Flora of North America species comparison

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Castilleja thompsonii

Castilleja salsuginosa

Thompson's Indian paintbrush, Thompson's owl clover, Thompson's paintbrush

Monte Neva Indian paintbrush, Monte Neva paintbrush
Habit Herbs, perennial, 0.8–4 dm; from a woody caudex; with a taproot. Herbs, perennial, (0.5–)0.8–1.4(–1.8) dm; from a woody caudex; with a taproot with yellow root hairs.
Stems

few to many, erect or ascending, unbranched or branched, hairs spreading, long, stiff, sometimes soft (especially in higher elevations), eglandular, mixed with shorter stipitate-glandular ones.

several, erect, usually decumbent at base, unbranched, sometimes branched, sometimes with short, leafy axillary shoots, hairs spreading, short, rather stiff, some glandular.
Leaves

green to purple or reddish brown, linear to narrowly oblong or linear-lanceolate, 1.4–7.4 cm, not fleshy, margins plane to ± wavy, involute or flat, 3(–7)-lobed, apex acuminate;

lobes spreading-ascending, linear, short to long moving up leaf axis, apex acute or obtuse.

purplish brown with a grayish cast (due to adhering soil particles and salt crystals), linear to narrowly lanceolate, 1.5–2.5(–3) cm, fleshy, margins plane, sometimes wavy, involute, 0–3(–5)-lobed, apex acute;

lobes spreading, linear to narrowly lanceolate, apex obtuse.
Inflorescences

2.5–14 × 1–4 cm;

bracts greenish to pale yellow or reddish brown throughout, or proximally greenish to dull reddish purple, or ruddy brown, distally greenish to yellow-green or yellow, often aging dull reddish to dull purplish, lanceolate to oblong to ovate, 3–5(–9)-lobed;

lobes spreading to ascending, linear to narrowly lanceolate, long, proximal lobes arising below mid length, apex acute to obtuse.

3–10 × 1.5–5 cm;

bracts proximally purplish, deep burgundy, lavender, dull reddish, or deep purple, distally greenish, white, cream, or pink on margins and apices, oblong, 3(–5)-lobed;

lobes ascending, ± linear, medium length, arising above mid length, central lobe apex rounded to obtuse, expanded distally, lateral ones acute.
Corollas

straight, 18–21 mm;

tube 11–16 mm; subequal to calyx, sometimes beak exserted;

beak adaxially green, 5–7(–8) mm;

abaxial lip white, often proximally reddish, prominent, scarcely expanded, ± cylindric, 2.5–4(–5) mm, 50–70% as long as beak, glabrous or obscurely puberulent;

teeth incurved to erect, white, 2.5 mm.

straight or slightly curved, 18–22(–24) mm;

tube 13–18 mm;

beak, sometimes abaxial lip, exserted;

beak adaxially purplish brown, 4.5–6.5 mm, conspicuously exceeding abaxial lip, margins reddish or colored as bracts, apices white or cream;

abaxial lip reddish purple with green in a distal band or along grooves, gradually inflated, grooved, (2–)3–4(–4.5) mm, 67% as long as beak;

teeth erect to slightly spreading, white to cream, often with purple spot, 1.4–2(–2.5) mm.
Calyces

colored as bracts, 12–25 mm;

abaxial and adaxial clefts 4–8 mm, 20–60% of calyx length, deeper than laterals, lateral (0–)1–3 mm, 7–25% of calyx length;

lobes linear, lanceolate, or triangular, apex acute, sometimes obtuse.

proximally whitish, distally purple to sometimes pink, margins white or cream, 16–20 mm;

abaxial and adaxial clefts 5–8.5 mm, 20–45% of calyx length, all 4 clefts subequal;

lobes linear or narrowly lanceolate, apex obtuse to rounded.
Stigmas

blackish.
2n

= 24, 48.

= 24.

Castilleja thompsonii

Castilleja salsuginosa
Phenology Flowering Apr–Aug(–Sep). Flowering Jun–Jul.
Habitat Dry slopes, ridges, scabland lithosol soils, meadows, sagebrush steppes, valleys, montane to alpine. Damp alkaline clay, hummocks, sparsely vegetated stream banks draining hot springs.
Elevation 200–2100 m. (700–6900 ft.) 1800–2000 m. (5900–6600 ft.)
Distribution
from FNA
OR; WA; BC
[WildflowerSearch map]
[BONAP county map]
from FNA
NV
[BONAP county map]
Discussion

Castilleja thompsonii is a characteristic species of the sagebrush communities on the eastern slope of the Cascade Range in Washington, and in the high deserts of the Columbia Basin. Historically, its range approached but apparently never entered Idaho in the Spokane River valley, but much of its habitat in that area is now converted to agriculture or suburban development or overwhelmed by non-native, invasive plants. Castilleja thompsonii occurs in a few sites in the Okanogan Valley region of southern British Columbia and at one site on the eastern slopes of the Cascade Range in Wasco County, Oregon. A distinctive form from the subalpine and alpine zones of Mt. Adams, in the southern Cascade Range of Washington, was named C. villicaulis. This form may merit varietal status under C. thompsonii. While both names were described in the same paper, C. thompsonii is the name used in all regional floras since their publication, after C. villicaulis was reduced to synonymy by M. Ownbey (1959).

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

Castilleja salsuginosa is endemic to a single site in White Pine County, where it is limited to the harsh alkaline soils of travertine hot springs. This population is threatened by habitat degradation from livestock, as well as by water developments affecting the hydrology of the hot spring system. Castilleja salsuginosa is closely related to C. nana and C. pilosa, but genetic studies of the trio are inconclusive so far. Two populations of very similar but slightly smaller-flowered plants occur around other hot springs in adjacent Eureka County. While they resemble C. salsuginosa superficially, recent morphometric studies of one of these populations indicate that they may be worthy of nomenclatural recognition, separate from C. salsuginosa.

Castilleja salsuginosa is in the Center for Plant Conservation’s National Collection of Endangered Plants.

(Discussion copyrighted by Flora of North America; reprinted with permission.)
Source FNA vol. 17, p. 661. FNA vol. 17, p. 654.
Parent taxa Orobanchaceae > Castilleja Orobanchaceae > Castilleja
Sibling taxa
C. affinis, C. ambigua, C. angustifolia, C. applegatei, C. aquariensis, C. arachnoidea, C. attenuata, C. brevilobata, C. brevistyla, C. campestris, C. cervina, C. chambersii, C. chlorotica, C. christii, C. chromosa, C. chrymactis, C. chrysantha, C. cinerea, C. citrina, C. coccinea, C. collegiorum, C. covilleana, C. crista-galli, C. cryptantha, C. cusickii, C. densiflora, C. dissitiflora, C. disticha, C. elata, C. elegans, C. elmeri, C. exserta, C. flava, C. foliolosa, C. fraterna, C. genevieveana, C. glandulifera, C. gleasoni, C. gracillima, C. grisea, C. haydenii, C. hispida, C. hololeuca, C. hyperborea, C. indivisa, C. integra, C. kaibabensis, C. kerryana, C. kraliana, C. lacera, C. lanata, C. lasiorhyncha, C. lassenensis, C. latifolia, C. lemmonii, C. leschkeana, C. levisecta, C. linariifolia, C. lindheimeri, C. lineariloba, C. lineata, C. litoralis, C. lutescens, C. martini, C. mendocinensis, C. mexicana, C. miniata, C. minor, C. mogollonica, C. mollis, C. montigena, C. nana, C. nelsonii, C. nervata, C. nivea, C. occidentalis, C. oresbia, C. organorum, C. ornata, C. pallescens, C. pallida, C. parviflora, C. parvula, C. patriotica, C. peckiana, C. peirsonii, C. pilosa, C. plagiotoma, C. praeterita, C. pruinosa, C. puberula, C. pulchella, C. purpurascens, C. purpurea, C. raupii, C. revealii, C. rhexiifolia, C. rigida, C. rubicundula, C. rubida, C. rupicola, C. salsuginosa, C. scabrida, C. schizotricha, C. septentrionalis, C. sessiliflora, C. subinclusa, C. suksdorfii, C. tenuiflora, C. tenuis, C. tomentosa, C. uliginosa, C. unalaschcensis, C. victoriae, C. viscidula, C. wightii, C. wootonii, C. xanthotricha
C. affinis, C. ambigua, C. angustifolia, C. applegatei, C. aquariensis, C. arachnoidea, C. attenuata, C. brevilobata, C. brevistyla, C. campestris, C. cervina, C. chambersii, C. chlorotica, C. christii, C. chromosa, C. chrymactis, C. chrysantha, C. cinerea, C. citrina, C. coccinea, C. collegiorum, C. covilleana, C. crista-galli, C. cryptantha, C. cusickii, C. densiflora, C. dissitiflora, C. disticha, C. elata, C. elegans, C. elmeri, C. exserta, C. flava, C. foliolosa, C. fraterna, C. genevieveana, C. glandulifera, C. gleasoni, C. gracillima, C. grisea, C. haydenii, C. hispida, C. hololeuca, C. hyperborea, C. indivisa, C. integra, C. kaibabensis, C. kerryana, C. kraliana, C. lacera, C. lanata, C. lasiorhyncha, C. lassenensis, C. latifolia, C. lemmonii, C. leschkeana, C. levisecta, C. linariifolia, C. lindheimeri, C. lineariloba, C. lineata, C. litoralis, C. lutescens, C. martini, C. mendocinensis, C. mexicana, C. miniata, C. minor, C. mogollonica, C. mollis, C. montigena, C. nana, C. nelsonii, C. nervata, C. nivea, C. occidentalis, C. oresbia, C. organorum, C. ornata, C. pallescens, C. pallida, C. parviflora, C. parvula, C. patriotica, C. peckiana, C. peirsonii, C. pilosa, C. plagiotoma, C. praeterita, C. pruinosa, C. puberula, C. pulchella, C. purpurascens, C. purpurea, C. raupii, C. revealii, C. rhexiifolia, C. rigida, C. rubicundula, C. rubida, C. rupicola, C. scabrida, C. schizotricha, C. septentrionalis, C. sessiliflora, C. subinclusa, C. suksdorfii, C. tenuiflora, C. tenuis, C. thompsonii, C. tomentosa, C. uliginosa, C. unalaschcensis, C. victoriae, C. viscidula, C. wightii, C. wootonii, C. xanthotricha
Synonyms C. villicaulis
Name authority Pennell: Proc. Acad. Nat. Sci. Philadelphia 99: 178. (1947) — (as thompsoni) N. H. Holmgren: Bull. Torrey Bot. Club 100: 83, fig. 1. (1973)
Web links 
Unless otherwise noted, all data comes from the online version of the Flora of North America, who have made most of their content available via a Creative Commons license (CC BY 4.0).



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