Fossil record of Mollusca from Neogene sediments in Schleswig-Holstein, Germany

Über die Verbreitung, Gliederung und Ausbildung des Jungtertiärs im westlichen Schleswig-Holstein war bisher nicht viel bekannt. Am besten bearbeitet sind die glazial gestauchten Schollen von Morsum/Sylt. Eine Aufzählung erbohrter Miozänvorkommen mit nicht immer überzeugender Begründung lieferte H.-L. HECK 1935. S. THIELE (1941) hat die ihm bekannten Vorkommen hauptsächlich nach faziellen und petrographischen Gesichtspunkten bearbeitet. Er erkannte richtig die Stellung der Braunkohlensande. Die angekündigte palaeontologische Bearbeitung ist nicht erschienen. Eine allgemeine Übersicht über die Entwicklung des Jungtertiärs bringen W. WOLFE und H.-L. HECK 1949. W. HINSCH lieferte wertvolle Beiträge zur Molluskenfauna und zur Gliederung des Miozäns (1952, 1955). Über neue Vorkommen von Braunkohlen-Sanden berichtete E. DITTMER(1 956), eine erste Übersicht über neue Vorkommen der Hemmoorer Stufe gab derselbe Verfasser 1957.

Miocene molluscan biostratigraphy in Schleswig-Holstein, north Germany

Vierlandian, Behrendorfian (Lower Hemmoorian), Oxlundian (Upper Hemmoorian), Lower and Upper Reinbekian, Langenfeldian and Gramian stages could be proved by evaluation of marine molluscan faunas. The diachrone base of 'Braunkohlensande' is demonstrated by underlying Vierlandian mica clay in the E, and by Hemmoorian substages more to the W, at last the fluviatile facies is replaced completely by euhaline to brachyhaline sandy to silty sediments. Brachyhaline effects in adjacent environments make possible an approximate dating on fluviatile sedimentation. The widest extension of 'Braunkohlensand' is during upper Oxlundian, whilst slightly brachyhaline Katzheide beds, defined in this paper to be of Lower Reinbekian age, indicate a limit of 'Braunkohlensande' more to the E. Winnert-fauna was found to be a mixture of Oxlundian and Langenfeldian; the overlying lignitic sands belong to the Kaolinsand group. Upper mica clay overlying Miocene Braunkohlensande can be divided into beds of Upper Reinbekian, Langenfeldian and Gramian ages.

Abundance and biomass of planktonic diatom Proboscia alata and associated species, chlorophyll a, organic carbon and nitrogen concentrations in waters over the Bering Sea middle shelf in August 2001

During most of the vegetation season from late May to early September large-sized diatom alga Proboscia alata forms local patches with high abundances and biomasses in different oceanographic domains of the eastern Bering Sea shelf. For 0-25 m layer average abundance and biomass of species in these patches are 700000 cells/l and 5 g/m**3 (wet weight), while corresponding estimates for the layer of maximal species concentrations are 40000000 cells/l and 38 g/m**3 (wet weight) or 1.6 g C/m**3. These levels of abundance and biomass are typical for the spring diatom bloom in the region. Outbursts of P. alata mass development are important for the carbon cycle in the pelagic zone of the shelf area in the summer season. The paradox of P. alata summertime blooms over the middle shelf lies in their occurrences against the background of the sharp seasonal pycnocline and deficiency in nutrients in the upper mixed layer. Duration of the outbursts in P. alata development is about two weeks and size of patches with high abundances can be as large as 200 km across. Degradation of the P. alata summertime outbursts may occur during 4-5 days. Rapid sinking of cells through the seasonal pycnocline results in intense transport of organic matter to bottom sediments. One of possible factors responsible for rapid degradation of the blooms is affect on the population by ectoparasitic flagellates. At terminal stages of the P. alata blooms percentage of infected cells can reach 70-99%.

Seawater carbonate chemistry, nutrients, chlorophyll and diatom Proboscia alata during experiments, 2012

The combined effects of different light and aqueous CO2 conditions were assessed for the Southern Ocean diatom Proboscia alata(Brightwell) Sundström in laboratory experiments. Selected culture conditions (light and CO2(aq)) were representative for the natural ranges in the modern Southern Ocean. Light conditions were 40 (low) and 240 (high) µmol photons/m**2/s. The three CO2(aq) conditions ranged from 8 to 34 µmol/kg CO2(aq) (equivalent to a pCO2 from 137 to 598 µatm, respectively). Clear morphological changes were induced by these different CO2(aq) conditions. Cells in low [CO2(aq)] formed spirals, while many cells in high [CO2(aq)] disintegrated. Cell size and volume were significantly affected by the different CO2(aq) concentrations. Increasing CO2(aq) concentrations led to an increase in particulate organic carbon concentrations per cell in the high light cultures, with exactly the opposite happening in the low light cultures. However, other parameters measured were not influenced by the range of CO2(aq) treatments. This included growth rates, chlorophyll aconcentration and photosynthetic yield (FV/FM). Different light treatments had a large effect on nutrient uptake. High light conditions caused an increased nutrient uptake rate compared to cells grown in low light conditions. Light and CO2 conditions co-determined in various ways the response of P. alata to changing environmental conditions. Overall P. alata appeared to be well adapted to the natural variability in light availability and CO2(aq) concentration of the modern Southern Ocean. Nevertheless, our results showed that P. alata is susceptible to future changes in inorganic carbon concentrations in the Southern Ocean.