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. 2015 May 6;6:313. doi: 10.3389/fpls.2015.00313

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Copyright © 2015 Zeng, Zhou, Lei, Zeng, Liu, Liu and Xiang.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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(A) Electrophoresis graph of the polymerase chain reaction (PCR)-amplified plastid trnL(UAA) intron region. The numbers 1–11 represent different species (1- Quercus fabri, 2- Choerospondias axillaris, 3- Symplocos bogotensis, 4- Cunninghamia lanceolata, 5- Loropetalum chinense, 6- Litsea coreana, 7- Liquidambar formosana, 8- Pinus massoniana, 9- Cyclobalanopsis glauca, 10- Adinandra hainanensis, and 11- Cryptomeria japonica). (B) BLAST results of the plastid trnL(UAA) intergenic spacer/intron of the 11 different tree species; the red frames represent significantly different sequence spacers. (C) BLAST results of the plastid trnL(UAA) intron of C. glauca and Q. fabri.