(Table 1) Composition of manganese-iron accumulates in the Kiel Bay, western Baltic Sea

Manganese-iron accumulates in the Kiel Bay were investigated with regard to their occurence, chemical composition and formation. Three morphologically different types were identified: a) growth on mussels, b) spherical nodules (ca. 1-3 cm) and c) disshaped symetrical and asymetrical nodules (up to 10 cm). Average values from 110 accumulates representing the three types were: Mn 29.3%, Fe 10.0%, Co 77 ppm, Ni 97 ppm, Cu 21 ppm and Zn 340 ppm. Accumulates on mussels showed the highest trace metal concentrations. A growth rate of ca. 0.6 mm/yr for type (a) was estimated. Heavy metal concentrations were determined in ca. 60 sediment and 30 pore water samples, and in 110 Baltic sea water samples. During certain periods, large increases in Mn values (up to 400 (µg/l) were found in the deeper waters. These concentrations develop during periods of strong stagnant conditions in the sediments where dissolution of Mn oxides, and diffusion mobilizes the Mn into the overlying waters. The manganese is then reprecipitated close to the boundary of the O2-enriched surface waters. This critical O2-concentration was found to be 40% saturation. In the Kiel Bay, Mn-Fe-accumulates are found in a zone which marks the upper limit sometimes reached by the deep waters of lower O2-concentration. Additionally, the availability of larger particles (especially stones or mussels) on the sediment surface is necessary. These conditions are met in the Kiel Bay in a water depth of 20-28 m at several places.

(Table 1) Time series of ostracod population density off Bokniseck shore ('Hausgarten'), western Baltic Sea

Seasonal distributions of ostracode species from the Bay of Kiel, western Baltic Sea (Bokniseck, 'Hausgarten') were studied at seven observation stations located between 6 - 23.5 m water depth. During the period from December 1973 to March 1975, 175 samples were taken every two weeks from the sediment surface at each station. Environmental factors were measured simultaneously with sampling. Most of the ostracode species were present in all of the samples throughout the year; four species were found to be seasonal. On the other hand, the population densities of each of the examined ostracode species, as revealed by countings, indicate marked seasonal variations. These variations are attributed to changes in length rate and timing of the reproductive cycles of the different ostracode species, effected mainly by food supply. Maxima in the abundance of the ostracode species with short (1/2 - 1 month) life cycles, occurred simultaneously with peaks of food supply in spring and autumn, whereas the maxima abundance of ostracodes with longer (10 - 12 months) life cycles was delayed.