Abstract

Fungal communities often form on ephemeral substrates and dispersal is critical for the persistence of fungi among the islands that form these metacommunities. Within each substrate, competition for space and resources is vital for the local persistence of fungi. The capacity to detect and respond by dispersal away from unfavorable conditions may confer higher fitness in fungi. Informed dispersal theory posits that organisms are predicted to detect information about their surroundings which may trigger a dispersal response. As such, we expect that fungi will increase allocation to dispersal in the presence of a strong competitor.In a laboratory setting, we tested how competition with other filamentous fungi affected the development of conidial pycnidiomata (asexual fruiting bodies) in Phacidium lacerum over 10 days. Phacidium lacerum was not observed to produce more asexual fruiting bodies or produce them earlier when experiencing interspecific competition with other filamentous fungi. However, we found that a trade‐off existed between growth rate and allocation to dispersal. We also observed a defensive response to specific interspecific competitors in the form of hyphal melanization of the colony which may have an impact on the growth rate and dispersal trade‐off.Our results suggest that P. lacerum have the capacity to detect and respond to competitors by changing their allocation to dispersal and growth. However, allocation to defence may come at a cost to growth and dispersal. Thus, it is likely that optimal life history allocation in fungi constrained to ephemeral resources will depend on the competitive strength of neighbors surrounding them.

Highlights

  • Dispersal is a fundamental part of the life history of an organism

  • We observed a defensive response to specific in‐ terspecific competitors in the form of hyphal melanization of the colony which may have an impact on the growth rate and dispersal trade‐off

  • We found a significant difference in pycnidial density between treat‐ ments (Figure 2, analysis of variance (ANOVA), F4,42 = 40.95, p < 0.001)

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Summary

| INTRODUCTION

Dispersal is a fundamental part of the life history of an organism. Effective dispersal can be an adaptive response to declining resource levels (Abrams, 2000; Holt, 2008) or increasing competition (Martorell & Martinez‐Lopez 2014). The increase in allocation to dispersal in plants can be influenced by environ‐ mental stress (Martorell & Martinez‐Lopez 2014) and competitive conditions (French, Robinson, Smith, & Watts, 2017; Tabassum & Bonser, 2017), where theses adversities induce higher allocation to reproduction These results may not be directly applica‐ ble to understanding the drivers of dispersal in microbial systems. The primary form of dis‐ persal is through the production of ascomata or pycnidial conidi‐ omata (Supporting information Figure S1) emerging from the surface of infected plant material, and the subsequent release of ascospores or asexual conidia (Crous, Quaedvlieg, Hansen, Hawksworth, & Groenewald, 2014) It was chosen as a suitable species as it is capa‐ ble of developing pycnidia in vitro in a Petri dish on growth media. We predict that (a) competition will induce early reproduction in a fungal colony, and (b) competition will induce high allocation to re‐ production in a fungal colony

| MATERIALS AND METHODS
Findings
| DISCUSSION
| CONCLUSION
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