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cut-leaf cinquefoil, feather cinquefoil, feather or many-leaf or Klamath cinquefoil, many leaf cinquefoil

potentille des neiges, snow cinquefoil, snowy cinquefoil

Habit Plants ± rosetted; taproots fleshy-thickened. Plants ± tufted.
Caudex branches

stout, not columnar, not sheathed with marcescent whole leaves.

Stems

usually prostrate, sometimes ± decumbent, 0.4–2(–3) dm, lengths 1–2 times basal leaves.

ascending to erect, (0.3–)0.5–3(–4) dm, lengths 1.5–2.5(–4) times basal leaves.

Basal leaves

pinnate with distal leaflets ± confluent, 2–15(–20) × 1–3 cm;

petiole 0.5–2(–3) cm, straight hairs sparse to abundant, appressed to spreading, 0.5–1.5 mm, stiff, cottony hairs absent, glands absent or sparse;

primary lateral leaflets (3–)5–13 per side, on distal 2/3–3/4+ of leaf axis, separate to overlapping, largest ones cuneate to flabellate, 0.5–1.5(–2) × 0.5–2 cm, distal 2/3 to whole margin palmately or unevenly, rarely pinnately, incised 2/3 to completely to midvein, ultimate teeth or segments (1–)2–10, linear to broadly oblanceolate, 2–10 × (0.5–)1–2 mm, apical tufts to 1 mm, surfaces green to grayish green, not glaucous, straight hairs sparse to abundant, appressed to spreading, 0.5–1.5(–2) mm, stiff, cottony hairs absent, glands sparse to common.

(1–)3–10(–15) cm;

petiole (0.5–)1–6(–10) cm, long hairs usually absent, sometimes sparse to common (less so than cottony hairs), ± appressed, 1–2 mm, soft, smooth, short-crisped hairs absent or obscured, cottony hairs abundant to dense sometimes sparse with age, glands absent, sparse, or obscured;

leaflets overlapping, central obovate, 0.5–2(–4) × (0.2–)0.4–1.2(–2) cm, subsessile, base cuneate, margins slightly revolute, distal ± 3/4 incised (1/4–)1/3–1/2 to midvein, teeth (2–)3–5(–6) per side, ± approximate, surfaces dissimilar, often strongly so, abaxial ± white, long hairs 0.8–1.2 mm, cottony-crisped hairs dense, adaxial usually green, sometimes grayish green, long hairs sparse to abundant, short-crisped hairs sparse to common.

Cauline leaves

(0–)1–2.

0–1.

Inflorescences

3–6(–10)-flowered, loosely cymose, sometimes racemiform.

1–5(–7)-flowered.

Pedicels

(0.5–)1–2(–4.5) cm, ± recurved in fruit.

1–4 cm in flower, to 5 cm in fruit.

Flowers

epicalyx bractlets ± elliptic, 2–4(–6) × 1–2(–2.5) mm;

hypanthium 3–6 mm diam.;

sepals 4–6(–8) mm, apex acute;

petals 4–8(–10) × 3–7(–9) mm;

filaments 2–3.5 mm, anthers 0.7–1 mm;

carpels 10–30, styles (1.5–)2–3 mm.

epicalyx bractlets narrowly to broadly lanceolate or elliptic, (2–)4–7 × 0.6–1.7 mm, usually 1/4–1/2 as wide as sepals, margins flat, red glands usually absent, sometimes sparse, inconspicuous;

hypanthium (2–)3–4 mm diam.;

sepals (2.5–)4–8 mm, apex acute;

petals (3–)4–8 × (3–)5–9 mm, slightly longer than sepals;

filaments 0.9–1.2 mm, anthers 0.5 mm;

carpels 20–40, apical hairs absent, styles narrowly columnar or columnar-tapered, strongly papillate-swollen at very base, rarely in proximal 1/5–1/3, 0.7–1.2 mm.

Achenes

1.5–2 mm, smooth, often ± carunculate.

1.1–1.5 mm.

2n

= 56, 63; 28, 42, 49, 70 (Asia, Europe).

Potentilla millefolia

Potentilla nivea

Phenology Flowering spring–summer. Flowering summer.
Habitat Vernally to permanently wet meadows, moist openings in conifer forests and sagebrush, alkaline flats Well-drained, exposed sites, ridge crests, coarse mineral soil, scree, usually on calcareous substrates
Elevation 700–2200 m (2300–7200 ft) 400–3800 m (1300–12500 ft)
Distribution
from FNA
CA; NV; OR
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; AZ; CO; MT; NM; UT; WA; WY; AB; BC; MB; NL; NT; NU; QC; YT; Greenland; Eurasia
[WildflowerSearch map]
[BONAP county map]
Discussion

Potentilla millefolia occurs from central Oregon to the east side of the Sierra Nevada of California, with a disjunct occurrence on the alkaline flats of Reese River Valley, Nevada. Significant variation occurs in vestiture type, leaflet dissection, and flower size, but with minimal geographic correlation. The most distinctive variant, represented by the type of P. klamathensis, has relatively long, slender, spreading, pustule-based hairs, often intermixed with shorter hairs. This vestiture type does not appear to be correlated with any other characters or geographic distribution and may vary within a population.

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

Although now restricted to plants with exclusively (or at least predominantly) cottony hairs on the petioles, the name Potentilla nivea has a long history with an often wider application, sometimes including nearly all of sect. Niveae. As further confusion, J. Soják (1989) noted that the Linnaean type of P. nivea belonged to what is here treated as P. arenosa. Although historical usage of P. nivea has been re-established as a conserved name with a conserved type (B. Eriksen et al. 1999), from 1989 to 1999 the name P. nivea was applied to P. arenosa. During this period, P. prostrata subsp. floccosa was briefly adopted as the correct name for this species (for example, W. J. Cody 1996).

Molecular evidence (B. Eriksen and M. H. Töpel 2006) indicates that populations of Potentilla nivea in the Atlantic regions, including Greenland and eastern Canada, differ from those in the Beringian regions of northwestern North America, suggesting expansion from separate Pleistocene refugia. A comparable pattern was noted by R. Elven and S. G. Aiken (2007) based on morphologic characters. The conserved type of P. nivea is from northern Sweden (Eriksen et al. 1999) and belongs to the Atlantic morphologic group. The variation within each region is large, and racial recognition would accordingly be premature. Plants from sites south of the continental glaciation, which were not included in the analysis by Eriksen and Töpel, deviate in having acuminate leaflet teeth and epicalyx bractlets and in being generally more slender. Epicalyx bractlets of some Washington plants are nearly as narrow as those of P. crebridens.

Additional chromosome numbers have been reported for Potentilla nivea, but it is unknown whether these apply to this species, P. crebridens, some Asian relative, or hybrids.

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

Source FNA vol. 9, p. 174. FNA vol. 9, p. 198.
Parent taxa Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Multijugae 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. hippiana, P. holmgrenii, P. hookeriana, P. hyparctica, P. inclinata, P. intermedia, P. jepsonii, P. johnstonii, P. lasiodonta, P. litoralis, P. macounii, 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. 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
Synonyms P. klamathensis, P. millefolia var. klamathensis, P. plattensis var. klamathensis, P. plattensis var. millefolia P. prostrata subsp. floccosa
Name authority Rydberg: Bull. Torrey Bot. Club 23: 433, plate 277, figs. 1–5. (1896) Linnaeus: Sp. Pl. 1: 499. (1753)
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