“…The nuclear ribosomal ITS region (including ITS1, 5.8S rRNA,and ITS2), an approximately 600‐base‐pair region frequently used in species‐level systematics for fungi, was chosen as the target gene because it has been proposed as the standard barcode for fungi and has the highest probability of successful identification for the broadest range of fungi, with the most clearly defined barcode gap between inter‐ and intraspecific variations (Schoch et al., 2012). The ITS gene was amplified by polymerase chain reactions (PCRs) using the fungal primer set of ITS1 (5′‐ NNNNNNNNNN TCCGTAGGTGAACCTGCGG‐3′) and ITS4 (5′‐TCCTCCGCTTATTGATATGC‐3′) (White, Bruns, Lee, & Taylor, 1990), where NNNNNNNNNN represents the 10‐bp barcode designed for sample identification and the ITS primers were fused with the 454 pyrosequencing adapters. The PCRs were carried out in a 20‐μl reaction mixture containing 4 μl 5× FastPfu Buffer, 0.4 μl FastPfu polymerase, 2 μl 2.5 mmol/L dNTP mix (all from Beijing TransGen Biotech Co., Ltd., Beijing, China), 0.8 μl 5 μmol/L of each primer, and 10 ng of template DNA.…”