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roadside thistle, tall thistle

desert or New Mexico thistle, desert thistle, New Mexico 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, 40–290 cm; taprooted.
Stems

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

branches few–many, ascending.

usually 1, erect, thinly gray-tomentose, sometimes ± glabrate;

branches few–many, usually from above middle, 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–elliptic to oblanceolate, 6–35 × 1.5–7 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, faces gray-tomentose, sometimes glabrate;

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

principal cauline sessile, much reduced distally, bases decurrent as spiny wings less than 5 cm;

distal much reduced, ± bractlike, sometimes scarcely more than a cluster of long spines.

Peduncles

0–5 cm (leafy-bracted).

(2.5–)5–30 cm, bracted.

Involucres

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

shallowly hemispheric or campanulate, 2–3 × 2.5–5 cm, arachnoid to ± loosely tomentose, sometimes glabrous.

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 pale lavender or pink, 18–27 mm, tubes 8–14 mm, throats 4–7 mm, lobes 5–9 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, imbricate to subequal, linear to narrowly lanceolate, abaxial faces with narrow or no glutinous ridge;

outer and mid bodies appressed, entire or minutely spinulose, apices deflexed to spreading or ascending, long, flat, spines spreading to reflexed, 4–15 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.

1–6 (many on large individuals), borne singly or in corymbiform arrays.

Cypselae

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

pappi 12–24 mm.

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

pappi 15–20 mm.

2n

= 18.

= 30 (as C. utahense), 32; 30 + 1 I.

Cirsium altissimum

Cirsium neomexicanum

Phenology Flowering summer–fall (Jun–Oct). Flowering spring–summer (Mar–Jul).
Habitat Prairies, woodlands, disturbed sites, often in damp soil Canyons, slopes, roadsides in deserts, dry grasslands, and arid woodlands dominated by pinyon pines, junipers, oaks, Joshua trees
Elevation 50–700 m (200–2300 ft) 300–2100 m (1000–6900 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
AZ; CA; CO; NM; NV; TX; UT; Mexico (Sonora)
[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.)

Desert thistle is widespread in the Mojave and Sonoran deserts and ranges into the southern Great Basin desert, western Chihuahuan desert, and into adjacent mountains of Utah, southwestern Colorado, Arizona, and New Mexico.

The name Cirsium utahense has been widely applied in the past to plants that are here recognized as C. inamoenum. S. L. Welsh (1983) treated it as a variety of C. neomexicanum. I have examined the type of C. utahense and can find no basis for distinguishing it from C. neomexicanum at any rank. The desert thistle is closely related to C. occidentale.

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

Source FNA vol. 19, p. 111. FNA vol. 19, p. 140.
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. 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 C. arcuum, C. humboldtense, C. neomexicanum var. utahense, C. undulatum var. albescens, C. utahense
Name authority (Linnaeus) Sprengel: Syst. Veg. 3: 373. (1826) A. Gray: Smithsonian Contr. Knowl. 5(6): 101. (1853)
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