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Research Detail

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J.C. Joardar*
Soil, Water and Environment Discipline, Khulna University, Khulna-9208, Bangladesh

S. Sikder
Soil, Water and Environment Discipline, Khulna University, Khulna-9208, Bangladesh

S.B. Hasib
Soil, Water and Environment Discipline, Khulna University, Khulna-9208, Bangladesh

Low availability of phosphorus (P) due to P sorption onto soil is one of the major hindrances that greatly affect crop production. So, the understanding of P-soil interactions plays a vital role for increasing agronomic efficiency as well as proper P management. For optimal crop production, annual P application rates should be in equilibrium with the rate of P sorption by soil to ensure the presence of sufficient P in soil. So, it is important to identify the rate of P sorption with time. The focus of this study was to determine and compare the influence of solution P concentrations and equilibrium time on P sorption in calcareous and noncalcareous soils. In the experiment, 0, 2.5, 5, 10, 20 and 50 μg P ml-1 solutions were taken and the sorption rate was investigated at 6, 12, 24 and 48 hour time periods. The results indicate that the P retention onto soil significantly increased with increasing concentration of solution P. Equilibrium time also influenced P sorption. The maximum P sorption was found after 24 hours. After 48 hours, some desorption of fixed P was observed that reflects the reversibility of sorbed P with time. The higher P sorption was found in calcareous soil than in noncalcareous soil irrespective of equilibrium time and solution P concentration.

  Calcareous soil, Phosphorus, Sorption
  Agricultural field at Gutudia of Dumuria upazilla, Khulna
  
  
  Crop-Soil-Water Management
  Physico-Chemical

Considering proper understanding of P adsorption or retention in these soils, the present experiment aimed at evaluating the effects of solution P concentration and equilibrium time on P sorption in both calcareous and non-calcareous soils. 

The experiment was conducted in the laboratory of Soil, Water and Environment discipline, Khulna University, Bangladesh.

General information about soil sampling sites Soil samples were collected from the agricultural field at Gutudia of Dumuriaupazilla, Khulna. Calcareous soil belongs to Dumuria soil series and noncalcareous soil belongs to Barisal soil series. The land type is medium high land for both soils. The lands are mainly used for rice cultivation.

Collection and preparation of soil samples Both soils were collected at a depth of 0-15 cm on the basis of the composite sampling method. Field identification method was used to identify calcareous and non-calcareous soils. The emergence of effervescence or fizzing after placing few drops of dilute hydrochloric acid (10% HCl) indicated the presence of free CaCO3 in soil. After that, the collected soil samples were air-dried and the larger aggregates were broken gently by crushing with a wooden hammer and passed through a 0.5-mm sieve and the samples were preserved in plastic bags for experiment and analysis.

Soil analysis Particle size analysis of the soils was done by the combination of sieving and hydrometer method as described by Gee and Bauder (1986). Textural classes were determined by Marshall’s triangular coordinate system by the respective percentage of soil separates (Brady and Weil, 2002). Soil pH, EC and total P were determined by following the procedure (Huq and Alam, 2005). 

P sorption studies Equilibration procedure Both calcareous and non-calcareous soils were used for this experiment. Triplicate 1.0g soil sample was weighed into a series of 50-ml polyethylene centrifuge tubes. Twenty five (25) ml each of P solution, containing 0, 2.5, 5.0, 10.0, 20.0 and 50.0 μg P ml-1 , were added to the tubes. The pH of the soil suspensions was adjusted to 6.0 with 0.1M HCl or 0.1M NaOH. The amount of HCl or NaOH added for adjusting pH was taken into account in calculating the total volume of the equilibrating solution. The reason for choosing pH 6.0 in this experiment was that adsorption isotherms have been reported to be better defined at this pH than at other pH levels (Shuman, 1975). The tubes were shaken on a reciprocating shaker for two hours and were allowed to equilibrate at room temperature for 6, 12, 24 and 48 hours. Immediately following the equilibration period, the suspensions were centrifuged and filtered. The filtrates were analyzed for P by spectrophotometry. 

Statistical analysis The results were expressed as the average of four replications. The data was subjected to ANOVA using computer built-in statistical software program Minitab– 16. Differences between means were statistically analyzed using the Fisher method (p=0.05). Graphs were prepared by using a computer built-in Microsoft Excel–2010 program.

  SAARC J. Agric., 17(2): 117-126 (2019)
  DOI: https://doi.org/10.3329/sja.v17i2.45299
Funding Source:
1.   Budget:  
  

The study was done to compare the P sorption in two representative soils (calcareous and non-calcareous) with equilibrium time and solution P concentration. Results revealed that the P sorption was greatly affected by both the solution P concentration and equilibrium time. Phosphorus sorption was significantly increased with increasing solution P concentration in both calcareous and non-calcareous soils. Maximum sorption was found for the concentration of 50 µg P ml-1 in solution. Equilibrium time had also a significant effect on P sorption in both soils. Sorption of P was increased with equilibrium time up to 24 hours then it was decreased after 48 hours. The decreased P after 48 hours indicated that the P was adsorbed to its maximum level within 24 hours and it might be desorbed from the adsorption sites. Between calcareous and non-calcareous soils, the maximum sorption was found for calcareous soil irrespective to solution P concentration and equilibrium time.

  Journal
  


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