Solubility and retention of phosphate in soils of the northwestern Canadian prairie

1991 ◽  
Vol 71 (4) ◽  
pp. 453-463 ◽  
Author(s):  
Y. K. Soon

Phosphate solubility and sorption characteristics of 39 agricultural soils in the northwestern Canadian Prairie were studied to gain insights into the retention of fertilizer P added to soil. The soils were mostly acidic with base saturation of 59–95%. The solubility of P as determined by the equilibrium P concentration and phosphoric acid potential was low and appeared to be controlled by sorption of phosphate by soil components. The mean equilibrium solution P concentration was 0.03 mg L−1. Phosphorus concentration in saturation extracts was about one order of magnitude higher, but would have included organic and colloidal P since P analysis in these extracts was done by ICP. Sorption capacity of P as determined by Langmuir isotherm was greater for the Dark Gray and Black soils and gleysols, i.e., soils with higher amounts of organic matter, than the Gray Luvisolic and Solodic soils by about 30%. Partial correlation showed that clay content, Al-organic matter complexes (AlOM) and amorphous iron oxide (FeOX) were significantly correlated with P sorption capacity. When both topsoils and subsoils were considered, clay content was the most important soil property influencing P sorption capacity, followed by AlOM and FeOX (standard partial regression coefficients, b′, of 0.47, 0.39 and 0.38, respectively). When only topsoils were considered, AlOM and FeOX became more important than clay content in influencing P sorption (b′ = 0.47, 0.47, and 0.33, respectively). Native P, estimated by oxalate and anion-resin extractions, was associated with the hydrous iron oxides only, although soil pH also affected the resin-extractable P fraction. Key words: P retention, solubility, Luvisols, solodic soils

Author(s):  
Berhanu Dinssa ◽  
Eyasu Elias

<span>One of the most soil fertility management problems for crop production on acidic soils of the Ethiopian highlands is phosphorus fixation. The research was executed to assess the P-sorption capacity and to determine the external P requirement of different acidic soils in the Southwestern highlands of Ethiopia. Phosphorus sorption capacity (Kf) and its relation with selected soil characteristics were assessed for some major agricultural soils in the Ethiopian highlands to answer the questions, ‘What are the amount of P-sorption capacity and external P requirement of Nitisols, Luvisols, Alisols, and Andosols in Ethiopia?’. Twelve surface soil samples (at depth of 0-30 cm) were gathered and the P-sorption capacity was estimated. Phosphorus-sorption data were obtained by equilibrating 1 g of the 12 soil samples with 25 ml of KH<sub>2</sub>PO<sub>4</sub> in 0.01 M CaCl2, having 0, 30, 60, 90, 120, 150, 180, 210, 240, 270, 300, and 330 mg P L<sup>-1</sup> for 24 hours. The data were adjusted to the Freundlich adsorption model and the relationship among P-sorption and soil characteristics was established by correlation analysis.  Clay content and exchangeable acidity, organic matter, Al<sub>2</sub>O<sub>3</sub>, and Fe<sub>2</sub>O<sub>3</sub> oxides have affected phosphorus-sorption at a significance level of (P &lt; 0.05).  Alisols had the highest Kf value (413 mg kg<sup>-1</sup>) but Nitisols had the lowest Kf (280 mg kg<sup>-1</sup>). The external phosphorus fertilizer requirement of the soils was in the order of 25, 30, 32, and 26 mg P kg<sup>-1</sup> for Nitisols, Luvisols, Alisols, and Andosols sequentially. The Kf varies among different soil types of the study area. The magnitude of the soil’s Kf was affected by the pH of the soil, soil OM content, and oxides of Fe and Al. Therefore, knowledge of the soils’ P retention capacity is highly crucial to determine the correct rate of P </span><span>fertilizer</span><span> for crop production.</span>


Soil Research ◽  
2005 ◽  
Vol 43 (6) ◽  
pp. 757 ◽  
Author(s):  
W. Wiriyakitnateekul ◽  
A. Suddhiprakarn ◽  
I. Kheuruenromne ◽  
R. J. Gilkes

The objective of this study was to determine if dithionite- and oxalate-extractable Fe and Al can be used to predict the P sorption capacity of Thai soils. Forty-five samples from diverse soil types were taken from surface and subsurface horizons of soils on sandstone, shale/limestone, granite, and basalt. The samples were analysed for P sorption, dithionite- and oxalate-extractable Fe and Al (Fed, Feo, Ald, Alo), specific surface area (SSA), and other soil properties. Generally P sorption data for these soils were slightly better fitted by the Langmuir equation than the Freundlich equation. The Langmuir P sorption maximum ranged from 35 to 1111 μg/g with a median value of 370 μg/g soil. Soils developed on basalt had higher values of P sorption maximum (xm) (range 400–1111 μg/g, median 597 μg/g) than soils on other parent materials. Fed concentrations in soils (4–74 g/kg) were much higher than Feo concentrations (0.2–13.8 g/kg) with values of Feo/Fed ranging from 0.01 to 0.28 (median 0.09), indicating that most of the free iron oxides were crystalline. Amounts of Ald and Alo were about equal with median values of 1.6 and 1.0 g/kg, respectively. About 80% of the samples had SSA values <40 m2/g. Both the P sorption maximum and Freundlich k were linearly related to SSA (R2 = 0.77, 0.74), Ald (R2 = 0.78, 0.79), Alo (R2 = 0.64, 0.74), Fed (R2 = 0.48, 0.41), Feo (R2 = 0.43, 0.72), and clay content (R2 = 0.48, 0.36). Stepwise regression indicated that 81% of the variability in P sorption by these soils could be explained by a combination of dithionite and oxalate Fe and Al, however, Ald alone is almost as effective in predicting the P sorption capacity of Thai soils.


1990 ◽  
Vol 62 (1) ◽  
pp. 9-15
Author(s):  
Raina Niskanen

The dependence of the indicator of phosphate sorption capacity on extractable Al and Fe and other soil properties was studied in a material consisting of 102 mineral soil samples. The sum of P adsorbed on soil during two days from a solution containing P 5 mmol/l and P extracted by 0.02 M EDTA (pH 5.3) as an estimate of the initial P content in the soil was used as the indicator of P sorption capacity. In clay and silt soils (n = 51), the Al and Fe extracted by 0.05 M oxalate (pH 2.9) together with the organic C content explained 85 %, the Al and Fe extracted by 0.05 M K4P2O7 (pH 10) together with the clay content 87 %, the Al and Fe extracted by 0.02 M EDTA (pH 5.3) 91 %, and the Al extracted by 1 M CH3COONH4 (pH 4.8) together with the organic C and clay contents 78 % of the variation of the indicator of phosphate sorption capacity. In coarse soils (n = 51), the variation of the indicator was explained well only by oxalate-extractable metals, which together with soil pH and clay content explained 80 % of the variation. Extractable Al was generally the most important explainer of variation. The results suggest that forms of extractable Al and Fe explaining the variation of the indicator of P sorption capacity in clay and silt soils are partially different from those in coarse soils.


2020 ◽  
Vol 20 (4) ◽  
pp. 1882-1890 ◽  
Author(s):  
Gilmar Luiz Mumbach ◽  
Luciano Colpo Gatiboni ◽  
Daniel João Dall’Orsoletta ◽  
Djalma Eugênio Schmitt ◽  
Patrícia Pretto Pessotto ◽  
...  

1997 ◽  
Vol 35 (5) ◽  
pp. 103-108 ◽  
Author(s):  
T. Zhu ◽  
P. D. Jenssen ◽  
T. Mæhlum ◽  
T. Krogstad

Five light-weight aggregates (LWAs), suitable for filter media in subsurface flow constructed wetlands, were tested for potential removal of phosphorus (P). P-sorption variation is dependent on the chemical characteristics of the LWA. All LWAs exhibited high pH and high total metal content; however, P-sorption capacity varied by two orders of magnitude. Of the LWAs' chemical characteristics (total metal content, cation exchange capacity, and oxalate soluble Fe and Al), total metal content has the closest relationship with the P-sorption capacity. Among the four major metal ions (Mg, Ca, Fe and Al), Ca has the strongest correlation with the P-sorption capacity.


Soil Research ◽  
2004 ◽  
Vol 42 (1) ◽  
pp. 89 ◽  
Author(s):  
L. L. Burkitt ◽  
C. J. P. Gourley ◽  
P. W. G. Sale

Five field sites established in the high rainfall zone of southern Victoria were used to examine the downwards vertical movement of phosphorus (P) fertiliser on soils which ranged in P sorption capacity. Fertiliser was applied either as a single application of 280 kg P/ha at the beginning of the experiment (April 1998), or as 35�kg�P/ha reapplied every 6 months (totalling 210 kg P/ha by the end of the third year). Soil cores were sampled in June 2001 to a depth of 40 cm, and soil at depths of 0–5, 5–10, 10–20, 20–30, and 30–40 cm was analysed for a range of soil properties and total P concentration.Total P concentration changed very little down the profile, indicating that there was minimal vertical movement of P fertiliser below the 10 cm layer of 5 pasture soils following the single application of 280 kg P/ha or 35 kg P/ha reapplied every 6 months. Soils with low to moderate surface P sorption capacity showed a trend for higher total P concentrations at depth. However, quantitative relationships between vertical P movement and soil properties at depth were poor. A P audit resulted in variable recovery of the applied P (45–128%) in the surface 40 cm at each of the 5 sites. Consistently low P recoveries were achieved at one site, where the surface soil had a high P sorption capacity. Some applied P may have bypassed the high P sorbing surface layers at this site through macropore flow and moved beyond the 40 cm sampling zone, or have been lost to surface runoff. These results question the usefulness of P audit or mass-balance methods for accounting for P movement in a pasture-based system, as spatial heterogeneity of soil properties, both horizontally and vertically, was high in the current study.


Soil Research ◽  
2012 ◽  
Vol 50 (1) ◽  
pp. 7 ◽  
Author(s):  
Thomas Keller ◽  
Anthony R. Dexter

The plastic limits (lower plastic limit, PL; and liquid limit, LL) are important soil properties that can yield information on soil mechanical behaviour. The objective of this paper is to study the plastic limits of agricultural soils as functions of soil texture and organic matter (OM) content. The plastic limits were highly related to the clay content. The LL was more strongly correlated with clay than was PL, but the reasons are unclear. Interestingly, PL was virtually unaffected by clay content for soils with clay contents below ~35%. The OM had a strong effect on the plastic limits. This effect was clearly demonstrated when analysing soils of similar texture with a range of OM. We present equations (pedotransfer functions) for estimation of PL, LL, and plasticity index (PI) from soil texture and OM. Finally, we predict that the clay content must be ≥10% for soils without OM to be plastic; however, soils with <10% clay can be plastic if OM is present. More research is needed to investigate OM effects on soil consistency.


2011 ◽  
Vol 57 (No. 7) ◽  
pp. 307-314 ◽  
Author(s):  
J. Matula

Phosphorus concentration in the soil solution of agricultural soils should be a consensus of the agronomic and environmental aspect. Data from literary sources are inconsistent if the method of soil solution extraction from the soil and the method of phosphorus detection are not indicated. In the present paper a simplified procedure of soil solution extraction is used that is derived from the need of water to attain saturated soil paste. Based on barley cultivation in a plant growth chamber on 72 different soils the relationship between P concentration in simulated soil solution and the response of test plant (spring barley) was evaluated. Three approaches were used to derive an adequate P concentration in soil solution. Based on the diagnostics of P content in barley the following adequate P concentrations in soil solution were derived: 0.23&ndash;0.86 ppm P for colorimetry and 0.9&ndash;1.75 ppm P for ICP-AES. Using the concept of the boundary line of yield the critical P concentration in soil solutions was 0.8 ppm P for colorimetry and 1.3 ppm P for ICP-AES. The concept of the boundary line of P efficiency index enabled to define P concentrations in soil solution that can be considered as the lower limits of suitability from the agronomic aspect:<br />0.15 ppm P in simulated soil solution for colorimetry and 0.7 ppm P for ICP-AES.


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