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Christ's Indian paintbrush, John Christ's paintbrush

Habit Herbs, perennial, 1.4–3 dm; from a woody caudex; with a taproot.
Stems

several, erect to ascending, unbranched, sometimes branched, glabrous or hairs spreading, short and long, ± stiff, sometimes stipitate-glandular especially distally.

Leaves

green, narrowly to broadly lanceolate, (1–)2–5(–6) cm, not fleshy, margins plane, flat or involute, (0–)3(–5)-lobed, apex acute to rounded;

lobes erect or ascending, linear, lanceolate, or triangular, sometimes very small, apex acute to rounded.

Inflorescences

3–6 × 2–4 cm;

bracts proximally greenish, distally pale orange or pale yellow, sometimes red-orange, lanceolate or narrowly elliptic to ovate, sometimes obovate, 3–5-lobed;

lobes ascending, linear, medium length to long, arising at or below mid length, apex acute to obtuse.

Corollas

straight, 20–30 mm;

tube 12–19 mm;

beak exserted, adaxially green, 7–12 mm;

abaxial lip green, reduced, included or visible through cleft, 1.5–2 mm, 10–20% as long as beak;

teeth incurved, deep green, 1.5 mm.

Calyces

colored as bracts, 17–22(–24) mm;

abaxial clefts 9–12(–13) mm, adaxial 7–11 mm, clefts 50% of calyx length, deeper than laterals, lateral 2–6.5(–8.5) mm, 20–50% of calyx length;

lobes lanceolate to narrowly lanceolate, apex acute to obtuse.

Castilleja christii

Phenology Flowering Jun–Jul.
Habitat Gentle slopes, mostly northern aspect, in herbaceous or grassy subalpine to alpine meadows, sagebrush openings and swales, snowbank communities, over quartzite.
Elevation 2100–2900 m. (6900–9500 ft.)
Distribution
from FNA
ID
[WildflowerSearch map]
[BONAP county map]
Discussion

Castilleja christii is endemic to subalpine meadows near the summit of Mt. Harrison in the Albion Mountains, Cassia County. Morphologically, it most closely resembles the widespread C. hispida var. acuta, but a recent molecular study (D. L. Clay et al. 2012) presents clear evidence for a homoploid hybrid origin for the species, incorporating portions of the genomes of C. linariifolia and C. miniata. This is the first documented case of homoploid origin in Castilleja.

Castilleja christii 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. 595.
Parent taxa 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. 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. thompsonii, C. tomentosa, C. uliginosa, C. unalaschcensis, C. victoriae, C. viscidula, C. wightii, C. wootonii, C. xanthotricha
Name authority N. H. Holmgren: Bull. Torrey Bot. Club 100: 91, fig. 5. (1973)
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