Sorbus |
Sorbus hybrida |
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alisier, mountain-ash, rowan, service tree, sorbier, whitebeam |
hybrid mountain ash, oak-leaf mountain-ash, Swedish mountain-ash, Swedish service-tree |
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Habit | Shrubs or trees, 10–300 dm. | Trees, 30–120 dm. | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Stems | 1–8, erect or ascending; bark gray to brown or bronze, usually smooth, becoming scaly with age, with conspicuous horizontal lenticels; long and short shoots present; unarmed; twigs with smell and taste of bitter almond (cyanogenic glycosides); glabrous or hairy. |
single or multistemmed; bark gray; winter buds brownish to purple, ovoid to ovoid-conic, 4–10 mm, dull, not glutinous, densely white-villous, at least distally and on scale margins. |
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Leaves | deciduous, cauline, simple or odd (rarely even) pinnately lobed or divided; stipules usually early deciduous, sometimes persistent, free or short-adnate to petiole, linear, ovate to lanceolate, or flabellate, margins entire or dentate to laciniate; petiole present; blade ovate to oblong, 5–33 cm, membranous to slightly leathery, leaflets 0 or 7–17(–19), usually opposite, rarely alternate, elliptic, ovate, oblong to lanceolate or oblanceolate, margins flat, sharply serrate to nearly entire, venation pinnate, surfaces glabrous or hairy, sometimes glaucous. |
proximally pinnately compound, lobed distally; stipules deciduous or persistent, often white-villous; blade paler green abaxially, dull green adaxially, ovate to oblong-ovate, rarely oblong, 7–13 × 5–11 cm, pinnately lobed with (1 or)2(or 3) pairs of sessile or decurrent, free, oblong leaflets, terminal leaflets 7–10-lobed, margins serrate at least distally, lobe and leaflet apex acute or obtuse, lateral veins 7–10 pairs, abaxial surface whitish-tomentose. |
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Panicles | 25–75-flowered, flat-topped or rounded, 4.5–10 cm diam.; peduncles white-villous. |
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Inflorescences | terminal, 6–400+-flowered, panicles, flat-topped or rounded, glabrous, glaucous, or hairy; bracts present; bracteoles absent. |
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Pedicels | present. |
white-villous. |
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Flowers | opening after leaf expansion, perianth and androecium epigynous or 1/2 epigynous, odor strong, often considered unpleasant or rancid, 5–17 mm diam.; hypanthium green to red, obconic, 2–6 mm, glabrous or hairy; sepals 5, erect or ascending, ovate or triangular; petals 5, white or pink [red], suborbiculate or broadly obovate to broadly ovate, base clawed or not, claw often ± villous; stamens [10–]14–20[–44] in 2 or 3 series, usually slightly longer than petals; carpels 2–5, distinct, partially or wholly connate and adnate to all or proximal 1/2 of hypanthium, usually apically woolly, styles 2–5, terminal, distinct or connate 1/2 of length; ovules 2 or 3[or 4] (all but 1 usually aborting). |
10–15 mm diam.; hypanthium tomentose, hypanthium plus sepals 5–7.5 mm; sepals 1.5–4 mm, margins usually entire, rarely with inconspicuous glands; petals white, suborbiculate, broadly obovate, broadly ovate, or broadly elliptic, 5–7 mm; stamens 20; carpels 1/2 adnate to hypanthium, apex conic, styles 2 or 3, 2–3 mm. |
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Infructescences | glabrate to villous. |
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Fruits | pomes, usually orange or red, rarely brown or yellow [green, white, or pink], globose to ovoid, obovoid, ellipsoid, or oblong, [pyriform], 4–19 mm, smooth or with lenticels, shiny, sometimes glaucous, hairy or glabrous; flesh usually with sclereids; hypanthium persistent; sepals usually persistent, rarely deciduous, usually incurved, fleshy; carpels cartilaginous; styles often persistent. |
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Pomes | red, globose to subglobose, 8–15 mm diam., shiny, not glaucous; sepals inconspicuous, incurved. |
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Seeds | 3–5, brown to reddish brown or yellowish, darkening with maturity, ovoid to lanceoloid, slightly asymmetric and flattened. |
red-brown, ovoid, 5–6 × 2 mm, asymmetric, slightly flattened. |
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x | = 17. |
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2n | = 68. |
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Sorbus |
Sorbus hybrida |
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Phenology | Flowering spring; fruiting fall. | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Woods, rocky slopes, disturbed ground and edges near towns | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 0–1000 m (0–3300 ft) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
North America; Eurasia; n Africa; Atlantic Islands; Pacific Islands |
UT; VT; WA; NB; n Europe [Introduced in North America]
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Discussion | Species ca. 130 (10 in the flora). The taxonomy of Sorbus is complicated by apomixis, polyploidy, and hybridization among sections and genera, especially in Eurasia. Hybrids with other genera in Maleae are generally distinguished by their incompletely divided, deeply lobed leaves, and include ×Amelasorbus Rehder (Sorbus × Amelanchier), ×Crataegosorbus Makino (Sorbus × Crataegus), ×Sorbaronia C. K. Schneider (Sorbus × Aronia), ×Sorbocotoneaster Pojarkova (Sorbus × Cotoneaster), ×Sorbopyrus C. K. Schneider (Sorbus × Pyrus), and ×Tormimalus Holub (as Torminalis Medikus [= Sorbus subg. Torminaria] × Malus). Only ×Amelasorbus and ×Sorbaronia are known to occur naturally in North America. Parentages of some reported ×Sorbaronia nothospecies are difficult to verify, especially for densely hairy hybrids involving either Aronia arbutifolia, A. ×prunifolia (Marshall) Rehder, or Sorbus aucuparia; all these possibilities are claimed. In addition to their partially pinnate leaves, some ×Sorbaronia hybrids may be recognized by the presence of pink to red anthers and black or purple fruits; these are reported also to be somewhat sterile. Diploid Sorbus are often obligate outcrossers; some apomictic triploids and tetraploids are self-compatible (C. S. Campbell et al. 1991; H. A. McAllister 2005). Some species have morphologically indistinguishable diploid and tetraploid races, with sexual and apomictic individuals. North American species are in need of biosystematic review. Sorbus is treated here in the broad sense, as a provisional arrangement to accommodate more than 70 natural hybrids between simple- and pinnate-leaved subgenera (J. B. Phipps et al. 1990; E. B. Nelson-Jones et al. 2002; C. Kalkman 2004; A. Robertson et al. 2004, 2004b; J. J. Aldasoro et al. 2004, 2005). Additional hybrid taxa continue to be discovered in Europe (G. Aas et al. 1994; M. F. Fay et al. 2002; T. C. G. Rich and L. Houston 2006; A. Robertson and C. Sydes 2006). Nonetheless, the argument has been made to revive generic ranking for the simple-leaved subgenera Aria and Torminaria, based on flower and fruit characters (K. R. Robertson et al. 1991), with some support from molecular investigations (C. S. Campbell et al. 1995, 2007; D. Potter et al. 2007). Subgenus Torminaria is anomalous in Sorbus, having a unique flavonoid chemistry, leaves with relatively few broad lobes, and scented brown fruits, thick-skinned as in subg. Cormus (Spach) Duchartre and some Pyrus, and being dispersed by carnivorous mammals as well as birds (C. M. Herrera 1987, 1989). Eurasian hybrids between subgenera frequently involve S. torminalis of subg. Torminaria. Subgenera Aria and Torminaria are likely to be recognized at generic rank once molecular studies can consistently resolve their placement within the Pyrinae, overcoming current difficulties with interfertility, reticulate relationships, rapid radiation, and small samples (Campbell et al. 2007; Potter et al.). Some species of Sorbus are cultivated as ornamentals. The colorful fruits of native and introduced species persist after the leaves drop and are consumed by birds across North America (A. C. Martin et al. 1951). One exotic species disseminated by birds is invasive (S. aucuparia). The pomes of S. americana, collected after a frost, can be sweetened for preserves. The pulp of some strains of S. aucuparia is reported to be less bitter. It may be eaten fresh or dried or used as flour. The fruits of a number of Eurasian species are made into vinegar, spirits, or medications. Sorbus domestica and S. torminalis pomes are sometimes eaten after being bletted (allowed to autodigest and become soft and mushy in texture). The fine-grained wood of Sorbus is used for carving or furniture in China. The bark of some species is antiseptic, or used to tan leather. Sorbus sambucifolia pomes show some potential in early testing for treating tumors (Y. Yoshizawa et al. 2000, 2000b). In order to identify intergeneric hybrids involving Sorbus as one of the parents, the following key includes leads for ×Amelasorbus and ×Sorbaronia. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Sorbus hybrida is considered an apomictic tetraploid producing fully fertile pollen and seed and subject to dispersal. An almost undistinguishable European taxon, S. ×thuringiaca (Ilse) Fritsch, often confused with S. hybrida, has been reported for New Hampshire and Vermont. Described as an unstable diploid hybrid between S. aria and S. aucuparia, S. ×thuringiaca has oblong leaves, 1–3(–5) pairs of free leaflets, 10–12(–13) pairs of lateral veins, and produces sterile pollen and relatively few viable seeds. Uncritical reports of escaped S. ×thuringiaca in North America should be considered doubtful; they probably refer to the more likely S. hybrida. The authors have not seen a specimen to document a report of S. hybrida from Montana. Sorbus hybrida is placed in subg. Sorbus following J. J. Aldasoro et al. (2004), based on leaf division and pome characteristics, including the lack of tanniferous cells in parenchyma, lack of starch, and relatively small sclereid groups. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key | Key to sub-genera of Sorbus
In order to identify intergeneric hybrids involving Sorbus as one of the parents, the following key includes leads for ×Amelasorbus and ×Sorbaronia.
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Source | FNA vol. 9, p. 433. | FNA vol. 9, p. 438. | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Name authority | Linnaeus: Sp. Pl. 1: 477. (1753): Gen. Pl. ed. 5, 213. (1754) | Linnaeus: Sp. Pl. ed. 2, 1: 684. (1762) | ||||||||||||||||||||||||||||||||||||||||||||||||||||
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