Assessment of groundwater salinization mechanisms in Santiago Island - Cabo Verde: An environmental isotopic approach

International Nuclear Information System (INIS)

Carreira, P.M.; Nunes, D.; Marques, J.M.; Pina, A.; Mota Gomes, A.; Almeida, E.; Goncalves, R.; Monteiro Santos, F.

2007-01-01

Two sampling campaigns were carried out at Santiago Island - Cabo Verde under the scope of an isotopic and geochemical research study. An evaluation of the groundwater systems was carried out through the application of environmental isotopes and geochemical data in order to answer questions such as: origin and mechanisms of groundwater recharge; relation between the hydrochemical evolution of the groundwater systems with the geological matrix (minerals dissolution) or mixture with seawater and aerosol marine influence; identification of seawater intrusion mechanisms and, determination of the apparent groundwater 'age'. The results obtained so far are not conclusive on the identification of the process responsible for the increase of salinity. In general, all the data obtained seems to indicate that the waters have the same isotopic history but different geochemical evolution, which depends on the weathering and permeability of the rocks. (author)

Multi-saline sample distillation apparatus for hydrogen isotope analyses: design and accuracy. Water-resources investigations

International Nuclear Information System (INIS)

Hassan, A.A.

1981-04-01

A distillation apparatus for saline water samples was designed and tested. Six samples may be distilled simultaneously. The temperature was maintained at 400 degrees C to ensure complete dehydration of the precipitating salts. Consequently, the error in the measured ratio of stable hydrogen isotopes resulting from incomplete dehydration of hydrated salts during distillation was eliminated

Faunal and oxygen isotopic evidence for surface water salinity changes during sapropel formation in the eastern Mediterranean

International Nuclear Information System (INIS)

Williams, D.F.; Thunell, R.C.

1979-01-01

The discovery of the widespread anaerobic deposits (sapropels) in late Cenozoic sediments of the eastern Mediteranean has prompted many workers to propose the periodic occurrence of extremely low surface salinites in the Mediterranean. Oxygen isotopic determinations and total faunal analyses were made at 1000-year intervals across two equivalent sapropels in two piston cores from the Levantine Basin. The sapropel layers were deposited approximately 9000 y.B.P. (Sapropel A) and 80, 000 y. B.P. (Sapropel B). Significant isotopic anomalies were recorded by the foraminiferal species within Sapropels A and B in both cores. The surface dwelling species record a larger 18 O depletion than the mesopelagic species suggesting that surface salinities were reduced by 2-3per 1000 during sapropel formation. The faunal changes associated with the sapropels also indicate that the oceanographic conditions which lead to anoxic conditions in the eastern Mediteranean involve the formation of a low salinity surface layer. The source of the low salinity water might be meltwater produced by disintegration of the Fennoscandian Ice Sheet which drained into the Black Sea, into the Aegean Sea and finally into the eastern Mediterranean. (Auth.)

Cl/Br ratios and chlorine isotope evidences for groundwater salinization and its impact on groundwater arsenic, fluoride and iodine enrichment in the Datong basin, China

Energy Technology Data Exchange (ETDEWEB)

Li, Junxia; Wang, Yanxin, E-mail: yx.wang@cug.edu.cn; Xie, Xianjun

2016-02-15

In order to identify the salinization processes and its impact on arsenic, fluoride and iodine enrichment in groundwater, hydrogeochemical and environmental isotope studies have been conducted on groundwater from the Datong basin, China. The total dissolved solid (TDS) concentrations in groundwater ranged from 451 to 8250 mg/L, and 41% of all samples were identified as moderately saline groundwater with TDS of 3000–10,000 mg/L. The results of groundwater Cl concentrations, Cl/Br molar ratio and Cl isotope composition suggest that three processes including water-rock interaction, surface saline soil flushing, and evapotranspiration result in the groundwater salinization in the study area. The relatively higher Cl/Br molar ratio in groundwater from multiple screening wells indicates the contribution of halite dissolution from saline soil flushed by vertical infiltration to the groundwater salinization. However, the results of groundwater Cl/Br molar ratio model indicate that the effect of saline soil flushing practice is limited to account for the observed salinity variation in groundwater. The plots of groundwater Cl vs. Cl/Br molar ratio, and Cl vs δ{sup 37}Cl perform the dominant effects of evapotranspiration on groundwater salinization. Inverse geochemical modeling results show that evapotranspiration may cause approximately 66% loss of shallow groundwater to account for the observed hydrochemical pattern. Due to the redox condition fluctuation induced by irrigation activities and evapotranspiration, groundwater salinization processes have negative effects on groundwater arsenic enrichment. For groundwater iodine and fluoride enrichment, evapotranspiration partly accounts for their elevation in slightly saline water. However, too strong evapotranspiration would restrict groundwater fluoride concentration due to the limitation of fluorite solubility. - Highlights: • Natural high arsenic, fluoride and iodine groundwater co-occur with saline water. �

Cl/Br ratios and chlorine isotope evidences for groundwater salinization and its impact on groundwater arsenic, fluoride and iodine enrichment in the Datong basin, China

International Nuclear Information System (INIS)

Li, Junxia; Wang, Yanxin; Xie, Xianjun

2016-01-01

In order to identify the salinization processes and its impact on arsenic, fluoride and iodine enrichment in groundwater, hydrogeochemical and environmental isotope studies have been conducted on groundwater from the Datong basin, China. The total dissolved solid (TDS) concentrations in groundwater ranged from 451 to 8250 mg/L, and 41% of all samples were identified as moderately saline groundwater with TDS of 3000–10,000 mg/L. The results of groundwater Cl concentrations, Cl/Br molar ratio and Cl isotope composition suggest that three processes including water-rock interaction, surface saline soil flushing, and evapotranspiration result in the groundwater salinization in the study area. The relatively higher Cl/Br molar ratio in groundwater from multiple screening wells indicates the contribution of halite dissolution from saline soil flushed by vertical infiltration to the groundwater salinization. However, the results of groundwater Cl/Br molar ratio model indicate that the effect of saline soil flushing practice is limited to account for the observed salinity variation in groundwater. The plots of groundwater Cl vs. Cl/Br molar ratio, and Cl vs δ"3"7Cl perform the dominant effects of evapotranspiration on groundwater salinization. Inverse geochemical modeling results show that evapotranspiration may cause approximately 66% loss of shallow groundwater to account for the observed hydrochemical pattern. Due to the redox condition fluctuation induced by irrigation activities and evapotranspiration, groundwater salinization processes have negative effects on groundwater arsenic enrichment. For groundwater iodine and fluoride enrichment, evapotranspiration partly accounts for their elevation in slightly saline water. However, too strong evapotranspiration would restrict groundwater fluoride concentration due to the limitation of fluorite solubility. - Highlights: • Natural high arsenic, fluoride and iodine groundwater co-occur with saline water. • Groundwater

The density-salinity relation of standard seawater

Science.gov (United States)

Schmidt, Hannes; Seitz, Steffen; Hassel, Egon; Wolf, Henning

2018-01-01

The determination of salinity by means of electrical conductivity relies on stable salt proportions in the North Atlantic Ocean, because standard seawater, which is required for salinometer calibration, is produced from water of the North Atlantic. To verify the long-term stability of the standard seawater composition, it was proposed to perform measurements of the standard seawater density. Since the density is sensitive to all salt components, a density measurement can detect any change in the composition. A conversion of the density values to salinity can be performed by means of a density-salinity relation. To use such a relation with a target uncertainty in salinity comparable to that in salinity obtained from conductivity measurements, a density measurement with an uncertainty of 2 g m-3 is mandatory. We present a new density-salinity relation based on such accurate density measurements. The substitution measurement method used is described and density corrections for uniform isotopic and chemical compositions are reported. The comparison of densities calculated using the new relation with those calculated using the present reference equations of state TEOS-10 suggests that the density accuracy of TEOS-10 (as well as that of EOS-80) has been overestimated, as the accuracy of some of its underlying density measurements had been overestimated. The new density-salinity relation may be used to verify the stable composition of standard seawater by means of routine density measurements.

Quantum mechanical calculation of diffusion of hydrogen isotopes in vanadium

International Nuclear Information System (INIS)

Yoshinari, Osamu

2013-01-01

Highlights: • Diffusion of H isotopes in V was investigated with a quantum mechanical calculation. • Calculated diffusion coefficients quantitatively agreed with the experimental data. • H in V jumps via quantum mechanical tunneling between the two tetrahedral sites. • H tunneling between ground states is dominant at low temperatures. • H tunneling between exited states becomes important at higher temperatures. -- Abstract: Diffusion of hydrogen isotopes in vanadium was investigated by a quantum mechanical calculation. Wave functions and the corresponding eigen energies (E) for hydrogen isotopes were obtained as a function of hydrogen position along the diffusion path (ξ) by solving the three dimensional Schrödinger equation. Hydrogen potential was calculated by using a first principles method with a nudged elastic band technique. By analyzing the E–ξ curves, the tunneling matrix elements were obtained for the coincidence states between two neighboring tetrahedral sites. It was clarified that the tunneling between ground states was dominant at low temperatures, whereas the contribution of that between the first exited states becomes larger at higher temperatures. The transition temperature of the dominant tunneling decreases with the isotope mass. The calculated temperature dependence of the diffusion for the V–H system quantitatively agreed with the experimental data in the literature, although those for the V–D and –T systems were somewhat underestimated

Origin of salinity in produced waters from the Palm Valley gas field, Northern Territory, Australia

International Nuclear Information System (INIS)

Andrew, Anita S.; Whitford, David J.; Berry, Martin D.; Barclay, Stuart A.; Giblin, Angela M.

2005-01-01

The chemical composition and evolution of produced waters associated with gas production in the Palm Valley gas field, Northern Territory, has important implications for issues such as gas reserve calculations, reservoir management and saline water disposal. The occurrence of saline formation water in the Palm Valley field has been the subject of considerable debate. There were no occurrences of mobile water early in the development of the field and only after gas production had reduced the reservoir pressure, was saline formation water produced. Initially this was in small quantities but has increased dramatically with time, particularly after the initiation of compression in November 1996. The produced waters range from highly saline (up to 300,000 mg/L TDS), with unusual enrichments in Ca, Ba and Sr, to low salinity fluids that may represent condensate waters. The Sr isotopic compositions of the waters ( 87 Sr/ 86 Sr = 0.7041-0.7172) are also variable but do not correlate closely with major and trace element abundances. Although the extreme salinity suggests possible involvement of evaporite deposits lower in the stratigraphic sequence, the Sr isotopic composition of the high salinity waters suggests a more complex evolutionary history. The formation waters are chemically and isotopically heterogeneous and are not well mixed. The high salinity brines have Sr isotopic compositions and other geochemical characteristics more consistent with long-term residence within the reservoir rocks than with present-day derivation from a more distal pool of brines associated with evaporites. If the high salinity brines entered the reservoir during the Devonian uplift and were displaced by the reservoir gas into a stagnant pool, which has remained near the reservoir for the last 300-400 Ma, then the size of the brine pool is limited. At a minimum, it might be equivalent to the volume displaced by the reservoired gas

Calculation of isotopic profile during band displacement on ion exchange resins

International Nuclear Information System (INIS)

Sonwalkar, A.S.; Puranik, V.D.; D'Souza, A.B.

1981-01-01

A method has been developed to calculate the isotopic profile during band displacement on ion exchange resins using computer simulation. Persoz had utilized this technique earlier for calculating the isotopic profile during band displacement as well as frontal analysis. The present report deals with a simplification of the method used by Persoz by reducing the number of variables and making certain approximations where the separation factor is not far from unity. Calculations were made for the typical case of boron isotope separation. The results obtained by the modified method were found to be in very good agreement with those obtained by using an exact equation, at the same time requiring conside--rably less computer time. (author)

Tackling the salinity-pollution nexus in coastal aquifers from arid regions using nitrate and boron isotopes.

Science.gov (United States)

Re, V; Sacchi, E

2017-05-01

Salinization and nitrate pollution are generally ascertained as the main issues affecting coastal aquifers worldwide. In arid zones, where agricultural activities also result in soil salinization, both phenomena tend to co-exist and synergically contribute to alter groundwater quality, with severe negative impacts on human populations and natural ecosystems' wellbeing. It becomes therefore necessary to understand if and to what extent integrated hydrogeochemical tools can help in distinguishing among possible different salinization and nitrate contamination origins, in order to provide adequate science-based support to local development and environmental protection. The alluvial plain of Bou-Areg (North Morocco) extends over about 190 km 2 and is separated from the Mediterranean Sea by the coastal Lagoon of Nador. Its surface is covered for more than 60% by agricultural activities, although the region has been recently concerned by urban population increase and tourism expansion. All these activities mainly rely on groundwater exploitation and at the same time are the main causes of both aquifer and lagoon water quality degradation. For this reason, it was chosen as a case study representative of the typical situation of coastal aquifers in arid zones worldwide, where a clear identification of salinization and pollution sources is fundamental for the implementation of locally oriented remedies and long-term management strategies. Results of a hydrogeochemical investigation performed between 2009 and 2011 show that the Bou-Areg aquifer presents high salinity (often exceeding 100 mg/L in TDS) due to both natural and anthropogenic processes. The area is also impacted by nitrate contamination, with concentrations generally exceeding the WHO statutory limits for drinking water (50 mg/L) and reaching up to about 300 mg/L, in both the rural and urban/peri-urban areas. The isotopic composition of dissolved nitrates (δ 15 N NO3 and δ 18 O NO ) was used to constrain

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

International Nuclear Information System (INIS)

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

2015-01-01

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

Geochemical and isotopic determination of deep groundwater contributions and salinity to the shallow groundwater and surface water systems, Mesilla Basin, New Mexico, Texas, and Mexico

Science.gov (United States)

Robertson, A.; Carroll, K. C.; Kubicki, C.; Purtshert, R.

2017-12-01

The Mesilla Basin/Conejos-Médanos aquifer system, extending from southern New Mexico to Chihuahua, Mexico, is a priority transboundary aquifer under the 2006 United States­-Mexico Transboundary Aquifer Assessment Act. Declining water levels, deteriorating water quality, and increasing groundwater use by municipal, industrial, and agricultural users on both sides of the international border raise concerns about long-term aquifer sustainability. Relative contributions of present-day and "paleo" recharge to sustainable fresh groundwater yields has not been determined and evidence suggests that a large source of salinity at the distal end of the Mesilla Basin is saline discharge from deep groundwater flow. The magnitude and distribution of those deep saline flow paths are not determined. The contribution of deep groundwater to discharge and salinity in the shallow groundwater and surface water of the Mesilla Basin will be determined by collecting discrete groundwater samples and analyzing for aqueous geochemical and isotopic tracers, as well as the radioisotopes of argon and krypton. Analytes include major ions, trace elements, the stable isotopes of water, strontium and boron isotopes, uranium isotopes, the carbon isotopes of dissolved inorganic carbon, noble gas concentrations and helium isotope ratios. Dissolved gases are extracted and captured from groundwater wells using membrane contactors in a process known as ultra-trace sampling. Gas samples are analyzed for radioisotope ratios of krypton by the ATTA method and argon by low-level counting. Effectiveness of the ultra-trace sampling device and method was evaluated by comparing results of tritium concentrations to the krypton-85 content. Good agreement between the analyses, especially in samples with undetectable tritium, indicates that the ultra-trace procedure is effective and confirms that introduction of atmospheric air has not occurred. The geochemistry data indicate a complex system of geochemical

Contribution of water chemistry and fish condition to otolith chemistry: comparisons across salinity environments.

Science.gov (United States)

Izzo, C; Doubleday, Z A; Schultz, A G; Woodcock, S H; Gillanders, B M

2015-06-01

This study quantified the per cent contribution of water chemistry to otolith chemistry using enriched stable isotopes of strontium ((86) Sr) and barium ((137) Ba). Euryhaline barramundi Lates calcarifer, were reared in marine (salinity 40), estuarine (salinity 20) and freshwater (salinity 0) under different temperature treatments. To calculate the contribution of water to Sr and Ba in otoliths, enriched isotopes in the tank water and otoliths were quantified and fitted to isotope mixing models. Fulton's K and RNA:DNA were also measured to explore the influence of fish condition on sources of element uptake. Water was the predominant source of otolith Sr (between 65 and 99%) and Ba (between 64 and 89%) in all treatments, but contributions varied with temperature (for Ba), or interactively with temperature and salinity (for Sr). Fish condition indices were affected independently by the experimental rearing conditions, as RNA:DNA differed significantly among salinity treatments and Fulton's K was significantly different between temperature treatments. Regression analyses did not detect relations between fish condition and per cent contribution values. General linear models indicated that contributions from water chemistry to otolith chemistry were primarily influenced by temperature and secondly by fish condition, with a relatively minor influence of salinity. These results further the understanding of factors that affect otolith element uptake, highlighting the necessity to consider the influence of environment and fish condition when interpreting otolith element data to reconstruct the environmental histories of fish. © 2015 The Fisheries Society of the British Isles.

BENCHMARKING ORTEC ISOTOPIC MEASUREMENTS AND CALCULATIONS

Energy Technology Data Exchange (ETDEWEB)

Dewberry, R; Raymond Sigg, R; Vito Casella, V; Nitin Bhatt, N

2008-09-29

This report represents a description of compiled benchmark tests conducted to probe and to demonstrate the extensive utility of the Ortec ISOTOPIC {gamma}-ray analysis computer program. The ISOTOPIC program performs analyses of {gamma}-ray spectra applied to specific acquisition configurations in order to apply finite-geometry correction factors and sample-matrix-container photon absorption correction factors. The analysis program provides an extensive set of preset acquisition configurations to which the user can add relevant parameters in order to build the geometry and absorption correction factors that the program determines from calculus and from nuclear g-ray absorption and scatter data. The Analytical Development Section field nuclear measurement group of the Savannah River National Laboratory uses the Ortec ISOTOPIC analysis program extensively for analyses of solid waste and process holdup applied to passive {gamma}-ray acquisitions. Frequently the results of these {gamma}-ray acquisitions and analyses are to determine compliance with facility criticality safety guidelines. Another use of results is to designate 55-gallon drum solid waste as qualified TRU waste3 or as low-level waste. Other examples of the application of the ISOTOPIC analysis technique to passive {gamma}-ray acquisitions include analyses of standard waste box items and unique solid waste configurations. In many passive {gamma}-ray acquisition circumstances the container and sample have sufficient density that the calculated energy-dependent transmission correction factors have intrinsic uncertainties in the range 15%-100%. This is frequently the case when assaying 55-gallon drums of solid waste with masses of up to 400 kg and when assaying solid waste in extensive unique containers. Often an accurate assay of the transuranic content of these containers is not required, but rather a good defensible designation as >100 nCi/g (TRU waste) or <100 nCi/g (low level solid waste) is required. In

The effect of temperature, salinity and growth rate on the stable hydrogen isotopic composition of long chain alkenones produced by Emiliania huxleyi and Gephyrocapsa oceanica

Directory of Open Access Journals (Sweden)

S. Schouten

2006-01-01

Full Text Available Two haptophyte algae, Emiliania huxleyi and Gephyrocapsa oceanica, were cultured at different temperatures and salinities to investigate the impact of these factors on the hydrogen isotopic composition of long chain alkenones synthesized by these algae. Results showed that alkenones synthesized by G. oceanica were on average depleted in D by 30 compared to those of E. huxleyi when grown under similar temperature and salinity conditions. The fractionation factor, αalkenones-H2O, ranged from 0.760 to 0.815 for E. huxleyi and from 0.741 to 0.788 for G. oceanica. There was no significant correlation of αalkenones-H2O with temperature but a positive linear correlation was observed between αalkenones-H2O and salinity with ~3 change in fractionation per salinity unit and a negative correlation between αalkenones-H2O and growth rate. This suggests that both salinity and growth rate can have a substantial impact on the stable hydrogen isotopic composition of long chain alkenones in natural environments.

Reactor calculations in aid of isotope production at SAFARI-1

International Nuclear Information System (INIS)

Ball, G.

2003-01-01

Varying levels of reactor physics support is given to the isotope production industry. As the pressures on both the safety limits and economical production of reactor produced isotopes mount, reactor physics calculational support is playing an ever increasing role. Detailed modelling of the reactor, irradiation rigs and target material enables isotope production in reactors to be maximised with respect to yields and quality. NECSA's methodology in this field is described and some examples are given. (author)

Environmental isotope study related to groundwater age, flow system and saline water origin in Quaternary aquifers of North China Plain

International Nuclear Information System (INIS)

Zhang Zhigan; Payne, B.R.

1988-01-01

An isotopic hydrology section across the North China Plain has been studied to investigate problems of groundwater age, flow system and saline water origin in a semi-arid pre-mountain artesian basin. Two local and one regional flow system along the section have been recognized. Turnover time of water for alluvial fan, shallow and regional systems are estimated to be the order of 10 2 , 10 3 , and 10 4 years respectively. Specific flow rates for the three systems have been calculated. Only less than 5 percent of flow from alluvial fan is drained by the regional flow system and the rest, in natural conditions, discharges at surface in the front edge of an alluvial fan and forms a groundwater discharge belt at a good distance away from the mountain foot. Developed in the alluvial plain and coastal plain areas the shallow flow system embraces a series of small local systems. Groundwater in these systems appears to be the salt carrier during continental salinization. It washes salt out of the recharge area and deep-occurred strata by circulating and carries it up to the surface in lowland areas. Consequently, in parallel with salinization at surface a desalinization process occurs at depth, which provides an additional explanation for the existing thick deep fresh water zone in most arid and semi-arid regions, where continental salting process is in progress. (author). 6 refs, 8 figs, 4 tabs

Cl/Br ratios and chlorine isotope evidences for groundwater salinization and its impact on groundwater arsenic, fluoride and iodine enrichment in the Datong basin, China.

Science.gov (United States)

Li, Junxia; Wang, Yanxin; Xie, Xianjun

2016-02-15

In order to identify the salinization processes and its impact on arsenic, fluoride and iodine enrichment in groundwater, hydrogeochemical and environmental isotope studies have been conducted on groundwater from the Datong basin, China. The total dissolved solid (TDS) concentrations in groundwater ranged from 451 to 8250 mg/L, and 41% of all samples were identified as moderately saline groundwater with TDS of 3000-10,000 mg/L. The results of groundwater Cl concentrations, Cl/Br molar ratio and Cl isotope composition suggest that three processes including water-rock interaction, surface saline soil flushing, and evapotranspiration result in the groundwater salinization in the study area. The relatively higher Cl/Br molar ratio in groundwater from multiple screening wells indicates the contribution of halite dissolution from saline soil flushed by vertical infiltration to the groundwater salinization. However, the results of groundwater Cl/Br molar ratio model indicate that the effect of saline soil flushing practice is limited to account for the observed salinity variation in groundwater. The plots of groundwater Cl vs. Cl/Br molar ratio, and Cl vs δ(37)Cl perform the dominant effects of evapotranspiration on groundwater salinization. Inverse geochemical modeling results show that evapotranspiration may cause approximately 66% loss of shallow groundwater to account for the observed hydrochemical pattern. Due to the redox condition fluctuation induced by irrigation activities and evapotranspiration, groundwater salinization processes have negative effects on groundwater arsenic enrichment. For groundwater iodine and fluoride enrichment, evapotranspiration partly accounts for their elevation in slightly saline water. However, too strong evapotranspiration would restrict groundwater fluoride concentration due to the limitation of fluorite solubility. Copyright © 2015. Published by Elsevier B.V.

The calculation of isotopic partition function ratios by a perturbation theory technique

International Nuclear Information System (INIS)

Singh, G.; Wolfsberg, M.

1975-01-01

The vibrational Hamiltonian of a molecule in the harmonic approximation, H = (1/2) Σ (g/subi/jp/subi/p/subj/ + f/subi/jq/subi/q/subj/), has been divided into a diagonal part (terms with i=j) and an off-diagonal part (inot-equalj), which is regarded as the perturbation. The vibrational partition function of the molecule is then calculated by Schwinger perturbation theory as the partition function of the unperturbed problem, corresponding to a collection of oscillators with frequencies 2πν/subi/' = (f/subi/ig/subi/i)/sup 1 / 2 /, plus perturbation correction terms which are calculated to second order. With the usual assumptions of isotope effect calculations that the molecular translations and rotations are classical and separable from the vibrations, the perturbation formulation of the vibrational partition function is easily transformed into a perturbation theory formulation of (reduced) isotopic partition function ratios. If, for example, the molecular potential function is expressed in terms of the displacements of bond stretches and bond angle bends from their respective equilibrium values, the unperturbed partition function ratio corresponds to the isotope effect expected for noninteracting bond-stretch and bond-angle-bend oscillators. Detailed comparison is made for a number of molecular systems of perturbation theory calculations of partition functions and isotopic partition function ratios with exact calculations carried out by actually obtaining the normal mode vibrational frequencies of the vibrational Hamiltonian. Good agreement is found. The utility of the perturbation theory formulation resides in the fact that it permits one to look at isotope effects in a very simple manner; some demonstrations are given

Coastal groundwater salinization: Focus on the vertical variability in a multi-layered aquifer through a multi-isotope fingerprinting (Roussillon Basin, France)

Energy Technology Data Exchange (ETDEWEB)

Petelet-Giraud, Emmanuelle, E-mail: e.petelet@brgm.fr [BRGM, Avenue C. Guillemin, BP 36009, 45060 Orléans Cedex 02 (France); Négrel, Philippe [BRGM, Avenue C. Guillemin, BP 36009, 45060 Orléans Cedex 02 (France); Aunay, Bertrand [BRGM, Réunion Agency, 5, rue Sainte-Anne, CS 51016, 97404 Saint Denis Cedex (France); Ladouche, Bernard; Bailly-Comte, Vincent [BRGM Montpellier Agency, 1039, rue de Pinville, 34000 Montpellier (France); Guerrot, Catherine; Flehoc, Christine [BRGM, Avenue C. Guillemin, BP 36009, 45060 Orléans Cedex 02 (France); Pezard, Philippe; Lofi, Johanna [Géosciences Montpellier, UMR 5243, Université de Montpellier, cc069, Place Eugène Bataillon, 34095 Montpellier Cedex 05 (France); Dörfliger, Nathalie [BRGM, Avenue C. Guillemin, BP 36009, 45060 Orléans Cedex 02 (France)

2016-10-01

The Roussillon sedimentary Basin (South France) is a complex multi-layered aquifer, close to the Mediterranean Sea facing seasonally increases of water abstraction and salinization issues. We report geochemical and isotopic vertical variability in this aquifer using groundwater sampled with a Westbay System® at two coastal monitoring sites: Barcarès and Canet. The Westbay sampling allows pointing out and explaining the variation of water quality along vertical profiles, both in productive layers and in the less permeable ones where most of the chemical processes are susceptible to take place. The aquifer layers are not equally impacted by salinization, with electrical conductivity ranging from 460 to 43,000 μS·cm{sup −1}. The δ{sup 2}H–δ{sup 18}O signatures show mixing between seawater and freshwater components with long water residence time as evidenced by the lack of contribution from modern water using {sup 3}H, {sup 14}C and CFCs/SF6. S(SO{sub 4}) isotopes also evidence seawater contribution but some signatures can be related to oxidation of pyrite and/or organically bounded S. In the upper layers {sup 87}Sr/{sup 86}Sr ratios are close to that of seawater and then increase with depth, reflecting water–rock interaction with argillaceous formations while punctual low values reflect interaction with carbonate. Boron isotopes highlight secondary processes such as adsorption/desorption onto clays in addition to mixings. At the Barcarès site (120 m deep), the high salinity in some layers appear to be related neither to present day seawater intrusion, nor to Salses-Leucate lagoonwater intrusion. Groundwater chemical composition thus highlights binary mixing between fresh groundwater and inherited salty water together with cation exchange processes, water–rock interactions and, locally, sedimentary organic matter mineralisation probably enhanced by pyrite oxidation. Finally, combining the results of this study and those of Caballero and Ladouche (2015

Criticality reference benchmark calculations for burnup credit using spent fuel isotopics

International Nuclear Information System (INIS)

Bowman, S.M.

1991-04-01

To date, criticality analyses performed in support of the certification of spent fuel casks in the United States do not take credit for the reactivity reduction that results from burnup. By taking credit for the fuel burnup, commonly referred to as ''burnup credit,'' the fuel loading capacity of these casks can be increased. One of the difficulties in implementing burnup credit in criticality analyses is that there have been no critical experiments performed with spent fuel which can be used for computer code validation. In lieu of that, a reference problem set of fresh fuel critical experiments which model various conditions typical of light water reactor (LWR) transportation and storage casks has been identified and used in the validation of SCALE-4. This report documents the use of this same problem set to perform spent fuel criticality benchmark calculations by replacing the actual fresh fuel isotopics from the experiments with six different sets of calculated spent fuel isotopics. The SCALE-4 modules SAS2H and CSAS4 were used to perform the analyses. These calculations do not model actual critical experiments. The calculated k-effectives are not supposed to equal unity and will vary depending on the initial enrichment and burnup of the calculated spent fuel isotopics. 12 refs., 11 tabs

Technical note: Consistent calculation of aquatic gross production from oxygen triple isotope measurements

Directory of Open Access Journals (Sweden)

J. Kaiser

2011-07-01

Full Text Available Oxygen triple isotope measurements can be used to calculate aquatic gross oxygen production rates. Past studies have emphasised the appropriate definition of the ¹⁷O excess and often used an approximation to derive production rates from the ¹⁷O excess. Here, I show that the calculation can be phrased more consistently and without any approximations using the relative ¹⁷O/¹⁶O and ¹⁸O/¹⁶O isotope ratio differences (delta values directly. I call this the "dual delta method". The ¹⁷O excess is merely a mathematical construct and the derived production rate is independent of its definition, provided all calculations are performed with a consistent definition. I focus on the mixed layer, but also show how time series of triple isotope measurements below the mixed layer can be used to derive gross production.

In the calculation of mixed layer productivity, I explicitly include isotopic fractionation during gas invasion and evasion, which requires the oxygen supersaturation s to be measured as well. I also suggest how bubble injection could be considered in the same mathematical framework. I distinguish between concentration steady state and isotopic steady state and show that only the latter needs to be assumed in the calculation. It is even possible to derive an estimate of the net production rate in the mixed layer that is independent of the assumption of concentration steady state.

I review measurements of the parameters required for the calculation of gross production rates and show how their systematic uncertainties as well as the use of different published calculation methods can cause large variations in the production rates for the same underlying isotope ratios. In particular, the ¹⁷O excess of dissolved O₂ in equilibrium with atmospheric O₂ and the ¹⁷O excess of photosynthetic O₂ need to

Normal coordinate treatment of liquid water and calculation of vapor pressure isotope effects

International Nuclear Information System (INIS)

Gellai, B.; Van Hook, W.A.

1983-01-01

A vibrational analysis of liquid water is reported, assuming a completely hydrogen-bonded network with continuously varying strengths of the hydrogen bonds. Frequency distribution calculations are made for intramolecular stretching and bending modes and for the intramolecular frequency region. The calculated distributions are compared with the experimental spectroscopic ones. As another test, vapor pressure isotope effects are calculated from the theoretical distributions for some isotopic water molecules. Results are compared with those of other authors obtained from a mixture model. (author)

The hydrogeochemical and isotopic investigations of the two-layered Shiraz aquifer in the northwest of Maharlou saline lake, south of Iran

Science.gov (United States)

Tajabadi, Mehdi; Zare, Mohammad; Chitsazan, Manouchehr

2018-03-01

Maharlou saline lake is the outlet of Shiraz closed basin in southern Iran, surrounded by several disconnected alluvial fresh water aquifers. These aquifers in the west and northwest of the lake are recharged by karstic anticlines such as Kaftarak in the north and Barmshour in the south. Here groundwater salinity varies along the depth so that better quality water is located below brackish or saline waters. The aim of this study is to investigate the reason for the salinity anomaly and the origin of the fresher groundwater in lower depth. Hence, the change in groundwater salinity along depth has been investigated by means of a set of geoelectrical, hydrogeological, hydrogeochemical, and environmental isotopes data. The interpretation of geoelectrical profiles and hydrogeological data indicates that the aquifer in the southeast of Shiraz plain is a two-layer aquifer separated by a fine-grained (silt and clay) layer with an approximate thickness of 40 m at the depth of about 100-120 m. Hydrgeochemistry showed that the shallow aquifer is recharged by Kaftarak karstic anticline and is affected by the saline lake water. The lake water fraction varies in different parts from zero for shallow aquifer close to the karstic anticlines to ∼70 percent in the margin of the lake. The deep aquifer is protected from the intrusion of saline lake water due to the presence of the above-mentioned confining layer with lake water fraction of zero. The stable isotopes signatures also indicate that the 'fresh' groundwater belonging to the deep aquifer is not subject to severe evaporation or mixing which is typical of the karstic water of the area. It is concluded that the characteristics of the deep aquifer are similar to those of the karstic carbonate aquifer. This karstic aquifer is most probably the Barmshour carbonated anticline buried under the shallow aquifer in the southern part. It may also be the extension of the Kaftarak anticline in the northern part.

Isotope Production Facility Conceptual Thermal-Hydraulic Design Review and Scoping Calculations

International Nuclear Information System (INIS)

Pasamehmetoglu, K.O.; Shelton, J.D.

1998-01-01

The thermal-hydraulic design of the target for the Isotope Production Facility (IPF) is reviewed. In support of the technical review, scoping calculations are performed. The results of the review and scoping calculations are presented in this report

Calculation of Site-specific Carbon-isotope Fractionation in Pedogenic Oxide Minerals

Energy Technology Data Exchange (ETDEWEB)

Rustad, James R.; Zarzycki, Piotr

2008-07-29

Ab initio molecular dynamics and quantum chemistry techniques are used to calculate the structure, vibrational frequencies, and carbon-isotope fractionation factors of the carbon dioxide component [CO2(m)] of soil (oxy)hydroxide minerals goethite, diaspore, and gibbsite. We have identified two possible pathways of incorporation of CO2(m) into (oxy)hydroxide crystal structures: one in which the C4+ substitutes for four H+ [CO2(m)A] and another in which C4+ substitutes for (Al3+,Fe3+) + H+ [CO2(m)B]. Calculations of isotope fractionation factors give large differences between the two structures, with the CO2(m)A being isotopically lighter than CO2(m)B by ≈10 per mil in the case of gibbsite and nearly 20 per mil in the case of goethite. The reduced partition function ratio of CO2(m)B structure in goethite differs from CO2(g) by <1 per mil. The predicted fractionation for gibbsite is >10 per mil higher, close to those measured for calcite and aragonite. The surprisingly large difference in the carbon-isotope fractionation factor between the CO2(m)A and CO2(m)B structures within a given mineral suggests that the isotopic signatures of soil (oxy)hydroxide could be heterogeneous.

A numerical scheme to calculate temperature and salinity dependent air-water transfer velocities for any gas

Science.gov (United States)

Johnson, M. T.

2010-02-01

The transfer velocity determines the rate of exchange of a gas across the air-water interface for a given deviation from Henry's law equilibrium between the two phases. In the thin film model of gas exchange, which is commonly used for calculating gas exchange rates from measured concentrations of trace gases in the atmosphere and ocean/freshwaters, the overall transfer is controlled by diffusion-mediated films on either side of the air-water interface. Calculating the total transfer velocity (i.e. including the influence from both molecular layers) requires the Henry's law constant and the Schmidt number of the gas in question, the latter being the ratio of the viscosity of the medium and the molecular diffusivity of the gas in the medium. All of these properties are both temperature and (on the water side) salinity dependent and extensive calculation is required to estimate these properties where not otherwise available. The aim of this work is to standardize the application of the thin film approach to flux calculation from measured and modelled data, to improve comparability, and to provide a numerical framework into which future parameter improvements can be integrated. A detailed numerical scheme is presented for the calculation of the gas and liquid phase transfer velocities (ka and kw respectively) and the total transfer velocity, K. The scheme requires only basic physical chemistry data for any gas of interest and calculates K over the full range of temperatures, salinities and wind-speeds observed in and over the ocean. Improved relationships for the wind-speed dependence of ka and for the salinity-dependence of the gas solubility (Henry's law) are derived. Comparison with alternative schemes and methods for calculating air-sea flux parameters shows good agreement in general but significant improvements under certain conditions. The scheme is provided as a downloadable program in the supplementary material, along with input files containing molecular

Stable isotope studies of some low enthalpy geothermal systems in Kenya

Science.gov (United States)

Tole, Mwakio P.

Oxygen and hydrogen isotope compositions of some low enthalpy geothermal systems in Kenya have been determined. Plots on δ 18O versus δD diagrams show that the compositions do not deviate appreciably from local meteoric water values. This would indicate that local meteoric waters are heated at depth and rise to the surface without much interaction with the country rocks. This is interpreted to be the case for the geothermal systems at Majimoto and Narosura, which have salinities of less than 350 ppm TDS and calculated reservoir temperatures of less than 110°C. The geothermal systems at Kapedo and Homa mountain which have high salinities (> 2 000 ppm TDS) and relatively higher calculated reservoir temperatures (> 150° C) are interpreted to have been operating for long periods of time, such that the rocks through which the present day geothermal waters are circulating have attained isotopic equilibrium with local meteoric waters.

Calculation of prompt neutron spectra for curium isotopes

Energy Technology Data Exchange (ETDEWEB)

Ohsawa, Takaaki [Kinki Univ., Higashi-Osaka, Osaka (Japan). Atomic Energy Research Inst.

1997-03-01

With the aim of checking the existing evaluations contained in JENDL-3.2 and providing new evaluations based on a methodology proposed by the author, a series of calculations of prompt neutron spectra have been undertaken for curium isotopes. Some of the evaluations in JENDL-3.2 was found to be unphysically hard and should be revised. (author)

Identification of the mechanisms and origin of salinization of groundwaters in coastal aquifers by means of isotopic techniques

International Nuclear Information System (INIS)

Araguas, L. J.; Quejido, A. J.

2007-01-01

To study the origin of salinity and the mechanisms operating in coastal aquifers, a set of tools is available to determine the essential aspects of the hydrogeological behaviour of the system. these tools are based on the integrated use of hydrochemical parameters (major constituents and trace elements) and isotopic parameters (oxygen, hydrogen, sulfur, carbon, strontium and boron). In addition to the active intrusion of seawater, salinization in coastal areas may be influenced by various human activities that accelerate the degradation of water quality, such as concentrated pumping, intensive farming techniques with return of irrigation water, or reuse of urban and industrial waste water. Characterization of the dominant processes and mechanisms is required for suitable management of the resource and implementation of corrective measures. (Author)

Calculation of radiation production of high specific activity isotopes 192Ir and 60Co

International Nuclear Information System (INIS)

Zhou Quan; Zhong Wenfa; Xu Xiaolin

1997-01-01

The high specific activity isotopes: 192 Ir and 60 Co in the high neutron flux reactor are calculated with the method of reactor physics. The results of calculation are analyzed in two aspects: the production of isotopes and the influence to parameters of the reactor, and hence a better case is proposed as a reference to the production

Sr ISOTOPIC EVIDENCE FOR STUDYING THE SALINIZATION OF SOILS: AN EXAMPLE FROM THE SAN VITALE PINEWOOD (RAVENNA

Directory of Open Access Journals (Sweden)

Umberto Masi

2009-12-01

Full Text Available In the frame of a multidisciplinary project of research on the San Vitale Pinewood ecosystem, north of Ravenna, the Sr isotope study of a soil profile developed on an old coastal dune aiming at detecting the effect of salinization is presented. The Sr isotope ratios of the bulk soil samples decreased significantly from upper (0.717 to lower (0.712 horizons because of the abundant marine salts deposited by the brackish water present in the deep soil. While the main source of Sr in the upper horizons is the silicates, especially the feldspaths contained in the old dune sediments; in contrast, Sr in the lower horizons is significantly also of evaporitic origin (0.707-0.709. This latter is dominantly the strontium bio-available to the plants.

Marine water from mid-Holocene sea level highstand trapped in a coastal aquifer: Evidence from groundwater isotopes, and environmental significance

Energy Technology Data Exchange (ETDEWEB)

Lee, Stephen [School of Civil, Environmental and Chemical Engineering, RMIT University, Melbourne (Australia); Currell, Matthew, E-mail: Matthew.currell@rmit.edu.au [School of Civil, Environmental and Chemical Engineering, RMIT University, Melbourne (Australia); Cendón, Dioni I. [Australian Nuclear Science and Technology Organisation, Kirrawee (Australia); Connected Water Initiative, School of Biological, Earth and Environmental Sciences, University of New South Wales (UNSW), Sydney (Australia)

2016-02-15

A multi-layered coastal aquifer in southeast Australia was assessed using environmental isotopes, to identify the origins of salinity and its links to palaeo-environmental setting. Spatial distribution of groundwater salinity (electrical conductivity values ranging from 0.395 to 56.1 mS/cm) was examined along the coastline along with geological, isotopic and chemical data. This allowed assessment of different salinity sources and emplacement mechanisms. Molar chloride/bromide ratios range from 619 to 1070 (621 to 705 in samples with EC > 15 mS/cm), indicating salts are predominantly marine. Two distinct vertical salinity profiles were observed, one with increasing salinity with depth and another with saline shallow water overlying fresh groundwater. The saline shallow groundwater (EC = 45.4 to 55.7 mS/cm) has somewhat marine-like stable isotope ratios (δ{sup 18}O = − 2.4 to − 1.9 ‰) and radiocarbon activities indicative of middle Holocene emplacement (47.4 to 60.4 pMC). This overlies fresher groundwater with late Pleistocene radiocarbon ages and meteoric stable isotopes (δ{sup 18}O = − 5.5 to − 4.6‰). The configuration suggests surface inundation of the upper sediments by marine water during the mid-Holocene (c. 2–8 kyr BP), when sea level was 1–2 m above today's level. Profiles of chloride, stable isotopes, and radiocarbon indicate mixing between this pre-modern marine water and fresh meteoric groundwater to varying degrees around the coastline. Mixing calculations using chloride and stable isotopes show that in addition to fresh-marine water mixing, some salinity is derived from transpiration by halophytic vegetation (e.g. mangroves). The δ{sup 13}C ratios in saline water (− 17.6 to − 18.4‰) also have vegetation/organic matter signatures, consistent with emplacement by surface inundation and extensive interaction between vegetation and recharging groundwater. Saline shallow groundwater is preserved only in areas where low

Hartree-Fock calculation of nuclear binding energy of sodium isotopes

International Nuclear Information System (INIS)

Campi, X.; Flocard, H.

1975-01-01

Mass spectrometer measurements of the neutron rich sodium isotopes show a sudden increase at 31 Na in the values of the two neutron separation energies. The spherical shell model naturally predicts a sudden decrease at 32 Na after the N=20 shell closure. It is proposed that the explanation for this disagreement lies in the fact that sodium isotopes in this mass region are strongly deformed due to the filling of negative parity orbitals from the 1f(7/2) shell. Hartree-Fock calculations are presented in support of this conjecture [fr

Study of multiplication factor sensitivity to the spread of WWER spent fuel isotopics calculated by different codes

International Nuclear Information System (INIS)

Markova, L.

2001-01-01

As a sensitivity study the impact on the system reactivity was studied in the case that different calculational methodologies of spent fuel isotopic concentrations were used for WWER spent fuel inventory computations. The sets of isotopic concentrations obtained by calculations with different codes and libraries as a result of the CB2 international benchmark focused on WWER-440 burnup credit were used to show the spread of the calculated spent fuel system reactivity. Using the MCNP 4B code and changing the isotopics input data, the multiplication factor of an infinite array of the WWER-440 fuel pin cells was calculated. The evaluation of the results shows the sensitivity of the calculated reactivity to different calculational methodologies used for the spent fuel inventory computation. In the studied cases of the CB2 benchmark, the spread of the reference k-results relative to the mean was found less or about ±1% in spite of the fact that the data of isotopic concentrations were spread much more. (author)

Calculation of isotopic mass and energy production by a matrix operator method

International Nuclear Information System (INIS)

Lee, C.E.

1976-08-01

The Volterra method of the multiplicative integral is used to determine the isotopic density, mass, and energy production in linear systems. The solution method, assumptions, and limitations are discussed. The method allows a rapid accurate calculation of the change in isotopic density, mass, and energy production independent of the magnitude of the time steps, production or decay rates, or flux levels

Forward Modeling of Carbonate Proxy Data from Planktonic Foraminifera using Oxygen Isotope Tracers in a Global Ocean Model

Science.gov (United States)

Schmidt, Gavin A.

1999-01-01

The distribution and variation of oxygen isotopes in seawater are calculated using the Goddard Institute for Space Studies global ocean model. Simple ecological models are used to estimate the planktonic foraminiferal abundance as a function of depth, column temperature, season, light intensity, and density stratification. These models are combined to forward model isotopic signals recorded in calcareous ocean sediment. The sensitivity of the results to the changes in foraminiferal ecology, secondary calcification, and dissolution are also examined. Simulated present-day isotopic values for ecology relevant for multiple species compare well with core-top data. Hindcasts of sea surface temperature and salinity are made from time series of the modeled carbonate isotope values as the model climate changes. Paleoclimatic inferences from these carbonate isotope records are strongly affected by erroneous assumptions concerning the covariations of temperature, salinity, and delta (sup 18)O(sub w). Habitat-imposed biases are less important, although errors due to temperature-dependent abundances can be significant.

Relationships of stable isotopes, water-rock interaction and salinization in fractured aquifers, Petrolina region, Pernambuco State, Brazil

Energy Technology Data Exchange (ETDEWEB)

Silva, Priscila Sousa, E-mail: priscila.silva@cprm.gov.br [Serviço Geológico do Brasil (CPRM), Manaus, AM (Brazil); Campos, José Eloi Guimarães; Cunha, Luciano Soares; Mancini, Luís Henrique, E-mail: eloi@unb.br, E-mail: lucianosc@unb.br, E-mail: lmancini@unb.br [Universidade de Brasília (UnB), Brasília, DF (Brazil)

2018-01-15

The Petrolina County, Pernambuco State, Brazil, presents specificities that make it unique from a hydrogeological point of view. Water resource scarcity is both a quantitative and qualitative issue. The climate is classified as semiarid, having low precipitation, along with high temperatures and evapotranspiration rates. Aquifer zones are related to low connected fractures resulting in a restricted water flow in the aquifer. The recharge is limited and the groundwater salinity is high. Stable isotope analyses of H and O were developed in groundwater samples (with different electrical conductivity) and surface water collected in a bypass channel flowing from the São Francisco River. The results were plotted in a δD ‰ versus δ{sup 18}O ‰ graph along with the curves of the global and local meteoric water line. Groundwater samples showed unexpected results showing a lighter sign pattern when compared to the meteoric waters. More negative δD and δ{sup 18}O values indicate an enrichment in light isotopes, which show that this process is not influenced by surface processes, where the enrichment occurs in heavy isotopes due to evaporation. The isotopic signature observed is interpreted either as resulting from the water-rock interaction, or as resulting from recharge from paleo rains. The waters are old and show restricted flow. So the water-rock contact time is extended. In the rock weathering processes, through the hydration of feldspars, there is preferential assimilation of heavy isotopes at the expense of the lighter ones that remain in the water. Analyses of the {sup 87}Sr/{sup 86}Sr ratio and isotopic groundwater dating assist in the interpretations. (author)

A thoroughly validated spreadsheet for calculating isotopic abundances (H-2, O-17, O-18) for mixtures of waters with different isotopic compositions

NARCIS (Netherlands)

Faghihi, V.; Meijer, H. A. J.; Groening, Manfred

2015-01-01

RationaleOxygen and hydrogen stable isotopes are widely used tracers for studies on naturally occurring and laboratory mixtures of isotopically different waters. Although the mixing calculations are straightforward to perform, there are ample possibilities to make mistakes, especially when dealing

Calculation of the isotope concentrations, source terms and radiation shielding of the SAFARI-1 irradiation products

International Nuclear Information System (INIS)

Stoker, C.C.; Ball, G.

2000-01-01

The ever increasing expansion of the irradiation product portfolio of the SAFARI-1 reactor leads to the need to routinely calculate the radio-isotope concentrations and source terms for the materials irradiated in the reactor accurately. In addition to this, the required shielding for the transportation and processing of these irradiation products needs to be determined. In this paper the calculational methodology applied is described with special attention given to the spectrum dependence of the one-group cross sections of selected SAFARI-1 irradiation materials and the consequent effect on the determination of the isotope concentrations and source terms. Comparisons of the calculated isotopic concentrations and dose rates with experimental analysis and measurements provide confidence in the calculational methodologies and data used. (author)

FABGEN, a transient power-generation and isotope birth rate calculator

International Nuclear Information System (INIS)

Roland, H.C.

1975-04-01

A description is given of the FABGEN program, a fast-running program for calculating fuel element power-generation rates and selected fission product birth rates in a known neutron flux as functions of time. A first forward difference calculation is used, and the time step is one day. Provisions are made for including various fuel element lengths, variation of thermal flux with time, and use of different fertile isotopes. Five different fission products may be specified for birth-rate calculations. A daily summary may be output, or totals by days may be accumulated for final output. (U.S.)

Identifying Stereoisomers by ab-initio Calculation of Secondary Isotope Shifts on NMR Chemical Shieldings

Directory of Open Access Journals (Sweden)

Karl-Heinz Böhm

2014-04-01

Full Text Available We present ab-initio calculations of secondary isotope effects on NMR chemical shieldings. The change of the NMR chemical shift of a certain nucleus that is observed if another nucleus is replaced by a different isotope can be calculated by computing vibrational corrections on the NMR parameters using electronic structure methods. We demonstrate that the accuracy of the computational results is sufficient to even distinguish different conformers. For this purpose, benchmark calculations for fluoro(2-2Hethane in gauche and antiperiplanar conformation are carried out at the HF, MP2 and CCSD(T level of theory using basis sets ranging from double- to quadruple-zeta quality. The methodology is applied to the secondary isotope shifts for 2-fluoronorbornane in order to resolve an ambiguity in the literature on the assignment of endo- and exo-2-fluoronorbornanes with deuterium substituents in endo-3 and exo-3 positions, also yielding insight into mechanistic details of the corresponding synthesis.

Identifying stereoisomers by ab-initio calculation of secondary isotope shifts on NMR chemical shieldings.

Science.gov (United States)

Böhm, Karl-Heinz; Banert, Klaus; Auer, Alexander A

2014-04-23

We present ab-initio calculations of secondary isotope effects on NMR chemical shieldings. The change of the NMR chemical shift of a certain nucleus that is observed if another nucleus is replaced by a different isotope can be calculated by computing vibrational corrections on the NMR parameters using electronic structure methods. We demonstrate that the accuracy of the computational results is sufficient to even distinguish different conformers. For this purpose, benchmark calculations for fluoro(2-2H)ethane in gauche and antiperiplanar conformation are carried out at the HF, MP2 and CCSD(T) level of theory using basis sets ranging from double- to quadruple-zeta quality. The methodology is applied to the secondary isotope shifts for 2-fluoronorbornane in order to resolve an ambiguity in the literature on the assignment of endo- and exo-2-fluoronorbornanes with deuterium substituents in endo-3 and exo-3 positions, also yielding insight into mechanistic details of the corresponding synthesis.

Interacting boson model: Microscopic calculations for the mercury isotopes

Energy Technology Data Exchange (ETDEWEB)

Druce, C.H.; Pittel, S.; Barrett, B.R.; Duval, P.D.

1987-05-15

Microscopic calculations of the parameters of the proton--neutron interacting boson model (IBM-2) appropriate to the even Hg isotopes are reported. The calculations are based on the Otsuka--Arima--Iachello boson mapping procedure, which is briefly reviewed. Renormalization of the parameters due to exclusion of the l = 4 g boson is treated perturbatively. The calculations employ a semi-realistic shell-model Hamiltonian with no adjustable parameters. The calculated parameters of the IBM-2 Hamiltonian are used to generate energy spectra and electromagnetic transition probabilities, which are compared with experimental data and with the result of phenomenological fits. The overall agreement is reasonable with some notable exceptions, which are discussed. Particular attention is focused on the parameters of the Majorana interaction and on the F-spin character of low-lying levels. copyright 1987 Academic Press, Inc.

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)

Desiccation-crack-induced salinization in deep clay sediment

Directory of Open Access Journals (Sweden)

S. Baram

2013-04-01

Full Text Available A study on water infiltration and solute transport in a clayey vadose zone underlying a dairy farm waste source was conducted to assess the impact of desiccation cracks on subsurface evaporation and salinization. The study is based on five years of continuous measurements of the temporal variation in the vadose zone water content and on the chemical and isotopic composition of the sediment and pore water in it. The isotopic composition of water stable isotopes (δ18O and δ2H in water and sediment samples, from the area where desiccation crack networks prevail, indicated subsurface evaporation down to ~ 3.5 m below land surface, and vertical and lateral preferential transport of water, following erratic preferential infiltration events. Chloride (Cl− concentrations in the vadose zone pore water substantially increased with depth, evidence of deep subsurface evaporation and down flushing of concentrated solutions from the evaporation zones during preferential infiltration events. These observations led to development of a desiccation-crack-induced salinization (DCIS conceptual model. DCIS suggests that thermally driven convective air flow in the desiccation cracks induces evaporation and salinization in relatively deep sections of the subsurface. This conceptual model supports previous conceptual models on vadose zone and groundwater salinization in fractured rock in arid environments and extends its validity to clayey soils in semi-arid environments.

CRYOCOL a computer program to calculate the cryogenic distillation of hydrogen isotopes

International Nuclear Information System (INIS)

Douglas, S.R.

1993-02-01

This report describes the computer model and mathematical method coded into the AECL Research computer program CRYOCOL. The purpose of CRYOCOL is to calculate the separation of hydrogen isotopes by cryogenic distillation. (Author)

Ab initio calculations of the Fe(II) and Fe(III) isotopic effects in citrates, nicotianamine, and phytosiderophore, and new Fe isotopic measurements in higher plants

Science.gov (United States)

Moynier, Frédéric; Fujii, Toshiyuki; Wang, Kun; Foriel, Julien

2013-05-01

Iron is one of the most abundant transition metal in higher plants and variations in its isotopic compositions can be used to trace its utilization. In order to better understand the effect of plant-induced isotopic fractionation on the global Fe cycling, we have estimated by quantum chemical calculations the magnitude of the isotopic fractionation between different Fe species relevant to the transport and storage of Fe in higher plants: Fe(II)-citrate, Fe(III)-citrate, Fe(II)-nicotianamine, and Fe(III)-phytosiderophore. The ab initio calculations show firstly, that Fe(II)-nicotianamine is ˜3‰ (56Fe/54Fe) isotopically lighter than Fe(III)-phytosiderophore; secondly, even in the absence of redox changes of Fe, change in the speciation alone can create up to ˜1.5‰ isotopic fractionation. For example, Fe(III)-phytosiderophore is up to 1.5‰ heavier than Fe(III)-citrate2 and Fe(II)-nicotianamine is up to 1‰ heavier than Fe(II)-citrate. In addition, in order to better understand the Fe isotopic fractionation between different plant components, we have analyzed the iron isotopic composition of different organs (roots, seeds, germinated seeds, leaves and stems) from six species of higher plants: the dicot lentil (Lens culinaris), and the graminaceous monocots Virginia wild rye (Elymus virginicus), Johnsongrass (Sorghum halepense), Kentucky bluegrass (Poa pratensis), river oat (Uniola latifolia), and Indian goosegrass (Eleusine indica). The calculations may explain that the roots of strategy-II plants (Fe(III)-phytosiderophore) are isotopically heavier (by about 1‰ for the δ56Fe) than the upper parts of the plants (Fe transported as Fe(III)-citrate in the xylem or Fe(II)-nicotianamine in the phloem). In addition, we suggest that the isotopic variations observed between younger and older leaves could be explained by mixing of Fe received from the xylem and the phloem.

Gypsum Formation during the Messinian Salinity Crisis: an Alternative Model

Science.gov (United States)

Grothe, A.; Krijgsman, W.; Sangiorgi, F.; Vasiliev, I.; Baak, C. V.; Wolthers, M.; Stoica, M.; Reichart, G. J.; Davies, G.

2016-12-01

During the Messinian Salinity Crisis (MSC; 5.97 - 5.33 Myr ago), thick packages of evaporites (gypsum and halite) were deposited in the Mediterranean Basin. Traditionally, the occurrence of these evaporites is explained by the so-called "desiccation-model", in which evaporites are considered to result from a (partly) desiccated basin. In the last decade, it was thought that changes in the Mediterranean-Atlantic connectivity could explain the formation of gypsum. Stable isotope studies, however, show that the gypsum formed under influence of large freshwater input. Here we present new strontium isotope data from two well-dated Messinian sections in the Black and Caspian Seas. Our Sr isotope records suggest a persistent Mediterranean-Black Sea connection throughout the salinity crisis, which implies a large additional freshwater source to the Mediterranean. We claim that low saline waters from the Black Sea region are a prerequisite for gypsum formation in the Mediterranean and speculate about the mechanisms explaining this apparent paradox.

Salinization mechanisms in semi-arid regions

International Nuclear Information System (INIS)

Santiago, M.M.F.

1984-01-01

During a period of three years the basins of the Pereira de Miranda and Caxitore dams, located in the crystalline rock area of Ceara, Brazil, were studied in order to determine the mechanisms of salinization of their waters. Isotope methods ( 18 O/ 16 O) and hidrochemistry (determination of the of the maior ions) were applied to surface, underground and rain water in this study. An isotope model was designed and applied to the determination of evaporation and percolation of dams in semi-arid zones during the dry season. The results are compared to those from a conventional chemical model. As causes of salinization of the water in the dams, the contributions of the rain itself and the lixiviation of the soil are quantified. An interaction between the dams and the underground water is imperceptible. The salinization of the underground water is attributed to recharge of the aquifer with rain water from the surface runoff followed by evaporation of the water rising, due to capilarity, in a one-directional flow to the surface. (Author) [pt

The interacting boson model: Microscopic calculations for the mercury isotopes

Science.gov (United States)

Druce, C. H.; Pittel, S.; Barrett, B. R.; Duval, P. D.

1987-05-01

Microscopic calculations of the parameters of the proton-neutron interacting boson model (IBM-2) appropriate to the even Hg isotopes are reported. The calculations are based on the Otsuka-Armia-Iachello boson mapping procedure, which is briefly reviewed. Renormalization of the parameters due to exclusion of the l=4 g boson is treated perturbatively. The calculations employ a semi-realistic shell-model Hamiltonian with no adjustable parameters. The calculated parameters of the IBM-2 Hamiltonian are used to generate energy spectra and electromagnetic transition probabilities, which are compared with experimental data and with the result of phenomenological fits. The overall agreement is reasonable with some notable exceptions, which are discussed. Particular attention is focused on the parameters of the Majorana interaction and on the F-spin character of low-lying levels.

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-09-15

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

Calculation of nucleon densities in calcium, nickel, and molybdenum isotopes on the basis of the dispersive optical model

Science.gov (United States)

Bespalova, O. V.; Klimochkina, A. A.

2017-09-01

The radial distributions of proton and neutron densities in the even-even isotopes 40-70Ca and 48-78Ni and the analogous distributions of neutron densities in the even-even isotopes 92-138Mo were calculated on the basis of the mean-fieldmodel involving a dispersive optical potential. The respective root-mean-square radii and neutron-skin thicknesses were determined for the nuclei under study. In N > 40 calcium isotopes, the calculated neutron root-mean-square radius exhibits a fast growth with increasing N, and this is consistent with the prediction of the neutron-halo structure in calcium isotopes near the neutron drip line.

An IBM-1620 code for calculation of isotopic composition of irradiated thorium (ISOCOM-2)

International Nuclear Information System (INIS)

Soliman, R.H.; Karchava, G.; Hamouda, I.

1978-01-01

The present work gives a description of an IBM-1620 code to calculate the isotopic composition during the irradiation of a nuclear fuel, which initially contains 232 Th. The numerical results on test calculations are presented. The code has been in operation since 1968

Tracing groundwater salinization processes in coastal aquifers: a hydrogeochemical and isotopic approach in Na-Cl brackish waters of north-western Sardinia, Italy

Science.gov (United States)

Mongelli, G.; Monni, S.; Oggiano, G.; Paternoster, M.; Sinisi, R.

2013-01-01

In the Mediterranean area the demand of good quality water is often threatened by salinization, especially in coastal areas. The salinization is the result of concomitant processes due to both marine water intrusion and rock-water interaction, which in some cases are hardly distinguishable. In northwestern Sardinia, in the Nurra area, salinization due to marine water intrusion has been recently evidenced as consequence of bore hole exploitation. However, the geology of the Nurra records a long history from Paleozoic to Quaternary, resulting in relative structural complexity and in a wide variety of lithologies, including Triassic evaporites. To elucidate the origin of the saline component in the Nurra aquifer, may furnish a useful and more general model for the salinization processes in the Mediterranean area, where the occurrence of evaporitic rocks in coastal aquifers is a common feature. In addition, due to intensive human activities and recent climatic changes, the Nurra has become vulnerable to desertification and, similarly to other Mediterranean islands, surface-water resources can periodically suffer from drastic shortage. With this in mind we report new data, regarding brackish waters of Na-Cl type of the Nurra, including major ions and selected trace elements (B, Br, I and Sr) and isotopic data, including δ18O, δD in water, and δ34S and δ18O in dissolved sulphate. To better depict the origin of the salinity we also analyzed a set of Nurra Triassic evaporites for mineralogical and isotopic composition. The brackish waters have Cl contents up to 2025 mg L-1 and the ratios between dissolved ions and chlorine, with the exception of the Br/Cl ratio, are not those expected on the basis of a simple mixing between rain water and seawater. The δ18O and δD data indicate that most of the waters are within the Regional Meteoric Water Line and the Global Meteoric Water Line supporting the idea that they are meteoric in origin. A relevant consequence of the

Calculation of isotope selective excitation of uranium isotopes using spectral simulation method

International Nuclear Information System (INIS)

Al-Hassanieh, O.

2009-06-01

Isotope ratio enhancement factor and isotope selectivity of 235 U in five excitation schemes (I: 0→10069 cm - 1 →IP, II: 0 →10081 cm - 1 →IP, III: 0 →25349 cm - 1→ IP, IV: 0→28650 cm - 1 →IP, V: 0→16900 cm - 1 →34659 cm - 1 →IP), were computed by a spectral simulation approach. The effect of laser bandwidth and Doppler width on the isotope ratio enhancement factor and isotope selectivity of 235 U has been studied. The photoionization scheme V gives the highest isotope ratio enhancement factor. The main factors which effect the separation possibility are the isotope shift and the relative intensity of the transitions between hyperfine levels. The isotope ratio enhancement factor decreases exponentially by increasing the Doppler width and the laser bandwidth, where the effect of Doppler width is much greater than the effect of the laser bandwidth. (author)

Geochemical characteristics of Tertiary saline lacustrine oils in the Western Qaidam Basin, northwest China

International Nuclear Information System (INIS)

Zhu Yangming; Weng Huanxin; Su Aiguo; Liang Digang; Peng Dehua

2005-01-01

Based on the systematic analyses of light hydrocarbon, saturate, aromatic fractions and C isotopes of over 40 oil samples along with related Tertiary source rocks collected from the western Qaidam basin, the geochemical characteristics of the Tertiary saline lacustrine oils in this region was investigated. The oils are characterized by bimodal n-alkane distributions with odd-to-even (C 11 -C 17 ) and even-to-odd (C 18 -C 28 ) predominance, low Pr/Ph (mostly lower than 0.6), high concentration of gammacerane, C 35 hopane and methylated MTTCs, reflecting the high salinity and anoxic setting typical of a saline lacustrine depositional environment. Mango's K 1 values in the saline oils are highly variable (0.99-1.63), and could be associated with the facies-dependent parameters such as Pr/Ph and gammacerane indexes. Compared with other Tertiary oils, the studied Tertiary saline oils are marked by enhanced C 28 sterane abundance (30% or more of C 27 -C 29 homologues), possibly derived from halophilic algae. It is noted that the geochemical parameters of the oils in various oilfields exhibit regular spatial changes, which are consistent with the depositional phase variations of the source rocks. The oils have uncommon heavy C isotopic ratios (-24%o to -26%o) and a flat shape of the individual n-alkane isotope profile, and show isotopic characteristics similar to marine organic matter. The appearance of oleanane and high 24/(24 + 27)-norcholestane ratios (0.57-0.87) in the saline oils and source rocks confirm a Tertiary organic source

Salinization and Saline Environments

Science.gov (United States)

Vengosh, A.

2003-12-01

, such as treated wastewater and agricultural drainage water. Two anthropogenic salinization cycles are introduced - the agricultural and the domestic cycles. Some useful geochemical fingerprinting tracers are also included for defining the sources of salinity. Finally, the chemical composition of future water resources is predicted, based on the chemical and isotopic fractionation associated with remediation and desalination.

An integrated hydrogeochemical and isotopic approach to study groundwater Salinization in the overexploited aquifers of Indo-Gangetic Plain, a part of NCR Delhi

Science.gov (United States)

Kumari, R.

2017-12-01

roundwater resources in arid and semi-arid areas are highly vulnerable to salinity problems. Inadequate availability of surface water supply, vagaries of mansoonal rainfall and overexploitation due to population pressure and rapid landuse change induced decline in groundwater levels and salinization has been observed in many Asian cities. After green revolution, large part of Indo-Gangetic plain groundwater salinization has been reported. One such region is National Capital Region, Delhi- India's largest and the world's second largest agglomeration of people and economic hub of Northern India. The present study includes National capital territory, Delhi, Gurgaon and Faridabad. In the present study, different graphical plots, Piper plot, saturation index values (using PHREEQC), stable isotopes (δ18O and δD) and GIS is used to create the database for analysis of spatial variation in respective water quality parameters as well as to decipher the hydrogeochemical process occurring in the area. Major ions are analysed to describe the composition and distribution of salinization and dissolution/precipitation dynamics. It was observed that groundwater weathering is governed by carbonate and silicate weathering and reverse ion-exchange, however due to semi-arid climate evaporation is also playing a major role in groundwater chemistry and salinity of the area. δ18O and δD regression line of groundwater samples of the study area is below the LMWL also suggest from non-equilibrium fractionation during evaporation. Large lateral variation in chloride concentration indicates impact of evapotranspiration rate during recharge. Most of water facies are of Na-Cl. Stable isotope (δ18O and δD) analysis helps to identify evaporation and to better understand recharge processes and mixing dynamics in the study region. Limited availability of surface water supply, no pricing exists for groundwater extraction has resulted in a widespread decline in the water table and intermixing of

Submarine Ground Water Discharge and Fate Along the Coast of Kaloko-Honokohau National Historical Park, Hawai'i:Part 2, Spatial and Temporal Variations in Salinity, Radium-Isotope Activity, and Nutrient Concentrations in Coastal Waters, December 2003-April 2006

Science.gov (United States)

Knee, Karen; Street, Joseph; Grossman, Eric E.; Paytan, Adina

2008-01-01

The aquatic resources of Kaloko-Honokohau National Historical Park, including rocky shoreline, fishponds, and anchialine pools, provide habitat to numerous plant and animal species and offer recreational opportunities to local residents and tourists. A considerable amount of submarine groundwater discharge was known to occur in the park, and this discharge was suspected to influence the park's water quality. Thus, the goal of this study was to characterize spatial and temporal variations in the quality and quantity of groundwater discharge in the park. Samples were collected in December 2003, November 2005, and April 2006 from the coastal ocean, beach pits, three park observation wells, anchialine pools, fishponds, and Honokohau Harbor. The activities of two Ra isotopes commonly used as natural ground-water tracers (223Ra and 224Ra), salinity, and nutrient concentrations were measured. Fresh ground water composed a significant proportion (8-47 volume percent) of coastal-ocean water. This percentage varied widely between study sites, indicating significant spatial variation in submarine groundwater discharge at small (meter to kilometer) scales. Nitrate + nitrite, phosphate, and silica concentrations were significantly higher in nearshore coastal-ocean samples relative to samples collected 1 km or more offshore, and linear regression showed that most of this difference was due to fresh ground-water discharge. High-Ra-isotope-activity, higher-salinity springs were a secondary source of nutrients, particularly phosphate, at Honokohau Harbor and Aiopio Fishtrap. Salinity, Ra-isotope activity, and nutrient concentrations appeared to vary in response to the daily tidal cycle, although little seasonal variation was observed, indicating that submarine ground-water discharge may buffer the park's water quality against the severe seasonal changes that would occur in a system where freshwater inputs were dominated by rivers and runoff. Ra-isotope-activity ratios indicated

Tracing groundwater salinization processes in coastal aquifers: a hydrogeochemical and isotopic approach in the Na-Cl brackish waters of northwestern Sardinia, Italy

Directory of Open Access Journals (Sweden)

G. Mongelli

2013-07-01

Full Text Available Throughout the Mediterranean, salinization threatens water quality, especially in coastal areas. This salinization is the result of concomitant processes related to both seawater intrusion and water–rock interaction, which in some cases are virtually indistinguishable. In the Nurra region of northwestern Sardinia, recent salinization related to marine water intrusion has been caused by aquifer exploitation. However, the geology of this region records a long history from the Palaeozoic to the Quaternary, and is structurally complex and comprises a wide variety of lithologies, including Triassic evaporites. Determining the origin of the saline component of the Jurassic and Triassic aquifers in the Nurra region may provide a useful and more general model for salinization processes in the Mediterranean area, where the occurrence of evaporitic rocks in coastal aquifers is a common feature. In addition, due to intensive human activity and recent climatic change, the Nurra has become vulnerable to desertification and, in common with other Mediterranean islands, surface water resources periodically suffer from severe shortages. With this in mind, we report new data regarding brackish and surface waters (outcrop and lake samples of the Na-Cl type from the Nurra region, including major ions and selected trace elements (B, Br, I, and Sr, in addition to isotopic data including δ18O, δD in water, and δ34S and δ18O in dissolved SO4. To identify the origin of the salinity more precisely, we also analysed the mineralogical and isotopic composition of Triassic evaporites. The brackish waters have Cl contents of up to 2025 mg L−1 , and the ratios between dissolved ions and Cl, with the exception of the Br / Cl ratio, are not those expected on the basis of simple mixing between rainwater and seawater. The δ18O and δD data indicate that most of the waters fall between the regional meteoric water line and the global meteoric water line, supporting the

Tracing groundwater salinization processes in coastal aquifers: a hydrogeochemical and isotopic approach in the Na-Cl brackish waters of northwestern Sardinia, Italy

Science.gov (United States)

Mongelli, G.; Monni, S.; Oggiano, G.; Paternoster, M.; Sinisi, R.

2013-07-01

Throughout the Mediterranean, salinization threatens water quality, especially in coastal areas. This salinization is the result of concomitant processes related to both seawater intrusion and water-rock interaction, which in some cases are virtually indistinguishable. In the Nurra region of northwestern Sardinia, recent salinization related to marine water intrusion has been caused by aquifer exploitation. However, the geology of this region records a long history from the Palaeozoic to the Quaternary, and is structurally complex and comprises a wide variety of lithologies, including Triassic evaporites. Determining the origin of the saline component of the Jurassic and Triassic aquifers in the Nurra region may provide a useful and more general model for salinization processes in the Mediterranean area, where the occurrence of evaporitic rocks in coastal aquifers is a common feature. In addition, due to intensive human activity and recent climatic change, the Nurra has become vulnerable to desertification and, in common with other Mediterranean islands, surface water resources periodically suffer from severe shortages. With this in mind, we report new data regarding brackish and surface waters (outcrop and lake samples) of the Na-Cl type from the Nurra region, including major ions and selected trace elements (B, Br, I, and Sr), in addition to isotopic data including δ18O, δD in water, and δ34S and δ18O in dissolved SO4. To identify the origin of the salinity more precisely, we also analysed the mineralogical and isotopic composition of Triassic evaporites. The brackish waters have Cl contents of up to 2025 mg L-1 , and the ratios between dissolved ions and Cl, with the exception of the Br / Cl ratio, are not those expected on the basis of simple mixing between rainwater and seawater. The δ18O and δD data indicate that most of the waters fall between the regional meteoric water line and the global meteoric water line, supporting the conclusion that they are

Microscopic calculation of parameters of the sdg interacting boson model for 104-110Pd isotopes

International Nuclear Information System (INIS)

Liu Yong

1995-01-01

The parameters of the sdg interacting boson model Hamiltonian are calculated for the 104-110 Pd isotopes. The calculations utilize the microscopic procedure based on the Dyson boson mapping proposed by Yang-Liu-Qi and extended to include the g boson effects. The calculated parameters reproduce those values from the phenomenological fits. The resulting spectra are compared with the experimental spectra

Four years of experience with the use of calculated isotopic correlations in establishing input balances at the La Hague plant

International Nuclear Information System (INIS)

Aries, M.; Patigny, P.; Bouchard, J.; Giacometti, A.; Girieud, R.

1983-01-01

For more than four years the La Hague reprocessing plant has been using calculated isotopic correlations to establish and check its input balances. The masses of uranium and plutonium entering the plant are determined by the gravimetric balance method, which utilizes the burnup obtained by calculated isotopic correlation as well as the Pu/U ratio measured at the dissolver after cross-checking with the values obtained by correlation. Further, a verification of all the parameters needed to establish these balances - whether physical or chemical in origin - is carried out systematically by means of internal coherence constants which make it possible to detect any anomalies in the dissolution data. The calculated isotopic correlations were evaluated when the analyses of numerous representative samples of irradiated fuel and experimental results of separated isotopic irradiation in water reactor spectra had been interpreted. The accuracy achieved was improved by allowing in the neutron calculations for effects inherent in the first reactor core and by selecting a set of calculation functions which attenuates (by compensation effects) the various perturbations in the irradiation history. The results obtained at La Hague with calculated isotopic correlations on nearly 600 t of reprocessed UO 2 , because of their large number and above all their high quality, suggest that it be proposed extending the method to other reprocessing plants. This could be done by the operator himself or by national or international control bodies within the framework of a safeguards arrangement. (author)

Evidence of a connection between the Atlantic and Mediterranean during the Messinian Salinity Crisis from Pb and Nd isotopes

Science.gov (United States)

Modestou, Sevasti; Gutjahr, Marcus; Fietzke, Jan; Rodés, Ángel; Frank, Martin; Bolhão Muiños, Susana; Ellam, Rob; Flecker, Rachel

2014-05-01

Prior to the opening of the Gibraltar Strait at 5.33 Ma, the Betic (southern Spain) and Rifian (northern Morocco) marine palaeocorridors linked the Mediterranean to the Atlantic. Although the central regions of these corridors have been heavily eroded due to uplift, evidence published to date indicates that both closed before the onset of the Messinian Salinity Crisis (MSC; 5.97 to 5.33 Ma [1, 2]). However, pre-MSC corridor closure presents a paradox, as the volume of halite deposited within the Mediterranean basin requires several times the volume of seawater contained in the basin itself. In this regard, radiogenic isotopes such as Sr, Pb, and Nd can provide key information about the timing of exchange through the Betic and Rifian palaeogateways. Due to the resolvable isotopic difference in Nd isotope signatures of outgoing Mediterranean and incoming Atlantic water masses, demonstrated both for the present day as well as the past environment, this isotope system can be used to identify exchange between these two water bodies. Although less well constrained to date, the Pb isotope system can be used in a similar manner due to its short residence time in seawater and interbasin variability. A high resolution Pb isotope record extracted using laser ablation from ferromanganese crust 3514-6 (recovered from the Lion Seamount, NE Atlantic, water depth 690-940 m) indicates a relatively constant Pb isotope signature before, during and after the MSC period. The previously published [3] Nd isotope record of crust 3514-6 corroborates that the crust was deposited in a current distinct from NE Atlantic Deep water or Antarctic Intermediate Water, the principal currents in the region of the Lion Seamount. The combined Pb and Nd isotope evolution suggests that Mediterranean Outflow Water (MOW) was continuously advected into the NE Atlantic during and after the MSC. Furthermore, preliminary Nd isotope records from Late Miocene sediments collected in the Sorbas Basin, Spain

Efigie: a computer program for calculating end-isotope accumulation by neutron irradiation and radioactive decay

International Nuclear Information System (INIS)

Ropero, M.

1978-01-01

Efigie is a program written in Fortran V which can calculate the concentration of radionuclides produced by neutron irradiation of a target made of either a single isotope or several isotopes. The program includes optimization criteria that can be applied when the goal is the production of a single nuclide. The effect of a cooling time before chemical processing of the target is also accounted for.(author) [es

N2-fixation in fababean (vicia faba l.) grown in saline and non saline conditions using 15N tracer technique

International Nuclear Information System (INIS)

Khalifa, Kh.; Kurdali, F.

2002-09-01

A pot experiment was conducted to study the performance of growing fababean and barley under saline conditions, in terms of, dry matter yield, total nitrogen and, percentages and amount of N derived from soil, fertilizer and atmosphere using 15 N isotope dilution method. Three saline treatments were performed: First, plants were grown in saline soil and irrigated with saline water (Ws Ss), Second, Plants were grown in saline soil and irrigated with saline water (Ws Ss); and Third, Plants grown in non saline soil and irrigated with saline water (Ws Sn). Furthermore, a control treatment was performed by using non-saline soil and non-saline water (Wn Sn). The different salinity treatments reduced plant growth and the reduction was more pronounced in fababean than in barley. However, under conditions of either saline soil-soft irrigation water or non saline soil-salty irrigation water, the relative growth reduction did not exceed 50% of the control; whereas, a significant negative effect was obtained when plants were grown under completely saline conditions of both soil and irrigation water. Percentage of N 2 -fixed (% Ndfa) was not negatively affected by saline conditions. However, our results clearly demonstrated that the effect of salinity in fababean was more evident on plant growth than on N 2 -fixing activity. Further studies are needed to obtain more salt tolerant faba bean genotypes in terms of growth and yield. This could be simultaneously improve yield and N 2 -fixation under sever saline conditions. (author)

Productive use of saline lands

International Nuclear Information System (INIS)

2003-01-01

Water is essential for life, and not least for agricultural activity. It interacts with solar energy to determine the climate of the globe, and its interaction with carbon dioxide inside a plant results in photosynthesis on which depends survival of all life. Much of the water available to man is used for agriculture and yet its usage has not been well managed. One result has been the build up of soil salinity. The Department of Technical Co-operation is sponsoring a programme, with technical support from the Department of Research and Isotopes, to make more productive use of salt-affected land and to limit future build up of salinity. (IAEA)

Environmental isotopes investigation in groundwater of Challaghatta ...

African Journals Online (AJOL)

Administrator

Radiogenic isotopes (3H and 14C) and stable isotope (18O) together with TDS, EC and salinity of water were used to ..... Tritium (3H). Relative dating of groundwater has been carried ... that falls to Earth has small amounts of tritium. During the.

A on-line method for the determination of lead and lead isotope ratios in fresh and saline waters by inductively coupled plasma mass spectrometry

International Nuclear Information System (INIS)

Halicz, Ludwik; Lam, J.W.H.; McLaren, J.W.

1994-01-01

A previously reported on-line ICP-MS method for the determination of lead and other trace elements in seawater has been re-examined to determine its suitability for the determination of lead isotope ratios ( 206 Pb/ 207 Pb and 207 Pb/ 208 Pb) in fresh and saline natural waters. A detection limit of 0.9 ng/1 for total lead (for a 5 ml sample) was achieved. Precision of isotope ratio data was 0.2-0.3% RSD at a Pb concentration of 1 μg/l, and was still better than 2% at concentrations of only 10-40 ng/1 in seawater certified reference materials (CRMs). For all three natural water CRMs examined, measured precision was very close to the limit predicted by counting statistics. (Author)

Microscopic calculation of the Majorana parameters of the interacting boson model for the Hg isotopes

Energy Technology Data Exchange (ETDEWEB)

Druce, C.H.; Barrett, B.R. (Arizona Univ., Tucson (USA). Dept. of Physics); Pittel, S. (Delaware Univ., Newark (USA). Bartol Research Foundation); Duval, P.D. (BEERS Associates, Reston, VA (USA))

1985-07-11

The parameters of the Majorana interaction of the neutron-proton interacting boson model are calculated for the Hg isotopes. The calculations utilize the Otsuka-Arima-Iachello mapping procedure and also lead to predictions for the other boson parameters. The resulting spectra are compared with experimental spectra and those obtained from phenomenological fits.

Microscopic calculation of the Majorana parameters of the interacting boson model for the Hg isotopes

Science.gov (United States)

Druce, C. H.; Pittel, S.; Barrett, B. R.; Duval, P. D.

1985-07-01

The parameters of the Majorana interaction of the neutron-proton interacting boson model are calculated for the Hg isotopes. The calculations utilize the Otsuka-Arima-Iachello mapping procedure and also lead to predictions for the other boson parameters. The resulting spectra are compared with experimental spectra and those obtained from phenomenological fits.

Temperature and void reactivity coefficient calculations for the high flux isotope reactor safety analysis report

International Nuclear Information System (INIS)

Engle, W.W. Jr.; Williams, L.R.

1994-07-01

This report provides documentation of a series of calculations performed in 1991 in order to provide input for the High Flux Isotope Reactor Safety Analysis Report. In particular, temperature and void reactivity coefficients were calculated for beginning-of-life, end-of-life, and xenon equilibrium (29 h) conditions. Much of the data used to prepare the computer models for these calculations was derived from the original HFIR nuclear design study

A calculation of the surface recombination rate constant for hydrogen isotopes on metals

International Nuclear Information System (INIS)

Baskes, M.J.

1980-01-01

The surface recombination rate constant for hydrogen isotopes on a metal has been calculated using a simple model whose parameters may be determined by direct experimental measurements. Using the experimental values for hydrogen diffusivity, solubility, and sticking coefficient at zero surface coverage a reasonable prediction of the surface recombination constant may be made. The calculated recombination constant is in excellent agreement with experiment for bcc iron. A heuristic argument is developed which, along with the rate constant calculation, shows that surface recombination is important in those metals in which hydrogen has an exothermic heat of solution. (orig.)

Calculation and mitigation of isotopic interferences in liquid chromatography-mass spectrometry/mass spectrometry assays and its application in supporting microdose absolute bioavailability studies.

Science.gov (United States)

Gu, Huidong; Wang, Jian; Aubry, Anne-Françoise; Jiang, Hao; Zeng, Jianing; Easter, John; Wang, Jun-sheng; Dockens, Randy; Bifano, Marc; Burrell, Richard; Arnold, Mark E

2012-06-05

A methodology for the accurate calculation and mitigation of isotopic interferences in liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) assays and its application in supporting microdose absolute bioavailability studies are reported for the first time. For simplicity, this calculation methodology and the strategy to minimize the isotopic interference are demonstrated using a simple molecule entity, then applied to actual development drugs. The exact isotopic interferences calculated with this methodology were often much less than the traditionally used, overestimated isotopic interferences simply based on the molecular isotope abundance. One application of the methodology is the selection of a stable isotopically labeled internal standard (SIL-IS) for an LC-MS/MS bioanalytical assay. The second application is the selection of an SIL analogue for use in intravenous (i.v.) microdosing for the determination of absolute bioavailability. In the case of microdosing, the traditional approach of calculating isotopic interferences can result in selecting a labeling scheme that overlabels the i.v.-dosed drug or leads to incorrect conclusions on the feasibility of using an SIL drug and analysis by LC-MS/MS. The methodology presented here can guide the synthesis by accurately calculating the isotopic interferences when labeling at different positions, using different selective reaction monitoring (SRM) transitions or adding more labeling positions. This methodology has been successfully applied to the selection of the labeled i.v.-dosed drugs for use in two microdose absolute bioavailability studies, before initiating the chemical synthesis. With this methodology, significant time and cost saving can be achieved in supporting microdose absolute bioavailability studies with stable labeled drugs.

Connection factor calculation for isotopic neutron flux measurements with foil detectors

International Nuclear Information System (INIS)

Avila L, J.

1987-01-01

Thermal and resonance neutron self-shielding factors, neutron flux distortion and edge effects as well as a connection factor for neutron flux profile around a foil detector have been calculated. A general expression for resonance self shielding factor is presented in order to take into account the most important resonances for a given isotope. A computer program SPRESYTER.BAS was written and results for In-115 and Au-197 foils are given

Sulfur isotopic study of sulfate in the aquifer of Costa de Hermosillo (Sonora, Mexico) in relation to upward intrusion of saline groundwater, irrigation pumping and land cultivation

International Nuclear Information System (INIS)

Szynkiewicz, Anna; Medina, Miguel Rangel; Modelska, Magdalena; Monreal, Rogelio; Pratt, Lisa M.

2008-01-01

Groundwater from the Costa de Hermosillo aquifer has been used extensively for irrigation over the past 60 a in the Sonora region of northwestern Mexico resulting in salinization of fresh groundwater resources. Salinization of groundwater is most pronounced on the western/coastal side of the aquifer, with an aerial extent of 26.7 km 2 , where maximum values are reported for conductivity (31 mS/cm) and Cl - concentrations (16,271 mg/L). Salinization is likely to increase if groundwater pumping continues at levels comparable to the present time. Upward incursion of marine water into the aquifer is inferred from δ 2 H (-7.2 per mille ) and δ 18 O (+1.6 per mille ) compositions of groundwater samples with the highest conductivity. Compared to modern seawater in the Gulf of California, ratios of SO 4 /Cl and Cl/Br are small (0.01 and 33, respectively) and the S isotopic composition of SO 4 2- is high (+32.7%) in the most saline portions of the Costa de Hermosillo. This saline groundwater is inferred to result from an earlier phase of dissimilatory bacterial SO 4 2- reduction coupled to decomposition of organic matter in marine blue clays deposited during the Miocene/Pliocene transgression. The isotopic composition of present-day surface discharge from agricultural fields is substantially enriched in 32 S due to widespread application of (NH 4 ) 2 SO 4 fertilizers and potential mobilization of S from mineral resources. Surface water discharging from irrigated fields has δ 34 S values ranging from -2.1 to 3.3 per mille which are distinctly different from groundwater and surface water in adjacent non-agricultural areas with δ 34 S values ranging from 5.2 to 13.5 per mille . Prolonged irrigation pumping that promotes the incursion of air to the subsurface could enhance the weathering of S-bearing minerals such as magmatic sulfides, producing 32 S-enriched SO 4 2-

Using the Wolfsberg--Schactschneider program to calculate equilibrium constants for isotopic acetylenes

International Nuclear Information System (INIS)

Liu, D.K.K.; Pyper, J.W.

1977-01-01

Equilibrium constants were calculated for the gas-phase isotopic exchange reactions C 2 H 2 + C 2 D 2 = 2C 2 HD and C 2 H 2 + D 2 O = C 2 D 2 + H 2 O at temperatures ranging from 40 to 2000 0 K. No corrections to the harmonic approximation were made. The results agree quite well with experimental measurements

Isotopic fractionation of NBS oxalic acid and its influence in the calculated age of materials

International Nuclear Information System (INIS)

Nehmi, V.A.

1979-10-01

The intensity of the isotopic fractionation during the oxidation of NBS oxalic acid to carbon dioxide was checked. 30 reactions of oxidation of NBS oxalic acid with potassium permanganate were made. The resultant isotopic composition of CO 2 has been determined with a mass-spectrometer. A conclusion has been reached that the average of Δ 13 C is - 18.9% o with variation between - 17.7 and - 21.2%o. For values of Δ 13 C equal to - 22.0%o, the calculated age with isotopic correction shows the following deviations in relation to non-corrected age: 4% for materials of 1,000 years and 0.3% for 20,000 years.(Author) [pt

Application of the isotopic index in isotope geochemical investigation

International Nuclear Information System (INIS)

Schuetze, H.

1982-06-01

A method is described which allows to calculate approximately isotope exchange equilibria between different crystalline silicates. The algorithm uses a newly introduced isotopic index. It is defined using isotopic increments of the variant types of silicatic bonds. This isotopic index gives a quantitative measure of the ability to enrich 18 O or 30 Si, respectively. The dependence of isotopic fractionations on temperature can be calculated approximately by means of the isotopic index, too. On this theoretical base some problems of magmatism and two varieties of an isotope geochemical model of the evolution of the Earth's crust are treated. Finally, the possibility is demonstrated to give prognostic statements about the likelihood of ore bearing of different granites. (author)

Isotopic characteristics of shells Mytilus galloprovincialis from eastern coastal area of Adriatic Sea

Directory of Open Access Journals (Sweden)

Tjaša Kanduč

2006-06-01

Full Text Available Samples of Mytilus galloprovincialis were collected from entire Eastern Adriatic coast to determine δ18O and δ13C performed on calcite and aragonite shell layers. The aim of this work was to check whether shells of M. galloprovincialis are good environmental indicators (water temperature, salinity. Based on measured isotopic composition of oxygen in shell layers and assumed isotopic composition in water temperatures of calcite and aragonite of shell layers were calculated. The calculated temperatures for M. galloprovincialis shell growth of calcite and aragonite shell layer are in good agreement with measured temperatures of sea water. According to our results of δ18O and δ13C in shell layers we canseparate the locations of the investigated area into three groups: those with more influence of fresh water, those with less influence of fresh water and those of marine environments.

Report on the consultants meeting on identification of crop species/cultivars for drought and salinity tolerance for sustained crop yields by using nuclear techniques, in particular the carbon isotope discrimination

International Nuclear Information System (INIS)

2001-01-01

A Consultants Meeting on Identification of Crop Species/Cultivars for Drought and Salinity Tolerance for Sustained Crop Yields by Using Nuclear Techniques, in Particular the Carbon Isotope Discrimination. was held in Vienna at the IAEA Headquarters from 12-16 November 2001. This meeting was conducted in conjunction with a Group Meeting on Novel Approaches for Improving Crop Tolerance to Salinity and Drought. Five consultants from Australia, Mexico, Pakistan, UK and the USA and one representative from FAO attended the Consultant Meeting and nine participants from Australia, Canada, China, Germany, India, Israel, Pakistan, South Africa and the USA attended the Group Meeting. First two days of the meeting consisted of five technical sessions during which the participants presented papers on various approaches for improving crop tolerance to salinity and drought and the role of nuclear techniques in identification of plants tolerant to the above abiotic stresses. After the presentations, two working groups were formed: one consisting of the participants of the Consultants Meeting and the other the participants of the Group Meeting. The consultants proposed various strategies for using the carbon isotope discrimination technique as a selection tool for identifying higher yielding crop genotypes especially in wheat and rice cropping systems under drought and saline conditions. A proposal was formulated to address the above issues in a framework of a CRP. The participants of the Group Meeting reviewed conventional and molecular approaches for improving crop tolerance to salinity and drought and research priorities were identified for future work on crop productivity improvement under the above stress factors. Recommendations of both working groups were presented at the final session of the meeting. This report provides the details of the proposal formulated by the consultants. Refs

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

The origin of brackish and saline groundwater in the coastal area of the Netherlands

NARCIS (Netherlands)

Post, VEA; Van der Plicht, H; Meijer, HAJ

An explanation is presented for the origin of brackish to saline groundwater in the coastal area of the Netherlands based on geological, chemical (chlorinity), isotopic and geophysical data. A critical review of all possible salinization mechanisms shows that the origin of the brackish water is

Stable oxygen and hydrogen isotopes of brines - comparing isotope ratio mass spectrometry and isotope ratio infrared spectroscopy

Science.gov (United States)

Ahrens, Christian; Koeniger, Paul; van Geldern, Robert; Stadler, Susanne

2013-04-01

Today's standard analytical methods for high precision stable isotope analysis of fluids are gas-water equilibration and high temperature pyrolysis coupled to isotope ratio mass spectrometers (IRMS). In recent years, relatively new laser-based analytical instruments entered the market that are said to allow high isotope precision data on nearly every media. This optical technique is referred to as isotope ratio infrared spectroscopy (IRIS). The objective of this study is to evaluate the capability of this new instrument type for highly saline solutions and a comparison of the analytical results with traditional IRMS analysis. It has been shown for the equilibration method that the presence of salts influences the measured isotope values depending on the salt concentration (see Lécuyer et al, 2009; Martineau, 2012). This so-called 'isotope salt effect' depends on the salt type and salt concentration. These factors change the activity in the fluid and therefore shift the isotope ratios measured by the equilibration method. Consequently, correction factors have to be applied to these analytical data. Direct conversion techniques like pyrolysis or the new laser instruments allow the measurement of the water molecule from the sample directly and should therefore not suffer from the salt effect, i.e. no corrections of raw values are necessary. However, due to high salt concentrations this might cause technical problems with the analytical hardware and may require labor-intensive sample preparation (e.g. vacuum distillation). This study evaluates the salt isotope effect for the IRMS equilibration technique (Thermo Gasbench II coupled to Delta Plus XP) and the laser-based IRIS instruments with liquid injection (Picarro L2120-i). Synthetic salt solutions (NaCl, KCl, CaCl2, MgCl2, MgSO4, CaSO4) and natural brines collected from the Stassfurt Salt Anticline (Germany; Stadler et al., 2012) were analysed with both techniques. Salt concentrations ranged from seawater salinity

Isotope hydrology of ground waters of the Kalahari, Gordonia

International Nuclear Information System (INIS)

Verhagen, B.Th.

1985-01-01

Environmental isotope observations were conducted on ground waters from approximately 50 boreholes covering a substantial part of Gordonia. The quality of these waters ranges from fresh to saline. The observed isotope ratios cover a wide range of values, indicating varied hydrological conditions. The most important conclusions arrived at by this study are: 1. no important regional movement of ground water occurs at present; 2. there is widespread evidence of diffuse rainfall recharge; and 3. an important part of ground-water salinity is derived from the unsaturated zone, during such recharge

Isotope anomalies in oxygen isotope exchange equilibrium systems

International Nuclear Information System (INIS)

Kotaka, M.

1997-01-01

The purpose of the present work is to elucidate the isotope anomalies in oxygen isotope exchange equilibrium systems, according to the calculations of the equilibrium constants for oxygen isotopic exchange reactions, and the calculations of the oxygen isotope separation factors between two phases. The equilibrium constants (K65, K67, K68 and K69) of 16 O- 15 O, 16 O 17 O, 16 O- 18 O, and 16 O- 19 O exchange reactions between diatomic oxides were calculated in a wide temperature range on the basis of quantum statistical mechanics. Many equilibrium constants showed the anomalous mass effects, and then had the crossover temperatures and the mass independent fractionation (MIF) temperatures which held K67 = K65, K67 = K68, or K67 = K69, etc. For example, the equilibrium constants for the reactions between OH and the other diatomic oxides (MO) showed the anomalous mass effects, when M was Li, Na, Mg, K, Fe, Al, Ge, Zr, Pt, etc. The 16 O 15 O, 16 O 17 O, 16 O- 18 O, and 16 O- 19 O oxygen isotope separation factors (S65, S67, S68 and S69) between two phases were calculated, when OH and CO were in the first phase, and SiO was in the second phase. Although the oxygen isotopic exchange equilibria in the two phases had no MIF and crossover temperatures, the separation factors showed the anomalous mass effects and had the temperatures. According to what is called the normal mass effects for the equilibrium constant of isotopic exchange reaction, the value of InK68/InK67 is 1.885. Therefore, the value of InS68/InS67 should be 1.885 too. The value calculated, however, widely changed. It can be concluded from the results obtained in the present work that some oxygen isotopic exchange equilibria cause the anomalous mass effects, the anomalous oxygen isotope separation factors, and then isotope anomalies

Calculations of (n,2n) reaction cross sections for Barium isotopes from 5 to 20 MeV

Science.gov (United States)

Sahan, Halide; Sahan, Muhittin; Tel, Eyyup

2017-09-01

In this study, the excitation functions of (n,2n) reactions for 30,32,34,35,37,38Ba isotopes are calculated using TALYS 1.6, EMPIRE-3.2.2, and ALICE-GDH codes based on statistical model up to 20 MeV. Moreover, the cross section for each isotope have also been estimated at 14.2 MeV using semi empirical formula developed by four different authors. The calculated and estimated cross-sections are compared with experimental cross-sections from EXFOR and compared with the evaluation data in ENDF/B-VII.1 library. Results are close agreement with the experimental data from literature.

Diversity of sulfur isotope fractionations by sulfate-reducing prokaryotes

DEFF Research Database (Denmark)

Detmers, Jan; Brüchert, Volker; Habicht, K S

2001-01-01

Batch culture experiments were performed with 32 different sulfate-reducing prokaryotes to explore the diversity in sulfur isotope fractionation during dissimilatory sulfate reduction by pure cultures. The selected strains reflect the phylogenetic and physiologic diversity of presently known...... sulfate reducers and cover a broad range of natural marine and freshwater habitats. Experimental conditions were designed to achieve optimum growth conditions with respect to electron donors, salinity, temperature, and pH. Under these optimized conditions, experimental fractionation factors ranged from 2.......0 to 42.0 per thousand. Salinity, incubation temperature, pH, and phylogeny had no systematic effect on the sulfur isotope fractionation. There was no correlation between isotope fractionation and sulfate reduction rate. The type of dissimilatory bisulfite reductase also had no effect on fractionation...

An Investigation into the Relationship Between Distillate Yield and Stable Isotope Fractionation

Science.gov (United States)

Sowers, T.; Wagner, A. J.

2016-12-01

Recent breakthroughs in laser spectrometry have allowed for faster, more efficient analyses of stable isotopic ratios in water samples. Commercially available instruments from Los Gatos Research and Picarro allow users to quickly analyze a wide range of samples, from seawater to groundwater, with accurate isotope ratios of D/H to within ± 0.2 ‰ and 18O/16O to within ± 0.03 ‰. While these instruments have increased the efficiency of stable isotope laboratories, they come with some major limitations, such as not being able to analyze hypersaline waters. The Los Gatos Research Liquid Water Isotope Analyzer (LWIA) can accurately and consistently measure the stable isotope ratios in waters with salinities ranging from 0 to 4 grams per liter (0 to 40 parts per thousand). In order to analyze water samples with salinities greater than 4 grams per liter, however, it was necessary to develop a consistent method through which to reduce salinity while causing as little fractionation as possible. Using a consistent distillation method, predictable fractionation of δ 18O and δ 2 H values was found to occur. This fractionation occurs according to a linear relationship with respect to the percent yield of the water in the sample. Using this method, samples with high salinity can be analyzed using laser spectrometry instruments, thereby enabling laboratories with Los Gatos or Picarro instruments to analyze those samples in house without having to dilute them using labor-intensive in-house standards or expensive premade standards.

Climate and isotopic tracers

International Nuclear Information System (INIS)

Jean-Baptiste, Ph.

1997-01-01

The applications of natural radioactivity and isotopic measurements in the sciences concerning Earth and its atmosphere, are numerous: carbon 14 dating with the Tandetron apparatus at the Cea, measurement of oxygen 18 in coral or sediment limestone for the determination of ocean temperature and salinity, carbon 14 dating of corals for the determination of sea level variations, deuterium content in polar ice-cap leads to temperature variations determination; isotopic measurements also enable the determination of present climate features such as global warming, oceanic general circulation

Evaluation of salt tolerance in wheat genotypes using growth and carbon isotopes discrimination technique

International Nuclear Information System (INIS)

Shirazi, M.U.; Khan, M.A.; Mujtaba, S.M.; Shereen, A.

2015-01-01

Studies were conducted in green house to select suitable salt tolerant wheat genotypes on the basis of growth performance and carbon isotopes discrimination (CID) technique. Nine newly developed double haploids (DH) wheat genotypes were tested under gravel culture, along with salt tolerant (LU-26s) and high yielding (Sarsabz) checks. The crop was irrigated by non-saline (control) and saline (12dS/m) water and raised up to maturity, growth parameters (i.e. plant height, plant biomass, productive tillers, spike length, number of spiklets/spike, number of grains / spike, grain weight/ spike and grain yield/ 15 plants) were recorded after harvesting. Plant samples (straw) were collected and were analyzed for carbon isotopic ratio (C12/ C13) from IAEA laboratories Vienna Austria. The data showed that there was significant decrease in all the growth parameters due to salinity. On the basis of performance in different growth parameters it was found that wheat genotypes V3-DH, V9-DH, V10-DH, V13-DH, and LU-26s had good response at 12dSm-1, thus can be categorized as better performing genotypes. Studies on carbon isotopes discrimination (CID) showed a decreasing trend under salinity. Mean CID values were 20.86 and 17.49 under two environments (non saline and saline, respectively), showing an overall 19% decrease under salinity. Generally the wheat genotypes having higher grain yield also had high carbon isotopes discrimination (CID). The relationship between grain yield and CID was positive (R2 = 0.695). The genotypes V10-DH, V13-DH with lower decrease in CID (i.e. 1.2 and 11.0%, respectively), also had high grain yield under salinity. Therefore the studies suggest that we can include CID technique as one of the selection criteria for salt tolerance. (author)

Quantum mechanical calculation of the adsorption of hydrogen isotopes on metallic nickel

International Nuclear Information System (INIS)

Zhu Zhenghe; Liu Youcheng; Wang Hongyan; Jiang Gang; Tan Mingliang

1998-01-01

The electronic ground state of NiH, NiD and NiT is derived to be 2 Σ + based on atomic and molecular reaction statics, then, energy E, heat capacity at constant volume C V and entropy S of these molecules have been calculated using QCISD/6-311G ** method. considering the characteristics of different motion types, the electronic and vibrational energy or entropy of molecule are assumed to be the corresponding values of their solid states. Then, it is easy to calculate ΔH degree, ΔS degree, ΔG degree and equilibrium pressure and examine the isotopic effect. The present method is somehow applicable to theoretical study on the storage-hydrogen materials

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

Energy Technology Data Exchange (ETDEWEB)

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

2001-08-01

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

Environmental isotope study of a groundwater supply project in the Kalahari of Gordonia

International Nuclear Information System (INIS)

Verhagen, B.T.

1984-01-01

A feasibility study for a central fresh groundwater supply scheme in the Kalahari of the Gordonia district, South Africa, provided the opportunity to study fresh and saline water occurrences in detail with environmental isotopes. The isotopic and chemical signals show a clear contrast among groundwaters below a river bed, an extended fresh groundwater body and saline groundwaters in close proximity to the river. Carbon-14, tritium and stable-isotope data lead to a vertical rain recharge model rather than a regional flow mechanism for an understanding of the various water occurrences, their interrelationships and varied hydrochemistry. (author)

Using a dual isotopic approach to trace sources and mixing of sulphate in Changjiang Estuary, China

International Nuclear Information System (INIS)

Li Siliang; Liu Congqiang; Patra, Sivaji; Wang Fushun; Wang Baoli; Yue Fujun

2011-01-01

Highlights: → Changjiang Estuary plays an important role in transportation of the water and solute. → The dual isotopic method could be used to understand sulfate biogeochemistry in estuaries. → Mixing processes should be a major factor involved in the distribution of water and sulphate. → Sulphate in the Changjiang River mainly derived from atmospheric deposition, evaporite dissolution and sulphide oxidation. - Abstract: The dual isotopic compositions of dissolved SO 4 2- in aquatic systems are commonly used to ascertain SO 4 2- sources and possible biogeochemical processes. In this study, the physical parameters, major anions and isotopic compositions of SO 4 2- in water samples from Changjiang River (Nanjin) to the East Sea in Changjiang Estuary were determined. The salinity ranged from 0 per mille to 32.3 per mille in the estuary water samples. The Cl - ,SO 4 2- concentrations and δ 18 O-H 2 O values followed the salinity variations from freshwater to seawater, which indicated that mixing processes might be a major factor involved in the distribution of water and solutes. The contents and isotopic compositions of SO 4 2- suggested that atmospheric deposition, evaporite dissolution and sulphide oxidation were the major sources of dissolved SO 4 2- in the freshwater of Changjiang River. In addition, the mixing model calculated by contents and isotopic compositions of SO 4 2- indicated that the mixing of freshwater and sea water was the major factor involved in SO 4 2- distribution in Changjiang Estuary. However, slightly elevated δ 18 O-SO 4 values were observed in the turbidity maximum zone, which suggested that biological processes might affect the O isotopic compositions of SO 4 2- there.

Measurement of N2 fixation in Sesbania aculeata pers. and Sorghum bicolor L. grown in intercropping system, under saline conditions, using 15N isotopic dilution technique

International Nuclear Information System (INIS)

Kurdali, F.; Khalifa, K.; Janat, M.

2001-09-01

A field experiment was conducted under saline conditions (soil EC e 15, water EC w 8 dS/m/m) to evaluate the performance of sole crops and inter crops of Sesbania aculeata and Sorghum bicolor (1:1 row ratio) in terms of dry matter production, total N yield, soil N uptake and N 2 -fixation using 15 N isotope dilution method. Dry matter yield in sole crop of sesbania was significantly higher that that of sole sorghum; whereas, that of the inter cropping was significantly lower than sole sesbania, but was similar to that produced by sole sorghum. Total nitrogen yield in sole sesbania was four-fold than that accumulated in sole sorghum, whereas, that of mixed cropping was 2.6 fold compared to that of sole sorghum. The LER of total N yield was higher than 1 reflecting a greater advantage of inter cropping system in terms of land use efficiency. The proportion of N derived from N 2 fixation (%Ndfa) in the sesbania was increased from 63 to 79%, for sole and inter cropping system, respectively. There was no evidence of a significant transfer of N from the sesbania to the sorghum. Results on the relative growth of plants on saline soil compared with non-saline soil clearly demonstrated that sesbania was more salt tolerant than the sorghum. soil nitrogen uptake by plants, particularly in sorghum, was adversely affected by salinity. However, amounts of N 2 fixed by sole sesbania grown is saline soil was close or even higher than on non-saline soil. The use of inter cropping systems of legumes and non-legumes could be a promising agricultural approach to reutilize wasted lands, after a careful selection of appropriate tolerant genotypes to prevailing saline conditions. (author)

Comparison of calculated and experimental values of the yields of xenon isotopes in reactions with high-energy protons

International Nuclear Information System (INIS)

Shukolyukov, A.Yu.; Katargin, N.V.; Baishev, I.S.

1989-01-01

Calculations of the cumulative yields of isotopes of Xe have been carried out on the basis of the semi-empirical formula of Silverberg and Tsao for Ba- and Dy-targets and bombarding proton energies in the range 100-1050 MeV. Results are compared with experimental data for the yields of Xe isotopes, and domains of applicability of the semi-empirical formula are determined

Hydrochemical and isotopic characterization of groundwater in the Ghis-Nekor plain (northern Morocco)

Science.gov (United States)

Chafouq, D.; El Mandour, A.; Elgettafi, M.; Himi, M.; Chouikri, I.; Casas, A.

2018-03-01

The coastal aquifer of Ghis-Nekor (Morocco) was studied to identify the major processes causing salinization of groundwater. In fact, a geochemical approach multi tracer (general chemistry and isotopes - δ2H, δ18O-H2O, δ34S, δ18O-SO4) was utilized, with the hydrodynamics to explain the processes responsible for the salinization of groundwater, and for identttifying areas most vulnerable to seawater intrusion. The recharge of the aquifer is mainly by the Al-Khattabi dam, the Nekor River and the Ghis River, on the eastern border of the plain. The water that feeds the aquifer shows a relatively high level of salinity and for this reason, the majority of sampled wells indicate high values of electric conductivity and total salinity which arrives at 7.5 g L-1. The plot of the geochemical results analyzes of groundwater in the Piper diagram shows two distinct chemical facies; sodium chloride-facies and chlorinated calcium and magnesium sulfated facies. The concentrations of 18O range between -4.15‰ and -5.73‰, while the values of 2H range between -28.4‰ and -41.7‰. The Nekor river water is depleted in heavy isotopes, and the isotopic compositions are in the order on -6‰ for 18O and -40.5‰ for deuterium. Most of the wells have a slope <8 indicating a slight evaporation before infiltration. The data show low and variable d-excess values (range from -0.02‰ to 11.6‰), reflect recharge during different climatic conditions. The isotopic concentrations of 18O-SO4 vary between 4.35‰ and 8.60‰, while the 34S isotope values range from -4.3‰ to 9.9‰. For Ghis River, these values are between -4.4‰ and 4.95‰, respectively, for sulfur and oxygen. The interpretation of the chemical and isotopic results suggesting the intrusion of seawater to increase salinity of groundwater in the region is low. However, only the NE area shows probable contamination of seawater. In contrast, wells are saline independent of seawater intrusion, the origin of the high

Salinization of porewater in a multiple aquitard-aquifer system in Jiangsu coastal plain, China

Science.gov (United States)

Li, Jing; Liang, Xing; Zhang, Yanian; Liu, Yan; Chen, Naijia; Abubakari, Alhassan; Jin, Menggui

2017-12-01

Chemical and isotopic compositions were analyzed in porewater squeezed from a clayey aquitard in Jiangsu coastal plain, eastern China, to interpret the salinity origin, chemical evolution and water-mass mixing process. A strong geochemical fingerprint was obtained with an aligned Cl/Br ratio of 154 in the salinized aquitard porewater over a wide Cl- concentration range (396-9,720 mg/L), indicating that porewater salinity is likely derived from a mixing with old brine with a proportion of less than 20%. Very small contributions of brine exerted limited effects on water stable isotopes. The relationships between porewater δ18O and δD indicate that shallow and intermediate porewaters could be original seawater and were subsequently diluted with modern meteoric water, whereas deep porewaters with depleted stable isotopic values were probably recharged during a cooler period and modified by evaporation and seawater infiltration. The cation-Cl relationship and mineralogy of associated strata indicate that porewater has been chemically modified by silicate weathering and ion-exchange reactions. 87Sr/86Sr ratios of 0.7094-0.7112 further confirm the input source of silicate minerals. Numerical simulations were used to evaluate the long-term salinity evolution of the deep porewater. The alternations of boundary conditions (i.e., the third aquifer mixed with brine at approximately 70 ka BP, followed by recharge of glacial meltwater at 20-25 ka BP, and then mixing with Holocene seawater at 7-10 ka BP) are responsible for the shift in porewater salinity. These timeframes correspond with the results of previous studies on ancient marine transgression-regression in Jiangsu coastal plain.

Influence of temperature and salinity on hydrodynamic forces

Directory of Open Access Journals (Sweden)

A. Escobar

2016-12-01

Full Text Available The purpose of this study is to introduce an innovative approach to offshore engineering so as to take variations in sea temperature and salinity into account in the calculation of hydrodynamic forces. With this in mind, a thorough critical analysis of the influence of sea temperature and salinity on hydrodynamic forces on piles like those used nowadays in offshore wind farms will be carried out. This influence on hydrodynamic forces occurs through a change in water density and viscosity due to temperature and salinity variation. Therefore, the aim here is to observe whether models currently used to estimate wave forces on piles are valid for different ranges of sea temperature and salinity apart from observing the limit when diffraction or nonlinear effects arise combining both effects with the magnitude of the pile diameter. Hence, specific software has been developed to simulate equations in fluid mechanics taking into account nonlinear and diffraction effects. This software enables wave produced forces on a cylinder supported on the sea bed to be calculated. The study includes observations on the calculation model's sensitivity as to a variation in the cylinder's diameter, on the one hand and, on the other, as to temperature and salinity variation. This software will enable an iterative calculation to be made for finding out the shape the pressure wave caused when a wave passes over will have for different pile diameters and water with different temperature and salinity.

A numerical scheme to calculate temperature and salinity dependent air-water transfer velocities for any gas

Directory of Open Access Journals (Sweden)

M. T. Johnson

2010-10-01

Full Text Available The ocean-atmosphere flux of a gas can be calculated from its measured or estimated concentration gradient across the air-sea interface and the transfer velocity (a term representing the conductivity of the layers either side of the interface with respect to the gas of interest. Traditionally the transfer velocity has been estimated from empirical relationships with wind speed, and then scaled by the Schmidt number of the gas being transferred. Complex, physically based models of transfer velocity (based on more physical forcings than wind speed alone, such as the NOAA COARE algorithm, have more recently been applied to well-studied gases such as carbon dioxide and DMS (although many studies still use the simpler approach for these gases, but there is a lack of validation of such schemes for other, more poorly studied gases. The aim of this paper is to provide a flexible numerical scheme which will allow the estimation of transfer velocity for any gas as a function of wind speed, temperature and salinity, given data on the solubility and liquid molar volume of the particular gas. New and existing parameterizations (including a novel empirical parameterization of the salinity-dependence of Henry's law solubility are brought together into a scheme implemented as a modular, extensible program in the R computing environment which is available in the supplementary online material accompanying this paper; along with input files containing solubility and structural data for ~90 gases of general interest, enabling the calculation of their total transfer velocities and component parameters. Comparison of the scheme presented here with alternative schemes and methods for calculating air-sea flux parameters shows good agreement in general. It is intended that the various components of this numerical scheme should be applied only in the absence of experimental data providing robust values for parameters for a particular gas of interest.

A numerical scheme to calculate temperature and salinity dependent air-water transfer velocities for any gas

Science.gov (United States)

Johnson, M. T.

2010-10-01

The ocean-atmosphere flux of a gas can be calculated from its measured or estimated concentration gradient across the air-sea interface and the transfer velocity (a term representing the conductivity of the layers either side of the interface with respect to the gas of interest). Traditionally the transfer velocity has been estimated from empirical relationships with wind speed, and then scaled by the Schmidt number of the gas being transferred. Complex, physically based models of transfer velocity (based on more physical forcings than wind speed alone), such as the NOAA COARE algorithm, have more recently been applied to well-studied gases such as carbon dioxide and DMS (although many studies still use the simpler approach for these gases), but there is a lack of validation of such schemes for other, more poorly studied gases. The aim of this paper is to provide a flexible numerical scheme which will allow the estimation of transfer velocity for any gas as a function of wind speed, temperature and salinity, given data on the solubility and liquid molar volume of the particular gas. New and existing parameterizations (including a novel empirical parameterization of the salinity-dependence of Henry's law solubility) are brought together into a scheme implemented as a modular, extensible program in the R computing environment which is available in the supplementary online material accompanying this paper; along with input files containing solubility and structural data for ~90 gases of general interest, enabling the calculation of their total transfer velocities and component parameters. Comparison of the scheme presented here with alternative schemes and methods for calculating air-sea flux parameters shows good agreement in general. It is intended that the various components of this numerical scheme should be applied only in the absence of experimental data providing robust values for parameters for a particular gas of interest.

Isotopic and chemical investigations of quaternary aquifer in sinai peninsula

International Nuclear Information System (INIS)

Sadek, M.A.; Ahmed, M.A.; Awad, M.A.

2001-01-01

The present study has been conducted to investigate the renewal activity and mineralization potential of the quaternary aquifer in Sinai peninsula using environmental isotopes and hydrochemistry. The quaternary aquifer is vital for development processes as it has a wide extension and shallow water table. The total dissolved salts vary greatly from one location to another and range widely between 510-7060 mg/1, reflecting all categories from fresh to saline water. The change in salinity all over Sinai can be attributed to variations in the rate of evaporation. Leaching and dissolution of terrestrial salts during floods as well as the effects of sea spray and saline water intrusion. The main sources of groundwater recharge are the infiltration of Local precipitation and surface runoff as well as lateral flow through hydraulic connection with fractured aquifers. Snow melt also contributes to aquifer recharge in some areas in the central part of southern Sinai. The environmental stable isotopic contents of the ground water in the quaternary aquifer in Sinai reflect the isotopic composition of rain water from continental and east Mediterranean precipitation and monsonal air mass which comes from Indian ocean as well as the seepage of partly evaporated floodwater. The southern samples are more suitable for drinking and irrigation purposes due to its lower salinity and sodium hazard

Seasonal plant water uptake patterns in the saline southeast Everglades ecotone.

Science.gov (United States)

Ewe, Sharon M L; Sternberg, Leonel da S L; Childers, Daniel L

2007-07-01

The purpose of this study was to determine the seasonal water use patterns of dominant macrophytes coexisting in the coastal Everglades ecotone. We measured the stable isotope signatures in plant xylem water of Rhizophora mangle, Cladium jamaicense, and Sesuvium portulacastrum during the dry (DS) and wet (WS) seasons in the estuarine ecotone along Taylor River in Everglades National Park, FL, USA. Shallow soilwater and deeper groundwater salinity was also measured to extrapolate the salinity encountered by plants at their rooting zone. Average soil water oxygen isotope ratios (delta(18)O) was enriched (4.8 +/- 0.2 per thousand) in the DS relative to the WS (0.0 +/- 0.1 per thousand), but groundwater delta(18)O remained constant between seasons (DS: 2.2 +/- 0.4 per thousand; WS: 2.1 +/- 0.1 per thousand). There was an inversion in interstitial salinity patterns across the soil profile between seasons. In the DS, shallow water was euhaline [i.e., 43 practical salinity units (PSU)] while groundwater was less saline (18 PSU). In the WS, however, shallow water was fresh (i.e., 0 PSU) but groundwater remained brackish (14 PSU). All plants utilized 100% (shallow) freshwater during the WS, but in the DS R. mangle switched to a soil-groundwater mix (delta 55% groundwater) while C. jamaicense and S. portulacastrum continued to use euhaline shallow water. In the DS, based on delta(18)O data, the roots of R. mangle roots were exposed to salinities of 25.4 +/- 1.4 PSU, less saline than either C. jamaicense (39.1 +/- 2.2 PSU) or S. portulacastrum (38.6 +/- 2.5 PSU). Although the salinity tolerance of C. jamaicense is not known, it is unlikely that long-term exposure to high salinity is conducive to the persistence of this freshwater marsh sedge. This study increases our ecological understanding of how water uptake patterns of individual plants can contribute to ecosystem levels changes, not only in the southeast saline Everglades, but also in estuaries in general in response to

Age of ground water and the origin of its salinity in the Leba region

International Nuclear Information System (INIS)

Kwaterkiewicz, A.; Sadurski, A.; Zuber, A.

1999-01-01

Intensive exploitation of ground waters in the Leba region caused a strong increase of salinity, which on the basis of hydrochemistry, was supposed to result from the intrusion of the Baltic Sea water. Environmental isotope data revealed that water in the tertiary sediments is of glacial origin and its salinity is related to the admixture of ascending older waters. (author)

Density functional theory calculations of H/D isotope effects on polymer electrolyte membrane fuel cell operations

Energy Technology Data Exchange (ETDEWEB)

Yanase, Satoshi; Oi, Takao [Sophia Univ., Tokyo (Japan). Faculty of Science and Technology

2015-10-01

To elucidate hydrogen isotope effects observed between fuel and exhaust hydrogen gases during polymer electrolyte membrane fuel cell operations, H-to-D reduced partition function ratios (RPFRs) for the hydrogen species in the Pt catalyst phase of the anode and the electrolyte membrane phase of the fuel cell were evaluated by density functional theory calculations on model species of the two phases. The evaluation yielded 3.2365 as the value of the equilibrium constant of the hydrogen isotope exchange reaction between the two phases at 39 C, which was close to the experimentally estimated value of 3.46-3.99 at the same temperature. It was indicated that H{sup +} ions on the Pt catalyst surface of the anode and H species in the electrolyte membrane phase were isotopically in equilibrium with one another during fuel cell operations.

Calculations of energy levels and electromagnetic properties for tellurium pair isotopes, by unified method

International Nuclear Information System (INIS)

Teixeira, R.R.P.

1988-01-01

Calculations with the Unified Model (vibrator coupled to two particles), of the energy levels and the eletromagnetic properties have been performed and compared with the twelve pair isotopes from tellurium with A between 112 and 134. The results were analysed using as particles interaction: pairing and SDI (Surface Delta Interaction). The SDI and 3 fonons collective states were used in the fittings, and a syntematic comparison between the theoretical and experimental results was made. The dependence of the results with the model parameters was determined, through large variation sof them. Calculations using 4 fonons have been made, and the importance of the introduced variations in the results was discussed. Calculations have been made in the VAX Computer of the Pelletron at IFUSP. (author) [pt

Application of isotope techniques to investigate groundwater pollution in India

International Nuclear Information System (INIS)

Shivanna, K.; Navada, S.V.; Kulkarni, K.M.; Sinha, U.K.; Sharma, S.

1998-01-01

Environmental isotopes ( 2 H, 18 O, 34 S, 3 H, and 14 C) techniques have been used along with hydrogeology and hydrochemistry to investigate: (a). the source of salinity and origin of sulphate in groundwaters of coastal Orissa, Orissa State, India and (b) to study the source of salinity in deep saline groundwaters of charnockite terrain at Kokkilimedu, South of Chennai, India. In the first case, as a part of large drinking water supply project, thousands of hand pumps were installed from 1985. Many of them became quickly unacceptable for potable supply due to salinity, increased iron and sulphate contents of the groundwater. In this alluvial, multiaquifer system, fresh, brackish and saline groundwaters occur in a rather complicated fashion. The conditions change from phreatic to confined flowing type with increasing depth. The results of the isotope geochemical investigation indicate that the shallow groundwater (depth/<50m) is fresh and modern. Groundwater salinity in intermediate aquifer (50 - 100m) is due to the Flandrian transgression during Holocene period. Fresh and modern deep groundwater forms a well developed aquifer which receives recharge through weathered basement rock. The saline groundwater found below the fresh deep aquifer have marine water entrapped during late Pleistocene. The source of high sulphate in the groundwater is of marine origin. In the second case, under the host rock characterization programme, the charnockite rock formation at Kokkilimedu, Kalpakkam was evaluated to assess its suitability as host medium for location of a geological repository for high level radioactive waste. Four deep boreholes were drilled in this area, the depth varying from 200 to 618 m. In these boreholes, large variations in groundwater salinity were observed over a distance of only a few hundred meters and no regional pattern could be identified. The results of the isotope investigation show that there are two different sources of salinity in this area. Among

Measurement of N{sub 2} fixation in Sesbania aculeata pers. and Sorghum bicolor L. grown in intercropping system, under saline conditions, using {sup 15}N isotopic dilution technique

Energy Technology Data Exchange (ETDEWEB)

Kurdali, F; Khalifa, K; Janat, M [Atomic Energy Commission, Damascus (Syrian Arab Republic). Dept. of Agriculture

2001-09-01

A field experiment was conducted under saline conditions (soil EC{sub e} 15, water EC{sub w} 8 dS/m/m) to evaluate the performance of sole crops and inter crops of Sesbania aculeata and Sorghum bicolor (1:1 row ratio) in terms of dry matter production, total N yield, soil N uptake and N{sub 2}-fixation using {sup 15}N isotope dilution method. Dry matter yield in sole crop of sesbania was significantly higher that that of sole sorghum; whereas, that of the inter cropping was significantly lower than sole sesbania, but was similar to that produced by sole sorghum. Total nitrogen yield in sole sesbania was four-fold than that accumulated in sole sorghum, whereas, that of mixed cropping was 2.6 fold compared to that of sole sorghum. The LER of total N yield was higher than 1 reflecting a greater advantage of inter cropping system in terms of land use efficiency. The proportion of N derived from N{sub 2} fixation (%Ndfa) in the sesbania was increased from 63 to 79%, for sole and inter cropping system, respectively. There was no evidence of a significant transfer of N from the sesbania to the sorghum. Results on the relative growth of plants on saline soil compared with non-saline soil clearly demonstrated that sesbania was more salt tolerant than the sorghum. soil nitrogen uptake by plants, particularly in sorghum, was adversely affected by salinity. However, amounts of N{sub 2} fixed by sole sesbania grown is saline soil was close or even higher than on non-saline soil. The use of inter cropping systems of legumes and non-legumes could be a promising agricultural approach to reutilize wasted lands, after a careful selection of appropriate tolerant genotypes to prevailing saline conditions. (author)

Estimates of matter yield and N-uptake in sorghum grown on saline and non-saline soils manured with dhaincha (sesbania aculeata) plant residues utilizing 15N tracer techniques

International Nuclear Information System (INIS)

Kurdali, F.

2002-11-01

Pot experiments were conducted to study the effect of manuring with three types of plant residues (roots, shoots or roots plus shoots) of Dhaincha (Sesbania aculeata Pers.) on the yield and N-uptake of Sorghum bicolor grown in saline and non-saline soils. For measuring various sources of N-uptake, two isotopic dilution techniques were utilized by adding to these soils either 15 N-labelled inorganic N-fertilizer (indirect method) or 15 N-labelled sesbania leaves (direct method). For the indirect method, both soils manured with each type of sesbania residue, received four split applications of 15 N-labelled ammonium sulphate. Results indicated that each type of sesbania residue, applied as a green manure, resulted in significant increases in both dry matter yield and N-uptake of sorghum as compared with the un manured control. Moreover, sesbania residues decreased the harmful effect of salinity on plant growth. Percentages of N derived from residues (%Ndfr) in sorghum grown in non saline soil ranged between 3.9 and 33%; whereas, in saline soil, the observed values ranged between 4.9 and 19.8%. N recoveries in sorghum grown in non saline soil were 61, 45 and 37% of the total amount contained in the sesbania root, shoot and root plus shoot; whereas, values in sorghum grown in saline soils were 48, 14,8 and 15.7%, respectively. The beneficial effects of sesbania residues have been attributed not only to the additional N availability to the plants, but also to its effects on the enhancement of soil N uptake. Percentages and amounts of Ndfr calculated using the indirect method were not significantly different from those obtained by the direct method indicating that the indirect method used herein is feasible and simple for measuring N release from organic residues. It is suggested that the use of Sesbania aculeata residues, particularly the shoots, as a green manure, can provide a substantial portion of total N in sorghum. Moreover, the use of sesbania green manure in

Calculations of the energy spectra of Zn, Ga and Ge isotopes by the shell model

International Nuclear Information System (INIS)

Sakakura, M.; Shikata, Y.; Arima, A.; Sebe, T.

1979-01-01

The effective Hamiltonian which was determined empirically by Koops and Glaudemans is tested in shell model calculations for the 65-68 Zn, 67-69 Ga, and 68-70 Ge nuclei in the full (1p 3 / 2 , 0f 5 / 2 , 1p 1 / 2 )n space. The resulting energy spectra are compared with the experimental spectra and results of previous calculations. The overall agreement with experiment is as satisfactory for these nuclei as for the Ni and Cu isotopes, by which the Hamiltonian was determined. It is noticed that the spectra of 67 Zn and 67 , 69 Ga calculated in this work are similar to those provided by the Alaga model. (orig.) [de

Comparison of the Sr isotopic signatures in brines of the Canadian and Fennoscandian shields

International Nuclear Information System (INIS)

Negrel, Philippe; Casanova, Joel

2005-01-01

A synthesis of Sr isotope data from shallow and deep groundwaters, and brines from the Fennoscandian and Canadian Shields is presented. A salinity gradient is evident in the water with concentrations varying from approximately 1-75 g L -1 below 1500 m depth in the Fennoscandian Shield and from 10 up to 300 g L -1 below 650 m depth in the Canadian Shield. Strontium isotope ratios were measured to assess the origin of the salinity and evaluate the degree of water-rock interaction in the systems. In both shields, the Sr concentrations are enriched relative to Cl, defining a positive trend parallel to the seawater dilution line and indicative of Sr addition through weathering processes. The depth distribution for Sr concentration increases strongly with increasing depth in both shields although the variation in Sr-isotope composition does not mirror that of Sr concentrations. Strontium-isotope compositions are presented for surface waters, and groundwaters in several sites in the Fennoscandian and Canadian Shields. Numerous mixing lines can be drawn reflecting water-rock interaction. A series of calculated lines links the surface end-members (surface water and shallow groundwater) and the deep brines; these mixing lines define a range of 87 Sr/ 86 Sr ratios for the deep brines in different selected sites. All sites show a specific 87 Sr/ 86 Sr signature and the occurrence of large 87 Sr/ 86 Sr variations is site specific in both shields. In Canadian Shield brines, the Sr isotope ratios clearly highlight large water rock interaction that increases the 87 Sr/ 86 Sr ratio from water that could have been of marine origin. In contrast to the Canadian Shield, groundwater does not occur in closed pockets in the Fennoscandian, and the well-constrained 87 Sr/ 86 Sr signatures in deep brines should correspond to a large, well-mixed and homogeneous water reservoir, whose Sr isotope signature results from water-rock interaction

Precipitation, flood- and groundwaters of the Negev highlands. An isotopic study of desert hydrology

International Nuclear Information System (INIS)

Levin, M.; Issar, A.

1980-01-01

Precipitation in the Negev highlands was found to be surprisingly depleted of 18 O and deuterium and generally characterized by ''deuterium excess'' values of d>15per mille. Isotopic compositions are relatively uniform over a wide area on any particular day, but differ appreciably from storm to storm. Thus, they are valuable tools for hydrographic analysis of flood-flows. Flood-flow samples, collected in Nahal-Zin and Nahal-Besor, were often even more depleted in heavy isotopes than the total rainstorm, indicating that run-off is generated selectively by high-intensity rains. The initial rush of the flood flushed away the surface salinity and saline accumulations in surface pools, but apparently does not involve sub-surface salinity to any great extent. Recharge to groundwater appears to be accompanied by a slight evaporative enrichment of the isotopes, more so in the case of waters recharged from flood-flows. Environmental tritium can be used as an indicator of direct flood-water contributions to the aquifers. (author)

Isotopic clusters

International Nuclear Information System (INIS)

Geraedts, J.M.P.

1983-01-01

Spectra of isotopically mixed clusters (dimers of SF 6 ) are calculated as well as transition frequencies. The result leads to speculations about the suitability of the laser-cluster fragmentation process for isotope separation. (Auth.)

Fractionation of boron isotopes in Icelandic hydrothermal systems

International Nuclear Information System (INIS)

Aggarwal, J.K.

1995-01-01

Boron isotope ratios have been determined in a variety of different geothermal waters from hydrothermal systems across Iceland. Isotope ratios from the high temperature meteoric water recharged systems reflect the isotope ratio of the host rocks without any apparent fractionation. Seawater recharged geothermal systems exhibit more positive δ 1 1B values than the meteoric water recharged geothermal systems. Water/rock ratios can be assessed from boron isotope ratios in the saline hydrothermal systems. Low temperature hydrothermal systems also exhibit more positive δ 1 1B than the high temperature systems, indicating fractionation of boron due to absorption of the lighter isotope onto secondary minerals. Fractionation of boron in carbonate deposits may indicate the level of equilibrium attained within the systems. (author). 14 refs., 2 figs

Inventory of programs. Calculation of the isotope inventory after a hypothetical accident at the Cofrentes Nuclear power

International Nuclear Information System (INIS)

Albendea, M.

2014-01-01

Iberdrola is developing a new application to calculate the inventory of radiological material, then of a hypothetical accident, with the name of inventory. This application allows you to calculate the inventory isotopic, analysers and accurate thermal of all or part of the nucleus of the plant of Cofrentes, even of any single element, based on its history of irradiation and specific periods of decay, since the reactor at any time after the shutdown. (Author)

Isotopic analyses and calculation by use of JENDL-3.2 for high burn-up UO2 and MOX spent fuels

International Nuclear Information System (INIS)

Sasahara, Akihiro; Matsumura, Tetsuo; Nicolaou, G.; Betti, M.; Walker, C.T.

1997-01-01

The post irradiation examinations (PIE) were carried out for high burn-up UO 2 spent fuel (3.8%U235, average burn-up:60GWd/t) and mixed oxide (MOX) spent fuel (5.07%Pu, average burn-up:45GWd/t). The PIE includes, a) isotopic analysis, b) electron probe microanalysis (EPMA) in pellet cross section and so on. The results of isotopic analyses and EPMA were compared with ORIGEN2/82 and VIM-BURN calculation results. In VIM-BURN calculation, the nuclear data of actinides were proceeded from new data file, JENDL-3.2. The sensitivities of power history and moderator density to nuclides composition were investigated by VIM-BURN calculation and consequently power history mainly effected on Am241 and Am242m and moderator density effected on fissile nuclides. From EPMA results of U and Pu distribution in pellet, VIM-BURN calculation showed reasonable distribution in pellet cross section. (author)

Origin of Boron and Brine Evolution in Saline Springs in the Nangqen Basin, Southern Tibetan Plateau

Directory of Open Access Journals (Sweden)

Ji-long Han

2018-01-01

Full Text Available The Nangqen Basin is a typical shearing-extensional basin situated in the hinterland of the Tibetan Plateau. It contains abundant saline spring resources and abnormal trace element enrichments. The hydrochemical molar ratios (Na/Cl, B/Cl, and Br/Cl, H-O isotopes, and B isotopes of the saline spring were systematically measured to describe the evolution of brines and the origin of the boron. The sodium chloride coefficient of the water samples in this area is around 1.0 or slightly greater, which is characteristic of leached brines; the highest B/Cl value is 4.25 (greater than that of seawater. The Na/Cl, B/Cl, and Br/Cl values of the springs are clear indicators of a crustal origin. The δ18O values of the spring waters range from −12.88‰ to −16.05‰, and the δD values range from −100.91‰ to −132.98‰. Meanwhile the B content and B isotopes in the saline springs are in the ranges of 1.00 to 575.56 ppm and +3.55‰ to +29.59‰, respectively. It has been proven that the saline springs in the Nangqen Basin are a type of leached brine, suggesting that the saline springs have a terrestrial origin. The δ11B-B characteristics of the springs are similar to those observed in the Tibetan geothermal area, indicating that these two places have the same B source. Moreover, they have a crustal origin (marine carbonate rocks and volcanic rocks instead of a deep mantle source.

Rearing conditions and habitat use of white seabass (Atractoscion nobilis) in the northeastern Pacific based on otolith isotopic composition

Science.gov (United States)

Romo-Curiel, Alfonsina E.; Herzka, Sharon Z.; Sepulveda, Chugey A.; Pérez-Brunius, Paula; Aalbers, Scott A.

2016-03-01

White seabass, Atractoscion nobilis, is an important coastal resource throughout both California and Baja California, but whether this species comprises a single or multiple subpopulations in the northeastern Pacific is not known. The aim of this study was to infer larval rearing habitats and population structure of white seabass by sampling adults from three regions spanning a latitudinal temperature gradient and a distance of over 1000 km, and analyzing the isotopic composition (δ18O and δ13C) of otolith aragonite corresponding to the larval, juvenile and adult stages. Otolith cores revealed high isotopic variability and no significant differences among regions, suggesting overlapping rearing conditions during the larval stage, the potential for long distance dispersal or migration or selective mortality of larvae at higher temperatures. Back-calculated temperatures of aragonite precipitation derived using regional salinity-δw relationships and local salinity estimates also did not differ significantly. However, there were significant differences between the δ18O values of the first seasonal growth ring of age 0 fish as well as back-calculated aragonite precipitation temperatures, suggesting the presence of two potentially discrete subpopulations divided by Punta Eugenia (27°N) along the central Baja California peninsula. These findings are consistent with regional oceanographic patterns and are critical for understanding white seabass population structure, and provide information needed for the implementation of appropriate management strategies.

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

Science.gov (United States)

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

2015-12-01

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

Foraminifera isotopic records... with special attention to high northern latitudes and the impact of sea-ice distillation processes

Energy Technology Data Exchange (ETDEWEB)

Hillaire-Marcel, Claude, E-mail: hillaire-marcel.claude@uqam.ca [GEOTOP, Universite du Quebec a Montreal, PO Box 8888, succursale ' centre ville' Montreal, Qc, H3C 3P8 (Canada)

2011-05-15

Since the reassessment of oxygen isotope paleotemperatures by N. Shackleton in the late 60s, most papers using isotopic records from planktic or benthic foraminifers imply a direct relationship between oxygen isotopes in seawater and the ice/ocean volume, thus some linkage with salinity, sea level, etc. Such assumptions are also made when incorporating 'isotopic modules' in coupled models. Here, we will further examine the linkages between salinity and oxygen isotope ratios of sea-water recorded by foraminifers, and their potential temporal and spatial variability, especially in the northern North Atlantic and the Arctic oceans. If temporal and spatial changes in the isotopic composition of precipitations and ice meltwaters tune the isotopic properties of the fresh water end-member that dilutes the ocean, rates of sea-ice formation and evaporation at the ocean surface play a further role on the salt and oxygen isotope contents of water masses. Thus, the oxygen 18-salinity relationship carries a specific isotopic signature for any given water mass. At the ocean scale, residence time and mixing of these water masses, as well as the time dependent-achievement of proxy-tracer equilibrium, will also result in variable recordings of mass transfers into the hydrosphere, notable between ice-sheets and ocean. Since these records in water mass may vary in both amplitude and time, direct correlations of isotopic records will potentially be misleading. Implications of such issues on the interpretation of oxygen isotope records from the sub-arctic seas will be discussed, as well as the inherent flaws of such records due to sedimentological and or ecological parameters.

Origin of water salinity in the coastal Sarafand aquifer (South-Lebanon)

International Nuclear Information System (INIS)

Hashash, Adnan; Aranyossy, J.F.

1996-01-01

Author.The geochemical and isotopic study, based on the analysis of twenty water samples from well in the coastal plain of Sarafand (South-Lebanon), permit to eliminate the hypothesis of marine intrusion in this aquifer. The increase of salinity observed in certain wells is due to the contamination of cretaceous aquifer water by the quaternary formations. The two poles of mixing are respectively characterized: by weak tritium contents (between 2 and 3 UT) and a value of stable isotopes (-5,9<0,18<-5,5) corresponding to the appearance of cretaceous formation area; by the high tritium contents and enrichment relative to heavy isotope in the mineralized water of superficial formations. On the other hand, the isotope contents permit the set a rapid renewal of the cretaceous aquifer water due to quick circulation in the Karstic system

Expanded uncertainty associated with determination of isotope enrichment factors: Comparison of two point calculation and Rayleigh-plot.

Science.gov (United States)

Julien, Maxime; Gilbert, Alexis; Yamada, Keita; Robins, Richard J; Höhener, Patrick; Yoshida, Naohiro; Remaud, Gérald S

2018-01-01

The enrichment factor (ε) is a common way to express Isotope Effects (IEs) associated with a phenomenon. Many studies determine ε using a Rayleigh-plot, which needs multiple data points. More recent articles describe an alternative method using the Rayleigh equation that allows the determination of ε using only one experimental point, but this method is often subject to controversy. However, a calculation method using two points (one experimental point and one at t 0 ) should lead to the same results because the calculation is derived from the Rayleigh equation. But, it is frequently asked "what is the valid domain of use of this two point calculation?" The primary aim of the present work is a systematic comparison of results obtained with these two methodologies and the determination of the conditions required for the valid calculation of ε. In order to evaluate the efficiency of the two approaches, the expanded uncertainty (U) associated with determining ε has been calculated using experimental data from three published articles. The second objective of the present work is to describe how to determine the expanded uncertainty (U) associated with determining ε. Comparative methodologies using both Rayleigh-plot and two point calculation are detailed and it is clearly demonstrated that calculation of ε using a single data point can give the same result as a Rayleigh-plot provided one strict condition is respected: that the experimental value is measured at a small fraction of unreacted substrate (f < 30%). This study will help stable isotope users to present their results in a more rigorous expression: ε ± U and therefore to define better the significance of an experimental results prior interpretation. Capsule: Enrichment factor can be determined through two different methods and the calculation of associated expanded uncertainty allows checking its significance. Copyright © 2017 Elsevier B.V. All rights reserved.

Salinity of irrigation water in the Philippi farming area of the Cape ...

African Journals Online (AJOL)

Salinity of irrigation water in the Philippi farming area of the Cape Flats, Cape Town, ... Isotope analysis was done for the summer samples so as to assess effects of ... It is concluded that the accumulation of salts in groundwater and soil in the ...

Salinity controls on Na incorporation in Red Sea planktonic foraminifera

Science.gov (United States)

Mezger, E. M.; de Nooijer, L. J.; Boer, W.; Brummer, G. J. A.; Reichart, G. J.

2016-12-01

Whereas several well-established proxies are available for reconstructing past temperatures, salinity remains challenging to assess. Reconstructions based on the combination of (in)organic temperature proxies and foraminiferal stable oxygen isotopes result in relatively large uncertainties, which may be reduced by application of a direct salinity proxy. Cultured benthic and planktonic foraminifera showed that Na incorporation in foraminiferal shell calcite provides a potential independent proxy for salinity. Here we present the first field calibration of such a potential proxy. Living planktonic foraminiferal specimens from the Red Sea surface waters were collected and analyzed for their Na/Ca content using laser ablation quadrupole inductively coupled plasma mass spectrometry. Using the Red Sea as a natural laboratory, the calibration covers a broad range of salinities over a steep gradient within the same water mass. For both Globigerinoides ruber and Globigerinoides sacculifer calcite Na/Ca increases with salinity, albeit with a relatively large intraspecimen and interspecimen variability. The field-based calibration is similar for both species from a salinity of 36.8 up to 39.6, while values for G. sacculifer deviate from this trend in the northernmost transect. It is hypothesized that the foraminifera in the northernmost part of the Red Sea are (partly) expatriated and hence should be excluded from the Na/Ca-salinity calibration. Incorporation of Na in foraminiferal calcite therefore provides a potential proxy for salinity, although species-specific calibrations are still required and more research on the effect of temperature is needed.

Isotopic analyses and calculation by use of JENDL-3.2 for high burn-up UO{sub 2} and MOX spent fuels

Energy Technology Data Exchange (ETDEWEB)

Sasahara, Akihiro; Matsumura, Tetsuo [Central Research Inst. of Electric Power Industry, Komae, Tokyo (Japan). Komae Research Lab.; Nicolaou, G.; Betti, M.; Walker, C.T.

1997-03-01

The post irradiation examinations (PIE) were carried out for high burn-up UO{sub 2} spent fuel (3.8%U235, average burn-up:60GWd/t) and mixed oxide (MOX) spent fuel (5.07%Pu, average burn-up:45GWd/t). The PIE includes, (a) isotopic analysis, (b) electron probe microanalysis (EPMA) in pellet cross section and so on. The results of isotopic analyses and EPMA were compared with ORIGEN2/82 and VIM-BURN calculation results. In VIM-BURN calculation, the nuclear data of actinides were proceeded from new data file, JENDL-3.2. The sensitivities of power history and moderator density to nuclides composition were investigated by VIM-BURN calculation and consequently power history mainly effected on Am241 and Am242m and moderator density effected on fissile nuclides. From EPMA results of U and Pu distribution in pellet, VIM-BURN calculation showed reasonable distribution in pellet cross section. (author)

A box model of the Late Miocene Mediterranean Sea: implications from combined 87Sr/86Sr and salinity data

NARCIS (Netherlands)

Topper, R.P.M.; Flecker, R.; Meijer, P.Th.; Wortel, M.J.R.

2011-01-01

Under certain conditions the strontium isotope ratio in the water of a semi‐enclosed basin is known to be sensitive to the relative size of ocean water inflow and river input. Combining Sr‐isotope ratios measured in Mediterranean Late Miocene successions with data on past salinity, one can derive

Tomographic, hydrochemical and isotopic investigations of the ...

Indian Academy of Sciences (India)

An electrical imaging tomography survey was carried out to identify the lateral and vertical salinity distribution in the oasis shallow aquifers of the Nefzaoua region located in southwestern Tunisia. In addition, hydrochemical and isotopic data were examined to determine the main factors and mechanisms controlling the ...

Seeking excellence: An evaluation of 235 international laboratories conducting water isotope analyses by isotope-ratio and laser-absorption spectrometry.

Science.gov (United States)

Wassenaar, L I; Terzer-Wassmuth, S; Douence, C; Araguas-Araguas, L; Aggarwal, P K; Coplen, T B

2018-03-15

Water stable isotope ratios (δ 2 H and δ 18 O values) are widely used tracers in environmental studies; hence, accurate and precise assays are required for providing sound scientific information. We tested the analytical performance of 235 international laboratories conducting water isotope analyses using dual-inlet and continuous-flow isotope ratio mass spectrometers and laser spectrometers through a water isotope inter-comparison test. Eight test water samples were distributed by the IAEA to international stable isotope laboratories. These consisted of a core set of five samples spanning the common δ-range of natural waters, and three optional samples (highly depleted, enriched, and saline). The fifth core sample contained unrevealed trace methanol to assess analyst vigilance to the impact of organic contamination on water isotopic measurements made by all instrument technologies. For the core and optional samples ~73 % of laboratories gave acceptable results within 0.2 ‰ and 1.5 ‰ of the reference values for δ 18 O and δ 2 H, respectively; ~27 % produced unacceptable results. Top performance for δ 18 O values was dominated by dual-inlet IRMS laboratories; top performance for δ 2 H values was led by laser spectrometer laboratories. Continuous-flow instruments yielded comparatively intermediate results. Trace methanol contamination of water resulted in extreme outlier δ-values for laser instruments, but also affected reactor-based continuous-flow IRMS systems; however, dual-inlet IRMS δ-values were unaffected. Analysis of the laboratory results and their metadata suggested inaccurate or imprecise performance stemmed mainly from skill- and knowledge-based errors including: calculation mistakes, inappropriate or compromised laboratory calibration standards, poorly performing instrumentation, lack of vigilance to contamination, or inattention to unreasonable isotopic outcomes. To counteract common errors, we recommend that laboratories include 1-2 'known

Seeking excellence: An evaluation of 235 international laboratories conducting water isotope analyses by isotope-ratio and laser-absorption spectrometry

Science.gov (United States)

Wassenaar, L. I.; Terzer-Wassmuth, S.; Douence, C.; Araguas-Araguas, L.; Aggarwal, P. K.; Coplen, Tyler B.

2018-01-01

RationaleWater stable isotope ratios (δ2H and δ18O values) are widely used tracers in environmental studies; hence, accurate and precise assays are required for providing sound scientific information. We tested the analytical performance of 235 international laboratories conducting water isotope analyses using dual-inlet and continuous-flow isotope ratio mass spectrometers and laser spectrometers through a water isotope inter-comparison test.MethodsEight test water samples were distributed by the IAEA to international stable isotope laboratories. These consisted of a core set of five samples spanning the common δ-range of natural waters, and three optional samples (highly depleted, enriched, and saline). The fifth core sample contained unrevealed trace methanol to assess analyst vigilance to the impact of organic contamination on water isotopic measurements made by all instrument technologies.ResultsFor the core and optional samples ~73 % of laboratories gave acceptable results within 0.2 ‰ and 1.5 ‰ of the reference values for δ18O and δ2H, respectively; ~27 % produced unacceptable results. Top performance for δ18O values was dominated by dual-inlet IRMS laboratories; top performance for δ2H values was led by laser spectrometer laboratories. Continuous-flow instruments yielded comparatively intermediate results. Trace methanol contamination of water resulted in extreme outlier δ-values for laser instruments, but also affected reactor-based continuous-flow IRMS systems; however, dual-inlet IRMS δ-values were unaffected.ConclusionsAnalysis of the laboratory results and their metadata suggested inaccurate or imprecise performance stemmed mainly from skill- and knowledge-based errors including: calculation mistakes, inappropriate or compromised laboratory calibration standards, poorly performing instrumentation, lack of vigilance to contamination, or inattention to unreasonable isotopic outcomes. To counteract common errors, we recommend that

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

Digital Repository Service at National Institute of Oceanography (India)

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

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

Use of microwave remote sensing in salinity estimation

International Nuclear Information System (INIS)

Singh, R.P.; Kumar, V.; Srivastav, S.K.

1990-01-01

Soil-moisture interaction and the consequent liberation of ions causes the salinity of waters. The salinity of river, lake, ocean and ground water changes due to seepage and surface runoff. We have studied the feasibility of using microwave remote sensing for the estimation of salinity by carrying out numerical calculations to study the microwave remote sensing responses of various models representative of river, lake and ocean water. The results show the dependence of microwave remote sensing responses on the salinity and surface temperature of water. The results presented in this paper will be useful in the selection of microwave sensor parameters and in the accurate estimation of salinity from microwave remote sensing data

Strontium isotopic signatures of oil-field waters: Applications for reservoir characterization

Science.gov (United States)

Barnaby, R.J.; Oetting, G.C.; Gao, G.

2004-01-01

The 87Sr/86Sr compositions of formation waters that were collected from 71 wells producing from a Pennsylvanian carbonate reservoir in New Mexico display a well-defined distribution, with radiogenic waters (up to 0.710129) at the updip western part of the reservoir, grading downdip to less radiogenic waters (as low as 0.708903 to the east. Salinity (2800-50,000 mg/L) displays a parallel trend; saline waters to the west pass downdip to brackish waters. Elemental and isotopic data indicate that the waters originated as meteoric precipitation and acquired their salinity and radiogenic 87Sr through dissolution of Upper Permian evaporites. These meteoric-derived waters descended, perhaps along deeply penetrating faults, driven by gravity and density, to depths of more than 7000 ft (2100 m). The 87 Sr/86Sr and salinity trends record influx of these waters along the western field margin and downdip flow across the field, consistent with the strong water drive, potentiometric gradient, and tilted gas-oil-water contacts. The formation water 87Sr/86Sr composition can be useful to evaluate subsurface flow and reservoir behavior, especially in immature fields with scarce pressure and production data. In mature reservoirs, Sr Sr isotopes can be used to differentiate original formation water from injected water for waterflood surveillance. Strontium isotopes thus provide a valuable tool for both static and dynamic reservoir characterization in conjunction with conventional studies using seismic, log, core, engineering, and production data. Copyright ??2004. The American Association of Petroleum Geologist. All rights reserved.

Ab Initio Nuclear Structure and Reaction Calculations for Rare Isotopes

Energy Technology Data Exchange (ETDEWEB)

Draayer, Jerry P. [Louisiana State Univ., Baton Rouge, LA (United States)

2014-09-28

We have developed a novel ab initio symmetry-adapted no-core shell model (SA-NCSM), which has opened the intermediate-mass region for ab initio investigations, thereby providing an opportunity for first-principle symmetry-guided applications to nuclear structure and reactions for nuclear isotopes from the lightest p-shell systems to intermediate-mass nuclei. This includes short-lived proton-rich nuclei on the path of X-ray burst nucleosynthesis and rare neutron-rich isotopes to be produced by the Facility for Rare Isotope Beams (FRIB). We have provided ab initio descriptions of high accuracy for low-lying (including collectivity-driven) states of isotopes of Li, He, Be, C, O, Ne, Mg, Al, and Si, and studied related strong- and weak-interaction driven reactions that are important, in astrophysics, for further understanding stellar evolution, X-ray bursts and triggering of s, p, and rp processes, and in applied physics, for electron and neutrino-nucleus scattering experiments as well as for fusion ignition at the National Ignition Facility (NIF).

Ab Initio Nuclear Structure and Reaction Calculations for Rare Isotopes

International Nuclear Information System (INIS)

Draayer, Jerry P.

2014-01-01

We have developed a novel ab initio symmetry-adapted no-core shell model (SA-NCSM), which has opened the intermediate-mass region for ab initio investigations, thereby providing an opportunity for first-principle symmetry-guided applications to nuclear structure and reactions for nuclear isotopes from the lightest p-shell systems to intermediate-mass nuclei. This includes short-lived proton-rich nuclei on the path of X-ray burst nucleosynthesis and rare neutron-rich isotopes to be produced by the Facility for Rare Isotope Beams (FRIB). We have provided ab initio descriptions of high accuracy for low-lying (including collectivity-driven) states of isotopes of Li, He, Be, C, O, Ne, Mg, Al, and Si, and studied related strong- and weak-interaction driven reactions that are important, in astrophysics, for further understanding stellar evolution, X-ray bursts and triggering of s, p, and rp processes, and in applied physics, for electron and neutrino-nucleus scattering experiments as well as for fusion ignition at the National Ignition Facility (NIF).

Crop improvement for salinity and drought tolerance using nuclear and related techniques (abstract)

International Nuclear Information System (INIS)

Serraj, R.; Lagoda, P.J.

2005-01-01

complex interactions among the traits involved in tolerance to both drought and salinity, pyramiding using marker-assisted breeding, induced mutation and other biotechnologies, combined with a multidisciplinary approach and the participation of farmers, is likely to provide the best strategy to accelerate the progress towards the development of adapted tolerant crop germplasm. The joint FAO/IAEA division is investing considerable effort in evaluating opportunities for using nuclear and related technologies to improve tolerance to abiotic stresses such as drought and salinity. The division has a long-standing experience in developing and coordinating collaborative research programs (CRP) on abiotic stresses, involving NARs in developing countries, international IARCs and expert scientists. Similarly, several technical cooperation projects (TCP) were carried out on crop improvement for tolerance to drought and salinity, at national, regional and interregional levels. The Soil and Biotechnology laboratories at Seibersdorf also have the experience and facilities for developing, testing and applying new isotope and nuclear-related techniques for the improvement of crop productivity and stress tolerance. An important project is currently being implemented by the joint FAO/IAEA division for the identification and development of crop germplasm with superior resource use efficiency and nutritional value and adapted to harsh environments. Two CRPs have been recently launched under this project dealing respectively with (i) the identification and pyramiding of mutated genes, and novel approaches for improving crop tolerance to salinity and drought, and (II) the selection for greater agronomic water-use efficiency in wheat and rice using carbon isotope discrimination under drought and saline environments. This paper will review the recent progress made at the joint FAO/IAEA division in deciphering the complexity of drought and salinity problems and developing drought and salt

A global algorithm for estimating Absolute Salinity

Science.gov (United States)

McDougall, T. J.; Jackett, D. R.; Millero, F. J.; Pawlowicz, R.; Barker, P. M.

2012-12-01

The International Thermodynamic Equation of Seawater - 2010 has defined the thermodynamic properties of seawater in terms of a new salinity variable, Absolute Salinity, which takes into account the spatial variation of the composition of seawater. Absolute Salinity more accurately reflects the effects of the dissolved material in seawater on the thermodynamic properties (particularly density) than does Practical Salinity. When a seawater sample has standard composition (i.e. the ratios of the constituents of sea salt are the same as those of surface water of the North Atlantic), Practical Salinity can be used to accurately evaluate the thermodynamic properties of seawater. When seawater is not of standard composition, Practical Salinity alone is not sufficient and the Absolute Salinity Anomaly needs to be estimated; this anomaly is as large as 0.025 g kg-1 in the northernmost North Pacific. Here we provide an algorithm for estimating Absolute Salinity Anomaly for any location (x, y, p) in the world ocean. To develop this algorithm, we used the Absolute Salinity Anomaly that is found by comparing the density calculated from Practical Salinity to the density measured in the laboratory. These estimates of Absolute Salinity Anomaly however are limited to the number of available observations (namely 811). In order to provide a practical method that can be used at any location in the world ocean, we take advantage of approximate relationships between Absolute Salinity Anomaly and silicate concentrations (which are available globally).

Calculation and analysis of neutron and radiation characteristics of lead coolants with isotopic tailoring for future nuclear power facilities

Energy Technology Data Exchange (ETDEWEB)

Blokhin, A.I.; Ivanov, A.P.; Korobeinikov, V.V.; Lunev, V.P.; Manokhin, V.N.; Khorasanov, G.L. [SSC RF A. I. Leypunsky Institute for Physics and Power Engineering, Obninsk, Kaluga Region (Russian Federation)

2000-03-01

A new type of safe fast reactor with lead coolant was proposed in Russia. The use of coolants with low moderating properties is one of the ways to get a hard neutron spectrum and an increase in the burning of Np-237, Am-243 and other miner actinides(MA) fissionable preferentially in the fast reactor. The stable lead isotope, Pb-208, is proposed as the one of such coolants. The neutron inelastic scattering cross-section of Pb-208 is 3.0-3.5 times less than the one of other lead isotopes. Calculation of the MA transmutation rates in the standard BN-type fast reactor with different coolants is performed by Monte-Carlo method using Code MMKFK. Six various models are simulated for the fast reactor blanket with different kinds of fuel and coolant. The fast reactor with natural-lead coolant practically does not differ from the reactor with sodium coolant relative to MA incineration. The use of Pb-208 as a coolant in the fast reactor results in increasing incineration of MA from 18 to 26% in comparison with a usual fast reactor. Calculation of induced radioactivity was performed using the FISPACT-3 inventory code, also. The results include total induced radioactivity and dose rate for initial material composition and selected long-lived radionuclides. The calculations show that the coolant consisting of lead isotope, Pb-206, or Pb-207, can be considered as the low-activation one because it does not practically contain long-lived toxic radionuclides. (M. Suetake)

Hydrochemical and physical processes influencing salinization and freshening in Mediterranean low-lying coastal environments

NARCIS (Netherlands)

Mollema, P.N.; Antonelli, M.; Dinelli, E.; Gabbianelli, G.; Greggio, N.; Stuijfzand, P.J.

2013-01-01

Ground- and surface water chemistry and stable isotope data from the coastal zone near Ravenna (Italy) have been examined to determine the geochemical conditions and processes that occur and their implications for fresh water availability in the various brackish/saline coastal environments. Fresh

Using environmental isotopes along with major hydro-geochemical compositions to assess deep groundwater formation and evolution in eastern coastal China

Science.gov (United States)

Xu, Naizheng; Gong, Jianshi; Yang, Guoqiang

2018-01-01

Hydrochemical analysis and environmental isotopic tracing are successfully applied to study groundwater evolution processes. Located in eastern China, the Jiangsu Coastal Plain is characterized by an extensively exploited deep groundwater system, and groundwater salinization has become the primary water environmental problem. This paper provides a case study on the use of a hydrochemical and environmental isotopic approach to assess possible mixing and evolution processes at Yoco Port, Jiangsu Province, China. Hydrochemical and isotopic patterns of deep groundwater allow one to distinguish different origins in deep water systems. HCO3- is the dominant anion in the freshwater samples, whereas Na+ and Cl- are the dominant major ions in the saline samples. According to δ18O, δ2H and 14C dating, the fresh water is derived from precipitation under a colder climate during the Glacial Maximum (Dali Glacial), while the saline groundwater is influenced by glacial-interglacial cycles during the Holocene Hypsithermal. The δ18O, δ2H and 3H data confirm that deep groundwater in some boreholes is mixed with overlying saline water. The deep groundwater reservoir can be divided into a saline water sector and a fresh water sector, and each show distinct hydrochemical and isotopic compositions. The saline groundwater found in the deep aquifer cannot be associated with present seawater intrusion. Since the Last Glacial Maximum in the Late Pleistocene, the deep groundwater flow system has evolved to its current status with the decrease in ice cover and the rising of sea level. However, the hydraulic connection is strengthened by continuous overexploitation, and deep groundwater is mixed with shallow groundwater at some points.

Rate-controlling two-proton transfer coupled with heavy-atom motion in the 2-pyridinone-catalyzed mutarotation of tetramethylglucose. Experimental and calculated deuterium isotope effects

International Nuclear Information System (INIS)

Engdahl, K.A.; Bivehed, H.; Ahlberg, P.; Saunders, W.H. Jr.

1983-01-01

Primary and secondary deuterium isotope effects have been measured by polarimetry, and primary isotope effects have been calculated for the classical bifunctional catalysis: 2-pyridinone-catalyzed mutarotation of 2,3,4,6-tetra-O-methyl-α-D-glucopyranose (α-TMG) in benzene. From the positively curved plot of the specific rate of epimerization vs. the mole fraction of 2 H in the ''pool'' of OH and NH hydrogens, the isotope effects k/sub HH//k/sub DD/ = 3.66 +/- 0.09, k/sub HH//k/sub DH/ = 1.5, and k/sub HH//k/sub HD/ = 2.4 have been calculated. A secondary isotope effect of 1.14 +/- 0.02 has been measured by using α-TMG and (1- 2 H)-2,3,4,6-tetra-O-methyl-α-D-glucopyranose [(l- 2 H)-α-TMG], the synthesis of which is described in detail, together with those for (N- 2 H)-2-pyridinone and (1-O- 2 H)-2,3,4,6-tetra-O-methyl-α-D-glucopyranose [(1-O- 2 H)-α-TMG]. The rate data obtained have also been analyzed by fractionation theory, yielding approximately equal fractionation factors (0.5). The interpretation of the results has been assisted by calculations of the primary deuterium isotope effects using the BEBOVIB IV program. Two models involving small and considerable coupling, respectively, of the transferring protons to heavy-atom motion have been considered. In the favored structure for the transition state of the rate-limiting step, two protons are in transit, and their motion is governed either by a potential with a barrier or by one without. Their motion is considerably coupled to the heavy-atom motion (i.e., the breakage of the ring C-O bond), and tunnel corrections to the isotope effects are found to be negligible

Ground-water pollution determined by boron isotope systematics

International Nuclear Information System (INIS)

Vengosh, A.; Kolodny, Y.; Spivack, A.J.

1998-01-01

Boron isotopic systematics as related to ground-water pollution is reviewed. We report isotopic results of contaminated ground water from the coastal aquifers of the Mediterranean in Israel, Cornia River in north-western Italy, and Salinas Valley, California. In addition, the B isotopic composition of synthetic B compounds used for detergents and fertilizers was investigated. Isotopic analyses were carried out by negative thermal ionization mass spectrometry. The investigated ground water revealed different contamination sources; underlying saline water of a marine origin in saline plumes in the Mediterranean coastal aquifer of Israel (δ 11 B=31.7 per mille to 49.9 per mille, B/Cl ratio ∼1.5x10 -3 ), mixing of fresh and sea water (25 per mille to 38 per mille, B/Cl∼7x10 -3 ) in saline water associated with salt-water intrusion to Salinas Valley, California, and a hydrothermal contribution (high B/Cl of ∼0.03, δ 11 B=2.4 per mille to 9.3 per mille) in ground water from Cornia River, Italy. The δ 11 B values of synthetic Na-borate products (-0.4 per mille to 7.5 per mille) overlap with those of natural Na-borate minerals (-0.9 per mille to 10.2 per mille). In contrast, the δ 11 B values of synthetic Ca-borate and Na/Ca borate products are significantly lower (-15 per mille to -12.1 per mille) and overlap with those of the natural Ca-borate minerals. We suggest that the original isotopic signature of the natural borate minerals is not modified during the manufacturing process of the synthetic products, and it is controlled by the crystal chemistry of borate minerals. The B concentrations in pristine ground-waters are generally low ( 11 B=39 per mille), salt-water intrusion and marine-derived brines (40 per mille to 60 per mille) are sharply different from hydrothermal fluids (δ 11 B=10 per mille to 10 per mille) and anthropogenic sources (sewage effluent: δ 11 B=0 per mille to 10 per mille; boron-fertilizer: δ 11 B=-15 per mille to 7 per mille). some

Shape coexistence in selenium isotopes

International Nuclear Information System (INIS)

Liu Ying; Cao Zhongbin; Xu Furong

2010-01-01

Nuclear shape change and shape coexistence in the Selenium isotopes have been investigated by Total-Routhian-Surface (TRS) calculations. It is found that nuclear shapes vary significantly with increasing neutron number. The TRS calculations for the ground states of 66,72,92,94 Se isotopes show that both neutron-deficient and neutron-dripline Selenium isotopes have oblate and prolate shape coexistence. The cranking shell-model calculations for 72,94 Se give that prolate and oblate shape coexistence in low rotational frequency. However, oblate rotational bands disappear and prolate rotational bands become yrast bands with increasing rotational frequency, which is due to the intrusion of the g 9/2 orbitals. (authors)

A global algorithm for estimating Absolute Salinity

Directory of Open Access Journals (Sweden)

T. J. McDougall

2012-12-01

Full Text Available The International Thermodynamic Equation of Seawater – 2010 has defined the thermodynamic properties of seawater in terms of a new salinity variable, Absolute Salinity, which takes into account the spatial variation of the composition of seawater. Absolute Salinity more accurately reflects the effects of the dissolved material in seawater on the thermodynamic properties (particularly density than does Practical Salinity.

When a seawater sample has standard composition (i.e. the ratios of the constituents of sea salt are the same as those of surface water of the North Atlantic, Practical Salinity can be used to accurately evaluate the thermodynamic properties of seawater. When seawater is not of standard composition, Practical Salinity alone is not sufficient and the Absolute Salinity Anomaly needs to be estimated; this anomaly is as large as 0.025 g kg⁻¹ in the northernmost North Pacific. Here we provide an algorithm for estimating Absolute Salinity Anomaly for any location (x, y, p in the world ocean.

To develop this algorithm, we used the Absolute Salinity Anomaly that is found by comparing the density calculated from Practical Salinity to the density measured in the laboratory. These estimates of Absolute Salinity Anomaly however are limited to the number of available observations (namely 811. In order to provide a practical method that can be used at any location in the world ocean, we take advantage of approximate relationships between Absolute Salinity Anomaly and silicate concentrations (which are available globally.

Parameter Identification for Salinity in a Quasilinear Thermodynamic System of Sea Ice

OpenAIRE

Wei Lv; Xiaojiao Li; Enmin Feng

2014-01-01

This study is intended to provide a parameter identification method to determine salinity of sea ice by temperature and salinity observations. A quasilinear thermodynamic system of sea ice with unknown salinity is described and its property is proved. Then, a parameter identification model is established and the existence of its optimal solution is discussed. The salinity profile is calculated by the temperature and salinity data, which were measured at Nella Fjord around Zhongshan Station, A...

AUTOSECOL: an automatic calculation of the self-shielding of heavy isotope resonances

International Nuclear Information System (INIS)

Grandotto-Biettoli, Marc.

The formalism is based on separating both types of resonance effects: local energy effects creating a fine structure in the flux, and bulk effects resulting in a slow variation in the flux. Effective reaction rates are defined that, used as tables in a multigroup calculation of cells with a large pitch in regard to resonance widths, allow an exact account of the dependence of the effective integral upon fast variations in the flux. These tables are used to introduce this phenomenon of resonance self-shielding in the multigroup Apollo program for solving the neutron transport equation, they are derived from nuclear data with using some parameters relating to the physical state of the resonant isotope inside the fuel medium. The AUTOSECOL system provides a library of effective reaction rates for taking account of the resonance self-shielding effect on the neutron flux in nuclear reactor cells. Its versatility in regard to the methods previously used for solving the same problem allows a rapid testing of the consequences of considering the self-shielding effect of new isotope resonances, a following up of the evolution in nuclear data evaluation, and rapidly studying the interest lying in new data. Results obtained with AUTOSECOL are compared with those obtained when using the SECOL code for computing the effective reaction rates of 235 U, 239 Pu, 107 Ag, 109 Ag, and 241 Pu [fr

Study, using stable isotopes, of flow distribution, surface-groundwater relations and evapotranspiration in the Okavango Swamp, Botswana

International Nuclear Information System (INIS)

Dincer, T.; Hutton, L.G.; Kupee, B.B.J.

1979-01-01

Stable isotope data collected in the Okavango Delta have confirmed that the central distributary system is more active at present than the peripheral systems. The data also show that there is no groundwater outflow at the western and southern margins of the delta. A salinity-isotope model of the deltaic swamp has been developed to study the relation between the salinity and isotopic composition of the swamp waters. An attempt has been made to separate the atmospheric losses from the swamp into its evapotranspiration components. The results indicate that in winter, when high water levels prevail, these losses are almost entirely due to evaporation whilst in summer, when the water levels are low, evaporation and transpiration contribute almost equally to the total atmospheric losses. (author)

Calculations of kinetic isotope effects in the syn-eliminations of (2-phenylethyl)dimethylamine oxides

International Nuclear Information System (INIS)

Shafiei-Kermani, H.R.

1987-01-01

Transition state theory (TST) calculations of kinetic isotope effects (KIE) for the syn-elimination of (2-phenylethyl)dimethylamine oxides have been carried out for a series of transition state (TS) models encompassing both E1-like and E1cB-like regions of the E2 mechanistic spectrum. A large number of different reaction coordinates were explored for both unsolvated and for coordination of solvent dimethylsulfoxide in the cyclic transition state models. The models of reaction for both solvated and unsolvated models of proton transfer are presented. A simplified method for easier initial screening of reaction coordinate contributions is developed, discussed, and found to produce accurate approximations to the full model KIE values. Both unsolvated and solvated models show E1-like E2 mechanism and the calculated values from both models are in extremely good agreement with experimentally measured KIE. Both models were used to investigate para-substituted derivatives (Z = CL, OCH 3 ) of the parent compound (Z = H). The transition states are related by a shift in structure parallel to the central E2 diagonal of an O'Ferrall-Jencks-Fry reaction diagram, as predicted by Thornton, indicating that in the absence of other factors, the extent to which negative charge is accumulated at C/sub β/ in the transition state is a function primarily of the leaving group. All of the structural parameters such as bond distances and bond angles were related to independent bond orders. Beta-deuterium isotope effects produced by both solvated and nonsolvated models are temperature dependent

Ab initio calculation of the transition-state properties and addition rate constants for H + C2H2 and selected isotopic analogues

International Nuclear Information System (INIS)

Harding, L.B.; Wagner, A.F.; Bowman, J.M.; Schatz, G.C.; Christoffel, K.

1982-01-01

GVB-POL-CI ab initio calculations of the geometries, energetics, and normal mode frequencies of C 2 H 2 , C 2 H 3 , and the transition state for the addition reaction of H + C 2 H 2 are presented. In addition, normal mode frequencies for the isotopic variants D + C 2 D 2 , D + C 2 H 2 , and H + C 2 D 2 are preented. These results are compared to experimental values for C 2 H 2 and to ab initio values of Hagase and Kern, and semiempirical values of Keil, Lynch, Cowfer, and Michael. The results are also used to calculate the apparent bimolecular addition rate constant using conventional RRKM theory for chemical activation. The calculated rate constants and their isotopic variants are compared as a function of temperature and pressure to available experimental information. The agreement is little different from that obtained by Keil et al. with a similar calculation using semiempirical values for acetylene, transition-state, and vinyl radical properties. In particular, the calculated high-pressure limit of the rate constant appears to be at least 1 order of magnitude higher than the experimental limit. Several possible reasons for this discrepancy are discussed

Multi-proxy paleoenvironmental reconstruction of saline lake carbonates: Paleoclimatic and paleogeographic implications (Priabonian-Rupelian, Issirac Basin, SE France)

Science.gov (United States)

Lettéron, Alexandre; Fournier, François; Hamon, Youri; Villier, Loïc; Margerel, Jean-Pierre; Bouche, Alexandre; Feist, Monique; Joseph, Philippe

2017-08-01

A 200-m thick carbonate succession has been deposited in shallow-water, saline lake environments during the Priabonian-Rupelian in the Issirac Basin (South-East France). The palaeoenvironmental and palaeogeographic significance of such saline lake carbonates has been characterized on the basis of a multi-proxy analysis including 1) depositional and diagenetic features, 2) biological components (molluscs, ostracods, benthic foraminifers, characean) and 3) carbon, oxygen and strontium stable isotopes. Biological associations are indicative of dominantly shallow (climate (dry versus humid) are the three key factors controlling the water composition, carbonate production and depositional environments in the Issirac lake. Although the ASCI (Alès-Issirac-Saint-Chaptes) lacustrine system likely represents an athalassic (inland) lake system evolving through times, the stable isotope composition (C, O and Sr) of carbonates strongly suggests the occurrence of transient connections of the ASCI lake water with water bodies influenced by seawater and/or fed with sulfates deriving from Triassic evaporites. The Issirac Basin may be therefore interpreted as a sill area connecting the ASCI lacustrine system with the Rhône valley (Mormoiron and Valence) saline lake systems during maximum flooding periods. Finally, changes in depositional features, biota and stable isotope composition of carbonates in unit U3 suggest a transition from relatively dry to more humid climate during the uppermost Priabonian or earliest Rupelian.

Response of lupine plants irrigated with saline water to rhizobium inoculation using 15N-isotope dilution

International Nuclear Information System (INIS)

Gadalla, A.M.; El-Ghandour, I.A.; Abdel Aziz, H.A.; Hamdy, A.; Aly, M.M.

2002-01-01

The lupine Rhizobium symbiosis and contribution of N 2 fixation under different levels of irrigation water salinity were examined. Lysimeter experiment was established under greenhouse conditions during the year 2002-2003. In this experiment, inoculated plants were imposed to different salinity levels of irrigation water and N-fertilizer treatment. Plant height was decreased under different salinity levels, nitrogen treatments and bacterial inoculation. Similar trend was noticed with leaf area. The highest leaf area was recorded with salt tolerant bacterial inoculation (SBI) and splitting N-treatment. Highest values of N-uptake occurred after 100 day intervals under the tested factors. Relative decrease in N-uptake did not exceed 40% of those recorded with the fresh water treatment as affected by experimental factors. Nitrogen uptake by the whole plant reflected an increase at 3 dS/m salinity level of irrigation water. Relative increases were 5% and 15% for normal bacteria inoculation under single dose (NI) and splitting

Organic matter dynamics along a salinity gradient in Siberian steppe soils

Science.gov (United States)

Bischoff, Norbert; Mikutta, Robert; Shibistova, Olga; Dohrmann, Reiner; Herdtle, Daniel; Gerhard, Lukas; Fritzsche, Franziska; Puzanov, Alexander; Silanteva, Marina; Grebennikova, Anna; Guggenberger, Georg

2018-01-01

Salt-affected soils will become more frequent in the next decades as arid and semiarid ecosystems are predicted to expand as a result of climate change. Nevertheless, little is known about organic matter (OM) dynamics in these soils, though OM is crucial for soil fertility and represents an important carbon sink. We aimed at investigating OM dynamics along a salinity and sodicity gradient in the soils of the southwestern Siberian Kulunda steppe (Kastanozem, non-sodic Solonchak, Sodic Solonchak) by assessing the organic carbon (OC) stocks, the quantity and quality of particulate and mineral-associated OM in terms of non-cellulosic neutral sugar contents and carbon isotopes (δ13C, 14C activity), and the microbial community composition based on phospholipid fatty acid (PLFA) patterns. Aboveground biomass was measured as a proxy for plant growth and soil OC inputs. Our hypotheses were that (i) soil OC stocks decrease along the salinity gradient, (ii) the proportion and stability of particulate OM is larger in salt-affected Solonchaks compared to non-salt-affected Kastanozems, (iii) sodicity reduces the proportion and stability of mineral-associated OM, and (iv) the fungi : bacteria ratio is negatively correlated with salinity. Against our first hypothesis, OC stocks increased along the salinity gradient with the most pronounced differences between topsoils. In contrast to our second hypothesis, the proportion of particulate OM was unaffected by salinity, thereby accounting for only soil types, while mineral-associated OM contributed > 90 %. Isotopic data (δ13C, 14C activity) and neutral sugars in the OM fractions indicated a comparable degree of OM transformation along the salinity gradient and that particulate OM was not more persistent under saline conditions. Our third hypothesis was also rejected, as Sodic Solonchaks contained more than twice as much mineral-bound OC than the Kastanozems, which we ascribe to the flocculation of OM and mineral components under

Salinization and dilution history of ground water discharging into the Sea of Galilee, the Dead Sea Transform, Israel

International Nuclear Information System (INIS)

Bergelson, G.; Nativ, R.; Bein, A.

1999-01-01

The mechanism governing salinization of ground water discharging into the Sea of Galilee in Israel has been the subject of debate for several decades. Because the lake provides 25% of the water consumed annually in Israel, correct identification of the salt sources is essential for the establishment of suitable water-management strategies for the lake and the ground water in the surrounding aquifers. Existing salinization models were evaluated in light of available and newly acquired data including general chemistry, and O, H, C and Cl isotopes. Based on the chemical and isotopic observations, the proposed salt source is an ancient, intensively evaporated brine (21- to 33-fold seawater) which percolated through the valley formations from a lake which had formed in the Rift Valley following seawater intrusion during the late Miocene. Low Na:Cl and high Br:Cl values support the extensive evaporation, whereas high Ca:Cl and low Mg:Cl values indicate the impact of dolomitization of the carbonate host rock on the residual solution. Based on radiocarbon and other isotope data, the dilution of the original brine occurred in two stages: the first took place similar30andpuncsp; omitted000 a ago by slightly evaporated fresh-to-brackish lake water to form the Sea of Galilee Brine. The second dilution phase is associated with the current hydrological regime as the Sea of Galilee Brine migrates upward along the Rift faults and mixes with the actively circulating fresh ground water to form the saline springs. The spatially variable chemical and isotopic features of the saline springs suggest not only differential dilution by fresh meteoric water, but also differential percolation timing of the original brine into the tectonically disconnected blocks, registering different evaporation stages in the original brine. Consequently, various operations to reduce the brine contribution to the lake may be differentially effective in the various areas. (Copyright (c) 1999 Elsevier Science

Hydraulic lift and tolerance to salinity of semiarid species: consequences for species interactions.

Science.gov (United States)

Armas, Cristina; Padilla, Francisco M; Pugnaire, Francisco I; Jackson, Robert B

2010-01-01

The different abilities of plant species to use ephemeral or permanent water sources strongly affect physiological performance and species coexistence in water-limited ecosystems. In addition to withstanding drought, plants in coastal habitats often have to withstand highly saline soils, an additional ecological stress. Here we tested whether observed competitive abilities and C-water relations of two interacting shrub species from an arid coastal system were more related to differences in root architecture or salinity tolerance. We explored water sources of interacting Juniperus phoenicea Guss. and Pistacia lentiscus L. plants by conducting physiology measurements, including water relations, CO2 exchange, photochemical efficiency, sap osmolality, and water and C isotopes. We also conducted parallel soil analyses that included electrical conductivity, humidity, and water isotopes. During drought, Pistacia shrubs relied primarily on permanent salty groundwater, while isolated Juniperus plants took up the scarce and relatively fresh water stored in upper soil layers. As drought progressed further, the physiological activity of Juniperus plants nearly stopped while Pistacia plants were only slightly affected. Juniperus plants growing with Pistacia had stem-water isotopes that matched Pistacia, unlike values for isolated Juniperus plants. This result suggests that Pistacia shrubs supplied water to nearby Juniperus plants through hydraulic lift. This lifted water, however, did not appear to benefit Juniperus plants, as their physiological performance with co-occurring Pistacia plants was poor, including lower water potentials and rates of photosynthesis than isolated plants. Juniperus was more salt sensitive than Pistacia, which withstood salinity levels similar to that of groundwater. Overall, the different abilities of the two species to use salty water appear to drive the outcome of their interaction, resulting in asymmetric competition where Juniperus is negatively

Identification of the mechanisms and origin of salinization of groundwaters in coastal aquifers by means of isotopic techniques; Identificacion de los mecanismos y del orgien de la salinizacion del agua subterranea en acuiferos costeros mdiante tecnicas isotopicas

Energy Technology Data Exchange (ETDEWEB)

Araguas, L. J.; Quejido, A. J.

2007-07-01

To study the origin of salinity and the mechanisms operating in coastal aquifers, a set of tools is available to determine the essential aspects of the hydrogeological behaviour of the system. these tools are based on the integrated use of hydrochemical parameters (major constituents and trace elements) and isotopic parameters (oxygen, hydrogen, sulfur, carbon, strontium and boron). In addition to the active intrusion of seawater, salinization in coastal areas may be influenced by various human activities that accelerate the degradation of water quality, such as concentrated pumping, intensive farming techniques with return of irrigation water, or reuse of urban and industrial waste water. Characterization of the dominant processes and mechanisms is required for suitable management of the resource and implementation of corrective measures. (Author)

Isotopic evaluation of ocean circulation in the Late Cretaceous North American seaway

Science.gov (United States)

Coulson, Alan B.; Kohn, Matthew J.; Barrick, Reese E.

2011-12-01

During the mid- and Late Cretaceous period, North America was split by the north-south oriented Western Interior Seaway. Its role in creating and maintaining Late Cretaceous global greenhouse conditions remains unclear. Different palaeoceanographic reconstructions portray diverse circulation patterns. The southward extent of relatively cool, low-salinity, low-δ18O surface waters critically distinguishes among these models, but past studies of invertebrates could not independently assess water temperature and isotopic compositions. Here we present oxygen isotopes in biophosphate from coeval marine turtle and fish fossils from western Kansas, representing the east central seaway, and from the Mississippi embayment, representing the marginal Tethys Ocean. Our analyses yield precise seawater isotopic values and geographic temperature differences during the main transition from the Coniacian to the early Campanian age (87-82 Myr), and indicate that the seaway oxygen isotope value and salinity were 2‰ and 3‰ lower, respectively, than in the marginal Tethys Ocean. We infer that the influence of northern freshwater probably reached as far south as Kansas. Our revised values imply relatively large temperature differences between the Mississippi embayment and central seaway, explain the documented regional latitudinal palaeobiogeographic zonation and support models with relatively little inflow of surface waters from the Tethys Ocean to the Western Interior Seaway.

Investigation of Lake Water Salinity by Using Four-Band Salinity Algorithm on WorldView-2 Satellite Image for a Saline Industrial Lake

Science.gov (United States)

Budakoǧlu, Murat; Karaman, Muhittin; Damla Uça Avcı, Z.; Kumral, Mustafa; Geredeli (Yılmaz), Serpil

2014-05-01

Salinity of a lake is an important characteristic since, these are potentially industrial lakes and the degree of salinity can significantly be used for determination of mineral resources and for the production management. In the literature, there are many studies of using satellite data for salinity related lake studies such as determination of salinity distribution and detection of potential freshwater sources in less salt concentrated regions. As the study area Lake Acigol, located in Denizli (Turkey) was selected. With it's saline environment, it's the major sodium sulphate production resource of Turkey. In this study, remote sensing data and data from a field study was used and correlated. Remote sensing is an efficient tool to monitor and analyze lake properties by using it complementary to field data. Worldview-2 satellite data was used in this study which consists of 8 bands. At the same time with the satellite data acquisition, a field study was conducted to collect the salinity values in 17 points of the laker with using YSI 556 Multiparametre for measurements. The values were measured as salinity amount in grams per kilogram solution and obtained as ppt unit. It was observed that the values vary from 34 ppt - 40.1 ppt and the average is 38.056 ppt. In Thalassic serie, the lake was in mixoeuhaline state in the time of issue. As a first step, ATCOR correction was performed on satellite image for atmospheric correction. There were some clouds on the lake field, hence it was decided to continue the study by using the 12 sampling points which were clear on the image. Then, for each sampling point, a spectral value was obtained by calculating the average at a 11*11 neighborhood. The relation between the spectral reflectance values and the salinity was investigated. The 4-band algorithm, which was used for determination of chlorophyll-a distribution in highly turbid coastal environment by Wei (2012) was applied. Salinity α (Λi-1 / Λj-1) * (Λk-1 / Λm-1) (i

Effect of salinity on 2H/1H fractionation in lipids from continuous cultures of the coccolithophorid Emiliania huxleyi

Science.gov (United States)

Sachs, Julian P.; Maloney, Ashley E.; Gregersen, Josh; Paschall, Christopher

2016-09-01

Salinity and temperature dictate the buoyancy of seawater, and by extension, ocean circulation and heat transport. Yet there remain few widely applicable proxies for salinity with the precision necessary to infer all but the largest hydrographic variations in the past. In the last decade the hydrogen isotope composition (2H/1H or δ2H) of microalgal lipids has been shown to increase systematically with salinity, providing a foundation for its use as a paleosalinity proxy. Culture and field studies have indicated a wide range of sensitivities for this response, ranging from about 0.6-3.3‰ ppt-1 depending on the lipid, location and/or culturing conditions. Lacking in these studies has been the controlled conditions necessary to isolate the response to salinity while keeping all other growth parameters constant. Here we show that the hydrogen isotope composition of lipids in the marine coccolithophorid Emiliania huxleyi grown in chemostats increased by 1.6 ± 0.3‰ ppt-1 (p huxleyi, which can be attributed to the fact that previous experiments were performed with batch cultures in which growth rates and other parameters differed between salinity treatments. The underlying cause of this response to salinity remains unknown, but may result from changes in (1) the proportion of lipid hydrogen derived from NADPH versus water, (2) the proportion of lipid hydrogen derived from NADPH from Photosystem I versus the oxidative pentose phosphate pathway (and other metabolic sources), or (3) the δ2H value of intracellular water.

Improved adiabatic calculation of muonic-hydrogen-atom cross sections. I. Isotopic exchange and elastic scattering in asymmetric collisions

International Nuclear Information System (INIS)

Cohen, J.S.; Struensee, M.C.

1991-01-01

The improved adiabatic representation is used in calculations of elastic and isotopic-exchange cross sections for asymmetric collisions of pμ, dμ, and tμ with bare p, d, and t nuclei and with H, D, and T atoms. This formulation dissociates properly, correcting a well-known deficiency of the standard adiabatic method for muonic-atom collisions, and includes some effects at zeroth order that are normally considered nonadiabatic. The electronic screening is calculated directly and precisely within the improved adiabatic description; it is found to be about 30% smaller in magnitude than the previously used value at large internuclear distances and to deviate considerably from the asymptotic form at small distances. The reactance matrices, needed for calculations of molecular-target effects, are given in tables

Determination of fission gas yields from isotope ratios

DEFF Research Database (Denmark)

Mogensen, Mogens Bjerg

1983-01-01

This paper describes a method of calculating the actual fission yield of Kr and Xe in nuclear fuel including the effect of neutron capture reactions and decay. The bases for this calculation are the cumulative yields (ref. 1) of Kr and Xe isotopes (or pairs of isotopes) which are unaffected...... by neutron capture reactions, and measured Kr and Xe isotope ratios. Also the burnup contribution from the different fissile heavy isotopes must be known in order to get accurate fission gas yields....

Thermodynamics of calcium-isotope-exchange reactions. 1. Exchange between isotopic calcium carbonates and aqueous calcium ions

International Nuclear Information System (INIS)

Zhang, R.S.; Nash, C.P.; Rock, P.A.

1988-01-01

This paper reports the authors results for the direct experimental determination of the equilibrium constant for the calcium-isotope-exchange reaction 40 CaCO 3 (s) + 44 CaCl 2 (aq) reversible 44 CaCO 2 (s) + 40 CaCl 2 (aq). The reaction was studied in electrochemical double cells without liquid junction of the type shown in eq 2. The experimental value of the equilibrium constant at 295 +/- 2 K is K = 1.08 +/- 0.02. The experimental value for K is compared with the values of K calculated for various model reactions according to the statistical thermodynamic theory of isotope effects. The isotopic solid carbonates were modeled according to both the Debye and Kieffer theories. No structured models of solvated isotopic aqueous calcium ions yield calculated equilibrium constants in agreement with their experimental results. This conclusion is in agreement with published molecular dynamics calculations which show that the aqueous solvation of Ca 2 =(aq) is essentially unstructured

Comparison of calculated and experimental isotope edited FTIR difference spectra for purple bacterial photosynthetic reaction centers with different quinones incorporated into the QA binding site.

Directory of Open Access Journals (Sweden)

Nan eZhao

2013-08-01

Full Text Available Previously we have shown that ONIOM type (QM/MM calculations can be used to simulate isotope edited FTIR difference spectra for neutral ubiquinone in the QA binding site in Rhodobacter sphaeroides photosynthetic reaction centers. Here we considerably extend upon this previous work by calculating isotope edited FTIR difference spectra for reaction centers with a variety of unlabeled and 18O labeled foreign quinones incorporated into the QA binding site. Isotope edited spectra were calculated for reaction centers with 2,3-dimethoxy-5,6-dimethyl-1,4-benzoquinone (MQ0, 2,3,5,6-tetramethyl-1,4-benzoquinone (duroquinone, DQ, and 2,3-dimethyl-l,4-naphthoquinone (DMNQ incorporated, and compared to corresponding experimental spectra. The calculated and experimental spectra agree well, further demonstrating the utility and applicability of our ONIOM approach for calculating the vibrational properties of pigments in protein binding sites.The normal modes that contribute to the bands in the calculated spectra, their composition, frequency and intensity, and how these quantities are modified upon 18O labeling, are presented. This computed information leads to a new and more detailed understanding/interpretation of the experimental FTIR difference spectra. Hydrogen bonding to the carbonyl groups of the incorporated quinones is shown to be relatively weak. It is also shown that there is some asymmetry in hydrogen bonding, accounting for 10-13 cm-1 separation in the frequencies of the carbonyl vibrational modes of the incorporated quinones. The extent of asymmetry H-bonding could only be established by considering the spectra for various types of quinones incorporated into the QA binding site. The quinones listed above are tail-less. Spectra were also calculated for reaction centers with corresponding tail containing quinones incorporated, and it is found that replacement of the quinone methyl group by a phytyl or prenyl chain does not alter ONIOM calculated s

Paleoclimatic and paleoceanographic studies of estuarine and marine sediments using strontium isotopes

International Nuclear Information System (INIS)

Ingram, B.L.

1992-01-01

Strontium isotopic ratio ( 87 Sr/ 86 Sr) measurements in fossil carbonates and phosphates are used to evaluate paleoceanographic and paleoclimatic environments in Quaternary, Pliocene-Pleistocene, and mid-Cretaceous estuarine and marine sediments. The use of 87 Sr/ 86 Sr measurements as an estuarine paleosalinity and paleoclimatic indicator is developed and applied to San Francisco Bay. 87 Sr/ 86 Sr measurements of foraminifer and molluscan fossils contained in estuarine sediments of late Pleistocene (ca 115 to 125 ka) and late Holocene (4.5 ka) age show cyclic variations indicating that salinity fluctuated with periods of several hundred years, probably reflecting wet-dry cycles associated with fluctuations in solar irradiance caused by sunspot cycles. The average salinity in San Pablo and Richardson bays was significantly lower (by 6 to 8%) over much of the past 4.5 ka than at present, reflecting a combination of decreased freshwater inflow at present associated with water diversion and wetter climatic conditions prior to 2000 years ago. Salinity data are converted to river discharge using salinity-delta flow relations derived from historical records for San Francisco Bay. The data indicate that annual freshwater inflow was at least twice the modern pre-diversion average between 2.5 and 3.0 Ka; this time period is also identified as one of wetter climatic conditions by lake level and treeline records from the Sierra Nevada. Strontium isotopic measurements of marine carbonate and fish teeth to middle Cretaceous age are used to increase the resolution of the existing seawater Sr isotope versus time curve and to assess models for global oceanic anoxic events. The new data using fish teeth show less scatter and variability than previous data. Negative excursions in the 87 Sr/ 86 Sr ratio of 7-14 parts in 10 -5 during Aptian anoxic events suggest a link between increased submarine volcanism and oceanic anoxia

Sources of Holocene variability of oxygen isotopes in paleoclimate archives

Directory of Open Access Journals (Sweden)

A. N. LeGrande

2009-08-01

Full Text Available Variability in water isotopes has been captured in numerous archives and used to infer past climate changes. Here we examine water isotope variability over the course of the Holocene using the water-isotope enabled, coupled atmosphere-ocean general circulation model, GISS ModelE-R. Eight Holocene time slices, ~1000 years apart are simulated and driven by estimated changes in orbital configuration, greenhouse gases, and ice sheet extent. We find that simulated water isotope archives match well with those seen in ice cores, ocean sediment cores, and speleothems. The climate changes associated with the water isotope changes, however, are more complex than simple modern spatial slope interpretations might suggest. In particular, water isotope variability in Asian speleothems is linked to alterations in landward water vapor transport, not local precipitation, and ice sheet changes over North America lead to the masking of temperature signals in Summit, Greenland. Salinity-seawater isotope variability is complicated by inter-ocean basin exchanges of water vapor. Water isotopes do reflect variability in the hydrology, but are better interpreted in terms of regional hydrological cycle changes rather than as indicators of local climate.

The integrated impacts of natural processes and human activities on groundwater salinization in the coastal aquifers of Beihai, southern China

Science.gov (United States)

Li, Qinghua; Zhang, Yanpeng; Chen, Wen; Yu, Shaowen

2018-03-01

Salinization in coastal aquifers is usually related to both seawater intrusion and water-rock interaction. The results of chemical and isotopic methods were combined to identify the origin and processes of groundwater salinization in Daguansha area of Beihai, southern China. The concentrations of the major ions that dominate in seawater (Cl-, Na+, Ca2+, Mg2+ and SO4 2- ), as well as the isotopic content and ratios (2H, 18O, 87Sr/86Sr and 13C), suggest that the salinization occurring in the aquifer of the coastal plain is related to seawater and that the prevailing hydrochemical processes are evaporation, mixing, dissolution and ion exchange. For the unconfined aquifer, groundwater salinization has occurred in an area that is significantly influenced by land-based sea farming. The integrated impacts of seawater intrusion from the Beibuwan Gulf and infiltration of seawater from the culture ponds are identified in the shallowest confined aquifer (I) in the middle of the area (site BBW2). Leakage from this polluted confined aquifer causes the salinization of groundwater in the underlying confined aquifer (II). At the coastal monitoring site (BBW3), confined aquifer I and lower confined aquifer II are heavily contaminated by seawater intrusion. The weak connectivity between the upper aquifers, and the seaward movement of freshwater, prevents saltwater from encroaching the deepest confined aquifer (III). A conceptual model is presented. Above all, understanding of the origin and processes of groundwater salinization will provide essential information for the planning and sustainable management of groundwater resources in this region.

Organic matter dynamics along a salinity gradient in Siberian steppe soils

Directory of Open Access Journals (Sweden)

N. Bischoff

2018-01-01

Full Text Available Salt-affected soils will become more frequent in the next decades as arid and semiarid ecosystems are predicted to expand as a result of climate change. Nevertheless, little is known about organic matter (OM dynamics in these soils, though OM is crucial for soil fertility and represents an important carbon sink. We aimed at investigating OM dynamics along a salinity and sodicity gradient in the soils of the southwestern Siberian Kulunda steppe (Kastanozem, non-sodic Solonchak, Sodic Solonchak by assessing the organic carbon (OC stocks, the quantity and quality of particulate and mineral-associated OM in terms of non-cellulosic neutral sugar contents and carbon isotopes (δ13C, 14C activity, and the microbial community composition based on phospholipid fatty acid (PLFA patterns. Aboveground biomass was measured as a proxy for plant growth and soil OC inputs. Our hypotheses were that (i soil OC stocks decrease along the salinity gradient, (ii the proportion and stability of particulate OM is larger in salt-affected Solonchaks compared to non-salt-affected Kastanozems, (iii sodicity reduces the proportion and stability of mineral-associated OM, and (iv the fungi : bacteria ratio is negatively correlated with salinity. Against our first hypothesis, OC stocks increased along the salinity gradient with the most pronounced differences between topsoils. In contrast to our second hypothesis, the proportion of particulate OM was unaffected by salinity, thereby accounting for only  <  10 % in all three soil types, while mineral-associated OM contributed  >  90 %. Isotopic data (δ13C, 14C activity and neutral sugars in the OM fractions indicated a comparable degree of OM transformation along the salinity gradient and that particulate OM was not more persistent under saline conditions. Our third hypothesis was also rejected, as Sodic Solonchaks contained more than twice as much mineral-bound OC than the Kastanozems, which we ascribe

Geochemical and isotopic characterization of the ground water of Oued Laya

International Nuclear Information System (INIS)

Hkiri, Sabrine

2010-01-01

In the Sahel region of Sousse (Tunisia Center East), almost all of the deep groundwater has undergone over the last decade, a general decline of groundwater level. This decrease is caused by two factors, the intensive farming and drought. These aquifers, despite their often poor quality (high salinity), are increasingly used, so they are now home to intense exploitation, whose consequences have emerged as significant declines of groundwater level and degradation of the chemical quality of their water. This study concerns a groundwater aquifer that is under stress and anthropogenic climate severe enough: the coastal aquifer of Wad Laya present quality of groundwater qualified low salinity point of view compared to other neighboring aquifers. The salinity is apparently not related to over exploitation as the majority of coastal aquifers but seems it is due to the geological nature which forms the water table. The region's climate is semiarid with an average annual rainfall of 320 mm by 100 years; the FTE is 1750 mm / year resulting in a water deficit of more than 1.4 m / year. Renewable resources are estimated at 3.3 million m3, while for the levy is estimated to be 2.7 million m3 which the dry residue is currently spent 5g / l (CRDA Sousse, 2009). The objective of this study included hydrogeological characterization of the aquifer using geophysical tools and identification of mechanisms of salination using geochemical and isotopic tools to determine the possible origins of mineralization. For this campaign sampling and measurement was made in the region over a thirty water points in order to measure the electrical conductivity, groundwater level and analyze the chemical composition (major and trace elements). Initial findings from this study are summarized in: Completion of piezometric maps and potentiometric study of the evolution in some wells show a decline of water table caused by the increased exploitation and lower rainfall, which resulted in an increase in

Detecting isotopic ratio outliers

Science.gov (United States)

Bayne, C. K.; Smith, D. H.

An alternative method is proposed for improving isotopic ratio estimates. This method mathematically models pulse-count data and uses iterative reweighted Poisson regression to estimate model parameters to calculate the isotopic ratios. This computer-oriented approach provides theoretically better methods than conventional techniques to establish error limits and to identify outliers.

Detecting isotopic ratio outliers

International Nuclear Information System (INIS)

Bayne, C.K.; Smith, D.H.

1986-01-01

An alternative method is proposed for improving isotopic ratio estimates. This method mathematically models pulse-count data and uses iterative reweighted Poisson regression to estimate model parameters to calculate the isotopic ratios. This computer-oriented approach provides theoretically better methods than conventional techniques to establish error limits and to identify outliers

Salinity effects on radiation utilization characteristics of Kochia (Kochia Scoparia L. Schrad.)

International Nuclear Information System (INIS)

Jami Al-Ahmadi, M.; Kafi, M.; Nassiri Mahalati, M.

2008-01-01

In order to evaluate light extinction coefficient and radiation use efficiency of Kochia scoparia in response to saline stress, a study was performed at Birjand, South Khorasan, using three levels of salinity in irrigation water (1.5, 8.6 and 28.2 dSm-1) with three replications. Several measurements were conducted during growth season to calculate radiation fraction passed through plant canopy, and also leaf area index (LAI) and total dry matter (TDM). Light extinction coefficient calculated with correcting fraction of plant light absorption for whole day, and using dry matter accumulation, radiation use efficiency obtained in each different salinity level. The results showed that light extinction coefficient of Kochia was equal to 0.59 for solar noon and 0.75 for whole day. The radiation absorption of kochia rose as LAI increased, and 95% of radiation was absorbed at LAI equal to 4 to 5. LAI and total dry matter accumulation were highest in moderate salinity level. In general, increase in salinity caused a delay in early season development, and accelerated plant maturity at late season. This caused plant canopies at the highest salinity reached to maximum light absorption later in growth season. Increase of salinity from 1.5 to 8.6 dSm-1 was responsible for little increase in RUE from 2.4 to 2.5 g per MJ absorbed PAR; however, it reduced with further increase in salinity. Thus, it seems that moderate salinity levels stimulate growth and dry matter accumulation of kochia and cause kochia canopy convert the absorbed radiation to dry matter more effectively. Key words: Kochia scoparia, Salinity, Light extension coefficient, Radiation use efficiency, Leaf Area Index

BSATOM - package of programs for calculating the energy levels and wave functions of helium-like systems taking into account isotope effects

International Nuclear Information System (INIS)

Abrashkevich, A.G.; Abrashkevich, D.G.; Vinitskij, S.I.; Puzynin, I.V.

1989-01-01

Description of package BCATOM for calculating the energy levels and wave functions of helium-like systems in the hyperspherical adiabatic approach taking into account the isotopic effects is given. The corresponding Sturm-Liouville problems are approximated by the difference method and the high order accuracy finite element method. The obtained generalized algebraic eigenvalue problems are solved by subspace iteration method. Possibilities of the package are demonstrated by calculating the ground state characteristics of a negative hydrogen ion. 33 refs.; 1 fig

Deformation properties of osmium, platinum, mercury isotopes from self-consistent calculations: influence of the pairing treatment

International Nuclear Information System (INIS)

Sauvage-Letessier, J.; Quentin, P.; Flocard, H.

1981-01-01

The deformation properties of several isotopes of the elements Os, Pt and Hg have been computed by means of Hartree-Fock plus BCS calculations. The Hartree-Fock potential has been derived from the Skyrme interaction S III. Two approximations have been used for the treatment of pairing correlations: the constant (versus deformation) gap method and the constant (versus deformation) pairing matrix element method. A good agreement with experimental data is obtained for ground state deformation properties except for the exact location of the prolate-oblate transition as a function of the neutron number. For one nucleus 184 Hg, the pairing matrix elements have been calculated from the Gogny interaction D1, in order to study their single particle state- and deformation-dependence. From these results, the validity of the two approximations used for pairing correlations, is discussed

A geochemical approach to determine sources and movement of saline groundwater in a coastal aquifer.

Science.gov (United States)

Anders, Robert; Mendez, Gregory O; Futa, Kiyoto; Danskin, Wesley R

2014-01-01

Geochemical evaluation of the sources and movement of saline groundwater in coastal aquifers can aid in the initial mapping of the subsurface when geological information is unavailable. Chloride concentrations of groundwater in a coastal aquifer near San Diego, California, range from about 57 to 39,400 mg/L. On the basis of relative proportions of major-ions, the chemical composition is classified as Na-Ca-Cl-SO4, Na-Cl, or Na-Ca-Cl type water. δ(2)H and δ(18)O values range from -47.7‰ to -12.8‰ and from -7.0‰ to -1.2‰, respectively. The isotopically depleted groundwater occurs in the deeper part of the coastal aquifer, and the isotopically enriched groundwater occurs in zones of sea water intrusion. (87)Sr/(86)Sr ratios range from about 0.7050 to 0.7090, and differ between shallower and deeper flow paths in the coastal aquifer. (3)H and (14)C analyses indicate that most of the groundwater was recharged many thousands of years ago. The analysis of multiple chemical and isotopic tracers indicates that the sources and movement of saline groundwater in the San Diego coastal aquifer are dominated by: (1) recharge of local precipitation in relatively shallow parts of the flow system; (2) regional flow of recharge of higher-elevation precipitation along deep flow paths that freshen a previously saline aquifer; and (3) intrusion of sea water that entered the aquifer primarily during premodern times. Two northwest-to-southeast trending sections show the spatial distribution of the different geochemical groups and suggest the subsurface in the coastal aquifer can be separated into two predominant hydrostratigraphic layers. © 2013, National Ground Water Association.

The influence of fish ponds and salinization on groundwater quality in the multi-layer coastal aquifer system in Israel

Science.gov (United States)

Tal, A.; Weinstein, Y.; Yechieli, Y.; Borisover, M.

2017-08-01

This study focuses on the impact of surface reservoirs (fish ponds) on a multi aquifer coastal system, and the relation between the aquifer and the sea. The study was conducted in an Israeli Mediterranean coastal aquifer, which includes a sandy phreatic unit and two confined calcareous sandstone units. The geological description is based on 52 wells, from which 33 samples were collected for stable isotope analysis and 25 samples for organic and inorganic parameters. Hydraulic head and chemical measurements suggest that there is an hydraulic connection between the fish ponds above the aquifer and the phreatic unit, whereas the connection with the confined units is very limited. The phreatic unit is characterized by a low concentration of oxygen and high concentrations of ammonium and phosphate, while the confined units are characterized by higher oxygen and much lower ammonium and phosphate concentrations. Organic matter fluorescence was found to be a tool to distinguish the contribution of the pond waters, whereby a pond water signature (characterized by proteinaceous (tryptophan-like) and typical humic-matter fluorescence) was found in the phreatic aquifer. The phreatic unit is also isotopically enriched, similar to pond waters, with δ18O of -1‰ and δD of -4.6‰, indicating enhanced evaporation of the pond water before infiltration, whereas there is a depleted isotopic composition in the confined units (δ18O = -4.3‰, δD = -20.4‰), which are also OM-poor. The Phreeqc model was used for quantitative calculation of the effect of pond losses on the different units. The Dissolved Inorganic Nitrogen (DIN) in the upper unit increases downstream from the ponds toward the sea, probably due to organic matter degradation, suggesting contribution of DIN from shallow groundwater flow to the sea. 87Sr/86Sr and Mg/Ca in the brackish and saline groundwater of the lower confined units increase toward seawater value, suggesting that the salinization process in the region

Baseline Geochemistry of Natural Occurring Methane and Saline Groundwater in an Area of Unconventional Shale Gas Development Through Time

Science.gov (United States)

Harkness, J.; Darrah, T.; Warner, N. R.; Whyte, C. J.; Moore, M. T.; Millot, R.; Kloppmann, W.; Jackson, R. B.; Vengosh, A.

2017-12-01

Naturally occurring methane is nearly ubiquitous in most sedimentary basins and delineating the effects of anthropogenic contamination sources from geogenic sources is a major challenge for evaluating the impact of unconventional shale gas development on water quality. This study employs a broadly integrated study of various geochemical techniques to investigate the geochemical variations of groundwater and surface water before, during, and after hydraulic fracturing.This approache combines inorganic geochemistry (major cations and anions), stable isotopes of select inorganic constituents including strontium (87Sr/86Sr), boron (δ11B), lithium (δ7Li), and carbon (δ13C-DIC), select hydrocarbon molecular (methane, ethane, propane, butane, and pentane) and isotopic tracers (δ13C-CH4, δ13C-C2H6), tritium (3H), and noble gas elemental and isotopic composition (He, Ne, Ar) to apportion natural and anthropogenic sources of natural gas and salt contaminants both before and after drilling. Methane above 1 ccSTP/L in groundwater samples awas strongly associated with elevated salinity (chloride >50 mg/L).The geochemical and isotopic analysis indicate saline groundwater originated via naturally occurring processes, presumably from the migration of deeper methane-rich brines that have interacted extensively with coal lithologies. The chemistry and gas compostion of both saline and fresh groundwater wells did not change following the installation of nearby shale-gas wells.The results of this study emphasize the value of baseline characterization of water quality in areas of fossil fuel exploration. Overall this study presents a comprehensive geochemical framework that can be used as a template for assessing the sources of elevated hydrocarbons and salts to water resources in areas potentially impacted by oil and gas development.

Calculation of electron and isotopes dose point kernels with FLUKA Monte Carlo code for dosimetry in nuclear medicine therapy.

Science.gov (United States)

Botta, F; Mairani, A; Battistoni, G; Cremonesi, M; Di Dia, A; Fassò, A; Ferrari, A; Ferrari, M; Paganelli, G; Pedroli, G; Valente, M

2011-07-01

The calculation of patient-specific dose distribution can be achieved by Monte Carlo simulations or by analytical methods. In this study, FLUKA Monte Carlo code has been considered for use in nuclear medicine dosimetry. Up to now, FLUKA has mainly been dedicated to other fields, namely high energy physics, radiation protection, and hadrontherapy. When first employing a Monte Carlo code for nuclear medicine dosimetry, its results concerning electron transport at energies typical of nuclear medicine applications need to be verified. This is commonly achieved by means of calculation of a representative parameter and comparison with reference data. Dose point kernel (DPK), quantifying the energy deposition all around a point isotropic source, is often the one. FLUKA DPKS have been calculated in both water and compact bone for monoenergetic electrons (10-3 MeV) and for beta emitting isotopes commonly used for therapy (89Sr, 90Y, 131I 153Sm, 177Lu, 186Re, and 188Re). Point isotropic sources have been simulated at the center of a water (bone) sphere, and deposed energy has been tallied in concentric shells. FLUKA outcomes have been compared to PENELOPE v.2008 results, calculated in this study as well. Moreover, in case of monoenergetic electrons in water, comparison with the data from the literature (ETRAN, GEANT4, MCNPX) has been done. Maximum percentage differences within 0.8.RCSDA and 0.9.RCSDA for monoenergetic electrons (RCSDA being the continuous slowing down approximation range) and within 0.8.X90 and 0.9.X90 for isotopes (X90 being the radius of the sphere in which 90% of the emitted energy is absorbed) have been computed, together with the average percentage difference within 0.9.RCSDA and 0.9.X90 for electrons and isotopes, respectively. Concerning monoenergetic electrons, within 0.8.RCSDA (where 90%-97% of the particle energy is deposed), FLUKA and PENELOPE agree mostly within 7%, except for 10 and 20 keV electrons (12% in water, 8.3% in bone). The

Isotope exchange reactions in hydrogen mixtures

International Nuclear Information System (INIS)

Czaplinski, W.; Gula, A.; Kravtsov, A.; Mikhailov, A.; Popov, N.

1990-12-01

The rates of isotopic exchange for the excited states of muonic hydrogen are calculated as functions of collision energy. Ground state population q 1s for different collision energies, target densities and isotope concentrations is obtained. It is shown that for principal quantum numbers n > 5 the isotopic exchange still considerably influences the value of q 1s . (author)

A Fast Numerical Method for the Calculation of the Equilibrium Isotopic Composition of a Transmutation System in an Advanced Fuel Cycle

Directory of Open Access Journals (Sweden)

F. Álvarez-Velarde

2012-01-01

Full Text Available A fast numerical method for the calculation in a zero-dimensional approach of the equilibrium isotopic composition of an iteratively used transmutation system in an advanced fuel cycle, based on the Banach fixed point theorem, is described in this paper. The method divides the fuel cycle in successive stages: fuel fabrication, storage, irradiation inside the transmutation system, cooling, reprocessing, and incorporation of the external material into the new fresh fuel. The change of the fuel isotopic composition, represented by an isotope vector, is described in a matrix formulation. The resulting matrix equations are solved using direct methods with arbitrary precision arithmetic. The method has been successfully applied to a double-strata fuel cycle with light water reactors and accelerator-driven subcritical systems. After comparison to the results of the EVOLCODE 2.0 burn-up code, the observed differences are about a few percents in the mass estimations of the main actinides.

Geochemistry and environmental isotope of groundwater from the upper Cretaceous aquifer of Orontes basin (Syria)

International Nuclear Information System (INIS)

Al-Charideh, A.

2010-03-01

Chemical and environmental isotopes have been used for studying the Upper Cretaceous aquifer systems in the Middle Orontes basin. The results indicate that the salinity of groundwater (0.2 to 2 g/l) reveals the dissolution of evaporate rocks is the main factor of high salinity especially in the Homes depression. The degree of salinity and its spaces distribution are basically related to the pattern of groundwater movement in the Upper cretaceous aquifer. The stable isotopes composition of groundwater in the Homes depression are more depleted by -2.5% and -17.0% for δ 18 O and δ 2 H respectively, than the groundwater from Hama elevation, suggested different origin and recharge time between this two groundwater groups. Estimates of their mean subsurface residence times have been constrained on the basis of 14 C D IC. The corrected ages of groundwater are recent and less to 10 thousand years in Hama uplift. However, the corrected age of groundwater in the Homs depression range between 10 to 25 thousand years indicate late Pleistocene recharge period. (author)

Determination of triazines in hemodialysis saline solutions by adsorptive stripping voltammetry after extraction in acetonitrile

Directory of Open Access Journals (Sweden)

Nascimento Paulo Cícero do

2003-01-01

Full Text Available A method for the voltammetric determination of 2-methylthio-4,6-dialkylamino-1,3,5-triazine (triazines herbicides in hemodialysis (HD saline solutions was developed. The herbicides were detected in the saline solutions at the hanging mercury drop electrode (HMDE with high sensitivities only after extraction of the analytes in acetonitrile (ACN. The salting out effect originated by the saline environment existing in the solutions enabled the extractions. The volume ratio between the saline and ACN phases was investigated in order to find the best sensitivity to detect the triazines. The speciation amongst them (ametryn, desmetryn, prometryn and terbutryn was not possible. Recoveries between 88 and 107% were calculated in spiked samples, and detection limits of 0.03 mumol L-1 were calculated for the triazines in the saline samples using this methodology.

Shape coexistence and bubble structure in Iodine isotopes

International Nuclear Information System (INIS)

Naz, Tabassum; Karim, Afaque; Ahmad, Shakeb

2017-01-01

The evolution of the shape from the spherical to the axially deformed shapes of Iodine isotopes (Z=53, N=70-80) have been investigated in the framework of self-consistent Relativistic Hartree- Bogoliubov (RHB) calculations. A nonlinear meson-nucleon coupling model represented by the NL3* parametrization of the relativistic mean-field (RMF) theory has also been used. The bulk and the microscopic properties of these nuclei have been studied. The constraint calculation has been done to obtain potential energy surface (PES). The PES curves clearly shows the shape coexistence behaviour in these isotopes. We have also obtained the neutron, proton and total density of iodine isotopes. We observe the depletion in central density which indicates the bubble structure in iodine isotopes. For which, we have calculated Depletion Fraction (D.F) which clearly states that nuclei posses bubble structure in their intrinsic states. Overall good agreement is found within the different models used and between the calculated and experimental results wherever available. (author)

Cluster decay of 218U isotope

International Nuclear Information System (INIS)

Shivakumaraswamy, G.; Umesh, T.K.

2012-01-01

The phenomenon of spontaneous emission of charged particles heavier than alpha particle and lighter than a fission fragment from radioactive nuclei without accompanied by the emission of neutrons is known as cluster radioactivity or exotic radioactivity. The process of emission of charged particles heavier than alpha particle and lighter than a fission fragment is called exotic decay or cluster decay. The phenomenon of cluster radioactivity was first predicted theoretically by Sandulescu et al in 1980. Rose and Jones made first experimental observations of 14 C emission from 223 Ra in 1984. Several cluster decay modes in trans-lead region have been experimentally observed. The half-life values for different modes of cluster decay from different isotopes of uranium have been calculated using different theoretical models such as the analytical super asymmetric model (ASAFM), Preformed cluster model (PCM) and Coulomb and Proximity potential model (CPPM) etc. Recently some semi-empirical formulae, i.e, single line of universal curve (UNIV), Universal decay law (UDL) for both alpha and cluster radioactivity have also been proposed to explain cluster decay data. The alpha decay half-life of 218-219 U isotopes has been experimentally measured in 2007. The half-life values for different cluster decay modes of 218 U isotopes have been calculated PCM model. Recently in 2011, the half-life values have also been calculated for some cluster decay modes of 222-236 U isotopes using the effective liquid drop description with the varying mass asymmetry (VMAS) shape and effective inertial coefficient. In the light of this, in the present work we have studied the cluster radioactivity of 218 U isotope. The logarithmic half-lives for few cluster decay modes from 218 U isotope have been calculated by using three different approaches, i.e, UNIV proposed by Poenaru et al in 2011, UDL proposed by Qi et al in 2009 and the CPPM model proposed by Santhosh et al in 2002. The CPPM based

Coupled geochemical/hydrogeological modelling to assess the origin of salinity at the Tono area (Japan)

International Nuclear Information System (INIS)

Guimera, Jordi; Ruiz, Eduardo; Luna, Miguel; Arcos, David; Jordana, Salvador; Saegusa, Hiromitsu

2005-01-01

Numerical models are powerful tools for the characterization of groundwater flow, especially when integrating geochemical and hydrogeological data. This paper describes modeling exercises performed in the area surrounding the Mizunami Underground Research Laboratory (MIU) Construction Site in central Japan. A particular issue being investigated at the MIU Site is the presence of saline water detected at depth in certain boreholes. The main objective of this study is to develop conceptual physical models for the origin of this salinity and to test these conceptual models using numerical modeling techniques. One scenario being investigated is that the saline fluids represent residual Miocene age seawater which has been slightly altered by water-rock interactions. It is likely that during Miocene times, seawater inundated the Tono area. This hypothesis is partially supported by carbon and oxygen isotopic data of the calcite fracture filling materials. (author)

Detecting isotopic ratio outliers

International Nuclear Information System (INIS)

Bayne, C.K.; Smith, D.H.

1985-01-01

An alternative method is proposed for improving isotopic ratio estimates. This method mathematically models pulse-count data and uses iterative reweighted Poisson regression to estimate model parameters to calculate the isotopic ratios. This computer-oriented approach provides theoretically better methods than conventional techniques to establish error limits and to identify outliers. 6 refs., 3 figs., 3 tabs

Last Glacial Maximum Salinity Reconstruction

Science.gov (United States)

Homola, K.; Spivack, A. J.

2016-12-01

It has been previously demonstrated that salinity can be reconstructed from sediment porewater. The goal of our study is to reconstruct high precision salinity during the Last Glacial Maximum (LGM). Salinity is usually determined at high precision via conductivity, which requires a larger volume of water than can be extracted from a sediment core, or via chloride titration, which yields lower than ideal precision. It has been demonstrated for water column samples that high precision density measurements can be used to determine salinity at the precision of a conductivity measurement using the equation of state of seawater. However, water column seawater has a relatively constant composition, in contrast to porewater, where variations from standard seawater composition occur. These deviations, which affect the equation of state, must be corrected for through precise measurements of each ion's concentration and knowledge of apparent partial molar density in seawater. We have developed a density-based method for determining porewater salinity that requires only 5 mL of sample, achieving density precisions of 10-6 g/mL. We have applied this method to porewater samples extracted from long cores collected along a N-S transect across the western North Atlantic (R/V Knorr cruise KN223). Density was determined to a precision of 2.3x10-6 g/mL, which translates to salinity uncertainty of 0.002 gms/kg if the effect of differences in composition is well constrained. Concentrations of anions (Cl-, and SO4-2) and cations (Na+, Mg+, Ca+2, and K+) were measured. To correct salinities at the precision required to unravel LGM Meridional Overturning Circulation, our ion precisions must be better than 0.1% for SO4-/Cl- and Mg+/Na+, and 0.4% for Ca+/Na+, and K+/Na+. Alkalinity, pH and Dissolved Inorganic Carbon of the porewater were determined to precisions better than 4% when ratioed to Cl-, and used to calculate HCO3-, and CO3-2. Apparent partial molar densities in seawater were

The procedure and results of calculations of the equilibrium isotopic composition of a demonstration subcritical molten salt reactor

Energy Technology Data Exchange (ETDEWEB)

Nevinitsa, V. A., E-mail: Neviniza-VA@nrcki.ru; Dudnikov, A. A.; Blandinskiy, V. Yu.; Balanin, A. L.; Alekseev, P. N. [National Research Centre Kurchatov Institute (Russian Federation); Titarenko, Yu. E.; Batyaev, V. F.; Pavlov, K. V.; Titarenko, A. Yu., E-mail: yuri.titarenko@itep.ru [Institute for Theoretical and Experimental Physics (Russian Federation)

2015-12-15

A subcritical molten salt reactor with an external neutron source is studied computationally as a facility for incineration and transmutation of minor actinides from spent nuclear fuel of reactors of VVER-1000 type and for producing {sup 233}U from {sup 232}Th. The reactor configuration is chosen, the requirements to be imposed on the external neutron source are formulated, and the equilibrium isotopic composition of heavy nuclides and the key parameters of the fuel cycle are calculated.

Evaluation of some soil amendments plant productivity under saline conditions using nuclear techniques

International Nuclear Information System (INIS)

Aly, E.A.K.

2004-01-01

this study was carried out in Wadi Ras Sudr (south Saini government). this location was characterized as poor soil with high salinity (wasteland). in the same time it suffers from shortage of water resources. therefore, we aimed to utilize this soil as well as the saline ground water for introducing it into production systems. the reclamation of virgin poor soil need large efforts and much research, especially plant exposure to salinity which is rapidly followed by a decrease in growth rate. the use of natural organic sources as organic fertilizers improve the growth and yields of plants, and safe the environment from pollution . organic fertilizers (Of) such as green manure (G M) or poultry manure (P M) can be used as nutrient sources for good plant growth, where the soil amendments improve the physical, chemical and biological properties of the soil. economically, the yield improvement and nutrient supply will reflect the potential use of such organic materials. also , phosphorus and/or potassium supplementation separately or in combination with O F (G M and/or P M) improved the growth of both barley and wheat plants under such adverse condition of salinity using 15 N isotope dilution technique

Isotopic depletion with Monte Carlo

International Nuclear Information System (INIS)

Martin, W.R.; Rathkopf, J.A.

1996-06-01

This work considers a method to deplete isotopes during a time- dependent Monte Carlo simulation of an evolving system. The method is based on explicitly combining a conventional estimator for the scalar flux with the analytical solutions to the isotopic depletion equations. There are no auxiliary calculations; the method is an integral part of the Monte Carlo calculation. The method eliminates negative densities and reduces the variance in the estimates for the isotope densities, compared to existing methods. Moreover, existing methods are shown to be special cases of the general method described in this work, as they can be derived by combining a high variance estimator for the scalar flux with a low-order approximation to the analytical solution to the depletion equation

Improvement of Chickpea Growth and Biological N Fixation under Water Salinity Stress

International Nuclear Information System (INIS)

Gadalla, A. M.; Galal, Y. G. M.; Hamdy, A.

2004-01-01

This work had been carried out under greenhouse conditions of IAM-Bari, aimed at evaluating the effects of water and soil salinity on growth, yield and nitrogen fixation by chickpea plants inoculated with selected Rhizobium strains. Isotope dilution approach ( 15 N) was applied for quantification of biological N fixation and portions derived from fertilizer and soil (Ndff and Ndfs, respectively). Number of pods was decreased gradually with increasing water salinity levels. High levels of salinity negatively affected shoot, root dry matter, seed yield and N accumulated in shoots and roots. A slight difference in seed N was noticed between fresh water and 9 dS/m treatments. Nitrogen derived from fertilizer by shoots was slightly increased with 3, 6 and 9 dS/m treatments, while they were notably higher than the fresh water control. More than 80% and 70% of N accumulated in shoots and seeds, respectively were derived from fixation. Portions of N 2 -fixed in shoots was decreased with the level of 3 dS/m as compared to the fresh water, then tended to increase with both 6 and 9 dS/m treatments. Stability of %Ndfa with increasing salinity was noticed with seeds-N. Soil-N came next as a fraction of nitrogen demand, where it increased with increasing water salinity levels. Under adverse conditions of salinity, the plants offered some of their N requirements from the other two N sources. Application of the suitable Rhizobium bacteria strains could be profits for both of the plant growth and soil fertility via N 2 fixation. (Authors)

Calculation of turnover rates in stable-isotope studies

International Nuclear Information System (INIS)

Wootton, R.; Ford, G.C.; Cheng, K.N.; Halliday, D.

1985-01-01

In a comparison of glucose turnover measured with 2 H-glucose and with 13 C-glucose Tserng and Kalhan used five apparently different equations and obtained conflicting answers. There is, however, no difference in principle between the use of a stable isotope as a tracer and the use of a radioactive isotope, and the rate of appearance of tracee in a steady-state system (the turnover) can therefore be shown to be proportional to the equilibrium dilution of the infused tracer. Because the sensitivity of measurement of this dilution made using a gas chromatograph-mass spectrometer is lower than that made by radioactivity measurement, the contribution to the measured turnover rate due to the infusate cannot be neglected, as it usually is in radioisotope work. A convenient calibration curve to establish this dilution is the mole ratio of the pure infusate against the area ratio for the relevant ions. Tserng and Kalhan's apparently conflicting results for glucose-turnover using 13 C-glucose as the tracer can all be shown to amount to approximately 11.6 μmol min -1 kg -1 . This value is only slightly lower (0.05 2 H-glucose as the tracer and supports the use of 13 C-glucose as an alternative. (author)

Alteration of the cementitious material under the saline environment

International Nuclear Information System (INIS)

Owada, H.; Asano, H.; Kuno, Y.; Sakamoto, H.; Shimoda, S.

2006-01-01

Leaching experiment of ordinary and fly ash mixed cement were carried out by using the artificial sea water and deionized water as leachates. The pH values of saline leachates were decreased at the lower solid/liquid ratio in comparison with the case of deionized leachates. Mg(OH) 2 and ettringite were observed only in the case of saline water. The results of the geochemical calculation with inputs of Mg(OH) 2 , ettringite and hydrotalcite well represented in the change of pH value and the mineral-composition with those of the experiment. However, in the latter stage of the fly ash mixed cement case, calculated concentrations of Si and Al of the leachate weren't consistent with the observed values. These results showed that substitution of Mg for Ca and influences of sulfate ion should be considered in the modeling of the cement alteration in the saline water case, and Al-substituted C-S-H might be considered in the alteration of fly ash mixed cement. (author)

Salinity of the Archaean oceans from analysis of fluid inclusions in quartz

Science.gov (United States)

Marty, Bernard; Avice, Guillaume; Bekaert, David V.; Broadley, Michael W.

2018-05-01

Fluids trapped in inclusions in well-characterized Archaean hydrothermal quartz crystals were analyzed by the extended argon-argon method, which permits the simultaneous measurement of chlorine and potassium concentrations. Argon and nitrogen isotopic compositions of the trapped fluids were also determined by static mass spectrometry. Fluids were extracted by stepwise crushing of quartz samples from North Pole (NW Australia) and Barberton (South Africa) 3.5-3.0-Ga-old greenstone belts. The data indicate that fluids are a mixture of a low salinity end-member, regarded as the Archaean oceanic water, and several hydrothermal end-members rich in Cl, K, N, and radiogenic parentless 40Ar. The low Cl-K end-member suggests that the salinity of the Archaean oceans was comparable to the modern one, and that the potassium content of the Archaean oceans was lower than at present by about 40%. A constant salinity of the oceans through time has important implications for the stabilization of the continental crust and for the habitability of the ancient Earth.

Large effect of irradiance on hydrogen isotope fractionation of alkenones in Emiliania huxleyi

Science.gov (United States)

van der Meer, Marcel T. J.; Benthien, Albert; French, Katherine L.; Epping, Eric; Zondervan, Ingrid; Reichart, Gert-Jan; Bijma, Jelle; Sinninghe Damsté, Jaap S.; Schouten, Stefan

2015-07-01

The hydrogen isotopic (δD) composition of long-chain alkenones produced by certain haptophyte algae has been suggested as a potential proxy for reconstructing paleo sea surface salinity. However, environmental parameters other than salinity may also affect the δD of alkenones. We investigated the impact of the level of irradiance on hydrogen isotopic fractionation of alkenones versus growth water by cultivating two strains of the cosmopolitan haptophyte Emiliania huxleyi at different light intensities. The hydrogen isotope fractionation decreased by approximately 40‰ when irradiance was increased from 15 to 200 μmol photons m-2 s-1 above which it was relatively constant. The response is likely a direct effect of photosystem I and II activity as the relationship of the fractionation factor α versus light intensity can be described by an Eilers-Peeters photosynthesis model. This irradiance effect is in agreement with published δD data of alkenones derived from suspended particulate matter collected from different depths in the photic zone of the Gulf of California and the eastern tropical North Pacific. However, haptophyte algae tend to bloom at relatively high light intensities (>500 μmol photons m-2 s-1) occurring at the sea surface, at which hydrogen isotope fractionation is relatively constant and not affected by changes in light intensity. Alkenones accumulating in the sediment are likely mostly derived from these surface water haptophyte blooms, when the largest amount of biomass is produced. Therefore, the observed irradiance effect is unlikely to affect the applicability of the hydrogen isotopic composition of sedimentary long chain alkenones as a proxy for paleosalinity.

Hydrology of marginal evaporitic basins during the Messinian Salinity Crisis: isotopic investigation of gypsum deposits

Science.gov (United States)

El Kilany, Aida; Caruso, Antonio; Dela Pierre, Francesco; Natalicchio, Marcello; Rouchy, Jean-Marie; Pierre, Catherine; Balter, Vincent; Aloisi, Giovanni

2016-04-01

The deposition of gypsum in Messinian Mediterranean marginal basins is controlled by basin restriction and the local hydrological cycle (evaporation/precipitation rates and relative importance of continental vs marine water inputs). We are using the stable isotopic composition of gypsum as a proxy of the hydrological cycle that dominated at the moment of gypsum precipitation. We studied the Messinian Caltanissetta (Sicily) and Tertiary Piedmont (north western Italy) basins where we carried out a high-resolution isotopic study of gypsum layers composing gypsum-marl cycles. These cycles are thought to be the sedimentary expression of astronomical precession cycles, lasting approximately 20 kyr, during which the marginal basins experienced a succession of arid and a wet conditions. We determined the isotopic composition of gypsum hydration water (18O and D), of the sulphate ion (34S, 18O) and of Strontium (87/86Sr), all of which are potentially affected by the hydrological cycle. In our samples, the mother water from which gypsum precipitated is considerably lighter (-4.0 micro-scale. This is an essential step in interpreting the isotopic signals of gypsum because we can expect the 18O and D composition of Messinian continental input to be not too dissimilar from that of modern meteoric waters involved in diagenetic processes.

Thermophysical properties of solid lithium hydride and its isotopic modifications

International Nuclear Information System (INIS)

Mel'nikova, T.N.

1981-01-01

The theory of the anharmonic lattice is used to calculate the thermophysical properties (thermal expansivity, lattice constant, compressibility, and elastic moduli) of all the isotopic modifications of solid lithium hydride sup(6,7)Li(H,D,T) at temperatures up to the melting point. A general analysis of isotopic effects is carried out; in particular the reverse isotopic effect in the lattice constant is explained and the isotopic effect in melting is discussed. The results of the calculations agree with available experimental data and can be used for those isotopic modifications of lithium hydride for which there exist no experimental results. (author)

Contribution of Isotopic Tools to the Numerical Simulation of the Mar del Plata Coastal Aquifer, Argentina

Energy Technology Data Exchange (ETDEWEB)

Bocanegra, E.; Martinez, D. E. [Instituto de Geologia de Costas y del Cuaternario, UNMDP (Argentina); Pool, M.; Carrera, J. [Instituto de Diagnostico Ambiental y Estudios del Agua, CSIC (Spain)

2013-07-15

Over-exploitation in the coastal aquifer in Mar del Plata, Argentina, led to a seawater intrusion process affecting groundwater by salinization. The aim of this paper is to show the contribution of isotopic techniques to generate the numerical flow and transport model of the Mar del Plata aquifer. On the basis of the hydrogeological conceptual model, a numerical model was constructed. It consists of a multilayer aquifer in the urban area with 2 layers separated by an aquitard and a monolayer aquifer in the rest of the basin. The isotopic difference recorded in groundwaters allow the identification of the origin of the recharge and the confirmation of the presence of the hydrogeological environments incorporated in the numerical model. Flow simulation reflects the evolution of piezometric heads. Chloride transport simulation represents the salinization process due to seawater intrusion and the subsequent backward movement of the interface due to the abandonment of salinized wells. The results of numerical simulation confirm the conceptual model and reproduce the impact of the adopted management strategies. (author)

Assessment of groundwater pollution from ash ponds using stable and unstable isotopes around the Koradi and Khaperkheda thermal power plants (Maharashtra, India)

Energy Technology Data Exchange (ETDEWEB)

Voltaggio, M.; Spadoni, M. [CNR — Istituto di Geologia Ambientale e Geoingegneria, Via Salaria km. 29.300, 00010 Montelibretti, Roma (Italy); Sacchi, E. [Dept. of Earth and Environmental Sciences, University of Pavia and CNR-IGG, Via Ferrata 1, 27100 Pavia (Italy); Sanam, R.; Pujari, P.R.; Labhasetwar, P.K. [CSIR-National Environmental Engineering Research Institute, Nehru Marg, Nagpur 440020 (India)

2015-06-15

The impact on local water resources due to fly ash produced in the Koradi and Khaperkheda thermal power plants (district of Nagpur, Maharashtra — India) and disposed in large ponds at the surface was assessed through the study of environmental variation of ratios of stable and unstable isotopes. Analyses of oxygen and hydrogen isotopes suggest scarce interaction between the water temporarily stored in the ponds and the groundwater in the study area. Data also highlight that the high salinity of groundwater measured in the polluted wells is not due to evaporation, but to subsequent infiltration of stream waters draining from the ponds to the local aquifer. {sup 87}Sr/{sup 86}Sr values, when associated with Sr/Ca ratios, demonstrate the dominant role of waste waters coming from tens of brick kilns surrounding the pond sulfate pollution. Uranium isotopic analyses clearly show evidence of the interaction between groundwater and aquifer rocks, and confirm again the low influence of ash ponds. A new conceptual model based on the study of the isotopes of radium is also proposed and used to estimate residence times of groundwater in the area. This model highlights that high salinity cannot be in any case attributed to a prolonged water–rock interaction, but is due to the influence of untreated waste water of domestic or brick kiln origin on the shallow and vulnerable aquifers. - Highlights: • Ash ponds have wide environmental and social impact in India. • Isotope ratios can be used as tracers for possible pollution of groundwater. • Isotopes of O, H, Sr, U and Ra have been used to investigate the area of Koradi. • Salinity of groundwater is not due to fly ash but linked to local brick kilns. • A model for the residence time of water based on Ra isotopes is described.

The integrated impacts of natural processes and human activities on the origin and processes of groundwater salinization in the coastal aquifers of Beihai, Southern China

Science.gov (United States)

Li, Q.; Zhan, Y., , Dr; Chen, W. Ms; Yu, S., , Dr

2017-12-01

Salinization in coastal aquifers usually is the results of contamination related to both seawater intrusion and water-rock interaction. The chemical and isotopic methods were combined to identify the origin and processes of groundwater salinization in Daguansha area of Beihai. The concentrations of the major ions that dominate in sea water (Cl-, Na+, Ca2+, Mg2+ and SO2- 4), as well as the isotopic ratios (2H, 18O, 87Sr/86Sr and 13C) suggest that the salinization occurring in the aquifer water of the coastal plain is related to seawater and the prevailing hydrochemical processes are evaporation, mixing, dissolution and ion exchange. For the unconfined aquifer, groundwater salinization occurred in parts of the area, which is significantly influenced by the land-based sea farming. The integrated impacts of seawater intrusion from the Beibuwan Gulf and infiltration of seawater from the culture ponds is identified in the confined aquifer I at site BBW2. In consequence, the leakage from this polluted aquifer causes the salinization of groundwater in the confined aquifer II. At site BBW3, the confined aquifer I and lower confined aquifer II are remarkably contaminated by seawater intrusion. The weak connectivity with upper aquifers and seaward movement of freshwater prevents saltwater from encroaching the confined aquifer III. Above all, understanding of the origin and processes of groundwater salinization will provide essential information for sustainable planning and management of groundwater resources in this region.

Groundwater dependent pools in seasonal and permanent streams in the Clare Valley of South Australia

Directory of Open Access Journals (Sweden)

Erick Bestland

2017-02-01

In this Mediterranean climate with cool wet winters and dry hot summers strong salinity changes (up to 2.5 times due to seasonal cycles of wetting and drying were observed in surface water. Oxygen and hydrogen isotope values from pool sites showed strong evaporative enrichment during the dry season with up to 50% net evaporation calculated. Water isotopes from groundwater, however, cluster at the depleted end of the local meteoric water line and most do not show change despite significant seasonal salinity changes. Strontium isotope values and concentrations from the pools over the one year period do not define a mixing relationship. Instead, most pool sites have unchanging strontium isotope values despite the large seasonal change in salinity indicating strong evaporation of groundwater fed pools during this drought year.

Variability in copepod trophic levels and feeding selectivity based on stable isotope analysis in Gwangyang Bay of the southern coast of the Korean Peninsula

Science.gov (United States)

Chen, Mianrun; Kim, Dongyoung; Liu, Hongbin; Kang, Chang-Keun

2018-04-01

Trophic preference (i.e., food resources and trophic levels) of different copepod groups was assessed along a salinity gradient in the temperate estuarine Gwangyang Bay of Korea, based on seasonal investigation of taxonomic results in 2015 and stable isotope analysis incorporating multiple linear regression models. The δ13C and δ15N values of copepods in the bay displayed significant spatial heterogeneity as well as seasonal variations, which were indicated by their significant relationships with salinity and temperature, respectively. Both spatial and temporal variations reflected those in isotopic values of food sources. The major calanoid groups (marine calanoids and brackish water calanoids) had a mean trophic level of 2.2 relative to nanoplankton as the basal food source, similar to the bulk copepod assemblage; however, they had dissimilar food sources based on the different δ13C values. Calanoid isotopic values indicated a mixture of different genera including species with high δ15N values (e.g., Labidocera, Sinocalanus, and Tortanus), moderate values (Calanus sinicus, Centropages, Paracalanus, and Acartia), and relatively low δ15N values (Eurytemora pacifica and Pseudodiaptomus). Feeding preferences of different copepods probably explain these seasonal and spatial patterns of the community trophic niche. Bayesian mixing model calculations based on source materials of two size fractions of particulate organic matter (nanoplankton at simple energy flow of the planktonic food web of Gwangyang Bay: from primary producers (nanoplankton) and a mixture of primary producers and herbivores (microplankton) through omnivores (Acartia, Calanus, Centropages, and Paracalanus) and detritivores (Pseudodiaptomus, Eurytemora, and harpacticoids) to carnivores (Corycaeus, Tortanus, Labidocera, and Sinocalanus).

Three-dimensional calculations of neutron streaming in the beam tubes of the ORNL HFIR [High Flux Isotope Reactor] Reactor

International Nuclear Information System (INIS)

Childs, R.L.; Rhoades, W.A.; Williams, L.R.

1988-01-01

The streaming of neutrons through the beam tubes in High Flux Isotope Reactor at Oak Ridge National Laboratory has resulted in a reduction of the fracture toughness of the reactor vessel. As a result, an evaluation of vessel integrity was undertaken in order to determine if the reactor can be operated again. As a part of this evaluation, three-dimensional neutron transport calculations were performed to obtain fluxes at points of interest in the wall of the vessel. By comparing the calculated and measured activation of dosimetry specimens from the vessel surveillance program, it was determined that the calculated flux shape was satisfactory to transpose the surveillance data to the locations in the vessel. A bias factor was applied to correct for the average C/E ratio of 0.69. 8 refs., 7 figs., 3 tabs

Calculation of Plutonium content in RSG-GAS spent fuel using IAFUEL computer code

International Nuclear Information System (INIS)

Mochamad-Imron

2003-01-01

It has been calculated the contain of isotopes Pu-239, Pu-240, Pu-241, and isotope Pu-242 in MTR reactor fuel types which have U-235 contain about 250 gram. The calculation was performed in three steps. The first step is to determine the library of calculation output of BOC (Beginning of Cycle). The second step is to determine the core isotope density, the weight of plutonium for one core, and one fuel isotope density. The third step is to calculate weight of plutonium in gram. All calculation is performed by IAFUEL computer code. The calculation was produced content of each Pu isotopes were Pu-239 is 6.7666 gr, Pu-240 is 1.4628 gr, Pu-241 is 0.52951 gr, and Pu-242 is 0.068952 gr

Using Of Isotopes In Hydrology; Izotoplarin Hidrolojide Kullanilmasi

Energy Technology Data Exchange (ETDEWEB)

Cifter, C; Sayin, M [DSI, Technical Research and Quality Control Department, Ankara (Turkey)

2002-07-01

Current estimates are that the Earth's hydrosphere contains a huge amount of water about 1400 million cubic kilometers. However, 97.5 percent of this amount are saline waters and only 2.5 percent is fresh water. By 2025, world population is expected to be 8 billion. Quantity of the renewable water resources in Turkey has decreased due to urbanization, industrialization and population with each passing day . However quality of water resources in Turkey is affected by land use practice such as cultivation with accompanying application of large quantities of fertilizers and pesticides, ground water salutation, waste water. In this respect, new research methods were eagerly sought by researcher for developing water resources due to the rising industrial developing and growing of population. Isotope techniques provide invaluable information on the sources, movement and quantity of water in different environments. The State Hydraulic Works (DSI), Technical Research and Quality Control Department has used isotope techniques together with begin ing isotope study over the world.

Some considerations of ''cold fusion'' including the calculation of fusion rates in molecules of hydrogen isotopes

International Nuclear Information System (INIS)

Cowley, S.C.; Kulsrud, R.M.

1989-11-01

We calculate the fusion reaction rates in molecules of hydrogen isotopes. The rates are calculated analytically (for the first time) as an asymptotic expansion in the ratio of the electron mass to the reduced mass of the nucleii. The fusion rates of the P-D, D-D, and D-T reactions are given for a variable electron mass by a simple analytic formula. However, we do not know any mechanism by which a sufficiently localized electron in solid can have an 'effective mass' large enough to explain the result of Fleischman and Pons (FP). This calculation indicates that P-D rates should exceed D-D rates for D-D fusion rates less than approximately 10 -23 per molecule per second. The D-D fusion rate is enhanced by a factor of 10 5 at 10,000 degree K if the excited vibrational states are populated with a Boltzmann distribution and the rotational excitations suppressed. The suggestion that experimental results could be explained by bombardment of cold deuterons by kilovolt deuterons is shown to be an unlikely from an energetic point of view. 12 refs., 3 figs., 1 tab

Chlorine isotopic geochemistry of salt lakes in the Qaidam Basin, China

Digital Repository Service at National Institute of Oceanography (India)

Liu, W.G.; Xiao, Y.K.; Wang, Q.Z.; Qi, H.P.; Wang, Y.H.; Zhou, Y.M.; Shirodkar, P.V.

*Cl+ ion. Int. J. Mass Spectrom. Ion Process., 116: crysatallization of saline minerals in salt lake. J. Salt Lake 183-192. Sci., 2: 35-40 (in Chinese). Xiao, Y.K., Sun, D.P., Wang, Y.H., Qi, H.P. and Jin, L., 1992. Boron isotopic compositions of brine..., sediments, and source water in Da Qaidam Lake, Qinghai, China. Geochim. Cos- mochim. Acta, 56: 1.561-1568. Xiao, Y.K., Jin, L., Liu. W.G., Qi, H.P., Wang, W.H. and Sun, D.P., 1994a. The isotopic compositions of chlorine in Da Qaidam Lake. Chin. Sci...

ICT: isotope correction toolbox.

Science.gov (United States)

Jungreuthmayer, Christian; Neubauer, Stefan; Mairinger, Teresa; Zanghellini, Jürgen; Hann, Stephan

2016-01-01

Isotope tracer experiments are an invaluable technique to analyze and study the metabolism of biological systems. However, isotope labeling experiments are often affected by naturally abundant isotopes especially in cases where mass spectrometric methods make use of derivatization. The correction of these additive interferences--in particular for complex isotopic systems--is numerically challenging and still an emerging field of research. When positional information is generated via collision-induced dissociation, even more complex calculations for isotopic interference correction are necessary. So far, no freely available tools can handle tandem mass spectrometry data. We present isotope correction toolbox, a program that corrects tandem mass isotopomer data from tandem mass spectrometry experiments. Isotope correction toolbox is written in the multi-platform programming language Perl and, therefore, can be used on all commonly available computer platforms. Source code and documentation can be freely obtained under the Artistic License or the GNU General Public License from: https://github.com/jungreuc/isotope_correction_toolbox/ {christian.jungreuthmayer@boku.ac.at,juergen.zanghellini@boku.ac.at} Supplementary data are available at Bioinformatics online. © The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Rate of radiocarbon retention onto calcite by isotope exchange

Energy Technology Data Exchange (ETDEWEB)

Lempinen, Janne; Lehto, Jukka [Helsinki Univ. (Finland). Lab. of Radiochemistry

2016-11-01

Radiocarbon ({sup 14}C) is a top priority class radionuclide associated with the long-term safety of spent nuclear fuel disposal. Dissolved inorganic radiocarbon can be retained in bedrock via isotope exchange with calcite (CaCO{sub 3}) at solubility equilibrium with groundwater. In the present study, the rate of the isotope exchange process was investigated on synthetic calcite using batch experiments. Experiments were performed in solutions with a calcium concentration of 0.0002-0.1 M, including two synthetic reference groundwaters. The radiocarbon activity in the solutions decreased exponentially as a function of time, thus following first-order kinetics. The rate of isotope exchange was quantified from an exponential fit to the activity data over time. The rate of radiocarbon retention increased as a function of the calcium activity. The isotope exchange half-life was only 4.3 days at calcium ion activities over 0.01. This half-life is very much shorter than the half-life of {sup 14}C or the time scale of groundwater movements; consequently calcite can effectively retain radiocarbon from brackish and saline groundwaters.

Rate of radiocarbon retention onto calcite by isotope exchange

International Nuclear Information System (INIS)

Lempinen, Janne; Lehto, Jukka

2016-01-01

Radiocarbon ( 14 C) is a top priority class radionuclide associated with the long-term safety of spent nuclear fuel disposal. Dissolved inorganic radiocarbon can be retained in bedrock via isotope exchange with calcite (CaCO 3 ) at solubility equilibrium with groundwater. In the present study, the rate of the isotope exchange process was investigated on synthetic calcite using batch experiments. Experiments were performed in solutions with a calcium concentration of 0.0002-0.1 M, including two synthetic reference groundwaters. The radiocarbon activity in the solutions decreased exponentially as a function of time, thus following first-order kinetics. The rate of isotope exchange was quantified from an exponential fit to the activity data over time. The rate of radiocarbon retention increased as a function of the calcium activity. The isotope exchange half-life was only 4.3 days at calcium ion activities over 0.01. This half-life is very much shorter than the half-life of 14 C or the time scale of groundwater movements; consequently calcite can effectively retain radiocarbon from brackish and saline groundwaters.

A kinematic-based methodology for radiological protection: Runoff analysis to calculate the effective dose for internal exposure caused by ingestion of radioactive isotopes

Science.gov (United States)

Sasaki, Syota; Yamada, Tadashi; Yamada, Tomohito J.

2014-05-01

We aim to propose a kinematic-based methodology similar with runoff analysis for readily understandable radiological protection. A merit of this methodology is to produce sufficiently accurate effective doses by basic analysis. The great earthquake attacked the north-east area in Japan on March 11, 2011. The system of electrical facilities to control Fukushima Daiichi nuclear power plant was completely destroyed by the following tsunamis. From the damaged reactor containment vessels, an amount of radioactive isotopes had leaked and been diffused in the vicinity of the plant. Radiological internal exposure caused by ingestion of food containing radioactive isotopes has become an issue of great interest to the public, and has caused excessive anxiety because of a deficiency of fundamental knowledge concerning radioactivity. Concentrations of radioactivity in the human body and internal exposure have been studied extensively. Previous radiologic studies, for example, studies by International Commission on Radiological Protection(ICRP), employ a large-scale computational simulation including actual mechanism of metabolism in the human body. While computational simulation is a standard method for calculating exposure doses among radiology specialists, these methods, although exact, are too difficult for non-specialists to grasp the whole image owing to the sophistication. In this study, the human body is treated as a vessel. The number of radioactive atoms in the human body can be described by an equation of continuity, which is the only governing equation. Half-life, the period of time required for the amount of a substance decreases by half, is only parameter to calculate the number of radioactive isotopes in the human body. Half-life depends only on the kinds of nuclides, there are no arbitrary parameters. It is known that the number of radioactive isotopes decrease exponentially by radioactive decay (physical outflow). It is also known that radioactive isotopes

Isotope techniques in water resources development and management. Proceedings

International Nuclear Information System (INIS)

1999-01-01

The 10th International Symposium on Isotope Techniques in Water Resources Development and Management was organized by the International Atomic Energy Agency in co-operation with UNESCO, WMO and International Association of Hydrological Sciences and was held at IAEA Headquarters, Vienna, during 10-14 May 1999. The symposium provided an international forum for assessing the status and recent advances in isotope applications to water resources and an exchange of information on the following main themes: processes at the interface between the atmosphere and hydrosphere; investigations in surface waters and groundwaters: their origin, dynamics, interrelations; problems and techniques for investigating sedimentation; water resources issues: pollution, source and transport of contaminants, salinization, water-rock interaction and processes in geothermal systems; isotope data interpretation and evaluation methodologies: modelling approaches. The proceedings contain the 46 papers presented and extended synopses of poster presentations; each of them was indexed individually

Barium isotopes in cold-water corals

Science.gov (United States)

Hemsing, Freya; Hsieh, Yu-Te; Bridgestock, Luke; Spooner, Peter T.; Robinson, Laura F.; Frank, Norbert; Henderson, Gideon M.

2018-06-01

Recent studies have introduced stable Ba isotopes (δ 138 / 134Ba) as a novel tracer for ocean processes. Ba isotopes could potentially provide insight into the oceanic Ba cycle, the ocean's biological pump, water-mass provenance in the deep ocean, changes in activity of hydrothermal vents, and land-sea interactions including tracing riverine inputs. Here, we show that aragonite skeletons of various colonial and solitary cold-water coral (CWC) taxa record the seawater (SW) Ba isotope composition. Thirty-six corals of eight different taxa from three oceanic regions were analysed and compared to δ 138 / 134Ba measurements of co-located seawater samples. Sites were chosen to cover a wide range of temperature, salinity, Ba concentrations and Ba isotope compositions. Seawater samples at the three sites exhibit the well-established anti-correlation between Ba concentration and δ 138 / 134Ba. Furthermore, our data set suggests that Ba/Ca values in CWCs are linearly correlated with dissolved [Ba] in ambient seawater, with an average partition coefficient of DCWC/SW = 1.8 ± 0.4 (2SD). The mean isotope fractionation of Ba between seawater and CWCs Δ138/134BaCWC-SW is -0.21 ± 0.08‰ (2SD), indicating that CWC aragonite preferentially incorporates the lighter isotopes. This fractionation likely does not depend on temperature or other environmental variables, suggesting that aragonite CWCs could be used to trace the Ba isotope composition in ambient seawater. Coupled [Ba] and δ 138 / 134Ba analysis on fossil CWCs has the potential to provide new information about past changes in the local and global relationship between [Ba] and δ 138 / 134Ba and hence about the operation of the past global oceanic Ba cycle in different climate regimes.

Isotope effects on chemical equilibria

International Nuclear Information System (INIS)

Golding, P.D.

1974-01-01

The thermodynamic equilibrium constants of three deuterated substituted acetic acids are reported. The calculation of secondary isotope effects of the second kind for the three isotopic acid pairs has been accomplished by the appropriate comparison of thermodynamic equilibrium constants, and by the comparison of isotopic slopes. The effect of substituent variation on the isotope effects reported here disqualifies the simple inductive model as a legitimate description of secondary isotope effects of the second kind. The correlation of diminishing isotope effect per deuterium atom with increasing acidity is also invalidated by the present results. The syntheses of 9-thia-9,10-dihydrophenanthrene-9-oxide and thioxanthene-10-oxide are described. These compounds have been partially deuterated at their respective methylene positions. Spectral evidence indicates stereoselectivity of the methylene protons in the exchange reactions of both compounds. (author)

Calculation of absorbed dose for skin contamination imparted by beta radiation through the VARSKIN modified code for 122 interesting isotopes for nuclear medicine, nuclear power plants and research

International Nuclear Information System (INIS)

Alvarez R, J.T.

1991-01-01

In this work the implementation of a modification of the VARSKIN code for calculation of absorbed dose for contamination in skin imparted by external radiation fields generated by Beta emitting is presented. The modification consists on the inclusion of 47 isotopes of interest even Nuclear Plants for the dose evaluation in skin generated by 'hot particles'. The approach for to add these isotopes is the correlation parameter F and the average energy of the Beta particle, with relationship to those 75 isotopes of the original code. The methodology of the dose calculation of the VARSKIN code is based on the interpolation, (and integration of the interest geometries: punctual or plane sources), of the distribution functions scaled doses in water for beta and electrons punctual sources, tabulated by Berger. Finally a brief discussion of the results for their interpretation and use with purposes of radiological protection (dose insurance in relation to the considered biological effects) is presented

A method of uranium isotopes concentration analysis

International Nuclear Information System (INIS)

Lin Yuangen; Jiang Meng; Wu Changli; Duan Zhanyuan; Guo Chunying

2010-01-01

A basic method of uranium isotopes concentration is described in this paper. The iteration method is used to calculate the relative efficiency curve, by analyzing the characteristic γ energy spectrum of 235 U, 232 U and the daughter nuclide of 238 U, then the relative activity can be calculated, at last the uranium isotopes concentration can be worked out, and the result is validated by the experimentation. (authors)

Charge distributions of barium isotopes from muonic X-rays

International Nuclear Information System (INIS)

Shera, E.B.; Wohlfahrt, H.D.; Hoehn, M.V.; Tanaka, Y.

1982-01-01

The results of a muonic X-ray study of the charge radii of stable barium isotopes are presented and compared with optical isotope shifts. The isotope shifts Δ 2 > of a wide range of barium isotopes are found to be in good agreement with the droplet model and with IBA calculations. (orig.)

Groundwater salinity in coastal aquifer of Karachi, Pakistan

International Nuclear Information System (INIS)

Mashiatullah, A.; Qureshi, R.M.; Ahmad, E.; Tasneem, M.A.; Sajjad, M.I.; Khan, H.A.

2002-01-01

Potable groundwater salinity has become a problem of great concern in the Karachi Metropolis, which is not only the most populous and biggest industrial base but also the largest coastal dwelling of Pakistan. Stable isotope techniques [O/sup 18/ content of Oxygen in the water molecular and C/sup 13/ content of the Total Dissolved Inorganic Carbon (TDIC)] have been used, in conjunction with physiochemical tools (temperature, dissolved oxygen, pH, redox electrical conductivity, salinity), to examine the quality of potable water and the source of salinity. Surface water samples (12 No.) were collected from polluted streams, namely: Layeri River, Malir River; Hub River/Hub Lake and the Indus River. Shallow groundwater samples (7 No. ) were collected from operating dug wells. Relatively deep groundwater samples (12 No.) were collected from operating dug wells, relatively deep groundwater samples (12 No.) were collected from pumping wells/tube-wells. Physicochemical analysis of water samples was completed in the field. In the laboratory, water samples were analyzed for O/sup 18/ content of oxygen in the water molecule and C/sup 13/ content of the TDIC, using specific gas extraction systems and a modified GD-150 gas source mass spectrometer. It is concluded from this preliminary investigation that the potable aquifer system in coastal Karachi hosts a mixture of precipitation (rainwater only) from hinterlands, trapped seawater in relatively deep aquifer system, as well as intruded seawater under natural infiltration conditions and/or induced recharge conditions (in shallow aquifers). (author)

Stable isotope and hydrogeochemical studies of Beaver Lake and Lake Radok, MacRobertson Land, East Antarctica

International Nuclear Information System (INIS)

Wand, U.; Hermichen, W.D.; Hoefling, R.; Muehle, K.

1987-01-01

Beaver Lake and Lake Radok, the largest known epishelf and the deepest freshwater lake on the Antarctic continent, respectively, were isotopically (δ 2 H, δ 18 O) and hydrogeochemically studied. Lake Radok is an isothermal and non-stratified, i.e. homogeneous water body, while Beaver Lake is stratified with respect to temperature, salinity and isotopic composition. The results for the latter attest to freshwater (derived from snow and glacier melt) overlying seawater. (author)

Stable isotope and hydrogeochemical studies of Beaver Lake and Radok Lake, MacRobertson Land, East Antarctica

International Nuclear Information System (INIS)

Wand, U.; Hermichen, W.D.

1988-01-01

Beaver Lake and Radok Lake, the largest known epishelf lake and the deepest freshwater lake on the Antarctic continent, respectively, were isotopically (δ 2 H, δ 18 O) and hydrogeochemically studied. Radok Lake is an isothermal and nonstratified, i.e. homogeneous water body, while Beaver Lake is stratified with respect to temperature, salinity and isotopic composition. The results for the latter attest to freshwater (derived from snow and glacier melt) overlying seawater. (author)

C isotope fractionation during heterotrophic activity driven carbonate precipitation

Science.gov (United States)

Balci, Nurgul; Demirel, Cansu

2016-04-01

Stable carbon isotopic fractionation during carbonate precipitation induced by environmentally enriched heterotrophic halophilic microorganims was experimentally investigated under various salinity (% 4.5, %8, %15) conditions at 30 °C. Halophilic heterotrophic microorganims were enriched from a hypersaline Lake Acigöl located in SW Turkey (Balci et al.,2015) and later used for the precipitation experiments (solid and liquid medium). The carbonate precipitates had relatively high δ13C values (-4.3 to -16.9 ‰) compared to the δ13C values of the organic compounds that ranged from -27.5 to -25.4 ‰. At salinity of 4.5 % δ13C values of carbonate ranged from -4.9 ‰ to -10.9 ‰ with a 13C-enrichment factor of +20 to +16 ‰ higher than the δ13C values of the associated DOC (-27.5) . At salinity 8 % δ13C values of carbonate ranged from -16.3 ‰ to -11.7 ‰ with a 13C-enrichment factor of+11.3 to+15.9 ‰ higher than the δ13C values of the associated DOC. The respected values for 15 % salinity ranged from -12.3 ‰ to -9.7 ‰ with a 13C-enrichment factor of +15.2 to+16.8 ‰ higher than the δ13C values of the associated DOC. The carbonate precipitates produced in the solid medium are more enriched in 13C relative to liquid culture experiments. These results suggest that the carbon in the solid was derived from both the bacterial oxidation of organic compounds in the medium and from the atmospheric CO2. A solid medium used in the experiments may have suppressed convective and advective mass transport favouring diffusion-controlled system. This determination suggests that the rate and equilibration of CO2 exchange with the atmosphere is the major control on C isotope composition of carbonate minerals precipitated in the experiments. Key words: Lake Acıgöl, halophilic bacteria, carbonate biomineralization, C isotopes References Nurgul Balci, Meryem Menekşe, Nevin Gül Karagüler, M. Şeref Sönmez,Patrick Meister 2015.Reproducing authigenic carbonate

The use of isotope techniques to investigate saltwater intruded aquifers in the Philippines

International Nuclear Information System (INIS)

Peralta, G.L.

1988-01-01

Studies in Metro Manila area have identified inland bodies of saline water which have been called ''connate water''. It has been refered to in literature as saline water occurring inland at a range of depths, in close association with freshwater. The relationships between these various bodies of saline water are not clear and for groundwater development planning it would be useful to determine whether the inland cases are a series of small isolated residual bodies from the last marine transgression or parts of a large continuous saline body. Furthermore the origin and mechanism of natural groundwater recharges are often not clear from the chemical and hydrogeological data as in the island of Cebu. In these circumstances it was recommended that useful planning data be obtained from a study of the concentrations of natural isotopes in the groundwater, particularly in the areas of Manila, Cebu and Bulacan-Pampanga. (author)

Broadband non-selective excitation of plutonium isotopes for isotope ratio measurements in resonance ionization mass spectrometry: a theoretical study.

Science.gov (United States)

Sankari, M

2012-10-15

Making isotope ratio measurements with minimum isotope bias has always been a challenging task to mass spectrometrists, especially for the specific case of plutonium, owing to the strategic importance of the element. In order to use resonance ionization mass spectrometry (RIMS) as a tool for isotope ratio measurements, optimization of the various laser parameters and other atomic and system parameters is critical to minimize isotopic biases. Broadband simultaneous non-selective excitation of the isotopes of plutonium in the triple resonance excitation scheme with λ(1) = 420.77 nm, λ(2) = 847.28 nm, and λ(3) = 767.53 nm based on density matrix formalism has been theoretically computed for the determination of isotope ratios. The effects of the various laser parameters and other factors such as the atomization temperature and the dimensions of the atomic beam on the estimation of isotope ratios were studied. The effects of Doppler broadening, and time-dependent excitation parameters such as Rabi frequencies, ionization rate and the effect of non-Lorenztian lineshape have all been incorporated. The average laser powers and bandwidths for the three-excitation steps were evaluated for non-selective excitation. The laser intensity required to saturate the three-excitation steps were studied. The two-dimensional lineshape contour and its features were investigated, while the reversal of peak asymmetry of two-step and two-photon excitation peaks under these conditions is discussed. Optimized powers for the non-selective ionization of the three transitions were calculated as 545 mW, 150 mW and 545 mW and the laser bandwidth for all the three steps was ~20 GHz. The isotopic bias between the resonant and off-resonant isotope under the optimized conditions was no more than 9%, which is better than an earlier reported value. These optimized laser power and bandwidth conditions are better than in the earlier experimental work since these comprehensive calculations yield

Isotope geochemistry of water in Gulf Coast Salt Domes

International Nuclear Information System (INIS)

Knauth, L.P.; Kumar, M.B.; Martinez, J.D.

1980-01-01

Water found as active leaks and isolated pools in the Weeks Island, Jefferson Island, and Belle Isle salt mines of south Louisiana has delta 18 O values ranging from -4 to +11.5% 0 and deltaD values from -2.3 to -53% 0 . One sample from Weeks Island and one from Jefferson Island are isotopically similar to local surface waters and are clearly of meteoric origin. All other samples are too enriched in 18 O to be meteoric waters. In the Weeks Island mine the isotopic data define a linear array given by deltaD=3.0delta 18 O-40.1. Active leaks define the positive end of this array. Isolated pools are interpreted as inactive leaks with initial delta 18 O and deltaD values of +9.1 +- 0.5% 0 and -11% 0 +- 7% 0 , which have subsequently exchanged with water vapor in the mine air to produce the linear array of delta values. The water derived from active leaks in these three mines is too enriched in 18 O and too depleted in D to be connate ocean water or evaporite connate water trapped in the salt. Isotopic composition of water derived from the dehydration of gypsum is probably dissimilar to that of the active leaks. It is unlikely that the water has originated from the dehydration of gypsum. It is also unlikely that isotopic exchange with anhydrite is responsible for observed 18 O enrichments. Nonmeteroric water from the active leaks displays the type of 18 O enrichments characteristic of saline formation waters, where water exchanges isotopically with calcite and clay minerals. It is concluded that the nonmeteoric waters are formation waters which have become incorporated in the salt. From the observed 18 O enrichment it is calculated that formation waters were incorporated during diapiric rise of the salt at a depth of 3--4 km and have been trapped within the salt for 10--13 m.y. Large volumes of salt within salt domes are not naturally penetrated by meteoric groundwaters but can contain limited amounts of trapped formation water

Effect of spatial variation on salinity tolerance of macroinvertebrates in Eastern Australia and implications for ecosystem protection trigger values

International Nuclear Information System (INIS)

Dunlop, Jason E.; Horrigan, Nelli; McGregor, Glenn; Kefford, Ben J.; Choy, Satish; Prasad, Rajesh

2008-01-01

Salinisation of freshwater has been identified as a serious environmental issue in Australia and around the world. Protective concentrations (trigger values) for salinity can be used to manage salinity impacts, though require locally relevant salinity tolerance information. 72-h acute salinity tolerance values were determined for 102 macroinvertebrates collected from 11 locations in four biologically distinct freshwater bio-regions in Northeast Australia and compared with sensitivities observed in Southeast Australia. The salinity tolerance of individual taxa was consistent across Northeast Australia and between Northeast and Southeast Australia. However, two distinct communities were identified in Northeast Australia using distributions of the acute tolerance values and a calculated index of salinity sensitivity. Salinity trigger values should therefore be representative of local or regionally relevant communities and may be adequately calculated using sensitivity values from throughout Eastern Australia. The results presented provide a basis for assessing salinity risk and determining trigger values for salinity in freshwater ecosystems at local and regional scales in Eastern Australia. - Salinity tolerance of macroinvertebrate communities vary in Eastern Australia hence water quality guidelines should be developed at a local or regional scale

Isotopic analysis of uranium by thermoionic mass spectrometry

International Nuclear Information System (INIS)

Moraes, N.M.P. de.

1979-01-01

Uranium isotopic ratio measurements by thermoionic spectrometry are presented. Emphasis is given upon the investigation of the parameters that directly affect the precision and accuracy of the results. Optimized procedures, namely, chemical processing, sample loading on the filaments, vaporization, ionization and measurements of ionic currents, are established. Adequate statistical analysis of the data for the calculation of the internal and external variances and mean standard deviation are presented. These procedures are applied to natural and NBS isotopic standard uranium samples. The results obtained agree with the certified values within specified limits. 235 U/ 238 U isotopic ratios values determined for NBS-U500, and a series of standard samples with variable isotopic compositon, are used to calculate mass discrimination factor [pt

Stable isotope evidence for dietary overlap between alien and native gastropods in coastal lakes of northern KwaZulu-Natal, South Africa.

Directory of Open Access Journals (Sweden)

Nelson A F Miranda

Full Text Available Tarebia granifera (Lamarck, 1822 is originally from South-East Asia, but has been introduced and become invasive in many tropical and subtropical parts of the world. In South Africa, T. granifera is rapidly invading an increasing number of coastal lakes and estuaries, often reaching very high population densities and dominating shallow water benthic invertebrate assemblages. An assessment of the feeding dynamics of T. granifera has raised questions about potential ecological impacts, specifically in terms of its dietary overlap with native gastropods.A stable isotope mixing model was used together with gut content analysis to estimate the diet of T. granifera and native gastropod populations in three different coastal lakes. Population density, available biomass of food and salinity were measured along transects placed over T. granifera patches. An index of isotopic (stable isotopes dietary overlap (IDO, % aided in interpreting interactions between gastropods. The diet of T. granifera was variable, including contributions from microphytobenthos, filamentous algae (Cladophora sp., detritus and sedimentary organic matter. IDO was significant (>60% between T. granifera and each of the following gastropods: Haminoea natalensis (Krauss, 1848, Bulinus natalensis (Küster, 1841 and Melanoides tuberculata (Müller, 1774. However, food did not appear to be limiting. Salinity influenced gastropod spatial overlap. Tarebia granifera may only displace native gastropods, such as Assiminea cf. ovata (Krauss, 1848, under salinity conditions below 20. Ecosystem-level impacts are also discussed.The generalist diet of T. granifera may certainly contribute to its successful establishment. However, although competition for resources may take place under certain salinity conditions and if food is limiting, there appear to be other mechanisms at work, through which T. granifera displaces native gastropods. Complementary stable isotope and gut content analysis can

Spectroscopic and Quantum Mechanical Calculation Study of the Effect of Isotopic Substitution on NIR Spectra of Methanol.

Science.gov (United States)

Grabska, Justyna; Czarnecki, Mirosław A; Beć, Krzysztof B; Ozaki, Yukihiro

2017-10-19

In this work, we studied methanol and its deuterated derivatives (CH 3 OH, CH 3 OD, CD 3 OH, CD 3 OD) by NIR spectroscopy and anharmonic quantum chemical calculations. Vibrational bands corresponding to up to three quanta transitions (first and second overtones, binary and ternary combination modes) were predicted by the use of the VPT2 route. The accuracy of prediction of NIR modes was evaluated through density functional theory (DFT) with selected density functionals and basis sets. On the basis of the theoretical NIR spectra, detailed band assignments for all studied molecules were proposed. It was found that the pattern of bands in NIR spectra of deuterated methanols can be used for identification of isotopically equalized forms. Calculations of NIR spectra of all possible forms of CXXXOX (X = H, D) molecules demonstrated that the isotopic contamination can be identified due to a coexistence of bands specific to OH and OD groups. Also, bands from partially deuterated methyl groups can be distinguished in NIR spectra. Since the VPT2 framework is known to be sensitive to inaccuracy in the case of highly anharmonic modes, we obtained an independent insight by numerical solving of the time-independent Schrödinger equation corresponding to the O-X stretching mode scanned within -0.4 to 2.0 Å over a dense grid of 0.005 Å. This way the energies of vibrational levels of the CX1X2X3OX4 (X = H, D) isotopomers and the corresponding transition frequencies were obtained with high accuracy (<0.1 cm -1 ). The change in normal coordinate influences the reduced mass of the oscillator and thus its frequency. Our results lead to a conclusion that the effect of deuterization of the methyl group introduces a very specific and consistent frequency shift of the first overtone of the O-X stretching mode depending on the substitution of X1, X2, or X3 positions (<2 cm -1 ). However, the pattern of this shift is not reproduced accurately and is also largely overestimated by VPT2

Fingerprinting groundwater salinity sources in the Gulf Coast Aquifer System, USA

Science.gov (United States)

Chowdhury, Ali H.; Scanlon, Bridget R.; Reedy, Robert C.; Young, Steve

2018-02-01

Understanding groundwater salinity sources in the Gulf Coast Aquifer System (GCAS) is a critical issue due to depletion of fresh groundwater and concerns for potential seawater intrusion. The study objective was to assess sources of groundwater salinity in the GCAS using ˜1,400 chemical analyses and ˜90 isotopic analyses along nine well transects in the Texas Gulf Coast, USA. Salinity increases from northeast (median total dissolved solids (TDS) 340 mg/L) to southwest (median TDS 1,160 mg/L), which inversely correlates with the precipitation distribution pattern (1,370- 600 mm/yr, respectively). Molar Cl/Br ratios (median 540-600), depleted δ2H and δ18O (-24.7‰, -4.5‰) relative to seawater (Cl/Br ˜655 and δ2H, δ18O 0‰, 0‰, respectively), and elevated 36Cl/Cl ratios (˜100), suggest precipitation enriched with marine aerosols as the dominant salinity source. Mass balance estimates suggest that marine aerosols could adequately explain salt loading over the large expanse of the GCAS. Evapotranspiration enrichment to the southwest is supported by elevated chloride concentrations in soil profiles and higher δ18O. Secondary salinity sources include dissolution of salt domes or upwelling brines from geopressured zones along growth faults, mainly near the coast in the northeast. The regional extent and large quantities of brackish water have the potential to support moderate-sized desalination plants in this location. These results have important implications for groundwater management, suggesting a current lack of regional seawater intrusion and a suitable source of relatively low TDS water for desalination.

Do laboratory salinity tolerances of freshwater animals correspond with their field salinity?

Energy Technology Data Exchange (ETDEWEB)

Kefford, Ben J.; Papas, Phil J.; Metzeling, Leon; Nugegoda, Dayanthi

2004-06-01

The degree to which laboratory derived measures of salinity tolerance reflect the field distributions of freshwater biota is uncertain. In this paper we compare laboratory-derived acute salinity tolerance (LC{sub 50} values) of freshwater macroinvertebrates (range 5.5-76 mS/cm) and fish (range 2.7-82 mS/cm) from southeastern Australia with the salinity from which they have been collected in the field. Only 4% of the macroinvertebrates were collected at salinity levels substantially higher than their 72-h LC{sub 50} obtained from directly transferring animals from low salinity water to the water they were tested (direct transfer LC{sub 50}). This LC{sub 50} value was correlated with the maximum salinity at which a species had been collected. For common macroinvertebrates, the maximum field salinity was approximated by the direct transfer 72-h LC{sub 50}. For adult freshwater fish, 21% of species were collected at salinities substantially greater than their acute direct transfer LC{sub 50} and there was a weak relationship between these two variables. Although there was a weak correlation between the direct transfer LC{sub 50} of early life stages of freshwater fish and the maximum field salinity, 58% of the field distribution were in higher than their LC{sub 50} values. In contrast, LC{sub 50} determined from experiments that acclimated adult fish to higher salinity (slow acclimation) provided a better indication of the field distribution: with only one fish species (7%) being in conflict with their maximum field salinity and a strong positive relationship between these variables. This study shows that laboratory measures of acute salinity tolerance can reflect the maximum salinity that macroinvertebrate and fish species inhabit and are consistent with some anecdotal observations from other studies. - Acute laboratory salinity tolerances relate to maximum salinity where organisms occur in nature.

Do laboratory salinity tolerances of freshwater animals correspond with their field salinity?

International Nuclear Information System (INIS)

Kefford, Ben J.; Papas, Phil J.; Metzeling, Leon; Nugegoda, Dayanthi

2004-01-01

The degree to which laboratory derived measures of salinity tolerance reflect the field distributions of freshwater biota is uncertain. In this paper we compare laboratory-derived acute salinity tolerance (LC 50 values) of freshwater macroinvertebrates (range 5.5-76 mS/cm) and fish (range 2.7-82 mS/cm) from southeastern Australia with the salinity from which they have been collected in the field. Only 4% of the macroinvertebrates were collected at salinity levels substantially higher than their 72-h LC 50 obtained from directly transferring animals from low salinity water to the water they were tested (direct transfer LC 50 ). This LC 50 value was correlated with the maximum salinity at which a species had been collected. For common macroinvertebrates, the maximum field salinity was approximated by the direct transfer 72-h LC 50 . For adult freshwater fish, 21% of species were collected at salinities substantially greater than their acute direct transfer LC 50 and there was a weak relationship between these two variables. Although there was a weak correlation between the direct transfer LC 50 of early life stages of freshwater fish and the maximum field salinity, 58% of the field distribution were in higher than their LC 50 values. In contrast, LC 50 determined from experiments that acclimated adult fish to higher salinity (slow acclimation) provided a better indication of the field distribution: with only one fish species (7%) being in conflict with their maximum field salinity and a strong positive relationship between these variables. This study shows that laboratory measures of acute salinity tolerance can reflect the maximum salinity that macroinvertebrate and fish species inhabit and are consistent with some anecdotal observations from other studies. - Acute laboratory salinity tolerances relate to maximum salinity where organisms occur in nature

Evaluation of the Marine Intrusion in Havana Province Groundwater Using Hydrochemical and Isotopic Tools

Energy Technology Data Exchange (ETDEWEB)

Alvarez, A. M.; Bombuse, D. L.; Estevez Alvarez, J. R. [Centro de Aplicaciones Tecnologicas y Desarrollo Nuclear (CEADEN), Havana (Cuba); others, and

2013-07-15

In the present paper the spatial distribution and temporal evolution of the saline intrusion in the most important aquifer of Havana province is presented. Results were obtained through the application of hydrochemical and isotopic tools. Studies were carried out within the framework of the IAEA Regional Project RLA/8/041. The survey was carried out in 2008 during the dry and rainy seasons. Sampling points were selected according to a monitoring network located along the north-south line following the main groundwater flow direction. Stable isotopes ({sup 2}H and {sup 18}O) were used to identify and characterize the groundwater origin and mixing processes. Changes in the chemical composition of groundwater were shown to be mainly controlled by the groundwater and seawater mixing process, followed by cation exchange reactions and a Ca-Mg precipitation process due to the strong influence of the costal wetland. A gradual decreasing of the spatial and temporal saline intrusion was observed. (author)

Stable-isotope paleoclimatology

International Nuclear Information System (INIS)

Deuser, W.G.

1978-01-01

Seasonal variations of temperature and salinity in the surface waters of large parts of the oceans are well established. Available data on seasonal distributions of planktonic foraminifera show that the abundances of different species groups peak at different times of the year with an apparent succession of abundance peaks through most of the year. This evidence suggests that a measure of seasonal contrast is recorded in the isotope ratios of oxygen, and perhaps carbon, in the tests of different foraminiferal species. The evaluation of this potential paleoclimatologic tool awaits planned experiments with recent foraminifera in well-known settings, but a variety of available data is consistent with the idea that interspecies differences in 18 O content contain a seasonal component.(auth.)

A Tiered Approach to Evaluating Salinity Sources in Water at Oil and Gas Production Sites.

Science.gov (United States)

Paquette, Shawn M; Molofsky, Lisa J; Connor, John A; Walker, Kenneth L; Hopkins, Harley; Chakraborty, Ayan

2017-09-01

A suspected increase in the salinity of fresh water resources can trigger a site investigation to identify the source(s) of salinity and the extent of any impacts. These investigations can be complicated by the presence of naturally elevated total dissolved solids or chlorides concentrations, multiple potential sources of salinity, and incomplete data and information on both naturally occurring conditions and the characteristics of potential sources. As a result, data evaluation techniques that are effective at one site may not be effective at another. In order to match the complexity of the evaluation effort to the complexity of the specific site, this paper presents a strategic tiered approach that utilizes established techniques for evaluating and identifying the source(s) of salinity in an efficient step-by-step manner. The tiered approach includes: (1) a simple screening process to evaluate whether an impact has occurred and if the source is readily apparent; (2) basic geochemical characterization of the impacted water resource(s) and potential salinity sources coupled with simple visual and statistical data evaluation methods to determine the source(s); and (3) advanced laboratory analyses (e.g., isotopes) and data evaluation methods to identify the source(s) and the extent of salinity impacts where it was not otherwise conclusive. A case study from the U.S. Gulf Coast is presented to illustrate the application of this tiered approach. © 2017, National Ground Water Association.

Reply to Nicholson's comment on "Consistent calculation of aquatic gross production from oxygen triple isotope measurements" by Kaiser (2011

Directory of Open Access Journals (Sweden)

J. Kaiser

2012-08-01

Full Text Available The comment by Nicholson (2011a questions the "consistency" of the "definition" of the "biological end-member" used by Kaiser (2011a in the calculation of oxygen gross production. "Biological end-member" refers to the relative oxygen isotope ratio difference between photosynthetic oxygen and Air-O₂ (abbreviated ¹⁷δ_P and ¹⁸δ_P for ¹⁷O/¹⁶O and ¹⁸O/¹⁶O, respectively. The comment claims that this leads to an overestimate of the discrepancy between previous studies and that the resulting gross production rates are "30% too high". Nicholson recognises the improved accuracy of Kaiser's direct calculation ("dual-delta" method compared to previous approximate approaches based on ¹⁷O excess (¹⁷Δ and its simplicity compared to previous iterative calculation methods. Although he correctly points out that differences in the normalised gross production rate (g are largely due to different input parameters used in Kaiser's "base case" and previous studies, he does not acknowledge Kaiser's observation that iterative and dual-delta calculation methods give exactly the same g for the same input parameters (disregarding kinetic isotope fractionation during air-sea exchange. The comment is based on misunderstandings with respect to the "base case" ¹⁷δ_P and ¹⁸δ_P values. Since direct measurements of ¹⁷δ_P and ¹⁸δ_Pdo not exist or have been lost, Kaiser constructed the "base case" in a way that was consistent and compatible with literature data. Nicholson showed that an alternative reconstruction of ¹⁷δ_P gives g values closer to previous studies. However, unlike Nicholson, we refrain from interpreting either reconstruction as a benchmark for the accuracy of g. A number of publications over the last 12 months

Salinity-Dependent Adhesion Response Properties of Aluminosilicate (K-Feldspar) Surfaces

DEFF Research Database (Denmark)

Lorenz, Bärbel; Ceccato, Marcel; Andersson, Martin Peter

2017-01-01

is composed predominantly of quartz with some clay, but feldspar grains are often also present. While the wettability of quartz and clay surfaces has been thoroughly investigated, little is known about the adhesion properties of feldspar. We explored the interaction of model oil compounds, molecules...... in well sorted sandstone. Adhesion forces, measured with the chemical force mapping (CFM) mode of atomic force microscopy (AFM), showed a low salinity effect on the fresh feldspar surfaces. Adhesion force, measured with -COO(H)-functionalized tips, was 60% lower in artificial low salinity seawater (LS......, ∼1500 ppm total dissolved solids) than in the high salinity solution, artificial seawater (HS, ASW, ∼35 600 ppm). Adhesion with the -CH3 tips was as much as 30% lower in LS than in HS. Density functional theory calculations indicated that the low salinity response resulted from expansion of the electric...

Isotope geochemistry of fluid inclusions in Permian halite with implications for the isotopic history of ocean water and the origin of saline formation waters

International Nuclear Information System (INIS)

Knauth, L.P.; Beeunas, M.A.

1986-01-01

deltaD and delta 18 O values have been determined for fluid inclusions in 45 samples of Permian halite. The inclusions are enriched in 18 O relative to the meteoric water line but are depleted in D relative to ocean water. Inclusions with the more positive delta-values coincide with the isotopic compositions expected for evaporating sea water which follows a hooked trajectory on a deltaD-delta 18 O diagram. Inclusions with more negative delta-values may represent more highly evaporated sea water but probably reflect synsedimentary or diagenetic mixing to those of a modern evaporite pan to indicate that Permian sea water was isotopically similar to modern sea water. Connate evaporite brines can have negative delta-values because of the probable hooked isotope trajectory of evaporating sea water and/or synsedimentary mixing of evaporite brines with meteoric waters. (author)

Susceptibility to saline contamination of coastal confined aquifer of the Uraba banana axis with hydrogeochemical and isotopic techniques

International Nuclear Information System (INIS)

Paredes Zuniga, Vanessa

2010-01-01

The project has covered an area of study of 8916 km 2 is located in the Northwestern part of the Department of Antioquia, Colombia. Interest area is geologically constituted by tertiary sedimentary rocks (T1 and T2) and alluvial deposits (Quaternary). Hydrogeological units, potentially better use of groundwater, have been established for the unit T2 (confined aquifer) and quaternary deposits.) The area has been of 2600 mm/year to 3600 mm/year of average rainfall. The susceptibility to saline contamination has been determined of coastal aquifer of the Uraba banana axis. Hydrochemical and geological information, geophysics, hydraulic and hydrochemical is used improving existing conceptual hydrogeological model. A hydrochemical characterization has been performed to evaluate the processes of salinity in the confined aquifer. The integration of geological information, geophysical and hydrogeological has been methodology used to validate the hydraulic characteristics of the aquifer, its geometry and operation, updating the conceptual hydrogeological model. The use of complementary tools been able to determine and identify processes that may affect natural physico-chemical characteristics of groundwater. The results have showed that salinization processes present in the coastal aquifer of Uraba Banana Axis could be linked to water-rock interaction, to mixtures with water have become saline as a result of transgression - regression processes in the former study. The hydrogeochemical techniques have become a complementary tool to the hydrogeology allowing respond the questions were presented in complex systems, such as the case of coastal aquifers, where sanitation is usually associated with saline intrusion processes and can also be obeying the conjunction with other hydroclimatological and hydrodynamic aspects. (author) [es

Calculations of the Low-Lying Structures in the Even-Even Nd/Sm/Gd/Dy Isotopes

Science.gov (United States)

Lee, Su Youn; Lee, J. H.; Lee, Young Jun

2018-05-01

The nuclear structure of deformed nuclei has been studied using the interacting boson model (IBM). In this study, energy levels and E2 transition probabilities were determined for even nuclei in the Nd/Sm/Gd/Dy chains which have a transition characteristic between the rotational, SU(3) and vibrational, U(5) limits. The structure of the nuclei exhibits a slight breaking of the SU(3) symmetry in the direction of U(5), and therefore, we add the d-boson number operator n d , which is the main term of the U(5) symmetric Hamiltonian, to the SU(3) Hamiltonian of the IBM. The calculated results for low-lying energy levels and E2 transition rates in Nd/Sm/Gd/Dy isotopes are in reasonably good agreement with known experimental results.

Salinity Effects on Germination Properties ofPurslane (Portulaca oleracea L.

Directory of Open Access Journals (Sweden)

m Kafi

2011-02-01

Full Text Available Abstract In order to study seed germination and seedling growth responses of purslane to different levels of salinity, an experiment was conducted in a completely randomized desgin with six levels of salinity (0, 7, 14, 21, 28 and 35 dS/m using NaCl and five replications. Persentage and rate of germination, length and dry weight of radicle and plumule were measured, and ratio radicle to plumule length, mean germination time and seedling vigor index were calculated. The results showed that up to 28 dS/m salinity did not impose any significant different in germination percentage compared with control, but in 35 dS/m salinity it decreased to 19%. germination rate did not show any significant different up to 14 dS/m in comparison with control but beyond this level it significantly decreased with increasing salt stress. Mean germination time up to 21 dS/m did not have significant different in comparison with control, but increased with increasing salinity significantly. Length, fresh and dry weight of radicle and plumule, and seedling vigor index significantly decreased by increasing salinity. Ratio of radicle to plumule length decreased with increasing salt concentration, but there were not significant different among salt levels. According to the results, the germination stage of purslane is remarkably resistant to elevated levels of salinity and it seems that by exerting proper management in farms, it could be established in saline environments. Keywords: Plumule, Radicle, Seedlings of purslane

Calculation of electron and isotopes dose point kernels with FLUKA Monte Carlo code for dosimetry in nuclear medicine therapy

CERN Document Server

Mairani, A; Valente, M; Battistoni, G; Botta, F; Pedroli, G; Ferrari, A; Cremonesi, M; Di Dia, A; Ferrari, M; Fasso, A

2011-01-01

Purpose: The calculation of patient-specific dose distribution can be achieved by Monte Carlo simulations or by analytical methods. In this study, FLUKA Monte Carlo code has been considered for use in nuclear medicine dosimetry. Up to now, FLUKA has mainly been dedicated to other fields, namely high energy physics, radiation protection, and hadrontherapy. When first employing a Monte Carlo code for nuclear medicine dosimetry, its results concerning electron transport at energies typical of nuclear medicine applications need to be verified. This is commonly achieved by means of calculation of a representative parameter and comparison with reference data. Dose point kernel (DPK), quantifying the energy deposition all around a point isotropic source, is often the one. Methods: FLUKA DPKS have been calculated in both water and compact bone for monoenergetic electrons (10-3 MeV) and for beta emitting isotopes commonly used for therapy ((89)Sr, (90)Y, (131)I, (153)Sm, (177)Lu, (186)Re, and (188)Re). Point isotropic...

Selective heating and separation of isotopes in a metallic plasma

International Nuclear Information System (INIS)

Moffa, P.; Cheshire, D.; Flanders, B.; Myer, R.; Robinette, W.; Thompson, J.; Young, S.

1983-01-01

Several types of metallic plasmas have been produced at the Plasma Separation Process facility of TRW. Selective heating and separation of specific isotopes in these plasmas have been achieved. In this presentation the authors concentrate on the modeling of the selective heating and separation of the isotope Ni 58 . Two models are currently used to describe the excitation process. In both, the electromagnetic fields in the plasma produced by the ICRH antenna are calculated self-consistently using a kinetic description of the warm plasma dielectric. In the Process Model Code, both the production of the plasma and the heating are calculated using a Monte Carlo approach. Only the excitation process is treated in the second simplified model. Test particles that sample an initial parallel velocity distribution are launched into the heating region and the equations of motion including collisional damping are calculated. For both models, the perpendicular energy for a number of particles with different initial conditions and representing the different isotopes is calculated. This information is then input into a code that models the performance of our isotope separation collector. The motion of the ions of each isotope through the electrically biased collector is followed. An accounting of where each particle is deposited is kept and hence the isotope separation performance of the collector is predicted

Calculation of carbon-14, chlorine-37, and deuterium kinetic isotope effects in the solvolysis of tert-butyl chloride

International Nuclear Information System (INIS)

Burton, G.W.; Sims, L.B.; Wilson, J.C.; Fry, A.

1977-01-01

In the solvolysis of tert-butyl chloride, satisfactory α-carbon-14, β-deuterium, and chlorine kinetic isotope effects (KIE) may be calculated for a productlike transition state characterized by bond orders n/sub C Cl/ = 0.2, n/sub C C/ = 1.18, and n/sub C H/ = 0.94, employing a diagonal valence force field, provided that allowance is made for hydrogen-bonded solvation of the developing chloride ion with n/sub Cl H/ approx. 0.05 (approx. 7 kcal/mole hydrogen bonds). The effect of the three solvating molecules appears to be to increase the ''effective'' mass of the incipient chloride ion and to decrease the loss of zero-point energy in going to the transition state. Reaction coordinates more complicated than a simple heterolysis of the carbon-chlorine bond appear to be unnecessary and there is no advantage in employing force fields more complex than a simple valence force field containing only diagonal elements for both the reactant and the transition state model. The structural and bonding features of the proposed transition state are in accord with earlier more qualitative conclusions concerning the polar nature and productlike character of the transition state, and provide a reasonable explanation of the kinetic and equilibrium isotope effects (EIE) for the reaction. An alternative transition state model involving weak solvent nucleophilic assistance provides reasonable calculated values for the KIE, but the EIE strongly suggest the importance of solvation of the leaving group which, together with the hyperconjugation of the β hydrogens, provides a preferred explanation of the tert-butyl solvolysis results

Water isotopic characterization of hypersaline formation of a petroleum field Reconcavo basin, Brazil

International Nuclear Information System (INIS)

Teles, Danilo Ribeiro de Sa; Azevedo, Antonio Expedito Gomes de

2010-01-01

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 (δ 2 H , δ 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 δ 2 H , δ 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)

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

International Nuclear Information System (INIS)

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

1993-01-01

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

New approximations for the interference term applied to the calculation of scattering cross section of the 238 U isotope

International Nuclear Information System (INIS)

Palma, Daniel Artur Pinheiro; Martinez, Aquilino Senra; Goncalves, Alessandro C.

2008-01-01

The calculation of the Doppler broadening function and the interference term are very important in the generation of nuclear data. Recent papers have proposed analytical formulations for both functions and, despite their being simple and precise, they contain the error function with a complex argument. With the intention of simplifying the mathematical treatment two approximations are proposed in this paper. The first one consists of using an expansion in the form of series to treat the error function. The other approximation is based on simplifications in the differential equations that govern the Doppler broadening function. For validation purpose the result obtained is compared to the one obtained in the calculation of the cross sections for isotope 238 U for different resonances. Results obtained have proved satisfactory from the standpoint of accuracy. (author)

The isotopic dipole moment of HDO

Energy Technology Data Exchange (ETDEWEB)

Assafrao, Denise; Mohallem, Jose R [Laboratorio de Atomos e Moleculas Especiais, Departamento de Fisica, ICEx, Universidade Federal de Minas Gerais, CP 702, 30123-970, Belo Horizonte, MG (Brazil)

2007-03-14

An adiabatic variational approximation is used to study the monodeuterated water molecule, HDO, accounting for the isotopic effect. The isotopic dipole moment, pointing from D to H, is then calculated for the first time, yielding (1.5 {+-} 0.1) x 10{sup -3} Debye, being helpful in the interpretation of experiments. (fast track communication)

Absolute Salinity, ''Density Salinity'' and the Reference-Composition Salinity Scale: present and future use in the seawater standard TEOS-10

Science.gov (United States)

Wright, D. G.; Pawlowicz, R.; McDougall, T. J.; Feistel, R.; Marion, G. M.

2011-01-01

Salinity plays a key role in the determination of the thermodynamic properties of seawater and the new TEOS-101 standard provides a consistent and effective approach to dealing with relationships between salinity and these thermodynamic properties. However, there are a number of practical issues that arise in the application of TEOS-10, both in terms of accuracy and scope, including its use in the reduction of field data and in numerical models. First, in the TEOS-10 formulation for IAPSO Standard Seawater, the Gibbs function takes the Reference Salinity as its salinity argument, denoted SR, which provides a measure of the mass fraction of dissolved material in solution based on the Reference Composition approximation for Standard Seawater. We discuss uncertainties in both the Reference Composition and the Reference-Composition Salinity Scale on which Reference Salinity is reported. The Reference Composition provides a much-needed fixed benchmark but modified reference states will inevitably be required to improve the representation of Standard Seawater for some studies. However, the Reference-Composition Salinity Scale should remain unaltered to provide a stable representation of salinity for use with the TEOS-10 Gibbs function and in climate change detection studies. Second, when composition anomalies are present in seawater, no single salinity variable can fully represent the influence of dissolved material on the thermodynamic properties of seawater. We consider three distinct representations of salinity that have been used in previous studies and discuss the connections and distinctions between them. One of these variables provides the most accurate representation of density possible as well as improvements over Reference Salinity for the determination of other thermodynamic properties. It is referred to as "Density Salinity" and is represented by the symbol SAdens; it stands out as the most appropriate representation of salinity for use in dynamical physical

Absolute Salinity, "Density Salinity" and the Reference-Composition Salinity Scale: present and future use in the seawater standard TEOS-10

Science.gov (United States)

Wright, D. G.; Pawlowicz, R.; McDougall, T. J.; Feistel, R.; Marion, G. M.

2010-08-01

Salinity plays a key role in the determination of the thermodynamic properties of seawater and the new TEOS-101 standard provides a consistent and effective approach to dealing with relationships between salinity and these thermodynamic properties. However, there are a number of practical issues that arise in the application of TEOS-10, both in terms of accuracy and scope, including its use in the reduction of field data and in numerical models. First, in the TEOS-10 formulation for IAPSO Standard Seawater, the Gibbs function takes the Reference Salinity as its salinity argument, denoted SR, which provides a measure of the mass fraction of dissolved material in solution based on the Reference Composition approximation for Standard Seawater. We discuss uncertainties in both the Reference Composition and the Reference-Composition Salinity Scale on which Reference Salinity is reported. The Reference Composition provides a much-needed fixed benchmark but modified reference states will inevitably be required to improve the representation of Standard Seawater for some studies. The Reference-Composition Salinity Scale should remain unaltered to provide a stable representation of salinity for use with the TEOS-10 Gibbs function and in climate change detection studies. Second, when composition anomalies are present in seawater, no single salinity variable can fully represent the influence of dissolved material on the thermodynamic properties of seawater. We consider three distinct representations of salinity that have been used in previous studies and discuss the connections and distinctions between them. One of these variables provides the most accurate representation of density possible as well as improvements over Reference Salinity for the determination of other thermodynamic properties. It is referred to as "Density Salinity" and is represented by the symbol SAdens; it stands out as the most appropriate representation of salinity for use in dynamical physical

Diatom-induced silicon isotopic fractionation in Antarctic sea ice

Science.gov (United States)

Francois, F.; Damien, C.; Jean-Louis, T.; Anthony, W.; Luc, A.

2006-12-01

We measured silicon-isotopic composition of dissolved silicon and biogenic silica collected by sequential melting from spring 2003 Antarctic pack ice (Australian sector). Sea ice is a key ecosystem in the Southern Ocean and its melting in spring has been often thought to have a seeding effect for the surface waters, triggering blooms in the mixed layer. This work is the first investigation of the silicon isotopes' proxy in sea ice and allows to estimate the activity of sea-ice diatoms in the different brine structures and the influence of sea- ice diatoms on the spring ice edge blooms. The relative use of the dissolved silicon pool by sea-ice diatoms is usually assessed by calculating nutrient:salinity ratios in the brines. However such an approach is biased by difficulties in evaluating the initial nutrient concentrations in the different brines structures, and by the impossibility to account for late sporadic nutrient replenishments. The silicon-isotopic composition of biogenic silica is a convenient alternative since it integrates an average Si utilization on all generations of diatoms. Measurements were performed on a MC-ICP-MS, in dry plasma mode using external Mg doping. Results are expressed as delta29Si relative to the NBS28 standard. From three sea ice cores with contrasted physico-chemical characteristics, we report significant isotopic fractionations linked to the diatoms activity, with distinct silicon biogeochemical dynamics between different brine structure. The diatoms in snow ice and in brine pockets of frazil or congelation ice have the most positive silicon-isotopic composition (+0.53 to +0.86 p.mil), indicating that they grow in a closed system and use a significant part of the small dissolved silicon pool. In the brine channels and skeletal layer, diatoms display a relatively less positive Si-isotopic composition (+0.41 to +0.70 p.mil), although it is still heavier compared to equilibrium fractionation (+0.38 p.mil). This suggests that they have

Calculation of the absorbed dose for contamination in skin imparted by beta radiation through the Varskin code modified for 122 isotopes of interest for nuclear medicine, nuclear plants and research

International Nuclear Information System (INIS)

Alvarez R, J.T.

1992-06-01

In this work the implementation of a modification of the Varskin code for calculation of absorbed dose by contamination in skin imparted by external radiation fields generated by beta emitting is presented. The necessary data for the execution of the code are: isotope, dose depth, isotope activity, geometry type, source radio and time of integration of the isotope, being able to execute combinations of up to five radionuclides. This program it was implemented in Fortran 5 by means of the FFSKIN source program and the executable one in binary language BFFSKIN being the maximum execution time of 5 minutes. (Author)

Exploring the isotopic niche: isotopic variance, physiological incorporation, and the temporal dynamics of foraging

Directory of Open Access Journals (Sweden)

Justin Douglas Yeakel

2016-01-01

Full Text Available Consumer foraging behaviors are dynamic, changing in response to prey availability, seasonality, competition, and even the consumer's physiological state. The isotopic composition of a consumer is a product of these factors as well as the isotopic `landscape' of its prey, i.e. the isotopic mixing space. Stable isotope mixing models are used to back-calculate the most likely proportional contribution of a set of prey to a consumer's diet based on their respective isotopic distributions, however they are disconnected from ecological process. Here we build a mechanistic framework that links the ecological and physiological processes of an individual consumer to the isotopic distribution that describes its diet, and ultimately to the isotopic composition of its own tissues, defined as its `isotopic niche’. By coupling these processes, we systematically investigate under what conditions the isotopic niche of a consumer changes as a function of both the geometric properties of its mixing space and foraging strategies that may be static or dynamic over time. Results of our derivations reveal general insight into the conditions impacting isotopic niche width as a function of consumer specialization on prey, as well as the consumer's ability to transition between diets over time. We show analytically that moderate specialization on isotopically unique prey can serve to maximize a consumer's isotopic niche width, while temporally dynamic diets will tend to result in peak isotopic variance during dietary transitions. We demonstrate the relevance of our theoretical findings by examining a marine system composed of nine invertebrate species commonly consumed by sea otters. In general, our analytical framework highlights the complex interplay of mixing space geometry and consumer dietary behavior in driving expansion and contraction of the isotopic niche. Because this approach is established on ecological mechanism, it is well-suited for enhancing the

Using cosmogenic isotopes to measure basin-scale rates of erosion

International Nuclear Information System (INIS)

Bierman, P.R.; Steig, E.

1992-01-01

The authors present a new and different approach to interpreting the abundance of in situ-produced cosmogenic nuclides such as 36 Cl, 26 Al, and 10 Be. Unlike most existing models, which are appropriate for evaluating isotope concentrations on bedrock surfaces, this model can be used to interpret isotope concentration in fluvial sediment. Because sediment is a mixture of material derived from the entire drainage basin, measured isotope abundances can be used to estimate spatially-averaged rates of erosion and sediment transport. Their approach has the potential to provide geomorphologists with a relatively simple but powerful means by which to constrain rates of landscape evolution. The model considers the flux of cosmogenic isotopes into and out of various reservoirs. Implicit in model development are the assumptions that a geomorphic steady-state has been reached and that sampled sediment is spatially and temporally representative of all sediment leaving the basin. Each year, the impinging cosmic-ray flux produces a certain quantity of cosmogenic isotopes in the rock and soil of a drainage basin. For a basin in steady state, the outgoing isotope flux is also constant. They solve for the rate of mass loss as a function of isotope abundance in the sediment, the cosmic ray attenuation length, the isotope half life, and the effective isotope production rate. There are only a few published measurements of cosmogenic isotope abundance in sediment. They calculated model denudation rates for sediment samples from Zaire and central Texas. The denudation rates they calculated appear reasonable and are similar to those they have measured directly on granite landforms in Georgia and southeastern California and those calculated for the Appalachian Piedmont

The effect of vesicular-arbuscular mycorrhiza isolated from Syrian soil on alfalfa growth and nitrogen fixation in saline soil

International Nuclear Information System (INIS)

El Atrash, F

2001-01-01

The influence of vesicular - arbuscular Mycorrhiza fungi (VAM) on symbiotic fixation of N 2 n alfalfa plants has been observed. Beneficial effects of study the effect of VAM or phosphorous fertilization on alfalfa (Medicago sativa L,) yields, umber of nodules and N 2 fixation by N 15 isotope dilution at different salinity levels. This experiment was realized in green house conditions, using soil of 2.3 dsm -1 conductivity mixed with sand (5: 2V) for alfalfa plants growing at various levels of phosphorus, or infected by Mycorrhiza fungi. Different conductivities (13.18, 22.2, 28.8, 43.5 dsm -1 ) were applied on these treatment by increasing concentrations of Nacl, CaCl 2 and MgCl 2 and MgCl 2 by salinity soil irrigation. Ten days after planting, soil was enriched with 2 ppm of (NH 4 15 ) 2 SO 4 . Plant were grown under greenhouse condition for ten weeks. Our results confirmed that increased salinity reduced nitrogen - fixation and the number of nodules. The negative effect with increasing salinity was less in Mycorrhiza plants than in plants fertilized with various levels of phosphorus, and only the higher levels of salinity reduced significantly, the percentage of Mycorrhiza colonization, However, at all levels of salinity, VAM stimulated plant growth and nutrient uptake. (author)

The common property of isotope anomalies in meteorites

International Nuclear Information System (INIS)

Robert, F.

2004-01-01

The treatment proposed to account for the non-mass-dependent isotopic fractionation effect observed for oxygen isotopes during the synthesis of ozone (Robert and Camy-Peyret 2001) is applied to other chemical elements. A numerical treatment to calculate isotopic reaction rate ratios is proposed. This treatment yields non-mass-dependent isotopic effects in other chemical elements, qualitatively similar to those observed in some of the high temperature minerals found in the carbonaceous meteorites. This treatment may reflect the numerical consequences of an unrecognized quantum mechanical effect, linked to a property of chemical reactions involving indistinguishable isotopes. (author)

Surface Energy Balance of Fresh and Saline Waters: AquaSEBS

Directory of Open Access Journals (Sweden)

Ahmed Abdelrady

2016-07-01

Full Text Available Current earth observation models do not take into account the influence of water salinity on the evaporation rate, even though the salinity influences the evaporation rate by affecting the density and latent heat of vaporization. In this paper, we adapt the SEBS (Surface Energy Balance System model for large water bodies and add the effect of water salinity to the evaporation rate. Firstly, SEBS is modified for fresh-water whereby new parameterizations of the water heat flux and sensible heat flux are suggested. This is achieved by adapting the roughness heights for momentum and heat transfer. Secondly, a salinity correction factor is integrated into the adapted model. Eddy covariance measurements over Lake IJsselmeer (The Netherlands are carried out and used to estimate the roughness heights for momentum (~0.0002 m and heat transfer (~0.0001 m. Application of these values over the Victoria and Tana lakes (freshwater in Africa showed that the calculated latent heat fluxes agree well with the measurements. The root mean-square of relative-errors (rRMSE is about 4.1% for Lake Victoria and 4.7%, for Lake Tana. Verification with ECMWF data showed that the salinity reduced the evaporation at varying levels by up to 27% in the Great Salt Lake and by 1% for open ocean. Our results show the importance of salinity to the evaporation rate and the suitability of the adapted-SEBS model (AquaSEBS for fresh and saline waters.

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

International Nuclear Information System (INIS)

Zimmerman, M.G.

1977-06-01

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

A groundwater salinity hotspot and its connection to an intermittent stream identified by environmental tracers (Mt Lofty Ranges, South Australia)

Science.gov (United States)

Anderson, Thomas A.; Bestland, Erick A.; Soloninka, Lesja; Wallis, Ilka; Banks, Edward W.; Pichler, Markus

2017-12-01

High and variable levels of salinity were investigated in an intermittent stream in a high-rainfall area (˜800 mm/year) of the Mt. Lofty Ranges of South Australia. The groundwater system was found to have a local, upslope saline lens, referred to here as a groundwater salinity `hotspot'. Environmental tracer analyses (δ18O, δ2H, 87/86Sr, and major elements) of water from the intermittent stream, a nearby permanent stream, shallow and deep groundwater, and soil-water/runoff demonstrate seasonal groundwater input of very saline composition into the intermittent stream. This input results in large salinity increases of the stream water because the winter wet-season stream flow decreases during spring in this Mediterranean climate. Furthermore, strontium and water isotope analyses demonstrate: (1) the upslope-saline-groundwater zone (hotspot) mixes with the dominant groundwater system, (2) the intermittent-stream water is a mixture of soil-water/runoff and the upslope saline groundwater, and (3) the upslope-saline-groundwater zone results from the flushing of unsaturated-zone salts from the thick clayey regolith and soil which overlie the metamorphosed shale bedrock. The preferred theory on the origin of the upslope-saline-groundwater hotspot is land clearing of native deep-rooted woodland, followed by flushing of accumulated salts from the unsaturated zone due to increased recharge. This cause of elevated groundwater and surface-water salinity, if correct, could be widespread in Mt. Lofty Ranges areas, as well as other climatically and geologically similar areas with comparable hydrogeologic conditions.

The use of environmental isotopes on groundwater hydrology in the selected areas in Thailand

International Nuclear Information System (INIS)

Buapeng, S.

1990-11-01

A detailed environmental isotope investigation (using 0-18, H-2, H-3, C-14 and C-13 isotopes) has been carried out in a multi-layer aquifer system of the Chao-Phraya basin in Thailand. The main emphasis of the applied field research has been placed on the delineation of genesis of water and on studying the regional replenishment and flow characteristics of the groundwater in the lower Chao-Phraya basin (Bangkok Metropolitan Area). The results of isotope data gathered have been evaluated along with hydrochemical and basic hydrogeological data, to provide quantitative information on the replenishment characteristics of the groundwater and on the cause and processes involved in the increase of salinity being observed in the groundwater system of the Bangkok area. The report provides all the isotopic results and other relevant data together with interpretation and evaluation of the results. Refs, figs and tabs

Measurement of flowing water salinity within or behind wellbore casing

International Nuclear Information System (INIS)

Arnold, D.M.

1981-01-01

Water flowing within or behind a wellbore casing is irradiated with 14 MeV neutrons from a source in a downhole sonde. Gamma radiation from the isotope nitrogen-16 induced from the O 16 (n,p)N 16 reaction and the products of either the Na 23 (n,α)F 20 or the Cl 37 (n,α)P 34 reactions is measured in intensity and energy with detectors in the sonde. From the gamma radiation measurements, the relative presence of oxygen to at least one of sodium or chlorine in the water is measured, and from the measurement the salinity of the water is to be determined. (author)

Geographical variations in Sr and Nd isotopic ratios of cryoconite on Asian glaciers

International Nuclear Information System (INIS)

Nagatsuka, Naoko; Takeuchi, Nozomu; Nakano, Takanori; Shin, Kicheol; Kokado, Emi

2014-01-01

Cryoconite is a dark-coloured surface dust deposited on glaciers that consists of wind-blown mineral particles, as well as organic matter derived from microbes living on glaciers. In this paper, we analyse the Sr and Nd isotopic ratios of four mineral fractions (i.e., the saline, carbonate, phosphate, and silicate mineral fractions), as well as the organic fraction, of cryoconite samples obtained from six Asian glaciers (the Altai, Pamir, Tien Shan, Qillian Shan, and Himalayan regions), and discuss their geographical variations in terms of the geological origins of the mineral particles and the biogeochemical processes on the glaciers. The silicate mineral fraction showed lower Sr and higher Nd ratios for the glaciers located to the north (Altai, 87 Sr/ 86 Sr: 0.713 490–0.715 284, εNd(0): −6.4 to −5.6), while higher Sr and lower Nd ratios for the glaciers located to the south (Himalayas, 87 Sr/ 86 Sr: 0.740 121–0.742 088, εNd(0): −16.4 to −15.7); the ratios were similar to those of desert sand, loess, and river sediments in the respective regions of the glaciers. This result suggests that the silicate minerals within the cryoconites were derived from different sources depending on the geographical locations of the glaciers. The isotopic ratios of the saline, carbonate, and phosphate mineral fractions were distinct from those of the silicate fraction, and were similar to those of evaporites and apatite deposits from the Asian deserts, but also varied geographically, indicating that they are likely to reflect their geological origin. The Sr isotopic ratios of the organic fraction were similar to those of the saline and carbonate fractions from glaciers in the central area (Tien Shan and Qillian Shan), but were higher than those of the saline and carbonate fractions, and lower than the phosphate mineral fraction, in the northern and southern areas. The ratios of organic fraction may be determined from the mixing ratio of calcium sources

Isotope separation by ionic cyclotron resonance

International Nuclear Information System (INIS)

Compant La Fontaine, A.; Gil, C.; Louvet, P.

1986-10-01

The principle of the process of isotopic separation by ionic cyclotron resonance is explained succinctly. The theoretical calculation of the isotopic effect is given as functions of the electric and magnetic fields in the frame of single particle approximation and of plasma collective theory. Then, the main parts of the demonstration device which is in operation at the CEA, are described here: the supraconducting magnetic field, the used diagnostics, the principle of the source and the collecting apparatus. Some experimental results are given for chromium. The application of the process to ponderal separation of metal isotopes, as chromium, nickel and molybdenum is discussed in view of production of medical, structural and irradiation isotopes

Past 20,000-year history of Himalayan aridity: Evidence from oxygen isotope records in the Bay of Bengal

Digital Repository Service at National Institute of Oceanography (India)

Chauhan, O.S.

Late Quaternary climate history of the Himalayas is inferred from sea surface salinity (SSS) changes determined from the oxygen isotope in planktonic foraminifers, in a turbidity-free, 14C-dated core from the Bay of Bengal. The heaviest d18O...

Remote sensing of drought and salinity stressed turfgrass

Science.gov (United States)

Ikemura, Yoshiaki

The ability to detect early signs of stress in turfgrass stands using a rapid, inexpensive, and nondestructive method would be a valuable management tool. Studies were conducted to determine if digital image analysis and spectroradiometric readings obtained from drought- and salinity-stressed turfgrasses accurately reflected the varying degrees of stress and correlated strongly with visual ratings, relative water content (RWC) and leaf osmolality, standard methods for measuring stress in plants. Greenhouse drought and salinity experiments were conducted on hybrid bluegrass [Poa arachnifera (Torn.) x pratensis (L.)] cv. Reveille and bermudagrass [Cynodon dactylon (L.)] cv. Princess 77. Increasing drought and salinity stress led to decreased RWC, increased leaf osmolality, and decreased visual ratings for both species. Percent green cover and hue values obtained from digital image analysis, and Normalized Difference Vegetation Index (NDVI), calculated from spectroradiometric readings, were moderately to highly correlated with visual ratings, RWC, and leaf osmolality. Similarly, in a field validation study conducted on hybrid bluegrass, spectral reflectance ratios were moderately to highly correlated with visual ratings. In addition, percent green cover obtained from digital image analysis was strongly correlated with most of the spectral ratios, particularly the ratio of fluorescence peaks (r = -0.88 to -0.99), modified triangular vegetation index (MTVI) (r = 0.82 to 0.98), and NDVI (r = 0.84 to 0.99), suggesting that spectral reflectance and digital image analysis are equally effective at detecting changes in color brought on by stress. The two methods differed in their ability to distinguish between drought salinity stress. Hue values obtained from digital image analysis responded differently to increasing drought stress than to increasing salinity stress. Whereas the onset of drought stress was reflected by increased hue values followed by a decrease in values as

Properties of Fe, Ni and Zn isotopes near the drip-lines

International Nuclear Information System (INIS)

Tarasov, V.N.; Tarasaov, D.V.; Gridnev, K.A.; Gridnev, D.K.; Kartavenko, V.G.; Greiner, W.

2008-01-01

The position of the neutron and proton drip-lines as well as properties of the isotopes Fe, Ni and Zn with neutron excess and neutron deficit are studied within the Hartree–Fock approach with the Skyrme interaction (Ska, SkM*, Sly4). The pairing is taken into account on the basis of the BCS approach with the pairing constant G = (19.5/A)[1 ± 0.51(N-Z)/A]. Our calculations predict that for Ni isotopes around N = 62 there appears a sudden increase of the deformation parameter up to β = 0.4. The zone with such big deformation, where Ni isotopes are stable against one neutron emission stretches up to N = 78. The magic numbers effects for the isotopes 48 Ni, 56 Ni, 78 Ni, 110 Ni are discussed. The universality of the reasons standing behind the enhancement of stability of the isotopes 40 O and 110 Ni which are beyond the drip-line is demonstrated. Calculated values of the two-neutron separation energy, and proton and neutron root mean square radii for the chain of Ni isotopes show a good agreement with existing Hartree–Fock–Bogoliubov calculations of these values. (author)

Absolute Salinity, ''Density Salinity'' and the Reference-Composition Salinity Scale: present and future use in the seawater standard TEOS-10

Directory of Open Access Journals (Sweden)

D. G. Wright

2011-01-01

Full Text Available Salinity plays a key role in the determination of the thermodynamic properties of seawater and the new TEOS-10¹ standard provides a consistent and effective approach to dealing with relationships between salinity and these thermodynamic properties. However, there are a number of practical issues that arise in the application of TEOS-10, both in terms of accuracy and scope, including its use in the reduction of field data and in numerical models.

First, in the TEOS-10 formulation for IAPSO Standard Seawater, the Gibbs function takes the Reference Salinity as its salinity argument, denoted S_R, which provides a measure of the mass fraction of dissolved material in solution based on the Reference Composition approximation for Standard Seawater. We discuss uncertainties in both the Reference Composition and the Reference-Composition Salinity Scale on which Reference Salinity is reported. The Reference Composition provides a much-needed fixed benchmark but modified reference states will inevitably be required to improve the representation of Standard Seawater for some studies. However, the Reference-Composition Salinity Scale should remain unaltered to provide a stable representation of salinity for use with the TEOS-10 Gibbs function and in climate change detection studies.

Second, when composition anomalies are present in seawater, no single salinity variable can fully represent the influence of dissolved material on the thermodynamic properties of seawater. We consider three distinct representations of salinity that have been used in previous studies and discuss the connections and distinctions between them. One of these variables provides the most accurate representation of density possible as well as improvements over Reference Salinity for the determination of other thermodynamic properties. It is referred to as "Density Salinity" and is represented by the symbol

Isotope effect on the zero point energy shift upon condensation

International Nuclear Information System (INIS)

Kornblum, Z.C.

1977-01-01

The various isotope-dependent and independent atomic and molecular properties that pertain to the isotopic difference between the zero point energy (ZPE) shifts upon condensation have been derived. The theoretical development of the change of the ZPE associated with the internal molecular vibrations, due to the condensation of the gaseous molecules, has been presented on the basis of Wolfsberg's second-order perturbation treatment of the isotope-dependent London dispersion forces between liquid molecules. The isotope effect on the ZPE shift is related to the difference between the sums of the integrated intensities of the infrared absorption bands of the two gaseous isotopic molecules. Each intensity sum is expressed, in part, in terms of partial derivatives of the molecular dipole moment with respect to atomic cartesian coordinates. These derivatives are related to the isotope-independent effective charges of the atoms, which are theoretically calculated by means of a modified CNDO/2 computer program. The effective atomic charges are also calculated from available experimental infrared intensity data. The effects of isotopic substitutions of carbon-13 for carbon-12 and/or deuterium for protium, in ethylene, methane, and the fluorinated methanes, CH 3 F, CH 2 F 2 , CHF 3 , and CF 4 , on the ZPE shift upon condensation are calculated. These results compare well with the Bigeleisen B-factors, which are experimentally obtained from vapor pressure measurements of the isotopic species. Each of the following molecular properties will tend to increase the isotopic difference between the ZPE shifts upon condensation: (1) large number of highly polar bonds, (2) high molecular weight, (3) non-polar (preferably) or massive molecule, (4) non-hydrogenous molecule, and (5) closely packed liquid molecules. These properties will result in stronger dispersion forces in the liquid phase between the lighter molecules than between the isotopically heavier molecules

Positive parity states and some electromagnetic transition properties of even-odd europium isotopes

Energy Technology Data Exchange (ETDEWEB)

Yazar, Harun Resit, E-mail: yazar@nevsehir.edu.tr [Nevsehir University, Faculty of Art and Science (Turkey)

2013-06-15

The positive-parity low-spin states of even-odd Europium isotopes ({sup 151-155}Eu) were studied within the framework of the interacting boson-fermion model. The calculated positive low-spin state energy spectra of the odd Eu isotope were found to agree quite well with the experimental data. The B(E2) values were also calculated and it was found that the calculated positive-parity low-spin state energy spectra of the odd-A Eu isotopes agree quite well with the experimental data.

Computational Replication of the Primary Isotope Dependence of Secondary Kinetic Isotope Effects in Solution Hydride-Transfer Reactions: Supporting the Isotopically Different Tunneling Ready State Conformations.

Science.gov (United States)

Derakhshani-Molayousefi, Mortaza; Kashefolgheta, Sadra; Eilers, James E; Lu, Yun

2016-06-30

We recently reported a study of the steric effect on the 1° isotope dependence of 2° KIEs for several hydride-transfer reactions in solution (J. Am. Chem. Soc. 2015, 137, 6653). The unusual 2° KIEs decrease as the 1° isotope changes from H to D, and more in the sterically hindered systems. These were explained in terms of a more crowded tunneling ready state (TRS) conformation in D-tunneling, which has a shorter donor-acceptor distance (DAD) than in H-tunneling. To examine the isotopic DAD difference explanation, in this paper, following an activated motion-assisted H-tunneling model that requires a shorter DAD in a heavier isotope transfer process, we computed the 2° KIEs at various H/D positions at different DADs (2.9 Å to 3.5 Å) for the hydride-transfer reactions from 2-propanol to the xanthylium and thioxanthylium ions (Xn(+) and TXn(+)) and their 9-phenyl substituted derivatives (Ph(T)Xn(+)). The calculated 2° KIEs match the experiments and the calculated DAD effect on the 2° KIEs fits the observed 1° isotope effect on the 2° KIEs. These support the motion-assisted H-tunneling model and the isotopically different TRS conformations. Furthermore, it was found that the TRS of the sterically hindered Ph(T)Xn(+) system does not possess a longer DAD than that of the (T)Xn(+) system. This predicts a no larger 1° KIE in the former system than in the latter. The observed 1° KIE order is, however, contrary to the prediction. This implicates the stronger DAD-compression vibrations coupled to the bulky Ph(T)Xn(+) reaction coordinate.

Ethanol-metabolizing pathways in deermice. Estimation of flux calculated from isotope effects

International Nuclear Information System (INIS)

Alderman, J.; Takagi, T.; Lieber, C.S.

1987-01-01

The apparent deuterium isotope effects on Vmax/Km (D(V/K] of ethanol oxidation in two deermouse strains (one having and one lacking hepatic alcohol dehydrogenase (ADH] were used to calculate flux through the ADH, microsomal ethanol-oxidizing system (MEOS), and catalase pathways. In vitro, D(V/K) values were 3.22 for ADH, 1.13 for MEOS, and 1.83 for catalase under physiological conditions of pH, temperature, and ionic strength. In vivo, in deermice lacking ADH (ADH-), D(V/K) was 1.20 +/- 0.09 (mean +/- S.E.) at 7.0 +/- 0.5 mM blood ethanol and 1.08 +/- 0.10 at 57.8 +/- 10.2 mM blood ethanol, consistent with ethanol oxidation principally by MEOS. Pretreatment of ADH- animals with the catalase inhibitor 3-amino-1,2,4-triazole did not significantly change D(V/K). ADH+ deermice exhibited D(V/K) values of 1.87 +/- 0.06 (untreated), 1.71 +/- 0.13 (pretreated with 3-amino-1,2,4-triazole), and 1.24 +/- 0.13 (after the ADH inhibitor, 4-methylpyrazole) at 5-7 mM blood ethanol levels. At elevated blood ethanol concentrations (58.1 +/- 2.4 mM), a D(V/K) of 1.37 +/- 0.21 was measured in the ADH+ strain. For measured D(V/K) values to accurately reflect pathway contributions, initial reaction conditions are essential. These were shown to exist by the following criteria: negligible fractional conversion of substrate to product and no measurable back reaction in deermice having a reversible enzyme (ADH). Thus, calculations from D(V/K) indicate that, even when ADH is present, non-ADH pathways (mostly MEOS) participate significantly in ethanol metabolism at all concentrations tested and play a major role at high levels

Melting point of high-purity germanium stable isotopes

Science.gov (United States)

Gavva, V. A.; Bulanov, A. D.; Kut'in, A. M.; Plekhovich, A. D.; Churbanov, M. F.

2018-05-01

The melting point (Tm) of germanium stable isotopes 72Ge, 73Ge, 74Ge, 76Ge was determined by differential scanning calorimetry. With the increase in atomic mass of isotope the decrease in Tm is observed. The decrease was equal to 0.15 °C per the unit of atomic mass which qualitatively agrees with the value calculated by Lindemann formula accounting for the effect of "isotopic compression" of elementary cell.

Isotope and Hydrochemical Study of Seawater Intrusion into the Aquifers of a Coastal Zone in Cuba

Energy Technology Data Exchange (ETDEWEB)

Dapena, C.; Panarello, H. O.; Ducos, E. I.; Marban, L. [Instituto de Geocronologia y Geologia Isotopica (INGEIS, CONICET -UBA), Buenos Aires (Argentina); Peralta Vital, J. L.; Gil Castillo, R.; Leyva Bombuse, D. [Centro de Proteccion e Higiene de las Radiaciones (CPHR), La Habana (Cuba); Valdez, L. [Empresa de Investigaciones y Proyectos Hidraulicos Habana, La Habana (Cuba); Olivera Acosta, J. [Instituto de Geofisica y Astronomia. La Habana (Cuba)

2013-07-15

The Artemisa-Quivican Basin is located in the southern sector of the province of Havana, Cuba. This basin contains the most important aquifer of Havana province. It has a length of nearly 120 km and is 25 km in width. Recharge depends on the precipitation regime and rain infiltrates in a considerable proportion due to the intense development of karstic features. This aquifer is used for water supply to population, industry, and irrigation and is affected by over-exploitation and risk of contamination by saline sea intrusion. The main objective of this study is the isotope and chemical characterization of the aquifer and the delimitation of the area influenced by saline intrusion. Groundwater and river water are of the calcium bicarbonate type except those with evidence of mixture with saline water. Groundwater exhibits a variable proportion of mixture with seawater, indicating the presence of the saline intrusion. (author)

Mechanism of Microwave-Assisted Pyrolysis of Glucose to Furfural Revealed by Isotopic Tracer and Quantum Chemical Calculations.

Science.gov (United States)

Bao, Liwei; Shi, Lei; Luo, Hu; Kong, Lingzhao; Li, Shenggang; Wei, Wei; Sun, Yuhan

2017-08-10

Glucose labeled with 13 C or 18 O was used to investigate the mechanism of its conversion into furfural by microwaveassisted pyrolysis. The isotopic content and location in furfural were determined from GC-MS and 13 C NMR spectroscopic measurements and data analysis. The results suggest that the carbon skeleton in furfural is mainly derived from C1 to C5 of glucose, whereas the C of the aldehyde group and the O of the furan ring in furfural primarily originate from C1 and O5 of glucose, respectively. For the first time, the source of O in the furan ring of furfural was elucidated directly by experiment, providing results that are consistent with predictions from recent quantum chemical calculations. Moreover, further theoretical calculations indicate substantially lower energy barriers than previous predictions by considering the potential catalytic effect of formic acid, which is one of the pyrolysis products. The catalytic role of formic acid is further confirmed by experimental evidence. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

New approximations for the interference term applied to the calculation of scattering cross section of the {sup 238} U isotope

Energy Technology Data Exchange (ETDEWEB)

Palma, Daniel Artur Pinheiro [Centro Federal de Educacao Tecnologica de Quimica de Nilopolis, RJ (Brazil)]. E-mails: dpalma@cefeteq.br; Martinez, Aquilino Senra; Goncalves, Alessandro C. [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Coordenacao dos Programas de Pos-Graduacao em Engenharia (COPPE). Programa de Engenharia Nuclear]. E-mail: agoncalves@con.ufrj.br; aquilino@lmp.ufrj.br

2008-07-01

The calculation of the Doppler broadening function and the interference term are very important in the generation of nuclear data. Recent papers have proposed analytical formulations for both functions and, despite their being simple and precise, they contain the error function with a complex argument. With the intention of simplifying the mathematical treatment two approximations are proposed in this paper. The first one consists of using an expansion in the form of series to treat the error function. The other approximation is based on simplifications in the differential equations that govern the Doppler broadening function. For validation purpose the result obtained is compared to the one obtained in the calculation of the cross sections for isotope {sup 238}U for different resonances. Results obtained have proved satisfactory from the standpoint of accuracy. (author)

Generalized-seniority scheme in light Sn isotopes

International Nuclear Information System (INIS)

Sandulescu, N.; Blomqvist, J.; Liotta, R.J.; Engeland, T.; Hjorth-Jensen, M.; Holt, A.; Osnes, E.

1998-01-01

In the last years the region of light Sn isotopes has been intensively investigated both from experimental and theoretical perspectives. The main goal was to study the excitation mechanisms around the exotic isotope 100 Sn, the heaviest symmetric double magic nucleus which may exist. The simplest approach in analysing the spectra of light tin isotopes is to consider 100 Sn as an inert core and to treat only neutron degrees of freedom in the valence shell N = 50-82. Extensive shell model calculations have been performed on this line. On the other hand, a large part of the light Sn isotopes spectra could be rather well described in terms of simple quasiparticle excitations. Therefore one expects that at least a part of the low-lying states in this region are well approximated in shell-model subspaces with reduced dimensions. An alternative in truncating the shell model space to low-dimensions is the generalized seniority scheme (GSEN). The aim of this letter is to analyse the accuracy of the GSEN scheme for the case of light tin isotopes. In the present calculations we use a microscopically derived interaction. The yrast generalized seniority states are compared with the corresponding shell model states for the case of the tin isotopes 104-112 Sn. For most of the states that agreement is within 100 keV, although the SM space is drastically truncated. For instance, in 110 Sn the number of SM basis states 2 + is 86990, compared with 9 in the case of GSEN. The seniority two states correspond to the particle-number projected QRPA (Quasiparticle Random Phase Approximation) states. One expects the quasiparticle approximations to break down when the number of active nucleons is small. In order to investigate this in the case of light Sn isotopes, we calculated also the energies predicted by QRPA. The agreement of the QRPA with the exact SM result is impressive, even in the case of only few extra-core neutrons. This is due to the large pairing correlations in the high

Isotopes to Study the coastal aquifer plain, Cap Bon, Tunisia

International Nuclear Information System (INIS)

Ben Hamouda, M. F.; Zouari, Kamel; Tarhouni, J.; Gaye, C.B.; Oueslati, M.N.

2005-01-01

The study area is located in the northeastern part of Tunisia about 60 km south of the Tunis city. It is bounded by the Gulf of Haematite in the East, Djebel Sidi Aberahmane in the West, The town of Nabeul in the south and the area of the town Kelibia in the north. The landscape is a coastal plain slightly sloping (3%) towards the sea. The groundwater of the Oriental coast aquifer system occurs mainly at two levels, a shallow aquifer up to depths of about 50 m whose reservoir is consisted by sediments of the Plio quaternary and a deep aquifer between about 150 and 400 m located in the sand stone formations of Miocene of the anticline of Djebel Sidi Abderrahmene. The climate of the region is semi-arid to sub-humid and of Mediterranean type. There are no perennial rivers in this region; but intense storms occasionally cause surface runoff, which is discharged by the oueds. The study is related to a technical cooperation project with the International Atomic Energy Agency, Vienna, Austria, aimed at the use of isotope techniques to study the seawater intrusion into the coastal aquifers of Cap Bon in Tunisia. In this regard, a better understanding of the recharge and flow regime as well as the origin or salinity of the groundwater was required. To reach this goal, isotope and geochemical investigations were carried out. Water samples were taken from wells, boreholes from deep and shallow aquifer of the Oriental coastal aquifer located between Beni Khiar in the south and Kelibia in the north. The samples were analysed for their chemical and isotopic compositions (18O, 2H, 3H, 13C, 14C, 34S). In the following, the results of these analyses are presented and discussed in terms of the recharge and flow regime of the groundwater and the origin and evolution of its salinity. The results of geochemical and isotopic studies have shown that the groundwater is very eterogeneous and suggest the aquifer is replenished by recent water coming from direct infiltration from rain. At

Modelling soil salinity in Oued El Abid watershed, Morocco

Science.gov (United States)

Mouatassime Sabri, El; Boukdir, Ahmed; Karaoui, Ismail; Arioua, Abdelkrim; Messlouhi, Rachid; El Amrani Idrissi, Abdelkhalek

2018-05-01

Soil salinisation is a phenomenon considered to be a real threat to natural resources in semi-arid climates. The phenomenon is controlled by soil (texture, depth, slope etc.), anthropogenic factors (drainage system, irrigation, crops types, etc.), and climate factors. This study was conducted in the watershed of Oued El Abid in the region of Beni Mellal-Khenifra, aimed at localising saline soil using remote sensing and a regression model. The spectral indices were extracted from Landsat imagery (30 m resolution). A linear correlation of electrical conductivity, which was calculated based on soil samples (ECs), and the values extracted based on spectral bands showed a high accuracy with an R2 (Root square) of 0.80. This study proposes a new spectral salinity index using Landsat bands B1 and B4. This hydro-chemical and statistical study, based on a yearlong survey, showed a moderate amount of salinity, which threatens dam water quality. The results present an improved ability to use remote sensing and regression model integration to detect soil salinity with high accuracy and low cost, and permit intervention at an early stage of salinisation.

The 10B(n,α)7Li reaction in PWR coolants: calculations of the effect on coolant pH and on decreases in 10B isotopic fractions

International Nuclear Information System (INIS)

Polley, M.V.

1988-07-01

Boron is used as a chemical shim in PWRs for reactivity control and is added in the form of boric acid to the primary coolant. The 10 B(n,α) 7 Li reaction leads to a continuous increase in 7 Li in the primary coolant and to a continuous decrease in 10 B the isotope of boron responsible for control of reactivity. The rate of increase in coolant pH due to 7 Li production is calculated for the Sizewell 'B' PWR to enable judgements to be made on the frequency of sampling and removal of lithium required to maintain the pH of the primary coolant within the desired limits. Calculations are contrasted for the cases of natural boron and 100% 10 B chemical shims, for both a normal cycle and an extended 18 month cycle. Calculations of 10 B depletion over 30 years of operation as a function of the quantity of boron discharged to waste are also presented. 10 B isotopic fractions are calculated for the reactor coolant (RC), boric acid tanks (BATs) and refuelling water storage tank (RWST) assuming rapid mixing of BAT and RC boron for tritium control and other reasons. Such predictions enable assessments of the reactor physics implications of 10 B consumption to be made. (author)

Geochemical and Isotopic Characteristics of Quaternary Aquifer in Sohag District, Upper Egypt

International Nuclear Information System (INIS)

Ahmed, M.A.

2008-01-01

Thc Nile River valley represent one of the most important regions for agriculture and land reclamation in our area. Environmental isotopes and hydrochemical compositions in conjunction with geological and hydrogeological data were used to define chemical characteristics, sources of salinity, ground water origin and the possible recharge sources to the Nile Valley aquifer in Sohag district, Upper Egypt. The total dissolved solids of the ground water samples have higher values (445-7828 mg/L) than surface water (291-348 mg/L). The ground water in the Nile flood plain is very similar to that of the river water except at the margins of the basin. This ground water contains isotopic contents comparable to the river Nile with low TDS. The change of water quality at the old alluvium plain could be due to extensive use of fertilizers to improve soil characteristics in new reclamation area. Mineral saturation indices suggest that the dissolution of evaporites and halite is significant in the ground water and responsible for most of the ground water salinization. The relationships between Na + ,Cl - , Ca 2+ , Mg 2+ ,HCO 3 - and SO 4 2- show that complex geochemical processes control the chemical history of ground water: (I) continuous dissolution of evaporites and halite and precipitation of carbonate rocks, (2) cation exchange between ground water and clay minerals, (3) excessive use of fertilizers rich in MgSO 4 in the reclamation projects. The isotopic contents of surface water raged from 2.03 to 2.93%0 for δ 18 O, from 15.3 to 28.4%0 for δ 3 H, and from 4.6 to 7.8 TU for tritium while the isotopic contents of ground water ranged from -8,41 to 3,86% o for δ 18 O, from -67.8 to 29.9%0 for δ 2 H, and from 0.5 to 11.3 TU for tritium. The isotopic data reveals that the rechargability of this water is attributed to Nile flood water which was depleted in its isotopic content. Significant contribution from the palaeowater, which stored in the Nubia sandstone aquifer system

Chlorine isotope fractionation during supergene enrichment of copper

Science.gov (United States)

Reich, M.; Barnes, J.; Barra, F.; Milojevic, C.; Drew, D.

2017-12-01

Supergene enrichment of Cu deposits in the Atacama Desert has played a critical role in making this the prime Cu-producing province of the world. The Cu-hydroxychloride atacamite is a major component of supergene zones in this region whereas in similar deposits elsewhere it is rare. Atacamite requires saline water to form and dissolves rapidly when exposed to fresh, meteoric water. Previous chlorine stable isotope data [1] for atacamite mineralization at the Radomiro Tomic, Chuquicamata and Mina Sur Cu deposits show δ37Cl values that range from -0.1 to +0.2‰, indicating a similar nonmagmatic source for the introduction of chloride. However, distal atacamite mineralization on the periphery of these orebodies show more fractionated and lighter δ37Cl values (-3.2 to -0.1‰). Although little disagreement currently exists about the involvement of saline groundwater during the formation of atacamite [2], no δ37Cl data are currently available for atacamite within a single deposit and/or supergene enrichment profile that allow explaining the aforementioned differences in the observed δ37Cl values. Furthermore, no experimental data for chlorine isotope fractionation between Cu-hydroxychloride minerals and water exist that help evaluate possible mechanisms of fractionation along the groundwater flow path. Here we present a new database that combines detailed mineralogical observations with δ37Cl data of atacamite along a thick ( 100 m) supergene enrichment profile at the Barreal Seco IOCG deposit in the Atacama Desert of northern Chile. Chlorine stable isotope data of atacamite vary between -0.62 and +2.1 ‰ and show a well-defined trend where δ37Cl values progressively decrease (become lighter) with depth. These data, when combined with new experimental determinations of chlorine isotope fractionation between atacamite and water, point to changes triggered by the progressive deepening of groundwater tables during Andean uplift and the extreme desiccation of

Water sources accessed by arid zone riparian trees in highly saline environments, Australia.

Science.gov (United States)

Costelloe, Justin F; Payne, Emily; Woodrow, Ian E; Irvine, Elizabeth C; Western, Andrew W; Leaney, Fred W

2008-05-01

The flow regimes of arid zone rivers are often highly variable, and shallow groundwater in the alluvial aquifers can be very saline, thus constraining the availability and quality of the major water sources available to riparian trees-soil water, shallow groundwater and stream water. We have identified water sources and strategies used by riparian trees in more highly saline and arid conditions than previously studied for riparian trees of arid zone rivers. Our research focused on the riparian species Eucalyptus coolabah, one of the major riparian trees of ephemeral arid zone rivers in Australia. The water sources available to this riparian tree were examined using delta(18)O isotope data from xylem, soil water, groundwater and surface water. Additionally, soil chloride and matric potential data were used to infer zones of water availability for root uptake. Despite the saline conditions, the trees used a mixture of soil water and groundwater sources, but they did not use surface water directly. The study identified three strategies used to cope with typically high groundwater and soil water salinities. Firstly, the trees preferentially grow in zones of most frequent flushing by infiltrating streamflow, such as the bank-tops of channels. Secondly, the trees limit water use by having low transpiration rates. Thirdly, the trees are able to extract water at very low osmotic potentials, with water uptake continuing at chloride concentrations of at least 20,000-30,000 mg L(-1).

Magnesium isotope fractionation in cation-exchange chromatography

International Nuclear Information System (INIS)

Oi, T.; Yanase, S.; Kakihana, H.

1987-01-01

Band displacement chromatography of magnesium has been carried out successfully for the purpose of magnesium isotope separation by using a strongly acidic cation-exchange resin and the strontium ion as the replacement ion. A small but definite accumulation of the heavier isotopes ( 25 Mg, 26 Mg) has been observed at the front parts of the magnesium chromatograms. The heavier isotopes have been fractionated preferentially into the solution phase. The single-stage separation factors have been calculated for the 25 Mg/ 24 Mg and 26 Mg/ 24 isotopic pairs at 25 0 C. The reduced partition function ratios of magnesium species involved in the present study have been estimated

Application of stable isotopes and isotope pattern deconvolution-ICPMS to speciation of endogenous and exogenous Fe and Se in rats

International Nuclear Information System (INIS)

Gonzalez Iglesias, H.; Fernandez-Sanchez, M.L.; Garcia Alonso, J.I.; Lopez Sastre, J.B.; Sanz-Medel, A.

2009-01-01

Full text: Enriched stable isotopes are crucial to study essential trace element metabolism (e.g. Se, Fe) in biological systems. Measuring isotope ratios by ICPMS and using appropriate mathematical calculations, based on isotope pattern deconvolution (IPD) may provide quantitative data about endogenous and exogenous essential or toxic elements and their metabolism. In this work, IPD was applied to explore the feasibility of using two Se (or Fe) enriched stable isotopes, one as metabolic tracer and the other as quantitation tracer, to discriminate between the endogenous and supplemented Se (or Fe) species in rat fluids by collision cell ICPMS coupled to HPLC separation. (author)

Stable isotope deltas: Tiny, yet robust signatures in nature

Science.gov (United States)

Brand, Willi A.; Coplen, Tyler B.

2012-01-01

Although most of them are relatively small, stable isotope deltas of naturally occurring substances are robust and enable workers in anthropology, atmospheric sciences, biology, chemistry, environmental sciences, food and drug authentication, forensic science, geochemistry, geology, oceanography, and paleoclimatology to study a variety of topics. Two fundamental processes explain the stable isotope deltas measured in most terrestrial systems: isotopic fractionation and isotope mixing. Isotopic fractionation is the result of equilibrium or kinetic physicochemical processes that fractionate isotopes because of small differences in physical or chemical properties of molecular species having different isotopes. It is shown that the mixing of radioactive and stable isotope end members can be modelled to provide information on many natural processes, including 14C abundances in the modern atmosphere and the stable hydrogen and oxygen isotopic compositions of the oceans during glacial and interglacial times. The calculation of mixing fractions using isotope balance equations with isotope deltas can be substantially in error when substances with high concentrations of heavy isotopes (e.g. 13C, 2H, and 18O ) are mixed. In such cases, calculations using mole fractions are preferred as they produce accurate mixing fractions. Isotope deltas are dimensionless quantities. In the International System of Units (SI), these quantities have the unit 1 and the usual list of prefixes is not applicable. To overcome traditional limitations with expressing orders of magnitude differences in isotope deltas, we propose the term urey (symbol Ur), after Harold C. Urey, for the unit 1. In such a manner, an isotope delta value expressed traditionally as−25 per mil can be written as−25 mUr (or−2.5 cUr or−0.25 dUr; the use of any SI prefix is possible). Likewise, very small isotopic differences often expressed in per meg ‘units’ are easily included (e.g. either+0.015 ‰ or+15 per meg

Isotopic study of the ''Laguna Mar Chiquita'', Cordoba, Argentina and its hydrogeological and paleoclimatological implications

International Nuclear Information System (INIS)

Dapena, C.; Panarello, H.O.

2001-01-01

This work presents the results obtained during the first stage of the investigations carried out in the Mar Chiquita lake (Cordoba Province, Argentine Republic) within the framework of the Coordinated Research Programme (CRP) on ''Isotope Techniques in Lake Dynamics Investigations'' of the International Atomic Energy Agency. The main objectives are to contribute to the study of this huge water body that in the past two decades increased its size almost three folds, to establish its water balance and to asses the influence of the climatic changes on the water budget. This water body is the final receptacle of a large closed basin formed mainly by the rivers Dulce, Suquia and Xanaes. During 1890-1973 it occupied 1800 to 2000 km 2 with a salinity of 310-250 g/L. At present, it has around 5000 km 2 , a maximum depth of 10-12 m and a salinity rounding 42 g/L. The changes in salinity and size are related to an increase in precipitation which, at the same time, depends on different palaeoclimatic conditions. From a scientific point of view it is also important to study the lake hydrological balance, its groundwater input and output as well as the evaporation rate and the mean residence time. These latter considerations are the object of the present isotopic research. Future studies will consider a paleoclimatic approach. (author)

Coupled sulfur isotopic and chemical mass transfer modeling: Approach and application to dynamic hydrothermal processes

International Nuclear Information System (INIS)

Janecky, D.R.

1988-01-01

A computational modeling code (EQPSreverse arrowS) has been developed to examine sulfur isotopic distribution pathways coupled with calculations of chemical mass transfer pathways. A post processor approach to EQ6 calculations was chosen so that a variety of isotopic pathways could be examined for each reaction pathway. Two types of major bounding conditions were implemented: (1) equilibrium isotopic exchange between sulfate and sulfide species or exchange only accompanying chemical reduction and oxidation events, and (2) existence or lack of isotopic exchange between solution species and precipitated minerals, parallel to the open and closed chemical system formulations of chemical mass transfer modeling codes. All of the chemical data necessary to explicitly calculate isotopic distribution pathways is generated by most mass transfer modeling codes and can be input to the EQPS code. Routines are built in to directly handle EQ6 tabular files. Chemical reaction models of seafloor hydrothermal vent processes and accompanying sulfur isotopic distribution pathways illustrate the capabilities of coupling EQPSreverse arrowS with EQ6 calculations, including the extent of differences that can exist due to the isotopic bounding condition assumptions described above. 11 refs., 2 figs

Management scenarios for the Jordan River salinity crisis

Science.gov (United States)

Farber, E.; Vengosh, A.; Gavrieli, I.; Marie, Amarisa; Bullen, T.D.; Mayer, B.; Holtzman, R.; Segal, M.; Shavit, U.

2005-01-01

Recent geochemical and hydrological findings show that the water quality of the base flow of the Lower Jordan River, between the Sea of Galilee and the Dead Sea, is dependent upon the ratio between surface water flow and groundwater discharge. Using water quality data, mass-balance calculations, and actual flow-rate measurements, possible management scenarios for the Lower Jordan River and their potential affects on its salinity are investigated. The predicted scenarios reveal that implementation of some elements of the Israel-Jordan peace treaty will have negative effects on the Jordan River water salinity. It is predicted that removal of sewage effluents dumped into the river (???13 MCM/a) will significantly reduce the river water's flow and increase the relative proportion of the saline groundwater flux into the river. Under this scenario, the Cl content of the river at its southern point (Abdalla Bridge) will rise to almost 7000 mg/L during the summer. In contrast, removal of all the saline water (16.5 MCM/a) that is artificially discharged into the Lower Jordan River will significantly reduce its Cl concentration, to levels of 650-2600 and 3000-3500 mg/L in the northern and southern areas of the Lower Jordan River, respectively. However, because the removal of either the sewage effluents or the saline water will decrease the river's discharge to a level that could potentially cause river desiccation during the summer months, other water sources must be allocated to preserve in-stream flow needs and hence the river's ecosystem. ?? 2005 Elsevier Ltd. All rights reserved.

Rock-matrix diffusion in transport of salinity. Implementation in CONNECTFLOW

International Nuclear Information System (INIS)

Hoch, A.R.; Jackson, C.P.

2004-07-01

One of the programs used for modelling groundwater flow in Swedish rocks for SKB is CONNECTFLOW, which combines the facilities of the programs NAMMU for modelling continuum porous-medium models and NAPSAC for modelling discrete fracture-networks. The version of CONNECTFLOW current at the start of the work described here did not have a capability to model rock-matrix diffusion for saline flows in continuum porous-medium models of fractured rocks. Possible approaches for implementing such an option were evaluated and then the approach that was considered to be the most suitable was implemented and tested and then used in calculations for a realistic example. Three main approaches for representing diffusion in the rock matrix were considered: the use of a numerical finite-difference scheme, an approach based on the use of Laplace transforms, and a so-called 'hybrid' approach which combines a series solution that gives a good representation at long times with an inverse square-root form that gives a good representation at small times. The finite-difference approach is the most flexible of the approaches considered. In particular, it is the only approach that can deal with the case in which, at each location in the continuum representing the fractures, the groundwater density varies within the rock matrix. The Laplace transform approach and the hybrid approach treat the diffusion in the rock matrix exactly, whereas the finite-difference approach involves discretisation errors. In particular, the unit response function is significantly in error for the first few time steps. The method that was considered to be the most appropriate to implement initially in CONNECTFLOW for SKB was the hybrid method. The algorithm was used to carry out calculations for a large site-scale model, based on the version 1.1 model of the Forsmark site in Sweden. Calculations of the evolution of the groundwater flow system from conditions 10,000 years ago to the present were carried out. The

Management of ground water using isotope techniques

International Nuclear Information System (INIS)

Romani, Saleem

2004-01-01

Ground water play a major role in national economy and sustenance of life and environment. Prevalent water crisis in India includes falling water table, water quality deterioration, water logging and salinity. Keeping in view the increasing thrust on groundwater resources and the present scenario of availability vis-a vis demand there is a need to reorient our approach to ground water management. The various ground water management options require proper understanding of ground water flow system. Isotopes are increasingly being applied in hydrogeological investigations as a supplementary tool for assessment of aquifer flow and transport characteristics. Isotope techniques coupled with conventional hydrogeological and hydrochemical methods can bring in greater accuracy in the conceptualization of hydrogeological control mechanism. The use of isotope techniques in following areas can certainly be of immense help in implementing various ground water management options in an efficient manner. viz.Interaction between the surface water - groundwater systems to plan conjunctive use of surface and ground water. Establishing hydraulic interconnections between the aquifers in a multi aquifer system. Depth of circulation of water and dating of ground water. Demarcating ground water recharge and discharge areas. Plan ground water development in coastal aquifers to avoid sea water ingress. Development of flood plain aquifer. (author)

Molecular modeling study of lithium isotopic separation by crown-ethers in ethanol

International Nuclear Information System (INIS)

Dehez, F.

2002-01-01

The isotopic separation of lithium ion isotopes is studied at the CEA in Pierrelatte using a liquid chromatography technique. Exchange systems are composed by crown-ethers grafted on silica (12C4, 15C5, B15C5, DB15C5, 18C6, B18C6). Lithium is introduced as a salt melted in ethanol. This work concerns the theoretical study of lithium isotopic exchange reactions with those systems. After a brief presentation of isotope separation techniques and isotopic effects (Chap.I), we describe the methods of theoretical chemistry used in this work (Chap. II). In chapter III, we test AM1 and PM3 semi-empirical methods for the treatment of Li + /crown-ether species. Then, we calculate isotopic separation factors via ab initio and semi-empirical calculations for the exchange reactions in vacuum. The different crown-ethers are considered with and without graftings arms. Studies of exchange reactions in ethanol are presented in chapter IV. First, each species of the reaction are solvated by a few ethanol molecules. Isotopic separation factors calculated show a large effect of the solvent on the exchange reaction. The effect of the grafting arm has been investigated using hybrid quantum mechanics/molecular mechanics (QM/MM) molecular dynamics for species with the 12C4. Trajectories have been generated successively with 7 Li and 6 Li. Atomic velocity autocorrelation functions have allowed the access to vibrational frequencies necessary to calculate isotopic separation factors. The last chapter is devoted to methodological developments made during this Ph.D. We propose an approach to treat long range electrostatic interactions in hybrid QM/MM method, relying on a lattice summation technique. (author) [fr

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

Science.gov (United States)

Ryb, U.; Eiler, J. M.

2017-12-01

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

Deciphering the modern calcification depth of Globigerina bulloides in the southwestern Indian Ocean from its oxygen isotopic composition

Digital Repository Service at National Institute of Oceanography (India)

Saraswat, R.; Khare, N.

-fit results. Similarly, the estimated seawater salinity was calculated using the seawater delta sup(18)O calculated from G. bulloides delta sup(18)O, and measured seawater temperature taken from the Levitus database. A comparison of seawater salinity...

Exposure calculations for the FRG isotopic heat source project environmental assessment

International Nuclear Information System (INIS)

Metcalf, I.L.

1997-01-01

The report documents the maximum exposure for transfer of the Federal Republic of Germany (FRG) Isotopic Heat Sources from the 324 Building and placed in interim storage at the Central Waste Complex (CWC). These results are to be reported in the Environmental Assessment DOE-EA- 1 21 1

Recent results on neutron rich tin isotopes by laser spectroscopy

CERN Document Server

Roussière, B; Crawford, J E; Essabaa, S; Fedosseev, V; Geithner, W; Genevey, J; Girod, M; Huber, G; Horn, R; Kappertz, S; Lassen, J; Le Blanc, F; Lee, J K P; Le Scornet, G; Lettry, Jacques; Mishin, V I; Neugart, R; Obert, J; Oms, J; Ouchrif, A; Peru, S; Pinard, J; Ravn, H L; Sauvage, J; Verney, D

2001-01-01

Laser spectroscopy measurements have been performed on neutron rich tin isotopes using the COMPLIS experimental setup. The nuclear charge radii of the even-even isotopes from A=108 to 132 are compared to the results of macroscopic and microscopic calculations. The improvements and optimizations needed to perform the isotope shift measurement on $^{134}$Sn are presented.

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

International Nuclear Information System (INIS)

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

2011-01-01

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

Comparison of force fields and calculation methods for vibration intervals of isotopic H+3 molecules

International Nuclear Information System (INIS)

Carney, G.D.; Adler-Golden, S.M.; Lesseski, D.C.

1986-01-01

This paper reports (a) improved values for low-lying vibration intervals of H + 3 , H 2 D + , D 2 H + , and D + 3 calculated using the variational method and Simons--Parr--Finlan representations of the Carney--Porter and Dykstra--Swope ab initio H + 3 potential energy surfaces, (b) quartic normal coordinate force fields for isotopic H + 3 molecules, (c) comparisons of variational and second-order perturbation theory, and (d) convergence properties of the Lai--Hagstrom internal coordinate vibrational Hamiltonian. Standard deviations between experimental and ab initio fundamental vibration intervals of H + 3 , H 2 D + , D 2 H + , and D + 3 for these potential surfaces are 6.9 (Carney--Porter) and 1.2 cm -1 (Dykstra--Swope). The standard deviations between perturbation theory and exact variational fundamentals are 5 and 10 cm -1 for the respective surfaces. The internal coordinate Hamiltonian is found to be less efficient than the previously employed ''t'' coordinate Hamiltonian for these molecules, except in the case of H 2 D +

Assessing Salinity in Cotton and Tomato Plants by Using Reflectance Spectroscopy

Science.gov (United States)

Goldshleger, Naftaly

2016-04-01

Irrigated lands in semi-arid and arid areas are subjected to salinization processes. An example of this phenomenon is the Jezreel Valley in northern Israel where soil salinity has increased over the years. The increase in soil salinity results in the deterioration of the soil structure and crops damage. In this experiment we quantified the relation between the chemical and spectral features of cotton and tomato plants and their mutual relationship to soil salinity. The experiment was carried out as part of ongoing research aiming to detect and monitor saline soils and vegetation by combining different remote sensing methods. The aim of this study was to use vegetation reflectance measurements to predict foliar Cl and Na concentration and assess salinity in the soil and in vegetation by their reflectance measurements. The model developed for determining concentrations of chlorine and sodium in tomato and cotton produced good results ( R2 = 0.92 for sodium and 0.85 for chlorine in tomato and R2 = 0.84 for sodium and 0.82 for chlorine in cotton). Lately, we extend the method to calculate vegetation salinity, by doing correlation between the reflectance slopes of the tested crops CL and Na from two research areas. The developed model produced a good results for all the data (R2=0.74) Our method can be implemented to assess vegetation salinity ahead of planting, and developed as a generic tool for broader use for agriculture in semi-arid regions. In our opinion these results show the possibility of monitoring for a threshold level of salinity in tomato and cotton leaves so remedial action can be taken in time to prevent crop damage. Our results strongly suggest that future imaging spectroscopy remote sensing measurements collected by airborne and satellite platforms could measure the salinity of soil and vegetation over larger areas. These results can be the first steps for generic a model which includes more vegetation for salinity measurements.

Use of isotope effects to elucidate enzyme mechanisms

International Nuclear Information System (INIS)

Cleland, W.W.

1982-01-01

The chemical bond breaking steps are normally not rate limiting for enzymatic reactions. However, comparison of deuterium and tritium isotope effects on the same reaction, especially when coupled with 13 C isotope effects for the same step measured with deuterated as well as unlabeled substrates, allows calculation of the intrinsic isotope effects on the bond breaking steps and thus a determination of the commitments to catalysis for the reactants. The variation in observed isotope effects as a function of reactant concentration can be used to determine kinetic mechanisms, while the pH variation of isotope effects can determine the stickiness of the reactants and which portions of the reactant mechanism are pH dependent. Finally the size of primary and secondary intrinsic isotope effects can be used to determine transition state structure

Beyond temperature: Clumped isotope signatures in dissolved inorganic carbon species and the influence of solution chemistry on carbonate mineral composition

Science.gov (United States)

Tripati, Aradhna K.; Hill, Pamela S.; Eagle, Robert A.; Mosenfelder, Jed L.; Tang, Jianwu; Schauble, Edwin A.; Eiler, John M.; Zeebe, Richard E.; Uchikawa, Joji; Coplen, Tyler B.; Ries, Justin B.; Henry, Drew

2015-10-01

;Clumped-isotope; thermometry is an emerging tool to probe the temperature history of surface and subsurface environments based on measurements of the proportion of 13C and 18O isotopes bound to each other within carbonate minerals in 13C18O16O22- groups (heavy isotope ;clumps;). Although most clumped isotope geothermometry implicitly presumes carbonate crystals have attained lattice equilibrium (i.e., thermodynamic equilibrium for a mineral, which is independent of solution chemistry), several factors other than temperature, including dissolved inorganic carbon (DIC) speciation may influence mineral isotopic signatures. Therefore we used a combination of approaches to understand the potential influence of different variables on the clumped isotope (and oxygen isotope) composition of minerals. We conducted witherite precipitation experiments at a single temperature and at varied pH to empirically determine 13C-18O bond ordering (Δ47) and δ18O of CO32- and HCO3- molecules at a 25 °C equilibrium. Ab initio cluster models based on density functional theory were used to predict equilibrium 13C-18O bond abundances and δ18O of different DIC species and minerals as a function of temperature. Experiments and theory indicate Δ47 and δ18O compositions of CO32- and HCO3- ions are significantly different from each other. Experiments constrain the Δ47-δ18O slope for a pH effect (0.011 ± 0.001; 12 ⩾ pH ⩾ 7). Rapidly-growing temperate corals exhibit disequilibrium mineral isotopic signatures with a Δ47-δ18O slope of 0.011 ± 0.003, consistent with a pH effect. Our theoretical calculations for carbonate minerals indicate equilibrium lattice calcite values for Δ47 and δ18O are intermediate between HCO3- and CO32-. We analyzed synthetic calcites grown at temperatures ranging from 0.5 to 50 °C with and without the enzyme carbonic anhydrase present. This enzyme catalyzes oxygen isotopic exchange between DIC species and is present in many natural systems. The two

Salinity dependent hydrogen isotope fractionation in alkenones produced by coastal and open ocean haptophyte algae

NARCIS (Netherlands)

M'boule, D.; Chivall, D.; Sinke-Schoen, D.; Sinninghe Damsté, J.S.; Schouten, S.; van der Meer, M.T.J.

2014-01-01

The hydrogen isotope fractionation in alkenones produced by haptophyte algae is a promising new proxy for paleosalinity reconstructions. To constrain and further develop this proxy the coastal haptophyte Isochrysis galbana and the open ocean haptophyte alga Emiliania huxleyi were cultured at

Implementation of isotope correlation technique for safeguards

International Nuclear Information System (INIS)

Persiani, P.J.; Bucher, R.G.

1989-01-01

The isotopic correlation technique (ICT) is based on the fundamental physics principle that the isotopic compositions of nuclear material in the fuel cycle systems contain information regarding the design and history of nuclear material flow from fuel fabrication, reactor operation, and through input to the reprocessing plant. Isotopic Correlation in conjunction with the gravimetric (or Pu/U) method for mass determination can be developed to provide an independent in-field verification of the reprocessing input accountancy at the dissolver and/or accountancy stage of the reprocessing plant. The Argonne National Laboratory program in isotope correlation techniques is based on three-dimensional reactor physics calculations of characteristic geometries/composition in each reactor class. 10 refs., 1 fig., 3 tabs

Salinity, temperature and density data for the Canadian Beaufort Sea shelf, March 1988

Energy Technology Data Exchange (ETDEWEB)

Hopky, G E; Chiperzak, D B; Lawrence, M J

1988-01-01

This report contains salinity, temperature and density (CTD) data collected in the waters of the Canadian Beaufort Sea Shelf during March 1988. Salinity and temperature profile data were measured using a Guildline Model 8870 probe deployed from the ice surface. Ice thickness was also measured. Density was calculated using salinity and temperature values. CTD profiles were measured at five stations. The maximum depths of profiles measured from the ice surface ranged from 31.2 to 16.8 dbar. Salinity and temperature measurements ranged from 0.35 to 34.83, and -1.87 to 1.08/sup 0/C, respectively. The data presented in this report will assist in the identification and delineation of potential habitat types, as part of the Critical Arctic Estuarine and Marine Habitat Project of the Northern Oil and Gas Program. 5 refs., 7 figs., 6 tabs.

Collinear laser spectroscopy on In isotopes from heavy ion fusion reactions

International Nuclear Information System (INIS)

Ulm, G.

1984-07-01

Indium isotopes 107-111 were produced by 16 O-fusion reactions and investigated in a collinear laser geometry. The hyperfine structure and isotopic shifts are measured and the deduced magnetic dipole moments are in agreement with shell model calculations. The nuclear charge radii are determined from the isotopic shifts. (WL)

The effect of dipolar interaction on the magnetic isotope effect

DEFF Research Database (Denmark)

Mojaza, Matin; Pedersen, Jørgen Boiden; Lukzen, Nikita

2010-01-01

A multi-channel kinetic description is used to study the magnetic isotope effect (MIE) in zero magnetic field. The maximal isotope effect is equal to the number of channels, two for the hyperfine interaction but four for the electron spin dipole–dipole interaction of the intermediate radical pair....... Quantum mechanical calculations agree with these conclusion and show that large MIE may be obtained even in the presence of a strong exchange interaction. The observed magnesium isotope effect on the rate of enzymatic synthesis of adenosine triphosphate (ATP) is approximately 3 implying that the dipolar...... interaction is responsible for the effect. Our calculations provide support for the proposed mechanism....

15N Isotopic Study on Decomposition of Organic Residues Incorporated into Alluvial and Sandy Saline Soils

International Nuclear Information System (INIS)

El-Kholi, A. F.; Galal, Y. G. M.

2004-01-01

Incubation experiment was conducted to study the effect of the nitrogenous fertilizer on the decomposition and mineralization of organic residues (soybean powdered forage) as well as the release of the soil inorganic nitrogen. This technique was carried out using two types of soils, one is alluvial and the other is saline sandy soil collected from Fayoum governorate. Soybean forage has an organic carbon 23.1%, total N 1.6% and C/N ratio 14.4. Regarding the effect of incubation period on the two soil samples, the evolved NH 4 -N was generally reached its highest peak after 30-45 days, in the presence of either the added 15 No3-fertilizer solely or in combination with soybean forage. Reversible trend was occurred with regard to the evolved No3-N. The highest peak of evolved No3-N recorded in unfertilized control, as compared to 15 No3-N treatment, at 30 day incubation period indicated that the addition of labeled mineral fertilizer had appreciably enhanced the immobilization process. Net nitrification revealed that it was the highest in unfertilized control soil where it was significantly decreased in the treated two soil samples. Gross mineralization as affected by the addition of soybean forage in combination with labeled mineral fertilizer had been promoted by 75% in the alluvial soil and by 18% in the sandy saline soil, as compared with the soil samples received 15 No3-fertilizer only. Gross immobilization, in soil samples received 15 No3-fertilizer plus soybean forage had surpassed those received 15 No3-fertilizer only by 16% in the alluvial soil and by 25% in the sandy saline soil. (Authors)

Very fast isotopic and mass balance calculations used for strategic planing of the nuclear fuel cycle

International Nuclear Information System (INIS)

Marguet, S.D.

1993-01-01

Owing to the prevalence in France of nuclear generated electricity, the french utility, EDF focuses much research on fuel cycle strategy. In this context, analysis of scenarios combining problems related to planning and economics, but also reactor physics, necessitate a relatively thorough understanding of fuel response to irradiation. The main purpose of the fuel strategy program codes is to predict mass balance modifications with time for the main actinides involved in the cycle, including the minor actinides associated with the current back end fuel cycle key issues. Considering the large number of calculations performed by a strategy code in an iterative process covering a range of about a hundred years, it was important to develop basic computation modules for both the ''reactor'' and ''fabrication'' items. These had to be high speed routines, but on an accuracy level compatible with the strategy code efficiency. At the end of 1992, the EDF Research and Development Division (EDF/DER) developed a very simple, extremely fast method of calculating transuranian isotope masses. This approach, which resulted in the STRAPONTIN software, considerably increased the scope of the EDF/DER fuel strategy code TIRELIRE without undue impairment of machine time requirements for a scenario. (author). 2 figs., 2 tabs., 3 refs

Inferring coastal processes from regional-scale mapping of 222Radon and salinity: examples from the Great Barrier Reef, Australia

International Nuclear Information System (INIS)

Stieglitz, Thomas C.; Cook, Peter G.; Burnett, William C.

2010-01-01

The radon isotope 222 Rn and salinity in coastal surface water were mapped on regional scales, to improve the understanding of coastal processes and their spatial variability. Radon was measured with a surface-towed, continuously recording multi-detector setup on a moving vessel. Numerous processes and locations of land-ocean interaction along the Central Great Barrier Reef coastline were identified and interpreted based on the data collected. These included riverine fluxes, terrestrially-derived fresh submarine groundwater discharge (SGD) and the tidal pumping of seawater through mangrove forests. Based on variations in the relationship of the tracers radon and salinity, some aspects of regional freshwater inputs to the coastal zone and to estuaries could be assessed. Concurrent mapping of radon and salinity allowed an efficient qualitative assessment of land-ocean interaction on various spatial and temporal scales, indicating that such surveys on coastal scales can be a useful tool to obtain an overview of SGD locations and processes.

Carbon isotopic fractionation in live benthic foraminifera -comparison with inorganic precipitate studies

Energy Technology Data Exchange (ETDEWEB)

Grossmann, E L [University of Southern California, Los Angeles (USA). Dept. of Geological Sciences

1984-07-01

Carbon and oxygen isotopic analyses have been performed on live-stained aragonitic and calcitic benthic foraminifera and dissolved inorganic carbon from the Southern California Borderland to examine carbon isotopic fractionation in foraminifera. Temperature, salinity and pH data have also been collected to permit accurate determination of the delta/sup 13/C of bicarbonate ion and thus aragonite-HCO/sub 3//sup -/ and calcite-HCO/sub 3//sup -/ isotopic enrichment factors (epsilonsub(ar-b) and epsilonsub(cl-b), respectively). Only species which precipitate in /sup 18/O equilibrium have been considered. epsilonsub (ar-b) values based on Hoeglundina elegans range from 1.9 per mille at 2.7 deg C to 1.1 per mille at 9.5 deg C. The temperature dependence of epsilonsub(ar-b) is considerably greater than the equilibrium equation would predict and may be due to a vital effect. The calcitic foraminifera Cassidulina tortuosa, Cassidulina braziliensis, and Cassidulina limbata, Bank and Terrace dwellers, have s

The isotope hydrology of ground waters of the Kalahari, Gordonia

International Nuclear Information System (INIS)

Verhagen, B. Th.

1982-01-01

An intensive hydrological and geophysical survey of fresh water occurance in the Gordonia area, promoted a parallel study of the isotope hydrology and hydrochemistry of both the fresh and saline ground waters of the area. Measurements of 14 C, 3 H, 13 C and 18 O as well of major element hydrochemistry were conducted on numerous samples. Radiocarbon concentrations range from 6 pmc to 111 pmc. Significant tritium is only observed in cases where 14 C concentrations are significantly higher than 90 pmc

Distribution of oxygen isotopes in the water masses of Drake Passage and the South Atlantic

Science.gov (United States)

Meredith, Michael P.; Grose, Katie E.; McDonagh, Elaine L.; Heywood, Karen J.; Frew, Russell D.; Dennis, Paul F.

1999-09-01

Measurements of the ratio of stable isotopes of oxygen (18O and 16O) from samples collected on World Ocean Circulation Experiment sections SR1b (eastern Drake Passage) and A11 (Punta Arenas to Cape Town) are used, together with hydrographic data, to deduce information about the formation and variability of South Atlantic and Southern Ocean water masses. The Drake Passage surface waters south of the Polar Front (PF) are isotopically light (δ18O around -0.4‰) owing to the influence of meteoric waters. The salinity and δ18O of the A11 surface waters yield an apparent freshwater end-member which is much isotopically lighter than the local precipitation, thus advection of these waters from farther south dominates over local effects in determining the surface water properties. The Drake Passage section shows unusual proximity of the two main fronts of the Antarctic Circumpolar Current (the PF and Subantarctic Front (SAF)), and we observe cold, fresh, and isotopically light water derived from the temperature-minimum Winter Water at the SAF. This water is of the correct density to freshen the intermediate water north of the SAF and thus play a role in the formation of the comparatively fresh Antarctic Intermediate Water (AAIW) of the South Atlantic. This confirms the role of Antarctic water in forming the South Atlantic variety of AAIW. Across the A11 section the oxygen isotope and salinity data at the AAIW core show very similar traces, with waters in the Malvinas Current loop showing lowest values of both. At the eastern boundary of the South Atlantic, the input of Red Sea Water from east of South Africa is observed via the presence of anomalously isotopically heavy AAIW. We deduce potentially significant temporal variability in the isotopic composition of Weddell Sea Deep Water (WSDW) by comparing the Drake Passage data to earlier data covering the outflow of the Weddell Sea. The A11 data show WSDW consistent with such variability, indicating that its effects could

Glutathione reductase: solvent equilibrium and kinetic isotope effects

International Nuclear Information System (INIS)

Wong, K.K.; Vanoni, M.A.; Blanchard, J.S.

1988-01-01

Glutathione reductase catalyzes the NADPH-dependent reduction of oxidized glutathione (GSSG). The kinetic mechanism is ping-pong, and we have investigated the rate-limiting nature of proton-transfer steps in the reactions catalyzed by the spinach, yeast, and human erythrocyte glutathione reductases using a combination of alternate substrate and solvent kinetic isotope effects. With NADPH or GSSG as the variable substrate, at a fixed, saturating concentration of the other substrate, solvent kinetic isotope effects were observed on V but not V/K. Plots of Vm vs mole fraction of D 2 O (proton inventories) were linear in both cases for the yeast, spinach, and human erythrocyte enzymes. When solvent kinetic isotope effect studies were performed with DTNB instead of GSSG as an alternate substrate, a solvent kinetic isotope effect of 1.0 was observed. Solvent kinetic isotope effect measurements were also performed on the asymmetric disulfides GSSNB and GSSNP by using human erythrocyte glutathione reductase. The Km values for GSSNB and GSSNP were 70 microM and 13 microM, respectively, and V values were 62 and 57% of the one calculated for GSSG, respectively. Both of these substrates yield solvent kinetic isotope effects greater than 1.0 on both V and V/K and linear proton inventories, indicating that a single proton-transfer step is still rate limiting. These data are discussed in relationship to the chemical mechanism of GSSG reduction and the identity of the proton-transfer step whose rate is sensitive to solvent isotopic composition. Finally, the solvent equilibrium isotope effect measured with yeast glutathione reductase is 4.98, which allows us to calculate a fractionation factor for the thiol moiety of GSH of 0.456

Constraining the origin of the Messinian gypsum deposits using coupled measurement of δ^{18}O$/δD in gypsum hydration water and salinity of fluid inclusions

Science.gov (United States)

Evans, Nicholas P.; Gázquez, Fernando; McKenzie, Judith A.; Chapman, Hazel J.; Hodell, David A.

2016-04-01

We used oxygen and hydrogen isotopes of gypsum hydration water (GHW) coupled with salinity deduced from ice melting temperatures of primary fluid inclusions in the same samples (in tandem with 87Sr/86Sr, δ34S and other isotopic measurements) to determine the composition of the mother fluids that formed the gypsum deposits of the Messinian Salinity Crisis from shallow and intermediate-depth basins. Using this method, we constrain the origin of the Messinian Primary Lower Gypsum (PLG) of the Sorbas basin (Betic foreland) and both the Upper Gypsum (UG) and the Lower Gypsum of the Sicilian basin. We then compare these results to measurements made on UG recovered from the deep Ionian and Balearic basins drilled during DSDP Leg 42A. The evolution of GHW δ18O/δD vs. salinity is controlled by mixing processes between fresh and seawater, coupled with the degree of evaporation. Evaporation and subsequent precipitation of gypsum from fluids dominated by freshwater will result in a depressed 87Sr/86Sr values and different trajectory in δ18O/δD vs. salinity space compared to fluids dominated by seawater. The slopes of these regression equations help to define the end-members from which the fluid originated. For example, salinity estimates from PLG cycle 6 in the Sorbas basin range from 18 to 51ppt, and after correction for fractionation factors, estimated δ18O and δD values of the mother water are low (-2.6 meteoric water during gypsum deposition, while 87Sr/86Sr (0.708942 fall below those expected from the evaporation of seawater alone, the slope of the regression equation is similar to that of seawater evaporation. This implies that there is a change up-section from a dominantly marine environment in cycle 2 to a greater influence of meteoric water in cycle 6. The UG from the Sicilian basin display greater δ18O/δD values (2.9 meteoric water that subsequently underwent intense evaporation. This observation concurs with the low values of 87Sr/86Sr from the same UG

Saline groundwater in crystalline bedrock

International Nuclear Information System (INIS)

Lampen, P.

1992-11-01

The State-of-art report describes research made on deep saline groundwaters and brines found in crystalline bedrock, mainly in site studies for nuclear waste disposal. The occurrence, definitions and classifications of saline groundwaters are reviewed with a special emphasis on the different theories concerning the origins of saline groundwaters. Studies of the saline groundwaters in Finland and Sweden have been reviewed more thoroughly. Also the mixing of different bodies of groundwaters, observations of the contact of saline groundwaters and permafrost, and the geochemical modelling of saline groundwaters as well as the future trends of research have been discussed. (orig.)

Triple oxygen isotope systematics of structurally bonded water in gypsum

Science.gov (United States)

Herwartz, Daniel; Surma, Jakub; Voigt, Claudia; Assonov, Sergey; Staubwasser, Michael

2017-07-01

The triple oxygen isotopic composition of gypsum mother water (gmw) is recorded in structurally bonded water in gypsum (gsbw). Respective fractionation factors have been determined experimentally for 18O/16O and 17O/16O. By taking previous experiments into account we suggest using 18αgsbw-gmw = 1.0037; 17αgsbw-gmw = 1.00195 and θgsbw-gmw = 0.5285 as fractionation factors in triple oxygen isotope space. Recent gypsum was sampled from a series of 10 ponds located in the Salar de Llamara in the Atacama Desert, Chile. Total dissolved solids (TDS) in these ponds show a gradual increase from 23 g/l to 182 g/l that is accompanied by an increase in pond water 18O/16O. Gsbw falls on a parallel curve to the ambient water from the saline ponds. The offset is mainly due to the equilibrium fractionation between gsbw and gmw. However, gsbw represents a time integrated signal biased towards times of strong evaporation, hence the estimated gmw comprises elevated 18O/16O compositions when compared to pond water samples taken on site. Gypsum precipitation is associated with algae mats in the ponds with lower salinity. No evidence for respective vital effects on the triple oxygen isotopic composition of gypsum hydration water is observed, nor are such effects expected. In principle, the array of δ18Ogsbw vs. 17Oexcess can be used to: (1) provide information on the degree of evaporation during gypsum formation; (2) estimate pristine meteoric water compositions; and (3) estimate local relative humidity which is the controlling parameter of the slope of the array for simple hydrological situations. In our case study, local mining activities may have decreased deep groundwater recharge, causing a recent change of the local hydrology.

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.

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

International Nuclear Information System (INIS)

Deng Yamin; Wang Yanxin; Ma Teng

2009-01-01

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

Uranium in open ocean: concentration and isotopic composition

International Nuclear Information System (INIS)

Ku, T.L.; Knauss, K.G.; Mathieu, G.G.

1977-01-01

Uranium concentrations and 234 U/ 238 U activity ratios have been determined in 63 seawater samples (nine vertical profiles) from the Atlantic, and Pacific, and Arctic, and the Antarctic oceans, using the alpha-spectrometric method for their determinations. Correlation between uranium and salinity is well manifested by the data from the Arctic and the Antarctic oceans, but such a relation cannot be clearly defined with the +-(1 to 2)% precision of uranium measurements for the Atlantic and Pacific data. At the 95% confidence level: (1) the uranium/salinity ratio is (9.34 + - 0.56) x 10 -8 g/g for the seawater analyzed with salinity ranging from 30.3 to 36.2 per thousand; the uranium concentration of seawater of 35 per thousand salinity is 3.3 5 + - 0.2 μ g l -1 ; (2) the 234 U/ 238 U activity ratio is 1.14 +- 0.03. Uranium isotopes in interstitial waters of the Pacific surface sediments analyzed do not show large concentration differences across the sediment-water interface as suggested by previous measurements. Current estimations of the average world river uranium concentration (0.3 to 0.6 μ g l -1 ) and 234 U/ 238 U ratio (1.2 to 1.3) and of the diffusional 234 U influx from sediments 0.3 dpm cm -2 10 -3 yr -1 ) are essentially consistent with a model which depicts a steady state distribution of uranium in the ocean. However, the 0.3 to 0.6 μ g l -1 value for river uranium may be an upper limit estimate. (author)

Beyond temperature: Clumped isotope signatures in dissolved inorganic carbon species and the influence of solution chemistry on carbonate mineral composition

Science.gov (United States)

Tripati, Aradhna K.; Hill, Pamela S.; Eagle, Robert A.; Mosenfelder, Jed L.; Tang, Jianwu; Schauble, Edwin A.; Eiler, John M.; Zeebe, Richard E.; Uchikawa, Joji; Coplen, Tyler B.; Ries, Justin B.; Henry, Drew

2015-01-01

“Clumped-isotope” thermometry is an emerging tool to probe the temperature history of surface and subsurface environments based on measurements of the proportion of 13C and 18O isotopes bound to each other within carbonate minerals in 13C18O16O22- groups (heavy isotope “clumps”). Although most clumped isotope geothermometry implicitly presumes carbonate crystals have attained lattice equilibrium (i.e., thermodynamic equilibrium for a mineral, which is independent of solution chemistry), several factors other than temperature, including dissolved inorganic carbon (DIC) speciation may influence mineral isotopic signatures. Therefore we used a combination of approaches to understand the potential influence of different variables on the clumped isotope (and oxygen isotope) composition of minerals.We conducted witherite precipitation experiments at a single temperature and at varied pH to empirically determine 13C-18O bond ordering (Δ47) and δ18O of CO32- and HCO3- molecules at a 25 °C equilibrium. Ab initio cluster models based on density functional theory were used to predict equilibrium 13C-18O bond abundances and δ18O of different DIC species and minerals as a function of temperature. Experiments and theory indicate Δ47 and δ18O compositions of CO32- and HCO3- ions are significantly different from each other. Experiments constrain the Δ47-δ18O slope for a pH effect (0.011 ± 0.001; 12 ⩾ pH ⩾ 7). Rapidly-growing temperate corals exhibit disequilibrium mineral isotopic signatures with a Δ47-δ18O slope of 0.011 ± 0.003, consistent with a pH effect.Our theoretical calculations for carbonate minerals indicate equilibrium lattice calcite values for Δ47 and δ18O are intermediate between HCO3− and CO32−. We analyzed synthetic calcites grown at temperatures ranging from 0.5 to 50 °C with and without the enzyme carbonic anhydrase present. This enzyme catalyzes oxygen isotopic exchange between DIC species and is present in many

Validating analysis methodologies used in burnup credit criticality calculations

International Nuclear Information System (INIS)

Brady, M.C.; Napolitano, D.G.

1992-01-01

The concept of allowing reactivity credit for the depleted (or burned) state of pressurized water reactor fuel in the licensing of spent fuel facilities introduces a new challenge to members of the nuclear criticality community. The primary difference in this analysis approach is the technical ability to calculate spent fuel compositions (or inventories) and to predict their effect on the system multiplication factor. Isotopic prediction codes are used routinely for in-core physics calculations and the prediction of radiation source terms for both thermal and shielding analyses, but represent an innovation for criticality specialists. This paper discusses two methodologies currently being developed to specifically evaluate isotopic composition and reactivity for the burnup credit concept. A comprehensive approach to benchmarking and validating the methods is also presented. This approach involves the analysis of commercial reactor critical data, fuel storage critical experiments, chemical assay isotopic data, and numerical benchmark calculations

Excitation functions and isotopic effects in (n, p) reactions for stable nickel isotopes from reaction threshold to 20 MeV

Energy Technology Data Exchange (ETDEWEB)

Lalremruata, B. [Department of Physics, University of Pune, Ganeshkhind, Pune-411007, Maharashtra (India)], E-mail: marema@physics.unipune.ernet.in; Ganesan, S. [Reactor Physics Design Division, BARC, Mumbai 58 (India); Bhoraskar, V.N. [Department of Physics, University of Pune, Ganeshkhind, Pune-411007, Maharashtra (India)], E-mail: vnb@physics.unipune.ernet; Dhole, S.D. [Department of Physics, University of Pune, Ganeshkhind, Pune-411007, Maharashtra (India)], E-mail: sanjay@physics.unipune.ernet.in

2009-05-01

The excitation function for (n, p) reactions from reaction threshold to 20 MeV on five nickel isotopes viz; {sup 58}Ni, {sup 60}Ni, {sup 61}Ni, {sup 62}Ni and {sup 64}Ni were calculated using Talys-1.0 nuclear model code involving the fixed set of global parameters. A good agreement between the calculated and measured data is obtained with minimum effort on parameter fitting and only one free parameter called 'Shell damping factor'. This is of importance to the validation of nuclear model approaches with increased predictive power. The systematic decrease in (n, p) cross-sections with increasing neutron number in reactions induced by neutrons on isotopes of nickel is explained in terms of the proton separation energy and the pre-equilibrium model. The compound nucleus and pre-equilibrium reaction mechanism as well as the isotopic effects were also studied.

Fractionation of carbon isotopes by thermophilic methanogenic bacteria

International Nuclear Information System (INIS)

Ivanov, M.V.; Belyaev, S.S.; Zyakun, A.M.; Bondar, V.A.; Shipin, O.P.; Laurinavichus, K.S.

1985-01-01

The authors investigated the pattern of fractionation of stable carbon isotopes by the thermophilic methane-forming bacteria under different growth conditions and at various rates of formation of methane. A pure culture of Methanobacterium thermoautotrophicum was used in the experiments under the following growth conditions: temperature 65-70 0 C; pH 7.2-7.6; NaCl content 0-0.9 g/liter. The methanogenic bacteria were cultivated in 0.15 liter flasks in mineral medium. A mixture of CO 2 and H 2 in a 1:4 ratio by volume served as the sole carbon and energy source. In all experiments, not more than 5% of the initial CO 2 level was utilized. The rate of methane generation was altered by adjusting the physicochemical growth parameters (temperature from 45-70 0 C, salinity from 0.9 to 40 g/liter NaCl, pH from 6.3 to 7.2). Methane in the samples was quantitatively determined in a chromatograph which had a flame-ionization detector and a column containing Porapak Q sorbent at T = 120 0 C. The carrier gas was CO 2 . The average specific rate of methane formation was calculated as ml CH 4 per mg dry biomass of bacteria per h. Soluble mineral carbon was isolated form the acidified culture liquid in the form of CO 2 and was quantitatively determined in a Chrom-4 chromatography provided with a katharometer and a column containing activated charcoal at T = 150 0 . The gas carrier was helium. The isotopic composition of carbon was determined in a CH-7 mass-spectrometer and was expressed in 13 C values (per thousand) with respect to the international PDB standard

Inferring coastal processes from regional-scale mapping of {sup 222}Radon and salinity: examples from the Great Barrier Reef, Australia

Energy Technology Data Exchange (ETDEWEB)

Stieglitz, Thomas C., E-mail: thomas.stieglitz@jcu.edu.a [AIMS-JCU, Townsville (Australia); Australian Institute of Marine Science, PMB NO 3, Townsville QLD 4810 (Australia); School of Engineering and Physical Sciences, James Cook University, Townsville QLD 4811 (Australia); Cook, Peter G., E-mail: peter.g.cook@csiro.a [CSIRO Land and Water, Private Bag 2, Glen Osmond SA 5064 (Australia); Burnett, William C., E-mail: wburnett@mailer.fsu.ed [Department of Oceanography, Florida State University, Tallahassee, FL 32306 (United States)

2010-07-15

The radon isotope {sup 222}Rn and salinity in coastal surface water were mapped on regional scales, to improve the understanding of coastal processes and their spatial variability. Radon was measured with a surface-towed, continuously recording multi-detector setup on a moving vessel. Numerous processes and locations of land-ocean interaction along the Central Great Barrier Reef coastline were identified and interpreted based on the data collected. These included riverine fluxes, terrestrially-derived fresh submarine groundwater discharge (SGD) and the tidal pumping of seawater through mangrove forests. Based on variations in the relationship of the tracers radon and salinity, some aspects of regional freshwater inputs to the coastal zone and to estuaries could be assessed. Concurrent mapping of radon and salinity allowed an efficient qualitative assessment of land-ocean interaction on various spatial and temporal scales, indicating that such surveys on coastal scales can be a useful tool to obtain an overview of SGD locations and processes.

Calcium isotope fractionation between aqueous compounds relevant to low-temperature geochemistry, biology and medicine

Science.gov (United States)

Moynier, Frédéric; Fujii, Toshiyuki

2017-03-01

Stable Ca isotopes are fractionated between bones, urine and blood of animals and between soils, roots and leaves of plants by >1000 ppm for the 44Ca/40Ca ratio. These isotopic variations have important implications to understand Ca transport and fluxes in living organisms; however, the mechanisms of isotopic fractionation are unclear. Here we present ab initio calculations for the isotopic fractionation between various aqueous species of Ca and show that this fractionation can be up to 3000 ppm. We show that the Ca isotopic fractionation between soil solutions and plant roots can be explained by the difference of isotopic fractionation between the different first shell hydration degree of Ca2+ and that the isotopic fractionation between roots and leaves is controlled by the precipitation of Ca-oxalates. The isotopic fractionation between blood and urine is due to the complexation of heavy Ca with citrate and oxalates in urine. Calculations are presented for additional Ca species that may be useful to interpret future Ca isotopic measurements.

Calculations of kinetic isotope effects in the Hofmann eliminations of substituted (2-phenylethyl)trimethylammonium ions

International Nuclear Information System (INIS)

Lewis, D.E.; Sims, L.B.; Yamataka, H.; McKenna, J.

1980-01-01

Theoretical calculations of kinetic isotope effects (KIE) for the Hofmann elimination of the (2-phenylethyl)trimethylammonium ion (I,Z = H) have been carried out for an extensive series of transition-state models encompassing the Elcb-like region of the E2 mechanistic spectrum. The reaction coordinate employed corresponded to the irreversible fragmentation of the base-H'-C/sub β/-C/sub α/-N system, with proton transfer being the dominant contributor. Structural parameters (bond distances and angles) were related to the independent bond orders n/sub α-N/ and n/sub β-H'/ by empirical and semiempirical relationships. The most probable transition-state structure for the reaction was determined by interpolation of the experimental values for the β-D 2 and 15 N KIE into plots of the trends of the calculated KIE. The nonsolvated models obtained in this manner gave only poor agreement between calculated and experimental secondary deuterium (α-D 2 ) and leaving group deuterium [N(CD 3 )/sub x/(CH 3 )/sub 3-x/, x = 1 to 3) KIE; explicit consideration of differential solvation of the reactant and transition state afforded the most chemically reasonable resolution of these discrepancies. Using solvated models, transition-state structures were also determined for the Hofmann elimination of parasubstituted derivatives of I (Z = OCH 3 , Cl, CF 3 ). These transition states are related by a shift parallel to the central E2 diagogonal of an O'Ferrall-Jencks reaction diagram, as predicted by Thorton, indicating that, in the absence of other factors (differing solvent or base, etc.), the extent to which negative charge is accumulated at Cβ in the transition state is solely a factor of the leaving group. Both independent bond orders (n/sub α-N/ and n/sub β-H'/) exhibit a linear dependence on the sigma value of the substituent, allowing for the first time prediction of transition states

Method for measurement of flowing water salinity within or behind wellbore casing

International Nuclear Information System (INIS)

Arnold, D.M.

1986-01-01

Water flowing within or behind a wellbore casing is irradiated with 14 MeV neutrons from a source in a downhole sonde. Gamma radiation from the isotope nitrogen-16 induced from the O 16 (n,p)N 16 reaction and the products of either the Na 23 (n,α)F 20 or the Cl 37 (n,α)p 34 reactions is measured in intensity and energy with detectors in the sonde. From the gamma radiation measurements, the relative presence of oxygen to at least one of sodium or chlorine in the water is measured, and from the measurement the salinity of the water is determined

Collinear resonance ionization spectroscopy of exotic francium and radium isotopes

CERN Document Server

AUTHOR|(CDS)2094150

Two experimental campaigns were performed at the Collinear Resonance Ionization Spectroscopy (CRIS) experiment, located at the ISOLDE radioactive-beam facility. The spectroscopic quadrupole moment of $^{203}$Fr was measured. Its magnitude with respect to the other even-$N$ francium isotopes below $N = 126$ suggests an onset of static deformation. However, calculations of the static and total deformation parameters reveal that it cannot be considered as purely statically deformed. The neutron-rich radium isotopes were investigated. The spectroscopic quadrupole moment of $^{231}$Ra was measured and the continuation of increasing quadrupole deformation with neutron number in neutron-rich radium isotopes was further established. Measurements of the changes in mean-square charge radii of $^{231,233}$Ra allowed the odd-even staggering parameter to be calculated for $^{230-232}$Ra. A normal odd-even staggering which increases in magnitude with neutron number was observed in these isotopes.

Guideline on Isotope Dilution Mass Spectrometry

Energy Technology Data Exchange (ETDEWEB)

Gaffney, Amy [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

2017-05-19

Isotope dilution mass spectrometry is used to determine the concentration of an element of interest in a bulk sample. It is a destructive analysis technique that is applicable to a wide range of analytes and bulk sample types. With this method, a known amount of a rare isotope, or ‘spike’, of the element of interest is added to a known amount of sample. The element of interest is chemically purified from the bulk sample, the isotope ratio of the spiked sample is measured by mass spectrometry, and the concentration of the element of interest is calculated from this result. This method is widely used, although a mass spectrometer required for this analysis may be fairly expensive.

Modeling daily soil salinity dynamics in response to agricultural and environmental changes in coastal Bangladesh

Science.gov (United States)

Payo, Andrés.; Lázár, Attila N.; Clarke, Derek; Nicholls, Robert J.; Bricheno, Lucy; Mashfiqus, Salehin; Haque, Anisul

2017-05-01

Understanding the dynamics of salt movement in the soil is a prerequisite for devising appropriate management strategies for land productivity of coastal regions, especially low-lying delta regions, which support many millions of farmers around the world. At present, there are no numerical models able to resolve soil salinity at regional scale and at daily time steps. In this research, we develop a novel holistic approach to simulate soil salinization comprising an emulator-based soil salt and water balance calculated at daily time steps. The method is demonstrated for the agriculture areas of coastal Bangladesh (˜20,000 km2). This shows that we can reproduce the dynamics of soil salinity under multiple land uses, including rice crops, combined shrimp and rice farming, as well as non-rice crops. The model also reproduced well the observed spatial soil salinity for the year 2009. Using this approach, we have projected the soil salinity for three different climate ensembles, including relative sea-level rise for the year 2050. Projected soil salinity changes are significantly smaller than other reported projections. The results suggest that inter-season weather variability is a key driver of salinization of agriculture soils at coastal Bangladesh.

Effect of Different Alternate Irrigation Strategies using Saline and Non-Saline Water on Corn Yield, Salinity and Moisture Distribution in Soil Profile

Directory of Open Access Journals (Sweden)

Ali Reza Kiani

2017-01-01

Full Text Available Introduction: Lack of water and deterioration in the quality of soil and water resources are considered to be the prime cause of reduced crop yield in arid and semi-arid regions ‘More crop per drop’ by trickle irrigation, deficit irrigation, and uncommon water are the best strategies for mitigating water crises. Different irrigation management strategies are needed to increase production in different areas. In areas where sufficient water is available, a full irrigation strategy could be a suitable option, while in areas where water is limited, deficit irrigation would be an appropriate method, and finally in areas where water resources are saline, management strategies for achieving sustainable production as well as economic yields would be suitable. Maize is the third most important grain crop in the world following wheat and rice and it is the main source of nutrition for humans and animals. Because of the importance of maize in the world, increasing maize production under environmental stresses is a big challenge for agricultural scientists. Different methods of irrigation and the use of saline water that had satisfactory results for increasing agricultural production have been studied by several investigators . The main objective of this study was to establish an efficient use of limited water resources as well as to explore the possibility of replacing saline water with fresh water using different management techniques. Materials and Methods: A field experiment was conducted over two maize cropping seasons (2012–2013 in northern Iran (Gorgan Agricultural Research Station to compare different alternate irrigation scenarios using saline water on corn yield, salinity and soil moisture distribution in a randomized complete block design with three replications. Treatments were: T1 and T2 = 100 and 50 % of crop water requirement with non-saline water, respectively; T3 and T4 = variable and fixed full irrigation with saline and non-saline

Isotope effect on the zero point energy shift upon condensation

International Nuclear Information System (INIS)

Kornblum, Z.C.; Ishida, T.

1977-07-01

The various isotope-dependent and independent atomic and molecular properties that pertain to the isotopic difference between the zero point energy (ZPE) shifts upon condensation were derived. The theoretical development of the change of the ZPE associated with the internal molecular vibrations, due to the condensation of the gaseous molecules, is presented on the basis of Wolfsberg's second-order perturbation treatment of the isotope-dependent London dispersion forces between liquid molecules. The isotope effect on the ZPE shift is related to the difference between the sums of the integrated intensities of the infrared absorption bands of the two gaseous isotopic molecules. The effective atomic charges are also calculated from available experimental infrared intensity data. The effects of isotopic substitutions of carbon-13 for carbon-12 and/or deuterium for protium, in ethylene, methane, and the fluorinated methanes, CH 3 F, CH 2 F 2 , CHF 3 , and CF 4 , on the ZPE shift upon condensation are calculated. These results compare well with the Bigeleisen B-factors, which are experimentally obtained from vapor pressure measurements of the isotopic species. Each of the following molecular properties will tend to increase the isotopic difference between the ZPE shifts upon condensation: (1) large number of highly polar bonds, (2) high molecular weight, (3) non-polar (preferably) or massive molecule, (4) non-hydrogenous molecule, and (5) closely packed liquid molecules. These properties will result in stronger dispersion forces in the liquid phase between the lighter molecules than between the isotopically heavier molecules. 36 tables, 9 figures

Computational study of substrate isotope effect probes of transition state structure for acetylcholinesterase catalysis

International Nuclear Information System (INIS)

Sikorski, R.S.; Malany, S.; Seravalli, J.; Quinn, D.M.

2002-01-01

Secondary isotope effects for carbonyl addition reactions of methyl thioacetate, acetone and acetaldehyde have been calculated by ab initio quantum mechanical methods in an effect to interpret measured β-deuterium isotope effects on acetylcholinesterase-catalysed hydrolysis of acetylthiocholine. The calculated β-deuterium isotope effect for equilibrium addition of methanol to methyl thioacetate is D3 K eq = 0.965, and the corresponding effect for addition of methoxide ion to methyl thioacetate wherein three waters are hydrogen bonded to the carbonyl oxyanion is D3 K eq = 1.086. Neither of these calculated isotope effects is an inverse as the experimental β-deuterium isotope effect for acetylcholinesterase-catalysed hydrolysis of acetylthiocholine, D3 K eq = 0.90±0.03. Structural comparisons show that the water-solvated methoxide adduct of methyl thioacetate is more expanded than is the natural methanol addition adduct, and suggest that the degree of which the isotope effect is inverse (i.e. less than) is inversely correlated to the degree of expansion of the adduct. A similar correlation of α-deuterium and β-deuterium secondary isotope effects with the degree of expansion of the adducts is found for equilibrium additions of methanol and methoxide ion to acetylaldehyde. These computational results suggest that the markedly inverse β-deuterium isotope effect for the acetylcholinesterase reaction arises from enzymatic compression of the transition state. (author)

Core excitations to the low lying states of thallium isotopes

International Nuclear Information System (INIS)

Gruenbaum, L.; Tomaselli, M.; Herold, D.

1977-08-01

The admixture of core excitations to the low lying states of A = 203 and A = 205 thallium isotopes has been calculated. The wave functions obtained reproduce the electromagnetic properties as well as the hyperfine splittings and the isomershifts of both thallium isotopes. (orig.) [de

Pressure–Temperature–Fluid Constraints for the Poona Emerald Deposits, Western Australia: Fluid Inclusion and Stable Isotope Studies

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Dan Marshall

2016-12-01

Full Text Available Emerald from the deposits at Poona shows micrometre-scale chemical, optical, and cathodoluminescence zonation. This zonation, combined with fluid inclusion and isotope studies, indicates early emerald precipitation from a single-phase saline fluid of approximately 12 weight percent NaCl equivalent, over the temperature range of 335–525 °C and pressures ranging from 70 to 400 MPa. The large range in pressure and temperature likely reflects some post entrapment changes and re-equilibration of oxygen isotopes. Secondary emerald-hosted fluid inclusions indicate subsequent emerald precipitation from higher salinity fluids. Likewise, the δ18O-δD of channel fluids extracted from Poona emerald is consistent with multiple origins yielding both igneous and metamorphic signatures. The combined multiple generations of emerald precipitation, different fluid compositions, and the presence of both metamorphic and igneous fluids trapped in emerald, likely indicate a protracted history of emerald precipitation at Poona conforming to both an igneous and a metamorphic origin at various times during regional lower amphibolite to greenschist facies metamorphism over the period ~2710–2660 Ma.

Studying Vegetation Salinity: From the Field View to a Satellite-Based Perspective

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Rachel Lugassi

2017-02-01

Full Text Available Salinization of irrigated lands in the semi-arid Jezreel Valley, Northern Israel results in soil-structure deterioration and crop damage. We formulated a generic rule for estimating salinity of different vegetation types by studying the relationship between Cl/Na and different spectral slopes in the visible–near infrared–shortwave infrared (VIS–NIR–SWIR spectral range using both field measurements and satellite imagery (Sentinel-2. For the field study, the slope-based model was integrated with conventional partial least squares (PLS analyses. Differences in 14 spectral ranges, indicating changes in salinity levels, were identified across the VIS–NIR–SWIR region (350–2500 nm. Next, two different models were run using PLS regression: (i using spectral slope data across these ranges; and (ii using preprocessed spectral reflectance. The best model for predicting Cl content was based on continuum removal reflectance (R2 = 0.84. Satisfactory correlations were obtained using the slope-based PLS model (R2 = 0.77 for Cl and R2 = 0.63 for Na. Thus, salinity contents in fresh plants could be estimated, despite masking of some spectral regions by water absorbance. Finally, we estimated the most sensitive spectral channels for monitoring vegetation salinity from a satellite perspective. We evaluated the recently available Sentinel-2 imagery’s ability to distinguish variability in vegetation salinity levels. The best estimate of a Sentinel-2-based vegetation salinity index was generated based on a ratio between calculated slopes: the 490–665 nm and 705–1610 nm. This index was denoted as the Sentinel-2-based vegetation salinity index (SVSI (band 4 − band 2/(band 5 + band 11.

Hydrogeochemistry and Stable Isotope Studies of Groundwater in the Ga West Municipal Area, Ghana

International Nuclear Information System (INIS)

Saka, David

2011-07-01

This study assesses groundwater in the Ga West Municipal Area of Ghana using hydrogeochemistry and stable isotope approaches. High salinity groundwaters are obtained in the municipality which poses problems for current and future domestic water supply exploitation. The increase in salinity is related to the dissolution of minerals in the host rocks and the evaporative concentration of solutes. The dominant groundwater composition in both shallow and deep wells sampled is Na-Cl, with concentration increasing substantially with well depths. The mixing process between freshwater and saline water was observed in the shift from CaHCO3 facies to Ca-Cl facies. Schoeller diagrams showed that groundwater movement in the study area is mostly vertical, moving from the shallow groundwaters towards the deep groundwaters. There were however few exceptions where no relationship was established between the shallow and the deep groundwaters. The oxygen and hydrogen isotope compositions in the groundwater samples suggest that groundwater recharge is of meteoric origin, with few samples showing evidence of evaporation. An average deuterium excess of rainfall of 14.2‰ was observed, which indicates the significance of kinetic evaporation due to low humidity conditions prevalent in the study area. The d-excess also indicates modern recharge along the Akwapim-Togo Ranges. Groundwater analysis for trace metals indicates that 93% of the groundwaters have Iron concentration above recommended limits. However, Cu, Zn, Pb, Cd and Cr have values within the acceptable limits. Generally, about 40% of the groundwaters sampled are not suitable for drinking and domestic purposes based on comparison with international standards for drinking water. (au)

Characteristics of isotope-selective chemical reactor with gas-separating device

International Nuclear Information System (INIS)

Gorshunov, N.M.; Kalitin, S.A.; Laguntsov, N.I.; Neshchimenko, Yu.P.; Sulaberidze, G.A.

1988-01-01

A study was made on characteristics of separating stage, composed of isotope-selective chemical (or photochemical) reactor and membrane separating cascade (MSC), designated for separation of isotope-enriched products from lean reagents. MSC represents the counterflow cascade for separation of two-component mixtures. Calculations show that for the process of carton isotope separation the electric power expences for MSC operation are equal to 20 kWxh/g of CO 2 final product at 13 C isotope content in it equal to 75%. Application of the membrane gas-separating cascade at rather small electric power expenses enables to perform cascading of isotope separation in the course of nonequilibrium chemical reactions

Multiple-isotope separation in gas centrifuge

International Nuclear Information System (INIS)

Wood, Houston G.; Mason, T.C.; Soubbaramayer

1996-01-01

In previous works, the Onsager's pancake equation was used to provide solution to the internal counter-current flow field, which is necessary to calculate solutions to the isotope transport equation. The diffusion coefficient was assumed to be constant which is a good approximation for gases with large molecular weights, and small differences in the molecular weights of the various isotopes. A new optimization strategy was presented for determining the operating parameters of a gas centrifuge to be used for multiple-component isotope separation. Scoop drag, linear wall temperature gradient, the feed rate ant the cut have been chosen as operating parameters for the optimization. The investigation was restricted to a single centrifuge, and the problem of cascading for multiple-isotope separation was not addressed. The model describing the flow and separation phenomena in centrifuge includes a set of equations describing the fluid dynamics of the counter-current flow and the diffusion equations written for each isotope of the mixture. In this paper, an optimization algorithm is described and applied to an example for the re enrichment of spent reactor uranium

Theoretical calculation of cryogenic distillation for two-component hydrogen isotope system

International Nuclear Information System (INIS)

Xia Xiulong; Luo Yangming; Wang Heyi; Fu Zhonghua; Liu Jun; Han Jun; Gu Mei

2005-10-01

Cryogenic distillation model for single column was built to simulating hydrogen isotope separation system. Three two-component system H 2 /HD, H 2 /HT and D 2 /DT was studied. Both temperature and concentration distribution was obtained and the results show a clear separation characteristics. H 2 /HT has the best separation performance while D 2 /DT was the most difficult to separate. (authors)

Hydrochemical Characteristics and Formation of the Saline or Salty Springs in Eastern Sichuan Basin of China

Science.gov (United States)

Zhou, X.

2017-12-01

Saline or salty springs provide important information on the hydrogeochemical processes and hydrology within subsurface aquifers. More than 20 saline and salty springs occur in the core of anticlines in the eastern Sichuan Basin in southwestern China where the Lower and Middle Triassic carbonates outcrop. Water samples of 8 saline and salty springs (including one saline hot spring) were collected for analyses of the major and minor constituents, trace elements and stable oxygen and hydrogen isotopes. The TDS of the springs range from 4 to 83 g/L, and they are mainly of Cl-Na type. Sr, Ba and Li are the predominant trace elements. The δ2H and δ18O of the water samples indicate that they are of meteoric origin. The source of salinity of the springs originates from dissolution of minerals in the carbonates, including halite, gypsum, calcite and dolomite. The formation mechanism of the springs is that groundwater receives recharge from infiltration of precipitation, undergoes shallow or deep circulation in the core of the anticline and incongruent dissolution of the salt-bearing carbonates occurs, and emerges in the river valley in the form of springs with relatively high TDS. The 8 springs can be classified into 4 springs of shallow groundwater circulation and 4 springs of deep groundwater circulation according to the depth of groundwater circulation, 7 springs of normal temperature and 1 hot spring according to temperature. There are also 2 up-flow springs: the carbonate aquifers are overlain by relatively impervious sandstone and shale, groundwater may flows up to the ground surface through the local portion of the overlying aquiclude where fractures were relatively well developed, and emerges as an up-flow spring. Knowledge of the hydrochemical characteristics and the geneses of the saline and salty springs are of important significance for the utilization and preservation of the springs.

Synopsis of strontium isotope variations in groundwater at Aspo, southern Sweden

Science.gov (United States)

Peterman, Z.E.; Wallin, B.

1999-01-01

Strontium isotope ratios are used to identify end-member ground-water compositions at Aspo in southeastern Sweden where the Hard Rock Laboratory (HRL) has been constructed to evaluate the suitability of crystalline rock for the geologic disposal of nuclear waste. The Hard Rock Laboratory is a decline (tunnel) constructed in 1.8 Ga-old granitic rock that forms islands in an archipelago along the Swedish coast. Ground-water samples were obtained for isotopic analyses from boreholes drilled from the surface and from side boreholes drilled within the HRL. Infiltration at Aspo occurs primarily through fractures zones in the granitic bedrock beneath thin soils throughout the area. Because of extremely low Sr concentrations, rain and snow are not important contributors to the Sr isotope budget of the ground-water system. At shallow levels, water percolating downward along fractures and fracture zones acquires a ??87Sr between +9.5 and +10.0??? and maintains this value downward while Sr concentrations increase by two orders of magnitude. Ground-water samples from both boreholes and from in the HRL show the effects of mixing with saline waters containing as much as 59 mg/L Sr and ??87Sr values as large as +13.92%, Baltic Sea water is a potential component of the groundwater system with ??87Sr values only slightly larger than modern marine values (+0.3???) but with much lower concentrations (1.5 mg/L) than ocean water (8 mg/L). However, because of large Sr concentration differences between the saline groundwater (59 mg/L) and Baltic Sea water (1.5 rag/L), ??87Sr values are not particularly sensitive indicators of sea-water intrusion even though their ??87Sr values differ substantially.

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

International Nuclear Information System (INIS)

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

1999-01-01

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

Application of environmental isotopes to groundwater investigations in Qatar

International Nuclear Information System (INIS)

Yurtsever, Y.; Payne, B.R.

1978-01-01

Environmental isotope techniques have been used to study the dynamic behaviour of the groundwater systems in Qatar. The aim was to identify the mixing processes between the shallow phreatic aquifer, the deep confined aquifers and seawater. Environmental tritium was used to estimate the average recharge of the shallow freshwater aquifer. The results of the environmental isotope study, supplemented by hydrochemical data, have clearly indicated that in the south western part of the peninsula the shallow aquifer is in direct hydraulic connection with the deeper artesian aquifers. Furthermore, the poor quality of water in that area is mainly due to substantial upward leakage of water from the deeper aquifers. In some parts of the peninsula seawater was identified as an additional source of salinity. A model was developed for estimating the turnover rate and average recharge of the phreatic aquifer from the tritium data. The results of this model provide an independent estimate of the average annual recharge. (orig.) [de

Application of environmental isotopes to groundwater investigations in Qatar

International Nuclear Information System (INIS)

Yurtsever, Y.; Payne, B.R.

1979-01-01

Environmental isotope techniques have been used to study the dynamic behaviour of the groundwater systems in Qatar. The aim was to identify the mixing processes between the shallow phreatic aquifer, the deep confined aquifers and sea-water. Environmental tritium was used to estimate the average recharge of the shallow fresh-water aquifer. The results of the environmental isotope study, supplemented by hydrochemical data, have clearly indicated that in the southwestern part of the peninsula the shallow aquifer is in direct hydraulic connection with the deeper artesian aquifers. Furthermore, the poor quality of water in that area is mainly due to substantial upward leakage of water from the deeper aquifers. In some parts of the peninsula sea-water was identified as an additional source of salinity. A model was developed for estimating the turnover rate and average recharge of the phreatic aquifer from the tritium data. The results of this model provide an independent estimate of the average annual recharge. (author)

Determination of uranium, thorium and radium isotope ratio

International Nuclear Information System (INIS)

Sokolova, Z.A.

1983-01-01

The problems connected with the study of isotope composition of natural radioactive elements in natural objects are considered. It is pointed out that for minerals, ores and rocks the following ratios are usually determined: 234 U/ 238 U, 230 Th/ 238 U, 226 Ra/ 238 U, 228 Th/ 230 Th, 228 Th/ 232 Th and lead isotopes; for natural waters, besides the enumerated - 226 Ra/ 228 Ra. General content of uranium and thorium in the course of isotope investigations is determined from separate samples, most frequently by the X-ray spectral method, radium content - by usual radiochemical method, uranium and radium content in waters -respectively by calorimetric and emanation methods. Radiochemical preparation of geologic powder and aqueous samples for isotope analysis is described in detail. The technique of measuring and calculating isotope ratios (α-spectrometry for determining isotope composition of uranium and thorium and emanation method for determining 226 Ra/ 228 Ra) is presented

Evidence for Upward Flow of Saline Water from Depth into the Mississippi River Valley Alluvial Aquifer in Southeastern Arkansas

Science.gov (United States)

Larsen, D.; Paul, J.

2017-12-01

Groundwater salinization is occurring in the Mississippi River Valley Alluvial (MRVA) aquifer in southeastern Arkansas (SE AR). Water samples from the MRVA aquifer in Chicot and Desha counties have yielded elevated Cl-concentrations with some as high as 1,639 mg/L. Considering that the MRVA aquifer is the principle source of irrigation water for the agricultural economy of SE AR, salinization needs to be addressed to ensure the sustainability of crop, groundwater, and soil resources in the area. The origin of elevated salinity in MRVA aquifer was investigated using spatial and factor analysis of historical water quality data, and sampling and tracer analysis of groundwater from irrigation, municipal, and flowing industrial wells in SE AR. Spatial analysis of Cl- data in relation to soil type, geomorphic features and sand-blow density indicate that the Cl- anomalies are more closely related to the sand-blow density than soil data, suggesting an underlying tectonic control for the distribution of salinity. Factor analysis of historical geochemical data from the MRVA and underlying Sparta aquifer shows dilute and saline groups, with saline groups weighted positively with Cl- or Na+ and Cl-. Tracer data suggest a component of evaporatively evolved crustal water of pre-modern age has mixed with younger, fresher meteoric sources in SE AR to create the saline conditions in the MRVA aquifer. Stable hydrogen and oxygen values of waters sampled from the Tertiary Sparta and MRVA aquifers deviate from the global and local meteoric water lines along an evaporative trend (slope=4.4) and mixing line with Eocene Wilcox Group groundwaters. Ca2+ and Cl- contents vary with Br- along mixing trends between dilute MRVA water and Jurassic Smackover Formation pore fluids in southern AR. Increasing Cl- content with C-14 age in MRVA aquifer groundwater suggests that the older waters are more saline. Helium isotope ratios decrease with He gas content for more saline water, consistent with

Simulated Effects of Soil Temperature and Salinity on Capacitance Sensor Measurements

Directory of Open Access Journals (Sweden)

Timothy R. Green

2007-04-01

Full Text Available Dielectric measurement techniques are used widely for estimation of water contentin environmental media. However, factors such as temperature and salinity affecting thereadings require further quantitative investigation and explanation. Theoretical sensitivities ofcapacitance sensors to liquid salinity and temperature of porous media were derived andcomputed using a revised electrical circuit analogue model in conjunction with a dielectricmixing model and a finite element model of Maxwell’s equation to compute electrical fielddistributions. The mixing model estimates the bulk effective complex permittivities of solid-water-air media. The real part of the permittivity values were used in electric field simulations,from which different components of capacitance were calculated via numerical integration forinput to the electrical circuit analogue. Circuit resistances representing the dielectric losses werecalculated from the complex permittivity of the bulk soil and from the modeled fields. Resonantfrequencies from the circuit analogue were used to update frequency-dependent variables in aniterative manner. Simulated resonant frequencies of the capacitance sensor display sensitivitiesto both temperature and salinity. The gradients in normalized frequency with temperatureranged from negative to positive values as salinity increased from 0 to 10 g L-1. The modeldevelopment and analyses improved our understanding of processes affecting the temperatureand salinity sensitivities of capacitance sensors in general. This study provides a foundation forfurther work on inference of soil water content under field conditions.

Statistical Classification Of the Environmental Isotopes and the Hydrochemical data in the main Shallow Coastal Aquifer System in North West, Egypt

International Nuclear Information System (INIS)

Nada, A.A.; AL-Gamal, S.A.

1999-01-01

Multivariate statistical analysis of hydrochemical data and environmental isotopes were used in differentiating ground waters of different types within the quaternary aquifer in the north western coast of Egypt. Three main groups of water types were differentiated, in close agreement with three isotopic water groups, based on field and laboratory studies. The first group includes the sodium bicarbonate water type of meteoric origin (cluster 1 in multivariate analysis and isotopic water group 1) whereas, the second group includes both sodium chloride and sodium sulphate waters.(cluster in multivariate analysis and isotopic group 2). The third group represents ground water of salt water intrusion whose water type is sodium chloride (cluster 111 and isotopic water groups 3) .The data show that salinity ranges from 385 mg/L representing very fresh water to 12260 mg/L representing water contaminated with marine water due to excessive pumping in some Localities.

Finding a solution: Heparinised saline versus normal saline in the maintenance of invasive arterial lines in intensive care.

Science.gov (United States)

Everson, Matthew; Webber, Lucy; Penfold, Chris; Shah, Sanjoy; Freshwater-Turner, Dan

2016-11-01

We assessed the impact of heparinised saline versus 0.9% normal saline on arterial line patency. Maintaining the patency of arterial lines is essential for obtaining accurate physiological measurements, enabling blood sampling and minimising line replacement. Use of heparinised saline is associated with risks such as thrombocytopenia, haemorrhage and mis-selection. Historical studies draw variable conclusions but suggest that normal saline is at least as effective at maintaining line patency, although recent evidence has questioned this. We conducted a prospective analysis of the use of heparinised saline versus normal saline on unselected patients in the intensive care of our hospital. Data concerning duration of 471 lines insertion and reason for removal was collected. We found a higher risk of blockage for lines flushed with normal saline compared with heparinised saline (RR = 2.15, 95% CI 1.392-3.32, p  ≤ 0.001). Of the 56 lines which blocked initially (19 heparinised saline and 37 normal saline lines), 16 were replaced with new lines; 5 heparinised saline lines and 11 normal saline lines were reinserted; 5 of these lines subsequently blocked again, 3 of which were flushed with normal saline. Our study demonstrates a clinically important reduction in arterial line longevity due to blockages when flushed with normal saline compared to heparinised saline. We have determined that these excess blockages have a significant clinical impact with further lines being inserted after blockage, resulting in increased risks to patients, wasted time and cost of resources. Our findings suggest that the current UK guidance favouring normal saline flushes should be reviewed.

Preliminary isotopic study of Lake Asal system (Republic of Djibouti)

International Nuclear Information System (INIS)

Fontes, J.C.; Zuppi, G.M.; Florkowski, T.; Pouchan, P.

1979-01-01

The saline Lake Asal at 155 m below sea level in the Afar Rift (Republic of Djibouti) is fed mainly by sea water. In spite of the intense evaporation (about 3 m annually), the 18 O and deuterium enrichments of the lake water are relatively low, because of the reduced activity of water as a consequence of the high salt content. Isotopic balance of the lake, as well as lithium and sulphate balances, support the hypothesis of leakages from the lake of about 15 to 20% of the inflow. (author)

Assessment of Bacterial Degradation of Aromatic Hydrocarbons in the Environment by Analysis of Stable Carbon Isotope Fractionation

International Nuclear Information System (INIS)

Meckenstock, Rainer U.; Morasch, Barbara; Kaestner, Matthias; Vieth, Andrea; Richnow, Hans Hermann

2002-01-01

13 C/ 12 C stable carbon isotope fractionation was used to assess biodegradation in contaminated aquifers with toluene as a model compound. Different strains of anaerobic bacteria (Thauera aromatica, Geobacter metallireducens, and the sulfate-reducing strain TRM1) showed consistent 13 C/ 12 C carbon isotope fractionation with fractionation factors between αC = 1.0017 and 1.0018. In contrast, three cultures of aerobic organisms, using different mono- and dioxygenase enzyme systems to initiate toluene degradation, showed variable isotope fractionation factors of αC = 1.0027 (Pseudomonasputida strain mt-2), αC = 1.0011 (Ralstonia picketii), andαC = 1.0004 (Pseudomonas putida strain F1). The great variability of isotope fractionation between different aerobic bacterial strains suggests that interpretation of isotope data in oxic habitats can only be qualitative. A soil column was run as a model system for contaminated aquifers with toluene as the carbon source and sulfate as the electron acceptor and samples were taken at different ports along the column. Microbial toluene degradation was calculated based on the 13 C/ 12 C isotope fractionation factors of the batch culture experiments together with the observed 13 C/ 12 C isotope shifts of the residual toluene fractions. The calculated percentage of biodegradation, B, correlated well with the decreasing toluene concentrations at the sampling ports and indicated the increasing extent of biodegradation along the column. The theoretical toluene concentrations as calculated based on the isotope values matched the measured concentrations at the different sampling ports indicating that the Rayleigh equation can be used to calculate biodegradation in quasi closed systems based on measured isotope shifts. A similar attempt was performed to assess toluene degradation in a contaminated, anoxic aquifer. A transect of groundwater wells was monitored along the main direction of the groundwater flow and revealed decreasing

Investigation of water and saline solution drops evaporation on a solid substrate

Directory of Open Access Journals (Sweden)

Orlova Evgenija G.

2014-01-01

Full Text Available Experimental investigation water and saline solution drops evaporation on a solid substrate made of anodized aluminum is presented in the paper. Parameters characterizing drop profile have been obtained (contact angle, contact diameter, height. The specific evaporation rate has been calculated from obtained values. It was found that water and saline solution drops with concentration up to 9.1% evaporate in the pinning mode. However, with increasing the salt concentration in the solution up to 16.7% spreading mode was observed. Two stages of drop evaporation depending on change of the evaporation rate have been separated.

Further development of IDGS: Isotope dilution gamma-ray spectrometry

International Nuclear Information System (INIS)

Li, T.K.; Parker, J.L.; Kuno, Y.; Sato, S.; Kamata, M.; Akiyama, T.

1991-01-01

The isotope dilution gamma-ray spectrometry (IDGS) technique for determining the plutonium concentration and isotopic composition of highly radioactive spent-fuel dissolver solutions has been further developed. Both the sample preparation and the analysis have been improved. The plutonium isotopic analysis is based on high-resolution, low-energy gamma-ray spectrometry. The plutonium concentration in the dissolver solutions then is calculated from the measured isotopic differences among the spike, the dissolver solution, and the spiked dissolver solution. Plutonium concentrations and isotopic compositions of dissolver solutions analyzed from this study agree well with those obtained by traditional isotope dilution mass spectrometry (IDMS) and are consistent with the first IDGS experimental result. With the current detector efficiency, sample size, and a 100-min count time, the estimated precision is ∼0.5% for 239 Pu and 240 Pu isotopic analyses and ∼1% for the plutonium concentration analysis. 5 refs., 2 figs., 7 tabs

Isotopic alloying to tailor helium production rates in mixed spectrum reactors

International Nuclear Information System (INIS)

Mansur, L.K.; Rowcliffe, A.F.; Grossbeck, M.L.; Stoller, R.E.

1985-01-01

The purposes of this work are to increase the understanding of mechanisms by which helium affects microstructure and properties, to aid in the development of materials for fusion reactors, and to obtain data from fission reactors in regimes of direct interest for fusion reactor applications. Isotopic alloying is examined as a means of manipulating the ratio of helium transmutations to atom displacements in mixed spectrum reactors. The application explored is based on artificially altering the relative abundances of the stable isotopes of nickel to systematically vary the fraction of 58 Ni in nickel bearing alloys. The method of calculating helium production rates is described. Results of example calculations for proposed experiments in the High Flux Isotope Reactor are discussed

The study of multicomponent separation of Xe isotope by centrifugal method

International Nuclear Information System (INIS)

Jinyan Wu; Fu Zhuge

1996-01-01

The element Xe has nine isotopes in nature, the separation performance of each component mutually affects the others, so the binary separation theory can't be employed to study the multicomponent separation. Especially, when the molecular wight of a certain component is in the middle of its isotope components, the effect of the others on this component must be considered. In this paper, first, the multicomponent separation of Xe isotopes in a gas centrifuge is studied, with the consideration of the effect of the concentration on the diffusion coefficient and average molecular weight. The multicomponent diffusion equations are solved by the finite difference method. Second, the enrichment of Xe isotopes in a cascade is studied. On the basis of the study of a gas centrifuge, the simplified separation equations of a gas centrifuge for cascade calculation are obtained. Furthermore, the complete equations of the cascade separation are established according to the conservation of mass of each component and solved by a numerical method. The study of this paper can be extended for other isotope separation calculations. (author)

Sulfur Isotope Exchange between S-35 Labeled Inorganic Sulfur-Compounds in Anoxic Marine-Sediments

DEFF Research Database (Denmark)

FOSSING, H.; THODEANDERSEN, S.; JØRGENSEN, BB

1992-01-01

of isotope exchange, specific radioactivities of the reduced sulfur pools were poorly defined and could not be used to calculate their rates of formation. Such isotope exchange reactions between the reduced inorganic sulfur compounds will affect the stable isotope distribution and are expected to decrease...

Saline agriculture: A technology for economic utilization and improvement of saline environments (abstract)

International Nuclear Information System (INIS)

Aslam, Z.; Malik, K.A.; Khurshid, S.J.; Awan, A.R.; Akram, M.; Hashmi, Z.; Ali, Y.; Gulnaz, A.; Hussain, M.; Hussain, F.

2005-01-01

The salinity problem is one of the severe constraints for agriculture in Pakistan. In a socio-economic and salinity and drainage survey over an area of about 25000 acres of salt-affected land recently, crop production is found to be very low. Livestock is underfed and malnourished. Pakistan has spent and allocated over one billion US dollars on Salinity Control and Reclamation Projects (SCARP), of course, with dubious results. Over the years, a Saline Agriculture Technology has been developed as a cheap alternative at NIAB for comfortably living with salinity and to profitably utilize saline land rather than its reclamation. The soil improvement is a fringe benefit in this approach. The Saline Agriculture Technology has been tested at laboratory level, at field stations and at farms of some progressive farmers. Now we are sharing this technology with farming communities through a 'Saline Agriculture Farmer Participatory Development Project in Pakistan', with assistance from the National Rural Support Programme. The new project has been launched simultaneously in all four provinces of Pakistan on 25000 acres of salt-affected land. Under this project seeds of salt tolerant crop varieties wheat, cotton, rice, castor, brassica and barley and saplings of trees/shrubs, e.g. Acacia ampliceps, A. nilotica, Casuarina glauca, ber, jaman, etc selected for development work in various institutions of Pakistan are being provided to farmers. Know-how on new irrigation techniques like bed-and-corrugation and bed-and-furrow, agronomic practices like laser land leveling, planting on beds and in auger holes and soil/water amendment practices (use of gypsum and mineral acids) are being shared with farmers. These interventions are quite efficient, save water up to 40% and enable farmers to utilize bad quality water. In general, farmers are being familiarized with prevalent animal diseases, nutritional problems and prophylactic techniques. They are being helped in developing Saline

Numerical Study on Effects of Coastline Change on Salinity variation in the Liao River Estuary

Science.gov (United States)

Li, Xin; Zhang, Xue-qing; Zhao, Yang; Li, Qing-zhen; Yu, Jin-zhen

2017-08-01

A 3D numerical model is used to simulate the effect of coastline change on salinity distribution variation in the Liao River Estuary (LHE), China, consists of shallow channel and extensive tidal flat. Simulations are run with reclamation and land-ocean interaction to evaluate their effects on salinity transport for LHE. It is so evident to express the salinity diurnal varying with tide rather than the amount of runoff discharge; the LHE is always the rising tide advantage free of reclamation. To succinctly quantify the asymmetry degree of salinity distribution across the Gaizhou beach (GZB), the calculated parameter of low-salinity area is chosen. For dry seasons, such as May, the amplitude of its scale is from 209.54 km2 reducing to 185.6 km2. More interestingly, it demonstrates the variation shape divided into increasing at the west of GZB and decreasing in the east, varying from 7.4 to 20.9 km2, especially the east of GZB. Despite the trend is basically consistent with flood seasons, the scale is 1.6 times higher than dry seasons. Reclamation has impact on low-salinity area variation enhanced coastal change influences on salinity distribution are less distinctive, but significant in ecological sustainability just like fishery breeding stability.

Theory of the isotope effect in superconducting compounds

International Nuclear Information System (INIS)

Culetto, F.J.; Rainer, D.

1978-05-01

We present a theoretical analysis of the isotope effect on the superconducting transition temperature. Our method is to calculate via formal perturbation theory the response of the transition temperature to small changes of the masses of the various constituents of the compound. We discuss the relation between the isotope effect and various more fundamental parameters in strong coupling superconductors. As illustrative examples, we consider the systems Pd-H(D) alloys and the binary Chevrel phase superconductor Mo 6 Se 8 , and show that analysis of the isotope effect can yield useful information concerning interaction mechanisms in these compounds. (orig.)

Saline instillation before tracheal suctioning decreases the incidence of ventilator-associated pneumonia.

Science.gov (United States)

Caruso, Pedro; Denari, Silvia; Ruiz, Soraia A L; Demarzo, Sergio E; Deheinzelin, Daniel

2009-01-01

To compare the incidence of ventilator-associated pneumonia (VAP) with or without isotonic saline instillation before tracheal suctioning. As a secondary objective, we compared the incidence of endotracheal tube occlusion and atelectasis. Randomized clinical trial. The study was conducted in a medical surgical intensive care unit of an oncologic hospital. We selected consecutive patients needing mechanical ventilation for >72 hrs. Patients were allocated into two groups: a saline group that received instillation of 8 mL of saline before tracheal suctioning and a control group which did not. VAP was diagnosed based on clinical suspicion and confirmed by bronchoalveolar lavage quantitative culture. The incidence of atelectasis on daily chest radiography and endotracheal tube occlusions were recorded. The sample size was calculated to a power of 80% and a type I error probability of 5%. One hundred thirty patients were assigned to the saline group and 132 to the control group. The baseline demographic variables were similar between groups. The rate of clinically suspected VAP was similar in both groups. The incidence of microbiological proven VAP was significantly lower in the saline group (23.5% x 10.8%; p = 0.008) (incidence density/1.000 days of ventilation 21.22 x 9.62; p < 0.01). Using the Kaplan-Meier curve analysis, the proportion of patients remaining without VAP was higher in the saline group (p = 0.02, log-rank test). The relative risk reduction of VAP in the saline instillation group was 54% (95% confidence interval, 18%-74%) and the number needed to treat was eight (95% confidence interval, 5-27). The incidence of atelectases and endotracheal tube occlusion were similar between groups. Instillation of isotonic saline before tracheal suctioning decreases the incidence of microbiological proven VAP.

Description of input and examples for PHREEQC version 3: a computer program for speciation, batch-reaction, one-dimensional transport, and inverse geochemical calculations

Science.gov (United States)

Parkhurst, David L.; Appelo, C.A.J.

2013-01-01

PHREEQC version 3 is a computer program written in the C and C++ programming languages that is designed to perform a wide variety of aqueous geochemical calculations. PHREEQC implements several types of aqueous models: two ion-association aqueous models (the Lawrence Livermore National Laboratory model and WATEQ4F), a Pitzer specific-ion-interaction aqueous model, and the SIT (Specific ion Interaction Theory) aqueous model. Using any of these aqueous models, PHREEQC has capabilities for (1) speciation and saturation-index calculations; (2) batch-reaction and one-dimensional (1D) transport calculations with reversible and irreversible reactions, which include aqueous, mineral, gas, solid-solution, surface-complexation, and ion-exchange equilibria, and specified mole transfers of reactants, kinetically controlled reactions, mixing of solutions, and pressure and temperature changes; and (3) inverse modeling, which finds sets of mineral and gas mole transfers that account for differences in composition between waters within specified compositional uncertainty limits. Many new modeling features were added to PHREEQC version 3 relative to version 2. The Pitzer aqueous model (pitzer.dat database, with keyword PITZER) can be used for high-salinity waters that are beyond the range of application for the Debye-Hückel theory. The Peng-Robinson equation of state has been implemented for calculating the solubility of gases at high pressure. Specific volumes of aqueous species are calculated as a function of the dielectric properties of water and the ionic strength of the solution, which allows calculation of pressure effects on chemical reactions and the density of a solution. The specific conductance and the density of a solution are calculated and printed in the output file. In addition to Runge-Kutta integration, a stiff ordinary differential equation solver (CVODE) has been included for kinetic calculations with multiple rates that occur at widely different time scales

Charge radii of neutron-deficient Ca isotopes

Science.gov (United States)

Miller, A. J.; Minamisono, K.; Klose, A.; Everett, N.; Kalman, C.; Powel, R. C.; Watkins, J.; Garand, D.; Sumithrarachchi, C.; Krämer, J.; Maa, B.; Nörtershäuser, W.; Rossi, D. M.; Kujawa, C.; Pineda, S.; Lantis, J.; Liu, Y.; Mantica, P. F.; Pearson, M. R.

2017-09-01

Nucleon shell closures are generally associated with a local minimum in mean-square charge radii, 〈r2 〉 , along an isotopic chain. The 〈r2 〉 of 18Ar and 19K isotopes, however, do not show this signature at the N = 20 neutron shell closure. To gain a microscopic understanding of this abnormal behavior, measurements of 〈r2 〉 of neutron-deficient Ca isotopes below N = 20 have been proposed at the BEam COoling and LAser spectroscopy (BECOLA) facility at NSCL/MSU. Preliminary results will be presented and the deduced charge radii will be compared to theoretical calculations and the trends in the nearby isotopic chains. Work supported in part by NSF Grant PHY-15-65546, U.S. DOE Grant DE-NA0002924 and by the Deutsche Forschungsgemeinschaft through Grant SFB 1245.

Rapid estimation of aquifer salinity structure from oil and gas geophysical logs

Science.gov (United States)

Shimabukuro, D.; Stephens, M.; Ducart, A.; Skinner, S. M.

2016-12-01

We describe a workflow for creating aquifer salinity maps using Archie's equation for areas that have geophysical data from oil and gas wells. We apply this method in California, where geophysical logs are available in raster format from the Division of Oil, Gas, and Geothermal Resource (DOGGR) online archive. This method should be applicable to any region where geophysical logs are readily available. Much of the work is controlled by computer code, allowing salinity estimates for new areas to be rapidly generated. For a region of interest, the DOGGR online database is scraped for wells that were logged with multi-tool suites, such as the Platform Express or Triple Combination Logging Tools. Then, well construction metadata, such as measured depth, spud date, and well orientation, is attached. The resultant local database allows a weighted criteria selection of wells that are most likely to have the shallow resistivity, deep resistivity, and density porosity measurements necessary to calculate salinity over the longest depth interval. The algorithm can be adjusted for geophysical log availability for older well fields and density of sampling. Once priority wells are identified, a student researcher team uses Neuralog software to digitize the raster geophysical logs. Total dissolved solid (TDS) concentration is then calculated in clean, wet sand intervals using the resistivity-porosity method, a modified form of Archie's equation. These sand intervals are automatically selected using a combination of spontaneous potential and the difference in shallow resistivity and deep resistivity measurements. Gamma ray logs are not used because arkosic sands common in California make it difficult to distinguish sand and shale. Computer calculation allows easy adjustment of Archie's parameters. The result is a semi-continuous TDS profile for the wells of interest. These profiles are combined and contoured using standard 3-d visualization software to yield preliminary salinity

Origin and evolution of formation water at the Jujo-Tecominoacan oil reservoir, Gulf of Mexico. Part 2: Isotopic and field-production evidence for fluid connectivity

Energy Technology Data Exchange (ETDEWEB)

Birkle, Peter, E-mail: birkle@iie.org.mx [Instituto de Investigaciones Electricas (IIE), Gerencia de Geotermia, Cuernavaca 62490, Morelos (Mexico); Garcia, Bernardo Martinez; Milland Padron, Carlos M. [PEMEX Exploracion y Produccion, Region Sur, Activo Integral Bellota-Jujo, Diseno de Explotacion, Cardenas, Tabasco (Mexico); Eglington, Bruce M. [Saskatchewan Isotope Laboratory, University of Saskatchewan, Saskatoon, Canada SK S7N 5E2 (Canada)

2009-04-15

The chemical and isotopic characterization of formation water from 18 oil production wells, extracted from 5200 to 6100 m b.s.l. at the Jujo-Tecominoacan carbonate reservoir in SE-Mexico, and interpretations of historical production records, were undertaken to determine the origin and hydraulic behavior of deep groundwater systems. The infiltration of surface water during Late Pleistocene to Early Holocene time is suggested by {sup 14}C-concentrations from 2.15 to 31.86 pmC, and by {sup 87}Sr/{sup 86}Sr-ratios for high-salinity formation water (0.70923-0.70927) that are close to the composition of Holocene to modern seawater. Prior to infiltration, the super-evaporation of seawater reached maximum TDS concentrations of 385 g/L, with lowest {delta}{sup 18}O values characterizing the most hypersaline samples. Minor deviations of formation water and dolomite host rocks from modern and Jurassic {sup 87}Sr/{sup 86}Sr-seawater composition, respectively, suggest ongoing water-rock interaction, and partial isotopic equilibration between both phases. The abundance of {sup 14}C in all sampled formation water, {sup 87}Sr/{sup 86}Sr-ratios for high-salinity water close to Holocene - present seawater composition, a water salinity distribution that is independent of historic water-cut, and a total water extraction volume of 2.037 MMm{sup 3} (1/83-4/07) excludes a connate, oil-leg origin for the produced water of the Jurassic-Cretaceous mudstone-dolomite sequence. Temporal fluctuations of water chemistry in production intervals, the accelerated migration of water fronts from the reservoir flanks, and isotopic mixing trends between sampled wells confirms the existence of free aquifer water below oil horizons. Vertical and lateral hydraulic mobility has probably been accelerated by petroleum extraction. The combination of interpreting historical fluctuations of salinity and water percentage in production wells with chemical-isotopic analysis of formation water resulted in a

Origin and evolution of formation water at the Jujo-Tecominoacan oil reservoir, Gulf of Mexico. Part 2: Isotopic and field-production evidence for fluid connectivity

International Nuclear Information System (INIS)

Birkle, Peter; Garcia, Bernardo Martinez; Milland Padron, Carlos M.; Eglington, Bruce M.

2009-01-01

The chemical and isotopic characterization of formation water from 18 oil production wells, extracted from 5200 to 6100 m b.s.l. at the Jujo-Tecominoacan carbonate reservoir in SE-Mexico, and interpretations of historical production records, were undertaken to determine the origin and hydraulic behavior of deep groundwater systems. The infiltration of surface water during Late Pleistocene to Early Holocene time is suggested by 14 C-concentrations from 2.15 to 31.86 pmC, and by 87 Sr/ 86 Sr-ratios for high-salinity formation water (0.70923-0.70927) that are close to the composition of Holocene to modern seawater. Prior to infiltration, the super-evaporation of seawater reached maximum TDS concentrations of 385 g/L, with lowest δ 18 O values characterizing the most hypersaline samples. Minor deviations of formation water and dolomite host rocks from modern and Jurassic 87 Sr/ 86 Sr-seawater composition, respectively, suggest ongoing water-rock interaction, and partial isotopic equilibration between both phases. The abundance of 14 C in all sampled formation water, 87 Sr/ 86 Sr-ratios for high-salinity water close to Holocene - present seawater composition, a water salinity distribution that is independent of historic water-cut, and a total water extraction volume of 2.037 MMm 3 (1/83-4/07) excludes a connate, oil-leg origin for the produced water of the Jurassic-Cretaceous mudstone-dolomite sequence. Temporal fluctuations of water chemistry in production intervals, the accelerated migration of water fronts from the reservoir flanks, and isotopic mixing trends between sampled wells confirms the existence of free aquifer water below oil horizons. Vertical and lateral hydraulic mobility has probably been accelerated by petroleum extraction. The combination of interpreting historical fluctuations of salinity and water percentage in production wells with chemical-isotopic analysis of formation water resulted in a successful method to distinguish four groundwater bodies

Numerical assessment of the origin of deep salinity in a low permeability fractured medium

International Nuclear Information System (INIS)

Guimera, Jordi; Ruiz, Eduardo; Luna, Miguel; Arcos, David; Domenech, Cristina; Jordana, Salvador; Saegusa, Hiromitsu; Iwatsuki, Teruki

2007-01-01

Many possible origins have been proposed for the saline groundwater observed in many deep geological environments. In particular, samples obtained from deep boreholes located in granite at the Mizunami Underground Research Laboratory in Central Japan show total dissolved solids increasing to 50 mmol/L at depths below 800 m. Different hypothesis have been formulated to explain the observed fluid composition, among them, long-term water-rock interaction, mixing with residual fluids of magmatic origin and relict seawater dating from Miocene times. A review of the hydrochemical and isotopic data suggests that the three above hypotheses may be valid, at least to different degrees, or that processes acting over more recent geological times may be involved. The origin of the salinity was assessed by simulating land emersion by means of changing the upper recharge boundary. In this manner the Miocene seawater was modeled as being continually mixed with fresh water until the present time. The effects of different retardation processes were considered by varying factors such as matrix diffusion and fracture conductivity. Finally, geochemical reactions reproduced trends in major ions and master variables. This study shows that the salinity observed in the boreholes can be explained qualitatively as residual Miocene age seawater subjected to alteration due to long-term contact with the host material and continuous mixing with meteoric groundwater. (authors)

Dextrose saline compared with normal saline rehydration of hyperemesis gravidarum: a randomized controlled trial.

Science.gov (United States)

Tan, Peng Chiong; Norazilah, Mat Jin; Omar, Siti Zawiah

2013-02-01

To compare 5% dextrose-0.9% saline against 0.9% saline solution in the intravenous rehydration of hyperemesis gravidarum. Women at their first hospitalization for hyperemesis gravidarum were enrolled on admission to the ward and randomly assigned to receive either 5% dextrose-0.9% saline or 0.9% saline by intravenous infusion at a rate 125 mL/h over 24 hours in a double-blind trial. All participants also received thiamine and an antiemetic intravenously. Oral intake was allowed as tolerated. Primary outcomes were resolution of ketonuria and well-being (by 10-point visual numerical rating scale) at 24 hours. Nausea visual numerical rating scale scores were obtained every 8 hours for 24 hours. Persistent ketonuria rates after the 24-hour study period were 10 of 101 (9.9%) compared with 11 of 101 (10.9%) (P>.99; relative risk 0.9, 95% confidence interval 0.4-2.2) and median (interquartile range) well-being scores at 24 hours were 9 (8-10) compared with 9 (8-9.5) (P=.73) in the 5% dextrose-0.9% saline and 0.9% saline arms, respectively. Repeated measures analysis of variance of the nausea visual numerical rating scale score as assessed every 8 hours during the 24-hour study period showed a significant difference in favor of the 5% dextrose-0.9% saline arm (P=.046) with the superiority apparent at 8 and 16 hours, but the advantage had dissipated by 24 hours. Secondary outcomes of vomiting, resolution of hyponatremia, hypochloremia and hypokalemia, length of hospitalization, duration of intravenous antiemetic, and rehydration were not different. Intravenous rehydration with 5% dextrose-0.9% saline or 0.9% saline solution in women hospitalized for hyperemesis gravidarum produced similar outcomes. ISRCTN Register, www.controlled-trials.com/isrctn, ISRCTN65014409. I.

Impact of statistical uncertainty of the neutron spectrum in the isotopic evolution of fuel

International Nuclear Information System (INIS)

Ortega, P.

2012-01-01

The results obtained and presented in this study for different calculation conditions (number of stories, number of steps burning, etc.) and their simultaneous impact on neutron spectrum and isotopic composition and a methodology is proposed to determine the minimum parameters for calculation given uncertainty in the results of isotopic composition with high burnup, both UO 2 and MOX fuel.

Precision Mass Measurement of Argon Isotopes

CERN Multimedia

Lunney, D

2002-01-01

% IS388\\\\ \\\\ A precision mass measurement of the neutron-deficient isotopes $^{32,33,34}$Ar is proposed. Mass values of these isotopes are of importance for: a) a stringent test of the Isobaric-Multiplet- Mass-Equation, b) a verification of the correctness of calculated charge-dependent corrections as used in super-allowed $\\beta$- decay studies aiming at a test of the CVC hypothesis, and c) the determination of the kinematics in electron-neutrino correlation experiments searching for scalar currents in weak interaction. The measurements will be carried out with the ISOLTRAP Penning trap mass spectrometer.

Oxygen isotope fractionation in uranium oxides

International Nuclear Information System (INIS)

Zheng Yongfei

1995-01-01

Thermodynamic oxygen isotope factors for uranium oxides have been calculated by means of the modified increment method. The sequence of 18 O-enrichment in the uranium oxides with respect to the common rock-forming minerals is predicted as follows: spinel 3 < illite. Two sets of self-consistent fractionation factors between the uranium oxides and water and between the uranium oxides and the other minerals have been obtained for 0∼1200 degree C. The theoretical results are applicable to the isotopic geothermometry of uranium ores when pairing with other gangue minerals in hydrothermal uranium deposits

HAMMER, 1-D Multigroup Neutron Transport Infinite System Cell Calculation for Few-Group Diffusion Calculation

International Nuclear Information System (INIS)

Honeck, H.C.

1984-01-01

1 - Description of problem or function: HAMMER performs infinite lattice, one-dimensional cell multigroup calculations, followed (optionally) by one-dimensional, few-group, multi-region reactor calculations with neutron balance edits. 2 - Method of solution: Infinite lattice parameters are calculated by means of multigroup transport theory, composite reactor parameters by few-group diffusion theory. 3 - Restrictions on the complexity of the problem: - Cell calculations - maxima of: 30 thermal groups; 54 epithermal groups; 20 space points; 20 regions; 18 isotopes; 10 mixtures; 3 thermal up-scattering mixtures; 200 resonances per group; no overlap or interference; single level only. - Reactor calculations - maxima of : 40 regions; 40 mixtures; 250 space points; 4 groups

Water cycle and salinity dynamics in the mangrove forests of Europa and Juan de Nova Islands, southwest Indian Ocean.

Science.gov (United States)

Lambs, Luc; Mangion, Perrine; Mougin, Eric; Fromard, François

2016-01-30

The functioning of mangrove forests found on small coralline islands is characterized by limited freshwater inputs. Here, we present data on the water cycling of such systems located on Europa and Juan de Nova Islands, Mozambique Channel. In order to better understand the water cycle and mangrove growth conditions, we have analysed the hydrological and salinity dynamics of the systems by gauge pressure and isotopic tracing (δ18O and δ2H values). Both islands have important seawater intrusion as measured by the water level change and the high salinities in the karstic ponds. Europa Island displays higher salinity stress, with its inner lagoon, but presents a pluri-specific mangrove species formation ranging from shrub to forest stands. No freshwater signal could be detected around the mangrove trees. On Juan de Nova Island, the presence of sand and detrital sediment allows the storage of some amount of rainfall to form a brackish groundwater. The mangrove surface area is very limited with only small mono-specific stands being present in karstic depression. On the drier Europa Island, the salinity of all the water points is equal to or higher than that of the seawater, and on Juan de Nova the groundwater salinity is lower (5 to 20 PSU). This preliminary study shows that the karstic pothole mangroves exist due to the sea connection through the fractured coral and the high tidal dynamics.

Production of medical radioactive isotopes using KIPT electron driven subcritical facility

International Nuclear Information System (INIS)

Talamo, Alberto; Gohar, Yousry

2008-01-01

Kharkov Institute of Physics and Technology (KIPT) of Ukraine in collaboration with Argonne National Laboratory (ANL) has a plan to construct an electron accelerator driven subcritical assembly. One of the facility objectives is the production of medical radioactive isotopes. This paper presents the ANL collaborative work performed for characterizing the facility performance for producing medical radioactive isotopes. First, a preliminary assessment was performed without including the self-shielding effect of the irradiated samples. Then, more detailed investigation was carried out including the self-shielding effect, which defined the sample size and location for producing each medical isotope. In the first part, the reaction rates were calculated as the multiplication of the cross section with the unperturbed neutron flux of the facility. Over fifty isotopes have been considered and all transmutation channels are used including (n, γ), (n, 2n), (n, p), and (γ, n). In the second part, the parent isotopes with high reaction rate were explicitly modeled in the calculations. Four irradiation locations were considered in the analyses to study the medical isotope production rate. The results show the self-shielding effect not only reduces the specific activity but it also changes the irradiation location that maximizes the specific activity. The axial and radial distributions of the parent capture rates have been examined to define the irradiation sample size of each parent isotope

Production of medical radioactive isotopes using KIPT electron driven subcritical facility

Energy Technology Data Exchange (ETDEWEB)

Talamo, Alberto [Nuclear Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439 (United States)], E-mail: alby@anl.gov; Gohar, Yousry [Nuclear Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439 (United States)

2008-05-15

Kharkov Institute of Physics and Technology (KIPT) of Ukraine in collaboration with Argonne National Laboratory (ANL) has a plan to construct an electron accelerator driven subcritical assembly. One of the facility objectives is the production of medical radioactive isotopes. This paper presents the ANL collaborative work performed for characterizing the facility performance for producing medical radioactive isotopes. First, a preliminary assessment was performed without including the self-shielding effect of the irradiated samples. Then, more detailed investigation was carried out including the self-shielding effect, which defined the sample size and location for producing each medical isotope. In the first part, the reaction rates were calculated as the multiplication of the cross section with the unperturbed neutron flux of the facility. Over fifty isotopes have been considered and all transmutation channels are used including (n, {gamma}), (n, 2n), (n, p), and ({gamma}, n). In the second part, the parent isotopes with high reaction rate were explicitly modeled in the calculations. Four irradiation locations were considered in the analyses to study the medical isotope production rate. The results show the self-shielding effect not only reduces the specific activity but it also changes the irradiation location that maximizes the specific activity. The axial and radial distributions of the parent capture rates have been examined to define the irradiation sample size of each parent isotope.

Production of medical radioactive isotopes using KIPT electron driven subcritical facility.

Science.gov (United States)

Talamo, Alberto; Gohar, Yousry

2008-05-01

Kharkov Institute of Physics and Technology (KIPT) of Ukraine in collaboration with Argonne National Laboratory (ANL) has a plan to construct an electron accelerator driven subcritical assembly. One of the facility objectives is the production of medical radioactive isotopes. This paper presents the ANL collaborative work performed for characterizing the facility performance for producing medical radioactive isotopes. First, a preliminary assessment was performed without including the self-shielding effect of the irradiated samples. Then, more detailed investigation was carried out including the self-shielding effect, which defined the sample size and location for producing each medical isotope. In the first part, the reaction rates were calculated as the multiplication of the cross section with the unperturbed neutron flux of the facility. Over fifty isotopes have been considered and all transmutation channels are used including (n, gamma), (n, 2n), (n, p), and (gamma, n). In the second part, the parent isotopes with high reaction rate were explicitly modeled in the calculations. Four irradiation locations were considered in the analyses to study the medical isotope production rate. The results show the self-shielding effect not only reduces the specific activity but it also changes the irradiation location that maximizes the specific activity. The axial and radial distributions of the parent capture rates have been examined to define the irradiation sample size of each parent isotope.

Isotopic, hydrochemical, and hydrogeological study of deep aquifer of Sfax: First results

International Nuclear Information System (INIS)

Maliki, M. A.; Zouari, K.; Amouri, M.

1996-01-01

The water of the chlorinated sodic with chemical facies deep aquifer of Sfax presents a difference on the level of mineralization between the northern sector with a relatively weak salin charge (average of 3,5 g/l) and the southern sector with an important mineralization (about 10g/l). The mineralization of water in linked to dissolution phenomena. Based on the first isotopic results, it seems that the present refill of the deep aquifer of Sfax is very weak (author)

Shape coexistence in neutron-deficient Hg isotopes studied via lifetime measurements in $^{184,186}$Hg and two-state mixing calculations

CERN Document Server

Gaffney, L P; Page, R.D.; Grahn, T.; Scheck, M.; Butler, P.A.; Bertone, P.F.; Bree, N.; Carroll, R.J.; Carpenter, M.P.; Chiara, C.J.; Dewald, A.; Filmer, F.; Fransen, C.; Huyse, M.; Janssens, R.V.F.; Joss, D.T.; Julin, R.; Kondev, F.G.; Nieminen, P.; Pakarinen, J.; Rigby, S.V.; Rother, W.; Van Duppen, P.; Watkins, H.V.; Wrzosek-Lipska, K.; Zhu, S.

2014-01-01

The neutron-deficient mercury isotopes, $^{184,186}$Hg, were studied with the Recoil Distance Doppler Shift (RDDS) method using the Gammasphere array and the K\\"oln Plunger device. The Differential Decay Curve Method (DDCM) was employed to determine the lifetimes of the yrast states in $^{184,186}$Hg. An improvement on previously measured values of yrast states up to $8^{+}$ is presented as well as first values for the $9_{3}$ state in $^{184}$Hg and $10^{+}$ state in $^{186}$Hg. $B(E2)$ values are calculated and compared to a two-state mixing model which utilizes the variable moment of inertia (VMI) model, allowing for extraction of spin-dependent mixing strengths and amplitudes.

Isotope effects in gas-phase chemical reactions and photodissociation processes: Overview

International Nuclear Information System (INIS)

Kaye, J.A.

1992-01-01

The origins of isotope effects in equilibrium and non-equilibrium chemical processes are reviewed. In non-equilibrium processes, attention is given to isotope effects in simple bimolecular reactions, symmetry-related reactions, and photodissociation processes. Recent examples of isotope effects in these areas are reviewed. Some indication of other scientific areas for which measurements and/or calculations of isotope effects are used is also given. Examples presented focus on neutral molecule chemistry and in many cases complement examples considered in greater detail in the other chapters of this volume

Liquid and gas chromatography coupled to isotope ratio mass spectrometry for the determination of 13C-valine isotopic ratios in complex biological samples.

Science.gov (United States)

Godin, Jean-Philippe; Breuillé, Denis; Obled, Christiane; Papet, Isabelle; Schierbeek, Henk; Hopfgartner, Gérard; Fay, Laurent-Bernard

2008-10-01

On-line gas chromatography-combustion-isotope ratio mass spectrometry (GC-C-IRMS) is commonly used to measure isotopic ratios at natural abundance as well as for tracer studies in nutritional and medical research. However, high-precision (13)C isotopic enrichment can also be measured by liquid chromatography-isotope ratio mass spectrometry (LC-IRMS). Indeed, LC-IRMS can be used, as shown by the new method reported here, to obtain a baseline separation and to measure (13)C isotopic enrichment of underivatised amino acids (Asp, Thr-Ser, Glu, Pro, Gly, Ala, Cys and Val). In case of Val, at natural abundance, the SD(delta(13)C) reported with this method was found to be below 1 per thousand . Another key feature of the new LC-IRMS method reported in this paper is the comparison of the LC-IRMS approach with the conventional GC-C-IRMS determination. To perform this comparative study, isotopic enrichments were measured from underivatised Val and its N(O, S)-ethoxycarbonyl ethyl ester derivative. Between 0.0 and 1.0 molar percent excess (MPE) (delta(13)C= -12.3 to 150.8 per thousand), the calculated root-mean-square (rms) of SD was 0.38 and 0.46 per thousand and the calculated rms of accuracy was 0.023 and 0.005 MPE, respectively, for GC-C-IRMS and LC-IRMS. Both systems measured accurately low isotopic enrichments (0.002 atom percent excess (APE)) with an SD (APE) of 0.0004. To correlate the relative (delta(13)C) and absolute (atom%, APE and MPE) isotopic enrichment of Val measured by the GC-C-IRMS and LC-IRMS devices, mathematical equations showing the slope and intercept of the curves were established and validated with experimental data between 0.0 to 2.3 MPE. Finally, both GC-C-IRMS and LC-IRMS instruments were also used to assess isotopic enrichment of protein-bound (13)C-Val in tibial epiphysis in a tracer study performed in rats. Isotopic enrichments measured by LC-IRMS and GC-C-IRMS were not statistically different (p>0.05). The results of this work indicate that

Salinity Trends in the Upper Colorado River Basin Upstream From the Grand Valley Salinity Control Unit, Colorado, 1986-2003

Science.gov (United States)

Leib, Kenneth J.; Bauch, Nancy J.

2008-01-01

In 1974, the Colorado River Basin Salinity Control Act was passed into law. This law was enacted to address concerns regarding the salinity content of the Colorado River. The law authorized various construction projects in selected areas or 'units' of the Colorado River Basin intended to reduce the salinity load in the Colorado River. One such area was the Grand Valley Salinity Control Unit in western Colorado. The U. S. Geological Survey has done extensive studies and research in the Grand Valley Salinity Control Unit that provide information to aid the U.S. Bureau of Reclamation and the Natural Resources Conservation Service in determining where salinity-control work may provide the best results, and to what extent salinity-control work was effective in reducing salinity concentrations and loads in the Colorado River. Previous studies have indicated that salinity concentrations and loads have been decreasing downstream from the Grand Valley Salinity Control Unit, and that the decreases are likely the result of salinity control work in these areas. Several of these reports; however, also document decreasing salinity loads upstream from the Grand Valley Salinity Control Unit. This finding was important because only a small amount of salinity-control work was being done in areas upstream from the Grand Valley Salinity Control Unit at the time the findings were reported (late 1990?s). As a result of those previous findings, the U.S. Bureau of Reclamation entered into a cooperative agreement with the U.S. Geological Survey to investigate salinity trends in selected areas bracketing the Grand Valley Salinity Control Unit and regions upstream from the Grand Valley Salinity Control Unit. The results of the study indicate that salinity loads were decreasing upstream from the Grand Valley Salinity Control Unit from 1986 through 2003, but the rates of decrease have slowed during the last 10 years. The average rate of decrease in salinity load upstream from the Grand Valley

Isotope hydrology of catchment basins: lithogenic and cosmogenic isotopic systems

Energy Technology Data Exchange (ETDEWEB)

Nimz, G. J., LLNL

1998-06-01

also be treated as a mostly closed system for mass balance considerations. It is the near closure of the system that permits well- constrained chemical mass balance calculations to be made. These calculations generally focus of lithogenic solutes, and therefore in our discussions of lithogenic nuclides in the paper, the concept of chemical mass balance in a nearly dosed system will play an important role. Examination of the isotopic compositions of solutes provides a better understanding of the variety of processes controlling mass balance. It is with this approach that we examined the variety of processes occurring within the catchment system, such as weathering and soil production, generation of stormflow and streamflow (hydrograph separation), movement of soil pore water, groundwater flow, and the overall processes involved with basinal water balance. In this paper, the term `nuclide` will be used when referring to a nuclear species that contains a particular number of protons and neutrons. The term is not specific to any element. The term `isotope` will be used to distinguish nuclear species of a given element (atoms with the same number of protons). That is to say, there are many nuclides in nature - for example, {sup 36}Cl, {sup 87}Sr, {sup 238}U; the element has four naturally-occurring isotopes - {sup 87}Sr, and {sup 88}Sr. This paper will first discuss the general principles that underlie the study of lithogenic and cosmogenic nuclides in hydrology, and provide references to some of the more important studies applying these principles and nuclides. We then turn in the second section to a discussion of their specific applications in catchment- scale systems. The final section of this paper discusses new directions in the application of lithogenic and cosmogenic nuclides to catchment hydrology, with some thoughts concerning possible applications that still remain unexplored.

Stable isotopic and mineralogical studies of hydrothermal alteration at Arima Spa, Southwest Japan

International Nuclear Information System (INIS)

Masuda, Harue; Osaka City Univ.; Sakai, Hitoshi; Chiba, Hitoshi; Matsuhisa, Yukihiro; Nakamura, Takeshi

1986-01-01

The waters of Arima Spa, Southwest Japan, have high salinity (Cl = 54 g/kg) and high isotopic ratios (deltaD = -32, and delta 18 O = +10 per mille), and issue from shallow wells drilled into altered rhyolitic pyroclastic rocks of Cretaceous age. Alteration of the host rocks occurred in two stages. The earlier regional alteration stage is characterized by the presence of 2M- and 1M-type muscovite, albite, chlorite, calcite and epidote, whereas muscovite and Fe-chlorite formation at the expense of partly albitized plagioclase and altered biotite or hornblende occurred in the following hydrothermal stage. Pyrite, sphalerite, galena and siderite are present in the central part of the hydrothermal alteration zone. Oxygen and hydrogen isotopic ratios of secondary muscovite show that regional alteration proceeded under the meteoric circulation, and that the hydrothermal fluid for the second stage had chemical and stable isotopic characteristics of non-meteoric origin similar to the present-day Arima brine. The oxygen and to a lesser extent the hydrogen isotopic ratios of the muscovite rapidly decrease with increasing distance from the central zone of hydrothermal alteration. The isotopic variation is best interpreted as reflecting rapidly decreasing fluid/rock ratios with increasing distance of fluid penetration from the narrow hydrothermal alteration zone into the surrounding area. The results are discussed. (author)

Kinetics of isotopic exchanges by using radioactive indicators

International Nuclear Information System (INIS)

May, S.

1958-12-01

After having noticed that iodine 131 under the form of sodium iodide has always been used as radioactive indicator in the CEA atomic pile located in Chatillon, this research report recalls the counting technique and some historical aspects of the notion of isotopic exchange and qualitative works, and presents some generalities on isotopic exchanges (reactions and calculation of rate constants of order 1 and 2, calculation of activation energy, spectro-photometric studies, Walden inversion, alkaline hydrolysis, influence of solvent on exchange kinetics, influence of the nature of the mineral halide). The author then addresses exchanges in aliphatic series (exchange with sodium iodide and with molecular iodine), exchanges in olefin series, exchanges in alicyclic series, and exchanges in aromatic series

Comparisons between shell-model calculations, seniority truncation, and quasiparticle approximations: Application to the odd Ni isotopes and odd N = 82 isotones

International Nuclear Information System (INIS)

Losano, L.; Dias, H.; Krmpotic, F.; Wildenthal, B.H.

1988-01-01

A detailed study of the results of correcting BCS approximation for the effects of particle-number projection and blocking has been carried out. A low-seniority shell-model approximation was used as the frame of reference for investigating the mixing of one- and three-quasiparticle states in odd-mass Ni isotopes and in odd-mass N = 82 isotones. We discuss the results obtained for the energy spectra and electromagnetic decay properties. Effects of seniority-five configurations on the low-lying states have also been studied through the comparison of the low-seniority shell-model results with those which arose from the corresponding full shell-model calculations

Constraining calcium isotope fractionation (δ44/40Ca) in modern and fossil scleractinian coral skeleton

OpenAIRE

Pretet, Chloé; Samankassou, Elias; Felis, Thomas; Reynaud, Stéphanie; Böhm, Florian; Eisenhauer, Anton; Ferrier-Pagès, Christine; Gattuso, Jean-Pierre; Camoin, Gilbert

2013-01-01

The present study investigates the influence of environmental (temperature, salinity) and biological (growth rate, inter-generic variations) parameters on calcium isotope fractionation (δ44/40Ca) in scleractinian coral skeleton to better constrain this record. Previous studies focused on the δ44/40Ca record in different marine organisms to reconstruct seawater composition or temperature, but only few studies investigated corals. This study presents measurements performed on modern corals f...

A universal carbonate ion effect on stable oxygen isotope ratios in unicellular planktonic calcifying organisms

OpenAIRE

Ziveri, P.; Thoms, S.; Probert, I.; Geisen, M.; Langer, H.

2012-01-01

The oxygen isotopic composition (δ¹⁸O) of calcium carbonate of planktonic calcifying organisms is a key tool for reconstructing both past seawater temperature and salinity. The calibration of paloeceanographic proxies relies in general on empirical relationships derived from field experiments on extant species. Laboratory experiments have more often than not revealed that variables other than the target parameter influence the proxy signal, which makes proxy c...

Calculation of isotope burn-up and change in efficiency of absorbing elements of WWER-1000 control and protection system during burn-up

International Nuclear Information System (INIS)

Timofeeva, O.A.; Kurakin, K.U.

2006-01-01

The report deals with fast and thermal neutron flows distribution in structural elements of WWER-1000 fuel assembly and absorbing rods, determination of absorbing isotope burn-up and worth variation in WWER reactor control and protection system rods. Simulation of absorber rod burn-up is provided using code package SAPPHIRE 9 5 end RC W WER allowing detailed description of the core segment spatial model. Maximum burn-up of absorbing rods and respective worth variation of control and protection system rods is determined on the basis of a number of calculations considering known characteristics of fuel cycles (Authors)

Separation of nitrogen isotopes by laser light

Energy Technology Data Exchange (ETDEWEB)

Izawa, Y; Noguchi, Y; Yamanaka, C [Osaka Univ., Suita (Japan). Faculty of Engineering

1976-06-01

The separation experiment on nitrogen isotopes by laser light was made. First, the nitrogen isotopes of /sup 14/N and /sup 15/N in NH/sub 3/ molecules were separated by CO/sub 2/ laser and UV light. The separation factor and the enrichment factor were calculated. It was shown that their pressure dependence was in good agreement with the measured values. The separation factor of about 2% was obtained with UV light of 10/sup 6/W/cm/sup 2/.

Effect of temperature and salinity on stable isotopic composition of shallow water benthic foraminifera: A laboratory culture study

Digital Repository Service at National Institute of Oceanography (India)

Kurtarkar, S.R.; Linshy, V.N.; Saraswat, R.; Nigam, R.

in the laboratory. In the present work, shallow water benthic foraminiferal species, Rosalina sp. and Pararotalia nipponica were subjected to different combinations of seawater temperature (25�C to 35�C) and salinity (25 psu to 37 psu) in the laboratory to assess...

Saline agriculture in Mediterranean environments

Directory of Open Access Journals (Sweden)

Albino Maggio

2011-03-01

Full Text Available Salinization is increasingly affecting world's agricultural land causing serious yield loss and soil degradation. Understanding how we could improve crop productivity in salinized environments is therefore critical to meet the challenging goal of feeding 9.3 billion people by 2050. Our comprehension of fundamental physiological mechanisms in plant salt stress adaptation has greatly advanced over the last decades. However, many of these mechanisms have been linked to salt tolerance in simplified experimental systems whereas they have been rarely functionally proven in real agricultural contexts. In-depth analyses of specific crop-salinity interactions could reveal important aspects of plant salt stress adaptation as well as novel physiological/agronomic targets to improve salinity tolerance. These include the developmental role of root vs. shoot systems respect to water-ion homeostasis, morphological vs. metabolic contributions to stress adaptation, developmental processes vs. seasonal soil salinity evolution, residual effects of saline irrigation in non-irrigated crops, critical parameters of salt tolerance in soil-less systems and controlled environments, response to multiple stresses. Finally, beneficial effects of salinization on qualitative parameters such as stress-induced accumulation of high nutritional value secondary metabolites should be considered, also. In this short review we attempted to highlight the multifaceted nature of salinity in Mediterranean agricultural systems by summarizing most experimental activity carried out at the Department of Agricultural Engineering and Agronomy of University of Naples Federico II in the last few years.

Assessment of Bacterial Degradation of Aromatic Hydrocarbons in the Environment by Analysis of Stable Carbon Isotope Fractionation

Energy Technology Data Exchange (ETDEWEB)

Meckenstock, Rainer U. [Eberhard-Karls University of Tuebingen, Center for Applied Geoscience (Germany)], E-mail: rainer.meckenstock@uni-tuebingen.de; Morasch, Barbara [University of Konstanz, Faculty of Biology (Germany); Kaestner, Matthias; Vieth, Andrea; Richnow, Hans Hermann [Center for Environmental Research, Department of Remediation Research (Germany)

2002-05-15

{sup 13}C/{sup 12}C stable carbon isotope fractionation was used to assess biodegradation in contaminated aquifers with toluene as a model compound. Different strains of anaerobic bacteria (Thauera aromatica, Geobacter metallireducens, and the sulfate-reducing strain TRM1) showed consistent {sup 13}C/{sup 12}C carbon isotope fractionation with fractionation factors between {alpha}C = 1.0017 and 1.0018. In contrast, three cultures of aerobic organisms, using different mono- and dioxygenase enzyme systems to initiate toluene degradation, showed variable isotope fractionation factors of {alpha}C = 1.0027 (Pseudomonasputida strain mt-2), {alpha}C = 1.0011 (Ralstonia picketii), and{alpha}C = 1.0004 (Pseudomonas putida strain F1). The great variability of isotope fractionation between different aerobic bacterial strains suggests that interpretation of isotope data in oxic habitats can only be qualitative. A soil column was run as a model system for contaminated aquifers with toluene as the carbon source and sulfate as the electron acceptor and samples were taken at different ports along the column. Microbial toluene degradation was calculated based on the {sup 13}C/{sup 12}C isotope fractionation factors of the batch culture experiments together with the observed {sup 13}C/{sup 12}C isotope shifts of the residual toluene fractions. The calculated percentage of biodegradation, B, correlated well with the decreasing toluene concentrations at the sampling ports and indicated the increasing extent of biodegradation along the column. The theoretical toluene concentrations as calculated based on the isotope values matched the measured concentrations at the different sampling ports indicating that the Rayleigh equation can be used to calculate biodegradation in quasi closed systems based on measured isotope shifts. A similar attempt was performed to assess toluene degradation in a contaminated, anoxic aquifer. A transect of groundwater wells was monitored along the main

Assessment of groundwater pollution from ash ponds using stable and unstable isotopes around the Koradi and Khaperkheda thermal power plants (Maharashtra, India).

Science.gov (United States)

Voltaggio, M; Spadoni, M; Sacchi, E; Sanam, R; Pujari, P R; Labhasetwar, P K

2015-06-15

The impact on local water resources due to fly ash produced in the Koradi and Khaperkheda thermal power plants (district of Nagpur, Maharashtra - India) and disposed in large ponds at the surface was assessed through the study of environmental variation of ratios of stable and unstable isotopes. Analyses of oxygen and hydrogen isotopes suggest scarce interaction between the water temporarily stored in the ponds and the groundwater in the study area. Data also highlight that the high salinity of groundwater measured in the polluted wells is not due to evaporation, but to subsequent infiltration of stream waters draining from the ponds to the local aquifer. (87)Sr/(86)Sr values, when associated with Sr/Ca ratios, demonstrate the dominant role of waste waters coming from tens of brick kilns surrounding the pond sulfate pollution. Uranium isotopic analyses clearly show evidence of the interaction between groundwater and aquifer rocks, and confirm again the low influence of ash ponds. A new conceptual model based on the study of the isotopes of radium is also proposed and used to estimate residence times of groundwater in the area. This model highlights that high salinity cannot be in any case attributed to a prolonged water-rock interaction, but is due to the influence of untreated waste water of domestic or brick kiln origin on the shallow and vulnerable aquifers. Copyright © 2015 Elsevier B.V. All rights reserved.

Laser spectroscopy of neutron deficient gold and platinum isotopes

International Nuclear Information System (INIS)

Savard, G.

1988-03-01

A new method for on-line laser spectroscopy of radioactive atoms based on the resonant ionization spectroscopy of laser-desorbed radioactive samples has been devised. An experimental setup has been installed on-line at the ISOCELE mass separator in Orsay (France) and experiments have been performed on the region of transitional nuclei around Z=79. Isotopic shift measurements on four new isotopes 194 Au, 196 Au, 198 Au, 199 Au have been performed on gold and results on the neutron deficient isotopes down to 186 Au have been obtained confirming the nuclear ground-state shape transition from oblate to prolate between 187 Au and 186 Au. The first isotopic shift measurements on radioactive platinum isotopes have been obtained on 186 Pt, 188 Pt, 189 Pt. Indications of a shape transition have been observed between 186 Pt and 188 Pt. The extracted experimental changes in mean square charge radii δ 2 > A,A' along isotopic chains are compared to self-consistent Hartree-Fock plus BCS calculations

Geochemical and isotopic variations in shallow groundwater in areas of the Fayetteville Shale development, north-central Arkansas

International Nuclear Information System (INIS)

Warner, Nathaniel R.; Kresse, Timothy M.; Hays, Phillip D.; Down, Adrian; Karr, Jonathan D.; Jackson, Robert B.; Vengosh, Avner

2013-01-01

Highlights: • No evidence for shallow groundwater contamination in Fayetteville Shale, Arkansas. • Methane in groundwater is low and likely associated with shallow aquifer processes. • No relationship between methane and salinity in groundwater and shale-gas wells. • δ 13 C CH4 and δ 13 C DIC suggest biogenic origin for dissolved methane. • Water-aquifer rock interaction controls majority of water chemistry. - Abstract: Exploration of unconventional natural gas reservoirs such as impermeable shale basins through the use of horizontal drilling and hydraulic fracturing has changed the energy landscape in the USA providing a vast new energy source. The accelerated production of natural gas has triggered a debate concerning the safety and possible environmental impacts of these operations. This study investigates one of the critical aspects of the environmental effects; the possible degradation of water quality in shallow aquifers overlying producing shale formations. The geochemistry of domestic groundwater wells was investigated in aquifers overlying the Fayetteville Shale in north-central Arkansas, where approximately 4000 wells have been drilled since 2004 to extract unconventional natural gas. Monitoring was performed on 127 drinking water wells and the geochemistry of major ions, trace metals, CH 4 gas content and its C isotopes (δ 13 C CH4 ), and select isotope tracers (δ 11 B, 87 Sr/ 86 Sr, δ 2 H, δ 18 O, δ 13 C DIC ) compared to the composition of flowback-water samples directly from Fayetteville Shale gas wells. Dissolved CH 4 was detected in 63% of the drinking-water wells (32 of 51 samples), but only six wells exceeded concentrations of 0.5 mg CH 4 /L. The δ 13 C CH4 of dissolved CH 4 ranged from −42.3‰ to −74.7‰, with the most negative values characteristic of a biogenic source also associated with the highest observed CH 4 concentrations, with a possible minor contribution of trace amounts of thermogenic CH 4 . The majority of

Oxygen isotope geochemistry of Laurentide ice-sheet meltwater across Termination I

Science.gov (United States)

Vetter, Lael; Spero, Howard J.; Eggins, Stephen M.; Williams, Carlie; Flower, Benjamin P.

2017-12-01

We present a new method that quantifies the oxygen isotope geochemistry of Laurentide ice-sheet (LIS) meltwater across the last deglaciation, and reconstruct decadal-scale variations in the δ18O of LIS meltwater entering the Gulf of Mexico between ∼18 and 11 ka. We employ a technique that combines laser ablation ICP-MS (LA-ICP-MS) and oxygen isotope analyses on individual shells of the planktic foraminifer Orbulina universa to quantify the instantaneous δ18Owater value of Mississippi River outflow, which was dominated by meltwater from the LIS. For each individual O. universa shell, we measure Mg/Ca (a proxy for temperature) and Ba/Ca (a proxy for salinity) with LA-ICP-MS, and then analyze the same O. universa for δ18O using the remaining material from the shell. From these proxies, we obtain δ18Owater and salinity estimates for each individual foraminifer. Regressions through data obtained from discrete core intervals yield δ18Ow vs. salinity relationships with a y-intercept that corresponds to the δ18Owater composition of the freshwater end-member. Our data suggest that from 15.5 through 14.6 ka, estimated δ18Ow values of Mississippi River discharge from discrete core intervals range from -11‰ to -21‰ VSMOW, which is consistent with δ18O values from both regional precipitation and the low-elevation, southern margin of the LIS. During the Bølling and Allerød (14.0 through 13.3 ka), estimated δ18Ow values of Mississippi River discharge from discrete core intervals range from -22‰ to -38‰ VSMOW. These values suggest a dynamic melting history of different parts of the LIS, with potential contributions to Mississippi River outflow from both the low-elevation, southern margin of the LIS and high-elevation, high-latitude domes in the LIS interior that were transported to the ablation zone. Prior to ∼15.5 ka, the δ18Owater value of the Mississippi River was similar to that of regional precipitation or low-latitude LIS meltwater, but the Ba

Constraints of costal aquifer functioning in a deeply antropized area through a multi-isotope fingerprinting (Recife, Brazil)

Science.gov (United States)

Petelet-Giraud, Emmanuelle; Cary, Lise; Bertrand, Guillaume; Hirata, Ricardo; Martins, Veridiana; Montenegro, Suzana; Pauwels, Hélène; Kloppmann, Wolfram; Aquilina, Luc

2014-05-01

The Metropolitan Region of Recife (RMR) went through large changes of water and land uses over the last decades due to an increasing demographic pressure (1.5 M of inhabitants). These evolutions gave rise to numerous environmental consequences, such as a dramatic decline of the water levels, groundwater salinization and contamination. This degradation of natural resources is linked to the increase of water demand that is also punctually amplified by drought periods, inducing the construction of thousands of private wells. Recife city was built on an estuarine area, at the geological limits of the two sedimentary basins of Pernambuco (north of the city) and Paraíba (south of the city) separated by a famous shear zone (the Pernambuco lineament). Tectonic and sedimentary events involved in the genesis and evolution of these basins were mainly controlled by the opening of the Atlantic Ocean leading to the deposition of cretaceous sediments which now constitute the two main exploited aquifers, the Beberibe and Cabo aquifers. These two deep aquiferous formations are topped by the unconfined Boa Viagem aquifer of quaternary sediments. It is the most directly exposed to contamination, since it is connected to mangroves, rivers, estuaries and highly urbanized areas. Both the Beberibe and Cabo aquifers contain large clay levels and are separated by a rather continuous clayed formation which seems to play a consistent role of screen and to interfere in the hydraulic connections between the three aquifers. Previous isotopic studies have shown that recharge processes are similar in the aquifers, suggesting that exchanges may occur and may be modified or amplified by overexploitation. This very complex aquifer system is studied through more than 60 water samples, including some surface water samples from the main rivers. A methodology based on multi-isotopes fingerprinting is applied, including stable isotopes of the water molecule, strontium isotopes, boron isotopes, sulfur

Geochemical evolution of groundwater salinity at basin scale: a case study from Datong basin, Northern China.

Science.gov (United States)

Wu, Ya; Wang, Yanxin

2014-05-01

A hydrogeochemical investigation using integrated methods of stable isotopes ((18)O, (2)H), (87)Sr/(86)Sr ratios, Cl/Br ratios, chloride-mass balance, mass balance and hydrogeochemical modeling was conducted to interpret the geochemical evolution of groundwater salinity in Datong basin, northern China. The δ(2)H, δ(18)O ratios in precipitation exhibited a local meteoric water line of δ(2)H = 6.4 δ(18)O -5 (R(2) = 0.94), while those in groundwater suggested their meteoric origin in a historically colder climatic regime with a speculated recharge rate of less than 20.5 mm overall per year, in addition to recharge from a component of deep residual ancient lake water enriched with Br. According to the Sr isotope binary mixing model, the mixing of recharges from the Shentou karst springs (24%), the western margins (11%) and the eastern margins (65%) accounts for the groundwater from the deep aquifers of the down-gradient parts in the central basin is a possible mixing mechanism. In Datong, hydrolysis of silicate minerals is the most important hydrogeochemical process responsible for groundwater chemistry, in addition to dissolution of carbonate and evaporites. In the recharge areas, silicate chemical weathering is typically at the bisiallitization stage, while that in the central basin is mostly at the monosiallitization stage with limited evidence of being in equilibrium with gibbsite. Na exchange with bound Ca, Mg prevails at basin scale, and intensifies with groundwater salinity, while Ca, Mg exchange with bound Na locally occurs in the east pluvial and alluvial plains. Although groundwater salinity increases with the progress of water-rock/sediment interactions along the flow path, as a result of carbonate solubility control and continuous evapotranspiration, Na-HCO3 and Na-Cl-SO4 types of water are usually characterized respectively in the deep and the shallow aquifers of an inland basin with a silicate terrain in an arid climatic regime.

Temperature dependence of carbon isotope fractionation in CAM plants

International Nuclear Information System (INIS)

Deleens, E.; Treichel, I.; O'Leary, M.H.

1985-01-01

The carbon isotope fractionation associated with nocturnal malic acid synthesis in Kalanchoë daigremontiana and Bryophyllum tubiflorum was calculated from the isotopic composition of carbon-4 of malic acid, after appropriate corrections. In the lowest temperature treatment (17 degrees C nights, 23 degrees C days), the isotope fractionation for both plants is -4 per thousand (that is, malate is enriched in (13)C relative to the atmosphere). For K. daigremontiana, the isotope fractionation decreases with increasing temperature, becoming approximately 0 per thousand at 27 degrees C/33 degrees C. Detailed analysis of temperature effects on the isotope fractionation indicates that stomatal aperture decreases with increasing temperature and carboxylation capacity increases. For B. tubiflorum, the temperature dependence of the isotope fractionation is smaller and is principally attributed to the normal temperature dependences of the rates of diffusion and carboxylation steps. The small change in the isotopic composition of remaining malic acid in both species which is observed during deacidification indicates that malate release, rather than decarboxylation, is rate limiting in the deacidification process

Temperature dependence of carbon isotope fractionation in CAM plants

Energy Technology Data Exchange (ETDEWEB)

Deleens, E.; Treichel, I.; O' Leary, M.H.

1985-09-01

The carbon isotope fractionation associated with nocturnal malic acid synthesis in Kalanchoe daigremontiana and Bryophyllum tubiflorum was calculated from the isotopic composition of carbon-4 of malic acid, after appropriate corrections. In the lowest temperature treatment (17/sup 0/C nights, 23/sup 0/C days), the isotope fractionation for both plants is -4% per thousand (that is, malate is enriched in /sup 13/C relative to the atmosphere). For K. daigremontiana, the isotope fractionation decreases with increasing temperature, becoming approximately 0% per thousand at 27/sup 0/C/33/sup 0/C. Detailed analysis of temperature effects on the isotope fractionation indicates that stomatal aperture decreases with increasing temperature and carboxylation capacity increases. For B. tubiflorum, the temperature dependence of the isotope fractionation is smaller and is principally attributed to the normal temperature dependences of the rates of diffusion and carboxylation steps. The small change in the isotopic composition of remaining malic acid in both species which is observed during deacidification indicates that malate release, rather than decarboxylation, is rate limiting in the deacidification process. 28 references, 1 figure, 4 tables.

On the Sources of Salinity in Groundwater under Plain Areas. Insights from {delta}{sup 18}O, {delta}{sup 2}H and Hydrochemistry in the Azul River Basin, Argentina

Energy Technology Data Exchange (ETDEWEB)

Zabala, M. E.; Varni, M.; Weinzettel, P. [Instituto de Hidrologia de llanuras, Azul (Argentina); Manzano, M. [Technical University of Cartagena (Spain)

2013-07-15

The Azul River basin, with some 6200 km{sup 2}, is located in the plains of Buenos Aires Province, Argentina. The Azul River flows along 160 km from the Tandilia Range, in the SW, to the Channel 11, in the NE. Average annual precipitation is 1005 mm (1988-2000); mean reference evapotranspiration is 1090 mm. The geology consists of Miocene to recent sediments, mostly sands and silts with some clay and calcrete layers, overlying crystalline rocks and marine sediments. The water table is shallow and groundwater in the aquifer upper 30 m displays an increasing salinity from SW to NE. The previous hypothesis to explain the salinity was infiltration of evapo-concentrated surface water, as the small soil slope in the northern basin (< 0.2%) induces rainfall accumulation in lowlands, where water evaporates prior to infiltration. But recent chemical and isotopic data reveal two salinity sources: evaporation of recent recharge water, and mixing with old saline groundwater of yet unknown origin. (author)

δ18O water isotope in the iLOVECLIM model (version 1.0 – Part 1: Implementation and verification

Directory of Open Access Journals (Sweden)

D. M. Roche

2013-09-01

Full Text Available A new 18O stable water isotope scheme is developed for three components of the iLOVECLIM coupled climate model: atmospheric, oceanic and land surface. The equations required to reproduce the fractionation of stable water isotopes in the simplified atmospheric model ECBilt are developed consistently with the moisture scheme. Simplifications in the processes are made to account for the simplified vertical structure including only one moist layer. Implementation of these equations together with a passive tracer scheme for the ocean and a equilibrium fractionation scheme for the land surface leads to the closure of the (isotopic- water budget in our climate system. Following the implementation, verification of the existence of usual δ18O to climatic relationships are performed for the Rayleigh distillation, the Dansgaard relationship and the δ18O –salinity relationship. Advantages and caveats of the approach taken are outlined. The isotopic fields simulated are shown to reproduce most expected oxygen-18–climate relationships with the notable exception of the isotopic composition in Antarctica.

Selective photoionization of gadolinium isotopes with a polarized laser

International Nuclear Information System (INIS)

Le Guyadec, E.

1990-06-01

The aim of this study is the use of gadolinium 157 as burnable poison in nuclear reactors. Spectroscopic isotopic displacements between Gd 156 and Gd 157 are low and the separation method studied is based on differentiated behavior, concerning polarized light, of even and odd gadolinium isotopes coming from their difference of nuclear spin. On this principle is based the simplest photoionization scheme. Selective ionization of odd isotopes is realized from the fundamental state with three resonating photons colinearly polarized. The experimental study confirms the possibility of efficient photoionization. The measured selectivity between Gd 157 and even isotope is over 48 in defined conditions because it can be destroyed by a magnetic field or if photons are not well polarized. Calculations and observations are in good agreement. Odd gadolinium isotope separation is feasible and effects preventing separation are evidenced [fr