Imleria badia

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Imleria badia
Boletus badius JPG1.jpg
I. badia under beech and oak
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Fungi
Division: Basidiomycota
Class: Agaricomycetes
Order: Boletales
Family: Boletaceae
Genus: Imleria
Species:
I. badia
Binomial name
Imleria badia
(Fr.) Vizzini (2014)
Synonyms [1]
  • Boletus castaneus ß badiusFr. (1818)
  • Boletus castaneus var. badius(Fr.) Fr. (1828)
  • Boletus badius(Fr.) Fr. (1832)
  • Rostkovites badia(Fr.) P.Karst. (1881)
  • Viscipellis badia(Fr.) Quél. (1886)
  • Ixocomus badius(Fr.) Quél. (1888)
  • Suillus badius(Fr.) Kuntze (1898)
  • Xerocomus badius(Fr.) E.-J.Gilbert (1931)
Imleria badia
Information icon.svg
Pores icon.pngPores on hymenium
Convex cap icon.svg Cap is convex
Adnate gills icon2.svg Hymenium is adnate
Bare stipe icon.svg Stipe is bare
Transparent spore print icon.svg
Transparent spore print icon.svg
 Spore print is olive to olive-brown
Mycorrhizal fungus.svgEcology is mycorrhizal
Mycomorphbox Choice.pngEdibility is choice

Imleria badia, commonly known as the bay bolete, is an edible, pored mushroom found in Eurasia and North America, where it grows in coniferous or mixed woods on the ground or on decaying tree stumps, sometimes in prolific numbers. Both the common and scientific names refer to the bay- or chestnut-coloured cap, which is almost spherical in young specimens before broadening and flattening out to a diameter up to 15 cm (6 in). On the cap underside are small yellowish pores that turn dull blue-grey when bruised. The smooth, cylindrical stipe, measuring 4–9 cm (1+1⁄2–3+1⁄2 in) long by 1–2 cm (1⁄2–3⁄4 in) thick, is coloured like the cap, but paler. Some varieties have been described from eastern North America, differing from the main type in both macroscopic and microscopic morphology.

Contents

First described scientifically by Elias Fries in 1818, the bay bolete was reclassified as Xerocomus badius in 1931, and it is still listed thus in several sources. Modern molecular phylogenetic studies show Xerocomus to be polyphyletic (not descended from the same common ancestor), and the bay bolete is not particularly closely related to species in that genus. Often considered a poor relation of the cep ( Boletus edulis ), I. badia is nevertheless regarded as a choice edible mushroom by some authors, such as food expert Antonio Carluccio, and is sold in markets in Europe and central Mexico. Its mushrooms are less often infested by maggots than other boletes. Several European studies have demonstrated that the mushroom can bioaccumulate some trace metals from the soil, such as mercury, cobalt, and nickel. Additionally, the mushroom contains a pigment that concentrates radioactive caesium; specimens collected in Europe following the 1986 Chernobyl disaster contained several times more caesium-137 than those collected before the incident.

Taxonomy

The bay bolete was first named as Boletus castaneus ß badius (i.e. a subspecies of Boletus castaneus ) by Elias Magnus Fries in 1818. [nb 1] Fries later renamed it as a variety of Boletus castaneus in 1828, [2] before assigning it distinct species status in his 1832 work Elenchus Fungorum. [3] The fungus has been transferred to several genera in its taxonomic history: Rostkovites by Petter Karsten in 1881; [4] Viscipellis and Ixocomus by Lucien Quélet in 1886 and 1888, respectively; [5] [6] and Suillus by Otto Kuntze in 1898. [7] In 1931, Edouard-Jean Gilbert reclassified it in the genus Xerocomus , [8] and many sources still list it thus. [9] Review of Xerocomus strongly suggested it was polyphyletic, and the genus was not accepted by some mycologists. The stickiness of its wet cap distinguishes the species from others classified in Xerocomus, and hence it was left in Boletus until Alfredo Vizzini placed it in its own genus in 2014. [10] [11] Genetic analysis published in 2013 shows that Imleria badia is related to B. pallidus and B. glabellus ; the three species form a clade known informally as the badius clade within a larger group (informally called anaxoboletus) in the suborder Boletineae. Other clades within the group include the Tylopilus , porcini (= Boletus sensu stricto) and Strobilomyces clades, as well as two other groups composed of members of various genera including Xerocomus (the taxa designated as Xerocomus species in this clade are not Xerocomus species and require new taxonomic designations) and Xerocomellus . [12]

Both the common and scientific names refer to the bay cap colour. Xerocomus badius 2008.JPG
Both the common and scientific names refer to the bay cap colour.

The species Boletus limatulus, originally published by Charles Christopher Frost in 1874, [13] was later redescribed, "with a slight tinge of irritation at the time, energy and gasoline spent", as a variety of I. badia by Wally Snell in 1945 (as Xerocomus badius var. limatulus). [14] The taxon name comes from the Latin limatulus, "rather polished" or "refined". [15] Varieties glaber and macrostipitatus were described from Nova Scotia, Canada, in 1976. [16]

The starting date of fungal taxonomy had been set as January 1, 1821, to coincide with the date of the works of Swedish naturalist Elias Magnus Fries, the "father of mycology". Rolf Singer argued that setting the starting date earlier to Christiaan Persoon's 1801 publication of Synopsis would make a name change necessary, as he had originally given what is now known as Royoporus badius the combination Boletus badius Pers. and if the bay bolete was classified in the genus Boletus, the name would be unavailable and the names Boletus glutinosus Krombh. or B. spadiceus Krombh. (non Fr.) would have to be used instead. [17]

The species name is the Latin adjective badia, meaning "chestnut brown". [18] The common name is likewise derived from the colour of the cap, likened to the coat of a bay horse. Alternate common names of a similar derivation include bay-brown bolete and bay-capped bolete, [19] and it is known as bolet bai in French. [20] It is also known as the false cep. [19] Variety glaber was named for its smooth (Latin: glaber, "without hairs") stipe, and macrostipitatus for its large (Latin: macro, "large") stipe. [16]

Description

With wet and sticky cap Kastanjeboleet.JPG
With wet and sticky cap
The pore surface stains bluish-grey when injured. 2007-07-14 Imleria badia 2.jpg
The pore surface stains bluish-grey when injured.

Imleria badia fruit bodies have a chestnut to dark brown cap, which is almost spherical in young specimens before broadening and flattening out to a diameter of up to 15 cm (6 in). The cap margin is acute, and cap surface velvety when young and slightly sticky when wet or old. [20] The cap cuticle is difficult to separate from the flesh underneath. [21] On the cap undersurface, the pores are initially cream to pale yellow, but become greenish yellow or olive with age. They stain dull blue to bluish-grey when bruised or cut, and are easily removed from the flesh. [20] The pores are initially circular, becoming more angular with age, [22] and number about one or two per millimetre. The tubes are 0.8–1.5 cm (3⁄8–5⁄8 in) long, [23] and are adnate to depressed around the area of attachment to the stipe. [24]

The flesh is mostly whitish or yellowish in some places; underneath the cap cuticle, it is brownish-pink or reddish brown. [25] Initially firm, it begins to soften under the cap in older mushrooms. [19] In some parts of the cap, such as the junction of the cap and the stipe, [21] the flesh stains pale blue when injured or exposed to air, particularly in damp weather. [19] This change is sometimes faint, [20] and not persistent, as it eventually reverts to its original colour. [21] The stipe is 4–9 cm (1+1⁄2–3+1⁄2 in) long by 1–2 cm (1⁄2–3⁄4 in) thick, and is similar in colour to the cap but paler, and sometimes with a rose-coloured tinge. [23] Its surface has faint longitudinal ridges, a fine powdering, [16] and fine reticulations (a net-like pattern of ridges) at the apex. [24] It often has a whitish region at the base [23] and the top, [21] and white mycelium at the base. [16] Unlike the bulbous stipe of many other boletes, the stipe of B. badius remains relatively slim and cylindrical. [26] The flesh of the stipe gets tougher with age. [19] Its smell has been described as fruity. [20]

The spore print is olive to olive-brown. [24] The smooth spores are somewhat oblong to slightly ventricose (fattened in the middle), and measure 10–14 by 4–5 µm. [23] The basidia (spore-bearing cells) are four-spored and measure 25–35 by 8–10 µm. Pleurocystidia (cystidia found on the faces of the tubes) are fuse-shaped and ventricose, with dimensions of 50–60 by 10–14 µm. [22]

Variety B. b. macrostipitatus differs from the main form by its grey-orange cap, shorter stipe measuring 5–7 cm (2–3 in), longer spores (15–18 by 4–5 µm), and longer pleurocystidia (30–55 by 10–14 µm). [23] The variety B. b. glaber has a smooth (glabrous) stipe, and smaller pleurocystidia (35–40 by 10–15 µm) and cheilocystidia (25–30 by 9–12 µm). [16]

Several chemical tests can be used to help identify the mushroom. A drop of ammonium hydroxide solution turns the cap cuticle a greenish to bluish colour. Application of iron(II) sulphate solution causes the flesh to stain a dull bluish-green, while the pores turn golden brown with a drop of dilute potassium hydroxide. [23]

Similar species

The similar colouration may cause confusion with Boletus projectellus , but the latter species is usually more robust, and has a reticulated stipe. Additionally, B. projectellus has the largest spores in the Boletaceae, up to about 30 µm in diameter. Another lookalike is Austroboletus gracilis , but this species does not have a blue bruising reaction, and its pore surface is initially white before turning pinkish. [27] Compared to I. badia, B. subtomentosus fruit bodies have narrower stipes, paler brown, dry caps, [28] and wider pores that do not stain blue on bruising. This latter species is not as good to eat. [19] In western North America, I. badia is replaced by the similar B. zelleri , which also grows both on the ground and on rotten wood. [29] The European species Xerocomus bubalinus can be mistaken for I. badia, but it has a paler yellow-brown cap flushed with pinkish-red, and is not sticky when wet. [30]

Ecology, distribution and habitat

The mushrooms often appear in huge numbers, allowing for large collections. Boletus badius 5052175998 df099ccc79 b cropped.jpg
The mushrooms often appear in huge numbers, allowing for large collections.

Although the bay bolete is predominantly a mycorrhizal species, it does have some saprophytic tendencies and may be able to use this lifestyle in certain circumstances. [21] The ectomycorrhizae formed between I. badia and spruce (Picea abies) have active hyphal sheaths and a higher potential to store nitrogen, phosphorus, potassium, magnesium, iron, and zinc than other mycorrhizal types, indicating the fungus is well adapted to acidic stands and its mycorrhizae are very efficient in uptake and storage of macronutrients. [31] Mycorrhizae with Monterey pine (Pinus radiata) have also been described. [32]

The bay bolete is common in coniferous and less commonly mixed woodlands in Europe, from the British Isles, where it is abundant throughout from August to November, [33] east to the Black Sea Region in Turkey. [34] In Asia, the species has been recorded from Jordan [35] mainland China, [36] and Taiwan. [22] The North American distribution extends from eastern Canada west to Minnesota and south to North Carolina, where the mushroom fruits from July to November. [37] It also grows in central Mexico. [38] The variety B. b. macrostipitatus is found from eastern Canada south to Maine and New York state, [23] while variety B. b. glaber is known from the Atlantic Maritime Ecozone of eastern Canada. [39] Fruit bodies appear singly or scattered on the ground, or on decaying tree stumps, and can be well hidden by pine needles and ferns. Fruiting tends to peak three or four days after rain during warm weather. [40] They can be prolific, especially in highland areas that are humid and shady. [21] It is commonly found under white pine, spruce, and hemlock, [25] and also occurs under deciduous trees, especially beech. [21] It can also occur in grassy or mossy areas at or near forest margins; [20] Italian restaurateur and cook Antonio Carluccio recalled picking them in the grounds of Blenheim Palace. [40] It does not occur on calcareous (chalky) soils. [26]

I. badia fruit bodies are less affected by insects than other boletes. [27] Orbatid mites such as Carabodes femoralis , Nothrus silvestris and Oribatula tibialis eat them, [41] as do squirrels. [40] Several microbial pathogens can damage the fruit bodies, and have had an effect on populations in China, including soft rot caused by Pseudomonas aeruginosa , and black mould caused by Mucor , Sepedonium , Paecilomyces , and Diasporangium species. [36]

Uses

Dried in Poland Dried mushrooms. Poland.JPG
Dried in Poland

Often considered a poor relation of the cep ( Boletus edulis ), the bay bolete is nevertheless highly regarded as a choice edible mushroom by some authors such as Carluccio. In central Mexico, it is collected from Izta-Popo Zoquiapan National Park and sold in neighbouring markets. [38] It may cause an allergic reaction in some people, [42] and the blue discolouration upon bruising can be offputting, [40] although the staining disappears from white flesh when it is cooked. [43] The flavour is milder than its better-known relative. Younger specimens are best for eating, though more mature ones can be suitable for cutting up and drying. The tendency for the pores to absorb water means that wiping rather than washing is recommended before use in the kitchen. [40] Unlike most boletes, I. badia can be eaten raw (though only young mushrooms should be used). Otherwise it can be fried in butter, or used with meat or fish recipes. Mushrooms can also be frozen, dried, [40] or pickled in cider vinegar, wine, or extra virgin olive oil, [44] and later used in sauces or soups. [40]

The fruit bodies can be used to make mushroom dyes. Depending on the mordant used, colours ranging from yellow, orange, gold, and green-brown can be obtained. Without mordant, a yellow colour is produced. [45]

Research

In laboratory experiments, extracts of I. badia fruit bodies have been shown to have significant antioxidative properties in vitro . [46] Fruit bodies contain the compound theanine, [47] an amino acid and a glutamic acid analogue found in green tea. [48] Efforts have been made to establish a protocol for producing theanine by growing the fungus mycelium using submerged fermentation. [49] Several indole compounds have been detected in fruit bodies. Unprocessed mushrooms contain tryptophan (0.68 mg per 100 g dry weight), tryptamine (0.47), serotonin (0.52), kynurenine sulphate (1.96), and kynurenic acid (1.57). Due to their temperature sensitivity, cooking significantly changes the contents and composition of indole compounds: cooked mushrooms contained tryptophan (1.74 mg/100 g dw), 5-methyltryptophan (6.55), melatonin (0.71), and indoleacetonitrile (2.07). [50] Fruit body extracts have been shown to slow the growth of certain tumour cell lines in cell culture. [48] [51]

Polish studies found that although the mushroom bioaccumulates mercury and cobalt from the soil, occasional consumption of mushrooms should not cause maximum allowable intake doses to be exceeded. [52] [53] Similar conclusions about safety were made in a Polish study of the mushroom's ability to accumulate organochlorine compounds. [54] Different methods of preparation for consumption affect the leaching rate of cadmium, lead, and mercury. [55] After the 1986 Chernobyl disaster, several studies showed I. badia bioaccumulates radioactive caesium, 137Cs. [56] 137Cs is produced in nuclear power plants following the chain decay of 235U to 137Te, and has a half-life of thirty years. A German study showed that mushrooms collected from 1986 to 1988 had radiocaesium contents that were 8.3 to 13.6 times greater than mushrooms collected before the accident in 1985. [57] This caesium-sequestering effect is caused by a brown pigment, the polyphenol compound norbadione A, which is related to a family of mushroom pigments known as pulvinic acids. [58] Norbadione A has been investigated for its ability to provide a protective effect against the damaging effects of ionizing radiation. Tests with cell cultures and mice show that although it has some protective effect, it is toxic to cells in higher doses. [59] A new series of alkali chelators based on the structure of norbadione A has been reported. [60] The mushroom may have potential as a bioremediation agent to clean up contaminated sites. [61]

See also

Notes

  1. ↑ Though he wrote, "forte distincta species; sed ex unico a me viso specimine distinguere potui, neque debui" (Perhaps a distinct species, but I could not state it definitely from the only specimen I have seen, nor should I.)

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<i>Chalciporus piperatus</i> Species of fungus in the family Boletaceae found in mixed woodland in Europe and North America

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<i>Xerocomellus chrysenteron</i> Species of fungus

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<i>Hortiboletus rubellus</i> Species of fungus

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<i>Xerocomus subtomentosus</i> Species of fungus

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<i>Exsudoporus frostii</i> Species of fungus in the family Boletaceae found in North America

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<i>Aureoboletus mirabilis</i> Species of fungus

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<i>Xerocomellus zelleri</i> Species of fungus

Xerocomellus zelleri, commonly known as Zeller's bolete, is an edible species of mushroom in the family Boletaceae. First described scientifically by American mycologist William Alphonso Murrill in 1912, the species has been juggled by various authors to several genera, including Boletus, Boletellus, and Xerocomus. Found solely in western North America from British Columbia south to Mexico, the fruit bodies are distinguished by their dark reddish brown to nearly black caps with uneven surfaces, the yellow pores on the underside of the caps, and the red-streaked yellow stems. The fungus grows in summer and autumn on the ground, often in Douglas fir forests or on their margins. The development of the fruit bodies is gymnocarpic, meaning that the hymenium appears and develops to maturity in an exposed state, not enclosed by any protective membrane.

<i>Suillellus amygdalinus</i> Species of fungus

Suillellus amygdalinus is a fungus of the bolete family found in western North America. The fruit bodies, or mushrooms, are characterized by their thick, red to brown caps, red pores, and the strong bluing reaction observed when the mushroom tissue is injured or cut. The cap can reach diameters of up to 12 cm (4.7 in) and the stipe 9 cm (3.5 in) long by 3 cm (1.2 in) thick at maturity. This mushroom has been found in manzanita and madrone woodlands of central California north to southern Oregon. Although the edibility of the mushroom is not known with certainty, it may be poisonous, and is not recommended for consumption. Other similar red-pored, bluing boletes from North America, including Rubroboletus eastwoodiae, Boletus luridiformis, and B. subvelutipes, can be distinguished from S. amygdalinus either by the color of the cap, the degree of reticulation on the stipe, or by location.

<i>Xerocomus illudens</i> Species of fungus

Xerocomus illudens is a species of bolete fungus in the family Boletaceae. Described as new to science in 1898, it is found in Asia and North America, where it grows in a mycorrhizal association with oak.

<i>Xerocomellus</i> Genus of fungi

Xerocomellus is a genus of fungi in the family Boletaceae. The genus, as it was described in 2008, contained 12 species. However X. rubellus and X. engelii were transferred to the new genus Hortiboletus and X. armeniacus was transferred to the new genus Rheubarbariboletus in 2015. Molecular analysis supports the distinction of Xerocomellus species from Boletus and Xerocomus, within which these species were formerly contained. Xerocomellus in fact is only distantly related to Xerocomus and is most closely related to Tylopilus, Boletus sensu stricto, Porphyrellus, Strobilomyces, and Xanthoconium.

<i>Harrya chromapes</i> Species of fungus

Harrya chromapes, commonly known as the yellowfoot bolete or the chrome-footed bolete, is a species of bolete fungus in the family Boletaceae. The bolete is found in eastern North America, Costa Rica, and eastern Asia, where it grows on the ground, in a mycorrhizal association with deciduous and coniferous trees. Fruit bodies have smooth, rose-pink caps that are initially convex before flattening out. The pores on the cap undersurface are white, aging to a pale pink as the spores mature. The thick stipe has fine pink or reddish dots (scabers), and is white to pinkish but with a bright yellow base. The mushrooms are edible but are popular with insects, and so they are often infested with maggots.

<i>Boletus subluridellus</i> Species of fungus

Boletus subluridellus is a species of bolete fungus in the family Boletaceae. Described as new to science in 1971 by American mycologists, the bolete is found in the eastern United States and Canada. It grows on the ground in coniferous and mixed forests in a mycorrhizal association with deciduous trees, especially oak. The fruit bodies (mushrooms) have orangish-red, broadly convex caps that are up to 10 cm (3.9 in) in diameter, with small, dark reddish pores on the underside. The pale yellow stipe measures 4–9 cm (1.6–3.5 in) long by 1.5–2.3 cm (0.6–0.9 in) thick. All parts of the fruit body will quickly stain blue when injured or touched.

<i>Sutorius eximius</i> Species of fungus

Sutorius eximius, commonly known as the lilac-brown bolete, is a species of fungus in the family Boletaceae. This bolete produces fruit bodies that are dark purple to chocolate brown in color with a smooth cap, a finely scaly stipe, and a reddish-brown spore print. The tiny pores on the cap underside are chocolate to violet brown. It is widely distributed, having been recorded on North America, South America, and Asia, where it grows in a mycorrhizal relationship with both coniferous and deciduous trees.

References

  1. ↑ "Synonymy: Boletus badius (Fr.) Fr., Syst. mycol., Index alphab. (Lundae): 56 (1832)". Index Fungorum. CAB International. Retrieved 2013-07-12.
  2. ↑ Fries EM (1828). Elenchus Fungorum (in Latin). Vol. 1. Greifswald: Ernestus Mauritius. p. 126.
  3. ↑ Fries EM (1821). Systema Mycologicum (in Latin). Vol. 1. Lundin: Ex Officina Berlingiana. p. 392.
  4. ↑ Karsten P. (1881). "Enumeratio Boletinearum et Polyporearum Fennicarum, systemate novo dispositarum". Revue Mycologique Toulouse (in Latin). 3 (9): 16–19.
  5. ↑ Quélet L. (1886). Enchiridion Fungorum in Europa media et praesertim in Gallia Vigentium (in Latin). Lutetia: Octave Dion. p. 156.
  6. ↑ Quélet L. (1888). Flore mycologique de la France et des pays limitrophes (in French). Paris: Octave Doin. p. 412.
  7. ↑ Kuntze, O. (1898). Revisio generum plantarum (in German). Vol. 3. Leipzig: A. Felix. p. 535.
  8. ↑ Gilbert E-J (1931). Les Livres du Mycologue. Tome III: Les Bolets (in French). Paris: E. Le François. p. 92.
  9. ↑ Noordeloos ME (2007). "Hoe raak ik thuis in de boleten – 7. De fluweelboleten (Xerocomus) van Nederland" [The genus Xerocomus in the Netherlands](PDF). Coolia (in Dutch). 50 (1): 1–20.
  10. ↑ Šutara J. (2008). "Xerocomus s. l. in the light of the present state of knowledge" (PDF). Czech Mycology. 60 (1): 29–62. doi:10.33585/cmy.60104.
  11. ↑ Vizzini A. (12 June 2014). "Nomenclatural novelties" (PDF). Index Fungorum (147): 1. ISSN   2049-2375.
  12. ↑ 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.
  13. ↑ Frost CC (1874). "Catalogue of boleti of New England, with descriptions of new species". Bulletin of the Buffalo Society of Natural Sciences. 2: 100–05.
  14. ↑ Snell WH (1945). "Notes on boletes: VII". Mycologia. 37 (3): 374–88 (see pp. 382–83). doi:10.2307/3754872. JSTOR   3754872.
  15. ↑ Simpson DP (1979) [1854]. Cassell's Latin Dictionary (5th ed.). London: Cassell. p. 346. ISBN   978-0-304-52257-6.
  16. 1 2 3 4 5 Grund DW, Harrison KA (1976). Nova Scotian Boletes. Bibliotheca Mycologia. Vol. 47. Lehre: J. Cramer. pp. 116, 118. ISBN   978-3-7682-1062-1.
  17. ↑ Singer R. (1960). "Persoon's Synopsis 1801 as starting point for all fungi?". Taxon. 9 (2): 35–37. doi:10.2307/1217835. JSTOR   1217835.
  18. ↑ Nilson S, Persson O (1977). Fungi of Northern Europe 1: Larger Fungi (Excluding Gill-Fungi). Harmondsworth: Penguin. p. 108. ISBN   978-0-14-063005-3.
  19. 1 2 3 4 5 6 Lamaison J-L, Polese J-M (2005). The Great Encyclopedia of Mushrooms. Cologne: Könemann. p. 26. ISBN   978-3-8331-1239-3.
  20. 1 2 3 4 5 6 Zeitlmayr L. (1976). Wild Mushrooms: An Illustrated Handbook. Hertfordshire: Garden City Press. pp. 98–99. ISBN   978-0-584-10324-3.
  21. 1 2 3 4 5 6 7 Alessio CL (1985). Boletus Dill. ex L. (sensu lato) (in Italian). Saronno: Biella Giovanna. pp. 323–27.
  22. 1 2 3 Yeh K-W, Chen Z-C (1981). "The boletes of Taiwan (II)" (PDF). Taiwania. 26 (1): 100–15. doi:10.6165/tai.1981.26.100. ISSN   0372-333X. Archived from the original (PDF) on 2018-04-25. Retrieved 2018-12-10.
  23. 1 2 3 4 5 6 7 Bessette AR, Bessette A, Roody WC (2000). North American Boletes: A Color Guide to the Fleshy Pored Mushrooms. Syracuse: Syracuse University Press. pp. 96–97. ISBN   978-0-8156-0588-1.
  24. 1 2 3 Miller HR, Miller OK Jr (2006). North American Mushrooms: A Field Guide to Edible and Inedible Fungi. Guilford: Falcon Guides. p. 397. ISBN   978-0-7627-3109-1.
  25. 1 2 Snell W, Dick EA (1970). The Boleti of Northeastern North America. Lehre: J. Cramer. p. 55. ISBN   978-0-85486-016-6.
  26. 1 2 Haas H. (1969). The Young Specialist looks at Fungi. London: Burke. p. 42. ISBN   978-0-222-79409-3.
  27. 1 2 Roody WC (2003). Mushrooms of West Virginia and the Central Appalachians. Lexington: University Press of Kentucky. p. 315. ISBN   978-0-8131-9039-6.
  28. ↑ Roberts P, Evans S (2011). The Book of Fungi. Chicago: University of Chicago Press. p. 328. ISBN   978-0-226-72117-0.
  29. ↑ Arora D. (1986). Mushrooms Demystified: A Comprehensive Guide to the Fleshy Fungi. Berkeley: Ten Speed Press. p. 519. ISBN   978-0-89815-169-5.
  30. ↑ Hills AE (2008). "The genus Xerocomus: A personal view, with a key to the British species". Field Mycology. 9 (3): 77–96. doi: 10.1016/S1468-1641(10)60416-1 .
  31. ↑ Kottke I, Qian XM, Pritsch K, Haug I, Oberwinkler F (1998). "Xerocomus badius – Picea abies, an ectomycorrhiza of high activity and element storage capacity in acidic soil". Mycorrhiza. 7 (5): 267–75. doi:10.1007/s005720050191. PMID   24578053. S2CID   24196528.
  32. ↑ Duñabeitia MK, Hormilla S, Salcedo I, Peña JI (1996). "Ectomycorrhizae synthesized between Pinus radiata and eight fungi associated with Pinus spp". Mycologia. 88 (6): 897–908. doi:10.2307/3761052. JSTOR   3761052.
  33. ↑ Phillips R. (2006). Mushrooms. London: Pan MacMillan. pp. 276–77. ISBN   978-0-330-44237-4.
  34. ↑ Sesli E. (2007). "Preliminary checklist of macromycetes of the East and Middle Black Sea Regions of Turkey" (PDF). Mycotaxon. 99: 71–74.
  35. ↑ Natour RM, Salhab AS, El-Moumani AR, Saba EF (1992). "Wild mushroom in Jordan". Dirasat Series B Pure and Applied Sciences. 19 (2): 47–60.
  36. 1 2 Guo YH, Gui MY, Wang LX, Ye K (2004). "Investigation report on diseases of wild Xerocomus badius in Yunnan province of China". Edible Fungi of China (in Chinese). 23 (2): 48–51. ISSN   1003-8310.
  37. ↑ Phillips R. (2005). Mushrooms and Other Fungi of North America. Buffalo: Firefly Books. p. 260. ISBN   978-1-55407-115-9.
  38. 1 2 Dugan FM (2011). Conspectus of World Ethnomycology. St. Paul: American Phytopathological Society. p. 78. ISBN   978-0-89054-395-5.
  39. ↑ Malloch D. (2010). "Fleshy fungi (Basidiomycota) of the Atlantic Maritime Ecozone". In McAlpine DF, Smith IM (eds.). Assessment of Species Diversity in the Atlantic Maritime Ecozone. Ottawa: NRC Research Press. p. 121. ISBN   978-0-660-19835-4.
  40. 1 2 3 4 5 6 7 Carluccio A. (2003). The Complete Mushroom Book. London: Quadrille. pp. 33–34. ISBN   978-1-84400-040-1.
  41. ↑ Schneider K, Renker C, Maraun M (2005). "Oribatid mite (Acari, Oribatida) feeding on ectomycorrhizal fungi". Mycorrhiza. 16 (1): 67–72. doi:10.1007/s00572-005-0015-8. PMID   16133254. S2CID   7299733.
  42. ↑ Bennink A, de Vries B (2007). "Allergie voor boleten" [Allergic to boletes](PDF). Coolia (in Dutch). 50 (1): 47–48.
  43. ↑ Læssoe T. (2002). Mushrooms. Smithsonian Handbooks (2nd ed.). London: Dorling Kindersley Adult. p. 188. ISBN   978-0-7894-8986-9.
  44. ↑ Jordan P, Wheeler S (2000) [1995]. The Practical Mushroom Encyclopedia. London: Southwater. p. 40. ISBN   978-1-84215-243-0.
  45. ↑ Bessette A, Bessette AR (2001). The Rainbow Beneath my Feet: A Mushroom Dyer's Field Guide. Syracuse: Syracuse University Press. p. 36. ISBN   978-0-8156-0680-2.
  46. ↑ Haghi AK (2011). Food Science: Research and Technology. Toronto: CRC Press. p. 76. ISBN   978-1-926895-01-7.
  47. ↑ Casimir J, Jadot J, Renard M (1960). "Séparation et caractérisation de la N-éthyl-γ-glutamine à partir de Xerocomus badius" [Separation and characterization of N-ethyl-gamma-glutamine from Xerocomus badius]. Biochimica et Biophysica Acta (in French). 39 (3): 462–68. doi:10.1016/0006-3002(60)90199-2. PMID   13808157.
  48. 1 2 Rogers R. (2012). The Fungal Pharmacy: The Complete Guide to Medicinal Mushrooms and Lichens of North America. Berkeley: North Atlantic Books. p. 68. ISBN   978-1-58394-595-7.
  49. ↑ Li J, Li P, Liu F (2008). "Production of theanine by Xerocomus badius (mushroom) using submerged fermentation". LWT - Food Science and Technology. 41 (5): 883–99. doi:10.1016/j.lwt.2007.05.020.
  50. ↑ Muszyńska B, Sułkowska-Ziaja K (2012). "Analysis of indole compounds in edible Basidiomycota species after thermal processing". Food Chemistry. 132 (1): 455–59. doi:10.1016/j.foodchem.2011.11.021. PMID   26434315.
  51. ↑ Badalyan S. (2012). "Medicinal aspects of edible mycorrhizal mushrooms". In Zambonelli A, Bonito GM (eds.). Edible Ectomycorrhizal Mushrooms. Soil Biology. Vol. 34. Berlin: Springer-Verlag. pp. 317–34. ISBN   978-3-642-33822-9.
  52. ↑ Falandysz J, Kojta AK, Jarzyńska G, Drewnowska M, Dryżałowska A, Wydmańska D, Kowalewska I, Wacko A, Szlosowska M, Kannan K, Szefer P (2012). "Mercury in bay bolete (Xerocomus badius): Bioconcentration by fungus and assessment of element intake by humans eating fruiting bodies". Food Additives and Contaminants. 29 (6): 951–61. doi:10.1080/19440049.2012.662702. PMID   22416950. S2CID   5401125.
  53. ↑ Mleczek M, Siwulski M, Stuper-Szablewska K, Rissmann I, Sobieralski K, Goliński P (2013). "Accumulation of elements by edible mushroom species: Part I. Problem of trace element toxicity in mushrooms". Journal of Environmental Science and Health, Part B. 48 (1): 69–81. doi:10.1080/03601234.2012.716733. PMID   23030443. S2CID   21445417.
  54. ↑ Gałgowska M, Pietrzak-Fiećko R, Felkner-Poźniakowska B (2012). "Assessment of the chlorinated hydrocarbons residues contamination in edible mushrooms from the North-Eastern part of Poland". Food and Chemical Toxicology . 50 (11): 4125–29. doi:10.1016/j.fct.2012.07.039. PMID   22889896.
  55. ↑ Svoboda L, Kalac P, Spicka J, Janouskova D (2002). "Leaching of cadmium, lead and mercury from fresh and differently preserved edible mushroom, Xerocomus badius, during soaking and boiling". Food Chemistry. 79 (1): 41–45. doi:10.1016/S0308-8146(02)00175-9.
  56. ↑ Elstner EF, Fink R, Höll W, Lengfelder E, Ziegler H (1987). "Natural and Chernobyl-caused radioactivity in mushrooms, mosses and soil-samples of defined biotops in SW Bavaria". Oecologia. 73 (1): 553–58. Bibcode:1987Oecol..73..553E. doi:10.1007/bf00379415. JSTOR   4218406. PMID   28311973. S2CID   6354011.
  57. ↑ Paulus W, Reisinger A (1990). "Die Auswirkungen des Reaktorunfalls von Tschernobyl auf den Gehalt an radioaktivem Cäsium in den Fruchtkörpern der Mykorrhizapilzarten Lactarius rufus und Xerocomus badius im Fichtelgebirge" [The influence of the Chernobyl accident on radiocesium content in fruitbodies of the ectomycorrhizal fungi Lactarius rufus and Xerocomus badius collected in the Fichtelgebirge, East Germany](PDF). Zeitschrift für Mykologie (in German). 56 (2): 279–84. Archived from the original (PDF) on 2015-09-23. Retrieved 2013-07-07.
  58. ↑ Aumann DC, Clooth G, Steffan B, Steglich W (1989). "Complexation of cesium-137 by the cap pigments of the bay boletus (Xerocomus badius)". Angewandte Chemie International Edition in English. 28 (4): 453–54. doi:10.1002/anie.198904531.
  59. ↑ Le Roux A, Josset E, Benzina S, Nadal B, Desage-El Murr M, Heurtaux B, Taran F, Denis J-M, Le Gall T, Meunier S, Bischoff P (2012). "Evaluation of the radioprotective potential of the polyphenol norbadione A". Letters in Drug Design & Discovery. 9 (1): 48–53. doi:10.2174/157018012798192900.
  60. ↑ Korovitch A, Le Roux A, Barbault F, Hémadi M, Ha-Duong N-T, Lion C, Wagner A, El Hage Chahine J-M (2013). "A new series of Cs+, K+ and Na+ chelators: Synthesis, kinetics, thermodynamics and modeling". Inorganica Chimica Acta. 394: 45–57. doi:10.1016/j.ica.2012.08.009.
  61. ↑ Stamets P. (2011). Mycelium Running: How Mushrooms Can Help Save the World. Berkeley: Ten Speed Press. p. 105. ISBN   978-1-60774-124-4.
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