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  • 1
    Publication Date: 2023-01-14
    Keywords: DATE/TIME; DEPTH, water; Ehhalt1969; Latitude of event; Longitude of event; OCE; Oceanography; δ Deuterium
    Type: Dataset
    Format: text/tab-separated-values, 14 data points
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 209 (1966), S. 903-904 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] In view of the time of onset and the brief duration of the tritium peak it seems far more likely that the tritiated hydrogen was released during the reactor accident at Windscale on October 10 and 11, 1957. Since the samples were taken two days apart, the initial rise in Fig. 1 is not well defined, ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 1 (1983), S. 27-51 
    ISSN: 1573-0662
    Keywords: Variance ; trace/gases ; stratosphere ; mixing length ; mixing surfaces
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The relative variances in stratospheric observations of longlived trace gases CH4, N2O, CF2Cl2, CFCl3 show large differences. These differences are greatly reduced when the local mean standard deviation is normalized to the local vertical gradient. This ratio, called ‘equivalent displacement height’ exhibits a characteristic vertical profile which is very similar for all the longlived trace gases, as well as for O3. With the help of this ratio, it is demonstrated that the variances are essentially due to natural causes, i.e., transport. Using the mixing length hypothesis a theoretical expression for the equivalent displacement height is derived. From it the meridional slope of the mixing surfaces and the mixing length can be calculated as function of the altitude. Additional information is obtained on the variance of that slope. The uncertainty of the measured mean trace gas profiles is defined.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 2 (1984), S. 117-124 
    ISSN: 1573-0662
    Keywords: Acetylene ; stratospheric profiles ; trace gas measurements ; stratosphere-troposphere exchange
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Stratospheric measurements of acetylene up to altitudes of 30 km are presented. The air samples were collected during three different balloon flights, two of them at 44°N, one at 32°N using balloon borne, liquid neon-cooled, cryosamplers. Their acetylene concentration was measured in the laboratory by flame ionisation gaschromatography. The different profiles at 32°N and 44°N are discussed with respect to possible vertical exchange processes and compared with published model calculations.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 2 (1984), S. 191-202 
    ISSN: 1573-0662
    Keywords: Stratospheric photochemistry ; HO2 -, NO2 +in situ data ; vertical profiles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Vertical profiles of stratospheric HO2 and NO2 concentrations were determined using matrix isolation and ESR. Up to 10 different samples per flight were collected in situ by a balloon borne cryosampler. Free radicals and trace constituents which are condensable at 68 K are trapped in a polycristalline H2O or D2O matrix. After collection, the samples are stored at a temperature below 83 K until they are analysed in the laboratory by X-band ESR spectroscopy at 4 K. The HO2 and NO2 were identified and calibrated by comparison with standard samples collected in the laboratory under typical stratospheric sampling conditions. From several flights over Southern France (44°N) we obtained two profiles of the stratospheric NO2 mixing ratio. One, from 21 October 1982, agrees well with previous measurements. The other, from 8 October 1981, is lower by one order of magnitude. The few HO2 data obtained around 35 km altitude agree with previous measurements. An isolated measurement at 17 km altitude is one order of magnitude higher than the model predicted HO2 concentration.
    Type of Medium: Electronic Resource
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