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keys to the vascular plants of east texas - Botanical Research ...

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1136 TYPHACEAE<br />

bract length); flowers sessile or subsessile (pedicel 3 mm or less long), with a faint fetid aroma;<br />

sepals abruptly recurved basally and � held against scape, green or streaked with purple, (15–)<br />

20–30(–35) mm long; petals erect, dark purple <strong>to</strong> yellowish green or yellow, lanceolate <strong>to</strong> oblanceolate<br />

or ovate, distinctly clawed, 18–40(–50) mm long; an<strong>the</strong>rs 5–16 mm long; gynoecium ca.<br />

reaching bases <strong>of</strong> an<strong>the</strong>rs; ovary 6-angled or -winged; fruit 6-angled <strong>to</strong> nearly winged. Alluvial<br />

banks in rich mesic hardwood forests, typically neutral soils that are moist due <strong>to</strong> seepage; Rusk<br />

(BRIT), Nacogdoches (Freeman 1970; Nixon et al. 1970; TOES 1993), and Shelby (Singhurst et al.<br />

2002b) cos. in <strong>the</strong> Pineywoods; ec U.S. from OH and AL w <strong>to</strong> WI and TX. Mar–May. First reported<br />

for TX by Nixon et al. (1970). (TOES 1993: IV) �/305<br />

Trillium viridescens Nutt., (greenish), LONG-PETALED TRILLIUM, OZARK GREEN TRILLIUM, OZARK<br />

TRILLIUM. Plant 20–50(–59) cm tall; leaf-like bracts ovate-elliptic <strong>to</strong> broadly ovate or elliptic, 9–<br />

14(–15) cm long, rounded <strong>to</strong> acute (acuminate <strong>to</strong> <strong>the</strong> n <strong>of</strong> TX), sessile, not mottled or only obscurely<br />

so, sometimes (not usually) with s<strong>to</strong>mata on upper (= adaxial) leaf epidermis at <strong>the</strong><br />

apex; flowers sessile, with musty-spicy odor similar (according <strong>to</strong> some) <strong>to</strong> rotting apples or<br />

spoiled fruit; sepals spreading, green or with purple tinge, 3.5–5.4(–6.5) cm long; petals erect or<br />

nearly so, variable in color, greenish purple or greenish, with a purple claw, sometimes purple or<br />

yellowish green throughout, linear-spatulate <strong>to</strong> narrowly spatulate, 4.3–8(–8.5) cm long; an<strong>the</strong>rs<br />

13–20 mm long; ovary 6-angled; fruit 6-ridged, rarely winged. Rich woods, wooded slopes,<br />

sandy or clay soils; Nacogdoches (BAYLU), Harrison, Marion, Red River (Freeman 1970), Bowie,<br />

and Sabine (Singhurst et al. 2002b) cos. in <strong>the</strong> n Pineywoods and Red River drainage; AR, KS,<br />

MO, OK, and TX. Apr–early May. These TX populations are <strong>the</strong> s extreme <strong>of</strong> <strong>the</strong> range <strong>of</strong> <strong>the</strong><br />

species (Freeman 1970). While treating it as a separate species, Churchill (1986b) suggested that<br />

T. viridescens might be better treated as a subspecies <strong>of</strong> T. viride L.C. Beck. Yatskievych (1999)<br />

also discussed <strong>the</strong> similarities between T. viridescens and T. viride; he indicated <strong>the</strong> most reliable<br />

morphological character distinguishing <strong>the</strong>m is <strong>the</strong> distribution <strong>of</strong> s<strong>to</strong>mata on <strong>the</strong> bracts—<br />

evenly distributed over <strong>the</strong> abaxial leaf surface in T. viride and lacking or only at <strong>the</strong> leaf tip in<br />

T. viridescens; he suggested that ambiguities in o<strong>the</strong>r characters lend weight <strong>to</strong> <strong>the</strong> opinions <strong>of</strong><br />

those botanists who would prefer <strong>to</strong> treat <strong>the</strong> two taxa as varieties or subspecies <strong>of</strong> T. viride or<br />

simply not recognize T. viridescens as distinct. Freeman (1975) raised <strong>the</strong> possibility <strong>of</strong> introgression<br />

between T. viridescens and T. gracile. This species is cited by Case (2002) as being <strong>of</strong><br />

conservation concern. �/305<br />

TYPHACEAE Juss.<br />

CAT-TAIL FAMILY<br />

AA very small (8–13 species—Smith 2000), cosmopolitan family <strong>of</strong> wind-pollinated and<br />

wind-dispersed <strong>plants</strong> represented by a single genus. Typha and Sparganium (Sparganiaceae)<br />

are quite similar, and it has been suggested that <strong>the</strong> two are best united in<strong>to</strong> a single family<br />

(Thorne 1993c; Mabberley 1997; Kubitzki 1998b; Judd et al. 1999). Thieret and Luken (1996)<br />

quoted Müller-Doblies (1970) as saying that <strong>the</strong> “… obvious differences may be explained <strong>to</strong> a<br />

large extend [sic] by an adaptation <strong>of</strong> Typha <strong>to</strong> anemochory [wind dispersal].” However, <strong>the</strong> most<br />

recent monographers <strong>of</strong> Sparganium (Cook & Nicholls 1986, 1987) noted that <strong>the</strong> two groups<br />

are clearly distinct morphologically and have been so since at l<strong>east</strong> <strong>the</strong> Oligocene (ca. 38 <strong>to</strong> 23<br />

million years ago). They concluded that <strong>the</strong>re is no purpose in uniting <strong>the</strong> two families, and significant<br />

disadvantages—e.g., nomenclatural instability. (subclass Commelinidae–Cronquist; order<br />

Poales—APG II)<br />

FAMILY RECOGNITION IN THE FIELD: large perennial herbs with elongate, sublinear, spongy, 2ranked<br />

leaves and dense, felty, brown, cylindrical inflorescences divided in<strong>to</strong> a male portion<br />

above and a female portion below; typically found in wet places.

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