Water chemistry and fluffy layer geochemistry and mineral content at four sites in the western Baltic Sea

The fluffy layer was sampled repeatedly during nine expeditions between October 1996 and December 1998 at four stations situated along a S-N-transect from the Oder Estuary to the Arkona Basin. Geochemical and mineralogical analyses of the fluff show regional differences (trends) in composition, attributed to provenance and to hydrographical conditions along their transport pathways. Temporal variability is very high at the shallow water station of the estuary, and decreases towards the deeper stations in the north. In the shallow water area, intensive resuspension of the fluff due to wind-driven waves and currents leads to an average residence time of only one to two days. Near-bottom lateral transport of the fluff is the main process that transfers the fine grained material, containing both nutrients and contaminants, from the coastal zone into the deeper basins of the Baltic Sea. Seasonal effects (e.g. biogenic production in relation to trace metal variation) are observed at the Tromper Wiek station, where the residence time of the fluffy material is in the scale of seasons. Thus, the fluffy layer offers suitable material for environmental monitoring programs.

(Table 2) Chemical composition of phosphates from the Namibian and Chilean shelves

This study on phosphorites of different compositions and ages from shelf sediments and seamounts of the Pacific Ocean by means of analytical electron microscopy showed that these phosphorites contain ultra-microscopic inclusions of authigenic minerals and, more rarely, of rare earth element (REE) minerals. In some of phosphorite samples of Pleistocene-Pliocene age from the Namibian shelf both kinds of minerals were found. Uranium minerals were represented by uraninite, coffinite, and ningioite; those of REE - by monazite, xenotime, and bastnesite, which points to their potential accumulation not only as isomorphous admixtures in calcium phosphate but also as independent mineral phases. Coexistence of the minerals noted in shelf phosphorites is caused by repeated changes in redox conditions during formation and then redeposition of phosphate concretions. Presence of uranium minerals in phosphorites from seamounts shows that during an initial step of formation of these phosphorites environment was rather suboxic or reductive than oxic.