Potentilla subjuga
Potentilla pedersenii
Colorado cinquefoil
not sheathed with marcescent whole leaves.
(0.8–)1–2.5(–3.5) dm.
ascending to nearly erect, 0.4–2 dm.
usually palmate with additional lateral leaflets, sometimes pinnate, 3–10(–14) cm;
petiole 1.5–5 cm, vestiture seasonally dimorphic, long hairs abundant, spreading on first-formed leaves, tightly appressed to ascending on later-formed leaves, 1–2 mm, ± stiff (especially on later-formed leaves), cottony and crisped hairs usually absent, glands absent or sparse;
leaflets (3–)5 at tip of leaf axis plus 1(–2) additional pair(s) separated from tip by 3–20 mm, on distal 1/10–1/3(–1/2) of leaf axis, largest leaflets oblanceolate-oblong, (0.5–)1.5–2.5(–3) × 0.3–1 cm, ± whole margin incised 1/2–2/3(–3/4) to midvein, teeth (2–)4–9 per side, usually touching to strongly overlapping, sometimes separate, 2–6 mm, surfaces usually strongly dissimilar (less so on first-formed leaves), abaxial usually white, straight hairs ± abundant (mostly on veins), 1–2 mm, cottony or crisped/cottony hairs ± dense (sparser on first-formed leaves), glands absent or obscured, adaxial green (to grayish), straight hairs sparse to common, 0.5–1.5 mm, cottony and crisped hairs absent, glands sparse.
often both ternate and palmate or subpalmate on same plant, 2.5–4 cm;
petiole 1.5–2.5 cm, long hairs common to abundant, loosely appressed to ascending-spreading, 1–2 mm, weak to ± stiff, verrucose, crisped(/short) hairs absent or sparse to common, cottony hairs absent, glands sparse to common;
leaflets 3–5, proximalmost separated by 0–2 mm, central broadly elliptic to obovate, 1–1.5 × 0.5–0.9 cm, petiolules 1–2 mm, distal 2/3–3/4 of margin incised 1/2–3/4 to midvein, teeth (2–)3–4 per side, 4–6 mm, apical tufts ± 1 mm, abaxial surfaces grayish white to white, long hairs abundant (sometimes obscuring entire surface), cottony-crisped hairs abundant to dense, short hairs absent or obscured, glands sparse to common but usually obscured, adaxial grayish green to gray, long hairs sparse to abundant, 1–1.5(–2) mm, ± weak, short (short-crisped) hairs absent or sparse, rarely common, cottony hairs absent, glands absent or sparse, rarely common.
1–3.
0–2.
3–20(–30)-flowered.
(1–)3–7-flowered, open, branch angle 30–50°.
0.5–2 cm (proximal to 3 cm).
1–2 cm, proximal to 4 cm.
epicalyx bractlets narrowly to broadly lanceolate, 2–5(–6) × 1–1.5 mm;
sepals 4–7 mm, apex acute to acuminate;
petals 4–8 × 4–8 mm;
filaments (0.5–)1–2 mm, anthers 0.3–0.8 mm;
carpels 15–30, styles filiform to filiform-tapered, ± papillate-swollen in less than proximal 1/5, 1.5–2 mm.
epicalyx bractlets narrowly ovate to elliptic, 4–5 × 1–1.4 mm;
hypanthium 3–4 mm diam.;
sepals 4–6 mm, apex subacute to acute, glands sparse to common, usually not obscured;
petals pale yellow, usually not overlapping, 6–7 × 4–8 mm, distinctly longer than sepals;
filaments 1–2 mm, anthers ± 0.4 mm;
carpels 40–80, styles 0.8–0.9 mm.
1.2–1.6 mm.
1.1–1.2 mm.
Potentilla subjuga
Potentilla pedersenii
Potentilla subjuga is centered in the high mountains of Colorado and barely enters New Mexico in the Sangre de Cristo Mountains. Collections from Alberta also apparently belong to this species, but all known collections from Wyoming have been identified as different taxa, at least one currently undescribed. At its most distinctive, P. subjuga is easily recognized by its unique leaf division, with five palmate leaflets subtended by an additional pair (or two) of lateral leaflets. Southern populations, however, are more likely to have only three apical leaflets. The leaflets tend to be strongly bicolored with overlapping teeth, in contrast to most sympatric pinnate species. Petiole vestiture is also distinctive in being seasonally dimorphic, with long hairs on first-formed leaves spreading to ascending and those on later formed leaves tightly appressed, as well as more conspicuously verrucose. Unresolved infraspecific variation exists, and field observations suggest that P. subjuga readily hybridizes with sympatric species, creating a swarm of intermediate specimens.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
Potentilla pedersenii and P. uschakovii account for the majority of arctic populations previously included in a broadly defined P. rubricaulis. The diagnostic morphological characters between the two species can be variable and overlapping; they are treated separately in part because of differences in presumed parental combinations. Whereas P. pulchella is the probable sect. Pensylvanicae parent for both species, the putative sect. Niveae parent for P. pedersenii is P. arenosa subsp. arenosa; that of P. uschakovii is P. subvahliana. Reflecting this parentage, P. pedersenii is distinguished by caudex branches with no marcescent whole leaves, verrucose long hairs on petioles, and inflorescences with usually several relatively small flowers. In contrast, P. uschakovii often has marcescent whole leaves sheathing the caudex branches, smooth long hairs on petioles, and one- or few-flowered inflorescences with mostly larger flowers. These generalities aside, there is much variation within both species, such that each island or population group may have its own features; it is probable that both P. pedersenii and P. uschakovii have evolved from multiple hybridization events.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
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