Song Advances in Difference Equations (2021) 2021:189 https://doi.org/10.1186/s13662-021-03297-w
R E S E A R C H Open Access Dynamics of a stochastic population model with predation effects in polluted environments Guanghai Song1*
*Correspondence: [email protected] Abstract 1Huaiyin Normal University, Huaian, 223300, P.R. China The present paper puts forward and probes a stochastic single-species model with predation effect in a polluted environment. We propose a threshold between extermination and weak persistence of the species and provide sufficient conditions for the stochastic persistence of the species. In addition, we evaluate the growth rates of the solution. Theoretical findings are expounded by some numerical simulations. MSC: 60H10; 60H30; 92D25 Keywords: Predation effects; Random perturbations; Environmental pollution; Persistence
1 Introduction Environmental pollution because of industry, commerce, agriculture, and the rapid growth of human population has been increasingly prominent and has become an global problem. Pollutants have threatened the health of living organisms. For instance, Amoco Cadiz incident carried off more than 260 thousands tonnes of sea animals in one month [1]; Bhopal disaster killed about 15 thousands people and injured about 560 thousands people [2]; according to the United States Fish and Wildlife Service, pesticides carried off more than 72 million birds every year in US [3]. To probe the influence of pollutants on the evolution of populations, many mathemat- ical models have been put forward. In the 1980s, Hallam and his co-workers [4–6]first constructed a series of deterministic models with pollution and uncovered that environ- mental pollution has serious influence on the persistence and extermination of the species. These results were improved and extended [7–17]. Particularly, motivated by the fact that the evolution of populations often encounters environmental perturbations [18], several authors (see, e.g., [9, 12–17]) paid attention to stochastic population models with pollution and uncovered that environmental perturbations have vital functions on the persistence and extermination of the species. On the other hand, most populations have parasites and predators [19]. In general, these predation effects have negative functions on the growth of populations. Therefore we need
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to test population models with predation effects in polluted environments. However, little research has been conducted to exploit this problem (even for deterministic models). The objective of this paper is testing the above problem. We construct a population model with predation effects in polluted environments in Sect. 2 and testify that the model has a unique global positive solution in Sect. 3. Then we offer a threshold between exter- mination and weak persistence of the species and provide conditions under which the species is stochastically persistent in Sect. 4.InSect.5, we estimate the growth rates of the solution of the model. Finally, we give the conclusions of this paper and numerically expound the theoretical findings in Sect. 6.
2Themodel Without pollution and predation effects, suppose that the growth of the species follows the logistic role:
d (t) = (t) b – ξ (t) ,(1) dt where (t) is the population size at time t,andb >0andξ > 0 stand for the growth rate and the intraspecific competition rate, respectively. We consider the predation effects. In general, the predation effects saturate at high prey density and vanish quadratically as the prey density tends to zero [19]. Therefore it is rea- sonable to model the predation effects by the following function:
λ 2(t) , ρ2 + 2(t)
where λ is the upper limit of the predation effects, and ρ2 measures the saturate effect. Then model (1)isreplacedby
d (t) λ 2(t) = (t) b – ξ (t) – .(2) dt ρ2 + 2(t)
As said before, the evolution of populations often encounters environmental perturba- tions [18]. In general, we can take advantage of a color noise process to portray the envi- ronmental perturbations [20],anditissuitabletoutilizeaGaussianwhitenoiseprocessto depict a weakly correlated color noise [21]. Various ways were developed to incorporate the white noise into deterministic population models. A widely accepted way is to suppose that some parameters in the model are influenced by the white noise (see, e.g., [22–32]). Adopting these approaches,
˙ ˙ ˙ b → b + β1ψ1(t), –ξ → –ξ + β2ψ2(t), –λ → λ + β3ψ3(t),
where ψ1(t), ψ2(t), and ψ3(t) are independent standard Wiener processes defined on a
certain complete probability space (, F, {Ft}t≥0,P),andβi, i =1,2,3,standfortheinten- sities. As a result, model (2)isreplacedby λ (t) d (t)= (t) b – ξ (t)– dt ρ2 + 2(t) (3) β 2(t) + β (t)dψ (t)+β 2(t)dψ (t)+ 3 dψ (t). 1 1 2 2 ρ2 + 2(t) 3 Song Advances in Difference Equations (2021) 2021:189 Page 3 of 19
To characterize the influence of pollution, we hypothesize that the populations suck up the pollutants into their bodies [4–6]. Denote by T(t) the concentration of pollutants in the species, which can lead to a descent of the growth rate [4]: b → b – H1 T(t) ,
where H1(T) is a positive continuous increasing function of T. Accordingly, model (3)is replaced by λ (t) d (t)= (t) b – H T(t) – ξ (t)– dt 1 ρ2 + 2(t) (4) β 2(t) + β (t)dψ (t)+β 2(t)dψ (t)+ 3 dψ (t). 1 1 2 2 ρ2 + 2(t) 3
To depict the pollutants in the species, we pay attention to the following equation:
dT(t) = H T (t) – H T(t) ,(5) dt 2 e 3
where Te(t) represents the concentration of pollutants in the environment, H2(Te(t)) > 0
characterizes the suck up of pollutants from the environment, H3(T(t)) > 0 measures the 1 1 loss of pollutants because of excretion and detoxication. Both H2 ∈ C and H3 ∈ C are increasing functions.
Finally, we portray the changes of Te(t). Denote by u(t) a continuous and bounded func- tion of t, the input of pollutants from the outside of the environment. Suppose that the
changes of Te(t) are governed by the following equation:
dT (t) e = u(t)–H T (t) ,(6) dt 4 e
1 where H4 ∈ C , measuring the loss of the pollutants from the environment, is an increasing
positive function of Te. According to (4)–(6), we derive the following model: ⎧ ⎪d (t)= (t)(b – H (T(t)) – ξ (t)– λ (t) )dt ⎪ 1 ρ2+ 2(t) ⎪ 2 ⎨ 2 β3 (t) + β1 (t)dψ1(t)+β2 (t)dψ2(t)+ dψ3(t), ρ2+ 2(t) (7) ⎪ dT(t) ⎪ dt = H2(Te(t)) – H3(T(t)), ⎩⎪ dTe(t) dt = u(t)–H4(Te(t)).
The objectives of this paper is probing some dynamical properties of (t). Note that the last two equations in model (7) do not depend on (t), and they have a unique solution
(T(t), Te(t)) for certain initial value. As a result, from now on we concentrate on Eq. (4).
3 The existence and uniqueness of the solution Theorem 1 For any initial value (0) > 0, Eq.(4) possesses a unique global positive solu- tion (t) almost surely (a.s.). Song Advances in Difference Equations (2021) 2021:189 Page 4 of 19
Proof We first concentrate on the equation β2 λex(t) β2 β2e2x(t) dx(t)= b – H T(t) – 1 – ξex(t) – – 2 e2x(t) – 3 dt 1 2 ρ2 + e2x(t) 2 2(ρ2 + e2x(t))2 (8) β ex(t) + β dψ (t)+β ex(t) dψ (t)+ 3 dψ (t) 1 1 2 2 ρ2 + e2x(t) 3
with x(0) = ln (0). By the locally Lipschitz continuity of the coefficients in Eq. (8)we
deduce that Eq. (8)possessesauniquesolutionon[0,τe), where τe ≤ +∞. It then follows from Itô’s formula (see [33], p. 32, Theorem 6.2) that (t)=ex(t) istheuniquepositive solution of (4).
Now we testify that τe =+∞.Letm0 be a positive constant such that m0 > (0). For each integer m,define τm = inf t ∈ [0, τe): (t) ≥ m .
Let τ∞ = limm→+∞ τm. We can deduce that τ∞ ≤ τe.Ifτe <+∞, then we can find out con- stants Tˆ >0and ∈ (0, 1) such that
ˆ P{τ∞ ≤ T} > .
It then follows that we can find out an integer m1 ≥ m0 such that for any m ≥ m1,
P{m}≥ ,(9)
ˆ where m = {ω : τm ≤ T}.Define
γ W1( )= , >0,0<γ <1.
Then we deduce by Itô’s formula that
dW1( ) λ γ –1 γ –1 (γ –1)β2 2 = γ γ b – H T(t) – ξ – + β2 + β2 2 + 3 dt 1 ρ2 + 2 2 1 2 2 2(ρ2 + 2)2 γβ γ +1 + γβ γ dψ (t)+γβ γ +1 dψ (t)+ 3 dψ (t) 1 1 2 2 ρ2 + 2 3 β ≤ γ bW ( )dt + γ W ( ) β dψ (t)+β dψ (t)+ 3 dψ (t) . 1 1 1 1 2 2 ρ2 + 2 3
Accordingly,