Trichophorum cespitosum |
Trichophorum |
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trichophore cespiteux, tuft bulrush, tuft clubrush, tuft clubsedge |
bulrush, club-rush, deergrass, trichophore |
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Habit | Plants densely cespitose; rhizomes absent. | Herbs, perennial, cespitose, rhizomatous or not. | ||||||||||||||||||||
Culms | grooved, terete, 5–45 cm, smooth. |
trigonous or terete. |
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Leaves | basal sheaths brown; distal leaf sheaths concave at mouth; blades 1.5–8 × 0.3–0.4 mm, much shorter than culms at flowering and fruiting. |
basal or subbasal; sheaths bladeless or distal sheaths with blade to 5 mm, not fibrous; ligules present; blades obsolete or elongate, linear, less than 1 cm × 1 mm. |
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Inflorescences | spikelets 3–9-flowered, 3.3–7 × 1.2–3 mm; bracts equaling spikelets, 3.3–4.5 mm, apex with awn less than 1 mm. |
terminal; spikelets 1; involucral bracts 1, suberect, scalelike, apex mucronate or awned. |
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Spikelets | scales reddish brown to dark brown, apex mucronate to acute. |
scales 3–9, spirally arranged, each subtending flower. |
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Flowers | perianth bristles 6, brown, terete, equaling or exceeding achenes, smooth to scabrous; anthers 1.5–2.6 mm. |
bisexual; perianth of 0–6 bristles, straight, shorter than to about 20 times as long as achene, smooth or scabrous; stamens 3; styles linear, 3-fid, base persistent. |
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Achenes | compressed trigonous, 1.4–1.7 × 0.6–0.9 mm. |
trigonous or plano-convex. |
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2n | = 104. |
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Trichophorum cespitosum |
Trichophorum |
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Phenology | Fruiting summer (May–Aug). | |||||||||||||||||||||
Habitat | Open, wet, rocky or peaty meadows, fens, bogs, shores | |||||||||||||||||||||
Elevation | 0–2100 m (0–6900 ft) | |||||||||||||||||||||
Distribution |
AK; ID; ME; MT; NC; NH; NY; OR; SC; TN; UT; VT; WA; AB; BC; MB; NB; NL; NS; NT; NU; ON; PE; QC; SK; YT; montane c Asia; Greenland; Europe; boreal w Asia
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North America; Circumpolar to circumboreal; Andean and tropical Southeast Asian mountains |
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Discussion | Segregates defined on the basis of characters such as the number of flowers per spike and distal leaf sheath morphology have been recognized at varietal or subspecific ranks in North America and Europe. In North America, at least, these characters are variable within populations and appear to have no geographic integrity. North American plants of Trichophorum cespitosum appear to be identical to subsp. cespitosum (cf. R. A. DeFilipps 1980). No cytological differences have been detected between European and North American populations; all counted plants have 2n = 104 or n = 52. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species 9 (6 in the flora). The appropriate name and typification for this genus have been debated widely. Arguments for conservation of Trichophorum Persoon in the sense used here, with the conserved type, T. alpinum (Linnaeus) Persoon, were presented (M. Salmenkallio and I. Kukkonen 1989), and the proposal was accepted in the Code. The proposal to segregate T. alpinum from the rest of Trichophorum, in the genus Eriophorella (J. Holub 1984), is based on characters that do not justify generic rank. In fact, K. Tan (1985) found that T. pumilum (Vahl) Schinz & Thellung could not be considered generically distinct from T. alpinum and created a combination for it within Eriophorella. The name Baeothryon Ehrhart ex A. Dietrich, previously considered to be a synonym of Trichophorum, has been shown to apply to a section of Eleocharis R. Brown (M. Salmenkallio and I. Kukkonen 1989; M. S. González-Elizondo and P. M. Peterson 1997). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 23, p. 29. | FNA vol. 23, p. 28. | ||||||||||||||||||||
Parent taxa | Cyperaceae > Trichophorum | Cyperaceae | ||||||||||||||||||||
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Synonyms | Scirpus cespitosus, Baeothryon cespitosum, Scirpus bracteatus, Scirpus cespitosus var. callosus, Scirpus cespitosus var. delicatulus | Eriophorella | ||||||||||||||||||||
Name authority | (Linnaeus) Schur: Verh. Mitth. Siebenbürg. Vereins Naturwiss. Hermannstadt 4: 78. (1853) | Persoon: Syn. Pl. 1: 69. (1805) | ||||||||||||||||||||
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