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Claude Lobry

Publications and source records attributed to Claude Lobry.

14 recordsLinked to original sources

A flatness proof of the exponential turnpike phenomenon for linear-quadratic optimal control problems

We revisit finite-dimensional linear-quadratic optimal control from the viewpoint of differential flatness. If the pair (A, B) is controllable, then the linear control system is flat, and every trajectory can be parametrized by a flat output and finitely many of its derivatives. Once this parametrization is inserted into the quadratic functional, the Euler-Lagrange condition becomes a linear differential equation with constant coefficients, or more generally a polynomial matrix differential equation. After reduction to Smith normal form, this equation decouples into scalar constant-coefficient equations, and its solutions are exponentialpolynomials. This yields a viewpoint on the turnpike phenomenon that is quite different from the classical Hamiltonian-Riccati analysis: the turnpike mechanism appears directly from the stable-unstable splitting of the reduced flat equation. In particular, when the reduced Euler-Lagrange operator has no purely imaginary characteristic roots and when the endpoint constraints act nondegenerately on the stable and unstable modes, the optimal trajectory consists of a left-boundary layer, a right-boundary layer, and a long interior arc exponentially close to the static optimum. The same viewpoint also clarifies what changes when some weights are only semidefinite: the order of the reduced equation may drop, some endpoint conditions may become incompatible, and polynomial or oscillatory modes may destroy the exponential turnpike. It also gives a natural meaning to certain endpoint constraints on the control and on finitely many derivatives of the control: such traces are not defined on the ambient L 2 control space, but they are meaningful on the smooth extremals selected by the reduced Euler-Lagrange equation. We formulate this principle as a general theorem and illustrate it in detail on the double integrator.

math.OC

Evolution du Principe d'Exclusion Comp\'etitive : Le r\^ole des math\'ematiques

Everyone can see that over the last 150 years, theoretical ecology has become considerably more mathematical. But what is the nature of this phenomenon? Are mathematics applied, as in the use of statistical tests, for example, or are they involved, as in physics, where laws cannot be expressed without them? Through the history of the {\em Competitive Exclusion Principle} formulated at the very beginning of the 20th century by the naturalist Grinnell concerning the distribution of brown-backed chickadees, up to its modern integration into what is known in mathematics as population dynamics, I highlight the effectiveness of what could be called the mathematical novel in clarifying certain concepts in theoretical ecology.

q-bio.PE

Sufficient condition for dispersal-induced growth on dynamic networks

We consider a population spreading across a finite number of sites. Individuals can move from one site to the other according to a network (oriented links between the sites) that vary periodically over time. On each site, the population experiences a growth rate which is also periodically time varying. Recently, this kind of models have been extensively studied, using various technical tools to derive precise necessary and sufficient conditions on the parameters of the system (ie the local growth rate on each site, the time period and the strength of migration between the sites) for the population to grow. In the present paper, we take a completely different approach: using elementary comparison results between linear systems, we give sufficient condition for the growth of the population This condition is easy to check and can be applied in a broad class of examples. In particular, in the case when all sites are sinks (ie, in the absence of migration, the population become extinct in each site), we prove that when our condition of growth if satisfied, the population grows when the time period is large and for values of the migration strength that are exponentially small with respect to the time period, which answers positively to a conjecture stated by Katriel.

math.DS

Dispersal-induced growth or decay in a time-periodic environment. The case of reducible migration matrices

This paper is a follow-up to a previous work where we considered populations with time-varying growth rates living in patches and irreducible migration matrix between the patches. Each population, when isolated, would become extinct. Dispersal-induced growth (DIG) occurs when the populations are able to persist and grow exponentially when dispersal among the populations is present. In this paper, we consider the situation where the migration matrix is not necessarily irreducible. We provide a mathematical analysis of the DIG phenomenon, in the context of a deterministic model with periodic variation of growth rates and migration. Our results apply in the case, important for applications, where there is migration in one direction in one season and in the other direction in another season. We also consider dispersal-induced decay (DID), where each population, when isolated, grows exponentially, while populations die out when dispersal between populations is present.

math.DS

When can a population spreading across sink habitats persist ?

We consider populations with time-varying growth rates living in sinks. Each population, when isolated, would become extinct. Dispersal-induced growth (DIG) occurs when the populations are able to persist and grow exponentially when dispersal among the populations is present. We provide a mathematical analysis of this surprising phenomenon, in the context of a deterministic model with periodic variation of growth rates and non-symmetric migration which are assumed to be piecewise continuous. We also consider a stochastic model with random variation of growth rates and migration. This work extends existing results of the literature on the DIG effects obtained for periodic continuous growth rates and time independent symmetric migration.

math.DS

A note on the top Lyapunov exponent of linear cooperative systems

In a recent paper [Asymptotic of the largest Floquet multiplier for cooperative matrices Annales de la Facult\'e des Sciences de Toulouse, Tome XXXI, no 4 (2022)] P. Carmona gives an asymptotic formulae for the top Lyapunov exponent of a linear T-periodic cooperative differential equation, in the limit T goes to infinity. This short note discusses and extends this result.

math.DS

Entry-exit in the halo of a slow semi-stable curve

We consider a slow-fast differential system (SF) in dimension two which appears in the study of some linear model (LM) with periodic coefficients in population dynamics. We show existence of "canard solutions" of (SF) along semi-stable slow curve which explains some stability properties of (LM) when the period tends to infinity.

math.DS

Entr\'ee-sortie dans le halo d'une courbe lente semi-stable

We consider a slow-fast differential system (SF) in dimension two which appears in the study of some linear model (LM) with periodic coefficients in population dynamics. We show existence of "canard solutions" of (SF) along semi-stable slow curve which explains some stability properties of (LM) when the period tends to infinity.

math.DS

Untangling the role of temporal and spatial variations in persistance of populations

We consider a population distributed between two habitats, in each of which it experiences a growth rate that switches periodically between two values, $1- \varepsilon > 0$ or $ - (1 + \varepsilon) < 0$. We study the specific case where the growth rate is positive in one habitat and negative in the other one for the first half of the period, and conversely for the second half of the period, that we refer as the $(\pm 1)$ model. In the absence of migration, the population goes to $0$ exponentially fast in each environment. In this paper, we show that, when the period is sufficiently large, a small dispersal between the two patches is able to produce a very high positive exponential growth rate for the whole population, a phenomena called inflation. We prove in particular that the threshold of the dispersal rate at which the inflation appears is exponentially small with the period. We show that inflation is robust to random perturbation, by considering a model where the values of the growth rate in each patch are switched at random times: we prove, using theory of Piecewise Deterministic Markov Processes (PDMP) that inflation occurs for low switching rate and small dispersal. Finally, we provide some extensions to more complicated models, especially epidemiological and density dependent models.

math.DS

Approaches to analysis with infinitesimals following Robinson, Nelson, and others

This is a survey of several approaches to the framework for working with infinitesimals and infinite numbers, originally developed by Abraham Robinson in the 1960s, and their constructive engagement with the Cantor-Dedekind postulate and the Intended Interpretation hypothesis. We highlight some applications including (1) Loeb's approach to the Lebesgue measure, (2) a radically elementary approach to the vibrating string, (3) true infinitesimal differential geometry. We explore the relation of Robinson's and related frameworks to the multiverse view as developed by Hamkins. Keywords: axiomatisations, infinitesimal, nonstandard analysis, ultraproducts, superstructure, set-theoretic foundations, multiverse, naive integers, intuitionism, soritical properties, ideal elements, protozoa.

math.CA

Extensions of the chemostat model with flocculation

In this work, we study a model of the chemostat where the species are present in two forms, isolated bacteria and under an aggregated form like attached bacteria or bacteria in flocks. We show that our general model contains a lot of models which were previously considered in the literature. Assuming that flocculation and deflocculation dynamics are fast with respect to the growth of the species, we construct a reduced chemostat-like model in which both the growth functions and the apparent dilution rate depend on the density of the species. We also show that such a model involving monotonic growth rates may exhibit bistability, while it may only occur in the classical chemostat model when the growth rate in non monotonic.

math.DS

Effect of population size in a Prey-Predator model

We consider a stochastic version of the basic predator-prey differential equation model. The model, which contains a parameter ωwhich represents the number of individuals for one unit of prey -- If x denotes the quantity of prey in the differential equation model x = 1 means that there are ωindividuals in the discontinuous one -- is derived from the classical birth and death process. It is shown by the mean of simulations and explained by a mathematical analysis based on results in singular perturbation theory (the so called theory of Canards) that qualitative properties of the model like persistence or extinction are dramatically sensitive to ω. For instance, in our example, if ω= 107 we have extinction and if ω= 108 we have persistence. This means that we must be very cautious when we use continuous variables in place of jump processes in dynamic population modeling even when we use stochastic differential equations in place of deterministic ones.

math.DS

An effective model for flocculating bacteria with density-dependent growth dynamics

We present a model for a biological reactor in which bacteria tend to aggregate in flocs, as encountered in wastewater treatment plants. The influence of this flocculation on the growth dynamics of the bacteria is studied. We argue that a description in terms of a specific growth rate is possible when the flocculation dynamics is much faster than the other processes in the system. An analytical computation shows that in this case, the growth rate is density-dependent, i.e., depends both on the substrate and the biomass density. When the flocculation time scale overlaps with the other time scales present in the system, the notion of specific growth rate becomes problematic. However, we show numerically that a density-dependent growth rate can still accurately describe the system response to certain perturbations.

q-bio.PE