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Application of Ion-Selective Electrodes for Simultaneous Analysis of Soil Macronutrients

机译:离子选择性电极在土壤常规营养素同时分析中的应用

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Automated sensing of soil macronutrients would be useful in mapping soil nutrient variability for variable-rate nutrient management. This study reports on the evaluation of a sensor array composed of three different ion selective electrodes (ISEs), inconjunction with the Kelowna soil extractant, for the simultaneous determination of soil N, P, and K. Data were obtained for two sets of soils - single samples from 37 fields across Illinois and Missouri (MOIL) and 36 samples from a single Illinois research field (NIARC). The response of each ISE type in mixed solutions of N, P, and K ions was modeled based on the transformed Nikolskii-Eisenman equation with all coefficients of determination (r~2) >= 0.95. The nitrate ISEs provided concentrations similar to those obtained with standard methods (r~2 = 0.89). The soil ISE-K concentrations were about 47% lower than those by standard methods due to lower K extraction efficiencies by Kelowna solution. The combination of lower P estimates in soil extracts and reduced P extraction efficiencies by Kelowna provided 63% lower ISE values as compared to standard methods. However, there were strong relationships between ISE and standard methods for K and P concentrations (r~2 >= 0.80). The applicability of modelsbased on the MO-IL dataset to new ion-selective membranes in the NIARC test was limited by high bias errors, perhaps due to the use of a 2-point normalization method that could not effectively compensate for sensitivity differences between membranes. Additional research will be required to develop calibration methods that can provide more accurate results across different membranes.
机译:土壤Macronrients的自动化感应对于绘制土壤养分可变性,可用于可变速率管理。该研究报告了由三种不同离子选择性电极(ISE)组成的传感器阵列的评估,用于同时测定土壤N,P和K的同时测定两组土壤 - 来自伊利诺伊州境外37个字段的单一样本和来自单一伊利诺伊州研究领域的36个样品(核心核苷类)。基于具有所有测定系数(R〜2)> = 0.95的变化的Nikolskii-eisenman方程,对每个ISE类型的N,P和K离子进行混合溶液的响应。硝酸酯是与用标准方法获得的浓度相似(R〜2 = 0.89)。由于Kelowna溶液较低的k萃取效率,土壤ISE-K浓度比标准方法低约47%。与标准方法相比,土壤提取物中较低的P估计和kelowna的降低的P提取效率的组合提供了63%的ISE值。然而,k和P浓度的ISE和标准方法之间存在强烈的关系(R〜2> = 0.80)。模型在Mo-IL数据上的适用性在Niarc测试中的新离子选择性膜上受到高偏差误差的限制,可能是由于使用2点归一化方法,不能有效地弥补膜之间的敏感性差异。需要额外的研究来开发可以在不同膜上提供更准确的结果的校准方法。

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