Potentilla anserina |
Potentilla biennis |
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common silverweed, Pacific cinquefoil, silver weed cinquefoil, silverweed |
biennial cinquefoil, biennial or Greene's cinquefoil, Greene's cinquefoil |
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Stems | ascending to erect, (1–)2–6(–8.5) dm, hairs at base not stiff, not tubercle-based, glands sparse to abundant, conspicuous (to 1 mm, septate). |
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Leaves | ternate, (2–)4–12(–25) cm; petiole (1–)2–8(–20) cm, long hairs sparse to common, spreading to ascending, 0.5–1.5(–3) mm, weak, crisped hairs usually absent, glands sparse to abundant, conspicuous (to 1 mm, septate); leaflets 3, at tip of leaf axis, usually overlapping, largest ones mostly obovate or oval to nearly round, (0.5–)1–3(–4) × 0.3–3(–3.5) cm, distal 3/4 to ± whole margin evenly to unevenly incised 1/4–1/3(–1/2) to midvein, teeth 3–8(–13) per side, surfaces sparsely to moderately hairy, rarely glabrate, glands sparse to abundant at least abaxially. |
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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). |
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Inflorescences | (10–)20–70+-flowered. |
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Pedicels | 0.2–1(–2) 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 oblanceolate to narrowly obovate or elliptic, (1.5–)2–3.5(–4.5) × 0.5–1.5(–2) mm; hypanthium (2–)3–4(–5.5) mm diam.; sepals (2–)3–5 mm, apex broadly acute to obtuse; petals pale yellow to yellow, broadly oblanceolate to obovate, (1–)2–2.7 × 1.5 mm; stamens 10 or 15, filaments 0.5–1.2 mm, anthers 0.2–0.3 mm; carpels 40–100, styles 0.5–0.7 mm. |
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Achenes | 2 mm. |
whitish or pale yellowish, 0.5–0.9 mm, smooth, without a corky protuberance. |
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Potentilla anserina |
Potentilla biennis |
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Phenology | Flowering summer. | |||||||||||||
Habitat | Moist meadows, stream banks, ditches, seepages | |||||||||||||
Elevation | 400–3100 m (1300–10200 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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AK; AZ; CA; CO; ID; MT; ND; NM; NV; OR; UT; WA; WY; AB; BC; SK; YT
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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 biennis may be recognized by its septate hairs with a round, terminal gland, which dominate the vestiture especially at the base of the plant. Stems are more commonly erect and leaflets rounder than those of P. rivalis. The species is most common along the eastern side of the Sierra Nevada of California, across the Intermountain Region to the Rocky Mountains. All specimens seen by the authors from Baja California, Mexico, which were previously referred to P. biennis are now assigned to P. rivalis. J. Soják (1996) lectotypified Potentilla millegrana Engelmann ex Lehmann upon a collection of P. rivalis, thus preventing P. biennis from being a later taxonomic synonym. (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. 140. | ||||||||||||
Parent taxa | Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Pentaphylloides | Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Rivales | ||||||||||||
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Synonyms | Argentina anserina | |||||||||||||
Name authority | Linnaeus: Sp. Pl. 1: 495. (1753) | Greene: Fl. Francisc., 65. (1891) | ||||||||||||
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