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  • Springer  (80,900)
  • 1980-1984  (44,784)
  • 1970-1974  (36,116)
  • 1925-1929
  • 1983  (44,784)
  • 1972  (36,116)
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  • 1980-1984  (44,784)
  • 1970-1974  (36,116)
  • 1925-1929
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  • 1
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    Bulletin of mathematical biology 34 (1972), S. i 
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  • 2
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    Bulletin of mathematical biology 34 (1972), S. 53-63 
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    Notes: Abstract A stochastic model is developed for a compartment with a single time-dependent input, and generalized to include inputs from several sources. With the number of particles of a given molecular species in the compartment as the random variable, the mean, variance and third central moment of this variable are calculated from its generating function, and compared with previous results. The behavior of the calculated moments is discussed, and the possibility of applying the model to chemical and biological systems is considered.
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  • 3
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    Bulletin of mathematical biology 34 (1972), S. 439-441 
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    Notes: Abstract It is shown that from the definition of organismic sets (Rashevsky,Organismic Sets. Some Reflections on the Nature of Life and Society, Holland, Michigan, Mathematical Biology, Inc. and Grosse Pointe, Michigan, J. M. Richards Laboratory) a complete sensory deprivation of an organismic set of ordern=2 should result in malfunctioning of the set. A generalization to higher order sets is suggested.
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  • 4
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    Bulletin of mathematical biology 34 (1972), S. 431-438 
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    Notes: Abstract Optimality in branching structure of the vascular tree was studied. Analysis on its physiological roles as the duct system for blood supply to the capillaries predicted that the vascular tree should be constructed with minimum volume under restriction of determinant pressure, flow and location at the origin and the terminals. Mathematical derivations of this conditional extremum problem yielded some equations expressing the relations between the radii of the branches and their branching angles, which provided numerical solutions for branching points of bi- and poli-terminal minimum volume trees. Comparison of the peritoneal vascular tree in a dog with the minimum volume one computed under the same restrictive conditions showed good agreement in their branching structure.
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  • 5
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    Bulletin of mathematical biology 34 (1972), S. 443-456 
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    Notes: Abstract In order to determine the kinetics of passage of a substance through an organ containing a tangle of vessels, we study the response of a tube to various inflows (perfusion, brief injection, ...). The introduction of the catabolic terms and of the spatial dependence between bulk concentration and surface concentration allows one to account for the difference of arteriovenous concentrations observed experimentally for many metabolites. The relationships between the physico-chemical parameters of the organ and the operational parameters of the model demonstrate the importance of the transit time through the considered vessels. If one considers the different pathways as independent, the introduction of the transit time distribution for an inert substance enables one to compute the response of the organ analytically or by recurrence, using convolution. The parameters of the model can be obtained by the moments method.
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  • 6
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    Bulletin of mathematical biology 34 (1972), S. 457-466 
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    Notes: Abstract The solution of the diffusion equation in the gas phase of the human lung is very difficult because of the structure of the bronchial tree. It is shown by means of physical arguments, how one can reduce the diffusion equation to a simple one-dimensional form. The solution is then obtained by a stochastic simulation, which is easily realized on a digital computer.
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  • 7
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    Bulletin of mathematical biology 34 (1972), S. 467-481 
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    Notes: Abstract A new mathematical model of the oscillatory behavior of the respiratory center has been developed based upon published records of neuronal activity during respiration in the pons and medulla. In contrast with a previous model, four, rather than two, networks are assumed to interact in the respiratory center so as to produce the respiratory oscillation. A mathematical description of this interaction, in the form of a set of four first-order, nonlinear, coupled differential equations, is derived; the behavior of the solutions of this system is studied qualitatively, and expressions for the durations of the inspiratory and expiratory phases are obtained in terms of some parameters. It is found that central and chemical influences drive the medullar neurons to a position somewhere between saturation and full cutoff, and the pontine neurons deeply into cutoff. The control of the duration of the different phases by these chemical and central means is discussed. In order to effect a decrease in the magnitude of the various times, the neurons have to be driven towards operating points of higher central facilitation.
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  • 8
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    Bulletin of mathematical biology 34 (1972), S. 483-502 
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    Notes: Abstract In vivo control of calcium is analysed under the assumption that hormonal influences via plasma levels of parathormone and calcitonin are of prime (but not absolutely dominating) importance. A brief review concerning the physiological significance of body calcium and the mode of action of these two hormones is presented as an introduction to the basic philosophy of the study. A theoretical quasi-linear lumped-parameter model is developed to describe variations in ionic calcium, parathormone and calcitonin plasma concentrations to specific input stimuli. Formal evaluation of the system response requires the determination of ten constants, together with quantitation of ingested calcium entry into the plasma compartment which isindependent of hormonal influences. Values for various parameters are deduced from published data and experimental procedures are outlined to facilitate determination of the remaining unknowns. It is suggested that the proposed model should prove useful for investigations concerning general hormonal actions on calcium homeostatic mechanisms in both normal and diseased states, with particular reference to calcitonin.
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    Bulletin of mathematical biology 34 (1972), S. 521-532 
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    Notes: Abstract Ann species predator-prey chain is analyzed to determine what oscillations occur in population sizes. It is found that only the populations of the first and second species in the chain must necessarily oscillate around the point of equilibrium if they do not come to equilibrium. The other species may or may not oscillate.
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  • 10
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    Notes: Abstract Sangren and Sheppard developed a mathematical model for first-order processes taking place in the regional circulation, applicable—for example—to tracer studies of potassium transport. It permits calculation of specific activity at any point along a “tube of flow” or in the cuff of tissue surrounding it as a function of time following a spike injection of tracer. In efforts to relate to the exchange a rate curves obtained within vivo counters pointed at the region of interest, we developed a compartment-system model of the process. In investigating the properties of the Sangren and Sheppard model integrated over an entire circulatory bed, as thein vivo counter would see it, we found that when the distribution of transit times of the “tubes of flow” can be approximated by an exponential sum, the solution reduces to that of the compartment system model. This results in an important simplification in the calculation, and insight into the assumptions underlying the two different models. A curve-fitting computer program for the compartment model has been written and applied to double-isotope studies of potassium transport in the hind leg of the dog.
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    Bulletin of mathematical biology 34 (1972), S. 547-558 
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    Notes: Abstract Two chemicals,A andB, are allowed to diffuse together and a reaction described by $$A + B\mathop \rightleftharpoons \limits_{K_{ - 1} }^{K_1 } C$$ is allowed to proceed. This system is described mathematically by a system of partial differential equations. A numerical procedure is presented to find the rate constants ofK 1 andK −1. A systematic analysis of the effects of errors is also presented.
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  • 12
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    Bulletin of mathematical biology 34 (1972), S. 533-546 
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    Notes: Abstract Equations are developed to describe the energy expenditure of the human heart. As well as the external potential and kinetic energy terms, general consideration is given to other possible avenues of energy consumption. Emphasis is placed upon using mathematical variables which are readily available for experimental verification. The errors involved in assuming that mean values for the physiological parameters give reasonable estimations for the external mechanical performance are examined, and a theoretical estimation for the discrepancy in the kinetic component is presented. Logical extension of the mathematical derivation leads to a determination of cardiac external mechanical efficiency and clearly demonstrates the significance of the ventricular pressure-volume loop in this context. Finally, experimental procedures are suggested to clarify further some of the conclusions reached through the theoretical analysis.
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    Bulletin of mathematical biology 34 (1972), S. 559-563 
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    Notes: Abstract The question is discussed as to the reason why some animal societies, such as bees or ants, are sexually differentiated, that is, onlysome of its members are exhibiting reproducing activities. It is indicated that human society may be on its way to such a sexual differentiation which may eventually come.
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  • 14
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    Bulletin of mathematical biology 34 (1972), S. 565-565 
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  • 15
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    Bulletin of mathematical biology 34 (1972), S. 567-567 
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  • 16
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    Bulletin of mathematical biology 45 (1983), S. 287-293 
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    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 
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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 
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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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  • 19
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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 
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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 
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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 
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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 
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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 
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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 34 (1972), S. 173-204 
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    Notes: Abstract As a further attempt to determine the stresses and strains of the individual myocardial fibers, the heart muscle is considered as an orthotropic material. A theory is presented which leads to the expression of the equilibrium conditions for the left ventricle in the form of three simultaneous differential equations. Solution of these equations would give the changes in shape of the left ventricle throughout the cardiac cycle, and, in addition, the stresses and strains of the individual myocardial fibers. It is pointed out, however, that meaningful solutions of the equations cannot be obtained at the present time because of difficulties in experimental determination of certain parameters.
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    Bulletin of mathematical biology 34 (1972), S. 213-222 
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    Notes: Abstract This paper compares two previously published neural models for epilepsies (Bull. Math. Biophysics,33, 539–553, 1971;34, 71–78, 1972). The second model is developed in more detail and an attempt is made to bring it more in line with established neurological findings. The question of classification of some epilepsies is briefly discussed.
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    Bulletin of mathematical biology 34 (1972), S. 223-230 
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    Notes: Abstract A formal mathematical model is proposed for a spontaneously repetitively firing neuron. It is based on the assumption that an excitatory and inhibitory substance, possibly different from those involved in synaptic transmissions, is formed in the soma of everynormal neuron. Furthermore, the decay of the substances is ascribed to their combination with some other substances, present in healthy individuals. A generalized two factor system of differential equations is used. It is shown that when the normally present substances are absent, possibly due to genetic defects so that the decay constants become zero, the equations lead to undamped sinusoidal solutions of the difference between excitatory and inhibitory factors, thus producing a trulyspontaneous repetitive discharge, in the absence of external currents or other stimulation. It is suggested that convulsants may act by destroying the substances present in healthy individuals. It is further suggested that by administering to epileptics those substances, which are present in normal healthy persons, perhaps by using brain extracts fromhealthy higher animals which sometimes suffer from epilepsy, an actual cure rather than symptomatic treatment by anticonvulsants may be obtained.
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    Bulletin of mathematical biology 34 (1972), S. 277-291 
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    Notes: Abstract The general kinetic behavior of a multicompartment system is shown to depend upon certain general structural features, including its connectivity, whether it is open, and whether it contains cyclic pathways. Structural influences are clarified by putting the system matrix in a certain form. For systems not strongly connected, a distinction is drawn between partially and completely open systems. Necessary and sufficient conditions are given for non-singularity of the system matrix and for asymptotic stability of the system. Sufficient conditions are given for non-overshooting and monotonic transitions. A system is demonstrated whose solution may contain a prolonged series of damped oscillations; but the oscillations are very slow and small; and it seems unlikely that oscillations could be detected experimentally in any biological system.
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    Bulletin of mathematical biology 34 (1972), S. 243-275 
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    Notes: Abstract It is shown how the fundamental laws of chemical kinetics for either open or closed systems with an arbitrarily large number of reactants can be represented as a system of Riccati-like differential equations. Through the use of a concise tensor notation, it is shown when and how the differential system is exactly reducible to linear form, a reduction without approximation that parallels the well-known similar reduction of a single simle Riccati equation. An example is worked out to show how open kinetics can lead to oscillatory chemical concentrations of the Change-Higgins type. The biologically central problem of great chemical speciation is discussed from the viewpoint of Gibbs ensemble theory within the linearized kinetics and, approximately, within the starting nonlinear kinetics where it is shown roughly how to estimate, from an overall temperature-like parameter characterizing the whole system, mean chemical levels and mean frequencies of oscillation, and where a gross oscillation of the total mass is estimated in terms of an anharmonic oscillator whose general structure is fixed from the structure of the chemical kinetic laws.
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    Bulletin of mathematical biology 34 (1972), S. 293-296 
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    Notes: Abstract A closed chain of compartments in which there is unidirectional transport between adjacent members can exhibit damped oscillations. For a system ofn equivalent compartments, the value ofn which gives the greatest difference between the first maximum and first minimum isn=11, the difference being 1.57%. The greatest difference between the first maximum value and the steady state value is 4% and is obtained whenn=25. The results are illustrated graphically forn equal to 5, 10, 25 and 100.
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    Bulletin of mathematical biology 34 (1972), S. 297-304 
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    Notes: Abstract This paper is a concrete approach to the problem of the number of the sexes. We try to imagine—on the example of three sexes—the mechanisms which would have to accompany a reproduction with several sexes. We have limited our study to the monohybridism, dihybridism and determinism of the sex.
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    Bulletin of mathematical biology 34 (1972), S. 325-335 
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    Notes: Abstract An analysis of the effect of cilia on fluid transport in tubules is presented. The applicability of the results for the flow rates observed in the ductus efferentes of the male tract is discussed.
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    Bulletin of mathematical biology 34 (1972), S. 305-324 
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    Notes: Abstract The dipole models for steady-state currents in excitable membranes of Arndt, Bond and Roper and of Hamel and Zimmerman are compared by fitting the equations to the data of Gilbert and Ehrenstein. The more complex Hammel and Zimmerman model does not fit the data as well as does the simpler Arndt, Bond and Reper model. When fitting the data, the Hammel and Zimmerman current equation reduces to the Arndt, Bond and Roper current equation because of the values assumed by the parameters. An interpretation is given for the parameter values obtained with the Arndt, Bond and Roper model.
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    Bulletin of mathematical biology 34 (1972), S. 337-341 
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    Notes: Abstract It is shown that, under rather general conditions, it is possible to formally decompose the dynamics of ann-dimensional dynamical system into a number of non-interacting subsystems. It is shown that these decompositions are in general not simply related to the kinds of observational procedures in terms of which the original state variables of the system are defined. Some consequences of this construction for reductionism in biology are discussed.
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    Bulletin of mathematical biology 34 (1972), S. 343-353 
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    Notes: Abstract For a certain class of physical machines, termed “structure-determined,” the problem of self-reproduction can be reduced to the problem of serial message reproduction. Serial message reproduction however presupposes a sort of “open system” constraint. This leads to the principle of pseudo, or exogenously standardized, respectively, self-reproduction. It seems to be consistent with both chemical and biological self-reproduction. It thus may reflect a general principle of biological design. The proposed principle is a physico chemical analog to Robert Rosen's abstract relational self-reproduction constraint.
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    Bulletin of mathematical biology 34 (1972), S. 355-377 
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    Notes: Abstract Equations are derived describing potentials due to an active muscle fiber in an infinite medium in terms of two surface integrals—one of the propagated action potential and the other of the membrane current density, both integrals being taken over the surface of the muscle. These equations are incorporated into an equivalent cardiac current generator in which the left ventricle (i.e. the current source) is represented by a three-dimensional wedge and the thorax (i.e. the volume conductor), by a homogeneous circular cylinder. Since this current generator expresses the body surface potentials in terms of the membrane current density and the membrane potential at any point on the surface of the electrically active muscle fiber, the calculated ECG can be correlated with theactual sources within the heart. This equivalent cardiac generator possesses many of the physical and physiological properties of cardiac muscle. The equations were evaluated numerically on a digital computer. The results indicate that equivalent cardiac current generators of this type can yield clinically significant results and that further research is necessary to investigate their properties fully.
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    Bulletin of mathematical biology 34 (1972), S. 413-418 
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    Notes: Abstract Analytical solutions are presented for transient heat conduction in biological media. General boundary conditions and internal sources varied in both spatial and time variables are considered, thus, solutions for many special cases can be obtained with ease from the general solutions presented in this analysis.
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    Bulletin of mathematical biology 34 (1972), S. 393-412 
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    Notes: Abstract Two mathematical models of pulmonary single breath gas washout (one analytic, one numerical) are developed and their predictions compared with experimental data on human subjects. Weibel's 23 generation symmetric anatomical model is used as a guide to bronchial tree geometry. Experimental plots of nitrogen concentration versus volume expired, dead space versus breath holding time, and dead space versus tidal volume are compared with plots predicted by the models. Agreement is good. A plot of nitrogen concentration in the airways as predicted by the numerical model at different times during inhalation and exhalation of a single breath of oxygen is shown. Model predictions for changes in dead space with changes in washout gas and expiratory flow rate are discussed. Use of the analytic model for obtaining average values of the path length from mouth to alveoli in a given subject is discussed. To the extent of their agreement with experiment, the models provide a sound physical basis for the correlation of airway structure and function.
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    Bulletin of mathematical biology 34 (1972), S. 429-429 
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    Bulletin of mathematical biology 34 (1972), S. 419-427 
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    Notes: Abstract The Roginsky-Zeldovich (or Elovich) equation, which is −dx/dt=m exp (nx) (x=substrate concentration,t=time,m andn=constants), describes the kinetics of various biological electron and ion transport processes, and has been derived from the concept of charge transport across an activation energy barrier at an interface between dissimilar phases, driven by a difference in redox or ion potentials, with the simplifying assumptions that charge carrier concentration is constant, backward current across the interface is zero, and diffusion of substrate is fast. If charge carrier concentration is proportional to substrate concentration, then the kinetic equation is −dx/dt=mx exp (nx). If backward current is not zero, then −dx/dt=m 1 exp (n 1x) −m 2 exp (n 2 x), wherem 1,m 2,n 1 andn 2 are constants. Kinetic equations for interfacial charge transport in the presence of a significant substrate diffusion potential are also derived.
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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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    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 34 (1972), S. 1-12 
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    Notes: Abstract A method is described for estimating cell-cycle parameters from experimental fraction-of-labeled-mitoses measurements. The method is closely related to that of J. C. Barrett (1970) but is based on the analysis of Brockwell and Trucco (1970) which takes into account population growth in the calculation of theoreticalFLM-functions. Several sets of experimental data are analyzed, among them the data for the Marshall tumor considered by Barrett. It is found that population growth has a small but nevertheless detectable effect on the estimates of the cell parameters.
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    Bulletin of mathematical biology 34 (1972), S. 33-44 
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    Notes: Abstract The radioactivity disappearance curves of glucose-6-14C albumin-I131 after a single injection of tracer into a human subject have been determined in detail, particularly at early time intervals. The curves, expressed as sums of exponentials, have been analyzed as the infinite sum of convolutions of single passage time densities. The resultant transfer time distribution of a single circulatory pass allows examination of all delays in the system no matter how long they take. The structural detail evident by this means and the long mean time of a single pass of glucose (〉5 min) supports the thesis that factors other than rapid and uniform diffusion play a role in the extravascular movements of glucose molecules.
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    Bulletin of mathematical biology 34 (1972), S. 13-31 
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    Notes: Abstract A bisexual multiple branching process is studied. Consider a population with respect to three genotypes in both the female and male populations and let $$X(n) = \left\langle {X_1 (n), X_2 (n), X_3 (n)} \right\rangle and Y(n) = \left\langle {Y_1 (n), Y_2 (n), Y_3 (n)} \right\rangle$$ be random vectors giving the number of females and males (respectively) of each genotype in generationn. The mating of females and males is accommodated in the model withZ ij (n) representing the number of females of theith genotype mated with a male of thejth genotype in generationn. The mating system is such that a female may be mated to only one male but a male may be mated with more than one female. By arranging the nine random variablesZ ij (n),i, j=1, 2, 3, in a 1×9, vectorZ(n) it is shown that under certain conditions there is a positive constant ϱ such that when ϱ〉1 the vectorsZ n /ρn,X n /ρn andY n /ρn converge almost surely asn→∞ to random vectors with fixed directions. The paper is divided into four sections. In section 1 the model is described in detail and its potential applications to population genetics are discussed. In section 2, the generating function of the transition probabilities of theZ-process are derived. Section3 is devoted to the study of the limiting behavior of the first and second moments of theZ-process, and in section4 the results of section3 are utilized to study the behavior of the random vectorsZ(n),X(n) andY(n) asn→∞.
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    Bulletin of mathematical biology 34 (1972), S. 45-52 
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    Notes: Abstract Herein we show that the voltage-clamp current density at zero time calculated from electrodiffusion equations is linear in the clamping voltage for a simple membrane (no charge structure) and for a membrae with fixed charges. Such membranes are nonexcitable. Excitable membranes can be represented by a homogeneous membrane with dipole layers at the surface. In this case the initial current density will be linear in the clamping voltage if a critical field for a dipole layer reorientation is not passed through in changing from holding to clamping potential. Otherwise, deviation from nonlinearity may occur. This is in agreement with experimental data for the squid giant axon.
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    Bulletin of mathematical biology 34 (1972), S. 65-69 
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    Notes: Abstract By generalizing a previous paper on periodicities in the endocrine system (Bull. Math. Biophysics,30, 735–749, 1968), it is shown that nonperiodic, sporadic oscillations in the system are also possible. A procedure of describing the feedback mechanism between the endocrine system and the central nervous system is suggested. It is shown that the combined system: endocrine—CNS, also may show sporadic fluctuations.
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    Bulletin of mathematical biology 34 (1972), S. 79-86 
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    Notes: Abstract This paper deals with a mathematical attempt to determine the wall shear during normal flow of blood in the ascending and the descending thoracic aorta. A simple model is used, but the results obtained are in agreement with published experimental results for the descending thoracic aorta. It is suggested that the degree of fluctuation in the pressure gradient at a given station is the major factor in determining the level of wall shear at that point.
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    Bulletin of mathematical biology 34 (1972), S. 71-78 
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    Notes: Abstract A neural model based on a generalization of a model proposed in 1938 in the first edition of the author'sMathematical Biophysics (Chicago: Univ. of Chicago Press) is described. It possesses the property that due to some endogenous or exogenous stimulus, which may be of random nature, a pathway may suddenly begin to fire spontaneously. This spontaneous firing may either gradually spread over other pathways and eventually cease, or it may remain localized within one or a few pathways and then cease. Which of the two types of events occurs depends on the values of a number of parameters. The case of spreading reminds one of Jacksonian epilepsy.
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    Bulletin of mathematical biology 34 (1972), S. 93-102 
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    Notes: Abstract The diffusion equation is solved for a membrane-bounded sphere situated in an infinite medium with different diffusion properties. The formal solution is obtained through Laplace transformation in the time variable. It is not possible to find a closed form solution in terms of analytical functions, and therefore a numerical inversion technique is applied to obtain the final solution. The application on a biological problem is discussed.
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    Bulletin of mathematical biology 34 (1972), S. 87-92 
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    Notes: Abstract It is shown that the individual rate constants can be determined for the composite chemical system: $$A + B_i \rightleftarrows C_i ; i = 1...N$$ with only measurements of the unbound species,A(t), required. The dissociation rate constants can be determined by direct analysis of a single steady state tracer study. The association constants then follow from the analysis of stable equilibrium determinations reported earlier (Hart, 1965). An approximate solution when tracer methods are in-applicable is also given.
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    Bulletin of mathematical biology 34 (1972), S. 103-112 
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    Notes: Abstract Certain arrangements of enzymatic (bimolecular) subsystems lead to characteristic threshold-type response. Two simple cases of such systems are studied here in terms of steady state behavior and explicit relationships between system and curve parameters. It is found that the curvature of the threshold curve is directly related to the equivalent Michaelis constant and, in the case of saturated threshold curve, the slope of the curve at the idealized threshold is limited by the ratio of saturation to threshold. This slope may be appreciably increased up to a stepwise response at the threshold if a multisubstrate complex of the enzyme is the only species which affects the enzyme mediated transport.
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    Bulletin of mathematical biology 34 (1972), S. 113-148 
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    Notes: Abstract Many experimental studies have indicated that the intraocular pressure is subject to mediation by adrenergic mechanisms affecting both the rate of formation of the aqueous humor and the resistance of the pathway through which the aqueous humor flows out of the eye. Thus, for example, the role of adrenergic drugs in glaucoma therapy is well known. How the mediation is accomplished has not been clarified in detail. Several possible mechanisms have been suggested, and all may indeed be involved. The present study is concerned with the basis and mathematical formulation of one of them and the consequences with respect to aqueous dynamics. The analysis leads to expressions for the aqueous outflow resistance and the formation rate, as well as other quantities of interest. The theoretical behavior is shown to compare favorably with the results of infusion studies and various other experiments, and to provide a unified picture of much of the pressure-flow behavior of both the living and the dead eye.
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    Bulletin of mathematical biology 34 (1972), S. 149-150 
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    Bulletin of mathematical biology 34 (1972), S. 151-172 
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    Notes: Abstract Following Wei's suggestion that nerve stimulation and conduction properties are due to dipole layers at the two membrane surfaces (Wei, 1969), we have done steady-state electro-diffusion calculations in the constant field approximation for a simple double-dipole-layer model. We are thereby able to quantitatively fit the recent potassium iso-osmotic rectification curves of Gilbert and Ehrenstein for the squid giant axon membrane. For the squid axon membrane in a natural ion environment, only the outside dipole layer is present in the fit to the data.
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    Bulletin of mathematical biology 34 (1972), S. 205-211 
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    Notes: Abstract In this paper the left ventricle of the heart was considered as a shell of varying thickness. The first and second fundamental forms of the middle surface, of the shell, as well as Euler's theorem were used for deriving expressions giving the length and curvature of the individual myocardial fibers. Recent anatomical studies have shown that the myocardial fibers in the middle of the left ventricular wall follow a course nearly parallel to the horizontal plane (Streeteret al., 1969). In previous papers (Voukydis 1969, 1970) a mathematical description of the curvature and length of the individual myocardial fibers was presented. Unfortunately, both the curvature and the length formulas contained the cotangent of the fiber helix angle, which approaches infinity as the fiber assumes a course parallel to the horizontal plane. Consequently, these two formulas cannot be used for fibers nearly parallel to the horizontal plane. The present paper will give an alternative way for calculating the length and curvature of the individual myocardial fibers, based on the fundamental forms of surface and on Euler's theorem.
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    Bulletin of mathematical biology 34 (1972), S. 231-242 
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    Notes: Abstract It is pointed out that the successes obtained in the mathematical biology of the central nervous system are based mostly on a number of more or less complicated neuronic circuit models, each inventedad hoc for the purpose of explaining a given phenomenon. The individual models remain disconnected from each other, however, and the unity of the CNS is not apparent. (Rashevsky,Mathematical Biophysics, 3rd Edition, Vol. II, 1960. New York, Dover Publications, Inc.) Some “field theories” of the CNS, as for example that of Griffith (Bull. Math. Biophysics,25, 111–120, 1963;27, 187–195, 1965), give more expression to this unity but lose in the explanation of specific phenomena. The present paper starts with the picture thatevery neuron in the brain isdirectly or indirectly affected to some extent byevery other neuron. This leads to a system of equations with a very large number of variables. Such a system can be replaced in the limiting case by an integral equation of the first kind. At least two specific results can be obtained with this approach and suggestions for further improvement are made.
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    Bulletin of mathematical biology 34 (1972), S. 379-392 
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    Notes: Abstract Pressure-volume and volume-dimensions relationships, obtained from excised dog left ventricles were used for calculating the stresses acting along the longitudinal axis of the individual myocardial fibers. The calculations were based on a set of empirical and theoretical equations. The pressure-volume relationship as well as the volume-dimensions relationships for the excised left ventricle were expressed in the form of empirical equations; the fiber orientation was written as a function of the fiber location within the left ventricular wall; finally, the fiber stress was determined by means of theoretically derived formulas. Simultaneous solutions for the fibers of a meridian cut through the left ventricular myocardial shell were obtained by means of a digital computer and presented in the form of diagrams. The results showed that at low degrees of distension of the left ventricle there are two zones of higher stresses at the equatorial area, one near the epicardium and one near the endocardium. As the distension proceeds under the effect of progressively increasing intraventricular pressure, these two zones become less well defined, whereas a new zone of higher stresses appears near the apex. At high degrees of distension, the ventricle assumes a more spherical shape and the equatorial zones of higher stresses are replaced by zones of lower stresses. Increase in the myocardial mass results in appearance of the equatorial lower stress zones at lower degrees of distension.
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    Bulletin of mathematical biology 45 (1983), S. 11-20 
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    Notes: Abstract This paper is concerned with a generalization of the simple epidemic model in which the infective population is partitioned intom classes, each of specific infectiousness. Attention is restricted, however, to the case where all the meeting rates between two individuals are equal to each other. Both deterministic and stochastic versions are examined. In either case the development in time of the epidemic process is investigated by exploiting a connection with the standard simple epidemic model. Finally, it is shown that the technique used also applies to a similar model for the spread of information.
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    Bulletin of mathematical biology 45 (1983), S. 33-40 
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    Notes: Abstract For each rooted binary tree witht labeled terminal vertices (leaves) a natural number can be assigned uniquely. Unrooted trees witht labeled terminal vertices andt-2 unlabeled internal vertices of degree 3 can also be numbered uniquely using the same convention. Rooted trees in which the hights of the internal vertices are rank ordered are also considered. Applications to problems in taxonomy are discussed.
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    Bulletin of mathematical biology 45 (1983), S. 41-50 
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    Notes: Abstract Expressions and numerical values for hematocrit reduction are calculated as blood flows from a cylindrical feeding tube into a cylindrical capillary at a right-angle branch. Blood is considered to consist of two Newtonian fluids, plasma and red cell suspension, which have equal densities but different viscosities. The concentration profile of the red cells is concluded to depend on the size of the feeding tube. An estimate for the thickness of the plasma layer adjacent to the wall is obtained.
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