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1034 POACEAE/PIPTOCHAETIUM<br />

sometimes weedy colonies covering large areas (<strong>of</strong>ten excluding o<strong>the</strong>r vegetation); nearly<br />

throughout East TX w <strong>to</strong> Cross Timbers and Prairies (Borowski et al. 1996); se U.S. from MD s <strong>to</strong><br />

FL w <strong>to</strong> AR and TX, also OR. We have seen only one flowering collection from East TX. Native<br />

<strong>of</strong> China. [Bambusa aurea Hort] Like many bamboos, Phyllostachys species generally flower<br />

synchronously only after intervals <strong>of</strong> many years. In some species, <strong>the</strong>se flowering cycles are up<br />

<strong>to</strong> 120 years in length, apparently based on an internal physiological calendar (Janzen 1976;<br />

Judd et al. 1999). Janzen (1976) reported <strong>the</strong> intermast period (= time period between successive<br />

fruit/seed production events) in P. aurea <strong>to</strong> be “28–29 (2� 14–15)” years, based on specimens cultivated<br />

in Europe. However, he also indicated that cultivation and o<strong>the</strong>r fac<strong>to</strong>rs can affect <strong>the</strong><br />

flowering interval. Texas <strong>plants</strong> may thus have lost synchrony and not display such a flowering<br />

pattern. It has been hypo<strong>the</strong>sized that such long intervals between flowering evolved as a<br />

mechanism <strong>to</strong> escape seed predation (Janzen 1976). Large amounts <strong>of</strong> seed produced at intervals<br />

would hinder <strong>the</strong> buildup <strong>of</strong> populations <strong>of</strong> seed preda<strong>to</strong>rs and lead <strong>to</strong> satiation <strong>of</strong> any<br />

seed preda<strong>to</strong>rs present—only so much can be eaten at one time and thus many seeds would escape<br />

predation. This species was introduced <strong>to</strong> <strong>the</strong> U.S. prior <strong>to</strong> 1870 (Rehder 1927) as an ornamental,<br />

for barrier planting, and for erosion control and soil stabilization (Borowski et al. 1996).<br />

The young shoots are reported <strong>to</strong> be “very palatable” (Barkworth & Clark ined.) and <strong>the</strong> mature<br />

culms are sometimes used as fishing poles. I<br />

A variety <strong>of</strong> o<strong>the</strong>r exotic bamboos, including Bambusa species (e.g., B. multiplex (Lour.) Raeusch.<br />

ex Schult. & Schult. f., HEDGE BAMBOO) and additional species <strong>of</strong> Phyllostachys (e.g., P. nigra<br />

(Lodd.) Munro, BLACK BAMBOO, with black culms) are cultivated in East TX. Our only native<br />

bamboo, Arundinaria gigantea (GIANT CANE), occurs in moist woods and low areas from <strong>the</strong><br />

Pineywoods and n Gulf Prairies and Marshes w <strong>to</strong> at l<strong>east</strong> Lamar Co. (BRIT) in <strong>the</strong> Red River<br />

drainage.<br />

PIPTOCHAETIUM J. Presl SPEAR GRASS<br />

AA New World mainly temperate C3 genus <strong>of</strong> 36 species (Cialdella & Giussani 2002), ranging<br />

from <strong>the</strong> U.S. <strong>to</strong> Argentina, with most in South America, and particularly abundant in Argentina<br />

(Barkworth ined.). Migration between North and South America is thought <strong>to</strong> have occurred<br />

during <strong>the</strong> late Tertiary Period, in association with <strong>the</strong> movement <strong>of</strong> herbivorous mammals<br />

(Williams 1975; Thomasson 1980). Recent studies (Cialdella & Giussani 2002) suggest <strong>the</strong><br />

genus is monophyletic. Pip<strong>to</strong>chaetium species have sometimes been put in<strong>to</strong> Stipa (e.g., Gould<br />

1975b) and also resemble species <strong>of</strong> Nassella. However, according <strong>to</strong> Clay<strong>to</strong>n and Renvoize<br />

(1986), while <strong>the</strong> genus can imitate Stipa and Nassella, “but is readily distinguished by its<br />

grooved palea.” Also, Pip<strong>to</strong>chaetium can be distinguished unambiguously from Nassella (with<br />

strongly overlapping lemma margins) by its involute, non-overlapping lemma margins<br />

(Barkworth 1990, ined.) and palea protruding from <strong>the</strong> lemma (versus not protruding in<br />

Nassella) (Cialdella & Giussani 2002). (Greek: pip<strong>to</strong>, <strong>to</strong> fall, and chaite, long hair, mane, or<br />

bristle, in reference <strong>to</strong> <strong>the</strong> deciduous awns <strong>of</strong> <strong>the</strong> type species) (subfamily Pooideae, tribe Stipeae)<br />

REFERENCES: Hitchcock 1925; Parodi 1944; Thomasson 1978, 1980; Clay<strong>to</strong>n 1983; Barkworth<br />

1990, 1993, ined.; Tucker 1990; Cialdella & Arriaga 1998; Cialdella & Giussani 2002.<br />

Pip<strong>to</strong>chaetium avenaceum (L.) Parodi, (resembling Avena—OATS), BLACK-SEED SPEAR GRASS,<br />

BLACK-SEED NEEDLE GRASS, BLACK OAT GRASS, OATS NEEDLE GRASS, EASTERN NEEDLE GRASS. Perennial,<br />

tufted, (35–)50–80(–100) cm tall; ligule membranous, (0.4–)1.5–4.5 mm long; leaf blades ca.<br />

0.8–1.5(–3) mm wide; panicles with few spikelets; spikelets 1-flowered, disarticulating above <strong>the</strong><br />

glumes; glumes acuminate, (9–)10–12(–15) mm long, � equal; lemma 8–12 mm long (including<br />

callus), indurate, dark (brown or purplish) at maturity, <strong>the</strong> margins involute, not overlapping<br />

(rounded portions abutting), with a very long (3.5–10 cm), geniculate, twisted awn; lemma apex<br />

without a white neck or crown (as in some Nassella species) but with a fringe <strong>of</strong> brown hairs

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