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a Inst. of Soil Sci. and Forest Nutr., Univ. of Göttingen, Büsgenweg 2, 37077 Göttingen, Germany
b Dep. of Biol. Sci., Florida International Univ., Miami, FL 33199 USA
eveldka{at}gwdg.de
| ABSTRACT |
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) range of 0.45 to 0.70 m3 m-3. Separate values of the geometry parameter (
) and of the specific output period for soil matrix (Pers) were established both for the topsoil (00.5 m depth) and for the subsoil (>0.5 m depth). The manufacturer's calibration function underestimated the soil water content by up to 0.15 m3 m-3. The three-phase mixing model uses a physical basis for the derivation of the calibration function in that the soil porosity is used for volumetric partitioning among soil components. This physical basis renders the calibration function widely adaptable.
Abbreviations: FDR, frequency domain reflectometry Pera, specific output period for air Pers, specific output period for soil matrix Perw, specific output period for water TDR, time domain reflectometry
| INTRODUCTION |
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For TDR, various calibration functions relating Ka to the volumetric soil water content have been published. Although an empirically derived calibration function is the most widely used (Topp et al., 1980), empirical relations are valid only in the range of soil characteristics covered in the calibration. Special TDR calibration functions derived for high clay content soils (Dasberg and Hopmans 1992; Bridge et al., 1996; and Weitz et al., 1997), resulted in apparent dielectric constant values lower than those obtained and reported by Topp et al. (1980). A promising approach is the use of mixing models, which take soil physical properties into account in the calibration. In mixing models it is assumed that the soil is a mixture of randomly distributed components, each having specific dielectric properties. The measured Ka is assumed to be the result of a volumetric mixing of the different components. A three-phase mixing model developed by Roth et al. (1990) has been successfully applied to calibrating TDR in soils in our study area (Weitz et al., 1997), even though these soils' physical properties were quite different from the soils used in Roth et al.'s (1990) calibration. Our goal was to make a calibration for the FDR sensor, with the following criteria: (i) it should be applicable to soils with high clay and organic matter contents and with bulk densities between 0.7 and 1.1 g cm-3, and (ii) the calibration function should be widely adaptable by having a physical basis rather than merely an empirically derived function.
| Materials and methods |
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1.1 g cm-3 below 2 m depth) and high organic C content (4%6% in the topsoil decreasing to
0.5% below 2 m depth). The main clay mineral in the topsoil is kaolinite, while gibbsite is dominating in the subsoil (M. Kleber, personal communication, 2000). The frequent and abundant rainfall combined with the high organic matter and clay content means that the volumetric water content only very rarely reaches values <0.45. On the other hand, even during rain storms, the volumetric soil water content never reaches values >0.70 m3 m-3, which is attributable by the high soil porosity.
Frequency Domain Reflectometry Sensor
We used a commercially available FDR sensor (Model CS615, Campbell Scientific, Logan, UT). This sensor is based on simple transmission line oscillators, which were developed and tested by Campbell and Anderson (1998). The FDR sensor consists of two stainless steel rods (0.3 m long, 0.0032 m in diam., 0.032-m spacing) that are connected to a printed circuit board and are protected by an epoxy block. On the circuit board high speed electronic components are configured as a bistable multivibrator. The output of the multivibrator is connected to the probe rods, which act as wave guides. When the multivibrator switches states, the transition travels the length of the rods and is reflected by the rod ends. The travel time to the end of the rods and back is dependent on the dielectric constant of the material surrounding the rods. The reflected wave is detected by a threshold circuit and, in turn, triggers the multivibrator into the alternate state. This sequence repeats as long as the sensor is enabled. A scaling circuit adapts the multivibrator frequency to a value compatible with a data acquisition device, such as a datalogger or a multimeter. The sensor output is a square wave with a frequency that varies with water content and has an approximate range of 700 to 1500 Hz (Bilskie, 1997; Campbell Scientific, 1998).
The propagation of electromagnetic waves is not only affected by soil water content but also by electrical conductivity, temperature, and clay content. If electrical conductivity is >1 dSm-1, the slope of the sensor output (ms) against volumetric water content decreases. This response of the sensor is well behaved up to
5 dSm-1 and can be compensated for. High clay content has a similar effect on the calibration, but the magnitude is dependent on the clay type. The temperature dependence of the FDR sensor varies with water content (Campbell Scientific, 1998) and can be easily corrected for.
Calibration Procedure
For the calibration procedure we largely followed that described by Weitz et al. (1997) with a few simplifications. We prepared undisturbed soil samples of 0.305 by 0.17 by 0.08 m using plastic boxes as molds. Soil samples at 0.05-, 0.20-, 0.75- and 2.5-m depths were taken horizontally in the soil pits, while soil samples at the surface (00.3 m depth) were taken vertically. The soil samples remained in the plastic boxes and were transported to the laboratory. Two small holes were drilled in one of the short sides of the boxes to facilitate insertion of the FDR sensors. The sensors were inserted horizontally in the center of each block, leaving
0.04 m between the rods and the top and bottom of the soil block. As the sensitive region extending radially from the rods is approximately 0.02 m (Bilskie, 1997), the size of our soil blocks was more than sufficient to ensure that measurements were limited to the soil sample. Small holes were drilled in the bottom of each box and the samples were saturated with water from the bottom up in a basin with
0.01-m water level. The basin had to be refilled several times by hand.
During the saturation period of
48 h the samples were loosely covered with lids to reduce evaporation. Excess water was drained following saturation and the lid was removed to allow evaporation. Average temperature in the laboratory was 24°C, which is close to the average temperature measured in the field. We took daily measurements of the frequency output of the sensor (Hz) using a multimeter and converted these to output period (ms) by calculating the reciprocal. We also weighed the soil samples including the box and sensor for gravimetric measurement of the soil water content. After 1 to 2 wk, as the soil samples became dry, the multimeter readings were out of the range measured in the field. The soil samples were then dried for 48 h at 105°C and weighed. The gravimetric water content was converted to volumetric water content (
) using dry bulk density values that were measured from the same soil pits. Porosity was calculated assuming a density of mineral particles of 2.65 g m-3. Bulk density was measured at each soil depth on six undisturbed soil samples, using sample rings with volume of 300 cm3. Bulk density rings were carefully inserted by hand without a hammer in order to prevent compaction during sampling. We did not use the bulk density of the soil samples used for calibration because the plastic mold was easily deformed and had no fixed volume.
Theory and Calculations
The standard empirical calibration function for the FDR established by the manufacturer for soils with an electrical conductivity
1.0 dS m-1 is
![]() | (1) |
is the volumetric water content in m3 m-3 (Campbell Scientific, 1998). This function does not contain any soil physical information and according to Campbell Scientific (1998) is not suitable for soil with a high clay and organic matter content. As mixing models have been successfully used for TDR calibrations in a wide range of soils, we decided to develop a mixing model for the tested sensor. Following the approach used for three-phase mixing models in TDR calibrations (Roth et al., 1990; Dasberg and Hopmans, 1992; Weitz et al., 1997), we assume that the FDR probe output is the result of a mixing of the independent components in the soil: soil matrix, air, and water. We use soil porosity to partition between the soil matrix and the soil pores that are filled with air and/or water. A geometry parameter (
) is used to define the shape of the calibration function between very low and very high output periods.
is supposed to be a soil specific geometry parameter that accounts for the soil structure. The resulting three-phase mixing model reads
![]() | (2) |
is volumetric water content
is geometry parameter
is soil porosity
The frequency or period of the multivibrator is related to the dielectric constant of the medium in which the sensor is placed. However, the output period of the FDR sensor is not equal to the period of the multivibrator but has been scaled by digital circuitry to an appropriate frequency for measurements with a datalogger (Campbell Scientific, 1998). Therefore, the output period of the sensor as such does not have a soil physical meaning, and in contrast to TDR mixing models we cannot derive a theoretical value for the three different phases: water, air, and soil matrix. Nevertheless, this problem can be solved by measurement of the sensor output in air and in water, which gives the specific output period for air (Pera) and water (Perw). Pera and Perw were measured by taking the mean of five 1-min averages of 12 measurements both in air and in water. The water temperature was 24°C and the electrical conductivity was <1.0 dS m-1. Pers and
can be derived empirically from the best fit of the three-phase model to the observations. It should be kept in mind that Pers and
vary spatially within a soil as the soil density and structure vary spatially. We used the least square method to fit the model to the observations. Root mean square error (RMSE) was calculated to evaluate the performance of the calibration models.
| Results and discussion |
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in such a way that the sum of squares of the differences between the measured and calculated soil moisture content from the three-phase mixing model was minimized. Best results were obtained when we made a separate calibration for samples of the topsoil and subsoil. The best fit was found for
= 0.5 and Pers = 0.918 for the topsoil (00.5 m), and
= -2.2 and Pers = 1.307 for the subsoil (>0.5 m depth). The negative value of
in the subsoil is different from values found in mixing models for TDR application. We explain this by pointing out the different shape of the FDR probe response compared that of the TDR. Values of Pers were different between topsoil and subsoil, which we explain via the relatively large difference in soil organic C content (Table 2)
. As porosity is already included in the calibration through the partition between soil matrix and the soil pores, this is probably not the cause of the different values of Pers. The RMSE of our three-phase mixing model for FDR calibration (Table 2) were lower than the RMSE of the TDR calibration (between 0.044 and 0.045) in similar soils (Weitz et al., 1997). A comparison of measured volumetric water contents of the soils with those calculated from the three-phase mixing model showed that the values are scattered around the 1:1 line with an r2 of 0.99 for the topsoil and an r2 of 0.95 for the subsoil (Fig. 1). Mixing models have an inherent advantage compared to empirical calibration functions in that the former include soil porosity for volumetric partitioning among soil components. This physical basis of mixing models allows its calibration function to be more widely adaptable. This is demonstrated by the RMSE, which is small for soils with high and low bulk densities (Table 2). We encourage anybody who uses FDR or similar sensors for measuring soil water content to calibrate it using a three-phase mixing model instead of relying solely on the manufacturer's empirical calibration function. The importance of a good calibration is illustrated by a comparison of the volumetric water contents calculated from the manufacturer's calibration function and the three-phase mixing model calibration on field-measured FDR output (Fig. 2)
. This figure shows hourly rain and soil moisture data in the topsoil during December 1997. The results with the three-phase mixing model are consistently higher than the standard calibration.
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| Conclusions |
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| ACKNOWLEDGMENTS |
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Received for publication May 28, 1999.
| REFERENCES |
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