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Exsudoporus frostii

Exsudoporus frostii
Scientific classification
Domain: Eukaryota
Kingdom: Fungi
Division: Basidiomycota
Class: Agaricomycetes
Order: Boletales
Family: Boletaceae
Genus: Exsudoporus
Species:
E. frostii
Binomial name
Exsudoporus frostii
(J.L.Russell) Vizzini, Simonini & Gelardi (2014)
Synonyms[1]
  • Boletus frostii J.L.Russell (1874)
  • Suillellus frostii (J.L.Russell) Murrill (1909)
  • Tubiporus frostii (J.L.Russell) S.Imai (1968)
  • Butyriboletus frostii (J.L. Russell) G. Wu, Kuan Zhao & Zhu L. Yang (2016)
Exsudoporus frostii
Pores on hymenium
Cap is convex or flat
Hymenium is adnate
Stipe is bare
Spore print is olive-brown
Ecology is mycorrhizal
Edibility is edible

Exsudoporus frostii (formerly Boletus frostii), commonly known as Frost's bolete or the apple bolete, is a bolete fungus first described scientifically in 1874. A member of the family Boletaceae, the mushrooms produced by the fungus have tubes and pores instead of gills on the underside of their caps. Exsudoporus frostii is distributed in the eastern United States from Maine to Georgia, and in the southwest from Arizona extending south to Mexico and Costa Rica. A mycorrhizal species, its fruit bodies are typically found growing near hardwood trees, especially oak.

Exsudoporus frostii mushrooms can be recognized by their dark red sticky caps, the red pores, the network-like pattern of the stipe, and the bluing reaction to tissue injury. Another characteristic of young, moist fruit bodies is the amber-colored drops exuded on the pore surface. Although the mushrooms are considered edible, they are generally not recommended for consumption because of the risk of confusion with other poisonous red-pored, blue-bruising boletes. B. frostii may be distinguished from other superficially similar red-capped boletes by differences in distribution, associated tree species, bluing reaction, or morphology.

Taxonomy edit

The species was named by the Unitarian minister John Lewis Russell of Salem, Massachusetts, based on specimens found in Brattleboro, Vermont. He named the fungus after his friend, fellow amateur American mycologist Charles Christopher Frost, who published a description of the species in his 1874 survey of the boletes of New England.[2][3] When the name of a species is contributed by an individual, but the name is formally published by another, the contributor's name can be cited, separated from the publishing author as apud; for this reason, the name and authority are written Boletus Frostii Russell apud Frost in some older literature.[4] Bernard Ogilvie Dodge made reference to B. frostii in 1950 during an address to the Mycological Society of America, in which he spoke about the role of the amateur in discovering new species: "They would have informed us all about the man Russell, who named a fine new bolete for his friend Frost, and about the man Frost, who named a fine new bolete for his friend Russell. Boletus Frostii and Boletus Russellii are mushrooms with character, even though they were described by amateurs."[5] However, in attempting to establish a lectotype specimen, mycologist Roy Halling examined both Russell's original material and his accompanying notes; he concluded that it was Frost who made the original species determinations, further suggesting that "there is no evidence to show that Russell ever collected B. frostii or wrote a description of it."[6]

William Murrill in 1909 placed the species in the genus Suillellus,[7] while Sanshi Imai transferred it to Tubiporus in 1968.[1] Tubiporus has since been synonymized with Boletus.[8] In 1945, Rolf Singer described a bolete he found in Florida; although he originally described it as a subspecies of B. frostii,[9] he later considered the differences between the taxa significant enough to warrant publishing Boletus floridanus as a unique species.[4] Following the molecular studies that outlined a new phylogenetic framework for the Boletaceae,[10][11] the bolete was transferred to the newly circumscribed genus Exsudoporus in 2014.[12]

Due to lack of sufficient sequences, Wu and colleagues (2016) were reluctant to accept Exsudoporus and considered it a synonym of Butyriboletus, so they transferred E. frostii to the genus Butyriboletus and proposed a new combination Butyriboletus frostii.[13] However, following phylogenetic and morphological analyses clearly resolved Exsudoporus as a monophyletic, homogenous and independent genus that is sister to Butyriboletus.[14][15]

Exsudoporus frostii is commonly known as "Frost's bolete"[16] or the "apple bolete". In Mexico, its vernacular name is panza agria, which translates to "sour belly".[17]

Description edit

The shape of the cap of the young fruit body ranges from a half sphere to convex, later becoming broadly convex to flat or shallowly depressed, with a diameter of 5–15 cm (2.0–5.9 in).[18] The edge of the cap is curved inward, although as it ages it can uncurl and turn upward. In moist conditions, the cap surface is sticky as a result of its cuticle, which is made of gelatinized hyphae. If the fruit body has dried out after a rain, the cap is especially shiny,[4] sometimes appearing finely areolate (having a pattern of block-like areas similar to cracked, dried mud).[18] Young mushrooms have a whitish bloom on the cap surface.[19]

 
View of the hymenium

The color is bright red initially, but fades with age. The flesh is up to 2.5 cm (1.0 in) thick, and ranges in color from pallid to pale yellow to lemon yellow.[18] The flesh has a variable staining reaction in response to bruising, so some specimens may turn deep blue almost immediately, while others turn blue weakly and slowly.[4]

The tubes comprising the pore surface (the hymenium) are 9–15 mm deep, yellow to olivaceous yellow (mustard yellow), turning dingy blue when bruised. The pores are small (2 to 3 per mm), circular, and until old age a deep red color that eventually becomes paler. The pore surface is often beaded with yellowish droplets when young (a distinguishing characteristic), and readily stains blue when bruised. The stipe is 4 to 12 cm (1.6 to 4.7 in) long, and 1 to 2.5 cm (0.4 to 1.0 in) thick at its apex. It is roughly equal in thickness throughout its length, though it may taper somewhat toward the top; some specimens may appear ventricose (swollen in the middle).[18] The stipe surface is mostly red, or yellowish near the base; it is reticulate—characterized by ridges arranged in the form of a net-like pattern.[18] Mycelia, visible at the base of the stipe, are yellowish white to light yellow.[4]

 
Young fruit bodies may secrete an amber liquid.

The spore print of B. frostii is olive brown.[18] The spores are thick walled, smooth, and spindle shaped, with dimensions of 11–15 by 4–5 µm. Longer spores up to 18 µm long may also be present.[18] The cap cuticle, or pileipellis, is made of a tangled layer of gelatinized hyphae that are 3–6 µm wide.[20] The spore-bearing cells, the basidia, are four spored and measure 26–35 by 10.5–11.5 µm. Cystidia are non-fertile cells interspersed among the basidia, and they are prevalent in the hymenial tissue of E. frostii. These hyaline (translucent) cells measure 30–53 long by 7.5–14 µm wide, and range in shape from somewhat like a spindle (tapering at each end, but with one end typically rounded) to subampullaceous—shaped somewhat like a swollen bottle.[4]

Edibility and nutritional composition edit

This species is nonpoisonous.[21] Murrill wrote in 1910 of its edibility: "Usually viewed with suspicion because of its red hymenium, but its properties are not accurately known."[22] Since then, several authors have advised against consuming the species, due to its resemblance to other toxic red-capped boletes.[16][18][23] In his 100 Edible Mushrooms (2007), Michael Kuo notes that although the mushroom is apparently edible for some, it "affects others negatively".[24] David Arora mentions that it is commonly sold in rural markets in Mexico;[17] a 1997 study suggests that it is only consumed in rural areas in Querétaro state.[25] Its taste and odor have been described as "pleasant"[16] or "sweet"[21] and somewhat like citrus,[19] although the cuticle of the cap may taste acidic.[18]

Chemical analysis of fresh fruit bodies collected in Mexico showed them to have the following composition: moisture 94.53%; ash 0.323%; dietary fiber 3.024%; fat 0.368%; and protein 1.581%. The free fatty acid content of dried fruit bodies was 4.5%, slightly more than the common button mushroom (Agaricus bisporus), which had 3.5%. The majority of this total was oleic acid (1.95%), followed by linoleic acid (1.68%) and palmitic acid (1.69%).[25]

Similar species edit

 
Poisonous Boletus flammans is similar in appearance.

Other red-capped boletes include the poisonous B. flammans and B. rubroflammeus; the former grows most commonly under conifers, the latter in association with hardwoods in eastern North America and southern Arizona.[17] Often confused with Exsudoporus floridanus and E. permagnificus, but the latter species is known only from Europe and Western Asia and always grow in association with oaks and occasionally also with sweet chestnut.[26][27][15] Exsudoporus floridanus differs from E.  frostii in having a lighter cap color and in the texture of the cap surface: it is tomentose (covered with dense, short, soft, matted hairs) or velutinous (like velvet), compared to the relatively smooth surface of E. frostii. Singer notes that although the physical characteristics between the two taxa may be blurred and are hard to define, the area of origin can reliably distinguish them: E. floridanus is found on shaded lawns and scrubland in open oak stands in non-tropical regions of Florida, typically on grassy or sandy soil, where it fruits between May and October.[4]

The fruit bodies of young specimens of B. kermesinus, newly described from Japan in 2011, are similar in appearance to E. frostii. In addition to its distribution, B. kermesinus can be distinguished from E. frostii by having flesh that does not bruise blue and a stipe in which the reticulum is not as deep and coarse.[28] B. pseudofrostii, found in Belize, produces smaller caps that are 1.7 to 2.0 cm (0.7 to 0.8 in) in diameter.[29] Boletus russelli, found in eastern North America, has a red to reddish-brown cap and reticulate stipe, but its pore surface is yellow, and the fruit body does not bruise blue.[24]

Ecology, habitat, and distribution edit

 
Immature specimen with cap not fully expanded; bruising is evident on the stipe.

Exsudoporus frostii is a mycorrhizal species,[30] meaning that the fungus forms associations with the roots of various species of trees. These associations are mutualistic, because the fungus absorbs mineral nutrients from the soil and channels these into the plant, while the plant provides the fungus with sugars, a product of photosynthesis. The characteristic feature of the mycorrhiza is the presence of a sheath of fungal tissue that encases the terminal, nutrient-absorbing rootlets of the host plant. The fungus forms an extensive underground network of hyphae that radiate outward from the surface of the root sheath, effectively increasing the surface area for nutrient absorption. The hyphae also invade between the root cortical cells to form a Hartig net.[31] Using pure culture techniques, Exsudoporus frostii has been shown to form mycorrhizae with Virginia pine (Pinus virginiana),[30] while a field study confirms a similar association with the oak Quercus laurina.[32]

The fruit bodies grow solitarily, scattered, or in groups on the ground under hardwood trees; the fungus fruits in summer to early autumn. William Murrill noted its preference for growing in "thin oak woods, where the light is sufficient to enable grass to grow",[7] and Alexander H. Smith mentioned its preference for growing in "thin, sandy soil under scrub oak."[3] In the United States, it is distributed from Maine south to Georgia, extending west to Tennessee and Michigan, and in southern Arizona.[4][19] In Mexico, it is often found under Madrone.[17] It has also been collected in Costa Rica, where it associates with the oak species Quercus copeyensis, Q. costaricensis, Q. rapurahuensis, and Q. seemanii.[33] A 1980 publication tentatively suggested that the fungus was also present in Italy,[34] but the author later determined that the putative E. frostii was actually Boletus siculus.[27]

Fruit bodies can be parasitized by the mold-like fungus Sepedonium ampullosporum.[35] Infection results in necrosis of the mushroom tissue, and a yellow color caused by the formation of large amounts of pigmented aleurioconidia (single-celled conidia produced by extrusion from the conidiophores).[36]

See also edit

References edit

  1. ^ a b "Boletus frostii J.L. Russell". MycoBank. International Mycological Association. Retrieved 2011-06-21.
  2. ^ Frost CC. (1874). "Catalogue of Boleti of New England, with descriptions of new species". Bulletin of the Buffalo Society of Natural Sciences. 2: 100–5.
  3. ^ a b Weber NS, Smith AH (1980). The Mushroom Hunter's Field Guide. Ann Arbor, Michigan: University of Michigan Press. pp. 104–5. ISBN 0-472-85610-3.
  4. ^ a b c d e f g h Singer R. (1947). "The Boletoideae of Florida with notes on extralimital species III". American Midland Naturalist. 37 (1): 77–8. doi:10.2307/2421647. JSTOR 2421647.
  5. ^ Dodge BO. (1952). "The fungi come into their own". Mycologia. 44 (3): 273–91. doi:10.1080/00275514.1952.12024197. JSTOR 4547605.
  6. ^ Halling RE. (1983). "Boletes described by Charles C. Frost". Mycologia. 75 (1): 70–92. doi:10.2307/3792925. JSTOR 3792925.
  7. ^ a b Murrill WA. (1909). "The Boletaceae of North America". Mycologia. 1 (1): 4–18. doi:10.2307/3753167. JSTOR 3753167.
  8. ^ Kirk PM, Cannon PF, Minter DW, Stalpers JA (2008). Dictionary of the Fungi (10th ed.). Wallingford, UK: CAB International. pp. 672, 709. ISBN 978-0-85199-826-8.
  9. ^ Singer R. (1945). "New Boletaceae from Florida (a preliminary communication)". Mycologia. 37 (6): 797–9. doi:10.2307/3755143. JSTOR 3755143.
  10. ^ Nuhn ME, Binder M, Taylor AFS, Halling RE, Hibbett DS (2013). "Phylogenetic overview of the Boletineae". Fungal Biology. 117 (7–8): 479–511. doi:10.1016/j.funbio.2013.04.008. PMID 23931115.
  11. ^ Wu G, Feng B, Xu J, Zhu X-T, Li Y-C, Zeng N-K, Hosen MI, Yang ZL (2014). "Molecular phylogenetic analyses redefine seven major clades and reveal 22 new generic clades in the fungal family Boletaceae". Fungal Diversity. 69 (1): 93–115. doi:10.1007/s13225-014-0283-8. S2CID 15652037.
  12. ^ Vizzini A. (August 22, 2014). "Nomenclatural novelties" (PDF). Index Fungorum (183): 1.
  13. ^ Wu, Gang; Li, Yan-Chun; Zhu, Xue-Tai; Zhao, Kuan; Han, Li-Hong; Cui, Yang-Yang; Li, Fang; Xu, Jian-Ping; Yang, Zhu L. (November 2016). "One hundred noteworthy boletes from China". Fungal Diversity. 81 (1): 25–188. doi:10.1007/s13225-016-0375-8. ISSN 1560-2745. S2CID 22506275.
  14. ^ Loizides M, Bellanger JM, Assyov B, Moreau PA, Richard F (2019). "Present status and future of boletoid fungi (Boletaceae) on the island of Cyprus: cryptic and threatened diversity unraveled by 10-year study". Fungal Ecology. 41 (13): 65–81. doi:10.1016/j.funeco.2019.03.008. S2CID 181958289.
  15. ^ a b Biketova AY, Gelardi M, Smith ME, Simonini G, Healy RA, Taneyama Y, Vasquez G, Kovács Á, Nagy LG, Wasser SP, Peintner U, Nevo E, Bunyard BA, Vizzini A (2022). "Reappraisal of the Genus Exsudoporus (Boletaceae) Worldwide Based on Multi-Gene Phylogeny, Morphology and Biogeography, and Insights on Amoenoboletus". Journal of Fungi. 8 (2): 2–25. doi:10.3390/jof8020101. PMC 8874676. PMID 35205856.
  16. ^ a b c Phillips R. . Rogers Plants. Archived from the original on 2012-02-18. Retrieved 2012-03-01.
  17. ^ a b c d Arora D. (1986). Mushrooms Demystified: A Comprehensive Guide to the Fleshy Fungi. Berkeley, California: Ten Speed Press. p. 529. ISBN 0-89815-169-4.
  18. ^ a b c d e f g h i Thiers HD, Smith AH (1971). The Boletes of Michigan. Ann Arbor, Michigan: University of Michigan Press. pp. 343–4. ISBN 0-472-85590-5.
  19. ^ a b c Bessette AE, Roody WC, Bessette AR (2000). Boletes of North America. Syracuse, New York: Syracuse University Press. p. 114. ISBN 978-0-8156-0588-1.
  20. ^ Kuo M. (January 2007). "Boletus frostii". MushroomExpert.Com. Retrieved 2012-03-01.
  21. ^ a b Miller HR, Miller OK (2006). North American Mushrooms: A Field Guide to Edible and Inedible Fungi. Guilford, Connecticut: FalconGuide. p. 385. ISBN 978-0-7627-3109-1.
  22. ^ Murrill WA. (1910). "Poisonous mushrooms". Mycologia. 2 (6): 255–64. doi:10.2307/3753292. JSTOR 3753292.
  23. ^ Bessette A, Miller OK Jr, Bessette AR, Miller HR (1995). Mushrooms of North America in Color: A Field Guide Companion to Seldom-Illustrated Fungi. Syracuse, New York: Syracuse University Press. p. 385. ISBN 0-8156-2666-5.
  24. ^ a b Kuo M. (2007). 100 Edible Mushrooms. Ann Arbor, Michigan: The University of Michigan Press. pp. 121–2. ISBN 978-0-472-03126-9.
  25. ^ a b León-Guzmán MF, Silva I, López MG (1997). "Proximate chemical composition, free amino acid contents, and free fatty acid contents of some wild edible mushrooms from Querétaro, México". Journal of Agricultural and Food Chemistry. 45 (11): 4329–32. doi:10.1021/jf970640u.
  26. ^ Pöder R. (1981). "Boletus permagnificus spec. nov. – ein auffallender Röhrling der Sektion Luridi Fr. assoziiert mit Eichen" [Boletus permagnificus new species – a striking bolete of the section Luridi associated with oak]. Sydowia (in German). 34: 149–56. ISSN 0082-0598.
  27. ^ a b Alessio CL. (1981). "Boletus siculus inzenga il gia presunto B. frostii Russell rinvenuto in Italia" [Boletus siculus is the supposed Boletus frostii discovered in Italy]. Micologia Italiana (in Italian). 10 (2): 40–2.
  28. ^ Takahashi H, Taneyama Y, Koyama A (2011). "Boletus kermesinus, a new species of Boletus section Luridi from central Honshu, Japan". Mycoscience. 52 (6): 419–24. doi:10.1007/s10267-011-0119-2. S2CID 83544311.
  29. ^ Ortiz-Santana B, Lodge DJ, Baroni TJ, Both EE (2007). "Boletes from Belize and the Dominican Republic" (PDF). Fungal Diversity. 27 (2): 247–416 (see p. 322).
  30. ^ a b Vozzo JA, Hackskaylo E (1961). "Mycorrhizal fungi on Pinus virginiana". Mycologia. 53 (5): 538–9. doi:10.2307/3756310. JSTOR 3756310.
  31. ^ Deacon J. (2005). Fungal Biology. Cambridge, Massachusetts: Blackwell Publishers. pp. 262–3. ISBN 1-4051-3066-0.
  32. ^ Morris MH, Pérez-Pérez MA, Smith ME, Bledsoe CS (2009). "Influence of host species on ectomycorrhizal communities associated with two co-occurring oaks (Quercus spp.) in a tropical cloud forest". FEMS Microbiology Ecology. 69 (2): 274–87. doi:10.1111/j.1574-6941.2009.00704.x. PMID 19508503.
  33. ^ Halling RE, Muller GM. "Boletus frostii". Macrofungi of Costa Rica. New York Botanical Garden. Retrieved 2011-09-29.
  34. ^ Alessio CL. (1980). "Boletus Frostii presente in Italia?" [Boletus frostii present in Italy?]. Micologia Italiana (in Italian). 9 (3): 15–20. ISSN 0390-0460.
  35. ^ Sahr T, Ammer H, Besl H, Fischer M (1999). . Mycologia. 91 (6): 935–43. doi:10.2307/3761625. JSTOR 3761625. Archived from the original on 2015-09-23. Retrieved 2011-06-21.
  36. ^ Neuhof T, Berg A, Besl H, Schweche T, Dieckmann R, von Döhren H (2007). "Peptaibol production by Sepedonium strains parasitizing Boletales". Chemistry & Biodiversity. 4 (6): 1103–15. doi:10.1002/cbdv.200790099. PMID 17589879. S2CID 40865857.

External links edit

  • Mushroom Observer Photographs

exsudoporus, frostii, scientific, classificationdomain, eukaryotakingdom, fungidivision, basidiomycotaclass, agaricomycetesorder, boletalesfamily, boletaceaegenus, exsudoporusspecies, frostiibinomial, name, russell, vizzini, simonini, gelardi, 2014, synonyms, . Exsudoporus frostiiScientific classificationDomain EukaryotaKingdom FungiDivision BasidiomycotaClass AgaricomycetesOrder BoletalesFamily BoletaceaeGenus ExsudoporusSpecies E frostiiBinomial nameExsudoporus frostii J L Russell Vizzini Simonini amp Gelardi 2014 Synonyms 1 Boletus frostii J L Russell 1874 Suillellus frostii J L Russell Murrill 1909 Tubiporus frostii J L Russell S Imai 1968 Butyriboletus frostii J L Russell G Wu Kuan Zhao amp Zhu L Yang 2016 Exsudoporus frostiiMycological characteristicsPores on hymeniumCap is convex or flatHymenium is adnateStipe is bareSpore print is olive brownEcology is mycorrhizalEdibility is edible Exsudoporus frostii formerly Boletus frostii commonly known as Frost s bolete or the apple bolete is a bolete fungus first described scientifically in 1874 A member of the family Boletaceae the mushrooms produced by the fungus have tubes and pores instead of gills on the underside of their caps Exsudoporus frostii is distributed in the eastern United States from Maine to Georgia and in the southwest from Arizona extending south to Mexico and Costa Rica A mycorrhizal species its fruit bodies are typically found growing near hardwood trees especially oak Exsudoporus frostii mushrooms can be recognized by their dark red sticky caps the red pores the network like pattern of the stipe and the bluing reaction to tissue injury Another characteristic of young moist fruit bodies is the amber colored drops exuded on the pore surface Although the mushrooms are considered edible they are generally not recommended for consumption because of the risk of confusion with other poisonous red pored blue bruising boletes B frostii may be distinguished from other superficially similar red capped boletes by differences in distribution associated tree species bluing reaction or morphology Contents 1 Taxonomy 2 Description 2 1 Edibility and nutritional composition 2 2 Similar species 3 Ecology habitat and distribution 4 See also 5 References 6 External linksTaxonomy editThe species was named by the Unitarian minister John Lewis Russell of Salem Massachusetts based on specimens found in Brattleboro Vermont He named the fungus after his friend fellow amateur American mycologist Charles Christopher Frost who published a description of the species in his 1874 survey of the boletes of New England 2 3 When the name of a species is contributed by an individual but the name is formally published by another the contributor s name can be cited separated from the publishing author as apud for this reason the name and authority are written Boletus Frostii Russell apud Frost in some older literature 4 Bernard Ogilvie Dodge made reference to B frostii in 1950 during an address to the Mycological Society of America in which he spoke about the role of the amateur in discovering new species They would have informed us all about the man Russell who named a fine new bolete for his friend Frost and about the man Frost who named a fine new bolete for his friend Russell Boletus Frostii and Boletus Russellii are mushrooms with character even though they were described by amateurs 5 However in attempting to establish a lectotype specimen mycologist Roy Halling examined both Russell s original material and his accompanying notes he concluded that it was Frost who made the original species determinations further suggesting that there is no evidence to show that Russell ever collected B frostii or wrote a description of it 6 William Murrill in 1909 placed the species in the genus Suillellus 7 while Sanshi Imai transferred it to Tubiporus in 1968 1 Tubiporus has since been synonymized with Boletus 8 In 1945 Rolf Singer described a bolete he found in Florida although he originally described it as a subspecies of B frostii 9 he later considered the differences between the taxa significant enough to warrant publishing Boletus floridanus as a unique species 4 Following the molecular studies that outlined a new phylogenetic framework for the Boletaceae 10 11 the bolete was transferred to the newly circumscribed genus Exsudoporus in 2014 12 Due to lack of sufficient sequences Wu and colleagues 2016 were reluctant to accept Exsudoporus and considered it a synonym of Butyriboletus so they transferred E frostii to the genus Butyriboletus and proposed a new combination Butyriboletus frostii 13 However following phylogenetic and morphological analyses clearly resolved Exsudoporus as a monophyletic homogenous and independent genus that is sister to Butyriboletus 14 15 Exsudoporus frostii is commonly known as Frost s bolete 16 or the apple bolete In Mexico its vernacular name is panza agria which translates to sour belly 17 Description editThe shape of the cap of the young fruit body ranges from a half sphere to convex later becoming broadly convex to flat or shallowly depressed with a diameter of 5 15 cm 2 0 5 9 in 18 The edge of the cap is curved inward although as it ages it can uncurl and turn upward In moist conditions the cap surface is sticky as a result of its cuticle which is made of gelatinized hyphae If the fruit body has dried out after a rain the cap is especially shiny 4 sometimes appearing finely areolate having a pattern of block like areas similar to cracked dried mud 18 Young mushrooms have a whitish bloom on the cap surface 19 nbsp View of the hymeniumThe color is bright red initially but fades with age The flesh is up to 2 5 cm 1 0 in thick and ranges in color from pallid to pale yellow to lemon yellow 18 The flesh has a variable staining reaction in response to bruising so some specimens may turn deep blue almost immediately while others turn blue weakly and slowly 4 The tubes comprising the pore surface the hymenium are 9 15 mm deep yellow to olivaceous yellow mustard yellow turning dingy blue when bruised The pores are small 2 to 3 per mm circular and until old age a deep red color that eventually becomes paler The pore surface is often beaded with yellowish droplets when young a distinguishing characteristic and readily stains blue when bruised The stipe is 4 to 12 cm 1 6 to 4 7 in long and 1 to 2 5 cm 0 4 to 1 0 in thick at its apex It is roughly equal in thickness throughout its length though it may taper somewhat toward the top some specimens may appear ventricose swollen in the middle 18 The stipe surface is mostly red or yellowish near the base it is reticulate characterized by ridges arranged in the form of a net like pattern 18 Mycelia visible at the base of the stipe are yellowish white to light yellow 4 nbsp Young fruit bodies may secrete an amber liquid The spore print of B frostii is olive brown 18 The spores are thick walled smooth and spindle shaped with dimensions of 11 15 by 4 5 µm Longer spores up to 18 µm long may also be present 18 The cap cuticle or pileipellis is made of a tangled layer of gelatinized hyphae that are 3 6 µm wide 20 The spore bearing cells the basidia are four spored and measure 26 35 by 10 5 11 5 µm Cystidia are non fertile cells interspersed among the basidia and they are prevalent in the hymenial tissue of E frostii These hyaline translucent cells measure 30 53 long by 7 5 14 µm wide and range in shape from somewhat like a spindle tapering at each end but with one end typically rounded to subampullaceous shaped somewhat like a swollen bottle 4 Edibility and nutritional composition edit This species is nonpoisonous 21 Murrill wrote in 1910 of its edibility Usually viewed with suspicion because of its red hymenium but its properties are not accurately known 22 Since then several authors have advised against consuming the species due to its resemblance to other toxic red capped boletes 16 18 23 In his 100 Edible Mushrooms 2007 Michael Kuo notes that although the mushroom is apparently edible for some it affects others negatively 24 David Arora mentions that it is commonly sold in rural markets in Mexico 17 a 1997 study suggests that it is only consumed in rural areas in Queretaro state 25 Its taste and odor have been described as pleasant 16 or sweet 21 and somewhat like citrus 19 although the cuticle of the cap may taste acidic 18 Chemical analysis of fresh fruit bodies collected in Mexico showed them to have the following composition moisture 94 53 ash 0 323 dietary fiber 3 024 fat 0 368 and protein 1 581 The free fatty acid content of dried fruit bodies was 4 5 slightly more than the common button mushroom Agaricus bisporus which had 3 5 The majority of this total was oleic acid 1 95 followed by linoleic acid 1 68 and palmitic acid 1 69 25 Similar species edit nbsp Poisonous Boletus flammans is similar in appearance Other red capped boletes include the poisonous B flammans and B rubroflammeus the former grows most commonly under conifers the latter in association with hardwoods in eastern North America and southern Arizona 17 Often confused with Exsudoporus floridanus and E permagnificus but the latter species is known only from Europe and Western Asia and always grow in association with oaks and occasionally also with sweet chestnut 26 27 15 Exsudoporus floridanus differs from E frostii in having a lighter cap color and in the texture of the cap surface it is tomentose covered with dense short soft matted hairs or velutinous like velvet compared to the relatively smooth surface of E frostii Singer notes that although the physical characteristics between the two taxa may be blurred and are hard to define the area of origin can reliably distinguish them E floridanus is found on shaded lawns and scrubland in open oak stands in non tropical regions of Florida typically on grassy or sandy soil where it fruits between May and October 4 The fruit bodies of young specimens of B kermesinus newly described from Japan in 2011 are similar in appearance to E frostii In addition to its distribution B kermesinus can be distinguished from E frostii by having flesh that does not bruise blue and a stipe in which the reticulum is not as deep and coarse 28 B pseudofrostii found in Belize produces smaller caps that are 1 7 to 2 0 cm 0 7 to 0 8 in in diameter 29 Boletus russelli found in eastern North America has a red to reddish brown cap and reticulate stipe but its pore surface is yellow and the fruit body does not bruise blue 24 Ecology habitat and distribution edit nbsp Immature specimen with cap not fully expanded bruising is evident on the stipe Exsudoporus frostii is a mycorrhizal species 30 meaning that the fungus forms associations with the roots of various species of trees These associations are mutualistic because the fungus absorbs mineral nutrients from the soil and channels these into the plant while the plant provides the fungus with sugars a product of photosynthesis The characteristic feature of the mycorrhiza is the presence of a sheath of fungal tissue that encases the terminal nutrient absorbing rootlets of the host plant The fungus forms an extensive underground network of hyphae that radiate outward from the surface of the root sheath effectively increasing the surface area for nutrient absorption The hyphae also invade between the root cortical cells to form a Hartig net 31 Using pure culture techniques Exsudoporus frostii has been shown to form mycorrhizae with Virginia pine Pinus virginiana 30 while a field study confirms a similar association with the oak Quercus laurina 32 The fruit bodies grow solitarily scattered or in groups on the ground under hardwood trees the fungus fruits in summer to early autumn William Murrill noted its preference for growing in thin oak woods where the light is sufficient to enable grass to grow 7 and Alexander H Smith mentioned its preference for growing in thin sandy soil under scrub oak 3 In the United States it is distributed from Maine south to Georgia extending west to Tennessee and Michigan and in southern Arizona 4 19 In Mexico it is often found under Madrone 17 It has also been collected in Costa Rica where it associates with the oak species Quercus copeyensis Q costaricensis Q rapurahuensis and Q seemanii 33 A 1980 publication tentatively suggested that the fungus was also present in Italy 34 but the author later determined that the putative E frostii was actually Boletus siculus 27 Fruit bodies can be parasitized by the mold like fungus Sepedonium ampullosporum 35 Infection results in necrosis of the mushroom tissue and a yellow color caused by the formation of large amounts of pigmented aleurioconidia single celled conidia produced by extrusion from the conidiophores 36 See also edit nbsp Fungi portalList of North American boletesReferences edit a b Boletus frostii J L Russell MycoBank International Mycological Association Retrieved 2011 06 21 Frost CC 1874 Catalogue of Boleti of New England with descriptions of new species Bulletin of the Buffalo Society of Natural Sciences 2 100 5 a b Weber NS Smith AH 1980 The Mushroom Hunter s Field Guide Ann Arbor Michigan University of Michigan Press pp 104 5 ISBN 0 472 85610 3 a b c d e f g h Singer R 1947 The Boletoideae of Florida with notes on extralimital species III American Midland Naturalist 37 1 77 8 doi 10 2307 2421647 JSTOR 2421647 Dodge BO 1952 The fungi come into their own Mycologia 44 3 273 91 doi 10 1080 00275514 1952 12024197 JSTOR 4547605 Halling RE 1983 Boletes described by Charles C Frost Mycologia 75 1 70 92 doi 10 2307 3792925 JSTOR 3792925 a b Murrill WA 1909 The Boletaceae of North America Mycologia 1 1 4 18 doi 10 2307 3753167 JSTOR 3753167 Kirk PM Cannon PF Minter DW Stalpers JA 2008 Dictionary of the Fungi 10th ed Wallingford UK CAB International pp 672 709 ISBN 978 0 85199 826 8 Singer R 1945 New Boletaceae from Florida a preliminary communication Mycologia 37 6 797 9 doi 10 2307 3755143 JSTOR 3755143 Nuhn ME Binder M Taylor AFS Halling RE Hibbett DS 2013 Phylogenetic overview of the Boletineae Fungal Biology 117 7 8 479 511 doi 10 1016 j funbio 2013 04 008 PMID 23931115 Wu G Feng B Xu J Zhu X T Li Y C Zeng N K Hosen MI Yang ZL 2014 Molecular phylogenetic analyses redefine seven major clades and reveal 22 new generic clades in the fungal family Boletaceae Fungal Diversity 69 1 93 115 doi 10 1007 s13225 014 0283 8 S2CID 15652037 Vizzini A August 22 2014 Nomenclatural novelties PDF Index Fungorum 183 1 Wu Gang Li Yan Chun Zhu Xue Tai Zhao Kuan Han Li Hong Cui Yang Yang Li Fang Xu Jian Ping Yang Zhu L November 2016 One hundred noteworthy boletes from China Fungal Diversity 81 1 25 188 doi 10 1007 s13225 016 0375 8 ISSN 1560 2745 S2CID 22506275 Loizides M Bellanger JM Assyov B Moreau PA Richard F 2019 Present status and future of boletoid fungi Boletaceae on the island of Cyprus cryptic and threatened diversity unraveled by 10 year study Fungal Ecology 41 13 65 81 doi 10 1016 j funeco 2019 03 008 S2CID 181958289 a b Biketova AY Gelardi M Smith ME Simonini G Healy RA Taneyama Y Vasquez G Kovacs A Nagy LG Wasser SP Peintner U Nevo E Bunyard BA Vizzini A 2022 Reappraisal of the Genus Exsudoporus Boletaceae Worldwide Based on Multi Gene Phylogeny Morphology and Biogeography and Insights on Amoenoboletus Journal of Fungi 8 2 2 25 doi 10 3390 jof8020101 PMC 8874676 PMID 35205856 a b c Phillips R Boletus frostii Rogers Plants Archived from the original on 2012 02 18 Retrieved 2012 03 01 a b c d Arora D 1986 Mushrooms Demystified A Comprehensive Guide to the Fleshy Fungi Berkeley California Ten Speed Press p 529 ISBN 0 89815 169 4 a b c d e f g h i Thiers HD Smith AH 1971 The Boletes of Michigan Ann Arbor Michigan University of Michigan Press pp 343 4 ISBN 0 472 85590 5 a b c Bessette AE Roody WC Bessette AR 2000 Boletes of North America Syracuse New York Syracuse University Press p 114 ISBN 978 0 8156 0588 1 Kuo M January 2007 Boletus frostii MushroomExpert Com Retrieved 2012 03 01 a b Miller HR Miller OK 2006 North American Mushrooms A Field Guide to Edible and Inedible Fungi Guilford Connecticut FalconGuide p 385 ISBN 978 0 7627 3109 1 Murrill WA 1910 Poisonous mushrooms Mycologia 2 6 255 64 doi 10 2307 3753292 JSTOR 3753292 Bessette A Miller OK Jr Bessette AR Miller HR 1995 Mushrooms of North America in Color A Field Guide Companion to Seldom Illustrated Fungi Syracuse New York Syracuse University Press p 385 ISBN 0 8156 2666 5 a b Kuo M 2007 100 Edible Mushrooms Ann Arbor Michigan The University of Michigan Press pp 121 2 ISBN 978 0 472 03126 9 a b Leon Guzman MF Silva I Lopez MG 1997 Proximate chemical composition free amino acid contents and free fatty acid contents of some wild edible mushrooms from Queretaro Mexico Journal of Agricultural and Food Chemistry 45 11 4329 32 doi 10 1021 jf970640u Poder R 1981 Boletus permagnificus spec nov ein auffallender Rohrling der Sektion Luridi Fr assoziiert mit Eichen Boletus permagnificus new species a striking bolete of the section Luridi associated with oak Sydowia in German 34 149 56 ISSN 0082 0598 a b Alessio CL 1981 Boletus siculus inzenga il gia presunto B frostii Russell rinvenuto in Italia Boletus siculus is the supposed Boletus frostii discovered in Italy Micologia Italiana in Italian 10 2 40 2 Takahashi H Taneyama Y Koyama A 2011 Boletus kermesinus a new species of Boletus section Luridi from central Honshu Japan Mycoscience 52 6 419 24 doi 10 1007 s10267 011 0119 2 S2CID 83544311 Ortiz Santana B Lodge DJ Baroni TJ Both EE 2007 Boletes from Belize and the Dominican Republic PDF Fungal Diversity 27 2 247 416 see p 322 a b Vozzo JA Hackskaylo E 1961 Mycorrhizal fungi on Pinus virginiana Mycologia 53 5 538 9 doi 10 2307 3756310 JSTOR 3756310 Deacon J 2005 Fungal Biology Cambridge Massachusetts Blackwell Publishers pp 262 3 ISBN 1 4051 3066 0 Morris MH Perez Perez MA Smith ME Bledsoe CS 2009 Influence of host species on ectomycorrhizal communities associated with two co occurring oaks Quercus spp in a tropical cloud forest FEMS Microbiology Ecology 69 2 274 87 doi 10 1111 j 1574 6941 2009 00704 x PMID 19508503 Halling RE Muller GM Boletus frostii Macrofungi of Costa Rica New York Botanical Garden Retrieved 2011 09 29 Alessio CL 1980 Boletus Frostii presente in Italia Boletus frostii present in Italy Micologia Italiana in Italian 9 3 15 20 ISSN 0390 0460 Sahr T Ammer H Besl H Fischer M 1999 Infrageneric classification of the boleticolous genus Sepedonium species delimitation and phylogenetic relationships Mycologia 91 6 935 43 doi 10 2307 3761625 JSTOR 3761625 Archived from the original on 2015 09 23 Retrieved 2011 06 21 Neuhof T Berg A Besl H Schweche T Dieckmann R von Dohren H 2007 Peptaibol production by Sepedonium strains parasitizing Boletales Chemistry amp Biodiversity 4 6 1103 15 doi 10 1002 cbdv 200790099 PMID 17589879 S2CID 40865857 External links edit nbsp Wikimedia Commons has media related to Butyriboletus frostii nbsp Wikispecies has information related to Exsudoporus frostii Mushroom Observer Photographs Retrieved from https en wikipedia org w index php title Exsudoporus frostii amp oldid 1194765765, wikipedia, wiki, book, books, library,

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