Species richness, abundance, and composition of hypogeous and epigeous ectomycorrhizal fungal sporocarps in young, rotation-age, and old-growth stands of Douglas-fir (Pseudotsuga menziesii) in the…

By Jane E. Smith, R. Molina, M. Huso, D. Luoma, D. McKay, M. Castellano, T. Lebel, Yana S. Valachovic. 2002

220 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Insect Science, Plant Science

View Paper: https://www.semanticscholar.org/paper/483e707bb0de2a0b99116ccec29a2995b40d8d9a

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology, Evolution, Behavior and Systematics

1. G. Kernaghan
2. J. Spatafora
3. M. Selosse
4. Yves Bergeron
5. B. Marçais
6. M. Gardes

In Insect Science

1. G. Kernaghan
2. R. Molina
3. Jane E. Smith
4. D. Luoma
5. J. Spatafora
6. A. B. Carey
7. Yves Bergeron
8. M. Buée

In Plant Science

1. G. Kernaghan
2. R. Molina
3. Jane E. Smith
4. D. Luoma
5. J. Spatafora
6. M. Selosse
7. Yves Bergeron
8. M. Buée

Citations in the corpus

• Biotic and abiotic factors affecting ectomycorrhizal diversity in boreal mixed-woods (2003, background): “Other factors that may affect ECM community structure include stand age (Visser 1995, Smith et al. 2002) and climate and topography (Claridge et al. 2000), but the dominant influences on ECM diversity in natural ecosystems have yet to be clearly identified.”
• Diversity and fruiting patterns of ectomycorrhizal and saprobic fungi in an old-growth Mediterranean forest dominated by Quercus ilex L. (2004, background): “For example, the genera Russula, Cortinarius, and Inocybe accounted for 49% of fruitbody collections and about 52% of taxonomic diversity in an oldgrowth stand of Douglas-fir (Smith et al. 2002).”
• Early impacts of forest restoration treatments on the ectomycorrhizal fungal community and fine root biomass in a mixed conifer forest (2005, background): “Piloderma and Russula species are typically abundant in mature and late-successional stands of temperate forests where large down wood in advanced stages of decay is common (Goodman & Trofymow 1998; Smith et al. 2000, 2002; Bergemann & Miller 2002).”
• Influence of tree species on richness and diversity of epigeous fungal communities in a French temperate forest stand (2011, background): “In theBreuil forest,we only found 49 epigeous EMF under Douglas-fir, whereas Smith et al. (2002), found 86 epigeous ectomycorrhizal species in a young (30e35 yr) Douglas-fir stand in Oregon.”
• Mycorrhizal diversity: Cause and effect? (2005, background): “EM diversity may also be related to stand age, as fungal species composition tends to change predictably over time (Last et al., 1987) and older conifer forests often support a greater number of fungal species than younger stands (Visser, 1995; Rao et al., 1997; Smith et al., 2002).”
• Biocomplexity and restoration of biodiversity in temperate coniferous forest: inducing spatial heterogeneity with variable‐density thinning (2003, background): “The long-term impacts of forest management on truffle production remain unclear, with inconsistent results from across the region (Carey et al., 2002; Smith et al., 2002).”
• Response of ectomycorrhizal fungus sporocarp production to varying levels and patterns of green-tree retention (2004, background): “Although we found total pre-treatment standing crops of mushrooms and truffles to be comparable (Table 2), Smith et al. (2002) found that truffle biomass exceeded mushroom biomass.”