Specificity and resilience in the arbuscular mycorrhizal fungi of a natural woodland community

By T. Helgason, J. Merryweather, J. Young, A. Fitter. 2007

166 citations recorded by the source corpus.

Subfields: Insect Science, Nature and Landscape Conservation, Plant Science

View Paper: https://www.semanticscholar.org/paper/534e69b8cc7dd687fb7f32fac2509dfd5170118a

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Citations in the corpus

Nitrogen deposition and precipitation induced phylogenetic clustering of arbuscular mycorrhizal fungal communities (2017, background): “, 2015), and subsequently shape AMF communities (Vandenkoornhuyse et al., 2003; Helgason et al., 2007; Veresoglou and Rillig, 2014).”
Field inoculation effectiveness of native and exotic arbuscular mycorrhizal fungi in a Mediterranean agricultural soil (2011, background): “alexandrinum, suggesting a differential compatibility between native and exotic AM fungal isolates and host plants (Klironomos, 2003; Helgason et al., 2007).”
Six-year fertilization modifies the biodiversity of arbuscular mycorrhizal fungi in a temperate steppe in Inner Mongolia (2014, background): “With regard to AMF species distribution, several studies showed thatR. intraradiceshadawide distribution in various environments (Öpik et al., 2006) and host species (Helgason et al., 2007).”
The unseen majority: soil microbes as drivers of plant diversity and productivity in terrestrial ecosystems. (2008, background): “A recent study indicated that these generalist and easily cultured AM fungi are also more resistant to soil perturbation, while specialist AM fungi (several of them still uncultured) declined (Helgason et al. 2007).”
Shrubs influence arbuscular mycorrhizal fungi communities in a semi-arid environment (2011, background): “The use of molecular techniques revealed an unexpectedly high diversity of AMF (Helgason et al., 2002; Redecker, 2002) and strong host specificity (Helgason et al., 2007; Johnson et al., 2003; Vandenkoornhuyse et al., 2002) challenging the traditional view of * Corresponding author.”
The application of an organic amendment modifies the arbuscular mycorrhizal fungal communities colonizing native seedlings grown in a heavy-metal-polluted soil (2011, background): “intraradices can be considered the generalist fungal species “par excellence” since it is present in all the places around the world investigated so far (Öpik et al., 2006; Helgason et al., 2007).”
The online database MaarjAM reveals global and ecosystemic distribution patterns in arbuscular mycorrhizal fungi (Glomeromycota). (2010, background): “Indeed, metadata linked to sequence datasets of Glomeromycota has already provided insights into AM fungal community composition among ecosystems (Öpik et al., 2006), and in relation to host range (Helgason et al., 2007) and dominance patterns (Dumbrell et al., 2010).”
Plant type differently promote the arbuscular mycorrhizal fungi biodiversity in the rhizosphere after revegetation of a degraded, semiarid land (2010, background): “intraradices is considered the most-common taxon detected in many host species (Helgason et al., 2007) and ecosystems (Öpik et al.”
Root-colonizing and soil-borne communities of arbuscular mycorrhizal fungi in a temperate forest understorey1 (2014, background): “Given that the number of recorded AMF taxa at a site is typically an order ofmagnitude lower than that of associated plant species, and that most (cultured) AMF can colonize most plant species, AMF have not been considered to be host-specific (Helgason et al. 2007; Smith and Read 2008).”
Relative roles of niche and neutral processes in structuring a soil microbial community (2010, background): “However, previous studies on soils with a smaller range of pH have suggested that host plant species is an important factor structuring AM fungal communities (Helgason et al., 2007).”
Community structure of arbuscular mycorrhizal fungi associated with Robinia pseudoacacia in uncontaminated and heavy metal contaminated soils (2015, unknown): “, 2003) and host species (Helgason et al., 2007).”