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old man's beard, old-man's whiskers, prairie smoke, three-flower avens, three-sisters, torchflower

queen Charlotte avens

Habit Plants subscapose. Plants subscapose.
Stems

10–45 cm, downy to pilose, hairs 0.1–3 mm, sometimes septate-glandular.

13–30 cm, puberulent, hairs scattered, 0.1–1 mm.

Leaves

basal 4–30 cm, blade interruptedly pinnate, major leaflets 10–18, alternating with 6–16 minor ones gradually increasing in size distally, terminal leaflet slightly larger than major laterals;

cauline 1–5 cm, stipules adnate to leaf, indistinguishable from leaflets/lobes, blade bractlike, not resembling basal, opposite, pinnate-pinnatifid.

basal 5–25 cm, blade interruptedly lyrate-pinnate, major leaflets 5–7, interspersed with 2–8 minor ones increasing in size distally, terminal leaflet larger than major laterals;

cauline 1.5–4.5 cm, stipules adnate to leaf, indistinguishable from pair of lobes, blade bractlike, not resembling basal, simple, 3-fid.

Inflorescences

(1–)3–5(–7)-flowered.

1-flowered.

Pedicels

densely woolly, sometimes glandular.

densely puberulent, sometimes glandular.

Flowers

nodding, erect in fruit;

epicalyx bractlets 6–15 mm;

hypanthium maroon, purple, or greenish mottled with purple, may turn pale brown in fruit;

sepals erect, 7–14 mm;

petals erect, cream to yellowish suffused with pink or purple, or purple-veined, elliptic, 7–13 mm, shorter to longer than sepals, apex rounded to obtuse.

erect;

epicalyx bractlets 4–8 mm;

hypanthium green;

sepals erect to erect-spreading, 7–12 mm;

petals spreading, yellow, broadly obovate to nearly orbiculate, 14–16 mm, distinctly longer than sepals, apex broadly rounded to irregularly emarginate.

Fruiting tori

sessile, densely puberulent.

sessile, glabrous.

Fruiting styles

wholly persistent or distal 3–7 mm tardily deciduous, not or inconspicuously geniculate-jointed, 15–70 mm, apex not or occasionally ± hooked, pilose to apex or nearly so.

wholly persistent, not geniculate-jointed, 7–10 mm, apex not or ± hooked, pilose only on bases.

2n

= 112.

Geum triflorum

Geum schofieldii

Phenology Flowering summer.
Habitat Rocky runnels, cliffs, rock outcrops
Elevation 500–1000 m [1600–3300 ft]
Distribution
from FNA
AZ; CA; CO; IA; ID; IL; MI; MN; MT; ND; NM; NV; NY; OR; SD; UT; WA; WI; WY; AB; BC; MB; NT; ON; SK; YT; Mexico
[WildflowerSearch map]
[BONAP county map]
from FNA
BC
Discussion

Varieties 2 (2 in the flora).

At the beginning of the twentieth century, E. L. Greene described over a dozen species belonging to the Geum triflorum complex based on differences in leaf form and indument, the relative length and shape of the epicalyx bractlets and sepals, and petal length and shape. Most of these species were quickly reduced to synonymy by other botanists. When specimens are examined from across the continent, most of the characters used to separate species in the G. triflorum complex show nearly continuous variation. It seems best to treat these variants as belonging to one species. Whether and how to classify the variation within the species will remain controversial. Some character expressions correlate reasonably well with dividing the species into two varieties, as was first proposed by N. C. Fassett (1928). Variety triflorum occurs east of the Rocky Mountains and is typical of the grasslands covering the northern Great Plains; it also is the variety found in the mountains of Arizona and New Mexico. Variety ciliatum is common throughout the rest of the Rocky Mountains, the Sierra Nevada, and Cascade Range. Intermediate specimens occur here and there, particularly in Alberta and British Columbia.

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

Of conservation concern.

Geum schofieldii is one of the more attractive yet seldom seen species of avens in North America; it is known from the rocky wet mountains of the Queen Charlotte Islands and northern Vancouver Island.

Because Geum schofieldii appears to be intermediate morphologically between G. calthifolium and G. rossii, some botanists have considered it to be a hybrid and included it in synonymy with G. ×macranthum [G. calthifolium × G. rossii]. The 16-ploid chromosome number (2n = 112) of G. schofieldii suggests an allopolyploid origin. Geum rossii is not known to occur in the Queen Charlotte Islands or on Vancouver Island; the plants cannot be of recent hybrid origin. Geum ×macranthum is found in the Aleutian Islands and the Alaska Peninsula where the two parental species overlap. Compared to G. schofieldii, its leaves are more pinnate than lyrate-pinnate, with 9 to 13 major leaflets instead of 5 to 7. Also, G. ×macranthum appears to be sterile; G. schofieldii appears to be fertile, suggesting that the latter is a valid species. The distinctness of G. schofieldii pollen also supports its specific status (R. J. Hebda and C. C. Chinnappa 1990).

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

Key
1. Basal leaves with larger leaflets toothed or cleft less than 1/2 their lengths; fruiting styles persistent, 28–70 mm.
var. triflorum
1. Basal leaves with larger leaflets cleft more than 1/2 their lengths; fruiting styles: proximal segments persistent, 15–40 mm, distal segments tardily deciduous, 3–7 mm.
var. ciliatum
Source FNA vol. 9, p. 62. Treatment author: Joseph R. Rohrer. FNA vol. 9, p. 63. Treatment author: Joseph R. Rohrer.
Parent taxa Rosaceae > subfam. Rosoideae > tribe Colurieae > Geum Rosaceae > subfam. Rosoideae > tribe Colurieae > Geum
Sibling taxa
G. aleppicum, G. calthifolium, G. canadense, G. geniculatum, G. glaciale, G. laciniatum, G. macrophyllum, G. peckii, G. radiatum, G. rivale, G. rossii, G. schofieldii, G. urbanum, G. vernum, G. virginianum
G. aleppicum, G. calthifolium, G. canadense, G. geniculatum, G. glaciale, G. laciniatum, G. macrophyllum, G. peckii, G. radiatum, G. rivale, G. rossii, G. triflorum, G. urbanum, G. vernum, G. virginianum
Subordinate taxa
G. triflorum var. ciliatum, G. triflorum var. triflorum
Synonyms Erythrocoma triflora, Sieversia triflora
Name authority Pursh: Fl. Amer. Sept. 2: 736. (1813) Calder & Roy L. Taylor: Canad. J. Bot. 43: 1394. (1965)
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