Major, trace element and XRF data for sediments and fish tooth samples, from a shallow marine setting with varying redox conditions (Site U1356, Wilkes Land Margin, E.Antarctica)

Fossil fish teeth from pelagic open ocean settings are considered a robust archive for preserving the neodymium (Nd) isotopic composition of ancient seawater. However, using fossil fish teeth as an archive to reconstruct seawater Nd isotopic compositions in different sedimentary redox environments and in terrigenous-dominated, shallow marine settings is less proven. To address these uncertainties, fish tooth and sediment samples from a middle Eocene section deposited proximal to the East Antarctic margin at Integrated Ocean Drilling Program Site U1356 were analyzed for major and trace element geochemistry, and Nd isotopes. Major and trace element analyses of the sediments reveal changing redox conditions throughout deposition in a shallow marine environment. However, variations in the Nd isotopic composition and rare earth element (REE) patterns of the associated fish teeth do not correspond to redox changes in the sediments. REE patterns in fish teeth at Site U1356 carry a typical mid-REE-enriched signature. However, a consistently positive Ce anomaly marks a deviation from a pure authigenic origin of REEs to the fish tooth. Neodymium isotopic compositions of cleaned and uncleaned fish teeth fall between modern seawater and local sediments and hence could be authigenic in nature, but could also be influenced by sedimentary fluxes. We conclude that the fossil fish tooth Nd isotope proxy is not sensitive to moderate changes in pore water oxygenation. However, combined studies on sediments, pore waters, fish teeth and seawater are needed to fully understand processes driving the reconstructed signature from shallow marine sections in proximity to continental sources. This article is protected by copyright. All rights reserved.

(Table 1) Snow and ice thickness and layering at observation points of the North Pole 34 drifting station

Variability of total alkalinity in sea ice of the high-latitudinal Arctic from November 2005 to May 2006 is considered. For the bulk of one- and two-year sea ice, alkalinity dependence on salinity is described as TA = k x Sal, where k is salinity/alkalinity ratio in under-ice water. The given relationship is valid within a wide range of salinity from 0.1 psu in desalinated fraction of two-year ice to 36 psu in snow on the young ice surface. Geochemically significant deviations from the relationship noted were observed exclusively in snow and the upper layer of one-year ice. In the upper layer of one-year ice, deficiency of alkalinity is observed ( delta TA ~= -0.07 mEq/kg, or -15%). In snow on the surface of the one-year ice, alkalinity excess is formed under desalination ( delta TA is as high as 1.3 mEq/kg, or 380%). Deviations registered are caused by possibility of carbonate precipitation in form of CaCO3 x 6H2O under seawater freezing. It is shown that ice formation and the following melting might cause losses of atmospheric CO2 of up to 3 x 10**12 gC/year.