Phosphorus desorption and isotope exchange kinetics in agricultural soils

To improve phosphorus (P) fertilization and environmental assessments, a better understanding of release kinetics of solid-phase P to soil solution is needed. In this study, Fe (hydr)oxide-coated filter papers (Fh papers), isotopic exchange kinetics (IEK) and chemical extractions were used to assess the sizes of fast and slowly desorbing P pools in the soils of six long-term Swedish field experiments. The P desorption data from the Fh-paper extraction of soil (20 days of continual P removal) were fitted with the Lookman two-compartment desorption model, which estimates the pools of fast (Q₁) and slowly (Q₂) desorbing P, and their desorption rates k₁ and k₂. The amounts of isotope-exchangeable P (E) were calculated (E_1min to E_{>3 months}) and compared with Q₁ and Q₂. The strongest relationship was found between E_{1 min} and Q₁ (r² = .87, p < .01). There was also an inverse relationship between the IEK parameter n (the rate of exchange) and k₁ (r² = .52, p < .01) and k₂ (r² = .52, p < .01), suggesting that a soil with a high value of n desorbs less P per time unit. The relationships between these results show that they deliver similar information, but both methods are hard to implement in routine analysis. However, Olsen-extractable P was similar in magnitude to Q₁ (P-Olsen = 1.1 × Q₁ + 2.3, r² = .96), n and k₁ were related to P-Olsen/P-CaCl₂, while k₂ was related to P-oxalate/P-Olsen. Therefore, these extractions can be used to estimate the sizes and desorption rates of the different P pools, which could be important for assessments of plant availability and leaching.