Extensive knowledge of various ectomycorrhizal fungal communities has been obtained over the past 10 years based on molecular identification of the fungi colonizing fine roots. In contrast, only limited information exists about the species composition of ectomycorrhizal hyphae in soil. This study compared the ectomycorrhizal external mycelial community with the adjacent root-tip community in a ...

Plants interact with a diversity of microorganisms, and there is often concordance in their community structures. Because most community-level studies are observational, it is unclear if such concordance arises because of host specificity, in which microorganisms or plants limit each other's occurrence. Using a reciprocal transplant experiment, we tested the hypothesis that host specificity bet...

Currently in Western Australia, phosphite is being used to contain the root and collar rot pathogen, Phytophthora cinnamomi, in native plant communities. There have been reports of negative effects of phosphite on arbuscular mycorrhiza (AM), so there are concerns that it may have a deleterious effect on other mycorrhizal fungi. Two glasshouse experiments were undertaken to determine the impact ...

The vast forests of the Pacific Northwest region of the United States, an area outlined by the states of Oregon, Washington, and Idaho, are well known for their rich diversity of macrofungi. The forests are dominated by trees in the Pinaceae with about 20 species in the genera Abies, Larix, Picea, Pinus, Pseudotsuga, and Tsuga. All form ectomycorrhizas with fungi in the Basidiomycota, Ascomycot...

Ectomycorrhizal fungi (ECMF) are an important biotic factor in the survival of conifer seedlings under stressful conditions and therefore have the potential to facilitate conifer establishment into alpine and tundra habitats. In order to assess patterns of ectomycorrhizal availability and community structure above treeline, we conducted soil bioassays in which Picea mariana (black spruce) seedl...

Soils in boreal forests contain large stocks of carbon. Plants are the main source of this carbon through tissue residues and root exudates. A major part of the exudates are allocated to symbiotic ectomycorrhizal fungi. In return, the plant receives nutrients, in particular nitrogen from the mycorrhizal fungi. To capture the nitrogen, the fungi must at least partly disrupt the recalcitrant orga...

Pinus densiflora seedlings were inoculated with three indigenous ectomycorrhizal fungi (Cenococcum geophilum, Rhizopogon roseolus and Russula densifolia) in single-, two-, and three-species treatments. After 8 months, the colonization rates of each ectomycorrhizal species, seedling growth and the nutrition were assessed in each treatment. P. densiflora seedlings inoculated with different ECM sp...

The amount of carbon plants allocate to mycorrhizal symbionts exceeds that emitted by human activity annually. Senescent ectomycorrhizal roots represent a large input of carbon into soils, but their fate remains unknown. Here, we present the surprising result that, despite much higher nitrogen concentrations, roots colonized by ectomycorrhizal (EM) fungi lost only one-third as much carbon as no...

In order to assess changes in the community structure of ectomycorrhizal fungi across the tree line, data on distributions of fungi and their host plants, as well as on edaphic factors and stand age, were collected at two montane sites in the Front Range of the Canadian Rockies. Canonical correspondence analysis (CCA) was used to explore relationships between fungal species composition and envi...

Access to deeper soil water and water-conserving traits should reduce water stress for ectomycorrhizal fungi, permitting function during drought. Here, we explored whether epigeous fruiting of ectomycorrhizal fungi during drought was facilitated by access to deep soil water, how much water was lost from sporocarps, and how sporocarp surface to volume ratios affected water-loss rates. We used ox...