2020
DOI: 10.11646/phytotaxa.477.2.6
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<p><strong><em>Termitomyces acriumbonatus</em></strong><strong> <em>sp. nov.</em> (Lyophyllaceae, Agaricales) from Pakistan</strong></p>

Abstract: Four Termitomyces samples were collected in fungal surveys during 2016–2017 at Pabbi Forest Park, Punjab, Pakistan. Detailed morphological examination showed the four collections represent a new species. The phylogenetic analyses of Internal Transcribed Spacer (ITS) and Larger Sub-Unit (LSU) genes also supported the morphology to establish the new species which we describe and illustrate in this paper. The new species, Termitomyces acriumbonatus, is characterized by a small pileus 15–30 mm diam., with pointed … Show more

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Cited by 15 publications
(9 citation statements)
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“…Primers used during amplifications were ITS1F and ITS4 for the ITS region, with LR0R and LR5 for the nuLSU region (White et al 1990; Gardes & Bruns 1993). Polymerase chain reaction (PCR) conditions adapted from those of Gardes & Bruns (1993) were followed according to Usman & Khalid (2020). The PCR amplicons were purified using a QIAquick PCR Purification Kit (Qiagen, Valencia, CA, USA) and then sent for sequencing at TsingKe, China, using the aforementioned primers.…”
Section: Methodsmentioning
confidence: 99%
“…Primers used during amplifications were ITS1F and ITS4 for the ITS region, with LR0R and LR5 for the nuLSU region (White et al 1990; Gardes & Bruns 1993). Polymerase chain reaction (PCR) conditions adapted from those of Gardes & Bruns (1993) were followed according to Usman & Khalid (2020). The PCR amplicons were purified using a QIAquick PCR Purification Kit (Qiagen, Valencia, CA, USA) and then sent for sequencing at TsingKe, China, using the aforementioned primers.…”
Section: Methodsmentioning
confidence: 99%
“…The modified CTAB method given by Zhao et al (2011) was used for the extraction of DNA from the dried specimens (Figure 2). For PCR amplifications the conditions were followed as mentioned in Usman and Khalid (2020) and the primer pair ITS1F and ITS4 for the ITS region and LR0R and LR5 for the nrLSU were selected (Gardes & Bruns, 1993; Vilgalys & Hester, 1990; White et al, 1990).…”
Section: Methodsmentioning
confidence: 99%
“…The primer pair ITS1F (Gardes & Bruns, 1993) and ITS4 (White et al, 1990) was used to amplify the internal transcribed spacer (ITS) region. Polymerase chain reaction (PCR) conditions adapted from those of Gardes and Bruns (1993) were followed according to Usman and Khalid (2020). The PCR amplicons were purified using a QIAquick PCR Purification Kit (Qiagen, Valencia, CA, USA) PCR products were sent to China, where both strands were sequenced.…”
Section: Methodsmentioning
confidence: 99%
“…The primer pair ITS1F (Gardes & Bruns, 1993) and ITS4 (White et al, 1990) was used to amplify the internal transcribed spacer (ITS) region. Polymerase chain reaction (PCR) conditions adapted from those of Gardes and Bruns (1993) were followed according to Usman and Khalid (2020).…”
Section: Dna Extraction Pcr Amplification and Sequencingmentioning
confidence: 99%