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

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950 POACEAE/FESTUCA<br />

2–10 florets, glabrous or nearly so; disarticulation above glumes and between florets; glumes 2,<br />

unequal, <strong>the</strong> upper one longer, usually slightly shorter than lower lemma; lemmas usually<br />

rounded on back, not <strong>to</strong>o<strong>the</strong>d at apex, awnless or with a short awn; stamens 3.<br />

AA C3 genus <strong>of</strong> ca. 400–450 species (Mabberley 1997; Darbyshire & Pavlick ined.) <strong>of</strong> temperate,<br />

alpine, and polar areas <strong>of</strong> all continents except Antarctica, and in tropical mountains. Some<br />

are important as pasture and lawn grasses, while o<strong>the</strong>rs are considered significant weeds (Watson<br />

& Dallwitz 1992). Vulpia (SIXWEEKS GRASS, ANNUAL FESCUE), treated here as a separate genus,<br />

has in <strong>the</strong> past sometimes been included in Festuca. A number <strong>of</strong> workers (e.g., Bulinska-<br />

Radomska & Lester 1988; Pasakinskiene et al. 1998) have noted similarities between <strong>the</strong> genera<br />

Festuca, Lolium, and Vulpia, and it now seems clear that Lolium is most closely related <strong>to</strong> some<br />

species <strong>of</strong> Festuca (Gaut et al. 2000). In addition, intergeneric hybrids between Lolium and<br />

Festuca are known (Terrell 1966; Watson & Dallwitz 1992). Darbyshire (1993) suggested that<br />

Festuca subgenus Schedonorus, <strong>the</strong> broad-leaved fescues (including F. arundinacea and F.<br />

pratensis), be shifted <strong>to</strong> Lolium based on a number <strong>of</strong> types <strong>of</strong> experimental evidence including<br />

hybridization. Tucker (1996) followed that classification. More recently (Darbyshire ined.) has<br />

recognized subgenus Schedonorus at <strong>the</strong> generic level and considers it <strong>to</strong> comprise 3 species<br />

native <strong>to</strong> Europe and temperate Asia. However, o<strong>the</strong>r recent studies (e.g., Aiken et al. 1997;<br />

Charmet et al. 1997; Gaut et al. 2000) suggest <strong>the</strong> situation is more complex. In fact, some molecular<br />

data (e.g., Charmet et al. 1997) indicate that Lolium, Vulpia, and possibly Dactylis are<br />

derived from within Festuca and even raise <strong>the</strong> possibility that Festuca might be polyphyletic.<br />

A more recent study (Torrecilla & Catalán 2000) suggests that only Festuca in <strong>the</strong> broad sense<br />

(including Lolium and Vulpia) is monophyletic. It is thus not yet clear what is <strong>the</strong> best arrangement<br />

<strong>of</strong> <strong>the</strong>se genera (i.e., one large genus, a genus with subgenera, a number <strong>of</strong> smaller genera,<br />

etc.). We are <strong>the</strong>refore following such recent authors as Yatskievych (1999) in retaining subgenus<br />

Schedonorus in Festuca, at l<strong>east</strong> for <strong>the</strong> present. As more information becomes available, a<br />

reassessment <strong>of</strong> generic boundaries may be necessary. Clay<strong>to</strong>n and Renvoize (1986), while recognizing<br />

<strong>the</strong> similarities between F. arundinacea (and related species) and Lolium, said, “Never<strong>the</strong>less<br />

<strong>the</strong> two genera are so easily distinguished that it seems unrealistic <strong>to</strong> unite <strong>the</strong>m.” Indeed,<br />

<strong>the</strong> two genera are readily separated morphologically: Lolium has spicate inflorescences<br />

and spikelets with a single glume, while Festuca has paniculate inflorescences and spikelets<br />

with two glumes. The key below is in part modified from Aiken and Lefkovitch (1993). (Latin:<br />

festuca, stalk, stem, or straw; a name used by Pliny for a weed—Darbyshire & Pavlick ined.) (subfamily<br />

Pooideae, tribe Poeae)<br />

REFERENCES: Piper 1906; Terrell 1966, 1967, 1968b; Bulinska-Radomska & Lester 1985b, 1988;<br />

Aiken & Darbyshire 1990; Darbyshire & Warwick 1992; Aiken & Lefkovitch 1993; Darbyshire<br />

1993, ined.; Tucker 1996; Aiken et al. 1997, 1998; Charmet et al. 1997; Soreng & Terrell 1997; Thomas<br />

et al. 1997; Pasakinskiene et al. 1998; Gaut et al. 2000; Soreng et al. 2001; Torrecilla &<br />

Catalán 2002; Darbyshire & Pavlick ined.<br />

1. Inflorescence contracted, at l<strong>east</strong> above, with lower branches <strong>of</strong>ten bearing spikelets well below<br />

<strong>the</strong> middle; spikelets 8–15(–20) mm long, with 3–10 florets; lower lemmas 4–12 mm long; introduced<br />

species usually <strong>of</strong> roadsides, fields, and disturbed or open areas.<br />

2. Auricles at summit <strong>of</strong> leaf sheath usually with ciliate margins; spikelets usually with 3–6 florets;<br />

leaf sheaths with age pale straw-colored, <strong>of</strong>ten staying intact; leaf blades 3–12 mm wide;<br />

lemmas usually 6–12 mm long, usually minutely scabrous (use dissecting scope), with a short<br />

awn 0.3–2(–4) mm long, rarely awnless; rachilla scabrous; shortest branch (if more than one)<br />

at each main node <strong>of</strong> inflorescence usually with 3 or more spikelets; lowest inflorescence<br />

node with 2 or 3 branches ____________________________________________________ F. arundinacea<br />

2. Auricles at summit <strong>of</strong> leaf sheath with glabrous margins; spikelets usually with (4–)6–10 florets;<br />

leaf sheaths with age brown, breaking down <strong>to</strong> form fibers; leaf blades 2–7(–8) mm wide;<br />

lemmas usually 4–6(–8) mm long, usually glabrous or scabrous only at apex, usually awnless;

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