92 resultados para LUMINESCENCE SPECTRA

em Publishing Network for Geoscientific


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The Arkhangelsk area lies in the region that was reached by the northeastern flank of the Scandinavian ice sheet during the last glaciation. Investigations of Late Pleistocene sediments show interglacial terrestrial and marine conditions with sea level up to 52 m above the present level. An unconformity in the stratigraphy suggests a hiatus representing the Early Valdaian (Weichselian) and the beginning of the Middle Valdaian. This unconformity could be related to a low base level and isostatic depression of the area north of Arkhangelsk, either caused by ice masses advancing from the Kara and Barents ice sheets and/or to Scandinavian ice over the Kola Peninsula. During Middle Valdaian, from c. 66 ka BP, until the advance of the Late Valdaian glacier, c. 17-16 ka BP, peat formation, and northward fluvial sedimentation occurred coexisting with permafrost conditions in a later phase. Before the glacier advance, the base level rose and thick vertical accumulations of fluvial sediments were formed. Associated with this glacier advance from the north-northwest, ice damming occurred. Fluvial drainage was opposite to the present drainage pattern and deposition appeared in glaciolacustrine ponds in the area outside the limit of the glaciation. After the deglaciation that started c. 15 ka BP, permafrost conditions and downwasting of buried stagnant glacier ice prevailed until at least 10.7 ka BP.

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Some samples from DSDP Holes 530A and 532 were analyzed for their fossil pollen content. The sites are located in the southeastern corner of the Angola Basin, about 200 km west of the present coastline. Fossil pollen assemblages of Holocene to Miocene age were compared with present-day pollen deposition in the arid Namib sand sea. The strong resemblance of all the pollen spectra indicates that very arid conditions existed in the coastal region of Namibia in Quaternary and Pliocene times. These data are in agreement with the late Miocene origin of the coastal aridity and with the conception that upwelling of cold water was responsible for these desert conditions.

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This data set contains 1851 infrared (IR) spectra, forming a single IR map of diamond sample JH7b. This data set is used to show the application of DiaMap, a computer routine written using PERL, to automatically process diamond IR spectra to obtain quantitative impurity data from them. Full abstract will be added after acceptance of publication.

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The large discrepancy between field and laboratory measurements of mineral reaction rates is a long-standing problem in earth sciences, often attributed to factors extrinsic to the mineral itself. Nevertheless, differences in reaction rate are also observed within laboratory measurements, raising the possibility of intrinsic variations as well. Critical insight is available from analysis of the relationship between the reaction rate and its distribution over the mineral surface. This analysis recognizes the fundamental variance of the rate. The resulting anisotropic rate distributions are completely obscured by the common practice of surface area normalization. In a simple experiment using a single crystal and its polycrystalline counterpart, we demonstrate the sensitivity of dissolution rate to grain size, results that undermine the use of "classical" rate constants. Comparison of selected published crystal surface step retreat velocities (Jordan and Rammensee, 1998) as well as large single crystal dissolution data (Busenberg and Plummer, 1986) provide further evidence of this fundamental variability. Our key finding highlights the unsubstantiated use of a single-valued "mean" rate or rate constant as a function of environmental conditions. Reactivity predictions and long-term reservoir stability calculations based on laboratory measurements are thus not directly applicable to natural settings without a probabilistic approach. Such a probabilistic approach must incorporate both the variation of surface energy as a general range (intrinsic variation) as well as constraints to this variation owing to the heterogeneity of complex material (e.g., density of domain borders). We suggest the introduction of surface energy spectra (or the resulting rate spectra) containing information about the probability of existing rate ranges and the critical modes of surface energy.