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1042 POACEAE/SACCHARUM<br />

<strong>of</strong> each spikelet with a long awn (awn absent in S. <strong>of</strong>ficinarum); palea <strong>of</strong> fertile floret ca. 1/2 as<br />

long as lemma; palea <strong>of</strong> sterile floret absent; stamens usually 2 (3 in S. <strong>of</strong>ficinarum).<br />

AThe genus, as treated here including Erianthus, comprises 35–40 species (Webster & Shaw<br />

1995; Mabberley 1997; Webster 2003) <strong>of</strong> tropical and warm areas <strong>of</strong> <strong>the</strong> world. The center <strong>of</strong> diversity,<br />

with ca. 25 species, is tropical Asia (Webster & Shaw 1995). Like all members <strong>of</strong> <strong>the</strong><br />

Andropogoneae, Saccharum is characterized by C4 pho<strong>to</strong>syn<strong>the</strong>sis (Kellogg 2000a). The traditional<br />

segregation <strong>of</strong> awned species as Erianthus and awnless species as Saccharum has been<br />

described as “wholly artificial” (Clay<strong>to</strong>n & Renvoize 1986). Some authorities (e.g., Daniels &<br />

Roach 1987; Whalen 1991) disagree, and <strong>the</strong>y treat Saccharum more narrowly, including only<br />

SUGARCANE and its immediate relatives (only 5 species), with <strong>the</strong> rest <strong>of</strong> <strong>the</strong> species segregated<br />

in<strong>to</strong> Erianthus. However, Burner and Webster (1994) successfully obtained hybrids between<br />

Erianthus species and SUGARCANE, and Burner et al. (1997) found North American Erianthus <strong>to</strong><br />

be genetically similar <strong>to</strong> SUGARCANE cultivars. None<strong>the</strong>less, recent molecular research (Dillon<br />

et al. 2001) raises <strong>the</strong> possibility that Saccharum <strong>of</strong>ficinarum (SUGARCANE) is derived from<br />

within Sorghum, while Erianthus appears more closely related <strong>to</strong> Zea; such results argue for <strong>the</strong><br />

separate recognition <strong>of</strong> Erianthus. Likewise, Nair et al. (1999) found “considerable divergence”<br />

between Erianthus and Saccharum. Until such issues are resolved, we are following most recent<br />

authorities (e.g., Hatch 2002; Webster 2003) in treating Saccharum broadly, <strong>to</strong> include<br />

Erianthus. Saccharum is related <strong>to</strong> Eulalia, Imperata, and Miscanthus, and it also will hybridize<br />

with Sorghum (Gupta et al. 1978). Webster and Shaw (1995) indicated that <strong>the</strong> “single most<br />

reliable character for distinguishing among <strong>the</strong> [North American] taxa is <strong>the</strong> length <strong>of</strong> <strong>the</strong> callus<br />

hairs relative <strong>to</strong> spikelet length.” The long callus hairs may aid in dispersal by wind (Webster<br />

& Shaw 1995). The economically most important member <strong>of</strong> <strong>the</strong> genus is S. <strong>of</strong>ficinarum L.<br />

(SUGARCANE), which is <strong>the</strong> source <strong>of</strong> ca. 1/2 <strong>of</strong> <strong>the</strong> world’s sugar. � Saccharum spontaneum L.,<br />

WILD SUGARCANE, known in <strong>the</strong> U.S. from HI and PR, is a federal noxious weed (Kartesz 1999;<br />

USDA Natural Resources Conservation Service 2002). The following treatment draws heavily<br />

on Webster and Shaw (1995). (Latin: saccharum, sugar, referring <strong>to</strong> <strong>the</strong> sweet sap) (subfamily<br />

Panicoideae, tribe Andropogoneae)<br />

REFERENCES: Mukherjee 1958; Daniels & Roach 1987; Reveal et al. 1989; Whalen 1991; Gandhi &<br />

Dut<strong>to</strong>n 1993; Burner & Webster 1994; Webster & Shaw 1995; Nair et al. 1999; Weakley 2000;<br />

Webster 2003.<br />

1. Lemma <strong>of</strong> fertile (= upper) floret without an awn; an<strong>the</strong>rs 3 per floret; introduced cultivated<br />

species rarely if ever escaping in East TX ____________________________________________ S. <strong>of</strong>ficinarum<br />

1. Lemma <strong>of</strong> fertile floret with a conspicuous awn; an<strong>the</strong>rs 2 per floret; native species widespread<br />

in East TX.<br />

2. Awn <strong>of</strong> lemma <strong>of</strong> fertile floret spiraled at base (<strong>the</strong> spiral is easily visible <strong>to</strong> <strong>the</strong> naked eye).<br />

3. Callus hairs (= conspicuous whorl <strong>of</strong> hairs attached directly below spikelet) equal <strong>to</strong> or<br />

shorter than spikelet, 3–6.5 mm long, white <strong>to</strong> straw-colored or brownish; peduncle (=<br />

stalk <strong>of</strong> inflorescence) glabrous or with sparse pubescence just below inflorescence _____ S. brevibarbe<br />

3. Callus hairs longer than spikelet, ca. 9–14 mm long, silvery or purplish tinged; peduncle<br />

with conspicuous, appressed, long pubescence just below inflorescence ___________ S. alopecuroides<br />

2. Awn <strong>of</strong> lemma <strong>of</strong> fertile floret not spiraled at base.<br />

4. Callus hairs longer than spikelet, (7–)15–20(–25) mm long; lemma <strong>of</strong> fertile floret with a<br />

single vein; peduncle with conspicuous, appressed, long pubescence just below inflorescence;<br />

leaf blades with sparse long pubescence on upper surface ____________________ S. giganteum<br />

4. Callus hairs equal <strong>to</strong> or shorter than spikelet, 0–6.5 mm long or absent; lemma <strong>of</strong> fertile<br />

floret with 3 veins; peduncle glabrous or with sparse pubescence; leaf blades glabrous on<br />

upper surface.<br />

5. Callus glabrous or with hairs 2 mm long or less; main branches <strong>of</strong> inflorescence glabrous,<br />

appressed, <strong>the</strong> inflorescence thus only 1–3 cm wide ________________________ S. baldwinii

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