Trace elements concentrations measured in sediment leachates from samples collected during the IN2017-V01 voyage of the RV Investigator

• Format: Dataset
• Language: unknown
• Published: Australian Ocean Data Network
• Subjects: oceans; EARTH SCIENCE > OCEANS > OCEAN CHEMISTRY > TRACE ELEMENTS; MARINE SEDIMENTS > SEDIMENT COMPOSITION; SEDIMENT CHEMISTRY; MARINE SEDIMENTS; SEDIMENT LEACH; LABORATORY; CEOS; AMD; AMD/AU; GEOGRAPHIC REGION > POLAR; OCEAN > SOUTHERN OCEAN; CONTINENT > ANTARCTICA > WILKES LAND; Antarctic; Southern Ocean; Wilkes Land; Totten Glacier; Antarc*; Antarctica
• Online Access: https://researchdata.edu.au/trace-elements-concentrations-rv-investigator/2820906

Progress Code: completed Statement: At least 2 standards and a blank were included in every batch of analysis, which typically involved 24 samples. Samples were analysed in batches of 10 and bracketed by blanks and a Quality Control (Standard, 100 ppb). Purpose These data were collected in order to determine the geochemistry of the sediment leachates, i.e., of the ‘authigenic’ fraction of the sediment. Sediment cores were collected from the East Antarctic margin, aboard the Australian Marine National Facility R/V Investigator, during the IN2017_V01 voyage from January 14th to March 5th 2017 (Armand et al., 2018). This marine geoscience expedition, named the “Sabrina Sea Floor Survey”, focused notably on studying the interactions of the Totten Glacier with the Southern Ocean through multiple glacial cycles. The cores were collected using a multi-corer (MC), were sliced every centimetre, wrapped up in plastic bags, and stored in the fridge. Back at the home laboratory (IMAS, UTAS, Hobart, Australia), sediment samples were dried in an oven at 40°C. Three hundred mg of dry sediment was then homogenised and vortexed for 10-sec with 12 mL of a reductive solution of 0.005M hydroxylamine hydrochloride (HH) / 1.5% Acetic Acid (AA) / 0.001M Na-EDTA / 0.033M NaOH, at pH 4 (Huang et al., 2021). The leach mixture was then centrifuged, and 6 mL of the supernatant solution was collected into a Teflon vial. This solution was taken to dryness, oxidized with 1 mL HNO3 + 100 µL H2O2, and redissolved in 4 mL of 7.5M HNO3. A 0.5 mL aliquot was separated from the 4 mL solution for trace metal analysis by Sector Field Inductively Coupled Mass Spectrometry (SF-ICP-MS, Thermo Fisher Scientific, Bremen, Germany) at the Central Science Laboratory (UTAS, Hobart, Australia). Indium was added as internal standard (In, 100 ppb). 88Sr, 89Y, 95Mo, 107Ag, 109Ag, 111Cd, 133Cs, 137Ba, 146Nd, 169Tm, 171Yb, 185Re, 187Re, 205Tl, 208Pb, 232Th, 238U, 23Na, 24Mg, 27Al, 31P, 32S, 42Ca, 47Ti, 51V, 52Cr, 55Mn, 56Fe, 59Co, 60Ni, 63Cu and 66Zn were ...