Eurybia integrifolia |
Eurybia radulina |
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thick-stem aster |
rough-leaf aster, rough-leaf wood-aster |
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Habit | Plants 15–70 cm, usually in clumps, sometimes in large clones, densely long-stipitate-glandular distally; woody, branched, thick, usually short rhizomes or short caudices. | Plants 10–70 cm, laxly cespitose (grayish green), eglandular; rhizomes elongate, slender, woody. |
Stems | 1–3+, straight, stout, glabrous or sparsely hispid proximally, distally ± hispido-villous. |
1–3, ascending to erect, often purple, simple, flexuous, proximally glabrescent or sparsely villous, distally ± densely villous. |
Leaves | basal and cauline, firm, margins entire, strigoso-ciliate, distal also stipitate-glandular, apices mucronate, faces glabrous or glabrescent to ± densely hispid or strigose (then ± scabrous), particularly on veins, midveins sometimes notably hispido-villous, proximally ± sparsely, distally ± densely stipitate-glandular; basal and proximal cauline long-petiolate (to 100+ mm), petioles ± broadly winged, bases sheathing or auriculate-clasping, blades ovate-lanceolate to narrowly elliptic or oblanceolate, 33–180+ × 11–50 mm, bases attenuate, apices acute or obtuse to rounded; mid sessile, blades oblong or oblanceolate to oblong-lanceolate, lanceolate, or lance-ovate, 30–140 × 7–27 mm, gradually reduced distally, bases auriculate-clasping, apices usually acute, rarely obtuse; distal (arrays) narrowly ovate to lanceolate, 9–50 × 3–20 mm. |
cauline, firm, margins slightly revolute, coarsely serrate or (distal) entire, scabrous to strigoso-ciliate, teeth mucronate, ± markedly veined, apices mucronate, abaxial faces scabrous, adaxial scabroso-strigose; proximal mostly withering by flowering, petioles winged, shorter than blades, bases clasping, blades elliptic to obovate 12–45+ × 7–20+ mm, smaller than mid, apices obtuse; mid narrowly winged-petiolate (petioles short with ± clasping bases), distally subpetiolate or sessile, blades ovate or elliptic to broadly oblanceolate or obovate, 32–85(–130) × 4–40 mm, gradually reduced distally, bases usually attenuate, sometimes cuneate, apices obtuse to acute; distal (arrays) oblanceolate to lanceolate, 5–28 × 1–8 mm, more sharply reduced. |
Peduncles | ± densely long-stipitate-glandular; bracts 0(–2), densely stipitate-glandular. |
densely villous; bracts 0–1, scabroso-strigose. |
Involucres | campanulate, 8–14 mm, much shorter than pappi. |
campanulate, 6–9 mm, shorter than pappi. |
Ray florets | 8–27; corollas violet-purple, 10–15 × 1.2–2.2 mm. |
10–15; corollas white to sometimes pale violet or purple, 8.5–11(–13) × 1.3–2.3 mm. |
Disc florets | 20–50; corollas pale yellow turning pinkish or purplish, 6–7.8 mm, slightly ampliate, tubes much shorter than cylindric to narrowly funnelform throats, lobes erect, lanceolate, 0.6–0.8 mm. |
30–70; corollas yellow becoming purple- or pinkish-tinged, 6–7(–8) mm, ± ampliate, tubes equaling to longer than funnelform-campanulate throats, lobes usually erect, sometimes ± spreading, lanceolate, 1–1.3 mm. |
Phyllaries | 25–40 in 3–4 series, inner often purplish, oblong-lanceolate (outer) to linear-lanceolate (inner), ± unequal, membranous, bases pale, indurate, sometimes rounded (outer), distally foliaceous (3/4+ in outer, seldom to base, to 1/5 in inner) and wider than bases, margins narrowly scarious (non-foliaceous parts), purplish (at least inner), ciliate and/or stipitate-glandular (along foliaceous parts), apices squarrose, usually acute, sometimes acuminate, faces densely stipitate-glandular. |
38–62 in 4–5 series, midnerves slightly raised (outer), oblong (outer) to lanceolate-linear or linear (inner), unequal, membranous, bases indurate, ± rounded, green zones to scarious margins in distal 1/3–1/2 (outer; seldom ± wholly foliaceous) to 1/5 or none (inner), margins often purple, hyaline, narrowly scarious, erose, densely villoso-ciliate, apices appressed, sometimes purplish-tinged, usually acute, sometimes obtuse, adaxial faces villous. |
Heads | 3–41+ in elongate, racemo-corymbiform arrays, branches ascending. |
5–30+ in flat-topped, corymbiform arrays. |
Cypselae | greenish stramineous, fusiform-obconic, slightly compressed, 4.2–4.7 mm, ribs 7–10, faces ± densely hirtellous; pappi of stramineous to tawny bristles 7–8 mm, ± equaling disc corollas. |
tawny, fusiform, 3–3.5 mm, slightly compressed, ribs 7–9 (brown, translucent), faces strigillose; pappi of tawny bristles 2.7–3 mm, ± equaling disc corollas. |
2n | = 18. |
= 18, 27. |
Eurybia integrifolia |
Eurybia radulina |
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Phenology | Flowering summer–early fall. | Flowering summer. |
Habitat | Drier meadows, open, moist woodlands, in sedge-willow, sagebrush, Douglas fir, and spruce communities | Dry rock outcrops, edges of forests, open forests, mostly on slopes, foothill oak woodlands, oak, oak-fir, yellow pine forests |
Elevation | 1600–3200 m (5200–10500 ft) | (10–)100–1600 m ((0–)300–5200 ft) |
Distribution |
CA; ID; MT; NV; OR; UT; WA; WY
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CA; OR; WA; BC
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Discussion | Eurybia integrifolia is found in mountain ranges bordering the Basin and Range Province, from the Sierra Nevada and Cascade ranges in the west to the Rocky Mountains and Colorado Plateau in the east. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Eurybia radulina is confined mostly west of the Cascades, from southern Vancouver Island (British Columbia) to the southern Coast Ranges, north Channel Islands, and central Sierra Nevada in California. It often is confused with E. merita in the western, coastal states where both are found, though populations are rarely if ever sympatric, the former apparently thriving at lower elevations than the latter. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 20, p. 368. | FNA vol. 20, p. 369. |
Parent taxa | Asteraceae > tribe Astereae > Eurybia | Asteraceae > tribe Astereae > Eurybia |
Sibling taxa | ||
Synonyms | Aster integrifolius, Aster amplexifolius | Aster radulinus, Aster eliasii, Weberaster radulinus |
Name authority | (Nuttall) G. L. Nesom: Phytologia 77: 260. (1995) | (A. Gray) G. L. Nesom: Phytologia 77: 261. (1995) |
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