Cirsium palustre |
Cirsium arizonicum |
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cirse ou chardon des marais, European Marsh thistle, European swamp or marsh thistle, European swamp thistle, marsh thistle |
Arizona thistle |
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Habit | Biennials or monocarpic perennials, 30–200(–300) cm; clusters of fibrous roots. | Perennials, 30–150 cm; taprooted caudices or runner roots. | ||||||||||||||||
Stems | single, erect, villous to tomentose with jointed trichomes, distally tomentose with fine, unbranched trichomes; branches 0–few, ascending, (short). |
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 narrowly elliptic to oblanceolate, 15–30+ × 3–10 cm, margins shallowly to very deeply pinnatifid, narrow lobes separated by broad sinuses, spiny-dentate to lobed, main spines 2–6 mm, abaxial villous to tomentose with jointed trichomes, sometimes also thinly tomentose with fine unbranched trichomes, adaxial faces villous with septate trichomes or glabrate; basal often present at flowering, petioles spiny-winged, bases tapered; cauline many, sessile, gradually reduced and becoming widely spaced above, bases long-decurrent with prominently spiny wings; distal cauline deeply pinnatifid with few-toothed spine-tipped lobes. |
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 | 0–1 cm. |
0–15 cm. |
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Involucres | ovoid to campanulate, 1–1.5 × 0.8–1.3 cm, thinly cobwebby tomentose with fine unbranched trichomes. |
cylindric or ovoid to campanulate, 1.5–4 × 1–2.5 cm (body), loosely arachnoid or ± glabrous. |
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Corollas | lavender to purple (white), 11–13 mm, tubes 5–7 mm, throats 2–3 mm, lobes 3–4.5 mm; style tips 1.5–2 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 5–7 series, strongly imbricate, greenish, or with purplish tinge, lanceolate to ovate (outer) or linear-lanceolate (inner), margins thinly arachnoid-ciliate, abaxial faces with narrow glutinous ridge, outer and middle appressed, entire, apices acute, mucronate or spines erect or spreading, weak, 0.3–1 mm; apices of inner phyllaries purplish, linear-attenuate, scarious, flat. |
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 | few–many in dense clusters at branch tips. |
1–100+, erect, in corymbiform or paniculiform arrays. |
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Cypselae | tan to stramineous, 2.5–3.5 mm, apical collars 0.1–0.2 mm, shiny; pappi 9–11 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 palustre |
Cirsium arizonicum |
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Phenology | Flowering summer (Jul–Aug). | |||||||||||||||||
Habitat | Marshes, wet forests | |||||||||||||||||
Elevation | 10–800 m (0–2600 ft) | |||||||||||||||||
Distribution |
MA; MI; NH; NY; WI; BC; NF; NS; ON; QC; SPM; Europe [Introduced in North America]
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AZ; CA; CO; NM; NV; UT; nw Mexico
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Discussion | Cirsium palustre is a noxious weed, native to Europe, that invasively spreads through wetland communities, forming impenetrable spiny stands as it displaces native species. The range of this pernicious weed in North America is rapidly expanding. It has the potential to spread into boreal forest areas across the continent; in Europe it grows nearly to the Arctic Circle. The rapid spread of C. palustre in Michigan (E. G. Voss 1972–1996, vol. 3) is indicative of its invasiveness. Spontaneous hybrids between C. palustre and C. arvense have been reported from England and other European countries (W. A. Sledge 1975) and can be expected wherever these species grow together in North America. (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. 110. | FNA vol. 19, p. 141. | ||||||||||||||||
Parent taxa | Asteraceae > tribe Cardueae > Cirsium | Asteraceae > tribe Cardueae > Cirsium | ||||||||||||||||
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Subordinate taxa | ||||||||||||||||||
Synonyms | Carduus palustris | Cnicus arizonicus | ||||||||||||||||
Name authority | (Linnaeus) Scopoli: Fl. Carniol. ed. 2, 2: 128. (1772) | (A. Gray) Petrak: Bot. Tidsskr. 31: 68. (1911) | ||||||||||||||||
Web links |