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Jose A. Capitan

Publications and source records attributed to Jose A. Capitan.

16 recordsLinked to original sources

Out-of-equlibrium inference of feeding rates through population data from generic consumer-resource stochastic dynamics

Statistical models are often structurally unidentifiable, because different sets of parameters can lead to equal model outcomes. To be useful for prediction and parameter inference from data, stochastic population models need to be identifiable, this meaning that model parameters can be uniquely inferred from a large number of model observations. In particular, precise estimation of feeding rates in consumer-resource dynamics is crucial, because consumer-resource processes are central in determining biomass transport across ecosystems. Model parameters are usually estimated at stationarity, because in that case model analyses are often easier. In this contribution we analyze the problem of parameter redundancy in a multi-resource consumer-resource model, showing that model indentifiability depends on whether the dynamics have reached stationarity or not. To be precise, we: (i) Calculate the steady-state and out-of-equilibrium probability distributions of predator's abundances analytically using generating functions, which allow us to unveil parameter redundancy and carry out proper maximum likelihood estimation. (ii) Conduct \emph{in silico} experiments by tracking the abundance of consumers that are either searching for or handling prey, data then used for maximum likelihood parameter estimation. (iii) Show that, when model observations are recorded out of equilibrium, feeding parameters are truly identifiable, whereas if sampling is done solely at stationarity, only ratios of rates can be inferred from data (i.e., parameters are redundant). We discuss the implications of our results when inferring parameters of general dynamical models.

q-bio.PE

Effects of phylogeny on coexistence in model communities

Species' interactions are shaped by their traits. Thus, we expect traits -- in particular, trait (dis)similarity -- to play a central role in determining whether a particular set of species coexists. Traits are, in turn, the outcome of an eco-evolutionary process summarized by a phylogenetic tree. Therefore, the phylogenetic tree associated with a set of species should carry information about the dynamics and assembly properties of the community. Many studies have highlighted the potentially complex ways in which this phylogenetic information is translated into species' ecological properties. However, much less emphasis has been placed on developing clear, quantitative expectations for community properties under a particular hypothesis. To address this gap, we couple a simple model of trait evolution on a phylogenetic tree with Lotka-Volterra community dynamics. This allows us to derive properties of a community of coexisting species as a function of the number of traits, tree topology and the size of the species pool. Our analysis highlights how phylogenies, through traits, affect the coexistence of a set of species. Together, these results provide much-needed baseline expectations for the ways in which evolutionary history, summarized by phylogeny, is reflected in the size and structure of ecological communities.

q-bio.PE

A signal of competitive dominance in mid-latitude herbaceous plant communities

Understanding the main determinants of species coexistence across space and time is a central question in ecology. However, ecologists still know little about the scales and conditions at which biotic interactions matter and how these interact with the environment to structure species assemblages. Here we use recent theory developments to analyze plant distribution and trait data across Europe and find that plant height clustering is related to both evapotranspiration and gross primary productivity. This clustering is a signal of interspecies competition between plants, which is most evident in mid-latitude ecoregions, where conditions for growth (reflected in actual evapotranspiration rates and gross primary productivities) are optimal. Away from this optimum, climate severity likely overrides the effect of competition, or other interactions become increasingly important. Our approach bridges the gap between species-rich competition theories and large-scale species distribution data analysis.

q-bio.PE

Competitive dominance in plant communities: Modeling approaches and theoretical predictions

Quantitative predictions about the processes that promote species coexistence are a subject of active research in ecology. In particular, competitive interactions are known to shape and maintain ecological communities, and situations where some species out-compete or dominate over some others are key to describe natural ecosystems. Here we develop ecological theory using a stochastic, synthetic framework for plant community assembly that leads to predictions amenable to empirical testing. We propose two stochastic continuous-time Markov models that incorporate competitive dominance through a hierarchy of species heights. The first model, which is spatially implicit, predicts both the expected number of species that survive and the conditions under which heights are clustered in realized model communities. The second one allows spatially-explicit interactions of individuals and alternative mechanisms that can help shorter plants overcome height-driven competition, and it demonstrates that clustering patterns remain not only locally but also across increasing spatial scales. Moreover, although plants are actually height-clustered in the spatially-explicit model, it allows for plant species abundances not necessarily skewed to taller plants.

q-bio.PE

Integrability of Stochastic Birth-Death processes via Differential Galois Theory

Stochastic birth-death processes are described as continuous-time Markov processes in models of population dynamics. A system of infinite, coupled ordinary differential equations (the so-called master equation) describes the time-dependence of the probability of each system state. Using a generating function, the master equation can be transformed into a partial differential equation. In this contribution we analyze the integrability of two types of stochastic birth-death processes (with polynomial birth and death rates) using standard differential Galois theory. We discuss the integrability of the PDE via a Laplace transform acting over the temporal variable. We show that the PDE is not integrable except for the (trivial) case in which rates are linear functions of the number of individuals.

math-ph

Stochastic competitive exclusion leads to a cascade of species extinctions

Community ecology has traditionally relied on the competitive exclusion principle, a piece of common wisdom in conceptual frameworks developed to describe species assemblages. Key concepts in community ecology, such as limiting similarity and niche partitioning, are based on competitive exclusion. However, this classical paradigm in ecology relies on implications derived from simple, deterministic models. Here we show how the predictions of a symmetric, deterministic model about the way extinctions proceed can be utterly different from the results derived from the same model when ecological drift (demographic stochasticity) is explicitly considered. Using analytical approximations to the steady-state conditional probabilities for assemblages with two and three species, we demonstrate that stochastic competitive exclusion leads to a cascade of extinctions, whereas the symmetric, deterministic model predicts a multiple collapse of species. To test the robustness of our results, we have studied the effect of environmental stochasticity and relaxed the species symmetry assumption. Our conclusions highlight the crucial role of stochasticity when deriving reliable theoretical predictions for species community assembly.

q-bio.PE

Demography-based adaptive network model reproduces the spatial organization of human linguistic groups

The distribution of human linguistic groups presents a number of interesting and non-trivial patterns. The distributions of the number of speakers per language and the area each group covers follow log-normal distributions, while population and area fulfill an allometric relationship. The topology of networks of spatial contacts between different linguistic groups has been recently characterized, showing atypical properties of the degree distribution and clustering, among others. Human demography, spatial conflicts, and the construction of networks of contacts between linguistic groups are mutually dependent processes. Here we introduce an adaptive network model that takes all of them into account and successfully reproduces, using only four model parameters, not only those features of linguistic groups already described in the literature, but also correlations between demographic and topological properties uncovered in this work. Besides their relevance when modeling and understanding processes related to human biogeography, our adaptive network model admits a number of generalizations that broaden its scope and make it suitable to represent interactions between agents based on population dynamics and competition for space.

q-bio.PE

The struggle for space: Viral extinction through competition for cells

The design of protocols to suppress the propagation of viral infections is an enduring enterprise, especially hindered by limited knowledge of the mechanisms through which extinction of infection propagation comes about. We here report on a mechanism causing extinction of a propagating infection due to intraspecific competition to infect susceptible hosts. Beneficial mutations allow the pathogen to increase the production of progeny, while the host cell is allowed to develop defenses against infection. When the number of susceptible cells is unlimited, a feedback runaway co-evolution between host resistance and progeny production occurs. However, physical space limits the advantage that the virus can obtain from increasing offspring numbers, thus infection clearance may result from an increase in host defenses beyond a finite threshold. Our results might be relevant to better understand propagation of viral infections in tissues with mobility constraints, and the implications that environments with different geometrical properties might have in devising control strategies.

q-bio.PE

Species assembly in model ecosystems, I: Analysis of the population model and the invasion dynamics

Recently we have introduced a simplified model of ecosystem assembly (Capitan et al., 2009) for which we are able to map out all assembly pathways generated by external invasions in an exact manner. In this paper we provide a deeper analysis of the model, obtaining analytical results and introducing some approximations which allow us to reconstruct the results of our previous work. In particular, we show that the population dynamics equations of a very general class of trophic-level structured food-web have an unique interior equilibrium point which is globally stable. We show analytically that communities found as end states of the assembly process are pyramidal and we find that the equilibrium abundance of any species at any trophic level is approximately inversely proportional to the number of species in that level. We also find that the per capita growth rate of a top predator invading a resident community is key to understand the appearance of complex end states reported in our previous work. The sign of these rates allows us to separate regions in the space of parameters where the end state is either a single community or a complex set containing more than one community. We have also built up analytical approximations to the time evolution of species abundances that allow us to determine, with high accuracy, the sequence of extinctions that an invasion may cause. Finally we apply this analysis to obtain the communities in the end states. To test the accuracy of the transition probability matrix generated by this analytical procedure for the end states, we have compared averages over those sets with those obtained from the graph derived by numerical integration of the Lotka-Volterra equations. The agreement is excellent.

q-bio.PE

Species assembly in model ecosystems, II: Results of the assembly process

In the companion paper of this set (Capitan and Cuesta, 2010) we have developed a full analytical treatment of the model of species assembly introduced in Capitan et al. (2009). This model is based on the construction of an assembly graph containing all viable configurations of the community, and the definition of a Markov chain whose transitions are the transformations of communities by new species invasions. In the present paper we provide an exhaustive numerical analysis of the model, describing the average time to the recurrent state, the statistics of avalanches, and the dependence of the results on the amount of available resource. Our results are based on the fact that the Markov chain provides an asymptotic probability distribution for the recurrent states, which can be used to obtain averages of observables as well as the time variation of these magnitudes during succession, in an exact manner. Since the absorption times into the recurrent set are found to be comparable to the size of the system, the end state is quickly reached (in units of the invasion time). Thus, the final ecosystem can be regarded as a fluctuating complex system where species are continually replaced by newcomers without ever leaving the set of recurrent patterns. The assembly graph is dominated by pathways in which most invasions are accepted, triggering small extinction avalanches. Through the assembly process, communities become less resilient (e.g., have a higher return time to equilibrium) but become more robust in terms of resistance against new invasions.

q-bio.PE

A scale-invariant model of marine population dynamics

A striking feature of the marine ecosystem is the regularity in its size spectrum: the abundance of organisms as a function of their weight approximately follows a power law over almost ten orders of magnitude. We interpret this as evidence that the population dynamics in the ocean is approximately scale-invariant. We use this invariance in the construction and solution of a size-structured dynamical population model. Starting from a Markov model encoding the basic processes of predation, reproduction, maintenance respiration and intrinsic mortality, we derive a partial integro-differential equation describing the dependence of abundance on weight and time. Our model represents an extension of the jump-growth model and hence also of earlier models based on the McKendrick--von Foerster equation. The model is scale-invariant provided the rate functions of the stochastic processes have certain scaling properties. We determine the steady-state power law solution, whose exponent is determined by the relative scaling between the rates of the density-dependent processes (predation) and the rates of the density-independent processes (reproduction, maintenance, mortality). We study the stability of the steady-state against small perturbations and find that inclusion of maintenance respiration and reproduction in the model has astrong stabilising effect. Furthermore, the steady state is unstable against a change in the overall population density unless the reproduction rate exceeds a certain threshold.

q-bio.PE

Catastrophic regime shifts in model ecological communities are true phase transitions

Ecosystems often undergo abrupt regime shifts in response to gradual external changes. These shifts are theoretically understood as a regime switch between alternative stable states of the ecosystem dynamical response to smooth changes in external conditions. Usual models introduce nonlinearities in the macroscopic dynamics of the ecosystem that lead to different stable attractors among which the shift takes place. Here we propose an alternative explanation of catastrophic regime shifts based on a recent model that pictures ecological communities as systems in continuous fluctuation, according to certain transition probabilities, between different micro-states in the phase space of viable communities. We introduce a spontaneous extinction rate that accounts for gradual changes in external conditions, and upon variations on this control parameter the system undergoes a regime shift with similar features to those previously reported. Under our microscopic viewpoint we recover the main results obtained in previous theoretical and empirical work (anomalous variance, hysteresis cycles, trophic cascades). The model predicts a gradual loss of species in trophic levels from bottom to top near the transition. But more importantly, the spectral analysis of the transition probability matrix allows us to rigorously establish that we are observing the fingerprints, in a finite size system, of a true phase transition driven by background extinctions.

q-bio.PE

Phase diagram of a two-dimensional lattice gas model of a ramp system

Using Monte Carlo Simulation and fundamental measure theory we study the phase diagram of a two-dimensional lattice gas model with a nearest neighbor hard core exclusion and a next-to-nearest neighbors finite repulsive interaction. The model presents two competing ranges of interaction and, in common with many experimental systems, exhibits a low density solid phase, which melts back to the fluid phase upon compression. The theoretical approach is found to provide a qualitatively correct picture of the phase diagram of our model system.

cond-mat.soft

Phase behavior of parallel hard cylinders

We test the performance of a recently proposed fundamental measure density functional of aligned hard cylinders by calculating the phase diagram of a monodisperse fluid of these particles. We consider all possible liquid crystalline symmetries, namely nematic, smectic and columnar, as well as the crystalline phase. For this purpose we introduce a Gaussian parameterization of the density profile and use it to minimize numerically the functional. We also determine, from the analytic expression for the structure factor of the uniform fluid, the bifurcation points from the nematic to the smectic and columnar phases. The equation of state, as obtained from functional minimization, is compared to the available Monte Carlo simulation. The agreement is is very good, nearly perfect in the description of the inhomogeneous phases. The columnar phase is found to be metastable with respect to the smectic or crystal phases, its free energy though being very close to that of the stable phases. This result justifies the observation of a window of stability of the columnar phase in some simulations, which disappears as the size of the system increases. The only important deviation between theory and simulations shows up in the location of the nematic-smectic transition. This is the common drawback of any fundamental measure functional of describing the uniform phase just with the accuracy of scaled particle theory.

cond-mat.soft

A fundamental-measure density functional for mixtures of parallel hard cylinders

We obtain a fundamental measure density functional for mixtures of parallel hard cylinders. To this purpose we first generalize to multicomponent mixtures the fundamental measure functional proposed by Tarazona and Rosenfeld for a one-component hard disk fluid, through a method alternative to the cavity formalism of these authors. We show the equivalence of both methods when applied to two-dimensional fluids. The density functional so obtained reduces to the exact density functional for one-dimensional mixtures of hard rods when applied to one-dimensional profiles. In a second step we apply an idea put forward some time ago by two of us, based again on a dimensional reduction of the system, and derive a density functional for mixtures of parallel hard cylinders. We explore some features of this functional by determining the fluid-fluid demixing spinodals for a binary mixture of cylinders with the same volume, and by calculating the direct correlation functions.

cond-mat.soft

Fundamental-measure density functional for the fluid of aligned hard hexagons: New insights in fundamental measure theory

In this article we obtain a fundamental measure functional for the model of aligned hard hexagons in the plane. Our aim is not just to provide a functional for a new, admittedly academic, model, but to investigate the structure of fundamental measure theory. A model of aligned hard hexagons has similarities with the hard disk model. Both share "lost cases", i.e. admit configurations of three particles in which there is pairwise overlap but not triple overlap. These configurations are known to be problematic for fundamental measure functionals, which are not able to capture their contribution correctly. This failure lies in the inability of these functionals to yield a correct low density limit of the third order direct correlation function. Here we derive the functional by projecting aligned hard cubes on the plane x+y+z=0. The correct dimensional crossover behavior of these functionals permits us to follow this strategy. The functional of aligned hard cubes, however, does not have lost cases, so neither had the resulting functional for aligned hard hexagons. The latter exhibits, in fact, a peculiar structure as compared to the one for hard disks. It depends on a uniparametric family of weighted densities through a new term not appearing in the functional for hard disks. Apart from studying the freezing of this system, we discuss the implications of the functional structure for new developments of fundamental measure theory.

cond-mat.soft