Malus |
Malus hupehensis |
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apple, crabapple, pommier |
Chinese crab apple, flowering tea crabapple, tea crabapple, tea or flowering tea crabapple |
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Habit | Shrubs or trees, 2–200 dm. | Trees, to 80 dm. | ||||||||||||||||||||||||||||||||||||
Stems | 1+ (derived from root shoots), erect; bark dark brown, reddish brown, or gray, firm, platy or scaly; long and short shoots present; thorns present (modified short shoots); glabrous, glabrescent, villous, densely puberulent, or tomentose. |
to 30 cm diam.; bark dark gray or dark brown, smooth or rough; young branches dark green and puberulous, becoming purplish or purplish brown and glabrous at maturity; flowering shoots developing as spurs, 5–20(–40) mm. |
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Buds | dark purple, ovoid, 3–4(–5) mm, scale margins sparsely ciliate. |
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Leaves | deciduous [semipersistent], cauline, simple, shoot dimorphism, long- and juvenile-shoot leaves usually larger and more deeply serrate (lobed) than short-shoot leaves; stipules deciduous (or persistent on vigorous shoot leaves in M. baccata), basally adnate to petiole, linear-lanceolate to lanceolate, sometimes filiform, membranous, sometimes herbaceous, margins entire, serrulate, glandular-serrate, sparsely glandular-denticulate, or white-ciliate; petiole present; blade elliptic, ovate, obovate, triangular-ovate, oval, lanceolate, ovate-oblong, or oblong, (2–)4–12 cm, membranous or leathery, margins flat, sometimes lobed, dentate, serrulate, serrate, doubly serrate, crenate, or sometimes entire, venation pinnate (craspedodromous when lobed, camptodromous when unlobed), surfaces glabrous or tomentose. |
convolute in bud; isomorphic; stipules deciduous, linear-lanceolate, 5–6 mm, apex acuminate; petiole 10–30 mm, sparsely pubescent when young, glabrescent; blade ovate or ovate-oblong, 5–10 × 2.4–4 cm, base broadly cuneate, rarely rounded, margins unlobed, sharply serrulate, apex acuminate, surfaces sparsely puberulent when young, becoming glabrous. |
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Panicles | umbel-like; peduncles absent; bracteoles rarely persistent, lanceolate, 2 mm. |
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Inflorescences | terminal on short shoots, 2–12-flowered, flat-topped panicles, glabrous or tomentose; bracts present (absent in M. fusca), caducous, ovate, linear-lanceolate, membranous, glabrous; bracteoles present. |
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Pedicels | present. |
30–40 mm, glabrous or slightly villous. |
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Flowers | bisexual (occasionally andromonoecious in M. halliana), opening with leaves, perianth and androecium epigynous, 15–50 mm diam.; hypanthium campanulate, size not recorded, glabrous or tomentose; sepals 5, reflexed to wide spreading, triangular, triangular-lanceolate, triangular-ovate, or lanceolate; petals 5 (or more in M. halliana), white, pink, or red, suborbiculate, obovate, narrowly or oblong-obovate, ovate, or ± elliptic, base clawed; stamens 15–50, unequal, usually shorter than, rarely equal to, petals; carpels 3–5, connate, adnate to hypanthium, styles 3–5, emerge from base of hypanthium, basally connate, glabrous or tomentose basally; ovules 2. |
35–40 mm diam.; hypanthium constricted distal to ovaries, glabrous or sparsely villous; sepals triangular-ovate, 4–5 mm, equal to or shorter than tube, apex acute or acuminate, abaxial surface glabrous, adaxial hairy; petals white, sometimes pink-white, obovate, 15 mm, claws 1 mm, margins crenulate, apex rounded; stamens 20, 6–8 mm, anthers white before dehiscence; styles 3(or 4), basally connate to 1/2 length, 7–9 mm, slightly longer than stamens, proximally tomentose. |
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Fruits | pomes, green, yellow, or red, globose, depressed-globose, obovoid, or oblong, 6–50(–70) mm diam., glaucous, waxy, punctate; flesh homogeneous, stone cells adjacent to carpels and epidermis; hypanthium persistent; sepals persistent or deciduous, erect or reflexed; carpels cartilaginous; styles persistent or deciduous. |
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Pomes | greenish yellow with red blush, ellipsoid or subglobose, 10 mm diam., cores enclosed at apex; sepals deciduous; sclereids sparse to moderate surrounding core. |
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Seeds | 2 per carpel, light, dark, or reddish brown, smooth. |
brown. |
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x | = 17. |
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2n | = 51, 68. |
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Malus |
Malus hupehensis |
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Phenology | Flowering Apr–May; fruiting Aug–Sep. | |||||||||||||||||||||||||||||||||||||
Habitat | Slopes and valleys | |||||||||||||||||||||||||||||||||||||
Elevation | 0–2900 m (0–9500 ft) | |||||||||||||||||||||||||||||||||||||
Distribution |
North America; Eurasia [Introduced widely, especially in temperate regions] |
IL; WA; Asia [Introduced in North America; introduced also in Europe] |
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Discussion | Species 25–55 (10 in the flora). Malus has great economic value; species are widely cultivated throughout the world for their edible fruit (not all species), ornamental fruit, or flowers. Mammals and birds eat cultivated and wild apples, which can result in the spread of seed and naturalization of species. The hard wood is occasionally used to make furniture and tools, and as fuel. The apple has symbolic significance in western cultures, including Greek, Roman, and Judeo-Christian mythologies. The apple often represents desire, temptation, and sin in art and literature (malum is Latin for evil), symbolizing sexuality, love, and the forbidden fruit of the Garden of Eden. Cross-compatibility among species is common. Hybridization can occur naturally in botanical gardens and in the wild, or artificially through breeding. Polyploid forms and asexual seed production (apomixis) occur in some species. The taxonomy of Malus has been revised at least three times, with some authors placing species within the genus Pyrus. Recent morphologic work has suggested that Malus be retained as a separate genus based on fully adnate carpels and deeply inferior ovaries (K. R. Robertson et al. 1991), with molecular evidence providing support (C. S. Campbell et al. 1995). Cultivation, hybridization, and introgression have led to hundreds of species names within Malus. The genus requires a comprehensive worldwide revision. The eastern North American apples stand apart from other members of the genus by having unique floral and fruit traits, which define sect. Chloromeles (Decaisne) Rehder. Although distinctive morphologic extremes are obvious, continuous variation within this overall homogeneous group blurs species boundaries. Historically, taxonomic confusion has resulted from names being applied to slight variations in: leaf lobing and serration; patterns of leaf venation; leaf, calyx, and pedicel indument; and fruit shape. Leaves of vigorous long shoots often differ in shape and hairiness from those of short flowering shoots on the same tree. Polyploidy and apomixis may contribute to taxonomic difficulties by locking suites of traits together into morphologic forms. Morphologic patterns within the group can shift. Studies indicate that diploids within natural populations occasionally produce triploid and tetraploid progeny; triploids can give rise to tetraploids (E. E. Dickson 1995). Preliminary genetic studies do not clarify species boundaries and suggest a single monotypic species, Malus coronaria (Dickson et al. 1991; Dickson 1995). This treatment takes a conservative approach by recognizing three morphologic extremes as species. Further work is warranted to clarify the taxonomy of sect. Chloromeles. The description of Malus prunifolia is based on Y. Asami (1927) and Gu C. Z. and S. A. Spongberg (2003); M. baccata and M. halliana are based on Gu and Spongberg; M. hupehensis is based on Gu and Spongberg and C. A. Huckins 1972; and M. toringo (as M. sieboldii) is based on Asami, Huckins, and Gu and Spongberg. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Malus hupehensis is possibly naturalized in Egypt. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 9, p. 472. | FNA vol. 9, p. 478. | ||||||||||||||||||||||||||||||||||||
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Synonyms | Pyrus hupehensis, M. domestica var. hupehensis, M. theifera | |||||||||||||||||||||||||||||||||||||
Name authority | Miller: Gard. Dict. Abr. ed. 4, vol. 2. (1754) | (Pampanini) Rehder: J. Arnold Arbor. 14: 207. (1933) | ||||||||||||||||||||||||||||||||||||
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