stochastic logistic model
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2021 ◽  
Author(s):  
Silvia Zaoli ◽  
Jacopo Grilli

The large taxonomic variability of microbial community composition is a consequence of the combination of environmental variability, mediated through ecological interactions, and stochasticity. Most of the analysis aiming to infer the biological factors determining this difference in community structure start by quantifying how much communities are similar in their composition, trough beta-diversity metrics. The central role that these metrics play in microbial ecology does not parallel with a quantitative understanding of their relationships and statistical properties. In particular, we lack a framework that reproduces the empirical statistical properties of beta-diversity metrics. Here we take a macroecological approach and introduce a model to reproduce the statistical properties of community similarity. The model is based on the statistical properties of individual communities and on a single tunable parameter, the correlation of species' carrying capacities across communities, which sets the difference of two communities. The model reproduces quantitatively the empirical values of several commonly-used beta-diversity metrics, as well as the relationships between them. In particular, this modeling framework naturally reproduces the negative correlation between overlap and dissimilarity, which has been observed in both empirical and experimental communities and previously related to the existence of universal features of community dynamics. In this framework, such correlation naturally emerges due to the effect of random sampling.


2021 ◽  
Vol 83 (10) ◽  
Author(s):  
A. C. Fowler

AbstractThis paper addresses the problem of extinction in continuous models of population dynamics associated with small numbers of individuals. We begin with an extended discussion of extinction in the particular case of a stochastic logistic model, and how it relates to the corresponding continuous model. Two examples of ‘small number dynamics’ are then considered. The first is what Mollison calls the ‘atto-fox’ problem (in a model of fox rabies), referring to the problematic theoretical occurrence of a predicted rabid fox density of $$10^{-18}$$ 10 - 18 (atto-) per square kilometre. The second is how the production of large numbers of eggs by an individual can reliably lead to the eventual survival of a handful of adults, as it would seem that extinction then becomes a likely possibility. We describe the occurrence of the atto-fox problem in other contexts, such as the microbial ‘yocto-cell’ problem, and we suggest that the modelling resolution is to allow for the existence of a reservoir for the extinctively challenged individuals. This is functionally similar to the concept of a ‘refuge’ in predator–prey systems and represents a state for the individuals in which they are immune from destruction. For what I call the ‘frogspawn’ problem, where only a few individuals survive to adulthood from a large number of eggs, we provide a simple explanation based on a Holling type 3 response and elaborate it by means of a suitable nonlinear age-structured model.


2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Jacopo Grilli

Abstract How the coexistence of many species is maintained is a fundamental and unresolved question in ecology. Coexistence is a puzzle because we lack a mechanistic understanding of the variation in species presence and abundance. Whether variation in ecological communities is driven by deterministic or random processes is one of the most controversial issues in ecology. Here, I study the variation of species presence and abundance in microbial communities from a macroecological standpoint. I identify three macroecological laws that quantitatively characterize the fluctuation of species abundance across communities and over time. Using these three laws, one can predict species’ presence and absence, diversity, and commonly studied macroecological patterns. I show that a mathematical model based on environmental stochasticity, the stochastic logistic model, quantitatively predicts the three macroecological laws, as well as non-stationary properties of community dynamics.


Complexity ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-24
Author(s):  
Haokun Qi ◽  
Hua Guo

In this paper, we propose and discuss a stochastic logistic model with delay, Markovian switching, Lévy jump, and two-pulse perturbations. First, sufficient criteria for extinction, nonpersistence in the mean, weak persistence, persistence in the mean, and stochastic permanence of the solution are gained. Then, we investigate the lower (upper) growth rate of the solutions. At last, we make use of Matlab to illustrate the main results and give an explanation of biological implications: the large stochastic disturbances are disadvantageous for the persistence of the population; excessive impulsive harvesting or toxin input can lead to extinction of the population.


Author(s):  
Daniel Ochieng Achola

Objectives: To develop a mathematical model that incorporates genetic defect in estimating the growth rate of roan antelopes in Ruma National Park,Kenya.Methodology: This study has developed an improved Oksendal and Lungu’s stochastic logistic model to estimates population growth rate of roans by incorporating genetic defect that were not considered by Magin and Cock. Appropriate adjustments were made to Vortex version 9.99 a computer simulation programme to simulate the extinction process.Results: There is a high-level impact between inbreeding and population growth(survival) in small populations. Supplementation of both juvenile and adult roans ensured population survival for longer period.Conclusion: Due to unpredictable consequences to the ecosystem and conflict with wildlife management policies in protected areas, this paper recommends supplementation instead of predator control to curb inbreeding which is a major threat to small populations. Supplementation should be done in phases without causing disruption to social groups.


2020 ◽  
Vol 12 (2) ◽  
pp. 52
Author(s):  
Tawfiqullah Ayoubi ◽  
Abdul Munir Khirzada

In this research, we first prove that the stochastic logistic model (10) has a positive global solution. Subsequently, we introduce the sufficient conditions for the stochastically stability of the general form of stochastic differential equations (SDEs) in terms of equation (1), for zero solution by using the Lyapunov function. This result is verified via several examples in Appendix A. Besides; we prove that the stochastic logistic model, by incorporating the Ornstein-Uhlenbeck process is stable in zero solution. Furthermore, the simulated results are displayed via the 4-stage stochastic Runge-Kutta (SRK4) numerical method.


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