We have extended our studies of angiosperm phylogeny based on a pair of dup
licated phytochrome (PHY) genes, PHYA and PHYC. Phylogenetic analyses of se
quences from 52 species yield unrooted gene networks in which all of the el
ements resolved in our previous analysis of 26 species appear. Amborella st
ill emerges as the sister group of all other angiosperms. However, we canno
t reject alternative rootings in which water lilies, either alone or in com
bination with Amborella, are basal. Austrobaileya + Illicium diverges next
from the remaining angiosperms. Eudicots and monocots form rather well-supp
orted clades, as do Magnoliales, Laurales, Piperales, and winteroids, but r
elationships among these major lineages remain uncertain, as do the positio
ns of Chloranthaceae and Ceratophyllum. Magnoliales may be directly linked
with Laurales and Piperales with winteroids, but support for these relation
ships is not strong. Within eudicots, a basal split between ranunculids (Ra
nunculales, Papaverales) and the rest of the eudicots is supported, though
the position of Nelumbo is equivocal. These same relationships are obtained
in combined analyses of PHYA and PHYC (species as terminals) when Ceratoph
yllum is excluded. However, when Ceratophyllum is included, Austrobaileya Illicium and then Chloranthaceae diverge from the remaining angiosperms be
fore Ceratophyllum + water lilies. Rooted species trees inferred from dupli
cate gene networks by minimizing gene duplications and losses are highly co
ngruent with the gene subtrees and with the results of recent analyses of o
ther genes, even when Ceratophyllum is included. More attention must be pai
d to the methods for obtaining rooted species trees from data sets that inc
lude duplicate genes, especially if we are to fully implement the search fo
r species trees that simultaneously minimize the multiple possible causes o
f conflict among gene trees.