Dear Julien, maybe I dont understand your rmodel...but IF your model has one continuous dep. and one categorical (binary) indep. it looks like an ANOVA model: in this case phy.anova() [or phy.manova() if you have >1 dependents] in the R package geiger does it. IF the model is different .......please explain better. Inverting the dependence-independence relationship....depends on your hypothesis testing. When the categorical becomes the dependent you need to apply a phylogentic logistic regression (in the case of binary) or multinomial logistic (I think MCMCglmm does it).
IF you have more factor variables as dependent...applying comparative methods maybe is more complicated but a trick could be useful. Say you have a two-levels and a four levels factor variables. You can test ***** pairwise *****(!!) your (**CONTINUOUS**!!) dependent against a new factor where you coded any possible level identifiable by all occurring combinations of the levels of the two factor variables. Not necessarily there will be a n°levels equal to the n°levels of fisrt factor variable * n°levels of the second one: it depends from real data. But you wrote: "symbiont location ~ habitat VS habitat ~ symbiont location" here....all things are categorical....is it?...Where is the body size? Best Paolo Dear colleagues, I am testing the impact of categorical binary characters (habitat and presence/absence of symbionts) on a continuous variable (log of body size) using PGLS... I am not sure if I should remove the intercept from the formulae and the biological interpretation of the absence of intercept for categorical variables.. All papers I found on the issue of regression through origin were about PIC and continuous characters It does not change my conclusions when I test individually each variable (BOTH have a HIGHLY significant impact on body size), but it does when I test them simultaneously: Coefficients: Estimate Std. Error t value Pr(>|t|) (Intercept) 3.252335 0.731056 4.4488 5.115e-05 *** Habitat1 0.706823 0.434013 1.6286 0.1099 Location1 0.598868 0.810679 0.7387 0.4637 Habitat1:Location1 -0.078772 0.905514 -0.0870 0.9310 F-statistic: 3.744 on 4 and 48 DF, p-value: 0.009906 Coefficients: Estimate Std. Error t value Pr(>|t|) Habitat0 3.252335 0.731056 4.4488 5.115e-05 *** Habitat1 3.959158 0.782851 5.0574 6.629e-06 *** Location1 0.598868 0.810679 0.7387 0.4637 Habitat1:Location1 -0.078772 0.905514 -0.0870 0.9310 F-statistic: 3.744 on 4 and 48 DF, p-value: 0.009906 Also, the output of the above analysis depends on the order of variables (symbiont location ~ habitat VS habitat ~ symbiont location).. Once the effect of one variable is removed, the effect of the other one is no longer significant, likely because both are correlated. Is there an objective way to decide which one explains the best the body size ? Perhaps considering amount of variance explained by each variable individually ? Apologies for these very naive questions.. I guess answers are obvious to most of you but... Thanks in advance for your comments. Regards Julien Lorion PhD, Post-doctoral fellow of the Japan Society for the Promotion of Science Japan Agency for Marine-Earth Science and Technology (JAMSTEC) Marine Ecosystems Research Department 2-15 Natsushima, Yokosuka 237-0061 Japan Phone: +81-46-867-9570, Fax: +81-46-867-9525 [[alternative HTML version deleted]] _______________________________________________ R-sig-phylo mailing list R-sig-phylo@r-project.org https://stat.ethz.ch/mailman/listinfo/r-sig-phylo -- Paolo Piras Center for Evolutionary Ecology and Dipartimento di Scienze Geologiche, Università Roma Tre Largo San Leonardo Murialdo, 1, 00146 Roma Tel: +390657338000 email: ppi...@uniroma3.it _______________________________________________ R-sig-phylo mailing list R-sig-phylo@r-project.org https://stat.ethz.ch/mailman/listinfo/r-sig-phylo