Superregnum: Eukaryota
Regnum: Fungi
Subregnum: Dikarya
Divisio: Basidiomycota
Subdivisio: Agaricomycotina
Classis: Agaricomycetes
Ordo: Polyporales
Familiae: Cerrenaceae – Dacryobolaceae – Fibroporiaceae – Fomitopsidaceae – Fragiliporiaceae – Ganodermataceae – Gelatoporiaceae – Grifolaceae – Hyphodermataceae – Incrustoporiaceae – Irpicaceae – Ischnodermataceae – Laetiporaceae – Meripilaceae – Meruliaceae – Panaceae – Phanerochaetaceae – Podoscyphaceae – Polyporaceae – Sparassidaceae – Steccherinaceae
Genera (incertae sedis): Aegeritopsis – Amaropostia – Amaurohydnum – Amauromyces – Amethicium – Amyloporia – Aquascypha – Auriporia – Australicium – Australohydnum – Austrolentinus – Bourdotiella – Bulbillomyces – Calcipostia – Candelabrochaete – Climacocystis – Columnodontia – Conohypha – Coralloderma – Cordochaete – Cryptomphalina – Cyanodontia – Cyanosporus – Cystidiopostia – Dendrophlebia – Diacanthodes – Diplomitoporus – Erastia – Faerberia – Fibroporia – Fuscopostia – Gilbertsonia – Globosomyces – Globuliciopsis – Gyrophanopsis – Henningsia – Hymenogramme – Hyphodontiastra – Hypochnicium – Inflatostereum – Irpicochaete – Laetifomes – Macrohyporia – Meruliophana – Mycoleptodonoides – Mycorrhaphoides – Nigrohydnum – Phanerodontia – Phaneroites – Phlebiella – Piptoporellus – Pseudofibroporia – Repetobasidiopsis – Rhodonia – Rickiopora – Roseofavolus – Roseograndinia – Ryvardenia – Sarcoporia – Skeletohydnum – Sparassiella – Spathulina – Spongioides – Spongipellis – Stegiacantha – Taiwanofungus – Uncobasidium
Name
Polyporales Gäum., Vergl. Morph. Pilze (Jena): 503 (1926)
References
Primary references
Gäumann, E. 1926. Vergleichende Morphologie der Pilze 1–626 [see page 503].
Links
Index Fungorum: IF 90565
MycoBank: MB 90565
Vernacular names
català: Poliporal
čeština: Chorošotvaré
Deutsch: Stielporlingsartige
lietuvių: Kempiniečiai
polski: Żagwiowce
Runa Simi: Hutk'ucha k'allampa
русский: Полипоровые
українська: Поліпоральні
中文: 多孔菌目
The Polyporales are an order of about 1800 species of fungi in the division Basidiomycota. The order includes some (but not all) polypores as well as many corticioid fungi and a few agarics (mainly in the genus Lentinus). Many species within the order are saprotrophic, most of them wood-rotters. Some genera, such as Ganoderma and Fomes, contain species that attack living tissues and then continue to degrade the wood of their dead hosts. Those of economic importance include several important pathogens of trees and a few species that cause damage by rotting structural timber. Some of the Polyporales are commercially cultivated and marketed for use as food items or in traditional Chinese medicine.
Taxonomy
History
The order was originally proposed in 1926 by Swiss mycologist Ernst Albert Gäumann to accommodate species within the phylum Basidiomycota producing basidiocarps (fruit bodies) showing a gymnocapous mode of development (forming the spore-bearing surface externally). As such, the order included the ten families Brachybasidiaceae, Corticiaceae, Clavariaceae, Cyphellaceae, Dictyolaceae, Fistulinaceae, Polyporaceae, Radulaceae, Tulasnellaceae, and Vuilleminiaceae, representing a mix of poroid, corticioid, cyphelloid, and clavarioid fungi.[5]
In a series of publications in 1932, E.J.H. Corner explained the occurrence of different types of hyphae in the fruit bodies of polypore fungi. He introduced the concept of hyphal analysis, which later become a fundamental character in polypore taxonomy.[6][7][8]
The order Polyporales was not widely adopted by Gäumann's contemporaries; most mycologists and reference works preferring to use the catch-all, artificial order Aphyllophorales for polypores and other "non-gilled fungi". When an attempt was made to introduce a more natural, morphology-based classification of the fungi in the 1980s and 1990s, the order was still overlooked. A standard 1995 reference work placed most polypores and corticioid fungi in the Ganodermatales, Poriales, and Stereales.[9]
Current status
/residual
/phlebioid
Phanerochaetaceae
Irpicaceae
Meruliaceae
Candelabrochaete africana
Steccherinaceae
Cerrenaceae*
Panaceae*
Hyphodermataceae
Meripilaceae
Podoscyphaceae
/hypochnicium & /climacocystis
/core polyporoid
Polyporaceae
Grifolaceae
/gelatoporia
Gelatoporiaceae*
Mycoleptodonoides vassiljevae
Auriporia aurea
/antrodia
Fomitopsidaceae
Laetiporaceae
/fibroporia + amyloporia
Dacryobolaceae
Sparassidaceae
/skeletocutis-tyromyces
Incrustoporiaceae
Ischnodermataceae
Simplified phylogenetic overview of the families (bolded) and clades (preceded with "/") recognized in Justo et al. 2017. Families marked with (*) were newly created.[10]
Molecular research, based on cladistic analysis of DNA sequences, has resurrected and redefined the Polyporales (also known as the polyporoid clade).[11][12][13] Studies using a combination of rRNA gene sequences, single-copy protein-coding genes, [14][15] and genome-based phylogenetic analyses have shown that the Polyporales are a monophyletic group.[13][16][10] They are a member of the class Agaricomycetes, but have not been assigned to a subclass.[17] Though the precise boundaries of the order and its constituent families are yet to be resolved, it retains the core group of polypores in the family Polyporaceae, with additional species in the Fomitopsidaceae and Meripilaceae. It also includes polypores in the Ganodermataceae, which were previously assigned to their own separate order, the Ganodermatales, based on their distinctive basidiospore morphology. Corticioid fungi belonging to the Cystostereaceae, Meruliaceae, Phanerochaetaceae, and Xenasmataceae are also included, as are the cauliflower fungi in the Sparassidaceae.[18]
In an extensive molecular analysis, Manfred Binder and colleagues analyzed 6 genes from 373 species and confirmed the existence of four previously recognized lineages of Polyporales: the antrodia, core polyporoid, phlebioid, and residual polyporoid clades.[13] Extending this work, Alfredo Justo and colleagues proposed a phylogenetic overview of the Polyporales that included a new family-level classification. They assigned family names to 18 clades and four informal unranked clades. The families are listed below, followed by their taxonomic authorities and year of publication:[10]
Phanerochaetaceae Jülich (1981)
Irpicaceae Spirin & Zmitr. (2003)
Meruliaceae Rea (1922)
Steccherinaceae Parmasto (1968)
Cerrenaceae Miettinen, Justo & Hibbett (2017)
Panaceae Miettinen, Justo & Hibbett (2017)
Hyphodermataceae Jülich (1981)
Meripilaceae Jülich (1981)
Podoscyphaceae D.A.Reid (1965)
Polyporaceae Corda (1939)
Fomitopsidaceae Jülich (1981)
Laetiporaceae Jülich (1981)
Dacryobolaceae Jülich (1981)
Sparassidaceae Jülich (1981)
Grifolaceae Jülich (1981)
Gelatoporiaceae Miettinen, Justo & Hibbett (2017)
Incrustoporiaceae Jülich (1981)
Ischnodermataceae Jülich (1981)
Other families that putatively belong to the Polyporales, but for which molecular confirmation is absent or lacking, include Diachanthodaceae Jülich, (1981); Fragiliporiaceae Y.C.Dai, B.K.Cui & C.L.Zhao (2015); Hymenogrammaceae Jülich (1981); and Phaeotrametaceae Popoff ex Piątek (2005).[10] The Nigrofomitaceae, formerly placed in the Polyporales, was shown to be nested as a distinct lineage within the Hymenochaetales.[19]
The family Steccherinaceae was redefined in 2012 to contain most species of the poroid and hydnoid genera Antrodiella, Junghuhnia, and Steccherinum, as well as members of 12 other hydnoid and poroid genera that had been traditionally classified in the families Phanerochaetaceae, Polyporaceae, and Meruliaceae.[15] Several new genera were added to the Steccherinaceae in 2016–17.[20][21]
Ecology
The order is cosmopolitan and contains around 1800 species of fungi worldwide—about 1.5% of all known fungus species.[10] All species in the Polyporales are saprotrophs, most of them wood-rotters. Their fruit bodies are therefore typically found on living or moribund trees or on dead attached or fallen wood. Polyporales species that fruit on the ground are either root rot species–such as Laetiporus cincinnatus and Grifola frondosa, or are fruiting from buried pieces of substrate–such as Polyporus radicatus and P. melanopus.[22]
Wood-decay Polyporales reduce the volume of dead wood in the forest and are an important component of the carbon cycle.[13] Wood is composed of primarily three types of tissue: lignin, cellulose, and hemicelluloses. White rot species of Polyporales are efficient degraders of the decay-resistant polymer lignin, leaving partially degraded cellulose as a residue.[13] Brown rot species break down the cellulose fibres, leaving a brittle, brown lignin residue. Brown-rot residues such as humus can remain in the soil for hundreds of years, increasing aeration and water-holding capacity.[23]
Peroxidase enzymes that degrade lignin, such as lignin peroxidase, manganese peroxidase, or versatile peroxidase, are present in all white-rot members of the Polyporales, but absent in brown-rot species.[16][24][25] Oxidase enzymes, including members of the glucose-methanol-choline oxidoreductase family, play a key role in the breakdown of plant polymers because they generate hydrogen peroxide, which acts as the ultimate oxidizer in both white-rot and brown-rot decay.[26]
Two species of Polyporales, Daedalea quercina and Fomitopsis pinicola, use paralysing toxins to destroy and colonize nematodes that feed on their fruit bodies.[27]
Importance
Sparassis crispa (left) and Laetiporus sulphureus are two edible Polyporales species
Many wood-decay fungi in the genera Fomes, Fomitopsis and Ganoderma are pathogenic, causing butt and root rot of living trees and consequent losses in forestry plantations. Several species, such as the mine fungus Fibroporia vaillantii, can rot and damage structural timber.[28]
Several of the Polyporales, notably Ganoderma lucidum (ling-zhi), Grifola frondosa (maitake),[29] Taiwanofungus camphoratus (niú zhāng zhī),[30] Lignosus rhinocerotis,[31] and Trametes versicolor (yun-zhi),[32] are commercially cultivated and marketed for use in traditional Chinese medicine. The polypores Laetiporus sulphureus, Fomes fomentarius, Fomitopsis pinicola, Fomitopsis betulina, and Laricifomes officinalis have been widely used in central European folk medicine for the treatment of various diseases.[33]
Some species, including several members of the genera Laetiporus and Sparassis, are used as food.[34] Blackfellow's bread, or Laccocephalum mylittae, is an edible that is prized by Aboriginal Australians.[35] Lentinus squarrosulus is collected and eaten in Asian and African communities.[36]
Fomitopsis betulina was formerly used in the manufacture of charcoal crayons.[37] Amadou, a spongy material derived from the fruit bodies of Fomes fomentarius, has been used since ancient times as a tinder. More recently, it has been used by dentists as a styptic, or as a felt-like material for making hats and other items.[38] The anise-scented fruit bodies of Haploporus odorus were used by some tribes of Plains Indians as a component of sacred objects. Laricifomes officinalis was used by nineteenth century Pacific northwest shamans for carving spirit figures.[39] Some species, including dyer's polypore (Phaeolus schweinitzii) and purple dye polypore (Hapalopilus nidulans) are used in mushroom dyeing.[40]
Sequenced genomes
Several member of the Polyporales have had their genomes sequenced to help understand the genetic basis for the production of enzymes involved in the synthesis of bioactive compounds, or to elucidate the metabolic pathways of wood decay, including Ganoderma lucidum,[41] Lignosus rhinocerotis,[42] Dichomitus squalens,[16] Fomitopsis pinicola,[16] Trametes versicolor,[16] and Wolfiporia cocos.[16] Two sequenced fungi, Phanerochaete chrysosporium,[43] and Postia placenta,[44] serve as model species for researchers investigating the mechanism of white rot and brown rot, respectively.[45][46] As of 2017, there have been 46 Polyporales genomes sequenced, representing about 7% of all sequenced fungal genomes.[10]
Fossil record
Fossilized fruit bodies of a Fomes species dating back to the Tertiary (66–2.6 Ma) were reported in Idaho in 1940.[47] A fossil fruit body of Ganodermites libycus was reported from the Early Miocene (23–2.6 Ma) in the Libyan Desert. This specimen is the earliest convincing fossil evidence for the Polyporales.[48]
Molecular clock techniques have been used to estimate the age of the Polyporales, suggesting that the order evolved either during the late Jurassic, about 203–250 Ma,[14] or, in more recent study, about 114 Ma.[49]
Genera Incertae sedis
There are several genera classified in the Polyporales that for various reason have not been assigned to a specific family. They are incertae sedis with respect to familial placement. Some may be poorly known and/or not included in DNA phylogenetic studies, or when they have been, did not clearly group with any named family (In some cases a new family must be created rather than the placement clarified.). These include:
Aegis Gómez-Montoya, Rajchenb. & Robledo (2017)[50]
Anthoporia Karasiński & Niemelä (2016)[51]
Bourdotiella Duhem & Schultheis (2011)[52]
Crustodontia Hjortstam & Ryvarden (2005)[53]
Crystallocystidium (Rick) Rick (1940)
Donkioporiella L.W.Zhou (2016)[54]
Globosomyces Jülich (1980)[55]
Globuliciopsis Hjortstam & Ryvarden (2004)[56]
Irpicochaete Rick (1940)[57]
Meruliophana Duhem & Buyck (2011)[58]
Nigrohydnum Ryvarden (1987)[59]
Phaeophlebiopsis D.Floudas & Hibbett (2015)[25]
Phlebiella P.Karst. (1890)[60]
Repetobasidiopsis Dhingra & Avn.P.Singh (2008)[61]
Rickiopora Westphalen, Tomšovský & Rajchenb. (2016)[62]
Taiwanofungus Sheng H.Wu, Z.H.Yu, Y.C.Dai & C.H.Su (2004)[63]
Fomitopsis pinicola (Fomitopsidaceae)
Fomitopsis pinicola (Fomitopsidaceae)
Ganoderma lucidum (Ganodermataceae)
Ganoderma lucidum (Ganodermataceae)
Meripilus giganteus (Meripilaceae)
Meripilus giganteus (Meripilaceae)
Podoscypha petalodes (Meruliaceae)
Podoscypha petalodes (Meruliaceae)
Phanerochaete chrysorhizon (Phanerochaetaceae)
Phanerochaete chrysorhizon (Phanerochaetaceae)
Lentinus tigrinus (Polyporaceae)
Lentinus tigrinus (Polyporaceae)
References
Zhao, Chang-Lin; Cui, Bao-Kai; Song, Jie; Dai, Yu-Cheng (2015). "Fragiliporiaceae, a new family of Polyporales (Basidiomycota)". Fungal Diversity. 70 (1): 115–126. doi:10.1007/s13225-014-0299-0. S2CID 7252657.
"Trametales Boidin". MycoBank. International Mycological Association. Retrieved 2016-10-16.
Rea, Carleton (1922). "British Basidiomycetae: A Handbook to the Larger British Fungi". Nature. 111 (2781): 574. Bibcode:1923Natur.111..213B. doi:10.1038/111213a0. S2CID 4123814.
Boidin, J.; Mugnier, J.; Canales, R. (1998). "Taxonomie moleculaire des Aphyllophorales". Mycotaxon (in French). 66: 445–491 (see p. 487).
Gäumann, E. (1926). "Vergleichende Morphologie der Pilze". Nature. 117 (2954): 820. Bibcode:1926Natur.117..820.. doi:10.1038/117820a0. S2CID 4096339.
Corner E.J.H. (1932). "The fruit-body of Polystictus xanthopus, Fr". Annals of Botany. 46 (1): 71–111. doi:10.1093/oxfordjournals.aob.a090319. JSTOR 43237358.
Corner E.J.H. (1932). "A Fomes with two systems of hyphae". Transactions of the British Mycological Society. 17 (1–2): 51–81. doi:10.1016/s0007-1536(32)80026-4.
Corner E.J.H. (1932). "The identification of the brown-root fungus". The Gardens' Bulletin; Straits Settlements. 5: 317–350.
Hawksworth DL, Kirk PM, Sutton BC, Pegler DN, eds. (1995). Dictionary of the Fungi (8th ed.). Wallingford, Oxford: CAB International. ISBN 978-0-85198-885-6.
Justo, Alfredo; Miettinen, Otto; Floudas, Dimitrios; Ortiz-Santana, Beatriz; Sjökvist, Elisabet; Lindner, Daniel; Nakasone, Karen; Niemelä, Tuomo; Larsson, Karl-Henrik; Ryvarden, Leif; Hibbett, David S. (2017). "A revised family-level classification of the Polyporales (Basidiomycota)". Fungal Biology. 121 (9): 798–824. doi:10.1016/j.funbio.2017.05.010. PMID 28800851.
Hibbett DS (2006). "A phylogenetic overview of the Agaricomycotina". Mycologia. 98 (6): 917–925. doi:10.3852/mycologia.98.6.917. PMID 17486968. "Archived copy" (PDF). Archived from the original (PDF) on 2011-07-06. Retrieved 2010-11-01.
Binder M, et al. (2005). "The phylogenetic distribution of resupinate forms across the major clades of mushroom-forming fungi (Homobasidiomycetes)". Systematics and Biodiversity. 3 (2): 113–157. Bibcode:2005SyBio...3..113B. doi:10.1017/s1477200005001623. S2CID 13102957.
Binder, Manfred; Justo, Alfredo; Riley, Robert; Salamov, Asaf; Lopez-Giraldez, Francesc; Sjökvist, Elisabet; Copeland, Alex; Foster, Brian; Sun, Hui; Larsson, Ellen; Larsson, Karl-Henrik; Townsend, Jeffrey; Grigoriev, Igor V.; Hibbett, David S. (2013). "Phylogenetic and phylogenomic overview of the Polyporales". Mycologia. 105 (6): 1350–1373. doi:10.3852/13-003. PMID 23935031. S2CID 20812924.
Garcia-Sandoval, R.; Wang, Z.; Binder, M.; Hibbett, D.S. (2011). "Molecular phylogenetics of the Gloeophyllales and relative ages of clades of Agaricomycotina producing a brown rot". Mycologia. 103 (1): 510–524. doi:10.3852/10-209. PMID 21186327. S2CID 9801943.
Miettinen, Otto; Larsson, Ellen; Sjökvist, Elisabet; Larsson, Karl-Henrik (2012). "Comprehensive taxon sampling reveals unaccounted diversity and morphological plasticity in a group of dimitic polypores (Polyporales, Basidiomycota)". Cladistics. 28 (3): 251–270. Bibcode:2002clad.book.....S. doi:10.1111/j.1096-0031.2011.00380.x. PMID 34872189. S2CID 84643554.
Floudas D, Binder M, Riley R, Barry K, Blanchette RA, Henrissat B, Martínez AT, Otillar R, Spatafora JW, Yadav JS, Aerts A, Benoit I, Boyd A, Carlson A, Copeland A, Coutinho PM, de Vries RP, Ferreira P, Findley K, Foster B, Gaskell J, Glotzer D, Górecki P, Heitman J, Hesse C, Hori C, Igarashi K, Jurgens JA, Kallen N, Kersten P, Kohler A, Kües U, Kumar TK, Kuo A, LaButti K, Larrondo LF, Lindquist E, Ling A, Lombard V, Lucas S, Lundell T, Martin R, McLaughlin DJ, Morgenstern I, Morin E, Murat C, Nagy LG, Nolan M, Ohm RA, Patyshakuliyeva A, Rokas A, Ruiz-Dueñas FJ, Sabat G, Salamov A, Samejima M, Schmutz J, Slot JC, St John F, Stenlid J, Sun H, Sun S, Syed K, Tsang A, Wiebenga A, Young D, Pisabarro A, Eastwood DC, Martin F, Cullen D, Grigoriev IV, Hibbett DS (2012). "The Paleozoic origin of enzymatic lignin decomposition reconstructed from 31 fungal genomes". Science. 336 (6089): 1715–1719. Bibcode:2012Sci...336.1715F. doi:10.1126/science.1221748. hdl:10261/60626. PMID 22745431. S2CID 37121590.
Kendrick, Bryce (2017). The Fifth Kingdom. An Introduction to Mycology (4th ed.). Indianapolis: Hackett Publishing. pp. 124–125. ISBN 978-1-58510-459-8.
"Index Fungorum - Search Page".
Zhou, Li-Wei; Wang, Xue-Wei; Vlasák, Josef; Ren, Guang-Juan (2017). "Resolution of phylogenetic position of Nigrofomitaceae within Hymenochaetales (Basidiomycota) and Nigrofomes sinomelanoporus sp. nov. (Nigrofomitaceae) from China". MycoKeys (29): 1–13. doi:10.3897/mycokeys.29.21250. PMC 5804300. PMID 29559823.Open access icon
Miettinen, Otto; Ryvarden, Leif (2016). "Polypore genera Antella, Austeria, Butyrea, Citripora, Metuloidea and Trulla (Steccherinaceae, Polyporales)". Annales Botanici Fennici. 53 (3–4): 157–172. doi:10.5735/085.053.0403. S2CID 84739655.
Kotiranta, Heikki; Kulju, Matti; Miettinen, Otto (2017). "Caudicicola gracilis (Polyporales, Basidiomycota), a new polypore species and genus from Finland". Annales Botanici Fennici. 54 (1–3): 159–167. doi:10.5735/085.054.0325. hdl:10138/234417. S2CID 90050530.
Volk, Tom (2000). "An introduction to the characters used to identify poroid wood decay fungi". McIlvainea. 14 (2): 74–82.
Alexopoulos, C.J.; Mims, C.W.; Blackwell, M. (1996). Introductory Mycology. New York: Wiley. pp. 570–571. ISBN 978-0-471-52229-4.
Ruiz-Dueñas, Francisco J.; Lundell, Taina; Floudas, Dimitrios; Nagy, Laszlo G.; Barrasa, José M.; Hibbett, David S.; Martínez, Angel T. (2013). "Lignin-degrading peroxidases in Polyporales: an evolutionary survey based on 10 sequenced genomes" (PDF). Mycologia. 105 (6): 1428–1444. doi:10.3852/13-059. hdl:10261/96105. PMID 23921235. S2CID 14165783.
Floudas, D.; Hibbett, D.S. (2015). "Revisiting the taxonomy of Phanerochaete (Polyporales, Basidiomycota) using a four gene dataset and extensive ITS sampling". Fungal Biology. 119 (8): 679–719. doi:10.1016/j.funbio.2015.04.003. PMID 26228559.
Ferreira, Patricia; Carro, Juan; Serrano, Ana; Martínez, Angel T. (2015). "A survey of genes encoding H2O2-producing GMC oxidoreductases in 10 Polyporales genomes". Mycologia (Submitted manuscript). 107 (6): 1105–1119. doi:10.3852/15-027. hdl:10261/132482. PMID 26297778. S2CID 25614887.
de Freitas Soares, Filippe Elias; Sufiate, Bruna Leite; de Queiroz, José Humberto (2018). "Nematophagous fungi: Far beyond the endoparasite, predator and ovicidal groups". Agriculture and Natural Resources. 52: 1–8. doi:10.1016/j.anres.2018.05.010. Open access icon
Reinprecht, Ladislav (2016). Wood Deterioration, Protection and Maintenance. Wiley. p. 147. ISBN 978-1-119-10651-7.
Ulbricht, C.; Weissner, W.; Basch, E.; Giese, N.; Hammerness, P.; Rusie-Seamon, E.; Varghese, M.; Woods, J. (2009). "Maitake mushroom (Grifola frondosa): systematic review by the natural standard research collaboration". J Soc Integr Oncol. 7 (2): 66–72. PMID 19476741.
Lee, Kuo-Hsiung; Morris-Natschke, Susan L.; Yang, Xiaoming; Huang, Rong; Zhou, Ting; Wu, Shou-Fan; Shi, Qian; Itokawa, Hideji (2012). "Recent progress of research on medicinal mushrooms, foods, and other herbal products used in traditional Chinese medicine". Journal of Traditional and Complementary Medicine. 2 (2): 84–95. doi:10.1016/S2225-4110(16)30081-5. PMC 3942920. PMID 24716120.
Lau, B.F.; Abdullah, N.; Aminudin, N.; Lee, H.B.; Tan, P.J. (2015). "Ethnomedicinal uses, pharmacological activities, and cultivation of Lignosus spp. (tiger׳s milk mushrooms) in Malaysia – A review". Journal of Ethnopharmacology. 169: 441–458. doi:10.1016/j.jep.2015.04.042. PMID 25937256.
Slaven, Zjalic; Adele, Fabbri Anna; Alessandra, Ricelli; Corrado, Fanelli; Massimo, Reverberi (2008). "Medicinal mushrooms". In Ray, Ramesh C.; Ward, Owen P. (eds.). Microbial Biotechnology in Horticulture. CRC Press. p. 308. ISBN 978-1-57808-520-0.
Grienke, Ulrike; Zöll, Margit; Peintner, Ursula; Rollinger, Judith M. (2016). "European medicinal polypores—a modern view on traditional uses". Journal of Ethnopharmacology. 154 (3): 564–583. doi:10.1016/j.jep.2014.04.030. PMID 24786572.
Kuo, Michael (2007). 100 Edible Mushrooms. Ann Arbor, Michigan: The University of Michigan Press. pp. 79–84, 108–110. ISBN 978-0-472-03126-9.
Newton, John (2016). The Oldest Foods on Earth: A History of Australian Native Foods with Recipes. NewSouth. p. 29. ISBN 978-1-74224-226-2.
Lau, Beng Fye; Abdullah, Noorlidah (2017). "Bioprospecting of Lentinus squarrosulus Mont., an underutilized wild edible mushroom, as a potential source of functional ingredients: A review". Trends in Food Science & Technology. 61: 116–131. doi:10.1016/j.tifs.2016.11.017.
McLean, Robert Colquhoun; Cook, Walter Robert Ivimey (1951). Textbook of Theoretical Botany. Longmans, Green. p. 317. ISBN 9780470585580.
Pegler D. (2001). "Useful fungi of the world: Amadou and Chaga". Mycologist. 15 (4): 153–154. doi:10.1016/S0269-915X(01)80004-5. "In Germany, this soft, pliable 'felt' has been harvested for many years for a secondary function, namely in the manufacture of hats, dress adornments and purses."
Blanchette, Robert A. (1997). "Haploporus odorus: a sacred fungus in traditional native American culture of the northern plains". Mycologia. 89 (2): 233–240. doi:10.2307/3761076. JSTOR 3761076.
Bessette, Alan; Bessette, Arleen Rainis (2001). The Rainbow Beneath my Feet: A Mushroom Dyer's Field Guide. Syracuse, New York: Syracuse University Press. p. 96. ISBN 978-0-8156-0680-2.
Chen S, Xu J, Liu C, Zhu Y, Nelson DR, Zhou S, Li C, Wang L, Guo X, Sun Y, Luo H, Li Y, Song J, Henrissat B, Levasseur A, Qian J, Li J, Luo X, Shi L, He L, Xiang L, Xu X, Niu Y, Li Q, Han MV, Yan H, Zhang J, Chen H, Lv A, Wang Z, Liu M, Schwartz DC, Sun C (2012). "Genome sequence of the model medicinal mushroom Ganoderma lucidum". Nature Communications. 3 (1): 913. Bibcode:2012NatCo...3..913C. doi:10.1038/ncomms1923. PMC 3621433. PMID 22735441.
Yap, H.Y.; Chooi, Y.H.; Firdaus-Raih, M.; Fung, S.Y.; Ng, S.T.; Tan, C.S.; Tan, N.H. (2014). "The genome of the Tiger Milk mushroom, Lignosus rhinocerotis, provides insights into the genetic basis of its medicinal properties". BMC Genomics. 15 (1): 635. doi:10.1186/1471-2164-15-635. PMC 4129116. PMID 25073817.
Martinez D, Larrondo LF, Putnam N, Gelpke MD, Huang K, Chapman J, Helfenbein KG, Ramaiya P, Detter JC, Larimer F, Coutinho PM, Henrissat B, Berka R, Cullen D, Rokhsar D (2004). "Genome sequence of the lignocellulose degrading fungus Phanerochaete chrysosporium strain RP78". Nature Biotechnology. 22 (6): 695–700. doi:10.1038/nbt967. PMID 15122302.
Martinez D, Challacombe J, Morgenstern I, Hibbett D, Schmoll M, Kubicek CP, Ferreira P, Ruiz-Duenas FJ, Martinez AT, Kersten P, Hammel KE, Vanden Wymelenberg A, Gaskell J, Lindquist E, Sabat G, Bondurant SS, Larrondo LF, Canessa P, Vicuna R, Yadav J, Doddapaneni H, Subramanian V, Pisabarro AG, Lavín JL, Oguiza JA, Master E, Henrissat B, Coutinho PM, Harris P, Magnuson JK, Baker SE, Bruno K, Kenealy W, Hoegger PJ, Kües U, Ramaiya P, Lucas S, Salamov A, Shapiro H, Tu H, Chee CL, Misra M, Xie G, Teter S, Yaver D, James T, Mokrejs M, Pospisek M, Grigoriev IV, Brettin T, Rokhsar D, Berka R, Cullen D (2009). "Genome, transcriptome, and secretome analysis of wood decay fungus Postia placenta supports unique mechanisms of lignocellulose conversion". Proceedings of the National Academy of Sciences USA. 106 (6): 1954–1959. Bibcode:2009PNAS..106.1954M. doi:10.1073/pnas.0809575106. PMC 2644145. PMID 19193860.
Kameshwar, Ayyappa Kumar Sista; Qin, Wensheng (2017). "Metadata Analysis of Phanerochaete chrysosporium gene expression data identified common CAZymes encoding gene expression profiles involved in cellulose and hemicellulose degradation". International Journal of Biological Sciences. 13 (1): 85–99. doi:10.7150/ijbs.17390. PMC 5264264. PMID 28123349.
Vanden Wymelenberg A.; Jill Gaskell; Michael Mozuch; Grzegorz Sabat; John Ralph; Oleksandr Skyba; Shawn D. Mansfield; Robert A. Blanchette; Diego Martinez; Igor Grigoriev; Philip J. Kersten; Dan Cullen (2010). "Comparative transcriptome and secretome analysis of wood decay fungi Postia placenta and Phanerochaete chrysosporium". Applied and Environmental Microbiology. 76 (11): 3599–3610. Bibcode:2010ApEnM..76.3599V. doi:10.1128/AEM.00058-10. PMC 2876446. PMID 20400566.
Brown, Roland W. (1940). "A bracket fungus from the late Tertiary of southwestern Idaho". Journal of the Washington Academy of Sciences. 30 (10): 422–424. JSTOR 24529677.
Fleischmann, Andreas; Krings, Michael; Mayr, Helmut; Agerer, Reinhard (2007). "Structurally preserved polypores from the Neogene of North Africa: Ganodermites libycus gen. et sp. nov. (Polyporales, Ganodermataceae)". Review of Palaeobotany and Palynology. 145 (1–2): 159–172. Bibcode:2007RPaPa.145..159F. doi:10.1016/j.revpalbo.2006.10.001.
Zhao, Rui-Lin; Li, Guo-Jie; Sánchez-Ramírez, Santiago; Stata, Matt; Yang, Zhu-Liang; Wu, Gang; Dai, Yu-Cheng; He, Shuang-Hui; Cui, Bao-Kai; Zhou, Jun-Liang; Wu, Fang; He, Mao-Qiang; Moncalvo, Jean-Marc (2017). "A six-gene phylogenetic overview of Basidiomycota and allied phyla with estimated divergence times of higher taxa and a phyloproteomics perspective". Fungal Diversity. 84 (1): 43–74. doi:10.1007/s13225-017-0381-5. S2CID 1864841.
Gómez-Montoya, N.; Rajchenberg, M.; Robledo, G.L. (2017). "Aegis boa (Polyporales, Basidiomycota) a new neotropical genus and species based on morphological data and phylogenetic evidences". Mycosphere. 8 (6): 1261–1269. doi:10.5943/mycosphere/8/6/11. hdl:11336/45986. Open access icon
Karasiński, Dariusz; Niemelä, Tuomo (2016). "Anthoporia, a new genus in the Polyporales (Agaricomycetes)" (PDF). Polish Botanical Journal. 61 (1): 7–14. doi:10.1515/pbj-2016-0017. Open access icon
Duhem, Bernard; Schultheis, Ben (2011). "Bourdotiella complicata gen. et sp. nov. de France". Cryptogamie, Mycologie (in French). 32 (4): 391–401. doi:10.7872/crym.v32.iss4.2011.391. S2CID 84992028.
Hjortstam K, Ryvarden L (2005). "New taxa and new combinations in tropical corticioid fungi, (Basidiomycotina, Aphyllophorales)". Synopsis Fungorum. 20: 33–41.
Qin, Wen-Min; Wu, Fang; Zhou, Li-Wei (2016). "Donkioporiella mellea gen. et sp. nov. (Polyporales, Basidiomycota) from Guangxi, China". Cryptogamie, Mycologie. 37 (4): 437–447. doi:10.7872/crym/v37.iss4.2016.437. S2CID 89715790.
Jülich W. (1980). "Notulae et novitates Muluenses". Botanical Journal of the Linnean Society. 81: 43–6. doi:10.1111/j.1095-8339.1980.tb00940.x.
Hjortstam K, Ryvarden L (2004). "Some new tropical genera and species of corticioid fungi (Basidiomycotina, Aphyllophorales)". Synopsis Fungorum. 18: 20–32.
Rick, J. (1940). "Resupinati Riograndenses II". Annales Mycologici. 38 (1): 56–60.
Duhem, Bernard; Buyck, Bart (2011). "Meruliophana mahorensis gen. et sp. nov. de l'île de Mayotte (France Outre-Mer)". Cryptogamie, Mycologie. 32 (2): 135–143. doi:10.7872/crym.v32.iss2.2011.135. S2CID 86045350.
Ryvarden L. (1987). "New and noteworthy polypores from tropical America". Mycotaxon. 28 (2): 525–41 (see p. 532).
Karsten, P.A. (1890). "Fragmenta mycologica XXXI". Hedwigia (in Latin). 29: 270–273.
Dhingra, G.S.; Singh, Avneet P. (2008). "Validation of Repetobasidiopsis and Trimitiella (Basidiomycetes)". Mycotaxon. 105: 421–422.
Westphalen, Mauro C.; Rajchenberg, Mario; Tomšovský, Michal; Gugliotta, Adriana M. (2016). "Extensive characterization of the new genus Rickiopora (Polyporales)". Fungal Biology. 120 (8): 1002–1009. doi:10.1016/j.funbio.2016.05.001. PMID 27521631.
Wu SH, Yu ZH, Dai YC, Chen CT, Su CH, Chen LC, Hsu WC, Hwang GY (2004). "Taiwanofungus, a polypore new genus". Fungal Science (in Chinese). 19 (3–4): 109–116.
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