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Bondarzewia berkeleyi
Bondarzewia berkeleyi
Bondarzewia berkeleyi
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Bondarzewia berkeleyi
Scientific classification Edit this classification
Kingdom: Fungi
Division: Basidiomycota
Class: Agaricomycetes
Order: Russulales
Family: Bondarzewiaceae
Genus: Bondarzewia
Species:
B. berkeleyi
Binomial name
Bondarzewia berkeleyi
(Fr.) Bondartsev & Singer (1941)
Synonyms
  • Polyporus berkeleyi Fr. (1851)

Bondarzewia berkeleyi, commonly known as Berkeley's polypore,[1] or stump blossoms,[2] is a species of polypore fungus in the family Russulaceae. It is a parasitic species that causes butt rot in oaks and other hardwood trees. A widespread fungus, it is found in the Old World and North America.

Taxonomy

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Elias Magnus Fries described the species as Polyporus berkeleyi in 1851. It was moved to the genus Bondarzewia in 1941.[3]

Description

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The fan- or shelf-shaped caps grow in overlapping clumps from the bases of trees, each growing to 20–50 centimetres (8–19+1⁄2 in) diameter.[4] They are zoned in various shades of white to pale grey, cream, beige or yellow.[4] The pore surface is white, as is the spore print. The round spores are 7–9 by 6–8 μm and have marked amyloid ridges. The tough white flesh can be up to 3 cm (1+1⁄4 in) thick and has a mild taste, becoming bitter with age.[4] The outer edges that cut easily with a knife are quite tender.

Similar species

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Potential lookalikes include B. occidentalis, Grifola frondosa, Meripilus sumstinei, and Vanderbylia spp.[4]

Distribution and habitat

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The distribution of B. berkeleyi is widespread, occurring in Europe, Asia, Africa, and North America east of the Great Plains (June–October).[5][6][4] While its primary host is oak, it has also been observed on other hardwood species such as maple.[7]

In China it has been recorded from Guangdong and Hunan provinces.[5][8] The fruit bodies appear over July to October in the United States.[1] A survey of host trees in North Carolina found that it almost always grew on oaks, being recorded from the white oak (Quercus alba), scarlet oak (Q. coccinea), southern red oak (Q. falcata), chestnut oak (Q. prinus) and eastern black oak (Q. velutina), as well as bird cherry (Prunus pensylvanica).[9]

Ecology

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Bondarzewia berkeleyi is a parasitic fungus causing butt rot in oaks and other hardwood trees.[10] It causes a white stringy rot in the roots and heartwood of the lower trunk, typically not extending more than 0.9–1.5 m (3–5 ft) upwards. The decay is mainly restricted to the heartwood, and external symptoms might include excessive tapering or flaring at the base of the trunk, cracks, seams, and sap flow. The fungus is known for its rapid growth rate compared to other wood-rotting fungi common on oaks.[11]

While primarily a parasite, B. berkeleyi can also act as a saprophyte, thriving on dead hardwood trees or stumps. The fruiting bodies typically appear on infected trees in summer and fall.[10]

Edibility

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B. berkeleyi is typically considered edible when young, tender and well cooked, the palatability decreases with age as the flesh becomes tough and bitter.[6] Some sources compare the texture to shoe leather when older,[10] while others suggest that the softer outer edges of older specimens can be consumed.[12] Some field guides list the species as inedible or warn that it may cause gastrointestinal upset or allergic reactions in some individuals.[13][14]

It may be able to be used to strengthen other flavors in dishes, much like tofu. It can also reportedly be used as a meat substitute.[15] Preparation methods often involve parboiling or blanching to remove bitterness, followed by slicing and incorporating into stir-fries or other dishes.

See also

[edit]

References

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[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Bondarzewia berkeleyi

View on Grokipedia
from Grokipedia
Bondarzewia berkeleyi, commonly known as Berkeley's , is a conspicuous species of in the Bondarzewiaceae, order Russulales, characterized by its large, annual, pileate basidiocarps that form imbricate rosettes or clusters up to 1 meter across at the base of hardwood trees. Native exclusively to eastern , it functions primarily as a white-rot on dead angiosperm wood but also acts as a parasite causing butt rot in living hardwoods such as oaks (Quercus spp.) and maples (Acer spp.), weakening tree trunks over time. The produces ochraceous caps with whitish to straw-colored pore surfaces featuring large angular pores (approximately 1 per mm), and its basidiospores measure 6.4–7.5 × 5.2–7 µm with strongly , blunt ornamentation. When young, the firm, white flesh is with a mild, pleasant flavor reminiscent of , though it becomes tough and bitter with age, limiting culinary use to immature specimens. First described as Polyporus berkeleyi by Elias Fries in 1851 and later transferred to the genus Bondarzewia by Bondartsev and Singer in 1941, the species represents the sole member of its in , distinguished phylogenetically from Old World relatives like B. mesenterica through molecular analyses of ITS and LSU rDNA sequences. Ecologically significant in ecosystems, B. berkeleyi contributes to wood and nutrient cycling in deciduous woodlands, fruiting from late summer through fall, often in terrestrial groups on buried roots or stumps. Its imposing size and rosette form make it a notable sight for mycologists and foragers, though proper identification is essential to avoid confusion with similar polypores like , which has smaller pores. While not commercially cultivated, its edibility and role in potential warrant further research into its chemical profile, including secondary metabolites with possible medicinal properties observed in related Bondarzewia species.

Taxonomy

Classification

Bondarzewia berkeleyi is a species of classified within the kingdom Fungi, phylum , class , order Russulales, family Bondarzewiaceae, and genus Bondarzewia. The genus Bondarzewia is distinguished by its annual, pileate basidiocarps featuring poroid hymenophores, which give the fruiting bodies a polypore-like appearance, along with strongly and ornamented basidiospores that exhibit a white rot decay pattern. Phylogenetic analyses based on of the (ITS) regions and the large subunit (LSU) of (28S rDNA D1-D2 domains) have substantiated the current placement of Bondarzewia in the Bondarzewiaceae family under Russulales, supporting its reclassification from the earlier assignment to through molecular evidence of its monophyletic , and confirming B. berkeleyi as the only North American species in the genus, distinct from Eurasian relatives like B. mesenterica. Notable synonyms for B. berkeleyi include Polyporus berkeleyi Fr., reflecting historical taxonomic shifts.

Nomenclature history

The species was first described as Polyporus berkeleyi by Swedish mycologist Magnus Fries in 1851, in his publication Nova Acta Regiae Societatis Scientiarum Upsaliensis, based on specimens collected in and named in honor of the prominent British mycologist Miles Joseph Berkeley (1803–1889). This reflected its initial placement within the broad genus Polyporus, which at the time encompassed many fungi with poroid hymenophores. In 1941, the fungus was reclassified into the newly proposed genus Bondarzewia by Russian mycologist Appolinaris Bondartsev and German mycologist Rolf Singer, recognizing distinct morphological and developmental traits such as its rosette-forming basidiocarps and spores, which distinguished it from other species. This transfer, published in Annales Mycologici, marked a significant genus-level revision amid broader efforts to refine in the early 20th century. Subsequent synonyms included Grifola berkeleyi (Murrill, 1904), reflecting temporary alignments with hen-of-the-woods-like genera. Key taxonomic advancements in the mid-20th century further contextualized Bondarzewia berkeleyi within the family Bondarzewiaceae, initially established by František Kotlaba and Zdeněk Pouzar in 1957 to group fungi with spores in the Russulales order, including the pileate Bondarzewia and resupinate genera. Dutch mycologist Marinus Anton Donk contributed to its consolidation in 1960 through detailed nomenclatural and generic revisions in Persoonia, emphasizing phylogenetic affinities based on spore ornamentation and hyphal structure, which solidified the family's boundaries. Common names for the fungus, such as Berkeley's polypore and stump blossoms, derive directly from its scientific epithet honoring M.J. Berkeley and its habit of forming large, shelf-like clusters at tree bases, evoking floral displays on stumps. These vernacular terms have persisted in North American and European mycological literature since the late .

Description and identification

Macroscopic features

Bondarzewia berkeleyi produces large, annual fruiting bodies that form rosette-like or shelf-shaped clusters at the bases of trees, often consisting of several overlapping, fan-shaped caps arising from a short, central stem-like structure. Individual caps measure 6–25 cm across, though entire clusters can span 20–50 cm or more, occasionally reaching up to 1 m in diameter in exceptional cases. These structures are typically found attached to trees such as oaks, emerging from the soil or directly from the trunk base. The cap surface is dry and leathery to velvety in texture, often featuring irregular zones, radial wrinkles, or cracks, with wavy, rolled margins. Coloration starts white to cream when young, fading to pale buff, tan, or dull yellowish with age, sometimes developing brownish stains. The underside bears a white pore surface with large, angular pores numbering 1–2 per mm (0.5–1 mm diameter), which become slightly larger and more irregular over time; the tubes are shallow, less than 1 cm deep. The flesh is thick, white, and tough to corky, remaining firm and succulent when fresh but hardening upon drying. Young specimens emit a mild, not distinctive odor, while the taste is mild initially but can become bitter or acrid in mature fruiting bodies. Fruiting occurs annually from late summer through fall, typically July to October in North America.

Microscopic features

The basidiospores of Bondarzewia berkeleyi are subglobose to globose, measuring 6–7.5 × 5–7 μm, hyaline, and ornamented with short, blunt ridges that are strongly amyloid, turning blue in Melzer's reagent. These spores produce a white spore print, aiding in preliminary identification. Basidia are club-shaped (clavate), 40–50 × 7.5–12 μm, thin-walled, and typically bear four sterigmata. The hyphal system is dimitic, comprising hyaline thin-walled generative hyphae lacking clamps and thick-walled aseptate skeletal hyphae. Cystidia are absent from the hymenium and context.

Similar species

Bondarzewia berkeleyi can be distinguished from the western North American Bondarzewia occidentalis (formerly known as Bondarzewia mesenterica), which is typically smaller with yellowish to tan caps and occurs primarily on conifers rather than hardwoods. Unlike Ganoderma applanatum, which features a woody, shelf-like fruiting body with a furrowed, brownish upper surface lacking the rosetted form and white coloration of B. berkeleyi, and possesses non-amyloid, brown spores in contrast to the amyloid, white spores of B. berkeleyi. Differentiation from Meripilus sumstinei relies on the latter's smaller, tiered rosettes with black-edged, zonate caps that bruise intensely black upon handling, whereas B. berkeleyi forms larger, flatter rosettes of unbruising, cream-white caps without such zoning. Among eastern North American polypores, the massive size (often exceeding 50 cm across), persistent white coloration, and basal attachment to hardwood trunks are unique to B. berkeleyi. In the field, the absence of black resinous zones or crusts helps separate it from species like Heterobasidion annosum, which may exhibit such features on conifer bases. The amyloid reaction of B. berkeleyi spores further confirms identification under microscopy.

Distribution and habitat

Geographic range

Bondarzewia berkeleyi is native to eastern east of the , extending from southern through the to the southeastern states such as . In this region, the fungus is commonly documented in forested areas and woodlands, where it contributes to wood decomposition processes. The species exhibits potential for range expansion within , with establishing populations noted in urban forests and southern states, likely facilitated by human-mediated dispersal through trade in ornamental hardwoods and landscape plantings. This has led to sightings in anthropogenic environments within its native range. Fruiting occurs seasonally in the , typically from summer through autumn ( to ), aligning with favorable moisture and temperature conditions in temperate climates. Recent data, particularly from platforms like since 2020, have documented new occurrences in southern U.S. states such as and Georgia, suggesting ongoing southward expansion possibly influenced by climate shifts or human-mediated dispersal.

Substrate and environmental preferences

Bondarzewia berkeleyi primarily colonizes living hardwoods, with a strong preference for oaks (Quercus spp.), though it also occurs on maples ( spp.), beeches (Fagus spp.), hickories (Carya spp.), and other deciduous trees such as honeylocusts (*). It typically fruits at the bases of mature trees, on exposed roots, or from buried wood and stumps, functioning as both a parasite on living hosts and a saprobe on decaying material. This fungus thrives in moist, shaded environments, often appearing in clusters following periods of high humidity and rainfall during late summer and fall. It is commonly found in temperate forests across eastern , tolerating a range of settings from stands to more open areas near tree bases. B. berkeleyi demonstrates adaptability to urban and managed landscapes, occurring on stressed trees in parks, plantations, and residential areas, particularly where oaks and other hardwoods are present. Fruiting bodies emerge from July to October in regions like the Midwest and Northeast, persisting or reappearing in the same locations for multiple years under suitable conditions.

Ecology

Pathogenic interactions

_Bondarzewia berkeleyi acts as a primary pathogen, causing white rot known as butt rot in the roots and lower heartwood of living trees. This decay involves the degradation of lignin and cellulose, resulting in a characteristic white, stringy texture that weakens the structural integrity of the affected wood. The fungus typically infects through root contacts or wounds at the base of the tree, with decay generally confined to the lower 3–5 feet of the trunk and extensive root systems. Infected trees exhibit symptoms such as basal swelling (bottle butt), cracks, seams, and sap flow, leading to reduced vigor and increased susceptibility to mechanical failure, including . As a white-rot fungus, B. berkeleyi employs oxidative enzymes like laccases and peroxidases to facilitate wood degradation, a mechanism conserved across white-rot and demonstrated in its efficient delignification of lignocellulosic substrates. Trees do not recover from established infections, often progressing to death over extended periods. The fungus shows host specificity primarily for oaks (Quercus spp.) and other hardwoods, though it can affect species like maples. In forestry contexts, it poses significant economic impacts by compromising timber quality through heartwood degradation and necessitating monitoring in oak-dominated ecosystems, particularly in eastern where it is a common and destructive agent in both natural forests and managed landscapes. No effective chemical controls exist, emphasizing the importance of preventive measures like maintaining tree health to mitigate spread.

Reproduction and life cycle

_Bondarzewia berkeleyi exhibits a typical basidiomycete life cycle characteristic of wood-decay polypores, involving both sexual and limited phases. The persists as a within the roots and lower trunk of trees, where it colonizes and decomposes wood over extended periods, often lasting more than 10 years. Establishment of the following typically requires several years before fruiting bodies form. Sexual reproduction is initiated annually when the established mycelium produces fruiting bodies—large, rosette-like structures—emerging from soil or wood near the base of host trees in late summer to early fall. These fruiting bodies mature over 1–2 weeks, developing from initial primordia to full spore-producing maturity. Basidiospores form on basidia lining the white pores on the underside of the caps; the spores are globose to subglobose, measuring 6–7.5 µm, with densely packed amyloid spines 1–2 µm long, and produce a white spore print. These basidiospores are primarily wind-dispersed over short distances, facilitating local propagation. Upon dispersal, basidiospores germinate on suitable woody substrates, with lab studies indicating within 24–48 hours on media under controlled conditions. The resulting haploid primary grows vegetatively, eventually fusing with compatible hyphae to form dikaryotic secondary that sustains colonization. is minimal but occurs through fragmentation of the , which aids in local spread via contacts or movement. This life cycle supports the fungus's role in nutrient cycling while linking to pathogenic interactions like butt rot in infected trees.

Edibility and uses

Culinary preparation

Bondarzewia berkeleyi is considered edible only when young, typically within the first 1-2 weeks of fruiting when the caps are small, supple, and the outer edges are tender and easy to cut. At this stage, the interior flesh is white, thick, and soft, offering a mild, nutty flavor reminiscent of chicken of the woods (Laetiporus sulphureus), though less tart. Older specimens develop a tough, woody texture and a bitter taste, rendering them unpalatable. Harvesting should focus on young rosettes found at the bases of trees such as oaks or maples, ideally in late summer to early fall. Collectors should cut the entire rosette carefully to avoid damaging the substrate, then separate the individual caps and discard the tough central stem and inner portions, retaining only the tender 1-2 inch margins. Modern guides from the 2020s stress selecting these immature specimens to achieve the best texture and flavor, as maturity quickly diminishes quality. Preparation involves slicing the tender parts thinly, no more than 1/8 to 1/4 inch thick, to ensure even cooking and tenderness. Common methods include in butter or oil with herbs like to enhance the mild earthy notes, into cutlets, or incorporating into soups where the pieces are browned first for depth. The can also be dried and ground into powders for seasoning, though spices are often added to counter any subtle bitterness. Always cook thoroughly, as raw consumption may cause digestive discomfort. Recipes such as duxelles or with lemon highlight its meaty texture when young, serving as a versatile substitute. Nutritionally, on a dry weight basis, Bondarzewia berkeleyi shares the profile typical of s, with high protein content ranging from 20-30%, substantial , and low caloric value, making it a nutrient-dense option for low-energy diets.

Potential risks and precautions

While Bondarzewia berkeleyi is generally considered non-toxic, consuming large quantities, particularly of older or bitter specimens, may lead to minor gastrointestinal upset in sensitive individuals. Young fruiting bodies are preferred for edibility to minimize bitterness and potential digestive discomfort. As with any wild , individual sensitivities may occur, so caution is advised during . Accurate identification is essential to avoid confusion with toxic look-alikes, and beginners should consult mycological experts or field guides before consumption. Starting with small amounts is recommended to test for personal sensitivities, as individual reactions can vary. Thorough cooking is advised to enhance digestibility, though no specific compounds like oxalates have been widely documented as requiring breakdown in this species. Environmentally, overharvesting of wild fungi, including B. berkeleyi, poses risks to fungal populations and forest ecosystems, particularly in accessible urban areas where demand may exceed sustainable yields. Specimens from polluted sites should be avoided, as the fungus can absorb and contaminants from , potentially concentrating them in edible tissues. Further research is needed to explore any potential therapeutic applications, and is not recommended.

References

  1. https://mushroomexpert.com/bondarzewia_berkeleyi.html
  2. https://pmc.ncbi.nlm.nih.gov/articles/PMC5041112/
  3. https://chrisluleyphd.com/wp-content/uploads/2022/02/9.-Luley_Dirty-Rotten-Decay-Fungi_from-TCI-Mag-Series.pdf
  4. https://ultimate-mushroom.com/edible/1211-bondarzewia-berkeleyi.html
  5. https://www.mushroom-appreciation.com/introduction-to-polypores.html
  6. https://www.mycobank.org/page/Name%20details%20page/name/Bondarzewia%20berkeleyi
  7. https://mdc.mo.gov/discover-nature/field-guide/berkeleys-polypore
  8. https://alabamamushroomsociety.org/Bondarzewia-berkeleyi
  9. https://pmc.ncbi.nlm.nih.gov/articles/PMC11044139/
  10. https://www.gbif.org/species/2552027
  11. https://www.indexfungorum.org/names/namesrecord.asp?RecordID=185446
  12. https://www.mykoweb.com/systematics/literature/NAF_Vol9Part1_7.pdf
  13. https://www.indexfungorum.org/names/namesrecord.asp?RecordID=293765
  14. https://msu-prod.dotcmscloud.com/news/bondarzewia-berkeleyi
  15. https://www.mycobank.org/details/708/58831
  16. https://www.jstor.org/stable/4179442
  17. https://www.mushroomexpert.com/bondarzewia_berkeleyi.html
  18. https://www.fs.usda.gov/pnw/pubs/pnw_gtr476.pdf
  19. https://www.researchgate.net/publication/301534437_Molecular_phylogeny_and_global_diversity_of_the_remarkable_genus_Bondarzewia_Basidiomycota_Russulales
  20. https://www.tandfonline.com/doi/full/10.3852/09-050
  21. https://www.mushroomexpert.com/ganoderma_applanatum.html
  22. https://mdc.mo.gov/discover-nature/field-guide/black-staining-polypore
  23. https://www.inaturalist.org/taxa/20731-Bondarzewia-berkeleyi
  24. https://www.umass.edu/agriculture-food-environment/landscape/fact-sheets/root-butt-rot-caused-by-bondarzewia-berkeleyi-berkeleys-polypore
  25. https://zombiemyco.com/pages/berkeleys-polypore-bondarzewia-berkeleyi
  26. https://bygl.osu.edu/node/588
  27. https://www.mushroom-appreciation.com/berkeleys-polypore.html
  28. https://pmc.ncbi.nlm.nih.gov/articles/PMC7406137/
  29. https://pmc.ncbi.nlm.nih.gov/articles/PMC239084/pdf/aem00133-0013.pdf
  30. https://forestpathology.org/general/fungi/
  31. https://tcimag.tcia.org/training/here-come-the-basidiocarps-seasonal-fruiting-of-decay-fungi/
  32. https://nhgardensolutions.wordpress.com/tag/berkleys-polypore/
  33. https://foragerchef.com/berkeleys-polypore-bondarzewia-berkeleyi/
  34. https://pmc.ncbi.nlm.nih.gov/articles/PMC9654758/
  35. https://picturemushroom.com/wiki/Bondarzewia_berkeleyi.html
  36. https://www.researchgate.net/publication/363212112_Species_Richness_Morphological_Features_and_Inventory_of_Wild_Macrofungi_found_in_Akwa_Ibom_State_Nigeria
  37. https://www.fao.org/3/y5489e/y5489e.pdf
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