Cirsium scariosum |
Asteraceae tribe Cardueae |
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chardon écailleux, dinnerplate thistle, elk thistle, meadow thistle |
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Habit | Biennials or monocarpic perennials, acaulescent, short caulescent and forming low rounded mounds, or caulescent and erect, 0–200 cm; taprooted. | Annuals or perennials (sometimes coarse and/or robust, often prickly-spiny and thistlelike [subshrubs, shrubs, or trees]; rarely dioecious, e.g., some Cirsium spp.). | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stems | absent, or with crowded branches from near base, or simple and erect, often fleshy and thickened, glabrous to thinly gray- tomentose, often villous with septate trichomes. |
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Leaves | blades linear to elliptic, 5–20 × 3–7 cm, plane to strongly undulate, unlobed or shallowly to deeply pinnatifid, lobes linear-lanceolate to broadly triangular, closely spaced, spreading, spinose-dentate or lobed, main spines slender to stout, 2–15+ mm, abaxial faces glabrous or thinly to densely tomentose, ± villous with septate trichomes along the veins, glabrate or trichomes persistent, adaxial thinly arachnoid tomentose and soon glabrescent; basal often present at flowering, sessile or winged-petiolate; cauline many in caulescent forms, reduced distally or not, winged-petiolate or distal sessile; distal often well developed, similar to proximal, sometimes much narrower and bractlike. |
basal and/or cauline; alternate; ± petiolate or sessile; (leaf bases often decurrent on stems) margins usually lobed to dissected, sometimes dentate or entire (usually spiny). |
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Peduncles | 0–10 cm, leafy-bracted. |
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Involucres | ovoid to hemispheric, 2–4 × 1.5–6 cm, loosely arachnoid on phyllary margins or glabrate. |
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Receptacles | flat to convex, usually epaleate (often pitted and often bristly-setose or densely hairy). |
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Ray florets | 0 (corollas of peripheral florets in radiant heads often notably enlarged, usually 5-lobed, sometimes zygomorphic and raylike or ± 2-lipped). |
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Peripheral (pistillate) florets | 0 or (in disciform heads) in 1–3+ series; corollas (usually present) usually yellow, sometimes ochroleucous or cyanic. |
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Disc florets | bisexual and fertile (rarely functionally staminate); corollas yellow, cyanic, or white, usually actinomorphic, lobes 5, usually narrowly triangular to ± linear, seldom deltate (sometimes unequal, corollas then ± zygomorphic); anther bases ± tailed, apical appendages usually oblong (filaments sometimes papillate to pilose; connate in Silybum); styles (bisexual, fertile florets) distally enlarged or swollen, usually dilated and/or with rings of hairs at or near point of bifurcation, abaxially smooth or papillate to hairy (at least distally, sometimes ± throughout), “branches” often connate, adaxially continuously stigmatic ± to tips, apices rounded to acute, appendages essentially none. |
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Corollas | white or pale lavender to purple, 20–40 mm, tubes 7–24 mm, throats 4–12 mm (noticeably larger than tubes), lobes 4–10 mm; style tips 3.5–8 mm. |
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Phyllaries | in 5–10 series, imbricate, ovate or lanceolate (outer) to linear or linear-lanceolate (inner), margins (outer) entire or scarious-fringed, abaxial faces without glutinous ridge; outer and mid appressed, spines erect to spreading 0.5–13 mm; apices of mid and inner narrowed and scabro-denticulate or with expanded, erose-dentate tips, spineless or tipped with flattened spines. |
usually persistent [readily falling], in (1–)3–5+ series, usually distinct, usually unequal, usually herbaceous (sometimes fleshy), margins (entire or denticulate to pectinate, sometimes spiny) and apices seldom notably scarious (apices often spinose or ± expanded into distinct, often fimbriate-fringed, pectinate, and/or spiny appendages). |
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Calyculi | 0 (involucres sometimes closely subtended by leaflike peduncle bracts). |
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Heads | 1–many, erect, borne singly or often densely crowded in spiciform, racemiform, or subcapitate arrays, especially in acaulescent or short-caulescent plants, often closely subtended by distalmost leaves. |
mostly homogamous (usually discoid, sometimes disciform or radiant, then peripheral florets usually pistillate or neuter, sometimes bisexual or with staminodes), borne singly or in corymbiform, paniculiform, or racemiform arrays (heads with 1 floret each aggregated into second-order heads in Echinops). |
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Cypselae | light to dark brown, 4–6.5 mm, apical collars usually colored like body; pappi 17–35 mm, white to tan. |
usually monomorphic within heads (often thick-walled, hard, nutlike, receptacular attachments basal or lateral, bases sometimes each with an elaiosome), usually ellipsoid, obovoid, or ovoid, sometimes rounded-prismatic, terete, 4–5-angled, or ± compressed, rarely beaked, bodies usually smooth, sometimes rugose or 10- or 20-nerved (glabrous or puberulent to villous; often with apical umbo and/or crown in addition to pappus); pappi (rarely 0) readily falling or persistent, usually of fine to coarse, barbellate to plumose bristles, sometimes of scales, sometimes both bristles and scales. |
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2n | = 34, 36. |
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Cirsium scariosum |
Asteraceae tribe Cardueae |
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Distribution |
AZ; CA; CO; ID; MT; NM; NV; OR; UT; WA; WY; AB; BC; QC; disjunct to e Que (Mingan Archipelago)
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Mostly Old World; especially Mediterranean [Some species widely introduced] |
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Discussion | Varieties 8 (8 in the flora). Cirsium scariosum is a widely distributed complex of intergrading races distributed from southwestern Canada to northwestern Mexico. These plants range from acaulescent rosettes with a tight cluster of sessile heads to tall, erect, unbranched plants, or moundlike, more or less openly branched herbs. Acaulescent and caulescent plants sometimes occur in the same population. Members of this complex have been variously treated in the past. F. Petrak (1917) recognized ten species plus several subspecies for the taxa I am treating here as C. scariosum (in the broad sense). In floras, the names C. drummondii and C. foliosum have been widely misapplied to these plants (R. J. Moore and C. Frankton 1964). The latter two species, while clearly related to C. scariosum, have a range restricted mostly to Canada. Moore and Frankton (1967) attempted to bring order to the complex and recognized four species for plants that I include here in C. scariosum: C. acaulescens, C. congdonii, C. coloradense, and C. scariosum in the restricted sense. Moore and Frankton substituted the prior name C. tioganum for C. acaulescens. Unfortunately they did not extend their study widely enough and did not include some members of the complex in their investigations. S. L. Welsh (1982) proposed C. scariosum var. thorneae from Utah and lumped the various species recognized by Moore and Frankton within a highly polymorphic var. scariosum. After consulting with A. Cronquist and studying his manuscript treatment of Cirsium for the Intermountain Flora, D. J. Keil and C. E. Turner (1993) also accepted a broadly construed C. scariosum. Cronquist (1994) treated C. scariosum as an extremely variable species that included the four species recognized by Moore and Frankton plus the variety proposed by Welsh. Cronquist chose to not recognize infraspecific taxa. In the present treatment I have examined these plants from a biogeographic perspective with the goal of discerning regional patterns of variation. The large number of specimens available has allowed me to examine distributional patterns in relation to the topography and biogeographic history of the regions where this species occurs. My field studies also have provided me with observations that help to explain some of the anomalous specimens represented in herbaria. Although the variation within and between populations is sometimes amazing, more-or-less differentiated geographic races can be discerned. Because of the extraordinary and overlapping patterns of variation across the range of Cirsium scariosum, the following key to varieties should be regarded as at best an approximation. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Genera 83, species 2500 (17 genera, 116 species in the flora). The circumscription for Cynareae adopted here is the traditional one and includes the three elements (Cynareae in the narrow sense, Carlineae, and Echinopeae) recognized as tribally distinct by M. Dittrich (1977[1978]). Work by K. Bremer (1987) supported the Dittrich scheme. A traditional circumscription of Cynareae was maintained by J. L. Panero and V. A. Funk (2002). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 19, p. 1. | FNA vol. 19, p. 82. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Asteraceae > tribe Cardueae > Cirsium | Asteraceae | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | C. hookerianum var. scariosum | family Asteraceae tribe Cynareae | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | Nuttall: Trans. Amer. Philos. Soc., n. s. 7: 420. (1841) | Cassini | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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