The green links below add additional plants to the comparison table. Blue links lead to other Web sites.
enable glossary links

pine reed grass, pinegrass

reed grass

Habit Plants sometimes with sterile culms; sometimes loosely cespitose, usually with rhizomes 15+ cm long, 1.5-2 mm thick. Plants perennial; often cespitose, usually rhizomatous.
Culms

(50)60-100(105) cm, unbranched, usually smooth, rarely slightly scabrous beneath the panicles;

nodes (1)2-3(4).

10-210 cm, unbranched or branched, more or less smooth, nodes 1-8.

Sheaths

smooth or slightly scabrous;

collars often hairy, rarely glabrous;

ligules (2)3-5(6) mm, truncate to obtuse, often lacerate;

blades (6)8-40(42) cm long, (1)2-5(8) mm wide, usually flat, abaxial surfaces smooth or slightly scabrous, adaxial surfaces smooth or scabrous, glabrous or sparsely hairy.

open, smooth or scabrous;

auricles absent;

ligules membranous, usually truncate to obtuse, sometimes acute, entire or lacerate, lacerations often obscuring the shapes;

blades flat to involute, smooth or scabrous, rarely with hairs.

Panicles

(5)6-15(25) cm long, (0.7)1.5-2(2.7) cm wide, contracted to somewhat open, erect, usually greenish, infrequently purplish;

branches (1.2)2-4(10) cm, usually slightly scabrous, rarely densely long-scabrous, spikelet-bearing to the base.

Inflorescences

panicles, open or contracted, sometimes spikelike;

branches appressed to more or less drooping, some branches longer than 1 cm.

Spikelets

(3)4-4.5(5.5) mm;

rachilla prolongations 0.6-1.5(2) mm, hairs 1.2-2 mm.

pedicellate, weakly laterally compressed, with 1(2) florets;

rachillas prolonged beyond the base of the distal floret(s), usually hairy;

disarticulation above the glumes.

Glumes

rounded to slightly keeled, mostly smooth, keels rarely slightly scabrous, lateral veins usually obscure, rarely prominent, apices acute;

callus hairs (0.5)1-1.5(2.5) mm, 0.2-0.5(0.7) times as long as the lemmas, sparse;

lemmas 2.5-3.5(4) mm, (0.5)1-2 mm shorter than the glumes;

awns 2.8-3.5(4.5) mm, usually attached to the lower 1/5 of the lemmas, rarely higher, exserted, stout and readily distinguished from the callus hairs, strongly bent;

anthers (1)1.3-2(2.6) mm.

membranous, subequal, equal to, or longer than the lemmas, rounded or keeled, backs smooth or scabrous, rarely long-scabrous with bent projections, veins obscure to prominent, apices acute to acuminate, rarely awn-tipped or attenuate;

lower glumes 1(3)-veined;

upper glumes 3-veined;

calluses hairy, hairs 0.2-6.5 mm, sparse to abundant;

lemmas 3(5)-veined, smooth or scabrous, apices usually tapering into 4 teeth, awned;

awns arising from near the base to near the apices, straight or bent, sometimes delicate and indistinct from the callus hairs, sometimes exserted beyond the lemma margins;

paleas well developed, almost as long as to slightly longer than the lemmas, thin, 2-veined;

anthers 3, sometimes sterile.

Caryopses

shorter than the lemmas, concealed at maturity, oblong, usually glabrous, x = 7.

2n

= 28, 42, 56.

Calamagrostis rubescens

Calamagrostis

Distribution
from FNA
CA; CO; ID; MT; NV; OR; UT; WA; WY; AB; BC; MB; SK
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; AL; AR; AZ; CA; CO; CT; DC; DE; GA; IA; ID; IL; IN; KS; KY; LA; MA; MD; ME; MI; MN; MO; MT; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OR; PA; RI; SC; SD; TN; UT; VA; VT; WA; WI; WV; WY; HI; AB; BC; MB; NB; NL; NS; NT; NU; ON; PE; QC; SK; YT; Greenland
[BONAP county map]
Discussion

Calamagrostis rubescens grows at 50-2800 m, usually in open montane pine or aspen forests and parklands, infrequently in sagebrush steppes, chaparral, and meadows. It is primarily a species of interior western North America, although it reaches the Pacific coast in southern California. The distribution extends from central British Columbia and Alberta east to the Cypress Hills of eastern Alberta and the Pasquia and Cub hills of Saskatchewan, south to western California, Nevada, northeastern Utah, and central Colorado. It is considered threatened in Saskatchewan.

Calamagrostis rubescens is similar to C. koelerioides (p. 721). The two have traditionally been distinguished by the presence of hairs on the leaf collars of C. rubescens, and their absence from C. koelerioides; a more reliable differentiation is the shorter lemmas, glumes, and awns of C. rubescens. Calamagrostis rubescens and C. porteri (p. 721) appear to be closely related. They may be part of the general phenomenon of eastern and western vicariants.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Calamagrostis grows in cool-temperate regions and is especially diverse in mountainous regions. Its species grow in both moist and xeric habitats. There are about 100 species of Calamagrostis, if Deyeuxia Clarion ex P. Beauv. and Lachnagrostis are recognized as distinct from Calamagrostis. The latter two genera are often considered to be restricted to the Southern Hemisphere (Edgar 1995; Jacobs 2001). According to the criteria used by Phillips and Chen (2003) to distinguish Calamagrostis and Deyeuxia, most North American species of Calamagrostis fit within Deyeuxia. There has been insufficient time to evaluate the merits of their recommendation, adoption of which would require many new combinations.

Twenty-five species of Calamagrostis grow in the Flora region; one, C. epigejos, is introduced. Some species of Calamagrostis are rangeland forage grasses, but most occur too sparsely to be important for livestock. Agriculture Canada in Alberta experimented with cultivation of some western species during the 1960s and 1970s.

This treatment includes one cultivar, Calamagrostis ×acutiflora 'Karl Foerster', that is becoming increasingly popular in horticulture. A cultivar of C. canadensis has been registered for use in revegetation in arctic Alaska.

Interspecific hybridization is common; vivipary and agamospermy also occur in some species. Interspecific hybridization, polyploidy, and apomixis contribute to the taxonomic difficulty of the genus.

Some species of Calamagrostis are of interest because of their restricted distributions. These include: C. howellii (Columbia Gorge in Washington and Oregon); C. tweedyi (Washington, Oregon, and Montana); C. tacomensis (Washington and Oregon); C. ophitidis, C. foliosa, C. muiriana, and C. bolanderi (California); C. breweri (California and Oregon); and C. cainii (North Carolina and Tennessee). An incomplete draft treatment of this genus was prepared by Craig W. Greene in 1993, with minor revisions made until 1999. After Greene's death in 2003, completion of the treatment was taken up by Marr and Hebda. The taxa recognized here essentially follow Greene's concepts, with the following exceptions: Calamagrostis breweri sensu Greene (1993) has been split into C. muiriana and C. breweri sensu Wilson and Gray (2002); C. tacomensis is recognized as a species distinct from C. sesquiflora; and C. purpurascens var. laricina Louis-Marie and C. striata subsp. borealis (C. Laest.) Á. Löve & D. Love are not recognized. Descriptions of eastern North American taxa are largely based on Greene's (1980) observations. Northwestern North American taxa are described on the basis of Marr and Hebda's data and field experience. Other western United States taxa were also examined as herbarium specimens; their descriptions include observations by Marr and Hebda. Greene's key was rewritten to conform with the new data.

There is a high degree of misidentification of taxa within this genus (30% for some species in some herbaria), and species distributions should be taken as a guide only. Much more field collecting is needed for several of the taxa in order to verify their distributions, especially near the limits of their ranges. Calamagrostis is sometimes confused with Agrostis; there is no single character that distinguishes all species of Calamagrostis from those of Agrostis. In general, Calamagrostis has larger plants with larger, more substantial lemmas and paleas than Agrostis, and tends to occupy wetter habitats.

Measurements of the rachilla and callus hairs reflect the longest hairs present. Panicle widths refer to pressed specimens.The following key will enable typical specimens to be identified readily, but atypical specimens are common. For this reason, most leads require observation of a combination of characters, notably awn length, length of callus hairs relative to the lemma, glume length and scabrosity, panicle size, and leaf width.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Callus hairs more than 1.3 times as long as the lemmas; lemmas at least 2 mm shorter than the glumes, long-acuminate
C. epigejos
1. Callus hairs usually less than 1.2 times as long as the lemmas; if the callus hairs longer than the lemmas, then the lemmas less than 2 mm shorter than the glumes and not long-acuminate.
→ 2
2. Blades usually densely hairy on the adaxial surfaces; glumes keeled, scabrous; awns 4.5-9 mm long
C. purpurascens
2. Blades glabrous or sparsely hairy on the adaxial surfaces; glumes keeled or rounded, scabrous or smooth; awns 0.5-17 mm long.
→ 3
3. Leaves with abundant white glands between the veins, visible at about 10x; awns 5-8 mm long; plants of California
C. ophitidis
3. Leaves without abundant white glands between the veins; awns 0.5-17 mm long; plants from throughout the Flora region, including California.
→ 4
4. Awns 5-17 mm long, always exserted and bent; if the awns 5-6 mm long, either some blades wider than 2 mm or the abaxial blade surfaces scabrous.
→ 5
5. Panicles open, (2)3.5-6.5(8) cm wide when pressed, branches spikelet-bearing only beyond midlength; awns 10-16 mm long
C. howellii
5. Panicles usually contracted, (0.5)0.8-3 cm wide if open, the branches spikelet-bearing to below midlength, usually to the base; awns 5-17 mm long.
→ 6
6. Some leaf blades 6-13 mm wide; culms (47)60-120(150) cm tall
C. tweedyi
6. All leaf blades (1.5)2-7 mm wide; culms (15)30-60(95) cm tall, if the culms taller than 60 cm, then the blades less than 4 mm wide.
→ 7
7. Awns 12-14(17) mm long; plants of California
C. foliosa
7. Awns (5.4)7-11(13) mm long; plants of Alaska, British Columbia, Washington, and Oregon.
→ 8
8. Glume apices long-acuminate, usually twisted distally; glume keels usually scabrous for their whole length
C. sesquiflora
8. Glume apices usually acute, if acuminate, not twisted distally; glume keels smooth or sparsely scabrous on the distal 1/2
C. tacomensis
4. Awns 0.5-6 mm long, exserted or not, bent or straight; if the awns 5-6 mm long, then either all blades less than 2 mm wide or the abaxial blade surfaces smooth or nearly so.
→ 9
9. Awns attached on the distal 2/5 of the lemmas, 0.5-2 mm long, straight; blades flat; panicles contracted, 0.7-2.5(3) cm wide.
→ 10
10. Lateral veins of the glumes prominent; rachillas hairy only distally
C. cinnoides
10. Lateral veins of the glumes obscure; rachillas hairy throughout their length
C. scopulorum
9. Awns attached on the lower 1/2(7/10) of the lemmas, 0.9-6 mm long, straight or bent; blades flat or involute; panicles open or contracted, 0.4-5.5(9) cm wide.
→ 11
11. Blades 0.2-1.7 mm wide; panicles (1.5)1.9-8.5 cm long; callus hairs sparse.
→ 12
12. Blades involute, 0.2-0.4 mm in diameter; ligules 1-2.5 mm long
C. muiriana
12. Blades flat, 0.9-1.7 mm wide, sometimes involute and 0.4-0.6 mm in diameter when dry; ligules 1.7-6 mm long
C. breweri
11. Blades (1)1.5-20 mm wide, most wider than 2 mm; panicles (2)3-30(40) cm long; callus hairs sparse to abundant.
→ 13
13. Awns usually exserted, (2.8)3-6 mm long; callus hairs 0.1-0.7 times as long as the lemmas; leaf collars hairy or glabrous.
→ 14
14. Culms 10-55(60) cm tall; panicles open; blades (1)1.5-3(4) mm wide.
→ 15
15. Blades 2-8(15) cm long; panicles erect; plants of brackish arctic and subarctic coastal habitats
C. deschampsioides
15. Blades (5)15-39 cm long; panicles often drooping; plants of rocky soils and disturbed sites in the mountains of Tennessee and North Carolina
C. cainii
14. Culms (26)50-210 cm tall; panicles open or contracted; blades (1)1.5-8(12) mm wide, most blades wider than 3 mm.
→ 16
16. Panicles open, 2.5-6 cm wide; panicle branches with the spikelets confined to the distal 1/4-1/2; leaf collars glabrous
C. bolanderi
16. Panicles usually contracted, 0.7-3(7) cm wide; panicle branches usually with the spikelets confined to the distal 1/2 - 2/3, sometimes spikelet-bearing to the base; leaf collars hairy or glabrous.
→ 17
17. Culms 135-210 cm tall; plants cultivated ornamentals
C. ×acutiflora
17. Culms 26-120 cm tall; plants native.
→ 18
18. Awns 4-5.5 mm long; leaf collars glabrous; plants often densely cespitose; rhizomes usually 2-4 mm thick
C. koelerioides
18. Awns 2-4.5 mm long; leaf collars sometimes hairy; plants loosely cespitose; rhizomes 0.5-2 mm thick.
→ 19
19. Blades (2)3-8(12) mm wide; panicle branches usually with the spikelets restricted to the distal 1/2 - 2/3, sometimes spikelet-bearing to the base; plants from east of the 100th meridian
C. porteri
19. Blades (1)2-5(8) mm wide; panicle branches spikelet-bearing to the base; plants from west of the 100th meridian
C. rubescens
13. Awns usually not exserted, or if exserted, then barely so, 0.9-3.1(4) mm long; callus hairs (0.1)0.2-1.2(1.5) times as long as the lemmas; leaf collars glabrous or hairy, if hairy, then the callus hairs more than 0.7 times as long as the lemmas.
→ 20
20. Callus hairs shorter than 1 mm, 0.2-0.3 times as long as the lemmas; awns bent
C. pickeringii
20. Callus hairs longer than 1 mm, (0.2)0.3-1.2(1.5) times as long as the lemmas; awns straight or bent.
→ 21
21. Culms usually scabrous, rarely smooth; awns slightly bent; callus hairs 0.4-0.8 times as long as the lemmas; blades usually involute, 1-4 mm wide, the abaxial surfaces scabrous; nodes 1-2
C. montanensis
21. Culms smooth to slightly scabrous; awns usually straight, rarely bent; callus hairs (0.2)0.5-1.2(1.5) times as long as the lemmas; blades flat or involute, 1-20 mm wide, the abaxial surfaces smooth or scabrous; nodes 1-8.
→ 22
22. Lemmas (3)4-5 mm long; glumes keeled; blades flat
C. nutkaensis
22. Lemmas 2-4(5) mm long, if the lemmas longer than 4 mm, then the glumes rounded and the abaxial blade surfaces smooth; glumes keeled or rounded; blades flat or involute.
→ 23
23. Panicle branches 2.7-6.5(12) cm long; ligules lacerate; glumes scabrous on the keels, often throughout; blades flat, the abaxial surfaces scabridulous or scabrous; nodes (2)3-7(8); panicles open.
→ 24
24. Awns bent, stout, readily distinguished from the callus hairs; collars densely hairy; plants of New York State
C. perplexa
24. Awns usually straight, delicate, often difficult to distinguish from the callus hairs; collars rarely hairy; plants of northern and western North America
C. canadensis
23. Panicle branches (1)1.4-5(9.5) cm long; if the panicle branches longer than 3.7 cm, then the ligules usually entire; glumes smooth or scabrous only on the keels; blades flat or involute, the abaxial surfaces smooth or scabrous; nodes 1-3(4); panicles loosely contracted.
→ 25
25. Glume lengths usually more than 3 times the widths, smooth, the keels rarely slightly scabrous, the lateral veins obscure; spikelets 3.5-5.5 mm long; awns usually slender and similar to the callus hairs
C. lapponica
25. Glume lengths usually less than 3 times the widths, usually smooth, rarely scabrous, the keels smooth or scabrous, the lateral veins prominent or obscure; spikelets 2-5 mm long; awns stout, usually readily distinguished from the callus hairs
C. stricta
Source FNA vol. 24. FNA vol. 24, p. 706. Author: Kendrick L. Marr; Richard J. Hebda; Craig W. Greenef;.
Parent taxa Poaceae > subfam. Pooideae > tribe Poeae > Calamagrostis Poaceae > subfam. Pooideae > tribe Poeae
Sibling taxa
C. bolanderi, C. breweri, C. cainii, C. canadensis, C. cinnoides, C. deschampsioides, C. epigejos, C. foliosa, C. howellii, C. koelerioides, C. lapponica, C. montanensis, C. muiriana, C. nutkaensis, C. ophitidis, C. perplexa, C. pickeringii, C. porteri, C. purpurascens, C. scopulorum, C. sesquiflora, C. stricta, C. tacomensis, C. tweedyi, C. ×acutiflora
Subordinate taxa
C. bolanderi, C. breweri, C. cainii, C. canadensis, C. cinnoides, C. deschampsioides, C. epigejos, C. foliosa, C. howellii, C. koelerioides, C. lapponica, C. montanensis, C. muiriana, C. nutkaensis, C. ophitidis, C. perplexa, C. pickeringii, C. porteri, C. purpurascens, C. rubescens, C. scopulorum, C. sesquiflora, C. stricta, C. tacomensis, C. tweedyi, C. ×acutiflora
Name authority Buckley Adans.
Web links