2010
DOI: 10.1016/j.fgb.2010.05.004
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A multigene molecular phylogenetic assessment of true morels (Morchella) in Turkey

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Cited by 64 publications
(65 citation statements)
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“…Helium (1 ml/min) was used as Morchella is one of the most common mushrooms in Turkey, being found in almost every region of the country. Several morphological (Solak et al, 2007) and molecular (Taşkın et al, 2010(Taşkın et al, , 2012 studies have been done to identify the species in Turkey. However, there is no detailed study on the aroma components of this mushroom.…”
Section: Methodsmentioning
confidence: 99%
“…Helium (1 ml/min) was used as Morchella is one of the most common mushrooms in Turkey, being found in almost every region of the country. Several morphological (Solak et al, 2007) and molecular (Taşkın et al, 2010(Taşkın et al, , 2012 studies have been done to identify the species in Turkey. However, there is no detailed study on the aroma components of this mushroom.…”
Section: Methodsmentioning
confidence: 99%
“…Sequences generated in recent studies (Taşkın et al 2010, 2012; O’Donnell et al 2011; Du et al 2012a, 2012b) have been recorded in this site. The scientific community not only can freely download these sequences and access information for voucher specimens and/or cultures from this website, but also can contribute their validated sequences and information to the site.…”
Section: Species Diversity In Morchellamentioning
confidence: 86%
“…Development of Genealogical Concordance Phylogenetic Species Recognition (GCPSR) (Taylor et al 2000) provided a consensus criterion for resolving species relationships among fungi, including those of morels (Dettman et al 2003; Revankar and Sutton 2010; Taşkın et al 2010, 2012; O’Donnell et al 2011; Du et al 2012a; Zeng et al 2013; Elliott et al 2014; Pildain et al 2014; Voitk et al 2014). …”
Section: Species Diversity In Morchellamentioning
confidence: 99%
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“…Mycelium was pulverized in liquid nitrogen in a mortar and total genomic DNA was extracted using the modified CTAB protocol of Gawel and Jarret [21]. One-hundred-fold diluted (20-100 ng μL −1 ) DNA extracts were used as templates in the amplification of three target sequences -ITS region (primers ITS1 and ITS4 [22]), a fragment of LSU gene (primers LR7 and LR0R [23]), and a fragment of rpb2 gene (primers RPB2-9f and RPB2-3r [24]). The PCRs, clean-up of amplification products, and bidirectional sequencing were performed as described in other survey [25].…”
Section: Methodsmentioning
confidence: 99%