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Monday 19 June 2017

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

Published Date
Volume 83, Issue 1pp 1–261

DOI: 10.1007/s13225-017-0378-0
Cite this article as:
Tibpromma, S., Hyde, K.D., Jeewon, R. et al. Fungal Diversity (2017) 83: 1. doi:10.1007/s13225-017-0378-0
Author
  • Saowaluck Tibpromma
  • Kevin D. Hyde
  • Rajesh Jeewon
  • Sajeewa S. N. Maharachchikumbura
  • Jian-Kui Liu
  • D. Jayarama Bhat
  • E. B. Gareth Jones
  • Eric H. C. McKenzie
  • Erio Camporesi
  • Timur S. Bulgakov
  • Mingkwan Doilom
  • André Luiz Cabral Monteiro de Azevedo Santiago
  • Kanad Das
  • Patinjareveettil Manimohan
  • Tatiana B. Gibertoni
  • Young Woon Lim
  • Anusha Hasini Ekanayaka
  • Benjarong Thongbai
  • Hyang Burm Lee
  • Jun-Bo Yang
  • Paul M. Kirk
  • Phongeun Sysouphanthong
  • Sanjay K. Singh
  • Saranyaphat Boonmee
  • Wei Dong
  • K. N. Anil Raj
  • K. P. Deepna Latha
  • Rungtiwa Phookamsak
  • Chayanard Phukhamsakda
  • Sirinapa Konta
  • Subashini C. Jayasiri
  • Chada Norphanphoun
  • Danushka S. Tennakoon
  • Junfu Li
  • Monika C. Dayarathne
  • Rekhani H. Perera
  • Yuanpin Xiao
  • Dhanushka N. Wanasinghe
  • Indunil C. Senanayake
  • Ishani D. Goonasekara
  • N. I. de Silva
  • Ausana Mapook
  • Ruvishika S. Jayawardena
  • Asha J. Dissanayake
  • Ishara S. Manawasinghe
  • K. W. Thilini Chethana
  • Zong-Long Luo
  • Kalani Kanchana Hapuarachchi
  • Abhishek Baghela
  • Adriene Mayra Soares
  • Alfredo Vizzini
  • Angelina Meiras-Ottoni
  • Armin Mešić
  • Arun Kumar Dutta
  • Carlos Alberto Fragoso de Souza
  • Christian Richter
  • Chuan-Gen Lin
  • Debasis Chakrabarty
  • Dinushani A. Daranagama
  • Diogo Xavier Lima
  • Dyutiparna Chakraborty
  • Enrico Ercole
  • Fang Wu
  • Giampaolo Simonini
  • Gianrico Vasquez
  • Gladstone Alves da Silva
  • Helio Longoni PlautzJr.
  • Hiran A. Ariyawansa
  • Hyun Lee
  • Ivana Kušan
  • Jie Song
  • Jingzu Sun
  • Joydeep Karmakar
  • Kaifeng Hu
  • Kamal C. Semwal
  • Kasun M. Thambugala
  • Kerstin Voigt
  • Krishnendu Acharya
  • Kunhiraman C. Rajeshkumar
  • Leif Ryvarden
  • Margita Jadan
  • Md. Iqbal Hosen
  • Michal Mikšík
  • Milan C. Samarakoon
  • Nalin N. Wijayawardene
  • Nam Kyu Kim
  • Neven Matočec
  • Paras Nath Singh
  • Qing Tian
  • R. P. Bhatt
  • Rafael José Vilela de Oliveira
  • Rodham E. Tulloss
  • S. Aamir
  • Saithong Kaewchai
  • Sayali D. Marathe
  • Sehroon Khan
  • Sinang Hongsanan
  • Sinchan Adhikari
  • Tahir Mehmood
  • Tapas Kumar Bandyopadhyay
  • Tatyana Yu. Svetasheva
  • Thi Thuong Thuong Nguyen
  • Vladimír Antonín
  • Wen-Jing Li
  • Yong Wang
  • Yuvraj Indoliya
  • Zdenko Tkalčec
  • Abdallah M. Elgorban
  • Ali H. Bahkali
  • Alvin M. C. Tang
  • Hong-Yan Su
  • Huang Zhang
  • Itthayakorn Promputtha
  • Jennifer Luangsa-ard
  • Jianchu Xu
  • Jiye Yan
  • Kang Ji-Chuan
  • Marc Stadler
  • Peter E. Mortimer
  • Putarak Chomnunti
  • Qi Zhao
  • Alan J. L. Phillips
  • Sureeporn Nontachaiyapoom
  • Ting-Chi Wen
  • Samantha C. Karunarathna
Abstract
This is a continuity of a series of taxonomic and phylogenetic papers on the fungi where materials were collected from many countries, examined and described. In addition to extensive morphological descriptions and appropriate asexual and sexual connections, DNA sequence data are also analysed from concatenated datasets to infer phylogenetic relationships and substantiate systematic positions of taxa within appropriate ranks. Wherever new species or combinations are proposed, we apply an integrative approach using morphological and molecular data as well as ecological features wherever applicable. Notes on 112 fungal taxa are compiled in this paper including Biatriosporaceae and RoussoellaceaeDidysimulans gen. nov., 81 new species, 18 new host records and new country records, five reference specimens, two new combinations, and three sexual and asexual morph reports. The new species are Amanita corneliiAemodotrygonAngustimassarina alniAarezzoensisAitalicaAloniceraeApremilcurensisAscochyta italicaArosaeAustroboletus appendiculatusBarriopsis thailandicaBerkleasmium arienseCalophoma petasitisCamarosporium laburnicolaCmoricolaCgriseaCosseaCparaincrustataColletotrichum sambucicolaCoprinopsis cerkeziiCytospora gelidaDacrymyces chiangraiensisDidysimulans italicaDmezzanensisEntodesmium italicaEntoloma magnumEvlachovaea indicaExophiala italicaFavolus gracilisporusFemsjonia monosporaFomitopsis flabellataFroseoalbaGongronella brasiliensisHelvella crispoidesHermatomyces chiangmaiensisHchromolaenaeHysterium centramurumInflatispora caryotaeInocybe brunneosquamulosaIluteobrunneaIrubrobrunneaKeissleriella cirsiiLepiota cylindrocystidiaLflavocarpaLmaerimensisLophiotrema guttulataMarasmius luculentusMorenoina calamicolaMoelleriella thanathonensisMucor stercorariusMyrmecridium fluviaeMyrothecium septentrionaleNeosetophoma garethjonesiiNigrograna cangshanensisNodulosphaeria guttulatumNmultiseptataNsambuciPanus subfasciatusParaleptosphaeria padiParaphaeosphaeria viciaeParathyridaria robiniaePenicillium punicaePhaeosphaeria calamicolaPhaeosphaeriopsis yuccaePleurophoma italicaPolyporus brevibasidiosusPkoreanusPorientivariusPparvovariusPsubdictyopusPulleungusPseudoasteromassaria spadiceaRosellinia mearnsiiRubroboletus demonensisRussula yanheensisSigarispora muriformisSillia italicaStagonosporopsis ailanthicolaStrobilomyces longistipitatusSubplenodomus galicola and Wolfiporia pseudococos. The new combinations are Melanomma populina and Rubroboletus eastwoodiae. The reference specimens are Cookeina tricholomaGnomoniopsis sanguisorbaeHelvella costiferaPolythrincium trifolii and Russula virescens. The new host records and country records are Ascochyta medicaginicolaBoletellus emodensisCyptotrama asprataCytospora ceratospermaFavolaschia auriscalpiumFmanipularisHysterobrevium moriLentinus sajor-cajuLsquarrosulusLvelutinusLeucocoprinus cretaceusLophiotrema vagabundumNothophoma quercinaPlatystomum rosaePseudodidymosphaeria phleiTremella fuciformisTruncatella spartii and Vaginatispora appendiculata and three sexual and asexual morphs are Aposphaeria corallinoluteaDothiora buxi and Hypocrella calendulina.

References
  1. Aalto M (1974) Amanita magnivolvata sp. nova (Agaricales). Karstenia 14:93–96Google Scholar
  2. Abbott SP, Currah RS (1997) The Hevellaceae: systematic revision and occurrence in northern and northwestern North America. Mycotaxon 62:1–125Google Scholar
  3. Abdollahzadeh J, Goltapeh EM, Javadi A, Shams-Bakhsh M, Zare R, Phillips AJL (2009) Barriopsis iraniana and Phaeobotryon cupressi, two new species of the Botryosphaeriaceae from trees in Iran. Persoonia 23:1–8PubMedPubMedCentralCrossRefGoogle Scholar
  4. Adamčík S, Cai L, Chakraborty D, Chen XH, Cotter H, Van T, Dai DQ, Dai YC, Sas K, Deng C, Ghobad-Nejhad M, Hyde KD, Langer E, Latha KPD, Liu F, Liu SL, Liu T, Wei LV, Shu-Xia LV, Machado AR, Pinho DB, Pereira OL, Prasher IB, Rosado AWC, Qin J, Qin WM, Verma RK, Wang Q, Yang ZL, Yu XD, Zhou LW, Buyck B (2015) Fungal biodiversity profiles 1–10. Cryptogam Mycol 36:121–166CrossRefGoogle Scholar
  5. Adams GC, Wingfield MJ, Common R, Roux J (2005) Phylogenetic relationships and morphology of Cytospora species and related teleomorphs (Ascomycota, DiaporthalesValsaceae) from Eucalyptus. Stud Mycol 52:1–144Google Scholar
  6. Adams GC, Roux J, Wingfield MJ (2006) Cytospora species (Ascomycota, DiaporthalesValsaceae): introduced and native pathogens of trees in South Africa. Australas Plant Pathol 35:521–548CrossRefGoogle Scholar
  7. Addy HD, Piercey MM, Currah RS (2005) Microfungal endophytes in roots. Can J Bot 83:1–13CrossRefGoogle Scholar
  8. Ahmad S (1969) Fungi of West Pakistan, supplement 1. Society at the Biological Laboratories, Government College, LahoreGoogle Scholar
  9. Ahmad S, Iqbal SH, Khalid AN (1997) Fungi of Pakistan. Sultan Ahmad Mycological Society of Pakistan, Department of Botany, University of the Punjab, LahoreGoogle Scholar
  10. Aime L, Ryvarden L, Henkel TW (2007) Studies in Neotropicalpolypores 22. Additional new and rare species from Guyana. Synop Fungorum 23:15–31Google Scholar
  11. Alvarado P, Manjon JL, Matheny PB, Esteve-Raventos F (2010) Tubariomyces, a new genus of Inocybaceae from the Mediterranean region. Mycologia 102:1389–1397PubMedCrossRefGoogle Scholar
  12. Andersson M (2013) A rare bolete, Boletus legaliae, in the Royal Garden of Drottningholm, Stockholm. Sven Mykol Tidskr 34(3):9–13Google Scholar
  13. Antonín V, Buyck B (2006) Marasmius (Basidiomycota, Marasmiaceae) in Madagascar and the Mascarenes. Fungal Divers 23:17–50Google Scholar
  14. Antonín V (2007) Monograph of MarasmiusGloiocephalaPalaeocephala and Setulipes in tropical Africa. Fungus Flora Trop Afr 1:1–177Google Scholar
  15. Antonín V, Vizzini A, Ercole E, Leonardi M (2015) Strobilomyces pteroreticulosporus (Boletales), a new species of the S. strobilaceus complex from the Republic of Korea and remarks on the variability of S. confuses. Phytotaxa 219(1):78–86CrossRefGoogle Scholar
  16. Ariyawansa HA, Tanaka K, Thambugala KM, Phookamsak R, Tian Q, Camporesi E, Hongsanan S, Monkai J, Wanasinghe DN, Mapook A, Chukeatirote E (2014a) A molecular phylogenetic reappraisal of the Didymosphaeriaceae (=Montagnulaceae). Fungal Divers 68:69–104CrossRefGoogle Scholar
  17. Ariyawansa HA, Hawksworth DL, Hyde KD, Jones EG, Maharachchikumbura SS, Manamgoda DS, Thambugala KM, Udayanga D, Camporesi E, Daranagama A, Jayawardena R (2014b) Epitypification and neotypification: guidelines with appropriate and inappropriate examples. Fungal Divers 69(1):57–91CrossRefGoogle Scholar
  18. Ariyawansa HA, Phukhamsakda C, Thambugala KM, Bulgakov TS, Wanasinghe DN, Perera RH, Mapook A, Camporesi E, Kang JC, Jones EG, Bahkali AH (2015a) Revision and phylogeny of Leptosphaeriaceae. Fungal Divers 74:19–51CrossRefGoogle Scholar
  19. Ariyawansa HA, Thambugala KM, Manamgoda DS, Jayawardena R, Camporesi E, Boonmee S, Wanasinghe DN, Phookamsak R, Hongsanan S, Singtripop C, Chukeatirote E (2015b) Towards a natural classification and backbone tree for Pleosporaceae. Fungal Divers 71(1):85–139CrossRefGoogle Scholar
  20. Ariyawansa HA, Hyde KD, Jayasiri SC, Buyck B, Chethana KWT, Dai DQ, Dai YC, Daranagama DA, Jayawardena RS, Lücking R, Ghobad-Nejhad M, Niskanen T, Thambugala KM, Voigt K, Zhao RL, Li GJ, Doilom M, Boonmee S, Yang ZL, Cai Q, Cui YY, Bahkali AH, Chen J, Cui BK, Chen JJ, Dayarathne MC, Dissanayake AJ, Ekanayaka AH, Hashimoto A, Hongsanan S, Jones EBG, Larsson E, Li WJ, Li QR, Liu JK, Luo ZL, Maharachchikumbura SSN, Mapook A, McKenzie EHC, Norphanphoun C, Konta S, Pang KL, Perera RH, Phookamsak R, Phukhamsakda C, Pinruan U, Randrianjohany E, Singtripop C, Tanaka K, Tian CM, Tibpromma S, Abdel-Wahab MA, Wanasinghe DN, Wijayawardene NN, Zhang JF, Zhang H, Abdel- Aziz FA, Wedin M, Westberg M, Ammirati JF, Bulgakov TS, Lima DX, Callaghan TM, Callac P, Chang CH, Coca LF, Dal-Forno M, Dollhofer V, Fliegerová K, Greiner K, Griffith GW, Ho HM, Hofstetter V, Jeewon R, Kang JC, Wen TC, Kirk PM, Kytövuori I, Lawrey JD, Xing J, Li H, Liu ZY, Liu XZ, Liimatainen K, Thorsten Lumbsch H, Matsumura M, Moncada B, Nuankaew S, Parnmen S, Santiago ALCMA, Sommai S, Song Y, de Souza CAF, de Souza- Motta CM, Su HY, Suetrong S, Wang Y, FongWS YH, Zhou LW, Réblová M, Fournier J, Camporesi E, Luangsa-ard JJ, Tasanathai K, Khonsanit A, Thanakitpipattana D, Somrithipol S, Diederich P, Millanes AM, Common RS, Stadler M, Yan JY, Li XH, Lee HW, Nguyen TTT, Lee HB, Battistin E, Marsico O, Vizzini A, Vila J, Ercole E, Eberhardt U, Simonini G, Wen HA, Chen XH, Miettinen O, Spirin V, Hernawati (2015c) Fungal diversity notes 111–252 taxonomic and phylogenetic contributions to fungal taxa. Fungal Divers 75:27–274CrossRefGoogle Scholar
  21. Arora D, Ferrarese G, Simonini G (1999) Boletus pulcherrimus Boletus rubrosanguineus: lo stesso taxon? Micol Veget Medit 14(2):116–141Google Scholar
  22. Arun Kumar TK, Manimohan P (2009) The genus Lepiota (Agaricales, Basidiomycota) in Kerala State, India. Mycotaxon 107:105–138CrossRefGoogle Scholar
  23. Arzanlou M, Groenewald JZ, Gams W, Braun U, Shin HD, Crous PW (2007) Phylogenetic and morphotaxonomic revision of Ramichloridium and allied genera. Stud Mycol 58:57–93PubMedPubMedCentralCrossRefGoogle Scholar
  24. Aveskamp MM, de Gruyter J, Crous PW (2008) Biology and recent developments in the systematics of Phoma, a complex genus of major quarantine significance. Fungal Divers 31:1–18Google Scholar
  25. Aveskamp MM, de Gruyter J, Woudenberg JHC, Verkley GJM, Crou PW (2010) Highlights of the Didymellaceae: a polyphasic approach to characterise Phoma and related pleosporalean genera. Stud Mycol 65:1–60PubMedPubMedCentralCrossRefGoogle Scholar
  26. Bahl J, Jeewon R, Hyde KD (2005) Phylogeny of Rosellinia capetribulensis sp. nov. and its allies (Xylariaceae). Mycologia 97:1102–1110PubMedCrossRefGoogle Scholar
  27. Baroni TJ, Hofstetter V, Largent DL, Vilgalys R (2011) Entocybe is proposed as a new genus in the Entolomataceae (Agaricomycetes, Basidiomycota) based on morphological and molecular evidence. N Am Fungi 6:1–19Google Scholar
  28. Barr ME (1978) The Diaporthales in North America with emphasis on Gnomonia and its segregates. Mycol Mem 7:1–232Google Scholar
  29. Barr ME (1979) A classification of Loculoascomycetes. Mycologia 71:935–957CrossRefGoogle Scholar
  30. Barr ME (1987) Prodomus to class Loculoascomycetes. Published by the Author, AmherstGoogle Scholar
  31. Barr ME (1990) Melanommatales (Loculoascomycetes). N Am Flora Ser II 13:1–129Google Scholar
  32. Barr ME (1992) Notes on the Lophiostomataceae (Pleosporales). Mycotaxon 45:191–221Google Scholar
  33. Bas C (1969) Morphology and subdivision of Amanita and a monograph of its section Lepidella. Persoonia 5:285–579Google Scholar
  34. Bas C (1974) A rare and widespread Amanita associated with Alnus. Bulletin Mensuel de la Société Linnéenne de Lyon 43:17–23CrossRefGoogle Scholar
  35. Bas C (1984) On the correct name of ‘Amanita inaurata Secr.’. Persoonia Mol Phylogeny Evol Fungi 12:192–193Google Scholar
  36. Bas C, Kuyper TW, Noordeloos ME, Vellinga EC (1995) Flora Agaricina Neerlandica—3, Tricholomataceae. A. A. Balkema, Rotterdam
  37. Bates ST, Reddy GSN, Garcia-Pichel F (2006) Exophiala crusticola anam. nov. (affinity Herpotrichiellaceae), a novel black yeast from biological soil crusts in the Western United States. Int J Syst Evol Microbiol 56:2697–2702PubMedCrossRefGoogle Scholar
  38. Bau T, Li Y, Irina AG, Eugenia MB, Wasiliy AS (2008) Common wild edible mushroom resource of Russia. Edible Fungi China 27:9–13Google Scholar
  39. Benny GL (2008) Methods used by Dr. R. K. Benjamin, and other mycologists, to isolate Zygomycetes. Aliso 26:37–61CrossRefGoogle Scholar
  40. Benny GL, Smith ME, Kirk PM, Tretter ED, White MM (2016) Challenges and Future Perspectives in the Systematics of KickxellomycotinaMortierellomycotinaMucoromycotina, and Zoopagomycotina. In: Li D-W (ed) Biology of microfungi, fungal biology. Springer, BaselGoogle Scholar
  41. Berkeley MJ (1847) Decades of fungi XII–XIV. Lond J Bot 6:312–326Google Scholar
  42. Bernicchia A, Gorjón SP (2010) Corticiaceae s.l. Fungi Europaei, vol 12. Ed Candusso, Italia
  43. Bessette AE, Roody WC, Bessette AR (2000) North American Boletes. Syracuse University Press, SyracuseGoogle Scholar
  44. Bessette AE, Roody WC, Bessette AR (2010) North American Boletes: a color guide to fleshy pored mushrooms. Syracuse University Press, SyracuseGoogle Scholar
  45. Bhatt RP, Tulloss RE, Semwal KC, Bhatt VK, Moncalvo JM, Stephenson SL (2003) Amanitaceae from India. A critically annotated checklist. Mycotaxon 88:249–270Google Scholar
  46. Binder M, Hibbett DS (2006) Molecular systematics and biological diversification of Boletales. Mycologia 98:971–981PubMedCrossRefGoogle Scholar
  47. Binder M, Justo A, Riley R, Salamov A, Lopez-Giraldez F, Sjökvist E, Copeland A, Foster B, Sun H, Larsson E, Larsson KH, Townsend J, Grigoriev IV, Hibbett D (2013) Phylogenetic and phylogenomic overview of the Polyporales. Mycologia 105:1350–1373PubMedCrossRefGoogle Scholar
  48. Binion DE, Stephenson SL, Roody WC, Burdsall HH Jr., Vasilyeva LN, Miller OK Jr. (2008) Macrofungi associated with oaks of Eastern North America. West Virginia University Press, MorgantownGoogle Scholar
  49. Bisby GR, Buller AHR, Dearness J (1929) The fungi of Manitoba. Longmans, Green and Co, LondonGoogle Scholar
  50. Boehm EW, Schoch CL, Spatafora JW (2009a) On the evolution of the Hysteriaceae and Mytilinidiaceae (Pleosporomycetidae, Dothideomycetes, Ascomycota) using four nuclear genes. Mycol Res 113:461–479PubMedCrossRefGoogle Scholar
  51. Boehm EWA, Mugambi G, Miller AN, Huhndorf S, Marincowitz S, Schoch CL, Spatafora JW (2009b) A molecular phylogenetic reappraisal of the HysteriaceaeMytilinidiaceae and Gloniaceae (Pleosporomycetidae, Dothideomycetes) with keysto world species. Stud Mycol 64:49–83PubMedPubMedCentralCrossRefGoogle Scholar
  52. Bolay A (1971) Contribution a la connaissance de Gnomonia comari Karsten (syn. G. fructicola [Arnaud] Fall). Etude taxonomique, phytopathologique et recherches sur sa croissance in vitro. Ber Schweizerischen Bot Ges 81:398–482Google Scholar
  53. Borisov BA, Tarasov KL (1999) Notes on biodiversity of causal agents of invertebrate mycoses in Adjaria (south-western Georgia). I. Evlachovaea kintrischica gen. et sp. nov. (Hyphomycetes) from Kintrishi Reservation. Mikologiya i Fitopatologiya 33(4):248–256Google Scholar
  54. Breitenbach J, Kränzlin F (1991) Fungi of Switzerland, vol. 3, Boletes and Agarics 1st part. Mykologia, Lucerne, Switzerland
  55. Bresadola J (1896) Fungi Tridentini. 195 plates. 1881–1900. Contains figures of Hydnaceae. Fungi Brasilienses. Hedwigia 35:276–302Google Scholar
  56. Bukovská P, Jelínková M, Hršelová H, Sýkorová Z, Gryndler M (2010) Terminal restriction fragment length measurement errors are affected mainly by fragment length, G+C nucleotide content and secondary structure melting point. J Microbiol Methods 82:223–228PubMedCrossRefGoogle Scholar
  57. Bussaban B, Lumyong S, Lumyong P, Mckenzie EHC, Hyde KD (2001) A synopsis of the genus Berkleasmium with two new species and new records of Canalisporium caribense from Zingiberaceae in Thailand. Fungal Divers 8:73–85Google Scholar
  58. Buyck B, Hofstetter V, Eberhardt U, Verbeken A, Kauff F (2008) Walking the thin line between Russula and Lactarius: the dilemma of Russula subsect. Ochricompactae. Fungal Divers 28:15–40Google Scholar
  59. Buyck B, Hofstetter V, Verbeken A, Walleyn R (2010) (1919) Proposal to conserve Lactarius nom. cons. (Basidiomycota) with a conserved type. Taxon 59(1):295–296Google Scholar
  60. Cai L, Jeewon R, Hyde KD (2006) Phylogenetic investigations of Sordariaceae based on multiple gene sequences and morphology. Mycol Res 110:137–150PubMedCrossRefGoogle Scholar
  61. Calzada Dominguez A (2007) Guía de los Boletos de España y Portugal. Náyade Editorial, Medina del Campo, Valladolid
  62. Câmara MPS, Palm ME, van Berkum P, O’Neill NR (2002) Molecular phylogeny of Leptosphaeria and Phaeosphaeria. Mycologia 94:630–640PubMedCrossRefGoogle Scholar
  63. Câmara MP, Ramaley AW, Castlebury LA, Palm ME (2003) Neophaeosphaeria and Phaeosphaeriopsis, segregates of Paraphaeosphaeria. Mycol Res 107:516–522PubMedCrossRefGoogle Scholar
  64. Cannon PF, Kirk PM (2007) Fungal families world, 7th edn. CAB International, WallingfordGoogle Scholar
  65. Cannon PF, Hawksworth DL, Sherwood-Pike MA (1985) The British Ascomycotina. An annotated checklist. Commonwealth Mycological Institute, Kew, SurreyGoogle Scholar
  66. Cannon PF, Damm U, Johnston PR, Weir BS (2012) Colletotrichum current status and future directions. Study Mycol 73:181–213CrossRefGoogle Scholar
  67. Carbone I, Kohn LM (1999) A method for designing primer sets for speciation studies in filamentous ascomycetes. Mycologia 91:553–556CrossRefGoogle Scholar
  68. Carmichael JW (1966) Cerebral mycetoma of trout due to a Phialophora-like fungus. Sabouraudia 6:120–123Google Scholar
  69. Carmichael JW (1967) Cerebral mycetoma of trout due to a Phialophora-like fungus. Sabouraudia. J Med Vet Mycol 5(2):120–123CrossRefGoogle Scholar
  70. Carson ML (2005) Yield loss potential of Phaeosphaeria leaf spot of maize caused by Phaeosphaeria maydis in the United States. Plant Dis 89:986–988CrossRefGoogle Scholar
  71. Castañeda RF, Heredia G (2000) Two new dematiaceous hyphomycetes on Cyathea from Mexico. Cryptogam Mycol 21:221–228CrossRefGoogle Scholar
  72. Castlebury LA, Rossman AY, Jaklitsch WJ, Vasilyeva LN (2002) A preliminary overview of the Diaporthales based on large subunit nuclear ribosomal DNA sequences. Mycologia 94:1017–1031PubMedCrossRefGoogle Scholar
  73. Chaverri P, Bischoff JF, Evans HC, Hodge KT (2005) Regiocrella a new entomopathogenic genus with a pycnidial anamorph and its phylogenetic placement in the Clavicipitaceae. Mycologia 97:1225–1237PubMedCrossRefGoogle Scholar
  74. Chaverri P, Liu M, Hodge KT (2008) A monograph of the entomopatho- genic genera HypocrellaMoelleriella and Samuelsia gen. nov. (AscomycotaHypocrealesClavicipitaceae) and their aschersonia-like anamorphs in the Neotropics. Stud Mycol 60:1–66PubMedPubMedCentralCrossRefGoogle Scholar
  75. Checa J, Ramaley AW, Palm-Hernández ME, Câmara MP (2002) Paraphaeosphaeria barrii, a new species on Yucca schidigera from Mexico. Mycol Res 106:375–379CrossRefGoogle Scholar
  76. Cheewangkoon R, Crous PW, Hyde KD, Groenewald JZ, To-Anan C (2008) Species of Mycosphaerella and related anamorphs on Eucalyptus leaves from Thailand. Persoonia 21:77–91PubMedPubMedCentralCrossRefGoogle Scholar
  77. Chen Q, Jiang JR, Zhang GZ, Cai L, Crous PW (2015) Resolving the Phoma enigma. Stud Mycol 82:137–217PubMedPubMedCentralCrossRefGoogle Scholar
  78. Chen Y, Ran SF, Dai DQ, Wang Y, Hyde KD, Wu YM, Jiang YL (2016) Mycosphere Essays 2. Myrothecium. Mycosphere 7:64–80Google Scholar
  79. Chen ZH, Zhang P, Zhang ZG (2013) Investigation and analysis of 102 mushroom poisoning cases in southern China from 1994 to 2012. Fungal Divers 64:123–131CrossRefGoogle Scholar
  80. Chethana KWT, Phillips AJL, Zhang W, Chen Z, Hao YY, Hyde KD, Li XH, Yan JY (2016) Mycosphere Essays 5: Is it important to name species of Botryosphaeriaceae? Mycosphere 7:870–882Google Scholar
  81. Chevallier FF (1826) Flore Générale des Environs de Paris [General Flora of the Area Around Paris]. Ferra Jeune, France, pp 1–674
  82. Cheype JL (1983) Validation de Boletus rubrosanguineus (Walty). Doc Mycol 52:53–54Google Scholar
  83. Chlebicki A, Mukhin VA, Ushakowa N (2003) Fomitopsisofficinalis on Siberian Larch in Urals. Mycologist 17:116–120CrossRefGoogle Scholar
  84. Chomnunti P, Schoch CL, Aguirre-Hudson B, KoKo TW, Hongsanan S, Jones EBG, Kodsub R, Chukeatirote E, Bahkali AH, Hyde KD (2011) Capnodiaceae. Fungal Divers 51:103–134PubMedPubMedCentralCrossRefGoogle Scholar
  85. Chomnunti P, Hongsanan S, Hudson BA, Tian Q, Peršoh D, Dhami MK, Alias AS, Xu J, Liu X, Stadler M, Hyde KD (2014) The sooty moulds. Fungal Divers 66:1–36CrossRefGoogle Scholar
  86. Chouhan JS, Panwar KS (1980) Hyphomycetes of Mount Abu-V. Indian Phytopathol 33:285–291Google Scholar
  87. Clements FE, Shear CL (1931) Genera of fungi, 2nd edn. H.W. Wilson, New YorkGoogle Scholar
  88. Co-David D, Langeveld D, Noordeloos ME (2009) Molecular phylogeny and spore evolution of Entolomataceae. Persoonia 23:147–176PubMedPubMedCentralCrossRefGoogle Scholar
  89. Consiglio G, Simonini G (2005) Trattamento statistico delle dimensioni sporali. In: Consiglio G, Antonini D, Antonini M (eds) Il Genere Cortinarius, parte III. Centro Studi Micologici AMB, pp 33–44
  90. Corda ACI (1831) Die Pilze Deutschlands. In: Sturm J (ed) Deutschlands Flora in Abbildungen nach der Natur mit Beschreibungen, vol 12(3). Sturm, Nurnberg, pp 33–64
  91. Corda ACJ (1837) Icones fungorum hucusque cognitorum, vol 1. J.G. Calve, PragueGoogle Scholar
  92. Corlett M (1981) A taxonomic survey of some species of Didymella and Didymella-like species. Can J Bot 59:2016–2042CrossRefGoogle Scholar
  93. Corner EJH (1950) A monograph of Clavaria and allied genera. Oxford University Press, OxfordGoogle Scholar
  94. Corner EJH (1970) Supplement to a monograph of Clavaria and allied genera. Beihefte zur Nova Hedwigia 33:1–299Google Scholar
  95. Corner EJH (1981) The agaric genera LentinusPanus, and Pleurotus with particular reference to Malaysian species. Nova Hedwigia 69:1–169Google Scholar
  96. Corner EJH (1996) The agaric genera MarasmiusChaetocalathusCrinipellisHeimiomycesResupinatusXerula and Xerulina in Malesia. Beih Nova Hedwigia 111:1–175Google Scholar
  97. Corner EJH, Thind KS, Anand GPS (1956) The Clavariaceae of the Mussoorie hills (India). II. Trans Br Mycol Soc 39(4):475–484CrossRefGoogle Scholar
  98. Courtecuisse R, Duhem B (2011) Guide des Champignons de France et d’Europe. Delachaux et Niestlé, Paris
  99. Cripps CL (1997) The genus Inocybe in Montana aspen stands. Mycologia 89:670–688CrossRefGoogle Scholar
  100. Crous PW, Braun U (2003) Mycosphaerella and its anamorphs: 1. Names published in Cercospora and Passalora. CBS biodiversity series no Centraalbureau voor Schimmelcultures, Utrecht
  101. Crous PW, Slippers B, Wingfield MJ, Rheeder J, Marasas WFO, Philips AJL, Alves A, Burgess TI, Barber PA, Groenewald JZ (2006) Phylogenetic lineages in the Botryosphaeriaceae. Stud Mycol 55:235–253PubMedPubMedCentralCrossRefGoogle Scholar
  102. Crous PW, Braun U, Groenewald JZ (2007) Mycosphaerella is polyphyletic. Stud Mycol 58:1–3PubMedPubMedCentralCrossRefGoogle Scholar
  103. Crous PW, Schoch CL, Hyde KD, Wood AR, Gueidan C, de Hoog GS, Groenewald JZ (2009) Phylogenetic lineages in the Capnodiales. Stud Mycol 64:17–47PubMedPubMedCentralCrossRefGoogle Scholar
  104. Crous PW, Summerell BA, Shivas RG, Romberg M, Mel’nik VA, Verkley GJM, Groenewald JZ (2011) Fungal planet description sheets: 92–106. Persoonia 27:130–162PubMedPubMedCentralCrossRefGoogle Scholar
  105. Crous PW, Quaedvlieg W, Sarpkaya K, Can C, Erkılıç A (2013a) Septoria-like pathogens causing leaf and fruit spot of pistachio. IMA Fungus 4:187–199PubMedPubMedCentralCrossRefGoogle Scholar
  106. Crous PW, Braun U, Hunter GC, Wingfield MJ, Verkley GJ, Shin HD, Nakashima C, Groenewald JZ (2013b) Phylogenetic lineages in Pseudocercospora. Stud Mycol 75:37–114PubMedCrossRefGoogle Scholar
  107. Crous PW, Wingfield MJ, Schumacher RK, Summerell BA, Giraldo A, Gené J, Guarro J, Wanasinghe DN, Hyde KD, Camporesi E, Garethjones EB (2014) Fungal planet description sheets: 281–319. Persoonia 33:212–289PubMedPubMedCentralCrossRefGoogle Scholar
  108. Crous PW, Wingfield MJ, Guarro J, Hernández-Restrepo M, Sutton DA, Acharya K, Barber PA, Boekhout T, Dimitrov RA, Dueñas M, Dutta AK (2015a) Fungal planet description sheets: 320–370. Persoonia 34:167–266PubMedPubMedCentralCrossRefGoogle Scholar
  109. Crous PW, Carris LM, Giraldo A, Groenewald JZ, Hawksworth DL, Hernández-Restrepo M, Jaklitsch WM, Lebrun M-H, Schumacher RK, Stielow JB (2015b) The genera of fungi-fixing the application of the type species of generic names-G 2: AllantophomopsisLatoruaMacrodiplodiopsisMacrohilumMilospiumProtostegiaPyriculariaRobillardaRotulaSeptoriellaTorula, and Wojnowicia. IMA Fungus 6:163–198PubMedPubMedCentralCrossRefGoogle Scholar
  110. Dai DQ, Phookamsak R, Wijayawardene NN, Li WJ, Bhat DJ, Xu JC, Taylor JE, Hyde KD, Chukeatirote E (2017) Bambusicolous fungi. Fungal Divers 82:1–105CrossRefGoogle Scholar
  111. Dai YC (2012) Polypore diversity in China with an annotated checklist of Chinese polypores. Mycoscience 53:49–80CrossRefGoogle Scholar
  112. 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 11:287–302CrossRefGoogle Scholar
  113. Dai YC, Xue HJ, Vlasák J, Rajchenberg M, Wang B, Zhou LW (2014) Phylogeny and global diversity of Polyporus group Melanopus (Polyporales, Basidiomycota). Fungal Diver 64:133–144CrossRefGoogle Scholar
  114. Damm U, Woudenberg JHC, Cannon PF, Crous PW (2009) Colletotrichum species with curved conidia from herbaceous hosts. Fungal Divers 39:45–87Google Scholar
  115. Daranagama DA, Camporesi E, Tian Q, Liu X, Chamyuang S, Stadler M, Hyde KD (2015) Anthostomella is polyphyletic comprising several genera in Xylariaceae. Fungal Divers 73:203–238CrossRefGoogle Scholar
  116. Daranagama DA, Jones EBG, Liu XZ, To-anun C, Stadler M, Hyde KD (2016) Mycosphere Essays 13—do xylariaceous macromycetes make up most of the Xylariomycetidae? Mycosphere 7:582–601Google Scholar
  117. Das K, Dentinger BTM (2015) Austroboletus olivaceoglutinosus, a new mushroom species from Sikkim, India with a distinctive green, glutinous pileus. Kew Bull 70:15CrossRefGoogle Scholar
  118. Das K, Hembrom ME, Parihar A, Mishra D, Sharma JR (2014) Strobilomyces polypyramis—rediscovery of a wild mushroom from Sikkim, India. Indian J Plant Sci 3(2):13–18Google Scholar
  119. De Gruyter J, Noordeloos ME (1992) Contributions towards a monograph of Phoma (Coelomycetes)-I. 1. Section Phoma: taxa with very small conidia in vitro. Persoonia 15:71–92Google Scholar
  120. De Gruyter J, Noordeloos ME, Boerema GH (1998) Contributions towards a monograph of Phoma (Coelomycetes)—I. 3. Section Phoma: taxa with conidia longer than 7 μm. Persoonia 16:471–490Google Scholar
  121. De Gruyter J, Aveskamp MM, Woudenberg JHC, Verkley GJM, Groenewald JZ, Crous PW (2009) Molecular phylogeny of Phoma and allied anamorph genera: towards a reclassification of the Phoma complex. Mycol Res 113:508–519PubMedCrossRefGoogle Scholar
  122. De Gruyter J, Woudenberg JHC, Aveskamp MM, Verkley GJM, Groenewald JZ, Crous PW (2010) Systematic reappraisal of species in Phoma section ParaphomaPyrenochaeta and Pleurophoma. Mycologia 102:1066–1081PubMedCrossRefGoogle Scholar
  123. De Gruyter J, Woudenberg JHC, Aveskamp MM, Verkley GJM, Groenewald JZ, Crous PW (2013) Redisposition of phoma-like anamorphs in Pleosporales. Stud Mycol 75:1–36PubMedCrossRefGoogle Scholar
  124. de Hoog GS, Hermanides-Nijhof EJ (1977) The black yeasts and allied hyphomycetes. Mycologia 69:1242–1244Google Scholar
  125. de Hoog GS, Vicente VA, Najafzadeh MJ, Harrak MJ, Badali H, Seyedmousavi S (2011) Waterborne Exophiala species causing disease in coldblooded animals. Persoonia 27:46–72PubMedPubMedCentralCrossRefGoogle Scholar
  126. De Notaris G (1844) Cenno sulla tribu dei pirenomiceti sferiacei e descrizione di alcuni nuovi generi. Giornale Botanico Italiano 1:322–335Google Scholar
  127. de Souza CAF, Lima DX, Gurgel LMS, Santiago ALCM (2016) Coprophilous Mucorales (ex Zygomycota) from three areas in the semi-arid of Pernambuco. Brazil. Braz J Microbiol 48(1):1–8Google Scholar
  128. Dennis RWG (1951) Some tropical American Agaricaceae referred by Berkeley and Montagne to Marasmius, Collybia or Heliomyces. Kew Bull 6(3):387–410CrossRefGoogle Scholar
  129. Desjardin DE (1989) The Genus Marasmius from the southern Appalachian Mountains. Doctoral dissertations, University of Tennessee, Knoxville
  130. Desjardin DE, Retnowati A, Horak E (2000) Agaricales of Indonesia: 2. A preliminary monograph of Marasmius from Java and Bali. Sydowia 52:92–193Google Scholar
  131. Desjardin DE, Wood MG, Stevens FA (2015) California mushrooms. Timber Press, Portland, OregonGoogle Scholar
  132. Diedicke (1912) Kryptogamen-Flora der Mark Brandenburg 9(5):206
  133. Dissanayake AJ, Camporesi E, Hyde KD, Phillips AJL, Fu CY, Yan JY, Li XH (2016) Dothiorella species associated with woody hosts in Italy. Mycosphere 7:51–63Google Scholar
  134. Dissing H (1966) genus Helvella in Europe with special emphasis on the species found in Norden. Dansk Botanisk Arkiv. 25(1):1–172Google Scholar
  135. Dissing H (1979) Helvella papuensis, a new species from Papua New Guinea. Sydowia Annales Mycologici, Beihefte 8:156–161Google Scholar
  136. Doilom M, Shuttleworth L, Roux J, Chukeatirote E, Hyde KD (2014) Barriopsis tectonae sp. nov. a new species of Botryosphaeriaceae from Tectona grandis (teak) in Thailand. Phytotaxa 176:081–091CrossRefGoogle Scholar
  137. Doilom M, Dissanayake AJ, Wanasinghe DN, Boonmee S, Liu JK, Bhat DJ, Taylor JE, Bahkali AH, McKenzie EHC, Hyde KD (2017) Microfungi on Tectona grandis (teak) in Northern Thailand. Fungal Divers 82:107–182CrossRefGoogle Scholar
  138. Donk MA (1949) New and revised nomina generica conservanda proposed for Basidiomycetes (Fungi). Bull Jard Bot 18:83–168Google Scholar
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