Potentilla subjuga |
Potentilla villosula |
|
---|---|---|
Colorado cinquefoil |
Alaska cinquefoil, finely villous cinquefoil |
|
Habit | Plants densely tufted. | |
Caudex branches | stout, sometimes ± columnar, not sheathed with marcescent whole leaves. |
|
Stems | (0.8–)1–2.5(–3.5) dm. |
ascending to erect, 0.2–1.5(–2) dm, lengths 1.5–3(–4) times basal leaves. |
Basal leaves | usually palmate with additional lateral leaflets, sometimes pinnate, 3–10(–14) cm; petiole 1.5–5 cm, vestiture seasonally dimorphic, long hairs abundant, spreading on first-formed leaves, tightly appressed to ascending on later-formed leaves, 1–2 mm, ± stiff (especially on later-formed leaves), cottony and crisped hairs usually absent, glands absent or sparse; leaflets (3–)5 at tip of leaf axis plus 1(–2) additional pair(s) separated from tip by 3–20 mm, on distal 1/10–1/3(–1/2) of leaf axis, largest leaflets oblanceolate-oblong, (0.5–)1.5–2.5(–3) × 0.3–1 cm, ± whole margin incised 1/2–2/3(–3/4) to midvein, teeth (2–)4–9 per side, usually touching to strongly overlapping, sometimes separate, 2–6 mm, surfaces usually strongly dissimilar (less so on first-formed leaves), abaxial usually white, straight hairs ± abundant (mostly on veins), 1–2 mm, cottony or crisped/cottony hairs ± dense (sparser on first-formed leaves), glands absent or obscured, adaxial green (to grayish), straight hairs sparse to common, 0.5–1.5 mm, cottony and crisped hairs absent, glands sparse. |
1–5.5(–7) cm; petiole 0.5–3.5(–5) cm, long hairs common to dense, ascending to spreading, loosely appressed, sometimes retrorse, 1–2(–3) mm, soft, smooth, crisped/short-cottony hairs usually sparse, sometimes common, glands absent or sparse to common or obscured; leaflets overlapping, central broadly obovate to obtriangular, 0.8–2.5 × 0.6–2 cm, sessile to subsessile, base broadly cuneate, margins revolute, distal 1/2–2/3(–3/4) incised ± 1/2 to midvein, teeth 2–3(–4) per side, ± approximate to ± distant, surfaces ± dissimilar, abaxial grayish to white or yellowish white, long hairs 1.5–2.5 mm, cottony-crisped hairs ± dense, adaxial grayish green, long hairs abundant to dense, crisped hairs absent, sparse, or obscured. |
Cauline leaves | 1–3. |
(0–)1–2(–3). |
Inflorescences | 3–20(–30)-flowered. |
(1–)2–3(–4)-flowered. |
Pedicels | 0.5–2 cm (proximal to 3 cm). |
0.5–3(–5) cm in flower, to 4(–6) cm in fruit. |
Flowers | epicalyx bractlets narrowly to broadly lanceolate, 2–5(–6) × 1–1.5 mm; sepals 4–7 mm, apex acute to acuminate; petals 4–8 × 4–8 mm; filaments (0.5–)1–2 mm, anthers 0.3–0.8 mm; carpels 15–30, styles filiform to filiform-tapered, ± papillate-swollen in less than proximal 1/5, 1.5–2 mm. |
epicalyx bractlets broadly lanceolate to narrowly ovate, 3–7(–8) × 1.5–3(–3.5) mm, 2/3 to as wide as sepals, margins ± revolute, red glands absent; hypanthium (3–)4–6 mm diam.; sepals 4–7(–8) mm, apex acute or rarely acuminate; petals 5–10 × 6–12 mm, significantly longer than sepals; filaments 1.1–1.4 mm, anthers 0.5–0.8 mm; carpels 40–70, apical hairs absent or sparse (straight), styles narrowly columnar to conic-tapered, papillate-swollen in proximal 1/5 or less, 1–1.2 mm. |
Achenes | 1.2–1.6 mm. |
0.9–2 mm. |
2n | = 28 (Russian Far East). |
|
Potentilla subjuga |
Potentilla villosula |
|
Phenology | Flowering summer. | Flowering late spring to summer. |
Habitat | Alpine tundra and meadows, boulder piles, gravelly slopes, stabilized talus | Rocky alpine heaths, outcrops, scree and talus, gravel outwash plains, dry tundra, coastal bluffs, stabilized sand dunes, mostly on acidic bedrock |
Elevation | 3400–4000 m (11200–13100 ft) | 0–2900 m (0–9500 ft) |
Distribution |
CO; NM; AB
|
AK; AB; BC; YT; e Asia (Russian Far East) |
Discussion | Potentilla subjuga is centered in the high mountains of Colorado and barely enters New Mexico in the Sangre de Cristo Mountains. Collections from Alberta also apparently belong to this species, but all known collections from Wyoming have been identified as different taxa, at least one currently undescribed. At its most distinctive, P. subjuga is easily recognized by its unique leaf division, with five palmate leaflets subtended by an additional pair (or two) of lateral leaflets. Southern populations, however, are more likely to have only three apical leaflets. The leaflets tend to be strongly bicolored with overlapping teeth, in contrast to most sympatric pinnate species. Petiole vestiture is also distinctive in being seasonally dimorphic, with long hairs on first-formed leaves spreading to ascending and those on later formed leaves tightly appressed, as well as more conspicuously verrucose. Unresolved infraspecific variation exists, and field observations suggest that P. subjuga readily hybridizes with sympatric species, creating a swarm of intermediate specimens. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Potentilla villosula was included previously in P. villosa; the two overlap in the southern and western Alaskan coasts, where a transition is suspected to be associated with differing ploidy levels. The plants from this area with silky hairs and multiflowered inflorescences are assigned to P. villosa; P. villosula has thicker, stiffer, and less silky hairs, fewer teeth per leaflet, narrower bracts, fewer and smaller flowers with narrower epicalyx bractlets and sepals, and fewer achenes (sometimes with single apical hairs). While P. villosa is restricted to relatively rocky sites near the coast from western Alaska to Oregon, P. villosula often occurs on coastal sand dunes, farther inland, and/or farther to the north. As circumscribed, Potentilla villosula is a major plant of Alaska, especially of the Bering Sea region. The species extends from Alaska and the Yukon to at least central British Columbia. Most of the range given by E. Hultén (1968) for P. villosa belongs to P. villosula. W. J. Cody (1996) accepted the name P. villosula for a common south-central Yukon plant, but the majority of the plants mapped by Cody probably belong to P. subgorodkovii (although the distinction between the two species needs more resolution). Provisionally included here are plants from southern and central Yukon south through the Canadian Rockies, possibly including the type of P. nivea subsp. fallax A. E. Porsild. Such plants tend to be significantly smaller overall than Alaskan P. villosula; at least some have straight hairs on carpel apices. J. Soják (2004) believed that Potentilla villosula evolved from crosses between P. villosa and P. vulcanicola. The affinity with P. villosa is seen in the sericeous vestiture, number of leaflet teeth, and flower number and size, and with P. vulcanicola in the frequent occurrence of straight hairs on carpel apices in both species. Plants with columnar caudex branches, representing a significant part of the Alaskan material, have been called subsp. congesta. This morphology results from the persistence of marcescent whole leaves for several years (in typical P. villosula only sheaths and petioles are retained). This character suggests that P. subvahliana, with which the form called subsp. congesta is sympatric, may be part of its parentage. Potentilla villosula is accepted here in a fairly collective sense, possibly including several hybrid lineages, but with P. villosa a part of them all. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 9, p. 166. | FNA vol. 9, p. 202. |
Parent taxa | Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Subjugae | Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Niveae |
Sibling taxa | ||
Synonyms | P. osterhoutiana | P. villosula subsp. congesta |
Name authority | Rydberg: Bull. Torrey Bot. Club 23: 397, plate 274. (1896) | Jurtzev: in A. I. Tolmatchew, Fl. Arct. URSS 9(1): 319. (1984) |
Web links |