(Bull. ex Fr.) P. Karst.
|pores on hymenium|
|no distinct cap|
|hymenium is decurrent|
|lacks a stipe|
|spore print is white|
|ecology is parasitic|
Piptoporus betulinus, commonly known as the birch polypore, birch bracket, or razor strop, is one of the most common polyporous bracket fungi and, as the name suggests, grows almost exclusively on birch trees. The brackets burst out from the bark of the tree, and these fruiting bodies can last for more than a year. Technically, it is an edible mushroom, with a strong, pleasant "mushroomy" odor but a bitter taste. The velvety cut surface of the fruiting body was traditionally used as a strop for finishing the finest of edges on razors. It is also said to have medicinal properties, and this fungus was carried by "Ötzi the Iceman" – the 5,000-year-old mummy found in Tyrol.
The fruiting bodies (basidiocarps) are pale, with a smooth greyish-brown top surface, with the underside a creamy white and with hundreds of pores that contain the spores. The fruiting body has a rubbery texture, becoming corky with age. Wood decayed by the fungus, and cultures of its mycelium, often smell distinctly of green apples. The spores are cylindrical to ellipsoid in shape, and measure 3–6 by 1.5–2 μm.
P. betulinus has a bipolar mating system where monokaryons or germinating spores can only mate and form a fertile dikaryon with an individual that possesses a different mating-type factor. There are at least 33 different mating-type factors within the British population of this fungus. These factors are all variants or alleles of a single gene, as opposed to the tetrapolar mating system of some other basidiomycete species, which involves two genes.
Range and ecology
The geographic distribution of Piptoporus betulinus appears to be restricted to the Northern Hemisphere. There is some doubt about the ability of isolates from the European continent, North America and the British Isles to interbreed.
It is a necrotrophic parasite on weakened birches, and will cause brown rot and eventually death, being one of the most common fungi visible on dead birches. It is likely that the birch bracket fungus becomes established in small wounds and broken branches and may lie dormant for years, compartmentalised into a small area by the tree's own defence mechanisms, until something occurs to weaken the tree. Fire, drought and suppression by other trees are common causes of such stress.
In most infections there is only one fungal individual present, but occasionally several individuals may be isolated from a single tree, and in these cases it is possible that the birch bracket fungus entered after something else killed the tree. These fungal "individuals" can sometimes be seen if a slice of brown-rotted birch wood is incubated in a plastic bag for several days. This allows the white mycelium of the fungus to grow out of the surface of the wood. If more than one individual dikaryon is present, lines of intraspecific antagonism form as the two individual mycelia interact and repel each other.
The fungus can harbor a large number of species of insects that depend on it for food and as breeding sites. In a large-scale study of over 2600 fruit bodies collected in eastern Canada, 257 species of arthropods, including 172 insects and 59 mites, were found. The fungus is eaten by the caterpillars of the fungus moth Nemaxera betulinella.
Piptoporus betulinus 01.jpg
- Forest pathology
- Medicinal mushrooms
- Fomes fomentarius also carried by Ötzi the Iceman
- Ganoderma applanatum known as the Artist's conk
- Capasso L (December 1998), "5300 years ago, the Ice Man used natural laxatives and antibiotics", Lancet, 352 (9143): 1864, PMID 9851424, doi:10.1016/S0140-6736(05)79939-6
- Volk, Tom. "Public Description of Piptoporus betulinus (Bull.) P. Karst.". Mushroom Observer. Retrieved 9 June 2011.
- Adams, T J H (1982). Piptoporus betulinus: Some aspects of population biology. (PhD thesis): Exeter University.
- Michael Kuo; Andy Methven (2010). 100 Cool Mushrooms. University of Michigan Press. p. 141. ISBN 978-0-472-03417-8.
- MycoBank. "Piptoporus betulinus". Fungal databases. International Mycological Association. Retrieved 11 June 2011.
- Cant, D (1980). Population studies on Piptoporus betulinus with special reference to the mating system. (PhD thesis): Lancaster University.
- Burnett, J H (1975). Mycogenetics: Introduction to the General Genetics of Fungi. Wiley. p. 390. ISBN 978-0-471-12445-0.
- Adams, T J H; NK Todd; ADM Rayner (1981). "Antagonism between dikaryons of Piptoporus betulinus.". Transactions of the British Mycological Society. 76 (3): 510–513. doi:10.1016/s0007-1536(81)80085-x.
- Quentin Wheeler; Meredith Blackwell (1984). Fungus-Insect Relationships: Perspectives in Ecology and Evolution. Columbia University Press. p. 147. ISBN 978-0-231-05695-3.
- Wangun HV, Berg A, Hertel W, Nkengfack AE, Hertweck C. (Nov 2004), "Anti-inflammatory and anti-hyaluronate lyase activities of lanostanoids from Piptoporus betulinus.", J Antibiot (Tokyo), Germany, 57 (11): 755–8, PMID 15712671, doi:10.7164/antibiotics.57.755
- Kamo T, Asanoma M, Shibata H, Hirota M. (Aug 2003), "Anti-inflammatory lanostane-type triterpene acids from Piptoporus betulinus.", J Nat Prod., 66 (8): 1104–6, PMID 12932134, doi:10.1021/np0300479
- Schlegel B, Luhmann U, Härtl A, Gräfe U. (Sep 2000), "Piptamine, a new antibiotic produced by Piptoporus betulinus Lu 9-1.", J Antibiot (Tokyo), 53 (9): 973–4, PMID 11099232, doi:10.7164/antibiotics.53.973
- Simon Singh; Edzard Ernst (2009). Trick Or Treatment: The Undeniable Facts About Alternative Medicine. W. W. Norton. pp. 193–. ISBN 978-0-393-33778-5.
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