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ABSTRACT
The same amount of P in 0.01M CaCl2 was repeatedly added to 12 soils to measure the P sorption of the soils. Compared with the P sorption maximum calculated from the Langmuir equation, repeated additions showed about twice as much sorption. However, the two measurements were well correlated. At low P concentration or in soils with low sorption capacity, each addition showed about the same sorption increment after the first three to four additions. Between 6 and 35% of the amount sorbed after 10 additions of P was desorbed in 10 subsequent additions of 0.01M CaCl2. The P sorption was lower at 4°C than at room temperature. The only soil parameter that significantly influenced the sorption capacity with dithionite—citrate extractable Al. The sorption capacity measured by repeated additions of a solution of the same P concentration as wastewater seems to give a better estimate of the field sorption capacity than the Langmuir sorption maximum.
Key Words: desorption isotherms extractable Fe and Al particle-size distribution cation exchange capacity pH Langmuir equation
1 Contribution of the Norwegian Forest Res. Inst., P.O. Box 61, N-1432 Aas-NLH, Norway. Funded in part by the Agric. Res. Council of Norway.
2 Soil Scientist, Norwegian Forest Res. Inst.
Received for publication March 3, 1983.
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