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roadside thistle, tall thistle

cluster thistle, Indian or cluster or short-style thistle, Indian thistle, short-style thistle

Habit Biennials or short-lived monocarpic perennials, (50–)100–300(–400) cm; taproots and often a cluster of coarse fibrous roots, roots without tuberlike enlargements. Annuals or biennials, 20–350 cm; taprooted.
Stems

single, erect, villous with septate trichomes, sometimes ± glabrate, sometimes distally thinly tomentose;

branches few–many, ascending.

usually 1, erect, simple or branched in distal 1/2, loosely to densely villous or viscid-pilose with jointed trichomes, often arachnoid below heads;

branches 0–many, ascending.

Leaves

blades oblanceolate to elliptic or ovate, 10–40 × 1–13 cm, margins flat, finely spiny-toothed and otherwise undivided to coarsely toothed or shallowly pinnatifid, lobes broadly triangular, main spines 1–5 mm, abaxial faces white-tomentose, adaxial faces green, glabrate to villous with septate trichomes;

basal usually absent at flowering, winged-petiolate, bases tapered;

principal cauline well distributed, gradually reduced, bases narrowed, sometimes weakly clasping;

distal cauline well developed.

blades oblong to elliptic or oblanceolate, 15–35 × 2–10 cm, flat to ± undulate, coarsely dentate to shallowly pinnatifid, lobes broadly triangular, spinulose to spiny-dentate or shallowly lobed, main spines slender, 3–7 mm, abaxial faces thinly gray-tomentose, villous along major veins, sometimes glabrescent, adaxial sparsely villous or viscid-pilose along midveins with jointed trichomes;

basal often absent at flowering, spiny winged-petiolate;

principal cauline well distributed, gradually reduced, proximal winged-petiolate, mid and distal sessile, bases clasping or short-decurrent;

distal moderately to strongly reduced, often spinier than the proximal.

Peduncles

0–5 cm (leafy-bracted).

0–1(–30) cm.

Involucres

ovoid to broadly cylindric or campanulate, (2–)2.5–3.5(–4) × (1.5–)2–3(–4) cm, thinly arachnoid.

hemispheric to campanulate, 2.5–3.5 cm, 2.5–4 cm diam., loosely to densely arachnoid, phyllaries connected by long septate or non-septate trichomes.

Style

tips 4–6 mm.

Corollas

pink to purple (white), 20–35 mm, tubes 10–16 mm, throats 5–12 mm, lobes 5–9 mm.

white to pink or purple, very slender, 20–25 mm, tubes 10–17 mm, throats 4–5 mm, lobes filiform with knoblike tips, 3–5 mm;

style tips 2–4 mm, included or exserted (only 1–2 mm beyond corolla lobes).

Phyllaries

in 10–20 series, strongly imbricate, greenish with subapical darker central zone, ovate (outer) to lanceolate (inner), abaxial faces with a narrow glutinous ridge (milky when fresh, dark when dry), outer and middle entire, bodies appressed, spines slender, abruptly spreading, 3–4 mm;

apices of inner phyllaries spreading, narrow, flattened, entire, spines spreading, slender, 3–4 mm;

apices of inner phyllaries spreading, narrow, flattened, ± dilated, ± erose or finely serrulate.

radiating in 5–10 series, subequal, green, linear-acicular, outermost margins sometimes spiny-fringed, otherwise all entire or minutely serrulate, abaxial faces without glutinous ridge;

outer and mid bases short-appressed, apices stiffly radiating to ascending, long, very narrow, spines straight, slender, 3–5 m;

apices of inner straight, flat.

Heads

1–many, in corymbiform or paniculiform arrays, (± elevated above principal cauline leaves), not subtended by ring of spiny bracts.

1–many, ± erect, usually crowded in subcapitate to tight corymbiform arrays, closely subtended by clustered ± leafy bracts.

Cypselae

tan to dark brown, 4–5.5 mm, apical collars stramineous, 0.5–1 mm;

pappi 12–24 mm.

brown, 3–4.5 mm, apical collars stramineous, 0.2 mm;

pappi 10–22 mm.

2n

= 18.

= 34.

Cirsium altissimum

Cirsium brevistylum

Phenology Flowering summer–fall (Jun–Oct). Flowering spring–summer (Apr–Sep).
Habitat Prairies, woodlands, disturbed sites, often in damp soil Coastal meadows, marshes, swamps, riparian woodlands, moist sites in coastal scrub, chaparral, coastal woodlands, mixed conifer-hardwood forests, or coniferous forests
Elevation 50–700 m (200–2300 ft) 0–1000 m (0–3300 ft)
Distribution
from FNA
AL; AR; DC; DE; FL; GA; IA; IL; IN; KS; KY; LA; MA; MD; MI; MN; MO; MS; NC; ND; NE; NY; OH; OK; PA; SC; SD; TN; TX; WI; WV
[WildflowerSearch map]
[BONAP county map]
from FNA
CA; ID; MT; OR; WA; BC
[WildflowerSearch map]
[BONAP county map]
Discussion

Plants of Cirsium altissimum ranging from southern Minnesota to Texas often have more deeply divided leaves than do populations in other portions of the species’ range. Some botanists (e.g., R. J. Moore and C. Frankton 1969; D. S. Correll and M. C. Johnston 1970) have treated those plants as C. iowense. Others (e.g., R. E. Brooks 1986; H. A. Gleason and A. Cronquist 1991; G. B. Ownbey and T. Morley 1991) have treated them as C. altissimum. Still others considered them to be derivatives of hybridization between C. altissimum and C. discolor (J. T. Kartesz and C. A. Meacham 1999) and treated them as C. ×iowense. Indeed the existence of these plants blurs the distinction between C. altissimum and C. discolor, and herbarium specimens are often difficult to assign.

Natural hybrids between Cirsium altissimum and C. discolor are well documented (R. A. Davidson 1963; G. B. Ownbey and Hsi Y.-T. 1963; Ownbey 1964; S. Dabydeen 1997). Ownbey and Dabydeen both reported that apparent F1 hybrids between the two species have low seed set in comparison with the parental taxa. W. L. Bloom (1977) reported that the chromosomes of the two species differ by several rearareaments. Dabydeen reported a count of 2n = 19 with multiple meiotic irregularities for an apparent F1 hybrid. However, the presence of numerous individuals and populations seemingly intermediate between C. altissimum and C. discolor indicates that although F1 hybrids have low fertility, long-term processes may have stabilized hybrid derivatives of higher fertility. Ownbey and Hsi reported mitotic counts of 2n = 18 and 20 from a population that they treated as C. altissimum. In their discussion they noted that their plants represented “the segregate called C. iowense” and had been collected a short distance from that taxon’s type locality. R. J. Moore and C. Frankton (1969) reported a chromosome number of 2n = 18 for a plant from Texas that they considered to be C. iowense. Further investigation of morphologic variation, chromosome number, meiotic behavior, and fertility is needed of populations named as C. iowense to determine how those plants should be treated.

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

Cirsium brevistylum occurs in the coast ranges and adjacent coastal slope from southwestern British Columbia to southern California. In the Pacific Northwest its range extends inland to the northern Rocky Mountains of southern British Columbia, Idaho, and northwestern Montana, and the Blue and Wallowa ranges of eastern Oregon. It is absent from the central and southern Cascade Range.

In older literature the name Cirsium edule was widely misapplied to this species. A. Cronquist (1953) pointed out that the type of C. edule has corolla and style features quite different from those of the plants that had been called by that name and established the name C. brevistylum, based upon the notably short styles of this species. Hybrids of C. brevistylum with C. edule have been named C. ×vancouveriense R. J. Moore & C. Frankton.

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

Source FNA vol. 19, p. 111. FNA vol. 19, p. 148.
Parent taxa Asteraceae > tribe Cardueae > Cirsium Asteraceae > tribe Cardueae > Cirsium
Sibling taxa
C. andersonii, C. andrewsii, C. arizonicum, C. arvense, C. barnebyi, C. brevifolium, C. brevistylum, C. canescens, C. carolinianum, C. ciliolatum, C. clavatum, C. crassicaule, C. cymosum, C. discolor, C. douglasii, C. drummondii, C. eatonii, C. edule, C. engelmannii, C. flodmanii, C. foliosum, C. fontinale, C. grahamii, C. helenioides, C. hookerianum, C. horridulum, C. hydrophilum, C. inamoenum, C. joannae, C. kamtschaticum, C. lecontei, C. longistylum, C. mohavense, C. muticum, C. neomexicanum, C. nuttallii, C. occidentale, C. ochrocentrum, C. ownbeyi, C. palustre, C. parryi, C. perplexans, C. pitcheri, C. praeteriens, C. pulcherrimum, C. pumilum, C. quercetorum, C. remotifolium, C. repandum, C. rhothophilum, C. rydbergii, C. scariosum, C. texanum, C. tracyi, C. turneri, C. undulatum, C. vinaceum, C. virginianum, C. vulgare, C. wheeleri, C. wrightii
C. altissimum, C. andersonii, C. andrewsii, C. arizonicum, C. arvense, C. barnebyi, C. brevifolium, C. canescens, C. carolinianum, C. ciliolatum, C. clavatum, C. crassicaule, C. cymosum, C. discolor, C. douglasii, C. drummondii, C. eatonii, C. edule, C. engelmannii, C. flodmanii, C. foliosum, C. fontinale, C. grahamii, C. helenioides, C. hookerianum, C. horridulum, C. hydrophilum, C. inamoenum, C. joannae, C. kamtschaticum, C. lecontei, C. longistylum, C. mohavense, C. muticum, C. neomexicanum, C. nuttallii, C. occidentale, C. ochrocentrum, C. ownbeyi, C. palustre, C. parryi, C. perplexans, C. pitcheri, C. praeteriens, C. pulcherrimum, C. pumilum, C. quercetorum, C. remotifolium, C. repandum, C. rhothophilum, C. rydbergii, C. scariosum, C. texanum, C. tracyi, C. turneri, C. undulatum, C. vinaceum, C. virginianum, C. vulgare, C. wheeleri, C. wrightii
Synonyms Carduus altissimus, C. altissimum var. biltmoreanum, C. iowense
Name authority (Linnaeus) Sprengel: Syst. Veg. 3: 373. (1826) Cronquist: Leafl. W. Bot. 7: 26. (1953)
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