22 resultados para Conversion of Citral
Resumo:
The quantitative diatom analysis of 218 surface sediment samples recovered in the Atlantic and western Indian sector of the Southern Ocean is used to define a base of reference data for paleotemperature estimations from diatom assemblages using the Imbrie and Kipp transfer function method. The criteria which justify the exclusion of samples and species out of the raw data set in order to define a reference database are outlined and discussed. Sensitivity tests with eight data sets were achieved evaluating the effects of overall dominance of single species, different methods of species abundance ranking, and no-analog conditions (e.g., Eucampia Antarctica) on the estimated paleotemperatures. The defined transfer functions were applied on a sediment core from the northern Antarctic zone. Overall dominance of Fragilariopsis kerguelensis in the diatom assemblages resulted in a close affinity between paleotemperature curve and relative abundance pattern of this species downcore. Logarithmic conversion of counting data applied with other ranking methods in order to compensate the dominance of F. kerguelensis revealed the best statistical results. A reliable diatom transfer function for future paleotemperature estimations is presented.
Resumo:
Cretaceous chert and porcellanite recovered at Site 436, east of northern Honshu, Japan, are texturally and mineralogically similar to siliceous rocks of comparable age at Sites 303, 304, and 307 in the northwest Pacific. These rocks probably were formed by impregnation of the associated pelagic clay with locally derived silica from biogenic and perhaps some volcanic debris. Fine horizontal laminations are the only primary sedimentary structures, suggesting minimal reworking and transport. Collapse breccias and incipient chert nodules are diagenetic features related to silicification and compaction of the original sediment. Disordered opal-CT (d[101] = 4.09 Å) and microgranular quartz (crystallinity index < 1.0) are the two common silica minerals present. Some samples show quartz replacing this poorly ordered opal- CT, supporting the notion that opal-CT does not become completely ordered (i.e., d[101] = 4.04 Å) in some cases before being converted to quartz. The present temperature calculated for the depth of the shallowest chert and porcellanite at this site is 30 °C; this may represent the temperature of conversion of opal-CT to quartz. High reflection coefficients (0.29-0.65) calculated for the boundary between chert-porcellanite and clay-claystone support the common observation that chert is a strong seismic reflector in deep-sea sedimentary sections.
Resumo:
Phosphorus is an essential nutrient for life. In the ocean, phosphorus burial regulates marine primary production**1, 2. Phosphorus is removed from the ocean by sedimentation of organic matter, and the subsequent conversion of organic phosphorus to phosphate minerals such as apatite, and ultimately phosphorite deposits**3, 4. Bacteria are thought to mediate these processes**5, but the mechanism of sequestration has remained unclear. Here, we present results from laboratory incubations in which we labelled organic-rich sediments from the Benguela upwelling system, Namibia, with a 33P-radiotracer, and tracked the fate of the phosphorus. We show that under both anoxic and oxic conditions, large sulphide-oxidizing bacteria accumulate 33P in their cells, and catalyse the nearly instantaneous conversion of phosphate to apatite. Apatite formation was greatest under anoxic conditions. Nutrient analyses of Namibian upwelling waters and sediments suggest that the rate of phosphate-to-apatite conversion beneath anoxic bottom waters exceeds the rate of phosphorus release during organic matter mineralization in the upper sediment layers. We suggest that bacterial apatite formation is a significant phosphorus sink under anoxic bottom-water conditions. Expanding oxygen minimum zones are projected in simulations of future climate change**6, potentially increasing sequestration of marine phosphate, and restricting marine productivity.
Resumo:
Stable isotopic analyses of Middle Miocene to Quaternary foraminiferal calcite from east equatorial and central north Pacific DSDP cores have provided much new informatlon on the paleoceanography of the Pacific Neogene The history of delta18O change in planktonic foraminifera reflects the changing Isotopic composition and temperature of seawater at the time of test formation. Changes in the isotopic composition of benthonic foraminifera largely reflect changes m the volume of continental ice. Isotopic data from these cores indicates the following sequence of events related to continental glaciation (1) A permanent Antarctic ice sheet developed late in the Middle Miocene (about 13 to 11.5 m.y. ago) (2) The Late Miocene (about 11.5 to 5 m.y. ago) is marked by significant variation in delta18O of about 0.5? throughout, indicating instability of Antarctic ice cap size or bottom-water temperatures (3) The early Pliocene (5 to about 3 m.y. ago) was a time of relative stability in ice volume and bottom-water temperature (4) Growth of permanent Northern Hemisphere ice sheets is referred to have begun about 3 m.y. ago (5) The late Pliocene (3 to about 1.8 m.y. ago) is marked by one major glaciation or bottom-water cooling dated between about 2.1 to 2.3 m.y. (6) There is some evidence that the frequency of glacial-interglacial cycles increased at about 0.9 m.y. There is significant variation in delta13C at these sites but no geochemical interpretation is offered in this paper. The most outstanding feature of delta13C results is a permanent shift of about -0.8? found at about 6.5 m.y. in east equatorial and central north Pacific benthonic foraminifera. This benthonic carbon shift may form a useful marker in deep-sea cores recovering Late Miocene carbonates.