phylo() is a unified entry point for the package's five canonical
phylogenetic keywords (phylo_scalar, phylo_unique, phylo_indep,
phylo_latent, phylo_dep). It accepts an lme4-bar formula on the
first argument and dispatches to the appropriate canonical keyword
based on the LHS shape and the optional mode = ... argument. The
five canonical keywords stay first-class — phylo() is an additive
alias matching the lme4 / brms / drmTMB convention.
Arguments
- formula
An lme4-bar formula (
<lhs> | <species_column>) OR, for backward-compat, a bare unquoted column name (legacy form). The bar's RHS is the species factor; the LHS determines the covariance structure (combined withmode, see Dispatch rules).- tree
An
ape::phyloobject. Canonical. Sparse \(\mathbf A^{-1}\) via Hadfield & Nakagawa (2010).- vcv
A tip-only phylogenetic correlation matrix (
n_species x n_species). Legacy / superseded.- mode
One of
"scalar"/"diag"/"indep"/"latent"/"dep". Optional when LHS is1(defaults silently to"scalar"). Mandatory when LHS is0 + trait.- d
Latent rank for
mode = "latent". Default 1.
Dispatch rules
| Form | Mode default | Rewrites to |
phylo(1 \| species) | "scalar" | phylo_scalar(species) |
phylo(0 + trait \| species, mode = "diag") | (mandatory) | phylo_unique(species) |
phylo(0 + trait \| species, mode = "indep") | (mandatory) | phylo_indep(0 + trait \| species) |
phylo(0 + trait \| species, mode = "latent", d = K) | (mandatory) | phylo_latent(species, d = K) |
phylo(0 + trait \| species, mode = "dep") | (mandatory) | phylo_dep(0 + trait \| species) |
When the LHS expands to a single column (1, intercept-only), mode
is degenerate: it defaults silently to "scalar", and explicit
mode = "scalar" is accepted (no warning). When the LHS is
0 + trait, mode is mandatory — choosing between "diag" /
"indep" / "latent" / "dep" is a meaningful decision (per-trait
diagonal vs reduced-rank decomposition vs full unstructured) and the
parser refuses to silently default.
Backward compatibility
Legacy bare-name calls phylo(species) and phylo(species, vcv = Cphy)
continue to work as deprecated aliases of phylo_scalar(species) /
phylo_scalar(species, vcv = Cphy). The legacy form rewrites to
propto(0 + species | trait) internally, picking up the phylogenetic
covariance from the top-level phylo_vcv = argument to gllvmTMB().
Augmented LHS (Stage 3, not yet shipped)
Augmented LHS forms — 1 + x (intercept + slope), 0 + trait + (0 + trait):x
(per-trait intercepts + per-trait slopes on covariate x), x || species
(uncorrelated) — are reserved for Design 07 Stage 3 engine work. The
parser currently raises an error pointing at this status.
Cross-package coexistence
drmTMB also exposes phylo(1 | species, tree = tree) with the same
Hadfield–Nakagawa sparse \(\mathbf A^{-1}\) internal path. Both
packages share the same calling convention; user muscle memory
transfers.
Examples
if (FALSE) { # \dontrun{
library(ape)
tree <- rcoal(20); tree$tip.label <- paste0("sp", 1:20)
# Single shared phylogenetic variance (= phylo_scalar)
fit_s <- gllvmTMB(value ~ 0 + trait + phylo(1 | species, tree = tree),
data = df)
# Per-trait phylogenetic variances on shared A (= phylo_unique)
fit_u <- gllvmTMB(value ~ 0 + trait +
phylo(0 + trait | species, mode = "diag", tree = tree),
data = df)
# Reduced-rank cross-trait phylogenetic decomposition (= phylo_latent)
fit_l <- gllvmTMB(value ~ 0 + trait +
phylo(0 + trait | species, mode = "latent",
d = 2, tree = tree),
data = df)
# Backward-compat: legacy bare-name form
Cphy <- vcv(tree, corr = TRUE)
fit_legacy <- gllvmTMB(value ~ 0 + trait + phylo(species),
data = df, phylo_vcv = Cphy)
} # }
