by abreton » Mon Oct 31, 2011 1:17 pm
I assume phi4 and phi5 are still giving you trouble in these models? Assuming covariate 1 and 2 are not strongly correlated (if they are then drop one of these from your analysis), then, assuming CJS was the most appropriate parameterization for your data, then I would likely proceed by building all possible models including cov1, cov2 and weight. If biology (and the data) supported 2-way (or 3-way) interactions then I'd incorporate these interactions into the all possible models. See MARK Menu, Run>Subset of DM Models for a quick solution for building 'all possible'.
No doubt several models would be within ca. 6 AICc units. I'd proceed by model averaging...and make inferences based on the model averaged (unconditional) estimates of the parameters. For the cov1 and cov2 effects, I'd also model average betas associated with these effects and use a log odds ratio to quantify/visualize effect size.
I've never used the model deviance to make inferences about explained variance...and note, I don't think you could say 'weight' is responsible for the realized deviance unless you compare models without weight.
andre
Last edited by
abreton on Tue Nov 01, 2011 3:50 pm, edited 1 time in total.