scholarly journals Exploring population responses to environmental change when there's never enough data; a factor analytic approach

2017 ◽  
Author(s):  
Bethan J. Hindle ◽  
Mark Rees ◽  
Andy W. Sheppard ◽  
Pedro F. Quintana-Ascencio ◽  
Eric S. Menges ◽  
...  

Temporal variability in the environment drives variation in individuals' vital rates, with consequences for population dynamics and life history evolution. Integral projection models (IPMs) are data-driven models widely used to study population dynamics and life history evolution of structured populations in temporally variable environments. However, many data sets have insufficient temporal replication for the environmental drivers of vital rates to be identified with confidence, limiting their use for evaluating population level responses to environmental change. Parameter selection, where the kernel is constructed at each time step by randomly selecting the time-varying parameters from their joint probability distribution, is one approach to including stochasticity in IPMs. We consider a factor analytic (FA) approach for modelling the covariance matrix of time-varying parameters, whereby latent variable(s) describe the covariance among vital rate parameters. This decreases the number of parameters estimated and, where the covariance is positive, the latent variable can be interpreted as a measure of environmental quality. We demonstrate this using simulation studies and two case studies. The simulation studies suggest the FA approach provides similarly accurate estimates of stochastic population growth rate to estimating an unstructured covariance matrix. We demonstrate how the latent parameter can be perturbed to show how selection on reproductive delays in the monocarp Carduus nutans changes under different environmental conditions. We develop a demographic model of the fire dependent herb Eryngium cuneifolium to show how a causal indicator (i.e. a driver of the changes in the environmental quality) can be incorporated with the addition of a single parameter. Using perturbation analyses we determine optimal management strategies for this species. This approach estimates fewer parameters than previous approaches and allows novel eco-evolutionary insights. Predictions on population dynamics and life history evolution under different environmental conditions can be made without necessarily identifying causal factors. Environmental drivers can be incorporated with relatively few parameters, allowing for predictions on how populations will be affected by changes to these drivers.

2015 ◽  
Vol 103 (4) ◽  
pp. 798-808 ◽  
Author(s):  
Jennifer L. Williams ◽  
Hans Jacquemyn ◽  
Brad M. Ochocki ◽  
Rein Brys ◽  
Tom E. X. Miller

2009 ◽  
Vol 364 (1523) ◽  
pp. 1499-1509 ◽  
Author(s):  
Shripad Tuljapurkar ◽  
Jean-Michel Gaillard ◽  
Tim Coulson

Environmental stochasticity is known to play an important role in life-history evolution, but most general theory assumes a constant environment. In this paper, we examine life-history evolution in a variable environment, by decomposing average individual fitness (measured by the long-run stochastic growth rate) into contributions from average vital rates and their temporal variation. We examine how generation time, demographic dispersion (measured by the dispersion of reproductive events across the lifespan), demographic resilience (measured by damping time), within-year variances in vital rates, within-year correlations between vital rates and between-year correlations in vital rates combine to determine average individual fitness of stylized life histories. In a fluctuating environment, we show that there is often a range of cohort generation times at which the fitness is at a maximum. Thus, we expect ‘optimal’ phenotypes in fluctuating environments to differ from optimal phenotypes in constant environments. We show that stochastic growth rates are strongly affected by demographic dispersion, even when deterministic growth rates are not, and that demographic dispersion also determines the response of life-history-specific average fitness to within- and between-year correlations. Serial correlations can have a strong effect on fitness, and, depending on the structure of the life history, may act to increase or decrease fitness. The approach we outline takes a useful first step in developing general life-history theory for non-constant environments.


1996 ◽  
Vol 351 (1345) ◽  
pp. 1349-1359 ◽  

Analysis of life history evolution in spatially heterogeneous environments was revolutionized by the demonstration by Kawecki & Stearns (1993) and Houston & McNamara (1992) that earlier treatments had used incorrect fitness measures. The implications of this for the analysis of organisms with and without phenotypic plasticity are reviewed. It is shown that analyses ignoring age structure can give misleading results. The plausibility and implications of the assumptions are discussed, and suggestions are made for further work. The usefulness of reciprocal transplant and common garden experiments, in providing information relevant to the assumptions and predictions, is emphasized. Two simulation studies show that life history evolution in temporally heterogeneous environments in which trade-offs are fixed are well predicted by Schaffer’s (1974) model, with modification for asymmetric variations as necessary. Unfortunately the period of study needed to observe such effects is so long as to preclude experimental tests for most organsims.


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