The vitality-based survival model is a parametric model for relating stressors and environmental properties to organism survivorship. Vitality is an abstract property which changes in response to organism experience. An organism's resistance to disease, level of stress, behavior, success and failure in feeding, frequency of predator attack, mating, parental care, and habitat choice all induce incremental changes in vitality. Mortality occurs when an organism's vitality reaches zero. Mortality can also occur independent of vitality through accidental-based mortality; catastrophic events occurring equally within a population and independent of the different past histories of the individuals. The model survival distribution is then the product of the probability of survival according to the organism's vitality and the probability of avoiding accidental mortality.
Four (4) Parameter Vitality Model
Li, T. and J.J. Anderson. 2009. The vitality model: A way to understand population survival and demographic heterogeneity. Theoretical Population Biology, In Press, Corrected Proof, Available online 3 June 2009, ISSN 0040-5809, DOI: 10.1016/j.tpb.2009.05.004.
Abstract
Anderson, J.J., M.C. Gildea, D.W. Williams, and T. Li. 2008. Linking Growth, Survival, and Heterogeneity through Vitality. The American Naturalist. 171: E20-E43.
Abstract
4 Parameter Model R Code and Data, June 2009
The supplemental R script file vitality.gaussian.R contains all functions necessary to run the MLE parameter fitting routine for the vitality-based survival model (Li and Anderson 2009) with an initial Gaussian distribution. The functions are written in the R programming language. Most of the functions are very similar to those written by Salinger et al. (2003) in S-plus for fitting the vitality model with a Dirac delta function initial distribution. The fitting routines differ in how they derive initial parameter estimates for the Newton-Ralphson method.
R Statistical Package
R Project for Statistical Computing. R is a free software environment for statistical computing and graphics. It compiles and runs on a wide variety of UNIX platforms, Windows and MacOS.
Three (3) Parameter Vitality Model
Salinger, D.H., J.J. Anderson, and O.S. Hamel. 2003. A parameter estimation routine for the vitality-based survival model. Ecological Modelling 166(3): 287-294.
Abstract
Anderson, J.J. 2000. A vitality-based model relating stressors and environmental properties to organism survival. Ecological Monographs 70(3): 445-470.
Abstract
A survivorship curve is shaped by the differential survivability of the organisms within the population, and a change in a survivorship curve with a stressor reflects the differential response of the organisms to the stressor. Quantifying this linkage in a simple, rigorous way is valuable for characterizing the response of populations to stressors and ultimately for understanding the evolutionary selection of individuals exposed to stressors. To quantify this stressor-individual-population linkage with as few parameters as possible, I present a simple mechanistic model describing organism survival in terms of age-dependent and age-independent mortality rates. The age-independent rate is represented by a Poisson process. For the age-dependent rate, a concept of vitality is defined, and mortality occurs when an organism's vitality is exhausted. The loss of vitality over age is represented by a continuous Brownian-motion process, the Weiner process; vitality-related mortality occurs when the random process reaches the boundary of zero vitality. The age at which vitality-related mortality occurs is represented by the Weiner-process probability distribution for first-arrival time. The basic model has three rate parameters: the rate of accidental mortality, the mean rate of vitality loss, and the variability in the rate of vitality loss. These rates are related to body mass, environmental conditions, and xenobiotic stressors, resulting in a model that characterizes intrinsic and extrinsic factors that control a population's survival and the distribution of vitality of its individuals. The model assumes that these factors contribute to the rate parameters additively and linearly.
The model is evaluated with case studies across a range of species exposed to natural and xenobiotic stressors. The mean rate of vitality loss generally is the dominant factor in determining the shape of survival curves under optimal conditions. Xenobiotic stressors add to the mean rate in proportion to the strength of the stressor. The base, or intrinsic, vitality loss rate is proportional to the -1/3 power of adult body mass across a range of iteroparous species. The increase in vitality loss rate with a xenobiotic stressor can be a function of body mass according to the allometric relationship of the organism structures affected by the stressor. The model's applicability to dose–response studies is illustrated with case studies including natural stressors (temperature, feeding interval, and population density) and xenobiotic stressors (organic and inorganic toxicants). The model provides a way to extrapolate the impact of stressors measured in one environment to another environment; by characterizing how stressors alter the vitality probability distribution, it can quantify the degree to which a stressor differentiates members of a population.
3 Parameter Model S-PLUS Code and Data, March 2003, December 2004 update
The algorithm determines model parameters for the vitality-based survival model (Anderson 2000). The algorithm uses an MLE estimator on interval-based survival data and returns the vitality model parameters: the rate of vitality loss, the variability in the rate of vitality loss and the rate of accidental mortality. Standard errors of the parameter estimates and a Goodness-of-fit measure (via a Pearson's C test) are also returned. Issues of right censored data and study start time are addressed.
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