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Fungal diversity notes 253–366: taxonomic and phylogenetic contributions to fungal taxa

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Abstract

Notes on 113 fungal taxa are compiled in this paper, including 11 new genera, 89 new species, one new subspecies, three new combinations and seven reference specimens. A wide geographic and taxonomic range of fungal taxa are detailed. In the Ascomycota the new genera Angustospora (Testudinaceae), Camporesia (Xylariaceae), Clematidis, Crassiparies (Pleosporales genera incertae sedis), Farasanispora, Longiostiolum (Pleosporales genera incertae sedis), Multilocularia (Parabambusicolaceae), Neophaeocryptopus (Dothideaceae), Parameliola (Pleosporales genera incertae sedis), and Towyspora (Lentitheciaceae) are introduced. Newly introduced species are Angustospora nilensis, Aniptodera aquibella, Annulohypoxylon albidiscum, Astrocystis thailandica, Camporesia sambuci, Clematidis italica, Colletotrichum menispermi, C. quinquefoliae, Comoclathris pimpinellae, Crassiparies quadrisporus, Cytospora salicicola, Diatrype thailandica, Dothiorella rhamni, Durotheca macrostroma, Farasanispora avicenniae, Halorosellinia rhizophorae, Humicola koreana, Hypoxylon lilloi, Kirschsteiniothelia tectonae, Lindgomyces okinawaensis, Longiostiolum tectonae, Lophiostoma pseudoarmatisporum, Moelleriella phukhiaoensis, M. pongdueatensis, Mucoharknessia anthoxanthi, Multilocularia bambusae, Multiseptospora thysanolaenae, Neophaeocryptopus cytisi, Ocellularia arachchigei, O. ratnapurensis, Ochronectria thailandica, Ophiocordyceps karstii, Parameliola acaciae, P. dimocarpi, Parastagonospora cumpignensis, Pseudodidymosphaeria phlei, Polyplosphaeria thailandica, Pseudolachnella brevifusiformis, Psiloglonium macrosporum, Rhabdodiscus albodenticulatus, Rosellinia chiangmaiensis, Saccothecium rubi, Seimatosporium pseudocornii, S. pseudorosae, Sigarispora ononidis and Towyspora aestuari. New combinations are provided for Eutiarosporella dactylidis (sexual morph described and illustrated) and Pseudocamarosporium pini. Descriptions, illustrations and / or reference specimens are designated for Aposphaeria corallinolutea, Cryptovalsa ampelina, Dothiorella vidmadera, Ophiocordyceps formosana, Petrakia echinata, Phragmoporthe conformis and Pseudocamarosporium pini. The new species of Basidiomycota are Agaricus coccyginus, A. luteofibrillosus, Amanita atrobrunnea, A. digitosa, A. gleocystidiosa, A. pyriformis, A. strobilipes, Bondarzewia tibetica, Cortinarius albosericeus, C. badioflavidus, C. dentigratus, C. duboisensis, C. fragrantissimus, C. roseobasilis, C. vinaceobrunneus, C. vinaceogrisescens, C. wahkiacus, Cyanoboletus hymenoglutinosus, Fomitiporia atlantica, F. subtilissima, Ganoderma wuzhishanensis, Inonotus shoreicola, Lactifluus armeniacus, L. ramipilosus, Leccinum indoaurantiacum, Musumecia alpina, M. sardoa, Russula amethystina subp. tengii and R. wangii are introduced. Descriptions, illustrations, notes and / or reference specimens are designated for Clarkeinda trachodes, Dentocorticium ussuricum, Galzinia longibasidia, Lentinus stuppeus and Leptocorticium tenellum. The other new genera, species new combinations are Anaeromyces robustus, Neocallimastix californiae and Piromyces finnis from Neocallimastigomycota, Phytophthora estuarina, P. rhizophorae, Salispina, S. intermedia, S. lobata and S. spinosa from Oomycota, and Absidia stercoraria, Gongronella orasabula, Mortierella calciphila, Mucor caatinguensis, M. koreanus, M. merdicola and Rhizopus koreanus in Zygomycota.

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References

  • Abdel-Wahab MA, Jones EBG (2000) Three new marine ascomycetes from driftwood in Australian sand dunes. Mycoscience 41:379–388

    Article  Google Scholar 

  • Abdel-Wahab MA, Hodhod MS, Bahkali AHA, Jones EBG (2014) Marine fungi of Saudi Arabia. Bot Mar 57:323–335

    Article  Google Scholar 

  • Abe A, Oda Y, Asano Y, Sone T (2007) Rhizopus delemar is the proper name for Rhizopus oryzae fumaric-malic acid producers. Mycologia 99:714–722

    Article  CAS  PubMed  Google Scholar 

  • Abe A, Oda Y, Asano Y, Sone T (2010) A molecular phylogeny based taxonomy of the genus Rhizopus. Biosci Biotechnol Biochem 74:1325–1331

    Article  CAS  PubMed  Google Scholar 

  • Abdollahzadeh J, Javadi A, Zare R, Phillips AJL (2014) A phylogenetic study of Dothiorella and Spencermartinsia species associated with woody plants in Iran, New Zealand, Portugal and Spain. Persoonia 32:1–12

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Acero FJ, González V, Sánchez-Ballesteros J, Rubio V, Checa J, Bills GF, Salazar O, Platas G, Peláez F (2004) Molecular phylogenetic studies on the Diatrypaceae based on rDNA-ITS sequences. Mycologia 96:249–259

    Article  CAS  PubMed  Google Scholar 

  • Adams GC, Surve-Iyer RS, Iezzoni AF (2002) Ribosomal DNA sequence divergence and group I introns within the Leucostoma species L. cinctum, L. persoonii, and L. parapersoonii sp. nov., ascomycetes that cause Cytospora canker of fruit trees. Mycologia 94:947–967

    Article  CAS  PubMed  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 

  • Adl SM, Simpson AGB, Lane CE, Lukeš J, Bass D, Bowser SS, Brown MW, Burki F, Dunthorn M, Hampl V, Heiss A, Hoppenrath M, Lara E, Le Gall L, Lynn DH, McManus H, Mitchell EA, Mozley-Stanridge SE, Parfrey LW, Pawlowski J, Rueckert S, Shadwick RS, Schoch CL, Smirnov A, Spiegel FW (2012) The revised classification of Eukaryotes. J Eukaryot Microbiol 59:429–493

    Article  PubMed  PubMed Central  Google Scholar 

  • Ahmed SA, van de Sande WWJ, Stevens DA, Fahal A, van Diepeningen AD, Menken SBJ, de Hoog GS (2014) Revision of agents of black-grain eumycetoma in the order Pleosporales. Persoonia 33:141–154

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Alastruey-Izquierdo A, Hoffmann K, de Hoog GS, Rodriguez-Tudela JL, Voigt K, Bibashi E, Walther G (2010) Species recognition and clinical relevance of the zygomycetous genus Lichtheimia (syn. Absidia pro parte, Mycocladus). J Clin Microbiol 48:2154–2170

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215:403–410

    Article  CAS  PubMed  Google Scholar 

  • Álvarez E, Cano J, Stchigel AM, Sutton DA, Fothergill AW, Salas V, Rinaldi MG, Guarro J (2011) Two new species of Mucor from clinical samples. Med Mycol 49:62–72

    Article  PubMed  Google Scholar 

  • Alves MH, Campos-Takaki GM, Porto ALF, Milanez AI (2002) Screening of Mucor spp. for the production of amylase, lipase, polygalacturonase and protease. Braz J Microbiol 33:325–330

    CAS  Google Scholar 

  • Amalfi M, Yombiyeni P, Decock C (2010) Fomitiporia in sub-Saharan Africa: morphology and multi-gene phylogenetic analysis support three new species from the Guineo-Congolian rainforest. Mycologia 102:1303–1317

    Article  PubMed  Google Scholar 

  • Amalfi M, Decock C (2013) Fomitiporia castilloi sp. nov. and multiple clades around F. apiahyna and F. texana in Meso- and South America evidenced by multi-loci phylogenetic inferences. Mycologia 105:873–887

    Article  PubMed  Google Scholar 

  • Amalfi M, Raymundo T, Valenzuela R, Decock C (2012) Fomitiporia cupressicola sp. nov., a parasite on Cupressus arizonica, and additional unnamed clades in the southern USA and northern Mexico, determined by multi-locus phylogenetic analyses. Mycologia 104:880–893

    Article  PubMed  Google Scholar 

  • Amalfi M, Robledo G, Decock C (2014) Fomitiporia baccharidis comb. nov., a little known species from high elevation Andean forests and its affinities within the Fomitiporia neotropical lineages. Mycol Prog 13:995

    Article  Google Scholar 

  • Anon (1955) Shen Nong materia medica 102–200 A.D (E. Han). Reprinted. People Hygiene Press, Beijing

  • Aptroot A (1998) A world revision of Massarina (Ascomycota). Nova Hedwigia 66:89–162

    Google Scholar 

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

    Article  Google Scholar 

  • Ariyawansa HA, Phookamsak R, Tibpromma S et al. (2014b) A molecular and morphological reassessment of Diademaceae. Sci World J. Article ID 675348, 11 pages

  • Ariyawansa HA, Hawksworth DL, Hyde KD, Jones EBG, Maharachchikumbura SSN, Manamgoda DS, Thambugala KM, Udayanga D, Camporesi E, Daranagama A, Jayawardena R, Liu JK, McKenzie EHC, Phookamsak R, Senanayake IC, Shivas RG, Tian Q, Xu JC (2014b) Epitypification and neotypification: guidelines with appropriate and inappropriate examples. Fungal Divers 69:57–91

    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, Kang JC, Gareth Jones EB, Hyde KD (2015a) Towards a natural classification and backbone tree for Pleosporaceae. Fungal Divers 71:85–139

    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 ALCMDA, Sommai S, Song Y, de Souza CAF, de Souza-Motta CM, Su HY, Suetrong S, Wang Y, Fong WS, Yuan HS, 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 (2015b) Fungal diversity notes 111–252—taxonomic and phylogenetic contributions to fungal taxa. Fungal Divers 75:27–274

    Article  Google Scholar 

  • Ariyawansa HA, Phukhamsakda C, Thambugala KM, Wanasinghe DN, Perera RH, Mapook A, Camporesi E, Kang JC, Jones EBG, Bahkali AH, Bhat JD, Hyde KD (2015c) Revision and phylogeny of Leptosphaeriaceae. Fungal Divers 74:19–51

    Article  Google Scholar 

  • von Arx JA (1971) Testudinaceae, a new family of Ascomycetes. Persoonia 6:365–369

    Google Scholar 

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

    Google Scholar 

  • Balci Y, Balci S, Eggers J, MacDonald WL, Juzwik J, Long RP, Gottschalk KW (2007) Phytophthora spp. associated with forest soils in eastern and north-central US oak ecosystems. Plant Dis 91:705–710

    Article  Google Scholar 

  • Barber PA, Crous PW, Groenewald JZ, Pascoe IG, Keane P (2011) Reassessing Vermisporium (Amphisphaeriaceae), a genus of foliar pathogens of Eucalypts. Persoonia 27:90–118

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Barghoorn ES, Linder DH (1944) Marine fungi: their taxonomy andbiology. Farlowia 1:395–467

    Google Scholar 

  • Barr ME (1972) Preliminary studies on the Dothideales in temperate North America. Contrib Univ Mich Herb 9:523–638

    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 (1987) Prodomus to class Loculoascomycetes. Publ. by the author, Amherst

  • Barr ME (1989) The genus Chaetomastia (Dacampiaceae) in North America. Mycotaxon 34:507–515

    Google Scholar 

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

    Article  Google Scholar 

  • Barr ME (1979b) On the Massariaceae in North America. Mycotaxon 9:17–37

    Google Scholar 

  • Barr ME (1990) North American Flora. Melanommatales (Loculoascomycetes). New York Botanical Garden Series II Part 13:129

  • Barr ME (2001) Revisionary studies on the Dothioraceae. Harv Pap Bot 6:25–34

    Google Scholar 

  • Barr DJS, Kudo H, Jakober KD, Cheng KJ (1989) Morphology and development of rumen fungi: Neocallimastix sp., Piromyces communis, and Orpinomyces bovis gen. nov., sp. nov. Can J Bot 67:2815–2824

    Article  Google Scholar 

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

    Google Scholar 

  • Beakes GW, Honda D, Thines M (2014) Systematics of the Straminipila: Labyrinthulomycota, Hyphochytriomycota, and Oomycota. In: McLaughlin DJ, Spatafora JW (eds) The mycota VII part a––systematics and evolution. Springer-Verlag, Berlin Heidelberg, pp 39–97

    Google Scholar 

  • Benson DA, Cavanaugh M, Clark K, Karsch-Mizrachi I, Lipman DJ, Ostell J, Sayers EW (2013) GenBank. Nucleic Acids Res 41:D36–42

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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

    Google Scholar 

  • Berkeley MJ, Broome CE (1852) Notices of British fungi (615–639). Ann Mag Nat Hist 9:317–329

    Google Scholar 

  • Bernicchia A, Gorjón SP (2010) Fungi Europaei 12 - Corticiaceae s.l. Edizioni Candusso, Italy

    Google Scholar 

  • Benny GL (1995) Classical morphology in Zygomycetes taxonomy. Can J Bot 73:S725–S730

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

    Article  Google Scholar 

  • Benny GL (2013) Zygomycetes. Published on the internet at www.zygomycetes.org

  • Bessette AE, Roody WC, Bessette AR (2010) North American Boletes: a colour guide to the Fleshy Pored Mushrooms. First paperback edition. Syracuse University Press, USA, 396

  • Binder M, Hibbett DS, Wang Z, Farnham W (2006) Evolutionary relationships of Mycaureola dilseae (Agaricales), a basidiomycete pathogen of a subtidal rhodophyte. Am J Bot 93:547–556

    Article  PubMed  Google Scholar 

  • Binder M, Larsson KH, Matheny PB, Hibbett D (2010) Amylocorticiales ord. nov. and Jaapiales ord. nov.: early diverging clades of Agaricomycetidae dominated by corticioid forms. Mycologia 102:865–880

    Article  CAS  PubMed  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Blair JE, Coffey MD, Park SY, Geiser DM, Kang S (2008) A multi-locus phylogeny for Phytophthora utilizing markers derived from complete genome sequences. Fungal Genet Biol 45:266–277

    Article  CAS  PubMed  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 keys to world species. Stud Mycol 64:49–83

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Boidin J, Gilles G (1998) Contribution à l’étude des genres Dendrocorticium, Dendrodontia et Dentocorticium (Basidiomycotina). Cryptogam Mycol 19:181–202

    Google Scholar 

  • Bojantchev D (2013) Cortinarius of California: eight new species in subg. Telamonia Mycotaxon 123:375–402

    Article  Google Scholar 

  • Bojantchev D (2015) Nomenclatural novelties, Cortinarius. Index Fungorum no. 247

  • Bojantchev D, Davis RM (2011) Cortinarius xanthodryophilus sp. nov. – a common Phlegmacium under oaks in California. Mycotaxon 116:317–328

    Article  Google Scholar 

  • Boonmee S, Hyde KD, KoKo TW, Chukeatirote E, Chen H, Cai L, McKenzie EHC, Jones EBG, Kodsueb R, Hassan BA (2012) Two new Kirschsteiniotheliaceae species with Dendryphiopsis anamorphs cluster in Kirschsteiniotheliaceae fam. nov. Mycologia 104:698–714

    Article  PubMed  Google Scholar 

  • Bonorden HF (1864) Abhandlungen aus dem Gebiete der Mykologie. Abhandlungen der Naturforschenden Gesellschaft zu Halle 8:1–168

    Google Scholar 

  • Borelli D (1959) Pyrenochaeta romeroi n. sp. Dermatologia Venezplana 1:325–326

    Google Scholar 

  • Bose SK (1961) Studies on Massarina Sacc. and related genera. Phytopathol Z 41:151–213

    Article  Google Scholar 

  • Botella L, Diez JJ (2011) Phylogenic diversity of fungal endophytes in Spanish stands of Pinus halepensis. Fungal Divers 47:9–18

    Article  Google Scholar 

  • Botella L, Santamaría O, Diez JJ (2010) Fungi associated with the decline of Pinus halepensis in Spain. Fungal Divers 40:1–11

    Article  Google Scholar 

  • Brasier CM, Beales PA, Kirk SA, Denman S, Rose J (2005) Phytophthora kernoviae sp. nov., an invasive pathogen causing bleeding stem lesions on forest trees and foliar necrosis of ornamentals in the UK. Mycol Res 109:853–859

    Article  PubMed  Google Scholar 

  • Braune RA (1913) Untersuchungen über die im Wiederkäuermagen vorkommenden Protozoen. Arch Für Protistenkd 32:111–170

    Google Scholar 

  • Bresinsky A, Besl H (2003) Beiträge zu einer Mykoflora Deutschlands: Schlüssel zur Gattungsbestimmung der Blätter-, Leisten- und Röhrenpilze: mit Literaturhinweisen zur Artbestimmung. Regensburger mykologische Schriften. Verlag der Gesellschaft, Regensburg

    Google Scholar 

  • Breton A, Dusser M, Gaillard-Martine B, Guillot J, Millet L, Prensier G (1991) Piromyces rhizinflata nov. sp., a strictly anaerobic fungus from faeces of the Saharian ass: a morphological, metabolic and ultrastructural study. FEMS Microbiol Lett 82:1–8

    Article  CAS  Google Scholar 

  • Brookman JL, Mennim G, Trinci APJ, Theodorou MK, Tuckwell DS (2000) Identification and characterization of anaerobic gut fungi using molecular methodologies based on ribosomal ITS1 and 18S rRNA. Microbiology 146:393–403

    Article  CAS  PubMed  Google Scholar 

  • Budziszewska J, Piatkowska J (2010) Taxonomic position of Mucor hiemalis f. luteus. Mycotaxon 111:75–85

    Article  Google Scholar 

  • Bulgakov TS (2010) Microfungi of Leucostoma and Valsa genera and their Cytospora anamorphs on arboreal plants in the steppe zone of Southern Russia//Actual problems of ecology: Mater. IV All-Russian Scien. Conf. in Vladikavkaz, North Ossetian State University, pp 40–45. (in Russian)

  • Butin H, Holdenrieder O, Sieber TN (2013) The complete life cycle of Petrakia echinata. Mycol Prog 12:427–435

    Article  Google Scholar 

  • Buyck B (1989) Revision du genre Russula Persoon en Afrique Centrale. PhD dissertation, Rijksuniversiteit Gent

  • Buyck B, Hoyak E (1999) New taxa of pleurotoid Russulaceae. Mycologia 91:532–537

    Article  Google Scholar 

  • Buyck B, Thoen D, Watling R (1996) Ectomycorrhizal fungi of the Guinea-Congo region. Proc Royal Soc Edinburgh Sect B BioSci 104:313–333

    Google Scholar 

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

    Google Scholar 

  • Buyck B, Hofstetter V, Verbeken A, Walleyn R (2010) Proposal 1919: to conserve Lactarius nom. cons. (Basidiomycota) with a conserved type. Mycotaxon 111:504–508

    Google Scholar 

  • Cáceres MES, Aptroot A, Parnmen S, Lücking R (2014) Remarkable diversity of the lichen family Graphidaceae in the Amazon rain forest of Rondônia, Brazil. Phytotaxa 189:87–136

    Article  Google Scholar 

  • Cai L, Hyde KD, Taylor PWJ, Weir BS, Waller J, Abang MM, Zhang JZ, Yang YL, Phoulivong S, Liu ZY, Prihastuti H, Shivas RG, McKenzie EHC, Johnston PR (2009) A polyphasic approach for studying Colletotrichum. Fungal Divers 39:183–204

    Google Scholar 

  • Cai Q, Tulloss RE, Tang LP, Tolgor B, Zhang P, Chen ZH, Yang ZL (2014) Multi-locus phylogeny of lethal amanitas: implications for species diversity and historical biogeography. BMC Evol Biol 14:1–16

    Article  CAS  Google Scholar 

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

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cao Y, Wu SH, Dai YC (2012) Species clarification of the prize medicinal Ganoderma mushroom “Lingzhi”. Fungal Divers 56:49–62

    Article  Google Scholar 

  • Cao Y, Yuan HS (2013) Ganoderma mutabile sp. nov. from southwestern China based on morphological and molecular data. Mycol Progress 12:121–126

    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 

  • Ceska O (2013) The macrofungi of observatory hill: long–term survey and inventory November 2004 – March 2013. http://www.goert.ca/activities/2013/05/macrofungi–observatory–hill/

  • Chadefaud M (1960) Les végétaux non vasculaires (Cryptogamie). In: Chadefaud M, Emberger L (eds) Traité de botanique systématique, vol 1. Tome I, Masson et Cie, Paris, p 1016

  • Chaverri P, Liu M, Hodge KT (2008) A monograph of the entomopathogenic 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 

  • Chen GQ, Zheng RY (1986) A new species of Mucor with giant spores. Acta Mycol Sin 1:56–60

    Google Scholar 

  • Chen J, Zhao RL, Parra LA, Guelly AK, Kesel AD, Rapion S, Hyde KD, Chukeatirote E, Callac P (2015) Agaricus section Brunneopicti: a phylogenetic reconstruction with descriptions of four new taxa. Phytotaxa 192:145–168

    Article  Google Scholar 

  • Chen J, Zhao RL, Karunarathna SC, Callac P, Raspé O, Bahkali AH, Hyde KD (2012) Agaricus megalosporus: a new speciesin section Minores. Cryptogam Mycol 33:145–155

    Article  Google Scholar 

  • Chen JJ, Cui BK, He SH et al. (2016) Molecular phylogeny and global diversity of the remarkable genus Bondarzewia (Basidiomycota, Russulales). Mycologia. doi:10.3852/14-216

  • Chen YC, Hseu RS, Chien CY (2002) Piromyces polycephalus (Neocallimastigaceae), a new rumen fungus. Nova Hedwig 75:409–414

    Article  Google Scholar 

  • Chen ZH, Dai YD, Yu H, Yang K, Yang ZL, Yuan F, Zeng WB (2013) Systematic analyses of Ophiocordyceps lanpingensis sp. nov., a new species of Ophiocordyceps in China. Microbiol Res 168:525–532

    Article  PubMed  Google Scholar 

  • Chevallier FF (1826) Flore Générale des Environs de Paris 1. Ferra Jeune, Paris, pp1–674

  • Ciferri R (1958) Manuale di micologia medica. edn 2 . Pavia, Cortina, pp 1–178

  • Clements FE (1909) The genera of fungi, 1st edn. H.W. Wilson, Minneapolis, 114 pp

  • Cooke DEL, Drenth A, Duncan JM, Wagels G, Brasier CM (2000) A molecular phylogeny of Phytophthora and related Oomycetes. Fungal Genet Biol 30:17–32

    Article  CAS  PubMed  Google Scholar 

  • Corda ACI (1833) Die Pilze Deutschlands. In: Sturm J (ed) Deutschlands Flora in Abbildungen nach der Natur mit Beschreibungen. Sturm, Nürnberg 12:33–64

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

    Google Scholar 

  • Crous PW, Palm ME (1999) Reassessment of the anamorph genera Botryodiplodia, Dothiorella and Fusicoccum. Sydowia 51:167–175

    Google Scholar 

  • Crous PW, Verkley GJM, Christensen M, Castañeda-Ruiz RF, Groenewald JZ (2012) How important are conidial appendages? Persoonia 28:126–137

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Wingfield MJ, Schumacher RK, Summerell BA, Giraldo A, Gené J, Guarro J, Wanasinghe DN, Hyde KD, Camporesi E, Gareth Jones EB, Thambugala KM, Malysheva EF, Malysheva VF, Acharya K, Álvarez J, Alvarado P, Assefa A, Barnes CW, Bartlett JS, Blanchette RA, Burgess TI, Carlavilla JR, Coetzee MP, Damm U, Decock CA, den Breeÿen A, de Vries B, Dutta AK, Holdom DG, Rooney-Latham S, Manjón JL, Marincowitz S, Mirabolfathy M, Moreno G, Nakashima C, Papizadeh M, Shahzadeh Fazeli SA, Amoozegar MA, Romberg MK, Shivas RG, Stalpers JA, Stielow B, Stukely MJ, Swart WJ, Tan YP, van der Bank M, Wood AR, Zhang Y, Groenewald JZ (2014a) Fungal planet description sheets: 281–319. Persoonia 33:212–289

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Shivas RG, Quaedvlieg W, van der Bank M, Zhang Y, Summerell BA, Guarro J, Wingfield MJ, Wood AR, Alfenas AC, Braun U, Cano-Lira JF, García D, Marin-Felix Y, Alvarado P, Andrade JP, Armengol J, Assefa A, den Breeÿen A, Camele I, Cheewangkoon R, De Souza JT, Duong TA, Esteve-Raventós F, Fournier J, Frisullo S, García-Jiménez J, Gardiennet A, Gené J, Hernández-Restrepo M, Hirooka Y, Hospenthal DR, King A, Lechat C, Lombard L, Mang SM, Marbach PA, Marincowitz S, Marin-Felix Y, Montaño-Mata NJ, Moreno G, Perez CA, Pérez Sierra AM, Robertson JL, Roux J, Rubio E, Schumacher RK, Stchigel AM, Sutton DA, Tan YP, Thompson EH, van der Linde E, Walker AK, Walker DM, Wickes BL, Wong PT, Groenewald JZ (2014b) Fungal Planet description sheets: 214–280. Persoonia 32:184–306

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Schumacher RK, Wingfield MJ, Lombard L, Giraldo A, Christensen M, Gardiennet A, Nakashima C, Pereira OL, Smith AJ, Groenewald JZ (2015a) Fungal systematics and evolution: FUSE 1. Sydowia 67:81–118

    Google Scholar 

  • Crous PW, Müller MM, Sánchez RM, Giordano L, Bianchinotti MV, Anderson FE, Groenewald JZ (2015b) Resolving Tiarosporella spp. allied to Botryosphaeriaceae and Phacidiaceae. Phytotaxa 202:73–93

    Article  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, Gené J, Gouliamova DE, Groenewald M, Lombard L, Morozova OV, Sarkar J, Smith MT, Stchigel AM, Wiederhold NP, Alexandrova AV, Antelmi I, Armengol J, Barnes I, Cano-Lira JF, Castañeda Ruiz RF, Contu M, Courtecuisse PR, da Silveira AL, Decock CA, de Goes A, Edathodu J, Ercole E, Firmino AC, Fourie A, Fournier J, Furtado EL, Geering ADW, Gershenzon J, Giraldo A, Gramaje D, Hammerbacher A, He X-L, Haryadi D, Khemmuk W, Kovalenko AE, Krawczynski R, Laich F, Lechat C, Lopes UP, Madrid H, Malysheva EF, Marin-Felix Y, Martin MP, Mostert L, Nigro F, Pereira OL, Picillo B, Pinho DB, Popov ES, Rodas Peláez CA, Rooney-Latham S, Sandoval-Denis M, Shivas RG, Silva V, Stoilova-Disheva MM, Telleria MT, Ullah C, Unsicker SB, van der Merwe NA, Vizzini A, Wagner H-G, Wong PTW, Wood AR, Groenewald JZ (2015c) 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 B, van der Linde EJ, Vilcāne J, Voglmayr H, Wood AR (2015d) 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 

  • Crous PW, Hawksworth DL, Wingfield MJ (2015e) Identifying and naming plant-pathogenic fungi: past, present, and future. Annu Rev Phytopathol 53:247–267

    Article  CAS  PubMed  Google Scholar 

  • Cui BK, Dai YC, He SH, Zhou LW, Yuan HS (2015) A novel Phellinidium sp. causes laminated root rot on Qilian juniper (Sabina przewalskii) in Northwest China. Plant Dis 99:39–43

    Article  CAS  Google Scholar 

  • Cunningham GH (1921) The genus Cordyceps in New Zealand. Trans Proc NZ Inst 53:372–382

    Google Scholar 

  • Dai YC (2010) Hymenochaetaceae (Basidiomycota) in China. Fungal Divers 45:131–343

    Article  Google Scholar 

  • Dai YC, Cui BK, Decock C (2008) A new species of Fomitiporia (Hymenochaetaceae, Basidiomycota) from China based on morphological and molecular characters. Mycol Res 112:375–380

    Article  PubMed  Google Scholar 

  • Dai YC, Cui BK, Liu XY (2010) Bondarzewia podocarpi, a new and remarkable polypore from tropical China. Mycologia 102:881–886

    Article  PubMed  Google Scholar 

  • Dai YC, Cui BK, Yuan HS, Li BD (2007) Pathogenic wood-decaying fungi in China. Forest Pathol 37:105–120

    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 

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

    Google Scholar 

  • Das K, Chakraborty D (2014) Three interesting species of wild mushrooms from Sikkim (India). Indian J Plant Sci 3:101–108

    Google Scholar 

  • Das K, Miller SL, Sharma JR (2005) Russula in Himalaya 1: a new species of subgenus Amoenula. Mycotaxon 94:85–88

    Google Scholar 

  • Das K, Miller SL, Sharma JR (2006a) Russula in Himalaya 2: four new taxa. Mycotaxon 95:205–215

    Google Scholar 

  • Das K, Sharma JR, Atri NS (2006b) Russula in Himalaya 3: a new species of subgenus Ingratula. Mycotaxon 95:271–275

    Google Scholar 

  • Das K, Putte VDP, Buyck B (2010) New or interesting Russula from Sikkim Himalaya (India). Cryptog Mycol 31:373–387

    Google Scholar 

  • Das K, Atri NS, Buyck B (2013) Three new Russula (Russulales) from India. Mycosphere 4:722–732

    Article  Google Scholar 

  • Das K, Dowie NJ, Li GJ, Miller SL (2014) Two new species of Russula (Russulales) from India. Mycosphere 5:612–622

    Google Scholar 

  • de Almeida DAC, Gusmão LFP, Miller AN (2014) A new genus and three new species of hysteriaceous ascomycetes from the semiarid region of Brazil. Phytotaxa 176:298–308

    Article  Google Scholar 

  • De Bertoldi M, Lepidi AA, Nuti MP (1972) Classification of the genus Humicola Traaen I. preliminary reports and investigations. Mycopathologia 46:289–304

    Google Scholar 

  • De Crop E, Nuytinck J, Van de Putte K, Lecomte M, Eberhardt U, Verbeken A (2014) Lactifluus piperatus (Russulales, Basidiomycota) and allied species in Western Europe and a preliminary overview of the group worldwide. Mycol Prog 13:493–511

    Article  Google Scholar 

  • De Crop E, Nuytinck J, Van de Putte K et al (subm.) A multi-gene phylogeny of Lactifluus (Basidiomycota, Russulales) translated into a new infrageneric classification of the genus. Mycol Prog (In press)

  • De Gruyter JD, Woudenberg JHC, Aveskamp AA, Verkley GJM, Groenewald JZ, Crous PW (2012) Redisposition ofPhoma-like anamorphs in Pleosporales. Stud Mycol 75:1–36

    Article  PubMed Central  Google Scholar 

  • Decock C, Figueroa SH, Robledo G, Castillo G (2007) Fomitiporia punctata (Basidiomycota, Hymenochaetales) and its presumed taxonomic synonyms in America: taxonomy and phylogeny of some species from tropical/subtropical areas. Mycologia 99:733–752

    Article  CAS  PubMed  Google Scholar 

  • Dexter Y, Cooke RC (1984) Fatty acids, sterols and catotenoids of the psychrophile Mucor strictus and some mesophilic Mucor species. Trans Brit Mycol Soc 83:455–461

    Article  CAS  Google Scholar 

  • Doweld AB (2012) (2068–2070) Proposals to conserve Pertusariaceae against Variolariaceae, Chrysothrichaceae against Pulverariaceae and Dothioraceae against Saccotheciaceae (Fungi) with revision of dates of publication given in Taxonomic Literature II. Taxon 61:681–682

    Google Scholar 

  • Du Y, Shi P, Huang H, Zhang X, Luo H, Wang Y, Yao B (2013) Characterization of three novel thermophilic xylanase from Humicola insolens Y1 with application potentials in the brewing industry. Bioresou Tech 130:161–167

    Article  CAS  Google Scholar 

  • Duhem B, Michel H (2009) Une espèce nouvelle de Corticium s.st. Études dans les genres Dendrocorticium et Dentocorticium (Basidiomycotina). Cryptogam Mycol 30:161–179

    Google Scholar 

  • Eberhardt U (2002) Molecular kinship analyses of the agaricoid Russulaceae: correspondence with mycorrhizal anatomy and sporocarp features in the genus Russula. Mycol Prog 1:201–223

    Article  Google Scholar 

  • Ellis MB (1971) Dematiaceous hyphomycetes. Commonwealth Mycological Institute, Kew

    Google Scholar 

  • Ertz D, Diederich P, Lawrev JD, Berger F, Freebury CE, Coppins B, Gardiennet A, Hafellner J (2015) Phylogenetic insights resolve Dacampiaceae (Pleosporales) as polyphyletic: Didymocyrtis (Pleosporales, Phaeosphaeriaceae) with Phoma-like anamorphs resurrected and segregated from Polycoccum (Trypetheliales, Polycoccaceae fam. nov.). Fungal Divers 74:53–89

    Article  Google Scholar 

  • Fan XL, Liang YM, Ma R, Tian CM (2014a) Morphological and phylogenetic studies of Cytospora (Valsaceae, Diaporthales) isolates from Chinese scholar tree, with description of a new species. Mycoscience 55:252–259

    Article  Google Scholar 

  • Fan XL, Tian CM, Yang Q, Liang YM, You CJ, Zhang YB (2014b) Cytospora from Salix in northern China. Mycotaxon 129:303–315

    Article  Google Scholar 

  • Fan XL, Hyde KD, Liu M et al. (2015a) Cytospora species associated with walnut canker disease in China, with description of a new species C. gigalocus. Fungal Biol 119:310–319

  • Fan XL, Hyde KD, Yang Q, Liang YM, Ma R, Tian CM (2015b) Cytospora species associated with canker disease of three antidesertification plants in northwestern China. Phytotaxa 197:227–244

    Article  Google Scholar 

  • Farr DF, Rossman AY (2015) Fungal databases, systematic mycology and microbiology laboratory, ARS, USDA. Retrieved January 11, 2015, from http://nt.ars-grin.gov/fungaldatabases/

  • Fell JW, Master IM (1975) Phycomycetes (Phytophthora spp. nov. and Pythium sp. nov.) associated with degrading mangrove (Rhizophora mangle) leaves. Can J Bot 53:2908–2922

    Article  Google Scholar 

  • Fernández FA, Huhndorf SM (2005) New species of Chaetosphaeria, Melanopsammella and Tainosphaeria gen. nov. from the Americas. Fungal Divers 18:15–57

    Google Scholar 

  • Fernández FA, Miller AN, Huhndorf SM, Lutzoni FM, Zoller S (2006) Systematics of the genus Chaetosphaeria and its allied genera: morphological and phylogenetic diversity in north temperate and neotropical taxa. Mycologia 98:121–130

    Article  PubMed  Google Scholar 

  • Ferreira JHS (1987) Dieback of grapevines in South Africa. PhD Thesis, University of the Western Cape, South Africa

  • Fidalgo O (1968) Phellinus pachyphloeus and its allies. Mem NY Bot Gard 17:109–147

    Google Scholar 

  • Fliegerová K, Hodrová B, Voigt K (2004) Classical and molecular approaches as a powerful tool for the characterization of rumen polycentric fungi. Folia Microbiol (Praha) 49:157–164

    Article  Google Scholar 

  • Fliegerová K, Mrázek J, Hoffmann K, Zábranská J, Voigt K (2010) Diversity of anaerobic fungi within cow manure determined by ITS1 analysis. Folia Microbiol (Praha) 55:319–325

    Article  CAS  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 

  • Fries EM (1823) Systema mycologicum vol 2. Greifswald, Germany. (in Latin)

  • Fries GE (1874) Hymenomycetes. Eur. Ed. Berling, Uppsala

  • Frye CB, Reinhardt DJ (1993) Characterization of groups of the Zygomycete genus Rhizopus. Mycopathologia 124:139–147

    Article  Google Scholar 

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

    Google Scholar 

  • Fujimura R, Nishimura A, Ohshima S, Sato Y, Nishizawa T, Oshima K, Hattori M, Narisawa K, Ohta H (2014) Draft genome sequence of the betaproteobacterialendosymbiont associated with the fungus Mortierella elongata FMR23-6. Genome Announce 2:e01272–14

    Article  Google Scholar 

  • Fungal Names (2016) http://124.16.146.175:8080/checklist/checklist.html. Accessed on Mar 2016

  • Gaillard-Martinie B, Breton A, Dusser M, Julliand V (1995) Piromyces citronii sp. nov., a strictly anaerobic fungus from the equine caecum: a morphological, metabolic, and ultrastructural study. FEMS Microbiol Lett 130:321–326

    Article  CAS  Google Scholar 

  • Gams W (1976) Some new or noteworthy species of Mortierella. Persoonia 9:111–140

    Google Scholar 

  • Gams W (1977) A key to the species of Mortierella. Persoonia 9:381–391

    Google Scholar 

  • Garnica S, Weiss M, Walther G, Oberwinkler F (2007) Reconstructing the evolution of agarics from nuclear gene sequences and basidiospore ultrastructure. Mycol Res 111:1019–1029

    Article  CAS  PubMed  Google Scholar 

  • Garnica S, Spahn P, Oertel B, Ammirati J, Oberwinkler F (2011) Tracking the evolutionary history of Cortinarius species in section Calochroi, with transoceanic disjunct distributions. BMC Evol Biol 11:213–231

    Article  PubMed  PubMed Central  Google Scholar 

  • Gelardi M, Vizzini A, Ercole E, Voyron S, Sun JZ, Liu XZ (2013) Boletus sinopulverulentus, a new species from Shaanxi Province (central China) and notes on Boletus and Xerocomus. Sydowia 65:45–57

    Google Scholar 

  • Ghobad-Nejhad M, Nilsson RH, Hallenberg N (2010) Phylogeny and taxonomy of the genus Vuilleminia (Basidiomycota) based on molecular and morphological evidence, with new insights into Corticiales. Taxon 59:1519–1534

    Google Scholar 

  • Gold JJ, Heath IB, Bauchop T (1988) Ultrastructural description of a new chytrid genus of caecum anaerobe, Caecomyces equi gen. nov., sp. nov., assigned to the Neocallimasticaceae. Biosystems 21:403–415

    Article  CAS  PubMed  Google Scholar 

  • Gorjón SP, Saitta A (2014) Leptocorticium gloeocystidiatum sp. nov. (Corticiales, Basidiomycota), a new corticioid fungus from Sicily, Italy. Mycosphere 5:406–409

    Article  Google Scholar 

  • Grove WB (1937) British stem-and leaf-fungi (Coelomycetes). Vol. II. Cambridge at the University Press, Cambridge

  • Gruninger RJ, Puniya AK, Callaghan TM, Edwards JE, Youssef N, Dagar SS, Fliegerova K, Griffith GW, Forster R, Tsang A, McAllister T, Elshahed MS (2014) Anaerobic Fungi (Phylum Neocallimastigomycota): advances in understanding of their taxonomy, life cycle, ecology, role, and biotechnological potential. FEMS Microbiol Ecol 90:1–17

    Article  CAS  PubMed  Google Scholar 

  • Guindon S, Gascuel O (2003) A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol 52:679–704

    Article  Google Scholar 

  • Guindon S, Dufayard JF, Lefort V, Anisimova M, Hordijk W, Gascuel O (2010) New algorithms and methods to estimate maximum likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol 59:307–321

    Article  CAS  PubMed  Google Scholar 

  • Gvritishvili MN (1982) The fungal genus Cytospora in the USSR. Izdatelstve Sabchota Sakarstvelo, Tbilisi

    Google Scholar 

  • Hall T (2004) BioEdit. Ibis Therapeutics, Carlsbad, CA, 92008, USA. http://www.mbio.ncsu.edu/BioEdit/bioedit.html. 18 Mar 2005

  • Hallenberg N (1980) New taxa of Corticiaceae from N. Iran (Basidiomycetes). Mycotaxon 11:447–475

    Google Scholar 

  • Hallenberg N (2012) Leptocorticium tenellum (Agaricomycetes) found in Chile. Kurtziana 37:109–112

    Google Scholar 

  • Hansen EM, Reeser PW, Sutton W (2012) Phytophthora borealis and Phytophthora riparia, new species in Phytophthora ITS Clade 6. Mycologia 104:1133–1142

    Article  PubMed  Google Scholar 

  • Hao YJ, Qin J, Yang ZL (2014) Cibaomyces, a new genus of Physalacriaceae from East Asia. Phytotaxa 162:198–210

    Article  Google Scholar 

  • Hardham AR (2009) The asexual life cycle. In: Lamour K, Kamoun S (eds) Oomycete genetics and genomics: diversity, interactions, and research tools. Wiley, Hoboken, pp 93–119

    Chapter  Google Scholar 

  • Harrower E, Ammirati JF, Cappuccino AA, Ceska O, Kranabetter JM, Kroeger P, Lim S, Taylor T, Berbee ML (2011) Cortinarius species diversity in British Columbia and molecular phylogenetic comparison with European specimen sequences. Botany 89:799–810

    Article  Google Scholar 

  • Hashimoto A, Sato G, Matsuda T, Hirayama K, Hatakeyama S, Harada Y, Shirouzu T, Tanaka K (2015a) Molecular taxonomy of Dinemasporium and its allied genera. Mycoscience 56:86–101

    Article  Google Scholar 

  • Hashimoto A, Sato G, Matsuda T, Matsumura M, Hatakeyama S, Harada Y, Tanaka K (2015b) Taxonomic revision of Pseudolachnea and Pseudolachnella and establishment of Neopseudolachnella and Pseudodinemasporium gen. nov. Mycologia 107:383–408

    Article  PubMed  Google Scholar 

  • Hawksworth DL (1982) A new species of Caryospora from Eugenia in East Africa. Trans Br Mycol Soc 79:69–74

    Article  Google Scholar 

  • Hawksworth DL, Eriksson O (1988) (895) – (906) Proposal to conserve 11 family names in the Ascomycotina (Fungi). Taxon 37:190–193

    Article  Google Scholar 

  • He MQ, Zhao RL (2015) A new species of Agaricus section Minores from China. Mycology 6:182–186

    Article  Google Scholar 

  • Heath IB, Bauchop T, Skipp RA (1983) Assignment of the rumen anaerobe Neocallimastix frontalis to the Spizellomycetales (Chytridiomycetes) on the basis of its polyflagellate zoospore ultrastructure. Can J Bot 61:295–307

    Article  Google Scholar 

  • Heinemann P (1978) Essai d’une clé de détermination des genres Agaricus et Micropsalliota. Sydowia 30:6–37

    Google Scholar 

  • Hermet A, Méheust D, Monunier J, Barbier G, Jany JL (2012) Molecular systematics in the genus Mucor with special regards to species encountered in cheese. Fungal Biol 116:692–705

    Article  PubMed  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 

  • Hibbett DS, Binder M, Bischoff JF, Blackwell M, Cannon PF, Eriksson OE, Huhndorf S, James T, Kirk PM, Lucking R, Thorsten Lumbsch H, Lutzoni F, Matheny PB, McLaughlin DJ, Powell MJ, Redhead S, Schoch CL, Spatafora JW, Stalpers JA, Vilgalys R, Aime MC, Aptroot A, Bauer R, Begerow D, Benny GL, Castlebury LA, Crous PW, Day Y-C, Gams W, Geiser DM, Griffith GW, Gueidan C, Hawksworth DL, Hestmark G, Hosaka K, Humber RA, Hyde KD, Ironside IE, Koljalg U, Kurtzman CP, Larsson K-H, Lichtwardt R, Longcore J, Miądlikowska J, Miller A, Moncalvo J-M, Mozley-Standtridge S, Oberwinkler F, Parmasto E, Reeb W, Rogers J-D, Roux C, Ryvarden L, Sampaio JP, Schussler A, Sugiyama J, Thorn RG, Tibell L, Untereiner WA, Walker C, Wang Z, Weir A, Weiss M, White MM, Winka K, Yao Y-J, Zhang N (2007) A higher- level phylogenetic classification of the Fungi. Mycol Res 111:509–547

    Article  PubMed  Google Scholar 

  • Hino I, Katumoto K (1958) On Chaetopatella, a new genus of the Excipulaceae. J Jpn Bot 33:233–239

    Google Scholar 

  • Hirayama K, Tanaka K, Raja HA, Miller AN, Shearer CA (2010) A molecular phylogenetic assessment of Massarina ingoldianasensu lato. Mycologia 102:729–746

    Article  CAS  PubMed  Google Scholar 

  • Ho HM, Chen ZC (1990) Morphological study of Gongronella butleri (Mucorales) from Taiwan. Taiwania 35:259–263

    Google Scholar 

  • Ho HM, Chuang SC, Chen SJ (2004) Notes on Zygomycetes of Taiwan (IV): three Absidia species (Mucoraceae). Fung Sci 19:125–131

    Google Scholar 

  • Ho YW, Barr DJS, Abdullah N, Jalaluldin S, Kudo H (1993a) A new species of Piromyces from the rumen of deer in Malaysia. Mycotaxon 47:285–293

    Google Scholar 

  • Ho YW, Barr DJS, Abdullah N, Jalaluldin S, Kudo H (1993b) Piromyces spiralis, a new species of anaerobic fungus from the rumen of goat. Mycotaxon 48:59–68

    Google Scholar 

  • Hodhod MS, Abdel-Wahab MA, Bahkali AH, Hyde KD (2012) Amergraphium solium sp. nov. from Yanbu mangroves in the Kingdom of Saudi Arabia. Cryptogam Mycol 33:285–294

    Article  Google Scholar 

  • Hoffmann K, Voigt K (2009) Absidia parricida plays a dominant role in biotrophic fusion parasitism among mucoralean fungi (Zygomycetes): Lentamyces, a new genus for A. parricida and A. zychae. Plant Biol 4:537–554

    Article  CAS  Google Scholar 

  • Hoffmann K, Discher S, Voigt K (2007) Revision of the genus Absidia (Mucorales, Zygomycetes) based on physiological, phylogenetic, and morphological characters; thermotolerant Absidia spp. form a coherent group, Mycocladiaceae fam. nov. Mycol Res 111:1169–1183

    Article  CAS  PubMed  Google Scholar 

  • Hoffmann K, Voigt K, Kirk P (2011) Mortierellomycotina subphyl. nov., based on multi-gene genealogies. Mycotaxon 115:353–363

    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 

  • Hofstetter V, Clémençon H, Vilgalys R, Moncalvo J-M (2002) Phylogenetic analyses of the Lyophylleae (Agaricales, Basidiomycota) based on nuclear and mitochondrial rDNA sequences. Mycol Res 106:104–1059

    Article  CAS  Google Scholar 

  • von Höhnel F (1918) Mycologische Fragmente, 272. Über die Hysteriaceen. Ann Mycol 16:145–154

    Google Scholar 

  • Höhnel F (1919) Fünfte vorläufige Mitteilung mykologische Ergebnisse (Nr. 300–500). Berichte der Deutschen Botanischen Gesellschaft 37:153–161

    Google Scholar 

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

    Article  Google Scholar 

  • Holm L, Holm K (1988) Studies in the Lophiostomataceae with emphasis on the Swedish species. Symb Bot Upsal 28:1–50

    Google Scholar 

  • Hong CX, Gallegly ME, Richardson PA, Kong P, Moorman GW, Lea-Cox JD, Ross DS (2010) Phytophthora hydropathica, a new pathogen identified from irrigation water, Rhododendron catawbiense and Kalmia latifolia. Plant Pathol 59:913–921

    Article  CAS  Google Scholar 

  • Hong CX, Richardson PA, Hao W, Ghimire SR, Kong P, Moorman GW, Lea-Cox JD, Ross DS (2012) Phytophthora aquimorbida sp. nov. and Phytophthora taxon ‘aquatilis’ recovered from irrigation reservoirs and a stream in Virginia, USA. Mycologia 104:1097–1108

    Article  PubMed  Google Scholar 

  • Hongo T (1982) The Amanitas of Japan. Acta Phytotaxon Geobot 33:116–126

    Google Scholar 

  • Hosen MI, Ge ZW (2011) Clarkeinda trachodes (Agaricales, Basidiomycetes), first record from Bangladesh. Mycotaxon 118:331–336

    Article  Google Scholar 

  • Hongsanan S, Tian Q, Peršoh D, Zeng XY, Hyde KD, Chomnunti P, Boonmee S, Bahkali AH, Wen TC (2015) Meliolales. Fungal Divers 74:91–141

    Article  Google Scholar 

  • Hsieh HM, Ju YM, Rogers JD (2005) Molecular phylogeny of Hypoxylon and closely related genera. Mycologia 97:844–865

    Article  CAS  PubMed  Google Scholar 

  • Hundorf SM, Miller AN, Fernández FA (2004) Molecular systematics of the Coronophorales and new species of Bertia, Lasiobertia and Nitschkia. Mycol Res 108:1384–1398

    Article  CAS  Google Scholar 

  • Hyde KD (1990) A new marine ascomycete from Brunei. Aniptodera longispora sp. nov. from intertidal mangrove wood. Bot Mar 33:335–338

    Article  Google Scholar 

  • Hyde KD (2002) Aniptodera triseptata sp. nov. (Halosphaeriales) from submerged wood in freshwater. Cryptogam Mycol 23:5–7

    Google Scholar 

  • Hyde KD, Ho WH, Tsui CKM (1999) The genera Aniptodera, Halosarpheia, Nais and Phaeonectriella from freshwater habitats. Mycoscience 40:165–183

    Article  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

    Article  Google Scholar 

  • 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, Abd-Elsalam K, Cai L (2010) Morphology: still essential in a molecular world. Mycotaxon 114:439–451

    Article  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 Y-X, Lucking R, Monkai 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, Aguirre-Hudson B, Alias SA, Aptroot A, Bahkali AH, Bezerra JL, Bhat DJ, Camporesi E, Chukeatirote E, Gueidan C, Hawksworth DL, Hirayama K, De Hoog S, Kang JC, 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, Zhang 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 

  • Index Fungorum (2016) http://www.indexfungorum.org/Names/Names.asp. Accessed on Mar 2016

  • Jacobs K, Botha A (2008) Mucor renisporus sp. nov., a new coprophilous species from Southern Africa. Fungal Divers 29:27–35

    Google Scholar 

  • Jaklitsch W, Baral HO, Lücking R, Lumbsch HT (2016) Engler’s syllabus of plant families. In: Frey W (ed) Part 1/2: Ascomycota, 13th edn. Borntraeger, Stuttgart

    Google Scholar 

  • Jami F, Slippers B, Wingfield MJ, Gryzenhout M (2012) Five new species of the Botryosphaeriaceae from Acacia karroo in South Africa. Cryptogam Mycol 33:245–266

    Article  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 

  • Jeewon R, Yeung SYQ, Hyde KD (2009) A novel phylogenetic group within Thozetella (Chaetosphaeriaceae): a new taxon based on morphology and DNA sequence analyses. Can J Microbiol 55:680–687

    CAS  PubMed  Google Scholar 

  • Jones EBG (1995) Ultrastructure and taxonomy of the aquatic ascomycetous order Halosphaeriales. Can J Bot 73(Suppl 1):S790–S801

    Article  Google Scholar 

  • Jones EBG, Sakayaroj J, Suetrong S, Somrithipol S, Pang KL (2009) Classification of marine Ascomycota, anamorphic taxa and Basidiomycota. Fungal Divers 35:1–203

    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 

  • Ju YM, Rogers JD (1996) A revision of the genus Hypoxylon. Mycologia Memoir no. 20. APS Press, St. Paul, 365

  • Ju YM, Hsieh HM, Ho MC, Szu DH, Fang MJ (2007) Theissenia rogersii sp. nov. and phylogenetic position of Theissenia. Mycologia 66:612–621

    Article  Google Scholar 

  • Judelson HS (2009) Sexual reproduction in Oomycetes: biology, diversity, and contributions to fitness. In: Lamour K, Kamoun S (eds) Oomycete genetics and genomics: diversity, interactions, and research tools. Wiley, Hoboken, pp 121–138

    Chapter  Google Scholar 

  • Kamoun S (2003) Molecular genetics of pathogenic oomycetes. Eukaryot Cell 2:191–199

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Karadžić D (2003) Tiarosporella species: distribution and significance. Glasnik Sumarskog Fakulteta 87:9–23

    Article  Google Scholar 

  • Karsten PA (1881) Enumeralio boletinearum et polypore arum fennicarum, systemate novo dispositarum. Rev Mycol 3:16–19

    Google Scholar 

  • Karunarathna SC, Yang ZL, Zhao R, 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 

  • Kepler RM, Sung GH, Harada Y, Tanaka K, Tanaka E, Hosoya T, Bischoff JF, Spatafora JW (2012) Host jumping onto close relatives and across Kingdoms by Tyrannicordyceps (Clavicipitaceae) gen. nov. and Ustilaginoidea (Clavicipitaceae). Am J Bot 99:552–561

    Article  CAS  PubMed  Google Scholar 

  • Kepler RM, Humber RA, Bischoff JF, Rehner SA (2014) Clarification of generic and species boundaries for Metarhizium and related fungi through multi-gene phylogenetics. Mycologia 106:811–29

    Article  PubMed  Google Scholar 

  • Kirisits T (2007) Die Petrakia-Blattbräune des Bergahorns. Forstschutz Aktuell (Wien) 40:28–31

    Google Scholar 

  • Knapp DG, Kovács GM, Zajta E, Groenewald JZ, Crous PW (2015) Dark septate endophytic pleosporalean genera from semiarid areas. Persoonia 35:87–100

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kobayashi Y (1979) The genus Cordyceps and its allies from Taiwan (Formosa). Bull Nat Sci Mus Ser B (Tokyo) 7:113–122

    Google Scholar 

  • Kraichak E, Divakar PK, Crespo A, Leavitt SD, Nelsen MP, Lücking R, Lumbsch HT (2015) A tale of two hyper-diversities: diversification dynamics of the two largest families of lichenized fungi. Sci Rep 5:10028

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kränzlin F (2005) Fungi of Switzerland, 6, Russulaceae: Lactarius, Russula. Verlag Mykologia, Luzern

    Google Scholar 

  • Kroon LPNM, Bakker FT, Van den Bosch GBM, Bonants PJM, Flier WG (2004) Phylogenetic analysis of Phytophthora species based on mitochondrial and nuclear DNA sequences. Fungal Genet Biol 41:766–782

    Article  CAS  PubMed  Google Scholar 

  • Kroon LPNM, Brouwer H, de Cock AWAM, Govers F (2012) The genus Phytophthora anno 2012. Phytopathology 102:348–364

    Article  PubMed  Google Scholar 

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

    Google Scholar 

  • Kirk PM, Stalpers JA, Braun E, Crous PW, Hansen K (2013) A without-prejudice list of generic names of fungi for protection under the International Code of Nomenclature for algae, fungi, and plants. IMA Fungus 4:381–443

    Article  PubMed  PubMed Central  Google Scholar 

  • Ko WH, Yang CH, Lin MJ, Chen CY, Tsou YJ (2011) Humicola phialophoroides sp. nov. from soil with potential for biological control of plant disease. Bot Stud 52:197–202

    Google Scholar 

  • Kohlmeyer J, Kohlmeyer E (1979) Marine mycology. the higher fungi. Academic Press, New York

    Google Scholar 

  • Kohlmeyer J, Volkman-Kohlmeyer B (1987) Marine fungi of Aldabra, the Galapago, and other tropical islands. Can J Bot 65:571–582

    Article  Google Scholar 

  • Kornerup A, Wanscher JH (1978) Methuen handbook of colour, 3rd edn. Methuen, London

    Google Scholar 

  • Kornerup A, Wanscher JH (1981) Taschenlexikon der Farben, 3rd edn. Muster-Schmidt Verlag, Göttingen

    Google Scholar 

  • Kuhnert E, Fournier J, Peršoh D, Luangsa-ard JJD, Stadler M (2014) New Hypoxylon species from Martinique and new evidence on the molecular phylogeny of Hypoxylon based on ITS rDNA and β-tubulin data. Fungal Divers 64:81–203

    Article  Google Scholar 

  • Kuhnert E, Surup F, Sir EB, Lambert C, Hyde KD, Hladki AI, Romero AI, Stadler M (2016) Lenormandins A – G, new azaphilones from Hypoxylon lenormandii and Hypoxylon jaklitschii sp. nov., recognised by chemotaxonomic data. Fungal Divers 71:165–184

    Article  Google Scholar 

  • Kundsen H, Borgen T (1982) Russlaceae in Greenland. In: Artic and Alpine Mycology 216–236

  • Kuntze O (1891) Revisio generum plantarum (in Latin) 2. A. Felix, Leipzig, 848 pp

    Google Scholar 

  • Kwasna H, Ward E, Bateman GL (2006) Phylogenetic relationships among Zygomycetes from soil based on ITS1/2 rDNA sequences. Mycol Res 110:501–510

    Article  CAS  PubMed  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 KH (2007) Re-thinking the classification of corticioid fungi. Mycol Res 111:1040–1063

    Article  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 

  • Læssøe T, Spooner BM (1994) Rosellinia & Astrocystis (Xylariaceae): new species and generic concepts. Kew Bull 49:1–70

    Article  Google Scholar 

  • Læssøe T, Srikitikulchai P, Luangsa-ard JJ, Stadler M (2013) Theissenia reconsidered, including molecular phylogeny of the type species T. pyrenocrata and a new genus Durotheca (Xylariaceae, Ascomycota). IMA Fungus 4:57–69

    Article  PubMed  PubMed Central  Google Scholar 

  • Le HT, Verbeken A, Nuytinck J, Lumyong S, Desjardin DE (2007) Lactarius in Northern Thailand: 3. Lactarius subgenus Lactoriopsis. Mycotaxon 102:281–291

    Google Scholar 

  • Lebel T, Tonkin JE (2007) Australasian species of Macowanites are sequestrate species of Russula. Aust Syst Bot 20:355–381

    Article  Google Scholar 

  • Lebel T (2013) Two new species of sequestrate Agaricus (section Minores) from Australia. Mycol Prog 12:699–707

    Article  Google Scholar 

  • Lechat C (2010) Ochronectria courtecuissei sp. nov. Bull Soc Mycol Fr 126:97–101

    Google Scholar 

  • Leelavathy KM, Zachariah S, Sankaran KV (1981) Clarkeinda rhacodes a new record from India. Mycologia 73:204–207

    Article  Google Scholar 

  • Li GJ (2014) Taxonomy of Russula from China. Ph.D. dissertation. Institute of Microbiology, Chinese Academy of Sciences & University of Chinese Academy of Sciences (In Chinese)

  • Li GJ, Wen HA (2009) Research of prospects on taxonomy of the Russula in China. Mycosystema 28:303–309 (In Chinese)

    CAS  Google Scholar 

  • Li GJ, Li SF, Wen HA (2011a) Russula zhejiangensis sp. nov. from East China. Cryptogam Mycol 32:127–133

    Article  CAS  Google Scholar 

  • Li GJ, Li SF, Liu XZ, Wen HA (2012) Russula jilinensis sp. nov. (Russulaceae) from northeast China. Mycotaxon 120:49–58

    Article  Google Scholar 

  • Li GJ, Zhao Q, Zhao D, Yue SF, Li SF, Wen HA, Liu XZ (2013a) Russula atroaeruginea and R. sichuanensis spp. nov. from southwest China. Mycotaxon 124:137–188

    Google Scholar 

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

    Article  Google Scholar 

  • Li GJ, Zhao D, Li SF, Wen HA (2015a) Russula chiui and R. pseudopectinatoides, two new species from southwestern China supported by morphological and molecular evidence. Mycol Prog 14:33

    Article  Google Scholar 

  • Li GJ, Li SF, Zhao D, Wen HA (2015b) Recent research progress of Russula (Russulales, Agaricomycetes): a review. Mycosystema 34:821–848 (In Chinese)

  • Li J, Heath IB, Bauchop T (1990) Piromyces mae and Piromyces dumbonica, two new species of uniflagellate anaerobic chytridiomycete fungi from the hindgut of the horse and elephant. Can J Bot 68:1021–1033

    Article  Google Scholar 

  • Li J, Zhang J, Chen H, Chen X, Lan J (2013c) Complete Mitochondrial Genome of the Medicinal Mushroom Ganoderma lucidum. PLoS ONE 8:72038

    Article  CAS  Google Scholar 

  • Li WJ, Liu JK, Bhat DJ, Camporesi E, Xu J, Hyde KD (2014a) Introducing the novel species, Dothiorella symphoricarposicola, from snowberry in Italy. Cryptogam Mycol 35:257–270

    Article  Google Scholar 

  • Li WJ, Bhat DJ, Camporesi E, Tian Q, Wijayawardene NN, Dai DQ, Phookamsak R, Chomnunti P, Bahkali AH, Hyde KD (2015c) New asexual morph taxa in Phaeosphaeriaceae. Mycosphere 6:681–708

    Google Scholar 

  • Li YC, Yang ZL, Tolgor B (2009) Phylogenetic and biogeographic relationships of Chroogomphus species as inferred from molecular and morphological data. Fungal Divers 38:85–104

    Google Scholar 

  • Li YC, Feng B, Yang ZL (2011b) Zangia, a new genus of Boletaceae supported by molecular and morphological evidence. Fungal Divers 49:125–143

    Article  Google Scholar 

  • Li YC, Ortiz-Santana B, Zeng NK, Feng B, Yang ZL (2014b) Molecular phylogeny and taxonomy of the genus Veloporphyrellus. Mycologia 106:291–306

    Article  PubMed  Google Scholar 

  • Li YK, Zhang X, Yuan Y, Cao Z, Liang JF (2015d) Morphological and molecular evidence for a new species of Russula (Russulaceae) from southern China. Phytotaxa 202:94–102

    Article  Google Scholar 

  • Liang ZQ (2007) Cordyceps. Flora Fungorum Sinicorum, vol 32. Science Press, Beijing, pp 1–190

    Google Scholar 

  • Liebetanz E (1910) Die parasitischen Protozoen des Wiederkäuermagens. Arch Für Protistenkd 19:19–80

    Google Scholar 

  • Liew ECY, Aptroot A, Hyde KD (2002) An evaluation of the monophyly of Massarina based on ribosomal DNA sequences. Mycologia 94:803–813

    Article  CAS  PubMed  Google Scholar 

  • Liimatainen K (2015) Nomenclatural novelties, Cortinarius. Index Fungorum no. 241

  • Linaldeddu BT, Deidda A, Scanu B, Franceschini A, Serra S, Berraf-Tebbal A, Zouaoui Boutiti M, Jamâa MLB, Phillips AJL (2015) Diversity of Botryosphaeriaceae species associated with grapevine and other woody hosts in Italy, Algeria and Tunisia, with descriptions of Lasiodiplodia exigua and Lasiodiplodia mediterranea sp. nov. Fungal Divers 71:201–204

    Article  Google Scholar 

  • Lindau G (1897) Pyrenomycetineae, Laboulbeniineae. In Engler A, Prantl K (eds) Die Natürlichen Pflanzenfamilien. Teil. 1 1 (1):321–505. Leipzig; Verlag von Wilhelm Engelmann

  • Liu JK, Phookamsak R, Doilom M, Wikee S, Li YM, Ariyawansha H, Boonmee S, Chomnunti P, Dai DQ, Bhat JD, Romero AI, Zhuang WY, Monkai J, Jones EBG, Chukeatirote E, KoKo TW, Zhao YC, Wang Y, Hyde KD (2012) Towards a natural classification of Botryosphaeriales. Fungal Divers 57:149–210

    Article  Google Scholar 

  • Liu JK, Hyde KD, Jones EBG, Ariyawansa HA, Bhat JD, 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, D’souza MJ, Fan XL, Goonasekara ID, Hirayama K, Hongsanan S, Jayasiri SC, Jayawardena RS, Karunarathana SC, Li WJ, Mapook A, Norphanphoun C, Pang KL, Perera RH, Peršoh D, Pinruan U, Senanayake IC, Somrithipol S, Suetrong S, Tanaka K, Thambugala KM, Tian Q, Tibpromma S, Udayanga D, Wuayawardene NN, Wanasinghe D, 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 XL, Liu XX, Liu ZY, Matsumura M, Mortimer PE, Rambold G, Randrianjohany E, Sato G, Sriindrasutdhi V, Tian CM, Verbeken A, Von Brackel W, Wang Y, Wen TC, Xu JC, Yan JY, Zhao RL, Camporesi E (2015) Fungal diversity notes 1–110: Taxonomic and phylogenetic contributions to fungal species. Fungal Divers 72:1–197

    Article  CAS  Google Scholar 

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

    Google Scholar 

  • Lodge DJ, Padamsee M, Matheny PB, Aime MC, Cantrell SA, Boertmann D, Kovalenko A, Vizzini A, Dentinger BTM, Kirk PM, Ainsworth AM, Moncalvo J-M, Vilgalys R, Larsson E, Lücking R, Griffith GW, Smith ME, Norvell LL, Desjardin DE, Redhead SA, Ovrebo CL, Lickey EB, Ercole E, Hughes KW, Courtecuisse R, Young A, Binder M, Minnis AM, Lindner DL, Ortiz-Santana B, Haight J, Læssøe T, Baroni TJ, Geml J, Hattori T (2014) Molecular phylogeny, morphology, pigment chemistry and ecology in Hygrophoraceae (Agaricales). Fungal Divers 64:1–99

    Article  Google Scholar 

  • Luangsa-ard JJ, Tasanathai K, Mongkolsamrit S, Hywel-Jones NL (2007) Atlas of invertebrate-pathogenic fungi of Thailand, vol 1. BIOTEC, National Science and Tecnology Development Agency, Thailand

    Google Scholar 

  • Lücking R (2014) A key to species of the Ocellularia papillata, perforata and terebrata morphodemes (Ascomycota: Graphidaceae). Glalia 6:1–35

    Google Scholar 

  • Lücking R (2015) Thelotremoid Graphidaceae from the NYBG herbarium: new species, range extensions, and a forgotten lichen. Opusc Philolich 14:1–57

    Google Scholar 

  • Lücking R, Pérez-Ortega S (2015) Four new species of Ocellularia (lichenized Ascomycota: Graphidaceae) from Cuba, with a revised taxonomy of the O. bahiana complex and a key to thelotremoid taxa with small, brown, (sub-) muriform ascospores. Lichenologist 47:305–322

    Article  Google Scholar 

  • Lücking R, Johnston MK, Aptroot A, Kraichak E, Lendemer JC, Boonpragob K, Cáceres MES, Ertz D, Ferraro LI, Jia ZF, Kalb K, Mangold A, Manoch L, Mercado-Díaz JA, Moncada B, Mongkolsuk P, Papong K, Parnmen S, Peláez R, Poengsoengnoen V, Rivas Plata E, Saipunkaew W, Sipman HJM, Suttjaritturakan J, Van den Broeck D, von Konrat M, Weerakoon G, Lumbsch HT (2014) One hundred and sventy five new species of Graphidaceae: closing the gap or a drop in the bucket? Phytotaxa 189:7–38

    Article  Google Scholar 

  • Lumbsch HT, Huhndorf SM (2010) Outline of Ascomycota – 2009. Fieldiana Life Earth Sci 1:1–60

    Article  Google Scholar 

  • Luque J, Sierra D, Torres E, Garcia F (2006) Cryptovalsa ampelina on grapevines in N.E. Spain: identification and pathogenicity. Phytopathol Mediterr 45:S101–S109

    Google Scholar 

  • Maerz A, Paul MR (1950) A dictionary of color. McGraw-Hill book Company, USA

    Google Scholar 

  • Madden AA, Stchigel AM, Guarro J, Sutton D, Starks PT (2012) Mucor nidicola sp. nov., a fungal species isolated from an invasive paper wasp nest. Int J Syst Evol Microbiol 62:1710–1714

    Article  CAS  PubMed  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 Sordariomycetes. Fungal Divers 72:199–301

    Article  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 (2016) Families of Sordariomycetes. Fungal Divers 72:199–301

    Article  Google Scholar 

  • Mains EB (1959a) North American species of Aschersonia parasitic on Aleyrodidae. J Insect Pathol 1:43–47

    Google Scholar 

  • Mains EB (1959b) Species of Aschersonia (Sphaeropsidales). Lloydia 22:215–221

    Google Scholar 

  • Marano AV, Pires-Zottarelli CLA, de Souza JI, Glockling SL, Leaño E, Gachon CMM, Strittmatter M, Gleason FH (2012) Hyphochytriomycota, Oomycota and Perkinsozoa (Supergroup Chromalveolata). In: Jones EBG, Pang KL (orgs.) Marine fungi and fungal-like organisms. De Gruyter, Berlin, pp 167–213

  • Marano AV, Jesus AL, Pires-Zottarelli CLA et al. (2014). Phylogenetic relationships of Pythiales and Peronosporales (Oomycetes, Straminipila) within the “peronosporalean galaxy”. In: Jones EBG, Hyde KD, Pang KL (orgs.) Freshwater Fungi and fungal-like organisms. De Gruyter, Berlin, pp 177–199

  • Marano AV, Jesus AL, de Souza JI, Jerônimo GH, Gonçalves DR, Boro MC, Rocha SCO, Pires-Zottarelli CLA (2016) Ecological roles of saprotrophic Peronosporales (Oomycetes, Straminipila) in natural environments. Fungal Ecol 19:77–88

    Article  Google Scholar 

  • Matheny PB, Curtis JM, Hofstetter V, Aime MC, Moncalvo JM, Ge ZW, Slot JC, Ammirati JF, Baroni TJ, Bougher NL, Hughes KW, Lodge DJ, Kerrigan RW, Seidl MT, Aanen DK, DeNitis M, Daniele GM, Desjardin DE, Kropp BR, Norvell LL, Parker A, Vellinga EC, Vilgalys R, Hibbett DS (2006) Major clades of Agaricales: a multi-locus phylogenetic overview. Mycologia 98:982–995

    Article  PubMed  Google Scholar 

  • Martín MT, Martín L, de-Francisco MT, Cobos R (2009) First report of Lasidiplodia theobromae and Cryptovalsa ampelina associated with grapevine decline from Castillay Leon, Spain. Plant Dis 93:545

    Article  Google Scholar 

  • McNeill J, Barrie FR, Burdet HM, Demoulin V, Hawksworth DL, Marhold K, Nicolson DH, Prado J, Silva PC, Skog JE, Wiersema JH, Turland NJ (eds) (2006) International Code of Botanical Nomenclature (Vienna Code). A. R. G. Gantner Verlag, Ruggell

    Google Scholar 

  • McNeill J, Barrie FR, Buck WR et al (2012) International code of nomenclature for algae, fungi, and plants (Melbourne Code). Regnum Veg 154. Koeltz Botanic Books, Koenigstein

  • Mehrabi M, Mohammadi Goltapeh E, Fotouhifar KB (2011) Studies on Cytospora canker disease of apple trees in Semirom region of Iran. J Agricu Technol 7:967–982

    Google Scholar 

  • Mehrabi M, Hemmati R, Vasilyeva LN, Trouillas FP (2015) A new species and a new record of Diatrypaceae from Iran. Mycosphere 6:60–68

    Article  Google Scholar 

  • Mehrotra BS, Mehrotra BM (1978/1979) Another azygosporic species of Mucor from India. Sydowia 31:94–96

  • Mostert L, Halleen F, Creaser ML, Crous PW (2004) Cryptovalsa ampelina, a forgotten shoot and cane pathogen of grapevines. Austral Pl Pathol 33:295–299

    Article  Google Scholar 

  • 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, McClean TM, Walker JF, Buyck B (2001) A molecular phylogeny of the Russulales including agaricoid, gasteroid and pleurotoid taxa. Mycologia 93:344–354

    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 

  • Miller SL, Aime MC, Henkel TW (2012) Russulaceae of Pakaraima Mountain of Guyana 2. new species of Russula and Lactifluus. Mycotaxon 121:233–253

    Article  Google Scholar 

  • Mirarab S, Nguyen N, Warnow T et al. (2014) PASTA: ultra-large multiple sequence alignment. In: Sharan R (ed) Research in Computational Molecular Biology (RECOMB). Springer International Publishing, Gewerbestrasse

  • Mirza JH, Khan SM, Begum S, Shagufta S (1979) Mucorales of Pakistan. University of Agriculture, Faisalabad

    Google Scholar 

  • Moncalvo JM, Ryvarden L (1997) A nomenclatural study of the Ganodermataceae Donk. Fungi Flora 10:1–114

    Google Scholar 

  • Moncalvo JM, Lutzoni FM, Rehner SA, Johnson J, Vilgalys R (2000) Phylogenetic relationships of agaric fungi based on nuclear large subunit ribosomal DNA sequences. Syst Biol 49:278–305

    Article  CAS  PubMed  Google Scholar 

  • Moncalvo JM, Vilgalys R, Redhead SA, Johnson JE, James TY, Aime MC, Hofstetter V, Verduin SJW, Larsson E, Baroni TJ, Thorn GR, Jacobsson S, Clémençon H, Miller OK (2002) One hundred and seventeen clades of euagarics. Mole Phyl Evol 23:357–400

    Article  CAS  Google Scholar 

  • Müller E, von Arx JA (1962) Die Gattungen der didymosporen Pyrenomyceten. Beiträge. Kryptogamenflora Schweiz 11:1–922

    Google Scholar 

  • Musumeci E (2014) Fungi Non Delineati raro vel haud perspecte et explorate descripti aut definite picti. Pars LXVII–LXIX. Contributo alla conoscenza della Micoflora europea: Specie nuove endemiche, funghi rari con microclima localizzato. Candusso Edizioni, I-Alassio-(SV)

  • Muszewska A, Pawlowska J, Krzys’sciak P (2014) Biology, systematics, and clinical manifestations of Zygomycota infections. Eur J Clin Microbiol Infect Dis 33:1273–1287

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • MycoBank (2016) http://www.mycobank.org/Biolomics.aspx?Table=Mycobank. Accessed on March 2016

  • Naher M, Motohash K, Watanabe H, Chikuo Y, Senda M, Suga H, Brasier C, Kageyama K (2011) Phytophthora chrysanthemi sp. nov., a new species causing root rot of chrysanthemum in Japan. Mycol Prog 10:21–31

    Article  Google Scholar 

  • Nag Raj TR (1993) Coelomycetous anamorphs with appendage-bearing conidia. Mycologue Publications, Waterloo

    Google Scholar 

  • Nakagiri A (2002) Diversity and phylogeny of Halophytophthora (Oomycetes). In: Book of abstracts of the IMC7 – The 7th International Mycological Congress. Oslo, 11–17 Aug 2002. No 55 Book of Abstracts p 19

  • Nakagiri A, Izumi O (2005) Phylogeny, taxonomy and ecology of Halophytophthora spinosa (marine oomycetes). Inoculum 56:43

    Google Scholar 

  • Niemelä T, Wagner T, Fischer M, Dai YC (2001) Phellopilus gen. nov. and its affinities within Phellinus s. lato and Inonotus s. lato (Basidiomycetes). Ann Bot Fenn 38:51–62

    Google Scholar 

  • Nitschke TRJ (1867) Pyrenomycetes Germanici. Die Kernpilze Deutschlands Bearbeitet von Dr. Th. Nitschke. Erster Band. Erste Lieferung i-ii, 156 Germany, Bresalau; Verlag von Eduard Trewendt

  • Norphanphoun C, Maharachchikumbura SSN, Daranagama A, BulgakovTS BDJ, Bahkali AH, Hyde KD (2015) Towards a backbone tree for Seimatosporium, with S. physocarpi sp. nov. Mycosphere 6:385–400

    Google Scholar 

  • O’Donnell K, Cigelnik E, Benny GL (1998) Phylogenetic relationships among the Harpellales and Kickxellales. Mycologia 90:624–639

    Article  Google Scholar 

  • O’Donnell K, Lutzoni FM, Ward TJ, Benny GL (2001) Evolutionary relationships among mucoralean fungi (Zygomycota): evidence for family polyphyly on a large scale. Mycologia 93:286–296

    Article  Google Scholar 

  • Ogawa J, Sakurdani E, Kishino S, Ando A, Yokozeki K, Shimizu S (2012) Polyunsaturated fatty acids production and transformation by Mortierellaalpina and anaerobic bacteria. Eur J Lipid Sci Technol 114:1107–1113

    Article  CAS  Google Scholar 

  • Okane I, Nakagiri A, Ito T (1996) Discostroma tricellulare, a new endophytic ascomycete with a Seimatosporium anamorph isolated from Rhododendron. Can J Bot 74:1338–1344

    Article  Google Scholar 

  • Omvik A (1955) Two new species of Chaetomium and one new Humicola species. Mycologia 47:748–757

    Article  Google Scholar 

  • Orpin CG (1975) Studies on the rumen flagellate Neocallimastix frontalis. J Gen Microbiol 91:249–262

    Article  CAS  PubMed  Google Scholar 

  • Orpin CG (1977a) The occurrence of chitin in the cell walls of the rumen organisms Neocallimastix frontalis, Piromonas communis and Sphaeromonas communis. J Gen Microbiol 99:215–218

    Article  CAS  PubMed  Google Scholar 

  • Orpin CG (1977b) The rumen flagellate Piromonas communis: its life-history and invasion of plant material in the rumen. J Gen Microbiol 99:107–117

    Article  CAS  PubMed  Google Scholar 

  • Orpin CG, Munn EA (1986) Neocallimastix patriciarum sp. nov., a new member of the Neocallimasticaceae inhabiting the rumen of sheep. Trans Br Mycol Soc 86:178–181

    Article  Google Scholar 

  • Ott M, Zola J, Aluru S et al. (2007) Large-scale maximum likelihood-based phylogenetic analysis on the IBM BlueGene/L. Proceedings of ACM/IEEE Supercomputing conference. Article No. 4

  • Pang KL, Vrijmoed LLP, Kong RYC, Jones EBG (2003) Lignincola and Nais, polyphyletic genera of the Halosphaeriales (Ascomycota). Mycol Prog 2:29–36

    Article  Google Scholar 

  • Pang KL, Lin HJ, Lin HY, Huang YF, Chen YM (2015) Production of arachidonic and eicosapentaenoic acids by the marine oomycete Halophytophthora. Mar Biotechnol 17:121–129

    Article  CAS  PubMed  Google Scholar 

  • Parra LA (2008) Agaricus L Allopsalliota Nauta & Bas. Pars 1Edizioni Candusso Alassio, Italy

    Google Scholar 

  • Parra LA (2013) Fungi Europaei, volume 1A, Agaricus L.:Allopsalliota, Nauta & Bas (Parte II). Candusso Edizioni, Alassio Italy

  • Pegler DN (1983) The genus Lentinus: a world monograph. HMSO, London

    Google Scholar 

  • Pegler DN (1985) The genus Clarkeinda (Basidiomycotina: Agaricaceae). Bot J Linn Soc 91:245–252

    Article  Google Scholar 

  • Pegler DN (1986) Agaric flora of Sri Lanka. Kew Bull. Additional Series 6, Her Majesty’s Stationary Office, London

  • Pei KQ (2000) A new variety of Mucor variosporus and the validation of M. luteus Linnemann and M. variosporus Schipper. Mycosystema 19:10–12

    CAS  Google Scholar 

  • Peintner U, Bougher NL, Castellano MA, Moncalvo JM, Moser MM, Trappe JM, Vilgalys R (2001) Multiple origins of sequestrate fungi related to Cortinarius (Cortinariaceae). Am J Bot 88:2168–2179

    Article  CAS  PubMed  Google Scholar 

  • Peintner U, Horak E, Moser M, Vilgalys R (2002) Phylogeny of Rozites, Cuphocybe and Rapacea inferred from ITS and LSU rDNA sequences. Mycologia 94:620–629

    Article  CAS  PubMed  Google Scholar 

  • Petch T (1921) Studies in entomogenous fungi. II. The genera of Hypocrella and Aschersonia. Ann Roy Bot Gard Perad 7:167–278

    Google Scholar 

  • Petch T (1931) Notes on entomogenous fungi. Trans Brit Mycol Soc 16:55–75

    Article  Google Scholar 

  • Petch T (1932) A list of the entomogenous fungi of Great Britain. Trans Brit Mycol Soc 17:170–178

    Article  Google Scholar 

  • Petch T, Bisby GR (1950) The fungi of ceylon. Peradeniya Manual 6:111pp

  • Petrak F (1923a) Mykologische Notizen VI. No. 226. Über die Gattung Glonium Muhl. Ann Mycol 21:225–227

    Google Scholar 

  • Petrak F (1923b) Mykologische Notizen VI, Nr. 284. Psiloglonium finkii nov. sp. Annal Mycol 21:308–309

    Google Scholar 

  • Petrak F (1934) Mykologische Notizen. XII. Annal Mycol 32:317–447

    Google Scholar 

  • Petrak F (1941) Mykologische Notizen. XIV. Annal Mycol 39:251–349

    Google Scholar 

  • Paterson RRM (2006) Ganoderma – a therapeutic fungal bio factory. Photochemistry 67:1985–2001

    Article  CAS  Google Scholar 

  • Petrini LE (1992) Rosellinia species of the temperate zones. Sydowia 44:169–281

    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 

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

    Google Scholar 

  • Pilotti CA, Sanderson FR, Aitken AB, Armstrong W (2004) Morphological variation and host range of two Ganoderma species from Papua New Guinea. Mycopathologia 158:251–265

    Article  PubMed  Google Scholar 

  • Pinnoi A, Phongpaichit P, Jeewon R, Tang AMC, Hyde KD, Jones EBG (2010) Phylogenetic relationships of Astrocystis eleiodoxae sp. nov. (Xylariaceae). Mycosphere 1:1–9

    Google Scholar 

  • Phillips A, Alves A, Correia A, Luque J (2005) Two new species of Botryosphaeria with brown, 1-septate ascospores and Dothiorella anamorphs. Mycologia 97:513–529

    Article  PubMed  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 PEXJC, 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 

  • Pitt WM, Trouillas FP, Gubler WD, Savocchia S, Sosnowski MR (2013a) Pathogenicity of diatrypaceous fungi on grapevines in Australia. Plant Dis 97:749–756

    Article  Google Scholar 

  • Pitt WM, Úrbez-Torres JR, Trouillas FP (2013b) Dothiorella vidmadera, a novel species from grapevines in Australia and notes on Spencermartinsia. Fungal Divers 61:209–219

    Article  Google Scholar 

  • Pitt WM, Úrbez-Torres JR, Trouillas FP (2015) Dothiorella and Spencermartinsia, new species and records from grapevines in Australia. Aust Pl Pathol 44:43–56

    Article  Google Scholar 

  • Quaedvlieg W, Kema GHJ, Groenewald JZ, Verkley GJM, Seifbarghi S, Razavi M, Mirzadi Gohari A, Mehrabi R, Crous PW (2011) Zymoseptoria gen. nov.: a new genus to accommodate Septoria- like speciesoccurring on graminicolous hosts. Persoonia 26:57–69

    Article  CAS  PubMed  PubMed Central  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 

  • Quandt CA, Kepler RM, Gams W, Araújo JP, Ban S, Evans HC, Luangsa-Ard JJ (2014) Phylogenetic-based nomenclatural proposals for Ophiocordycipitaceae (Hypocreales) with new combinations in Tolypocladium. IMA Fungus 5:121

    Article  PubMed  PubMed Central  Google Scholar 

  • Raja HA, Shearer CA (2008) Freshwater ascomycetes: new and noteworthy species from aquatic habitats in Florida. Mycologia 100:467–489

    Article  PubMed  Google Scholar 

  • Raja HA, Tanaka K, Hirayama K, Miller AH, Shearer CA (2011) Freshwater ascomycetes: two new species of Lindgomyces (Lindgomycetaceae, Pleosporales, Dothideomycetes) from Japan and USA. Mycologia 103:1421–1432

    Article  PubMed  Google Scholar 

  • Raja HA, Oberlies NH, El-Elimat T, Miller AN, Zelski SE, Shearer CA (2013) Lindgomyces angustiascus (Lindgomycetaceae, Pleosporales, Dothideomycetes), a new lignicolous species from freshwater habitats in the USA. Mycoscience 54:353–361

    Article  CAS  Google Scholar 

  • Rajchenberg M, Pildain MB, Bianchinotti MV, Barroetaveña C (2015) The phylogenetic position of poroid Hymenochaetaceae (Hymenochaetales, Basidiomycota) from Patagonia, Argentina. Mycologia 107:754–767

    Article  CAS  PubMed  Google Scholar 

  • Rea AJ, Burgess TI, Hardy GESJ, Stukely MJC, Jung T (2011) Two novel and potentially endemic species of Phytophthora associated with episodic dieback of Kwongan vegetation in the south-west of Western Australia. Plant Pathol 60:1055–1068

    Article  Google Scholar 

  • Réblová M, Winka K (2000) Phylogeny of Chaetosphaeria and its anamorphs based on morphological and molecular data. Mycologia 92:939–954

    Article  Google Scholar 

  • Réblová M, Barr ME, Samuels GJ (1999) Chaetosphaeriaceae, a new family for Chaetosphaeria and its relatives. Sydowia 51:49–70

    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 

  • Reeser PW, Sutton W, Hansen EM, Remigi P, Adams GC (2011) Phytophthora species in forest streams in Oregon and Alaska. Mycologia 103:22–35

    Article  PubMed  Google Scholar 

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

    Google Scholar 

  • Ribes JA, Vanover-Sams CL, Baker DJ (2000) Zygomycetes in human disease. Clin Microbiol Rev 13:236–301

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ridgway R (1912) Colour standards and colour nomenclature. Robert Ridgway, Washington

    Google Scholar 

  • Rivas Plata E, Lücking R, Lumbsch HT (2008) When family matters: an analysis of Thelotremataceae (Lichenized Ascomycota: Ostropales) as bioindicators of ecological continuity in tropical forests. Biodiv Cons 17:1319–1351

    Article  Google Scholar 

  • Rivas Plata E, Lumbsch HT, Lücking R (2012a) A new classification for the lichen family Graphidaceae s.lat. (Ascomycota: Lecanoromycetes: Ostropales). Fung Divers 52:107–121

    Article  Google Scholar 

  • Rivas Plata E, Lücking R, Lumbsch HT (2012b) Molecular phylogeny and systematics of the Ocellularia-clade (Ascomycota: Ostropales: Graphidaceae). Taxon 61:1161–1179

    Google Scholar 

  • Rivas PE, Parnmen S, Staiger B, Mangold A, Frisch A, Weerakoon G, Hernández JE, Cáceres MES, Kalb K, Sipman HJM, Common RS, Nelsen MP, Lücking R, Lumbsch HT (2013) A molecular phylogeny of Graphidaceae (Ascomycota: Lecanoromycetes: Ostropales) including 428 species. MycoKeys 6:55–94

    Article  Google Scholar 

  • Roa Engel CA, Straathof AJJ, Zijlmans TW, van Gulik WM, van der Wielen LAM (2008) Fumaric acid production by fermentation. App Microbiol Biotech 78:379–389

    Article  CAS  Google Scholar 

  • Robideau GP, de Cock AWAM, Coffey MD, Voglmayr H, Brouwer H, Bala K, Chitty DW, Désaulniers N, Eggertson QA, Gachon CMM, Hu CH, Küpper FC, Rintoul TL, Sarhan E, Verstappen ECP, Zhang Y, Bonants PJM, Ristaino JB, Lévesque AC (2011) DNA barcoding of oomycetes with cytochrome c oxidase subunit I and internal transcribed spacer. Mol Ecol Resour 11:1002–1011

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Rogers JD (2000) Thoughts and musings about tropical Xylariaceae. Mycol Res 104:1412–1420

    Article  Google Scholar 

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

    Google Scholar 

  • Romagnesi H (1985) Les Russules d’ Europe et d’ Afrique du Nord. Reprint with supplement. J. Cramer, Lehre

  • Romagnesi H (1987) Status et noms nouveaux pour les taxa infragénériques dans le genere Russula. Document Mycologique 18:39–40

    Google Scholar 

  • Ronquist F, Teslenko M, Van Der Mark P, Ayres DL, Darling A, Hohna 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. Sist Biol 61:1–4

    Article  Google Scholar 

  • Rossman AY, Palm ME (2006) Why are Phytophthora and other Oomycota not true Fungi? Outlook Pest Manag 17:217–219

    Article  Google Scholar 

  • Rossman AY, Samuels GJ, Rogerson CT, Lowen R (1999) Genera of Bionectriaceae, Hypocreaceae and Nectriaceae (Hypocreales, Ascomycetes). Stud Mycol 42:1–248

    Google Scholar 

  • Rossman AY, McKemy JM, Pardo-Schultheiss RA, Schroers HJ (2001) Molecular studies of the Bionectriaceae using large subunit rDNA sequences. Mycologia 93:100–110

    Article  CAS  Google Scholar 

  • Rossman AY, Adams GC, Cannon PF, Castlebury LA, Crous PW, Gryzenhout M, Jaklitsch WM, Mejia LC, Stoykov D, Udayanga D, Voglmayr H, Walker DM (2015) Recommendations of generic names in Diaporthales competing for protection or use. IMA Fungus 6:145–154

    Article  PubMed  PubMed Central  Google Scholar 

  • Ryvarden L (1991) Genera of polypores, nomenclature and taxonomy. Fungiflora, Oslo

    Google Scholar 

  • Ryvarden L (2005) The genus Inonotus, a synopsis. Synopsis Fungorum 21:1–149

    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) Sylloge Fungorum 1: i-xviii. Italy, Padua, pp 187–188

  • Saccardo PA (1884) Sylloge fungorum vol 3. Typis Seminarii, Italy (in Latin)

    Google Scholar 

  • Sakayaroj J, Pang KL, Jones EBG (2011) Multi-gene phylogeny of the Halosphaeriaceae: its ordinal status, relationships between genera and morphological character evolution. Fungal Divers 46:87–109

    Article  Google Scholar 

  • Samuels GJ, Candoussau F, Magni JF (1997) Fungicolous pyrenomycetes 1. Helminthosphaeria and the new family Helminthosphaeriaceae. Mycologia 89:141–155

    Article  Google Scholar 

  • Sánchez-García M, Matheny PB, Palfner G, Lodge DJ (2014) Deconstructing the Tricholomataceae (Agaricales) and introduction of the new genera Albomagister, Corneriella, Pogonoloma and Pseudotricholoma. Taxon 63:993–1007

    Article  Google Scholar 

  • Santiago ALCMA, Santos PJP, Trufem SFB, Malosso E, Cavalcanti MAQ (2011) Zygomycetes from herbivore dung in the Ecological Reserve of Dois Irmãos, Northeast Brazil. Braz J Microbiol 42:89–95

    Article  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 

  • Santos MJS, de Oliveira PC, Trufem SFB (2003) Morphological observations on Absidia corymbifera and Absidia blakesleeana strains perserved under mineral oil. Mycoses 46:402–406

    Article  PubMed  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 

  • Sato G, Tanaka K, Hosoya T (2008) Bambusicolous fungi in Japan (8): a new species of Pseudolachnella from Yakushima Island, southern Japan. Mycoscience 49:392–394

    Article  Google Scholar 

  • Schardl CL, Young CA, Moore N et al. (2014) Chapter ten – genomes of plant-associated Clavicipitaceae. In: Advances in botanical research. Martin FM (ed). INRA Centre de Nancy, Centre de Nancy, Champenoux. Academic Press Inc, pp 291–327

  • Schipper MAA (1973) A study on variability in Mucor hiemalis and related species. Stud Mycol 4:1–40

    Google Scholar 

  • Schipper MAA (1975) Mucor mucedo, Mucor flavus and related species. Stud Mycol 10:1–33

    Google Scholar 

  • Schipper MAA (1976) On Mucor circinelloides, Mucor racemosus and related species. Stud Mycol 12:1–40

    Google Scholar 

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

    Google Scholar 

  • Schipper MAA (1984) A revision of the genus Rhizopus I. the Rh. stolonifer-group and Rh. oyzae. Stud Mycol 25:1–19

    Google Scholar 

  • Schipper MAA, Stalpers JA (1984) A revision of the genus Rhizopus II. the Rh. microsporus-group. Stud Mycol 25:20–34

    Google Scholar 

  • Schipper MAA (1990) Note on Mucorales-I. observations on Absidia. Persoonia 14:133–149

    Google Scholar 

  • Schipper MAA, Samson RA (1994) Miscellaneous notes on Mucoraceae. Mycotaxon 50:475–491

    Google Scholar 

  • Schoenlein-Crusius IH, Milanez AI, Trufem SFB, Pires-Zottarelli CLA, Grandi RAP, Santos ML, Giustra KC (2006) Microscopic fungi in the Atlantic Rainforest in Cubatão, São Paulo, Brazil. Braz J Microbiol 37:267–275

    Article  Google Scholar 

  • Seguy E (1936) Code universel des couleurs. P. Lechevalier, Paris

    Google Scholar 

  • Senanayake IC, Maharachchikumbura SSN, Hyde KD, Bhat DJ, 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 

  • Sharma JR (1995) Hymenochaetaceae of India. Botanical Survey of India, Calcutta

    Google Scholar 

  • Sharma S, Chadha BS, Kaur M, Ghatora SK, Saini HS (2008) Molecular characterization of multiple xylanase producing thermophilic/thermotolerant fungi isolated from composting materials. Let Appl Microbiol 46:526–535

    Article  CAS  Google Scholar 

  • Shearer CA (1989) Aniptodera (Halosphaeriaceae) from wood in freshwater habitats. Mycologia 81:139–146

    Article  Google Scholar 

  • Shearer CA, Miller M (1977) Fungi of the Chesapeake Bay and its tributaries V. Aniptodera chesapeakensis gen. et sp. nov. Mycologia 69:887–897

    Article  Google Scholar 

  • Shoemaker RA (1964) Seimatosporium (= Cryptostictis) parasites of Rosa, Vitis, and Cornus. Can J Bot 42:411–417

    Article  Google Scholar 

  • Shoemaker RA, Muller E (1964) Generic correlations and concepts: Clathridium (= Griphosphaeria) and Seimatosporium (= Sporocadus). Can J Bot 42:403–407

    Article  Google Scholar 

  • Silvestro D, Michalak I (2011) RaxmlGUI: a graphical front-end for RAxML. Org Divers Evol 12:335–337

    Article  Google Scholar 

  • Singer R (1940) Notes sur quelques Basidiomycètes. Rev Mycol 5:3–13

    Google Scholar 

  • Singer R (1947) The Boletoideae of Florida. the Boletineae of Florida with notes on extralimital species III. Am Midl Nat 37:1–135

    Article  Google Scholar 

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

    Google Scholar 

  • Singh SK, Doshi A, Pancholy A, Pathak R (2013) Biodiversity in wood–decay macro–fungi associated with declining arid zone trees of India as revealed by nuclear rDNA analysis. Eur J Plant Pathol 136:373–382

    Article  CAS  Google Scholar 

  • Singtripopa C, Camporesi E, Ariyawansa HA, Wanasinghe DN, Bahkali AH, Chomnunti P, Boonmee S, Hyde KD (2015) Keissleriella dactylidis, sp. nov., from Dactylis glomerata and its phylogenetic placement. Sci Asia 41:295–304

    Article  Google Scholar 

  • Sir EB, Kuhnert E, Lambert C, Hladki AI, Romero AI, Stadler M (2016) New species and reports of Hypoxylon from Argentina recognized by a polyphasic approach. Mycol Prog. doi:10.1007/s11557-016-1182-z

    Google Scholar 

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

    Google Scholar 

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

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Slippers B, Roux J, Wingfield MJ, van der Walt FJJ, Jami F, Mehl JWM, Marais GJ (2014) Confronting the constraints of morphological taxonomy in the Botryosphaeriales. Persoonia 33:55–168

    Article  Google Scholar 

  • Smith AH, Thiers HD (1971) The Boletes of Michigan. University of Michigan Press, Ann Arbor

    Google Scholar 

  • Smith JDG, Liew ECY, Hyde KD (2001) The Xylariales: a monophyletic order containing 7 families. Fungal Divers 13:175–208

    Google Scholar 

  • Smith ME, Gryganskyi A, Bonito G, Nouhra E, Moreno-Arroyo B, Benny G (2013) Phylogenetic analysis of the genus Modicella reveals an independent evolutionary origin of sporocarp-forming fungi in the Mortierellales. Fung Gen Biol 61:61–68

    Article  Google Scholar 

  • Sogonov MV, Castlebury LA, Rossman AY, Mejía LC, White JF Jr (2008) Leaf-inhabiting genera of the Gnomoniaceae, Diaporthales. Stud Mycol 62:1–79

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Somrithipol S, Sakayaroj J, Rungjindamai N, Plaingam N, Jones EBG (2008) Phylogenetic relationship of the coelomycete genus Infundibulomyces based on nuclear rDNA data. Mycologia 100:735–741

    Article  PubMed  Google Scholar 

  • Song J, Chen Y, Cui B, Liu H, Wang Y (2014) Morphological and molecular evidence for two new species of Laetiporus (Basidiomycota, Polyporales) from southwestern China. Mycologia 106:1039–1050

    Article  PubMed  Google Scholar 

  • Spatafora JW, Quandt CA, Kepler RM, Sung GH, Shrestha B, Hywel-Jones NL, Luangsa-ard JJ (2015) New 1F1N species Combinations in Ophiocordycipitaceae (Hypocreales). IMA Fungus 6:357–362

    Article  PubMed  PubMed Central  Google Scholar 

  • Spatafora JW, Sung GH, Sung JM, Hywel-Jones NL, White JF (2007) Phylogenetic evidence for an animal pathogen origin of ergot and the grass endophytes. Mol Ecol 16:1701–1711

    Article  CAS  PubMed  Google Scholar 

  • Spielman LJ (1983) Taxonomy and Biology of Valsa Species on Hardwoods in North America, with special reference to species on maples. Cornell University, NY

    Google Scholar 

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

    Article  Google Scholar 

  • Spooner BM (1981) New records and species of British microfungi. Trans Brit Mycol Soc 76:265–301

    Article  Google Scholar 

  • Stadler M (2011) Importance of secondary metabolites in the Xylariaceae as parameters for assessment of their taxonomy, phylogeny, and functional biodiversity. Curr Res Environ Appl Mycol 1:75–133

    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 30:1312–1313

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Stamatakis A, Hoover P, Rougemont J (2008) A rapid bootstrap algorithm for the RAxML web servers. Syst Biol 57:758–777

    Article  PubMed  Google Scholar 

  • Stubbe D, Nuytinck J, Verbeken A (2010) Critical assessment of the Lactarius gerardii species complex (Russulales). Fungal Biol 114:271–283

    Article  CAS  PubMed  Google Scholar 

  • Su HY, Hyde KD, Maharachchikumbura SSN, Ariyawansa HA, Luo ZL, Promputtha I, Tian Q, Lin CG, Shang QJ, Zhao YC, Chai HM, Liu XY, Bahkali AH, Bhat JD, McKenzie EHC, Zhou DQ (2016) The families Distoseptisporaceae fam. nov., Kirschsteiniotheliaceae, Sporormiaceae and Torulaceae, with new species from freshwater in Yunnan Province, China. Fingal Divers. doi:10.1007/s13225-016-0362-0

    Google Scholar 

  • Subrahamanyam A (1983) Studies on themomycology. Mucor thermo-hyalospora sp. nov. Bibl Mycol 91:421–423

    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 GH, Hywel-Jones NL, Sung JM, 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 

  • Šutara J (2008) Xerocomus s.l. in the light of the present state of knowledge. Czech Mycol 60:29–62

    Google Scholar 

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

    Google Scholar 

  • Swofford DL (2002) PAUP: phylogenetic analysis using parsimony, version 4.0b10. Illinois Natural History Survey, Champion, III

  • Tadych M, Chaverri P, Bergen M, White JF (2009) Moelleriella zhongdongii: stroma development and identification of hirsutella-like and Aschersonia synanamorphs. Mycol Res 113:611–615

    Article  PubMed  PubMed Central  Google Scholar 

  • Tanabe Y, Saikawa M, Watanabe MM, Sugiyama J (2003) Molecular phylogeny of Zygomycota based on EF-1alpha and RPB1 sequences: limitations and utility of alternative markers to rDNA. Mol Phylogenet Evol 30:438–449

    Article  CAS  Google Scholar 

  • Tanaka K, Harada Y (2003) Pleosporales in Japan (2): the genus Lophiotrema. Mycoscience 44:115–121

    Article  Google Scholar 

  • Tanaka K, Hirayama K, Yonezawa H, Hatakeyama S, Harada Y, Sano T, Shirouzu T, Hosoya T (2009) Molecular taxonomy of bambusicolous fungi: Tetraplosphaeriaceae, a new pleosporalean family with Tetraploa-like anamorphs. Stud Mycol 64:175–209

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tanaka K, Endo M, Hirayama K, Okane I, Hosoya T, Sato T (2011) Phylogeny of Discosia and Seimatosporium, and introduction of Adisciso and Immersidiscosia genera nova. Persoonia 26:85–98

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Tang LP, Hao YJ, Cai Q, Tolgor B, Yang ZL (2014) Morphological and molecular evidence for a new species of Rhodotus from tropical and subtropical Yunnan, China. Mycol Progr 13:45–53

    Article  Google Scholar 

  • Teng SC (1936) Additional fungi from China IV. Sinensia 7:752–823

    Google Scholar 

  • Teunissen MJ, Op den Camp HJ, Orpin CG, Huis in’t Veld JH, Vogels GD (1991) Comparison of growth characteristics of anaerobic fungi isolated from ruminant and non-ruminant herbivores during cultivation in a defined medium. J Gen Microbiol 137:1401–1408

    Article  CAS  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, Ariyawansa HA, Liu ZY, Chukeatirote E, Hyde KD (2014c) Towards a natural classification of Dothideomycetes 6: the genera Dolabra, Placostromella, Pleosphaerellula, Polysporidiella and Pseudotrichia (Dothideomycetes incertae sedis). Phytotaxa 176:55–67

    Article  Google Scholar 

  • Thambugala KM, Hyde KD, Eungwanichayapant PD, Romero AI, Liu ZY (2016) Additions to the genus Rhytidhysteron in Hysteriaceae. Cryptogam Mycol 37:99–116

  • 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 

  • Theissen F, Sydow H (1917) Synoptische Tafeln. Ann Mycol 15:389–491

    Google Scholar 

  • Tian Q, Hyde KD, Liu JK, Wanasinghe DN, Boonmee S, Senanayak IC, Luo ZL, Ariyawansa H, Li WJ, Thambugala KM, Jones EBG, Bhat DJ, Bahkali AH, Chomnunti P, Mortimer PE, Xu JC, Campesori E (2015) Phylogenetic relationships and morphological reappraisal of Melanommataceae. Fungal Divers 74:267–324

    Article  Google Scholar 

  • Traaen AE (1914) Untersuchungen über Bodenpilze aus Norwegen. Nytt Mag Naturvidenskapene 52:1–121

    Google Scholar 

  • Trakunyingcharoen T, Lombard L, Groenewald JZ, Cheewangkoon R, Toanun C, Alfenas AC, Crous PW (2014) Mycoparasitic species of Sphaerellopsis, and allied lichenicolous and other genera. IMA Fungus 5:391–414

    Article  PubMed  PubMed Central  Google Scholar 

  • Trouillas FP, Úrbez-Torres JR, Gubler WD (2010) Diversity of diatrypaceous fungi associated with grapevine canker diseases in California. Mycologia 102:319–336

    Article  CAS  PubMed  Google Scholar 

  • Trouillas FP, Pitt WM, Sosnowski MR, Huang R, Peduto F, Loschiavo A, Savocchia S, Scott ES, Gubler WD (2011) Taxonomy and DNA phylogeny of Diatrypaceae associated with Vitis vinifera and other woody plants in Australia. Fungal Divers 49:203–223

    Article  Google Scholar 

  • Tuckwell DS, Nicholson MJ, McSweeney CS, Theodorou MK, Brookman JL (2005) The rapid assignment of ruminal fungi to presumptive genera using ITS1 and ITS2 RNA secondary structures to produce group-specific fingerprints. Microbiology 151:1557–1567

    Article  CAS  PubMed  Google Scholar 

  • Tulasne LR, Tulasne C (1861) Selecta Fungorum Carpologia: Erysiphei Vol 1. Imperial Press, Paris

  • Tulloss RE, Yang ZL (2016) Amanitaceae studies. http://www.amanitaceae.org

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

    Google Scholar 

  • Van de Putte K, Nuytinck J, Stubbe D, Huyen TL, Verbeken A (2010) Lactarius volemus sensu lato (Russulales) from northern Thailand: morphological and phylogenetic species concepts explored. Fungal Divers 45:99–130

    Article  Google Scholar 

  • van Tieghem P (1876) Sur le développement du fruit des Ascodesmis, genre nouveau de l’ordre des Ascomycètes. Bull Soc Bot Fr 23:271–279

    Article  Google Scholar 

  • Vasilyeva LN, Stephenson SL (2005) Pyrenomycetes of the Great Smoky Mountains National Park. II. Cryptovalsa Ces. et De Not. and Diatrypella (Ces. et De Not.) Nitschke (Diatrypaceae). Fungal Divers 19:189–200

    Google Scholar 

  • Vasilyeva LN, Mel’nik VA (2006) New pyrenomycetous species from Korea and South Africa. Mikol Fitopatol 40:89–92

    Google Scholar 

  • Vavra J, Joyon L (1966) Étude sur la morphologie, le cycle évolutif et la position systematique de Callimastix cyclopsis Weissenberg 1912. Protistologica 2:15–16

    Google Scholar 

  • Vizzini A (2014) Nomenclatural novelties. Index Fungorum 176:1

    Google Scholar 

  • Vizzini A, Contu M, Ercole E (2011) Musumecia gen. nov. in the Tricholomatoid clade (Basidiomycota, Agaricales) related to Pseudoclitocybe. Nord J Bot 29:734–740

    Article  Google Scholar 

  • Vizzini A, Consiglio G, Ercole E, Setti L (2016) Pseudoporpoloma, a new genus for Agaricus pes-caprae (Agaricales, Tricholomataceae). Phytotaxa 243:271–280

    Article  Google Scholar 

  • Vlasák J, Kout J (2011) Pileate Fomitiporia species in the USA. new combinations Fomitiporia calkinsii and F. bakeri. Mycol Prog 10:445–452

    Article  Google Scholar 

  • Vlasák J, Li HJ, Zhou LW, Dai YC (2013) A further study on Inonotus linteus complex (Hymenochaetales, Basidiomycota) in tropical America. Phytotaxa 124:25–36

    Article  Google Scholar 

  • Wagner T, Fischer M (2002) Proceedings towards a natural classification of theworldwide taxa Phellinus s.l. and Inonotus s.l., and phylogenetic relationships of allied genera. Mycologia 94:998–1016

    Article  PubMed  Google Scholar 

  • Wagner L, Stielow B, Hoffmann K, Petkovits T, Papp T, Vágvölgyi C, de Hoog GS, Verkley G, Voigt K (2013) A comprehensive molecular phylogeny of the Mortierellales (Mortierellomycotina) based on nuclear ribosomal DNA. Persoonia 30:77–93

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Walther G, Pawłowska J, Alastruey-Izquierdo A, Wrzosek M, 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 

  • 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 et al. (2016) Taxonomy and phylogeny of Laburnicola gen. nov. (Didymosphaeriaceae, Massarinae). Fungal Biol (in press)

  • Wang DM, Wu SH, Li TH (2009a) Two records of Ganoderma new to mainland China. Mycotaxon 108:35–40

    Article  Google Scholar 

  • Wang J, Zhou W, Yuan H, Wang Y (2008) Characterization of a novel fungal chitosanase Csn2 from Gongronella sp. JG. Carbohydr Res 343:2583–2588

    Article  CAS  PubMed  Google Scholar 

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

    Article  Google Scholar 

  • Wang YW, Hong TW, Tai YL et al. (2015a) Evaluation of an epitypified Ophiocordyceps formosana (Cordycepss.l.) for its pharmacological potential. Evid Based Complement Alternat Med 2015:13

  • Wang ZR, Parra L, Callac P, Zhou JL, Fu WJ, Dui SH, Hyde KD, Zhao RL (2015a) Edible species of Agaricus (Agaricaceae) from Xinjiang Province (Western China). Phytotaxa 202:185–197

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Webb J, Theodorou MK (1991) Neocallimastix hurleyensis sp. nov., an anaerobic fungus from the ovine rumen. Can J Bot 69:1220–1224

    Article  Google Scholar 

  • Weerakoon G (2015) Fascinating Lichens of Sri Lanka. Dilmah Conservation, Colombo

    Google Scholar 

  • Weerakoon G, Aptroot A (2013) Some new lichen species from Sri Lanka, with a key to the genus Heterodermia in Sri Lanka. Cryptogam Mycol 34:321–328

    Article  Google Scholar 

  • Weerakoon G, Aptroot A (2014) Over 200 new lichen records from Sri Lanka, with three new species to science. Cryptogamie Mycol 35:51–62

    Article  Google Scholar 

  • Weerakoon G, Aptroot A, Lumbsch HT, Wolseley PA, Wijeyaratne SC, Gueidan C (2012a) New molecular data on Pyrenulaceae from Sri Lanka reveal two well-supported groups within this family. Lichenologist 44:639–647

    Article  Google Scholar 

  • Weerakoon G, Rivas Plata E, Lumbsch HT, Lücking R (2012b) Three new species of Chapsa (lichenized Ascomycota: Ostropales: Graphidaceae) from tropical Asia. Lichenologist 44:373–379

    Article  Google Scholar 

  • Weerakoon G, Wijeyaratne SC, Wolseley PA, Rivas Plata E, Lücking R, Lumbsch HT (2012c) Six new species of Graphidaceae from Sri Lanka. Bryologist 115:74–83

    Article  Google Scholar 

  • Weerakoon G, Lücking R, Lumbsch HT (2014) Thirteen new species of Graphidaceae (lichenized Ascomycota: Ostropales) from Sri Lanka. Phytotaxa 189:331–347

    Article  Google Scholar 

  • Weerakoon G, Jayalal U, Wijesundara S, Karunaratne V, Lücking R (2015) Six new Graphidaceae (lichenized Ascomycota: Ostropales) from Horton Plains National Park, Sri Lanka. Nova Hedwigia 101:77–88

    Article  Google Scholar 

  • Wehmeyer LE (1957) The genus Saccothecium, Pringsheimia, Pleosphaerulina and Pseudoplea. Mycologia 49:83–94

    Article  Google Scholar 

  • Wei F, Hong Y, Liu J, Yuan J, Fang W, Peng H, Xiao Y (2010) Gongronella sp. induces overproduction of laccase in Panus rudis. J Basic Microbiol 50:98–103

    Article  CAS  PubMed  Google Scholar 

  • Wen TC, Zhu RC, Kang JC, Huang MH, Tan DB, Ariyawansha H, Liu H (2013) Ophiocordyceps xuefengensis sp. nov. from larvae of Phassusnodus (Hepialidae) in Hunan Province, southern China. Phytotaxa 123:41–50

    Article  Google Scholar 

  • Westendorp GD (1857) Sur quelques hypoxylées inédites ou nouvelles pour la flore de la Belgique. Bull de l’Académie Royale de Belgique Classe de Sci, Sér 22:554–579

    Google Scholar 

  • Wicklow DT, Joshi BK, Gamble WR, Gloer JB, Dowd PF (1998) Antifungal metabolites (monorden, monocillin IV, and cerebrosides) from Humicola fuscoatra Traaen NRRL 22980, a mycoparasite of Aspergillus flavus sclerotia. Appl Environ Microbiol 64:4482–4484

    CAS  PubMed  PubMed Central  Google Scholar 

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

    Article  Google Scholar 

  • Wijayawardene NN, Hyde KD, Bhat DJ, Camporesi E, Schumacher RK, Chethana KT, Wikee S, Bahkali AH, Wang Y (2014a) 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, Crous PW, Kirk PM, Hawksworth DL, Boonmee S, Braun U, Chomnunti P, Dai DQ, D’Souza MJ, Diederich P, Dissanayake A, Doilom M, Hongsanan S, Jones EBG, Groenewald JZ, Ayawardena R, Lawrey JD, Liu JK, Lucking R, Madrid H, Manamgoda DS, Muggia L, Nelsen MP, Phookamsak R, Suetrong S, Tanaka K, Thambugala KM, Wikee S, Zhang Y, Aptroot A, Ariyawansa HA, Bahkali AH, Bhat JD, Gueidan C, DeHoog GS, Knudsen K, Mckenzie EHC, Miller AN, Mortimer PE, Wanasinghe DN, Phillips AJL, Raja HA, Slippers B, Shivas RS, Taylor JE, Wang Y, Woudenberg JHC, Piatek M, Cai L, Jaklitsch WM, Hyde KD (2014b) Naming and outline of Dothideomycetes–2014. Fungal Divers 69:1–55

    Article  Google Scholar 

  • Wilson AW, Desjardin DE (2005) Phylogenetic relationships in the gymnopoid and marasmioid fungi (Basidiomycetes, euagarics clade). Mycologia 97:667–679

    Article  CAS  PubMed  Google Scholar 

  • Wingfield MJ, De Beer ZW, Slippers B, Wingfield BD, Groenewald JZ, Lombard L, Crous PW (2012) One fungus, one name promotes progressive plant pathology. Mol Plant Pathol 13:604–613

    Article  CAS  PubMed  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 1:570pp

  • Whalley AJS, Jones EBG, Hyde KD, Læssøe T (1999) Halorosellinia gen. nov. to accommodate Hypoxylon oceanicum, a common mangrove species. Mycol Res 104:368–374

    Article  Google Scholar 

  • White WL, Downing MH (1953) Humicola grisea, a soil-inhabiting, cellulolytic hyphomycete. Mycologia 45:951–963

    Google Scholar 

  • White MM, James TY, O’Donnell K, Cafaro MJ, Tanabe Y, Sugiyama J (2006) Phylogeny of the Zygomycota based on nuclear ribosomal sequence data. Mycologia 98:872–884

    Article  PubMed  Google Scholar 

  • Wu G, Feng B, Xu J, Zhu XT, Li YC, Zeng NK, Hosen MI, 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 

  • Wu SH, Dai YC, Hattori T, Yu TW, Wang DM, Parmasto E, Chang HY, Shih SY (2012) Species clarification for the medicinally valuable ‘sanghuang’ mushroom. Bot Stud 53:135–149

    Google Scholar 

  • Yan JY, Xie Y, Zhang W, Wang Y, Liu JK, Hyde KD, Seem RC, Zhang GC, Wang ZY, Yao SW, Bai XJ, Dissanayake AJ, Peng YL, Li XH (2013) Species of Botryosphaeriaceae involved in grapevine dieback in China. Fungal Divers 61:221–236

    Article  Google Scholar 

  • Yang Q, Fan ZL, Crous PW, Liang YM, Tian CM (2015a) Cytospora from Ulmus pumila in Northern China. Mycol Prog 14:74–85

    Article  Google Scholar 

  • Yang X, Copes WE, Hong C (2014a) Two novel species representing a new clade and cluster of Phytophthora. Fungal Biol 118:72–82

    Article  CAS  PubMed  Google Scholar 

  • Yang X, Gallegly ME, Hong CX (2014b) A high-temperature tolerant species in clade 9 of the genus Phytophthora: P. hydrogena sp. nov. Mycologia 106:57–65

    Article  PubMed  Google Scholar 

  • Yang X, Hong CX (2013) Phytophthora virginiana sp. nov., a high-temperature tolerant species from irrigation water in Virginia. Mycotaxon 126:167–176

    Article  Google Scholar 

  • Yang ZL (1991) Clarkeinda trachodes, an agaric new to China. Acta Bot Yunnanica 13:279–282

    Google Scholar 

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

    Google Scholar 

  • Yang ZL, Doi Y (1999) A contribution to the knowledge of Amanita (Amanitaceae, Agaricales) in Japan. Bull Natl Sci Mus Tokyo 25:108–130

    Google Scholar 

  • Yang ZL, Li TH, Wu XL (2001) Revision of Amanita collections made from Hainan, Southern China. Fungal Divers 6:149–165

    Google Scholar 

  • Yang ZL, Weiß M, Oberwinkler F (2004) New species of Amanita from the eastern Himalaya and adjacent regions. Mycologia 96:636–646

    Article  PubMed  Google Scholar 

  • Yang ZL, Li YC, Tang LP, Shi GQ, Zeng G (2012) Trogia venenata (Agaricales), a novel poisonous species which has caused hundreds of deaths in southwestern China. Mycol Prog 11:937–945

    Article  Google Scholar 

  • Yang ZL, Feng B, Hao YJ (2013) Pseudoarmillariella bacillaris, a new species with bacilliform basidiospores in Asia. Mycosystema 32:132–132

    Google Scholar 

  • Yang ZL, Qin J, Xia CF, Hu Q, Li QQ (2015b) Ophiocordyceps highlandensis, a new entomopathogenic fungus from Yunnan, China. Phytotaxa 204:287–295

    Article  Google Scholar 

  • Zalar P, Hennebert GL, Gunde-Cimerman N, Cimerman A (1997) Mucor troglophilus, a new species from cave crickets. Mycotaxon 65:507–516

    Google Scholar 

  • Zang M, Li TH, Petersen RH (2001) Five new species of Boletaceae from China. Mycotaxon 80:481–487

    Google Scholar 

  • Zeng NK, Tang LP, Li YC, Tolgor B, Zhu XT, Zhao Q, Yang ZL (2013) The genus Phylloporus (Boletaceae, Boletales) from China: morphological and multi-locus DNA sequence analyses. Fungal Divers 58:73–101

    Article  Google Scholar 

  • Zeng NK, Wu G, Li YC, Liang ZQ, Yang ZL (2014) Crocinoboletus, a new genus of Boletaceae (Boletales) with unusual boletocrocin polyene pigments. Phytotaxa 175:133–140

    Article  Google Scholar 

  • Zhang LF, Yang JB, Yang ZL (2004) Molecular phylogeny of eastern Asian species of Amanita (Agaricales, Basidiomycota): taxonomic and biogeographic 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 98:1077–1088

    Article  Google Scholar 

  • Zhang P, Chen ZH, Xiao B, Tolgor B, Bao HY, Yang ZL (2010) Lethal amanitas of East Asia characterized by morphological and molecular data. Fungal Divery 42:119–133

    Article  Google Scholar 

  • Zhang P, Yang ZL, Ge ZW (2005) Two new species of Ramaria from southwestern China. Mycotaxcon 94:235–240

    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 (2009) 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, Crous PW, Schoch CL, Hyde KD (2012) Pleosporales. Fungal Divers 53:1–221

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zhang Y, Zhang X, Fournier J, Chen J, Hyde KD (2014) Lindgomyces griseosporus, a new aquatic ascomycete from Europe including new records. Mycoscience 55:43–48

    Article  CAS  Google Scholar 

  • Zhao GC, Zhao RL (2012) The higher microfungi from forests of Yunnan Province. Yunnan Science and Technology Press, Kunming

    Google Scholar 

  • Zhao JD, Zhang XQ (2000) Flora Fungorum Sinicorum. Vol. 8. Ganodermataceae. Science Press, Beijing

    Google Scholar 

  • Zhao K, Wu G, Yang ZL (2014) A new genus, Rubroboletus, to accommodate Boletus sinicus and its allies. Phytotaxa 188:61–77

    Article  Google Scholar 

  • Zhao RL, Yang YM, Zhao GC (2004) Pseudolachnella vermospora sp. nov. from Yushania vigens in China. Fungal Divers 15:255–260

    Google Scholar 

  • Zhao RL, Karunarathna SC, Raspé O, Parra LA, Guinberteau J, Moinard M, Kesel AD, Barroso G, Courtecuisse R, Hyde KD, Guelly AK, Desjardin DE, Callac P (2011) Major clades in tropical Agaricus. Fungal Divers 51:279–296

    Article  Google Scholar 

  • Zhao RL, Zhou JL, Chen J et al. (2016) Towards standardizing taxonomic ranks using divergence times – a case study for reconstruction of the Agaricus taxonomic system. Fungal Divers. doi:10.1007/s13225-016-0357-x

  • Zhou LW (2015a) Cylindrosporus flavidus gen. et comb. nov. (Hymenochaetales, Basidiomycota) segregated from Onnia. Phytotaxa 219:276–282

    Article  Google Scholar 

  • Zhou LW (2015b) Four new species of Phylloporia (Hymenochaetales, Basidiomycota) from tropical China with a key to Phylloporia species worldwide. Mycologia 107:1184–1192

    Article  PubMed  Google Scholar 

  • Zhou LW, Dai YC (2012) Phylogeny and taxonomy of Phylloporia (Hymenochaetales): new species and a worldwide key to the genus. Mycologia 104:211–222

    Article  PubMed  Google Scholar 

  • Zhou LW, Vlasák J, Decock C, Assefa A, Stenlid J, Abate D, Wu SH, Dai YC (2016a) Global diversity and taxonomy of the Inonotus linteus complex (Hymenochaetales, Basidiomycota): Sanghuangporus gen. nov., Tropicoporus excentrodendri and T. guanacastensis gen. et spp. nov., and 17 new combinations. Fungal Divers. doi:10.1007/s13225-015-0335-8

    Google Scholar 

  • Zhou LW, Vlasák J, Qin WM, Dai YC (2016b) Global diversity and phylogeny of the Phellinus igniarius complex (Hymenochaetales, Basidiomycota) with the description of five new species. Mycologia 108:192–204

    Article  PubMed  Google Scholar 

  • Zhou W, Yuan H, Wang J, Yao J (2008) Production, purification and characterization of chitosanase produced by Gongronella sp. JG. Lett Appl Microbiol 46:49–54

    CAS  PubMed  Google Scholar 

  • Zogg H (1962) Die Hysteriaceaes. str. und Lophiaceae, unter besonderer Berücksichtigung der mitteleuropäischen Formen. Beitr Kryptogamenflora Schweiz Band 11:1–190

    Google Scholar 

Download references

Acknowledgments

G.J. Li, H.A. Wen, X.Z. Liu, M.Q. He, and R.L. Zhao thank the National Natural Science Foundation of China (No. 30770013, No. 31500013, No. 31000013, No. 31360014, No. 31470152), the Special Program of Basic Science of the Ministry of Science and Technology (No. 2012FY111600), the Technology of and International Cooperation Program of the Ministry of Science and Technology (No. 2009DFA31160) of the People’s Republic of China, and the opening funding of State key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences for funding. They are also grateful to S.P. Jiang, A.G. Xu (Xizang Institute of Plateau Biology), Wangmu (Agriculture and Animal Husbandry College of Xizang), R. Wang, S.P. Wan (Kunming Institute of Botany, Chinese Academy of Sciences), T.Z. Wei, W.L. Lu, R.H. Yang, X.Y. Liu, X.Y. Li, L. Jiang, B.B. Li, Y. Li, Y. Yu, M.J. Zhao, H. Li, S.H. Jiang, Z.X. Zhu, and J. Bing for assistance in specimen collecting; to Y.J. Yao, H.M. Lü, Q.R. Yan, and L. Yang for loans of herbarium specimens; to X.F. Zhu for inking in line drawings; to X.L. Wang for providing advice and suggestions in the phylogenetic analysis; to C.L. Li, X.L. Zhang, and J.N. Liang (Institute of Microbiology, Chinese Academy of Sciences) for providing help with SEM photography. S. Mongkolsamrit, D. Thanakitpipattana and J.J. Luangsa-ard thank National Center for Genetic Engineering and Biotechnology (BIOTEC) for project “Surveys and Collection Invertebrate-Pathogenic Fungi and Xylariaceae on Forests Conservation of Thailand” grant number P-14-51240. They would also like to thank M. Tanticharoen, K. Kirtikara, L. Eurwilaichitr and R. Tantalakha for their support of the program “Biodiversity studies of entomopathogenic fungi in Thailand”. They are grateful to the Department of National Parks, Wildlife and Plant Conservation for their cooperation and support to our project research. A.LCM de A. Santiago thanks the Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco (FACPE - APQ 0842-2.12/14), the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq - 458391/2014-0) and the Programa de Pesquisa em Biodiversidade do semiárido (MCT/CNPQ/PPBio - 457498/2012-9). T. Boonpratuang, S. Parnmen, and T. Thummarukcharoen thank the National Science and Technology Development Agency (NSTDA) Cluster and Management Program Office (CPMO) for the flagship project “Raising the quality and standards of microorganism data for use in biotechnology” grant number P-12-01829 and the Thailand Research Fund (TRG5780217) and Department of Medical Sciences, Ministry of Public Health. They also express appreciation to T. Flegel for encouragement of working on mushroom taxonomy and especially on poisonous mushrooms, L. Eurwilaichitr for funding support for molecular identification through BBH, and always support on mushroom taxonomy and M. Tanticharoen for forever support in biodiversity and taxonomy study in Thai fungi. They also thank the SRRT Team, Bureau of Epidemiology, Department of Disease Control Ministry of Public Health for collecting a specimen of poisonous mushroom in Thailand. Moreover, and toxicology center staffs (NIH: Department of Medical Sciences, Ministry of Public Health) for their suggestion and knowledge of peptide toxins identification. D. Chakraborty, K. Das, A. Baghela, S.K. Singh, and B.T.M. Dentinger thank the Director, Botanical Survey of India, Kolkata and Agharkar Research Institute, Pune for providing facilities during this study. Two of them (D. Chakraborty & K. Das) are thankful to the entire forest department of Sikkim for allowing them to undertake the macrofungal exploration in the restricted subalpine areas of North Sikkim. K. Das are indebted to Z.L. Yang (Chinese Academy of Sciences, China) for his indispensible suggestions and literature help in this regard. Field assistance rendered by S. Pradhan (BSI, Gangtok) is also duly acknowledged. A.V. Marano, A.L. Jesus, J.I. de Souza, G.H. Jerônimo, T.Y. James, M.C. Boro, S.C.O. Rocha, E.M. Leaño, M.J. Iribarren, and C.L.A. Pires-Zottarelli thank “Instituto Florestal” for the permission for sampling at the PEIC, M.O. Neves Junior for his valuable help during sampling, and to C.C. Aparecido, curator of the culture collection MMBF, for accepting our voucher cultures. They also thank São Paulo Research Foundation (FAPESP) for the fellowships given to A.L. Jesus (Process N° 2013/01409-0) and for the financial support given to C.L.A. Pires-Zottarelli (Process N° 2012/50222-7), CAPES (“Coordenação de Aperfeiçoamento de Pessoal de Nível Superior”) for the fellowship and support given to A.V. Marano (“Ciência Sem Fronteiras” Program, “Atração de Jovens Talentos” DRI-CAPES Process N° 006/2012) and CNPq (“Conselho Nacional de Desenvolvimento Científico e Tecnológico”) for the grant given to C.L.A. Pires-Zottarelli (Process N° 304411/2012-4). L.W. Zhou, Y.C. Dai and J. Vlasák thank O. Euatrakool and A. Auetragul for their help in field trip. They also thank National Natural Science Foundation of China (Project No. 31200015). T. Niskanen, K. Liimatainen, M. Beug, and J. Ammirati are grateful to D.E. Stuntz Memorial Foundation. M.A. Abdel-Wahab, A.H. Bahkali, E.B.G. Jones and F.A. Abdel-Aziz thank the National Plan for Science, Technology and Innovation (MAARIFAH), King Abdulaziz City for Science and Technology, Kingdom of Saudi Arabia, Award Number (12-BIO2840-02). E. Kuhnert, E.B. Sir, and M. Stadler are grateful to A.I. Hladki for her contribution to the collection of Argentinian specimens. They thank C. Lambert and S. Heitkämper for obtaining the cultures and performing the molecular work. M. Rohde is thanked for SEM recordings. Funding from the DAAD and the Argentina Ministerio de Ciencia, Tecnología e Innovación Productiva for an academic exchange program involving E. Kuhnert, E.B. Sir and M. Stadler is gratefully acknowledged. T.C. Wen, K.K. Hapuarachchi and K.D. Hyde thank the National Natural Science Foundation of China (No. 31460012) and the Science Foundation of Guizhou University (No. 201309). E. De Crop is supported by the “Special Research Fund Ghent University” (BOF). The survey in Thailand was part of the Northern Thailand mushroom diversity workshop prior to the 10th International Mycological Congress and was financially supported by the Research Foundation Flanders (FWO, grant K1A7614N). F. Hampe is thanked by M. Verbeken for conducting laboratory work. K. Tanaka would like to thank the Japan Society for the Promotion of Science (JSPS, 25440199 and 26291084) and Hirosaki University Grant for Exploratory Research by Young Scientists and Newly appointed Scientists for financial support. B.K. Cui, J. Song and J.J. Chen are grateful to H.S. Yuan (IFP, China) for loan of specimens. The research was supported by the National Natural Science Foundation of China (Project No. 31422001). B. Thongbai was financial supported by the Royal Golden Jubilee-Industry Ph.D (Ph.D/0138/2553 in 4.S.MF/53/A.3). We thank the International Research Group Program (IRG-14-27), Deanship of Scientific Research, King Saud University, Saudi Arabia for partially supporting this research. K.D. Hyde thanks the Chinese Academy of Sciences, [project number 2013T2S003], for the award of Visiting Professorship for Senior International Scientists at Kunming Institute of Botany. MFLU [grant number 56101020032] is thanked for supporting studies on Dothideomycetes. We are grateful to the Mushroom Research Foundation, Chiang Rai, Thailand. C.G. Lin is grateful to J.Z. Sun (Mae Fah Luang University, Thailand) for comments on the manuscript and S.F. Ran (Guizhou University, Guizhou, China) for assistance in molecular work, and to the support by the National Natural Science Foundation of China (No. NSFC 31560489). N.N. Wijayawardene thanks Guizhou University for helping to carryout DNA sequencing. T.T.T. Nguyen, S.J. Jeon, H.S. Lee, P.M. Kirk, K. Voigt and H.B. Lee were 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 of the Ministry of Environment (MOE), Republic of Korea. M. 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. C. Phukhamsakda would like to thank the Royal Golden Jubilee PhD Program under Thailand Research Fund, for the award of a scholarship no. PHD/0020/2557 to study towards a PhD. M. Gorczak was supported by Polish Ministry of Science and Higher Education under grant no. DI2014012344. J. Pawłowska was partially supported by the National Science Center of Poland under grant no. 2015/17/D/NZ8/00778. M. Abdel-Wahab was funded by the National Plan for Science, Technology and Innovation (MAARIFAH), King Abdulaziz City for Science and Technology, Kingdom of Saudi Arabia, Award Number (12-BIO2840-02). J. Zhao, G. Consiglio, P. Alvarado, S.D. Yang, L. Setti, Y. Hu, A. Vizzini, and L.P. Tang wish to express their sincere gratitude to Swiss mycologist E Musumeci (Basel, Switzerland) for providing valuable information (including photographs) on Musumecia vermicularis. They are grateful to J.F. Liang (Research Institute of Tropical Forestry, Chinese Academy of Forestry) for helping to scan basidiospores. This work was financially supported by the National Natural Science Foundation of China (No. 31560004), Yunnan applied basic research projects-joint special project (No. 2014FB016), the Science Research Foundation of department of education, Yunnan Province (No. 2015Y147), and the Open Research Foundation of Yunnan Key Laboratory of Pharmacology for Natural Products (No. 2015G003). G. Alves-Silva, A. Góes-Neto and E.R. Drechsler-Santos thank the Parque Natural Municipal São Francisco de Assis for permission to sample collections and F. Bittencourt for specimen collected and pictures in situ; herbaria mentioned (FURB and FLOR); Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) for providing a master’s scholarship to G. Alves-Silva; Fiocruz for performing the molecular sequencing; PPGFAP/UFSC and BrBOL for partial financing of the research. M.A. Reck thanks CAPES (PNPD Institucional 2011—23038.007790/2011-93) for scholarship and funding. P. Chomnunti would like to thank the National Research Council of Thailand (NRCT), for the project “Biodiversity, phylogeny and biological activity of Dothideomycetes” grant number 58201020010 and Thailand Research Fund (TRF) grant number TRG5780008 for partial funding. R. Phookamsak sincerely appreciates The Royal Golden Jubilee Ph. D. Program (PHD/0090/2551) under the Thailand Research Fund for financial support. S.C. Karunarathna 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)2013BAB07B06 integration and comprehensive demonstration of key technologies on Green Phosphate-mountaion Construction; the CGIAR Research Program 6: Forest, Trees and Agroforestry; and the National Research Council of Thailand (NRCT), projects - Taxonomy, phylogeny and cultivation of Lentinus species in northern Thailand (NRCT/55201020007) for partial funding. K.V. Solomon, J.K. Henske, C.H. Haitjema, S.P. Gilmore, M.K. Theodorou, and M.A. O’Malley thanks the Office of Science (BER), U.S. Department of Energy (DE-SC0010352) and the Institute for Collaborative Biotechnologies through grant W911NF-09-0001, and the Mellichamp Academic Initiative in Sustainability at UC Santa Barbara. A portion of their research was performed under the JGI-EMSL Collaborative Science Initiative and used resources at the DOE Joint Genome Institute and the Environmental Molecular Sciences Laboratory, which are DOE Office of Science User Facilities. Both facilities are sponsored by the Office of Biological and Environmental Research and operated under Contract Nos. DE-AC02-05CH11231 (JGI) and DE-AC05-76RL01830 (EMSL).

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Li, G.J., Hyde, K.D., Zhao, R.L. et al. Fungal diversity notes 253–366: taxonomic and phylogenetic contributions to fungal taxa. Fungal Diversity 78, 1–237 (2016). https://doi.org/10.1007/s13225-016-0366-9

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