TDR estimation of the resident concentration of electrolyte in the soil solution
I. Vogeler, B. E. Clothier and S. R. Green
Australian Journal of Soil Research
35(3) 515 - 526
Published: 1997
Abstract
In order to examine whether the electrolyte concentration in the soil solution can be estimated by time domain reflectometry (TDR) measured bulk soil electrical conductivity, column leaching experiments were performed using undisturbed soil columns during unsaturated steady-state water flow. The leaching experiments were carried out on 2 soils with contrasting pedological structure. One was the strongly structured Ramiha silt loam, and the other the weakly structured Manawatu fine sandy loam. Transport parameters obtained from the effluent data were used to predict the transient pattern in the resident electrolyte concentration measured by TDR. The electrolyte concentration was inferred from the TDR-measured bulk soil electrical conductivity using 2 different calibration approaches: one resulting from continuous solute application, and the other by direct calibration. Prior to these, calibration on repacked soil columns related TDR measurements to both the volumetric water content and the electrolyte concentration that is resident in the soil solution. The former calibration technique could be used successfully to describe solute transport in both soils, but without predicting the absolute levels of solute. The direct calibration method only provided good estimates of the resident concentration, or electrolyte concentration, in the strongly structured top layer of the Ramiha soil. This soil possessed no immobile water. For the less-structured layer of the Ramiha, and the weakly structured Manawatu soil, only crude approximations of the solute concentration in the soil were found, with measurement errors of up to 50%. The small-scale pattern of electrolyte movement of these weakly structured soils appears to be quite complex.Keywords: TDR calibration, solute transport, soil water content, soil structure.
https://doi.org/10.1071/S96089
© CSIRO 1997