“…The PCR reaction systems contained 0.2 µL of rTaq (TaKaRa Co., Dalian, China; see Gu et al ., ), 1.0 µL DNA template, 2.5 µL 10_rTaq buffer (Mg 2+ free), 2.5 µL 25 m m MgCl 2 , 2.0 µL dNTPs, and 0.5 µL of each primer, with the following cycling parameters: 5 min at 94°C, followed by 35 cycles of 30 s at 94°C, 30 s at 47–58°C, and 1–2.5 min at 72°C, with a subsequent 10‐min final extension at 72°C. To avoid poor Sanger sequence qualities due to inadvertent amplification of multiple products (nontarget binding of primers), PCR products were separated by electrophoresis on a 1.0% agarose gel and gel purified using a DNA Gel Extraction Kit (Bioteke, Beijing, China; see Ma et al ., ). The purified amplicons were sent to Beijing Genomics Institute (Shenzhen, China) for sequencing.…”