {delta}{sup 13}C, and likely responds to physiological controls. Four {Delta}{sup 14}C time histories are reconstructed from the annual bands of A. islandica shells for the higher-latitudes of the northern North Atlantic Ocean (from 41{degree}N to 70{degree}N).

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.

Measurement of δ18O, δ17O, and 17O-excess in Water by Off-Axis Integrated Cavity Output Spectroscopy and Isotope Ratio Mass Spectrometry

Science.gov (United States)

Berman, Elena S.F.; Levin, Naomi E.; Landais, Amaelle; Li, Shuning; Owano, Thomas

2013-01-01

Stable isotopes of water have long been used to improve understanding of the hydrological cycle, catchment hydrology, and polar climate. Recently, there has been increasing interest in measurement and use of the less-abundant 17O isotope in addition to 2H and 18O. Off-axis integrated cavity output spectroscopy (OA-ICOS) is demonstrated for accurate and precise measurements δ18O, δ17O, and 17O-excess in liquid water. OA-ICOS involves no sample conversion and has a small footprint, allowing measurements to be made by researchers collecting the samples. Repeated (514) high-throughput measurements of the international isotopic reference water standard GISP demonstrate the precision and accuracy of OA-ICOS: δ18OVSMOW-SLAP =−24.74 ± 0.07 ‰ (1σ) and δ17OVSMOW-SLAP = −13.12 ± 0.05 ‰ (1σ). For comparison, the IAEA value for δ18OVSMOW-SLAP is −24.76 ± 0.09 ‰ (1σ) and an average of previously reported values for δ17OVSMOW-SLAP is −13.12 ± 0.06 ‰ (1σ). Multiple (26) high-precision measurements of GISP provide a 17O-excessVSMOW-SLAP of 23 ± 10 per meg (1σ); an average of previously reported values for 17O-excessVSMOW-SLAP is 22 ± 11 per meg (1σ). For all these OA-ICOS measurements, precision can be further enhanced by additional averaging. OA-ICOS measurements were compared with two independent isotope ratio mass spectrometry (IRMS) laboratories and shown to have comparable accuracy and precision as the current fluorination-IRMS techniques in δ18O, δ17O, and 17O-excess. The ability to measure accurately δ18O, δ17O, and 17O-excess in liquid water inexpensively and without sample conversion is expected to increase vastly the application of δ17O and 17O-excess measurements for scientific understanding of the water cycle, atmospheric convection, and climate modeling among others. PMID:24032448

40 CFR 35.935-18 - Value engineering.

Science.gov (United States)

2010-07-01

... 40 Protection of Environment 1 2010-07-01 2010-07-01 false Value engineering. 35.935-18 Section 35.935-18 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY GRANTS AND OTHER FEDERAL ASSISTANCE... engineering. A grantee must comply with the applicable value engineering requirements of § 35.926. ...

Reef coral δ18O thermometer in Hainan island waters, south China sea

International Nuclear Information System (INIS)

He Xuexian; Peng Zicheng; Wang Zhaorong; Huo Weiguo; Tan Jun; Nie Baofu; Chen Tegu; Zhong Jinliang

2000-01-01

An 18-year-long (1981-1998) study was conducted in Hainan Island waters (22 degree 22'N, 110 degree 39'E) to determine the relationship between δ 18 O in skeletal aragonite carbonate and sea surface temperature (SST) in porites lutea of reef-building corals. δ 18 O values in skeletal aragonite carbonate were measured by means of mass spectrometry. Coral samples grew at 5 m depth at Longwan Bay. Monthly measurements of the SST from 1960 to 1998 were taken at Qinglan Bay adjacent to the place of the collected samples. The thermometer shows that SST = -4.16 δ 18 O PDB + 4.9 (r = 0.80) and dδ 18 O/dT = -0.24 per mil/degree C. The δ 18 O thermometer is strongly influenced by the rainfall and runoff. Using the thermometer, the SST in the past hundred years with monthly resolution will be reconstructed and the climatic change in the northern area of South China Sea will be hind cast

Mahe, Seychelles Stable Isotope (delta 18O) Data for 1846 to 1995

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Seychelles coral oxygen-18 time series, data are monthly values of d18O from July 1846 to February 1995 from a 3-m Porites lutea coral colony collected from Beau...

Ostracod calcite records the 18O/16O ratio of the bicarbonate and carbonate ions in water

Science.gov (United States)

Devriendt, Laurent S.; McGregor, Helen V.; Chivas, Allan R.

2017-10-01

The δ18O of ostracod valves is widely used to infer water δ18O and temperature. However, ostracod δ18O appears sensitive to other environmental variables. In addition, there is species-dependent ostracod calcite 18O enrichment, relative to slowly precipitated inorganic calcite under the same conditions. Together these uncertainties complicate ostracod paleoclimate reconstructions. This study presents a new understanding of the causes of ostracod δ18O variations based on a global database of published ostracod δ18O values in lake, marine and coastal environments, and from culture experiments. The database includes associated field/experiment host water parameters including temperature (-1 to 32 °C), water δ18O (-13.2‰ to 4.3‰ VSMOW), pH (6.9-10.4), salinity (0-72 g/kg), calcite saturation states (0.6-26), and dissolved inorganic carbon concentration [DIC] (0.9-54.3 mmol/kg). The data show that: (1) the δ18O of marine and non-marine ostracods reflects the 18O/16O of the sum of host water CO32- and HCO3- ions. For example, at a given temperature, the δ18O of non-marine ostracods decreases by 4‰ to 6‰ as [CO32-]/[DIC] reaches 70%, depending on the ostracod species. In low [CO32-]/[DIC] settings (i.e. high HCO3-/CO32-), ostracod 18O/16O is close to the 18O/16O of HCO3- ions, which explains why on average ostracod δ18O is higher than the δ18O of inorganic calcite precipitated slowly under the same conditions. (2) Taxonomic offsets in ostracod δ18O vary with the host water [CO32-]/[DIC]. In environments where HCO3- ≫ CO32- (i.e. most freshwater lakes), the 18O/16O of Candonids is indistinguishable from the 18O/16O of HCO3- ions (difference of 0.10 ± 0.16‰) while the 18O/16O of Cyprids is lower than the 18O/16O of HCO3- ions by -0.77‰ to -0.32‰, Cytherids by -0.88 ± 0.29‰, and Limnocytherids by -1.12 ± 0.05‰. (3) The sensitivity of ostracod δ18O to [CO32-]/[DIC] also varies with taxonomy. For each percent increase in [CO32-]/[DIC

Growth and {delta}{sup 13}C responses to increasing atmospheric carbon dioxide concentrations for several crop species

Energy Technology Data Exchange (ETDEWEB)

Hanba, Y.T.; Wada, E. [Center for Ecological Research, Kyoto University, Kyoto (Japan); Osaki, M.; Nakamura, T. [Faculty of Agriculture, Hokkaido University, Hokkaido (Japan)

1996-04-01

The responses of plant growth and carbon isotope discrimination ({Delta}) to elevated atmospheric CO{sub 2} concentrations for several crop species (lettuce: Lactuca sativa L.; corn: Zea Mays L. var. P3540, wheat: Triticum aestivum L. var Haruyutaka; and soybean: Glycine Max (L). Merr. var. Kitamusume) were investigated. Shoot relative growth rate was used to indicate plant growth, and {delta}{sup 13}C value of leaf materials in corn (C4 species) was used to calculate {Delta} for C3 species. Plant growth was stimulated by enriched CO{sub 2}, while {Delta} remained almost constant as CO{sub 2} concentration changed. {Delta} showed interspecific difference, and the plant species of larger {Delta} had larger relative growth rates. Relative growth rates of the plants of larger {Delta} were stimulated by CO{sub 2} enrichment more than those of the plants of smaller {Delta}. We propose that plant {Delta} could be a possible parameter to assess the interspecific difference of plant response to the increasing atmospheric CO{sub 2} concentrations. 3 figs., 2 tabs., 25 refs.

Simultaneous analysis of 17O/16O, 18O/16O and 2H/1H of gypsum hydration water by cavity ring‐down laser spectroscopy

Science.gov (United States)

Mather, Ian; Rolfe, James; Evans, Nicholas P.; Herwartz, Daniel; Staubwasser, Michael; Hodell, David A.

2015-01-01

Rationale The recent development of cavity ring‐down laser spectroscopy (CRDS) instruments capable of measuring 17O‐excess in water has created new opportunities for studying the hydrologic cycle. Here we apply this new method to studying the triple oxygen (17O/16O, 18O/16O) and hydrogen (2H/1H) isotope ratios of gypsum hydration water (GHW), which can provide information about the conditions under which the mineral formed and subsequent post‐depositional interaction with other fluids. Methods We developed a semi‐automated procedure for extracting GHW by slowly heating the sample to 400°C in vacuo and cryogenically trapping the evolved water. The isotopic composition (δ17O, δ18O and δ2H values) of the GHW is subsequently measured by CRDS. The extraction apparatus allows the dehydration of five samples and one standard simultaneously, thereby increasing the long‐term precision and sample throughput compared with previous methods. The apparatus is also useful for distilling brines prior to isotopic analysis. A direct comparison is made between results of 17O‐excess in GHW obtained by CRDS and fluorination followed by isotope ratio mass spectrometry (IRMS) of O2. Results The long‐term analytical precision of our method of extraction and isotopic analysis of GHW by CRDS is ±0.07‰ for δ17O values, ±0.13‰ for δ18O values and ±0.49‰ for δ2H values (all ±1SD), and ±1.1‰ and ±8 per meg for the deuterium‐excess and 17O‐excess, respectively. Accurate measurement of the 17O‐excess values of GHW, of both synthetic and natural samples, requires the use of a micro‐combustion module (MCM). This accessory removes contaminants (VOCs, H2S, etc.) from the water vapour stream that interfere with the wavelengths used for spectroscopic measurement of water isotopologues. CRDS/MCM and IRMS methods yield similar isotopic results for the analysis of both synthetic and natural gypsum samples within analytical error of the two methods. Conclusions We

Low-energy reaction yields for 18O(p,γ) and 18O(α,γ)

International Nuclear Information System (INIS)

Vogelaar, R.B.; Wang, T.R.; Kellogg, S.E.; Kavanagh, R.W.

1990-01-01

Resonance yields, γ-ray branching, and low-energy limits have been measured for 18 O(p,γ) and 18 O(α,γ), for E p α <0.78 MeV, using a 4π array of NaI detectors. The results confirm previous resonance strengths, and set additional constraints on possible low-energy contributions to stellar reaction rates

Pulmonary NO and C18O2 uptake during pressure-induced lung expansion in rabbits.

Science.gov (United States)

Heller, Hartmut; Schuster, Klaus-Dieter

2007-01-01

In artificially ventilated animals we investigated the dependence of the pulmonary diffusing capacities of nitric oxide (NO) and doubly 18O-labeled carbon dioxide (DLNO, DLC18O2) on lung expansion with respect to ventilator-driven increases in intrapulmonary pressure. For this purpose we applied computerized single-breath experiments to 11 anesthetized paralyzed rabbits (weight 2.8-3.8 kg) at various alveolar volumes (45-72 ml) by studying the almost entire inspiratory limb of the respective pressure/volume curves (intrapulmonary pressure: 6-27 cmH2O). The animals were ventilated with room air, employing a computerized ventilatory servo-system that we designed to maintain mechanical ventilation and to execute the particular lung function tests automatically. Each single-breath maneuver was started from residual volume (13.5+/-2 ml, mean+/-SD) by inflating the rabbit lungs with 35-55 ml indicator gas mixture containing 0.05% NO in N2 or 0.9% C18O2 in N2. Alveolar partial pressures of NO and C18O2 were measured by respiratory mass spectrometry. Values of DLNO and DLC18O2 ranged between 1.55 and 2.49 ml/(mmHg min) and 11.7 and 16.6 ml/(mmHg min), respectively. Linear regression analyses yielded a significant increase in DLNO with simultaneous increase in alveolar volume (Pvolume on DLC18O2 values.

18 CFR 801.11 - Public values.

Science.gov (United States)

2010-04-01

... 18 Conservation of Power and Water Resources 2 2010-04-01 2010-04-01 false Public values. 801.11... POLICIES § 801.11 Public values. (a) The basin has many points of archeological and historic interest, and... value of these areas cannot be measured simply in economic terms and will strive to preserve and promote...

High-precision determination of 18O/16O ratios of silver phosphate by EA-pyrolysis-IRMS continuous flow technique.

Science.gov (United States)

Lécuyer, Christophe; Fourel, François; Martineau, François; Amiot, Romain; Bernard, Aurélien; Daux, Valérie; Escarguel, Gilles; Morrison, John

2007-01-01

A high-precision, and rapid on-line method for oxygen isotope analysis of silver phosphate is presented. The technique uses high-temperature elemental analyzer (EA)-pyrolysis interfaced in continuous flow (CF) mode to an isotopic ratio mass spectrometer (IRMS). Calibration curves were generated by synthesizing silver phosphate with a 13 per thousand spread in delta(18)O values. Calibration materials were obtained by reacting dissolved potassium dihydrogen phosphate (KH(2)PO(4)) with water samples of various oxygen isotope compositions at 373 K. Validity of the method was tested by comparing the on-line results with those obtained by classical off-line sample preparation and dual inlet isotope measurement. In addition, silver phosphate precipitates were prepared from a collection of biogenic apatites with known delta(18)O values ranging from 12.8 to 29.9 per thousand (V-SMOW). Reproducibility of +/- 0.2 per thousand was obtained by the EA-Py-CF-IRMS method for sample sizes in the range 400-500 microg. Both natural and synthetic samples are remarkably well correlated with conventional (18)O/(16)O determinations. Silver phosphate is a very stable material and easy to degas and, thus, could be considered as a good candidate to become a reference material for the determination of (18)O/(16)O ratios of phosphate by high-temperature pyrolysis. Copyright 2006 John Wiley & Sons, Ltd.

Decreasing Asian summer monsoon intensity after 1860 AD in the global warming epoch

Energy Technology Data Exchange (ETDEWEB)

Xu, Hai [Institute of Earth Environment, Chinese Academy of Sciences, State Key Laboratory of Loess and Quaternary Geology, Xi' an, Shaanxi Province (China); Hong, Yetang; Hong, Bin [Institute of Geochemistry, Chinese Academy of Sciences, State Key Laboratory of Environmental Geochemistry, Guiyang (China)

2012-10-15

The trend of the Indian summer monsoon (ISM) intensity and its nature during the past 100 and 200 years still remain unclear. In this study we reconstructed the ISM intensity during the past 270 years from tree ring {delta}{sup 18}O at Hongyuan, eastern edge of the Tibet Plateau. The monsoon failures inferred from {delta}{sup 18}O{sub tree} {sub ring} correlate well with those recorded in ice cores, speleothem, and historical literature sources. 22.6, 59.0, and 110.9-years frequency components in the Hongyuan {delta}{sup 18}O{sub tree} {sub ring} series, which may be the responses to solar activities, synchronize well with those recorded in other ISM indices. A notable feature of the reconstructed ISM intensity is the gradually decreasing trend from about 1860 to the present, which is inversely related to the increasing temperature trend contemporaneously. Such ''decreasing ISM intensity-increasing temperature'' tendency can also be supported by ice core records and meteorological records over a wide geographic extension. The decrease in sea surface temperature gradient between tropical and north Indian Ocean, and the decrease in land-sea thermal contrast between tropical Indian Ocean and ''Indian sub-continent-western Himalaya'' are possibly responsible for the observed decreasing ISM trend. (orig.)

Oil generation potential assessment and paleoenvironmental interpretation based on bio markers and stable carbon isotopes of the Pliensbachian - lower Toarcian (Lower Jurassic) of the Peniche region (Lusitanian Basin, Portugal); Avaliacao do potencial gerador de petroleo e interpretacao paleoambiental com base em biomarcadores e isotopos estaveis de carbono da secao Pliensbaquiano - Toarciano inferior (Jurassico Inferior) da regiao de Peniche (Bacia Lusitanica, Portugal)

Energy Technology Data Exchange (ETDEWEB)

Oliveira, Luiz Carlos Veiga de; Rodrigues, Rene; Duarte, Luis Vitor; Lemos, Valesca Brasil [PETROBRAS, Rio de Janeiro, RJ (Brazil). Centro de Pesquisas (CENPES). Gerencia de Bioestratigrafia e Paleoecologia]. E-mail: lcveiga@petrobras.com.br

2006-05-15

The Lusitanian Basin (Portugal) is located on the western margin of the Iberian Plate with maximum sedimentary thickness around 5 km. In spite of containing promising petroleum systems and more than a hundred wells, its hydrocarbon generation potential has not been fully evaluated yet. These sediments range from upper Triassic to upper Cretaceous, mainly from the Jurassic age. The Lower Jurassic is particularly well represented in the Lusitanian Basin, specifically in the Peniche region, where there are more than 450 m thick outcrops of carbonate rocks aged between Sinemurian and Toarcian. This study presents the evaluation of the hydrocarbon generation potential of the Pliensbachian . lower Toarcian of the Peniche section; which includes the Vale das Fontes Formation, Lemede Formation and Cabo Carvoeiro Formation (CC1 and CC2 members) based on 233 rock samples analyzed for total organic carbon (TOC), Rock-Eval pyrolysis and bio markers. Available data of oxygen and carbon stable isotopes were also used in the paleoenvironmental interpretation. Marls and limestones with the bituminous facies (Mlbf) of the Vale das Fontes Formation, present the highest TOC values, up to 14.95%, corresponding to the ibex (upper part), davoei and margaritatus ammonites zones and part of the NJ4a and NJ4b nanno fossils bio zones (Pliensbachian). In thermal immature sections (T max about 430 deg C), this member also shows high S{sub 2} values (10 to 50 mgHC/g rock) and Hydrogen index (HI: 200 to 555 mgHC/g TOC). The correlation between HI x OI shows that type II kerogen is predominant in the portion of the section where TOC values are higher. The good positive correlation between TOC values and the bio markers ratio P/nC17 and sterane (C{sub 27}/C{sub 29}) throughout the Mlbf Member suggests a gradual increase of anoxia and higher contribution of algae in relation to terrestrial organic matter. Usually {delta}{sup 18}O variations observed in the basins of the Iberian Peninsula have been

Seasonal Climate Profiles of an Ice-free Arctic Based on Intra-ring Analyses of δ18O Value in Fossil Wood

Science.gov (United States)

Schubert, B.; Jahren, A. H.

2017-12-01

Arctic sea ice thickness and extent are projected to continue their substantial decline during this century, with an 80% reduction in sea-ice extent by 2050. While there is a clear relationship between mean annual temperature (MAT) and the concentration of atmospheric carbon dioxide (pCO2) across both glacial and interglacial periods, data on seasonal fluctuations is limited. Here we report seasonal temperature estimates for the Arctic during the ice-free conditions of the late early to middle Eocene based upon exquisitely preserved, mummified wood collected from Banks Island, Northwest Territories, Canada ( 74 oN). Annual growth rings identified in the wood specimens were subdivided by hand at sub-millimeter resolution and cellulose was extracted from each sub-sample for determination of stable oxygen isotope (δ18O) value (n = 81). The data reveal a consistent, cyclic pattern of decreasing and increasing δ18O value up to 3‰ across growth rings that was consistent with patterns observed in other modern and fossil wood, including from other high latitude sites. From these data we quantified cold month and warm month seasonal temperatures using a previously published model (Schubert and Jahren, 2015, QSR, 125: 1-14). Our calculations revealed low overall seasonality in the Arctic during the Eocene with above-freezing winters and mild summers, consistent with the presence of high biomass temperate rainforests. These results highlight the importance of warm winters in maintaining ice-free conditions in the Arctic and suggest that increased winter temperatures in today's Arctic in response to rising pCO2 will be of particular importance for Arctic ice-loss.

Geological setting, isotope studies (C, O and Pb) and associated metals in the Tocantinzinho gold deposit, Tapajos domain, Tapajos-Parima Province; Contexto geologico, estudos isotopicos (C, O e Pb) e associacao metalica do deposito aurifero Tocantinzinho, dominio Tapajos, Provincia Tapajos-Parima

Energy Technology Data Exchange (ETDEWEB)

Villas, Raimundo Netuno Nobre [Universidade Federal do Para (UFPA), Belem, PA (Brazil); Santiago, Erika Suellen Barbosa; Castilho, Marilia Portela, E-mail: netuno@ufpa.br, E-mail: esbsantiago@gmail.com, E-mail: castilho.marilia@hotmail.com [Universidade Federal do Para (UFPA), Belem, PA (Brazil). Inst. de Geociencias. Programa de Pos-graduacao em Geologia e Geoquimica

2013-03-15

The Tocantinzinho ore deposit is located along a NW-SE-trending lineament, southwestern of Itaituba (Para, Brazil), and is the largest known gold deposit of the Tapajos Province. The host Tocantinzinho granite is essentially isotropic and dominated by syenogranites and monzogranites that have been weakly to moderately altered by hydrothermal fluids. Microclinization (earliest), chloritization, sericitization, silicification and carbonatization (latest) are the main types of alteration. Most mineralization was contemporaneous with the sericitization/silicification and is represented by sulfide- and gold-bearing veinlets which locally occur as stockwork. Pyrite, chalcopyrite, sphalerite and galena are the most common sulfides. Among the ore metals, Cu, Pb and Zn present the highest contents, but Mo, As and Bi locally show anomalous concentrations. The relationship of Au with Cu, Pb or Zn is at random and the Au/Ag ratios range from 0.05 to 0.5. The higher the sulfide contents, the higher the Au concentrations, though it occurs mainly included in pyrite. Zircon monocrystals from the Tocantinzinho granite yielded an average Pb-Pb age of 1982 {+-}8Ma and may represent an earlier event of the Creporizao magmatic arc. {delta}{sup 13}C{sub PDB} values for calcite from the carbonatization stage fall dominantly between -3.45 and -2.29 Per-Mille-Sign , being compatible with a deep crustal source that may include carbonatite reservoirs. In turn, {delta}{sup 18}O{sub SMOW} values vary from +5.97 to +14.10 Per-Mille-Sign , being indicative of magmatic derivation, although the less positive values suggest contribution from surficial waters. Unpublished fluid inclusion study reveals the presence of aquo-carbonic fluids, whose CO{sub 2} could have been dissolved in the granitic magma rather than being related to the shear zone. The available data allow the Tocantinzinho deposit to be classified as a granite-hosted, intrusion-related gold deposit. (author)

Isotopic study of water exchange between atmosphere and biosphere at different sites in Pakistan

International Nuclear Information System (INIS)

Fazil, M.; Ali, M.; Ahmad, M.; Latif, Z.; Butt, S.; Choudhry, M.A.; Qureshiu, R.M.

2009-11-01

Study of Isotopic behavior of water exchange between atmosphere and biosphere was initiated to understand the ties between these two spheres. This report presents the isotopic data of delta/sup 18/O and delta /sup 2/H in the water contents of leaves and stems in different plant species along with soil moisture. Non woody plants of wheat and grass along with soil from the surface and from the depth of 7 cm were collected during January 2005 to April 2005. Woody plants of many species were sampled from two sites near Islamabad and Lahore. Air moisture was also collected in the field. Moisture contents from these samples were extracted using the vacuum distillation method and analyzed for /sup 18/O and /sup 2/H Data depicts that the /sup 18/O and /sup 2/H of moisture in the leaves of non- woody and woody plants are much more enriched than their respective stems. This behavior is due to the evaporative enrichment trend originating from the soil moisture in the active root zone and also from the surface of the leaf. Degree of enrichment depends on the size of leaves, temperature, wind speed, stomatal resistance, soil chemistry and humidity. Significant evaporation effects in the moisture of grass stems are due to photosynthesis. Reflection of typical isotopic values of individual rain events is also observed in soil, plant water and atmospheric moisture, which can be used for studying water-use efficiency. Leaves of woody plants have relatively depleted/sup 18/O values during wet (monsoon) period mainly due to retardation of fractionation resulting from higher humidity. The stem samples do not show any significant variation in delta/sup 18/O indicating no evaporation from stems of big trees. Degree of enrichment of leave samples of woody plants also indicates the species- specific effects in oxygen and hydrogen isotopes during transpiration. Pine and Eucalyptus leaves show more variation in the isotopic contents as compared to other species. (author)

Regional cerebral blood flow measurement with intravenous [15O]water bolus and [18F]fluoromethane inhalation

International Nuclear Information System (INIS)

Herholz, K.; Pietrzyk, U.; Wienhard, K.; Hebold, I.; Pawlik, G.; Wagner, R.; Holthoff, V.; Klinkhammer, P.; Heiss, W.D.

1989-01-01

In 20 patients with ischemic cerebrovascular disease, classic migraine, or angiomas, we compared paired dynamic positron emission tomographic measurements of regional cerebral blood flow using both [ 15 O]water and [ 18 F]fluoromethane as tracers. Cerebral blood flow was also determined according to the autoradiographic technique with a bolus injection of [ 15 O]water. There were reasonable overall correlations between dynamic [ 15 O]water and [ 18 F]fluoromethane values for cerebral blood flow (r = 0.82) and between dynamic and autoradiographic [ 15 O]water values for cerebral blood flow (r = 0.83). We found a close correspondence between abnormal pathologic findings and visually evaluated cerebral blood flow tomograms obtained with the two tracers. On average, dynamic [ 15 O]water cerebral blood flow was 6% lower than that measured with [ 18 F]fluoromethane. There also was a general trend toward a greater underestimation with [ 15 O]water in high-flow areas, particularly in hyperemic areas, probably due to incomplete first-pass extraction of [ 15 O]water. Underestimation was not detected in low-flow areas or in the cerebellum. Absolute cerebral blood flow values were less closely correlated between tracers and techniques than cerebral blood flow patterns. The variability of the relation between absolute flow values was probably caused by confounding effects of the variation in the circulatory delay time. The autoradiographic technique was most sensitive to this type error

High-18O granitic plutons from the Frontenac Axis, Grenville Province of Ontario, Canada

International Nuclear Information System (INIS)

Shieh, Y.-N.

1985-01-01

18 O/ 16 O ratios have been determined for whole rock as well as coexisting minerals from nine syn- to post-tectonic monzonite and quartz monzonite plutons in the Westport-Gananoque area covering approximately 2500 km 2 . The plutons fall into two distinct isotopic groups: (I) Low- 18 O group: Rideau Lake, Westport, and Wolfe Lake plutons and (II) High- 18 O group: Lyndhurst, Perth Road, Battersea, Gananoque, South Lake and Crow Lake plutons. The 18 O/ 16 O ratios of granitic rocks from the latter group are among the highest ever reported in the literature. The isotopic compositions of samples within each pluton bear no relationship to the sample distance from the intrusive contacts nor are they affected by the types of country rocks into which they are emplaced. Oxygen isotope fractionations among coexisting quartz, feldspar, biotite and magnetite all show normal plutonic values. Thus, all lines of evidence suggest that the monzonite and quartz monzonite plutons did not acquire their characteristic 18 O/ 16 O ratios at the present level of exposure, either by isotopic exchange with the surrounding metasedimentary country rocks or by any post-crystallization low-temperature alteration processes. The results are discussed. (author)

Two-neutron stripping in ({sup 18}O, {sup 16}O) and (t,p) reactions

Energy Technology Data Exchange (ETDEWEB)

Cavallaro, M.; Agodi, A.; Carbone, D.; Cunsolo, A. [INFN - Laboratori Nazionali del Sud, Via S. Sofia 62, I-95125 Catania (Italy); Bondì, M.; Cappuzzello, F.; Nicolosi, D.; Tropea, S. [INFN - Laboratori Nazionali del Sud, Via S. Sofia 62, I-95125 Catania, Italy and Dipartimento di Fisica e Astronomia, Università di Catania, Via S. Sofia 64, I-95125 Catania (Italy); Borello-Lewin, T.; Rodrigues, M. R. D. [Instituto de Física - Universidade de São Paulo, Rua do Matão Travessa R Nr.187 CEP 05508-090 Cidade Universitária, São Paulo (Brazil); De Napoli, M. [INFN - Sezione di Catania, Via S. Sofia 64, I-95125 Catania (Italy); Garcia, V. N. [Instituto de Física, Universidade Federal Fluminense, Avenida Litoranea s/n, Gragoata, 24210-340, Niteroi, RJ (Brazil); Linares, R.; Lubian, J.; Paes, B. [Instituto de Física, Universidade Federal Fluminense, Avenida Litoranea s/n, Gragoata , 24210-340, Niteroi, RJ (Brazil); Foti, A. [Dipartimento di Fisica e Astronomia, Università di Catania, Via S. Sofia 64, I-95125 Catania, Italy and INFN - Sezione di Catania, Via S. Sofia 64, I-95125 Catania (Italy)

2014-11-11

The {sup 12}C({sup 18}O,{sup 16}O){sup 14}C reactions has been investigated at 84 MeV incident energy. The charged ejectiles produced in the reaction have been momentum analyzed and identified by the MAGNEX magnetic spectrometer. Q-value spectra have been extracted with an energy resolution of 160 keV (Full Width at Half Maximum) and several known bound and resonant states of {sup 14}C have been identified up to 15 MeV. In particular, excited states with dominant 2p - 4h configuration are the most populated. The absolute values of the cross sections have been extracted showing a striking similarity with those measured for the same transitions by (t,p) reactions. This indicates that the effect of the {sup 16}O core is negligible in the reaction mechanism.

Structure of 19O from measurement and R-matrix analysis of sigma(theta) for 18O(n,n)18O and 18O(n,n')18Osup(*) (1.98 MeV)

International Nuclear Information System (INIS)

Koehler, P.E.; Knox, H.D.; Resler, D.A.; Lane, R.O.

1986-01-01

Differential cross sections for neutrons elastically scattered from 18 O and inelastically scattered to the first excited state 18 Osup(*) (1.98 MeV) have been measured at forty-two incident energies for 5.0 19 O of 8.7 to 11.1 MeV. The cross sections were measured at eleven laboratory angles per energy from 20 0 to 160 0 and show considerable resonance structure. These new elastic and inelastic 1.98 MeV level data have been analyzed together with previously published cross sections for 0 19 O. The new assignments are compared to previous work where possible. Several previous assignments for resonances in the 0 19 F for the newly assigned levels in 19 O. On the basis of spin, parity, excitation energy and a comparison of reduced neutron widths in 19 O with reduced proton widths in 19 F, six previously-identified T=3/2 analogs were verified and eight new T=3/2 analogs were tentatively assigned. Comparisons with existing theoretical work are discussed. (orig.)

Automated calibration of laser spectrometer measurements of δ18 O and δ2 H values in water vapour using a Dew Point Generator.

Science.gov (United States)

Munksgaard, Niels C; Cheesman, Alexander W; Gray-Spence, Andrew; Cernusak, Lucas A; Bird, Michael I

2018-06-30

Continuous measurement of stable O and H isotope compositions in water vapour requires automated calibration for remote field deployments. We developed a new low-cost device for calibration of both water vapour mole fraction and isotope composition. We coupled a commercially available dew point generator (DPG) to a laser spectrometer and developed hardware for water and air handling along with software for automated operation and data processing. We characterised isotopic fractionation in the DPG, conducted a field test and assessed the influence of critical parameters on the performance of the device. An analysis time of 1 hour was sufficient to achieve memory-free analysis of two water vapour standards and the δ 18 O and δ 2 H values were found to be independent of water vapour concentration over a range of ≈20,000-33,000 ppm. The reproducibility of the standard vapours over a 10-day period was better than 0.14 ‰ and 0.75 ‰ for δ 18 O and δ 2 H values, respectively (1 σ, n = 11) prior to drift correction and calibration. The analytical accuracy was confirmed by the analysis of a third independent vapour standard. The DPG distillation process requires that isotope calibration takes account of DPG temperature, analysis time, injected water volume and air flow rate. The automated calibration system provides high accuracy and precision and is a robust, cost-effective option for long-term field measurements of water vapour isotopes. The necessary modifications to the DPG are minor and easily reversible. Copyright © 2018 John Wiley & Sons, Ltd.

O(18) revived

International Nuclear Information System (INIS)

Bagger, J.; Dimopoulos, S.; Masso, E.

1984-08-01

We present an O(18) theory which is pertubatively unifiable and which accounts for the absence of right-handed families in the low-energy world. The model gives rise to dramatic predictions for proton decay and for the Z 0 width

The enigma of effective pathlength for 18O enrichment in leaf water of conifers

Science.gov (United States)

Roden, J. S.; Kahmen, A.; Buchmann, N. C.; Siegwolf, R. T.

2013-12-01

-Gordon) overestimated leaf water δ18O. A single species-specific value for L could not be determined as the fractional difference between modeled and measured leaf water δ18O did not increase with E as theory predicts. Accounting for potentially unenriched water in vascular and transfusion tissues as well as a Péclet correction that allows the value for L to change with E (as in Song et al., 2013) produced accurate predictions of leaf water δ18O. Estimates of L (for a given E) were positively correlated with mean mesophyll thickness, which to our knowledge is the first time L has been related to a leaf anatomical measure. We repeated the experiment using young needles with much higher values for E, and found a continuing trend of reduced fractional difference with E, implying that Péclet corrections may need to be modified to predict conifer needle water over the range of needle phenology and physiology. Our study will help to better quantify effective pathlength and needle water δ18O in conifers, which are some of the most important organisms used for paleoclimate reconstruction.

Identification of nitrate sources in Taihu Lake and its major inflow rivers in China, using δ(15)N-NO(3)(-) and δ(18)O-NO(3)(-) values.

Science.gov (United States)

Chen, Zi-Xiang; Liu, Guang; Liu, Wei-Guo; Lam, Michael H W; Liu, Gui-Jian; Yin, Xue-Bin

2012-01-01

In the present study, δ(15)N and δ(18)O-NO(3)(-) values, as well as concentrations of some major ion tracers were determined in seasonal water samples from Taihu Lake and major watersheds to investigate the temporal and spatial variations of nitrate sources and assess the underlying nitrogen (N) biogeochemistry process. The results lead to the conclusion that the nitrate concentrations in Taihu Lake are lower in summer than that in winter due to the dilution effect of wet deposition. In winter, sewage and manure were the primary nitrate sources in major inflow rivers and North Taihu Lake (NTL), while nitrate sources in East Taihu Lake (ETL) probably derived from soil organic N. In summer, atmospheric deposition and sewage/manure inputs appear to play an important role in controlling the distribution of nitrates in the whole lake. The δ(18)O-NO(3)(-) values suggest that the nitrate produced from microbial nitrification is another major nitrate source during both winter and summer months. The variations in isotopic values in nitrate suggest denitrification enriched the heavier isotopes of nitrate in NTL in winter and in ETL in summer.

Coupled channel effects in quasi-elastic barrier distributions of 16,18O + 206Pb systems

International Nuclear Information System (INIS)

Jha, V.; Roy, B.J.; Parkar, V.V.; Kumawat, H.; Pal, U.K.; Pandit, S.K.; Mahata, K.; Shrivastava, A.; Mohanty, A.K.

2013-01-01

The fusion barrier distribution and QEBD for the 16 O + 208 Pb have been studied in great detail. The couplings due to the collective excitations of the colliding nuclei are found to have the dominant effect as deduced by the conventional coupled-channels calculations used to explain the experimental QEBD and fusion barrier distributions. In contrast, for the 18 O + 206 Pb system, the role of single neutron stripping (Q-value= -1.308 MeV) and neutron pair transfer (Q-value = + 1.917 MeV) are expected to be significant. In the present work, the QEBD measurements for the 18 O + 206 Pb system are performed for the investigation of these aspects

A urinary metabolite of {Delta}{sup 1}-tetrahydrocannabinol. The first synthesis of 4``-hydroxy-{Delta}{sup 1}-tetrahydrocannabinol-7-oic acid labelled with deuterium

Energy Technology Data Exchange (ETDEWEB)

Szirmai, Maria; Odqvist, Helena [Uppsala Univ. (Sweden). Dept. of Pharmacognosy; Halldin, M.M. [Karolinska Inst., Stockholm (Sweden). Dept. of Pharmacology

1996-04-01

The first synthesis of 4``-hydroxy-{Delta}-{sup 1}-THC-7-oic acid, one of the three major metabolites of {Delta}{sup 1}-THC identified in human urine is discussed. Methyl 4-(3,5-dihydroxyphenyl)butanoate was prepared from 3,5-diydroxybenzoic acid in an overall yield of 15% was condensed with a terpene synthon under acidic conditions followed by hydrolysis and conversion of the 4``-carboxylic acid function to the corresponding methyl ketone using methyllithium. Reduction with NaBH{sub 4} afforded the secondary alcohol in the side-chain. Acetylation and removal of the 1,3-dithiane masking group gave the aldehyde in C-7-position which was further oxidized using NaClO{sub 2} followed by deacetylation to give the desired metabolite. The same procedure may be used for the synthesis of unlabelled 4``-hydroxy-{Delta}{sup 1}-THC-7-oic acid. (author).

Laser-based measurements of 18O/16O stable isotope ratios (δ18O in wine samples

Directory of Open Access Journals (Sweden)

Gupta M

2013-09-01

Full Text Available Manish Gupta,1 J Brian Leen,1 Elena Simone Franklin Berman,1 Aldo Ciambotti2 1Los Gatos Research, Mountain View, CA, USA; 2Consiglio per la Ricerca e la Sperimentazione in Agricoltura, Centro di Ricerca per l'Enologia, Asti, Italy Abstract: Wine counterfeiting is an international, multi-billion dollar issue, with some estimates suggesting that up to 5% of wines sold at auctions or secondary markets are fraudulent. Isotope ratio mass spectrometer (IRMS measurements of the 18O/16O stable isotope ratio (δ18O of water-in-wine have been used for wine authentication; however, these analyses are time-consuming and costly. In this preliminary study, off-axis integrated cavity output spectroscopy (OA-ICOS is used to quantify δ18O in wines. This laser-based method has been extensively used to study water isotopes for hydrological and medical applications. Recently, the development of a spectral contaminant identifier (SCI has extended the application of these OA-ICOS analyzers to contaminated water samples (eg, plant, soil, and leaf waters. Here, we utilize OA-ICOS with the SCI to characterize wine samples (9%–15% ethanol, and show that the laser-based instrument provides a δ18O measurement precision of ±0.07‰ (1σ and agrees with IRMS to within ±0.63‰ (1σ. Moreover, by training the SCI on isotopically-characterized wines, the agreement with IRMS improves to within ±0.30‰ (1σ. The utility of the instrument is demonstrated by measuring watered and mixed wines. The method presented here can be readily extended to address other food authentication applications. Keywords: wine isotopes, wine fraud, counterfeit wines, OA-ICOS

Stepwise fluorination - a useful approach for the isotopic analysis of hydrous minerals

Energy Technology Data Exchange (ETDEWEB)

Haimson, M; Knauth, L P [Arizona State Univ., Tempe (USA). Dept. of Geology

1983-09-01

Analytical uncertainties in oxygen isotopic studies of hydrous silica have been investigated using a partial fluorination procedure in which fractional oxygen yields are achieved by reducing the amount of fluorine. Stepwise reaction of opaline silica results in a set of sequential oxygen fractions which show a wide range of delta/sup 18/O values due to variable amounts of water, organic matter, and other impurities. Delta-values for successive fractions in non-biogenic opal systematically increase as water is reacted away and then remain constant to within +- 0.2 per thousand as the remaining silica reacts. Delta-values in biogenic silica increase similarly but then decrease when low /sup 18/O oxide impurities begin to react. The troublesome water component in opal is readily removed by stepwise fluorination. This technique allows more precise oxygen isotope analysis of non-biogenic opal-A, and may improve the analytical precision for biogenic silica and any silicate mineral containing a significant water component.

Tooth Enamel δ13C and δ18O Variations in Modern and Archaeological Horses From Northern Kazakhstan as Indicators of Regional Climate

Science.gov (United States)

Sikora, M. T.; Rosenmeier, M. F.; Stacy, E. M.; Olsen, S. L.

2007-12-01

In this study, the oxygen and carbon isotope values of tooth enamel were measured in forty-one modern and twenty-three Copper Age (3600 - 3100 B.C.) horse specimens from the grassland steppe region of northern Kazakhstan. Modern tooth enamel δ13C and δ18O values were compared with the carbon isotopic compositions of local vegetation and the δ18O values of meteoric waters. Tooth enamel isotope values within the Copper Age specimens (attributed to the so-called Botai culture) were, in turn, compared with modern samples. Average carbon isotopic values within modern bulk tooth enamel samples ranged between -13.7 and -12.0‰ (VPDB). This suggests that the diet of modern northern Kazakhstani horses is comprised almost entirely of C3 plants (considering enamel-diet fractionation factors) consistent with documented grassland compositions within the region. The observed amplitude of δ13C variations within individual teeth (typically less than ~2‰) suggests only minimal seasonal variation in the δ13C of grasses attributed to heat and water stress. Alternatively, the minimal seasonal changes observed within intra-tooth δ13C values may be the direct result of fodder provisioning. Ingested water δ18O values derived from oxygen isotope ratios within bulk tooth enamel samples appear statistically indistinguishable from estimates of regional precipitation, suggesting that Kazakhstani horse tooth enamel δ18O measurements may be used as a direct estimate of the oxygen isotopic composition of meteoric waters. Intra-tooth oxygen isotopic variations therefore reflect the pronounced seasonal variability in precipitation δ18O values tied to temperature changes and amount effects observed annually within Kazakhstan. However, these intra-tooth isotopic variations exhibit slightly reduced amplitudes relative to meteoric water values, suggesting that horses likely consume water from buffered sources such as lakes and wells. Average bulk tooth enamel δ13C values within

δ18O and chemical composition of Libyan Desert Glass, country rocks, and sands: New considerations on target material

Science.gov (United States)

Longinelli, Antonio; Sighinolfi, Giampaolo; de Michele, Vincenzo; Selmo, Enricomaria

2011-02-01

Oxygen isotope and chemical measurements were carried out on 25 samples of Libyan Desert Glass (LDG), 21 samples of sandstone, and 3 of sand from the same area. The δ18O of LDG samples range from 9.0‰ to 11.9‰ (Vienna Standard Mean Ocean Water [VSMOW]); some correlations between isotope data and typological features of the LDG samples are pointed out. The initial δ18O of a bulk parent material may be slightly increased by fusion due to the loss of isotopically light pore water with no isotope exchange with oxygen containing minerals. Accordingly, the δ18O of the bulk parent material of LDG may have been about 9.0 ± 1‰ (VSMOW). The measured bulk sandstone and sand samples have δ18O values ranging from 12.6‰ to 19.5‰ and are consequently ruled out as parent materials, matching the results of previous studies. However, separated quartz fractions have δ18O values compatible with the LDG values suggesting that the modern surface sand inherited quartz from the target material. This hypothesis fits previous findings of lechatelierite and baddeleyite in these materials. As the age of the parent material reported in previous studies is Pan-African, we measured the δ18O values of bulk rock and quartz from intrusives of Pan-African age and the results obtained were compatible with the LDG values. The main element abundances (Fe, Mg, Ca, K, Na) in our LDG samples conform to previous estimates; Fe, Mg, and K tend to be higher in heterogeneous samples with dark layers. The hypothesis of a low-altitude airburst involving silica-rich surface materials deriving from weathered intrusives of Pan-African age, partially melted and blown over a huge surface by supersonic winds matches the results obtained.

Relationships between δ18O in summer precipitation and temperature and moisture trajectories at Muztagata, western China

Institute of Scientific and Technical Information of China (English)

YU; Wusheng; YAO; Tandong; TIAN; Lide; LI; Zhen; SUN; Weizhen; WANG; Yu

2006-01-01

Based on summer observations of stable isotope of precipitation at Muztagata, western China, during 2002―2003, this paper presents the relationship between δ18O in precipitation and air temperature, and discusses the effect of moisture transport on δ18O in precipitation. Results show that air temperature correlates positively with δ18O in precipitation, and the temperature effect controls the δ18O of precipitation in this area. The Muztagata region exhibits high δ18O values in summer precipitation, similar to those shown at stations in adjacent regions. According to the results of our model set up to trace the moisture trajectories, the westerlies and local moisture circulation contribute to variations of oxygen isotopes in precipitation. In addition, the impacts of the moisture transport distance, the moisture transport level, and the incursion of the polar air mass also influence the variations of δ18O in precipitation. The moisture origins and transport mechanisms also contribute to the variation of δ18O in precipitation at Muztagata.

The Benefit of Using Isotopes in NO{sub 3}{sup -} Water Quality Management

Energy Technology Data Exchange (ETDEWEB)

Widory, D. [BRGM, MMA/ISO, Orleans (France)

2013-05-15

Nitrate (NO{sub 3}{sup -}) is one of the world's major pollutants of drinking water resources. Although recent European directives have reduced input from intensive agriculture, NO{sub 3}{sup -} levels in groundwater are dangerously approaching the drinking water limit of 50 mg/L almost everywhere. Determining the sources of groundwater contamination is an important first step towards improving its quality through emission control. It is with this aim that we will review the benefit of using a multi-isotopic approach ({delta}{sup 15}N, {delta}{sup 18}O and {delta}{sup 11}B), in addition to conventional hydrogeological analyses, to trace the origin of NO{sub 3}{sup -} pollution in water. Recent research widely shows the significant added value of using these three isotopes to precisely distinguish nitrate sources, trace them in water and (semi)-quantify their respective contributions. The isotope approach inherently provides more information than classical chemical studies (based mainly on the monitoring of NO{sub 3}{sup -} concentrations), and the technical/economical feasibility of integrating it as part of water body characterization and analysis of pressure and impact due to nitrate pollution, for the more effective implementation of environmental management measures in river basins can be demonstrated to policy makers. (author)

Influence of diet on the distribution of nitrogen isotopes in animals

Energy Technology Data Exchange (ETDEWEB)

DeNiro, M J; Epstein, S [California Inst. of Tech., Pasadena (USA). Div. of Geological Sciences

1981-03-01

The influence of diet on the distribution of nitrogen isotopes in animals was investigated by analyzing animals grown in the laboratory on diets of constant nitrogen isotopic composition. The isotopic composition of the nitrogen in an animal reflects the nitrogen isotopic composition of its diet. The delta/sup 15/N values of the whole bodies of animals are usually more positive than those of their diets. Different individuals of a species raised on the same diet can have significantly different delta/sup 15/N values. The variability of the relationship between the delta/sup 15/N values of animals and their diets is greater for different species raised on the same diet than for the same species raised on different diets. Different tissues of mice are also enriched in /sup 15/N relative to the diet, with the difference between the delta/sup 15/N values of a tissue and the diet depending on both the kind of tissue and the diet involved. The delta/sup 15/N values of collagen and chitin, biochemical components that are often preserved in fossil animal remains, are also related to the delta/sup 15/N value of the diet. The dependence of the delta/sup 15/N values of whole animals and their tissues and biochemical components on the delta/sup 15/N value of diet indicates that the isotopic composition of animal nitrogen can be used to obtain information about an animal's diet if its potential food sources had different delta/sup 15/N values. The isotopic method of dietary analysis was used to reconstruct changes in the diet of the human population that occupied the Tehuacan Valley of Mexico over a 7000 yr span. Variations in the delta/sup 13/C and delta/sup 15/N values of bone collagen suggest that C/sub 4/ and/or CAM plants (presumably mostly corn) and legumes (presumably mostly beans) were introduced into the diet much earlier than suggested by conventional archaeological analysis.

A low-δ18O intrusive breccia from Koegel Fontein, South Africa: Remobilisation of basement that was hydrothermally altered during global glaciation?

Science.gov (United States)

Olianti, Camille A. E.; Harris, Chris

2018-02-01

The Cretaceous Koegel Fontein igneous complex is situated on the west coast of South Africa, and has a high proportion of rocks with abnormally low δ18O values. The rocks with the lowest δ18O values (- 5.2‰) belong to intrusive matrix-supported breccia pipes and dykes, containing a variety of clast types. The breccia rocks range in SiO2 from 44 to 68 wt% and their whole-rock δ18O values vary between - 5.2‰ and + 1.8‰. The major and trace element composition of the breccia rocks is consistent with them containing variable proportions of clasts of Cretaceous intrusive rocks and basement gneiss and the matrix being fluidized material derived from the same source as the clasts. Based on the nature of the clasts contained in the breccia, it was emplaced just prior to intrusion of the main Rietpoort Granite at 134 Ma. All components of the breccia have low δ18O value and, at least in the case of the gneiss clasts, this predates incorporation in the fluidized material. Although the early Cretaceous appears to have been a period of cold climate, it is unlikely that the δ18O values of ambient precipitation ( - 10‰) would have been low enough to have generated the required 18O-depletion. The basement gneiss was probably 2-3 km below the Cretaceous surface, minimizing the possibility of interaction with isotopically unmodified meteoric water, and there is no evidence for foundered blocks of cover rocks in the breccia. There is, therefore, no evidence for downwards movement of material. We favour a model where basement gneiss interacted with extremely 18O-depleted fluid during crustal reworking at 547 Ma, a time of global glaciation. Low-δ18O metamorphic fluids produced by dehydration melting of 18O-depleted gneiss became trapped and, as the fluid pressure increased, failure of the seal resulted in explosive upwards movement of fluidized breccia. Migration was along pre-existing dykes, incorporating fragments of these dykes, as well as the country rock gneiss.

Diagenesis and reservoir quality evolution of palaeocene deep-water, marine sandstones, the Shetland-Faroes Basin, British continental shelf

Energy Technology Data Exchange (ETDEWEB)

Mansurbeg, H. [Department of Earth Sciences, Uppsala University, Villavaegen 16, SE 752 36 Uppsala (Sweden); Morad, S. [Department of Earth Sciences, Uppsala University, Villavaegen 16, SE 752 36 Uppsala (Sweden); Department of Petroleum Geosciences, The Petroleum Institute, P.O. Box 2533, Abu Dhabi (United Arab Emirates); Salem, A. [Faculty of Education at Kafr El-Sheikh, Tanta University, Kafr El-Sheikh (Egypt); Marfil, R.; Caja, M.A. [Departmento Petrologia y Geoquimica, Facultad de Geologia, UCM, 28040 Madrid (Spain); El-ghali, M.A.K. (Geology Department, Al-Fateh University, P.O. Box 13696, Libya); Nystuen, J.P. [Department of Geosciences, University of Oslo, P.O. Box 1047 Blindern, NO-0316 Oslo (Norway); Amorosi, A. [Department of Earth Sciences, University of Bologna, Via Zamboni 67, 40127 Bologna (Italy); Garcia, D. [Centre SPIN, Department GENERIC, Ecole Nationale Superieure des Mines de Saint Etienne 158, Cours Fauriel 42023, Saint-Etienne (France); La Iglesia, A. [Instituto de Geologia Economica (CSIC-UCM), Facultad de Geologia, UCM, 28040 Madrid (Spain)

2008-06-15

The Palaeocene, deep-water marine sandstones recovered from six wells in the Shetland-Faroes Basin represent lowstand, transgressive and highstand systems tract turbiditic sediments. Mineralogic, petrographic, and geochemical analyses of these siliciclastics are used to decipher and discuss the diagenetic alterations and subsequent reservoir quality evolution. The Middle-Upper Palaeocene sandstones (subarkoses to arkoses) from the Shetland-Faroes Basin, British continental shelf are submarine turbiditic deposits that are cemented predominantly by carbonates, quartz and clay minerals. Carbonate cements (intergranular and grain replacive calcite, siderite, ferroan dolomite and ankerite) are of eogenetic and mesogenetic origins. The eogenetic alterations have been mediated by marine, meteoric and mixed marine/meteoric porewaters and resulted mainly in the precipitation of calcite ({delta}{sup 18}O{sub V-PDB}=-10.9 permille and -3.8 permille), trace amounts of non-ferroan dolomite, siderite ({delta}{sup 18}O{sub V-PDB}=-14.4 permille to -0.6 permille), as well as smectite and kaolinite in the lowstand systems tract (LST) and highstand systems tract (HST) turbiditic sandstone below the sequence boundary. Minor eogenetic siderite has precipitated between expanded and kaolinitized micas, primarily biotite. The mesogenetic alterations are interpreted to have been mediated by evolved marine porewaters and resulted in the precipitation of calcite ({delta}{sup 18}O{sub V-PDB}=-12.9 permille to -7.8 permille) and Fe-dolomite/ankerite ({delta}{sup 18}O{sub V-PDB}=-12.1 permille to -6.3 permille) at temperatures of 50-140 and 60-140 C, respectively. Quartz overgrowths and outgrowth, which post- and pre-date the mesogenetic carbonate cements is more common in the LST and TST of distal turbiditic sandstone. Discrete quartz cement, which is closely associated with illite and chlorite, is the final diagenetic phase. The clay minerals include intergranular and grain replacive

Coupled-channel calculation for cross section of fusion and barrier distribution of {}^{16,17,18}O + {}^{16}O reactions

Science.gov (United States)

Fereidonnejad, R.; Sadeghi, H.; Ghambari, M.

2018-03-01

In this work, the effect of multi-phonon excitation on heavy-ion fusion reactions has been studied and fusion barrier distributions of energy intervals near and below the Coulomb barrier have been studied for 16,17,18O + 16O reactions. The structure and deformation of nuclear projectiles have been studied. Given the adaptation of computations to experimental data, our calculations predict the behavior of reactions in intervals of energy in which experimental measurements are not available. In addition the S-factor for these reactions has been calculated. The results showed that the structure and deformation of a nuclear projectile are important factors. The S-factor, obtained in the coupled-channel calculations for the {}^{16}O + {}^{16}O, {}^{17}O +{}^{16}O and {}^{18}O +{}^{16}O reactions, showed good agreement with the experimental data and had a maximum value at an energy near 5, 4.5 and 4 MeV, respectively.

Reference values for fluorine-18-fluorodeoxyglucose and fluorine-18-sodium fluoride uptake in human arteries

DEFF Research Database (Denmark)

Blomberg, Björn A; Thomassen, Anders; de Jong, Pim A

2017-01-01

OBJECTIVE: Reference values of fluorine-18-fluorodeoxyglucose (F-FDG) and fluorine-18-sodium fluoride (F-NaF) uptake in human arteries are unknown. The aim of this study was to determine age-specific and sex-specific reference values of arterial F-FDG and F-NaF uptake. PARTICIPANTS AND METHODS...

Single-molecule magnets: structure and properties of [Mn18O14(O2CMe)18(hep)4(hepH)2(H2O)2](ClO4)2 with spin S = 13.

Science.gov (United States)

Brechin, E K; Sañudo, E C; Wernsdorfer, W; Boskovic, C; Yoo, J; Hendrickson, D N; Yamaguchi, A; Ishimoto, H; Concolino, T E; Rheingold, A L; Christou, G

2005-02-07

The reaction of 2-(hydroxyethyl)pyridine (hepH) with a 2:1 molar mixture of [Mn3O(O2CMe)6(py)3]ClO4 and [Mn3O(O2CMe)6(py)3] in MeCN afforded the new mixed-valent (16Mn(III), 2Mn(II)), octadecanuclear complex [Mn18O14(O2CMe)18(hep)4(hepH)2(H2O)2](ClO4)2 (1) in 20% yield. Complex 1 crystallizes in the triclinic space group P. Direct current magnetic susceptibility studies in a 1.0 T field in the 5.0-300 K range, and variable-temperature variable-field dc magnetization studies in the 2.0-4.0 K and 2.0-5.0 T ranges were obtained on polycrystalline samples. Fitting of magnetization data established that complex 1 possesses a ground-state spin of S = 13 and D = -0.18 K. This was confirmed by the value of the in-phase ac magnetic susceptibility signal. Below 3 K, the complex exhibits a frequency-dependent drop in the in-phase signal, and a concomitant increase in the out-of-phase signal, consistent with slow magnetization relaxation on the ac time scale. This suggests the complex is a single-molecule magnet (SMM), and this was confirmed by hysteresis loops below 1 K in magnetization versus dc field sweeps on a single crystal. Alternating current and direct current magnetization data were combined to yield an Arrhenius plot from which was obtained the effective barrier (U(eff)) for magnetization reversal of 21.3 K. Below 0.2 K, the relaxation becomes temperature-independent, consistent with relaxation only by quantum tunneling of the magnetization (QTM) through the anisotropy barrier via the lowest-energy MS = +/-13 levels of the S = 13 spin manifold. Complex 1 is thus the SMM with the largest ground-state spin to display QTM.

Covariance of oxygen and hydrogen isotopic composition in plant water: Species effects

Energy Technology Data Exchange (ETDEWEB)

Cooper, L.W.; DeNiro, M.J. (Univ. of California, Los Angeles (United States))

1989-12-01

Leaf water becomes enriched in the heavy isotopes of oxygen and hydrogen during evapotranspiration. The magnitude of the enrichment has been shown to be influenced by temperature and humidity, but the effects of species-specific factors on leaf water enrichment of D and {sup 18}O have not been studied for different plants growing together. To learn whether leaf water enrichment patterns and processes for D and {sup 18}O are different for individual species growing under the same environmental conditions the authors tested the proposal that leaf waters in plants with crassulacean acid metabolism (CAM) show high sloped (m in the leaf water equation {delta}D = m {delta}{sup 18}O + b) than in C{sub 3} plants. They determined the relationships between the stable hydrogen ({delta}D) and oxygen ({delta}{sup 18}O) isotope ratios of leaf waters collected during the diurnal cycle of evapotranspiration for Yucca schidigera, Ephedra aspera, Agave deserti, Prunus ilicifolia, Yucca whipplei, Heteromeles arbutifolia, Dyckia fosteriana, Simmondsia chinensis, and Encelia farinosa growing at two sites in southern California. The findings indicate that m in the aforementioned equation is related to the overall residence time for water in the leaf and proportions of water subjected to repeated evapotranspiration enrichments of heavy isotopes.

Isotopic Evolution of Wells in the Geothermal Field of Los Azufres, Michoacan, Mexico; Evolucion isotopica de fluidos de pozos del campo geotermico de Los Azufres, Michoacan, Mexico

Energy Technology Data Exchange (ETDEWEB)

Barragan Reyes, Rosa Maria; Portugal Marin, Enrique; Arellano Gomez, Victor Manel; Aragon Aguilar, Alfonso [Instituto de Investigaciones Electricas (Mexico); Sandoval Medina, Fernando [Comision Federal de Electricidad (Mexico)

2002-12-01

Isotopic ({delta}{sup 1}8 O and {delta}D) data from production and reinjection web fluids from the Los Azufres geothermal field were interpreted in order to define reservoir evolution and the occurrence of physical processes as a result of exploitation. The study included data of 30 wells, which were sampled in September, 2000. General results indicate that different phenomena seem to occur in both zones of the field. In the southern zone there are two different trends of behavior: a mixture of fluids evidenced by the {delta}D versus {delta}{sup 1}8 O trend with a positive slope, was interpreted as the result of reservoir vapor separation at a temperature above 220 Celsius degrees, since for temperatures above 220 Celsius degrees deuterium behaves as a volatile component. No well-defined {delta}{sup D} vs {delta}{sup 1}8 O trend was found for the northern zone, but some points seem to fit the same negative slope trend found in the souther zone. The study of reservoir temperatures estimated by different approaches for particular wells through time, as well as temperature results obtained with a heat and flow well simulator, suggest that reservoir boiling occurs in localized areas in both zone of the field. This process is probably due to exploitation. [Spanish] Se interpretaron datos isotopicos ({delta}{sup 1}8 O y {delta}D) de fluidos de pozos productores y de reinyeccion del campo geotermico de Los Azufres, Michoacan, Mexico, para definir la evolucion del yacimiento y la ocurrencia de procesos fisicos como resultado de la explotacion. En el estudio se consideran datos de treinta pozos segun el muestreo realizado en septiembre de 2000. El estudio de la evolucion en el tiempo de las estimaciones de temperatura de yacimiento mediante diferentes tecnicas, asi como la temperatura obtenida de simulacion de pozos, sugiere que ocurre ebullicion en areas localizadas en ambas zonas del campo debido a la explotacion. Los resultados generales indican la existencia de

Correlation of infrared reflectance ratios at 2.3 microns/1.6 micron and 1.1 micron/1.6 micron with delta O-18 values delineating fossil hydrothermal systems in the Idaho batholith

Science.gov (United States)

Gillespie, A. R.; Criss, R. E.

1983-01-01

Reflectance ratios from laboratory spectra and airborne multispectral images are found to be strongly correlated with delta O-18 values of granite rocks in the Idaho batholith. The correlation is largely a result of interactions between hot water and rock, which lowered the delta O-18 values of the rocks and produced secondary hydrous material. Maps of the ratio of reflectivities at 2.3 and 1.6 microns should delineate fossil hydrothermal systems and provide estimates of alteration intensity. However, hydrous minerals produced during deuteric alteration or weathering cannot be unambiguously distinguished in remotely sensed images from the products of propylitic alteration without the use of narrow-band scanners. The reflectivity at 1.6 micron is strongly correlated with rock density and may be useful in distinguishing rock types in granitic terranes.

Carbon mineralization and pyrite oxidation in groundwater: Importance for silicate weathering in boreal forest soils and stream base-flow chemistry

Energy Technology Data Exchange (ETDEWEB)

Klaminder, J., E-mail: jonatan.klaminder@emg.umu.se [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden)] [Department of Ecology and Environmental Science, Umea University, SE-901 87 (Sweden); Grip, H. [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden); Moerth, C.-M. [Department of Geological Sciences, Stockholm University, 106 91 Stockholm (Sweden); Laudon, H. [Department of Forest Ecology and Management, SLU, SE-901 83 Umea (Sweden)

2011-03-15

Research highlights: {yields} Organic compounds is mineralized during later transport in deep groundwater aquifers. {yields} Carbonic acid generated by this process stimulates dissolution of silicate minerals. {yields} Protons derived from pyrite oxidation also affects weathering in deep groundwater. {yields} The identified weathering mechanisms affect base-flow chemistry in boreal streams. - Abstract: What role does mineralized organic C and sulfide oxidation play in weathering of silicate minerals in deep groundwater aquifers? In this study, how H{sub 2}CO{sub 3}, produced as a result of mineralization of organic matter during groundwater transport, affects silicate weathering in the saturated zone of the mineral soil along a 70 m-long boreal hillslope is demonstrated. Stream water measurements of base cations and {delta}{sup 18}O are included to determine the importance of the deep groundwater system for downstream surface water. The results suggest that H{sub 2}CO{sub 3} generated from organic compounds being mineralized during the lateral transport stimulates weathering at depths between 0.5 and 3 m in the soil. This finding is indicated by progressively increasing concentrations of base cations-, silica- and inorganic C (IC) in the groundwater along the hillslope that co-occur with decreasing organic C (OC) concentrations. Protons derived from sulfide oxidation appear to be an additional driver of the weathering process as indicated by a build-up of SO{sub 4}{sup 2-} in the groundwater during lateral transport and a {delta}{sup 34}S per mille value of +0.26-3.76 per mille in the deep groundwater indicating S inputs from pyrite. The two identified active acids in the deep groundwater are likely to control the base-flow chemistry of streams draining larger catchments (>1 km{sup 2}) as evident by {delta}{sup 18}O signatures and base cation concentrations that overlap with that of the groundwater.

Nitrogen isotope variations in camphor (Cinnamomum Camphora) leaves of different ages in upper and lower canopies as an indicator of atmospheric nitrogen sources

Energy Technology Data Exchange (ETDEWEB)

Xiao Huayun, E-mail: xiaohuayun@vip.skleg.c [State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, No. 46, Guanshui Road, Guiyang 550002 (China); Wu Lianghong; Zhu Renguo; Wang Yanli; Liu Congqiang [State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, No. 46, Guanshui Road, Guiyang 550002 (China)

2011-02-15

Nitrogen isotopic composition of new, middle-aged and old camphor leaves in upper and lower canopies has been determined in a living area, near a motorway and near an industrial area (Jiangan Chemical Fertilizer Plant). We found that at sites near roads, more positive {delta}{sup 15}N values were observed in the camphor leaves, especially in old leaves of upper canopies, and {Delta}{delta}{sup 15}N = {delta}{sup 15}N{sub upper} - {delta}{sup 15}N{sub lower} > 0, while those near the industrial area had more negative {delta}{sup 15}N values and {Delta}{delta}{sup 15}N < 0. These could be explained by two isotopically different atmospheric N sources: greater uptake from isotopically heavy pools of atmospheric NO{sub x} by old leaves in upper canopies at sites adjacent to roads, and greater uptake of {sup 15}N-depleted NH{sub y} in atmospheric deposition by leaves at sites near the industrial area. This study presents novel evidence that {sup 15}N natural abundance of camphor leaves can be used as a robust indicator of atmospheric N sources. - Research highlights: Camphor leaves showed high {delta}{sup 15}N values near roads and low values near the industrial area. The {delta}{sup 15}N values of camphor leaves near roads increased with time of exposure. The {delta}{sup 15}N values of camphor leaves near the industrial area decreased with time of exposure. More positive foliage {delta}{sup 15}N values were found in the upper canopies near roads. Near the industrial area, the upper canopies showed more negative foliage {delta}{sup 15}N values. - Nitrogen isotope in camphor leaves indicating atmospheric nitrogen sources.

A Comparative pO2 Probe and [18F]-Fluoro-Azomycinarabino-Furanoside ([18F]FAZA) PET Study Reveals Anesthesia-Induced Impairment of Oxygenation and Perfusion in Tumor and Muscle.

Science.gov (United States)

Mahling, Moritz; Fuchs, Kerstin; Thaiss, Wolfgang M; Maier, Florian C; Feger, Martina; Bukala, Daniel; Harant, Maren; Eichner, Martin; Reutershan, Jörg; Lang, Florian; Reischl, Gerald; Pichler, Bernd J; Kneilling, Manfred

2015-01-01

CT26 colon carcinoma-bearing mice were anesthetized with isoflurane (IF) or ketamine/xylazine (KX) while breathing air or oxygen (O2). We performed 10 min static PET scans 1 h, 2 h and 3 h after [18F]FAZA injection and calculated the [18F]FAZA-uptake and tumor-to-muscle ratios (T/M). In another experimental group, we placed a pO2 probe in the tumor as well as in the gastrocnemius muscle to measure the pO2 and perfusion. Ketamine/xylazine-anesthetized mice yielded up to 3.5-fold higher T/M-ratios compared to their isoflurane-anesthetized littermates 1 h, 2 h and 3 h after [18F]FAZA injection regardless of whether the mice breathed air or oxygen (3 h, KX-air: 7.1 vs. IF-air: 1.8, p = 0.0001, KX-O2: 4.4 vs. IF-O2: 1.4, p pO2 probe measurements yielded enhanced intra-tumoral pO2 values in air- and oxygen-breathing ketamine/xylazine-anesthetized mice compared to isoflurane-anesthetized mice (KX-air: 1.01 mmHg, IF-air: 0.45 mmHg; KX-O2 9.73 mmHg, IF-O2: 6.25 mmHg). Muscle oxygenation was significantly higher in air-breathing isoflurane-anesthetized (56.9 mmHg) than in ketamine/xylazine-anesthetized mice (33.8 mmHg, p = 0.0003). [18F]FAZA tumor uptake was highest in ketamine/xylazine-anesthetized mice regardless of whether the mice breathed air or oxygen. The generally lower [18F]FAZA whole-body uptake in isoflurane-anesthetized mice could be due to the higher muscle pO2-values in these mice compared to ketamine/xylazine-anesthetized mice. When performing preclinical in vivo hypoxia PET studies, oxygen should be avoided, and ketamine/xylazine-anesthesia might alleviate the identification of tumor hypoxia areals.

Stable isotopic fractionation, climate change and episodic stagnation in the eastern Mediterranean during the late Quaternary

Energy Technology Data Exchange (ETDEWEB)

Vergnaud-Grazzini, C [Laboratoire de Geologie Dynamique, Paris (France); Ryan, W B.F. [Columbia Univ., Palisades, NY (USA). Lamont-Doherty Geological Observatory; Cita, M B [Milan Univ. (Italy)

1977-11-01

Fluctuations in the delta/sup 18/O composition of planktonic foraminifers in eastern Mediterranean piston cores indicate cycles with amplitudes much greater than those which can be attributed alone to global ice-volume changes. Isotopic values become markedly negative within lithostratigraphic levels characterized by the apparition of organic-rich sapropels. These owe their origin to the development of euxinic bottom water during episodes of basin-wide stagnation. The depletion of delta/sup 18/O in many of the sapropels is accompanied by the occurrence of poorly diversified planktonic faunas, and both phenomena are attributed to a strong dilution of the local eastern Mediterranean surface water mass by a combination of glacial run off from large continental ice sheets and by an important increase of regional precipitation synchronous with the transition from pleniglacial to kataglacial climate. Although sapropel accumulation occurs generally during intervals of warming of the Mediterranean region as determined from a quantitative evaluation of planktonic foraminiferal assemblages, the pre-125,000 years, local warming of eastern Mediterranean surface water lagged the acme of glacial melting by up to 15,000 years. Climatic and isotopic cycles are correlative within the eastern Mediterranean for lateral distances in excess of 1000 km and, except for amplitude and phase, they are in most aspects remarkably similar to those recorded in the equatorial Pacific and Caribbean.

Tequila authenticity assessment by headspace SPME-HRGC-IRMS analysis of 13C/12C and 18O/16O ratios of ethanol.

Science.gov (United States)

Aguilar-Cisneros, Blanca O; López, Mercedes G; Richling, Elke; Heckel, Frank; Schreier, Peter

2002-12-18

By use of headspace SPME sampling and a PLOT column, on-line capillary gas chromatography-isotope ratio mass spectrometry was employed in the combustion (C) and the pyrolysis (P) modes (HRGC-C/P-IRMS) to determine the delta(13)C(VPDB) and delta(18)O(VSMOW) values of ethanol in authentic (n = 14) and commercial tequila samples (n = 15) as well as a number of other spirits (n = 23). Whereas with delta(13)C(VPDB) values ranging from -12.1 to -13.2 per thousand and from -12.5 to -14.8 per thousand similar variations were found for 100% agave and mixed tequilas, respectively, the delta(18)O(VSMOW) data differed slightly within these categories: ranges from +22.1 to +22.8 per thousand and +20.8 to +21.7 per thousand were determined for both the authentic 100% agave and mixed products, respectively. The data recorded for commercial tequilas were less homogeneous; delta(13)C(VPDB) data from -10.6 to -13.9 per thousand and delta(18)O(VSMOW) values from +15.5 to +22.7 per thousand were determined in tequilas of both categories. Owing to overlapping data, attempts to differentiate between white, rested, and aged tequilas within each of the two categories failed. In addition, discrimination of tequila samples from other spirits by means of delta(13)C(VPDB) and delta(18)O(VSMOW) data of ethanol was restricted to the products originating from C(3) as well as C(4)/CAM raw materials.

Re-enrichment of O-18 isotopic water used for the production of F-18 in a cyclotron

International Nuclear Information System (INIS)

Kim, J.; Kim, T.S.; Choi, H.; Jang, D.S.; Jeong, D.Y.

2004-01-01

Full text: The demand for and applications of stable isotopes in medicine, industry, and science in the modern era has increased and expanded significantly. Especially, 18 O-enriched water (> 90%) is used as a target in a cyclotron for the production of the β -emitting radioisotope 18 F, which is essential for PET (Positron Emission Tomography) pharmaceutical [ 18 F]-labeled 2-deoxyglucose (FDG) synthesis. Currently, 18 O is produced by a cold distillation of NO (Nitric Oxide) or a fractional distillation of water. These processes, however, are technically complicated and costly so as to limit the production of 18 O. In this regard, it is essential to re-use the used target water as much as possible since the 18 O-enriched water is so expensive (∼ $150/g). In order to recycle the used target water, it is necessary to purify the organic and inorganic impurities contaminated during the 18 f-FDG production loop and to re-enrich the 18 O isotope in the target water diluted during the purification process. For the development of a compact target water 18 O re-enrichment system, the 18 O isotope separation characteristics of MD (Membrane Distillation) were investigated. The 18 O isotopic water permeation and separation characteristics of a hydrophobic PTFE membrane using Air Gap MD and Vacuum Enhanced MD were evaluated. Permeation fluxes were measured by weighing the collected membrane-permeated water vapor. 18 O/ 16 O of each water sample was analyzed by a Tunable Diode Laser Absorption Spectroscopy (TDLAS). We observed the effects of the air in the membrane pores and the temperature gradient applied to the membrane surfaces on the vapor permeation flux and the oxygen isotope separation for the first time. For both AGMD and VEMD, the permeation flux and the degree of 18 O separation increased as the membrane interfacial temperature gradient increased. Even though the oxygen isotope separation and the permeation flux for the VEMD is slightly higher than the AGMD, the

Accurate experimental determination of the isotope effects on the triple point temperature of water. II. Combined dependence on the 18O and 17O abundances

Science.gov (United States)

Faghihi, V.; Kozicki, M.; Aerts-Bijma, A. T.; Jansen, H. G.; Spriensma, J. J.; Peruzzi, A.; Meijer, H. A. J.

2015-12-01

This paper is the second of two articles on the quantification of isotope effects on the triple point temperature of water. In this second article, we address the combined effects of 18O and 17O isotopes. We manufactured five triple point cells with waters with 18O and 17O abundances exceeding widely the natural abundance range while maintaining their natural 18O/17O relationship. The 2H isotopic abundance was kept close to that of VSMOW (Vienna Standard Mean Ocean Water). These cells realized triple point temperatures ranging between  -220 μK to 1420 μK with respect to the temperature realized by a triple point cell filled with VSMOW. Our experiment allowed us to determine an accurate and reliable value for the newly defined combined 18, 17O correction parameter of AO  =  630 μK with a combined uncertainty of 10 μK. To apply this correction, only the 18O abundance of the TPW needs to be known (and the water needs to be of natural origin). Using the results of our two articles, we recommend a correction equation along with the coefficient values for isotopic compositions differing from that of VSMOW and compare the effect of this new equation on a number of triple point cells from the literature and from our own institute. Using our correction equation, the uncertainty in the isotope correction for triple point cell waters used around the world will be  <1 μK.

Controls of precipitation δ18O on the northwestern Tibetan Plateau: A case study at Ngari station

Science.gov (United States)

Guo, Xiaoyu; Tian, Lide; Wen, Rong; Yu, Wusheng; Qu, Dongmei

2017-06-01

The shifting atmospheric circulation between the Indian monsoon and the westerlies on the northwestern Tibetan Plateau (TP) influences precipitation as well as precipitation isotopes. Isotopic records will therefore show historical fluctuations. To understand better the factors controlling present day precipitation δ18O values on the northwestern TP, we made continuous observations of precipitation isotopes at Ngari station from 2010 to 2013. The drivers of precipitation δ18O were investigated using analyses of their statistical relations with temperature, precipitation amount, relative humidity, and convective activities based on outgoing longwave radiation (OLR) data from NOAA satellites, and downward shortwave radiation (DSR) data collected at the Ngari automatic weather station. Atmospheric circulation patterns from NCAR reanalysis, and moisture transport paths of individual events derived from the HYSPLIT model using NCEP data, were also used to trace moisture sources. The results of our study include: (1) The slope and intercept of the Local Meteoric Water Line (LMWL) at Ngari (δD = 8.51 δ18O + 11.57 (R2 = 0.97, p < 0.01)) were higher than for the Global Meteoric Water Line (GMWL), indicating drier local climatic conditions; (2) Precipitation δ18O values showed a weak ;temperature effect; and a weak ;precipitation amount effect; at Ngari; and (3) Convection (or temperature patterns) integrated over several days (0-20) preceding each event were determined to be the main driver of precipitation isotopic values in monsoon (or non-monsoon) season. The longer (shorter) periods of τm days when correlation coefficients between precipitation δ18O and OLR were at their maxima (minima) indicate deep convective activities (shorter moisture transportation pathways) in August (June, July, and September).

Diagenetic conditions of fibrous calcite vein formation in black shales: Petrographic, chemical and isotopic evidence

Energy Technology Data Exchange (ETDEWEB)

Al-Aasm, I.S.; Muir, I. (Imperial Oil Resources, Calgary, AB (Canada)); Morad, S. (Windsor Univ., ON (Canada))

1992-03-01

Antiaxial fibrous calcite veins 2-6 cm thick outcrop parallel to bedding in the Bluefish Member of the Middle Devonian Hare Indian Formation in the Norman Wells area of the Northwest Territories. The Bluefish Member consists of dark brown to black laminated shales with total organic matter content in the 1.8-8.0 wt % range. The basal part of the Member, characterized by the presence of low diversity macrofossils, was deposited under anaerobic conditions on top of the drowned Hume carbonate platform. The pattern of incorporation of host-shale fragments and tiny inclusions into the fibrous calcite indicates repeated episodes of vein opening and sealing. The [delta][sup 13]C values and the low Mn and Fe contents indicate a dominantly marine source of carbonate ions was related to the dissolution of metastable skeletal carbonates in the host shales. The [delta][sup 18]O values suggest precipitation at 30-50[degree]C and burial depths of tens to hundreds of meters. The formation of finely crystalline non-stoichiometric Ca-rich dolomite disseminated in the shale inclusions occurred subsequent to the emplacement of fibrous calcite veins under elevated burial temperatures. 54 refs., 8 figs., 3 tabs.

Sedimentology and geochemistry of carbonates diagenesis. Application to the Malm of the eastern edge of the Paris basin; Sedimentologie et geochimie de la diagenese des carbonates. Application au Malm de la Bordure Est du Bassin de Paris

Energy Technology Data Exchange (ETDEWEB)

Vincent, B

2001-12-01

The important heterogeneity of neritic carbonates reflects: 1 - the facies characteristics of the initial sediments, linked with the diversity of sedimentation environments, and 2 - the post-sedimentation diagenesis characteristics. The aim of this work is to explore this heterogeneity using the {delta}{sup 18}O isotopic signal. A three step pluri-disciplinary approach with different observation scales is established: 1 - a sedimentology study (facies inventory, paleo-environment variations, stratigraphic cycles), 2 - an inventory and chronology of the diagenesis phases and products which have modified he initial sediments, and 3 - a geochemical approach based on the {delta}{sup 18}O signal. This last step combines ionic microprobe measurements performed on separated phases and measurements performed on the whole rock carbonated phase. The carbonate formations under study correspond to the HTM102 borehole made by the ANDRA in the Malm of the eastern edge of the Paris basin. For the stratigraphic approach, some field analogues have been studied (Pagny-sur-Meuse and Gudmont-Villiers sections). (J.S.)

OXYGEN ISOTOPIC COMPOSITIONS OF THE ALLENDE TYPE C CAIs: EVIDENCE FOR ISOTOPIC EXCHANGE DURING NEBULAR MELTING AND ASTEROIDAL THERMAL METAMORPHISM

Energy Technology Data Exchange (ETDEWEB)

Krot, A N; Chaussidon, M; Yurimoto, H; Sakamoto, N; Nagashima, K; Hutcheon, I D; MacPherson, G J

2008-02-21

Based on the mineralogy and petrography, coarse-grained, igneous, anorthite-rich (Type C) calcium-aluminum-rich inclusions (CAIs) in the CV3 carbonaceous chondrite Allende have been recently divided into three groups: (i) CAIs with melilite and Al,Ti-diopside of massive and lacy textures (coarse grains with numerous rounded inclusions of anorthite) in a fine-grained anorthite groundmass (6-1-72, 100, 160), (ii) CAI CG5 with massive melilite, Al,Ti-diopside and anorthite, and (iii) CAIs associated with chondrule material: either containing chondrule fragments in their peripheries (ABC, TS26) or surrounded by chondrule-like, igneous rims (93) (Krot et al., 2007a,b). Here, we report in situ oxygen isotopic measurements of primary (melilite, spinel, Al,Ti-diopside, anorthite) and secondary (grossular, monticellite, forsterite) minerals in these CAIs. Spinel ({Delta}{sup 17}O = -25{per_thousand} to -20{per_thousand}), massive and lacy Al,Ti-diopside ({Delta}{sup 17}O = -20{per_thousand} to -5{per_thousand}) and fine-grained anorthite ({Delta}{sup 17}O = -15{per_thousand} to -2{per_thousand}) in 100, 160 and 6-1-72 are {sup 16}O-enriched relative spinel and coarse-grained Al,Ti-diopside and anorthite in ABC, 93 and TS26 ({Delta}{sup 17}O ranges from -20{per_thousand} to -15{per_thousand}, from -15{per_thousand} to -5{per_thousand}, and from -5{per_thousand} to 0{per_thousand}, respectively). In 6-1-72, massive and lacy Al,Ti-diopside grains are {sup 16}O-depleted ({Delta}{sup 17}O {approx} -13{per_thousand}) relative to spinel ({Delta}{sup 17}O = -23{per_thousand}). Melilite is the most {sup 16}O-depleted mineral in all Allende Type C CAIs. In CAI 100, melilite and secondary grossular, monticellite and forsterite (minerals replacing melilite) are similarly {sup 16}O-depleted, whereas grossular in CAI 160 is {sup 16}O-enriched ({Delta}{sup 17}O = -10{per_thousand} to -6{per_thousand}) relative to melilite ({Delta}{sup 17}O = -5{per_thousand} to -3{per_thousand}). We infer

Alteration of /sup 15/N//sup 14/N and /sup 13/C//sup 12/C ratios of plant matter during the initial stages of diagenesis: studies utilizing archaeological specimens from Peru

Energy Technology Data Exchange (ETDEWEB)

DeNiro, M J [California Univ., Los Angeles (USA). Dept. of Earth and Space Sciences; Hastorf, C A [California Univ., Los Angeles (USA). Dept. of Anthropology

1985-01-01

The stable carbon and nitrogen isotope ratios of plants extracted from Peruvian archaeological sites, ranging in age from 400 to 4000 years B.P., have been measured. The delta/sup 13/C and delta/sup 15/N values of prehistoric plants that were carbonized prior to deposition are similar to those of modern plants which have the same carbon dioxide fixation or nitrogen assimilation mechanisms. In contrast, the delta/sup 15/N values of prehistoric plants that were not carbonized are generally 10 to 20 per mille and as much as 35 per mille more positive than those of their modern counterparts. The delta/sup 13/C and delta/sup 15/N values of different parts of prehistoric uncarbonized plants differ by as much as 8 per mille and 21 per mille respectively, whereas the same parts of modern plants have delta/sup 13/C or delta/sup 15/N values that lie within 2 per mille of one another. SEM analysis eliminated the possibility that diagenetic alteration of the isotope ratios of the prehistoric uncarbonized plants was caused by the adsorption of particulate soil matter. The results are discussed.

Discrimination between ginseng from Korea and China by light stable isotope analysis

Energy Technology Data Exchange (ETDEWEB)

Horacek, Micha, E-mail: micha.horacek@ait.ac.at [Department of Environmental Resources and Technology, Austrian Institute of Technology, 2444 Seibersdorf (Austria); Min, Ji-Sook; Heo, Sang-Cheol [National Institute of Scientific Investigation, 331-1 Shinwol-7dong, Yangcheon-ku, Seoul 158-707 (Korea, Republic of); Soja, Gerhard [Department of Environmental Resources and Technology, Austrian Institute of Technology, 2444 Seibersdorf (Austria)

2010-12-03

Ginseng is a health food and traditional medicine highly valued in Asia. Ginseng from certain origins is higher valued than from other origins, so that a reliable method for differentiation of geographical origin is important for the economics of ginseng production. To discriminate between ginseng samples from South Korea and PR China, 29 samples have been analyzed for the isotopic composition of the elements H, C and N. The results showed {delta}{sup 2}H values between -94 and -79 per mille , for {delta}{sup 13}C -27.9 to -23.7 per mille and for {delta}{sup 15}N 1.3-5.4 per mille for Chinese ginseng. Korean ginseng gave {delta}{sup 2}H ratios between -91 and -69 per mille , {delta}{sup 13}C ratios between -31.2 and -22.4 per mille and {delta}{sup 15}N ratios between -2.4 and +7 per mille . Despite the overlap between the values for individual isotopes, a combination of the isotope systems gave a reasonable differentiation between the two geographic origins. Especially the statistically significant difference in {delta}{sup 2}H ratios facilitated the differentiation between Korean and Chinese ginseng samples.

Determination of wine authenticity and geographical origin by measuring non-exchangeable hydrogen stable isotopes in wine ethanol with EIM-IRMS® methodology in combination with δ18O values obtained from wine water.

Science.gov (United States)

Smajlovic, Ivan; Glavanovic, Mirko; Sparks, Kimberlee L.; Sparks, Jed P.; Jovic, Slobodan

2014-05-01

Wine consumption has grown significantly in the last two decades, with the United States being the leading consumer of wine in the world. It is also the second largest wine producer and importer after the European Union, which consists of 27 European countries. The world has seen a significant increase in production from new world countries, especially the United States, Australia and Chile, and wine imports have grown significantly with this globalization. The quality and authenticity of products have become critical concerns. With the amount of wine being imported the need for verifying wine authenticity and understanding procedures used in wine making has become more important than ever. Understanding the origin of consumed wine in rapidly expanding global economy has become fundamental in order to control quality and protect consumers. In our previous scientific work we have shown that EIM-IRMS®, Ethanol Isotope Measurement - Isotope Ratio Mass Spectrometry (EIM-IRMS®), is capable of providing unique molecular fingerprint that cannot be reproduced or counterfeited. Today we know that δ18O value from the wine water is one of the most important parameters which can give information about wine geographical origin. Earlier we have suggested that grape juice or grape pulp is a closed biochemical system in which all chemical compounds stand in dynamic equilibrium and are in direct connection with each other. Taking that into consideration we have concluded that if system is genuine and if no water, or no sugar has been added to the grape must or grape juice prior to alcoholic fermentation, then ethanol which is made in process of alcoholic fermentation will have specific δD value of non-exchangeable hydrogen stable isotopes which will be in range from -205 to -215 ‰ vs. V-SMOW. In this work we will show that this value, which we named δDn (non-exchangeable hydrogen stable isotopes in ethanol), is very important because it can support or refute conclusions

Thermal evidence of Caledonide foreland, molasse sedimentation in Fennoscandia

Energy Technology Data Exchange (ETDEWEB)

Tullborg, E L; Larsson, S Aa; Bjoerklund, L; Stigh, J [Goeteborg Univ. (Sweden). Dept. of Geology, Earth Sciences Centre; Samuelsson, L [Geological Survey of Sweden, Goeteborg (Sweden). Earth Sciences Centre

1995-11-01

The Phanerozoic rocks present on the Fennoscandian Shield are dominantly of Cambrian to Silurian age. They represent a relatively thin sedimentary cover. The question is: why do we not see any remnants of younger sedimentary rocks? Did they ever exist, have they been eroded, transported and redeposited elsewhere? {delta}{sup 18}O and {delta}{sup 13}C analyses of Ordovician limestones from different places in Sweden and from the Oslo region in Norway show modification of their original marine signature according to the {delta}{sup 18}O concentrations, while the {delta}{sup 13}C concentrations generally are typical for marine limestones. In some cases the modifications can be explained by intrusions of dykes or by metamorphic events, but in most areas the redistribution of the oxygen isotopes indicates burial diagenesis. From a number of published investigations, raised temperatures at the present surface during the late Palaeozoic, are indicated by different temperature indicators. We suggest that these increased temperatures were due to a sedimentary cover of mainly Devonian sediments deposited on top of the Cambrian-Silurian sequence. This palaeo-cover caused raised temperatures at the present rock surface. In the Proterozoic basement, annealing of fission tracks in apatite and mobility of radiogenic lead also give evidence of increased temperatures. A model where the thickness of the Upper Paleozoic cover of the Caledonian foreland is 2-4 kilometers thick is suggested. This cover mainly consisted of late Silurian-Devonian erosion products from the Caledonides, the latter formed during a Silurian continent-continent collision. A major Permian to Triassic uplift and erosion reduced the cover significantly. 94 refs, 9 figs.

A Pliocene marine diatom δ18O record of terrestrial-marine feedbacks and orbitally-paced cryogenic brine formation in the McMurdo Dry Valleys

Science.gov (United States)

Dodd, J. P.; Abbott, T.; Gibbons, J. A.

2017-12-01

Orbital frequencies are well documented in a number of terrestrial and marine climate records throughout the Cenozoic; however, assessing the feedbacks and timing of terrestrial-marine systems on glacial-interglacial timescales is often challenging. This is particularly the case in high-latitude, near-shore environments where traditional proxy records like benthic foraminifera are absent. Here we present oxygen isotope (δ18O and δ17O) values from marine diatom silica in the mid-Pliocene (3.5 - 4.7Ma) section of the AND-1B core from McMurdo Sound, Antarctica. Diatom silica δ18O values range between +28.1 and +36.4‰ VSMOW. Over a range of temperatures (0 to 10°C) that reflect both growth and shallow (fall on a mixing line between marine and meteoric waters, which also supports our cryogenic brine hypothesis. The AND-1B δ18O values have an inverse relationship with the stacked benthic foraminifera δ18O record where lower δ18O values in the AND-1B diatom silica correspond with colder intervals, and we interpret variations in the diatom δ18O values as increased brine flux from the MDV to McMurdo Sound. Currently, subsurface brines in the MDV are hydrologically connected with McMurdo Sound. Density-driven transport of these brines from the MDV to the marine costal environments during the warm mid-Pliocene indicate a potentially overlooked terrestrial source of hypersaline waters. Although the lateral extent of these brines is not known, mixing between the terrestrial cryogenic brines and seawater may represent a significant flux of hypersaline water to the marine environment during warmer-than-present global conditions.

Role of crude oil in the genesis of Mississippi Valley-type deposits. Evidence from the Cincinnati arch

Energy Technology Data Exchange (ETDEWEB)

Kesler, S.E.; Jones, H.D. (Univ. of Michigan, Ann Arbor, MI (United States)); Furman, F.C. (Univ. of Missouri, Rolla, MO (United States)); Sassen, R. (Texas A M Univ., College Station, TX (United States)); Anderson, W.H. (Univ. of Kentucky, Lexington, KY (United States)); Kyle, J.R. (Univ. of Texas, Austin, TX (United States))

1994-07-01

Mississippi Valley-type (MVT) sulfide minerals and oil from deposits along the Cincinnati arch have almost identical [delta][sup 34]S values (-9% to +9% for MVT sulfides, -12% to +9% for oils). These values are very similar to those for MVT sulfides and oil in the Illinois-Kentucky district and support their proposed inclusion in a regional hydrothermal system. Many MVT deposits with low [delta][sup 34]S values are closely associated with oil, whereas MVT deposits with high [delta][sup 34]S values often contain bitumen. Reduced sulfur in MVT deposits with high [delta][sup 34]S values probably came from thermochemical sulfate reduction, whereas that in MVT deposits with low [delta][sup 34]S values probably came from oil and related organic matter. Oil-related sulfur could have been derived from oil fields or disseminated oil and other organic matter in regional wallrocks. 44 refs., 3 figs., 2 tabs.

Study of some excited states in 21Ne-21Na, 18O-18F and 15N-15O nuclei

International Nuclear Information System (INIS)

Drain, D.

1977-01-01

The study of 21 Ne- 21 Na, 18 O- 18 F and 15 N- 15 O nuclei was performed through proton capture and transfer reactions and allows to determine the spins and parities of some excited states, give the gamma deexcitation schemes of these levels, compute the neutron and proton reduced width γ 2 sub(n) and γ 2 sub(p). The levels studied are: in 21 Na 4.15 20 Ne(p,p), (p,p'), (p,p'γ) and (pγ) reactions) and in 21 Ne: E(exc)=4.73, 5.69 and 5.78 MeV ( 20 Ne (p,p) reaction); in 18 O: E(exc) 17 O(d,p) reaction); in 15 O: 8.92 MeV doublet and 8.98 MeV level (angular correlation 14 N(p,γγ) and in 15 N: 9.05 14 N(d,p) reaction). A comparison with theoretical results is discussed and analog states are pointed out [fr

A modern Sr/Ca-δ18O-sea surface temperature calibration for Isopora corals on the Great Barrier Reef

Science.gov (United States)

Brenner, Logan D.; Linsley, Braddock K.; Potts, Donald C.

2017-02-01

Isopora (Acroporidae) is a genus of often encrusting, branching to submassive corals that are common in many shallow habitats on modern and fossil Indo-West Pacific reefs. Although abundant, Isopora is largely absent from paleoceanographic literature. The scarcity of large Porites and the abundance of Isopora retrieved from the Great Barrier Reef (GBR) on Integrated Ocean Drilling Program Expedition 325 focused paleoceanographic attention on Isopora. Here we provide the first independent high-resolution calibration of both Sr/Ca and δ18O for temperature analyses based on Isopora and demonstrate its consistency with Porites records. We developed modern skeletal Sr/Ca- and δ18O-sea surface temperature (SST) calibrations based on five modern Isopora colonies from Heron Island in the southern GBR. Pairing the coral Sr/Ca record with monthly SST data yielded Sr/Ca-SST sensitivities from -0.061 ± 0.004 (centered) to -0.083 ± 0.007 (raw) mmol/mol °C-1 based on reduced major axis regressions. These sensitivities are in the middle of the range of published Porites values and overlap most published values for Isopora, -0.075 ± 0.011 to -0.065 ± 0.011 mmol/mol °C-1. The δ18O-SST sensitivities range from -0.184 ± 0.014 (centered) to -0.185 ± 0.014 (raw) ‰ °C-1, assuming that all seasonal variation in δ18O was due to SST. These δ18O-SST sensitivities are smaller than the widely accepted value of -0.23‰ °C-1 for biogenic aragonite but are at the upper end of high-resolution Porites-defined sensitivities that are consistently less than the aforementioned established value. Our results validate the use of Isopora as an alternative source of paleoceanographic records in habitats where large massive Porites are scarce or absent.

Initial isotopic geochemistry ({delta} 18 O, {delta} D) of fluids from wells of the Los Humeros, Pue., geothermal field; Geoquimica isotopica ({delta} 18 O, {delta} D) inicial de fluidos de pozos del campo geotermico de Los Humeros, Pue.

Energy Technology Data Exchange (ETDEWEB)

Barragan Reyes, Rosa Maria; Arellano Gomez, Victor Manuel [Instituto de Investigaciones Electricas, Gerencia de Geotermia, Cuernavaca, Morelos (Mexico)]. E-mail: rmb@iie.org.mx; Ramirez Montes, Miguel; Tovar Aguado, Rigoberto [Comision Federal de Electricidad, Gerencia de Proyectos Geotermoelectricos, Morelia, Michoacan (Mexico)

2010-01-15

Isotopic data ({delta} 18 O, {delta} D) from fluids from production wells at the Los Humeros, Pue., geothermal field were analyzed to investigate the possible origin of these fluids and the dominant processes of the reservoir at its initial state. According to pre-exploitation data, it is suggested the Los Humeros reservoir fluids are made of a mixture of meteoric water of very light isotopic composition (paleo-fluids) and andesitic water. The relationship {delta} D vs {delta} 18 O from pre-exploitation data indicates the produced fluids are composed of a mixture of (at least) two fluids with distinct isotopic compositions. At the more enriched end of the mixing relationship are the isotopic compositions of the wells H-23 and H-18 (located in the southern area of the field), while the lighter fluids were found in well H-16 (originally) and then in well H-16 (repaired). It was found that the liquid phases of deep wells are more enriched in {delta} 18 O while the shallow wells present lower values, suggesting a convection process at the initial state. Based on this isotopic profile, it is considered that even the production depths of the wells H-1, H-12 and H-16 (repaired) are just about the same, but their respective isotopic compositions are quite different. The {delta} 18 O value for well H-16 (repaired) seems to be that of condensate steam, while the corresponding values for wells H-1 and H-12 fall within the value interval of the deep wells (H-23). This suggests wells H-1 and H-12 are collecting very deep fluids enriched in {delta} 18 O. These results could be useful in creating a conceptual model of the reservoir. [Spanish] Se analizaron datos isotopicos ({delta}18 O, {delta}D) de los fluidos de pozos productores del campo geotermico de Los Humeros, Pue., para investigar el posible origen de los fluidos asi como los procesos dominantes del yacimiento en su estado inicial. De acuerdo con datos previos a la explotacion, se plantea que los fluidos del yacimiento

Use of the isotope flux ratio approach to investigate the C18O16O and 13CO2 exchange near the floor of a temperate deciduous forest

Directory of Open Access Journals (Sweden)

P. Bartlett

2012-07-01

Full Text Available Stable isotopologues of CO2, such as 13CO2 and C18OO, have been used to study the CO2 exchange between land and atmosphere. The advent of new measuring techniques has allowed near-continuous measurements of stable isotopes in the air. These measurements can be used with micrometeorological techniques, providing new tools to investigate the isotope exchange in ecosystems. The objectives of this study were to evaluate the use of the isotope flux ratio method (IFR near the forest floor of a temperate deciduous forest and to study the temporal dynamics of δ18O of CO2 flux near the forest floor by comparing IFR estimates with estimates of δ18O of net soil CO2 flux provided by an analytical model. Mixing ratios of 12C16O2, 13CO2 and C16O18O were measured within and above a temperate deciduous forest, using the tunable diode laser spectroscopy technique. The half-hourly compositions of the CO2 flux near the forest floor (δ13CF and δ18OF were calculated by IFR and compared with estimates provided by a modified Keeling plot technique (mKP and by a Lagrangian dispersion analysis (WT analysis. The mKP and IFR δ18OF estimates showed good agreement (slope = 1.03 and correlation, R2 = 0.80. The δ13CF estimates from the two methods varied in a narrow range of −32.7 and −23‰; the mean (± SE mKP and IFR δ13CF values were −27.5‰ (±0.2 and −27.3‰ (±0.1, respectively, and were statistically identical (p>0.05. WT analysis and IFR δ18OF estimates showed better correlation (R2 = 0.37 when only turbulent periods (u*>0.6 m s−1 were included in the analysis. The large amount of data captured (~95 % of half-hour periods evaluated for the IFR in comparison with mKP (27 % shows that the former provides new opportunities for studying δ18OF dynamics within forest canopies. Values of δ18OF showed large temporal variation, with values ranging from −31.4‰ (DOY 208 to −11.2‰ (DOY 221. Precipitation events caused substantial variation (~8�

The synthesis of 8-β-[(methylsulfinyl-[18O])-methyl]-6-propylergoline

International Nuclear Information System (INIS)

Wheeler, W.J.

1987-01-01

The synthesis of 18 O-labeled 8-Β-[(methylsulfinyl)-methyl]-6-propyl-ergoline(pergolide-[ 18 O]-sulfoxide) of undetermined stereochemistry by the reaction of 8-Β-(methylthiomethyl)-6-propyl-ergoline (pergolide) with bis-(4-methoxyphenyl)-selen-[ 18 O]-oxide in acetic acid is described. Although the yields were low and the incorporation of 18 O was not high, this procedure represents a convenient method for the preparation of 18 O-labeled sulfoxides of pergolide and other sulfides present in compounds for which the usual methods are inappropriate. (author)

Boron/calcium ratios in Globigerinoides ruber from the Arabian Sea: Implications for controls on boron incorporation

Digital Repository Service at National Institute of Oceanography (India)

Naik, S.S.; Naidu, P.D.

of Globigerinoides ruber from the Ocean Drilling Program (ODP) Site 723A (western Arabian Sea) and Core AAS9/21 (eastern Arabian Sea) from the last 22 kyr were analysed for B/Ca, delta>18O and Mg/Ca. B/Ca was compared to reconstructed salinity and sea...

Continental-Scale Patterns in Modern Wood Cellulose δ18O: Implications for Interpreting Paleo-Wood δ18O

Science.gov (United States)

Richter, S. L.; Johnson, A. H.; Dranoff, M. M.; Taylor, K. D.

2006-05-01

Ancient wood from Siberia and Arctic Canada is readily available and spans > 40 my of changing climate. Its isotopic composition might provide useful climate information, but there are several uncertainties that must be considered when interpreting the analyzed values of this potential resource. Aside from possible problems associated with diagenetic changes, oxygen isotopes in wood cellulose (δ18Ocel) are not likely to be good paleothermometers for the distant past when global patterns of precipitation δ18O (δ18Oppt) and temperatures were different, nor might they be good predictors of δ18Oppt because paleo-relative humidity, a contributor to δ18Ocel, is difficult to quantify. We sampled naturally growing, predominantly native trees in forested regions of North American and the Caribbean to determine how applicable the established relationships among δ18Ocel, temperature, relative humidity and δ18Oppt were at the continental scale, and how much relative humidity modifies the δ18Oppt signal. Different species at the same site may or may not have access to groundwater; they may have different phenological and physiological constraints that could cause them to have different δ18Ocel. Accordingly, we assessed species composition and depth to water table as potential sources of variability in δ18Ocel. We found up to 4‰ differences among species growing at the same site with conifer cellulose more enriched than angiosperm cellulose by 1.5‰ (P<.00001). Differences in landscape position, reflecting differing access to the water table, produced small (1‰) differences in δ18Ocel. While δ18Ocel was correlated with MAT (R2=.83-.91, P<.001), average summer minimum relative humidity (RH) combined with δ18Oppt explained most of the variability (R=.96) in δ18Ocel across North American and Caribbean forests. The isotopic enrichment that occurs during the processes leading to the incorporation of precipitation oxygen in cellulose is not constant, but varies from

Olivine in Martian Meteorite Allan Hills 84001: Evidence for a High-Temperature Origin and Implications for Signs of Life

Science.gov (United States)

Shearer, C. K.; Leshin, L. A.; Adcock, C. T.

1999-01-01

Olivine from Martian meteorite Allan Hills (ALH) 84001 occurs as clusters within orthopyroxene adjacent to fractures containing disrupted carbonate globules and feldspathic shock glass. The inclusions are irregular in shape and range in size from approx. 40 microns to submicrometer. Some of the inclusions are elongate and boudinage-like. The olivine grains are in sharp contact with the enclosing orthopyroxene and often contain small inclusions of chromite The olivine exhibits a very limited range of composition from Fo(sub 65) to Fo(sub 66) (n = 25). The delta(sup 18)O values of the olivine and orthopyroxene analyzed by ion microprobe range from +4.3 to +5.3% and are indistinguishable from each other within analytical uncertainty. The mineral chemistries, O-isotopic data, and textural relationships indicate that the olivine inclusions were produced at a temperature greater than 800 C. It is unlikely that the olivines formed during the same event that gave rise to the carbonates in ALH 84001, which have more elevated and variable delta(sup 18)O values, and were probably formed from fluids that were not in isotopic equilibrium with the orthopyroxene or olivine The reactions most likely instrumental in the formation of olivine could be either the dehydration of hydrous silicates that formed during carbonate precipitation or the reduction of orthopyroxene and spinel If the olivine was formed by either reaction during a postcarbonate beating event, the implications are profound with regards to the interpretations of McKay et al. Due to the low diffusion rates in carbonates, this rapid, high-temperature event would have resulted in the preservation of the fine-scale carbonate zoning' while partially devolatilizing select carbonate compositions on a submicrometer scale. This may have resulted in the formation of the minute magnetite grains that McKay et al attributed to biogenic activity.

Nitrogen fertilization and δ18 O of CO2 have no effect on 18 O-enrichment of leaf water and cellulose in Cleistogenes squarrosa (C4 ) - is VPD the sole control?

Science.gov (United States)

Liu, Hai Tao; Gong, Xiao Ying; Schäufele, Rudi; Yang, Fang; Hirl, Regina Theresia; Schmidt, Anja; Schnyder, Hans

2016-12-01

The oxygen isotope composition of cellulose (δ 18 O Cel ) archives hydrological and physiological information. Here, we assess previously unexplored direct and interactive effects of the δ 18 O of CO 2 (δ 18 O CO2 ), nitrogen (N) fertilizer supply and vapour pressure deficit (VPD) on δ 18 O Cel , 18 O-enrichment of leaf water (Δ 18 O LW ) and cellulose (Δ 18 O Cel ) relative to source water, and p ex p x , the proportion of oxygen in cellulose that exchanged with unenriched water at the site of cellulose synthesis, in a C 4 grass (Cleistogenes squarrosa). δ 18 O CO2 and N supply, and their interactions with VPD, had no effect on δ 18 O Cel , Δ 18 O LW , Δ 18 O Cel and p ex p x . Δ 18 O Cel and Δ 18 O LW increased with VPD, while p ex p x decreased. That VPD-effect on p ex p x was supported by sensitivity tests to variation of Δ 18 O LW and the equilibrium fractionation factor between carbonyl oxygen and water. N supply altered growth and morphological features, but not 18 O relations; conversely, VPD had no effect on growth or morphology, but controlled 18 O relations. The work implies that reconstructions of VPD from Δ 18 O Cel would overestimate amplitudes of VPD variation, at least in this species, if the VPD-effect on p ex p x is ignored. Progress in understanding the relationship between Δ 18 O LW and Δ 18 O Cel will require separate investigations of p ex and p x and of their responses to environmental conditions. © 2016 John Wiley & Sons Ltd.

Prognostic value of tumour blood flow, [18F]EF5 and [18F]FDG PET/CT imaging in patients with head and neck cancer treated with radiochemotherapy

International Nuclear Information System (INIS)

Komar, Gaber; Eskola, Olli; Sipilae, Hannu; Solin, Olof; Lehtioe, Kaisa; Levola, Helena; Lindholm, Paula; Seppaelae, Jan; Seppaenen, Marko; Grenman, Reidar; Minn, Heikki

2014-01-01

In order to improve the treatment of squamous cell carcinoma of the head and neck, precise information on the treated tumour's biology is required and the prognostic importance of different biological parameters needs to be determined. The aim of our study was to determine the predictive value of pretreatment PET/CT imaging using [ 18 F]FDG, a new hypoxia tracer [ 18 F]EF5 and the perfusion tracer [ 15 O]H 2 O in patients with squamous cell cancer of the head and neck treated with radiochemotherapy. The study group comprised 22 patients with confirmed squamous cell carcinoma of the head and neck who underwent a PET/CT scan using the above tracers before any treatment. Patients were later treated with a combination of radiochemotherapy and surgery. Parametric blood flow was calculated from dynamic [ 15 O]H 2 O PET images using a one-tissue compartment model. [ 18 F]FDG images were analysed by calculating standardized uptake values (SUV) and metabolically active tumour volumes (MATV). [ 18 F]EF5 images were analysed by calculating tumour-to-muscle uptake ratios (T/M ratio). A T/M ratio of 1.5 was considered a significant threshold and used to determine tumour hypoxic subvolumes (HS) and hypoxic fraction area. The findings were finally correlated with the pretreatment clinical findings (overall stage and TNM stage) as well as the outcome following radiochemotherapy in terms of local control and overall patient survival. Tumour stage and T-classification did not show any significant differences in comparison to the patients' metabolic and functional characteristics measured on PET. Using the Cox proportional hazards model, a shorter overall survival was associated with MATV (p = 0.008, HR = 1.108), maximum [ 18 F]EF5 T/M ratio (p = 0.0145, HR = 4.084) and tumour HS (p = 0.0047, HR = 1.112). None of the PET parameters showed a significant effect on patient survival in the log-rank test, although [ 18 F]EF5 maximum T/M ratio was the closest (p = 0.109). By contrast

The influence of clouds and diffuse radiation on ecosystem-atmosphere CO2 and CO18O exhanges

Energy Technology Data Exchange (ETDEWEB)

Still, C.J.; Riley, W.J.; Biraud, S.C.; Noone, D.C.; Buenning, N.H.; Randerson, J.T.; Torn, M.S.; Welker, J.; White, J.W.C.; Vachon, R.; Farquhar, G.D.; Berry, J.A.

2009-05-01

This study evaluates the potential impact of clouds on ecosystem CO{sub 2} and CO{sub 2} isotope fluxes ('isofluxes') in two contrasting ecosystems (a broadleaf deciduous forest and a C{sub 4} grassland), in a region for which cloud cover, meteorological, and isotope data are available for driving the isotope-enabled land surface model, ISOLSM. Our model results indicate a large impact of clouds on ecosystem CO{sub 2} fluxes and isofluxes. Despite lower irradiance on partly cloudy and cloudy days, predicted forest canopy photosynthesis was substantially higher than on clear, sunny days, and the highest carbon uptake was achieved on the cloudiest day. This effect was driven by a large increase in light-limited shade leaf photosynthesis following an increase in the diffuse fraction of irradiance. Photosynthetic isofluxes, by contrast, were largest on partly cloudy days, as leaf water isotopic composition was only slightly depleted and photosynthesis was enhanced, as compared to adjacent clear sky days. On the cloudiest day, the forest exhibited intermediate isofluxes: although photosynthesis was highest on this day, leaf-to-atmosphere isofluxes were reduced from a feedback of transpiration on canopy relative humidity and leaf water. Photosynthesis and isofluxes were both reduced in the C{sub 4} grass canopy with increasing cloud cover and diffuse fraction as a result of near-constant light limitation of photosynthesis. These results suggest that some of the unexplained variation in global mean {delta}{sup 18}O of CO{sub 2} may be driven by large-scale changes in clouds and aerosols and their impacts on diffuse radiation, photosynthesis, and relative humidity.

Determination of 18O concentrations in microsamples of biological fluids

International Nuclear Information System (INIS)

Cohen, D.D.; Bradshaw, S.D.; Bradshaw, F.J.

1990-01-01

The 18 O(p, α) 15 N reaction has been developed for the analysis of microsamples of biological fluids containing 18 O-enriched water. Samples as small as 50 μl have been used. Well characterized Ta 2 O 5 targets were prepared from these fluids and irradiated with several hundred nA of protons from the 3 MV Van de Graaff at Lucas Heights. The broad (47 keV) 846 kV resonance in this reaction was used to measure 18 O concentrations down to natural backgrounds (0.2 at.%) in a few minutes of accelerator running time. Concentrations of 18 O from 0 to 5 at.% were measured in body fluids in small Australian lizards directly after doping with 18 O-enriched water and then again after several days of roaming around in their natural desert environments. The changes in these levels were related to the metabolic rates of these animals. (orig.)

Diagenetic modification of Knox evaporative-dolomite geochemistry by middle Ordovician paleoaquifer/burial fluids

Energy Technology Data Exchange (ETDEWEB)

Montanez, I.P.; Read, J.F.

1986-05-01

Early Ordovician upper Knox cyclic carbonates (100,000-year periods) were deposited on a ramp in a semiarid setting. Inner ramp facies are completely dolomitized, whereas only cycle caps on the outer ramp are dolomite. Laminite caps on leading edges of prograding flats were dolomitized by evaporative, storm-recharged marine waters that precipitated CoCO/sub 3/ and minor amounts of CaSO/sub 4/. Subtidal facies beneath interiors of supratidal flats (up to 200 km wide)were dolomitized by shallow subsurface brines as the flats prograded. Inner ramp areas existed as supretidal flats for as long as 100,000 years, hence only there are sequences completely dolomitized. Tidal-flat dolomites consist of euhedral to subhedral fabric preservation mosaics (crystals 5-50 ..mu..m, and up to 300 ..mu..m in replaced pelletal layers). Dolomitized subtidal sediments are composed of 20-200 ..mu..m dolomite crystals. Most of the early dolomites are fabric retentive initially, becoming more fabric destructive with increasing exposure to dolomitizing fluids. Fe values are up to 2000 ppm, and Mn values are up to 500 ppm. delta/sup 18/O values show strong geographic control, with samples depleted (up to - 7 per thousand) relative to pristine evaporative dolomites derived from concentrated Ordovician seawater. Burial dolomites are enriched in Fe (up to 14,000 ppm) and depleted in delta/sup 18/O, suggesting precipitation from basinal brines at elevated temperatures. Geochemical data suggest that evaporative dolomites have undergone modification by isotopically lighter fluids. Alteration most likely occurred within a Middle Ordovician meteoric aquifer system or less likely by later Paleozoic basinal brines. Regional geologic data for Knox Group carbonates throughout the eastern US are vital in constraining dolomitization models.

Gridding Global δ 18Owater and Interpreting Core Top δ 18Oforam

Science.gov (United States)

Legrande, A. N.; Schmidt, G.

2004-05-01

Estimations of the oxygen isotope ratio in seawater (δ 18O water) traditionally have relied on regional δ 18O water to salinity relationships to convert seawater salinity into δ 18O water. This indirect method of determining δ 18O water is necessary since ?18Owater measurements are relatively sparse. We improve upon this process by constructing local δ 18O water to salinity curves using the Schmidt et al. (1999) global database of δ 18O water and salinity. We calculate local δ 18O water to salinity relationship on a 1x1 grid based on the closest database points to each grid box. Each ocean basin is analyzed separately, and each curve is processed to exclude outliers. These local relationships in combination with seawater salinity (Levitus, 1994) allow us to construct a global map of δ 18O water on a 1x1 grid. We combine seawater temperature (Levitus, 1994) with this dataset to predict δ 18O calcite on a 1x1 grid. These predicted values are then compared to previous compilations of core top δ 18O foram data for individual species of foraminifera. This comparison provides insight into the calcification habitats (as inferred by seawater temperature and salinity) of these species. Additionally, we compare the 1x1 grid of δ 18O water to preliminary output from the latest GISS coupled Atmosphere/Ocean GCM that tracks water isotopes through the hydrologic cycle. This comparison provides insight into possible model applications as a tool to aid in interpreting paleo-isotope data.

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.

Assessment of Groundwater Quality in the Western Aquifers of Mauritius Using Isotope Techniques

Energy Technology Data Exchange (ETDEWEB)

Dindyal, D.; Brizmohun, R.; Fanny, J. O.Y. [National Environmental Laboratory, Reduit (Mauritius); Sacchi, E. [Dipartimento di Scienze della Terra e dell' Ambiente, Universita di Pavia (Italy)

2013-07-15

This contribution reports the results obtained in the IAEA TC project Mar/8/007, initiated in 2007. Fourteen boreholes were sampled during three sampling campaigns (rainy season, winter and summer): analyses include major ions, trace elements, stable isotopes ({delta}{sup 2}H, {delta}{sup 18}O and {delta}{sup 13}C) and a microbiological assessment (TC and E. coli). Results indicate that groundwater quality is generally good. Recharge mostly occurs in the central plateau area, but the increase in nitrates along the groundwater flow and the common presence of E. coli indicate that a minor recharge occurs all over the aquifer's extension. Infiltration is rapid and favoured by the presence of vertical fractures in the basalts. Discharge occurs at a lower altitude and is marked by a different stable isotope content and lower nitrates. In addition to validating the general groundwater circulation model, these results show that aquifers are not adequately protected against a possible input of pollutants from the surface. (author)

Nuclear microanalysis of 16O and 18O in near-surface regions of solids. Applications

International Nuclear Information System (INIS)

Amsel, G.

The best suited nuclear technique for 18 O analysis is the direct observation of nuclear reactions. Here, instead of measuring an induced radioactivity, one observes the particles emitted as a result of the O 18 (p,α)N 15 reaction. The α particles which are produced may be detected with surface barrier semiconductor detectors; they present unit detection efficiency and allow one to realize large solid angles of detection, while their energy resolution is excellent. For getting O 18 /O 16 ratios, 16 O must also be measured. This is achieved in a similar way, using the O 16 (d,p) 17 O reaction [fr

Reconstructing the δ(18) O of atmospheric water vapour via the CAM epiphyte Tillandsia usneoides: seasonal controls on δ(18) O in the field and large-scale reconstruction of δ(18) Oa.

Science.gov (United States)

Helliker, Brent R

2014-03-01

Using both oxygen isotope ratios of leaf water (δ(18) OL ) and cellulose (δ(18) OC ) of Tillandsia usneoides in situ, this paper examined how short- and long-term responses to environmental variation and model parameterization affected the reconstruction of the atmospheric water vapour (δ(18) Oa ). During sample-intensive field campaigns, predictions of δ(18) OL matched observations well using a non-steady-state model, but the model required data-rich parameterization. Predictions from the more easily parameterized maximum enrichment model (δ(18) OL-M ) matched observed δ(18) OL and observed δ(18) Oa when leaf water turnover was less than 3.5 d. Using the δ(18) OL-M model and weekly samples of δ(18) OL across two growing seasons in Florida, USA, reconstructed δ(18) Oa was -12.6 ± 0.3‰. This is compared with δ(18) Oa of -12.4 ± 0.2‰ resolved from the growing-season-weighted δ(18) OC . Both of these values were similar to δ(18) Oa in equilibrium with precipitation, -12.9‰. δ(18) Oa was also reconstructed through a large-scale transect with δ(18) OL and the growing-season-integrated δ(18) OC across the southeastern United States. There was considerable large-scale variation, but there was regional, weather-induced coherence in δ(18) Oa when using δ(18) OL . The reconstruction of δ(18) Oa with δ(18) OC generally supported the assumption of δ(18) Oa being in equilibrium with precipitation δ(18) O (δ(18) Oppt ), but the pool of δ(18) Oppt with which δ(18) Oa was in equilibrium - growing season versus annual δ(18) Oppt - changed with latitude. © 2013 John Wiley & Sons Ltd.

Test and implementation of position sensors on load and unload [18O]H2O control valve of the target used in 18F - production by proton irradiation

International Nuclear Information System (INIS)

Costa, Osvaldo L. da; Sciani, Valdir

2009-01-01

The radionuclide 18 F used to produce the radiopharmaceutical [ 18 F]FDG has 109.7 min of half-life, becoming your productive chain so peculiar, because since the beginning of [ 18 O]H 2 O irradiation until the PET-CT exam there is a period about six hours, and any procedure fail in the productive chain will result in a delay to the PET CT exam. The absence of the position signs from [ 18 O]H 2 O load and unload valve of the target may result in 18 F production loss and even area contamination around the target. In this paper, three types of position sensors, into cyclotron radionuclides production environment in Cyclotron Accelerator Center from IPEN-CNEN/SP were tested. The tests were an indicative to discover the fitter sensor to the [ 18 O]H 2 O load and unload valve from target used in [ 18 F]fluoride production. After finding the fitter sensor, it was implemented in 18 F- target, supplying the correct position from [ 18 O]H 2 O load and unload valve to programmable logic controller, that had the software modified, respecting in this way the valve position. By this way, it was possible to reduce the incidence of fails, increasing the reliability in [ 18 F]FDG productive chain. (author)

Technical report on analysis and purification of used O-18 cyclotron target water

International Nuclear Information System (INIS)

Kim, T. S.; Jeong, D. Y.; Kim, J. W.; Ko, K. H.; Lim, K; Kim, C. J.; Park, K. B.

2004-01-01

F-18-labeled 2-[ 18 F]fluoro-deoxy-glucose( 18 F-FDG), which is used for PET diagnosis, is generally synthesized by using the nucleophilic substitution method. If 18 O-H 2 O is irradiated by the protons accelerated in a cyclotron, 18F-fluoride is produced by means of nuclear reaction of 18O(p,n)18F. However, 18 O-H 2 O is very expensive and its timely procurement might be difficult because of its frequent world market fluctuations. Therefore, 18 O-H 2 O used for the production of 18 F-FDG should be reused efficiently. When the target 18 O-H 2 O flows the tubes in the synthetic apparatus and ion-exchange resin, it is contaminated by the organic substances such as ethanol, methanol, and acetonitrile, etc. If the recovered target water containing many of these impurities is reused as target water in a cyclotron, abnormal increases of the pressure in the target chamber during irradiation and reduction of the target chamber life-span may occur. As a result, production yield of 18F-fluoride would be decreased, and also the yield of 18 F-FDG. Therefore, organic substances and various metallic ions contained in recovered 18 O-H 2 O must be eliminated prior to its reuse. Moreover, the loss of 18 O-H 2 O during the purification process must be minimized to use the target water economically

Runoff modeling of the Amazon basin using 18 O as a conservative tracer

International Nuclear Information System (INIS)

Mortatti, Jefferson; Victoria, Reynaldo L.; Moraes, Jorge M.; Rodrigues Junior, Jose C.; Matsumoto, Otavio M.

1997-01-01

Using the δO 18 O content of natural waters as a conservative tracer, a runoff modelling of the Amazon river basin was carried out in order to study the hydrological characteristics of the precipitation-runoff relationship. Measurements of the δ 18 O in rainfall waters made in the high Solimoes region at Benjamin Constant, in the central part of basin at Manaus, and at the mouth near the Marajo Island, while the river waters were measured at Obidos only, as a proxy for the mouth, during the 1973-1974 hydrological years. The hydrography separation of the Amazon river was performed using the isotopic method to estimate the contributions of the surface runoff (event water) and baseflow (pre-event water) components to the total river flow. At peak discharge, the average contribution of the baseflow was 57% of the total river flow. The annual average contributions for surface runoff and baseflow were 30.3 and 69.7%, respectively. The residence time of the subsurface water in the basin was estimated as being 7 months, by fitting a sinusoidal function to the isotopic values of rainfall and river waters. The low values of the amplitude damping in the basin suggest high mixing waters during the runoff process. (author). 21 refs., 4 figs., 1 tab

Investigation of the alpha cluster states in 22Ne through the transfer induced breakup reaction 12C (18O, 18O + α)8Be at E(18O) 94.5 MeV

International Nuclear Information System (INIS)

Adhikari, S.; Basu, C.; Mitra, A.K.; Behera, B.R.; Ray, S.; Kumar, Suresh; Chatterjee, A.

2008-01-01

The nucleus 22 Ne like 18 O and 20 Ne has been sparsely investigated experimentally for an 18 O + α cluster structure. Only one experiment has reported the 22 Ne alpha cluster states using the same reaction but a much higher energy. One other experiment also reported the states with a different target and the results of these experiments are different. Therefore the 22 Ne structure has been analyzed in this work

The delta18O composition of Antarctic coastal current waters

International Nuclear Information System (INIS)

Frew, R.; Heywood, K.; Dennis, P.

1997-01-01

The varying proportions of 18 O to 16 O in sea water provide an oceanographic trace like salinity, but with an extra degree of freedom: salt is a tracer for the oceanic fluid, whereas the isotopic composition is a tracer specifically for the water component of that fluid. Hydrogen and oxygen isotopes are the variables most intimately related to the water component in the sea, therefore thay furnish a direct link to the water in the atmosphere and on continents and to the precipitation cycle which caused the salinity changes. The ratio of 18 O to 16 O (delta 18 O) ot waters is a powerful tracer in polar regions where sea and glacial ice processes decouple delta 18 O from salinity. Here we present observations from a significant but relatively unexplored component of the Southern Ocean current system, the Antarctic Coastal Current, and its associated Antarctic Slope Front. (author)

Simplificação do índice CPO dos 18 aos 25 anos DMF Index simplification from 18 to 25 years

Directory of Open Access Journals (Sweden)

Luiz O. C. Guimarães

1990-10-01

Full Text Available O índice CPO pode ser estimado pelo dobro do valor obtido pelo exame de dois hemiarcos (superior direito e inferior esquerdo, e pelo quádruplo do valor observado em seis dentes (primeiro molar e incisivo central superiores direitos, primeiro pré-molar superior esquerdo, segundo molar e incisivo lateral inferiores esquerdos e segundo pré-molar inferior direito. As estimativas foram feitas por métodos da estatística descritiva, em termos de média, composição percentual e coeficiente de prevalência de cárie, tendo-se levantado dados em 100 indivíduos de 18 a 25 anos.The DMF index can be estimated at double the value observed in the exam of two hemiarchs (Upper Right and Lower Left, or at four times the value obtained from six teeth (First Molar and Central Incisor Upper Right, first bicuspid upper left, second molar and lateral incisor lower left and second bicuspid lower right. The estimates were made by the use of methods of descriptive statistics, averages, percentages and the coefficient of the prevalence of caries, in a sample of 100 people, aged from 18 to 25 years.

Letter: Observation of the 16O/18O exchange during electrospray ionization.

Science.gov (United States)

Kostyukevich, Yury; Kononikhin, Alexey; Popov, Igor; Nikolaev, Eugene

2015-01-01

Isotopic exchange approach coupled to high-resolution mass spectrometry has become the power analytical approach for a wide range of analytical and bioanalyticall applications. Considerable efforts have been dedicated to developing fast exchange techniques directly in the ionization source. But all such methods are limited to the hydrogen/deuterium exchange approaches. In this paper we demonstrate that certain types of oxygen atoms can also be exchanged for (18)O on the time scale of the ionization process. Using HIO(3) and NaIO(4) and by infusing the heavy water H(2)(18)O in the ESI source we have demonstrated that it is possible to obtain a high level of oxygen exchange. It was observed that the rate of this exchange depends to a large extent on the temperature of the desolvating capillary of the mass spectrometer. Several other species, such as peptides, oligonucleotides and low weight organic molecules, were subjected to in-ESI (16)O/(18)O exchange but the exchange was not observed.

Inelastic scattering of polarized protons and nuclear deformation in 16O, 18O

International Nuclear Information System (INIS)

de Swiniarski, R.; Pham, D.L.

1984-01-01

Many data concerning inelastic scattering of polarized protons at intermediate energy are now available. We have analyzed some of these data coming from LAMPF at 800 MeV for 16 O (6) and 18 O (7) in order to further study nuclear deformations for these light nuclei. Analyzing powers (A(theta)) and cross-sections ((σ/theta)) for elastic and inelastic scattering of 800 MeV polarized protons from 16 O and 18 O have been analyzed in the coupled-channels (CC) collective model using the code ECIS from Raynal

Co-occurring species differ in tree-ring δ18O trends.

Science.gov (United States)

John D. Marshall; Robert A. Monserud

2006-01-01

The stable oxygen isotope ratio (δ18O) of tree-ring cellulose is jointly determined by the δ18O of xylem water, the δ18O of atmospheric water vapor, the humidity of the atmosphere and perhaps by species-specific differences in leaf structure and function. Atmospheric...

A novel methylation derivatization method for δ(18)O analysis of individual carbohydrates by gas chromatography/pyrolysis-isotope ratio mass spectrometry.

Science.gov (United States)

Lehmann, Marco M; Fischer, Maria; Blees, Jan; Zech, Michael; Siegwolf, Rolf T W; Saurer, Matthias

2016-01-15

The oxygen isotope ratio (δ(18)O) of carbohydrates derived from animals, plants, sediments, and soils provides important information about biochemical and physiological processes, past environmental conditions, and geographical origins, which are otherwise not available. Nowadays, δ(18)O analyses are often performed on carbohydrate bulk material, while compound-specific δ(18)O analyses remain challenging and methods for a wide range of individual carbohydrates are rare. To improve the δ(18)O analysis of individual carbohydrates by gas chromatography/pyrolysis-isotope ratio mass spectrometry (GC/Pyr-IRMS) we developed a new methylation derivatization method. Carbohydrates were fully methylated within 24 h in an easy-to-handle one-pot reaction in acetonitrile, using silver oxide as proton acceptor, methyl iodide as methyl group carrier, and dimethyl sulfide as catalyst. The precision of the method ranged between 0.12 and 1.09‰ for the δ(18)O values of various individual carbohydrates of different classes (mono-, di-, and trisaccharides, alditols), with an accuracy of a similar order of magnitude, despite high variation in peak areas. Based on the δ(18)O values of the main isomers, important monosaccharides such as glucose and fructose could also be precisely analyzed for the first time. We tested the method on standard mixtures, honey samples, and leaf carbohydrates extracted from Pinus sylvestris, showing that the method is also applicable to different carbohydrate mixtures. The new methylation method shows unrivalled accuracy and precision for δ(18)O analysis of various individual carbohydrates; it is fast and easy-to-handle, and may therefore find wide-spread application. Copyright © 2015 John Wiley & Sons, Ltd.

Procedure for rapid determination of δ15N and δ18O values of nitrate: development and application to an irrigated rice paddy watershed.

Science.gov (United States)

Yada, Saeko; Nakajima, Yasuhiro; Itahashi, Sunao; Asada, Kei; Yoshikawa, Seiko; Eguchi, Sadao

2016-01-01

The dual isotope approach using the stable isotope ratios of nitrate nitrogen (δ(15)N(NO3)) and oxygen (δ(18)O(NO3)) is a strong tool for identifying the history of nitrate in various environments. Basically, a rapid procedure for determining δ(15)N(NO3) and δ(18)O(NO3) values is required to analyze many more samples quickly and thus save on the operational costs of isotope-ratio mass spectrometry (IRMS). We developed a new rapid procedure to save time by pre-treating consecutive samples of nitrous oxide microbially converted from nitrate before IRMS determination. By controlling two six-port valves of the pre-treatment system separately, IRMS determination of the current sample and backflush during the next sample pre-treatment period could be conducted simultaneously. A set of 89 samples was analyzed precisely during a 25-h continuous run (17 min per sample), giving the fastest reported processing time, and simultaneously reducing liquid nitrogen and carrier helium gas consumption by 35%. Application of the procedure to an irrigated rice paddy watershed suggested that nitrate concentrations in river waters decreased in a downstream direction, mainly because of the mixing of nitrate from different sources, without distinct evidence of denitrification. Our procedure should help with more detailed studies of nitrate formation processes in watersheds.

Daily δ18O and δD of precipitations from 2007 to 2009 in Guangzhou, South China: Implications for changes of moisture sources

Science.gov (United States)

Xie, Luhua; Wei, Gangjian; Deng, Wenfeng; Zhao, Xiaoli

2011-04-01

SummaryOxygen and hydrogen stable isotopes ( δ18O and δD) in precipitation collected in every event from 2007 to 2009 in Guangzhou, South China, are presented in this paper. The total correlation between δ18O and δD is obtained as δD = (8.46 ± 0.13) δ18O + (15.0 ± 0.9). More negative δ18O and δD generally occur during summer and autumn, while less negative or even positive δ18O and δD occur during winter and spring. Significant negative correlations between precipitation δ18O and temperature, and between precipitation δ18O and precipitation amount are observed. Regression line changes from year to year are likely due to changes in moisture sources for the precipitation. The moisture contributed by adjacent seas or local evaporation account for the main precipitation during winter and early spring, while summer monsoon brings huge amounts of moisture from remote seas associated with higher temperature and larger precipitation amounts. Seasonal variations of the precipitation D-excess provide more details for changes in moisture sources. Higher D-excess values during winter and early spring are estimated to correspond to a lesser proportion of remote moisture, while lower D-excess values during summer and autumn correspond to larger remote moisture transported by summer monsoons. This generally agrees with the results of model analysis on single isobaric backward trajectories for air parcels during specific time periods. Results of this study imply that precipitation δ18O and δD, as well as some related paleoclimate proxies such as δ18O in speleothem and tree ring, and δD in plant-derived organic compounds and tree ring, currently cannot indicate changes in temperature or precipitation amount separately, but should be comprehensive proxies for monsoon climate.

Does δ18O of O2 record meridional shifts in tropical rainfall?

Science.gov (United States)

Seltzer, Alan M.; Buizert, Christo; Baggenstos, Daniel; Brook, Edward J.; Ahn, Jinho; Yang, Ji-Woong; Severinghaus, Jeffrey P.

2017-10-01

Marine sediments, speleothems, paleo-lake elevations, and ice core methane and δ18O of O2 (δ18Oatm) records provide ample evidence for repeated abrupt meridional shifts in tropical rainfall belts throughout the last glacial cycle. To improve understanding of the impact of abrupt events on the global terrestrial biosphere, we present composite records of δ18Oatm and inferred changes in fractionation by the global terrestrial biosphere (ΔɛLAND) from discrete gas measurements in the WAIS Divide (WD) and Siple Dome (SD) Antarctic ice cores. On the common WD timescale, it is evident that maxima in ΔɛLAND are synchronous with or shortly follow small-amplitude WD CH4 peaks that occur within Heinrich stadials 1, 2, 4, and 5 - periods of low atmospheric CH4 concentrations. These local CH4 maxima have been suggested as markers of abrupt climate responses to Heinrich events. Based on our analysis of the modern seasonal cycle of gross primary productivity (GPP)-weighted δ18O of terrestrial precipitation (the source water for atmospheric O2 production), we propose a simple mechanism by which ΔɛLAND tracks the centroid latitude of terrestrial oxygen production. As intense rainfall and oxygen production migrate northward, ΔɛLAND should decrease due to the underlying meridional gradient in rainfall δ18O. A southward shift should increase ΔɛLAND. Monsoon intensity also influences δ18O of precipitation, and although we cannot determine the relative contributions of the two mechanisms, both act in the same direction. Therefore, we suggest that abrupt increases in ΔɛLAND unambiguously imply a southward shift of tropical rainfall. The exact magnitude of this shift, however, remains under-constrained by ΔɛLAND.

Does δ18O of O2 record meridional shifts in tropical rainfall?

Directory of Open Access Journals (Sweden)

A. M. Seltzer

2017-10-01

Full Text Available Marine sediments, speleothems, paleo-lake elevations, and ice core methane and δ18O of O2 (δ18Oatm records provide ample evidence for repeated abrupt meridional shifts in tropical rainfall belts throughout the last glacial cycle. To improve understanding of the impact of abrupt events on the global terrestrial biosphere, we present composite records of δ18Oatm and inferred changes in fractionation by the global terrestrial biosphere (ΔεLAND from discrete gas measurements in the WAIS Divide (WD and Siple Dome (SD Antarctic ice cores. On the common WD timescale, it is evident that maxima in ΔεLAND are synchronous with or shortly follow small-amplitude WD CH4 peaks that occur within Heinrich stadials 1, 2, 4, and 5 – periods of low atmospheric CH4 concentrations. These local CH4 maxima have been suggested as markers of abrupt climate responses to Heinrich events. Based on our analysis of the modern seasonal cycle of gross primary productivity (GPP-weighted δ18O of terrestrial precipitation (the source water for atmospheric O2 production, we propose a simple mechanism by which ΔεLAND tracks the centroid latitude of terrestrial oxygen production. As intense rainfall and oxygen production migrate northward, ΔεLAND should decrease due to the underlying meridional gradient in rainfall δ18O. A southward shift should increase ΔεLAND. Monsoon intensity also influences δ18O of precipitation, and although we cannot determine the relative contributions of the two mechanisms, both act in the same direction. Therefore, we suggest that abrupt increases in ΔεLAND unambiguously imply a southward shift of tropical rainfall. The exact magnitude of this shift, however, remains under-constrained by ΔεLAND.

Late-Holocene hydroclimate and atmospheric circulation variability in southern Patagonia: insights from triple stable isotopes (δ18O, δ13C, δD) of peat bog Sphagnum moss

Science.gov (United States)

Xia, Z.; Yu, Z.; Zheng, Y.; Loisel, J.; Huang, Y.

2017-12-01

The Southern Hemisphere Westerly Winds (SHWWs) exert important influences on regional and global climates, but their long-term behaviors and dynamics are still poorly understood but critical for projecting future changes. Here we present a 5,500-year record from a Sphagnum-dominated peat bog located on the lee side of the Andes at 54.2 °S in southern Patagonia—based on plant macrofossils, Sphagnum cellulose δ18O and δ13C, and lipid δD data—to document and understand the variability in hydroclimate and atmospheric circulation. There is a striking negative correlation between cellulose δ18O and the Southern Annular Mode (SAM) index over the last millennium; particularly the 2.5‰ negative shift of δ18O is concurrent with the observed positive trend in the SAM over the recent decades. The interval of Medieval Climate Anomaly (MCA, 850-600 yr BP) is characterized by a 2.5‰ negative shift of δ18O and low δ13C values, while the Little Ice Age (LIA, 500-300 yr BP) is characterized by a 2.5‰ positive shift of δ18O and high δ13C values. Furthermore, we find the largest negative shift of δ18O ( 3‰) at 2,300 yr BP, suggesting a significantly positive shift in the SAM. We interpret high Sphagnum abundance and high cellulose δ13C values to reflect great moss moisture conditions, while cellulose δ18O variations primarily reflect moisture sources and atmospheric circulation. During the positive phase of SAM (e.g., the MCA and recent decades), strengthened SHWWs enhance the rain-shadow effect, resulting in dry climate and 18O-depleted precipitation (low δ18O values) in the study region. During the negative phase of SAM (e.g., the LIA), weakened SHWWs reduce rain-shadow effect, resulting in wet climate and high δ18O values caused by increases in moisture contributions from the southerly and easterly flows that do not experience strong Rayleigh distillation process during air mass transports. Furthermore, coupling cellulose δ18O and lipid δD enables

{sup 15}N/{sup 14}N isotopic ratio and statistical analysis: an efficient way of linking seized Ecstasy tablets

Energy Technology Data Exchange (ETDEWEB)

Palhol, Fabien; Lamoureux, Catherine; Chabrillat, Martine; Naulet, Norbert

2004-05-10

In this study, the {sup 15}N/{sup 14}N isotopic ratios of 106 samples of 3,4-methylenedioxymethamphetamine (MDMA) extracted from Ecstasy tablets are presented. These ratios, measured using gas chromatography-combustion-isotope ratio mass spectrometry (GC-C-IRMS), show a large discrimination between samples with a range of {delta}{sup 15}N values between -17 and +19%o, depending on the precursors and the method used in clandestine laboratories. Thus, {delta}{sup 15}N values can be used in a statistical analysis carried out in order to link Ecstasy tablets prepared with the same precursors and synthetic pathway. The similarity index obtained after principal component analysis and hierarchical cluster analysis appears to be an efficient way to group tablets seized in different places.

Prognostic value of tumour blood flow, [{sup 18}F]EF5 and [{sup 18}F]FDG PET/CT imaging in patients with head and neck cancer treated with radiochemotherapy

Energy Technology Data Exchange (ETDEWEB)

Komar, Gaber; Eskola, Olli; Sipilae, Hannu; Solin, Olof [Turku PET Centre, Turku (Finland); Lehtioe, Kaisa; Levola, Helena; Lindholm, Paula; Seppaelae, Jan [Turku University Hospital and University of Turku, Department of Oncology and Radiotherapy, Turku (Finland); Seppaenen, Marko [Turku PET Centre, Turku (Finland); Turku University Hospital and University of Turku, Department of Nuclear Medicine, Turku (Finland); Grenman, Reidar [Turku University Hospital and University of Turku, Department of Otorhinolaryngology, Head and Neck Surgery, Turku (Finland); Minn, Heikki [Turku PET Centre, Turku (Finland); Turku University Hospital and University of Turku, Department of Oncology and Radiotherapy, Turku (Finland)

2014-11-15

In order to improve the treatment of squamous cell carcinoma of the head and neck, precise information on the treated tumour's biology is required and the prognostic importance of different biological parameters needs to be determined. The aim of our study was to determine the predictive value of pretreatment PET/CT imaging using [{sup 18}F]FDG, a new hypoxia tracer [{sup 18}F]EF5 and the perfusion tracer [{sup 15}O]H{sub 2}O in patients with squamous cell cancer of the head and neck treated with radiochemotherapy. The study group comprised 22 patients with confirmed squamous cell carcinoma of the head and neck who underwent a PET/CT scan using the above tracers before any treatment. Patients were later treated with a combination of radiochemotherapy and surgery. Parametric blood flow was calculated from dynamic [{sup 15}O]H{sub 2}O PET images using a one-tissue compartment model. [{sup 18}F]FDG images were analysed by calculating standardized uptake values (SUV) and metabolically active tumour volumes (MATV). [{sup 18}F]EF5 images were analysed by calculating tumour-to-muscle uptake ratios (T/M ratio). A T/M ratio of 1.5 was considered a significant threshold and used to determine tumour hypoxic subvolumes (HS) and hypoxic fraction area. The findings were finally correlated with the pretreatment clinical findings (overall stage and TNM stage) as well as the outcome following radiochemotherapy in terms of local control and overall patient survival. Tumour stage and T-classification did not show any significant differences in comparison to the patients' metabolic and functional characteristics measured on PET. Using the Cox proportional hazards model, a shorter overall survival was associated with MATV (p = 0.008, HR = 1.108), maximum [{sup 18}F]EF5 T/M ratio (p = 0.0145, HR = 4.084) and tumour HS (p = 0.0047, HR = 1.112). None of the PET parameters showed a significant effect on patient survival in the log-rank test, although [{sup 18}F]EF5 maximum T

Determination of sup 18 O concentrations in microsamples of biological fluids

Energy Technology Data Exchange (ETDEWEB)

Cohen, D D [Australian Nuclear Science and Technology Organisation (ANSTO), Menai (Australia); Bradshaw, S D; Bradshaw, F J [University of Western Australia, Perth (Australia). Dept. of Zoology; Katsaros, A [Australian Inst. of Nuclear Science and Engineering (AINSE), Menai (Australia)

1990-04-01

The {sup 18}O(p, {alpha}){sup 15}N reaction has been developed for the analysis of microsamples of biological fluids containing {sup 18}O-enriched water. Samples as small as 50 {mu}l have been used. Well characterized Ta{sub 2}O{sub 5} targets were prepared from these fluids and irradiated with several hundred nA of protons from the 3 MV Van de Graaff at Lucas Heights. The broad (47 keV) 846 kV resonance in this reaction was used to measure {sup 18}O concentrations down to natural backgrounds (0.2 at.%) in a few minutes of accelerator running time. Concentrations of {sup 18}O from 0 to 5 at.% were measured in body fluids in small Australian lizards directly after doping with {sup 18}O-enriched water and then again after several days of roaming around in their natural desert environments. The changes in these levels were related to the metabolic rates of these animals. (orig.).

Influence of different organic fertilizers on quality parameters and the delta(15)N, delta(13)C, delta(2)H, delta(34)S, and delta(18)O values of orange fruit (Citrus sinensis L. Osbeck).

Science.gov (United States)

Rapisarda, Paolo; Camin, Federica; Fabroni, Simona; Perini, Matteo; Torrisi, Biagio; Intrigliolo, Francesco

2010-03-24

To investigate the influence of different types of fertilizers on quality parameters, N-containing compounds, and the delta(15)N, delta(13)C, delta(2)H, delta (34)S, and delta(18)O values of citrus fruit, a study was performed on the orange fruit cv. 'Valencia late' (Citrus sinensis L. Osbeck), which was harvested in four plots (three organic and one conventional) located on the same farm. The results demonstrated that different types of organic fertilizers containing the same amount of nitrogen did not effect important changes in orange fruit quality parameters. The levels of total N and N-containing compounds such as synephrine in fruit juice were not statistically different among the different treatments. The delta(15)N values of orange fruit grown under fertilizer derived from animal origin as well as from vegetable compost were statistically higher than those grown with mineral fertilizer. Therefore, delta(15)N values can be used as an indicator of citrus fertilization management (organic or conventional), because even when applied organic fertilizers are of different origins, the natural abundance of (15)N in organic citrus fruit remains higher than in conventional ones. These treatments also did not effect differences in the delta(13)C, delta(2)H, delta(34)S, and delta(18)O values of fruit.

Development of O-18 stable isotope separation technology using membrane

Energy Technology Data Exchange (ETDEWEB)

Kim, Jae Woo; Kim, Taek Soo; Choi, Hwa Rim; Park, Sung Hee; Lee, Ki Tae; Chang, Dae Shik

2006-06-15

The ultimate goal of this investigation is to develop the separation technology for O-18 oxygen stable isotope used in a cyclotron as a target for production of radioisotope F-18. F-18 is a base material for synthesis of [F-18]FDG radio-pharmaceutical, which is one of the most important tumor diagnostic agent used in PET (Positron Emission Tomography). More specifically, this investigation is focused on three categories as follow, 1) development of the membrane distillation isotope separation process to re-enrich O-18 stable isotope whose isotopic concentration is reduced after used in a cyclotron, 2) development of organic impurity purification technology to remove acetone, methanol, ethanol, and acetonitrile contained in a used cyclotron O-18 enriched target water, and 3) development of a laser absorption spectroscopic system for analyzing oxygen isotopic concentration in water.

The effect of carbonic anhydrase on the kinetics and equilibrium of the oxygen isotope exchange in the CO2-H2O system: Implications for δ18O vital effects in biogenic carbonates

Science.gov (United States)

Uchikawa, Joji; Zeebe, Richard E.

2012-10-01

Interpretations of the primary paleoceanographic information recorded in stable oxygen isotope values (δ18O) of biogenic CaCO3 can be obscured by disequilibrium effects. CaCO3 is often depleted in 18O relative to the δ18O values expected for precipitation in thermodynamic equilibrium with ambient seawater as a result of vital effects. Vital effects in δ18O have been explained in terms of the influence of fluid pH on the overall δ18O of the sum of dissolved inorganic carbon (DIC) species (often referred to as "pH model") and in terms of 18O depletion as a result of the kinetic effects associated with CO2 hydration (CO2 + H2O ↔ H2CO3 ↔ HCO3- + H+) and CO2 hydroxylation (CO2 + OH- ↔ HCO3-) in the calcification sites (so-called "kinetic model"). This study addresses the potential role of an enzyme, carbonic anhydrase (CA), that catalyzes inter-conversion of CO2 and HCO3- in relation to the underlying mechanism of vital effects. We performed quantitative inorganic carbonate precipitation experiments in order to examine the changes in 18O equilibration rate as a function of CA concentration. Experiments were performed at pH 8.3 and 8.9. These pH values are comparable to the average surface ocean pH and elevated pH levels observed in the calcification sites of some coral and foraminiferal species, respectively. The rate of uncatalyzed 18O exchange in the CO2-H2O system is governed by the pH-dependent DIC speciation and the kinetic rate constant for CO2 hydration and hydroxylation, which can be summarized by a simple mathematical expression. The results from control experiments (no CA addition) are in agreement with this expression. The results from control experiments also suggest that the most recently published kinetic rate constant for CO2 hydroxylation has been overestimated. When CA is present, the 18O equilibration process is greatly enhanced at both pH levels due to the catalysis of CO2 hydration by the enzyme. For example, the time required for 18O

Destruction of /sup 18/O in red giants. A search for a sub-threshold resonance in the /sup 18/O+p system

Energy Technology Data Exchange (ETDEWEB)

Champagne, A E; Pitt, M L

1986-09-08

The /sup 18/O(/sup 3/He,d)/sup 19/F reaction has been used to determine if a presumed sub-threshold resonance at Esub(c.m.)=-94 KeV in the /sup 18/O(p,..cap alpha..)/sup 15/N reaction exists at an astrophysically significant level. No evidence for this state was observed which implies a dimensionless reduced width thetasub(p)/sup 2/<5 . 10/sup -5/. In addition, a proton width GAMMAsub(p)=2 x 10/sup -19/ eV has been determined for a d-wave resonance located at Esub(c.m.)=20 keV. The resulting thermonuclear reaction rate is slow enough to ensure that /sup 18/O is not destroyed at red-giant temperatures.

The δ2H and δ18O of tap water from 349 sites in the United States and selected territories

Science.gov (United States)

Coplen, Tyler B.; Landwehr, Jurate M.; Qi, Haiping; Lorenz, Jennifer M.

2013-01-01

Because the stable isotopic compositions of hydrogen (δ2H) and oxygen (δ18O) of animal (including human) tissues, such as hair, nail, and urine, reflect the δ2H and δ18O of water and food ingested by an animal or a human and because the δ2H and δ18O of environmental waters vary geographically, δ2H and δ18O values of tap water samples collected in 2007-2008 from 349 sites in the United States and three selected U.S. territories have been measured in support of forensic science applications, creating one of the largest databases of tap water δ2H and δ18O values to date. The results of replicate isotopic measurements for these tap water samples confirm that the expanded uncertainties (U = 2μc) obtained over a period of years by the Reston Stable Isotope Laboratory from δ2H and δ18O dual-inlet mass spectrometric measurements are conservative, at ±2‰ and ±0.2 ‰, respectively. These uncertainties are important because U.S. Geological Survey data may be needed for forensic science applications, including providing evidence in court cases. Half way through the investigation, an isotope-laser spectrometer was acquired, enabling comparison of dual-inlet isotope-ratio mass spectrometric results with isotope-laser spectrometric results. The uncertainty of the laser-based δ2H measurement results for these tap water samples is comparable to the uncertainty of the mass spectrometric method, with the laser-based method having a slightly lower uncertainty. However, the δ18O uncertainty of the laser-based method is more than a factor of ten higher than that of the dual-inlet isotoperatio mass spectrometric method.

Reconstruction of water mass properties of the Western Mediterranean using stable isotope ratios (δ18O and δ13C) from Pinna nobilis shells

Science.gov (United States)

Garcia-March, Jose Rafael; Surge, Donna; Tena-Medialdea, Jose; Torres, Javi; Garcia-Martinez, Micaela

2017-04-01

We analysed the stable isotope ratios (δ18O and δ13C) from the calcite of the outer prismatic layer of 8 Pinna nobilis shells at a rate of c. 12-16 samples/year for years between 1997 and 2013. These produced 8 time series between 4 and 16 years long. The empty shells had been collected in two Spanish marine protected areas, Tabarca Island in Alicante and Columbretes Islands in Castellón (4 specimens each). For all shells we constrained the time of death within at least a halve year window. The present study completes previous calibrations by using recorded seawater temperature data during at least two years for each site, coinciding with part of the analysed periods in the shells. Our preliminary results clearly reflect the seasonality of the signal in δ18O values for the entire ontogeny of the individuals studied. However, one specimen from Tabarca Island sampled between years 4 and 11 (corresponding to real age) shows a clear ontogenetic change, with an abrupt reduction in the amplitude of the signal from age 6 to 11 for both δ18O and δ13C values. We hypothesize this pattern relates to the onset of first gonad maturation. Values of δ13C track δ18O values in most individuals, but 3 specimens show low amplitude. For all time series, δ13C values show a decreasing slope with ontogeny similar to previous observations in P. nobilis and other bivalves. Estimated seawater temperature from our δ18O time series reveals the potential of P. nobilis shells as valuable archives of Mediterranean temperature reconstructions in the context of climate change.

The effect of acid rain and altitude on concentration, δ34S, and δ18O of sulfate in the water from Sudety Mountains, Poland

Science.gov (United States)

Szynkiewicz, Anna; Modelska, Magdalena; Jedrysek, Mariusz Orion; Mastalerz, Maria

2008-01-01

The analyses of sulfate content, δ34S and δ18O of dissolved sulfate, and δ18O of water were carried out in a 14 km2 crystalline massif located in the Sudety Mountains (SW Poland) to 1) assess the amount of the sulfate delivered to the surface and groundwater systems by modern atmospheric precipitation, 2) determine the effect of altitude on these parameters, and 3) investigate their seasonal variations. In April and November of 2002, August 2003, and March and September of 2005, samples of water were collected from springs and streams of the massif. During these seasons, sulfate contents and δ18O(SO42−) values varied from 5.80 to 18.00 mg/l and from 3.96 to 8.23‰, respectively, showing distinctively higher values ofδ18O(SO42−) in wet seasons. The δ34S(SO42−) values had a relatively narrow range from 4.09 to 5.28‰ and were similar to those reported for organic matter in soil and the canopy throughfall in the Sudety Mountains.

The Oxygen Isotopic Composition (18O/16O) in the Dust of Comet 67P/Churyumov-Gerasimenko Measured by COSIMA On-board Rosetta

Science.gov (United States)

Paquette, J. A.; Engrand, C.; Hilchenbach, M.; Fray, N.; Stenzel, O. J.; Silen, J.; Rynö, J.; Kissel, J.

2018-03-01

The oxygen isotopic ratio 18O/16O has been measured in cometary gas for a wide variety of comets, but the only measurements in cometary dust were performed by the Stardust cometary sample return mission. Most such measurements find a value of the ratio that is consistent with Vienna Standard Mean Ocean Water (VSMOW) within errors. In this work we present the result of a measurement, using the COSIMA instrument on the Rosetta orbiter, of the oxygen isotopic ratio in dust from Comet 67P/Churyumov-Gerasimenko. Measuring the 18O/16O ratio with COSIMA is challenging for a number of reasons, but it is possible with a reasonable degree of precision. We find a result of 2.00 × 10-3 ± 1.2 × 10-4 which is consistent within errors with VSMOW.

Separating Long-Lived Metal Ions from {sup 18}F During H{sub 2} {sup 18}O Recovery

Energy Technology Data Exchange (ETDEWEB)

Schueller, Michael John; Alexoff, David L.; Schlyer, David James [Medical Department, Brookhaven National Laboratory, 57 Cornell Street, Upton NY 11973 (United States)

2009-07-01

Cyclotron targets for the production of [{sup 18}F]fluoride usually use a thin metal window to contain the {sup 18}O enriched water during irradiation. This window is activated by the proton beam, and undesired radioisotopes can enter the target water. A pre-packaged strong anion exchange resin is commonly used for [{sup 18}O]-water recovery. A two-column method has been developed which delivers >95% of the [18F]fluoride for radiosynthesis while rejecting >99.9% of the contaminants. (author)

Search for the two-photon decay of the 2+ first excited states in 18O and 28Si

International Nuclear Information System (INIS)

Music, M.

1986-01-01

The present work describes an attempt to measure the probability for the two-photon transition between two adjacent nuclear states in the presence of an allowed, strongly predominant one-photon decay, using the Heidelberg-Darmstadt Crystal Ball Spectrometer. The branching ratios of the two-photon decay of the first excited, 2 + levels of 18 O and 28 Si relative to the one-photon, E2 transitions to the 0 + ground states were determined to be: Wγγ/Wγ = (0.7±2.4) x 10 -6 for the 2 + >0 + transition in 18 O and Wγγ/Wγ = (1.6±1.8) x 10 -6 for the 2 + >0 + transition in 28 Si. Since both results are consistent with zero, it is possible to express them as the upper limits for the two-photon decay (3 δ) of 7.9 x 10 -6 of 18 O and 6.9 x 10 -6 of 28 Si 2 + levels. These values are by far the smallest ones reported to be observed in a two-photon decay of a nuclear state. For 18 O, the result disproves theoretical estimates of the corresponding two-photon E1F1 matrix element was well as experimental values deduced from multiple-Coulomb-excitation measurements. The main experimental difficulties were caused by the gamma rays from one-photon transitions and were found to be connected with cross-talk events due to Bremsstrahlung of Compton electrons and not - as generally believed - positron annihilation in flight. (orig.)

Elastic and inelastic scattering of 18O ions on 12C nuclei

Directory of Open Access Journals (Sweden)

A. T. Rudchik

2009-12-01

Full Text Available Angular distributions of the 12C + 18O elastic and inelastic scattering were measured at the energy Elab(18O = 105 MeV (Ec.m. = 42 MeV. These data and data known from the literature at the energies Ec.m. = 12.9 - 56 МеV were analysed within the optical model and coupled-reactionchannels method. The sets of the Woods-Saxon (12С + 18O-potential parameters were deduced and their energy dependence was studied. It was found the isotopic differences in the (12С + 16O- and (12С + 18O-potentials parameters and in their surface forms. The mechanisms of elastic and inelastic (12С + 18O-scattering and role of transfer reactions were studied.

A 50-year record of NOx and SO{sub 2} sources in precipitation in the Northern Rocky Mountains, USA - article no. 4

Energy Technology Data Exchange (ETDEWEB)

Naftz, D.L.; Schuster, P.F.; Johnson, C.A. [US Geological Survey, Salt Lake City, UT (United States)

2011-03-07

Ice-core samples from Upper Fremont Glacier (UFG), Wyoming, were used as proxy records for the chemical composition of atmospheric deposition. Results of analysis of the ice-core samples for stable isotopes of nitrogen ({delta}{sup 15}, NO{sub 3}{sup -}) and sulfur ({delta}{sup 34}S, SO{sub 4}{sup 2}), as well as NO{sub 3}{sup -} and SO{sub 4}{sup 2} deposition rates from the late-1940s through the early-1990s, were used to enhance and extend existing National Atmospheric Deposition Program/National Trends Network (NADP/NTN) data in western Wyoming. The most enriched {delta}{sup 34}S value in the UFG ice-core samples coincided with snow deposited during the 1980 eruption of Mt. St. Helens, Washington. The remaining {delta}{sup 34}S values were similar to the isotopic composition of coal from southern Wyoming. The {delta}{sup 15}N values in ice-core samples representing a similar period of snow deposition were negative, ranging from -5.9 to -3.2 parts per thousand and all fall within the {delta}{sup 15}N values expected from vehicle emissions. Ice-core nitrate and sulfate deposition data reflect the sharply increasing U.S. emissions data from 1950 to the mid-1970s.

Oxygen isotope effect in YBa2Cu3O7 prepared by burning YBa2Cu3 in 16O and 18O

Science.gov (United States)

Yvon, Pascal J.; Schwarz, R. B.; Pierce, C. B.; Bernardez, L.; Conners, A.; Meisenheimer, R.

1989-04-01

We prepared YBa2Cu3 powder by ball milling a 2:1 molar mixture of the intermetallics BaCu and CuY. We synthesized YBa2Cu3(16O)7-x and YBa2Cu3(18O)7-x by oxidizing the YBa2Cu3 powder in 16O and 18O. The 16O/18O ratios were determined by laser-ionization and sputtering-ionization mass spectroscopy. The YBa2Cu3(160)7-x sample had 99.8 at. %16O, and the YBa2Cu3(18O)7-x sample had 96.5 at. %18O. Susceptibility measurements of the superconducting transition temperature (Tc=91.7 K for 16O; half-point transition at 84 K show an isotope effect of 0.4+/-0.1 K.

Study of groundwater in the Chicu River basin, Sabana de Bogota, Colombia; Estudio de las aguas subterraneas de la cuenca del Rio Chicu, Sabana de Bogota, Colombia

Energy Technology Data Exchange (ETDEWEB)

Obando G, E; Jimenez B, G; Torres Q, E; Alayon C, E; Garavito B, F [Instituto de Ciencias Nucleares y Energias Alternativas, INEA, Bogota (Colombia)

1995-10-01

The Rio Chicu Valley aquifer system represents one of the many sub-systems constituting the hydrogeological system of the Sabana de Bogota. The valley has a structure of a graben, covered by a quaternary alluvial formation, which has a low permeability and therefore is an aquifer of poor characteristics. Due to the thickness of this aquifer (around 300 m), the tertiary aquifers are only exploited by few deep wells. The isotopic composition of water collected from the tertiary aquifer is depleted by 1 per mille in {delta}{sup 18}O and 8 per mille in {delta}D. This difference is due to the altitude effect of recharge, because the tertiary aquifers outcrop on the top of the surrounding hills. In some places, the stable isotope content of water sampled in wells tapping water from the quaternary aquifer is similar to the values found in the tertiary aquifer. This fact indicates the ascending leakage from deep horizons. A rather unique characteristics of the quaternary aquifer is that in the central part of the basin the dissolved inorganic carbon DIC is very high and shows a {delta}{sup 13}C values around +10 per mille vs PDB and {sup 14}C around 5-10 pmc. The positive values are probably related to decomposition of organic matter in anaerobic conditions. These values reflect a very low flow in the system and limited recharge. (author). 1 ref., 5 figs, 2 tabs.

Improved online δ18O measurements of nitrogen- and sulfur-bearing organic materials and a proposed analytical protocol

Science.gov (United States)

Qi, H.; Coplen, T.B.; Wassenaar, L.I.

2011-01-01

It is well known that N2 in the ion source of a mass spectrometer interferes with the CO background during the δ18O measurement of carbon monoxide. A similar problem arises with the high-temperature conversion (HTC) analysis of nitrogenous O-bearing samples (e.g. nitrates and keratins) to CO for δ18O measurement, where the sample introduces a significant N2 peak before the CO peak, making determination of accurate oxygen isotope ratios difficult. Although using a gas chromatography (GC) column longer than that commonly provided by manufacturers (0.6 m) can improve the efficiency of separation of CO and N2 and using a valve to divert nitrogen and prevent it from entering the ion source of a mass spectrometer improved measurement results, biased δ18O values could still be obtained. A careful evaluation of the performance of the GC separation column was carried out. With optimal GC columns, the δ18O reproducibility of human hair keratins and other keratin materials was better than ±0.15 ‰ (n = 5; for the internal analytical reproducibility), and better than ±0.10 ‰ (n = 4; for the external analytical reproducibility).

Prognostic value of 18F-FLT PET in patients with neuroendocrine neoplasms

DEFF Research Database (Denmark)

Johnbeck, Camilla B.; Knigge, Ulrich; Langer, Seppo W.

2016-01-01

Neuroendocrine neoplasms (NENs) constitute a heterogeneous group of tumors arising in various organs and with a large span of aggressiveness and survival rates. The Ki-67 proliferation index is presently used as the key marker of prognosis, and treatment guidelines are largely based on this index...... study was to investigate 18F-FLT PET as a prognostic marker for NENs in comparison with 18F-FDG PET and Ki-67 index. Methods: One hundred patients were PET-scanned with both 18F-FLT and 18F-FDG within the same week, and the prognostic value of a positive scan was examined in terms of progression...... prognostic value in NEN patients but when 18F-FDG PET and Ki-67 index are also available, a multivariate model revealed that 18F-FLT PET only adds information regarding PFS but not OS, whereas 18F-FDG PET remains predictive of both PFS and OS. However, a clinically robust algorithm including 18F...

USGS48 Puerto Rico precipitation - A new isotopic reference material for δ2H and δ18O measurements of water

Science.gov (United States)

Qi, Haiping; Coplen, Tyler B.; Tarbox, Lauren V.; Lorenz, Jennifer M.; Scholl, Martha A.

2014-01-01

A new secondary isotopic reference material has been prepared from Puerto Rico precipitation, which was filtered, homogenised, loaded into glass ampoules, sealed with a torch, autoclaved to eliminate biological activity, and calibrated by dual-inlet isotope-ratio mass spectrometry. This isotopic reference material, designated as USGS48, is intended to be one of two isotopic reference waters for daily normalisation of stable hydrogen (δ2H) and stable oxygen (δ18O) isotopic analysis of water with a mass spectrometer or a laser absorption spectrometer. The δ2H and δ18O values of this reference water are−2.0±0.4 and−2.224±0.012 ‰, respectively, relative to Vienna Standard Mean Ocean Water on scales normalised such that the δ2H and δ18O values of Standard Light Antarctic Precipitation reference water are−428 and−55.5 ‰, respectively. Each uncertainty is an estimated expanded uncertainty (U=2uc) about the reference value that provides an interval that has about a 95 % probability of encompassing the true value. This isotopic reference water is available by the case of 144 glass ampoules containing 5 mL of water in each ampoule.

LIMS for Lasers 2015 for achieving long-term accuracy and precision of δ2H, δ17O, and δ18O of waters using laser absorption spectrometry

Science.gov (United States)

Coplen, Tyler B.; Wassenaar, Leonard I

2015-01-01

RationaleAlthough laser absorption spectrometry (LAS) instrumentation is easy to use, its incorporation into laboratory operations is not easy, owing to extensive offline manipulation of comma-separated-values files for outlier detection, between-sample memory correction, nonlinearity (δ-variation with water amount) correction, drift correction, normalization to VSMOW-SLAP scales, and difficulty in performing long-term QA/QC audits.MethodsA Microsoft Access relational-database application, LIMS (Laboratory Information Management System) for Lasers 2015, was developed. It automates LAS data corrections and manages clients, projects, samples, instrument-sample lists, and triple-isotope (δ17O, δ18O, and δ2H values) instrumental data for liquid-water samples. It enables users to (1) graphically evaluate sample injections for variable water yields and high isotope-delta variance; (2) correct for between-sample carryover, instrumental drift, and δ nonlinearity; and (3) normalize final results to VSMOW-SLAP scales.ResultsCost-free LIMS for Lasers 2015 enables users to obtain improved δ17O, δ18O, and δ2H values with liquid-water LAS instruments, even those with under-performing syringes. For example, LAS δ2HVSMOW measurements of USGS50 Lake Kyoga (Uganda) water using an under-performing syringe having ±10 % variation in water concentration gave +31.7 ± 1.6 ‰ (2-σ standard deviation), compared with the reference value of +32.8 ± 0.4 ‰, after correction for variation in δ value with water concentration, between-sample memory, and normalization to the VSMOW-SLAP scale.ConclusionsLIMS for Lasers 2015 enables users to create systematic, well-founded instrument templates, import δ2H, δ17O, and δ18O results, evaluate performance with automatic graphical plots, correct for δ nonlinearity due to variable water concentration, correct for between-sample memory, adjust for drift, perform VSMOW-SLAP normalization, and perform long-term QA/QC audits

Analysis of stable isotope ratios (δ18O and δ2H) in precipitation of the Verde River watershed, Arizona 2003 through 2014

Science.gov (United States)

Beisner, Kimberly R.; Paretti, Nicholas V.; Tucci, Rachel S.

2016-04-25

Stable isotope delta values (δ18O and δ2H) of precipitation can vary with elevation, and quantification of the precipitation elevation gradient can be used to predict recharge elevation within a watershed. Precipitation samples were analyzed for stable isotope delta values between 2003 and 2014 from the Verde River watershed of north-central Arizona. Results indicate a significant decrease in summer isotopic values overtime at 3,100-, 4,100-, 6,100-, 7,100-, and 8,100-feet elevation. The updated local meteoric water line for the area is δ2H = 7.11 δ18O + 3.40. Equations to predict stable isotopic values based on elevation were updated from previous publications in Blasch and others (2006), Blasch and Bryson (2007), and Bryson and others (2007). New equations were separated for samples from the Camp Verde to Flagstaff transect and the Prescott to Chino Valley transect. For the Camp Verde to Flagstaff transect, the new equations for winter precipitation are δ18O = -0.0004z − 8.87 and δ2H = -0.0029z − 59.8 (where z represents elevation in feet) and the summer precipitation equations were not statistically significant. For the Prescott to Chino Valley transect, the new equations for summer precipitation are δ18O = -0.0005z − 3.22 and δ2H = -0.0022z − 27.9; the winter precipitation equations were not statistically significant and, notably, stable isotope values were similar across all elevations. Interpretation of elevation of recharge contributing to surface and groundwaters in the Verde River watershed using the updated equations for the Camp Verde to Flagstaff transect will give lower elevation values compared with interpretations presented in the previous studies. For waters in the Prescott and Chino Valley area, more information is needed to understand local controls on stable isotope values related to elevation.

A robotic system for 18F-FMISO PET-guided intratumoral pO2 measurements.

Science.gov (United States)

Chang, Jenghwa; Wen, Bixiu; Kazanzides, Peter; Zanzonico, Pat; Finn, Ronald D; Fichtinger, Gabor; Ling, C Clifton

2009-11-01

An image-guided robotic system was used to measure the oxygen tension (pO2) in rodent tumor xenografts using interstitial probes guided by tumor hypoxia PET images. Rats with approximately 1 cm diameter tumors were anesthetized and immobilized in a custom-fabricated whole-body mold. Imaging was performed using a dedicated small-animal PET scanner (R4 or Focus 120 microPET) approximately 2 h after the injection of the hypoxia tracer 18F-fluoromisonidazole (18F-FMISO). The coordinate systems of the robot and PET were registered based on fiducial markers in the rodent bed visible on the PET images. Guided by the 3D microPET image set, measurements were performed at various locations in the tumor and compared to the corresponding 18F-FMISO image intensity at the respective measurement points. Experiments were performed on four tumor-bearing rats with 4 (86), 3 (80), 7 (162), and 8 (235) measurement tracks (points) for each experiment. The 18F-FMISO image intensities were inversely correlated with the measured pO2, with a Pearson coefficient ranging from -0.14 to -0.97 for the 22 measurement tracks. The cumulative scatterplots of pO2 versus image intensity yielded a hyperbolic relationship, with correlation coefficients of 0.52, 0.48, 0.64, and 0.73, respectively, for the four tumors. In conclusion, PET image-guided pO2 measurement is feasible with this robot system and, more generally, this system will permit point-by-point comparison of physiological probe measurements and image voxel values as a means of validating molecularly targeted radiotracers. Although the overall data fitting suggested that 18F-FMISO may be an effective hypoxia marker, the use of static 18F-FMISO PET postinjection scans to guide radiotherapy might be problematic due to the observed high variation in some individual data pairs from the fitted curve, indicating potential temporal fluctuation of oxygen tension in individual voxels or possible suboptimal imaging time postadministration of hypoxia

Form factors and transition charge density of 16O and 18O nuclei

International Nuclear Information System (INIS)

Gul'karov, I.S.; Vakil', R.Kh.

1986-01-01

A formula is obtained for the transition density of charge (TDC) in the Helm model. The form factors are analysed for inelastic scattering of electrons On the 16 O isotopes (O 1 + , 6.052 MeV; 2 1 + , 6.917 MeV) and on the 18 O isotopes (0 1 + , 3.630 MeV; 2 1 + , 1.982 MeV; 0 2 + , 3.919 MeV; 2 3 + , 5.250 MeV; 4 1 + , 3.553 MeV; 4 2 + , 7.114 MeV). For monopole transitions the TDC is of the volume kind, but for L=2 and 4 transitions the TDC has a maximum at approximately R (R is the nuclear surface radius). There are as well obtained the first TDC moments, i.e. the reduced transition probabilities and transition radii of 16 O and 18 O

Excitation of the lowest 1- state in 18O by scattering from 16O

International Nuclear Information System (INIS)

Carter, J.; Sellschop, J.P.F.; Clarkson, R.G.; Hnizdo, V.; Osterfeld, F.; Frahn, W.E.; Richter, A.

1981-01-01

The 1 - (4.45 MeV) state in 18 O, together with the 2 + (1.98 MeV) and 3 - (5.09 MeV) states, were excited by inelastic scattering from 16 O at E(lab)=35 MeV. In an attempt to understand the 1 - excitation, various macroscopic models, including a ralationship derived recently by Frahn, were considered. However, this excitation was found to be best explained by a microscopic description. A comparison is made with inelastic α-scattering from 18 O [af

Calcium manganese oxides as oxygen evolution catalysts: O2 formation pathways indicated by 18O-labelling studies.

Science.gov (United States)

Shevela, Dmitriy; Koroidov, Sergey; Najafpour, M Mahdi; Messinger, Johannes; Kurz, Philipp

2011-05-02

Oxygen evolution catalysed by calcium manganese and manganese-only oxides was studied in (18)O-enriched water. Using membrane-inlet mass spectrometry, we monitored the formation of the different O(2) isotopologues (16)O(2), (16)O(18)O and (18)O(2) in such reactions simultaneously with good time resolution. From the analysis of the data, we conclude that entirely different pathways of dioxygen formation catalysis exist for reactions involving hydrogen peroxide (H(2)O(2)), hydrogen persulfate (HSO(5)(-)) or single-electron oxidants such as Ce(IV) and [Ru(III) (bipy)(3)](3+) . Like the studied oxide catalysts, the active sites of manganese catalase and the oxygen-evolving complex (OEC) of photosystem II (PSII) consist of μ-oxido manganese or μ-oxido calcium manganese sites. The studied processes show very similar (18)O-labelling behaviour to the natural enzymes and are therefore interesting model systems for in vivo oxygen formation by manganese metalloenzymes such as PSII. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Comparison of one and two-neutron transfer near the Coulomb barrier for the 27Al(18O, 16O)29Al, 27Al(18O, 17O)28Al and 27Al(13C, 12C)28Al reactions

International Nuclear Information System (INIS)

Schiller, S.A.; Eck, J.S.

1975-01-01

Total reaction cross sections for the transfer reactions 27 Al( 18 O, 16 O) 29 Al, 27 Al( 18 O, 17 O) 28 Al and 27 Al( 13 C, 12 C) 28 Al are reported for center-of-mass energies between 13 and 20 MeV for 18 O projectiles and between 11 and 17.5 MeV for 13 C projectiles. The reaction products, 29 Al, and 28 Al, beta decay to 29 Si and 28 Si, respectively, and the subsequent γ decays of 29 Si and 28 Si were measured. Due to the relatively long beta decay half lives, data were taken in a beam-off mode, resulting in very clean spectra. Total cross sections were calculated and compared with a theoretical model for barrier penetration proposed by C.Y. Wong. Differences between 18 O induced one and two-neutron total transfer reaction cross sections are discussed. (orig.) [de

A new derivatization method for δ18O analysis of individual carbohydrates with GC-Pyrolysis-IRMS

Science.gov (United States)

Lehmann, M. M.; Siegwolf, R. T.; Saurer, M.; Blees, J.; Fischer, M.; Zech, M.

2015-12-01

Compound specific isotope analysis (CSIA) with gas chromatography coupled to an isotope ratio mass spectrometer (GC-Pyr-IRMS) is nowadays a powerful tool that is widely used by a broad spectrum of research fields to investigate the isotopic signature of diverse metabolites. While many CSIA methods for carbon, hydrogen, and nitrogen isotopes are known, CSIA methods for the analysis of oxygen isotopes (δ18O) are still not widely established. Especially, reliable and precise methods for the δ18O analyses of individual carbohydrates are scarce, which is caused by the highly sensitive nature of the sugars. However, carbohydrates are important components of living organisms, source for many biochemical reactions, and can be found in all organisms, in soils, sediments, and in air. Thus, a method, allowing the investigation of the 18O/16O ratio in carbohydrates will enhance the scope of research using isotopes. We developed a new and easy to handle derivatization method to determine δ18O in carbohydrates with GC-Pyr-IRMS that consists of a catalyzed one-pot reaction in acetonitrile, resulting in complete methylation of all sugar hydroxyl groups within 24 hours, with silver oxide as the proton acceptor and methyl iodide as the methyl group carrier. Results derived from standard material show unrivalled δ18O precision ranging from about 0.2 to 1.1 ‰ for different individual carbohydrates of different classes and a generally very good accuracy, with a narrow range of 0.2 ‰ around the reference value, despite of high area variations. We applied this method on real samples, demonstrating that the method can commonly be used for analyzing honey samples, and for the analyses of more complex carbohydrate mixtures from plant leaves, including glucose, fructose, pinitol, and sucrose. Our new method may be used for food, beverage, and medical applications, as well as for biogeochemical and paleoclimatic sciences.

Determination of the δ15N and δ18O of nitrate in water; RSIL lab code 2900

Science.gov (United States)

Coplen, Tyler B.; Qi, Haiping; Revesz, Kinga; Casciotti, Karen; Hannon, Janet E.

2007-01-01

The purpose of the Reston Stable Isotope Laboratory (RSIL) lab code 2900 is to determine the δ15N and δ18O of nitrate (NO3-) in water. The δ15N and δ18O of the dissolved NO3- are analyzed by converting the NO3- to nitrous oxide (N2O), which serves as the analyte for mass spectrometry. A culture of denitrifying bacteria is used in the enzymatic conversion of the NO3- to N2O, which follows the pathway shown in equation 1: NO3- → NO2- → NO → 1/2 N2O (1) Because the bacteria Pseudomonas aureofaciens lack N2O reductive activity, the reaction stops at N2O, unlike the typical denitrification reaction that goes to N2. After several hours, the conversion is complete, and the N2O is extracted from the vial, separated from volatile organic vapor and water vapor by an automated -65 °C isopropanol-slush trap, a Nafion drier, a CO2 and water removal unit (Costech #021020 carbon dioxide absorbent with Mg(ClO4)2), and trapped in a small-volume trap immersed in liquid nitrogen with a modified Finnigan MAT (now Thermo Scientific) GasBench 2 introduction system. After the N2O is released, it is further purified by gas chromatography before introduction to the isotope-ratio mass spectrometer (IRMS). The IRMS is a Thermo Scientific Delta V Plus continuous flow IRMS (CF-IRMS). It has a universal triple collector, consisting of two wide cups with a narrow cup in the middle; it is capable of simultaneously measuring mass/charge (m/z) of the N2O molecule 44, 45, and 46. The ion beams from these m/z values are as follows: m/z = 44 = N2O = 14N14N16O; m/z = 45 = N2O = 14N15N16O or 14N14N17O; m/z = 46 = N2O = 14N14N18O. The 17O contributions to the m/z 44 and m/z 45 ion beams are accounted for before δ15N values are reported.

δ18O of apatite phosphate in small pelagic fish: insights from wild-caught and tank-grown specimens

Science.gov (United States)

Lambert, T.; Javor, B.; Paytan, A.

2011-12-01

Oxygen isotope ratios of mineralized structures in fish reflect the temperature and isotopic composition of the water in which they grow. For bulk samples (e.g., whole scales, bones, and otoliths), understanding how this signal is integrated across time and space is critical, especially for organisms exposed to high variability in growth conditions. Here, we assess the response of fish scale δ18O (from apatite phosphate) to experimentally manipulated water conditions. Wild-caught sardines were grown at controlled temperatures (13°C, 17°C, and 21°C) for 11 months. Higher growth temperatures correlated to lower δ18O values, representing a combination of scale apatite deposited before and after the temperature manipulation. Models that account for both biomineral allometry and exposure to varying water properties (e.g., by overlaying migration routes, isoscapes, and temperature maps) have the potential to quantify the varying contributions of minerals grown under different conditions. We use this method to predict δ18O of apatite phosphate for small pelagic fish found in California coastal waters, then compare expected values to those obtained from collected samples. Since phosphate oxygen is relatively resistant to diagenesis, this modern calibration establishes a framework for paleo studies.

The co-evolution of seawater δ18O and δD

Science.gov (United States)

Pope, E. C.

2017-12-01

The δ18O of marine carbonate and silica precipitates has increased by 15‰ over the last ca. 3.5 billion years. Whether this shift reflects a parallel increase in oxygen isotope compositions of seawater with time, Precambrian atmospheric temperatures >55°C, or complete alteration of ancient samples during diagenesis, remains controversial despite nearly a half-century of debate. Early mass balance models of the modern ocean system suggested near constant δ18OSEAWATER over time due to the buffering capacity of fresh oceanic crust. However, fluxes controlling 18O sources and sinks to the ocean (high-temperature alteration of the seafloor, and low-temperature weathering of continental and ocean crust, respectively) have not remained fixed throughout Earth history. I adapted published mass balance models for δ18OSEAWATER to evaluate how continental growth, the subaerial emergence of continents, and decreasing mantle temperature affect the magnitude of 18O sources and sinks, and thus the evolution of seawater δ18O since the early Archean. These factors also affect the δD of seawater, which is controlled by the flux of water between mantle, crustal and glacial reservoirs, such that its evolution can be used as an independent constraint on the magnitude that these variables have had on δ18O evolution. The models indicate that a key parameter controlling δ18OSEAWATER is the flux of water between the mantle and free water of the exosphere. Recent geophysical models suggest that the capacity for subducting slabs to sequester water into the deep ocean has increased as the mantle has cooled. Hydrous minerals in subducted oceanic crust have a net δ18O lower than seawater. Incomplete recycling of water from these phases in subduction zones results in progressive removal of 16O from the ocean and thus can explain a significant portion of the increase in δ18O recorded in the marine sediment record. However, mass balance constraints on the global hydrogen budget limits

The quadrupole moment of the first excited state of 18O

International Nuclear Information System (INIS)

Fewel, M.P.; Baxter, A.M.; Kean, D.C.; Spear, R.H.

1976-11-01

Using the re-orientation effect in Coulomb excitation, the quadrupole moment, Qsub(2 + ), of the first excited state of 18 O is found to be -0.100 +- 0.030 eb. The analysis assumes, on the basis of previous measurements, that B(E2; 0 + → 2 + ) = 0.0044 +- 0.0004 e 2 b 2 . A correction (+0.032 eb) for the effect of the giant dipole resonance, based on the hydrodynamic model, has been applied. Evidence is presented that some other determinations of Qsub(2 + ) were performed at too high a bombarding energy. The present value of Qsub(2 + ) is smaller in magnitude than that reported by Kleinfeld et al. (1975), but remains larger than the value of -0.034 eb predicted by a recent shell-model calculation. (Author)

36 CFR 18.5 - May property be leased without receiving fair market value rent?

Science.gov (United States)

2010-07-01

... without receiving fair market value rent? 18.5 Section 18.5 Parks, Forests, and Public Property NATIONAL... leased without receiving fair market value rent? Property may be leased under this part only if the lease requires payment of rent to the government equal to or higher than the property's fair market value rent...

Geochronology and Fluid-Rock Interaction Associated with the Nopal I Uranium Deposit, Pena Blanca, Mexico

Energy Technology Data Exchange (ETDEWEB)

M. Fayek; P. Goodell; M. Ren; A. Simmons

2005-07-11

The Nopal I uranium (U) deposit, Pena Blanca District, Mexico, largely consists of secondary U{sup 6+} minerals, which occur within a breccia pipe mainly hosted by the 44 Ma Nopal and Colorados volcanic formations. These two units overly the Pozos conglomerate formation and Cretaceous limestone. Three new vertical diamond drill holes (DDHs) were recently drilled at Nopal I. DDH-PB1 with continuous core was drilled through the Nopal I deposit and two additional DDHs were drilled {approx}50 m on either side of the cored hole. These DDHs terminate 20 m below the current water table, thus allowing the detection of possible gradients in radionuclide contents resulting from transport from the overlying uranium deposit. Primary uraninite within the main ore body is rare and fine-grained ({approx}50 micrometers), thus making geochronology of the Nopal I deposit very difficult. Uranium, lead and oxygen isotopes can be used to study fluid-uraninite interaction, provided that the analyses are obtained on the micro-scale. Secondary ionization mass spectrometry (SIMS) permits in situ measurement of isotopic ratios with a spatial resolution on the scale of a few {micro}m. Preliminary U-Pb results show that uraninite from the main ore body gives an age of 32 {+-} 8 Ma, whereas uraninite from the uraniferous Pozos conglomerate that lies nearly 100 m below the main ore body and 25 meters above the water table, gives a U-Pb age that is <1 Ma. Oxygen isotopic analyses show that uraninite from the ore body has a {delta}{sup 18}O = -10.8{per_thousand}, whereas the uraninite within the Pozos conglomerate has a {delta}{sup 18}O = +1.5{per_thousand}. If it is assumed that both uraninites precipitated from meteoric water ({delta}{sup 18}O = -7{per_thousand}), then calculated precipitation temperatures are 55 C for the uraninite from the ore body and 20 C for uraninite hosted by the Pozos conglomerate. These temperatures are consistent with previous studies that calculated precipitation

Evaluation of the use of activated carbon for the filtration of gaseous effluents generated in the production of the radiopharmaceutical FDG-{sup 18}F; Avaliação do uso de carvão ativado para filtração de efluentes gasosos gerados na produção do radiofármaco FDG-{sup 18}F

Energy Technology Data Exchange (ETDEWEB)

Cunha, R.S.; Goulart, A.S.; Flores, M.R.; Saibt, M., E-mail: rafael@nucleorad.com.br [NUCLEORAD Soluções em Proteção Radiológica, Porto Alegre, RS (Brazil)

2017-07-01

Gaseous rejects generated in the production of FDG-{sup 18}F are produced mainly during the irradiation of the enriched water (H2O{sup 18}) within the niobium / target body at the cyclotron accelerator and during the process of FDG-{sup 18}F synthesis in the synthesizer modules within the cell hot. In order to reduce the levels of gaseous effluents emitted, activated carbon filters are used in the exhaust system. These have the ability to adsorb the {sup 18}F gaseous molecules generated in the synthesis. This work aims to quantify the efficiency of the activated carbon filters in relation to the dose rate before and after the passage of the gases through the filtration system. To quantify the values in the exhaust system, two radiation detectors were used, in the equivalent dose rate mode in μSv/h. To evaluate the values obtained, graphs of the levels before and after the filtration system were generated. These graphs were compared to each other, relating the values found. The generated graphs showed a high efficiency in the filtration of gaseous effluents. Several dose rate peaks are presented in the exhaust system during FDG-{sup 18}F synthesis, however after the passage of the gases through the filters these peaks become values very close to the Background values.

Reconstruction of drip-water δ18O based on calcite oxygen and clumped isotopes of speleothems from Bunker Cave (Germany

Directory of Open Access Journals (Sweden)

T. Kluge

2013-02-01

Full Text Available The geochemical signature of many speleothems used for reconstruction of past continental climates is affected by kinetic isotope fractionation. This limits quantitative paleoclimate reconstruction and, in cases where the kinetic fractionation varies with time, also affects relative paleoclimate interpretations. In carbonate archive research, clumped isotope thermometry is typically used as proxy for absolute temperatures. In the case of speleothems, however, clumped isotopes provide a sensitive indicator for disequilibrium effects. The extent of kinetic fractionation co-varies in Δ47 and δ18O so that it can be used to account for disequilibrium in δ18O and to extract the past drip-water composition. Here we apply this approach to stalagmites from Bunker Cave (Germany and calculate drip-water δ18Ow values for the Eemian, MIS3, and the Holocene, relying on independent temperature estimates and accounting for disequilibrium. Applying the co-variation method to modern calcite precipitates yields drip-water δ18Ow values in agreement with modern cave drip-water δ18Ow of −7.9 ± 0.3‰, despite large and variable disequilibrium effects in both calcite δ18Oc and Δ47. Reconstructed paleo-drip-water δ18Ow values are lower during colder periods (e.g., MIS3: −8.6 ± 0.4‰ and the early Holocene at 11 ka: −9.7 ± 0.2‰ and show higher values during warmer climatic periods (e.g., the Eemian: −7.6 ± 0.2‰ and the Holocene Climatic Optimum: −7.2 ± 0.3‰. This new approach offers a unique possibility for quantitative climate reconstruction including the assessment of past hydrological conditions while accounting for disequilibrium effects.

Secondary biological coalbed gas in the Xinji area, Anhui province, China: Evidence from the geochemical features and secondary changes

Energy Technology Data Exchange (ETDEWEB)

Tao, Mingxin [Key Laboratory of Environmental Change and Natural Disaster of Ministry of Education, College of Resources Sciences and Technology, Beijing Normal University, Beijing 100875 (China); Key Laboratory of Gas Geochemistry, Institute of Geology and Geophysics, Chinese Academy of Sciences, Lanzhou 730000 (China); Shi, Baoguang; Wang, Wanchun; Li, Xiaobin; Gao, Bo [Key Laboratory of Gas Geochemistry, Institute of Geology and Geophysics, Chinese Academy of Sciences, Lanzhou 730000 (China); Li, Jinying [Material and Environment College, Qindao University of Science and Technology, Qindao 266042 (China)

2007-07-02

In order to ascertain the origin of the coalbed gas in the Xinji area, Anhui Province of China, the paper examined the geochemical features and secondary changes of CH{sub 4}, C{sub 2}H{sub 6}, CO{sub 2} and N{sub 2} from the coalbed gas. The related gas composition, carbon isotope and tracer geochemical data are as follows: 0.993 to 1.0 for C{sub 1}/C{sub 1-n}, 188.6 to 2993.7 for C{sub 1}/C{sub 2}, < 2% for CO{sub 2}, 0.64 to 3.06% for [CO{sub 2}/(CO{sub 2} + CH{sub 4})]100%, - 50.7 permille to - 61.3 permille for {delta}{sup 13}C{sub 1} with the average value of - 56.6 permille, - 15.9 permille to - 26.7 permille for {delta}{sup 13}C{sub 2}, - 10.8 permille to - 25.3 permille for {delta}{sup 13}C{sub 3}, - 6.0 permille to - 39.0 permille for {delta}{sup 13}C{sub CO2} with the average value of - 17.9 permille, 30.7 permille to 43.9 permille for {delta}{delta}{sup 13}C{sub C2-C1}, and 17.2 permille to 50 permille for {delta}{delta}{sup 13}C{sub CO2-C1}, - 1 permille to + 1 permille for {delta}{sup 15}N{sub N2}, 1.13 x 10{sup -7} to 3.20 x 10{sup -7} for {sup 3}He/{sup 4}He with R/Ra ratios range from 0.08 to 0.23. The Ro values of the coal range from 0.88% to 0.91%. The trends of the {delta}{sup 13}C{sub 1} values and {delta}{sup 13}C{sub CO2} values downward in the stratigraphic profile are opposite: the former appears as a slight light-heavy-light trend, but the latter appears as a heavy-light-heavy trend. The {delta}{sup 13}C{sub 1} values have a negative correlation with the {delta}{sup 13}C{sub CO2} values. However, the {delta}{sup 13}C{sub 2} values have no correlation with the {delta}{sup 13}C{sub 1} values due to its complicated variation. The thermal evolution of the coal in the Xinji area is in the phase of a lot of wet gas generation, but most of the CO{sub 2} and heavy hydrocarbons have been reduced or degraded by microbes and have changed into biogenic methane. The coalbed gas is comprised of secondary biogenic methane, thermogenic methane, the

The systematics of the (18O,20Ne) reaction and its application to the determination of the mass excess of 122Cd

International Nuclear Information System (INIS)

Kruechten, B. van.

1987-01-01

The aim of the thesis should be the determination of the mass excess of the neutron-deficient nucleus 122 Cd with the ( 18 O, 20 Ne) reaction proved for light target nuclei (A lab ≤ 15 0 ) lay below the detection limit of 1 μb/sr it was first necessary to determine optimum kinematical conditions for the study of the reaction 124 Sn( 18 O, 20 Ne). For this purpose systematic studies of the angular distributions of the ( 18 O, 20 Ne) reaction on target nuclei with mass numbers between 28 ( 28 Si) and 208 ( 208 Pb) were performed at beam energies of 82, 102, 141, and 189 MeV. The evaluation of these measurements gave first information on the dependences of the cross sections on energy, Q-value, target mass, and angle. For the 124 Sn( 18 O, 20 Ne) 122 Cd reaction a maximum cross section of about 1 μb/sr at a beam energy 30 MeV above the Coulomb threshold (100 MeV) and a laboratory angle of 40 0 could be expected. In a new experiment this prediction could be verified. The analysis of the measured spectra yielded a Q-value for the 124 Sn( 18 O, 20 Ne) 122 Cd reaction of 0.1 ± 0.44 MeV. The mass excess of -82.08 ± 0.44 MeV calculated from this for 122 Cd is by 1.5 MeV more positive than the prediction of the Wapstra table. (orig./HSI) [de

Oxygen 18 concentration profile measurements near the surface by 18O(p,α)15N resonance reaction

International Nuclear Information System (INIS)

Amsel, G.; David, D.

1975-01-01

The method of spectrum reduction in nuclear reaction microanalysis does not allow to obtain depth resolutions better than the order of 2000A. Resolutions of the order of 200A may be obtained by using the narrow resonance technique, when applied to thin films. The latter technique was extended to thick targets, with deep concentration profiles presenting a sharp gradient near the surface. This method is presented and illustrated by the study of 18 O profiles in oxygen diffusion measurements in growing ZrO 2 , using the 629keV resonance of the reaction 18 O(p,α) 15 N [fr

Building materials as intrinsic sources of sulphate: A hidden face of salt weathering of historical monuments investigated through multi-isotope tracing (B, O, S)

Energy Technology Data Exchange (ETDEWEB)

Kloppmann, W., E-mail: w.kloppmann@brgm.fr [BRGM, BP 6009, F-45060 Orleans cedex 2 (France); Bromblet, P.; Vallet, J.M. [CICRP, 21, rue Guibal, F-13003 Marseille (France); Verges-Belmin, V. [LRMH, 29, rue de Paris, F-77420 Champs sur Marne (France); Rolland, O. [Independent restorer, 3, rue du Gue, 37270 Montlouis s/Loire (France); Guerrot, C. [BRGM, BP 6009, F-45060 Orleans cedex 2 (France); Gosselin, C. [BRGM, BP 6009, F-45060 Orleans cedex 2 (France); LRMH, 29, rue de Paris, F-77420 Champs sur Marne (France)

2011-04-01

Sulphate neoformation is a major factor of degradation of stone monuments. Boron, sulphur and oxygen isotope signatures were investigated for five French historical monuments (Bourges, Chartres and Marseille cathedrals, Chenonceau castle, and Versailles garden statues) to investigate the role of intrinsic sulphate sources (gypsum plasters and mortars) in stone degradation, compared to the influence of extrinsic sources such as atmospheric pollution. Gypsum plasters and gypsum-containing mortars fall systematically in the {delta}{sup 34}S and {delta}{sup 18}O range of Paris Basin Eocene evaporites indicating the origin of the raw materials (so-called 'Paris plaster'). Black crusts show the typical S and O isotope signatures observed elsewhere in Europe that can be attributed to atmospheric pollution, together with a marine component for Marseille. Boron isotopes for black crusts indicate coal combustion as principal boron source. Mortar isotope compositions discriminate three types, one similar to gypsum plasters, one strongly depleted in {sup 34}S, attributed to pyrite oxidation, and a third one close to atmospheric sulphates. The isotopic composition of sulphates and boron of most degraded building stones of the different monuments is well explained by the identified sulphate sources. In several cases (in particular for Chenonceau and Bourges, to some extent for Chartres), the impact of gypsum plaster as building and restoration material on the degradation of the stones in its vicinity was clearly demonstrated. The study illustrates the usefulness of multi-isotope studies to investigate stone degradation factors, as the combination of several isotope systematics increases the discriminatory power of isotope studies with respect to contaminant sources. - Research Highlights: {yields} Insight in stone weathering mechanisms by multi-isotope fingerprinting (B, S, O). {yields} Intrinsic sulphate sources (gypsum plaster, mortar) contribute to stone degradation

18O and 34S in the Upper Bartonium gypsum deposits of the Paris basin

International Nuclear Information System (INIS)

Fontes, J.C.; Letolle, R.

1976-01-01

Isotopic analyses ( 18 O and 34 S) of the Eocene gypsum from the Paris basin show a range beyond the normal Tertiary marine values. The possibility of a reduction process during diagenesis is discussed. A hypothesis of continental origin by leaching of Permotriassic deposits is proposed for this formation on the basis of a comparison of the isotopic contents recorded from Germany and eastern France

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

Spatial Isotopic Characterization of Slovak Groundwaters

Energy Technology Data Exchange (ETDEWEB)

Povinec, P. P.; Sivo, A.; Breier, R.; Richtarikova, M. [Comenius University, Faculty of Mathematics, Physics and Informatics, Bratislava (Slovakia); Zenisova, Z. [Comenius University, Faculty of Natural Sciences, Bratislava (Slovakia); Aggarwal, P. K.; Araguas Araguas, L. [International Atomic Energy Agency, Isotope Hydrology Section, Vienna (Austria)

2013-07-15

Zitny ostrov (Rye Island) in the south west of Slovakia is the largest groundwater reservoir in Central Europe (about 10 Gm{sup 3}). Groundwater contamination with radionuclides, heavy metals and organic compounds from the Danube River and local industrial and agricultural activities has recently been of great concern. Geostatistical analysis of experimental isotope data has been carried out with the aim of better understanding groundwater dynamics. For this purpose, spatial variations in the distribution of water isotopes and radiocarbon in the groundwater of Zitny ostrov have been evaluated. Subsurface water profiles showed enriched {delta}{sup 18}O levels at around 20 m water depth, and depleted values below 30 m, which are similar to those observed in the Danube River. The core of the subsurface {sup 14}C profiles represents contemporary groundwater with {sup 14}C values above 80 pMc. (author)

Direct Synthesis of ESBO Derivatives-18O Labelled with Dioxirane

Directory of Open Access Journals (Sweden)

Stefano La Tegola

2013-01-01

Full Text Available This work addresses a new approach developed in our laboratory, consisting in the application of isolated dimethyldioxirane (DDO, 1a labelled with 18O for synthesis of epoxidized glyceryl linoleate (Gly-LLL, 2. We expect that this work could contribute in improving analytical methods for the determination of epoxidized soybean oil (ESBO in complex food matrices by adopting an 18O-labelled-epoxidized triacylglycerol as an internal standard.

Direct Synthesis of ESBO Derivatives-18O Labelled with Dioxirane

OpenAIRE

La Tegola, Stefano; Annese, Cosimo; Suman, Michele; Tommasi, Immacolata; Fusco, Caterina; D'Accolti, Lucia

2013-01-01

This work addresses a new approach developed in our laboratory, consisting in the application of isolated dimethyldioxirane (DDO, 1a) labelled with 18O for synthesis of epoxidized glyceryl linoleate (Gly-LLL, 2). We expect that this work could contribute in improving analytical methods for the determination of epoxidized soybean oil (ESBO) in complex food matrices by adopting an 18O-labelled-epoxidized triacylglycerol as an internal standard.

Fourier Transform Spectroscopy of 18O-Enriched Carbonyl Sulfide from 1825 to 2700 cm -1

Science.gov (United States)

Strugariu, T.; Naı̈m, S.; Fayt, A.; Bredohl, H.; Blavier, J.-F.; Dubois, I.

1998-06-01

We have measured the Fourier transform spectrum of carbonyl sulfide from 1825 to 2700 cm-1, using a sample enriched in both18O (94.0%) and17O (1.54%). A careful calibration yields a line-position accuracy between 1.5 and 3.0 10-5cm-1. We have observed and analyzed 118 infrared bands of which 93 are measured for the first time: 55 for18O12C32S, 20 for18O12C34S, 11 for18O12C33S, 1 for18O12C36S, 12 for17O12C32S, 4 for17O12C34S, 2 for17O12C33S, and 13 for18O13C32S. Intensities are also reported and analyzed for all those bands. The intensity accuracy is better than 10%, and the precision of approximately 1% allows us to determine some Herman-Wallis coefficients.

Similar speleothem δ18O signals indicating diverging climate variations in inland central Asia and monsoonal south Asia during the Holocene

Science.gov (United States)

Jin, Liya; Zhang, Xiaojian

2017-04-01

High-resolution and precisely dated speleothem oxygen isotope (δ18O) records from Asia have provided key evidence for past monsoonal changes. It is found that δ18O records of stalagmites from Kesang Cave (42°52'N, 81°45'E, Xinjiang, China) in inland central Asia were very similar to those from Qunf Cave (17°10'N, 54°18'E, southern Oman) in South Asia, shifting from light to heavy throughout the Holocene, which was regarded as a signal that strong Asian summer monsoon (ASM) may have intruded into the Kesang Cave site and/or adjacent areas in inland central Asia to produce heavy rainfall during the high insolation times (e.g. the early Holocene). However, this is in contrast to conclusions based on other Holocene proxy records and modeling simulations, showing a persistent wetting trend in arid central Asia during the Holocene with a dryer condition in the early Holocene and the wettest condition in the late Holocene. With an analysis of model-proxy data comparison, we revealed a possible physical mechanism responsible for the Holocene evolution of moisture/precipitation in Asian summer monsoon (ASM)-dominated regions and that in the inland central Asia. It is revealed that a recurrent circumglobal teleconnection (CGT) pattern in the summertime mid-latitude circulation of the Northern Hemisphere was closely related to the ASM and the climate of inland central Asia, acting as a bridge linking the ASM to insolation, high-latitude forcing (North Atlantic sea surface temperature (SST)), and low-latitude forcing (tropical Ocean SST). Also, the CGT influence speleothem δ18O values in South Asia via its effect on the amount of precipitation. In addition, the moisture source from the Indian Ocean is associated with relatively high δ18O values compared with that from the North Atlantic Ocean, leading to increased precipitation δ18O values. Hence, the CGT has probably been the key factor responsible for the in-phase relationship in speleothem δ18O values (Kesang Cave

Annual Growth Bands in Hymenaea courbaril

Energy Technology Data Exchange (ETDEWEB)

Westbrook, J A; Guilderson, T P; Colinvaux, P A

2004-02-09

One significant source of annual temperature and precipitation data arises from the regular annual secondary growth rings of trees. Several tropical tree species are observed to form regular growth bands that may or may not form annually. Such growth was observed in one stem disk of the tropical legume Hymenaea courbaril near the area of David, Panama. In comparison to annual reference {Delta}{sup 14}C values from wood and air, the {Delta}{sup 14}C values from the secondary growth rings formed by H. courbaril were determined to be annual in nature in this one stem disk specimen. During this study, H. courbaril was also observed to translocate recently produced photosynthate into older growth rings as sapwood is converted to heartwood. This process alters the overall {Delta}{sup 14}C values of these transitional growth rings as cellulose with a higher {Delta}{sup 14}C content is translocated into growth rings with a relatively lower {Delta}{sup 14}C content. Once the annual nature of these growth rings is established, further stable isotope analyses on H. courbaril material in other studies may help to complete gaps in the understanding of short and of long term global climate patterns.

Calibration of δ13C and δ18O measurements in CO2 using Off-axis Integrated Cavity Output Spectrometer (ICOS)

Science.gov (United States)

Joseph, Jobin; Külls, Christoph

2014-05-01

The δ13C and δ18O of CO2 has enormous potential as tracers to study and quantify the interaction between the water and carbon cycles. Isotope ratio mass spectrometry (IRMS) being the conventional method for stable isotopic measurements, has many limitations making it impossible for deploying them in remote areas for online or in-situ sampling. New laser based absorption spectroscopy approaches like Cavity Ring Down Spectroscopy (CRDS) and Integrated Cavity Output Spectroscopy (ICOS) have been developed for online measurements of stable isotopes at an expense of considerably less power requirement but with precision comparable to IRMS. In this research project, we introduce a new calibration system for an Off- Axis ICOS (Los Gatos Research CCIA-36d) for a wide range of varying concentrations of CO2 (800ppm - 25,000ppm), a typical CO2 flux range at the plant-soil continuum. The calibration compensates for the concentration dependency of δ13C and δ18O measurements, and was performed using various CO2 standards with known CO2 concentration and δC13 and δO18 values. A mathematical model was developed after the calibration procedure as a correction factor for the concentration dependency of δ13C and δ18O measurements. Temperature dependency of δ13C and δ18O measurements were investigated and no significant influence was found. Simultaneous calibration of δ13C and δ18O is achieved using this calibration system with an overall accuracy of (~ 0.75±0.24 ‰ for δ13C, ~ 0.81 ±0.26‰ for δ18O). This calibration procedure is found to be appropriate for making Off-Axis ICOS suitable for measuring CO2 concentration and δ13C and δ18O measurements at atmosphere-plant-soil continuum.

Determination of the δ15N and δ18O of nitrate in solids; RSIL lab code 2897

Science.gov (United States)

Coplen, Tyler B.; Qi, Haiping; Revesz, Kinga; Casciotti, Karen; Hannon, Janet E.

2007-01-01

The purpose of the Reston Stable Isotope Laboratory (RSIL) lab code 2897 is to determine the δ15N and δ18O of nitrate (NO3-) in solids. The NO3- fraction of the nitrogen species is dissolved by water (called leaching) and can be analyzed by the bacterial method covered in RSIL lab code 2900. After leaching, the δ15N and δ18O of the dissolved NO3- is analyzed by conversion of the NO3- to nitrous oxide (N2O), which serves as the analyte for mass spectrometry. A culture of denitrifying bacteria is used in the enzymatic conversion of NO3- to N2O, which follows the pathway shown in equation 1: NO3- → NO2- → NO → 1/2 N2O (1) Because the bacteria Pseudomonas aureofaciens lack N2O reductive activity, the reaction stops at N2O, unlike the typical denitrification reaction that goes to N2. After several hours, the conversion is complete, and the N2O is extracted from the vial, separated from volatile organic vapor and water vapor by an automated -65 °C isopropanol-slush trap, a Nafion drier, a CO2 and water removal unit (Costech #021020 carbon dioxide absorbent with Mg(ClO4)2), and trapped in a small-volume trap immersed in liquid nitrogen with a modified Finnigan MAT (now Thermo Scientific) GasBench 2 introduction system. After the N2O is released, it is further purified by gas chromatography before introduction to the isotope-ratio mass spectrometer (IRMS). The IRMS is a Thermo Scientific Delta V Plus continuous flow IRMS (CF-IRMS). It has a universal triple collector, consisting of two wide cups with a narrow cup in the middle; it is capable of simultaneously measuring mass/charge (m/z) of the N2O molecule 44, 45, and 46. The ion beams from these m/z values are as follows: m/z = 44 = N2O = 14N14N16O; m/z = 45 = N2O = 14N15N16O or 14N14N17O; m/z = 46 = N2O = 14N14N18O. The 17O contributions to the m/z 44 and m/z 45 ion beams are accounted for before δ15N values are reported.

Avaliação do cumprimento da NR-18 em função do porte de obra residencial e proposta de lista de verificação da NR-18

Directory of Open Access Journals (Sweden)

Marcelo Fabiano Costella

Full Text Available O presente trabalho investiga as reais condições dos ambientes de trabalho da indústria da construção, tendo em vista os problemas relacionados à segurança do trabalho nos canteiros de obras. Formulou-se a hipótese de haver discrepância no grau de cumprimento da NR-18 em obras de diferentes portes (pequena, média e grande. Baseado em uma lista de verificação do grau de cumprimento dos requisitos da NR-18, foram avaliados 115 canteiros de obra na cidade de Chapecó - SC. Para cada item da lista de verificação foi atribuída uma nota e, após compilar as informações, estas foram avaliadas conforme os objetivos da pesquisa. Fez-se uma análise crítica para os cinco piores e os cinco melhores itens observados para as obras pequenas, médias e grandes. Analisando-se os resultados é possível afirmar que há uma diferença significativa de aplicação da NR-18 nos diferentes portes de obras, sendo que as obras de grande porte obtiveram uma média final (6,47 significativamente superior em relação às obras pequenas (1,97. Desta forma, foi corroborada a hipótese formulada, podendo se atribuir este resultado a diversos fatores, entre os quais a falta de habilidades gerenciais de segurança e saúde do trabalho nas pequenas empresas. Outra contribuição deste artigo foi a proposta de uma nova lista de verificação para avaliar o grau de cumprimento da NR-18 nos canteiros de obra.

Simulation and optimization of stable isotope 18O separation by water vacuum distillation

International Nuclear Information System (INIS)

Chen Yuyan; Qin Chuanjiang; Xiao Bin; Xu Jing'an

2012-01-01

In the research, a stable isotope 18 O separation column was set up by water vacuum distillation with 20 m packing height and 0.1 m diameter of the column. The self-developed special packing named PAC- 18 O was packed inside the column. Firstly, a model was created by using the Aspen Plus software, and then the simulation results were validated by test results. Secondly, a group of simulation results were created by Aspen Plus, and the optimal operation conditions were gotten by using the artificial neural network (ANN) and Statistica software. Considering comprehensive factors drawn from column pressure and from withdrawing velocity, conclusions were reached on the study of the impact on the abundance of the isotope 18 O. The final results show that the abundance of the isotope 18 O increases as column pressure dropping and withdrawing velocity decreasing. Besides, the optimal column pressure and the incidence formula between the abundance of the isotope 18 O and withdrawing velocity were gotten. The conclusion is that the method of simulation and optimization can be applied to 18 O industrial design and will be popular in traditional distillation process to realize optimization design. (authors)

Reconstructing lake evaporation history and the isotopic composition of precipitation by a coupled δ18O-δ2H biomarker approach

Science.gov (United States)

Hepp, Johannes; Tuthorn, Mario; Zech, Roland; Mügler, Ines; Schlütz, Frank; Zech, Wolfgang; Zech, Michael

2015-10-01

Over the past decades, δ18O and δ2H analyses of lacustrine sediments became an invaluable tool in paleohydrology and paleolimnology for reconstructing the isotopic composition of past lake water and precipitation. However, based on δ18O or δ2H records alone, it can be challenging to distinguish between changes of the precipitation signal and changes caused by evaporation. Here we propose a coupled δ18O-δ2H biomarker approach that provides the possibility to disentangle between these two factors. The isotopic composition of long chain n-alkanes (n-C25, n-C27, n-C29, n-C31) were analyzed in order to establish a 16 ka Late Glacial and Holocene δ2H record for the sediment archive of Lake Panch Pokhari in High Himalaya, Nepal. The δ2Hn-alkane record generally corroborates a previously established δ18Osugar record reporting on high values characterizing the deglaciation and the Older and the Younger Dryas, and low values characterizing the Bølling and the Allerød periods. Since the investigated n-alkane and sugar biomarkers are considered to be primarily of aquatic origin, they were used to reconstruct the isotopic composition of lake water. The reconstructed deuterium excess of lake water ranges from +57‰ to -85‰ and is shown to serve as proxy for the evaporation history of Lake Panch Pokhari. Lake desiccation during the deglaciation, the Older Dryas and the Younger Dryas is affirmed by a multi-proxy approach using the Hydrogen Index (HI) and the carbon to nitrogen ratio (C/N) as additional proxies for lake sediment organic matter mineralization. Furthermore, the coupled δ18O and δ2H approach allows disentangling the lake water isotopic enrichment from variations of the isotopic composition of precipitation. The reconstructed 16 ka δ18Oprecipitation record of Lake Panch Pokhari is well in agreement with the δ18O records of Chinese speleothems and presumably reflects the Indian Summer Monsoon variability.

Assessing the fidelity of marine vertebrate microfossil δ18O signatures and their potential for palaeo-ecological and -climatic reconstructions

Energy Technology Data Exchange (ETDEWEB)

Roelofs, Brett; Barham, Milo; Cliff, John; Joachimski, Michael; Martin, Laure; Trinajstic, Kate

2017-01-01

Conodont biogenic apatite has become a preferred analytical target for oxygen isotope studies investigating ocean temperature and palaeoclimate change in the Palaeozoic. Despite the growing application in geochemical based palaeoenvironmental reconstructions, the paucity or absence of conodont fossils in certain facies necessitates greater flexibility in selection of robust oxygen bearing compounds for analysis. Microvertebrates offer a potential substitute for conodonts from the middle Palaeozoic. Microvertebrate bioapatite is particularly advantageous given a fossil record extending to the present with representatives across freshwater to fully marine environments, thus widening the scope of oxygen isotope studies on bioapatite. However, significant tissue heterogeneity within vertebrates and differential susceptibility of these tissues to diagenetic alteration have been raised as potential problems affecting the reliability of the oxygen isotope ratios as palaeoclimate proxies. Pristine microvertebrate and co-occurring conodont fossils from the Late Devonian and Early Carboniferous of the Lennard Shelf, Canning Basin, Western Australia, were analysed using bulk (gas isotope ratio mass spectrometry) and in-situ (secondary ion mass spectrometry) methodologies, with the latter technique allowing investigation of specific tissues within vertebrate elements. The δ18Oconodont results may be interpreted in terms of palaeolatitudinally and environmentally sensible palaeotemperatures and provide a baseline standard for comparison against δ18Omicrovertebrate values. Despite an absence of obvious diagenetic influences, GIRMS of microvertebrate denticles yielded δ18O values depleted by 2-4 ‰ relative to co-occurring conodonts. SIMS analysis of hypermineralised tissues in both scales and teeth produced δ18O values comparable with those of associated conodonts. The susceptibility of porous phosphatic fossil tissues to microbial activity, fluid interaction and

Using delta15N- and delta18O-values to identify nitrate sources in karst ground water, Guiyang, southwest China.

Science.gov (United States)

Liu, Cong-Qiang; Li, Si-Liang; Lang, Yun-Chao; Xiao, Hua-Yun

2006-11-15

Nitrate pollution of the karstic groundwater is an increasingly serious problem with the development of Guiyang, the capital city of Guizhou Province, southwest China. The higher content of NO3- in groundwater compared to surface water during both summer and winter seasons indicates that the karstic groundwater system cannot easily recover once contaminated with nitrate. In order to assess the sources and conversion of nitrate in the groundwater of Guiyang, we analyzed the major ions, delta(15)N-NH4+, delta(15)N-NO3-, and delta(18)O-NO3- in surface and groundwater samples collected during both summer and winter seasons. The results show that nitrate is the major dominant species of nitrogen in most water samples and there is a big variation of nitrate sources in groundwater between winter and summer season, due to fast response of groundwater to rain or surface water in the karst area. Combined with information on NO3- /Cl-, the variations of the isotope values of nitrate in the groundwater show a mixing process of multiple sources of nitrate, especially in the summer season. Chemical fertilizer and nitrification of nitrogen-containing organic materials contribute nitrate to suburban groundwater, while the sewage effluents and denitrification mainly control the nitrate distribution in urban groundwater.

Isotopic and Geochemical Signatures of Melgaco CO{sub 2} Rich Cold Mineralwaters, NW Portugal

Energy Technology Data Exchange (ETDEWEB)

Carreira, P. M.; Nunes, D. [Instituto Tecnologico e Nuclear, Unidade de Ciencias Quimicas e Radiofarmaceuticas, Sacavem (Portugal); Marques, J. M. [Instituto Superior Tecnico, Universidade Tecnica de Lisboa, Lisbon (Portugal); Carvalho, M. R. [Universidade de Lisboa, Faculdade de Ciencias, Departamento de Geologia, Lisbon (Portugal); Antunes da Silva, M. [UNICER Bebidas, S.A, S. Mamede de Infesta (Portugal)

2013-07-15

The isotopic and chemical compositions of CO{sub 2} rich mineral waters found in the NW of Portugal were investigated. These mineral waters are mainly related to granitic and granodioritic rocks. Based on their chemical composition, two water types are distinguished (Ca-HCO{sub 3} and Ca-Na-HCO{sub 3}), indicating different underground flow paths. Through comparison with local shallow groundwaters, water chemistry indicates that the Melgaco mineral waters evolved through water-rock interaction with the hosted rocks. Stable isotope data indicates the meteoric origin of these CO{sub 2} rich mineral waters, being recharged from about 480 up to 730 m a.s.l. Considering the {delta}{sup 18}O, {delta}{sup 2}H and the hydrochemical data, no indication of mixing seems to occur between the shallow and deep groundwater systems. The {delta}{sup 13}C determinations carried out on TDIC of the CO{sub 2} rich mineral waters point to the hypothesis of methanogenesis (upper mantle CH{sub 4} source) within the system, leading to {sup 13}C enrichment. The negligible {sup 14}C content ({approx} 2 pMC) also indicates a mantle derived carbon source for the groundwater system. (author)

Direct evidence for the origin of low-18O silicic magmas: Quenched samples of a magma chamber's partially-fused granitoid walls, Crater Lake, Oregon

International Nuclear Information System (INIS)

Bacon, C.R.; Adami, L.H.; Lanphere, M.A.

1989-01-01

Partially fused granitoid blocks were ejected in the climactic eruption of Mount Mazama, which was accompanied by collapse of Crater Lake caldera. Quartz, plagioclase, and glass in the granitoids have much lower δ 18 O values (-3.4 to +4.9per mille) than any fresh lavas of Mount Mazama and the surrounding region (+5.8 to +7.0per mille). Oxygen isotope fractionation between phases in granitoids is consistent with equilibrium at T≥900deg C following subsolidus exchange with hydrothermal fluids of meteoric origin. Assimilation of ≅ 10-20% of material similar to these granitoids can account for the O and Sr isotopic compositions of lavas and juvenile pyroclasts derived from the climactic magma chamber, many of which have δ 18 O values ≅ 0.5per mille or more lower than comparable lavas of Mount Mazama. The O isotope data provide the only clear evidence for such assimilation because the mineralogy and chemical and radiogenic isotopic compositions of the granitoids (dominantly granodiorite) are similar to those of erupted juvenile magmas. The granitoid blocks from Crater Lake serve as direct evidence for the origin of 18 O depletion in large, shallow silicic magma bodies. (orig.)

99 Tc NMR determination of the oxygen isotope content in 18 O-enriched water.

Science.gov (United States)

Tarasov, Valerii P; Kirakosyan, Gayana А; German, Konstantin E

2018-03-01

99 Tc NMR has been suggested as an original method of evaluating the content of oxygen isotopes in oxygen-18-enriched water, a precursor for the production of radioisotope fluorine-18 used in positron emission tomography. To this end, solutions of NH 4 TcO 4 or NaTcO 4 (up to 0.28 mol/L) with natural abundance of oxygen isotopes in virgin or recycled 18 O-enriched water have been studied by 99 Tc NMR. The method is based on 16 O/ 17 O/ 18 O intrinsic isotope effects in the 99 Tc NMR chemical shifts, and the statistical distribution of oxygen isotopes in the coordination sphere of TcO 4 - and makes it possible to quantify the composition of enriched water by measuring the relative intensities of the 99 Tc NMR signals of the Tc 16 O 4-n 18 O n - isotopologues. Because the oxygen exchange between TcO 4 - and enriched water in neutral and alkaline solutions is characterized by slow kinetics, gaseous HCl was bubbled through a solution for a few seconds to achieve the equilibrium distribution of oxygen isotopes in the Tc coordination sphere without distortion of the oxygen composition of the water. Pertechnetate ion was selected as a probe due to its high stability in solutions and the significant 99 Tc NMR shift induced by a single 16 O→ 18 O substitution (-0.43 ± 0.01 ppm) in TcO 4 - and spin coupling constant 1 J( 99 Tc- 17 O) (131.46 Hz) favourable for the observation of individual signals of Tc 16 O 4-n 18 O n - isotopologues. Copyright © 2017 John Wiley & Sons, Ltd.

Influence of Optimization of Process Parameters on Threshold Voltage for Development of HfO2/TiSi2 18 nm PMOS

Directory of Open Access Journals (Sweden)

Atan N.

2016-01-01

Full Text Available Manufacturing a 18-nm transistor requires a variety of parameters, materials, temperatures, and methods. In this research, HfO2 was used as the gate dielectric ad TiO2 was used as the gate material. The transistor HfO2/TiSi2 18-nm PMOS was invented using SILVACO TCAD. Ion implantation was adopted in the fabrication process for the method’s practicality and ability to be used to suppress short channel effects. The study involved ion implantation methods: compensation implantation, halo implantation energy, halo tilt, and source–drain implantation. Taguchi method is the best optimization process for a threshold voltage of HfO2/TiSi2 18-nm PMOS. In this case, the method adopted was Taguchi orthogonal array L9. The process parameters (ion implantations and noise factors were evaluated by examining the Taguchi’s signal-to-noise ratio (SNR and nominal-the-best for the threshold voltage (VTH. After optimization, the result showed that the VTH value of the 18-nm PMOS device was -0.291339.

Development of an allele-specific PCR assay for simultaneous sero-typing of avian pathogenic Escherichia coli predominant O1, O2, O18 and O78 strains.

Science.gov (United States)

Wang, Shaohui; Meng, Qingmei; Dai, Jianjun; Han, Xiangan; Han, Yue; Ding, Chan; Liu, Haiwen; Yu, Shengqing

2014-01-01

Systemic infections by avian pathogenic Escherichia coli (APEC) are economically devastating to poultry industries worldwide. E. coli strains belonging to serotypes O1, O2, O18 and O78 are preferentially associated with avian colibacillosis. The rfb gene cluster controlling O antigen synthesis is usually various among different E. coli serotypes. In present study, the rfb gene clusters of E. coli serotypes O1, O2, O18 and O78 were characterized and compared. Based on the serotype-specific genes in rfb gene cluster, an allele-specific polymerase chain reaction (PCR) assay was developed. This PCR assay was highly specific and reliable for sero-typing of APEC O1, O2, O18 and O78 strains. The sensitivity of the assay was determined as 10 pg DNA or 10 colony forming units (CFUs) bacteria for serotypes O2 and O18 strains, and 500 pg DNA or 1,000 CFUs bacteria for serotypes O1 and O78 strains. Using this PCR system, APEC isolates and the infected tissue samples were categorized successfully. Furthermore, it was able to differentiate the serotypes for the samples with multi-agglutination in the traditional serum agglutination assay. Therefore, the allele-specific PCR is more simple, rapid and accurate assay for APEC diagnosis, epidemiologic study and vaccine development.

Development of an allele-specific PCR assay for simultaneous sero-typing of avian pathogenic Escherichia coli predominant O1, O2, O18 and O78 strains.

Directory of Open Access Journals (Sweden)

Shaohui Wang

Full Text Available Systemic infections by avian pathogenic Escherichia coli (APEC are economically devastating to poultry industries worldwide. E. coli strains belonging to serotypes O1, O2, O18 and O78 are preferentially associated with avian colibacillosis. The rfb gene cluster controlling O antigen synthesis is usually various among different E. coli serotypes. In present study, the rfb gene clusters of E. coli serotypes O1, O2, O18 and O78 were characterized and compared. Based on the serotype-specific genes in rfb gene cluster, an allele-specific polymerase chain reaction (PCR assay was developed. This PCR assay was highly specific and reliable for sero-typing of APEC O1, O2, O18 and O78 strains. The sensitivity of the assay was determined as 10 pg DNA or 10 colony forming units (CFUs bacteria for serotypes O2 and O18 strains, and 500 pg DNA or 1,000 CFUs bacteria for serotypes O1 and O78 strains. Using this PCR system, APEC isolates and the infected tissue samples were categorized successfully. Furthermore, it was able to differentiate the serotypes for the samples with multi-agglutination in the traditional serum agglutination assay. Therefore, the allele-specific PCR is more simple, rapid and accurate assay for APEC diagnosis, epidemiologic study and vaccine development.

Electrochemical zinc insertion into W18O49: Synthesis and characterization of new bronzes

International Nuclear Information System (INIS)

Martinez-de la Cruz, A.; Amador, U.; Rodriguez-Carvajal, J.; Garcia-Alvarado, F.

2005-01-01

Divalent zinc ions have been electrochemically inserted into W 18 O 49 , producing zinc bronzes. Under our experimental conditions, W 18 O 49 accepts zinc reversibly as a guest up to 0.9 ions per formula. The reaction seems to proceed through the formation of a solid solution in which the W-O framework of the parent oxide is maintained. The location of the Zn 2+ ions in the framework of W 18 O 49 has been determined by neutron diffraction on a chemically prepared sample having the composition Zn 0.34 W 18 O 49 . As a main result, we found that Zn prefers to insert in one of the four types of quadrangular tunnels. More precisely, it is displaced from the center to occupy a low coordination site. This result indicates that a significant covalent character exists in the Zn-O bond. - Graphical Abstract: The structure of Zn 0.36 W 18 O 49 projected along the b-axis

Sulfur isotope composition of orogenic spinel lherzolite massifs from Ariege (north-eastern pyrenees, France): An ion microprobe study

Energy Technology Data Exchange (ETDEWEB)

Chaussidon, M. (Centre de Recherches Petrographiques et Geochimiques, Vandoeuvre-les-Nancy (France)); Lorand, J. (Unite associee au CNRS, Paris (France))

1990-10-01

The orogenic spinel lherzolite massifs from Ariege, which represent tectonically emplaced fragments of the sub-continental upper mantle, are composed mainly of variously depleted peridotites. These rocks are crosscut by two generations of pyroxenites. The first is made up of layered pyroxenites, which are interpreted either as crystal segregates from Triassic continental tholeiites or as subducted parts of the oceanic crust re-injected within the upper mantle. The second consists of amphibole-rich dikes separated from Cretaceous alkali basalts. Forty sulfide grains, occurring either as inclusions within silicates or as interstitial grains, were investigated by ion microprobe for their sulfur isotopic compositions. Comparison between sulfide inclusions in silicates and interstitial sulfide grains strongly suggests that serpentinization and pyrenean metamorphism had no significant effect don the {delta}{sup 34}S values. Likewise, these values are broadly independent of the degree of partial melting. The negative {delta}{sup 34}S values of the massive peridotites could represent an ancient depletion event in the upper mantle. By contrast, the positive {delta}{sup 34}S values observed in the layered pryoxenites and the amphibole-rich dikes indicate that the two parent magmas had in common a mantle source variously enriched in {sup 34}S. Therefore, the present study reveals two extreme reservoirs characterized by different {delta}{sup 34}S values in the upper mantle. This range of variations can explain most {delta}{sup 34}S values found in MORB, continental tholeiites, and alkali basalts.

Variations in the D/H and 18O/16O ratios in cellulose extracted from a peat bog core

International Nuclear Information System (INIS)

Brenninkmeijer, C.A.M.; Mook, W.G.; Geel, B. van

1982-01-01

A peat core from a raised bog covering the period 3100 to 2400 14 C years B.P. has been analysed for D/H and 18 O/ 16 O ratios. These analyses were applied to cellulose, extracted from 56 successive layers of 1 cm thickness. D/H ratios were determined for the carbon bonded hydrogen; 18 O/ 16 O analyses were performed by applying a new method. For the interpretation of the results obtained on peat, the isotopic ratios of 11 living bog plant species were measured, showing a relatively large scatter. Most pronounced is a depletion in D of about 25per mille and in 18 O of about 5per mille of the Sphagnum mosses relative to the vascular bog plants. This different isotopic composition is reflected by the deltaD and delta 18 O records of the peat core, because the abundance of the remains of non-vascular plants is variable. If this effect is taken account of, the remaining deltaD variations appear to be too large to be attributed to variations in the isotopic compositions of precipitation. As palaeoclimatic indicators the D/H and 18 O/ 16 O ratio qualitatively agree with the pollen analytical evidence for the climatic deterioration of the Subboreal-Subatlantic transition. (orig.)

雅鲁藏布江流域降水中氧稳定同位素的时空变化%Temporal and spatial variations of δ18O in precipitation of the Yarlung Zangbo River Basin

Institute of Scientific and Technical Information of China (English)

刘忠方; 田立德; 姚檀栋; 巩同梁; 尹常亮; 余武生

2007-01-01

This paper reveals the temporal and spatial variations of stable isotope in precipitation of the Yarlung Zangbo River Basin based on the variations ofδ18O in precipitation at four stations (Lhaze, Nugesha, Yangcun and Nuxia) in 2005. The results show thatδ18O of precipitation has distinct seasonal changes in the Yarlung Zangbo River Basin. The higher value of δ18O occurs in spring prior to monsoon precipitation, and the lower value occurs during monsoon precipitation. From the spatial variations, with the altitude-effect and rainout process during moisture transport along the Yarlung Zangbo River Valley, 18O of precipitation is gradually depleted. Thus, δ18O of precipitation decreases gradually from the downstream to the upstream, and the lapse rate of δ18O in precipitation is approximately 0.34%o/100m and 0.7%o/100km for the two reasons. During monsoon precipitation, spatial variation of δ18O in precipitation is dominated by the amount effect in the large scale synoptic condition.

delta 18O variations in snow on the Devon Island ice cap, Northwest Territories, Canada

International Nuclear Information System (INIS)

Koerner, R.; Russel, R.D.

1979-01-01

A study of delta 18 O variations of snow samples taken on traverses across the Devon Island ice cap in June 1971, 1972, and 1973 has shown a difference between the accumulation conditions on the souteast and nortwest sides of the ice cap. On the souteast side there is an increasing depletion of 18 O in the snow with increasing elevation. This pattern is attibuted to the effect of orographic uplift of air masses moving over the ice cap from the southeast, which promotes condensation and precipitation due to adiabatic cooling. On the northwest side of the ice cap there is no evidence of any further depletion of 18 O in snow, neither with increasing distance from the possible moisture source in Baffin Bay to the southeast nor with increasing elevation if the air mass comes from the northwest. In this case condensation is due to isobaric cooling so that precipitation is generally from level cloud bases. The changes inferred for the isotopic composition of the water vapour as it rises up the southeast slope are found to be consistent with its depletion through precipitation under near-equilibrium conditions. It is calculated that approximately 30% of the moisture at sea level on the southeast side of the ice cap and 8% at the top of the ice cap are of local origin. Lower temporal and aerial variability of the delta values on the southeast side of the ice cap is attributed to dominance of the Baffin Bay low on that side Effecting consistency of storm conditions there. The delta values of ice in the ablation zone on the Sverdrup Glacier show the combined effect of ice movement from the accumulation to the ablation zone and climatic change during the period of movement from cold to warm and back to cold conditions again. (auth)

Regional Scale High Resolution δ18O Prediction in Precipitation Using MODIS EVI

Science.gov (United States)

Huang, Cho-Ying; Wang, Chung-Ho; Lin, Shou-De; Lo, Yi-Chen; Huang, Bo-Wen; Hatch, Kent A.; Shiu, Hau-Jie; You, Cheng-Feng; Chang, Yuan-Mou; Shen, Sheng-Feng

2012-01-01

The natural variation in stable water isotope ratio data, also known as water isoscape, is a spatiotemporal fingerprint and a powerful natural tracer that has been widely applied in disciplines as diverse as hydrology, paleoclimatology, ecology and forensic investigation. Although much effort has been devoted to developing a predictive water isoscape model, it remains a central challenge for scientists to generate high accuracy, fine scale spatiotemporal water isoscape prediction. Here we develop a novel approach of using the MODIS-EVI (the Moderate Resolution Imagining Spectroradiometer-Enhanced Vegetation Index), to predict δ18O in precipitation at the regional scale. Using a structural equation model, we show that the EVI and precipitated δ18O are highly correlated and thus the EVI is a good predictor of precipitated δ18O. We then test the predictability of our EVI-δ18O model and demonstrate that our approach can provide high accuracy with fine spatial (250×250 m) and temporal (16 days) scale δ18O predictions (annual and monthly predictabilities [r] are 0.96 and 0.80, respectively). We conclude the merging of the EVI and δ18O in precipitation can greatly extend the spatial and temporal data availability and thus enhance the applicability for both the EVI and water isoscape. PMID:23029053

{sup 18}O/{sup 16}O determination in organic matter

Energy Technology Data Exchange (ETDEWEB)

Saurer, M.; Siegwolf, R. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

1997-06-01

The oxygen isotope ratio in plant material can be used to deduce information about the climate and the environment. We present a simple and fast continuous-flow technique for the determination of the {sup 18}O/{sup 16}O ratio in organic matter. In this method the samples are thermally decomposed in the presence of glassy carbon and the evolving monoxide is used to determine the oxygen ratio. Not only cellulose but also nitrogen-containing materials can be processed when interfering gases (mainly N{sub 2}) are separated from CO by gas chromatography. (author) 2 figs., 2 refs.

Study of Factors Influencing Oxygen-18 Isotopic Contents of Dissolved Sulphate in the Shallow Groundwater In Karawang Area

International Nuclear Information System (INIS)

Ristin Pujiindiyati, E.; Bungkus Pratikno

2010-01-01

The study was conducted to investigate the factors influencing oxygen-18 isotopic contents of dissolved sulphate in shallow groundwater from Karawang area. The δ 18 O is a relative abundance of O-18 compared to O-16 in CO 2 gas. CO 2 gas was released from the equilibrium between water samples and CO 2 gas, and from the reduction of sulphate samples with graphite. From this investigation, the δ 18 O (H 2 O) values were in the range of -3.21 0 / 00 to 6.25 0 / 00 whereas the δ 18 O (SO 4 2- ) values were 9.64 0 / 00 to 20.72 0 / 00 . The wide variation of δ 18 O (SO 4 2- ) values might be result due to inhomogeneity of sulphate sources in groundwater where the groundwater sulphates were generally derived from the dissolution of marine evaporites rocks. The groundwaters and Citarum River near waters to Johar site showed lowering of δ 18 O (SO 4 2- ) values. It might be related to the present of the traditional market in this location. The lowering of these values might be due to the increase of the sulphate reduction process caused by anaerobic bacteria growth in organic garbage deposition. Plotting between δ 18 O (SO 4 2- ) and δ 18 O (H 2 O) exhibited that the oxygen contribution from H 2 O to form sulphate was less than 25%. This indicated that the shallow groundwater in Karawang is located in a non-saturated zone and had a biotic condition. (author)

Stable isotope time-series in mammalian teeth: In situ δ18O from the innermost enamel layer

Science.gov (United States)

Blumenthal, Scott A.; Cerling, Thure E.; Chritz, Kendra L.; Bromage, Timothy G.; Kozdon, Reinhard; Valley, John W.

2014-01-01

Stable carbon and oxygen isotope ratios in mammalian tooth enamel are commonly used to understand the diets and environments of modern and fossil animals. Isotope variation during the period of enamel formation can be recovered by intra-tooth microsampling along the direction of growth. However, conventional sampling of the enamel surface provides highly time-averaged records in part due to amelogenesis. We use backscattered electron imaging in the scanning electron microscope (BSE-SEM) to evaluate enamel mineralization in developing teeth from one rodent and two ungulates. Gray levels from BSE-SEM images suggest that the innermost enamel layer, <20 μm from the enamel-dentine junction, is highly mineralized early in enamel maturation and therefore may record a less attenuated isotopic signal than other layers. We sampled the right maxillary incisor from a woodrat subjected to an experimentally induced water-switch during the period of tooth development, and demonstrate that secondary ion mass spectrometry (SIMS) can be used to obtain δ18O values with 4-5-μm spots from mammalian tooth enamel. We also demonstrate that SIMS can be used to discretely sample the innermost enamel layer, which is too narrow for conventional microdrilling or laser ablation. An abrupt δ18O switch of 16.0‰ was captured in breath CO2, a proxy for body water, while a laser ablation enamel surface intra-tooth profile of the left incisor captured a δ18O range of 12.1‰. The innermost enamel profile captured a δ18O range of 15.7‰, which approaches the full magnitude of δ18O variation in the input signal. This approach will likely be most beneficial in taxa such as large mammalian herbivores, whose teeth are characterized by less rapid mineralization and therefore greater attenuation of the enamel isotope signal.

Modelling tree ring cellulose δ18O variations in two temperature-sensitive tree species from North and South America

Directory of Open Access Journals (Sweden)

A. Lavergne

2017-11-01

Full Text Available Oxygen isotopes in tree rings (δ18OTR are widely used to reconstruct past climates. However, the complexity of climatic and biological processes controlling isotopic fractionation is not yet fully understood. Here, we use the MAIDENiso model to decipher the variability in δ18OTR of two temperature-sensitive species of relevant palaeoclimatological interest (Picea mariana and Nothofagus pumilio and growing at cold high latitudes in North and South America. In this first modelling study on δ18OTR values in both northeastern Canada (53.86° N and western Argentina (41.10° S, we specifically aim at (1 evaluating the predictive skill of MAIDENiso to simulate δ18OTR values, (2 identifying the physical processes controlling δ18OTR by mechanistic modelling and (3 defining the origin of the temperature signal recorded in the two species. Although the linear regression models used here to predict daily δ18O of precipitation (δ18OP may need to be improved in the future, the resulting daily δ18OP values adequately reproduce observed (from weather stations and simulated (by global circulation model δ18OP series. The δ18OTR values of the two species are correctly simulated using the δ18OP estimation as MAIDENiso input, although some offset in mean δ18OTR levels is observed for the South American site. For both species, the variability in δ18OTR series is primarily linked to the effect of temperature on isotopic enrichment of the leaf water. We show that MAIDENiso is a powerful tool for investigating isotopic fractionation processes but that the lack of a denser isotope-enabled monitoring network recording oxygen fractionation in the soil–vegetation–atmosphere compartments limits our capacity to decipher the processes at play. This study proves that the eco-physiological modelling of δ18OTR values is necessary to interpret the recorded climate signal more reliably.

Avaliação do cumprimento da NR-18 em função do porte de obra residencial e proposta de lista de verificação da NR-18

OpenAIRE

Costella, Marcelo Fabiano; Junges, Franciele Cristina; Pilz, Silvio Edmundo

2014-01-01

O presente trabalho investiga as reais condições dos ambientes de trabalho da indústria da construção, tendo em vista os problemas relacionados à segurança do trabalho nos canteiros de obras. Formulou-se a hipótese de haver discrepância no grau de cumprimento da NR-18 em obras de diferentes portes (pequena, média e grande). Baseado em uma lista de verificação do grau de cumprimento dos requisitos da NR-18, foram avaliados 115 canteiros de obra na cidade de Chapecó - SC. Para cada item da list...

Effect of photosynthesis on the abundance of 18O13C16O in atmospheric CO2

Science.gov (United States)

Hofmann, Magdalena E. G.; Pons, Thijs L.; Ziegler, Martin; Lourens, Lucas J.; Röckmann, Thomas

2016-04-01

The abundance of the isotopologue 18O13C16O (Δ47) in atmospheric air is a promising new tracer for the atmospheric carbon cycle (Eiler and Schauble, 2004; Affek and Eiler, 2006; Affek et al., 2007). The large gross fluxes in CO2 between the atmosphere and biosphere are supposed to play a major role in controlling its abundance. Eiler and Schauble (2004) set up a box model describing the effect of air-leaf interaction on the abundance of 18O13C16O in atmospheric air. The main assumption is that the exchange between CO2 and water within the mesophyll cells will imprint a Δ47 value on the back-diffusing CO2 that reflects the leaf temperature. Additionally, kinetic effects due to CO2 diffusion into and out of the stomata are thought to play a role. We investigated the effect of photosynthesis on the residual CO2 under controlled conditions using a leaf chamber set-up to quantitatively test the model assumptions suggested by Eiler and Schauble (2004). We studied the effect of photosynthesis on the residual CO2 using two C3 and one C4 plant species: (i) sunflower (Helianthus annuus), a C3 species with a high leaf conductance for CO2 diffusion, (ii) ivy (Hedera hibernica), a C3 species with a low conductance, and (iii), maize (Zea mays), a species with the C4 photosynthetic pathway. We also investigated the effect of different light intensities (photosynthetic photon flux density of 200, 700 and 1800 μmol m2s-1), and thus, photosynthetic rate in sunflower and maize. A leaf was mounted in a cuvette with a transparent window and an adjustable light source. The air inside was thoroughly mixed, making the composition of the outgoing air equal to the air inside. A gas-mixing unit was attached at the entrance of the cuvette that mixed air with a high concentration of scrambled CO2 with a Δ47 value of 0 to 0.1‰ with CO2 free air to set the CO2 concentration of ingoing air at 500 ppm. The flow rate through the cuvette was adjusted to the photosynthetic activity of the leaf

Use of N stable isotope and microbial analyses to define wastewater influence in Mobile Bay, AL

Energy Technology Data Exchange (ETDEWEB)

Daskin, Joshua H. [MB 0193 Brandeis University, Waltham, MA 02454 (United States); Calci, Kevin R.; Burkhardt, William [1 Iberville Road, US Food and Drug Administration Gulf Coast Seafood Laboratory, Dauphin Island, AL 36528 (United States); Carmichael, Ruth H. [101 Bienville Boulevard, Dauphin Island Sea Lab, Dauphin Island, AL 36528 (United States); University of South Alabama, Mobile, AL, 36688 (United States)], E-mail: rcarmichael@disl.org

2008-05-15

We assessed short-term ecological and potential human health effects of wastewater treatment plant (WTP) effluent by measuring {delta}{sup 15}N per mille and microbial concentrations in oysters and suspended particulate matter (SPM). We also tested male-specific bacteriophage (MSB) as an alternative to fecal coliforms, to assess potential influence of wastewater contamination on shellfish. WTP effluent did not affect oyster growth or survival, but SPM and oysters acquired wastewater-specific {delta}{sup 15}N per mille . {delta}{sup 15}N values were depleted near the WTP, typical of low-level processed wastewater. Fecal coliform and MSB concentrations were higher in samples taken closest to the WTP, and MSB values were significantly correlated with {delta}{sup 15}N per mille in oyster tissues. Overall, oysters demonstrated relatively rapid integration and accumulation of wastewater-specific {delta}{sup 15}N per mille and indicator microorganisms compared to water samples. These data suggest oysters were superior sentinels compared to water, and MSB was a more reliable indicator of wastewater influence on shellfish than fecal coliforms.

Standardized uptake values of fluorine-18 fluorodeoxyglucose: the value of different normalization procedures

International Nuclear Information System (INIS)

Schomburg, A.; Bender, H.; Reichel, C.; Sommer, T.; Ruhlmann, J.; Kozak, B.; Biersack, H.J.

1996-01-01

While the evident advantages of absolute metabolic rate determinations cannot be equalled by static image analysis of fluorine-18 fluorodexyglucose positron emission tomographic (FDG PET) studies, various algorithms for the normalization of static FDG uptake values have been proposed. This study was performed to compare different normalization procedures in terms of dependency on individual patient characteristics. Standardized FDG uptake values (SUVs) were calculated for liver and lung tissue in 126 patients studied with whole-body FDG PET. Uptake values were normalized for total body weight, lean body mass and body surface area. Ranges, means, medians, standard deviations and variation coefficients of these SUV parameters were calculated and their interdependency with total body weight, lean body mass, body surface area, patient height and blood sugar levels was calculated by means of regression analysis. Standardized FDG uptake values normalized for body surface area were clearly superior to SUV parameters normalized for total body weight or lean body mass. Variation and correlation coefficients of body surface area-normalized uptake values were minimal when compared with SUV parameters derived from the other normalization procedures. Normalization for total body weight resulted in uptake values still dependent on body weight and blood sugar levels, while normalization for lean body mass did not eliminate the positive correlation with lean body mass and patient height. It is concluded that normalization of FDG uptake values for body surface area is less dependent on the individual patient characteristics than are FDG uptake values normalized for other parameters, and therefore appears to be preferable for FDG PET studies in oncology. (orig.)

INVESTIGATION OF STABLE ISOTOPE OF 18O AND 2H IN SHALLOW GROUNDWATER FROM KARAWANG AREA

Directory of Open Access Journals (Sweden)

E. Ristin Pujiindiyati

2010-06-01

Full Text Available Karawang area is well known as an agriculture area and 2% area is utilized for industries. Clean water demands increase due to developing industry development and population increasement. The origin of groundwater is necessary to keep the sustainability of water resources in this area. Stable isotopes such as 18O and 2H can be used as a parameter to trace the ground water origin. The methods used were Epstein-Mayeda and Zinc reduction for analysis 18O and 2H, respectively. Sampling period was conducted in major dry season in year 2002. The result showed that evaporation effect had influenced to the content of both isotopes in its shallow groundwater that caused a slope shift from its local meteoric line. The origin of its shallow groundwater was from rainwater infiltrating directly in less than 10 m altitude. Citarum River showed more depleted values in both isotopes compared to shallow groundwater and it indicated that its water might originate from spring at the altitude of 600 m.     Keywords: oxygene-18, deuterium, groundwater, isotope

Simulation and optimization of stable isotope 18O separation by cascade distillation

International Nuclear Information System (INIS)

Jiang Yongyue; Chen Yuyan; Qin Chuanjiang; Liu Yan; Gu Hongsen

2011-01-01

The research about started from the plan of four cascade towers design was carried. Firstly, the method of experiment design was using uniform design. Then the incidence formula with the method of binomial stepwise regression was gotten. Last, the optimal operation conditions were gotten by using the method of genetic algorithm. Considering comprehensive factors of drawn from feed rate and from flow rates between cascade column, conclusions were reached on the study of the impact on the abundance of the isotope 18 O. Finally, the incidence formula between the abundance of the isotope 18 O and four operating variables were gotten. Also the incidence formula between heat consumption of the isotope 18 O and four operating variables were gotten. Besides, single factor response diagram of four factors were shown at last. The results showed that the method of simulation and optimization could be applied to 18 O industrial design and would be popular in traditional distillation process to realize optimization design. (authors)

Effects of recharge and discharge on delta2H and delta18O composition and chloride concentration of high arsenic/fluoride groundwater from the Datong Basin, northern China.

Science.gov (United States)

Xie, Xianjun; Wang, Yanxin; Su, Chunli; Duan, Mengyu

2013-02-01

To better understand the effects of recharge and discharge on the hydrogeochemistry of high levels of arsenic (As) and fluoride (F) in groundwater, environmental isotopic composition (delta2H and delta18O) and chloride (Cl) concentrations were analyzed in 29 groundwater samples collected from the Datong Basin. High arsenic groundwater samples (As > 50 micog/L) were found to be enriched in lighter isotopic composition that ranged from -92 to -78 per thousand for deuterium (delta2H) and from -12.5 to -9.9 per thousand for oxygen-18 (delta18O). High F-containing groundwater (F > 1 mg/L) was relatively enriched in heavier isotopic composition and varied from -90 to -57 per thousand and from -12.2 to -6.7 per thousand for delta2H and delta18O, respectively. High chloride concentrations and delta18O values were primarily measured in groundwater samples from the northern and southwestern portions of the study area, indicating the effect of evaporation on groundwater. The observation of relatively homogenized and low delta18O values and chloride concentrations in groundwater samples from central part of the Datong Basin might be a result of fast recharge by irrigation returns, which suggests that irrigation using arsenic-contaminated groundwater affected the occurrence of high arsenic-containing groundwater in the basin.

Preparation of aligned W{sub 18}O{sub 49} nanowire clusters with high photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Zhang, Ning [State Key Laboratory of Inorganic Synthesis & Preparative Chemistry, Jilin University, Changchun 130012 (China); Zhao, Yafei, E-mail: zhaoyafei007@126.com [State Key Laboratory of Inorganic Synthesis & Preparative Chemistry, Jilin University, Changchun 130012 (China); School of Chemical Engineering and Energy, Zhengzhou University, Zhengzhou, Henan 450001 (China); Lu, Yanjie [School of Chemical Engineering and Energy, Zhengzhou University, Zhengzhou, Henan 450001 (China); Zhu, Guangshan, E-mail: zhugs@jlu.edu.cn [State Key Laboratory of Inorganic Synthesis & Preparative Chemistry, Jilin University, Changchun 130012 (China)

2017-04-15

Highlights: • Aligned W{sub 18}O{sub 49} nanowire clusters were prepared by a facile hydrothermal method. • W{sub 18}O{sub 49} has unique structure, high degree of crystallinity and large surface area. • W{sub 18}O{sub 49} nanowire clusters exhibited high photocatalytic degradation activity. - Abstract: The aligned W{sub 18}O{sub 49} nanowire clusters were synthesized via a facile and economic ethanol-assisted hydrothermal method using peroxopolytungstic acid as precursor. Results show that the as-prepared W{sub 18}O{sub 49} exhibits a high yield and ultrathin structure with preferential growth direction along [0 1 0]. The amount of peroxopolytungstic acid and reaction time play significant role on the morphology of W{sub 18}O{sub 49} nanowires. The nanowires have unique structure, high degree of crystallinity, large specific surface area, and large number of defects such as oxygen vacancies, which are responsible for their high photocatalytic performance for degradation of methylene blue. The photocatalytic conversion of methylene blue can reach above 98% after degradation. W{sub 18}O{sub 49} also exhibits good photodegradation stability after five cycles of reuse. The results demonstrate that the as-prepared W{sub 18}O{sub 49} nanowire clusters are expected to be a promising material for applications in the field of environment.

δ18O analysis of individual carbohydrates - a new method for GC-pyrolysis-IRMS

Science.gov (United States)

Lehmann, Marco M.; Fischer, Maria; Zech, Michael; Siegwolf, Rolf T. W.; Saurer, Matthias

2015-04-01

Measuring the oxygen isotopic composition (δ18O) of various plant tissues is a widely used tool to investigate biochemical and physiological processes. While we have a good understanding about the hydrological cycle in plants with an evaporative enrichment in 18O in leaf water, we still lack knowledge about the biochemical link between the oxygen atoms in leaf water, leaf assimilates, and stem cellulose and associated isotope fractionations. Especially, the influence of different environmental factors on δ18O of individual carbohydrates (i.e. sugars) and thus on δ18O of cellulose is not fully resolved. A better understanding of these processes may improve climatic reconstructions of tree-ring studies about past environmental conditions. However, further progress in this topic is limited since a precise and reliable method to determine δ18O of individual sugars has not been available yet. With our new approach we attempt to overcome this issue by establishing a new methylation derivatization method suitable for GC-pyrolysis -IRMS. A methyl group (CH3) was thereby added to all hydroxyl groups of a sugar (e.g., glucose, fructose, and sucrose) during a catalyzed one-pot reaction overnight in acetonitrile with methyl iodide (CH3-I) and silver oxide, making them amenable for GC analysis. First results show a very good precision for δ18O of sucrose, but also δ18O of other high-abundant sugars such as glucose and fructose could be measured for the first time. We successfully analyzed a standard mix of all three sugars and determined various other carbohydrates not only related to plant sciences (e.g. mannitol, lactose), showing promising δ18O results. First tests with real plant samples were performed to make this method available for determining δ18O of individual carbohydrates of diverse plant tissues. In future, this new methylation derivatization method should allow us analyzing plant samples of different field sites and of lab experiments to investigate the

Observation of Isotope Ratios (δ2H, δ18O, 87Sr/86Sr) of Tap Water in Urban Environments

Science.gov (United States)

Mancuso, C. J.; Tipple, B. J.; Ehleringer, J. R.

2014-12-01

Urban environments are centers for rapidly growing populations. In order to meet the culinary water needs of these areas, municipal water departments use water from multiple locations and/or sources, often piped differentially to different locations within a municipality. This practice creates isotopically distinct locations within an urban area and therefore provides insight to urban water management practices. In our study we selected urban locations in the Salt Lake Valley, UT (SLV) and San Francisco Bay Area, CA (SFB) where we hypothesized geographically distinct water isotopic ratio differences existed. Within the SLV, municipal waters come from the same mountainous region, but are derived from different geologically distinct watersheds. In contrast, SFB waters are derived from regionally distinct water sources. We hypothesized that the isotope ratios of tap waters would differ based upon known municipal sources. To test this, tap water samples were collected throughout the urban regions in SLV and SFB and analyzed for δ2H, δ18O and 87Sr/86Sr isotope ratios. Seasonal collections were also made to assess if isotope ratios differed throughout the year. Within SLV and SFB, different regions were characterized by distinct paired δ18O and 87Sr/86Sr values. These different realms also agreed with known differences in municipal water supplies within the general geographic region. Waters from different cities within Marin County showed isotopic differences, consistent with water derived from different local reservoirs. Seasonal variation was observed in paired δ18O and 87Sr/86Sr values of tap water for some locations within SLV and SFB, indicating management decisions to shift from one water source to another depending on demand and available resources. Our study revealed that the δ18O and 87Sr/86Sr values of tap waters in an urban region can exhibit significant differences despite close spatial proximity if districts differ in their use of local versus

Comparative study of the elastic scattering of 178.4 MeV antiprotons by the 16O and 18O isotopes

International Nuclear Information System (INIS)

Bruge, G.; Chaumeaux, A.; Birien, P.; Drake, D.M.; Garreta, D.; Janouin, S.; Legrand, D.; Lemaire, M.C.; Mayer, B.; Pain, J.; Peng, J.C.

1986-01-01

Elastic scattering of 178.4 MeV anti p has been measured on 16 O and 18 O isotopes. Both macroscopic and microscopic analyses of the data show differences which can be related to the neutron excess in 18 O. (orig.)

Seasonal and interannual variability of the Mid-Holocene East Asian monsoon in coral δ18O records from the South China Sea

Science.gov (United States)

Sun, Donghuai; Gagan, Michael K.; Cheng, Hai; Scott-Gagan, Heather; Dykoski, Carolyn A.; Edwards, R. Lawrence; Su, Ruixia

2005-08-01

Understanding the full range of past monsoon variability, with reference to specific monsoon seasons, is essential to test coupled climate models and improve their predictive capabilities. We present a 54-year long, high-resolution skeletal oxygen isotope (δ18O) record extracted from a well-preserved, massive Porites sp. coral at Hainan Island, South China Sea, to investigate East Asian monsoon variability during summer and winter ∼4400 calendar yr ago. Analysis of modern coral δ18O confirms that Porites from Hainan Island are well positioned to record winter monsoon forcing of sea surface temperature (SST), as well as the influence of summer monsoon rainfall on sea surface salinity (SSS). The coral record for ∼4400 yr ago shows ∼9% amplification of the annual cycle of δ18O, in good agreement with coupled ocean-atmosphere models showing higher summer rainfall (lower coral δ18O) and cooler winter SSTs (higher coral δ18O) in response to greater Northern Hemisphere insolation seasonality during the Middle Holocene. Mean SSTs in the South China Sea during the Mid-Holocene were within 0.5 °C of modern values, yet the mean δ18O for the fossil coral is ∼0.6‰ higher than that for the modern coral, suggesting that the δ18O of surface seawater was higher by at least ∼0.5‰, relative to modern values. The 18O-enrichment is likely to be driven by greater advection of moisture towards the Asian landmass, enhanced monsoon wind-induced evaporation and vertical mixing, and/or invigorated advection of saltier 18O-enriched Pacific water into the relatively fresh South China Sea. The 18O-enrichment of the northern South China Sea ∼4400 yr ago contributes to mounting evidence for recent freshening of the tropical Western Pacific. Today, winter SST and summer SSS variability in the South China Sea reflect the interannual influence of ENSO and the biennial variability inherent to monsoon precipitation. Spectral analysis of winter SSTs ∼4400 yr ago reveals a

Evidence of prehistoric Lapita diet at Watom Island, Papua New Guinea, using stable isotopes

Energy Technology Data Exchange (ETDEWEB)

Leach, B F [Archaeozoology Laboratory, Museum of New Zealand, Wellington (New Zealand); Quinn, C J [178 Queen Street North, Dunedin (New Zealand); Lyon, G L [Institute of Geological and Nuclear Sciences Ltd., Lower Hutt (New Zealand); Haystead, A [Auckland Institute of Technology, Auckland (New Zealand); Myers, D B [Wellcome Medical Research Institute, Otago Medical School, Dunedin (New Zealand)

1998-07-01

Samples of human bone from six individuals from the Lapita burial ground at Reber-Rakival on Watom Island in New Britain were analysed for {delta}{sup 13}C, {delta}{sup 15}N, and {delta}{sup 34}/S. The mean values obtained were -18.1, 11.6 and 9.9 respectively. From existing knowledge of isotope values, calorific content and protein yields for the main Pacific food types, computer simulation was used to randomly generate a large number of possible food compositions, in order to find the type of diet which could have produced the isotope pattern at Watom. The simulation produced solutions which are within acceptable limits of the Watom isotope signature. The mean food composition per day was then estimated. This analysis shows that approximately 64% of the diet at Watom came from land-based foods and 36% from the sea. Plant foods contributed 53% per weight. It is notable that C4 plants were present in the diet. There are two possible sources of this - sugar cane, Saccharum officinarum, and/or a herbivore which browsed on the C4 grasslands of Papua New Guinea, such as Saccharum spontaneum (pit-pit) and Imperata cylindrica (kunai). Fish and land herbivores are the main sources of protein in the Watom diet, while plant foods contributed by far the most food energy. (author). 20 refs., 2 figs., 3 tabs.

Clinical value of 18F-fluorodihydroxyphenylalanine positron emission tomography/computed tomography (18F-DOPA PET/CT) for detecting pheochromocytoma

International Nuclear Information System (INIS)

Luster, Markus; Zeich, Katrin; Glatting, Gerhard; Buck, Andreas K.; Solbach, Christoph; Reske, Sven N.; Karges, Wolfram; Pauls, Sandra; Verburg, Frederik A.; Dralle, Henning; Neumaier, Bernd; Mottaghy, Felix M.

2010-01-01

In detecting pheochromocytoma (PHEO), positron emission tomography (PET) with the radiolabelled amine precursor 18 F-fluorodihydroxyphenylalanine ( 18 F-DOPA) offers excellent specificity, while computed tomography (CT) provides high sensitivity and ability to localize lesions; therefore, the combination of these modalities could be advantageous in this setting. The aim of this study was to investigate whether combined 18 F-DOPA PET/CT more accurately detects and localizes PHEO lesions than does each modality alone. 18 F-DOPA PET, CT and 18 F-DOPA PET/CT images of 25 consecutive patients undergoing diagnostic scanning of suspected sporadic or multiple endocrine neoplasia type 2 syndrome-associated PHEO were reviewed retrospectively in randomized sequence. Two blinded observers scored the images regarding the likelihood of PHEO being present and localizable. Results were correlated with subsequent clinical history and, when available, histology. Of the 19 lesions detected by all three modalities, PET identified each as positive for PHEO, but was unable to definitively localize 15 of 19 (79%). CT could definitively localize all 19 lesions, but could not definitively diagnose or exclude PHEO in 18 of 19 (95%) lesions. Furthermore, CT falsely identified as negative for PHEO one lesion which was judged to be positive for this tumor by both PET and PET/CT. Only in PET/CT scans were all 19 lesions accurately characterized and localized. On a per-patient basis, the sensitivity of 18 F-DOPA PET/CT for PHEO was 100% and the specificity 88%, with a 100% positive predictive value and an 88% negative predictive value. 18 F-DOPA PET/CT more accurately diagnoses and localizes adrenal and extra-adrenal masses suspicious for PHEO than do 18 F-DOPA PET or CT alone. (orig.)

Stable isotopes (2H, 18O and 13C) in groundwaters from the northwestern portion of the Guarani Aquifer System (Brazil)

Science.gov (United States)

Gastmans, Didier; Chang, Hung Kiang; Hutcheon, Ian

2010-09-01

The groundwater flow pattern of the western part of the Guarani Aquifer System (GAS), Brazil, is characterized by three regional recharge areas in the north, and a potentiometric divide in the south, which trends north-south approximately. Groundwater flow is radial from these regional recharge areas toward the center of Paraná Sedimentary Basin and toward the western outcrop areas at the border of the Pantanal Matogrossense, because of the potentiometric divide. The isotopic composition of GAS groundwater leads to understanding the paleoclimatic conditions in the regional recharge areas. The δ18O and δ2H isotopic ratios of GAS groundwaters vary, respectively, from -9.1 to -4.8‰ V-SMOW and -58.4 to -21.7‰ V-SMOW. In the recharge zones, enriched δ18O values are observed, while in the confined zone lighter δ18O values are observed. These suggest that climatic conditions were 10°C cooler than the present during the recharge of these waters. The δ13C ratios in groundwater of GAS, in the study area, vary from -19.5 to -6.5‰ VPDB, increasing along the regional flow lines toward the confined zone. This variation is related to dissolution of carbonate cement in the sandstones.

Automated simultaneous measurement of the δ(13) C and δ(2) H values of methane and the δ(13) C and δ(18) O values of carbon dioxide in flask air samples using a new multi cryo-trap/gas chromatography/isotope ratio mass spectrometry system.

Science.gov (United States)

Brand, Willi A; Rothe, Michael; Sperlich, Peter; Strube, Martin; Wendeberg, Magnus

2016-07-15

The isotopic composition of greenhouse gases helps to constrain global budgets and to study sink and source processes. We present a new system for high-precision stable isotope measurements of carbon, hydrogen and oxygen in atmospheric methane and carbon dioxide. The design is intended for analyzing flask air samples from existing sampling programs without the need for extra sample air for methane analysis. CO2 and CH4 isotopes are measured simultaneously using two isotope ratio mass spectrometers, one for the analysis of δ(13) C and δ(18) O values and the second one for δ(2) H values. The inlet carousel delivers air from 16 sample positions (glass flasks 1-5 L and high-pressure cylinders). Three 10-port valves take aliquots from the sample stream. CH4 from 100-mL air aliquots is preconcentrated in 0.8-mL sample loops using a new cryo-trap system. A precisely calibrated working reference air is used in parallel with the sample according to the Principle of Identical Treatment. It takes about 36 hours for a fully calibrated analysis of a complete carousel including extractions of four working reference and one quality control reference air. Long-term precision values, as obtained from the quality control reference gas since 2012, account for 0.04 ‰ (δ(13) C values of CO2 ), 0.07 ‰ (δ(18) O values of CO2 ), 0.11 ‰ (δ(13) C values of CH4 ) and 1.0 ‰ (δ(2) H values of CH4 ). Within a single day, the system exhibits a typical methane δ(13) C standard deviation (1σ) of 0.06 ‰ for 10 repeated measurements. The system has been in routine operation at the MPI-BGC since 2012. Consistency of the data and compatibility with results from other laboratories at a high precision level are of utmost importance. A high sample throughput and reliability of operation are important achievements of the presented system to cope with the large number of air samples to be analyzed. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

Measurements of the 18O/16O ratio of dissolved oxygen in the North Sea during FLEX 76

International Nuclear Information System (INIS)

Foerstel, H.; Zielke, H.

1978-01-01

In spring 1976 a special part of the North Sea was the subject of research by a group of international scientists in the so-called 'Fladenground Experiment 1976 (FLEX 76). The team participated aboard the research ship Planet in an attempt to study the oxygen exchange between sea and atmosphere and the mixing within the water column. The water samples were taken in a small area during a period of two weeks. The water depth did not exceed 140 m. The dissolved oxygen was extracted using a vacuum system, and stored after adsorption on a molecular sieve. In the laboratory the oxygen was burned to carbon dioxide and the 18 O/ 16 O ratio was determined with a mass spectrometer. At the surface the sea water was saturated with air and showed the 18 O/ 16 O ratio of atmospheric oxygen. Towards the deeper layers the oxygen was consumed, and as a result the heavier isotope 18 O was enriched. This enrichment can be seen in a very marked manner even in the upper 100 m of the sea. In our case the 18 O enrichment indicates that the mixing processes did not exchange the oxygen of the layers beneath the surface rapidly. (Auth.)

Investigations of the ratios of stable carbon isotopes in atmospheric relevant VOC using simulation and field experiments; Untersuchungen der Verhaeltnisse stabiler Kohlenstoffisotope in atmosphaerisch relevanten VOC in Simulations- und Feldexperimenten

Energy Technology Data Exchange (ETDEWEB)

Spahn, Holger

2010-07-01

Volatile organic compounds (VOC) play an important role in the regional and global atmospheric chemistry. The author of the contribution under consideration reports on the analysis of the ratios of stable carbon isotopes ({delta}({sup 13}C) analysis) in atmospheric VOCs. At first, the state of the art of this analytical technique is described. For the first time {delta}({sup 13}C) values of different monoterpenes have been determined in the investigation of vegetable emissions at a plant chamber. By means of the oxidation of {beta}-pinene by ozone in an aerosol chamber, the kinetic isotope effect of this reaction was determined. In southern Germany, air samples for the {delta}({sup 13}C) analysis were collected using a zeppelin. This enables a height-resolved measurement of {delta}({sup 13}C) values. Based on these measurements, the average photochemical age for methanol, toluene and p-xylene at different heights was calculated.

The value of 18F-FDG PET/CT in diagnosing infectious endocarditis

International Nuclear Information System (INIS)

Kouijzer, Ilse J.E.; Vos, Fidel J.; Janssen, Marcel J.R.; Dijk, Arie P.J. van; Oyen, Wim J.G.; Bleeker-Rovers, Chantal P.

2013-01-01

Early detection of infectious endocarditis is challenging. For diagnosing infectious endocarditis, the revised Duke criteria are the gold standard. Evidence of endocardial involvement on echocardiography is a major criterion, but sensitivity and specificity of echocardiography are not optimal. Here we investigated the utility of 18 F-fluorodeoxyglucose (FDG) positron emission tomography and computed tomography (PET/CT) to diagnose infectious endocarditis in patients with gram-positive bacteraemia. Seventy-two patients with gram-positive bacteraemia were prospectively included. Patients with a positive blood culture growing Staphylococcus aureus, Streptococcus species or Enterococcus species were eligible when a risk factor for developing metastatic infectious foci was present. Infectious endocarditis was defined according to the revised Duke criteria. All patients underwent 18 F-FDG PET/CT and echocardiography. 18 F-FDG uptake in or around the heart valves was evaluated independently by two nuclear medicine physicians. Sensitivity for diagnosing infectious endocarditis with 18 F-FDG PET/CT was 39 % and specificity was 93 %. The positive predictive value was 64 % and negative predictive value was 82 %. The mortality rate in patients without infectious endocarditis and without increased 18 F-FDG uptake in or around the heart valves was 18 %, and in patients without infectious endocarditis but with high 18 F-FDG uptake in or around the heart valves the mortality rate was 50 % (p = 0.181). 18 F-FDG PET/CT is currently not sufficiently adequate for the diagnosis of infectious endocarditis because of its low sensitivity. Improvements such as patient preparation with low carbohydrate-fat allowed diet and technical advances in the newest PET/CT scanners may increase sensitivity in future studies. (orig.)

Evidence for a universal pathway of abscisic acid biosynthesis in higher plants from 18O incorporation patterns

International Nuclear Information System (INIS)

Zeevaart, J.A.D.; Heath, T.G.; Gage, D.A.

1989-01-01

Previous labeling studies of abscisic acid (ABA) with 18 O 2 have been mainly conducted with water-stressed leaves. In this study, 18 O incorporation into ABA of stressed leaves of various species was compared with 18 O labeling of ABA of turgid leaves and of fruit tissue in different stages of ripening. In stressed leaves of all six species investigated, avocado (Persea americana), barley (Hordeum vulgare), bean (Phaseolus vulgaris), cocklebur (Xanthium strumarium), spinach (Spinacia oleracea), and tobacco (Nicotiana tabacum), 18 O was most abundant in the carboxyl group, whereas incorporation of a second and third 18 O in the oxygen atoms on the ring of ABA was much less prominent after 24 h in 18 O 2 . ABA from turgid bean leaves showed significant 18 O incorporation, again with highest 18 O enrichment in the carboxyl group. On the basis of 18 O-labeling patterns observed in ABA from different tissues it is concluded that, despite variations in precusor pool sizes and intermediate turnover rates, there is a universal pathway of ABA biosynthesis in higher plants which involves cleavage of a larger precursor molecule, presumably an oxygenated carotenoid

Monitoring of a fast-growing speleothem site from the Han-sur-Lesse cave, Belgium, indicates equilibrium deposition of the seasonal δ18O and δ13C signals in the calcite

Science.gov (United States)

Van Rampelbergh, M.; Verheyden, S.; Allan, M.; Quinif, Y.; Keppens, E.; Claeys, P.

2014-10-01

Speleothems provide paleoclimate information on multimillennial to decadal scales in the Holocene. However, seasonal or even monthly resolved records remain scarce. Such records require fast-growing stalagmites and a good understanding of the proxy system on very short timescales. The Proserpine stalagmite from the Han-sur-Less cave (Belgium) displays well-defined/clearly visible darker and lighter seasonal layers of 0.5 to 2 mm thickness per single layer, which allows a measuring resolution at a monthly scale. Through a regular cave monitoring, we acquired a good understanding of how δ18O and δ13C signals in modern calcite reflect climate variations on the seasonal scale. From December to June, outside temperatures are cold, inducing low cave air and water temperature, and bio-productivity in the soil is limited, leading to lower pCO2 and higher δ13C values of the CO2 in the cave air. From June to December, the measured factors display an opposite behavior. The absence of epikarst water recharge between May and October increases prior calcite precipitation (PCP) in the vadose zone, causing drip water to display increasing pH and δ13C values over the summer months. Water recharge of the epikarst in winter diminishes the effect of PCP and as a result the pH and δ13C of the drip water gradually decrease. The δ18O and δ13C signals of fresh calcite precipitated on glass slabs also vary seasonally and are both reflecting equilibrium conditions. Lowest δ18O values occur during the summer, when the δ13C values are high. The δ18O values of the calcite display seasonal variations due to changes in the cave air and water temperature. The δ13C values reflect the seasonal variation of the δ13CDIC of the drip water, which is affected by the intensity of PCP. This same anticorrelation of the δ18O versus the δ13C signals is seen in the monthly resolved speleothem record that covers the period between 1976 and 1985 AD. Dark layers display lower δ18O and higher δ13C

Factors controlling the compositional variations among the marine and non-marine black shales from Egypt

Energy Technology Data Exchange (ETDEWEB)

Baioumy, Hassan M. [Central Metallurgical R and D Institute, PO Box 87 Helwan, Cairo (Egypt); Ismael, Ismael S. [Faculty of Science, Suez Canal University, Suez (Egypt)

2010-07-01

Index of Alteration (CIA) values in the non-marine black shales compared to the marine black shales suggest a prevailing of more intensive weathering conditions during the Jurassic time in Egypt compared to the Cretaceous. Higher weathering of non-marine shales is compatible with a higher zircon and TiO{sub 2} contents. The higher zircon may account for some of the differences on the contents and mode of occurrence of elements found between the marine and non-marine shales, such as the higher REEs, Nb, Y, and Hf. The higher C{sub org} and Ni/Co, V/Cr, and U/Al ratios in the Red Sea black shales are attributed to more reducing depositional environment of these shales. Marine organic matter seems to be responsible for the selective fixation of some trace elements such as Cr, V, and Zn. Sulfur isotopes from pyrite suggest a marine origin of this pyrite in all shales. However, variations in the {delta}{sup 34}S values reflect variations in the depositional settings. {delta}{sup 34}S data suggest a sulphate-replete (open) system for the pyrite in the Red Sea and lower member (Duwi Formation) of Abu Tartur black shales, sulphate-limited (closed) system in a brackish setting for the Maghara black shales, and coastal plain setting in the middle member of Abu Tartur area. The similarities among marine and non-marine black shales such as positive correlations between Zr and both Nb and Hf as well as between Fe{sub 2}O{sub 3} and Co might reflect the geochemical behaviors of such elements rather than variations in the provenances and/or depositional environments. (author)

Late Pleistocene Vegetation, Climate and Relative Sea Level Changes in the Southeastern Brazilian Coast, Based on C and N Isotopes and Bio Indicator Analysis of Mangrove Organic Matter

Energy Technology Data Exchange (ETDEWEB)

Pessenda, L. C.R.; Vidotto, E.; Buso, Jr., A. A.; Assarini, Jr., J. P.; Bendassollia, J. A. [Center for Nuclear Energy in Agriculture (CENA), University of Sao Paulo (USP), Piracicaba, Sao Paulo (Brazil); De Oliveira, P. E. [University of Guarulhos (UNG), Guarulhos, Sao Paulo (Brazil); Macias, F. [' ' Luiz de Queiroz' ' College of Agriculture/USP, Piracicaba, Sao Paulo (Brazil); Ricardi-Branco, F. [University of Campinas - Geosciences Institute, Campinas, Sao Paulo (Brazil)

2013-07-15

On the southeastern Brazilian coast, mangrove organic matter records have been studied by C and N isotopes, pollen and diatom analysis to reconstruct 40 ka of vegetation and climatic history. The {delta}{sup 13}C and {delta}{sup 15}N presented more depleted values from 40 to 19 ka BP. The high C/N ratios and depleted isotopic values indicate the predominance of C3 land plants in the location presently occupied by the mangrove vegetation, and a lower sea level than today. The presence of pollen of Ilex, Weinmannia, Symplocos, Drimys and Podocarpus suggest a colder and more humid climate than present. From 19 to 2.2 ka BP a sedimentary hiatus is associated with a sea level rise. The presence of mangrove in its present position since at least 2.200 a BP and the return of the marine coastline are associated with the lowest C/N ratio, more enriched {delta}{sup 13}C and {delta}{sup 15}N values and the presence of marine diatoms. (author)

The evaluation and calculation of production cross sections of {sup 18}F, {sup 77}Br and {sup 186}Re medical radioisotopes from {sup 18}O, {sup 77}Se and {sup 186}W(p,n) reactions up to 80 MeV

Energy Technology Data Exchange (ETDEWEB)

Youxiang, Zhuang [Chinese Nuclear Data Center, Beijing, BJ (China)

1996-06-01

The medical radioisotopes are used for diagnostic and therapeutic purposes, as well as metabolism and physiological function researches in modern medicine. The major applications are of functional imaging using PET agents for {sup 18}F, various therapeutic pharmaceuticals via auger electrons for {sup 77}Br, cancers diagnosis and therapy for {sup 186}Re. The evaluations of experimental data and theoretical calculations for {sup 18}O, {sup 77}Se, {sup 187}W(p,n) reactions up to 80 MeV are presented and analysed. The recommended values for {sup 18}O(p,n){sup 18}F, {sup 77}Se(p,n){sup 77}Br and {sup 186}W(p,n){sup 186}Re reaction cross sections are given. (6 figs.).

Complete Measurement of Stable Isotopes in N2O (δ15N, δ15Nα, δ15Nβ, δ18O, δ17O) Using Off-Axis Integrated Cavity Output Spectroscopy (OA-ICOS)

Science.gov (United States)

Leen, J. B.; Gupta, M.

2014-12-01

nitrate in soil and groundwater and may be used to differentiate other sources of nitrate for which the range of Δ17O values is much smaller. By measuring δ15N, δ15Nα, δ15Nβ, δ18O and δ17O, our instrument will help researchers unravel the complicated nitrate mixing problem to determine the sources and sinks of nitrate pollution.

Elastic and inelastic scattering of the 14C + 18O nuclei

Directory of Open Access Journals (Sweden)

A. T. Rudchik

2010-12-01

Full Text Available New angular-distribution data of 14С + 18О elastic and inelastic scattering at the energy Elab(18O = 105 MeV were obtained firstly. The data were analysed within the optical model and coupled-reaction-channels methods including contributions from most simple transfer reactions. The 14С + 18О potential parameters were deduced. Isotopic differenc-es of the 12, 13, 14С + 18О and 14С + 16, 18О potentials were investigated.

Isotopic effects in elastic and inelastic 12,13C + 16,18O scattering

Directory of Open Access Journals (Sweden)

A. T. Rudchik

2010-09-01

Full Text Available New angular-distribution data of 13С + 18О elastic and inelastic scattering at the energy Elab(18O = 105 MeV were obtained for the transitions to the ground and excited states 3.088 MeV(1/2+, 3.555 MeV (1/2-, 3.854 MeV (5/2+ of 13С and 1.982 MeV (2+, 3.555 MeV (4+, 3.921 MeV (2+, 4.456 MeV (1-, 5.098 MeV (3-, 5.260 MeV (2+ of 18O. These and the 13С + 18О elastic scattering data taken from the literature at the energies Elab(18O = 15, 20, 24, 31 MeV and Elab(13С = 24 MeV were analysed within the optical model and coupled-reaction-channels methods. Sets of 13С + 18О optical potential parameters and their energy dependence were obtained. Contributions of potential scattering and transfer reactions to the elastic and inelastic channels of 13С + 18О scattering were studied. Isotopic differences (effects in 12, 13С + 16, 18О optical potential parameters were investigated.

Synthesis and hydration behavior of calcium zirconium aluminate (Ca7ZrAl6O18) cement

International Nuclear Information System (INIS)

Kang, Eun-Hee; Yoo, Jun-Sang; Kim, Bo-Hye; Choi, Sung-Woo; Hong, Seong-Hyeon

2014-01-01

Calcium zirconium aluminate (Ca 7 ZrAl 6 O 18 ) cements were prepared by solid state reaction and polymeric precursor methods, and their phase evolution, morphology, and hydration behavior were investigated. In polymeric precursor method, a nearly single phase Ca 7 ZrAl 6 O 18 was obtained at relatively lower temperature (1200 °C) whereas in solid state reaction, a small amount of CaZrO 3 coexisted with Ca 7 ZrAl 6 O 18 even at higher temperature (1400 °C). Unexpectedly, Ca 7 ZrAl 6 O 18 synthesized by polymeric precursor process was the large-sized and rough-shaped powder. The planetary ball milling was employed to control the particle size and shape. The hydration behavior of Ca 7 ZrAl 6 O 18 was similar to that of Ca 3 Al 2 O 6 (C3A), but the hydration products were Ca 3 Al 2 O 6 ·6H 2 O (C3AH6) and several intermediate products. Thus, Zr (or ZrO 2 ) stabilized the intermediate hydration products of C3A

Multi-isotopic composition (δ7Li-δ11B-δD-δ18O) of rainwaters in France: Origin and spatio-temporal characterization

International Nuclear Information System (INIS)

Millot, Romain; Petelet-Giraud, Emmanuelle; Guerrot, Catherine; Negrel, Philippe

2010-01-01

Research highlights: → A contour map of France for δ 18 O was drawn after compiling data that included more than 400 values from all of France. → The seasonal effect (i.e. the month or rainfall amount) is not the main controlling factor for the Li and B isotopic variations. → Most Li and B in rainwaters does not have a marine origin. → Finally, this work also adds to the potential for use of Li and B isotopes as environmental tracers. - Abstract: In the present work, the first results are reported for both Li and B isotope ratios in rainwater samples collected over a long time period (i.e. monthly rainfall events over 1 a) at a national scale (from coastal and inland locations). In addition, the stable isotopes of the water molecule (δD and δ 18 O) are also reported here for the same locations so that the Li and B isotope data can be discussed in the same context. The range of Li and B isotopic variations in these rainwaters were measured to enable the determination of the origin of these elements in rainwaters and the characterization of both the seasonal and spatio-temporal effects for δ 7 Li and δ 11 B signatures in rainwaters. Lithium and B concentrations are low in rainwater samples, ranging from 0.004 to 0.292 μmol/L and from 0.029 to 6.184 μmol/L, respectively. δ 7 Li and δ 11 B values in rainwaters also show a great range of variation between +3.2 per mille and +95.6 per mille and between -3.3 per mille and +40.6 per mille over a period of 1 a, respectively, clearly different from the signature of seawater. Seasonal effects (i.e. rainfall amount and month) are not the main factors controlling element concentrations and isotopic variations. δ 7 Li and δ 11 B values in rainwaters are clearly different from one site to another, indicating the variable contribution of sea salts in the rainwater depending on the sampling site (coastal vs. inland: also called the distance-from-the-coast-effect). This is well illustrated when wind direction data

Contribution of nuclear microanalysis and of 18O tracer technique to study the oxygen sublattice in high Tc superconducting thin films

International Nuclear Information System (INIS)

Siejka, J.

1994-01-01

At first a short review of IBA contribution to the determination of composition and structure, including phonon properties of high T c superconducting oxides is presented. In the second part, IBA contribution to the elucidation of the mechanisms of thin film growth is presented. The emphasis is on the complementarity of IBA, Raman spectroscopy and XRD techniques to characterize thin films of high T c superconducting oxides. In the third part, some recent results related mainly to YBaCuO films grown on (100) oriented single crystalline bulk materials (MgO, LaAlO 3 , SrTiO 3 ) is discussed. In these experiments, IBA, XRD and Raman spectroscopies were used to study the oxygen content in a series of YBaCuO films prepared in different conditions of pressure and temperature. In the case of c-axis oriented films a good agreement between these three methods was found for the films cooled down at high oxygen pressure and a significant disagreement for the films cooled down at low oxygen pressure, showing structures with anomalous c-axis parameter. In the case of a-axis oriented films grown on SrTiO 3 substrates it was found that the low T c values (∼ 70-80 K) are not correlated with the oxygen content but rather with a disorder in the oxygen sublattice. The disorder in the oxygen sublattice was studied using the 16 O(α, α) 16 O resonance in random and channeling geometry. These results are correlated with the data provided by Raman spectroscopy. The 18 O tracer technique was used to estimate the diffusion coefficient in the a-axis oriented YBaCuO films showing a huge anisotropy of the 18 O labelling. Combining Raman and IBA techniques, the selective 18 O labelling of the CuO chain-planes was evidenced. The defects in the 18 O enriched CuO chain-planes were studied using the 18 O(p, α) 15 N nuclear resonant reaction in random and channeling geometries. Some preliminary results related to roughness of YBaCuO films are also discussed. The physical implications of these

Organochlorine contaminant and stable isotope profiles in Arctic fox (Alopex lagopus) from the Alaskan and Canadian Arctic

Energy Technology Data Exchange (ETDEWEB)

Hoekstra, P.F.; Braune, B.M.; O' Hara, T.M.; Elkin, B.; Solomon, K.R.; Muir, D.C.G

2003-04-01

PCBs in Arctic fox are lower than reported in other Arctic populations and unlikely to cause significant impairment of reproductive success. - Arctic fox (Alopex lagopus) is a circumpolar species distributed across northern Canada and Alaska. Arctic fox muscle and liver were collected at Barrow, AK, USA (n=18), Holman, NT, Canada (n=20), and Arviat, NU, Canada (n=20) to elucidate the feeding ecology of this species and relate these findings to body residue patterns of organochlorine contaminants (OCs). Stable carbon ({delta}{sup 13}C) and nitrogen ({delta}{sup 15}N) isotope analyses of Arctic fox muscle indicated that trophic position (estimated by {delta}{sup 15}N) is positively correlated with increasing {delta}{sup 13}C values, suggesting that Arctic fox with a predominately marine-based foraging strategy occupy a higher trophic level than individuals mostly feeding from a terrestrial-based carbon source. At all sites, the rank order for OC groups in muscle was polychlorinated biphenyls ({sigma}PCB) > chlordane-related compounds ({sigma}CHLOR) > hexachlorocyclohexane ({sigma}HCH) > total toxaphene (TOX) {>=}chlorobenzenes ({sigma}ClBz) > DDT-related isomers ({sigma}DDT). In liver, {sigma}CHLOR was the most abundant OC group, followed by {sigma}PCB > TOX > {sigma}HCH > {sigma}ClBz > {sigma}DDT. The most abundant OC analytes detected from Arctic fox muscle and liver were oxychlordane, PCB-153, and PCB-180. The comparison of {delta}{sup 15}N with OC concentrations indicated that relative trophic position might not accurately predict OC bioaccumulation in Arctic fox. The bioaccumulation pattern of OCs in the Arctic fox is similar to the polar bear. While {sigma}PCB concentrations were highly variable, concentrations in the Arctic fox were generally below those associated with the toxicological endpoints for adverse effects on mammalian reproduction. Further research is required to properly elucidate the potential health impacts to this species from exposure to OCs.

Spatial distribution of bottlenose dolphins (Tursiops truncatus) inferred from stable isotopes and priority organic pollutants

Energy Technology Data Exchange (ETDEWEB)

Wilson, Rachel Marie, E-mail: ryounge@ocean.fsu.edu [Department of EOAS-Oceanography, Florida State University, 117 North Woodward Avenue, Tallahassee, Florida, 32306 (United States); Kucklick, John R. [National Institute of Standards and Technology, Hollings Marine Laboratory, Charleston, 331 Fort Johnson Road, Charleston, South Carolina 29412 (United States); Balmer, Brian C.; Wells, Randall S. [Chicago Zoological Society c/o Mote Marine Laboratory, 1600 Ken Thompson Parkway Sarasota, FL, 34236 (United States); Chanton, Jeffrey P. [Department of EOAS-Oceanography, Florida State University, 117 North Woodward Avenue, Tallahassee, Florida, 32306 (United States); Nowacek, Douglas P. [Nicholas School of the Environment and Pratt School of Engineering, Duke University - Marine Laboratory, 135 Duke Marine Lab Rd., Beaufort, NC 28516 (United States)

2012-05-15

Differences in priority organic pollutants (POPs), analyzed by gas chromatography-mass spectrometry, and stable isotope ratios ({delta}{sup 13}C, {delta}{sup 34}S, and {delta}{sup 15}N; analyzed by isotope ratio-mass spectrometry), divide 77 bottlenose dolphins (Tursiops truncatus) from the Florida Gulf Coast into three distinct groups. POP levels reflect human population and historical contamination along the coast. In the least disturbed site, concentrations of {Sigma}POP in male dolphins were 18,000 ng g{sup -1} {+-} 6000 (95% confidence interval here and throughout); in the intermediate bay, males had {Sigma}POP concentrations of 19,000 ng g{sup -1} {+-} 10,000. St Andrews Bay was home to dolphins with the highest {Sigma}POP concentrations: 44,000 ng g{sup -1} {+-} 10,300. {delta}{sup 34}S and {delta}{sup 15}N, differed significantly between St. George Sound dolphins and those frequenting each of the other two bays, but not between St. Andrews and St. Joseph Bays. {Sigma}POP concentrations were statistically higher in dolphins frequenting St. Andrews Bay, but were not significantly different between dolphins occupying St. Joseph Bay and St. George Sound. Thus, using either POP or isotope values alone, we would only be able to identify two dolphin groups, but when POP and isotope data are viewed cumulatively, the results clearly define three distinct communities occupying this region. - Highlights: Black-Right-Pointing-Pointer We compare isotopes and POP levels in dolphins occupying three embayments. Black-Right-Pointing-Pointer POP levels varied significantly among two embayments separated by < 50 km. Black-Right-Pointing-Pointer Differentiation correlated with historical contamination from a SuperFund site. Black-Right-Pointing-Pointer Cumulatively, isotopes and POP levels indicate 3 distinct dolphin communities. Black-Right-Pointing-Pointer This data provides the first assessment of dolphin POP contamination in the region.

TDA's validity to study 18O collectivity in terms of collective pair model

International Nuclear Information System (INIS)

Gao Yuanyi; Vitturi, A.; Catara, F.; Sambataro, M.

1991-01-01

Conclusion proved that if the authors calculate 18 O collective spectra in terms of the Collective Pair Model, the authors can get the positive low laying levels of 18 O which are of the particle particle pair, independent on the excitation of hole within closed shell. 1 - low laying levels are of non-collective 3 particle 1 hole states. 1 - fourth level is of collective 3 particle 1 hole states. 3 - low laying levels are of collective 3 particle 1 hole states. 1 - , 3 - low laying levels agree very well with the experiment data. Hence the TDA is sufficient for the calculations of 1 - ,3 - collective low levels of 18 O

Espiritu Santo, Vanuatu Stable Isotope (delta 18O, delta 13C) Data for 1806 to 1979

Data.gov (United States)

National Oceanic and Atmospheric Administration, Department of Commerce — Site: Espiritu Santo Island, Vanuatu, 15S, 167E. 173 year record of d18O and d13C. Variable names: QSR Age, QSR 13C, QSR 18O, GRL Age, GRL Qtrly 13C, GRL Qtrly 18O,...

Stable isotope analyses of oxygen (18O:17O:16O) and chlorine (37Cl:35Cl) in perchlorate: reference materials, calibrations, methods, and interferences

Science.gov (United States)

Böhlke, John Karl; Mroczkowski, Stanley J.; Sturchio, Neil C.; Heraty, Linnea J.; Richman, Kent W.; Sullivan, Donald B.; Griffith, Kris N.; Gu, Baohua; Hatzinger, Paul B.

2017-01-01

RationalePerchlorate (ClO4−) is a common trace constituent of water, soils, and plants; it has both natural and synthetic sources and is subject to biodegradation. The stable isotope ratios of Cl and O provide three independent quantities for ClO4− source attribution and natural attenuation studies: δ37Cl, δ18O, and δ17O (or Δ17O or 17Δ) values. Documented reference materials, calibration schemes, methods, and interferences will improve the reliability of such studies.MethodsThree large batches of KClO4 with contrasting isotopic compositions were synthesized and analyzed against VSMOW-SLAP, atmospheric O2, and international nitrate and chloride reference materials. Three analytical methods were tested for O isotopes: conversion of ClO4− to CO for continuous-flow IRMS (CO-CFIRMS), decomposition to O2 for dual-inlet IRMS (O2-DIIRMS), and decomposition to O2 with molecular-sieve trap (O2-DIIRMS+T). For Cl isotopes, KCl produced by thermal decomposition of KClO4 was reprecipitated as AgCl and converted into CH3Cl for DIIRMS.ResultsKClO4 isotopic reference materials (USGS37, USGS38, USGS39) represent a wide range of Cl and O isotopic compositions, including non-mass-dependent O isotopic variation. Isotopic fractionation and exchange can affect O isotope analyses of ClO4− depending on the decomposition method. Routine analyses can be adjusted for such effects by normalization, using reference materials prepared and analyzed as samples. Analytical errors caused by SO42−, NO3−, ReO42−, and C-bearing contaminants include isotope mixing and fractionation effects on CO and O2, plus direct interference from CO2 in the mass spectrometer. The results highlight the importance of effective purification of ClO4− from environmental samples.ConclusionsKClO4 reference materials are available for testing methods and calibrating isotopic data for ClO4− and other substances with widely varying Cl or O isotopic compositions. Current ClO4−extraction, purification

Water and nitrogen conditions affect the relationships of Delta13C and Delta18O to gas exchange and growth in durum wheat.

Science.gov (United States)

Cabrera-Bosquet, Llorenç; Molero, Gemma; Nogués, Salvador; Araus, José Luis

2009-01-01

Whereas the effects of water and nitrogen (N) on plant Delta(13)C have been reported previously, these factors have scarcely been studied for Delta(18)O. Here the combined effect of different water and N regimes on Delta(13)C, Delta(18)O, gas exchange, water-use efficiency (WUE), and growth of four genotypes of durum wheat [Triticum turgidum L. ssp. durum (Desf.) Husn.] cultured in pots was studied. Water and N supply significantly increased plant growth. However, a reduction in water supply did not lead to a significant decrease in gas exchange parameters, and consequently Delta(13)C was only slightly modified by water input. Conversely, N fertilizer significantly decreased Delta(13)C. On the other hand, water supply decreased Delta(18)O values, whereas N did not affect this parameter. Delta(18)O variation was mainly determined by the amount of transpired water throughout plant growth (T(cum)), whereas Delta(13)C variation was explained in part by a combination of leaf N and stomatal conductance (g(s)). Even though the four genotypes showed significant differences in cumulative transpiration rates and biomass, this was not translated into significant differences in Delta(18)O(s). However, genotypic differences in Delta(13)C were observed. Moreover, approximately 80% of the variation in biomass across growing conditions and genotypes was explained by a combination of both isotopes, with Delta(18)O alone accounting for approximately 50%. This illustrates the usefulness of combining Delta(18)O and Delta(13)C in order to assess differences in plant growth and total transpiration, and also to provide a time-integrated record of the photosynthetic and evaporative performance of the plant during the course of crop growth.

Metrology for stable isotope reference materials: 13C/12C and 18O/16O isotope ratio value assignment of pure carbon dioxide gas samples on the Vienna PeeDee Belemnite-CO2 scale using dual-inlet mass spectrometry.

Science.gov (United States)

Srivastava, Abneesh; Michael Verkouteren, R

2018-05-25

Isotope ratio measurements have been conducted on a series of isotopically distinct pure CO 2 gas samples using the technique of dual-inlet isotope ratio mass spectrometry (DI-IRMS). The influence of instrumental parameters, data normalization schemes on the metrological traceability and uncertainty of the sample isotope composition have been characterized. Traceability to the Vienna PeeDee Belemnite(VPDB)-CO 2 scale was realized using the pure CO 2 isotope reference materials(IRMs) 8562, 8563, and 8564. The uncertainty analyses include contributions associated with the values of iRMs and the repeatability and reproducibility of our measurements. Our DI-IRMS measurement system is demonstrated to have high long-term stability, approaching a precision of 0.001 parts-per-thousand for the 45/44 and 46/44 ion signal ratios. The single- and two-point normalization bias for the iRMs were found to be within their published standard uncertainty values. The values of 13 C/ 12 C and 18 O/ 16 O isotope ratios are expressed relative to VPDB-CO 2 using the [Formula: see text] and [Formula: see text] notation, respectively, in parts-per-thousand (‰ or per mil). For the samples, value assignments between (-25 to +2) ‰ and (-33 to -1) ‰ with nominal combined standard uncertainties of (0.05, 0.3) ‰ for [Formula: see text] and [Formula: see text], respectively were obtained. These samples are used as laboratory reference to provide anchor points for value assignment of isotope ratios (with VPDB traceability) to pure CO 2 samples. Additionally, they serve as potential parent isotopic source material required for the development of gravimetric based iRMs of CO 2 in CO 2 -free dry air in high pressure gas cylinder packages at desired abundance levels and isotopic composition values. Graphical abstract CO 2 gas isotope ratio metrology.

Comprehensive inter-laboratory calibration of reference materials for δ18O versus VSMOW using various on-line high-temperature conversion techniques

Science.gov (United States)

Brand, Willi A.; Coplen, Tyler B.; Aerts-Bijma, Anita T.; Bohlke, John Karl; Gehre, Matthias; Geilmann, Heike; Groning, Manfred; Jansen, Henk G.; Meijer, Harro A. J.; Mroczkowski, Stanley J.; Qi, Haiping; Soergel, Karin; Stuart-Williams, Hilary; Weise, Stephan M.; Werner, Roland A.

2009-01-01

Internationally distributed organic and inorganic oxygen isotopic reference materials have been calibrated by six laboratories carrying out more than 5300 measurements using a variety of high-temperature conversion techniques (HTC) in an evaluation sponsored by the International Union of Pure and Applied Chemistry (IUPAC). To aid in the calibration of these reference materials, which span more than 125‰, an artificially enriched reference water (δ18O of +78.91‰) and two barium sulfates (one depleted and one enriched in 18O) were prepared and calibrated relative to VSMOW2 and SLAP reference waters. These materials were used to calibrate the other isotopic reference materials in this study, which yielded:Reference materialδ18O and estimated combined uncertainty IAEA-602 benzoic acid+71.28 ± 0.36‰USGS35 sodium nitrate+56.81 ± 0.31‰IAEA-NO-3 potassium nitrate+25.32 ± 0.29‰IAEA-601 benzoic acid+23.14 ± 0.19‰IAEA-SO-5 barium sulfate+12.13 ± 0.33‰NBS 127 barium sulfate+8.59 ± 0.26‰VSMOW2 water0‰IAEA-600 caffeine−3.48 ± 0.53‰IAEA-SO-6 barium sulfate−11.35 ± 0.31‰USGS34 potassium nitrate−27.78 ± 0.37‰SLAP water−55.5‰The seemingly large estimated combined uncertainties arise from differences in instrumentation and methodology and difficulty in accounting for all measurement bias. They are composed of the 3-fold standard errors directly calculated from the measurements and provision for systematic errors discussed in this paper. A primary conclusion of this study is that nitrate samples analyzed for δ18O should be analyzed with internationally distributed isotopic nitrates, and likewise for sulfates and organics. Authors reporting relative differences of oxygen-isotope ratios (δ18O) of nitrates, sulfates, or organic material should explicitly state in their reports the δ18O values of two or more internationally distributed nitrates (USGS34, IAEA-NO-3, and USGS35), sulfates (IAEA-SO-5, IAEA

Implications of the 14C(α,γ)18O reaction for nonstandard big bang nucleosynthesis

International Nuclear Information System (INIS)

Gai, M.

1992-01-01

The thermonuclear burning rates for the 14 C(α,γ) 18 O radiative capture reaction are calculated at temperatures (0.3 - state, at approximately 9.0 MeV in 18 O as would be deduced from the Yale-Michigan State University measurement of the beta-delayed alpha-particle emission of 18 N and suggested by the Notre Dame-Caltech measurement of the nonresonant 14 C(α,γ) 18 O cross section. The gamma widths of the proposed broad state is estimated using the Alhassid, Gai, and Bertsch sum rule, and an experimental study is proposed

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

Energy Technology Data Exchange (ETDEWEB)

Hendriksson, N. [Geological Survey of Finland, Espoo (Finland); Karhu, J.; Niinikoski, P. [Univ. of Helsinki (Finland)

2014-12-15

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{sup 18}O, - 82.3 per mille and -80.3 per mille for δ{sup 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{sup 2}H = 7.45 star δ{sup 18}O + 3.82. The isotope time series reveal a change in time. The increasing trend for the δ{sup 18}O and δ{sup 2}H values may be related to climatic variability while the gradual decline observed in the {sup 3}H data is attributed to the still continuing decrease in atmospheric {sup 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

Predictive value of brain 18F-FDG PET/CT in macrophagic myofasciitis?

OpenAIRE

Van Der Gucht, Axel; Abulizi, Mukedaisi; Blanc-Durand, Paul; Aoun-Sebaiti, Mehdi; Emsen, Berivan; Gherardi, Romain K.; Verger, Antoine; Authier, François-Jérôme; Itti, Emmanuel

2017-01-01

Abstract Rationale: Although several functional studies have demonstrated that positron emission tomography/computed tomography with 18F-fluorodeoxyglucose (18F-FDG PET/CT) appears to be efficient to identify a cerebral substrate in patients with known macrophagic myofasciitis (MMF), the predictive value of this imaging technique for MMF remains unclear. Patient concerns: We presented data and images of a 46-year-old woman. Diagnoses: The patient was referred to our center for suspected MMF d...

Investigation of the phase formation and dielectric properties of Bi7Ta3O18

International Nuclear Information System (INIS)

Chon, M.P.; Tan, K.B.; Khaw, C.C.; Zainal, Z.; Taufiq Yap, Y.H.; Chen, S.K.; Tan, P.Y.

2014-01-01

Highlights: • Synthesis condition of Bi 7 TaO 3 O 18 had been determined. • Recombination of intermediate BiTaO 4 and Bi 3 TaO 7 phases are required for the Bi 7 TaO 3 O 18 phase formation. • Stable material as confirmed by thermal and structural analyses. • Typical ferroelectric showing high dielectric constants and low losses. • Resonance and thermal activated polarisation processes are responsible for the excellent dielectric characteristic. -- Abstract: Polycrystalline Bi 7 Ta 3 O 18 was synthesised at the firing temperature of 950 °C over 18 h via conventional solid state method. It crystallised in a monoclinic system with space group C2/m, Z = 4 similar to that reported diffraction pattern in the Inorganic Crystal Structure Database (ICSD), 1-89-6647. The refined lattice parameters were a = 34.060 (3) Å, b = 7.618 (9) Å, c = 6.647 (6) Å with α = γ = 90° and β = 109.210 (7), respectively. The intermediate phase was predominantly in high-symmetry cubic structure below 800 °C and finally evolved into a low-symmetry monoclinic structured, Bi 7 Ta 3 O 18 at 950 °C. The sample contained grains of various shapes with different orientations in the size ranging from 0.33–22.70 μm. The elemental analysis showed the sample had correct stoichiometry with negligible Bi 2 O 3 loss. Bi 7 Ta 3 O 18 was thermally stable and it exhibited a relatively high relative permittivity, 241 and low dielectric loss, 0.004 at room temperature, ∼30 °C and frequency of 1 MHz

Model experiments for {sup 14}C water-age determinations

Energy Technology Data Exchange (ETDEWEB)

Wendt, I; Stahl, W; Geyh, M; Fauth, F [Bundesanstalt fuer Bodenforschung, Hannover (Germany)

1967-05-15

The {sup 14}C age of water samples is calculated by assuming that fossil carbonate is dissolved by biogenic CO{sub 2} according to the equation x{sub 1} {center_dot} CaCO{sub 3} + (x{sub 1}+y{sub 1}) {center_dot} CO{sub 2} + H{sub 2}O = 2x{sub 1} {center_dot} HCO{sub 3} + y{sub 1} {center_dot} CO{sub 2} where x and y are the number of moles of the two carbon components before and after the dissolution process. In a closed system the relation y{sub 1} = K(T) (x{sub 1}){sup 3} must be satisfied additionally. The equilibrium constant K(T), which depends on the temperature, controls the concentrations of free CO{sub 2} and HCO{sub 3}. To investigate the mechanism of the dissolution, laboratory experiments under controlled conditions were carried out. Non-radioactive CaCO{sub 3}, which had a {delta}{sup 13}C-value of +30 per mille, and radioactive CO{sub 2} with {delta}{sup 13}C = -22 per mille were used. The purpose of these investigations was to check the validity of theoretical assumptions regarding the average {sup 14}C-activity and the {delta}{sup 13}C-value of the total carbon which is dissolved as CO{sub 2} and HCO{sub 3}. Furthermore, it was investigated whether, within the duration of the experiment, a possible exchange takes place between the undissolved carbon present in the CaCO{sub 3} and that present in the HCO{sub 3}. The importance of this lies in the fact that the method of {sup 14}C age determination is based on the assumption that such an exchange does not take place. The experiments which have been performed up to now show that in case of the simple CaCO{sub 3} - CO{sub 2} system, which has been considered first, this assumption is not justified even for a constant water temperature. If variations in the water temperature occur during the history of the water sample, precipitation and redissolution processes influence the {sup 14}C- and {delta}{sup 13}C -values differently. This is due to isotopic fractionation processes between the HCO{sub 3} and CO

W18O49 nanowires assembled on carbon felt for application to supercapacitors

Science.gov (United States)

Jung, Jinjoo; Kim, Do Hyung

2018-03-01

For supercapacitor applications, W18O49 nanowires have been extensively grown on graphitic carbon felt using a facile solvothermal method. The diameter and length of the nanowires are about 7 and 300 nm, respectively. The nanowires consist of monoclinic W18O49 grown along the [010] direction, as shown by TEM and XRD analyses. The W18O49 nanowires, assembled on carbon felt, exhibit a high capacity of 588.33 F/g at a current density of 1 A/g together with an excellent cycle performance, and a low internal resistance during the electrochemical tests. This outstanding performance may originate from the three-dimensional porous nanostructure of these W18O49 nanowires, which leads to a reduction in the resistance and fast reaction kinetics due to the high specific surface area and electrolyte accessibility. Furthermore, sufficient oxygen deficiencies of the substoichiometric tungsten oxide can also contribute to the electrochemical activity, which can be confirmed by comparison of CV and EIS data with WO3 nanowires.

Synthesis and applications of 18O standards for nuclear reaction analysis

Science.gov (United States)

Pitthan, E.; Corrêa, S. A.; Soares, G. V.; Radtke, C.; Stedile, F. C.

2014-08-01

A new method to synthesize 18O standard samples to be used in nuclear reaction analyses is proposed and investigated. This method consists of obtaining a Si18O2 film on a Si substrate using a natural abundance SiO2 film as a passivation layer to prevent the isotopically enriched film to be exposed to the atmosphere and possibly degraded by it. For that, sequential oxidation steps are performed followed by a controlled etching in aqueous hydrofluoric acid. Details of these steps are discussed as well as the stability of the synthesized samples. Applications using these standard samples in the field of alternative semiconductors to Si (SiC and Ge), used in micro and nanoelectronics are also presented.

Impact of convective activity on precipitation δ18O in isotope-enabled models

Science.gov (United States)

Hu, J.; Emile-Geay, J.; Dee, S.

2017-12-01

The ^18O signal preserved in paleo-archives (e.g. speleothem, tree ring cellulose, ice cores) is widely used to reconstruct precipitation or temperature. In the tropics, the inverse relationship between precipitation ^18O and rainfall amount, namely "amount effect" [Dansgaard, Tellus, 1964], is often used to interpret precipitation ^18O. However, recent studies have shown that precipitation ^18O is also influenced by precipitation type [Kurita et al, JGR, 2009; Moerman et al, EPSL, 2013], and recent observations indicate that it is negatively correlated with the fraction of precipitation associated with stratiform clouds [Aggarwal et al, Nature Geosci, 2016]. It is thus important to determine to what extent isotope-enabled climate models can reproduce these relationships. Here we do so using output from LMDZ, CAM2, and isoGSM from the Stable Water Isotope Intercomparison Group, Phase 2 (SWING2) project and results of SPEEDY-IER [Dee et al, JGR, 2015] from an AMIP-style experiment. The results show that these models simulate the "amount effect" well in the tropics, and the relationship between precipitation ^18O and precipitation is reversed in many places in mid-latitudes, in accordance with observations [Bowen, JGR, 2008]. Also, these models can all reproduce the negative correlation between monthly precipitation ^18O and stratiform precipitation proportion in mid-latitude (30°N-50°N; 50°S-30°S), but in the tropics (30°S-30°N), models show a positive correlation instead. The reason for this bias will be investigated within idealized experiments with SPEEDY-IER. The correct simulations of the impact of convective activity on precipitation ^18O in isotope-enabled models will improve our interpretation of paleoclimate proxies with respect to hydroclimate variability. P. K. Aggarwal et al. (2016), Nature Geosci., 9, 624-629, doi:10.1038/ngeo2739. G. J. Bowen. (2008), J. Geophys. Res., 113, D05113, doi:10.1029/2007JD009295. W. Dansgaard (1964), Tellus, 16(4), 436

Evidence for a universal pathway of abscisic acid biosynthesis in higher plants from sup 18 O incorporation patterns

Energy Technology Data Exchange (ETDEWEB)

Zeevaart, J.A.D.; Heath, T.G.; Gage, D.A. (Michigan State University, East Lansing (USA))

1989-12-01

Previous labeling studies of abscisic acid (ABA) with {sup 18}O{sub 2} have been mainly conducted with water-stressed leaves. In this study, {sup 18}O incorporation into ABA of stressed leaves of various species was compared with {sup 18}O labeling of ABA of turgid leaves and of fruit tissue in different stages of ripening. In stressed leaves of all six species investigated, avocado (Persea americana), barley (Hordeum vulgare), bean (Phaseolus vulgaris), cocklebur (Xanthium strumarium), spinach (Spinacia oleracea), and tobacco (Nicotiana tabacum), {sup 18}O was most abundant in the carboxyl group, whereas incorporation of a second and third {sup 18}O in the oxygen atoms on the ring of ABA was much less prominent after 24 h in {sup 18}O{sub 2}. ABA from turgid bean leaves showed significant {sup 18}O incorporation, again with highest {sup 18}O enrichment in the carboxyl group. On the basis of {sup 18}O-labeling patterns observed in ABA from different tissues it is concluded that, despite variations in precusor pool sizes and intermediate turnover rates, there is a universal pathway of ABA biosynthesis in higher plants which involves cleavage of a larger precursor molecule, presumably an oxygenated carotenoid.

Can tree-ring isotopes (δ18O and δ13C) improve our understanding of hydroclimate variability in the Columbia River Basin?

Science.gov (United States)

Csank, A. Z.; Wise, E.; McAfee, S. A.

2015-12-01

The trajectory of incoming storms from the Pacific Ocean has a strong impact on hydroclimate in the Pacific Northwest. Shifts between zonal and meridional flow are a key influence on drought and pluvial regimes in both the PNW and the western United States as a whole. Circulation-dependent variability in the isotopic composition of precipitation can be recorded and potentially reconstructed using δ18O records derived from tree-rings. Here we present isotopic records of δ18O and δ13C from ponderosa pine (Pinus ponderosa) for the period 1950-2013 from six sites located in the lee of the Cascades in eastern Washington. Because of the orientation of the Cascades, zonal flow will result in an intensified rain shadow whereas meridional flow allows moisture to penetrate at a lower elevation leading to a lower rainout effect. This means zonal flow results in drier conditions in eastern Washington and the converse for meridional flow. We hypothesized that more depleted precipitation δ18O values will occur with periods of more zonal flow across the PNW and will be recorded by trees at our sites. Results show a strong relationship between our δ18O chronologies and winter precipitation (R = -0.50; p<0.001). δ13C chronologies from the same trees showed a relationship to prior fall/winter (pOct-pDec) precipitation (R = -0.46; p<0.005) suggesting a possible link to antecedent moisture conditions. With a focus on years with clear zonal and meridional flow regimes, we regressed the tree-ring δ18O anomaly against the instrumental record of total precipitation and compared the residual series to records of storm track for the period 1978-2008, and we found a detectable signal where the most depleted δ18O was generally associated with zonal flow and the most enriched δ18O with meridional flow. However, there are still some years where the relationship is unclear. Further work is aimed at understanding these anomalous years and extending our record beyond the instrumental