Southern Ocean eDNA metabarcoding raw sequencing data, collected on the Aurora Australis 2019-2020

• 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), DEAGLE, BRUCE (hasPrincipalInvestigator), MACDONALD, ANNA (hasPrincipalInvestigator), POLANOWSKI, ANDREA (hasPrincipalInvestigator), SUTER, LEONIE (collaborator), SUTER, LEONIE (hasPrincipalInvestigator), SUTER, LEONIE (author)
• Format: Dataset
• Language: unknown
• Published: Australian Ocean Data Network
• Subjects: biota; oceans; EARTH SCIENCE > BIOLOGICAL CLASSIFICATION > ANIMALS/VERTEBRATES > FISH; ANIMALS/INVERTEBRATES > ARTHROPODS > CRUSTACEANS > EUPHAUSIIDS (KRILL); MAMMALS > CETACEANS; PCR; MISEQ; ENVIRONMENTAL DNA; METABARCODING; GENETIC SURVEY; ADS > Automated DNA Sequencer; R/V AA > R/V Aurora Australis; LABORATORY; AMD/AU; AMD; CEOS; OCEAN > SOUTHERN OCEAN; CONTINENT > ANTARCTICA; GEOGRAPHIC REGION > POLAR; Antarc*; Antarctic; Antarctica; aurora australis; Australian Antarctic Division; Southern Ocean
• Online Access: https://researchdata.edu.au/southern-ocean-edna-2019-2020/2821815

Progress Code: onGoing Purpose The purpose of this work is to determine best eDNA metabarcoding approaches to survey the Southern Ocean (SO). This includes comparisons of sampling strategy (2 L / 0.45 μm pore size filter vs 12 L / 20 μm pore size filter), PCR methodology (two step, dual MID tags vs fusion tags) and marker choice (broad range metazoan markers vs group specific markers) to develop best practice guidelines for SO surveys. On the return leg of the V1 2019 resupply voyage from Davis station to Hobart on the RSV Aurora Australis paired, open ocean environmental DNA (eDNA) samples were taken at 29 locations along the voyage. Sample names, sample coordinates as well as a range of environmental variables at each location are listed in file ‘V1 2019 Samples.xlsx’. Each sample pair consisted of one 2 L sample filtered through a 0.45 μm pore size filter, and one 12 L sample filtered through a 20 μm pore size filter. Filtering happened on board immediately after sampling. Filters of the 2 L samples were halved and stored in separate tubes, then immediately frozen at -80 ˚C. Filters of the 12 L samples were stored whole and also frozen at -80 ˚C. DNA of all samples was extracted at the specialised lab ‘eDNA frontiers’ located at Curtin University, WA using DNeasy Blood and Tissue Kits, and the extracted DNA sent back to the genetics lab at the Australian Antarctic Division (AAD). Several metabarcoding approaches were conducted to survey metazoan biodiversity present in these samples: - A marker targeting the mitochondrial gene cytochrome c oxidase I (COI) using metazoan specific primers (Forward primer mlCOIintF: GGWACWGGWTGAACWGTWTAYCCYCC; reverse primer jgHCO2198). This marker was used twice, using identical PCR conditions (95 °C for 10 min, a 16 cycle touchdown phase (62 °C -1 °C per cycle), followed by 25 cycles with an annealing temperature of 46 °C (total of 41 cycles), and a final extension at 72 °C for 5 min). : once using a two PCR step method, using MID tagged primers in the first round of PCR, ...