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roadside thistle, tall thistle

cobwebby thistle, snowy thistle, Venus thistle, western 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, 5–400 cm; taproots.
Stems

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

branches few–many, ascending.

usually 1, thinly to densely gray- or white-tomentose, sometimes ± glabrate;

branches few–many, usually from above mid or near base in compact, moundlike dwarf plants, ascending to spreading.

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–elliptic to oblanceolate, 6–40 × 1.5–10+ cm, shallowly to deeply pinnatifid, lobes usually rigidly spreading, undivided or with 1–2 pairs of coarse teeth or lobes, main spines 5–15 mm, both faces gray- to white-tomentose, sometimes ± glabrate or adaxial faces green, thinly arachnoid-tomentose;

basal sometimes present at flowering, petiolate or sessile and bases tapered, spiny-winged;

principal cauline much reduced distally, sessile, bases decurrent or not, as spiny wings;

distal much reduced, linear, ± bractlike.

Peduncles

0–5 cm (leafy-bracted).

1–30 cm.

Involucres

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

ovoid to spheric, 1.5–5 × 1.5–8 cm, arachnoid to ± loosely tomentose, often adjacent phyllaries connected by conspicuous arachnoid trichomes, sometimes glabrous or glabrate.

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 lavender, pink, rose-purple, or red, 18–40 mm, tubes 8–18 mm, throats 5–7 mm, lobes 5–10 mm;

style tips 4–5 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 7–10 series, subequal to strongly imbricate, green or stramineous to purple-tinged, linear to narrowly lanceolate, abaxial faces without glutinous ridge;

outer and mid bodies appressed, entire, apices deflexed to spreading or ascending, short-triangular to elongate, linear-acicular, spines spreading to reflexed, 1–10+ mm;

apices of inner erect, often flexuous, flat.

Heads

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

1–many in loose to tight clusters (barely raised above rosette in dwarf plants).

Cypselae

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

pappi 12–24 mm.

± brown, 5–6 mm, apical collars not differentiated;

pappi 15–30 mm.

2n

= 18.

Cirsium altissimum

Cirsium occidentale

Phenology Flowering summer–fall (Jun–Oct).
Habitat Prairies, woodlands, disturbed sites, often in damp soil
Elevation 50–700 m (200–2300 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; NV; OR
[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.)

Varieties 7 (7 in the flora).

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

Key
1. Plants compact, rounded, moundlike; heads usually not much elevated above leaves
var. compactum
1. Plants usually erect; principal heads usually conspicuously pedunculate
→ 2
2. Corollas white to light purple or rose
var. californicum
2. Corollas deep purple to bright pink or red
→ 3
3. Plants densely white-tomentose; phyllaries persistently white-tomentose (except spines); outer phyllaries usually very long, spreading to reflexed
var. candidissimum
3. Plants variably tomentose, sometimes ± glabrate; phyllaries ± arachnoid to floccose-tomentose, sometimes green and glabrate; outer phyllaries short to long, ascending to spreading or reflexed
→ 4
4. Involucres usually about as long as wide or wider than long; phyllaries densely and persistently arachnoid with fine trichomes connecting tips of adjacent phyllaries
→ 5
4. Involucres usually longer than wide; phyllaries tomentose or glabrate, sparingly or not arachnoid with fine trichomes connecting tips of adjacent phyllaries
→ 6
5. Phyllary apices ± imbricate, the proximal usually shorter than medial and distal, lanceolate to linear-acicular, 0.5–15 mm; co- rollas bright purple
var. occidentale
5. Phyllary apices subequal, all long- acicular, 1.5–3 cm; corollas light to deep reddish purple
var. coulteri
6. Corollas 20–24 mm, deep reddish purple; s Santa Lucia Mountains of San Luis Obispo County, California
var. lucianum
6. Corollas 23–35 mm, bright pink to red; widespread
var. venustum
Source FNA vol. 19, p. 111. FNA vol. 19, p. 137.
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. muticum, C. neomexicanum, C. nuttallii, 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
Subordinate taxa
C. occidentale var. californicum, C. occidentale var. candidissimum, C. occidentale var. compactum, C. occidentale var. coulteri, C. occidentale var. lucianum, C. occidentale var. occidentale, C. occidentale var. venustum
Synonyms Carduus altissimus, C. altissimum var. biltmoreanum, C. iowense Carduus occidentalis
Name authority (Linnaeus) Sprengel: Syst. Veg. 3: 373. (1826) (Nuttall) Jepson: Fl. W. Calif., 509. (1901)
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