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Register a new userCompetitive Exclusion in a DAE Model for Microbial Electrolysis Cells
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Microbial electrolysis cells (MECs) employ electroactive bacteria to perform extracellular electron transfer, enabling hydrogen generation from biodegradable substrates. In previous work, we developed and analyzed a differential-algebraic equation (DAE) model for MECs. The model resembles a chemostat with ordinary differential equations (ODEs) for concentrations of substrate, microorganisms, and an extracellular mediator involved in electron transfer. There is also an algebraic constraint for electric current and hydrogen production. Our goal is to determine the outcome of competition between methanogenic archaea and electroactive bacteria, because only the latter contribute to electric current and resulting hydrogen production. We investigate asymptotic stability in two industrially releva
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Microbial electrolysis cells (MECs) are a promising new technology for producing hydrogen cheaply, efficiently, and sustainably. However, to scale up this technology, we need a better understanding of the processes in the devices. In this effort, we present a differential-algebraic equation (DAE) model of a microbial electrolysis cell with an algebraic constraint on current. We then perform sensitivity and bifurcation analysis for the DAE system. The model can be applied either to batch-cycle MECs or to continuous-flow MECs. We conduct differential-algebraic sensitivity analysis after fitting simulations to current density data for a batch-cycle MEC. The sensitivity analysis suggests which parameters have the greatest influence on the current density at particular times during the experiment. In particular, growth and consumption parameters for exoelectrogenic bacteria have a strong effect prior to the peak current density. An alternative strategy to maximizing peak current density is maintaining a long term stable equilibrium with non-zero current density in a continuous-flow MEC. We characterize the minimum dilution rate required for a stable nonzero current equilibrium and demonstrate transcritical bifurcations in the dilution rate parameter that exchange stability between several curves of equilibria. Specifically, increasing the dilution rate transitions the system through three regimes where the stable equilibrium exhibits (i) competitive exclusion by methanogens, (ii) coexistence, and (iii) competitive exclusion by exolectrogens. Positive long term current production is only feasible in the final two regimes. These results suggest how to modify system parameters to increase peak current density in a batch-cycle MEC or to increase the long term current density equilibrium value in a continuous-flow MEC.
Explaining biodiversity in nature is a fundamental problem in ecology. An outstanding challenge is embodied in the so-called Competitive Exclusion Principle: two species competing for one limiting resource cannot coexist at constant population densities, or more generally, the number of consumer species in steady coexistence cannot exceed that of resources. The fact that competitive exclusion is rarely observed in natural ecosystems has not been fully understood. Here we show that by forming chasing triplets among the consumers and resources in the consumption process, the Competitive Exclusion Principle can be naturally violated. The modeling framework developed here is broadly applicable and can be used to explain the biodiversity of many consumer-resource ecosystems and hence deepens our understanding of biodiversity in nature.
Microorganisms live in environments that inevitably fluctuate between mild and harsh conditions. As harsh conditions may cause extinctions, the rate at which fluctuations occur can shape microbial communities and their diversity, but we still lack an intuition on how. Here, we build a mathematical model describing two microbial species living in an environment where substrate supplies randomly switch between abundant and scarce. We then vary the rate of switching as well as different properties of the interacting species, and measure the probability of the weaker species driving the stronger one extinct. We find that this probability increases with the strength of demographic noise under harsh conditions and peaks at either low, high, or intermediate switching rates depending on both species ability to withstand the harsh environment. This complex relationship shows why finding patterns between environmental fluctuations and diversity has historically been difficult. In parameter ranges where the fittest species was most likely to be excluded, however, the beta diversity in larger communities also peaked. In sum, how environmental fluctuations affect interactions between a few species pairs predicts their effect on the beta diversity of the whole community.
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.
Surveys of microbial biodiversity such as the Earth Microbiome Project (EMP) and the Human Microbiome Project (HMP) have revealed robust ecological patterns across different environments. A major goal in ecology is to leverage these patterns to identify the ecological processes shaping microbial ecosystems. One promising approach is to use minimal models that can relate mechanistic assumptions at the microbe scale to community-level patterns. Here, we demonstrate the utility of this approach by showing that the Microbial Consumer Resource Model (MiCRM) -- a minimal model for microbial communities with resource competition, metabolic crossfeeding and stochastic colonization -- can qualitatively reproduce patterns found in survey data including compositional gradients, dissimilarity/overlap correlations, richness/harshness correlations, and nestedness of community composition. By using the MiCRM to generate synthetic data with different environmental and taxonomical structure, we show that large scale patterns in the EMP can be reproduced by considering the energetic cost of surviving in harsh environments and HMP patterns may reflect the importance of environmental filtering in shaping competition. We also show that recently discovered dissimilarity-overlap correlations in the HMP likely arise from communities that share similar environments rather than reflecting universal dynamics. We identify ecologically meaningful changes in parameters that alter or destroy each one of these patterns, suggesting new mechanistic hypotheses for further investigation. These findings highlight the promise of minimal models for microbial ecology.
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