Tree Physiology 24, 1323–1331 © 2004 Heron Publishing—Victoria, Canada Detection of tree roots and determination of root diameters by ground penetrating radar under optimal conditions† CRAIG V. M. BARTON1,2 and KELVIN D. MONTAGU1 1 Forest Research and Development Division, State Forests of NSW, P.O. Box 100, Beecroft, NSW 2119, Australia 2 Corresponding author ([email protected]) Received December 10, 2003; accepted February 20, 2004; published online October 1, 2004 Summary A tree’s root system accounts for between 10 and 65% of its total biomass, yet our understanding of the factors that cause this proportion to vary is limited because of the difficulty encountered when studying tree root systems. There is a need to develop new sampling and measuring techniques for tree root systems. Ground penetrating radar (GPR) offers the potential for direct nondestructive measurements of tree root biomass and root distributions to be made. We tested the ability of GPR, with 500 MHz, 800 MHz and 1 GHz antennas, to detect tree roots and determine root size by burying roots in a 32 m 3 pit containing damp sand. Within this test bed, tree roots were buried in two configurations: (1) roots of various diameters (1–10 cm) were buried at a single depth (50 cm); and (2) roots of similar diameter (about 5 cm) were buried at various depths (15–155 cm). Radar antennas were drawn along transects perpendicular to the buried roots. Radar profile normalization, filtration and migration were undertaken based on standard algorithms. All antennas produced characteristic reflection hyperbolas on the radar profiles allowing visual identification of most root locations. The 800 MHz antenna resulted in the clearest radar profiles. An unsupervised, maximum-convexity migration algorithm was used to focus information contained in the hyperbolas back to a point. This resulted in a significant gain in clarity with roots appearing as discrete shapes, thereby reducing confusion due to overlapping of hyperbolas when many roots are detected. More importantly, parameters extracted from the resultant waveform through the center of a root correlated well with root diameter for the 500 MHz antenna, but not for the other two antennas. A multiple regression model based on the extracted parameters was calibrated on half of the data (R 2 = 0.89) and produced good predictions when tested on the remaining data. Root diameters were predicted with a root mean squared error of 0.6 cm, allowing detection and quantification of roots as small as 1 cm in diameter. An advantage of this processing technique is that it produces results independently of signal strength. These waveform parameters represent a major advance in the processing of GPR profiles for estimating root diameters. We conclude that enhanced data analysis routines combined with improvements in GPR hardware design could make GPR a valuable tool for studying tree root systems. Keywords: GPR, nondestructive root measurement, radar antenna, root biomass. Introduction Roots account for between 10 and 65% of a tree’s total biomass, depending on factors such as age, species, water and nutrient availability, and competition (see reviews by Vogt et al. 1996, Cairns et al. 1997, Keith et al. 2000, Snowdon et al. 2000). However, such reviews also highlight the limited understanding we have of tree root systems. Worldwide interest in carbon sequestration by reforestation and afforestation has led to increased research on tree root biomass and an increased demand for accurate methods of estimating belowground biomass stocks (Watson et al. 2000). Furthermore, to refine forest process-models, a greater understanding of the fate of carbon allocated to tree root systems is required; however, sampling tree roots, particularly of larger trees, presents logistical difficulties. Common techniques are limited to combinations of excavation and coring (e.g., Burrows et al. 2000, Resh et al. 2003, Ritson and Sochacki 2003), both of which are destructive, costly, time consuming and laborious. A nondestructive sampling technique would, therefore, be of value. For years, geophysicists have detected features in sub-surface rock with ground penetrating radar (GPR). More recently, GPR has been used to detect buried pipes, abandoned storage tanks, artifacts, disturbed soil, caves and land mines. Ground penetrating radar has also been used to detect tree roots and map root systems (Hruska et al. 1999, Sustek et al. 1999, Èermák et al. 2000, Wielopolski et al. 2000) and to determine root biomass (Butnor et al. 2001, 2003). However, both the measurement and data processing techniques need considerable refinement before GPR can be widely employed to measure tree root biomass. Principles of ground penetrating radar Ground penetrating radar generates a series of broadband electromagnetic pulses that are directed into the ground from a specially oriented antenna. As the pulse travels through the ground, it is reflected, deflected and absorbed to varying degrees by the materials (soil, water, rocks, roots) through which † This paper was among those presented at the third meeting of the International Union of Forest Research Organizations concerning “Dynamics of physiological processes in woody roots,” convened by the School of Plant Biology, University of Western Australia, Crawley, WA. 1324 BARTON AND MONTAGU it travels. It is the contrast in the dielectric permittivity between the bulk medium and buried objects that causes reflections: the greater the difference in dielectric permittivity, the greater the coefficient of reflectivity (Conyers and Goodman 1997). A receiver in the antenna picks up the return signal and the radar control unit records the two-way travel time, amplitude and polarity of the return signal. This information is typically plotted on a vertical scale with time on the ordinate and signal strength and polarity on the abscissa, and is referred to as an A-scan or trace. When operating, the antenna is dragged across the ground along a transect and it fires a pulse at regular intervals of either time or position. Multiple traces are then combined to form a typical GPR profile scan (B-scan), with distance on the abscissa and two-way travel time of signal on the ordinate, with a grey or false color scale used to represent the intensity and polarity of the return signal. The pulse emitted from the antenna has an elliptical cone of divergence and scans a footprint area beneath it, with the long axis of the elliptical cone in the direction of travel (Conyers and Goodman 1997). As the antenna is dragged across the surface, the travel-time for a return signal from a buried object decreases to a minimum when the antenna is directly above the object then increases again as the antenna moves away from the object, this results in a characteristic hyperbola in the radar profile. The clearest hyperbolas are formed by point objects or by linear objects with the major axis horizontal and normal to the direction of travel of the antenna. Linear objects with the major axis in the direction of travel of the antenna produce linear features on the radar profile but do not produce hyperbolas, whereas other interception angles produce distorted hyperbolas. The central frequency of the radar unit influences the size of the footprint, with higher frequencies resulting in a smaller, more focused footprint (Conyers and Goodman 1997). The central frequency also influences the depth of penetration and the resolution of the system. Higher frequencies are attenuated more rapidly, such that a 100 MHz system will provide information to around 30-m depth, whereas a 2-GHz system is unlikely to provide useful information beyond about 0.2 m. Typical maximum depths of penetration rarely exceed 20 wavelengths, except in a low attenuation, dielectric medium (Daniels 1996). The attenuation depends on the magnetic permeability and electrical conductivity of the medium. In soil, water content and mineralogy have a large impact, with high water, clay and salt contents attenuating the signal most strongly. Under unfavorable conditions of wet, calcareous or clay rich soils, the maximum depth of GPR penetration can be < 1 m, regardless of the frequency of antenna used (Conyers and Goodman 1997). Higher frequency systems with their shorter wavelengths have higher resolution (i.e., the ability to detect small objects and to discriminate between closely spaced objects). Thus a compromise between penetration and resolution must be made and it is an important consideration in the selection of system frequency. The aim of our study was to determine if GPR could detect tree roots and measure root diameter under the optimal condi- tions of a sand test-bed. We tested the ability of three antennas of different frequencies to detect roots of various sizes and at various depths. We also describe a data analysis method that gives more accurate estimates of root diameter than previously published methods. Materials and methods Site To create optimal testing conditions, we chose damp sand as the test medium because it has a permittivity similar to soil but is homogeneous with uniform bulk density and no structure or voids that will interact with the radar pulse. The sandpit, 4 × 4 m square and 2 m deep, was cut into the side of a steep slope. Wooden walls were lined with polyethylene to prevent lateral flow of water into the pit from the neighboring soil. The front wall of the pit had a large opening to facilitate emptying. The pit was filled with 50 Mg of washed, coarse river sand (< 3 mm). To avoid edge effects, only the central 2 × 2 × 1.5 m volume was used as the working area for root burial. Roots Roots were obtained from a forestry felling operation in the Hunter region (NSW). Native hardwood (Eucalyptus sp.) tree stumps were excavated with a mechanical harvester and a selection of roots was taken to the laboratory for grading. Sections of root, circular in cross section, roughly straight with minimal taper and 50 cm long, were chosen. The cut ends were sealed with molten wax to minimize water loss. Subsamples of each root were taken to determine wood density (about 0.63 g cm –3) and water content (about 65% gravimetric). Two orthogonal diameters were measured at 10-cm intervals along the length of each root and the mean diameter calculated. The working area of the sandpit was divided in half and two trials were simultaneously undertaken. In the first half, nine roots of various diameters (1–10 cm) were buried at a depth of 50 cm, and in the second half, eight roots of similar diameter (about 5 cm) were buried at depths of 15 to 155 cm. All roots were buried parallel to one another so that the GPR transects would pass normal to the root axis (see Figure 1) thus avoiding the complication of distorted hyperbolas that would arise if the antenna tracked across the root at shallow angles. The horizontal distance between roots was 25 cm for roots buried at one depth and 31 cm for roots buried at different depths. A further five roots were buried at 155-cm depth beneath the trials to assess the effect of stacking on the ability of GPR to detect and size roots. Data collection The sandpit was allowed to settle for 4 weeks after filling before the radar was tested. A field-portable GPR system (RAMAC/GPR, Malå Geosciences, Malå, Sweden) with three antennas (500 MHz, 800 MHz and 1 GHz) was used. Thirteen transects 15 cm apart, perpendicular to the long axis of the roots were established (see Figure 1). Radar profiles were collected along these transects with each of the three antennas. TREE PHYSIOLOGY VOLUME 24, 2004 MEASURING TREE ROOTS USING GPR The RAMAC GPR antennas each have a small measuring wheel that enables their position along a transect to be determined accurately. The measuring wheel of the 1 GHz antenna was very small, so to prevent it from digging into the sand and dragging rather than rotating, a sheet of polyethylene was laid across the sand pit. Each profile consisted of between 294 and 315 traces (horizontal resolution = 0.95 cm) and each trace had 511 samples (vertical time step = 0.08–0.09 ns). Four transects passed directly over the roots buried at 50 cm (Transects 2–5) and four transects passed directly over the roots buried at various depths (Transects 9–12). The other five transects passed either to the side of or between the two strips of buried roots and enabled determination of the information contained in the radar side-look. Data processing Radar profile normalization, filtration and migration routines were performed with MathCad 2000 (MathSoft, Cambridge, MA). The main features of interest in the radar profiles were the hyperbolas, which indicated a root or other point feature buried in the sandpit. Several data pre-processing algorithms were applied in a stepwise fashion to remove background noise and improve identification of the hyperbolas. First, application of a background removal filter removed the parallel bands observed in the scans, which result from plane reflectors such as the ground surface, soil horizons and bands of low frequency noise. Second, removal of the DC offset and DC drift compensated for any slight drift in the zero in each trace that make up the full profile (Daniels 1996). Third, application of a 5 × 5 median gradient filter smoothed out any random noise (Pratt 1991, Olhoeft 2000). This filter acted as a low-pass filter both along the transect and through time, suppressing trace and time-dependent noise and spike events such as mobile phone interference. 1325 Following the pre-processing, the velocity of propagation of the signal through the sand was determined. The shape of a hyperbola depends on the velocity of propagation of the signal through the sand and the depth of the object. The deeper the object and the faster the propagation velocity, the flatter the hyperbola (Daniels 1996). A modeled hyperbola was overlayed on the profile and the velocity parameter adjusted until the simulated hyperbola matched the observed hyperbolas. Based on this approach, the propagation velocity was estimated to be 13.5 cm ns –1. An advantage of using damp sand is that the signal velocity is uniform throughout the sandpit. Because the strength of the return signal deteriorates exponentially with travel time, a combination of linear and exponential gain was applied to the profiles to enhance the visibility of hyperbolas and aid in the determination of propagation velocity. This gain was not used during the migration and parameter extraction described below. With the signal propagation velocity obtained previously, an unsupervised maximum-convexity migration algorithm was applied to each profile, focusing the information contained in the hyperbolas back to a point. This method assumes a semi-hyperbolic maximum-convexity function and sums the value of each separate trace at the point at which it intersects the semi-hyperbolic focus over the ensemble data set. All in-phase energy is additive, whereas non-coherent energy is usually out of phase and sums to zero (Daniels 1996). The algorithm is applied to every point in the GPR scan regardless of whether or not it is at the peak of a hyperbola. If the point is at the peak of a hyperbola, then all of the information contained in the hyperbola is focused to that point; if not, then it focuses random noise to that point that tends to sum to zero. This unsupervised approach does not require an operator to visually locate hyperbolas on the raw radar scan prior to processing. It automatically highlights point and line reflectors normal to the plane of the profile and removes the clutter associated with the constructive and destructive interference between hyperbolas. This results in discrete zones at the focal point of each hyperbola in the GPR profile. After application of the filters and migration algorithm, the location of the buried roots became evident and visual inspection of the migrated profiles indicated that there might be a relationship between the size of roots and the “wavelength” of the migrated trace through the root. To investigate this relationship further, the traces passing through the center of each root were selected for analysis and the times between successive zero crossings of the reflected waveform extracted (see Figure 5). The first four of these time intervals (referred to as parameters a–d) were correlated against root size for each of the antennas. Model fitting and testing Figure 1. The positions of roots buried in the sand pit (solid horizontal lines) and the transects along which the radar antennas were pulled (broken vertical lines). A multiple linear regression was performed to determine the best empirical model relating the extracted parameters (a–d) to root size. The first three parameters (a–c) explained most of the variation and were therefore used subsequently (see Figure 6). To test the data dependence of the model, half of the TREE PHYSIOLOGY ONLINE at http://heronpublishing.com 1326 BARTON AND MONTAGU data were used to calibrate the model, and the remaining data were used to test the model; i.e., data from two of the four transects scanning each of the two halves of the sandpit were used to calibrate the model (Transects 2, 4, 9 and 11), and the other four transects that passed directly over roots were used to test the model (Transects 3, 5, 10 and 12). Results After filtering the profiles, hyperbolas were observed for each of the roots of various diameters buried at 50-cm depth in scans of all three antennas (Figure 2). Hyperbolas were visible for all nine roots, although the hyperbola for the smallest root, the one furthest to the right, was faint. The hyperbolas for the 500 MHz system were the least sharply defined. For each antenna, at least one of the roots buried at 155-cm depth beneath the row of roots buried at 50-cm depth was visible. For the 500 and 800 MHz antennas, a second root at 50-cm depth was visible, although indistinct. Similar results were observed for the other three transects that ran directly above the roots buried at 50 cm and for roots buried at different depths (data not shown). The GPR profiles for roots of the same size buried at different depths showed a similar pattern, with more clearly defined hyperbolas obtained with the 800 MHz and 1 GHz antennas compared with the 500 MHz antenna (Figure 3). A common feature of all profiles was the interference between hyperbolas, making it difficult to determine their exact positions. This interference increased with decreasing antenna frequency. The GPR profile of transects that did not pass directly over roots contained weak hyperbolas indicating some degree of side- look; it was difficult to extract useful information from these transects and they were therefore excluded from further analysis. The effect of the migration algorithm is illustrated in Figure 4. Figures 4A and 4C show the filtered radar profiles (500 MHz) of transects directly over the roots, buried at various depths (same root diameter) or buried at one depth (varying root diameter) respectively. Figures 4B and 4D show the corresponding profiles after migration. The positions of most of the roots were clearer after applying the migration algorithm. The positions of the roots at various depths can be seen in Figure 4B. The migrated zones become fainter with depth as a result of signal attenuation, but the size of the zones appears relatively constant. In Figure 4D, the positions of the roots buried at 50 cm were clear and the size of the migrated zones appeared to vary with root size. Two of the roots buried at 155 cm were clearly visible, but the third root was undetectable, probably because it was too close to the side of the sand pit and as a result, only one leg of the hyperbola contained information. This also explains why the migrated “blob” for the rightmost root buried at 50 cm is less well defined than the others. The apparent size of the migrated zone is a function of the wavelength of the return wavelet (see Figure 5). Figure 5 shows a typical migrated zone using the 500 MHz antenna and the corresponding wavelet extracted from the trace through the center of the zone. Parameters a–d are the time intervals (in ns) between zero crossings of the waveform. It was fairly straightforward to extract the parameters for the 500 MHz profiles but more difficult for the 800 MHz profiles and very difficult for the 1 GHz profiles because of confused waveforms that some- Figure 2. Radar profiles from three antennas (500 MHz, 800 MHz, 1 GHz) along a transect across the center of nine roots of various sizes (1–10 cm diameter) buried 50 cm deep in the sand pit. Two of the three roots buried at 155 cm deep can be seen on the 500 MHz image and one root on the 800 MHz and 1 GHz images. Horizontal direction represents distance along the transect and vertical direction represents the travel time of the signal. TREE PHYSIOLOGY VOLUME 24, 2004 MEASURING TREE ROOTS USING GPR 1327 Figure 3. Radar profiles from three antennas (500 MHz, 800 MHz, 1 GHz) along a transect across the center of eight roots of similar size (5 cm diameter) buried in the sand pit at depths of 15–155 cm. Figure 4. (A) Radar profile from the 500 MHz antenna along a transect across the center of eight roots of the similar diameter (5 cm) buried at various depths (15–155 cm). The characteristic hyperbolas are overlapping and interfering with each other, making interpretation impossible. (B) Eight roots clearly visible after the radar profile in (A) had been processed with the migration algorithm. (C) Radar profile along a transect across the center of nine roots of various sizes buried 50 cm deep. (D) Nine roots are clearly visible after the radar profile in (B) had been processed with the migration algorithm. Again the position of the roots is obvious. The arrows in (D) indicate the two roots buried at 155 cm. TREE PHYSIOLOGY ONLINE at http://heronpublishing.com 1328 BARTON AND MONTAGU Figure 5. (A) Close up of a processed 500 MHz profile showing two roots. (B) Trace through the center of the first root as indicated by the vertical line in (A). Parameters a–e are determined from the trace as the time (ns) between zero crossings of the waveform. times failed to cross the zero line. There was a positive correlation between root size and parameters a–d for the 500 MHz antenna (Figure 6), which was especially strong for parameters b and c. Similar plots for the 800 MHz and 1 GHz antennas failed to show such correlations (data not shown) and so no further analysis using data from these antennae was performed. The model fitted to half of the data for the 500 MHz antenna is shown in Figure 7. The coefficient of determination was 0.89 and the root mean squared error (RMSE) was 0.51 cm. The fitted model was used to predict root diameters for the other half of the data set (Figure 8). The residuals indicate that the model generally performed well, with a slight bias toward over estimating root size. The RMSE of 0.56 cm indicates that the size of individual roots could be estimated fairly accurately. Discussion Investigation of tree root systems with GPR has been largely confined to qualitative mapping (Hruska et al. 1999, Èermák et al. 2000). Attempts to quantify tree root systems have met with mixed success (Butnor et al. 2001, 2003). Butnor et al. (2003) found reasonable correlation between root biomass in the top 30 cm of forest soil in soil cores and information obtained from GPR. Under ideal conditions, we were able to locate buried roots and extract information from a processed waveform that correlated well with root diameter (Figure 7). When several closely spaced targets exist, such as tree root systems, GPR profiles usually produce a confusing profile because of interactions between the hyperbolas from each target. This is readily illustrated by the profiles in Figure 2, even after normalization and filtering. However, visual identification of hyperbolas associated with the tree roots was possible for all Figure 6. Relationships between waveform parameters a–d (ns) and root diameter (cm) for all eight transects using the 500 MHz antenna. The circles show roots of varying sizes (1–8 cm diameter) buried at one depth (50 cm), whereas the triangles show roots of similar size (5 cm diameter) buried at various depths (15–155 cm). TREE PHYSIOLOGY VOLUME 24, 2004 MEASURING TREE ROOTS USING GPR Figure 7. Fitted model relating mean root diameter to parameters extracted from processed GPR data. The model was fitted to one half of the complete data set. The circles denote roots of various sizes buried at 50 cm and the triangles denote roots of similar size buried at different depths (15–155 cm). The broken line is the 1:1 relationship. The fitted model is: diameter = –17.1527 + 0.3066a + 1.31b + 0.70c – 0.032b2 – 0.0014abc, r 2 = 0.89, RMSE = 0.5. See Figure 5 for definitions of parameters a, b and c. three GPR antennas for most roots down to a depth of 155 cm and between 1–10 cm in diameter. Even when roots were buried below other roots, the three systems tested were able to detect the deeper buried roots. The depth of penetration of the 1 GHz antenna was better than expected, given that the higher the central frequency and the shorter the wavelength, the more quickly the signal is attenuated. Low frequency antennas (10–120 MHz) generate long wavelength radar energy that can penetrate up to 50 m under certain conditions, but the maximum depth penetration of a 1 GHz antenna is about 1 m or less in typical soils (Conyers and Goodman 1997). The depth of penetration of the 1 GHz antenna in our study reflects the low attenuation properties of the damp sand used in the test bed. Under field conditions, with typically higher soil water 1329 and clay content, such depth of penetration would be unlikely. In terms of simple visual identification of hyperbolas, the 800 MHz antenna gave the clearest radar profiles and appears to represent a good balance between resolution and depth of penetration for field surveys. To overcome confusing GPR profiles and hence improve the visual identification of root location, we applied an unsupervised maximum-convexity migration algorithm (Daniels 1996). This resulted in a significant gain in clarity with the roots appearing as discrete shapes (Figure 4). The use of the migration algorithm was simplified by the uniform propagation velocity throughout the sand medium. It would be expected that, for tree roots, velocity would vary because of variations in soil water content and composition down the profile. However, more complex migration algorithms exist that allow for variations in propagation velocity within the measurement volume (Daniels 1996). Thus, it appears that a migrating algorithm could be applied to data from roots in situ. We have discussed improved methods for processing GPR data to assist in the visual identification of root location and root mapping as used by Hruska et al. (1999). However, if GPR is to find wide application in tree root studies, techniques that allow the size of roots to be determined and their biomass to be estimated are required. Few attempts have been made to extract quantitative information on tree root systems from GPR data. Butnor et al. (2001) used signal intensity to obtain information on root diameter and biomass under field conditions. Roots of known size were buried at 15 and 30 cm and a correlation was observed between return signal strength and root diameter that deteriorated rapidly with depth (r = 0.81 to 0.55 at 15- and 30-cm depths, respectively). Butnor et al. (2001) also scanned several forested areas with GPR and then excavated roots and looked at the correlation between total root biomass and a measure of return signal energy; however, the correlations were weak (r = 0.34 to 0.57), because of the many confounding influences on signal strength (e.g., depth, angle of crossing and dielectric properties of the medium). Butnor et al. (2003) employed a slightly different approach with better results under field conditions. They applied a hori- Figure 8. Model testing: the predicted values of root diameter, using the half of the data not used to fit the model, plotted against the actual mean root diameters. The residual plots show that residuals are normally distributed with a slight positive bias (0.2 cm) and RMSE = 0.56 cm. TREE PHYSIOLOGY ONLINE at http://heronpublishing.com 1330 BARTON AND MONTAGU zontal distance normalization filter, a background removal filter, followed by a Hilbert transformation to the raw GPR scans along transects and then estimated the number of pixels above a threshold. After adjusting for different relationships between fertilized and unfertilized plots, the resulting pixel count was correlated (r = 0.86) with the root biomass in soil cores taken at intervals along the transects. We also examined the use of signal strength and found it to be poorly correlated with root size, primarily because of attenuation of the signal with depth. Consequently, we conclude that it is unlikely that quantitative information on root size can be obtained from signal strength because of the large number of confounding influences that need to be taken into account. The major finding of our study was that root diameter could be estimated from the waveform parameters of migrated hyperbola from the 500 MHz antenna (Figures 5–7). Our model provided good predictions of actual root diameter ranging from 1 to 8 cm (Figure 8). A major advantage of the processing technique is that it produces results that are independent of signal strength. Thus, the diameters of roots buried at different depths could be estimated with no corrections for depth, because the waveform parameters used in the model (measured time between zero crossings; Figure 5b) were unaffected by depth for roots buried at depths of 15 to 155 cm deep. In contrast, strength of the signal varied considerably as shown in Figure 4B where the visibility of the same diameter roots decreases with depth. The use of waveform parameters represents a major advance in the processing of GPR profiles for the study of tree root systems. The roots used in our study were not perfect cylinders and the diameters reported are actually the mean diameter of orthogonal measurements at 10-cm intervals along the root. There was some variation in diameter and non-circularity in cross section with the mean coefficient of variation of diameter along a root being 10%. Therefore some of the variation in the model fit will be a result of this variation in diameter along the root. From theory, we expected the higher frequency antennas, with their shorter wavelength and higher resolution, to provide the most information about root diameter. However, it was extremely difficult to extract information that correlated with root size from the migrated traces from either the 1 GHz or 800 MHz antenna. There may be useful information in these data, in which case the approach we adopted may be inappropriate for those frequencies. The relationship we derived between the waveform parameters from the 500 MHz system and root diameter is purely empirical and the underlying physical principles are not fully understood. Improved algorithms designed for complex forest ecosystems could possibly be developed in partnership between biologists and those with more expertise in the relevant field of physics. However, even without a full understanding of the physics, our approach provides a useable method of nondestructively determining root diameter with a reasonable degree of precision and accuracy, particularly given that the 500 MHz antenna has good depth penetration under a wide range of field conditions. Variation in soil water content over time or from site to site will influence the signal attenuation and propagation velocity and consequently the strength of the return signal. This would have implications for algorithms that rely on signal strength to relate biomass to GPR data (e.g., Butnor et al. 2001, 2003); however, it is uncertain how such variation in water content would influence the parameters extracted from the return signal used in this study. More work is required to determine if the waveform parameter approach can be adapted for use under field conditions. This study was conducted under optimum conditions with a uniform medium, roots widely spaced and not overlapping, and the antenna tracked at 90 degrees to the roots. Under field conditions, roots grow at varying angles, varying depths, often in clumps, and in a heterogeneous medium, resulting in more complex radar images. We did not assess the impact of the antenna crossing the root at angles other than 90° as would occur in the real world, but it is likely that the relationship between the parameters we have extracted and root size would break down under such conditions. Improvements in antenna design by using stepped frequency (Jensen and Gregersen 2000), cross polarization and steerable beams (Utsi 2000) combined with optimized survey grids and data analysis routines could advance the use of GPR for tree root studies. By running transects close to one another and at a range of angles across a plot a vast amount of information would be obtained that could be analyzed with the type of algorithms currently used in medical scanners to yield information on root architecture and biomass. Given the absence of other techniques, apart from excavation, for measuring tree root systems, further study of GPR for studying tree root systems seems worthwhile. Acknowledgments We thank Tim Pippett of Alpha Geoscience Pty. for his assistance collecting the GPR data. This study was funded under program A2 of the CRC for Greenhouse Accounting. References Burrows, W.H., M.B. Hoffmann, J.F. Compton, P.V. Back and L.J. Tait. 2000. 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