Reclamation of Alkali Soils: Influence of Amendments and Leaching on Transformation and Availability of Phosphorus

Abstract

Phosphorus (P) availability to plants in reclaimed alkali soils was the main objective of this study, which was also focused on P transformations, decrease in Olsen‐P content, and magnitude of P lost in leachate in course of amendment application and leaching. Liquid sodium bicarbonate (NaHCO₃) was added to nonalkali soils to set up four ESP (exchangeable sodium percentage) levels (viz., 2.9, 25.0, 50.0, and 75.0), but actual ESP levels obtained were 2.9, 24.6, 51.2, and 75.3. Amendments (viz., gypsum and pyrites) and P treatments (viz., 0 and 50 mg P Kg^?1) were mixed with dry, sieved soil before filling into PVC (polyvinyl chloride) drainage columns, which were then compacted to uniform bulk density and leached with deionized water for 30 days. Results indicated that the pH and electrical conductivity (EC) of the soils increased with increase in ESP level of the soil but decreased with amendment application. Phosphorus addition to alkali soils decreased the pH on day 30, but it could not affect the EC of the soils. Successive increase in the ESP level of the soil increased the pH and EC off the leachate. Gypsum‐amended soils exhibited lower pH and EC values than pyrite‐amended soils. The EC of the leachate decreased sharply with time in amended soils, but the pH decreased slowly. Phosphorus addition affected the leachate pH earlier than the soil pH. Cumulative volume of leachate decreased with increasing ESP levels, but it increased with amendment and phosphorus application. Leaching of P increased with increase in ESP levels, and the maximum cumulative loss of P was 11.2 mg Kg^?1 in the 75.3 ESP soil. Cumulative P lost in the pyrite‐amended soils was higher than the gypsum‐amended soils. Phosphorus leaching in the gypsum‐amended soils stopped at day 10 and beyond, but it continued until day 30 in the pyrite‐amended soils. Part of the applied P in alkali soils was also lost along with the native P, whereas it was protected in the nonalkali soils. OlsenP increased with increasing ESP levels, and alkali soils invariably contained higher Olsen P than nonalkali soils. At day 30, alkali soils contained much higher Olsen P (12.6 mg Kg^?1) than nonalkali soils (5.9 mg Kg^?1). In general, there was a decrease in the Olsen P with both of the amendments, but it decreased more with pyrites than with gypsum. Phosphorus added through monopotassium phosphate (KH₂PO₄) remained extractable by Olsen's extractant up to day 30. Results also indicated that percent distribution of ammonium chloride (NH₄Cl)‐P, calcium (Ca)‐P, and unknown P increased with rising ESP levels but iron (Fe)‐aluminum (Al)‐bound P and residual P decreased. Percent distribution of Ca‐P and unknown P exhibited an increase with time also. Unamended alkali soils contained more NH₄Cl‐P than amended ones. Iron and Al‐ bound P and residual P increased more with pyrites, whereas formation of Ca‐P and unknown P was enhanced with gypsum. Applied P tended to convert more into NH₄Cl‐P, Ca‐P, and residual P than to Fe‐Al‐bound P or unknown P fractions. Models developed to estimate Olsen P and P concentration in leachate, through pH or EC, have application value for P management in alkali soils that are leached after application of amendments.