990 resultados para Breitgrund Channel, Kiel Bay


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Sea level related radiocarbon, palynological and stratigraphical data from sediment cores in the Western Baltic have been tested against the existing sea level curves for the region. The relative sea level rise curves for the beginning of the Holocene show no significant deviations between the Kiel, Mecklenburg und Lübeck Bays and hence do not support the previously reported differences in the averaged regional subsidence rates for this time interval. Local subsidence and upheaval due to salt tectonics probably played a greater role than previously suspected in the region. The sea level possibly stagnated around -28 m during the early Holocene before rising very rapidly to -14 m. The submarine terraces at -30 m and perhaps also at -27 m were formed during the lacustrine phase of the Western Baltic when the water levels were controlled by the main thresholds in the Great Belt.

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Various types of trace fossils have been studied on radiographs of sediment cores from the Western Baltic since the early nineteen sixties. lnvestigations on the endo- und epifauna including their habitats and population densities carried out independently by biologists helped to identify the processes of their formation and classify the structures. Biogenic traces are ubiquitous in both sandy and muddy sediments of the Great Belt, where the bottom waters are weil oxygenated through inflows from the North Sea (through Kattegat-Skagerrak). Almost all types of bioturbation structures encountered in the Kiel Bay are also observed in a variety of shapes and forms, and can be considered as representative for the Western Baltic area. Polychaetes, bivalves and echinoderms were recorded at the sediment surface of the cores, and also in living positions in the sediment. The different types of burrows having distint outlines ('trace fossis'), and those having indistinct outlines ('biodeformational strctures'), and their varying abundance encountered in the area have been linked, wherever possible, to the sediment type, and to the macro-benthos.

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The marine transgression Into the Baltic Sea through the Great Belt took place around 9,370 calibrated C-14-years B.P. The sedimentary sequence from the early brackish phase and the change to marine conditions has been investigated in detail through C-14-datings, and oxygen and carbon isotope measurements, and is interpreted by comparison with modern analogs. The oldest brackish sediments are the strongly laminated clays and silts rich in organic carbon followed by non-laminated heavily bioturbated silts. The bedding and textural characteristics and stable isotope analyses on Ammonia beccarii (dextral) and A. beccarii (sinistral) show that the deposltlonal conditions respond to a change at about 9,100 cal. a B.P. from an unstratified brackish water environment in the initial stage of the Littorina Transgression to a thermohaline layered milieu in the upper unit. The oxygen isotope results indicate that the bottom waters of this latter period had salinities and temperatures comparable to the present day Kiel Bay waters. The isotopic composition of the total organic carbon and the d13C-values of A. beccarii reveal a gradual change from an initially lacustrine/terrestrial provenance toward a brackish/marine dominated depositional environment. A stagnation of the sea level at around 9,100 to 9,400 B.P. is indicated.

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The L type calcium channel agonist (±)Bay K 8644 has been reported to cause characteristic motor abnormalities in adult mice. The current study shows that administration of this drug can also cause the unusual phenomenon of self-injurious biting, particularly when given to young mice. Self-biting is provoked by injecting small quantities of (±)Bay K 8644 directly into the lateral ventricle of the brain, suggesting a central effect of the drug. Similar behaviors can be provoked by administration of another L type calcium channel agonist, FPL 64176. The self-biting provoked by (±)Bay K 8644 can be inhibited by pretreating the mice with dihydropyridine L type calcium channel antagonists such as nifedipine, nimodipine, or nitrendipine. However, self-biting is not inhibited by nondihydropyridine antagonists including diltiazem, flunarizine, or verapamil. The known actions of (±)Bay K 8644 as an L type calcium channel agonist, the reproduction of similar behavior with another L type calcium channel agonist, and the protection afforded by certain L type calcium channel antagonists implicate calcium channels in the mediation of the self-biting behavior. This phenomenon provides a model for studying the neurobiology of this unusual behavior.

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We used modern epibenthic foraminifer tests of Cibicidoides mundulus and Planulina wuellerstorfi from South Atlantic core top sediments in order to establish Mg/Ca-temperature relationships for the temperature range from 0 to 15°C. We obtained the following calibrations: Mg/Ca (mmol/mol) = 0.830*exp(0.145*BWT (°C)) for P. wuellerstorfi, and Mg/Ca (mmol/mol) = 0.627*exp(0.143*BWT (°C)) for C. mundulus. However, a number of tests, especially those bathed in North Atlantic Deep Water, revealed higher Mg/Ca ratios than predicted from the calibration. Our data suggest that d[CO3 2-] of bottom water exerts a significant control on dMg/Ca (temperature-corrected) of C. mundulus (dMg/Ca = 0.017*d[CO3 2-] -0.14), while dMg/Ca of P. wuellerstorfi is more likely to be governed by TCO2 (dMg/Ca = -0.007*TCO2 + 15). Since both d[CO3 2-] and TCO2 are closely linked to [CO3 2-], it is inferred that carbonate ion acts as secondary control, after temperature, on benthic shell Mg/Ca below -4°C. A drop in [CO3 2-] by 25 ?mol/kg at 4 km water depth, as suggested for the Last Glacial Maximum, would decrease Mg/Ca by up to 0.4 mmol/mol, which leads to an underestimation of bottom water temperature by -3.5°C. Therefore our results indicate that the Mg/Ca thermometer should be used cautiously for benthic foraminifers where changes in the carbonate chemistry are present in the paleoceanographic record.

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Quantitative proofs for the occurrence of juvenile cods in the Bornholm Sea, which had been spawned in Kiel Bay or Mecklenburg Bay, were the staring point to develop a method, which makes quantitative estimates possible. From these analyses it could be estimated that 20 to 50 % of the cods in the area of the eastern Baltic stock had been spawned in the western Baltic Sea. This expansion in eastern direction was determined partly by passive transport of pelagic cod stages. The main factor was an active migration of cod in the first year of their life. These analyses suggest the necessity to reassess the actual model of the relations between the Baltic cod stocks.

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Analyses of the previous years showed that the reproduction of the Belt Sea cod stock (Gadus morhua morhua) is also very important for the cod stock of the central Baltic Sea (Gadus morhua calarias). Oeberst (1999, 2000) proved, that between 20 % and 50 % of the cods caught in the Bornholm Sea at the age of 2 or 3 years between 1994 and 1998, were spawned in the Belt Sea. On account of this large significance of the Belt Sea cod stock, information regarding the reproduction process are important. The goal of the article presented is the description of the actual spawning areas of the Belt Sea cod stock by means of the spatial distribution of the spawners based on characteristic parameters as the maturity stages and the proportion of the sexes. The basis for these analyses are data sampled between 1992 and 1999. The analyses showed that the actual main spawning areas in the western Baltic Sea were the deeper regions of the Kiel Bay, of the Fehmarn Bay and of the western Mecklenburg Bay. In these regions spawning cods were regularly observed with high intensity. Furthermore, the deeper basin of the Arkona Sea is an important spawning area.

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Investigations concerning the intensity and duration of spawning seasons of cod stocks are parts of the work of the reproductions ecology of commercial fish stocks in the Baltic Sea. The Institute of Baltic Fisheries Rostock has sampled and analysed data for this goal since 1992. The first data analyses for the spawning season 1997, sampled in the areas Kiel Bay, Mecklenburg Bay and Arkona Sea showed that the process of the spawning season is different compared to the years before. The spawning process starts earlier than the other years in Kiel Bay and Mecklenburg Bay. The results show that a high proportion of the spawning stock was part of the spawning process in this area. The Arkona Sea cod are regarded by ICES definition as belonging to the western cod stock. In this ICES sub-division only a low number of spawned cod was observed in March, the main spawning time of the western cod stock. Opposite to the theory of the stock units intensive spawning activities were observed in June as in the years before in the Arkona Sea.