Classical and resource-based competition: a unifying graphical approach

A graphical technique is given for determining the outcome of two species competition for two resources. This method is unifying in the sense that the graphical criterion leading to the various outcomes of competition are consistent across most of the spectrum of resource types (from those that fulfill the same growth needs to those that fulfill different needs) regardless of the classification method used, and the resulting graphs bear a striking resemblance to the well-known phase portraits for two species Lotka–Volterra competition. Our graphical method complements that of Tilman. Both include zero net growth isoclines. However, instead of using the consumption vectors at potential coexistence equilibria to determine input resource concentrations leading to specific competitive outcomes, we introduce curves bounding the feasible set (the set where the resource concentrations of any equilibrium solution must be located). The washout equilibrium (corresponding to the supply point) occurs at an intersection of curves defining the feasible set boundary. The resource concentrations of all other equilibria are found where zero net growth isoclines either intersect each other inside the feasible set or they intersect the feasible set boundary. A species has positive biomass at such an equilibrium only if its zero net growth isocline is involved in such an intersection. The competitive outcomes are then determined from the position of the single species equilibria, just as in the phase portrait analysis for classical competition (rather than from information at potential coexistence equilibria as in Tilman’s method).     

Plant interspecies competition for sunlight: a mathematical model of canopy partitioning

We examine the influence of canopy partitioning on the outcome of competition between two plant species that interact only by mutually shading each other. This analysis is based on a Kolmogorov-type canopy partitioning model for plant species with clonal growth form and fixed vertical leaf profiles (Vance and Nevai in J. Theor. Biol., 2007, to appear). We show that canopy partitioning is necessary for the stable coexistence of the two competing plant species. We also use implicit methods to show that, under certain conditions, the species’ nullclines can intersect at most once. We use nullcline endpoint analysis to show that when the nullclines do intersect, and in such a way that they cross, then the resulting equilibrium point is always stable. We also construct surfaces that divide parameter space into regions within which the various outcomes of competition occur, and then study parameter dependence in the locations of these surfaces. The analysis presented here and in a companion paper (Nevai and Vance, The role of leaf height in plant competition for sunlight: analysis of a canopy partitioning model, in review) together shows that canopy partitioning is both necessary and, under appropriate parameter values, sufficient for the stable coexistence of two hypothetical plant species whose structure and growth are described by our model. A. L. Nevai was supported in part by the National Institutes of Health, National Research Service Award (T32-GM008185) from the National Institute of General Medical Sciences (NIGMS).     

Coexistence of two competitors on one resource and one inhibitor: a chemostat model based on bacteria and antibiotics

We present a continuous time model of the dynamics of two species competing for a single limiting resource in the presence of a substance that inhibits the growth of one of the species. Resource and inhibitor are both derived from external sources. These inputs, and all other model parameters, are assumed to be constant in space and time. There exist conditions that permit the stable coexistence of the competitors, provided that the sensitive species is more efficient in exploiting the limiting resource, and the resistant species removes the inhibitor from the environment. There exists a subset of these conditions wherein the sensitive species can become established if and only if the resistant species is already established. If the resistant species does not remove the inhibitor from the environment, then coexistence of sensitive and resistant species is structurally unstable. If the resistant species produces the inhibitor, then coexistence is dynamically unstable. We review several studies of bacterial competition in the presence of antibiotics that support these conclusions.     

物种对资源竞争的动力机制及数值模拟

建立了集合种群物种在两个斑块中对资源竞争的数学模型,并进行了数值模拟实验,结果表明：（1）通过R^＊来预测竞争物种的结局,存在几种可能性：一是具有低R^＊值的物种竞争取代高R^＊值的物种;二是具有不同R^＊值的物种,甚至是具有相同R^＊值的物种也存在共存的可能性;三是具有高R^＊值的物种也可以竞争排斥低R^＊值的物种,结论存在不确定性。（2）竞争物种的随机迁移形成了源一汇结构,对物种竞争共存具有促进作用,但弱的资源利用者（较高的R^＊）的迁移率不宜过高。（3）在种群统计率相同的条件下,资源增长率差异越大,越不利于消费者物种的共存;若种群统计率不相同,在资源增长率相同的情况下,物种共存又是不可能的,在自然界中,物种共存需要资源增长率的差异。（4）不同类型的资源增长对竞争物种的稳定性的影响是不同的。     

Coexistence of competitors in metacommunities due to spatial variation in resource growth rates; does R * predict the outcome of competition?

Simple mathematical models are used to investigate the coexistence of two consumers using a single limiting resource that is distributed over distinct patches, and that has unequal growth rates in the different patches. Relatively low movement rates or high demographic rates of an inefficient resource exploiter allow it to coexist at a stable equilibrium with a more efficient species whose ratio of movement to demographic rates is lower. The range of conditions allowing coexistence depends on the between‐patch heterogeneity in resource growth rates, but this range can be quite broad. The between‐patch movement of the more efficient consumer turns patches with high resource growth rates into sources, while low‐growth‐rate patches effectively become sinks. A less efficient species can coexist with or even exclude the more efficient species from the global environment if it is better able to bias its spatial distribution towards the source patches. This can be accomplished with density independent dispersal if the less efficient species has a lower ratio of per capita between‐patch movement rate to demographic rates. Conditions that maximize the range of efficiencies allowing coexistence of two species are: a relatively high level of heterogeneity in resource growth conditions; high dispersal (or low demographic rates) of the superior competitor; and low dispersal (or high demographic rates) of the inferior competitor. Global exclusion of the more efficient competitor requires that the inferior competitor have sufficient movement to also produce a source‐sink environment.     

Hutchinson revisited: Patterns of density regulation and the coexistence of strong competitors

Ecologists have long been searching for mechanisms of species coexistence, particularly since G.E. Hutchinson raised the ‘paradox of the plankton’. A promising approach to solve this paradox and to explain the coexistence of many species with strong niche overlap is to consider over-compensatory density regulation with its ability to generate endogenous population fluctuations.Previous work has analysed the role of over-compensation in coexistence based on analytical approaches. Using a spatially explicit time-discrete simulation model, we systematically explore the dynamics and conditions for coexistence of two species. We go beyond the analytically accessible range of models by studying the whole range of density regulation from under- to very strong over-compensation and consider the impact of spatial structure and temporal disturbances. In particular, we investigate how coexistence can emerge in different types of population growth models.We show that two strong competitors are able to coexist if at least one species exhibits over-compensation. Analysing the time series of population dynamics reveals how the differential responses to density fluctuations of the two competitors lead to coexistence: The over-compensator generates density fluctuations but is the inferior competitor at strong amplitudes of those fluctuations; the competitor, therefore, becomes frequent and dampens the over-compensator's amplitudes, but it becomes inferior under dampened fluctuations.These species interactions cause a dynamic alternation of community states with long-term persistence of both species. We show that a variety of population growth models is able to reproduce this coexistence although the particular parameter ranges differ among the models. Spatial structure influences the probability of coexistence but coexistence is maintained for a broad range of dispersal parameters.The flexibility and robustness of coexistence through over-compensation emphasize the importance of nonlinear density dependence for species interactions, and they also highlight the potential of applying more flexible models than the classical Lotka-Volterra equations in community ecology.     

同域分布大熊猫和水鹿生境利用分异特征

野生动物的生境利用特征研究是动物生态学核心问题之一,同域分布动物对生境的利用特征及共存机制是其重要组成部分,也是实现珍稀濒危物种保护与栖息地恢复的基础。基于空间利用和生境因子选择差异研究了卧龙自然保护区同域分布大熊猫(Ailuropoda melanoleuca)和水鹿(Rusa unicolor)的生境利用关系,探讨了同域分布野生动物在生境因子选择和空间利用的分异特征。结果表明:(1)空间利用上,大熊猫和水鹿的空间重叠系数为58.35%,其中,在原始林和次生林生境中的空间重叠系数分别为66.58%和36.64%,二者在原始林中的空间重叠较高;(2)生境因子选择上,大熊猫和水鹿对物理因子的选择有坡位、离小路距离和离水源距离3个变量有显著性差异,对生物因子的选择有乔木密度、灌木盖度、灌木密度、竹林盖度、幼竹密度、幼竹基径、幼竹高度、成竹高度和死竹密度9种变量有显著性差异;(3)大熊猫和水鹿都表现为更偏好原始林生境,但大熊猫对原始林的依赖性更强。分析同域分布动物的生境利用关系有利于深入了解不同动物对资源的空间利用特征及共存机制,可以为保护区制定珍稀野生动物保护和栖息地恢复政策提供科学依据。     

The impact of consumer-resource cycles on the coexistence of competing consumers

This article seeks to determine the extent to which endogenous consumer-resource cycles can contribute to the coexistence of competing consumer species. It begins with a numerical analysis of a simple model proposed by Armstrong and McGehee. This model has a single resource and two consumers, one with a linear functional response and one with a saturating response. Coexistence of the two consumer species can occur when the species with a saturating response generates population cycles of the resource, and also has a lower resource requirement for zero population growth. Coexistence can be achieved over a wide range of relative efficiencies of the two consumers provided that the functional response of the saturating consumer reaches its half-saturation value when the resource population is a small fraction of its carrying capacity. In this case, the range of efficiencies allowing coexistence is comparable to that when two competitors have stable dynamics and a high degree of resource partitioning. A variety of modifications of this basic model are analyzed to investigate the consequences for coexistence of different resource growth equations, different functional and numerical response shapes, and other factors. Large differences in functional response shape appear to be the most important factor in producing robust coexistence via resource cycles. If the unstable species has a concave numerical response, this greatly expands the conditions allowing coexistence. If the stable consumer species has a convex (accelerating) functional and/or numerical response, the range of conditions allowing coexistence is also expanded. We argue that large between-species differences in functional response form can often be produced by between-consumer differences in the adaptive adjustments of foraging effort to food density. Consumer-resource cycles can also expand the conditions allowing coexistence when there is resource partitioning, but do so primarily when resource partitioning is relatively slight; this makes the ease of coexistence relatively independent of consumer similarity.     

Resource partitioning among competing species—A coevolutionary approach

A reasonably general theory for predicting the outcome of coevolution among interacting species is developed. It is applied to a model for resource partitioning among competing species.Current theory for resource partitioning is based on derivations of a “limiting similarity”—i.e., a limit to how similar competitors can be to one another consistent with coexistence. This theory presumes there is a mechanism, perhaps invasion and extinction, which causes competitors to attain the limiting similarity. The view taken in this paper is that partitioning is an evolutionary compromise between pressures for character displacement and disadvantages inherent in the shift to different resource types.A set of principles is offered for the evolution of the parameters in ecological models. (1) For single population models natural selection causes the parameters ultimately to assume those values which produce the highest equilibrium population size. (2) For models of interacting populations, but without interspecific frequency-dependence, natural selection causes the parameters to assume values which produce either the highest or lowest equilibrium population size for any species depending on the sign of the “feedback” in the community obtained by deleting that species. (3) For models of interacting populations with interspecific frequency dependence natural selection leads to parameter values which produce intermediate equilibrium population sizes. A function called the conditional equilibrium population size is introduced. Provided (a) the mean fitness is a maximum in each species at a stable coevolutionary equilibrium and (b) there is negative density-dependence in each species then natural selection causes the parameters to assume values which produce the highest conditional equilibrium population size for each species.These coevolutionary principles, applied to a model for resource partitioning, entail that the niche separation between species relative to given niche widths, increases with the variety of available resources and decreases with the number of competing populations. Also, the evolution of character displacement between two species does not proceed far enough to maximize the equilibrium population sizes of the species involved. These results imply that the relationship between the niche overlap (of nearest neighbors) and species diversity is qualitatively different depending on whether the variety of resources at any place covaries with the species diversity there. Without covariation niche overlap increases with species diversity; with covariation overlap may decrease with species diversity. This study provides the beginning of a theory for the convergent evolution of community structure.     

Niche modification and stability of competitive systems. II. Persistence of interspecific competitive systems with parasitoid wasps

Effects of niche shift in ecological time scale on the population dynamics of competing species were studied in the experimental populations of two parasitoid wasp species, Anisopteromalus calandrae and Heterospilus prosopidis (both are solitary parasites), on a host, the azuki bean weevil, Callosobruchus chinensis. Four resource conditions were set up with combination of kind of bean (azuki or black eye), and host distribution (uniform or clumped). In each resource condition, four developmental stages of hosts were provided as a resource spectrum for parasitoid wasps. Population dynamics of the two wasp populations were investigated in each resource condition in Multi-Generation Competitive Systems (MGCS), in which fresh hosts of four developmental stages were periodically introduced and were parasitized competitively by the two wasp species. Competitive coexistence of both wasps occurred in the azuki-clumped condition, where the peaks of the resource utilization curves separated in the two species; pupae in A. calandrae and the early or late fourth instar in H. prosopidis, A. calandrae was eliminated in the azuki-uniform condition and H. prosopidis went extinct in two black eye conditions irrespective of host distributions. The degrees of overlap of the resource utilization patterns of the two wasp species during population dynamics were not significantly different among resource conditions irrespective of the results of coexistence or extinction. Even in the azuki-clumped condition, however, extinction of A. calandrae was observed when resource partitioning could not be realized with only the late fourth instar larvae available to wasps. Further analytical experiments showed that parasitizing ability of A. calandrae increased with host density per bean with azuki beans, but A. calandrae could express higher parasitizing ability with black eye beans than H. prosopidis irrespective of host density per bean. The flexibility in parasitizing ability by A. calandrae for various host stages under different resource conditions was thought to be the major factor in determining the competitive coexistence or the extinction of either species under different resource conditions. The present experiments also suggested that different second-best host stages between competitors could be a major contributing factor to competitive coexistence.     

Compartmentalization and niche differentiation: causal patterns of competition and coexistence

The current major models of coexistence of species on the same resources are briefly summarized. It is then shown that analysis of supposedly competitive systems in terms of the physical four dimensions of phase-space is sufficient to understand the causes for coexistence and for competitive exclusion. Thus, the multiple dimensions of niche theory are reduced to factors which define the magnitudes of the phase-spatial system, in particular the boundaries of population spaces and of periods of activity. Excluding possible cooperative interaction between consumers, it appears that coexistence of species on thesame kind of limiting resource is possible only in cases of compartmentalization either in space, or in time, of resource consumption, i.e. if each consumer species disposes of a separate resource supply. Three criteria were found to be decisive for successful compartmentalization (i.e. for coexistence): 1. the vector of the resource flow; 2. relative mobility between consumers and resource units; 3. dependence or independence of resource flow on previous consumption. The traditional terminology of niche theory and of competition theory in general proved to be inadequate for analytical treatment of problems of coexistence.     

Coexistence of cycling and dispersing consumer species: Armstrong and McGehee in space

Two competing consumer species may coexist using a single homogeneous resource when the more efficient consumer--the one having the lowest equilibrium resource density--has a more nonlinear functional response that generates consumer-resource cycles. We extend this model of nonequilibrium coexistence, as proposed by Armstrong and McGehee, by putting the interaction into a spatial context using two frameworks: a spatially explicit individual-based model and a spatially implicit metapopulation model. We find that Armstrong and McGehee's mechanism of coexistence can operate in a spatial context. However, individual-based simulations suggest that decreased dispersal restricts coexistence in most cases, whereas differential equation models of metapopulations suggest that a low rate of dispersal between subpopulations often increases the coexistence region. This difference arises in part because of two potentially opposing effects on coexistence due to the asynchrony in the temporal dynamics at different locations. Asynchrony implies that the less efficient species is more likely to be favored in some spatial locations at any given time, which broadens the conditions for coexistence. On the other hand, asynchrony and dispersal can also reduce the amplitude of local population cycles, which restricts coexistence. The relative influence of these two effects depends on details of the population dynamics and the representation of space. Our results also demonstrate that coexistence via the Armstrong-McGehee mechanism can occur even when there is little variation in the global densities of either the consumers or the resource, suggesting that empirical studies of the mechanisms should measure densities on several spatial scales.     

A new hypothesis for species coexistence: male–male repulsion promotes coexistence of competing species

We propose a new hypothesis for species coexistence by considering behavioral interactions between individuals. The hypothesis states that repulsive behavior between conspecific males (male–male repulsion) creates space for competing species, which promotes their coexistence. This hypothesis can explain the coexistence of two competing species even when their ecological niches completely overlap in spatially homogeneous environments. In addition, the mechanisms underlying such behavior might play a role in enabling the coexistence of two species immediately after speciation, with little or no niche differentiation, as in the case of cichlid fish communities, for example. Although there is limited evidence supporting this hypothesis, it can nevertheless explain the occurrence of species coexistence and biodiversity, which cannot be explained by previous theories.     

Nitrogen preferences and plant-soil feedbacks as influenced by neighbors in the alpine tundra

Plant resource partitioning of chemical forms of nitrogen (N) may be an important factor promoting species coexistence in N-limited ecosystems. Since the microbial community regulates N-form transformations, plant partitioning of N may be related to plant–soil feedbacks. We conducted a ¹⁵N tracer addition experiment to study the ability of two alpine plant species, Acomastylis rossii and Deschampsia caespitosa, to partition organic and inorganic forms of N. The species are codominant and associated with strong plant–soil feedbacks that affect N cycling. We manipulated interspecific interactions by removing Acomastylis or Deschampsia from areas where the species were codominant to test if N uptake patterns varied in the presence of the other species. We found that Deschampsia acquired organic and inorganic N more rapidly than Acomastylis, regardless of neighbor treatment. Plant N uptake—specifically ammonium uptake—increased with plant density and the presence of an interspecific neighbor. Interestingly, this change in N uptake was not in the expected direction to reduce niche overlap and instead suggested facilitation of ammonium use. To test if N acquisition patterns were consistent with plant–soil feedbacks, we also compared microbial rhizosphere extracellular enzyme activity in patches dominated by one or the other species and in areas where they grew together. The presence of both species was generally associated with increased rhizosphere extracellular enzyme activity (five of ten enzymes) and a trend towards increased foliar N concentrations. Taken together, these results suggest that feedbacks through the microbial community, either in response to increased plant density or specific plant neighbors, could facilitate coexistence. However, coexistence is promoted via enhanced resource uptake rather than reduced niche overlap. The importance of resource partitioning to reduce the intensity of competitive interactions might vary across systems, particularly as a function of plant-soil feedbacks.     

Community robustness and limiting similarity in periodic environments

Temporal environmental variation has long been considered as one of the potential factors that could promote species coexistence. A question of particular interest is how the ecology of fluctuating environments relates to that of equilibrium systems. Equilibrium theory says that the more similar two species are in their modes of regulation, the less robust their coexistence will be; that is, the volume of external parameters for which all populations persist shrinks with increasing similarity. In this study, we will attempt to generalize these results to temporally varying situations and establish the precise mathematical relationship between the two. Our treatment considers unstructured populations in continuous time with periodic attractors of fixed period length, where the periodic behavior is due to external forcing. Within these conditions, our treatment is general. We provide a coherent theoretical framework for defining measures of species similarity and niche. Our main conclusion is that all factors that function to regulate population growth may be considered as separate regulating factors for each moment of time. In particular, a single resource becomes a resource continuum, along which species may segregate in the same manner as along classical resource continua. Therefore, we provide a mathematical underpinning for considering fluctuation-mediated coexistence as temporal niche segregation.     

Diets of sexual and sperm‐dependent asexual dace (Chrosomus spp.): relevance to niche differentiation and mate choice hypotheses for coexistence

Sperm‐dependent asexual species must coexist with a sexual species (i.e. a sperm source) to reproduce. The maintenance of this coexistence, and hence the persistence of sperm‐dependent asexual species, may depend on ecological niche separation or preference by males for conspecific (i.e. sexual) mates. We first modified an analytical model to consider both of these mechanisms acting simultaneously on the coexistence of the two species. Our model indicates that a small amount of niche separation between parental species and hybrids can facilitate coexistence by weakening the requirement for male mate preference. We also estimated niche separation empirically in the Chrosomus (formerly Phoxinus) sexual‐asexual system based on diet overlap between sperm‐dependent asexuals and their two sexual host species. Diet overlap between the sexual species was not significant in either lake, whereas the sperm‐dependent asexual had an intermediate niche that overlapped significantly, but somewhat asymmetrically, with both sexual species. These empirical results were then used to parameterize our analytical model to predict the minimum strength of male mate preference required to maintain coexistence in each lake. Some male mate preference is likely required to maintain coexistence in the Chrosomus system, but the minimum required preference depends on the severity of density dependence. Future empirical work on understanding coexistence in sperm‐dependent asexual systems would benefit from taking both niche separation and mate choice into account, and from simultaneous empirical estimates of male mate choice, niche separation, and density dependence.     

Coexistence in MacArthur-style consumer-resource models

The nature of and conditions for permanent coexistence of consumers and resources are characterized in a family of models that generalize MacArthur's consumer-resource model. The generalization is of the resource dynamics, which need not be of Lotka-Volterra form but are subject only to certain restrictions loose enough to admit many resource dynamics of biological interest. For any such model, (1) if there is an interior equilibrium, then it is globally attracting, else some boundary equilibrium is globally attracting-thus permanent coexistence is coexistence at a globally attracting equilibrium; (2) there is an interior equilibrium if and only if for any species, the equilibrium approached in the absence of that species and the presence of the others is invasible by that species--thus permanent coexistence is equivalent to mutual invasibility; (3) for resources without direct interactions, the conditions for permanent coexistence of the consumers admit an instructive formulation in terms of regression statistics. The significance and limitations of the models and results are discussed.     

Nonlinearity in interspecific interactions in response to climate change: Cod and haddock as an example

Climate change has profound ecological effects, yet our understanding of how trophic interactions among species are affected by climate change is still patchy. The sympatric Atlantic haddock and cod are co‐occurring across the North Atlantic. They compete for food at younger stages and thereafter the former is preyed by the latter. Climate change might affect the interaction and coexistence of these two species. Particularly, the increase in sea temperature (ST) has been shown to affect distribution, population growth and trophic interactions in marine systems. We used 33‐year long time series of haddock and cod abundances estimates from two data sources (acoustic and trawl survey) to analyse the dynamic effect of climate on the coexistence of these two sympatric species in the Arcto‐Boreal Barents Sea. Using a Bayesian state‐space threshold model, we demonstrated that long‐term climate variation, as expressed by changes of ST, affected species demography through different influences on density‐independent processes. The interaction between cod and haddock has shifted in the last two decades due to an increase in ST, altering the equilibrium abundances and the dynamics of the system. During warm years (ST over ca. 4°C), the increase in the cod abundance negatively affected haddock abundance while it did not during cold years. This change in interactions therefore changed the equilibrium population size with a higher population size during warm years. Our analyses show that long‐term climate change in the Arcto‐Boreal system can generate differences in the equilibrium conditions of species assemblages.     

Adaptive dynamics of competition for nutritionally complementary resources: character convergence, displacement, and parallelism

Consumers acquire essential nutrients by ingesting the tissues of resource species. When these tissues contain essential nutrients in a suboptimal ratio, consumers may benefit from ingesting a mixture of nutritionally complementary resource species. We investigate the joint ecological and evolutionary consequences of competition for complementary resources, using an adaptive dynamics model of two consumers and two resources that differ in their relative content of two essential nutrients. In the absence of competition, a nutritionally balanced diet rarely maximizes fitness because of the dynamic feedbacks between uptake rate and resource density, whereas in sympatry, nutritionally balanced diets maximize fitness because competing consumers with different nutritional requirements tend to equalize the relative abundances of the two resources. Adaptation from allopatric to sympatric fitness optima can generate character convergence, divergence, and parallel shifts, depending not on the degree of diet overlap but on the match between resource nutrient content and consumer nutrient requirements. Contrary to previous verbal arguments that suggest that character convergence leads to neutral stability, coadaptation of competing consumers always leads to stable coexistence. Furthermore, we show that incorporating costs of consuming or excreting excess nonlimiting nutrients selects for nutritionally balanced diets and so promotes character convergence. This article demonstrates that resource-use overlap has little bearing on coexistence when resources are nutritionally complementary, and it highlights the importance of using mathematical models to infer the stability of ecoevolutionary dynamics.     

Resource utilization by two insular endemic mammalian carnivores,the island fox and island spotted skunk

We compared resource utilization of two insular endemic mammalian carnivores, the island spotted skunk and island fox, along niche dimensions of space, food, and time on Santa Cruz Island. We predicted that resource use by foxes and skunks would differ along one or more niche dimensions, and that both species would have broader niches or higher densities compared with mainland relatives. Island foxes and island spotted skunks differed to some extent in habitat use, diets, and circadian activity, which may account for their long-term coexistence. Nonetheless, substantial overlap between skunks and foxes in spatial, dietary, and temporal dimensions suggests that competition between the two species does occur. Moreover, competition may be asymmetric, affecting skunks more than foxes. Compared with mainland foxes, island foxes have smaller body size, smaller home range, increased population density, increased diurnal activity, and behavior that is more highly inquisitive and less flightprone all common features of insular faunas. Island skunks, however, apparently have not developed these changes, perhaps due to asymmetric competition with foxes in conjunction with severe ecosystem disturbances caused by feral sheep.