Skip to main content
. 2014 Nov 19;5:594. doi: 10.3389/fmicb.2014.00594

Table 1.

Subglacial Lake Whillans sediment samples used in this study, gene amplifications, sulfate reduction rates (SRR), and quantitative-PCR gene quantification.

Sample
Gene
Sulfate Reduction Rates (SRR; pmol cm-3 d-1)b
Gene quantification (copies g-1 wet sediment)
Core Depth (cm) aprA (384 bp) dsrAB (1.9 kb) dsrA (221 bp) rdsrABa
(1.9 kb)
Without formate With formate Bacterial 16S rRNA Archaeal 16S rRNA aprA % aprA of 16S rRNAc
MC-2B 0–4 + - + + 0.42** 0.41** 3.9 × 106 2.4 × 106 9.12 × 105 14.5/23.6
MC-2B 4–8 + - + - ND ND 2.6 × 104 5.8 × 105 9.60 × 103 1.6/36.6
MC-2B 28–34 + + + - ND ND 1.2 × 105 1.4 × 106 8.42 × 103 0.6/7.3
MC-3C 2–3.5 + - + + 1.67* 1.29* 8.5 × 106 4.4 × 106 9.58 × 105 7.4/11.3
MC-3C 3.5–8 + + + + 1.20* 1.84** 2.2 × 105 9.0 × 105 2.47 × 104 2.2/11.1
MC-3C 8–16 + + + - ND ND 2.0 × 104 4.0 × 105 3.67 × 103 0.9/18

Gene amplifications from SLW sediments: “+” indicates positive amplification. “-” indicates no amplification.

aAt least one of the primer combinations amplified (Table 2).

bp value calculated by one tailed unpaired t-test, NS = not significant when compared with kills; * = significant (p < 0.05); ** = highly significant (p < 0.01); The water column was NS. ND = Not Determined.

cFirst number is % aprA with respect to total prokaryote 16S rRNA gene copies and second is with respect to total bacterial 16S rRNA from Q-PCR quantification.