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  1. Linear discrete models with different time scales.Eva Sánchez, Rafael Bravo de la Parra & Pierre Auger - 1995 - Acta Biotheoretica 43 (4):465-476.
    Aggregation of variables allows to approximate a large scale dynamical system involving many variables into a reduced system described by a few number of global variables. Approximate aggregation can be performed when different time scales are involved in the dynamics of the micro-system. Perturbation methods enable to approximate the large micro-system by a macro-system going on at a slow time scale. Aggregation has been performed for systems of ordinary differential equations in which time is a continuous variable. In this contribution, (...)
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  • Variables aggregation in time varying discrete systems.Luis Sanz & Rafael Bravo de la Parra - 1998 - Acta Biotheoretica 46 (3):273-297.
    In this work we extend approximate aggregation methods in time discrete linear models to the case of time varying environments. Approximate aggregation consists in describing some features of the dynamics of a general system involving many coupled variables in terms of the dynamics of a reduced system with a few number of variables. We present a time discrete time varying model in which we distinguish two time scales. By using perturbation methods we transform the system to make the global variables (...)
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  • The reliability of approximate reduction techniques in population models with two time scales.Luis Sanz & Rafael Bravo de la Parra - 2002 - Acta Biotheoretica 50 (4):297-322.
    As a result of the complexity inherent in some natural systems, mathematical models employed in ecology are often governed by a large number of variables. For instance, in the study of population dynamics we often find multiregional models for structured populations in which individuals are classified regarding their age and their spatial location. Dealing with such structured populations leads to high dimensional models. Moreover, in many instances the dynamics of the system is controlled by processes whose time scales are very (...)
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  • Influence of individual aggressiveness on the dynamics of competitive populations.Eva Sanchez, Pierre Auger & Rafael Bravo de la Parra - 1997 - Acta Biotheoretica 45 (3-4):321-333.
    Two populations are subdivided into two categories of individuals (hawks and doves). Individuals fight to have access to a resource which is necessary for their survival. Conflicts occur between individuals belonging to the same population and to different populations. We investigate the long term effects of the conflicts on the stability of the community. The modelis a set of ODE's with four variables corresponding to hawk and dove individuals of the two populations. Two time scales are considered. A fast time (...)
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  • Perturbations of the classical lotka-volterra system by behavioral sequences.Jean-Christophe Poggiale, Pierre Auger & Robert Roussarie - 1995 - Acta Biotheoretica 43 (1-2):27-39.
    The complexity and the variability of parameters occurring in ecological dynamical systems imply a large number of equations.Different methods, more or less successful, have been described to reduce this number of equations. For instance, in the paper of Auger and Roussarie (1993), the authors describe how to obtain a reduction by considering different time-scales. They consider a system which can be sub-divided into sub-systems such that the strengths of the intra-sub-systems interactions are much larger than those of the inter-sub-systems interactions. (...)
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  • Effect of Hawk-Dove Game on the Dynamics of Two Competing Species.Ali Moussaoui, Pierre Auger & Benjamin Roche - 2014 - Acta Biotheoretica 62 (3):385-404.
    Outcomes of interspecific competition, and especially the possibility of coexistence, have been extensively studied in theoretical ecology because of their implications in community assemblages. During the last decades, the influence of different time scales through the local/regional dynamics of animal communities has received an increasing attention. Nevertheless, different time scales involved in interspecific competition can result form other processes than spatial dynamics. Here, we envision and analyze a new theoretical framework that couples a game theory approach for competition with a (...)
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  • The dynamics of a fish stock exploited in two fishing zones.R. Mchich, P. Auger & N. Raïssi - 2000 - Acta Biotheoretica 48 (3-4):207-218.
    This work presents a specific stock-effort dynamical model. The stocks correspond to two populations of fish moving and growing between two fishery zones. They are harvested by two different fleets. The effort represents the number of fishing boats of the two fleets that operate in the two fishing zones. The bioeconomical model is a set of four ODE's governing the fishing efforts and the stocks in the two fishing areas. Furthermore, the migration of the fish between the two patches is (...)
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  • Effects of density dependent migrations on the dynamics of a predator prey model.Rachid Mchich, Amal Bergam & Nadia Raïssi - 2005 - Acta Biotheoretica 53 (4):331-340.
    We study the effects of density dependent migrations on the stability of a predator-prey model in a patchy environment which is composed with two sites connected by migration. The two patches are different. On the first patch, preys can find resource but can be captured by predators. The second patch is a refuge for the prey and thus predators do not have access to this patch. We assume a repulsive effect of predator on prey on the resource patch. Therefore, when (...)
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  • Reduction of Nonautonomous Population Dynamics Models with Two Time Scales.Marcos Marvá & Rafael Bravo de la Parra - 2014 - Acta Biotheoretica 62 (3):285-303.
    The purpose of this work is reviewing some reduction results to deal with systems of nonautonomous ordinary differential equations with two time scales. They could be included among the so-called approximate aggregation methods. The existence of different time scales in a system, together with some long-term features, are used to build up a simpler system governed by a lesser number of state variables. The asymptotic behavior of the latter system is then used to describe the asymptotic behaviour of the former (...)
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  • Population dynamics modelling in an hierarchical arborescent river network: An attempt with salmo trutta.S. Charles, R. Bravo de la Parra, J. P. Mallet, H. Persat & P. Auger - 1998 - Acta Biotheoretica 46 (3):223-234.
    The balance between births and deaths in an age-structured population is strongly influenced by the spatial distribution of sub-populations. Our aim was to describe the demographic process of a fish population in an hierarchical dendritic river network, by taking into account the possible movements of individuals. We tried also to quantify the effect of river network changes (damming or channelling) on the global fish population dynamics. The Salmo trutta life pattern was taken as an example for.We proposed a model which (...)
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  • On the Optimal Size of Marine Reserves.M. Bensenane, A. Moussaoui & P. Auger - 2013 - Acta Biotheoretica 61 (1):109-118.
    The excessive and unsustainable exploitation of our marine resources has led to the promotion of marine reserves as a fisheries management tool. Marine reserves, areas in which fishing is restricted or prohibited, can offer opportunities for the recovery of exploited stock and fishery enhancement. This study examines the impact of the creation of marine protected areas, from both economic and biological perspectives. The consequences of reserve establishment on the long-run equilibrium fish biomass and fishery catch levels are evaluated. We include (...)
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  • Aggregation and emergence in hierarchically organized systems: Population dynamics.Pierre Auger & Jean-Christophe Poggiale - 1996 - Acta Biotheoretica 44 (3-4):301-316.
    The aim of this work is to present aggregation methods of hierarchically organized systems allowing one to replace the initial micro-system by a macro-system described by a few global variables. We also study the relations between the fast micro-dynamics and the slow macro-dynamics which can produce global properties. Emergence corresponds to a bottom-up coupling that is the result effected by a micro-level at a macro-level. As an example, we present prey-predator models with different time scales in an heterogeneous environment. A (...)
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  • Corals and starfish devastation of the great barrier Reef: Aggregation methods.Peter Antonelli & Pierre Auger - 1995 - Acta Biotheoretica 43 (4):481-493.
    Aggregation methods allow one to replace a large scale dynamical system (micro-system) by a reduced dynamical system (macro-system) governing a small number of global variables. This aggregation of variables can be performed when two time scales exist, a fast time scale and a slow time scale. Perturbation theory allows to obtain an approximated aggregated dynamical system which describes the behaviour of a few number of slow time varying variables which are constants of motion of the fast part of the micro-system. (...)
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  • The fundamentals of vegetation change - complexity rules.M. Anand - 2000 - Acta Biotheoretica 48 (1):1-14.
    Long-term vegetation dynamics based on paleo-pollen data display transient behaviour, often alternating in phase between predominant determinism and predominant 'turbulence', when viewed as a trajectory in a multivariate phase space. Given this, the metaphor of vegetation dynamics as a 'flowing stream', first introduced by Cooper in his classic 1926 paper entitled "The fundamentals of vegetation change", is re-examined and revealed to be not only useful, but strikingly realistic. Vegetation dynamic theory is reviewed and classic theories are found to reflect reality (...)
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