Euphrasia |
Euphrasia stricta |
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euphrasia, eyebright |
drug eyebright, euphraise dressée, stiff eyebright, strict eyebright, Tartary eyebright |
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Habit | Herbs, annual [perennial]; hemiparasitic. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stems | erect, not fleshy, retrorsely hairy. |
branched, rarely simple, to 30 cm; branches 1–5 pairs, from middle and distal cauline nodes; cauline internode length 0.5–2 times subtending leaves. |
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Leaves | cauline, opposite; petiole absent or nearly so; blade sometimes fleshy, not leathery, margins crenate, serrate, dentate, or incised. |
blade narrowly oblong to ovate-oblong, 2–9(–12) mm, margins serrate, teeth 1–3 pairs, apices subacute to aristate. |
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Inflorescences | terminal, subcapitate to diffuse spikes, flowers solitary in each axil; bracts present, subopposite or irregularly alternate. |
beginning at node (5–)7–9(–11); bracts green, sometimes purple adaxially, broader than leaves, oblong to ovate, length not more than 2 times width, 5–10 mm, surfaces glabrous or sparsely to densely hirsute and hairs eglandular, sometimes glandular-pubescent and hairs glandular, stalks 1- or 2-celled, 0.1–0.2 mm, teeth 4 or 5 pairs, longer than wide, apices acute, sometimes aristate. |
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Pedicels | present or absent; bracteoles absent. |
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Flowers | sepals 4, calyx bilaterally symmetric, not flattened laterally, tubular, not accrescent in fruit, lobes triangular; petals 5, corolla white or cream to purple, lilac, violet, brownish purple, or yellow with violet veins (often without violet veins in E. subarctica) and yellow spot in throat and on abaxial lip, adaxial lip sometimes lilac, purple, or yellow, contrasting with rest of corolla, bilabiate, funnelform, abaxial lobes 3, emarginate, adaxial 2, adaxial lip cucullate; stamens 4, didynamous, filaments glabrous, anther mucros unequal; staminode 0; ovary 2-locular, placentation axile; stigma capitate. |
corolla white, usually suffused with lilac, 8–10 mm, abaxial lip exceeding adaxial. |
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Capsules | dehiscence septicidal, opening in distal 1/2, margins ciliate, sometimes glabrous or short-ciliate (E. salisburgensis). |
narrowly oblong, 4.5–6 mm, apex truncate to retuse. |
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Seeds | 10–18, grayish, fusiform, wings absent. |
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x | = 11. |
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Euphrasia |
Euphrasia stricta |
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Distribution |
North America; South America; Eurasia; Africa (Morocco); Atlantic Islands (Azores, Iceland); Pacific Islands (Oceania); Australia |
IL; MA; ME; MI; MN; NH; NY; PA; RI; VT; WI; NB; NS; ON; PE; QC; Europe; Asia (w Siberia) [Introduced in North America]
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Discussion | Species ca. 350 (18 in the flora). Euphrasia is distributed throughout temperate regions of the northern and southern hemispheres, with one transtropical connection across the high mountains of Oceania. All Euphrasia species in the flora area belong to sect. Euphrasia, the largest of 15 sections in the genus (G. Gussarova et al. 2008). The section is noted for its taxonomic complexity. Major factors explaining the complex patterns of variation in sect. Euphrasia include interspecific hybridization, recent radiations, parasitism, polyploidization, and breeding system transitions (T. Karlsson 1974, 1986; P. F. Yeo 1978; G. C. French et al. 2008; R. A. Ennos et al. 2012). All North American species are tetraploids except, probably, E. disjuncta, E. farlowii, E. oakesii, E. randii, and E. subarctica. Of 18 species in the flora, nine are considered endemic. To facilitate identification of the species, the aggregate species concept is sometimes used to show relationships among the so-called more conventional, discrete taxa (Gussarova 2005). Following that concept, four aggregate species are represented in the flora area and their associated species treated here are: E. borealis (F. Townsend) Wettstein agg. (species 3 and 4), E. nemorosa agg. (species 6–10), E. oakesii agg. (species 13–15), and E. minima Jacquin ex de Candolle agg. (species 16 and 17). The key makes no provision for hybrids, which often have intermediate features or a mixture of character states typical of their putative parental species. For a reliable identification, multiple representative plants should be collected and examined from a population to account for individual variation in key characters. The bracts referred to in the key are proximal floral leaves, which are most representative of the variation along the stem. The teeth of the bracts become progressively more acute up the stem as well as on any one leaf from apex to base. To characterize teeth shape, the key uses the most basal ones. Sessile glands are often present on the abaxial surface of bracts; they have no taxonomic value. Glandular (on short versus long stalks) and eglandular hairs are used in characterizing indumentum of different species. Two infraspecific levels are used in this treatment. This is consistent with the usage in other Euphrasia treatments (for example, P. F. Yeo 1978). Subspecific rank is used for geographic or ecological integrity; varietal rank is used to indicate transitions between the extreme forms without any geographic or ecological distinction. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Varieties 7 (2 in the flora). Occurrence of Euphrasia stricta in Alberta is based on the report by G. C. D. Griffiths (2002); no specimen has been located. Griffiths listed E. arctica subsp. borealis as new for Alberta, but both morphological and habitat descriptions fit E. stricta more closely. If true, then this introduced species has crossed the continent; all earlier records are from eastern Canada and New England (S. R. Downie and J. McNeill 1988). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 17, p. 492. | FNA vol. 17, p. 496. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Name authority | Linnaeus: Sp. Pl. 2: 604. (1753): Gen. Pl. ed. 5, 263. (1754) | J. P. Wolff ex J. F. Lehmann: Prim. Lin. Fl. Herbipol., 43. (1809) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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