The discrete-time recursion system un+1 = Q[un] with un(x) a vector of population distributions of species and Q an operator which models the growth, interaction, and migration of the species is considered. Previously known results are extended so that one can treat the local invasion of an equilibrium of cooperating species by a new species or mutant. It is found that, in general, the resultin...

Alien plant invaders significantly threaten native community diversity, although it is poorly understood whether invasion initiates a linear or non-linear loss of resident species. Where low abundances of an invader have little impact on native species diversity, then a threshold level may exist, above which native communities rapidly decline. Our aim was to assess the broadscale effects of an ...

Mismatches between invasive species management policies and ecological knowledge can lead to profound societal consequences. For this reason, natural resource agencies have adopted the scientifically-based density-impact invasive species curve to guide invasive species management. We use the density-impact model to evaluate how well management policies for a native invader (Juniperus virginiana...

Soil organisms influence plant species coexistence and invasion potential. Plant-soil feedbacks occur when plants change soil community composition such that interactions with that soil community in turn may positively or negatively affect the performance of conspecifics. Theories predict and studies show that invasions may be promoted by stronger negative soil feedbacks for native compared wit...

There is a trade-off between nitrogen (N) allocation to photosynthesis and to defence. Invasive species may reduce N allocation to defence because of the absence of natural enemies. Thus, I hypothesised that invasive species may allocate a higher fraction of total leaf N to photosynthesis and have higher light-saturated photosynthetic rate (P(max)) and photosynthetic N-use efficiency (PNUE) tha...

The effects of declining plant biodiversity on ecosystem processes are well studied, with most investigations examining the role of species richness declines rather than declines of species abundance. Using grassland mesocosms, we examined how the abundance of a native, resident species, Hemizonia congesta (hayfield tarweed), affected exotic Centaurea solstitialis (yellow starthistle) invasion....

Bemisia tabaci (Hemiptera: Aleyrodidae) is a globally distributed pest composed of at least 34 morphologically indistinguishable cryptic species. At least seven species of endosymbiont have been found infecting some or all members of the complex. The origin(s) of the associations between specific endosymbionts and their whitefly hosts is unknown. Infection is normally vertical, but horizontal t...

In a microcosm experiment, I tested how species composition, species richness, and community age affect the susceptibility of grassland communities to invasion by a noxious weed (Centaurea solstitialis L.). I also examined how these factors influenced Centaurea’s impact on the rest of the plant community. When grown in monoculture, eight species found in California’s grasslands differed widely ...

Invaded systems are commonly associated with a change in ecosystem processes and a decline in native species diversity; however, many different causal pathways linking invasion, ecosystem change, and native species decline could produce this pattern. The initial driver of environmental change may be anthropogenic, or it may be the invader itself; and the mechanism behind native species decline ...

Biological control using natural antagonists has been a most successful management tool against alien invasive plants that threaten biodiversity. The selection of candidate agents remains a critical step in a biocontrol program before more elaborate and time-consuming experiments are conducted. Here, we propose a biogeographic approach to identify candidates and combinations of candidates to po...