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. 2017 Feb 27;114(11):2940–2945. doi: 10.1073/pnas.1614190114

Fig. 3.

Fig. 3.

Genetic diversity and rates of evolution within subsurface microbial populations. (A) Genome nucleotide diversity (π) as measured by mapping metagenome reads onto genomes of single cells derived from 0.25 m or 1.75 m sediment depth and quantifying the number of SNPs. Taxonomic names indicate the identities of the single-cell genomes (Atribacteria, n = 7; Dehalococcoidia, n = 1; Desulfatiglans, n = 2; MBG-D, n = 2; SI Appendix, Table S3). (B) Abundance of the populations represented by the single cells as inferred by multiplying the fraction of reads within a metagenomic library that mapped to the SAGs by microscopic total cell counts from the respective sediment depths. (C) Mutation rates (µg) calculated according to µg = π/2Ne, assuming that effective population size (Ne) equals the total population size shown in B and using π and the estimated genome sizes to infer SNPs genome−1 (Materials and Methods). The dashed lines show, for comparison, the µg of growing E. coli cultures. Box-and-whisker plots are as defined in Fig. 1.