Thermosalinograph data - one text file per day has been collected. Data include date, time, temperature, conductivity, salinity, location. Measurements were made on the CEAMARC voyage of the Aurora Australis - voyage 3 of the 2008-2008 summer season. See other CEAMARC metadata records for more information.

Total carbon dioxide and total alkalinity analysis of niskin bottle samples collected on CTD casts. All data have been stored in a single excel file. Measurements were made on the CEAMARC voyage of the Aurora Australis - voyage 3 of the 2008-2008 summer season. See other CEAMARC metadata records for more information.

Sea-ice cores (0.09 m internal diameter) were sampled during Polarstern voyage PS117 to the Weddell Sea during December 2018 to January 2019. Ice core measurements include position, snow thickness, ice thickness, ice core temperature and bulk-salinity profiles, macro-nutrient concentrations as well as Chlorophyll-a pigment content. In addition on each ice station downwelling (surface) and under-ice irradiances were measured with a hyperspectral radiometer.

This metadata record is a 'Parent' metadata record for ASAC project 2720. See the link for the related 'Child' metadata records. The overall objective is to characterise Southern Ocean marine ecosystems, their influence on carbon dioxide exchange with the atmosphere and the deep ocean, and their sensitivity to past and future global change including climate warming, ocean stratification, and ocean acidification from anthropogenic CO2 emissions. In particular we plan to take advantage of naturally-occurring, persistent, zonal variations in Southern Ocean primary production and biomass in the Australian Sector to investigate the effects of iron addition from natural sources, and CO2 addition from anthropogenic sources, on Southern Ocean plankton communities of differing initial structure and composition. SAZ-SENSE is a study of the sensitivity of Sub-Antarctic Zone waters to global change. A 32-day oceanographic voyage onboard Australia's ice-breaker Aurora Australis was undertaken in mid-summer (Jan 17 - Feb. 20) 2007 to examine microbial ecosystem structure and biogeochemical processes in SAZ waters west and east of Tasmania, and also in the Polar Frontal Zone south of the SAZ. The voyage brought together research teams from Australasia, Europe, and North America, and was led by the ACE CRC, CSIRO Marine and Atmospheric Research, and the Australian Antarctic Division. The overall goal is to understand the controls on Sub-Antarctic Zone productivity and carbon cycling, and to assess their sensitivity to climate change. The strategy is to compare low productivity waters west of Tasmania (areas with little phytoplankton) with higher productivity waters to the east, with a focus on the role of iron as a limiting micro-nutrient. The study also seeks to examine the effect of rising CO2 levels on phytoplankton - both via regional intercomparisons and incubation experiments. Available for download from this metadata record are various datasets collected from the voyage: - An image showing a map of the cruise track. - An excel document detailing hourly position checks of the ship. - An excel document detailing the event log for the voyage. - A word document detailing prospective papers produced from the voyage. Finally a link is available for users to access the special volume of publications produced as a result of this voyage.

---- Public Summary from Project ---- The lakes and fjords of the Vestfold Hills region of Antarctica provide unique ecosystems for studying environmental changes in Antarctica over the past 8000 years. Studies of the changes in organic matter composition in sediment cores provide information how the microbial and plankton communities have changed over time in response to varying chemical and physical conditions. Our study will provide new information about how the cycles of the biologically-important elements carbon and sulfur are linked and why some sediments can preserve large amounts of organic carbon. This information will be useful for studies of palaeoclimate and will also provide valuable insights into the processes that produce petroleum source rocks. From the abstracts of the referenced papers: Preserved ribosomal DNA of planktonic phototrophic algae was recovered from Holocene anoxic sediments of Ace Lake (Antarctica), and the ancient community members were identified based on comparative sequence analysis. The similar concentration profiles of DNA of haptophytes and their traditional lipid biomarkers (alkenones and alkenoates) revealed that fossil rDNA also served as quantitative biomarkers in this environment. The DNA data clearly revealed the presence of six novel phylotypes related to known alkenone and alkenoate-biosynthesising haptophytes with Isochrysis galbana UIO 102 as their closest relative. The relative abundance of these phylotypes changed as the lake chemistry, particularly salinity, evolved over time. Changes in the alkenone distributions reflect these population changes rather than a physiological response to salinity by a single halophyte. Using this novel palaeo-ecological approach of combining data from lipid biomarkers and preserved DNA, we showed that the post-glacial development of Ace Lake from freshwater basin to marine inlet and the present-day lacustrine saline system caused major qualitative and quantitative changes in the biodiversity of the planktonic populations over time. Post-glacial Ace Lake (Vestfold Hills, Antarctica), which was initially a freshwater lake and then an open marine system, is currently a meromictic basin with anoxic, sulfidic and methane-saturated bottom waters. Lipid and 16S ribosomal RNA gene stratigraphy of up to 10,400-year-old sediment core samples from the lake revealed that these environmentally induced chemical and physical changes caused clear shifts in the species composition of archaea and aerobic methanotrophic bacteria. The combined presence of lipids specific for methanogenic archaea and molecular remains of aerobic methanotrophic bacteria (13C-depleted delta8(14)-sterols and 16S rRNA genes) revealed that an active methane cycle occurred in Ace Lake during the last 3000 calendar years and that the extant methanotrophs were most likely introduced when it became a marine inlet (9400 y BP); rDNA sequences showed 100% sequence similarity with Methanosarcinales species from freshwater environments and were the source of sn-2- and sn3-hydroxyarchaeols. Archaeal phylotypes related to uncultivated Archaea associated with various marine environments were recovered from the present-day anoxic water column and sediments deposited during the meromictic and marine period.

Crustaceans are an important component of the Antarctic marine ecosystem. Large numbers live in or close to the sea-ice cover, using it as a refuge from predation and a source of food. However, the impact of these animals on algae that grows in the sea ice is unknown. This study is examining the diets and grazing rates of crustaceans in the Antarctic sea-ice ecosystem. These results will aid our understanding of the fate of algal production in sea-ice and will enable the construction of realistic carbon budgets for this ecosystem. This project was commenced in July 2002. A five-week voyage was undertaken on the RV Aurora Australis in October and November 2002, in the vicinity of the Mertz Glacier. Pack ice cores and sub-ice water samples were collected from 8 locations, with 3 to 5 samples of each type collected per site. The cores were sectioned in the field, melted and treated for further analysis. All samples were either preserved or frozen, depending on future requirements, and returned to Australia. Sea ice cores were processed for a range of analyses including microscopy, lipid class and fatty acid determination and stable isotope analysis. A physical description of the pack ice environment (ice type, ice thickness, snow cover, temperature profiles, salinity profiles) was also compiled. A second sampling of the pack ice occurred in Sept-Oct 2003. To date, the salinity and temperature profiles of the pack ice cores have been described and a database compiled of the physical description of the region. A large number of samples (10 sites; 5 ice/water/animal samples per site) was collected and analysis has begun of stable isotopic signatures, fatty acids, chlorophyll a and species identifications. Crustaceans have been sorted under the microscope and initial descriptions of gut contents begun. The third successful sampling trip was to the fast ice surrounding Davis Station during the 2003/04 summer. Two sites were sampled regularly, with a full suite of analyses undertaken. This will provide a temporal component to the project to complement the spatial approach used in the pack ice. Analysis of the fast ice samples is ongoing. Two more sampling trips were carried out during the 2004/05 season. The first in the pack ice offshore from Casey and the second in the fast ice at Casey. The same suite of analyses as listed above was carried out and analyses are ongoing. The download file contains five excel spreadsheets, as well as a word document which further explains data collection.

Metadata record for data from ASAC Project 2720 See the link below for public details on this project. The overall objective is to characterize Southern Ocean marine ecosystems, their influence on carbon dioxide exchange with the atmosphere and the deep ocean, and their sensitivity to past and future global change including climate warming, ocean stratification, and ocean acidification from anthropogenic CO2 emissions. In particular we plan to take advantage of naturally-occurring, persistent, zonal variations in Southern Ocean primary production and biomass in the Australian Sector to investigate the effects of iron addition from natural sources, and CO2 addition from anthropogenic sources, on Southern Ocean plankton communities of differing initial structure and composition. These samples were collected on the SAZ-SENSE scientific voyage of the Australian Antarctic Program (Voyage 3 of the Aurora Australis, 2006-2007 season). SAZ-SENSE is a study of the sensitivity of Sub-Antarctic Zone waters to global change. A 32-day oceanographic voyage onboard Australia's ice-breaker Aurora Australis was undertaken in mid-summer (Jan 17 - Feb. 20) 2007 to examine microbial ecosystem structure and biogeochemical processes in SAZ waters west and east of Tasmania, and also in the Polar Frontal Zone south of the SAZ. The voyage brought together research teams from Australasia, Europe, and North America, and was led by the ACE CRC, CSIRO Marine and Atmospheric Research, and the Australian Antarctic Division. The overall goal is to understand the controls on Sub-Antarctic Zone productivity and carbon cycling, and to assess their sensitivity to climate change. The strategy is to compare low productivity waters west of Tasmania (areas with little phytoplankton) with higher productivity waters to the east, with a focus on the role of iron as a limiting micro-nutrient. The study also seeks to examine the effect of rising CO2 levels on phytoplankton - both via regional intercomparisons and incubation experiments. The data described in this metadata record are for seawater samples collected for HPLC pigments, microscopy and flow cytometry. Samples were collected either by Niskin Bottles (on a CTD), from the ocean surface with a bucket, or via a clean seawater line (at a depth of 7 metres), directly into the onboard laboratories. Samples for microscopy were examined either with an electron microscope, or a light microscope (lugol samples). The data are presented in an excel spreadsheet, available for download at the URL given below. The 'Notes' worksheet provides further information about the data contained in the spreadsheet, including a description of column headings, units used, etc. The fields used in this dataset are: Tube Label Site CTD Niskin bottle Depth (m) Date (UT) Start Time (UT) Stop Time (UT) Latitude Longitude Lugols Glutaraldehyde fixed samples Flow Coccolithophorids Volume HPLC Volume Turner Fluorometer reading (PAR) Photosynthetically Active Radiation Temperature (degrees C) Comment

This metadata record covers ASAC projects 113, 191 and 625. (ASAC_113, ASAC_191, ASAC_625). The total lipid, fatty acid, sterol and pigment composition of water column particulates collected near the Australian Antarctic Base, Davis Station, were analysed over five summer seasons (1988-93) using capillary GC, GC-MS, TLC-FID and HPLC. Polar lipids were the dominant lipid class. Maximum lipid concentrations usually occurred in samples collected in December and January and corresponded with increased algal biomass. Both lipid profiles and microscopic observations showed significant variation in algal biomass and community structure in the water column during each season and on an interannual basis. During the period of diatom blooms (predominantly Nitzschia species) the dominant sterol and fatty acid were trans-22-dehydrocholesterol and 20:5w3, accompanied by a high 16:1w7 to 16:0 ratio. Very high polyunsaturated fatty acid and total lipid concentrations were associated with diatom blooms in the area. Bacterial markers increased late in all seasons after the summer algal blooms. Long chain C30 sterols also increased during the latter half of all seasons. Fjord samples collected in the area reflected greater biomass and diversity in algal and bacterial makers than coastal sites. Signature lipids for the alga Phaeocystis pouchetii, thought to be a major alga in Antarctic waters, were identified in field samples over the five summer seasons studied. Methods Study site Davis Base is situated on the Vestfold Hills, Antarctica and incorporates numerous lakes and fjords (Fig. 1). Samples of water column particulate matter were collected during five summer seasons (1988-93), 500 meters off-shore from Magnetic Island, situated 5 km NW of Davis. Three other sampling areas were situated in the fjords of the Vestfold hills and include two sites in Ellis Fjord, one midway along Ellis Fjord and one near Ellis Fjord mouth and one sample midway along Long Fjord (Fig. 1). These fjords are protected from the marine environment, but are both marine fjords. Davis Station and Magnetic Island were used for the weekly sample sites. The mouth of Long Fjord, the mouth of Ellis Fjord, midway down Long Fjord, the deep basin in Ellis Fjord, O'Gorman Rocks and Hawker island (ocean side) were used for monthly samples. Field collection There was an initial pilot season in 1988-89, which was followed by two more detailed studies in the summers of 1989-90 and 1990-91. Four samples was also analysed from the 1991-92 and five from the 1992-93 summer seasons. During the initial pilot study at Magnetic Island in the 1988-89 summer, three water column particle samples were taken for lipid analyses. The 1989-90 and 1990-91 summer field seasons incorporated weekly sampling of the water column particulates at Magnetic Island. The phytoplankton in the fjords were studied during the summers of 1989-90 and 1990-91. The three sites that were chosen were all sampled three times in each season. Samples were also collected during the 1989-90 and 1990-91 seasons from the Magnetic Island and Fjord site s for pigment analyses. Three and five samples were collected respectively in the 1991-92 and 1992-93 seasons. Samples were also taken for microscopic analyses. For lipid analyses 30-40 liter water column particulate samples were collected at a depth of 10 m. A Seastar or INFILTREX water sampler was used in situ to filter the water through a 14.2 cm Schleicher and Schuell glass fibre filter over a three to four hour period. All filters used during sampling were preheated in a muffle furnace at 500 degrees C overnight to minimise contamination. For pigment analyses 2 to 4 litres were filtered through glass fibre filters (4.7 cm GF/F, nominal pore size 0.7 micro meters). The samples were frozen at -20 degrees C until extraction.

Exopolysaccharide (EPS) is complex sugar made by many microbes in the Antarctic marine environment. This project seeks to understand the ecological role of microbial EPS in the Southern Ocean, where it is known to strongly influence primary production. We will investigate the chemical composition and structure of EPS obtained from Antarctic microbes, which will improve our knowledge of its ecological significance and biotechnological potential. Dataset includes the following: 1) Information on Exopolysaccharide-producing bacterial isolates, isolation sites, media used and growth conditions. 2) 16S rRNA gene sequence and fatty acid data of isolates for strain identification. 3) Exopolysaccharide chemistry data including EPS carbohydrate composition, organic acid composition, sulfate content, molecular weight. 4) Physiology of exopolysaccharide synthesis. Effects of temperature and other factors on EPS yield and glucose conversion efficiency. 5) Iron binding properties. The download file includes: 11 files File 1. Bacterial isolate 16S rRNA gene sequences obtained from Southern Ocean seawater or ice samples. The sequences are all deposited on the GenBank nucleotide (NCBI) database. Sequences are in FASTA format. File 2. Seawater and sea-ice sample information including sites samples, sample type. File 3. Data for exopolysaccharide (EPS)-producing bacteria isolated and subsequently selected for further studied. Information indicates special treatments used to obtain strains including plankton towing, filtration method, and enrichment. Identification to species level was determined by 16S rRNA gene sequence analysis. File 4. EPS-producing bacterial isolate fatty acid content determined using GC/MS procedures. File 5. Basic chemical data for EPS from Antarctic isolates including protein, sulfate, and sugar type relative content (determined by chemical procedures), molecular weight in kilodaltons and polydispersity (determined by gel-based molecular seiving). File 6 Monosaccharide unit composition determined by GC/MS of EPS from Antarctic isolates. File 7. Effect of temperature on culture viscosity and growth of EPS-producing bacterium Pseudoalteromonas sp. CAM025 as affected by temperature. File 8. Effect of temperature on EPS and cell yields and EPS synthesis efficiency (as indicated by glucose consumption) of EPS-producing bacterium Pseudoalteromonas sp. CAM025 as affected by temperature. File 9. Efficiency of copper and cadmium metal ion adsorption onto EPS from EPS-producing bacterium Pseudoalteromonas sp. CAM025. File 10. Phenotypic characteristics data for novel EPS-producing Antarctic strain CAM030. Represents type strain of Olleya marilimosa. File 11. Effect of temperature on chemical make up of EPS from EPS-producing bacterium Pseudoalteromonas sp. CAM025.

Antarctic sediments and sea-ice are important regulators in global biogeochemical and atmospheric cycles. These ecosystems contain a diverse range of bacteria whose biogeochemical roles remains largely unknown and which inhabit what are continually low temperature habitats. An integrated molecular and chemical approach will be used to investigate the coupling of microbial biogeochemical processes with community structure and cold adaptation within coastal Antarctic marine sediments and within sea-ice. Overall the project expects to make an important contribution to our understanding of biological processes within low temperature habitats. DATA SET ORGANISATION: The dataset is organised on the basis of publication and is organised on the basis of the following sections: 1. SEDIMENT SAMPLES and ISOLATES Samples collected are described in terms of location, type and where data were obtained chemical features. The designation, source, media used for cultivation and isolation and availability of sediment and other related isolates are provided. Samples included are from the following locations: Clear Lake, Pendant Lake, Scale Lake, Ace Lake, Burton Lake, Ekho Lake, Organic Lake, Deep lake and Taynaya Bay (Burke Basin), Vestfold Hills region; and the Mertz Glacier Polynya region. 2. BIOMASS and ENZYME ACTIVITY DATA Biomass, numbers and extracellular enzyme activity data are provided for Bacteria and Archaea populations from Mertz Glacier Polynya shelf sediments. 3. FATTY ACID and TETRAETHER LIPID DATA Phospholipid and tetraether lipid data are provided for Mertz Glacier Polynya shelf sediments. Whole cell fatty acid data are provided for various bacterial isolates described officially as new genera or species. 4. RNA HYBRIDISATION DATA RNA hybridisation data for Mertz Glacier Polynya sediment samples is provided, including data for oligonucleotide probes specifc for total Bacteria, Archaea, the Desulfosarcina group (class Deltaproteobacteria, sulfate reducing bacterial clade), phylum Planctomycetes, phylum Bacteroidetes (Cytophaga-Flavobacterium-Bacteroides), class Gammaproteobacteria, sulfur-oxidizing and related bacteria (a subset of class Gammaproteobacteria) and Eukaryota. 5. PHYLOGENETIC DATA 16S rRNA gene sequence data are indicated including aligned datasets for three clone libraries derived from the Mertz Glacier Polynya including GenBank accession numbers. Sequence accession numbers are provided for Vestfold Hills lake sediment samples. In addition GenBank numbers are provided for denaturing gradient gel electrophoresis band sequence data from Mertz Glacier Polynya shelf sediment. Other forms of this DGGE data (banding profile analysis) are available in reference Bowman et al. 2003 (AAD ref 10971).