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24,520 result(s) for "Frequency spectrum"
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The Interdecadal Shift of ENSO Properties in 1999/2000
Following the interdecadal shift of El Niño–Southern Oscillation (ENSO) properties that occurred in 1976/77, another regime shift happened in 1999/2000 that featured a decrease of variability and an increase in ENSO frequency. Specifically, the frequency spectrum of Niño-3.4 sea surface temperature shifted from dominant variations at quasi-quadrennial (∼4 yr) periods during 1979–99 to weaker fluctuations at quasi-biennial (∼2 yr) periods during 2000–18. Also, the spectrum of warm water volume (WWV) index had almost no peak in 2000–18, implying a nearly white noise process. The regime shift was associated with an enhanced zonal gradient of the mean state, a west ward shift in the atmosphere–ocean coupling in the tropical Pacific, and an increase in the static stability of the troposphere. This shift had several important implications. The whitening of the subsurface ocean temperature led to a breakdown of the relationship between WWV and ENSO, reducing the efficacy of WWV as a key predictor for ENSO and thus leading to a decrease in ENSO prediction skill. Another consequence of the higher ENSO frequency after 1999/2000 was that the forecasted peak of sea surface temperature anomaly often lagged that observed by several months, and the lag increased with the lead time. The ENSO regime shift may have altered ENSO influences on extratropical climate. Thus, the regime shift of ENSO in 1999/2000 as well as the model default may account for the higher false alarm and lower skill in predicting ENSO since 1999/2000.
Inferring the Joint Demographic History of Multiple Populations: Beyond the Diffusion Approximation
Patterns of genetic variation across populations are influenced by mutation, selection, genetic drift, and migrations. Building models of evolution... Understanding variation in allele frequencies across populations is a central goal of population genetics. Classical models for the distribution of allele frequencies, using forward simulation, coalescent theory, or the diffusion approximation, have been applied extensively for demographic inference, medical study design, and evolutionary studies. Here we propose a tractable model of ordinary differential equations for the evolution of allele frequencies that is closely related to the diffusion approximation but avoids many of its limitations and approximations. We show that the approach is typically faster, more numerically stable, and more easily generalizable than the state-of-the-art software implementation of the diffusion approximation. We present a number of applications to human sequence data, including demographic inference with a five-population joint frequency spectrum and a discussion of the robustness of the out-of-Africa model inference to the choice of modern population.
Conditions for validity of mean flow stability analysis
This article provides theoretical conditions for the use and meaning of a stability analysis around a mean flow. As such, it may be considered as an extension of the works by McKeon & Sharma (J. Fluid Mech., vol. 658, 2010, pp. 336–382) to non-parallel flows and by Turton et al. (Phys. Rev. E, vol. 91 (4), 2015, 043009) to broadband flows. Considering a Reynolds decomposition of the flow field, the spectral (or temporal Fourier) mode of the fluctuation field is found to be equal to the action on a turbulent forcing term by the resolvent operator arising from linearisation about the mean flow. The main result of the article states that if, at a particular frequency, the dominant singular value of the resolvent is much larger than all others and if the turbulent forcing at this frequency does not display any preferential direction toward one of the suboptimal forcings, then the spectral mode is directly proportional to the dominant optimal response mode of the resolvent at this frequency. Such conditions are generally met in the case of weakly non-parallel open flows exhibiting a convectively unstable mean flow. The spatial structure of the singular mode may in these cases be approximated by a local spatial stability analysis based on parabolised stability equations (PSE). We have also shown that the frequency spectrum of the flow field at any arbitrary location of the domain may be predicted from the frequency evolution of the dominant optimal response mode and the knowledge of the frequency spectrum at one or more points. Results are illustrated in the case of a high Reynolds number turbulent backward facing step flow.
Observation-Based Source Terms in the Third-Generation Wave Model WAVEWATCH III: Updates and Verification
The observation-based source terms available in the third-generation wave model WAVEWATCH III (i.e., the ST6 package for parameterizations of wind input, wave breaking, and swell dissipation terms) are recalibrated and verified against a series of academic and realistic simulations, including the fetch/duration-limited test, a Lake Michigan hindcast, and a 1-yr global hindcast. The updated ST6 not only performs well in predicting commonly used bulk wave parameters (e.g., significant wave height and wave period) but also yields a clearly improved estimation of high-frequency energy level (in terms of saturation spectrum and mean square slope). In the duration-limited test, we investigate the modeled wave spectrum in a detailed way by introducing spectral metrics for the tail and the peak of the omnidirectional wave spectrum and for the directionality of the two-dimensional frequency–direction spectrum. The omnidirectional frequency spectrum E ( f ) from the recalibrated ST6 shows a clear transition behavior from a power law of approximately f −4 to a power law of about f −5 , comparable to previous field studies. Different solvers for nonlinear wave interactions are applied with ST6, including the Discrete Interaction Approximation (DIA), the more expensive Generalized Multiple DIA (GMD), and the very expensive exact solutions [using the Webb–Resio–Tracy method (WRT)]. The GMD-simulated E ( f ) is in excellent agreement with that from WRT. Nonetheless, we find the peak of E ( f ) modeled by the GMD and WRT appears too narrow. It is also shown that in the 1-yr global hindcast, the DIA-based model overestimates the low-frequency wave energy (wave period T > 16 s) by 90%. Such model errors are reduced significantly by the GMD to ~20%.
Damage Evolution During Rock Dynamic Compression Revealed by Wavelet Analysis of Acoustic Emission Signals
Acoustic emissions have been monitored during rock compression under both quasi-static and dynamic conditions. A new method is proposed in this study to study the damage evolution of rocks during dynamic compression by continuous wavelet analysis of acoustic emission signals. Wavelet analysis is first validated against conventional method using the acoustic emission data from a quasi-static compression test. The wavelet analysis is then carried out on acoustic emission signals from rock dynamic compression to obtain the time–frequency spectrum. Based on the characteristics of the time–frequency spectrums, the rock exhibits a mixed damage mode shifting from tensile to shear damage. The increase in the loading rate leads to an increase in the amount of tensile damage. The proposed method provides an effective way to analyze the dynamic damage evolution of rocks.HighlightsA new method is proposed to study the damage evolution during rock dynamic compression using acoustic emission (AE) signals.This method uses the characteristics of time–frequency spectrum of AE signals obtained from continuous wavelet analysis.During dynamic compression the rock exhibits a mixed damage mode shifting from tensile to shear damage.
A unifying theory of jet screech
This paper describes the mechanism underpinning modal staging behaviour in screeching jets. An upstream-propagating subsonic guided-jet mode is shown to be active in all stages of screech. Axial variation of shock-cell spacing manifests in the spectral domain as a series of suboptimal peaks. It is demonstrated that the guided-jet mode may be energized by interactions of the Kelvin–Helmholtz wavepacket with not only the primary shock wavenumber peak, but also suboptimal peaks; interaction with suboptimals is shown to be responsible for closing the resonance loop in multiple stages of jet screech. A consideration of the full spectral representation of the shocks reconciles several of the classical models and results for jet screech that had heretofore been paradoxical. It is demonstrated that there are multiple standing waves present in the near field of screeching jets, corresponding to the superposition of the various waves active in these jets. Multimodal behaviour is explored for jets in a range of conditions, demonstrating that multiple peaks in the frequency spectra can be due to either changes in which peak of the shock spectra the Kelvin–Helmholtz wavepacket is interacting with, or a change in azimuthal mode, or both. The absence of modal staging in high-aspect-ratio non-axisymmetric jets is also explained in the context of the aforementioned mechanism. The paper closes with a new proposed theory for frequency selection in screeching jets, based on the observation that these triadic interactions appear to underpin selection of the guided-jet mode wavelength in all measured cases.
SweeD: Likelihood-Based Detection of Selective Sweeps in Thousands of Genomes
The advent of modern DNA sequencing technology is the driving force in obtaining complete intra-specific genomes that can be used to detect loci that have been subject to positive selection in the recent past. Based on selective sweep theory, beneficial loci can be detected by examining the single nucleotide polymorphism patterns in intraspecific genome alignments. In the last decade, a plethora of algorithms for identifying selective sweeps have been developed. However, the majority of these algorithms have not been designed for analyzing whole-genome data. We present SweeD (Sweep Detector), an open-source tool for the rapid detection of selective sweeps in whole genomes. It analyzes site frequency spectra and represents a substantial extension of the widely used SweepFinder program. The sequential version of SweeD is up to 22 times faster than SweepFinder and, more importantly, is able to analyze thousands of sequences. We also provide a parallel implementation of SweeD for multi-core processors. Furthermore, we implemented a checkpointing mechanism that allows to deploy SweeD on cluster systems with queue execution time restrictions, as well as to resume long-running analyses after processor failures. In addition, the user can specify various demographic models via the command-line to calculate their theoretically expected site frequency spectra. Therefore, (in contrast to SweepFinder) the neutral site frequencies can optionally be directly calculated from a given demographic model. We show that an increase of sample size results in more precise detection of positive selection. Thus, the ability to analyze substantially larger sample sizes by using SweeD leads to more accurate sweep detection. We validate SweeD via simulations and by scanning the first chromosome from the 1000 human Genomes project for selective sweeps. We compare SweeD results with results from a linkage-disequilibrium-based approach and identify common outliers.
A New Conjugate Gradient Method for Moving Force Identification of Vehicle–Bridge System
A new preconditioned modified conjugate gradient algorithm based on improved gradient operator and preconditioned technology is proposed for moving force identification of bridge structure in this paper. First, the moving load identification problem is converted into the problem of solving large-scale linear equations by the time-domain deconvolution technology and modal superposition method. Then the large-scale linear equations problem is transformed into easily solved equivalent problem by preprocessing. Subsequently, it is transformed into an unconstrained linear optimization problem by constructing the corresponding objective function. Finally, the problem is solved by the proposed conjugate gradient method. The innovation of the proposed method lies in two aspects. First, the proposed conjugate gradient method is proved by mathematical theory. Second, before constructing the objective function, the preconditioned technique is utilized to simplify the original problem. A series of numerical simulations are carried out to verify the stability and effectiveness of the proposed approach under 21 kinds of noise levels and 6 different sensor configurations, and its performances are compared with several conjugate gradient methods. The results show that the proposed method can reduce the iteration number, and also ensure the load identification accuracy, which indicates that the proposed method can improve the speed of identification and effectively reduce the cost. Meanwhile, the identification situation of different load components is studied by the frequency spectrum analysis method. It is found that the proposed method is a stable and a reliable identification method for static and low-frequency components, which provides a new idea for dynamic weighing of low-frequency loads on bridges.
Inference of the Distribution of Selection Coefficients for New Nonsynonymous Mutations Using Large Samples
The distribution of fitness effects (DFE) has considerable importance in population genetics. To date, estimates of the DFE come from studies using a small number of individuals. Thus, estimates of the proportion of moderately to strongly deleterious new mutations may be unreliable because such variants are unlikely to be segregating in the data. Additionally, the true functional form of the DFE is unknown, and estimates of the DFE differ significantly between studies. Here we present a flexible and computationally tractable method, called Fit∂a∂i, to estimate the DFE of new mutations using the site frequency spectrum from a large number of individuals. We apply our approach to the frequency spectrum of 1300 Europeans from the Exome Sequencing Project ESP6400 data set, 1298 Danes from the LuCamp data set, and 432 Europeans from the 1000 Genomes Project to estimate the DFE of deleterious nonsynonymous mutations. We infer significantly fewer (0.38–0.84 fold) strongly deleterious mutations with selection coefficient |s| > 0.01 and more (1.24–1.43 fold) weakly deleterious mutations with selection coefficient |s| < 0.001 compared to previous estimates. Furthermore, a DFE that is a mixture distribution of a point mass at neutrality plus a gamma distribution fits better than a gamma distribution in two of the three data sets. Our results suggest that nearly neutral forces play a larger role in human evolution than previously thought.
Inferring the Probability of the Derived vs. the Ancestral Allelic State at a Polymorphic Site
It is known that the allele ancestral to the variation at a polymorphic site cannot be assigned with certainty, and that the most frequently used method to assign the ancestral state—maximum parsimony—is prone to misinference. Estimates of counts of sites that have a certain number of copies of the derived allele in a sample (the unfolded site frequency spectrum, uSFS) made by parsimony are therefore also biased. We previously developed a maximum likelihood method to estimate the uSFS for a focal species using information from two outgroups while assuming simple models of nucleotide substitution. Here, we extend this approach to allow multiple outgroups (implemented for three outgroups), potentially any phylogenetic tree topology, and more complex models of nucleotide substitution. We find, however, that two outgroups and the Kimura two-parameter model are adequate for uSFS inference in most cases. We show that using parsimony to infer the ancestral state at a specific site seriously breaks down in two situations. The first is where the outgroups provide no information about the ancestral state of variation in the focal species. In this case, nucleotide variation will be underestimated if such sites are excluded. The second is where the minor allele in the focal species agrees with the allelic state of the outgroups. In this situation, parsimony tends to overestimate the probability of the major allele being derived, because it fails to account for the fact that sites with a high frequency of the derived allele tend to be rare. We present a method that corrects this deficiency and is capable of providing nearly unbiased estimates of ancestral state probabilities on a site-by-site basis and the uSFS.