Can herbivores sharing the same host plant be mutualists?

Resource partitioning is considered to be a prerequisite for coexisting species to evolve from competition to mutualism. This is uniquely different for two major pest insects of rice. These herbivores preferentially opt to coinfest the same host plants, and through plant-mediated mechanisms, cooperatively utilize these plants in a mutualistic manner.     

Can hypodermal passage cell distribution limit root penetration by mycorrhizal fungi?

* The basis for significant interspecific variability in colonization by arbuscular mycorrhizal fungi is poorly understood. Limited evidence suggests that, for species with a dimorphic hypodermis, colonization of the root cortex occurs only through hypodermal passage cells. Therefore, the hypothesis that interspecific variability in mycorrhizal colonization is accounted for by interspecific variation in passage cell distribution was tested. * The arbuscular mycorrhizal colonization and distribution of fungal penetration points and hypodermal passage cells in the root systems of eight species (seven plant families) possessing a dimorphic hypodermis were characterized. * Mycorrhizal fungal penetration of the hypodermis occurred exclusively through passage cells. Moreover, the proportion of root length with passage cells explained nearly 99% of the variability among the eight plant species in the proportion of root length with penetration points. * In dimorphic hypodermal species, passage cells appear to be key determinants of mycorrhizal colonization because they are the cells through which fungal penetration of the hypodermis occurs. Variation among such species in mycorrhizal colonization may be at least partly determined by variation in the proportion of root length with passage cells.     

The effect of host mycorrhizal status on host plant–parasitic plant interactions

Two pot experiments were conducted to examine three-level interactions between host plants, mycorrhizal fungi and parasitic plants. In a greenhouse experiment, Poa annua plants were grown in the presence or absence of an AM fungus (either Glomus lamellosum V43a or G. mosseae BEG29) and in the presence or absence of a root hemiparasitic plant (Odontites vulgaris). In a laboratory experiment, mycorrhizal infection (Glomus claroideum BEG31) of Trifolium pratense host plants (mycorrhizal versus non-mycorrhizal) was combined with hemiparasite infection (Rhinanthus serotinus) of the host (parasitized versus non-parasitized). Infection with the two species of Glomus had no significant effect on the growth of P. annua, while hemiparasite infection caused a significant reduction in host biomass. Mycorrhizal status of P. annua hosts (i.e. presence/absence of AM fungus) affected neither the biomass nor the number of flowers produced by the attached O. vulgaris plants. Infection with G. claroideum BEG31 greatly increased the biomass of T. pratense, but hemiparasite infection had no effect. The hemiparasitic R. serotinus plants attached to mycorrhizal hosts had higher biomass and produced more flowers than plants growing with non-mycorrhizal hosts. Roots of T. pratense were colonized by the AM fungus to an extent independent of the presence or absence of the hemiparasite. Our results confirm earlier findings that the mycorrhizal status of a host plant can affect the performance of an attached root hemiparasite. However, improvement of the performance of the parasitic plant following attachment to a mycorrhizal host depends on the extent to which the AM fungi is able to enhance the growth of the host. Accepted: 23 February 2001     

When do arbuscular mycorrhizal fungi protect plant roots from pathogens?

Arbuscular mycorrhizal (AM) fungi are mainly thought to facilitate phosphorus uptake in plants, but they can also perform several other functions that are equally beneficial. Our recent study sheds light on the factors determining one such function, enhanced plant protection from root pathogens. Root infection by the fungal pathogen Fusarium oxysporum was determined by both plant susceptibility and the ability of an AM fungal partner to suppress the pathogen. The non-susceptible plant species (Allium cepa) had limited F. oxysporum infection even without AM fungi. In contrast, the susceptible plant species (Setaria glauca) was heavily infected and only AM fungi in the family Glomeraceae limited pathogen abundance. Plant susceptibility to pathogens was likely determined by contrasting root architectures between plants, with the simple rooted plant (A. cepa) presenting fewer sites for infection. AM fungal colonization, however, was not limited in the same way in part because plants with fewer, simple roots are more mycorrhizal dependent. Protection only by Glomus species also indicates that whatever the mechanism(s) of this function, it responds to AM fungal families differently. While poor at pathogen protection, AM fungal species in the family Gigasporaceae most benefited the growth of the simple rooted plant species. Our research indicates that plant trait differences, such as root architecture can determine how important each mycorrhizal function is to plant growth but the ability to provide these functions differs among AM fungi.Key words: arbuscular mycorrhizal fungi, Fusarium oxysporum, root architecture, pathogen protection, multi-functionalityArbuscular mycorrhizas (AM) represent the oldest and most widespread symbiosis with land plants.¹ Most mycorrhizal research has focused on the ability of AM fungi to facilitate nutrient uptake, particularly phosphorus.² Although researchers recognize that AM fungi are multi-functional,³ it is not clear what factors determine which function an AM fungus performs or its relative importance to the plant.⁴ Newsham et al. (1995)³ hypothesized that AM function is based on root architecture: plants with simple rooting systems are dependent on mycorrhizas for nutrient uptake, while those with complex root systems are less dependent on mycorrhizas for nutrient uptake, but are more susceptible to root pathogens because of increased numbers of infections sites.³ These two functions, phosphorus uptake and enhanced pathogen protection from mycorrhizas also depend on the identity of the fungus. Arbuscular mycorrhizal fungi in the family Gigasporaceae are more effective at enhancing plant phosphorus, while AM fungi in the Glomeraceae better protect plants from root pathogens.⁵Our results support both plant and fungal control of a common pathogen, Fusarium oxysporum, and the interaction between these two factors ultimately determined the level of pathogen infection and plant mycorrhizal benefit. We inoculated two plant species that have contrasting root architectures with one of six AM fungal species from two families (or no AM fungi). After five months of growth, plants were inoculated with F. oxysporum, grown for another month and then harvested. All plant seeds and fungi were collected in a local old field community.⁶ Allium cepa (garden onion) was not susceptible to F. oxysporum likely because it has only a few adventitious roots below the main bulb that do not present many sites for infection. In contrast, Setaria glauca (yellow foxtail) was heavily infected by F. oxysporum and has fine roots with increased numbers of branching points and lateral meristems where fungi can colonize.⁷ For the susceptible plant (S. glauca), AM fungal species from the family Glomeraceae were effective at reducing pathogen abundance while species from the Gigasporaceae were not. Forming a symbiosis with a Glomus species resulted in S. glauca plants that were as large as control plants. AM fungal species from the family Gigaspoaceae were more beneficial to growth of the simple rooted A. cepa, which had fewer roots to take up soil nutrients.Reduced rooting structures may limit pathogen infection sites, but AM fungal colonization was not limited in the same way and may actually alter plant root architecture. While the simple rooted A. cepa had limited pathogen susceptibility, it had twice the AM fungal colonization of the complex rooted S. glauca. Because the simple rooted plant has a greater dependence on mycorrhizas,⁸ it likely transmits chemical signals to rapidly initiate mycorrhizal formation,⁹ but then may have less control on the spread of AM fungi within the root. In contrast, S. glauca is more susceptible to fungal pathogens and may be less mycorrhizal dependent in nature.¹⁰ As a result, S. glauca may treat all colonizing root fungi as potential parasites. Colonization by AM fungi from the Glomeraceae was also much greater than those in the Gigasporaceae due to differences in fungal life history strategy between these families.^11,12 AM fungal colonization can reduce root branching in plants and alter plant allocation to roots, thereby increasing mycorrhizal dependence for nutrients^10,13 and potentially reducing pathogen infection sites. Mycorrhizal induced changes to plant root architecture may therefore reinforce current mycorrhizal associations and alter future fungal colonization attempts.¹⁴ An important next step is to test if AM fungal families (or species) alter plant root architecture in different ways and the degree to which these effects depend on colonization timing and the plant host.Our study did not isolate the particular mechanism by which AM fungi control pathogens, but this mechanism clearly differentiates between AM fungal families. AM fungi can control pathogens through several mechanisms including direct competition for colonization sites, indirect initiation of plant defensive responses or altering other rhizosphere biota.¹⁵ Although these AM fungal families differ in the intensity of root colonization,¹¹ percentage of root length colonized by an AM fungus is a poor predictor of pathogen limitation compared to family identity,^12,16 suggesting that direct competition for space is unlikely. AM fungi share many cell surface molecules with pathogenic fungi like Fusarium.¹⁷ These molecules can act as signals that initiate plant production of defensive compounds such as phytoalexins, phenolics and other compounds.¹⁸ While AM fungi appear to evade these defenses, only AM fungal species in the family Glomeraceae would have elicited plant responses which altered future infection by F. oxysporum. AM fungi in the Gigasporaceae may differ more from F. oxysporum in their chemical signals or not colonize roots sufficiently to induce a sustained, system-wide plant response. In addition, many rhizosphere related microbes are antagonistic to pathogenic fungi¹⁵ and may differ in their response to the different AM fungal families.¹⁹ Because rhizosphere microbes also differ among plant species, plant pathogen protection may be influenced by multiple ecological interactions that determine the specific cases when mycorrhizal pathogen protection occurs. To distinguish between these mechanisms, future experiments could test whether biochemical similarity or ecological similarity (especially with other soil biota) between an AM fungus and fungal pathogen can predict mycorrhizal induced pathogen protection.Plant and fungal identity clearly affect AM fungal function and benefit, but to accurately use AM fungi in agriculture and restoration^20,21 we must clearly understand how functional mechanisms differ. Different mycorrhizal functions may be based on common plant traits like root architecture, but ecology, colonization timing and environment may alter the specific function AM fungi provide and its importance to plants. While it may be useful to establish greenhouse rules about which fungal species perform specific mycorrhizal functions, predicting their role in more complex systems relies on understanding if other factors will enhance or negate these effects. Most AM fungal species vary in their ability to perform each function and these can be locally adapted to limiting soil nutrients.²² In plants, there is also a range to which specific mycorrhizal functions may benefit plant fitness, and these responses are based on both plant traits (which change throughout a plant''s life cycle) and the local environment.^23,24 Given this variation, it is critical to understand if AM fungi can respond to cues from the plant or the environment to identify what factors limit plant growth and whether a the most effective AM fungus shows a greater response.     

Does responsiveness to arbuscular mycorrhizal fungi depend on plant invasive status?

Differences in the direction and degree to which invasive alien and native plants are influenced by mycorrhizal associations could indicate a general mechanism of plant invasion, but whether or not such differences exist is unclear. Here, we tested whether mycorrhizal responsiveness varies by plant invasive status while controlling for phylogenetic relatedness among plants with two large grassland datasets. Mycorrhizal responsiveness was measured for 68 taxa from the Northern Plains, and data for 95 taxa from the Central Plains were included. Nineteen percent of taxa from the Northern Plains had greater total biomass with mycorrhizas while 61% of taxa from the Central Plains responded positively. For the Northern Plains taxa, measurable effects often depended on the response variable (i.e., total biomass, shoot biomass, and root mass ratio) suggesting varied resource allocation strategies when roots are colonized by arbuscular mycorrhizal fungi. In both datasets, invasive status was nonrandomly distributed on the phylogeny. Invasive taxa were mainly from two clades, that is, Poaceae and Asteraceae families. In contrast, mycorrhizal responsiveness was randomly distributed over the phylogeny for taxa from the Northern Plains, but nonrandomly distributed for taxa from the Central Plains. After controlling for phylogenetic similarity, we found no evidence that invasive taxa responded differently to mycorrhizas than other taxa. Although it is possible that mycorrhizal responsiveness contributes to invasiveness in particular species, we find no evidence that invasiveness in general is associated with the degree of mycorrhizal responsiveness. However, mycorrhizal responsiveness among species grown under common conditions was highly variable, and more work is needed to determine the causes of this variation.     

Can the negative plant–soil feedback of Jacobaea vulgaris be explained by autotoxicity?

Field and bioassay studies with Jacobaea vulgaris (ragwort) have shown that plants grow poorly in soil originating from the rhizosphere of this species and that this can influence the dynamics of ragwort populations during secondary succession. In the present study we examined whether the negative effect of ragwort on conspecifics may be due to autotoxicity. First, we experimentally established that ragwort exerts negative plant–soil feedback. We subsequently examined the inhibitory effects on germination and seedling performance of different strengths of aqueous extracts made from shoot and root tissues of ragwort, and from soil in which ragwort had been growing. The effects of the extracts were tested for seedlings growing in sterilised soil or in glass beads with water. Finally, the inhibitory effect of entire root fragments on seedling performance was tested. We observed that performance of seedlings growing in glass beads was significantly reduced by the high and medium strength root and shoot extracts. Extracts made from soil did not differ significantly from the control, and seedlings growing in sterilised soil were also not affected by ragwort extracts. Seed germination was significantly reduced by the high strength shoot extract only. The root length of seedlings growing in water with root fragments was reduced significantly. We conclude that under laboratory conditions ragwort can be autotoxic and discuss the role that autotoxicity may play in influencing the dynamics of ragwort populations during secondary succession.     

Are carbon and nitrogen exchange between fungi and the orchid Goodyera repens affected by irradiance?

Background and Aims The green orchid Goodyera repens has been shown to transfer carbon to its mycorrhizal partner, and this flux may therefore be affected by light availability. This study aimed to test whether the C and N exchange between plant and fungus is dependent on light availability, and in addition addressed the question of whether flowering and/or fruiting individuals of G. repens compensate for changes in leaf chlorophyll concentration with changes in C and N flows from fungus to plant.Methods The natural abundances of stable isotopes of plant C and N were used to infer changes in fluxes between orchid and fungus across natural gradients of irradiance at five sites. Mycorrhizal fungi in the roots of G. repens were identified by molecular analyses. Chlorophyll concentrations in the leaves of the orchid and of reference plants were measured directly in the field.Key Results Leaf δ¹³C values of G. repens responded to changes in light availability in a similar manner to autotrophic reference plants, and different mycorrhizal fungal associations also did not affect the isotope abundance patterns of the orchid. Flowering/fruiting individuals had lower leaf total N and chlorophyll concentrations, which is most probably explained by N investments to form flowers, seeds and shoot.Conclusions The results indicate that mycorrhizal physiology is relatively fixed in G. repens, and changes in the amount and direction of C flow between plant and fungus were not observed to depend on light availability. The orchid may instead react to low-light sites through increased clonal growth. The orchid does not compensate for low leaf total N and chlorophyll concentrations by using a ¹³C- and ¹⁵N-enriched fungal source.     

Can plant resistance to specialist herbivores be explained by plant chemistry or resource use strategy?

At both a macro- and micro-evolutionary level, selection of and performance on host plants by specialist herbivores are thought to be governed partially by host plant chemistry. Thus far, there is little evidence to suggest that specialists can detect small structural differences in secondary metabolites of their hosts, or that such differences affect host choice or performance of specialists. We tested whether phytochemical differences between closely related plant species are correlated with specialist host choice. We conducted no-choice feeding trials using 17 plant species of three genera of tribe Senecioneae (Jacobaea, Packera, and Senecio; Asteraceae) and a more distantly related species (Cynoglossum officinale; Boraginaceae) containing pyrrolizidine alkaloids (PAs), and four PA-sequestering specialist herbivores of the genus Longitarsus (Chrysomelidae). We also assessed whether variation in feeding by specialist herbivores is attributable to different resource use strategies of the tested plant species. Plant resource use strategy was quantified by measuring leaf dry matter content, which is related to both plant nutritive value and to plant investment in quantitative defences. We found no evidence that intra-generic differences in PA profiles affect feeding by specialist herbivores. Instead, our results indicate that decisions to begin feeding are related to plant resource use strategy, while decisions to continue feeding are not based on any plant characteristics measured in this study. These findings imply that PA composition does not significantly affect host choice by these specialist herbivores. Leaf dry matter content is somewhat phylogenetically conserved, indicating that plants may have difficulty altering resource use strategy in response to selection pressure by herbivores and other environmental factors on an evolutionary time scale.     

Do arbuscular mycorrhizal fungi affect the allometric partition of host plant biomass to shoots and roots? A meta-analysis of studies from 1990 to 2010

Arbuscular mycorrhizas (AM) are ubiquitous root symbioses with often pervasive effects on the plant host, one of which may be above- and belowground biomass allocation. A meta-analysis was conducted on 516 trials that were described in 90 available articles to examine whether AM colonization could result in a modification of partitioning of plant biomass in shoots and roots. It was hypothesized that alleviating plant nutrient limitations could result in a decrease of root to shoot (R/S) ratio in AM plants or, alternatively, the direction of shifts in the R/S ratio would be determined by the changes in total dry biomass. In our analysis, we considered four types of stresses: drought stress, single heavy metal stress, multiple heavy metal stress, and other potential abiotic plant stress factors. When disregarding any factors that could regulate effects, including stress status and mode of propagation, the overall AM effect was a significant modification of biomass towards shoot growth. However, the responses of stressed and clonally propagated plants differed from those of seed-grown unstressed plants. Our meta-analysis detected a considerable decline in the R/S ratio when plants were grown from seeds in the absence of abiotic stresses. Moreover, we demonstrate that additional regulators of the AM-mediated impact on R/S ratio were presence of competition from other plants, plant growth outcome of the symbiosis, growth substrate volume, experimental duration, and the identities of both plant and AM fungus. Our results indicate that a prediction of AM effects on R/S allocation becomes more accurate when considering regulators, most notably propagation mode and stress. We discuss possible mechanisms through which stress and other regulators may operate.     

Can aphid-induced plant signals be transmitted aerially and through the rhizosphere?

Aphids, through their close association with plants, cause systemic release of semiochemicals. These may have negative effects on subsequent aphid colonisation and can also have positive roles with insects that are antagonistic to aphid development, for example parasitoids. One of the semiochemicals involved in host selection by aphids is methyl salicylate, and since this compound was shown to have a role as a plant stress signal, the hypothesis that aphids might facilitate identification of new plant signals was examined. Confirmation was obtained during an investigation of avoidance of unsuitable hosts by the lettuce aphid, Nasonovia ribis-nigri. (Z)-Jasmone was identified as a plant-derived semiochemical acting negatively for a number of aphid species, and positively for insect antagonists such as parasitoids and predators. However, when the compound was employed at 0.1 ppm in air above intact plants, these plants then attracted aphid parasitoids long after the (Z)-jasmone itself was no longer detectable. A specific interaction was proposed, since the (Z)-jasmone appeared to be selectively taken up by the plants. Aerial interactions between intact barley plants from different cultivars, which may be differentially releasing stress associated signals, can also influence acceptability to aphids. Furthermore, it has been shown that exudates from the roots of aphid-infested plants, grown hydroponically or in soil, cause intact plants to become more attractive to parasitoids.     

Can the scaling of plant nitrogen to phosphorus be altered by global change? An empirical test

全球变化可能引起土壤中各种养分的供应失衡,进而导致陆地植物中氮(N)和磷(P)元素化学计量学的不平衡。前人的研究报道了全球变化因子对植物N、P含量和N:P的影响,但鲜有研究探讨全球变化因子是否影响以及如何影响这两种元素之间的异速关系。本研究利用改变降水(增雨和干旱)、增温和N添加处理的野外控制试验,结合异速函数 N = βP^α (或对数转换后的线性关系：Log N = Log β + α Log P),检验了中国西北地区黄土高原半干旱草原植物N和P化学计量特征及N和P之间的异速关系对这些全球变化因子的响应。研究结果表明,干旱和增温均降低了植物P浓度,N添加增加了植物N浓度,这些都导致植物N:P增加。干旱、增温和N添加没有显著改变植物N和P浓度之间异速关系的斜率(即N和P浓度对数转换后的线性关系斜率α),但是显著增加了其截距(Log β)。这些结果表明,全球变化因子可能不会影响植物N和P之间的协同变化关系,植物中N和P之间可能存在着紧密的耦合关系。这些结果将有助于我们更好地理解全球变化背景下的植物养分动态和元素平衡。     

Gene expression in mycorrhizal orchid protocorms suggests a friendly plant–fungus relationship

Main conclusion

Orchid mycorrhiza has been often interpreted as an antagonistic relationship. Our data on mycorrhizal protocorms do not support this view as plant defence genes were not induced, whereas some nodulin-like genes were significantly up-regulated. Orchids fully depend on symbiotic interactions with specific soil fungi for seed germination and early development. Germinated seeds give rise to a protocorm, a heterotrophic organ that acquires nutrients, including organic carbon, from the mycorrhizal partner. It has long been debated if this interaction is mutualistic or antagonistic. To investigate the molecular bases of the orchid response to mycorrhizal invasion, we developed a symbiotic in vitro system between Serapias vomeracea, a Mediterranean green meadow orchid, and the rhizoctonia-like fungus Tulasnella calospora. 454 pyrosequencing was used to generate an inventory of plant and fungal genes expressed in mycorrhizal protocorms, and plant genes could be reliably identified with a customized bioinformatic pipeline. A small panel of plant genes was selected and expression was assessed by real-time quantitative PCR in mycorrhizal and non-mycorrhizal protocorm tissues. Among these genes were some markers of mutualistic (e.g. nodulins) as well as antagonistic (e.g. pathogenesis-related and wound/stress-induced) genes. None of the pathogenesis or wound/stress-related genes were significantly up-regulated in mycorrhizal tissues, suggesting that fungal colonization does not trigger strong plant defence responses. In addition, the highest expression fold change in mycorrhizal tissues was found for a nodulin-like gene similar to the plastocyanin domain-containing ENOD55. Another nodulin-like gene significantly more expressed in the symbiotic tissues of mycorrhizal protocorms was similar to a sugar transporter of the SWEET family. Two genes coding for mannose-binding lectins were significantly up-regulated in the presence of the mycorrhizal fungus, but their role in the symbiosis is unclear.     

Do arbuscular mycorrhizal fungi recolonize revegetated grasslands?

Fifteen native and common exotic herbaceous species from four functional groups (C4 grass, C3 grass, chamaephyte and hemicryptophyte) occurring within remnant and revegetated grassland and grassy woodlands were sampled for evidence of structures associated with functioning arbuscular mycorrhizal fungi (AMF) from across a broad geographical range of central and south‐western Victoria, Australia. Revegetated communities had been established on ex‐agricultural land by direct seeding. They included sites that had been kept fallow with herbicide for up to 3 years prior to seeding and those from which topsoil had been removed (scalped) to a depth of 100 mm prior to seeding. Structures associated with AMF (external and internal aseptate hyphae, arbuscules and vesicles) were observed in root samples from all native and exotic species, regardless of site history (remnant or revegetated; fallowed or scalped). These findings indicate that AMF are ubiquitous in the herbaceous flora of this region (native and exotic), even in situations where sites had been intensively disturbed prior to revegetation treatment. However, while there was evidence of AMF in all revegetated communities, only sites which had been scalped prior to direct seeding supported species‐rich native herbaceous communities.     

Are there benefits of simultaneous root colonization by different arbuscular mycorrhizal fungi?

Arbuscular mycorrhizal fungal (AMF) communities were established in pots using fungal isolates from a single field in Switzerland. It was tested whether multispecies mixtures provided more phosphorus and supported greater plant growth than single AMF species. Two host plants, medic (Medicago truncatula) and leek (Allium porrum), were inoculated with three AMF species (Glomus mosseae, G. claroideum and G. intraradices), either separately or in mixtures. The composition of the AMF communities in the roots was assessed using real-time PCR to determine the copy number of large ribosomal subunit genes. Fungal communities in the roots were usually dominated by one AMF species (G. mosseae). The composition of the communities depended on both plant identity and the time of harvest. Leek colonized by a mixture of G. claroideum and G. intraradices acquired more P than with either of the two AMF separately. Direct evidence is provided for functional complementarity among species within the AMF community colonizing a single root system. Competition among the species poses a major challenge in interpreting experiments with mixed inoculations, but this is greatly facilitated by use of real-time PCR.     

Can the IUCN criteria be effectively applied to peripheral isolated plant populations?

The IUCN criteria 2001 are considered one of the best methods to evaluate species extinction risk at the global and regional levels. The aim of this work is to test the applicability of the IUCN criteria to peripheral isolated plant populations (PIPPs). PIPPs have been a topic of scientific debate in Conservation Biology for about 15 years and international conventions such as ESPC address the issue of their conservation. Conservation measures often rely on Red Lists based on IUCN criteria, but there is little evidence supporting their application to PIPPs. In this work, we tested the hypothesis that PIPPs’ intrinsic restricted range and rarity lead to the overestimation of their extinction risk. We compared and analyzed four IUCN criteria (A, B, C, D), considering 17 species with PIPPs in different Italian administrative regions. Special attention must be given to the spatial scale at which PIPPs are assessed, the evaluation of the threats affecting the populations, and their decline. PIPPs should not be assessed within political boundaries and we propose a new area designation that better corresponds to the characteristics of PIPPs. Criterion B is strongly biased by restricted range and overestimates the extinction risk of PIPPs, particularly when the population decline is only suspected and not observed. In this case, criterion D more accurately assesses the status of PIPPs. Criterion A is also suitable for assessing PIPPs, because it is not affected by their phytogeographic rarity. The proposed statements could also be valid for the global assessment of narrow endemic species.     

Do arbuscular mycorrhizal fungi play a role in the ability of rare plant species to colonize abandoned fields?

While some plant species colonize abandoned agricultural fields and dry grasslands with similar frequency (generalists), others are absent or underrepresented in abandoned fields (specialists). We tested if inoculation with dry grassland or abandoned field soil could improve specialist performance in an abandoned field and compared the effects of inoculation in the stage of sown seeds and transplanted seedlings. Arbuscular mycorrhizal fungi from abandoned field had higher root colonization potential. This could explain the higher performance of the sown specialists inoculated with the abandoned field inoculum compared to those inoculated with dry grassland inoculum. This difference disappeared when specialists were transplanted instead of sown. The results do not provide any support for higher performance of specialists inoculated with dry grassland inoculum. Transplantation, however, seems to be an efficient way to introduce specialists into the abandoned fields.     

Is plant performance limited by abundance of arbuscular mycorrhizal fungi? A meta-analysis of studies published between 1988 and 2003

We conducted meta-analyses of 290 published field and glasshouse trials to determine the effects of various agricultural practices on mycorrhizal colonization in nonsterile soils, and the consequence of those effects on yield, biomass, and phosphorus (P) concentration. Mycorrhizal colonization was increased most by inoculation (29% increase), followed by shortened fallow (20%) and reduced soil disturbance (7%). The effect of crop rotation depended on whether the crop was mycorrhizal. Increased colonization resulted in a yield increase in the field of 23% across all management practices. Biomass at harvest and shoot P concentration in early season were increased by inoculation (57 and 33%, respectively) and shortened fallow (55 and 24%). Reduced disturbance increased shoot P concentration by 27%, but biomass was not significantly affected. Biomass was significantly reduced in 2% of all trials in which there was a significant increase in colonization. Irrespective of management practice, an increased mycorrhizal colonization was less likely to increase biomass if either soil P or indigenous inoculum potential was high.