In 2006, soils were collected to a depth of 3.3 m from 4 locations at two sites south of
Soils were air-dried and passed through a 2-mm sieve, then analyzed for NO3-N using 2M KCl and P using a modified sequential P extraction procedure, determining concentrations of: 1) water soluble; 2) soluble and loosely bound; 3) Al-bound; 4) Fe-bound; 5) occluded (i.e. Fe coated); and 6) Ca bound P. Nitrate-N concentrations were lower than expected, potentially due to leaching, plant utilization, or denitrification. The majority of P at both sites was bound to the Ca phase, likely due to parent mineralogy. Differences existed at both sites for pH, but the overriding factor affecting P forms was likely redox. Reduced conditions caused the dissolution of ferric-bearing P mineral phases and the subsequent re-precipitation of Al- and Ca-bound P phases. Overall, systems have been successful at immobilizing P and appear to have an extended life expectancy.