Potentilla anserina |
Potentilla pedersenii |
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common silverweed, Pacific cinquefoil, silver weed cinquefoil, silverweed |
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Caudex branches | not sheathed with marcescent whole leaves. |
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Stems | ascending to nearly erect, 0.4–2 dm. |
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Basal leaves | petiole (0.5–)1–15(–25) cm, long hairs absent or sparse to dense, 1.5–3.5 mm; larger leaflets (0.4–)0.5–5(–7) × (0.2–)0.3–2(–3) cm, surfaces: abaxial with long hairs absent or sparse to abundant, not restricted to veins, 0.5–2(–2.5) mm, cottony-crisped hairs usually dense or usually absent (in subsp. groenlandica), adaxial with long hairs absent or sparse to abundant, cottony-crisped hairs usually absent, sometimes sparse to common (especially subsp. yukonensis). |
often both ternate and palmate or subpalmate on same plant, 2.5–4 cm; petiole 1.5–2.5 cm, long hairs common to abundant, loosely appressed to ascending-spreading, 1–2 mm, weak to ± stiff, verrucose, crisped(/short) hairs absent or sparse to common, cottony hairs absent, glands sparse to common; leaflets 3–5, proximalmost separated by 0–2 mm, central broadly elliptic to obovate, 1–1.5 × 0.5–0.9 cm, petiolules 1–2 mm, distal 2/3–3/4 of margin incised 1/2–3/4 to midvein, teeth (2–)3–4 per side, 4–6 mm, apical tufts ± 1 mm, abaxial surfaces grayish white to white, long hairs abundant (sometimes obscuring entire surface), cottony-crisped hairs abundant to dense, short hairs absent or obscured, glands sparse to common but usually obscured, adaxial grayish green to gray, long hairs sparse to abundant, 1–1.5(–2) mm, ± weak, short (short-crisped) hairs absent or sparse, rarely common, cottony hairs absent, glands absent or sparse, rarely common. |
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Cauline leaves | 0–2. |
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Inflorescences | (1–)3–7-flowered, open, branch angle 30–50°. |
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Pedicels | 1–2 cm, proximal to 4 cm. |
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Flowers | epicalyx bractlets narrowly to broadly ovate-triangular or linear to elliptic, (2–)2.5–7(–8) × (0.3–)0.5–3(–3.5) mm, often 2-fid or dentate; sepals (3–)3.5–7(–9) mm, apex subacute to acuminate; petals (4–)5–15(–20) × (2.5–)3–10(–12) mm; filaments (1–)2.5–3.5(–4.5) mm, anthers 0.7–1.3 mm; carpels (10–)20–200(–250). |
epicalyx bractlets narrowly ovate to elliptic, 4–5 × 1–1.4 mm; hypanthium 3–4 mm diam.; sepals 4–6 mm, apex subacute to acute, glands sparse to common, usually not obscured; petals pale yellow, usually not overlapping, 6–7 × 4–8 mm, distinctly longer than sepals; filaments 1–2 mm, anthers ± 0.4 mm; carpels 40–80, styles 0.8–0.9 mm. |
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Achenes | 2 mm. |
1.1–1.2 mm. |
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Potentilla anserina |
Potentilla pedersenii |
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Phenology | Flowering summer. | |||||||||||||
Habitat | Dry tundra, gravel and loam ridges, loam flats, rocky outcrops and crevices | |||||||||||||
Elevation | 0–200 m (0–700 ft) | |||||||||||||
Distribution |
AK; AZ; CA; CO; CT; IA; ID; IL; IN; MA; ME; MI; MN; MT; ND; NE; NH; NM; NV; NY; OH; OR; RI; SD; UT; VT; WA; WI; WY; AB; BC; MB; NB; NL; NS; NT; NU; ON; PE; QC; SK; YT; Mexico; South America (Argentina, Chile); Eurasia; Pacific Islands (New Guinea, New Zealand); s Australia
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NT; NU; Greenland; ne Europe; n Asia |
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Discussion | Subspecies 4 or 5 (4 in the flora). Potentilla anserina is polymorphic in most features, especially in hairiness, but also in size and in degree of dissection of leaflets, epicalyx bractlets, and sepals. While most of the variation described by A. G. Blytt (1906) is taxonomically insignificant, A. Rousi (1965) found support for three northern races: subspp. anserina, egedei, and pacifica. He also suggested that P. yukonensis Hultén might qualify as a separate subspecies. This treatment follows J. Soják (1994) in accepting four northern subspecies of P. anserina, all present in North America. A. Rousi (1965) demonstrated partial interfertility between the races of Potentilla anserina, which form intermediates in all zones of contact. The distinctness of the four races, in spite of intermediates, is upheld by being partly allopatric and occupying different habitats where they are sympatric. As partly interfertile parapatric entities, they are best treated as subspecies. The vast majority of chromosome counts are tetraploid. Tetraploid plants (2n = 28) are fully fertile; hexaploids (2n = 42) are largely pollen and seed sterile; pentaploids (2n = 35) are probably occasional hybrids (S. Erlandsson 1942, 1942b; A. Rousi 1965). A. Kurtto et al. (in J. Jalas et al. 1972+, vol. 13) considered numbers above tetraploid level as cases of occasional autopolyploidy. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Potentilla pedersenii and P. uschakovii account for the majority of arctic populations previously included in a broadly defined P. rubricaulis. The diagnostic morphological characters between the two species can be variable and overlapping; they are treated separately in part because of differences in presumed parental combinations. Whereas P. pulchella is the probable sect. Pensylvanicae parent for both species, the putative sect. Niveae parent for P. pedersenii is P. arenosa subsp. arenosa; that of P. uschakovii is P. subvahliana. Reflecting this parentage, P. pedersenii is distinguished by caudex branches with no marcescent whole leaves, verrucose long hairs on petioles, and inflorescences with usually several relatively small flowers. In contrast, P. uschakovii often has marcescent whole leaves sheathing the caudex branches, smooth long hairs on petioles, and one- or few-flowered inflorescences with mostly larger flowers. These generalities aside, there is much variation within both species, such that each island or population group may have its own features; it is probable that both P. pedersenii and P. uschakovii have evolved from multiple hybridization events. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 9, p. 127. | FNA vol. 9, p. 210. | ||||||||||||
Parent taxa | Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Pentaphylloides | Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Rubricaules | ||||||||||||
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Subordinate taxa | ||||||||||||||
Synonyms | Argentina anserina | P. subquinata var. pedersenii, P. tolmatchevii | ||||||||||||
Name authority | Linnaeus: Sp. Pl. 1: 495. (1753) | (Rydberg) Rydberg: in N. L. Britton et al., N. Amer. Fl. 22: 332. (1908) | ||||||||||||
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