Castilleja chromosa |
Orobanchaceae |
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desert paintbrush |
broom-rape family |
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Habit | Herbs, sometimes subshrubs, perennial, 1.5–3.5(–4.5) dm; from a woody caudex; with a taproot. | Herbs, rarely subshrubs or shrubs, annual, biennial, or perennial, sometimes fleshy, hemiparasitic or holoparasitic (without chlorophyll) [autotrophic]. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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. |
subterranean or aerial; aerial stems prostrate to decumbent, ascending, or erect [viny]. |
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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. |
deciduous, cauline or basal and cauline, rarely basal only or absent, sometimes scales, opposite, alternate, whorled, or spiral, simple; stipules absent; petiole present or absent; blade usually not fleshy or leathery, rarely fleshy, leathery, or chartaceous, margins entire, toothed, or lobed. |
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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. |
terminal and/or axillary, racemes, panicles, spikes, corymbs, or flowers 1 or 2. |
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Flowers | bisexual, perianth and androecium hypogynous; sepals (0 or)2–5(–8), connate, calyx radially or bilaterally symmetric; petals [4 or]5, connate, corolla bilaterally symmetric, bilabiate or strongly bilabiate, tubular, funnelform, campanulate, salverform, or club-shaped, sometimes cylindric, subrotate, or curved; stamens (2 or)4, adnate to corolla tube, didynamous, subequal, or equal, staminodes 0 or 2; pistil 1, 2[or 3]-carpellate, ovary superior, 1- or 2-locular, placentation axile, sometimes parietal; ovules anatropous or campylotropous-like (Rhinanthus), unitegmic, tenuinucellate; style 1; stigma 1. |
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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. |
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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. |
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Fruits | capsules, dehiscence loculicidal and/or septicidal or indehiscent (Conopholis). |
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Seeds | 1–2500(–5000), brown or black, sometimes tan, white, yellow, amber, or gray, ovoid to ellipsoid, reniform, globular, oblong, or angled; embryo straight, endosperm present. |
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2n | = 24, 48. |
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Castilleja chromosa |
Orobanchaceae |
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Phenology | Flowering (Feb–)Mar–Aug(–Nov). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Dry sagebrush slopes and flats, pinyon-juniper stands, blackbrush, open yellow pine forests. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 500–3200 m. (1600–10500 ft.) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
AZ; CA; CO; ID; NM; NV; OR; UT; WY
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nearly worldwide; especially in warm temperate regions |
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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.) |
Genera ca. 100, species ca. 2000 (27 genera, 292 species in the flora). Orobanchaceae are now defined to include both the holoparasitic members traditionally included in the family (A. Cronquist 1981) and the hemiparasitic genera formerly included in Scrophulariaceae. Although multiple research groups focus on members of the Orobanchaceae, a widely accepted infrafamilial classification of the family in the sense of Angiosperm Phylogeny Group (2016) has not yet appeared. The classification by J. R. McNeal et al. (2013), who found that Orobanchaceae comprise six clades, is followed herein (their named clades are roughly equivalent to tribes). The autotrophic Lindenbergia Lehmann (12 species in the Old World) corresponds to the basal clade sister to the rest of the clades. Species in our region are distributed among the remaining five clades: Cymbarieae D. Don (genus 1), Orobancheae Lamarck & de Candolle (genera 2–6), Rhinantheae Lamarck & de Candolle (genera 7–12), Buchnereae Bentham (genera 13 and 14), and Pedicularideae Duby (genera 15–27). Within the family, genera are arranged alphabetically within tribes, or within Pedicularideae, in subgroups within the tribe. Parasitic plants attach to their hosts via haustoria (L. J. Irving and D. D. Cameron 2009). Haustoria are produced by both hemiparasitic and holoparasitic Orobanchaceae (E. Fischer 2004). In hemiparasitic taxa, haustoria usually tap their host’s xylem, mostly taking up water, mineral nutrients, and nitrogen from their host, and sometimes also carbon. Holoparasitic taxa derive all of their growth requirements predominantly from the host’s phloem (Irving and Cameron). Parasitism has evolved once in the family (N. D. Young et al. 1999; J. R. McNeal et al. 2013); holoparasitism has arisen independently three times from the hemiparasitic condition (J. R. Bennett and S. Mathews 2006; McNeal et al.). Some Orobanchaceae are serious pests, primarily on legume and grain crops in warmer and drier areas, especially in sub-Saharan Africa. Striga is a particularly serious pest that parasitizes mostly monocots; S. gesnerioides attacks eudicots (K. I. Mohamed et al. 2006). Orobanche parasitizes eudicot crops primarily in temperate parts of the world (E. S. Teryokhin 1997). All Striga species and non-native species of Orobanche in the flora area are listed on the Federal Noxious Weed List (http://www.aphis.usda.gov/plant_health/plant_pest_info/weeds/downloads/weedlist.pdf) in the United States. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Source | FNA vol. 17, p. 595. | FNA vol. 17, p. 456. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Orobanchaceae > Castilleja | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Synonyms | C. ewanii, C. martini subsp. ewanii, C. martini var. ewanii | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | A. Nelson: Bull. Torrey Bot. Club 26: 245. (1899) — (as Castilleia) | Ventenat | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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