Symphyotrichum novae-angliae |
Symphyotrichum jessicae |
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aster de nouvelle-angleterre, New England American-aster, New England aster, New England or michaelmas daisy |
Jessica's aster, Palouse aster |
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Habit | Perennials, 30–120 cm, cespitose; with thick, woody, branched caudices, or short, fleshy rhizomes, sometimes with woody cormoid portions. | Perennials, 40–150 cm, colonial; long-rhizomatous. |
Stems | 1–5+, erect (stout, light to dark brown, sometimes purplish distally), proximally sparsely to moderately hispiduloso-hirsute or pilose, distally moderately to densely so, stipitate-glandular. |
1–5+, ascending to erect, densely puberulent to lanate, especially distally. |
Leaves | (light to dark green) thin, often stiff, margins entire or sometimes with shallow teeth, ciliate; basal withered or withering by flowering, sessile, blades (3-nerved) usually spatulate, sometimes oblanceolate, 20–60 × 5–15 mm, bases attenuate, apices acute, faces sparsely hirsute; proximal cauline withering by flowering, sessile, blades oblong or lanceolate, 50–100 × 5–15(–20) mm, bases auriculate-clasping, margins entire, pustulate-scabrous, apices acute, mucronulate, faces stipitate-glandular, abaxial thinly strigose, adaxial hirsute or hispidulous; distal sessile, blades oblanceolate, 30–80 × 6–15 mm, gradually reduced distally, bases auriculate-clasping, apices acute to obtuse, mucronate to minutely white-spinulose, faces moderately to densely short-soft-hairy, sparsely to moderately stipitate-glandular. |
thickish, margins entire or shallowly crenate, apices acute to ± obtuse, faces densely lanate-puberulent; basal withering by flowering, petiolate, blades obovate to elliptic, 30–150 × 10–40 mm, bases cuneate to rounded, margins entire, ciliolate, apices acute, faces densely cinereous to lanate; proximalmost cauline sometimes withering by flowering, subpetiolate or sessile, blades obovate-lanceolate to elliptic, 50–100 × 10–25(–35) mm, bases cuneate, clasping, ± auriculate, apices usually acute; distal sessile, blades 20–60(–80) × 9–16(–20) mm, bases rounded to auriculate. |
Peduncles | dilated distally, 0.3–4 cm, densely short-hairy, stipitate-glandular, bracts 1–4, foliaceous, linear to narrowly lanceolate, densely short-hairy, stipitate-glandular, grading into phyllaries. |
densely lanate, bracts 1–8, elliptic, margins ciliolate, apices acute, puberulent. |
Involucres | campanulate to hemispheric, (5–)7–9(–15) mm. |
campanulate, 6–10 mm. |
Ray florets | (40–)50–75(-100); corollas dark rose to deep purple (pale pink or white), laminae 9–13 × 0.8–1.3 mm. |
18–40; corollas violet, laminae (8–)12–20 × 1–2(–2.5) mm. |
Disc florets | 50–110; corollas light yellow becoming purple, (4–)4.5–5.5(–7) mm, tubes ± 1/2 narrowly funnelform throats (glabrous or thinly puberulent), lobes triangular, 0.4–0.7 mm. |
35–80+; corollas yellow, 6–9 mm, lobes triangular, 0.4–1 mm. |
Phyllaries | in 3–5(–6) series (dark green to purple-tinged), linear-lanceolate, subequal, outer foliaceous, mid and inner scarious in basal 1/3–1/2, margins stipitate-glandular, apices long-acuminate to acuminate, spreading to reflexed or squarrose, faces glabrous, outer densely stipitate-glandular. |
in 4–6 series, oblanceolate (outer) to linear (inner), unequal, bases scarious (outer sometimes foliaceous), margins slightly scarious, entire, green zones obovate to elliptic, apices acute, faces densely lanate to cinereous. |
Heads | in leafy, often crowded, paniculo-corymbiform arrays. |
in paniculiform, very leafy arrays, branches 4–10(–20) cm. |
Cypselae | dull purple or brown, oblong or obconic, not compressed, 1.8–2.5(–3) × 0.6–1 mm, 7–10-nerved, faces densely sericeous, sparsely stipitate-glandular; pappi tawny (barb tips sometimes rose-tinged), 4.5–6 mm. |
brown, cylindric to obovoid, not compressed, 3.5–4.5 mm, 4–5-nerved, faces sparsely hairy; pappi tawny, (6–)7–9 mm. |
2n | = 10. |
= 80. |
Symphyotrichum novae-angliae |
Symphyotrichum jessicae |
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Phenology | Flowering Aug–Oct(–Nov). | Flowering Aug–Sep. |
Habitat | Open, moist to wet, sandy or loamy, rich soils, fields, prairies, meadows, marshy grounds, shrubby swamps, fens, shores, thickets, moist edges of woods, roadsides, railroad rights-of-way, somewhat weedy | Dry grasslands, meadows, stream banks, openings in Ponderosa pine woodlands |
Elevation | 0–1600 m (0–5200 ft) | 500–1200 m (1600–3900 ft) |
Distribution |
AL; AR; CO; CT; DC; DE; GA; IA; IL; IN; KS; KY; MA; MD; ME; MI; MN; MO; MS; MT; NC; ND; NE; NH; NJ; NM; NY; OH; OK; OR; PA; RI; SC; SD; TN; UT; VA; WA; WI; WV; WY; MB; NB; NS; ON; QC [Introduced in Europe]
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ID; WA
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Discussion | Symphyotrichum novae-angliae is escaped from cultivation and introduced in Montana, Oregon, Utah, Washington, and Wyoming, and has been reported as an ephemeral escape in British Columbia. It possibly escaped from cultivation elsewhere. The Michaelmas daisy is widely sold in the horticultural trade, where cultivars have been developed. Forms have been described that correspond to color genetic variants within natural populations {Aster novae-angliae forma roseus (Desfontaines) Britton; A. novae-angliae forma geneseensis House}; they are not recognized here. Symphyotrichum novae-angliae resembles Canadanthus modestus, but the ranges of the two do not overlap, and the latter has sparsely hairy cypselae with dark ribs. Symphyotrichum novae-angliae hybridizes with S. ericoides, forming the F1 intersectional hybrid S. ×amethystinum. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Of conservation concern. Symphyotrichum jessicae is known only from the Palouse and Clearwater river drainages of eastern Washington and adjacent northwestern Idaho. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 20, p. 487. | FNA vol. 20, p. 536. |
Parent taxa | Asteraceae > tribe Astereae > Symphyotrichum > subg. Virgulus | Asteraceae > tribe Astereae > Symphyotrichum > subg. Symphyotrichum > sect. Occidentales |
Sibling taxa | ||
Synonyms | Aster novae-angliae, Virgulus novae-angliae | Aster jessicae |
Name authority | (Linnaeus) G. L. Nesom: Phytologia 77: 287. (1995) | (Piper) G. L. Nesom: Phytologia 77: 283. (1995) |
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