Planktonic foraminifera Mg/Ca paleotemperatures and oxygen isotopes of ODP Hole 175-1075C

High resolution planktonic foraminifera Mg/Ca paleotemperatures and oxygen isotopes of seawater of Ocean Drilling Program (ODP) Site 1078 (off Angola) have been reconstructed and reveal insights into the seasonal thermal evolution of the Angola Current (AC), the Angola-Benguela Front (ABF), and the Benguela Current (BC) during the last glacial (50-23.5 ka BP). Special emphasis is put on time intervals possibly associated with the North Atlantic Heinrich Stadials (HS), which are thought to lead to an accumulation of heat in the South Atlantic due to a reduction of the Atlantic Meridional Overturning Circulation (AMOC). Within dating uncertainties, Globigerinoides ruber (pink) Mg/Ca-based sea surface temperature (SST) estimates that represent southern hemisphere summer surface conditions show several warming episodes that coincide with North Atlantic HS, thus supporting the concept of the bipolar thermal seesaw. In contrast, the Mg/Ca-based temperatures of Globigerina bulloides, representing the SST of the ABF/BC system during southern hemisphere winter, show no obvious response to the North Atlantic HS in the study area. We suggest that surface water cooling during the winter season is due to enhanced upwelling or upwelling of colder water masses which has most likely mitigated a warming of the ABF/BC system during HS. We further speculate that the seasonal asymmetry in our SST record results from seasonal differences in the dominance of atmospheric and oceanic teleconnections during periods of northern high latitude cooling.

Stable carbon and oxygen isotopes from samples of the Anaximander seamounts in the eastern Mediterranean Sea

Porous seep-carbonates are exposed at mud volcanoes in the eastern Mediterranean Sea. The 13C-depleted aragonitic carbonates formed as a consequence of the anaerobic oxidation of methane in a shallow sub-surface environment. Besides the macroscopically visible cavernous fabric, extensive carbonate corrosion was revealed by detailed analysis. After erosion of the background sediments, the carbonates became exposed to oxygenated bottom waters that are periodically influenced by the release of methane and upward diffusion of hydrogen sulphide. We suggest that carbonate corrosion resulted from acidity locally produced by aerobic oxidation of methane and hydrogen sulphide in the otherwise, with respect to aragonite, oversaturated bottom waters. Although it remains to be tested whether the mechanisms of carbonate dissolution suggested herein are valid, this study reveals that a better estimate of the significance of corrosion is required to assess the amount of methane-derived carbon that is permanently fixed in seep-carbonates.