Petrophytum caespitosum |
Petrophytum |
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mat rock-spirea, rockmat spirea, rockrose, Rocky Mountain rockmat |
rock-spiraea, rockmat, rockspirea |
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Habit | Shrubs, 1–10+ dm diam. | Shrubs, cespitose, densely matted, 0.1–10 dm. | ||||||||||||
Stems | prostrate or decumbent, loosely intertwined, 1–4+ cm, and erect or ascending, tightly coalesced, 0.2–0.5 cm, internodes 0.1–1 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 spatulate, 0.4–1.8 × 0.2–0.4 cm, venation rarely visible except on long-shoot leaves, 1(–3)-veined, apex acute, abaxial surface pilose to sericeous, rarely sparsely strigose on lamina and veins. |
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 | widely branched to compact and racemose, [0.5–]1–15[–20] × 0.5–6 cm, sericeous; bracts subulate to narrowly obtrullate, 3–8 mm, pilose to sericeous. |
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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 | 0.5–2.5 mm; bracteoles 1, extending from middle to well beyond apex of sepals. |
present. |
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Flowers | 3–6 mm diam.; hypanthium 1 mm, densely sericeous; sepals erect, ovate-lanceolate, 1–1.5 mm, margins sericeous, abaxial surface sericeous to tomentose; petals narrowly oblanceolate, 1–2.5 mm, apex obtuse to slightly cleft or acute to acuminate; stamens 20, lengths 1.5–2(–2.5) times petals (1.5–3 times sepals); carpels (3–)5(–6), adaxially connate. |
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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2n | = 18. |
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Petrophytum caespitosum |
Petrophytum |
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Distribution |
AZ; CA; CO; ID; MT; NM; NV; SD; TX; UT; WA; ne Mexico
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w United States; sc United States; ne Mexico |
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Discussion | Subspecies 2 (2 in the flora). Petrophytum caespitosum primarily inhabits arid rocky outcrops and talus slopes at high elevations in mountain ranges of the western United States and northeastern Mexico. (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. 413. | FNA vol. 9, p. 411. | ||||||||||||
Parent taxa | Rosaceae > subfam. Amygdaloideae > tribe Spiraeeae > Petrophytum | Rosaceae > subfam. Amygdaloideae > tribe Spiraeeae | ||||||||||||
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Subordinate taxa | ||||||||||||||
Synonyms | Spiraea caespitosa, Eriogynia caespitosa, Luetkea caespitosa | Spiraea unranked P. | ||||||||||||
Name authority | (Nuttall) Rydberg: Mem. New York Bot. Gard. 1: 206. (1900) | (Nuttall ex Torrey & A. Gray) Rydberg: Mem. New York Bot. Gard. 1: 206. (1900) | ||||||||||||
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