SEARCH

SEARCH BY CITATION

Table S1. Populations sampled in this study and sample sizes for genetic (pAnalysis) and phenotypic (pheAnalysis) data. The haplotypes found in each population are also detailed.

Table S2. Primer sequences and PCR conditions for amplification of plastid regions psbE-petL and rps16-trnQ. PCR conditions: initial denaturation at 94 °C for 5 min, followed by 25 cycles of denaturation at 94 °C for 30 s, annealing at 55 °C for 30 s and extension at 72 °C for 30 s, followed by a final extension at 72 °C for 30 min followed by storage at 4 °C.

Table S3. List of haplotypes.

FilenameFormatSizeDescription
BOJ_1013_sm_SUPP.doc123KSupporting info item

Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.