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1.
This paper demonstrates how discrete-time models describing population dynamics of two competing species can be derived in a bottom-up manner by considering competition for resources among individuals and the spatial distribution of individuals. The competition type of each species is assumed to be either scramble, contest, or an intermediate between them. Individuals of two species are distributed over resource sites or patches following one of three distribution functions. According to the combination of competition types of the two species and the distribution of individuals, various interspecific competition models are derived. Furthermore, a general interspecific competition model that includes various competition models as special cases is derived for each distribution of individuals. Finally, this paper examines dynamics of some of the derived competition models and shows that the likelihood of coexistence of the two species varies greatly, depending on the type of spatial distribution of individuals.  相似文献   

2.
For insects exploiting spatially structured arrays of resource patches (host plants, fungi, carrion, etc.), the distribution of individuals among patches can have important consequences for the coexistence of competitors. In general, intraspecific aggregation of consumer individuals over the landscape of patches stabilizes competition. Oviposition behavior of individual females can generate aggregation of larvae across patches and, therefore, strongly influences the outcome of competition between co-occurring species. We used simulation models to evaluate the consequences (for the coexistence of competitors) of different movement behaviors by females before and between oviposition events. Coexistence times increase when females are more likely to travel among neighboring patches than among distant ones. Coexistence times are also longer when females begin egg laying near the site of their emergence. Preoviposition dispersal is, therefore, destabilizing. We also considered responses by females to edges of resource arrays. Edge effects are generally stabilizing, delaying competitive exclusion by increasing larval aggregation, but different responses to edges have dramatically different effects on coexistence. The longest coexistence times occur when edges are "sticky", such that females encountering an edge tend to remain there.  相似文献   

3.
1. Intraspecific aggregation at a single spatial scale can promote the coexistence of competitors. This paper demonstrates how this same mechanism can be applied to the many systems that are patchy at two scales, with patches nested within 'superpatches'.
2. Data are presented from a field study showing that insects living in rotting fruits have aggregated distributions in the fruits under a single tree, and that the mean density and degree of aggregation varies significantly among trees. Observations in this system motivate the following models.
3. A model of competition has been developed between two species which explicitly represents spatial variation at two scales. By integrating the probability distributions for each scale, the marginal distributions of competitors over all patches can be found and used to calculate coexistence criteria. This model assumes global movement of the competitors.
4. Although spatial variation at a single scale may not be sufficient for coexistence, the total variation over all patches can allow coexistence. Variation in mean densities among superpatches and variation in the degree of aggregation among superpatches both promote coexistence, but act in different ways.
5. A second model of competition between two species is described which incorporates the effects of limited movement among superpatches. Limited movement among superpatches generally promotes coexistence, and also leads to correlations among aggregation and the mean densities of competitors.  相似文献   

4.
This paper provides first-principles derivations of population models for competition involving multiple resources with different competition types, based on resource partitioning between individuals. The following two cases are investigated. The first is the case in which the resource competed for and its competition type change depending on life stages from scramble to contest competition, or from contest to scramble competition. The second is the case in which individuals compete for two resources simultaneously with scramble and contest types, respectively. In both cases, population models are derived analytically, and in particular, the Hassell model is derived in the second case. The nature of reproduction curves and the stability properties of three population models derived are compared with each other. These models provide three representative models for competition involving both scramble and contest types.  相似文献   

5.
6.
The purpose of this paper is to present a unified view to understand mechanistic basis of various discrete-time population models from the viewpoints of resource partitioning and spatial aggregation of individuals. A first-principles derivation is presented of a new population model which incorporates both scramble and contest competition using a site-based framework in which individuals are distributed over discrete resource sites. The derived model has parameters relating to the way of resource partitioning and the degree of spatial aggregation of individuals, respectively. The model becomes various population models in various limits in these parameters. This model thus provides a unified view to understand how various population models are interrelated. The dependence of the stability of the model on the parameters is also examined.  相似文献   

7.
The model of N. D. Atkinson and B. Shorrocks (J. Anim. Ecol. 50, 461–471 (1981)) as two competing species distributing their progeny amongst patches according to independent negative binomial distributions. The resulting separation of the species increases the likelihood of coexistence. We have assumed a much simpler distribution of the competitors which has enabled us to explore analytically the dynamics of interactions with two competing species and a shared natural enemy in a patchy environment. Two types of natural enemy have been considered: a generalist predator whose dynamics are uncoupled from those of the two prey species, and a specialist (e.g., a parasitoid) whose dynamics are entirely coupled to those of its two prey. The following conclusions emerge. Non-aggregating generalist predators causing random predation across patches are generally destabilizing (although asymmetrical predation may in some case enhance coexistence as a result of preferential predation on the superior competitor). Predator aggregation in patches of high prey density, however, produces a switching effect which tends to promote stability. Coexistence is now even possible with high degrees of correlation in the distribution of the two prey and in situations of extreme competition where the competition coefficients exceed one. The main difference in the models with a specialist parasitoid as the natural enemy is a reduction in stability compared with the equivalent generalist-prey interaction. But stable coexistence can still readily occur if the natural enemies aggregate markedly in patches of high prey density.  相似文献   

8.
We give necessary and sufficient conditions for stochastically bounded coexistence in a class of models for two species competing in a randomly varying environment. Coexistence is implied by mutual invasibility, as conjectured by Turelli. In the absence of invasibility, a species converges to extinction with large probability if its initial population is small, and extinction of one species must occur with probability one regardless of the initial population sizes. These results are applied to a general symmetric competition model to find conditions under which environmental fluctuations imply coexistence or competitive exclusion.  相似文献   

9.
Understanding species coexistence has long been a major goal of ecology. Coexistence theory for two competing species posits that intraspecific density dependence should be stronger than interspecific density dependence. Great tits and blue tits are two bird species that compete for food resources and nesting cavities. On the basis of long‐term monitoring of these two competing species at sites across Europe, combining observational and manipulative approaches, we show that the strength of density regulation is similar for both species, and that individuals have contrasting abilities to compete depending on their age. For great tits, density regulation is driven mainly by intraspecific competition. In contrast, for blue tits, interspecific competition contributes as much as intraspecific competition, consistent with asymmetric competition between the two species. In addition, including age‐specific effects of intra‐ and interspecific competition in density‐dependence models improves predictions of fluctuations in population size by up to three times.  相似文献   

10.
Aggregation during dispersal can allow persistence of weak competitors, by creating conditions where stronger competitors are more likely to interact with conspecifics than with heterospecifics. However, aggregation mechanisms operate over a wide range of spatial scales, and species experience space in very different ways. The net effect of dispersal aggregation on coexistence will depend on how these scales interact. We show that it is possible to approximate the effects of aggregated dispersal on coexistence by considering three empirically measurable parameters: the spatial scale of interaction (how strongly competition drops off with distance), the spatial scale of aggregation (how large propagule packets are), and the temporal scale of aggregation (how frequently packets arrive). We use a novel metacommunity moment closure based on this approximation and stochastic simulations to show that aggregated dispersal allows for coexistence only when the stronger competitor is both aggregated and interacts at the same or a smaller spatial scale than the weaker competitor. When species interact and are aggregated at the same scales, coexistence outcomes are only weakly sensitive to the absolute scales of interaction and aggregation, as long as the scale of interaction is smaller than the scale of aggregation. However, coexistence is sensitive to the time‐scale of aggregation: increasing the frequency of packet arrival substantially reduces the region of fitness inequalities where both species persist. Finally, coexistence is less likely and global extinction of both competitors is more frequent when aggregation is fixed (with a constant number of propagules per packet), compared to density‐dependent (number of propagules increases with adult density).  相似文献   

11.
Coexistence of apparently similar species remains an enduring paradox in ecology. Spatial structure has been predicted to enable coexistence even when population-level models predict competitive exclusion if it causes each species to limit its own population more than that of its competitor. Nevertheless, existing hypotheses conflict with regard to whether clustering favours or precludes coexistence. The spatial segregation hypothesis predicts that in clustered populations the frequency of intra-specific interactions will be increased, causing each species to be self-limiting. Alternatively, individuals of the same species might compete over greater distances, known as heteromyopia, breaking down clusters and opening space for a second species to invade. In this study we create an individual-based model in homogeneous two-dimensional space for two putative sessile species differing only in their demographic rates and the range and strength of their competitive interactions. We fully characterise the parameter space within which coexistence occurs beyond population-level predictions, thereby revealing a region of coexistence generated by a previously-unrecognised process which we term the triadic mechanism. Here coexistence occurs due to the ability of a second generation of offspring of the rarer species to escape competition from their ancestors. We diagnose the conditions under which each of three spatial coexistence mechanisms operates and their characteristic spatial signatures. Deriving insights from a novel metric — ecological pressure — we demonstrate that coexistence is not solely determined by features of the numerically-dominant species. This results in a common framework for predicting, given any pair of species and knowledge of the relevant parameters, whether they will coexist, the mechanism by which they will do so, and the resultant spatial pattern of the community. Spatial coexistence arises from complementary combinations of traits in each species rather than solely through self-limitation.  相似文献   

12.
Coexistence of macroparasites is studied by extending the infinite-dimensional model considered by Anderson and May (1978, J. Anim. Ecol. 47, 219-247, 249-267) to several species of parasites that are assumed to interact only by causing the death of a common host. An exact invadability condition is found for this model. By studying when mutual invasibility is possible, the region where two parasite species can coexist is found. The result is that, if there is a trade-off between virulence and transmissibility, then coexistence of two species of parasites is possible, but only when the parameters of the model fall into a very narrow parameter region. If, on the other hand, one parasite is more virulent and less transmissible, then it will be competitively excluded. This latter result, though expected in terms of competition theory, is in contrast with what found in the approximate models so far used for studying interacting macroparasites. The effect of parasite aggregation on coexistence is studied by considering two modifications of the basic model (clumped infections and host population heterogeneity in predisposition to infections) that allow for higher aggregation. It appears that the width of the coexistence region is insensitive to these modifications.  相似文献   

13.
In sessile organisms such as plants, interactions occur locally so that important ecological aspects like frequency dependence are manifest within local neighborhoods. Using probabilistic cellular automata models, we investigated how local frequency-dependent competition influenced whether two species could coexist. Individuals of the two species were randomly placed on a grid and allowed to interact according to local frequency-dependent rules. For four different frequency-dependent scenarios, the results indicated that over a broad parameter range the two species could coexist. Comparisons between explicit spatial simulations and the mean-field approximation indicate that coexistence occurs over a broader region in the explicit spatial simulation.  相似文献   

14.
Inouye BD 《Oecologia》2005,145(2):188-196
Species that live in patchy and ephemeral habitats can compete strongly for resources within patches at a small scale. The ramifications of these interactions for population dynamics and coexistence at regional scales will depend on the intraspecific and interspecific distributions of individuals among patches. Spatial heterogeneity due to independent aggregation of competitors among patchy habitats is an important mechanism maintaining species diversity. I describe regional patterns of aggregation for four species of insect larvae in the fruits of Apeiba membranacea, a Neotropical rainforest tree. This aggregation results from variation in densities at a small scale (among the fruits under a single tree), compounded by significant variation among trees in both mean densities and degrees of aggregation. Both the degrees of aggregation and mean densities are statistically independent within and across species at both spatial scales. I evaluate the regional consequences of these spatial patterns by using maximum likelihood methods to parameterize a model that includes both explicit measures of the strength of competition and spatial variation at both within- and among-tree spatial scales. Despite strong competitive interactions among these species, during 2 years the observed spatial variation at both scales combined was sufficient to explain the coexistence of these species, although other coexistence mechanisms may also operate simultaneously. The observed spatial variation at small spatial scales may not be sufficient for coexistence, indicating the importance of considering multiple sources of spatial heterogeneity when scaling up from experiments that investigate local interactions to regional patterns of coexistence.  相似文献   

15.
Competitive interactions and invasibility between short- and long-distance dispersal was investigated in a population on a heterogeneous landscape with spatial correlations in habitat types, and where the driving interaction between individuals is competition for space. Stochastic spatially explicit simulations were used, along with differential equation models based on pair approximations. Conditions under which either dispersal strategy can successfully invade the other were determined, as a function of the amount and clustering of suitable habitat and the relative costs involved in the two dispersal strategies. Long-distance dispersal, which reduces intraspecific competition, is sometimes advantageous even where aggregation of suitable habitat would otherwise favor short-distance dispersal, although certain habitat distributions can lead to either strategy being dominant. Coexistence is also possible on some landscapes, where the spatial structure of the populations partitions suitable sites according to the number of suitable neighboring sites. Mutual competitive exclusion, where whichever strategy is established first cannot be invaded, is also possible. All of these results are observed even when there is no intrinsic difference in the two strategies' costs, such as mortality or competitive abilities.  相似文献   

16.
The two-species population dynamics model is the simplest paradigm of inter- and intra-species interaction. Here, we present a generalized Lotka–Volterra model with intraspecific competition, which retrieves as particular cases, some well-known models. The generalization parameter is related to the species habitat dimensionality and their interaction range. Contrary to standard models, the species coupling parameters are general, not restricted to non-negative values. Therefore, they may represent different ecological regimes, which are derived from the asymptotic solution stability analysis and are represented in a phase diagram. In this diagram, we have identified a forbidden region in the mutualism regime, and a survival/extinction transition with dependence on initial conditions for the competition regime. Also, we shed light on two types of predation and competition: weak, if there are species coexistence, or strong, if at least one species is extinguished.  相似文献   

17.
Chen B  Kang L 《Oecologia》2005,144(2):187-195
Species that live in patchy and ephemeral habitats can compete strongly for resources within patches at a small scale. The ramifications of these interactions for population dynamics and coexistence at regional scales will depend on the intraspecific and interspecific distributions of individuals among patches. Spatial heterogeneity due to independent aggregation of competitors among patchy habitats is an important mechanism maintaining species diversity. I describe regional patterns of aggregation for four species of insect larvae in the fruits of Apeiba membranacea, a Neotropical rainforest tree. This aggregation results from variation in densities at a small scale (among the fruits under a single tree), compounded by significant variation among trees in both mean densities and degrees of aggregation. Both the degrees of aggregation and mean densities are statistically independent within and across species at both spatial scales. I evaluate the regional consequences of these spatial patterns by using maximum likelihood methods to parameterize a model that includes both explicit measures of the strength of competition and spatial variation at both within- and among-tree spatial scales. Despite strong competitive interactions among these species, during 2 years the observed spatial variation at both scales combined was sufficient to explain the coexistence of these species, although other coexistence mechanisms may also operate simultaneously. The observed spatial variation at small spatial scales may not be sufficient for coexistence, indicating the importance of considering multiple sources of spatial heterogeneity when scaling up from experiments that investigate local interactions to regional patterns of coexistence.  相似文献   

18.
Heteromyopia and the spatial coexistence of similar competitors   总被引:7,自引:2,他引:5  
Most spatial models of competing species assume symmetries in the spatial scales of dispersal and interactions. This makes analysis tractable, and has led to the conclusion that segregation of species in space does not promote coexistence. However, these symmetries leave parts of the parameter space uninvestigated. Using a moment‐approximation method, we present a spatial version of the Lotka–Volterra competition equations to investigate effects of removing symmetries in the distances over which individuals disperse and interact. Some spatial segregation of the species always comes about due to competition, and such segregation does not necessarily lead to coexistence. But, if interspecific competition occurs over shorter distances than intraspecific competition (heteromyopia), spatial segregation becomes strong enough to promote coexistence. Such coexistence is most likely when the species have similar dynamics, in contrast to the competition–colonization trade‐off that requires large competitive differences between species.  相似文献   

19.
We investigated a mathematical model of the dynamics of the ecological system consisting of two competing perennial species, each of which leads a sedentary life. It is an individual-based model, in which the growth of each individual is described. The rate of this growth is weakened by competition from neighboring individuals. The strength of the competitors' influence depends on their size and distance to them. The conditions, in which the competitive exclusion of one of the competitors and the coexistence of both competitors take place are provided. The influence of the parameters responsible for the strength of competition, the degree of competitive asymmetry, and consideration of the importance of specific elements of the spatial structure of this ecological system on the results of the competition were analyzed. Both species co-exist when they are equal competitors. Permanent coexistence is possible only when interspecific competition is weaker than intraspecific. When interspecific competition is stronger, the coexistence of equal interspecific competitors is random. Both species have equal probability of extinction. If species are not equal competitors, the stronger one wins. This result can be modified by different strengths of intraspecific competition. The weaker interspecific competitor can permanently coexist with stronger one, when its individuals suffer stronger intraspecific competition.  相似文献   

20.
Spatial coexistence depends on a variety of biological and physical processes, and the relative scales of these processes may promote or suppress coexistence. We model plant competition in a spatially varying environment to show how shifting scales of dispersal, competition, and environmental heterogeneity affect coexistence. Spatial coexistence mechanisms are partitioned into three types: the storage effect, nonlinear competitive variance, and growth-density covariance. We first describe how the strength of each of these mechanisms depends on covariances between population densities and between population densities and the environment, and we then explain how changes in the scales of dispersal, competition, and environmental heterogeneity should affect these covariances. Our quantitative approach allows us to show how changes in the scales of biological and physical processes can shift the relative importance of different classes of spatial coexistence mechanisms and gives us a more complete understanding of how environmental heterogeneity can enable coexistence. For example, we show how environmental heterogeneity can promote coexistence even when competing species have identical responses to the environment.  相似文献   

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