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866 POACEAE/CHLORIS<br />

divergent; spikelets flat, 4–7(–9) mm wide, usually with 4–7 florets. Moist forests, swamps, and<br />

prairie openings, sandy soils; Pineywoods and Post Oak Savannah, also Dallas Co. (Turner et al.<br />

2003) <strong>to</strong> <strong>the</strong> w; also n Gulf Prairies and Marshes; se U.S. from VA s <strong>to</strong> FL w <strong>to</strong> OK and TX. Jun–<br />

Nov. [C. laxum subsp. sessiliflorum (Poir.) L.G. Clark, C. laxum var. sessiliflorum (Poir.) Wipff &<br />

S.D. Jones, Uniola sessiliflora Poir.] This taxon has been variously treated taxonomically. It has<br />

been recognized as a separate species (e.g., Kartesz 1999), as a subspecies <strong>of</strong> C. laxum (e.g., Clark<br />

1990; Yatskievych 1999), as a variety <strong>of</strong> C. laxum (e.g., Wipff & Jones 1994 [1995]; Diggs et al.<br />

1999), or as part <strong>of</strong> an undivided C. laxum (e.g., Hatch 2002). Clark (1990) indicated <strong>the</strong>re is significant<br />

overlap between <strong>the</strong> two taxa in a number <strong>of</strong> morphological characters and that <strong>the</strong>y<br />

are almost completely sympatric; he concluded that <strong>the</strong>y are not worthy <strong>of</strong> recognition as species.<br />

Recently, Sánchez-Ken and Clark (2003) treated <strong>the</strong> two at <strong>the</strong> species level and gave a<br />

number <strong>of</strong> morphological characters (used in <strong>the</strong> key above) by which <strong>to</strong> distinguish <strong>the</strong>m.<br />

Even though sympatric, <strong>the</strong> differences between <strong>the</strong>m seem <strong>to</strong> be maintained. Additionally,<br />

Sánchez-Ken and Clark (2003) noted that, while growing in similar habitats, C. sessiliflorum<br />

extends “fur<strong>the</strong>r in<strong>to</strong> sphagnous stream heads, pine flatwoods, and pine savannahs.” Because <strong>of</strong><br />

<strong>the</strong>se morphological and ecological differences, we are following Sánchez-Ken and Clark (2003)<br />

in treating C. sessiliflorum as a separate species.<br />

CHLORIS Sw. WINDMILL GRASS<br />

Annuals or perennials; leaf sheaths strongly compressed and sharply keeled; ligule a ciliate membrane;<br />

branches <strong>of</strong> inflorescence digitately or subdigitately arranged at tip <strong>of</strong> culm (apparently in<br />

1 whorl) or else in several whorls; spikelets in 2 rows along 1 side <strong>of</strong> <strong>the</strong> branch axes, with 1(–2)<br />

perfect floret at base and 1 or more reduced ones above, laterally compressed, disarticulating<br />

above <strong>the</strong> glumes; glumes shorter than fertile floret; lemma <strong>of</strong> perfect floret usually awned, marginally<br />

<strong>of</strong>ten variously and sometimes conspicuously pubescent; reduced florets without paleas.<br />

AA C4 genus <strong>of</strong> 55–60 species (Barkworth 2003b) <strong>of</strong> tropical and warm areas <strong>of</strong> <strong>the</strong> world<br />

(most abundant in <strong>the</strong> s hemisphere). The genus includes some fodder and pasture grasses, as<br />

well as a number <strong>of</strong> significant weeds (Watson & Dallwitz 1992). Recent molecular studies<br />

(Hilu & Alice 2000, 2001) raise questions about <strong>the</strong> monophyly <strong>of</strong> Chloris as traditionally delimited.<br />

Enteropogon, UMBRELLA GRASS, here treated as a separate genus following Barkworth<br />

(2003b), is sometimes included in Chloris (e.g., Correll & Johns<strong>to</strong>n 1970; Gould 1975b; Hatch et<br />

al. 1990). The most reliable character in separating <strong>the</strong> two genera is compression <strong>of</strong> <strong>the</strong> spikelets:<br />

dorsally compressed in Enteropogon versus laterally compressed in Chloris (Jacobs &<br />

Highet 1988). Molecular data link Chloris, Cynodon, Enteropogon, and Eustachys but do not<br />

support combining <strong>the</strong> genera (Hilu & Alice 2000). Intergeneric hybrids <strong>of</strong> Chloris with<br />

Cynodon are known (Watson & Dallwitz 1992). The following treatment draws heavily on<br />

Gould (1975b). (Named for Chloris, Greek mo<strong>the</strong>r <strong>of</strong> Nes<strong>to</strong>r, goddess <strong>of</strong> flowers) (subfamily<br />

Chloridoideae, tribe Cynodonteae)<br />

REFERENCES: Nash 1898; Clay<strong>to</strong>n 1967a, 1982; Lazarides 1972; Anderson 1974; Gould 1975b;<br />

Varadarajan & Gilmartin 1983a, 1983b; Jacobs & Highet 1988; Hilu & Alice 2000, 2001;<br />

Barkworth 2003b.<br />

1. Branches <strong>of</strong> inflorescence in 2–5 whorls along a main axis usually 20 mm or more long; reduced<br />

(neuter or staminate) floret 1 per spikelet, truncate ____________________________________ C. verticillata<br />

1. Branches <strong>of</strong> inflorescence usually in only 1 whorl, or appearing so (if in more than 1 whorl, <strong>the</strong>n<br />

<strong>the</strong> whorls crowded along an axis less than 20 mm long); reduced floret(s) 1–4 per spikelet,<br />

truncate or not so.<br />

2. Reduced floret 1 per spikelet; including species widespread and common in East TX.<br />

3. Inflorescence branches bearing spikelets <strong>to</strong> very base; lowest spikelets <strong>of</strong> branch typically<br />

less than 3 mm apart.

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