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JournalISSN: 1947-928X

International Journal of Natural Computing Research 

IGI Global
About: International Journal of Natural Computing Research is an academic journal published by IGI Global. The journal publishes majorly in the area(s): Evolutionary algorithm & Population. It has an ISSN identifier of 1947-928X. Over the lifetime, 154 publications have been published receiving 1252 citations. The journal is also known as: IJNCR.

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Journal ArticleDOI
TL;DR: It is shown that the (fuzzy) languages accepted by open evolution quantum automata obey various closure properties, and major other models of finite automata, including probabilistic, measure once quantum, measure many quantum, and Latvian quantum Automata can be simulated by the open quantum evolution automata without increasing the number of the states.
Abstract: In this paper, a model for finite automaton with an open quantum evolution is introduced, and its basic properties are studied. It is shown that the (fuzzy) languages accepted by open evolution quantum automata obey various closure properties. More importantly, it is shown that major other models of finite automata, including probabilistic, measure once quantum, measure many quantum, and Latvian quantum automata can be simulated by the open quantum evolution automata without increasing the number of the states.

87 citations

Journal ArticleDOI
TL;DR: The authors present a cognitively inspired mathematical learning framework called Neural Modeling Fields (NMF), which successfully overcomes the combinatorial complexity of associating subsets of objects with situations and demonstrates fast and reliable convergence.
Abstract: The authors present a cognitively inspired mathematical learning framework called Neural Modeling Fields (NMF). They apply it to learning and recognition of situations composed of objects. NMF successfully overcomes the combinatorial complexity of associating subsets of objects with situations and demonstrates fast and reliable convergence. The implications of the current results for building multi-layered intelligent systems are also discussed.

56 citations

Journal ArticleDOI
TL;DR: In this article, the authors analyzed the slime plasmodium's network in terms of proximity graphs and evaluated slime mould's response to contamination in urban areas with rolled oats and inoculated slime mould in Toronto area.
Abstract: Slime mould Physarum polycephalum builds up sophisticated networks to transport nutrients between distant parts of its extended body. The slime mould’s protoplasmic network is optimised for maximum coverage of nutrients yet minimum energy spent on transportation of the intra-cellular material. In laboratory experiments with P. polycephalum we represent Canadian major urban areas with rolled oats and inoculated slime mould in the Toronto area. The plasmodium spans the urban areas with its network of protoplasmic tubes. The authors uncover similarities and differences between the protoplasmic network and the Canadian national highway network, analyse the networks in terms of proximity graphs and evaluate slime mould’s network response to contamination.

41 citations

Journal ArticleDOI
TL;DR: The Metabolic P systems theory is applied for developing new physiologically based models of the glucose-insulin system, which can be applied to the Intravenous Glucose Tolerance Test.
Abstract: The Intravenous Glucose Tolerance Test is an experimental procedure used to study the glucose-insulin endocrine regulatory system. An open problem is to construct a model representing simultaneously the entire regulative mechanism. In the past three decades, several models have appeared, but they have not escaped criticisms and drawbacks. In this paper, the authors apply the Metabolic P systems theory for developing new physiologically based models of the glucose-insulin system, which can be applied to the IVGTT. Ten datasets obtained from literature were considered and an MP model was found for each, which fits the data and explains the regulations of the dynamics. Finally, each model is analysed to define a common pattern which explains, in general, the action of the glucose-insulin control system. DOI: 10.4018/jncr.2011070102 14 International Journal of Natural Computing Research, 2(3), 13-24, July-September 2011 Copyright © 2011, IGI Global. Copying or distributing in print or electronic forms without written permission of IGI Global is prohibited. results in increasing the blood glucose level by acting on liver cells and causing them to release glucose into the blood2 (Figure 1). If the plasma glucose concentration level is constantly out of the usual range, then we are in presence of blood glucose problems. In particular, when this level is constantly higher than the range upper bound (which is referred to as hyperglycemia), we are in presence of Diabetes: a dreadfully severe and pervasive illness which concerns a good number of structures in the body. Diabetes is classified into two main categories known as type I and type II, respectively. Type I, 5−10% of all categories of diabetes, results from autoimmune destruction of β-cells and the pancreas is no longer capable of making insulin. Therefore, daily insulin injections are necessary. Diabetes of type II refers to the remaining 90% and occurs when the pancreas produces insulin but cells fail to use it properly. In both the types of diabetes, the illness can lead to several complications like retinopathy, nephropathy, peripheral neuropathy and blindness. This motivates researches to study the glucose-insulin endocrine regulatory system. In particular, the glucoseinsulin system has been the object of repeated mathematical modelling attempts. The majority of the proposed models were devoted to the study of the glucose-insulin dynamics by considering experimental data obtained by the intravenous glucose tolerance test, shortly IVGTT, and the oral glucose tolerance test, shortly OGTT. In these models, the insulinglucose system is assumed to be composed of two linked subsystems modelling the insulin action and the glucose kinetics, respectively. Since the action of insulin is delayed with respect to plasma glucose, the subsystems of insulin action typically includes a delay. The intravenous glucose tolerance test focuses on the metabolism of glucose in a period of 3 hours starting from the infusion of a bolus of glucose at time t = 0. It is based on the assumption that, in a healthy person, the glucose concentration decreases exponentially with time following the loading dose (Figure 2). It has been recommended as a method to assess the use of insulin in order to identify subjects which may be diabetics (National Diabetes Data Group, 1979). However, considering the limits of the existing mathematical models, a need exists to have reliable mathematical models representing the glucose-insulin system. The mere fact that several models have been proposed (Boutayeb & Chetouani, 2006; Makroglou, Li, & Kuang, 2006; Mari, 2002) shows that mathematical and physiological considerations have to be carefully integrated when attempting to represent the glucose-insulin regulatory mechanism. In particular, in order to model the IVGTT, a reasonably simple model is required. It has to have a few parameters to be estimated and has to have dynamics consistent with physiology and experimental data. Further, the model formulation, while applicable to model the IVGTT, should be Figure 1. The glucose homeostasis International Journal of Natural Computing Research, 2(3), 13-24, July-September 2011 15 Copyright © 2011, IGI Global. Copying or distributing in print or electronic forms without written permission of IGI Global is prohibited. logically and easily extensible to model other envisaged experimental procedures. 2. MATHEMATICAL MODELS OF THE INTRAVENOUS GLUCOSE TOLERANCE TEST A variety of mathematical models, statistical methods and algorithms have been proposed to understand different aspects of diabetes. In this section we briefly review the two mathematical models which had the most important impact in diabetology for modelling the intravenous glucose tolerance test. They have been useful to assess physiological parameters and to study the glucose-insulin interactions. However, they have not escaped from criticism and drawbacks. Although several other models have been proposed (Bergman, Finegood, & Ader, 1985), the real start of modelling glucose-insulin dynamics is due to the minimal model developed in Bergman, Ider, Bowden, and Cobelli (1979) and Toffolo, Bergman, Finegood, Bowden, and Cobelli (1980). It has been characterized as the simplest model which is able to describe the glucose metabolism reasonably well by using the smallest set of identifiable and meaningful parameters (Bergman et al., 1979; Pacini & Bergman, 1986). Several versions based on the minimal model have been proposed, and the reader can find further information on them in Bergman et al. (1985) and Cobelli and Mari (1983). The minimal model has been formulated by using the following system of differential equations:

35 citations

Journal ArticleDOI
TL;DR: The emphasis of this paper will be on the formalization and critical analysis of the set of contributions produced along almost one decade of research in this specific theme, together with the provision of insights for further extensions.
Abstract: In this paper, a review of the conceptual and practical aspects of the aiNet (Artificial Immune Network) family of algorithms will be provided. This family of algorithms started with the aiNet algorithm, proposed in 2002 for data clustering and, since then, several variations have been developed for data clustering, biclustering and optimization in general. Although the algorithms will be positioned with respect to other pertinent approaches from the literature, the emphasis of this paper will be on the formalization and critical analysis of the set of contributions produced along almost one decade of research in this specific theme, together with the provision of insights for further extensions.

33 citations

Performance
Metrics
No. of papers from the Journal in previous years
YearPapers
20231
20221
20217
202017
201916
201816