Flora of North America species comparison

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Eleocharis uniglumis

Eleocharis fallax

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

creeping spikerush, creeping spikesedge
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 5–10(–20) mm, scales sometimes fugaceous, 5–7 mm, papery (to membranous), sometimes fibrous.
Culms

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

terete, often with to 12 blunt ridges when dry, 30–75 cm × 0.5–1.5 mm, firm, 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, not splitting, proximally dark red, distally stramineous or green, papery to membranous, apex dark redbrown, obtuse, not callose, tooth rarely present on some culms, 0.2 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.

ovoid or subspheric, 5–12 × 2–3(–4) mm, apex acute to obtuse;

proximal scale amplexicaulous, entire;

subproximal scale with flower;

floral scales deciduous, often spreading in fruit, 10–35, 3 per mm of rachilla, red-brown to blackish brown, midrib regions sometimes green, ovate, 2.5–3 × 1.7 mm, apex entire, obtuse to acute, often 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 1–5, brown, stout, very unequal, rudimentary to equaling achene;

stamens unknown [absent from specimens];

styles 3-fid or some 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, dark yellow or medium brown, obovoid to obpyriform, compressed trigonous, or some thickly biconvex, angles evident, 1.1–1.5 × 0.95–1.25 mm, apex rounded, neck very short (to absent), finely rugulose at 10–20X, 20 or more horizontal ridges in vertical series, finely cancellate at 20–30X.
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.

whitish to brown, pyramidal, not depressed, as high as wide, 0.3–0.5 × 0.4–0.6 mm.
2n

= 42.

Eleocharis uniglumis

Eleocharis fallax
Phenology Fruiting summer. Fruiting late summer.
Habitat Mostly coastal, brackish (to fresh?) shores, marshes Coastal, fresh to brackish pond and lakeshores, marsh
Elevation 0–2300 m (0–7500 ft) 0–10 m (0–0 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
MA; NJ; NS
[BONAP county 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.)

Of conservation concern.

The taxonomic status of Eleocharis fallax is problematic. I have seen only the type, from 1919 from a pond on Cape Cod, Massachusetts; a specimen from 1955 from Inverness County, Nova Scotia; and a specimen from the Passaic River marshes in New Jersey. It is reportedly extirpated from the type locality (M. L. Fernald 1950). Another specimen from Cape Cod is typical of E. fallax except for some lenticular achenes. I have not seen a voucher for the material, reportedly collected by H. K. Svenson from a brackish marsh on Plum Island, Essex County, Massachusetts, from which S.-O. Strandhede (1967) counted the chromosome number. It seems possible that these collections are of hybrid origin from E. elliptica and either E. erythropoda or E. uniglumis var. halophila (M. L. Fernald 1950). The plants are similar to E. erythropoda except for their trigonous, rougher achenes and sometimes fibrous rhizome scales, which suggests introgression from E. elliptica. Because some specimens of E. ambigens, including the type, have mixtures of lenticular and trigonous achenes, E. fallax is often treated as conspecific with E. ambigens, from which it differs only in its 3-fid styles, trigonous, more rugulose achenes, and higher tubercles. It seems best to recognize E. fallax as a species pending further research because the plants bear many, apparently normal achenes and are not exactly intermediate between their putative parents, and to avoid using a name for the widespread E. ambigens that may apply only to rare hybrids.

(Discussion copyrighted by Flora of North America; reprinted with permission.)
Source FNA vol. 23, p. 76. FNA vol. 23, p. 78.
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. 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 Scirpus uniglumis, E. halophila, E. uniglumis var. halophila
Name authority (Link) Schultes: Mant. 2: 88. (1824) Weatherby: Rhodora 24: 23. (1922)
Web links 
Unless otherwise noted, all data comes from the online version of the Flora of North America, who have made most of their content available via a Creative Commons license (CC BY 4.0).



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