Hi Christy,
I think the important first question is how does PGLS change the conclusions you would make with OLS? You can compare coefficients, or compare SS, MS, or R2 in your ANOVA tables, or maybe compare fitted values from both. Here’s an idea, use two.b.pls to see how associated fitted values are from each. If this correlation is high, or the ANOVA tables are similar (i.e., significant effects did not become non-significant after PGLS), then you can do the normal OLS pairwise comparisons with the ability to indicate that it’s okay to ignore phylogeny (if that is what your examination indicates). If your effects were rendered non-significant due to phylogeny, there would be little sense in pairwise comparisons, anyway.
To my way of thinking, phylogenetic “correction” is a first-order problem. One does PGLS to ascertain if the same interpretations can be made after adjusting OLS coefficients (does ANOVA tell us the same thing?) I suppose that there is a case where a significant ANOVA from OLS leads to e.g., 4 out of 6 pairwise comparisons that are significant and the still significant effect in PGLS might lead to only 2 out of 6 significant pairwise comparisons. But in most cases, it is probably sufficient to simply ask if significant sources of variation remain significant after PGLS? If so, go back to OLS and break things down further.
You mention between-group PCA. This can be done easily with PGLS-fitted values, just like OLS-fitted values. This is analogous to doing pairwise comparisons in a visual sense - just no P-values added to the distances between groups. Caution! Do not attempt to use PC scores from such an analysis for pairwise tests though. This test would confound phylogeny and group differences in generating probability distributions. We discussed this problem here:
http://www.public.iastate.edu/~dcadams/PDFPubs/2015-Evol-AdamsCollyer-PIC-PGLS%20Shuffle.pdf
You also mention CVA… I would stay away from this in the PGLS sense. One can get canonical axes after PGLS, project data onto them, and make plots, and that is fine. But if one takes it a step further and tries to classify subjects, trouble could ensue, especially if using canned CVA/DFA programs. The lda function in R is not so bad, because one can input prior probabilities. I believe the CVA function in MorphoJ, for example, does not allow one to alter prior probabilities (it either assumes equal priors or bases them on group sizes - maybe somebody can correct me if I am wrong). But it would be unfortunate to not have priors informed by phylogenetic relatedness. We discussed this a bit here:
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0146166
good luck!
Mike
Hi Mike,
Thanks for your response. It sounds like the test will have to wait. I’m only concerned that a reviewer will immediately demand it, since I get the impression that everyone expects phylogenetic comparative tests now even without knowing what they really produce. I can’t say how many times I’ve been asked to run a phylogenetic PCA, even though it’s been shown that it doesn’t do at all what one expects (create independent axes, relate back to the shape variables, etc). I could show the standard pairwise comparisons instead, plus I also have CVA and between-group PCA to identify where and what the main differences between groups are. Hopefully that will suffice!
Thanks again,
Christy
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