Optimal 3-D traveltime tomography

Geophysics ◽  
1998 ◽  
Vol 63 (3) ◽  
pp. 1053-1061 ◽  
Author(s):  
Margaret J. Eppstein ◽  
David E. Dougherty

We propose a practical new method for 3-D traveltime tomography. The method combines an efficient approximation to the extended Kalman filter for rapid, accurate, nonlinear tomography, with the concept of data‐driven zonation, in which the dimensionality and geometry of the parameterization are dynamically determined using cluster analysis and region merging by random field union. The Bayesian filter uses geostatistics as it recursively incorporates measurements in an optimal (minimum‐variance) manner. Geologic knowledge is introduced through a priori estimates of the parameter field and its spatial covariance. Conditional estimates of the parameter number, geometry, value, and covariance are evolved. An initial decomposition of the 3-D domain into 2-D slices, the simplified filter design, and the data‐driven reduction in parameter dimensionality, all contribute to make the method computationally feasible for large 3-D domains. The method is verified by the inversion of crosswell seismic traveltimes to 3-D estimates of seismic slowness in four synthetic heterogeneous domains. Starting with homogeneous, fully distributed slowness fields, and no knowledge of the true covariance structure, the method is able to accurately and efficiently resolve the structure and values of markedly different domains.

Author(s):  
Bryce A. Roth ◽  
David L. Doel ◽  
Jeffrey J. Cissell

This paper describes the development of an improved method for reliable, repeatable, and accurate matching of engine performance models to test data. The centerpiece of this approach is a minimum variance estimator algorithm with a priori estimates which addresses both deterministic and probabilistic aspects of the problem. Specific probabilistic aspects include uncertainty in the measurements, prior expectations on model matching parameters, and noise in the power setting parameters. The algorithm is able to produce optimal results using any number of measurements and model matching parameters and can therefore take advantage of all measured data to produce the best possible match. This improves on current matching algorithms which require that the number of measured parameters be equal to the number of model matching parameters. This algorithm has been implemented in the Numerical Propulsion System Simulation (NPSS) and tested on a generic high-bypass turbofan model typical of those used in commercial service. The baseline engine model and simulated test data are described in detail. Several exercises are discussed to illustrate results available from this algorithm including the matching of a typical power calibration data set and matching of a typical production engine data set.


2020 ◽  
Vol 57 (1) ◽  
pp. 68-90 ◽  
Author(s):  
Tahir S. Gadjiev ◽  
Vagif S. Guliyev ◽  
Konul G. Suleymanova

Abstract In this paper, we obtain generalized weighted Sobolev-Morrey estimates with weights from the Muckenhoupt class Ap by establishing boundedness of several important operators in harmonic analysis such as Hardy-Littlewood operators and Calderon-Zygmund singular integral operators in generalized weighted Morrey spaces. As a consequence, a priori estimates for the weak solutions Dirichlet boundary problem uniformly elliptic equations of higher order in generalized weighted Sobolev-Morrey spaces in a smooth bounded domain Ω ⊂ ℝn are obtained.


Author(s):  
Giuseppe Maria Coclite ◽  
Lorenzo di Ruvo

The Rosenau-Korteweg-de Vries equation describes the wave-wave and wave-wall interactions. In this paper, we prove that, as the diffusion parameter is near zero, it coincides with the Korteweg-de Vries equation. The proof relies on deriving suitable a priori estimates together with an application of the Aubin-Lions Lemma.


Author(s):  
Laure Fournier ◽  
Lena Costaridou ◽  
Luc Bidaut ◽  
Nicolas Michoux ◽  
Frederic E. Lecouvet ◽  
...  

Abstract Existing quantitative imaging biomarkers (QIBs) are associated with known biological tissue characteristics and follow a well-understood path of technical, biological and clinical validation before incorporation into clinical trials. In radiomics, novel data-driven processes extract numerous visually imperceptible statistical features from the imaging data with no a priori assumptions on their correlation with biological processes. The selection of relevant features (radiomic signature) and incorporation into clinical trials therefore requires additional considerations to ensure meaningful imaging endpoints. Also, the number of radiomic features tested means that power calculations would result in sample sizes impossible to achieve within clinical trials. This article examines how the process of standardising and validating data-driven imaging biomarkers differs from those based on biological associations. Radiomic signatures are best developed initially on datasets that represent diversity of acquisition protocols as well as diversity of disease and of normal findings, rather than within clinical trials with standardised and optimised protocols as this would risk the selection of radiomic features being linked to the imaging process rather than the pathology. Normalisation through discretisation and feature harmonisation are essential pre-processing steps. Biological correlation may be performed after the technical and clinical validity of a radiomic signature is established, but is not mandatory. Feature selection may be part of discovery within a radiomics-specific trial or represent exploratory endpoints within an established trial; a previously validated radiomic signature may even be used as a primary/secondary endpoint, particularly if associations are demonstrated with specific biological processes and pathways being targeted within clinical trials. Key Points • Data-driven processes like radiomics risk false discoveries due to high-dimensionality of the dataset compared to sample size, making adequate diversity of the data, cross-validation and external validation essential to mitigate the risks of spurious associations and overfitting. • Use of radiomic signatures within clinical trials requires multistep standardisation of image acquisition, image analysis and data mining processes. • Biological correlation may be established after clinical validation but is not mandatory.


2021 ◽  
Vol 183 (1) ◽  
Author(s):  
R. Alonso ◽  
V. Bagland ◽  
L. Desvillettes ◽  
B. Lods

AbstractIn this paper, we present new estimates for the entropy dissipation of the Landau–Fermi–Dirac equation (with hard or moderately soft potentials) in terms of a weighted relative Fisher information adapted to this equation. Such estimates are used for studying the large time behaviour of the equation, as well as for providing new a priori estimates (in the soft potential case). An important feature of such estimates is that they are uniform with respect to the quantum parameter. Consequently, the same estimations are recovered for the classical limit, that is the Landau equation.


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