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

hairy cinquefoil, northern cinquefoil, villous cinquefoil

Habit Plants ± to densely tufted.
Caudex branches

stout, sometimes short-columnar, not sheathed with marcescent whole leaves.

Stems

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

ascending, 0.5–2(–2.5) dm, lengths 1.5–3 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.

2–12(–15) cm;

petiole 1–9(–12) cm, long hairs ± abundant to dense, spreading to ascending, 1–2.5(–3) mm, soft to weak, smooth, crisped hairs absent or sparse, cottony hairs absent, glands sparse to common, sometimes obscured;

leaflets usually ± overlapping, central broadly obovate to suborbiculate, (0.5–)1.5–2.5(–3) × (0.5–)1.5–2.6(–3.2) cm, sessile to subsessile, base cuneate to rounded, margins revolute, distal 1/2–2/3(–3/4) incised 1/4–1/2 to midvein, teeth 3–6(–7) per side, ± approximate to ± distant, surfaces ± dissimilar, abaxial yellowish or grayish white, long hairs 1–2 mm, cottony-crisped hairs ± dense, adaxial grayish green, long hairs abundant to dense, crisped hairs absent, sparse, or obscured.

Cauline leaves

1–2(–3).

(0–)1–2.

Inflorescences

10–30-flowered.

(1–)2–7(–10)-flowered.

Pedicels

0.3–3(–5) cm.

0.5–3(–4) cm in flower, to 4 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 ovate to oval-elliptic, 3–8 × 2–5 mm, 2/3 to as wide as sepals, margins strongly revolute, red glands absent;

hypanthium 5–7 mm diam.;

sepals 4–8 mm, apex ± acute;

petals (5–)7–15 × 7–16 mm, significantly longer than sepals;

filaments 1.8–2.1 mm, anthers 0.7–0.8 mm;

carpels 150–250, apical hairs usually absent, rarely present (cottony), styles narrowly conic to tapered, ± papillate-swollen on proximal 1/5–1/2, 0.9–1.1 mm.

Achenes

1.4–1.8 mm, smooth to faintly rugose.

0.9–1.3 mm.

2n

= 42, 70, 77, 84, 98.

= 14.

Potentilla hippiana

Potentilla villosa

Phenology Flowering summer. Flowering spring–summer.
Habitat Dry grasslands and meadows, in aspen and conifer woodlands or alpine tundra, disturbed sites Sea cliffs, gravel beaches, inland on alpine outcrops (primarily southern populations), pumice barrens, scree and rock ledges
Elevation 500–3400 m (1600–11200 ft) 0–100(–1800) m (0–300(–5900) 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; OR; WA; BC; e Asia (Russian Far East)
[WildflowerSearch map]
[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.)

Potentilla villosa is the only documented diploid species of sect. Niveae in North America and, almost certainly, it is fully sexual. It is a characteristic species of coarse-grained beaches and coastal cliffs from southwestern British Columbia to western Alaska and the Russian Far East, and also occurs on scattered mountains in the Olympic Peninsula and Cascade Range of Washington and Oregon (providing the higher elevational extreme). These southern populations, which have been called var. parviflora, tend to be smaller, more delicate, less hairy plants in general, with fewer and smaller flowers. At least some plants in some southern populations also have cottony hairs on the carpels.

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

Source FNA vol. 9, p. 162. FNA vol. 9, p. 201.
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. 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. villosula, P. vulcanicola, P. wheeleri
Synonyms P. leucophylla, P. argyrea, P. effusa var. argyrea, P. hippiana var. argyrea, P. hippiana var. diffusa, P. propinqua P. villosa var. parviflora
Name authority Lehmann: Nov. Stirp. Pug. 2: 7. (1830) — not Pallas 1773 Pallas ex Pursh: Fl. Amer. Sept. 1: 353. (1813)
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