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  • Springer  (101,032)
  • 2005-2009
  • 1990-1994  (58,868)
  • 1980-1984  (42,164)
  • 1925-1929
  • 1990  (58,868)
  • 1980  (42,164)
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  • 2005-2009
  • 1990-1994  (58,868)
  • 1980-1984  (42,164)
  • 1925-1929
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  • 1
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    Bulletin of mathematical biology 42 (1980), S. 131-135 
    ISSN: 1522-9602
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract The theory of complementary variational principles is used to obtain maximum and minimum principles for diffusion problems with Michaelis-Menten kinetics. In an illustrative calculation we obtain an extremely accurate variational solution in good agreement with the numerical solution of McElwain (1978).
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  • 2
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    Bulletin of mathematical biology 42 (1980), S. 137-141 
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  • 3
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    Bulletin of mathematical biology 42 (1980), S. 181-189 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract Necessary and sufficient conditions for primitivity of a product of two Leslie matrices are given. Such a product could be used in modeling the growth of a population governed alternately by two different sets of fertility and survival parameters.
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  • 4
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    Bulletin of mathematical biology 42 (1980), S. 173-180 
    ISSN: 1522-9602
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    Notes: Abstract Zadeh's transfer function method for linear time-variable systems is used to apply frequency-domain analysis to a periodically time-varying elastance model of the left ventricle. Left ventricular pressure computed from the system function of the time-varying elastance and the phasors of aortic flow shows a typical waveform of the measured ventricular pressure.
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    Bulletin of mathematical biology 42 (1980), S. 901-901 
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  • 6
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    Bulletin of mathematical biology 52 (1990), S. 153-197 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    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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  • 8
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    Bulletin of mathematical biology 52 (1990), S. 335-337 
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  • 9
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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 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    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 
    ISSN: 1522-9602
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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 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    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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  • 18
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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 
    ISSN: 1531-5878
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    Topics: Electrical Engineering, Measurement and Control Technology
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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 
    ISSN: 1531-5878
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    Topics: Electrical Engineering, Measurement and Control Technology
    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 
    ISSN: 1531-5878
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    Topics: Electrical Engineering, Measurement and Control Technology
    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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    Topics: Electrical Engineering, Measurement and Control Technology
    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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    Topics: Electrical Engineering, Measurement and Control Technology
    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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    Topics: Electrical Engineering, Measurement and Control Technology
    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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    Topics: Electrical Engineering, Measurement and Control Technology
    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 42 (1980), S. 147-160 
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    Notes: Abstract A theory of noise fluctuations is developed which is applicable to systems of any size in which unimolecular or bimolecular reactions are occurring. The main difference between small and large reacting systems is that in the former the probability of finding a particle in a particular state does not obey a Gaussian distribution, but satisfies a distribution which reflects the mechanism of the chemical reaction. This difference is reflected in the main result of the theory: an autocorrelation function that is expressible as a sum of exponentials, the amplitudes of which are explicit functions of the moments of the distribution. Thus, by using small systems, the autocorrelation function,in principle, allows the elucidation of reaction mechanisms. Numerical simulations indicate that for reacting systems having ten or fewer particles, the deviation of the autocorrelation function from a single exponential should be easily detectable, and that estimates of the first four moments of the distribution should be possible. Accurate inference of the distribution, however, will require further mathematical and experimental advances.
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    Bulletin of mathematical biology 42 (1980), S. 161-172 
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    Notes: Abstract The recent mathematical formalization of the concepts of matter and extrinsical energy, which are used for the relational representation of biological systems, is employed in the analysis of the important experimental discoveries of Comorosanet al. related to low energy electromagnetic irradiations on enzyme substrates. By means of the present analysis one of the properties inherent to the experimental phenomena is more precisely exposed, and theoretical developments corresponding to “energetical evolutions” in a biological system (Leguizamón, 1976) may now have an experimental basis. Important limitations are introduced for the validity of the commutativity and associativity of cartesian product of sets, when they represent matter and its linked extrinsical energy. In connection with this last aspect, new important knowledge is obtained for the relational mathematical representation of biological systems.
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    Bulletin of mathematical biology 42 (1980), S. 397-429 
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    Notes: Abstract The structure of solutions to a simple spatially dependent population model involving growth and death is investigated. Two forms of motility of the population are considered: (1) random motion only modeled by a Fickian law, and (2) a directed component of motion (chemotaxis), included in addition to the random motion. Under certain growth conditions a traveling wave of constant speed is approached. This speed can be increased by the addition of the chemotaxis with a corresponding increase in the asymptotic population. Development of initial conditions into a wave is illustrated numerically.
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    Bulletin of mathematical biology 42 (1980), S. 365-396 
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    Notes: Abstract This paper describes mechanisms of intracellular and intercellular adaptation that are due to spatial or temporal factors. The spatial mechanisms support self-regulating pattern formation that is capable of directing self-organization in a large class of systems, including examples of directed intercellular growth, transmitter production, and intracellular conductance changes. A balance between intracellular flows and counterflows causes adaptation. This balance can be shifted by environmental inputs. The decrease in Ca2+-modulated outward K+ conductance in certain molluscan nerve cells is a likely example. Examples wherein Ca2+ acts as a second messenger that shunts receptor sensitivity can also be discussed from this perspective. The systems differ in basic ways from recent diffusion models. Chemical transducers driven by membrane-bound intracellular signals can establish long-range intercellular interactions that compensate for variable intercellular distances and are invariant under developmental size changes; diffusional signals do not. The intracellular adaptational mechanisms are formally analogous to intercellular mechanisms that include cellular properties which are omitted in recent reaction-diffusion models of pattern formation. The cellular models use these properties to compute size-invariant properties despite wide variations in their intercellular signals. Mechanisms of temporal adaptation can be derived from the simplest laws of chemical transduction by using a correspondence principle. These mechanisms lead to such properties of intercellular signals as transient overshoot, antagonistic rebound, and an inverted U in sensitivity as intracellular signals or adaptation levels shift. Such effects are implicated in studies of behavioral, reinforcement, motor control, and cognitive coding.
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    Bulletin of mathematical biology 42 (1980), S. 447-459 
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    Notes: Abstract Large radiation doses to the lung can cause early death from cardiopulmonary insufficiency resulting from radiation pneumonitis and pulmonary fibrosis. A model for early death following inhalation of insoluble radioactive particles is propose. The model is based on three assumptions: (1) early death results from damage to a cluster of cells from a large number of cell clusters at risk, (2) the dose that causes early death depends on how the radiation is delivered in time and (3) the cell clusters at risk to damage are equally sensitive ro radiation. Results from asymptotic theory of extreme values, along with biophysical considerations, suggest that the cumultive distribution function for the absorbed radiation dose to the production of pulmonary injury sufficient to cause early death is best estimated by the third asymptotic distribution without a threshold. This distribution function is identical to the Weibull cumulative distribution function. Data for Beagle dogs after inhaling relatively insoluble forms of alpha- or beta-gamma-emitting particles are shown to support the Weibull model.
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    Bulletin of mathematical biology 42 (1980), S. 461-480 
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    Notes: Abstract Models of the human respiratory tract were developed based on detailed morphometric measurements of a silicone rubber cast of the human tracheobronchial airways. Emphasis was placed on the “Typical Path Lung Model” which used one typical pathway to represent a portion of the lung, such as a lobe, or to represent the whole lung. The models contain geometrical parameters, including airway segment diameters, lengths, branching angles and angles of inclination to gravity, which are needed for estimating inhaled particle deposition. Aerosol depositions for various breathing patterns and particle sizes were calculated using these lung models and the modified Findeisen-Landahl computational scheme. The results agree reasonably well with recent experimental data. Regional deposition, including lobar deposition fractions, are also calculated and compared with results based on the ICRP lung deposition model.
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    Bulletin of mathematical biology 42 (1980), S. 481-488 
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    Notes: Abstract The completely symmetrical system is defined as having identical transfer coefficients between pairs of compartments and the same loss coefficient for each compartment. The eigenvalues and eigenvector are explicitly found along with the inverses of the system matrix and the matrix of eigenvectors. Many properties, special instances of more general theorems, can be seen at once from the explicit analytic solution of the initial value, washout and washin problems. The system serves as a known case for testing estimation procedures, algorithms for solutions of linear systems, eigenvalue-eigenvector and inversion routines and is of considerable tutorial value.
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    Bulletin of mathematical biology 42 (1980), S. 431-446 
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    Notes: Abstract The mathematical structures underlying the theories of organismic sets, (M, R)-systems and molecular sets are shown to be transformed naturally within the theory of categories and functors. Their natural transformations allow the comparison of distinct entities, as well as the modelling of dynamics in “organismic” structures.
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    Bulletin of mathematical biology 42 (1980), S. 489-505 
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    Notes: Abstract To explain the sodium conductance change using Wei's dipole model (Wei, 1969), we may expect that during depolarization the dipole's population difference, ΔN, is first reduced and then returns more slowly to its resting value. This paper shows that the experimental results of gating currents support this idea. Such time course of ΔN, however, is not a usual relaxation process. To account for the unusual behavior of ΔN, we propose two additional assumptions: (1) there exists a special coupling system (probably the intramolecular vibrations) whose coupling strength with the dipoles is much stronger than with the thermal bath (intermolecular vibrations), and (2) there also exist “traps” for the dipole's excitation energy so that this energy is transformed into other energy forms at a rate increasing with the increase of depolarization. Experiments suggest that the traps are proteins located at the inner membrane surface.
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    Bulletin of mathematical biology 42 (1980), S. 507-528 
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    Notes: Abstract Current research into the dynamics of iterative ecological and biological models has lead to a number of theorems concerning the existence of various types of iterative dynamical behavior. In particular, much study has been done on the dynamical behavior of the “simplest dynamical system”f b(x)=bx(1−x), which is just the canonical discrete form of logistic growth equations found in ecology, sociobiology, and population biology. In this paper, we make use of some of the techniques and concepts of topological dynamics to construct a number of generalized conjugacy theorems. These theorems are then used to demonstrate that the mappingf b has a number of conjugacy classes in which the dynamics of the iterates is equivalent to within a change of variables. The concepts of fitness and survival in logistic equations are then shown to be independent, if we follow certain intuitive definitions for these concepts. This conclusion follows from a comparison of the conjugacy classes of the functionf b and the extinction sets off b.
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    Notes: Abstract For chemical reactions not at equilibrium but proceeding in the forward direction in the steady state, a result found by a method first introduced by H. G. Britton (1963, 1965) is generalized to prove that if $${{\vec J} \mathord{\left/ {\vphantom {{\vec J} {\overset{\lower0.5em\hbox{$\smash{\scriptscriptstyle\leftarrow}$}}{J} }}} \right. \kern-\nulldelimiterspace} {\overset{\lower0.5em\hbox{$\smash{\scriptscriptstyle\leftarrow}$}}{J} }}$$ is the unidirectional flux ratio, $${{\vec J} \mathord{\left/ {\vphantom {{\vec J} {\overset{\lower0.5em\hbox{$\smash{\scriptscriptstyle\leftarrow}$}}{J} }}} \right. \kern-\nulldelimiterspace} {\overset{\lower0.5em\hbox{$\smash{\scriptscriptstyle\leftarrow}$}}{J} }}$$ exp (−ΔG/RT). The conditions under which the equality or inequality applies are discussed. If the unidirectional fluxes are not in the steady state, the unidirectional flux ratio is time invariant in certain specific situations. One such important case is for chemical reaction systems with an ordered sequence of reactions. For systems with more than one pathway, $${{\vec J} \mathord{\left/ {\vphantom {{\vec J} {\overset{\lower0.5em\hbox{$\smash{\scriptscriptstyle\leftarrow}$}}{J} }}} \right. \kern-\nulldelimiterspace} {\overset{\lower0.5em\hbox{$\smash{\scriptscriptstyle\leftarrow}$}}{J} }}$$ is not constant except for special cases. These results also apply to diffusional and active transport systems.
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    Bulletin of mathematical biology 42 (1980), S. 599-600 
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    Bulletin of mathematical biology 42 (1980), S. 539-549 
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    Bulletin of mathematical biology 42 (1980), S. 551-597 
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    Notes: Abstract The nonlinear second-order difference equationx n+1=axn(1-xn−1), where 0≦x nX≦1 anda ≧1, is examined from varying points of view, analytical, numerical and geometrical. An analytic expression is obtained for an invariant attracting curveC ∞ (a) in phase space, which becomes the central object of study. This basic curve, which replaces the simple parabolic shape typical of many analogous first-order models, may have a complicated geometrical structure. As the parametera increases,C ∞(a) undergoes transformations characterized by the dynamical descriptions: stable node→stable focus→stable limit cycle →chaotic attractor. Although the limited characterization ofchaos by the appearance of nonperiodic solutions and solutions of arbitrarily large period is relied upon, this appears to be only a simplified approximation of the real behavior of solutions. Trajectories (x n, xn+1),n=0,1,…, are calculated using the related nonlinear planar mapT a(x,y)=(y,ay(1−x)), and regions of persistence and escape are described for characteristic values ofa. The study of persistence, of even more fundamental interest than the associated problems of periodicity and stability, receives special attention. We introduce a geometrical model, similar in many respects to that for the well-known analoguex n+1=axn(1−x n), but having several new and important features. It appears that as the parametera increases in the chaotic regime there are infinitely many intermittent bursts of increase in the probability that any initial point (x 0, x1) will persist in the unit square under successive iterations of the mappingT a, an unexpected property that should be of interest for applications. A discussion of the applicability of these results to population dynamics theory is given, and it is suggested that such equations might find useful application to problems in developmental biology as well.
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    Bulletin of mathematical biology 42 (1980), S. 627-645 
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    Notes: Abstract Based on the principle of minimum power, a mathematical model of the functional state of the oxygen transport system is presented. The optimization model minimizes the power expenditure of the heart, bone marrow, lung and other tissues. The model is used to determine the functional parameters of the oxygen transport system in man under both normal and varying barometric pressures. Theoretical results are compared with experimental data.
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    Bulletin of mathematical biology 42 (1980), S. 601-625 
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    Notes: Abstract A quantitative model of ion binding and molecular interactions in the lipid bilayer membrane is proposed and found to be useful in examining the factors underlying such membrane characteristics as shape, sidedness, stability and vesicle size at various cation concentrations. The lipid membrane behaves as a bilayer couple whose preferential radius of curvature depends on the expansion or contraction of one monolayer relative to the other. It is proposed that molecular packing may be altered by electrostatic repulsion of adjacent like-charged phospholipid headgroups, or by bringing two headgroups closer together by divalent cation crossbridging. The surface concentrations of each type of cation-phospholipid complex can be described by simple binding equilibria and the Gouy-Chapman-Stern formulation for the surface potential in a diffuse double layer. The asymmetric distribution of acidic phospholipids in most biological membranes can account for the differential effects of identical ionic environments on either side of the bilayer. The fraction of vesicle material which tends to have a right-side-out orientation may be approximated by a normal distribution about the mean curvature. The theory generates vesicle sidedness distributions that, when fitted to experimental results from human erythrocyte membranes, provide an alternative method of estimating intrinsic cationphospholipid dissociation constants and other molecular parameters of the bilayer. The results also corroborate earlier suggestions that the Gouy-Chapman theory tends to overestimate free counter-ion concentrations at the surface under large surface potentials.
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    Bulletin of mathematical biology 42 (1980), S. 681-689 
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    Notes: Abstract The “yellow strips” on the cuticle of the Oriental Hornet (Vespa orientalis, Hymenoptera, Vespinae), present photoelectric properties. A mathematical model for the relative changes in resistance as a photoconductive process conforms to the general model for a semiconductor with traps.
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    Bulletin of mathematical biology 42 (1980), S. 701-718 
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    Notes: Abstract Damped nonlinear oscillations in biological and biochemical systems are investigated by the extended Krylov-Bogoliubov-Mitropolskii (KBM) method. A review on the extension made by Popov to the KBM method is given and also further improvements are presented. Applications are made to models of oscillating chemical reactions (Lefever and Nicolis, 1971), FitzHugh (1961) equations, and population dynamics (Gatto and Rinaldi, 1977). Comparison to damped oscillating physical and engineering systems is made.
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    Bulletin of mathematical biology 42 (1980), S. 719-728 
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    Notes: Abstract The conditions that will allow the lumping together of several age classes in the Leslie model are investigated. We show that if the lumping is to be valid for all population distributions, then the parameters of the model must be periodic. Lumping is valid when the population is in equilibrium, but equilibrium should be tested before the model is lumped.
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    Bulletin of mathematical biology 42 (1980), S. 647-679 
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    Notes: Abstract Catastrophe theory is a mathematical theory which, allied with a new and controversial methodology, has claimed wide application, particularly in the biological and the social sciences. These claims have recently been heatedly opposed. This article describes the debate and assesses the merits of the different arguments advanced.
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    Bulletin of mathematical biology 42 (1980), S. 765-795 
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    Notes: Abstract Estimates of capillary tracer permeability calculated using multiple indicator data depend upon the particular model adopted to describe blood tissue exchange. The model proposed by Crone (1963) is appropriate when some of the injected tracer diffuses into the tissue but does not return appreciably to the bloodstream before data collection is terminated. Under these conditions extraction of tracer by the tissue depends on a single dimensionless parameter, αcap, defined as the ratio of capillary permeability surface area to water flow. The effects of finite red cell tracer permeability on the Crone model estimate of capillary permeability are examined in the present study. The results indicate that even when back diffusion from the extravascular space is negligible, significant errors in the Crone model estimate can be expected when capillary permeability is relatively high and the ratio of red cell to capillary permeability is less than unity. However, when an aliquot of blood is equilibrated with tracer prior to injection and the dimensionless capillary permeability is relatively low (i.e. αcap ≦ 0.25 for a haematocrit≦50%), the whole blood Crone model estimate of αcap will be within 10% of the actual value, irrespective of red cell permeability. Red cell-plasma exchange for commonly used tracer-organ combinations should not significantly affect Crone estimates of capillary permeability under normal physiological conditions, but may be important in low flow situations.
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    Bulletin of mathematical biology 42 (1980), S. 807-828 
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    Notes: Abstract Assuming truncated ellipsoidal geometry for the right and left ventricles, a model is developed for the myocardium enabling biventricular mechanical behavior to be studied. Employing pressure-volume data taken from normal dog hearts and from hearts in which the pulmonary artery has been banded over periods of 2–40 weeks, it is shown that: (a) right ventricular wall stresses are higher than left ventricular stresses; (b) right ventricular wall stress increases initially to a maximum after 3–4 weeks followed by a decline to normal and even subnormal levels, attaining a minimum value at 32–33 weeks; (c) left ventricular stresses behave in a similar manner, attaining their maximum and minimum levels after 7–8 weeks and 32–33 weeks respectively. These results suggest that surgical or medical therapy in patients with hypertrophied ventricles might be more appropriate during the period of wall stress reduction.
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    Bulletin of mathematical biology 42 (1980), S. 837-845 
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    Notes: Abstract In this paper we describe a mathematical model of the oscillations of the diaphragm which limits the vitreous body from the anterior segment of the human eye after the lens has been removed in a cataract operation. We study the motion of this diaphragm driven by movements of the eye. Firstly, a mathematical statement of the problem is given and then we solve the problem exactly for a given class of eye movements. From the analysis we deduce that significant oscillations of the membrane are driven by saccades and that it is the angular acceleration of the eye which causes these types of oscillations. A numerical example is given.
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    Bulletin of mathematical biology 42 (1980), S. 871-887 
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    Notes: Abstract The Lotka-Volterra system of prey-predator equations is considered with a special type of continuous time delay. In the case of equal diffusion coefficients Hopf’s bifurcation technique is used to show the existence of travelling wave train solutions for the prey-predator system.
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    Bulletin of mathematical biology 42 (1980), S. 861-870 
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    Notes: Abstract A mathematical model of prothrombin activation is being proposed which includes the feedback mechanism of thrombin and the alteration of factor V by thrombin. This model is in good agreement with experimental data for the dependence of the rate of thrombin formation on the concentrations of factors V and X a . In particular, it correctly predicts the existence and location of a maximum in both of these cases.
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    Bulletin of mathematical biology 42 (1980), S. 847-859 
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    Notes: Abstract A new model of the upper tracheobronchial tree is proposed to account for the three-dimensional nature of the airway system. In addition to the tube length, the tube diameter, and the branching angle, the model includes information on the orientation angle of each tube relative to its parent tube. The orientation angle, defined as the angle between two successive bifurcations, is useful for calculating the gravitational inclination of each tube. The information on orientation angle is further used to construct a binary coding system for identifying individual tubes in the airway tree. The proposed model is asymmetrical, but the same principles can be readily used to construct a symmetrical one.
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    Bulletin of mathematical biology 42 (1980), S. 889-897 
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    Notes: Abstract In any control system for which the number of independent controls is smaller than the number of degrees of freedom to be controlled, our choice of control in any state is restricted to a submanifold of smaller dimension than the tangent space. This simple fact has a number of important consequences for questions of biological import; we consider its implications for adaptation, for senescent phenomena and for the determination of tertiary structures of polypeptides through control of certain average properties. We also formulate the Pontryagin Maximum Principle of Optimal control theory in such a way as to inquire whether specific biodynamic systems can be regarded as optimal with respect to rate of accumulation of particular quantities of the system. We find that if this is possible, the quantity in question must play the role of a clock.
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    Bulletin of mathematical biology 42 (1980), S. 899-900 
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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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    Bulletin of mathematical biology 42 (1980), S. 1-15 
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    Notes: Abstract A computational model to predict deposition of a wide variety of particulate pollutants in several species of mammals is presented. The model incorporates breathing pattern and detailed anatomical models of the respiratory tract based on extensive morphometric measurements of individual airways. The predicted deposition from this general model is in close agreement with observed deposition of monodisperse aerosols in rats. Particle size and density and respiratory breathing patterns are the critical parameters affecting regional deposition.
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    Bulletin of mathematical biology 42 (1980), S. 17-36 
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    Notes: Abstract A theory of antigen-antibody induced particulate aggregation is developed by investigating the stability of model systems of particles. Conditions for the formation of large aggregates are derived by imposing the requirement that at equilibrium a statistically significant number of redundant bonds would occur in a reduced monomer-dimer model system. A relationship is obtained which predicts the fractional agglutination in the reduced dimer system as a function of the antigen, antibody and particulate concentrations: $$\frac{g}{{2f c_0 (1 - g)^{2^ - } }} = \frac{{s_1 }}{r} + \frac{{s_1 s_2 }}{{2!r^2 }} + ... + \frac{{s_1 s_2 ...s_j }}{{j!r^j }},$$ wherec 0 is the initial concentration of monomer,f is a proximity factor,g is the fractional agglutination,s i is the average rate of formation of theith bond from an (i−1)th bound dimer, andr is the average rate of dissociation of a single antibody-antigen bond.
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    Bulletin of mathematical biology 42 (1980), S. 37-56 
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    Notes: Abstract The roles of the concentrations of the three interacting constituents in the aggregation process (antibodies, antigens and particulates) are analyzed in detail. It is shown that the basic equation derived in Part I is consistent over a broad range of conditions with experimental findings previously reported.
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    Bulletin of mathematical biology 42 (1980), S. 57-78 
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    Notes: Abstract A general mathematical model describing the biochemical interactions of the hormones luteinizing hormone releasing hormone (LHRH), luteinizing hormone (LH) and testosterone (T) in the male is presented. The model structure consists of a negative feedback system of three ordinary differential equations, in which the qualitative behavior is either a stable constant equilibrium solution or oscillatory solutions. A specific realization of the model is used to describe the experimental observations of pulsatile hormone release, its experimental suppression, the onset of puberty, the effects of castration, and several other qualitative and quantitative results. This model is presented as a first step in understanding the physicochemical interactions of the hypothalamic-pituitary-gonadal axis.
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    Bulletin of mathematical biology 42 (1980), S. 79-94 
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    Notes: Abstract Based upon the transition rate equation of dipoles in the membrane, we deal with two important aspects of interaction of nerve signals: (1) conditions for nerve excitation and (2) frequency spectrum analysis of nerve impulse. Interrelations between signal amplitudes and frequencies are formulated in detail. There are several important conclusions which can be drawn from our calculations. First, toexcite the nerve, low frequencies are generally more effective than high frequencies. Second, tosedate the nerve (i.e. to suppress undesired activities), high frequencies would suit better. Third, harmonics produced through interactions of nerve signals are not necessarily weaker than the fundamental frequencies. The great significance of our theory is that it indicates in principle the feasibility to alter or rewrite the information contents of a nerve message in our body by applying stimulations of appropriate strengths and frequencies. Thus, the theory provides a physical basis and hence some understanding for a new branch of medicine—neuro therapy such as Nogier's auriculotherapy, Lamy's phonophoresis, Voll's electroacupuncture and the fast rising TENS (transcutaneous electro-neuro stimulation).
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    Bulletin of mathematical biology 42 (1980), S. 107-117 
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    Notes: Abstract A new physical property, called resonance of the B-type is hypothetically attached to the λ =546 nm irradiated crystalline (small) molecules. In this respect an up or down configuration is assumed for those states obtained through irradiation times that are multiples of 5 sec. With these assumptions, the cellular receptors that may detect these states appear to belong to three classes: the up, down and alternatively mixed up-down. Using the classic formalism of eigenvectors and eigenvalues, a simple spectroscopic type of formula is derived, through which all the possible states of the above characteristic may be obtained.
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    Bulletin of mathematical biology 42 (1980), S. 119-130 
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    Notes: Abstract A model of ecosystems with migration is proposed from the viewpoint of flow. This model explains the following two points: (1) How the density-dependent terms in population dynamics arise as a consequence of migration. (2) How the ecosystem exhibits a hierarchy in energy per unit biomass.
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    Bulletin of mathematical biology 42 (1980), S. 143-145 
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    Bulletin of mathematical biology 42 (1980), S. 95-106 
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    Notes: Abstract For precise boundary conditions of biological relevance, it is proved that the steadily propagating plane-wave solution to the Fisher equation requires the unique (eigenvalue) velocity of advance 2(Df)1/2, whereD is the diffusivity of the mutant species andf is the frequency of selection in favor of the mutant. This rigorous result shows that a so-called “wrong equation”, i.e. one which differs from Fisher's by a term that is seemingly inconsequential for certain initial conditions, cannot be employed readily to obtain approximate solutions to Fisher's, for the two equations will often have qualitatively different manifolds of exact solutions. It is noted that the Fisher equation itself may be inappropriate in certain biological contexts owing to the manifest instability of the lowerconcentration uniform equilibrium state (UES). Depicting the persistence of a mutantdeficient spatial pocket, an exact steady-state solution to the Fisher equation is presented. As an alternative and perhaps more faithful model equation for the propagation of certain species properties through a homogeneous population, we consider a reaction-diffusion equation that features a cubic-polynomial rate expression in the species concentration, with two stable UES and one intermediate unstable UES. This equation admits a remarkably simple exact analytical solution to the steadily propagating plane-wave eigenvalue problem. In the latter solution, the sign of the eigenvelocity is such that the wave propagates to yield the “preferred” stable UES (namely, the one further removed from the unstable intermediate UES) at all spatial points ast→∞. The cubic-polynomial equation also admits an exact steady-state solution for a mutant-deficient or mutant-isolated spatial pocket. Finally, the perpetuating growth of a mutant population from an arbitrary localized initial distribution, a mathematical problem analogous to that for ignition in laminar flame theory, is studied by applying differential inequality analysis, and rigorous sufficient conditions for extinction are derived here.
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    Bulletin of mathematical biology 42 (1980), S. 191-220 
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    Notes: Abstract The binding of mono-, di- and trivalent cations to negatively charged surfaces is studied within the framework of a modified Gouy-Chapman equation. For any given combination of ions of the above valences, the existence and uniqueness of the solution for the surface potential is shown. The treatment provides the surface potential and charge density. For a system containing only monovalent and divalent ions, analytical solutions are given. When trivalent ions are also present, a procedure based on numerical integration is described. The distance dependence of the electrostatic potential for planar surfaces is given. The calculations provide the amount of cations tightly bound and the amount trapped in the double layer region. The competition between cations for binding to surfaces is elucidated.
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    Bulletin of mathematical biology 42 (1980), S. 221-238 
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    Notes: Abstract This paper deals with a model describing the behavior of barium-treatedApalysia neurons. The model is represented by a dynamical system, so-called “complete system”, defined in R4 and depending on a small parameter. The study of this system under zero membrane current conditions was performed with the use of the qualitative theory of singular perturbations. We show that this system has a stable periodic solution of the discontinuous type when the small parameter tends to 0+. A reduced system defined in R3, associated to the complete system was also studied: it corresponds to a constant activation of the inward current. We demonstrate that the corresponding hypothetical cell remains silent under zero current conditions.
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    Notes: Abstract In the study of chemical modification of enzymes and other biologically active proteins, plots of fractional residual activity as a function of number of groups modified per enzyme molecule are often used to establish a correlation between the chemical modification and enzyme inactivation reactions and to determine the stoichiometry of the modification reaction. This paper presents a critical examination of the underlying theoretical framework of such graphs. Whereas these plots are usually presented as linear functions, it is shown here that the general equation describing the relationship between inactivation and modification contains an exponential term; therefore, in the general case, the plot is actually a curve. It is suggested that caution be exercised in the interpretation of such plots and that equations such as those derived in the text be used to fit theoretical curves to the data, in order to maximize the information gained from chemical modification experiments.
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    Bulletin of mathematical biology 42 (1980), S. 257-265 
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    Notes: Abstract This communiction argues that so-called “hermaphroditic” tracer systems, which are neither open nor closed, do not exist physically. The argument is based on the assumption that any observable (possibly nonhomogeneous) macroscopic compartment can be approximated by a compartmentC with a finite number of entry points for the tracer, each associated with an abstract subcompartment ofC. It is shown that the “hermaphroditic” property requires that the mean waiting time be infinite in at least one of the subcompartments, or in a subcompartment elsewhere in the system. A subcompartment with infinite mean waiting time must have some sort of memory, of infinite duration, which knows how long a given particle has been retained, however long that is, and thereby determines its probability of departure. Assuming, as seems likely, that no physical basis exists for such an infinite memory, it follows that “hermaphroditic” systems do not exist.
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    Bulletin of mathematical biology 42 (1980), S. 273-274 
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    Bulletin of mathematical biology 42 (1980), S. 275-275 
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    Bulletin of mathematical biology 42 (1980), S. 277-281 
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    Bulletin of mathematical biology 42 (1980), S. 267-272 
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    Notes: Abstract The implication of state space structure on the existence of a repeatable experimentE designed to determine if a states∈L has propertyP or notP is investigated. It is shown that if a state spaceL is connected, then no experimentE is repeatable. This formalism is used to demonstrate that if a propertyP has an associated set of points inL which is dense with dense complement inL, then there exists no repeatable experimentE which can be used to test whethers has propertyP or notP. Other consequences of this formalization are discussed.
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    Bulletin of mathematical biology 42 (1980), S. 282-282 
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    Bulletin of mathematical biology 42 (1980), S. 283-294 
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    Notes: Abstract It has been shown that the resistance of flow and the wall shear increase with the size of the stenosis but these increases are comparatively small due to non-Newtonian behaviour of the blood indicating the usefulness of its rheological character in the functioning of the diseased arterial circulation.
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    Bulletin of mathematical biology 42 (1980), S. 327-337 
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    Notes: Abstract The modern theory of generalized Hamiltonian systems is used to construct a unified canonical description of the linear Lagrangian biodynamics introduced by Kerner.
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    Bulletin of mathematical biology 42 (1980), S. 305-325 
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    Notes: Abstract The purpose of this paper is to justify an asymptotic method developed for the study of peristaltic transport in a tube of arbitrary cross section. Within the framework of long wave approximation, the three-dimensional nonlinear Navier-Stokes equations are reduced to a sequence of two-dimensional linear boundary value problems of Laplace and biharmonic operators. It is shown that, if a Reynolds number is less than some constant, the solution of the approximate equations is indeed an asymptotic approximation to the exact solution of the problem as the ratio of the maximum radius of the tube to the wave length of the peristaltic motion of the wall tends to zero, and the error estimates are expressed inL 2 norms. Furthermore, under the same condition the exact solution is shown to be unique and stable under arbitrary perturbation of spatially periodic disturbance. Application of the stability condition to peristaltic transport in a tube of circular cross section is given.
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    Bulletin of mathematical biology 42 (1980), S. 295-304 
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    Notes: Abstract A mathematical analysis, including existence and uniqueness, is given for some boundary value problems which model the flow of a fluid-solute mixture in a tube which is placed in an interstitium. The model permits an interchange of fluid and solute across the tube walls.
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    Bulletin of mathematical biology 42 (1980), S. 339-364 
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    Notes: Abstract The vertebrate nervous system has topographic interconnections in many parts, known for example as retinotopy, somatotopy, etc. It is plausible that modifiable synapses play an important role in forming and refining these connections together with the sensory experiences. To elucidate the mechanism of topographic organization, we propose a simple model consisting of two nerve fields connected by modifiable excitatory synapses. The model also includes modifiable inhibitory synapses. The behavior of the model is described by a set of simultaneous non-linear integro-differential equations. By analyzing the equations, we obtain the equilibrium solution of topographic connections. It is also proved that a part of the presynaptic field which is frequently stimulated comes to be mapped on a large area of the postsynaptic field so that it has a good resolution.
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    Bulletin of mathematical biology 42 (1980), S. 691-700 
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    Notes: Abstract The steady-state solution of the equations governing substrate exchange between vascular and extravascular compartments separated by a membrane with finite, symmetrical substrate permeability is presented. Substrate removal from the extravascular compartment by Michaelis-Menten saturation type kinetics with negligible diffusion in the axial and instantaneous diffusion in the transverse directions in both compartments are assumed. It is shown that the solution degenerates into known expressions for special linearized and asymptotic cases. The method of solution is also applied to an extension of the original model incorporating autoregulatory feedback effects upon the process responsible for substrate removal.
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    Bulletin of mathematical biology 42 (1980), S. 729-737 
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    Notes: Abstract Global asymptotic stability and equilibrium coexistence is established in two species Lotka-Volterra-type competition when there are time delays in interspecific interaction terms and the intraspecies competition is stronger than the interspecies competition.
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    Bulletin of mathematical biology 42 (1980), S. 739-746 
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    Notes: Abstract The realized (observed) value of Landau’s dominance hierarchy index is examined. Under a model of constant pairwise dominance probabilities, the observed index is shown to be a strongly consistent estimator of the underlying (true) index. However, a large number of encounters between animals is shown to be required in order to reduce bias and variance to practical levels except when the pairwise dominance probabilities are near one.
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    Bulletin of mathematical biology 42 (1980), S. 747-748 
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    Bulletin of mathematical biology 42 (1980), S. 749-749 
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    Bulletin of mathematical biology 42 (1980), S. 751-763 
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    Notes: Abstract The steady state potassium conductance as a function of measured membrane potential difference (p.d.) ϕ of the squid giant axon is corrected for the effect of accumulation of potassium in the periaxonal space. This correction is made on the assumption that several mathematical models of the axon are valid. These are (i) the McIlroy (1975), McIlroy-Hahn (1978) model of membrane conductanceg i(i=K, Na) which is a detailed model of passive transport of ions across the axonal membrane with the aid of mobile, negatively-charged carriers, (ii) the Adelmanet al. (1973) compartmental model of the periaxonal and external bathing-solution spaces, (iii) the enzymatic theory of nervous conduction due to McIlroy (1970 a, b, c), (iv) the Wien dissociative effect of the axolemmic electric field on the weak membrane buffer proposed by Bass and Moore (1968) as a trigger mechanism in nervous excitation and (v) the model (McIlroy, 1979) of the interfacial double-layer p.d.s. which are assumed to exist at the membrane’s surfaces because of the presence of a fixed surface charge. From the correctedg k (ϕ) curves the values of the double-layer p.d.s. of model (v) are deduced and these are shown to lead to a consistent, physically reasonable solution for the distance (approx. 6.8Å) between the fixed surface charges and for the dissociation constants of these sites in their interactions with the ions of the extra-membrane electrolytes. Assuming that the selectivity coefficint of the potassium conducting system for the squid giant axon is approx. 52 it is deduced that the potassium permeability,P ks , of the periaxonal barrier ≈1.37(±0.5)×10−4 cm sec−1 and the thickness of the periaxonal space ≈451±159Å.
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    Bulletin of mathematical biology 42 (1980), S. 797-805 
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    Notes: Abstract The effects of peripheral layer viscosity on physiological characteristics of blood flow through the artery with mild stenosis have been studied. It has been shown that the resistance to flow and the wall shear decrease as the peripheral layer viscosity decreases.
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    Bulletin of mathematical biology 42 (1980), S. 829-836 
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    Notes: Abstract A study was made of Higgins’ model of glycolysis incorporating molecular diffusion of intermediates, utilizing an earlier conjecture due to Landau. Conditions for the existence of asymptotically stable spatio-temporal periodic solutions are obtained.
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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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