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  • 1
    ISSN: 1572-9680
    Keywords: Acacia nilotica ; calcareous soils ; Dalbergia sissoo ; re-forestation ; salinity control ; water use efficiency
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Appropriate tree species and planting methods can help rehabilitation of arid areas — that are characterized by low rainfall, high evapotranspiration demands, highly saline ground waters and calcareous subsoils. The growth of Acacia nilotica and Dalbergia sissoo saplings planted in irrigation furrows in such an arid zone of northwest India was not affected adversely by irrigation with saline water of EC W 10.5 dS m−1. The growth of A. nilotica, measured in terms of sapling survival, plant height and biomass yields, was better than that of D. sissoo. Increasing the period of irrigation from the recommended practice of irrigating only in the first year dry season (October–June) to second and third dry seasons (years) improved the sapling survival, growth and biomass (two-to-three-fold) and water use efficiency (two-to-four fold). Most of the salts added with saline irrigation were accumulated below the irrigation channels and were pushed laterally during the monsoon season. The results indicate that the furrow planting technique could be adopted as an afforestation practice in view of the creation of favourable water and salt regimes and their impact on the establishment of trees saplings. Irrigation water supplies for a minimum of intitially two years after transplanting seemed necessary.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0749-1581
    Keywords: steroids ; 1H NMR ; 13C NMR ; coupling constants ; conformational analysis ; 1D TOCSY ; NOE ; cyclosteroids ; cyclopropanosteroids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Proton and carbon NMR data are provided for 21 ring A and ring B cyclosteroids and cyclopropano (or methylene) steroids. Shift assignments were made using standard 2D NMR techniques, while ring A proton subspectra were extracted with a 1D TOCSY experiment. Coupling constants were obtained from iterative spin system simulation of these sub-spectra. Ring A conformations were determined from the two- and three-bond proton-proton couplings and NOE measurements. The utility and limitations of extended Karplus-type equations, the effect of cyclopropyl groups on vicinal and geminal couplings and cyclopropane-induced chemical shifts are discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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