SRX120449 ST10.1 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293927 ST10.1 ST10.1 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120450 ST10.2 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293928 ST10.2 ST10.2 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120451 NT21.1 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293929 NT21.1 NT21.1 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120452 NT22.1 Bacteria-July2008-1 SRP010979 YarwunBacteria SRS293931 NT22.1 NT22.1 Bacteria-July2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120453 NT22.2 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293932 NT22.2 NT22.2 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120454 ST28.1 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293933 ST28.1 ST28.1 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120455 ST28.2 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293934 ST28.2 ST28.2 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120456 RT40.1 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293935 RT40.1 RT40.1 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120457 RT40.2 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293936 RT40.2 RT40.2 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120458 NT21.2 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293930 NT21.2 NT21.2 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120459 RT41.1 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293937 RT41.1 RT41.1 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120460 RT41.2 Bacteria-July 2008-1 SRP010979 YarwunBacteria SRS293938 RT41.2 RT41.2 Bacteria-July 2008-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX SRX120461 ST10.1 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293927 ST10.1 ST10.1 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120462 ST10.2 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293928 ST10.2 ST10.2 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120463 NT21.1 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293929 NT21.1 NT21.1 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120464 NT21.2 Bacteria-2009-1 SRP010979 YarwunBacteria SRS293930 NT21.2 NT21.2 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120465 NT22.1 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293931 NT22.1 NT22.1 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120466 NT22.2 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293932 NT22.2 NT22.2 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120467 ST28.1 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293933 ST28.1 ST28.1 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120468 ST28.2 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293934 ST28.2 ST28.2 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120469 RT40.1 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293935 RT40.1 RT40.1 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120470 RT40.2 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293936 RT40.2 RT40.2 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120471 RT41.1 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293937 RT41.1 RT41.1 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120472 RT41.2 Bacteria-March 2009-1 SRP010979 YarwunBacteria SRS293938 RT41.2 RT41.2 Bacteria-March 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120473 ST10.1 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293927 ST10.1 ST10.1 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120474 ST10.2 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293928 ST10.2 ST10.2 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120475 NT21.1 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293929 NT21.1 NT21.1 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120476 NT21.2 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293930 NT21.2 NT21.2 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120477 NT22.1 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293931 NT22.1 NT22.1 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120478 NT22.2 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293932 NT22.2 NT22.2 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120760 ST28.1 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293933 ST28.1 ST28.1 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120761 ST28.2 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293934 ST28.2 ST28.2 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120762 RT40.1 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293935 RT40.1 RT40.1 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120763 RT40.2 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293936 RT40.2 RT40.2 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120764 RT41.1 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293937 RT41.1 RT41.1 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120765 RT41.2 Bacteria-August 2009-1 SRP010979 YarwunBacteria SRS293938 RT41.2 RT41.2 Bacteria-August 2009-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120766 ST10.1 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293927 ST10.1 ST10.1 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120767 ST10.2 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293928 ST10.2 ST10.2 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120768 NT21.1 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293929 NT21.1 NT21.1 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120769 NT21.2 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293930 NT21.2 NT21.2 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120770 NT22.1 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293931 NT22.1 NT22.1 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120771 NT22.2 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293932 NT22.2 NT22.2 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120772 ST28.1 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293933 ST28.1 ST28.1 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120776 ST28.2 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293934 ST28.2 ST28.2 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120777 RT40.1 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293935 RT40.1 RT40.1 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120779 RT40.2 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293936 RT40.2 RT40.2 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120780 RT41.1 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293937 RT41.1 RT41.1 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX120781 RT41.2 Bacteria-March 2010-1 SRP010979 YarwunBacteria SRS293938 RT41.2 RT41.2 Bacteria-March 2010-1 AMPLICON GENOMIC PCR 0 0 Technical Read Adapter 1 1 Application Read Forward 5 454 GS FLX Titanium SRX832103 1654: F7.0.1 Bacteria-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810395 SAMN03069117 1654: F7.0.1 Bacteria-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832104 5748: F7.0.2 Bacteria-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810396 SAMN03069118 5748: F7.0.2 Bacteria-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832105 8793: F6.5.1 Bacteria-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810397 SAMN03069119 8793: F6.5.1 Bacteria-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832106 8799: F6.5.2 Bacteria-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810398 SAMN03069120 8799: F6.5.2 Bacteria-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832107 8979: F6.0.1 Bacteria-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810400 SAMN03069121 8979: F6.0.1 Bacteria-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832108 3483: F6.0.2 Bacteria-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810399 SAMN03069122 3483: F6.0.2 Bacteria-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832109 553: F5.5.1 Bacteria-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810401 SAMN03069123 553: F5.5.1 Bacteria-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832110 2935: F5.5.2 Bacteria-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810402 SAMN03069124 2935: F5.5.2 Bacteria-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832111 6204: F3.0.1 Bacteria-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810403 SAMN03069125 6204: F3.0.1 Bacteria-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832112 5008: F3.0.2 Bacteria-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810404 SAMN03069126 5008: F3.0.2 Bacteria-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832113 448: F1.0.1 Bacteria-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810405 SAMN03069127 448: F1.0.1 Bacteria-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832114 9381: F1.0.2 Bacteria-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTCCCTCGCGCCATCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- GCCTTGCCAGCCCGCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810406 SAMN03069128 9381: F1.0.2 Bacteria-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832115 3991: F7.0.1 Bacteria-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810408 SAMN03069129 3991: F7.0.1 Bacteria-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832116 5468: F7.0.2 Bacteria-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810407 SAMN03069130 5468: F7.0.2 Bacteria-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832117 2825: F6.5.1 Bacteria-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810409 SAMN03069131 2825: F6.5.1 Bacteria-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832118 1318: F6.5.2 Bacteria-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810410 SAMN03069132 1318: F6.5.2 Bacteria-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832119 6648: F6.0.1 Bacteria-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810411 SAMN03069133 6648: F6.0.1 Bacteria-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832120 1808: F6.0.2 Bacteria-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810412 SAMN03069134 1808: F6.0.2 Bacteria-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832121 1832: F5.5.1 Bacteria-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810413 SAMN03069135 1832: F5.5.1 Bacteria-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832122 5305: F5.5.2 Bacteria-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810414 SAMN03069136 5305: F5.5.2 Bacteria-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832123 62: F3.0.1 Bacteria-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810415 SAMN03069137 62: F3.0.1 Bacteria-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832124 5739: F3.0.2 Bacteria-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810416 SAMN03069138 5739: F3.0.2 Bacteria-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832125 33: F1.0.1 Bacteria-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810417 SAMN03069139 33: F1.0.1 Bacteria-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832126 174: F1.0.2 Bacteria-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810418 SAMN03069140 174: F1.0.2 Bacteria-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832127 7602: F7.0.1 Bacteria-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810419 SAMN03069141 7602: F7.0.1 Bacteria-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832128 6009: F7.0.2 Bacteria-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810421 SAMN03069142 6009: F7.0.2 Bacteria-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832129 369: F6.5.2 Bacteria-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810420 SAMN03069144 369: F6.5.2 Bacteria-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832130 6433: F3.0.1 Bacteria-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810422 SAMN03069149 6433: F3.0.1 Bacteria-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832131 3059: F1.0.1 Bacteria-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810423 SAMN03069151 3059: F1.0.1 Bacteria-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832132 7948: F1.0.2 Bacteria-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810425 SAMN03069152 7948: F1.0.2 Bacteria-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832133 2454: F7.0.1 Bacteria-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810424 SAMN03069153 2454: F7.0.1 Bacteria-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832134 3383: F7.0.2 Bacteria-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810427 SAMN03069154 3383: F7.0.2 Bacteria-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832135 8080: F6.5.1 Bacteria-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810426 SAMN03069155 8080: F6.5.1 Bacteria-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832136 9315: F6.5.2 Bacteria-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810428 SAMN03069156 9315: F6.5.2 Bacteria-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832137 7471: F6.0.1 Bacteria-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810429 SAMN03069157 7471: F6.0.1 Bacteria-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832138 3625: F6.0.2 Bacteria-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810430 SAMN03069158 3625: F6.0.2 Bacteria-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832139 8297: F5.5.1 Bacteria-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810431 SAMN03069159 8297: F5.5.1 Bacteria-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832140 6861: F5.5.2 Bacteria-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810432 SAMN03069160 6861: F5.5.2 Bacteria-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832141 8967: F3.0.1 Bacteria-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810433 SAMN03069161 8967: F3.0.1 Bacteria-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832142 406: F3.0.2 Bacteria-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810434 SAMN03069162 406: F3.0.2 Bacteria-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832143 7103: F1.0.1 Bacteria-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810435 SAMN03069163 7103: F1.0.1 Bacteria-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832144 7149: F1.0.2 Bacteria-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5'- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3', where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810436 SAMN03069164 7149: F1.0.2 Bacteria-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832145 8651: F7.0.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810437 SAMN03069165 8651: F7.0.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832146 3918: F7.0.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810438 SAMN03069166 3918: F7.0.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832147 1992: F6.5.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810439 SAMN03069167 1992: F6.5.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832148 1268: F6.5.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810440 SAMN03069168 1268: F6.5.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832149 7764: F6.0.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810441 SAMN03069169 7764: F6.0.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832150 2876: F6.0.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810442 SAMN03069170 2876: F6.0.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832151 8960: F5.5.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810443 SAMN03069171 8960: F5.5.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832152 5203: F5.5.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810445 SAMN03069172 5203: F5.5.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832153 929: F3.0.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810444 SAMN03069173 929: F3.0.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832154 1942: F3.0.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810446 SAMN03069174 1942: F3.0.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832155 9390: F1.0.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810447 SAMN03069175 9390: F1.0.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832156 3301: F1.0.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810448 SAMN03069176 3301: F1.0.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832157 1891: F7.0.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810449 SAMN03069177 1891: F7.0.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832158 1580: F7.0.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810450 SAMN03069178 1580: F7.0.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832159 2567: F6.5.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810451 SAMN03069179 2567: F6.5.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832160 5738: F6.5.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810452 SAMN03069180 5738: F6.5.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832161 4265: F6.0.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810453 SAMN03069181 4265: F6.0.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832162 713: F6.0.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810454 SAMN03069182 713: F6.0.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832163 4153: F5.5.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810456 SAMN03069183 4153: F5.5.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832164 4423: F5.5.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810455 SAMN03069184 4423: F5.5.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832165 1907: F3.0.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810457 SAMN03069185 1907: F3.0.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832166 3010: F3.0.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810458 SAMN03069186 3010: F3.0.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832167 7260: F1.0.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810459 SAMN03069187 7260: F1.0.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832168 9937: F1.0.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810460 SAMN03069188 9937: F1.0.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832169 7636: F7.0.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810461 SAMN03069189 7636: F7.0.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832170 4815: F7.0.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810462 SAMN03069190 4815: F7.0.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832171 3401: F6.5.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810463 SAMN03069192 3401: F6.5.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832172 8494: F6.0.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810464 SAMN03069194 8494: F6.0.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832173 5446: F3.0.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810465 SAMN03069197 5446: F3.0.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832174 7133: F1.0.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810466 SAMN03069199 7133: F1.0.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832175 830: F1.0.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810467 SAMN03069200 830: F1.0.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832176 7636: F7.0.1 Archaea-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810468 SAMN03069201 7636: F7.0.1 Archaea-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832177 4140: F7.0.2 Archaea-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810469 SAMN03069202 4140: F7.0.2 Archaea-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832178 1753: F6.5.1 Archaea-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810470 SAMN03069203 1753: F6.5.1 Archaea-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832179 5750: F6.5.2 Archaea-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810471 SAMN03069204 5750: F6.5.2 Archaea-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832180 4024: F6.0.1 Archaea-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810473 SAMN03069205 4024: F6.0.1 Archaea-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832181 7550: F6.0.2 Archaea-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810472 SAMN03069206 7550: F6.0.2 Archaea-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832182 1327: F5.5.1 Archaea-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810474 SAMN03069207 1327: F5.5.1 Archaea-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832183 6734: F5.5.2 Archaea-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810476 SAMN03069208 6734: F5.5.2 Archaea-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832184 7114: F3.0.1 Archaea-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810475 SAMN03069209 7114: F3.0.1 Archaea-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832185 4844: F3.0.2 Archaea-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810477 SAMN03069210 4844: F3.0.2 Archaea-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832186 1291: F1.0.1 Archaea-April 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810478 SAMN03069211 1291: F1.0.1 Archaea-April 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832187 304: F1.0.2 Archaea-April 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810479 SAMN03069212 304: F1.0.2 Archaea-April 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832188 9914: IH8.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810480 SAMN03069213 9914: IH8.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832189 6709: IH8.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810481 SAMN03069214 6709: IH8.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832190 4074: IH6.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810482 SAMN03069215 4074: IH6.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832191 5719: IH6.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810483 SAMN03069216 5719: IH6.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832192 2286: IH4.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810484 SAMN03069217 2286: IH4.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832193 8161: IH4.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810485 SAMN03069218 8161: IH4.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832194 6059: C0.25.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810486 SAMN03069219 6059: C0.25.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832195 4712: C0.25.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810487 SAMN03069220 4712: C0.25.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832196 8589: D2.0.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810488 SAMN03069221 8589: D2.0.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832197 225: D2.0.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810489 SAMN03069222 225: D2.0.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832198 4052: D5.0.1 Archaea-May 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810490 SAMN03069223 4052: D5.0.1 Archaea-May 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832199 6559: D5.0.2 Archaea-May 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810491 SAMN03069224 6559: D5.0.2 Archaea-May 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832200 8101: IH8.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810492 SAMN03069225 8101: IH8.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832201 8279: IH8.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810493 SAMN03069226 8279: IH8.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832202 8906: IH6.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810494 SAMN03069227 8906: IH6.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832203 4446: IH6.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810496 SAMN03069228 4446: IH6.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832204 2791: IH4.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810495 SAMN03069229 2791: IH4.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832205 4638: IH4.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810497 SAMN03069230 4638: IH4.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832206 4010: C0.25.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810498 SAMN03069231 4010: C0.25.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832207 6308: C0.25.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810499 SAMN03069232 6308: C0.25.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832208 8001: D2.0.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810500 SAMN03069233 8001: D2.0.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832209 2913: D2.0.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810502 SAMN03069234 2913: D2.0.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832210 4243: D5.0.1 Archaea-March 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810501 SAMN03069235 4243: D5.0.1 Archaea-March 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832211 4423: D5.0.2 Archaea-March 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810503 SAMN03069236 4423: D5.0.2 Archaea-March 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832212 9737: IH8.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810504 SAMN03069237 9737: IH8.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832213 148: IH8.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810505 SAMN03069238 148: IH8.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832214 341: IH6.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810506 SAMN03069239 341: IH6.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832215 5654: IH6.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810507 SAMN03069240 5654: IH6.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832216 8856: IH4.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810508 SAMN03069241 8856: IH4.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832217 5338: IH4.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810509 SAMN03069242 5338: IH4.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832218 8039: C0.25.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810511 SAMN03069243 8039: C0.25.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832219 95: C0.25.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810510 SAMN03069244 95: C0.25.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832220 4641: D2.0.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810512 SAMN03069245 4641: D2.0.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832221 3158: D2.0.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810514 SAMN03069246 3158: D2.0.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832222 4003: D5.0.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810513 SAMN03069247 4003: D5.0.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832223 3458: D5.0.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810515 SAMN03069248 3458: D5.0.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832224 4528: IH8.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810516 SAMN03069249 4528: IH8.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832225 145: IH8.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810517 SAMN03069250 145: IH8.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832226 471: IH6.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810518 SAMN03069251 471: IH6.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832227 948: IH6.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810519 SAMN03069252 948: IH6.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832228 4426: IH4.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810520 SAMN03069253 4426: IH4.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832229 6422: IH4.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810521 SAMN03069254 6422: IH4.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832230 2810: C0.25.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810522 SAMN03069255 2810: C0.25.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832231 4091: C0.25.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810523 SAMN03069256 4091: C0.25.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832232 8239: D2.0.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810524 SAMN03069257 8239: D2.0.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832233 6246: D2.0.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810525 SAMN03069258 6246: D2.0.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832234 6936: D5.0.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810527 SAMN03069259 6936: D5.0.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832235 7089: D5.0.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810526 SAMN03069260 7089: D5.0.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832236 9830: BB1.1 Archaea-June 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810529 SAMN03069261 9830: BB1.1 Archaea-June 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832237 3200: BB1.2 Archaea-June 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810528 SAMN03069262 3200: BB1.2 Archaea-June 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832238 53: BB2.1 Archaea-June 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810530 SAMN03069263 53: BB2.1 Archaea-June 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832239 9958: BB2.2 Archaea-June 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810531 SAMN03069264 9958: BB2.2 Archaea-June 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832240 5460: BB3.1 Archaea-June 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810532 SAMN03069265 5460: BB3.1 Archaea-June 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832241 2832: BB3.2 Archaea-June 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810533 SAMN03069266 2832: BB3.2 Archaea-June 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832242 5658: BB4.1 Archaea-June 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810534 SAMN03069267 5658: BB4.1 Archaea-June 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832243 5254: BB4.2 Archaea-June 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810535 SAMN03069268 5254: BB4.2 Archaea-June 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832244 8446: BB5.1 Archaea-June 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810536 SAMN03069269 8446: BB5.1 Archaea-June 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832245 6807: BB5.2 Archaea-June 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810537 SAMN03069270 6807: BB5.2 Archaea-June 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832246 4320: BB6.1 Archaea-June 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810538 SAMN03069271 4320: BB6.1 Archaea-June 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832247 3684: BB6.2 Archaea-June 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810539 SAMN03069272 3684: BB6.2 Archaea-June 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832248 5594: BB7.1 Archaea-June 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810540 SAMN03069273 5594: BB7.1 Archaea-June 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832249 6793: BB7.2 Archaea-June 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810541 SAMN03069274 6793: BB7.2 Archaea-June 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832250 5819: BB8.1 Archaea-June 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810542 SAMN03069275 5819: BB8.1 Archaea-June 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832251 4679: BB8.2 Archaea-June 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810543 SAMN03069276 4679: BB8.2 Archaea-June 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832252 3508: BB9.1 Archaea-June 2008-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810544 SAMN03069277 3508: BB9.1 Archaea-June 2008-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832253 2535: BB9.2 Archaea-June 2008-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810546 SAMN03069278 2535: BB9.2 Archaea-June 2008-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX SRX832254 9400: BB1.1 Archaea-June 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810545 SAMN03069279 9400: BB1.1 Archaea-June 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832255 3808: BB1.2 Archaea-June 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810547 SAMN03069280 3808: BB1.2 Archaea-June 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832256 9493: BB2.1 Archaea-June 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810548 SAMN03069281 9493: BB2.1 Archaea-June 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832257 3918: BB2.2 Archaea-June 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810549 SAMN03069282 3918: BB2.2 Archaea-June 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832258 7697: BB3.1 Archaea-June 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810550 SAMN03069283 7697: BB3.1 Archaea-June 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832259 8219: BB3.2 Archaea-June 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810551 SAMN03069284 8219: BB3.2 Archaea-June 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832260 1951: BB4.1 Archaea-June 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810552 SAMN03069285 1951: BB4.1 Archaea-June 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832261 8133: BB4.2 Archaea-June 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810554 SAMN03069286 8133: BB4.2 Archaea-June 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832262 5813: BB5.1 Archaea-June 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810553 SAMN03069287 5813: BB5.1 Archaea-June 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832263 9084: BB5.2 Archaea-June 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810555 SAMN03069288 9084: BB5.2 Archaea-June 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832264 7999: BB6.1 Archaea-June 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810556 SAMN03069289 7999: BB6.1 Archaea-June 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832265 5402: BB6.2 Archaea-June 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810557 SAMN03069290 5402: BB6.2 Archaea-June 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832266 9825: BB7.1 Archaea-June 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810559 SAMN03069291 9825: BB7.1 Archaea-June 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832267 3178: BB7.2 Archaea-June 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810558 SAMN03069292 3178: BB7.2 Archaea-June 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832268 5666: BB8.1 Archaea-June 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810560 SAMN03069293 5666: BB8.1 Archaea-June 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832269 8239: BB8.2 Archaea-June 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810562 SAMN03069294 8239: BB8.2 Archaea-June 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832270 3458: BB9.1 Archaea-June 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810561 SAMN03069295 3458: BB9.1 Archaea-June 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832271 1032: BB9.2 Archaea-June 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810563 SAMN03069296 1032: BB9.2 Archaea-June 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832272 8283: BB1.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810564 SAMN03069297 8283: BB1.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832273 2142: BB1.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810565 SAMN03069298 2142: BB1.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832274 9051: BB2.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810566 SAMN03069299 9051: BB2.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832275 5476: BB2.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810568 SAMN03069300 5476: BB2.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832276 2343: BB3.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810567 SAMN03069301 2343: BB3.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832277 7850: BB3.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810569 SAMN03069302 7850: BB3.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832278 2334: BB4.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810571 SAMN03069303 2334: BB4.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832279 1381: BB4.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810570 SAMN03069304 1381: BB4.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832280 1613: BB5.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810572 SAMN03069305 1613: BB5.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832281 3334: BB5.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810574 SAMN03069306 3334: BB5.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832282 2929: BB6.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810573 SAMN03069307 2929: BB6.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832283 5310: BB6.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810575 SAMN03069308 5310: BB6.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832284 268: BB7.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810576 SAMN03069309 268: BB7.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832285 5400: BB7.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810577 SAMN03069310 5400: BB7.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832286 7704: BB8.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810578 SAMN03069311 7704: BB8.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832287 4824: BB8.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810579 SAMN03069312 4824: BB8.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832288 6713: BB9.1 Archaea-March 2010-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810580 SAMN03069313 6713: BB9.1 Archaea-March 2010-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX832289 8233: BB9.2 Archaea-March 2010-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'-GCCTTGCCAGCCCGCTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea 958arcF primer sequence. The reverse primer sequences were 5'- GCCTTGCCAGCCCGCTCAG-CGRCGGCCATGCACCWC-3' (4B-R16SAMAJOR) and 5'- GCCTTGCCAGCCCGCTCAG-CGRCRGCCATGYACCWC-3' (4B-R16SAMINOR), where the first segment comprises the 454 adaptor and the second segment comprises each archaeal reverse primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS810581 SAMN03069314 8233: BB9.2 Archaea-March 2010-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029452 6204 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348906 SAMN01086215 6204 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029453 3354 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348907 SAMN01086216 3354 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029454 5172 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348908 SAMN01086217 5172 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029455 5755 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348909 SAMN01086218 5755 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029456 2398 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348910 SAMN01086219 2398 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029457 814 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348911 SAMN01086220 814 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029458 280 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348912 SAMN01086221 280 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029459 305 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348913 SAMN01086222 305 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029460 5472 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348914 SAMN01086223 5472 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1029461 8592 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5'CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3', where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3' and 5'-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3' , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS348916 SAMN01086225 8592 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136441 F3.0.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3’, where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3’ and 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3’ , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025049 SAMN03069198 F3.0.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136442 F3.0.2 Bacteria-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3’, where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5’- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3’, where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025048 SAMN03069150 F3.0.2 Bacteria-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136443 F5.5.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3’, where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3’ and 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3’ , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025047 SAMN03069195 F5.5.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136444 F5.5.1 Bacteria-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3’, where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5’- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3’, where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025046 SAMN03069147 F5.5.1 Bacteria-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136445 F5.5.2 Archaea-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3’, where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3’ and 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3’ , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025045 SAMN03069196 F5.5.2 Archaea-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136446 F5.5.2 Bacteria-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3’, where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5’- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3’, where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025044 SAMN03069148 F5.5.2 Bacteria-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136447 F6.0.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3’, where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3’ and 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3’ , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025043 SAMN03069193 F6.0.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136448 F6.0.1 Bacteria-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3’, where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5’- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3’, where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025042 SAMN03069145 F6.0.1 Bacteria-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136449 F6.0.2 Bacteria-August 2009-2 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3’, where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5’- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3’, where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025041 SAMN03069146 F6.0.2 Bacteria-August 2009-2 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136450 F6.5.1 Archaea-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of archaeal DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-AATTGGANTCAACGCCGG-3’, where the first segment comprises the 454 adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S archaea F16SA primer sequence. The sequences of two reverse primers (major and minor) were 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCGGCCATGCACCWC-3’ and 5’-CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGRCRGCCATGYACCWC-3’ , respectively, where the first segment comprises the 454 adaptor and the second segment comprises the 16S archaea 4B-R16SMajor or 4B-R16SMinor primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025040 SAMN03069191 F6.5.1 Archaea-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium SRX1136451 F6.5.1 Bacteria-August 2009-1 SRP010979 "The 16S rRNA V6 hypervariable region of bacterial DNA was PCR amplified using barcoded primers. The forward primer sequence was 5’-CCATCTCATCCCTGCGTGTCTCCGACTCAG-X-CAACGCGAAGAACCTTACC-3’, where the first segment comprises the 454 primer A adaptor, X denotes a unique 10-nucleotide barcode sequence for each sample, followed by the 16S bacteria A-967F primer sequence. The reverse primer sequence was 5’- CCTATCCCCTGTGTGCCTTGGCAGTCTCAG-CGACAGCCATGCANCACCT-3’, where the first segment comprises the 454 adaptor and the second segment comprises the 16S bacteria B-1046R primer sequence. Barcoded samples were purified and mixed. Purified PCR products were sequenced at the Australian Genome Research Facility, Brisbane, Australia. Sequence data were separated by barcode into individual samples." SRS1025039 SAMN03069143 F6.5.1 Bacteria-August 2009-1 AMPLICON METAGENOMIC PCR 110 0 Application Read Forward 1 454 GS FLX Titanium