|
|
||||||||
a USDA-ARS, Soil and Water Management Research Unit, St. Paul, MN 55108
b Dep. of Agronomy, Iowa State Univ., Ames, IA 50011
c Inst. of Geographic Sciences and Natural Resources Research, Chinese Academy of Sciences, Beijing, China 100101
* Corresponding author (ochsner{at}umn.edu).
Journal paper of the Iowa Agriculture and Home Economics Exp. Stn., Ames, IA, Project No. 3287. Supported by the Soybean Research and Development Council, the Agronomy Dep. Endowment Funds, the Hatch Act, and the State of Iowa.
1 Mention of products and suppliers is for the convenience of the reader and implies no endorsement on the part of the authors or the USDA-ARS. ![]()
Received 14 March 2003.
| ABSTRACT |
|---|
|
|
|---|
). However, few published data are available regarding the performance of the DPHP technique under field conditions. The objective of this study is to evaluate the effectiveness of the DPHP technique for measuring
under field conditions. We used 24 DPHP sensors to monitor
in a soybean [Glycine max (L.) Merr.] field during the 2001 and 2002 growing seasons. The DPHP sensors demonstrated durability in field conditions and clear sensitivity to temporal and spatial variations of
at the scale of measurement. The mean
measured by the DPHP sensors (
DPHP) was on average 0.040 m3 m-3 larger than the mean
measured by soil sampling (
SS). The response of the DPHP sensors was linear. Regressions of
DPHP vs.
SS yielded r2 values of 0.949 and 0.843 at depths of 7.5 and 37.5 cm. The DPHP technique showed good resolution with RMSE values for the regression of 0.009 and 0.011 m3 m-3 at the two measurement depths. The slopes of the regressions were 0.75 rather than 1.0. Errors in
SS are a likely cause of this low slope. We shifted all the
values for each sensor up or down by a constant value to make the first
measurement from each sensor equal
determined from soil sampling near that sensor at the time of installation. This simple matching point procedure improved the accuracy of the DPHP technique, resulting in a -0.024 m3 m-3 average difference between
DPHP and
SS. Also, the matching point procedure markedly reduced the variability between sensors, reducing the average SD from 0.063 to 0.026 m3 m-3. This procedure requires no additional soil sampling and is recommended for field applications of the DPHP technique.
Abbreviations:
, volumetric water content
DPHP, mean soil volumetric water content measured by the dual-probe heat-pulse technique
SS, mean soil volumetric water content measured by soil sampling AWG, American Wire Gauge C, soil volumetric heat capacity DPHP, dual-probe heat-pulse
| INTRODUCTION |
|---|
|
|
|---|
in the vadose zone are often needed by researchers who study components of the terrestrial hydrologic cycle or who study the many biological, physical, and chemical processes that are influenced by
. Measurements of
are also often utilized by irrigation managers in agriculture and horticulture. A number of useful direct and indirect techniques for measuring
are available, each having characteristic strengths and weaknesses (Topp and Ferré, 2002). This study focuses on the DPHP technique, an indirect technique that enables automated, nondestructive measurements of
on a small volume of soil. The DPHP technique for measuring
was first suggested by Campbell et al. (1991), and has since been utilized by several researchers (Tarara and Ham, 1997; Ren et al., 1999; Song et al., 1999; Campbell et al., 2002). These studies have shown that the DPHP technique can provide accurate measurements of
and change in
(
) in laboratory and greenhouse settings.
However, evaluations of the effectiveness of the DPHP technique in the field have been limited. In one field study, Tarara and Ham (1997) compared
measurements from three DPHP sensors with
measurements made with a
attenuation meter and found that the two methods agreed to within 0.05 m3 m-3. In another field study, Campbell et al. (2002) compared
measurements from 10 DPHP sensors in a peat bog with
measurements from four water content reflectometer sensors (CS615, Campbell Scientific Inc., Logan, UT).1 They reported similar temporal patterns of
but different mean values between the two types of sensors at the 5-cm depth. At the 30-cm depth, they reported similar mean values of
but different temporal patterns of
between the two types of sensors. In total, we can find only two figures in two papers comparing DPHP
measurements with independent
measurements in the field. More extensive field comparisons between the DPHP technique and other accepted techniques for measuring
are needed to clearly define the effectiveness of the DPHP technique under field conditions. The objective of this study is to evaluate the effectiveness of the DPHP technique for measuring
under field conditions.
| THEORY |
|---|
|
|
|---|
. A brief heat pulse emitted from the heating needle of the DPHP sensor is transferred through the soil, resulting in a small temperature increase (
T) approximately 6 mm away at the sensing needle of the sensor. The maximum value of this temperature increase (
Tm) is inversely related to C (Campbell et al., 1991):
![]() | [1] |
by
![]() | [2] |
w is the density of water (kg m-3), cw is the specific heat of water (J kg-1 K-1),
b is the soil bulk density (kg m-3), and cs is the specific heat of the soil solids (J kg-1 K-1) (Campbell et al., 1991). Note that soil solids include both mineral and organic matter. Substituting Eq. [1] into Eq. [2] and rearranging gives the theoretical equation for determining
by use of the DPHP technique (Bristow et al., 1993):
![]() | [3] |
Equation [3] is based on the assumptions that the heat transfer around and through the DPHP sensor is the same as the heat transfer around an infinite line source in a homogeneous medium, that the finite duration heat pulse approximates an instantaneous heat pulse, that the heat transfer is only by conduction, that no contact resistance exists between the sensor and the soil, and that
w, cw, and cs are independent of
and temperature. Furthermore, in applying Eq. [3], we normally assume that all the variables other than q,
Tm, and
are constant throughout the measurement period.
| MATERIALS AND METHODS |
|---|
|
|
|---|
m-1, Nichrome 80 Alloy, Pelican Wire Co. Naples, FL) four times through the entire length of the tubing so that the resulting heater had a resistance of approximately 820
m-1. The total resistance of the completed heaters was about 33
. The temperature sensing needle was constructed by inserting a 36 American Wire Gauge (AWG) copper-constantan thermocouple junction (Type T, Omega Engineering, Stamford, CT) in the second tube. The interiors of the heating and temperature sensing needles were then filled with high thermal conductivity epoxy (Omegabond 101, Omega Engineering, Stamford, CT), and the heater and thermocouple wire were connected to 8.5-m-long 22-AWG stranded conductors (Pelican Wire Co., Naples, FL). The lead wires for the heating needle were copper, and the lead wires for the sensing needle were copper and constantan. The heating and temperature-sensing needles were inserted into predrilled holes in a small PVC block so that the needles were parallel and separated by about 6 mm. The needles protruded 27 mm from the PVC block, the thermocouple junction was in the center of the protruding portion of the sensing needle, and the wiring junctions between the needles and the leads were inside the hollow center of the PVC block. The cavity in the block was then filled with high thermal conductivity epoxy (RBC-4300 and A-121 epoxy hardener, RBC Industries, Warwick, RI) so that the finished sensors were waterproof and electrically insulated. Finally, the sensor leads were threaded through heavy-duty woven nylon sleeves (Protec NHS-071, Tompkins Industries Inc., Olathe, KS) to protect the leads from damage in the field.
Measurement System
The measurement system for the 24 DPHP sensors consisted of a datalogger (21x, Campbell Scientific), two multiplexers (AM416, Campbell Scientific), a reference thermistor (Model 107, Campbell Scientific), a pair of 0.27-
resistors wired in parallel (Philips ECG, Greenville, TN), a 5-V direct current relay capable of handling up to 2 A (R40-11D2-5, NTE Electronics Inc., Bloomfield, NJ), and a deep-cycle 12-V battery. The heater leads were connected to one multiplexer, and the thermocouple leads were connected to the second multiplexer. The thermocouple multiplexer was sealed in a well-insulated protective box with the reference thermistor mounted on the center bridge of the multiplexer. The heater multiplexer and the datalogger were each sealed in separate protective boxes. The datalogger switched the multiplexer channels at the appropriate times and activated the relay to switch current to the heaters. The current to the heaters flowed through the two 0.27
resistors wired in parallel, and the data-logger measured the voltage drop (
V) across the resistors. The relationship between
V and the heating power, q, is
![]() | [4] |
), Rh is the resistance per unit length of the heating element (
m-1), and t0 is the duration of the applied heat pulse (s). The sensors were heated for 8 s. The current through each heater was approximately 0.33 A, resulting in q
700 J m-1. The temperature of each sensor was measured before heating and one time per second for 80 s after the initiation of heating.
Calibration
The needle spacing, r, for each DPHP sensor was determined by recording measurements of q and
Tm with the sensor immersed in water stabilized with agar (6 g L-1) to prevent convection. Eq. [1] was then rearranged to solve for r with C =
wcw = 997.5 kg m-3 x 4180.4 J kg-1 K-1 = 4.170 x 106 J m-3 K-1 (data for water at 23°C; Weast, 1978). We assumed that the agar did not significantly alter the heat capacity of the water. Campbell et al. (1991) calibrated DPHP sensors in water stabilized with agar at 2 g L-1, but we found that at that concentration r was not stable when the heating power was varied. At 2 g L-1 agar, r decreased as
Tm increased, while r was independent of
Tm at 6 g L-1 agar (Fig. 1). These data suggest that the heat pulse induced some convection in water stabilized with agar at 2 g L-1. The mean value of r for the sensors was 5.98 mm with a SD between sensors of 0.19 mm. The calibration for each sensor was repeatable with an average coefficient of variation of 1.1% across 24 replications.
|
In 2001, the soybean was planted on 18 May, and the 24 DPHP sensors were installed on 27 July. The sensors were installed at two locations in each plot. At each location, sensors were installed at depths of 7.5, 22.5, and 37.5 cm below the soil surface. In 2002, the soybean was planted on 24 May, and 24 DPHP sensors were installed on 27 June. The sensors were installed at three locations in each plot. At each location, sensors were installed at depths of 7.5 and 37.5 cm below the soil surface. In 2002, one additional DPHP sensor was sealed into a water-tight 250-mL Nalgene (Rochester, NY) bottle filled with quartz sand (Unimin silica sand, Target Products Ltd., Burnaby, British Columbia). This sensor was used to verify the stability of the results from the measurement system and was placed aboveground under a protective cover along with the datalogger and multiplexer enclosures.
Every 6 h, measurements were performed on all the DPHP sensors, and the date, time, initial temperature, voltage drop across the resistors,
Tm, and the time between the initiation of the heat pulse and the occurrence of
Tm were recorded. The data were postprocessed to calculate q and
. The average of the
values measured by all the DPHP sensors at each depth will from here on be referred to as
DPHP.
Soil Sampling
In 2002, we collected soil samples from the field on eight different occasions for determining
by oven drying. The soil sampling procedure was designed to determine the average
at 7.5 and 37.5 cm for comparison with
DPHP. Soil spatial variability and the destructive nature of soil sampling preclude a meaningful comparison of the water content determined by an individual sensor with that determined by repeated soil sampling. At each sampling, one soil sample was taken near each DPHP sensor, thus 12 samples were taken at the 7.5-cm depth and 12 at the 37.5-cm depth. The first set of soil samples was obtained by hand during sensor installation. The final set of soil samples was taken by hand during sensor extraction. The other sets of soil samples were collected with a 30-cm-long soil sampler with a 1.9-cm i.d. (JMC Sampler, Clements Associates Inc., Newton, IA). With the soil sampler we obtained samples from the opposite side of the soybean row at the same depth as the sensor. The total distance from the sample location to the sensor was <1 m. The 7.5-cm sample was obtained by vertically inserting the sampler 15 cm into the soil and saving the 6.5- to 8.5-cm layer from the resulting soil core. The 37.5-cm sample was obtained by reinserting the sampler into the hole made by removing the first sample and saving the 36.5- to 38.5-cm layer from the resulting soil core. The total volume of each soil sample then was about 5.7 cm3. The sampling volume of a DPHP sensor can be approximated as follows: A cylinder with a diameter equal to the distance between the sensor needles, r, and a length equal to that of the sensor needles would enclose a volume of 0.79 cm3. This volume is an approximate lower limit on the sampling volume of the sensor. Theoretically, the radial distance from the heater at which the maximum temperature increase is 1% of
Tm is 2.37r or 1.4 cm (Campbell et al., 1991). A cylinder with a radius of 1.4 cm and a length equal to that of the sensor needles would enclose a volume of 17 cm3. This volume is an approximate upper limit on the sampling volume of the sensor. Therefore, the sensors probably sample a volume of soil between 0.79 and 17 cm3. The 5.7-cm3 volume of the soil samples falls within this range. The similarity of number, spatial distribution, and volume of samples is important for making an accurate comparison between the two techniques. The gravimetric water content of the soil samples was determined by weighing, drying for 24-h at 105°C, and weighing again. Bulk density was determined from separate soil samples taken at the site of each DPHP sensor during sensor extraction on 4 September. The average
b values for the 7.5- and 37.5-cm depths in 2002 are shown in Table 1. The average
determined from the 12 soil samples at each depth will from here on be referred to as
SS. Soil samples taken during the course of the study were used to determine selected physical properties of the soil in the laboratory. Particle size analysis was performed with the hydrometer method. Organic matter content was determined by dry combustion. And, cs was measured by a differential scanning calorimeter (Seiko DSC220C, Perkin-Elmer Analytical Instruments, Shelton, CT). The results listed in Table 1 are the means of two replications of the particle size and organic matter measurements and three replications of the cs measurements.
|
| RESULTS AND DISCUSSION |
|---|
|
|
|---|
DPHP and the daily rainfall totals for the period of measurement in both years are shown in Fig. 2. The data in Fig. 2 qualitatively demonstrate the sensitivity and reliability of the DPHP technique under field conditions. During the periods of measurement, the DPHP technique captured distinct temporal variations in water content. The
DPHP data show sharp increases in response to rainfall events and smooth, gradual decreases between rainfall events. The DPHP technique also captured distinct variations in water content with depth in both years. For example, the small rainfall events that occurred between 25 and 27 July 2002 resulted in a 0.05 m3 m-3 increase in
DPHP at the 7.5-cm depth but no increase in
DPHP at the 37.5-cm depth. The DPHP results in both years also reveal the general tendency for the 37.5-cm depth to be drier than the 7.5-cm depth. In the context of this study, the ability of the DPHP technique to capture temporal and spatial variations in soil water dynamics makes it a promising technique for studying infiltration, crop water use, and evapotranspiration. The data in Fig. 2 also indicate that a DPHP system can function reliably for months at a time in a field environment with minimal intervention. The measurement system was deployed for a total of 123 d during 2001 and 2002, and all of the sensors were still functioning properly at the end of the study. During the study, only two losses of data occurred. The first loss of data occurred for 12 d (27 Aug.7 Sept. 2001) and stemmed from a faulty splice in the reference thermistor cable. The second loss of data occurred for 5 d (22 Aug.26 Aug. 2002) and resulted from animals causing the external battery to be disconnected from the datalogger. Visits to the site were sporadic, and maintenance was limited to downloading data and changing the external battery when it became depleted (once per season in this case).
|
under outdoor ambient conditions. The ambient temperature of the sand ranged from 10 to 40°C during the measurement period. The practical value of installing a reference sensor is that it can help identify any gradual drift or sudden changes in the performance of the measurement system.
Comparison of
DPHP and
SS
From here on we will focus our analysis on the results from 2002, because that is the year in which we collected extensive soil samples. Figure 3 shows the time series of
DPHP and
SS for 2002. Four
DPHP measurements per day are plotted in Fig. 3, with each measurement being the average value from 12 sensors at the same depth. Figure 3 illustrates the value of automated measurements of
for describing soil water dynamics. Notice that soil samples were collected on 6 and 13 August and that the resulting
SS values show a small increase in water content during that period. In contrast, the relatively continuous
DPHP data for the same period show that the period between 6 and 13 August included a distinct dry-down followed by a clear rewetting. Figure 3 also demonstrates that the DPHP technique performs with a reasonable level of accuracy under field conditions. At the 7.5-cm depth,
DPHP was on average 0.025 m3 m-3 larger than
SS. At the 37.5-cm depth,
DPHP was on average 0.054 m3 m-3 larger than
SS. The reason for the greater difference between
DPHP and
SS at 37.5 cm than at 7.5 cm is unclear. The maximum absolute difference between
DPHP and
SS was 0.047 m3 m-3 at the 7.5-cm depth and 0.077 m3 m-3 at the 37.5-cm depth. At both depths, the maximum absolute difference occurred at the time of sensor installation.
|
DPHP and
SS. At the 7.5-cm depth, linear regression of
DPHP vs.
SS yields a coefficient of determination (r2) of 0.949 and a root mean square error (RMSE) of 0.00907 m3 m-3 (Table 2). At the 37.5-cm depth, linear regression of
DPHP vs.
SS yields a slightly lower r2 of 0.834 and a slightly higher RMSE of 0.0110 m3 m-3. The small RMSE values highlight the good precision achievable with the DPHP technique in the field. These r2 and RMSE values indicate how well mean water content could be estimated with 12 DPHP sensors. They do not represent the accuracy or precision of a single DPHP sensor. At both depths the slope of the regression line is about 0.75 and the intercept is about 0.1 (Table 2). In a laboratory evaluation of the DPHP technique, Basinger et al. (2003) reported slopes ranging from 0.86 to 0.94 and intercepts ranging from 0.03 to 0.07. For the present study, the slope is lower and the intercept is higher than those reported by Basinger et al. (2003). However, both the present study and the results of Basinger et al. (2003) suggest that the DPHP technique overestimates
and underestimates 
.
|
|
SS and the SD of water content determined by the sensors; that is, the variability between DPHP sensors did not depend on soil water content. The variability shown in Fig. 4 must be attributed both to actual spatial variability of
in the root zone of a growing soybean crop and to measurement errors.
Consideration of Error Sources
To understand why the slope of the linear regression of
DPHP vs.
SS is lower-than-expected, we must consider at least three potential error sources: the
SS measurements may have contained errors, the measurements of q and
Tm may have contained errors, and the assumptions behind the DPHP technique may have been violated. Errors in the
SS measurements are the primary potential contributor to the lower-than-expected slope. The first set of soil samples taken during sensor installation and the last set of soil samples taken during sensor extraction may have been subject to evaporation, and the resulting
SS may have been too small. The processes of sensor installation and sensor extraction each took approximately 8 hr, during which time the soil samples were kept in moisture cans in a shaded area. Given the length of time between sampling and weighing, some potential for evaporation did exist. As noted above, the maximum absolute difference between
DPHP and
SS occurred at sensor installation, and the second largest absolute difference occurred at sensor extraction. Furthermore, the set of soil samples taken on 13 August may have been biased toward overestimating the true water content at 7.5 and 37.5 cm. Obtaining this set of soil samples was complicated by the compressibility and stickiness of the wet surface soil caused by rainfall on the night of 12 August and the morning of 13 August. It was difficult to ascertain the actual depth that the soil samples represented, and it is certainly possible that the soil samples represented shallower and wetter soil than intended. If so, then this set of samples would act to falsely lower the slope of the
DPHP vs.
SS regression. The three sets of questionable soil samples mentioned above are identified by open symbols in Fig. 4. Removing these samples from the analysis leads to a slope of 0.97 for the regression of
DPHP vs.
SS at both depths. This is a significant improvement and indicates that errors in
SS could be largely responsible for the lower-than-expected slope.
Errors in the measurement of q or
Tm are a second potential contributor to the lower-than-expected slope of
DPHP vs.
SS. If q were consistently underestimated or overestimated by some fixed percentage or by some constant value, then the error would have been automatically accounted for during sensor calibration, and it would not affect
DPHP. The same holds true for a fixed percentage-wise error in
Tm. The only foreseeable way in which either of these measurement errors could cause the slope of the
DPHP vs.
SS to be <1 would be if
Tm were consistently underestimated by some constant value. This seems unlikely.
Violations of the assumptions behind the DPHP technique are the third potential contributor to the lower-than-expected slope of the
DPHP vs.
SS relationship. Some of the assumptions behind Eq. [3] have been investigated carefully. Kluitenberg et al. (1993) investigated the effects of the assumptions that the heat transfer around the DPHP sensor is the same as the heat transfer around an infinite line source and that the finite duration heat pulse approximates an instantaneous heat pulse. They reported that for the sensor geometry and heating time used here, estimates of C obtained by Eq. [1] are within 1% of the estimates obtained by use of more rigorous models. The assumption that heat transfer occurs only by conduction has been investigated by Bilskie (1994) using a numerical model for conduction and convection heat transfer around a heat-pulse sensor. He concluded that under typical conditions, convection has no effect on
T at points more than 2 mm from the heater.
In applying Eq. [3], we assumed that
b did not change with time; however, it is possible that
b could change with time in conventionally tilled plots like the ones used in this study. If
b changed with time at the measurement depths in our plots, then the difference between
DPHP and
SS should have changed with time also. Instead, the data show that
DPHP was greater than
SS by a fairly consistent amount throughout the study (Fig. 3), so change in
b with time cannot adequately explain the data. It is worthwhile to note that any error in
b would effect both
DPHP and
SS. For example, if the true
b were 0.1 Mg m-3 greater than the
b value used in Eq. [3], then water content estimated by a DPHP sensor would contain a +0.018 m3 m-3 error. The same 0.1 Mg m-3 error in
b would cause a -0.020 m3 m-3 error in
determined by soil sampling if the gravimetric water content of the soil were 0.20 kg kg-1. Then, the difference between the water contents determined with these two methods would be +0.038 m3 m-3, and the apparent error of the DPHP technique would be greater than the true error.
The effects of the remaining assumptions listed immediately following Eq. [3] are currently unknown, and one or more of these assumptions could contribute to the unexpectedly low slope of the
DPHP and
SS relationship. Additionally, the assumption employed in sensor calibration that agar-stabilized water has the same heat capacity as pure water is untested and could potentially influence the slope of the
DPHP and
SS relationship. Underestimating the heat capacity of the agar-stabilized water would lead to overestimating the needle spacing. Overestimating the needle spacing would result in a lower-than-expected slope for the
DPHP and
SS relationship.
Matching Point Procedure
Previous research has indicated that the DPHP technique excels in determining 
(Tarara and Ham, 1997). On the basis of this knowledge, we chose to apply a matching point procedure to adjust the
DPHP data. We shifted all the water content data for each sensor up or down by a constant value to make the first water content measurement from each sensor equal the water content determined from soil sampling near that sensor at the time of installation. The resulting time series graphs shown in Fig. 5 demonstrate that this matching point procedure improved the accuracy of
DPHP. The bias was not totally eliminated by use of the matching point procedure, but the absolute value of the bias was decreased. After applying the matching point procedure,
DPHP was, on average, 0.022 m3 m-3 <
SS at the 7.5-cm depth. At the 37.5-cm depth,
DPHP was on average 0.025 m3 m-3 <
SS. As mentioned previously, some evaporation likely occurred from the initial set of soil samples that were used in the matching point procedure. If evaporation did occur, it could explain the observation that subsequent
DPHP values tended to be lower than
SS values. The maximum absolute difference between
DPHP and
SS was 0.047 m3 m-3 at the 7.5-cm depth and 0.046 m3 m-3 at the 37.5-cm depth. At both depths, the maximum absolute difference occurred on 13 August, which is when the maximum value of
SS was recorded. The temporal trend of
DPHP is unaltered by the matching point procedure.
|
SS and
DPHP after the application of the matching point procedure is shown in Fig. 6. The r2, RMSE, and slope of the linear regressions of
DPHP vs.
SS are unchanged from those in Fig. 4, but the intercepts of the regression lines are reduced from about 0.1 to about 0.05. The vertical error bars in Fig. 6 highlight the reduced variability among sensors, which is the main benefit obtained by applying the matching point procedure. Notice that the vertical error bars in Fig. 6 are much shorter than those in Fig. 4. Applying the matching point procedure markedly reduced the variability among the DPHP sensors. Without the matching point procedure, the average SD of water content determined by the sensors was 0.063 m3 m-3; after applying the matching point procedure, the average SD of water content determined by the sensors was 0.026 m3 m-3. This is similar to the average SD for water content determined by soil sampling which was 0.022 m3 m-3. It is reasonable to attribute most of the remaining variability between DPHP sensors to real spatial variability of
in the root zone. The matching point procedure appears to be a simple method to obtain improved agreement between multiple DPHP sensors in the field. Such agreement among sensors is particularly important in applications where relative differences in
between different spatial locations are of primary interest. Note that applying the matching point procedure requires no soil sampling beyond that which is normally required to use the DPHP technique. (To use Eq. [3], one must obtain soil samples to determine
b.)
|
| CONCLUSION |
|---|
|
|
|---|
with high temporal and spatial resolution. The response of the DPHP sensors was linear, and the precision was excellent with RMSE values around 0.01 m3 m-3. For this soil, linear regression of
DPHP vs.
SS yields a slope of 0.75 rather than 1. This differs from the results of others who have found the slope of this relationship to be between 0.86 and 0.94, but it seems probable that errors in
SS contributed to the low slope in this study. In any case, the strong linearity of the relationship will be conducive to determining soil-specific calibrations if necessary. A matching-point procedure we adopted improved the accuracy of the technique and improved the agreement between multiple DPHP sensors in the field. | ACKNOWLEDGMENTS |
|---|
| REFERENCES |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
T. E. Ochsner and J. M. Baker In Situ Monitoring of Soil Thermal Properties and Heat Flux during Freezing and Thawing Soil Sci. Soc. Am. J., July 1, 2008; 72(4): 1025 - 1032. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. H. Young, G. S. Campbell, and J. Yin Correcting Dual-Probe Heat-Pulse Readings for Changes in Ambient Temperature Vadose Zone J., January 23, 2008; 7(1): 22 - 30. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. M. DeSutter, T. J. Sauer, T. B. Parkin, and J. L. Heitman A Subsurface, Closed-Loop System for Soil Carbon Dioxide and Its Application to the Gradient Efflux Approach Soil Sci. Soc. Am. J., January 11, 2008; 72(1): 126 - 134. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. H. Knight, W. Jin, and G. J. Kluitenberg Sensitivity of the Dual-Probe Heat-Pulse Method to Spatial Variations in Heat Capacity and Water Content Vadose Zone J., October 8, 2007; 6(4): 746 - 758. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Heitman, R. Horton, T. Ren, and T. E. Ochsner An Improved Approach for Measurement of Coupled Heat and Water Transfer in Soil Cells Soil Sci. Soc. Am. J., May 16, 2007; 71(3): 872 - 880. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. E. Ochsner, T. J. Sauer, and R. Horton Soil Heat Storage Measurements in Energy Balance Studies Agron. J., January 1, 2007; 99(1): 311 - 319. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. E. Ochsner, T. J. Sauer, and R. Horton Field Tests of the Soil Heat Flux Plate Method and Some Alternatives Agron. J., June 5, 2006; 98(4): 1005 - 1014. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Ren, Z. Ju, Y. Gong, and R. Horton Comparing Heat-Pulse and Time Domain Reflectometry Soil Water Contents from Thermo-Time Domain Reflectometry Probes Vadose Zone J., November 11, 2005; 4(4): 1080 - 1086. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. E. Ochsner, R. Horton, G. J. Kluitenberg, and Q. Wang Evaluation of the Heat Pulse Ratio Method for Measuring Soil Water Flux Soil Sci. Soc. Am. J., May 6, 2005; 69(3): 757 - 765. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Mori, J. W. Hopmans, A. P. Mortensen, and G. J. Kluitenberg Estimation of Vadose Zone Water Flux from Multi-Functional Heat Pulse Probe Measurements Soil Sci. Soc. Am. J., April 11, 2005; 69(3): 599 - 606. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Ham and E. J. Benson On the Construction and Calibration of Dual-Probe Heat Capacity Sensors Soil Sci. Soc. Am. J., July 1, 2004; 68(4): 1185 - 1190. [Abstract] [Full Text] [PDF] |
||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||