BAS Adelie Penguin Diet

• Other Authors: DEAGLE, BRUCE (hasPrincipalInvestigator), EMMERSON, LOUISE (hasPrincipalInvestigator), MCINNES, JULIE C. (hasPrincipalInvestigator), MCINNES, JULIE C. (processor), WALUDA, CLAIRE (hasPrincipalInvestigator), DUNN, MICHAEL (hasPrincipalInvestigator), POLANOWSKI, ANDREA (processor), Australian Antarctic Data Centre (publisher)
• Format: Dataset
• Language: unknown
• Published: Australian Antarctic Data Centre
• Subjects: biota; oceans; PENGUINS; EARTH SCIENCE; BIOLOGICAL CLASSIFICATION; ANIMALS/VERTEBRATES; BIRDS; USE/FEEDING HABITATS; BIOSPHERE; ECOLOGICAL DYNAMICS; SPECIES/POPULATION INTERACTIONS; INDICATOR SPECIES; COMMUNITY DYNAMICS; ADELIE PENGUIN; DNA DIET ANALYSIS; ADS > Automated DNA Sequencer; LABORATORY; FIELD INVESTIGATION; OCEAN > ATLANTIC OCEAN > SOUTH ATLANTIC OCEAN > SOUTH ORKNEY ISLANDS; GEOGRAPHIC REGION > POLAR; CONTINENT > ANTARCTICA > SIGNY ISLAND; SOUTHERN OCEAN; Southern Ocean; South Orkney Islands; Signy Island; Adelie penguin; Antarc*; Antarctica; South Atlantic Ocean
• Online Access: https://researchdata.ands.org.au/bas-adelie-penguin-diet/1459961; https://doi.org/10.26179/5eb4e8619bf96; https://data.aad.gov.au/metadata/records/AAS_4556_BAS_Adelie_Diet; http://nla.gov.au/nla.party-617536

June 2018 Adélie penguin scats were collected from Signy Island (South Orkney Islands) during crèche (December/January) 2014/15 and 2015/16 and stored in 80% Ethanol. DNA was extracted from ~30 mg of faecal material using a Promega ‘Maxwell 16' instrument and a Maxwell® 16 Tissue DNA kit. A total of 450 samples were analysed: 30 extractions per week for 2015 and 60 per week for samples collected in 2016. Three DNA markers providing different taxonomic information were amplified from penguin faecal DNA. First, ALL faecal DNA samples were characterised using a highly conserved metazoan primer set that amplifies a region of the nuclear 18S gene. In addition, a subset of faecal samples from each year were also characterised with two other primer pairs that amplify a region of the mtDNA 16S gene to allow species-level identification for most fish (16S_Fish) and krill (16S_Krill) species respectively. During amplification of markers, the products were tagged with a unique pair of index primers allowing samples to be pooled and sequenced (2x150bp) on a MiSeq high-throughput DNA sequencer. - See Adelie Pengiun Diet CCAMLR paper for all of the primer/PCR details - See BAS Adelie 18s Krill and Fish subset excel spreadsheet for sample details. - See BAS Adelie 18s ALL samples fastq for 18s fastq files - See BAS Adelie 16s Krill subset fastq for 16s krill fastq files - See BAS Adelie Fish subset fastq for 16s fish fastq files ##################################################################################### November 2018 In addition we also amplified all 450 samples with the 16S_Fish marker. - See Adelie Experiment Details 16s Fish for sample details, plate layout, first and second round PCR and miseq sheet. - See BAS Adelie Fish ALL Samples fastq for 16s fish fastq files