Cirsium hookerianum |
Cirsium arizonicum |
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Hooker's thistle, white thistle |
Arizona thistle |
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Habit | Biennials or monocarpic (sometimes polycarpic?) perennials, 20–150 cm; taprooted. | Perennials, 30–150 cm; taprooted caudices or runner roots. | ||||||||||||||||
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, erect or ascending, glabrous to thinly arachnoid-tomentose with fine non-septate trichomes and/or villous with septate trichomes, sometimes ± glabrate; branches 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-elliptic, 3–40 × 1–13 cm, unlobed and spinulose to shallowly lobed or divided nearly to midvein, lobes few–many, ovate to linear-acuminate, often again lobed or divided, main spines 2–30 mm, abaxial faces green, glabrous to densely gray tomentose, sometimes midveins villous with septate trichomes, adaxial green, glabrous to gray-tomentose, sometimes glabrate; basal sometimes present at flowering, unlobed to deeply spiny-lobed, winged-petiolate or sessile; principal cauline sessile, well distributed, gradually diminished distally, bases sometimes decurrent as spiny wings to 2.5 cm or clasping; distalmost sometimes ± bractlike. |
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Peduncles | 0–8+ cm. |
0–15 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. |
cylindric or ovoid to campanulate, 1.5–4 × 1–2.5 cm (body), loosely arachnoid or ± glabrous. |
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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. |
pink to red, lavender, or purple (white), 25–31 mm, tubes 7–12.5 mm, throats 1.5–8.5 mm, lobes 10–17 mm; style tips 1–4 mm. |
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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 7–9 series, imbricate, green or the inner reddish to rich reddish purple, ovate or lanceolate (outer) to linear (inner), margins of outer entire, abaxial faces often with narrow, inconspicuous glutinous ridge; outer and mid bodies appressed, short, entire, apices spreading to ascending, inconspicuous to long, narrow, entire or minutely ciliolate, spines erect to reflexed (outer) to ascending (inner), slender to stout, cylindric or basally flattened, 1–30 mm; apices of inner unarmed or with straight or flexuous spines, short, flat. |
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Heads | 1–many, borne singly or crowded in spiciform, racemiform, subcapitate, or sometimes more openly branched corymbiform arrays. |
1–100+, erect, in corymbiform or paniculiform arrays. |
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Cypselae | dark brown, 5–6.5 mm, apical collars not differentiated; pappi 18–22 mm. |
brown, 3.5–7 mm, apical collars stramineous, 0.2–0.3 mm; pappi 17–28 mm. |
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2n | = 34. |
= 30, 32, 34. |
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Cirsium hookerianum |
Cirsium arizonicum |
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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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AZ; CA; CO; NM; NV; UT; nw Mexico
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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 5 (5 in the flora). The Cirsium arizonicum complex is widely distributed from the Sierra Nevada, White Mountains, and New York Mountains of eastern California across the mountains of the southern Great Basin and Colorado Plateau to the mountains of eastern Colorado, Arizona, and New Mexico. This group of plants comprises a series of intergrading races with intricately overlapping patterns of variation. For plants that I am treating as C. arizonicum (in the broad sense), F. Petrak (1917) recognized three species, one with a variety and two subspecies plus his unstated type subspecies and variety. R. J. Moore and C. Frankton (1974b) revised the complex, recognizing six species, three of them newly described, for the plants I treat as C. arizonicum plus C. turneri, which I do not include in C. arizonicum. P. L. Barlow-Irick (2002), in a work focused on statistical analyses of variation patterns, recognized six species also, but circumscribed very differently from those of Moore and Frankton. Two of the species proposed by Barlow-Irick have not been formally described. I have wrestled with how to treat these plants since beginning my research for this treatment. After careful consideration of the complex patterns of variation among members of the C. arizonicum complex, I acknowledged the futility of trying to distinguish more than one species. Any character combinations that I or others have attempted to use to distinguish species break down hopelessly when enough specimens are examined. Instead I have chosen to recognize that in this complex, as in several others, the plants in question are a work of evolution in progress. Cirsium arizonicum is a rapidly evolving, only partially differentiated assemblage of races that have not reached the level of stability that is usually associated with the concept of species. Certainly there is much variation within the group that deserves a level of taxonomic recognition, or at least should be mentioned, but I think it much more prudent to recognize varieties–entities that may be expected to freely intergrade–rather than species. The geographic area where these plants occur, the highlands of the American Southwest, has had a turbulent history in the Quaternary with major shifts in climate, vegetation, and elevational zonation accompanying the vicissitudes of glacial and interglacial episodes. The complicated patterns of variation in C. arizonicum reflect both that history and the geographic and topographic complexity of the region. Heads of Cirsium arizonicum are visited by hummingbirds as well as a variety of insects (P. L. Barlow-Irick 2002). Hummingbirds are the most common visitors, but hummingbirds and bees are both apparently effective pollinators in C. arizonicum. (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, p. 141. | ||||||||||||||||
Parent taxa | Asteraceae > tribe Cardueae > Cirsium | Asteraceae > tribe Cardueae > Cirsium | ||||||||||||||||
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Subordinate taxa | ||||||||||||||||||
Synonyms | C. kelseyi | Cnicus arizonicus | ||||||||||||||||
Name authority | Nuttall: Trans. Amer. Philos. Soc., n. s. 7: 418. (1841) | (A. Gray) Petrak: Bot. Tidsskr. 31: 68. (1911) | ||||||||||||||||
Web links |