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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 26 (1978), S. 3-5 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physics of the Earth and Planetary Interiors 85 (1994), S. 181-193 
    ISSN: 0031-9201
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1365-3091
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Geosciences
    Notes: A small, closed, lacustrine system developed during the restraining overstep stages of the Oligocene As Pontes strike-slip basin (Spain). The increase in basin accommodation and the headward spread of the drainage, which increased the water input, triggered a change from shallow, holomictic to deeper, meromictic conditions. The lower, shallow, lacustrine assemblage consists of mudstone–carbonate cycles recording lacustrine–palustrine ramp deposition in a saline lake. High Sr content in some early diagenetic calcites suggests that aragonite and calcite made up the primary carbonate muds. Early dolomitization took place together with widespread pedogenic activity. The upper, deep, freshwater, lacustrine assemblage includes bundles of carbonate–clay rhythmites and fine-grained turbidite beds. Primary calcite and diagenetic siderite make up the carbonate laminae. The Mg content of the primary carbonates records variations in Mg/Ca ratios in lacustrine waters. δ18O and δ13C covariance trends in calcite reinforce closed drainage conditions. δ18O data indicate that the lake system changed rapidly from short-lived isotopically light periods (i.e. from seasonal to pluriannual) to longer steady-state periods of heavier δ18O (i.e. from pluriannual to millennial). The small δ13C changes in the covariant trends were caused by dilute inflow, changing the contributions of dissolved organic carbon in the system and/or internal variations in lacustrine organic productivity and recycling. In both shallow and deep carbonate facies, sulphate reduction and methanogenesis may account, respectively, for the larger negative and positive δ13C shifts recorded in the early diagenetic carbonates (calcite, dolomite and siderite). The lacustrine system was very susceptible to high-frequency, climatically forced water balance variations. These climatic oscillations interfered with the low-frequency tectonic and morphological changes in the basin catchment. This resulted in the superposition of high-order depositional, mineralogical and geochemical cycles and rhythms on the lower order lacustrine infill sequence.
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Physics and Chemistry of Solids 51 (1990), S. 165-170 
    ISSN: 0022-3697
    Keywords: Oxygen ; cyclic voltametry ; diffusion ; fast conductor ; ionic conductor
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics Letters 81 (1981), S. 402-405 
    ISSN: 0009-2614
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 195 (1995), S. 91-95 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The method described in a previous work to separate trace amounts of selenium in organic samples without using a carrier, based on the adsorption on active carbon filters of the complex formed with ammonium pyrrolidindithiocarbamate (APDC) at pH 1.5–2, has been applied to urine samples from 15 females patients suffering from cervical uterine cancer. With this type of sample the method reaches a maximum sensitivity (few ppb) with a good statistical variation (±12%). Since the highest concentration of selenium in human tissues is found in the kidney, and the elimination of this element is mainly by the urine, the method seems to be a powerful tool in the research about the human metabolism of selenium. This paper shows a possible relation of selenium concentration in human urine and the evolution time of cervical uterine cancer, in spite of limits imposed by the statistical error plus the inhomogeneity of the sample.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 193 (1995), S. 259-268 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Gamma exposure rate and radon levels were measured in 75 single-family dwellings in Mexico City in order to correlate them with local environment. Radon monitoring was performed both indoors and outdoors using a continuous working level monitor for short-lived radon decay products; the gamma exposure rate was measured using CaSO4: Dy+PTFE. The results obtained show a log-normal distribution. The mean indoor radon concentration is lower than 45 Bq/m3 and the mean indoor gamma exposure rate was 11.29 μR/h.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract A method is described to separate trace amounts of selenium in organic samples without using a carrier, based on the adsorption on active carbon filters of the complex formed with APDC at pH 1.5. The separation is made prior to the neutron irradiation and the correction for selenium in the reagents performed by the irradiation of a blank. The method has been successfully used in fodder samples as well as some other organic reference materials, using a fast pneumatic transfersystem, which takes the samples from the irradiation position to the counting position in 3s, with the only limitation of the thermal neutron flux available, 4.7·1011 cm−2·s−1. Detection limits of 0.1 μg are obtained under these experimental conditions.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 145 (1990), S. 445-452 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract A method is described to separate trace amounts of selenium in biological samples without using a carrier. This method is based on the adsorption on active carbon of the complex ion formed with APDC /ammonium salt of l-pyrrolidine carbodithioic acid/ at pH 1. The efficiency of the radiochemical separation described is measured by using carrier-free75Se labelled solutions of sodium selenite at selenium concentrations from 3.5×10−8 to 3.5×10−11 g ml−1. The results were between 95% and 98% with statistical variations from 2% to 10%. The determination of selenium can be made following this separation either through75Se in the traditional way, or through77mSe if the separation is performed prior to irradiation. The detection limits on the available conditions were 0.01 ppm for75Se and 0.1 ppm for77mSe. When the analysis is performed through75Se /t=120 d/, the statistical error is notably smaller because the counting time may be considerable, whereas through77mSe/t=17.5 s/it is higher than 20%, depending on the concentration and the available neutron flux. However, the advantages of gaining time and the fact of performing the trace separation from a non radioactive material, make both procedures competitive as useful tools for the research on the function of Se in vertebrates.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 192 (1995), S. 97-100 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract Mass Spectrometry has been the usual method to determine Ar concentrations in mineral samples for dating them through the40Ar/40K ratio. This technique has been replaced since 1966 by measurement of40Ar/39Ar ratio, after artificial production of39Ar from the39K(n,p)39Ar reaction produced in the fast neutron flux of a nuclear reactor. This method requires the fusion of the sample by incremental heating until reaching a temperature of 1000°C in order to get the total release of both argon isotopes. In principle, it should be possible to determine the40Ar/40K ratio by activation analysis in an easier, non-destructive way, but it presents the following drawbacks: manufacture of argon standards; usual low ratio peak/Compton distribution for both peaks: 1.29 Mev and 1.52 Mev (41Ar and42K respectively), since potassium minerals are usually very rich in sodium, manganese and chlorine; reaction41K(n,p)41Ar induced by fast neutrons present in the thermal flux; and possible contamination of the samples and standards with atmospheric40Ar (99.6% of elementary Ar, whose proportion in the atmosphere at sea level is 0.93%). This paper describes how these problems may be solved, also determining the limits of Ar and K concentration related to Compton distribution, in our experimental conditions.
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