Research Article | Open Access
Louise Egerton-Warburton, "Aluminum-Tolerant Pisolithus Ectomycorrhizas Confer Increased Growth, Mineral Nutrition, and Metal Tolerance to Eucalyptus in Acidic Mine Spoil", Applied and Environmental Soil Science, vol. 2015, Article ID 803821, 9 pages, 2015. https://doi.org/10.1155/2015/803821
Aluminum-Tolerant Pisolithus Ectomycorrhizas Confer Increased Growth, Mineral Nutrition, and Metal Tolerance to Eucalyptus in Acidic Mine Spoil
Ectomycorrhizal fungi (ECM) may increase the tolerance of their host plants to Al toxicity by immobilizing Al in fungal tissues and/or improving plant mineral nutrition. Although these benefits have been demonstrated in in vitro (pure culture) or short-term nutrient solution (hydroponic) experiments, fewer studies have examined these benefits in the field. This study examined the growth, mineral nutrition, and Al levels in two Eucalyptus species inoculated with three Pisolithus ecotypes that varied in Al tolerance (in vitro) and grown in mine spoil in the greenhouse and field. All three ecotypes of Pisolithus improved Eucalyptus growth and increased host plant tolerance to Al in comparison to noninoculated plants. However, large variations in plant growth and mineral nutrition were detected among the Pisolithus-inoculated plants; these differences were largely explained by the functional properties of the Pisolithus inoculum. Seedlings inoculated with the most Al-tolerant Pisolithus inoculum showed significantly higher levels of N, P, Ca, Mg, and K and lower levels of Al than seedlings inoculated with Al-sensitive ecotypes of Pisolithus. These findings indicate an agreement between the fungal tolerance to Al in vitro and performance in symbiosis, indicating that both ECM-mediated mineral nutrient acquisition and Al accumulation are important in increasing the host plant Al tolerance.
Potentially toxic levels of aluminum (Al3+) are a major constraint to plant growth during the restoration of acidic mining soils. Exposure to Al generally results in a severe reduction in growth and productivity due to the inhibition of root cell division and elongation and reductions in the uptake of water and assimilation of nutrients including N, P, Ca, and Mg. Certain plant families show an innate tolerance to acidic soils and Al  and some trees species are thought to resist elevated soil metal concentrations by means of a large phenotypic plasticity . For many tree species, however, symbioses with a small guild of well-adapted ectomycorrhizal (ECM) fungi reduce the sensitivity of roots and plants to Al stress .
Many trees species form symbiotic associations with ECM fungi. These fungi provide nutrients and water to trees in exchange for carbohydrates and may also play a crucial role for tree regeneration in soils contaminated with metals. In vitro studies indicate that ECM fungi may tolerate high Al concentrations [4, 5] and show wide inter- and intraspecific variations in sensitivity to Al and other phytotoxic metals [6, 7]. For example, studies showed that Laccaria was more tolerant of high Al availability than Hebeloma or Lactarius [4, 8], and Pisolithus and Suillus were more tolerant of Al than Thelephora . In addition, tolerance may be correlated with soil metal concentrations at the site of origin  but not always .
In symbiosis, ECM fungi may show broad ameliorative effects on woody plant responses to acidification  and phytotoxic metals, including Al, Cu, Ni, and Zn [6, 11]. As a result, plants inoculated with ECM generally maintain better growth and reduced transfer of metals to shoots than nonmycorrhizal plants when exposed to acidity and/or an excess availability of Al . Such ECM-mediated metal tolerance has been attributed to various extracellular (chelation, cell-wall binding) or intracellular detoxification mechanisms such as binding to nonprotein thiols or vacuolar storage [1, 4, 11–14]. In other studies, however, the alleviation of Al or heavy metal toxicity by ECM was attributed to improved plant mineral nutrition owing to an increase in the uptake of poorly soluble ions (P) or base cations (Ca, Mg) [4, 10, 15, 16]. Further, the effects of ECM on plant Al tolerance may depend on the identity of the host species or ECM-host combination. For example, inoculation with Laccaria conferred Al tolerance to both Fagus and Pinus whereas inoculation with Paxillus conferred tolerance only to Pinus . In acidic soils, Xerocomus badius-Picea abies ECM showed a higher potential to store N, K, Mg, and metals in the fungal sheath than other ECM-Picea combinations .
Despite this increasing knowledge base, there are still surprisingly few field experiments that test for relevant differences in Al tolerance in ECM-host tree combination [4, 17]. Instead, most of the reported effects of ECM on Al toxicity and plant growth have been generated in short-term nutrient solution (hydroponic) experiments , and these results do not always accurately predict plant field performance . This study examined the growth and mineral nutrition of two Eucalyptus species inoculated with three Pisolithus ecotypes when grown in acid mine spoil in the greenhouse and field. The Pisolithus ecotypes were collected from coal mine spoil that differed in soil Al levels and were previously found to show varying levels of adaptive tolerance to Al . Pisolithus is a cosmopolitan genus that forms ECM associations with a broad range of angiosperm and gymnosperm tree species, including Eucalyptus . It is also a common pioneer on mine sites and increases plant growth in adverse soil conditions . The results were used to address three questions. (1) Do Pisolithus isolates from soils with the highest Al levels provide the greatest benefits to seedlings growing in mine spoil? (2) Does the effect of the Pisolithus isolates on plant growth vary with host plant identity? (3) If there is an effect of Pisolithus isolates on seedling growth, can this be attributed to reduced Al accumulation in plant tissues or improved plant nutrition?
2. Materials and Methods
Seed, inoculum, and soil for the pot trial were all sourced from the lease of Western Collieries Ltd., which is located in the Collie Coal Basin, Western Australia (33°26′S, 116°12′E). The Collie Coal Basin occurs in a significant physiognomic depression of the Darling Plateau in southwestern Australia. The region is typified by a warm Mediterranean-type climate and receives, on average, 993 mm precipitation per annum. Rainfall occurs from May to October (Southern Hemisphere winter-spring) followed by five to six months with little or no rainfall (Southern Hemisphere summer-autumn). Forest soils are typically nutrient poor leached sands (Table 1). In contrast, coal-mining soils are characterized by water repellence and composed of coarse nonbound sands with significant increases in the proportion of silt and clay in comparison to forest soils (Table 1). Mine spoil is also more acidic and contains higher levels of Al and Mn and lower levels of N, P, Ca, Mg, and K than forest soils (Table 1).
2.1. Pisolithus Inoculum Preparation
Eucalyptus seedlings were inoculated with cultures of Pisolithus previously identified as varying in Al tolerance . Briefly, Pisolithus was isolated from sporocarps collected under Eucalyptus trees in abandoned mine sites, restored sites, and native forest sites (Table 1) and sequentially cultured to produce pure culture. In vitro screening in Al-amended solid media identified variations in Al tolerance among the Pisolithus isolates, whereby Pisolithus that was isolated from abandoned and restored mine sites was highly tolerant of Al (as Al3+), and Pisolithus isolated from an adjacent native forest showed significantly lower tolerance to Al . Intersimple sequence repeat (ISSR) fingerprinting also revealed strong intraspecific variation among these Pisolithus isolates (Egerton-Warburton, unpublished data). These isolates were grown in bulk and then encapsulated in hydrogel beads  as this comprised an efficient method for the large-scale inoculation of containerized seedlings.
2.2. Greenhouse Trial
Two common forest trees used in restoration, Eucalyptus rudis Endl. and Eucalyptus patens Benth., were used in this study. Seeds of each species were collected from mature trees growing in abandoned mine sites on the lease of Western Collieries Ltd. at Collie. Half-sibling progeny was collected from an individual tree to reduce the effect of genetic variation within the seed stock on the trial. Seeds were surface sterilized with 3% v/v NaHClO4 for 5 min, washed in three changes of sterile deionized water, and then transferred to moistened sterile filter paper in petri dishes. Seeds were incubated in darkness at room temperature (20°C) for eight days before transplanting into prepared pots of mine spoil.
Mine spoil was used as the growing medium. These materials were classified as a sandy loam (73.8% sand; 16.2% clay; 10.1% silt), acidic (pH , mean ± s.e.), with high levels of Al ( μg g−1 soil) and low levels of plant-available P ( μg g−1 soil) and available moisture (6.8%–11%). Soils were sieved to 2 mm and then 1.5 kg was placed in each of 240 plastic pots lined with polythene bags that had been perforated at the base to allow drainage. Forty replicate pots per inoculum source plus 40 replicate pots of noninoculated pots (control) were established for each Eucalyptus species. For each species and inoculum source, four germinants were placed in an individual pot and supplied with eight hydrogel beads (two per plant) in the root zone. After planting, N and P fertilizers were applied once in solution to the soil surface at rates of 2 mg P kg−1 soil (as KH2PO4) and 2 mg N kg−1 soil (as NH4NO3). No further fertilizers were applied during the trial. Soils were watered to 8% soil moisture content and maintained in a greenhouse (30°C max, 21°C min). Pots were segregated by inoculum source to reduce the possibility of cross-contamination. At the four-leaf stage, seedlings were thinned to one per pot and any cotyledons were removed from seedlings to promote mycorrhization. Soil moisture levels were maintained by bringing pots to field capacity twice a week.
Seedlings were destructively harvested after 150 days of growth. At harvest, plants were washed gently from pots and divided into roots and shoots. Root material was subdivided into coarse and fine roots, with subsamples of fine roots from each treatment and species inspected for the abundance, color, and morphology of the colonising mycorrhizas. Short roots with fully developed sulfur yellow mantles and emanating hyphae were considered mycorrhizas of Pisolithus. Mycorrhizal colonization was expressed as the percentage of lateral fine roots colonized. The remaining root and shoot materials were dried to constant weight at 60°C and dry weights recorded. Subsamples of shoot material of each Eucalyptus and inoculum treatment were then ground to a fine powder and analyzed for N, P, K, Ca, Mg, and Al by CSBP and Farmers Analytical Laboratory (Bayswater, Western Australia; http://www.csbp-fertilisers.com.au/csbp-lab).
2.3. Field Trial
Seedlings of E. rudis and E. patens were inoculated with mine or forest site isolates of Pisolithus and assessed for growth and mycorrhization in the field. Seedlings inoculated with Pisolithus from the restored sites were not included in this comparison since the growth responses and nutrient levels were largely similar to those in seedlings grown with mine site inoculum (see Figure 1). In addition, noninoculated plants were not included in this assessment as their survival was extremely poor (<15%) in pot trials. Seeds were germinated as described previously. For each species and inoculum source, a single germinant was placed in an individual Jiffy pots (capacity 50 mL) containing sieved Collie topsoil, which is classed as sand (93% sand; 2.4% clay; 4.6% silt) with pH 5.3, extractable Al 2 μg g−1 soil, and P 1.6 μg g−1 soil. Seedlings were supplied with hydrogel bead (two per plant) in the root zone. Supplemental fertilization of forest soil was not required owing to the higher levels of plant-available P. Sixty-four seedlings of each species and inoculum type were established (total = 256 plants). Seedlings were maintained in a shade house and watered daily with an automatic watering system for four months prior to planting.
Seedlings were planted into a prepared rehabilitation site on the lease of Western Collieries Ltd. at Collie. The site had been prepared by battering the subsoil to a 9° slope followed by a dressing of local forest topsoil and a fertilizer application of 10 kg P ha−1 as single superphosphate (9% P). Eighteen months after planting, the surviving seedlings were excavated from the field site and processed for mycorrhizal colonization, root and shoot biomass, and mineral nutrient content as described previously (see Section 2.2 Greenhouse Trial).
2.4. Data Analyses
The differences in total plant biomass (root, shoot) and foliar mineral nutrient levels (pot, field trials) and mycorrhizal colonization (pot trial) were analyzed using analyzed linear mixed models with restricted maximum likelihood (REML) estimates. In the analyses, Eucalyptus host species and Pisolithus inoculation source (mine, restored, and forest) were specified as random effects. Because both host plant and mycorrhizal partner can have large influences on host nutrition, the relative contribution of Eucalyptus host species and Pisolithus inoculum source on plant mineral nutrition was tested using REML linear models. Biomass accumulation was modeled as a function of the fixed effect of plant nutrient levels (N, P, K, Ca, Mg, and Al), with Eucalyptus host and Pisolithus source specified as random effects. To determine the combinations of nutrients with the greatest explanatory power, each variable (mineral nutrient) was added into the model in a stepwise fashion. Briefly, variables that were found to be significant in the presence of previously fitted variables were retained in the model, while variables that were no longer significant in the presence of other variables were removed. The final combined models were used to report the variance explained by plant host and inoculum source in the pot and field trials. In addition, variables retained in the model were tested using post hoc multiple -tests to determine significant differences in mineral nutrients between plant hosts or inoculum sources. All variables were tested for normality and, where necessary, log transformations were applied prior to analysis.
3.1. Greenhouse Trial
Eucalyptus host () influenced plant root and shoot biomass accumulation whereby E. rudis plants were significantly larger than E. patens plants (Figure 1(b)). Shoot biomass in E. patens and E. rudis was significantly higher (; Figure 1(a)) in inoculated than in noninoculated (control) plants, but there was no difference in shoot biomass among Pisolithus sources (). Root biomass in E. patens and E. rudis was also significantly higher (; Figure 1(b)) in inoculated than in noninoculated (control) plants. In E. patens, there was no significant difference in root biomass among Pisolithus sources () whereas E. rudis inoculated with Pisolithus from mine sites produced significantly greater root biomass than when inoculated with Pisolithus from restored or forest sites ().
Both Eucalyptus host () and Pisolithus source () influenced mycorrhizal root colonization (Figure 1(c)). Root colonization was significantly higher in E. rudis (%; mean ± s.e.) than E. patens (%). In addition, % root tips were colonized in plants inoculated with mine site Pisolithus compared with % for restored site and % for forest site Pisolithus. There was no significant Eucalyptus x Pisolithus source interaction ().
Results from REML (Table 2) revealed that variations in plant N, P, and Ca (positive) and Al content (negative) significantly influenced biomass accumulation, and such variations were largely explained (68.4%) by the functional properties of the Pisolithus inoculum. Seedlings inoculated with mine or restored site Pisolithus inoculum showed significantly higher levels of N, P, and Ca, and lower levels of Al than seedlings inoculated with forest site Pisolithus (; Figures 2(a), 2(b), 2(d), and 2(f)). Noninoculated seedlings contained the lowest levels of mineral nutrients and highest levels of Al. Levels of K and Mg were also significantly higher in seedlings inoculated with mine or restored site than forest site Pisolithus (; Figures 2(c) and 2(e), resp.), but these nutrients were not significant in REML models of biomass accumulation.
3.2. Field Trial
Eucalyptus host () and Pisolithus source () influenced plant biomass accumulation after 18 months in the field (Figure 3(a)). There was no significant Eucalyptus x Pisolithus source interaction (). Eucalyptus rudis was significantly larger than E. patens, and Pisolithus from mine sites resulted in greater plant biomass than Pisolithus from the forest site.
Overall levels of ECM root colonization did not differ significantly between seedlings receiving mine site (%; mean ± s.e.) or forest sources of Pisolithus (%). However, five different morphological types of ECM, including Pisolithus, colonized root tips. Pisolithus was readily identified by the presence of a coarse, sulfur yellow mantle, emanating hyphae, and rhizomorphs. One ECM was consistent with Cenococcum (black mantle, short black hyphae), while the other was an unknown type characterized by a deep brown mantle and short radiating external hyphae. In fact, after 18 months of field growth, Pisolithus mycorrhizas comprised, on average, only % of ECM root tips in seedlings receiving mine site inoculum and % of ECM root tips in seedlings receiving forest inoculum.
Results from REML analyses for field-grown plants were similar to those from the pot trial: variations in plant N, P, Ca, and Mg (positive) and Al (negative) influenced plant biomass accumulation (Table 2). In addition, these variations were better explained by the properties of the Pisolithus inoculum (58.6%) than host plant. Plant N levels were significantly higher in seedlings inoculated with mine ( mg N plant−1; mean ± s.e.) than forest site Pisolithus ( mg N plant−1; ). In addition, levels of plant K (), Ca (), Mg (), and P () were significantly higher, and Al levels were significantly lower () in plants inoculated with mine than forest site Pisolithus (Figure 3(b)).
An extensive literature has shown that ECM fungi from metal-contaminated soils may present a higher metal tolerance (in vitro) than isolates from noncontaminated soils and that intraspecific variation in metal tolerance can occur among isolates [3, 6, 7, 9]. However, questions have remained about whether the adaptive metal tolerance observed in vitro might result in increased protection against metal toxicity in a host plant growing in contaminated soils. In this study, all three ecotypes of Pisolithus improved Eucalyptus growth and mineral nutrition (N, P, Ca, Mg, and K) and reduced the transfer to a phytotoxic metal (Al) to the host plant in comparison to nonmycorrhizal seedlings. These trends are in general agreement with earlier studies of ECM plants in metal-contaminated and native soils [3, 11, 15]. More notably, the experiments revealed that the source of the Pisolithus isolate was the largest influence of plant growth, mineral nutrition, and Al content.
Overall, Eucalyptus seedlings inoculated with mine Pisolithus produced the largest growth responses and forest Pisolithus the least. The magnitude of this effect is most obvious in E. rudis (pot trial) and in shoot biomass accumulation in the field trial (both Eucalyptus species). Because the study used half-sib progeny and confined plant growth to a single substrate (mine spoil), these results suggest that genetic differences existed between Pisolithus isolates in their ability to benefit seedling growth [3, 6, 21]. In addition, plant growth responses were largely consistent with the patterns of Pisolithus Al tolerance reported in in vitro experiments , suggesting a reasonable agreement between the fungal sensitivity to specific metals in vitro and performance in symbiosis in acidic mine spoil (Question ).
Even so, there were large variations in the symbiotic and physiological effectiveness of Pisolithus between host species: E. rudis showed high levels of mycorrhizal root colonization and correspondingly larger growth responses to Pisolithus in comparison to E. patens (Question ). This result is not surprising given the wide range of physiological responses that have been reported in host species inoculated with Pisolithus [22, 23]. What was surprising, however, was that all three isolates of Pisolithus produced similar root and shoot growth responses in E. patens (pot trial). While it is possible, this result represents some form of fungal-host incompatibility between Pisolithus and E. patens [21, 23], the more likely explanation is that Pisolithus acted as a strong C sink during the early stages of the symbiosis . Eucalyptus patens grown with mine site Pisolithus for 4 months (pot trial) showed the highest levels of root colonization but limited biomass accumulation. After 18 months of field growth, however, root colonization and seedling biomass in E. patens were similar to E. rudis. These results support the idea that early symbiosis may have acted as a temporary C sink in E. patens.
At least two general types of mechanisms apparently contributed to the enhanced growth response in E. rudis with mine site Pisolithus (Question ). The most obvious was the ability of the ECM partner to reduce Al levels within the plant. In plants grown with mine site Pisolithus, Al levels remained low in comparison to plants grown with forest Pisolithus. These experiments were not intended to evaluate the specific mechanisms by which ECM fungi might alleviate Al toxicity. However, the significant differences in foliar Al levels between nonmycorrhizal and Pisolithus-inoculated plants indicate that mycorrhizal structures may have limited Al penetration into the root symplasm and subsequent transport to the shoot [11, 25]. Binding of Al to the fungal cell walls represented a substantial fraction of the metal accumulated by Pisolithus mycorrhizas on Eucalyptus  and Pinus  and may well be part of the mechanism by which ECM Eucalyptus tolerated the high levels of the metal in spoil in the current study. In addition, studies with Pisolithus and other ECM fungi have highlighted a role for Al detoxification within the fungal vacuole with S-rich substrates or P-rich granules [12–14, 27] and the capacity of Pisolithus mycelia to produce low molecular-weight organic acids that bind Al and prevent its absorption [4, 25, 28]. Although it is uncertain which processes might be involved, the reduction in Al levels in ECM Eucalyptus in this study implies an efficient and substantial tolerance mechanism.
A second type of tolerance mechanism appeared to be the maintenance of nutrient acquisition. Mycorrhizal E. rudis contained significantly higher levels of N, P, K, Ca, and Mg than nonmycorrhizal plants in mine spoil. This is particularly important because mine spoil is largely deficient in essential plant nutrients such as N, P, and K, and high levels of Al are known to limit the uptake of divalent cations (Ca, Mg). Indeed, the stunted root growth and low levels of foliar N, P, K, Ca, and Mg in nonmycorrhizal E. rudis and E. patens were consistent with Al-induced growth impairments in woody plants  and competitive inhibition of Mg and Ca uptake [16, 29]. In contrast, plants grown with Pisolithus showed substantial increases in N and P, consistent with the physiological role of ECM in natural forest or Al-treated soils [4, 10, 25], as well as increased plant Mg, Ca, and K levels. This result suggests that an ECM-mediated uptake of cations might directly ameliorate the effects of Al [4, 8, 16] in a manner similar to other phytotoxic metals [11, 15], or indirectly by enhancing P uptake . Taken together with plant Al levels, these findings suggest that both plant nutrient imbalances and direct Al toxicity are likely the main reasons for the negative effects of mine spoil on plant growth.
It is interesting to note that inoculation with mine site Pisolithus resulted in the greatest increases in plant growth and nutrient status, and forest Pisolithus resulted in the smallest increases. This outcome agrees with earlier findings showing the high intraspecific variability of Pisolithus (and other ECM fungi) to promote the mineral nutrition of the host plant [21, 22, 31]. However, other key factor(s) besides nutrient acquisition may be involved. Pisolithus produces long distance exploration hyphae with hydrophobic cell walls that are capable of transporting physiologically significant quantities of water through the soil-plant continuum . This is notable because mine spoil shows low water holding capacity, and juvenile Eucalyptus growth is strongly and negatively influenced by soil moisture deficits. The inoculation of woody plants with Pisolithus has been shown to mitigate the effects of drought by improving water acquisition or modifying plant ecophysiological responses to soil moisture deficits . Because genotypes of Pisolithus differ markedly in their capacity to confer drought tolerance to their host , it is tempting to speculate that Pisolithus, and especially the mine site isolate, may have enhanced the growth of E. rudis by ameliorating the effects of soil moisture deficits. Given the potential importance of this mechanism, further field-based experimentation is needed to determine the impact of the different Pisolithus isolates on Eucalyptus ecophysiology.
Inoculation with Pisolithus appeared to compensate for inefficient plant nutrient acquisition as well as bestow increased Al resistance in a host plant that showed a level of sensitivity to spoil conditions. Pisolithus isolates also differed markedly in their capacity to confer such benefits to their host indicating that screening and selecting fungal isolates based on their capacity to adapt to abiotic stresses in the spoil, such as Al, may be a prerequisite to using ECM isolates for larger scale inoculation trials or restoration. Although the potential exists to utilize the most Al-tolerant ECM, it was also clear that not all Eucalyptus species would benefit from inoculation during early seedling establishment. As a result, screening the performance of various Pisolithus-Eucalyptus species combinations in mine spoil comprises a logical second step in planning for future field planting.
Conflict of Interests
The author declares that there is no conflict of interests regarding the publication of this paper.
This work was supported by a Commonwealth Forestry Postgraduate Award and Western Collieries Ltd. (WCL). The author thanks Bob Brierley (WCL) for assistance with site selection and seedling outplanting and Dr. Clem Kuek for creating the hydrogel beads used for inoculation.
- I. Brunner and C. Sperisen, “Aluminum exclusion and aluminum tolerance in woody plants,” Frontiers in Plant Science, vol. 4, article 172, 2013.
- D. M. Wilkinson and N. M. Dickinson, “Metal resistance in trees: the role of mycorrhizae,” Oikos, vol. 72, no. 2, pp. 298–300, 1995.
- J. V. Colpaert, J. H. L. Wevers, E. Krznaric, and K. Adriaensen, “How metal-tolerant ecotypes of ectomycorrhizal fungi protect plants from heavy metal pollution,” Annals of Forest Science, vol. 68, no. 1, pp. 17–24, 2011.
- U. Ahonen-Jonnarth, A. Göransson, and R. D. Finlay, “Growth and nutrient uptake of ectomycorrhizal Pinus sylvestris seedlings in a natural substrate treated with elevated Al concentrations,” Tree Physiology, vol. 23, no. 3, pp. 157–167, 2003.
- G. W. Thompson and R. J. Medve, “Effects of aluminum and manganese on the growth of ectomycorrhizal fungi,” Applied and Environmental Microbiology, vol. 48, pp. 556–560, 1984.
- J. Hartley, J. W. G. Cairney, and A. A. Meharg, “Do ectomycorrhizal fungi exhibit adaptive tolerance to potentially toxic metals in the environment?” Plant and Soil, vol. 189, no. 2, pp. 303–319, 1997.
- D. Blaudez, C. Jacob, K. Turnau et al., “Differential responses of ectomycorrhizal fungi to heavy metals in vitro,” Mycological Research, vol. 104, no. 11, pp. 1366–1371, 2000.
- R. H. Jongbloed and G. W. F. H. Borst-Pauwels, “Effects of aluminium and pH on growth and potassium uptake by three ectomycorrhizal fungi in liquid culture,” Plant and Soil, vol. 140, no. 2, pp. 157–165, 1992.
- L. M. Egerton-Warburton and B. J. Griffin, “Differential responses of Pisolithus tinctorius isolates to aluminum in vitro,” Canadian Journal of Botany, vol. 73, no. 8, pp. 1229–1233, 1995.
- R. Finlay, “Interactions between soil acidification, plant growth and nutrient uptake in ectomycorrhizal associations of forest trees,” Ecological Bulletins, vol. 44, pp. 197–214, 1995.
- G. Jentschke and D. L. Godbold, “Metal toxicity and ectomycorrhizas,” Physiologia Plantarum, vol. 109, no. 2, pp. 107–116, 2000.
- I. Kottke, X. M. Qian, K. Pritsch, I. Haug, and F. Oberwinkler, “Xerocomus badius—Picea abies, an ectomycorrhiza of high activity and element storage capacity in acidic soil,” Mycorrhiza, vol. 7, no. 5, pp. 267–275, 1998.
- H. Bücking, S. Beckmann, W. Heyser, and I. Kottke, “Elemental contents in vacuolar granules of ectomycorrhizal fungi measured by EELS and EDXS. A comparison of different methods and preparation techniques,” Micron, vol. 29, no. 1, pp. 53–61, 1998.
- F. Martin, P. Rubini, R. Côté, and I. Kottke, “Aluminium polyphosphate complexes in the mycorrhizal basidiomycete Laccaria bicolor: a 27Al-nuclear magnetic resonance study,” Planta, vol. 194, no. 2, pp. 241–246, 1994.
- P. Jourand, L. Hannibal, C. Majorel, S. Mengant, M. Ducousso, and M. Lebrun, “Ectomycorrhizal Pisolithus albus inoculation of Acacia spirorbis and Eucalyptus globulus grown in ultramafic topsoil enhances plant growth and mineral nutrition while limits metal uptake,” Journal of Plant Physiology, vol. 171, no. 2, pp. 164–172, 2014.
- J. Bose, O. Babourina, and Z. Rengel, “Role of magnesium in alleviation of aluminium toxicity in plants,” Journal of Experimental Botany, vol. 62, no. 7, pp. 2251–2264, 2011.
- D. H. Marx and J. D. Artmann, “Pisolithus tinctorius ectomycorrhizae improve survival and growth of pine seedlings in acid coal spoils in Kentucky and Virginia,” Reclamation Review, vol. 2, pp. 23–31, 1979.
- P. H. Nygaard and H. A. de Wit, “Effects of elevated soil solution Al concentrations on fine roots in a middle-aged Norway spruce (Picea abies (L.) Karst.) stand,” Plant and Soil, vol. 265, no. 1-2, pp. 131–140, 2004.
- F. Martin, J. Díez, B. Dell, and C. Delaruelle, “Phylogeography of the ectomycorrhizal Pisolithus species as inferred from nuclear ribosomal DNA ITS sequences,” New Phytologist, vol. 153, no. 2, pp. 345–357, 2002.
- C. Kuek, I. Tommerup, and N. Malajczuk, “Hydrogel bead inocula for the production of ectomycorrhizal eucalypts for plantations,” Mycological Research, vol. 96, no. 4, pp. 273–277, 1992.
- T. Burgess, B. Dell, and N. Malajczuk, “Variation in mycorrhizal development and growth stimulation by 20 Pisolithus isolates inoculated on to Eucalyptus grandis W.Hill ex Maiden,” New Phytologist, vol. 127, no. 4, pp. 731–739, 1994.
- T. I. Burgess, N. Malajczuk, and T. S. Grove, “The ability of 16 ectomycorrhizal fungi to increase growth and phosphorus uptake of Eucalyptus globulus Labill. and E. diversicolor F. Muell,” Plant and Soil, vol. 153, no. 2, pp. 155–164, 1993.
- J. W. G. Cairney, “Intraspecific physiological variation: implications for understanding functional diversity in ectomycorrhizal fungi,” Mycorrhiza, vol. 9, no. 3, pp. 125–135, 1999.
- J. W. Cairney, A. E. Ashford, and W. G. Allaway, “Distribution of photosynthetically fixed carbon within root systems of Eucalyptus pilularis plants ectomycorrhizal with Pisolithus tinctorius,” New Phytologist, vol. 112, no. 4, pp. 495–500, 1989.
- J. R. Cumming and L. H. Weinstein, “Aluminum-mycorrhizal interactions in the physiology of pitch pine seedlings,” Plant and Soil, vol. 125, no. 1, pp. 7–18, 1990.
- K. Moyer-Henry, I. Silva, J. Macfall et al., “Accumulation and localization of aluminium in root tips of loblolly pine seedlings and the associated ectomycorrhiza Pisolithus tinctorius,” Plant, Cell & Environment, vol. 28, no. 2, pp. 111–120, 2005.
- K. Turnau, I. Kottke, and F. Oberwinkler, “Element localization in mycorrhizal roots of Pteridium aquilinum (L.) Kuhn collected from experimental plots treated with cadmium dust,” New Phytologist, vol. 123, no. 2, pp. 313–324, 1993.
- K. Tahara, M. Norisada, T. Tange, H. Yagi, and K. Kojima, “Ectomycorrhizal association enhances Al tolerance by inducing citrate secretion in Pinus densiflora,” Soil Science and Plant Nutrition, vol. 51, no. 3, pp. 397–403, 2005.
- L. van Schöll, W. G. Keltjens, E. Hoffland, and N. van Breemen, “Effect of ectomycorrhizal colonization on the uptake of Ca, Mg and Al by Pinus sylvestris under aluminium toxicity,” Forest Ecology and Management, vol. 215, no. 1–3, pp. 352–360, 2005.
- H. Bücking, “Phosphate absorption and efflux of three ectomycorrhizal fungi as affected by external phosphate, cation and carbohydrate concentrations,” Mycological Research, vol. 108, no. 6, pp. 599–609, 2004.
- M. S. Lamhamedi, P. Y. Bernier, and J. A. Fortin, “Growth, nutrition and response to water stress of Pinus pinaster inoculated with ten dikaryotic strains of Pisolithus sp,” Tree Physiology, vol. 10, no. 2, pp. 153–167, 1992.
- M. S. Lamhamedi and J. A. Fortin, “Genetic variations of ectomycorrhizal fungi: extramatrical phase of Pisolithus sp,” Canadian Journal of Botany, vol. 69, no. 9, pp. 1927–1934, 1991.
Copyright © 2015 Louise Egerton-Warburton. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.