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Davis' thistle, Greene's thistle, intermountain thistle, Jackson hole thistle

chardon de Flodman, Flodman's thistle, prairie thistle

Habit Biennials or monocarpic perennials, 20–100 cm; deeply taprooted. Perennials 30–140 cm; horizontal runner roots that produce root sprouts.
Stems

1–several, erect, thinly to densely gray-tomentose with fine, non-septate trichomes;

branches 0–many, ascending.

1–several, erect, gray- or white-tomentose;

branches 0–few, ascending.

Leaves

blades oblanceolate or elliptic, 10–35 × 1–7 cm, unlobed and spinulose to dentate or deeply pinnatifid, usually 5–8 pairs of lobes, well separated, linear to lance-triangular, spinulose to few toothed or lobed, main spines 2–7 mm, abaxial faces densely gray-tomentose or sometimes ± glabrate, adaxial gray to ± green, thinly tomentose or ± glabrate;

basal sometimes present at flowering, narrowly winged-petiolate;

principal cauline well distributed, gradually reduced, sometimes spinier than basal;

proximal winged-petiolate, mid sessile, bases spiny-winged, decurrent 1–3 cm;

distal becoming bractlike, often unlobed or less deeply divided than proximal.

blades oblong-oblanceolate to narrowly elliptic, 4–40 × 1–10 cm, bases usually not decurrent, finely spiny-toothed and undivided to coarsely toothed or deeply pinnatifid, lobes broadly triangular to linear-lanceolate, often revolute-margined, main spines 1–7 mm, abaxial faces white-tomentose, adaxial faces green, thinly tomentose, ± glabrate;

basal usually absent or withered at flowering, winged petiolate;

principal cauline proximally winged-petiolate, distally sessile, well distributed, gradually reduced, bases usually not decurrent;

distal cauline well developed.

Peduncles

0–25 cm.

0–5 cm (elevated above distal leaves).

Involucres

ovoid or hemispheric to campanulate, 2–3 × 1.5–5 cm, glabrous or loosely floccose to densely arachnoid.

ovoid to broadly campanulate, 2–3.5 × 2.5–3.5 cm, thinly arachnoid.

Corollas

dull white or faintly lavender-tinged to bright pink-purple, 19–31 mm, tubes 7–13 mm, throats 6.5–9.5 mm, lobes 4–8 mm;

style tips 3.5–7 mm.

purple (white), 23–36 mm, tubes 12–15 mm, throats 6–8.5 mm, lobes 5–9 mm;

style tips 4–7 mm.

Phyllaries

in 6–10 series, strongly imbricate or sometimes subequal, greenish to brown, ovate to linear-lanceolate (outer) to linear (inner), entire, abaxial faces with narrow or scarcely developed glutinous ridge;

outer and mid appressed or apices ascending to spreading, linear, bodies entire, spines ascending to abruptly spreading, usually fine, 2–6 mm;

apices of inner narrow, spine-tipped or spineless.

in 7–12 series, strongly imbricate, greenish with subapical darker central zone, ovate or lanceolate (outer) to linear (inner), abaxial faces with prominent glutinous ridge;

outer and middle entire, bodies appressed, entire, acute, spines abruptly spreading, slender, 2–4 mm;

apices of inner spreading, flexuous, narrow, flattened, finely serrulate, ± scabrous.

Heads

1–many, in open corymbiform arrays or crowded near stem tips.

erect, borne singly and terminal on main stem and branches, or few in corymbiform arrays from distal axils (not subtended by ring of spiny-margined bracts).

Cypselae

brown, 5–8 mm, apical collars not differentiated;

pappi 12–25 mm.

light brown, 3–5 mm, apical collars stramineous, 0.5–1 mm;

pappi (white or tawny) 20–30 mm.

2n

= 32, 34, 36.

= 22, 24.

Cirsium inamoenum

Cirsium flodmanii

Phenology Flowering summer (Jun–Sep).
Habitat Tallgrass, mixedgrass, shortgrass prairies, meadows, pastures, often in damp soil
Elevation 100–2400 m (300–7900 ft)
Distribution
from FNA
CA; ID; NV; OR; UT; WA; WY
[WildflowerSearch map]
[BONAP county map]
from FNA
CO; IA; IL; KS; MI; MN; MT; ND; NE; SD; WI; WY; AB; MB; ON; QC; SK
[WildflowerSearch map]
[BONAP county map]
Discussion

Varieties 2 (2 in the flora).

Cirsium inamoenum is a variable complex across the northern Great Basin and adjacent mountains. A. Cronquist (1994) treated this complex as a single species under the name C. subniveum without infraspecific taxa and including taxa that formerly had been assigned to C. utahense (e.g., J. T. Howell 1960b). Some populations consist of small-headed, white-flowered plants with strong involucres and short, appressed phyllaries. Others have larger heads, white or lavender to pink-purple corollas, and phyllaries with longer, ascending to spreading tips. My treatment of this complex as C. inamoenum is similarly inclusive as was Cronquist’s treatment of C. subniveum, except that I believe C. humboldtense, which Cronquist included, is probably a derivative of hybridization between C. subniveum and C. eatonii var. peckii. I have observed such hybrids on the slopes of Steens Mountain in Harney County, Oregon, and the type of C. humboldtense closely resembles some of the introgressants. I have examined several other specimens that are likely the products of hybridization of C. inamoenum with other varieties of C. eatonii.

I have chosen to recognize racial differentiation within Cirsium inamoenum at the rank of variety. The main difference between Cirsium inamoenum var. inamoenum and var. davisii is corolla color. Unfortunately this feature is sometimes difficult to determine on herbarium specimens, and many collectors fail to include corolla color on specimen labels. Some geographic overlap occurs between var. davisii, which has a distribution centered in northeastern Utah, southeastern Idaho, and adjacent southwestern Wyoming, and the more widespread var. inamoenum.

Plants of northeastern Oregon, southeastern Washington, and adjacent western Idaho often have large heads and densely tomentose foliage. These were named Cirsium wallowense by Peck. Similar plants occur sporadically in other portions of the range of Cirsium inamoenum var. inamoenum and I chose not to recognize these northwestern populations as a third variety. Additional study might clarify the relationships of these plants.

Some specimens of Cirsium inamoenum in central Nevada and Utah approach C. neomexicanum. It seems likely that these species have interacted in the past.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Cirsium flodmanii ranges from Saskatchewan and Alberta south through the northern Great Plains and intermountain valleys of Montana and Wyoming to northeastern Colorado and east through the prairies to Minnesota and Iowa, and in widely scattered locations eastward to northern Illinois, southern Wisconsin, southern Ontario, and southern Quebec. It is known to hybridize with C. muticum and C. undulatum. Hybrids between C. flodmanii and C. undulatum are highly sterile with numerous meiotic irregularities (S. Dabydeen 1987).

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Corollas white or pale lavender
var. inamoenum
1. Corollas lavender to rich pink-purple
var. davisii
Source FNA vol. 19, p. 134. FNA vol. 19, p. 120.
Parent taxa Asteraceae > tribe Cardueae > Cirsium Asteraceae > tribe Cardueae > Cirsium
Sibling taxa
C. altissimum, C. andersonii, C. andrewsii, C. arizonicum, C. arvense, C. barnebyi, C. brevifolium, C. brevistylum, C. canescens, C. carolinianum, C. ciliolatum, C. clavatum, C. crassicaule, C. cymosum, C. discolor, C. douglasii, C. drummondii, C. eatonii, C. edule, C. engelmannii, C. flodmanii, C. foliosum, C. fontinale, C. grahamii, C. helenioides, C. hookerianum, C. horridulum, C. hydrophilum, C. joannae, C. kamtschaticum, C. lecontei, C. longistylum, C. mohavense, C. muticum, C. neomexicanum, C. nuttallii, C. occidentale, C. ochrocentrum, C. ownbeyi, C. palustre, C. parryi, C. perplexans, C. pitcheri, C. praeteriens, C. pulcherrimum, C. pumilum, C. quercetorum, C. remotifolium, C. repandum, C. rhothophilum, C. rydbergii, C. scariosum, C. texanum, C. tracyi, C. turneri, C. undulatum, C. vinaceum, C. virginianum, C. vulgare, C. wheeleri, C. wrightii
C. altissimum, C. andersonii, C. andrewsii, C. arizonicum, C. arvense, C. barnebyi, C. brevifolium, C. brevistylum, C. canescens, C. carolinianum, C. ciliolatum, C. clavatum, C. crassicaule, C. cymosum, C. discolor, C. douglasii, C. drummondii, C. eatonii, C. edule, C. engelmannii, C. foliosum, C. fontinale, C. grahamii, C. helenioides, C. hookerianum, C. horridulum, C. hydrophilum, C. inamoenum, C. joannae, C. kamtschaticum, C. lecontei, C. longistylum, C. mohavense, C. muticum, C. neomexicanum, C. nuttallii, C. occidentale, C. ochrocentrum, C. ownbeyi, C. palustre, C. parryi, C. perplexans, C. pitcheri, C. praeteriens, C. pulcherrimum, C. pumilum, C. quercetorum, C. remotifolium, C. repandum, C. rhothophilum, C. rydbergii, C. scariosum, C. texanum, C. tracyi, C. turneri, C. undulatum, C. vinaceum, C. virginianum, C. vulgare, C. wheeleri, C. wrightii
Subordinate taxa
C. inamoenum var. davisii, C. inamoenum var. inamoenum
Synonyms Carduus inamoenus Carduus flodmanii, C. oblanceolatum
Name authority (Greene) D. J. Keil: Sida 21: 214. (2004) (Rydberg) Arthur: Torreya 12: 34. (1912)
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