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

long-style thistle

Habit Biennials or perennials, 30–250 cm; taprooted. Perennials monocarpic, 40–150 cm; taprooted.
Stems

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

branches 0–many, ascending to spreading.

usually 1, erect, less commonly several, ascending, simple to sparingly short-branched in distal 1/2, less commonly openly branched, villous with jointed trichomes;

branches on distal stems 0–many, short, 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 linear to oblong or elliptic, 10–30+ × 1–10 cm, margins flat to undulate, subentire to coarsely dentate or shallowly to deeply pinnatifid, lobes lance-oblong to broadly triangular, spinulose to spiny-dentate or shallowly lobed, main spines 3–12 mm, abaxial faces green and subglabrous to gray- or white-tomentose with felted arachnoid trichomes, ± villous to tomentose along major veins with septate trichomes, rarely glabrous or glabrate, adaxial ± green, glabrous or villous with septate trichomes;

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

principal cauline well distributed, proximally winged-petiolate, distally sessile, gradually reduced, bases sometimes short-decurrent (0–2 cm);

distal ± reduced, often narrower than the proximal, sometimes with non-pigmented bases.

Peduncles

0–15 cm.

0–15+ cm.

Involucres

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

(green), broadly ovoid, 1.5–2.5 × 1.5–2.5 cm, loosely villous with septate trichomes, sparingly if at all arachnoid.

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, ochroleucous, 19–23 mm, tubes 6.5–8.5 mm, throats 7.5–11 mm, lobes 4–5 mm;

style tips 4–5.5 mm, conspicuously exserted.

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 4–8 series, subequal, ± lanceolate, bases appressed, apices ascending, linear to broadly expanded, erose to lacerate or spiny-fringed, spines straight, slender, 2–3 mm, abaxial faces with or without narrow glutinous ridge;

apices of inner flexuous, sometimes expanded and erose.

Heads

1–many, in corymbiform or paniculiform arrays.

several–many, erect, usually in racemiform or spiciform arrays, usually closely subtended by clustered ± leafy bracts.

Cypselae

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

pappi 14–16 mm.

brown, 5.5–6.5 mm, apical collars not differentiated;

pappi 17–20 mm.

2n

= 30, 32.

= 34.

Cirsium mohavense

Cirsium longistylum

Phenology Flowering summer–fall (Jun–Oct). Flowering summer (Jun–Aug).
Habitat Wet soil, streams, springs, meadows in desert and desert woodland areas Moist soil, roadsides, meadows, forest edges and openings
Elevation -50–2200 m (-200–7200 ft) 1500–2400 m (4900–7900 ft)
Distribution
from FNA
AZ; CA; NV; UT
[WildflowerSearch map]
[BONAP county map]
from FNA
MT
[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.)

Of conservation concern.

Cirsium longistylum is endemic to the Big Belt, Castle, Elkhorn, and Little Belt ranges of west-central Montana. It is highly variable, and several authors have suggested that it has introgressed with one or more other species (R. J. Moore and C. Frankton 1963; J. M. Poole and B. L. Heidel 1993; S. J. Brunsfeld and C. T. Baldwin, unpubl.). It is closely related to C. hookerianum, and the two probably share a common ancestry or a history of hybrid interactions dating back to the Pleistocene. Cirsium longistylum is perhaps also affected by modern or historic introgression involving C. scariosum var. scariosum.

(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. 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
Synonyms Carduus mohavensis, C. rusbyi, C. virginense
Name authority (Greene) Petrak: Bot. Tidsskr. 31: 68. (1911) R. J. Moore & Frankton: Canad. J. Bot. 41: 1562, plate 1. (1963)
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