[1] The X-ray fluorescence (XRF) core scanner provides bulk-sediment chemistry data measured nondestructively at the split core sediment surface. Although this method is widely accepted, there is little known about the effects of physical properties such as density and water content on XRF core scanner data. Comparison of XRF scanner measurements from the sediment surface and dry powder samples of sediment core GeoB7920 indicates strongly reduced element intensities for the lighter elements Al and Si. We relate the lower element intensities of the measurements taken at the sediment surface to the amount of water in the sample volume analyzed by the XRF core scanner. The heavier elements K, Ca, Ti, and Fe remain relatively unaffected by the variation of any physical property within sediment core GeoB7920. Additionally, we successfully use the elemental intensity of Cl as a proxy for the seawater content in the sample volume analyzed by the XRF core scanner. This enables the establishment of a correction function for the elements Al and Si that corrects for the radiation absorption of the water content in sediment core GeoB7920 off Cape Blanc, NW Africa.
On a transect between 20° and 70°S in the eastern Atlantic Ocean and Weddell Sea, water samples from 19 hydrographic stations and bottom water from 55 surface sediment samples taken with a multiple corer were investigated for the stable carbon isotopic composition of the total dissolved inorganic carbon (δ13CΣCO2). These measurements were compared to δ13C values determined on live specimens of the benthic foraminifer Fontbotia wuellerstorfi and closely related genera from the same stations. In addition, at 16 stations the stable carbon isotope composition of sedimentary organic carbon was measured. General deepwater and bottom‐water mass circulation patterns as inferred from the δ13CΣCO2 are in close agreement with those known from other nonconservative tracers. Very low δ13C values of upper Circumpolar Deep Water (<0.3‰ Pee Dee belemnite (PDB)) in the Polar Front region and the eastern limb of the Weddell gyre coincide with nutrient maxima. However, a significant decoupling of the dissolved phosphate signal from the δ13CΣCO2 signal is indicated in the abyssal Weddell Sea. We attribute this to temperature‐dependent fractionation processes during gas exchange of surface waters with the atmosphere at sites of bottom‐water formation. Multiple corer water from the sediment/water interface is slightly δ13C depleted relative to deepwater and bottom‐water δ13ΣCO2. The surface sediment organic carbon δ13C is 3 to 4‰ lower south of the Polar Front than north of it, and the δ13Corg in freshly accumulated phytodetritus is 3 to 4‰ lower than surface sediment organic carbon δ13C. Comparison of live F. wuellerstorfi δ13C and related genera with bottom‐water δ13CΣCO2 exhibits at most stations between the Subtropical Front (≈41°S) and the southern boundary of the Antarctic Circumpolar Current (≈55°S) a significant lowering of foraminiferal δ13C values. Compilation of a mean last glacial/interglacial δ13C amplitude (Δδ13C) from six published southern ocean cores results in a shift of −0.99± 0.13‰ PDB; this shift is greater than that in all other regions. However, all of these cores are from positions close to Recent oceanic fronts. Thus, for these peripheral areas of the southern ocean, we suggest about half of the glacial/interglacial shift can be explained by varying frontal zone positions and widths accompanied by a change in mode and height of export production.
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