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Brewer's cinquefoil

potentille des neiges, snow cinquefoil, snowy cinquefoil

Habit Plants rosetted to ± matted; taproots not fleshy-thickened. Plants ± tufted.
Caudex branches

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

Stems

prostrate to ascending, (0.5–)1–3(–4.5) dm, lengths 2–4(–5) 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–)4–12(–17) × 1–2.5(–5) cm;

petiole 1–3(–7) cm, straight hairs mostly absent, cottony hairs sparse to dense, glands absent or obscured to common;

primary lateral leaflets 3–6 per side, on distal 1/2–2/3(–3/4) of leaf axis, ± overlapping, largest ones cuneate-flabellate, 0.5–1.5(–2.5) × 0.4–2(–3) cm, distal 1/2 to whole margin unevenly incised 1/2 to completely to midvein (blade often medially split as well), ultimate teeth or segments 3–10, narrowly elliptic, 2–10(–15) × 1–3(–5) mm, apical tufts less than 1 mm, surfaces grayish green to white, not glaucous, straight hairs sparse to common (sparser adaxially), loosely appressed to ascending, 1–1.5 mm, soft, cottony hairs sparse to dense, glands sparse or obscured 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

1–3.

0–1.

Inflorescences

2–15(–25)-flowered, openly cymose.

1–5(–7)-flowered.

Pedicels

(1–)1.5–2.5(–4) cm, straight in fruit.

1–4 cm in flower, to 5 cm in fruit.

Flowers

epicalyx bractlets lanceolate to ovate, 2–5 × 1–1.5 mm;

hypanthium (3–)4–5 mm diam.;

sepals (3–)4–7 mm, apex acute;

petals 5–9(–10) × 4–8(–10) mm;

filaments (1–)2–4 mm, anthers (0.5–)1 mm;

carpels 15–25, styles 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

1.8 mm, smooth, not carunculate.

1.1–1.5 mm.

2n

= 72–73, 99, 100, 102.

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

Potentilla breweri

Potentilla nivea

Phenology Flowering summer. Flowering summer.
Habitat Rocky meadows, seasonally moist flats, rock crevices, often near streams and lakes Well-drained, exposed sites, ridge crests, coarse mineral soil, scree, usually on calcareous substrates
Elevation 1500–3600 m (4900–11800 ft) 400–3800 m (1300–12500 ft)
Distribution
from FNA
CA; NV; OR; WA
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[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

Of conservation concern.

Potentilla breweri differs from other members of sect. Multijugae in its often dense, cottony vestiture. Density of cottony hairs and leaflet dissection can differ significantly between first-formed and mid- to late-season leaves of P. breweri; in the description above, leaves are those predominant at anthesis.

Potentilla breweri is most common in the Sierra Nevada of California, with sporadic occurrences to the Cascade Range in southern Washington. Disjunct populations occur in the Ruby and Snake ranges in Nevada and on Steens Mountain in Oregon, where often introgressed with P. versicolor. Reports from Utah are based on collections of P. concinna var. proxima or possible hybrids between P. concinna var. proxima and P. ovina var. decurrens.

J. Clausen et al. (1940) concluded that Potentilla breweri (with P. versicolor as synonym) belonged with P. bruceae and P. drummondii as members of a cenospecies that probably also included unnamed species (possibly P. ovina var. decurrens) from the mountains of Colorado, Utah, and Wyoming. Chromosome number varied within populations, and high numbers of univalents were present.

Recognition of Potentilla breweri as a distinct species differs from recent treatments in which it was considered to be a variety or subspecies of P. drummondii, parallel to the treatment of P. bruceae. The present continental perspective of the genus, as well as additional fieldwork, has resulted in the return of all three to species rank (B. Ertter and D. Mansfield 2007). Placement of P. breweri in sect. Multijugae, separate from P. bruceae and P. drummondii in sect. Graciles, is based on the commonly prostrate habit, fully pinnate leaves, and deeply divided overlapping leaflets.

Although B. C. Johnston (1980) used Potentilla breweri var. viridis Jepson to accommodate greener-than-average sparsely cottony plants, including populations treated here as P. versicolor, the type is probably a sterile hybrid with P. wheeleri as one parent (B. Ertter 1992). The type of P. millefolia var. algida Jepson (included by Johnston in the synonymy of var. viridis) and comparable plants from north-central California combine features of P. breweri and P. versicolor but are more glandular than either. This variant, as well as exceptionally small plants from the Warner Mountains of California, may prove distinct.

(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. 170. 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. 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. 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. drummondii subsp. breweri, P. drummondii var. breweri, P. plattensis var. leucophylla P. prostrata subsp. floccosa
Name authority S. Watson: Proc. Amer. Acad. Arts 8: 555. (1873) Linnaeus: Sp. Pl. 1: 499. (1753)
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