# Impact of growth and uptake patterns of arbuscular mycorrhizal fungi on plant phosphorus uptake—a modelling study

## Abstract

In this paper we present a mathematical model for estimating external mycelium growth of arbuscular mycorrhizal fungi and its effect on root uptake of phosphate (P). The model describes P transport in soil and P uptake by both root and fungi on the single root scale. We investigate differences in soil P depletion and overall P influx into a mycorrhizal root by assuming that different spatial regions of mycelia are active in P uptake. When all external hyphae contribute to P uptake, overall uptake is dominated by the fungus and the most effective growth pattern appears to be the one using a high level of anastomosis. The same is true when only the proportion of external hyphae assumed to be active contributes to uptake. When uptake is restricted to the tips, hyphal contribution to overall P uptake is less dominant; the most effective growth pattern appears to be the one characterised by nonlinear branching where branching stops at a given maximal hyphal tip density. Comparison to measured P depletion in the literature suggests that the scenario where active hyphae are contributing to P uptake is likely to fit the data best. These quantitative predictions promote our understanding of the mycorrhizal symbiosis and its role in plant P nutrition.

## Keywords

Arbuscular mycorrhiza Fungal growth Mathematical model Plant phosphorus uptake## Introduction

Phosphorus is one of the essential mineral nutrients for plants. The preferred form of phosphorus taken up by plants is ortho-phosphate^{1} (Vance 2003). Due to the fact that phosphate (P) is generally not very mobile in soils, narrow depletion zones in the order of millimetres form around P-absorbing roots (Hinsinger et al. 2005). Low phosphate concentrations in soil can be limiting for plant growth. Therefore, plants have developed mechanisms, such as symbiotic relations with soil fungi, to increase their access to soil phosphate. Probably the most important symbiotic mechanism is the formation of mycorrhizas, mutualistic symbiotic associations between plant roots and specific soil fungi. Arbuscular mycorrhizas are the most widespread type of mycorrhiza formed by the majority of crop plant species and more than 70% of all terrestrial plants (Brundrett 2002). In the current paper, only arbuscular mycorrhizal associations are examined. In addition to the direct uptake pathway via roots, arbuscular mycorrhizal (AM) fungi provide plants with an additional pathway for P uptake. They are able to deliver P which would otherwise not be directly accessible for the plant (Zhu et al. 2001). This pathway includes P uptake from soil by the external fungal mycelium, translocation towards the root surface, and transfer into the root cortical cells. In rhizosphere models, P uptake from soil by both roots and fungi is usually described by Michaelis–Menten kinetics (Barber 1995; Schweiger and Jakobsen 1999). However, uptake can be more complex, following two independent Michaelis–Menten type systems, *i.e.*, a high and a low-affinity transport mechanism. For some plant species, the presence of up to seven transport kinetics has been suggested and the molecular and biochemical characterisation of the corresponding P transport systems is currently extensively studied (Bucher 2007; Raghothama and Karthikeyan 2005).

*i.e. Scutellospora calospora*isolate WUM 12(2),

*Glomus sp*. isolate WUM 10(1) and

*Acaulospora laevis*isolate WUM 11(4) which were examined in a study of Jakobsen et al. (1992a). The hyphal length and tip densities resulting from calibrating the model of Schnepf et al. (2007) to the measured hyphal length densities are shown in Figs. 4 and 5, respectively. The fungal growth processes apical branching (tip splitting), tip–hyphae anastomosis and tip–tip anastomosis which account for the different fungal growth patters used in the model are depicted in Fig. 1.

*Scutellospora calospora* WUM 12(2) appeared to receive a lot of support from the root-soil boundary for the creation of new hyphal tips, and it produced the largest biomass of all fungal species considered. By support we mean the supply of carbon or energy from inside the root to the fungus. The growth pattern of this fungus was called linear branching pattern as the rate of tip splitting was linearly proportional to the hyphal tip density. *Glomus sp.* WUM 10(1) was found to be described best by nonlinear branching where branching ceases at a maximal hyphal tip density, possibly due to competition for resources. The main pattern of *Acaulospora laevis* WUM 11(4) was considered to be tip–hyphae anastomosis, characterised by the formation of an interconnected network. The most distinct feature of this fungal species was the presence of a peak of hyphal length density at the front of the colony (Jakobsen et al. 1992a; Schnepf et al. 2007). All fungal species grew up to ten centimetres away from the root surface within 47 days. Thus, the external fungal hyphae provided the plants with the possibility to exploit a large soil volume they could not access on their own. It is the goal of this paper to investigate the impact of the different AM fungal growth patterns on plant P nutrition. In particular, we will show the differences in soil exploitation and in overall P influx into a mycorrhizal root which is colonised by AM fungi with different growth patterns.

Increased P uptake by arbuscular mycorrhizal plants is generally attributed to the increased surface area available for uptake. However, it is less clear exactly how large this increased surface area for uptake is. It is often assumed that AM fungal hyphae take up nutrients along their entire length (Schweiger and Jakobsen 1999). However, experimental results have led some authors (Boddington and Dodd 1999; Ezawa et al. 2003) to distinguish between a metabolically active and inactive part of the mycelium, implying that only the active part is contributing to P uptake. Also morphological studies of the external mycelium of AM fungi have led some authors to suggest that only a part of the mycelium is acquiring P (Bago 2000). The results from another study again (Jolicoeur et al. 1998) suggest that hyphal P uptake only occurs in a small region behind the hyphal tips. With our model, we test these hypotheses on mycorrhizal uptake patters for all three fungal growth patterns and quantify how they are expected to influence the plant P uptake. Furthermore, we assess differences in spatial P acquisition and how they are related to gross structural features such as hyphal length densities.

## Model development

### Motivating experiment and choice of model geometry

This experimental setup motivates the choice of geometry for our model. When the roots in the root compartment are very dense, the dynamics of root growth within this compartment can be neglected and the membrane can be regarded as the root-soil boundary. One-dimensional Cartesian coordinates are appropriate for this system since changes in P concentration and hyphal length densities are only measured with respect to their distance from the planar root-soil boundary.

We use the model that was first described in Schnepf et al. (2007) to describe AM fungal growth. The creation of a P sink term based on the fungal growth model and the uptake capacity of the external hyphae is described in Schnepf and Roose (2006). This paper combines and extends the work of these two previous publications and examines how different growth and uptake patterns of AM fungi are expected to affect the total P uptake of a mycorrhizal root.

### Model for soil P concentration near a mycorrhizal root

*x*is the distance from the root surface,

*t*is time,

*b*is the soil buffer power,

*θ*is the volumetric water content,

*f*is the impedance factor,

*D*is the diffusion coefficient in free solution,

*q*is the Darcy flux of water towards the root surface,

*F*

_{m}is the maximal influx of solute into root,

*K*

_{m}is the Michaelis–Menten constant of the root,

*c*

_{0}is the initial solute concentration in soil,

*ρ*is the hyphal length density,

*n*is the hyphal tip density, and

*F*

_{myc}is the volumetric sink term that represents solute uptake by the fungal mycelium. The expression for

*F*

_{myc}is based on a model for the growth of the external mycelium as well as on a model for P uptake by individual hyphae. Due to the low mobility of P in soils, depletion zones around single hyphae may in some cases develop similar to the depletion zones created around roots. However, Schnepf and Roose (2006) found that the depletion zone around a single hypha is negligibly small when hyphal uptake is small compared to diffusion in soil. This is the case when \(\frac{{F_{{\text{m,h}}} }}{{K_{{\text{m,h}}} }} \ll \frac{{D\theta f}}{{r_{\text{h}} }}\), assuming that the parameters describing diffusion, hyphal uptake and hyphal radius are constant. This condition holds for given soil and fungal uptake properties as long as the hyphal radius

*r*

_{h}is smaller then \(\frac{{D\theta fK_{{\text{m,h}}} }}{{F_{{\text{m,h}}} }}\). Because of the small radius

*r*

_{h}of a hypha which is in the order of micrometers, this will be true for most fungal species in soil. For example, if we consider the soil and fungal uptake properties used in this study (see Tables 1 and 2 below), the hyphal radius would have to be bigger than 22 μm for this condition not to hold. Therefore, in the current study, we will assume that the hyphal radius is smaller than 22 μm and that the concentration gradients around hyphae are negligibly small. Under the further assumption that hyphae can take up P along their entire length, Schnepf and Roose (2006) showed that in this case the sink term

*F*

_{myc}can be expressed as

*F*

_{m,h}is the maximal influx into hyphae,

*K*

_{m,h}is the Michaelis–Menten constant of hyphae,

*c*is the local concentration of solutes in soil,

*ρ*is the local hyphal length density, and thus

*2πr*

_{h}

*ρ*is the total surface area of extraradical hyphae. Modifications of Eq. 5 will be related to hyphal growth and uptake patterns, and the effect of this on overall P influx into a mycorrhizal root will be investigated.

Parameter values for P transport model

Symbol | Name | Units | Value | Source |
---|---|---|---|---|

| Diffusion coefficient in free solution | cm | 10 | Lide (2000) |

| Volumetric water content | cm | 0.3 | Barber (1995) |

| Impedance factor | cm | 0.308 | |

| Darcy flux | cm s | 10 | Barber (1995) |

| Buffer power | cm | 239 | Barber (1995) |

| Initial concentration of P in solution | μmol cm | 10 | Barber (1995) |

| Maximal influx of P into root | μmol cm | 3.26 × 10 | Tinker and Nye (2000) |

| Michaelis–Menten constant for root P uptake | μmol cm | 5.8 × 10 | Tinker and Nye (2000) |

Parameter values for hyphal uptake

Symbol | Name | Units | Value | Source |
---|---|---|---|---|

| Hyphal radius | cm | 5.0 × 10 | Ezawa et al. (2002) |

| Maximal influx of P into hypha | μmol cm | 3.26 × 10 | Same values as for root |

| Michaelis–Menten constant for hyphal P uptake | μmol cm | 5.8 × 10 | Same values as for root |

### Fungal growth model

*ρ*(

*x*,

*t*) required in Eq. 5. Hyphal tips move through the soil due to elongation of the zone just behind the tips. The hyphal length density

*ρ*is regarded as the trail left behind by the tips, decreased by hyphal death. New tips are created by apical branching and the number of tips is reduced by tip death, tip–tip and tip–hypha anastomosis. Since arbuscular mycorrhizal fungi are obligate symbionts and are always attached to the root, we need to take the effect of the root-soil boundary into account. In this paper we assume that hyphal tips appear at the root-soil boundary and that the number of tips increases linearly with time. This hyphal population growth model has macroscopic outputs (hyphal length and tip densities), but it is based on average properties of the individual hyphae. The equations describing fungal growth are given by

*v*is the tip elongation rate,

*d*is the hyphal death rate,

*b*

_{ n }is the tip branching rate,

*n*

_{max}is the maximal tip density,

*d*

_{ n }is the tip death rate,

*a*

_{1}is the tip–hypha anastomosis rate,

*a*

_{2}is the tip–tip anastomosis rate,

*a*is the proliferation parameter for the hyphal tip density at the root-soil boundary, and

*n*

_{0,b }is the initial tip density at the root-soil boundary.

### Adaptations to the sink term *F* _{myc}

*F*

_{myc}given by Eq. 5. According to the different assumptions with regard to which parts of the mycelium are contributing to P uptake as described in the introduction, we will consider three different uptake scenarios. “Full length uptake” is based on the condition that hyphae are capable of taking up phosphate along their entire length so that

*F*

_{myc}is given by Eq. 5. The “tip uptake scenario” assumes that hyphal P uptake occurs only along a defined length of hypha at and behind the tips. Therefore, we take

*F*

_{myc}to be proportional to the density of the tips, and the sink term

*F*

_{myc}becomes

*z*is the length of the zone behind the tip where uptake occurs. In the “partial length uptake scenario” we consider that only active hyphae are taking up phosphate. The proportion of active hyphae is presented by an additional parameter

*ϕ*so that the sink term

*F*

_{myc}becomes

*ϕ*has a value between 0 and 1. When

*ϕ*= 0 then hyphae are not taking up any P, and when

*ϕ*=

*1*then hyphae are taking up P along their entire length. “Full length uptake scenario” and “tip uptake scenario” represent the most optimistic and the most conservative assumptions with respect to fungal P uptake. They are depicted in Fig. 3. “Partial length uptake scenario” is expected to lie somewhere in between.

### Parameterisation

Parameter values for three fungal growth patterns as found in Schnepf et al. (2007)

Symbol | Name | Units | Linear branching pattern | Nonlinear branching pattern | Anastomosis pattern |
---|---|---|---|---|---|

| Elongation rate | cm s | 2.89 × 10 | 1.50 × 10 | 3.24 × 10 |

| Branching rate | s | 2.31 × 10 | 2.21 × 10 | 1.70 × 10 |

| Tip death rate | s | 6.02 × 10 | 1.74 × 10 | 8.45 × 10 |

| Hyphal death rate | s | 2.08 × 10 | 3.24 × 10 | 9.26 × 10 |

| Inverse of the maximal tip density | cm | 0 | 2.24 × 10 | 1.79 × 10 |

| Tip–tip anastomosis rate | cm | 0 | 0 | 8.10 × 10 |

| Tip-side anastomosis rate | cm | 0 | 0 | 1.74 × 10 |

| Root-soil boundary proliferation rate | cm cm | 2.92 × 10 | 2.59 × 10 | 6.48 × 10 |

| Initial tip density at root-soil boundary | cm | 97.07 | 84.16 | 12.68 |

The sink term *F* _{myc} in the tip uptake scenario requires a value for the length of the zone of uptake near the hyphal tip. Jolicoeur et al. (1998) suggested that the zone of uptake has a width of 50–300 μm behind all tips. In order to take the most conservative approach, we will use a value of 50 μm in the following simulations. It is difficult to specify the parameter value for the proportion of active hyphae required in the partial length uptake scenario where the sink term is described by Eq. 11. To our knowledge, there are no available data that describe the spread of hyphae and at the same time distinguish between active and inactive hyphae. Histochemical staining of enzymes such as alkaline phosphatases has been used as an indicator of fungal viability or metabolic activity (Joner et al. 2000). As a result, part of the extraradical mycelium (given in percentage of the total hyphal length) is viewed as the active part of the mycelium and the rest is viewed as the inactive part of the mycelium. Although different enzymes are associated with different metabolic activities related to internal P transformations, these data indicate that often only part of the mycelium is involved in P uptake and translocation (Boddington and Dodd 1999). When we try to use this information in our model, we have to note that these numbers are not spatially explicit. In a first step, we will therefore estimate, combining information from the work of Boddington and Dodd (1999), Ezawa et al. (2003) and Bago (2000) that 50% of the mycelium at any given time and at any given distance from the root consists of active hyphae, *i.e*., in our model we choose *ϕ* = *0.5*. Thus, from now on, we call the partial uptake scenario “half length uptake scenario”.

### Numerical solution

The model for P uptake by an arbuscular mycorrhizal root associated with one of three arbuscular mycorrhizal fungi with different growth pattern was solved numerically using the finite difference method (Morton and Mayers 1994). Specifically, an implicit finite difference scheme with centred differences in space was used to solve the model for P transport in soil given by Eqs. 1–4. The hyphal growth model given by Eqs. 6–9 was solved numerically using a Lax–Wendroff scheme for hyphal tip density and an explicit Euler scheme for the hyphal length density. All numerical schemes are described in detail in Schnepf and Roose (2006) and Schnepf et al. (2007).

## Results

In this section we present results of the model computations for all combinations of the three different fungal growth patterns and the three different uptake scenarios. Model results include hyphal length and tip densities, P depletion profiles in soil, spatial distribution of P uptake by external hyphae, and the relative contributions of root and hyphae to overall P uptake, as well as an indication for the effectiveness of the mycelium.

### Hyphal length and tip densities

*i.e*., branching ceases at a maximal hyphal tip density. From a biological point of view, this could be the result of competition for resources when the tip density becomes large. Figure 4c shows the hyphal length density when growth follows the anastomosis pattern. It features a characteristic peak in hyphal length density near the front of maximum mycelial spread. In Fig. 5, the tip densities of the three fungal species are presented.

### Phosphate depletion in soil

We assessed the amount of P still left in the soil region where the mycelium is present after 21 days by integrating P concentration profiles shown in Fig. 6 over the domain of the mycelium. In the full length uptake scenario, 13% (anastomosis growth pattern), 32% (linear branching growth pattern) and 57% (non-linear branching growth pattern) of the amount of P assumed to initially having been present in the soil solution are still left on day 21. In the half length uptake scenario, 26% (anastomosis), 40% (linear branching) and 63% (nonlinear branching) of the initial P content are still left. In the tip uptake scenario, depletion by the fungal mycelium is small, 97% of the initial P content are left by all fungal growth patterns. Differences between growth patterns are only in the spatial P acquisition but not in the overall effect.

### Distribution of mycelial P uptake rate

*F*

_{myc}of Eq. 1. Uptake in the tip uptake scenario is lower by a factor 50–100 than uptake in the full and half length uptake scenarios. In the full and half length uptake scenarios, P is mainly taken up near the front of the spreading mycelium for all growth patterns. As it grows away from the root surface, it strongly depletes the soil and only the front of the mycelium grows into fresh, undepleted soil. In the tip uptake scenario, uptake by the fungus following the anastomosis pattern is also mostly occurring at the front of the colony. Contrary to this, uptake is more evenly distributed along the whole extension of the mycelium in the tip uptake scenario when the fungus grows by the linear or nonlinear branching pattern.

### Phosphate influx into the root via the direct uptake pathway

### Relative contribution of fungal mycelium to overall P influx into a mycorrhizal root

### Effectiveness of the fungal mycelium

*E*of mycelial uptake rate versus hyphal length of the mycelium at any given time is given by

*x*

_{c}is the position of the mycelial front. The results for all uptake scenarios are presented in Fig. 10. We use Eq. 12 only for times larger than 2 days, when the mycelium has been sufficiently established. Otherwise, when the total hyphal length is close to zero, we would have a singularity in Eq. 12. For all uptake scenarios and growth patterns, the effectiveness decreases with time because the fungal biomass increases whilst uptake decreases due to depletion. Because of this, some parts of the mycelium may be involved in transport processes inside the mycelium, but are not contributing to uptake. For all growth patterns, as expected, the mycelium is less effective in the half length uptake scenario than in the full length uptake scenario and more effective than in the tip uptake scenario. Table 4 shows the effectiveness for each fungal growth pattern at four different times relative to the most effective growth pattern within each of the different uptake scenarios. This expression reads \(\frac{{E\left( t \right)_i }}{{\max \left( {E\left( t \right)_i } \right)}}\) where

*i*stands for the different fungal growth patterns. In the full and half length uptake scenarios, the fungus with the anastomosis pattern is most effective throughout the simulation period of 21 days (Fig. 10a, c; Table 4); second with respect to effectiveness is the fungus with the nonlinear branching pattern, followed by the one with the linear branching pattern. After 21 days, anastomosis pattern is twice as effective as the linear branching one (Table 4). In the tip uptake scenario, the fungus with the nonlinear branching pattern is significantly more effective than the two other patterns with the anastomosis one being the least effective in later times (Fig. 10b; Table 4). While the anastomosis pattern has the advantage that it creates a well interconnected mycelium, anastomosis also results in the loss of tips so that P uptake is reduced.

Effectiveness of mycelium with respect to mycelial P uptake rate

| 2 days | 7 days | 14 days | 21 days |
---|---|---|---|---|

Full and half length uptake scenarios | ||||

Linear branching | 0.85 | 0.71 | 0.68 | 0.50 |

Nonlinear branching | 0.88 | 0.85 | 0.91 | 0.78 |

Anastomosis | 1 | 1 | 1 | 1 |

Tip uptake scenario | ||||

Linear branching | 0.49 | 0.45 | 0.43 | 0.42 |

Nonlinear branching | 1.00 | 1.00 | 1.00 | 1.00 |

Anastomosis | 0.54 | 0.38 | 0.20 | 0.17 |

## Discussion

This is the first mathematical model to quantify the effect of different AM fungal growth and uptake patterns on overall P influx into an arbuscular mycorrhizal root. It is a theoretical model study aimed to open the floor for a quantitative discussion about the processes involved in arbuscular mycorrhizal P uptake. Different conceptions about the processes involved in mycorrhizal P uptake that can be found in the literature are mechanistically represented in the model. Simulated soil depletion and P influx into a mycorrhizal root are largely different between the different scenarios. In order to verify or decline any of the hypotheses underlying these scenarios, the model needs to be validated with experimental data. While the modelling results obtained in the present study are in good agreement with data from a number of experimental studies in the literature, extrapolation to other AM fungal isolates of the species considered for the modelling here or to other AM fungal species and other experimental conditions has to be done with great caution. Using the model presented in this paper, we examined (a) the spatial acquisition of P by hyphae of arbuscular mycorrhizal fungi with different growth patterns, (b) the contribution of these hyphae to overall P influx into an arbuscular mycorrhizal root, and (c) assessed whether differences in uptake can be attributed to average structural features such as hyphal length densities.

### Comparing modelled soil depletion with literature results

Model results shown in Fig. 6 were in good agreement with experimental findings that mycorrhizal roots develop a depletion zone beyond the zone of root influence (Joner et al. 1995; Li et al. 1991a; Smith et al. 2000). Simulated depletion profiles for the full and half length uptake scenarios show that a fungus with an anastomosis growth pattern leaves a higher P concentration near the root surface while the fungi with the linear and nonlinear branching patterns deplete the soil in a more uniform way. The latter is qualitatively similar to the results of Li et al. (1991a) who measured a uniform P depletion in the hyphal compartment by *Glomus mosseae* associated with white clover. Joner et al. (1995) measured overall depletion of P from a hyphal compartment in an experiment with cucumber associated with either *Glomus invermaium* or *Glomus caledonium*. They found that the soil in the hyphal compartment of 1 cm width was depleted to 52–66% of the initial NaHCO_{3}-extractable P content. In Li et al. (1991b), the NaHCO_{3}-extractable P in a hyphal compartment of 2 cm width was depleted to approximately 25% of the initial value by *Glomus mosseae* associated with white clover. These literature values are not directly comparable with model results on soil P depletion because they have been measured in confined hyphal compartments of limited width. However, they suggest that the full and half length uptake scenarios with depletion between 13–66% of the initial content in the soil zone that contains hyphae are closer to experimentally observed results than the tip uptake scenario where the soil containing hyphae was only depleted to 97% of the initial P content.

### Comparing P inflow into a mycorrhizal root with literature results

Root inflow of P per unit length of root is calculated by multiplying root influx per unit root surface area with the root circumference. However, since our model is based on a planar root-soil interface, we can only estimate P inflow into a cylindrical root by assuming a value for the radius. Assuming a root radius of 0.2 mm, simulated root P inflow ranged between 15.08 and 1,118.41 fmol m^{−1} s^{−1}. Jakobsen et al. (1992a) give values of P inflow of 122–2,056 fmol m^{−1} s^{−1}. Published values of root P inflow into mycorrhizal plants on a whole-plant basis range from 300 to 12,000 fmol m^{−1} s^{−1} for mycorrhizal plants (Tinker and Nye 2000). However, one has to keep in mind that these experimentally obtained values for P inflow are generally obtained on a whole plant basis while or model results are on a single root basis. Methods for upscaling the model from single root to whole root system scale will enable more accurate comparisons between P inflow values measured on a whole root basis with simulated ones.

### Spatial P acquisition by external mycelium

P uptake rate per unit volume of soil due to the external mycelium at different distances from the root surface and at different times as shown in Fig. 7 allows assessing the spatial acquisition of P. Model results for the linear and nonlinear branching patterns in the tip uptake scenario show uniform P uptake rate over the whole colony. In contrast to this, model results of the full and half length uptake scenarios and also for the tip uptake scenario when exhibiting an anastomosis growth pattern, P uptake rate due to the AM fungi occurs mostly near the front of the spreading mycelium. This effect is particularly pronounced for the fungal species with the anastomosis pattern as the hyphal length density is highest at the mycelial front. This suggests that the anastomosis growth pattern would be the most effective fungal growth pattern in order to access P from a distance. Indeed, the *Acaulospora laevis* isolate used by Jakobsen et al. (1992a) that exhibited the anastomosis growth pattern was shown to be a particular good symbiont to access P from a distance as they were able to show in a follow-up study (Jakobsen et al. 1992b). The other two fungal growth patterns result in a higher hyphal length density near the root and thus hyphae compete with the root for P. Differences between AM fungi in spatial P uptake relative to the root surface are known (Drew et al. 2003; Jakobsen et al. 1992b; Jansa et al. 2005). So did Pearson and Jakobsen (1993) find that a strain of *Glomus caledonium* was most effective in accessing P from a distance compared to other fungal species. Smith et al. (2000) showed that a strain of *S. calospora* was less efficient to get ^{33}P from outside a root compartment than *G. caledonium*, but both fungi were equally effective with regard to total P uptake. Our model results could not reproduce experimental findings of Pearson and Jakobsen (1993) who found that the hyphal contribution to total P uptake of cucumber was small for *Scutellospora calospora*, but that root P uptake was improved due to root colonisation by *S. calospora*. Such a mechanism is currently not included in our model. We assume that differences in spatial P acquisition are solely attributable to the shape of the extraradical mycelium and the competition between roots and fungi. We did not include feedback mechanisms between AM root colonisation and P uptake on the one hand and root P uptake on the other hand. Such feedback mechanisms have however been suggested recently (Bucher 2007; Smith et al. 2004). Experimental data to quantify these feedback mechanisms are required in order to develop and parameterise such a model.

### Relative contribution of external mycelium to overall influx

The relative contributions of external mycelium and root to overall modelled P influx are shown in Fig. 9. P influx into the mycorrhizal root is dominated by the fungal mycelium in all uptake scenarios. However, in the tip uptake scenario, and in particular for the anastomosis growth pattern, roots contribute more considerably to overall influx. This means that in the full and half length uptake scenarios, we observe a “deactivation” of the root uptake pathway as suggested by Smith et al. (2003, 2004). Several reasons may be proposed for a massive reduction in direct P uptake into roots colonised by arbuscular mycorrhizal fungi. For example, the activity of P transporters located in root epidermal cells could be reduced as a response to AM fungal root colonisation (Smith et al. 2004). Under such a scenario, the root would not be able to take up P even if there was some available at the root surface. Although transporters are undoubtedly important, we observe this behaviour in our model results just by including P transport in soil and simultaneous uptake by AM fungal mycelium. Our results imply that extensive P depletion near the root due to the fungi may “deactivate” the direct uptake pathway via roots. In this model study this was the case for the linear and nonlinear branching patterns in the full and half length uptake scenarios.

### Conclusions and outlook

The different fungal uptake scenarios resulted in large differences between soil P depletion and P influx into a mycorrhizal root. The different fungal growth patterns resulted in differences in the spatial P acquisition by the fungal mycelium. Comparing model output with literature data suggests that the half length uptake scenario agrees best with experimental findings. The tip uptake scenario clearly underestimates soil P depletion due to the fungal mycelium and the full length uptake scenario seems to overestimate it. While our model results currently suggest that the tip uptake scenario is less efficient than the other two scenarios, including additional mechanisms happening at the tips, such as solubilising fixed forms of soil P, would probably consider this strategy more efficient.

*ρ*by a new variable

*ρ*

_{active}that represents the density of active hyphae. Secondly, the parameter

*d*in Eq. 6 can no longer be interpreted as the hyphal death rate, but taken to be the hyphal “inactivation rate”. Thirdly, we need to assume that hyphae are first inactivated and then inactive hyphae may degrade into the environment. We describe the density of inactive hyphae with

*ρ*

_{inactive}. This leads to the following model equations

*r*is the degradation rate of inactive hyphae. One could also add additional hyphal death into Eq. 13 to allow that active hyphae can either be deactivated or die directly.

The model presented in this paper could further be extended in order to explicitly model the plant carbon costs. The whole symbiosis including the bi-directional transfer of carbon and P, respectively, can be modelled. More experimental data to parameterise and validate such models are required. A more complex description of the architecture of the extraradical mycelium could for example distinguish between “runner hyphae”, the skeleton of the fungal colony, and “branched adsorbing structures” (BAS), small bunches of dichotomously branched hyphae formed by second and higher orders of runner hyphae (Bago et al. 1998). Bago (2000) suggested that BAS are the preferential site of hyphal P uptake. Including the findings of such morphological studies into the growth model for the external mycelium of AM fungi might lead to different simulated depletion zones and P uptake. However, the extension of the present fungal growth model to include BAS would require substantial changes to the model structure and we will address this in our future work. Further model extensions are related to the competition between several mycorrhizal roots and upscaling this single root model to the root system scale. Ongoing collaboration between modellers and experimentalists is currently examining mathematical multiscale methods for the purpose of upscaling from the single root to the root system scale. We expect that this work will also influence the upscaling of mycorrhizal roots.

## Footnotes

## Notes

### Acknowledgements

Andrea Schnepf is a Hertha-Firnberg Research Fellow (FWF Austrian Science Fund, Project T341-N13). Tiina Roose is a Royal Society University Research Fellow. We acknowledge two anonymous reviewers whose comments have truly strengthened this paper.

### Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

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