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

two-tone spikerush

Habit 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. Plants probably perennial, tufted, not stoloniferous; rhizomes present, ± horizontal, 0.2–0.4 mm thick, firm, longer internodes 3–7 mm, scales translucent or not.
Culms

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.

often ascending, often spotted or streaked red-brown, cross section quadrangular or broadly elliptic, often sulcate, 1.5–8(–25) cm × 0.1–0.3 mm, soft.

Leaves

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.

distal leaf sheaths persistent or fugaceous, closely sheathing, not conspicuously wrinkled, colorless or pale brown, sometimes spotted red-brown, delicately membranous, apex narrowly acute.

Spikelets

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.

basal spikelets absent; never proliferous, ovoid or ellipsoid, laterally compressed or terete, 1.5–3.7 × 0.8–3 mm, apex acute;

proximal scale empty, persistent, amplexicaulous, similar to floral scales;

subproximal scale with a flower;

floral scales distichous (spirodistichous), 8–22, 6–10 per mm of rachilla, colorless or pale brown, mottled red-brown to purple, ovate, (1–)2 × 1 mm, membranous, midribs green and red-brown, prominent, apex rounded to obtuse.

Flowers

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.

perianth bristles present or absent, (1–)4, colorless to white, vestigial to shorter than achene, 0–0.55 mm;

spinules not evident at 45X;

stamens (1–)3;

anthers 0.35–0.45 mm;

styles 2-fid (or 3-fid).

Achenes

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.

whitish to pale brown, obovoid, biconvex, rarely trigonous, angles prominent, 0.5–0.8 × 0.4–0.6 mm, apex slightly constricted proximal to tubercle, smooth.

Tubercles

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

sessile, green or red-brown, pyramidal, birettaform or umbonate, 0.15–0.25 × 0.3–0.4 mm.

2n

= 18, 19, 38.

Eleocharis macrostachya

Eleocharis bicolor

Phenology Fruiting spring–summer, all year in s Texas and Louisiana. Fruiting summer–late fall.
Habitat Fresh to slightly brackish or alkaline shores, stream beds, swales, vernal pools, pastures, ditches, artificial ponds Moist banks, freshwater, damp pine barrens
Elevation 10–2300 m (0–7500 ft) 0–50 m (0–200 ft)
Distribution
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]
from FNA
FL; GA; MS; West Indies; Central America (Nicaragua)
Discussion

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.)

Of conservation concern.

The culms of Eleocharis bicolor sometimes have complete transverse septa which are prominent when plants are aquatic.

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

Source FNA vol. 23, p. 74. FNA vol. 23, p. 96.
Parent taxa Cyperaceae > Eleocharis > subg. Eleocharis > sect. Eleocharis > ser. Eleocharis Cyperaceae > Eleocharis > subg. Eleocharis > sect. Eleocharis > ser. Tenuissimae
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. 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
E. acicularis, E. aestuum, E. albida, E. ambigens, E. atropurpurea, E. baldwinii, E. bella, E. bernardina, 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. uniglumis, E. vivipara, E. wolfii
Synonyms E. perlonga, E. xyridiformis
Name authority Britton: in J. K. Small, Fl. S.E. U.S., 184, 1327. (1903) Chapman: Fl. South. U.S., 517. (1860)
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