Cirsium altissimum |
Cirsium grahamii |
|
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roadside thistle, tall thistle |
Graham's thistle |
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Habit | Biennials or short-lived monocarpic perennials, (50–)100–300(–400) cm; taproots and often a cluster of coarse fibrous roots, roots without tuberlike enlargements. | Biennials, 50–100 cm; taproots slender and fascicles of thick fibrous roots. |
Stems | single, erect, villous with septate trichomes, sometimes ± glabrate, sometimes distally thinly tomentose; branches few–many, ascending. |
1, erect, thinly arachnoid and/or puberulent to short-pilose, sometimes ± glabrate; branches 0–4, ascending. |
Leaves | blades oblanceolate to elliptic or ovate, 10–40 × 1–13 cm, margins flat, finely spiny-toothed and otherwise undivided to coarsely toothed or shallowly pinnatifid, lobes broadly triangular, main spines 1–5 mm, abaxial faces white-tomentose, adaxial faces green, glabrate to villous with septate trichomes; basal usually absent at flowering, winged-petiolate, bases tapered; principal cauline well distributed, gradually reduced, bases narrowed, sometimes weakly clasping; distal cauline well developed. |
blades oblanceolate to oblong-elliptic, 20–30 × 3–8 cm, spinulose and otherwise entire or coarsely dentate to deeply pinnatifid, lobes entire or coarsely few toothed or lobed, main spines slender, 3–6 mm, abaxial ± persistently gray-tomentose, sometimes pilose along veins, adaxial faces thinly arachnoid and ± glabrate; basal often present at flowering, sessile or narrowly winged-petiolate; principal cauline gradually winged-petiolate or sessile, reduced distally, bases sometimes clasping or short-decurrent; distal cauline ascending, becoming bractlike, narrow, lobed or not. |
Peduncles | 0–5 cm (leafy-bracted). |
10–30 cm. |
Involucres | ovoid to broadly cylindric or campanulate, (2–)2.5–3.5(–4) × (1.5–)2–3(–4) cm, thinly arachnoid. |
hemispheric, 2–3 × 2–4 cm, thinly arachnoid or glabrous. |
Style | tips 4–6 mm. |
|
Corollas | pink to purple (white), 20–35 mm, tubes 10–16 mm, throats 5–12 mm, lobes 5–9 mm. |
deep purple, 22–30 mm, tubes 13–18 mm, throats 4–5 mm, lobes 5–8 mm; style tips 4–4.5 mm. |
Phyllaries | in 10–20 series, strongly imbricate, greenish with subapical darker central zone, ovate (outer) to lanceolate (inner), abaxial faces with a narrow glutinous ridge (milky when fresh, dark when dry), outer and middle entire, bodies appressed, spines slender, abruptly spreading, 3–4 mm; apices of inner phyllaries spreading, narrow, flattened, entire, spines spreading, slender, 3–4 mm; apices of inner phyllaries spreading, narrow, flattened, ± dilated, ± erose or finely serrulate. |
in ca. 8 series, imbricate, proximally brownish, distally dark purplish, lanceolate to linear, margins of outer hispidulous-ciliolate, spiny fringed, pinnately spiny or with scarious appendages, abaxial faces with prominent, glutinous ridge; outer and middle appressed or only apices spreading, bodies minutely spinulose-denticulate, spines erect to ascending, 1.5–2.5 mm; apices of inner phyllaries often flexuous, flat, scabridulous. |
Heads | 1–many, in corymbiform or paniculiform arrays, (± elevated above principal cauline leaves), not subtended by ring of spiny bracts. |
1–5. |
Cypselae | tan to dark brown, 4–5.5 mm, apical collars stramineous, 0.5–1 mm; pappi 12–24 mm. |
tan with dark speckles to dark purplish brown, 4–5.5 mm, apical collars not differently colored; pappi 13–18 mm. |
2n | = 18. |
= 32 (Mexico). |
Cirsium altissimum |
Cirsium grahamii |
|
Phenology | Flowering summer–fall (Jun–Oct). | Flowering Jul–Sep. |
Habitat | Prairies, woodlands, disturbed sites, often in damp soil | Oak woodlands, coniferous forests, meadows, often in damp soil |
Elevation | 50–700 m (200–2300 ft) | 1400–2600 m (4600–8500 ft) |
Distribution |
AL; AR; DC; DE; FL; GA; IA; IL; IN; KS; KY; LA; MA; MD; MI; MN; MO; MS; NC; ND; NE; NY; OH; OK; PA; SC; SD; TN; TX; WI; WV
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AZ; NM; Mexico (Chihuahua, Durango, Sonora)
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Discussion | Plants of Cirsium altissimum ranging from southern Minnesota to Texas often have more deeply divided leaves than do populations in other portions of the species’ range. Some botanists (e.g., R. J. Moore and C. Frankton 1969; D. S. Correll and M. C. Johnston 1970) have treated those plants as C. iowense. Others (e.g., R. E. Brooks 1986; H. A. Gleason and A. Cronquist 1991; G. B. Ownbey and T. Morley 1991) have treated them as C. altissimum. Still others considered them to be derivatives of hybridization between C. altissimum and C. discolor (J. T. Kartesz and C. A. Meacham 1999) and treated them as C. ×iowense. Indeed the existence of these plants blurs the distinction between C. altissimum and C. discolor, and herbarium specimens are often difficult to assign. Natural hybrids between Cirsium altissimum and C. discolor are well documented (R. A. Davidson 1963; G. B. Ownbey and Hsi Y.-T. 1963; Ownbey 1964; S. Dabydeen 1997). Ownbey and Dabydeen both reported that apparent F1 hybrids between the two species have low seed set in comparison with the parental taxa. W. L. Bloom (1977) reported that the chromosomes of the two species differ by several rearareaments. Dabydeen reported a count of 2n = 19 with multiple meiotic irregularities for an apparent F1 hybrid. However, the presence of numerous individuals and populations seemingly intermediate between C. altissimum and C. discolor indicates that although F1 hybrids have low fertility, long-term processes may have stabilized hybrid derivatives of higher fertility. Ownbey and Hsi reported mitotic counts of 2n = 18 and 20 from a population that they treated as C. altissimum. In their discussion they noted that their plants represented “the segregate called C. iowense” and had been collected a short distance from that taxon’s type locality. R. J. Moore and C. Frankton (1969) reported a chromosome number of 2n = 18 for a plant from Texas that they considered to be C. iowense. Further investigation of morphologic variation, chromosome number, meiotic behavior, and fertility is needed of populations named as C. iowense to determine how those plants should be treated. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Cirsium grahamii occurs in the mountains of southeastern Arizona and southwestern New Mexico. It forms hybrid swarms with C. parryi and C. scariosum var. coloradense in the White Mountains of Arizona. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 19, p. 111. | FNA vol. 19, p. 124. |
Parent taxa | Asteraceae > tribe Cardueae > Cirsium | Asteraceae > tribe Cardueae > Cirsium |
Sibling taxa | ||
Synonyms | Carduus altissimus, C. altissimum var. biltmoreanum, C. iowense | |
Name authority | (Linnaeus) Sprengel: Syst. Veg. 3: 373. (1826) | A. Gray: Smithsonian Contr. Knowl. 5(6): 102. (1853) |
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