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ABSTRACT
The Mn labile pool was determined in a wide range of United Kingdom soils, using 54Mn tracer and two different extractants, CaCl2 and DTPA. Good agreement was obtained between E values obtained by two different equilibration procedures in CaCl2, but for most soils the concentrations of CaCl2-extractable Mn were considerably lower than the E-values. Higher E-values were obtained in DTPA than in CaCl2, indicating that the former dissolved some nonisotopically exchangeable Mn. The rate of disappearance of 54Mn from the soil solution, and its distribution in various fractions, differed greatly between the soils. Generally, the radioisotope labeled all the soil fractions determined, with the majority of 54Mn associated with the water-soluble + exchangeable, organically bound and easily reducible oxide fractions. When the labeled soils were subjected to air and oven-drying, net gains of 54Mn were observed in the water-soluble + exchangeable, resistant and residual Mn fractions, with corresponding reductions in the easily reducible oxide fractions. Upon drying, native Mn increased in the water-soluble + exchangeable and EDTA-extractable fractions. Possible mechanisms for these changes are discussed.
1 Contribution from The Edinburgh School of Agriculture, West Mains Road, Edinburgh, EH9 3JG, Scotland, UK.
2 Former Postgraduate Student, and Head of Soil Science Dept., respectively. Present address of senior author is Agency of Environmental Conservation, Heritage 2 Office Bldg., 79 River Street, Montpelier, VT 05602.
Received for publication September 8, 1983. Accepted for publication November 2, 1983.
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