Hyperspectral Unmixing Overview: Geometrical, Statistical, and Sparse Regression-Based Approaches

Imaging spectrometers measure electromagnetic energy scattered in their instantaneous field view in hundreds or thousands of spectral channels with higher spectral resolution than multispectral cameras. Imaging spectrometers are therefore often referred to as hyperspectral cameras (HSCs). Higher spectral resolution enables material identification via spectroscopic analysis, which facilitates countless applications that require identifying materials in scenarios unsuitable for classical spectroscopic analysis. Due to low spatial resolution of HSCs, microscopic material mixing, and multiple scattering, spectra measured by HSCs are mixtures of spectra of materials in a scene. Thus, accurate estimation requires unmixing. Pixels are assumed to be mixtures of a few materials, called endmembers. Unmixing involves estimating all or some of: the number of endmembers, their spectral signatures, and their abundances at each pixel. Unmixing is a challenging, ill-posed inverse problem because of model inaccuracies, observation noise, environmental conditions, endmember variability, and data set size. Researchers have devised and investigated many models searching for robust, stable, tractable, and accurate unmixing algorithms. This paper presents an overview of unmixing methods from the time of Keshava and Mustard's unmixing tutorial [1] to the present. Mixing models are first discussed. Signal-subspace, geometrical, statistical, sparsity-based, and spatial-contextual unmixing algorithms are described. Mathematical problems and potential solutions are described. Algorithm characteristics are illustrated experimentally.Comment: This work has been accepted for publication in IEEE Journal of Selected Topics in Applied Earth Observations and Remote Sensin

Nonlinear unmixing of hyperspectral images: Models and algorithms

When considering the problem of unmixing hyperspectral images, most of the literature in the geoscience and image processing areas relies on the widely used linear mixing model (LMM). However, the LMM may be not valid, and other nonlinear models need to be considered, for instance, when there are multiscattering effects or intimate interactions. Consequently, over the last few years, several significant contributions have been proposed to overcome the limitations inherent in the LMM. In this article, we present an overview of recent advances in nonlinear unmixing modeling

Novel characterization method of impedance cardiography signals using time-frequency distributions

The purpose of this document is to describe a methodology to select the most adequate time-frequency distribution (TFD) kernel for the characterization of impedance cardiography signals (ICG). The predominant ICG beat was extracted from a patient and was synthetized using time-frequency variant Fourier approximations. These synthetized signals were used to optimize several TFD kernels according to a performance maximization. The optimized kernels were tested for noise resistance on a clinical database. The resulting optimized TFD kernels are presented with their performance calculated using newly proposed methods. The procedure explained in this work showcases a new method to select an appropriate kernel for ICG signals and compares the performance of different time-frequency kernels found in the literature for the case of ICG signals. We conclude that, for ICG signals, the performance (P) of the spectrogram with either Hanning or Hamming windows (P¿=¿0.780) and the extended modified beta distribution (P¿=¿0.765) provided similar results, higher than the rest of analyzed kernels.Peer ReviewedPostprint (published version

Source Separation in Chemical Analysis : Recent Achievements and Perspectives

International audienceSource separation is one of the most relevant estimation problems found in chemistry. Indeed, dealing with mixtures is paramount in different kinds of chemical analysis. For instance, there are some cases where the analyte is a chemical mixture of different components, e.g., in the analysis of rocks and heterogeneous materials through spectroscopy. Moreover, a mixing process can also take place even when the components are not chemically mixed. For instance, in ionic analysis of liquid samples, the ions are not chemically connected, but, due to the lack of selectivity of the chemical sensors, the acquired responses may be influenced by ions that are not the desired ones. Finally, there are some situations where the pure components cannot be isolated chemically since they appear only in the presence of other components. In this case, BSS may provide these components that cannot be retrieved otherwise. In this paper, our aim is to shed some light on the use of BSS in chemical analysis. In this context, we firstly provide a brief overview on source separation (Section II), with particular attention to the classes of linear and nonlinear mixing models (Sections III and IV, respectively). Then, (in Section V), we will give some conclusions and focus on challenging aspects that are found in chemical analysis. Although dealing with a relatively new field of applications, this article is not an exhaustive survey of source separation methods and algorithms, since there are solutions originated in closely related domains (e.g. remote sensing and hyperspectral imaging) that suit well several problems found in chemical analysis. Moreover, we do not discuss the supervised source separation methods, which are basically multivariate regression techniques, that one can find in chemometrics