Chrysosplenium |
Chrysosplenium wrightii |
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dorine, golden-carpet, golden-saxifrage, water-carpet |
Wright's golden carpet, Wright's golden-saxifrage |
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Habit | Herbs, rhizomatous, stoloniferous, (rhizomes and stolons with functional leaves or stolon leaves reduced, nonfunctional, scalelike); caudex absent. | |||||||||||||||||||||
Flowering stems | repent, decumbent, or ascending to erect, leafy or leafless, (1.2–)2–30 cm (often as short as 2 cm in C. wrightii), glabrous or sparsely to densely villous. |
erect, branching in distal 1/10–1/4(–1/3), (1.5–)2–11(–16) cm, sparsely to densely villous especially proximally, hairs reddish brown. |
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Leaves | cauline or arising from stolons or rhizomes, opposite or alternate; stipules absent; petiole present, glabrous or villous; blade ovate, depressed-ovate, depressed-elliptic, reniform, flabellate, or, sometimes, nearly orbiculate, unlobed, base attenuate, cuneate, truncate, or cordate, ultimate margins subentire, crenate, crenulate, or crenate-dentate, crenae sometimes prominent and margins appearing ± lobed, apex obtuse, rounded, or truncate, surfaces glabrous or sparsely villous to villous; venation palmate. |
alternate, fleshy. |
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Cauline leaves | absent or 1(–2); petiole 3–16(–24) mm, glabrous or sparsely villous, hairs reddish brown; blade ovate to broadly ovate, reniform, or flabellate, 3.5–12 × 4.5–19 mm, base cuneate, margins 3–7-crenate, usually glabrous, sometimes villous, hairs white, surfaces glabrous. |
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Inflorescences | simple or compound cymes, from terminal bud in rosette, 2–30-flowered, sometimes flowers solitary, bracteate. |
terminal, 3–30-flowered, compact cymes; bracts green or greenish yellow, usually purple-spotted, foliaceous, usually ovate to flabellate or, rarely, elliptic, 3–13 × 2–15 mm, margins subentire or 3–7-crenate. |
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Pedicels | absent or 0.1–1.5 mm. |
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Flowers | hypanthium 1/2–3/4 adnate medially or distally to ovary, 0.5–1.5 mm free from ovary, greenish or yellow-green; sepals 4, yellow, greenish yellow, green, greenish red, reddish orange, or purple, sometimes purple-spotted; petals absent; nectary disc conspicuous or apparently absent; stamens 2–8, usually 4 or 8; filaments lanceolate to narrowly oblong; ovary 1/2–3/4-inferior, 1-locular, carpels connate 3/4–4/5 their lengths; placentation parietal; styles 2; stigmas 2. |
hypanthium green or greenish yellow, sometimes purple-spotted distally, turbinate, 1.2–2.2 × 1.8–3.5 mm, glabrous; sepals spreading, greenish yellow, purple, or reddish orange, usually purple-spotted throughout or distally, rarely not spotted, broadly ovate to depressed-ovate or nearly round, 0.9–2.3 × 1.2–3.1 mm, apex obtuse to rounded; nectary disc prominent, yellow or purple, 8-lobed; stamens 8, 0.7–0.9 mm; anthers yellow or purple, 0.2–0.3 × 0.2–0.3 mm; styles 0.5–0.9 mm. |
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Capsules | (cuplike after dehiscence), 2-beaked (beaks divergent). |
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Seeds | dark brown or reddish brown, ellipsoid, ovoid, or spheroid, smooth. |
(2–)5–12, reddish brown, ovoid to ellipsoid, (0.8–)1–1.3 mm, glabrous. |
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Stolon(s) | leaves: petiole (7–)25–55(–68) mm, sparsely to densely villous, hairs reddish brown; blade depressed-ovate to reniform, 4–19 × 7–24 mm, base cordate or truncate, margins 5–9-crenate, usually purple-spotted, usually ciliate, hairs white, surfaces glabrous or sparsely villous, especially near petiole, hairs usually white, brown, or reddish brown, sometimes purple. |
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x | = 11. |
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2n | = 24. |
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Chrysosplenium |
Chrysosplenium wrightii |
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Phenology | Flowering Jun–Aug. | |||||||||||||||||||||
Habitat | Gravelly tundra and stream banks, boulder fields, scree slopes, solifluction terraces, seeps | |||||||||||||||||||||
Elevation | 0-2300 m (0-7500 ft) | |||||||||||||||||||||
Distribution |
North America; s South America; Eurasia |
AK; BC; YT; e Asia (Russia: Kamtchatka, e Siberia) |
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Discussion | Species ca. 60 (6 in the flora). A wide range of chromosome numbers has been reported in Chrysosplenium. M. Nakazawa et al. (1997) and D. E. Soltis et al. (2001b) hypothesized that these numbers arose from an ancestral base of x = 11, with multiple lines of dysploidy (reported as aneuploidy). The historical division of the genus into two major clades—opposite-leaved species and alternate-leaved species—is supported by flavonoid (B. A. Bohm and F. W. Collins 1979) and molecular data (Nakazawa et al.; Soltis et al.). Phylogenetic analyses using the rbcL and matK genes (Nakazawa et al.; Soltis et al.) have provided limited resolution for species-level relationships. The relationship of the alternate-leaved, North American species to those in Europe and Asia has not been examined in detail. Morphological similarities between the North American species and Eurasian Chrysosplenium alternifolium Linnaeus have caused some authors to treat C. iowense, C. rosendahlii, C. tetrandrum, and C. wrightii as infraspecific taxa of C. alternifolium. Each of them is maintained here as a distinct species pending further studies. Stamen number can vary among flowers within an inflorescence in some alternate-leaved species (C. O. Rosendahl 1947; J. G. Packer 1963), with lateral flowers sometimes smaller and having fewer stamens than the central flowers. In species usually producing eight stamens, Packer observed that variable stamen numbers resulted from the systematic failure of stamens to develop. Stamens alternating with the styles are suppressed first. In flowers with fewer than four stamens, the stamens alternating with the styles are suppressed. This corresponds with developmental observations made by L.-P. Ronse Decraene et al. (1998) in Chrysosplenium alternifolium Linnaeus. D. B. O. Savile (1953) demonstrated splash-cup dispersal of seeds in Chrysosplenium americanum, reporting a maximum dispersal distance of 40 cm in the laboratory. R. M. Weber (1979) reported a maximum dispersal distance of 30 cm for C. iowense in the field and 45 cm in the laboratory. Among three Japanese species examined in the field, H. Nakanishi (2002) reported a maximum dispersal distance of 116 cm. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
H. Hara (1957) recognized two varieties of Chrysosplenium wrightii. He considered var. wrightii to be restricted to Herald Island, the type locality, and var. beringianum (Rose) H. Hara to be the element in southern Alaska, St. Matthew Island and the Pribiloff Islands, and across the Aleutian Islands to Kamtchatka. He distinguished the varieties by the indumentum of the flowering stems and thickness of the leaf blades. These characters vary too widely among populations to warrant recognition of infraspecific taxa. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 8, p. 70. | FNA vol. 8, p. 75. | ||||||||||||||||||||
Parent taxa | ||||||||||||||||||||||
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Synonyms | C. alternifolium var. wrightii | |||||||||||||||||||||
Name authority | Linnaeus: Sp. Pl. 1: 398. (1753): Gen. Pl. ed. 5, 189. 1754 , | Franchet & Savatier: Enum. Pl. Jap. 2: 356. 1878 , | ||||||||||||||||||||
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