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  • 2000-2004  (1)
  • 1995-1999  (1)
  • 1935-1939
  • Dorsal root ganglion neurons Gene gun Green fluorescent protein Hippocampal neurons Particle-mediated gene transfer Primary tissue culture Transfection  (1)
  • Nitrogen  (1)
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  • 2000-2004  (1)
  • 1995-1999  (1)
  • 1935-1939
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  • 1
    Electronic Resource
    Electronic Resource
    Effect of nitrogen fertiliser on temporal and spatial variation of mineral nitrogen and microbial biomass in a silvopastoral system (1995)
    Springer
    Biology and fertility of soils 19 (1995), S. 177-185 
    Details
    ISSN: 1432-0789
    Keywords: Excreta ; Fertiliser ; Microbial biomass ; Nitrogen ; Silvopastoral
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Geosciences , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract This paper describes a field study to assess the effect of increasing the frequency of split applications of N fertiliser on the pattern of plant uptake, soil N availability, and microbial biomass C and N. Measurements were taken during the growing season in different positions relative to young trees (Prunus avium L.) in an upland silvopastoral system in its first year after establishment. At fertiliser rates of 72 and 144 kg ha-1 N applied as NH4NO3, increasing the number of split applications increased N uptake by the pasture. Mineral forms of soil N measured 2 weeks after application indicated that residual NH inf4 sup+ -N and total mineral N were also greater in this treatment on certain dates. Soil NO inf3 sup- -N was positively correlated with the soil moisture content, and nitrification reached a maximum in early May and declined rapidly thereafter except within the herbicide-treated areas around the trees where soil moisture had been conserved. Results of the study suggest that high NO inf3 sup- -N in herbicide-treated areas was probably caused by mineralisation of grass residues and low uptake by the tree rather than by preferential urine excretion by sheep sheltering beside the trees. Mean microbial biomass C and N values of 894 and 213 kg ha-1, respectively, were obtained. Microbial C was slightly increased by the higher frequency of split applications at 144 kg ha-1 N and was probably related to the greater herbage production with this treatment. Microbial N was not significantly affected by the N treatments. Both microbial biomass C and N increased during the growing season, resulting in the net immobilisation of at least 45 kg ha-1 N which was later released during the autumn.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00336156
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Particle-mediated gene transfer to rat neurons in primary culture (2000)
    Springer
    Pflügers Archiv 439 (2000), S. 730-738 
    Details
    ISSN: 1432-2013
    Keywords: Dorsal root ganglion neurons Gene gun Green fluorescent protein Hippocampal neurons Particle-mediated gene transfer Primary tissue culture Transfection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Gene transfer into neuronal cells provides an important approach to study their function. Particle-mediated gene delivery was used to transfect rat dorsal root ganglion (DRG) and hippocampal neurons in primary culture with the genes for the enhanced blue and green fluorescent proteins (EBFP and EGFP) under control of the cytomegalovirus promoter. Quantitative analysis of marker protein fluorescence detected expression at 3 h that continued to increase for 48 h. For DRG neurons the optimal expression efficiency of 8±2% was obtained 24 h following transfection. In contrast, approximately 2±1% of hippocampal neurons in culture expressed EGFP at 3 h which subsequently declined. Co-transfection of DRG cultures with two plasmids produced reliable expression of both genes. Transfected DRG neurons exhibited normal electrophysiological properties, and resting and stimulated intracellular Ca2+ concentrations were unchanged. After transfection, 44% of hippocampal neurons remained in functional synaptic networks as indicated by glutamatergic Ca2+ spiking activity. Particle-mediated gene delivery provided a straightforward, reproducible and efficient method for transfection of neurons in primary culture. Transfected cells were easily identified by EGFP fluorescence, enabling subsequent physiological analysis. Biolistic particle bombardment was well tolerated by peripheral neurons, although caution was required when this method was applied to CNS cultures.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s004249900240
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    Paper (German National Licenses)
    Fulltext
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