“…For the Melicope / Platydesma data set, four nuclear markers [ITS, external transcribed spacer (ETS), AT103 and NIAi3 ] and two plastid markers ( trnLâtrnF and psbAâtrnH ) were amplified by the polymerase chain reaction (PCR) using a standard protocol (see Appelhans et al ., ) with primer annealing temperatures of 51â55 °C for all markers except NIAi3. Amplification of NIAi3 followed a touchdown protocol (Weeks, ). Universal primers were used for amplification: ITS (ITS2, ITS3, ITS4, ITS5a; White et al ., ; Stanford, Harden & Parks, ); ETS (Bur1, 18SâIGS; Baldwin & Markos, ; Becerra, ); AT103 (At103 forward, At103 reverse; Li et al ., ); NIAi3 (NIA3F, NIA3R; Howarth & Baum, ); trnLâtrnF (c, d, e, f; Taberlet et al ., ); and psbAâtrnH (psbA, trnH; Sang, Crawford & Stuessy, ).…”