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  • Springer  (302,553)
  • Wiley  (59,920)
  • 1975-1979  (255,123)
  • 1960-1964  (107,350)
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  • 1
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    Bulletin of mathematical biology 22 (1960), S. 323-349 
    ISSN: 1522-9602
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract Equations were derived showing the relationship between the membrane potential and the quantities which influence it under steady state conditions. Essentially, the membrane potential is caused by the valence and concentration of the non-permeating ions. The permeating ions can modify the membrane potential by altering the relative concentration of the non-permeating ions with respect to the concentration of the permeating ions. For muscle, the sodium cations act as the non-permeating ions in the extracellular environment by the maintenance of some type of active metabolic process and large anions act as the non-permeating ions in the intracellular environment. Both of these non-permeating ions contribute about equally to the maintenance of the resting membrane potential. When the active metabolic process for sodium extrusion breaks down or when acids are added, the membrane potential should decrease. Water should enter the cell when the sodium metabolic process is diminished; water should leave the cell when acids are added. When acid is added, it is expected that the cations potassium and sodium will leave the cell with little or no shift of the chloride ions.
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  • 2
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    Bulletin of mathematical biology 22 (1960), S. 351-364 
    ISSN: 1522-9602
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    Notes: Abstract A purely information-theoretical approach to the problem of self-replication of elementary living units implies that pure chance is the determining factor in the formation of the first living unit. The probability of such a spontaneous formation can be calculated from the minimum amount of information which an organism must possess in order to replicate itself. An estimation of this amount of information is made here by two different methods. First by a “paper and pencil experiment” which indicates the minimum amount of information needed on a printed page in order that with given tools the page could be reproduced. Second—by an analytical consideration of some hypothetical molecular mechanisms. A general method for handling such problems is suggested. On the basis of estimated information contents it is shown that under most favorable conditions the probability of a spontaneous generation by pure chance during the lifetime of the earth is vanishingly small. It is concluded that dynamic factors, which may reduce tremendously the information content, must play a role in the genesis of life on earth.
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    Bulletin of mathematical biology 22 (1960), S. 365-370 
    ISSN: 1522-9602
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    Notes: Abstract The binding energy of a very long molecular chain, composed of different classes of molecules, depends in general on the order of the molecules. It is shown that under very general conditions there exists for a givenbrutto chemical composition of a chain, a class of chains which is characterized by a total binding energy which is equal to the total binding energy of any other prescribed chain of different composition within the limits of unsharpness of the energy level. This establishes a criterion formapping of a class of configurations of long chain molecules on another class. To the extent that a mapping constitutes a generalized code those results contribute to the theory of molecular codes. Applying to our results the results of a previous paper (1959,Bull. Math. Biophysics,21, 309–326), we arrive at the conclusion that the self-replication of a living molecule may be the property not of a particular structure but of classes of structures.
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  • 4
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    Bulletin of mathematical biology 22 (1960), S. 371-389 
    ISSN: 1522-9602
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    Notes: Abstract Making some plausible assumptions about the over-all mechanism of food catching and consumption by fishes and evaluating in the light of those assumptions some available experimental data, it is possible to calculate from those data the variation of several important factors with the concentration of food. The factors considered are: total rate of metabolism, total diurnal energy expenditure in the process of feeding, average number of hours per day during which the fish feeds, average length of path traveled by a fish per day, and the so-called “energetic coefficient of growth.” A possible relation with the work of N. Rashevsky (Bull. Math. Biophysics,20, 299–308, 1959) is discussed.
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  • 5
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    Bulletin of mathematical biology 22 (1960), S. 425-425 
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    Bulletin of mathematical biology 22 (1960), S. 417-424 
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    Notes: Abstract The theory of measurement of flow and volume by indicator dilution techniques is given in conditions of time-variable flow rates. It is shown that the usual Hamilton (1932,Am. J. Physiol.,99, 534–551) methods can be misleading if the flow changes at a rate of close to that of the transport function.
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  • 7
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    Bulletin of mathematical biology 23 (1961), S. 305-318 
    ISSN: 1522-9602
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    Notes: Abstract Freese’s Hypothesis states that a single specific alteration in the sequence of nucleotides of an information-bearing DNA molecule results in a specific mutational effect. Within the framework of the DNA-protein coding problem developed elsewhere, and assuming the quasi-ergodicity of the general coding process, it is shown that Freese’s Hypothesis allows us to derive expressions for the length of the smallest mutable DNA molecule and to obtain a bound for the maximal number of allelic molecules of fixed length. To illustrate these ideas, calculations are carried out on appropriate data from bacternophage and man, and the results are shown to differ by a factor of 10 (modulo the rather crude approximations used). It is further shown that, if ρ(N) and ϱ(N) are respectively the number of information-bearing words of lengthN in a given code and the number of words of lengthN, then the number lim ρ(N)/ϱ(N) depends sensitively on the parameter ∈ which specifiesN→∞ the given code. The implications of this result for the spontaneous aggregation of a sufficient number of information-bearing words to characterize an organism are discussed.
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  • 8
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    Bulletin of mathematical biology 23 (1961), S. 319-319 
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    Bulletin of mathematical biology 23 (1961), S. 321-335 
    ISSN: 1522-9602
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    Notes: Abstract As a “base line” of memorization performance, the behavior of a “perfect learner” is considered. He is characterized by a perfect memory and by the ability to choose the best search procedure in problems where the correct response from a given repertoire is to be found to each of several stimuli under the condition of “right” and “wroing” promptings by the experimenter. Expected learning curves are derived for the case of disjoint response repertoires associated with the stimuli under cyclic and random presentation of the stimuli and for the case of a single response repertoire (a one-to-one matching problem) under cyclic presentation.
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  • 10
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    Notes: Abstract Detailed equations are given for the computation of aortic distensibility in the intact living human patient from measurements of systolic and diastolic arterial pressures, heart rate and cardiac output. From these equations, the aortic characteristics of a large series of normal men of different ages were computed. Comparing these results with measurements on excised aortas, a more pronounced trend toward increasing aortic stiffness with increasing age is evident in living than in dead aortas. Nor-epinephrine and exercise apparently cause the living aortas to constrict but to become more distensible. The same change occurs after 30 minutes of high spinal anesthesia. The ganglionic blocking agents hexamethonium, pentamethonium, and tetraethylammonium usually cause the living aorta to become stiffer, presumably due to dilatation. The aortas of patients with pulmonary disease usually react in different fashion to exercise or tetraethylammonium. The increased aortic distensibility that occurs with the hypertension induced by nor-epinephrine or exercise acts as a compensatory mechanism by decreasing systolic pressure.
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    Bulletin of mathematical biology 23 (1961), S. 355-376 
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    Notes: Abstract Dimensional analysis is discussed from the viewpoint of its basic group properties and shown to be an algebraic Abelian group that is useful for analysis of physical measurements. The application of the method to various types of equations and the formulation of previously unclassified dimensions are discussed. Functional dimensional analysis is applied to the problems of cell size and biomass proliferation; future applications are also noted. A number of dimensionless terms have been formulated for cellular physiochemical phenomena. They apparently represent the first systematic study of biological dimensionless numbers recorded in the literature. A dimensionless proliferation law is suggested. A brief analysis of the physical dimensionality associated with information measures is carried out. Entropy and “information” are shown to be completely different in their dimensional meaning; other informational measures of possible interest in biology are proposed. The dimensional coding and computor analysis of biomathematical equations is suggested.
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    Bulletin of mathematical biology 23 (1961), S. 377-391 
    ISSN: 1522-9602
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    Notes: Abstract Expenditure of energy under several simultaneous forms (mechanical, chemical, etc.) is associated with all muscular activity. The energy is directly related to what is commonly called exertion or effort. This paper defines “muscular effort” quantitatively in terms of some of the elements of the dynamics of the human (and animal) body. It postulates that in all likelihood the individual will, consciously or otherwise, determine his motion (or his posture, if at rest) in such a manner as to reduce his total muscular effort to a minimum consistent with imposed conditions, or “constraints”. The principle, formulated in mathematical terms, is sufficient to ascribe to the moments at all body joints—a matter generally of free choice on the part of the individual—their most likely magnitudes. It therefore renders the equations of human (and animal) motion determinate within this context. The paper also describes briefly an iteration method for the solution of these equations, once they have been made determinate. A simple illustrative application of the principle is included.
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    Bulletin of mathematical biology 23 (1961), S. 393-403 
    ISSN: 1522-9602
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    Notes: Abstract It is pointed out that two fundamentally different views of primary genetic processes occur in the literature which are frequently confused. The first is a true communication-theoretic view, which regards the genetic apparatus as containing a real information-source and a transducer which converts that information to useful form. The second view is generally expressed as a template scheme based on the Watson-Crick model; it is shown that in this model there is actually no such thing as genetic information in a communication-theoretic sense. Both views are then discussed on the basis of microphysical principles developed in previous work of the author (Bull. Math. Biophysics,22, 227–255, 1960) in an attempt to find which approach is in closer accord with the biological facts. It is shown that, if the communication-theoretic view is correct, then the information-bearing object must act as a “catalyst,” but it is pointed out that the type of catalysis involved must be of a fundamentally different nature than that occurring in familiar enzyme-catalyzed reactions. On the basis of general considerations of irreversible changes in microphysical measuring systems, it is shown that any type of template must suffer a gradual and irreversible denaturation, which seems to make it unlikely that a template could play a primary role in fundamental genetic processes.
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    Bulletin of mathematical biology 23 (1961), S. 405-411 
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    Notes: Abstract The theory developed in previous papers and based on distribution curves of definite form is generalized to any form of unimodel distributions. The time course of the change from one behavior to another is discussed and a general theorem about the time course is established.
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  • 15
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    Bulletin of mathematical biology 23 (1961), S. 417-417 
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    Bulletin of mathematical biology 25 (1963), S. 471-471 
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    Bulletin of mathematical biology 25 (1963), S. 421-469 
    ISSN: 1522-9602
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    Notes: Résumé Nous appliquons le modèle de neurone introduit dans un article antérieur à l’étude d’une microstructure isotrope. La stabilité de cette microstructure implique l’existence d’une régulation d’activité que le principe de construction adéquate permet de définir entièrement. Nous aboutissons à une conception stratifiée du cerveau. Un réseau de neurones spécialisés exercerait, grâce à certains médiateurs chimiques, une action diffuse qui modulerait les propriétés du réseau localisé classique. Les lois de Pavlov peuvent être retrouvées à partir des propriétés de la microstructure et de celles de la régulation. La microstructure isotrope peut également fonctionner comme analyseur. Un certain nombre de temps caractéristiques apparaissent alors, qui semblent jouer un grand rôle en psychologie.
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    Bulletin of mathematical biology 26 (1964), S. 1-7 
    ISSN: 1522-9602
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    Notes: Abstract In the arteries, blood flow and blood pressure are pulsatile in nature (Roston, 1962a; Roston 1962b). The patterns of blood movement and mural distension in the arteries are important because they may be associated with life-threatening degenerative changes in the arterial walls. As the vascular channels narrow, the pulsation decreases. At the level of the capillaries, almost no pulsation exists (Best and Taylor, 1961). The tissues are affected by the direct flow in the capillaries and not by the pulsation in the arteries. Thus, such quantities as pulse pressure, systolic pressure, and diastolic pressure which characterize blood movement in the arteries are not important as far as the tissues are concerned. Rather, the average pressure and flow in the capillaries are the quantities significant for tissue blood flow. The present study analyzes the local blood circulation in a typical tissue. Logical extension of this analysis results in insights into the physiological behavior of the circulation which integrate a considerable body of experimental data.
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    Bulletin of mathematical biology 41 (1979), S. 893-898 
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    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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    Bulletin of mathematical biology 37 (1975), S. 37-49 
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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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    Bulletin of mathematical biology 37 (1975), S. 59-69 
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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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    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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    Bulletin of mathematical biology 37 (1975), S. 71-78 
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    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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    Bulletin of mathematical biology 37 (1975), S. 127-138 
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    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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    Bulletin of mathematical biology 37 (1975), S. 565-572 
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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 
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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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    Bulletin of mathematical biology 37 (1975), S. 573-588 
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    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 
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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 
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    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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    Bulletin of mathematical biology 37 (1975), S. 419-425 
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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 
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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 
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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 
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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 
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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 38 (1976), S. 205-207 
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    Bulletin of mathematical biology 38 (1976), S. 161-192 
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    Notes: Abstract In order to evaluate the effect of anatomic asymmetries on the gas concentration distribution in the pulmonary airways, a Monte Carlo simulation of combined bulk flow and molecular diffusion was carried out in a realistic distal airway model (Parkeret al., 1971). This airway model, composed of branches distal to the 0.5-ram diameter airways, contained an upper symmetric segment consisting of four generations of conducting airways and a lower asymmetric segment of alveolar ducts and sacs arranged in five transport paths of varying lengths. In accounting for the volume increases of these ducts and sacs occurring during normal respiration, uniform alveolar filling rates and a fixed length-to-diameter ratio of all airways were assumed. For a pulse injection of inert tracer gas, the simulation was employed to determine the longitudinal concentration profiles in the conducting airways. In the alveolated airways, not only were the longitudinal profiles determined along each path, but radial transport from the core to the periphery of the airways was considered. The results of the simulations indicate that geometric asymmetries alone contribute substantially to regional concentration variations in the distal airways. For example, when a gas bolus is injected at mid*inspiration, there are concentration differences as great as 40% between two points along different transport paths located equi-distant from the proximal end of the model. As viewed from the terminal end of the model (acinus), average concentration differences as large as 6-to-1 exist between the longest and shortest transport paths respectively for gas boli introduced near the end of inspiration. The results further indicate because of large radial diffusion rates, no significant concentration differences exist between the periphery a-ld the central core of alveolated airways. Simulation of the expired concentration profiles indicate that boll injected very late during inspiration exhibit a sloping tail, unlike the earlier injected boll whose tails are virtually horizontal. Through the use of superposition teehniqnes, it was found that these sloping tails correspond to an alveolar slope of 1.5 vol% between 750 and 1250 ml expired for a continuous washing of tracer. This result is in disagreement with other transport analyses which did not directly account for the effect of geometric asymmetries.
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    Notes: Abstract Assuming a spherical geometry for the left ventricle, passive elastic stiffness-stress relations have been obtained on the basis of linear elasticity theory and large deformation theory. Employing pressure-volume aata taken from rat hearts of various age groups, it is shown that young rat heart muscle (1 month) is stiffer than either adult (7 months) or old rat heart muscle (17 months). Although the qualitative results are similar for both elasticity theories, the large deformation theory gave results in closer agreement with those obtained from papillary muscle studies. These results imply that stiffness of muscleper se can be assessed from left ventricular pressure-volume data.
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    Bulletin of mathematical biology 38 (1976), S. 277-293 
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    Notes: Abstract Deliberate evaluation of the quantum theory of nerve excitation is made by comparing it with Hill's theory in fitting the experimental data on threshold-frequency relation, optimum frequency (v0) for nerve excitation and strength-duration relation. Decrease of v0 and increase of all the time constants (Hill's λ andk, Wei'sT 2 and spike durationw) with decreasing temperature are interpreted on the basis of the dipole relaxation timeT 2 but inexplicable from Hill's theory or any other existing theory. The closeness ofk,T 2 andw values is explained. A variety of experimental results obtained by others is discussed. Finally, a comparison is made between the Hodgkin-Huxley equations and the quantum theory. Most of the facts (electrical and non-electrical) tend to support the thesis that nerve excitation is a macroscopic expression of quantum transitions of dipoles between energy states.
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    Bulletin of mathematical biology 38 (1976), S. 317-319 
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    Notes: Abstract In the periodic Leslie model the asymptotic period of total population is a divisor of the asymptotic period of the population vector. Under reasonable circumstances these periods are identical.
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    Bulletin of mathematical biology 38 (1976), S. 305-315 
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    Notes: Abstract A number of biological branching systems, such as the bronchial and pulmonary arterial trees, are being investigated in an ongoing study in order to define their physiological properties. The technique involves the description of branching trees by the use of hierarchical systems of ordering, especially those described by Horsfield and by Strahler. During this work some mathematical properties of branching trees were demonstrated and these are described in this paper.
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    Bulletin of mathematical biology 38 (1976), S. 323-324 
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    Bulletin of mathematical biology 38 (1976), S. 209-217 
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    Bulletin of mathematical biology 38 (1976), S. 387-400 
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    Notes: Abstract Luteinizing hormone (LH) is secreted continuously from the anterior pituitary gland. The concentration in the blood of this gonadotropic hormone plays a regulatory role in the development of puberty in both sexes, in the induction of ovulation in females, and in the production of testosterone in males. The secretion of LH is in turn controlled by luteinizing hormone releasing hormone (LHRH) secreted by the hypothalamus. LH and LHRH are removed from the blood by degradation and excretion. This hormonal system is modelled by a system of ordinary differential equations based upon specific physiological and biochemical assumptions current among experimentalists in this field. The one exception is the assumption that LHRH may bind reversibly to a serum protein; an analysis of the data shows that this or a similar mechanism is a crucial specification. Data on the serum levels of LH and LHRH in two human subjects were fitted using the model. The data consist of the transients and subsequent decays created by a bolus intravenous injection of LHRH.
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    Bulletin of mathematical biology 38 (1976), S. 401-413 
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    Notes: Abstract A thick-wall incompressible, elastic sphere was used as a model for the diastolic rat left ventricle. A model for myocardial nonhomogeneity was derived assuming that fiber (circumferential) stress was independent of position in the ventricular wall. The theoretical implications of the resulting constitutive relations together with the spherical model were analyzed in the context of large deformation elasticity theory. It was found that muscle stiffness at a given level of uniaxial stress increased monotonically from the endocardium to the epicardium. In addition, fiber stress was found to be essentially a linear function of transmural pressure above a pressure of 6 g/cm2. It was also shown theoretically that neglecting the nonhomogeneity of the myocardium resulted in a state of stress which differed significantly from that predicted by the nonhomogeneous model. For example, at a transmural pressure of 14 g/cm2, fiber stress in the nonhomogenous model was equal to 17 g/cm2 while fiber stress in the homogeneous model varied between 100 g/cm2 at the endocardial surface and 2 g/cm2 at the epicardial surface. The change in muscle stiffness with position which characterized the nonhomogeneous model also tended to linearize the highly curvilinear radial stress distribution predicted by the homogeneous model at a given transmural pressure.
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    Bulletin of mathematical biology 38 (1976), S. 435-444 
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    Notes: Abstract The phenomenon of axonal transport has been well documented (Ochs, 971; Lasek, 1970; and Grafstein, 1967). In a previous paper, we showed how diffusion alone could not account for this process. In this report we show that convection or convection with diffusion can account for the observed build-up of material. By including a first-order catabolic sequestration term, we are able to offer an understanding of the several apparent rates of transport with the same underlying velocity and variable sequestration.
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    Bulletin of mathematical biology 38 (1976), S. 459-465 
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    Notes: Abstract It is known that the Lotka-Volterra coupled nonlinear differential equations for a two-species prey-predator ecosystem possess a periodic solution, although its exact form is not yet obtained analytically. The conventional linearization approximation for solving these nonlinear equations leads to a harmonic oscillator whose frequency depends only on the intraspecific coefficients. We propose here a prescription for obtaining nonlinear correction to the linear frequency by using the Hamilton-Jacobi canonical formalism of classical mechanics. It is found that the first-order correction, which also involves interspecific parameters, exhibits the basic qualitative features of the nonlinearity.
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    Bulletin of mathematical biology 38 (1976), S. 467-478 
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    Notes: Abstract Environmental safety testing typically requires procedures for extrapolating from the relatively high experimental to the very low use doses of potentially harmful substances. In the present paper, a stochastic mammillary compartmental model for environmental safety testing is proposed and extrapolation procedures based on its dose-response relationship are developed. The proposed model is a direct generalization of one of the basic safety models, the one-hit model, in that a harmful reaction is assumed to occur if at any time any of the peripheral compartments attains a specified threshold of particles. Consideration of a closed model yields an upper bound on the probability of attaining a certain threshold level, thus providing a conservative procedure for extrapolating to a low dose, while a lower bound obtained from a related open model provides a useful monitoring device as to the sharpness of the upper, bound. The extrapolation procedure is illustrated with simulated data and approximations for initial values are developed.
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    Bulletin of mathematical biology 38 (1976), S. 505-516 
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    Notes: Abstract By using chromosome images as a framework, algorithms for finding most dissimilar images are presented and illustrated by examples. In terms of angles, a chromosome image consists of two exterior biangles and two interior biangles. Biangles are defined and classified into 180° biangles, 〉180° biangles and 〈180° biangles. The dissimilarity of biangles and its geometric interpretation together with various properties of biangles are also presented. The results may have useful applications in pattern recognition, scene analysis, information storage and retrieval, artificial intelligence and fuzzy set theory.
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    Bulletin of mathematical biology 38 (1976), S. 517-526 
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    Notes: Abstract The Volterra equations which represent competitions between two species are utilized to examine the phenomenon of boundary formation between two species of plants. The set of stable stationary points for these equations is determined and is illustrated in a product space of parameters and dynamical variables. The stages of boundary appearance and succession are visualized by considering slow changes of the parameters as functions of time and space.
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    Bulletin of mathematical biology 40 (1978), S. 45-58 
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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 
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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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    The Geneva risk and insurance review 10 (1978), S. 50-66 
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    Topics: Economics
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    The Geneva risk and insurance review 10 (1978), S. 44-49 
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    Topics: Economics
    Notes: Conclusion For all these reasons, the rediscovery of the equivalence theorem, first stated by David Ricardo in 1817, must be rejected as an adequate basis for policy, just as Ricardo had denied its applicability to the real world. Correspondingly, the concern with the adverse consequences of unfunded social insurance wealth for the supply of national saving, capital intensity, and living standards remains well founded. p ]If, as a practical matter, public pension and social security programs will never be funded actuarially in the United States and most other postindustrial countries, then government-supervised substitution of private for public retirement plans is the only way to achieve at least partial funding. If such substitution follows the British model of allowing employers to contract out of the earnings-related part of the state scheme if equivalent pensions are provided by the company plan, payroll taxes and social security wealth decline so as to reduce their adverse impact on capital formation.
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    The Geneva risk and insurance review 10 (1978), S. 73-84 
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    The Geneva risk and insurance review 10 (1978), S. 85-95 
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    The Geneva risk and insurance review 10 (1978), S. 96-98 
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    The Geneva risk and insurance review 11 (1979), S. 5-13 
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    The Geneva risk and insurance review 10 (1978), S. 67-72 
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    Notes: Summary: Social Policy in the Italian Economy Favourable social and economic conditions constitute the essential framework for a stable development of savings. Saving in the form of insurance becomes advantageous for the individual, and private insurance can thus extend its activity, when social attitudes and the economic situation favour the propensity to save. If conditions change, the State can take over the coverage of risks through social insurance. By means of this institutions, an anti-cyclical policy can be pursued: the amount of social security contributions, for instance, can be increased during the expansion of the cycle and the amounts thus accumulated can be used to grant benefits during the recession period, when contributions can be fixed at a lower percentage of wages. Another type of policy can be pursued by government authorities: that of adjusting social security contributions to industrial profits, thereby directing the subsequent effects on economic growth. Inflation cab cause instability in decisional policies taken by private insurance companies. A solution to the unbalanced increase of costs can be found in index-linking. Life policies of this kind, for instance, cab be closely related to investments in houses, to be bought by the insured themselves in price-linked instalments. After a reference to present developments regarding risk instability and to possibilities of new forms of insurance, this paper considers the competition resulting from the opening of the EEC insurance markets as an opportunity for the Italian market to strengthen its structures.
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    Bulletin of mathematical biology 39 (1977), S. 663-678 
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    Notes: Abstract A number of apparently different lines of inquiry into fundamental biological processes point to the central role played by the notion of observation in the theory of biological systems. Not only do we use the results of our own observations to obtain the system descriptions which are the starting-points for an understanding of biological processes, but it is a basic postulate of physics that the interactions between biological systems themselves can be regarded as observations. On this basis, it is clear that we cannot properly understand biological interactions unless the observables we employ for system description are the same as those involved in the interactions we are describing. To do this requires a general theory of observables and system description, establishing the relationship between different modes of description. A sketch of such a theory is developed in the present paper, using only two postulates: (a) that all interactions are determined by the values of observables of a system evaluated on specific states, and (b) that real-valued observables suffice. As an application, a specific test is proposed whereby it can be determined whether the observables employed to describe interacting systems are sufficient to specify the observables involved in the interaction itself.
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    Bulletin of mathematical biology 39 (1977), S. 679-691 
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    Notes: Abstract Differential equations are derived whose solution gives the cross-sectional shape of a flexible tube as a function of the transmural pressure. These equations are solved digitally to produce a series of closed curves, each curve representing the shape of a cross section for a particular set of conditions. These are then applied to the case of systemic arteries, pulmonary arteries, and large veins. The results predict that systemic arteries must always be circular, even when the internal and external pressures are equal. In veins, a small positive internal pressure causes them to become circular, regardless of their initial state, with negligible stretching. Further increases in internal pressure cause the area of the cross section to increase due only to stretching, the shape remaining essentially circular. With pulmonary arteries, known to be noncircular, changes in the cross-sectional area result from a combination of stretching and changes of shape.
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    Bulletin of mathematical biology 39 (1977), S. 693-704 
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    Notes: Abstract Stochastic models of human reproduction are beginning to play significant roles in the evaluation of family planning programs. A class of stochastic processes called absorbing, agedependent, semi-Markov processes frequently arises in the construction of such models. The paper begins with a discussion of some technicalities regarding absorbing, age-dependent, semi-Markov processes. Then, an algorithm due to Littman, which makes possible the computerization of this class of stochastic processes, is presented. Briefly, Littman’s algorithm provides an efficient method for numerically solving systems of renewal type integral equations, provided the system does not contain a large number of equations. After setting down a concrete model for a large clinical trial of intrauterine devices conducted in Taiwan, the paper concludes with a discussion of a method for validating the model based on the data collected in the clinical trial.
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    Bulletin of mathematical biology 39 (1977), S. 743-743 
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    Bulletin of mathematical biology 39 (1977), S. 705-719 
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    Notes: Abstract Some theoretical requirements for the valid use of hemolytic plaque inhibition as a method for studying cellular selection and recognition in an immune response are reviewed. Aside from providing a rational basis for the use of this technique, the theory resolves a growing body of apparently conflicting results on the affinity regulation of IgM secreting cells and can also be used to deduce structural (in particular, morphological) features of the IgM molecule. The diverse predictions of the theory are examined in light of experimental results and find support in a wide data base. Additional specific experiments are proposed which can be used in conjunction with the theory to help clarify the relation between cellular proliferation and maturation.
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    Bulletin of mathematical biology 39 (1977), S. 721-741 
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    Notes: Abstract A theory of the cell volume is presented with emphasis on the swelling effect of high concentrations of KCl and other chloride salts. In this theory a particular cell volume represents a state of balance between the tendency of the cell water to build deeper layers of polarized water and the restraining forces exerted by the salt linkages and H-bonds. Taking into account also the different structure-breaking effects of different salts, theoretical curves can be constructed which describe the complex multiple peak-plateau of swelling curve observed in frog muscle in response to increasing concentrations of different chloride salts.
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    Bulletin of mathematical biology 22 (1960), S. 391-415 
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    Notes: Abstract Some progress has been made on the problem of the interaction of respiratory gases with whole blood. A practical working model for oxygen absorption in and interaction with whole blood is developed by assuming that oxygen molecules compete with protons for binding sites on the hemoglobin molecule and by invoking the Wyman-Allen (Jour. of Polymer Science,5, 499–518, 1951) hypothesis that two oxygen molecules go on the hemoglobin at one time. Extensive tests of this model against saturation measurements on blood from humans, horses, oxen and sheep are made. Values for the equilibrium constants are calculated and compared. In addition a second working model has been developed in an attempt to explain why O2 saturation measurements when expressed as (100 percent — percent saturation) are an exponential function of oxygen partial pressure. Considerations which make plausible the following expression for saturation, [1−2e −γx/h1/2/(1+(1/20)(β′/h 1/2+h 1/2/β′))] are presented. Herex denotes oxygen tension,h denotes hydrogen ion concentration and β′ and γ are parameters.
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    Bulletin of mathematical biology 23 (1961), S. 1-14 
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    Notes: Abstract Some progress has been made on the problem of the interaction of respiratory gases with whole blood. A working mathematical model for the O2−CO2 interaction phenomena has been developed from mathematical studies of the data. The Edsall-Wyman (1958) model for CO2 absorption is improved upon in this paper by consolidating it with the O2 absorption model developed in paper I of this set (Bernard, S. R.,Bull. Math. Biophysics,22, 391–415, 1960). This improved model assumed the effect of O2 on CO2 absorption is mediated through the electrical charge possessed by the hemoglobin molecule,i.e., O2 molecules bound to hemoglobin displace protons from the hemoglobin thereby increasing the negative charge on the hemoglobin and at the same time increasing the acidity of the solution. The model is tested against the data.
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    Bulletin of mathematical biology 23 (1961), S. 15-18 
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    Notes: Abstract On the basis of previously proposed mathematical models of social behavior, the present note investigates the possibility of the control of behavior remaining permanently in the hands of one class, if this class possesses sufficient means for influencing mass behavior. The conclusion is reached that, with the assumptions made, if the behavior imposed by the controlling class leads to sufficiently strong dissatisfaction, the control will pass to another class, no matter how strong the controlling power of the first.
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    Bulletin of mathematical biology 23 (1961), S. 19-29 
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    Notes: Abstract Traffic in one direction on a multilane highway is considered, and a general expression for the number of cars which pass a car travelling at a given velocity, as well as the number of cars which the given car passes, is derived for the case when the speeds of different cars are distributed in some arbitrary manner. Closed expressions are derived and discussed for a rectangular distribution. Each passing by another car or of another car is considered as a distracting stimulus which affects the reaction times of the driver. Using previously derived expressions for the safe speed as a function of reaction times, expressions for the safe average speed are derived, in terms of the volume of traffic and of the spread of the distribution of speeds.
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    Bulletin of mathematical biology 23 (1961), S. 99-103 
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    Notes: Abstract Emphasis upon the importance of homeostatic feedback has drawn attention away from the complexity of biological processes. A study of glucose metabolism indicates the importance of open-cycle as well as closed-cycle mechanisms. Besides the glucose-dependent mechanism of insulin secretion, many open-cycle processes involving the liver, adrenal glands and kidneys, play important roles in the variation of blood glucose. In addition, glucose utilization by the tissues is essentially open-cycle in nature.
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    Bulletin of mathematical biology 23 (1961), S. 105-106 
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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 23 (1961), S. 413-416 
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    Notes: Abstract In certain situations like the aftermath of a revolution when discontent rises amongst certain groups of the population, it is frequently observed that the discontented groups are firmly convinced that their point of view is shared by the majority of the population. Yet future events prove that this is far from being the case. This effect is partly attributable to “wishful thinking,” partly to a purely social mechanism. The wishful-thinking effect may be considered as a case of psycho-physical discrimination in which a bias is introduced proportional to the degree of satisfaction anticipated from a given situation. H. D. Landahl's well-known equations can be applied to this case. The social factor is based on the circumstance that an individual associates by preference with such other individuals as have similar opinions. This results in an actual error of estimation of the relative minority or majority because of different frequencies of contact with individuals of the two opposing groups. Both factors may be combined into one equation.
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    Bulletin of mathematical biology 23 (1961), S. 421-422 
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    Bulletin of mathematical biology 25 (1963), S. 367-385 
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    Notes: Abstract In Part II we prove some of the more complicated theorems stated and used in Part I. In particular, we derive the distribution functionsD 1,D 2, andD 3, and prove some of their properties under various limiting conditions.
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    Bulletin of mathematical biology 25 (1963), S. 387-392 
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    Notes: Abstract The graphical treatment utilized by Marmasse in order to test “Wurmser’s theory of agglutination” has been applied, taking into account all the data available. Contrary to Marmasse’s conclusion, the application of this graphical method is not a valid argument against the theory.
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    Bulletin of mathematical biology 25 (1963), S. 343-366 
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    Notes: Abstract This is the continuation of part I, which was published in the September, 1963, issue ofThe Bulletin. Section 5 treats the special case in which the left absorbing barrier recedes to −∞, leaving essentially only one barrier at a finite distance Λ (〉0) from the origin. The eigenfunctions are now parabolic cylinder functions. The limiting cases Λ→+∞ and Λ→0 are also considered. Though meaningless for practical applications to our problem, they are of interest, mathematically, because the Green’s function for the solution of the Fokker-Planck equation assumes a particularly simple form. In section 6 we study, by means of an example, how the “force of mortality” may vary with time before attaining its final asymptotic value. Section7, still dealing with only one absorbing barrier, shows that our results for “strong homeostasis” are identical with those derived by Chandrasekhar for the escape of particles through a potential barrier in the limiting case of quasi-static flow. Precise conditions are given for the validity of both the quasi-static and the Smoluchowski approximations to the Fokker-Planck equation. Finally, in section 8, a brief mention is made of Gevrey’s method for the solution of parabolic partial differential equations.
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    Bulletin of mathematical biology 25 (1963), S. 393-419 
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    Notes: Abstract The derivation of learning models relative to choice behavior in experimenter-subject controlled experiments with two outcomes (right or wrong) is considered from the point of view that any such model must satisfy a criterion of optimality. The criterion adopted for investigation, termed optimal asymptotic behavior, is that of the subject asymptotically learning which of the alternatives has the greater probability of being correct. A class of path-dependent linear models is posed as possible candidates. It is shown that no members of this class satisfy the criterion although two of them approach it by making a learning parameter small enough. The possible implications of this are discussed.
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    Bulletin of mathematical biology 26 (1964), S. 25-29 
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    Notes: Abstract Error-detecting codes have been known to mathematicians and to electrical engineers for over ten years. In general, such codes utilize an additional orparity bit for purposes of detecting errors by the addition of all positive binary bits or “1’s” occurring in any code word. However, since the process of addition is required for such code detection, it is not surprising that these codes have not been applied to the nucleic acid molecule. In 1962, P. I. Hershberg (Trans. I.R.E., CS-10, 280–4, 1962) outlined a categorical constraint which permitted the realization of a class of error-detecting codes which did not require parity bits. This class of codes is applied to the nucleic acid molecule in the present paper.
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    Bulletin of mathematical biology 26 (1964), S. 31-38 
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    Notes: Abstract Compartment systems are often used as models for tracer and drug kinetics. The structure of a compartment system is here analyzed by means of theory of graphs methods. In particular the precursor-successor relationship between any two compartments is classified according to the structure of the graph of the system and to the values of the elements of the matrix associated with it.
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    Bulletin of mathematical biology 26 (1964), S. 39-43 
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    Notes: Abstract An application of a bifurcation theorem shows the existence of periodic solutions of a system of differential equation used to describe competition between two species. It is then shown that the results are more general than those previously established.
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    Bulletin of mathematical biology 26 (1964), S. 9-24 
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    Notes: Abstract The 2o and 10o field color-matching functions are independent: one specification is not a linear transformation of the other, even after correcting for macular pigment effects. Therefore, the “true” color-matching functions which directly describe the linear responses of the eye must be different for the two field sizes. This means that a given stimulus will, in general, have a different chromaticity depending upon the field size, regardless of the choice of any one colorimetric co-ordinate system for all field sizes. However, in spite of these chromaticity differences, a large uniform field usually appears nearly uniform. Such color uniformity implies that even though chromatic differences occur as a function of retinal position or field size, these differences are small. If this is the case, then the underling “true” color-matching functions determining the observed color-matching functions must be nearly, but not quite, identical. These differences vanish as identity between the sets of color-matching functions is approached. This property suggests a method of calculating the “true” color-matching functions. The “true” color-matching functions must approximate those obtained by minimizing the chromaticity differences between two independent sets of data. This can be done by assuming that the coefficients of transformation should be adjusted so as to produce as nearly identical chromaticities for spectrum stimuli as possible. In this paper, it is also assumed that the “true” color-matching functions have no negative values, as if they were based on actual absorption spectra. This article describes the calculation of the “true” 2o and 10o field color-matching functions satisfying these two conditions. For both field sizes, the maxima of the three functions are near 435, 540, and 585 mμ, after correcting for the filtering effects of the ocular media and macular pigment.
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    Bulletin of mathematical biology 26 (1964), S. 45-47 
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    Notes: Abstract In this note the principal convergence theorem (F. Rosenblatt,Principles of Neurodynamics, Spartan Books, Washington D.C., 1962, 111–116) is proved by a new method.
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    Bulletin of mathematical biology 26 (1964), S. 49-55 
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    Notes: Abstract Considering only nearest neighbor interactions, an expression is obtained for the grand partition function for the adsorption of two kinds of monovalent positive ions at a long chain of one type of monovalent negative fixed sites in an electric field. Expressions are obtained for the fractions of sites which are occupied by each kind of ion as well as of those which are unoccupied as a function of the potential of the electric field.
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    Bulletin of mathematical biology 26 (1964), S. 57-61 
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    Notes: Abstract In connection with a series of previous papers by this author (Bulletin of Mathematical Biophysics,21, 299–308, 375–385;22, 257–262, 263–267;23, 19–29;24, 319–325) results obtained by A. Crawford (Economics 5, 417–428) on the effects of irrelevant lights on reaction times toward a given light stimulus are discussed. The conclusions from a previous paper of this author (Bulletin of Mathematical Biophysics,23, 19–29) are elaborated.
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    Bulletin of mathematical biology 26 (1964), S. 77-81 
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    Notes: Abstract A mathematical model has been constructed to describe experimental data recorded in a study of a simple avoidance situation. The theoretical description makes use of the concept of the effective number of shocks. The model explains the existence of oscillations encountered in previous experiments.
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    Bulletin of mathematical biology 26 (1964), S. 63-75 
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    Notes: Abstract Response probabilities are interpreted from two points of view. One corresponds to fluctuations in physical parameters suggestive of a neurological basis, and the other corresponds to fluctuations in stimulus sample constitution. The two interpretations are shown to be equivalent under rather general conditions, giving the same type of relation between response and training states. This relation is different from that obtained via the response strength concept used in Part I. As a step toward evaluating the difference in predicted behavior for these different response-training relations, a general functional-difference equation is derived that describes the moments of the corresponding stochastic process in experimenter-subject controlled experiments. As an immediate application, it is used to obtain the continuity condition for the solution of the functional equation treated in Part I, and to justify the differentiability conditions assumed in establishing asymptotic properties of the solution as a function of the reinforcement parameter.
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    Bulletin of mathematical biology 26 (1964), S. 83-89 
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    Notes: Abstract A simple avoidance situation is considered in terms of a neural net learning model. Data for the control situation can be represented by an expression having three parameters which determine the initial and the steady state activities together with the transient aspects. The introduction of a learning parameter then allows one to calculate satisfactorily the results obtained in the experimental situation in which shock is applied.
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    Bulletin of mathematical biology 26 (1964), S. 101-101 
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    Bulletin of mathematical biology 26 (1964), S. 91-100 
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    Notes: Abstract An algebraic representation of operations of genetic recombinations is illustrated. It is shown that the recombinations between chromosomes in the two-strand model can be represented by groups, in the sense of the theory of groups. Recombinations between chromosomes with inversions and a translocation are considered as well as cases without them. It is found that the groups derived from such cases are Abelianp-groups (p=2) and that the types of the Abelian groups for the various pairs of chromosomes are different from each other. Differences among those recombination groups are illustrated by showing the sets of generators of the various groups, which generate the corresponding recombination groups by multiplication.
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    Bulletin of mathematical biology 26 (1964), S. 103-111 
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    Notes: Abstract It is shown that a rather close relationship exists between the (ℳ,ℛ)-systems, defined previously as prototypes of abstract biological systems, and the sequential machines which have been studied by various authors. The theory of sequential machines is reformulated in a way suitable for its application to the study of the intertransformability of (ℳ,ℛ)-systems as a result of environmental alteration. The important concept of strong connectedness is most useful in this direction, and is used to derive a number of results on intertransformability. Some suggestions are made for further studies along these lines.
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    Bulletin of mathematical biology 26 (1964), S. 113-120 
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    Notes: Abstract Blood flows into the aorta and its branches during left ventricular systole. Most of the arterial walls in the body stretch during systole in accordance with their elastic properties (Roston, 1962a, b). During diastole, the rebound of the distended walls supplies an additional propulsive force pushing the blood forward. Since the metabolic exchange between most of the tissues in the body and their blood vessels is ordinarily the same throughout the cardiac cycle, it makes little difference whether or not the blood flow occurs during systole or diastole. The circulation in the coronary arteries behaves in a quite different way. Because the muscle fibers of the heart contract during systole and relax during diastole, different conditions for blood flow and metabolic exchange exist during the phases of the cardiac cycle. As a result, specification of whether blood flows in the coronary arteries during systole or diastole may be important. Such specification complicates the study of the coronary artery circulation. For example, because of the arterial elasticity, some of the blood which enters the coronary arteries during diastole comes in contact with the muscle fibers during systole. The present work contains a theoretical study of the coronary artery circulation.
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    Bulletin of mathematical biology 26 (1964), S. 139-146 
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    Notes: Abstract A study is made of the adsorption of one kind of monovalent positive ion at a long chain of alternating monovalent negative fixed charged (“lattice”) and uncharged (“interstitial”) sites both of one type in an electric field. Considering only nearest neighbor interactions an expression is obtained for the grand partition function. The fractions of sites of both types which are occupied and unoccupied are determined. It is shown that an equilibrium constant can be defined for the adsorption of ions at oppositely charged sites.
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    Bulletin of mathematical biology 26 (1964), S. 121-138 
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    Notes: Abstract This paper proposes a model for color perception which accounts for variations in the dimension of the space of perceived colors. The model assumes that there is only one type of cone with only one shape of response curve, but that different cone's response curves differ by translation. It also assumes that the final discrimination system, learned from originally random connections, maximizes discrimination in the normal visual environment. Learning mechanisms are discussed, and the form which the final discrimination system ought to take is plausibly derived. An algorithm for the tristimulus curves is obtained from this model, and it is shown that a good fit of the empirical data can be obtained.
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    Bulletin of mathematical biology 26 (1964), S. 187-191 
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    Notes: Abstract It has been suggested by Robert Rosen (Bull. Math. Biophysics,22, 227–255, 1960) that multiple alleles or pseudoalleles correspond to multiple cites of degenerate states of some quantum mechanical observable which acts as a source of primary genetic information. It is pointed out here that if the quantum mechanical states are determined by the different sequences of the purine and pyrimidine bases in the DNA molecule, the expected number of pseudoalleles would be much too large. The expected number is considerably reduced if we assume that a quantum mechanical state determines the coupling between a molecule of transfer RNA and the corresponding amino acid.
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    Bulletin of mathematical biology 26 (1964), S. 147-166 
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    Notes: Abstract This paper describes a mathematical model developed to simulate the physical characteristics of the human thermal system in the transient state. Physiological parameters, such as local metabolic heat generation rates, local blood flow rates, and rates of sweating, must be specified as input data. Automatic computation of these parameters will be built into the model at a later date when it is used to study thermal regulation in the human. Finite-difference techniques have been used to solve the heat conduction equation on a Control Data Corporation 1604 computer. Since numerical techniques were used, it was possible to include many more factors in this model than in previous ones. The body was divided into 15 geometric regions, which were the head, the thorax, the abdomen, and the proximal, medial, and distal segments of the arms and legs. Axial gradients in a given segment were neglected. In each segment, the large arteries and veins were approximated by an arterial pool and a venous pool which were distributed radially throughout the segment. Accumulation of heat in the blood of the large arteries and veins, and heat transfer from the large arteries and veins to the surrounding tissue were taken into account. The venous streams were collected together at the heart before flowing into the capillaries of the lungs. Each of the segments was subdivided into 15 radial sections, thereby allowing considerable freedom in the assignment of physical properties such as thermal conductivity and rate of blood flow to the capillaries. The program has been carefully checked for errors, and it is now being used to analyze some problems of current interest.
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    Bulletin of mathematical biology 26 (1964), S. 193-198 
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    Notes: Abstract A model is introduced in which the reabsorption of sodium is governed by an enzymatic process. This process is in turn assumed to be influenced by the extracellular volume which depends on the amount of sodium in the body at a given time. The model allows for damped oscillations when the sodium intake lies within range of values and thus can account for observed oscillations.
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    Bulletin of mathematical biology 26 (1964), S. 167-185 
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    Notes: Abstract A neurobiophysical model is proposed for the explanation of some characteristics of schizophrenic behavior. The normal reactions to exogenous stimuli are mediated through a set of centers, while some endogenous stimuli result in abnormal reactions removed from reality, such as dreamlike states, paranoias, hallucinations, etc. The two sets of centers are cross-inhibited and the usual equations for such cross-inhibited systems are applied. In normal life exogenous stimuli as a rule result preponderantly in pleasant reactions, and the corresponding pathways are therefore reinforced. This results in an inhibition of the abnormal reactions. If the life history of an individual is such that a sufficiently large number of ordinarily experienced stimuli leads to unpleasant reactions and, therefore, the corresponding pathways are inhibited, the endogenously stimulated centers for abnormal reactions prevail and various schizophrenic symptoms occur. The same result may be achieved with a normal life history but through organic changes in the system, which differentially affect various thresholds and excitation parameters. The model thus leads to the conclusion that what appears now to be a large array of contradictory findings in the “organic” versus the “psychological” controversy is actually not a contradiction, but is a result of the dependence of normal and abnormal behaviors on a large number of neurobiophysical parameters. Some general comparisons between the conclusions drawn from the model and some known facts are made. The model also provides a first step toward a neurobiophysical interpretation of the mechanism of psychotherapy.
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