Experimental analysis reveals that individual stage and culling levels significantly affect extinction probabilities in populations of Collembola, suggesting complex dynamics at play.
Predicting the fate of small populations is essential in ecology, epidemiology and conservation biology. Small populations can go extinct quickly or can develop into large established populations. These can still go extinct through demographic stochasticity, especially when declines in mean population size or large size fluctuations drive them into an extinction vortex. Individual differences and environmental conditions are two factors expected to determine extinction probabilities in recently founded populations. In populations surviving this initial phase, effects of initial conditions are expected to wash out, unless these differences in conditions persist systematically. We used the parthenogenetic Collembola Folsomia candida to investigate such effects in a crossed treatment on 290 replicate populations, each initiated with a single individual. Populations were initiated with founders of three different life stages and subjected to four levels of culling. Their extinction times were recorded in a period of up to 41 weeks after initiation. We fitted the parameters of an age‐structured multi‐type branching process model to extinction rates observed in the first weeks after initiation. As predicted by the model, extinction probabilities increased with the level of culling. Populations started by non‐reproducing individuals had larger extinction probabilities which decreased over time. In established populations, extinction probabilities increased with culling levels, and the effects of the founder stage disappeared, except for a late increase in extinction probability in populations founded by newborns. This increase was not expected and forced us to reconsider when transient effects of the initial state would end. We hypothesize that size‐structured competition in this system causes long‐term transients. The results show that predictors of extinction probability can be shared between small and established populations. Transient dynamics of extinction risk can be long, with phases even mimicking a stationarity followed by the onset of an extinction vortex.
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Bakker et al. (2025) studied this question.
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