This data describe a set of sea-ice and seawater physical and biochemical parameters obtained from seawater samples and ice cores drilled from land fast sea ice in the vicinity of Davis Station, East Antarctica at six different dates (stations 1-6) during late Spring 2016. Stations 1: 16 Nov. 2016 Stations 2: 21 Nov. 2016 Stations 3: 23 Nov. 2016 Stations 4: 26 Nov. 2016 Stations 5: 29 Nov. 2016 Stations 6: 02 Dec. 2016 Parameters measured: - Temperature, salinity; - Iron: Dissolved (less than 0.2um), soluble (less than 0.02um) colloidal (between 0.02 and 0.2um) and Particulate fractions (greater than 0.2um); - Macronutrients: Nitrate (NO3), nitrite (NO2), silicate (Si), phosfate (PO4) and ammonium (NH4); - Chlorophyll-a (Chla); - Particulate Organic Matter: Particulate Organic Carbon (POC) and Particulate Organic Nitrogen (PON) SW0: seawater collected at the surface SW3: seawater collected at 3m depth SW10: seawater collected at 10m depth

This dataset (provided as a series of CF-compatible netcdf file) consists of 432 consecutive maps of Antarctic landfast sea ice, derived from NASA MODIS imagery. There are 24 maps per year, spanning the 18 year period from March 2000 to Feb 2018. The data are provided in a polar stereographic projection with a latitude of true scale at 70 S (i.e., to maintain compatibility with the NSIDC polar stereographic projection).

The distribution and abundance of ice-associated copepods in the fast ice of the Australian Antarctic Territory were investigated over a distance of approximately 650 km between October and December 1995. The six sites where collections were made were: offshore from Mawson station, Larsemann Hills (including Nella Bay), Rauer Islands (ice edge near Filla Is), O'Gorman Rocks and Bluff Island near Davis Station, and Murphy Rocks in the northern Vestfold Hills. Ice cores were obtained using SIPRE ice augers. Five to ten cores were collected along transects several km in length. Thickness of sea ice and snow cover were measured at each sampling site. Chlorophyll a concentrations were determined for each core. Copepods were isolated from the melted core water and identified and counted. Zooplankton tows were also made at each site where cores were collected. Nine species of copepods were identified from the cores. However, of these, only three were recorded regularly: Paralabidocera antarctica, Drescheriella glacialis and Stephos longipes. The abundance of copepods ranged between 0 and 147/L. The highest densities were recorded at the Larsemann Hills and the lowest at Murphy Rocks. Within the cores, the highest abundances were found in the bottom 10 cm of ice, irrespective of the species. Chlorophyll a concentrations ranged between 0.9 and 373 mg/m3. Data available: excel files containing sampling dates, sampling sites and abundances (number per L) of three dominant sea ice copepods, Paralabidocera antarctica, Drescheriella glacialis, Stephos longipes. Data are presented for developmental stages (nauplii, copepodites and adults) where available. Totals are also provided. Vertical distribution in some cores is also provided. Chlorophyll a concentrations (ug/L) provided for most sites. Detailed information about each of the spreadsheets is provided below: The chlorophyll spreadsheet shows chlorophyll concentrations for 5 sites in the AAT. The column headings are: core - reference number of the core collected subsection - depth in the core in cm volume - vol of melted core water volume added - 1 L of filtered seawater for melting % original - amount of total that core water represents (i.e. minus the 1L added) aliquot - volume subsampled for chlorophyll analysis acetone - amount added (mL) for extraction 750, 664, 647, 630 - wavelengths where absorbance was measured chloro a - amount of chlorophyll a in the sample ug/L - chloro a expressed as a concentration The spatial spreadsheet shows species abundances of three copepods at 4 sites N1 to NVI - nauplius stage 1 to 6 of a species CI to CVI - copepodite stage 1 to 6 of a species F or M - female or male of copepodite stage 5 or 6 1,1 etc - cores 1 and 2 from site 1 within a major location (e.g. 2 cores close together in the Larsemann Hills) The temporal spreadsheet shows abundances over time at 2 sites (O'Gorman Rocks, Bluff Is) near Davis and two species (Paralabidocera antarctica and Drescheriella glacialis) on several sampling dates N1 to N3 - total nauplii in each of three cores (i.e. not separated into stages as above) C1 to C3 - total copepodites A1 to A3 - total adults Then at the bottom are the means of each three cores.

During the ice stations, sea ice, brine/slush, snow and under-ice water sampling were collected for CO2 concentration measurement as dissolved inorganic carbon (DIC). Ice cores were collected using a Kovacs 9 cm diameter ice corer. The ice core for DIC was cut directly after retrieval with a stainless steel folded saw. The core was cut generally into 10 cm sections (20 cm when ice cores were higher than 200 cm) and put into zip-lock polyethylene bags. Care was taken to use laboratory gloves when collecting the cores. For brine sampling, partial core holes were drilled into the ice (so called sackholes), usually to a depth of 25 cm and 50 cm. At site with flooding, brine collection was not possible, and samples of the surface slush were collected instead. Slush was collected by plastic shovel. Snow samples were also collected. Under-ice water was collected with a Teflon water sampler (GL Science Inc., Japan) 1, 3, 5 m below the bottom of the sea ice. In addition, CTD water sampling was examined at each station. The cores were taken back to the ship, and transferred to the gas tight bag (GL Science Inc., Japan), and then ice was melted at about +4 degrees C in a refrigerator. Melted samples were sub-sampled for each component. The snow samples were treated in the same manner as the sea ice samples for further analysis. The dissolved inorganic carbon (DIC) of seawater was determined by coulometry [Johnson et al. 1985] using a coulometer (CM5012, UIC Inc., Binghamton, NY, USA). DIC measurement was calibrated with reference seawater materials (Batch AG; KANSO Technos Co., Ltd., Osaka, Japan) traceable to the Certified Reference Material distributed by Prof. A. G. Dickson (Scripps Institution of Oceanography, La Jolla, CA, USA). The standard deviation for DIC calculated from 20 subsamples taken from a reference seawater material (DIC = 2084.5 micro mol L-1) was 1.4 micro mol L-1. Data available: excel files containing sampling station name, dates, and DIC concentration.

Owing to the fact that the principal investigator died before data were able to be archived, the only available data are in the form of the referenced paper, which is available as a PDF download to AAD staff only. From the referenced papers: Macquarie Island is an exposure above sea level of the Macquarie Ridge Complex, on the boundary between the Australian and Pacific plates south of New Zealand. Geodynamic reconstructions show that at ca. 12-9.5 Ma, oceanic crust of the Macquarie Island region was created at this plate boundary within a system of short spreading-ridge segments linked by large-offset transform faults. At this time, the spreading rate was slowing (less than 10 mm/yr half-spreading rate) and magmatism was waning. Probably before 5 Ma, and possibly before the extinct spreading ridge had subsided, the plate boundary became obliquely convergent, and crustal blocks were rotated, tilted, and uplifted along the ridge to form the island. Planation by marine erosion has exposed sections through the oceanic crust. The magmatism that built the oceanic crust produced melts similar in composition to the widespread normal to enriched mid-oceanic ridge basalt (N- to E-MORB) suite found in many spreading ridges, but the melts ranged beyond E-MORB to primitive, highly enriched, and silica-undersaturated compositions. These compositions form one end member of a continuum from MORB but seem not to have been derived from a MORB-source mantle, despite sharing a Pacific MORB isotopic signature. The survival of these primitive melts may be due to their origin in a slow-spreading system that must have been closing down as extension along the plate boundary gave way to transpression, putting a stop to the upwelling of asthenosphere and decompression melting. In a more energetic, faster-spreading system, mixing would have been more efficient, the presence of this end member could not easily have been inferred from its isotopic composition, and the igneous rocks would have resembled a typical N- to E-MORB suite. Macquarie Island may therefore provide a type example of magmatism at a very slow spreading ridge and a clue to the origins of E-MORB. Macquarie Island is an exposure above sea-level of part of the crest of the Macquarie Ridge. The ridge marks the Australia-Pacific plate boundary south of New Zealand, where the plate boundary has evolved progressively since Eocene times from an oceanic spreading system into a system of long transform faults linked by short spreading segments, and currently into a right-lateral strike-slip plate boundary. The rocks of Macquarie Island were formed during spreading at this plate boundary in Miocene times, and include intrusive rocks (mantle and cumulate periodites, gabbros, sheeted dolerite dyke complexes), volcanic rocks (N- to E-MORB pillow lavas, picrites, breccias, hyaloclastites), and associated sediments. A set of Macquarie Island basaltic glasses has been analysed by electron microphobe for major elements, S, Cl, and F; by Fourier transform infrared spectroscopy for H2O; by laser ablation-inductively coupled plasma mass spectrometry for trace elements; and by secondary ion mass spectrometry for Sr, Nd and Pb isotopes. Macquarie Island basaltic glasses are divided into two compositional groups according to their mg-number-K2O relationships. Near-primitive basaltic glasses (Group I) have the highest mg-number (63-69), and high Al2O3 and CaO contents at a given K2O content, and carry microphenocrysts of primitive olivine (Fo86-89.5). Their bulk compositions are used to calculate primary melt compositions in equilibrium with the most magnesian Macquarie Island olivines (Fo90.5). Fractionated, Group II, basaltic glasses are saturated with olivine + plagioclase + or - clinopyroxene, and have lower mg-number (57-67), and relatively low Al2O3 and CaO contents. Group I glasses define a seriate variation within the compositional spectrum of MORB, and extend the compositional range from N-MORB

Gas Flux over Sea Ice We observed amount of gas exchange between sea ice and atmosphere. At the ice station, semi-automated chambers developed in Japan, were used for measurement of air-sea ice CO2 flux. These chambers could be used to examine spatial variability and also temporal variability of gas flux over sea ice. Samples were also taken from the snow and ice in order to measure CH4 and VOC, however these analyses will be conducted post-voyage. This metadata record will be updated in future to reflect the analysis. The chambers are designed to be placed over a snow and sea ice. When the lid is closed, CO2 concentration was measured. The opening and closing functions of the chambers are automated and were set to a 30 minutes interval. CO2 concentration (as voltage) were recorded in the data logger (CR10X, Campbell Scientific Inc.) and downloaded after the experiments. Raw data are contained in the excel files. During the CO2 flux measurement, we collected the snow, sea ice, brine/slush and under-ice water. Snow and sea ice samples were melted after sampling in PVDF film bags (like Tedlar bags in order to avoid gas exchange with ambient air) in 4C temperature and treated for analysis. A chemical analysis for carbonate systems and VOC (water), salinity, nutrient, pigment and oxygen isotopic ratio samples will take place in Japan after the voyage for analysis. During the cruise, to examine ice growth processes, we made sea ice thin-section to classify the ice cores into granular ice, columnar ice or mixed granular and columnar ice (Eicken and Lange, 1989). The CO2 data are contained in Excel spreadsheets. These use Japanese column headings. Calcium Carbonate (CACO3.6H20) as Ikaite in Sea Ice and Snow At each listed ice station we collected sea-ice cores using a Kovacs 9cm ice corer. Cores were sectioned into 10-20cm and melted at 4 degrees C, filtered and dried for later analysis of Calcium Carbonate in a home laboratory using an ICP, which produces text file outputs (included). Also included is a spreadsheet listing the cores, and the calcium carbonate measurements.

Publicly available bathymetry and geophysical data can be used to map geomorphic features of the Antarctic continental margin and adjoining ocean basins at scales of 1:1-5 million. These data can also be used to map likely locations for some Vulnerable Marine Ecosystems. Seamounts over a certain size are readily identified and submarine canyons and mid ocean ridge central valleys which harbour hydrothermal vents can be located. Geomorphic features and their properties can be related to major habitat characteristics such as sea floor type (hard versus soft), ice keel scouring, sediment deposition or erosion and current regimes. Where more detailed data are available, shelf geomorphology can be shown to provide a guide to the distribution in the area of the shelf benthic communities recognised by Gutt (2007). The geomorphic mapping method presented here provides a layer to add to benthic bioregionalistion using readily available data. An AADC maintained copy of these data are publicly available for download from the provided URL. The master copy of these data are attached to the metadata record held at Geoscience Australia (see the provided URL).

The Antarctic Fast Ice Algae Chlorophyll-a (AFIAC) dataset is a compilation of currently available sea ice chlorophyll-a data from land-fast sea ice (i.e., excluding pack ice (see ASPeCt-Bio, Meiners et al. 2012)) cores collected at circum-Antarctic locations during the period 1970 to 2015. Data come from peer-reviewed publications, field-reports, data repositories and direct contributions by field-research teams. During all campaigns the chlorophyll-a concentration (in micrograms per litre) was measured from melted ice-core sections, using standard procedures, e.g., by melting the ice at less than 5 degrees C in the dark; filtering samples onto glassfibre filters; and fluorometric analysis according to standard protocols [Holm-Hansen et al., 1965; Evans et al., 1987]. Ice samples were melted either directly or in filtered sea water, which does not yield significant differences in chlorophyll-a concentration [Dieckmann et al., 1998]. The dataset consists of 888 geo-referenced ice cores, consisting of 5718 individual ice core sections, and including 404 full vertical profiles with a minimum of three sections. Samples/sections from the remaining cores represent: i) bottom 0.05 m only (n= 32), ii) bottom 0.1 m only (n = 301), complete cores (n = 66), as well as intermittent profiles (n = 85) with at least 3 sections but gaps in-between them. For questions about this dataset please contact: Klaus Meiners and Martin Vancoppenolle This data compilation was carried out under the auspices of the Scientific Committee on Antarctic Research - ASPeCt program and the Scientific Committee on Ocean Research (SCOR) working group on Biogeochemical Exchange Processes at the Sea-Ice Interfaces (WG-140). It also contributes to SCOR WG-152 on Measuring Essential Climate Variables in Sea Ice (ECV-Ice). An update to this dataset was submitted in September, 2018.