Castilleja miniata |
Castilleja exserta |
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common paintbrush, common red paintbrush, giant red Indian paintbrush, great red paintbrush, scarlet Indian paintbrush, scarlet or common or giant red paintbrush, scarlet paintbrush |
castilleja exserta, escobita, exserted Indian paintbrush, owl's clover, purple owl's-clover, purple painted-cup |
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Habit | Herbs, perennial, 1.2–8(–10) dm; from a woody caudex (or slender rooting rhizomes in var. dixonii, var. miniata); with a taproot or with slender, branched roots from a rhizome. | Herbs, annual, 0.1–4.5 dm; with fibrous roots. | ||||||||||||||||||||
Stems | few to many, erect to ascending, rarely proximally decumbent or creeping and rooting at nodes, usually branched, glabrous, glabrate, or hairy, hairs spreading to ± retrorse, short to long, soft to stiff, rarely stipitate-glandular. |
solitary, erect to ascending, unbranched or diffusely branched from near base, hairs spreading, medium length and long, stiff, mixed with short stipitate-glandular ones. |
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Leaves | green to purple, linear to lanceolate, narrowly elliptic, narrowly oblong, or ovate, (1.5–)3–8(–9.5) cm, thin and not fleshy or slightly to moderately thickened and slightly fleshy, margins plane, rarely wavy, flat to involute, whole leaf sometimes recurved downward, 0(–5)-lobed, apex acute to obtuse, sometimes rounded; lobes ascending-spreading, narrowly lanceolate, apex acute. |
green, sometimes purple to brownish, linear or ovate to orbicular in outline, (0.8–)1–5(–7.7) cm, not fleshy, margins plane, involute, (0–)3–9(–11)-lobed, sometimes with secondary lobing, apex acuminate to rounded or acute; lobes spreading, filiform or linear to narrowly spatulate, apex acute to acuminate or rounded. |
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Inflorescences | 3–15(–22) × 1.5–5.5 cm, often bearing a thin, white, powdery exudate, especially on bract surfaces; bracts greenish, scarlet, red, red-orange, or pale orange throughout, sometimes pink, magenta, pink-purple, yellow, greenish yellow, white, or salmon throughout, or proximally greenish, distally colored as above, lanceolate to oblong-ovate, 0–5(–7)-lobed, central lobes sometimes distally apiculate; lobes erect, linear to lanceolate, oblong, or oblanceolate, short or medium length, arising near or above mid length, central lobe apex obtuse, rounded, or truncate, lateral ones rounded to acute or acuminate. |
1.5–20 × 2–4 cm; bracts proximally greenish, dark purple, brownish purple, or white, distally pink, lavender, magenta, light purple, or white on lobe apices, lanceolate to elliptic or narrowly ovate, (3–)5(–9)-lobed, often with 2–4 secondary lobes; lobes ascending to spreading, linear to filiform or narrowly spatulate, medium length to long, arising below or above mid length, apex rounded to acute. |
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Pedicels | 0–5 mm. |
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Corollas | slightly curved, 20–48 mm; tube 12–26 mm; abaxial lip usually not exserted, though often visible in front calyx cleft, beak partially to fully exserted; beak adaxially green to yellow-green or whitish, (9–)14–25 mm; abaxial lip incurved or ascending, deep green or green, sometimes deep purple or yellowish, reduced, not inflated, visible in front cleft, 0.5–3.5 mm, 5–20% as long as beak (to ca. 33% as long as beak in some populations of var. miniata); teeth incurved or erect, green or white, 0.7–1.5 mm. |
straight, 12–33 mm; tube 7–20 mm; beak slightly exserted, hooked near apex, adaxially pink-purple to magenta, rarely white, 5–13 mm, margins colored as bracts, densely villous-hairy; abaxial lip proximally pink, purple, or magenta, rarely yellow or white, with maroon or deep purple distal to that and white to yellow or pink distally, often with purple spots, distal pale color often aging deep pink or deep red, strongly inflated, pouches 3, 3–8 mm wide, 3–4 mm deep, 3–9 mm, 67–80% as long as beak; teeth erect, white, yellow, or purple, often with purple or maroon spots, 0.5–2 mm. |
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Calyces | colored as bracts, 15–38 mm; abaxial and adaxial clefts 4–24 mm, 35–70% of calyx length, deeper than laterals, lateral (1–)3–8(–12) mm, 5–30% of calyx length; lobes linear or narrowly lanceolate to narrowly triangular, apex acute to acuminate or obtuse. |
colored as bracts, 10–26 mm; abaxial clefts 4–12 mm, adaxial 9–18 mm, abaxial ca. 50% of calyx length, adaxial ca. 67% of calyx length, at least adaxial deeper than others, lateral 2.5–9 mm, 15–45% of calyx length; lobes linear (to narrowly oblanceolate), apex rounded to acute. |
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Filaments | with spreading, long, soft hairs. |
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2n | = 24, 48, 72, 96, 120, 144. |
= 24. |
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Castilleja miniata |
Castilleja exserta |
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Distribution |
AK; AZ; CA; CO; ID; MT; NM; NV; OR; UT; WA; WY; AB; BC; MB; ON; SK; YT; nw Mexico
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AZ; CA; NM; nw Mexico
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Discussion | Varieties 4 (4 in the flora). Castilleja miniata is widely recognized as the common scarlet paintbrush. It is highly variable and has five levels of polyploidy. Nonetheless, it remains fairly well defined morphologically across its wide range. Native Americans use it medicinally. A probable hybrid with C. septentrionalis from southern Nevada was named C. ×porterae Cockerell. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Varieties 3 (3 in the flora). In addition to the characters in the key, Castilleja exserta is distinguished from the similar C. densiflora by its conspicuously hairy and apically hooked beak. As a result, the capitate stigma is exserted more or less horizontally from the corolla beak. In contrast, C. densiflora has an unhooked, inconspicuously puberulent beak, from which the stigma emerges more vertically. Castilleja exserta hybridizes with C. attenuata in southern California and with C. lineariloba in central California, and it reportedly crosses occasionally with C. densiflora in southern California. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 17, p. 627. | FNA vol. 17, p. 606. | ||||||||||||||||||||
Parent taxa | Orobanchaceae > Castilleja | Orobanchaceae > Castilleja | ||||||||||||||||||||
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Synonyms | Orthocarpus exsertus | |||||||||||||||||||||
Name authority | Douglas ex Hooker: Fl. Bor.-Amer. 2: 106. (1838) | (A. Heller) T. I. Chuang & Heckard: Syst. Bot. 16: 657. (1991) | ||||||||||||||||||||
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