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834 POACEAE/ARUNDINARIA<br />

Arthraxon hispidus (Thunb.) Makino, (hairy, bristly), SMALL CARP GRASS, JOINT-HEAD. Low annual;<br />

culms <strong>to</strong> 80(–100) cm long (rarely longer), creeping and rooting at lower nodes, glabrous;<br />

leaf blades lanceolate <strong>to</strong> ovate, 4–15(–20) mm wide, cordate-clasping; leaf sheaths hispid; ligule<br />

ciliate, ca. 1–3 mm long; racemes ca. 2–7 cm long, spike-like, usually 2–11(–15) in a digitate cluster;<br />

spikelets sessile, perfect, solitary (or in pairs—if pedicellate spikelet present, this sterile or<br />

reduced <strong>to</strong> a pedicel); disarticulation so that sessile spikelet falls with associated pedicel (if<br />

present) and section <strong>of</strong> <strong>the</strong> inflorescence branch; sessile spikelets 2–5 mm long, with 2 florets;<br />

glumes 2, equal, coarser in texture than membranous lemmas; lower floret sterile, awnless; upper<br />

(fertile) lemma awnless or with an awn <strong>to</strong> 7(–10) mm long, <strong>the</strong> awn attached anywhere<br />

from near <strong>the</strong> midpoint <strong>to</strong> <strong>the</strong> base <strong>of</strong> <strong>the</strong> midvein; palea absent. Moist areas, ditches, open<br />

places; Cass Co. (Brown & Schultz 1991—<strong>the</strong> first collection reported for TX); e U.S. from NY s <strong>to</strong><br />

FL w <strong>to</strong> KS and TX; first collected in <strong>the</strong> U.S. in PA in 1877 (Kiger 1971). Fall. Native <strong>of</strong> Asia. [A.<br />

ciliaris P. Beauv., A. crypta<strong>the</strong>rus var. ciliaris (P. Beauv.) Koidz., A. hispidus subsp. ciliaris (P.<br />

Beauv.) Masam. & Yanagih.] According <strong>to</strong> Thieret (2003c), <strong>plants</strong> in <strong>the</strong> U.S. belong <strong>to</strong> var.<br />

hispidus, “<strong>the</strong> most widespread and variable <strong>of</strong> <strong>the</strong> four varieties.” This species is used medicinally<br />

in China, and it is <strong>the</strong> source <strong>of</strong> a yellow dye (Mabberley 1997). I<br />

ARUNDINARIA Michx. CANE<br />

AA C3 n temperate genus <strong>of</strong> ca. 50 species (Tucker 1988; Watson & Dallwitz 1992) <strong>of</strong> BAMBOOS<br />

ranging from n India <strong>to</strong> China and Japan, with only 1 species native <strong>to</strong> <strong>the</strong> New World—A.<br />

gigantea, endemic <strong>to</strong> <strong>the</strong> se U.S. However, <strong>the</strong>re is considerable disagreement over which Asian<br />

species should be included (Clark ined.), and <strong>the</strong>refore uncertainty in <strong>the</strong> number <strong>of</strong> species in<br />

<strong>the</strong> genus. Some species are used for fishing rods, umbrella shafts, and furniture, while o<strong>the</strong>rs<br />

are cultivated as ornamentals or used in bonsai (Watson & Dallwitz 1992). (Latin: arundo, a<br />

reed) (subfamily Bambusoideae, tribe Bambuseae)<br />

REFERENCES: McClure 1963, 1973; Haubrich 1980; Tucker 1988; Platt & Brantley 1997; Judziewicz<br />

et al. 1999; Grass Phylogeny Working Group 2000; Clark ined.<br />

Arundinaria gigantea (Walter) Muhl., (gigantic), GIANT CANE, SOUTHERN CANE, SWITCH CANE,<br />

BAMBOO. Much-branched, woody, evergreen perennial (0.5–)2–5(–8) m or more tall from a usually<br />

solid rhizome; culms rounded, <strong>to</strong> ca. 3 cm in diam., <strong>the</strong> upper nodes <strong>of</strong>ten puberulent;<br />

branches 3–6 per node; leaves variable, <strong>the</strong> lower <strong>of</strong>ten reduced; ligule a firm membrane 1.5 mm<br />

or less long; leaf blades abruptly narrowed <strong>to</strong> a joint-like connection <strong>to</strong> <strong>the</strong> leaf sheaths; upper<br />

leaf blades usually 15–25(–30) cm long, 2–4(–5.5) cm wide; inflorescences racemose or narrowly<br />

paniculate; spikelets 1–few, large, 4–7(–8) cm long, ca. 8 mm broad, with 6–12(–13) florets,<br />

greenish or brownish; lemmas (10–)15–25 mm long, usually with pubescence. Moist woods or<br />

low areas, can form dense, nearly monocultural stands known as canebrakes (previously sometimes<br />

spelled canebreaks); Pineywoods and Post Oak Savannah w <strong>to</strong> Robertson Co. (Turner et al.<br />

2003) and <strong>to</strong> at l<strong>east</strong> Lamar Co. (BRIT) in Red River drainage; Turner et al. (2003) also mapped a<br />

Grayson Co. location even fur<strong>the</strong>r w in Red River drainage; also n Gulf Prairies and Marshes;<br />

Hatch (2002) also cited <strong>the</strong> Edwards Plateau and Trans-Pecos; e U.S. from OH <strong>to</strong> FL w <strong>to</strong> KS and<br />

TX. Mostly Apr–May. This is <strong>the</strong> only native bamboo species in TX. It was used by Native<br />

Americans and o<strong>the</strong>rs for such things as construction material, baskets, mats, pipestems, weapons,<br />

fishing poles, and food (cooked young shoots and fruits) (Platt & Brantley 1997;<br />

Yatskievych 1999). According <strong>to</strong> Yatskievych (1999), “The species is propagated mostly by rhizome<br />

fragments that are transported by water. … Reports <strong>of</strong> <strong>the</strong> species’ life cycle are conflicting,<br />

ranging from an annual flowering cycle <strong>to</strong> flowering every 30–40 years, and from mortality <strong>of</strong><br />

<strong>the</strong> plant following flowering, <strong>to</strong> none <strong>of</strong> <strong>the</strong> die-<strong>of</strong>f that is typical <strong>of</strong> most bamboos. Plants cultivated<br />

in St. Louis County [MO] flowered annually from 1993 <strong>to</strong> 1996 with no evidence <strong>of</strong> decline<br />

<strong>of</strong> existing stems.” Gould (1975b), however, reported that <strong>the</strong> <strong>plants</strong> flower only at intervals<br />

<strong>of</strong> 4–6 years. Canebrakes were once extensive in alluvial floodplains, were a dominant

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