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Biology

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The ash flowers in April and May (2). The male flowers do not release pollen until after the styles of the female flowers belonging to the same tree have ceased to be receptive; this helps to avoid self-fertilisation (3). Ashes grow at an extremely fast rate until 50 years of age; after this point they cease to increase in height. They first begin to produce flowers and seeds after they reach 30 years of age (3). Ash wood is valued for its fast growth, strength and elasticity; it has been put to a wide range of uses and is still used to make hockey sticks, billiard cues and oars, as well as walking sticks, for its ability to withstand shock. The ancient technique of coppicing extends the life of the tree; in Suffolk a coppiced ash is estimated to be at least 1,000 years old (5). Scandinavian mythology holds that the ash was the 'tree of life'; it was believed to have healing powers in Britain, and was widely regarded as a source of magic and mystery. Unfortunately, the mysterious aura of the ash has declined in modern times; it is now commonly viewed as a 'weed tree' due to its rapid colonisation of new areas and fast growth (5).
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Conservation

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As this species is common and widespread, conservation action is not necessary.
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Description

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The ash is one of our tallest native trees. It has a fairly open crown, becoming oval or spherical in shape as it ages (3). The bark is greyish in colour and smooth, becoming fissured as it grows old. This tree is easy to identify in winter by the black buds, which occur in pairs (4). The tiny purple flowers appear before the leaves and occur in male and female clusters (4), they do not have petals or sepals (3). Ash is one of the last trees to produce leaves in spring; the compound leaves are pinnate, with 7-13 toothed oval-shaped leaflets (4). The elongate, winged fruits hang in clusters, they are initially green in colour, but eventually become brown (3).
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Habitat

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The ash develops its impressive crown when it grows in damp soil rich in minerals. Main habitats include riverbanks, meadow and valley woodlands, and deciduous woodlands (3).
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Range

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The ash is common throughout Britain and most of the rest of Europe (2).
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Status

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Widespread and common (2).
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Threats

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This tree is not threatened.
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Associations

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Plant / associate
Abdera biflexuosa is associated with Fraxinus excelsior

Foodplant / gall
Aceria fraxinivora causes gall of inflorescence of Fraxinus excelsior

Plant / associate
Anisoxya fuscula is associated with Fraxinus excelsior

Plant / associate
Anthocoris gallarum-ulmi is associated with aphid-galled leaf of Fraxinus excelsior

Plant / associate
Anthocoris simulans is associated with Fraxinus excelsior
Other: major host/prey

In Great Britain and/or Ireland:
Foodplant / pathogen
Armillaria mellea s.l. infects and damages Fraxinus excelsior

Foodplant / miner
larva of Aulagromyza heringii mines leaf of Fraxinus excelsior
Other: sole host/prey

Foodplant / saprobe
fruitbody of Auricularia auricula-judae is saprobic on wood of Fraxinus excelsior
Other: minor host/prey

Plant / associate
Biphyllus lunatus is associated with dead branch of Fraxinus excelsior

Foodplant / feeds on
Botryodiplodia coelomycetous anamorph of Botryodiplodia fraxini feeds on Fraxinus excelsior

Foodplant / saprobe
fruitbody of Callistosporium luteo-olivaceum is saprobic on dead wood of Fraxinus excelsior
Remarks: Other: uncertain

Foodplant / saprobe
immersed, gregarious perithecium of Ceriospora caudae-suis is saprobic on submerged, decorticate branch (small) of Fraxinus excelsior

Foodplant / sap sucker
Chionaspis salicis sucks sap of live stem of Fraxinus excelsior

Plant / associate
Corticeus bicolor is associated with Fraxinus excelsior

Foodplant / internal feeder
caterpillar of Cossus cossus feeds within live trunk of Fraxinus excelsior

Foodplant / saprobe
scattered, immersed, minute, pallid, mostly unilocular stroma of Cytosporina coelomycetous anamorph of Cytosporina millepunctata is saprobic on dead, fallen branch of Fraxinus excelsior
Remarks: season: 11

Foodplant / gall
larva of Dasineura acrophila causes gall of leaf of Fraxinus excelsior

Foodplant / gall
larva of Dasineura fraxinea causes gall of leaf of Fraxinus excelsior

Foodplant / gall
larva of Dasineura fraxini causes gall of leaf of Fraxinus excelsior

Foodplant / saprobe
scattered, erumpent pycnidium of Phomopsis coelomycetous anamorph of Diaporthe samaricola is saprobic on fallen samara (seed end) of Fraxinus excelsior
Remarks: season: 10-5

Foodplant / saprobe
often clustered conidioma of Phomopsis coelomycetous anamorph of Diaporthe scobina is saprobic on dead petiole of Fraxinus excelsior
Remarks: season: 3-9

Foodplant / internal feeder
larva of Dorcus parallelipipedus feeds within dead or rotten wood of Fraxinus excelsior
Other: major host/prey

Foodplant / internal feeder
larva of Dryocoetinus alni feeds within cambium of Fraxinus excelsior

Foodplant / internal feeder
larva of Dryocoetinus villosus feeds within cambium of Fraxinus excelsior

Foodplant / saprobe
fruitbody of Henningsomyces candidus is saprobic on decayed wood of Fraxinus excelsior

Foodplant / pathogen
fruitbody of Heterobasidion annosum infects and damages live root of Fraxinus excelsior

Foodplant / internal feeder
larva of Hylastes opacus feeds within cambium of Fraxinus excelsior
Other: minor host/prey

Foodplant / internal feeder
larva of Hylesinus crenatus feeds within cambium of Fraxinus excelsior

Foodplant / internal feeder
larva of Hylesinus oleiperda feeds within cambium of Fraxinus excelsior

Foodplant / saprobe
fruitbody of Inonotus hispidus is saprobic on dead trunk of Fraxinus excelsior
Other: major host/prey

Foodplant / internal feeder
larva of Leperisinus orni feeds within cambium of Fraxinus excelsior

Foodplant / internal feeder
larva of Leperisinus varius feeds within cambium of Fraxinus excelsior

Foodplant / internal feeder
larva of Limoniscus violaceus feeds within wood of Fraxinus excelsior

Plant / associate
Lytta vesicatoria is associated with Fraxinus excelsior

Foodplant / saprobe
gregarious pycnidium of Macrophoma coelomycetous anamorph of Macrophoma fraxini is saprobic on dead, fallen twig of Fraxinus excelsior
Remarks: season: 2-5

Foodplant / open feeder
nocturnal larva of Macrophya punctumalbum grazes on leaf of Fraxinus excelsior
Other: major host/prey

Plant / associate
mycelial muff of tree of Morchella esculenta is associated with live root of Fraxinus excelsior
Other: major host/prey

Foodplant / spot causer
hypophyllous, minute, numerous, aggregated, semi-immersed, black pycnidium of Septoria coelomycetous anamorph of Mycosphaerella fraxini causes spots on live leaf of Fraxinus excelsior

Foodplant / sap sucker
Orthotylus nassatus sucks sap of Fraxinus excelsior
Other: minor host/prey

Plant / associate
nymph of Orthotylus tenellus is associated with Fraxinus excelsior
Other: major host/prey

Plant / associate
Paromalus flavicornis is associated with under bark of Fraxinus excelsior

Foodplant / saprobe
resupinate fruitbody of Peniophora cinerea is saprobic on dead wood of Fraxinus excelsior
Other: major host/prey

Plant / associate
Phloiotrya vaudoueri is associated with Fraxinus excelsior

Foodplant / parasite
Phyllactinia fraxini parasitises live leaf of Fraxinus excelsior

Foodplant / parasite
hypophyllous Phyllactinia guttata parasitises live leaf of Fraxinus excelsior

Foodplant / spot causer
pycnidium of Phyllosticta coelomycetous anamorph of Phyllosticta fraxinicola causes spots on live leaf of Fraxinus excelsior
Remarks: season: 7-9

Foodplant / internal feeder
larva of Platypus cylindrus feeds within wood of Fraxinus excelsior

Plant / associate
Platyrhinus resinosus is associated with Fraxinus excelsior

Foodplant / internal feeder
larva of Prionychus ater feeds within decaying wood of Fraxinus excelsior

Foodplant / gall
Prociphilus bumeliae causes gall of leaf (petiole) of Fraxinus excelsior

Foodplant / sap sucker
nymph of Psallus flavellus sucks sap of Fraxinus excelsior

Foodplant / sap sucker
nymph of Psallus lepidus sucks sap of Fraxinus excelsior

Foodplant / feeds on
Pseudoloxops coccineus feeds on Fraxinus excelsior

Foodplant / gall
Pseudomonas syringae ssp savastanoi pv. fraxini causes gall of live, cankered trunk of Fraxinus excelsior

Foodplant / gall
Psyllopsis fraxini causes gall of leaf of Fraxinus excelsior

Foodplant / feeds on
Ptelobius vittatus feeds on Fraxinus excelsior

Foodplant / internal feeder
larva of Rhagium mordax feeds within rotting stump (cambium and outer sapwood) of Fraxinus excelsior

Foodplant / internal feeder
larva of Sinodendron cylindricum feeds within dead or rotten wood of Fraxinus excelsior

Foodplant / internal feeder
underground larva of Stenocorus meridianus feeds within dead root of Fraxinus excelsior

Foodplant / internal feeder
larva of Tetrops starkii feeds within dead branch of Fraxinus excelsior

Foodplant / open feeder
larva of Tomostethus nigritus grazes on leaf of Fraxinus excelsior

Plant / epiphyte
colony of Trentepohlia abietina grows on bark of Fraxinus excelsior

Foodplant / saprobe
immersed, stromatic, in group of 3 to 8 perithecium of Valsa cypri is saprobic on dead branch (cortex) of Fraxinus excelsior

Foodplant / gall
Vasates epiphyllus causes gall of leaf of Fraxinus excelsior

Foodplant / gall
Vasates fraxini causes gall of leaf of Fraxinus excelsior

Foodplant / hemiparasite
haustorium of Viscum album is hemiparasitic on branch of Fraxinus excelsior

Foodplant / internal feeder
caterpillar of Zeuzera pyrina feeds within live bud of Fraxinus excelsior

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Fraxinus excelsior

provided by wikipedia EN

Fraxinus excelsior, known as the ash, or European ash or common ash to distinguish it from other types of ash, is a flowering plant species in the olive family Oleaceae. It is native throughout mainland Europe[2] east to the Caucasus and Alborz mountains, and Great Britain and Ireland, the latter determining its western boundary. The northernmost location is in the Trondheimsfjord region of Norway.[3][4] The species is widely cultivated and reportedly naturalised in New Zealand and in scattered locales in the United States and Canada.[5][6][7]

Description

Male flowers
Seeds of Fraxinus excelsior, popularly known as "keys" or "helicopter seeds", are a type of fruit known as a samara

It is a large deciduous tree growing to 12–18 m (39–59 ft) (exceptionally to 43 m or 141 ft) tall with a trunk up to 2 m (6.6 ft) (exceptionally to 3.5 m or 11 ft) diameter, with a tall, narrow crown.[2] The bark is smooth and pale grey on young trees, becoming thick and vertically fissured on old trees. The shoots are stout, greenish-grey, with jet-black buds (which distinguish it from most other ash species, which have grey or brown buds). The leaves are opposite, 20–35 cm (7.9–13.8 in) long, pinnately compound, with 7–13 leaflets with coarsely serrated margins, elliptic to narrowly elliptic, 3–12 cm (1.2–4.7 in) long and 0.8–3 cm (0.31–1.18 in) broad and sessile on the leaf rachis.[2] There are no stipules.[2] These features distinguish ash from mountain ash (Sorbus aucuparia) in which the leaves are alternate with paired stipules. The leaves are often among the last to open in spring, and the first to fall in autumn if an early frost strikes; they often fall dull green or develop a bright yellow autumn colour. The flowers are borne in short panicles, open before the leaves, and have no perianth. The female flowers are somewhat longer than the male flowers, dark purple, without petals, and are wind-pollinated. Both male and female flowers can occur on the same tree, but it is more common to find all male and all female trees. A tree that is all male one year can produce female flowers the next, and similarly a female tree can become male. The fruit is a samara 2.5–4.5 cm (0.98–1.77 in) long and 5–8 mm (0.20–0.31 in) broad, often hanging in bunches through the winter;[8] they are often called 'ash keys'.[3][9][10] If the fruit is gathered and planted when it is still green and not fully ripe, it will germinate straight away, however once the fruit is brown and fully ripe, it will not germinate until 18 months after sowing (i.e. not until two winters have passed).[11]

European ash rarely exceeds 250 years of age. However, there are numerous specimens estimated between 200 and 250 years old and there are a few over 250. The largest is in Clapton Court, England and is 9 m (29.5 ft) in girth. There are several examples over 4.5 metres (14.8 ft) in Derbyshire alone.

Distribution

Fraxinus excelsior is native to Europe from northern Spain to Russia, and from southern Fennoscandia to northern Greece.[2] It is also considered native in southwestern Asia from northern Turkey east to the Caucasus and Alborz mountains. The northernmost location is in the Trondheimsfjord region of Norway.[3][4] The species is widely cultivated and reportedly naturalized in New Zealand and in scattered locales in the United States and Canada including Nova Scotia, New Brunswick, Quebec, Massachusetts, Connecticut, New York, New Jersey, Maryland, Ontario, Ohio, Kentucky and British Columbia.

It is native throughout Britain and Ireland, particularly on limestone, as in northern Scotland, where the most northerly native ashwood in Britain occurs on limestone at Rassal Ashwood.[12] It is widely planted elsewhere.[13]

Ecology

Ash tree (~20m tall) in Wales at 185 m asl in July (l) and March (r), showing branch structure

Ash occurs on a wide range of soil types, but is particularly associated with basic soils on calcareous substrates. The most northerly ashwood in Britain is on limestone at Rassal, Wester Ross, latitude 57.4278 N.[14] Ash prefers moister soil types and is commonly limited by temperature and so not found at the higher colder altitudes in much of Europe, though in Iran, it may reach 2000 m asl. As a young seedling, it is shade tolerant, but older trees are light-demanding. It is an early-succession species and may well outcompete beech and oak, which are later-succession species.[15]

F. excelsior mycorrhizae are of the internal arbuscular mycorrhizal type, in which the fungus grows within the tissues of the root and forms branched, tree-like structures within the cells of the root cortex. Unlike other Fraxinus species, F. excelsior does not form ectomycorrhizae.[2]

The Biological Records Centre of the UK records 111 species of insects and mites using ash as a food plant, of which 29 are specific to ash. A further six are specific to ash and its Oleaceae relative wild privet (Ligustrum vulgare).[16] A number of Lepidoptera species use the species as a food source.[17] One example of an ash-specific feeding moth is the centre-barred sallow (Atethmia centrago). The larvae burrow into the buds when newly hatched and later feed on the flowers and leaves.[18] A common moth which causes the browning of ash leaves, as well as garden privet and lilac, is Gracillaria syringella. The usually gregarious larvae form an epidermal gallery (i.e. feed within the leaf) which leads to a brown blotch with black frass. Later, two successive cones are formed by folding the tip of a leaf downwards.[19]

In Britain, 14 galls have been recorded on ash. The British Plant Gall Society defines a gall as "... an abnormal growth produced by a plant under the influence of another organism".[20]

Ash dieback

Ash dieback is caused by the fungus Hymenoscyphus fraxineus which was previously known as Chalara fraxinea. Research into the genetics of the resistance of ash (Fraxinus excelsior) has shown that resistance does occur in European populations, but at least for the samples tested, it is neither common nor strong.[21][22][23][24] Due to the importance of F. excelsior as a host, Jönsson and Thor 2012 find that rare/threatened lichens face an unusually high (0.38) coextinction risk probability vis-a-vis the host tree in the wooded meadows of Gotland, Sweden.[25]

Genome

The genome of Fraxinus excelsior is being sequenced by two groups of scientists in the United Kingdom. A group at Queen Mary University of London led by Richard Buggs are sequencing the self-pollinated offspring of a tree from Worcestershire, held by the Earth Trust.[26] A group at the John Innes Centre and The Genome Analysis Centre led by Allan Downie are sequencing "Tree 35" from Denmark, discovered by Erik Kjær, which has survived 8 years of ash dieback.[27]

Uses

Veneer of common ash wood
Replica of the body frame from the Volvo ÖV 4 car, made primarily from ash wood

The resilience and rapid growth made it an important resource for smallholders and farmers. It was probably the most versatile wood in the countryside with wide-ranging uses. Until World War II, the trees were often coppiced on a 10-year cycle to provide a sustainable source of timber for fuel and poles for building and woodworking.[28] The colour of the wood ranges from creamy white to light brown, and the heart wood may be a darker olive-brown. Ash timber is hard, tough and very hard-wearing, with a coarse, open grain and a density of 710 kg/m3.[29] It lacks oak's natural resistance to decay, and is not as suitable for posts buried in the ground. Because of its high flexibility, shock resistance, and resistance to splitting, ash wood is the traditional material for bows, tool handles, especially for hammers and axes, tennis rackets, and snooker cue sticks,[30] and it was extensively used in the construction of early aircraft. Ash was commonly used green for making chair frames which would be seated with another timber or with woven rush (e.g. those made by Philip Clissett, see also The English Regional Chair[31]). The parts were turned on a pole lathe or shaped with a drawknife. The practice essentially died out in the early 20th century, but has seen a revival in recent years.

Ash is an important constituent of wood pasture, a European management system in which open woodland provided shelter and forage for grazing animals.[12] Ash was coppiced and pollarded, often in hedgerows, and evidence in the form of some huge boles with multiple trunks emerging at head height can still be seen in parts of Britain. The Glen Lyon ash is a notable example of a pollarded ash which at about 400–500 years of age achieved a girth of 6 m.[12] In Northumberland, crab and lobster pots (traps) sometimes known as 'creeves' by local people are still made from ash sticks. Because of its elasticity European ash wood was commonly used for walking sticks. Poles were cut from a coppice and the ends heated in steam. The wood could then be bent in a curved vise to form the handle of the walking stick. The light colour and attractive grain of ash wood make it popular in modern furniture such as chairs, dining tables, doors, and other architectural features and wood flooring.

Ash is the only wood used for the manufacture of hurleys, referred to as hurls in parts of Leinster and known as a camán in Irish, the timber sticks used in the game of hurling in Ireland. Hurleys are manufactured from the butt log (bottom 1.5-m of the stem) and from trees ideally of a diameter at breast height around 25–30 cm. Only fast-grown, straight, and knot-free ash can be used for this purpose. Due to the lack of available ash in Ireland, over 75% of the timber needed to produce the 350,000 hurleys required for the game annually must be imported, mostly from Eastern European countries.[32] The importance of ash timber to the game of hurling is reflected in the fact that the game is referred to all over Ireland as "The Clash of the Ash".

Ash is valuable as firewood because it burns well even when 'green' (freshly cut).[33] Ash bark and leaves are used in modern herbal medicine for its astringent and laxative properties.[34]

Mythology

In the 13th-century Edda and other writing relating to Norse mythology, the vast ash tree Yggdrasil ("the steed (gallows) of Odin"), watered by three magical springs, serves as axis mundi, sustaining the nine worlds of the cosmos in its roots and branches.[35]

Folklore

On the Isle of Bute in Scotland, lovers reportedly used to eat leaves of an ash tree known as the "Dreamin' Tree" that grew near the church of St Blane, and the pleasant dreams they then experienced revealed their actual spouses and intended fates.[36]

Cultivars

Ash saplings from a mast year

Its many cultivars include;

  • Fraxinus excelsior 'Aurea', the traditional, slow-growing golden ash ─ not to be confused with 'Jaspidea'
  • Fraxinus excelsior 'Aurea Pendula' (weeping golden ash)
  • Fraxinus excelsior 'Autumn Blaze'
  • Fraxinus excelsior 'Autumn Purple'
  • Fraxinus excelsior 'Crispa'
  • Fraxinus excelsior 'Diversifolia' (one-leaved ash)
  • Fraxinus excelsior 'Erosa'
  • Fraxinus excelsior 'Jaspidea' a modern, vigorous golden ash
  • Fraxinus excelsior 'Monophylla'
  • Fraxinus excelsior 'Nana'
  • Fraxinus excelsior 'Pendula' (weeping ash), one of the best-known cultivars, widely planted during the Victorian era, grows vigorously forming an attractive small to medium-sized tree with mounds of weeping branches
  • Fraxinus excelsior 'Skyline'

Gallery

References

  1. ^ Khela, S.; Oldfield, S. (2018). "Fraxinus excelsior". IUCN Red List of Threatened Species. 2018: e.T203367A67807718. doi:10.2305/IUCN.UK.2018-1.RLTS.T203367A67807718.en. Retrieved 12 November 2021.
  2. ^ a b c d e f Thomas, Peter A. (2016). "Biological Flora of the British Isles: Fraxinus excelsior". Journal of Ecology. 104 (4): 1158–1209. doi:10.1111/1365-2745.12566. S2CID 86930831.
  3. ^ a b c Rushforth, K. (1999). Trees of Britain and Europe. Collins ISBN 0-00-220013-9.
  4. ^ a b Den virtuella floran: Fraxinus excelsior distribution
  5. ^ Kew World Checklist of Selected Plant Families, Fraxinus excelsior
  6. ^ Biota of North America Program, Fraxinus excelsior
  7. ^ Altervista Flora of the United States and Canada, Fraxinus excelsior
  8. ^ Kilbracken, J.1983. Larousse Easy way guide Trees. Larousse. ISBN 0-7523-0027 X
  9. ^ Mitchell, A. F. (1974). A Field Guide to the Trees of Britain and Northern Europe. Collins ISBN 0-00-212035-6
  10. ^ Mitchell, A. F. (1982). The Trees of Britain and Northern Europe. Collins ISBN 0-00-219037-0
  11. ^ Edlin, H. L. (1985). Broadleaves. Forestry Commission booklet 20. HMSO. p. 36. ISBN 9780117100398.
  12. ^ a b c Stiven, Roland; Holl, Kate (2004). Wood Pasture. Perth, UK: Scottish Natural Heritage. ISBN 978-1853973864.
  13. ^ "Online atlas of the British and Irish Flora, Fraxinus excelsior (Ash)". Biological Records Centre and Botanical Society of Britain and Ireland.
  14. ^ "Wood Pasture: Rassal Ashwood National Nature Reserve". Scottish Natural Heritage.
  15. ^ Dorota Dobrowolska; Sebastian Hein; Anne Oosterbaan; Sven Wagner; Jo Clark; Jens Peter Skovsgaard (April 2011). "A review of European ash (Fraxinus excelsior L.): implications for silviculture Forestry". Forestry: An International Journal of Forest Research. 84 (2): 133–148. doi:10.1093/forestry/cpr001.
  16. ^ Rackham, Oliver (2014). The Ash Tree. Toller Fratrum, Dorset: Little Toller Books. pp. 25–6. ISBN 978-1-908213-14-3.
  17. ^ Alan Stubbs. "Invertebrates associated with Ash" (PDF). Archived from the original (PDF) on 3 September 2013. Retrieved 28 February 2015.
  18. ^ "Centre-barred Sallow Atethmia centrago". UKmoths. Retrieved 28 July 2017.
  19. ^ "15.014 Gracillaria syringella (Fabricius, 1794)". British leafminers. Retrieved 28 July 2017.
  20. ^ Redfern, Margaret; Shirley, Peter; Bloxham, Michael (2011). British Plant Galls (Second ed.). Shrewsbury: FSC Publications. ISBN 978-1-85153-284-1.
  21. ^ Stener LG (2012). "Clonal differences in susceptibility to the dieback of Fraxinus excelsior in southern Sweden". Scandinavian Journal of Forest Research. 28 (3): 205–216. doi:10.1080/02827581.2012.735699. S2CID 85292870.
  22. ^ Kjær ED, et al. (2012). "Adaptive potential of ash (Fraxinus excelsior) populations against the novel emerging pathogen Hymenoscyphus pseudoalbidus". Evolutionary Applications. 5 (3): 219–228. doi:10.1111/j.1752-4571.2011.00222.x. PMC 3353348. PMID 25568043.
  23. ^ McKinney LV, et al. (2011). "Presence of natural genetic resistance in Fraxinus excelsior (Oleraceae) to Chalara fraxinea (Ascomycota): an emerging infectious disease". Heredity. 106 (5): 788–797. doi:10.1038/hdy.2010.119. PMC 3186218. PMID 20823903.
  24. ^ Pliūra A, Lygis V, Suchockas V, Bartkevičius E (2011). "Performance of twenty four European Fraxinus excelsior populations in three Lithuanian progeny trials with a special emphasis on resistance to Chlara fraxinea". Baltic Forestry. 17 (1): 17–34.
  25. ^ Oliva, Jonàs; Redondo, Miguel Ángel; Stenlid, Jan (25 August 2020). "Functional Ecology of Forest Disease". Annual Review of Phytopathology. Annual Reviews. 58 (1): 343–361. doi:10.1146/annurev-phyto-080417-050028. ISSN 0066-4286. PMID 32396761. S2CID 218618105.
  26. ^ "Welcome to Ash tree genomes - Ash Tree Genomes". www.ashgenome.org.
  27. ^ Heap, Tom (16 June 2013). "Ash genome reveals fungus resistance". BBC News.
  28. ^ Mabey, R. (1996). Flora Britannica. Sinclair-Stevenson Ltd ISBN 1-85619-377-2.
  29. ^ "Ash". Niche Timbers. Retrieved 19 August 2009.
  30. ^ Petrică Tudor M, Ingrid Agnes M, Szilard B. 2011. Study of Physical Characteristics, Mechanical and Technological Properties of Wood Species from the Fraxinus Genus Encountered in Romania Compared to Other Main Forestry Species. Natural Resources and Sustainable Development [1].
  31. ^ Cotton, Bernard D. (1990). The English Regional Chair. Woodbridge, Suffolk: Antiques Collectors Club. ISBN 1-85149-023-X.
  32. ^ John Whiriskey; Paul McCarthy, eds. (May 2006). Ash For Hurleys (PDF) (Report). Fact Sheet No. 35. Teagasc - The Agriculture and Food Development Authority. Archived from the original (PDF) on 22 November 2007.
  33. ^ "The burning properties of wood" (PDF). The Scout Association. 1999. Archived from the original (PDF) on 23 December 2012. Retrieved 1 November 2010.
  34. ^ Pliûra, A.; Heuertz, M. (2003). Common ash – Fraxinus excelsior: Technical guidelines for genetic conservation and use (PDF) (Report). EUFORGEN.
  35. ^ Simek, Rudolf (2007). Dictionary of Northern Mythology. Translated by Angela Hall. D.S. Brewer. ISBN 978-0-85991-513-7.
  36. ^ Downie, R. Angus (1934). Bute and the Cumbraes Glasgow & London: Blackwood & Son Ltd. p. 83

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Fraxinus excelsior: Brief Summary

provided by wikipedia EN

Fraxinus excelsior, known as the ash, or European ash or common ash to distinguish it from other types of ash, is a flowering plant species in the olive family Oleaceae. It is native throughout mainland Europe east to the Caucasus and Alborz mountains, and Great Britain and Ireland, the latter determining its western boundary. The northernmost location is in the Trondheimsfjord region of Norway. The species is widely cultivated and reportedly naturalised in New Zealand and in scattered locales in the United States and Canada.

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