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

roadside thistle, tall thistle

Parry thistle, Parry's 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, 50–200+ cm; taprooted.
Stems

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

branches few–many, ascending.

1, erect, puberulent to pilose with jointed trichomes, sometimes also thinly arachnoid;

branches 0–many, ascending, often nodding at tips.

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 lanceolate or oblanceolate, 10–30 × 2–5 cm, margins flat to undulate, spinulose and otherwise entire to coarsely dentate or shallowly to deeply pinnatifid, lobes well separated, spinulose to coarsely few-dentate, main spines slender to stout, 1–15 mm, one or both faces thinly pilose, sometimes thinly arachnoid, green and ± glabrescent at maturity;

basal usually absent at flowering, sessile or winged-petiolate;

principal cauline well distributed, proximal absent at flowering, moderately reduced distally, winged-petiolate or sessile (proximal), sessile and auriculate-clasping to slightly decurrent 0–2 cm;

distal well developed, spreading, lobed or unlobed.

Peduncles

0–5 cm (leafy-bracted).

0–4 cm.

Involucres

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

hemispheric to subspheric, 1.5–2.5 × 1.5–3 cm, glabrous to finely arachnoid and/or pilose, often long pilose-ciliate with arachnoid trichomes connecting adjacent phyllaries.

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.

ochroleucous to ± yellow (rarely white or purple), 11–17 mm, tubes 5.5–11 mm, throats 2–4 mm, lobes 3–5 mm;

style tips 2–4 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 5–8 series, imbricate to subequal, proximally greenish, distally darker, becoming brownish, linear to narrowly lanceolate, outer often nearly as long as inner, abaxial faces with poorly developed glutinous ridge;

outer and mid bases appressed, apices loosely ascending to spreading, bodies entire to spiny-ciliate or terminal appendages expanded, ± scarious, pectinately fringed, spines straight, 2–6 mm;

apices of inner flat or spine-tipped, sometimes expanded and fimbriate.

Heads

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

1–many, ± erect, loosely to densely clustered at tip of main stem and branches in subcapitate to racemiform arrays, often also in distal leaf axils, closely subtended by clusters of unlobed to deeply dissected, often very spiny bracts.

Cypselae

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

pappi 12–24 mm.

tan to dark brown, 4–6 mm, apical collars narrow, not differently colored;

pappi 9–15 mm.

2n

= 18.

= 34.

Cirsium altissimum

Cirsium parryi

Phenology Flowering summer–fall (Jun–Oct). Flowering summer–fall (Jul–Oct).
Habitat Prairies, woodlands, disturbed sites, often in damp soil Stream banks, montane meadows, damp soil in montane coniferous forests
Elevation 50–700 m (200–2300 ft) 2100–3700 m (6900–12100 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
AZ; CO; NM
[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 parryi ranges from the Rocky Mountains of central and southern Colorado south to the San Francisco Peaks, Pinaleno Mountains, and White Mountains of Arizona, and the Mogollon and Sacramento ranges of southern New Mexico. Within this broad range several minor variants have been recognized at the species level. The features that supposedly distinguish C. gilense, C. inornatum, and C. pallidum vary widely and inconsistently through the range of the species. In like manner the characters used by Schaack and Goodwin to distinguish subsp. mogollonicum fall well within the variation of the species as a whole and do not seem adequate to separate subsp. mogollonicum from the rest of C. parryi at any taxonomic rank. Cirsium parryi hybridizes with C. grahamii in Arizona and C. canescens in Colorado.

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

Source FNA vol. 19, p. 111. FNA vol. 19, p. 149.
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. occidentale, C. ochrocentrum, C. ownbeyi, C. palustre, 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 Cnicus parryi, C. gilense, C. inornatum, C. pallidum, C. parryi subsp. mogollonicum
Name authority (Linnaeus) Sprengel: Syst. Veg. 3: 373. (1826) (A. Gray) Petrak: Bot. Tidsskr. 31: 68. (1911)
Web links