Tolerance of arbuscular mycorrhizal fungi and microorganisms associated to their hyphosphere to aluminum in soil

Background: The elements that are toxic to arbuscular mycorrhizal fungi (AMF) and soil microorganisms, and the levels at which they affect them, are poorly known. Objective: To quantify the effects of: 1) aluminum added to the soil (0, 50 and 100 mg kg-1) and 2) inoculation with AMF (two isolates without prior exposure to aluminum, Acaulospora delicata and Gigaspora margarita, the native AMF community of a soil contaminated with Al, and a control without AMF) on the development of AMF mycelium and the hyphosphere-associated microbiota. Methods: A system with two compartments was used, a central compartment in which maize was sown and AMF were inoculated and a side compartment without root passage, where only the external mycelium was exposed to the different concentrations of Al. AMF external mycelium exposed to Al was quantified with the fatty-acid biomar-ker 16:1w5. Results and conclusions: Al concentrations up to 100 mg kg-1, controlling the pH of the soil, did not alter mycelium growth of any of the inoculated HMA either in the soil or in the roots. Aluminum added up to 100 mg kg-1 did not have a direct toxic effect on the growth of AMF mycelium and the hyphosphere-associated microbiota.

4. Fungal mutualisms

‘Fungal mutualisms’ considers symbiotic relationships in which the fungus and its partner benefit from their biological interaction. Examples of mutualisms with insects include fungi that trap scale insects, fungi cultivated by ambrosia beetles, and leaf-cutter ants and termites that grow mushroom gardens. These highly developed relationships involve substantial structural, biochemical, and behavioural adaptations in the fungi and insects. Fungi in mycorrhizal associations with plants operate as accessory root systems for plants, whereas fungi called endophytes house themselves inside plant tissues without any connection to an external mycelium. Lichens—composite organisms produced by a fungus and a single-celled alga or cyanobacterium—are the best-known mutualisms involving fungi.

Biomass of external mycelium of ectomycorrhizal fungi in Norway spruce stands in Poland

<p>Biomass of extramatrical mycorrhizal mycelium (EMM) was examined under canopies of mature Norway spruce trees grown in different forest stands in Poland. Two mountain forest sites (Brenna and Salmopol), one upland site (Zwierzyniec) and one lowland site (Mirachowo) have been investigated, using sand-filled mesh-bags method. The in-grow mesh-bags were buried in the soil for 12 months (since October up to the next October) or for 4 months (since June up to October) at four depths at each site: 5, 15, 30 and 45 cm (Brenna and Salmopol) or 60 cm (Zwierzyniec and Mirachowo). The mycelium biomass was estimated from the ergosterol content determined in the mesh-bags. The results indicated significant differences in EMM production and their vertical distribution between the mountain and the upland and lowland forest sites. The lowest EMM biomass was found at the experimental plot in the mountainious site Brenna. Considerable decrease of EMM biomass with the soil depth was recorded after 12 months of the mesh-bags incubation in soil in the upland and lowland sites, while in the mountain forests decrease of the EMM biomass in the lower soil depths diminished more gradually EMM biomass determined in the mesh-bags placed in soil at the upper 5 and 15 cm tended to be higher after 4 months than after 12 months of incubation period. Such results suggest that the time necessary for evaluation of EMM biomass in soil may be limited to the summer–autumn months, when the production of EMM is the highest. Variable stress factors can influence decreased ectomycorrhizal mycelium production and/or their destruction. Further research in different forest types and regions are needed for better understanding factors determining EMM biomass production and surviving in soil.</p>

Temperature stress in arbuscular mycorrhizal fungi: a test for adaptation to soil temperature in three isolates of Funneliformis mosseae from different climates

Climate change may impose stimulations or constraints on the mycorrhizal symbiosis by increasing and fluctuating temperatures. We conducted a study to compare the soil temperature response curves (6, 12, 18, and 24 oC) of three isolates of Funneliformis mosseae from different regions and climates (Finland, Denmark, Spain), to test if the isolates from cold environments were able to grow better at lower temperatures and the isolates from warmer environments grew better at higher temperatures. The results provided clear evidence suggesting no adaptation to soil temperature in these AMF isolates. All isolates showed reduced development and very little external mycelium growth at 6 and 12 oC, and similar increased development with increasing soil temperature. These results suggest that AMF have a narrow window to develop in cold regions where temperatures below 15 oC prevail.

Is cortical root colonization required for carbon transfer to arbuscular mycorrhizal fungi? Evidence from colonization phenotypes and spore production in the reduced mycorrhizal colonization (rmc) mutant of tomato

For the first time, the phenotypes formed in the reduced mycorrhizal colonization (rmc) Solanum lycopersicum L. (tomato) mutant with different arbuscular mycorrhizal (AM) fungi were used to explore the potential of different fungal structures to support development of external fungal mycelium and spores. The life cycle of AM fungi with rmc was followed for up to 24 weeks. Results showed that production of external mycelium was slight and transitory for those fungi that did not penetrate the roots of rmc (Pen–) ( Glomus intraradices DAOM181602 and Glomus etunicatum ). For fungi that penetrated the root epidermis and hypodermis (Coi–, Glomus coronatum and Scutellospora calospora ) the mycelium produced varied in size, but was always smaller than with the wild-type 76R. Spores were formed by these fungi with 76R but not with rmc. The only fungus forming a Myc+ phenotype with rmc, G. intraradices WFVAM23, produced as much mycelium with rmc as with 76R. We observed lipid accumulation in hyphae and vesicles in both plant genotypes with this fungus. Mature spores were formed with 76R. However, with rmc, spores remained small and (presumably) immature for up to 24 weeks. We conclude that significant carbon transfer from plant to fungus can occur in Coi– interactions with rmc in which no cortical colonization occurs. We speculate that both carbon transfer and root signals are required for mature spores to be produced.