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dc.date.accessioned2023-01-31T18:31:49Z
dc.date.available2023-01-31T18:31:49Z
dc.date.created2022-04-29T12:16:57Z
dc.date.issued2022
dc.identifier.citationLunde, Lisa Fagerli Jacobsen, Rannveig Margrete Kauserud, Håvard Boddy, Lynne Nybakken, Line Sverdrup-Thygeson, Anne Birkemoe, Tone . Legacies of invertebrate exclusion and tree secondary metabolites control fungal communities in dead wood. Molecular Ecology. 2022, 31(11), 3241-3253
dc.identifier.urihttp://hdl.handle.net/10852/99518
dc.description.abstractDuring decomposition of organic matter, microbial communities may follow different successional trajectories depending on the initial environment and colonizers. The timing and order of the species arrival (assembly history) can lead to divergent communities through priority effects. We explored how assembly history and resource quality affected fungal communities and decay rate of decomposing wood, 1.5 and 4.5 years after tree felling. Additionally, we investigated the effect of invertebrate exclusion during the first two summers. We measured initial resource quality of bark and wood of aspen (Populus tremula) logs and surveyed the fungal communities by DNA metabarcoding at different times during succession. We found that gradients in fungal community composition were related to resource quality and we discuss how this may reflect different fungal life history strategies. As with previous studies, the initial amount of bark tannins was negatively correlated with wood decomposition rate over 4.5 years. The initial fungal community explained variation in community composition after 1.5, but not 4.5, years of succession. Although the assembly history of initial colonizers may cause alternative trajectories in successional communities, our results indicate that the communities may converge with the arrival of secondary colonizers. We also identified a strong legacy of invertebrate exclusion on fungal communities, even after 4.5 years of succession, thereby adding crucial knowledge on the importance of invertebrates in affecting fungal community development. By measuring and manipulating aspects of assembly history and resource quality that have rarely been studied, we expand our understanding of the complexity of fungal community dynamics.
dc.languageEN
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.titleLegacies of invertebrate exclusion and tree secondary metabolites control fungal communities in dead wood
dc.title.alternativeENEngelskEnglishLegacies of invertebrate exclusion and tree secondary metabolites control fungal communities in dead wood
dc.typeJournal article
dc.creator.authorLunde, Lisa Fagerli
dc.creator.authorJacobsen, Rannveig Margrete
dc.creator.authorKauserud, Håvard
dc.creator.authorBoddy, Lynne
dc.creator.authorNybakken, Line
dc.creator.authorSverdrup-Thygeson, Anne
dc.creator.authorBirkemoe, Tone
cristin.unitcode185,15,29,0
cristin.unitnameInstitutt for biovitenskap
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin2020087
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Molecular Ecology&rft.volume=31&rft.spage=3241&rft.date=2022
dc.identifier.jtitleMolecular Ecology
dc.identifier.volume31
dc.identifier.issue11
dc.identifier.startpage3241
dc.identifier.endpage3253
dc.identifier.doihttps://doi.org/10.1111/mec.16448
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0962-1083
dc.type.versionPublishedVersion


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