Braya humilis subsp. ellesmerensis |
Braya humilis |
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alpine northern-rockcress, dwarf braya, low braya, low northern-rockcress |
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Habit | Plants not scapose; sparsely to densely pubescent throughout, or, rarely, glabrescent, trichomes short-stalked or subsessile, submalpighiaceous or, rarely, 2-forked, often mixed along petioles and stem base with simple ones. | |||||||||||||
Stems | usually ascending (prostrate in fruit), unbranched, 0.3–1.6 dm, moderately pubescent. |
usually few to several from base, rarely simple, ascending or erect, rarely subdecumbent, (0.4–)0.8–2.5(–3.5) dm. |
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Leaves | blade margins pinnatifid or entire, surfaces moderately pubescent. |
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Basal leaves | blade obovate, spatulate, oblanceolate, oblong, or sublinear, (0.3–)0.5–2(–3.5) cm × 1–8(–10) mm, base attenuate or cuneate, margins entire, sinuate-dentate, or pinnatifid, apex acute or obtuse, (surfaces sparsely to densely pubescent or, rarely, glabrous). |
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Cauline leaves | 3 or more; blade similar to basal, smaller distally, distalmost sessile or subsessile. (Racemes bracteate proximally, very rarely throughout, elongated in fruit.) Fruiting pedicels erect, ascending, or divaricate, (2.5–)3–8(–12) mm. |
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Flowers | petals white or purple-tinged, (3–)4–5.6 × (1.3–)2–3.3(–3.8) mm. |
sepals 2–3 × 0.8–1.2 mm, (sometimes slightly saccate basally); petals white, pink, or purple, (broadly obovate or spatulate), 3–5(–8) × (1–)1.5–2.5(–4) mm, (apex rounded); filaments 2–3(–4) mm; anthers oblong, 0.4–0.7mm, (apex apiculate). |
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Fruits | usually fertile and fully developed, not or weakly torulose, (1–)1.2–1.8(–2) mm wide; septum often fenestrate (with circular perforations at regular intervals longitudinally or with a narrow, elliptical, longitudinal split at base or both). |
linear, torulose or not, (mostly straight), (0.9–)1.2–2.5(–3.2) cm × 0.6–1.8(–2) mm (uniform in width); valves pubescent or, rarely, glabrescent, trichomes submalpighiaceous, rarely mixed with fewer, simple ones; septum fenestrate or not; ovules 20–44 per ovary; style 0.3–0.8(–1) mm; stigma entire or strongly 2–lobed. |
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Seeds | uniseriate, oblong, 0.6–0.9x 0.4–0.5 mm. |
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2n | = 42. |
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Braya humilis subsp. ellesmerensis |
Braya humilis |
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Phenology | Flowering Jun–Jul, fruiting Jul–Aug. | |||||||||||||
Habitat | Sand, clay, and gravel slopes and plains | |||||||||||||
Elevation | 0-200 m (0-700 ft) | |||||||||||||
Distribution |
NU |
AK; CO; MI; MT; VT; WY; AB; BC; MB; NF; NT; NU; ON; QC; YT; e Asia; c Asia
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Discussion | Prostrate fruiting stems, exceptionally broad, non-torulose fruits, and fenestrate silique septae distinguish subsp. ellesmerensis from other subspecies of Braya humilis. It is known only from northern Ellesmere Island. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Subspecies 4 (4 in the flora). Braya humilis was recognized in Asian floristic accounts as a member of Neotorularia Hedge & J. Léonard (= Torularia O. E. Schulz), but molecular studies (S. I. Warwick et al. 2004) clearly support its assignment to Braya, as done by all North American authors (e.g., M. L. Fernald 1918; E. C. Abbe 1948; T. W. Böcher 1956, 1973; J. G. Harris 1985; R. C. Rollins 1993). The species is highly variable in leaf shape and margin, flower size and color, pubescence, fruit length and orientation, chromosome number, and length of the bracteate portion of the raceme. Occurrence of “races” with various ploidy levels is one of the reasons for variability that led to recognition of infraspecific taxa. The synonymy below pertains only to North America, with nearly as many names given to the Asian variants. Numerous morphological extremes were described in North America, Russia, and China, but most of those represent only part of an otherwise continuous variation. For example, fully bracteate racemes, though rare, appear sporadically in populations that otherwise have racemes only basally bracteate. Three morphological forms are more sharply distinct from the general subsp. humilis amalgam and seem to have some biological significance. All of them are restricted to areas in or near regions believed to have served as glacial refugia during the Pleistocene. They are recognized here as additional subspecies. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 7, p. 550. | FNA vol. 7, p. 548. | ||||||||||||
Parent taxa | ||||||||||||||
Sibling taxa | ||||||||||||||
Subordinate taxa | ||||||||||||||
Synonyms | Sisymbrium humile, Neotorularia humilis, Torularia humilis | |||||||||||||
Name authority | J. G. Harris: Novon 16: 345. (2006) | (C. A. Meyer) B. L. Robinson: in A. Gray et al., Syn. Fl. N. Amer. 1(1,1): 141. (1895) | ||||||||||||
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