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21.
Sedimentation in fluvial and lacustrine environments 总被引:1,自引:1,他引:0
Sedimentation in rivers is dominated by a complex set of physical processes, associated with the unidirectional flow of water.
Variations in these processes give rise to different fluvial channel types, whose character can commonly be recognised in
the ancient record. Chemical and biological processes are comparatively unimportant in fluvial sedimentation.
In contrast, physical, chemical or biological processes can each dominate sedimentation in lakes. Physical (clastic) deposition
dominates in high-latitude and mountain lakes (in which chemical and biological activity are low), and in lakes with high
relief of the drainage basin and lake floor. Its variety reflects a range of processes influenced by river inflow, wave and
current action, thermal and density effects.
Economic benefits from the study of lake and river sedimentation include both resource and environmental aspects. An example
is given of a mercury pollution study in a fluvial ecosystem. It shows that return to background levels can take place within
a relatively short interval after cessation of pollutant input. 相似文献
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Olivia Sackett Katherina Petrou Brian Reedy Ross Hill Martina Doblin John Beardall Peter Ralph Philip Heraud 《The ISME journal》2016,10(2):416-426
Diatoms, an important group of phytoplankton, bloom annually in the Southern Ocean, covering thousands of square kilometers and dominating the region''s phytoplankton communities. In their role as the major food source to marine grazers, diatoms supply carbon, nutrients and energy to the Southern Ocean food web. Prevailing environmental conditions influence diatom phenotypic traits (for example, photophysiology, macromolecular composition and morphology), which in turn affect the transfer of energy, carbon and nutrients to grazers and higher trophic levels, as well as oceanic biogeochemical cycles. The paucity of phenotypic data on Southern Ocean phytoplankton limits our understanding of the ecosystem and how it may respond to future environmental change. Here we used a novel approach to create a ‘snapshot'' of cell phenotype. Using mass spectrometry, we measured nitrogen (a proxy for protein), total carbon and carbon-13 enrichment (carbon productivity), then used this data to build spectroscopy-based predictive models. The models were used to provide phenotypic data for samples from a third sample set. Importantly, this approach enabled the first ever rate determination of carbon productivity from a single time point, circumventing the need for time-series measurements. This study showed that Chaetoceros simplex was less productive and had lower protein and carbon content during short-term periods of high salinity. Applying this new phenomics approach to natural phytoplankton samples could provide valuable insight into understanding phytoplankton productivity and function in the marine system. 相似文献
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G A Dunaway G L Leung J R Thrasher M D Cooper 《The Journal of biological chemistry》1978,253(20):7460-7463
Earlier work demonstrated that the activity of liver phosphofructokinase (PFK-L2) and immunoreactive PFK-L2 were decreased in diabetic rats and increased to normal or super-normal amounts following insulin treatment (Dunaway, G.A., and Weber, G., (1974) Arch. Biochem. Biophys. 162, 629-637). This report indicates that the decrease in levels of PFK-L2 in diabetic rats is a result of an accelerated degradation rate while the synthetic rate remains nearly normal. Following insulin treatment, the rate of PFK-L2 synthesis is enhanced 2-fold, whereas the rate of degradation appears to be greatly diminished. An inverse relationship is shown to exist between the PFK-L2 levels and the rates of PFK-L2 degradation, suggesting that the levels of PFK-L2 are primarily regulated by degradation rate. In addition, the levels of the PFK-L2 peptide stabilizing factor are inversely proportional to rates of PFK-L2 degradation. These results indicate that insulin mediates the rate of degradation of PFK-L2 by controlling the level of the peptide stabilizing factor. 相似文献
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Brian A. O'Connell 《BMJ (Clinical research ed.)》1954,2(4898):1206-1208
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