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2018
DOI: 10.1017/s0024282918000397
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Four new species of Bacidia s.s. (Ramalinaceae, Lecanorales) in the Russian Far East

Abstract: The molecular phylogeny of Bacidia s.s. in the Russian Far East was investigated using 62 nucleotide sequences from the ITS nrDNA region, 22 of which were newly obtained. Phylogenetic reconstructions employed Bayesian inference and maximum likelihood searches using MrBayes and RAxML. In addition, ITS2 secondary structures added further support using Compensatory Base Changes. As a result of morphological and phylogenetic studies, four new species of Bacidia are described. Bacidia areolata sp. nov. belongs to t… Show more

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Cited by 10 publications
(32 citation statements)
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“…This study was based on fresh collections of Bacidia gathered by the authors in the field from 2013 to 2015 in the southern part of the Russian Far East (Primorskiy and Khabarovskiy Krai), and on Sakhalin and the Kurile Islands (as indicated in Gerasimova et al (2018)). The second author collected the Bacidia obtecta specimens on Sakhalin in 2017 (see details under Taxonomy).…”
Section: Specimensmentioning
confidence: 99%
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“…This study was based on fresh collections of Bacidia gathered by the authors in the field from 2013 to 2015 in the southern part of the Russian Far East (Primorskiy and Khabarovskiy Krai), and on Sakhalin and the Kurile Islands (as indicated in Gerasimova et al (2018)). The second author collected the Bacidia obtecta specimens on Sakhalin in 2017 (see details under Taxonomy).…”
Section: Specimensmentioning
confidence: 99%
“…Thallus fragments were removed to minimize the risk of contamination by, for example, lichenicolous fungi. PCR amplification, purification and sequencing were performed as described in Gerasimova et al (2018). Cycling conditions included initial denaturation at 95 °C for 2 min, 5 cycles of 95 °C for 40 s, 54 °C for 60 s, 72 °C for 90 s, 33 cycles of 95 °C for 40 s, 54 °C for 60 s, 72 °C for 90 s, and a final extension step at 72 °C for 7 min.…”
Section: Dna Extraction Pcr Amplification and Dna Sequencingmentioning
confidence: 99%
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“…Five to eight apothecia were used from fresh material not older than 5 years and thallus fragments were removed in order to minimize the risk of contamination by, for example, lichenicolous fungi. PCR amplification, purification and sequencing were performed as described in Gerasimova et al (2018). Cycling conditions included initial denaturation at 95 °C for 2 min, 5 cycles of 95 °C for 40 s, 54 °C for 60 s and 72 °C for 90 s, 33 cycles of 95 °C for 40 s, 54 °C for 60 s and 72 °C for 90 s, and a final extension step at 72 °C for 7 min.…”
Section: Methodsmentioning
confidence: 99%
“…Apothecia in the Macaronesian specimens are, however, on average somewhat paler than in the type material, although apothecial colour in the holotype varies from grey‐brown to orange‐brown to purplish black. Similar and possibly closely related species include B. areolata Gerasimova & A. Beck (colourless or pale yellow hypothecium, no crystals or radiating crystal clusters in the proper exciple, distinct 3–4‐layer zone of enlarged cell lumina along excipular edge; Gerasimova et al 2018), B. millegrana (Taylor) Zahlbr. (colourless or pale yellow hypothecium, no crystals or radiating crystal clusters in the proper exciple, distinct 2‐layer zone of enlarged cell lumina along excipular edge; Ekman 1996, p. 69), B. suffusa (Fr.)…”
Section: Taxonomymentioning
confidence: 99%