Erigeron formosissimus |
Erigeron grandiflorus |
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beautiful fleabane |
large-flower daisy, large-flower fleabane, onestem fleabane, Rocky Mountain alpine fleabane |
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Habit | Perennials, 10–40(–55) cm; rhizomatous, fibrous-rooted, rhizomes variably thick. | Perennials, 2–25 cm; rhizomatous, fibrous-rooted, caudices or rhizomes crownlike or branches relatively short and thick. | ||||
Stems | ascending, densely hirsute to hirsutulous or glabrous, minutely glandular to stipitate-glandular. |
erect to decumbent-ascending, sparsely to moderately pilose to villoso-hirsute, often stipitate-glandular over all or part. |
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Leaves | basal (persistent) and cauline; basal blades oblanceolate to oblanceolate-spatulate, 20–100(–150) × 4–10(–15) mm, margins entire, closely ciliate, faces glabrous or sparsely hirsute, sometimes sparsely glandular; cauline blades becoming ovate to lanceolate, gradually reduced distally (bases clasping). |
basal (persistent) and cauline (petioles equaling or shorter than blades); blades oblanceolate to obovate or spatulate, 10–60(–90) × 3–8(–14) mm, cauline abruptly or gradually reduced distally, margins entire (apices rounded), faces sparsely hirsutulous or villous to sparsely strigose or glabrate, sometimes sparsely glandular. |
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Involucres | 5–8 × 10–20 mm. |
5–8(–10) × 8–20 mm. |
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Ray florets | 75–150; corollas blue to purple, rarely pink to white, 8–15 mm (ca. 1 mm wide), laminae coiling at tips or not at all. |
50–130; corollas blue to pink or purplish, rarely white, 7–11(–15) mm (mostly 1–2 mm wide), laminae coiling. |
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Disc corollas | 3.5–4.5 mm. |
2.4–4(–5) mm. |
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Phyllaries | in 2–3 series (greenish), glabrous or hirsuto-villous, densely minutely glandular to stipitate-glandular (glands sometimes obscured by hairs in var. formosissimus). |
in 2–3 series (green or purplish), moderately to densely woolly-villous (hairs flattened, cross walls sometimes reddish), minutely glandular at least apically. |
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Heads | 1–6. |
1. |
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Cypselae | (1.3–)1.6–1.9 mm, 2-nerved, faces sparsely strigose; pappi: outer of setae, inner of 15–25 bristles. |
1.8–2.4 mm, 2-nerved, faces strigose; pappi: outer of setae, inner of (7–)10–18(–22) bristles. |
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2n | = 18, 27. |
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Erigeron formosissimus |
Erigeron grandiflorus |
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Phenology | Flowering Jul–Aug(–Sep). | |||||
Habitat | Rocky sites, meadows, alpine or near timberline | |||||
Elevation | 2900–4200 m (9500–13800 ft) | |||||
Distribution |
AZ; CO; NM; SD; UT; WY
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AZ; CO; ID; MT; NM; OR; UT; WY; AB; BC
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Discussion | Varieties 2 (2 in the flora). Variation in vestiture of Erigeron formosissimus is complex, ranging from stems and heads glabrous and densely stipitate-glandular to stems and heads densely hairy and essentially eglandular; intermediates are found over the range of the species. The taxonomic solution of recognizing broadly sympatric varieties within a single species is biologically untenable, and some have treated this as a single entity; the variation is greater than typically occurs within a single species of Erigeron (see comments following 3. E. neomexicanus, where the situation with E. oreophilus is similar). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
S. A. Spongberg (1971) recognized only the triploid populations as Erigeron grandiflorus and assigned the diploid ones to E. simplex. He hypothesized that the triploids incorporate genomic elements from an ancestor other than E. simplex. Based on his comments and annotations, however, triploids in southern Canada and the western United States apparently differ from the much more widespread diploids only quantitatively, having involucres and florets at the higher end of size ranges. Morphologic distinctions between the ploidal races do not provide a basis for consistent distinction. Spongberg (p. 200) also noted that “because of the intergrading of morphologic features of plants of Erigeron grandiflorus...the single most important criterion indicative of this taxon is highly irregular [in shape] and greatly abortive pollen.” These pollen features result from meiotic anomalies associated with the triploid condition. Specimen citations by A. Cronquist (1947) for Erigeron grandiflorus were mostly from collections of the species treated here as E. porsildii. He also cited two collections from southwestern Alberta; those and the type collection of E. grandiflorus (from the same region) are disjunct by more than 1500 kilometers from the more northern range of E. porsildii and instead lie at the northern extremity of the range of what previously has generally been identified as E. simplex. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 20, p. 334. | FNA vol. 20, p. 324. | ||||
Parent taxa | Asteraceae > tribe Astereae > Erigeron | Asteraceae > tribe Astereae > Erigeron | ||||
Sibling taxa | ||||||
Subordinate taxa | ||||||
Synonyms | E. simplex | |||||
Name authority | Greene: Bull. Torrey Bot. Club 25: 121, plate 332, figs. 3, 4. (1898) | Hooker: Fl. Bor.-Amer. 2: 18, plate 123. (1834) | ||||
Web links |