2017
DOI: 10.1007/s13225-017-0379-z
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Using a temporal phylogenetic method to harmonize family- and genus-level classification in the largest clade of lichen-forming fungi

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Cited by 85 publications
(94 citation statements)
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“…Our study provides the most comprehensive insight to‐date into phylogenetic relationships and biogeography in the Hypogymnioid clade in Parmeliaceae. Here, the monophyly of the four currently accepted genera in this clade was supported, as found previously with smaller ingroup taxon samplings (Divakar et al., , ; Miadlikowska et al., ). These results also supported the presence of distinct distributional patterns and clear phylogeographical structure in Hypogymnia , consistent with previous studies suggesting continental‐scale distribution in the genus (Elvebakk, ; Miadlikowska et al., ).…”
Section: Discussionsupporting
confidence: 88%
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“…Our study provides the most comprehensive insight to‐date into phylogenetic relationships and biogeography in the Hypogymnioid clade in Parmeliaceae. Here, the monophyly of the four currently accepted genera in this clade was supported, as found previously with smaller ingroup taxon samplings (Divakar et al., , ; Miadlikowska et al., ). These results also supported the presence of distinct distributional patterns and clear phylogeographical structure in Hypogymnia , consistent with previous studies suggesting continental‐scale distribution in the genus (Elvebakk, ; Miadlikowska et al., ).…”
Section: Discussionsupporting
confidence: 88%
“…In our study, we implemented the divergent time of 31.67 Ma for the Hypogymnioid node as a secondary calibration point because this age was obtained based on three lichen fossil calibrations, i.e. Alectoria , Anzia and Parmelia (Divakar et al., ), and got the age at this node as 31.43 Ma (Oligocene). Our study indicates that early diversification events of the Hypogymnia clade occurred in the Northern Hemisphere, especially North America and Europe, and then dispersed to Australia and Asia.…”
Section: Discussionmentioning
confidence: 99%
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“…In the absence of fossil evidence for the Oropogon-Sulcaria clade, we used a previously estimated rate of molecular evolution for the ITS region for Oropogon (2.43 × 10 -9 substitution/site/year; Leavitt & al., 2012b) to infer divergence times. Exploratory analyses using this substitution rate resulted in estimates that were highly congruent with recent fossil-calibrated estimates for major groups within Parmeliaceae (Divakar & al., 2017); therefore, we assumed that our rate-calibrated approach provided reasonable estimates. Substitution rates for nuLSU, ß-tubulin and MCM7 were co-estimated along the run under a uniform prior in order to avoid biasing substitution rates with improper priors.…”
Section: Methodssupporting
confidence: 69%
“…Ongoing studies into historical biogeography of lichenized fungi have benefited from the application of molecular dating techniques (Berbee & Taylor, 2010;Prieto & Wedin, 2013). The main lichenized Ascomycota lineages appeared during Carboniferous, with successive bursts of diversification into the Jurassic and Cretaceous (Prieto & Wedin, 2013;Beimforde & al., 2014;Lumbsch, 2016;Divakar & al., 2017;Lumbsch & Rikkinen, 2017). In contrast, the origin of angiosperms was estimated either in the lower Jurassic to Lower Cretaceous (Bell & al., 2005(Bell & al., , 2010, or in the Triassic to early Jurassic (Clarke & al., 2011), which suggests a corresponding relationship between the main diversification events within Lecanoromycetidae and Ostropomycetidae and their life style as epiphytes (Prieto & Wedin, 2013), mainly on angiosperms.…”
Section: Introductionmentioning
confidence: 99%