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Title: Solubility characteristics of residual phosphate in a fertilized and limed ultisol

Journal Article · · Soil Sci. Soc. Am. J.; (United States)
OSTI ID:6065514

Except at very low P rates, residual soil P (i.e., that measured by most extraction methods) continues to increase with annual additions of P fertilizer. Phosphorus retention mechanisms, however, are still much debated and difficult to prove or disprove. In an effort to determine whether the solubility of phosphate minerals controlled soil-solution P concentration in the field under some conditions, samples of a Benndale sandy loam were collected from plots of a field experiment with different pH and P levels and analyzed in the laboratory. Several soil pH levels were first established (5.0-8.0); this was followed by annual additions for 7 yr of concentrated superphosphate at five rates varying from 0 to 392 kg P ha/sup -1/ yr/sup -1/ and cropping annually. Soil-solution composition was determined in samples taken 1, 3, and 5 yr after discontinuing P fertilization. Except for the no P treatment, solution P increased with increasing pH up to pH 5.8, then it decreased as pH increased, suggesting the accumulation of a basic phosphate mineral such as hydroxyapatite at about pH 5.8 and above. However, this was not matched by the ion activity product (IAP) for Ca/sub 5/OH(PO/sub 4/)/sub 3/ or any other P mineral. Thus, IAP's could not be used to predict that solid-phase minerals were or were not controlling solution P. Sequential equilibration of selected soil samples with 0.01 M MgCl/sub 2/, however, provided data that strongly supports the hypothesis that hydroxyapatite was present in a high P, high pH soil but not in a low P, high pH or a high P, low pH soil.

Research Organization:
Auburn Univ., AL
DOE Contract Number:
AC05-84OR21400
OSTI ID:
6065514
Journal Information:
Soil Sci. Soc. Am. J.; (United States), Vol. 51:4
Country of Publication:
United States
Language:
English