scholarly journals Species richness and nitrogen supply regulate the productivity and respiration of ectomycorrhizal fungi in pure culture

2012 ◽  
Vol 5 (2) ◽  
pp. 211-222 ◽  
Author(s):  
Anna Wilkinson ◽  
Martin Solan ◽  
Ian Alexander ◽  
David Johnson
2020 ◽  
Author(s):  
Akotchayé Sylvestre Badou ◽  
Roel D. Houdanon ◽  
Kassim I. Tchan ◽  
D.M.T. Apollon Hègbè ◽  
Nourou Soulemane Yorou

Abstract Background: The ectomycorrhizal fungi display strong fluctuations during the mycological season. However, how abiotic parameters affect the fruiting sequences of ectomycorrhizal fungi and also the direction and extent of this effect are not yet tapped adequately. The present study seeks to assess the microclimate effect on the natural production of boletes. Nine permanent plots of 2500 m2 (50m x 50m) split into 25 subplots of 100 m2 (10m x 10m) were installed in three different vegetation dominated respectively by Isoberlinia doka, Isoberlinia tomentosa and Uapaca togoensis. Microclimatic parameters were recorded each 30 minutes throughout by mean of a Micro Station Data Logger - H21-002 the mycological seasons. Each plot was surveyed twice a week (from May to October) over three years (2015, 2016 and 2017) to record the presence/absence of fruit bodies and fresh biomass of boletes. To evaluate the effect of time and microclimate variables on natural production, we used mixed effects and generalized linear models using R version 3.5.3. Results: In total, during the three years (2015, 2016 and 2017), we recorded 14 species of boletes. Species richness does not change over time (P > 0.05). In addition, fresh biomass varies within years and vegetation (P < 0.05). The combination of year and month of collection has a significant effect on the number of fruit bodies (P < 0.05). Only the soil moisture has a significant positive influence on the species richness of boletes (P > 0.05). Conclusions: When the soil moisture decreases by four units, the number of fruit bodies of ectomycorrhizal fungi is significantly reduced by one unit. Therefore, above 0.25 m3 / m3 and below 0.05 m3 / m3 there is a decrease in the number of fruit bodies.


2000 ◽  
Vol 77 (12) ◽  
pp. 1699-1711 ◽  
Author(s):  
Thomas E O'Dell ◽  
Joseph F Ammirati ◽  
Edward G Schreiner

Sporocarps of epigeous ectomycorrhizal fungi and vegetation data were collected from eight Tsuga heterophylla (Raf.) Sarg. - Pseudotsuga menziesii (Mirb.) Franco stands along a wet to dry gradient in Olympic National Park, Washington, U.S.A. One hundred and fifty species of ectomycorrhizal fungi were collected from a total sample area of 2.08 ha. Over 2 years, fungal species richness ranged from 19 to 67 taxa per stand. Sporocarp standing crop ranged from 0 to 3.8 kg/ha, averaging 0.58 kg/ha, 0.06 kg/ha in spring and 0.97 kg/ha in fall. Sporocarp standing crop and fungal species richness were correlated with precipitation. These results demonstrated that ectomycorrhizal fungal sporocarp abundance and species richness can be partly explained in terms of an environmental gradient.


2013 ◽  
Vol 42 (1) ◽  
pp. 59-68
Author(s):  
Danutė Stankovičienė ◽  
Jonas Kaspravičius

The diversity of ectomycorrhizal fungi and sporocarps abundance were investigated in 2003-2005 at nine permanent study plots in a 50-year-old pine forest. Diversity of ectomycorrhizal fungi consisted of 53 taxa and the majority of them belonged to the genera <em>Cortinarius, Russula, Amanita</em> and <em>Tricholoma</em>. The most frequent species, whose fruit bodies were found in each study plot, were <em>C. cibarius, L. necator L. rufus, P. involutus, R. aeruginea, T. saponaceum</em> and the most abundant species which made the main part of total sporocarp yield were <em>C. cibarius</em> and <em>P. involutus</em>. The lowest species richness of ectomycorrhizal fungi was in study plots with the densest cover of grasses. Maximum of species over the fruiting period was characteristic for October and for September. It was noticed that some species virtually never occurred together at the same plot (eg. <em>C. cibarius</em> and <em>H. aurantiaca</em>), meanwhile others occurred together quite frequently (eg. <em>H.aurantiaca</em> and <em>X. badius</em>).


2010 ◽  
Vol 187 (2) ◽  
pp. 485-493 ◽  
Author(s):  
Mona N. Högberg ◽  
Maria J. I. Briones ◽  
Sonja G. Keel ◽  
Daniel B. Metcalfe ◽  
Catherine Campbell ◽  
...  

1981 ◽  
Vol 59 (12) ◽  
pp. 2458-2465 ◽  
Author(s):  
R. K. Antibus ◽  
J. G. Croxdale ◽  
O. K. Miller ◽  
A. E. Linkins

Pure culture isolates were obtained from fungi fruiting in the vicinity of dwarf willows at Barrow and Cape Simpson, Alaska. Four of these isolates and one isolate from Maryland were tested for their ability to form ectomycorrhizae with cuttings of Salix rotundifolia under controlled environmental conditions. Isolates of Entoloma sericeum, Hebelomapusillum, and Cenococcum geophilum from Barrow and Cape Simpson, Alaska all formed typical ectomycorrhizae with S. rotundifolia, while an isolate of C. geophilum from a temperate ecosystem (Maryland) did not.All of the ectomycorrhizae synthesized with S. rotundifolia, plus uncolonized roots, demonstrated an ability to hydrolyze p-nitrophenyl phosphate at a pH of 4.7. The acid phosphatase activity of E. sericeum ectomycorrhizae was from 10 to 40 times as great as that demonstrated by other mycorrhizal and nonmycorrhizal roots on a surface area basis.


2021 ◽  
Vol 52 ◽  
pp. e1382
Author(s):  
Irma Díaz Aguilar ◽  
Magdalena Martínez-Reyes ◽  
Jesús Pérez-Moreno ◽  
Jorge Valdez-Carrasco

Background: The extraradical mycelium (ERM) of ectomycorrhizal fungi is a network inhabited by soil mesofauna, mainly collembolans and mites, forming interactions during the fungal life-cycle, from grazing on hyphae to spore dispersal. However, it is still unknown if ERM of ectomycorrhizal fungi could influence the structure of mesofauna assemblages. Objective: To evaluate the abundance and community composition of the mesofauna inhabiting the ERM of Hebeloma mesophaeum, Laccaria laccata and Wilcoxina sp. in Pinus greggii roots. Methods: Mesofauna was collected from the root balls of P. greggii with 80 % of colonization using a washing method. Results and conclusions: An effect was observed due to ERM differences on species richness and species dominance, but not an effect on the abundance and community composition of the mesofauna. However, Wilcoxina sp. presented the lowest species richness and diversity. Fungus-feeding collembolans shaped species-rich assemblages, being isotomid-tullbergid forms the soil-dwelling taxa. Entomobryidae and Hypogastruridae were the most common families on the soil surface, not being found in Wilcoxina sp., and only a few predatory mites of the Mesostigmata and Endeostigmata were found. The ectomycorrhizal mycelium constitutes a trophic niche of the mesofauna and it might be an evolutionary force in structuring species composition and diversity.


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