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  • Springer  (107,655)
  • 1980-1984  (43,712)
  • 1965-1969  (58,742)
  • 1925-1929  (5,201)
  • 1981  (43,712)
  • 1968  (32,184)
  • 1966  (26,558)
  • 1928  (5,201)
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  • 1980-1984  (43,712)
  • 1965-1969  (58,742)
  • 1925-1929  (5,201)
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  • 1
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    Bulletin of mathematical biology 28 (1966), S. 333-345 
    ISSN: 1522-9602
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract This paper is a sequel to a paper by the author entitled “Restricted Transition Probabilities and Their Applications to Some Problems in the Dynamics of Biological Populations” (Bull. Math. Biophysics, 1966,28, 315–331). The paper is divided into two parts. In part one some aspects of the maximum size attained by the population during a finite time interval are studied for the case the stochastic process underlying the evolution of the population is a birth process. Two interesting by-products emerge from the study presented in part one; namely a combinatorial method of finding solutions to the Kolmogorov differential equations in special cases, and secondly, a set of criteria for the optimum allocation of genotypes in the host population of a host-pathogen system. The optimum allocation of genotypes in the host population is a problem of practical importance in controlling plant pathogens. In part two the theory of restricted transition probabilities developed in the companion paper is applied in finding the distribution of the time to the appearance of the first mutation for the case of a two dimensional birth process. The distribution of the time to the appearance of the first mutation is of importance in understanding the role mutation plays in the evolution of a population, particularly in the pathogen population of a host-pathogen system.
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  • 2
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    Bulletin of mathematical biology 28 (1966), S. 355-362 
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    Notes: Abstract The complex arrangement of the muscle fibers in the ventricular wall and the nonsymmetric contraction and expansion of the ventricle preclude the writing of a differential equation of motion for the ventricle as a whole. We can, however, describe the motion of the ventricle by describing the motion of the dimensional parameters length and diameter; the radius, circumference, cross-sectional area, and volume following naturally from these. The ventricle is assumed to be an ellipsoid of revolution and the dimensional parameters to be periodic functions of time. Each of the parameters is expressed as a Fourier series.
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  • 3
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    Bulletin of mathematical biology 28 (1966), S. 347-354 
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    Notes: Abstract Le modèle de Nelson peut-être considéré comme une approximation du modèle de Hodgkin-Huxley. Moins précis, il est plus maniable. Le modèle de Nelson peut également être considéré comme une généralisation du modèle de Hodgkin-Huxley. En effet, il introduit des liaisons synaptiques localisées ou diffusantes, et un processus de facilitation. Le mécanisme des liaisons synaptiques ne se traduit pas facilement dans le langage de Hodgkin-Huxley. Par contre, le processus de facilitation s'interprète facilement. Nelson's model can be taken as an approximation of Hodgkin-Huxley's model. Its precision is lesser, but it is more usable. Nelson's model can also be taken as a generalization of Hodgkin-Huxley's one; for it introduces localized or diffusing synaptic connexions and a facilitating process. The mechanism of synaptic connexions cannot be easily translated into Hodgkin-Huxley's language. On the contrary, the facilitating process is easily interpreted.
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    Bulletin of mathematical biology 28 (1966), S. 363-370 
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    Notes: Abstract A spherical model for the human left ventricle with two different types of aneurysms, circular and rectangular-square, is proposed and meaningful relations are derived between the parameters of the aneurysms and ventricle. Such ventricular parameters as stroke volume, end-diastolic volume, and end-systolic volume are given normal human values to compute values for end-systolic radius and percentage shortening of muscle for various sized circular and rectangular-square aneurysms.
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  • 5
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    Bulletin of mathematical biology 28 (1966), S. 375-378 
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    Notes: Abstract The Volterra theory of two competing populations is extended to the contemporary social problem of crime control. Domains of stability for the time dependence of the numbers in the criminal and enforcement groups are exposed by a numerical example. Both augmentation and reduction of enforcement can produce a stable system. Average values of the ratio of members in each group show great sensitivity to the control policies adopted by the remaining sector of the total population.
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    Bulletin of mathematical biology 28 (1966), S. 379-390 
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    Notes: Abstract The paper deals with interactions of substances via an enzymatic reaction (Bull. Math. Biophysics,25, 141–154, 1963). The substances are the activators, inhibitors and/or substrates of the reaction. Due to the bimolecularity of the processes in the reaction, the quantitative relation between the steady state amount of complexes and the amounts of the substances assumes a typical form. In multiple enzymatic reactions this form is more complicated, though basically similar. Because the substances may influence the steady state amounts of the complexes in opposite directions, the compensation and blocking effects are the properties of enzymatic reactions. The substances with the same direction of influence may potentiate each other. In the enzymatic reaction here considered, the potentiation is always non-negative.
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    Bulletin of mathematical biology 28 (1966), S. 391-409 
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    Notes: Abstract Growth-rate functions in analytic form have been obtained for cell cultures in which the doubling times follow the Gaussian and Poisson distributions. The growth-rate functions are calculated by using Laplace transforms to solve an integral equation previously presented. Oscillatory solutions result if a substantial fraction of the cells in a culture are synchronized to divide at some particular time. The synchrony and, hence, the oscillatory character of the growth-rate function eventually disappear because of the non-zero variance of the doubling-time distribution. If their variances are sufficiently small, the Gaussian and Poisson doubling-time distributions lead to growth-rate functions that become identical in the limit of large time.
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    Bulletin of mathematical biology 28 (1966), S. 411-416 
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    Notes: Abstract IfN(t) is the expected number of cells in a culture at timet, $$\dot N(t)$$ the corresponding time derivative, andf(t−τ)dt the probability that a cell of aget−τ at timet will divide in the succeeding time intervaldt, then according to Hirsch and Engelberg (this issue) there obtains the integral equation $$\dot N(t) = 2\int_{ - \infty }^t {f(t - \tau )\dot N(\tau )d\tau }$$ for describing the dynamics of the cell population. It is the purpose of this note to give two alternative derivations of this equation, one based on the age density equation of Von Foerster, and the other based on a generalized form of the Harris-Bellman equation describing the first moment of an age dependent, branching process. In addition, a probability model is posed from which the Von Foerster equation and, hence, the Hirsch-Engelberg equation readily follows.
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    Bulletin of mathematical biology 28 (1966), S. 417-432 
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    Notes: Abstract A model of the dissolution kinetics of powdered enamel is developed based on the kinetic rate termq, $$q = K'H - k'C \cdot P_1$$ , whereH=[H +],C=[Ca ++] andP 1=[HPO 4 = ]. The differential equations describing the rate of mineral dissolution (and the linearly related rate of appearance of calcium and phosphate in solution) have been derived and solved for three basic cases: (1) when thepH of the solution and surface area of the enamel are considered constant, (2) when thepH is assumed constant, but the reduction in surface area during dissolution is considered, and (3) when the rise ofpH resulting from the buffering effect of the dissolved enamel is considered along with the change in surface area. Analytical solutions have been obtained for cases (1) and (2), while a numerical solution has been found for case (3). Data from a study on enamel dissolution are presented that agree with the theory of case (3), and it is noted that apH rise as large as 0.5 can occur, as has been shown elsewhere in the literature.
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    Bulletin of mathematical biology 28 (1966), S. 477-481 
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    Notes: Abstract On the basis of Landahl's theory of two-choice learning it is shown that application of punishment for wrong responses, without giving award for correct ones, does not lead to complete learning, no matter how many trials are used. If initially a “wrong response” was learned, then an attempt to inhibit it by punishment alone will in a class of cases lead only to a 50% suppression of that wrong response. Possible connection with the problem of effectiveness of punishment as a deterrent for crime is mentioned.
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    Bulletin of mathematical biology 28 (1966), S. 483-483 
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    Bulletin of mathematical biology 28 (1966), S. 483-483 
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    Bulletin of mathematical biology 28 (1966), S. 485-485 
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    Bulletin of mathematical biology 28 (1966), S. 501-510 
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    Notes: Abstract A set of characteristic parameters is given for electrophoresis accompanied by diffusion, followed by a method of simplification of the transport equation. The concept of electrophoretic similarity is introduced in connection with the presentation of solutions and the final section contains some dimensional considerations of the potential equation.
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    Bulletin of mathematical biology 28 (1966), S. 511-517 
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    Notes: Abstract We show that when we represent (ℓ, ℛ)-systems with fixed genome as automata (sequential machines), we get automata with output-dependent states. This yields a short proof that ((ℓ, ℛ)-systems from a subcategory of automata—and with more homomorphisms than previously exhibited. We show how ((ℓ, ℛ)-systems with variable genetic structure may be represented as automata and use this embedding to set up a larger subcategory of the category of automata. An analogy with dynamical systems is briefly discussed. This paper presents a formal exploration and extension of some of the ideas presented by Rosen (Bull. Math. Biophyss,26, 103–111, 1964;28, 141–148;28 149–151). We refer the reader to these papers, and references cited therein, for a discussion of the relevance of this material to relational biology.
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    Bulletin of mathematical biology 28 (1966), S. 487-500 
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    Notes: Abstract A two-dimensional nonlinear integro-differential equation with time-varying coefficients describing the behavior of the fluttering wing-body systems typical of natural flight mechanisms has been deduced from the Navier-Stokes equation which generalizes local pressure and velocity distributions in the externally oscillating air field. The resulting equation for the wing forces is combined with an analogous expression for the forces of gravitation and acceleration associated with the body. The air acceleration force, not previously considered in bio-physical models of insect and bird flight, is shown to arise from a formal analysis of unsteady or time-varying contributions to the velocity field, while the square form of the conventional steady state aerodynamic forces is derived from the intertial terms in the Navier-Stokes equation with the aid of the approximations of Newtonian impact theory. Previous calculations (Houghton, 1964) have indicated that the contribution to gravitational stability of air acceleration and aerodynamic life are roughly in the ratio of 3:1.
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    Bulletin of mathematical biology 28 (1966), S. 519-536 
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    Notes: Abstract Certain types of cortical electrical events are non-propagated so that the associated electric fields must have standing wave characteristics. However, cortical electric events typically are generated by neurone populations which cannot be activated simultaneously on impulse driving. Hence the sum of the standing wave fields due to asynchronous activation of adjoining regions of cortical neurones must give the appearance of a traveling wave. Analysis of cortical waveforms is further complicated by curvature in cortical surfaces. A model is presented that shows the effects of curvature and time lag in activation on the form of the potential at points in space around a laminar array of elements simulating a population of cortical neurones. The results are compared with waveforms evoked by single-shock stimulation of the prepyriform cortex in cats.
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    Bulletin of mathematical biology 28 (1966), S. 545-554 
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    Notes: Abstract A continuity equation for cell-number density in a population of cells is derived, and a system of equations for eliminating parameters between the general solution and the initial distribution obtained.
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  • 19
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    Bulletin of mathematical biology 28 (1966), S. 537-544 
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    Notes: Abstract Use of an electrical model of the left ventricle of the heart and the arterial system permits analysis of the changes which take place as the capacity of the myocardium for generation of force decreases. The model is simple in structure, and its construction and practical testing would not be difficult. It demonstrates that, as the heart muscle weakens, the peak of intracardiac force occurs later in systole, and the difference between the intracardiac pressure and the aortic pressure in the second half of systole is much greater than for the normal heart. The feedback mechanisms which are proposed to affect myocardial contractility would affect this compensation for cardiac weakening. Indices to categorize the behavior of the normal, compensated though weakened, and decompensated myocardium are proposed.
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    Bulletin of mathematical biology 28 (1966), S. 555-566 
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    Notes: Abstract The frequency distribution in a population of cells of the quantityCD (defined as the amount of some chromosomal substance in a cell which containsC chromosomes) is calculated using the distribution in the population of the amount per chromosome,D, and the distribution of chromosome number,C.
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    Bulletin of mathematical biology 28 (1966), S. 567-574 
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    Notes: Abstract The rate of chromosomal DNA synthesis in an exponentially growing population of cells having chromosome-number dispersion is calculated using DNA histogram data, chromosome-number distribution data, and the assumptions that the synthesis rate is constant and DNA double exactly.
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    Bulletin of mathematical biology 28 (1966), S. 575-584 
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    Notes: Abstract An estimate is made of the rate coefficient for linear DNA synthesis with exact doubling in an exponentially growing population of Ehrlich ascites tumor cells having chromosome-number dispersion. Comparison of calculated and experimental results suggest that the assumptions used in the calculation are tenable, but further experimental evidence is needed to prove this.
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    Bulletin of mathematical biology 28 (1966), S. 655-661 
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    Notes: Abstract The paper develops further some suggestions made previously (Bulletin of Mathematical Biophysics,28, 283–308, 1966) that certain biological phenomena may be more easily interpreted from a “sociological” point of view by considering the organism as a social aggregate of cells and a cell as a social aggregate of genes. In this light the problems of origin of life on earth, of aging, and of parasitism and symbiosis are discussed. The notion of social aggregates of different orders is introduced.
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    Bulletin of mathematical biology 28 (1966), S. 663-663 
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    Notes: Abstract A theoretical and experimental study was made of the mechanical behavior of the cornea. The theoretical analysis included an analytical solution for the symmetrical constraint of a thin, shallow, spherical shell by a rigid indenter. The experimental study investigated the rheology of the cornea with particular emphasis on its compliance with the requirements of the Boltzmann Superposition Principle. Representative results of tests on twenty enucleated hog eyes and two human eyes have been reported. The corneas of the human and hog eyes behaved as linear viscoelastic solids; the human eyes differed from the hog eyes in having a long term creep component. Several eyes were tested at the site of procurement, six to seven minutes after the animal's death, and it was established that creep is not an artifact due to aging or enucleation. The analytical and experimental results were combined to study some instruments used to detect the level of pressure in the eye. The theoretical analysis predicted that a type of elastic instability occurs during the process of flattening a small portion of the cornea; this is discussed with reference to the Goldmann and Mackay-Marg tonometers. The role of corneal creep was considered with reference to the response of the Schiøtz indentation tonometer during the time dependent process known as tonography.
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    Bulletin of mathematical biology 28 (1966), S. 645-654 
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    Notes: Abstract Following previous studies, differential equations are established which determine the variation of the stimulus towards a corrective turn of the steering wheel and its effect on the excitation of the centers in the brain which results in the production of the corrective turn. The equations are derived under the highly oversimplified assumption that all excitation thresholds are so small that they can be neglected. Under these assumptions it is found that the tracking curve of a car is a sinusoid with negative damping, that is, with an ever increasing amplitude. Driving under these assumptions is imposible since the car will always eventually jump off the road. The possible effects of the threshold as well as stimuli towards corrective turns other than the distance from the edge of the lane are very briefly discussed. In spite of the negative results of the paper, its interest lies in the circumstance that with the complication of the model, we find that driving depends not only on the reaction times as the only “purely biological” parameter, but on three other neurobiophysical constants. In a subsequent paper (Rashevsky, 1967) it is shown how the introduction of one or more purely biological parameters of the driver makes a stable driving regime possible.
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    Bulletin of mathematical biology 28 (1966), S. 663-663 
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    Bulletin of mathematical biology 43 (1981), S. 1-19 
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    Notes: Abstract By studying the behavior of various tracer species in the lungs, one can assess many important characteristics which distinguish normal and abnormal function. Quantitative evaluation of function depends on the use of an appropriate model in conjunction with experimental data. A multi-compartment model is derived from mass balances to describe dynamic as well as (breath-averaged) steady-state transport processes between the environment and pulmonary capillary blood. The breathing cycle is divided into three time periods (inspiration, expiration, and pause) so that the model equations are discrete in time. No other model of tracer species transport in the lungs deals simultaneously with species dynamics, variable breathing pattern, distribution inhomogeneities, and non-equilibrium between alveolar gas and capillary blood. Models currently in the literature are shown to be special cases of the model presented here.
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    Bulletin of mathematical biology 43 (1981), S. 47-58 
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    Notes: Abstract Local stability seems to imply global stability for population models. To investigate this claim, we formally define apopulation model. This definition seems to include the one-dimensional discrete models now in use. We derive a necessary and sufficient condition for the global stability of our defined class of models. We derive an easily testable sufficient condition for local stability to imply global stability. We also show that if a discrete model is majorized by one of these stable population models, then the discrete model is globally stable. We demonstrate the utility of these theorems by using them to prove that the regions of local and global stability coincide for six models from the literature. We close by arguing that these theorems give a method for demonstrating global stability that is simpler and easier to apply than the usual method of Liapunov functions.
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    Bulletin of mathematical biology 43 (1981), S. 125-140 
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    Notes: Abstract The asymptotic behaviour of a logistic equation with diffusion on a bounded region and a diffusionally coupled delay is investigated. An equivelent parabolic system is derived for certain types of delays. Using a Layapunov functional, sufficient conditions for the global asymptotic stability of the constant steady state are obtained. When the global stability is lost, using Hopf's bifurcation theory, existence of travelling waves is shown for ring-like and periodic one dimensional habitats.
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    Bulletin of mathematical biology 43 (1981), S. 141-149 
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    Notes: Abstract It was hypothesized in an earlier work that sensory perception can occur only when the perceiving system is uncertain about the nature of the event being perceived. In the absence of any uncertainty, perception will not take place. The response of the sensory afferent neuron (impulse transmission rate) was calculated using Shannon's measure of uncertainty or entropy. It will now be shown that when the event being perceived is the position and momentum of a particle, Shannon's measure of uncertainty leads to the Heisenberg Uncertainty relationship.
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    Bulletin of mathematical biology 43 (1981), S. 239-244 
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    Notes: Abstract It is not unusual for several classifications to be given for the same collection of objects. We present a method, called majority rule, which can be used to define a consensus of these classifications. We also discuss some mathematical properties of this consensus tree.
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    Bulletin of mathematical biology 43 (1981), S. 259-270 
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    Notes: Abstract The dependence of the spatial concentration profiles of morphogens on a characteristic dimension is obtained by continuation techniques for Gierer and Meinhardt's activator-inhibitor model of morphogenesis. The study of the behaviour of the system during growth, where the linear and exponential increase of the characteristic dimension is considered, revealed that more complex patterns of morphogen spatial concentrations appear regularly in a reproducible way.
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    Bulletin of mathematical biology 43 (1981), S. 271-278 
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    Notes: Abstract Computer models have been used by various authors to simulate both the growth of normal cellular tissue and the development of cancerous cells within normal tissue. As these models were the result of considerable idealization, the purpose of the present paper is to propose a model in which the degree of simplification is relaxed: the features of simultaneous growth, and cell growth whose rate depends on the free absorbing periphery of the cell are introduced. Simulation experiments have been conducted using the model, and the results are presented.
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    Bulletin of mathematical biology 43 (1981), S. 341-346 
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    Notes: Abstract The theory of complementary variational principles is used to obtain maximum and minimum principles for a nonlinear model of heat conduction in the human head. Accurate variational solutions are obtained in illustrative calculations. The effect of nonlinearity is seen to be significant from a comparison with the linearized model.
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    Bulletin of mathematical biology 43 (1981), S. 279-325 
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    Notes: Abstract A model for the nerve impulse due to Zeeman (1972) and based on catastrophe theory is compared with alternative models and criticisms of Zeeman's model by Sussmann and Zahler (1977, 1978) are assessed. The criticisms of Zeeman's motivation for his model are found to carry some weight. Sussmann and Zahler (1977, 1978) list numerous features of Zeeman's model which, they state, are not in agreement with experiment. These statements as they stand are largely erroneous, and the model still remains to be tested by a critical series of experiments. However, a detailed analysis reveals defects in Zeeman's model, not among those claimed by Sussmann and Zahler, showing that the explicit equations of the model cannot be correct. The possibility of a modified approach along similar lines and its ultimate adoption remains open.
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    Bulletin of mathematical biology 43 (1981), S. 375-388 
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    Notes: Abstract The irreversible Michaelis-Menten reaction is studied by the use of the method of multiple scales. Three stages of the reaction are identified, one of which is studied in detail. The results are compared with those of two earlier analyses.
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    Bulletin of mathematical biology 43 (1981), S. 389-400 
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    Notes: Abstract A numerical study of the coupled nerve fibre problem is given which verifies and extends the perturbation theory of Luzader. Pulses on adjacent fibres can couple together with two possible stable pulse separations.
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    Bulletin of mathematical biology 43 (1981), S. 401-413 
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    Notes: Abstract A possible mechanism for effects of microwave radiation on the auditory system is the generation of field-induced forces at interfaces that divide materials of dissimilar electrical properties. A general expression for these “Maxwell stresses” is derived and then used to calculate the approximate magnitude of field-induced force within the organ of Corti during microwave exposure. Comparison of the results with data on the force needed to excite cochlear hair cells indicates auditory responses could be evoked by this mechanism at power densities near the threshold of rf hearing sensations.
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    Bulletin of mathematical biology 43 (1981), S. 415-426 
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    Notes: Abstract A definition of homogeneity for neural networks is given which permits their construction as group quotients. The significance of this for neural dynamics is discussed.
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    Bulletin of mathematical biology 43 (1981), S. 447-461 
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    Notes: Abstract The left ventricle is represented as a cylinder contracting both radially and longitudinally. A simple method is indicated to derive an expression for the rate of change of the kinetic energy of this three-dimensional model, which quantity can be used as an index for the study of the contractile behaviour of the myocardium. An application to the study of muscle mechanics is also indicated.
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    Bulletin of mathematical biology 43 (1981), S. 463-485 
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    Notes: Abstract A perturbation method is proposed to calculate approximately the limit cycle type nonequilibrium steady-state resulting from periodic perturbation of coefficients of stable population systems; the two species Lotka-Volterra competition system is explicity studied and the results are formulated for general multi-species population systems. Avoidance of competitive or other types of exclusion of species in a periodic environment is indicated.
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    Bulletin of mathematical biology 43 (1981), S. 513-516 
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    Bulletin of mathematical biology 30 (1968), S. 1-1 
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    Bulletin of mathematical biology 30 (1968), S. 27-32 
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    Notes: Abstract In a previous paper (Bull. Math. Biophysics,29, 565–574, 1967) the author developed equations to represent velocity and hematocrit profiles in quasi-Poiseuille flow of blood. It was assumed that energy dissipation was minimized and that the viscosity depended on hematocrit and shear rate according to the Casson formula. These equations are simplified considerably, placed in a form more suitable for numerical solution and shown to depend on a single dimensionless parameter. Typicalin vivo values for this parameter are calculated.
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    Bulletin of mathematical biology 30 (1968), S. 33-46 
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    Notes: Abstract In this paper, discrete models of reproduction are studied. In part one, definitions are given, particularly on order of the reproduction; part two concerns the growth of the population; part three, the phenomena of delay or acceleration; and part four, the consequences of mortality.
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    Bulletin of mathematical biology 30 (1968), S. 3-26 
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    Notes: Abstract A model of the regulation of thyroid hormone in the bloodstream of living systems is formulated and analyzed. The portion of this model defined as theregulator includes components representing the thyroid, anterior pituitary and hypothalamic organs and their intercommunicating channels, that is, the peripheral plasma and hypophysial portal circulations and certain neuro-secretory connections. The loss of hormones from the plasma in the living system associated with physiological mechanisms within the peripheral tissue space and the excretory pathways is represented in the model by a lumpedload on the regulator. The model is reduced to a system of differential equations involving eleven parameters and variables, all of which are identified with certain physiological structures and states. Five of these are currently observable by available laboratory techniques and two others are computable explicity from the equations of the model; the remaining four can be computed in the same way to within a multiplicative constant. Procedires for carrying out ten of these measurements and calculations are suggested. On the basis of the equations and parameters of the model, a discussion of the normal behavior and the response of this system to certain types of disturbances is presented. A systematic effort has been made in the development of this model to include all relevant physiological data and relationships reported in the biological literature. A summary of this literature, reflecting the views and interpretations made by the authors of this paper, is included for completeness and ease of reference.
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    Bulletin of mathematical biology 30 (1968), S. 47-59 
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    Notes: Abstract In this paper an expression is derived which describes the transient overall uptake of an inert solute by a section of tissue excised with parallel faces and placed upon an impermeable base. The approach diverges from the conventional analyses for perfused tissue (Morales and Smith,Bull. Math. Biophysics,6, 125–141, 1944;7, 47–99, 1945) because the extravascular zone is regarded as a heterogeneous diffusion medium. Account for this is taken by regarding tissue as effectively composed of two phases—a continuous (extracellular) phase similar to water, and a dispersed phase comprising cells of irregular profile. In both phases the relevant mode of uptake is taken as bulk diffusion rather than surface permeation, thus emphasizing the influence of the internal geometry of the tissue upon its overall exchange response.
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    Bulletin of mathematical biology 30 (1968), S. 87-104 
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    Notes: Abstract A method for the identification of flow systems by frequency domain analysis has been extended to include systems with recirculation and truncated data curves. Application of the technique to clinical indicator-dilution curves indicates that the method may be useful in the quantitation of intracardiac shunts. A number of numerical examples which demonstrate the accuracy of the method are included.
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    Bulletin of mathematical biology 30 (1968), S. 61-86 
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    Notes: Abstract By assigning time-varying coordinates to all environmental stimuli, it has been possible to axiomatize psychoanalytic theory on the five principles of multiple causation, growth-aging influence, genetic influence, historic influence and conscious-unconscious activity. The theorems of summation of response and the inevitability of conscious-unconscious conflict with their corollaries follow directly from the axiomatic foundations, as does the existence of an adaptation-defense mechanism. The interpretation of the defense mechanism in terms of an ego-id feedback system provides the basis for the structural existence of conscious-conscious and unconscious-unconscious conflict.
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    Bulletin of mathematical biology 30 (1968), S. 117-122 
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    Notes: Abstract In previous studies of (M,R) (Rosen, 1961; Demetrius, 1966), it was assumed that changes in the structure of (M,R) which were induced by environmental alternations occurred without error. Here, the effect of both “genetic” and “metabolic” malfunctions on the behavior of (M,R) is examined and a subclass of these systems whose behavior is invulnerable to such errors is specified.
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    Bulletin of mathematical biology 30 (1968), S. 105-116 
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    Notes: Abstract The definition of an (M,R) is formulated in a way that emphasizes its mathematical properties. Neglecting interactions between the components, it is shown that: (1) An (M,R) contains only one non-reestablishable component. (2) If an (M,R) contains only one non-reestablishable component, then that component is central. Examples are given to illustrate the biological significance of these two results. The notion of “lag-independence” is introduced, and it is shown that if a system possesses only one non-reestablishable component which is “lag-independent” then all components are lag-independent. The concepts of reestablishability, centrality and lag-independence are applied in order to suggest various criteria for optimal organization of (M,R).
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    Bulletin of mathematical biology 30 (1968), S. 123-133 
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    Notes: Abstract A mathematical representation for the analysis of control mechanisms in biochemical reactions is presented. First, the theoretical concept of concentration in biological systems is developed. Then a system consisting of two functions λ and τ is constructed as a network of single output automata. The range of λ is taken to be formed by a set of twostates qualitatively different from the “repair function” Φ f of a mappingf: A→B in the stimulated Φ1 and unstimulated state Φ0. Likewise, the range of τ is formed by the set δ={f o ,f 1} wheref 1 means the mappingf in its stimulated state andf o in the unstimulated one. It is demonstrated that the mathematical structure described acts as a control mechanism over thef and Φ f , so that two biochemical components,A→B, are transformed at a controlled rate. Some of the biological applications of this model are briefly examined. The Jacob-Monod model, the enzymatic adaptation phenomenon, and the “rheon unit” hypothesis are discussed within our framework. Eventually, a concrete model for the RNA-polymerase mechanism, based on the above discussion, is presented.
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    Bulletin of mathematical biology 30 (1968), S. 135-151 
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    Notes: Abstract The application of Rashevsky’s transformationT to a primordial graph yields a set of graphs corresponding to different stages in the development of the organism. However, sinceT is multiple-valued the graphs obtained are not ordered. To obtain an ordering, it is first shown that the set of graphs under consideration is equivalent to a well defined setO (for “organism”) ofn-tuples. A metric is then introduced which is based on a biological consideration discussed by Rashevsky (Bull. Math. Biophysics,16, 317–348, 1954). Since a metric implies an ordering of the setO, with a knowledge of the structure of the primordial, one can obtain the developmental sequence. Unfortunately, at present, the structure of the primordial graph is unknown which makes the direct application of the above principle impossible. Consequently, an indirect approach which makes use of more accessible biological phenomena is discussed as well. The hypothesis thatrate of development decreases exponentially and the implications this has with regard to the metric onO are discussed. It is shown that if the hypothesis is accepted the search for the developmental sequence is narrowed.
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    Bulletin of mathematical biology 28 (1966), S. 1-10 
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    Notes: Résumé Les premiers étages sensoriels sont étudiés en utilisant notre modèle de neurone et en supposant que les réseaux responsables de la perception sont particulièrement solides, stables, économiques. Nous montrons que les premiers neurones doivent être spontanément périodiques et autorégulés. La nécessité fonctionnelle des premiers étages de la voie visuelle est démontrée. Par analogie, nous étudions la voie auditive.
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    Bulletin of mathematical biology 28 (1966), S. 11-24 
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    Notes: Abstract The problem of the viscous flow of an incompressible Newtonian liquid in a converging tapered tube has been solved in spherical polar coordinates. The method of the solution involves the Stokes' stream function and a technique introduced by Stokes in the study of a sphere oscillating in a fluid. The theory for the flow in a rigid tube includes: (1) the pulsatile flow with both radial and angular velocity components; (2) the steady state flow with both radial and angular velocity components and (3) the very slow steady state flow with only a radial velocity component present. For a tapered elastic tube, the velocity of the propagated pulse wave is determined. The solution given is in terms of the elastic constants of the system and the coordinates for this type of geometry. The pulse velocity is then related to the velocity in an elastic cylindrical tube with the necessary correction terms to account for the tapered tube.
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    Bulletin of mathematical biology 28 (1966), S. 25-50 
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    Notes: Abstract In this paper a class of branching processes applicable to populations reproducing by some asexual means or by a simple selfing system of mating is studied. The paper is divided into three parts. In part one the mathematical model is introduced, part two is a mathematical analysis of the model, and in part three concrete applications and examples are given. Many of the proofs of the theorems in part two are omitted but will appear in a subsequent issue of theBulletin.
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    Bulletin of mathematical biology 28 (1966), S. 51-74 
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    Notes: Abstract The application of the earlier results (Pavlidis, T. 1965. “A New Model for Simple Neural Nets and its Application in the Design of a Neural Oscillator.”Bull. Math. Biophysics,27, No. 2, 215–229) to the design of more complex neural nets is attempted. The following cases are considered: 1. Chains of neurons where it is proven that the frequency of the output pulses does not depend on the value of the input as long as it is above a certain threshold. 2. Groups of neurons with backward inhibition which present an intermittent mode of operation. 3. Neural nets with periodic facilitation which permit time sharing of certain components for different functions. 4. A neural net which can detect the sign of the input even if the main receptor is sensitive only to the absolute value of it, is presented. 5. A velocity estimating neural net which in combination with one of the nets with intermittent response provides a model for the smooth eye tracking movements.
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    Bulletin of mathematical biology 28 (1966), S. 75-90 
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    Notes: Abstract By assigning coordinates to the information space comprising all knowledge, rigorous mathematical interpretations can be placed on such terms as academic ability, memory and creativity such that these psychometric concepts can be incorporated into a framework of functional analysis which then permits the optimization of long-term academic learning processes through the location of the teaching trajectories in information space which will maximize the knowledge accumulated in a generalized educational system composed of a complex of subject-pupil-teacher interactions. The concepts of discrete and continuous information spaces are discussed in connection with subject-subject, subjectpupil and pupil-pupil interactions, and the advantages of using variational versus dynamic programming methods of optimizing alternative educational systems are evaluated.
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    Bulletin of mathematical biology 28 (1966), S. 103-106 
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    Notes: Abstract IfK is a partition of a setK which is partially ordered by the relationR andR is a collection of pairs of sets ofK such that the sets of each pair are related byR in the sense of Rashevsky, thenR is a relation which partially ordersK. Necessary and sufficient conditions thatK be a chain are obtained, and ifK is a chain under these conditions, it is shown thatK is unique.
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    Bulletin of mathematical biology 28 (1966), S. 161-166 
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    Notes: Abstract This paper continues a comparison of the Taylor series and spherical harmonic forms of multipole representations initiated by Yeh (Bull. Math. Biophysics,24, 197–207, 1962). It is shown that while transformations from Taylor series form into spherical harmonic form is always possible, the inverse cannot be accomplished as suggested by Yeh; corrected transformation equations are given. It is also shown that direct measurement of Taylor coefficients, as outlined in Yeh, Martinek, and de Beaumont (Bull. Math. Biophysics,20, 203–216, 1958), is actually not possible. Accordingly, only the spherical harmonic coefficients can be determined by measurement of surface potentials, as in electrocardiography.
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    Bulletin of mathematical biology 28 (1966), S. 181-190 
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    Notes: Abstract This paper is a continuation of a paper, “Some Multi-Dimensional Branching Processes as Motivated by a Class of Problems in Mathematical Genetics I,” by C. J. Mode, which appeared in a previous issue of theBulletin. Its purpose is two-fold; namely to discuss the mathematical existence of the model and to supply the mathematical proofs of some theorems in section two of the paper mentioned above. This paper should be read in conjunction with the previous paper.
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    Bulletin of mathematical biology 28 (1966), S. 191-194 
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    Notes: Abstract Rosen (Bull. Math Biophysics. 1959) has argued that a self-reproducing automaton of the type originally described by von Neumann is impossible because of a logical paradox inherent in its definition. The paradox is resolved by explicitly allowing errors (mutations) in the system and thus introducing evolution. There is no paradox in an automaton, originating from a slightly different ancestor through mutation. The von Neumann model thus becomes realistic and useful for a discussion of biological phenomena.
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    Bulletin of mathematical biology 28 (1966), S. 167-179 
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    Notes: Abstract Previously proposed formulae for the quantitative estimation of bidirectional shunts across ventricular septal defects require determination of the oxygen contents of mixed venous, pulmonary artery, pulmonary venous, and aortic blood. Because these formulae do not take into account the mixing of oxygenated with unoxygenated blood within the ventricles, their use must result in underestimation of shunt flows in each direction. A mathematical model for a ventricular defect is examined, in which it is assumed that mixing of blood occurs in each of six sites in the venae cavae or right atrium, right ventricle, pulmonary artery, left atrium, left ventricle, and aorta. A total of fourteen streams of blood can flow from one to another of these mixing sites. As long as complete mixing occurs in the six specified mixing sites, any degree of mixing or non-mixing of the various streams is permitted. From the equations characterizing the model, formulae are derived in which the shunt flow in each direction is expressed in terms of the oxygen contents in the six mixing sites and the fractions of blood which enter the shunt from either side without prior mixing in a ventricular mixing site. The previously reported formulae, which apply when no ventricular mixing is allowed to occur, lead to theoretical minimum values for the shunt flows in each direction. At the opposite extreme where all the shunting blood is required to mix in a ventricle before entering the shunt, formulae for maximum possible shunt flows are also obtained. The absolute values for the left-to-right and right-to-left shunt flows, which must lie somewhere between the theoretical maximum and minimum values, cannot be computed from blood gas data alone.
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    Bulletin of mathematical biology 28 (1966), S. 195-205 
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    Notes: Abstract Experimental evidence strongly suggests that the contractility of the intact heart in situ, in contrast to that of striated muscle elsewhere in the body, is controlled in a close-cycle system. Thus, the variation of intraventricular pressure during systole follows a complex pattern, whose relative form remains quite constant regardless of the duration of ejection. By use of the single-chambered model of the cardiovascular system, a mathematical representation of a feasible feedback mechanism is developed. The requirement that the feedback system must satisfy mathematical principles eliminates relationships apparently reasonable from a physiological viewpoint. A clinical application which the mathematical development suggests is that early arterial hypertension may arise from an abnormal feedback mechanism with excessively large cardiac output in the initial portion of systole.
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    Bulletin of mathematical biology 28 (1966), S. 207-216 
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    Notes: Abstract Due to the lack of direct X-ray evidence for base pairing being the only mechanism for the formation of double helix in a DNA crystal, an alternative explanation is suggested so that the observed DNA loop becomes essential.
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    Bulletin of mathematical biology 28 (1966), S. 219-233 
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    Bulletin of mathematical biology 28 (1966), S. 217-218 
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    Notes: Abstract Validity of group ring expression of selfed population is shown for cases in which there are differences in recombination probabilities between two sexual sides of a plant.
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    Bulletin of mathematical biology 28 (1966), S. 261-282 
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    Notes: Abstract An integral equation analysis of generaln compartment steady state systems imbedded in static media of arbitrary complexity has been developed. A set of initial entry functions can be found which serve to determine a corresponding set of partitioned initial entry functions. The partitioned functions, in turn, can be used to predict the probabilities and time courses of various transport histories and to determine all steady state rates of flow between measured compartments. The method is quite general, being completely applicable, for example, to closed systems, to cyclic systems and to systems in which relatively rapid (but finite) exchange between compartments occurs.
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    Bulletin of mathematical biology 28 (1966), S. 309-313 
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    Notes: Abstract From the definition of a strong and weakn-ary relation betweenn sets, given in a previous paper (Bulletin of Mathematical Biophysics,27, 477–492), it follows that for a given set ofn sets and givenn-ary relationR between them there can exist only one strong relation, but a large number of weak ones. An expression for the total number of possible weak relations is derived and the notion of the degree of weakness of a relation is introduced and discussed.
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    Notes: Abstract The problem of determining the sequence of a biopolymer from its fragments is stated in mathematical terms. Using concrete properties of a free monoid, certain general classes of biopolymers are shown to be insolvable from fragment data produced by complete digestion where enzymes specific for any possible combination of chemical bonds are employed.
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    Bulletin of mathematical biology 28 (1966), S. 283-308 
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    Notes: Abstract To the extent that all biological phenomena are perceivable only through their physical manifestations, it may be justified to assume that all biological phenomena will be eventually represented in terms of physics; perhaps not of present day physics, but of some “extended” form of it. However, even if this should be correct, it must be kept in mind that representing individual biological phenomena in terms of physics is not the same as deducing from known physical laws the necessity of biological phenomena. Drawing an analogy from pure mathematics, it is possible that while every biological phenomenon may be represented in terms of physics, yet biological statements represent a class of “undecidable” statements within the framework of physics. Such a conjecture is reinforced by the history of physics itself and illustrated on several examples. The 19th century physicists tried in vain todeduce electromagnetic phenomena from mechanical ones. A similar situation may exist in regard to biological and social sciences. Quite generally, the possibility of representing a class B phenomena in terms of class A phenomena does not imply that the phenomena of class B can be deduced from those of class A. The consequences of the above on the relation between physics, biology, and sociology are studied. A tentative postulational formulation of basic biological principles are given and some consequences are discussed. It is pointed out that not only can the study of biological phenomena throw light on some physical phenomena, but that the study of social phenomena may be of value for the understanding of the structures and functions of living organisms. The possibility of a sort of “socionics” is indicated.
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    Bulletin of mathematical biology 28 (1966), S. 371-374 
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    Notes: Abstract It is shown that any (ℳ ℛ) has some component which cannot be re-established after it has been inhibited. If there is only one such component, it must be central, that is, its inhibition stops the whole system. These results hold even when it is not assumed that ℳ is connected.
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    Bulletin of mathematical biology 28 (1966), S. 315-331 
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    Notes: Abstract In this paper a theory of a class of restricted transition probabilities is developed and applied to a problem in the dynamics of biological populations under the assumption that the underlying stochastic process is a continuous time parameter Markov chain with stationary transition probabilities. The paper is divided into three parts. Part one contains sufficient background from the theory of Markov processes to define restricted transition probabilities in a rigorous manner. In addition, some basic concepts in the theory of stochastic processes are interpreted from the biological point of view. Part two is concerned with the problem of finding representations for restricted transition probabilities. Finally, in part three the theory of restricted transition probabilities is applied to the problem of finding and analyzing some properties of the distribution function of the maximum size attained by the population in a finite time interval for a rather wide class of Markov processes. Some other applications of restricted transition probabilities to other problems in the dynamics of biological populations are also suggested. These applications will be discussed more fully in a companion paper.
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    Bulletin of mathematical biology 28 (1966), S. 433-441 
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    Notes: Abstract Equilibrium solubility considerations are presented based on the assumption that equating the kinetic expressionq, developed in part I, to zero can describe the equilibrium or steady state between hydroxyapatite and salt solutions. From this expression is derived Hodge's empirical equilibrium equation,C=KH. Further, a lograithmic transformation of this equation results in an expression that accounts for the equilibrium calcium, phosphorus andpH relation found by Levinskas and Neuman. Finally, it also shows the relation between log (C·P) andpH necessary for typical artificial carious lesions as found by Coolidge, Besic and Jacobs. A discussion of a recent theory of hydroxyapatite solubility of LaMer reveals calculation errors that vitiate his results. It is shown that logK 1 (K 1 is the ratio of the rate constants inq and can serve as a solubility equilibrium constant for hydroxyapatite) varies by only 1.2 units when calculated from three diverse sets of data. This variation is less than that reported by LaMer (when the errors of calculation in that work are corrected) and considerably less than the range of 11 among attempts to calculate a conventionalpK sp , as summarized by Hodge.
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    Bulletin of mathematical biology 28 (1966), S. 465-475 
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    Notes: Abstract In imitative behavior, as studied previously by N. Rashevsky (Mathematical Biology of Sociol Behavior, Chapter XIII, The University of Chicago Press, 1950), the reason for the majority of a society to accept a particular behavior is based on purely voluntary action (band-wagon effect). In the present paper effects of coercion of the majority by a small minority group which poses the means for coercion, are studied. More general types of equations are thus obtained and threshold effects found, which bear a resemblance to some such effects studied previously.
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    Notes: Abstract Part III attempts to develop a diffusion controlled model of caries in the intact enamel employing the kinetic results of the previous two parts. A model of the enamel as a granular bed with a diffusible organic matrix filling the interstices is considered. The basic equations of diffusion and simultaneous reaction are developed under the assumption that all the reactions are so rapid as compared with the diffusion rate, that they are in a quasi-equilibrium state. The resultant system of seven coupled, non-linear parabolic partial differential equations is of such complexity that only numerical solutions could be attempted. Stability restrictions inherent in the problem dictated the use of the DuFort-Frankel numerical solution for parabolic boundary problems. Numerical solutions giving the concentration of all reactants, the rate of mineral loss, and the enamel porosity were obtained for a variety of boundary conditions. It is found that departure from the equilibrium condition expressed in part II is necessary for the occurrence of an attack on the enamel. The rate and pattern of penetration is then determined primarily by the concentrations of undissociated buffer, and salts, together with the rate of diffusion in the surrounding medium. The possibility of a relatively intact surface layer persisting over a demineralized subsurface region due solely to the composition of the demineralizing medium is noted. Remineralization behavior in portions of the carious lesion occurs in the model under certain boundary conditions.
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    Bulletin of mathematical biology 43 (1981), S. 59-67 
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    Notes: Abstract The theory of computational complexity and certain explicitly-stated hypotheses imply limitations on the information processing power of biological systems. Parallelism, special purpose organization, and analog mechanisms may provide speedup critical for life processes, but have little power in the face of exponential growth. We show that “polynomially simulatable” biological systems cannot exhibit dynamic behavior which produces the solution of an intractable problem. The argument implies that parallelism does not allow biological systems to defeat the exponential explosion, but rather is important because it allows polynomial time algorithms to be used more efficiently.
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    Bulletin of mathematical biology 43 (1981), S. 81-88 
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    Notes: Abstract A correlation matrix analysis is applied to the base sequence of MS2 and ϕX174 in comparison with sets of simulated sequences with different degrees of constaint Significant differences between a codified sequence, and a statistical one in terms of the “correlation matrix” for sets of different length cannot be found. This result is analysed in terms of nucleotide sequences with different levels of informational content.
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    Bulletin of mathematical biology 43 (1981), S. 101-109 
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    Notes: Abstract A method of calculating the volume of a tree distal to a cut at the origin of a branch, using branching, diameter and length ratios, has been developed. The method was applied to bronchial tree casts from human, dog, sheep, hamster, and rat lungs. It was found that the exponenta in the equation weight=k×diameter a is approximately equal to 3.0 in sheep lung casts, as found by Hooper (1977), but it is greater than 3.0 in casts from the other four species.
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    Bulletin of mathematical biology 43 (1981), S. 111-116 
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    Notes: Abstract In this note we examine a continuous time version of a compartmental model introduced in a discrete time setting by S. R. Bernard. The model allows for more than one particle to leave the system at any time. This introduces additional randomness into the system, over the pure death system and this is reflected in the variance function.
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    Bulletin of mathematical biology 43 (1981), S. 89-99 
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    Notes: Abstract The mean first passage time for free diffusion can be derived directly by solving a simple analogue steady state problem. In this problem the diffusion starting region is considered as a time independent source of diffusing particles and the diffusion target assumes the behaviour of a perfectly absorbing sink. It is shown here that the transit time between the source and the sink, which in this particular problem is equal to the ratio between the holdup of the system and the total flux, is identical to the Brownian movement concept of the mean first passage time for free diffusion. This established identity considerably facilitates the derivation and investigation of the timing of diffusion in complicated structures such as those commonly found in living organisms.
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    Bulletin of mathematical biology 43 (1981), S. 121-123 
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    Bulletin of mathematical biology 43 (1981), S. 117-120 
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    Bulletin of mathematical biology 43 (1981), S. 201-211 
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    Notes: Abstract In this paper three stochastic models are developed for a class of two-compartment systems to analyse the randomness of the leaving process of the particles in the system. Results in closed form for the distribution of the leaving process of the particles in the system are given both for general and exponential sojourn time distributions and also in association with forward recurrence time distributions with and without Poisson input.
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    Bulletin of mathematical biology 43 (1981), S. 213-232 
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    Notes: Abstract Two simple models are proposed and analysed, in which it is shown that the formation of a new polymer, resulting from an “error” in the template action mechanism of production of an old polymer, may compromise the stability of the initial system under specific conditions, in the context of prebiotic evolution. Autocatalysis is shown to be a “selective advantage”, enabling the “mutant” to dominate in concentration and even replace the initial polymer. The addition of a third molecule playing the role of a catalyst causes hysteresis effects.
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    Bulletin of mathematical biology 43 (1981), S. 165-181 
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    Notes: Abstract The problem of extinction of the prey population in a microbial predator-prey interaction in a chemostat has been examined. Usual deterministic lumped parameter models were used for the dynamics of the chemostat for large numbers of the two populations; the generalized birth and death stochastic process was employed for the description of the random variations at small prey numbers. Extinction probabilities of the prey population were calculated for different holding times and chemostat volumes, and their dependence upon the growth parameters of the two populations was studied. It was found that extinction was possible when the Monod model was used for the specific growth rate of the predators as a function of the prey number density. On the other hand, the decrease of the feeding activity of the predators at low prey densities predicted by the multiple saturation model acts as a regulatory factor that prevents extinction of the prey. In view of the fact that extinction of the prey has never been observed in the laboratory, the latter model seems more appropriate to describe the dynamics of microbial predation.
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    Bulletin of mathematical biology 43 (1981), S. 233-238 
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    Notes: Abstract During exposures of the eye to light, the choroidal circulation may have a regulatory influence on the retinal temperature. This is investigated using a mathematical model and a finite-difference technique. It is predicted that the choroidal blood flow a small effect on retinal temperature, which may be important.
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    Bulletin of mathematical biology 43 (1981), S. 427-446 
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    Notes: Abstract A probabilistic model of a spatially localized, mutually exitatory (inhibitory) population of neurons is formulated to help explain average evoked potential and post-stimulus time histogram measurements. The model is based on the stochastic activity of single neurons within interactive masses of neurons which exhibit co-operative behavior. Macrostate variables corresponding to the above measurements are related through the model to features of neural operation at the individual and ensemble level. Steady-state solution are obtained and their physiological implications are discussed.
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    Bulletin of mathematical biology 43 (1981), S. 503-512 
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    Notes: Abstract We consider a one-compartment system with stochastic transfer rate characterized either by Gaussian or by two-level jump process and study the time evolution of the (statistical) moments of the (random) amount of the substance present in the system. The effect of the coloured as well as of the white noise is investigated and it is found that the presence of stochasticity in the transfer rate parameter increases the relaxation time of the system. Finally, we obtain the conditions for the stability of the system in the moment sense.
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    Bulletin of mathematical biology 43 (1981), S. 487-501 
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    Notes: Abstract A model is described in which damage to a single intracellular locus can lead to a tumorigenic transformation. Assuming a large number of independent intracellular loci to be at risk and assuming that damage to a locus sufficient to cause a tumorigenic transformation occurs with probability greater than zero for all doses greater than zero, leads to the use of the Weibull distribution to characterize the probability of a nonspontaneous tumorigenic cellular transformation occurring after exposure to a given dose of carcinogen. The excess lifetime tumor incidence (i.e., the proportion of tumor bearers) above the spontaneous incidence is used as an estimate of the non-spontaneous incidence and is characterized by a tumor incidence function that represents the probability of occurrence of one or more non-spontaneous tumorigenic cellular transformations amongN(D) independent surviving cells per individual, after exposure to a doseD of carcinogen. The tumor incidence function is fitted to published data for the excess tumor incidence after exposure of animals or humans to ionizing radiation and after exposure of animals to chemical carcinogens.
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    Bulletin of mathematical biology 43 (1981), S. 549-561 
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    Notes: Abstract This paper deals with a stochasticn-compartment irreversible system with a non-homogeneous Poisson input and arbitrary residence time for each of the compartments. Results relating to the number of particles present in each of the compartments as well as the total number of particles present in the system at any time are derived. Further, explicit expressions for the auto covariance function for each compartment and the cross-covariance function between any two compartments with a given time lag are obtained. As a particular case, then-compartment irreversible system is analyzed with homogeneous Poisson input and exponential residence time distribution for each of the compartments. The possible applications of the model are discussed.
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    Bulletin of mathematical biology 43 (1981), S. 563-577 
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    Notes: Abstract This paper deals with the pulsatile blood flow in the lung alveolar sheets by idealizing each of them as a channel covered by porous media. As the blood flow in the lung is of low Reynolds number, a creeping flow is assumed in the channel. The analytical and numerical results for the velocity and pressure distribution in the porous medium are presented. The effect of an imposed slip condition is also studied. Comparisons with the corresponding results for the steady-state case are made at the end.
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    Bulletin of mathematical biology 43 (1981), S. 579-591 
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    Notes: Abstract The relationships that define the structure of a given ecosystem, social system, or even a physiological function can only exist if certain parameters are confined to a certain range of values. As the values change and exceed this given range the relationships are forced to change, and so produce a new pattern of relationships. The concept of a dynamic structure captures this potential for structural change in relation to a set of parameters. The precise definition of structure and allowable transformation constitutes the definition of a category. The total range of parameters associated with all the relevant structures provides a parameter space which is assumed to be a manifold. Maps with extra structure from the manifold to the category define dynamic structures. The domain of differential dynamic systems is the manifold, and a flow or movement across the manifold is associated with a series of structural transformations in the category. In some cases a structure outruns its parameter range, to be faced with an obstruction—an absence of possible transformations. Ways of studying such “obstructions” are considered along with the related problem of extending a dynamic structure beyond a previously given set of parameters. The cost or resistance of transformations is also studied. The concepts of dynamic structures are illustrated by the structural change of food webs and they are used in a necessarily qualitative fashion to study dominance structures of social orders and finally to speculate on the qualitative nature of evolutionary change of functional aspects of organisms.
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    Bulletin of mathematical biology 43 (1981), S. 705-715 
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    Notes: Abstract The preceding paper (Thorn, 1981) has shown that in a linear pharmacokinetic system with a multimodal impulse response the peak drug level may sometimes be smaller with slower rates of injection. This paper presents two theorems on this paradoxical injection rate effect where the injection is a constant infusion of finite duration. The first theorem establishes a graphical method for determining whether a given impulse response will give a paradoxical injection rate effect; and the second establishes that the maximum paradoxical increase in peak drug level is by a factor of two. It is further shown that in order to approach this maximum paradoxical increase the impulse response must contain two isolated, sharp, narrow pulses of approximately equal area. Some examples of bimodal arterial dye-dilution curves from the literature are discussed as impulse responses; and there is also a discussion of the behavior of drug level maxima and minima at different injection rates.
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    Bulletin of mathematical biology 43 (1981), S. 693-703 
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    Notes: Abstract This paper presents three theorems on the peak drug levels that result from injection into a linear pharmacokinetic system. As a preliminary, the “rate of injection” is defined in terms of time expansion or time contraction of the injection function (input). The first theorem then states that the peak drug level will not be greater when the rate of injection is slow than when it is fast, if the impulse response is unimodal. The second theorem sets limits for the time of the maximum drug level, in relation to the time of the maximum of the (unimodal) impulse response and the duration of the input. The third theorem defines conditions which assure a definitely lower peak drug level if the rate of injection is slower. A graphical method is suggested for determining the times and magnitudes of the peak drug levels that result from constant infusions of a fixed dose at different rates. An example is provided to show that if the impulse response is multimodal then the peak drug level may sometimes increase with a decrease in the injection rate.
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    Bulletin of mathematical biology 28 (1966), S. 91-102 
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    Notes: Abstract In previous papers (1955–1957) a theory of biological similarity was established, assuming that the limits are the mechanical and the electrodynamical similarity criteria. The range of this theory lies between the coefficient of the time exponent (γ) for mechanical (0.5γ) and electrodynamical (1.0γ) similarities, being the mode 0.93γ. Moreover, for certain functions this restricted theoretical range should be extended to the hydrodynamical similarity criterion (2γ), so that the dimensionless numbers commonly used in Physics (Reynolds, Froude, Weber, etc.) can be included within the total range (0.5–2γ) of biological similarities. From dimensional analysis of physiological, functions it was possible to obtain, by means of dimensional and solution matrices, a group of “nondimensional numbers” by applying Buckingham's Pi-theorem. Nevertheless, only if a single similarity criterion was applied, the residual weight exponent was exactly zero; in all other instances the weight exponent was not zero, due to the existence of a range for biological similarities and to the statistical meaning of exponent (b) of the allometric equations. From the similarity criteria “invariant numbers” can be obtained, by means of which it is possible to establish correlations between numerous morphological and physiological characteristics of a particular system (circulation, respiration, metabolism, etc.).
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    Bulletin of mathematical biology 28 (1966), S. 117-124 
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    Notes: Abstract The notion of relations between sets, defined in a previous publication (Bull. Math. Biophysics,23, 233–235, 1961) is generalized and some biological examples are given. A generalization ton-ary relation is suggested.
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    Bulletin of mathematical biology 28 (1966), S. 107-116 
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    Notes: Abstract A method is introduced for using matrices to represent the organism-graphs of Rashevsky's theory of biotopological mapping. The representation is made in such a way as to reveal the structure of these graphs. Using insight gained from the consideration of the matrix representations, a theorem is proved concerning the primordial origins of organisms and counterexamples are displayed to show the necessity of the hypotheses of this theorem.
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    Bulletin of mathematical biology 28 (1966), S. 137-138 
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