Demography |
Stable stage-structure theory |
Individual traits averaged |
Relevant individual traits maintained |
Lack of coherent theory |
Disease Ecology |
Coherent invasion and burnout theory |
Limited account of superspreaders and variation in susceptibility |
Unlimited account of variation in transmission and susceptibility |
Difficult to generalize among diseases |
Movement Ecology |
Provides highly aggregated overview of population movement |
Cannot account for movement at fine spatio-temporal scales |
Can relate fine scale movements to local landscape factors |
Theory of scaling up individual movements to population level needed |
Behavioral Ecology |
Simple fitness maximization theories possible: e.g. optimal foraging |
Ignores fact that behavior is often highly heterogeneous at the individual level |
Can account for heterogeneity of behavior at the individual level |
More care is needed to handle the complexity of fitness maximizing theories |
Trophic Ecology |
Allows first order effects (averages) to be clearly assessed |
Variation in resources available to individuals largely ignored |
Critical effects due resource variation can be incorporated |
Enormity of computations may be overwhelming if not handled carefully |
Evolutionary Ecology |
Well developed gene-for-trait and coalescence theory models exists |
Links between genetic and ecological heterogeneity hard to make |
Easy to link genetic and ecological heterogeneity |
Hard to characterize emergent properties and processes responsible for speciation |