Hymenoscyphus fraxineus | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Fungi |
Division: | Ascomycota |
Class: | Leotiomycetes |
Order: | Helotiales |
Family: | Helotiaceae |
Genus: | Hymenoscyphus |
Species: | H. fraxineus |
Binomial name | |
Hymenoscyphus fraxineus Baral et al. (2014) [1] | |
Synonyms | |
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Hymenoscyphus fraxineus is an ascomycete fungus that causes ash dieback, a chronic fungal disease of ash trees in Europe characterised by leaf loss and crown dieback in infected trees. The fungus was first scientifically described in 2006 under the name Chalara fraxinea. Four years later it was discovered that Chalara fraxinea is the asexual (anamorphic) stage of a fungus that was subsequently named Hymenoscyphus pseudoalbidus and then renamed as Hymenoscyphus fraxineus.
It is now believed that the trees reported to have died in Poland in 1992 weren infected with this pathogen. It is now widespread in Europe, with up to 85% mortality rates recorded in plantations and 69% in woodlands. [2] It is closely related to a native fungus Hymenoscyphus albidus , which is harmless to European ash trees. [3] [4] A 2016 report published in the Journal of Ecology posited that a combination of H. fraxineus and emerald ash borer attacks could result in the extinction of European ash trees. [5]
The fungus Hymenoscyphus fraxineus was first identified and described in 2006 under the name Chalara fraxinea. [6] In 2009, based on morphological and DNA sequence comparisons, Chalara fraxinea was suggested to be the asexual stage (anamorph) of the ascomycete fungus Hymenoscyphus albidus . [6] However, Hymenoscyphus albidus has been known from Europe since 1851 and is not regarded as pathogenic. [7] In 2010, through molecular genetic methods, the sexual stage (teleomorph) of the fungus was recognized as a new species and named Hymenoscyphus pseudoalbidus. [6] Four years later it was determined that "under the rules for the naming of fungi with pleomorphic life-cycles", the correct name should be Hymenoscyphus fraxineus. [1] Hymenoscyphus fraxineus is "morphologically virtually identical" to Hymenoscyphus albidus, but there are notable genetic differences between the two species. [8]
The lifecycle of Hymenoscyphus fraxineus comprises two phases: sexual and asexual. [9] The asexual stage (anamorph) grows in affected trees attacking the bark and encircling twigs and branches. [9] The sexual, reproductive stage, (teleomorph) grows during summer on ash petioles in the previous year's fallen leaves. [7] The ascospores are produced in asci and are transmitted by wind, which may explain the rapid spread of the fungus. [7] The origins of the disease are uncertain, [10] but researchers are investigating the theory that the fungus originated in Asia, where ash trees are immune to the disease. [11] Genetic analysis of the fungus Lambertella albida which grows harmlessly on petioles of the Manchurian ash ( Fraxinus mandschurica ) in Japan, has shown that it is likely to be the same species as Hymenoscyphus fraxineus. [12]
In December 2012, teams from The Sainsbury Laboratory (TSL) and the John Innes Centre in Norwich sequenced the genome of the fungus in December 2012. The sequence has been published on the website OpenAshDieBack and offers insights into the mechanisms of infection in trees by the fungus. The study has identified toxin genes and other genes that may be responsible for the virulence of the fungus. In the long term researchers aim to find the genes that confer resistance to the pathogen in some ash trees. [13]
Trees now believed to have been infected with this pathogen were reported dying in large numbers in Poland in 1992. [14] By the mid 1990s, the fungus had also been identified in Lithuania, Latvia and Estonia. [15] However, it was not until 2006 that the fungus's asexual stage, Chalara fraxinea, was first described by scientists, and 2010 before its sexual stage was described. [14] By 2008, the disease had also been discovered in Scandinavia, the Czech Republic, Slovenia, Germany, Austria and Switzerland. [16] By 2012, it had spread to Belgium, France, Hungary, Italy, Luxembourg, [17] the Netherlands, Romania, Russia, Britain and Ireland. [18] [19] By 2016, it was already identified in central Norway, the northernmost distribution area of the ash tree. [20]
Up to 85% mortality rates due to H. fraxineus have been recorded in plantations and 69% in woodlands. [2] The disease has caused a large-scale decline of ash trees across Poland, [21] with evidence suggesting that in the long term "15 to 20 per cent of trees may survive without exhibiting symptoms." [22] In 2012, it was reported that the disease was reaching its peak in Sweden and Denmark, and that it was entering a post-decline (or chronic) phase in Latvia and Lithuania. [10] The disease was first observed in Denmark in 2002, and had spread throughout the country by 2005. [23] In 2009 it was estimated that 50 per cent of Denmark's ash trees were affected by crown dieback, [23] and a 2010 estimate stated that 60–90% of ash trees in Denmark were affected and may eventually disappear. [24] The disease was first reported in Sweden in 2003. [25] A survey conducted in Götaland in 2009 found that more than 50% of the trees had noticeable thinning and 25% were severely injured. [25]
A Danish study found that substantial genetic variation between ash trees affected their level of susceptibility. [26] However, the proportion of trees with a high level of natural resistance seemed to be very low, probably less than 5%. [26] A Lithuanian trial based on the planting of trees derived from both Lithuanian and foreign populations of European ash found 10% of trees survived in all progeny trials to the age of eight years. [27]
So far the fungus has mainly affected the European ash ( Fraxinus excelsior ) and its cultivars, but it is also known to attack the narrow-leafed ash ( Fraxinus angustifolia ). [28] The manna ash ( Fraxinus ornus ) is also a known host, although it is less susceptible than the other European ash species. [28] Experiments in Estonia have shown that several North American ash species are susceptible, especially the black ash ( Fraxinus nigra ), and to a lesser extent the green ash ( Fraxinus pennsylvanica ). [28] The white ash ( Fraxinus americana ) and the Asian species known as Manchurian ash ( Fraxinus mandschurica ) showed only minor symptoms in the study. [28]
Initially, small necrotic spots (without exudate) appear on stems and branches. These necrotic lesions then enlarge in stretched, perennial cankers on the branches, wilting, premature shedding of leaves and particularly in the death of the top of the crown. [29] Below the bark, necrotic lesions frequently extend to the xylem, especially in the axial and paratracheal ray tissue. [30] The mycelium can pass through the simple pits, perforating the middle lamella but damage to either the plasmalemma or cell walls was not observed. [31] The disease is often chronic but can be lethal. [18] It is particularly destructive of young ash plants, killing them within one growing season of symptoms becoming visible. [32] Older trees can survive initial attacks, but tend to succumb eventually after several seasons of infection. [32]
There are currently no effective strategies for managing the disease, and most countries which have tried to control its spread have failed. [11] The removal of trees in infected areas has little effect as the fungus lives and grows on leaf litter on the forest floor. [11] Research at the Swedish University of Agricultural Sciences suggests that the deliberate destruction of trees in an infected area can be counterproductive as it destroys the few resistant trees alongside the dying ones. [33] One approach to managing the disease may be to take branches from resistant trees and graft them to rootstock to produce seeds of resistant trees in a controlled environment. [33] A Lithuanian trial searching for disease-resistance resulted in the selection of fifty disease-resistant trees for the establishment of breeding populations of European ash in different provinces of Lithuania. [27] A breeding programme for resistant trees is a viable strategy [34] but the process of restoring the ash tree population across Europe with resistant trees is likely to take decades. [33]
The fungus was first detected in Britain during February 2012 at sites that had received saplings from nurseries in the preceding five years. [14] A ban on imports of ash from other European countries was imposed in October 2012 after infected trees were found in established woodland. [35] On 29 October Environment minister David Heath confirmed that 100,000 nursery trees and saplings had been deliberately destroyed. [11] [36] The government also banned ash imports but experts described their efforts as "too little too late". [37] The UK Government Emergency Committee COBR convened on 2 November to address the crisis. [38] A survey of Scottish trees started in November 2012. [39] A 2020 study suggested that certain landscapes with hedgerows and woods made up of different types of tree resisted the disease better than areas mainly populated with ash trees. [40]
The Forestry Commission has produced guidance [41] and requested people report [42] possible cases.
Comparisons have been made to the outbreak of Dutch elm disease in the 1960s and 1970s. [43] In 2012 it was estimated that up to 99% of the 90 million ash trees in the UK would be killed by the disease. [44]
On 9 November 2012 the United Kingdom Government unveiled its strategy. Environment Secretary Owen Paterson announced that it was acknowledged that the disease was here to stay in the UK and that the focus would be on slowing its spread. Young and newly planted trees with the disease would be destroyed; however, mature trees would not be removed because of the implications for wildlife that depends on the trees for their natural habitat. The strategy unveiled by Paterson included:
In March 2013 Owen Paterson announced that the United Kingdom Government would plant a quarter of a million ash trees in an attempt to find strains that are resistant to the fungus. [46]
In February 2016 the BBC program "Countryfile" presented a case study of enhanced resistance to ash dieback following soil treatment by injecting enriched "Biochar" - a type of charcoal. Over a three-year period, twenty trees had remained free of disease despite a severe infestation of the surrounding trees. [47] [48]
In December 2016, writing in Nature, [49] Dr Richard Buggs reported that the common ash (Fraxinus excelsior) had been genetically sequenced for the first time and UK specimens appeared more resistant than Danish ones. [50]
In August 2018 Defra and the Forestry Commission announced that at Westonbirt Arboretum the fungus had been found infecting three new hosts: Phillyrea (mock privet), Phillyrea angustifolia (narrow-leaved mock privet) and Chionanthus virginicus (white fringetree). [51] [52] These were the first findings on hosts other than Fraxinus anywhere in the world. [53] All three new hosts are in the same taxonomic family as ash, the Oleaceae. [51] The trees were all in the vicinity of infected European ash. [53] In response to the findings on the new hosts, Nicola Spence, the UK Chief Plant Health Office, said that, "Landscapers, gardeners and tree practitioners should be vigilant for signs of ash dieback on these new host species, and report suspicious findings through Tree Alert". [52]
In June 2019, Defra published a report summarising the current state of knowledge of ash dieback, and priority areas for future research. [54] In 2019 and 2020, the UK government and Future Trees Trust planted 3,000 ash trees in Hampshire to establish the Ash Archive. All the trees came from shoots of trees that demonstrated resistance to the fungus. The Ash Archive will form the basis of a breeding program. [55]
On 12 October 2012 the Department of Agriculture, Food and the Marine confirmed the first recorded instance of the fungus in Ireland, at a plantation in County Leitrim. [56] Legislation was introduced in both Northern Ireland and the Republic of Ireland on 26 October banning the importation and movement of ash plants from infected parts of Europe. [56] By 23 September 2013, a survey conducted by the Irish Government revealed that the disease had been identified at ninety-six sites across the Republic of Ireland. [57] As of August 2021, Teagasc warns that: "The disease is now prevalent throughout most of the island of Ireland and is likely to cause the death of the majority of the ash trees over the next two decades." [58]
The first cases in Northern Ireland were confirmed at five sites in counties Down and Antrim on 16 November 2012. [59] By 4 December 2012 the disease had been confirmed at sixteen sites in counties Down, Antrim, Tyrone and Londonderry. [60]
Due to the importance of F. excelsior as a host, Jönsson and Thor 2012 find that H. fraxineus is subjecting rare/threatened lichens to an unusually high (0.38) coextinction risk probability vis-a-vis the host tree in the wooded meadows of Gotland, Sweden. [61] Studies detected no signs of ash mortality compensation by the surviving trees, particularly in mixed forests, indicating a mid-term habitat loss and niche replacement of ash. [20]
Fraxinus, commonly called ash, is a genus of plants in the olive and lilac family, Oleaceae, and comprises 45–65 species of usually medium-to-large trees, most of which are deciduous trees, although some subtropical species are evergreen trees. The genus is widespread throughout much of Europe, Asia, and North America.
The pathogenic fungus Cryphonectria parasitica is a member of the Ascomycota. This necrotrophic fungus is native to East Asia and South East Asia and was introduced into Europe and North America in the early 1900s. The fungus spread rapidly and caused significant tree loss in both regions.
Fraxinus americana, the white ash or American ash, is a fast-growing species of ash tree native to eastern and central North America.
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.
The emerald ash borer, also known by the acronym EAB, is a green buprestid or jewel beetle native to north-eastern Asia that feeds on ash species. Females lay eggs in bark crevices on ash trees, and larvae feed underneath the bark of ash trees to emerge as adults in one to two years. In its native range, it is typically found at low densities and does not cause significant damage to trees native to the area. Outside its native range, it is an invasive species and is highly destructive to ash trees native to Europe and North America. Before it was found in North America, very little was known about emerald ash borer in its native range; this has resulted in much of the research on its biology being focused in North America. Local governments in North America are attempting to control it by monitoring its spread, diversifying tree species, and through the use of insecticides and biological control.
Phytophthora cinnamomi, also known as cinnamon fungus, is a soil-borne water mould that produces an infection which causes a condition in plants variously called "dieback", "root rot", or, "ink disease".
Fraxinus pennsylvanica, the green ash or red ash, is a species of ash native to eastern and central North America, from Nova Scotia west to southeastern Alberta and eastern Colorado, south to northern Florida, and southwest to Oklahoma and eastern Texas. It has spread and become naturalized in much of the western United States and also in Europe from Spain to Russia.
Dieback may refer to a number of plant problems and diseases including:
Cronartium ribicola is a species of rust fungus in the family Cronartiaceae that causes the disease white pine blister rust. Other names include: Rouille vésiculeuse du pin blanc (French), white pine Blasenrost (German), moho ampolla del pino blanco (Spanish).
Forest dieback is a condition in trees or woody plants in which peripheral parts are killed, either by pathogens, parasites or conditions like acid rain, drought, and more. These episodes can have disastrous consequences such as reduced resiliency of the ecosystem, disappearing important symbiotic relationships and thresholds. Some tipping points for major climate change forecast in the next century are directly related to forest diebacks.
Forest pathology is the research of both biotic and abiotic maladies affecting the health of a forest ecosystem, primarily fungal pathogens and their insect vectors. It is a subfield of forestry and plant pathology.
Armillaria root rot is a fungal root rot caused by several different members of the genus Armillaria. The symptoms are variable depending on the host infected, ranging from stunted leaves to chlorotic needles and dieback of twigs and branches. However, all infected hosts display symptoms characteristic of being infected by a white rotting fungus. The most effective ways of management focus on limiting the spread of the fungus, planting resistant species, and removing infected material. This disease poses a threat to the lumber industry as well as affecting recreational areas.
Arger Fen is a 49.7-hectare (123-acre) biological Site of Special Scientific Interest (SSSI) south-east of Sudbury in Suffolk, England. The site occupies two separate areas. The 17.6-hectare (43-acre) Arger Fen Local Nature Reserve is part of the larger eastern block, and contains part of the 21-hectare (52-acre) Tiger Hill Local Nature Reserve, along with part of the 110-hectare (270-acre) Arger Fen and Spouse's Vale, a nature reserve managed by the Suffolk Wildlife Trust. The site lies in the Dedham Vale Area of Outstanding Natural Beauty,
Hymenoscyphus albidus is a saprotrophic fungus which grows on the dead leaves of ash trees.
The Future Trees Trust is a charity that aims to improve and increase the stock of hardwood trees in Britain and Ireland.
CandidatusPhytoplasma fraxini is a species of phytoplasma, a specialized group of bacteria which lack a cell wall and attack the phloem of plants. This phytoplasma causes the diseases ash yellows and lilac witches' broom.
Anne Edwards is a British plant scientist, based at the John Innes Centre and was the first person in the UK to identify Ash dieback disease in England,
The Ash Archive is a project founded in 2019 to restore ash trees to the landscape in England. English ash trees experienced massive dieback beginning in 2012 as a result of a fungal pathogen, Hymenoscyphus fraxineus. The archive contains over 3,000 trees, all of which propagated from the shoots of trees that had demonstrated some resistance to the fungus. The archive was established with £1.9 million in government funding, and followed a five-year project to identify ash trees that were resistant to the fungus. One of the final trees in the archive was planted in January 2020 by Nicola Spence, the Chief Plant Health Officer of the UK government. Spence said, "I'm delighted to acknowledge the successes of the Ash Archive project and welcome the International Year of Plant Health by planting an ash dieback-tolerant tree."
Lejeunea mandonii, also known as Atlantic lejeunea is a species of liverwort from the Lejeuneaceae family.
Fraxinus paxiana is a species of flowering plant in the family Oleaceae, native to central and southern China. A tree reaching 20 m (66 ft), it is found in forested valley slopes, usually from 400 to 1,100 m above sea level. In the wild it is heavily infected with Hymenoscyphus fraxineus, the fungal pathogen that causes ash dieback, but shows little damage.