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needle spike-rush, needle spike-rush (spikesedge), needle spikesedge, éléocharide aciculaire

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

Habit Plants perennial; rhizomes 0.25–0.5 mm thick, internodes 5–15 mm, scales fugaceous, rarely evident, translucent, 2 mm. 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

sometimes arching, smooth or 3–12-ridged, terete to sometimes distinctly compressed, 1–60 cm × 0.2–0.5(–0.7) mm, flaccid to rigid.

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 or fugaceous, proximally stramineous to red, distally colorless to stramineous or whitish, closely sheathing to prominently inflated, often splitting adaxially, apex rounded (to acute).

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 or subcylindric, 2–8 × 1–2 mm, apex acute;

floral scales 4–25, 4–6 per mm of rachilla, bright reddish or purplish brown to stramineous, midrib region often green, ovate, 1.5–2.5(–3.5) × 1–1.5 mm, midrib prominent to obscure, apex blunt to acute.

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 mostly absent, uncommonly 2–4, whitish to pale brownish, slender, obscurely retrorsely and spreading-spinulose, shorter than to equaling achene;

stamens 3;

anthers yellow to brown, 0.7–1.5 mm.

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

with angles plus longitudinal ridges ca. 8–12, obscure to prominent, narrowly to broadly obovoid to obpyriform, 2 times to much less than 2 times longer than wide, 0.7–1.1 × 0.35–0.6 mm, trabeculae 30–60, clearly evident to crowded and obscure, spaces between trabeculae sometimes translucent.

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

gray to greenish or brownish, pyramidal to much depressed, (0.05–)0.1–0.2 × 0.15–0.25 mm.

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

2n

= 20.

= 18, 19, 38.

Eleocharis acicularis

Eleocharis macrostachya

Phenology Fruiting spring–fall. Fruiting spring–summer, all year in s Texas and Louisiana.
Habitat Bare, wet soil or in fresh (rarely brackish) lakes, ponds, vernal pools, meadows, springs, disturbed places Fresh to slightly brackish or alkaline shores, stream beds, swales, vernal pools, pastures, ditches, artificial ponds
Elevation 0–3300 m (0–10800 ft) 10–2300 m (0–7500 ft)
Distribution
from FNA
AK; AR; AZ; CA; CO; CT; DC; DE; GA; IA; ID; IL; IN; KS; KY; LA; MA; MD; ME; MI; MN; MO; MS; MT; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OK; OR; PA; RI; SC; SD; TN; TX; UT; VA; VT; WA; WI; WV; WY; AB; BC; MB; NB; NL; NS; NT; NU; ON; PE; QC; SK; YT; Mexico; Central America; Greenland; South America (Ecuador); Eurasia [Australia (probably introduced)]
[WildflowerSearch map]
[BONAP county 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

Eleocharis acicularis is abundant and ecologically important throughout much of its range. It occurs in a wide variety of habitats, including acid waters. I have not seen voucher specimens for reports from Alabama and Florida. I have not seen vouchers for the reported chromosome numbers of 2n = 30–38 or 50–58.

Eleocharis acicularis often forms large rooted mats or floating masses, which when submerged, are often non-flowering. Submerged, usually nonflowering plants are abundant throughout much of the range of the species (H. K. Svenson 1929; P. E. Rothrock and R. H. Wagner 1975). They have been called E. acicularis forma fluitans (Doellinger) Svenson; E. acicularis forma inundata Svenson; E. acicularis forma longicaulis (Desmazières) Hegi; E. acicularis forma submersa (Nilsson) Norman; and E. acicularis var. submersa (Nilsson) Svenson. The culms of the submerged plants are terete, smooth, soft to flaccid, translucent, and the partitions of the air cavities within are clearly visible. Submerged plants may closely resemble aquatic forms of some other species, especially Eleocharis parvula, E. robbinsii, and Schoenoplectus subterminalis (Torrey) Sojak (N. C. Fassett 1957; E. G. Voss 1967, 1972–1996, vol. 3).

Although E. acicularis is very variable, recognition of varieties is premature pending a worldwide taxonomic revision of subg. Scirpidium. Much of the variation is apparently due to phenotypic plasticity in response to environmental factors, especially water depth (P. E. Rothrock and R. H. Wagner 1975). The named varieties intergrade extensively, and achenes, which are important in defining the varieties, are often absent. H. K. Svenson (1929) recognized four varieties and two forms for North America, but later (1957) did not recognize infraspecific taxa.

Most plants from the Arctic to cool-temperate North America, including higher elevations in the Southwest, are very similar to plants from northern Europe and presumably belong to typical E. acicularis, which was described from Europe. Those plants have culms cylindric or three- to four-angled; leaf sheaths mostly obscure and closely sheathing; and achenes about two times longer than wide.

Eleocharis acicularis var. gracilescens Svenson, type from St. Louis, Missouri, applies to plants with flowering culms unusually long (to 60 cm), smooth or sometimes with five to twelve fine ridges, their bases not cormlike; spikelets often linear-lanceoloid, often unusually long (to 8 mm); floral scales often unusually long (to 3.5 mm), often stramineous; and achenes much less than two times longer than wide. Plants of E. acicularis var. gracilescens are probably usually emergent in shallow water; they are known from scattered collections from Alabama, Florida, Kansas, Missouri, North Dakota, Oklahoma, South Carolina, Tennessee, and Texas. Robust plants of E. acicularis var. gracilescens are sometimes misidentified as E. wolfii. H. K. Svenson (1957) stated that var. gracilescens may be distinct from E. acicularis. Some specimens from California and Oregon that resemble E. acicularis var. gracilescens may be ecologic forms of E. acicularis var. occidentalis.

Eleocharis acicularis var. occidentalis Svenson, type from Santa Barbara, California (illustrated in H. L. Mason 1957; H. K. Svenson 1939, plate 539), applies to plants with culms only 2–6 cm, smooth or usually some prominently four-angled or finely to ca. eight-ridged, their bases often persistent, swollen, and cormlike (illustrated herein); distal leaf sheath summits mostly evident, often markedly inflated; achenes much less than two times longer than wide. This variety often grows in vernal pools. As here defined, it is known only from Arizona, California, and Nevada. Most of the specimens H. K. Svenson (1929) cited in the protologue and identified on herbarium specimens as E. acicularis var. occidentalis are probably referable to typical E. acicularis.

Eleocharis acicularis var. porcata S. G. Smith (S. G. Smith 2001), type from Texas, applies to plants that are similar to E. acicularis var. occidentalis except that their culms (cross section illustrated herein) reach 22 cm × 0.5 mm, some or all are prominently six- to twelve-ridged and mostly distinctly compressed, and their bases are not cormlike. This variety grows in mud and shallow water of marshes, ponds, and stream margins; it is known from Alberta, Arizona, Colorado, Illinois, Kansas, Louisiana, Nebraska, New Mexico, North Dakota, and Texas. Because of their compressed, prominently-ridged culms, robust plants of E. acicularis var. porcata, including a paratype of E. wolfii, are sometimes misidentified as E. wolfii (S. G. Smith 2001).

(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. 108. FNA vol. 23, p. 74.
Parent taxa Cyperaceae > Eleocharis > subg. Scirpidium Cyperaceae > Eleocharis > subg. Eleocharis > sect. Eleocharis > ser. Eleocharis
Sibling taxa
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. 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. 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 acicularis, E. acicularis var. gracilescens, E. acicularis var. occidentalis, E. acicularis var. porcata, E. acicularis var. submersa E. perlonga, E. xyridiformis
Name authority (Linnaeus) Roemer & Schultes: in J. J. Roemer et al., Syst. Veg. 2: 154. (1817) Britton: in J. K. Small, Fl. S.E. U.S., 184, 1327. (1903)
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