Oak wilt | |
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Causal agents | Bretziella fagacearum |
Hosts | Quercus spp. |
Vectors | Nitidulidae |
EPPO code | CERAFA |
Distribution | US |
Symptoms | leaf discoloration, wilt, defoliation and death |
Bretziella fagacearum | |
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Spores produced by the oak wilt fungus (a) Endoconidia (b) Conidiophore | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Fungi |
Division: | Ascomycota |
Class: | Sordariomycetes |
Order: | Microascales |
Family: | Ceratocystidaceae |
Genus: | Bretziella |
Species: | B. fagacearum |
Binomial name | |
Bretziella fagacearum (Bretz) Z.W. de Beer, Marincowitz, T.A. Duong & M.J. Wingfield [1] | |
USA counties with oak wilt (2017) | |
Synonyms | |
Oak wilt is a fungal disease caused by the organism Bretziella fagacearum that threatens Quercus spp. [3] The disease is limited to the eastern half of the United States; first described in the 1940s in the Upper Mississippi River Valley. The pathogen penetrates xylem tissue, preventing water transport and causing disease symptoms. [5] Symptoms generally consist of leaf discoloration, wilt, defoliation, and death. The disease is dispersed by insect vectors and to adjacent trees through underground root networks. However, human spread is the most consequential dispersal method. [6] Moving firewood long distances can potentially transport diseases and invasive species.
Oak wilt is a devastating exotic disease, killing some trees rapidly in a single season. [7] Oak wilt is an important disease in urban areas where trees are highly valued. The disease reduces property values because of the loss of trees and is economically costly to the property owner since they or the local government must pay for tree removal. Additionally, preventing the spread of the disease to healthy trees is costly and requires vigilance. Oak wilt is also an important disease in a forest setting, as entire forest stands can die within a few years. [8] There is a narrow window to salvage diseased trees for hardwood lumber and often the disease is not discovered within that logging window. [9] The ecological impacts to forests is also a concern. The disease is currently restricted to North America, but is potentially a serious threat to oaks worldwide. [10]
All Quercus spp. appear susceptible to the disease, with 33 oak species confirmed to be susceptible; including three species of Castanea , one species of Castanopsis , one species of Lithocarpus , and some oaks native to Europe (Q. petraea, Q. pubescens, & Q. robur). [11] [12] Generally, red oaks (subsection Lobatae) display more severe symptoms with rapid and frequent mortality (particularly Q. velutina, Q. rubra, Q. ellipsoidalis & Q. coccinea). White oaks (subsection Quercus) develop symptoms more slowly, rarely die, and can recover from the pathogen with damage limited to a few branches (particularly Q. alba, & Q. macrocarpa). Live oaks (Q. fusiformis & Q. virginiana) display intermediate symptoms compared to red or white oaks. However, live oaks are semi-evergreen, can propagate vegetatively by root suckering, and cohabitate with other live oaks in dense stands enabling interconnected root systems. These traits are favorable for local spread of the disease in an oak-grassland savanna. [13]
Oak wilt is one of three devastating North American vascular wilt diseases that appeared in the early 20th century. The other two vascular wilts are chestnut blight (1900–1950) and Dutch elm disease (1928–1980). Each of these diseases have depopulated their respective host tree populations. Chestnut trees were the dominant overstory tree species before chestnut blight and elms were an iconic landscape tree that bordered streets before Dutch elm disease. Oak wilt and the newly emerging emerald ash borer have the potential to devastate other important North American tree species with large geographical and cultural significance. Range expansion of oak wilt to the Western United States (or to other continents) is a major concern.
The asexual stage of oak wilt was first described in 1942 in Wisconsin. [14] [15] Soon thereafter the disease was reported throughout the Upper Midwest and Central forests. The early 20th Century coincided with oak regeneration after significant logging in the Mid-Atlantic and Great Lakes region. Deforestation and fire suppression in this region altered the ecology to favor oak–hickory forests, instead of coniferous forests and grasslands. [16] [17] [18] Subsequently, the host for the disease became more prevalent and promoted oak wilt infections. Moving timber during the late 19th Century and early 20th Century, in the period of railroad expansion, coincides with the discovery of the oak wilt disease in the United States.
The origin of the disease is unknown, but probably emerged from Mexico, Central America, or South America. [19] Mexico is the global center of oak diversity, supporting it as the endemic range of oak wilt. [20] [21] Any biocontrol or disease resistance for this pathogen will likely come from Mexico. The disease currently affects much of the eastern and central US, from northern New York to Central Texas. [22] It is particularly common in the Midwest where conditions are usually favorable for spore production and beetle activity during spring and early summer. Oak wilt is a major problem in Illinois, Iowa, Michigan, Minnesota, Texas, and Wisconsin. [23] [24] [25]
The fungus overwinters on dead tissue from diseased trees. Symptoms first appear in spring and summer. Highly susceptible species typically die within one year (often within six weeks) after symptoms appear. Symptoms begin in the tops of trees and can be difficult to notice. The disease progresses inward and downward from the tree top. Leaves become chlorotic beginning at the leaf tip and leaf edges. An abrupt demarcation of chlorotic veins and green tissue is often a distinguishing characteristic in live oak infections. [26] The foliage may droop, curl lengthwise, wilt, and begin to fall. Leaves drop from the tree in the middle of summer, however less susceptible trees may retain leaves longer and resemble seasonal autumn foliage. Highly susceptible species will exhibit rapid crown dieback, while less susceptible species may only lose a few scattered branches. Live oaks may survive several years with progressive dieback, but often die within six months. Following defoliation, fungal fruiting bodies develop from mycelium under the bark of the tree. The mats grow to 10 – 20 cm in size, elliptical in shape, and grey in color with white margins that darken with age. These mats are not found on live oaks and rarely on white oaks. Trees capable of producing mats are called potential spore-producing trees (PSPT). Brown streaks in the sapwood is also observed in the oak wilt disease. However, this symptom is not always associated with the disease.
The oak wilt fungus can spread from diseased trees to healthy trees in several ways. The disease can spread long distances (overland) by airborne spores in open wounds caused by wind damage, pruning, or other mechanical damage. Alternatively, under ideal conditions (temperature, moisture content, wood pH) spore mats form under the bark of the dead tree. Spore mats develop in the spring or fall for 2–3 weeks. The center of spore mats produce chains of barrel shaped spores, called endoconidia. Conidia are asexual spores dispersed by air, rain, and insects. [27] If compatible mating types are present, these mats will also produce sexual spores called ascospores in fruiting structures called perithecia. Ascospores are spread by water and insects. [27] These spore mats (or pressure pads) increase in size, eventually breaking through the bark and releasing a fruity odor that attracts wildlife, including sap beetles, bark beetles, other insects, birds and animals, such as squirrels. Insect vectors transmit the disease in spring to early summer in the Mid-West and late Winter in Texas. Insect transmission is the primary way new infection foci originate.
The fungus can spread short distances through naturally occurring root grafts. Root grafts form when two or more underground roots merge from adjacent trees. Typically, roots from the same, or similar species, can form root grafts as their cambia are pressed together and combine. [28] [29] Fungal spores in the xylem travel to nearby trees through these root grafts and can rapidly kill many trees simultaneously. This transmission method accounts for the vast majority of infections and is particularly devastating as groups of trees are killed. The disease can extend 10 – 20m per year (40m per year in Texas) from the infection foci to surrounding trees. Diseased trees can continue to harbor and transmit the disease for several years through the root network.
The disease results from fungal spores clogging xylem vessels and preventing water and nutrient flow. Mycelia growth between and through vessels end up blocking xylem pits in the vessel endwalls. Tylose protrusion and the accumulation of 'gums' will further obstruct vessels. Tylose is an outgrowth of parenchyma cells created as a plant defense against pathogens, water deficiency, wounding, and heartwood formation. Tylose formation signals senescence of adjacent parenchyma cells and secretion of secondary metabolites (called gums), which may include phenolics. [30] The interruption of the xylem vessels precedes tylose formation. Tylose and secreted gums act as a barrier to slow the colonization of the pathogen and play an important part in plant defenses. However, the action to compartmentalize the oak wilt fungus ultimately obstructs all water conductance, leading to death. The fungus can survive in the xylem for multiple years, if the tree is not killed.
Early detection and prompt action are essential for successful management of oak wilt. The specific measures taken depend on several circumstances but should include appropriate combinations of the following:
- Prevent New Infections
- Remove and dispose of oak wilt-infected red oaks immediately.
- Avoid wounding oak trees, including pruning from,
- February through June in Texas.
- April through October in the Mid-West.
- Sterilize/sanitize all pruning equipment between trees.
- Paint all wounds and fresh stumps immediately regardless of season.
- Handle oak firewood cautiously, burn all firewood before spring, and never store unseasoned oak wood from infected trees near healthy oaks.
- Cover unseasoned firewood (from infection centers and unknown origins) with clear plastic and bury the edges of the plastic.
- Diversify Your Landscape
- Plant trees that are native and/or adapted to your area.
- Favor a diversity of tree species.
- Avoid wounding oaks during planting.
- Stop Spread through Root Connections
- Install a trench at least 4 ft deep and 100 ft beyond the perimeter of infection centers (last symptomatic tree) to break up root connections.
- Cut or uproot all trees within the 100-ft barrier (except those injected with fungicide).
- Inject High-Value Oaks with Fungicide
- Identify susceptible, high-value oak trees in proximity to expanding oak wilt infection centers.
- Consult a trained and licensed arborist (with certified applicator's license) for treatment of susceptible trees with injections of propiconazole.
Elimination of the disease is not possible; therefore, managing the disease is essential to prevent economic and ecological losses.[ citation needed ] Management of the oak wilt disease includes forest integrated pest management; such as sanitation, chemical application, and cultural control. Ideally, several methods are used in conjunction to enhance disease control. Any chosen method relies on specific landowner objectives; such as protecting high value trees, treating individual trees, halting or slowing the spread of an infection center, and reducing the number of new infection foci. All methods depend on timely detection and accurate diagnosis of the disease to be beneficial. Aerial observation (or remote sensing) is able to identify infected forest stands by observing the dead crowns of trees in summer. The use of spectroscopy is being developed for large scale detection and monitoring of oak wilt. [31]
Chemical control can be preventative or therapeutic, depending on risk and resources available. Propiconazole is the principle fungicide for treatment against oak wilt. Propiconazole is a broad-spectrum systemic fungicide that interferes with the biosynthesis of ergosterol in cell membranes by binding to 14 alpha-demethylase. Tree injection is the preferred application method to deliver targeted control. Tree injections involve intravascular injections with positive pressure to force the chemical throughout the vascular system of the tree. This method is relatively expensive and requires a trained arborist to perform . [32] [33] Propiconazole injection does not offer protection to neighboring trees and must be applied to all target trees.
Preventative propiconazole application does not prevent infection, rather it delays symptoms and reduces mortality. All oak species studied have benefited from preventative propiconazole treatment. [11] This method is often applied to high value trees in an urban area, specifically Northern red oaks and live oaks. White oaks are more disease resistant, thus preventative treatment is unnecessary. Likewise, therapeutic propiconazole application does not eradicate the fungal infection, rather it delays symptoms and reduces mortality. Highly susceptible red oaks rarely benefit from therapeutic treatment, but symptomatic white oaks improve with treatment. Asymptomatic live oaks will respond better to propiconazole treatment than symptomatic trees.
Spring application is the most effective time for chemical treatment. Multiple applications, every two years, may be necessary for long-term disease control.
Mechanical separation of the underground root connections will not allow the disease to transfer to adjacent trees. However, ensuring all root connections are severed is difficult and impractical to verify. Notwithstanding, digging a trench (or plowline) four feet deep around infected trees is an effective cultural control strategy. The plowline should encompass any infected tree. In practice this consists of all trees expected to be connected by a root graft with an infected tree, in addition to all symptomatic trees. In the Mid-West, a plowline 50 feet away from infected trees is recommended. In Central Texas, live oak lateral roots grow at a shallow depth in rocky soil, allowing an extensive root network with neighboring trees. For this reason, a plowline 100 feet away from infected trees is recommended. [13] A second plowline between all symptomatic trees and visibly healthy trees will reinforce this control strategy.
The plowline can be created with agricultural machinery, such as an excavator, rock saw, vibratory plow, and bulldozer with ripper or subsoiler. Equipment costs and availability will vary.
The placement of a root barrier can offer additional protection to trenching, but increases total costs. A geomembrane is a semipermeable textile (similar to landscape fabric) that physically blocks roots from coming into contact. It is essential that trenching and geomembrane installation occur before removing infected trees.
Sanitation entails removing infectious material to reduce inoculum before new infections can develop. Red oaks are the only group capable of forming spore mats, designated as PSPTs. Therefore, removing any PSPTs that become infected is essential to minimize new infection foci. Furthermore, removing all PSPTs, regardless of symptoms, within an infected area reinforces the process. In practice this consists of removing all PSPTs within the plowline (see Mechanical). Trees will need to be removed annually to sustain control over the years. Tree removal involves felling and burying or burning the logs, ensuring all inoculum is discarded. Alternatively, logs and slash can be chipped or mulched on site. Tree stumps can also be removed to increase sanitation.
Girdling infected trees is another method to reduce the spread of oak wilt; although, not as effective as whole tree removal. Girdling requires the complete detachment of the cambium from the PSPTs. Moreover, debarking the trunk of the tree (up to 4 feet) is essential. Oak wilt does not produce fruiting bodies on dead or dry wood. Debarking speeds the drying process and assists Hypoxylon coccineum in colonizing the wood.
Sap beetles are opportunistic insects, incapable of penetrating a tree without an open wound. Therefore, avoid pruning or felling oak trees when fungal spores and beetles are active. In the Mid-West avoid injuring oaks from April to October and prune limbs after the first hard frost, or from November until April. In Texas avoid pruning oaks from February through June. Moreover, clean pruning equipment between each tree and apply tree paint to any injury or open wound. Injuries often occur during construction and severe weather.
Silviculture involves keeping a forest healthy. Typically, a healthy forest with healthy trees will be more resistant to pests and diseases. Thinning is the process of removing unwanted trees to promote the growth of the desired trees. Oaks are shade intolerant species. Releasing (or thinning) oaks from competition provides more light, moisture, and nutrients to the remaining oaks. Overall the oaks become stronger, more healthy, and more capable to resist pests and disease.
Increasing tree species diversity (i.e. species evenness) in a forest is another method to lessen the impact of the disease. Evidence shows increasing diversity in a landscape can increase forest resilience to pests and disease. [34] [35] [36] [37] Moreover, increasing diversity can increase soil microbial communities and ecosystem services. [38] [39] [40] [41] [42]
Education is the most valuable tool to combat the spread of pests and diseases. In this context, warning the public about the spread of oak wilt by humans. Specifically, people take fuelwood from one location to another location, often long distances. This action is responsible for moving pathogens in those logs to places they are not currently present. Spreading oak wilt to new locations through firewood is a major problem. Moreover, covering firewood with clear plastic can solarize the wood pile and eradicate any pathogens.
Prevent the spread of invasive species and diseases
- Don't take firewood with you on your camping trip, RV adventure, or to your hunting camp.
- Don't bring firewood back from your second home to your place in the suburbs.
- Buy firewood near where you will burn it, or gather firewood on site when permitted.
- A good rule of thumb is only using wood that was cut within 50 miles of where you'll have your fire.
- Certified heat-treated firewood is safe to move long distances.
- Aged or seasoned wood is still not safe.
- Just because it is dry doesn't mean that bugs can't crawl onto it- and some insects can take several years to mature inside the wood.
- Wood that looks clean and healthy can still have tiny insect eggs, or microscopic fungi spores, that will start a new and deadly infestation.
Texas root rot is a disease that is fairly common in Mexico and the southwestern United States resulting in sudden wilt and death of affected plants, usually during the warmer months. It is caused by a soil-borne fungus named Phymatotrichopsis omnivora that attacks the roots of susceptible plants. It was first discovered in 1888 by Pammel and later named by Duggar in 1916.
Fusarium wilt is a common vascular wilt fungal disease, exhibiting symptoms similar to Verticillium wilt. This disease has been investigated extensively since the early years of this century. The pathogen that causes Fusarium wilt is Fusarium oxysporum. The species is further divided into formae speciales based on host plant.
Verticillium is a genus of fungi in the division Ascomycota, and are an anamorphic form of the family Plectosphaerellaceae. The genus used to include diverse groups comprising saprobes and parasites of higher plants, insects, nematodes, mollusc eggs, and other fungi, thus the genus used to have a wide-ranging group of taxa characterised by simple but ill-defined characters. The genus, currently thought to contain 51 species, may be broadly divided into three ecologically based groups - mycopathogens, entomopathogens, and plant pathogens and related saprotrophs. However, the genus has undergone recent revision into which most entomopathogenic and mycopathogenic isolates fall into a new group called Lecanicillium.
Diplodia tip blight, also known as Sphaeropsis blight, is a widespread disease affecting conifers caused by an opportunistic fungal pathogen, Diplodia sapinea. It is found in “both hemispheres between the latitudes 30° and 50° north and south". The diseases symptoms include: damping off and collar rot of seedlings, stem canker, root disease, and, most commonly, shoot blight. These symptoms have caused significant economic loss to nurseries and pine plantations. In a nursery in the north-central United States, losses of 35% have been reported. Shoot blight and eventual die back can cause a reduction of marketable volume in timber by 63%. Infection of terminal shoots can result in dead-top which significantly limits the usable length of the tree trunk. The presence of the pathogen in concert with severe weather conditions can lead to extreme loss. Following a severe hailstorm in South Africa, nearly 5,000 acres of pine plantation were infected with Diplodia tip blight. It was necessary to prematurely harvest large swaths of the plantations resulting in a loss of 45%. Areas that were not harvested prematurely still suffered an average timber loss of 11%.
Xylella fastidiosa is an aerobic, Gram-negative bacterium of the genus Xylella. It is a plant pathogen, that grows in the water transport tissues of plants and is transmitted exclusively by xylem sap-feeding insects such as sharpshooters and spittlebugs. Many plant diseases are due to infections of X. fastidiosa, including bacterial leaf scorch, oleander leaf scorch, coffee leaf scorch (CLS), alfalfa dwarf, phony peach disease, and the economically important Pierce's disease of grapes (PD), olive quick decline syndrome (OQDS), and citrus variegated chlorosis (CVC). While the largest outbreaks of X. fastidiosa–related diseases have occurred in the Americas and Europe, this pathogen has also been found in Taiwan, Israel, and a few other countries worldwide.
Verticillium wilt is a wilt disease affecting over 350 species of eudicot plants. It is caused by six species of Verticillium fungi: V. dahliae, V. albo-atrum, V. longisporum, V. nubilum, V. theobromae and V. tricorpus. Many economically important plants are susceptible including cotton, tomatoes, potatoes, oilseed rape, eggplants, peppers and ornamentals, as well as others in natural vegetation communities. Many eudicot species and cultivars are resistant to the disease and all monocots, gymnosperms and ferns are immune.
Ophiostoma ulmi is a species of fungus in the family Ophiostomataceae. It is one of the causative agents of Dutch elm disease. It was first described under the name Graphium ulmi, and later transferred to the genus Ophiostoma.
Ralstonia solanacearum is an aerobic non-spore-forming, Gram-negative, plant pathogenic bacterium. R. solanacearum is soil-borne and motile with a polar flagellar tuft. It colonises the xylem, causing bacterial wilt in a very wide range of potential host plants. It is known as Granville wilt when it occurs in tobacco. Bacterial wilts of tomato, pepper, eggplant, and Irish potato caused by R. solanacearum were among the first diseases that Erwin Frink Smith proved to be caused by a bacterial pathogen. Because of its devastating lethality, R. solanacearum is now one of the more intensively studied phytopathogenic bacteria, and bacterial wilt of tomato is a model system for investigating mechanisms of pathogenesis. Ralstonia was until recently classified as Pseudomonas, with similarity in most aspects, except that it does not produce fluorescent pigment like Pseudomonas. The genomes from different strains vary from 5.5 Mb up to 6 Mb, roughly being 3.5 Mb of a chromosome and 2 Mb of a megaplasmid. While the strain GMI1000 was one of the first phytopathogenic bacteria to have its genome completed, the strain UY031 was the first R. solanacearum to have its methylome reported. Within the R. solanacearum species complex, the four major monophyletic clusters of strains are termed phylotypes, that are geographically distinct: phylotypes I-IV are found in Asia, the Americas, Africa, and Oceania, respectively.
Brenneria salicis is a Gram-negative bacterium that is pathogenic on plants.
Ceratocystis fimbriata is a fungus and a plant pathogen, attacking such diverse plants as the sweet potato and the tapping panels of the Para rubber tree. It is a diverse species that attacks a wide variety of annual and perennial plants. There are several host-specialized strains, some of which, such as Ceratocystis platani that attacks plane trees, are now described as distinct species.
Nectria cinnabarina, also known as coral spot, is a plant pathogen that causes cankers on broadleaf trees. This disease is polycyclic and infects trees in the cool temperate regions of the Northern Hemisphere. N. cinnabarina is typically saprophytic, but will act as a weak parasite if presented with an opportunity via wounds in the tree or other stressors that weaken the tree's defense to the disease. A study published in 2011 showed that this complex consists of at least 4 distinct species. There are only a few ways to manage this disease with techniques such as sanitation and pruning away branches that have the cankers. N. cinnabarina is not as significant a problem as other Nectria spp., some of which are the most important pathogens to infect hardwood trees.
Ophiostoma novo-ulmi is a species of fungus in the family Ophiostomataceae. It is one of the key causative agents associated with Dutch Elm Disease (DED), along with Ophiostoma ulmi and Ophiostoma himal-ulmi.
Verticillium dahliae is a fungal plant pathogen. It causes verticillium wilt in many plant species, causing leaves to curl and discolor. It may cause death in some plants. Over 400 plant species are affected by Verticillium complex.
Laminated root rot also known as yellow ring rot is caused by the fungal pathogen Phellinus weirii. Laminated root rot is one of the most damaging root disease amongst conifers in northwestern America and true firs, Douglas fir, Mountain hemlock, and Western hemlock are highly susceptible to infection with P. weirii. A few species of plants such as Western white pine and Lodgepole pine are tolerant to the pathogen while Ponderosa pine is resistant to it. Only hardwoods are known to be immune to the pathogen.
Phytophthora kernoviae is a plant pathogen that mainly infects European beech and Rhododendron ponticum. It was first identified in 2003 in Cornwall, UK when scientists were surveying for the presence of Phytophthora ramorum. This made it the third new Phytophthora species to be found in the UK in a decade. It was named Phytophthora kernoviae after the ancient name for Cornwall, Kernow. It causes large stem lesions on beech and necrosis of stems and leaves of Rhododendron ponticum. It is self-fertile. It has also been isolated from Quercus robur and Liriodendron tulipifera. The original paper describing the species, stated it can infect Magnolia and Camellia species, Pieris formosa, Gevuina avellana, Michelia doltsopa and Quercus ilex. Since then many other plants have been identified as natural hosts of the pathogen. Molecular analysis has revealed that an infection on Pinus radiata, recorded in New Zealand in 1950, was caused by P. kernoviae. The pathogen was also noted on Drimys winteri, Gevuina avellana, Ilex aquifolium, Quercus ilex, Vaccinium myrtillus, Hedera helix, Podocarpus salignas.
A wilt disease is any number of diseases that affect the vascular system of plants. Attacks by fungi, bacteria, and nematodes can cause rapid killing of plants, large tree branches or even entire trees.
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.
Fusarium circinatum is a fungal plant pathogen that causes the serious disease pitch canker on pine trees and Douglas firs. The most common hosts of the pathogen include slash pine, loblolly pine, Monterey pine, Mexican weeping pine, and Douglas fir. Like other Fusarium species in the phylum Ascomycota, it is the asexual reproductive state of the fungus and has a teleomorph, Gibberella circinata.
Calophoma clematidina is a fungal plant pathogen and the most common cause of the disease clematis wilt affecting large-flowered varieties of Clematis. Symptoms of infection include leaf spotting, wilting of leaves, stems or the whole plant and internal blackening of the stem, often at soil level. Infected plants growing in containers may also develop root rot.
Hypoxylon canker of shade trees is a weak ascomycete fungus that negatively affects growth and can eventually lead to the death of already dying or diseased host trees. There are many different species that affect different trees. For example, Hypoxylon atropunctatum, a common species, is found on oak trees, Hypoxylon tinctor affects sycamore trees, and Hypoxylon mammatum infests aspen trees.