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

confusing spikerush, creeping spike-rush, pale spike-rush, spike rush, éléocharide à gros épi

Habit 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. Plants perennial, mat-forming; rhizomes evident, long, 1–2 mm thick, firm, cortex persistent, longer internodes 10–55 mm, scales often fugaceous, 5–10 mm, membranous, not fibrous.
Culms

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

terete to markedly compressed, to 3 times wider than thick, often with to 25 blunt ridges when dry, 10–100 cm × 0.5–2.5(–3.5) mm, firm (to soft), internally spongy.

Leaves

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.

distal leaf sheaths persistent, rarely splitting abaxially, proximally mostly red, distally green (or red), papery (to membranous), apex truncate to obtuse, tooth sometimes present on some or all culms, 0.1–0.6(–1) mm.

Spikelets

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.

narrowly lanceoloid to ovoid, 5–40 × 2–5 mm, acute, rarely obtuse;

proximal scale clasping (2/3–)3/4 or more of culm to amplexicaulous, usually variably in same plant;

subproximal scale empty or with flower, usually empty in some spikelets and with flower in other spikelets in same plant;

floral scales deciduous, often spreading in fruit, 30–80, 3–5 per mm of rachilla, medium brown, sometimes red-brown or dark chestnut-brown, midrib regions often stramineous to green, ovate to narrowly lanceolate, 2.5–5.5 × 1.5–2.5 mm, entire, mostly carinate in distal part of spikelet.

Flowers

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.

perianth bristles 4(–5), sometimes rudimentary or absent, brown, slender to stout, much shorter than achene to equaling tubercle;

stamens 3;

anthers dark yellow to orange-brown, 1.3–2.7 mm;

styles 2-fid.

Achenes

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.

not persistent, yellow maturing to yellow-brown or dark brown, ellipsoid, obovoid, or obpyriform, biconvex to plano-convex, angles obscure, 1.1–1.9 × 0.8–1.5 mm, apex rounded, neck absent or short, smooth at 30X, or finely rugulose at 10–20X with 20 or more horizontal ridges in a vertical series.

Tubercles

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.

brown to whitish, pyramidal, as high as or sometimes much higher than wide, 0.35–0.7 × 0.25–0.7 mm.

2n

= 18, 19, 38.

Eleocharis uniglumis

Eleocharis macrostachya

Phenology Fruiting summer. Fruiting spring–summer, all year in s Texas and Louisiana.
Habitat Mostly coastal, brackish (to fresh?) shores, marshes Fresh to slightly brackish or alkaline shores, stream beds, swales, vernal pools, pastures, ditches, artificial ponds
Elevation 0–2300 m (0–7500 ft) 10–2300 m (0–7500 ft)
Distribution
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]
from FNA
AK; AR; AZ; CA; CO; IA; ID; IL; KS; LA; MN; MO; MS; MT; ND; NE; NM; NV; OK; OR; SD; TX; UT; WA; WI; WY; AB; BC; MB; ON; QC; YT; Mexico; South America (Argentina, Colombia, Uruguay)
[WildflowerSearch map]
Discussion

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.)

The chromosome numbers 2n = 10 and 2n = 16 have also been reported from North America but have not been verified.

Eleocharis macrostachya probably occurs in Saskatchewan; I have not seen specimens. It is extremely variable. Cytotaxonomic studies (S.-O. Strandhede 1967; L. J. Harms 1968) and morphology suggest that it is a diploid-polyploid complex at least partly of hybrid origin from E. palustris and both E. erythropoda and E. uniglumis. The 2n = 38 plants of E. macrostachya may comprise the American counterpart of the European E. palustris subsp. vulgaris, which presumably originated from E. palustris subsp. palustris and E. uniglumis (S.-O. Strandhede 1966). Although recognition of infraspecific taxa is premature, the following three intergrading variants are notable:

Variant a (= Eleocharis xyridiformis) almost certainly deserves taxonomic recognition, perhaps as a species. It has markedly compressed culms to 3 times wider than thick; distal leaf-sheath apices subtruncate, usually with a tooth to 0.6(–1) mm on some or all culms; spikelets narrowly lanceoloid; floral scales medium brown to stramineous, mostly lanceolate and carinate, 2.5–4 × 1.5 mm; achenes 1.1–1.5 × 0.8–1.2 mm; chromosome numbers (for which I have seen vouchers, all from Kansas and South Dakota), 2n = 18. It is known from 20–450 m in Arizona, California, Illinois, Kansas, Missouri, New Mexico, Oklahoma, South Dakota, Texas, and Mexico (Coahuila, Durango, Nuevo León). Both the holotype of E. xyridiformis from Mexico and the vouchers of the 2n = 18 chromosome counts reported for E. xyridiformis, all from Kansas and South Dakota, have stomates 55–60 µm, which is typical of 2n = 18 plants (S.-O. Strandhede 1967). The holotype of E. macrostachya from Oklahoma, which is otherwise much like the type of E. xyridiformis except for less markedly compressed culms, has stomates averaging 59–68 µm, which is typical of plants of E. macrostachya with 2n = 38 as in variant b.

Variant b is very variable in comparison with variant a. It differs from variant a in having culms terete or slightly compressed; distal leaf-sheath apices often obtuse, tooth rarely present, to 0.1 mm; spikelets broadly lanceoloid to ovoid; floral scales 3.5–4(–4.5) × 1.7–2+ mm; achenes 1.3–1.5 mm, rarely to 1.8 mm; culm stomates 60–72 µm; chromosome numbers (for which I have seen vouchers, all from Kansas and South Dakota), 2n = ca. 38. It is wide-ranging, known from inland localities at 20–2300 m from Manitoba west to Yukon and British Columbia, south to Alabama, Mississippi, Louisiana, Texas, New Mexico, Arizona, and California, and in Mexico from Baja California. Intermediates between variant b and both Eleocharis erythropoda and E. uniglumis are widespread, and intermediates with E. ambigens occur in Louisiana. Most plants of variant b have floral scales to 4 mm and achenes to 1.5 mm; plants with scales to 4–5 mm and achenes sometimes more than 1.6 mm occur in California, Nevada, Oregon, and Washington.

Variant c differs from variant b in having spikelet scales mostly uniformly dark chestnut-brown, not carinate, (3.5–)4–5.5 × 2–2.5 mm. Its achenes are often unusually large, 1.3–1.8(–2) × 1.1–1.5 mm. It is known from near sea level on the coasts of British Columbia, Ontario, and Quebec (James Bay and Magdalen Islands); Alaska, California, Oregon, and Washington. Some plants are intermediate between variant c and variant b. Several specimens I have seen from far eastern Russia are very similar to American plants of Eleocharis macrostachya, variant c. Except for having incompletely amplexicaulous proximal scales, and subproximal scales often without a flower, variant c closely resembles many Eurasian specimens of E. uniglumis.

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

Source FNA vol. 23, p. 76. FNA vol. 23, p. 74.
Parent taxa Cyperaceae > Eleocharis > subg. Eleocharis > sect. Eleocharis > ser. Eleocharis 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. 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
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. 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. uniglumis, E. vivipara, E. wolfii
Synonyms Scirpus uniglumis, E. halophila, E. uniglumis var. halophila E. perlonga, E. xyridiformis
Name authority (Link) Schultes: Mant. 2: 88. (1824) Britton: in J. K. Small, Fl. S.E. U.S., 184, 1327. (1903)
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