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Mohave thistle, Mojave thistle, Rusby's thistle, virgin thistle

Parry thistle, Parry's thistle

Habit Biennials or perennials, 30–250 cm; taprooted. Biennials, 50–200+ cm; taprooted.
Stems

1–several, erect, proximally simple, distally branched, ± densely gray-tomentose;

branches 0–many, ascending to spreading.

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

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

Leaves

blades oblong-elliptic to oblanceolate, 10–60 × 2–15 cm, unlobed and merely spinulose or spiny-dentate or shallowly to deeply pinnatifid, lobes linear-lanceolate to ovate-triangular, spreading, entire to coarsely dentate, main spines slender to stout, 3–30 mm, faces ± gray-tomentose, sometimes ± glabrate;

basal often present at flowering, winged-petiolate;

principal cauline decreasing distally, proximal winged-petiolate, distal sessile, bases decurrent as spiny wings 1–5 cm;

distalmost well separated, bractlike.

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

0–15 cm.

0–4 cm.

Involucres

ovoid to hemispheric, 1.5–2.5 × 1.5–2 cm, loosely arachnoid on phyllary margins or glabrate.

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.

Corollas

white to pink or lavender, 16–25 mm, tubes 7–12 mm, throats 4–7 mm, lobes 4–8 mm, style tips 3–4 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 5–8 series, imbricate, (inner greenish to brown or stramineous), lanceolate or ovate (outer) to linear-lanceolate (inner), entire, abaxial faces with narrow glutinous ridge;

outer and middle appressed, spines spreading, 3–7 mm;

apices of inner often flexuous, flattened, spineless, scabrid.

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.

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

stramineous to dark brown, 3–6 mm, apical collars 0.2–0.3 mm, yellowish;

pappi 14–16 mm.

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

pappi 9–15 mm.

2n

= 30, 32.

= 34.

Cirsium mohavense

Cirsium parryi

Phenology Flowering summer–fall (Jun–Oct). Flowering summer–fall (Jul–Oct).
Habitat Wet soil, streams, springs, meadows in desert and desert woodland areas Stream banks, montane meadows, damp soil in montane coniferous forests
Elevation -50–2200 m (-200–7200 ft) 2100–3700 m (6900–12100 ft)
Distribution
from FNA
AZ; CA; NV; UT
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; CO; NM
[WildflowerSearch map]
[BONAP county map]
Discussion

Of conservation concern.

Cirsium mohavense ranges from scattered sites in eastern California east in the Basin and Range Province of southern Nevada to southwestern Utah and nortwestern Arizona, mostly in Mojave Desert region. When Welsh proposed Cirsium virginense for a geographically limited group of plants from southwestern Utah and northwestern Arizona (and subsequently discovered in extreme southeastern Nevada), he indicated that its relationship to other western thistles was unknown. Subsequently, he indicated (S. L. Welsh 1983; Welsh et al. 1993) that the affinities of the taxon apparently lie with C. mohavense, but he did not attempt to distinguish C. virginense from C. mohavense (in the strict sense) because the latter was not known to occur in Utah. A. Cronquist (1994) attempted the distinction. The only character he used in his key was life span of the plants: biennial (C. mohavense) versus perennial, spreading by creeping roots (C. virginense). In the descriptions of the two taxa he elaborated on this character, indicating that C. mohavense is single-stemmed and C. virginense often multistemmed. In the remaining features the plants are very similar or overlap extensively.

Distinction of two taxa on the basis of duration is impractical and probably inaccurate. Specimens commonly lack roots, and in those specimens in which bases are present, I have seldom been able to make any distinction between biennial taproots and perennial taproots. In particular I have seen no evidence of creeping roots. I am not aware of any study of either taxon that documents the life history of the plants. Some specimens of C. mohavense (in the strict sense) appear to have perennial bases like those attributed to C. virginense by Cronquist. For instance, a specimen of C. mohavense from Death Valley (Thorne & Ratcliff 2287, BRY) is indistinguishable from specimens of C. virginense (e.g., Atwood 13374, BRY) from Nevada and Utah. Both have a branched root crown with multiple rosettes and nearly identical leaves and heads.

(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. 134. FNA vol. 19, p. 149.
Parent taxa Asteraceae > tribe Cardueae > Cirsium Asteraceae > tribe Cardueae > Cirsium
Sibling taxa
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. 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 mohavensis, C. rusbyi, C. virginense Cnicus parryi, C. gilense, C. inornatum, C. pallidum, C. parryi subsp. mogollonicum
Name authority (Greene) Petrak: Bot. Tidsskr. 31: 68. (1911) (A. Gray) Petrak: Bot. Tidsskr. 31: 68. (1911)
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