High-resolution in situ oxygen microprofiles, porewater and solid phase geochemistry from the Crimean shelf (Black Sea) from Maria S. Merian cruise MSM15/1

The outer western Crimean shelf of the Black Sea is a natural laboratory to investigate effects of stable oxic versus varying hypoxic conditions on seafloor biogeochemical processes and benthic community structure. Bottom-water oxygen concentrations ranged from normoxic (175 µmol O2/L) and hypoxic (< 63 µmol O2/L) or even anoxic/sulfidic conditions within a few kilometers' distance. Variations in oxygen concentrations between 160 and 10 µmol/L even occurred within hours close to the chemocline at 134 m water depth. Total oxygen uptake, including diffusive as well as fauna-mediated oxygen consumption, decreased from 15 mmol/m**2/d on average in the oxic zone, to 7 mmol/m**2/d on average in the hypoxic zone, correlating with changes in macrobenthos composition. Benthic diffusive oxygen uptake rates, comprising respiration of microorganisms and small meiofauna, were similar in oxic and hypoxic zones (on average 4.5 mmol/m**2/d), but declined to 1.3 mmol/m**2/d in bottom waters with oxygen concentrations below 20 µmol/L. Measurements and modeling of porewater profiles indicated that reoxidation of reduced compounds played only a minor role in diffusive oxygen uptake under the different oxygen conditions, leaving the major fraction to aerobic degradation of organic carbon. Remineralization efficiency decreased from nearly 100 % in the oxic zone, to 50 % in the oxic-hypoxic zone, to 10 % in the hypoxic-anoxic zone. Overall, the faunal remineralization rate was more important, but also more influenced by fluctuating oxygen concentrations, than microbial and geochemical oxidation processes.

Stable isotope ratios of foraminifera from the continental shelf off Troms, Northern Norway

A stable oxygen and carbon isotope stratigraphy is established for a Late Weichselian/Holocene glaciomarine/marine seguence in Andfjorden and Malangsdjupet on the continental shelf off Troms, Northern Norway. The stratigraphy demonstrates that the global signals, Termination I B and possibly also I A (upper parts), are present and radiocarbon date to 10.3-9.7 kyr B.P. and >14-13.5 kyr B.P., respectively. A temperature increase of 5°-6°C and possibly a small salinity increase occurred during Term. I. A near-glacial environment between 13 and 14 kyr B.P. was characterized by poorly ventilated bottom waters followed by a meltwater pulse at circa 13 kyr B.P. During the beginning intrusion of Atlantic Water between 13 and 10 kyr B.P., the bottom water was characterized by somewhat fluctuating temperatures and salinities. Temperatures close to those of the present were established around 9.7 kyr B.P. and seem to have been rather stable since.

Stable isotope geochemistry of pore waters and marine sediments from the New Jersey shelf: Methane formation and fluid origin

Interstitial water and sediment samples of the Integrated Ocean Drilling Program (IODP) expedition 313 "New Jersey Shallow Shelf" were analyzed for chemical composition and stable isotope ratios. A total of 222 water samples were collected from the cores by Rhizon samplers and squeezing of fresh core material. Water was analyzed for its stable oxygen and hydrogen isotope geochemistry (d2H and d18O) at sites M0027A and M0029A, and the carbon isotope composition of the dissolved inorganic carbon (d13CDIC) (all sites). In addition, organic material (Corg) and inorganic carbonates from sediments were analyzed for their carbon ratios (d13Corg and d13Ccarb), and in case of the carbonates also for oxygen (d18Ocarb). Carbon isotopes were also analyzed in samples containing enough methane gas (d13Cmeth). Pore fluids from site M0027A were analyzed for the sulfur isotope composition of dissolved sulfate (d34S). The combination of isotope analyses of all phases (interstitial water, sediment, and gas) with pore water chemistry is expected to enable a better understanding of processes in the sediment and will help to identify the origin of fluids under the New Jersey shelf.

Density, d18O and accumulation rates from snow pits on the Filchner-Ronne Ice Shelf

Accumulation rates in the eastern part of Ronne Ice Shelf were determined by isotopic stratigraphy (18O). The samples were taken from snow-pits dug during the Filchner I and II operations in 1984 and 1986. In general, the accumulation rate decreases towards the south; the greatest decrease, from 21.3 to 13.3 g/cm**2/a, was observed between Filchner Station and measuring point 341, sited 270 km up-stream of the ice edge. The d18O values of the near-surface layers vary between -25 and -29 per mil. The 18O content in the more southerly part is progressively depleted in the direction of Möllereisstrom, paralleling a decrease in the accumulation rate. Near the ice edge the 18O content decreases to the west. A 100 m ice core drilled in 1984 at point 340, 22 km from the ice edge, probably goes back to A.D. 1460; it has been dated by isotopic stratigraphy. The accumulation rate up-stream of the drilling site was deduced from the sequence of annual layers, using a simple ice-flow model. The accumulation shows strong variations over the last 200 years, which may be caused in part by local variations in the accumulation on Ronne Ice shelf.

Seawater carbonate chemistry and nutrients measured on water bottle samples during the International Siberian Shelf Study 2008 (ISSS-08) in the Laptev, East Siberian and Chukchi Seas

The motivation for ISSS-08 was to alleviate the scarcity of observational data on transport and processing of water, sediment and carbon on the East Siberian Arctic Shelves (ESAS). The region is of particular interest from the perspective of carbon-climate couplings as it has witnessed a 4°C springtime positive temperature anomaly for 2000-2005 compared with preceding decades. A complex sampling program was accomplished during the 50-days ISSS-08 cruise August - September 2008 by participants from 12 organizations in Russia, Sweden, UK and USA.

(Table 1) Composition of bottom sediments and pore waters from the West Africa shelf

Organic and mineral phosphorus (P_org and P_min) have been determined in pore waters of terrigenous, biogenous, as well as weakly phosphatic and phosphatic sediments from the shelf of the West Africa (in 30 samples). Concentrations of P_min in the pore waters have been examined in close relation to grain size and chemical composition (amounts of P and N_org) of solid phase of the sediments. It has been demonstrated that among sands and coarse silts, maximum concentrations of P_min (up to 1.7 mg/l) in the pore waters have been observed in weakly phosphatic and phosphatic sediments rich in organic matter of the highly productive shelf of the Southwest Africa. Concentrations of P_min in the pore waters are most clearly associated with contents of N_org in the solid phase of the sediments (correlation coefficient R = 0.71) and P_org in the pore waters (R = 0.78).