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  • Artikel: DFG Deutsche Nationallizenzen  (5)
  • Neurone number  (3)
  • ammonium sulfate  (2)
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  • Artikel: DFG Deutsche Nationallizenzen  (5)
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Erscheinungszeitraum
  • 1
    ISSN: 1573-0867
    Schlagwort(e): 1-amidino-2-thiourea ; 3,5-diamino-1,2,4-thiadiazole ; dicyandiamide ; thiourea ; nitrification inhibitor ; urea ; ammonium sulfate ; Nitrosomonas europaea ; N-fertilizer
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft
    Notizen: Abstract The degradation of guanylthiourea (GTU) via 3,5-diamino-1,2,4-thiadiazole (TDZ) to dicyandiamide (DCD) was studied in selected soils. All three compounds could be determined by HPLC. GTU decomposed rapidly (within hours-days), the reaction from TDZ to DCD continued more slowly (within days-weeks). Soil type and temperature had an essential effect on the rate of degradation; conspicuous was a more rapid breakdown of GTU in presence of ammonium sulfate (AS) than in combination with urea. Each compound is a nitrification inhibitor; inNitrosomonas cell suspensions, 0.5 ppm GTU and 10 ppm TDZ achieved an effect comparable to 200 ppm DCD. The combination of these two effects—degradation in soil and inhibition of nitrification—were studied in soil incubation experiments. The three substances had inhibitory effects also in soil, however at significantly different application rates (20 ppm GTU or TDZ and 30 ppm DCD). Using these concentrations, AS/DCD and urea/GTU showed similar effects. Urea/GTU retarded nitrification by the factor 1.7 as compared to urea/DCD. AS/GTU had no advantage over AS/DCD which can be explained by the more rapid degradation of GTU in presence of AS. Urea/GTU apparently presents a promising possibility to utilize N-fertilizers more efficiently.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1432-0533
    Schlagwort(e): Key words Huntington's disease ; Human cerebral cortex ; Striatum ; Neurone number ; Stereology
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The total cortical and striatal neurone and glial numbers were estimated in five cases of Huntington's disease (three males, two females) and five age- and sex-matched control cases. Serial 500-μm-thick gallocyanin-stained frontal sections through the left hemisphere were analysed using Cavalieri's principle for volume and the optical disector for cell density estimations. The average cortical neurone number of five controls (mean age 53±13 years, range 36 – 72 years) was 5.97×109±320×106, the average number of small striatal neurones was 82×106±15.8×106. The left striatum (caudatum, putamen, and accumbens) contained a mean of 273×106±53×106 glial cells (oligodendrocytes, astrocytes and unclassifiable glial profiles). The mean cortical neurone number in Huntington's disease patients (mean age 49±14 years, range 36 – 75 years) was diminished by about 33  % to 3.99×109±218×106 nerve cells (P≤ 0.012, Mann-Whitney U-test). The mean number of small striatal neurones decreased tremendously to 9.72 × 106± 3.64×106 ( – 88  %). The decrease in total glial cells was less pronounced (193 × 106±26 × 106) but the mean glial index, the numerical ratio of glial cells per neurone, increased from 3.35 to 22.59 in Huntington's disease. Qualitatively, neuronal loss was most pronounced in supragranular layers of primary sensory areas (Brodmann's areae 3,1,2; area 17, area 41). Layer IIIc pyramidal cells were preferentially lost in association areas of the temporal, frontal, and parietal lobes, whereas spared layer IV granule cells formed a conspicuous band between layer III and V in these fields. Methodological issues are discussed in context with previous investigations and similarities and differences of laminar and lobar nerve cell loss in Huntington's disease are compared with nerve cell degeneration in other neuropsychiatric diseases.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    ISSN: 1432-0533
    Schlagwort(e): Huntington's disease ; Human cerebral cortex ; Striatum ; Neurone number ; Stereology
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The total cortical and striatal neurone and glial numbers were estimated in five cases of Huntington's disease (three males, two females) and five age-and sex-matched control cases. Serial 500-μm-thick gallocyanin-stained frontal sections through the left hemisphere were analysed using Cavalieri's principle for volume and the optical disector for cell density estimations. The average cortical neurone number of five controls (mean age 53±13 years, range 36–72 years) was 5.97×109±320×106, the average number of small striatal neurones was 82×106±15.8×106. The left striatum (caudatum, putamen, and accumbens) contained a mean of 273×106±53×106 glial cells (oligodendrocytes, astrocytes and unclassifiable glial profiles). The mean cortical neurone number in Huntington's disease patients (mean age 49±14 years, range 36–75 years) was diminished by about 33% to 3.99×109±218×106 nerve cells (P≦0.012, Mann-Whitney U-test). The mean number of small striatal neurones decreased tremendously to 9.72×106±3.64×106 (−88%). The decrease in total glial cells was less pronounced (193×106±26×106) but the mean glial index, the numerical ratio of glial cells per neurone, increased from 3.35 to 22.59 in Huntington's disease. Qualitatively, neuronal loss was most pronounced in supragranular layers of primary sensory areas (Brodmann's areae 3,1,2; area 17, area 41). Layer IIIc pyramidal cells were preferentially lost in association areas of the temporal, frontal, and parietal lobes, whereas spared layer IV granule cells formed a conspicuous band between layer III and V in these fields. Methodological issues are discussed in context with previous investigations and similarities and differences of laminar and lobar nerve cell loss in Huntington's disease are compared with nerve cell degeneration in other neuropsychiatric diseases.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    ISSN: 1432-0533
    Schlagwort(e): Key words Huntington's disease ; Human brain ; Thalamus ; Nuclei centromedianus-parafascicularis ; Neurone number
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract The centromedian-parafascicular complex represents a nodal point in the neuronal loop comprising striatum – globulus pallidus – thalamus – striatum. Striatal neurone degeneration is a hallmark in Huntington's disease and we were interested in estimating total neurone and glial number in this thalamic nuclear complex. Serial 500-μm-thick gallocyanin-stained frontal sections of the left hemisphere from six cases of Huntington's disease patients (three females, three males) and six age- and sex-matched controls were investigated applying Cavalieri's principle and the optical disector. Mean neurone number in the controls was 646,952 ± 129,668 cells versus 291,763 ± 60,122 in Huntington's disease patients (Mann-Whitney U-test, P 〈 0.001). Total glial cell number (astrocytes, oligodendrocytes, microglia, and unclassifiable glial profiles) was higher in controls with 9,544,191 ± 3,028,944 versus 6,961,989 ± 2,241,543 in Huntington's disease patients (Mann-Whitney U-test, P 〈 0.021). Considerable increase of fibrous astroglia within the centromedian-parafascicular complex could be observed after Gallyas' impregnation. Most probably this cell type enhanced the numerical ratio between glial number and neurone number (glial index: Huntington's disease patients = 24.4 ± 8.1; controls = 15.0 ± 5.2; Mann-Whitney U-test, P 〈 0.013). The neurone number in the centromedian-parafascicular complex correlated negatively, although statistically not significantly, with the striatal neurone number. This lack of correlation between an 80% neuronal loss in the striatum and a 55% neurone loss in the centromedian-parafascicular complex points to viable neuronal circuits connecting the centromedian-parafascicular complex with cortical and subcortical regions that are less affected in Huntington's disease.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Nutrient cycling in agroecosystems 21 (1990), S. 179-183 
    ISSN: 1573-0867
    Schlagwort(e): 1-amidino-2-thiourea ; dicyandiamide ; nitrification inhibitor ; urea ; ammonium sulfate ; N-fertilizer ; nitrate leaching
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft
    Notizen: Abstract The efficiency of the nitrification inhibitors dicyandiamide (DCD) and 1-amidino-2-thiourea (or guanylthiourea = GTU) in reducing losses from N fertilizers was investigated in two greenhouse experiments where leaching of nitrate-N was induced by percolation at 3 and 5 weeks after fertilization. At an application rate of 10% by weight of fertilizer-N (e.g. 10 kg GTU/ha), GTU in combination with ammonium sulfate (AS) had effects similar to those of DCD (e.g. 15 kg DCD/ha) with regard to nitrate leaching, plant yields and nitrogen uptake. However, in combination with urea (U), GTU was more effective than DCD when applied at the same ratio except with a humic sandy clay soil (pH 7.3, 4.4% organic C), where GTU did not perform as effectively. Nitrate leaching was reduced by as much as 50% using U/GTU instead of U/DCD, and plant yield increased by 30%. At temperatures between 17 and 25°C, the combination U/GTU could protect a high percentage of the nitrogen from being nitrified and leached over a 3 to 5 weeks period. The superiority of GTU over DCD was demonstrated especially in the treatments with 5 weeks of preincubation, despite the considerably lower application rate.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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