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Brewer's cinquefoil

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

slender to 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, sometimes nearly erect, 0.5–1.5(–3) dm, lengths 2–4 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.

2–4 cm;

petiole 1–2.5 cm, long hairs common to abundant, spreading to ascending, rarely loosely appressed, 1–2 mm, ± stiff, verrucose, short-crisped hairs sparse to abundant, sometimes nearly absent, cottony hairs absent, glands sparse;

leaflets ± overlapping, central elliptic to obovate, 1–1.5 × 0.6–1.1 cm, petiolulate, base broadly cuneate, margins flat or slightly revolute, distal ± 2/3 incised ± 1/2 to midvein, teeth (3–)4 per side, ± approximate, surfaces ± dissimilar, abaxial reddish or greenish gray to white, long hairs 1 mm, cottony-crisped hairs common to dense, adaxial green or reddish to gray-green, long hairs sparse to abundant, short-crisped hairs absent or sparse to common.

Cauline leaves

1–3.

0–1.

Inflorescences

2–15(–25)-flowered, openly cymose.

2–5-flowered.

Pedicels

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

1–2 cm in flower, to 3(–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 elliptic to narrowly ovate, 4–6 × 1–2.5 mm, (1/2–)2/3 to as wide as sepals, margins revolute, sometimes flat, red glands usually common, conspicuous;

hypanthium 3.5–4.5 mm diam.;

sepals 5–7 mm, apex subacute;

petals 6–8 × (4–)5–8 mm, longer than sepals;

filaments 0.7–1.2 mm, anthers 0.4 mm;

carpels 40–60, apical hairs absent, styles columnar, strongly papillate-swollen in proximal 1/5–1/3, 0.9–1 mm.

Achenes

1.8 mm, smooth, not carunculate.

1.2–1.8 mm.

2n

= 72–73, 99, 100, 102.

= 42, 49 (Russian Far East).

Potentilla breweri

Potentilla tikhomirovii

Phenology Flowering summer. Flowering summer.
Habitat Rocky meadows, seasonally moist flats, rock crevices, often near streams and lakes Dry tundra meadows, loamy soil banks, sedge-herb slopes
Elevation 1500–3600 m (4900–11800 ft) 0–1100 m (0–3600 ft)
Distribution
from FNA
CA; NV; OR; WA
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; NT; NU; Greenland; Europe (Russia); Asia
[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.)

Potentilla tikhomirovii is an assumed hybrid species combining characteristics from P. arenosa subsp. arenosa of sect. Niveae (abaxial leaflet surfaces with crisped-cottony hairs, adaxial surfaces with both long and short hairs, petioles often with both long and short hairs, and flower shape and size) and P. hyparctica of sect. Aureae (crisped-cottony hairs often not fully covering abaxial leaf surfaces, reddish color in most plant parts, sepals and epicalyx bractlets relatively large, broad, less acute, and with many and reddish glands, which are often also on petioles and stipules).

Potentilla tikhomirovii has an interrupted range and is not very coherent morphologically. It forms large populations locally, probably by agamic seed propagation, and is a significant part of the Potentilla variation in northern and northeastern Greenland, Ellesmere Island, and parts of the Brooks Range, northern Alaska. Both the distributional and the morphologic patterns indicate that it has evolved multiple times in different regions, such that it is a borderline case for status as an independent species. Its large populations and significant distribution in some regions support recognition, as also does the paucity of obvious back-crosses with the parents.

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

Source FNA vol. 9, p. 170. FNA vol. 9, p. 201.
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. 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. 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
Name authority S. Watson: Proc. Amer. Acad. Arts 8: 555. (1873) Jurtzev: in A. I. Tolmatchew, Fl. Arct. URSS 9(1): 318. (1984)
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