Abstract

The fungal mycelium represents the essence of the fungal lifestyle, and understanding how a mycelium is constructed is of fundamental importance in fungal biology and ecology. Previous studies have examined initial developmental patterns or focused on a few strains, often mutants of model species, and frequently grown under non-harmonized growth conditions; these factors currently collectively hamper systematic insights into rules of mycelium architecture. To address this, we here use a broader suite of fungi (31 species including members of the Ascomycota, Basidiomycota and Mucoromycota), all isolated from the same soil, and tested for ten architectural traits under standardized laboratory conditions. We find great variability in traits among the saprobic fungal species, and detect several clear tradeoffs in mycelial architecture, for example between internodal length and hyphal diameter. Within the constraints so identified, we document otherwise great versatility in mycelium architecture in this set of fungi, and there was no evidence of trait ‘syndromes’ as might be expected. Our results point to an important dimension of fungal properties with likely consequences for coexistence within local communities, as well as for functional complementarity (e.g. decomposition, soil aggregation).

Highlights

  • The mycelium comprises the entirety of the hyphae of a fungus, representing its nutrient-capture and interaction interface, and the infrastructure for transport within the fungal individual

  • For lacunarity (L), we found in our study that trait values ranged between 0.4 (Basidiomycota) and 0.7 (Ascomycota)

  • It would be interesting to examine if fungal lifestyle influences the expression of the traits we examined here

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Summary

Introduction

The mycelium comprises the entirety of the hyphae of a fungus, representing its nutrient-capture and interaction interface, and the infrastructure for transport within the fungal individual. In the model organism Neurospora crassa branching angles decrease after approximately 22 h while hyphal extension rate and diameters increase. We are currently lacking a systematic comparison of a range of architectural features, measured under the same, standardized laboratory conditions, on a larger set of fungi from a common ecological context. This is why we currently only have limited knowledge about tradeoffs governing mycelium architecture that could give insight on structural “rules”. The same discrepancy holds true for the relationship between hyphal branching frequency (number of hyphal tips) and hyphal growth rate, which was examined in multiple studies focusing on Neurospora strains and mutants: some studies found a positive relationship[14] and others did not[15]

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