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  • Springer  (69,649)
  • 1980-1984  (44,784)
  • 1965-1969  (24,865)
  • 1960-1964
  • 1925-1929
  • 1983  (44,784)
  • 1965  (24,865)
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  • 1980-1984  (44,784)
  • 1965-1969  (24,865)
  • 1960-1964
  • 1925-1929
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  • 1
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    Bulletin of mathematical biology 45 (1983), S. 287-293 
    ISSN: 1522-9602
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract We postulate that the biomass distribution function for an ecological population may be derived from the condition that the biomas diversity functional is maximal subject to an energetic constraint on the total biomass. This leads to a biomass distribution of the form $$p(m) = \bar m^{ - 1} \exp ( - m/\bar m)$$ , where $$\bar m$$ is the mean biomass per individual. The same condition yields a unique value for the biomass diversity functional. These predictions are tested against fishery data and found to be in good agreement. It is argued that the existence of a unique value for biomass diversity may provide a preliminary theoretical foundation for the observed upper limit to species diversity.
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    Bulletin of mathematical biology 45 (1983), S. 311-321 
    ISSN: 1522-9602
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    Notes: Abstract Pigment distribution presages hydranth regeneration in the marine hydroidTubularia. We suggest that such a distribution could result from a reaction-diffusion system. A model system based on a practical reaction scheme is studied and spatial structures found which closely resemble this pigment distribution. Finite-amplitude spatial structures in reaction-diffusion systems are considered. Whereas in one spatial dimension the final structures are normally very similar to the transient patterns which emerge from a linear analysis, it is shown that in more than one dimension this is not necessarily the case. The reasons for this are discussed.
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    Bulletin of mathematical biology 45 (1983), S. 409-424 
    ISSN: 1522-9602
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    Notes: Abstract An analytical model is used to described the behavior of inhaled particulate matter in the human respiratory tract. Three different geometries, symmetric and asymmetric, are utilized to simultate the tracheobronchial (TB) tree. The suitability of each geometry for representing the human is evaluated by comparing calculated aerosol deposition probabilities with experimental data from inhalation exposure tests. A symmetric, dichotomously branching pattern is found to be a reliable description of the TB tree for studies of factors affecting aerosol deposition in the human lung. Calculations with the theoretical model are in excellent agreement with measured aerosol deposition efficiencies. Furthermore, the model accurately predicts experimentally observed features of inhalation exposure data, such as effects of inter-subject lung morphology differences and relative efficiencies of specific deposition mechanisms, on aerosol deposition patterns in the TB tree.
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    Bulletin of mathematical biology 45 (1983), S. 436-436 
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    Bulletin of mathematical biology 45 (1983), S. 437-437 
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    Bulletin of mathematical biology 45 (1983), S. 579-590 
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    Notes: Abstract In this paper we are concerned with problems of the long-term behavior for nonlinear systems in random environment. The general model is assumed to be given by an ordinary differential equation with random parameters or random input. The disturbance process can be taken from a fairly general class of Markov processes having a bounded state space. In terms of the system’s dynamics we give sufficient conditions for the existence and uniqueness of invariant probabilities. Finally, we apply these results to the two-dimensional biochemical model which is known as the Brusselator.
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    Bulletin of mathematical biology 45 (1983), S. 571-577 
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    Notes: Abstract In various applications one faces the problem of estimating a signal from discontinuous observations. For example, in biomedical applications the signal may be the ‘state’ of a given organ and one observes through an external counter the amount of radioactivity sequestered by the organ after injection of a radioactive tracer. Here the problem is studied in the context of nonlinear filtering when the signal can be modelled as either a random variable or a diffusion process, and the observations have a continuous and a purely discontinuous component; both components may be affected by the signal. When the signal is a random variable an explicitly computable solution is obtained; for the diffusion case the solution is given as a sequence of approximating filters that can be computed recursively.
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    Bulletin of mathematical biology 45 (1983), S. 627-634 
    ISSN: 1522-9602
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    Notes: Abstract Eigenvalue problems arise in various biological models. We outline a useful comparison method and a technique using Lyapunov functions that can be applied in many cases. An application to lateral diffusion is discussed.
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    Bulletin of mathematical biology 45 (1983), S. 605-616 
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    Notes: Abstract This paper reviews, up to their recent developments, two types of models of the cell cycle: those considering the size controls over the cycle events and the transition probability models. The distribution of inter-mitotic time and the sister-sister and motherdaughter correlations implied by the two approaches are discussed in view of some relevant experimental data.
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    Bulletin of mathematical biology 45 (1983), S. 617-626 
    ISSN: 1522-9602
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    Notes: Abstract The development of a blood cell line originating from a pluripotent stem cell pool is modelled by a chain of multidimensional branching processes in which the sojourn times of the cells in certain resting states depend on the size of the following subpopulation. The stability of such a model is discussed qualitatively and some considerations concerning a possible malignant degeneration are presented. The behaviour of models for normal and malignant cell production are illustrated by stochastic stimulations. The model presented here describes the development of a certain line of blood cells (e.g. erythrocytes, monocytes or granulocytes) originating from the pluripotent stem cell up to the functional cell in the blood (for related models see, e.g., Rubinow and Lebowitz,J. math. Biol. 1, 87–225;Biophys. J. 16, 897–910).
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    Bulletin of mathematical biology 45 (1983), S. 635-641 
    ISSN: 1522-9602
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    Notes: Abstract This paper reviews some recent advances in single population stochastic differential equation growth models. They are a natural way to model population growth in a randomly varying environment. The question of which calculus, Itô or Stratonovich, is preferable is addressed. The two calculi coincide when the noise term is linear, if we take into account the differences in the interpretation of the parameters. This clarifies, among other things, the controversy on the theory of niche limiting similarity proposed by May and MacArthur. The effects of correlations in the environmental fluctuations and statistical methods for estimating parameters and for prediction based on a single population trajectory are mentioned. Applications to fisheries, wildlife management and particularly to environmental impact assessment are now becoming possible and are proposed in this paper.
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    Bulletin of mathematical biology 45 (1983), S. 643-658 
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    Notes: Abstract A survey is given of the application of (functions of) continuous-time Markov chains in the statistical analysis of behavioural time series.
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    Bulletin of mathematical biology 45 (1983), S. 659-659 
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    Bulletin of mathematical biology 45 (1983), S. 661-664 
    ISSN: 1522-9602
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    Notes: Abstract This paper demonstrates that there is one and only one solution to a non-linear singular two-point boundary-value problem which describes oxygen diffusion in a spherical cell. Previous authors have calculated numerical results that differ substantially. Numerical computations using the multiple shooting method support the results of McElwain.
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    Bulletin of mathematical biology 45 (1983), S. 665-720 
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    Notes: Abstract The mathematics of distance geometry constitutes the basis of a group of algorithms for revealing the structural consequences of diverse forms of information about a macromolecule's conformation. These algorithms are of proven utility in the analysis of experimental conformational data. This paper presents the basic theorems of distance geometry in Euclidean space and gives formal proofs of the correctness and, where possible, of the complexity of these algorithms. The implications of distance geometry for the energy minimization of macromolecules are also discussed.
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    Bulletin of mathematical biology 45 (1983), S. 721-737 
    ISSN: 1522-9602
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    Notes: Abstract A fully developed pulsatile flow in a circular rigid tube is analysed by a microcontinuum approach. Solutions for radial variation of axial velocity and cell rotational velocity across the tube are obtained using the momentum integral method. Simplified forms of the solutions are presented for the relevant physiological data. Marked deviations in the results are observed when compared to a Newtonian fluid model. It is interesting to see that there is sufficient reduction in the mass flow rate, phase lag and friction due to the micropolar character of the fluid.
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    Bulletin of mathematical biology 45 (1983), S. 749-758 
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    Notes: Abstract A mathematical model of the transport of fluorescein across the blood-retina barrier in the transient state and the subsequent diffusion of fluorescein in the vitreous body is presented. The function of the barrier is lumped in a single parameter—the permeability. The sensitivity of this parameter due to changes in the other parameters of the model is given. This establishes the foundation for the quantitative assessment of the barrier function through vitreous fluorophotometry.
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    Bulletin of mathematical biology 45 (1983), S. 739-748 
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    Notes: Abstract The objective of this preliminary study was to develop a new quantitative method of setting the initial insulin infusion patterns in treatment of diabetic patients. The method is based upon the mathematical estimation of the insulin profile required to maintain the glucose level within the normal range after glucose loading in diabetic patients. Using our previously developed equivalent circuit model of glucose kinetics and the reported data of an intravenous glucose tolerance test (IVGTT) in two groups of normal and diabetic patients, two important physiological parameters of the model (the peripheral tissue's insulin resistivity and the hepatic sensitivity to glucose level) were computed for two clinical groups. Then the insulin profile was obtained by computing the plasma insulin concentrations required to keep the total glucose utilization rate of the tissue and the liver in the diabetic group equal to that of the normal group. The simulation result indicated that the computed insulin profile produced a plasma glucose profile which was more closely matched to the normal group's glucose profile than with the case of emulating the normal group's insulin profile in the diabetic group.
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    Bulletin of mathematical biology 45 (1983), S. 759-780 
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    Notes: Abstract This paper shows that the Na conductance changes can be explained quantitatively, based on the following assumptions: (1) there exist in nerve membranes the electron transfer (ET) complexes and traps, (2) there is energy migration among them. The gating mechanism is explained in physical terms. Its mathematical expression differs from the Hodgkin-Huxley equations, but resembles the Hoyt formulation. In the present model, the physical parameters for the squid axon can be estimated from currently available experimental data. The density of the ET complexes is on the order of 105/μm2, and the density of the traps is 103/μm2. The magnitude of the energy transfer rate between ET complexes is about 106/sec at large depolarization and decreases with decreasing depolarizations, as does the Na inactivation rate. The energy gap between the two stable states of the transfer electron in the ET complex is estimated to be around 0.1 eV, which is approximately the same as that for the photosynthetic systems.
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    Bulletin of mathematical biology 45 (1983), S. 781-792 
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    Notes: Abstract The role of symmetry in simplifying the theory of complex neural systems is argued. When the structural symmetries of a network are expressed as an ismorphism group, implications emerge for the dynamics. Various qualitative possibilities concerning stability of uniform motion in homogeneous nets are discussed and an approach to neural hierarchies is outlined.
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    Bulletin of mathematical biology 45 (1983), S. 793-805 
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    Notes: Abstract By constructing appropriate Liapunov functionals, asymptotic behaviour of the solutions of various delay differential systems describing prey-predator, competition and symbiosis models has been studied. It has been shown that equilibrium states of these models are globally stable, provided certain conditions in terms of instantaneous and delay interaction coefficients are satisfied.
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    Bulletin of mathematical biology 45 (1983), S. 807-826 
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    Notes: Abstract Sensitivity analyses have been used to examine the flow structure of two hypothetical ecosystem models. These analyses have results which relate to important aspects of ecosystem theory. Cycles are shown to increase the sensitivity of the network, while increased throughflow is shown to decrease the sensitivity. Such results indicate that several factors can be modified to decrease the sensitivity of ecosystems to environmental stress.
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    Bulletin of mathematical biology 45 (1983), S. 827-836 
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    Notes: Abstract A continous, deterministic mathematical model is used to predict population distributions by age at any time, given the initial distribution and the variation of birth and death rates with age and time. Solutions are obtained on a computer using a semi-discretization algorithm in which time derivatives in the partial differential equations are replaced by finite-difference expressions. The resulting sets of ordinary differential equations are solved by a predictor-corrector method. Graphical results are shown for some examples.
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    Bulletin of mathematical biology 45 (1983), S. 849-855 
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    Notes: Abstract A new formula for the complexity of graphs is proposed and applied to the points lines and ‘connections’ of some chemically relevant graphs.
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    Bulletin of mathematical biology 45 (1983), S. 837-847 
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    Notes: Abstract This paper reports general and specialized results on analytical solutions to the governing phenomenological equations for chemotactic redistribution and population growth of motile bacteria. It is shown that the number of bacteria cells per unit volume,b, is proportional to a certain prescribed function ofs, the concentration of the critical substrate chemotactic agent, for steady-state solutions through an arbitrary spatial region with a boundary that is impermeable to bacteria cell transport. Moreover, it is demonstrated that the steady-state solution forb ands is unique for a prescribed total number of bacteria cells in the spatial region and a generic Robin boundary condition ons. The latter solution can be approximated to desired accuracy in terms of the Poisson-Green's function associated with the spatial region. Also, as shown by example, closed-form exact steady-state solutions are obtainable for certain consumption rate functions and geometrically symmetric spatial regions. A solutional procedure is formulated for the initialvalue problem in cases for which significant population growth is present and bacteria cell redistribution due to motility and chemotactic flow proceeds slowly relative to the diffusion of the chemoattractant substrate. Finally, a remarkably simple exact analytical solution is reported for a stradily propagating plane-wave which features motility, chemotactic motion and bacteria population growth regulated by substrate diffusion.
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    Bulletin of mathematical biology 45 (1983), S. 857-867 
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    Notes: Abstract This paper discusses the flow of blood in large artries under the influence of linear periodic acceleration. The governing equations and boundary conditions are established and analytical solutions for the velocity, fluid acceleration, bulk flow and shear stress are obtained. The results for these physical quantitites are computed for the case of an artery the size of a normal human aorta. It is found that the flow field variables are directly proportional to the external accelerating force. The behaviour of the velocity profile along the radial distance at different stages of times at fixed applied acceleration is also shown.
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    Bulletin of mathematical biology 45 (1983), S. 931-968 
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    Notes: Abstract The evolutionary selection circuits model of learning has been specified algorithmically. The basic structural components of the selection circuits model are enzymatic neurons, that is, neurons whose firing behavior is controlled by membrane-bound macromolecules called excitases. Learning involves changes in the excitase contents of neurons through a process of variation and selection. In this paper we report on the behavior of a basic version of the learning algorithm which has been developed through extensive interactive experiments with the model. This algorithm is effective in that it enables single neurons or networks of neurons to learn simple pattern classification tasks in a number of time steps which appears experimentally to be a linear function of problem size, as measured by the number of patterns of presynaptic input. The experimental behavior of the algorithm establishes that evolutionary mechanisms of learning are competent to serve as major mechanisms of neuronal adaptation. As an example, we show how the evolutionary learning algorithm can contribute to adaptive motor control processes in which the learning system develops the ability to reach a target in the presence of randomly imposed disturbances.
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    Bulletin of mathematical biology 45 (1983), S. 981-990 
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    Notes: Abstract In the present paper we discuss the behaviour of solutions of a dynamical system describing the growth of cells in a well-mixed continuous culture where the supply of the growth-limiting nutrient depends on the activity of an enzyme outside the cell membrane. It turns out that for positive dilution rates there exists an exponentially attractive two-dimensional simplex. Furthermore, the reversed system restricted to this simplex is quasimonotone. In every case all trajectories tend to an equilibrium state.
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    Bulletin of mathematical biology 45 (1983), S. 991-1004 
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    Notes: Abstract We present a Gause predator-prey model incorporating mutual interference among predators, a density-dependent predator death rate and a time lag due to gestation. It is well known that mutual interference is stabilizing, whereas time delays are destabilizing. We show that in combining the two, a long time-lag usually, but not always, destabilizes the system. We also show that increasing delays can cause a bifurcation into periodic solutions.
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    Bulletin of mathematical biology 45 (1983), S. 969-980 
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    Notes: Abstract The cycle structure of enzymatic neural networks may be characterized in terms of number of cycles exhibited, size of cycle state sets and cycle lengths. Simulation experiments show that the stability properties of these networks have some unusual features which are not exhibited by networks of two-state switching elements or by randomly constructed ecosystem models. The behavioral and structural stability of these systems decreases with their structural complexity, as measured by the number of components. The behavioral and structural stability of enzymatic neural networks also decreases with structural complexity, as measured by the number of excitase types, but only up to the middle level of excitases per neuron. This is the point of highest potential responsiveness of the system to environmental stimuli. Beyond this point the behavioral and structural stability increase. This is due to the fact that the number of possible states increases up to this point and decreases beyond it. The number of possible states, not the number of components, serves as the useful measure of complexity in these types of systems. The selection circuits learning algorithm has been used to evolve networks whose cycle structures have desired features.
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    Bulletin of mathematical biology 45 (1983), S. 1005-1011 
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    Notes: Abstract Similarity criteria of the functional design of the mammalian cardiovascular system are scant. For the analysis of mammalian cardiac energetics physiological parameters such as mean arterial blood pressure, stroke volume, heart rate, metabolic rate and heart and body weights are considered pertinent. Based on these parameters, a new similarity principle is established via allometric equations, dimensional analysis and Buckingham's pi-theorem. The principle states that the ratio of left ventricular external work to metabolic rate is inversely proportional to resting heart rates of mammals. The proportionality constant is dimensionless and is invariant of mammalian body weights.
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    Bulletin of mathematical biology 45 (1983), S. 1029-1045 
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    Notes: Abstract The mathematical theory of categories is used as a tool in the description of the structure and function of natural systems. The connections between the category of natural systems, with observables and dynamics, and the phenomenological calculus of response tensors, duality- and adjoint-invariance diagrams are established. The unified theory is applied to the analysis of hierarchies, pattern generation and the structure and dynamics of proteins.
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    Bulletin of mathematical biology 45 (1983), S. 1047-1072 
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    Notes: Abstract This is an investigation of natural systems from the standpoint of the mathematical theory of categories. It examines the relationships which exist between different descriptions through measurement of observables and dynamical interactions. We begin with a category theory of formal systems with observables, and then proceed to a category theory of dynamical systems. The two categories are then combined to represent natural systems. Topological considerations enter in the study of stability and bifurcation phenomena. Special emphasis is placed on natural systems which model biological processes. The categorical system theory developed is applied to the analysis of several biological problems and biological system theories.
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    Notes: Abstract Tetanic hyperpolarization for theXenopus node is simulated by means of iterative solutions of the Frankenhaeuser-Huxley excitation equations together with an active transport current density term which is dependent on sodium and potassium levels as well as the ADP/ATP ratio. All time-dependent variables at the end of one interspike interval are introduced as initial conditions for the next response, whereupon all time-dependent changes in voltage and permeability factors appear identical for the third and fourth responses of a sequence. Net change in internal sodium concentration is zero throughout the third and fourth intervals if sodium loading of the system is initially adjusted to a critical level. Extent of tetanic hyperpolarization is a function of the pump conductance.
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    Bulletin of mathematical biology 45 (1983), S. 1097-1097 
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    Bulletin of mathematical biology 45 (1983), S. 1073-1096 
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    Notes: Abstract The properties of nonlinear equations describing the solute and solvent transport across a simplified Patlak-Goldstein-Hoffman model (two membranes in series without unstirred layers) are investigated both analytically and numerically. The analysis shows that the principal coefficients measured in transport experiments in the presence of active transport are dependent on the experimental conditions. These ‘apparent’ system parameters are extensions of the corresponding parameters determined both in passive systems and in the linear Kedem-Katchalsky theory. Moreover, they are related to the local phenomenological coefficients of the single membranes of the array. Several relationships between measurable quantities and the local system parameters are indicated, allowing the planning of experiments aimed at the measurement of the latter. Data in the literature have been used to check the proposed volume flow equation.
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    Bulletin of mathematical biology 27 (1965), S. 49-63 
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    Notes: Abstract Compartmental systems can be represented by direct graphs in which each node corresponds to a generating function and each arm to a transfer generating function. A homomorphism is established between a compartmental system and this representation, in analogy with that obtained through the use of the Laplace transformation. From the values obtained experimentally in a given compartment, through the solution of a difference equation, the generating function for the corresponding node can be calculated and the graph of the system can be built up within the degrees of freedom of the model. From the graph it is possible to calculate the transfer generating function between any two connected nodes, the mean permanence time in a given node, the mean transit time between two nodes, and their precursor-successor order.
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    Bulletin of mathematical biology 27 (1965), S. 85-89 
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    Notes: Abstract The Competitive Exclusion Principle, formulated by V. Volterra (Memorie del R. Comitato Talassografico Italiano,131, 1–142, 1927) for a number of species competing for a common ecological niche, is extended to a number of species competing for many ecological niches.
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    Bulletin of mathematical biology 27 (1965), S. 65-70 
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    Notes: Abstract A modification is presented of an earlier theory of the mixing of dye following injection into the circulation. Approximate theoretical relations are given for the concentration of dye in the right heart and in the aorta following right atrial injection. It is shown that when the probability distribution of transit times around the circulation has a prolonged tail, mixing waves are now inscribed about a quasi-exponential relation. Later in time the relation levels off to a uniform asymptotic concentration corresponding to an equilibrium volume of dilution.
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    Bulletin of mathematical biology 27 (1965), S. 91-104 
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    Notes: Abstract The adsorption of two cations at the anionic sites of a polymer (e.g., such as a protein) in an electric fields is discussed, taking into account cooperative interaction of the cations mediated through the backbone of the polymer. The calculation of the grand partition function explicitly considers the vacant negative sites of the polymer. As in the case without cooperative interaction, the problem reduces to the determination of the largest eigenvalue of asymmetric matrices. The weights of the different neighbor configurations are determined. Approximate formulae for the grand partition function and for those weights are derived. The formal analogy of these cooperative phenomena and those occurring in quantum (bio)chemistry is pointed out exemplifying an earlier suggestion about the basis of quantum biology.
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    Bulletin of mathematical biology 27 (1965), S. 105-112 
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    Notes: Abstract The transformation from gel to sol in cell cytoplasm is treated as the transition from a lattice of macromolecules linked by Ca++ ions to a random distribution of the macromolecules. The transition is a cooperative process, whose probability is expressed in terms of the theory of runs. The process is related to cell metabolism by the assumption that available Ca++ concentration is regulated by metabolically produced endogenous chelating agents.
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    Bulletin of mathematical biology 27 (1965), S. 113-118 
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    Notes: Abstract Kinetic criteria for solid state physical mechanisms of electron and ion transport in biological systems are summarized, and the mechanisms are discussed. A reaction which is rate-limited by electron or ion transport across a particle or membrane in accord with Ohm's law will show first order kinetics, with an hyperbolic relationship between rate constant and the sum of substrate plus product. Larger initial substrate concentrations produce smaller rate constants, thus giving the appearance of substrate inhibition. Examples are cytochrome oxidase and peroxidase, and pyruvate carboxylase. Ohmic transport mechanisms may be caused by electron conduction or superconduction through protein, by electron conduction through water, or by conduction of ions through membranes. A reaction which is rate-limited by charge transport across an activation energy barrier at an interface in accord with a logarithmic voltage-current law will show reaction kinetics conforming to the Elovich equation, and will have the appearance of a pair of simultaneous first order processes. Examples include decay of photogenerated free radicals in eye melanin particles and in photosynthetic particles of bacteria, and sodium and potassium ion transport across cell surfaces. The logarithmic voltage-current law may be regarded as an empirical relationship describing behavior of interfaces, justified by extensive experimental data on many types of interfaces, or it may be derived theoretically for individual cases from statistical mechanical and/or solid state physical considerations.
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    Bulletin of mathematical biology 27 (1965), S. 119-130 
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    Notes: Abstract When aortic pressure curves were predicted previously on the basis of a newly developed model of visco-elastic properties of the aorta, it was necessary to use published viscoelastic constants. These were usually obtained from longitudinal strips of blood vessels long removed from the animal, and therefore probably containing deteriorated smooth muscle. The predicted curves had the same form as actual tracings, substantiating the analysis somewhat, but the pressure levels were low. These low levels, if due to inadequate visco-elastic constants, could be attributed to the use of longitudinal rather than circumferential segments as well as to the use of segments with deteriorated muscle. The present analysis uses data collected by the author testing circumferential viscoelastic properties of fourteen different aortic regions in a way suggested by the author's model of an aortic wall. Moreover, the constants were measured on segments containing muscle relaxed by EDTA solutions and on similar segments containing muscle contracted by neosynephrine. These visco-elastic constants were used in the author's nonlinear differential equation of motion of the aortic wallin vivo to predictin vivo pressure curves. The predicted curves were low in any given aortic region if relaxed constants were used, but at normal levels with contracted constants. In fact, pressure curves predicted using constants obtained from aortic segments containing contracted muscle resembled actual tracings in form and pressure levels. Even the observed variations in the form of the systolic pressure curve down the aorta were predicted by this analysis.
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    Bulletin of mathematical biology 27 (1965), S. 131-133 
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    Notes: Abstract It is an empirical finding that an allometric quantity with dimensional exponents α, β and γ relative to mass, length, and time, respectively, has a value for its allometric exponentb satisfying the relation $$\tfrac{1}{3}(3\alpha + \beta + {\gamma \mathord{\left/ {\vphantom {\gamma 2}} \right. \kern-\nulldelimiterspace} 2}) \leqslant b \leqslant \tfrac{1}{3}(3\alpha + \beta + \gamma ).$$ A theoretical derivation is given of this double inequality using only the fact of constant density and the plausible assumption that metabolic rate is a dominant allometric quantity.
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    Bulletin of mathematical biology 27 (1965), S. 135-143 
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    Notes: Abstract C. Shannon's definition (Bell System Technical Journal,27, 379–423, 1948) of the entropy of a continuous distribution is dimensionally incorrect and does not have the same significance as the corresponding definition in the discrete case. A new definition is proposed: this modified entropy is more like the entropy of a discrete distribution in one way, in another more like Shannon's “transmission rate.” The ideas are illustrated by reference to Wright's study of the hereditary influence on the coat pattern of the guinea pig.
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    Bulletin of mathematical biology 27 (1965), S. 145-150 
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    Notes: Abstract In the following paper, a possible mode of evolution is described which differs from the traditional modes in not being selective in the Darwinian sense.
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    Bulletin of mathematical biology 27 (1965), S. 177-181 
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    Notes: Abstract A description of the kinds of systems susceptible to information theoretical analysis is given. By means of an example, certain common fallacies in the application of communication theory to biology are illustrated. The entropy-information analogy is discussed. *** DIRECT SUPPORT *** A01E2109 00008
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    Bulletin of mathematical biology 27 (1965), S. 161-175 
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    Notes: Abstract A mathematical model of a process contains parameters supposedly characterizing the system which manifests the process. If the parameters are statistically distributed in a population of such systems, the process manifested by the entire population will in general be described by a different mathematical model. Thus a choice is always at hand between two or more mathematical models, depending on which parameters (if any) are assumed to be distributed and, if so, how. Examples of such alternative interpretations are given for mathematical models of some behavioral processes.
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    Bulletin of mathematical biology 27 (1965), S. 191-202 
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    Notes: Abstract The problem of economically linking a large number of stimuli with a large number of potential responses is considered to resemble a problem of efficient retrieval of documents (the responses) on the basis of their characterization by descriptors (the stimuli to which the responses are appropriate). In this retrieval problem, a method whereby the codes for descriptors are random positions in a coding field, and whereby codes for all applicable descriptors are superimposed in the same field, seems to be the simplest way of avoiding serious difficulties of retrieval. After a review of this method, the possibility is considered that very simple neural mechanisms could embody the essential features of the method. The aim of the discussion is to learn whether very simple structures and patterns of reinforcement would be adequate to carry out useful information processing in the brain, and to show some conceivable functions of simple neural networks which the experimenter might keep in mind. The discussion also shows how the structure of a simple “perceptron”-like network is suggested by the requirements of a retrieval task.
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    Bulletin of mathematical biology 27 (1965), S. 223-233 
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    Notes: Abstract A model is proposed to relate the regeneration of the ERGa-wave after partial light adaptation to the level of the light adaptation. The model assumes that thea-wave amplitude is a function of some reactive substance associated with ana-wave generator. The maximuma-wave amplitude occurs when the eye is fully dark adapted, and thea-wave generator initiator concentration is at a maximum. Thea-wave generator initiator concentration can be decreased by interacting with a product of the rhodopsin-light energy reaction, and increased by removal of this inhibitor. The removal of the inhibitor depends upon the isomerization of the all-trans-retinene to the 11-cis form. An excess of inhibitory material overa-wave generator initiator would cause a delay in the appearance of thea-wave until the excess inhibitory material is removed. This delay is a linear function of the logarithm of the adapting energy. The agreement of this model with the experimental ERG data is very good.
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    Bulletin of mathematical biology 27 (1965), S. 215-222 
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    Notes: Abstract The survival rate of fishes in their earlier stages of development and the influencing factors present one of the most fundamental problems of fish population dynamics. After I. Hjort's (Cons. L.'explor. Ner.,20, 3–228, 1914) work, there have been many investigators in this field and there is no doubt about the very important role of ova and larvae mortality in the fate of a given fish generation. Less clear are the ideas concerning factors determining the high mortality of fishes in their earlier stages of development; especially the factor of food supply of larvae during the period of transition to exogenic nutrition. The value of this factor has been estimated differently from different points of view. For example, R. J. H. Beverton and S. J. Holt (On the Dynamics of Exploited Fish Population, 1957) have given to the food supply factor its deserved importance. On the other hand, T. V. Dekhnik (Trudy Sevastopolskoi Biologicheskoi Stantsii,13, 216–244, 1960;Ibid.,14, 222–243, 1961) has proved in her investigations that at least for pelagic larvae of Black Sea fishes there is an excessive amount of food, and that therefore food cannot play an important role in larva survival. Not wanting to stop to review the literature of the problem (see Dekhnik,Trudy Sevastopolskoi Biologicheskoi Stantsii,13, 216–244, 1960), we will only remark that the problem as a whole needs further investigation. Not only new data are needed, but also methods for following up analysis have to be worked out.
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    Bulletin of mathematical biology 27 (1965), S. 253-259 
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    Notes: Abstract The investigation described here is anexperimental one which brings to light some new facts and confirms others already reported. They partly concern the hysteresis phenomena handled by N. Rashevsky (Mathematical Biophysics, 1960) and partly provide a point of departure for future biophysical research to be undertaken by biomathematicians.
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    Bulletin of mathematical biology 27 (1965), S. 27-52 
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    Notes: Abstract The aortic pressure curve necessarily reveals the mechanical properties of the aorta and peripheral resistance as well as of the dynamics of blood flow. The present study uses a reasonable model of visco-elastic properties of the aorta, a reasonable form for variations in peripheral resistance and blood flow to predict an aortic pressure tracing. Numerical values of constants measured experimentally were available in the published literature. These were used in the nonlinear differential equations of motion of the system under analysis. The equations yielded to piece-wise solution, giving the aortic circumference and the aortic pressure as functions of time. The form of both curves resembles clinical tracings, but numerical values of circumference were higher and of pressure lower thanin vivo. The discrepancies between predicted and clinical curves may reveal certain inadequacies in published measurements on visco-elastic constants. These measurements have been made on longitudinal rather than circumferential strips often containing dead rather than living muscle. The discrepancies, therefore, indicate specific gaps in our knowledge of aortic behaviorin vitro. The suggested model of the system aided in the design of experiments which could supply data necessary to substantiate or to revise the model.
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    Bulletin of mathematical biology 27 (1965), S. 373-377 
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    Notes: Abstract Some aspects of the circulation through the veins remain unexplained. The pressure gradient which ordinarily exists across a large vein, for example, is much greater than that necessary to maintain the same flow through a rigid tube of identical diameter (Brecher, 1956; Starling and Evans, 1962). During inspiration, blood flow through the thoracic portion of the inferior vena cava increases markedly, while that through the distal abdominal portion does not change. Furthermore, an active source of pressure drop in the chest is necessary to maintain venous flow. For the open chest the pressure drop occurs mainly during ventricular contraction, while in the closed chest it is produced chiefly by inspiration. The present study indicates that the high distensibility of the veins accounts in significant degree for the behavior characteristic of the venous circulation.
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    Bulletin of mathematical biology 27 (1965), S. 379-387 
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    Notes: Abstract This paper is an attempt to provide a logical model for the process of growth and differentiation in a multi-cellular organism. More specifically it is intended to show how genetic information relating to macroscopic structure and coded in the form of a logical tree could be progressively embodied in the organism as it develops by repeated division from a single cell. The aim is to establish biological analogies rather than mathematical interest, and reproduction, adaption, and the coordinating action of hormones are discussed within the general logical framework.
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    Bulletin of mathematical biology 27 (1965), S. 407-415 
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    Notes: Abstract Models having the form of surfaces of revolution may be used to represent the urethra under pre-voiding pressure. From such models are derived formulas for calculating muscle tension from the shape of a urethragram.
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    Bulletin of mathematical biology 27 (1965), S. 389-406 
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    Notes: Abstract The calculation of rates of entry of material into an open system of multiple pools in the steady state from the specific activities of end products, which may be derived from several pools, is described. This analysis may be applied to estimate the rates of secretion of steroid hormones from the specific activities of urinary metabolites which may have various hormones as common precursors. In a previous publication (Gurpideet al., 1963) formulae have been presented by which secretory rates could be calculated after a single injection of the tracers assuming that each of the urinary metabolites was uniquely derived from one of the pools in the system. In the present article similar formulae were derived without this assumption. Consequently, it is shown that, under certain circumstances, non-uniquely derived metabolites can be used to estimate secretory rates, and that it may be unnecessary to consider the pathways of conversion of the hormones to the metabolites or the sites where these conversion occur.
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    Bulletin of mathematical biology 27 (1965), S. 431-434 
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    Notes: Abstract The sensitivity and “specificity” of measurements for the determination of transferates are enhanced by the use of an additional radiotracer, serving to trace the unlabelled substance. This method presents advantages mostly in systems outside their steady state but only exeptionally in steady state systems.
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    Bulletin of mathematical biology 27 (1965), S. 417-429 
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    Notes: Abstract An integral equation approach to perturbation-tracer analysis in steady-state multicompartment systems is formulated. The theory is developed for δ function perturbation and tracer inputs and extended to the case of continuous small perturbations and continuous tracer inputs. It is shown that the first order dependence of the initial entry function can then be expressed by means of an integral equation: $$B_1 (t) = \int_{t_2 = - \infty }^\infty {\int_{t_1 = - \infty }^\infty {P(t_1 )T(t_2 )B_1 (t - t_2 ,t_1 - t_2 )dt_1 dt_2 } } $$ whereB 1(t) is the first order initial entry function for the tracer material,P(t1) the perturbation function.T(t 2) is the tracer input function, andB 1(t−t 2 ,t 1 −t 2 ) is a continuous function of two variables characterizing the first order perturbation-tracer response of the system.
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    Bulletin of mathematical biology 27 (1965), S. 435-447 
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    Notes: Abstract A correspondence is established between a tangible model of brain structure (and function) and a system of observer-observed interactions. The observed quantities are “stimuli” in the form of signal amplitude distributions in a mass of neuron-like units; the observer is a set of neurons (not circumscribed in a local region) in which a distributed parameter mirrors the stimulus history of the set, i.e., represents a “memory”. Utilizing the theory of the Perceptron, a contemporary brain model, it is demonstrated that large systems composed of many observer-observed interactions exhibit quantum mechanical behavior on a “macroscopic” scale. This behavior entails wave-like phenomena and the need of applying the superposition mechanics to system information content calculations.
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    Bulletin of mathematical biology 27 (1965), S. 449-471 
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    Notes: Abstract This is the continuation of Part I, which was published in the September, 1965, issue of theBulletin. The birth rate, α(t), is now assumed to be a linear functional of the age density,n. This gives a simple model of self-replenishing stem cell compartments, and leads to a necessary condition for the existence of a steady state. Some examples are presented to illustrate the formalism. They include: (a) An equivivant population with life spanD and no losses from death or migration. The total number of cells is multiplied by 2 in each time intervalD. As a special case, frequently realized in practice, the population may be increasing exponentially with time (“log-phase” of growth). (b) A compartment with “random” emigration of cells and gamma distribution of life spans. (c) An oversimplified version of L. G. Lajtha’s model describing stem cell kinetics. In section IV a simple case in which the loss function depends explicitly onn is discussed very briefly.
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    Bulletin of mathematical biology 27 (1965), S. 473-476 
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    Notes: Summary Mathematical models of nonuniform gas distribution in the lungs which assume a two-chambered lung to be ventilated through a third chamber, i.e. a common dead space, have led to diverging results. A breath-by-breath analysis of such a system results in a two-exponential solution whereas a continuous ventilation analysis gives a three-exponential solution. This is caused by the different assumptions made in the two models about the composition of dead space gas. In the breath-by-breath analysis one assumes that theN 2 content of the dead space is zero at the end of inspiration. In the continuous ventilation model one assumes that theN 2 content in the dead space is unknown at all instants during the breathing cycle. No physical significance should be attached to any chamber in this type of analysis. The continuous ventilation model provides a more general solution than the cyclical ventilation model, because the former treats the common dead spaces as an independent unknown.
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    Bulletin of mathematical biology 27 (1965), S. 493-495 
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    Bulletin of mathematical biology 27 (1965), S. 477-491 
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    Notes: Abstract The different approaches to relational biology developed by N. Rashevsky and R. Rosen consider essentially binary relations between various components of biological functions of the organism. Actually an organism is represented by a set of differentn-ary relations. The present paper is an attempt to outline a possible approach to this more realistic situation. Inasmuch asn-ary relation is ann-place predicate, it is attempted to describe the basic known properties of an organism in terms ofn-place predicates, in which the variables represent the different “components” of the organism. Some possible forms of such predicates are discussed and some general properties of systems of such predicates are studied. It is shown that if the organism is described by predicates of the type discussed here, statements can be derived about the conditions “of reestablishability” of different components. Conclusions similar to those obtained previously by R. Rosen are reached now on a very different basis. A description of the process of cell differentiation in multicellular organisms in terms of predicates studied here is briefly outlined. A comparison of similarities and differences between the approach and Rosen’s description of organisms in terms of the theory of categories is made.
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    Bulletin of mathematical biology 27 (1965), S. 497-500 
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    Bulletin of mathematical biology 27 (1965), S. 503-503 
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    Bulletin of mathematical biology 27 (1965), S. 501-502 
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    Bulletin of mathematical biology 45 (1983), S. 139-142 
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    Notes: Abstract As an alternative to optimum-processor models in which sensors attempt to circumvent internal and external noise, a mechanism-independent argument is presented for Weber's law in vision and hearing. In vision, the argument is that categories of objects should be independent of the light intensity on these objects. In hearing, sound categorization should be independent of the distance from the sound source. An analogous desideratum for computer-based image segmentation is also presented.
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    Bulletin of mathematical biology 45 (1983), S. 193-207 
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    Notes: Abstract Rashevsky's treatment of general binary relations between sets of biological elements is extended using the novel mathematical concept of lattice-valued relation (l.v.r.). This yields a quantitative measure of the strength of the relations between components of a biological organism, and some illustrative examples are given. Specific l.v.r.'s are used to define (more precisely than in Rashevsky's preliminary theory of binary relations) the biologically important relationships amongst hormones, metabolism and energy exchange involved in metabolic reactions. The ‘strongest link’ between the set of hormones and the set of metabolic reactions is quantified using a special l.v.r., and other specific biological realisations of lattice-valued relations in abstract-relational biology are presented. L.v.r.'s may also be regarded as a form ofG-relation in relational biology, or as a particular case of generating diagrams. Further possible developments of this approach, using more complex tools of the newly developed mathematical theory of lattice-valued relations, such as function space l.v.r., group l.v.r., l.v.r. morphisms, l.v.r. homology andn-ary l.v.r.'s are suggested.
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    Bulletin of mathematical biology 45 (1983), S. 259-267 
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    Notes: Abstract The effects of the viscosity-concentration dependence and of the concentration profile on blood flow through a vessel with stenosis have been studied. The flow resistance and the wall shear stress have been found to be smaller than in the two-fluid model with constant viscosities.
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    Bulletin of mathematical biology 45 (1983), S. 507-519 
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    Notes: Abstract A survey is given of branching process type methods in cell kinetics. Some results are given that allow circadian rhythm and do not require complete independence between cells. Some more classical results on balanced exponential growth are given and some comments are made on flow microfluorometry.
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    Bulletin of mathematical biology 45 (1983), S. 439-442 
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    Bulletin of mathematical biology 45 (1983), S. 443-465 
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    Notes: Abstract The spike train activity of neurones is considered as a point process, and methods of analysing and interpreting recorded spike trains are considered. The generation of a continuous process (membrane noise) from interacting point processes is described.
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    Bulletin of mathematical biology 45 (1983), S. 521-554 
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    Notes: Abstract Stochastic models of population genetics are studied with special reference to the biological interest. Mathematical methods are described for treating some simple models and their modifications aimed at the problems of the molecular evolution. Unified theory for treating different quantities is extensively developed and applied to some typical problems of current interest in genetics. Mathematical methods for treating geographically structured populations are given. Approximation formulae and their accuracy are discussed. Some criteria are given for a structured population to behave almost like a panmictic population of the same total size. Some quantities are shown to be independent of the geographical structure and their dynamics are described.
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    Circuits, systems and signal processing 2 (1983), S. 35-44 
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    Topics: Electrical Engineering, Measurement and Control Technology
    Notes: Abstract Via fractional representation methods, this paper tries to clarify the role of various conditions used in the feedback system design and stability with respect to the well-posedness of the system, the existence of a solution for stability and design, and the parameterization of the set of complete solutions. The design criterion for stable feedback system design can be used for filters design, as shown in Section 5. Systems to be considered in this paper include the linear time-varying case and results can easily be extended to the case where systems do not have the same number of inputs and outputs.
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    Circuits, systems and signal processing 2 (1983), S. 57-76 
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    Notes: Abstract Conditions are established which ensure the existence (or non-existence) of limit cycles in feedback systems containing discontinuous elements or elements with hysteresis. The results are applied to a specific example.
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    Circuits, systems and signal processing 2 (1983), S. 45-55 
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    Notes: Conclusion A necessary condition for consistent initial conditions for singular nonlinear systems has been discussed. It is shown that for linear systems or systems of index less than three these conditions are equivlaent to previously reported results. However, for nonlinear systems of index greater than two these new conditions correct those previously reported. One consequence is that Euler's method may fail to estimate solutions for some semi-state equations. R. W. Newcomb's provision of an earlier version of [14] and subsequent correspondence is gratefully acknowledged.
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    Circuits, systems and signal processing 2 (1983), S. 161-177 
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    Notes: Abstract Thep-plane scattering and admittance matrices of SAW transducers consisting ofn equal sections modeled through the hybrid equivalent circuit are explicitly calculated. The results are specialized to the in-line and crossed-field models, and the technique is developed for unequal section transducers.
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    Circuits, systems and signal processing 2 (1983), S. 203-211 
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    Notes: Abstract A set of eight linear spectral transformations which can be used in the design of two-dimensional digital filters is studied from a group-theoretic point of view. Several properties of the transformations, some of them known and some of them new, are deduced and are then applied in the implementation of 2-D digital filters. It is shown that trade-offs exist which can be used to reduce either the amount of memory required for the programming or the amount of data manipulation.
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    Circuits, systems and signal processing 2 (1983), S. 213-238 
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    Notes: Abstract A physically justifiable mathematical model is proposed for a class of current-controlled, negative resistance oscillators having terminal characteristics which are poorly represented by the van der Pol, Scott, and Ceschia-Zecchin equations. Such resonators are typified by the monolithic emitter-coupled astable multivibrator (ECAM). A unique, three-parameter equation, based on the inverse hyperbolic tangent, is matched to the ECAM voltage-current curve. Using the method of Kryloff and Bogoliuboff, the transient and steady-state behavior of the ECAM is derived for oscillation with single-mode and double-mode LCR networks under quasi-linear conditions. An expression for the time of amplitude build-up and decay is derived. A phase plane is constructed for the double-mode case, yielding a system apparently free of simultaneous modes. The validity of the model is experimentally verified for quartz-controlled ECAM devices. The analysis results are extendable ton resonant modes and may be generalized to voltage-controlled devices.
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    Circuits, systems and signal processing 2 (1983), S. 421-443 
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    Notes: Abstract The problem of adaptively detecting two sinusoids corrupted by noise is considered, with emphasis on resolution properties. The approach is to form a spectral estimate from the coefficients of a Δ-step-ahead adaptive predictor. A theoretical analysis reveals that attention to the choice of the prediction horizon Δ gives a distinct improvement in the spectral estimate and in the resolution of the signals. The theoretical results are illustrated with numerical examples. Comparisons with previously suggested techniques are also made.
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    Bulletin of mathematical biology 27 (1965), S. 57-65 
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    Topics: Biology , Mathematics
    Notes: Abstract An outline is given of an analysis that leads to an exact solution for the problem of steady-state diffusion through a finite thick pore into an infinite region surrounding the mouth of the pore. From this exact formula a simple expression for the flux is derived. This expression approximates the flux with a relative error of less than 3.42 per cent independently of the ratiol/a wherel is the length of the pore anda its radius. If desired, more accurate expressions for the flux can be obtained from the exact solution.
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    Bulletin of mathematical biology 27 (1965), S. 79-86 
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    Notes: Abstract The model proposed by A. L. Hodgkin and R. D. Keynes (Jour. of Physiol.,128, 61–88, 1955) for the diffusion of potassium through the nerve membrane is extended to cover an arbitrary number of species of ions with charges not necessarily the same. One type of interference is also investigated.
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    Bulletin of mathematical biology 27 (1965), S. 71-83 
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    Notes: Abstract Most theoretical studies of the circulation have focussed on the transmission line properties of arteries. Only a small number of papers have dealt with the circulation as a closed (lumped) system with two pumps connected by the lesser and greater circulation (Beneken, inCirculatory Analog Computers, No. Holland Publ. Co., Amsterdam, 1963; Defares,et al., inCirculatory Analog Computers, No. Holland Publ. Co., Amsterdam, 1963; Grodins,Quart. Rev. of Biology,34, 93, 1959; Guyton,Cardiac Output and its Regulation, Saunders Publ. Co., New York, 1963). F. W. Cope's recent studies in this journal (Bull. Math. Biophysics,22, 19, 1960;23, 337, 1961;24, 137, 1962) deal with essentially the same questions, although here the circuit is not “closed”. We have attempted to extend the analysis of the areflex (closed) circulation. The complete study is reported elsewhere (Defares,et al., Acta Physiol, et Parmac. Neerl., 1963).
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    Bulletin of mathematical biology 27 (1965), S. 67-78 
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    Notes: Abstract A vector integral equation describing heat distribution within the body has been derived. The factors considered are heat conduction, forced convection via the circulatory system, environmental exchange, metabolic heat production, and change in heat content. The vector partial differential equation and alternative forms incorporating boundary conditions were also developed. A difference equation based on a first-order approximation to the fundamental equations was derived to form the basis of a model for heat distribution within the body. It has been shown that factors involving conduction and convection must be considered independently unless the temperature of the blood flowing from a region of the body is equal to the average temperature of the tissue in that region. If this relation between tissue and blood temperature does exist, only a single temperature from each eleeent is needed to describe the heat distribution. In this latter case, models which ascribe all heat transfer to “equivalent” conduction or to convection can give valid predictions.
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    Bulletin of mathematical biology 27 (1965), S. 87-98 
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    Notes: Abstract It is shown that in a system containingn types of mutually noninteracting binding sites, the association constants are then roots of annth order polynomial while the maximum binding capacities can be evaluated by solving a set ofn simultaneous linear equations. Thenth order polynomial and the system ofn linear equations are defined in terms of 2n intermediate coefficients, the coefficients being themselves evaluated by substituting 2n sets of appropriate experimental data into an auxiliary system of 2n linear equations. The existence and uniqueness of the solutions are established.
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    Bulletin of mathematical biology 27 (1965), S. 111-111 
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    Bulletin of mathematical biology 27 (1965), S. 113-113 
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    Bulletin of mathematical biology 27 (1965), S. 99-109 
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    Notes: Abstract A kinetic theory of ion transport across cell surfaces has been developed in a form analogous to the kinetic theory of electron transport across solid-liquid interfaces of biological particles. The ionic theory is based on the observation that, at least in one instance, the voltage-current behavior for ion conduction across a cell surface is describable by the Tafel equation, in analogy to the conduction of electrons across solid-liquid interfaces. The theory predicts that the kinetics of ion transport across cell surfaces should conform to the Elovich rate equation, which is shown to be true for various experimental data.
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    Bulletin of mathematical biology 27 (1965), S. 114-114 
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    Bulletin of mathematical biology 27 (1965), S. 115-115 
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    Bulletin of mathematical biology 27 (1965), S. 3-4 
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    Bulletin of mathematical biology 27 (1965), S. 5-10 
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    Bulletin of mathematical biology 27 (1965), S. 11-14 
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    Notes: Abstract The present note consists of two separate but related parts. In the first, a new graphtheoretic proof is presented that an (ℳ,R)-system must always contain a nonreestablishable component. The second considers some questions concerning the relation between re-establishability and the time-lag structure in (ℳ,R)-systems. It is supposed that the reader is familiar with the terminology of the author's previous work on (ℳ,R)-systems, particularly R. Rosen,Bull. Math. Biophysics,20, 245–260, 1958.
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    Bulletin of mathematical biology 27 (1965), S. 21-37 
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    Notes: Abstract A simplified, linearized model of the system regulating blood-glucose concentrations is reviewed. This model, which predicts a damped sine wave response to an oral glucose load, lumps the large number of kinetic parameters into a much smaller number which can, at least in part, characterize the human glucose regulatory system. The predictions based on the model are compared with measurements of blood-glucose and blood-insulin concentrations during the oral glucose-tolerance test. Various other conditions are simulated and their implications are discussed in terms of the mathematical model used.
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    Bulletin of mathematical biology 27 (1965), S. 15-19 
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    Notes: Abstract The notion of a compartment is discussed in terms of the Markovian process. From the stochastic matrix (the elements of which are state transition probabilities between different states of a particle of a chemical element), one may find a (generally) nonstochastic matrix; the elements of this second matrix are probabilities that, starting from some initial state, the particle will reach another seleced state (W. Feller, 1962,An Introduction to Probability Theory). Forming equivalence classes of states it can be shown that the equivalence classes based on an equivalence relation, which holds for the elements of the above-mentioned nonstochastic matrix, are essential for the notion of a compartment. From this procedure it is also obvious that a rigorous definition of a physically realizable compartment is impossible. Some conclusions on the practical use of compartmental analysis are drawn.
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    Bulletin of mathematical biology 27 (1965), S. 39-48 
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    Notes: Abstract In a population of cells labeled with a single injection of tritiated thymidine at timet=0, it is assumed that a constant fraction, 1−z, of the cells which are potentially able to divide fail to do so, and that the cells which do divide all have identical generation time,D. Death and emigration of cells are neglected. In mitosis, the partitioning of label among the two daughter cells is supposed to follow the binomial probability law. Using the formalism developed by H. Von Foerster the fraction of labeled cells in the total population is computed as a function oft, the time after injection of label. Ift is an integral multiple ofD the results coincide with those of S. A. Tyler and R. Baserga.
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    Bulletin of mathematical biology 27 (1965), S. 151-160 
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    Notes: Abstract A society with a dominance relation is considered to be built up by starting with a small society and adding new members in succession. As each member is added he engages in contests with each of the older members to determine the dominance relation between them. The probability that the older member dominates is considered to depend on the size of the society and linearly on the older members score. A recurrence relation for the hierarchy index is derived. The approach of the society to a hierarchical structure is considered for various special cases of this probability. Reasonable assumptions concerning this dominance probability are shown to lead to structures close to the hierarchy. If the new member dominates all the older ones below a certain rank, and is dominated by all those above this rank, then the hierarchy will persist if it is the initial structure, or the structure will tend to hierarchy as the size increases, if it is not the initial structure.
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    Bulletin of mathematical biology 27 (1965), S. 183-190 
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    Notes: Abstract The transport of oxygen in a hemoglobin-saturated medium is theoretically investigated using classical transport theory. It is found that all the chemical complexes can be expressed as a single function of oxygen pressure. A potential difference together with apH shift is predicted to occur across the medium.
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    Bulletin of mathematical biology 27 (1965), S. 203-214 
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    Notes: Abstract Several physical effects (magnetomotive force on ions, magnetic induction of electrical field, magnetic changes of inductance) are quantitatively analyzed in an attempt to attain an insight on how externally applied static magnetic fields influence the activity of the neuron and the Nervous System as a whole or in part. The possible magnetic action on shifting excited zones of the axon appears as most promising for prediction and interpretation of measurable effects. Magnetic fields may modify nervous functions by multiplication and addition of very small biophysical effects.
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