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Hooker's thistle, white thistle

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

Habit Biennials or monocarpic (sometimes polycarpic?) perennials, 20–150 cm; taprooted. Biennials or monocarpic perennials, 20–100 cm; deeply taprooted.
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, thinly to densely gray-tomentose with fine, non-septate trichomes;

branches 0–many, ascending.

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 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.

Peduncles

0–8+ cm.

0–25 cm.

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.

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

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.

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.

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 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.

Heads

1–many, borne singly or crowded in spiciform, racemiform, subcapitate, or sometimes more openly branched corymbiform arrays.

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

Cypselae

dark brown, 5–6.5 mm, apical collars not differentiated;

pappi 18–22 mm.

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

pappi 12–25 mm.

2n

= 34.

= 32, 34, 36.

Cirsium hookerianum

Cirsium inamoenum

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
from FNA
ID; MT; WA; WY; AB; BC
[WildflowerSearch map]
[BONAP county map]
from FNA
CA; ID; NV; OR; UT; WA; WY
[WildflowerSearch map]
[BONAP county map]
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 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.)

Key
1. Corollas white or pale lavender
var. inamoenum
1. Corollas lavender to rich pink-purple
var. davisii
Source FNA vol. 19, p. 148. FNA vol. 19, p. 134.
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. 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
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
Subordinate taxa
C. inamoenum var. davisii, C. inamoenum var. inamoenum
Synonyms C. kelseyi Carduus inamoenus
Name authority Nuttall: Trans. Amer. Philos. Soc., n. s. 7: 418. (1841) (Greene) D. J. Keil: Sida 21: 214. (2004)
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