K-Axis eukaryote Operational Taxonomic Units (OTU) table and contextual data

• Other Authors: AADC (owner), AADC, DATA OFFICER (distributor), AADC, DATA OFFICER (custodian), AU/AADC > Australian Antarctic Data Centre, Australia (hasAssociationWith), Australian Antarctic Data Centre (publisher), Australian Antarctic Division (sponsor), BISSETT, ANDREW (hasPrincipalInvestigator), CLARKE, LAURENCE J. (hasPrincipalInvestigator), CLARKE, LAURENCE J. (author), DEAGLE, BRUCE E. (collaborator), DEAGLE, BRUCE E. (hasPrincipalInvestigator), Deagle, B.E., Clarke, L.J., Bissett, A. and Bestley, S. (originator)
• Format: Dataset
• Language: unknown
• Published: Australian Ocean Data Network
• Subjects: biota; oceans; EARTH SCIENCE > BIOLOGICAL CLASSIFICATION > PROTISTS > PLANKTON; OCEANS > OCEAN CHEMISTRY > CHLOROPHYLL; SALINITY/DENSITY > SALINITY; ILLUMINA MISEQ; EUKARYOTE; 18S RIBOSOMAL RNA; ADS > Automated DNA Sequencer; NISKIN BOTTLES; CTD > Conductivity; Temperature; Depth; LABORATORY; R/V AA > R/V Aurora Australis; ACE/CRC; AMD/AU; AMD; CEOS; GEOGRAPHIC REGION > POLAR; CONTINENT > ANTARCTICA; OCEAN > SOUTHERN OCEAN > BANZARE BANK; PRINCESS ELIZABETH TROUGH; Antarc*; Antarctica; aurora australis; Southern Ocean
• Online Access: https://researchdata.edu.au/k-axis-eukaryote-contextual-data/2818221

Progress Code: completed Purpose Characterise the eukaryotic plankton community in the Kerguelen Axis region, and identify the ecological drivers of community composition. Sampling Samples were collected on board the RSV Aurora Australis between 22 January and 17 February 2016. The cruise surveyed the region south of the Kerguelen Plateau including the Princess Elizabeth Trough and BANZARE Bank in a series of eight transects covering 8165 km. Plankton communities were collected at 45 conductivity temperature depth (CTD) stations and seven additional underway stations, with biological replicates collected at two stations (52 independent sites). Surface water was sampled from 4 plus or minus 2 m depth using the uncontaminated seawater line. Deep Chlorophyll Maximum (DCM, 10-74 m) water samples were obtained using 10 L Niskin bottles mounted on a Seabird 911+ CTD. Plankton communities were size-fractionated by sequentially filtering 10 L seawater through 25 mm 20 micron (nylon) and 5 micron filters (PVDF), and 0.45 micron Sterivex filters (PVDF). Filters were stored frozen at -80 °C. DNA extraction and high-throughput sequencing DNA was extracted from half of each filter using the MoBio PowerSoil DNA Isolation kit at the Australian Genome Research Facility (AGRF, Adelaide, Australia; http://www.agrf.org.au). The V4 region of the 18S rDNA (approximately 380 bp excluding primers) was PCR-amplified using universal eukaryotic primers from all extracts and sequenced on an Illumina MiSeq v2 (2 x 250 bp paired-end) following the Ocean Sampling Day protocol (Piredda et al. 2017). Amplicon library preparation and high-throughput sequencing were carried out at the Ramaciotti Centre for Genomics (Sydney, Australia). Sequence analysis, OTU picking and assignment followed the Biomes of Australian Soil Environments (BASE) workflow (Bissett et al. 2016). Taxonomy was assigned to OTUs based on the PR2 database using the ‘classify.seqs’ command in mothur version 1.31.2 with default settings and a bootstrap cut-off of 60%. OTUs ...