Potentilla anserina |
Potentilla arenosa |
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common silverweed, Pacific cinquefoil, silver weed cinquefoil, silverweed |
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Habit | Plants scarcely to ± tufted. | |||||||||||||||||
Caudex branches | thick, not columnar, not sheathed with marcescent whole leaves. |
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Stems | ascending to erect, (0.3–)0.8–2.5(–4.5) dm, lengths (2–)3–5 times basal leaves. |
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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). |
1.5–12(–20) cm; petiole 1–7(–15) cm, long hairs sparse to abundant, spreading to ± ascending, rarely loosely appressed, 1–2(–2.5) mm, usually stiff, sometimes weak (subsp. chamissonis), verrucose, short and/or crisped hairs absent or sparse to abundant, cottony hairs absent, glands absent or sparse; leaflets separate to ± overlapping, central obovate, 1–3.5(–4.5) × 0.5–2(–3) cm, usually petiolulate, petiolule to 5 mm, base cuneate, margins slightly revolute, distal ± 3/4 incised ± 1/2 to midvein, teeth (2–)3–4(–6) per side, ± approximate to distant, surfaces dissimilar, often strongly so, abaxial white to gray, long hairs 0.5–1.8 mm, cottony-crisped hairs ± dense, adaxial green, sometimes grayish green, long hairs sparse to abundant, short-crisped hairs sparse to abundant. |
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Cauline leaves | (0–)1–2. |
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Inflorescence | 1–7(–15)-flowered. |
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Pedicels | 1.5–5 cm in flower, to 6(–10) cm in fruit. |
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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 linear-lanceolate to lanceolate-elliptic, 2–5(–7) × 0.4–1.2(–1.5) mm, 1/4–1/2 as wide as sepals, margins usually flat, red glands absent or sparse and inconspicuous; hypanthium 3–5 mm diam.; sepals 3–6(–8) mm, apex acute; petals 4–7(–10) × 4–7(–9) mm, ± longer than sepals; filaments 0.8–1 mm, anthers 0.4 mm; carpels 28–40, apical hairs absent, styles conic-columnar, strongly papillate-swollen in proximal 1/5–1/3, 1–1.5 mm. |
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Achenes | 2 mm. |
1.1 mm. |
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Potentilla anserina |
Potentilla arenosa |
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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; AB; BC; MB; NT; NU; QC; SK; YT; Eurasia |
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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.) |
Subspecies 2 (2 in the flora). The name Potentilla arenosa is now used for most arctic and subarctic plants previously treated as P. hookeriana or P. nivea subsp. hookeriana (Lehmann) Hiitonen. As noted by J. Soják (1986), the type of P. hookeriana has quinate leaves; that name is now restricted to a Rocky Mountain species in sect. Rubricaules. The arctic and subarctic material was briefly (1989–1999) called P. nivea, as discussed under that species. Because the type of P. nivea var. arenosa and other northern Asian specimens correspond closely to the North American plants, the name P. arenosa is assigned here. The two subspecies differ only in one character, the petiole hairs, but are largely allopatric. Subspecies arenosa occurs in western and northern Greenland, northern North America (very northern in the east), and northern Asia (and perhaps northeasternmost European Russia); subsp. chamissonis occurs in southern Greenland, northeastern North America (more southern than subsp. arenosa), and northern Europe at least east to the Urals. (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. 200. | ||||||||||||||||
Parent taxa | Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Pentaphylloides | Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Niveae | ||||||||||||||||
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Synonyms | Argentina anserina | P. nivea var. arenosa | ||||||||||||||||
Name authority | Linnaeus: Sp. Pl. 1: 495. (1753) | (Turczaninow) Juzepczuk: in V. L. Komarov et al., Fl. URSS 10: 137. (1941) | ||||||||||||||||
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