Aphanes |
Rosaceae subfam. rosoideae |
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parsley-piert, piert |
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Habit | Herbs, annual, prostrate to ascending, 0.1–3 dm, soft-hairy; taprooted. | Herbs, shrubs, or subshrubs. | ||||||||
Stems | 1–10+, erect, ascending, or spreading. |
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Leaves | not persistent, cauline, alternate, simple (deeply lobed); stipules persistent, free or distally adnate to petiole, asymmetric, ± orbicular to ovate, margins lobed; petiole present, short; blade cuneate, 0.2–1 cm, herbaceous, deeply divided into 2–3(–5) segments, each segment (1–)2–3(–6)-lobed, margins flat, entire, venation pinnate. |
alternate, rarely opposite, pinnately compound, sometimes simple or palmately compound; stipules present, rarely absent. |
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Inflorescences | lateral, 4–12-flowered, condensed cymes, often hidden by stipules; bracts absent; bracteoles absent. |
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Pedicels | present. |
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Flowers | 0.7–1.1 mm diam.; epicalyx bractlets (0–)4; hypanthium subglobose to ellipsoid or ovoid, 0.7–2 mm; sepals 4, connivent or erect to spreading, ovate to narrowly triangular; petals 0; stamens 1(or 2); torus absent or reduced; carpel 1, hairy, styles basal, stigmas capitate; ovule 1. |
torus usually enlarged, sometimes small or absent; carpels 1–260(–450), distinct, free, styles distinct, rarely connate (Roseae); ovules 1(or 2), collateral (Rubeae) or superposed (Fallugia, Filipendula). |
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Fruits | achenes, 1, narrowly ovoid, 0.8–2.5 mm; hypanthium persistent; sepals persistent, erect; styles deciduous. |
achenes or aggregated achenes sometimes with fleshy, urn-shaped hypanthium or enlarged torus, sometimes aggregated drupelets; styles persistent or deciduous, not elongate (elongate but not plumose in Geum). |
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x | = 8. |
= 7(8). |
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Aphanes |
Rosaceae subfam. rosoideae |
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Distribution |
North America; nw Mexico; Eurasia; n Africa [Introduced in s South America, Pacific Islands, Australia] |
North America; Mexico; Central America; South America; West Indies; Bermuda; Eurasia; Africa; Atlantic Islands; Indian Ocean Islands; Pacific Islands; Australia |
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Discussion | Species ca. 20 (3 in the flora). On the basis of molecular studies, R. Gehrke et al. (2008) have suggested that Aphanes and the Central America and South American Lachemilla (Focke) Rydberg should be included in a more broadly circumscribed Alchemilla. Both Aphanes and Lachemilla were shown to be monophyletic groups as is Alchemilla, apart from the African species currently placed in that genus; these form a clade separate from Alchemilla as represented in North America and Eurasia. The African species deserve more thorough investigation before such a morphologically distinct genus as Aphanes is abandoned. The highly reduced nature of plants of Aphanes, coupled with their high dispersibility, complicates circumscription of species in the genus. The most recent treatments recognize a number of endemic species in South America, Europe, and North Africa, particularly in regions with Mediterranean climates. The extent to which these, and those recognizable in western North America, represent native radiations versus multiple introductions remains to be determined. Measurements of flowers apply collectively to the length of the hypanthium and calyx measured in fruit. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Variation in the number of genera in subfam. Rosoideae is due to differences in generic delimitation between D. Potter et al. (2007) and the authors of some Potentilleae genera. Cyanogenic glycosides and sorbitol are absent in the subfamily. Tribes 6, genera 28–35, species ca. 1600 (6 tribes, 26 genera, 302 species, including 1 hybrid, in the flora) (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 9, p. 309. | FNA vol. 9, p. 23. | ||||||||
Parent taxa | ||||||||||
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Name authority | Linnaeus: Sp. Pl. 1: 123. (1753): Gen. Pl. ed. 5, 59. (1754) | Arnott: Botany, 107. (1832) | ||||||||
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