Symbiotic status alters fungal eco‐evolutionary offspring trajectories
Aguilar‐Trigueros, C. A., Krah, F., Cornwell, W. K., Zanne, A. E., Abrego, N., Anderson, I. C., Andrew, C. J., Baldrian, P., Bässler, C., Bissett, A., Chaudhary, V. B., Chen, B., Chen, Y., Delgado‐Baquerizo, M., Deveautour, C., Egidi, E., Flores‐Moreno, H., Golan, J., Heilmann‐Clausen, J., . . . Powell, J. R. (2023). Symbiotic status alters fungal eco‐evolutionary offspring trajectories. Ecology Letters, 26(9), 1523-1534. https://doi.org/10.1111/ele.14271
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Ecology LettersAuthors
Date
2023Discipline
ResurssiviisausyhteisöEkologia ja evoluutiobiologiaSchool of Resource WisdomEcology and Evolutionary BiologyCopyright
© 2023 the Authors
Despite host-fungal symbiotic interactions being ubiquitous in all ecosystems, understanding how symbiosis has shaped the ecology and evolution of fungal spores that are involved in dispersal and colonization of their hosts has been ignored in life-history studies. We assembled a spore morphology database covering over 26,000 species of free-living to symbiotic fungi of plants, insects and humans and found more than eight orders of variation in spore size. Evolutionary transitions in symbiotic status correlated with shifts in spore size, but the strength of this effect varied widely among phyla. Symbiotic status explained more variation than climatic variables in the current distribution of spore sizes of plant-associated fungi at a global scale while the dispersal potential of their spores is more restricted compared to free-living fungi. Our work advances life-history theory by highlighting how the interaction between symbiosis and offspring morphology shapes the reproductive and dispersal strategies among living forms.
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WileyISSN Search the Publication Forum
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https://github.com/aguilart/Symbiotic-status-and-fungal-spore-sizePublication in research information system
https://converis.jyu.fi/converis/portal/detail/Publication/183653735
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Funding. This research was supported by funding from the Federal Ministry of Education and Research (BMBF) within the collaborative Project ‘Bridging in Biodiversity Science (BIBS)’ (funding number 01LC1501A) to MCR. CAAT was supported by a Feodor Lynen Fellowship from the Humboldt Foundation. MCR acknowledges support from an ERC Advanced Grant (694368). CAAT, ICA, CD, HZ, MCR and JRP were supported by the Australia-Germany Joint Research Cooperation Scheme, an initiative of Universities Australia (UA) and the Deutscher Akademischer Austauschdienst (DAAD), for the project: ‘A new tool of the trade: Trait-based approaches in fungal ecology’. JRP acknowledges support from the Australian Research Council (FT0100590). We acknowledge the contribution of the Biomes of Australian Soil Environments (BASE) consortium in the generation of data used in this publication. The BASE project was supported by funding from Bioplatforms Australia through the Australian Government National Collaborative Research Infrastructure Strategy (NCRIS). TV and PK were supported by the Czech Science Foundation (grant 21-17749S to T. Vetrovsky). Research on microbial distribution and colonization in the BKS laboratory is funded by the Australian Research Council (DP190103714). SH acknowledges funding from the German Science Foundation (grant HE6183). SNK was supported by start-up funds from the University of Tennessee, Knoxville. FTM acknowledges support from the European Research Council (ERC Grant Agreement 647038 [BIODESERT]) and Generalitat Valenciana (CIDEGENT/2018/041). AEZ acknowledges support from the National Science Foundation (DEB: 1623040, ‘MacroMycoFunc – Forming an integrated understanding of function across fungi’ and DEB: 1655759; ‘Collaborative Research: NSFDEB-NERC: Tropical dead-wood carbon fluxes: Improving carbon models by incorporating termites and microbes’). Open access funding enabled and organized by ProjektDEAL. Open Access funding enabled and organized by Projekt DEAL. ...License
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