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  • 1
    Keywords: Atom ; Fulleren ; Fullerene ; Nanocar ; Nanomaterial ; Nanotube ; Transport ; carbon nanotubes ; electricity
    Description / Table of Contents: The 2007 ARW “Using Carbon Nanomaterials in Clean-Energy Hydrogen Systems” (UCNCEHS’2007) was held in September 22–28, 2007 in the remarkable town Sudak (Crimea, Ukraine) known for its heroic and unusual fate. In the tradition of the earlier conferences, UCNCEHS’2007 meeting served as an multidisciplinary forum for the presentation and discussion of the most recent research on transition to hydrogen-based energy systems, technologies for hydrogen production, storage, utilization, carbon nanomaterials processing and chemical behavior, energy and environmental problems. The aim of UCNCEHS’2007 was to provide the wide overview of the latest scientific results on basic research and technological applications of hydrogen interactions with carbon materials. The active representatives from research/academic organizations and governmental agencies could meet, discuss and present the most recent advances in hydrogen concepts, processes and systems, to evaluate current progress and to exchange academic information, to identify research needs and future development in this important area. This ARW should help further the progress of hydrogen-based science and promote the role of hydrogen and carbon nanomaterials in the energy field.
    ISBN: 9781402088988
    Language: English
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  • 2
    Keywords: Assessment ; Malaria ; Public Health ; Scale ; Weather ; climate change ; public health policy ; temperature
    Description / Table of Contents: Awareness that many key aspects of public health are strongly influenced by climate is growing dramatically, driven by new research and experience and fears of climate change and the research needed to underpin policy developments in area is growing rapidly . This awareness has yet to translate into a practical use of climate knowledge by health policy-makers. Evidence based policy and practice is the mantra of the health sector. If climate scientists are to contribute effectively to health policy at local and global scales then careful empirical studies must be undertaken – focused on the needs of the public health policy and decision-makers. Results presented at the Wengen conference make clear that the science and art of integrating climate knowledge into the control of climate sensitive diseases on a year to year time frame as well as careful assessments of the potential impacts of climate change on health outcomes over longer time frames is advancing rapidly on many fronts. This includes advances in the empirical understanding of mechanisms, methodologies for modeling future impacts, new partnership developments between the health and climate community along with access to relevant data resources, and education and training. In a rapidly evolving field this book provides a snapshot of these emerging themes.
    Pages: Online-Ressource (X, 232 pages)
    ISBN: 9781402068775
    Language: English
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  • 3
    Keywords: Air ; Chlor ; GSM-Postponed Project ; Manual ; Oxide ; Water ; bacteria ; microorganism ; pollution ; production ; soil ; toxicity
    Description / Table of Contents: Environmental Chemistry: Fundamentals, by Jorge Ibanez et al., is an exceptionally useful and well organized book. After reviewing basic chemical concepts, Environmental Chemistry: Fundamentals quickly progresses to more advanced and contemporary applications including ozone depletion, physiochemical and biological treatment of pollutants, and green chemistry. The chemistry of processes of the atmosphere, lithosphere and hydrosphere are covered in detail and the effects of pollutants on each of these chemical processes are extensively considered, as are their effects on the biosphere. The book also has an experimental companion, Environmental Chemistry: Microscale Laboratory Experiments, which includes an array of environmental chemistry experiments that can be readily performed at the microscale level. Ideas for additional open-ended projects are provided for all experiments, and they impart a thorough introduction to environmental experimentation. I strongly recommend Environmental Chemistry: Fundamentals and its experimental accompaniment, Environmental Chemistry: Microscale Laboratory Experiments. Dr. Zvi Szafran Vice President for Academic Affairs and Professor of Chemistry Southern Polytechnic State University Our Earth is a remarkable reaction vessel. It is of paramount importance that students grow in their understanding and awareness of the astounding effects that chemistry and biochemistry have on our environment…and why they are so significant to our present and future hopes as a civilization. Environmental Chemistry: Microscale Laboratory Experiments, intended to complement lessons in the companion textbook Environmental Chemistry: Fundamentals, covers the chemical and biochemical processes that take place in air, water, soil, and living systems. The corresponding experiments range from the characterization of aqueous media to pollutant-treatment schemes. For increased safety, as well as for reduced costs, wastes, and environmental damage, the experiments are presented at the microscale level. Pre- and post-laboratory exercises and open-ended projects accompany each experiment, to develop problem-solving skills and initiative among students.
    Pages: Online-Ressource (XII, 238 pages)
    ISBN: 9780387494937
    Language: English
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  • 4
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    Bulletin of mathematical biology 15 (1953), S. 311-338 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract The partial differential equation of the random walk problem with persistence of direction and external bias is derived. By persistence of direction or internal bias we mean that the probability a particle will travel in a given direction need not be the same for all directions, but depends solely upon the particle's previous direction of motion. The external bias arises from an anisotropy of the medium or an external force on the particle. The problem is treated by considering that the net displacement of a particle arises from two factors, namely, that neither the probability of the particle traveling in any direction after turning nor the distance the particle travels in a given direction need be the same for all directions. A modified Fokker-Planck equation is first obtained using the assumptions that the particles have a distribution of travel times and speeds and that the average time of travel between turns need not be zero. The fional equation incopporating the assumption of a persistence of direction and an external bias is then derived. Applications to the study of diffusion and to long-chain polymers are then made.
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  • 5
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    Bulletin of mathematical biology 15 (1953), S. 383-383 
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  • 6
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    Bulletin of mathematical biology 15 (1953), S. 385-385 
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    Bulletin of mathematical biology 15 (1953), S. 367-381 
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    Notes: Abstract The transmission of some information or behavior pattern is treated as a flow of “particles” which execute random motions over a population of individuals and which may multiply or disappear. Equations are derived for the number density of these “particles” and from this is calculated the number of individuals through which the “particles” have passed. The results are applied to a number of situations such as 1) uniform spatial distribution with multiplication factor decreasing with time because of loss of interest or confusion of the information, 2) multiplication factor constant but the rate of spreal decreasing with multiple hearings, 3) one-dimensional region with a small starting region with or without an absorbing barrier 4) two-dimensional region with absorbing barrier, 5) continous sources of information within a small region in one dimension, 6) uniform spatial distribution in which individuals do not respond to more than one hearing.
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  • 8
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    Bulletin of mathematical biology 15 (1953), S. 387-394 
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    Notes: Abstract A situation is considered in which a fluid containing a substance flows through a vessel at a constant rate, the substance being permeable to the vessel wall. In the region outside the vessel there is supposed to be rapid mixing in the direction perpendicular to the axis of the vessel but no mixing longitudinally. The solution for the spatial distribution at any time is given for the case of an arbitrary initial distribution along the vessel length in the absence of an input. The solution is also given for the case of a single impulsive input, the concentration being initially zero everywhere.
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  • 9
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    Bulletin of mathematical biology 15 (1953), S. 431-476 
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    Notes: Abstract Organisms orient themselves to a stimulus by two general methods. One method is by directed orientation (taxis); the other is by undirected locomotory reaction (kinesis). An equation, and the methods for finding the necessary parameters of this equation, is derived for the distribution of organisms within a container, with the following limitations: (1) the organisms have no accommodation, (2) they are always active, and (3) the stimulus changes slowly with position. Necessary modifications of the equation are then derived, so that the last two limitations may be eliminated. The equation cannot be solved excatly because of its complexity; hence an approximation method must be used. This method is discussed, an approximate solution is found, and a time constant for equilibrium to be established is derived. Applications tovarious experiments in the literature are then made with fairly satisfactory results. A new interpretation of the theory of klino-kinesis with accommodation is found upon application of the equations developed to experimental work. Further limitations and uses of these equations are then discussed.
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    Bulletin of mathematical biology 15 (1953), S. 501-507 
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    Notes: Abstract Certain parameters are defined which roughly characterize the internal structure of networks. A given network structure uniquely determines the values of the parameters, but the reverse is not true. The parameters therefore define certain classes of networks. One of the parameters, thedispersion D(S) gives an indication of the “compactness” of the internal structure. Addition theorems and inequalities are derived relating the dispersions of sub-systems to the dispersion of the complete structure.
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    Bulletin of mathematical biology 15 (1953), S. 489-500 
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    Notes: Abstract A mathematical theory is developed which permits the determination of certain parameters of an inhomogenous tissue, such as a nerve trunk without its epineurium. The parameters are the permeability coefficients for entrance into an exit of a substance from the nerve fibers, and the diffusion coefficient of the interstitial material. The experimental data required are the dimensions of the cross-section, the average diameter of the fibers, and the ratio of the cross-sectional are of the fibers to the total cross-section, as well as the time course of the decrease of the fraction of the substance left in the nerve trunk, when the trunk is immersed in a bathing solution containing none of it.
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  • 12
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    Bulletin of mathematical biology 15 (1953), S. 509-522 
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    Notes: Abstract A model based on enzyme localization is developed which gives rise to an apparent active transport of a metabolite into or out of cells. The model is applied to three simple situations, using Fick's equation and the Rashevsky approximation. It is shown that the apparent efficiency can be made as large as desired if, for constant reaction, the outer cell region is made sufficiently small, or, for autocatalytic reaction, if the metabolite concentration in the outer region is sufficiently small. The physical limitations imposed by this mechanism are developed for all three situations.
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  • 13
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    Bulletin of mathematical biology 15 (1953), S. 523-533 
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    Notes: Abstract A previously derived iteration formula for a random net was applied to some data on the spread of information through a population. It was found that if the axon density (the only free parameter in the formula) is determined by the first pair of experimental values, the predicted spread is much more rapid than the observed one. If the successive values of the “apparent axon density” are calculated from the successive experimental values, it is noticed that this quantity at first suffers a sharp drop from an initial high value to its lowest value and then gradually “recovers”. An attempt is made to account for this behavior of the apparent axon density in terms of the “assumption of transitivity”, based on a certain socio-structural bias, namely, that the likely contacts of two individuals who themselves have been in contact are expected to be strongly overlapping. The assumption of transitivity leads to a drop in the apparent axon density from an arbitrary initial value to the vicinity of unity (if the actual axon density is not too small). However, the “recovery” is not accounted for, and thus the predicted spread turns out to beslower than the observed.
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    Bulletin of mathematical biology 15 (1953), S. 535-546 
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    Notes: Abstract The assumption of transitivity treated in part I is modified in various ways to describe an information-diffusion process, in which a certain amount of randomness of contact does occur. In one model a parameter is introduced which is indicative of a tendency to go beyond one's immediate vicinity to spread the information as the vicinity becomes saturated with knowers. In another model the randomness appears in the assumption that new knowers are uniformly distributed among the knowers. Two of the equations thus derived, each with two free parameters are in good agreement with experimental results.
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  • 15
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    Bulletin of mathematical biology 52 (1990), S. 153-197 
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    Notes: Abstract It is suggested that a system of chemical substances, called morphogens, reacting together and diffusing through a tissue, is adequate to account for the main phenomena of morphogenesis. Such a system, although it may originally be quite homogeneous, may later develop a pattern or structure due to an instability of the homogeneous equilibrium, which is triggered off by random disturbances. Such reaction-diffusion systems are considered in some detail in the case of an isolated ring of cells, a mathematically convenient, though biologically unusual system. The investigation is chiefly concerned with the onset of instability. It is found that there are six essentially different forms which this may take. In the most interesting form stationary waves appear on the ring. It is suggested that this might account, for instance, for the tentacle patterns onHydra and for whorled leaves. A system of reactions and diffusion on a sphere is also considered. Such a system appears to account for gastrulation. Another reaction system in two dimensions gives rise to patterns reminiscent of dappling. It is also suggested that stationary waves in two dimensions could account for the phenomena of phyllotaxis. The purpose of this paper is to discuss a possible mechanism by which the genes of a zygote may determine the anatomical structure of the resulting organism. The theory does not make any new hypotheses; it merely suggests that certain well-known physical laws are sufficient to account for many of the facts. The full understanding of the paper requires a good knowledge of mathematics, some biology, and some elementary chemistry. Since readers cannot be expected to be experts in all of these subjects, a number of elementary facts are explained, which can be found in text-books, but whose omission would make the paper difficult reading.
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    Bulletin of mathematical biology 52 (1990), S. 319-334 
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  • 17
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    Bulletin of mathematical biology 52 (1990), S. 335-337 
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    Bulletin of mathematical biology 52 (1990), S. I 
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    Bulletin of mathematical biology 52 (1990), S. 335-348 
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    Notes: Abstract The classical metaphor of the genetic program written in the DNA nucleotidic sequences is reconsidered. Recent works on algorithmic complexity and logical properties of computer programs and data are used to question the explanatory value of that metaphor. Structural properties of strings are looked for which would be necessary to apply to DNA sequences if the metaphor is to be taken literally. The notion of sophistication is used to quantify meaningful complexity and to distinguish it from classical computational complexity. In this context, the distinction between program and data becomes relevant and an alternative metaphor of DNA as data to a parallel computing network embedded in the global geometrical and biochemical structure of the cell is discussed. An intermediate picture of an evolving network emerges as the most likely where the output of the cellular computing network can produce, at a different time scale, changes in the structure of the network itself by means of changes in the DNA activity patterns.
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    Bulletin of mathematical biology 52 (1990), S. 349-358 
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    Notes: Abstract When two strings of symbols are aligned it is important to know whether the observed number of matches is better than that expected between two independent sequences with the same frequency of symbols. When strings are of different lengths, nulls need to be inserted in order to align the sequences. One approach is to use simple approximations of sampling for replacement. We describe an algorithm for exactly determining the frequencies of given numbers of matches, sampling without replacement. This does not lead to a simple closed form expression. However we show examples where sampling with, or without, replacement give very similar results and the simple approach may be adequate for all but the smallest cases.
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    Bulletin of mathematical biology 52 (1990), S. 509-525 
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    Notes: Abstract Pairwise optimal alignments between three or more sequences are not necessarily consistent as a whole, but consistent and inconsistent residues are usually distributed in clusters. An efficient method has been developed for locating consistent regions when each pairwise alignment is given in the form of a “skeletal representation” (Bull. math. Biol. 52, 359–373). This method is further extended so that the combination of pairwise alignments that gives the greatest consistency is found when possibly many alignments are equally optimal for each pairwise comparison. A method for acceleration of simultaneous multiple sequence alignment is proposed in which consistent regions serve as “anchor points” limiting application of direct multi-way alignment to the rest of “inconsistent” regions.
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    Bulletin of mathematical biology 52 (1990), S. 527-534 
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    Notes: Abstract Sufficient conditions are given for the unlimited growth or otherwise in multitype population size dependent Galton-Watson processes. These conditions are given in terms of moments of offspring distributions and extend known conditions for processes with one type.
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    Bulletin of mathematical biology 52 (1990), S. 535-547 
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    Notes: Abstract The variability of the duration of the cell cycle is explained by the phenomenon of sensitive dependence upon initial conditions; as may occur in deterministic non-linear systems. Chaotic dynamics of a system is the result of this sensitive dependence. First a deterministic system is formulated that is equivalent to the Smith-Martin transition probability model of the cell cycle. Next the model is extended to a dynamic process that ranges over the cell generations. A deterministic non-linear relationship between the cycle time of the mother and daughter cell is established. It clarifies the variability of mother-daughter correlation for the different cell types. The model is fitted to two different cell cultures; it shows that the graph of the non-linear relation has the same shape for different cell types.
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    Bulletin of mathematical biology 52 (1990), S. 583-596 
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    Bulletin of mathematical biology 52 (1990), S. I 
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    Bulletin of mathematical biology 52 (1990), S. 549-582 
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    Notes: Abstract Recently a mathematical model of the prevascular phases of tumor growth by diffusion has been investigated (S. A. Maggelakis and J. A. Adam,Math. Comput. Modeling, in press). In this paper we examine in detail the results and implications of that mathematical model, particularly in the light of recent experimental work carried out on multicellular spheroids. The overall growth characteristics are determined in the present model by four parameters:Q, γ, b, andδ, which depend on information about inhibitor production rates, oxygen consumption rates, volume loss and cell proliferation rates, and measures of the degree of non-uniformity of the various diffusion processes that take place. The integro-differential growth equation is solved for the outer spheroid radiusR 0(t) and three related inner radii subject to the solution of the governing time-independent diffusion equations (under conditions of diffusive equilibrium) and the appropriate boundary conditions. Hopefully, future experimental work will enable reasonable bounds to be placed on parameter values referred to in this model: meanwhile, specific experimentally-provided initial data can be used to predict subsequent growth characteristics ofin vitro multicellular spheroids. This will be one objective of future studies.
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    Notes: Abstract Workers of the speciesLeptothorax acervorum show age-polyethism, they start their life as broodworkers and later on they become nestworkers and foragers. Nestworkers and foragers of this ant species are inactive for 72% and 15% of the total time respectively. The short bursts of activity within the nest do not occur randomly but are synchronized so that the whole nest population exhibits nonperiodic pulses of activity: the ants were seen to wake each other actively. In addition starvation experiments were done to assess whether ants react upon food availability. In appeared that during a longlasting period of starvation the proportion of active ants in the nest is at a higher approximately constant level.
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    Circuits, systems and signal processing 9 (1990), S. 501-502 
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    Circuits, systems and signal processing 9 (1990), S. 503-503 
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    Circuits, systems and signal processing 9 (1990), S. 505-505 
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    Circuits, systems and signal processing 9 (1990), S. 171-180 
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    Notes: Abstract For ann-by-n nonnegative matrixP, we consider the entrywise harmonic meanH, geometric meanG, and arithmetic meanA, ofP and PT. Simple proofs are given for the inequalities ρ(H)≤ρ(G)≤ p(P)≤ ρ(A), and attention is focused upon characterization of the case of equality in each of these six inequalities. In caseP is irreducible, ρ(G)=p(P) exactly whenP is diagonally similar to a symmetric matrix, and several other equivalent conditions for diagonal symmetrizability ofP are collected together here. Other conditions which arise involve further variations upon symmetry, and may be viewed as algebraic descriptions of various features of symmetry. A tool of interest is a slight variation upon a recent characterization of the Perron root.
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    Circuits, systems and signal processing 9 (1990), S. 197-212 
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    Notes: Abstract A new class of shorted operators is considered. The shorted operator has an intimate relationship with electrical networks and has been extensively studied. In this work we consider the class of matrices with row and column spans in specified linear subspaces and dominated in a given partial order by a matrixA. If this class of matrices has an unique maximal element under the partial order, then this maximal element is called the shorted matrix ofA relative to the given linear subspaces and the relevant partial order. We study the shorted matrix under the star order of Drazin, the minus order, and also under partial orders induced by the minimum norm and least squares g-inverses. The parallel sum of matrices is intimately related to the shorted matrix and results are given for parallel addition.
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    Circuits, systems and signal processing 9 (1990), S. 223-228 
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    Notes: Abstract A new variational characterization of the solution of a matrix Riccati equation is presented. The characterization is given as the maximum Hermitian matrix that makes a certain compound matrix Hermitian positive semidefinite. The shorted operator (Schur complement) applied to the compound matrix produces the Riccati equation.
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    Circuits, systems and signal processing 9 (1990), S. 271-300 
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    Notes: Abstract An eigenstructure-based method for direction finding in the presence of sensor gain and phase uncertainties is presented. The method provides estimates of the Directions of Arrival (DOA) of all the radiating sources as well as calibration of the gain and phase of each sensor in the observing array. The technique is not limited to a specific array configuration and can be implemented in a'ny eigenstructure-based DOA system to improve its performance.
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    Circuits, systems and signal processing 9 (1990), S. 319-341 
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    Notes: Abstract The effects of system parameter uncertainties on system performance are always of great concern to the system designer. It is desirable to knowa priori estimates of the system response, subject to parameter uncertainties. In the following we propose using interval analysis techniques to establish estimates of system performance (e.g., envelopes of time response and frequency response). The results which we obtain constitute generalizations of existing work. Specifically, existing results address systems which are described by linear ordinary differential equations which are endowed with a single parameter belonging to an interval. In the present results we address systems described by linear or nonlinear ordinary difference equations endowed with more than one parameter belonging to intervals.
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    Circuits, systems and signal processing 9 (1990), S. 343-364 
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    Notes: Abstract We consider general input-output systems governed by nonlinear operator equations that relate the system's input, state, and output. The systems under consideration need not be of a feedback type. Assuming that the governing equations depend on a parameterA in a linear space that is allowed to vary in a vicinity Nr(A0) of a “nominal” valueA 0, we study conditions under which the system is stable for each A∈Nr (A0), i.e., when the system is robust. By stability we essentially mean that the input-output map is continuous. Depending on the type of continuity used, two concepts of robustness are introduced. The main theorem shows that a certain generalized monotonicity condition imposed on the nominal system combined with a Lipschitz-like condition imposed on the perturbed system guarantees robustness. Moreover, several particular cases of the governing equations are investigated. As examples, we consider (1) a singular system of nonlinear ordinary differential equations (a semistate equation), (2) a feedback system, and (3) a feedback, feedforward system. At the end of this paper some extensions and modifications of the presented theory are discussed.
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    Circuits, systems and signal processing 9 (1990), S. 367-382 
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    Notes: Abstract The subject of this paper is the relation of differential-algebraic equations (DAEs) to vector fields on manifolds. For that reason, we introduce the notion of a regular DAE as a DAE to which a vector field uniquely corresponds. Furthermore, a technique is described which yields a family of manifolds for a given DAE. This socalled family of constraint manifolds allows in turn the formulation of sufficient conditions for the regularity of a DAE, and the definition of the index of a regular DAE. We also state a method for the reduction of higher-index DAEs to lower-index ones that can be solved without introducing additional constants of integration. Finally, the notion of realizability of a given vector field by a regular DAE is introduced, and it is shown that any vector field can be realized by a regular DAE. Throughout this paper the problem of path-tracing is discussed as an illustration of the mathematical phenomena.
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    Circuits, systems and signal processing 9 (1990), S. 409-420 
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    Notes: Abstract The influence of the asymmetry parameterk on the extent and form of the stability region for second-order fixed-point coupled-form digital filters is analyzed. In particular, by extending the results of a previous paper by the same authors, the stability regions for filters with roundoff quantizers are first shown. Then, the corresponding results for filters with either two or four value-truncation quantizers are derived. It turns out that the shape of the stability areas is rather odd because of the asymmetry of the quantization characteristic.
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    Circuits, systems and signal processing 9 (1990), S. 435-448 
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    Notes: Abstract Iterated-integral operators calledp-powers arise in the theory of representations of nonlinear systems. In a recent paper, necessary and sufficient conditions are given for such operators to be stable in a standard sense, and it is shown that a well-known sufficient condition is not necessary for allp ≥ 2. Here corresponding results are given for discrete-time cases.
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    Circuits, systems and signal processing 9 (1990), S. 421-433 
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    Notes: Abstract The paper first briefly reviews some subspace techniques for high-resolution array processing. It is shown that existing high-resolution techniques like the MUSIC algorithm are based on visual inspection of the spatial spectrum. It is not a scientifically valid means of assessing resolution of a spectrum estimator. The paper then proposes a technique based on a combination of optimal processing and signal subspace extraction for high-resolution array processing. Numerical results show that the proposed technique not only achieves superresolution of the spectrum, but also provides power estimates of the arrivals.
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    Circuits, systems and signal processing 9 (1990), S. 449-500 
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    Notes: Abstract Fourier transform algorithms are described using tensor (Kronecker) products and an associated class of permutations. Algebraic properties of tensor products and the related permutations are used to derive variants of the Cooley-Tukey fast Fourier transform algorithm. These algorithms can be implemented by translating tensor products and permutations to programming constructs. An implementation can be matched to a specific computer architecture by selecting the appropriate variant. This methodology is carried out for the Cray X-MP and the AT&T DSP32.
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    Bulletin of mathematical biology 15 (1953), S. 1-13 
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    Notes: Abstract The impressed field, “Window Field” (WF), due to a half-wave action potential on a muscle fiber, has been calculated on the basis of potential theory. It has been shown that in spite of the small intensity of the field, its integrated action can transfer the energy needed to induce, contraction from the membrane to the interior of the fiber. The energy of polarization has been found to be sufficient to exceed the energy of, thermal agitation on that length of fiber, which can be identified as the length of a sarcomere. The changes of ion concentration, caused by the WF, if calculated on the assumption of the semipermeability of theZ membranes, was found to be equal to the changes necessary to induce contraction of actomyosinin vitro.
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    Bulletin of mathematical biology 15 (1953), S. 15-21 
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    Notes: Abstract Some general properties of the solution of the diffusion equation are deduced for the steady-state, spherically symmetric system. On the basis of these developments some results of N. Rashevsky (Bull. Math. Biophysics,11, 15, 1949) are discussed and the results of a previous investigation (Hearon,Bull. Math. Biophysics,12, 135, 1950b) are extended to more general conditions. In particular these extensions apply to the flow of a soluteagainst its concentration gradient, the nonzero gradient of an inert metabolite, and theaccumulation or exclusion of an inert metabolite in a metabolic system.
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    Bulletin of mathematical biology 15 (1953), S. 23-31 
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    Notes: Abstract The approximation method of N. Rashevsky is discussed and reviewed. It is shown that in addition to theexplicit assumptions and approximations there is involved the assumption that the rate of metabolism is the same at every point in the cell and that theaverage rate of metabolism is different from zero. An expression is given for the error in the approximate method when the rate of metabolism is any function of the concentration. It is also shown that a solution in theform of that obtained by the approximate method is not possible if the generalized laws of diffusion are assumed to apply.
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    Bulletin of mathematical biology 15 (1953), S. 33-42 
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    Notes: Abstract Rate equations for the enzymatic oxidation of succinic acid are derived on the assumption that when a single molecule of substrate combines with an enzyme molecule, it can do so with either one or two sites on the enzyme, and that oxidation occurs only in the second case. In addition it is assumed that the product of the reaction, fumaric acid, combines reversibly with the enzyme. With certain enzyme preparations the data fitted such an equation satisfactorily. In others the rate was that of a first-order reaction, but addition of cytochrome changed it to the former type. It was concluded that the transfer of hydrogen to oxygen was a first-order reaction and dominated the whole rate when enzyme preparations were used which had been washed relatively free of cytochrome. When the limiting factor was succino-dehydrogenase the rates followed the new equation. Criteria for recognizing noncompetitive inhibition are given, and inhibition by di-tertiary butyl peroxide was shown to be of this type.
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    Bulletin of mathematical biology 15 (1953), S. 43-47 
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    Notes: Abstract This paper deals with the following question: Which distributions of radiosensitivity in a population can lead to an exponential survival curve? The problem is solved exactly, with statistical fluctuations in dose fully accounted for. It is shown that only an exponential distribution of sensitivities can give rise to an exponential survival curve.
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    Bulletin of mathematical biology 15 (1953), S. 49-61 
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    Notes: Abstract An approximation method is introduced which enables a number of diffusion-type problems to be solved in an approximate but simple manner. Many cases require only the solution of a simple first-order differential equation. The method is applied to a number of cases in which the exact solutions are available. A comparison shows that the method is quite satisfactory in these cases. The method is applied to diffusion problems with rate of consumption proportional to concentration or to the square of the concentration. In the latter case, the result obtained is essentially the same as that found by H. G. Landau (1950) after elaborate calculations.
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    Bulletin of mathematical biology 15 (1953), S. 83-91 
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    Notes: Abstract It is shown that a slight modification of a model of excitatory phenomena in irritable tissues, which has been treated before, exhibits spontaneous oscillations. The frequency of these oscillations and the time-course of the potential across the model membrane have been determined, together with the dependence of some of their characteristics on some important parameters, particularly (Ca++).
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    Bulletin of mathematical biology 15 (1953), S. 73-81 
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    Notes: Abstract It is demonstrated that, if the variations of viscosity throughout a cell are considered, swelling stresses may produce elongation and division. To do this it is necessary to generalize Betti's theorem to cover systems containing viscosity gradients and such a generalization is presented. On the basis of two special assumptions it is shown that most of the results of the diffusion drag theory of cell division may be duplicated by the present theory.
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    Bulletin of mathematical biology 15 (1953), S. 63-71 
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    Notes: Abstract The theory of imitative behavior, developed previously, is applied to the case of two social groups which are separated spatially. If the information of each group as to the behavior of the other is complete, the case reduces to that of a single group. When any information is lacking at all, the two groups are independent. If we have two mutually exclusive behaviorsA andB, all four combinationsAA, AB, BA, andBB are possible. If the mutual information gradually increases from zero, then for a certain value of it, the group which is more informed about the behavior of the other will change to that behavior if it did not already exhibit it. If for constant information the size of the group increases, then above a certain threshold value, the larger group imposes its behavior on the smaller.
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    Bulletin of mathematical biology 15 (1953), S. 103-104 
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    Bulletin of mathematical biology 15 (1953), S. 107-107 
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    Bulletin of mathematical biology 15 (1953), S. 105-106 
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    Bulletin of mathematical biology 15 (1953), S. 93-101 
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    Notes: Abstract Local regulation of blood flow as determined by capillary diameter and the number of open capillaries in a region is considered. The local changes in capillary diameter and in the number of open capillaries are assumed to be due to concentration changes of a diffusible, nonspecified metabolite. This metabolite is produced in the tissue and carried away by the blood stream. Using these assumptions and applying pertinent data on capillaries, deductions are made concerning: (a) the law of blood flow as a function of temperature and capillary radius for the hyperemia of high temperature, (b) high flow as it depends on metabolism during strenuous exercise of muscle, and (c) a first approximation to the time duration of occlusion hyperemia.
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    Bulletin of mathematical biology 15 (1953), S. 109-109 
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    Bulletin of mathematical biology 15 (1953), S. 143-148 
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    Notes: Abstract The necessary and sufficient condition is given forn integers to be the score structure of a society with a dominance relation. A proof is also given for a theorem showing that there are members who dominate every other member either directly or indirectly through a single intermediate member.
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    Bulletin of mathematical biology 15 (1953), S. 111-119 
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    Notes: Abstract On the basis of a previous general formulation (Bull. Math. Biophysics,15, 21–29, 1953a) a discussion is given of the error in the approximation method of N. Rashevsky. This error, inherent in the method when the metabolic rate is different at each point in the cell, is discussed in detail and numerical values are presented for two particular cases: the rate proportional to the concentration and the rate a prescribed function of the spatial coordinates. It is shown that the formulation for the first case also applies to several other cases, that the error is negligible provided the rate is sufficiently small, and that the error is fairly sensitive to the cell size. If the rate depends upon the coordinatesalone a small rate is not sufficient to insure a negligible error. The relations between the exact method, the standard approximate method, an earlier approximate method (Physics,7 260, 1936), and a more recent refinement (Bull. Math. Biophysics,10, 201, 1948) of the standard method are discussed.
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    Bulletin of mathematical biology 15 (1953), S. 121-141 
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    Notes: Abstract It is shown on the basis of (1) conservation of mass, (2) positive concentrations, and (3) the principle of detail balancing that periodic reactions cannot occur in a closed system described bylinear differential equations. The matrix,A, of the rate equations must be such that |A|=0,a ij〉0 fori≠j,a ii〈0, andVAV −1=B, whereV is diagonal andB is symmetric. These properties ofA imply that the latent roots are real and non-positive and that neither catalysis nor inhibition can be described bylinear equations. It is further shown that periodic reactions cannot occur in anopen system for which the matrix associated with the chemical reactions has the above properties and in which thesimple law of diffusion is obeyed. The relation of these results to Onsager's reciprocal relations and to previous work on periodic and cyclic chemical reactions is discussed. The utility of certain of these results for the treatment of isotope kinetics is indicated.
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    Bulletin of mathematical biology 15 (1953), S. 149-152 
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    Notes: Abstract It is demonstrated that an explanation of the small radius effect or the so-called sigma phenomenon may be obtained by noting that one of the effects of the presence of suspended particles in a flowing fluid is to increase the velocity of flow near the wall over that existing in the absence of particles. This effect may be considered equivalent to relaxing the boundary conditions at the wall. An expression for the viscosity is compared with data and fit is found to be good.
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    Bulletin of mathematical biology 15 (1953), S. 153-159 
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    Notes: Abstract The solution for the spatial distribution of ions in a Donnan equilibrium has been given by J. H. Bartlett and R. A. Kromhout (1952). The present note gives an explicit solution for the case in which the length of the region containing the membrane is large; in biological situations this requires only that the length considered should be greater than a few hundred Ångstrom units. The Donnan equilibrium may be considered to be a special case of a situation in which forces other than electrical act upon the ions; in particular, it represents the case in which only one ion is acted upon and the energy difference on the two sides of the membrane is infinite. An expression is given for the difference in energy of theith in terms of the electrical potential and of the ion concentrations. As an illustration, the results are applied to nerve membrane potentials.
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    Bulletin of mathematical biology 15 (1953), S. 161-165 
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    Notes: Abstract A mechanism is described which accounts for the active transport of Na+ ions through a membrane. It is assumed that at one side of the membrane the ion combines with a carrier ion, the resulting carrier compound then diffuses through the membrane and decomposes at the other side of the membrane. The free diffusion of the ions is also taken into account. The time rate of accumulation of the ion in question at the latter side of the membrane is calculated in terms of the concentrations of the ion at both sides of the membrane.
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    Bulletin of mathematical biology 15 (1953), S. 167-171 
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    Notes: Abstract The recent extension of the approximation method is applied to enable us to arrive at the time course of the concentrations at both sides of a membrane. From the differential equations which govern these, the steady-state solution is obtained in terms of the parameters, which are determined by the thickness of the diffusion layers, the chemical composition and reactions, and the diffusion constant of the membrane.
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    Bulletin of mathematical biology 15 (1953), S. 173-183 
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    Notes: Abstract An equation is derived from the spread of a “state” by contact through a thoroughly mixed population, in which the probability of transmission depends both on the over-all duration of the process and on the time an individual has been in the “state.” Cases in which this probability is a function of only one or the other of the two “times” are worked out. It is shown that in the case of dependence on “private time” alone the asymptotic value of the fraction of the population effected is the same as that derived by the random net approach.
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    Bulletin of mathematical biology 15 (1953), S. 235-235 
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    Bulletin of mathematical biology 15 (1953), S. 185-195 
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    Notes: Abstract The reflection of pressure waves in a fluid enclosed within a tube with an elastic wall is studied for the case of a localized change in diameter of the tube. The concept of impedance is introduced. The relation of the reflection characteristics of the parts of the tube at either side of the change is derived on the basis of the continuity of pressure and mass flow at the site of the change. This relations is used to derive the expression for the ratio of the pressure oscillations measured in front of, and behind, the constriction in terms of the constants of the system. As a result, a method is indicated to locate the coarctation from measurements of the pressures in front of, and behind it.
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    Notes: Abstract The question is raised concerning the possible causes of abnormally small standard deviations found in counting samples in which particles are distributed at random (e.g., blood cells, fat globules in milk, etc.). The effect of discarding abnormal samples is discounted inasmuch as small standard deviations occur even when all samples are counted. An approximation method is used to calculate the effect of finite particle size, of known repulsive forces between particles and of convection currents. This calculation shows that neither finite size nor the known repulsive forces are sufficient to account for the observed abnormality of standard deviation, but that convection currents can possibly account for it. The possible presence of long-range repulsive forces cannot, however, be excluded.
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    Bulletin of mathematical biology 15 (1953), S. 245-250 
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    Notes: Abstract The effect of finite particle size on the standard deviation in sample counts is computed for the one-dimensional case. To a first order of approximation the correction is found to be identifical with that found by H. de Vries (1953) using a general approximation method.
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    Bulletin of mathematical biology 15 (1953), S. 251-260 
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    Notes: Abstract A critical examination of the “classical” theories of photoreception in view of more recent experimental findings yields the result that these theories do not possess the property to describe all the more significant phenomena of photoreception correctly, and to some extent suffer the lack of more general applicability. The basis for a new and presumably more general theory of photoreception based on dynamical aspects is laid out. Emphasis is put on the time course of afferent and efferent excitation in the photoreception model, consisting of a receptor element, an afferent and an efferent neuron of the one-factor Rashevsky-type, and an effector organ.
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    Bulletin of mathematical biology 15 (1953), S. 197-234 
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    Notes: Abstract A mathematical model for the development of human society, beginning with the earliest stages of urban cultures, is outlined. In the early stages of history, behavior was characterized largely by adherence to a number of beliefs and prejudices of diffeirent kinds, which were accepted on faith and not subject to critical rational analysis. Due to psychobiological variability a very small number of individuals spontaneously appear at all times who challenge the accepted beliefs and prejudices and do not follow the accepted patterns of social behavior. The effect of these individuals upon the rest of the society, especially upon the younger generation, depends on the facilities with which information spreads in society. In earliest societies, when modern methods of mass communication were unknown, the channels of communication were practically identical with the channels of economic transport. The latter in its turn depended on the nature of the roads, and especially on the presence of waterway, which facilitated transportation. The sizes of the earliest cities and the distances between them were largely determined by relative ease of transporation. Expressions are derived for the average size of the earliest cities and for the average distance between them. The calculated average populations of the earliest cities are of the order of 103; the distance of the order of 102 km. Both are in agreement with some archaeological findings. An expression for the time spaon required for the development from the earliest stages of urban cultures to the present time is derived and shown to depend on the specific shoreline of the country, that is, the length of the shorline divided by the area of the country. It is pointed out that western Europe's specific shoreline, including land bordering both seas and rivers, is ten times as large as the shoreline area of other parts of the world. It is shown that this greater specific shoreline may account quantitatively for the faster social and technological development of western Europe in the last few centuries. The calculated total span of time of development from earliest urban cultures to our days is found to be of the order of magnitude of ten thousand years. It is shown that the model accounts for the existence at the present time of primitive cultures. A number of suggestions is made in regard to other possible applications of mathematics to history.
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    Bulletin of mathematical biology 15 (1953), S. 269-276 
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    Notes: Abstract The assumptions latent in the derivation of the integral equation of Branson are rendered explicit and discussed. It is shown that the equation is valid only for systems in which the substance disappears according to a linear rate law.
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    Bulletin of mathematical biology 15 (1953), S. 261-268 
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    Notes: Abstract It is shown that the validity of Branson's integral description of metabolizing systems is subject to severe limitations. The validity is insured only in cases where the reaction is of first order, or quasi of first order. In all other cases Branson's equation has to be modified to insure general applicability. The consequences of a different definition of the metabolizing functionF have also been investigated. With the new definitionF describes the pure effect of metabolization. It is found that in this case the integral equation is only capable of describing first-order reactions. With a slight modification of the integral equation it is possible to describe metabolites “with age”, which do not have reactions of definite order, but which satisfy the superposition principle.
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    Bulletin of mathematical biology 15 (1953), S. 277-292 
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    Notes: Abstract A problem in probability is stated with included the problem of the distribution of bacterial mutants as a special case. This problem is solved exactly but since the resulting expressions are too complicated for practical use, various approximate expressions for the distribution are considered, especially for the bacterial mutation case.
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    Bulletin of mathematical biology 15 (1953), S. 293-300 
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    Notes: Abstract Simple reaction and discrimination reaction, under the influence of imitation, are considered for the situation in which the stimulus or the stimuli vary slowly with time. The result is analogous to hysteresis under certain conditions. The calculations are facilitated by the solution of $$x = \int_{ - \infty }^{a + \beta x} {g\left( \xi \right)d} \xi ,$$ g(ξ) being the normal error function. Values ofx(α, β) are given in a table.
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    Bulletin of mathematical biology 15 (1953), S. 301-309 
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    Notes: Abstract On the basis of simple physical considerations the blood flow in a branching circulatory system is studied. The case of two groups of parallel vessels is treated. The vessels of the same group are supposed to be identical. The resistance of each group is determined by the resistance of each vessel in the group and by the number of vessels in the group. From the dependence of the resistance of each vessel on its radius an expression is obtained for the blood flow through each group of vessels in terms of the numbers and sizes of the vessels in each group. The number of open vessels in an organ and the radius of each of those vessels are assumed to depend on the metabolic rate of that organ. The relations so obtained, together with the expression above, are applied to derive the blood flow through an organ as a function of the metabolic rate of that organ. It is indicated that the relations obtained might describe the shifting of blood from one organ to another if the activity of one of them changes. A way is pointed out to treat neural regulation of this phenomenon.
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    Bulletin of mathematical biology 15 (1953), S. 361-365 
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    Notes: Abstract A stochastic model of population growth is treated using the Bellman-Harris theory of agedependent stochastic branching processes. The probability distribution for the population size at any time and the expectation are obtained when it is assumed that there is probability (1−σ), 0≤σ〈1, of the organism dividing into two at the end of its lifetime, and probability σ that division will not take place.
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    Bulletin of mathematical biology 15 (1953), S. 339-359 
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    Notes: Abstract In a previous paper, in which a possible mathematical approach to history was outlined, it was shown that urbanization plays an important part in the propagation of new ideas. The rate of such propagation influences the rate of historical developments. The present paper deals in more detail with possible mechanisms of formation of earliest cities. Equations are derived which give the limiting size of such cities and their rate of growth. Of particular importance for the spread of new ideas is the spread of information. The latter largely depends on the fraction of individuals who travel between city and country. Expressions for this quantity are derived. An approach is outlined to the mathematical study of the earliest social classes, which may have been formed as a result of military, religious, or economic stratifications.
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    Bulletin of mathematical biology 15 (1953), S. 395-409 
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    Notes: Abstract The velocity of propagation of a disturbance wave in a liquid flowing in a distensible tube is computed. The mathematical model is more general than those used in previous analyses: the tube wall properties are realistic; the convective part of the axial inertia forces is taken into account; radial inertia forces of both the fluid and tube wall are present; viscous stresses are present. Four parameters influencing the velocity of propagation are obtained and discussed. Curves are plotted illustrating the effects of the parameters. Contrary to the results of previous analyses, viscous effects are shown to be appreciable in blood flow. It is also shown that radial inertia effects can be important in laboratory set-ups.
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    Bulletin of mathematical biology 15 (1953), S. 411-429 
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    Notes: Abstract A general theory of the drying of frozen tissue is developed and applied to the measurement of the drying rate of frozen guinea pig liver. It is shown that for a given temperature of the subliming ice crystals the mininum drying time of a piece of guinea pig liver is greater than the minimum sublimation time of a piece of ice of the same size and shape by a factor of the order of one thousand. This fact has many implications in the design of freeze-dry apparatus which will be developed in a following paper.
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    Bulletin of mathematical biology 15 (1953), S. 477-488 
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    Notes: Abstract The equations governing the time course of the exchange of substances between the blood in the capillaries and the extracellular space are solved for the case of substances which do not penetrate the cells. The equations given relate the time course of the exchange process to the various tissue and circulation parameters such as the specific capillary wall area, the pore area, the inter-capillary distance, the size of the extra-vascular, extra-cellular space, the diffusion coefficient in this space, and the velocity of blood in the capillaries. Some experimental work on capillary exchange is discussed in relation to the theory and estimates are made of the relative importance of the various tissue and circulation parameters in the exchange of substances in different tissues.
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    Bulletin of mathematical biology 52 (1990), S. 455-475 
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    Notes: Abstract Random clone mapping of genomic DNA is a subject of great interest in molecular biology.E. coli has just been mapped and work is progressing on some human chromosomes. In this paper we give estimates of the fraction of genomic DNA which is not clonable by partial digest with a restriction enzyme.
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    Bulletin of mathematical biology 52 (1990), S. 483-484 
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    Bulletin of mathematical biology 52 (1990), S. I 
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    The Geneva risk and insurance review 15 (1990), S. 5-16 
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    Topics: Economics
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    The Geneva risk and insurance review 15 (1990), S. 73-79 
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    Notes: Abstract When assets are nominal, non-informative rational expectations equilibria exist.
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    Notes: Abstract Previous work (Macey, 1952) in the application of the one-factor theory to the heart is extended. The rate of production of the excitatory state is assumed to be linear. Two possible mechanisms are indicated whereby such a situation might arise. Assumptions are made regarding the mode of action of the chemical mediators on the heart, and an equation is derived relating the heart rate to the frequency of nerve impulses traveling along the cardiac nerves. This result compares favorably with the experimental findings of A. Rosenblueth and F. A. Simeone (1934). Other experimental results are interpreted in terms of the theory.
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    Bulletin of mathematical biology 15 (1953), S. 561-563 
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    Bulletin of mathematical biology 52 (1990), S. 1-1 
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    Bulletin of mathematical biology 52 (1990), S. 3-23 
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    Bulletin of mathematical biology 52 (1990), S. 25-71 
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    Notes: Abstract This article concludes a series of papers concerned with the flow of electric current through the surface membrane of a giant nerve fibre (Hodgkinet al., 1952,J. Physiol. 116, 424–448; Hodgkin and Huxley, 1952,J. Physiol. 116, 449–566). Its general object is to discuss the results of the preceding papers (Section 1), to put them into mathematical form (Section 2) and to show that they will account for conduction and excitation in quantitative terms (Sections 3–6).
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    Bulletin of mathematical biology 52 (1990), S. 73-97 
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    Notes: Abstract The McCulloch-Pitts paper “A Logical Calculus of the Ideas Immanent in Nervous Activity” was published in theBulletin of Mathematical Biophysics in 1943, a decade before the work of Hodgkin, Huxley, Katz and Eccles. The McCulloch-Pitts neuron is an extremely simplified representation of neural properties, based simply on the existence of a threshold for the activation of an action potential.
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    Bulletin of mathematical biology 52 (1990), S. 99-115 
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    Notes: Abstract Because of the “all-or-none” character of nervous activity, neural events and the relations among them can be treated by means of propositional logic. It is found that the behavior of every net can be described in these terms, with the addition of more complicated logical means for nets containing circles; and that for any logical expression satisfying certain conditions, one can find a net behaving in the fashion it describes. It is shown that many particular choices among possible neurophysiological assumptions are equivalent, in the sense that for every net behaving under one assumption, there exists another net which behaves under the other and gives the same results, although perhaps not in the same time. Various applications of the calculus are discussed.
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    Bulletin of mathematical biology 52 (1990), S. 199-207 
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    Bulletin of mathematical biology 52 (1990), S. 117-152 
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    Notes: Abstract The evolution of spatial pattern is a central issue in developmental biology. Turing's (Phil. Trans. R. Soc. Lond. B237, 37–72, 1952) chemical theory of morphogenesis is a seminal contribution. In this talk I give a personal and necessarily limited view of its impact on mathematical and developmental biology. I briefly describe some of the interesting mathematical aspects of Turing's reaction-diffusion mechanism and discuss some of the different models which Turing's vision inspired. The emphasis throughout is on the practical biological applications of the various theories.
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    Bulletin of mathematical biology 52 (1990), S. 209-240 
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    Notes: Abstract Mathematical expressions are found for the effect of selection on simple Mendelian populations mating at random. Selection of a given intensity is most effective when amphimixis does not affect the character selected, e.g. in complete inbreeding or homogamy. Selection is very ineffective on autosomal recessive characters so long as they are rare.
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    Bulletin of mathematical biology 52 (1990), S. 241-295 
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    Bulletin of mathematical biology 52 (1990), S. 297-318 
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    Bulletin of mathematical biology 52 (1990), S. 359-373 
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    Notes: Abstract A new algorithm for optimal sequence alignment allowing for long insertions and deletions is developed. The algorithm requires O((L+C)MN) computational steps, O(LN) primary memory and O(MN) secondary memory storage, whereM andN(M≥N) are sequence lengths,L (typicallyL≤3) is the number of segment specifying the gap weighting function, andC is a constant. We have also modified our earlier traceback algorithm so that it finds all and only the optimal alignments in a compact form of a directed graph. The current versions accept a set of aligned sequences as input, which facilitates multiple sequence alignment by some iterative procedures.
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    Bulletin of mathematical biology 52 (1990), S. 397-429 
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    Notes: Abstract The kinetic model of cortical-like neural systems is amplified with elements related to a gross lamination in three parts of the basic system. A reduced version of the model, aiming to study only short-range, random aspects of activity propagation, was subjected to an intensive computational experimentation, and the results are briefly presented. The comparison of these results with those of a previous paper, in which aspects related mainly to long-distance effects were described, suggested the possibility of extending the model by considering new features related to phenomena of attention. The results of experimentations with the whole model revealed the possibility of laying the bases for a description of the cognitive activity in a neural frame.
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    Bulletin of mathematical biology 52 (1990), S. 431-453 
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    Notes: Abstract A method of inductive inference known asminimum message length encoding is applied to string comparison in molecular biology. The question of whether or not two strings are related and, if so, of how they are related and the problem of finding a good theory of string mutation are treated as inductive inference problems. The method allows the posterior odds-ratio of two string alignments or of two models of string mutation to be computed. The connection between models of mutation and existing string alignment algorithms is made explicit. A fast minimum message length alignment algorithm is also described.
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    Bulletin of mathematical biology 52 (1990), S. 477-482 
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