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  • 1
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    Bulletin of mathematical biology 41 (1979), S. 893-898 
    ISSN: 1522-9602
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract Biological tree-like structures, such as mammalian tracheobronchial airways, are complicated branching systems. One problem in modeling such systems is the reassignment of the number of segments at a given generation in the model being constructed. A hypothesis is proposed which has successfully been used in modeling mammalian lung airways.
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  • 2
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    Bulletin of mathematical biology 37 (1975), S. 37-49 
    ISSN: 1522-9602
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    Notes: Abstract The chromosomal theory of inbreeding based on a gametic interaction system lead us to define a depression coefficientD. Comparison of random, sib and half-sib matings (with inbreeding coefficientF=0, 1/4 and 1/8) shows thatD depends on the structure of the starting population and on values of the model parameters. This result accounts for responses of lines whose depression does not depend directly on the inbreeding coefficient and which theories of inbreeding based on increasing homozygosity fail to explain.
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  • 3
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    Bulletin of mathematical biology 37 (1975), S. 59-69 
    ISSN: 1522-9602
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    Notes: Abstract An idealization of chemical combination is formulated as a model of computability, and it is shown that this model has universal computational power just in case assembly has at least two-dimensional space in which to occur. It is also shown that this model, under reinterpretation, corresponds to a cellular automaton in which growth occurs by differentiation only (i.e., the state into which any cell is born is thereadfter fixed). Hence this latter model of growth is also computationally universal.
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  • 4
    ISSN: 1522-9602
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    Notes: Abstract Kinetics of biological light emission processes do not mean what they seem to mean, because measured light intensity is not proportional to reactant concentration but to reaction rate. Therefore, the differential equation for light decay is usually different from that of concentration decay, so that mass action interpretations cannot be applied directly to light intensity decay. An observed second order light decay for Chlorella at 6.5°C, implies Elovich solid state reaction kinetics, which agrees with other evidence for solid state processes in photosynthesis. An observed 1.5 order light decay for Cholorella at 28°C implies second order liquid or solid state reaction kinetics. First ordere light decay implies first order reaction kinetics.
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  • 5
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    Bulletin of mathematical biology 37 (1975), S. 71-78 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract Analysis based on the integration of differential inequalities is employed to derive upper and lower bounds on the total populationN(t) = ∫ R θ(x 1,x 2,t) dx 1 dx 2 of a biological species with an area-density distribution function θ=θ(x 1,x 2,t) (≥0) governed by a reaction-diffusion equation of the form ∂θ/∂t =D∇2θ +fθ −gθ n+1 whereD (〉0),n (〉0),f andg are constant parameters, θ=0 at all points on the boundary ∂R of an (arbitrary) two-dimensional regionR, and the initial distribution (θ(x 1,x 2, 0) is such thatN(0) is finite. Forg≥0 withR the entire two-dimensional Euclidean space, a lower bound onN(t) is obtained, showing in particular thatN(∞) is bounded below by a finite positive quantity forf≥0 andn〉1. An upper bound onN(t) is obtained for arbitrary bounded or unbounded)R withn=1,f andg negative, and ∫ R θ(x 1,x 2, 0)2 dx 1 dx 2 sufficiently small in magnitude, implying that the population goes to extinction with increasing values of the time,N(∞)=0. Forg≥0 andR of finite area, the analysis yields upper bounds onN(t), predicting eventual extinction of the population if eitherf≤0 or if the area ofR is less than a certain grouping of the parameters in cases for whichf is positive. These results are directly applicable to biological species with distributions satisfying the Fisher equation in two spatial dimensions and to species governed by certain specialized population models.
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  • 6
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    Bulletin of mathematical biology 37 (1975), S. 127-138 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract The equilibrium probability distribution of the process level is studied for a general class of reversible stochastic reactions. A calculationally convenient approximation for equilibrium probabilities is derived and its accuracy is investigated over a range of values of the equilibrium constant. A method of approximating the equilibrium means and variance is developed and illustrated forQ th-order processes.
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  • 7
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    Bulletin of mathematical biology 37 (1975), S. 565-572 
    ISSN: 1522-9602
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    Notes: Abstract Beside the concept of material inputs and outputs of components of the representation of biological systems given to us by Rosen, the concept of energy is incorporated. The interaction of material and energy is represented by a cartesian product; and separate material and energetical mappings are considered as the new representation of components. These developments generate aMα category, and it is shown thatMα is isomorphic to theM category of previous developments.
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    Bulletin of mathematical biology 37 (1975), S. 555-564 
    ISSN: 1522-9602
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    Notes: Abstract This paper discusses the solution of a generaln-compartment system with time dependent transition probabilities utilizing the technique described by Cardenas and Matis (1975) (hereafter abbreviated (CM)). In addition, the cumulant generating function is derived for a special class of reversiblen-compartment systems where the time-dependent intensity coefficients corresponding to the migration and death rates are some multiple of each other. The immigration rates can be any integrable function of time. The moments are also obtained and the solution to the two-compartment system is presented explicitly. The solution is illustrated with a linear and a periodic function which forms have been widely reported in the literature.
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  • 9
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    Bulletin of mathematical biology 37 (1975), S. 573-588 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract The relations (inflow) = (dose)/(area under indicator curve), and (volume of distribution) = (throughflow) × (mean transit time) are derived by a matrix method for a system of interconnected subsystems, within which spatial indicator activity gradients may exist, and for compartments, within which the indicator activity is spatially uniform. The inflow theorem, is different from the outflow theorem. Equivalent labeling of multi-input systems reduces them formally to single input systems. Foreign indicator flow-volume kinetics are more general than, and include as a special case, tracer flux-mass (metabolic) kinetics. Volume of distribution in the indicator steady state may be different from the equilibrium volume of distribution.
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    Bulletin of mathematical biology 37 (1975), S. 219-219 
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    Bulletin of mathematical biology 37 (1975), S. 291-299 
    ISSN: 1522-9602
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    Notes: Abstract Perturbation methods are applied to a differential equation predator-prey model to find the approximate amplitudes and period of limit cycle solutions. In the model the feeding rate per unit predator per unit prey decreases as the prey become scare. The rigorous applicability of the perturbation technique depends on the assumptions that the limit cycle amplitude is relatively small and that near the equilibrium point the growth rate of each species is most sensitive to changes in the density of the other species. The second assumption is usually roughly satisfied in practice and examples are considered which suggest that the first assumption can be greatly relaxed.
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    Bulletin of mathematical biology 37 (1975), S. 367-387 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract Signal Detection Theory can be used to provide a mathematical model describing the choice of a predator trying to distinguish between a model and a Batesian mimic. The mathematical model yields a number of a deductions, in particular that it may or may not assist the mimic population if mimics more closely resemble their models. The assumptions underlying the analysis are discussed in some detail.
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  • 13
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    Bulletin of mathematical biology 37 (1975), S. 419-425 
    ISSN: 1522-9602
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    Notes: Abstract A new type of physical transition, denotedS→S *, has been detected in irradiated organic molecules (λ=546 nm) through their interaction with specific biological macromolecules. In a specific enzyme-substrate interaction, a clear enhancement of the reaction rate is observed, when the substrate is irradiated with sharply well defined times. These “efficient irradiation times” are always of the 5k sec type (k=1, 2, 3, …). They have been consistently revealed in a great number of specific biological interactions. The present note demonstrates an important property, i.e. that forevery irradiation time aS→S * transition is induced in organic molecules. It is shown that for any irradiation times different from the 5k sec type (k=1, 2, 3, …) states of theS * type may occur, but the biological macromolecules may “detect” only theS * states induced by irradiations of the 5k sec type.
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    Bulletin of mathematical biology 37 (1975), S. 459-470 
    ISSN: 1522-9602
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    Notes: Abstract A semi-empirical model applicable to the flow of blood and other particulate suspensions through narrow tubes has been developed. It envisages a central core of blood surrounded by a wall layer of reduced hematocrit. With the help of this model the wall layer thickness and extent of plug flow may be calculated using pressure drop, flow rate and hematocrit reduction data. It has been found from the available data in the literature that for a given sample of blood the extent of plug flow increases with decreasing tube diameter. Also for a flow through a given tube it increases with hematocrit. The wall layer thickness is found to decrease with increase in blood hematocrit. A comparison between the results of rigid particulate suspensions and blood reveals that the thicker wall layer and smaller plug flow radius in the case of blood may be attributed to the deformability of the erythrocytes.
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    Bulletin of mathematical biology 37 (1975), S. 489-504 
    ISSN: 1522-9602
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    Notes: Abstract Three dimensional laminar, viscid flow is developed for Newtonian fluids which provides absolute values for axial, radial and tangential velocity fields everywhere if the dimensions of the vessel are known and two simultaneous axial velocities e.g. on and off the central axis in the same plane, and the central axis axial velocity gradient are measured. In addition, normal and shear stresses are determinable. The equation set satisfies geometric and other known flow limiting conditions such as no slip at surfaces etc. and are amenable for inclusion in general, dynamic flow expressions. Alternatively they may be used alone for certain problems involving gradients and secondary flows. A range of illustrations are shown for a distorting vessel with elliptic cross-section and small axial taper (analogous to the pulmonary trunk during ejection).
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    Bulletin of mathematical biology 37 (1975), S. 521-553 
    ISSN: 1522-9602
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    Notes: Abstract A regulated left ventricular dynamics model is presented which involves interaction of the dynamics of the left ventricular and circulatory systems and their regulation by the central nervous system. On-line human parametric simulation (parameter estimation) and consequential prognostic implications (based on parametric values) are demonstrated. Model responses to simulated physiologic stresses help delineate tolerances of subjects. In order to have an estimate of the reliability of the model, the sensitivity of the model's responses to changes in the values of its intrinsic parameters is assessed. Also determined is the extent to which errors in measuring the pressure affect the calculated values of the model's simulation parameters and subsequently influence the values of other diagnostically useful variables (such as contractility, oxygen consumption rate, heart rate), when the model is used to determine the limiting physiological stress sustainable by the subject. A comparison of the model's composition with those of other similar cardio-circulatory models is included.
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    Bulletin of mathematical biology 37 (1975), S. 659-673 
    ISSN: 1522-9602
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    Notes: Abstract Then-stage harvesting strategy of Elizarov and Svirezhev is examined. As a result, some important new features appear. A discussion is presented on whether or not one should harvest a species at one time stage or wait until a later time. The paper is concerned with contributions which are primarily mathematical formulations and results for continuous, as well as discrete time, logistic growth of a single species being harvested. Age class structure is ignored.
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    Bulletin of mathematical biology 40 (1978), S. 45-58 
    ISSN: 1522-9602
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    Notes: Abstract For certain environments, the Darwinian model allows unique prediction of a function that any surviving system adapted to such an environment has to perform. This is the case for those environments that determine a “survival functional” of position in space-time of known shape. Purely temporal survival functionals can be distinguished from spatial and mixed ones. In each case, there exists an optimum path in combined physical and (reduced) metabolic space. Dependent on the admissible error, approximate solutions of different complexity are sufficient. All solutions possess an afferent, a central, and an efferent part. Within this general frame, specific, “probably simplest”, solutions are proposed for adaptive chemotaxis, insect locomotion, lower vertebrates locomotion, higher vertebrates locomotion, chronobiological systems, and immune systems, respectively—or rather, for the underlying functionals.
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    Bulletin of mathematical biology 40 (1978), S. 59-77 
    ISSN: 1522-9602
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    Notes: Abstract Mathematical models afford a procedure of unifying concepts and hypotheses by expressing quantitative relationships between observables. The model presented indicates the roles of both insulin and glucagon as regulators of blood glucose, albeit in different ranges of the blood glucose concentrations. Insulin secretion is induced during hyperglycemia, while glucagon secretion results during hypoglycemia. These are demonstrated by simulations of a mathematical model conformed to data from the oral glucose tolerance test and the insulin infusion test in normal control subjects and stable and unstable diabetic patients. The model studies suggest the parameters could prove of value in quantifying the diabetic condition by indicating the degree of instability.
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    Bulletin of mathematical biology 40 (1978), S. 123-131 
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    Notes: Abstract A model for the dynamics of a single-species population whose birth rate depends on densities of previous generations is introduced. A difference equation formulation is proposed and the solutions classified for the various parameter values. Data from an experimental population of mice growing in limited space is cited and compared with the model predictions.
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    Bulletin of mathematical biology 40 (1978), S. 161-182 
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    Notes: Abstract All soft tissues are modeled as either one-dimensionalstrings, two-dimensionalmembranes, or three-dimensionalsolids. Attention is restricted to tissues in which one of the principal stress components is large and positive in comparison with the other negligible components. Results indicate the following: (1) If a deformed string isconstrained to lie on a surface and is free of tangential pressure, the tension is carried by rays which are geodesics of the surface. If a string or membrane isfree to deform in space without normal pressure, the tension rays are straight lines. If a membrane deforms without tangential surface loads, the tension rays are always geodesics on the deformed surface. If a solid deforms without body forces, the tension rays are straight lines. (2) The stress in a string is a constant if the string is free of tangential pressure and has constant cross-sectional area. The stress in flat tension fields free of tangential surface loads decays inversely with distance along a tension ray from the edge of regression. The stress in a spherically symmetric tension field free of body forces decays inversely with the square of the distance from the center of the sphere. (3) Stress singularities can occur in soft tissues, such as at the corners of a closed rectangular hole in a flat membrane strip. (4) The tension rays in the torsion of soft annular membranes are more steeply inclined from the radial direction than the tension rays for hard metals equally displaced.
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    Bulletin of mathematical biology 40 (1978), S. 211-221 
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    Notes: Abstract Non-steady-state equations for kidney models are stated. General conservation relations for these equations are derived. Transient equations for the central core model of the renal medulla are developed. Solution of the equations by Laplace transform methods for time invariant volume flows is discussed. The general theory of solving models with time dependent flows by finite difference methods is developed.
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    Bulletin of mathematical biology 40 (1978), S. 513-524 
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    Notes: Abstract The behavior of large systems of randomly-interacting variables is examined using an intentionally simplified model. The stable positive solutions are found to exhibit to a significant degree some well-known properties of ecological systems. This resemblance (including for example the predominance of “predator-prey” interactions) is all the more striking in view of the lack of biological “data” at the input end. The findings suggest it advisable to distinguish two kinds of properties in ecosystems. One kind would depend on specifically biological mechanisms; the other would characterize a wide class of persistent systems, and arise from the need for a dynamic balance between positive and negative feedback.
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    Bulletin of mathematical biology 40 (1978), S. 499-512 
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    Notes: Abstract For the tumor model of Skipper and Zubrod, which has been analyzed previously for the theoretical FLM function and the effect of chemotherapy against tumors of known or assumed kinetic characteristics, the theoretical continuous labeling (CL) function is derived by considering an equivalent tumor (in terms of unlabeled cell populations) in which the density function of phase duration of cells inS-phasef 2(a 2)=δ(a 2−∞) and the loss functionL 2(t)=0. This mathematical concept of blocking is applied to the analysis of synchronization in tumor growth and blocking effects in cancer chemotherapy. These effects of chemical agents on the cell cycle progression are being incorporated into a previously written computer simulation program for cancer chemotherapy. Whereas, a program is written and used to simulate the CL functions for L1210 leukemia, and primary and metastatic Lewis lung carcinoma.
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    Bulletin of mathematical biology 40 (1978), S. 525-533 
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    Notes: Abstract Global stability is established in a class of prey-predator models. This includes a prey-predator model in which the predator has Type 2 functional response and no intraspecific interactions. Two simple examples demonstrate that Kolmogoroff’s theorem does not apply to some members of this class of models.
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    Bulletin of mathematical biology 40 (1978), S. 535-540 
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    Notes: Abstract The skeletal muscle is regarded as a periodically deformed plate. An equation of energy for the biological tissue in the system is used in the Lagrange variables. With the heat exchange through the above tissues to the exterior media and also with account of some relations between the physiological factors the approximate analytical solution for this equation is obtained and compared with the physiological data.
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    Bulletin of mathematical biology 40 (1978), S. 541-545 
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    Notes: Abstract One of Bobisud's (1976) models for the evolution, of cannibalism is discussed. His analysis is criticised for not being based on the principle of individual selection. Assuming the operation of that principle, we show by simulating his model that cannibals may establish themselves in a noncannibal population. This will happen both in cases where Bobisud concluded cannibalism to be optimal and in cases where he concluded cannibalism not to be optimal.
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    Bulletin of mathematical biology 40 (1978), S. 547-547 
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    Bulletin of mathematical biology 40 (1978), S. 549-579 
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    Notes: Abstract The D'Arcy Thompson concept of biological transformations is developed in a form analogous to such physical concepts as the Law of Corresponding States in thermodynamics, and the Principles of Similitude found in engineering. We find that such concepts depend on a distinction between fundamental and derived quantities, in which the values assigned to the fundamental quantities set the natural scales for the derived ones. Among other things, we see that critical phenomena, such as phase transitions, arise as an immediate consequence of this distinction. In a biological context, we explore the implications of Thompson's hypothesis that closely related organisms are phenotypically similar, assuming that the organisms we see are the result of selection processes operating on phenotypes.
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    Bulletin of mathematical biology 40 (1978), S. 605-623 
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    Notes: Abstract If information is coded in the combination of activities of many neurons operating in parallel, then information present in a network can be defined by the correlation of present network activity with the activity which had been elicited by a stimulus in the past; a high correlation indicates the presence of the previously encoded stimulus. Information is distributed in the network because coding is dependent upon the activities of all cells. A model based on Hartline-Ratliff lateral inhibition with a time delay shows that lateral inhibition can distribute information across a parallel network, reduce output noise, and also briefly store information. With no changes in model parameters, and the use of a correlation measure for recognition, the model can stimulate psychophysical results in eleven variations of the metacontrast masking paradigm.
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    Bulletin of mathematical biology 40 (1978), S. 581-604 
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    Notes: Abstract A theory is derived to calculate the regional and total deposition of aerosol particles in the nasal passages during inhalation. The particle size studied range from 0.2 to 10.0 μm diameter. The deposition is calculated in five regions; (I) the region filled with nasal hair, (II) the nasal valve, (III) the expansion region, (IV) the turbinate region and (V) the posterior bend. Equations are derived to determine the deposition caused by direct impaction on the nasal hairs and bends of the passages. The calculations show the deposition due to direct impaction does not account for the amount or location of deposited particles measured in experiments. Secondary flows have been speculated to exist in the expansion region after the nasal valve and an equation is derived to estimate the deposition caused by the secondary flows. The calculated deposition, due to direct impaction and secondary flows, shows general agreement with the experiment as to the predicted amount and location of deposited particles.
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    Bulletin of mathematical biology 40 (1978), S. 625-635 
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    Notes: Abstract The paper reviews a series of models for circadian clocks and discusses their conclusions and predictions. Attention is focused on Pittendrigh's empirical model, two mathematical models by the author and Winfree's work.
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    Bulletin of mathematical biology 40 (1978), S. 637-649 
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    Notes: Abstract From a model of facilitated ionic transport across axonal membranes proposed by McIlroy (1975), the equipotentials and electric field distributions in the vicinity of a potassium conducting pore and of a sodium conducting pore are computed and presented as two-dimensional mappings. The model is then extended to include the effect of impurity ions in the conducting pores viz. of potassium ions in a sodium pore and of sodium ions in a potassium pore. The ionic selectivities and permeabilities of the transported species are discussed in relation to the extended model. Bounds are deduced for the ionic selectivity coefficients for both the sodium and potassium current-carrying systems in squid giant axons and the electric-field distributions in the vicinities of the pores are computed for the extended model and compared with the impurity-free fields first calculated. Finally the permeability coefficients defined in terms of the extended model are shown to reconcile the results of attempts to measure permeability by means of radioactive tracer techniques, with the classical description of the resting nerve.
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    Bulletin of mathematical biology 40 (1978), S. 661-669 
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    Notes: Abstract The partial differential equations describing transcapillary exchange and subsequent removal of solutis from an idealized liver sinusoid are amenable to solution by similarity analysis. The power and utility of this technique, which is not widely appreciated as a method for solving biological models, is illustrated here for a system whose Laplace transforms is difficult to invert.
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    Bulletin of mathematical biology 40 (1978), S. 671-674 
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    Notes: Abstract The phenomenological theory for the chemotaxis and consumption of oxygen by motile aerobic bacteria is shown to yield a remarkably simple one-dimensional steady-state solution for a congregation of bacteria close to the surface of an oxygen-depleted aqueous medium.
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    Notes: Abstract In this paper biological compartmental models are considered which take into account the intrinsic randomness of the transport rate parameters and their possible variability in time. An identification procedure is presented for the estimation of the stochastic processes representing the transport rate parameters of a compartmental model from a noisy input-output experiment. The problem is formulated in terms of nonlinear filtering. A simple model is discussed for the case in which the transport rate parameters are independent of each other. The possibility of testing possible important features of the behavior of the transport rate parameters is also evidenced.
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    Bulletin of mathematical biology 40 (1978), S. 853-863 
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    Notes: Abstract For any essentially nonlinear system of reaction-diffusion equations of the generic form ∂ci/∂t=Di∇2ci+Qi(c,x,t) supplemented with Robin type boundary conditions over the surface of a closed bounded three-dimensional region, it is demonstrated that all solutions for the concentration distributionn-tuple function c=(c 1(x,t),...,c n (x,t)) satisfy a differential variational condition. Approximate solutions to the reaction-diffusion intial-value boundary-value problem are obtainable by employing this variational condition in conjunction with a Galerkin-Ritz procedure. It is shown that the dynamical evolution from a prescribed initial concentrationn-tuple function to a final steady-state solution can be determined to desired accuracy by such an approximation method. The variational condition also admits a systematic Galerkin-Ritz procedure for obtaining approximate solutions to the multi-equation elliptic boundary-value problem for steady-state distributions c=−c(x). Other systems of phenomenological (non-Lagrangian) field equations can be treated by Galerkin-Ritz procedures based on analogues of the differential variational condition presented here. The method is applied to derive approximate nonconstant steady-state solutions for ann-species symbiosis model.
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    Bulletin of mathematical biology 40 (1978), S. 873-875 
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    Bulletin of mathematical biology 41 (1979), S. 129-138 
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    Notes: Abstract The results of an earlier effort to provide a geometrical analysis of Hutchinsonian niche space are extended. The concept of diversity of a species in niche space is introduced and the maximization of this diversity provides a rationale for a within-niche fitness distribution which is Gaussian. Niche expansion is seen as a consequence of diffusion in niche space, and an evolutionary version of the Volterra competition equations is proposed as a way to relate niche geometry with population dynamics. Applications to topics in community evolution, species packing and the statistical fitting of species abundance data are mentioned.
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    Bulletin of mathematical biology 41 (1979), S. 203-215 
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    Notes: Abstract In this paper we use marginal probabilities to derive expressions for the means, variances and covariances ofm-compartment systems. We also present an efficient algorithm for the estimation of the parameters of the system using time series data when measurements are available fromk of them compartments. An application of the analysis and parameter estimation procedure for a model representing the results of a cancer treatment follow-up study is given.
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    Bulletin of mathematical biology 41 (1979), S. 193-201 
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    Notes: Abstract The self-organizing properties of an ensemble of interconnected units are studied by linear stability analyses. Small perturbations of a uniform steady-state may result in bifurcations to other solutions that exhibit spatial or temporal order. We show that increasing the number of connections that a unit makes with its neighbors changes the nature of these solutions and tends to destroy spatiotemporal patterns. If an unconnected system is orginally stable, the formation of multiple interconnections can never induce temporal periodicity but may, under certain circumstances, allow the emergence of stationary spatial patterns. We have verified the predictions of the linear stability analysis on a model system and comment on the implications of these results for multicellular ensembles.
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    Bulletin of mathematical biology 41 (1979), S. 217-227 
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    Notes: Abstract A performance criterion and weighting factors for the optimal cardiac assistance are investigated by applying Tellegen's network theorem and tolerance analysis on animal experimental data for left ventricular (LV) bypass on the failing heart. Two major factors with respect to cardiac assistance (total power delivered to the peripheral circulatory system, and changes in temporal pattern of ventricular contraction) are represented by two performance criteria,J 1 andJ 2 whereJ 1 relates to the sum of LV and pump power, andJ 2 relates to the “peakedness” factor of LV power. The total performance index (J) is determined as the weighted sum ofJ 1 andJ 2;J=w 1J1+w2J2. The weighting factors,w 1 andw 2, are computed as inverses of the tolerance in the performance contours with respect to improvement of stroke work per minute from pre- to post-bypass condition.
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    Bulletin of mathematical biology 41 (1979), S. 253-255 
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    Bulletin of mathematical biology 41 (1979), S. 229-251 
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    Notes: Abstract In treating the Volterra-Verhulst prey-predator system with time dependent coefficients, we ask how far this deterministic system represents or approximates the dynamics of the population evolving in a realistic environment which is stochastic in nature. We consider a stochastic system withsmall Gaussian noise type fluctuations. It is shown that the higher moments of the deviation of the deterministic system from the stochastic approach zero as the strength δ of the perturbation decays to zero. For any δ〉0 and allT〉0, ε〉0, the sample population paths that stay within ε distance from the deterministic path during [0,T] form a collection of positive probability. In comparing the stationary distributions of the two systems, we show that the weak limits of those of the stochastic system form a subset of those of the deterministic system. This is in analogy with a result of May connected with the stability of the two systems. Plant and rodent populations possess periodic parameters andexhibit periodic behaivor. We establish theoretically this periodicity under periodicity conditions on the coefficients and perturbing random forces. We also establish a central limit property for the prey-predator system.
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    Bulletin of mathematical biology 41 (1979), S. 257-282 
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    Notes: Abstract Adaptation of repetitively firing sensory neurons and nerve models is correlated with specific inhibitory feedback phenomena—an electrogenic sodium pump, and post synaptic self inhibition. The quality of the adaptive responses depends on the excitation properties of the neuron in the interspike interval, or the description of these properties by the underlying impulse encoder model. THis model dependence is demonstrated by comparisons of the behavior of two classes of models; the “leaky integrator models” which assume a passive neural membrane, and the “variable-γ models”, for which the neural state of excitation varies according to first order differential equations. The complexity inherent in the variable-γ models is effectively boiled down to mathematically simple relationships which are derived from studies of the neural- and model frequency responses to small amplitude sinusoidal stimuli. It is argued, and supported with examples, that these relationships hold for impulse frequency transients resulting from more general stimulus conditions. Expressions are then derived which permit feedback parameters to be determined from impulse frequency data. In this connection, recent studies of neural dynamics are brought to bear to resolve ambiguities in data interpretation.
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    Bulletin of mathematical biology 41 (1979), S. 283-304 
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    Notes: Abstract A setQ(n) of noncongruent connected shapes, constructed from a fixed numbern of congruent regular hexagons laid edge to edge, is defined. Various measures of shape are applied toQ(n) and the results are numerically analyzed in the special casesn≦9. The concept of spatial entropy is introduced which affords a measure of the “complexity” of shape. Possible biological applications include the analysis of ecological cover,stigmergy or the complex nest-building activities of social insects and morphogenesis. Essentially any comparative study of shape, regardless of the specific application, might be carried out along the lines suggested in the paper.
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    Bulletin of mathematical biology 41 (1979), S. 305-324 
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    Notes: Abstract This paper uses optimal control theory in conjunction with a Gompertzian type model for cellular growth to determine the optimal method of administering cycle non-specific chemotherapy or more generally the optimal durations of treatment and rest periods during chemotherapy. The performance critera employed to determine the relative merits of the therapy include not only the destruction of malignant cells, but also the sparing of a critical normal tissue. Since these criteria are at odds with one another, the solutions are found which satisfy the Pareto optimality conditions.
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    Bulletin of mathematical biology 41 (1979), S. 325-342 
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    Notes: Abstract Oscillations governed by generalized Volterra-Gause-Witt equations to include retardation effects in population dynamics are considered. Models containing either small or significant time delay are discussed. The Krylov-Bogoliubov-Mitropolskii perturbation method and its extension for differential equations with retarded argument is used.
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    Bulletin of mathematical biology 41 (1979), S. 357-364 
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    Notes: Abstract A general solution to the dynamical equation for the probability distribution associated withn interacting species is obtained by employing the author's generic canonical expression for the rate functions. Interacting species models with limit-cycle dynamics and no stable equilibrium points feature probability distributions that are asymptotic for large values oft to Dirac δ-distributions concentrated on the limit-cycles, as illustrated here for an analytically solvable two-species model. For ann-species Volterra model, a stationary or temporally-averaged probability distribution should generally be much more complicated than the specialized Poisson form studied by Kerner and others.
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    Bulletin of mathematical biology 41 (1979), S. 365-385 
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    Notes: Abstract A set of coupled nonlinear differential equations, determining the concentration profiles and electric potentials valid for isothermal transport of ions and molecules across a diffusion barrier are formulated, using a correction to the limiting expression for chemical potential gradients and the molecular expression for frictional force. These differential equations are similar to Nernst-Planck equations and reduce to these under appropriate approximations. Solutions of these equations valid under specified conditions are presented. Expressions for permeability, concentration profiles of many ion systems are included.
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    Bulletin of mathematical biology 41 (1979), S. 629-640 
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    Notes: Abstract The global flow equations of nonequilibrium thermodynamics for a single nonelectrolyte solute and water passing through a membrane are obtained by solving the local equations of motion. The method follows that developed for the general,n-solute case in the previous paper (Mikulecky, 1978). It is easily seen in this simple case that the passage from local interactions, formulated as position dependent frictional interactions in the equations of motion, to ghe global result involves a loss of any simple way of identifying particulars about local information. Two particular cases are analyzed in further detail: the case of no interaction within the pore and the case of constant interaction for both solute and solvent across the pore. In the former case, Onsager reciprocity survives in the global result if a self-consistent definition of the partial viscosity coefficients is used, while in the latter case, reciprocity is lost. Since, in many biologically interesting cases, the presence of interaction of the type considered here is likely to occur, the reciprocity condition should not automatically be assumed to hold.
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    Bulletin of mathematical biology 41 (1979), S. 665-686 
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    Notes: Abstract This study is related to a model describing the behavior of barium-treatedAplysia neurons generating regular burst-plateau patterns. The model is represented by an autonomous dynamical system, defined inR 4 and depending on a small parameter. This paper is restricted to the qualitative study of three “reduced systems” deduced from the “complete system”. Part of the study is performed with the use of the qualitative theory of singular perturbations. The predicted behaviors are compared with experimental results.
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    Bulletin of mathematical biology 41 (1979), S. 641-664 
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    Notes: Abstract Using linear stability analysis, the qualitative stability properties of open nonlinear chemical systems, in which reactions of any order may occur, will be studied. Systems will be classified in three fundamental classes: trees, cycles and loops, according to their knot graphs. The study of the Jacobian matrix for the kinetic equations of the system shows that the symmetrizability by a particular procedure (calledD-symmetrizability) is a sufficient condition for stability. It has been proved that tree-graphs always satisfy the above condition. For the cycle-graphs, theD-symmetrizability condition leads to a cyclic relation between forward and reverse steady state flows. The stability may be assured, even if the cyclic relation is not satisfied, providing that the “symmetry breaking” be lower than an upper bound; further alternative criteria for stability of cycles have been derived. All these results are independent of the number of diffusive exchanges with the environment.
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    Bulletin of mathematical biology 41 (1979), S. 687-705 
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    Notes: Abstract The basis of an analytical description of the behaviour of large random nets of binary elements of the type first investigated in detail by S. A. Kauffman is presented. It is shown that information about the network dynamics can be deduced from quite general considerations of the properties of the state transition graph and matrix. An expression for the matrix elements of the state transition matrix in terms of the Boolean function specification of the net is derived. Using these ideas the distribution of limit cycle lengthsl for a completely random net is calculated and shown to bex 1/l, a result which agrees well with experimental data.
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    Bulletin of mathematical biology 41 (1979), S. 707-724 
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    Notes: Abstract The state-transition matrix description of Kauffman binary networks described in the previous paper is further developed to obtain an analytical expression for the fraction of states involved in limit cycles as a function of the network size and connectivity. The result obtained for totally connected networks agrees with that derived from quite different considerations by other workers. For low connectivity networks the results are in qualitative agreement with the experimental data of Kauffman but there is a quantitative discrepancy which remains to be resolved.
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    Bulletin of mathematical biology 41 (1979), S. 877-891 
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    Notes: Abstract Persistence-extinction in simple food chains modelled by Lotka-Volterra dynamics is governed by a single parameter which depends upon the interspecific interaction coefficients, the intraspecific interaction coefficients, and the length of the food chain. In persistent systems with nonzero carrying capacity, two new features predominate. Trophic level influence factors relate persistence on different trophic levels and determine, in conjunction with the persistence parameter, the magnitude of persistence. Equilibrium component ordering, which results in persistent systems, mandates once again that systems need to be studied on the complete ecosystem level; static field measurements reflect species location in the food chain, the total length of the food chain and assume characteristics according to these factors.
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    Bulletin of mathematical biology 37 (1975), S. 97-100 
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    Bulletin of mathematical biology 37 (1975), S. 1-9 
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    Notes: Abstract The study of systems exhibiting a band-pass function is completed for systems whose parameters are time-dependent. In the case of periodic parametric excitations, it is demonstrated that some systems can get into “resonance” for a particular frequency. By studying this problem, a new and probably fruitful approach of some rhythmic behaviours can be made.
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    Bulletin of mathematical biology 37 (1975), S. 19-35 
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    Notes: Abstract Analytical techniques are developed which permit objective control of asiist device driving systems. In addition to being objective, the techniques described in this paper are optimal in the sense of minimizing a performance index which consists of a term involving left ventricular power and a term involving deviations of aorta hemodynamic parameters from normal values. Comparisons are included of off-line computations and measurements on dogs with experimentally induced myocardial infarctions undergoing intraaortic balloon pumping.
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    Bulletin of mathematical biology 37 (1975), S. 427-458 
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    Notes: Abstract A mathematical model simulating a cell growing in a culture medium is obtained. Using this model, various behavioral patterns of the cell are obtained under different types of disturbances, in particular when (i) a Mg2+ deficiency experiment and, (ii) a split-dose ionizing radiation experiment are carried out, (iii) when disturbances on the rate constants of the biochemical reactions taking place in the nucleus of the cell are applied, and (iv) when the cell's interior components are perturbed. The cell model results obtained agree well with experimental results for the Mg2+ and split dose experiments, and explain the mechanism of the split dose radiation experiment without the need to introduce additional axioms (e.g. healing processes) into the dynamics of the cell. Conditions are obtained which cause the cell to behave in a rapidly growing ‘tumor-like’ mode; it is shown that once the cell moves into this ‘tumor-like’ mode, its behavior is irreversible, i.e. if a disturbance of opposite type is then applied to the ‘tumor’ cell, the cell will not revert back to its original normal behavior.
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    Bulletin of mathematical biology 37 (1975), S. 85-90 
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    Notes: Abstract Solution of the equation that describes simulatenous liquid flow and diffusion in a spherical model of the vitreous body of the eye shows that a small dissolved specie can move both anteriorly and posteriorly from a source behind the lens even though there is a slow liquid movement almost entirely in the posterior direction. This results explains why tracer studies using large particles (dyes or colloids) show only a posterior flow, whereas studies using sodium ion show anterior movement as well.
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    Bulletin of mathematical biology 37 (1975), S. 101-107 
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    Bulletin of mathematical biology 37 (1975), S. 111-111 
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    Bulletin of mathematical biology 37 (1975), S. 221-221 
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    Bulletin of mathematical biology 37 (1975), S. 255-268 
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    Notes: Abstract The equations relating hybridized RNA to free RNA, in the case of simple hybridization, or to ratio of labelled and unlabelled RNA in competitive hybridization, are derived. Analysis of the equations shows how hybridization data may be used to infer properties of the distribution of components in an RNA mixture, or the relation between two distributions in competitive hybridization. A critical examination of the assumptions underlying the equations indicates that some of then may be violated in certain cases, or have no current support, evidential or theoretical. The consequences of such qualifications for the interpretation of hybridization data are indicated.
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    Bulletin of mathematical biology 37 (1975), S. 589-636 
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    Notes: Abstract The steady state spatial patterns arising in nonlinear reaction-diffusion systems beyond an instability point of the thermodynamic branch are studied on a simple model network. A detailed comparison between the analytical solutions of the kinetic equations, obtained by bifurcation theory, and the results of computer simulations is presented for different boundary conditions. The characteristics of the dissipative structures are discussed and it is shown that the observed behavior depends strongly on both the boundary and initial conditions. The theoretical expressions are limited to the neighborhood of the marginal stability point. Computer simulations allow not only the verification of their predictions but also the investigation of the behavior of the system for larger deviations from the instability point. It is shown that new features such as multiplicity of solutions and secondary bifurcations can appear in this region.
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    Bulletin of mathematical biology 40 (1978), S. 1-25 
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    Notes: Abstract The geometrical nature of the Elementary catastrophes (Thom, 1969) is reviewed. Histories of the movement of catastrophe manifolds and bifurcation sets are presented for some of the space-equivalent unfoldings described by Wassermann (1975). These unfoldings provide descriptions of the variation with time of the stability of stationary states of associated potential energy functions. Identification of these stationary energy states with stationary states of a system therefore provides a description of its behavior with time. Qualitative descriptions of this type are particularly useful when the complexity of a system prevents a detailed quantitative description. Histories of bifurcation set movements suggest different types of system behavior at different space-like coordinates. This type of theory may be a useful model for the processes leading to differentiation of cells and to emergence of adult forms of a biological organism.
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    Bulletin of mathematical biology 40 (1978), S. 27-44 
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    Notes: Abstract Three conjectures are given which predict the existence of unique stable limit cycle oscillations in a class of piecewise linear (PL) differential equations. The equations are appropriate to model biological or other complex systems in which there are switchlike interactions between the elements of the network. Methods are presented which can be used to develop mathematical models which are conjectured to display stable limit cycle oscillations, from qualitative experimental information about relative phases of activity in the dynamical systems. Several illustrative numerical examples are given, and one experimental example from neurobiology is discussed.
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    Bulletin of mathematical biology 40 (1978), S. 79-93 
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    Notes: Abstract The formulation and results of the Kalman State Regulator Problem are applied to a mathematical model of the arterial system of a dog to obtain an optimal control for blood pressure. The criterion for optimality is minimum energy per cycle.
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    Bulletin of mathematical biology 40 (1978), S. 95-105 
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    Notes: Abstract A mathematical model is developed in state variable form suitable for the study of the control of blood pressure and flow in the mammalian cardiovascular system. The applicability of the model to steady state, both mean and pulsatile, and transient phenomena is demonstrated by the agreement of the results with experimental data. This model was developed to study the neural and renal-endocrine-electrolyte control of cardiovascular functions.
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    Bulletin of mathematical biology 40 (1978), S. 133-160 
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    Notes: Abstract As a contribution to the discussion of oscillatory models for interacting species it is shown that two-species Volterra models can never have limit cycles, and a complete enumeration is given of conditions which the parameters of these models must satisfy in order that a part of the phase space be filled with a family of closed curves; sketches of phase portraits are also given. These results complement and correct older results by Bautin and by Coppel on quadratic differential systems. The paper opens with a brief discussion of some more practical aspects of the ecological application of oscillatory models.
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    Bulletin of mathematical biology 40 (1978), S. 107-121 
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    Notes: Abstract The purpose of this paper is to present a method for the determination of a solution for a coupled system of first order initial boundary-value problems arising from some biological systems. The physical problem is to determine the suspended and the superficial molecular concentrations of a traced substance passing through an organ containing a tangle of vessels, such as the kidney-ureter system. The approach to the problem is by successive approximation which leads to a recursion formula for the determination of the solution as well as error estimates for the approximations. The recursion formula involves only direct integration which indicates a promising possibility in obtaining numerical results by using a computer. In addition to the determination of a solution, some qualitative analysis of the solution is given. This includes the existence of a unique solution, the continuous dependency of the solution on the data, and the stability problem of a steady-state solution.
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    Bulletin of mathematical biology 40 (1978), S. 183-199 
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    Notes: Abstract In Part I, the general solution of the heat transport equation was given for a medium of constant thermal properties, containing a general convection fieldv(r,t). Starting from this general solution, an average or “macroscopic” temperature distribution is calculated in this paper, since in most physiological problems only an average or “macroscopic” temperature is accessible to the measurement. It is shown that the averaged temperature distribution is influenced alone by the order of the local symmetries of the convection field. These local symmetries can be deduced from anatomical data on the vascular architecture. In order to perform the averaging process, a detailed discussion, and an estimate of the correlation between the microscopic temperature variation and the convection field is carried out. Hereby, great emphasis is put on the experimental consequences of these results. As an illustrative example, the calculation of the macroscopic temperature distribution in a medium traversed by parallel capillaries is outlined.
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    Bulletin of mathematical biology 40 (1978), S. 201-209 
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    Notes: Abstract The study of current flow fields in biologicaltissue requires finding the potential field from dipole sources such that the normal gradient vanishes at the exterior surface. A convenient way to determine the dipole field is by taking the gradient of the potential field set up by a point source. However, the point source problem is ill-posed when the normal gradient is required to vanish at the outer surface. In the paper the nature of this problem is discussed and several methods for overcoming the difficulty are presented.
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    Bulletin of mathematical biology 40 (1978), S. 223-235 
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    Notes: Abstract An analysis of the hydrodynamics of aqueous flow in the posterior chamber of the anterior segment of the eye is presented. The viscid, incompressible description of fluid dynamics in a spherical geometry is utilized to reduce the problem to a biharmonic-type equation using a “Stokes Stream Function”. Analogous to Poiseuille flow in a cylindrical pipe, velocity profiles are deduced and an Ohms Law relationship between pressure and flow is derived in terms of the geometry of the assumed model. This result is then incorporated into a synthesized electric circuit analog of flow between ciliary artery and episcleral vein. Applications to open angle and pupilary block glaucoma are discussed.
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    Bulletin of mathematical biology 40 (1978), S. 247-255 
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    Notes: Abstract With the assumption of dipole interaction with the membrane matrix, the dipole barrier under an applied field shows a minimum in its time transient. Kinetic equations governing the migration of ions are presented. Na+ activation, Na+ inactivation and K+ delay are all part of the same mechanism in this model with no other separate assumptions needed. Voltage Clamp equation and action potential equation are presented.
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    Bulletin of mathematical biology 40 (1978), S. 265-269 
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    Notes: Abstract A metabolic model for copper is derived and presented in the context of the International Commission on Radiological Protection (ICRP) dosimetry models for the lungs and gastrointestinal tract.
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    Bulletin of mathematical biology 40 (1978), S. 257-264 
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    Notes: Abstract The analytical conditions by which a Volterra's general system describingn interacting species can be put in the “conservative” form have been examined. The cases forn=2, 3, 4 have been analyzed in detail and a general condition for any value ofn is deduced. The analytical and biological constraints following by this approach are compared to the conclusions drawn by Leigh on the ground of purely biological considerations.
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    Bulletin of mathematical biology 40 (1978), S. 237-246 
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    Notes: Abstract General formulation of stochastic single- and multi-compartment reversible systems with time-dependent transitions is made. The correspondence between the stochastic mean and the deterministic value is established in case of time-dependence and it is shown how the consequence of this can be utilized to compute the distribution and the moments of each individual compartment of the system. A two-compartment reversible system previously proposed by Cardenas and Matis (1975a) is analyzed on the basis of the theory.
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    Bulletin of mathematical biology 40 (1978), S. 271-272 
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    Bulletin of mathematical biology 40 (1978), S. 319-333 
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    Notes: Abstract Optimal control theory is applied to the problem of controlling pests by biological and chemical means simultaneously. The net birth rate of the pests is controlled chemically while at the same time predators are allowed to operate. Several numerical examples are included.
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    Bulletin of mathematical biology 40 (1978), S. 273-300 
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    Notes: Abstract Transient solutions are developed for the buildup of a concentration gradient in the single loop solute cycling model of the renal medulla. The “pump” from ascending limb to descending limb is considered in both unsaturated and completely saturated modes of operation. Both analytic solutions and semianalytic solutions obtained from inverting Laplace transforms are considered. The classic representation of concentration buildup by the multiplication process is compared with calculated profiles. The “single effect” is found to vary both in time and space.
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    Bulletin of mathematical biology 40 (1978), S. 335-345 
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    Notes: Abstract In this study the possibility of applying the asymptotic method of Krylov-Bogoliubov-Mitropolskii to problems of population dynamics is shown. Especially a general Volterra-Gause-Witt type model for prey-predator interaction is investigated. A discussion on the results obtained is given for the general model and for a particular case as well.
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    Bulletin of mathematical biology 40 (1978), S. 301-318 
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    Notes: Abstract The analytical exploration of hierarchical structures is a central problem in modern biology. In many ways, the most basic tenet of any theory of any biological system is that its behavior lies within the laws of thermodynamics. Thus an investigation into the hierarchical structure of field thermodynamics is in effect an investigation into the underlying structures common to all biological systems. In field thermodynamics, the dynamics is prescribed at the hierarchical level of description concerned with the motions of classes of the various molecular species flowing in the system. Of crucial importance are scale factors which convert potentials into potential energies per mole of the various molecular species. On the other hand, the overall behavior of the system is presented at a higher hierarchical level of description in terms of systemic properties such as charge density or entropy density. Three questions are investigated: (1) how is the transition from the specific to the systemic level of description effected, (2) given the scale factors at the specific level how does one find those at the systemic level, and (3) what relationship can one, find between the scale factors at the two levels of description? Answering these questions necessitates an examination of the nature of the forces at the two levels of the hierarchy of descriptions.
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    Bulletin of mathematical biology 40 (1978), S. 369-376 
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    Notes: Abstract The identification of a linear compartment model, which may describe a chemical or biological process, is a difficult task, since the available data is generally limited. In this paper we propose a method for determining the state transition matrix by minimizing a given quadratic criterion. To solve the resulting matrix equation, an assumption has to be made which constitutes a necessary condition for the identifiability of the model. Moreover when this assumption is satisfied, it is shown that the knowledge of one line or one column of the transition matrix is sufficient to define it completely.
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    Bulletin of mathematical biology 40 (1978), S. 359-368 
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    Notes: Abstract The two-element muscle model considered consists of a contractile element defined by a hyperbolic force-velocity relation connected in series with an “exponential spring”. Differential equations for the isometrically developed force during a tetanic contraction and the corresponding contractile element shortening velocity are derived and their stability is investigated. Analytical solutions to both equations are obtained. Two numerical examples are given, the second chosen to illustrate pressure-induced hypertrophy of a cardiac muscle.
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    Bulletin of mathematical biology 40 (1978), S. 347-358 
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    Notes: Abstract We study a two-type, age-dependent branching process in which the branching probabilities of one of the types may vary with time. Specifically this modification of the Bellman-Harris process starts with a Type I particle which may either die or change to a Type II particle depending upon a time varying probability. A Type II particle may either die or reproduce with fixed probabilities but may not return to a particle of Type I. In this way the process models the lag phenomenon observed in microbe growth subsequent to transfer to a new culture medium while the organism is adapting to its new environment. We show that if the mean reproduction rate of Type II particles exceeds 1, then the population size grows exponentially. Further the extinction probability for this process is related to that of the Bellman-Harris process. Finally the governing equations are solved for several choices of the growth parameters and the solutions are graphically displayed showing that a wide variety of behavior can be modeled by this process.
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    Bulletin of mathematical biology 40 (1978), S. 377-385 
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    Notes: Abstract This paper studies the effect of harvesting a fraction of a population where the population growth is modelled by a linear age-dependent model, the Von Foerster equation. Two harvesting strategies are considered: the first is where a fraction of the population greater than agec is removed, and the second is where a fraction of the population of age greater thanc but less thanc+n is removed. In the case where the death rate and fertility rate are time independent, the effect of harvesting on the stable age distribution is examined.
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    Bulletin of mathematical biology 40 (1978), S. 425-426 
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    Bulletin of mathematical biology 40 (1978), S. 387-410 
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    Notes: Abstract The general means are set forth by which, in a highly speciated Volterra eco-system, the bifurcation of a species into two in a competitive-exclusion configuration, provides a description of odd as well as even systems. The the Gibbs ensemble theory earlier developed is extended to grand ensembles in which the number of ecotypical species in genera-like clusters is allowed to be variable. The probability law for the sizes of clusters is deduced, and shown very closely to imply independent Poisson statistics for the cluster sizes, in answer to a fundamental issue of bioevolution. The role of the eco-analogs of Gibbs’ chemical potentials is brought forth, with a suggestion of how to describe cluster-to-cluster eco-genetic flows, and therewith a definite relationship between the degrees of speciation of genetically linked clusters on the one hand, and amplitudes of population fluctuations of member species within the clusters on the other hand.
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    Bulletin of mathematical biology 40 (1978), S. 427-427 
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    Bulletin of mathematical biology 40 (1978), S. 411-424 
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    Notes: Abstract Solutions of the Poisson-Boltzmann equation yield potential profiles and equilibrium distributions of ions on either side of a spherical shell membrane across which there exists a separation of ionic charges. For the special case in which the membrane is permeable to only one ion the total charge separation is analyzed in terms of the potential difference given by the Nernst equation. Potential profiles and ionic charge distributions are also given for situations involving a uniform distribution of fixed charges within the membrane.
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    Bulletin of mathematical biology 40 (1978), S. 429-450 
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    Notes: Abstract The recently proved classification theorem of René Thom has led to the development of the new science of Catastrophe Theory. This theory has been widely held to be particularly relevant in biological applications. The present paper presents a simplified proof of Thom’s Theorem and assesses its importance in biology.
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    Bulletin of mathematical biology 40 (1978), S. 451-464 
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    Notes: Abstract A mathematical model describes the mechanical behaviour of ventricular aneurysms assuming a spherical geometry for the left ventricle. Employing pressure-volume data obtained from normal dog hearts 1–2 hours after infarction, conditions are obtained on infarct thickness and angle of damage for ventricular rupture to occur. The results indicate that rupture is more likely to occur in the early period following infarction and that the dominant factor is the per cent thickness of the infarct.
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    Bulletin of mathematical biology 40 (1978), S. 483-498 
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    Notes: Abstract A deterministic investigation of a linear differential equation system which describes predator vs prey behavior as a function of equilibrium densities and reproductive rates is given. A more realistic structure of this model in a stochastic framework is presented. The reproductive rates and initial population sizes are considered to be random variables and their probabilistic behavior characterized by various joint probability distributions. The deterministic behaviors of the prey and predator species as functions of time are compared with the mean behaviors in the stochastic model.
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    Bulletin of mathematical biology 40 (1978), S. 465-482 
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    Notes: Abstract The effects of ventricular geometry, muscle mass, muscle elasticity and external pressures on the pressure-volume and muscle stiffness-stress relations have been quantitated on the basis of a theoretical model. Data taken from patients before and after interventions with nitroprusside and angiotensin were applied to the model in order to explain the possible causes for the marked shifts in the pressure-volume relations. The results indicate that (a) ventricular geometry does not markedly alter the pressure-volume and stiffness-stress relations unless there is a drastic change from a spherical shape to an ellipsoidal shape orvice versa, (b) increases in muscle mass and muscle elasticity of the order of 30% result in significant alterations in the P-V relations but are not the cause for the parallel shifts unless accompanied by substantial external pressures, (c) the parallel shifts in the pressure-volume relations can be accounted for entirely by the presence of external pressures without changes in muscle mass or muscle elasticity. Thus manipulation of right ventricular pressures or pericardial pressures by drug interventions may be useful in the treatment of left heart disease and the presence of such pressures must be considered in the analysis of ventricular function curves.
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    Bulletin of mathematical biology 40 (1978), S. 675-692 
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    Notes: Abstract This paper summarizes in a nonmathematical way the major properties of coupled oscillators which relate to circadian rhythms. For certain values of the coupling strength it is far easier to maintain synchrony than to achieve it among the various interacting units. This property not only simulates the free run period lability but also the effects of critical pulses.
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    Bulletin of mathematical biology 40 (1978), S. 707-718 
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    Notes: Abstract A deterministic model for a multi-agent disease epidemic with asymptomatic attacks is proposed and investigated. The limitations inherent in the assumptions of the model are discussed in connection with specific agents of disease. The mathematical treatment of the model is separated into analyses of the equilibrium situation and the transient behavior of the disease outbreak. Explicit formulas are derived for the number of susceptibles in the population as well as for the numbers of each type of infective—those with and without symptoms. These theoretical results are followed by a discussion of the practical considerations which must be taken into account to obtain useful information from the model.
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    Bulletin of mathematical biology 40 (1978), S. 719-726 
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    Notes: Abstract The recently observed enhancement, by laser irradiation, of the specific activity of the enzyme chymotrypsin (which hydrolyses Benzoyl-L-tyrosine-ethyl ester) at low enzyme concentration is considered. The enhancement of the reaction rate is attributed to a coherently excited state of the enzyme molecule (activated through Raman scattering of the laser light) following a prediction due to Fröhlich. The model is described, the kinetics of the process is framed and the observed enzyme-concentration dependence of the specific activity is reproduced. Predictions of the model are delineated to urge verification of the main contentions through further experimentation.
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    Bulletin of mathematical biology 40 (1978), S. 693-706 
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    Notes: Abstract The deposition of aerosol particles in the human lung airways is due to two distinct mechanisms. One is by direct deposition resulting from diffusion, sedimentation and impaction as the aerosol moves in and out of the lung. The other is an indirect mechanism by which particles are transported mechanically from the tidal air to the residential air and eventually captured by the airways due to intrinsic particle motion. This last mechanism is not well understood at present. Using a trumpet airway model constructed from Weibel's data, a two-component theory is developed. In this theory, the particle concentrations in the airways and the alveoli at a given airway depth are considered to be quantitatively different. This difference in concentrations will cause a net mixing between the tidal and residential aerosol as the aerosol is breathed in and out. A distribution parameter is then introduced to account for the distribution of ventilation. The effect of intrinsic particle motion on the aerosol mixing is also included. From this theory, total and regional deposition in the lung at the steady mouth breathing without pause is calculated for several different respiratory cycles. The results agree reasonably well with the experimental data.
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