Draba santaquinensis |
Draba glabella |
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golden Draba, rock whitlow-grass, smooth Draba, smooth whitlow-grass, smooth whitlow-mustard |
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Habit | Biennials or perennials; (short-lived); caudex simple (poorly developed, without persistent leaf bases); not scapose. | Perennials; (sometimes cespitose); caudex simple or branched; not scapose. |
Stems | usually branched, 1.1–3.4 dm, hirsute proximally, trichomes mostly simple and 2-rayed, 0.2–1.5 mm, pubescent distally, trichomes mostly 2- or 3-rayed, 0.2–1 mm. |
branched or unbranched, (0.4–)1–3.5(–4.7) dm, often pubescent throughout (sometimes sparsely so distally), sometimes glabrous, trichomes simple and 2-rayed, (non-crisped), 0.2–1 mm, or subsessile, stellate-pectinate, and 3–8-rayed, 0.1–0.3 mm. |
Basal leaves | rosulate; petiole (obscure), ciliate, (trichomes simple and 2-rayed); blade obovate to oblanceolate, 1.6–2.5 cm × 5–10 mm, margins usually entire, rarely denticulate, surfaces pubescent, abaxially with stalked, mostly cruciform trichomes, 0.5–1 mm, adaxially with simple and stalked, 2–4-rayed ones. |
rosulate; petiolate; petiole ciliate, (trichomes simple, 0.1–0.8 mm); blade oblanceolate to spatulate or linear-oblanceolate, (0.6–)1–3.5(–5) cm × 2–8(–10) mm, margins dentate or denticulate, (pubescent as petiole), surfaces pubescent with non-crisped, minutely stalked, 4–8(–12)-rayed, stellate-pectinate trichomes, 0.15–0.6 mm, (midvein obscure abaxially), adaxially sometimes also with simple trichomes, or glabrous. |
Cauline leaves | usually 1–5; sessile or subsessile; blade oblanceolate to oblong, margins often denticulate, (ciliate proximally, with 2- or 3-rayed trichomes). |
2–17(–25); sessile; blade ovate to oblong, margins dentate to subentire, surfaces often pubescent as basal, or predominantly with simple trichomes adaxially. |
Racemes | 9–25-flowered, ebracteate, elongated in fruit; rachis not flexuous, pubescent, trichomes 2- or 3-rayed. |
(5–)8–26(–34)-flowered, ebracteate or proximalmost 1 or 2 flowers bracteate, elongated in fruit; rachis not flexuous, usually glabrous, rarely pubescent as stem. |
Flowers | sepals oblong-obovate, 2–3.5 mm, pubescent, (trichomes short- to long-stalked, 2–4-rayed, 0.2–0.8 mm); petals yellow (often fading whitish), oblanceolate, 3–5 × 1–1.5 mm; anthers ovate, 0.4–0.5 mm. |
sepals oblong, 2–3.5 mm, pubescent, (trichomes simple and short-stalked, 2–4-rayed); petals white, broadly obovate, 4–5.5 × 1.5–3 mm; anthers ovate, 0.3–0.5 mm. |
Fruiting pedicels | horizontal to divaricate-ascending, usually straight, rarely curved upward, 7–10 mm, pubescent, trichomes 2- or 3-rayed. |
divaricate-ascending to suberect, straight, (1–)3–10(–16) mm, glabrous or pubescent as stem. |
Fruits | narrowly elliptic to slightly falcate, plane, flattened, (7–)10–16 × (2–)2.5–3.7 mm; valves pubescent, trichomes short-stalked, 2–4-rayed, 0.2–0.5 mm; ovules 14–22 per ovary; style 0.9–1.2 mm. |
oblong to ovate or ovoid to lanceolate or linear-lanceolate, usually plane, rarely slightly twisted, flattened or inflated, (3–)5–12(–16) × 2–3.5 mm; valves glabrous or pubescent, trichomes simple or 2–4-rayed, 0.05–0.2(–0.4) mm; ovules (20–)24–36 per ovary; style 0.05–0.2(–0.5) mm. |
Seeds | oblong, 1.1–1.5 × 0.7–0.9 mm. |
oblong, 0.9–1.1 × 0.5–0.7 mm. |
2n | = 20. |
= 64, 80. |
Draba santaquinensis |
Draba glabella |
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Phenology | Flowering late Apr-early Jun. | Flowering May–Aug. |
Habitat | Limestone outcrops and rocky slopes in mixed conifer communities | Rock outcrops, talus, rocky ridges and knolls, meadows, tundra, gravelly beaches sandy river margins, disturbed soils |
Elevation | 1800-2400 m (5900-7900 ft) | 0-1400 m (0-4600 ft) |
Distribution |
UT |
AK; ME; VT; WI; BC; MB; NB; NL; NS; NT; NU; ON; QC; YT; Greenland; n Europe (n Russia); e Asia (Russian Far East, Siberia) |
Discussion | Although Draba santaquinensis was included within D. brachystylis by previous authors, I. A. Al-Shehbaz and M. D. Windham (2007) have shown that it is distinct both morphologically and chromosomally. It is currently known only from Utah County (American Fork, Provo, and Santaquin canyons) in north-central Utah. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Draba glabella was reported by J. V. Freudenstein and J. K. Marr (1986) from Michigan, but that record likely was based on plants of D. arabisans, a highly variable species that occurs in that state. Draba glabella is extremely variable in indumentum, number of cauline leaves, fruiting pedicel length, fruit shape and size, style length, and seed number. M. L. Fernald (1934) divided it into five species and three varieties; R. C. Rollins (1993) recognized three species. Of these, G. A. Mulligan (1970, 1976) reduced D. laurentiana to synonymy of D. glabella and treated D. pycnosperma as a variety. Of all the segregates of D. glabella, var. pycnosperma might merit recognition. It is restricted to northwestern Newfoundland and northeastern Quebec, where var. glabella also grows. The main difference between the two varieties is the presence in var. pycnosperma of plump (versus flattened), ovoid to oblong fruits. Draba sornborgeri, recognized by Rollins as a distinct species, is merely a glabrescent form of D. glabella. Because of the tremendous morphological variability, wide distribution, extensive synonymy, and different chromosome numbers, D. glabella will require extensive molecular, cytological, and morphological studies to properly delimit the species and any potential infraspecific taxa. Some forms of Draba glabella approach both D. borealis and D. praealta, but these can be distinguished by examining the trichomes on the abaxial surfaces of basal leaf blades. In D. glabella, these trichomes are minutely stalked or subsessile and have branched rays. In the other two species, the trichomes have long stalks and the rays are always unbranched. The Linnaean name Draba hirta was applied to this species previously, and still is in Russia. The name is not typified, and the material at LINN is in bad condition and probably belongs to two species, D. glabella and D. norvegica, as recognized here. A typification of D. hirta may necessitate its re-introduction for this species. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 7, p. 334. | FNA vol. 7, p. 307. |
Parent taxa | ||
Sibling taxa | ||
Synonyms | D. arabisans var. canadensis, D. arabisans var. orthocarpa, D. canadensis, D. canadensis var. pycnosperma, D. daurica, D. glabella var. megasperma, D. glabella var. orthocarpa, D. glabella var. pycnosperma, D. henneana, D. hirta var. laurentiana, D. hirta var. pycnosperma, D. laurentiana, D. megasperma, D. norvegica var. pleiophylla, D. pycnosperma, D. sornborgeri | |
Name authority | Windham & Allphin: Harvard Pap. Bot. 12: 410. (2007) | Pursh: Fl. Amer. Sept. 2: 434. (1813) |
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