Harvesting and predation occur through contact processes in which the rate
at which the managed (prey) population can be found depends on the
population size, usually saturating at high densities. Many models
incorporate saturation in this process without considering the effects
of the particular function used to describe it. We show that the sharpness
with which this saturation occurs has an important effect upon the resulting
population dynamics, with bistability (sometimes involving a stable
equilibrium and a stable limit cycle) occurring for saturation that is
any sharper than the commonly used Michaelis-Menten (Holling type II)
functional response. This sharpness threshold occurs across a wide range
of model types, from simple harvesting to density-dependent and
ratio-dependent predation.
Citation: Christopher M. Kribs-Zaleta. Sharpness of saturation in harvesting and predation[J]. Mathematical Biosciences and Engineering, 2009, 6(4): 719-742. doi: 10.3934/mbe.2009.6.719
Related Papers:
[1] |
Hongqiuxue Wu, Zhong Li, Mengxin He .
Dynamic analysis of a Leslie-Gower predator-prey model with the fear effect and nonlinear harvesting. Mathematical Biosciences and Engineering, 2023, 20(10): 18592-18629.
doi: 10.3934/mbe.2023825
|
[2] |
Rajalakshmi Manoharan, Reenu Rani, Ali Moussaoui .
Predator-prey dynamics with refuge, alternate food, and harvesting strategies in a patchy habitat. Mathematical Biosciences and Engineering, 2025, 22(4): 810-845.
doi: 10.3934/mbe.2025029
|
[3] |
Rongjie Yu, Hengguo Yu, Chuanjun Dai, Zengling Ma, Qi Wang, Min Zhao .
Bifurcation analysis of Leslie-Gower predator-prey system with harvesting and fear effect. Mathematical Biosciences and Engineering, 2023, 20(10): 18267-18300.
doi: 10.3934/mbe.2023812
|
[4] |
Peter A. Braza .
A dominant predator, a predator, and a prey. Mathematical Biosciences and Engineering, 2008, 5(1): 61-73.
doi: 10.3934/mbe.2008.5.61
|
[5] |
Eduardo Liz, Alfonso Ruiz-Herrera .
Delayed population models with Allee effects and exploitation. Mathematical Biosciences and Engineering, 2015, 12(1): 83-97.
doi: 10.3934/mbe.2015.12.83
|
[6] |
Christian Cortés García .
Bifurcations in a discontinuous Leslie-Gower model with harvesting and alternative food for predators and constant prey refuge at low density. Mathematical Biosciences and Engineering, 2022, 19(12): 14029-14055.
doi: 10.3934/mbe.2022653
|
[7] |
Yun Kang, Sourav Kumar Sasmal, Komi Messan .
A two-patch prey-predator model with predator dispersal driven by the predation strength. Mathematical Biosciences and Engineering, 2017, 14(4): 843-880.
doi: 10.3934/mbe.2017046
|
[8] |
Dongmei Wu, Hao Wang, Sanling Yuan .
Stochastic sensitivity analysis of noise-induced transitions in a predator-prey model with environmental toxins. Mathematical Biosciences and Engineering, 2019, 16(4): 2141-2153.
doi: 10.3934/mbe.2019104
|
[9] |
Roy Malka, Vered Rom-Kedar .
Bacteria--phagocyte dynamics,
axiomatic modelling and mass-action kinetics. Mathematical Biosciences and Engineering, 2011, 8(2): 475-502.
doi: 10.3934/mbe.2011.8.475
|
[10] |
Qizhen Xiao, Binxiang Dai .
Heteroclinic bifurcation for a general predator-prey model with Allee effect and state feedback impulsive control strategy. Mathematical Biosciences and Engineering, 2015, 12(5): 1065-1081.
doi: 10.3934/mbe.2015.12.1065
|
Abstract
Harvesting and predation occur through contact processes in which the rate
at which the managed (prey) population can be found depends on the
population size, usually saturating at high densities. Many models
incorporate saturation in this process without considering the effects
of the particular function used to describe it. We show that the sharpness
with which this saturation occurs has an important effect upon the resulting
population dynamics, with bistability (sometimes involving a stable
equilibrium and a stable limit cycle) occurring for saturation that is
any sharper than the commonly used Michaelis-Menten (Holling type II)
functional response. This sharpness threshold occurs across a wide range
of model types, from simple harvesting to density-dependent and
ratio-dependent predation.