ratio dependent
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2022 ◽  
Vol 40 ◽  
pp. 1-20
Author(s):  
Parisa Azizi ◽  
Reza Khoshsiar Ghaziani

In this paper, we study a ratio-dependent predator-prey model with modied Holling-Tanner formalism, by using dynamical techniques and numerical continuation algorithms implemented in Matcont. We determine codim-1 and 2 bifurcation points and their corresponding normal form coecients. We also compute a curve of limit cycles of the system emanating from a Hopf point.


2021 ◽  
Vol 9 ◽  
Author(s):  
Yuri V. Tyutyunov ◽  
Lyudmila I. Titova

The functional response (trophic function or individual ration) quantifies the average amount of prey consumed per unit of time by a single predator. Since the seminal Lotka-Volterra model, it is a key element of the predation theory. Holling has enhanced the theory by classifying prey-dependent functional responses into three types that long remained a generally accepted basis of modeling predator-prey interactions. However, contradictions between the observed dynamics of natural ecosystems and the properties of predator-prey models with Holling-type trophic functions, such as the paradox of enrichment, the paradox of biological control, and the paradoxical enrichment response mediated by trophic cascades, required further improvement of the theory. This led to the idea of the inclusion of predator interference into the trophic function. Various functional responses depending on both prey and predator densities have been suggested and compared in their performance to fit observed data. At the end of the 1980s, Arditi and Ginzburg stimulated a lively debate having a strong impact on predation theory. They proposed the concept of a spectrum of predator-dependent trophic functions, with two opposite edges being the prey-dependent and the ratio-dependent cases, and they suggested revising the theory by using the ratio-dependent edge of the spectrum as a null model of predator interference. Ratio-dependence offers the simplest way of accounting for mutual interference in predator-prey models, resolving the abovementioned contradictions between theory and natural observations. Depending on the practical needs and the availability of observations, the more detailed models can be built on this theoretical basis.


Mathematics ◽  
2021 ◽  
Vol 9 (21) ◽  
pp. 2776
Author(s):  
Wen Liu ◽  
Jianfeng Feng

In this paper, we focus on the asymptotic and transient dynamics of the studied ecosystem and measure the response to perturbation of the stochastic ratio-dependent predator–prey model. The method we use is mainly based on the Kronecker product and numerical simulation. Firstly, the mean-square stability matrix can be calculated from the Kronecker product, so as to compute three indicators (root-mean-square resilience, root-mean-square reactivity and root-mean-square amplification envelope) of the response to perturbation for the studied ecosystem. Since the above-measured amounts cannot be obtained explicitly, we use numerical simulation to draw the changing figures within the appropriate parameter range. Then we obtain some conclusions by comparing the numerical results. When perturbing any populations, increasing the disturbance intensity will reduce the mean-square stable area of the system. Ecologists can manage the ecosystem, reduce losses and maximize benefits according to the numerical results of the root-mean-square amplification envelope.


2021 ◽  
Vol 53 ◽  
pp. 101089
Author(s):  
Niels De Troyer ◽  
Stijn Bruneel ◽  
Koen Lock ◽  
Mark S. Greener ◽  
Ennio Facq ◽  
...  

2021 ◽  
Vol 60 (42) ◽  
pp. 22892-22899
Author(s):  
Min Zheng ◽  
Ke Gao ◽  
Haitao Qin ◽  
Guigen Li ◽  
Hongjian Lu

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