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This article in SSSAJ

  1. Vol. 71 No. 6, p. 1867-1877
     
    Received: Jan 2, 2007
    Published: Nov, 2007


    * Corresponding author(s): kimhj69@rda.go.kr
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doi:10.2136/sssaj2007.0002

Simultaneous Analysis of Soil Macronutrients Using Ion-Selective Electrodes

  1. Hak-Jin Kim *a,
  2. John W. Hummelb,
  3. Kenneth A. Sudduthb and
  4. Peter P. Motavallic
  1. a National Institute of Agricultural Engineering (NIAE), Suwon, South Korea 441-100
    b USDA-ARS Cropping Systems and Water Quality Research Unit, Columbia, MO 65211
    c Dep. of Soil Environmental and Atmospheric Sciences, Univ. of Missouri, Columbia, MO 65211

Abstract

Automated sensing of soil macronutrients would be useful in mapping soil nutrient variability for variable-rate nutrient management. Ion-selective electrodes (ISEs) are a promising approach because of their small size, rapid response, and ability to directly measure the analyte. This study reports on the laboratory evaluation of a sensor array including three different ISEs, based on TDDA–NPOE and valinomycin–DOS membranes, and Co rod, for the simultaneous determination of NO3–N, available K, and available P in soil extracts. Thirty-seven Illinois and Missouri soils were extracted using the Kelowna soil extractant (0.25 mol L−1 CH3COOH + 0.015 mol L−1 NH4F). The response of each electrode type in mixed solutions of NO3, K, and P ions was modeled based on the Nikolskii–Eisenman equation with all coefficients of determination (r 2) ≥0.95 (P < 0.001). In soil extracts, the NO3 ISEs provided concentrations similar to those obtained with standard laboratory methods (r 2 = 0.89, P < 0.001). Concentrations obtained with the K ISEs were about 50% lower than those obtained with standard methods due to lower K extraction by the Kelowna solution (r 2 = 0.85, P < 0.001). The P ISEs provided concentrations about 64% lower than those obtained with standard methods due to a combination of decreased P estimates in soil extracts and lower P extraction by the Kelowna solution; however, there was a strong linear relationship (r 2 = 0.81, P < 0.001). Although P and K concentrations were low in comparison to standard laboratory procedures, a calibration factor could address this issue. These results show that ISE technology can be implemented successfully for NO3–N, available K, and available P measurement with the Kelowna extractant.

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Copyright © 2007. Soil Science SocietySoil Science Society of America