Eurybia |
Eurybia furcata |
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aster |
fork aster |
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Habit | Perennials, 10–120 cm (rhizomes long and slender to short and thick, sometimes cormoid, often becoming woody). | Plants (30–)50–120 cm; strongly in clones or scattered clumps, eglandular; rhizomes elongate, fleshy. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stems | ascending to erect, usually simple, rarely branched proximally, glabrous or ± densely hairy, usually eglandular, sometimes stipitate-glandular. |
1–5+, erect, simple, ± flexuous distally (± ridged from decurrent leaf bases), glabrate proximally, sparsely villous distally. |
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Leaves | basal and cauline; alternate; sessile or petiolate; blades cordate, ovate, obovate, elliptic, or oblong to spatulate, oblanceolate, or lanceolate, usually gradually reduced distally, margins entire or serrate, sometimes spinulose-serrate, faces glabrate to hairy, usually eglandular, sometimes stipitate-glandular. |
basal and cauline (grayish green abaxially), bases often oblique, margins serrate, veins prominent, abaxial faces scabrous, adaxial hirsute; basal and proximal cauline withering by flowering (rosettes produced in late season, absent in spring), short-petiolate, petioles winged, sheathing, blades ovate-lanceolate, 40–130 × 20–90 mm, bases rounded to subcordate, apices obtuse to acute; mid short-petiolate, narrowly winged, wings revolute, bases dilated, sheathing, ciliate, blades ovate to lance-ovate, 100–120(–150) × (30–)60–80 mm, gradually reduced distally, bases shallowly cordate or truncate to rounded, margins sharply serrate, teeth mucronate, apices acuminate; distal (arrays) subpetiolate or sessile, ovate, 8–70 × 4–23 mm, bases sheathing or clasping. |
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Peduncles | 0.5–3(–5) cm, villous; bracts 0–3. |
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Involucres | cylindro-campanulate to broadly campanulate, (4–14(–16) ×) 4–25+ mm. |
campanulate, 6–8(–10) mm, much shorter than pappi. |
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Receptacles | flat to slightly convex, pitted, epaleate. |
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Ray florets | 5–60, pistillate, fertile; corollas white to purple (coiling at maturity). |
(12–)15–20; corollas white, sometimes becoming pink or lavender, 12–18 × 1–2.5 mm. |
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Disc florets | 8–260, bisexual, fertile; corollas yellow, becoming purple at maturity, barely to abruptly ampliate, tubes shorter to longer than funnelform to campanulate throats, lobes 5, usually erect to spreading, sometimes ± reflexed, deltate, triangular, or lanceolate; style-branch appendages lanceolate. |
25–35+; corollas cream or light yellow becoming purple, 6–7(–8) mm, slightly ampliate, tubes cylindric, lengths about twice funnelform throats, lobes erect, lanceolate, 0.8–1.2 mm (glabrous). |
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Phyllaries | 20–140 in 3–7 series, 1-nerved (usually rounded adaxially, sometimes low-keeled), broadly ovate or oblong to oblanceolate, lanceolate, or linear, unequal, bases indurate (rarely wholly foliaceous), margins narrowly scarious (seldom herbaceous), often ciliolate (green zones ± basally truncate), in distal 1/3–3/4 of phyllary (outer) to less than 1/6 and only along midnerves (inner), apices obtuse to acute, faces glabrous, ± strigillose, puberulent, scabrellous, strigoso-villous, or villous, sometimes ± stipitate-glandular. |
ca. 40 in 5 series, oblong (outer) to linear-lanceolate (inner), strongly unequal, membranous, bases indurate and low-keeled or rounded abaxially, green zones in distal 1/4–1/3, obovate, poorly defined, margins hyaline, scarious, villoso-ciliate, inner often purplish, apices appressed, obtuse to rounded, faces villous, eglandular. |
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Heads | radiate, usually in corymbiform arrays, rarely borne singly. |
4–32+ in flat-topped, corymbiform arrays. |
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Cypselae | cylindro-obconic to fusiform, ± compressed, 7–12(–18)-nerved, faces glabrous or sparsely to densely strigillose, eglandular; pappi persistent, of 35–70+, reddish, orange, cinnamon, tawny, tan, yellowish, or pinkish, unequal, soft to stiff, barbellate or barbellulate, often apically ± clavate bristles in 2–4 series. |
brown, fusiform, (2.5–)3–3.5(–4) mm, ribs 8–10(–12), crowded, stramineous to tan, faces ± strigillose; pappi of tawny (apically sometimes clavellate) bristles 6–7 mm, equaling or slightly shorter than disc corollas. |
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x | = 9. |
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2n | = 18. |
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Eurybia |
Eurybia furcata |
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Phenology | Flowering late Jul–Oct. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Calciphile, ± open habitats (± shade intolerant), limestone, sandstone and dolomite areas, mostly n-facing slopes, seepy bluffs, moist deciduous woods, especially along streams, sometimes disturbed sites | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 200–600 m (700–2000 ft) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
North America; n Eurasia |
AR; IA; IL; IN; MI; MO; WI
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Discussion | Species 23 (23, including 1 hybrid, in the flora). Eurybia traditionally has been treated within Aster in a broad sense. G. L. Nesom (1994b), in his review of North American asters, showed that Aster in a broad sense does not form a natural group and proposed splitting it into several genera, among which Eurybia is one. In his treatment, Nesom included Herrickia within Eurybia, as sect. Herrickia in subg. Eurybia. Such views were generally supported in molecular phylogenetic studies (J. C. Semple et al. 2002). L. Brouillet et al. (2004) showed, however, that Oreostemma, Herrickia, Eurybia, and Triniteurybia form a grade at the base of the Machaerantherinae and that Herrickia and Eurybia are distinct. The subgenera and sections proposed by G. L. Nesom (1994b), based on anterior taxonomy, could not be confirmed in the molecular studies cited above. I chose not to use subgeneric limits as proposed by Nesom because they may not reflect actual relationships. For instance, there is a clear gradation between members of sect. Calliastrum (Torrey & A. Gray) G. L. Nesom (subg. Eurybia) and sect. Heleastrum (de Candolle) G. L. Nesom. Also, I do not recognize sect. Eryngiifoliae (Alexander) G. L. Nesom distinct from sect. Heleastrum, as there is no clear demarcation between the two as currently defined. Finally, sect. Radulini (Rydberg) G. L. Nesom appears artificial to me, but currently there is no good way to reassign its species. The Eurybia radulina complex of western North America clearly constitute a group, but it is unclear whether the western E. conspicua or the eastern E. radula and E. saxicastelli are close to them. Members of other sections may have played a role in the reticulate evolution of sect. Eurybia, even though it is well marked by its cordate leaves and disc florets with long tubes and short, campanulate corollas. Therefore, species are described below in a rough taxonomic order, with diploids listed before polyploids of the same group. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
D. H. Les et al. (1991b) studied the population genetics of this restricted taxon, and Les et al. (1992) its distribution and autecology in Wisconsin. J. A. Reinartz and D. H. Les (1994) showed that the species is developing self-compatibility in response to small populations. Eurybia furcata is uncommon throughout its range and is considered endangered or threatened in all states where it occurs; it is known only from historic records in Arkansas. It is in the Center for Plant Conservation’s National Collection of Endangered Plants. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 20, p. 365. | FNA vol. 20, p. 372. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms | Aster subg. E. | Aster furcatus | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | (Cassini) Cassini: in F. Cuvier, Dict. Sci. Nat. ed. 2, 16: 46. (1820) | (E. S. Burgess) G. L. Nesom: Phytologia 77: 259. (1995) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Web links |