Horkelia cuneata var. sericea |
Horkelia |
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coast horkelia, Kellogg's horkelia, wedgeleaf horkelia |
horkelia |
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Habit | Plants grayish-sericeous; eglandular hairs dense, ascending to appressed, glandular hairs obscured. | Herbs, perennial, rosetted, tufted, or matted, often resinously aromatic, 0.3–10(–12) dm, sparsely to densely hairy, inconspicuously to conspicuously glandular; compactly to ± loosely rhizomatous. | ||||||||||||||||||||
Stems | decumbent to ascending, 2–5(–7.5) dm. |
1–10+, decumbent to erect, rarely prostrate, green, reddish, or stramineous. |
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Leaves | marcescent or winter-persistent, primarily basal, cauline 1–6(–10), gradually or abruptly reduced distally, alternate, odd-pinnate; stipules persistent, basally adnate to petiole, linear to lanceolate or elliptic, margins entire or pinnately divided into linear to filiform segments; petiole present; blade oblanceolate-oblong to linear in outline, planar to cylindric, (1–)2–30(–40) cm, foliaceous, leaflets (3–)5–41, separate or congested and overlapping, terminal usually ± confluent with distalmost lateral ones, elliptic-oblong to ovate or flabellate in outline, margins flat, shallowly toothed to deeply divided into oblanceolate lobes, sometimes nearly entire except for 3-toothed apex, rarely completely entire, venation palmate to pinnate. |
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Leaflets | 5–10 per side, obovate, (5–)10–25(–30) mm, not distinctly pinnately veined. |
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Inflorescences | usually ± congested; most flowers arranged in glomerules. |
terminal, 3–200-flowered, open to congested cymes, flowers arranged individually, in corymbiform clusters, and/or in ± globose glomerules, these sometimes capitate; bracts present at proximal nodes, ± leafy, becoming reduced distally; bracteoles absent. |
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Pedicels | 1–3 mm, proximalmost to 12 mm. |
present, usually straight in fruit, sometimes reflexed or recurved. |
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Flowers | hypanthium interior rim densely pilose; petals oblanceolate, 1.5–3 mm wide; filaments 1–3 × 0.5–1 mm. |
4–17 mm diam.; epicalyx bractlets 5; hypanthium ± cupulate with flattened bases, 1–5.5 mm, less than 1/2 to nearly as deep as wide, interior often with band of hairs; sepals 5, spreading to strongly reflexed, usually lanceolate, sometimes ovate to triangular; petals 5, usually white, sometimes pink- to rose-veined or cream, usually narrowly oblanceolate-elliptic to obovate, sometimes linear to round, usually equal to or longer than sepals; stamens 10, shorter than petals, filaments usually ± erect, ± flattened, forming tube, anther thecae dehiscing introrsely; torus conic; carpels 2–200(–220), glabrous, styles subterminal; ovule 1. |
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Fruits | aggregated achenes, (1–)2–200(–220), obliquely ovoid to reniform, 0.8–3 mm, glabrous; hypanthium persistent; sepals persistent, erect; styles tardily deciduous, jointed, usually ± rough-thickened basally, otherwise mostly filiform. |
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x | = 7. |
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2n | = 28. |
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Horkelia cuneata var. sericea |
Horkelia |
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Phenology | Flowering summer. | |||||||||||||||||||||
Habitat | Coastal stabilized dunes and hills, coastal scrub communities | |||||||||||||||||||||
Elevation | 0–200 m (0–700 ft) | |||||||||||||||||||||
Distribution |
CA |
w North America; nw Mexico |
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Discussion | Of conservation concern. Historic populations of var. sericea occurred along the immediate coast from Alameda and Marin counties south at least to Santa Barbara County, with some littoral collections of Horkelia cuneata from Los Angeles and San Diego counties having some sericea characteristics. Reports from farther north are all based on misidentifications, for example, of H. californica in Sonoma County. The most distinctive specimens are from the northern populations in Alameda, Marin, San Francisco, and San Mateo counties, all of which apparently no longer exist. Of the recently confirmed extant populations, those that come closest to justifying continued recognition of var. sericea are in Monterey, San Luis Obispo, and Santa Cruz counties. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species 20 (20 in the flora). As discussed under 9. Ivesia, recognition of the ivesioid genera including Horkelia results in a paraphyletic Potentilla, which the first author does not find sufficient to dictate generic circumscriptions. On the basis of morphology and biogeography, Horkelia itself is likely nested within Ivesia as the branch that has radiated primarily within the California Floristic Province (see discussions under Ivesia regarding discordance with M. Töpel et al. 2012, http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0050358). Ivesia in the strict sense consists of an exceptionally diverse array of well-defined species; in contrast, Horkelia is more morphologically coherent as a genus but with species less sharply defined. The primary unifying features of the genus result from a flower specifically adapted for bee pollination: a relatively deep, flat-bottomed hypanthium containing abundant nectar, to which access is restricted by the columnar arrangement of ten erect stamens with flattened filaments, at least in early flowering. Anthers open introrsely by adaxial slits so that pollen is deposited on a visitor forcing its way into the staminal column. Other diagnostic characteristics of Horkelia include a distinctive resinous aroma in most species (except sect. Tridentatae and sect. Hispidulae) and various levels of glandularity. The terminal leaflet is most often lobed and/or confluent with lateral leaflets, in contrast to Drymocallis, which is often confused with Horkelia. Leaves range from planar with distinct leaflets to cylindric with overlapping leaflets, the latter condition often a response to drought stress in species that are normally planar-leaved. Sepals are often strongly reflexed. Stem lengths given below include inflorescences. Leaflet descriptions are based primarily on mid rachis leaflets of the larger basal leaves present at flowering; leaflets on the smaller outermost leaves formed early in the growing season are often less divided and less hairy. Counts of leaflet marginal segments include both shallow (teeth) and deep (lobes) ultimate divisions. Flowers are often aggregated into a single corymbiform cluster or one to many more globular glomerules, some of which are tightly capitate. Hypanthia interiors are glabrous in most species, except for the hairs surrounding the torus; some taxa are also more or less pilose on the internal hypanthial walls, especially just below the rim. Sepals are described as spreading or reflexed based on their orientation at anthesis. Larger and smaller anthers often are alternating; measurements are primarily of the larger filaments, with width measured at the base. See under 8. Potentilla and 9. Ivesia for additional discussion of special terminology. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 9, p. 255. | FNA vol. 9, p. 246. | ||||||||||||||||||||
Parent taxa | ||||||||||||||||||||||
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Synonyms | H. californica var. sericea, H. cuneata subsp. sericea, H. kelloggii, H. sericea, Potentilla kelloggii, P. lindleyi var. sericea | Potentilla section H., Potentilla subg. H. | ||||||||||||||||||||
Name authority | (A. Gray) Ertter & Reveal: Novon 17: 319. (2007) | Chamisso & Schlechtendal: Linnaea 2: 26. (1827) | ||||||||||||||||||||
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