Petrophytum cinerascens |
Petrophytum |
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Chelan rockmat, halfshrub rockmat |
rock-spiraea, rockmat, rockspirea |
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Habit | Shrubs, 1–5 dm diam. | Shrubs, cespitose, densely matted, 0.1–10 dm. | ||||||||
Stems | prostrate to decumbent, 2–8 cm, internodes (0.1–)1(–2) cm. |
1+, prostrate, decumbent, erect, or ascending; bark brown to dark brown, aging to gray; short and long shoots present; short shoots glabrous. |
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Leaves | blade oblanceolate to obtuse, 1–2.5(–3) × 0.2–0.4(–0.5) cm, palmately 3-veined, venation sometimes visible through hairs, apex obtuse, abaxial surface minutely canescent to strigose or cinereous, adaxial sometimes glandular. |
persistent, marcescent, cauline (tightly clustered), alternate, simple; petiole absent; blade oblanceolate to narrowly obtrullate, 0.2–2.5(–3) cm, coriaceous, margins flat, entire, venation indistinct, masked by hairs, or palmately 1–3-veined, surfaces glabrate, strigose, canescent, pilose, or sericeous. |
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Panicles | sometimes branched, 2–8(–15) × 1–5 cm, canescent to puberulent; bracts linear to oblanceolate, 5–10 mm, pilose. |
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Inflorescences | terminal, 10–100-flowered, panicles narrow or widely branched, flowers aggregated, dense, compact, puberulent, canescent to sericeous; bracts present, sometimes absent; bracteoles present. |
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Pedicels | 0.5–2(–4) mm; bracteoles 1(–2), extending from middle to apex of sepals, rarely beyond. |
present. |
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Flowers | 2–4(–6) mm diam.; hypanthium 1 mm, canescent; sepals erect, ovate or lanceolate, 1–1.5 mm, margins ciliate, abaxial surface pubescent, glandular; petals oblanceolate or narrowly ovate, 1–2.5 mm, apex acute or rounded; stamens 20–25, lengths 1.3 times petals (1.3–1.5 times sepals); carpels (3–)5(–6), distinct. |
2–6 mm diam.; epicalyx bractlets 0; hypanthium hemispheric, turbinate, 0.5–1 mm, canescent, pilose, or sericeous, sometimes glandular; sepals 5, erect or reflexed, ovate to lanceolate; petals 5, persistent, withering, white, oval to oblong, obovate, or oblanceolate; stamens 20–40, equal to or longer than petals; torus thickened basally, margins crenulate or entire; carpels (3–)5(–6)[–7], abaxially or adaxially connate or free, hirsute to pilose adaxially, styles terminal, stigmas minute; ovules 2 or 3[or 4]. |
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Fruits | aggregated follicles, (3–)5(–6), lanceoloid, 1.5–2 mm, coriaceous, glabrous, glabrate, or sparsely pilose, dehiscent along abaxial and adaxial sutures; hypanthium persistent; sepals persistent, erect to reflexed; styles deciduous or persistent. |
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Seeds | 1 or 2, fusiform to terete. |
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Follicles | 2 mm. |
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x | = 9. |
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Petrophytum cinerascens |
Petrophytum |
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Phenology | Flowering Jun–Aug. | |||||||||
Habitat | Crevices and ledges of outcrops, gneiss, schist, or granite | |||||||||
Elevation | 200–600 m (700–2000 ft) | |||||||||
Distribution |
WA
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w United States; sc United States; ne Mexico |
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Discussion | Of conservation concern. Petrophytum cinerascens grows in crevices and ledges of outcrops above the Columbia River where there is little or no soil; it was found only on rocky outcrops of gneiss, schist, and granite between Chelan and Wenatchee in central Washington (D. J. Moore et al. 1998); C. L. Hitchcock et al. (1955–1969, vol. 3) erroneously cited its habitat as basaltic cliffs, which is the more common rock type on the Columbia River plateau. Moore et al. evaluated the ability of P. cinerascens for photosynthetic acclimation to increased growth temperature and drought stress under short-term experimental conditions, and concluded that it could not acclimate to such changes; they suggested that this endemic species might be at risk of extinction if warmer, drier local conditions result from projected climate changes. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species 3 (3 in the flora). Taxa of Petrophytum are widely distributed in the mountains of western United States and northeastern Mexico, with P. caespitosum subsp. caespitosum the most widely distributed. The three other taxa recognized in this treatment, P. caespitosum subsp. acuminatum, P. cinerascens, and P. hendersonii, are isolated endemics with small ranges. With a single widely distributed taxon and three local endemics, it seems probable that taxa with closer geographical proximity would be likely to have greater morphological similarity. When C. Sterling (1966) examined carpel morphology in P. caespitosum, P. cinerascens, P. elatius [= P. caespitosum subsp. caespitosum], and P. hendersonii, he found that P. elatius and P. hendersonii had similar distributions of character states in five anatomical characters, yet differed as to whether carpels were fused (P. hendersonii) by their ventral bundles or distinct (P. elatius); P. caespitosum and P. cinerascens differed in only one character: carpels ventrally fused in P. caespitosum and distinct in P. cinerascens. Such incongruence of character states is seen also in leaves, flowers, and seeds; it is complicated by the reduction of these plants. In molecular phylogenetic analyses of Rosaceae (D. Potter et al. 2007), Petrophytum was sister to Kelseya, with Spiraea basal to the pair. In a more detailed study of Spiraeeae (Potter el al. 2007b), Kelseya was sister to Petrophytum and Spiraea; however, the three topologies were not well supported and additional work may show Kelseya and Petrophytum to be sister taxa. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 9, p. 412. | FNA vol. 9, p. 411. | ||||||||
Parent taxa | Rosaceae > subfam. Amygdaloideae > tribe Spiraeeae > Petrophytum | Rosaceae > subfam. Amygdaloideae > tribe Spiraeeae | ||||||||
Sibling taxa | ||||||||||
Subordinate taxa | ||||||||||
Synonyms | Spiraea cinerascens, Luetkea cinerascens | Spiraea unranked P. | ||||||||
Name authority | (Piper) Rydberg: in N. L. Britton et al., N. Amer. Fl. 22: 253. (1908) | (Nuttall ex Torrey & A. Gray) Rydberg: Mem. New York Bot. Gard. 1: 206. (1900) | ||||||||
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