Symbiotic status alters fungal eco-evolutionary offspring trajectories.

Autor: Aguilar-Trigueros CA; Institute of Biology, Freie Universität Berlin, Berlin, Germany.; Berlin-Brandenburg Institute of Advanced Biodiversity Research (BBIB), Berlin, Germany.; Department of Biological and Environmental Science, University of Jyväskylä, Jyvaskyla, Finland.; Hawkesbury Institute for the Environment, Western Sydney University, Penrith, New South Wales, Australia., Krah FS; Faculty of Biological Sciences, Department of Conservation Biology, Institute for Ecology, Evolution and Diversity, Goethe University Frankfurt, Frankfurt am Main, Germany., Cornwell WK; Evolution & Ecology Research Center, School of Biological, Earth, and Environmental Sciences, University of New South Wales, Sydney, New South Wales, Australia., Zanne AE; Department of Biology, University of Miami, Coral Gables, Florida, USA., Abrego N; Department of Biological and Environmental Science, University of Jyväskylä, Jyvaskyla, Finland.; Department of Agricultural Sciences, University of Helsinki, Helsinki, Finland., Anderson IC; Hawkesbury Institute for the Environment, Western Sydney University, Penrith, New South Wales, Australia., Andrew CJ; Biology Department, Oberlin College & Conservatory, Oberlin, Ohio, USA., Baldrian P; Laboratory of Environmental Microbiology, Institute of Microbiology of the Czech Academy of Sciences, Praha 4, Czech Republic., Bässler C; Faculty of Biological Sciences, Department of Conservation Biology, Institute for Ecology, Evolution and Diversity, Goethe University Frankfurt, Frankfurt am Main, Germany., Bissett A; Oceans and Atmosphere, CSIRO, Hobart, Tasmania, Australia., Chaudhary VB; Department of Environmental Studies, Dartmouth College, Hanover, New Hampshire, USA., Chen B; State Key Laboratory of Urban and Regional Ecology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, People's Republic of China.; University of Chinese Academy of Sciences, Beijing, People's Republic of China., Chen Y; College of Resources and Environmental Sciences, China Agricultural University, Beijing, People's Republic of China., Delgado-Baquerizo M; Laboratorio de Biodiversidad y Funcionamiento Ecosistémico. Instituto de Recursos Naturales y Agrobiología de Sevilla (IRNAS), CSIC, Sevilla, Spain.; Unidad Asociada CSIC-UPO (BioFun). Universidad Pablo de Olavide, Sevilla, Spain., Deveautour C; AGHYLE Research Unit, Institut Polytechnique UniLaSalle, Mont-Saint-Aignan, France., Egidi E; Hawkesbury Institute for the Environment, Western Sydney University, Penrith, New South Wales, Australia., Flores-Moreno H; Department of Biology, University of Miami, Coral Gables, Florida, USA., Golan J; Departments of Botany and Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA., Heilmann-Clausen J; Center for Macroecology, Evolution and Climate, GLOBE Institute, University of Copenhagen, Copenhagen, Denmark., Hempel S; Institute of Biology, Freie Universität Berlin, Berlin, Germany., Hu Y; Key Laboratory of Agro-ecological Processes in Subtropical Region & Changsha Research Station for Agricultural and Environmental Monitoring, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Hunan, China., Kauserud H; Evogene, Department of Biosciences, University of Oslo, Oslo, Norway., Kivlin SN; Department of Ecology and Evolution, University of Tennessee, Knoxville, Tennessee, USA., Kohout P; Laboratory of Environmental Microbiology, Institute of Microbiology of the Czech Academy of Sciences, Praha 4, Czech Republic., Lammel DR; Institute of Biology, Freie Universität Berlin, Berlin, Germany., Maestre FT; Instituto Multidisciplinar para el Estudio del Medio 'Ramon Margalef', Universidad de Alicante, Carretera de San Vicente del Raspeig s/n, Alicante, Spain.; Departamento de Ecología, Universidad de Alicante, Carretera de San Vicente del Raspeig s/n, Alicante, Spain., Pringle A; Departments of Botany and Bacteriology, University of Wisconsin-Madison, Madison, Wisconsin, USA., Purhonen J; Department of Biological and Environmental Science, University of Jyväskylä, Jyvaskyla, Finland.; Department of Music, Art and Culture Studies, University of Jyväskylä, Jyvaskyla, Finland.; School of Resource Wisdom, University of Jyväskylä, Jyvaskyla, Finland., Singh BK; Hawkesbury Institute for the Environment, Western Sydney University, Penrith, New South Wales, Australia.; Global Centre for Land Based Innovation, Western Sydney University, Penrith, New South Wales, Australia., Veresoglou SD; Institute of Biology, Freie Universität Berlin, Berlin, Germany., Větrovský T; Laboratory of Environmental Microbiology, Institute of Microbiology of the Czech Academy of Sciences, Praha 4, Czech Republic., Zhang H; Hawkesbury Institute for the Environment, Western Sydney University, Penrith, New South Wales, Australia.; College of Life Sciences, Hebei University, Baoding, China., Rillig MC; Institute of Biology, Freie Universität Berlin, Berlin, Germany.; Berlin-Brandenburg Institute of Advanced Biodiversity Research (BBIB), Berlin, Germany., Powell JR; Hawkesbury Institute for the Environment, Western Sydney University, Penrith, New South Wales, Australia.
Jazyk: angličtina
Zdroj: Ecology letters [Ecol Lett] 2023 Sep; Vol. 26 (9), pp. 1523-1534. Date of Electronic Publication: 2023 Jun 17.
DOI: 10.1111/ele.14271
Abstrakt: 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.
(© 2023 The Authors. Ecology Letters published by John Wiley & Sons Ltd.)
Databáze: MEDLINE
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