by Eric Janney » Wed May 21, 2008 6:57 pm
The estimated variance associated with the Phi(t) model in a CJS is a combination of sampling variance and the process variance. The process variance is an estimate of the actual temporal variability in survival. For a PVA analysis it is important to only include the process variance. It is common in PVA analyses for people to incorrectly use a variance estimate that includes sampling variance. So, how do you tease variance due to sampling error from process variance? There are several good papers that discuss methods for estimating process variance.
Gould, W. R., J. D. Nichols. 1998. Estimation of temporal variability of survival in animal populations. Ecology, 79 (7), pp. 2531-2538.
Burnham, K.P, and G.C. White. 2002. Evaluation of some random effects methodology applicable to bird ringing data. Journal of Applied Statistics, 2002, vol. 29, issue 1–4, pages 245–264
Link, W. A., and J. D. Nichols. 1994. On the importance of sampling variance to investigations of temporal variation in animal population size. Oikos 69: 539-544.
These methods are commonly referred to as variance components and the methods described by Burnham and White (2002) are incorporated in MARK. There is also a Bayesian method called MCMC that is also in MARK. There is a fair amount of literature on MCMC as well, but I don't have the references offhand. Anyway, I hope this helps.