SUPPLEMENTARY MATERIAL Table S1. Estimates of Θ for Euphorbia lomelii. Region abbreviations follow Figure 1 in the main text. Empirical chloroplast DNA sample sizes (NcpDNA) were used in coalescent simulations. Mean and standard deviation (Std. Dev.) of Θ-values were calculated from five independent FLUCTUATE runs. Figure S1. Small-scale survey of 30 published chloroplast DNA substitution rates for coding and noncoding gene regions from diverse taxa. Reported rates were standardized in units of substitutions per site per year (if a range rather then a point estimate was given, the midpoint value was used), and then sorted into rate categories. The modal rate category from the histogram (1.1–3.0 x 10-9) contained 12 data points, and the average of these (1.57 x 10-9) was applied to Euphorbia lomelii in the present study (see Supplementary references for papers used in this literature survey). Figure S2. Model parameters of alternative vicariance scenarios tested in Euphorbia lomelii. Region abbreviations follow Fig. 1 in the main text. Effective population sizes (Ne) for extant populations (tips on the tree) were calculated using theta values given in Table S1 and a mutation rate of 1.57 x 10-9 per year (see Fig. S1), assuming a generation time of 20 years. Effective population sizes of internal nodes are the sum of decedent population Ne values. ‘Gens’ represents the number of organismal generations since a hypothesized splitting event. Supplementary references Good-Avila SV, Souza V, Gaut BS, Eguiarte LE (2006) Timing and rate of speciation in Agave (Agavaceae). Proceedings of the National Academy of Sciences, USA, 103, 9124–9129. Lavin M, Herendeen PS, Wojciechowski MF (2005) Evolutionary rates analysis of Leguminosae implicates a rapid diversification of lineages during the Tertiary. Systematic Biology, 54, 575–594. Lynch M (1997) Mutation accumulation in nuclear, organelle, and prokaryotic transfer RNA genes. Molecular Biology and Evolution, 14, 914–925. McDaniel SF, Shaw J (2003) Phylogeographic structure and cryptic speciation in the Trans-Antarctic moss Pyrrhobryum mnioides. Evolution, 57, 205–215. Richardson JE, Pennington RT, Pennington TD, Hollingsworth PM (2001) Rapid diversification of a species-rich genus of neotropical rain forest trees. Science, 293, 2242–2245. Smith CI, Pellmyr O, Althoff DM, Balcázar-Lara M, Leebens-Mack J, Seagraves KA (2008) Pattern and timing of diversification in Yucca (Agavaceae): specialized pollination does not escalate rates of diversification. Proceedings of the Royal Society of London Series B, 275, 249–258. Sorhannus U, Fox M (1999) Synonymous and nonsynonymous substitution rates in diatoms: a comparison between chloroplast and nuclear genes. Journal of Molecular Evolution, 48, 209–212. Wilson MA, Gaut B, Clegg MT (1990) Chloroplast DNA evolves slowly in the palm family. Molecular Biology and Evolution, 7, 303–314. Wolfe KH, Li W-H, Sharp PM (1987) Rates of nucleotide substitution among plant mitochondrial, chloroplast, and nuclear DNAs. Proceedings of the National Academy of Sciences, USA, 84, 9054–9058. Xiang Q-Y, Soltis DE, Soltis PS, Manchester SR, Crawford DJ (2000) Timing the Eastern Asian-Eastern North American floristic disjunction: molecular clock corroborates paleontological estimates. Molecular Phylogenetics and Evolution, 15, 462–472. Zurawski G, Clegg MT (1987) Evolution of higher-plant chloroplast DNA-encoded genes: implications for structure-function and phylogenetic studies. Annual Review of Plant Physiology, 38, 391–418.
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