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Persistence and extinction of a stochastic predator–prey model with modified Leslie–Gower and Holling-type II schemes
Advances in Difference Equations volume 2020, Article number: 179 (2020)
Abstract
In this paper, we use an Ornstein–Uhlenbeck process to describe the environmental stochasticity and propose a stochastic predator–prey model with modified Leslie–Gower and Holling-type II schemes. For each species, sharp sufficient conditions for persistence in the mean and extinction are respectively obtained. The results demonstrate that the persistence and extinction of the species have close relationships with the environmental stochasticity. In addition, the theoretical results are numerically illustrated by some simulations.
1 Introduction
The well-known predator–prey framework with modified Leslie–Gower and Holling-type II schemes (PPFMLHS) formulated by Aziz-Alaoui and Okiye [1] can be illustrated as follows:
where a, c, f and h are assumed to be positive constants. a means the intraspecific competition strength, c measures the per capita reduction rate, h characterises the safeguard of the environment and f possesses the like signification of c. In the past two decades, model (1) and its generalisations have been subjected to intensive research, and a mass of attractive features have been provided. For example, Aziz-Alaoui and Okiye [1] tested the boundedness and global stability of model (1); Guo and Song [2] dissected model (1) perturbed by the impulse; Abid et al. [3] probed into the optimal control of model (1); see [3–15] for more related outcomes.
The parameters in model (1) are hypothesised to be deterministic, which neglects the environmental perturbations, and hence model (1) cannot accurately depict the real situations. A mass of scholars (see [16–23]) introduced stochasticity into deterministic systems to dissect the functions of stochasticity on population dynamics. Particularly, under the hypothesis that the growth rates in model (1) are disturbed by the random perturbations with \(r_{i}\rightarrow r_{i}+\sigma _{i}\frac{\mathrm{d}B_{i}(t)}{dt}\), several authors (see [16–18, 20]) tested the following stochastic PPFMLHS:
where \(\sigma _{i}^{2}\) means the intensity of white noise, \(B_{i}(t)\) is a standard Brownian motion defined on \((\varOmega ,\mathcal{F}_{t}, P)\), a given complete probability space. Ji et al. [17, 18] probed into several dynamical characteristics of system (2) and offered extinct and persistent conditions for the system. Liu et al. [20] examined the persistence and extinction of model (2) with impulsive toxicant input.
Model (2) hypothesises that the growth rate in the random environments is linear with respect to the Gaussian white noise
Integrating on the interval \([0,T]\) results in
Therefore, the variance of the average per capita growth rate \(\overline{r}_{i}\) over an interval of length T tends to ∞ as \(T \rightarrow 0\). This is insufficient to describe the real situation. Several authors (see [24, 25]) have claimed that using the mean-reverting Ornstein–Uhlenbeck process is a more appropriate approach to incorporate the environmental perturbations. On account of this approach, one has
i.e.
where \(r_{i0}=\tilde{r}_{i}(0)\), \(\sigma _{i}(t)=\frac{\xi _{i}}{\sqrt{2\alpha _{i}}}\sqrt{1-e^{-2 \alpha _{i} t}}\), \(\alpha _{i}>0\) characterises the speed of reversion, \(\xi _{i}^{2}\) means the intensity of stochastic perturbations. We then derive the following stochastic PPFMLHS:
As far as we know, little research has been conducted to explore model (3). For this reason, we delve into the properties of model (3).
The arrangement of this paper is as follows. In Sect. 2, the persistence and extinction threshold for each population are proffered. In Sect. 3, some numerical simulations are performed to evidence the theoretical outcomes. In Sect. 4, a number of concluding remarks are put forward.
2 Main results
Define
Lemma 1
For arbitrary\((x(0),y(0))\in R_{+}^{2}\), model (3) possesses a unique solution\((x(t),y(t))\in R_{+}^{2}\)for all\(t\geq 0\)a.s. (almost surely).
Proof
Pay attention to the following system:
and \(u(0)=\ln {x(0)}\), \(v(0)=\ln {y(0)}\). Due to the fact that the coefficients of system (4) adhere to the Lipschitz condition, system (4) possesses a unique local solution \((u(t), v(t))\) on \([0, \tau _{*})\) (see Theorems 3.15–3.17 in [26]), where \(\tau _{*}\) means the explosion time. Then we can deduce from Itô’s formula that on \([0, \tau _{*})\) model (3) possesses a unique solution \((x(t),y(t))=(e^{u(t)},e^{v(t)})\) which is positive. Now we validate \(\tau _{*}= +\infty \). Focus on the following systems:
On the basis of the comparison theorem [27], for \(t\in [0,\tau _{*})\),
In accordance to Theorem 2.2 in [22],
and
Due to the fact that \(\varPhi (t)\), \(\psi (t)\), \(\varphi (t)\) are global, we can deduce that \(\tau _{*}=+\infty \). □
Lemma 2
([28])
Let\(\varGamma (t)\in C(\varOmega \times [0,+\infty ),[0,+\infty ))\).
- (I)
If one can find out three positive constantsκ, μand\(\mu _{0}\)such that, for all\(t \geq \kappa \), \(\ln {\varGamma (t)}\leq \mu {t}-\mu _{0}{\int _{0}^{t} \varGamma (s) \,\mathrm{d}s}+F(t)\), where\(F(t)/t\rightarrow 0\)as\(t\rightarrow +\infty \), then\(\limsup_{t \to +\infty }{t^{-1}\int _{0}^{t}\varGamma (s) \,\mathrm{d}s} \leq \frac{\mu }{\mu _{0}}\)a.s.
- (II)
If one can find out three positive constantsκ, μand\(\mu _{0}\)such that, for all\(t \geq \kappa \), \(\ln {\varGamma (t)}\geq \mu {t}-\mu _{0}{\int _{0}^{t}\varGamma (s) \,\mathrm{d}s}+F(t)\), where\(F(t)/t\rightarrow 0\)as\(t\rightarrow +\infty \), then\(\liminf_{t\to +\infty }{t^{-1}\int _{0}^{t} \varGamma (s) \,\mathrm{d}s} \geq \frac{\mu }{\mu _{0}}\)a.s.
Lemma 3
If\(\bar{b}_{1}>0\)and\(\bar{b}_{2}>0\), then\(\lim_{t\to +\infty }t^{-1}\ln {y(t)}=0\)a.s.
Proof
Choose sufficiently large T which fulfils that, for \(t \geq T\),
For \(t \geq T\), one can deduce from (9) that
where
It then follows from \(L_{1}(t)\geq 1\) that
where
Thus (11) implies that
where
For this reason,
We then deduce from \(\lim_{t\to +\infty }t^{-1}\int _{0}^{t} {\sigma _{i}(s)\,\mathrm{d}B_{i}(s)}=0\) (\(i=1, 2\)) that if \(\bar{b}_{2}>0\),
This, together with (12), indicates
Taking advantage of Itô’s formula to (6) deduces
namely,
For arbitrary \(\varepsilon >0\), one can find out \(T>0\) such that, for \(t\geq T\),
We then deduce from (13) that, for \(t\geq T\),
Choose \(0<\varepsilon <\bar{b}_{2}\). Making use of (I) and (II) in Lemma 2 yields that
We then deduce from the arbitrariness of ε that
which indicates that \(\lim_{t\to +\infty }{t^{-1}\ln {\psi (t)}}=0\) a.s. In accordance to (8),
□
Theorem 1
([28])
For model (3), the following conclusions hold:
- (i)
If\(\bar{b}_{1}<0\), \(\bar{b}_{2}<0\), then bothxandybecome extinct, i.e. \(\lim_{t\to +\infty }x(t)=0\), \(\lim_{t\to +\infty }y(t)=0\)a.s.
- (ii)
If\(\bar{b}_{1} < 0\), \(\bar{b}_{2} >0\), thenxbecomes extinct andyis persistent in the mean, i.e. \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t} y(s)\,\mathrm{d}s}=h\bar{b}_{2}/f\)a.s.
- (iii)
If\(\bar{b}_{1} > 0\), \(\bar{b}_{2}<0\), thenybecomes extinct andxis persistent in the mean, i.e. \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}x(s)\,\mathrm{d}s}= \bar{b}_{1}/a\)a.s.
- (iv)
When\(\bar{b}_{1}>0\), \(\bar{b}_{2}>0\), (a) if\(\bar{b}_{1}< c\bar{b}_{2}/f\), thenxbecomes extinct andyis persistent in the mean, i.e. \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}y(s)\,\mathrm{d}s}=h\bar{b}_{2}/f\)a.s.; (b) if\(\bar{b}_{1} >c\bar{b}_{2}/f\), then\(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t} x(s)\,\mathrm{d}s}=\bar{b}_{1}/a-c \bar{b}_{2}/(af)\), \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}{\frac{y(s)}{h+x(s)}} \,\mathrm{d}s}=\bar{b}_{2}/f\)a.s.
Proof
(i). Taking advantage of Itô’s formula to (3) results in
As a consequence,
We then deduce from (18) that, for sufficiently large t,
In accordance to \(\lim_{t\to +\infty }t^{-1}\int _{0}^{t}\sigma _{1}(s)\,\mathrm{d}B_{1}(s)=0\) and \(\bar{b}_{1}+\varepsilon <0\), we derive \(\lim_{t\to +\infty }x(t)=0\) a.s. Analogously, \(\bar{b}_{2}<0\) means that \(\lim_{t\to +\infty }y(t)=0\) a.s.
(ii). Note that \(\bar{b}_{1}<0\), hence (i) indicates that \(\lim_{t\to +\infty }x(t)=0\). As a result, for sufficiently large t,
Making use of Lemma 2 to (21) and (22) results in
We then deduce from the arbitrariness of ε that \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}y(s)\,\mathrm{d}s}=h\bar{b}_{2}/f\) a.s.
(iii). Since \(\bar{b}_{2}<0\), then analogous to the proof of (i), one can validate that \(\lim_{t\to +\infty }y(t)=0\). The proof of (iii) is analogous to that of (ii), thus is left out.
(iv). (a). Compute that \(\text{(18)}\times f-\text{(19)}\times c\),
On the basis of Lemma 3, for arbitrary \(\varepsilon >0\), we can find out \(T>0\) such that, for \(t\geq T\), \(ct^{-1}\ln {\frac{y(t)}{y(0)}}\leq \varepsilon /5\). For this reason,
As a result, for \(t\geq T\),
Choose \(0<\varepsilon < c\bar{b}_{2}-f\bar{b}_{1}\). Consequently, \(\lim_{t\to +\infty }x(t)=0\). The proof of
is analogous to that of (ii) and thereby is left out.
(b). On the basis of (19),
We then deduce from Lemma 3 and \(\lim_{t\to +\infty }t^{-1}\int _{0}^{t}\sigma _{2}(s)\,\mathrm{d}B_{2}(s)=0\) that
As a consequence, for any \(\varepsilon >0\), we can find out \(T>0\) such that, for \(t\geq T\),
Applying (26) to (18) gives that, for \(t\geq T\),
Choose \(0<\varepsilon <(\bar{b}_{1}-c\bar{b}_{2}/f)/2\). On the basis of Lemma 2,
We then deduce from the arbitrariness of ε that \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}x(s)\,\mathrm{d}s}=\bar{b}_{1}/a-c \bar{b}_{2}/(af)\). □
3 Discussions and numerical simulations
Now we test the functions of the mean-reverting Ornstein–Uhlenbeck process on the persistence and extinction of model (3). There are two key parameters in the Ornstein–Uhlenbeck process: the speed of reversion \(\alpha _{i}\) and the intensity of the perturbation \(\xi _{i}\). In light of Theorem 1, the persistence and extinction of system (3) are entirely dominated by the signs of \(\bar{b}_{1}\), \(\bar{b}_{2}\) and \(\bar{b}_{1}-c\bar{b}_{2}/f\). Clearly,
For this reason, with the rise of \(\alpha _{i}\) (respectively, \(\xi _{i}\)), species i tends to be persistent (respectively, extinct), \(i=1,2\). Furthermore, due to the fact that \(\frac{\partial (\bar{b}_{1}-c\bar{b}_{2}/f)}{\partial \alpha _{2}}<0\) (respectively, \(\frac{\partial (\bar{b}_{1}-c\bar{b}_{2}/f)}{\partial (\xi _{2}^{2})}>0\)), thus sufficiently large \(\alpha _{2}\) (respectively, \(\xi _{2}\)) could make the prey population extinct (respectively, persistent) provided \(\bar{b}_{1}>0\) and \(\bar{b}_{2}>0\).
Now we numerically validate the above outcomes (here we only provide the functions of \(\alpha _{i}\) since the functions of \(\xi _{i}\) can be proffered analogously). On the basis of the Milstein method offered in [29], model (3) can be discretized as follows:
where \(\xi ^{k}\), \(\eta ^{k}\), \(k = 1, 2, \ldots , K\), mean independent Gaussian random variables.
Choose \(r_{1}=0.6\), \(r_{2}=0.4\), \(r_{10}=0.3\), \(r_{20}=0.2\), \(\xi _{1}^{2}=1.43\), \(\xi _{2}^{2}=0.63\), \(a=0.4\), \(c=0.36\), \(f=0.25\), \(h=1\) (these and the following parameter values are hypothesised). Now, we let \(\alpha _{1}\) and \(\alpha _{2}\) vary.
Choose \(\alpha _{1} =0.55\), \(\alpha _{2}= 0.35\). Then \(\bar{b}_{1}=-0.05\), \(\bar{b}_{2}=-0.05\). On the basis of (i) in Theorem 1, both x and y become extinct. See Fig. 1.
Choose \(\alpha _{1}=0.55\), \(\alpha _{2}=0.525\). Then \(\bar{b}_{1}=-0.05\), \(\bar{b}_{2}=0.1\). On the basis of (ii) in Theorem 1, x becomes extinct and \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}y(s)\,\mathrm{d}s}=h\bar{b}_{1}/f=0.4\). See Fig. 2.
Choose \(\alpha _{1}=0.65\), \(\alpha _{2}=0.35\). Then \(\bar{b}_{1}=0.05\), \(\bar{b}_{2}=-0.05\). On the basis of (iii) in Theorem 1, y becomes extinct and \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}x(s)\,\mathrm{d}s}=\bar{b}_{1}/a=0.125\). See Fig. 3. Comparing Fig. 1 with Fig. 2, one could perceive that with the rise of \(\alpha _{2}\), the predator population inclines to be persistent. Analogously, comparing Fig. 1 with Fig. 3, one could perceive that with the rise of \(\alpha _{1}\), the prey population inclines to be persistent.
Choose \(\alpha _{1}=0.715\), \(\alpha _{2}=0.7875\). Then \(\bar{b}_{1}=0.1\), \(\bar{b}_{1}=0.2\), \(\bar{b}_{1}< c\bar{b}_{2}/f=0.288\). On the basis of (a) in Theorem 1, x becomes extinct and \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}y(s)\,\mathrm{d}s} =h\bar{b}_{2}/f=0.8\). See Fig. 4.
Choose \(\alpha _{1} =0.715\), \(\alpha _{2}= 0.45\). Then \(\bar{b}_{1}=0.1\), \(\bar{b}_{2}=0.05\), \(\bar{b}_{1}>c\bar{b}_{2}/f=0.072\). On the basis of (b) in Theorem 1, \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}x(s)\,\mathrm{d}s}=\bar{b}_{1}/a-c \bar{b}_{2}/(af)=0.07\). \(\lim_{t\to +\infty }{t^{-1}\int _{0}^{t}{\frac{y(s)}{h+x(s)}} \,\mathrm{d}s}=\bar{b}_{2}/f=0.2\). See Fig. 5. In comparison with Fig. 4, one could perceive that with the rise of \(\alpha _{2}\), the prey population inclines to become extinct.
4 Concluding remarks
In the present article, we took advantage of a mean-reverting Ornstein–Uhlenbeck process to portray the random perturbations in the environment and formulated a stochastic PPFMLHS which might be more appropriate than model (2). We offered the persistence-and-extinction threshold of the model and uncovered some significant functions of Ornstein–Uhlenbeck process: sufficiently large \(\alpha _{i}\) (the speed of reversion) could make species i persistent; furthermore, in some cases sufficiently large \(\alpha _{2}\) could make species 1 (the prey population) become extinct.
Several problems remain to be solved. First, the present article tests the predator–prey framework, it would be interesting to dissect the food-chain framework (see [30]). Second, the present article probed into the white noises, one could examine other random noises such as the telephone noise (see [31]), the Lévy noise (see [32]) etc. When the telephone noise is considered, model (3) is replaced with
where \(\lambda (t)\) is a Markov chain with finite states. When the Lévy noise is considered, model (3) is replaced with
where \(\mu (t^{-})\) means the left limit of \(\mu (t)\), Γ̃ is the compensating measure of a Poisson measure Γ, \(\varXi \subseteq (0,+\infty )\) adheres to \(\gamma (\varXi )<+\infty \), where γ is the characteristic measure of Γ̃. Finally, one could take the intraspecific competition of the predator population into account, which was neglected in model (3).
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Acknowledgements
The authors thank the editor and referees for their careful reading and valuable comments. The authors also thank Prof. Ronghua Tan for the writing instructions.
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ML thanks the National Natural Science Foundation of China (No. 11771174) and the Natural Science Foundation of Jiangsu Province, China (No. BK20170067), and ZJL thanks the National Natural Science Foundation of China (No. 11871201) and the Natural Science Foundation of Hubei Province, China (No. 2019CFB241). The above foundation items will be used to pay the publication charge.
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DXZ mainly finished the writing of the whole content of the paper. ML and ZJL mainly finished the establishment of model and development. All authors read and approved the final manuscript.
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Zhou, D., Liu, M. & Liu, Z. Persistence and extinction of a stochastic predator–prey model with modified Leslie–Gower and Holling-type II schemes. Adv Differ Equ 2020, 179 (2020). https://doi.org/10.1186/s13662-020-02642-9
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DOI: https://doi.org/10.1186/s13662-020-02642-9