The respective 2c values of these genera are 33.5, 40.4, 44.2, 0.32, 1.14, and 1.00 pg [ 26, 28], when tetraploidy is accounted for in Glycine.
Furthermore, figure 4 shows that in the IR regions, GCeq values of all cycad genera are greater than 50%, except for Ceratozamia and Stangeria (with GCeq values 47.1% and 46.1%, respectively).
The Wilcoxon Matched-Pairs Signed-Ranks Test was used to test for significant differences in θ' values between all pairs of genera for which both rbcL and trnH-psbA data were available.
The relative abundances and the arcsine transformed values of all of the genera for each site are listed in Additional file 3. Using ANOVA and paired-t-tests, we compared taxa from one site to others to identify genera that were differentially distributed in one site with respect to another.
For P. contorta values of H85 were higher when Genera oil rather than paraffinic oil (Table 4) was used as a carrier of 120 mL of triclopyr tree-1 7.7 tree-1 7.7 but little vs.iation in H85 was noted between these two treatments for P. nigra (5.9 vs. 5.8 m).
However, the rates of error were higher for some individual genera, with values of up to 45% when very recent species formed nonmonophyletic clusters.
Polytomies with branch length values of zero were constructed for genera that consisted of multiple focal taxa without cytB sequences.
Relatively low values of Shannon diversity reflected the low taxonomic richness and dominance of genera such as Prevotella and Butyrivibrio within the bacteria and Methanobrevibacter within the archaea.
Comparing RC samples to OS samples, the relative abundance of genera Abiotrophia Rothia Streptococcus Capnocytophaga and Leptotrichiawere significantly lower in RC samples at p-value cutoff of 0.01.
P-values are given for the null hypothesis that the observed ranking resulted from random sampling of the same number of genera from all 88 genera.
