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

Beaumont thistle, yellowspine thistle

Habit Biennials or perennials, 30–250 cm; taprooted. Perennials, 30–90 cm; crown sprouts or runner roots producing adventitious buds.
Stems

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

branches 0–many, ascending to spreading.

1–20+, erect or ascending, densely gray-tomentose with non-septate trichomes;

branches 0 or few, usually in distal 1/2, ascending.

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 narrowly elliptic, 10–30 × 2–8 cm, strongly undulate, margins coarsely dentate or shallowly to deeply pinnatifid with 8–15 pairs of lobes 0.5–2 cm, often revolute, lobes ± triangular, closely spaced, spreading, spinose-dentate and cleft into 2–5 spine-tipped divisions, main spines 5–20 mm, yellowish, abaxial faces densely white-tomentose, adaxial thinly gray-tomentose;

basal usually present at flowering, winged-petiolate;

principal cauline sessile, progressively reduced distally, bases ± auriculate to long-decurrent as spiny wings;

distal cauline usually much reduced, less lobed.

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.

ovoid to hemispheric or broadly campanulate, 2.5–4.5 × 2.5–4.5 cm in first-formed heads, often smaller in later ones, loosely arachnoid on phyllary margins or glabrate.

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.

white or pale lavender to purple, pink, or red, 25–45 mm, tubes 8–25 mm, throats 6–17 mm, lobes 6–15 mm;

style tips 2–8 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 5–10 series, imbricate, ovate (outer) to linear-lanceolate (inner), margins entire, abaxial faces with narrow glutinous ridge;

outer and middle appressed, spines spreading, 3–12 mm;

apices of inner often flexuous, expanded and flat, scabrid-margined, sometimes erose, spineless.

Heads

1–many, in corymbiform or paniculiform arrays.

1–few, in leafy, ± corymbiform arrays.

Cypselae

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

pappi 14–16 mm.

light brown, sometimes with lighter or darker streaks, 6–9 mm, apical collars colored like the body, narrow;

pappi (white or tawny), 20–40 mm, usually noticeably shorter than corolla.

2n

= 30, 32.

= 30, 31, 32, 34.

Cirsium mohavense

Cirsium ochrocentrum

Phenology Flowering summer–fall (Jun–Oct).
Habitat Wet soil, streams, springs, meadows in desert and desert woodland areas
Elevation -50–2200 m (-200–7200 ft)
Distribution
from FNA
AZ; CA; NV; UT
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; CA; CO; KS; NE; NM; OK; SD; TX; UT; WY; n Mexico
[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.)

Varieties 2 (2 in the flora).

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

Key
1. Stems densely leafy, nodes crowded; leaves often long- decurrent; corollas white or pale lavender to purple
var. ochrocentrum
1. Stems leafy, nodes usually well separated; distal cauline leaves clasping, or if decurrent spiny wing usually less than 1 cm; corollas red, pink, or reddish purple (rarely white)
var. martinii
Source FNA vol. 19, p. 134. FNA vol. 19, p. 123.
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. 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. ochrocentrum var. martinii, C. ochrocentrum var. ochrocentrum
Synonyms Carduus mohavensis, C. rusbyi, C. virginense
Name authority (Greene) Petrak: Bot. Tidsskr. 31: 68. (1911) A. Gray: Mem. Amer. Acad. Arts, n. s. 4: 110. (1849)
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