Inorganic Phosphorus Fractionation of Highly Calcareous Soils of Iran

E. Adhami, M. Maftoun, Abdolmajid Ronaghi, N. Karimian, Jafar Yasrebi, M. T. Assad

Communications in Soil Science and Plant Analysis · 2006 · 61 citations · 18 references

Concepts

Abstract

Abstract Highly calcareous soils are abundant in Iran. The calcium carbonate equivalent (CCE) of these soils reach up to 650 g kg−1. Although phosphorus (P) fertilizer is being widely used in these soils, little information, if any, is available about P status in such soils. The objectives of this study were to 1) determine inorganic P forms in 18 surface soils of southern Iran, 2) study P readsorption during different stages of fractionation schemes, 3) assess the ability of NaOH to extract aluminum (Al)‐P, and 4) evaluate the relationships between P availability indices and inorganic P forms. Eighteen soil samples with a wide range of physicochemical properties were selected for this study. Inorganic P forms was determined by sequential extraction with NaHCO3, NH4OAc, NH4F, NaOH, citrate dithionite (CD), and H2SO4, which are referred to as Ca2‐P, Ca8‐P, Al‐P, Fe‐P, occluded P (O‐P), and Ca10‐P. Phosphorus readsorption in different stages was determined by 1 M MgCl2. Furthermore, a fractionation scheme without an NH4F step was used to evaluate the ability of NaOH to extract Al‐P. NaHCO3 (Olsen‐P) and MgCl2‐extractable P (Exch‐P) were regarded as P-availability indices. The abundance of different P forms was in the order Ca2‐P<Fe‐P<Al‐P<O‐P<Ca8‐P<Ca10‐P. Ca2‐P was highly correlated with Olsen‐P and Exch‐P. Ca2‐P, Olsen‐P, and Exch‐P showed a relationship with CCE, citrate–bicarbonate–dithionite extractable Fe (Fed), and Al (Ald). Phosphorus readsorption appeared to be important only in the Ca8‐P step, and the content of readsorbed P was related to Ca8‐P, CCE, and clay content of the soils. In the present study, Al‐P and Fe‐P accounted for 10 and 5% of the sum of the inorganic P fractions, respectively, and Fe‐P showed a strong relationship with Feo, whereas Al‐P showed a significant relationship with oxalate‐extractable Al (Alo) and Ald. It was found that one extraction with NaOH is not a good indicator for Fe‐ and Al‐P, and the ability of NaOH to extract Al‐P was reduced with increase in Al‐P content.

References

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