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roadside thistle, tall thistle

Adobe Hills thistle, Rocky Mountain 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, slender, 20–100 cm; taprooted.
Stems

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

branches few–many, ascending.

usually 1, erect, thinly arachnoid-tomentose, sparsely pilose distally with short, jointed trichomes;

branches few to many, often arising from proximal nodes, 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, 15–30 × 2–6 cm, often unlobed and merely spinulose or spiny-dentate, sometimes pinnatifid ca. halfway to midveins, lobes separated by broad sinuses, undivided to coarsely few-dentate, main spines slender, 2–5(–10) mm, abaxial faces ± persistently thinly gray-tomentose, adaxial green, glabrous to thinly tomentose, sometimes sparsely pilose on midveins;

basal sometimes present at flowering, sessile or short winged-petiolate;

principal cauline sessile, progressively reduced, becoming bractlike distally, mid and distal bases broadly clasping;

distal reduced to linear or lanceolate bracts.

Peduncles

0–5 cm (leafy-bracted).

(0–)3–20 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, 1.3–2.5 × (1–)1.5–2.5 cm, glabrous to loosely floccose.

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 to reddish purple, (16–)19–22 mm, tubes 6–9 mm, throats 5–8 mm, lobes 5–7 mm, style tips 5–6 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(–10) series, strongly imbricate, green with darker green to brown subapical patch, broadly ovate or oblong (outer) to lanceolate (inner), abaxial faces with prominent to obscure glutinous ridge;

outer and middle appressed, spines or terminal appendages spreading to reflexed, bodies entire or with expanded, ± scarious, ± pectinately fringed terminal appendages, tips merely mucronate or with weak spines spreading to reflexed, 1–3 mm;

apices of inner often flexuous, flat, scarious, serrulate to expanded and pectinately fringed.

Heads

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

few–many, in ± openly branched corymbiform or paniculiform arrays;

not 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.

dark brown, 4–5 mm, apical collars stramineous or not differently colored, very narrow;

pappi 15–17 mm.

2n

= 18.

Cirsium altissimum

Cirsium perplexans

Phenology Flowering summer–fall (Jun–Oct). Flowering spring–summer (May–Aug).
Habitat Prairies, woodlands, disturbed sites, often in damp soil Barren shale hillsides, gypsiferous clay soils, open, nearly unvegetated sites in areas of pinyon-juniper woodlands, sagebrush scrub, saltbush scrub, or Gambel oak brush, roadsides
Elevation 50–700 m (200–2300 ft) 1800–2100 m (5900–6900 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
CO
[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 perplexans occurs in a few scattered sites at relatively low elevations in the Rocky Mountains of west-central Colorado. In view of this restricted distribution, the common name used by governmental agencies, Rocky Mountain thistle, is misleading; one would expect a species so named to be widely distributed in the Rocky Mountains. The name Adobe Hills thistle is descriptive of the habitat.

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

Source FNA vol. 19, p. 111. FNA vol. 19, p. 128.
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. parryi, 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 perplexans, C. vernale
Name authority (Linnaeus) Sprengel: Syst. Veg. 3: 373. (1826) (Rydberg) Petrak: Beih. Bot. Centralbl. 35(2): 441. (1917)
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