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few-flower spike-rush, few-flower spikesedge, éléocharide à cinq fleurs

creeping spike-rush, one-glumed spikesedge, onescale spikerush, slender spike-rush, éléocharide unigume

Habit Plants perennial; rhizomes 0.2–1 mm thick, scales persistent or fugaceous, 2–4(–7) mm, thinly membranous, not fibrous; resting buds often present on rhizomes or among culm bases, broadly to narrowly ovoid, 3–6(–10) × 2–5 mm; caudices absent, rarely present, soft or rarely hard, 0.5 mm thick. Plants perennial, mat-forming; rhizomes evident, long, 0.3–1 mm thick, soft to firm, cortex often fugaceous, longer internodes 10–25 mm, scales fugaceous, 5–6 mm, membranous, not fibrous.
Culms

erect, not spirally twisted, not contracted near spikelet, when dry usually with several blunt to acute ridges and sulcate, subterete to slightly compressed, to 2 times wider than thick, 5–35 cm × 0.2–0.5(–1.2) mm, soft to hard;

culm tufts often proximally bulbous (if bulbous then tunicated by papery-fibrous scales).

terete, often with some blunt ridges when dry, (5–)10–60 cm × 0.2–1.5 mm, firm, internally spongy.

Leaves

distal leaf sheaths stramineous to brown or reddish proximally, green to stramineous or brown distally, membranous to papery, apex often reddish, subtruncate to acute.

distal leaf sheaths persistent, not splitting, proximally red, distally stramineous to green, often callose, thinly papery to thickly membranous, apex often dark red-brown, obtuse to subacute, tooth absent.

Spikelets

3–8 × 1.5–4 mm;

proximal scale with a flower, seldom empty, 2–5 mm, 1/2 or more as long as spikelet;

floral scales 3–10 per spikelet, 2.5–6 × 1.5–2.5 mm.

ovoid to lanceoloid, 5–10 × 2–3(–4) mm, apex acute;

proximal scale amplexicaulous, entire;

subproximal scale with flower;

floral scales often spreading in fruit, 10–20, 3–4 per mm of rachilla, brown to often red-brown, midrib regions mostly stramineous to green, broadly ovate, 3–4 × 1.8–2.5 mm, entire, apex acute to obtuse, often some carinate in distal part of spikelet.

Flowers

perianth bristles (0–)3–6, often unequal, rudimentary to equaling tubercle, stout to slender, spinules dense to apparently absent;

anthers 1.5–2.7(–3.5) mm.

perianth bristles 0–4(–5), light brown to stramineous, stout, usually unequal, rudimentary to equaling achene;

stamens 3;

anthers dark yellow to stramineous, 1.2–2 mm;

styles 2-fid.

Achenes

stramineous to medium brown or gray-brown, equilaterally trigonous to compressed-trigonous, rarely some biconvex, obpyriform (to obovoid), 1.6–2.3 × 0.7–1.3 mm, beak variable.

not persistent, dark yellow or medium or dark brown, ellipsoid, obovoid, or obpyriform, biconvex, angles obscure, 1.3–1.8 × 1–1.4 mm, apex rounded, neck absent or short, smooth at 30X, or sometimes finely rugulose at 10–20X with 20 or more horizontal ridges in vertical series.

Tubercles

rarely absent, 0.3–0.4 × 0.2–0.3 mm.

brown to whitish, pyramidal, much higher than wide to slightly depressed, sometimes spongy and with vertical rows of depressions, 0.4–0.8 × 0.3–0.8 mm.

Eleocharis quinqueflora

Eleocharis uniglumis

Phenology Fruiting (spring–)summer. Fruiting summer.
Habitat Fens, wet meadows, seeps, springs, hot springs Mostly coastal, brackish (to fresh?) shores, marshes
Elevation 0–3600 m (0–11800 ft) 0–2300 m (0–7500 ft)
Distribution
from FNA
AK; AZ; CA; CO; IA; ID; IL; IN; MA; ME; MI; MN; MT; NE; NH; NJ; NM; NV; NY; OH; OR; PA; UT; VT; WA; WI; WY; AB; BC; MB; NB; NL; NS; NT; ON; PE; QC; SK; YT; Greenland; Eurasia
[WildflowerSearch map]
[BONAP county map]
from FNA
CO; DE; MA; ME; NC; ND; NE; NH; NJ; NM; NV; NY; RI; SD; UT; VA; AB; BC; MB; NB; NL; NS; NT; ON; PE; QC; Eurasia
[WildflowerSearch map]
Discussion

The chromosome numbers for Eleocharis quinqueflora reported for North America (2n = 80) are in doubt because vouchers and other information are lacking. The often-cited n = 10 is probably erroneous. S.-O. Strandhede and R. M. T. Dahlgren (1968) gave 2n = 132 and 134 from Scandinavia. Recognition of infraspecific taxa within E. quinqueflora is premature pending a worldwide revision of subg. Zinserlingia. It has been reported from North Dakota, although I have not seen specimens. About five varieties and subspecies of E. quinqueflora have been described worldwide.

Most specimens from eastern North America and some from the West can be placed in Eleocharis quinqueflora subsp. fernaldii (Svenson) Hultén, which is characterized by its small size (culms to 15 cm × 0.5 mm) and small bulbs. Specimens of E. quinqueflora from 2000–3600 m in California, which are atypical, especially in that the proximal scales of the spikelets do not subtend flowers, may deserve taxonomic recognition. Those plants are also small, with culms only to 15 cm × 0.5 mm; hard caudices are often present at the culm-tuft bases; small, narrowly ovoid bulbs are sometimes present; and perianth bristles are absent or rudimentary. Very few specimens of E. quinqueflora are intermediate with E. suksdorfiana.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Plants treated as Eleocharis uniglumis fall within the large morphologic variation of Eurasian E. uniglumis. Two subspecies and 3 varieties were recognized for northern Europe (S.-O. Strandhede 1966), and five species that were recognized by I. D. Zinserling (1935) were placed in synonymy under E. uniglumis (S.-O. Strandhede 1966). Recognition of infraspecific taxa within North American E. uniglumis is premature. Plants commonly called E. halophila or E. uniglumis var. halophila, found mostly in Atlantic Coastal brackish habitats, have floral scales that are usually narrower and more densely placed on the rachilla than plants usually called E. uniglumis, which are found mostly in the interior; some plants are intermediate in expression of these characters. The achene and tubercle shape characters used by M. L. Fernald (1950) to distinguish E. uniglumis from E. halophila are not valid. In North America, E. uniglumis is difficult to separate from E. erythropoda and E. kamtschatica, in both of which the spikelets have only the proximal scale without a flower (empty) and the proximal scale completely amplexicaulous. Eleocharis uniglumis differs from E. erythropoda only in its broader floral scales, which are less densely placed on the rachilla; it differs from E. kamtschatica only in its smaller tubercles. It is also difficult to separate from some specimens of E. macrostachya in which the spikelets have proximal scales that are sometimes completely amplexicaulous; such plants differ from E. uniglumis only in the absence of a flower in the axil of the subproximal scale of some of the spikelets. I have not seen voucher specimens for the chromosome numbers of 2n = 27 and 28 reported by S.-O. Strandhede (1967) from Massachusetts and Nebraska, which are lower than the 2n = (44–)46(47–88) reported for Europe (S.-O. Strandhede 1965).

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Source FNA vol. 23, p. 114. FNA vol. 23, p. 76.
Parent taxa Cyperaceae > Eleocharis > subg. Zinserlingia Cyperaceae > Eleocharis > subg. Eleocharis > sect. Eleocharis > ser. Eleocharis
Sibling taxa
E. acicularis, E. aestuum, E. albida, E. ambigens, E. atropurpurea, E. baldwinii, E. bella, E. bernardina, E. bicolor, E. bifida, E. bolanderi, E. brachycarpa, E. brittonii, E. cancellata, E. cellulosa, E. coloradoensis, E. compressa, E. cylindrica, E. decumbens, E. diandra, E. elliptica, E. elongata, E. engelmannii, E. equisetoides, E. erythropoda, E. fallax, E. flavescens, E. geniculata, E. intermedia, E. interstincta, E. kamtschatica, E. lanceolata, E. macrostachya, E. mamillata, E. melanocarpa, E. microcarpa, E. minima, E. montana, E. montevidensis, E. nana, E. nigrescens, E. nitida, E. obtusa, E. obtusetrigona, E. occulta, E. ovata, E. pachycarpa, E. palustris, E. parishii, E. parvula, E. quadrangulata, E. radicans, E. ravenelii, E. retroflexa, E. reverchonii, E. robbinsii, E. rostellata, E. suksdorfiana, E. tenuis, E. torticulmis, E. tortilis, E. tricostata, E. tuberculosa, E. uniglumis, E. vivipara, E. wolfii
E. acicularis, E. aestuum, E. albida, E. ambigens, E. atropurpurea, E. baldwinii, E. bella, E. bernardina, E. bicolor, E. bifida, E. bolanderi, E. brachycarpa, E. brittonii, E. cancellata, E. cellulosa, E. coloradoensis, E. compressa, E. cylindrica, E. decumbens, E. diandra, E. elliptica, E. elongata, E. engelmannii, E. equisetoides, E. erythropoda, E. fallax, E. flavescens, E. geniculata, E. intermedia, E. interstincta, E. kamtschatica, E. lanceolata, E. macrostachya, E. mamillata, E. melanocarpa, E. microcarpa, E. minima, E. montana, E. montevidensis, E. nana, E. nigrescens, E. nitida, E. obtusa, E. obtusetrigona, E. occulta, E. ovata, E. pachycarpa, E. palustris, E. parishii, E. parvula, E. quadrangulata, E. quinqueflora, E. radicans, E. ravenelii, E. retroflexa, E. reverchonii, E. robbinsii, E. rostellata, E. suksdorfiana, E. tenuis, E. torticulmis, E. tortilis, E. tricostata, E. tuberculosa, E. vivipara, E. wolfii
Synonyms Scirpus quinqueflorus, E. fernaldii, E. pauciflora, E. pauciflora var. fernaldii, E. quinqueflora subsp. fernaldii Scirpus uniglumis, E. halophila, E. uniglumis var. halophila
Name authority (Hartmann) O. Schwarz: Mitt. Thüring. Bot. Ges. 1: 89. (1949) (Link) Schultes: Mant. 2: 88. (1824)
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