scholarly journals Luminescence age calculation through Bayesian convolution of equivalent dose and dose-rate distributions: the D<sub>e</sub>_D<sub>r</sub> model

2021 ◽  
Author(s):  
Norbert Mercier ◽  
Jean-Michel Galharret ◽  
Chantal Tribolo ◽  
Sebastian Kreutzer ◽  
Anne Philippe

Abstract. In nature, any mineral grain (quartz or feldspar) receives a dose-rate (Dr) specific to its environment. The dose-rate distributions, therefore, reflect the micro-dosimetric context of grains of similar size. If all the grains have been well bleached at deposition, this distribution corresponds, within uncertainties, to the distribution of equivalent doses (De). Their combination (convolution of the De and Dr distributions in the De_Dr model proposed here) allows the calculation of the true depositional age. If grains whose De values are not representative of this age (hereafter called "outliers") are present in the De distribution, the model allows them to be identified before the age is calculated. As the De_Dr approach relies only on the Dr distribution, the model avoids any assumption representing the De distribution, which is usually difficult to justify. Herein, we outline the mathematical concepts of the De_Dr approach (more details are given in Galharret et al., accepted) and the exploitation of this Bayesian modelling based on an R code available in the R package 'Luminescence'. We also present a series of tests using simulated Dr and De distributions with and without outliers and show that the De_Dr approach can be an alternative to available models for interpreting De distributions.

1976 ◽  
Vol 19 (3) ◽  
pp. 404-408
Author(s):  
A. P. Yanovskii ◽  
M. F. Yudin ◽  
L. A. Popruzhko ◽  
V. V. Frolov ◽  
Yu. D. Lysak

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
Yang Cao ◽  
Wenjian Xu ◽  
Chao Niu ◽  
Xiaochen Bo ◽  
Fei Li

Large amounts of various biological networks exist for representing different types of interaction data, such as genetic, metabolic, gene regulatory, and protein-protein relationships. Recent approaches on biological network study are based on different mathematical concepts. It is necessary to construct a uniform framework to judge the functionality of biological networks. We recently introduced a knowledge-based computational framework that reliably characterized biological networks in system level. The method worked by making systematic comparisons to a set of well-studied “basic networks,” measuring both the functional and topological similarities. A biological network could be characterized as a spectrum-like vector consisting of similarities to basic networks. Here, to facilitate the application, development, and adoption of this framework, we present an R package called NFP. This package extends our previous pipeline, offering a powerful set of functions for Network Fingerprint analysis. The software shows great potential in biological network study. The open source NFP R package is freely available under the GNU General Public License v2.0 at CRAN along with the vignette.


Author(s):  
Turgay Korkut ◽  
Zeynep Itır Umaç ◽  
Bünyamin Aygün ◽  
Abdulhalik Karabulut ◽  
Sinan Yapıcı ◽  
...  

2011 ◽  
Vol 38 (4) ◽  
pp. 424-431 ◽  
Author(s):  
Alastair Cunningham ◽  
Jakob Wallinga ◽  
Philip Minderhoud

AbstractIn the OSL dating of sediment, the scatter in equivalent dose (D e) between grains is almost always larger than would be expected due to counting statistics alone. Some scatter may be caused by insufficient (partial) bleaching of some of the grains prior to deposition. In order to date partially bleached sediment, it is essential to estimate the amount of scatter caused by other processes (e.g. grain-to-grain variability in the natural dose rate). Measurements of such scatter are performed at the single-grain level; by contrast, most OSL dating is performed on multi-grain subsamples, for which grain-to-grain scatter is reduced through averaging.Here we provide a model for estimating the expected scatter (i.e. excluding that caused by partial bleaching) for multi-grain aliquots. The model requires as input the single-grain sensitivity distribution, the number of grains in the sub-samples, and the expected scatter at the single-grain level, all of which can be estimated to an adequate degree. The model compares well with measured values of scatter in D e, determined using aliquots of various sizes, and can be used to help produce a minimum-age D e from multi-grain subsamples that is consistent with single-grain data.


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