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Brewer's cinquefoil

Sandhills cinquefoil

Habit Plants rosetted to ± matted; taproots not fleshy-thickened.
Stems

prostrate to ascending, (0.5–)1–3(–4.5) dm, lengths 2–4(–5) times basal leaves.

± erect, 2–4 dm.

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.

pinnate, 12–20(–30) cm;

petiole 5–10(–15) cm, long hairs ± abundant, spreading to ascending, 0.5–1 mm, weak to ± stiff, short hairs abundant to dense, cottony or crisped hairs absent, glands sparse to abundant, often obscured;

leaflets 4–6(–9) per side, on distal (1/3–)1/2–3/5 of leaf axis, slightly overlapping, terminal ones oblanceolate to narrowly elliptic, 3–6 × 0.8–1.2(–1.5) cm, margins strongly revolute, incised ± 1/2 to midvein, undivided medial blade 5–9 mm wide, teeth 8–12 per side, narrowly triangular to lanceolate, surfaces ± dissimilar, abaxial grayish, long hairs ± sparse (or not differentiated from short hairs), 0.5–1.5 mm, weak, short hairs abundant to dense, cottony or crisped hairs absent, glands sparse or obscured, adaxial ± green, straight hairs (long and short not differentiated) abundant, spreading to ascending, 0.2–0.5 mm, cottony and crisped hairs absent, glands sparse to abundant, often obscured.

Cauline leaves

1–3.

(1–)2–4.

Inflorescences

2–15(–25)-flowered, openly cymose.

10–40-flowered, congested or elongating in fruit.

Pedicels

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

± 0.1 cm (proximal to 1.2 cm).

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 ovate-acuminate, (3–)4–8(–10) × 2–3 mm, lengths 1–2 times sepals, margins ± revolute;

hypanthium (4–)5–10 mm diam.;

sepals 3–5 mm, apex acute to obtuse, abaxial surfaces: venation moderate, glands ± abundant, obscured to evident;

petals pale yellow, 3–5 × 2–4 mm, lengths ± equal to or shorter than sepals;

filaments 1–1.5 mm, anthers 0.5–0.8 mm;

carpels 80–90, styles papillate-swollen in proximal 3/4+, 1–1.2 mm.

Achenes

1.8 mm, smooth, not carunculate.

± 1 mm, ± rugose.

2n

= 72–73, 99, 100, 102.

= 14.

Potentilla breweri

Potentilla lasiodonta

Phenology Flowering summer. Flowering summer.
Habitat Rocky meadows, seasonally moist flats, rock crevices, often near streams and lakes Sandy sites in prairies
Elevation 1500–3600 m (4900–11800 ft) 300–1100 m (1000–3600 ft)
Distribution
from FNA
CA; NV; OR; WA
[WildflowerSearch map]
[BONAP county map]
from FNA
MN; ND; AB; MB; SK
[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 lasiodonta is a diploid relative of tetraploid P. pensylvanica, sharing similar velvety vestiture of dense short hairs, pinnate leaves, and epicalyx bractlets with revolute margins. The species differs in having larger epicalyx bractlets and less deeply incised leaflets. Plant height and leaf size are at the upper range of P. pensylvanica, and populations are evidently restricted to sandy substrates. Occurrence in Manitoba is based on B. L. Kohli and J. G. Packer (1976); no vouchers are in WIN. At least one collection from southeastern British Columbia (Brown 779, MO) approaches P. lasiodonta, but it is insufficient by itself to serve as a provincial record.

The fundamental ploidy and epicalyx distinctions of this species were established by B. L. Kohli and J. G. Packer (1976), who proposed the name Potentilla finitima. As noted by J. Soják (1994), the type of P. lasiodonta is the same entity. Potentilla atrovirens Rydberg and P. pensylvanica var. arida B. Boivin have sometimes been applied to this taxon; the types of both names fall within the circumscription of P. pensylvanica in the narrow sense (Packer, pers. comm.).

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

Source FNA vol. 9, p. 170. FNA vol. 9, p. 214.
Parent taxa Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Multijugae Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Pensylvanicae
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. 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
Synonyms P. drummondii subsp. breweri, P. drummondii var. breweri, P. plattensis var. leucophylla P. finitima
Name authority S. Watson: Proc. Amer. Acad. Arts 8: 555. (1873) Rydberg: in N. L. Britton et al., N. Amer. Fl. 22: 351. (1908)
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