Eriophyllum wallacei |
Asteraceae tribe Heliantheae subtribe Baeriinae |
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Wallace eriophyllum, Wallace's woolly daisy, woolly daisy, woolly easterbonnets |
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Habit | Annuals, 1–15 cm. | Annuals, perennials, subshrubs, or shrubs, 1–200 cm. | ||||||||||||||||||||||||||||
Stems | erect to spreading or ascending. |
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Leaves | blades obovate to spatulate, 7–20 mm, sometimes 3-lobed, ultimate margins entire, plane (apices ± rounded), faces ± woolly. |
basal, basal and cauline, or mostly cauline; mostly opposite (Lasthenia) or mostly alternate; usually sessile, sometimes obscurely petiolate; blades (often 1–2 times pinnately lobed) or lobes often linear, ultimate margins entire or toothed, faces often ± woolly to tomentose, sometimes glabrate or glabrous, often gland-dotted. |
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Peduncles | 1–3 cm. |
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Involucres | broadly campanulate, 4–6 mm diam. |
ovoid or obconic to campanulate or hemispheric. |
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Receptacles | flat, convex, hemispheric, or conic (smooth, knobby, or pitted, glabrous or hairy), usually epaleate (paleae usually 0, rare in Eriophyllum). |
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Ray florets | 5–10; laminae usually cream or yellow, sometimes white with red veins, 3–4 mm. |
0 or 4–21, pistillate, fertile (3–8 peripheral florets pistillate, fertile, corollas tubular in Amblyopappus and Monolopia congdonii); corollas yellow to orange, often darker proximally, sometimes purplish (usually ± bilabiate in Monolopia). |
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Disc florets | 20–30; corollas 2–3 mm (tubes cylindric, throats funnelform, gradually dilated, lobes glandular; anther appendages subulate, not glandular). |
2–300, bisexual, fertile; corollas yellow to orange, tubes shorter than or about equaling funnelform or campanulate throats, lobes 4–5, deltate, glabrous or papillate; anther thecae usually pale; stigmatic papillae in 2 lines. |
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Phyllaries | 5–10, distinct. |
persistent, mostly 3–18 in 1–2 series, (erect or reflexed in fruit) distinct or connate, mostly elliptic, lanceolate, ovate, or obovate, usually ± equal, mostly herbaceous, sometimes indurate (at least proximally), flat or weakly cupped at bases, sometimes scarious-margined, often woolly to tomentose, sometimes glabrate or glabrous. |
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Calyculi | 0. |
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Heads | usually borne singly. |
radiate, discoid, or disciform, borne singly or in corymbiform, glomerate, or paniculiform arrays. |
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Cypselae | ± 2 mm; pappi usually of 6–10 ± oblong scales 0.4–0.8 mm, rarely 0. |
clavate or obovoid to terete, or obpyramidal, sometimes compressed or obcompressed, glabrous, hairy, or papillate (compressed, callous-margined, and ciliolate in Eatonella, Lasthenia chrysantha, and Monolopia congdonii; sometimes winged in Monolopia); pappi 0 or of 1–12+ aristate, erose, laciniate, or truncate scales or awns in 1–2 series (often 2 sorts of scales in combination on 1 cypsela). |
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2n | = 10 + 0–1 I or 0–3 B. |
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Eriophyllum wallacei |
Asteraceae tribe Heliantheae subtribe Baeriinae |
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Phenology | Flowering Dec–Jul. | |||||||||||||||||||||||||||||
Habitat | Sandy or gravelly openings, creosote-bush or sagebrush scrublands, Joshua Tree or pinyon-juniper woodlands, or chaparral | |||||||||||||||||||||||||||||
Elevation | 30–2400 m (100–7900 ft) | |||||||||||||||||||||||||||||
Distribution |
AZ; CA; NV; UT; Mexico (Baja California)
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w North America; Mexico; w South America |
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Discussion | Genera 9, species 44 (7 genera, 41 species in the flora). Members of Baeriinae are found mostly in western North America; there are disjuncts in western South America. H. Robinson (1981) treated Baeriinae as a relatively isolated element among epaleate subtribes of Heliantheae. B. G. Baldwin (in Baldwin et al. 2002) included Baeriinae within Madieae. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 21, p. 356. | FNA vol. 21, p. 335. | ||||||||||||||||||||||||||||
Parent taxa | Asteraceae > tribe Heliantheae > subtribe Baeriinae > Eriophyllum | Asteraceae > tribe Heliantheae | ||||||||||||||||||||||||||||
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Synonyms | Bahia wallacei, Antheropeas wallacei, E. wallacei var. rubellum | subtribe Eriophyllinae | ||||||||||||||||||||||||||||
Name authority | (A. Gray) A. Gray: Proc. Amer. Acad. Arts 19: 25. (1883) | Bentham & Hooker f.: Gen. Pl. 2: 200. (1873) | ||||||||||||||||||||||||||||
Web links |