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  • 1
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    Bulletin of mathematical biology 56 (1994), S. 129-146 
    ISSN: 1522-9602
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Mathematics
    Notes: Abstract More than 20 years after its proposal, Keller and Segel's model (1971,J. theor. Biol.,30, 235–248) remains by far the most popular model for chemical control of cell movement. However, before the Keller-Segel equations can be applied to a particular system, appropriate functional forms must be specified for the dependence on chemical concentration of the cell transport coefficients and the chemical degradation rate. In the vast majority of applications, these functional forms have been chosen using simple intuitive criteria. We focus on the particular case of eukaryotic cell movement, and derive an approximation to the detailed model of Sherrattet al. (1993,J. theor. Biol.,162, 23–40). The approximation consists of the Keller-Segel equations, with specific forms predicted for the cell transport coefficients and chemical degradation rate. Moreover, the parameter values in these functional forms can be directly measured experimentally. In the case of the much studied neutrophil-peptide system, we test our approximation using both the Boyden chamber and under-agarose assays. Finally, we show that for other cell-chemical interactions, a simple comparison of time scales provides a rapid check on the validity of our Keller-Segel approximation.
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  • 2
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    Bulletin of mathematical biology 56 (1994), S. 1-64 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract The formal structure of evolutionary theory is based upon the dynamics of alleles, individuals and populations. As such, the theory must assume the prior existence of these entities. This existence problem was recognized nearly a century ago, when DeVries (1904,Species and Varieties: Their Origin by Mutation) stated. “Natural selection may explain the survival of the fittest, but it cannot explain the arrival of the fittest.” At the heart of the existence problem is determining how biological organizations arise in ontogeny and in phylogeny. We develop a minimal theory of biological organization based on two abstractions from chemistry. The theory is formulated using λ-calculus, which provides a natural framework capturing (i) the constructive feature of chemistry, that the collision of molecules generates specific new molecules, and (ii) chemistry's diversity of equivalence classes, that many different reactants can yield the same stable product. We employ a well-stirred and constrained stochastic flow reactor to explore the generic behavior of large numbers of applicatively interacting λ-expressions. This constructive dynamical system generates fixed systems of transformation characterized by syntactical and functional invariances. Organizations are recognized and defined by these syntactical and functional regularities. Objects retained within an organization realize and algebraic structure and possess a grammar which is invariant under the interaction between objects. An organization is self-maintaining, and is characterized by (i) boundaries established by the invariances, (ii) strong self-repair capabilities responsible for a robustness to perturbation, and (iii) a center, defined as the smallest kinetically persistent and self-maintaining generator set of the algebra. Imposition of different boundary conditions on the stochastic flow reactor generates different levels of organization, and a diversity of organizations within each level. Level 0 is defined by selfcopying objects or simple ensembles of copying objects. Level 1 denotes a new object class, whose objects are self-maintaining organizations made of Level 0 objects, and Level 2 is defined by self-maintaining metaorganizations composed of Level 1 organizations. These results invite analogy to the history of life, that is, to the progression from self-replication to self-maintaining procaryotic organizations to ultimately yield self-maintaining eucaryotic organizations. In our system self-maintaining organizations arise as a generic consequence of two features of chemistry, without appeal to natural selection. We hold these findings as calling for increased attention to the structural basis of biological order.
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  • 3
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    Bulletin of mathematical biology 56 (1994), S. 249-273 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract A model is developed to describe neuronal elongation as a result of the polymerization of microtubules and elastic stretching of the neurites by force produced by the growth cone. The model for a single segment with a single growth cone revealed a constant elongation rate, while the concentration of tubulin in the soma rises, and the concentration of tubulin becomes constant in the growth cone. Extending the model to a neurite with a single branch point and two growth cones revealed the same results. When the assembly or the disassembly rate of microtubules is unequal in both growth cones, transient retraction of one of the terminal segments occurs, which results in complete retraction of the segment when the difference in (dis)assembly rate between the two growth cones is large enough. When the model is applied to large trees, a maximal sustainable number of terminal segments as a function of the production rate of tubulin appears. Mechanisms to stop outgrowth are discussed in relation to the establishment of synaptical contacts between cells.
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  • 4
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    Bulletin of mathematical biology 56 (1994), S. 225-247 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract We have developed a new model describing the relationship between plasma and red cell tracers flowing through the lung. The model is the result of an analysis of the transport of radiolabeled plasma albumin between two flowing phases and shows that differences between red cell and plasma tracer curves are related to microvascular hematocrit. The model was tested in an isolated, blood-perfused dog lung preparation in which we injected51Cr-labeled red cells and125I-labeled plasma albumin into the pulmonary artery. From the tracer concentration-time curves at the venous outflow, we calculatedh r, the ratio of microvascular hematocrit to large-vessel hematocrit. In 18 baseline experiments,h r=0.92±0.01 (mn±sem) at a blood flow rate of 10.7±0.3 ml s−1. We determined the effects of (a) glass bead embolization, (b) alloxan, and (c) lobe ligation onh r. Embolization attenuated the separation between plasma and red cells (increasedh r), probably as a consequence of passive vasodilation. Alloxan enhanced separation of plasma and red cells (decreasedh r), possibly as a result of arteriolar vasoconstriction. Ligation of a fraction of the perfused tissue at constant flow did not cause significant change inh r in the remaining perfused tissue. The model assumes that large-vessel transit times are uniform and that all dispersion occurs in the microvasculature. A theoretical analysis apportioning dispersion between large and small vessels disclosed that the error associated with these assumptions is likely to be less than 15% of the measuredh r. We conclude from this study that the microvascular hematocrit model describes experimental plasma and red cell curves. The results imply thath r can be readily deduced from tagged red cells and plasma and can be accounted for in calculating permeability-surface area in diffusing tracer experiments.
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  • 5
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract We present a mathematical model of the cytotoxic T lymphocyte response to the growth of an immunogenic tumor. The model exhibits a number of phenomena that are seenin vivo, including immunostimulation of tumor growth, “sneaking through” of the tumor, and formation of a tumor “dormant state”. The model is used to describe the kinetics of growth and regression of the B-lymphoma BCL1 in the spleen of mice. By comparing the model with experimental data, numerical estimates of parameters describing processes that cannot be measuredin vivo are derived. Local and global bifurcations are calculated for realistic values of the parameters. For a large set of parameters we predict that the course of tumor growth and its clinical manifestation have a recurrent profile with a 3- to 4-month cycle, similar to patterns seen in certain leukemias.
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  • 6
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    Bulletin of mathematical biology 56 (1994), S. 275-294 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract We present a new, practical algorithm to resolve the experimental data in restriction site analysis, which is a common technique for mapping DNA. Specifically, we assert that multiple digestions with a single restriction enzyme can provide sufficient information to identify the positions of the restriction sites with high probability. The motivation for the new approach comes from combinatorial results on the number of mutually homeometric sets in one dimension, where two sets ofn points are homeometric if the multiset ofn(n−1)/2 distances they determine are the same. Since experimental data contain errors, we propose algorithms for reconstructing sets from noisy interpoint distances, including the possibility of missing fragments. We analyse the performance of these algorithms under a reasonable probability distribution, establishing a relative error limit ofr=Θ(1/n 2) beyond which our technique becomes infeasible. Through simulations, we establish that our technique is robust enough to reconstruct data with relative errors of up to 7.0% in the measured fragment lengths for typical problems, which appears sufficient for certain biological applications.
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    Bulletin of mathematical biology 56 (1994), S. 323-336 
    ISSN: 1522-9602
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    Notes: Abstract A simple chemical model of the idiotypic network of immune systems, namely the AB model, has been developed by De Boeret al. The complexity of the system, such as the steady states, periodic oscillations and chaotic motions, has been examined by the authors mentioned above. In the present paper, the periodic motions and chaotic behaviours exhibited by the system are intuitively described. To clarify in which parameter domains concerned the system exhibits periodic oscillations and in which parameter domains the system demonstrates chaotic behaviours the Lyapounov exponent is explored. To characterize the strangeness of the attractors, the fractal dimension problem is worked out.
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  • 8
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    Bulletin of mathematical biology 56 (1994), S. 359-363 
    ISSN: 1522-9602
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  • 9
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    Bulletin of mathematical biology 56 (1994), S. 337-357 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract We consider a stochastic mechanism of the loss of resistance of cancer cells to cytotoxic agents, in terms of unstable gene amplification. Two models being different versions of a time-continuous branching random walk are presented. Both models assume strong dependence in replication and segregation of the extrachromosomal elements. The mathematical part of the paper includes the expression for the expected number of cells with a given number of gene copies in terms of modified Bessel functions. This adds to the collection of rare explicit solutions to branching process models. Original asymptotic expansions are also demonstrated. Fitting the model to experimental data yields estimates of the probabilities of gene amplification and deamplification. The thesis of the paper is that purely stochastic mechanisms may explain the dynamics of reversible drug resistance of cancer cells. Various stochastic approaches and their limitations are discussed.
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  • 10
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    Bulletin of mathematical biology 56 (1994), S. 365-368 
    ISSN: 1522-9602
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  • 11
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    Bulletin of mathematical biology 56 (1994), S. 369-389 
    ISSN: 1522-9602
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    Topics: Biology , Mathematics
    Notes: Abstract Dextran has been the most commonly employed test molecule for probing the selectivity of glomerular filtration to macromolecules of varying size. The usual theories for hindered transport of solid spheres through pores have limited utility in interpreting clearance data for dextran or other linear polymers because such polymers in solution more closely resemble random, solvent-filled coils than solid spheres. To provide a model for glomerular filtration of random-coil macromolecules, the equilibrium partitioning of random coils between cylindrical pores and bulk solution was simulated using Monte Carlo calculations, and those results were combined with a hydrodynamic theory for restricted motion of solvent-filled polymer coils in pores. The rates of transport predicted for either neutral random coils or for solid spheres of the same Stokes-Einstein radius were significantly lower than observed transport rates of dextran through the glomerular capillary wall or across synthetic porous membranes. This facilitation of dextran transport was modeled by postulating weak, attractive interactions between dextran monomers and the pore wall. The random-coil model with attractive interactions, modeled using a short-range, square-well potential, was found to adequately represent dextran sieving data in normal rats. Various limitations of this approach are discussed.
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    Bulletin of mathematical biology 56 (1994), S. 567-586 
    ISSN: 1522-9602
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    Notes: Abstract Method-dependent mechanisms that may affect dynamic numerical solutions of a hyperbolic partial differential equation that models concentration profiles in renal tubules are described. Some numerical methods that have been applied to the equation are summarized, and ways by which the methods may misrepresent true solutions are analysed. Comparison of these methods demonstrates the need for thoughtful application of computational mathematics when simulating complicated time-dependent phenomena.
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  • 13
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    Bulletin of mathematical biology 56 (1994), S. 587-616 
    ISSN: 1522-9602
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    Notes: Abstract The regulation of the interactions between the actin binding proteins and the actin filaments are known to affect the cytoskeletal structure of F-actin. We develop a model depicting the formation of actin cytoskeleton, bundles and orthogonal networks, via activation or inactivation of different types of actin binding proteins. It is found that as the actin filament density increases in the cell, a spontaneous tendency to organize into bundles or networks occurs depending on the active actin binding protein concentration. Also, a minute change in the relative binding affinity of the actin binding proteins in the cell may lead to a major change in the actin cytoskeleton. Both the linear stability analysis and the numerical results indicate that the structures formed are highly sensitive to changes in the parameters, in particular to changes in the parameter ϕ, denoting the relative binding affinity and concentration of the actin binding proteins.
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  • 14
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    Bulletin of mathematical biology 56 (1994), S. 633-664 
    ISSN: 1522-9602
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    Notes: Abstract To investigate morphogenesis and in particular circularization mechanisms in young mycelia, we observe cultures of the zygomyceteMucor spinosus and develop discrete models of two-dimensional filamental branching growth. The models are based on the hypothesis that the fungus secretes a regulatory substance that diffuses into the surrounding medium and is detected by the growing hyphae. We also present a simple Markovian growth model without such a feedback, but yielding to analytical computations.
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    Bulletin of mathematical biology 56 (1994), S. 617-631 
    ISSN: 1522-9602
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    Notes: Abstract In vivo volume growth of two murine tumor cell lines was compared by mathematical modeling to their volume growth as multicellular spheroids. Fourteen deterministic mathematical models were studied. For one cell line, spheroid growth could be described by a model simpler than needed for description of growthin vivo. A model that explicitly included the stimulatory role for cell-cell interactions in regulation of growth was always superior to a model that did not include such a role. The von Bertalanffy model and the logistic model could not fit the data; this result contradicted some previous literature and was found to depend on the applied least squares fitting method. By the use of a particularly designed mathematical method, qualitative differences were discriminated from quantitative differences in growth dynamics of the same cells cultivated in two different three-dimensional systems.
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    Bulletin of mathematical biology 56 (1994), S. 665-686 
    ISSN: 1522-9602
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    Notes: Abstract This paper develops and applies a dynamic mathematical model for optimal scheduling of nitrogen fertilization and irrigation that minimizes nitrogen leaching subject to a target level of yield. The analysis assumes a single crop grown during a single growing season of a given length. It is shown that substitution of water for nitrogen along a given plant growth path decreases nitrogen leaching and, therefore, groundwater contamination. It is proved that a minimum leaching solution to the optimization problem is obtained with a single nitrogen application at the beginning of the season and irrigation scheduling that maintains a wet soil throughout the growing period. A numerical example utilizing experimental data for an irrigated summer corn in Israel confirms and quantifies the analytical findings.
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    Bulletin of mathematical biology 56 (1994), S. 875-898 
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    Notes: Abstract We analyse the stochastic properties of dynamical systems with finite populations of a few differentreplicator species. Our main interest is to evaluate the typicallifetime, i.e. the time for the extinction of the first species in the network, for different catalytic structures, as a function of the population size.
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    Bulletin of mathematical biology 56 (1994), S. 899-921 
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    Notes: Abstract The capacity of a model immune network in terms of the number of different antigens that can be vaccinated against without any memory lost is computed and tested by numerical simulations. We also investigate memory loss and failure to vaccinate due to overcrowding the network with too many antigens. The computations are done for two different strategies for proliferation, one implying all the antigen specific clones and the second one being more thrifty.
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    Bulletin of mathematical biology 56 (1994), S. 923-943 
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    Notes: Abstract The technique of model-building a protein of known sequence but unknown tertiary structure from the structures of homologous proteins is probably so far the most reliable means of mapping from primary to tertiary structure. A key step towards the realization of the aim is to develop ways of aligning three-dimensional structures of homologus proteins, thereby deriving the rules useful for protein modelling. We have developed a generalized differential-geometric representation of protein local conformation for use in a protein comparison program which aligns protein sequences on the basis of their sequence and conformational knowledge. Because the differetial-geometric distance measure between local conformations is independent of the coordinate frame and remains chirality information, the comparison program is easily implemented, relatively rational and reasonably fast. The utility of this program for aligning closely and distantly related homologous proteins is demonstrated by multiple alignment of globins, serine proteinases and aspartic proteinase domains. Particularly, the method has reached the rational alignment between the mammalian and microbial serine proteinases as compared with many published alignment programs.
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    Bulletin of mathematical biology 56 (1994), S. 945-957 
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    Notes: Abstract New formulas for deriving the sensitivities of stable stage structures and reproductive values to changes in vital rates are presented. They enable comparison of the sensities to changes of different elements in the projection matrix; in other words, comparison of partial derivatives of the eigenvectors. These kinds of sensitivities can be used in applied problems such as an analysis of the effect of harvesting on the population structure. However, in this paper, we examine the application of the sensitivities in a more general ecological context. We investigate why the stable stage structure of the mustard aphid,Lipaphis erysimi, changes very little in the temperature interval 10–30°C. The sensitivities of the stable stage structure at 15°C and 25°C were derived. The character of the sensitivites were the same in both temperatures although the stage structure was more sensitive to changes at 15°C than at 25°C. The sensitivity analysis also revealed that the temperature variation results in changes in fecundity and developmental rate that have a counteractive effect on the population structure.
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    Bulletin of mathematical biology 56 (1994), S. 981-998 
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    Notes: Abstract Plankton populations undergo dramatic surges. Rapid increases and decreases by a factor of 10 or more are observed, often separated by relatively stable interludes. We propose a description of plankton communities as excitable systems. In particular, we present a model for the evolution of phytoplankton and zooplankton populations which resembles models for the behaviour of excitable media. The parameter dependency of the various “excitable” phenomena, trigger mechanism, threshold, and slow recovery, is clear, and permits ready investigation of the influence of properties of the physical environment, including variations in nutrient fluxes, temperature or pollution levels.
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    Bulletin of mathematical biology 56 (1994), S. 959-980 
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    Notes: Abstract Analysis schemes for the classification of synergism and antagonism for mixed agents operate on the discrepancies between observed and calculated results. As such they cannot be confirmed by experiments and therefore have to be tested in terms of mathematical and logical self-consistency. The concept of independent action is close to the literal meaning of the term “non-interaction”. Since this concept does not depend on the mechanisms of actions nor on the type of effect scale used, it is suitable as one of the basic criterion for the definition of synergism and antagonism. A general mathematical framework of independent action is presented in this paper based on the concept of “relative effect” as used in the literature. The, different equations for independent action currently used in various areas are shown to be manifestations, of a general formula under different sets of boundary conditions, which are the natural limiting values of the effects of the corresponding system observed at low and at high doses of the agents. The framework can, be generalized to the combined action ofn-agents as well as to the interaction of an agent with itself. In addition, the differential form of the formula for independent action is derived. This framework of systematic definitions and derived equations enable a more in-depth study of the implications of the concept of independent action and its relation to other concepts of non-interaction.
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    Bulletin of mathematical biology 56 (1994), S. 999-1008 
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    Bulletin of mathematical biology 56 (1994), S. 1009-1040 
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    Notes: Abstract We model how auto-reactiveB cells are kept under control by an idiotypic network. Autoimmunity occurs when the control is broken by an infection or not achieved through an abnormal ontogenetic evolution. We describe the idiotypic network, viz., the central immune system, by idiotype-anti-idiotype pairs which are coupled to a set of highly connected clones, which interact with each clone of the network. Some clones of the central immune system recognize self-antigen. We find a huge variety of fixed points which can be classified as tolerant, autoimmune, and neutral states according to the concentration of the auto-reactive antibody. Most significant are auto-reactive clones which are a member of an idiotype-anti-idiotype pair. In a healthy individual, an autoimmune disease is induced by an antigen infection which triggers a transition from a tolerant to an autoimmune state. Autoimmunity is induced more readily by an antigen coupling to theanti-idiotype than by one interacting with the auto-reactive clone itself. We indicate a possible therapy which simply reverses the processes that have lead to the autoimmune disease. In the early development of the central immune system its highly connected, core part serves to draw the more specific clones of idiotype-anti-idiotype pairs into the network. In order to avoid autoimmunity in ontogenetic evolution the anti-idiotype of an auto-reactive clone must be formed in advance by a sufficiently long period of time. Thus, a well ordered succession of the appearance of the more specific clones is required.
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    Bulletin of mathematical biology 56 (1994), S. 1121-1141 
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    Notes: Abstract A method of dimensionless time-scaling based on extrinsic expectation of life at birth but intrinsic to a system generating a survival distribution is introduced. Such scaling allows the survival fraction function and its associated mortality function to serve as Green's functions for their generalized equivalents. i.e. a “population” function and a “death” function. The analytical mechanics of utilizing these concepts are formulated, applied to the classical Gompertz and Weibull survival models, and discussed with respect to biological relevance.
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    Bulletin of mathematical biology 56 (1994), S. 1095-1119 
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    Notes: Abstract It is now widely accepted that localized high concentrations of Ca2+ (Ca2+ domains) play a major role in controlling the time course of neurotransmitter release. In the present work we calculate the magnitude and the time course of Ca2+ domains that evolve in the vicinity of a Ca2+ channel and an adjacent release site. In the calculations we consider a accurately dimensioned Ca2+ channel. Moreover, the Ca2+ current is continuously adjusted with regard to the accumulated intracellular Ca2+ and, in addition, endogenous buffers are considered. The calculations, carried out by the software FIDAP, based on finite element method, show that the Ca2+ concentrations achieved near the release sites are significantly lower than claimed by other investigators. Furthermore, we present arguments indicating that the Ca2+ domains, regardless of their magnitude, do not play a role in controlling the time course of release of neurotransmitter.
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    Bulletin of mathematical biology 56 (1994), S. 1041-1093 
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    Notes: Abstract Mammalian white blood cells are known to bias the direction of their movement along concentration gradients of specific chemical stimuli, a phenomenon called chemotaxis. Chemotaxis of leukocyte cells is central to the acute inflammatory response in living organisms and other critical physiological functions. On a molecular level, these cells sense the stimuli termed chemotactic factor (CF) through specific cell surface receptors that bind CF molecules. This triggers a complex signal transduction process involving intracellular biochemical pathways and biophysical events, eventually leading to the observable chemotactic response. Several investigators have shown theoretically that statistical fluctuations in receptor binding lead to “noisy” intracellular signals, which may explain the observed imperfect chemotactic response to a CF gradient. The most recent dynamic model (Tranquillo and Lauffenburger,J. Math. Biol. 25, 229–262. 1987) couples a scheme for intracellular signal transduction and cell motility response with fluctuations in receptor binding. However, this model employs several assumptions regarding receptor dynamics that are now known to be oversimplifications. We extend the earlier model by accounting for several known and speculated chemotactic receptor dynamics, namely, transient G-protein signaling, cytoskeletal association, and receptor internalization and recycling, including statistical fluctuations in the numbers of receptors among the various states. Published studies are used to estimate associated constants and ensure the predicted receptor distribution is accurate. Model analysis indicates that directional persistence in uniform CF concentrations is enhanced by increasing rate constants for receptor cytoskeletal inactivation, ternary complex dissociation, and binary complex dissociation, and by decreasing rate constants for receptor internalization and recycling. For most rate constants, we have detected an optimal range that maximizes orientation bias in CF gradients. We have also examined different desensitization and receptor recycling mechanisms that yield experimentally documented orientation behavior. These yield novel insights into the relationship between receptor dynamics and leukocyte chemosensory movement behavior.
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    Bulletin of mathematical biology 56 (1994), S. 1143-1162 
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    Notes: Abstract Given two independent sequences of letters, we seek the probability distribution of the length of the longest matching word. This word can be in different positions in the two sequences and we consider both perfect and nearly perfect matching. We derive bounds and approximations for the probability and compare them with other bounds and approximations. The results can be applied to DNA sequences in molecular biology and generalized matching between two independent random sequences.
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    Bulletin of mathematical biology 56 (1994), S. 1163-1172 
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    Bulletin of mathematical biology 58 (1996), S. 43-63 
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    Notes: Abstract The parameter domain for which the quasi-steady state assumption is valid can be considerably extended merely by a simple change of variable. This is demonstrated for a variety of biologically significant examples taken from enzyme kinetics, immunology and ecology.
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    Bulletin of mathematical biology 58 (1996), S. 103-127 
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    Notes: Abstract The ability of random fluctuations in selection to maintain genetic diversity is greatly increased when generations overlap. This result has been derived previously using genetic models with very special assumptions about the population age structure. Here we explore its robustness in more realistic population models, with very general age structure or physiological structure. For a range of genetic models (haploid, diploid, single and multilocus) we find that the condition for maintaining genetic diversity generalizes almost without change. Genetic diversity is maintained by selection if a product of the form (generation overlap)×(selection intensity)×(variability in the selection regime) is sufficiently large, where the generation overlap is measured in units of Fisher's reproductive value. This conclusion is based on a local evolutionary stability analysis, which differs from the standard “protected polymorphism” criterion for the maintenance of genetic diversity. Simulation results match the predictions from the local stability analysis, but not those from the protected polymorphism criterion. The condition obtained here for maintaining genetic diversity requires fitness fluctuations that are substantial but well within the range observed in many studies of natural populations.
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    Bulletin of mathematical biology 58 (1996), S. 203-206 
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    Bulletin of mathematical biology 58 (1996), S. 265-283 
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    Notes: Abstract Premised on relatively simple assumptions, mathematical models like those of Monod, Pirt or Droop inadequately explain the complex transient behavior of microbial populations. In particular, these models fail to explain many aspects of the dynamics of aTetrahymena pyriformis-Escherichia coli community. In this study an alternative approach, an individual-based model, is employed to investigate the growth and interactions ofTetrahymena pyriformis andE. coli in a batch culture. Due to improved representation of physiological processes, the model provides a better agreement with experimental data of bacterial density and ciliate biomass than previous modeling studies. It predicts a much larger coexistence domain than rudimentary models, dependence of biomass dynamics on initial conditions (bacteria to ciliate biomasses ratio) and appropriate timing of minimal bacteria density. Moreover, it is found that accumulation ofE. coli sized particles andE. coli toxic metabolites has a stabilizing effect on the system.
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    Bulletin of mathematical biology 58 (1996), S. 313-365 
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    Notes: Abstract At the core of contemporarymorphometrics—the quantitative study of biological shape variation—is a synthesis of two originally divergent methodological styles. One contributory tradition is the multivariate analysis of covariance matrices originally developed as biometrics and now dominant across a broad expanse of applied statistics. This approach, couched solely in the linear geometry of covariance structures, ignores biomathematical aspects of the original measurements. The other tributary emphasizes the direct visualization of changes in biological form. However, making objective the biological meaning of the features seen in those diagrams was always problematical; also, the representation of variation, as distinct from pairwise difference, proved infeasible. To combine these two variants of biomathematical modeling into a valid praxis for quantitative studies of biological shape was a goal earnestly sought though most of this century. That goal was finally achieved in the 1980s when techniques from mathematical statistics, multivariate biometrics, non-Euclidean geometry and computer graphics were combined in a coherent new system of tools for the complete regionalized quantitative analysis oflandmark points together with the biomedical images in which they are seen. In this morphometric synthesis, correspondence of landmarks (biologically labeled geometric points, like “bridge of the nose”) across specimens is taken as a biomathematical primitive. The shapes of configurations of landmarks are defined as equivalence classes with respect to the Euclidean similarity group and then represented as single points in David Kendall'sshape space, a Riemannian manifold with Procrustes distance as metric. All conventional multivariate strategies carry over to the study of shape variation and covariation when shapes are interpreted in the tangent space to the shape manifold at an average shape. For biomathematical interpretation of such analyses, one needs a basis for the tangent space compatible with the reality of local biotheoretical processes and explanations at many different geometric scales, and one needs graphics for visualizing average shape differences and other statistical contrasts there. Both of these needs are managed by thethin-plate spline, a deformation function that has an unusually helpful linear algebra. The spline also links the biometrics of landmarks to deformation analysis of the images from which the landmarks originally arose. This article reviews the history and principal tools of this synthesis in their biomathematical and biometrical context and demonstrates their usefulness in a study of focal neuroanatomical anomalies in schizophrenia.
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    Bulletin of mathematical biology 58 (1996), S. 425-447 
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    Notes: Abstract A competition model describing tumor-normal cell interaction with the added effects of periodically pulsed chemotherapy is discussed. The model describes parameter conditions needed to prevent relapse following attempts to remove the tumor or tumor metastasis. The effects of resistant tumor subpopulations are also investigated and recurrence prevention strategies are explored.
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    Bulletin of mathematical biology 58 (1996), S. 409-424 
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    Notes: Abstract Increasing attention is being paid to the configuration and development of vascular structures and their possible correlations with physiological events. The study of angiogenesis in normal and pathological states as well as in the embryo and adult has provided new insights into the mechanism of vessel growth and organization of the vasculature. Various mathematical branching models have been developed. These constructions are mainly geometrical and only involve a branching phenomenon. We propose the use of a deterministic non-linear model based on physiological laws and hydrodynamics. Growth, branching and anastomosis, the three actual main events occurring in vascular growth, are included in this model. Space growth, including cells and vessels, is defined by a decreasing transformation. Space density and the length of new sprouts are controlled by a set of parameters. The conditions on these parameters are well established, which allows the production of realistic patterns.
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    Bulletin of mathematical biology 58 (1996), S. 555-568 
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    Notes: Abstract The quasi-stationary distribution of a population within a system of interacting populations is approximated by a stochastic logistic process. The parameters of this process can be expressed in the parameters of the full system. Using the diffusion approximation, an expression for the expected extinction time is derived from this logistic process. Since the expected extinction time is expressed in the parameters of the full system, the effect of these parameters on the extinction risk can be easily evaluated, which may be of use for studies in ecology, conservation biology and epidemiology. The outcome is compared with simulation results for the case of a prey-predator system.
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    Notes: Abstract The cytokines are the information superhighway of the immune system. They are an important component of the integrated behavior of the system. In order to be able to have a good understanding of the immune system, we must be able to model the effect of cytokines and their combined effect. This work is a step in that direction. We study the combined effect of two cytokines: interleukin-2 (IL-2) and interleukin-4 (IL-4) on some cells of the immune system. Interleukin-2 and interleukin-4 are important growth and differentiation factors for B and T cells. Interleukin-4 antagonizes the effect of interleukin-2 on B cells and some T cells while it synergizes with interleukin-2 on other T cells. We build a mathematical model of the interaction of both cytokines on T and B cells as a building block toward a model of the Th1/Th2 cross-regulation. The response of a given cell to the combination of interleukin-2 and interleukin-4 is shown to involve competing dynamical effects which can lead to either antagnostic or synergistic combined effect.
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    Bulletin of mathematical biology 58 (1996), S. 661-717 
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    Notes: Abstract We propose a mathematical approach to the modelling of self-organizing hierarchies in animal societies. This approach relies on a basic positive feedback mechanism that reinforces the ability of a given individual to win or to lose in a hierarchical interaction, depending on how many times it won or lost in previous interactions. Motivated by experiments carried out on primitively eusocial waspsPolistes, the model, is based on coupled differential equations supplemented with a small stochastic term. Numerical integrations allow many different hierarchical profiles to be obtained depending on the model parameters: (1) the particular form of the probability for an individual to win or lose a fight given its history, (2) the probability of interaction between two individuals, (3) the forgetting strength, which determines the rate at which events in the past are forgotten and no longer influence the force of an individual and (4) two individual recognition parameters, which set the contribution of individual recognition in the process of hierarchical genesis. We compare the results, expressed in terms of a hierarchical index or of the Landau number that describes the degree of linearity of the hierarchy, with various experimental results.
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    Bulletin of mathematical biology 58 (1996), S. 809-810 
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    Bulletin of mathematical biology 58 (1996), S. 787-808 
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    Notes: Abstract The normal process of dermal wound healing fails in some cases, due to fibro-proliferative disorders such as keloid and hypertrophic scars. These types of abnormal healing may be regarded as pathologically excessive responses to wounding in terms of fibroblastic cell profiles and their inflammatory growth-factor mediators. Biologically, these conditions are poorly understood and current medical treatments are thus unreliable. In this paper, the authors apply an existing deterministic mathematical model for fibroplasia and wound contraction in adult mammalian dermis (Olsenet al., J. theor. Biol. 177, 113–128, 1995) to investigate key clinical problems concerning these healing disorders. A caricature model is proposed which retains the fundamental cellular and chemical components of the full model, in order to analyse the spatiotemporal dynamics of the initiation, progression, cessation and regression of fibro-contractive diseases in relation to normal healing. This model accounts for fibroblastic cell migration, proliferation and death and growth-factor diffusion, production by cells and tissue removal/decay. Explicit results are obtained in terms of the model processes and parameters. The rate of cellular production of the chemical is shown to be critical to the development of a stable pathological state. Further, cessation and/or regression of the disease depend on appropriate spatiotemporally varying forms for this production rate, which can be understood in terms of the bistability of the normal dermal and pathological steady states—a central property of the model, which is evident from stability and bifurcation analyses. The work predicts novel, biologically realistic and testable pathogenic and control mechanisms, the understanding of which will lead toward more effective strategies for clinical therapy of fibro-proliferative disorders.
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    Bulletin of mathematical biology 58 (1996), S. 907-922 
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    Notes: Abstract Populations often exhibit abrupt changes in abundance associated with a smooth, continuous change in some component of their environment, with the abruptness usually attributed to inter-specific interactions or physical extremes. This paper presents a spatially explicit single-species population model in which intra-specific interactions alone are responsible for such an abrupt change. The essential mechanism involves cooperation in both colonization (through enhanced recruitment near other individuals) and mortality (protection through a “safety-in-numbers” interaction). Large fluctuations in population density would likely be observable near the transition region.
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    Bulletin of mathematical biology 58 (1996), S. 1019-1022 
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    Notes: Abstract A mathematical model of the nitrogen transformation cycle in an aquatic environment is studied. Using Pontryagin's maximum principle, a preferential utilization of ammonium to nitrate by phytoplankton is explained and verified by experimental data. A multiparameter bifurcation is given. The model was found to have four types of equilibrium sets. It is shown that a Hopf bifurcation may occur.
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    Bulletin of mathematical biology 58 (1996), S. 1075-1097 
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    Notes: Abstract Parallel computation employing a domain decomposition method was used to calculate precisely without approximations the spatio-temporal distribution of Ca2+ in nerve terminals. The results showed, contrary to expectations, that for equal admitted Ca2+ currents at low (one channel open) and high (four channels open) depolarization, the average Ca2+ concentration at the release area is higher at the low depolarization. These calculations provide additional support for the Ca2+-voltage hypothesis for neurotransmitter release.
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    Bulletin of mathematical biology 58 (1996), S. 1099-1121 
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    Notes: Abstract Type I hypersensitivity, which functions to protect the organism from parasites, is caused by binding of antigen to IgE antibodies pre-attached to the cell surface of tissue mast cells and their circulating counterparts, the basophils. In “allergy,” type I hypersensitivity is inappropriately induced by protein-based foreign substances (such as pollen) or protein components of insect stings, which in the normal course of events would be cleared from the organism without causing any damage. Paradoxically, a successful clinical treatment of allergy involves repeated immunization of allergic persons with low doses of the allergen—immunotherapy. Investigation of the available experimental evidence leads to the conclusion that the phenomena of immunotherapy are best addressed in terms of the interplay among the mechanism(s) of immune memory—Th1/Th2 cross-regulation—and the physical compart-mentalization of the immune system. These conclusions are illustrated with a numerical simulation.
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    Bulletin of mathematical biology 59 (1997), S. 23-41 
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    Notes: Abstract We consider a host-solitary parasitoid system with three categories of individuals: parasitoids, healthy hosts and parasitized hosts. Parasitoids are assumed to discriminate perfectly between the two kinds of hosts and they can reject those which are already parasitized. If parasitoids systematically accept or reject superparasitism or behave randomly, the system is always unstable. Using an optimal foraging model, we determine the behavior of parasitoids which leads to maximization of the instantaneous reproductive rate. When following this adaptive decision rule, parasitoids accept or refuse superparasitism according to the densities of both healthy and parasitized hosts. We study the dynamics of the system when parasitoids follow the optimal rule and show that under certain conditions it possesses a locally stable equilibrium point. In addition, our model predicts that at equilibrium parasitoids show partial preferences for superparasitism.
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    Bulletin of mathematical biology 59 (1997), S. 205-232 
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    Notes: Abstract A system of differential equations for the control of tumor growth cells in a cycle nonspecific chemotherapy is analyzed. Spontaneously acquired drug resistance is taken into account, and a criterion for the selection of chemotherapeutic treatment is used. This criterion purports to describe the possibility of improvement of the patient's health when treatment is discontinued. Contrary to our early results which also take drug resistance into account, in this context strategies of continuous chemotherapy in which rest periods take part may be better than maximum drug concentration throughout the treatment (which appears to be in accordance with clinical practice). This bears out our previous conjecture that when drug resistance is accounted for, the imperfections in the usual modelling of treatment criteria, which in general do not allow for patient recuperation, ruled out the possibility of rest periods in optimal continuous chemotherapy.
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    Bulletin of mathematical biology 59 (1997), S. 255-262 
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    Notes: Abstract A logistic density-dependent matrix model is developed in which the matrices contain only parameters and recruitment is a function of adult population density. The model was applied to simulate introductions of white-tailed deer into an area; the fitted model predicted a carrying capacity of 215 deer, which was close to the observed carrying capacity of 220 deer. The rate of population increase depends on the dominant eigenvalue of the Leslie matrix, and the age structure of the simulated population approaches a stable age distribution at the carrying capacity, which was similar to that generated by the Leslie matrix. The logistic equation has been applied to study many phenomena, and the matrix model can be applied to these same processes. For example, random variation can be added to life history parameters, and population abundances generated with random effects on fecundity show both the affect of annual variation in fecundity and a longer-term pattern resulting from the age structure.
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    Bulletin of mathematical biology 59 (1997), S. 399-406 
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    Bulletin of mathematical biology 58 (1996), S. 835-859 
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    Notes: Abstract In the presence of seasonal forcing, predator-prey models with quadratic interaction terms and weak dissipation can exhibit infinite numbers of coexisting periodic attractors corresponding to cycles of different magnitude and frequency. These motions are best understood with reference to the conservative case, for which the degree of dissipation is, by definition, zero. Here one observes the familiar mix of “regular” (neutrally stable orbits and tori) and chaotic motion typical of non-integrable Hamiltonian systems. Perturbing away from the conservative limit, the chaos becomes transitory. In addition, the invariant tori are destroyed and the neutrally stable periodic orbits becomes stable limit cycles, the basins of attraction of which are intertwined in a complicated fashion. As a result, stochastic perturbations can bounce the system from one basin to another with consequent changes in system behavior. Biologically, weak dissipation corresponds to the case in which predators are able to regulate the density of their prey well below carrying capacity.
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    Bulletin of mathematical biology 58 (1996), S. 923-938 
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    Notes: Abstract The standard method for measuringin vitro antibiotic efficacy is based on a point observation of bacterial activity 18 hours after inoculation. The method, while simple, forgoes significant information by ignoring the dynamics of the interations between antibiotic and bacteria. This paper proposes a simple dynamic model describing these interactions. The model consists of two non-linear differential equations of the S-system type. Its parameter values are estimated, through the minimization of residual errors, from data on the effect of the carbapenem antibiotic imipenem onPseudomonas aeruginosa. The model adequately describes the dynamic behavior of the bacterial populations in the presence of the antibiotic: beginning with drug administration, then through the decline of the bacterial population and possibly ending with bacterial resurgence.
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    Bulletin of mathematical biology 58 (1996), S. 1001-1018 
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    Notes: Abstract We have studied an ecological system of two species, which we denotestrong andweak, respectively, that compete for a single food resource. This system is modelled as a three component reaction-diffusion process. In the presence of a solitary pulse of increased resources, the weaker competitor can diffuse toward this surplus, gaining a competitive advantage and hence persisting in contraposition with the classical Lotka-Volterra result. An exact analytical solution has been found through a quantum mechanical analogy. A stability analysis of this solution against changes in different parameters has been carried out.
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    Bulletin of mathematical biology 58 (1996), S. 1023-1046 
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    Notes: Abstract Collapsible-tube flow with self-excited oscillations has been extensively investigated. Though physiologically relevant, forced oscillation coupled with self-excited oscillation has received little attention in this context. Based on an ODE model of collapsible-tube flow, the present study applies modern dynamics methods to investigate numerically the responses of forced oscillation to a limit-cycle oscillation which has topological characteristics discovered in previous unforced experiments. A devil's staircase and period-doubling cascades are presented with forcing frequency and amplitude as control parameters. In both cases, details are provided in a bifurcation diagram. Poincaré sections, a frequency spectrum and the largest Lyapunov exponents verify the existence of chaos in some circumstances. The thin fractal structure found in the strange attractors is believed to be a result of high damping and low stiffness in such systems.
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    Bulletin of mathematical biology 58 (1996), S. 1155-1170 
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    Notes: Abstract In this work, we show that a one-dimensional model of the blood flow across the lungs can reproduce the evolution of a bolus versus the time. Solving the differential equation governing the bolus concentration in the framework of this model, we determine the solution which fulfills Gaussian initial boundary conditions. An effective parameter related to the ratio of a diffusion coefficient to the square of the mean speed of the flow is defined. The determination of its numerical values following a semi-empirical approach enables us to know accurately the mean transit time and the cardiac output. The results have been compared to other methods, and were found in good agreement. Such an approach could be of interest in all studies where the knowledge of flow—including micro-circulation—is needed.
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    Bulletin of mathematical biology 58 (1996), S. 1187-1207 
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    Notes: Abstract How two species interact during and after colonization influences which of them will be present in each stage of succession. In the tolerance model of ecological succession in a patchy environment, empty patches can be colonized by any species, but the ability to tolerate reduced resource levels determines which species will exclude the other. Here, we analyze a meta-population model of the possible roles of competition in colonization and succession, using non-linear Markov chains as a mathematical framework. Different kinds of competition affect the final equilibrial, abundances of the species involved in qualitatively different ways. An explicit criterion is given to determine which interactions have stronger effects on the final equilibrial levels of the weaker, species. Precise conditions are stated for the co-existence of both species. Both species are more likely to co-exist in the presence of an intermediate disturbance frequency.
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    Bulletin of mathematical biology 59 (1997), S. 707-724 
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    Notes: Abstract A system of differential equations for the control of tumor cells growth in a cycle nonspecific chemotherapy is presented. Spontaneously acquired drug resistance is accounted for, as well as the evolution in time of normal cells. In addition, optimization of conflicting objectives forms the aim of the chemotherapeutic treatment. For general cell growth, some results are given, whereas for the special case of Malthusian (exponential) growth of tumor cells and rather general growth rate for normal cells, the optimal strategy is worked out. The latter, from the clinical standpoint, corresponds to maximum drug concentration throughout the treatment.
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    Bulletin of mathematical biology 59 (1997), S. 787-807 
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    Bulletin of mathematical biology 59 (1997), S. 809-831 
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    Notes: Abstract This study examines the influence of various host-feeding patterns on host-parasitoid population dynamics. The following types of host-feeding patterns are considered: concurrent and non-destructive, non-concurrent and non-destructive, and non-concurrent and destructive. The host-parasitoid population dynamics is described by the Lotka-Volterra continuous-time model. This study shows that when parasitoids behave optimally, i.e. they maximize their fitness measured by the instantaneous per capita growth rate, the non-destructive type of host feeding stabilizes host-parasitoid dynamics. Other types of host feeding, i.e. destructive, concurrent, or non-concurrent, do not qualitatively change the neutral stability of the Lotka-Volterra model. Moreover, it is shown that the pattern of host feeding which maximizes parasitoid fitness is either non-concurrent and destructive, or concurrent and non-destructive host feeding, depending on the host abundance and parameters of the model. The effects of the adaptive choice of host-feeding patterns on host-parasitoid population dynamics are discussed.
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    Bulletin of mathematical biology 59 (1997), S. 931-952 
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    Notes: Abstract Game theory has had remarkable success as a framework for the discussion of animal behaviour and evolution. It suggested new interpretations and prompted new observational studies. Most of this work has been done with 2-player games. That is the individuals of a population compete in pairwise interactions. While this is often the case in nature, it is not exclusively so. Here we introduce a class of models for situations in which more than two (possibly very many) individuals compete simultaneously. It is shown that the solutions (i.e. the behaviour which may be expected to be observable for long periods) are more complex than for 2-player games. The concluding section lists some of the new phenomena which can occur.
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    Notes: Abstract A method allowing to measure the inhomogeneous distribution of purines/pyrimidines in nucleotide sequences is developed. We show that this measure relates to the coding or non-coding character of the considered sequence. Coding sequences present a near to the random Pu or Py distribution. This property is shared by both protein-coding DNA and functional RNA-coding DNA. Non-coding sequences present a highly clustered inhomogeneity. We propose the hypothesis, corroborated with appropriate computer simulations, that this is due to the action of various transposition events accumulated for long time periods.
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    Bulletin of mathematical biology 59 (1997), S. 1047-1075 
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    Notes: Abstract The potential generated in the smooth muscle of the vas deferens on release of a quantum of transmitter from a varicosity was analyzed using a three-dimensional bidomain continuum model. Current was injected at the origin of the bidomain; this current had the temporal characteristics of the junctional current. The membrane potential, intracellular potential, and extracellular potential, as well as the extracellular current, were then calculated throughout the bidomain at different times. Calculations were performed to show the effect of changing the anisotropy ratios of the intracellular and extracellular conductivities on the spread of current and potential in each of the three dimensions. These results provide a theoretical framework for ascertaining the time course of transmitter interaction at a varicosity following the secretion of a quantum of transmitter.
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    Bulletin of mathematical biology 59 (1997), S. 1145-1154 
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    Notes: Abstract Parabolic growth invariably results in the survival of all competing types. Under the constraint of constant total concentration, there is a unique equilibrium in the simplex interior, which is asymptotically stable inside the whole simplex. The appropriate Lyapunov function is obtained in terms of the excess productivity which is shown to be maximized for the competitive system with fractional order kinetics. Claims to the contrary are refuted.
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    Bulletin of mathematical biology 59 (1997), S. 1191-1201 
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    Bulletin of mathematical biology 59 (1997), S. 763-785 
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    Notes: Abstract The purpose of this study was to investigate strategies in the monotherapy treatment of HIV infection in the presence of drug-resistant (mutant) strains. A mathematical system is developed to model resistance in HIV chemotherapy. It includes the key players in the immune response to HIV infection: virus and both uninfected CD4+ and infected CD4+ T-cell populations. We model the latent and progressive stages of the disease, and then introduce monotherapy treatment. The model is a system of differential equations describing the interaction of two distinct classes of HIV—drug-sensitive (wild type) and drug-resistant (mutant)—with lymphocytes in the peripheral blood. We then introduce chemotherapy effects. In the absence of treatment, the model produces the three types of qualitative clinical behavior—anuninfected steady state, andinfected steady state (latency), andprogression to AIDS. Simulation of treatment is provided for monotherapy, during theprogression to AIDS state, in the consideration of resistance effects. Treatment benefit is based on an increase or retention in CD4+ T-cell counts together with a low viral titer. We explore the following treatment approaches: an antiviral drug which reduces viral infectivity that is administered early—when the CD4+ T-cell count is ≥300/mm3, and late—when the CD4+ T-cell count is less than 300/mm3. We compare all results with data. When treatment is initiated during the progression to AIDS state, treatment prevents T-cell collapse, but gradually loses effectiveness due to drug resistance. We hypothesize that it is the careful balance of mutant and wild-type HIV strains which provides the greatest prolonged benefit from treatment. This is best achieved when treatment is initiated when the CD4+ T-cell counts are greater than 250/mm3, but less than 400/mm3 in this model (i.e. not too early, not too late). These results are supported by clinical data. The work is novel in that it is the first model to accurately simultate data before, during and after monotherapy treatment. Our model also provides insight into recent clinical results, as well as suggests plausible guidelines for clinical testing in the monotherapy of HIV infection.
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    Bulletin of mathematical biology 59 (1997), S. 833-856 
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    Notes: Abstract A mathematical model which describes adhesion of bacteria to host cell lines is presented. The model is flexible enough to account for the following situations: extracellular bacteria are either in exponential or in stationary phase. Adhesion is described as a reversible binding process in which the bacteria attach to or detach from specific receptors uniformly distributed on the cell surface. In turn, attached bacteria can either replicate or, conversely, they are restrained to remain in stationary phase. In the first case, however, we must consider the problem of whether the decrease of unoccupied receptors as adhesion progresses imposes a limit to the replicating capacity of the attached bacteria. The effect exerted by the multiplicity of infection (MOI), i.e. the ratio of the number of bacteria to the number of host cells, on the process of adhesion is also contemplated by the model. This has revealed that experiments performed at the same values of MOI can show completely different levels of adhered bacteria, depending on the number of host cells in the assays. This finding demonstrates that the report of the MOI values is insufficient to characterize comparative studies of bacterial adhesion since it could lead to a misunderstanding of the corresponding data. Simplified models based on the steady-state approximation and in equilibrium analysis by means of a Lagmuir adsorption isotherm for the attached bacteria are also discussed. This allows us to define the adhesion coefficient (β) in a given bacterium-cell system so that, with the exception of those systems where these coefficients cannot be defined, larger values of β are related to a greater adhesion capacity. An overview of the procedures to perform quantitative adhesion data analysis is outlined. Finally, theoretical predictions are compared with experimental results from the literature.
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    Bulletin of mathematical biology 59 (1997), S. 897-910 
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    Notes: Abstract A new measure of toxicity based on stochastic modelling of single photon-counting processes, representing time-resolved phagocyte luminescence of xenobiotic-perturbed human neutrophils, has been constructed. The stochastic measure of toxicity has been verified by the QSAR method, and then compared and contrasted with the traditional toxicity measure used in bio- and chemiluminescent research. Phenol and benzene homologues were chosen as perturbers due to their importance from the viewpoint of ecotoxicology and occupational medicine.
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    Bulletin of mathematical biology 59 (1997), S. 953-973 
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    Notes: Abstract We describe a mathematical model of the flow and deformation in a human teat. Our aim is to compare the theoretical milk yield during infant breast feeding with that obtained through the use of a breast pump. Infants use a peristaltic motion of the tongue, along with some suction, to extract milk, whereas breast pumps use a cyclic pattern of suction only. Our model is based on quasi-linear poroelasticity whereby the teat is modelled as a cylindrical porous elastic material saturated with fluid. We impose a cyclic axial suction pressure difference across the teat and impose a radial compressive force moving along the teat which mimics infant suckling. This is compared to the case of cyclic and steady pumping only which models the action of breast pumps. The results illustrate that there is an optimal time to apply the compressive force during the suction cycle that will increase the flow rate in our theoretical teat. The model and results may be of use in the future design of effective breast pumps.
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    Bulletin of mathematical biology 59 (1997), S. 993-1012 
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    Notes: Abstract In the present work, we study the propagation of solitary waves in a prestressed thick walled elastic tube filled with an incompressible inviscid fluid. In order to include the geometric dispersion in the analysis the wall inertia and shear deformation effects are taken into account for the inner pressure-cross-sectional area relation. Using the reductive perturbation technique, the propagation of weakly non-linear waves in the long-wave approximation is examined. It is shown that, contrary to thin tube theories, the present approach makes it possible to have solitary waves even for a Mooney-Rivlin (M-R) material. Due to dependence of the coefficients of the governing Korteweg-deVries equation on initial deformation, the solution profile changes with inner pressure and the axial stretch. The variation of wave profiles for a class of elastic materals are depicted in graphical forms. As might be seen from these illustrations, with increasing thickness ratio, the profile of solitary wave is steepened for a M-R material but it is broadened for biological tissues.
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    Bulletin of mathematical biology 59 (1997), S. 1077-1100 
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    Notes: Abstract Adult dermal wounds, in contrast to fetal wounds, heal with the formation of scar tissue. A crucial factor in determining the degree of scarring is the ratio of types I and III collagen, which regulates the diameter of the combined fibers. We developed a reaction-diffusion model which focuses on the control of collagen synthesis by different isoforms of the polypeptide transforming growth factor-β (TGFβ). We used the model to investigate the current controversy as to whether the fibroblasts migrate into the wound from the surrounding unwounded dermis or from the underlying subcutaneous tissue. Numerical simulations of a spatially independent, temporal model led to a value of the collagen ratio consistent with that of healthy tissue for the fetus, but corresponding to scarring in the adult. We investigated the effect of topical application of TGFβ and show that addition of isoform 3 reduces scar tissue formation, in agreement with the experiment. However, numerical solutions of the reaction-diffusion system do not exhibit this sensitivity to growth factor application. Mathematically, this corresponds to the observation that behind healing wavefront solutions, a particular healed state is always selected independent of transients, even though there is a continuum of possible positive steady states. We explain this phenomenon using a caricature system of equations, which reflects the key qualitative features of the full model but has a much simpler mathematical form. Biologically, our results suggest that the migration into a wound of fibroblasts and TGFβ from the surrounding dermis alone cannot account for the essential features of the healing process, and that fibroblasts entering from the underlying subcutaneous tissue are crucial to the healing process.
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    Bulletin of mathematical biology 59 (1997), S. 1125-1144 
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    Notes: Abstract Oscillations in cytosolic Ca2+ concentrations in living cells are often a manifestation of propagating waves of Ca2+. Numerical simulations with a realistic model of inositol 1, 4, 5-trisphosphate (IP3)-induced Ca2+ wave trains lead to wave speeds that increase linearly at long times when (a) IP3 levels are in the range for Ca2+ oscillations, (b) a gradient of phase is established by either an initial ramp or pulse of IP3, and (c) IP3 concentrations asymptotically become uniform. We explore this phenomenon with analytical and numerical methods using a simple two-variable reduction of the De Young-Keizer model of the IP3 receptor that includes the influence of Ca2+ buffers. For concentrations of IP3 in the oscillatory regime, numerical solution of the resulting reaction diffusion equations produces nonlinear wave trains that shows the same asymptotic growth of wave speed. Due to buffering, diffusion of Ca2+ is quite slow and, as previously noted, these waves occur without appreciable bulk movement of Ca2+. Thus, following Neu and Murray, we explore the behavior of these waves using an asymptotic expansion based on the small size of the buffered diffusion constant for Ca2+. We find that the gradient in phase of the wave obeys Burgers' equation asymptotically in time. This result is used to explain the linear increase of the wave speed observed in the simulations.
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    Bulletin of mathematical biology 59 (1997), S. 1183-1189 
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    Notes: Abstract The robustness of patterning events in development is a key feature that must be accounted for in proposed models of these events. When considering explicitly cellular systems, robustness can be exhibited at different levels of organization. Consideration of two widespread patterning mechanisms suggests that robustness at the level of cell communities can result from variable development at the level of individual cells; models of these mechanisms show how interactions between participating cells guarantee community-level robustness. Cooperative interactions enhance homogeneity within communities of like cells and the sharpness of boundaries between communities of distinct cells, while competitive interactions amplify small inhomogeneities within communities of initially equivalent cells, resulting in fine-grained patterns of cell specialization.
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    Circuits, systems and signal processing 13 (1994), S. 273-293 
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    Notes: Abstract A basic control engineer's adage-the poles of a feedback compensator become zeros of the closed-loop system-admits difficulties of interpretation even in the most simple of cases; that of single-input, single-output. An earlier investigation has provided an analysis of this adage in a module-theoretic context for systems in state space form while avoiding restrictive assumptions on system minimality or squareness. The main result is expressed concisely in terms of an exact sequence of modules which include Ω-zero modules corresponding to the feedback system and the plant. Extended zero modules of Ω-type incorporate both finite invariant zero structure, and generic zero information which occurs when a system fails to be right-invertible. In the case of compensation in the feedback path, this main exact sequence reduces to a mathematically clear expression of the aforementioned adage: the Ω-zero module of the feedback system is precisely the direct sum of the Ω-zero module of the plant and the system pole module of the feedback compensator. This paper extends the previous work in order to avoid assumptions on causality in the plant. Implicit dynamical systems are employed, in lieu of systems in state space form. Once again, it is not assumed that the system is one-to-one or onto; and so the concepts of generic zeros and their modules are brought into the arena of implicit systems. The implicit system itself is assumed in this work to be regular; however, decoupling zeros are permitted. Moreover, input-decoupling zeros and system pole feedback relationships are considered.
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    Circuits, systems and signal processing 13 (1994), S. 387-388 
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    Circuits, systems and signal processing 13 (1994), S. 373-384 
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    Notes: Abstract When the problem is considered of obtaining a periodic description in state-space form of a linear process which can be modelled by linear difference equations with periodic coefficients, it is natural to ask whether it is possible to preliminarily derive a polynomial equivalent form of such equations, which in the periodic case plays a role similar to the Rosenbrock's polynomial matrix description of a linear time-invariant process. In this paper a polynomial time-invariant description of a linear periodic process is introduced. It is shown that such a polynomial description gives a simple characterization of the dimension of the space of the solutions corresponding to the null input function, i.e., of the order of the periodic model under consideration. In addition, it allows us to introduce a transfer matrix for the computation of the output responses corresponding to null initial conditions, and to deduce conditions for the periodic model to be causal. These results, as well as the possibility of defining strict system equivalence between two periodic models through their time-invariant polynomial descriptions, in a similar sense as in the time-invariant case, show the relevance of such a polynomial time-invariant description for the problem under consideration.
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    Circuits, systems and signal processing 13 (1994), S. 435-453 
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    Notes: Abstract An actual sampling process can be modeled as a random process, which consists of the regular (uniform) deterministic sampling process plus an error in the sampling times which constitutes a zero-mean noise (the jitter). In this paper we discuss the problem of estimating the jitter process. By assuming that the jitter process is an i.i.d. one, with standard deviation that is small compared to the regular sampling time, we show that the variance of the jitter process can be estimated from thenth order spectrum of the sampled data,n=2, 3, i.e., the jitter variance can be extracted from the 2nd-order spectrum or the 3rd-order spectrum (the bispectrum) of the sampled data, provided the continuous signal spectrum is known. However when the signal skewness exceeds a certain level, the potential performance of the bispectrum-based estimation is better than that of the spectrum-based estimation. Moreover, the former can also provide jitter variance estimates when the continuous signal spectrum is unknown while the latter cannot. This suggests that the bispectrum of the sampled data is potentially better for estimating any parameter of the sampling jitter process, once the signal skewness is sufficiently large.
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    Circuits, systems and signal processing 15 (1996), S. 555-572 
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    Notes: Abstract This work addresses the design of LoG filters in the frequency domain within a structure formed by the cascade of quasi-Gaussian and discrete Laplacian filters. The main feature of such a structure is that it requires half the number of convolutions of the classical structure in which the LoG transfer function is expressed as the sum of two separable transfer functions of 1-D Gaussian and LoG type. Such a perspective allows one to rephrase the design of IIR and FIR filters for edge detection as a frequency domain approximation problem solvable by standard digital filter design tools. The zero-phase IIR solutions have a good performance at low orders and approximation errors practically independent of the aperture parameter. The characteristics of the nearly linear-phase IIR filters solving the problem suggest the consideration of linear-phase FIR filters with zeros constrained on the unit circle. The use of such filters leads to remarkable computational savings with respect to the filters designed by impulse response sampling. The agreement between the edge values obtained by the filters designed according to the scheme proposed in this work and those obtained by standard techniques is very good.
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    The journal of Fourier analysis and applications 1 (1994), S. 67-85 
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    Notes: Abstract Functions belonging to various Paley-Wiener spaces have representations in sampling series. When a function does not belong to such a space, the sampling series may converge, not to the object function but to an "alias" of it, and an aliasing error is said to occur. Aliasing error bounds are derived for one- and two-channel sampling series analogous to the Whittaker-Kotel’nikov-Shannon series, and for the multi-band sampling series, and a "derivative" extension of it, due to Dodson, Beaty, et al. The Poisson summation formula is a basic tool throughout. Aliasing in the one-channel case is shown to arise from a transformation with similarities to a projection. Where possible, the sharpness of the error bounds is discussed.
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    The journal of Fourier analysis and applications 1 (1994), S. 113-130 
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    Notes: Abstract This paper is devoted to a study of the Hausdorff-Young theorems from a historical perspective, beginning with the F. Riesz-Fischer theorem. Introduced by W. H. Young (1912), these theorems were considered and extended by F. Hausdorff (1923), F. Riesz (1923), E.C. Titchmarsh (1924), G. H. Hardy and J.E. Littlewood (1926), M. Riesz (1927), and O. Thorin (1939/48). Special emphasis is placed upon the development of the proofs of the two Hausdorff-Young inequalities and their impact upon Fourier analysis as a whole, in particular on the M. Riesz-Thorin convexity theoremand on the interpolation of operators. The golden thread connecting the various extensions and generalizations is the concept of logarithmic convexity, one that goes back to the work of J. Hadamard (1896), A. Liapounoff (1901), J.L.W.V. Jensen (1906), and O. Blumenthal (1907).
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    The journal of Fourier analysis and applications 1 (1994), S. 171-191 
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    Notes: Abstract In this paper we give a further investigation of the method introduced by the author in [1, Frequency-domain bounds for nonnegative unsharply band-limited functions] for proving bounds for functions with nonnegative Fourier transforms. We also dealt with the question of how large the supremum KS of all numbers |f(u)| is with f the Fourier transform of a nonnegative integrable function F and f(0) = 1, |f(ku)| ≤ ε for k ∈ S. Here u 〉 0 and S ⊂ {2, 3, . . .}. This problem was related in [1] to finding the infimum MS of all numbers Mh = maxϑ [(1−h(ϑ))/(1− cos ϑ)] over all 2π-periodic even, smooth functions h whose Fourier cosine coefficients ak vanish for k ∉ S, and it was proved and announced for several cases that MS (1−KS ) = 1. In this paper we prove the results announced in [1]. To that end we generalize the method given in [1] to include Fourier transforms f of probability measures on R and a certain generalized function h, and we show that the numbers KS, MS are assumed as |f(u)|, Mh for certain allowed f,h. Moreover, we establish a fundamental relation between finding the numbers KS, MS and the numbers KT, MT where T = {2, 3, . . .}\S. In particular, we show that MT = 2KS (2KS − 1)−1,KT = 1/2 MS(MS − 1)−1 and that MT (1 − KT) = 1,KSKT = 1/2 , whenever MS (1 − KS) = 1.
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    The journal of Fourier analysis and applications 1 (1994), S. 281-295 
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    Notes: Abstract Finite energy band-limited functions are reconstructed iteratively from nonuniform sample values of the functions and its derivatives. It is shown that the maximum gap allowed between the sampling points increases linearly with the number of derivatives considered. Moreover, a more precise result is presented for the first derivative case and another reconstruction of the functions using the frame algorithm is deduced.
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    The journal of Fourier analysis and applications 1 (1994), S. 233-247 
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    Notes: Abstract In the early 1960s research into radar signal synthesis produced important formulas describing the action of the two-dimensional Fourier transform on auto- and crossambiguity surfaces. When coupled with the Poisson Summation formula, these results become applicable to the theory of Weyl-Heisenberg systems, in the form of lattice sum formulas that relate the energy of the discrete crossambiguity function of two signals f and g over a lattice with the inner product of the discrete autoambiguity functions of f and g over a "complementary" lattice. These lattice sum formulas provide a framework for a new proof of a result of N.J. Munch characterizing tight frames and for establishing an important relationship between l1-summability (condition A) of the discrete ambiguity function of g over a lattice and properties of the Weyl-Heisenberg system of g over the complementary lattice. This condition leads to formulas for upper frame bounds that appear simpler than those previously published and provide guidance in choosing lattice parameters that yield the most snug frame at a stipulated density of basis functions.
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    The journal of Fourier analysis and applications 1 (1994), S. 403-436 
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    Notes: Abstract Let $a〉0, b〉0, ab〈1;$ and let $g\in L^2({\Bbb R}).$ In this paper we investigate the relation between the frame operator $S:f\in L^2({\Bbb R})\rightarrow \sum_{n,m}\,(f,g_{na,mb})\,g_{na,mb}$ and the matrix $H$ whose entries $H_{k,l\,;\,k',l'}$ are given by $(g_{k'/b,l'/a},g_{k/b,l/a})$ for $k,l,k',l'\in{\Bbb Z}.$ Here $f_{x,y}(t)={\rm exp}(2\pi iyt)\,f(t-x),$ $t\in{\Bbb R}$ , for any $f\in L^2({\Bbb R}).$ We show that $S$ is bounded as a mapping of $L^2({\Bbb R})$ into $L^2({\Bbb R})$ if and only if $H$ is bounded as a mapping of $l^2({\Bbb Z}^2)$ into $l^2({\Bbb Z}^2).$ Also we show that $AI\leq S\leq BI$ if and only if $AI\leq\frac{1}{ab}\,H\leq BI,$ where $I$ denotes the identity operator of $L^2({\Bbb R})$ and $l^2({\Bbb Z}^2),$ respectively, and $A\geq 0,$ $B〈\infty.$ Next, when $g$ generates a frame, we have that $(g_{k/b,l/a})_{k,l}$ has an upper frame bound, and the minimal dual function $^{\circ}\gamma$ can be computed as $ab\,\sum_{k,l}\,(H^{-1})_{k,l\,;\,o,o}\,g_{k/b,l/a}.$ The results of this paper extend, generalize, and rigourize results of Wexler and Raz and of Qian, D. Chen, K. Chen, and Li on the computation of dual functions for finite, discrete-time Gabor expansions to the infinite, continuous-time case. Furthermore, we present a framework in which one can show that certain smoothness and decay properties of a $g$ generating a frame are inherited by $^{\circ}\gamma.$ In particular, we show that $^{\circ}\gamma\in{\cal S}$ when $g\in{\cal S}$ generates a frame $({\cal S}$ Schwartz space). The proofs of the main results of this paper rely heavily on a technique introduced by Tolimieri and Orr for relating frame bound questions on complementary lattices by means of the Poisson summation formula.
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    The journal of Fourier analysis and applications 1 (1994), S. 103-112 
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    Notes: Abstract For any ε 〉 0, we construct an orthonormal Schauder basis of C(K) consisting of trigonometric polynomials Tn n = 1, 2, . . . , such that deg(Tn) ≤ (1/2)(1 + ε)n. This is best possible with regard to the degree. The construction uses wavelet techniques.
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    The journal of Fourier analysis and applications 1 (1994), S. 131-170 
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    Notes: Abstract We study the general question of the existence of self-similar lattice tilings of Euclidean space. A necessary and sufficient geometric condition on the growth of the boundary of approximate tiles is reduced to a problem in Fourier analysis that is shown to have an elegant simple solution in dimension one. In dimension two we further prove the existence of connected self-similar lattice tilings for parabolic and elliptic dilations. These results apply to produce Haar wavelet bases and certain canonical number systems.
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    The journal of Fourier analysis and applications 1 (1994), S. 201-232 
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    Notes: Abstract In the spirit of work of Kerman and Sawyer, a condition is given that is necessary and sufficient for the Fourier transform norm inequality $\Big(\int_{{\Bbb R}_d} \vert\hat{f}\vert^q d\mu\Big)^{1/q} \leq C\Big(\int_{{\Bbb R}_d} \vert f\vert^p v\Big)^{1/p}$ provided v is a radial weight for which v−1/p is convexly decreasing and μ is a suitable measure. We also establish alternative conditions for such inequalities by proving corresponding trace type inequalities and maximal function inequalities that underlie the Fourier transform estimates. Our conditions are relatively simple to compute. Among applications we give extensions of a Sobolev restriction theorem.
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    The journal of Fourier analysis and applications 1 (1994), S. 297-310 
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    Notes: Abstract We present two-sided singular value estimates for a class of convolution-product operators related to time-frequency localization.
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    The journal of Fourier analysis and applications 3 (1996), S. 131-192 
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    Notes: Abstract We study boundary value problems for the time-harmonic form of the Maxwell equations, as well as for other related systems of equations, on arbitrary Lipschitz domains in the three-dimensional Euclidean space. The main goal is to develop the corresponding theory for Lp-integrable bounday data for optimal values of p's. We also discuss a number of relevant applications in electromagnetic scattering.
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    The journal of Fourier analysis and applications 3 (1996), S. 103-129 
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    Notes: Abstract Beurling's algebra $A^*=\{f:\sum_{k=0}^{\infty} \sup_{k\le |m|} |\hat f (m)| 〈 \infty \}$ is considered. A* arises quite naturally in problems of summability of the Fourier series at Lebesgue points, whereas Wiener's algebra A of functions with absolutely convergent Fourier series arises when studying the norm convergence of linear means. Certainly, both algebras are used in some other areas. A* has many properties similar to those of A, but there are certain essential distinctions. A* is a regular Banach algebra, its space of maximal ideals coincides with $[-\pi,\pi],$ and its dual space is indicated. Analogs of Herz's and Wiener-Ditkin's theorems hold. Quantitative parameters in an analog of the Beurling-Pollard theorem differ from those for A. Several inclusion results comparing the algebra A* with certain Banach spaces of smooth functions are given. Some special properties of the analogous space for Fourier transforms on the real axis are presented. The paper ends with a summary of some open problems.
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    The journal of Fourier analysis and applications 3 (1996), S. 193-205 
    ISSN: 1531-5851
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract We construct an algebra of left-invariant pseudodifferential operators on SU(2). We require only that the symbols be homogeneous and C2. For Fourier-bandlimited symbols, we derive the expected formulae for composition and commutators and construct an orthonormal basis of common approximate eigenvectors that could be used to study spectral theory. Some remarks on applications to matrices of operators are made.
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    Transformation groups 2 (1997), S. 225-267 
    ISSN: 1531-586X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract We study Edidin and Graham's equivariant Chow groups in the case of torus actions. Our main results are: (i) a presentation of equivariant Chow groups in terms of invariant cycles, which shows how to recover usual Chow groups from equivariant ones; (ii) a precise form of the localization theorem for torus actions on projective, nonsingular varieties; (iii) a construction of equivariant multiplicities, as functionals on equivariant Chow groups; (iv) a construction of the action of operators of divided differences on theT-equivariant Chow group of any scheme with an action of a reductive group with maximal torusT. We apply these results to intersection theory on varieties with group actions, especially to Schubert calculus and its generalizations. In particular, we obtain a presentation of the Chow ring of any smooth, projective spherical variety.
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    Transformation groups 2 (1997), S. 375-390 
    ISSN: 1531-586X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract In this paper we explicitly determine the virtual representations of the finite Weyl subgroups of the affine Weyl group on the cohomology of the space of affine flags containing a family of elementsn t in an affine Lie algebra. We also compute the Euler characteristic of the space of partial flags containingn t and give a connection with hyperplane arrangements.
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  • 93
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    Transformation groups 2 (1997), S. 351-374 
    ISSN: 1531-586X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mathematics
    Notes: Abstract LetG be a connected, simply-connected, real semisimple Lie group andK a maximal compactly embedded subgroup ofG such thatD=G/K is a hermitian symmetric space. Consider the principal fiber bundleM=G/K s →G/K, whereK s is the semisimple part ofK=K s ·Z K 0 andZ K 0 is the connected center ofK. The natural action ofG onM extends to an action ofG 1=G×Z K 0 . We prove as the main result thatM is weakly symmetric with respect toG 1 and complex conjugation. In the case whereD is an irreducible classical bounded symmetric domain andG is a classical matrix Lie group under a suitable quotient, we provide an explicit construction ofM=D×S 1 and determine a one-parameter family of Riemannian metrics Ω onM invariant underG 1. Furthermore,M is irreducible with respect to Ω. As a result, this provides new examples of weakly symmetric spaces that are nonsymmetric, including those already discovered by Selberg (cf. [M]) for the symplectic case and Berndt and Vanhecke [BV1] for the rank-one case.
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    Circuits, systems and signal processing 13 (1994), S. 19-30 
    ISSN: 1531-5878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology
    Notes: Abstract A linear-quadratic (LQ) control problem subject to a standard continuous-time system is called regular if the input weighting matrix is invertible, and singular if this is not the case. Consequently, optimal inputs for regular LQ problems are ordinary functions (state feedbacks), whereas optical controls for singular problems are in general distributions, e.g., impulses. We will show that regularity and singularity in LQ problems subject to ageneral (implicit) system depends not so much on the input weighting matrix, as on the property that the integrand of the cost criterion is a function only if inputs and state trajectories are, as is the case for LQ problems, subject to astandard system. In particular, we will provide a simple criterion for distinguishing between regularity and singularity in LQ problems subject to a general system. Our criterion is expressed in the system coefficients only and reduces to the classical one if the underlying system is standard.
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    Circuits, systems and signal processing 13 (1994), S. 119-119 
    ISSN: 1531-5878
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    Topics: Electrical Engineering, Measurement and Control Technology
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    Circuits, systems and signal processing 13 (1994), S. 185-199 
    ISSN: 1531-5878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology
    Notes: Abstract Completions of linear time varying singular systems of the formE(t)x′(t)+F(t)x′(t)=f(t) are explicitly computed using recent results on rational matrix functions. The algorithm and the theory behind it are carefully described. Computational issues are discussed.
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  • 97
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    Circuits, systems and signal processing 13 (1994), S. 225-239 
    ISSN: 1531-5878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology
    Notes: Abstract In this paper a spectral method using orthogonal periodic basis functions for the analysis of linear time invariant descriptor systems is discussed, and the case of the trigonometric Fourier functions is investigated in detail. The method is shown to be convergent, in the distributional sense. However, for any finite number of basis functions, the periodicity induced by the chosen basis can give rise to spurious impulsive components in the computed system response, even in the case of correct initial conditions.
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    Circuits, systems and signal processing 13 (1994), S. 295-308 
    ISSN: 1531-5878
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    Topics: Electrical Engineering, Measurement and Control Technology
    Notes: Abstract In this paper we will study topological properties of the class of proper and improperp×m transfer functions of a fixed McMillan degreen. A natural generalization of this class is all autoregressive systems of degreen under external system equivalence. The subset of irreducible systems has in a natural way the structure of a manifold and we show how to extend this topology to the set of all autoregressive systems of degree at mostn. We will describe the subset of systems with fixed Kronecker indicesv=(v1,...,v p ) as an orbit space, which will enable us to calculate the topological dimension for each collection of indicesv. Finally, we will describe the topological closure of those sets in the space of all autoregressive systems.
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    Circuits, systems and signal processing 13 (1994), S. 349-359 
    ISSN: 1531-5878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology
    Notes: Abstract It has been shown in [B.M.90] that non-square implicit differential equations allow for the description of variable structure systems (variable order, variable sign, variable parameters). We combine here the possible control strategy developed in [L.91] for rectangular systems (insuring a unique output behavior for the system compensated with a proportional or proportional and derivative state feedback) with the detector and the observer introduced in [B.M.90] in order to obtain a closed-loop system where the initial structure variation disappears on the output. We also give necessary and sufficient conditions for the free assignment of the associated output dynamics.
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    Circuits, systems and signal processing 13 (1994), S. 391-402 
    ISSN: 1531-5878
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology
    Notes: Abstract An exposition of joint cumulants and cumulant spectra is presented. A distinction is emphasized in this paper between the cumulant spectrum of a time series and its stationary version, here called apolyspectrum. The variance and covariance of the sample bispectrum is then derived using a relationship between cumulant spectra of the finite Fourier transform for the 2nd and 4th cumulant function, and the bispectrum and trispectrum of the time series.
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