Kindly sponsored by
Sir Henry Angest
Tom Christian (2025)
Recommended citation
Christian, T. (2025), 'Picea jezoensis' from the website Trees and Shrubs Online (treesandshrubsonline.
Tree to 50 m tall, <1.5 m dbh. Bark flaking from a young age, rough, scaly, blackish-brown to dark purplish-grey. Crown broadly conical to pyramidal. First order branches long, slender, spreading horizontally, lower branches downswept in old trees; second order branches dense, drooping or pendent. Branchlets short, slender, stiff, glossy, pale yellow at first, maturing orange-yellow to yellowish-brown (subsp. jezoensis) or reddish-brown (subsp. hondoensis), ridged and grooved, glabrous or puberulent; pulvini dense, angular, darker than 2nd year shoot. Vegetative buds ovoid-conical, 5–8 × 4–6 mm on leading shoots, not resinous; bud scales obtuse-triangular, orange-brown, glossy, persisting several years. Leaves radially spreading, directed strongly forwards above shoot, pectinate beneath, 10–20(–24) × 1.5–2(–2.2) mm, linear, slightly curved or more or less straight, obtriangular in cross section, apex acute or mucronate; stomata on lower surfaces in bands of 6–7 lines; leaf colour glossy dark green above, paler with two prominent stomatal bands beneath. Pollen cones to 1.5–2 cm, yellow. Seed cones numerous, often clustered, cylindrical to slightly curved, apex obtuse, (3–)4–7(–9) × 2–3.5 cm wide with opened scales, green at first, maturing through yellow to light or dark yellowish- or reddish-brown, occasionally pruinose. Seed scales numerous, small, obovate-oblong to nearly rhombic, very thin, papery, 1–1.2 × 0.6–0.8 cm at mid-cone; surface finely striated, usually undulate or smooth and flat, glabrous; upper margin undulate or erose-denticulate, base cuneate. Bracts ligulate with toothed and cuspidate apex, purplish, 4–5 mm long, entirely included. Seeds ovoid-cuneate, 3 × 2 mm, pale brown; seed wings ovate-oblong, 6–10 × 4–5 mm, yellowish-brown or orange-brown. (Farjon 2017; Grimshaw & Bayton 2009; Fu, Li & Mill 1999).
Distribution China Heilongjiang, Jilin, Nei Mongol Japan Hokkaido; N Honshu North Korea Russia Far eastern Siberia including Kamchatka, Kuril Islands, Sakhalin
Habitat Mountains and river basins from c. 40 m to 2500 m asl. Across an extensive range the species occurs in interior continental, maritime continental, and cold temperate climate zones with a broad range of associates. See infraspecific articles for further detail.
USDA Hardiness Zone 4-5
RHS Hardiness Rating H7
Conservation status Least concern (LC)
Taxonomic note The epithet jezoensis is derived from the former name for Hokkaido: Yezo or Jezo (Grimshaw & Bayton 2009).
Picea jezoensis is widely distributed in northeast Asia, from 59°N on the Kamchatka peninsula and c. 56°N on adjacent parts of mainland Russia south to Korea on the mainland and central Honshu in Japan; it extends westward as far as Russia’s Stanovoy Range and Aldan Highlands and China’s Nei Mongol province (Farjon 2017). This range takes in several climatic zones, including true continental in the interior parts of the mainland, cold maritime in coastal districts of the mainland and Kamchatka, Sakhalin, and the Kuril islands, where the proximity of the sea tempers the climate somewhat, cold maritime to cold temperate on Hokkaido, and cold to montane temperate on Honshu (Debreczy & Rácz 2011).
An extensive distribution across several climate zones has resulted in much morphological variation that taxonomists have sought to define, largely through the publication of infraspecific names, but as is so often the case in conifer taxonomy there has never been agreement on how many constituents should be recognised and at which rank(s). In the west, and particularly in Europe, Honshu’s populations have long been considered distinct, usually distinguished at the rank of variety (var. hondoensis) e.g. Dallimore & Jackson (1966), Bean (1981), Krüssmann (1985), and Rushforth (1987). Such a view owes as much to the relative ecological isolation of Honshu’s populations (and their suitability for cultivation in western Europe) as it does any morphological distinctiveness.
Further subdivisions, especially of continental populations, have been more contentious. Debreczy & Rácz (2011) recognised three varieties in addition to the type, viz. var. hondoensis, var. komarovii and var. microsperma. The latter was recognised in the Flora of China account (Fu, Li & Mill 1999) but otherwise receives little credence, usually being lumped with the type, while var. komarovii, described orignially at species rank in 1950, gained acceptance for a while (e.g. Farjon 1990). More recently, however, Plants of the World Online (2024) has relegated the various permutations of the name komarovii to the synonymy of Picea jezoensis var. koreana Uyeki published in 1942, some eight years prior to the publication of P. komarovii and therefore taking precedence, but only when the rank of variety is considered to be the most appropriate.
Over time, the relatively minor morphological differences these names were founded on have been shown to correlate to distinct geographical (and thus ecological) origins. This has led to a preference for the rank of subspecies which is now used in favour of variety by Farjon (2017) who treats subsp. hondoensis, endemic to Honshu, and subsp. jezoensis which makes up the rest of the distribution. Almost all modern works further subdivide subsp. jezoensis to include at least one variety, usually var. komarovii (now correctly var. koreana) but a 2010 study into variation in cone morphology concluded there was no sound basis for recognising any infraspecific taxa, not even for populations on Honshu (Park et al. 2010), but the study did not consider other characters, nor the relative isolation of Honshu material from the rest of the distribution.
On balance it seems that Farjon’s (2017) view is the most sensible course, particularly in a work with a strong horticultural focus, so we recognise subsp. hondoensis but treat all other populations as part of a wide ranging and variable single entity, subsp. jezoensis. Were a further taxon to be recognised it would be more logical to treat it at the rank of subspecies than variety, in which case the correct name would be subsp. komarovii (V.N.Vassil.) Silba, but the characters on which additional splits have traditionally been justified are not taxonomically significant.
In maritime parts of our area, including much of western Europe and especially the UK and Ireland, this species is represented almost exclusively by the Japanese endemic subsp. hondoensis which is better suited to the prevailing maritime climate. Subsp. jezoensis is occasionally grown in these regions but rarely if ever makes good trees; it is much better suited to cultivation in areas with a strongly continental climate, but even in such regions the type has only a limited presence in western cultivation. The cultivars listed below were mainly selected in western Europe or in the Pacific Northwest of North America; we therefore assume that these are selections of subsp. hondoensis and place them accordingly.
Picea jezoensis subsp. jezoensis seems to have gained something of an ugly duckling reputation compared with the Hondo Spruce, subsp. hondoensis, but this says less about the tree than it does about the dominance of British dendrological literature through much of the late 19th and early 20th centuries. Writing from a British perspective Bean (1976) dismissed subsp. jezoensis as probably absent from cultivation and unsuitable in the UK climate. Both subspecies were introduced to Britain in 1861 by John Gould Veitch while von Siebold introduced subsp. jezoensis to the Netherlands in the same year (Jacobson 1996). Both collectors gathered subsp. jezoensis on Hokkaido, and while the fate of material raised in Holland is unclear, Veitch found the taxon to be an abject failure in Britain where it soon died out, while plants of subsp. hondoensis largely thrived (albeit one batch was unfortunately mixed with P. alcoquiana, and for some while the Veitch Nurseries distributed Hondo Spruce under this name) (Mitchell 1972). Later introductions of subsp. jezoensis to Britain, by Maries from Hokkaido and Wilson from Korea, probably fared little better (Bean 1976).
G.R. Hall introduced subsp. jezoensis to North America in March 1862. Again the fate of those early introductions is unknown, but it stands to reason that it should have fared better in continental North America than it did in western Europe. New Trees reported that a Frank N. Meyer collection made in Russia had been maintained in North American cultivation; in the mid 2000s this was ‘represented by a grafted tree of 11 m (32.5 cm dbh) at the Morton Arboretum, derived from an original tree in the Arnold Arboretum’ but by 2024 the Morton’s online catalogue made no mention of it, suggesting the material has died out (Morton Arboretum 2024). There is no trace of a Meyer collection in the Arnold’s database, either, but subsp. jezoensis is at least represented there by multiple plants derived from collections traceable to Changbai County, Jilin, China (NACPEC 97037) and Sarobetsu National Park, Hokkaido, Japan (Nicholson & Hay s.n.), and there is a single plant introduced as var. komarovii under a 1995 accession (47–95*B, see images) gathered on the NACPEC Expedition to Heilongjiang under the number HLJ 098 (Arnold Arboretum 2024). The collection notes tell us the parent was growing in ‘Wet upland woods with Betula costata, Betula platyphylla var. mandshurica, Vitis amurensis, Alnus sibirica, Corylus sp.’ (Arnold Arboretum 2024).
Subsp. jezoensis grows well in those parts of Europe with a continental climate, for example in central Germany where a tree in Schlosspark, Wiesenburg, has reached 17 m × 50 cm dbh by July 2024, its identity confirmed by images showing the pale whitish-yellow shoot (Monumental Trees 2024). There is a plot of subsp. jezoensis at Arboretum Mustila, Finland, planted in 1936 with twelve-year-old trees raised from seed gathered in Hokkaido; both this and a plot of subsp. hondoensis are in good health (Arboretum Mustila 2024). In another part of the same arboretum, preliminary results of a provenance trial suggest that ‘young plants from seed from the [Changbai] Mountains, on the border between Manchuria and Korea, start to grow in spring rather later than plants from other sources, which makes them hardier to spring frosts’ (Arboretum Mustila 2024). Material was also introduced to European cultivation under the name var. komarovii, by the 1994 University of Helsinki Botanic Garden Excursion to China which collected it in Antu County, Jilin, China. Among the recipients of material was the Royal Botanic Garden Edinburgh which sent several young plants to Dawyck in the Scottish Borders under the accession number 19951160. This cold site is perhaps as close as one gets to a continental climate in the UK, but even here these plants have struggled and display a general lack of vigour – the best remained a stubborn 50 cm tall ten years after planting! (Royal Botanic Garden Edinburgh 2024; Tree Register 2024).
The western European experience, of very high mortality rates in conifers introduced from continental north east Asia, is now quite familiar. Writing in New Trees John Grimshaw coined the phrase ‘Siberian conifer syndrome’ to describe the problem, whereby late spring frosts frequently injure or kill vulnerable young growth. The result is a stunted bush that at best grows a few centimetres a year, but spends most of its life looking dreadful, locked in a war of attrition with the presiding curatror, the curator waiting for the tree to die, the tree daring the curator to do the sensible thing and dig it up and put it on the bonfire. Siberian Fir, Abies sibirica, is perhaps the poster child for this group, which also includes species such as A. sachalinensis, Larix sibirica and Pinus sibirica.
Naturally there are just enough exceptions to this rule to encourage over-optimistic experimentation whenever material is available. During research for New Trees in the early 2000s the Tree Register of Britain and Ireland listed only a single, mature plant of subsp. jezoensis (Grimshaw & Bayton 2009) but by 2024 this had increased to several, albeit many of the identifications are tentative and are based on the improbability of subsp. hondoensis performing so poorly in Britain as these suspect trees (Tree Register 2024). One such example, on the Fairburn Estate in the Scottish Highlands, is noted as having a bright orange shoot which confirms this does indeed represent subsp. hondoensis – the shoot colour (pale yellow to yellowish-brown cf. distinctly orange) is diagnostic. A handful of younger trees recorded by the Tree Register represent more recent introductions, notably EHOK 20 from Hokkaido which has grown well at Kew, of all places, where three healthy trees were all c. 5.5 m tall × 11 cm dbh in 2022 (Tree Register 2024), rather outperforming others there from Sakhalin (ESUS 176) (Grimshaw & Bayton 2009). It must be stressed, however, that these are exceptions that prove the rule; the Royal Botanic Garden Edinburgh has successfully killed dozens of plants of subsp. jezoensis from such diverse provenances as Hokkaido, Sakhalin, Kamchatka, Jilin, and even North Korea, planted in a diverse range of locations including Benmore and Dawyck Botanic Gardens, and safe sites participating in the International Conifer Conservation Programme (Royal Botanic Garden Edinburgh 2024).
Key to the subspecies of Picea jezoensis | ||
| 1a | Second year branchlets dark reddish-brown; leaves broad (1.8–2.2 mm wide) | subsp. hondoensis |
| 1b | Second year branchlets orange-yellow or yellowish-brown; leaves narrow (1.5–2 mm wide) | subsp. jezoensis |
Common Names
Hondo Spruce
Southern Yezo Spruce
Southern Jezo Spruce
Tōhi
Synonyms
Picea hondoensis Mayr
Picea jezoensis var. hondoensis (Mayr) Rehder
Pinus hondoensis (Mayr) Voss
Branchlets orange brown at first, dark reddish to orange brown in second year, later grey. Leaves flattened, broad-rhombic in cross-section, 8–15 × 1.8–2.2 mm. Seed cones 4–8 cm long; seed scales at midcone broadly obovate, flat, upper margin denticulate (Farjon 2017; Debreczy & Rácz 2011).
Distribution Japan Central Honshu and the Kii Peninsula
RHS Hardiness Rating: H7
USDA Hardiness Zone: 5
Like the type, Hondo Spruce was introduced to western cultivation by John Gould Veitch in 1861, albeit inadvertently. During an excursion to Mount Fuji local collectors assisting Veitch collected seed from both Picea jezoensis subsp. hondoensis and from P. alcoquiana, and the mixed bag was introduced under the latter name. It would take several years for the problem to be resolved, and for many years Hondo Spruce supplied by the Veitch nurseries were erroneously labelled P. alcoquiana (Elwes & Henry 1906–1913).
This error skewed early impressions of Picea alcoquiana in western Europe, which is actually rather slow-growing, whereas Hondo Spruce sustains an even rate of growth of between 30–45 cm per year for many decades once established (Mitchell 1972). This reliable performance was found to vary only slightly across the oceanic, but otherwise mercurial climate of Britain and Ireland; endowed also with great cold-hardiness Hondo Spruce was soon an essential addition to the Victorian pinetum and is still one of the more frequently met ‘unusual’ conifers in upland properties across this area (pers. obs.). Indeed, within collections and large gardens it was commonly planted, but in the wider landscape it remains curiously rare (Mitchell 1972; pers. obs.). The newly formed Forestry Commission and other British landowners experimented with forest plots of Hondo Spruce in the early 20th century, testing its suitability as a timber tree, but despite its climatic tolerances it never went mainstream (Wilson 2011).
That Hondo Spruce is so well suited to the maritime climate of western Europe, where the type is usually an abject failure, has done much to bolster the Anglo- (or at least Euro-) centric view that it merits taxonomic distinction. Many observers, from Wilson to the present day, could find no justification for recognising it as distinct and would treat all populations within a single, variable, wide-ranging species (Wilson 1916; Park et al. 2010) but European growers have always benefitted from a means to differentiate this more appropriate ecotype.
The tallest tree on record in Britain is one since lost that grew at Eridge Park, Tunbridge Wells; in 1984 it was 33 m tall × 91 cm dbh. The tallest extant trees are 32.4 m × 86 cm at Kiltegan, Wicklow, Ireland, and another 31 m at Tollymore Forest Park, County Down, and several more over 30 m from Devon to the Scottish Highlands. An excellent tree with a long history of measurement grows near the head of the famous Sequoiadendron avenue at Benmore Botanic Garden, Argyll; planted in 1880 it was 15.8 m tall × 0.42 m dbh in 1905; 24.4 m × 1.04 m in 1980; and 29.5 m × 1.18 m in 2017, making it the current UK and Ireland champion for girth (Tree Register 2024; Clarke 1988; Elwes & Henry 1906–1913).
Confirmed records from Europe and North America are scarce. In many cases databases simply list ‘Picea jezoensis’ and particularly in continental climate zone collections accessions under this name usually represent the type (e.g. Arnold Arboretum 2024; Morton Arboretum 2024). A handful are recorded from Belgium, the Netherlands, Germany, and are probably scattered through most other European collections, though here as in North America the type would seem to be the more common (Arboretum Wespelaar 2024; Monumental Trees 2024).
An old selection raised in Germany in 1891, with young growth golden-yellow, later maturing through yellowish green to brownish green. Best in light shade, according to Auders & Spicer (2012).
A slow-growing, compact, rather globose shrub, to 70 cm tall and wide in ten years. Listed by the Horstmann Nurseries, Germany, in 1992 (Auders & Spicer 2012). If the rather unusual cultivar name is interpreted to indicate Chinese origin, then this cultivar would belong to the nominate subspecies, not subsp. hondoensis.
A dense bush of broadly globose habit, usually flat-topped, with glaucous-green leaves. To 60 cm tall and broad after ten years. First listed in 1988 by the Mitsch Nursery, Oregon (Auders & Spicer 2012).
Synonyms / alternative names
Picea jezoensis 'D.J. Broom'
A compact dwarf to 50–60 cm tall and broad after ten years. Listed by the Oregon firm Bucholz & Bucholz in 2009 (Auders & Spicer 2012)
A slow-growing, dwarf selection listed by the Horstmann Nurseries, Germany, in 1992 (Auders & Spicer 2012).
A narrowly conical selection, to 1.2 m tall but only half as broad in ten years. Listed by G. Bentham, Canada in 1981 (Auders & Spicer 2012).
A flat-topped bush of somewhat irregular habit, to 40 cm tall and 60 cm across after ten years. The bluish needles are radially arranged on leading shoots. Listed by Edwin Smits in the Netherlands in 2009 (Auders & Spicer 2012).
A broadly pyramidal selection of dense habit bearing glaucous-grey leaves, up to 1 m tall after ten years but usually less. Reported from the United States before 1996 but the Latin cultivar name is only valid if it can be proven to have been published before 1959 (Auders & Spicer 2012).
A pyramidal plant of rather open habit, bearing ‘yellowish blue-green foliage’. To 1.5 m tall and 1 m across in ten years. Listed by Bucholz & Bucholz of Oregon in 2009 (Auders & Spicer 2012). This might represent Picea glehnii.
An irregularly globose dwarf growing to c. 60 cm tall and broad in ten years, the young spring growth yellow. Raised in Japan, introduced first to Canada in 1980 and thence from the Alpenglow Gardens to the Iseli Nurseries in Oregon, United States (Auders & Spicer 2012). Like ‘Chitosemaru’ and ‘Shimizusei’, it might represent Picea glehnii.
Originating from a witches’ broom and commercialised by the Horstmann Nurseries, Germany in 1983, this selection forms a pyramidal plant with particularly glaucous foliage. To 1.5 m tall after ten years (Auders & Spicer 2012).