Orobanche uniflora |
Orobanchaceae |
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cancer root, ghost pipe, naked broomrape, one-flower broom-rape, one-flower cancer-root, orobanche uniflore, small cancer-root |
broom-rape family |
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Habit | Plants simple or few-branched basally, sometimes forked medially, 3.5–18(–25) cm (including pedicels), stem portion 1–5(–7) cm, slender, base not enlarged. | Herbs, rarely subshrubs or shrubs, annual, biennial, or perennial, sometimes fleshy, hemiparasitic or holoparasitic (without chlorophyll) [autotrophic]. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Roots | inconspicuous, slender or stout, unbranched or few-branched. |
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Stems | subterranean or aerial; aerial stems prostrate to decumbent, ascending, or erect [viny]. |
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Leaves | relatively few, loosely imbricate or more remote, loosely ascending to spreading; blade oblong-lanceolate to awl-shaped, 2–10 mm, margins entire, often inrolled, apex acuminate, surfaces glabrous. |
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 | of solitary flowers or fascicles of 2(–4) at stem or branch tips, white to cream, sometimes purple tinged, simple, glabrous; bracts loosely ascending and erect, oblanceolate to broadly ovate, obovate, rhombic, or awl-shaped, 5–12 mm, apex acute to acuminate, glabrous, rarely glandular-pubescent distally. |
terminal and/or axillary, racemes, panicles, spikes, corymbs, or flowers 1 or 2. |
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Pedicels | (8–)20–110(–170) mm, much longer than plant axis; bracteoles 0. |
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Flowers | calyx white to straw colored or light yellow, or pale to dark, dull purple, sometimes brownish, ± radially symmetric, 4–12(–15) mm, divided into 5 subequal lobes, lobes slightly shorter than to 2 times as long as tube, ± triangular or subulate-triangular, sparsely to moderately glandular-pubescent; corolla (11–)15–30(–35) mm, tube white to purple, blue, or yellow, sometimes lighter proximally or with light or darker purple or blue veins, slightly to moderately constricted above ovary, ± bent forward, glandular-pubescent; palatal folds ± prominent, bright yellow, glandular- and/or eglandular-pubescent, sometimes glabrescent; lips white, yellow, purple, or blue, sometimes with light or darker purple or blue veins, abaxial lip slightly to moderately spreading, sometimes ± recurved distally, (1–)2–6(–9) mm, lobes oblong-obovate to nearly round, apex rounded to bluntly pointed or shallowly emarginate (sometimes with 2 notches), adaxial lip slightly to moderately spreading, sometimes recurved, 2–6(–9) mm, lobes broadly oblong-ovate to oblong-semiorbiculate, apex rounded, rarely bluntly pointed or shallowly emarginate; filaments glabrous, anthers included, glabrous or villous-tomentose. |
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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Fruits | capsules, dehiscence loculicidal and/or septicidal or indehiscent (Conopholis). |
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Capsules | ovoid to oblong-ovoid, 4–8(–11) mm. |
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Seeds | 0.1–0.4 mm. |
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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Orobanche uniflora |
Orobanchaceae |
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Distribution |
AK; AR; AZ; CA; CO; CT; DC; DE; FL; IA; ID; IL; IN; KS; KY; MA; MD; ME; MI; MN; MO; MS; MT; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OK; OR; PA; RI; SC; TN; TX; UT; VA; VT; WA; WI; WV; WY; AB; BC; MB; NB; NF; NS; ON; PE; QC; SK; Mexico
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nearly worldwide; especially in warm temperate regions |
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Discussion | Subspecies 2 (2 in the flora). Orobanche uniflora forms a polymorphic complex that requires more detailed study. The detection of broad-scale patterns of morphological variation is confounded by the differentiation among local races. D. M. Achey (1933) recognized five varieties, and K. C. Watson (1975), in her unpublished thesis, revised the classification to three subspecies. The present treatment, which accepts only the two major infraspecific variants as subspecies, should be considered highly tentative. (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. 472. | FNA vol. 17, p. 456. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Orobanchaceae > Orobanche | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | Anoplanthus uniflorus, Aphyllon uniflorum, Thalesia uniflora | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | Linnaeus: Sp. Pl. 2: 633. (1753) | Ventenat | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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