Pages that link to "Item:Q4453592"
From MaRDI portal
The following pages link to Uniqueness of limit cycles in a predator-prey system with Holling-type functional response (Q4453592):
Displaying 19 items.
- A necessary and sufficient condition for global asymptotic stability of time-varying Lotka-Volterra predator-prey systems (Q499617) (← links)
- Dynamical and numerical analyses of a generalized food-chain model (Q1399716) (← links)
- Uniqueness of limit cycles of the predator-prey system with Beddington-DeAngelis functional response. (Q1426985) (← links)
- Uniqueness of limit cycles in predator--prey system: The role of weight functions (Q1869000) (← links)
- Attraction region for the classical Lotka-Volterra predator-prey model caused by impulsive effects (Q2037348) (← links)
- Uniform global asymptotic stability for nonautonomous nonlinear dynamical systems (Q2097571) (← links)
- Geometric criteria for the non-existence of cycles in predator-prey systems with group defense (Q2643260) (← links)
- Existence of limit cycle and center in two-species predator-prey system with Holling III functional response (Q2744548) (← links)
- Uniqueness of limit cycles in a harvested predator prey system with Holling type III functional response (Q2763776) (← links)
- Homoclinic orbits in predator-prey systems with a nonsmooth prey growth rate (Q3429196) (← links)
- (Q4796969) (← links)
- Non-algebraic limit cycles in Holling type III zooplankton-phytoplankton models (Q5027683) (← links)
- Global Stability and Canard Explosions of the Predator-Prey Model with the Sigmoid Functional Response (Q5085904) (← links)
- A predator-prey system with Holling-type functional response (Q5130858) (← links)
- Predator-Prey Interactions with Hunger Structure (Q5149214) (← links)
- (Q5296825) (← links)
- (Q5296988) (← links)
- Absence of limit cycles of a predator-prey system with a sigmoid functional response (Q5961681) (← links)
- Predator-prey model with sigmoid functional response (Q6558230) (← links)