963 resultados para Reversals: Process, Time Scale, Magnetostratigraphy


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This paper contains magnetobiostratigraphic correlation charts for each of the four sites occupied during DSDP Leg 72. Microfossil zonal boundaries and magnetic polarity determinations for Sites 515 through 518 are summarized in Figures 1 through 4, respectively. Our discussion focuses on the correlations derived for the Paleogene and late Cretaceous (Coniacian-Maestrichtian) of Site 516, because of the value of this site as a stratigraphic reference section for the South Atlantic.

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This paper analyzes the correlation between the fluctuations of the electrical power generated by the ensemble of 70 DC/AC inverters from a 45.6 MW PV plant. The use of real electrical power time series from a large collection of photovoltaic inverters of a same plant is an impor- tant contribution in the context of models built upon simplified assumptions to overcome the absence of such data. This data set is divided into three different fluctuation categories with a clustering proce- dure which performs correctly with the clearness index and the wavelet variances. Afterwards, the time dependent correlation between the electrical power time series of the inverters is esti- mated with the wavelet transform. The wavelet correlation depends on the distance between the inverters, the wavelet time scales and the daily fluctuation level. Correlation values for time scales below one minute are low without dependence on the daily fluctuation level. For time scales above 20 minutes, positive high correlation values are obtained, and the decay rate with the distance depends on the daily fluctuation level. At intermediate time scales the correlation depends strongly on the daily fluctuation level. The proposed methods have been implemented using free software. Source code is available as supplementary material.

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Protein folding occurs on a time scale ranging from milliseconds to minutes for a majority of proteins. Computer simulation of protein folding, from a random configuration to the native structure, is nontrivial owing to the large disparity between the simulation and folding time scales. As an effort to overcome this limitation, simple models with idealized protein subdomains, e.g., the diffusion–collision model of Karplus and Weaver, have gained some popularity. We present here new results for the folding of a four-helix bundle within the framework of the diffusion–collision model. Even with such simplifying assumptions, a direct application of standard Brownian dynamics methods would consume 10,000 processor-years on current supercomputers. We circumvent this difficulty by invoking a special Brownian dynamics simulation. The method features the calculation of the mean passage time of an event from the flux overpopulation method and the sampling of events that lead to productive collisions even if their probability is extremely small (because of large free-energy barriers that separate them from the higher probability events). Using these developments, we demonstrate that a coarse-grained model of the four-helix bundle can be simulated in several days on current supercomputers. Furthermore, such simulations yield folding times that are in the range of time scales observed in experiments.

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In this paper, we demonstrate an approach by which some evoked neuronal events can be probed by functional MRI (fMRI) signal with temporal resolution at the time scale of tens of milliseconds. The approach is based on the close relationship between neuronal electrical events and fMRI signal that is experimentally demonstrated in concurrent fMRI and electroencephalographic (EEG) studies conducted in a rat model with forepaw electrical stimulation. We observed a refractory period of neuronal origin in a two-stimuli paradigm: the first stimulation pulse suppressed the evoked activity in both EEG and fMRI signal responding to the subsequent stimulus for a period of several hundred milliseconds. When there was an apparent site–site interaction detected in the evoked EEG signal induced by two stimuli that were primarily targeted to activate two different sites in the brain, fMRI also displayed signal amplitude modulation because of the interactive event. With visual stimulation using two short pulses in the human brain, a similar refractory phenomenon was observed in activated fMRI signals in the primary visual cortex. In addition, for interstimulus intervals shorter than the known latency time of the evoked potential induced by the first stimulus (≈100 ms) in the primary visual cortex of the human brain, the suppression was not present. Thus, by controlling the temporal relation of input tasks, it is possible to study temporal evolution of certain neural events at the time scale of their evoked electrical activity by noninvasive fMRI methodology.

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The astronomical-tuned time scale is rapidly extended into the Paleogene but, due to the existence of an Eocene gap, different tuning options had to be presented for the Paleocene. These options differ both in number and tuning of ~405-kyr eccentricity related cycles and are only partially consistent with recalculated 40Ar/39Ar constraints for the Cretaceous/Paleogene (K/Pg) and Paleocene/Eocene (P/E) boundaries. In this paper, we evaluate the cyclostratigraphic interpretation of records from ODP Leg 198 and 208 sites, and the Zumaia section to solve the problem of the different tuning options. We found that the interval between the K/Pg boundary and the early Late Paleocene biotic event (ELPE) comprises 17 instead of 16 * ~405-kyr eccentricity related cycles as previously proposed, while the entire Paleocene contains 25 * ~405-kyr cycles. Starting from 40Ar/39Ar age constraints for the K/Pg boundary, a new tuning to 405-kyr eccentricity is presented for the Paleocene and earliest Eocene, which results in ages of ~66.0 and ~ 56.0 Ma for the K/Pg and P/E boundaries, respectively. This tuning introduces considerable differences in age for a number of nannofossil events at ODP Sites 1209 and 1262 in the interval between 61 and 63 Ma, but eliminates large and abrupt changes in the seafloor spreading rate. The tuning seems further consistent with recalculated 40Ar/39Ar ages for ash layer -17 of early Eocene age. However, despite this apparent consistency with existing radio-isotopic constraints, an alternative 405-kyr younger or, less likely, older tuning cannot be excluded at this stage.