“…The results are in accordance with the findings of Giordano and Mortvedt (1973) and Das, Karak, and Karmakar (2002). The amount of applied Zn recovered was less due to application of ZnSO 4 than to Zn-EDTA, which may be attributed to rapid dissociation of Zn +2 from ZnSO 4 and subsequent precipitation of Zn as ZnCO 3 and hydrated zinc carbonate [Zn 3 (CO 3 ) 2 (OH) 2 ] or hydroxide and carbonate (Kalbasi, Racz, and Lewen Rudgers 1978) At Z29 stage (Figures 1, 2, and 3), the greatest 0.1 N HCl, DTPA, and 0.05 N HCl-extractable Zn concentrations were 11.63, 6.79, and 4.62 mg kg 21 , respectively, in the treatment T 7 (1.0 kg Zn ha 21 as Zn-EDTA at basal) and recorded 37.5, 27.6, and 17.8% increases over their split application (T 8 ). Similarly, the basal applications of 10 and 20 kg Zn ha 21 as ZnSO 4 (T 2 and T 4 ) resulted in 7 and 23.6% increase in 0.1 N HCl, 53.1 and 12.6% increase in DTPA, and 58.6 and 17% increase in 0.05 N HCl over split applications (T 3 and T 5 ), respectively, at Z29 stage.…”