“…The disclosure of cryptic species strongly depends on the molecular markers used in phylogenetic identification. Currently, of the many markers that have been used in phylogenetic studies of the Glomeromycota (Błaszkowski et al, 2018a(Błaszkowski et al, ,b, 2019aJobim et al, 2019;Magurno et al, 2019), those comprising the partial small subunit (18S), internal transcribed spacer (ITS1-5.8S-ITS2 = ITS), and partial large subunit (28S) nuc rDNA segment (= 18S-ITS-28S), as well as the largest subunit of RNA polymerase II (rpb1) gene, have the highest resolution power and characterize the highest proportion of described species within the Glomeromycota (Krüger et al, 2012;Stockinger et al, 2014;Al-Yahya'ei et al, 2017). The first marker allowed to separate, for example, Rhizoglomus dunense from Rhizoglomus clarum, whose morphologies are almost identical, but sequence divergence is very high (13.3%;Al-Yahya'ei et al, 2017).…”