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Hipp's cinquefoil, horse cinquefoil, potentille de Hipp, woolly cinquefoil

Beringian cinquefoil, yurtsev's cinquefoil

Habit Plants ± densely tufted.
Caudex branches

stout, usually columnar, sometimes sheathed with marcescent whole leaves.

Stems

(0.3–)2–4(–5) dm, lengths (1–)2–4 times basal leaves.

erect, (0.2–)0.3–1.5(–2) dm, lengths 1.5–2.5(–3.5) times basal leaves.

Basal leaves

pinnate to subpinnate, (3–)5–15(–25) cm;

petiole 1–10(–15) cm, long hairs abundant to dense, tightly appressed, 1–2.5 mm, stiff, short hairs absent or obscured, crisped-cottony hairs absent or sparse to common, glands absent or obscured;

leaflets not conduplicate, lateral ones evenly (to unevenly in argyrea phase) paired, (2–)3–6(–7) per side on distal (1/6–)1/5–1/2 of leaf axis, distal pairs ± decurrent, often confluent with terminal leaflet, larger leaflets oblanceolate or narrowly obovate to oblong, 1–5(–6) × 0.3–1.5 cm, distal (2/3–)3/4 to whole margin incised 1/2 or less (rarely more) to midvein, teeth (5–)7–12(–18) per side, 1–4 mm, surfaces ± to strongly dissimilar, abaxial white, long hairs abundant (mostly on, but not limited to, veins), 1–2 mm, stiff, short hairs absent or obscured, crisped-cottony hairs abundant to dense, glands absent or obscured, adaxial green to grayish, long hairs sparse to common, rarely absent, short or crisped to, sometimes, cottony hairs absent or sparse to common, glands sparse.

(1–)2–10(–15) cm;

petiole (0.5–)1–5(–12) cm, long hairs common to dense, ± ascending to loosely appressed, sometimes spreading, 1–2 mm, ± soft, smooth, crisped/short-cottony hairs usually sparse, sometimes absent or common, glands absent, sparse, or obscured;

leaflets separate to slightly overlapping, central obovate or obtriangular, (0.5–)1–2(–3) × (0.4–)0.8–1.5(–2) cm, sessile or subsessile, base cuneate, margins revolute, distal (1/3–)1/2–2/3(–3/4) incised 1/2–2/3(–3/4) to midvein, teeth 2–3(–4) per side, usually ± distant, surfaces somewhat to more often strongly dissimilar, abaxial yellowish or grayish white to white, long hairs 0.8–1.5 mm, cottony-crisped hairs ± dense, adaxial green to grayish green, long hairs sparse to ± abundant, other hairs usually absent.

Cauline leaves

1–2(–3).

(0–)1(–2).

Inflorescences

10–30-flowered.

usually 1(–2)-flowered, rarely to 5-flowered.

Pedicels

0.3–3(–5) cm.

(0.5–)2–4 cm in flower, to 5 cm in fruit.

Flowers

epicalyx bractlets narrowly elliptic to lanceolate, rarely linear, 2–5 × 0.5–1.5 mm, (1/2–)2/3 as long as sepals, abaxial vestiture similar to or ± sparser than sepals, usually not glabrescent, straight hairs ± abundant, crisped to sometimes ± cottony hairs absent or sparse to abundant;

hypanthium 3–7 mm diam.;

sepals 4–5.5(–6.5) mm, apex acute to acuminate;

petals 4–8 × 4–7 mm;

filaments 0.5–2.5 mm, anthers 0.6–1.1 mm;

carpels (5–)10–30, styles 1.7–2.5 mm.

epicalyx bractlets elliptic-lanceolate to ovate, (3–)4–6(–7) × (0.8–)1.2–2(–2.5) mm, (1/2–)2/3 to as wide as sepals, margins revolute, rarely flat, red glands absent;

hypanthium 2.5–4 mm diam.;

sepals 4–6(–7) mm, apex subacute;

petals (5–)6–9 × (5–)7–9 mm, significantly longer than sepals;

filaments 1–1.3 mm, anthers 0.4–0.6 mm;

carpels 30–40, apical hairs absent, styles narrowly columnar to conic-tapered, papillate-swollen on proximal 1/5(–1/3), 0.9–1.1 mm.

Achenes

1.4–1.8 mm, smooth to faintly rugose.

1.2–2 mm.

2n

= 42, 70, 77, 84, 98.

= 28, 42, 49, 56 (Russian Far East).

Potentilla hippiana

Potentilla subgorodkovii

Phenology Flowering summer. Flowering late spring to summer.
Habitat Dry grasslands and meadows, in aspen and conifer woodlands or alpine tundra, disturbed sites Dry alpine heaths, exposed ridges and summits, rock outcrops, scree and talus, dry tundra, acidic and calcareous bedrock
Elevation 500–3400 m (1600–11200 ft) 0–4300 m (0–14100 ft)
Distribution
from FNA
AZ; CO; ID; MI; MN; MT; ND; NE; NM; NV; SD; UT; WY; AB; BC; MB; NS; NT; ON; QC; SK
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; CO; MT; UT; WY; AB; BC; NT; NU; YT; Asia (Russian Far East, Sakha [Yakutia])
[BONAP county map]
Discussion

Potentilla hippiana is most common and distinctive in the Colorado Plateau and southern Rocky Mountains, with outliers in the mountains of Arizona, Nevada, and New Mexico. Occurrences are more scattered in the northern Rocky Mountains and Great Plains, where intergradation with P. effusa is common. Among these intermediates are the argyrea phase and the single report from Idaho (B. C. Johnston 1980). Potentilla hippiana is probably adventive in Nova Scotia, eastern Ontario, Quebec, and Michigan, and possibly the Northwest Territories. The reported occurrence in central Alaska (E. Hultén 1968) is based on a specimen of P. pensylvanica (CAN).

Significant variation exists throughout the range of Potentilla hippiana, including dwarfism, leaf division, leaflet dissection, adaxial leaflet vestiture, and pedicel length. Some of this variation might merit taxonomic recognition upon further analysis, especially if correlated with ploidy level (6x through 12x). At present, the differences used to distinguish var. argyrea are not found to be sufficiently correlated with distribution to merit formal taxonomic recognition.

Complicating the infraspecific variation is a tendency for Potentilla hippiana to intergrade with other species, in particular P. effusa. Beyond sect. Leucophyllae, the frequency of hybrids with P. pulcherrima blurs the distinction between the two species; P. gracilis var. hippianoides S. L. Welsh & N. D. Atwood is probably one of the resultant intermediates.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

The name Potentilla subgorodkovii was coined for a presumed hybrid species resulting from P. crebridens × P. subvahliana; here it is applied in a collective meaning for plants combining characteristics from multiple species of the P. uniflora/villosa and P. nivea groups. Morphologically, this collective entity is much closer to the P. uniflora/villosa group than to the P. nivea group and is clearly different from primary hybrids and clones, which are often observed.

Potentilla subgorodkovii constitutes about half of what previously has been considered P. uniflora in Alaska and Yukon and is the only such entity fully confirmed south of northern British Columbia. These southern populations occur outside the range of possible parental members of the P. uniflora/villosa group and do not support the hybrid hypothesis. They may instead represent a distinct species, not yet described.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Source FNA vol. 9, p. 162. FNA vol. 9, p. 204.
Parent taxa Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Leucophyllae Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Niveae
Sibling taxa
P. albiflora, P. ambigens, P. anachoretica, P. angelliae, P. anglica, P. anserina, P. arenosa, P. argentea, P. arizonica, P. basaltica, P. bicrenata, P. biennis, P. biflora, P. bimundorum, P. bipinnatifida, P. brevifolia, P. breweri, P. bruceae, P. brunnescens, P. canadensis, P. concinna, P. cottamii, P. crantzii, P. crebridens, P. crinita, P. cristae, P. demotica, P. drummondii, P. effusa, P. elegans, P. erecta, P. flabellifolia, P. fragiformis, P. furcata, P. glaucophylla, P. gracilis, P. grayi, P. hickmanii, P. holmgrenii, P. hookeriana, P. hyparctica, P. inclinata, P. intermedia, P. jepsonii, P. johnstonii, P. lasiodonta, P. litoralis, P. macounii, P. millefolia, P. modesta, P. morefieldii, P. multijuga, P. multisecta, P. nana, P. newberryi, P. nivea, P. norvegica, P. ovina, P. paucijuga, P. pedersenii, P. pensylvanica, P. plattensis, P. pseudosericea, P. pulchella, P. pulcherrima, P. recta, P. reptans, P. rhyolitica, P. rimicola, P. rivalis, P. robbinsiana, P. rubella, P. rubricaulis, P. sanguinea, P. saximontana, P. sierrae-blancae, P. simplex, P. sterilis, P. stipularis, P. subgorodkovii, P. subjuga, P. subvahliana, P. subviscosa, P. supina, P. thurberi, P. thuringiaca, P. tikhomirovii, P. townsendii, P. uliginosa, P. uschakovii, P. vahliana, P. verna, P. versicolor, P. villosa, P. villosula, P. vulcanicola, P. wheeleri
P. albiflora, P. ambigens, P. anachoretica, P. angelliae, P. anglica, P. anserina, P. arenosa, P. argentea, P. arizonica, P. basaltica, P. bicrenata, P. biennis, P. biflora, P. bimundorum, P. bipinnatifida, P. brevifolia, P. breweri, P. bruceae, P. brunnescens, P. canadensis, P. concinna, P. cottamii, P. crantzii, P. crebridens, P. crinita, P. cristae, P. demotica, P. drummondii, P. effusa, P. elegans, P. erecta, P. flabellifolia, P. fragiformis, P. furcata, P. glaucophylla, P. gracilis, P. grayi, P. hickmanii, P. hippiana, P. holmgrenii, P. hookeriana, P. hyparctica, P. inclinata, P. intermedia, P. jepsonii, P. johnstonii, P. lasiodonta, P. litoralis, P. macounii, P. millefolia, P. modesta, P. morefieldii, P. multijuga, P. multisecta, P. nana, P. newberryi, P. nivea, P. norvegica, P. ovina, P. paucijuga, P. pedersenii, P. pensylvanica, P. plattensis, P. pseudosericea, P. pulchella, P. pulcherrima, P. recta, P. reptans, P. rhyolitica, P. rimicola, P. rivalis, P. robbinsiana, P. rubella, P. rubricaulis, P. sanguinea, P. saximontana, P. sierrae-blancae, P. simplex, P. sterilis, P. stipularis, P. subjuga, P. subvahliana, P. subviscosa, P. supina, P. thurberi, P. thuringiaca, P. tikhomirovii, P. townsendii, P. uliginosa, P. uschakovii, P. vahliana, P. verna, P. versicolor, P. villosa, P. villosula, P. vulcanicola, P. wheeleri
Synonyms P. leucophylla, P. argyrea, P. effusa var. argyrea, P. hippiana var. argyrea, P. hippiana var. diffusa, P. propinqua
Name authority Lehmann: Nov. Stirp. Pug. 2: 7. (1830) — not Pallas 1773 Jurtzev: Bot. Zhurn. (Moscow & Leningrad) 78: 83. (1993)
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