Eriophyllum lanosum |
Eriophyllum |
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white Easter bonnets, white easterbonnets or woolly daisy, white woolly daisy |
woolly sunflower |
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Habit | Annuals, 3–15 cm. | Annuals, perennials, subshrubs, or shrubs, 1–200 cm. | ||||||||||||||||||||||||||||||||||||||||||||||||
Stems | decumbent to ascending. |
erect or decumbent, usually branched (proximally, distally, or ± throughout). |
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Leaves | blades oblanceolate to linear, 5–20 mm, rarely lobed, ultimate margins, usually entire, plane (apices acute), faces sparsely woolly. |
mostly cauline; mostly alternate (proximal sometimes opposite); petiolate or sessile; blades usually 1–2(–3)-pinnately lobed, ultimate margins toothed, serrate, or entire, faces usually densely to sparsely woolly (abaxial or both, adaxial sometimes glabrescent). |
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Peduncles | 1–5 cm. |
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Involucres | campanulate to obconic, 3–5 mm diam. |
campanulate to hemispheric, 3–12+ mm diam. |
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Receptacles | flat or convex to conic, smooth or pitted, glabrous, usually epaleate (with 1–6 hyaline paleae in E. ambiguum, obscurely setose in E. mohavense). |
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Ray florets | 8–10; laminae white with red veins, 3–5 mm. |
0, or 4–13(–15), pistillate, fertile; corollas yellow or white (sometimes with reddish veins in E. lanosum). |
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Disc florets | 10–20; corollas 2–3 mm (tubes cylindric, throats funnelform, gradually dilated, lobes glandular; anther appendages subulate, not glandular). |
(3–)10–300, bisexual, fertile; corollas yellow, tubes shorter than or about equaling funnelform throats, lobes 5, deltate. |
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Phyllaries | 8–10, distinct. |
persistent, 4–13(–15) in 1+ series (± erect in fruit, distinct or basally connate, lanceolate to oblanceolate, herbaceous or indurate, slightly to deeply concave, usually carinate, margins sometimes scarious, abaxial faces densely to sparsely woolly). |
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Heads | borne singly. |
radiate or discoid, borne singly or in loose to tight, corymbiform or compound-corymbiform arrays. |
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Cypselae | 2.5–4.5 mm; pappi of 5 subulate scales 1.5–2.5 mm plus 4–5 oblong scales ± 0.5 mm. |
linear-clavate to prismatic, flattened or 3-angled in rays, 4(–5)-angled in discs, hairy or glabrous; pappi 0, or persistent, of 6–12+ (distinct) erose to laciniate or aristate scales (in 1–2 similar or contrasting series), or ± coroniform. |
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x | = 8. |
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2n | = 8. |
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Eriophyllum lanosum |
Eriophyllum |
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Phenology | Flowering Feb–May. | |||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Sandy or gravelly openings, desert scrublands | |||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 70–1400 m (200–4600 ft) | |||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
AZ; CA; NM; NV; UT; Mexico (Baja California)
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w North America; nw Mexico |
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Discussion | Species 13 (13 in the flora). Eriophyllum encompasses taxa that occur in seashore, chaparral, grassland, desert, forest, and alpine communities. Their disparateness encouraged taxonomic multiplication. Between 1890 and 1937, about 157 designations under the genus existed (L. Constance 1937). Constance reduced that taxonomic thicket to six annual and five perennial species; the perennial species E. lanatum consisted of ten varieties. Base diploid chromosome numbers for Eriophyllum (in the sense of Constance) species are x = 4, 5, and 7 for the annuals, and x = 8, 15, and 19 for the perennials (S. Carlquist 1956; J. S. Mooring 1997, 2001, 2002). Possibly, x = 15 and x = 19 represent paleopolyploidy. Only E. mohavense remains uncounted. B. G. Baldwin (1999) linked Mooring’s (1997) report of n = 19 in E. nevinii to chromosomal, morphologic, and rDNA evidence, and erected the genus Constancea on that species. Eriophyllum (in the sense of Constance) seems most closely related to the annuals Pseudobahia (x = 3, 4, 8) and Syntrichopappus (x = 6, 7). Eriophyllum (in the sense of Baldwin), Pseudobahia, and Syntrichopappus constitute a clade, and nomenclatural changes are necessary for a monophyletic classification (Baldwin and B. L. Wessa 2000; Baldwin et al. 2002). Mooring (1997) hypothesized a descending dysploidy phylogeny in Eriophyllum (in the sense of Constance) from E. nevinii. Baldwin et al. (2002, p. 174) stated that E. nevinii “is an evolutionary outlier (although probably not ancestral) to” Eriophyllum in the sense of Constance. Natural intertaxon hybrids have been reported for the perennial species (L. Constance 1937; J. S. Mooring 1994) but not for the annuals. Experimental hybridizations have produced sterile hybrids between the annual E. congdonii and the perennial E. lanatum. Experimental crosses among seven of the annual species produced fertile hybrids between two morphologically similar species; the other combinations either failed or produced sterile hybrids (Mooring 2002). D. P. Tibor (2001) cited nine taxa of Eriophyllum as rare or endangered: the perennials E. confertiflorum var. tanacetiflorum, E. jepsonii, E. latilobum, E. (Constancea) nevinii, and E. lanatum vars. hallii and obovatum, and the annuals E. congdonii, E. mohavense, and E. nubigenum. Here, accounts of the annuals are by D. E. Johnson, the perennials by J. S. Mooring. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 21, p. 355. | FNA vol. 21, p. 353. | ||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | Asteraceae > tribe Heliantheae > subtribe Baeriinae > Eriophyllum | Asteraceae > tribe Heliantheae > subtribe Baeriinae | ||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | Burrielia lanosa, Antheropeas lanosum | |||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | (A. Gray) A. Gray: Proc. Amer. Acad. Arts 19: 25. (1883) | Lagasca: Gen. Sp. Pl., 28. (1816) | ||||||||||||||||||||||||||||||||||||||||||||||||
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