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The recent focus in the fields of biology and ecology has centered on the significant attention given to the mathematical modeling and analyzing the spatiotemporal population distribution among species engaged in interactions. This paper explores the dynamics of the temporal and spatiotemporal delayed Bazykin-type prey–predator model, incorporating fear and its carryover effect. In our model, we incorporated a functional response of the Holling-type II. In the temporal model, a detailed dynamic analysis was carried out, investigating the positivity and boundedness of solutions, establishing the uniqueness and existence of positive interior equilibria, and examining both local and global stability. Additionally, we explored the presence of saddle-node, transcritical, and Hopf bifurcations varying attack rate parameter. The delayed system shows highly periodic behavior. Additionally, for the spatiotemporal model, we provide a complete analysis of local and global stability, and we derive the conditions for the existence of Turing instability for both self-diffusion and cross-diffusion, respectively. The two-dimensional diffusive model is further discussed, highlighting various Turing patterns, including holes, stripes, and hot and cold spots, along with their biological significance. Numerical simulations are executed to validate the analytical findings in both temporal and spatiotemporal models. [ABSTRACT FROM AUTHOR]

This paper presents the temporal and spatiotemporal dynamics of a delayed prey–predator system with a variable carrying capacity. Prey and predator interact via a Holling type-II functional response. A detailed dynamical analysis, including well-posedness and the possibility of coexistence equilibria, has been performed for the temporal system. Local and global stability behavior of the co-existence equilibrium is discussed. Bistability behavior between two coexistence equilibria is demonstrated. The system undergoes a Hopf bifurcation with respect to the parameter β , which affects the carrying capacity of the prey species. The delayed system exhibits chaotic behavior. A maximal Lyapunov exponent and sensitivity analysis are done to confirm the chaotic dynamics. In the spatiotemporal system, the conditions for Turing instability are derived. Furthermore, we analyzed the Turing pattern formation for different diffusivity coefficients for a two-dimensional spatial domain. Moreover, we investigated the spatiotemporal dynamics incorporating two discrete delays. The effect of the delay parameters in the transition of the Turing patterns is depicted. Various Turing patterns, such as hot-spot, coldspot, patchy, and labyrinth, are obtained in the case of a two-dimensional spatial domain. This study shows that the parameter β and the delay parameters significantly instigate the intriguing system dynamics and provide new insights into population dynamics. Furthermore, extensive numerical simulations are carried out to validate the analytical findings. The findings in this article may help evaluate the biological revelations obtained from research on interactions between the species. [ABSTRACT FROM AUTHOR]

The present work highlights the reverse side of the same ecological coin by considering the counter-attack of prey on immature predators. We assume that the birth rate of prey is affected by the fear of adult predators and its carry-over effects (COEs). Next, we introduce two discrete delays to show time lag due to COEs and fear-response. We observe that the existence of a positive equilibrium point and the stability of the prey-only state is independent of fear and COEs. Furthermore, the necessary condition for the co-existence of all three species is determined. Our system experiences several local and global bifurcations, like, Hopf, saddle-node, transcritical, and homoclinic bifurcation. The simultaneous variation in the attack rate of prey and predator results in the Bogdanov–Takens bifurcation. Our numerical results explain the paradox of enrichment, chaos, and bi-stability of node-focus and node-cycle types. The system, with and without delay, is analyzed theoretically and numerically. Using the normal form method and center manifold theorem, the conditions for stability and direction of Hopf-bifurcation are also derived. The cascade of predator attacks, prey counter-attacks, and predator defense exhibit intricate dynamics, which sheds light on ecological harmony. [ABSTRACT FROM AUTHOR]

This study presents a qualitative analysis of a modified Leslie–Gower prey–predator model with fear effect and prey refuge in the presence of diffusion and time delay. For the non-delayed temporal system, we examined the dissipativeness and persistence of the solutions. The existence of equilibria and stability analysis is performed to comprehend the complex behavior of the proposed model. Bifurcation of codimension-1, such as Hopf-bifurcation and saddle-node, is investigated. In addition, it is observed that increasing the strength of fear may induce periodic oscillations, and a higher value of fear may lead to the extinction of prey species. The system shows a bistability attribute involving two stable equilibria. The impact of providing spatial refuge to the prey population is also examined. We noticed that prey refuge benefits both species up to a specific threshold value beyond which it turns detrimental to predator species. For the non-spatial delayed system, the direction and stability of Hopf-bifurcation are investigated with the help of the center manifold theorem and normal form theory. We noticed that increasing the delay parameter may destabilize the system by producing periodic oscillations. For the spatiotemporal system, we derived the analytical conditions for Turing instability. We investigated the pattern dynamics driven by self-diffusion. The biological significance of various Turing patterns, such as cold spots, stripes, hot spots, and organic labyrinth, is examined. We analyzed the criterion for Hopf-bifurcation for the delayed spatiotemporal system. The impact of fear response delay on spatial patterns is investigated. Numerical simulations are illustrated to corroborate the analytical findings. [ABSTRACT FROM AUTHOR]

Phytoplankton–zooplankton interaction is a topic of high interest among the interrelationships related to marine habitats. In the present manuscript, we attempt to study the dynamics of a three-dimensional system with three types of plankton: non-toxic phytoplankton, toxic producing phytoplankton, and zooplankton. We assume that both non-toxic and toxic phytoplankton are consumed by zooplankton via Beddington–DeAngelis and general Holling type-IV responses, respectively. We also incorporate gestation delay and toxic liberation delay in zooplankton's interactions with non-toxic and toxic phytoplankton correspondingly. First, we have studied the well-posedness of the system. Then, we analyze all the possible equilibrium points and their local and global asymptotic behavior. Furthermore, we assessed the conditions for the occurrence of Hopf-bifurcation and transcritical bifurcation. Using the normal form method and center manifold theorem, the conditions for stability and direction of Hopf-bifurcation are also studied. Various time-series, phase portraits, and bifurcation diagrams are plotted to confirm our theoretical findings. From the numerical simulation, we observe that a limited increase in inhibitory effect of toxic phytoplankton against zooplankton can support zooplankton's growth, and rising predator's interference can also boost zooplankton expansion in contrast to the nature of Holling type IV and Beddington–DeAngelis responses. Next, we notice that on variation of toxic liberation delay, the delayed system switches its stability multiple times and becomes chaotic. Furthermore, we draw the Poincaré section and evaluate the maximum Lyapunov exponent in order to verify the delayed system's chaotic nature. Results presented in this article might be helpful to interpret biological insights into phytoplankton–zooplankton interactions. [ABSTRACT FROM AUTHOR]

In our ecological system, prey species can defend themselves by casting strong and effective defenses against predators, which can slow down the growth rate of prey. Predator has more at stake when pursuing a deadly prey than just the chance of missing the meal. Prey have to "trade off" between reproduction rate and safety and whereas, predator have to "trade off" between food and safety. In this article, we investigate the trade-off dynamics of both predator and prey when the predator attacks a dangerous prey. We propose a two-dimensional prey and predator model considering the logistic growth rate of prey and Holling type-2 functional response to reflect predator's successful attacks. We examine the cost of fear to reflect the trade-off dynamics of prey, and we modify the predator's mortality rate by introducing a new function that reflects the potential loss of predator as a result of an encounter with dangerous prey. We demonstrated that our model displays bi-stability and undergoes transcritical bifurcation, saddle node bifurcation, Hopf bifurcation, and Bogdanov–Taken bifurcations. To explore the intriguing trade-off dynamics of both prey and predator population, we investigate the effects of our critical parameters on both population and observed that either each population vanishes simultaneously or the predator vanishes depending on the value of the handling time of the predator. We determined the handling time threshold upon which dynamics shift, demonstrating the illustration of how predators risk their own health from hazardous prey for food. We have conducted a sensitivity analysis with regard to each parameter. We further enhanced our model by including fear response delay and gestation delay. Our delay differential equation system is chaotic in terms of fear response delay, which is evidenced by the positivity of maximum Lyapunov exponent. We have used numerical analysis to verify our theoretical conclusions, which include the influence of vital parameters on our model through bifurcation analysis. In addition, we used numerical simulations to showcase the bistability between co-existence equilibrium and prey only equilibrium with their basins of attraction. The results that are reported in this article might be useful in interpreting the biological insights gained from studying the interactions between prey and predator. [ABSTRACT FROM AUTHOR]

In this investigation, we construct a predator–prey model that distinguishes between immature and mature prey, highlighting group defense strategies within the mature prey. First, we embark on exploring the positivity and boundedness of the solution, unraveling sustainable equilibrium points, and deducing their stability conditions. Upon further investigation, we observe that the system exhibits diverse bifurcations, including Hopf, saddle-node, transcritical, generalized Hopf, cusp, and Bogdanov–Takens bifurcations. The results reveal that heightened fear decreases mature prey density, potentially causing prey extinction beyond a certain threshold. Increased maturation rates lead to the coexistence of immature and mature prey populations and higher predator density. Stronger group defense boosts mature prey density, while weaker defense results in weak persistence. Lower values of the maturation rate of prey and the decline rate of predators sustain only the predator population, reliant on resources other than focal prey. Furthermore, our model demonstrates intriguing and diverse dynamical phenomena, including various forms of bistability across distinct bi-parameter planes. We also explore the dynamics of a related nonautonomous system, where certain parameters are considered to vary with time. In the seasonally forced model, we set out to define criteria regarding the existence and stability of positive periodic solutions. Numerical investigations into the seasonally forced model uncover a spectrum of dynamics, ranging from simple periodic solutions to higher periodicities, bursting patterns, and chaotic behavior. [ABSTRACT FROM AUTHOR]

The interplay of phytoplankton, zooplankton, and fish is one of the most important aspects of the aquatic environment. In this paper, we propose to explore the dynamics of a phytoplankton–zooplankton–fish system, with fear-induced birth rate reduction in the middle predator by the top predator and an additional food source for the top predator fish. Phytoplankton–zooplankton and zooplankton–fish interactions are handled using Holling type IV and II responses, respectively. First, we prove the well-posedness of the system, followed by results related to the existence of possible equilibrium points. Conditions under which a different number of interior equilibria exist are also derived here. We also show this existence numerically by varying the intrinsic growth rate of phytoplankton species, which demonstrates the model's vibrant nature from a mathematical point of view. Furthermore, we performed the local and global stability analysis around the above equilibrium points, and the transversality conditions for the occurrence of Hopf bifurcations and transcritical bifurcations are established. We observe numerically that for low levels of fear, the system behaves chaotically, and as we increase the fear parameter, the solution approaches a stable equilibrium by the route of period-halving. The chaotic behavior of the system at low levels of fear can also be controlled by increasing the quality of additional food. To corroborate our findings, we constructed several phase portraits, time-series graphs, and one- and two-parametric bifurcation diagrams. The computation of the largest Lyapunov exponent and a sketch of Poincaré maps verify the chaotic character of the proposed system. On varying the parametric values, the system exhibits phenomena like multistability and the enrichment paradox, which are the basic qualities of non-linear models. Thus, the current study can also help ecologists to estimate the parameters to study and obtain such important findings related to non-linear PZF systems. Therefore, from a biological and mathematical perspective, the analysis and the corresponding results of this article appear to be rich and interesting. [ABSTRACT FROM AUTHOR]