Amanita bisporigera
Amanita bisporigera | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Fungi |
Division: | Basidiomycota |
Class: | Agaricomycetes |
Order: | Agaricales |
Family: | Amanitaceae |
Genus: | Amanita |
Species: | A. bisporigera
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Binomial name | |
Amanita bisporigera G.F.Atk. (1906)
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Synonyms[1][2] | |
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Amanita bisporigera | |
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Gills on hymenium | |
Cap is convex or flat | |
mycorrhizal | |
Edibility is deadly |
Amanita bisporigera is a deadly
A. bisporigera was
Description
The cap is 3–10 centimetres (1–4 inches) in diameter and, depending on its age, ranges in shape from egg-shaped to convex to somewhat flattened. The cap surface is smooth and white, sometimes with a pale tan- or cream-colored tint in the center. The surface is either dry or, when the environment is moist, slightly sticky. The flesh is thin and white, and does not change color when bruised.[4] The margin of the cap, which is rolled inwards in young specimens, does not have striations (grooves), and lacks volval remnants. The gills, also white, are crowded closely together. They are either free from attachment to the stipe or just barely reach it. The lamellulae (short gills that do not extend all the way to the stipe) are numerous, and gradually narrow.
The white stipe is 6–14 cm (2+1⁄2–5+1⁄2 in) by 0.7–1.8 cm (1⁄4–3⁄4 in) thick, solid (i.e., not hollow), and tapers slightly upward. The surface, in young specimens especially, is frequently floccose (covered with tufts of soft hair), fibrillose (covered with small slender fibers), or squamulose (covered with small scales); there may be fine grooves along its length. The bulb at the base of the stipe is spherical or nearly so. The delicate ring on the upper part of the stipe is a remnant of the partial veil that extends from the cap margin to the stalk and covers the gills during development. It is white, thin, membranous, and hangs like a skirt. When young, the mushrooms are enveloped in a membrane called the universal veil, which stretches from the top of the cap to the bottom of the stipe, imparting an oval, egg-like appearance. In mature fruit bodies, the veil's remnants form a membrane around the base, the volva, like an eggshell-shaped cup. On occasion, however, the volva remains underground or gets torn up during development. It is white, sometimes lobed, and may become pressed closely to the stipe.[5] The volva is up to 3.8 cm (1+1⁄2 in) in height (measured from the base of the bulb), and is about 2 mm thick midway between the top and the base attachment.[6] The mushroom's odor has been described as "pleasant to somewhat nauseous",[4] becoming more cloying as the fruit body ages.[6] The cap flesh turns yellow when a solution of potassium hydroxide (KOH, 5–10%) is applied (a common chemical test used in mushroom identification). This characteristic chemical reaction is shared with A. ocreata and A. virosa, although some authors have expressed doubt about the identity of North American A. virosa, suggesting those collections may represent four-spored A. bisporigera.[6][7] Tulloss suggests that reports of A. bisporigera that do not turn yellow with KOH were actually based on white forms of A. phalloides.[6] Findings from the Chiricahua Mountains of Arizona and in central Mexico, although "nearly identical" to A. bisporigera, do not stain yellow with KOH; their taxonomic status has not been investigated in detail.[2]
Microscopic features
In 1906 Charles E. Lewis studied and illustrated the development of the basidia in order to compare the nuclear behavior of the two-spored with that of the four-spored forms. Initially (1), the young basidium, appearing as a club-shaped branch from the subhymenium, is filled with cytoplasm and contains two primary nuclei, which have distinct nucleoli. As the basidium grows larger, the membranes of the two nuclei contact (2), and then the membrane disappears at the point of contact (3). The two primary nuclei remain distinct for a short time, but eventually the two nuclei fuse completely to form a larger secondary nucleus with a single secondary nucleolus (4, 5). The basidium increases in size after the primary nuclei fuse, and the nucleus migrates towards the end of the basidia (6, 7). During this time, the nucleus develops vacuoles "filled by the nuclear sap in the living cell". Chromosomes are produced from the nucleolar threads, and align transversely near the apex of the basidium, connected by spindles (8–10). The chromosomes then move to the poles, forming the daughter nuclei that occupy different positions in the basidium; the daughters now have a structure similar to that of the parent nuclei (11). The two nuclei then divide to form four nuclei, similar to fungi with four-spored basidia (12, 13). The four nuclei crowd together at some distance from the end of the basidium to form an irregular mass (14). Shortly thereafter, the sterigmata (slender projections of the basidia that attach the spores) begin to form (15), and cytoplasm begins to pass through the sterigmata to form the spores (16). Although Lewis was not able to clearly determine from observation alone whether the contents of two or four nuclei passed through the sterigmata, he deduced, by examining older basidia with mature spores, that only two nuclei enter the spores (16, 17).[8]
Genome
The Amanita Genome Project was begun in Jonathan Walton's lab at
The genetic sequence information from A. bisporigera has been used to identify molecular
Similar species
The color and general appearance of A. bisporigera are similar to those of A. verna and A. virosa. A. bisporigera is at times smaller and more slender than either A. verna or A. virosa, but it varies considerably in size; therefore size is not a reliable diagnostic characteristic.[4] A. virosa fruits in autumn—later than A. bisporigera.[16] A. elliptosperma is less common but widely distributed in the southeastern United States, while A. ocreata is found on the West Coast and in the Southwest. Other similar toxic North American species include Amanita magnivelaris, which has a cream-colored, rather thick, felted-submembranous, skirt-like ring,[17] and A. virosiformis, which has elongated spores that are 3.9–4.7 by 11.7–13.4 μm.[18] Neither A. elliptosperma nor A. magnivelaris typically turn yellow with the application of KOH;[19][20] the KOH reaction of A. virosiformis has not been reported.[21]
Leucoagaricus leucothites is another all-white mushroom with an annulus, free gills, and white spore print, but it lacks a volva and has thick-walled dextrinoid (staining red-brown in Melzer's reagent) egg-shaped spores with a pore.[22][23] A. bisporigera may also be confused with the larger edible species Agaricus silvicola, the "horse-mushroom". Like many white amanitas, young fruit bodies of A. bisporigera, still enveloped in the universal veil, can be confused with puffball species, but a longitudinal cut of the fruit body reveals internal structures in the Amanita that are absent in puffballs.[24] In 2006, seven members of the Hmong community living in Minnesota were poisoned with A. bisporigera because they had confused it with edible paddy straw mushrooms (Volvariella volvacea) that grow in Southeast Asia.[25]
Taxonomy
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Relationships of Amanita bisporigera and related species based on ITS sequence data. The A. virosa specimen was collected from Japan, A. bisporigera from the US, and the other species from China.[26] |
Amanita bisporigera was first described scientifically in 1906 by American botanist
Amanita bisporigera belongs to
Distribution and habitat
Like most other Amanita species, A. bisporigera is thought to form
Toxicity
A. bisporigera is considered the most toxic North American Amanita mushroom, with little variation in toxin content between different fruit bodies.
The first reported poisonings resulting in death from the consumption of A. bisporigera were from near
See also
- List of Amanita species
- List of deadly fungi
- Silibinin – a liver-protecting compound used in cases of Amanita mushroom poisoning
References
- ^ "Amanitina bisporigera (G.F. Atk.) E.-J. Gilbert 1941". MycoBank. International Mycological Association. Retrieved 2010-05-27.
- ^ a b c d Tulloss R, Pussiel L (2005-07-16). "Key to Species of AMANITA Section PHALLOIDEAE from North and Central America". Amanita studies. Retrieved 2010-05-28.
- ^ "Standardized Common Names for Wild Species in Canada". National General Status Working Group. 2020.
- ^ ISBN 978-0-88902-977-4.
- ^ a b c d Jenkins, 1986, pp. 140–41.
- ^ a b c d e f g Tulloss R. "Amanita bisporigera G. F. Atk". Amanita studies. Archived from the original on 2011-05-15. Retrieved 2010-05-27.
- ^ a b Kuo M. (October 2003). "Amanita bisporigera". MushroomExpert.Com. Archived from the original on 5 May 2010. Retrieved 2010-05-26.
- ^ JSTOR 2465725.
- ^ Hallen HE, Walton J. "The Amanita Genome Project: Scientific Importance". Michigan State University. Archived from the original on 2011-06-07. Retrieved 2010-05-27.
- PMID 27978833.
- ^ "BLAST Search". Amanita bisporigera Genome Project BLAST Page. Michigan State University DOE Plant Research Laboratory and the Bioinformatics Core of the Research Technology Support Facility at MSU. Archived from the original on 2006-09-01. Retrieved 2010-07-10.
- ^ PMID 18025465.
- S2CID 10017676.
- doi:10.1111/j.1471-8286.2005.01198.x. Archived from the originalon 2006-09-19.
- S2CID 969884.
- ^ ISBN 978-0-472-85610-7.
- ^ Tulloss R. (2009). "Amanita magnivelaris Peck". Amanita studies. Archived from the original on 2011-07-16. Retrieved 2010-05-28.
- ^ Jenkins, 1986, p. 146.
- ^ Tullos R. "Amanita elliptosperma G.F. Atk., A. gwyniana Coker, A. hygroscopica Coker, A. parviformis (Murrill) Murrill, A. pseudoverna (Murrill) Murrill, A. verniformis (Murrill) Murrill". Amanita Studies. Archived from the original on 2011-07-14. Retrieved 2010-06-28.
- ^ Tulloss R. "Amanita magnivelaris Peck". Amanita Studies. Archived from the original on 2011-07-14. Retrieved 2010-06-28.
- ^ Jenkins, 1986, p. 141.
- ISBN 978-0-8493-0194-0.
- ISBN 978-0-7627-3109-1.
- ISBN 978-0-88192-935-5.
- PMID 17966265.
- ^ PMID 16198510.
- ^ Gilbert E-J (1940). "Amanitaceae". Iconographia Mycologica. 27 (Suppl. 1): 78.
- ISBN 978-0-85199-826-8.
- ^ Murrill WA (1944). "More fungi from Florida". Lloydia. 7 (4): 303–327.
- ^ Jenkins DT (1979). "A study of Amanita types III. Taxa described by W. A. Murrill". Mycotaxon. 10 (1): 175–200. Archived from the original on 2015-09-23. Retrieved 2010-05-28.
- ^ Peck CH (1902). "Report of the State Botanist 1901". Bulletin of the New York State Museum. 54: 931–982.
- .
- JSTOR 3761246.
- ^ Jenkins, 1986, p. 5.
- PMID 4773309.
- PMID 5951044.
- ISBN 978-0-7817-2845-4.
- ^ S2CID 30160371.
- ISBN 978-0-7167-2649-4.
- ISBN 978-0-88192-586-9.
- S2CID 29289507.
- ISBN 978-0-8247-8652-6.
- ^ Helm R. (1957). "Sur un cas d'empoisonnement mortel cause au Mexique par l'Amanita bisporigera Atk" [On a case of fatal poisoning caused by Amanita bisporigera Atk. in Mexico]. Revue de Mycologie (in French). 22 (2): 208–216.
- PMID 8656182.
Cited books
- Jenkins DB (1986). Amanita of North America. Eureka, California: Mad River Press. ISBN 978-0-916422-55-4.
External links
- Media related to Amanita bisporigera at Wikimedia Commons