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CAREX/CYPERACEAE<br />

517<br />

The following key <strong>to</strong> species is based on mature perigynia (= sac-like structure enclosing <strong>the</strong><br />

pistillate flower and later <strong>the</strong> fruit) and fruits (achene); fruiting material is essential for proper<br />

identification. The following specialized terminology may be helpful: infructescence = a mature<br />

inflorescence, in o<strong>the</strong>r words, an inflorescence in fruit; incomplete veins = veins that do not extend<br />

<strong>the</strong> entire length <strong>of</strong> <strong>the</strong> perigynium body; septate-nodulose = with conspicuous cross venation;<br />

androgynous = condition where <strong>the</strong> staminate flowers are distal <strong>to</strong> <strong>the</strong> pistillate flowers;<br />

gynecandrous = condition where <strong>the</strong> pistillate flowers are distal <strong>to</strong> <strong>the</strong> staminate flowers;<br />

abaxial side = side away from <strong>the</strong> axis or dorsal side; adaxial side = side <strong>to</strong>ward <strong>the</strong> axis or ventral<br />

side. Digital images (line drawings) <strong>of</strong> most East TX Carex species are available on-line<br />

(TAMU 1997). (The classical Latin name, <strong>of</strong> obscure origin; possibly from <strong>the</strong> Greek: keirein, <strong>to</strong><br />

cut, on account <strong>of</strong> <strong>the</strong> sharp leaves—as indicated in <strong>the</strong> English name SHEAR-GRASS)<br />

REFERENCES: Kükenthal 1909; Mackenzie 1931—35, 1940; Hermann 1954, 1970; Bryson 1980;<br />

Reznicek & Ball 1980; Menapace et al. 1986; Tucker 1987; Standley 1989, 1990, 2002a, 2002b,<br />

2002c; Ball 1990; Bernard 1990; Crins 1990; Jones & Hatch 1990; Manhart 1990; Naczi 1990, 1992,<br />

2000, 2002; Naczi & Bryson 1990; Reznicek 1990, 2002a, 2002b, 2002c; Jones & Reznicek 1991,<br />

1995; Jones et al. 1991a, 1991b; Rothrock 1991; Cayouette & Catling 1992; Jones & Jones 1993;<br />

Reznicek & Naczi 1993; Jones 1994a, 1994b; Rothrock & Reznicek 1996a, 1996b, 2001, 2002;<br />

Ford et al. 1998; Hyatt 1998; Naczi et al. 1998, 2002; Miller et al. 1999; Mohlenbrock 1999; Starr et<br />

al. 1999; Yen & Olmstead 2000a, 2000b; Roalson et al. 2001; Rosen 2001; Ball 2002a, 2002b,<br />

2002c; Ball & Reznicek 2002; Bryson & Naczi 2002a, 2002b; Cochrane 2002a, 2002b;<br />

Cochrane & Naczi 2002; Crins & Rettig 2002; Crins et al. 2002; Ford & Reznicek 2002;<br />

Mastrogiuseppe et al. 2002; Naczi & Bryson 2002; Reznicek & Catling 2002; Reznicek & Ford<br />

2002; Standley et al. 2002; Waterway 2002; Downer & Hyatt 2003; MacRoberts et al. 2004;<br />

Starr et al. 2004.<br />

1. Achenes 2–sided, plano-convex or unequally biconvex in transverse-section; stigmas 2.<br />

2. Infructescence (= inflorescence in fruit) 2–5 cm wide, usually an open or contracted panicle<br />

<strong>of</strong> spicate branches.<br />

3. Perigynia with beak as long as or longer than <strong>the</strong> body; dorsal surface <strong>of</strong> leaf sheaths green<br />

without white dots; ventral leaf sheath margins with orange-red dots; achenes ovate-<br />

3. Perigynia with beak shorter than <strong>the</strong> body; dorsal surface <strong>of</strong> leaf sheath dark blue-green<br />

with conspicuous white dots; ventral leaf sheath margins without orange-red dots; achenes<br />

broadly ovate; perigynial wall little <strong>to</strong> not at all adhering <strong>to</strong> achene ________________ C. oklahomensis<br />

2. Infructescence less than 1.5 cm wide, a contracted panicle <strong>of</strong> spicate branches, spicate racemes,<br />

or composed <strong>of</strong> terminal, lateral, or terminal and lateral spikes.<br />

4. Terminal spike solely staminate, or sometimes partly pistillate as in some specimens <strong>of</strong> C.<br />

crinita.<br />

5. Lateral spikes conspicuously peduncled, drooping or not _______________ C. crinita var. brevicrinis<br />

5. Lateral spikes, at l<strong>east</strong> <strong>the</strong> lower, sessile or nearly so, ascending.<br />

6. At maturity leaf sheaths becoming fimbriate filiferous, hyaline material between veins<br />

fugacious, leaving only a reticulate network <strong>of</strong> veins; lower lateral spikes usually remote;<br />

perigynia granular-papillate in upper half __________________________________ C. stricta<br />

6. At maturity leaf sheath not becoming fimbriate filiferous, hyaline material between<br />

veins not fugacious, not leaving a reticulate network <strong>of</strong> veins, instead leaving leaf<br />

sheath intact; lower lateral spikes overlapping; perigynia granular-papillate only<br />

apically _________________________________________________________________ C. emoryi<br />

4. Terminal spike ei<strong>the</strong>r androgynous or gynecandrous.<br />

7. Terminal or all spikes androgynous (in some species <strong>the</strong> staminate flowers <strong>of</strong>ten fugacious,<br />

making spikes appear solely pistillate); spikes not appearing clavate.<br />

8. Primary spicate branches usually less than 10, most frequently <strong>the</strong> primary branches<br />

comprised <strong>of</strong> a single spike, infrequently rebranching giving rise <strong>to</strong> secondary spikes.

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