2014
DOI: 10.1007/s13225-014-0286-5
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A large-scale phylogenetic revision of Roccellaceae (Arthoniales) reveals eight new genera

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Cited by 50 publications
(68 citation statements)
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“…DNA extraction and polymerase chain reaction (PCR) amplification of Tremella specimens were performed following Millanes et al (2012). Direct PCR of Lawreya was performed following Ertz et al (2015). The PCR products were purified with Exosap in Macrogene Inc. (Amsterdam, the Netherlands).…”
Section: Dna Extraction Amplification and Sequencingmentioning
confidence: 99%
“…DNA extraction and polymerase chain reaction (PCR) amplification of Tremella specimens were performed following Millanes et al (2012). Direct PCR of Lawreya was performed following Ertz et al (2015). The PCR products were purified with Exosap in Macrogene Inc. (Amsterdam, the Netherlands).…”
Section: Dna Extraction Amplification and Sequencingmentioning
confidence: 99%
“…All the strains were fastgrowing and therefore only a few weeks were required to obtain sufficient material for DNA extraction. In some cases, hand-made sections of the hymenium or thallus were used for direct PCR as described in Ertz et al (2014). The outer wall of ascomata was removed with a sterile razor blade to isolate the hymenium.…”
Section: Molecular Techniquesmentioning
confidence: 99%
“…The possibility of this being E. sorediata was discounted in the field owing to the presence of typical S. myrticola apothecia. A sorediate, nonfertile thallus of S. myrticola has already been published from the Canary Islands but the authors had not made any link with E. sorediata (Ertz et al 2015). Since the DNA sequencing was carried out, a specimen of the sorediate morph has been collected in the New Forest from dry bark on an old Quercus with typical S. myrticola pycnidia and a Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…Well-preserved and freshly collected specimens of E. sorediata lacking any visible symptoms of fungal infection were used for DNA isolation. A small number of soredia were used for direct PCR as described in Ertz et al (2015). A targeted fragment of c. 1•1 kb at the 5′end of the nuLSU rDNA was amplified using primers LIC15R (Miadlikowska et al 2002) with LR6 (Vilgalys & Hester 1990), a fragment of c. 1 kb of the RPB2 proteincoding gene was amplified using primers fRPB2-7cF and fRPB2-11aR (Liu et al 1999), and a fragment of c. 0•6 kb of the nuITS rDNA using primers ITS1F and ITS4 (White et al 1990).…”
Section: Molecular Techniquesmentioning
confidence: 99%