Autor: |
Varinderpal-Singh, N.S. Dhillon, Raj-Kumar, B.S. Brar |
Zdroj: |
Nutrient Cycling in Agroecosystems; Sep2006, Vol. 76 Issue 1, p29-37, 9p |
Abstrakt: |
Abstract Phosphorus availability from residual P sources in soil is virtually the chemistry of metastable P compounds, i.e., their solubility and interaction with other soil and plant components. Identification of these compounds in soils under long-term application of fertilizers and farmyard manure is unstated and is prerequisite to comprehend the processes of P transformations and cycling in soil-plant system. X-ray diffraction analysis of surface and subsurface soils fertilized for 32 years under a maize–wheat–cowpea (fodder) cropping sequence revealed that P reaction products in soil depends upon the kind of fertilizer added to the soil as well as on management practices. Precipitation of applied P occurred mainly as octa-calcium phosphate, hydroxy apatite and variscite. In addition to these compounds, precipitation as $$\hbox{CaNH}_{4}\hbox{PO}_{4}\cdot\hbox{H}_{2}\hbox{O}$$ was also observed in soil receiving diammonium phosphate rather than super phosphate as a fertilizer P source. Continuous application of farmyard manure (FYM) for three decades inhibited the conversion of applied P to more stable forms such as variscite and hydroxy apatite. The different P reaction products govern the availability of residual soil-P to growing plants. The reaction products formed were associated only with the sand and silt fraction of soil. Phosphorus in the clay fraction is mainly P adsorbed on exchange complexes or entrapped in lattice of silicate minerals. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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