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1.
霍丽慧  赵惠燕  郑立飞  吴养会 《生态学报》2010,30(20):5702-5708
现有的具有年龄结构的捕食-食饵模型总是假设只有成年捕食者捕食猎物,这与实际情况不符。建立了一个幼年捕食者捕食食饵的具有年龄结构的食蚜蝇-蚜虫模型,应用微分方程定性理论,讨论了系统平衡点及其稳定性:其中平衡点E1(0,0,0)为不稳定的;满足一定条件时,边界平衡点E2(K,0,0)及正平衡点E3(x*,y1*,y2*)为局部渐近稳定的;且应用一致持续生存理论得到了系统永久持续生存的条件,为有害生物综合治理提供了理论依据。  相似文献   

2.
刘志广 《生态学报》2018,38(8):2958-2964
建立了一个显式含有空间庇护所的两斑块Leslie-Gower捕食者-食饵系统。假设只有食饵种群在斑块间以常数迁移率迁移,且在每个斑块上食饵间的迁移比局部捕食者-食饵相互作用发生的时间尺度要快。利用两个时间尺度,可以构建用来描述所有斑块总的食饵和捕食者密度的综合系统。数学分析表明,在一定条件下,存在唯一的正平衡点,并且此平衡点全局稳定。进一步,捕食者的数量随着食饵庇护所数量增加而降低;在一定条件下,食饵的数量随着食饵庇护所数量增加先增加后降低,在足够强的庇护所强度下,两物种出现灭绝。对比以往研究,利用显式含有和隐含空间庇护所的数学模型所得结论不一致,这意味着在研究庇护所对捕食系统种群动态影响时,空间结构可能起着重要作用。  相似文献   

3.
We present a conceptual mathematical model of the dynamics of a spatially heterogeneous population system whose prototype is the fish community of Lake Syamozero. Analysis of the solutions of this model is used to demonstrate that interactions between the predator and prey populations in two neighboring biotopes (the pelagic and coastal zones) may result in either undamped oscillations or steady states of the population sizes. The model population densities are of the same order of magnitude as the values obtained in long-term observations of the Syamozero biota. It is also demonstrated that the transition to steady states may be accompanied by long-term (dozens or hundreds of years) damped oscillations of the prey and predator population densities. Under natural conditions, long transitional periods may prevent fish communities from reaching stationary modes.  相似文献   

4.
The current paper deals with the mathematical models of predator–prey system where a transmissible disease spreads among the predator species only. Four mathematical models are proposed and analysed with several popular predator functional responses in order to show the influence of functional response on eco-epidemic models. The existence, boundedness, uniqueness of solutions of all the models are established. Mathematical analysis including stability and bifurcation are observed. Comparison among the results of these models allows the general conclusion that relevant behaviour of the eco-epidemic predator–prey system, including switching of stability, extinction, persistence and oscillations for any species depends on four important parameters viz. the rate of infection, predator interspecies competition and the attack rate on susceptible predator. The paper ends with a discussion of the biological implications of the analytical and numerical results.  相似文献   

5.
1. Current formulations of functional responses assume that the prey is homogeneous and independent of intraspecific processes. Most prey populations consist of different coexisting size classes that often engage in asymmetrical intraspecific interactions, including cannibalism, which can lead to nonlinear interaction effects. This may be important as the size structure with the prey could alter the overall density-dependent predation rates. 2. In a field experiment with damselfly and dragonfly larvae, 16 treatments manipulated the density of a small prey stage, the presence of large conspecific prey and the presence of heterospecific predators. 3. Size structure in the prey (i.e. when both prey stages were present) decreased the impact of the predator on overall prey mortality by 25-48% at mid and high prey densities, possibly due to density-dependent size-structured cannibalism in the prey. The predation rates on small prey stages were determined by the interaction of large prey and predators. Predation rates increased with prey density in the absence of large prey, but predation rates were constant across densities when large conspecifics were present. 4. The functional response for unstructured prey followed a Holling type III model, but the predation rate for size-structured prey was completely different and followed a complex pattern that could not be explained with any standard functional response. 5. Using additional laboratory experiments, a mortality model was developed and parameterized. It showed that the overall prey mortality of size-structured prey can be adequately predicted with a composite functional response model that modelled the individual functional responses of each prey stage separately and accounted for their cannibalistic interaction. 6. Thus, treating a prey population as a homogeneous entity will lead to erroneous predictions in most real-world food webs. However, if we account for the effects of size structure and the intraspecific interactions on functional responses by treating size classes as different functional groups, it is possible to reliably predict the dynamics of size-structured predator-prey systems.  相似文献   

6.
The product of Xer recombination at directly repeated psi sites on a circular unknotted DNA molecule is a right-hand four-noded catenane. Here, we use tangle equations to analyze the topological changes associated with Xer recombination at psi. This mathematical method allows computation of all possible topological pathways consistent with the experimental data. We give a rigorous mathematical proof that, under reasonable biological assumptions, there are only three solutions to the tangle equations. One of the solutions corresponds to a synaptic complex with antiparallel alignment of recombination core sites, the other two correspond to parallel alignment of cores. We show that all three solutions can be unified into a single three-dimensional model for Xer recombination. Thus the three distinct mathematical solutions do not necessarily represent distinct three-dimensional pathways, and in this case the three distinct tangle solutions are different planar projections of the same three-dimensional configuration.  相似文献   

7.
We consider a biological economic model based on prey-predator interactions to study the dynamical behaviour of a fishery resource system consisting of one prey and two predators surviving on the same prey. The mathematical model is a set of first order non-linear differential equations in three variables with the population densities of one prey and the two predators. All the possible equilibrium points of the model are identified, where the local and global stabilities are investigated. Biological and bionomical equilibriums of the system are also derived. We have analysed the population intensities of fluctuations i.e., variances around the positive equilibrium due to noise with incorporation of a constant delay leading to chaos, and lastly have investigated the stability and chaotic phenomena with a computer simulation.  相似文献   

8.
The influence of a resource subsidy on predator–prey interactions is examined using a mathematical model. The model arises from the study of a biological system involving arctic foxes (predator), lemmings (prey), and seal carcasses (subsidy). In one version of the model, the predator, prey and subsidy all occur in the same location; in a second version, the predator moves between two patches, one containing only the prey and the other containing only the subsidy. Criteria for feasibility and stability of the different equilibrium states are studied both analytically and numerically. At small subsidy input rates, there is a minimum prey carrying capacity needed to support both predator and prey. At intermediate subsidy input rates, the predator and prey can always coexist. At high subsidy input rates, the prey cannot persist even at high carrying capacities. As predator movement increases, the dynamic stability of the predator–prey-subsidy interactions also increases.  相似文献   

9.
With a series of mathematical models, we explore impacts of predation on a prey population structured into two age classes, juveniles and adults, assuming generalist, age-specific predators. Predation on any age class is either absent, or represented by types II or III functional responses, in various combinations. We look for Allee effects or more generally for multiple stable steady states in the prey population. One of our key findings is the occurrence of a predator pit (low-density ??refuge?? state of prey induced by predation; the chance of escaping predation thus increases both below and above an intermediate prey density) when only one age class is consumed and predators use a type II functional response ??this scenario is known to occur for an unstructured prey consumed via a type III functional response and can never occur for an unstructured prey consumed via a type II one. In the case where both age classes are consumed by type II generalist predators, an Allee effect occurs frequently, but some parameters give also rise to a predator pit and even three stable equilibria (one extinction equilibrium and two positive ones??Allee effect and predator pit combined). Multiple positive stable equilibria are common if one age class is consumed via a type II functional response and the other via a type III functional response??here, in addition to the behaviours mentioned above one may even observe three stable positive equilibria????double?? predator pit. Some of these results are discussed from the perspective of population management.  相似文献   

10.
We propose and analyze a simple mathematical model for susceptible prey (S)–infected prey (I)–predator (P) interaction, where the susceptible prey population (S) is infected directly from external sources as well as through contact with infected class (I) and the predator completely avoids consuming the infected prey. The model is analyzed to obtain different thresholds of the key parameters under which the system exhibits stability around the biologically feasible equilibria. Through numerical simulations we display the effects of external infection and the infection through contact on the system dynamics in the absence as well as in the presence of the predator. We compare the system dynamics when infection occurs only through contact, with that when it occurs through contact and external sources. Our analysis demonstrates that under a disease-selective predation, stability and oscillations of the system is determined by two key parameters: the external infection rate and the force of infection through contact. Due to the introduction of external infection, the predator and the prey population show limit-cycle oscillations over a range parametric values. We suggest that while predicting the dynamics of such an eco-epidemiological system, the modes of infection and the infection rates might be carefully investigated.  相似文献   

11.
Studies on the evolution of aposematic coloration (prey coloration advertising for unpalatability) have mainly focused on predator psychology in simplified single-prey species systems. We chose, instead, to model population dynamics on the community level. We studied the invasion by an aposematic phenotype in the presence and absence of another prey species. The single-prey and two-prey models differed in two major ways. First, with two prey species the invasion was possible only with a weak aposematic signal, whereas with a single prey species there was no such an upper limit for signal strength. Second, with a single prey species, increase of the aposematic phenotype always resulted in rapid extinction of the predator. Resource value and growth rate of the alternative prey species affected the invasion. These results suggest that community structure is an important determinant of the conditions for invasion of aposematism, and may have contributed to its initial evolution.  相似文献   

12.
Intraguild predation (IGP) is a combination of competition and predation which is the most basic system in food webs that contains three species where two species that are involved in a predator/prey relationship are also competing for a shared resource or prey. We formulate two intraguild predation (IGP: resource, IG prey and IG predator) models: one has generalist predator while the other one has specialist predator. Both models have Holling-Type I functional response between resource-IG prey and resource-IG predator; Holling-Type III functional response between IG prey and IG predator. We provide sufficient conditions of the persistence and extinction of all possible scenarios for these two models, which give us a complete picture on their global dynamics. In addition, we show that both IGP models can have multiple interior equilibria under certain parameters range. These analytical results indicate that IGP model with generalist predator has “top down” regulation by comparing to IGP model with specialist predator. Our analysis and numerical simulations suggest that: (1) Both IGP models can have multiple attractors with complicated dynamical patterns; (2) Only IGP model with specialist predator can have both boundary attractor and interior attractor, i.e., whether the system has the extinction of one species or the coexistence of three species depending on initial conditions; (3) IGP model with generalist predator is prone to have coexistence of three species.  相似文献   

13.
We consider a predator-prey model in a two-patch environment and assume that migration between patches is faster than prey growth, predator mortality and predator-prey interactions. Prey (resp. predator) migration rates are considered to be predator (resp. prey) density-dependent. Prey leave a patch at a migration rate proportional to the local predator density. Predators leave a patch at a migration rate inversely proportional to local prey population density. Taking advantage of the two different time scales, we use aggregation methods to obtain a reduced (aggregated) model governing the total prey and predator densities. First, we show that for a large class of density-dependent migration rules for predators and prey there exists a unique and stable equilibrium for migration. Second, a numerical bifurcation analysis is presented. We show that bifurcation diagrams obtained from the complete and aggregated models are consistent with each other for reasonable values of the ratio between the two time scales, fast for migration and slow for local demography. Our results show that, under some particular conditions, the density dependence of migrations can generate a limit cycle. Also a co-dim two Bautin bifurcation point is observed in some range of migration parameters and this implies that bistability of an equilibrium and limit cycle is possible.  相似文献   

14.
Genetically engineered baculoviruses, relative to their wild-type progenitors, have successfully improved the time-to-kill of these arthropod-specific biopesticides. Beneficial arthropods that prey on targeted pest insects are likely the first nontarget organisms to be adversely affected by the applications of such biopesticides. The goals of this project were to assess potential risks of the recombinant baculoviruses on Solenopsis invicta, Geocoris punctipes, and Hippodamia convergens, all of which are common predators of heliothines in Texas cotton. Four recombinant Autographa californica nuclear polyhedrosis viruses (AcNPV), one Helicoverpa zea nuclear polyhedrosis virus (HzNPV), and two corresponding wild-type NPVs were used in this risk assessment study. Risks associated with these baculoviruses were determined by possible shifts in predator life history traits (rate of food consumption, travel speed, fecundity, and survival) when fed prey infected with recombinant viruses compared to prey infected with wild-type viruses or to healthy prey. We also tested for possible transmission of these viruses by predators using the polymerase chain reaction (PCR). No significant shifts in life history characteristics were detected in predators fed Heliothis virescens larvae infected with any of the seven viruses. Viral DNA was discovered using PCR in 2.3% of fire ant workers, but not from any of the queens or eggs. In G. punctipes, 13.4% of adults and 0.5% of eggs scored positive for viruses. Twelve percent of H. convergens adults were found PCR positive. Residency in all three predators tested provides a pathway which could increase the persistence of recombinant viral particles in the environment and thus may produce an indeterminable amount of risk associated with their inadvertent movement.  相似文献   

15.
A four-dimensional food-web system consisting of a bottom prey, two middle predators and a generalist predator has been developed with modified functional response. The system is well posed and dissipative. Some results on uniform persistence have been developed. The dynamics of the system is found to be chaotic for certain choice of parameters. The coexistence of all four species is possible in the form of periodic orbits/strange attractors for suitably chosen set of parameters.  相似文献   

16.
A refuge model is developed for a single predator species and either one or two prey species where no predators are present in the prey refuge. An individual’s fitness depends on its strategy choice or ecotype (predators decide which prey species to pursue and prey decide what proportion of their time to spend in the refuge) as well as on the population sizes of all three species. It is shown that, when there is a single prey species with a refuge or two prey species with no refuge compete only indirectly (i.e. there is only apparent competition between prey species), that stable resident systems where all individuals in each species have the same ecotype cannot be destabilized by the introduction of mutant ecotypes that are initially selectively neutral. In game-theoretic terms, this means that stable monomorphic resident systems, with ecotypes given by a Nash equilibrium, are both ecologically and evolutionarily stable. However, we show that this is no longer the case when the two indirectly-competing prey species have a refuge. This illustrates theoretically that two ecological factors, that are separately stabilizing (apparent competition and refuge use), may have a combined destabilizing effect from the evolutionary perspective. These results generalize the concept of an evolutionarily stable strategy (ESS) to models in evolutionary ecology. Several biological examples of predator–prey systems are discussed from this perspective.  相似文献   

17.
1. Population models based on Lotka–Volterra-type differential equations with logistic prey were made for a simple stream community including two stonefly prey Leuctra nigra Olivier and Nemurella pictetii Klàpalek, and two predators, the caddisfly Plectrocnemia conspersa (Curtis) and the alderfly Sialis fuliginosa Pictet. In order to assess the importance of predation in this system, we constructed both an explicit four-species model and a simplified model with two functional groups which was more amenable to analytical treatment.
2. The models were parameterized using new data on adult emergence and recruitment combined with previously published data on larval densities and prey uptake. The models were falsified if parameterizations led either to negative prey carrying capacities or to unstable dynamics.
3. Both the functional group and four-species models predict asymptotically stable interactions, with feasible carrying capacities. The models are consistent in predicting that the observed prey are in excess of 70% of their carrying capacities. The four-species model indicates that predation impact is not evenly shared between the two prey, with L. nigra being depressed further from its carrying capacity than N. pictetii .
4. Sensitivity analysis shows that the results of the full four-species model remain very robust to realistic levels of stochastic variation in the input data.
5. The four-species model is used to predict the outcome of an ongoing large-scale field experiment involving the transfer of all S. fuliginosa eggs from one stretch of the stream to another. Although the equilibrial prey populations are barely affected by the manipulation, the model predicts marked transient prey-release and prey-depression of L. nigra in the predator addition and removal areas, respectively.  相似文献   

18.
19.
Predator foraging facilitation may strongly influence the dynamics of a predator–prey system. This behavioral pattern is well-observed in real life interactions, but less is known about its possible impacts on the predator–prey dynamics. In this paper we analyze a modified Rosenzweig–MacArthur model, where a predator-dependent family of functions describing predator foraging facilitation is introduced into the Holling type II functional response. As the general assumption of foraging facilitation is that higher predator densities give rise to an increased foraging efficiency, we model predator facilitation with an increasing encounter rate function. Using the tools of bifurcation analysis we describe all the nonlinear phenomena that occur in the system provoked by foraging facilitation, these include the fold, Hopf, transcritial, homoclinic and Bogdanov–Takens bifurcation. We show that foraging facilitation can stabilize the coexistence in the predator–prey system for specific rates, but in most of the cases it can have fatal consequences for the predators themselves.  相似文献   

20.
1. We examined the effect of different periods of prior starvation(from 30 min to 16 h) on the prey capture behaviour, and functional and numerical responses of the predatory rotifer Asplanchna sieboldi using the rotifer Brachionus calyciflorus as prey.
2. Feeding activity (i.e. encounter, attack, capture and ingestion) by Asplanchna increased significantly with increasing prey densities from 2 to 16 mL−−1 and with increasing prior starvation periods from 0.5 to 8 h.
3.  Asplanchna sieboldi showed a type II functional response at all the prior starvation periods tested. The asymptotic prey density was highest after 8 h of starvation.
4. The instantaneous population growth rate of A. sieboldi ranged from 0.089 ± 0.044 (when starved for 8 h in every 24 h and at a prey density of 2 individuals mL−−1 for the other 16 h) to 1.015 ± 0.142 in the control (no starvation and at a prey density of 16 individuals mL−−1). The effect of starvation time on the numerical response was evident only at the higher prey density.  相似文献   

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