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  • Articles  (39,391)
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  • Articles  (39,391)
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  • 1
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    Bulletin of mathematical biology 33 (1971), S. 49-54 
    ISSN: 1522-9602
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract In the theory of organismic sets (Bull. Math. Biophysics,31, 159–198, 1969) we considered organisms as sets endowed with certain “activities,” the latter’s resulting in a set of “products.” Those products may be of a material nature, like a hormone secreted by a cell, or of a non-material nature, like a feeling or an attitude. In the present paper aggressiveness and submissiveness are considered as such non-material products of the activities of the brain cells. A general description of aggressiveness and submissiveness is given in terms of organismic sets. Cycles in “peck order” are thus naturally explained.
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  • 2
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    Bulletin of mathematical biology 33 (1971), S. 55-66 
    ISSN: 1522-9602
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    Notes: Abstract In line with previous studies on organismic sets, the division of all organismic sets intogeneral autotrophic and heterotrophic is introduced. The first produce their food themselves from some external source of energy, which in general may be an energy of any kind. The others use other organismic sets as the source of their food and energy. On earth we know only one kind of generalgeneral autotrophic organismic sets, namely, the autotrophic plants which use solar radiation as their source of energy and for production of their own food. It is shown why autotrophic animals do not exist on earth except as microorganisms like, e.g.,Euglena. A rigorous proof of the previously derived theorem that in an organismic set of ordern〉1 no element can be completely specialized is given. It requires the introduction of new postulates. Finally, in considering the organic world as a whole, the notion of organismic sets ofmixed order is introduced.
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  • 3
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    Bulletin of mathematical biology 33 (1971), S. 67-81 
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    Notes: Abstract It appears to be axiomatic that termolecular and higher order reactions occur relatively rarely. The basis for this judgment seems to lie in the supposition that successful 3-Body collisions of 3 interactive species of molecules cannot occur frequently enought to account for chemical or biochemical transformation. In order to provide a more complete mathematical framework than now exists for examining this hypothesis the probability of effective termolecular “δ-collisions” as a function of time is derived. This amounts to adding to the class of reactions for which stochastic models are now available the termolecular reaction. In common with the unimolecular and bimolecular cases this process is seen to satisfy the criterion of consistency-in-the-mean with respect to deterministic formulations. It is planned next to use the termolecular process and the lower order processes in computer-assistedin numero experimental studies aimed at comparing alternative mechanisms of reaction.
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  • 4
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    Bulletin of mathematical biology 33 (1971), S. 83-96 
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    Notes: Abstract Small sample properties of the maximum likelihood estimator for the rate constant of a stochastic first order reaction are investigated. The approximate bias and variance of the maximum likelihood estimator are derived and tabulated. If observations of the system are made at timesiτ,i=1, 2, ...,N; τ〉0, the observational spacing τ which minimizes the approximate variance of the maximum likelihood estimator is found. The non-applicability of large sample theory to confidence interval derivation is demonstrated by examination of the relative likelihood. Bartlett’s method is employed to derive approximate confidence limits, and is illustrated by using simulated kinetic runs.
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  • 5
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    Bulletin of mathematical biology 33 (1971), S. 339-354 
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    Notes: Abstract The representation of biological systems by means of organismic supercategories, developed in previous papers (Bull. Math. Biophysics,30, 625–636;31, 59–71;32, 539–561), is further discussed. The different approaches to relational biology, developed by Rashevsky, Rosen and by Băianu and Marinescu, are compared with Qualitative Dynamics of Systems which was initiated by Henri Poincaré (1881). On the basis of this comparison some concrete result concerning dynamics of genetic system, development, fertilization, regeneration, analogies, and oncogenesis are derived.
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  • 6
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    Bulletin of mathematical biology 33 (1971), S. 303-319 
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    Notes: Abstract Some years ago (Rosen 1958a, b; 1959) we described a class of metaphorical, relational paradigms for cellular activity which we termed (M, R)-systems. A sizable amount of subsequent work, to be itemized below, has been devoted to an exploration of some of the properties of these systems. The main purpose of the present paper is to put this class of paradigms into a general system-theoretic perspective, with a particular view to appraising the relation between the type of system description embodied in the (M, R)-system and other kinds of physical and mathematical descriptions of cellular systems. Thus, the principal aim is to establish the relationships and connections between the global relational formalism embodied in the (M, R)-systems and the empirical descriptions which still represent the bulk of our biological knowledge.
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  • 7
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    Bulletin of mathematical biology 33 (1971), S. 321-338 
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    Notes: Abstract After giving a brief review of the theory of organismic sets (Bull. Math. Biophysics,29, 139–152, 1967;31, 159–198, 1969), in which the concept of relational forces, introduced earlier (Bull. Math. Biophysics,28, 283–308, 1966a) plays a fundamental role, the author discusses examples of possible different structures produced by relational forces. For biological organisms the different structures found theoretically are in general agreement with observation. For societies, which are also organismic sets as discussed in the above references, the structures can be described only in an abstract space, the nature of which is discussed. Different isomorphisms between anatomical structures, as described in ordinary Euclidean space, and the sociological structures described in an abstract space are noted, as should be expected from the theory of organismic sets.
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  • 8
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    Notes: Abstract Current psychological research into the inference (diagnostic) process is briefly reviewed, using as a vehicle an investigation of the prediction of the probability of success of hypothetical applicants to a graduate program in biology. Brunswik’s lens model and multiple regression analysis are used, as is a Bayesian approach. Four judges’ (biologists’) predictions are analyzed. Some general conclusions about inference, drawn from the current data in psychology, are presented.
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  • 9
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    Bulletin of mathematical biology 33 (1971), S. 451-462 
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    Notes: Abstract A mathematical model has been developed to simulate the glucose-insulin interaction following a glucose load such as occurs in an IVGTT. This model differs from earlier models in that the insulin response to glucose loading is a recurring all or none threshold response. The model has been simulated on a digital computer using the digital analog simulation language CSMP.
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  • 10
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    Bulletin of mathematical biology 33 (1971), S. 463-479 
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    Notes: Abstract The composite nature of bone dictates the use of a model for bone which is transversely isotropic. We solve the associated sets of partial differential equations governing the dynamic elastic behavoor of a two-layered cylindrical-shaped bone. The solution is analyzed for long, short, and intermediate length waves. The special case of compact bone is treated for long and short wave lengths and a numerical example is worked out to determine the wave speeds (for short wave lengths) given a set of elastic constants, determined by ultrasonic methods, and the bone density, wave frequency, and radius.
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  • 11
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    Bulletin of mathematical biology 33 (1971), S. 481-481 
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  • 12
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    Bulletin of mathematical biology 34 (1972), S. i 
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  • 13
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    Bulletin of mathematical biology 34 (1972), S. 53-63 
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    Notes: Abstract A stochastic model is developed for a compartment with a single time-dependent input, and generalized to include inputs from several sources. With the number of particles of a given molecular species in the compartment as the random variable, the mean, variance and third central moment of this variable are calculated from its generating function, and compared with previous results. The behavior of the calculated moments is discussed, and the possibility of applying the model to chemical and biological systems is considered.
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  • 14
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    Bulletin of mathematical biology 34 (1972), S. 439-441 
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    Topics: Biology , Mathematics
    Notes: Abstract It is shown that from the definition of organismic sets (Rashevsky,Organismic Sets. Some Reflections on the Nature of Life and Society, Holland, Michigan, Mathematical Biology, Inc. and Grosse Pointe, Michigan, J. M. Richards Laboratory) a complete sensory deprivation of an organismic set of ordern=2 should result in malfunctioning of the set. A generalization to higher order sets is suggested.
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  • 15
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    Bulletin of mathematical biology 34 (1972), S. 431-438 
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    Notes: Abstract Optimality in branching structure of the vascular tree was studied. Analysis on its physiological roles as the duct system for blood supply to the capillaries predicted that the vascular tree should be constructed with minimum volume under restriction of determinant pressure, flow and location at the origin and the terminals. Mathematical derivations of this conditional extremum problem yielded some equations expressing the relations between the radii of the branches and their branching angles, which provided numerical solutions for branching points of bi- and poli-terminal minimum volume trees. Comparison of the peritoneal vascular tree in a dog with the minimum volume one computed under the same restrictive conditions showed good agreement in their branching structure.
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  • 16
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    Bulletin of mathematical biology 34 (1972), S. 443-456 
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    Notes: Abstract In order to determine the kinetics of passage of a substance through an organ containing a tangle of vessels, we study the response of a tube to various inflows (perfusion, brief injection, ...). The introduction of the catabolic terms and of the spatial dependence between bulk concentration and surface concentration allows one to account for the difference of arteriovenous concentrations observed experimentally for many metabolites. The relationships between the physico-chemical parameters of the organ and the operational parameters of the model demonstrate the importance of the transit time through the considered vessels. If one considers the different pathways as independent, the introduction of the transit time distribution for an inert substance enables one to compute the response of the organ analytically or by recurrence, using convolution. The parameters of the model can be obtained by the moments method.
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  • 17
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    Bulletin of mathematical biology 34 (1972), S. 457-466 
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    Notes: Abstract The solution of the diffusion equation in the gas phase of the human lung is very difficult because of the structure of the bronchial tree. It is shown by means of physical arguments, how one can reduce the diffusion equation to a simple one-dimensional form. The solution is then obtained by a stochastic simulation, which is easily realized on a digital computer.
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  • 18
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    Bulletin of mathematical biology 34 (1972), S. 467-481 
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    Notes: Abstract A new mathematical model of the oscillatory behavior of the respiratory center has been developed based upon published records of neuronal activity during respiration in the pons and medulla. In contrast with a previous model, four, rather than two, networks are assumed to interact in the respiratory center so as to produce the respiratory oscillation. A mathematical description of this interaction, in the form of a set of four first-order, nonlinear, coupled differential equations, is derived; the behavior of the solutions of this system is studied qualitatively, and expressions for the durations of the inspiratory and expiratory phases are obtained in terms of some parameters. It is found that central and chemical influences drive the medullar neurons to a position somewhere between saturation and full cutoff, and the pontine neurons deeply into cutoff. The control of the duration of the different phases by these chemical and central means is discussed. In order to effect a decrease in the magnitude of the various times, the neurons have to be driven towards operating points of higher central facilitation.
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  • 19
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    Bulletin of mathematical biology 34 (1972), S. 483-502 
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    Notes: Abstract In vivo control of calcium is analysed under the assumption that hormonal influences via plasma levels of parathormone and calcitonin are of prime (but not absolutely dominating) importance. A brief review concerning the physiological significance of body calcium and the mode of action of these two hormones is presented as an introduction to the basic philosophy of the study. A theoretical quasi-linear lumped-parameter model is developed to describe variations in ionic calcium, parathormone and calcitonin plasma concentrations to specific input stimuli. Formal evaluation of the system response requires the determination of ten constants, together with quantitation of ingested calcium entry into the plasma compartment which isindependent of hormonal influences. Values for various parameters are deduced from published data and experimental procedures are outlined to facilitate determination of the remaining unknowns. It is suggested that the proposed model should prove useful for investigations concerning general hormonal actions on calcium homeostatic mechanisms in both normal and diseased states, with particular reference to calcitonin.
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  • 20
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    Bulletin of mathematical biology 34 (1972), S. 521-532 
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    Notes: Abstract Ann species predator-prey chain is analyzed to determine what oscillations occur in population sizes. It is found that only the populations of the first and second species in the chain must necessarily oscillate around the point of equilibrium if they do not come to equilibrium. The other species may or may not oscillate.
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  • 21
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    Notes: Abstract Sangren and Sheppard developed a mathematical model for first-order processes taking place in the regional circulation, applicable—for example—to tracer studies of potassium transport. It permits calculation of specific activity at any point along a “tube of flow” or in the cuff of tissue surrounding it as a function of time following a spike injection of tracer. In efforts to relate to the exchange a rate curves obtained within vivo counters pointed at the region of interest, we developed a compartment-system model of the process. In investigating the properties of the Sangren and Sheppard model integrated over an entire circulatory bed, as thein vivo counter would see it, we found that when the distribution of transit times of the “tubes of flow” can be approximated by an exponential sum, the solution reduces to that of the compartment system model. This results in an important simplification in the calculation, and insight into the assumptions underlying the two different models. A curve-fitting computer program for the compartment model has been written and applied to double-isotope studies of potassium transport in the hind leg of the dog.
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  • 22
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    Bulletin of mathematical biology 34 (1972), S. 547-558 
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    Notes: Abstract Two chemicals,A andB, are allowed to diffuse together and a reaction described by $$A + B\mathop \rightleftharpoons \limits_{K_{ - 1} }^{K_1 } C$$ is allowed to proceed. This system is described mathematically by a system of partial differential equations. A numerical procedure is presented to find the rate constants ofK 1 andK −1. A systematic analysis of the effects of errors is also presented.
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  • 23
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    Bulletin of mathematical biology 34 (1972), S. 533-546 
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    Notes: Abstract Equations are developed to describe the energy expenditure of the human heart. As well as the external potential and kinetic energy terms, general consideration is given to other possible avenues of energy consumption. Emphasis is placed upon using mathematical variables which are readily available for experimental verification. The errors involved in assuming that mean values for the physiological parameters give reasonable estimations for the external mechanical performance are examined, and a theoretical estimation for the discrepancy in the kinetic component is presented. Logical extension of the mathematical derivation leads to a determination of cardiac external mechanical efficiency and clearly demonstrates the significance of the ventricular pressure-volume loop in this context. Finally, experimental procedures are suggested to clarify further some of the conclusions reached through the theoretical analysis.
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    Bulletin of mathematical biology 34 (1972), S. 559-563 
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    Notes: Abstract The question is discussed as to the reason why some animal societies, such as bees or ants, are sexually differentiated, that is, onlysome of its members are exhibiting reproducing activities. It is indicated that human society may be on its way to such a sexual differentiation which may eventually come.
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  • 25
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    Bulletin of mathematical biology 34 (1972), S. 565-565 
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  • 26
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    Bulletin of mathematical biology 34 (1972), S. 567-567 
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    Bulletin of mathematical biology 35 (1973), S. 301-311 
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    Notes: Abstract X-ray diffraction patterns obtained experimentally for fibers, together with their chemical structures, can be analyzed theoretically in terms of an integral equation. The partially unknown electron density function can be solved by iteration. This mathematical technique has been applied with success to study the secondary structures of DNA fibers.
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    Bulletin of mathematical biology 36 (1974), S. 339-340 
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  • 29
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    Bulletin of mathematical biology 36 (1974), S. 341-345 
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    Notes: Abstract For an environmental system described by a system of nonlinear first-order differential equations, the problem of achieving specified terminal conditions in a given time with a minimum expenditure of resources is considered. The initial conditions and the minimum value are found numerically in a particular example.
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    Bulletin of mathematical biology 36 (1974), S. 535-544 
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    Notes: Abstract A kinetic model of neural systems is introduced and discussed with statistical mechanics techniques. It is assumed that, for a macroscopic description of the model, it suffices to consider only the distribution for the velocity and position of the impulses, and the distribution for the excitation and position of the neurons, at any timet. Making use of Boltzmann's method for the study of a dilute gas, coupled differential equations for the rate of change with time of the distributions have been constructed.
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    Bulletin of mathematical biology 36 (1974), S. 457-476 
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    Notes: Abstract Creeping flow of a Newtonian fluid through a rigid permeable tube is considered and the transmural seepage is assumed to obey Darcy's law. Closed-form solutions for the pressure and velocity fields are presented and equations describing the axial variation of the mean cross-sectional pressure, the axial volumetric flow and the transmural fluid flux are derived. Approximate solutions for small seepage rates are given and are applied to the flow in the proximal renal tubule. Probable values for the epithelium permeability and the intraluminal hydrostatic pressure drop are obtained.
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    Bulletin of mathematical biology 35 (1973), S. 663-688 
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    Notes: Abstract The paper demonstrates that it is possible to construct memory models where the information inserted is stored in disseminated form, using sequential coding, the changes in the units forming the models being determined by their geometrical connections and by the incoming stream of information. The models are shown to have large storage capacity and their efficiency can be made insensitive to loss of or damage to a large fraction of their units. The satisfactory verification by computer simulation of the analysis and results described in the present paper will be the subject of a future paper.
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    Bulletin of mathematical biology 36 (1974), S. 605-605 
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    Bulletin of mathematical biology 36 (1974), S. 67-76 
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    Notes: Abstract We examine in detail Edward Kerner’s method for linearizing the equations of enzyme kinetics. Our main result is the determination of canonical forms for systems which can be linearized by the method. This is done both in general and in the special cases of two and three dimensions where complete results are obtained. The practical problem of identifying linearizable systems is also considered and computable necessary criteria are presented.
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    Notes: Abstract A general method for determination of the volume of a space in a non steady state condition, in case diffusion might be significant, is developed. Instantaneous mixing of indicators with native fluid is assumed in this first stage of investigation. Theoretical expressions are obtained for the volume of the space and the diffusion coefficient as a function of time. An analysis of feasibility of the method is also included.
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  • 36
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    Notes: Abstract The theory of transfer of low-molecular nonelectrolytes across deformable semipermeable membranes of large curvature developed in Part I (Rubinstein, 1974) is used to describe the dynamics of swelling and shrinking of a muscle fiber at the influx and efflux of low-molecular nonelectrolytes. A large set of computations showed that the theory explains the experiments described in the literature.
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    Bulletin of mathematical biology 36 (1974), S. 403-415 
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    Notes: Abstract Green's function for heat and matter transport is calculated for an infinite medium in which a convection field v(r,t) makes a contribution to the total heat and matter current. It is given by a uniformly and absolutely convergent series in which every term is calculated from the preceding one merely by integration. The solution procedure is interpreted physically and illustrated by a simple problem in which v(r,t)=const. in space and time. Since the solution contains no intrinsic spatial symmetry, it can serve as a starting point for a theory of heat and mass transport in perfused biological tissue.
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    Bulletin of mathematical biology 36 (1974), S. 435-444 
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    Notes: Abstract The hydrodynamics of a microorganism swimming in a channel is investigated. The microorganism is modeled as a two-dimensional sheet swimming at low Reynolds numbers between two rigid walls. The wavelengths of the propulsive waves passing down the sheet are assummed to be very large compared to the channel spacing, but the amplitude of the propulsive waves is arbitrary. Explicit analytical solutions for the propulsive velocity and the rate of energy dissipated in terms of the wave amplitude, channel spacing, wave number, and wave speeds are given.
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    Bulletin of mathematical biology 36 (1974), S. 455-456 
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    Bulletin of mathematical biology 36 (1974), S. 477-488 
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    Notes: Abstract It is shown from the statistical-mechanical overview of Volterra's ecological model how to reckon the fluctuations of collective variables such as the total population of a genus: and that these fluctuations are much decreased (or that the collective populationsteadiness is enhanced) as the speciation is increased. (A niching of species in time, or phase-niching, is entailed here.) Secondly, it is shown how Preston's log-normal distribution describing the species-abundance relationship, as well as a generalization of such distributions, come forth simply and naturally from the statistical-Volterra-dynamics.
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    Bulletin of mathematical biology 62 (2000), S. 37-59 
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    Notes: Abstract In Xenopus and Drosophila, the nucleocytoplasmic ratio controls many aspects of cell-cycle remodeling during the transitory period that leads from fast and synchronous cell divisions of early development to the slow, carefully regulated growth and divisions of somatic cells. After the fifth cleavage in sea urchin embryos, there are four populations of differently sized blastomeres, whose interdivision times are inversely related to size. The inverse relation suggests nucleocytoplasmic control of cell division during sea urchin development as well. To investigate this possibility, we developed a mathematical model based on molecular interactions underlying early embryonic cell-cycle control. Introducing the nucleocytoplasmic ratio explicitly into the molecular mechanism, we are able to reproduce many physiological features of sea urchin development.
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    Bulletin of mathematical biology 62 (2000), S. 17-35 
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    Notes: Abstract The irregular sequence of counts of a microbial population, in the absence of observable corresponding environmental changes (e.g., temperature), can be regarded as reflecting the interplay of several unknown or random factors that favor or inhibit growth. Since these factors tend to balance one another, the fluctuations usually remain within bounds, and only by a coincidence—when all or most act in unison—does an ‘outburst’ occur. This situation can be represented mathematically as a sequence of independent random variables governed by a probability distribution. The concept was applied to reported microbial counts of ground meat and wastewater. It is found that the lognormal distribution could serve as a model, and that simulations from this model are indistinguishable from actual records. The parameters of the lognormal (or other) distribution can then be used to estimate the probability of a population outburst, i.e., an increase above a given threshold. Direct estimation of the outburst probability based on frequency of occurrence is also possible, but in some situations requires an impractically large number of observations. We compare the efficiency of these two methods of estimation. Such methods enable translation of irregular records of microbial counts into actual probabilities of an outburst of a given magnitude. Thus, if the environment remains ’stable’ or in dynamic equilibrium, the fluctuations should not be regarded merely as noise, but as a source of information and an indicator of potential population outbursts even where obvious signs do not exist.
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    Bulletin of mathematical biology 62 (2000), S. 121-153 
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    Notes: Abstract During an immune response, the affinity of antibodies that react with the antigen that triggered the response increases with time, a phenomenon known as affinity maturation. The molecular basis of affinity maturation has been partially elucidated. It involves the somatic mutation of immunoglobulin V-region genes within antigen-stimulated germinal center B cells and the subsequent selection of high affinity variants. This mutation and selection process is extremely efficient and produces large numbers of high affinity variants. Studies of the architecture of germinal centers suggested that B cells divide in the dark zone of the germinal center, then migrate to the light zone, where they undergo selection based on their interaction with antigen-loaded follicular dendritic cells, after which they exit the germinal center through the mantle zone. Kepler and Perelson questioned this architecturally driven view of the germinal center reaction. They, as well as others, argued that the large number of point mutations observed in germinal center B cell V-region genes, frequently 5 to 10 and sometimes higher, would most likely render cells incapable of binding the antigen, if no selection step was interposed between rounds of mutations. To clarify this issue, we address the question of whether a mechanism in which mutants are generated and then selected in one pass, with no post-selection amplification, can account for the observed efficiency of affinity maturation. We analyse a set of one-pass models of the germinal center reaction, with decaying antigen, and mutation occurring at transcription or at replication. We show that under all the scenarios, the proportion of high affinity cells in the output of a germinal center varies logarithmically with their selection probability. For biologically realistic parameters, the efficiency of this process is in clear disagreement with the experimental data. Furthermore, we discuss a set of, possibly counterintuitive, more general features of one-pass selection models that follow from our analysis. We believe that these results may also provide useful intuitions in other cases where a population is subjected to selection mediated by a selective force that decays over time.
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    Bulletin of mathematical biology 62 (2000), S. 61-86 
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    Notes: Abstract Simple predator-prey models often predict extreme instability in interactions where the prey are depressed well below their carrying capacity. Although the behaviour of some laboratory systems conforms to this pattern, field and mesocosm studies generally show prolonged co-existence of prey and predator. Prominent among the possible causes of this discrepancy are the effects of spatial heterogeneity. In this paper we show that both discrete and continuous representations of the spatial Rosenzweig-McArthur model with immobile prey can be stabilized by self-organized prey heterogeneity. This concordance of behaviour closely parallels that which we have previously established in the context of invasion waves. We use the continuous model variant to calculate the characteristic spatial scales of the self-organized structures. The discrete variant forms the basis of a simulation study demonstrating the variety of stable structures and elucidating their relation to the history of the system. We note that all stable prey distributions take the form of a network of occupied patches separated by prey-free regions, and liken the process which generates such assemblages to the formation of a landscape mozaic.
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    Bulletin of mathematical biology 62 (2000), S. 395-398 
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    Bulletin of mathematical biology 62 (2000), S. 229-240 
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    Notes: Abstract Multistage mathematical models of carcinogenesis (when applied to tumor incidence data) have historically assumed that the growth kinetics of cells in the malignant state are disregarded and the formation of a single malignant cell is equated with the emergence of a detectable tumor. The justification of this simplification is, from a mathematical point of view, to make the estimation of tumor incidence rates tractable. However, analytical forms are not mandatory in the estimation of tumor incidence rates. Portier et al. (1996b, Math. Biosci. 135, 129–146) have demonstrated the utility of the Kolmogorov backward equations in numerically calculating tumor incidence. By extending their results, the cumulative distribution function of the time to a small observable tumor may be numerically obtained.
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    Bulletin of mathematical biology 62 (2000), S. 321-336 
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    Notes: Abstract An analytic formalism developed earlier to describe the time evolution of the basic enzyme reaction is extended to fully competitive systems. Time-dependent closed form solutions are derived for the three nominal cases of competition: even, slow and fast inhibitors, allowing for the first time the complete characterization of the reactions. In agreement with previous work, the time-independent Michaelis-Menten approach is shown to be inaccurate when a fast inhibitor is present. The validity of the quasi-steady-state approximation on which the present framework is based is also revised.
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    Bulletin of mathematical biology 62 (2000), S. 87-99 
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    Notes: Abstract A simple model of macroparasitic infections has been used to evaluate the potential use of parasites as biological tags of fish populations. In the model, the parasite-host interaction is regulated by a birth-death process, and parasites can only be acquired by the non-specific migratory host population in a particular area of the space domain. In this case, we show that parasites can be succesfully used for stocks identification and to describe the migratory routes taken by some marine fish species.
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    Bulletin of mathematical biology 62 (2000), S. 155-161 
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    Notes: Abstract We investigate the effect of migration between local populations of a single discrete-generation species living in a ring or an array of habitats. The commonly used symmetric dispersal assumption is relaxed to include the biologically more reasonable asymmetric dispersion. It is demonstrated analytically that density independent migration has no effect on the equilibrium stability of individual populations. However, the positive equilibrium may be destabilizing if the migration is density dependent in such a way that it increases with increasing population density at the source patch.
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    Bulletin of mathematical biology 62 (2000), S. 101-120 
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    Notes: Abstract A continuum model for a heterogeneous collection of excitable cells electrically coupled through gap junctions is introduced and analysed using spatial averaging, asymptotic and numerical techniques. Heterogeneity is modelled by imposing a spatial dependence on parameters which define the single cell model and a diffusion term is used to model the gap junction coupling. For different parameter values, single cell models can exhibit bursting, beating and a myriad of other complex oscillations. A procedure for finding asymptotic estimates of the thresholds between these (synchronous) behaviors in the cellular aggregates is described for the heterogeneous case where the coupling strength is strong. This procedure is tested on a model of a strongly coupled heterogeneous collection of bursting and beating cells. Since isolated pancreatic β-cells have been observed to both burst and beat, this test of the spatial averaging techniques provides a possible explanation to measured discrepancies between the electrical activities of isolated β-cells and coupled collections (islets) of β-cells.
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    Bulletin of mathematical biology 62 (2000), S. 595-632 
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    Notes: Abstract We describe the dynamics of competing species in terms of interactions between spatial moments. We close the moment hierarchy by employing a Gaussian approximation which assumes that fluctuations are independent and distributed normally about the mean values. The Gaussian approximation provides the lowest-order systematic correction to the mean-field approximation by incorporating the effect of fluctuations. When there are no fluctuations in the system, the mean equations agree with the Gaussian approximation as the fluctuations are weak. As the fluctuations gain strength, they influence the mean quantities and hence the Gaussian approximation departs from the mean-field approximation. At large fluctuation levels, the Gaussian approximation breaks down, as may be explained by the bimodality and skewness of the fluctuation distribution of the partial differential equation.
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    Notes: Abstract The multipole approach to the inverse electrocardiological problem consists of estimating the multipole components of the cardiac electric generator, starting from the measured body surface potential. This paper presents a critical investigation of the basic premise for the applicability of the multipole approach, namely the convergence of the multipole equivalent generator for the heart on the surface of an inhomogeneous body conductor. As an extension to multipole theory, a criterion for the convergence is derived. Based on realistic models for the body conductor and the cardiac electric generator, we observe that the criterion is not strictly satisfied in realistic conditions. Numerical simulations with the same models point out that the multipole equivalent generator is indeed not convergent in the strict mathematical sense. On the other hand, we show that the multipole equivalent generator yields a rather close approximation of the electrocardiological potential for intermediate values of the order of the multipole generator. A discussion is given on how to explain the apparently ambiguous results for the estimation of cardiac multipole components.
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    Bulletin of mathematical biology 62 (2000), S. 633-656 
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    Notes: Abstract The continuous model of Anderson et al. (1981), Nature 289, 765–771, is successful in describing certain characteristics of rabies epizootics, in particular, the secondary recurrences which follow the initial outbreak; however, it also predicts the occurrence of exponentially small minima in the infected population, which would realistically imply extinction of the virus. Here we show that inclusion of a more realistic distribution of incubation times in the model can explain why extinction will not occur, and we give explicit parametric estimates for the minimum infected fox density which will occur in the model, in terms of the incubation time distribution.
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    Bulletin of mathematical biology 62 (2000), S. 657-674 
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    Notes: Abstract The processes whereby developing neurones acquire morphological features that are common to entire populations (thereby allowing the definition of neuronal types) are still poorly understood. A mathematical model of neuronal arborizations may be useful to extract basic parameters or organization rules, hence helping to achieve a better understanding of the underlying growth processes. We present a parsimonious statistical model, intended to describe the topological organization of neuritic arborizations with a minimal number of parameters. It is based on a probability of splitting which depends only on the centrifugal order of segments. We compare the predictions made by the model of several topological properties of neurones with the corresponding actual values measured on a sample of honeybee (olfactory) antennal lobe neurones grown in primary culture, described in a previous study. The comparison is performed for three populations of segments corresponding to three neuronal morphological types previously identified and described in this sample. We show that simple assumptions together with the knowledge of a very small number of parameters allow the topological reconstruction of representative (bi-dimensional) biological neurones. We discuss the biological significance (in terms of possible factors involved in the determinism of neuronal types) of both common properties and cell-type specific features, observed on the neurones and predicted by the model.
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    Bulletin of mathematical biology 62 (2000), S. 483-499 
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    Notes: Abstract We re-visit previous analyses of the classical Michaelis-Menten substrate-enzyme reaction and, with the aid of the reverse quasi-steady-state assumption, we challenge the approximation d[C]/dt ≈ 0 for the basic enzyme reaction at high enzyme concentration. For the first time, an approximate solution for the concentrations of the reactants uniformly valid in time is reported. Numerical simulations are presented to verify this solution. We show that an analytical approximation can be found for the reactants for each initial condition using the appropriate quasi-steady-state assumption. An advantage of the present formalism is that it provides a new procedure for fitting experimental data to determine reaction constants. Finally, a new necessary criterion is found that ensures the validity of the reverse quasi-steady-state assumption. This is verified numerically.
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    Bulletin of mathematical biology 62 (2000), S. 799-848 
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    Notes: Abstract We analytically study the dynamics of evolving populations that exhibit metastability on the level of phenotype or fitness. In constant selective environments, such metastable behavior is caused by two qualitatively different mechanisms. On the one hand, populations may become pinned at a local fitness optimum, being separated from higher-fitness genotypes by a fitness barrier of low-fitness genotypes. On the other hand, the population may only be metastable on the level of phenotype or fitness while, at the same time, diffusing over neutral networks of selectively neutral genotypes. Metastability occurs in this case because the population is separated from higher-fitness genotypes by an entropy barrier: the population must explore large portions of these neutral networks before it discovers a rare connection to fitter phenotypes. We derive analytical expressions for the barrier crossing times in both the fitness barrier and entropy barrier regime. In contrast with ‘landscape’ evolutionary models, we show that the waiting times to reach higher fitness depend strongly on the width of a fitness barrier and much less on its height. The analysis further shows that crossing entropy barriers is faster by orders of magnitude than fitness barrier crossing. Thus, when populations are trapped in a metastable phenotypic state, they are most likely to escape by crossing an entropy barrier, along a neutral path in genotype space. If no such escape route along a neutral path exists, a population is most likely to cross a fitness barrier where the barrier is narrowest, rather than where the barrier is shallowest.
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    Bulletin of mathematical biology 62 (2000), S. 925-941 
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    Notes: Abstract Measures of sexual dimorphism have been used extensively to predict the social organization and ecology of animal and human populations. There is, however, no universally accepted measure of phenotypic differences between the sexes. Most indices of sexual dimorphism fail to incorporate all of the information contained in a random data set. In an attempt to have a better alternative, an index is proposed to measure sexual dimorphism in populations that are distributed according to a probabilistic mixture model with two normal components. The index calculates the overlap between two functions that represent the contribution of each sex in the mixture. In order to assess such an index, sample means, variances and sizes of each sex are needed. As a consequence, the sample information used is greater than that used by other indices that take intrasexual variability into account. By evaluating some examples, our proposed index appears to be a more realistic measure of sexual dimorphism than other measures currently used.
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    Bulletin of mathematical biology 62 (2000), S. 1001-1001 
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    Bulletin of mathematical biology 62 (2000), S. 1191-1194 
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    Bulletin of mathematical biology 62 (2000), S. 1087-1108 
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    Notes: Abstract While retinal defocus is believed to be myopigenic in nature, the underlying mechanism has remained elusive. We recently constructed a theory of refractive error development to investigate its fundamental properties. Our Incremental Retinal-Defocus Theory is based on the principle that the change in retinal-defocus magnitude during an increment of genetically-programmed ocular growth provides the requisite sign for the appropriate alteration in subsequent environmentally-induced ocular growth. This theory was tested under five experimental conditions: lenses, diffusers, occlusion, crystalline lens removal, and prolonged nearwork. Predictions of the theory were consistent with previous animal and human experimental findings. In addition, simulations using a MATLAB/SIMULINK model supported our theory by demonstrating quantitatively the appropriate directional changes in ocular growth rate. Thus, our Incremental Retinal-Defocus Theory provides a simple and logical unifying concept underlying the mechanism for the development of refractive error.
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    Bulletin of mathematical biology 62 (2000), S. 1163-1189 
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    Notes: Abstract A dynamic energy budget (DEB) model describes the rates at which organisms assimilate and utilize energy from food for maintenance, growth, reproduction and development. We study the dynamic behavior of one particular DEB model, Kooijman’s κ rule model, whose key assumption is that somatic and reproductive tissues are competing for energy. We assume an environment in which the food density fluctuates either periodically or stochastically (pink noise). Both types of fluctuations stimulate growth; the magnitude of the (average) increase in size depends on both the strength and duration of the fluctuations. In a stochastic environment, the risk of mortality due to starvation increases with increasing fluctuation intensity. The mean lifespan is also a function of the model parameter κ characterizing the partitioning of energy between somatic and reproductive tissues. Organisms committing a large fraction of resources to reproduction endure periods of food shortage relatively well. The effects of food fluctuations on reproduction are complex. With stochastic food, reproduction in survivors increases with increasing fluctuation intensities, but lifetime reproduction decreases. Periodic fluctuations may enhance reproduction, depending on the value of κ. Thus, a variable food supply stimulates growth, increases mortality and may enhance reproduction, depending on life history.
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    Transformation groups 5 (2000), S. 35-59 
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    Notes: Abstract In this paper we extend Drinfeld's current realization of quantum affine algebrasU q(ĝ) and of the Yangians in several directions: we construct current operators for non-simple roots of g, define a new braid group action in terms of the current operators, and describe the universalR-matrix for the corresponding “Drinfeld” comultiplication in the forms of an infinite product and of certain integrals over current operators.
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    Transformation groups 5 (2000), S. 325-350 
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    Notes: Abstract IfS=G Exp (iW) is a complex open Ol'shanskiî semigroup, whereW is an open elliptic cone, then we considerG-biinvariant domainsD=G Exp (iD g)S. First we show that the representation ofG×G on eachG-biinvariant irreducible reproducing kernel Hilbert space in Hol(D) is a highest weight representation whose kernel is the character of a highest weight representation ofG. In the second part of the paper we explain how to construct biinvariant Kähler structures on biinvariant Stein domains and show by a certain Legendre transform that the so obtained symplectic manifolds are isomorphic to domains in the cotangent bundleT * (G).
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    Transformation groups 5 (2000), S. 181-204 
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    Notes: Abstract We study Cartier divisors on normal varieties with the action of a reductive groupG. We give criteria for a divisor to be Cartier, globally generated and ample, and apply them to a study of the local structure and the intersection theory of aG-variety. In particular, we prove an integral formula for the degree of an ample divisor on a variety of complexity 1, and apply this formula to computing the degree of a closed 3-dimensional orbit in any SL2-module.
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    Bulletin of mathematical biology 11 (1949), S. 59-82 
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    Notes: Abstract A theory of linkage of autopolyploids is developed under consideration ofm loci andr alleles. The simplifying assumption of chromosome segregation, which may be considered as an approximation to the more adequate theory of chromatid segregation, is made throughout. Random mating and distinct, non-overlapping generations are assumed. Under these assumptions the problem is determined by three basic probability distributions—the distributions of genotypes and of gametes, and the segregation distribution. The segregation distribution is assumed to be the same for males and for females. The aim of the paper is to establish recurrence formulas (which allow to find the distributions of gametes and of genotypes from generation to generation, if the distribution of genotypes for an initial generation is known) and to investigate the limit behavior of these distributions as the number of generations increases indefinitely. In the present paper (hereafter referred to as I) the problem is explained, and the three characteristic distributions are introduced for the general case of a 2s-ploid,m loci, andr alleles. Recurrence relations are established for tetraploids,s=2 andm=2 loci, while the recurrence relations for the general case as well as the limit theorems will be given in the second part of this paper (hereafter referred to as II).
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    Bulletin of mathematical biology 11 (1949), S. 83-95 
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    Notes: Abstract Steady state kinetic relations previously developed forclosed, homogeneous systems are extended toopen systems consisting of geometrically confined regions of arbitrary shape. The generalized system of consecutive reactions is considered to occur within the cell, and the cell plus environment are treated as an open system. The diffusion condition is imposed upon the kinetic solution for various special cases and the method ofgeneral solution when all products, reactants and intermediates, may enter and leave the cell is indicated.
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    Bulletin of mathematical biology 11 (1949), S. 97-103 
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    Notes: Abstract When two polished metal spheres in contact with each other are immersed in a corrosive solution, their surfaces gradually corrode, leaving, however, a non-corroded zone around the point of contact. The size of this zone is a function of the size of the spheres, concentration of the corrosive, and of the time. The phenomenon has been first observed by F. C. Besic on human teeth immersed in hydrochloric acid, and studied on metal balls. In the present paper it is shown that such a phenomenon may be due to gradients of concentration of the corrosive in the neighborhood of the point of contact, caused by the chemical reaction which consumes the corrosive. Approximate expressions for the size of the uncorroded zones as a function of the size of the balls and as a function of time are derived and found to be in fair agreement with F. C. Besic's data.
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    Bulletin of mathematical biology 11 (1949), S. 105-113 
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    Notes: Abstract When an individual grows up in a society, he learns certain behavior patterns which are “accepted” by that society. He may in general have a tendency toward behavior patterns other than those which are “accepted” by the society. This tendency toward such unaccepted behavior may be due to a process of cerebration which results in doubt as to the “correctness” of the accepted behavior. Thus, on the one hand, the individual learns to follow the accepted rules almost automatically; on the other hand, he may tend to consciously break those rules. Using a neural circuit, suggested by H. D. Landahl in his theory of learning, a neurobiophysical interpretation of the above situation is outlined. Mathematical expressions are derived which describe the social behavior of an individual as a function of his age, social status, and some neurobiophysical parameters.
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    Bulletin of mathematical biology 11 (1949), S. 139-144 
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    Notes: Abstract Analysis is made to show that the mitotic index is simply proportional to the ratio of the duration of mitosis (T) to the intermitotic time only under special conditions. In the case of exponential growth of cell population the simple proportionality hold if the product ofT and the growth constant is small. For power law (t n ) growth of cell population the simple proportionality holds only when a steady state of growth has existed for at least ten intermitotic periods. The simple proportionality does not apply in conditions of transient growth.
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    Bulletin of mathematical biology 11 (1949), S. 115-138 
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    Notes: Abstract Food and metabolic waste products, insofar as they act upon the hereditary substrate of cells, are the most important factors governing tissue growth. Equations describing the growth of tissues are derived in consideration of this fact. A quantity is found in these equations which, if slightly changed, results in very great changes in the growth rate of the tissue, where such very great changes are interpretable as neoplastic growth. The relationship between our equations and similar equations which others have proposed is discussed.
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    Bulletin of mathematical biology 11 (1949), S. 145-147 
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    Bulletin of mathematical biology 33 (1971), S. 97-115 
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    Notes: Abstract A stochastic model is developed for an enzyme reaction in an open linear system. The proposed model assumes that the open system maintains the concentration of substrate and inhibitor at constant levels and that the product molecules are removed from the system by a first order reaction. Stochastic models for several enzyme reactions occurring in this open system are shown to correspond to special cases of theGI/M/∞ queue. Takács’ (1958) results for this queueing system are used to obtain the stochastic properties of the enzyme systems. A specific model we studied assumed completely competitive inhibition in an open system. The stationary distribution for the number of product molecules in the system is obtained. The enzyme reaction which incorporated the “intermediate chain hypothesis” can also be investigated by the queueing theory approach. It is shown that for this open system, if the model which incorporated the intermediate chain hypothesis has the same deterministic properties as the Michaelis-Menten model, then the latter has greater stochastic variation than the former.
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    Bulletin of mathematical biology 33 (1971), S. 153-153 
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    Bulletin of mathematical biology 33 (1971), S. 117-128 
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    Notes: Abstract The existing methods to solve the problems of pulsatile flow in the cardiovascular system are based on either linear axisymmetric equations or non-linear one-dimensional equations. The solutions thus obtained give only a mediocre comparison with measurements. In this paper, a non-linear axisymmetric theory is proposed. The starting point of the present theory is a third degree polynomial representation of the velocity profile. Integral methods are then applied to obtain the governing equations. To ascertain the accuracy of the theory proposed above, the calculations for a simple case involving pulsatile flow in a long rigid tube were performed. The results are: (a) the average velocities compare very well with exact solutions and (b) the velocity profiles for a given frequency agree very well with exact solutions for flow in small tubes, but tend to differ as tube size is increased.
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    Bulletin of mathematical biology 33 (1971), S. 129-151 
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    Notes: Résumé Le but de ce travail est la mise en évidence d’éventuels “patterns” temporels privilégiés de potentiels d’action neuronaux masqués par la superposition d’une activité aléatoire. Dans la première partie, on propose un modèle susceptible de rendre compte de cette activité aléatoire. Dans la seconde, on expose une méthode d’extraction des patterns privilégiés, compatible avec les paramètres du modèle neuronal proposé. Son algorithme fait notamment intervenir l’estimation de la fonction d’expectation. Cette méthode peut, en fait, ment intervenir l’estimation de la fonction d’expectation. Cette méthode peut, en fait, être appliquée à l’étude de séries temporelles d’événements dans des domaines très divers.
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    Bulletin of mathematical biology 33 (1971), S. 155-156 
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    Bulletin of mathematical biology 33 (1971), S. 355-372 
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    Notes: Abstract An effort is made to begin widening the scope of kinetics by merging the concepts and point of view of molecular set theory with the stochastic approach to kinetics, beginning with the simplest unimolecular molecular set transformation. In this spirit the new concept ofmolecular set variable is introduced as the basic unit of kinetics as opposed to simply the traditionalconcentration (or cardinality) unit, connoting that the composition as well as the size of a molecular set are significant dynamic features of a system. The changes in state (or “value”) of the molecular set variable are characterized by a Markovian stochastic process and the relationship between this process and the corresponding unimolecular process for the concentration variable introduced earlier is discussed. The possible role of molecular set theory in terms of the underlying biomathematical structure of relational biology is also considered.
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    Bulletin of mathematical biology 33 (1971), S. 387-401 
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    Notes: Abstract The problem of the forms of plants and models of branching are discussed using experimental data on the mistletoe. The number of branches by division, the distribution of divisions with regard to the number of branches per division and to the level of division, the geometrical characters of branches according to the level of division and the host, the stability of model are studied. One gives an interpretation of the model of branching as a model of growth.
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    Bulletin of mathematical biology 33 (1971), S. 373-386 
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    Notes: Abstract A quantum model for the general enzymic reaction,E+S ⇌ ES → P, is presented, starting with the assumptions that any chemical substanceS, which may be a substrate for a particularE (S)-enzyme is a microphysical system and any enzymeE-molecule, capable of interacting with anS-substrate is a “measuring system” which will “measure” one or more of theS-observables. According to the above assumptions a stochastic model of the reaction is constructed and a computer simulation of the steady state performed. The results thus obtained predicted fluctuations in the enzymic reaction rate, function of the substrate “perturbation”. On an experimental basis it is demonstrated that the irradiation of an enzymic substrate with low energies results in the inducement of a dose-dependent oscillatory behavior in the corresponding enzymic reaction rate. In the reaction type, the oscillations thus induced in theE-activity by the corresponding substrates are out-of-phase, realizing a biochemical discriminating net. Likewise, in an $$S_1 \xleftarrow{{E_1 }}S\xrightarrow{{E_2 }}S_2$$ reaction type, the oscillations induced by the irradiatedS-substrate in the activities of the respective enzyme, realize a biochemical switching net.
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    Bulletin of mathematical biology 34 (1972), S. 173-204 
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    Notes: Abstract As a further attempt to determine the stresses and strains of the individual myocardial fibers, the heart muscle is considered as an orthotropic material. A theory is presented which leads to the expression of the equilibrium conditions for the left ventricle in the form of three simultaneous differential equations. Solution of these equations would give the changes in shape of the left ventricle throughout the cardiac cycle, and, in addition, the stresses and strains of the individual myocardial fibers. It is pointed out, however, that meaningful solutions of the equations cannot be obtained at the present time because of difficulties in experimental determination of certain parameters.
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    Bulletin of mathematical biology 34 (1972), S. 213-222 
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    Notes: Abstract This paper compares two previously published neural models for epilepsies (Bull. Math. Biophysics,33, 539–553, 1971;34, 71–78, 1972). The second model is developed in more detail and an attempt is made to bring it more in line with established neurological findings. The question of classification of some epilepsies is briefly discussed.
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    Bulletin of mathematical biology 34 (1972), S. 223-230 
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    Notes: Abstract A formal mathematical model is proposed for a spontaneously repetitively firing neuron. It is based on the assumption that an excitatory and inhibitory substance, possibly different from those involved in synaptic transmissions, is formed in the soma of everynormal neuron. Furthermore, the decay of the substances is ascribed to their combination with some other substances, present in healthy individuals. A generalized two factor system of differential equations is used. It is shown that when the normally present substances are absent, possibly due to genetic defects so that the decay constants become zero, the equations lead to undamped sinusoidal solutions of the difference between excitatory and inhibitory factors, thus producing a trulyspontaneous repetitive discharge, in the absence of external currents or other stimulation. It is suggested that convulsants may act by destroying the substances present in healthy individuals. It is further suggested that by administering to epileptics those substances, which are present in normal healthy persons, perhaps by using brain extracts fromhealthy higher animals which sometimes suffer from epilepsy, an actual cure rather than symptomatic treatment by anticonvulsants may be obtained.
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    Bulletin of mathematical biology 34 (1972), S. 277-291 
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    Notes: Abstract The general kinetic behavior of a multicompartment system is shown to depend upon certain general structural features, including its connectivity, whether it is open, and whether it contains cyclic pathways. Structural influences are clarified by putting the system matrix in a certain form. For systems not strongly connected, a distinction is drawn between partially and completely open systems. Necessary and sufficient conditions are given for non-singularity of the system matrix and for asymptotic stability of the system. Sufficient conditions are given for non-overshooting and monotonic transitions. A system is demonstrated whose solution may contain a prolonged series of damped oscillations; but the oscillations are very slow and small; and it seems unlikely that oscillations could be detected experimentally in any biological system.
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    Bulletin of mathematical biology 34 (1972), S. 243-275 
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    Notes: Abstract It is shown how the fundamental laws of chemical kinetics for either open or closed systems with an arbitrarily large number of reactants can be represented as a system of Riccati-like differential equations. Through the use of a concise tensor notation, it is shown when and how the differential system is exactly reducible to linear form, a reduction without approximation that parallels the well-known similar reduction of a single simle Riccati equation. An example is worked out to show how open kinetics can lead to oscillatory chemical concentrations of the Change-Higgins type. The biologically central problem of great chemical speciation is discussed from the viewpoint of Gibbs ensemble theory within the linearized kinetics and, approximately, within the starting nonlinear kinetics where it is shown roughly how to estimate, from an overall temperature-like parameter characterizing the whole system, mean chemical levels and mean frequencies of oscillation, and where a gross oscillation of the total mass is estimated in terms of an anharmonic oscillator whose general structure is fixed from the structure of the chemical kinetic laws.
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    Bulletin of mathematical biology 34 (1972), S. 293-296 
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    Notes: Abstract A closed chain of compartments in which there is unidirectional transport between adjacent members can exhibit damped oscillations. For a system ofn equivalent compartments, the value ofn which gives the greatest difference between the first maximum and first minimum isn=11, the difference being 1.57%. The greatest difference between the first maximum value and the steady state value is 4% and is obtained whenn=25. The results are illustrated graphically forn equal to 5, 10, 25 and 100.
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    Bulletin of mathematical biology 34 (1972), S. 297-304 
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    Notes: Abstract This paper is a concrete approach to the problem of the number of the sexes. We try to imagine—on the example of three sexes—the mechanisms which would have to accompany a reproduction with several sexes. We have limited our study to the monohybridism, dihybridism and determinism of the sex.
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    Bulletin of mathematical biology 34 (1972), S. 325-335 
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    Notes: Abstract An analysis of the effect of cilia on fluid transport in tubules is presented. The applicability of the results for the flow rates observed in the ductus efferentes of the male tract is discussed.
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    Bulletin of mathematical biology 34 (1972), S. 305-324 
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    Notes: Abstract The dipole models for steady-state currents in excitable membranes of Arndt, Bond and Roper and of Hamel and Zimmerman are compared by fitting the equations to the data of Gilbert and Ehrenstein. The more complex Hammel and Zimmerman model does not fit the data as well as does the simpler Arndt, Bond and Reper model. When fitting the data, the Hammel and Zimmerman current equation reduces to the Arndt, Bond and Roper current equation because of the values assumed by the parameters. An interpretation is given for the parameter values obtained with the Arndt, Bond and Roper model.
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    Bulletin of mathematical biology 34 (1972), S. 337-341 
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    Notes: Abstract It is shown that, under rather general conditions, it is possible to formally decompose the dynamics of ann-dimensional dynamical system into a number of non-interacting subsystems. It is shown that these decompositions are in general not simply related to the kinds of observational procedures in terms of which the original state variables of the system are defined. Some consequences of this construction for reductionism in biology are discussed.
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    Bulletin of mathematical biology 34 (1972), S. 343-353 
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    Notes: Abstract For a certain class of physical machines, termed “structure-determined,” the problem of self-reproduction can be reduced to the problem of serial message reproduction. Serial message reproduction however presupposes a sort of “open system” constraint. This leads to the principle of pseudo, or exogenously standardized, respectively, self-reproduction. It seems to be consistent with both chemical and biological self-reproduction. It thus may reflect a general principle of biological design. The proposed principle is a physico chemical analog to Robert Rosen's abstract relational self-reproduction constraint.
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    Bulletin of mathematical biology 34 (1972), S. 355-377 
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    Notes: Abstract Equations are derived describing potentials due to an active muscle fiber in an infinite medium in terms of two surface integrals—one of the propagated action potential and the other of the membrane current density, both integrals being taken over the surface of the muscle. These equations are incorporated into an equivalent cardiac current generator in which the left ventricle (i.e. the current source) is represented by a three-dimensional wedge and the thorax (i.e. the volume conductor), by a homogeneous circular cylinder. Since this current generator expresses the body surface potentials in terms of the membrane current density and the membrane potential at any point on the surface of the electrically active muscle fiber, the calculated ECG can be correlated with theactual sources within the heart. This equivalent cardiac generator possesses many of the physical and physiological properties of cardiac muscle. The equations were evaluated numerically on a digital computer. The results indicate that equivalent cardiac current generators of this type can yield clinically significant results and that further research is necessary to investigate their properties fully.
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    Bulletin of mathematical biology 34 (1972), S. 413-418 
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    Notes: Abstract Analytical solutions are presented for transient heat conduction in biological media. General boundary conditions and internal sources varied in both spatial and time variables are considered, thus, solutions for many special cases can be obtained with ease from the general solutions presented in this analysis.
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    Bulletin of mathematical biology 34 (1972), S. 393-412 
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    Notes: Abstract Two mathematical models of pulmonary single breath gas washout (one analytic, one numerical) are developed and their predictions compared with experimental data on human subjects. Weibel's 23 generation symmetric anatomical model is used as a guide to bronchial tree geometry. Experimental plots of nitrogen concentration versus volume expired, dead space versus breath holding time, and dead space versus tidal volume are compared with plots predicted by the models. Agreement is good. A plot of nitrogen concentration in the airways as predicted by the numerical model at different times during inhalation and exhalation of a single breath of oxygen is shown. Model predictions for changes in dead space with changes in washout gas and expiratory flow rate are discussed. Use of the analytic model for obtaining average values of the path length from mouth to alveoli in a given subject is discussed. To the extent of their agreement with experiment, the models provide a sound physical basis for the correlation of airway structure and function.
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    Bulletin of mathematical biology 34 (1972), S. 429-429 
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    Bulletin of mathematical biology 34 (1972), S. 419-427 
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    Notes: Abstract The Roginsky-Zeldovich (or Elovich) equation, which is −dx/dt=m exp (nx) (x=substrate concentration,t=time,m andn=constants), describes the kinetics of various biological electron and ion transport processes, and has been derived from the concept of charge transport across an activation energy barrier at an interface between dissimilar phases, driven by a difference in redox or ion potentials, with the simplifying assumptions that charge carrier concentration is constant, backward current across the interface is zero, and diffusion of substrate is fast. If charge carrier concentration is proportional to substrate concentration, then the kinetic equation is −dx/dt=mx exp (nx). If backward current is not zero, then −dx/dt=m 1 exp (n 1x) −m 2 exp (n 2 x), wherem 1,m 2,n 1 andn 2 are constants. Kinetic equations for interfacial charge transport in the presence of a significant substrate diffusion potential are also derived.
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    Bulletin of mathematical biology 35 (1973), S. 313-317 
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    Notes: Abstract Various philosophers have repeatedly denounced knowledge as a source of unpleasantness, thereby criticizing education. This paper presents a set theoretical approach to knowledge and education and tries to explain how they could lead occasionally to a feeling of unpleasantness.
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    Bulletin of mathematical biology 35 (1973), S. 275-286 
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    Notes: Abstract An analysis of countercurrent exchange in a U-tube is presented for a single-solute, constant-volume flow rate system with spatially varying source fluxes and permeabilities. Analytical solutions are given for the steady-state equations and numerical solutions for the unsteady-state equations. The solutions indicate that an external source of solute delivered to the stream flowing away from the U-tube bend can be distributed by the exchanger so that the concentration in both limbs increases toward the bend. In particular, there exist source fluxes whose magnitude decreases monotonically toward the bend for which the maximum solute concentration occurs at the bend. The point at which a concentration maximum occurs is governed principally by the solute permeability of the barrier separating the two limbs and by the volume flow rate through the exchanger. The system dynamics depend strongly on the relative cross-sectional areas of the two limbs or, equivalently, on the flow velocities within them. The model is used as a basis for discussion of various functional aspects of the renal vasa recta system.
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    Bulletin of mathematical biology 35 (1973), S. 287-300 
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    Notes: Abstract The circulatory mixing process was analyzed as the time course of the dispersion of indicator after its injection into the heart. In simplified models, which had one or two lumped mixing chambers and circulatory pathways connected with them, it was suggested that the extent of dispersion could be evaluated by the variance of indicator distribution in the total circulating blood when the circulation time distributions between the chambers and the concentration curves in the chambers were known. The method of determining the circulation time distributions through the pulmonary, systemic and total circulations was derived and the actual distributions were obtained in dogs by indicator dilution techniques. With the use of these distributions, the time course of the circulatory mixing process was numerically calculated. The results showed that there was considerable difference in velocities of the process between the case of the right heart injection and the left heart injection of the indicator.
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    Bulletin of mathematical biology 35 (1973), S. 319-337 
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    Notes: Abstract An investigation is made as to whether or not the existence of a band-pass filter function, analogous to that in electronics, can be proved from the fundamental laws of chemical kinetics. The problem is important for better understanding of the preference of certain biological rhythms to others. It is shown with simple examples that such behavior is possible for a number of systems of coupled chemical reactions far enough from the thermodynamic equilibrium. It is of interest to generalize this behavior since it could conceivably play a role in the transmission of “usable information” in biology.
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    Bulletin of mathematical biology 35 (1973), S. 339-344 
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    Notes: Abstract The phenomenon of mental creativity is considered from the standpoint of the theory of organismic sets, developed by the author in a series of previous publications. It is shown how the differences in creativity between different individuals may be interpreted on this basis, and why extreme creativity is rare. A parallel interpretation for facility in observation is given, and it is shown why facility in creativity and observation is much rarer than either individual facility. A further conclusion is drawn regarding the deducibility of the laws of nature by purely logical means.
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