» Articles » PMID: 23392533

Seasonal Dynamics of Boletus Edulis and Lactarius Deliciosus Extraradical Mycelium in Pine Forests of Central Spain

Overview
Journal Mycorrhiza
Date 2013 Feb 9
PMID 23392533
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

The annual belowground dynamics of extraradical soil mycelium and sporocarp production of two ectomycorrhizal fungi, Boletus edulis and Lactarius deliciosus, have been studied in two different pine forests (Pinar Grande and Pinares Llanos, respectively) in Soria (central Spain). Soil samples (five per plot) were taken monthly (from September 2009 to August 2010 in Pinar Grande and from September 2010 to September 2011 in Pinares Llanos) in eight permanent plots (four for each site). B. edulis and L. deliciosus extraradical soil mycelium was quantified by real-time polymerase chain reaction, with DNA extracted from soil samples, using specific primers and TaqMan® probes. The quantities of B. edulis soil mycelium did not differ significantly between plots, but there was a significant difference over time with a maximum in February (0.1576 mg mycelium/g soil) and a minimum in October (0.0170 mg mycelium/g soil). For L. deliciosus, significant differences were detected between plots and over time. The highest amount of mycelium was found in December (1.84 mg mycelium/g soil) and the minimum in February (0.0332 mg mycelium/g soil). B. edulis mycelium quantities were positively correlated with precipitation of the current month and negatively correlated with the mean temperature of the previous month. Mycelium biomass of L. deliciosus was positively correlated with relative humidity and negatively correlated with mean temperature and radiation. No significant correlation between productivity of the plots with the soil mycelium biomass was observed for any of the two species. No correlations were found between B. edulis sporocarp production and weather parameters. Sporocarp production of L. deliciosus was positively correlated with precipitation and relative humidity and negatively correlated with maximum and minimum temperatures. Both species have similar distribution over time, presenting an annual dynamics characterized by a seasonal variability, with a clear increase on the amounts of biomass during the coldest months of the year. Soil mycelial dynamics of both species are strongly dependent on the weather.

Citing Articles

Cultivation studies of edible ectomycorrhizal mushrooms: successful establishment of ectomycorrhizal associations and efficient production of fruiting bodies.

Yamada A Mycoscience. 2023; 63(6):235-246.

PMID: 37089523 PMC: 10043572. DOI: 10.47371/mycosci.2022.08.004.


Design and Validation of qPCR-Specific Primers for Quantification of the Marketed and in Soil.

Arenas F, Morte A, Navarro-Rodenas A J Fungi (Basel). 2022; 8(10).

PMID: 36294660 PMC: 9605127. DOI: 10.3390/jof8101095.


Effects of rhizosphere fungi on the chemical composition of fruits of the medicinal plant Cinnamomum migao endemic to southwestern China.

Chen J, Huang X, Tong B, Wang D, Liu J, Liao X BMC Microbiol. 2021; 21(1):206.

PMID: 34229615 PMC: 8259389. DOI: 10.1186/s12866-021-02216-z.


High resilience of the mycorrhizal community to prescribed seasonal burnings in eastern Mediterranean woodlands.

Livne-Luzon S, Shemesh H, Osem Y, Carmel Y, Migael H, Avidan Y Mycorrhiza. 2021; 31(2):203-216.

PMID: 33475801 DOI: 10.1007/s00572-020-01010-5.


Production of Fungal Mycelia in a Temperate Coniferous Forest Shows Distinct Seasonal Patterns.

Stursova M, Kohout P, Human Z, Baldrian P J Fungi (Basel). 2020; 6(4).

PMID: 32993121 PMC: 7712845. DOI: 10.3390/jof6040190.


References
1.
Parlade J, De la Varga H, De Miguel A, Saez R, Pera J . Quantification of extraradical mycelium of Tuber melanosporum in soils from truffle orchards in northern Spain. Mycorrhiza. 2012; 23(2):99-106. DOI: 10.1007/s00572-012-0454-y. View

2.
Schubert R, Raidl S, Funk R, Bahnweg G, Muller-Starck G, Agerer R . Quantitative detection of agar-cultivated and rhizotron-grown Piloderma croceum Erikss. & Hjortst. by ITS1-based fluorescent PCR. Mycorrhiza. 2003; 13(3):159-65. DOI: 10.1007/s00572-002-0212-7. View

3.
Hagerberg D, Wallander H . The impact of forest residue removal and wood ash amendment on the growth of the ectomycorrhizal external mycelium. FEMS Microbiol Ecol. 2009; 39(2):139-46. DOI: 10.1111/j.1574-6941.2002.tb00915.x. View

4.
Kjoller R . Disproportionate abundance between ectomycorrhizal root tips and their associated mycelia. FEMS Microbiol Ecol. 2006; 58(2):214-24. DOI: 10.1111/j.1574-6941.2006.00166.x. View

5.
Ortega-Martinez P, Agueda B, Fernandez-Toiran L, Martinez-Pena F . Tree age influences on the development of edible ectomycorrhizal fungi sporocarps in Pinus sylvestris stands. Mycorrhiza. 2010; 21(1):65-70. DOI: 10.1007/s00572-010-0320-8. View