Mycelium of Arbuscular Mycorrhizal fungi (AMF) from different genera: form, function and detection

By J. C. Dodd, C. Boddington, Alia Rodriguez, C. González-Chávez, I. Mansur. Plant and Soil, 2000

241 citations recorded by the source corpus.

Subfields: Molecular Biology, Pharmacology, Plant Science

View Paper: https://www.semanticscholar.org/paper/393fcafad89993126d79422d00c82a5deff16ec5

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Citations in the corpus

Methods of studying soil microbial diversity. (2004, background): “Therefore, the single-sequence, single-species hypothesis may not fit with AMF and diversity could be overestimated (Dodd et al., 2000; Schubler et al., 2001).”
Networks of power and influence: the role of mycorrhizal mycelium in controlling plant communities and agroecosystem functioning (2004, background): “The centre of the core is within 1 cm of the nearest roots outside, and at this distance Jakobsen et al. (1992a) found that for isolates of Acaulospora, Scutellospora, and Glomus the concentration of AM hyphal length per gram of soil was 60%–110% of values found at the root surface.”
Diversity of arbuscular mycorrhizal fungi in the roots of perennial plants and their effect on plant performance (2004, background): “Sporulation of some AM fungi, especially those from the genera Scutellospora and Gigaspora, needs to be preceded by a prolonged phase of root colonisation (Dodd et al. 2000).”
Mycorrhiza : state of the art, genetics and molecular biology, eco-function, biotechnology, eco-physiology, structure and systematics (2008, background): “Another benefit to the plant of interest is that photosynthates are needed only for maintenance of the AM fungi following colonization, and not for the development of the extraradical mycelium since it was preestablished (Dodd et al. 2000).”
Mycorrhizal responses to nitrogen fertilization in boreal ecosystems: potential consequences for soil carbon storage (2007, background): “Another possibility includes a shift in the AM community toward Glomus species, which tend to produce more intraradical structures and less external hyphae than do other AM species (Klironomos et al., 1998; Dodd et al., 2000; van Aarle et al., 2002; Treseder, 2005).”
Role of niche restrictions and dispersal in the composition of arbuscular mycorrhizal fungal communities (2007, background): “Possibly, differential biomass allocation and growth patterns of the external hyphae between Gigasporaceae and Glomeraceae, as detected by Hart & Reader (2002) and Dodd et al. (2000), are affected by texture.”
Impact of tillage system on arbuscular mycorrhiza fungal communities in the soil under Mediterranean conditions (2012, background): “are believed to survive perturbations well and hence prevail in highly disturbed agricultural systems (Douds et al., 1995; Dodd et al., 2000).”
Mycorrhizal dynamics under elevated CO2 and nitrogen fertilization in a warm temperate forest (2008, background): “Glomus tends to produce fewer external hyphae per unit root length colonized (Klironomos et al. 1998; Dodd et al. 2000).”
Arbuscular mycorrhizal fungi as mediators of ecosystem responses to nitrogen deposition: A trait‐based predictive framework (2018, background): “In other words, Glomeraceae tend to be associated with higher soil N availability than the Gigasporaceae.”
The impact of chlorothalonil application on soil bacterial and fungal populations as assessed by denaturing gradient gel electrophoresis (2002, background): “and Chaetomium spp., both common terrestrial fungi genera ( Dodd et al., 2000 ), and Fusarium spp., members of which are known maize pathogens (Soonthornpoct et al., 2000).”