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  • Articles: DFG German National Licenses  (3)
  • 1985-1989  (3)
  • 1950-1954
  • 1945-1949
  • 24-hour pH test  (1)
  • Denitrification  (1)
  • Gastroenteritis  (1)
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  • Articles: DFG German National Licenses  (3)
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Years
  • 1985-1989  (3)
  • 1950-1954
  • 1945-1949
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Biology and fertility of soils 8 (1989), S. 219-226 
    ISSN: 1432-0789
    Keywords: Denitrification ; Acetylen inhibition technique ; 15N technique ; Organic residues ; Mineral fertilization ; Irrigation ; Temperate climate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Denitrification N losses can be determined by three methods. The first is by estimating the non-recovery of 15 N-labelled compounds (15N-balance method). Using this method, denitrification losses are deduced from the balance of an N budged (15N-labeled fertilizer), having accounted for transformations in soil, plant uptake, and leaching losses. The evolution of gaseous N from native soil N is not taken into account by this procedure. Studies on arable land with annual crops in the temperate zone have shown that of the fertilizer N applied, about 20–500% (10–70 kg N* ha−1) is not recovered at the end of the growth period. The second method of determining denitrification N losses is by in situ field measurement of 15 N 2 and 15 N 2 O production. Under this procedure, 15N-enriched N is applied to a plot and the denitrification N losses are determined by covering the soil. The method allows a quantitative estimate of the relative contributions to the emitted gas by both the original enriched source and the native soil N. N-evolution rates measured on arable land under a temperate climate are approximately the same order of magnitude as the N losses estimated by the non-recovery of 15 N method. The third measuring procedure is based on the acetylene inhibition phenomenon. This principle uses the inhibition of bacterial N2O reduction to N2 in the presence of acetylene (C2H2). The methoddetermines the denitrification of all NO3 −-N irrespective of its source. Measurements on classical crop production systems show maximum N losses in the temperate climate of about 20–30 kg N* ha−1 during the growth period of annual crops. A similar level of denitrification is estimated for grassland sites under the same climate. In the subtropics (mediterranean climate with hot summers and mild winters), from both intensively cultivated arable land and grassland sites, N losses may exceed 200 kg* ha−1 year−1. Without the use of irrigation the denitrification flux is negligible in spite of the high temperatures in this climate.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1076
    Keywords: Gastroenteritis ; Infants ; Rotavirus ; Adenovirus 31 ; Genome type
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract An an infants' ward, gastroenteritis occurred in five children in two groups, probably by nosocomial spead of adenovirus 31 (three cases) and adenovirus 31 + rotavirus (two cases). The infants recovered well. The DNA of adenovirus 31 isolates was analysed with ten restriction endonucleases and found identical for all five strains, but different from the prototype.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 33 (1988), S. 1127-1133 
    ISSN: 1573-2568
    Keywords: gastroesophageal reflux disease ; esophagitis ; 24-hour pH test ; gastroesophageal reflux tests
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract If 24-hour esophageal pH monitoring is to be a useful diagnostic tool, it must reliably discriminate gastroesophageal reflux patients despite daily variations in distal esophageal acid exposure. To address this issue, we studied 53 subjects (14 healthy normals, 14 esophagitis patients, and 25 patients with atypical symptoms) with two ambulatory pH tests performed within 10 days of each other. Intrasubject reproducibility of 12 pH parameters to discriminate the presence of abnormal acid reflux was determined. As a group, the parameters of percent time with pH〈4 (total, upright, recumbent) were most reproducible (80%). Therefore, a subject was defined as having gastroesophageal reflux disease if at least one of these three values were abnormal. Intrasubject reproducibility for the diagnosis of reflux disease was 89% for the entire sample. Among subsets, the reproducibility was 93% for the normals and esophagitis patients and 84% for the atypical symptom patients. Total percent time with pH〈4 was the single most discriminate pH parameter (85%) and nearly equaled that of the three combined parameters (89%). The intrasubject variability of this parameter was determined by the mean ±2sd of the relative differences between the two test results for all 53 subjects. Total percent time with pH〈4 may vary between tests by a factor of 3.2-fold or less (218% higher to 69% lower). We conclude: (1) ambulatory 24-hr esophageal monitoring is a reproducible test for the diagnosis of gastroesophageal reflux disease; and (2) the large intrastudy variability in 24-hr total acid exposure may limit this test's usefulness as a measurement of therapeutic improvement.
    Type of Medium: Electronic Resource
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