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.     

Productivity, dispersal and the coexistence of intraguild predators and prey

A great deal is known about the influence of dispersal on species that interact via competition or predation, but very little is known about the influence of dispersal on species that interact via both competition and predation. Here, I investigate the influence of dispersal on the coexistence and abundance-productivity relationships of species that engage in intraguild predation (IGP: competing species that prey on each other). I report two key findings. First, dispersal enhances coexistence when a trade-off between resource competition and IGP is strong and/or when the Intraguild Prey has an overall advantage, and impedes coexistence when the trade-off is weak and/or when the Intraguild Predator has an overall advantage. Second, the Intraguild Prey's abundance-productivity relationship depends crucially on the dispersal rate of the Intraguild Predator, but the Intraguild Predator's abundance-productivity relationship is unaffected by its own dispersal rate or that of the Intraguild Prey. This difference arises because the two species engage in both a competitive interaction as well as an antagonistic (predator-prey) interaction. The Intraguild Prey, being the intermediate consumer, has to balance the conflicting demands of resource acquisition and predator avoidance, while the Intraguild Predator has to contend only with resource acquisition. Thus, the Intraguild Predator's abundance increases monotonically with resource productivity regardless of either species' dispersal rate, while the Intraguild Prey's abundance-productivity relationship can increase, decrease, or become hump-shaped with increasing productivity depending on the Intraguild Predator's dispersal rate. The important implication is that a species' trophic position determines the effectiveness of dispersal in sampling spatial environmental heterogeneity. The dispersal behavior of a top predator is likely to have a stronger effect on coexistence and spatial patterns of abundance than the dispersal behavior of an intermediate consumer.     

Life history and interspecies relationships of Chirocephalus diaphanus Prévost and Tanymastix stagnalis (L.), (Crustacea,Anostraca) inhabiting a group of mountain ponds in Latium,Italy

Life histories of two coexisting Anostracan species, inhabiting a group of mountain ponds in Latium (Pantani di Forca Canapine) are described and discussed, with particular regard to hatching requirements, growth rate, fecundity and life span.Unlike previously assumed (Mura, 1985), the cysts of the two species Tanymastix stagnalis and Chirocephalus diaphanus seem to respond to the same hatching stimuli, since their nauplii coexist and can be separated by morphological differences.Significant differences recorded as to size, time in attaining sexual maturity, fecundity and life span, are in favour of a niche separation by size and by time. In particular, size differences are supposed to reflect significant differences also at filtering apparatus level, thus allowing prey selection by size.     

Trade-offs between reproductive and somatic (storage) investments in animals: a comparative test of the Van Noordwijk and De Jong model

Classical life-history theory predicts ‘trade-offs’ between reproductive and somatic investments. However, empirical studies have shown that intraspecific phenotypic correlations between these two resource investments are often positive or nonsignificant, rather than negative as predicted. The model of Van Noordwijk and De Jong (1986) was proposed to explain these unexpected results. According to their model, positive correlations between reproductive and somatic investments will result if individual variation in resource acquisition exceeds that of resource allocation, whereas negative correlations will result if individual variation in resource allocation exceeds that of resource acquisition. To test this model, I used body storage/condition as an index of somatic investment because it is usually strongly related to level of resource acquisition. I predicted that laboratory studies should more often show negative correlations between reproductive and somatic investments than field studies, because individual variation in resource acquisition is expected to be lower in controlled laboratory environments than in variable natural environments. A literature review revealed that correlations between somatic (storage) investment and reproductive investment (estimated as clutch/litter mass, number of offspring per clutch/litter, or number of clutches/litters) among conspecific breeding female animals are more often positive (15 species) or nonsignificant (17 species) than negative (6 species). Moreover, as expected, five of six negative correlations were observed in laboratory studies, whereas 13 of 15 positive correlations were observed in field studies. It is concluded that future empirical and theoretical work on life histories should consider individual variation in both resource acquisition and allocation and the interaction between the two. This revised version was published online in July 2006 with corrections to the Cover Date.     

Spatial Heterogeneity in Habitat Quality and Cross-Scale Interactions in Metapopulations

Abstract Integration of habitat heterogeneity into spatially realistic metapopulation approaches reveals the potential for key cross-scale interactions. Broad-scale environmental gradients and land-use practices can create autocorrelation of habitat quality of suitable patches at intermediate spatial scales. Patch occupancy then depends not only on habitat quality at the patch scale but also on feedbacks from surrounding neighborhoods of autocorrelated patches. Metapopulation dynamics emerge from how demographic and dispersal processes interact with relevant habitat heterogeneity. We provide an empirical example from a metapopulation of round-tailed muskrats (Neofiber alleni) in which habitat quality of suitable patches was spatially autocorrelated most strongly within 1,000 m, which was within the expected dispersal range of the species. After controlling for factors typically considered in metapopulation studies—patch size, local patch quality, patch connectivity—we use a cross-variogram analysis to demonstrate that patch occupancy by muskrats was correlated with habitat quality across scales ≤1,171 m. We also discuss general consequences of spatial heterogeneity of habitat quality for metapopulations related to potential cross-scale interactions. We focus on spatially correlated extinctions and metapopulation persistence, hierarchical scaling of source–sink dynamics, and dispersal decisions by individuals in relation to information constraints.     

Landscape Ecotoxicology and Assessment of Risk at Multiple Scales

Traditional approaches to ecotoxicology and ecological risk assessment frequently have ignored the complexities arising due to the spatial heterogeneity of natural systems. In recent years, however, ecologists have become increasingly aware of the influence of spatial organization on ecological processes. Landscape ecology provides a conceptual and theoretical framework for the analysis of spatial patterns, the characterization of spatial aspects of ecosystem function, and the understanding of landscape dynamics. Incorporating the insights of landscape ecology into ecotoxicology will enhance our ability to understand and ultimately predict the effects of toxic substances in ecological systems. Ecological risk assessments need to explicitly consider multiple spatial scales, accounting for heterogeneity within contaminated areas and for the larger landscape context. A simple simulation model is presented to illustrate the effects of spatial heterogeneity by linking an individual-based toxicokinetic model with a spatially distributed metapopulation model. Dispersal of organisms between contaminated and uncontaminated patches creates a situation where risk analysis must consider a spatial extent broader than the toxicant-contaminated area. In general, the addition of a toxicant to a source patch (i.e., a net exporter of individuals) will have a greater impact than the same toxicant addition to a sink patch (i.e., a net importer of individuals).     

The Life Histories of Two Temporarily Coexisting,Pond Dwelling Cladocerans

Investigations on the life histories of two cladocerans, Moina brachiata and Daphnia obtusa, in a small, nearly temporary pond in South Germany revealed that M. brachiata is better adapted to fluctuating environmental conditions; the species dominated from May to October. D. obtusa was present in spring and autumn/winter but disappeared completely during the summer months. Both species coexisted for extended periods in spring and autumn; abundance of D. obtusa was generally by an order of magnitute lower. Four periods of low water level were slightly preceded by or coincided with a decrease of clutch size, a decrease of the proportion of egg bearing females indicating that both species suffered from food shortage. Laboratory investigations on life history parameters showed that the two species have different temperature tolerances and preferences. M. brachiata showed its highest reproductive success at 25 and 30°C but died at temperatures <15°C and ≥ 35°C. D. obtusa experienced a broader temperature range (2 to 25°C) but could not withstand temperatures ≥ 30°C. Short term starvation periods (3d) caused the death of M. brachiata females, while D. obtusa soon recovered and reproduced when being refed. M. brachiata is a typical r-species with early reproduction, rapid development, high population growth rates and a high tendency to produce resting eggs; D. obtusa pursues more the concept of k-selection.     

动物生活史进化理论研究进展

综述了生活史性状、生活史对策、权衡、适合度及进化种群统计学等动物生活史进化领域的进展。权衡是生活史性状之间相互联系的纽带,分为生理权衡与进化权衡。适合度是相对的,与个体所处的特定环境条件有关,性状进化与适合度之间关系紧密。适合度是生活史进化理论研究的焦点。探讨动物生活史对策的理论很多,影响最大的是MacArthur和Wilson提出的r对策及K对策理论。随年龄的增长,动物存活率及繁殖率逐步下降的过程,称为衰老;解释衰老的进化理论主要有突变-选择平衡假设和多效对抗假设。进化种群统计学将种群统计学应用于生活史进化研究,为探讨表型适合度的进化提供了有效的手段。将进化种群统计学、数量遗传学及特定种系效应理论进行整合,建立完整的动物生活史进化综合理论体系,是当代此领域的最大挑战。     

Life history theory and evolutionary anthropology

Life-history theory has been developed in biology to explain the variation in timing of fertility, growth, developmental rates, and death of living organisms, as well as events directly tied to these parameters. The theory is useful in explaining variations in age-specific human fertility and mortality patterns, as well as understanding how the human life course evolved to patterns so divergent from those that characterize our close primate relatives. Surprisingly, this same theory can also be used to explain why people often ignore the long-term consequences of behaviors that produce short-term gain.     

Life history strategies in two coexisting agamospecies of dandelion

Populations of Taraxacum , dandelion, on a Northumberland sand dune system contain 27 agamospecies. Demographic parameters for subpopulations containing a preponderance of two closely related agamospecies, Taraxacum lacistophyllum and T. brachyglossum are described. High and low density populations were stable over a 3 year period. The estimated turnover times differed between densities and species. The early growth characteristics of the two species are described. The plastochrons of the two species are distinct, as are the growth patterns of the leaves, the total leaf length per plant, the number of leaves and rate of leaf birth, and the patterns of allocation of dry weight to the root, shoot, and reproductive organs of the plant. Differences between the species were observed in fruit, scape height, the wind speed required to achieve fruit dispersal, and the pattern of fruit dispersal at different wind speeds. The origin and maintenance of agamospecies diversity is discussed in relation to the observed life history variation.     

Coexistence of competitive species with a stage-structured life cycle

Ecological theory provides explanations for exclusion or coexistence of competing species. Most theoretical works on competition dynamics that have shaped current perspectives on coexistence assume a simple life cycle. This simplification, however, may omit important realities. We present a simple two-stage structured competition model to investigate the effects of life-history characteristics on coexistence. The achievement and the stability of coexistence depend not only on competition coefficients but also on a set of life-history parameters that reflect the viability of an individual, namely, adult death rate, maturation rate, and birth rate. High individual viability is necessary for a species to persist, but it does not necessarily facilitate coexistence. Intense competition at the juvenile or adult stage may require higher or lower viability, respectively, for stable coexistence to be possible. The stability mechanism can be explained by the refuge effect of the less competitive stage, and the birth performance, which preserves the less competitive stage as a refuge. Coexistence might readily collapse if the life-history characteristics, which together constitute individual viability, change, even though two species have an inherent competitive relation conducive to stable coexistence.