Eleocharis acicularis
Eleocharis obtusetrigona
needle spike-rush, needle spike-rush (spikesedge), needle spikesedge, éléocharide aciculaire
spikerush
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.
obscurely 3–5-angled to terete, 40–110 cm × (2–)3.6–7.5 mm, soft, not septate-nodulose, internally spongy, transverse septa incomplete;
plants never forming filiform, flaccid culms.
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, membranous, apex acute to long-acuminate, sometimes prolonged into a slender bladelike portion to 6 cm.
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.
not proliferous, 12–43 × 3.5–6 mm;
rachilla joints bearing obscure winglike remnants of floral scales;
proximal scale without a flower, amplexicaulous, 3.6–7.5 mm;
floral scales 30–125, 1–3 per mm of rachilla, greenish to pale brown, often with pale to dark brown submarginal band or a subapical darker spot, ovate to oblong, 4.3–5.8 × 2.5–3.3 mm, cartilaginous, often membranous toward margins, margins broadly translucent, membranous, apex rounded to acute.
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 6–7, stramineous, margins and spinules reddish to pale brown, stout, flattened, subequal, exceeding achene, 2.5–3.2 mm, coarsely retrorsely spinulose;
anthers reddish brown, 1.5–1.9 mm;
styles 3-fid or sometimes 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.
pale brown, biconvex, obpyriform, 1.7–2.3 × 1.2–1.5 mm, clearly sculptured at 10–15X, each face with 10–15 rows of transversely elongated cells, often isodiametric at achene base, apex usually constricted to neck 0.5–0.6 mm wide.
gray to greenish or brownish, pyramidal to much depressed, (0.05–)0.1–0.2 × 0.15–0.25 mm.
stramineous, lamelliform to high-pyramidal, 0.8–1.1 × 0.7–0.9 mm.
= 20.
Eleocharis acicularis
Eleocharis obtusetrigona
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.)
In North America Eleocharis obtusetrigona is known from only five collections, two of them originally identified as E. fistulosa (Poiret) Link [= E. acutangula (Roxburgh) Schultes], which is common in Mexico and South America. The original description of E. obtusetrigona is poor and does not clearly distinguish E. obtusangula from E. acutangula. H. K. Svenson (1939) included E. obtusetrigona in E. acutangula, which can be distinguished by its acutely trigonous culms as well as its smaller floral scales and achenes. The tubercles are often spongy as in E. quadrangulata.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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