Herbertia lahue |
Iridaceae |
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prairie nymph |
iris family |
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Habit | Plants (6–)8–15(–24) cm. | Herbs, perennial, rarely annual [or shrubs with woody caudex], evergreen or seasonal, sometimes cespitose; rootstock a rhizome, bulb, or corm. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bulbs | (10–)15–20 mm diam. |
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Stems | simple or 1–3 branched, branching usually from base. |
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Flowering stems | aerial (or subterranean in Romulea), simple or branched, terete or variously compressed, angled or winged. |
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Leaves | 4–6, mostly basal, ± reaching base of inflorescence, cauline leaves often entirely sheathing; blade ± linear, 4–6 mm wide. |
basal and cauline, distichous; proximal 2–3 sometimes membranous, not reaching much above ground; others with open or closed sheaths, usually unifacial [bifacial or terete], oriented edgewise to the stem; blade parallel-veined, plane or pleated, channeled. |
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Inflorescences | umbellate, monochasial cymes (rhipidia), spikes, or solitary flowers; rhipidia enclosed in 2, opposed, usually large, leafy to dry bracts (spathes); flowers except for the first subtended by 1 floral bract; spike flowers each subtended by 2, opposed bracts. |
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Flowers | usually pedicellate [± sessile]; perianth actinomorphic or zygomorphic, petaloid, with 2 equal or unequal whorls of 3 tepals each [1 whorl of 6]; tepals usually large, showy, distinct or connate in tube; stamens 3 [2], inserted at base of outer tepals or in tube, symmetrically arranged or unilateral, arcuate [declinate]; filaments distinct or partly to completely connate, sometimes weak, unable to support anthers; anthers with 2 pollen sacs, extrorse, occasionally latrorse, usually dehiscing longitudinally [rarely apically]; ovary inferior [superior in Tasmanian Isophysis], 3-locular [1-locular]; placentation axile [parietal]; ovules 2–few, anatropous; style single, filiform at least proximally, usually 3-branched or 3-lobed, branches either filiform, distally expanded, sometimes each divided in distal 1/2, stigmatic toward apices, or branches thickened, or flattened, petaloid, stigmas then abaxial below apices. |
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Fruits | capsular, loculicidal, rarely indehiscent, firm to cartilaginous, occasionally woody. |
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Capsules | ovoid–oblong-truncate, 15–25 mm. |
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Seeds | ca. 2.5 mm. |
globose to angular (prismatic) or discoid, sometimes broadly winged; seed coat usually dry (rarely fleshy); endosperm hard, with reserves of hemicellulose, oil, and protein; embryo small. |
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Rhipidia | (1–)2–5-flowered; outer spathe ca. 2/3 to ± equaling inner, inner (35–)40–50 mm, apex becoming dry. |
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Tepals | bluish purple to violet; outer spreading, lanceolate, 23–28 × 15–18 mm, flaccid, claws white at base, speckled with violet, 6–7 mm; inner violet, darkest on claws, ca. 8–12 × 3 mm; filament column ca. 5 mm; anthers recurving soon after dehiscence, 7–10 mm; ovary oblong, 5–7 mm; style branches 5–6 mm, forked apically for ca. 2.5 mm. |
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Herbertia lahue |
Iridaceae |
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Phenology | Flowering mid Mar–early May. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Woodlands and prairies, most common near coast | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
FL; LA; TX; South America (Argentina, Brazil, Chile, Uruguay)
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Nearly worldwide but rare in tropical lowlands; best represented in southern Africa |
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Discussion | Herbertia lahue is probably introduced in Florida. The taxonomy of Herbertia lahue has been much confused. Plants from North America were originally treated as H. caerulea, separate from the South American members of the genus. P. Ravenna (1968) regarded differences between this and two South American species, H. lahue and H. amoena, as trivial and not sufficient to allow anything more than infraspecific separation. He considered plants from northern Argentina to be indistinguishable from those from North America and united them under subsp. caerulea. Without ennumerating their differences, Ravenna treated plants from coastal southern Brazil, Uruguay, and Argentina with slightly smaller flowers as subsp. amoena (Grisebach) Goldblatt, and those from Chile as subsp. lahue. The variation in North American populations makes it impossible to maintain even subspecies in H. lahue on the basis of available information. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Genera ca. 65, species ca. 1810 (16 genera, 92 species; 9 genera, 19 species introduced, and various hybrid complexes in the flora). Iridaceae are currently divided into four subfamilies (P. Goldblatt 1990, 1991). Subfamily Isophysidoideae Takhtajan is monotypic, comprising the Tasmanian Isophysis T. Moore with a superior ovary. Only subfamily Iridoideae is native in North America. The remaining Nivenioideae Schulze ex Goldblatt and Ixioideae Klatt are centered in Africa south of the Sahara. Iridaceae are of considerable economic importance in ornamental horticulture and the cut-flower industry, especially Iris, Gladiolus, and Freesia. Several other genera (e.g., Crocus, Dietes, Sparaxis, Tritonia, Watsonia) are cultivated in gardens in both tropical and temperate areas. Moraea and Homeria are poisonous and pose significant problems in cattle- and sheep-raising areas, notably in southern Africa. In addition to the several genera and species escaped from cultivation and dealt with in detail below, the following are widely grown in areas of mild winter and may persist in and near abandoned gardens, sometimes reproducing successfully: Dietes Salisbury [D. iridioides (Linnaeus) Salisbury ex Klatt, D. grandiflora N. E. Brown]; Ixia Linnaeus (I. maculata Linnaeus, I. polystachya Linnaeus); Crocus cultivars and even some wild species. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 26, p. 397. | FNA vol. 26, p. 348. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Iridaceae > Herbertia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Synonyms | Ferraria lahue, Alophia lahue, Alophia lahue subsp. caerulea, Cypella drummondii, H. caerulea, H. drummondiana, H. lahue subsp. caerulea, H. watsonii, Iris brachystigma, Trifurcia caerulea, Trifurcia lahue, Trifurcia lahue subsp. caerulea | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | (Molina) Goldblatt: Ann. Missouri Bot. Gard. 64: 379. (1978) | Jussieu | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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