Metadata record AAS_4127_antFOCE_EnvironmentalData contains seafloor Ambient Light and ambient Seawater Temperature data sets collected at the antFOCE site during the experiment. Ambient Light data was collected using Photosynthetically Active Radiation sensors (Odyssey Dataflow 392 photo diode light meters) distributed around the antFOCE site as well as several inside the experimental chambers and open plots. Seawater Temperature data were collected using Onset Hoboware Tidbit v2 (UTBI-001) temperature loggers attached to the outside of various pieces of the underwater experimental infrastructure across the antFOCE site. Refer to antFOCE report section 2.3 for deployment, sampling and on-station analysis details. https://data.aad.gov.au/metadata/records/AAS_4127_antFOCE_Project4127 Background The antFOCE experimental system was deployed in O'Brien Bay, approximately 5 kilometres south of Casey station, East Antarctica, in the austral summer of 2014/15. Surface and sub-surface (in water below the sea ice) infrastructure allowed controlled manipulation of seawater pH levels (reduced by 0.4 pH units below ambient) in 2 chambers placed on the sea floor over natural benthic communities. Two control chambers (no pH manipulation) and two open plots (no chambers, no pH manipulation) were also sampled to compare to the pH manipulated (acidified) treatment chambers. Details of the antFOCE experiment can be found in the report – "antFOCE 2014/15 – Experimental System, Deployment, Sampling and Analysis". This report and a diagram indicating how the various antFOCE data sets relate to each other are available at: https://data.aad.gov.au/metadata/records/AAS_4127_antFOCE_Project4127

This data set was collected from a ocean acidification minicosm experiment performed at Davis Station, Antarctica during the 2014/15 summer season. It includes: - description of methods for all data collection and analyses. - environmental data logged throughout the experiment; nutrients, temperature, light climate. - carbonate chemistry data; pH (on Total scale), fugacity of CO2, dissolved inorganic carbon concentration, practical alkalinity, Omega calculations for both araganite and calcite. - product datasheet (including transmission spectra) of Osram 150W HQI-TS/NDL metal halide lamps.

Refer to antFOCE report section 4.4.5 for deployment, sampling and analysis details. https://data.aad.gov.au/metadata/records/AAS_4127_antFOCE_Project4127 One camera and flash unit was mounted on the top middle section of each chamber to take one photo of the sediment every 30 minutes. The download file contains two folders with the photos taken from the 28th of January to the 23rd of February 2015 – one for Chamber A and one for Chamber C. A video time-lapse compilation of the Chamber A images is also included. Malfunctioning cameras deployed on Chamber A and C and on B and D during this same period and at other times, meant that no useful images were obtained. Background The antFOCE experimental system was deployed in O'Brien Bay, approximately 5 kilometres south of Casey station, East Antarctica, in the austral summer of 2014/15. Surface and sub-surface (in water below the sea ice) infrastructure allowed controlled manipulation of seawater pH levels (reduced by 0.4 pH units below ambient) in 2 chambers placed on the sea floor over natural benthic communities. Two control chambers (no pH manipulation) and two open plots (no chambers, no pH manipulation) were also sampled to compare to the pH manipulated (acidified) treatment chambers. Details of the antFOCE experiment can be found in the report – "antFOCE 2014/15 – Experimental System, Deployment, Sampling and Analysis". This report and a diagram indicating how the various antFOCE data sets relate to each other are available at: https://data.aad.gov.au/metadata/records/AAS_4127_antFOCE_Project4127

The dataset lists key biogeochemical parameters measured in sea ice during the SIPEX2 voyage, including dissolved and particulate iron and other trace metals, macronutrients (silicic acid, nitrates+nitrite, phosphoric acid and ammonium), iron binding organic ligands, dissolved and particulate organic carbon, Cholophylla, thermodynamics (temperature, salinity, brine volume and Rayleigh number). All sampling bottles and equipment were decontaminated using trace metal clean techniques. Care was taken at each site to select level ice with homogeneous snow thickness. At all the stations, the same sampling procedure has been used : Firstly, snow was collected using acid cleaned low density polyethylene (LDPE) shovels and transferred into acid-cleaned 3.8 l LDPE containers (Nalgene). Snow collected was analysed for temperature, salinity, nutrients, unfiltered and filtered metals. Snow thickness was recorded with a ruler. Ice cores were collected using a non-contaminating, electropolished, stainless steel sea ice corer (140 mm internal diameter, Lichtert Industry, Belgium) driven by an electric power drill. Ice cores were collected about 10 cm away from each other to minimise between-core heterogeneity. A first core was dedicated to the temperature, salinity and Chlorophyll a (Chla). To record temperature, a temperature probe (Testo, plus or minus 0.1 degrees C accuracy) was inserted in holes freshly drilled along the core every 5 to 10 cm, depending on its length. Bulk salinity was measured for melted ice sections and for brines using a YSI incorporated Model 30 conductivity meter. Chla is processed on board using a 10 AU fluorometer (turner Designs, sunnyvale California). The total length of this core is cut in sections of 7 cm. The second core is dedicated to the POC/PON (Particulate Organic Carbon/ Particulate Organic Nitrogen), DOC (Dissolved Organic Carbon) and nutrients. Six sections of 7 cm were sub-sampled from this core. The six sections were chosen so that two top, two intermediate and two basal sections. Two cores are taken for the trace metal analysis. Those cores were directly triple bagged in plastic bags (the inner one is milli-Q washed) and frozen at -20degrees C until analysis at the laboratory. Brine samples were collected by drainage from “sack holes”. Brines and under ice seawater (~1 m deep) were collected in 1 l Nalgene LDPE bottles using an insulated peristaltic pump and acid cleaned C-flex tubing (Cole Palmer). All samples were then transported to the ship as quickly as possible to prevent further freezing. Samples were used to analyse unfiltered and filtered metals, Chla, POC/PON, nutrients and DOC. Filtration for filtered metals was completed on board using a peristaltic pump and a 0.2 microns cartridge filter. All the unfiltered and filtered metals collected were acidified (2 ppt HCl seastar) and stored at room temperature until analysis at the laboratory. Nutrients, DOC and filters for POC/PON were stored frozen at -20 degrees C until analysis at Analytical Service Tasmania, Hbart. Chla filtrations and analysis were completed on board. The file "SIPEX2 sea ice data" lists key biogeochemical parameters in sea ice cores, snow, brine and underice seawater (1m depth) collected during the SIPEX2 voyage (64.26-65.15S/116.44-120.58E) carried out between the 26th of september and 29th of october 2012. The acid-cleaning protocols for sample bottles and equipment followed the guidelines of GEOTRACES (www.geotraces.org). Contamination-free ice coring equipment developed by Lannuzel et al. (2006) was used to collect ice cores. Ice cores were triple bagged and stored at -18 degrees C until further processing in the home laboratory. Ice cores were then sectioned under a class-100 laminar flow hood (AirClean 600 PCR workstation, AirClean System) using a medical grade stainless steel bonesaw (Richards Medical), thouroughly rinsed with ultra-high purity water (18.2 MO), and ice sections were then allowed to melt at ambient

During the Antarctic Division BIOMASS Experiment III (ADBEX III) cruise of the Nella Dan (Oct - Dec 1985), sea ice cores were drilled at 13 stations. Stratigraphy of the cores recorded, along with borehole temperatures. In addition to visual notes, photographs for each of the cores were taken - the negatives of these pictures are archived with the notes made. Physical records are archived at the Australian Antarctic Division.

Minicosm design: Three successive experiments to a maximum incubation of 14 days were performed from mid November to early January in the summer of 2002/03 in a temperature controlled shipping container housing six 500 L polythene tanks or minicosms. Domes of UV transmissive PMMA in the roof of the container directly above the minicosms allowed ambient sunlight to be reflected to the tanks through tubes of anodised aluminium. These tubes reflected greater than 96% of the incident radiation irrespective of wavelength. Light perturbation to each minicosm was achieved by screening materials that attenuated UV wavelengths. UV stabilised polycarbonate removed wavelengths shorter than 400 nm, transmitting only photosynthetically active radiation (PAR) and provided the control treatment (PAR). In minicosm 2, a mylar screen removed UVB wavelengths (280 - 320 nm), providing a treatment (UVA) with PAR and UVA. Minicosms 3, 4 and 5 (UVB1, 2 and 3 respectively) were screened by borosilicate glass of 9, 5, and 3 mm thickness, transmitting ambient light (including UVR) at the equivalent water depths (ED, k=0.4) of 7.15, 5.38 and 4.97 meters respectively. Minicosm 6 (UVB4) was screened with PMMA that transmitted ambient light at an ED of 4.43 m. Light measurements: Measurements of downwelling UV and PAR were obtained using biometer and Licor sensors mounted on the roof of the minicosm container. A Macam, double grating spectroradiometer measured the spectral irradiance on the roof of the container. This was then weighted with the erythemal action spectrum and correlated to that obtained by the UV biometer. The Macam was used to measure the spectral irradiance at the cross of the UV biometer. The spectral intensity of light wavelengths were measured laterally and vertically in the minicosm screened only by UV-transmissive PMMA irradiance. These measurements were used to model the light field within the minicosm. In all other light treatments the Macam measured the spectral irradiance immediately below the water surface and in the centre of the minicosm. The model was then used to predict the spectral distribution and intensity of other light treatments. These measurements were repeated at interval throughout the season to determine whether solar elevation influenced transmission of ambient downwelling irradiance to the minicosms. UV and PAR sensors fixed to the outside of the minicosm container, together with the modelled light climates within each minicosm beneath each light treatment, predicted the quantify the light to which each experimental treatment was exposed. This work was conducted as part of ASAC project 2210. The download file contains three excel spreadsheets, plus three accompanying word documents which provide detailed methods used in the collection of these data, plus more information about the experiments. The fields in this dataset are: Day Treatment UVA UVB PAR - photosynthetically active radiation

Minicosm design: Three successive experiments to a maximum incubation of 14 days were performed from mid November to early January in the summer of 2002/03 in a temperature controlled shipping container housing six 500 L polythene tanks or minicosms. Domes of UV transmissive PMMA in the roof of the container directly above the minicosms allowed ambient sunlight to be reflected to the tanks through tubes of anodised aluminium. These tubes reflected greater than 96% of the incident radiation irrespective of wavelength. Light perturbation to each minicosm was achieved by screening materials that attenuated UV wavelengths. UV stabilised polycarbonate removed wavelengths shorter than 400 nm, transmitting only photosynthetically active radiation (PAR) and provided the control treatment (PAR). In minicosm 2, a mylar screen removed UVB wavelengths (280 - 320 nm), providing a treatment (UVA) with PAR and UVA. Minicosms 3, 4 and 5 (UVB1, 2 and 3 respectively) were screened by borosilicate glass of 9, 5, and 3 mm thickness, transmitting ambient light (including UVR) at the equivalent water depths (ED, k=0.4) of 7.15, 5.38 and 4.97 meters respectively. Minicosm 6 (UVB4) was screened with PMMA that transmitted ambient light at an ED of 4.43 m. Light measurements: Measurements of downwelling UV and PAR were obtained using biometer and Licor sensors mounted on the roof of the minicosm container. A Macam, double grating spectroradiometer measured the spectral irradiance on the roof of the container. This was then weighted with the erythemal action spectrum and correlated to that obtained by the UV biometer. The Macam was used to measure the spectral irradiance at the cross of the UV biometer. The spectral intensity of light wavelengths were measured laterally and vertically in the minicosm screened only by UV-transmissive PMMA irradiance. These measurements were used to model the light field within the minicosm. In all other light treatments the Macam measured the spectral irradiance immediately below the water surface and in the centre of the minicosm. The model was then used to predict the spectral distribution and intensity of other light treatments. These measurements were repeated at interval throughout the season to determine whether solar elevation influenced transmission of ambient downwelling irradiance to the minicosms. UV and PAR sensors fixed to the outside of the minicosm container, together with the modelled light climates within each minicosm beneath each light treatment, predicted the quantify the light to which each experimental treatment was exposed. This work was conducted as part of ASAC project 2210. The download file contains three excel spreadsheets, plus three accompanying word documents which provide detailed methods used in the collection of these data, plus more information about the experiments. The fields in this dataset are: Day Treatment Carbon Hydrogen Nitrogen C:N ratio

During the ice stations, measurements of the air CO2, concentration for CO2 flux between sea ice and atmosphere were made with the chamber technique. Air-sea ice CO2 fluxes were measured over the sea ice with semi-automated chambers. Sample air from the chamber is passed through Teflon tubes connected to non-dispersive infrared (NDIR) analyzer (Model 800, LICOR Inc., USA) that was connected to a system controller and data logger (Model 10x, Campbell Scientific Inc., USA), that controls the opening/closing of the chambers as well. During the observation period, the CO2 flux was measured under three different conditions or surface types: (1) a chamber was installed above snow; (2) over the bare ice after removing the snow; (3) slush layer after removing the snow and slush crystals. The CO2 concentration in the chamber was measured every 5 s during experiments lasting 20 minutes for each chamber. A one hour cycle of measurements therefore consist of three 20 minute periods from each chamber (i.e. surface type). Data available: excel files containing sampling station name for each spreadsheet, dates, sampling time and air CO2 concentration as output voltage from NDIR (to indicated as ppm we need to calculate, but, not yet done this process) in the air and chamber for CO2 flux measurement. Also see the record - SIPEX_II_Gas_Flux

Metadata record for data expected from ASAC Project 2767 See the link below for public details on this project. A multidisciplinary survey of the processes linking sea ice with biological elements of Antarctic marine ecosystems was conducted in winter 2007. The survey provided large-scale information on sea ice biological and physical parameters in the 100-130 degree East sector off East Antarctica. The distribution of sea ice algae and krill were measured using various methods including ice coring surveys and trawls. These measurements were complemented by shipborne measurements and an intensive sea ice sampling program. Use of an ROV was attempted but did not result in quantitative/geo-referenced data. Under-ice video files are available from the Chief-Investigator. Individual word documents are available from this metadata record for each ice station. These contain information on the ice station number, date and time of record and the parameters/ samples.

Metadata record for data from ASAC Project 933 See the link below for public details on this project. Australian Antarctic and Southern Ocean Profiling Project (AASOPP) was the outcome of a government decision in 1999 that it would carry out the necessary work to place Australia in a position to be able to prepare a submission defining the outer limit the 'extended Continental Shelf' (ECS) off the Australian Antarctic Territory (AAT). The ECS is the area of seabed/subsoil jurisdiction extending beyond the 200 nautical mile Exclusive Economic Zone, and is defined by Article 76 of the United Nations Convention on the Law of the Sea. AASOPP was set up in 2000, under the management of the Department of Finance and Administration and in consultation with the Australian Antarctic Division, to undertake the acquisition and interpretation of the data that would underpin a UN submission. Technical aspects of the work were largely the responsibility of the Australian Geological Survey Organisation and the Australian Surveying and Land Information Group (later Geoscience Australia). Marine geophysical surveys were conducted in 2001/2 and 2002/3 by the primary contractors, FUGRO Geoteam supervised by AGSO (Geoscience Australia) using the vessels Geoarctic and Polar Duke (survey numbers GA227, GA228 and GA229). Data collected were seismic reflection, sonobuoy seismic refraction, magnetic and gravity profiles. Data processing was supervised by Geoscience Australia where they are archived. Seismic data were lodged with the SCAR Seismic Data Library. Law of the Sea interpretations were lodged as part of the Australian submission to the United Nations by November, 2004 with a request not to examine the Antarctic case until requested.