Geopyxis carbonaria
Geopyxis carbonaria | |
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Scientific classification | |
Kingdom: | Fungi |
Division: | Ascomycota |
Class: | Pezizomycetes |
Order: | Pezizales |
Family: | Pyronemataceae |
Genus: | Geopyxis |
Species: | G. carbonaria |
Binomial name | |
Geopyxis carbonaria (Alb. & Schwein.) Sacc. (1889) | |
Synonyms[1] | |
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Geopyxis carbonaria is a species of fungus in the genus Geopyxis, family Pyronemataceae. First described to science in 1805, and given its current name in 1889, the species is commonly known as the charcoal loving elf-cup, dwarf acorn cup, stalked bonfire cup, or pixie cup. The small, goblet-shaped fruitbodies of the fungus are reddish-brown with a whitish fringe and measure up to 2 cm (0.8 in) across. They have a short, tapered stalk. Fruitbodies are commonly found on soil where brush has recently been burned, sometimes in great numbers. The fungus is distributed throughout many temperate regions of the Northern Hemisphere. It is found in Europe, Turkey, and North America. Although it is primarily a saprotrophic species, feeding on the decomposing organic matter remaining after a fire, it also forms biotrophic associations with the roots of Norway spruce.
Taxonomy
The fungus was first described scientifically in 1805 by Johannes Baptista von Albertini and Lewis David de Schweinitz as Peziza carbonaria.[2] Mordecai Cubitt Cooke illustrated the fruitbodies, spores, and asci in his 1879 work Mycographia, seu Icones fungorum. Figures of fungi from all parts of the world.[3] In 1889, Pier Andrea Saccardo transferred the fungus to the genus Geopyxis, giving the species its current name.[4] Pustularia carbonaria, published by Heinrich Rehm in 1884,[5] is a synonym of G. carbonaria.[1] Louis-Joseph Grélet proposed the variety Geopyxis carbonaria var. sessilis in 1937, referring to forms producing fruitbodies without a stalk, but the taxon is not considered to have independent taxonomic significance.[6] In 1860 Miles Berkeley and Moses Ashley Curtis described the species Peziza lepida from collections made in Japan as part of the North Pacific Exploring and Surveying Expedition (1853–1856).[7] This taxon was synonymized with G. carbonaria by Mien Rifai in 1968, a taxonomic opinion corroborated by Donald Pfister about a decade later.[8]
The specific epithet carbonaria derives from the Latin word for "charcoal".[9] Common names given to the fungus include "charcoal loving elf-cup", "dwarf acorn cup",[10] "pixie cup",[11] and the British Mycological Society approved "stalked bonfire cup".[12]
Description
The fruitbodies (ascocarps) of Geopyxis carbonaris are cup shaped, 1–2 cm wide, and have fringed whitish margins. The inner spore-bearing surface of the cup, the hymenium, is brick red and smooth, while the exterior surface is a dull yellow, and may be either smooth or have blister-like spots (pustules). The stipe is small (1–1.5 mm long and 1–2 mm wide), whitish in color, and expands abruptly into the cup.[13] The brownish flesh of the fungus is thin and brittle. It does not have any distinctive taste, but has an unpleasant smell when crushed in water.[14] The edibility of the fungus is not known, but the fruitbodies are insubstantial and unlikely to be harvested for eating.[11]
Microscopic characteristics
In mass, the spores are whitish.[9] The spores are elliptical, smooth, hyaline, devoid of oil droplets (eguttulate), and have dimensions of 13–18 by 7–9 µm.[15] They are thin walled and germinate and grow rapidly in vitro in the absence of external stimuli.[16] The asci are 190–225 by 9–10 µm. The paraphyses are slightly club-shaped, unbranched, and have irregular orange-brown granules, with tips up to 5 µm wide, and are not forked or lobed. The hypothecium, the layer of cells below the hymenium, is made of densely packed, small irregular cells.[15]
Similar species
The closely related vulcan elf cup (Geopyxis vulcanalis) has a pale orange to yellowish fruitbody that is deeply cup shaped before flattening in maturity, and its crushed flesh often has an odor of sulfur. It may be distinguished microscopically by its paraphyses, which lack the orange-brown granules characteristic of G. carbonaria. It also has larger spores, measuring 14–22 by 8–11 µm. Unlike G. carbonaria, it grows on substrates other than burned wood, including mosses, and needle duff.[17] Tarzetta cupularis, which grows habitats similar to G. carbonaria, is distinguished microscopically by its spores that contain two oil droplets. Other genera with similar species with which G. carbonaria may be confused in the field include Aleuria, Caloscypha, Melastiza, and Sowerbyella.[18]
Habitat and distribution
Geopyxis carbonaria is widespread on burned soil or charcoal in the spring and throughout the growing season.[15] It is one of the most common pioneer species found on burned ground.[9] The charred litter on the forest floor increases the underlying soil pH as well as the availability of minerals.[19] Fruitbodies are produced from 16 to 139 weeks after a forest fire in areas with coniferous trees.[20] Most fruitbodies are produced in the first year after a burn. The fungus prefers fruiting in microhabitats with thin postfire duff near standing burned tree trunks. Geopyxis carbonaria fruitbodies are often found in the same post-fire stands as morels, although the former is usually more abundant.[21] Because the pixie cup fruits earlier than morels, it may serve as an indicator of imminent morel fruiting.[22] Other cup fungi often found fruiting in the same area as G. carbonaria include those from the genera Aleuria, Anthracobia, Peziza, and Tarzetta.[23]
The fungus is found in Europe (from where it was originally described),[24] and is widespread throughout North America. The North American distribution extends north to Alaska.[11] In 2010, it was reported for the first time from Turkey.[14]
Ecology
Although primarily a saprotrophic fungus involved in the post-fire breakdown of duff and coniferous roots, Geopyxis carbonaria has been shown to be capable of forming ectomycorrhizae with Norway spruce (Picea abies).[16] It had been demonstrated earlier in laboratory experiments that the fungus has a biotrophic interaction with lodgepole pine (Pinus contorta). The hyphae of G. carbonaria were able to infect the cortex of the tree seedling, but did not penetrate the endodermis. These traits suggest that the fungus is a moderate pathogen, with limited ability to cause reductions in seed germination.[25][26] Additionally, the fungus produces the enzyme polyphenol oxidase, and can break down the complex organic polymer lignin—features characteristic of saprotrophic fungi.[27] The formation of a rudimentary Hartig net, a characteristic of mycorrhizal fungi, indicated that G. carbonaria might be capable of forming mutualistic relationships under the right conditions. Vrålstad and colleagues suggest that its below-ground association with spruce roots protects it from physical damage in the event of a fire, and the extensive fruitbody production after a fire may reflect "a successful fungal escape from a dying host where the fungus no longer can maintain its biotrophic association".[16]
Large fruitings of the fungus are often associated with damage to the host tree, such as that which occurs with burning. A field study conducted in Norway demonstrated that fruit bodies were more likely to be found in areas that were heavily burned, compared to locations with light to moderate burning where the trees remained viable, or in clearcut areas. Fruiting was much denser in spruce forests—with up to 700–1000 fruitbodies per square meter—than in pine forests, where fruitbodies were sporadic.[16] Fruitbodies grew by the millions in the year following the Yellowstone fires of 1988.[9]
References
- 1 2 "GSD Species Synonymy: Geopyxis carbonaria (Alb. & Schwein.) Sacc.". Species Fungorum. CAB International. Retrieved 2015-07-07.
- ↑ Albertini JB, von Schweinitz LD. (1805). Conspectus Fungorum in Lusatiae superioris (in Latin). Leipzig, Germany. p. 314.
- ↑ Cooke MC. (1879). Mycographia, seu Icones fungorum. Figures of fungi from all parts of the world, drawn and illustrated by M. C. Cooke. Volume 1. Discomycetes, part 1. London, UK: Williams & Norgate. p. plate 74 (figure 284).
- ↑ Saccardo PA. (1889). Discomyceteae et Phymatosphaeriaceae. Sylloge Fungorum (in Latin) 8. p. 71.
- ↑ Rehm H. (1884). "Ascomyceten fasc. XV(1)". Hedwigia (in German) 23 (4): 49–57.
- ↑ "Geopyxis carbonaria var. sessilis Grélet". Index Fungorum. CAB International. Retrieved 2015-07-07.
- ↑ Berkeley J, Curtis MA. (1860). "Characters of new fungi collected in the North Pacific Exploring Expedition by Charles Wright". Proceedings of the American Academy of Arts and Sciences 4: 111–130 (see p. 127).
- ↑ Pfister DH. (1979). "Type studies in the genus Peziza: species described by Berkeley and Curtis from the United States North Pacific Exploring Expedition (1853–1856)". Mycotaxon 6 (2): 337–340.
- 1 2 3 4 Evenson VS. (1997). Mushrooms of Colorado and the Southern Rocky Mountains. Denver, USA: Westcliffe Publishers. p. 49. ISBN 978-1-56579-192-3.
- ↑ McKnight VB, McKnight KH. (1987). A Field Guide to Mushrooms: North America. Peterson Field Guides. Boston, Massachusetts: Houghton Mifflin. p. 60. ISBN 978-0-395-91090-0.
- 1 2 3 Laursen GA, Seppelt RD. (2009). Common Interior Alaska Cryptogams: Fungi, Lichenicolous Fungi, Lichenized Fungi, Slime Molds, Mosses, and Liverworts. College, Alaska: University of Alaska Press. p. 104. ISBN 978-1-60223-058-3.
- ↑ Holden EM. (2003). "Recommended English Names for Fungi in the UK" (PDF). British Mycological Society.
- ↑ Kupfer EM. (1902). "Studies on Urnula and Geopyxis". Bulletin of the Torrey Botanical Club 29 (3): 137–144. doi:10.2307/2478861.
- 1 2 Uzun Y, Demirel K, Kaya A, Gücin F. (2010). "Two new genus records for Turkish mycota". Mycotaxon 111: 477–480. doi:10.5248/111.477.
- 1 2 3 Tylutki EE. (1979). Mushrooms of Idaho and the Pacific Northwest. Moscow, Idaho: University Press of Idaho. p. 96. ISBN 978-0-89301-062-1.
- 1 2 3 4 Vrålstad T, Holst-Jensen A, Schumacher T. (1998). "The postfire discomycete Geopyxis carbonaria (Ascomycota) is a biotrophic root associate with Norway spruce (Picea abies) in nature". Molecular Ecology 7 (5): 609–616. doi:10.1046/j.1365-294x.1998.00365.x. PMID 9633103.
- ↑ Beug MW, Bessette AE, Bessette AR. (2014). Ascomycete Fungi of North America: A Mushroom Reference Guide. Austin, Texas: University of Texas Press. p. 143. ISBN 978-0-292-75452-2.
- ↑ Kimbrough JW, Gibson JL. (1990). "Ultrastructural and cytological observations of apothecial tissues of Geopyxis carbonaria (Pezizales, Ascomyetes)". Canadian Journal of Botany 68 (2): 243–257. doi:10.1139/b90-034.
- ↑ Adl SM. (2003). The Ecology of Soil Decomposition. Wallingford, UK: CAB International. p. 231. ISBN 978-0-85199-837-4.
- ↑ Petersen PM. (1970). "Danish fireplace fungi—an ecological investigation of fungi on burns". Dansk Botanisk Arkiv 27 (3): 6–97.
- ↑ Greene DF, Hesketh M, Pounden E. (2009). "Emergence of morel (Morchella) and pixie cup (Geopyxis carbonaria) ascocarps in response to the intensity of forest floor combustion during a wildfire". Mycologia 102 (4): 766–773. doi:10.3852/08-096. PMID 20648745.
- ↑ Obst J, Brown W, Artic Ecology and Development Consulting and Deton’cho Corporation (2000). Feasibility of a morel mushroom harvest in the Northwest Territories (Report). Yellowknife, Canada: Government of the Northwest Territories.
- ↑ Lincoff GH. (1989). National Audubon Society Field Guide to North American Mushrooms. New York, New York: AA Knopf. p. 351. ISBN 978-0-394-51992-0.
- ↑ Seaver FJ. (1928). The North American Cup-Fungi (Operculates). New York, New York: Hafner Publishing. p. 212.
- ↑ Egger KN, Paden JW. (1986). "Pathogenicity of postfire ascomycetes (Pezizales) on seeds and germinants of lodgepole pine". Canadian Journal of Botany 64 (10): 2368–2371. doi:10.1139/b86-312.
- ↑ Egger KN, Paden JW. (1986). "Biotrophic associations between lodgepole pine seedlings and postfire ascomycetes (Pezizales) in monoxenic culture". Canadian Journal of Botany 64 (11): 2719–2725. doi:10.1139/b86-359.
- ↑ Egger KN. (1986). "Substrate hydrolysis patterns of post-fire ascomycetes". Mycologia 87 (5): 771–780. doi:10.2307/3807522.
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