During the ADBEX III voyage, many samples were taken of the sea ice and snow. These samples were analysed to determine water density, with the results recorded in a physical note book that is archived at the Australian Antarctic Division. Logbook(s): - Glaciology ADBEX III Water Density Results - Glaciology ADBEX III Oxygen Isotope Sample Record

Metadata record for data from ASAC Project 1119 See the link below for public details on this project. A marked bend in the Hawaiian-Emperor seamount chain supposedly resulted from a recent major reorganization of the plate-mantle system there 50 million years ago. Although alternative mantle-driven and plate-shifting hypotheses have been proposed, no contemporaneous circum-Pacific plate events have been identified. We report reconstructions for Australia and Antarctica that reveal a major plate reorganization between 50 and 53 million years ago. Revised Pacific Ocean sea-floor reconstructions suggest that subduction of the Pacific-Izanagi spreading ridge and subsequent Marianas/Tonga-Kermadec subduction initiation may have been the ultimate causes of these events. Thus, these plate reconstructions solve long-standing continental fit problems and improve constraints on the motion between East and West Antarctica and global plate circuit closure.

Metadata record for data from ASAC Project 545 See the link below for public details on this project. From the abstract of the referenced paper: Blood was collected for haematological, red cell enzyme and red cell metabolic intermediate studies from 20 Southern elephant seals Mirounga leonina. Mean haematological values were: haemoglobin (Hb) 22.4 plus or minus 1.4 g/dl, packed cell volume (PCV) 54.2 plus or minus 3.8%, mean cell volume (MCV) 213 plus or minus 5 fl and red cell count (RCC) 2.5 x 10 to power 12 / l. Red cell morphology was unremarkable. Most of the red cell enzymes showed low activity in comparison with human red cells. Haemoglobin electrophoresis showed a typical pinniped pattern, ie two major components. Total leucocyte counts, platelet counts, and coagulation studies were within expected mammalian limits. Eosinophil counts varied from 0.5 x 10 to power 9 / l (5%-49%), and there was a very wide variation in erythrocyte sedimentation rates, from 3 to 60mm/h.

A collation of known shipwrecks and vessels lost at sea from the year 1578 until 2013 containing information on year, vessel name, country, last known location, and purpose for the journey. And a collation of recent shipping incidents from 1991 until 2016 containing information on the year of the incident, vessel name, country where known, purpose of the journey and the cause of the incident. Location - listed as nearest land mass used where known. Country - Argentina = AR; Australia = AU; Bahamas = BS; Barbados = BB; Brazil = BR; China = CN; Falkland Islands = FK; France = FR; Germany = DE; Japan = JP; Korea = KR; Liberia = LR; Malta = MT; New Zealand = NZ; Norway = NO; Panama = PA; Peru = PE; Poland = PL; Russia = RU; Spain = ES; South Africa = ZA; Sweden = SE; UK = United Kingdom; US = United States of America Nationality of tourist companies are not all included as the company (principal and sub-chartered), and the ships used, are registered across different countries, some even changing within any given year. Flag state for that year is included where known. NB: vessels ran aground mainly due to severe weather conditions or inadequate hydrographic information Information was compiled for numerous references (Argentina and Chile, 2016; ASOC, 2012; Belgium, 2009; Brazil, 2012a; Brazil, 2012b; Headland, 2009; IAATO, 2000; IAATO, 2002; IAATO, 2003; IAATO, 2011a; IAATO, 2011b; Jones, 1973; Korea, 2011; New Zealand, 2007; New Zealand, 2012a; New Zealand, 2012b; New Zealand, 2015; New Zealand et al., 2011; Norway, 2007; Norway, 2008; People's Republic of China, 2013; Poland, 2016; Reich, 1980; Sweet et al., 2015; United Kingdom, 2008; United Kingdom, 2009).

Locations of sampling sites for ASAC project 40 on voyage 7 of the Aurora Australis in the 2001/2002 season. The dataset also contains information on chlorophyll, carotenoids, coccolithophorids and species identification and counts. The voyage acronym was LOSS. There are 203 observations in the collection. These data are available via the biodiversity database. The taxa represented in this collection are (species names at time of data collection, 2001-2002): Acanthoica quattrospina Calcidiscus leptoporus Coronosphaera mediterranea Emiliania huxleyi Gephyrocapsa oceanica Pentalamina corona Syracosphaera pulchra Tetraparma pelagica Triparma columacea subsp. alata Triparma laevis subsp. ramispina Triparma strigata Umbellosphaera tenuis

This dataset contains vertical profiles of particles in the upper water column (60 m depth) at six sites. A laser optical plankton counter (LOPC) was deployed through a hole in the sea ice, or from the stern of the Aurora Australis, and lowered to 60 m, logging as it was lowered. The LOPC records particles in the size range 100 um to 20 mm, though the small aperture (7 cm x 7 cm) means that the largest particles are probably only sampled rarely. For each site, the data are presented as normalised biomass for a series of equivalent spherical diameters (ESD). ESD is based on measurements of length and width of animals likely to be sampled via the LOPC (i.e. animals that are sampled at the same time with a traditional plankton net). The data were collected on the SIPEX II voyage of the Aurora Australis, from 14/9/2012 to 16/11/2012. Sites were all located in first year pack ice; the ship would nudge up to a floe and then samples of ice, zooplankton, etc. were collected directly by working on the floe. The LOPC was either deployed through a large hole in the pack ice, or it was deployed off the stern of the AA. Method of deployment did not really have an impact on the data collected, it was more a logistical decision based on conditions.

The RAN Australian Hydrographic Service conducted hydrographic survey HI290 at Heard Island, February to March 1997. The survey dataset, which includes the Report of Survey, was provided to the Australian Antarctic Data Centre by the Australian Hydrographic Office and is available for download from a Related URL in this metadata record. The survey was lead by LT R.D.Bowden. The spatial extent given in this metadata record is that of Heard Island as the spatial extent of the survey is unknown to the Australian Antarctic Data Centre. The data are not suitable for navigation.

Instrument description: Gaseous elemental mercury (GEM) was measured at five minute intervals. GEM was collected and analysed on two parallel gold traps. While GEM was collected on one gold trap, the mercury on the other traps was simultaneously being thermally desorbed and detected by a cold vapour atomic fluorescence spectrometer. The Tekran was calibrated approximately every 24 - 48 hours using an internal Hg permeation source. The internal calibration source was checked prior to shipping the instrument to Australia using an external Hg source. The internal calibration source will be verified upon return of the instrument. Instrument Setup: This instrument was sampling from a weather protected inlet positioned ~3 m off the front port side of the Monkey Deck of the Aurora Australis, directly above the bridge. The 35m heated Teflon sample line end and filter is contained within the "Ned Kelly", a large (~30 cm diameter) stainless steel can which protects against rain, snow, sea spray and major impacts. This sample line ran 25m down to the Tekran instrument which was located in a the Met-Lab. Ar (99.999% purity) was fed into the MetLab via quarter inch Teflon tubing from the oxygen store on the Monkey deck. A 2D R.M. Young (model 5305-AQ) anemometer was also deployed at the same elevation on the aft side of the sample inlet. The anemometer was oriented with zero degrees pointed directly forward of the ship. Mean Wind speed and direction were captured using Campbell Scientific CR1000 datalogger at five-minute intervals. The files included in this dataset are the raw outputs from the Tekran 2537. They include headers, though not always at the top of the file, because headers are only written when the instrument is started or after recalibration. Also included are scanned log books containing meteorological observations, maintenance notes, and when adjustments were made to the sample line (which alters anemometer data).

Overview The aim of this project was to investigate the genetic connectivity and diversity of Antarctic benthic amphipods over fine (100's of m's), intermediate (10's of km's) and large (1000's of km's) scales, using highly variable molecular markers. To achieve this, we developed seven microsatellite markers specific to the common Antarctic amphipod species Orchomenella franklini. A total of 718 specimens of O. franklini were collected from East Antarctica. Approximately 30 specimens were collected from each site, and sites were spatially hierarchically nested - i.e. sites (separated by 100m) were nested within locations (separated by 1-30km), which were nested within 2 broad regions (separated by approx. 1400km). Each amphipod sample was genotyped for all seven microsatellite loci (although occasionally a locus would not amplify in a given sample). This dataset provides all the resultant genetic data - that is, the size of the two alleles that were amplified for each microsatellite locus, in each of 718 amphipod specimens. Data collection and analysis Please refer to the associated publication (see below) for all relevant methodology. Explanation of worksheet Sample ID- a unique code given to identify each amphipod sample (the code itself has no actual meaning). Region- the broad region of the Antarctic coast from which each sample was collected. The two regions (Casey and Davis station) are separated by approx. 1400km. Location- the locations (within a region) from which each sample was collected. The names of each location reflect actual names registered by the Australian Antarctic Division and therefore their coordinates can be pinpointed on maps held by the Australian Antarctic Division Data Centre. Locations (and corresponding sites) written in italicised typeface are considered polluted (see publication for more information on this classification). Site- the sites sampled within each location. Sites are named simply by a two -letter abbreviation of the location they are from, followed by a lowercase 'a', 'b', 'c' or 'd' representing site 1, 2, 3 etc. Microsatellite data - this provides all the microsatellite genetic data generated for each amphipod specimen. Data are presented as the allele sizes (in number of base pairs) recorded for each of the seven microsatellite loci amplified. The seven microsatellite loci are called Orcfra3, Orcfra4, Orcfra5, Orcfra6, Orcfra12, Orcfra13, Orcfra26. As O. franklini is a diploid organism, each microsatellite locus has two allele sizes (hence why there are two columns underneath each locus). A '0' signifies that a particular locus did not amplify successfully in the corresponding organism (after at least two attempts). Samples were collected from Casey station between January 2009 and March 2009, and from Davis station between November 2009 and April 2010. Genetic data was generated and analysed between April 2009 and November 2009, and between May 2010 and April 2011. Genetic data obtained from the common Antarctic amphipod species Orchomenella franklini - Genetic data obtained from the common Antarctic amphipod species Orchomenella franklini. A total of 718 specimens were collected from sites within 20 km of Casey station or Davis station. Collection dates ranged from 2009 to 2010. Each amphipod sample was genotyped for seven microsatellite loci (although occasionally a locus would not amplify in a given sample).

This metadata record was created in error and a DOI assigned to it before the error was noticed. The correct metadata record is available here: https://data.aad.gov.au/metadata/records/AAS_4015_Krill_Gonad_Transcriptome with the DOI doi:10.26179/5cd3c8fec9ad8.