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1130 TRILLIACEAE<br />

as treated here following Zomlefer (1997b), is a monophyletic group, only “distantly related” <strong>to</strong><br />

o<strong>the</strong>r groups with which it has been affiliated in <strong>the</strong> past (Zomlefer 1997b). The T<strong>of</strong>ieldiaceae<br />

has sometimes been put in its own order, <strong>the</strong> T<strong>of</strong>ieldiales (Reveal & Zomlefer 1998; Zomlefer<br />

1999), but recent molecular analyses (e.g., Chase et al. 2000) and <strong>the</strong> Angiosperm Phylogeny<br />

Group (APG II 2003) place <strong>the</strong> family in <strong>the</strong> Alismatales. It is thus in a clade near <strong>the</strong> base <strong>of</strong> <strong>the</strong><br />

monocots, most closely related <strong>to</strong> a group <strong>of</strong> families including <strong>the</strong> Alismataceae and Araceae<br />

(Fuse & Tamura 2000). For a detailed discussion <strong>of</strong> <strong>the</strong> groups formerly treated as Liliaceae in<br />

<strong>the</strong> broad sense, see <strong>the</strong> family synopsis <strong>of</strong> <strong>the</strong> Liliaceae (here treated in a restricted sense) on<br />

page 726. Family name from T<strong>of</strong>ieldia, a North American and Eurasian genus <strong>of</strong> 7 or 8 (Packer<br />

2002a) species, <strong>of</strong>ten interpreted <strong>to</strong> include species now segregated as Triantha (see e.g., Tamura<br />

1998c). (Named for Thomas T<strong>of</strong>ield, 1730–1779, British botanist) (subclass Liliidae—Cronquist;<br />

order Alismatales—APG II)<br />

FAMILY RECOGNITION IN THE FIELD: <strong>the</strong> only East Texas species is a subscapose perennial herb<br />

from rhizomes, with small, creamy white <strong>to</strong> white flowers in a racemose inflorescence, <strong>the</strong><br />

scape minutely glandular pubescent below <strong>the</strong> inflorescence, and 3 basally fused styles.<br />

REFERENCES: Zomlefer 1997a, 1997b, 1999; Reveal & Zomlefer 1998; Tamura 1998c; Fuse &<br />

Tamura 2000.<br />

TRIANTHA (Nutt.) Baker FALSE ASPHODEL<br />

AA genus <strong>of</strong> 4 species <strong>of</strong> North America and Japan (Packer 2002b). It was previously placed<br />

in a heterogeneous T<strong>of</strong>ieldia (e.g., Correll & Johns<strong>to</strong>n 1970; Hatch et al. 1990), but recent studies<br />

(Cruden 1991; Packer 1993, 2002b) support its recognition as a separate genus. (Greek: tri-,<br />

three-, and anthos, flower, in reference <strong>to</strong> <strong>the</strong> flowers aggregated in threes)<br />

REFERENCES: Cruden 1991; Packer 1993, 2002b.<br />

Triantha racemosa (Walter) Small, (with a raceme type inflorescence), STICKY TOFIELDIA,<br />

COASTAL FALSE ASPHODEL. Perennial subscapose herb from rhizomes; stem 30–70 cm tall, minutely<br />

glandular pubescent below inflorescence; leaves mostly at base <strong>of</strong> plant but one usually<br />

below middle <strong>of</strong> stem; basal leaves 2-ranked, linear, grass-like, erect, 30–40(–50) cm long, 3–6<br />

mm wide; leaf <strong>of</strong> stem small, bract-like; inflorescence racemose, 5–15(–22) cm long, <strong>the</strong> flowers<br />

clusered 2–3(–7) <strong>to</strong>ge<strong>the</strong>r at <strong>the</strong> nodes in lower part <strong>of</strong> inflorescence, sometimes single above,<br />

with terminal flowers opening first; pedicels pubescent, each bearing 3 minute connate bracts<br />

just below <strong>the</strong> flower; flowers perfect; perianth segments separate, spreading, oblanceolate <strong>to</strong><br />

oblong, creamy white or white, drying orangish, 3-nerved, obtuse, (2.5–)3–5 mm long, persistent<br />

in fruit; stamens 6; ovary superior, 3-locular; styles 3, connate basally in<strong>to</strong> column 1/4–2/3 <strong>the</strong>ir<br />

length; capsule equal <strong>to</strong> or slightly shorter than and � enclosed by <strong>the</strong> perianth, ca. 3–5 mm<br />

long, tipped by <strong>the</strong> divergent, enlarged, persistent styles; seeds numerous, ca. 2 mm long (body<br />

ca. 1 mm), usually appendaged at both ends with membranous white tails each ca. 1/2 as long<br />

as <strong>the</strong> body or shorter (one sometimes much shorter or absent) (<strong>the</strong>se appendages are presumably<br />

for wind dispersal—Rendle 1930). Wet sandy soils <strong>of</strong> pine savannahs, bogs, seepage slopes;<br />

Tyler (BRIT, ASTC) and Jefferson (Turner et al. 2003) cos. in <strong>the</strong> Pineywoods; se U.S. from DE s <strong>to</strong><br />

FL w <strong>to</strong> TX. Jun–Sep. [Melanthium racemosum Walt., T<strong>of</strong>ieldia racemosa (Walt.) Brit<strong>to</strong>n, Sterns,<br />

& Poggenb.] While not <strong>of</strong>ficially designated as such (e.g., TOES 1993; Carr 2002d; Poole et al.<br />

2002), given its limited distribution in <strong>the</strong> state, we consider this species <strong>to</strong> be <strong>of</strong> conservation<br />

concern in TX. � m/305<br />

TRILLIACEAE Lindl.<br />

WAKE-ROBIN FAMILY<br />

AA small n hemisphere family <strong>of</strong> probably 4–6 genera and ca. 50–71 species <strong>of</strong> woodland<br />

herbs, occurring in subarctic <strong>to</strong> subtropical areas (Zomlefer 1996; Tamura 1998d; Farmer &

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