Fagus crenata

Last updated

Japanese beech
Fagus crenata in Ogasayama 2010-10-17.jpg
Fagus crenata in Toyama Prefecture during autumn
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Fagales
Family: Fagaceae
Genus: Fagus
Species:
F. crenata
Binomial name
Fagus crenata
Blume, 1851
Synonyms

Fagus ferruginea (invalid) [2]
Fagus sieboldii

Fagus crenata, buna (Japanese: ブナ), known as Siebold's beech, or Japanese beech, is a species of deciduous tree in the family Fagaceae. It is a tall dense hardwood that is only native to Japan. The first written record of this tree in the Western world was in 1830 and it was scientifically described in 1851. It is a high canopy tree and is the dominant tree in most of its range; often colocated with Quercus crispula [a] (Japanese oak) and Acer mono (Painted maple). Nuts, seeds, oil, and young leaves can be eaten but care must be exercised due to toxins. It is also used for firewood, furniture, construction, and shade. Climate change is having a negative impact on this tree.

Contents

Description

Fagus crenata reaches 35 meters (115 ft) in height. The crown is rounded with thick low branches and the bark is smooth and light-grey to white with mottled pale gray, dark gray, and greenish-gray. Buttress roots often grow. Surface roots may also develop to obtain more oxygen. The simple leaves are arranged alternately along the branch, growing 7.5 to 15 centimeters (3.0 to 5.9 in) long and 2.5 to 8 centimeters (0.98 to 3.15 in) wide. [4] The leaves are serrated and obovate. They are broadest towards the base and have 7-11 pairs of veins. In fall the leaves are rusty red, yellow, and brown. [5]

The nut is 3-winged and has a short thick stalk, 15 millimeters (0.6 in) long and is inside a spiny husk. [5] [4] The nuts are edible when ripe but are toxic to humans if eaten raw, due to saponic glycoside causing stomach problems. [4] There are flattened green whiskers at the base of the husk of the nut. [5] Seeds are dispersed by synzoochory via rodents and birds. [6] The flowers are small, wind-pollinated, and monoecious and allogamous. [5] [6] Its growth rate is very slow. [5] F. crenata tolerates acid, neutral, and alkaline soils but grows best in well-drained loamy and sandy soil. While it can grow in deep shade, it prefers full sun and hot summers. [5]

Taxonomy

Fagus ferrugineaAiton was first mentiond by Philipp Franz von Siebold in 1830 but it was only briefly mentioned and not scientifically described. [7] [8] [9] Siebold and colleagues published Flora Japonica in two volumes and thirty parts from 1835-1870, but did not mention F. crenata nor F. ferruginea. [10] [11] [12] Previously, F. ferruginea was used to refer to both F. crenata and Fagus grandifolia . Due to the resulting confusion, F. ferruginea ceased being used. [13] [14]

Fagus sieboldii is an accepted synonym of F. crenata in recognition of Siebold's extensive work on Japanese flora. [13] [15] This designation was first used by Stephan Endlicher in 1847. [16] [b]

Fagus crenata Blume was first scientifically described by Carl Ludwig Blume in 1851. [13] Fagus is subdivided into two subgenera: Engleriana, which are low-branching with yellowish bark, and Fagus, which is high-branching with light-grey bark. Another species of beech is found in Japan, Fagus japonica , which is in subgenus Engleriana while F. crenata is in the subgenus Fagus. [17] [18] [19]

Common names for F. crenata include its Japanese name buna (Japanese: ブナ), [20] , Siebold's beech, and Japanese beech. [4]

Etymology

Fagus crenata in winter Fagus crenata and snow in Mount Sanpokuzure 2011-04-10.jpg
Fagus crenata in winter

The common name of "beech" is from the Anglo-Saxon boc, bece or beoce, the German buche, the Swedish box - all meaning "book" as well as beech and derived from the Sanskrit boko or letter and bokos or writings. This connection to "beech" seems to have derived from the fact that the old Runic tablets were made of beech wood. [21]

The name of the tree genus in Latin, fagus, is cognate with English "beech" and of Indo-European origin. It played a role in early debates on the geographical origins of the Indo-European people, the beech argument. Greek φηγός (figós) is from the same root, but the word was transferred to the oak tree (e.g. Iliad 16.767) as a result of the absence of beech trees in southern Greece. [22] Crenulata comes from the Latin crenus, meaning "notch", because the leaves have small round teeth. [23]

Distribution and habitat

Fagus crenata native distribution map in Japan Fagus crenata native distribution-v2.jpg
Fagus crenata native distribution map in Japan

Fagus crenata is endemic to Japan, where it is widespread and often one of the dominant trees of Japan's cool-temperate deciduous forests, where it is often colocated with Quercus crispula (Japanese oak) and Acer mono (Painted maple). All three species function as canopy trees, with F. crenata being dominant. [24] [25] In parts of its range, other deciduous trees often found with F. crenata include: Fagus japonica , Magnolia obovata , Fraxinus lanuginosa , Acer japonicum , Quercus serrata , and Carpinus laxiflora . [26] [27]

Wind storms are the most significant cause of canopy damage to these forests. [25] [28] Shirakami-Sanchi is a UNESCO world heritage site in Aomori Prefecture and Akita Prefecture, Japan that features old-growth forests of F. crenata. The Shirakami-Sanchi forest is the largest remaining virgin beech forest in East Asia and the last virgin forest of F. crenata in Japan. [29] [30]

F. crenata is found from the Oshima Peninsula, including Okushiri Island, [6] in Hokkaidō and south to the Ōsumi Peninsula in Kyūshū. Th expansion of F. crenata from Honshu's northern Tōhoku region into Hokkaido began about 6,000 years BP. [6] In north-east Honshu it grows in large stands from sea level up to 1,400 meters (4,600 ft) but in the south-west of its range it is restricted to mountainous areas and occurs in small, isolated populations. It grows in well-drained, loamy or sandy soils. [24] F. japonica is mainly located on the Pacific side of Japan and is at lower elevations than F. crenata; though occassionally the two species are found together. [24] F. crenata grows in hardiness zones 4-7. [5] [31]

Ecology

F. crenata forest Fagus crenata in Mount Daimon 2011-06-19.jpg
F. crenata forest

Fagus crenata is not generally subject to serious diseases but can be attacked by aphids, wooly aphids, vine weevil, caterpillars, and spider mites. [5] The stag beetle Dorcus montivagus feeds exclusively on dead beech wood, almost always F. crenata. [32] Human disturbance combined with F. crenata's low mortality and high growth rate is enabling the species to spread further north in Hokkaido. [33] F. crenata has a low percentage of genetic inbreeding because of wind-pollination, self-incompatibility, and inbreeding depression. [34] Quercus crispula refoliates at a faster rate after insect defoliation than F. crenata. [35]

Reproduction in F. crenata significantly alters nitrogen uptake and allocation, with large amounts of nitrogen directed towards developing nuts, which reduces the amount of nitrogen available for new shoots and leaves. During masting years, the tree increases nitrogen uptake and uses existing nitrogen from other organs like cupules and senescing leaves to support nut ripening. The variation in nut production between masting and non-masting years varies several hundred-fold. [36]

Climate change is causing a reduction in the size of F. crenata forests. [37] Tropospheric ozone (O3) is phytotoxic to forests and has a detrimental effect on F. crenata, resulting in increased leaf senescence, sluggish stomatal response, decreased photosynthetic rate. [38] [39] [40] Budburst timing is strongly linked to temperature, late spring frosts, and heat. Genetic differentiation caused by this results in different phenological responses to climate, whereby northern populations have earlier budbursts because their response to these conditions cause genetic alterations in F. crenata. [41] [42] [43]

Dasyscyphella longistipitata is a fungus that is symbiotic with and grows solely on F. crenata in its cupules. Consequently, its distribution and northward expansion after the last Pleistocene era are identical. It plays a key role as a decomposer of woody debris. [44]

Cultivation

Fagus crenata bonsai Japanese Beech (Fagus Crenata) (3505588432).jpg
Fagus crenata bonsai

F. crenata prefers light or medium well-drained soil, including in chalky soils, clay, soil with high organic matter, and loam. [4] Preferred soils are less than 6.0 acid and above 8.0 alkaline. [4] It needs sun and is shade tolerant. While it does well in cold weather, it also needs hot summers. The trees grow very slowly. Because its roots can appear on the surface, there is often little or no vegetation under them. Seeds should be sown as soon as they are ripe in the autumn. Seedlings grow slowly the first few years and can be damaged by frosts. [45]

Uses

Ripe nuts, oil, and seeds can be eaten and the young, green leaves are cooked for food. Fagus crenata provides good wildlife cover, shade, and is used in bonsai . [5] [45] It is very popular in bonsai because it looks very similar to its fully grown forest specimens. [20] Being a dense hardwood, F. crenata is useful as firewood and in construction. [4]

See also

Notes

  1. ↑ Quercus crispula used to be known as Quercus mongolica (Japanese oak), var. grosseserrata. [3]
  2. ↑ The Global Biodiversity Information Facility recogizes Endlicher's article published in 1847 as the first use of this synonym. Kew Gardens recognizes Augustin Pyramus de Candolle's 1864 publication as the first usage. [15] [16]

References

  1. ↑ Botanic Gardens Conservation International (BGCI).; IUCN SSC Global Tree Specialist Group (2019). "Fagus crenata". IUCN Red List of Threatened Species . 2019 e.T138593394A143485665. doi: 10.2305/IUCN.UK.2019-1.RLTS.T138593394A143485665.en . Retrieved November 18, 2021.
  2. ↑ "Fagus ferruginea Aiton". Canadian Museum of Nature. Université de Montréal. Retrieved October 24, 2025.
  3. ↑ "Quercus mongolica Fisch". Trees and Shrubs Online. International Dendrology Society. Retrieved October 25, 2025.
  4. 1 2 3 4 5 6 7 "Fagus crenata". North Carolina Cooperative Extension. Retrieved October 23, 2025.
  5. 1 2 3 4 5 6 7 8 9 "Fagus crenata". Boone County Arboretum. Retrieved October 23, 2025.
  6. 1 2 3 4 Kiramura, Keiko; Matsui, Tetsuya; Kobayashi, Makoto; Namikawa, Kanji (December 15, 2022). "Possible northern persistence of Siebold's beech, Fagus crenata, at its northernmost distribution limit on an island in Japan Sea: Okushiri Island, Hokkaido". Frontiers in Plant Science. 13 990927. Bibcode:2022FrPS...1390927K. doi: 10.3389/fpls.2022.990927 . PMC   9797532 . PMID   36589061.
  7. ↑ "Fagus ferruginea Siebold". Global Biodiversity Information Facility. Retrieved October 24, 2025.
  8. ↑ "Universi Regni Japonici" [The Entire Japanese Kingdom]. Verhandelingen van het Bataviaasch Genootschap der Kunsten en Wetenschappen (Proceedings of the Batavian Society of Arts and Sciences) (in Latin). 12 (25). Biodiversity Heritage Library: 75-77 (foldout). 1830. Retrieved October 24, 2025.
  9. ↑ Akiyama, Shinobu; Thijsse, Gerard; Esser, Hans-Joachim; Ohba, Hideaki (December 2013). "Siebold and Zuccarini's Type Specimens and Original Materials from Japan, Part 2. Angiosperms. Dicotyledoneae 1". Journal of Japanese Botany. 86 (8): 350. Retrieved October 24, 2025.
  10. ↑ "Table of Contents (Back cover note)" (PDF). Arnoldia. Vol. 70, no. 4. Arnold Arboretum, Harvard University. 2013. p. 3. Retrieved October 25, 2025.
  11. ↑ von Siebold, Philipp Franz; Zuccarini, Joseph Gerhard (1835). Flora Japonica (in Latin). Vol. 1. Leiden: Lugduni Batavorum. pp. 1–596. Retrieved October 25, 2025.
  12. ↑ von Siebold, Philipp Franz; Zuccarini, Joseph Gerhard (1870). Flora Japonica (PDF) (in Latin). Vol. 2. Leiden: Lugduni Batavorum. pp. 1–150. Retrieved October 25, 2025.
  13. 1 2 3 "Fagus crenata Blume". Plants of the World Online. Kew Royal Botanic Gardens. Retrieved October 23, 2025.
  14. ↑ "Fagus grandifolia". Royal Horticultural Society. Retrieved October 25, 2025.
  15. 1 2 "Fagus sieboldii Endl. ex A.DC". Plants of the World Online. Kew Royal Botanic Gardens. Retrieved October 25, 2025.
  16. 1 2 "Fagus sieboldii Endl". Global Biodiversity Information Facility. Retrieved October 25, 2025.
  17. ↑ Denk, Thomas; Grimm, Guido W.; Cardoni, Simone; Csilléry, Katalin; Kurz, Mirjam; Schulze, Ernst-Detlef; Simeone, Marco Cosimo; Worth, James R. P. (2024). "A subgeneric classification of Fagus (Fagaceae) and revised taxonomy of western Eurasian beeches". Willdenowia. 54 (2–3): 151–181. Bibcode:2024Willd..5454301D. doi: 10.3372/wi.54.54301 . ISSN   0511-9618.
  18. ↑ Cardoni, Simone; Piredda, Roberta; Denk, Thomas; Grimm, Guido W.; Papageorgiou, Aristotelis C.; Schulze, Ernst-Detlef; Scoppola, Anna; Shanjani, Parvin Salehi; Suyama, Yoshihisa (October 19, 2021). "5S-IGS rDNA in wind-pollinated trees (Fagus L.) encapsulates 55 million years of reticulate evolution and hybrid origins of modern species". The Plant Journal. 109 (4): 909–926. bioRxiv   10.1101/2021.02.26.433057 . doi:10.1111/tpj.15601. PMC   9299691 . PMID   34808015 . Retrieved October 24, 2024.
  19. ↑ Denk, Thomas; Grimm, Guido W.; Hemleben, Vera (June 2005). "Patterns of molecular and morphological differentiation in Fagus (Fagaceae): phylogenetic implications". American Journal of Botany. 92 (6): 1006–1016. doi:10.3732/ajb.92.6.1006. ISSN   0002-9122. PMID   21652485.
  20. 1 2 Hodge, W. H. (1972). "Japanese Bonsai and Bonsai Shows". Arnoldia. 32 (5): 247. doi:10.5962/p.389393. JSTOR   42953902.
  21. ↑ Berry, Edward W. (March 1916). "Notes on the Ancestry of the Beech". The Plant World. 19 (3): 66–67. JSTOR   43477503.
  22. ↑ Beekes, Robert (2010). Etymological Dictionary of Greek. Leiden and Boston: Brill. pp. 1565–1566. ISBN   978-9004174184 . Retrieved October 23, 2025.
  23. ↑ "Eucalyptus crenulata". New Zealand Plant Conservation Network. Retrieved October 23, 2025.
  24. 1 2 3 Okaura, T.; Harada, K. (2002). "Phylogeographical structure revealed by chloroplast DNA variation in Japanese Beech (Fagus crenata Blume)" (PDF). Heredity. 88 (4). Nature Publishing Group: 322–329. Bibcode:2002Hered..88..322O. doi: 10.1038/sj.hdy.6800048 . PMID   11920142 . Retrieved October 23, 2025.
  25. 1 2 Cao, K. F.; Ohkubo, T. (1999). "Suppression and Release during Canopy Recruitment in Fagus Crenata and Acer Mono in Two Old-Growth Beech Forests in Japan". Plant Ecology. 145 (2): 281–290. Bibcode:1999PlEco.145..281C. doi:10.1023/A:1009888128269. JSTOR   20050863.
  26. ↑ Homma, Kohsuke (1997). "Effects of Snow Pressure on Growth Form and Life History of Tree Species in Japanese Beech Forest". Journal of Vegetation Science. 8 (6): 782–783. JSTOR   3237022.
  27. ↑ Nagamatsu, Dai; Seiwa, Kenji; Sakai, Akiko (2002). "Seedling Establishment of Deciduous Trees in Various Topographic Positions". Journal of Vegetation Science. 13 (1): 35–44. JSTOR   3236651.
  28. ↑ Yamashita, Asuka; et al. (2002). "Impact of a Strong Typhoon on the Structure and Dynamics of an Old-Growth Beech (Fagus crenata) Forest, Southwestern Japan". Folia Geobotanica. 37 (1): 5–16. Bibcode:2002FolGe..37....5Y. doi:10.1007/BF02803187. JSTOR   25133873.
  29. ↑ "Shirakami-Sanchi". UNESCO World Heritage Centre. United Nations. 1992–2018. Retrieved January 6, 2018.
  30. ↑ "Shirakami-sanchi". International Union for Conservation of Nature and UN Environment World Conservation Monitoring Centre. 2017. Retrieved October 3, 2025.
  31. ↑ "Fagus crenata". North Carolina State University. Archived from the original on October 9, 2007. Retrieved October 23, 2025.
  32. ↑ Ueki, Gaku; Tojo, Koji (February 2023). "The phylogeography of the stag beetle Dorcus montivagus (Coleoptera, Lucanidae): Comparison with the phylogeography of its specific host tree, the Japanese beech Fagus crenata". Entomological Science. 26 (1) e12535. doi:10.1111/ens.12535.
  33. ↑ Aiba, Shin-Ichiro; Namikawa, Kanji; Matsui, Tetsuya; Abo, Eri (October 2022). "Stand dynamics over 15 years including an outlying population of Fagus crenata at the northern margin of its distribution range in Hokkaido, Japan". Ecological Research. 38 (6): 740–752. doi:10.1111/1440-1703.12367.
  34. ↑ Inanaga, Michiko; et al. (November 2014). "Distance-dependent but genetically random mating in a Japanese beech (Fagus crenata) population". Botany. 92 (11): 795–803. Bibcode:2014Botan..92..795I. doi:10.1139/cjb-2014-0024.
  35. ↑ {Nakajima, Haruki (2018). "Refoliation of Deciduous Canopy Trees Following Severe Insect Defoliation: Comparison of Fagus crenata and Quercus crispula". Plant Ecology. 219 (6): 665–675. JSTOR   48725133.
  36. ↑ Han, Qingmin; Kabeya, Daisuke; Inagaki, Yoshiyuki (October 2017). "Influence of reproduction on nitrogen uptake and allocation to new organs in Fagus crenata". Tree Physiology. 37 (10): 1436–1443. doi:10.1093/treephys/tpx095. PMID   28985424.
  37. ↑ Endoh, Keith; et al. (December 2017). "Cryopreservation of Fagus crenata seeds: estimation of optimum moisture content for maintenance of seed viability by Bayesian modeling". Canadian Journal of Forest Research. 48 (2): 192–196. doi:10.1139/cjfr-2017-0286.
  38. ↑ Hoshika, Yasutomo; Watanabe, Makoto; Inada, Naoki; Takayoshi, Koike (July 2012). "Ozone-induced stomatal sluggishness develops progressively in Siebold's beech (Fagus crenata)". Environmental Pollution. 166: 152–156. Bibcode:2012EPoll.166..152H. doi:10.1016/j.envpol.2012.03.013. PMID   22504428.
  39. ↑ Ariura, Ryo; et al. (September 2023). "Effects of elevated ozone and carbon dioxide on the dynamic photosynthesis of Fagus crenata seedlings under variable light conditions". Science of the Total Environment. 891 164398. Bibcode:2023ScTEn.89164398A. doi:10.1016/j.scitotenv.2023.164398. PMID   37244616.
  40. ↑ Watanabe, Makoto; et al. (2018). "Mesophyll conductance to CO2 in leaves of Siebold's beech (Fagus crenata) seedlings under elevated ozone". Journal of Plant Research. Physiological Ecology of Woody Species in Response to Air Pollution and Climate Changes. 131 (6): 907–914. doi:10.1007/s10265-018-1063-4. PMID   30203164.
  41. ↑ Osada, Noriyuki; et al. (September 2018). "Genetic differentiation in the timing of budburst in Fagus crenata in relation to temperature and photoperiod". International Journal of Biometeorology. 62 (9): 1763–1776. Bibcode:2018IJBm...62.1763O. doi:10.1007/s00484-018-1579-2. PMID   29978264.
  42. ↑ Sugimoto, Saki; Ishida, Kiyoshi (2023). "Genetic Differentiation of Budburst Timing in Fagus crenata Populations along a Spatial Gradient in Late Frost Timing in the Hakkoda Mountains, Northern Japan". Forests. 14 (4) 659. Bibcode:2023Fore...14..659S. doi: 10.3390/f14040659 .
  43. ↑ Kon, Hirokazu; Noda, Takashi; Terazawa, Kazuhiko; Yasaka, Michiyasu; Koyama, Hiromasa (January 2006). "Proximate factors causing mast seeding in Fagus crenata: the effects of resource level and weather cues". Canadian Journal of Botany. doi:10.1139/b05-120.
  44. ↑ Gasca-Pineda, Jaime; Velez, Patricia; Hosoya, -Tsuyoshi (2020). "Phylogeography of post-Pleistocene population expansion in Dasyscyphella longistipitata (Leotiomycetes, Helotiales), an endemic fungal symbiont of Fagus crenata in Japan". MycoKeys (65): 1–24. doi: 10.3897/mycokeys.65.48409 . PMC   7086340 . PMID   32218686.
  45. 1 2 "Fagus crenata - Blume". Plants for a Future. Retrieved October 23, 2025.

Further reading

This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.