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  • 1
    ISSN: 1573-0867
    Schlagwort(e): Liming ; B nutrition ; pea ; corn ; hot-water soluble B ; soil pH ; acid Alfisol
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Land- und Forstwirtschaft, Gartenbau, Fischereiwirtschaft, Hauswirtschaft
    Notizen: Abstract A field experiment was conducted during 1986–87 on a sandy loam acid Alfisol of Barapani, Meghalaya, India to study the effect of liming on boron nutrition of pea and corn grown in a sequence. Lime and boron were applied to pea and their residual effect was studied on corn. Application of 1.5 kg B ha−1 significantly increased the pod and stover yield of pea. A sharp yield depression occurred at higher B rates. Liming accentuated B deficiency in the absence of B treatment and it cured toxicity arising from excess B supply. A combination of B at 1.5 kg ha−1 and lime at 3.0 t ha−1 was optimum for pea, but this level of B application was insufficient to meet B requirements of succeeding corn. With higher rates of B fertilization, the residual effect of B on corn yield was significant. Concentration of B in shoot, pod, grain and stover of crops increased with the rate of B application. With increasing liming rate, B concentration decreased. Addition of B increased the hot-water soluble B in soil. The availability of native and added B decreased sharply with increasing liming rate.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 1165-1171 
    ISSN: 0360-6376
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The Kelen-Tüdös linear graphical method was used to determine the copolymerization parameters of some halogen-substituted (e.g., Cl, Br, I) aniline monomers. It was found during copolymerization with p-aminobenzoic acid or p-aminophenol that the reactivity of these monomers followed the order of their basic strength. The order of their basic strength. The order of their reactivity, however, was reversed if they copolymerized with sulfanilic acid (SA). This reversal has been interpreted in terms of the resonance stabilization of monomers, the nature of the acidic functional groups present in the comonomer, and the influence of electron-accepting or electron-donating groups present in the comonomers.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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