Eleocharis acicularis
Eleocharis elliptica
needle spike-rush, needle spike-rush (spikesedge), needle spikesedge, éléocharide aciculaire
elliptic spike-rush, elliptic spikesedge, slender spike-rush, éléocharide elliptique
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.
subterete to sometimes compressed, to (2–)3 times as wide as thick, often with (4–)5–10 ridges or angles, 5–90 cm × 0.3–0.8 mm, firm to soft, spongy.
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, not splitting, proximally dark red, distally green to stramineous or red, thinly papery to membranous, apex usually red-brown, obtuse to subacute, often callose, tooth to 0.5 mm usually present on some culms.
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.
ovoid, 3–8 × 2–3(–4) mm, apex obtuse (to acute);
proximal scales amplexicaulous, apex entire;
subproximal scale with a flower;
floral scales spreading in fruit, 10–30, 5–7 per mm of rachilla, medium to very dark brown, midrib region often paler, ovate, 1.7–3 × 1–1.5 mm, apex rounded to obtuse (or acute), entire or shallowly notched (emarginate) or sometimes cut to 0.5(–0.7) mm deep, apical colorless hyaline part at least as wide as long, 0.2–0.7 mm, carinate in distal part of spikelet.
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 absent or rarely 1–3, pale brown, to 1/2 of achene length, sparsely retrorsely spinulose;
stamens 3;
anthers orange-brown, 0.8–1.7 mm;
styles 3-fid or some 2-fid.
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.
persistent after scales fall, usually lemon yellow or dark yellow, orange, or medium brown, rarely greenish, obpyriform, nearly equilaterally to compressed-trigonous, often some biconvex, angles evident to prominent, 0.7–1.2 × 0.6–0.9 mm, neck short or absent, finely to coarsely rugulose at 10X, 12–20 horizontal ridges in vertical series, usually finely cancellate at 10–20X.
gray to greenish or brownish, pyramidal to much depressed, (0.05–)0.1–0.2 × 0.15–0.25 mm.
brown to whitish, greatly depressed, apiculate, sometimes pyramidal, 0.1–0.25 × 0.25–0.45 mm.
= 20.
= 38.
Eleocharis acicularis
Eleocharis elliptica
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.)
Eleocharis elliptica is very variable in rhizome thickness, internode length, culm thickness and cross section shape, presence of a tooth on the distal leaf sheath, floral scale shape, stigma number, and achene color, cross section shape, and surface sculpturing. It is difficult to separate E. elliptica from E. tenuis and E. compressa.
Three varieties have been recognized: (1) E. elliptica var. elliptica, characterized by rhizomes 0.5–1.5 mm thick with the longer internodes 2.5–10 mm, culms terete to subterete, and floral scales entire to shallowly emarginate; (2) E. elliptica var. atrata (Svenson) S. G. Smith, characterized by rhizomes 1.5–2.5 mm thick with the longer internodes very crowded to 5 mm, culms often compressed, to 2 times wider than thick, and floral scales mostly emarginate or deeply cut; 3) E. elliptica var. pseudoptera (Svenson) L. J. Harms, herein placed in E. tenuis.
Varieties of Eleocharis elliptica are not formally recognized herein because they intergrade greatly. Eleocharis elliptica var. atrata is intermediate between E. elliptica var. elliptica and E. compressa var. compressa; it has usually been placed in E. compressa but is better placed in E. elliptica because the type of var. atrata is more like E. elliptica (S. G. Smith 2001). Eleocharis tenuis var. pseudoptera Svenson might also be treated as E. elliptica var. pseudoptera following L. J. Harms (1972), who also reported that he produced fertile E. compressa × E. elliptica hybrids. I have not seen voucher specimens for any of the chromosome numbers or hybrids that Harms reported for any of the species and varieties discussed above. My field observations in calcareous fens in Wisconsin suggest that E. elliptica var. elliptica is adapted to microhabitats where the surface soil is permanently saturated by groundwater discharge; E. compressa var. compressa is adapted to microhabitats such as depressions in prairies and exposed limestone that are dry in summer; E. elliptica var. atrata is adapted to microhabitats that are intermediate between those of typical E. elliptica and those of E. compressa (S. G. Smith 2001).
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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