Heuchera grossulariifolia |
Heuchera cylindrica |
|
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gooseberry-leaf alumroot |
alpine alumroot, lava alumroot, poker alum-root, round-leaf alumroot |
|
Habit | Herbs acaulescent; caudex branched. | Herbs acaulecent; caudex branched. |
Flowering stems | 15–65 cm, glabrous or short stipitate-glandular. |
10–90 cm, short or long stipitate-glandular. |
Leaves | petiole glabrous or short stipitate-glandular; blade cordate or orbiculate, shallowly 3–5-lobed, 1–7 cm, base cordate, lobes rounded, margins dentate, apex obtuse, surfaces glabrous or short stipitate-glandular. |
petiole glabrous or short to long stipitate-glandular; blade ovate to orbiculate, deeply 5–7-lobed, 2.2–8 cm, base cordate, truncate, or cuneate, lobes rounded, margins dentate, apex acute to obtuse, surfaces glabrous or short or long stipitate-glandular. |
Inflorescences | dense, interrupted. |
dense; (bracts subtending pedicels sometimes strongly fringed). |
Flowers | hypanthium weakly bilaterally symmetric, free 1.2–1.9 mm, cream, broadly campanulate, 4–7 mm, short stipitate-glandular; sepals erect, often red-tipped, equal, 2 mm, apex rounded; petals erect, pink or white, spatulate to narrowly oblanceolate, (clawed), unlobed, 1–3 mm, margins entire; stamens included 1.5 mm; (filaments strongly incurved, shorter than and almost concealed by anthers); styles included to 1 mm, 0.5 mm, 0.1+ mm diam. |
hypanthium weakly bilaterally symmetric, free 1–2 mm, cream or yellow, often tinged red or green, especially at base, broadly campanulate, 6–8.5 mm, short stipitate-glandular and sometimes long stipitate-glandular; sepals erect, sometimes red-tinged, equal, 2.5–5 mm, apex rounded or obtuse; petals absent or 1–5, erect, green, narrowly oblanceolate, unlobed, 1 mm, margins entire; stamens included 1–2 mm; (filaments erect, straight, stout, to 2 times length of anthers); styles included 2–3 mm, 0.5–1 mm, 0.1+ mm diam. |
Capsules | ovoid, 5 mm, beaks divergent, not papillose. |
ovoid, 6–10 mm, beaks divergent, not papillose. |
Seeds | dark brown, ellipsoid, 0.6 mm. |
dark brown, oblong-ellipsoid, 0.6–0.9 mm. |
2n | = 14, 28. |
= 14, 28. |
Heuchera grossulariifolia |
Heuchera cylindrica |
|
Phenology | Flowering May–Aug. | Flowering Apr–Aug. |
Habitat | Grassy hillsides, rocky canyon walls, alpine talus slopes | Rocky soil, cliffs, to subalpine and alpine talus slopes |
Elevation | 100-3400 m (300-11200 ft) | 1000-3400 m (3300-11200 ft) |
Distribution |
ID; MT; NV; OR; WA
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CA; ID; MT; NM; NV; OR; WA; WY; AB; BC
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Discussion | Heuchera grossulariifolia includes both diploids and autotetraploids. K. A. Segraves and J. N. Thompson (1999) analyzed floral traits and flowering phenology in diploid and autotetraploid plants. Overall, plant size was greater in tetraploids than in diploids; flowers of tetraploids were larger (average hypanthium 6.5 mm) than those of diploids (average hypanthium 5.5 mm) and had a slightly different shape and phenology, but the diploids and tetraploids were not assigned taxonomic status in their study. Diploids and tetraploids were mixed in some populations, where characters intergraded (D. E. Soltis, pers. comm.). The autotetraploids have had two to seven independent origins from diploid progenitors, and do not represent a monophyletic lineage (Segraves and Thompson; Segraves et al. 1999). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Some features of Heuchera cylindrica show great variation, including the type and amount of indument on the leaves, petioles, and stems, lobation and shape of leaf base, difference in flower size, complicated by rapid growth of the hypanthium during and after anthesis, change in filament-to-anther ratio before and after anthesis, relative degree of development of bracts of flowering stems, degree of disc development, and relative length and degree of divergence of the beaklike styles of the fruit. We agree with P. K. Holmgren and N. H. Holmgren (1997) that there is no value in recognizing infraspecific taxa in H. cylindrica until a more thorough phylogenetic study can show some correlation between morphological variation and infraspecific categories. A new species, Heuchera woodsiaphila P. Alexander, from between 2550 and 2900 meters elevation in the Capitan Mountains of Lincoln County, New Mexico, was published just as this treatment was going to press, and there was not adequate time to evaluate it or add it here. Alexander considered it closest to H. cylindrica, but pointed out that its proper status is difficult to determine and that it might be better treated as a variety of H. cylindrica. The Blackfoot Indians used decoctions of roots of Heuchera cylindrica for diarrhea and as an astringent. The Flathead infused or chewed roots for diarrhea and stomach cramps. The Kutenai used decoctions of roots for “aching bones” and tuberculosis. The Okanagan-Colville used decoctions of roots as a tonic for the “changing of the blood” and, especially for children and babies, to rinse out the mouth for sore throats. They applied a poultice of mashed, peeled roots to sores and cuts, and mixed roots with puffball spores as a salve for diaper rash. The Shuswap Indians took decoctions of leaves and roots for diarrhea. The Thompson Indians applied chewed leaves and roots on sores or wounds and drank an infusion of roots for liver trouble (D. E. Moerman 1998). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 8, p. 103. | FNA vol. 8, p. 101. |
Parent taxa | ||
Sibling taxa | ||
Synonyms | H. cusickii, H. grossulariifolia var. tenuifolia, H. tenuifolia | H. cylindrica var. alpina, H. cylindrica var. glabella, H. cylindrica var. orbicularis, H. glabella, H. ovalifolia, H. woodsiaphila |
Name authority | Rydberg: Mem. New York Bot. Gard. 1: 196. (1900) | Douglas: in W. J. Hooker, Fl. Bor.-Amer. 1: 236. (1832) |
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