Inocybe_maculata

<i>Inosperma maculatum</i>

Inosperma maculatum

Species of fungus


Inosperma maculatum, formerly known as Inocybe maculata and commonly known as the frosty fibrecap or brown inocybe,[2] is a species of mushroom in the family Inocybaceae. First described by Jean Louis Émile Boudier in 1885, I. maculatum is found throughout Europe, Asia and North America. It is a medium-sized brown mushroom with a fibrous, brown cap with white remnants of a universal veil in the middle. The stem is cream or brown. The species is ectomycorrhizal and grows at the base of various trees, including beech. Inosperma maculatum is poisonous, containing muscarine. Possible symptoms after consumption of I. maculatum mushrooms are salivation, lacrimation, urination, defecation, gastrointestinal problems and vomiting, with the possibility of death due to respiratory failure.

Quick Facts Inosperma maculatum, Scientific classification ...
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Taxonomy, phylogeny, and naming

I. maculatum f. fulvum

I. maculatum

I. cookei

I. quietiodor

Phylogeny and relationships of I. maculata and related species in section Maculata based on ITS, large-subunit, and mitochondrial small-subunit rRNA sequence data.[3]

The species was given its specific epithet, "maculata" (from the Latin for "spotted"),[4] by Jean Louis Émile Boudier in 1885 in an article in the Bulletin de la Société Botanique de France.[5] Within the genus Inocybe, it was placed within the subgenus Inosperma and section Rimosae. However, Phylogenetic analysis, has shown that section Rimosae as formerly defined does not form a monophyletic group (that is, descended from a single exclusive ancestor), and former Rimosae species are better grouped into two clades, Maculata and Rimosae. Other species joining I. maculata in the Maculata clade include I. cookei, I. quietiodor, I. rhodiola, I. adaequata, and I. erubescens.[3] A 2019 multigene phylogenetic study by Matheny and colleagues found that I. maculata and its relatives in the subgenus Inosperma were only distantly related to the other members of the genus Inocybe. Inosperma was raised to genus rank and the species became Inosperma maculatum.[6]

There has been some debate about its status as a single species; due to the wide geographic and morphological variation of the species, some authors have proposed multiple species and varieties. In response, mycologist Thom Kuyper has listed over thirty specific names and varieties as synonyms of Inocybe lacera, which is still generally recognised.[3] It has also been suggested that Inocybe lanatodisca is a synonym, but where the species occur together, they can be distinguished from each other, and so it is still recognised as distinct.[7] The form I. maculata f. fulva was named and described in 1991 by Marcel Bon in France.[8] Inosperma maculatum is commonly known as the frosty fibrecap.[9]

Description

Caps flatten out in maturity and develop a broad umbo.
The crowded gills have a finely toothed edge and an adnate attachment to the stem.

Inosperma maculatum has a conical or bell-shaped cap which is up to 8 centimetres (3.1 in) in diameter. As the mushrooms age, the cap becomes flatter, and the broad umbo becomes prominent.[9] The centre of the cap has white remains of the universal veil,[9] especially on younger mushrooms.[10] The cap is covered in fibres which extend from the centre of the cap to the margin (which is usually split). The cap is typically a chestnut brown in colour, though it is paler towards the margin.[9] As well as chestnut, the camp has been described as "Buckthorn brown", "snuff brown", "tawny olive" and "Saccardo's umber".[7] Both cap colour and the presences of veil remnants are known to be very variable.[3] In appearance, Inosperma maculatum f. fulvum has a lighter cap colour (typically more yellow to reddish-brown) and less (or even no) remnants of the veil on the cap.[3] The gill attachment is adnate, meaning that the gills are attached to the stem along their entire depth. The gills are crowded, with white edges that are finely toothed. Younger mushrooms have gills that are greyish-white that eventually mature to an olive-brown colour. The stem is up to 8 cm (3.1 in) in length, and generally cylindrical in shape, though it is often thicker towards the base.[9] While the stem is initially solid, it later becomes hollow.[5] There is often a small bulb at the base of the stem. The stem has cream colouration, becoming gradually browner with age. The base sometimes white and powdery.[9] The flesh is white.[10]

Microscopic features

Inosperma maculatum has thin-walled cheilocystidia, which are clavate (club-shaped), lack encrustation at the apex,[10] and are colourless.[5] The basidia are also clavate, and can be two-, three- or four-spored, and measure from 15 to 30 micrometres (μm) by 5 to 9 μm.[5] The sterigmata (the narrow horns on the end of the basidia which hold the spores) are 4 to 5 μm long.[5] It lacks pleurocystidia.[5] The species leaves a snuff-brown spore print. The spores themselves are smooth and bean shaped;[10] they have a yellow-brown to rusty brown colouration,[5] and measure from 9 to 11 μm by 4.5 to 5.5 μm.[10] The hyphae can have clamp connections, but can also lack them.[5]

Similar species

Inosperma maculatum is similar to the variable Inocybe lacera, the split fibrecap, but it can be differentiated by the darker colouration of the cap, and the white remains of the veil in the centre of the cap.[9] The species is also similar in appearance to Inocybe lanatodisca, but can be readily distinguished by odour (I. lanatodisca has a characteristic sweet, green-corn smell) and the colour of the cap (I. lanatodisca has a fulvous cap).[7] It is closely related to Inocybe fastigiata, but can again be distinguished by colour; I. fastigiata has lighter coloured fibrils.[11]

Distribution and habitat

Inosperma maculatum is an ectomycorrhizal species,[12] with a wide ecological range.[3] It is found in all biomes from low-lying deciduous woodland to arctic-alpine areas.[3] It typically grows on the ground in deciduous (or mixed[5]) woodland, favouring beech. It grows best on chalky soil,[9][10] among leaf litter.[13] In North America, it favours sandy soil, clay or moss.[7] It is also encountered on pathsides.[13] As well as beech, the species has been recorded growing in association with hornbeam, hazel, oak and lime. Inocybe maculata f. fulva favours birch, spruce, pine, Populus, willow, (as well as Dryas and Polygonum in alpine regions).[3] Mushrooms grow individually or in scattered groups.[5] Though widespread in the areas it is found, it is not a common species.[9] It is found from western Europe to eastern Asia;[5][10][14] and in North America, from where it was first collected in the 1960s.[7] Inocybe maculata f. fulva was first identified in France, and has since been found elsewhere in Europe.[3]

Edibility

The flesh has a mild taste, and a strong, pungent, fruity smell.[10][13] The mushroom is poisonous,[10] containing muscarine compounds.[13] Consumption of the mushroom could lead to a number of physiological effects, including: salivation, lacrimation, urination, defecation, gastrointestinal problems and emesis (vomiting); this array of symptoms is also known by the acronym SLUDGE.[15] Other potential effects include a drop in blood pressure, sweating and death due to respiratory failure.[15]

See also


References

  1. Arora, David (1986). Mushrooms demystified: a comprehensive guide to the fleshy fungi (Second ed.). Berkeley: Ten Speed Press. pp. 458–459. ISBN 978-0-89815-169-5.
  2. Larsson, E.; Ryberg, M.; Moreau, P.-A.; Mathiesen, Å. Delcuse; Jacobsson, S. (2009). "Taxonomy and evolutionary relationships within species of section Rimosae (Inocybe) based on ITS, LSU and mtSSU sequence data" (PDF). Persoonia. 23: 86–98. doi:10.3767/003158509X475913. PMC 2802730. PMID 20198163. Archived from the original (PDF) on 27 July 2011. Retrieved 23 September 2010.
  3. Fowler, James Alexander; Brown, Paul Martin (2005). Wild Orchids of South Carolina. University of South Carolina Press. p. 36. ISBN 978-1-57003-566-1.
  4. Bi, Zhishu; Zheng, Guoyang; Li, Taihui (1993). The Macrofungus Flora of China's Guangdong Province. Chinese University Press. p. 429. ISBN 978-962-201-556-2.
  5. Matheny, P. Brandon; Hobbs, Alicia M.; Esteve-Raventós, Fernando (2020). "Genera of Inocybaceae: New skin for the old ceremony". Mycologia. 112 (1): 83–120. doi:10.1080/00275514.2019.1668906. PMID 31846596. S2CID 209407151.
  6. Grund, D. W.; Stuntz, D. E. (1968). "Nova Scotian Inocybes. I". Mycologia. 60 (2). Mycological Society of America: 406–25. doi:10.2307/3757170. ISSN 0027-5514. JSTOR 3757170.
  7. Bon, M. "Flore mycologique du littoral - 07". Documents Mycologiques. 21 (81): 47–54.
  8. Sterry, Paul; Hughes, Barry (2009). Complete Guide to British Mushrooms & Toadstools. HarperCollins. p. 192. ISBN 978-0-00-723224-6.
  9. Phillips, Roger (1981). Mushrooms and Other Fungi of Great Britain and Europe. London: Pan Books. p. 150. ISBN 0-330-26441-9.
  10. Pegler, David N. (1983). Mushrooms and Toadstools. London: Mitchell Beazley Publishing. p. 119. ISBN 0-85533-500-9.
  11. Tedersooa, Leho; Suvia, Triin; Larssonb, Ellen; Kõljalga, Zas (2006). "Diversity and community structure of ectomycorrhizal fungi in a wooded meadow". Mycological Research. 110 (6): 734–48. doi:10.1016/j.mycres.2006.04.007. PMID 16769208.
  12. Kibby, Geoffrey (2003). Mushrooms and Toadstools of Britain and Northern Europe. Hamlyn. p. 99. ISBN 978-0-7537-1865-0.
  13. Saber, M. (1999). "The species of Inocybe in Iran". Iranian Journal of Plant Pathology. 35 (1–4): 7–11.
  14. Hall, Ian Robert; Buchanan, Peter K.; Stephenson, Steven L.; Yun, Wang; Cole, Anthony L. J. (2003). Edible and Poisonous Mushrooms of the World. Timber Press. pp. 108–109. ISBN 978-0-88192-586-9.


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