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Fungal diversity notes 491–602: taxonomic and phylogenetic contributions to fungal taxa

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Abstract

This is a continuity of a series of taxonomic and phylogenetic papers on the fungi where materials were collected from many countries, examined and described. In addition to extensive morphological descriptions and appropriate asexual and sexual connections, DNA sequence data are also analysed from concatenated datasets to infer phylogenetic relationships and substantiate systematic positions of taxa within appropriate ranks. Wherever new species or combinations are proposed, we apply an integrative approach using morphological and molecular data as well as ecological features wherever applicable. Notes on 112 fungal taxa are compiled in this paper including Biatriosporaceae and Roussoellaceae, Didysimulans gen. nov., 81 new species, 18 new host records and new country records, five reference specimens, two new combinations, and three sexual and asexual morph reports. The new species are Amanita cornelii, A. emodotrygon, Angustimassarina alni, A. arezzoensis, A. italica, A. lonicerae, A. premilcurensis, Ascochyta italica, A. rosae, Austroboletus appendiculatus, Barriopsis thailandica, Berkleasmium ariense, Calophoma petasitis, Camarosporium laburnicola, C. moricola, C. grisea, C. ossea, C. paraincrustata, Colletotrichum sambucicola, Coprinopsis cerkezii, Cytospora gelida, Dacrymyces chiangraiensis, Didysimulans italica, D. mezzanensis, Entodesmium italica, Entoloma magnum, Evlachovaea indica, Exophiala italica, Favolus gracilisporus, Femsjonia monospora, Fomitopsis flabellata, F. roseoalba, Gongronella brasiliensis, Helvella crispoides, Hermatomyces chiangmaiensis, H. chromolaenae, Hysterium centramurum, Inflatispora caryotae, Inocybe brunneosquamulosa, I. luteobrunnea, I. rubrobrunnea, Keissleriella cirsii, Lepiota cylindrocystidia, L. flavocarpa, L. maerimensis, Lophiotrema guttulata, Marasmius luculentus, Morenoina calamicola, Moelleriella thanathonensis, Mucor stercorarius, Myrmecridium fluviae, Myrothecium septentrionale, Neosetophoma garethjonesii, Nigrograna cangshanensis, Nodulosphaeria guttulatum, N. multiseptata, N. sambuci, Panus subfasciatus, Paraleptosphaeria padi, Paraphaeosphaeria viciae, Parathyridaria robiniae, Penicillium punicae, Phaeosphaeria calamicola, Phaeosphaeriopsis yuccae, Pleurophoma italica, Polyporus brevibasidiosus, P. koreanus, P. orientivarius, P. parvovarius, P. subdictyopus, P. ulleungus, Pseudoasteromassaria spadicea, Rosellinia mearnsii, Rubroboletus demonensis, Russula yanheensis, Sigarispora muriformis, Sillia italica, Stagonosporopsis ailanthicola, Strobilomyces longistipitatus, Subplenodomus galicola and Wolfiporia pseudococos. The new combinations are Melanomma populina and Rubroboletus eastwoodiae. The reference specimens are Cookeina tricholoma, Gnomoniopsis sanguisorbae, Helvella costifera, Polythrincium trifolii and Russula virescens. The new host records and country records are Ascochyta medicaginicola, Boletellus emodensis, Cyptotrama asprata, Cytospora ceratosperma, Favolaschia auriscalpium, F. manipularis, Hysterobrevium mori, Lentinus sajor-caju, L. squarrosulus, L. velutinus, Leucocoprinus cretaceus, Lophiotrema vagabundum, Nothophoma quercina, Platystomum rosae, Pseudodidymosphaeria phlei, Tremella fuciformis, Truncatella spartii and Vaginatispora appendiculata and three sexual and asexual morphs are Aposphaeria corallinolutea, Dothiora buxi and Hypocrella calendulina.

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References

  • Aalto M (1974) Amanita magnivolvata sp. nova (Agaricales). Karstenia 14:93–96

    Google Scholar 

  • Abbott SP, Currah RS (1997) The Hevellaceae: systematic revision and occurrence in northern and northwestern North America. Mycotaxon 62:1–125

    Google Scholar 

  • Abdollahzadeh J, Goltapeh EM, Javadi A, Shams-Bakhsh M, Zare R, Phillips AJL (2009) Barriopsis iraniana and Phaeobotryon cupressi, two new species of the Botryosphaeriaceae from trees in Iran. Persoonia 23:1–8

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Adamčík S, Cai L, Chakraborty D, Chen XH, Cotter H, Van T, Dai DQ, Dai YC, Sas K, Deng C, Ghobad-Nejhad M, Hyde KD, Langer E, Latha KPD, Liu F, Liu SL, Liu T, Wei LV, Shu-Xia LV, Machado AR, Pinho DB, Pereira OL, Prasher IB, Rosado AWC, Qin J, Qin WM, Verma RK, Wang Q, Yang ZL, Yu XD, Zhou LW, Buyck B (2015) Fungal biodiversity profiles 1–10. Cryptogam Mycol 36:121–166

    Article  Google Scholar 

  • Adams GC, Wingfield MJ, Common R, Roux J (2005) Phylogenetic relationships and morphology of Cytospora species and related teleomorphs (Ascomycota, Diaporthales, Valsaceae) from Eucalyptus. Stud Mycol 52:1–144

    Google Scholar 

  • Adams GC, Roux J, Wingfield MJ (2006) Cytospora species (Ascomycota, Diaporthales, Valsaceae): introduced and native pathogens of trees in South Africa. Australas Plant Pathol 35:521–548

    Article  Google Scholar 

  • Addy HD, Piercey MM, Currah RS (2005) Microfungal endophytes in roots. Can J Bot 83:1–13

    Article  Google Scholar 

  • Ahmad S (1969) Fungi of West Pakistan, supplement 1. Society at the Biological Laboratories, Government College, Lahore

    Google Scholar 

  • Ahmad S, Iqbal SH, Khalid AN (1997) Fungi of Pakistan. Sultan Ahmad Mycological Society of Pakistan, Department of Botany, University of the Punjab, Lahore

    Google Scholar 

  • Aime L, Ryvarden L, Henkel TW (2007) Studies in Neotropicalpolypores 22. Additional new and rare species from Guyana. Synop Fungorum 23:15–31

    Google Scholar 

  • Alvarado P, Manjon JL, Matheny PB, Esteve-Raventos F (2010) Tubariomyces, a new genus of Inocybaceae from the Mediterranean region. Mycologia 102:1389–1397

    Article  PubMed  Google Scholar 

  • Andersson M (2013) A rare bolete, Boletus legaliae, in the Royal Garden of Drottningholm, Stockholm. Sven Mykol Tidskr 34(3):9–13

    Google Scholar 

  • Antonín V, Buyck B (2006) Marasmius (Basidiomycota, Marasmiaceae) in Madagascar and the Mascarenes. Fungal Divers 23:17–50

    Google Scholar 

  • Antonín V (2007) Monograph of Marasmius, Gloiocephala, Palaeocephala and Setulipes in tropical Africa. Fungus Flora Trop Afr 1:1–177

    Google Scholar 

  • Antonín V, Vizzini A, Ercole E, Leonardi M (2015) Strobilomyces pteroreticulosporus (Boletales), a new species of the S. strobilaceus complex from the Republic of Korea and remarks on the variability of S. confuses. Phytotaxa 219(1):78–86

    Article  Google Scholar 

  • Ariyawansa HA, Tanaka K, Thambugala KM, Phookamsak R, Tian Q, Camporesi E, Hongsanan S, Monkai J, Wanasinghe DN, Mapook A, Chukeatirote E (2014a) A molecular phylogenetic reappraisal of the Didymosphaeriaceae (=Montagnulaceae). Fungal Divers 68:69–104

    Article  Google Scholar 

  • Ariyawansa HA, Hawksworth DL, Hyde KD, Jones EG, Maharachchikumbura SS, Manamgoda DS, Thambugala KM, Udayanga D, Camporesi E, Daranagama A, Jayawardena R (2014b) Epitypification and neotypification: guidelines with appropriate and inappropriate examples. Fungal Divers 69(1):57–91

    Article  Google Scholar 

  • Ariyawansa HA, Phukhamsakda C, Thambugala KM, Bulgakov TS, Wanasinghe DN, Perera RH, Mapook A, Camporesi E, Kang JC, Jones EG, Bahkali AH (2015a) Revision and phylogeny of Leptosphaeriaceae. Fungal Divers 74:19–51

    Article  Google Scholar 

  • Ariyawansa HA, Thambugala KM, Manamgoda DS, Jayawardena R, Camporesi E, Boonmee S, Wanasinghe DN, Phookamsak R, Hongsanan S, Singtripop C, Chukeatirote E (2015b) Towards a natural classification and backbone tree for Pleosporaceae. Fungal Divers 71(1):85–139

    Article  Google Scholar 

  • Ariyawansa HA, Hyde KD, Jayasiri SC, Buyck B, Chethana KWT, Dai DQ, Dai YC, Daranagama DA, Jayawardena RS, Lücking R, Ghobad-Nejhad M, Niskanen T, Thambugala KM, Voigt K, Zhao RL, Li GJ, Doilom M, Boonmee S, Yang ZL, Cai Q, Cui YY, Bahkali AH, Chen J, Cui BK, Chen JJ, Dayarathne MC, Dissanayake AJ, Ekanayaka AH, Hashimoto A, Hongsanan S, Jones EBG, Larsson E, Li WJ, Li QR, Liu JK, Luo ZL, Maharachchikumbura SSN, Mapook A, McKenzie EHC, Norphanphoun C, Konta S, Pang KL, Perera RH, Phookamsak R, Phukhamsakda C, Pinruan U, Randrianjohany E, Singtripop C, Tanaka K, Tian CM, Tibpromma S, Abdel-Wahab MA, Wanasinghe DN, Wijayawardene NN, Zhang JF, Zhang H, Abdel- Aziz FA, Wedin M, Westberg M, Ammirati JF, Bulgakov TS, Lima DX, Callaghan TM, Callac P, Chang CH, Coca LF, Dal-Forno M, Dollhofer V, Fliegerová K, Greiner K, Griffith GW, Ho HM, Hofstetter V, Jeewon R, Kang JC, Wen TC, Kirk PM, Kytövuori I, Lawrey JD, Xing J, Li H, Liu ZY, Liu XZ, Liimatainen K, Thorsten Lumbsch H, Matsumura M, Moncada B, Nuankaew S, Parnmen S, Santiago ALCMA, Sommai S, Song Y, de Souza CAF, de Souza- Motta CM, Su HY, Suetrong S, Wang Y, FongWS YH, Zhou LW, Réblová M, Fournier J, Camporesi E, Luangsa-ard JJ, Tasanathai K, Khonsanit A, Thanakitpipattana D, Somrithipol S, Diederich P, Millanes AM, Common RS, Stadler M, Yan JY, Li XH, Lee HW, Nguyen TTT, Lee HB, Battistin E, Marsico O, Vizzini A, Vila J, Ercole E, Eberhardt U, Simonini G, Wen HA, Chen XH, Miettinen O, Spirin V, Hernawati (2015c) Fungal diversity notes 111–252 taxonomic and phylogenetic contributions to fungal taxa. Fungal Divers 75:27–274

    Article  Google Scholar 

  • Arora D, Ferrarese G, Simonini G (1999) Boletus pulcherrimus Boletus rubrosanguineus: lo stesso taxon? Micol Veget Medit 14(2):116–141

    Google Scholar 

  • Arun Kumar TK, Manimohan P (2009) The genus Lepiota (Agaricales, Basidiomycota) in Kerala State, India. Mycotaxon 107:105–138

    Article  Google Scholar 

  • Arzanlou M, Groenewald JZ, Gams W, Braun U, Shin HD, Crous PW (2007) Phylogenetic and morphotaxonomic revision of Ramichloridium and allied genera. Stud Mycol 58:57–93

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Aveskamp MM, de Gruyter J, Crous PW (2008) Biology and recent developments in the systematics of Phoma, a complex genus of major quarantine significance. Fungal Divers 31:1–18

    Google Scholar 

  • Aveskamp MM, de Gruyter J, Woudenberg JHC, Verkley GJM, Crou PW (2010) Highlights of the Didymellaceae: a polyphasic approach to characterise Phoma and related pleosporalean genera. Stud Mycol 65:1–60

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bahl J, Jeewon R, Hyde KD (2005) Phylogeny of Rosellinia capetribulensis sp. nov. and its allies (Xylariaceae). Mycologia 97:1102–1110

    Article  CAS  PubMed  Google Scholar 

  • Baroni TJ, Hofstetter V, Largent DL, Vilgalys R (2011) Entocybe is proposed as a new genus in the Entolomataceae (Agaricomycetes, Basidiomycota) based on morphological and molecular evidence. N Am Fungi 6:1–19

    Google Scholar 

  • Barr ME (1978) The Diaporthales in North America with emphasis on Gnomonia and its segregates. Mycol Mem 7:1–232

    Google Scholar 

  • Barr ME (1979) A classification of Loculoascomycetes. Mycologia 71:935–957

    Article  Google Scholar 

  • Barr ME (1987) Prodomus to class Loculoascomycetes. Published by the Author, Amherst

    Google Scholar 

  • Barr ME (1990) Melanommatales (Loculoascomycetes). N Am Flora Ser II 13:1–129

    Google Scholar 

  • Barr ME (1992) Notes on the Lophiostomataceae (Pleosporales). Mycotaxon 45:191–221

    Google Scholar 

  • Bas C (1969) Morphology and subdivision of Amanita and a monograph of its section Lepidella. Persoonia 5:285–579

    Google Scholar 

  • Bas C (1974) A rare and widespread Amanita associated with Alnus. Bulletin Mensuel de la Société Linnéenne de Lyon 43:17–23

    Article  Google Scholar 

  • Bas C (1984) On the correct name of ‘Amanita inaurata Secr.’. Persoonia Mol Phylogeny Evol Fungi 12:192–193

    Google Scholar 

  • Bas C, Kuyper TW, Noordeloos ME, Vellinga EC (1995) Flora Agaricina Neerlandica—3, Tricholomataceae. A. A. Balkema, Rotterdam

  • Bates ST, Reddy GSN, Garcia-Pichel F (2006) Exophiala crusticola anam. nov. (affinity Herpotrichiellaceae), a novel black yeast from biological soil crusts in the Western United States. Int J Syst Evol Microbiol 56:2697–2702

    Article  CAS  PubMed  Google Scholar 

  • Bau T, Li Y, Irina AG, Eugenia MB, Wasiliy AS (2008) Common wild edible mushroom resource of Russia. Edible Fungi China 27:9–13

    Google Scholar 

  • Benny GL (2008) Methods used by Dr. R. K. Benjamin, and other mycologists, to isolate Zygomycetes. Aliso 26:37–61

    Article  Google Scholar 

  • Benny GL, Smith ME, Kirk PM, Tretter ED, White MM (2016) Challenges and Future Perspectives in the Systematics of Kickxellomycotina, Mortierellomycotina, Mucoromycotina, and Zoopagomycotina. In: Li D-W (ed) Biology of microfungi, fungal biology. Springer, Basel

    Google Scholar 

  • Berkeley MJ (1847) Decades of fungi XII–XIV. Lond J Bot 6:312–326

    Google Scholar 

  • Bernicchia A, Gorjón SP (2010) Corticiaceae s.l. Fungi Europaei, vol 12. Ed Candusso, Italia

  • Bessette AE, Roody WC, Bessette AR (2000) North American Boletes. Syracuse University Press, Syracuse

    Google Scholar 

  • Bessette AE, Roody WC, Bessette AR (2010) North American Boletes: a color guide to fleshy pored mushrooms. Syracuse University Press, Syracuse

    Google Scholar 

  • Bhatt RP, Tulloss RE, Semwal KC, Bhatt VK, Moncalvo JM, Stephenson SL (2003) Amanitaceae from India. A critically annotated checklist. Mycotaxon 88:249–270

    Google Scholar 

  • Binder M, Hibbett DS (2006) Molecular systematics and biological diversification of Boletales. Mycologia 98:971–981

    Article  PubMed  Google Scholar 

  • Binder M, Justo A, Riley R, Salamov A, Lopez-Giraldez F, Sjökvist E, Copeland A, Foster B, Sun H, Larsson E, Larsson KH, Townsend J, Grigoriev IV, Hibbett D (2013) Phylogenetic and phylogenomic overview of the Polyporales. Mycologia 105:1350–1373

    Article  CAS  PubMed  Google Scholar 

  • Binion DE, Stephenson SL, Roody WC, Burdsall HH Jr., Vasilyeva LN, Miller OK Jr. (2008) Macrofungi associated with oaks of Eastern North America. West Virginia University Press, Morgantown

    Google Scholar 

  • Bisby GR, Buller AHR, Dearness J (1929) The fungi of Manitoba. Longmans, Green and Co, London

    Google Scholar 

  • Boehm EW, Schoch CL, Spatafora JW (2009a) On the evolution of the Hysteriaceae and Mytilinidiaceae (Pleosporomycetidae, Dothideomycetes, Ascomycota) using four nuclear genes. Mycol Res 113:461–479

    Article  CAS  PubMed  Google Scholar 

  • Boehm EWA, Mugambi G, Miller AN, Huhndorf S, Marincowitz S, Schoch CL, Spatafora JW (2009b) A molecular phylogenetic reappraisal of the Hysteriaceae, Mytilinidiaceae and Gloniaceae (Pleosporomycetidae, Dothideomycetes) with keysto world species. Stud Mycol 64:49–83

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bolay A (1971) Contribution a la connaissance de Gnomonia comari Karsten (syn. G. fructicola [Arnaud] Fall). Etude taxonomique, phytopathologique et recherches sur sa croissance in vitro. Ber Schweizerischen Bot Ges 81:398–482

    Google Scholar 

  • Borisov BA, Tarasov KL (1999) Notes on biodiversity of causal agents of invertebrate mycoses in Adjaria (south-western Georgia). I. Evlachovaea kintrischica gen. et sp. nov. (Hyphomycetes) from Kintrishi Reservation. Mikologiya i Fitopatologiya 33(4):248–256

    Google Scholar 

  • Breitenbach J, Kränzlin F (1991) Fungi of Switzerland, vol. 3, Boletes and Agarics 1st part. Mykologia, Lucerne, Switzerland

  • Bresadola J (1896) Fungi Tridentini. 195 plates. 1881–1900. Contains figures of Hydnaceae. Fungi Brasilienses. Hedwigia 35:276–302

    Google Scholar 

  • Bukovská P, Jelínková M, Hršelová H, Sýkorová Z, Gryndler M (2010) Terminal restriction fragment length measurement errors are affected mainly by fragment length, G+C nucleotide content and secondary structure melting point. J Microbiol Methods 82:223–228

    Article  PubMed  CAS  Google Scholar 

  • Bussaban B, Lumyong S, Lumyong P, Mckenzie EHC, Hyde KD (2001) A synopsis of the genus Berkleasmium with two new species and new records of Canalisporium caribense from Zingiberaceae in Thailand. Fungal Divers 8:73–85

    Google Scholar 

  • Buyck B, Hofstetter V, Eberhardt U, Verbeken A, Kauff F (2008) Walking the thin line between Russula and Lactarius: the dilemma of Russula subsect. Ochricompactae. Fungal Divers 28:15–40

    Google Scholar 

  • Buyck B, Hofstetter V, Verbeken A, Walleyn R (2010) (1919) Proposal to conserve Lactarius nom. cons. (Basidiomycota) with a conserved type. Taxon 59(1):295–296

    Google Scholar 

  • Cai L, Jeewon R, Hyde KD (2006) Phylogenetic investigations of Sordariaceae based on multiple gene sequences and morphology. Mycol Res 110:137–150

    Article  CAS  PubMed  Google Scholar 

  • Calzada Dominguez A (2007) Guía de los Boletos de España y Portugal. Náyade Editorial, Medina del Campo, Valladolid

  • Câmara MPS, Palm ME, van Berkum P, O’Neill NR (2002) Molecular phylogeny of Leptosphaeria and Phaeosphaeria. Mycologia 94:630–640

    Article  PubMed  Google Scholar 

  • Câmara MP, Ramaley AW, Castlebury LA, Palm ME (2003) Neophaeosphaeria and Phaeosphaeriopsis, segregates of Paraphaeosphaeria. Mycol Res 107:516–522

    Article  PubMed  Google Scholar 

  • Cannon PF, Kirk PM (2007) Fungal families world, 7th edn. CAB International, Wallingford

    Google Scholar 

  • Cannon PF, Hawksworth DL, Sherwood-Pike MA (1985) The British Ascomycotina. An annotated checklist. Commonwealth Mycological Institute, Kew, Surrey

    Google Scholar 

  • Cannon PF, Damm U, Johnston PR, Weir BS (2012) Colletotrichum current status and future directions. Study Mycol 73:181–213

    Article  CAS  Google Scholar 

  • Carbone I, Kohn LM (1999) A method for designing primer sets for speciation studies in filamentous ascomycetes. Mycologia 91:553–556

    Article  CAS  Google Scholar 

  • Carmichael JW (1966) Cerebral mycetoma of trout due to a Phialophora-like fungus. Sabouraudia 6:120–123

    Google Scholar 

  • Carmichael JW (1967) Cerebral mycetoma of trout due to a Phialophora-like fungus. Sabouraudia. J Med Vet Mycol 5(2):120–123

    Article  Google Scholar 

  • Carson ML (2005) Yield loss potential of Phaeosphaeria leaf spot of maize caused by Phaeosphaeria maydis in the United States. Plant Dis 89:986–988

    Article  Google Scholar 

  • Castañeda RF, Heredia G (2000) Two new dematiaceous hyphomycetes on Cyathea from Mexico. Cryptogam Mycol 21:221–228

    Article  Google Scholar 

  • Castlebury LA, Rossman AY, Jaklitsch WJ, Vasilyeva LN (2002) A preliminary overview of the Diaporthales based on large subunit nuclear ribosomal DNA sequences. Mycologia 94:1017–1031

    Article  CAS  PubMed  Google Scholar 

  • Chaverri P, Bischoff JF, Evans HC, Hodge KT (2005) Regiocrella a new entomopathogenic genus with a pycnidial anamorph and its phylogenetic placement in the Clavicipitaceae. Mycologia 97:1225–1237

    Article  PubMed  Google Scholar 

  • Chaverri P, Liu M, Hodge KT (2008) A monograph of the entomopatho- genic genera Hypocrella, Moelleriella and Samuelsia gen. nov. (Ascomycota, Hypocreales, Clavicipitaceae) and their aschersonia-like anamorphs in the Neotropics. Stud Mycol 60:1–66

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Checa J, Ramaley AW, Palm-Hernández ME, Câmara MP (2002) Paraphaeosphaeria barrii, a new species on Yucca schidigera from Mexico. Mycol Res 106:375–379

    Article  Google Scholar 

  • Cheewangkoon R, Crous PW, Hyde KD, Groenewald JZ, To-Anan C (2008) Species of Mycosphaerella and related anamorphs on Eucalyptus leaves from Thailand. Persoonia 21:77–91

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Chen Q, Jiang JR, Zhang GZ, Cai L, Crous PW (2015) Resolving the Phoma enigma. Stud Mycol 82:137–217

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Chen Y, Ran SF, Dai DQ, Wang Y, Hyde KD, Wu YM, Jiang YL (2016) Mycosphere Essays 2. Myrothecium. Mycosphere 7:64–80

    Google Scholar 

  • Chen ZH, Zhang P, Zhang ZG (2013) Investigation and analysis of 102 mushroom poisoning cases in southern China from 1994 to 2012. Fungal Divers 64:123–131

    Article  Google Scholar 

  • Chethana KWT, Phillips AJL, Zhang W, Chen Z, Hao YY, Hyde KD, Li XH, Yan JY (2016) Mycosphere Essays 5: Is it important to name species of Botryosphaeriaceae? Mycosphere 7:870–882

    Google Scholar 

  • Chevallier FF (1826) Flore Générale des Environs de Paris [General Flora of the Area Around Paris]. Ferra Jeune, France, pp 1–674

  • Cheype JL (1983) Validation de Boletus rubrosanguineus (Walty). Doc Mycol 52:53–54

    Google Scholar 

  • Chlebicki A, Mukhin VA, Ushakowa N (2003) Fomitopsisofficinalis on Siberian Larch in Urals. Mycologist 17:116–120

    Article  Google Scholar 

  • Chomnunti P, Schoch CL, Aguirre-Hudson B, KoKo TW, Hongsanan S, Jones EBG, Kodsub R, Chukeatirote E, Bahkali AH, Hyde KD (2011) Capnodiaceae. Fungal Divers 51:103–134

    Article  PubMed  PubMed Central  Google Scholar 

  • Chomnunti P, Hongsanan S, Hudson BA, Tian Q, Peršoh D, Dhami MK, Alias AS, Xu J, Liu X, Stadler M, Hyde KD (2014) The sooty moulds. Fungal Divers 66:1–36

    Article  Google Scholar 

  • Chouhan JS, Panwar KS (1980) Hyphomycetes of Mount Abu-V. Indian Phytopathol 33:285–291

    Google Scholar 

  • Clements FE, Shear CL (1931) Genera of fungi, 2nd edn. H.W. Wilson, New York

    Google Scholar 

  • Co-David D, Langeveld D, Noordeloos ME (2009) Molecular phylogeny and spore evolution of Entolomataceae. Persoonia 23:147–176

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Consiglio G, Simonini G (2005) Trattamento statistico delle dimensioni sporali. In: Consiglio G, Antonini D, Antonini M (eds) Il Genere Cortinarius, parte III. Centro Studi Micologici AMB, pp 33–44

  • Corda ACI (1831) Die Pilze Deutschlands. In: Sturm J (ed) Deutschlands Flora in Abbildungen nach der Natur mit Beschreibungen, vol 12(3). Sturm, Nurnberg, pp 33–64

  • Corda ACJ (1837) Icones fungorum hucusque cognitorum, vol 1. J.G. Calve, Prague

    Google Scholar 

  • Corlett M (1981) A taxonomic survey of some species of Didymella and Didymella-like species. Can J Bot 59:2016–2042

    Article  Google Scholar 

  • Corner EJH (1950) A monograph of Clavaria and allied genera. Oxford University Press, Oxford

    Google Scholar 

  • Corner EJH (1970) Supplement to a monograph of Clavaria and allied genera. Beihefte zur Nova Hedwigia 33:1–299

    Google Scholar 

  • Corner EJH (1981) The agaric genera Lentinus, Panus, and Pleurotus with particular reference to Malaysian species. Nova Hedwigia 69:1–169

    Google Scholar 

  • Corner EJH (1996) The agaric genera Marasmius, Chaetocalathus, Crinipellis, Heimiomyces, Resupinatus, Xerula and Xerulina in Malesia. Beih Nova Hedwigia 111:1–175

    Google Scholar 

  • Corner EJH, Thind KS, Anand GPS (1956) The Clavariaceae of the Mussoorie hills (India). II. Trans Br Mycol Soc 39(4):475–484

    Article  Google Scholar 

  • Courtecuisse R, Duhem B (2011) Guide des Champignons de France et d’Europe. Delachaux et Niestlé, Paris

  • Cripps CL (1997) The genus Inocybe in Montana aspen stands. Mycologia 89:670–688

    Article  Google Scholar 

  • Crous PW, Braun U (2003) Mycosphaerella and its anamorphs: 1. Names published in Cercospora and Passalora. CBS biodiversity series no Centraalbureau voor Schimmelcultures, Utrecht

  • Crous PW, Slippers B, Wingfield MJ, Rheeder J, Marasas WFO, Philips AJL, Alves A, Burgess TI, Barber PA, Groenewald JZ (2006) Phylogenetic lineages in the Botryosphaeriaceae. Stud Mycol 55:235–253

    Article  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Braun U, Groenewald JZ (2007) Mycosphaerella is polyphyletic. Stud Mycol 58:1–3

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Schoch CL, Hyde KD, Wood AR, Gueidan C, de Hoog GS, Groenewald JZ (2009) Phylogenetic lineages in the Capnodiales. Stud Mycol 64:17–47

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Summerell BA, Shivas RG, Romberg M, Mel’nik VA, Verkley GJM, Groenewald JZ (2011) Fungal planet description sheets: 92–106. Persoonia 27:130–162

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Quaedvlieg W, Sarpkaya K, Can C, Erkılıç A (2013a) Septoria-like pathogens causing leaf and fruit spot of pistachio. IMA Fungus 4:187–199

    Article  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Braun U, Hunter GC, Wingfield MJ, Verkley GJ, Shin HD, Nakashima C, Groenewald JZ (2013b) Phylogenetic lineages in Pseudocercospora. Stud Mycol 75:37–114

    Article  CAS  PubMed  Google Scholar 

  • Crous PW, Wingfield MJ, Schumacher RK, Summerell BA, Giraldo A, Gené J, Guarro J, Wanasinghe DN, Hyde KD, Camporesi E, Garethjones EB (2014) Fungal planet description sheets: 281–319. Persoonia 33:212–289

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Wingfield MJ, Guarro J, Hernández-Restrepo M, Sutton DA, Acharya K, Barber PA, Boekhout T, Dimitrov RA, Dueñas M, Dutta AK (2015a) Fungal planet description sheets: 320–370. Persoonia 34:167–266

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Carris LM, Giraldo A, Groenewald JZ, Hawksworth DL, Hernández-Restrepo M, Jaklitsch WM, Lebrun M-H, Schumacher RK, Stielow JB (2015b) The genera of fungi-fixing the application of the type species of generic names-G 2: Allantophomopsis, Latorua, Macrodiplodiopsis, Macrohilum, Milospium, Protostegia, Pyricularia, Robillarda, Rotula, Septoriella, Torula, and Wojnowicia. IMA Fungus 6:163–198

    Article  PubMed  PubMed Central  Google Scholar 

  • Dai DQ, Phookamsak R, Wijayawardene NN, Li WJ, Bhat DJ, Xu JC, Taylor JE, Hyde KD, Chukeatirote E (2017) Bambusicolous fungi. Fungal Divers 82:1–105

    Article  Google Scholar 

  • Dai YC (2012) Polypore diversity in China with an annotated checklist of Chinese polypores. Mycoscience 53:49–80

    Article  Google Scholar 

  • Dai YC, Yang ZL, Cui BK, Yu CJ, Zhou LW (2009) Species diversity and utilization of medicinal mushrooms and fungi in China (review). Int J Med Mushrooms 11:287–302

    Article  Google Scholar 

  • Dai YC, Xue HJ, Vlasák J, Rajchenberg M, Wang B, Zhou LW (2014) Phylogeny and global diversity of Polyporus group Melanopus (Polyporales, Basidiomycota). Fungal Diver 64:133–144

    Article  Google Scholar 

  • Damm U, Woudenberg JHC, Cannon PF, Crous PW (2009) Colletotrichum species with curved conidia from herbaceous hosts. Fungal Divers 39:45–87

    Google Scholar 

  • Daranagama DA, Camporesi E, Tian Q, Liu X, Chamyuang S, Stadler M, Hyde KD (2015) Anthostomella is polyphyletic comprising several genera in Xylariaceae. Fungal Divers 73:203–238

    Article  Google Scholar 

  • Daranagama DA, Jones EBG, Liu XZ, To-anun C, Stadler M, Hyde KD (2016) Mycosphere Essays 13—do xylariaceous macromycetes make up most of the Xylariomycetidae? Mycosphere 7:582–601

    Google Scholar 

  • Das K, Dentinger BTM (2015) Austroboletus olivaceoglutinosus, a new mushroom species from Sikkim, India with a distinctive green, glutinous pileus. Kew Bull 70:15

    Article  Google Scholar 

  • Das K, Hembrom ME, Parihar A, Mishra D, Sharma JR (2014) Strobilomyces polypyramis—rediscovery of a wild mushroom from Sikkim, India. Indian J Plant Sci 3(2):13–18

    Google Scholar 

  • De Gruyter J, Noordeloos ME (1992) Contributions towards a monograph of Phoma (Coelomycetes)-I. 1. Section Phoma: taxa with very small conidia in vitro. Persoonia 15:71–92

    Google Scholar 

  • De Gruyter J, Noordeloos ME, Boerema GH (1998) Contributions towards a monograph of Phoma (Coelomycetes)—I. 3. Section Phoma: taxa with conidia longer than 7 μm. Persoonia 16:471–490

    Google Scholar 

  • De Gruyter J, Aveskamp MM, Woudenberg JHC, Verkley GJM, Groenewald JZ, Crous PW (2009) Molecular phylogeny of Phoma and allied anamorph genera: towards a reclassification of the Phoma complex. Mycol Res 113:508–519

    Article  PubMed  CAS  Google Scholar 

  • De Gruyter J, Woudenberg JHC, Aveskamp MM, Verkley GJM, Groenewald JZ, Crous PW (2010) Systematic reappraisal of species in Phoma section Paraphoma, Pyrenochaeta and Pleurophoma. Mycologia 102:1066–1081

    Article  PubMed  Google Scholar 

  • De Gruyter J, Woudenberg JHC, Aveskamp MM, Verkley GJM, Groenewald JZ, Crous PW (2013) Redisposition of phoma-like anamorphs in Pleosporales. Stud Mycol 75:1–36

    Article  PubMed  Google Scholar 

  • de Hoog GS, Hermanides-Nijhof EJ (1977) The black yeasts and allied hyphomycetes. Mycologia 69:1242–1244

    Google Scholar 

  • de Hoog GS, Vicente VA, Najafzadeh MJ, Harrak MJ, Badali H, Seyedmousavi S (2011) Waterborne Exophiala species causing disease in coldblooded animals. Persoonia 27:46–72

    Article  PubMed  PubMed Central  Google Scholar 

  • De Notaris G (1844) Cenno sulla tribu dei pirenomiceti sferiacei e descrizione di alcuni nuovi generi. Giornale Botanico Italiano 1:322–335

    Google Scholar 

  • de Souza CAF, Lima DX, Gurgel LMS, Santiago ALCM (2016) Coprophilous Mucorales (ex Zygomycota) from three areas in the semi-arid of Pernambuco. Brazil. Braz J Microbiol 48(1):1–8

    Google Scholar 

  • Dennis RWG (1951) Some tropical American Agaricaceae referred by Berkeley and Montagne to Marasmius, Collybia or Heliomyces. Kew Bull 6(3):387–410

    Article  Google Scholar 

  • Desjardin DE (1989) The Genus Marasmius from the southern Appalachian Mountains. Doctoral dissertations, University of Tennessee, Knoxville

  • Desjardin DE, Retnowati A, Horak E (2000) Agaricales of Indonesia: 2. A preliminary monograph of Marasmius from Java and Bali. Sydowia 52:92–193

    Google Scholar 

  • Desjardin DE, Wood MG, Stevens FA (2015) California mushrooms. Timber Press, Portland, Oregon

    Google Scholar 

  • Diedicke (1912) Kryptogamen-Flora der Mark Brandenburg 9(5):206

  • Dissanayake AJ, Camporesi E, Hyde KD, Phillips AJL, Fu CY, Yan JY, Li XH (2016) Dothiorella species associated with woody hosts in Italy. Mycosphere 7:51–63

    Google Scholar 

  • Dissing H (1966) genus Helvella in Europe with special emphasis on the species found in Norden. Dansk Botanisk Arkiv. 25(1):1–172

    Google Scholar 

  • Dissing H (1979) Helvella papuensis, a new species from Papua New Guinea. Sydowia Annales Mycologici, Beihefte 8:156–161

    Google Scholar 

  • Doilom M, Shuttleworth L, Roux J, Chukeatirote E, Hyde KD (2014) Barriopsis tectonae sp. nov. a new species of Botryosphaeriaceae from Tectona grandis (teak) in Thailand. Phytotaxa 176:081–091

    Article  Google Scholar 

  • Doilom M, Dissanayake AJ, Wanasinghe DN, Boonmee S, Liu JK, Bhat DJ, Taylor JE, Bahkali AH, McKenzie EHC, Hyde KD (2017) Microfungi on Tectona grandis (teak) in Northern Thailand. Fungal Divers 82:107–182

    Article  Google Scholar 

  • Donk MA (1949) New and revised nomina generica conservanda proposed for Basidiomycetes (Fungi). Bull Jard Bot 18:83–168

    Google Scholar 

  • Donk MA (1964) A conspectus of the families of Aphyllophorales. Persoonia Mol Phylogeny Evol Fungi 3(2):199–324

    Google Scholar 

  • Doveri F (2004) Fungi fimicoli italici. A.M.B., Vicenza

    Google Scholar 

  • Dudka IO, Heluta VP, Tykhonenko YY, Andrianova TV, Hayova VP, Prydiuk MP, Dzhagan VV, Isikov VP (2004) Fungi of the Crimean peninsula. Institute of Botany, National Academy of Sciences of Ukraine, Ukraine

    Google Scholar 

  • Ehrenberg CG (1818) Sylvae mycologicae Berolinenses. Bruschke, Berlin, pp 1–32

  • Ellis JP (1980) The genus Morenoina in Britain. Trans Br Mycol Soc 74:297–307

    Article  Google Scholar 

  • Ellis MB (1971) Dematiaceous Hyphomycetes. Commonwealth Mycological lnstitute, Kew, Surrey

    Google Scholar 

  • Ellis MB (1976) More dematiaceous Hyphomycetes. Commonwealth Mycological Institute, Kew, Surrey

    Google Scholar 

  • Ellis MB, Ellis JP (1990) Fungi without gills (Hymenomycetes and Gasteromycetes): an identification handbook. Springer, Berlin

    Google Scholar 

  • Ellis NB, Ellis JP (1985) Microfungi on land plants—an identification handbook. Macmillan Publishing, New York

    Google Scholar 

  • Erikss OE (1967) Arkiv før Botanik 6(4–5):405

  • Eriksson OE, Winka K (1998) Families and higher taxa of Ascomycota. Myconet 1(2):17–24

    Google Scholar 

  • Ertz D, Heuchert B, Braun U, Freebury CE, Common RS, Diederich P (2016) Contribution to the phylogeny and taxonomy of the genus Taeniolella, with a focus on lichenicolous taxa. Fungal Biol 120:1416–1447

    Article  PubMed  Google Scholar 

  • Estades A, Lannoy G (2004) Les bolets européens. Bull Mycol Bot Dauphiné-Savoie 44(3):3–79

    Google Scholar 

  • Farr DF, Rossman AY (2012) Fungal databases, systematic mycology and microbiology laboratory, ARS, USDA. https://nt.ars-grin.gov/fungaldatabases/. Retrieved 24 Nov 2016

  • Farr DF, Aime MC, Rossman AY, Palm ME (2006) Species of Colletotrichum on Agavaceae. Mycol Res 110:1395–1408

    Article  CAS  PubMed  Google Scholar 

  • Ferrari BC, Zhang C, van Dorst J (2011) Recovering greater fungal diversity from pristine and diesel fuel contaminated sub-Antarctic soil through cultivation using both a high and a low nutrient media approach. Front Microbiol 2:217

    Article  PubMed  PubMed Central  Google Scholar 

  • Fischer E (1897) Plectacineae. In: Engler A, Prantl K (eds) Die natürlichen Pflanzenfamilien, vol I. Engelmann, Leipzig

    Google Scholar 

  • Fotouhifar KB, Hedjaroude GA, Leuchtmann A (2010) ITS rDNA phylogeny of Iranian strains of Cytospora and associated teleomorphs. Mycologia 102:1369–1382

    Article  PubMed  Google Scholar 

  • Frank JL (2015) Nomenclatural novelties. Index Fungorum 248:1

    Google Scholar 

  • Fries EM (1821) Systema mycologicum, vol. 1. Ex Officina Berlingiana, Lund & Greifswald

  • Fries EM (1849) Summa vegetabilium scandinaviae. Part 2. Bonnier, Leipzig

  • Frisvad JC, Samson RA (2004) Polyphasic taxonomy of Penicillium subgenus Penicillium. A guide to identification of food and air-borne terverticillate Penicillia and their mycotoxins. Stud Mycol 49:1–174

    Google Scholar 

  • Fuckel L (1870) Symbolae mycologicae. Beiträge zur Kenntniss der Rheinischen Pilze. Jb nassau Ver Naturk 23–24:212

  • Fukami T, Dickie IA, Wilkie JP, Paulus BC, Park D, Roberts A, Buchanan PK, Allen RB (2010) Assembly history dictates ecosystem functioning: evidence from wood decomposer communities. Ecol Lett 13:675–684

    Article  PubMed  Google Scholar 

  • Geiser DM, Gueidan C, Miadlikowska J, Lutzoni F, Kauff F, Hofstetter V, Fraker E, Schoch CL, Tibell L, Untereiner WA, Aptroot A (2006) Eurotiomycetes: Eurotiomycetidae and Chaetothyriomycetidae. Mycologia 98:1053–1064

    Article  PubMed  Google Scholar 

  • Gelardi M, Vizzini A, Ercole E, Voyron S, Wu G, Liu XZ (2012) Strobilomyces echinocephalus sp. nov. (Boletales) from south-western China, and a key to the genus Strobilomyces worldwide. Mycol Prog 12:575–588

    Article  Google Scholar 

  • Giambra S, Piazza G, Alves A, Mondello V, Berbegal M, Armengol J, Burruano S (2016) Botryosphaeriaceae species associated with diseased loquat trees in Italy and description of Diplodia rosacearum sp. nov. Mycosphere 7:978–989

    Google Scholar 

  • Gilbertson RL, Ryvarden L (1986) North American polypores. Abortiporus-Lindtneria. Fungiflora, Oslo

    Google Scholar 

  • Gilbertson RL, Ryvarden L (1987) North American polypores: Megasporoporia-Wrightoporia. Fungiflora, Oslo

  • Gilliam MS (1976) The genus Marasmius in the Northeastern United States and adjacent Canada. Mycotaxon 4:1–144

    Google Scholar 

  • Glass NL, Donaldson GC (1995) Development of primer sets designed for use with the PCR to amplify conserved genes from filamentous ascomycetes. Appl Environ Microbiol 61:1323–1330

    CAS  PubMed  PubMed Central  Google Scholar 

  • Góes-Neto A, Loguercio-Leite C, Guerrero RT (2005) DNA extraction from frozen field collected and dehydrated herbarium fungal basidiomata: performance of SDS and CTAB-based methods. Biotemas 18:19–32

    Google Scholar 

  • Haase G, Sonntag L, Melzer-Krick B, de Hoog GS (1999) Phylogenetic inference by SSU-gene analysis of members of the Herpotrichiellaceae with special reference to human pathogenic species. Stud Mycol 43:80–97

    Google Scholar 

  • Häffner J, Stangl J, Sedlmeier A, Geh G, Krieglsteiner GJ (1987) Di Gattung Helvella: morphologie und taxonomie. Deutsche Gesellschaft fur Mycologie

  • Halama M (2016) Rubroboletus le-galiae (Boletales, Basidiomycota), a species new for Poland. Acta Mycol 50(2):1066

    Article  Google Scholar 

  • Hall TA (1999) BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl Acid Symp Ser 41:95–98

    CAS  Google Scholar 

  • Halling RE, Osmundson TW, Neves MA (2006) Austroboletus mutabilis sp. nov. from northern Queensland. Muelleria 24:31–36

    Google Scholar 

  • Hawksworth DL, Sutton BC, Ainsworth GC (1983) Ainsworth and Bisby’s dictionary of the fungi, 7th edn. Commonwealth Mycological Institute, Kew

    Google Scholar 

  • Hawksworth DL, Kirk PM, Sutton BC, Pegler DN (1995) Ainsworth & Bisby’s dictionary of the fungi, 8th edn. CAB International, Wallingford

    Google Scholar 

  • Helaly SE, Richter C, Thongbai B, Hyde KD, Stadler M (2016) Lentinulactam, a hirsutane sesquiterpene with an unprecedented lactam modification. Tetrahedron Lett 57(52):5911–5913

    Article  CAS  Google Scholar 

  • Henkel TW, Meszaros R, Aime MC, Kennedy A (2005) New Clavulina species from the Pakaraima Mountains of Guyana. Mycol Prog 4:343–350

    Article  Google Scholar 

  • Hennings P (1895) Fungi camerunenses I. Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie 22:72–111

    Google Scholar 

  • Hennings P (1905) Fungi japonici VI. Bot Jahrb Syst 37:156–166

    Google Scholar 

  • Hesseltine CW, Ellis JJ (1961) Notes on Mucorales, especially Absidia. Mycologia 53:406–426

    Article  Google Scholar 

  • Hesseltine CW, Ellis JJ (1964) The genus Absidia: Gongronella and cylindrical-spored species of Absidia. Mycologia 56:568–601

    Article  Google Scholar 

  • Hirayama K, Tanaka K (2011) Taxonomic revision of Lophiostoma and Lophiotrema based on reevaluation of morphological characters and molecular analyses. Mycoscience 52:401–412

    Article  Google Scholar 

  • Hironaga M, Watanabe S, Nishimura K, Miyaji M (1981) Annellated conidiogenous cells in Exophiala dermatitidis, agent of phaeohyphomycosis. Mycologia 73:1181–1183

    Article  Google Scholar 

  • Hofmann TA, Kirschner R, Piepenbring M (2010) Phylogenetic relationships and new records of Asterinaceae (Dothideomycetes) from Panama. Fungal Divers 43(1):39–53

    Article  Google Scholar 

  • Hoffmann K, Pawlowska J, Walther G, Wrzosek M, de Hoog GS, Benny GL, Kirk PM, Voigt K (2013) The family structure of the Mucorales: a synoptic revision based on comprehensive multigene-genealogies. Persoonia 30:57–76

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Högberg N, Holdenrieder O, Stenlid J (1999) Population structure of the wood decay fungus Fomitopsispinicola. Heredity 83:354–360

    Article  PubMed  Google Scholar 

  • Höhnel FXR (1919) Fragmente zur Mykologie (XXIII. Mitteilung, Nr. 1154 bis 1188). Sitzungsber Akad Wiss Wien Math Naturwiss Kl Abt 1 128:535–625

  • Holm L (1957) Nomenclatural notes on Pyrenomycetes. Taxon 24:475–488

    Article  Google Scholar 

  • Holm L (1961) Taxonomical notes on Ascomycetes. IV. Notes of Nodulosphaeria Rbh. Sven Bot Tidskr 55:63–80

    Google Scholar 

  • Holubová-Jechová V (1987) Studies on Hyphomycetes from Cuba V. Six new species of Dematiaceous Hyphomycetes from Havana Province. Ceska Mykologie 41:29–36

    Google Scholar 

  • Hongsanan S, Li YM, Liu JK, Hofmann T, Piepenbring M, Bhat JD, Boonmee S, Doilom M, Singtripop C, Tian Q, Mapook A, Zeng XY, Bahkali AH, Xu JC, Mortimer PE, Wu XH, Yang JB, Hyde KD (2014) Revision of genera in Asterinales. Fungal Divers 68:1–68

    Article  Google Scholar 

  • Hopple JS, Vilgalys R (1994) Phylogenetic relationships among coprinoid taxa and allies based on data from restriction site mapping of nuclear rDNA. Mycologia 86:96–107

    Article  CAS  Google Scholar 

  • Hopple JS, Vilgalys R (1999) Phylogenetic relationships in the mushroom genus Coprinus and dark-spored allies based on sequence data from the nuclear gene coding for the large ibosomal subunit RNA: divergent domains, outgroups, and monophyly. Mol Phylogenet Evol 13:1–19

    Article  CAS  PubMed  Google Scholar 

  • Horak E (1980a) Indian Boletales and Agaricales, revisions and new taxa. Sydowia 33:80–110

    Google Scholar 

  • Horak E (1980b) Inocybe (Agaricales) in Indomalaya and Australasia. Persoonia Mol Phylogeny Evol Fungi 11:1–37

    Google Scholar 

  • Horak E (1980c) Supplementary remarks to Austroboletus (Corner) Wolfe (Boletaceae). Sydowia 33:71–87

    Google Scholar 

  • Houbraken J, Samson RA (2011) Phylogeny of Penicillium and the segregation of Trichocomaceae into three families. Stud Mycol 70:1–51

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Houbraken J, Wang L, Lee HB, Frisvad JC (2016) New sections in Penicillium containing novel species producing patulin, pyripyropens or other bioactive compounds. Persoonia 36:299–314

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Hu H, Jeewon R, Zhou D, Zhou T, Hyde KD (2007) Phylogenetic diversity of endophytic Pestalotiopsis species in Pinus armandii and Ribes spp.: evidence from rDNA and β-tubulin gene phylogenies. Fungal Divers 24:1–22

    CAS  Google Scholar 

  • Hughes SJ (1958) Revisiones hyphomycetum aliquot cum appendice de nominibus rejiciendis. Can J Bot 36:727–836

    Article  Google Scholar 

  • Hughes SJ (1976) Sooty moulds. Mycologia 68:693–820

    Article  Google Scholar 

  • Humber RA, Rocha LF, Inglis PW, Kipnis A, Luz C (2013) Morphology and molecular taxonomy of Evlachovaea like fungi and the status of this unusual conidial genus. Fungal Biol 117:1–12

    Article  PubMed  Google Scholar 

  • Hüseyin E, Selçuk F, Churakov BP (2014) A new species of Berkleasmium from Ulyanovsk, Russia. Mycosphere 5:462–466

    Google Scholar 

  • Hyde KD (1995) Tropical Australasian fungi. IX. Vaginatispora aquatica gen. et sp. nov. Nova Hedwigia 61:233–241

    Google Scholar 

  • Hyde KD, Vrijmoed LLP, Chinnaraj S, Jones EBG (1992) Massarina armatispora sp. nov., a new intertidal ascomycete from mangroves. Bot Mar 35:325–328

  • Hyde KD, Cai L, McKenzie EHC, Yang YL, Zhang JZ, Prihastuti H (2009) Colletotrichum: a catalogue of confusion. Fungal Divers 39:1–17

    Google Scholar 

  • Hyde KD, McKenzie EHC, KoKo TW (2011) Towards incorporating anamorphic fungi in a natural classification—checklist and notes for 2010. Mycosphere 2:1–88

    Google Scholar 

  • Hyde KD, Jones EBG, Liu JK, Ariyawansa H, Boehm E, Boonmee S, Braun U, Chomnunti P, Crous PW, Dai DQ, Diederich P, Dissanayake A, Doilom M, Doveri F, Hongsanan S, Jayawardena R, Lawrey JD, Li YM, Liu YX, Lücking R, Monka J, Muggia L, Nelsen MP, Pang KL, Phookamsak R, Senanayake IC, Shearer CA, Suetrong S, Tanaka K, Thambugala KM, Wijayawardene NN, Wikee S, Wu HX, Zhang Y, Begoña AH, Alias SA, Aptroot A, Bahkali AH, Bezerra JL, Bhat DJ, Camporesi E, Chukea E, Gueidan C, Hawksworth DL, Hirayama K, Hoog SD, Kang JK, Knudsen K, Li WJ, Li XH, Liu ZY, Mapook A, Mckenzie EHC, Miller AN, Mortimer PE, Phillips AJL, Raja HA, Scheuer C, Schumm F, Taylor JE, Tian Q, Tibpromma S, Wanasinghe DN, Wang Y, Xu JC, Yacharoen S, Yan JY, Zang M (2013) Families of dothideomycetes. Fungal Divers 63:1–313

    Article  Google Scholar 

  • Hyde KD, Nilsson RH, Alias SA, Ariyawansa HA, Blair JE, Cai L, de Cock AWAM, Dissanayake AJ, Glockling SL, Goonasekara ID, Gorczak M, Hahn M, Jayawardena RS, van Kan JAL, Laurence MH, Lévesque CA, Li XH, Liu JK, Maharachchikumbura SSN, Manamgoda DS, Martin FN, McKenzie EHC, McTaggart AR, Mortimer PE, Nair PVR, Pawłowska J, Rintoul TL, Shivas RG, Spies CFJ, Summerell BA, Taylor PWJ, Terhem RB, Udayanga D, Vaghefi N, Walther G, Wilk M, Wrzosek M, Xu JC, Yan JY, Zhou N (2014) One stop shop: backbones trees for important phytopathogenic genera: I. Fungal Divers 67:21–125

    Article  Google Scholar 

  • Hyde KD, Hongsanan S, Jeewon R, Bhat DJ, McKenzie EHC, Jones EBG, Phookamsak R, Ariyawansa HA, Boonmee S, Zhao Q, Abdel-Aziz FA, Abdel-Wahab MA, Banmai S, Chomnunti P, Cui BK, Daranagama DA, Das K, Dayarathne MC, de Silva NI, Dissanayake AJ, Doilom M, Ekanayaka AH, Gibertoni TB, Góes-Neto A, Huang SK, Jayasiri SC, Jayawardena RS, Konta S, Lee HB, Li WJ, Lin CG, Liu JK, Lu YZ, Luo ZL, Manawasinghe IS, Manimohan P, Mapook A, Niskanen T, Norphanphoun C, Papizadeh M, Perera RH, Phukhamsakda C, Richter C, de Santiago ALCMA, Drechsler-Santos ER, Senanayake IC, Tanaka K, Tennakoon TMDS, Thambugala KM, Tian Q, Tibpromma S, Thongbai B, Vizzini A, Wanasinghe DN, Wijayawardene NN, Wu HX, Yang J, Zeng XY, Zhang H, Zhang JF, Bulgakov TS, Camporesi E, Bahkali AH, Amoozegar AM, Araujo-Neta LS, Ammirati JF, Baghela A, Bhatt RP, Bojantchev S, Buyck B, da Silva GA, de Lima CLF, de Oliveira RJV, de Souza CAF, Dai YC, Dima B, Duong TT, Ercole E, Mafalda-Freire F, Ghosh A, Hashimoto A, Kamolhan S, Kang JC, Karunarathna SC, Kirk PM, Kytövuori I, Lantieri A, Liimatainen K, Liu ZY, Liu XZ, Lücking R, Medardi G, Mortimer PE, Nguyen TTT, Promputtha I, Raj KNA, Reck MA, Lumyong S, Shahzadeh-Fazeli SA, Stadler M, Soudi MR, Su HY, Takahashi T, Tangthirasunun N, Uniyal P, Wang Y, Wen TC, Xu JC, Zhang ZK, Zhao YC, Zhou JZ, Zhu L (2016) Fungal diversity notes 367–490: taxonomic and phylogenetic contributions to fungal taxa. Fungal Divers 80:1–270

    Article  Google Scholar 

  • Imler L (1950) Recherches sur les bolets. Bull. Soc. Mycol. Fr. 66(4):177–203

    Google Scholar 

  • Index Fungorum (2017) http://www.indexfungorum.org/Names/Names.asp

  • Isola D, Selbmann L, de Hoog GS, Fenice M, Onofri S, Prenafeta- Bold FX, Zucconi L (2013) Isolation and screening of black fungi as degraders of volatile aromatic hydrocarbons. Mycopathologia 175:369–379

    Article  PubMed  Google Scholar 

  • Iznova T, Rukseniene J (2012) Ascomycetes species new to Lithuania. Botanica Lithuanica 18:35–39

    Article  Google Scholar 

  • Jaklitsch WM, Voglmayr H (2016) Hidden diversity in Thyridaria and a new circumscription of the Thyridariaceae. Stud Mycol 85:35–64

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jayasiri SC, Hyde KD, Abd-Elsalam KA, Abdel-Wahab MA, Ariyawansa HA, Bhat J, Buyck B, Dai YC, Ertz D, Hidayat I, Jeewon R, Jones EBG, Karunarathna SC, Kirk P, Lei C, Liu JK, Maharachchikumbura SSN, McKenzie E, Ghobad-Nejhad M, Nilsson H, Pang KL, Phookamsak R, Rollins AW, Romero AI, Stephenson S, Suetrong S, Tsui CKM, Vizzini A, Wen TC, De Silva NI, Promputtha I, Kang JC (2015) The Facesoffungi database: fungal names linked with morphology, molecular and human attributes. Fungal Divers 74:3–18

    Article  Google Scholar 

  • Jayawardena RS, Hyde KD, Damm U, Cai L, Liu M, Li XH, Zhang W, Zhao WS, Yan JY (2016a) Notes on currently accepted species of Colletotrichum. Mycosphere 7:1192–1260

    Google Scholar 

  • Jayawardena RS, Hyde KD, Jeewon R, Li XH, Liu M, Yan JY (2016b) Mycosphere essay 6: why is it important to correctly name Colletotrichum species? Mycosphere 7:1076–1092

    Google Scholar 

  • Jeewon R, Hyde KD (2016) Establishing species boundaries and new taxa among fungi: recommendations to resolve taxonomic ambiguities. Mycosphere 7:1669–1677

    Google Scholar 

  • Jeewon R, Liew ECY, Hyde KD (2002) Phylogenetic relationships of Pestalotiopsis and allied genera inferred from ribosomal DNA sequences and morphological characters. Mol Phylogenet Evol 25:378–392

    Article  CAS  PubMed  Google Scholar 

  • Jeewon R, Liew ECY, Hyde KD (2003a) Molecular systematics of the Amphisphaeriaceae based on cladistic analyses of partial LSU rDNA gene sequences. Mycol Res 107(12):1392–1402

    Article  CAS  PubMed  Google Scholar 

  • Jeewon R, Liew EC, Simpson JA, Hodgkiss IJ, Hyde KD (2003b) Phylogenetic significance of morphological characters in the taxonomy of Pestalotiopsis species. Mol Phylogenet Evol 27(3):372–383

    Article  CAS  PubMed  Google Scholar 

  • Jeewon R, Liew ECY, Hyde KD (2004) Phylogenetic evaluation of species nomenclature of Pestalotiopsis in relation to host association. Fungal Divers 17:39–55

    Google Scholar 

  • Jeewon R, Ittoo J, Mahadeb D, Jaufeerally-Fakim Y, Wang HK, Liu AR (2013) DNA based identification and phylogenetic characterisation of endophytic and saprobic Fungi from Antidesma madagascariense, a medicinal plant in mauritius. J Mycol. doi:10.1155/2013/781914

    Google Scholar 

  • Jian-Zhe Y (1985) Notes on the genus Austroboletus in China. Agarica 6(12):80–89

    Google Scholar 

  • Jiea CY, Zhoua QX, Zhao WS, Jiang YL, Hyde KD, Mckenzie EHC, Wang Y (2013) A new Myrmecridium species from Guizhou, China. Mycotaxon 124:1–8

    Article  Google Scholar 

  • Jones EBG, Suetrong S, Sakayaroj J, Bahkali AH, Abdel-Wahab MA, Boekhout T, Pang KL (2015) Classification of marine Ascomycota, Basidiomycota, Blastocladiomycota and Chytridiomycota. Fungal Divers 73:1–72

    Article  Google Scholar 

  • Julou T, Burghardt B, Gebauer G, Bervellier D, Damesin C, Selosse MA (2005) Mixotrophy in orchids: insights froma comparative study of green individuals and nonphotosynthetic individuals of Cephalanthera damasonium. New Phytol 166:639–653

    Article  CAS  PubMed  Google Scholar 

  • Kalb K, Buaruang K, Mongkolsuk P, Boonpragob K (2012) New or otherwise interesting lichens. VI, including a lichenicolous fungus. Phytotaxa 42:35–47

    Article  Google Scholar 

  • Karsten PA (1873) Mycologia fennica. Pars secunda. Pyrenomycetes. Bidrag till Kännedom av Finlands Natur och Folk 23:1–252

    Google Scholar 

  • Karunarathna SC, Yang ZL, Zhao RL, Vellinga EC, Bahkali AH, Chukeatirote E, Hyde KD (2011) Three new species of Lentinus from northern Thailand. Mycol Prog 10:389–398

    Article  Google Scholar 

  • Katoh K, Misawa K, Kuma K, Miyata T (2002) MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. Nucleic Acids Res 30:3059–3066

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kennedy LL (1958) The genera of the Dacrymycetaceae. Mycologia 50:874–895

    Article  Google Scholar 

  • Kepler R, Ban S, Nakagiri A, Bischoff J, Hywel-Jones N, Owensby CA, Spatafora JW (2013) The phylogenetic placement of hypocrealean insect pathogens in the genus Polycephalomyces: an application of One Fungus One Name. Fungal Biol 117:611–622

    Article  PubMed  Google Scholar 

  • Kimura M (1980) A simple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 16:111–120

    Article  CAS  PubMed  Google Scholar 

  • Kirk PM, Cannon PF, David JC, Stalpers JA (2001) Ainsworth and Bisby’s dictionary of the fungi, 8th edn. CABI Publishing, London

    Google Scholar 

  • Kirk PM, Cannon PF, Minter DW, Stalpers JA (2008) Ainsworth & Bisby’s dictionary of the fungi, 10th edn. CABI, Wallingford

    Google Scholar 

  • Kiyashko AA (2012) Boletus rubrosanguineus (Walty) ex Cheype, 1983//Red Data Book of Republic of Adygheya. Rare and threatened representatives of the regional fauna and flora. Maykop (in Russian)

  • Knudsen H, Vesterholt J (2012) Funga nordica. Nordsvamp, Copenhagen

    Google Scholar 

  • Kobayashi T (2002) The Taxonomic studies of the genus Inocybe. Beih Nova Hedwigia 124:1–246

    Google Scholar 

  • Kodsueb R, Dhanasekaran V, Aptroot A, Lumyong S, McKenzie EH, Hyde KD, Jeewon R (2006) The family Pleosporaceae: intergeneric relationships and phylogenetic perspectives based on sequence analyses of partial 28S rDNA. Mycologia 98:571–583

    Article  CAS  PubMed  Google Scholar 

  • Konta S, Phillips AJL, Bahkali AH, Jones EBG, Eungwanichayapant DP, Hyde KD, Boonmee S (2016a) Botryosphaeriaceae from palms in Thailand—Barriopsis archontophoenicis sp. nov, from Archontophoenix alexandrae. Mycosphere 7:921–932

    Google Scholar 

  • Konta S, Hongsanan S, Phillips AJ, Jones EBG, Boonmee S, Hyde KD (2016b) Botryosphaeriaceae from palms in Thailand II-two new species of Neodeightonia, N. rattanica and N. rattanicola from Calamus (rattan palm). Mycosphere 7:950–961

    Google Scholar 

  • Kropp BR, Matheny PB, Hutchison LJ (2013) Inocybe section Rimosae in Utah: phylogenetic affinities and new species. Mycologia 105:728–747

    Article  PubMed  Google Scholar 

  • Krüger D, Petersen RH, Hughes KW (2006) Molecular phylogenies and mating study data in Polyporus with special emphasis on group “Melanopus” (Basidiomycota). Mycol Prog 5:185–206

    Article  Google Scholar 

  • Kunze G, Schmidt JC (1817) Mykologische Hefte 1:1–109

  • Kuo M, Methven AS (2014) Mushrooms of the Midwest. University of Illinois Press, Urbana

    Google Scholar 

  • Lakhanpal TN (1996) Mushrooms of India: Boletaceae, vol I. APH Publishing Corporation, New Delhi

    Google Scholar 

  • Lannoy G, Estades A (2001) Les Bolets. Flore Mycologique d’Europe 6. CRDP, Amiens

  • Largent DL (1974) Rhodophylloid fungi of the Pacific coast (United States) IV: infrageneric concepts in Entoloma, Nolanea, and Leptonia. Mycologia 66:987–1021

    Article  Google Scholar 

  • Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R, Thompson JD, Gibson TJ, Higgins DG (2007) Clustal W and Clustal X version 2.0. Bioinformatics 23:2947–2948

    Article  CAS  PubMed  Google Scholar 

  • Larsson E, Larsson KH (2003) Phylogenetic relationships of russuloid basidiomycetes with emphasis on aphyllophoralean taxa. Mycologia 95:1037–1065

    Article  CAS  PubMed  Google Scholar 

  • Larsson E, Örstadius L (2008) Fourteen coprophilous species of Psathyrella identified in the Nordic countries using morphology and nuclear rDNA sequence data. Mycol Res 112:1165–1185

    Article  CAS  PubMed  Google Scholar 

  • Larsson E, Ryberg M, Moreau PA, Mathiesen AD, Jacobsson S (2009) Taxonomy and evolutionary relationships within species of section Rimosae (Inocybe) based on ITS, LSU and mtSSU sequence data. Persoonia 23:86–98

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Leão-Ferreira SM, Gusmão LFP, Castañeda Ruiz RF (2013) Conidial fungi from the semi-arid Caatinga biome of Brazil. Three new species and new records. Nova Hedwigia 96:479–494

    Article  Google Scholar 

  • Lee S, Crous PW, Wingfield MJ (2006) Pestalotioid fungi from Pestiona in the Cape Floral Kingdom. Stud Mycol 55:175–187

    Article  PubMed  PubMed Central  Google Scholar 

  • Li DM, de Hoog GS, Lindhardt Saunte DM, Gerrits van den Ende AHG, Chen XR (2008) Coniosporium epidermidis sp. nov., a new species from human skin. Stud Mycol 61:131–136

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Li DM, Li RY, Hoog GD, Wang YX, Wang DL (2009) Exophiala asiatica, a new species from a fatal case in China. Med Mycol 47(1):101–109

    Article  CAS  PubMed  Google Scholar 

  • Li GJ, Li SF, Wen HA (2010) The Russula species resource and its economic values of China. Acta Edulis Fungi 17(sppl):155–160

  • Li GJ, Zhao D, Li SF, Yang HJ, Liu XZ (2013a) Russula changbaiensis sp. nov. from northeast China. Mycotaxon 124(1):269–278

    Article  Google Scholar 

  • Li HJ, Han ML, Cui BK (2013b) Two new Fomitopsis species from southern China based on morphological and molecular characters. Mycol Prog 12:709–718

    Article  Google Scholar 

  • Li GJ, Hyde KD, Zhao RN, Hongsanan S, Abdel-Aziz FA, Abdel-Wahab MA, Alvarado P, Alves-Silva G, Ammirati JF, Ariyawansa HA, Baghela A, Bahkali AH, Beug M, Bhat DJ, Bojantchev D, Boonpratuang T, Bulgakov TS, Camporesi E, Boro MC, Ceska O, Chakraborty D, Chen JJ, Chethana KWT, Chomnunti P, Consiglio G, Cui BK, Dai DQ, Dai YC, Daranagama DA, Das K, Dayarathne MC, Crop ED, De Oliveira RJV, de Souza CAF, de Souza JI, Dentinger BTM, Dissanayake AJ, Doilom M, Drechsler-Santos ER, Ghobad-Nejhad M, Gilmore SP, Góes-Neto A, Gorczak M, Haitjema GH, Hapuarachchi KK, Hashimoto A, He MQ, Henske JK, Hirayama K, Iribarren MJ, Jayasiri SC, Jayawardena RS, Jeon SJ, Jerónimo GH, Jesus AL, Jones EBG, Kang JC, Karunarathna SC, Kirk PM, Konta S, Kuhnert E, Langer E, Lee HS, Lee HB, Li WJ, Li XH, Liimatainen K, Lima DX, Lin CG, Liu JK, Liu XZ, Liu ZY, Luangsa-ard JJ, Lücking R, Lumbsch HT, Lumyong S, Leaño EM, Marano AV, Matsumura M, McKenzie EHC, Mongkolsamrit S, Mortimer PE, Nguyen TTT, Niskanen T, Norphanphoun C, O’Malley MA, Parnmen S, Pawłowska J, Perera RH, Phookamsak R, Phukhamsakda C, Pires-Zottarelli CLA, Raspé O, Reck MA, Rocha SCO, de Santiago ALCMA, Senanayake IC, Setti L, Shang QJ, Singh SK, Sir EB, Solomon KV, Song J, Srikitikulchai P, Stadler M, Suetrong S, Takahashi H, Takahashi T, Tanaka K, Tang LP, Thambugala KM, Thanakitpipattana D, Theodorou MK, Thongbai B, Thummarukcharoen T, Tian Q, Tibpromma S, Verbeken A, Vizzini A, Vlasák J, Voigt K, Wanasinghe DN, Wang Y, Weerakoon G, Wen HA, Wen TC, Wijayawardene NN, Wongkanoun S, Wrzosek M, Xiao YP, Xu JC, Yan JY, Yang J, Yang SD, Hu Y, Zhang JF, Zhao J, Zhou LW, Peršoh D, Phillips AJL, Maharachchikumbura SSN (2016) Fungal divers notes 253–366: taxonomic and phylogenetic contributions to fungal taxa. Fungal Divers 78:1–237

    Article  Google Scholar 

  • Lib Pl (1830) crypt. Arduenna (Liège), fasc. 1(Praef.):8

  • Lin CG, McKenzie EHC, Bhat DJ, Ran SF, Chen Y, Hyde KD, Li DW, Wang Y (2016) Stachybotrys-like taxa from karst areas and a checklist of stachybotrys-like species from Thailand. Mycosphere 7:1273–1291

    Google Scholar 

  • Linaldeddu BT, Deidda A, Scanu B, Franceschini A, Alves A, Abdollahzadeh J, Phillips AJL (2016a) Phylogeny, morphology and pathogenicity of Botryosphaeriaceae, Diatrypaceae and Gnomoniaceae associated with branch diseases of hazelnut in Sardinia (Italy). J Plant Pathol 146:259–279

    Article  Google Scholar 

  • Linaldeddu BT, Alves A, Phillips AJL (2016b) Sardiniella urbana gen. et sp. nov., a new member of the Botryosphaeriaceae isolated from declining Celtis australis trees in Sardinian streetscapes. Mycosphere 7:893–905

    Google Scholar 

  • Linaldeddu BT, Maddau L, Franceschini A, Alves A, Phillips AJL (2016c) Botryosphaeriaceae species associated with lentisk dieback in Italy and description of Diplodia insularis sp. nov. Mycosphere 7:962–977

    Google Scholar 

  • Lindau G (1896) Hysteriineae. In: Engler A, Prantl K (eds) Naturliche Pflanzenfamilien. I. Teil, I, vol 1. Abteilung, pp 265–278

  • Linnaeus CV (1753) Species plantarum, 2 vols. Laurentii Salvii, Holmiae

  • Liu B, Fan L, Tao K (1988) Five new species of Dacrymycetaceae from China. Acta Mycol Sin 7:1–6

    Google Scholar 

  • Liu JK, Phookamsak R, Jones EBG, Zhang Y, Ko-Ko TW, Hu HL, Boonmee S, Doilom M, Chukeatirote E, Bahkali AH, Wang Y, Hyde KD (2011) Astrosphaeriella is polyphyletic, with species in Fissuroma gen. nov., and Neoastrosphaeriella gen. nov. Fungal Divers 51:135–154

    Article  Google Scholar 

  • Liu JK, Phookamsak R, Doilom M, Wiki S, Mei LY, Ariyawansa HA, Boonmee S, Chomnunti P, Dai DQ, Bhat DJ, Romero AI, Xhuang WY, Monkai J, Jones EBG, Chukeatirote E, KoKo TW, Zhoa YC, Wang Y, Hyde KD (2012) Towards a natural classification of Botryosphaeriales. Fungal Divers 57:149–210

    Article  Google Scholar 

  • Liu JK, Phookamsak R, Dai DQ, Tanaka K, Jones EG, Xu JC, Chukeatirote E, Hyde KD (2014) Roussoellaceae, a new pleosporalean family to accommodate the genera Neoroussoella gen. nov., Roussoella and Roussoellopsis. Phytotaxa 181:1–33

    Article  Google Scholar 

  • Liu JK, Hyde KD, Jones EBG, Ariyawansa HA, Bhat DJ, Boonmee S, Maharachchikumbura SSN, McKenzie EHC, Phookamsak R, Phukhamsakda C, Shenoy BD, Abdel-Wahab MA, Buyck B, Chen J, Chethana KWT, Singtripop C, Dai DQ, Dai YC, Daranagama DA, Dissanayake AJ, Doilom M, Dsouza MJ, Fan XL, Goonasekara ID, Hirayama K, Hongsanan S, Jayasiri SC, Jayawardena RS, Karunarathna SC, Li WJ, Mapook A, Norphanphoun C, Pang KL, Perera RH, Persˇoh D, Pinruan U, Senanayake IC, Somrithipol S, Suetrong S, Tanaka K, Thambugala KM, Tian Q, Tibpromma S, Udayanga D, Wijayawardene NN, Wanasinghe DN, Wisitrassameewong K, Zeng XY, Abdel- Aziz FA, Adamčík S, Bahkali AH, Boonyuen N, Bulgakov T, Callac P, Chomnunti P, Greiner K, Hashimoto A, Hofstetter V, Kang JC, Lewis D, Li XH, Liu XZ, Liu ZY, Matsumura M, Mortimer PE, Rambold G, Randrianjohany E, Sato G, Sri-Indrasutdhi V, Tian CM, Verbeken A, von Brackel W, Wang Y, Wen TC, Xu JC, Yan JY, Zhao RL, Camporesi E (2015) Fungal Divers notes 1–110: taxonomic and phylogenetic contributions to fungal species. Fungal Divers 72:1–197

    Article  CAS  Google Scholar 

  • Liu M, Chaverri P, Hodge KT (2006) A taxonomic revision of the insect biocontrol fungus Aschersonia aleyrodis, its allies with white stromata and their Hypocrella sexual states. Mycol Res 110:537–554

    Article  CAS  PubMed  Google Scholar 

  • Liu NG, Ariyawansa HA, Hyde KD, Maharachchikumbura SSN, Zhao RL, Phillips AJL, Jayawardena RS, Thambugala KM, Dissanayake AJ, Wijayawardene NN, Liu JK, Liu ZY, Jeewon R, Jones EBG, Jumpathong J (2016) Perspectives into the value of genera, families and orders in classification. Mycosphere 7:1649–1668

    Google Scholar 

  • Liu Y, Steenkamp ET, Brinkmann H, Forget L, Philippe H, Lang BF (2009) Phylogenomic analyses predict sister group relationship of nucleariids and fungi and paraphyly of zygomycetes with significant support. BMC Evol Biol 9:272

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Liu YJ, Whelen S, Hall BD (1999) Phylogenetic relationships among ascomycetes: evidence from an RNA polymerase II subunit. Mol Biol Evol 16:1799–1808

    Article  CAS  PubMed  Google Scholar 

  • Liu ZY, Liang ZQ, Liu AY, Yao YJ, Hyde KD, Yu ZN (2002) Molecular evidence for teleomorph anamorph connections in Cordyceps based on ITS-5.8S rDNA sequences. Mycol Res 106:1100–1108

    Article  CAS  Google Scholar 

  • Locquin M (1984) Mycologie Générale et Structurale. Masson, Paris

  • Lombard L, Houbraken J, Decock C, Samson RA, Meijer M, Réblová M, Groenewald JZ, Crous PW (2016) Generic hyper-diversity in Stachybotriaceae. Persoonia 36:156–246

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Luangsa-ard JJ, Hywel-Jones NL, Manoch L, Samson RA (2005) On the relationships of Paecilomyces sect. Isarioidea species. Mycol Res 109:581–589

    Article  CAS  PubMed  Google Scholar 

  • Lumbsch HT, Huhndorf SM (2007) Outline of Ascomycota. Myconet 13:1–99

    Google Scholar 

  • Lumbsch HT, Huhndorf SM (2010) Myconet volume 14. Part one. Outline of Ascomycota 2009. Part Two. Notes on Ascomycete systematics. Nos. 4751–5113. Fieldiana Life Earth Sci 1:1–64

    Article  Google Scholar 

  • Maas JL (1998) Compendium of strawberry diseases, 2nd edn. APS Press, St Paul, pp 1–98

    Google Scholar 

  • Maharachchikumbura SSN, Guo LD, Cai L, Chukeatirote E, Wu WP, Sun X, Crous PW, Bhat DJ, McKenzie EHC, Bahkali AH, Hyde KD (2012) A multi-locus backbone tree for Pestalotiopsis, with a polyphasic characterization of 14 new species. Fungal Divers 56:95–129

    Article  Google Scholar 

  • Maharachchikumbura SSN, Guo L-D, Chukeatirote E, Hyde KD (2014a) Improving the backbone tree for the genus Pestalotiopsis; addition of P. steyaertii and P. magna sp. nov. Mycol Prog 3:617–624

    Article  Google Scholar 

  • Maharachchikumbura SSN, Hyde KD, Groenewald JZ, Xu J, Crous PW (2014b) Pestalotiopsis revisited. Stud Mycol 79:121–186

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Maharachchikumbura SSN, Hyde KD, Jones EBG, McKenzie EHC, Huang S-K, Abdel-Wahab MA, Daranagama DA, Dayarathne M, D’souza MJ, Goonasekara ID, Hongsanan S, Jayawardena RS, Kirk PM, Konta S, Liu J-K, Liu Z-Y, Norphanphoun C, Shenoy BD, Xiao Y, Bahkali AH, Kang J, Somrothipol S, Suetrong S, Wen T, Xu J (2015) Towards a natural classification and backbone tree for Sodariomycetes. Fungal Divers 72:199–301

    Article  Google Scholar 

  • Maharachchikumbura SSN, Hyde KD, Jones EBG, McKenzie EHC, Bhat DJ, Dayarathne MC, Huang SK, Norphanphoun C, Senanayake IC, Perera RH, Shang QJ, Xiao YP, D’souza MJ, Hongsanan S, Jayawardena RS, Daranagama DA, Konta S, Goonasekara ID, Zhuang WY, Jeewon R, Phillips AJL, Abdel-Wahab MA, Al-Sadi AM, Bahkali AH, Boonmee S, Boonyuen N, Cheewangkoon R, Dissanayake AJ, Kang JC, Li QR, Liu JK, Liu XZ, Liu ZY, Luangsa-ard JJ, Pang KL, Phookamsak R, Promputtha I, Suetrong S, Stadler M, Wen TC, Wijayawardene NN (2016) Families of Sordariomycetes. Fungal Divers 79:1–317

    Article  Google Scholar 

  • Maharachchikumbura SS, Larignon P, Al-Sadi AM, Zuo-Yi LIU (2017) Characterization of Neopestalotiopsis, Pestalotiopsis and Truncatella species associated with grapevine trunk diseases in France. Phytopathol Mediterr 55(3):380–390

    Google Scholar 

  • Manawasinghe IS, Phillips AJL, Hyde KD, Chethana KWT, Zhang W, Zhao WS, Yan JY, Li XH (2016) Mycosphere Essays 14: assessing the aggressiveness of plant pathogenic Botryosphaeriaceae. Mycosphere 7(7):883–892

    Google Scholar 

  • Manimohan P, Leelavathy KM (1989) Marasmius species new to India. Sydowia 41:185–199

    Google Scholar 

  • Manimohan P, Joseph AV, Leelavathy KM (1995) The genus Entoloma (Agaricales) in Kerala State, India. Mycol Res 99:1083–1097

    Article  Google Scholar 

  • Mantle PG, Hawksworth DL, Pazoutova S, Collinson LM, Rassing BR (2006) Amorosia littoralis gen. sp. nov., a new genus and species name for the scorpinone and caffeine-producing hyphomycete from the littoral zone in The Bahamas. Mycol Res 110(12):1371–1378

    Article  CAS  PubMed  Google Scholar 

  • Mapook A, Boonmee S, Ariyawansa HA, Tibpromma S, Campesori E, Jones EG, Bahkali AH, Hyde KD (2016) Taxonomic and phylogenetic placement of Nodulosphaeria. Mycol Prog 15(4):1–15

    Article  Google Scholar 

  • Martin R, Gazis R, Skaltsas D, Chaverri P, Hibbett D (2015) Unexpected diversity of basidiomycetous endophytes in sapwood and leaves of Hevea. Mycologia 107(2):284–297

    Article  PubMed  Google Scholar 

  • Matheny PB (2005) Improving phylogenetic inference of mushrooms with RPB1 and RPB2 nucleotide sequences (Inocybe; Agaricales). Mol Phylogenet Evol 35:1–20

    Article  CAS  PubMed  Google Scholar 

  • Matheny PB (2009) A phylogenetic classification of the Inocybaceae. McIlvainea 18:11–21

    Google Scholar 

  • Matheny PB, Bougher NL (2006a) The new genus Auritella from Africa and Australia (Inocybaceae, Agaricales): molecular systematics, taxonomy and historical biogeography. Mycol Prog 5:2–17

    Article  Google Scholar 

  • Matheny PB, Bougher NL (2006b) Validation of Auritella. Mycotaxon 98:231–233

    Google Scholar 

  • Matsushima T (1981) Matsushima Mycological Memoirs 2. Matsushima, Kobe, Japan

    Google Scholar 

  • Matsushima T (1983) Matsushima Mycological Memoirs 3. Matsushima, Kobe

    Google Scholar 

  • Mazzer SJ (1976) A monographic study of the genus Pouzarella, a new genus in the Rhodophyllaceae, Agaricales, Basidiomycetes. Bibliotheca Mycologica 46:1–191

    Google Scholar 

  • McNabb RFR (1965) Taxonomic studies on the Dacrymycetaceae. VI. Femsjonia Fries”. NZ J Bot 3(3):223–228

    Article  Google Scholar 

  • McNabb RFR (1973) Taxonomic studies in the Dacrymycetaceae. VIII. Dacrymyces Nees ex Fries. NZ J Bot 11(3):461–524

    Article  Google Scholar 

  • Miller MA, Pfeiffer W, Schwartz T (2010) Creating the CIPRES Science Gateway for inference of large phylogenetic trees. In: Proceedings of the gateway computing environments workshop (GCE). Institute of Electrical and Electronics Engineers, New Orleans, LA, 14 Nov, pp 1–8

  • Miller SL, Buyck B (2002) Molecular phylogeny of the genus Russula in Europe with a comparison of modern infrageneric classifications. Mycol Res 106:259–276

    Article  CAS  Google Scholar 

  • Miller SL, Larsson E, Larsson KH, Verbeken A, Nuytinck J (2006) Perspectives in the new Russulales. Mycologia 98:960–970

    Article  PubMed  Google Scholar 

  • Minnis AM, Kennedy AH, Grenier DB, Palm ME, Rossman AY (2012) Phylogeny and taxonomic revision of the Planistromellaceae including its coelomycetous anamorphs: contributions towards a monograph of the genus Kellermania. Persoonia 29:11–28

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mirza F (1968) Taxonomic investigations on the ascomycetous genus Cucurbitaria. Nova Hedwigia 16:161–213

    Google Scholar 

  • Miyake I (1909) Studies on the parasitic fungi of rice in Japan. Bot Mag Tokyo 23:85–97

    Article  Google Scholar 

  • Mohanan C (2011) Macrofungi of Kerala. KFRI handbook no. 27, Kerala Forest Research Institute, Peechi

  • Moncalvo JM, Vilgalys R, Redhead SA, Johnson JE, James TY, Aime CM, Hofsetter V, Verduin SJ, Larsson E, Baroni TJ, Thorn GR, Jacobsson S, Clémencon H, Miller OK (2002) One hundred and seventeen clades of euagarics. Mol Phylogenet Evol 23:357–400

    Article  CAS  PubMed  Google Scholar 

  • Moncalvo JM, Nilsson RH, Koster B, Dunham SM, Bernauer T, Matheny PB, McLenon T, Margaritescu S, Weiß M, Garnica S, Danell E, Langer G, Langer E, Larsson E, Larsson KH, Vilgalys R (2006) The cantharelloid clade: dealing with incongruent gene trees and phylogenetic reconstruction methods. Mycologia 98:937–948

    Article  PubMed  Google Scholar 

  • Mongkolsamrit S, Luangsa-Ard JJ, Spatafora JW, Sung GH, Hywel-Jones NL (2009) A combined ITS rDNA and β-tubulin phylogeny of Thai species of Hypocrella with non-fragmenting ascospores. Mycol Res 113(6):684–699

    Article  CAS  PubMed  Google Scholar 

  • Monod M (1983) Monographie taxonomique des Gnomoniaceae (Ascomycétes de l’ordre des Diaporthales I). Beihefte Sydowia 9:1–315

    Google Scholar 

  • Moreau PA, Vila J, Aime MC, Antonín V, Horak E, Pérez-Butrόn JL, Richard F, Urban A, Welti S, Vizzini A (2015) Cibaomyces and Cyptotrama, two new genera for Europe, and an emendation of Rhizomarasmius (Basidiomycota, Physalacriaceae). Mycol Prog 14(2):1–16

    Article  Google Scholar 

  • Moore RT (1958) Deuteromycetes I: the complex. Mycologia 50:681–692

    Article  Google Scholar 

  • Morgado LN, Noordeloos ME, Lamoureux Y, Geml J (2013) Multi-gene phylogenetic analyses reveal species limits, phylogeographic patterns, and evolutionary histories of key morphological traits in Entoloma (Agaricales, Basidiomycota). Persoonia Mol Phylogeny Evol Fungi 31:159–178

    Article  CAS  Google Scholar 

  • Morris EF (1972) Costa Rican Hyphomycetes. Mycologia 64:887–896

    Article  Google Scholar 

  • Mugambi GK, Huhndorf SM (2009) Molecular phylogenetics of Pleosporales: Melanommataceae and Lophiostomataceae re-circumscribed (Pleosporomycetidae, Dothideomycetes, Ascomycota). Stud Mycol 64:103–121

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mulenko W, Majewski T, Ruszkiewicz-Michalska M (2008) A preliminary checklist of micromycetes in Poland. W. Szafer Institute of Botany, Polish Academy of Sciences, Krakow

    Google Scholar 

  • Munk A (1953) The system of the Pyrenomycetes. A contribution to a natural classification of the group Sphaeriales sensu Lindau. Dansk Botanisk Arkiv 15:1–163

    Google Scholar 

  • Munk A (1957) Danish Pyrenomycetes. Dan Bot Ark 17:1–491

    Google Scholar 

  • Muñoz JA (2005) Boletus s.l. (excl. Xerocomus). Fungi Europaei 2. Edizioni Candusso, Alassio

  • Murrill WA (1909) The Boletaceae of North America: I. Mycologia 1(1):4–18

    Article  Google Scholar 

  • MycoBank (2017) http://www.mycobank.org/quicksearch.aspx

  • Najafzadeh MJ, Dolatabadi S, Keisari MS, Naseri A, Feng P, De Hoog GS (2013) Detection and identification of opportunistic Exophiala species using the rolling circle amplification of ribosomal internal transcribed spacers. J Microbiol Methods 94:338–342

    Article  CAS  PubMed  Google Scholar 

  • Nannf (1932) Nova Acta Regiae Societatis Scientiarum Upsaliensis 8(2):66

  • Natarajan K, Manjula B (1982) South Indian Agaricales: XI. Mycologia 74:130–137

  • Neubert K, Mendgen K, Brinkmann H, Wirsel SGR (2006) Only a few fungal species dominate highly diverse mycofloras associated with the common reed. Appl Environ Microbiol 72:1118–1128

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Nguyen TTT, Lee SH, Bae S, Jeong SJ, Mun HY, Lee HB (2016) Characterization of two new records of zygomycete species belonging to undiscovered taxa in Korea. Mycobiology 44:29–37

    Article  PubMed  PubMed Central  Google Scholar 

  • Noordeloos ME (1981) Entoloma subgenera Entoloma and Allocybe in the Netherlands and adjacent regions with a reconnaissance of its remaining taxa in Europe. Persoonia 11:153–256

    Google Scholar 

  • Noordeloos ME (1992) Entoloma s.l. Fungi Europaei, vol. 5. Giovanna Biella, Italy

  • Noordeloos ME (2004) Entoloma s.l. Fungi Europaei, vol 5a. Edizione Candusso, Alassio

  • Noordeloos ME (2010) Hoe raak ik thuis in de boleten—8. De roodporieboleten (sectie Luridi). Coolia 53(2):53–71

  • Noordeloos ME, Gates GM (2012) The Entolomataceae of Tasmania. Fungal diversity research series, vol 22. Springer, London

  • Norphanphoun C, Doilom M, Daranagama DA, Phookamsak R, Wen TC, Bulgakov TS, Hyde KD (2017) Revisiting the genus Cytospora and allied species. Mycosphere 8:51–97

    Article  Google Scholar 

  • Núñez M, Ryvarden L (1995) Polyporus (Basidiomycotina) and related genera. Synop Fungorum 10:1–85

    Google Scholar 

  • Nylander JAA, Wilgenbusch JC, Warren DL, Swofford DL (2008) AWTY (are we there yet?): a system for graphical exploration of MCMC convergence in Bayesian phylogenetics. Bioinformatics 24:581–583

    Article  CAS  PubMed  Google Scholar 

  • Oberwinkler F (1993) Diversity and phylogenetic importance of tropical heterobasidiomycetes. Br Mycol Soc Symp 19:121

    Google Scholar 

  • O’Donnell K (1993) Fusarium and its near relatives. Wallingford, UK

    Google Scholar 

  • Olariaga I, Begoña MJ, García-Etxerbarria K, Salcedo I (2009) Species delimitation in the European species of Clavulina (Cantharellales, Basidiomycota) inferred from phylogenetic analyses of ITS region and morphological data. Mycol Res 113:1261–1270

    Article  CAS  PubMed  Google Scholar 

  • Oliveira RJV, Lima TEF, Cunha IB, Coimbra VRM, Silva GA, Bezerra JL, Cavalcanti MAQ (2014) Corniculariella brasiliensis, a new species of coelomycetes in the rhizosphere of Caesalpinia echinata (Fabaceae, Caesalpinioideae) in Brazil. Phytotaxa 178(3):197–204

    Article  Google Scholar 

  • Örstadius L, Ryberg M, Larsson E (2015) Molecular phylogenetics and taxonomy in Psathyrellaceae (Agaricales) with focus on psathyrelloid species: introduction of three new genera and 18 new species. Mycol Prog 14:25

    Article  Google Scholar 

  • Ortiz-Santana B, Lindner DL, Miettinen O, Justo A, Hibbett DS (2013) A phylogenetic overview of the Antrodia clade (Basidiomycota, Polyporales). Mycologia 105:1391–1411

    Article  CAS  PubMed  Google Scholar 

  • Orton PD, Watling R (1979) Coprinaceae 1: Coprinus. British Fungus Flora. Agarics and Boleti 2. Royal Botanic Garden, Edinburgh

  • Padamsee M, Matheny PB, Dentinger BT, McLaughlin DJ (2008) The mushroom family Psathyrellaceae: evidence for large-scale polyphyly of the genus Psathyrella. Mol Phylogenet Evol 46:415–429

    Article  CAS  PubMed  Google Scholar 

  • Page RDM (2001) Tree View: tree drawing software for Apple Macintosh and Windows. http://taxonomy.zoology.gla.ac.uk/rod/treeview.html

  • Palazon FL (2006) Setas para todos. Pirineo, Huesca

  • Pantidou ME (1973) Fungus-host index for Greece. Benaki Phytopathol. Inst., Kiphissia

  • Peever TL, Barve MP, Stone LJ, Kaiser WJ (2007) Evolutionary relationships among Ascochyta species infecting wild and cultivated hosts in the legume tribes Cicereae and Vicieae. Mycologia 99:59–77

    Article  CAS  PubMed  Google Scholar 

  • Pegler DN (1972) A revision of the genus Lepiota from Ceylon. Kew Bull 27:155–202

    Article  Google Scholar 

  • Pegler DN (1977) A preliminary agaric flora of East Africa. Kew Bull Addit Ser 6:1–615

    Google Scholar 

  • Pegler DN (1983) The genus Lentinus: a world monograph. Kew Bull Addit Ser 10:1–281

    Google Scholar 

  • Pegler DN (1986) Agaric flora of Sri Lanka. Kew Bull Addit Ser 12:1–519

    Google Scholar 

  • Peintner U, Knapp M, Fleischer V, Walch G, Dresch P (2016) Myrmecridium hiemale sp nov from snow-covered alpine soil is the first eurypsychrophile in this genus of anamorphic fungi. Int J Syst Evol Microbiol 66(7):2592–2598

    Article  CAS  Google Scholar 

  • Persoon CH (1797) Tentamen dispositionis methodicae fungorum in classes, ordines genera et familias. Lipsiae

  • Petch T (1948) A revision of the Ceylon Marasmii. Trans Br Mycol Soc 31:19–44

    Article  Google Scholar 

  • Petersen RH (1983) Notes on clavarioid fungi XVIII. A preliminary outline of Clavulina in southeastern Australia. Nova Hedwigia 37:19–35

    Google Scholar 

  • Petersen RH (1988) The clavarioid fungi of New Zealand. Bull NZ Dep Ind Res 236:1–170

    Google Scholar 

  • Petersen RH, Hughes KW, Adamčík S, Tkalčec Z, Mešić A (2012) Typification of three European species epithets attributable to Strobilomyces (Boletales). Czech Mycol 64(2):141–163

    Google Scholar 

  • Peterson SW (2000a) Phylogenetic analysis of Penicillium species based on ITS and LSU-rDNA nucleotide sequences. In: Samson RA, Pitt JI (eds) Integration of modern taxonomic methods for Penicillium and Aspergillus classification. Plenum Press, New York, pp 163–178

    Google Scholar 

  • Peterson SW (2000b) Phylogenetic relationships in Aspergillus based on rDNA sequence analysis. In: Samson RA, Pitt JI (eds) Integration of modern taxonomic methods for Penicillium and Aspergillus classification. Plenum Press, New York, pp 323–355

    Google Scholar 

  • Peterson SW (2008) Phylogenetic analysis of Aspergillus species using DNA sequences from four loci. Mycologia 100:205–226

    Article  CAS  PubMed  Google Scholar 

  • Petrak F, Deighton FC (1952) Beiträge zur Pilzeflora von Sierra Leone. Sydowia 6:309–322

    Google Scholar 

  • Petrini LE (2013) Rosellinia—a world monograph. Bibl Mycol 205:1–410

    Google Scholar 

  • Peyronel B, Dal Vesco G (1955) Ricerche sulla microflora di un terreno agrario presso Torino. Allionia 2:357–417

    Google Scholar 

  • Phillips AJL, Alves A, Pennycook SR, Johnston PR, Ramaley A, Akulov A, Crous PW (2008) Resolving the phylogenetic and taxonomic status of dark-spored teleomorph genera in the Botryosphaeriaceae. Persoonia Mol Phylogeny Evol Fungi 21:29–55

    Article  CAS  Google Scholar 

  • Phillips AJL, Alves A, Abdollahzadeh J, Slippers B, Wingfield MJ, Groenewald JZ, Crous PW (2013) The Botryosphaeriaceae: genera and species known from culture. Stud Mycol 76:51–167

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Phookamsak R, Liu JK, McKenzie EHC, Manamgoda DS, Ariyawansa HA, Thambugala KM, Dai DQ, Camporesi E, Chukeatirote E, Wijayawardene NN, Bahkali AH, Mortimer PE, Xu JC, Hyde KD (2014) Revision of Phaeosphaeriaceae. Fungal Divers 68:159–238

    Article  Google Scholar 

  • Phookamsak R, Norphanphoun C, Tanaka K, Dai DQ, Luo ZL, Liu JK, Su HY, Bhat DJ, Bahkali AH, Mortimer PE, Xu JC, Hyde KD (2015) Towards a natural classidication of Astrosphaeriella-like species; introducing Astrosphaeriellaceae and Pseudoastrosphaeriellaceae fam. nov and Astrosphaeriellaceaeopsis, gen. nov. Fungal Divers 74:143–197

    Article  Google Scholar 

  • Phukhamsakda C, Hongsanan S, Ryberg M, Ariyawansa HA, Chomnunti P, Bahkali AH, Hyde KD (2016) The evolution of Massarineae with Longipedicellataceae fam. nov. Mycosphere 7:1713–1731

    Google Scholar 

  • Pici G (1955) Qualche osservazione sopra due Mucoraceae. Atti Inst Bot Univ Pavia 13:38–44

    Google Scholar 

  • Pinnoi A, Jeewon R, Sakayaroj J, Hyde KD, Jones EG (2007) Berkleasmium crunisia sp. nov. and its phylogenetic affinities to the Pleosporales based on 18S and 28S rDNA sequence analyses. Mycologia 99:378–384

    Article  CAS  PubMed  Google Scholar 

  • Pitt JI (1980) The genus Penicillium and its teleomorphic states Eupenicillium and Talaromyces. Academic Press, London

    Google Scholar 

  • Põldmaa K (2011) Tropical species of Cladobotryum and Hypomyces producing red pigments. Stud Mycol 31(68):1–34

    Article  Google Scholar 

  • Pradeep CK, Vrinda KB (2010) Ectomycorrhizal fungal diversity in three different forest types and their association with endemic, indigenous and exotic species in the Western Ghat forests of Thiruvananthapuram district, Kerala. J Mycopathol Res 48:279–289

    Google Scholar 

  • Pratibha J, Prabhugaonkar A, Hyde KD, Bhat DJ (2014) Phylogenetic placement of Bahusandhika, Cancellidium and Pseudoepicoccum (asexual Ascomycota). Phytotaxa 176:68–80

    Article  Google Scholar 

  • Promputtha I, Lumyong S, Dhanasekaran V, McKenzie EHC, Hyde KD, Jeewon R (2007) A phylogenetic evaluation of whether endophytes become saprotrophs at host senescence. Microb Ecol 53(4):579–590

    Article  PubMed  Google Scholar 

  • Qin J, Yang ZL (2016) Cyptotrama (Physalacriaceae, Agaricales) from Asia. Fungal Biol 120:513–529

    Article  PubMed  Google Scholar 

  • Qu C, Yin G, Zhao G, Cui B, Liu X (2014) Three new species of Berkleasmium (Hyphomycetes) from China. Nova Hedwigia 98:151–161

    Article  Google Scholar 

  • Quaedvlieg W, Verkley GJM, Shin H-D, Barretto RW, Alfenas AC, Swart WJ, Groenewald JZ, Crous PW (2013) Sizing up Septoria. Stud Mycol 75:307–390

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Rabenhorst (1858) Herb. Myc. Ed., 2:725

  • Rambaut A (2014) FigTree v1.4: tree figure drawing tool. http://treebio.ed.ac.uk/software/figtree/

  • Rambaut A, Drummond AJ (2003) Tracer: MCMC trace analysis tool. University of Oxford, Oxford

    Google Scholar 

  • Rannala B, Yang Z (1996) Probability distribution of molecular evolutionary trees: a new method of phylogenetic inference. J Mol Evol 43:304–311

    Article  CAS  PubMed  Google Scholar 

  • Rao PR, Rao D (1963) Berkleasmium zobel from India. Mycopathologia 22:311–314

    Google Scholar 

  • Read SJ, Jones EBG, Moss ST (1997) Ultrastructural observation of asci, ascospores and appendages of Massarina armatispora (Ascomycota). Mycoscience 38:141–146

    Article  Google Scholar 

  • Réblová M, Gams W, Seifert KA (2011) Monilochaetes and allied genera of the Glomerellales, and a reconsideration of families in the Microascales. Stud Mycol 68:163–191

    Article  PubMed  PubMed Central  Google Scholar 

  • Réblová M, Fournier J, Štěpánek V (2016) Two new lineages of aquatic ascomycetes: Atractospora gen. nov. and Rubellisphaeria gen. et sp. nov., and a sexual morph of Myrmecridium montsegurinum sp. nov. Mycol Prog 15(3):1–18

  • Redhead SA, Ginns J (1980) Cyptotrama asprata (Agaricales) from North America and notes on the five other species of Cyptotrama sect. Xerulina. Can J Bot 58(6):731–740

    Article  Google Scholar 

  • Redhead SA, Ginns JH (1985) A reappraisal of agaric genera associated with brown rots of wood. Trans Mycol Soc Jpn 26:349–381

    Google Scholar 

  • Redhead SA, Vilgalys R, Moncalvo JM, Johnson J, Hopple JS Jr (2001) Coprinus Pers. and the disposition of Coprinus species sensu lato. Taxon 50:203–241

    Article  Google Scholar 

  • Rehner SA (2001) Primers for elongation factor 1-alpha (EF1-alpha). http://www.aftol.org/pdfs/EF1primer.pdf

  • Rehner SA, Samuels GJ (1995) Molecular systematics of the Hypocreales: a teleomorph gene phylogeny and the status of their anamorphs. Can J Bot 31(73):816–823

    Article  Google Scholar 

  • Ribaldi MS (1952) Sopra un interessante Zigomicete terricolo: Gongronella urceolifera n. gen. et n. sp. Riv Biol 49:157–166

    Google Scholar 

  • Rogerson CT (1970) The hypocrealean fungi (ascomycetes, Hypocreales). Mycologia 1:865–910

    Article  Google Scholar 

  • Romagnesi H (1967) Les Russules d’Europe et d’Afrique du Nord. Bordas, Paris

    Google Scholar 

  • Romagnesi H (1978) les fondements de la taxonomie des rhodophylles et leur classification. Nova Hedwigia 59:1–80

    Google Scholar 

  • Ronquist F, Huelsenbeck JP (2003) MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics 19:1572–1574

    Article  CAS  PubMed  Google Scholar 

  • Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Höhna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP (2012) MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Syst Biol 61:539–542

    Article  PubMed  PubMed Central  Google Scholar 

  • Rossman AY, Farr DF, Castlebury LA (2007) A review of the phylogeny and biology of the Diaporthales. Mycoscience 48:135–144

    Article  Google Scholar 

  • Rossman AY, Crous PW, Hyde KD, Hawksworth DL, Aptroot A, Bezerra JL, Bhat JD, Boehm E, Braun U, Boonmee S, Camporesi E, Chomnunti P, Dai DQ, D’souza MJ, Dissanayake A, Jones EBG, Groenewald JZ, Hernández-Restrepo M, Hongsanan S, Jaklitsch WM, Jayawardena R, Li WJ, Kirk PM, Lawrey JD, Mapook A, McKenzie EHC, Monkai J, Phillips AJL, Phookamsak R, Raja HA, Seifert KA, Senanayake IC, Slippers B, Suetrong S, Taylor JE, Thambugala KM, Tian Q, Tibpromma S, Wanasinghe DN, Wijayawardene NN, Wikee S, Woudenberg JHC, Wu HX, Yan J, Yang T, Zhang Y (2015) Recommended names for pleomorphic genera in Dothideomycetes. IMA Fungus 6:507–523

    Article  PubMed  PubMed Central  Google Scholar 

  • Ruiz Fernandez JM, Ruiz Pastor E (2006) Guia Micologica Tomo n. 4, Supl. Orden Boletales en España, Imagen. Bilbao: 62

  • Rungjindamai N, Pinruan U, Choeyklin R, Hattori T, Jones EBG (2008) Molecular characterization of basidiomycetous endophytes isolated from leaves, rachis and petioles of the oil palm, Elaeis guineensis, in Thailand. Fungal Divers 33:139–161

    Google Scholar 

  • Ryvarden L (1991) Genera of polypores, nomenclature and taxonomy. Synop Fungorum 5:1–363

    Google Scholar 

  • Ryvarden L, Gilbertson RE (1984) Mycotaxon 19:141

  • Ryvarden L, Gilbertson RL (1993) European polypores 1. Abortiporus-Lindtneria. Synop Fungorum 6:1–387

    Google Scholar 

  • Ryvarden L, Gilvertson RL (1994) European polypores, part 2. Fungiflora, Oslo

    Google Scholar 

  • Saccardo PA (1878) Fungi Veneti novi vel critici vel mycologiae Venetae addendi. Ser. IX. Michelia 1(4):407

    Google Scholar 

  • Saccardo PA (1880) Conspectus generum fungorum italiae inferiorum nempe ad Sphaeropsideas, Melanconieas et Hyphomyceteas pertinentium, systemate sporologico dispositu. Michelia 2:1–38

    Google Scholar 

  • Saccardo PA (1882) Fungi Gallici lecti a Cl. viris P. Brunaud, C.C. Gillet, Abb. Letendre, A. Malbranche, J. Therry & Dom. Libert. Series IV. Michelia 2(8):583–648

  • Saccardo PA (1892) Supplementum Universale, Pars II. Discomyceteae-Hyphomyceteae. Sylloge Fungorum 10:1–964

    Google Scholar 

  • Saccardo PA (1899) Sylloge fungorum 14:1–1316

  • Samson RA, Seifert KA, Kuijpers AFA, Houbraken JAMP, Frisvad JC (2004) Phylogenetic analysis of Penicillium subgenus Penicillium using partial β-tubulin sequences. Stud Mycol 49:175–200

    Google Scholar 

  • Samson RA, Houbraken J, Varga J, Frisvad JC (2009) Polyphasic taxonomy of the heat resistant ascomycete genus Byssochlamys and its Paecilomyces anamorphs. Persoonia 22:14–27

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Samson RA, Houbraken J, Thrane U (2010) Food and indoor fungi. CBS KNAW Biodiversity Center, Utrecht

    Google Scholar 

  • Santiago ALCMA, Santos PJP, Maia LC (2013) Mucorales from the semiarid of Pernambuco, Brazil. Braz J Microbiol 44:299–305

    Article  Google Scholar 

  • Sarnari M (1998) Monografia illustrate de genere Russula in Europa. Tomo Primo. AMB, Centro Studi Micologici, Trento

    Google Scholar 

  • Sarnari M (2005) Monografia illustrate de genere Russula in Europa. Tomo Secondo. AMB, Centro Studi Micologici, Trento

    Google Scholar 

  • Sarycheva LA, Svetasheva TY (2015) Boletus legaliae Pilát//Red Data Book of Lipetsk region. Plants, fungi, lichenes, 2nd edn. Lipetsk:536–537 (in Russian)

  • Sato H, Hattori T, Kurogi S, Yumoto T (2005) Strobilomyces mirandus Corner, a new record from Japan. Mycoscience 46:102–105

    Article  Google Scholar 

  • Schardl CL, Young CA, Hesse U, Amyotte SG, Andreeva K, Calie PJ, Fleetwood DJ, Haws DC, Moore N, Oeser B, Panaccione DG (2013) Plant-symbiotic fungi as chemical engineers: multi-genome analysis of the Clavicipitaceae reveals dynamics of alkaloid loci. PLoS Genet 9(2):e1003323

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Schipper MAA, Samson RA (1978) One certain species of Mucor with a key to all accepted species. Stud Mycol 17:1–52

    Google Scholar 

  • Schoch CL, Shoemaker RA, Seifert KA, Hambleton S, Spatafora JW, Crous PW (2006) A multigene phylogeny of the Dothideomycetes using four nuclear loci. Mycologia 98:1041–1052

    Article  CAS  PubMed  Google Scholar 

  • Schoch CL, Crous PW, Groenewald JZ, Boehm EWA, Burgess TI, de Gruyter J, de Hoog GS, Dixon LJ, Grube M, Gueidan C, Harada Y, Hatakeyama S, Hirayama K, Hosoya T, Huhndorf SM, Hyde KD, Jones EBG, Kohlmeyer J, Kruys A, Li YM, Lücking R, Lumbsch HT, Marvanová L, Mbatchou JS, McVay AH, Miller AN, Mugambi GK, Muggia L, Nelsen MP, Nelson P, Owensby CA, Phillips AJL, Phongpaichit S, Pointing SB, Pujade-Renaud V, Raja HA, Rivas Plata E, Robbertse B, Ruibal C, Sakayaroj J, Sano T, Selbmann L, Shearer CA, Shirouzu T, Slippers B, Suetrong S, Tanaka K, Volkmann-Kohlmeyer B, Wingfield MJ, Wood AR, Woudenberg JHC, Yonezawa H, Zhang Y, Spatafora JW (2009) A class-wide phylogenetic assessment of Dothideomycetes. Stud Mycol 64:1–15

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Schulzer S (1870) Mykologische Beiträge. Verhandlungen der Zoologisch-Botanischen Gesellschaft Wien 20:635–658

    Google Scholar 

  • Seelan JSS, Justo A, Nagy LG, Grand EA, Redhead SA, Hibbett D (2015) Phylogenetic relationships and morphological evolution in Lentinus, Polyporellus and Neofavolus, emphasizing southeastern Asian taxa. Mycologia 107:460–474

    Article  PubMed  Google Scholar 

  • Seifertk K, Morgan-Jones G, Gams W, Kendrick B (2011) The genera of Hyphomycetes. CBS-KNAW Fungal Biodiversity Centre, Utrecht

    Google Scholar 

  • Senanayake IC, Maharachchikumbura SSN, Hyde KD, Bhat JD, Jones EBG, McKenzie EHC, Dai DQ, Daranagama DA, Dayarathne MC, Goonasekara ID, Konta S, Li WJ, Shang QJ, Stadler M, Wijayawardene NN, Xiao YP, Norphanphoun C, Li QR, Liu XZ, Bahkali AH, Kang JC, Wang Y, Wen TC, Wendt L, Xu JC, Camporesi E (2015) Towards unraveling relationships in Xylariomycetidae (Sordariomycetes). Fungal Divers 73:73–144

    Article  Google Scholar 

  • Senanayake IC, Maharachchikumbura SSN, Jeewon R, Promputtha I, Al-Sadi AM, Camporesi E, Hyde KD (2017) Morphophylogenetic study of Sydowiellaceae reveals several new genera. Mycosphere 8(1):172–217

    Article  Google Scholar 

  • Seyedmousavi S, Badali H, Chlebicki A, Zhao J, Prenafeta-Boldú FX, de Hoog GS (2011) Exophiala sideris, a novel black yeast isolated from environments polluted with toxic alkyl benzenes and arsenic. Fungal Biol 115:1030–1037

    Article  CAS  PubMed  Google Scholar 

  • Shearer CA, Raja HA, Miller AN, Nelson P, Tanaka K, Hirayama K, Marvanova L, Hyde KD, Zhang Y (2009) The molecular phylogeny of freshwater Dothideomycetes. Stud Mycol 64:145–153

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Shenoy BD, Jeewon R, Wu WP, Bhat DJ, Hyde KD (2006) Ribosomal and RPB2 DNA sequence analyses suggest that Sporidesmium and morphologically similar genera are polyphyletic. Mycol Res 110:916–928

    Article  CAS  PubMed  Google Scholar 

  • Shoemaker RA (1984) Canadian and some extralimital Nodulosphaeria and Entodesmium species. Can J Bot 62:2730–2753

    Article  Google Scholar 

  • Shoemaker RA, Babcock CE (1989) Phaeosphaeria. Can J Bot 67:1500–1599

    Article  Google Scholar 

  • Shirouzu T, Hirose D, Tokumasu S (2009) Taxonomic study of the Japanese Dacrymycetes. Persoonia 23:16

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Silvestro D, Michalak I (2010) raxmlGUI: a graphical front-end for RAxML. http://sourceforge.net/projects/raxmlgui/

  • Silvestro D, Michalak I (2012) RaxmlGUI: a graphical front-end for RAxML. Org Divers Evol 12:335–337

    Article  Google Scholar 

  • Simon UK, Bauer R, Rioux D, Simard M, Oberwinkler F (2005a) The intercellular biotrophic leaf pathogen Cymadothea trifolii locally degrades pectins, but not cellulose or xyloglucan in cell walls of Trifolium repens. New Phytol 165:243–260

    Article  CAS  PubMed  Google Scholar 

  • Simon UK, Bauer R, Rioux D, Simard M, Oberwinkler F (2005b) The vegetative life-cycle of the clover pathogen Cymadothea trifolii as revealed by transmission electron microscopy. Mycol Res 109:764–778

    Article  PubMed  Google Scholar 

  • Simon UK, Groenewald JZ, Crous PW (2009) Cymadothea trifolii, an obligate biotrophic leaf parasite of Trifolium, belongs to Mycosphaerellaceae as shown by nuclear ribosomal DNA analyses. Persoonia 22:49–55

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Simonini G (1992) Il valore statistico delle dimensioni sporali nei boleti. Atti riguardanti il V Seminario su Russulales e Boletales. AMB Reggio Emilia:16–28

  • Simonini G (1998) Una metodologia per la descrizione e la rappresentazione delle dimensioni sporali (Applicata al caso delle Boletaceae). Pagine di Micologia 9:1–24

    Google Scholar 

  • Simonyan SA (1981) Mycoflora of botanical gardens and arboreta in Armenia. Hayka:232

  • Singer R (1965) Die Röhrlinge, Teil I. J. Klinkhartdt. Bad Heilbrunn:131

  • Singer R (1967) Die Röhrlinge, Teil II, J. Klinkhartdt. Bad Heilbrunn:151

  • Singer R (1975) The Agaricales in modern taxonomy, 3rd edn. J. Cramer, Vaduz

    Google Scholar 

  • Singer R (1976) Marasmieae (Basidiomycetes-Tricholomataceae). Flora Neotropica Monogr 17:1–347

    Google Scholar 

  • Singer R (1986) The Agaricales in modern taxonomy, 4th edn. Sven Koeltz Scientific Books, Königstein

    Google Scholar 

  • Sivanesan A (1984) The bitunicate ascomycetes and their anamorphs. J Cramer, Vaduz

  • Slippers B, Wingfield MJ (2007) Botryosphaeriaceae as endophytes and latent pathogens of woody plants: diversity, ecology and impact. Fungal Biol Rev 21(2):90–106

    Article  Google Scholar 

  • Slippers B, Boissin E, Phillips A, Groenewald J, Lombard L, Wingfield M, Postma A, Burgess T, Crous P (2013) Phylogenetic lineages in the Botryosphaeriales: a systematic and evolutionary framework. Stud Mycol 76:31–49

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sogonov MV, Castlebury LA, Rossman AY, Mejía LC, White JF Jr (2008) Leaf-inhabiting genera of the Gnomoniaceae, Diaporthales. Stud Mycol 62:1–77

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sotome K, Hattori T, Kakishima M (2007) Polyporus phyllostachydis sp. nov. with notes on other rhizophilic species of Polyporus (Basidiomycota, Polyporaceae). Mycoscience 48:42–46

    Article  Google Scholar 

  • Sotome K, Hattori T, Ota Y, To-anun C, Salleh B, Kakishima M (2008) Phylogenetic relationships of Polyporus and morphologically allied genera. Mycologia 100:603–615

    Article  CAS  PubMed  Google Scholar 

  • Sotome K, Hattori T, Ota Y (2011) Taxonomic study on a threatened polypore, Polyporus pseudobetulinus, and a morphologically similar species, P. subvarius. Mycoscience 52:319–326

    Article  Google Scholar 

  • Sotome K, Akagi Y, Lee SS, Ishikawa NK, Hattori T (2013) Taxonomic study of Favolus and Neofavolus gen. nov. segregated from Polyporus (Basidiomycota, Polyporales). Fungal Divers 58:245–266

    Article  Google Scholar 

  • Spatafora JW, Chang Y, Benny GL, Lazarus K, Smith ME, Berbee ML, Bonito G, Corradi N, Grigoriev I, Gryganskyi A, James TY (2016) A phylum-level phylogenetic classification of zygomycete fungi based on genome-scale data. Mycologia 108(5):1028–1046

    Article  PubMed  Google Scholar 

  • Spegazzini C (1910) Mycetes Argentinenses (series V). Anales Mus Nac Hist Nat Buenos Aires 20(13):329–467

  • Spegazzini C (1911) Hermatomyces Speg. Anales Mus Nac Hist Nat Buenos Aires 20(13):445

  • Spielman LJ (1985) A monograph of Valsa on hardwoods in North America. Can J Bot 63(8):1355–1378

    Article  Google Scholar 

  • Stadler M, Kuhnert E, Peršoh D, Fournier J (2013) The Xylariaceae as model example for a unified nomenclature following the “One Fungus-One Name” (1F1N) concept. Mycology 4:5–21

    CAS  Google Scholar 

  • Stamatakis A (2006) RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics 22:2688–2690

    Article  CAS  PubMed  Google Scholar 

  • Stamatakis A (2014) RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics 30(9):1312–1313

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Stevens NE (1926) Two species of Physalospora on citrus and other hosts. Mycologia 18:206–217

    Article  Google Scholar 

  • Steyaert RL (1949) Contributions á lé tude monographique de Pestalotia de Not. et Monochaetia Sacc. (Truncatella gen. nov. et Pestalotiopsis gen. nov.). Bulletin du Jardin botanique de l’É tat a Bruxelles 19:285–354

  • Stiller JW, Hall BD (1997) The origin of red algae: Implications for plastid evolution. Proc Natl Acad Sci USA 94(9):4520–4525

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Stukenbrock EH, Banke S, McDonald BA (2006) Global migration patterns in the fungal wheat pathogen Phaeosphaeria nodorum. Mol Ecol 15:2895–2904

    Article  PubMed  Google Scholar 

  • Sudhadham M, Prakitsin S, Sivichai S, Chaiyarat R, Dorrestein GM, Menken SBJ, De Hoog G (2008) The neurotropic black yeast Exophiala dermatitidis has a possible origin in the tropical rain forest. Stud Mycol 61:145–155

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Suetrong S, Schoch CL, Spatafora JW, Kohlmeyer J, Volkmann-Kohlmeyer B, Sakayaroj J, Phongpaichit S, Tanaka K, Hirayama K, Jones EBG (2009) Molecular systematics of the marine Dothideomycetes. Stud Mycol 64:155–173

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Sung G, Hywel-Jones NL, Sung J-M, Luangsa-Ard JJ, Shrestha B, Spatafora JW (2007) Phylogenetic classification of Cordyceps and the clavicipitaceous fungi. Stud Mycol 57:5–59

    Article  PubMed  PubMed Central  Google Scholar 

  • Sutton BC (1980) The Coelomycetes. Fungi imperfecti with pycnidia, acervuli and stromata. Commonwealth Mycological Institute, Kew

  • Svetasheva TY (2010) Boletus legaliae Pilát//Red Data Book of Tula region: plants and fungi./Tula Region Administration, Department of the Tula Region on ecology and natural resources—Tula, Grif et K:327 (in Russian)

  • Svetasheva TY, Kovalenko AE (2013) Boletus rubrosanguineus Cheype//Red Data Book of Karachay-Cherkessia Republic—Cherkessk:201 (in Russian)

  • Swofford DL (2003) PAUP: phylogenetic analysis using parsimony, version 4.0 b10. Sinauer Associates, Sunderland, MA. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348772

  • Sydow H (1928) Fungi Chilenses a cl. E. Werdermann lecti. Pars prima. Ann Mycol 26(1–2):100–126

  • Tamura K, Stecher G, Peterson D, Filipski A, Kumar S (2013) MEGA6: molecular evolutionary genetics analysis version 6.0. Mol Biol Evol 30:2725–2729

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tan YS, Desjardin DE, Perry BA, Vikineswary S, Noorlidah A (2009) Marasmius sensu stricto in Peninsular Malaysia. Fungal Divers 37:9–100

    Google Scholar 

  • Tanaka K, Hirayama K, Yonezawa H, Sato G, Toriyabe A, Kudo H, Hashimoto A, Matsumura M, Harada Y, Kurihara Y, Shirouzu T (2015) Revision of the Massarineae (Pleosporales, Dothideomycetes). Stud Mycol 82:75–136

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tang AMC, Hyde KD, Corlett RT (2003) Diversity of fungi on wild fruits in Hong Kong. Fungal Divers 14:165–185

    Google Scholar 

  • Tang AMC, Jeewon R, Hyde KD (2009) A re-evaluation of the evolutionary relationships within the Xylariaceae based on ribosomal and protein-coding gene sequences. Fungal Divers 34:127–155

    Google Scholar 

  • Templeton MD, Rikkerink EHA, Solon SL, Crowhurst RN (1992) Cloning and molecular characterisation of the glyceraldehyde-3-phosphate dehydrogenase-encoding gene and cDNA from the plant pathogenic fungus Glomerella cingulata. Gene 122:225–230

    Article  CAS  PubMed  Google Scholar 

  • Tennakoon DS, Hyde KD, Phookamsak R, Wanasinghe DN, Camporesi E, Promputtha I (2016) Taxonomy and Phylogeny of Juncaceicola gen. nov. (Phaeosphaeriaceae, Pleosporinae, Pleosporales). Cryptogam Mycol 37:135–156

    Article  Google Scholar 

  • Thacker JR, Henkel TW (2004) New species of Clavulina from Guyana. Mycologia 96:650–657

    Article  PubMed  Google Scholar 

  • Thambugala KM, Daranagama DA, Camporesi E, Singtripop C, Liu ZY, Hyde KD (2014a) Multi-locus phylogeny reveals the sexual state of Tiarosporella in Botryosphaeriaceae. Cryptogam Mycol 35:359–367

    Article  Google Scholar 

  • Thambugala KM, Ariyawansa HA, Li YM, Boonmee S, Hongsanan S, Tian Q, Singtripop C, Bhat DJ, Camporesi E, Jayawardena R, Liu ZY, Xu JC, Chukeatirote E, Hyde KD (2014b) Dothideales. Fungal Divers 68:105–158

    Article  Google Scholar 

  • Thambugala KM, Hyde KD, Tanaka K, Tian Q, Wanasinghe DN, Ariyawansa HA, Jayasiri SC, Boonmee S, Camporesi E, Hashimoto A, Hirayama K, Schumacher RK, Promputtha I, Liu ZY (2015a) Towards a natural classification and backbone tree for Lophiostomataceae, Floricolaceae, and Amorosiaceae fam. nov. Fungal Divers 74:199–266

    Article  Google Scholar 

  • Thambugala KM, Chunfang Y, Camporesi E, Bahkali AH, Liu ZY, Hyde KD (2015b) Pseudodidymosphaeria gen. nov. in Massarinaceae. Phytotaxa 231:271–282

    Article  Google Scholar 

  • Thambugala KM, Bulgakov TS, Eungwanichayapant PD, Liu ZY, Hyde KD (2016) Camarosporium uniseriatum nom. nov., from Celtis occidentalis in European Russia. Stud Fungi 1:90–98

    Google Scholar 

  • Theissen F (1913) Lembosia-Studien. Ann Mycol 11(5):424–467

    Google Scholar 

  • Thilagam L, Nayak BK, Nanda A (2015) Studies on the diversity of coprophilous microfungi from hybrid cow dung samples. Int J PharmTech Res 8:135–138

    Google Scholar 

  • Tian Q, Liu JK, Hyde KD, Wanasinghe DN, Boonmee S, Jayasiri SC, Luo ZL, Taylor JE, Phillips AJL, Bhat DJ, Li WJ, Ariyawansa H, Thambugala KM, Jones EBG, Chomnunti P, Bahkali AH, Xu JC, Camporesi E (2015) Phylogenetic relationships and morphological reappraisal of Melanommataceae (Pleosporales). Fungal Divers 74:267–324

    Article  Google Scholar 

  • Tibpromma S, Wijayawardene NN, Manamgoda DS, Boonmee S, Wanasinghe DN, Camporesi E, Yang JB, Hyde KD (2016a) Camarosporium arezzoensis on Cytisus sp., an addition to sexual state of Camarosporium sensu stricto. Saudi. J Biol Sci 23(1):1–8

    Google Scholar 

  • Tibpromma S, Bhat J, Doilom M, Lumyong S, Nontachaiyapoom S, Yang JB, Hyde KD (2016b) Three new Hermatomyces species (Lophiotremataceae) on Pandanus odorifer from Southern Thailand. Phytotaxa 275(2):127–139

    Article  Google Scholar 

  • Tode HJ (1790) Fungi Mecklenburgenses Selecti. Fasc. 1. Nova Fungorum Genera Complectens. i–viii, 1–50, plates:1–7

  • Trevisan V (1877) Note sur la tribu des Platystomees de la famille des Hypoxylacées. Bull Soc R Bot Belg 16:14–20

    Google Scholar 

  • Truszkowska W, Chlebicki A (1983) Pyrenomycetes pogorza cieszynskiego. I. Acta Mycol 19:3–19

    Article  Google Scholar 

  • Tulasne R, Tulasne C (1963) Selecta Fungorum Carpologia 2:1–316

  • Tulloss RE (1994) Type studies in Amanita section Vaginatae I: some taxa described in this century (studied 1–23) with notes on description of basidiospores and refractive hyphae in Amanita. Mycotaxon 52:305–396

    Google Scholar 

  • Tulloss RE (2001) Amanita olivaceogrisea a little-known species found in Britain. Field Mycol 2(3):99–100

    Article  Google Scholar 

  • Tulloss RE, Moses E (1995) Amanita populiphila a new species from the central United States. Mycotaxon 53:455–466

    Google Scholar 

  • Tulloss RE, Traverso M (2000) Illustrazioni di una nuova specie di Amanita dedicata al dr. Cornelis Bas di Leiden. Bolletino del Gruppo Micologico G. Bresadola 43(2):151–153

  • Tulloss RE, Traverso M (2001) Amanita basiana a new species from pure Pinus forest and resembling the Alnus-associated species Amanita friabilis. Mycotaxon 77:47–55

    Google Scholar 

  • Tulloss RE, Yang ZL (eds) (2016) Studies in the Amanitaceae. www.amanitaceae.org

  • Tulloss RE, Kuyper TW, Vellinga EC, Yang ZL, Halling RE, Geml J, Sánchez-Ramírez S, Gonçalves SC, Hess J, Pringle A (2016) The genus Amanita should not be split. Amanitaceae 1(3):1–16

    Google Scholar 

  • Uehling JK, Henkel TW, Aime MC, Smith ME (2012a) New species of Clavulina with effused or resupinate basidiomata from the Guiana Shield. Mycologia 104:547–556

    Article  PubMed  Google Scholar 

  • Uehling JK, Henkel TW, Aime MC, Vilgalys R, Smith ME (2012b) New species and distribution records for Clavulina (Cantharellales, Basidiomycota) from the Guiana Shield, with a key to the lowland neotropical taxa. Fungal Biol 116:1263–1274

    Article  PubMed  Google Scholar 

  • Uljé CB (2005) 1. Coprinus Pers. In: Noordeloos ME, Kuyper TW, Vellinga EC (eds) Flora Agaricina Neerlandica 6. Taylor & Francis, Boca Raton, pp 22–109

  • Untereiner WA, Strauss NA, Malloch D (1995) A molecular-morphotaxonomic approach to the systematics of the Herpotrichiellaceae and allied black yeasts. Mycol Res 99:897–913

    Article  CAS  Google Scholar 

  • Upadhyay HP (1969) Soil fungi from north-east and north Brazil-VII. The genus Gongronella. Nova Hedwigia 17:65–73

    Google Scholar 

  • Vasquez G (2012) Indagini micologiche sulle Boletales del territorio siciliano. Annales Confederationis Europaeae Mycologiae Mediterraneensis 2009. Alaimo, Palermo, pp 69–81

  • Vasquez G (2013) Indagini micologiche sulle Boletales Epigee del territorio siciliano—mappatura e censimento delle specie. Tesi di Dottorato di Ricerca (PhD thesis), XXVI Ciclo. Università degli Studi di Catania

  • Vasquez G (2014) Indagini Micologiche sulle Boletales Epigee del Terittorio Siciliano-mappatura e censimento delle specie [doctoral thesis]. Univ Studi Catania, Catania

    Google Scholar 

  • Vellinga EC (2004) Genera in the family Agaricaceae-evidence from nrITS and nrLSU sequences. Mycol Res 108:354–377

    Article  CAS  PubMed  Google Scholar 

  • Velmurugan P, Kamala-Kannan S, Balachandar V, Lakshmanaperumalsamy P, Chae JC, Oh BT (2010) Natural pigment extraction from five filamentous fungi for industrial applications and dyeing of leather. Carbohydr Polym 79(2):262–268

    Article  CAS  Google Scholar 

  • Vilgalys R, Hester M (1990) Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species. J Bacteriol 172:4238–4246

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Visagie CM, Houbraken J, Frisvad JC, Hong SB, Klaassen CHW, Perrone G, Seifert KA, Varga J, Yaguchi T, Samson RA (2014) Identification and nomenclature of the genus Penicillium. Stud Mycol 78:343–371

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Visagie CM, Seifert KA, Houbraken J, Samson RA, Jacobs K (2016) A phylogenetic revision of Penicillium sect. Exilicaulis, including nine new species from fynbos in South Africa. IMA Fungus 7:75–117

    Article  PubMed  PubMed Central  Google Scholar 

  • von Arx JA, Müller E (1954) Die Gattungen der amerosporen Pyrenomyceten. Beiträge zur Kryptogamenflora der Schweiz 11(1):1–434

    Google Scholar 

  • von Arx JA, Muller E (1975) A re-evaluation of the bitunicate ascomycetes with keys to families and genera. Stud Mycol 9:1–159

    Google Scholar 

  • Vrinda KB, Pradeep CK, Abraham TK (1997) Some Inocybes new to India. J Econ Taxon Bot 21(1):41–45

    Google Scholar 

  • Walker DM, Castlebury LA, Rossman AY, Sogonov MV, White JF (2010) Systematics of genus Gnomoniopsis (Gnomoniaceae, Diaporthales) based on a three gene phylogeny, host associations and morphology. Mycologia 102(6):1479–1496

    Article  PubMed  Google Scholar 

  • Walther G, Pawłowska J, Alastruey-IzquierdoA WM, Rodriguez- Tudela JL, Dolatabadi S, Chakrabarti A, de Hoog GS (2013) DNA barcoding in Mucorales: an inventory of biodiversity. Persoonia 30:11–47

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Walty H (1969) Tavole Svizzere di funghi, vol. III, 3rd edn. tav. 39

  • Wanasinghe DN, Jones EBG, Camporesi E, Boonmee S, Ariyawansa HA, Wijayawardene NN, Hyde KD (2014) An exciting novel member of Lentitheciaceae in Italy from Clematis vitalba. Cryptogam Mycol 35:323–337

    Article  Google Scholar 

  • Wanasinghe DN, Jones EBG, Camporesi E, Dissanayake AJ, Kamolhan S, Mortimer PE, Xu J, Abd-Elsalam KA, Hyde KD (2016) Taxonomy and phylogeny of Laburnicola gen. nov. and Paramassariosphaeria gen. nov. (Didymosphaeriaceae, Massarineae, Pleosporales). Fungal Biol 120(11):1354–1373

  • Wang L, Zhuang WY (2004) Designing primer sets for amplification of partial calmodulin genes from penicillia. Mycosystema 23(4):466–473

    CAS  Google Scholar 

  • Wang XH, Yang ZL, Li YC, Knudsen H, Liu PG (2009) Russula griseocarnosa sp. nov. (Russulaceae, Russulales), a commercially important edible mushroom in tropical China: mycorrhiza, phylogenetic position, and taxonomy. Nova Hedwigia 88:269–282

    Article  Google Scholar 

  • Wang Y, Hyde KD, McKenzie EHC, Jiang YL, Li DW, Zhao DG (2015) Overview of Stachybotrys (Memnoniella) and current species status. Fungal Divers 71:17–83

    Article  Google Scholar 

  • Wannathes N, Desjardin DE, Hyde KD, Perry BA, Lumyong S (2009) A monograph of Marasmius (Basidiomycota) from Northern Thailand based on morphological and molecular (ITS sequences) data. Fungal Divers 37:209–306

    Google Scholar 

  • Wartchow F (2012) Clavulina incrustata, a new species from Pernambuco, Brazil. Cryptogam Mycol 33(1):105–113

    Article  Google Scholar 

  • Watanabe T (1994) Two new species of homothallic Mucor in Japan. Mycologia 86:691–695

    Article  Google Scholar 

  • Watanabe T, Shitan N, Suzuki S, Umezawa T, Shimada M, Yazaki K, Hattori T (2010) Oxalate efflux transporter from the brown rot fungus Fomitopsis palustris. Appl Environ Microbiol 76:7683–7690

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Weber NS (1972) The genus Helvella in Michigan. Mich Bot 11:147–201

    Google Scholar 

  • Weinstein RN, Pfister DH, Iturriaga T (2002) A phylogenetic study of the genus Cookeina. Mycologia 94(4):673–682

    Article  CAS  PubMed  Google Scholar 

  • Wen YM, Rajendran RK, Lin YF, Kirschner R, Hu S (2015) Onychomycosis associated with Exophiala oligosperma in Taiwan. Mycopathologia 181(1):83–88

    PubMed  Google Scholar 

  • White JF Jr, Bacon CW, Hywel-Jones NL, Spatafora JW (2003) Clavicipitalean fungi: evolutionary biology, chemistry, biocontrol and cultural impacts. CRC Press, Boca Raton

    Book  Google Scholar 

  • White TJ, Bruns T, Lee S, Taylor J (1990) Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ (eds) PCR protocols: a guide to methods and applications. Academic Press, San Diego, pp 315–322

    Google Scholar 

  • Wijayawardene NN, Mckenzie EHC, Hyde KD (2012) Towards incorporating anamorphic fungi in a natural classification-checklist and notes for 2011. Mycosphere 3(2):157–228

    Article  Google Scholar 

  • Wijayawardene NN, Crous PW, Kirk PM, Hawksworth DL, Boonmee S, Braun U, Dai DQ, Dsouza MJ, Diederich P, Dissanayake A, Doilom M, Hongsanan S, Jones EBG, Groenewald JZ, Jayawardena R, Lawrey JD, Liu JK, Lücking R, Madrid H, Manamgoda DS, Muggia L, Nelsen MP, Phookamsak R, Suetrong S, Tanaka K, Thambugala KM, Wanasinghe DN, Wikee S, Zhang Y, Aptroot A, Ariyawansa HA, Bahkali AH, Bhat DJ, Gueidan C, Chomnunti P, De Hoog GS, Knudsen K, Li WJ, McKenzie EHC, Miller AN, Phillips AJL, Piątek M, Raja HA, Shivas RS, Slippers B, Taylor JE, Tian Q, Wang Y, Woudenberg JHC, Cai L, Jaklitsch WM, Hyde KD (2014a) Naming and outline of Dothideomycetes-2014 including proposals for the protection or suppression of generic names. Fungal Divers 69:1–55

    Article  PubMed  PubMed Central  Google Scholar 

  • Wijayawardene NN, Hyde KD, Bhat DJ, Camporesi E, Schumacher RK, Chethana KWT, Wikee S, Bahkali AH, Wang Y (2014b) Camarosporium-like species are polyphyletic in Pleosporales; introducing Paracamarosporium and Pseudocamarosporium gen. nov. in Montagnulaceae. Cryptogam Mycol 35:177–198

    Article  Google Scholar 

  • Wijayawardene NN, Bhat DJ, Hyde KD, Camporesi E, Chethana KWT, Tangthirasunun N, Wang Y (2014c) Camarosporium sensu stricto in Pleosporineae, Pleosporales with two new species. Phytotaxa 183(1):16–26

    Article  Google Scholar 

  • Wijayawardene NN, Hyde KD, Bhat DJ, Goonasekars ID, Nadeeshan D, Camporesi E, Schumacher RK, Wang Y (2015) Additions to brown spored coelomycetous taxa in Massarinae, Pleosporales: introducing Phragmocamarosporium gen. nov. and Suttonomyces gen. nov. Cryptogam Mycol 36:213–224

    Article  Google Scholar 

  • Wijayawardene NN, Hyde KD, Wanasinghe DN, Papizadeh M, Goonasekara ID, Camporesi E, Bhat DJ, McKenzie EHC, Phillips AJL, Diederich P, Tanaka K, Li WJ, Tangthirasunun N, Phookamsak R, Dai DQ, Dissanayake AJ, Weerakoon G, Maharachchikumbura SSN, Hashimoto A, Matsumura M, Bahkali AH, Wang Y (2016) Taxonomy and phylogeny of dematiaceous coelomycetes. Fungal Divers 77:1–316

    Article  Google Scholar 

  • Wikee S, Lombard L, Nakashima C, Motohashi K, Chukeatirote E, Cheewangkoon R, McKenzie EHC, Hyde KD, Crous PW (2013) A phylogenetic re-evaluation of Phyllosticta (Botryosphaeriales). Stud Mycol 76:1–29

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Winter G (1885) Pilze—Ascomyceten. In: GL Rabenhorst’s Kryptogamen-Flora von Deutschland, Oesterreich und der Schweiz 1:65–528

  • Winter G (1886) Rabenhorst’s Kryptogamen-Flora, Pilze—Ascomyceten 1(2):570

  • Wolf FA (1935) Morphology of Polythrincium, causing sooty blotch of clover. Mycologia 27(1):58–73

    Article  Google Scholar 

  • Wolfe CB (1979) Austroboletus and Tylopilus subgenus Porphyrellus with emphasis on North American taxa. Bibl Mycol 69:1–132

    CAS  Google Scholar 

  • Wolfe BE, Kuo M, Pringle A (2012a) Amanita thiersii is a saprotrophic fungus expanding itsrange in the United States. Mycologia 104:22–23

    Article  CAS  PubMed  Google Scholar 

  • Wolfe BE, Tulloss RE, Pringle A (2012b) The irreversible loss of a decomposition pathway marks the single origin of an ectomycorrhizal symbiosis. PLoS ONE 7(7):539–597

    Article  CAS  Google Scholar 

  • Woo PC, Ngan AH, Tsang CC, Ling IW, Chan JF, Leung SY, Yuen KY, Lau SK (2013) Clinical spectrum of Exophiala infections and a novel Exophiala species, Exophiala hongkongensis. J Clin Microbiol 51(1):260–267

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Woronichin NN (1925) Über die Capnodiales. Ann Mycol 23:174–178

    Google Scholar 

  • Woudenberg JHC, Aveskamp MM, De Gruyter J, Spiers AG, Crous PW (2009) Multiple Didymella teleomorphs are linked to the Phoma clematidina morphotype. Persoonia 22(1):56–62

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Wu G, Feng B, Xu J, Zhu XT, Li YC, Zeng NK, Hosen IMD, Yang ZL (2014) Molecular phylogenetic analyses redefine seven major clades and reveal 22 new generic clades in the fungal family Boletaceae. Fungal Divers 69:93–115

    Article  Google Scholar 

  • Wyka SA, Broders KD (2016) The new family Septorioideaceae, within the Botryosphaeriales and Septorioides strobi as a new species associated with needle defoliation of Pinus strobus in the United States. Fungal Biol 120(8):1030–1040

    Article  PubMed  Google Scholar 

  • Yang T, Groenewald JZ, Cheewangkoon R, Jami F, Abdollahzadeh J, Lombard L, Crous PW (2017) Families, genera and species of Botryosphaeriales. Fungal Biol. doi:10.1016/j.funbio.2016.11.001

    Google Scholar 

  • Yang YL, Liu ZY, Cai L, Hyde KD, Yu ZN, McKenzie EHC (2009) Colletotrichum anthracnose of Amaryllidaceae. Fungal Divers 39:123–146

    Google Scholar 

  • Yang ZL (1997) Die Amanita-Arten von Südwestchina. Bibl Mycol 170:1–240

    Google Scholar 

  • Yang ZL (1990) Several noteworthy higher fungi from southern Yunnan, China. Mycotaxon 38:407–416

    Google Scholar 

  • Yang ZL (2000) Species diversity of the genus Amanita (Basidiomycetes) in China. Acta Bot Yunnan 22:135–142

    Google Scholar 

  • Yip HY (1988) Berkleasmium correae sp. novo on leaf hairs of Correa lawrenciana. Australas Plant Pathol 17:31–33

    Article  Google Scholar 

  • Yuan HS, Dai YC (2008) Polypores from northern and central Yunnan Province, Southwestern China. Sydowia 60:147–159

    Google Scholar 

  • Zeng JS, Feng PY, Gerrits van denEnde AHG, Xi LY, Harrak MJ, de Hoog GS (2014) Multilocus analysis of the Exophiala jeanselmei clade containing black yeasts involved in opportunistic disease in humans. Fungal Divers 65:3–16

  • Zhang LF, Yang JB, Yang ZL (2004) Molecular phylogeny of eastern Asian species of Amanita (Agaricales, Basidiomycota): taxonomic and biogeography implications. Fungal Divers 17:219–238

    Google Scholar 

  • Zhang N, Castlebury LA, Miller AN, Huhndorf SM, Schoch CL, Seifert KA, Rossman AY, Rogers JD, Kohlmeyer J, Volkmann-Kohlmeyer B, Sung GH (2006) An overview of the systematics of the Sordariomycetes based on four-gene phylogeny. Mycologia 98:1076–1087

    Article  CAS  PubMed  Google Scholar 

  • Zhang Y, Schoch CL, Fournier J, Crous PW, De Gruyter J, Woudenberg JHC, Hirayama K, Tanaka K, Pointing SB, Spatafora JW, Hyde KD (2009a) Multi-locus phylogeny of the Pleosporales: a taxonomic, ecological and evolutionary re-evaluation. Stud Mycol 64:85–102

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zhang Y, Wang HK, Fournier J, Crous PW, Jeewon R, Pointing SB, Hyde KD (2009b) Towards a phylogenetic clarification of Lophiostoma/Massarina and morphologically similar genera in the Pleosporales. Fungal Divers 38:25–51

    Google Scholar 

  • Zhang Y, Fournier J, Bahkar AH, Hyde KD (2011) Inflatispora, a novel lignicolous genus of Pleosporales from France. Sydowia 62:287–295

    Google Scholar 

  • Zhang XY, Bao J, Wang GH, He F, Xu XY, Qi SH (2012a) Diversity and antimicrobial activity of culturable fungi isolated from six species of the South China Sea gorgonians. Microb Ecol 64:617–627

    Article  CAS  PubMed  Google Scholar 

  • Zhang Y, Crous PW, Schoch CL, Hyde KD (2012b) Pleosporales. Fungal Divers 53(1):1–221

    Article  CAS  PubMed  Google Scholar 

  • Zhang H, Hyde KD, Zhao Y, McKenzie EH, Zhou D (2014) Freshwater ascomycetes: Lophiostoma vaginatispora comb. nov. (Dothideomycetes, Pleosporales, Lophiostomaceae) based on morphological and molecular data. Phytotaxa 176:184–191

    Article  Google Scholar 

  • Zhang M, He W, Wu JR, Zhang Y (2017) Two new species of Spencermartinsia (Botryosphaeriaceae, Botryosphaeriales) from China. Mycosphere 7(7):942–949

    Google Scholar 

  • Zhao K, Wu G, Jang L (2014) A new genus, Rubroboletus, to accommodate B. sinicus and its allies. Phytotaxa 188(2):61–77

    Article  Google Scholar 

  • Zhao Q, Tolgor B, Zhao YC, Yang ZL, Hyde KD (2015) Species diversity within the Helvella crispa group (Ascomycota: Helvellaceae) in China. Phytotaxa 239:130–142

    Article  Google Scholar 

  • Zhao Q, Sulayman M, Zhu XT, Zhao YC, Yang ZL, Hyde KD (2016a) Species clarification of the culinary Bachu mushroom in Western China. Mycologia 108(4):828–836

    Article  PubMed  Google Scholar 

  • Zhao Q, Zhang XL, Li SH, Chai HM, Bahkali AH, Hyde KD (2016b) New species and records of saddle fungi (Helvella, Helvellaceae) from Jiuzhaigou Natural Reserve, China. Mycoscience 57(6):422–430

    Article  Google Scholar 

  • Zhao Q, Brooks S, Zhao YC, Yang ZL, Hyde KD (2016c) Morphology and phylogenetic position of Wynnella subalpina sp. nov. (Helvellaceae) from western China. Phytotaxa 270(1):41–48

    Article  Google Scholar 

  • Zhaxybayeva O, Gogarten JP (2002) Bootstrap, Bayesian probability and maximum likelihood mapping: exploring new tools for comparative genome analyses. BMC Genom 3(1):4

    Article  Google Scholar 

  • Zhou LW, Wei YL (2011) Changbai wood-rooting fungi 16. A new species of Fomitopsis (Fomitopsidaceae). Mycol Prog 11:435–441

    Article  Google Scholar 

  • Zobel (1854) Icones fungorum hucusque cognitorum 6:4

  • Zogg H (1962) Die Hysteriaceae s. str. und Lophiaceae. Beiträge zur Kryptogamenflora der Schweiz 11(3):1–190

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Acknowledgements

Saowaluck Tibpromma would like to thank the Molecular Biology Experimental Center at Kunming Institute of Botany for facilities for molecular work, the Mushroom Research Foundation (MRF), Chiang Rai, Thailand for the financial support of her study and Shaun Pennycook is thanked for nomenclatural advice. K.D. Hyde would like to thank the Thailand Research Fund Grant No. RSA5980068 entitled “Biodiversity, phylogeny and role of fungal endophytes on above parts of Rhizophora apiculata and Nypa fruticans”, the Chinese Academy of Sciences, Project Number 2013T2S0030, for the award of Visiting Professorship for Senior International Scientists at Kunming Institute of Botany and National Research Council of Thailand (Mae Fah Luang University) for a grants “Biodiversity, phylogeny and role of fungal endophytes of Pandanaceae” (Grant No.: 592010200112), “Diseases of mangrove trees and maintenance of good forestry practice” (Grant No.: 60201000201) for supporting this study. S.C. Karunarathna, P.E. Mortimer and J.C. Xu would like to thank the World Agroforestry Centre, East and Central Asia Office; Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science; the Chinese; Ministry of Science and Technology, under the 12th 5-year National Key Technology Support Program (NKTSP)2013 BAB07B06 integration and comprehensive demonstration of key technologies on Green Phosphate-mountaion Construction and the CGIAR Research Program 6: Forest, Trees and Agroforestry for partial funding. The authors would like to extend their sincere appreciation to the Deanship of Scientific Research at King Saud University for funding this research group NO (RG-1436-025). Financial support by the German Academic Exchange Service (DAAD) and the Thai Royal Golden Ph.D. Jubilee-Industry program (RGJ) for a joint TRF-DAAD PPP (2012–2014) academic exchange grant to K.D. Hyde and M. Stadler, and the RGJ for a personal grant to B. Thongbai (No. Ph.D/0138/2553 in 4.S.MF/53/A.3) is gratefully acknowledged. Chayanard Phukhamsakda (PHD/0020/2557) acknowledges the Royal Golden Jubilee Ph.D. Program under the Thailand Research Fund. Mingkwan Doilom acknowledges the Royal Golden Jubilee Ph.D. Program (PHD./0072/2553 in 4.S.M.F./53/A.2) under the Thailand Research Fund. Ausana Mapook is grateful to Research and Researchers for Industries (RRI) PHD57I0012. Rungtiwa Phookamsak expresses sincere appreciation to The CAS President’s International Fellowship for Postdoctoral Researchers (Project No. 2017PB0072). Qi Zhao thanks the National Natural Science Foundation of China (No. 31360015) and the CAS/SAFEA International Partnership Program for Creative Research Teams, and the Knowledge Innovation Program of the Chinese Academy of Sciences (No. KSCX2-EW-Z-9 and KIB2016002). André Luiz Cabral Monteiro de Azevedo Santiago, Carlos Alberto Fragoso de Souza, Diogo Xavier Lima, Rafael José Vilela de Oliveira and Gladstone Alves da Silva would like to thank the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Coordination for the Improvement of Higher Education Personnel) (CAPES) and the Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco (Foundation for the support of Science and Technology of the state of Pernambuco) (FACEPE) for the postgraduate scholarships awarded to Diogo X. Lima and Carlos A. F. de Souza, respectively. We would also like to thank the Conselho Nacional de Desenvolvimento Científico e Tecnológico (National Council for Scientific and Technological Development) (CNPq) and FACEPE for financial support through the projects: ‘Mucoromycotina in upland forests in the semi-arid region of Pernambuco’ (CNPq-458391/2014-0), and ‘Diversity of Mucoromycotina in different ecosystems of the Pernambuco Atlantic Rainforest’ (FACEPE—APQ 0842-2.12/14). H.B. Lee was supported by the Graduate Program for the Undiscovered Taxa of Korea, and by the Project on Survey and Discovery of Indigenous Fungal Species of Korea funded by NIBR and Project on Discovery of Fungi from Freshwater and Collection of Fungarium funded by NNIBR of the Ministry of Environment (MOE), and in part by a fund from National Institute of Animal Science under Rural Development Administration, Republic of Korea. Z.L Luo and H.Y Su would like to thank the National Natural Science Foundation of China (Project ID: 31460015) for financial support on Study of the distribution pattern and driving factors of aquatic fungal diversity in the region of Three Parallel Rivers. Saranyaphat Boonmee thanks the National Research Council of Thailand, project number 2560A30702021 and the Thailand Research Fund, project number TRG5880152 for providing financial support. C.G. Lin and Y. Wang thank the grant from the National Natural Science Foundation of China (No. NSFC 31560489) and Fundamental Research on Science and Technology, Ministry of Science and Technology of China (2014FY120100) and Mr. Jingzu Sun thank for the National Natural Science Foundations of China (No. 31600024). Wei Dong thanks the for National Natural Science Foundation of China (Project ID: NSF 31500017 to Huang Zhang). P.N. Singh, A. Baghela, S.K. Singh, and S. Aamir thank the Director, MACS’ Agharkar Research Institute, Pune, India for providing facilities and Rajendra Singh (Department of Zoology, DDU Gorakhpur University, UP, India) for identification of insect-host. Saisamorn Lumyong and Rene K. Schumacher are thanked for valuable suggestions and collecting specimens. K.N.A. Raj acknowledges support from the University Grants Commission (UGC), India, in the form of a Rajiv Gandhi National Fellowship (Grant No. F.14-2(SC)/2009 (SA-III)). K.N.A. Raj also acknowledges the permissions given to him for collecting agaric specimens from the forests of Kerala by the Principal Chief Conservator of Forests, Government of Kerala (WL12-4042/2009 dated 5 August 2009). K.P.D. Latha acknowledges the financial support from the Kerala State Council for Science, Technology and Environment (KSCSTE) in the form of a PhD fellowship (Grant No. 001/FSHP/2011/CSTE). K.P.D. Latha also acknowledges the permission (No. WL10-4937/2012, dated 3-10-2013) given to her by the Principal Chief Conservator of Forests, Government of Kerala, to collect agaric specimens from the forests of Kerala. Zdenko Tkalčec has been partially supported by Croatian Science Foundation under the project HRZZ-IP-11-2013-2202 (ACCTA) and is grateful to Milan Čerkez for his great contribution to the study of coprinoid and coprophilous fungi in Croatia. Vladimir Antonín thank the Moravian Museum by the Ministry of Culture of the Czech Republic as part of its long-term conceptual development programme for research institutions (DKRVO, ref. MK000094862). T.C. Wen, Y.P. Xiao, C. Norphanphoun and K.K. Hapuarachchi are grateful to the National Natural Science Foundation of China (No. 31460012) and the Science and Technology Foundation of Guizhou Province (No. [2016]2863). Y.W. Lim would like to thanks NIBR supporting the Project on Survey and Discovery of Indigenous Fungal Species of Korea. Kanad Das and Dyutiparna Chakraborty are thankful to the Director, Botanical Survey of India (BSI) and Scientist-in-Charge, BSI, Gangtok for providing facilities during this study. Sinchan Adhikari, Joydeep Karmakar and Tapas Kumar Bandyopadhyay would like to acknowledge DST-PURSE and DST-FIST for providing central instrumentation facilities and Alan JL Phillips acknowledges the Biosystems and Integrative Sciences Institute (BioISI, FCT/UID/Multi/04046/2013).

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Authors and Affiliations

  1. Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming, 650201, Yunnan, People’s Republic of China

    Saowaluck Tibpromma, Kevin D. Hyde, Rungtiwa Phookamsak, Chayanard Phukhamsakda, Dhanushka N. Wanasinghe, Indunil C. Senanayake, Ishani D. Goonasekara, N. I. de Silva, Sehroon Khan, Wen-Jing Li, Jianchu Xu, Peter E. Mortimer & Samantha C. Karunarathna

  2. Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand

    Saowaluck Tibpromma, Kevin D. Hyde, Mingkwan Doilom, Anusha Hasini Ekanayaka, Benjarong Thongbai, Saranyaphat Boonmee, Rungtiwa Phookamsak, Chayanard Phukhamsakda, Sirinapa Konta, Subashini C. Jayasiri, Chada Norphanphoun, Danushka S. Tennakoon, Junfu Li, Monika C. Dayarathne, Rekhani H. Perera, Yuanpin Xiao, Dhanushka N. Wanasinghe, Indunil C. Senanayake, Ishani D. Goonasekara, N. I. de Silva, Ausana Mapook, Ruvishika S. Jayawardena, Asha J. Dissanayake, Ishara S. Manawasinghe, K. W. Thilini Chethana, Zong-Long Luo, Kalani Kanchana Hapuarachchi, Chuan-Gen Lin, Dinushani A. Daranagama, Jingzu Sun, Kasun M. Thambugala, Milan C. Samarakoon, Nalin N. Wijayawardene, Qing Tian, Sinang Hongsanan, Wen-Jing Li & Putarak Chomnunti

  3. School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand

    Saowaluck Tibpromma, Kevin D. Hyde, Chayanard Phukhamsakda, Sirinapa Konta, Subashini C. Jayasiri, Chada Norphanphoun, Danushka S. Tennakoon, Junfu Li, Monika C. Dayarathne, Rekhani H. Perera, Yuanpin Xiao, Dhanushka N. Wanasinghe, Indunil C. Senanayake, Ishani D. Goonasekara, Ausana Mapook, Kalani Kanchana Hapuarachchi, Chuan-Gen Lin, Dinushani A. Daranagama, Jingzu Sun, Kasun M. Thambugala, Qing Tian, Wen-Jing Li, Putarak Chomnunti & Sureeporn Nontachaiyapoom

  4. World Agroforestry Centre, East and Central Asia, Kunming, 650201, Yunnan, People’s Republic of China

    Saowaluck Tibpromma, Kevin D. Hyde, Rungtiwa Phookamsak, Chayanard Phukhamsakda, Dhanushka N. Wanasinghe, Indunil C. Senanayake, Ishani D. Goonasekara, N. I. de Silva, Milan C. Samarakoon, Sehroon Khan, Jianchu Xu, Peter E. Mortimer & Samantha C. Karunarathna

  5. Mushroom Research Foundation, 128 M.3 Ban Pa Deng T. Pa Pae, A. Mae Taeng, Chiang Mai, 50150, Thailand

    Saowaluck Tibpromma, Kevin D. Hyde, Sirinapa Konta, Subashini C. Jayasiri, Chada Norphanphoun, Danushka S. Tennakoon, Junfu Li, Monika C. Dayarathne, Rekhani H. Perera, Yuanpin Xiao, Dhanushka N. Wanasinghe, Indunil C. Senanayake, Ishani D. Goonasekara, Chuan-Gen Lin, Dinushani A. Daranagama, Kasun M. Thambugala, Milan C. Samarakoon, Qing Tian & Wen-Jing Li

  6. A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy

    Erio Camporesi

  7. A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314, Brescia, Italy

    Erio Camporesi

  8. Società per gli Studi Naturalistici della Romagna, C.P. 144, Bagnacavallo, RA, Italy

    Erio Camporesi

  9. Formerly Department of Botany, Goa University, Taleigão, Goa, India

    D. Jayarama Bhat

  10. No. 128/1-J, Azad Housing Society, Curca, Goa Velha, India

    D. Jayarama Bhat

  11. 33 B St. Edwards Road Southsea Hants, Hampshire, PO5 3DH, UK

    E. B. Gareth Jones

  12. Landcare Research Manaaki Whenua, Private Bag 92170, Auckland, New Zealand

    Eric H. C. McKenzie

  13. Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai, 50200, Thailand

    N. I. de Silva, Milan C. Samarakoon & Itthayakorn Promputtha

  14. Division of Applied Science, College of International Education, The Hong Kong Baptist University, Hong Kong SAR, China

    Alvin M. C. Tang

  15. PostGraduate Program in Biology of Fungi, Department of Mycology, Federal University of Pernambuco, Av. Nelson Chaves, s/n, Recife, PE, 50670-420, Brazil

    André Luiz Cabral Monteiro de Azevedo Santiago, Carlos Alberto Fragoso de Souza, Diogo Xavier Lima, Gladstone Alves da Silva & Rafael José Vilela de Oliveira

  16. Institute of Plant and Environment Protection, Beijing Academy of Agriculture and Forestry Sciences, Beijing, 100097, People’s Republic of China

    Ruvishika S. Jayawardena, Asha J. Dissanayake, Ishara S. Manawasinghe, K. W. Thilini Chethana & Jiye Yan

  17. Environmental Microbiology Lab, Division of Food Technology, Biotechnology & Agrochemistry, College of Agriculture and Life Sciences, Chonnam National University, Yongbong-Dong 300, Buk-Gu, Gwangju, 61186, Korea

    Hyang Burm Lee & Thi Thuong Thuong Nguyen

  18. Guizhou Key Laboratory of Agricultural Biotechnology, Guizhou Academy of Agricultural Sciences, Guiyang, 550006, Guizhou, People’s Republic of China

    Jian-Kui Liu & Kasun M. Thambugala

  19. College of Agriculture and Biological Sciences, Dali University, Dali, 671003, Yunnan, People’s Republic of China

    Zong-Long Luo & Hong-Yan Su

  20. Yunnan Institute of Food Safety, Kunming University of Science & Technology, Kunming, 650500, Yunnan, People’s Republic of China

    Wei Dong & Huang Zhang

  21. State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences (IMCAS), No. 3 Park 1, West Beichen Road, Chaoyang District, Beijing, 100101, People’s Republic of China

    Jingzu Sun

  22. National Fungal Culture Collection of India, Biodiversity and Palaeobiology Group, MACS Agharkar Research Institute, G.G. Agarkar Road, Pune, 411 004, India

    Sanjay K. Singh, Abhishek Baghela, Kunhiraman C. Rajeshkumar, Paras Nath Singh, S. Aamir & Sayali D. Marathe

  23. Institute for Sustainable Plant Protection (IPSP)‐CNR, Viale P.A. Mattioli 25, 10125, Turin, Italy

    Alfredo Vizzini

  24. Faculty of Agriculture, Princess of Naradhiwas University, No. 99 Khok Khian, Amphur Muang, Narathiwat Province, Thailand

    Saithong Kaewchai

  25. Department of Crop Sciences, College of Agricultural and Marine Sciences, Sultan Qaboos University, P.O. Box 34, 123, Al-Khod, Oman

    Sajeewa S. N. Maharachchikumbura

  26. Institute of Microbiology, Beijing Forestry University, PO Box 61, Beijing, 100083, China

    Fang Wu & Jie Song

  27. Russian Research Institute of Floriculture and Subtropical Crops, 2/28 Yana Fabritsiusa Street, Sochi, Krasnodar region, Russia, 354002

    Timur S. Bulgakov

  28. Engineering Research Center of Southwest Bio-Pharmaceutical Resources, Ministry of Education, Guizhou University, Guiyang, 550025, Guizhou, People’s Republic of China

    Kalani Kanchana Hapuarachchi, Kang Ji-Chuan & Ting-Chi Wen

  29. Department of Health Sciences, Faculty of Science, University of Mauritius, Reduit, 80837, Mauritius

    Rajesh Jeewon

  30. School of Biological Sciences, Seoul National University, Seoul, 08826, Korea

    Young Woon Lim, Hyun Lee & Nam Kyu Kim

  31. Molecular and Applied Mycology and Plant Pathology Laboratory, Department of Botany, University of Calcutta, Kolkata, West Bengal, 700019, India

    Arun Kumar Dutta & Krishnendu Acharya

  32. Moravian Museum, Department of Botany, Zelný trh 6, 659 37, Brno, Czech Republic

    Vladimír Antonín

  33. Department of Botany, University of Calicut, Malappuram, Kerala, 673 635, India

    Patinjareveettil Manimohan, K. N. Anil Raj & K. P. Deepna Latha

  34. Botanical Survey of India, Cryptogamic Unit, P.O. Botanic Garden, Howrah, 711103, India

    Kanad Das & Dyutiparna Chakraborty

  35. Department of Botany, University of Kalyani, Kalyani, Nadia, West Bengal, 741235, India

    Sinchan Adhikari

  36. Department of Molecular Biology & Biotechnology, University of Kalyani, Kalyani, Nadia, West Bengal, 741235, India

    Joydeep Karmakar & Tapas Kumar Bandyopadhyay

  37. Laboratorio di Isto-Cito-Patologia s.n.c., Via del Bosco, 96, 95125, Catania, Italy

    Gianrico Vasquez

  38. Via Bell’Aria, 8, 42121, Reggio nell’Emilia (RE), Italy

    Giampaolo Simonini

  39. Biology and Technologies of Living Systems Department, Tula State Lev Tolstoy Pedagogical University, 125, Lenin av., Tula, Russia, 300026

    Tatyana Yu. Svetasheva

  40. Department of Life Sciences and Systems Biology, University of Turin, Viale P.A. Mattioli, 25, 10125, Turin (TO), Italy

    Alfredo Vizzini & Enrico Ercole

  41. Lečkova 1521/15, 14900, Prague 4, Czech Republic

    Michal Mikšík

  42. Universidade Federal de Pernambuco (UFPE), Centro de Biociências (CB), Departamento de Micologia, Avenida da Engenharia, S/N - Cidade Universitária, Recife, PE, 50740-600, Brazil

    Tatiana B. Gibertoni, Adriene Mayra Soares & Angelina Meiras-Ottoni

  43. University of Lisbon, Faculty of Sciences, Biosystems and Integrative Sciences Institute (BioISI), Campo Grande, 1749-016, Lisbon, Portugal

    Alan J. L. Phillips

  44. Instituto de Ciências Biológicas, Laboratório de Microbiologia, Av. Augusto Corrêa, Belém, Pará, 66075-110, Brazil

    Helio Longoni Plautz Jr.

  45. Department of Botany, University of Oslo, Blindern, P. O. Box 1045, 0316, Oslo, Norway

    Leif Ryvarden

  46. Ruđer Bošković Institute, Bijenička cesta 54, 10000, Zagreb, Croatia

    Armin Mešić, Ivana Kušan, Margita Jadan, Neven Matočec & Zdenko Tkalčec

  47. Department of Biology, College of Sciences, Eritrea Institute of Technology, P. Box 12676, Mai Nafhi, Asmara, Eritrea

    Kamal C. Semwal

  48. Genetics and Molecular Biology Division, CSIR-National Botanical Research Institute, Lucknow, 226001, Uttar Pradesh, India

    Debasis Chakrabarty & Yuvraj Indoliya

  49. Department of Botany & Microbiology, H.N.B. Garhwal University, Srinagar, Garhwal, 246174, Uttarakhand, India

    R. P. Bhatt & Tahir Mehmood

  50. P. O. Box 57, Roosevelt, NJ, 08555-0057, USA

    Rodham E. Tulloss

  51. State Key Laboratory of Applied Microbiology Southern China, Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangdong Institute of Microbiology, Guangzhou, 510070, People’s Republic of China

    Md. Iqbal Hosen

  52. Key Lab of Southwestern Crop Gene Resources and Germplasm Innovation Ministry of Agriculture, Yunnan Provincial Key Laboratory of Agricultural Biotechnology, Institute of Biotechnology and Germplasm Resources, Yunnan Academy of Agricultural Sciences, Kunming, 650223, Yunnan, People’s Republic of China

    Qi Zhao

  53. Ecology Division, Biotechnology and Ecology Institute, Ministry of Science and Technology, P.O.Box: 2279, Vientiane Capital, Lao People’s Democratic Republic

    Phongeun Sysouphanthong

  54. State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming, People’s Republic of China

    Kaifeng Hu

  55. Germplasm Bank of Wild Species in Southwest China, Kunming Institute of Botany, Chinese Academy of Science, Kunming, 650201, Yunnan, People’s Republic of China

    Jun-Bo Yang

  56. Microbe Interaction Laboratory (BMIT), BIOTEC, National Science and Technology Development Agency (NSTDA), 113 Thailand Science Park, Thanon Phahonyothin, Tombon Khlong Nueng, Amphoe, Khlong Luang, Pathum Thani, 12120, Thailand

    Jennifer Luangsa-ard

  57. Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box: 2455, Riyadh, 1145, Saudi Arabia

    Abdallah M. Elgorban & Ali H. Bahkali

  58. Department of Microbial Drugs, Helmholtz Centre for Infection Research and German Centre for Infection Research (DZIF), Partner Site Hannover/Braunschweig, Inhoffenstrasse 7, 38124, Braunschweig, Germany

    Christian Richter & Marc Stadler

  59. Department of Plant Pathology, College of Agriculture, Guizhou University, Guiyang, 550025, Guizhou, People’s Republic of China

    Chuan-Gen Lin, Kerstin Voigt & Yong Wang

  60. Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3DS, UK

    Paul M. Kirk

  61. Department of Plant Pathology and Microbiology, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei, 106, Taiwan, People’s Republic of China

    Hiran A. Ariyawansa

Authors
  1. Saowaluck Tibpromma
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  2. Kevin D. Hyde
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  3. Rajesh Jeewon
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Correspondence to Samantha C. Karunarathna.

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Tibpromma, S., Hyde, K.D., Jeewon, R. et al. Fungal diversity notes 491–602: taxonomic and phylogenetic contributions to fungal taxa. Fungal Diversity 83, 1–261 (2017). https://doi.org/10.1007/s13225-017-0378-0

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