Composition of root‐colonizing arbuscular mycorrhizal fungal communities in different ecosystems around the globe

By M. Öpik, M. Moora, J. Liira, M. Zobel. 2006

583 citations recorded by the source corpus.

Subfields: Insect Science, Pharmacology, Plant Science

View Paper: https://www.semanticscholar.org/paper/73db95d3ff806f90ef9f3716979d38463a08f0e7

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Citations in the corpus

A general suite of fungal endophytes dominate the roots of two dominant grasses in a semiarid grassland (2010, background): “Additional and related work from several laboratories (including ours) have suggested that plant species harbor a general (rather than specific) suite of root associated fungal communities (Opik et al., 2003, 2006; Higgins et al., 2007; Porras-Alfaro et al., 2007).”
Idiosyncrasy and overdominance in the structure of natural communities of arbuscular mycorrhizal fungi: is there a role for stochastic processes? (2010, methodology): “4; Opik et al. 2006).”
Agricultural intensification reduces microbial network complexity and the abundance of keystone taxa in roots (2018, methodology): “groups, including arbuscular mycorrhizal fungi (AMF) using traditional techniques [27, 28].”
Global diversity and distribution of arbuscular mycorrhizal fungi (2011, unknown): “Molecular surveys of AM fungi at the regional scale or larger are uncommon and have thus-far been restricted to only one gene (18S) in the most abundant taxa (Dumbrell et al., 2010; Öpik et al., 2006, 2010).”
Global change and species interactions in terrestrial ecosystems. (2008, background): “Effects of GEC on plant–fungal mutualisms are more variable, but mycorrhizal community composition is often altered by land use intensification or biological invasion (Mummey & Rillig 2006; Opik et al. 2006).”
Effect of long-term nitrogen fertilization on mycorrhizal fungi associated with a dominant grass in a semiarid grassland (2007, methodology): “Our results are in agreement with other studies in which some AMF show global distribution, single species dominance, and low host specificity (Öpik et al. 2006; Santos et al. 2006; Stukenbrock and Rosendahl 2005).”
Plant defence theory re‐examined: nonlinear expectations based on the costs and benefits of resource mutualisms (2011, background): “plants are associated with multiple species of fungi (Opik et al. 2006), which may access a greater range of nutrients than a single fungal species (Koide 2000; Jansa, Smith & Smith 2008).”
Specificity and resilience in the arbuscular mycorrhizal fungi of a natural woodland community (2007, background): “…(e.g. Sanders & Fitter 1992; Clapp et al. 1995; Bever et al. 1996; Eom et al. 2000; Helgason et al. 2002; Husband et al. 2002; Öpik et al. 2003; Vandenkoornhuyse et al. 2003; Johnson et al. 2004; Öpik et al. 2006), but none of these have shown whether this pattern is caused by host specificity.”
Variation in forest soil fungal diversity along a latitudinal gradient (2013, background): “…in contrast to bacterial studies, surveys of soil fungal diversity and composition across large geographic scales remain rare (Green et al. 2004; Öpik et al. 2006) even though molecular techniques now offer a unique possibility and potential to study large scale biogeographical patterns (Fierer…”
Plant diversity predicts beta but not alpha diversity of soil microbes across grasslands worldwide. (2015, methodology): “We focused on grasslands as widely used model systems for investigating aboveground – belowground relationships (Eisenhauer et al. 2011); and because there is already evidence that major biomes harbour distinct below-ground communities (Fierer & Jackson 2006; € Opik et al. 2006; Fierer et al. 2012).”
Socialism in soil? The importance of mycorrhizal fungal networks for facilitation in natural ecosystems (2009, background): “This lack of specificity is also reflected by the fact that someAM fungal species have aworldwide distribution, associating with a wide range of plant species in very different ecosystems (Opik et al. 2006).”
Plant type differently promote the arbuscular mycorrhizal fungi biodiversity in the rhizosphere after revegetation of a degraded, semiarid land (2010, unknown): “, 2007) and ecosystems (Öpik et al., 2006).”
Global patterns of plant root colonization intensity by mycorrhizal fungi explained by climate and soil chemistry (2015, background): “extrapolated to a global scale, because community compositions of vascular plants and mycorrhizal fungi vary greatly across the globe (Opik et al., 2006; Kivlin et al., 2011; Tedersoo et al., 2012) while they both influence the functioning of mycorrhizal symbiosis (Ji et al.”