Elymus hystrix |
Poaceae subfam. pooideae |
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bottlebrush grass, eastern bottle-brush grass, glumeless wlldrye |
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Habit | Plants cespitose, not rhizomatous, occasionally glaucous, particularly the spikes. | Plants annual or perennial; sometimes matlike, sometimes cespitose, sometimes stoloniferous, sometimes rhizomatous. | ||||||||||||||||||||||||||||||||||||
Culms | 50-140 cm, usually erect, occasionally geniculate below; nodes 4-8, exposed or concealed, glabrous. |
usually hollow, sometimes solid. |
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Leaves | evenly distributed; sheaths usually glabrous, occasionally pilose, often purplish; auricles usually present, 0.5-3 mm, brown to black; ligules 1-2(3) mm; blades 4-16 mm wide, lax, usually deep glossy green, adaxial surfaces pilose or scabridulous. |
distichous; sheaths usually open to the base, varying to closed for nearly their full length; auricles present or absent; abaxial ligules absent; adaxial ligules scarious or membranous, sometimes puberulent or scabridulous, usually not ciliate, cilia sometimes shorter than the base; pseudopetioles rarely present; blades usually linear, sometimes broadly so, venation parallel; cross sections non-Kranz, mesophyll nonradiate, adaxial palisade layer absent, fusoid and arm cells usually absent; midribs usually simple; adaxial bulliform cells present; stomates with parallel-sided subsidiary cells; epidermes usually lacking bicellular microhairs, sometimes with unicellular microhairs, papillae usually absent, when present, rarely more than 1 per cell. |
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Inflorescences | usually terminal, panicles, spikes, or racemes, usually ebracteate; disarticulation usually below the florets, sometimes below the glumes, at the rachis nodes, or at the inflorescence bases. |
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Spikes | 7-20 cm long, 4-7 cm wide, more or less erect, usually with 2 spikelets per node, rarely with 3 at some nodes; internodes (3)4-8(10) mm long, (0.1)0.2-0.3(0.4) mm thick at the thinnest sections, flexuous, usually glabrous, sometimes scabrous or hirsute, usually with green lateral bands. |
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Spikelets | 10-18 mm, strongly divergent to patent at maturity, with (1)2-4(6) florets, lowest florets functional; disarticulation above the glumes, beneath each floret. |
usually bisexual, infrequently unisexual or mixed, usually laterally compressed or not compressed, occasionally dorsally compressed, with 1-30 sexual florets, distal floret(s) often reduced, infrequently spikelets with 1-2 reduced or staminate basal florets and a single terminal sexual floret. |
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Glumes | usually vestigial, sometimes 1-3 mm long, about 0.1 mm wide, subulate, entire, with no evident veins, occasionally to 10(20) mm long including the undifferentiated awns and differing in length by more than 5 mm, 0.1-0.2 mm wide, setaceous, tapering from the base, usually glabrous, occasionally appressed-puberulent to strigose, sometimes scabrous, usually straight, rarely somewhat curving, margins firm; lemmas 8-11 mm, usually glabrous, occasionally appressed-puberulent to strigose, especially near the margins and apices, awns (12)20-40(47) mm, usually straight, rarely somewhat curving; paleas 7-11 mm, obtuse or truncate, occasionally emarginate; anthers 2.5-5 mm. |
usually 2, upper or lower glumes sometimes absent, rarely both glumes absent; lemmas without uncinate hairs, awned or not, awns single, basal to apical; paleas usually well-developed, sometimes reduced or absent; lodicules 2(3), usually lanceolate and broadly membranous distally, rarely truncate and fleshy, usually not veined or obscurely veined, sometimes distinctly veined, sometimes ciliate; anthers (1, 2)3; ovaries glabrous or sometimes hairy distally, sometimes with an apical appendage; haustorial synergids absent; styles (1)2 (-4), bases close together, sometimes fused. |
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Caryopses | hila linear, elliptic, ovate, or punctate; endosperm usually hard, sometimes soft or liquid, with or without lipids, starch grains compound or simple; embryos less than 1/2 the length of the caryopses; epiblasts usually present; scutellar cleft usually absent; mesocotyl internode usually absent; embryonic leaf margins overlapping, x = 7, 10. |
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Anthesis | mid-June to early July. |
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2n | = 28. |
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Elymus hystrix |
Poaceae subfam. pooideae |
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Distribution |
AL; AR; CT; DC; DE; GA; IA; IL; IN; KS; KY; MA; MD; ME; MI; MN; MO; NC; ND; NE; NH; NJ; NM; NY; OH; OK; PA; RI; SC; SD; TN; VA; VT; WI; WV; MB; NB; NS; ON; QC
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Discussion | Elymus hystrix grows in dry to moist soils in open woods and thickets, especially on base-rich slopes and small stream terraces. It grows throughout most of temperate eastern North America, extending west to Manitoba and Oklahoma, but is absent from the southern portion of the coastal plain. Plants with pubescent lemmas have been recognized as Elymus hystrix var. bigelovianus (Fernald) Bowden. These occur infrequently north of a line from South Dakota through Kentucky to New Jersey, and are often mixed with the typical variety; uniform populations are known in the northeastern United States. Plants with pubescent blades are also more prevalent to the north. Elymus hystrix hybridizes with most eastern species of Elymus. Introgression may account for the considerable variation in glume development and spikelet appression among these species. Lack of glumes may be a recessive character, with even slight glume development indicating introgression (Church 1967b). Plants with relatively well-developed, subequal glumes are presumed to be of hybrid origin. Such plants include most material from the Carolina piedmont region, where E. glabriflorus (p. 296) is the most likely source of introgression. The relatively frequent hybrids with E. virginicus (p. 298) are usually sterile, but Church (1967b) made crosses through three segregating generations. Within the ranges of E. diversiglumis (p. 316), E. svensonii (p. 314), and E. churchii (p. 314;, there appear to be frequent introgressants between these species and E. hystrix. Further east, especially in the Appalachian regions of North Carolina, Virginia, West Virginia, and Maryland (including the shale barrens and nearby), there are scattered plants of E. hystrix with curving awns and, in a few cases, appressed spikelets (Campbell 2002). Whether these represent occasional variation within the E. hystrix gene pool, or whether they are outlying remnants of introgression with E. canadensis (p. 303) during a past eastward extension, is unknown. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
The subfamily Pooideae includes approximately 3300 species, making it the largest subfamily in the Poaceae. It reaches its greatest diversity in cool temperate and boreal regions, extending across the tropics only in high mountains. The circumscription and relationships of tribes within the Pooideae are unsettled (see, for example, Catalan et al. 1997, 2004; Soreng and Davis 1998). In this flora, some previously recognized tribes have been combined with the Poeae. Recognition of some of these as subtribes is well supported; among these is the Hainardieae Greuter (which, at the subtribal level, is called the Parapholiinae Caro). Members of other traditional tribal groupings, such as the Aveneae Dumort., appear to be widely dispersed within the Poeae sensu lato. Further work will probably support the division of the expanded Poeae into additional tribes; there is as yet no clear indication as to what the boundaries of such tribes should be. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 24, p. 316. | FNA vol. 24, p. 57. | ||||||||||||||||||||||||||||||||||||
Parent taxa | Poaceae > subfam. Pooideae > tribe Triticeae > Elymus | Poaceae | ||||||||||||||||||||||||||||||||||||
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Synonyms | Hystrix patula var. bigeloviana, Hystrix patula, E. hystrix var. bigelovianus | |||||||||||||||||||||||||||||||||||||
Name authority | L. | Benth. | ||||||||||||||||||||||||||||||||||||
Web links |