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roadside thistle, tall thistle

chardon mutique, dunce-nettle, horsetops, swamp 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. Biennials, 30–230 cm; taproots fleshy.
Stems

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

branches few–many, ascending.

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

branches few–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.

ovate to broadly elliptic or obovate, 15–55 × 4–20 cm, deeply pinnatifid, to 7/8 to midribs, lobes linear to lanceolate, acute to acuminate, irregularly few toothed or lobed, main spines 2–3 mm, abaxial faces thinly tomentose or glabrate, villous with septate trichomes on the veins, adaxial faces thinly pilose;

basal usually absent at flowering, petioles spiny-winged, bases tapered;

principal cauline petiolate or sessile, gradually reduced distally, bases sometimes ± clasping, not decurrent;

distal cauline bractlike with narrowly linear lobes, often spinier than the proximal.

Peduncles

0–5 cm (leafy-bracted).

0–15 cm (sometimes overtopped by distal cauline leaves, not subtended by involucre-like ring of bracts).

Involucres

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

ovoid to broadly cylindric or campanulate, 1.7–3 × 1–3 cm, arachnoid.

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.

lavender or purple (white), 16–32 mm, tubes 7–15 mm, throats 4.5–10 mm (noticeably wider than tubes), lobes 4–8 mm;

style tips 3.5–5 mm.

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.

in 8–12 series, strongly imbricate, dull green with darker subapical patch, ovate (outer) to linear-lanceolate (inner), abaxial faces with narrow glutinous ridge, outer and middle appressed, bodies minutely spinulose, apices obtuse to acute, spines erect (sometimes appearing as spreading in dry specimens), 0–0.5 mm;

apices of inner phyllaries straight or ± flexuous, flattened.

Heads

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

1–many in ± open corymbiform or paniculiform arrays.

Cypselae

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

pappi 12–24 mm.

dark brown, 4.5–5.5 mm, apical collars yellow, 0.3 mm;

pappi 12–20 mm.

2n

= 18.

= 20, 21, 22, 23, 30.

Cirsium altissimum

Cirsium muticum

Phenology Flowering summer–fall (Jun–Oct). Flowering summer (Jul–Sep).
Habitat Prairies, woodlands, disturbed sites, often in damp soil Wet soil in meadows, prairies, marshes, swamps, bogs, open woods
Elevation 50–700 m (200–2300 ft) 0–1500+ m (0–4900+ 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
AL; AR; CT; DE; FL; GA; IA; IL; IN; KY; LA; MA; MD; ME; MI; MN; MO; NC; ND; NH; NJ; NY; OH; OK; PA; RI; SC; TN; TX; VA; VT; WI; WV; MB; NB; NL; NS; ON; PE; QC; SK; SPM
[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 muticum is very widely distributed across the eastern half of North America from the prairies of southeastern Saskatchewan across southern Canada to Newfoundland and south in the United States from North Dakota and Maine to southeastern Texas and northern Florida. It is more common in the northern half of this range and extends from the coastal plain to the Appalachian highlands. The widely scattered populations in coastal lowlands in the southern United States may be relicts of the glacial distribution of the species.

Cirsium muticum is known to hybridize with C. discolor (discussed thereunder) and C. flodmanii. Draining and modification of wetlands have affected populations of C. muticum in some areas.

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

Source FNA vol. 19, p. 111. FNA vol. 19, p. 113.
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. 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. 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 Carduus muticus, C. muticum var. monticola
Name authority (Linnaeus) Sprengel: Syst. Veg. 3: 373. (1826) Michaux: Fl. Bor.-Amer. 2: 89. (1803)
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