Näytä suppeat kuvailutiedot

dc.contributor.authorKoskinen, Janne
dc.contributor.authorAbrego, Nerea
dc.contributor.authorVesterinen, Eero
dc.contributor.authorRoslin, Tomas
dc.contributor.authorNyman, Tommi
dc.date.accessioned2023-08-30T06:55:02Z
dc.date.available2023-08-30T06:55:02Z
dc.date.issued2023
dc.identifier.citationKoskinen, J., Abrego, N., Vesterinen, E., Roslin, T., & Nyman, T. (2023). Environmental responses of fruiting fungal communities are phylogenetically structured. <i>Ecography</i>, <i>2023</i>(10), Article e06333. <a href="https://doi.org/10.1111/ecog.06333" target="_blank">https://doi.org/10.1111/ecog.06333</a>
dc.identifier.otherCONVID_184209124
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/88771
dc.description.abstractThrough their ephemeral reproductive structures (fruiting bodies), ectomycorrhizal forest soil fungi provide a resource for a plethora of organisms. Thus, resolving what biotic and abiotic factors determine the occurrence and abundance of fruiting bodies is fundamental for understanding the dynamics of forest trophic networks. While the influence of abiotic factors such as moisture and temperature on fungal fruiting are relatively well established, little is known about how these processes interact with the evolutionary history of fungal species to determine when, where, and in which abundance fungal fruiting bodies will emerge. A specific knowledge gap relates to whether species' responses to their environment are phylogenetically structured. Here, we ask whether related fungal taxa respond similarly to climatic factors and forest habitat characteristics, and whether such correlated responses will affect the assembly of fungal fruiting communities. To resolve these questions, we fitted joint species distribution models combining data on the species composition and abundance of fungal fruiting bodies, environmental variation, and phylogenetic relationships among fungal taxa. Our results show that both site-level forest characteristics (dominant tree species and forest age) and climatic factors related to phenology (effective heat sum) greatly influence the occurrence and abundance of fruiting bodies. More importantly, while different fungal species responded unequally to their shared environment, there was a strong phylogenetic signal in their responses, so that related fungal species tended to fruit under similar environmental conditions. Thus, not only are fruiting bodies short-lived and patchily distributed, but the availability of similar resources will be further aggregated in time and space. These strong constraints on resource availability for fungus-associated taxa highlight the potential of fungus-based networks as a model system for studies on the ecology and evolution of resource–consumer relations in ephemeral systems of high spatiotemporal patchiness.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofseriesEcography
dc.rightsCC BY 4.0
dc.subject.otherforest fungi
dc.subject.otherfungivory
dc.subject.othermycorrhizal fungi
dc.subject.otherphenology
dc.subject.otherphylogenetic signal
dc.subject.otherresource variation
dc.subject.otherspatial variation
dc.subject.othertemporal variation
dc.titleEnvironmental responses of fruiting fungal communities are phylogenetically structured
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202308304808
dc.contributor.laitosBio- ja ympäristötieteiden laitosfi
dc.contributor.laitosDepartment of Biological and Environmental Scienceen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn0906-7590
dc.relation.numberinseries10
dc.relation.volume2023
dc.type.versionpublishedVersion
dc.rights.copyright© 2023 The Authors. Ecography published by John Wiley & Sons Ltd on behalf of Nordic Society Oikos
dc.rights.accesslevelopenAccessfi
dc.relation.grantnumber342374
dc.subject.ysofenologia
dc.subject.ysosienet
dc.subject.ysomykorritsasienet
dc.subject.ysofylogenetiikka
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p1200
jyx.subject.urihttp://www.yso.fi/onto/yso/p90
jyx.subject.urihttp://www.yso.fi/onto/yso/p19603
jyx.subject.urihttp://www.yso.fi/onto/yso/p28207
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.datasethttps://doi.org/10.5061/dryad.8sf7m0cqh
dc.relation.doi10.1111/ecog.06333
dc.relation.funderResearch Council of Finlanden
dc.relation.funderSuomen Akatemiafi
jyx.fundingprogramAcademy Research Fellow, AoFen
jyx.fundingprogramAkatemiatutkija, SAfi
jyx.fundinginformationJK was funded by Bätty Väänäsen rahasto, Emil Aaltosen säätiö, Olvi-säätiö and Oskar Öflunds stiftelse. JK was funded with junior researcher position by University of Eastern Finland. JK was provided with facilities and support from University of Helsinki. NA and TN received funding from Academy of Finland (grant no. 342374 and 294466, respectively).
dc.type.okmA1


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