Alcohol Inky Cap
Coprinopsis atramentaria (Bull.)
Alcohol Inky Cap: https://marylandbiodiversity.com/species/18297
Synonyms
Tippler's Bane 
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16 Records

GAALWAFRCLMOHOBABCHACEPGAACVCHSMKEQACNTADOWISOWO

Status

Common names reflect unpleasant digestive reaction when eating this species and consuming alcohol.

Description

Cap: white when young through gray/gray-brown to black in age (as it deliquesces); oval; striated; margin may be upturned in age. Gills: white, then gray, finally black; free; crowded. Stalk: white; silky (J. Solem, pers. comm.).

Where To Find

In grass or on wood at base of tree.

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Source: Wikipedia

This article is about a mushroom. For its namesake, see Common ink.

Coprinopsis atramentaria
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Fungi
Division: Basidiomycota
Class: Agaricomycetes
Order: Agaricales
Family: Psathyrellaceae
Genus: Coprinopsis
Species:
C. atramentaria
Binomial name
Coprinopsis atramentaria
(Bull.) Redhead, Vilgalys & Moncalvo (2001)
Synonyms

Coprinus atramentarius

Coprinopsis atramentaria
View the Mycomorphbox template that generates the following list
Gills on hymenium
Cap is ovate
Hymenium is free
Stipe is bare
Spore print is blackish-brown
Ecology is saprotrophic
Edibility is edible or poisonous

Coprinopsis atramentaria, commonly known as the common ink cap, tippler's bane, or inky cap, is an edible (although poisonous when combined with alcohol) mushroom found in Europe and North America. Previously known as Coprinus atramentarius, it is the second best known ink cap and previous member of the genus Coprinus after C. comatus. It is a widespread and common fungus found throughout the northern hemisphere. Clumps of mushrooms arise after rain from spring to autumn, commonly in urban and disturbed habitats such as vacant lots and lawns, as well as grassy areas. The grey-brown cap is initially bell-shaped before opening, after which it flattens and disintegrates. The flesh is thin and the taste mild. It can be eaten, but due to the presence of coprine within the mushroom, it is poisonous when consumed with alcohol, as it heightens the body's sensitivity to ethanol in a similar manner to the anti-alcoholism drug disulfiram.

Taxonomy

[edit]

The common ink cap was first described by French naturalist Pierre Bulliard in 1786 as Agaricus atramentarius before being placed in the large genus Coprinus in 1838 by Elias Magnus Fries. The specific epithet is derived from the Latin word atramentum "ink".[1]

The genus was formerly considered to be a large one with well over 100 species. However, molecular analysis of DNA sequences showed that most species belonged in the family Psathyrellaceae, distinct from the type species that belonged to the Agaricaceae. It was given its current binomial name in 2001 as a result, as this and other species were moved to the new genus Coprinopsis.[2]

The term "tippler's bane" is derived from its ability to create acute sensitivity to alcohol, similar to disulfiram (Antabuse).[3] Other common names include common ink cap and inky cap. The black liquid that this mushroom releases after being picked was once used as ink.[4]

Description

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A group of young common ink cap mushrooms

Measuring 3–10 cm (1+1⁄8–3+7⁄8 in) in diameter, the greyish or brownish-grey cap[5] is initially bell-shaped, is furrowed, and later splits. The colour is more brownish in the centre of the cap, which later flattens before melting. The very crowded gills are free; they are whitish at first but rapidly turn black and easily deliquesce. The short stipe measures 5–17 cm (2–6+3⁄4 in) high by 1–2 cm in diameter,[5] is grey in colour, and lacks a ring. In young groups, the stems may be obscured by the caps.[6] The spore print is black,[7][8] and the almond-shaped spores measure 8–11 by 5–6 μm.[9] The flesh is thin and pale grey in colour.[3]

Distribution and habitat

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Ink cap tuft. New Zealand, March 2021.
Ink cap spilling "ink". Ruler for scale. New Zealand, March 2021.

Coprinopsis atramentaria occurs across the Northern Hemisphere, including Europe, North America, and Asia,[10] but has also been found in Australia,[11] where it has been recorded from such urban locations as the Royal Botanic Gardens in Sydney and around Lake Torrens,[12] and also in South Africa.[13] Recent finds of ink caps (photographs inserted on the right) in Dunedin on New Zealand's South Island have been identified as C. atramentaria and Coprinellus micaceus, a related species which also releases a black ink once used for printing[14] (though the exact species is still to be confirmed).[better source needed] in the process known as deliquescence.

Like many ink caps, it grows in tufts. It is commonly associated with buried wood and is found in grassland, meadows, disturbed ground, and open terrain from late spring to autumn. Fruiting bodies have been known to push their way up through asphalt[11] and even tennis courts.[15] It is also common in urban areas and appears in vacant lots, and tufts of fungi can be quite large and fruit several times a year. If dug up, the mycelium can often be found originating on buried dead wood.[16]

Toxicity and uses

[edit]
Chemical structure of coprine
Black cap fungi, Rabindra Sarobar, Kolkata

Consuming Coprinopsis atramentaria within a few hours of alcohol results in a "disulfiram syndrome".[17][18] This interaction has only been known since the early part of the twentieth century. Symptoms include facial reddening, nausea, vomiting, malaise, agitation, palpitations, and tingling in limbs, and arise five to ten minutes after consumption of alcohol.[19] If no more alcohol is consumed, they will generally subside over two or three hours. Symptom severity is proportional to the amount of alcohol consumed, becoming evident when blood alcohol concentration reaches 5 mg/dl, and prominent at concentrations of 50–100 mg/dl. Disulfiram has, however, been known to cause myocardial infarction (heart attack).[20] The symptoms can occur if even a small amount of alcohol is consumed up to three days after eating the mushrooms, although they are milder as more time passes.[21] Rarely, a cardiac arrhythmia, such as atrial fibrillation on top of supraventricular tachycardia, may develop.[21] Because of these effects, in some cases, the mushroom has been used to cure alcoholism.[22]

The fungus contains a cyclopropylglutamine compound called coprine.[23] Its active metabolite, 1-aminocyclopropanol, blocks the action of an enzyme, acetaldehyde dehydrogenase, which breaks down acetaldehyde in the body.[24] Acetaldehyde is an intermediate metabolite of ethanol and is responsible for most symptoms of a hangover; its effect on autonomic β receptors is responsible for the vasomotor symptoms.[23]

Treatment involves reassuring the patient that the often frightening symptoms will pass, rehydration (fluid replacement) for fluid loss from vomiting, and monitoring for cardiac arrhythmias.[25]

Large and prolonged doses of coprine were found to have gonadotoxic effects on rats and dogs in testing.[26]

See also

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Notes

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  1. ^ Nilson S & Persson O (1977). Fungi of Northern Europe 1: Larger Fungi (Excluding Gill-Fungi). Penguin. p. 72. ISBN 0-14-063005-8.
  2. ^ Redhead, Scott A; Vilgalys, Rytas; Moncalvo, Jean-Marc; Johnson, Jacqui; Hopple Jr. John S (2001). "Coprinus Pers. and the disposition of Coprinus species sensu lato". Taxon. 50 (1). International Association for Plant Taxonomy (IAPT): 203–41. doi:10.2307/1224525. JSTOR 1224525.
  3. ^ a b Arora, David (1986). Mushrooms demystified: a comprehensive guide to the fleshy fungi (2nd ed.). Berkeley: Ten Speed Press. pp. 347–48. ISBN 0-89815-169-4.
  4. ^ Hall, Ian; et al. (August 1, 2003). Edible and Poisonous Mushrooms of the World. Timber Press. Portland, Oregon. ISBN 978-0-88192-586-9. p. 198.
  5. ^ a b Davis, R. Michael; Sommer, Robert; Menge, John A. (2012). Field Guide to Mushrooms of Western North America. Berkeley: University of California Press. p. 206. ISBN 978-0-520-95360-4. OCLC 797915861.
  6. ^ Trudell, Steve; Ammirati, Joe (2009). Mushrooms of the Pacific Northwest. Timber Press Field Guides. Portland, OR: Timber Press. pp. 196–197. ISBN 978-0-88192-935-5.
  7. ^ Pouliot, Alison; May, Tom (March 2021). Wild Mushrooming: A Guide for Foragers. Csiro Publishing. p. 116. ISBN 978-1-4863-1174-3.
  8. ^ Baroni, Timothy J. (2017-07-12). Mushrooms of the Northeastern United States and Eastern Canada. Timber Press. p. 330. ISBN 978-1-60469-634-9.
  9. ^ Phillips, Roger (2006). Mushrooms. Pan MacMillan. p. 258. ISBN 0-330-44237-6.
  10. ^ Uljé, Kees. "Coprinus atramentarius (Bull.: Fr.) Fr. - Epicrisis: 243. 1838". Coprinus (studies in coprinus). Retrieved 2009-07-31.
  11. ^ a b Fuhrer B (2005). A Field Guide to Australian Fungi. Melbourne: Bloomings Books. p. 43. ISBN 1-876473-51-7.
  12. ^ Cleland JB (1976). Toadstools and mushrooms and other larger fungi of South Australia. South Australian Government Printer. p. 159.
  13. ^ Reid, Derek A.; Eicker, Albert (1999). "South African fungi 10: New species, new records and some new observations". Mycotaxon. 73: 169–97.
  14. ^ Hall, Ian; et al. (August 1, 2003). Edible and Poisonous Mushrooms of the World. Timber Press. Portland, Oregon. ISBN 978-0-88192-586-9. p. 198
  15. ^ Ramsbottom 1953, p. 128.
  16. ^ Ramsbottom 1953, p. 196.
  17. ^ Benjamin 1995, p. 284.
  18. ^ Michelot, Didier (1992). "Poisoning by Coprinus atramentarius". Natural Toxins. 1 (2): 73–80. doi:10.1002/nt.2620010203. PMID 1344910.
  19. ^ Benjamin 1995, p. 288.
  20. ^ Disulfiramlike Mushroom Toxicity at eMedicine
  21. ^ a b Benjamin 1995, p. 289.
  22. ^ Phillips, Roger (2010). Mushrooms and Other Fungi of North America. Buffalo, NY: Firefly Books. p. 235. ISBN 978-1-55407-651-2.
  23. ^ a b Benjamin 1995, p. 286.
  24. ^ Marchner, H.; Tottmar, O. (1978). "A Comparative Study on the Effects of Disulfiram, Cyanamide and 1-Aminocyclopropanol on the Acetaldehyde Metabolism in Rats". Acta Pharmacologica et Toxicologica. 43 (3): 219–32. doi:10.1111/j.1600-0773.1978.tb02258.x. PMID 707135.
  25. ^ Benjamin 1995, p. 290.
  26. ^ Jönsson, Monica; Lindquist, Nils Gunnar; Plöen, Leif; Ekvärn, Sven; Kronevi, Tony (1979). "Testicular lesions of coprine and benzcoprine". Toxicology. 12 (2): 89–100. doi:10.1016/0300-483X(79)90035-0. PMID 473235.

References

[edit]
  • Benjamin, Denis R. (1995). Mushrooms: poisons and panaceas—a handbook for naturalists, mycologists and physicians. New York: WH Freeman and Company. ISBN 0-7167-2600-9.
  • Ramsbottom, J (1953). Mushrooms & Toadstools. Collins. ISBN 1-870630-09-2.

Further reading

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Wikimedia Commons has media related to Coprinopsis atramentaria.
  • North, Pamela (1967). Poisonous Plants and Fungi in colour. Blandford Press & Pharmacological Society of Great Britain.