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We analyzed size-specific dry mass, sinking velocity, and apparent diffusivity in field-sampled marine snow, laboratory-made aggregates formed by diatoms or coccolithophorids, and small and large zooplankton fecal pellets with naturally varying content of ballast materials. Apparent diffusivity was measured directly inside aggregates and large (millimeter-long) fecal pellets using microsensors. Large fecal pellets, collected in the coastal upwelling off Cape Blanc, Mauritania, showed the highest volume-specific dry mass and sinking velocities because of a high content of opal, carbonate, and lithogenic material (mostly Saharan dust), which together comprised ,80% of the dry mass. The average solid matter density within these large fecal pellets was 1.7 g cm 23 , whereas their excess density was 0.25 6 0.07 g cm 23 . Volume-specific dry mass of all sources of aggregates and fecal pellets ranged from 3.8 to 960 mg mm 23 , and average sinking velocities varied between 51 and 732 m d 21 . Porosity was .0.43 and .0.96 within fecal pellets and phytoplankton-derived aggregates, respectively. Averaged values of apparent diffusivity of gases within large fecal pellets and aggregates were 0.74 and 0.95 times that of the free diffusion coefficient in sea water, respectively. Ballast increases sinking velocity and, thus, also potential O 2 fluxes to sedimenting aggregates and fecal pellets. Hence, ballast minerals limit the residence time of aggregates in the water column by increasing sinking velocity, but apparent diffusivity and potential oxygen supply within aggregates are high, whereby a large fraction of labile organic carbon can be respired during sedimentation.

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.