assocs: A matrix of association strengths among two sets of interacting species
tree1: A phylo tree object or a phylogenetic covariance matrix for the rows of assocs
tree2: A phylo tree object or a phylogenetic covariance matrix for the columns of assocs
covars1: A matrix of covariates (e.g., traits) for the row species of assocs
covars2: A matrix of covariates (e.g., traits) for the column species of assocs
bootstrap: logical, bootstrap confidence intervals of the parameter estimates
nreps: Number of bootstrap replicated data sets to estimate parameter CIs
maxit: as in optim
pstart: starting values of the two phylogenetic signal strength parameters passed to optim
x: object of class pblm
tree1.w.novel: A phylo tree object or a phylogenetic covariance matrix which corresponds to tree1 of x with species to predict associations
tree2.w.novel: A phylo tree object or a phylogenetic covariance matrix which corresponds to tree2 of x with species to predict associations
predict.originals: if TRUE then the associations of each original species in the two phylogenies is predicted
Details
Fit a linear model with covariates using estimated generalized least squares to the association strengths between two sets of interacting species. Associations can be either binary or continuous. If phylogenies of the two sets of interacting species are supplied, two phyogenetic signal strength parameters (d1 and d2), one for each species set, based on an Ornstein-Uhlenbeck model of evolution with stabilizing selection are estimated. Values of d=1 indicate no stabilizing selection and correspond to the Brownian motion model of evolution; 0<d<1 represents stabilizing selection; d=0 depicts the absence of phylogenetic correlation (i.e., a star phylogeny); and d>1 corresponds to disruptive selection where phylogenetic signal is amplified. Confidence intervals for these and the other parameters can be estimated with bootstrapping.
The function pblmpredict predicts the associations of novel species following the methods given in appendix B of Ives and Godfray (2006).
Returns
MSE: total, full (each d estimated), star (d=0), and base (d=1) mean squared errors
signal.strength: two estimates of phylogenetic signal strength
coefficients: estimated intercept and covariate coefficients with approximate 95 percent CIs for the three model types (full, star, base)
CI.boot: 95 percent CIs for all parameters
variates: matrix of model variates (can be used for plotting)
residuals: matrix of residuals from the three models (full, star and base)
predicted: predicted associations
bootvalues: matrix of parameters estimated from the nreps bootstrap replicated data sets used to calculate CIs
phylocovs: phylogenetic covariance matricies scaled by the estimated d1 and d2
cors.1: correlations among predicted and observed associations for species of tree1, NA if predict.originals=FALSE
cors.2: correlations among predicted and observed associations for species of tree2, NA if predict.originals=FALSE
pred.novels1: predicted associations for the novel speices of tree1
pred.novels2: predicted associations for the novel speices of tree2
Note
Covariates that apply to both species sets (e.g., sampling site) should be supplied in the covariate matrix of the set with the most species.
Bootstrapping CIs is slow due to the function optim used to estimate the model parameters. See appendix A in Ives and Godfray (2006) for a discussion about this boostrapping procedure
If pblmpredict=TRUE the function does not first remove each species in turn when predicting the associations of the original species as is done in Ives and Godfray (2006).
References
Ives A.R. & Godfray H.C. (2006) Phylogenetic analysis of trophic associations. The American Naturalist, 168, E1-E14
Blomberg S.P., Garland T.J. & Ives A.R. (2003) Testing for phylogenetic signal in comparative data: Behavioral traits are more labile. Evolution, 57, 717-745
#load example data from Ives & Godfray (2006)data(IvesGodfray)#net attack rate of parasitoid on host eq.4 in Ives and GodfrayA<-(-1*log(1-IvesGodfray$interactions[,-28]/t(IvesGodfray$interactions[28])))# Make tips of the phylogenetic trees contemporaneous by extending tipsp<-dim(IvesGodfray$host)[1]q<-dim(IvesGodfray$parasitoid)[1]host.cov.scaled<-IvesGodfray$host
para.cov.scaled<-IvesGodfray$parasitoid
for(i in1:p){ host.cov.scaled[i,i]<-max(host.cov.scaled)}for(i in1:q){ para.cov.scaled[i,i]<-max(para.cov.scaled)}# scale covariance matrices (this reduces numerical problems caused by# determinants going to infinity or zero) host.cov.scaled<-host.cov.scaled/(det(as.matrix(host.cov.scaled))^(1/p)) para.cov.scaled<-para.cov.scaled/(det(as.matrix(para.cov.scaled))^(1/q))pblm.A <- pblm(sqrt(A),tree1=host.cov.scaled,tree2=para.cov.scaled)pblm.A$signal.strength #compare to Ives and Godfray (2006) Table 1 Line 1pblm.A$MSE