Prunus spinosa |
Prunus laurocerasus |
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blackthorn, blackthorn plum, sloe, sloe cherry |
cherry-laurel, common cherry laurel, hedge cherry laurel, laurel cherry |
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Habit | Shrubs, suckering, 10–40 dm, thorny. | Shrubs or trees, sometimes suckering, 20–60(–100) dm, not thorny. |
Twigs | with axillary end buds, hairy. |
with terminal end buds, glabrous. |
Leaves | deciduous; petiole 4–7 mm, hairy, eglandular; blade elliptic to obovate, 1.5–4 × 1–2.2 cm, base obtuse to rounded, margins crenulate-serrulate, teeth blunt, often glandular, apex acute to obtuse, abaxial surface hairy (especially along midribs and veins), adaxial glabrate. |
persistent; petiole 5–15 mm, glabrous, eglandular; blade elliptic to obovate, 6–18 × 3–7 cm, base cuneate to obtuse, margins remotely serrulate or nearly entire, teeth blunt, glandular, apex abruptly short-acuminate, apicula acute, surfaces glabrous, abaxial glandular, glands 1–several, proximal, flat, circular to oval. |
Inflorescences | usually solitary flowers, sometimes 2-flowered fascicles. |
26–32-flowered, racemes; central axes (35–)55–130 mm, leafless at bases. |
Pedicels | 0.5–5(–8) mm, usually glabrous, rarely hairy. |
1–5 mm, glabrous. |
Flowers | blooming before leaf emergence; hypanthium cupulate, 1.5–2.5 mm, glabrous externally; sepals spreading, oblong, 1.5–2.5 mm, margins glandular-toothed, surfaces glabrous or adaxially hairy at bases; petals white, elliptic, 4–8 mm; ovaries glabrous. |
blooming before leaf emergence; hypanthium cupulate, 3–4 mm, glabrous externally; sepals spreading, triangular, 0.7–1.2 mm, margins usually entire, sometimes with deciduous glands, ciliate in spots, surfaces glabrous or hairy; petals white, obovate or broadly elliptic to suborbiculate, 3–5 mm; ovaries glabrous. |
Drupes | bluish black, globose, 10–15 mm, glabrous; mesocarps fleshy; stones subglobose, ± flattened. |
deep purple-red to nearly black, ovoid to conic-ovoid, 13–17 mm, glabrous; mesocarps fleshy to leathery; stones ovoid, not flattened. |
2n | = 32. |
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Prunus spinosa |
Prunus laurocerasus |
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Phenology | Flowering Mar–May; fruiting Aug–Sep. | Flowering Mar–May; fruiting Aug–Nov. |
Habitat | Roadsides | Riparian thickets, shaded ravines, understory of urban and second-growth forests |
Elevation | 0–1000 m (0–3300 ft) | 0–600 m (0–2000 ft) |
Distribution |
CT; ID; MA; ME; MI; NY; OR; WA; BC; NS; ON; Eurasia; n Africa [Introduced in North America]
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CA; OR; WA; BC; Eurasia [Introduced in North America]
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Discussion | As past flora writers (C. L. Hitchcock et al. 1955–1969; E. G. Voss 1972–1996) have noted, the distinctions between Prunus spinosa and P. domestica are not clear. Some researchers consider the hexaploid P. domestica to have been derived from the tetraploid P. spinosa, often in a scenario involving hybridization with P. cerasifera. It should not be surprising that some of the characters used in keys to separate these three taxa (spininess, indument, leaf size, pedicel length, numbers of flowers per bud) are subject to variation within each species and overlap among the species. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Flowering specimens of Prunus laurocerasus with small leaves and entire margins that otherwise resemble P. caroliniana can be identified by their larger hypanthia and longer petals. In fruit, the stone is much harder in P. laurocerasus and does not split open upon drying; the flesh around the stone is thicker and more succulent. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 9, p. 376. | FNA vol. 9, p. 362. |
Parent taxa | Rosaceae > subfam. Amygdaloideae > tribe Amygdaleae > Prunus | Rosaceae > subfam. Amygdaloideae > tribe Amygdaleae > Prunus |
Sibling taxa | ||
Name authority | Linnaeus: Sp. Pl. 1: 475. (1753) | Linnaeus: Sp. Pl. 1: 474. (1753) |
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