The flow of electric current in the root-soil system relates to the pathways of water and solutes, its characterization provides information on the root architecture and functioning. We developed a current source density approach with the goal of non-invasively image the current pathways in the root-soil system.
A current flow is applied from the plant stem to the soil, the proposed geoelectrical approach images the resulting distribution and intensity of the electric current in the root-soil system. The numerical inversion procedure underlying the approach was tested in numerical simulations and laboratory experiments with artificial metallic roots. We validated the method using rhizotron laboratory experiments on maize and cotton plants.
Results from numerical and laboratory tests showed that our inversion approach was capable of imaging root-like distributions of the current source. In maize and cotton, roots acted as “leaky conductors”, resulting in successful imaging of the root crowns and negligible contribution of distal roots to the current flow. In contrast, the electrical insulating behavior of the cotton stems in dry soil supports the hypothesis that suberin layers can affect the mobility of ions and water.
The proposed approach with rhizotrons studies provides the first direct and concurrent characterization of the root-soil current pathways and their relationship with root functioning and architecture. This approach fills a major gap toward non-destructive imaging of roots in their natural soil environment.
New root phenotyping technological developments are needed to overcome the limitations of traditional destructive root investigation methods, such as soil coring or “shovelomics” (Trachsel et al. 2011). Mancuso (2012) and Atkinson et al. (2019) provide extensive reviews on the methodological advances on non-destructive root phenotyping, including Bioelectrical Impedance Analysis (BIA), planar optodes, geophysical methods, and vibrating probe techniques. These techniques aim to mitigate key limitations of traditional root phenotyping, especially addressing the need for a better and more convenient characterization of the finer roots and root functioning. Advances in non-invasive and in-situ approaches for monitoring of root growth and function over time are needed to gain insight into the mechanisms underlying root development and response to environmental stressors.
Geophysical methods have been tested to non-destructively image roots in the field. Ground Penetrating Radar (GPR) approaches have been used to detect coarse roots (Guo et al. 2013; Liu et al. 2018). Electrical Resistivity Tomography (ERT) and ElectroMagnetic Induction (EMI) approaches have been used to image and monitor soil resistivity changes associated with the Root Water Uptake (RWU) (Cassiani et al. 2015; Shanahan et al. 2015; Whalley et al. 2017). Recent studies explored the use of multi-frequency Electrical Impedance Tomography (EIT) to take advantage of the root polarizable nature (Weigand and Kemna 2017, 2019).
Despite these advantages, geophysical methods to date share common limitations regarding root characterization. Geophysical methods developed to investigate geological media: in the case of roots they measure the root response as part of the soil response, see Fig. 1a for the ERT acquisition. Because of the natural soil heterogeneity and variability the resolution and signal characteristics of geophysical methods strongly depend on soil type and conditions. As such, interpretation of the root-soil system response is non-unique, hindering the differentiation between roots of close plants and the extraction of specific information about root physiology from the electrical signals.
Unlike geophysical methods, the BIA for root investigation developed to specifically target the impedance of plant tissues, limiting the influence of the growing medium. A practical consequence is that BIA involves the application of sensors (i.e., electrodes) into the plant to enhance the method sensitivity. BIA measures the electrical impedance response of roots at a single frequency (resistance and capacitance methods) or over a range of frequencies (bioelectrical impedance spectroscopy). The measured BIA responses have been used to estimate root characteristics, such as root absorbing area and root mass (Dietrich et al. 2012; Mancuso 2012; Ozier-Lafontaine and Bajazet 2005). Estimation of these root traits is based on assumptions on the electrical properties of roots (see section Current Pathways in Roots). A key assumption is that current travels and distributes throughout the root system before exiting to the soil (Fig. 1b), with no leakage of current into the soil in the proximal root position (Fig. 1c). It is only in the former case, that the BIA signal would be sensitive to root physiology. Despite the physiological relevance of the BIA assumptions and the number of BIA studies, a suitable solution for the characterization of the current pathways in roots is missing. Thus far, only indirect information obtained from invasive and time-consuming experiments have been available to address this issue (e.g., excavation and trimming).
Mary et al. (2018, 2019), and Mary et al. 2020) tested the combined use of ERT and Mise A La Masse (MALM) methods for imaging grapevine and citrus roots in the field. An approach hereafter called inversion of Current Source Density (iCSD) was used to invert the acquired data. The objective of this inversion approach is to image the density and position of current passing from the plant to the soil. The current source introduced via the stem distributes into “excited” roots that act as a distributed network of current sources (Fig. 1d). Consequently, a spatial numerical inversion of these distributed electric sources provides direct information about the root current pathways and the position of the roots involved in the uptake of water and solutes. The numerical approach used to invert for the current source density is a key component required for such an approach. Mary et al. (2018) used a nonlinear minimization algorithm for the inversion of the current source density. The algorithm consisted of gradient-based sequential quadratic programming iterative minimization of the objective functions (L1/L2 approach therein) described in Mary et al. (2018). The algorithm was implemented in MATLAB, R2016b, using the fmincon method. Because no information about the investigated roots was available, the authors based these inversion assumptions and the interpretation of their results on the available literature data on grapevine root architecture. Consequently, Mary et al. (2018) highlighted the need for further iCSD advances and more controlled studies on the actual relationships between current flow and root architecture.
In this study, we present the methodological formulation and evaluation of the iCSD method, and discuss its applications for in-situ characterization of current pathways in roots. We perform our studies using laboratory rhizotron experiments on crop roots. The main goals of this study were: 1) develop and test an iCSD inversion code that does not rely on prior assumptions on root architecture and function; 2) design and conduct rhizotron experiments that enable an optimal combination of root visualization and iCSD investigation of the current pathways in roots to provide direct insight on the root electrical behavior and validate the iCSD approach; and 3) perform experiments to evaluate the application of the iCSD method on different plant species (maize and cotton) and growing medium (soil and nutrient solution) that are common to BIA and other plant studies.
Current pathways in roots
The relationship between hydraulic and electrical pathways has been the object of scientific debate because of its physiological relevance and methodological implications for BIA methods (Urban et al. 2011; Dietrich et al. 2012). A key and open question concerns the distribution of the current leakage (i.e., the root portions where the current passes from the root to the soil; Fig. 1b and c). The distribution of the current leakage is controlled by 1) the electrical radial and longitudinal conductivities (σcr and σcl), and 2) by the resistivity contrast between root and soil.
With regard to σcr and σcl, when σcl is significantly higher than σcr, the current will predominantly travel through the xylems to the distal “active” roots, which are mostly root hairs. Based on the link between hydraulic and electrical pathways, this is consistent with a root water uptake (RWU) process where root hairs play a dominant role while the more insulated and suberized roots primarily function as conduits for both water and electric current (Aroca 2012, and references therein). On the contrary, if the σcr is similar to σcl, the electrical current does not tend to travel through the entire root system but rather starts leaking into the surrounding medium from root proximal portions. The coexistence of proximal and distal current leakage is in line with studies that suggest the presence of a more diffused zone of RWU, and a more complex and partial insulation effect of the suberization, possibly resulting from the contribution of the cell-to-cell pathways (e.g., Kramer 1946; Steudle 2000; North and Baker 2007; Ranathunge and Schreiber 2011; Schreiber 2010).
Soil resistivity can affect the distribution of the current leakage by influencing the minimum resistance pathways, i.e., whether roots or soil provide the minimum resistance to the current flow. In addition, soil resistivity strongly relates to the soil water content, which, as discussed, affects the root physiology. Therefore, information on the soil resistivity, such as the ERT resistivity imaging, has the potential for supporting the interpretation of both BIA and iCSD results.
Dalton (1995) proposed a model for the interpretation of the plant root capacitance results in which the current equally distributes over the root system. Because of the elongated root geometry this model is coherent with the hypothesis of a low resistance xylem pathway (σcl > σcr). Numerous studies have applied Dalton’s model documenting the predicted correlation between root capacitance and mass (Dietrich et al. 2012, and references therein). In fact, recent studies with wheat, soy, and maize roots continue to support the capacitance method (Čermák et al. 2013; Preston et al. 2004; Postic and Doussan 2016; Cseresnyés et al. 2018).
Despite accumulating studies supporting the capacitance method, hydroponic laboratory results of Dietrich et al. (2012) and other studies have begun to uncover potential inconsistencies with Dalton’s assumptions. In their work, Dietrich et al. (2012) explored the effect of trimming submerged roots on the BIA response and found negligible variation of the root capacitance. Cao et al. (2010) reached similar conclusions regarding the measured electrical root resistance (overall electrical resistance for the electric circuit obtained with injection into the stem and return electrode in the hydroponic solution, Fig. 1a). Urban et al. (2011) discussed the BIA hypotheses and found that the current left the roots in their proximal portion in several of their experiments. Conclusions from the latter study are consistent with the assumption that distal roots have a negligible contribution on root capacitance and resistance.
Because of the complexity of the hydraulic and electrical pathways, their link has long been the object of scientific research and debate. For recent reviews see Aroca (2012) and Mancuso (2012); for previous detailed discussions on pathways in plant cells and tissues see Fensom (1965), Knipfer and Fricke (2010), and Findlay and Hope (1976); see Johnson (2013) and Maherali et al. (2009) in regard to xylem pathways. See Jackson et al. (2000) and Hacke and Sperry (2001) for water pathways in roots. Thus, above discrepancies in the link between electrical and hydraulic root properties can be, at least to some degree, attributed to differences among plant species investigated and growing conditions.
Among herbaceous plants, maize has been commonly used to investigate root electrical properties (Frensch and Steudle 1989). For instance, Ginsburg (1972) investigated the longitudinal and radial current conductivities (σcl and σcr) of excited root segments and concluded that the maize roots behave as leaking conductors. Similarly, Anderson and Higinbotham (1976) found that σcr of maize cortical sleeves was comparable to the stele σcl. Recently, Rao et al. (2018) found that maize root conductivity decreases as the root cross-sectional area increases, and that primary roots were more conductive than brace roots. By contrast, BIA studies on woody plants have supported the hypothesis of a radial isolation effect of bark and/or suberized tissues (Čermák et al. 2006; Aubrecht et al. 2006).
Plant growing conditions have been shown to affect both water uptake and solute absorption due to induced differences in root maturation and suberization (e.g., Schreiber 2010). Redjala et al. (2011) observed that the cadmium uptake of maize roots grown in hydroponic conditions was higher than in those grown aeroponically. Tavakkoli et al. (2010) demonstrated that the salt tolerance of barley grown in hydroponic conditions differed from that of soil-grown barley. Zimmermann and Steudle (1998) documented how the development of Casparian bands significantly reduced the water flow in maize roots grown in mist conditions compared to those grown hydroponically. During their investigation on the effect of hypoxia on maize, Enstone and Peterson (2005) reported differences in oxygen flow between plants grown hydroponically and plants grown in vermiculite.
The results reported above and in other investigations (Aroca 2012, and references therein) are conducive to the hypothesis that root current pathways are affected by the growing conditions, as suggested in Urban et al. (2011). For example, the observations by Zimmermann and Steudle (1998) and Enstone and Peterson (2005) may explain the negligible contributions to the BIA signals from distal roots under hydroponic conditions (Cao et al. 2010; Dietrich et al. 2012). At the same time, the more extensive suberization in natural soil and weather conditions could explain the good agreement between the rooting depth reported by Mary et al. (2018) based on the iCSD and the available literature data for grapevines in the field.
To minimize these ambiguities and to develop a more robust approach for non-invasive in-situ root imaging, we aim to develop iCSD inversion code that does not rely on prior assumptions on root architecture and function and use rhizotron experiments to validate the iCSD approach.
Materials and methods
The phrase “inversion of Current Source Density” (iCSD) was introduced by Łęski et al. (2011) to describe the 2D imaging of current sources associated with the brain neural activation. Similar inversion methodologies have been developed for the interpretation of the self-potential data, where the distribution of naturally occurring currents is investigated (Minsley et al. 2007, and references therein). With regard to active methodologies, Binley et al. (1997) developed an analogous approach for detecting pollutant leakage from environmental confinement barriers. Although there are physical and numerical intrinsic differences between application of the iCSD to detect brain neuronal activity and current pathways in roots, we decided to adopt the term iCSD as the general physical imaging of current source density remains valid. With iCSD, we indicate the coupling of ERT and MALM through the proposed numerical inversion procedure for the imaging of the current source density, and its correlation with root architecture.
We introduce the necessary aspects regarding the ERT and MALM methods in this section. However, we direct the interested readers to more in-depth discussion about the ERT method (Binley and Kemna 2005), and to Schlumberger (1920) and Parasnis (1967) with regard to the MALM method.
In the following discussion we use ρmed to represent the 2D or 3D distribution of the electrical resistivity in the growing medium (i.e., hydroponic solution or soil, and with possible influences from RWU and ligneous root mass). CSD represents the 2D, or 3D, distribution of the Current Source Density within the same medium. In the case of roots, the CSD is controlled by the current conduction behavior of the roots, specifically by the leakage pattern of the root system (e.g., proximal or distal current leakage, Fig. 1).
Both ERT and MALM are active methods. In these methods the current is forced through the medium by applying a potential difference between two current electrodes. In ERT, both current electrodes are positioned in the investigated medium, while for MALM the positive current pole is installed in the plant stem, similar to BIA (Fig. 1). The potential field resulting from the current injection depends on CSD, resistivity of the medium (ρmed), and boundary conditions. The boundary conditions are known a priori and their impact on the potential field can be properly modeled. In ERT, the current sources correspond to the electrodes used to inject current, allowing us to invert for ρmed. Then, the iCSD accounts for the obtained ρmed and explicitly inverts the MALM data to obtain current source distribution.
Laboratory setup and data acquisition
The rhizotrons used in this study were designed to enable the concurrent direct visualization of the roots and electrical measurements. Rhizotron dimensions were 52 cm (x) × 53 cm (y) × 2 cm (z), see Fig. 2. Figure 2a shows the rhizotron setup with 64 silver/silver chloride (Ag/AgCl) electrodes located on the back viewing surface. The viewing surfaces were covered with opaque material to stop the light from affecting the development of the roots. The back viewing surface was removable, allowing homogeneous soil packing for the plant experiments and convenient access to the electrodes. Besides the top opening, the rhizotrons were waterproof to enable hydroponic experiments and controlled evapotranspiration conditions during the soil experiments and plant growth. All the experiments were performed in a growth chamber equipped with automatic growth lights (LumiGrow Pro650e) and controlled temperature and humidity. The temperature varied with a day/night temperature regime of 25/20 °C. The humidity ranged from 45 to 60%.
For both ERT and MALM methods, the electrical potential field is characterized by a set of potential differences (∆V) measured between pairs of electrodes. It is important to properly arrange the electrodes on the rhizotron viewing surface and design a suitable acquisition sequence to obtain a good sensitivity coverage (hereinafter coverage) of the investigated system (Slater et al. 2002). This is particularly true for the iCSD, as both ERT and MALM acquisitions affect its result.
The 64 electrodes were arranged in a 8 by 8 grid on the back viewing surface of the rhizotron, leaving the front surface clear for the observation (Fig. 2). For the ERT, the designed arrangement of the electrodes offers a good compromise between a high coverage on the central part of the rhizotron, which encompasses the root zone, and a sufficient coverage on the rhizotron sides to avoid an excessive ERT inversion smoothness.
For the MALM, the arrangement of the electrodes is highly sensitive to the position of the investigated current sources. Because of their central positions, the electrodes are closer to the expected sources of current (i.e., the roots) and thus in the region of maximum potential gradient. Hence, this electrode configuration maximizes the changes in both magnitude and sign of the measured ∆V associated with a change in the CSD distribution.
The electrode diameter was 1.5 mm. The penetration of the electrodes into the rhizotron was 4 mm ± 1 mm. To evaluate the possible distorting effects of the densely populated electrodes on the potential field distribution, a test was performed with low conductivity water (20 μS cm−1). The test showed no resistivity anomalies, which may be caused by the presence of the electrodes (data not shown). Therefore, while rhizotron setups with electrodes only on the sides were successfully adopted (Weigand and Kemna 2017), we found that the current setup represents a better solution for iCSD experiments (Fig. 2).
Data were acquired with a MTP DAS-1 resistivity meter with 8 potential channels. For the ERT acquisition over the 2D grid of electrodes, we chose a dipole-dipole skip 2 configuration. For each skip 2-couple of injection electrodes (e.g., electrodes 1 and 4) the remaining skip-2 couples of electrodes were used as potential dipoles (e.g., electrodes 5 and 8, 6 and 9, etc.). The associated complete set of reciprocals was also acquired, the resulting acquisition sequence contained 3904 data points (Binley and Kemna 2005; Parasnis 1988; Mary et al. 2018).
Following the ERT data acquisition, the MALM data acquisition required little setup adjustments and time. As the two current electrodes are fixed, the use of a multichannel resistivity meter significantly reduced the acquisition time and, consequently, supported the acquisition of more robust data sets. Electrode 1 was used to inject the current into the plant stem, while electrode 64 was used as a return electrode in the growing medium (Fig. 1d). The remaining 62 electrodes were used to map the resulting potential field. A sequence with 204 ∆Vs was used. Considering the grid in Fig. 2a, the sequence included the vertical, horizontal, and diagonal ∆Vs between adjacent electrodes. While 61 ∆Vs would provide all the independent differences, the 204 ∆V sequence was preferred because of its redundancy and consequent lower sensitivity to acquisition errors. The acquisition time remained relatively short (2–3 min) as the multichannel instrument was optimized with fixed current electrodes that allowed 8 ∆Vs to be measured at once.
Data processing and ERT inversion
ERT and MALM data were filtered considering: 1) reciprocal error (5% threshold), 2) stacking error (3 stacks, 5% error threshold), 3) minimum measured ∆V (minimum 0.5 mV threshold), 4) apparent resistivity (the range changed among different data sets), and 5) maximum electrode contact resistance (30 kohm). The filtering was implemented to enhance the control on the ERT inversion and obtain a reliable ρmed for the successive iCSD inversion.
After the processing, the data were inverted with the BERT inversion software to obtain ρmed (Günther and Rücker 2013; Rücker et al. 2006; Günther et al. 2006). Data error was set to 5% in line with the stacking and reciprocal thresholds used for the data filtering. The regularization was adjusted using the lambda optimization algorithm provided by the BERT software. Generally speaking, a rhizotron is treated as a 2D geometry. However, this bounded and thin geometry leads to some complications into the ERT inversion. Specifically, no-current-flow boundary conditions were set for all the rhizotron surface and the inversion had to be adapted for the resulting pure Neumann problem (Bochev and Lehoucq 2005). For a higher quality forward calculation, the rhizotron volume was discretized in 3D by extruding a 2D mesh with 5 layers. The discretization allowed the refinement of the mesh near the electrodes while maintaining high mesh quality. At the same time, in order to limit the inversion time and force the inversion to be two-dimensional (x, y), the elements in z direction (resulting from the extruded layers) were grouped together and inverted as a unique variable. This way, a 3D forward calculation was implemented within a 2D inversion (Ronczka 2016).
The iCSD inversion that we developed was based on the physical principles of a bounded system in which linearity and charge conservation were applied to decompose the investigated CSD distribution into the sum of point current sources. This provided a discrete representation of the root system portions where the current leaks from the roots into the surrounding medium.
Because of the linearity of the problem, the collective potential field from multiple current sources is the linear combination of their individual potential fields. As such, the measured ∆V can be viewed as and decomposed into the sum of multiple ∆Vs from a set of possible current sources. These possible current sources are named ViRTual electrodes (VRTe). As purely numerical (virtual) electrodes, they are simulated by mesh nodes representing possible current sources, but with no direct correlation with the real (physical) electrodes used during data acquisition. Basically, the VRTe were distributed to represent a grid over which the true CSD distribution is discretized. In order to account for any possible CSD, a 2D grid of 306 VRTe was arranged to cover the entire rhizotron (Fig. 2b).
The charge conservation law implies that the sum of the current fractions associated with the VRTe (hereinafter VRTe weights) has to be equal to the overall injected current, which is provided by the resistivity meter. If we normalize the injected current to be equal to 1, the sum of the VRTe weights has to be 1 as well. Briefly, for Ohm’s law, normalizing the current to 1 is equivalent to calculating the resistance, R, from ∆V. Then, the use of R simplifies the presentation of the numerical problem.
Once the VRTe nodes are added to the ERT-based ρmed structure, the potential field associated with each of the VRTes is simulated with BERT. From these simulated potential fields, the same sequence of 204 R is extracted, each corresponding to a single VRTe. Each extracted sequence contains the resistances that would be measured in the laboratory if all the current sources were concentrated at the VRTe point (i.e., VRTe Green’s function).
The VRTe weights are the unknowns that the iCSD strives to estimate. Once the VRTe weights are estimated and associated with the respective VRTe coordinates, they provide a discrete visualization of the investigated CSD. The problem of estimating the VRTe weights that decompose the measured R sequence into a sum of the simulated VRTe R sequences is analogous to a linear vector decomposition (Strang 1976), and is expressed by:
Where A is a matrix, its columns are the simulated VRTe R sequences; x is a vector containing the unknown VRTe weights; b is a vector containing the measured sequence of 204 R. Each row in A corresponds to the relative R in the acquisition sequence, e.g., A1,1 is the first resistance extracted from the potential field simulated with injection at the first VRTe.
The charge conservation is implemented by appending a row of 1’s to A and a corresponding 1 to the vector b. This forces the sum of the VRTe weights to be equal to 1. A weight of 1000 was used to guarantee the charge conservation; with a lower weight observations and regularization may dominate the charge conservation.
Since the problem is undetermined, a first order spatial regularization is added (Menke 1989). Rows are added to express the differences between adjacent (vertically and horizontally) VRTe, e.g., the row [1 − 1 …] is the difference between the first two VRTe weights. The differences are added for the entire VRTe grid and set to 0 by adding corresponding 0’s to b.
Lastly, the trade-off between data misfit and solution regularization is controlled by a diagonal weight matrix W. The numerical routine includes a “pareto” functionality wherein regularization and model-to-measurement fit are traded off while changing the regularization weight, i.e., running the inversion with different regularization weights. The obtained set of solutions can be used to construct the “pareto front” (L-curve), which is a widely accepted way to estimate the optimum regularization weight (Hansen and Dianne 1993). Eq. 2 shows the resulting system WAx = bW.
Where S indicates the n VRTe sources, R the m resistances, and w the weights used to control the solution regularization.
Lastly, the solution is further constrained by forcing the linear solver to seek only positive VRTe weights (i.e., inequality constraint), as the negative source of current is known to correspond uniquely to the return electrode.
The linear problem formulation is conducive to the inversion optimization during the calculation of the pareto front. The calculation time of the Pareto front can be further reduced by code optimization as the calculations that do not depend on the regulation weights can separated from the inversion routine and performed only once during the initialization of the linear problem. The initialization phase includes the processing of the MALM experimental data, forward calculation of the VRTe responses for the given ρmed, inclusion of the continuity constraint, and construction of the matrices.
Continuity constraint, bounded-value constraint, and first-order spatial regularization stabilize the inversion while limiting the impact of the spatial regularization strategy. The impact of the spatial regularization was evaluated by monitoring the relative components of the misfit and the resulting distribution of the current source. In both synthetic and laboratory tests, as well as in plant experiments the iCSD results are often limited to few current sources (Figs. 3, 4, 7, and 9).
Synthetic and experimental iCSD testing
Synthetic numerical and laboratory experimental tests were performed in order to evaluate the capabilities of the setup and inversion routine to couple the ERT and MALM approaches for the iCSD. In the numerical tests both the true source response and VRTe responses were calculated with BERT.
Figure 3 shows an explanatory numerical test with inversion of a point source, and the associated Pareto front that was used to select the optimum regularization strength. As this first experiment was performed to specifically test the inversion routine, a homogeneous ρmed was used in order to avoid influence from the baseline resistivity distribution complexity.
For the second experiment, the laboratory tests were conducted. Because of the ρmed heterogeneity of any experimental system, these laboratory tests need to include the ERT inversion, and the use of the obtained ρmed as input in the iCSD. The true current sources were obtained using insulated metallic wires inserted into the rhizotron (Fig. 4). The insulating plastic cover was removed at the tips (1 cm, red dots in Fig. 4a) of the metallic wires to obtain the desired current sources. Six experimental tests were performed using different numbers and positions of these current sources. The rhizotron was filled with tap water and left to equilibrate to achieve steady state conditions of water temperature and salinity, thus minimizing ρmed heterogeneity and changes during the experiment. Changes in ρmed during the ERT and MALM acquisition periods would make the ERT-based ρmed less accurate and compromise the iCSD. To make sure ρmed was stable, a second ERT was performed after the MALM acquisition and compared with the initial measurement. The conductivity of the solution was also measured in several locations of the rhizotron with a conductivity meter to validate the ρmed obtained from the ERT inversion. This setup allowed the acquisition of good quality data sets since less than 5% of the data were discharged during the data processing. Because of the controlled laboratory conditions, the ρmed obtained with the ERT was stable and consistent with the direct conductivity measurements. The quality of the ERT inversion was also confirmed by comparing the model responses with the acquired data (i.e. data misfit). Similarly, the acquired iCSD data were plotted against the resistances calculated with the CSD distribution obtained from the iCSD.
The tests also allowed a more informed definition of the VRTe grid. For our setup, a spacing of 3 cm provided a good compromise between resolution, stability, and duration of the iCSD routine. The 3-cm spacing also agrees with the ERT resolution, which would not support a higher iCSD resolution.
Successive numerical tests were based on the 8-source laboratory tests shown in Fig. 4. These tests aimed to 1) link laboratory and numerical tests to evaluate the influence of the numerical iCSD routine and laboratory setup on the overall iCSD stability and resolution; 2) account for a more complex CSD, given by the 8 wire-tip sources that were used to simulate distal current pathways; and 3) account for possible ρmed heterogeneity. To address goals 1 and 2, the position of the 8 sources was replicated in the numerical tests and a test with homogeneous ρmed was included to simulate the water resistivity of the laboratory tests. To address goal 3, heterogeneous ρmed were tested.
In order to account for the heterogeneous ρmed the following modeling steps were carried out. First, a true ρmed was assigned to the mesh cells of the rhizotron ERT model. We included homogeneous, linear, and quadratic resistivity profiles in the y direction, see Fig. 5. Second, the ERT acquisition was simulated (i.e., forward calculation) with the ERT laboratory sequence and 3% of Gaussian error, in line with reciprocal and stacking errors observed in the laboratory data sets. Third, the forwarded ERT data sets were inverted following the exact laboratory procedure. A refined and different mesh was used for forward and inverse problems to, respectively, increase the simulation accuracy and avoid the inverse crime (Wirgin 2004). The ERT forward calculation was then repeated over the inverted ρmed. The obtained inverted responses were compared with the responses of the true models.
As for ERT, we compared true and inverted MALM responses. First, the true response was simulated with the 8 current sources overt the true (not inverted) ρmed. Second, a MALM response was calculated over the inverted ρmed and inverted to obtained the inverted CSD. Third, the obtained inverted CSD was used to forward calculate the inverted MALM response over the inverted ρmed. True and inverted MALM responses were then compared.
We performed hydroponic and soil experiments using maize and cotton plants. In all the plant experiments, the injection electrode was positioned in the plant stem at a height of 1 cm from the surface of the growth media.
For the hydroponic experiments, the plants were first grown in columns with aerated nutrient solution (Hoagland and Arnon 1950). They were then moved to the rhizotron for the experiments. As in the metallic roots test, the rhizotron was filled 1 day before the experiment to reach stable and homogeneous temperature and salinity conditions. The plant was positioned at the center of the rhizotron with soft rubber supports. The plants were submerged at the same level as in the growing column to avoid discrepancies caused by the plant tissue adaptation to the submerged and aerated conditions, as discussed above with regard to the growing conditions. Consequently, the root crown was approximately 3 cm below the water surface.
For the soil experiments, seedlings were grown directly in the rhizotron to avoid damaging the roots and altering the root-soil interface. The soil was prepared by mixing equal volumes of sandy and clay natural soils acquired from an agricultural study site run by U.C. Davis, CA (Russell Ranch). The plants were irrigated with double strength Hoagland solution (Hoagland and Arnon 1950).
Two soil experiments were performed. In the first experiment, four cotton plants were grown for four months. For these experiments, the plants were positioned with the root crown approximately 8 cm deep (y = 0.44 m). In the second experiment, a pregerminated maize seed was planted 3 cm deep and then grown for four months (Fig. 10).
Figure 3 shows the result of a synthetic numerical test performed to evaluate the iCSD resolution, inversion stability, and influence of imposed constraints. The obtained CSD matches the true position of the simulated current source. The sum of the current sources equals 1 as expected and required by the continuity constraint. The resolution of the CSD is in line with the electrode interspace (5 cm). The first-order regularization (smoothness constraint) does not hinder the reconstruction of simulated point source.
Figure 4 shows the results of a laboratory experiment where the iCSD method was tested with a known distribution of current sources obtained with metallic wires. The use of metallic wires offered a comprehensive solution to test the overall correct functioning of the laboratory setup and inversion routine. The iCSD correctly characterized both position and intensity of the test sources with no need for prior information to constrain the solution. The asymmetrical distribution CSD agrees with the principle of path of least resistance, i.e., the closer to the return electrode, the shorter the water path, the higher the current source density. The obtained distribution of current source agrees with true CSD and resolution expected on the basis of previous numerical tests. The iCSD resolution was sufficient for the imaging of a root-like structure, e.g., differentiate between distal, proximal, or equally distributed current pathways in the roots (Fig. 4c). In this case, a distal CSD was investigated (tips of the metallic wires) and the iCSD correctly found no proximal current source (near the immersion point of the root-like metallic structure).
Figures 5, 6, and 7 show the results of the synthetic tests based on the 8-source laboratory tests. Figure 5 compares the true (a) and inverted (b) ρmed to highlight the overall influence of rhizotron meshing, acquisition sequence, processing, and inversion. Figure 6a offers a more quantitative comparison between true and inverted ERT responses. Similarly, Fig. 6b presents the correlation between true iCSD response (true ρmed and true CSD) and the inverted iCSD response (inverted ρmed and inverted CSD). ERT and iCSD inverted responses correlate with the associated true responses (all correlation coefficients >0.95). Figure 7 shows the inverted CSD distribution and confirms the iCSD capability to characterize both intensity and position of the current sources with a resolution of 3 cm.
Plant Experimental Results.
The plant experiments investigated the root current pathways combining the iCSD with the direct observation of the roots. Hydroponic and soil experiments were performed with maize and cotton plants. Figure 8a shows the root architecture for one of the two plant hydroponic experiments with maize plants. Although the roots were visually observed to extend deeper in the rhizotron, both the inverted CSD distributions show that the current leakage in this hydroponic system primarily occurred in the proximal root part at the top of the rhizotron. In particular, the highest current density was predominantly concentrated near the root crown with the remaining current leakage already occurring along the submerged stem section. The ρmed obtained from the ERT inversion confirmed the expected homogeneous temperature and salinity conditions.
In the soil experiments with cotton plants, the iCSD method successfully located the root position of the four plants along the soil surface and produced consistent signals corresponding to the root crowns (Fig. 9). The results also show a localized current leakage near the root crowns with no appreciable current leakage along the four stem sections in the soil or in the distal portions of the root systems. By contrast to the cotton results, the CSD distribution obtained from the maize experiment conducted within the soil presents current leakage along the stem section (Fig. 10).
The ERT-based ρmed obtained from the cotton soil experiments presents a strong heterogeneity with a highly resistive layer at the top of the rhizotron, representing a dry soil layer (Fig. 9b). The evolution of this dry layer is due to water loss through evapotranspiration. The ERT results highlight the need to account for the heterogeneity of ρmed in order to correctly calculate the responses of the VRTes during the iCSD. The ERT results also show how the ERT characterization can support the interpretation of the iCSD results by providing information on the soil characteristics and thus on possibly associated physiological responses, such as drought and suberization.
iCSD routine results
Both numerical and laboratory iCSD tests successfully image the CSD without requiring prior assumptions on the actual distribution of the roots and CSD. These assumptions were present in previous works (e.g., Mary et al. 2018) but were here replaced by application-specific constraints (smoothness, charge conservation, and positivity). In this sense, not only the explicit linear formulation allowed a direct implementation and evaluation of the these constraints, but also enabled full characterization of the resulting liner problem (e.g., condition number, uncertainty analysis; see Strang (1976) and John (2015)).
Relative to the field setup of Mary et al. (2018), the laboratory setup offered the advantages of more flexible positioning of the electrodes and consequently better ERT and MALM data coverage. The other significant advantages over previous studies were the reduced number of VRTe in a 2D distribution and the new iCSD routine resulting from the 2D distribution of the VRTe and trans-dimensional ERT inversion.
The inversion times was significantly reduced by the proposed iCSD, particularly thanks to its linear formulation, use of specific constraints and code optimization. Solving the linear system described above (Eq. 2) took less than 3 s on a standard laptop, compared to a few minutes using the generic optimization process used in Mary et al. (2018). The reduced inversion time also offers the advantage of a faster calculation of the Pareto front, which allowed a more informed inversion regularization.
Finally, the coupling between ERT and iCSD through the python geophysical library eased the optimization of the entire routine (Rücker et al. 2017). Coupling ERT and iCSD is a relevant aspect of our procedure because the ERT data processing/analysis routine has a strong influence on the successive iCSD inversion, which may require the entire procedure to be repeated to test different ERT inversion parameters (e.g., Fig. 9).
The iCSD results showed that the current leakage occurred in the very proximal regions of the root systems in both soil and hydroponic conditions. The proximal leakage was observed despite the return electrode being placed at the bottom of the rhizotron to allow deep current pathways. Nonetheless, the expected influence of the return electrode position was observed in the laboratory test with metallic roots and motivates the use of this electrode configuration in future laboratory experiments.
Our results are consistent with the early studies on maize root electrical properties (Ginsburg 1972), and corroborate the recent works that questioned the assumptions of the BIA methods (Dietrich et al. 2012; Urban et al. 2011). The high resistivity of the top layer of soil (Fig. 9) is expected to induce root suberization (see Introduction): our results would support the physiological hypothesis of water and nutrient absorption through older and possibly suberized roots (Aroca 2012; Kramer 1946).
It is worth noticing that the absence of current leakage along the section of the cotton stems in the top dry soil supports the assumption that the electrical structure of roots controls their current conduction behavior. Suberized epidermal cells can affect the movement of ions and, consequently, the current conduction in roots (Cseresnyés et al. 2013; Čermák et al. 2006). Therefore, it is feasible for current to be conducted along deeper portions of the more woody roots with minor leakage. The BIA experimental results that have observed positive correlations between electrical signals and root area are likely a result of physiological correlations between the root regions that contribute to the current flow and hair roots, which contributes most to functional root surface area (Fig. 1c). While correlations between BIA electric signals and investigated root traits appear to be indirect, the correlations observed across experimental platforms and species continue to validate its value for in-situ root phenotyping (Dietrich et al. 2012).
In their study on field grapevines, Mary et al. (2018, 2019, 2020) concluded that the CSD could be used to infer the root depth distribution. Because of the significant suberization of major roots in grapevines and orange trees, the electric current could penetrate deep into the root system before significant leakage occured. The deeper current penetration allowed the iCSD method to access and phenotype the root system. On the contrary, limited current results in lower sensitivity of the iCSD to distal and younger parts of the root system that are likely dominated by less suberized, finer roots. We attribute differences in current penetration among root systems of maize, cotton, grapevine, and orange tree to the differences in physiological traits such as the extent of suberization and lignification. If on one hand the sensitivity to the root physiological traits is a promising opportunity, on the other hand it has to be accounted for when phenotyping more herbaceous roots.
In this study we present a novel numerical inversion routine for inversion of current source density in a bounded and non-homogeneous medium. The new inversion procedure offers an explicit matrix formulation that takes advantage of the problem linearity and constraints. The improvements provided by our numerical inversion technique enable a faster and more controlled imaging of the current source density. The numerical inversion routine was also coupled with an existing ERT inversion code to ease the overall inversion procedure. The iCSD inversion code was based on top of an open source geophysical Python library (Rücker et al. 2017).
After testing the method using synthetic numerical and laboratory experiments, we designed a specific rhizotron setup for laboratory plant experiments with maize and cotton. We found that with the obtained electrical coverage, the iCSD correctly characterized the different CSD distributions used in the tests, including the imaging of a root-like structure (Figs. 4, 6, and 7). By contrast to the results reported by Mary et al. (2018), the experimental setup and the new numerical inversion procedure did not require prior assumptions on the root distribution to stabilize and regularize the inversion. By eliminating the need for imputing prior information, our inversion protocol excludes the possibility of obtaining biased solutions.
In all seven plant experiments, the current left the root pathway in its proximal portion, radially leaking into the surrounding growth medium. These results corroborate recent studies that questioned the BIA assumptions (Urban et al. 2011; Dietrich et al. 2012). While these studies provided a thoughtful discussion on the topic, they were based on time-consuming, invasive and less direct observations that restricted the ability to elucidate the complexity of root types and adaptation (e.g., excavation and trimming). This study describes the first direct and concurrent characterization of the root-soil current pathway and root architecture. Intrinsic differences in the root electrical properties of maize, cotton, grapevines, and orange trees emerge from the combined interpretation of our results with those presented by Mary et al. (2018, 2019), and Mary et al. 2020).
The laboratory rhizotron setup offered significant advantages for the development of the iCSD approach. Such advantages include the attainment of optimal electric coverage, direct root observation, and prior information on the growing medium. However, the development of the iCSD approach is well-timed and in line with the development of the geoelectrical technology for field-scale agricultural applications. The technological development driven by the use of ERT and SIP can readily be transferred to the iCSD approach. For example, the increased use of borehole electrodes and resistivity meter capabilities allow high electric coverage at the field-scale. The implementation of long-term monitoring has also become more common and provides precious information to characterize the dynamics of soil and vegetation. In this sense, the iCSD is a non-invasive solution that could be used to monitor the changes in root current pathways in response to water stress and other environmental factors. In conclusion, our inversion approach fills a major gap toward the full implementation of methods that allow non-destructive imaging of roots in their natural soil environment.
Current Source Density
inversion of Current Source Density
- σcr :
radial electric current conductivity of roots
- σcl :
longitudinal electric current conductivity of roots
- ρmed :
electric resistivity distribution of the growing medium.
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Luca Peruzzo and Myriam Schmutz gratefully acknowledge the financial support from IDEX (Initiative D’EXellence, France). Yuxin Wu acknowledges the support of ARPA-E ROOTS (Advanced Research Projects Agency - Energy, Rhizosphere Observations Optimizing Terrestrial Sequestration, Lawrence Berkeley National Laboratory). Susan Hubbard acknowledges the support of the Watershed Function Scientific Focus Area, which is funded to Berkeley lab by the U.S. Department of Energy, Office of Science, Office of Biological and Environmental Research under Award Number DE-AC02-05CH11231. The authors thank the members of the editorial board, the anonymous reviewers, and Maximilian Weigand for their contributions. ERT and iCSD codes, with data from this study, are maintained at https://github.com/Peruz/ERTpm and https://github.com/Peruz/icsd.
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Peruzzo, L., Chou, C., Wu, Y. et al. Imaging of plant current pathways for non-invasive root Phenotyping using a newly developed electrical current source density approach. Plant Soil 450, 567–584 (2020). https://doi.org/10.1007/s11104-020-04529-w
- Root current pathways
- Root imaging
- Current source density
- Electrical resistivity tomography
- Mise a la masse