Castilleja chromosa |
Castilleja lacera |
|
---|---|---|
desert paintbrush |
cut-leaf owl's clover, cut-leaf paintbrush, cutleaf Indian paintbrush, foothill owl's clover |
|
Habit | Herbs, sometimes subshrubs, perennial, 1.5–3.5(–4.5) dm; from a woody caudex; with a taproot. | Herbs, annual, 0.5–4 dm; with fibrous roots. |
Stems | several to many, ascending to erect, often grayish, unbranched, rarely branched, sometimes with short, leafy axillary branches, hairs spreading-erect, long, stiff, eglandular, sometimes also with shorter, stipitate-glandular ones. |
solitary, erect, unbranched or branched, hairs spreading, long, soft, scattered among more numerous, medium length, stipitate-glandular ones. |
Leaves | gray-green, linear, lanceolate, or oblanceolate, sometimes broadly lanceolate, (1.5–)2.5–6(–7) cm, not fleshy, margins plane, involute, (0–)3–5(–7)-lobed, sometimes with secondary lobes, apex acuminate to obtuse; lobes spreading, linear, apex acuminate. |
green or purplish, linear to narrowly lanceolate, 1–5 cm, not fleshy, margins plane, flat, 0–5(–7)-lobed, apex acuminate; lobes spreading to ascending, linear, apex acuminate to acute. |
Inflorescences | 2.5–15 (much longer in fruit) × 1.5–5.5 cm; bracts proximally greenish to dull purplish, distally bright red to scarlet or orange-red, rarely yellowish to dull orange or pink, narrowly to broadly linear or lanceolate, narrowly ovate, or oblong-lanceolate, (0–)3–7-lobed, rarely with secondary lobes; lobes spreading, linear to oblong, sometimes oblanceolate, often expanded near tip, long, proximal lobes arising below mid length, apex rounded or obtuse to sometimes acute. |
(1.5–)3–14 × 2–3 cm; bracts green throughout, sometimes proximally green, distally white on apices, lanceolate to ovate, 3–7-lobed; lobes spreading to ascending, linear to narrowly lanceolate, long, arising below mid length, apex obtuse to acute. |
Corollas | straight or ± curved, 18–35(–40) mm; tube 8–15 mm; beak short- or long-exserted, adaxially green to yellow-green, (9–)10–18 mm; abaxial lip deep green, reduced, thickened, included to exserted, 2–3 mm, ca. 20% as long as beak; teeth incurved, deep green, 0.5–1 mm. |
straight, 10–22 mm; tube 8–15 mm; abaxial lip and beak exserted; beak adaxially yellow to greenish, 3–6 mm, densely puberulent; abaxial lip yellow with purple dots at base, inflated, pouches 3, central pouch slightly 2-lobed, pouches 4–8 mm wide, 3–6 mm deep, side pouches curving up a little at tip, 2–5 mm, 75–95% as long as beak; teeth erect, white or yellow, 0.5–2 mm. |
Calyces | colored as bracts, sometimes with broad yellow band below colored lobe apices, (17–)20–27 mm; abaxial clefts 4–10 mm, adaxial 6–12 mm, abaxial ca. 30% of calyx length, adaxial ca. 40% of calyx length, deeper than laterals, lateral 1–4 mm, ca. 15% of calyx length; lobes oblong or ovate to narrowly triangular or lanceolate, apex obtuse to rounded. |
light green, lobes green, 7–13 mm; abaxial and adaxial clefts 3.5–8 mm, 50–67% of calyx length, lateral 2.5–5 mm, ca. 40% of calyx length; lobes narrowly to broadly lanceolate, apex acute to acuminate. |
Stigmas | equal to or slightly exserted from beak. |
|
2n | = 24, 48. |
= 22, 24. |
Castilleja chromosa |
Castilleja lacera |
|
Phenology | Flowering (Feb–)Mar–Aug(–Nov). | Flowering (Mar–)Apr–Jul(–Aug). |
Habitat | Dry sagebrush slopes and flats, pinyon-juniper stands, blackbrush, open yellow pine forests. | Grasslands, meadows, moist flats, vernal pool margins, moist forest openings, serpentine slopes and ledges, roadsides. |
Elevation | 500–3200 m. (1600–10500 ft.) | 0–2700 m. (0–8900 ft.) |
Distribution |
AZ; CA; CO; ID; NM; NV; OR; UT; WY
|
CA; OR
|
Discussion | Castilleja chromosa is sometimes confused with 3b. C. angustifolia var. dubia (see discussion there). Castilleja chromosa retains its distinctive morphology across its wide range and is a characteristic species of much of the southwestern United States. Where it overlaps with C. angustifolia, the two are distinguished by inflorescence color and width and by the lengths of the calyx, corolla, and corolla beak. In the broad region of their sympatry, there is little evidence of intergradation, except in a few sites in Elko County, Nevada, and in southern Wyoming. Throughout southern Idaho and northeastern Nevada the range of the two overlap with little or no intergradation. At high elevations in Montrose County, Colorado, C. chromosa has narrower leaves and a longer and silkier pubescence, especially in the inflorescence. Apparent hybrids between C. chromosa and C. flava var. rustica are known from Custer County, Idaho, and hybrids with C. linariifolia are known from Montrose County, Colorado. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Castilleja lacera is found in a wide range of elevations in the central and northern Sierra Nevada region and in the Siskiyou Mountains region of northwestern California and southwestern Oregon. Reports from the Coast Ranges north of the San Francisco Bay region and south of the Siskiyou region in western California are referable to other yellow-flowered annuals, including C. ambigua, C. rubicundula var. lithospermoides, Triphysaria eriantha subsp. eriantha, and T. versicolor subsp. faucibarbata. Although most similar to C. rubicundula, C. lacera is somewhat smaller in stature and flower size. It is also easily confused with yellow-flowered populations of C. tenuis, which has smaller flowers and an included stigma. Two chromosome numbers are known for this species, the more northern populations being diploid, and those to the south having an apparently aneuploid count of 2n = 22, which is unique in the genus. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 17, p. 595. | FNA vol. 17, p. 617. |
Parent taxa | Orobanchaceae > Castilleja | Orobanchaceae > Castilleja |
Sibling taxa | ||
Synonyms | C. ewanii, C. martini subsp. ewanii, C. martini var. ewanii | Orthocarpus lacerus |
Name authority | A. Nelson: Bull. Torrey Bot. Club 26: 245. (1899) — (as Castilleia) | (Bentham) T. I. Chuang & Heckard: Syst. Bot. 16: 657. (1991) |
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