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Decoys in Predation and Parasitism
Decoys in Predation and Parasitism

... some attempts to use them and bacteriophages for pathogen control (Westergaard and Kramer 1977; Smith and Huggins 1983; Jackson and Whiting 1992; Fratamico and Whiting 1995; Sarkar et al. 1996). Like bacteriophages, bacteria of the genus Bdellovibrio penetrate the outer envelope of their prey, take ...
Rapid Evolutionary Change and the Coexistence of Species
Rapid Evolutionary Change and the Coexistence of Species

... making coexistence more likely. In this framework a species’ mean fitness refers to the component of its population growth rate that is independent of its density and the density of competing species (see the sidebar on Ecological Versus Evolutionary Fitness for a further discussion of ecological fitn ...
Relationships Within Ecosystems
Relationships Within Ecosystems

... E. One organism benefits but the other does not benefit and is not harmed. F. parasitism ...
- ResearchOnline@JCU
- ResearchOnline@JCU

... were no longer evident in Australia, while they remained in the Bahamas, indicating that post-recruitment interactions may or may not obscure patterns established at recruitment. If the patterns we observed at recruitment were the result of consumption by predators, why would predators disproportion ...
A hierarchical model of whole assemblage island biogeography
A hierarchical model of whole assemblage island biogeography

... evolutionary biology. However, while many empirical studies suggest species differ in vital biogeographic rates, such as dispersal abilities, quantitative methods have had difficulty incorporating such differences into analyses of whole-assemblages. In particular, differences in dispersal abilities ...
Management strategies for plant invasions: manipulating
Management strategies for plant invasions: manipulating

... The predictions of the dynamic equilibrium model for the invasibility of different environments (Huston, 1994) are derived from its predictions for population survival and species diversity of plants in general, whether native or exotic, and address two distinct components of invasibility: (1) the p ...
Distribution/abundance relations in a New Zealand grassland
Distribution/abundance relations in a New Zealand grassland

... Abstract: There are many examples in the literature of a positive correlation between the distribution of a species and its local abundance, i.e., widely occurring species tend to be more abundant locally when they do occur. Such relations have been documented over a wide range of taxa and spatial s ...
Species-rich ecosystems are vulnerable to cascading extinctions in an increasingly variable world
Species-rich ecosystems are vulnerable to cascading extinctions in an increasingly variable world

... species-rich ecosystems than in species-poor ones due to increased intensity of competition—density compensation (reviewed by Gonzalez and Loreau 2009)—and lower densities should in turn lead to higher extinction risks. We also investigate how species richness and degree of correlation among species ...
The role of behavioural variation in the invasion of
The role of behavioural variation in the invasion of

Diversity effects on production in different light and fertility
Diversity effects on production in different light and fertility

... added total) in a replacement series design to account for differences in recruitment success between species of different seed sizes. The mass of seed added per plot per species was calculated by dividing seed mass (8 g) by the germination rate of the species (for monocultures), or by dividing the ...
Ecology - Defined - Academic Home Page
Ecology - Defined - Academic Home Page

... internal processes and functions ...
Accepted manuscript
Accepted manuscript

... correlation structure of ρ = 0, 0.5 or 1. This was incorporated into eqn. (1), communities were assembled following the same rules as above, checked for persistence, then initiated at equilibrium and simulated over 200 time-steps for different community sizes and values of rMAX and ρ. The CV(x) fro ...
Reiskind, M.H. and M.L. Wilson. 2008. Interspecific
Reiskind, M.H. and M.L. Wilson. 2008. Interspecific

... ABSTRACT Many invasive species succeed in becoming established in new locations because of their competitive superiority to native species. This has been shown in several examples involving mosquitoes. In this study, we examined the interspeciÞc competition between mosquito larvae of a well-establis ...
Fig. 3 - ePrints Soton - University of Southampton
Fig. 3 - ePrints Soton - University of Southampton

... www.nature.com/scientificreports/ and is further complicated by alterations in context, including resource availability48, habitat configuration7 and changing environmental conditions42,49,50. It follows therefore, that the mechanistic basis of species interactions are unlikely to be documented in ...
Population Ecology
Population Ecology

... individuals in a population per unit time. The term population growth can technically refer to any species, but almost always refers to humans, and it is often used informally for the more specific demographic term population growth rate. • All populations have the potential to grow exponentially wh ...
Environmental Fitness for Sustained Population Dynamics
Environmental Fitness for Sustained Population Dynamics

... in a different way. The conditions for agents survival and reproduction are set up locally, in both space and time. Agents evolve, and phenomena are observed on larger scales: periodic patterns (time), covering the whole environment (space). Ideally, the system could be designed by using preconditio ...
Sociality, densitydependence and microclimates determine the
Sociality, densitydependence and microclimates determine the

... at least six species of hibernating bats (Table S1) (Cryan et al. 2010). WNS is characterised by lesions on flight membranes of bats (Meteyer et al. 2009) which may disrupt patterns of torpor (Warnecke et al. 2012) or critical physiological processes and possibly result in death by starvation or deh ...
Explaining density-dependent regulation in earthworm populations
Explaining density-dependent regulation in earthworm populations

... the fact that they play an important role in food web dynamics and contribute to nutrient cycling and decomposition processes (DeRuiter et al. 1995). Amongst the few studies that have been conducted, Bengtsson et al. (1994) reported on the density-dependent dispersal of springtails and Klironomos an ...
chapter 1
chapter 1

... In the natural world, many species have a life history that takes their individual members through two stages: immature and mature with a time lag. In ecology, more realistic models should include some of the past states of the system: that is, ideally, a real system should be modeled by differentia ...
The Effects of Simulated Competition on Foraging Behavior in
The Effects of Simulated Competition on Foraging Behavior in

... Ecological communities are often shaped by competition between individuals for a shared limited resource (Rohde 2011). Competition may be between individuals of the same species (intraspecific competition) or between individuals of different species (interspecific competition). In forest communities ...
as a PDF
as a PDF

... more general expression—including variation in intraspecific interactions—establishes the relationship between the distributions of a and K and the abundance distribution of all species. Figure 1a compares results from the analytic target distributions with results from numerical integrations for th ...
Patch Disturbance and the Human Niche by John M - Zoe-s-wiki
Patch Disturbance and the Human Niche by John M - Zoe-s-wiki

... species enter the community. Others are extirpated (ie-become locally extinct). Species which dominated a landscape at one time become minor components of the community while other species are "fruitful and multiply", becoming dominant species. This change is in some way directional and generally pr ...
POPULATIONS
POPULATIONS

A General Approach to the Modelling of Trophic Chains
A General Approach to the Modelling of Trophic Chains

... human populations (Banks, 1994) and, when generalized, describes the dynamics of many single species populations in both laboratory and field (Gause, 1934; Allee et al., 1949; Thomas et al., 1980; Berryman and Millstein, 1990). It is applicable to multiple situations in ecology and biology (Banks, 1 ...
Lifehistory constraints in grassland plant species: a growthdefence
Lifehistory constraints in grassland plant species: a growthdefence

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Storage effect

The storage effect is a coexistence mechanism proposed in the ecological theory of species coexistence, which tries to explain how such a wide variety of similar species are able to coexist within the same ecological community or guild. The storage effect was originally proposed in the 1980s to explain coexistence in diverse communities of coral reef fish, however it has since been generalized to cover a variety of ecological communities. The theory proposes one way for multiple species to coexist: in a changing environment, no species can be the best under all conditions. Instead, each species must have a unique response to varying environmental conditions, and a way of buffering against the effects of bad years. The storage effect gets its name because each population ""stores"" the gains in good years or microhabitats (patches) to help it survive population losses in bad years or patches. One strength of this theory is that, unlike most coexistence mechanisms, the storage effect can be measured and quantified, with units of per-capita growth rate (offspring per adult per generation).The storage effect can be caused by both temporal and spatial variation. The temporal storage effect (often referred to as simply ""the storage effect"") occurs when species benefit from changes in year-to-year environmental patterns, while the spatial storage effect occurs when species benefit from variation in microhabitats across a landscape.
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