Castilleja viscidula |
Orobanchaceae |
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sticky Indian paintbrush, sticky paintbrush |
broom-rape family |
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Habit | Herbs, perennial, 0.5–3(–4) 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, ascending to erect, decumbent at base, unbranched, sometimes branched, hairs spreading, long, soft, mixed with shorter stipitate-glandular ones. |
subterranean or aerial; aerial stems prostrate to decumbent, ascending, or erect [viny]. |
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Leaves | green to brown, linear, linear-lanceolate, lanceolate, or oblong (narrowly ovate nearing inflorescence), 1–4(–5) cm, not fleshy, margins wavy, flat or involute, (0–)2(–5)-lobed, apex acute; lobes ascending-spreading, oblong to narrowly lanceolate, apex acute or obtuse. |
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 | 2–14 × 1–3.5 cm; bracts proximally greenish to greenish brown, distally pale yellow, cream, or yellow-green, sometimes yellow-orange or red (sometimes gradually differentiated from proximal coloration), lanceolate, broadly lanceolate, or oblong, 3(–5)-lobed, proximal wavy-margined; lobes ascending, linear to narrowly lanceolate, long, arising near or above mid length, sometimes wavy-margined, apex acute to rounded. |
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, 16–22(–25) mm; tube 10–15 mm; beak exserted, straight to sometimes curved, adaxially green to yellow, 5–8(–9) mm; abaxial lip green or yellow, sometimes deep purple, reduced, inconspicuous, often visible in abaxial cleft, 1–2 mm, 20% as long as beak; teeth erect, green to white, sometimes yellow or pink, 0.5–1 mm. |
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Calyces | colored as bracts or proximally paler, (10–)14–18 mm; abaxial and adaxial clefts (4–)5–9 mm, 30–40% of calyx length, deeper than laterals, lateral (1–)2–6 mm, ca. 25% of calyx length; lobes narrowly ovate to lanceolate, linear, or narrowly lanceolate, apex acute to obtuse. |
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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, 72. |
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Castilleja viscidula |
Orobanchaceae |
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Phenology | Flowering Jun–Aug. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Dry to mesic sagebrush steppes, rocky slopes, ledges, open woodlands, montane to subalpine. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 2000–3200 m. (6600–10500 ft.) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
ID; NV; OR
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nearly worldwide; especially in warm temperate regions |
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Discussion | Castilleja viscidula is a member of the complex including C. applegatei and C. martini, centered in California. Castilleja viscidula favors isolated mountain ranges, from the Wallowa and, possibly, the Blue mountains of northeastern Oregon, eastward into southwestern Idaho, and southward into central Nevada. Most populations are greenish yellow, but in one portion of the Wallowa Mountains, reddish bracted plants are common. Many yellowish bracted populations in the same mountain range surround this reddish population. Intermediate color forms are rarely encountered. Most ranges where C. viscidula occurs have generated slightly differing local races, demonstrating some reproductive isolation and divergence. In addition, hybrid swarms between this species and C. nana are known from several mountain ranges in central and northern Nevada, and an apparent hybrid with C. flava var. flava is known from the Independence Mountains of northern Nevada. (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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Key |
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Source | FNA vol. 17, p. 664. | FNA vol. 17, p. 456. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Orobanchaceae > Castilleja | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | A. Gray: in A. Gray et al., Syn. Fl. N. Amer. 2(1): 297. (1878) — (as Castilleia) | Ventenat | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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