Cirsium hookerianum |
Cirsium eatonii |
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Hooker's thistle, white thistle |
Eaton's thistle, mountaintop thistle, Peck's thistle, Steens Mountain thistle |
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Habit | Biennials or monocarpic (sometimes polycarpic?) perennials, 20–150 cm; taprooted. | Perennials, 10–150 cm; taprooted caudices. | ||||||||||||||||||||||||||||
Stems | usually 1 and erect, less commonly several and ascending, simple to sparingly short-branched in distal 1/2, variably villous with jointed trichomes, and/or finely arachnoid, or ± glabrate; branches on distal stems 0–many, short, ascending. |
1–several, (fleshy), erect or ascending, simple to sparingly branched in distal 1/2, sometimes openly branched, glabrous to villous or tomentose with septate trichomes, sometimes ± glabrate; branches on distal stems 0–many, ascending. |
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Leaves | blades linear-oblong to elliptic, 5–25 × 1–8 cm, subentire to coarsely dentate or deeply pinnatifid, lobes lance-oblong to broadly triangular, spinulose to spiny-dentate or shallowly lobed, main spines 2–10 mm, abaxial faces usually ± densely gray- or white-tomentose with felted arachnoid trichomes, ± villous to tomentose along major veins with septate trichomes, sometimes glabrous or glabrate, adaxial ± green, glabrous to thinly arachnoid, often ± villous or tomentose 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; distal ± reduced, often narrower than proximal, sometimes with non-pigmented bases, sometimes pectinately spiny. |
blades oblong, 10–30 × 1–5 cm, margins usually strongly undulate, unlobed and spiny-dentate or shallowly to deeply pinnatifid with 10–20 pairs of lobes, teeth or lobes closely spaced, often overlapping, lance-oblong to broadly triangular, deeply 3-lobed, ± spiny-dentate, main spines 2–12 mm, abaxial faces glabrous or villous with septate trichomes along midveins to densely arachnoid-tomentose, adaxial glabrous or villous with septate trichomes along midveins; basal often present at flowering, spiny winged-petiolate or sessile; principal cauline many, well distributed, proximally ± winged-petiolate, distally sessile, gradually reduced; distal not much reduced, often closely subtending heads. |
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Peduncles | 0–8+ cm. |
0–14+ cm. |
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Involucres | (green or often purplish), broadly ovoid, 2–3.3 × 1.5–4 cm, loosely to densely villous with septate trichomes to tomentose and/or arachnoid. |
green or suffused with dark purple, broadly ovoid to campanulate, 2–5 × 1.5–5 cm (appearing wider when pressed), loosely to densely villous or tomentose with septate trichomes and/or arachnoid-tomentose with finer, non-septate trichomes. |
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Corollas | white, ochroleucous, or occasionally pink, 20–28 mm, tubes 10–13 mm, throats 6.5–9 mm, lobes 5–7 mm; style tips 3–5.5 mm. |
ochroleucous or yellow to lavender, pink, or purple, 15–35 mm, tubes 3.5–10 mm, throats 5–14 mm, lobes (linear), 4–12.5 mm; style tips 3–6 mm, conspicuously exserted beyond corolla lobes. |
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Phyllaries | in 4–8 series, imbricate to subequal, bases short-appressed, entire, abaxial faces with or without narrow glutinous ridge, apices stiffly spreading to ascending, linear, long, plane, spines straight, slender, 3–5 mm; apices of inner flexuous, sometimes expanded and erose. |
in 4–5 series, subequal, bases short-appressed, abaxial faces without or with very narrow glutinous ridge, apices usually stiffly ascending to spreading, linear-acicular, tapering to spines 7–35 mm; outer usually pinnately spiny, sometimes entire; apices of inner straight, plane or spine-tipped. |
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Heads | 1–many, borne singly or crowded in spiciform, racemiform, subcapitate, or sometimes more openly branched corymbiform arrays. |
1–many, erect or nodding, closely subtended by spiny-fringed bracts, usually sessile or short-pedunculate and crowded in subcapitate, spiciform, or racemiform (less commonly in openly branched) arrays. |
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Cypselae | dark brown, 5–6.5 mm, apical collars not differentiated; pappi 18–22 mm. |
dark brown, 5.5–7 mm, apical collars stramineous or not differentiated; pappi 12–25 mm. |
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2n | = 34. |
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Cirsium hookerianum |
Cirsium eatonii |
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Phenology | Flowering summer (Jun–Sep). | |||||||||||||||||||||||||||||
Habitat | Moist soil, grasslands, aspen parkland, forest edges and openings, subalpine, alpine meadows | |||||||||||||||||||||||||||||
Elevation | 600–2900 m (2000–9500 ft) | |||||||||||||||||||||||||||||
Distribution |
ID; MT; WA; WY; AB; BC
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CO; ID; MT; NM; NV; OR; UT; WY; Rocky Mountains and high peaks of Great Basin desert region
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Discussion | Cirsium hookerianum occurs from the Canadian Coast Ranges of British Columbia east to the northern Cascade Range and the northern Rocky Mountains. The relationship between C. hookerianum, C. kelseyi, which I have tentatively included in C. hookerianum, and C. longistylum needs further investigation. A case could be made for including all three in an expanded concept of C. hookerianum, but more investigation of the variation patterns is needed before this is done. Certainly C. kelseyi is better treated within or as a close ally of C. hookerianum than in C. scariosum (var. scariosum), where R. J. Moore and C. Frankton (1974) synonymized it. Cirsium hookerianum is known to hybridize with C. undulatum. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Varieties 7 (7 in the flora). Cirsium eatonii is a polymorphic species widely distributed in a high elevation archipelago across the central Rocky Mountains and the Intermountain Region. During Pleistocene glacial episodes, the progenitors of this species complex undoubtedly occupied lower elevation sites and likely had more contiguous populations. Post-glacial isolation of these populations in allopatric high elevation sites has allowed them to differentiate to a greater or lesser extent. Prehistoric or recent introgressive hybridization with other thistle species probably has contributed to the diversification of the complex (R. J. Moore and C. Frankton 1965). Several of the races recognized here as varieties have been treated in the past as species (e.g., C. clokeyi, C. peckii). Their current geographic isolation and more or less distinctive features might support such recognition, but application of this approach across the complex would result in a proliferation of microspecies. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 19, p. 148. | FNA vol. 19. | ||||||||||||||||||||||||||||
Parent taxa | Asteraceae > tribe Cardueae > Cirsium | Asteraceae > tribe Cardueae > Cirsium | ||||||||||||||||||||||||||||
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Synonyms | C. kelseyi | Cnicus eatonii | ||||||||||||||||||||||||||||
Name authority | Nuttall: Trans. Amer. Philos. Soc., n. s. 7: 418. (1841) | (A. Gray) B. L. Robinson: Rhodora 13: 240. (1911) | ||||||||||||||||||||||||||||
Web links |