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Newberry's cinquefoil

Norwegian cinquefoil, Norwegian or rough cinquefoil, potentille de norvège, rough cinquefoil

Stems

ascending to erect, (0.5–)2–5(–9) dm, hairs at base ± stiff, tubercle-based, glands absent or sparse, inconspicuous.

Leaves

ternate, rarely palmate, 3–15(–20) cm;

petiole 1–6(–10) cm, long hairs sparse to abundant, spreading to ascending, 1–2.5(–3) mm, usually ± stiff, ± crisped hairs absent or sparse to common, glands absent or sparse, inconspicuous;

leaflets 3(–5), at tip of leaf axis, separate to ± overlapping, largest ones broadly oblanceolate or elliptic to obovate, 1–6(–10) × 0.7–4(–5) cm, distal (1/2–)2/3–3/4+ of margin usually ± evenly incised 1/4–1/3 to midvein, teeth (3–)4–8(–15) per side, surfaces sparsely to moderately hairy, sometimes glabrate or abundantly hairy, glands mostly absent.

Basal leaves

petiole 1–3.5 cm, long hairs ± abundant, 0.5–1.5 mm, short hairs absent or sparse, rarely common;

leaflets 0.2–1 cm, lobes oblanceolate to narrowly elliptic, (0.5–)1–2 mm wide, longs hairs ± abundant, short hairs absent or sparse, glands sparse to abundant.

Inflorescences

5–40+-flowered.

Pedicels

(0.2–)0.5–2.5(–3) cm.

Flowers

epicalyx bractlets broadly lanceolate to elliptic, 1.5–4(–5) × (0.4–)0.8–1.3 mm;

sepals 2–4(–5) mm, apex ± acute;

petals (3–)4–6 × (2–)3–5 mm;

filaments 1–2(–2.5) mm, anthers 0.4–0.6 mm;

carpels 20–50.

epicalyx bractlets ± elliptic to narrowly ovate, (3–)4–8(–13) × 1.5–3(–5) mm;

hypanthium 4–7 mm diam.;

sepals 5–8 mm, apex acute to obtuse;

petals yellow, broadly obovate, (2–)3–5 × 2–4 mm;

stamens 15 or 20, filaments 0.7–2 mm, anthers 0.3–0.5 mm;

carpels 60–150, styles 0.7–0.8 mm.

Achenes

0.9–1.2 mm.

tan to brown, 0.8–1.3 mm, usually strongly rugose, without a corky protuberance.

2n

= 42, 56, 63, 70.

Potentilla newberryi

Potentilla norvegica

Phenology Flowering summer. Flowering summer.
Habitat Moist, sandy to clayey, more or less alkaline soil, especially where seasonally inundated near streams, ponds, and lakes Moist meadows, stream banks, lakeshores, roadsides, grasslands, hardwood and conifer woodlands, tundra
Elevation 1300–1800 m (4300–5900 ft) 300–2700 m (1000–8900 ft)
Distribution
from FNA
CA; NV; OR; WA
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; AL; AR; AZ; CA; CO; CT; DC; DE; GA; IA; ID; IL; IN; KS; KY; MA; MD; ME; MI; MN; MO; MT; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OK; OR; PA; RI; SC; SD; TN; TX; UT; VA; VT; WA; WI; WV; WY; AB; BC; MB; NB; NL; NS; NT; NU; ON; PE; QC; SK; YT; SPM; Mexico; Central America; Greenland; Eurasia [Introduced in South America, Pacific Islands (New Zealand)]
[WildflowerSearch map]
[BONAP county map]
Discussion

Potentilla newberryi grows in valley bottoms in south-central Oregon, northeastern California, and northwestern Nevada. The only specimen supposedly collected in south-central Washington (W. N. Suksdorf 2718, WTU) was gathered in 1898.

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

Potentilla norvegica is considered native in both North America and Eurasia, with the American race occasionally recognized as subsp. hirsuta for the stiff hairs on the stems, petioles, and pedicels of most plants in the flora area. This feature and other purported differences between the two races, in addition to being relatively subtle and inconstant, can be found in both America and Eurasia, though undoubtedly at least in part as introductions. Some populations in eastern Canada with glabrous stems have been distinguished as var. labradorica (for example, M. L. Fernald 1950), but such plants typically are intermixed with hairy individuals. The Löves (Á Löve 1954; Á Löve and D. Löve 1966) have argued that all three variants should be treated as distinct species due to chromosomal differences (hirsuta 2n = 56; labradorica 2n = 42; norvegica in the narrow sense 2n = 70) and obligate apomixis. Further research is needed to determine the taxonomic validity and rank of these expressions. If treated as species, P. flexuosa antedates P. labradorica (as noted by J. Soják 1969), while P. monspeliensis, although commonly used for the American race, is based on a European type (as summarized by A. Kurtto et al. in J. Jalas et al. 1972+, vol. 13).

An even greater challenge is determining native versus introduced ranges, especially given the likelihood that both native and Eurasian populations are widespread in North America. Achenes are produced prolifically and easily dispersed, to the extent that Potentilla norvegica is a contaminant in clover and hay fields and considered a weed at least in Canada (P. A. Werner and J. D. Soule 1976).

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

Source FNA vol. 9, p. 137. FNA vol. 9, p. 140.
Parent taxa Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Arenicolae Rosaceae > subfam. Rosoideae > tribe Potentilleae > Potentilla > sect. Rivales
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. millefolia, P. modesta, P. morefieldii, P. multijuga, P. multisecta, P. nana, 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. 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 Ivesia gracilis P. flexuosa, P. labradorica, P. monspeliensis, P. norvegica subsp. hirsuta, P. norvegica var. hirsuta, P. norvegica var. labradorica, P. norvegica subsp. monspeliensis
Name authority A. Gray: Proc. Amer. Acad. Arts 6: 532. (1865) — not P. gracilis Douglas ex Hooker 1830 Linnaeus: Sp. Pl. 1: 499. (1753)
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