The Spatial and Temporal Dynamics of Host-Parasitoid Interactions

By M. Hassell. 2000

407 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/10596430abd2bb63520bdc3fed5d8423dd554202

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In Insect Science

Citations in the corpus

Effects of habitat fragmentation at different trophic levels in insect communities (2005, background): “As long as habitat fragmentation is not too extreme, fragmentation can promote regional coexistence of predators and prey (Hassell 2000, Holt 2002), and its effect can differ greatly among species.”
Allee Effects in Ecology and Conservation (2008, background): “For example, searching efficiency of a predator may decrease and/or handling time of prey may increase with increasing predator density (Hassell 2000).”
Indirect effects between shared prey: Predictions for (2004, background): “Equivalent single predator–single prey systems are locally unstable if nonoverlapping generations are modeled with discrete equations (Hassell, 2000), and the stability properties again do not change in the two-prey system.”
The Functional Response of Parasitoids and its Implications for Biological Control (2003, background): “For instance, when the time delays are reduced or absent, as in continuous models (Murdoch & Oaten, 1975) or when the parasitoids’ dynamics are uncoupled from those of their hosts (Hassell, 2000).”
MATRIX HETEROGENEITY AND HOST–PARASITOID INTERACTIONS IN SPACE (2003, background): “Among the numerous theoretical studies of predator– prey dynamics, the consensus is that spatial heterogeneity can significantly affect the temporal dynamics, stability, and spatial distribution of populations (reviewed in Tilman and Kareiva 1997, Hanski 1999, Hassell 2000).”
The physiology of host feeding in parasitic wasps: implications for survival (2002, unknown): “…are excellent models for testing theories concerning the evolution of behaviour and life-history strategies (Charnov & Skinner 1984; Charnov & Skinner 1985; Godfray 1994; Quicke 1997) and for integrating such knowledge into multitrophic population ecology (Hochberg & Ives 2000; Hassell 2000).”
Ratio dependence in the functional response of insect parasitoids: evidence from Trichogramma minutum foraging for eggs in small host patches (2004, methodology): “Mutual interference as a form of parasitoid dependence in the functional response of insect parasitoids also has a strong legacy (Hassell, 1978, 2000); however, Arditi and Akçakaya (1990) point out that mutual interference (m) has often been underestimated in the analysis of laboratory data from…”
Plant-insect interactions in fragmented landscapes. (2004, background): “Interactive communities Competitive coexistence (110) Space enables coexistence of prey and (66, 72) predators Habitat fragmentation leads to shorter (72, 73) chains in food webs Apparent competition (72) Habitat fragmentation increases ratio of (72, 79) habitat generalists to specialists Complex sp”
The wolves of Isle Royale display scale-invariant satiation and ratio-dependent predation on moose (2005, background): “Such high values of m have occasionally been reported in field studies of various systems (Hassell 1978, 2000; Sutherland 1996; Ponsard et al. 2000; Jost & Arditi 2001) but they are puzzling because m > 1 indicates overcompensating interference: the whole wolf pack captures less moose as the pack…”
Population biology of entomopathogenic nematodes: Concepts, issues, and models (2006, background): “The mathematical ecology of host–parasitoid interactions is well developed (Hassell, 2000) and underlies the formulation of our model.”
Colonization rates and distances of a host butterfly and two specific parasitoids in a fragmented landscape (2002, unknown): “There is an extensive theoretical literature on models of both competitive and host–parasitoid (predator–prey) interactions involving dispersal within a continuous habitat or among discrete habitat patches (reviews in Nee, May & Hassell 1997; Hassell 2000).”
Ecological Networks in a Changing Climate (2010, background): “The population dynamics of host–parasitoid interactions have been studied extensively (Hassell, 2000) and models of pair-wise species interactions have been extended to describe the dynamics of at least simple experimental communities very successfully (Bonsall and Hassell, 1998; van Veen et al.”