Eleocharis ovata |
Eleocharis occulta |
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ovate spike-rush, ovoid spike-rush, ovoid spikesedge, éléocharide ovale |
limestone spike-rush |
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Habit | Plants perennial, densely cespitose; rhizomes concealed by persistent dead culm bases, often ascending, short, 3–5 mm thick, hard, cortex persistent, internodes very short, scales decaying to coarse fibers, 5–12 mm, papery. | |
Culms | 2–35 cm × 0.3–1 mm. |
subterete to slightly compressed, less than 2 times wider than thick, with 4–7 blunt ridges when dry, 27–56 cm × 0.2–0.5(–0.7) mm, firm to hard, spongy. |
Leaves | apex of distal leaf sheath obtuse to acute, tooth to 0.2 mm. |
distal leaf sheaths persistent, not splitting, proximally red, distally green to stramineous, often inflated, thinly papery to membranous, sometimes translucent, apex broadly obtuse to subtruncate, often callose, tooth absent. |
Spikelets | ovoid, 2–8 × 2–4 mm, apex acute (to blunt); floral scales 25–100+, ca. 10 per mm of rachilla, orange-brown, rarely stramineous, ovate, 1.5–2 × 1 mm, midribs often keeled in distal part of spikelet, apex rounded to subacute. |
ovoid, 3–10 × 2–3 mm, apex acute; proximal scale amplexicaulous, apex 2-fid; subproximal scale with a flower; floral scales spreading in fruit, 20–50, 7 per mm of rachilla, medium brown, midrib region often narrowly stramineous, carinate, lanceolate-attenuate, 2–2.8 × 1 mm, apex 2-fid. |
Flowers | perianth bristles present, rarely absent, (5–)6–7, brown, fairly slender, exceeding tubercle; stamens 2(–3); anthers brown, 0.3 mm; styles 2-fid or some 3-fid. |
perianth bristles 3 or absent, stramineous to pale brown, rudimentary to 1/2 achene length, obscurely retrorsely spinulose; stamens 3; anthers orange-brown, 0.7–1.3 mm; styles 3-fid. |
Achenes | 0.75–1 × 0.6–0.85 mm. |
falling with scales, medium or dark brown, obpyriform, nearly equilaterally obscurely trigonous or cross section nearly circular, 0.7–1 × 0.5–0.65 mm, neck distinct or rarely absent, obscurely rugulose at 10–30X, 30 or more low, blunt horizontal ridges in vertical series. |
Tubercles | deltoid, 0.3–0.5 × 0.3–0.5 mm, 3/5 of to as high as wide, 1/3–2/3 as high and 1/2–3/4 as wide as achene. |
brown, depressed-pyramidal, often rudimentary, 0.1–0.15 × 0.2 mm. |
2n | = 10. |
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Eleocharis ovata |
Eleocharis occulta |
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Phenology | Fruiting summer–fall. | Fruiting spring (Mar–May), sometimes summer (Jul). |
Habitat | Fresh, often drying shores, lake and stream beds, bogs, tidal estuaries, disturbed places | Seasonally wet, calcareous seeps, depressions, swales, rock crevises, rocky stream beds, stream banks, wet meadows, pond margins, often on limestone |
Elevation | 10–700 m (East), 1500–2000 m (Arizona) (0–2300 ft (East), 4900–6600 ft (Arizona)) | 80–300 m (300–1000 ft) |
Distribution |
AZ; CT; IA; IL; IN; KY; MA; ME; MI; MN; MO; NH; NJ; NY; OH; OK; OR; PA; VA; VT; WA; WI; WV; AB; BC; NB; NL; NS; ON; PE; QC; Eurasia
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OK; TX |
Discussion | Although Eleocharis ovata has often been confused with E. obtusa, B. M. H. Larson and P. M. Catling (1996) showed that these species may be distinguished by non-overlapping widths of the tubercles, at least in Canada. The records of E. ovata in New Brunswick, Newfoundland, Nova Scotia, and Prince Edward Island are based on B. M. H. Larson and P. M. Catling (1996) and the records in Illinois, Indiana, Missouri, Montana, New Jersey, Oregon, and Washington are based on D. M. Hines (1975). Eleocharis ovata probably also occurs in Manitoba and Saskatchewan. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Eleocharis occulta is very invariable in contrast to the extreme variability of E. compressa. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 23, p. 103. | FNA vol. 23, p. 83. |
Parent taxa | Cyperaceae > Eleocharis > subg. Eleocharis > sect. Eleogenus > ser. Ovatae | Cyperaceae > Eleocharis > subg. Eleocharis > sect. Eleocharis > ser. Eleocharis |
Sibling taxa | ||
Synonyms | Scirpus ovatus, E. obtusa var. ovata, E. ovata var. heuseri | |
Name authority | (Roth) Roemer & Schultes: in J. J. Roemer et al., Syst. Veg. 2: 152. (1817) | S. G. Smith: Novon 11: 247, figs. 2, 3E–K. (2001) |
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