The green links below add additional plants to the comparison table. Blue links lead to other Web sites.
enable glossary links

Brewer's cinquefoil

Alaska cinquefoil, finely villous cinquefoil

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

stout, sometimes ± 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, 0.2–1.5(–2) dm, lengths 1.5–3(–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.

1–5.5(–7) cm;

petiole 0.5–3.5(–5) cm, long hairs common to dense, ascending to spreading, loosely appressed, sometimes retrorse, 1–2(–3) mm, soft, smooth, crisped/short-cottony hairs usually sparse, sometimes common, glands absent or sparse to common or obscured;

leaflets overlapping, central broadly obovate to obtriangular, 0.8–2.5 × 0.6–2 cm, sessile to subsessile, base broadly cuneate, margins revolute, distal 1/2–2/3(–3/4) incised ± 1/2 to midvein, teeth 2–3(–4) per side, ± approximate to ± distant, surfaces ± dissimilar, abaxial grayish to white or yellowish white, long hairs 1.5–2.5 mm, cottony-crisped hairs ± dense, adaxial grayish green, long hairs abundant to dense, crisped hairs absent, sparse, or obscured.

Cauline leaves

1–3.

(0–)1–2(–3).

Inflorescences

2–15(–25)-flowered, openly cymose.

(1–)2–3(–4)-flowered.

Pedicels

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

0.5–3(–5) cm in flower, to 4(–6) 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 broadly lanceolate to narrowly ovate, 3–7(–8) × 1.5–3(–3.5) mm, 2/3 to as wide as sepals, margins ± revolute, red glands absent;

hypanthium (3–)4–6 mm diam.;

sepals 4–7(–8) mm, apex acute or rarely acuminate;

petals 5–10 × 6–12 mm, significantly longer than sepals;

filaments 1.1–1.4 mm, anthers 0.5–0.8 mm;

carpels 40–70, apical hairs absent or sparse (straight), styles narrowly columnar to conic-tapered, papillate-swollen in proximal 1/5 or less, 1–1.2 mm.

Achenes

1.8 mm, smooth, not carunculate.

0.9–2 mm.

2n

= 72–73, 99, 100, 102.

= 28 (Russian Far East).

Potentilla breweri

Potentilla villosula

Phenology Flowering summer. Flowering late spring to summer.
Habitat Rocky meadows, seasonally moist flats, rock crevices, often near streams and lakes Rocky alpine heaths, outcrops, scree and talus, gravel outwash plains, dry tundra, coastal bluffs, stabilized sand dunes, mostly on acidic bedrock
Elevation 1500–3600 m (4900–11800 ft) 0–2900 m (0–9500 ft)
Distribution
from FNA
CA; NV; OR; WA
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; AB; BC; YT; e Asia (Russian Far East)
[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 villosula was included previously in P. villosa; the two overlap in the southern and western Alaskan coasts, where a transition is suspected to be associated with differing ploidy levels. The plants from this area with silky hairs and multiflowered inflorescences are assigned to P. villosa; P. villosula has thicker, stiffer, and less silky hairs, fewer teeth per leaflet, narrower bracts, fewer and smaller flowers with narrower epicalyx bractlets and sepals, and fewer achenes (sometimes with single apical hairs). While P. villosa is restricted to relatively rocky sites near the coast from western Alaska to Oregon, P. villosula often occurs on coastal sand dunes, farther inland, and/or farther to the north.

As circumscribed, Potentilla villosula is a major plant of Alaska, especially of the Bering Sea region. The species extends from Alaska and the Yukon to at least central British Columbia. Most of the range given by E. Hultén (1968) for P. villosa belongs to P. villosula. W. J. Cody (1996) accepted the name P. villosula for a common south-central Yukon plant, but the majority of the plants mapped by Cody probably belong to P. subgorodkovii (although the distinction between the two species needs more resolution). Provisionally included here are plants from southern and central Yukon south through the Canadian Rockies, possibly including the type of P. nivea subsp. fallax A. E. Porsild. Such plants tend to be significantly smaller overall than Alaskan P. villosula; at least some have straight hairs on carpel apices.

J. Soják (2004) believed that Potentilla villosula evolved from crosses between P. villosa and P. vulcanicola. The affinity with P. villosa is seen in the sericeous vestiture, number of leaflet teeth, and flower number and size, and with P. vulcanicola in the frequent occurrence of straight hairs on carpel apices in both species. Plants with columnar caudex branches, representing a significant part of the Alaskan material, have been called subsp. congesta. This morphology results from the persistence of marcescent whole leaves for several years (in typical P. villosula only sheaths and petioles are retained). This character suggests that P. subvahliana, with which the form called subsp. congesta is sympatric, may be part of its parentage. Potentilla villosula is accepted here in a fairly collective sense, possibly including several hybrid lineages, but with P. villosa a part of them all.

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

Source FNA vol. 9, p. 170. FNA vol. 9, p. 202.
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. tikhomirovii, P. townsendii, P. uliginosa, P. uschakovii, P. vahliana, P. verna, P. versicolor, P. villosa, P. vulcanicola, P. wheeleri
Synonyms P. drummondii subsp. breweri, P. drummondii var. breweri, P. plattensis var. leucophylla P. villosula subsp. congesta
Name authority S. Watson: Proc. Amer. Acad. Arts 8: 555. (1873) Jurtzev: in A. I. Tolmatchew, Fl. Arct. URSS 9(1): 319. (1984)
Web links