Betula cylindrostachya Lindl. ex Wall.

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Sponsor

Kindly sponsored by the Banks family in memory of Lawrence Banks CBE DL VMH

Credits

Hugh A. McAllister, Kenneth Ashburner, Paul Bartlett & Martin Deasy (2026)

Recommended citation
McAllister, H. A., Ashburner, K., Bartlett, P. & Deasy M. (2026), 'Betula cylindrostachya' from the website Trees and Shrubs Online (treesandshrubsonline.org/articles/betula/betula-cylindrostachya/). Accessed 2026-07-16.

Family

  • Betulaceae

Genus

  • Betula
  • Subgenus Acuminatae section Acuminatae

Synonyms

  • Betula alnoides var. cylindrostachya (Wall.) H.J.P.Winkl.
  • Betula rhombibracteata P.C.Li
  • Betulaster cylindrostachya (Wall.) Spach
  • Betula fujianensis J.Zeng, Jian H.Li & Z.D.Chen
  • Betula acuminata var. cylindrostachya (Wall.) Regel
  • Betula cylindrostachya var. typica Regel

Glossary

Tibet
Traditional English name for the formerly independent state known to its people as Bod now the Tibet (Xizang) Autonomous Region of the People’s Republic of China. The name Xizang is used in lists of Chinese provinces.
abaxial
(especially of surface of a leaf) Lower; facing away from the axis. (Cf. adaxial.)
bud
Immature shoot protected by scales that develops into leaves and/or flowers.
glandular
Bearing glands.
nutlet
Small nut. Term may also be applied to an achene or part of a schizocarp.
ovate
Egg-shaped; broadest towards the stem.

Credits

Hugh A. McAllister, Kenneth Ashburner, Paul Bartlett & Martin Deasy (2026)

Recommended citation
McAllister, H. A., Ashburner, K., Bartlett, P. & Deasy M. (2026), 'Betula cylindrostachya' from the website Trees and Shrubs Online (treesandshrubsonline.org/articles/betula/betula-cylindrostachya/). Accessed 2026-07-16.

Editorial Note

This TSO article is an edited digest of the species account in Kenneth Ashburner and Hugh McAllister, The Genus Betula: A Taxonomic Revision of Birches (2013; repr. 2016).

Trees and Shrubs Online, 23 June 2026

Tree to 30 m. Bark dark brown. Twig light brown, to 3 mm in diam., glabrescent. Buds c. 9–11 × 3.5 mm, ovate, acuminate, incurved. Shoots mostly densely white hairy, eglandular or with some glands on the very youngest part, rarely very glandular. Petioles 0.8–1.5 cm, hairy, glandular; petiole:blade ratio c. 1:10. Leaves ovate-elliptic, oblong to ovate-lanceolate, (5)–14 × 2–8 cm, base rounded or sub-cordate, apex acuminate, margin serrate, with 13–14(–15) pairs of secondary veins ending in prominent teeth with up to 7 teeth between these, hairy when young on both surfaces and glandular below (abaxially), persistently hairy in secondary vein axils. Male catkins to 60 × 3 mm, scales peltate, often apiculate, c. 2 × 2 mm. Fruiting catkins usually in groups of 2 or 3, or solitary; peduncle to 20 mm, hairy; catkins to 100 × 5–7(–10) mm; transitional region between peduncle and catkin proper c. 5 mm, with small poorly developed scales and fruitlets. Scales 2–3.25 × 1.5–1.7 mm, base very thick, lobes very thin and acute, laterals much reduced c. 1/3 length of midlobe. Seeds to 2.5 × 4.5 mm usually narrowing towards base, nutlet 2–2.25 × 1–1.5 mm, usually broadest towards apex; style c. 1.75 mm. Tetraploid: 2n=56. Flowering time. March to May. Fruiting. May to June.

Distribution  BhutanMyanmar north China southwest Sichuan, northwest Yunnan, Fujian India Himachal Pradesh (Beas river valley), Sikkim, Darjeeling district, Assam (Khasia Hills) NepalPakistan Chitral

Habitat Subtropical to warm-temperate broadleaved forest at 1000–3000 m asl.; river valleys, often in disturbed ground.

USDA Hardiness Zone 9

Conservation status Least concern (LC)

Taxonomic note Betula luminifera is morphologically very similar, but has (usually) solitary female catkins (groups of two to six catkins in the other two).

Described by John Lindley (in Wallich 1831) from specimens collected in Uttarakhand, northern India, Betula cylindrostachya is a component of the warm temperate broad-leaved Himalayan forests, its range and altitudinal distribution overlapping with that of Betula alnoides, with which it has been (and continues to be) much confused. The two species often grow in close proximity (Skvortsov 1997) and can occupy similar habitats, but B. cylindrostachya flowers in spring, while Betula alnoides is autumn-flowering and more markedly subtropical in character. Nevertheless, many collectors and observers have not distinguished between the two taxa and they remain widely confused – most recent introductions to cultivation in Britain named Betula alnoides appear to be B. cylindrostachya, helpfully found to be tetraploid in contrast to the reportedly diploid B. alnoides (Mehra & Sareen 1973). In the field the most useful distinguishing characters are probably the spring flowering time (rather than autumn to winter), larger nutlets, much more closely toothed leaf margin, and the hairy and usually almost eglandular young shoots (note, however, that the glands may be difficult to detect under the dense hair, and glandular specimens might be referable to B. alnoides or possibly hybrids). For a table enumerating the distinguishing features, see the entry for B. alnoides.

As a low-altitude, southerly species, Betula cylindrostachya is less hardy than most birches – like other members of subgenus Acuminatae it is unable to fall back on dormant buds to replace new growth damaged by late spring frost or dessicating winds: the buds on young trees break simultaneously, and if these are killed the trees appear to be incapable of generating new buds from the base of their trunks. Probably for this reason, the species is rather rare in cultivation outside its native area, though it promises to be an attractive horticultural subject for warmer temperate climates. In mild, coastal districts, young trees grow rapidly to form large spreading trees – two plants raised from a collection by Peter Cox and Steve Hootman (C&H 9042) have thrived at Tregrehan, Cornwall, reaching 10 m by 2007, with attractive dark brown, shiny trunks, and long showy catkins in early spring (T. Hudson, cited in Grimshaw & Bayton 2009). This collection is also grown at Howick Arboretum, Northumberland. Keith Rushforth’s collections of B. cylindrostachya from Bhutan (KR 876, 976) and Tibet (KR 6000) and Kenneth Ashburner’s north Indian introduction from Garhwal have survived without significant damage for more than ten years at Ness Botanic Garden, forming vigorous spreading, freely fruiting trees which look as if they may eventually grow large and attractive. Given the species’ role as a primary coloniser in its native habitat, the possibility that it could naturalise and become invasive should be borne in mind.

Any batch of seedlings shows a range of variation in time of bud break, and those with later breaking buds may be the only ones that survive late frosts and wind damage in extrazonal temperate conditions. The possibility of selecting strains of Betula cylindrostachya adapted to higher latitude temperate climates is therefore worth serious attention. At Ness, for example, material originating from Garhwal seed has undergone natural selection, many plants having died at the seedling stage from late frosts. Additionally, as noted by Hacke & Sauter (1996) in a discussion on timing of bud break, epigenetic factors – that is, inherited characteristics affecting gene expession but not involving changes in DNA – may result in trees grown from seed from cultivated trees being less susceptible to frost damage than trees grown in the same area from seed of wild origin. Now that B. cylindrostachya is fruiting in western temperate collections it may be possible to produce seedlings adapted to higher latitudes.

The only difference between type Betula cylindrostachya and the relatively recently described B. fujianensis (Zeng, Li & Chen 2008) – treated in synonymy by McAllister and Ashburner (2013) – seems to be the glandular shoots and absence of hair tufts in the secondary vein axils on the abaxial leaf surface (both variable characters in B. cylindrostachya). These Fujianese populations had previously been regarded as B. alnoides (Li & Skvortsov 1999; Zeng, Li & Chen 2008), but the deciduous character, spring flowering, densely hairy young shoots, often subcordate leaf base, suborbicular to ovate nutlet, and greater hardiness reported by Zeng, Li and Chen led those authors to deduce that they did not belong to that species and they described them as a new species, B. fujianensis, which they compared with B. alnoides and B. luminifera but not B. cylindrostachya.