Skip to main content

Advertisement

SpringerLink
Log in

Families of Sordariomycetes

  • Published:
Fungal Diversity Aims and scope Submit manuscript

Abstract

Sordariomycetes is one of the largest classes of Ascomycota that comprises a highly diverse range of fungi characterized mainly by perithecial ascomata and inoperculate unitunicate asci. The class includes many important plant pathogens, as well as endophytes, saprobes, epiphytes, coprophilous and fungicolous, lichenized or lichenicolous taxa. They occur in terrestrial, freshwater and marine habitats worldwide. This paper reviews the 107 families of the class Sordariomycetes and provides a modified backbone tree based on phylogenetic analysis of four combined loci, with a maximum five representative taxa from each family, where available. This paper brings together for the first time, since Barrs’ 1990 Prodromus, descriptions, notes on the history, and plates or illustrations of type or representative taxa of each family, a list of accepted genera, including asexual genera and a key to these taxa of Sordariomycetes. Delineation of taxa is supported where possible by molecular data. The outline is based on literature to the end of 2015 and the Sordariomycetes now comprises six subclasses, 32 orders, 105 families and 1331 genera. The family Obryzaceae and Pleurotremataceae are excluded from the class.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9
Fig. 10
Fig. 11
Fig. 12
Fig. 13
Fig. 14
Fig. 15
Fig. 16
Fig. 17
Fig. 18
Fig. 19
Fig. 20
Fig. 21
Fig. 22
Fig. 23
Fig. 24
Fig. 25
Fig. 26
Fig. 27
Fig. 28
Fig. 29
Fig. 30
Fig. 31
Fig. 32
Fig. 33
Fig. 34
Fig. 35
Fig. 36
Fig. 37
Fig. 38
Fig. 39
Fig. 40
Fig. 41
Fig. 42
Fig. 43
Fig. 44
Fig. 45
Fig. 46
Fig. 47
Fig. 48
Fig. 49
Fig. 50
Fig. 51
Fig. 52
Fig. 53
Fig. 54
Fig. 55
Fig. 56
Fig. 57
Fig. 58
Fig. 59
Fig. 60
Fig. 61
Fig. 62
Fig. 63
Fig. 64
Fig. 65
Fig. 66
Fig. 67
Fig. 68
Fig. 69
Fig. 70
Fig. 71
Fig. 72
Fig. 73
Fig. 74
Fig. 75
Fig. 76
Fig. 77
Fig. 78
Fig. 79
Fig. 80
Fig. 81
Fig. 82
Fig. 83
Fig. 84
Fig. 85
Fig. 86
Fig. 87
Fig. 88
Fig. 89
Fig. 90
Fig. 91
Fig. 92
Fig. 93
Fig. 94
Fig. 95
Fig. 96
Fig. 97
Fig. 98
Fig. 99
Fig. 100
Fig. 101
Fig. 102
Fig. 103
Fig. 104
Fig. 105
Fig. 106
Fig. 107
Fig. 108
Fig. 109
Fig. 110
Fig. 111
Fig. 112
Fig. 113
Fig. 114
Fig. 115
Fig. 116
Fig. 117
Fig. 118
Fig. 119
Fig. 120
Fig. 121
Fig. 122
Fig. 123
Fig. 124
Fig. 125
Fig. 126
Fig. 127
Fig. 128
Fig. 129
Fig. 130
Fig. 131
Fig. 132
Fig. 133
Fig. 134
Fig. 135
Fig. 136
Fig. 137
Fig. 138
Fig. 139
Fig. 140
Fig. 141
Fig. 142
Fig. 143
Fig. 144
Fig. 145
Fig. 146
Fig. 147
Fig. 148
Fig. 149
Fig. 150
Fig. 151
Fig. 152
Fig. 153
Fig. 154
Fig. 155
Fig. 156
Fig. 157

Similar content being viewed by others

References

  • Abdel-Wahab MA, Abdel-Aziz FA, Mohamed SS, Abdel-Aziz AE (2011) Annulatascus nilensis sp. nov., a new freshwater ascomycete from the River Nile, Egypt. IMA Fungus 2:1–6

    Article  PubMed  PubMed Central  Google Scholar 

  • Abdel-Wahab MA, Pang KL, Nagahama T, Abdel-Aziz FA, Jones EBG (2010) Phylogenetic evaluation of anamorphic species of Cirrenalia and Cumulopsora with the description of eight new genera and four new species. Mycol Prog 9:537–558

    Article  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 

  • Ahmed SA, Khan Z, Wang XW, Moussa TA, Al-Zahrani HS, Almaghrabi OA, de Hoog GS (2015) Chaetomium-like fungi causing opportunistic infections in humans: a possible role for extremotolerance. Fungal Divers 76:1–16

    Google Scholar 

  • Ainsworth GC (ed) (1971) Ainsworth & Bisby’s dictionary of the fungi, 6th edn. CABI, Kew

    Google Scholar 

  • Ainsworth GC, Bisby GR (1954) A dictionary of the fungi, 4th edn. The Commonwealth Mycological Institute, Kew

    Google Scholar 

  • Alexopoulos CJ (1962) Introductory mycology, 2nd edn. Wiley, New York, 613 p

    Google Scholar 

  • Alvarez E, Llano GA, Loke JB, Chacon MI (2012) Characterization of Thielaviopsis paradoxa isolates from Oil Palms in Colombia, Ecuador and Brazil. J Phytopathol 160:690–700

    Article  CAS  Google Scholar 

  • Ames LM (1961) A monograph of the Chaetomiaceae. US Army Res Dev Ser, no. 2. Washington, D.C

  • Anagnostakis SL (1987) Chestnut blight: the classical problem of an introduced pathogen. Mycologia 79:23–37

    Article  Google Scholar 

  • Anderson F, Bianchinotti VA (1996) New species of Bartalinia Tassi (Deuteromycotina, Coelomycetes). Mycotaxon 60:191–200

    Google Scholar 

  • Andersson K, Eriksson OE, Landvik S (1995) Boliniaceae transferred to Sordariales (Ascomycota). Syst Ascomycetum 14:1–16

    CAS  Google Scholar 

  • Andrianova TV, Minter DW (2007) New species of Bartalinia and Septoriella from the Altai Mountains (Russia). Mycotaxon 101:297–313

    Google Scholar 

  • Aptroot A (1991) A monograph of the Pyrenulaceae (excluding Anthracothecium and Pyrenula) and the Requienellaceae, with notes on the Pleomassariaceae, the Trypetheliaceae, and Mycomicrothelia (lichenized and non-lichenized ascomycetes). Bibl Lichenologica 44:1–178

    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 YY, Monika CD, 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, Lumbsch HT, Matsumura M, Moncada B, Moncada S, Parnmen S, de Azevedo Santiago ALCM, Sommai S, Song Y, de Souza CAF, de Souza-Motta CM, Su HY, Suetrong S, Wang Y, Wei SF, 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 (2015) Fungal diversity notes 111–252—taxonomic and phylogenetic contributions to fungal taxa. Fungal Divers 75(1):248

  • Arzanlou M, Torbati M, Khodaei S (2013a) Plectosphaerella cucumerina on bamboo in Iran. Mycosphere 4:627–631

    Google Scholar 

  • Arzanlou M, Torbati M, Khodaei S (2013b) Phenotypic and molecular characterization of Plectosphaerella cucumerina on bamboo from Iran. Mycosphere 4:647–651

    Google Scholar 

  • Asgari B, Zare R (2006) Two new Coniochaeta species from Iran. Nova Hedwig 82:227–236

    Article  Google Scholar 

  • Asgari B, Zare R (2011a) The genus Chaetomium in Iran, a phylogenetic study including six new species. Mycologia 103:863–882

    Article  PubMed  Google Scholar 

  • Asgari B, Zare R (2011b) A contribution to the taxonomy of the genus Coniocessia (Xylariales). Mycol Prog 10:189–206

    Article  Google Scholar 

  • Asgari B, Zare R, Gams W (2007) Coniochaeta ershadii, a new species from Iran, and a key to well-documented Coniochaeta species. Nova Hedwig 84:175–187

    Article  Google Scholar 

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

    Google Scholar 

  • Barr ME (1975) Pestalosphaeria, a new genus in the Amphisphaeriaceae. Mycologia 67:187–194

    Article  Google Scholar 

  • Barr ME (1976a) Buergenerula and the PhysosporelIaceae. Mycologia 68:611–621

    Article  Google Scholar 

  • Barr ME (1976b) Perspectives in the Ascomycotina. Mem N Y Bot Gard 28:1–8

    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 (1983) The ascomycete connection. Mycologia 75:1–13

    Article  Google Scholar 

  • Barr ME (1985) Notes on the Calosphaeriales. Mycologia 77:549–565

    Article  Google Scholar 

  • Barr ME (1989) Clypeosphaeria and the Clypeosphaeriaceae. Syst Ascomycetum 8:1–8

    Google Scholar 

  • Barr ME (1990) Prodromus to nonlichenized, pyrenomycetous members of class Hymenoascomycetes. Mycotaxon 39:98–100

  • Barr ME (1994) Notes on the Amphisphaeriaceae and related families. Mycotaxon 51:191–224

  • Barr ME, Cannon PF (1994) Calosphaeriales, Clavicipitales, Coryneliales, Diaporthales, Diatrypales, Halosphaeriales, Hypocreales, Meliolales, Ophiostomatales, Phyllachorales, Sordariales, Trichosphaeriales, and Xylariales. In: Hawksworth DL (ed) Ascomycete systematics. Problems and perspectives in the nineties. Nato ASI Series. Series A: Life Sciences, vol 269. Plenum Press

  • Barr ME, Rogers JD, Ju YM (1993) Revisionary studies in the Calosphaeriaceae. Mycotaxon 48:529–535

    Google Scholar 

  • Barron GL (1991) A new genus, Rotiferophthora, to accommodate the Diheterospora-like endoparasites of rotifers. Can J Bot 69:494–502

    Article  Google Scholar 

  • Barron GL, Cain RF, Gilman JC (1961) The genus Microascus. Can J Bot 39:1609–1631

    Article  Google Scholar 

  • Benny GL, Kimbrough JW (1980) A synopsis of the orders and families of Plectomycetes with keys to genera. Mycotaxon 12:1–91

    Google Scholar 

  • Berbee ML, Taylor JW (1992) Detecting morphological convergence in true fungi, using 18S rRNA gene sequence data. Biosystems 28:117–125

    Article  CAS  PubMed  Google Scholar 

  • Berlese AN (1900) Icones Fungorum. Pyrenomycetes. Sphaeriaceae. Allantosporae. Patavii 3:1–120

  • Bessy EA (1950) Morphology and taxonomy of fungi. Blakiston Co., Philadelphia, 791p

    Book  Google Scholar 

  • Bhat DJ, Kendrick WB (1993) Twenty-five new conidial fungi from the Western Ghats and the Andaman Islands (India). Mycotaxon 49:19–90

    Google Scholar 

  • Bills GF, González-Menéndez V, Martín J, Platas G, Fournier J, Peršoh D, Stadler M (2012) Hypoxylon pulicicidum sp. nov.(Ascomycota, Xylariales), a pantropical insecticide-producing endophyte. PLoS One 7(10):e46687

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Bischoff JF, White JF Jr (2003) The plant-infecting clavicipitaleans. In: White JF Jr, Bacon CW, Hywel-Jones NL, Spatafora JW (eds) Clavicipitalean fungi: evolutionary biology, chemistry, biocontrol, and cultural impacts. Marcel Decker, Inc, New York, pp 125–150

  • Bitzer J, Læssøe T, Fournier J, Kummer V, Decock C, Tichy HV, Piepenbring M, Peršoh D, Stadler M (2008) Affinities of Phylacia and the daldinoid Xylariaceae, inferred from chemotypes of cultures and ribosomal DNA sequences. Mycol Res 112:251–270

    Article  CAS  PubMed  Google Scholar 

  • Boonyuen N, Chuaseeharonnachai C, Suetrong S, Sri-indrasutdhi V, Sivichai S, Jones EBG, Pang KL (2011) Savoryellales (Hypocreomycetidae, Sordariomycetes): a novel lineage of aquatic ascomycetes inferred from multiple-gene phylogenies of the genera Ascotaiwania, Ascothailandia, and Savoryella. Mycologia 103:1351–1371

    Article  PubMed  Google Scholar 

  • Boonyuen N, Sri-indrasutdhi V, Suetrong S, Sivichai S, Jones EBG (2012) Annulatascus aquatorba sp. nov., a lignicolous freshwater ascomycete from Sirindhorn peat swamp forest, Narathiwat, Thailand. Mycologia 104:746–757

    Article  PubMed  Google Scholar 

  • Booth C (1957) Studies on pyrenomycetes I. and II. Mycol Pap 68:1–27

    Google Scholar 

  • Brasier CM (1991) Ophiostoma novo-ulmi sp. nov. causative agent of the current Dutch elm disease pandemics. Mycopathologia 115:151–161

    Article  Google Scholar 

  • Brefeld O (1895) Hemibasidii. Brandpilze III. Cultur der Brandpilzen in Nährlösungen. Untersuchungen aus dem Gesammtgebiete der Mykologie 12:99–236

    Google Scholar 

  • Breitenbach J, Kränzlin F (1984) Champignons de Suisse. Ascomycètes. Ed. Mykologia, Lucerne: 310

  • Bright DE, Torres JA (2006) Studies on West Indian Scolytidae (Coleoptera). A review of the Scolytidae of Puerto Rico, USA, with descriptions of one new genus, fourteen new species and notes on new synonymy. Koleopterol Rundsch 76:389–428

    Google Scholar 

  • Bussaban B, Lumyong S, Lumyong P, Seelanan T, McKenzie EHC, Hyde KD (2005) Molecular and morphological characterization of Pyricularia and allied genera. Mycologia 97:1002–1011

    Article  CAS  PubMed  Google Scholar 

  • Cai L, Hyde KD, Tsui CKM (2006a) Genera of freshwater fungi. Fungal Divers Res Ser 18:1–261

    Google Scholar 

  • Cai L, Jeewon R, Hyde KD (2006b) Molecular systematics of Zopfiella and allied genera: evidence from multi-gene sequence analyses. Mycol Res 110:359–368

    Article  CAS  PubMed  Google Scholar 

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

    Article  CAS  PubMed  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 

  • Calatayud V, Aguirre-Hudson B (2001) Observations on the genus Cresporhaphis (Trichosphaeriaceae), with a key to the known species, and C. ulmi sp. nov. Mycol Res 105:122–126

    Article  Google Scholar 

  • Campbell J, Shearer CA (2004) Annulusmagnus and Ascitendus, two new genera in the Annulatascaceae. Mycologia 96:822–833

    Article  PubMed  Google Scholar 

  • Campbell J, Anderson JL, Shearer CA (2003) Systematics of Halosarpheia based on morphological and molecular data. Mycologia 95(3):530–552

    Article  CAS  PubMed  Google Scholar 

  • Campbell J, Inderbitzin P, Kohlmeyer J, Volkmann-Kohlmeyer B (2009) Koralionastetales, a new order of marine Ascomycota in the Sordariomycetes. Mycol Res 113:373–380

    Article  CAS  PubMed  Google Scholar 

  • Campbell J, Volkmann-Kohlmeyer B, Gräfenhan T, Spatafora JW, Kohlmeyer J (2005) A re-evaluation of Lulworthiales: relationships based on 18S and 28S rDNA. Mycol Res 109:556–568

    Article  CAS  PubMed  Google Scholar 

  • Cannon PF (1988) Proposal to merge the Phyllachorales with the Diaporthales, with a new family structure. Syst Ascomycetum 7:23–43

    Google Scholar 

  • Cannon PF (1991) A revision of Phyllachora and some similar genera on the host family Leguminosae. Mycol Pap 163:302

    Google Scholar 

  • Cannon PF (1994) The newly recognized family Magnaporthaceae and its inter relationships. Syst Ascomycetum 13:25–42

    Google Scholar 

  • Cannon PF (1995) Studies on fungi with isthmoid ascospores: the genus Vialaea, with the description of the new family Vialaeaceae. Mycol Res 99:367–373

    Article  Google Scholar 

  • Cannon PF, Buddie AG, Bridge PD, de Neergaard E, Lübeck M, Askar MM (2012a) Lectera, a new genus of the Plectosphaerellaceae for the legume pathogen Volutella colletotrichoides. MycoKeys 3:23–36

    Article  Google Scholar 

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

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cannon PF, Hawksworth DL (1982) A re-evaluation of Melanospora Corda and similar pyrenomycetes, with a revision of the British species. Bot J Linn Soc 84:115–160

    Article  Google Scholar 

  • Cannon PF, Kirk PM (2007) Fungal Families of the World CABI Publishing Series, CABI

  • Carlucci A, Raimondo ML, Santos J, Phillips AJL (2012) Plectosphaerella species associated with root and collar rots of horticultural crops in southern Italy. Persoonia 28:34–48

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Carmaran CC, Romero AI, Giussani LM (2006) An approach towards a new phylogenetic classification in Diatrypaceae. Fungal Divers 23:67–87

    Google Scholar 

  • Carroll G, Munk A (1964) Studies on lignicolous Sordariaceae. Mycologia 56:77–98

    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 

  • Castlebury LA, Rossman AY, Sung GH, Hyten AS, Spatafora JW (2004) Multigene phylogeny reveals new lineage for Stachybotrys chartarum, the indoor air fungus. Mycol Res 108:864–872

    Article  CAS  PubMed  Google Scholar 

  • Cavaliere AR, Johnson TW (1965) A new marine Ascomycete from Australia. Mycologia 57:927–932

    Article  Google Scholar 

  • Cavara F (1892) Contributzione alla micologia lombarda. Atti Ist Bot Univer Lab Crittogam Pavia Ser 2:207–292

    Google Scholar 

  • Cavara F (1894) Ulteriore contribuzione alla micologia lombarda. Atti dell’Ist Bot Univ e Lab Crittogamico Pavia 3:313–350

    Google Scholar 

  • Cesati V, De Notaris G (1863) Schema di classificazione degle sferiacei italici aschigeri piu’ o meno appartenenti al genere Sphaeria nell’antico significato attribuitoglide Persono. Commentario della Soc Crittogamologica Ital 1:177–420

    Google Scholar 

  • Chadefaud M (1960) Les végétaux non vasculaires (Cryptogamie). In: Chadefaud M, Emberger L (eds) Traité de botanique systématique. Tome I, Masson et Cie, Paris, pp 613–616

    Google Scholar 

  • Chaudhary P, Campbell J, Hawksworth DL, Sastry KN (2006) Vittatispora, a new melanosporaceous genus from Indian soil. Mycologia 98:460–467

    Article  PubMed  Google Scholar 

  • 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 

  • Chaverri P, Salgado C, Hirooka Y, Rossman A, Samuels G (2011) Delimitation of Neonectria and Cylindrocarpon (Nectriaceae, Hypocreales, Ascomycota) and related genera with Cylindrocarpon-like anamorphs. Stud Mycol 68:35–56

    Article  PubMed  PubMed Central  Google Scholar 

  • Chaverri P, Samuels GJ, Hodge KT (2005) The genus Podocrella and its nematode-killing anamorph Harposporium. Mycologia 97:433–443

    Article  CAS  PubMed  Google Scholar 

  • Checa J, Blanco MN, Moreno G (2013) Contributions to the family Thyridiaceae. New data on Sphaeria mutabilis. Mycotaxon 125:149–164

    Article  Google Scholar 

  • Checa J, Blanco MN, Moreno G, Alvarado P, Esquivel E (2014) Amplistroma erinaceum, a new species and its anamorphfrom Panama. Mycol Prog 13:277–283

    Article  Google Scholar 

  • Cheewangkoon R, Groenewald JZ, Verkley GJM, Hyde KD, Wingfield MJ, Gryzenhout M, Summerell BA, Denman S, Toanun C, Crous PW (2010) Re-evaluation of Cryptosporiopsis eucalypti and Cryptosporiopsis-like species occurring on Eucalyptus leaves. Fungal Divers 44:89–105

    Article  Google Scholar 

  • Chen SF, van Wyk M, Roux J, Wingfield MJ, Xie YJ, Zhou XD (2013) Taxonomy and pathogenicity of Ceratcystis species on Eucalyptus trees in South China, including C. chinaeucensis sp. nov. Fungal Divers 58:267–279

    Article  Google Scholar 

  • Chen W, Shearer CA, Crane JL (1999) Phylogeny of Ophioceras spp. based on morphological and molecular data. Mycologia 91:84–94

    Article  CAS  Google Scholar 

  • Chesters CGC (1935) Studies on British Pyrenomycetes: I. The life histories of three species of Cephalotheca Fuck. Trans Brit Mycol Soc 19:261–279

    Article  Google Scholar 

  • Chesters CGC, Greenhalgh GN (1964) Geniculosporium serpens gen. et sp. nov., the imperfect morph of Hypoxylon serpens. Trans Br Mycol Soc 47:393–401

    Article  Google Scholar 

  • Chi PK, Jiang ZD, Zeng L (2002) Two new species of fungi on Bromeliaceae. Mycosystema 21:23–24

    Google Scholar 

  • Chlebicki A, Krzyzanowska J (1995) Notes on pyrenomycetes and coelomycetes from Poland 3. Diatrype subaffixa, a new species for Europe. Sydowia 47:11–31

  • Clements FE, Shear CL (1931) The Genera of Fungi. H. W. Wilson Co, New York

    Google Scholar 

  • Conway KE, Barr ME (1977) Classification of Ophioceras dolichostomum. Mycotaxon 5:376–380

    Google Scholar 

  • Cooke MC (1887) New Australian fungi. Grevillea 16:1–6

    Google Scholar 

  • Coppin E, Debuchy R, Arnaise S, Picard M (1997) Mating-types and sexual development in filamentous ascomycetes. Myicrobiol Mol Biol Rev 61:411–428

    CAS  Google Scholar 

  • Corda ACI (1831) Die Pilze Deutschlands. In: Sturm J (ed) Deutschlands Flora in Abbildungen nach der Natur mit Beschreibungen. Sturm, Nürnberg vol. 3, Abt. 12:33–64, tab. 21–32

  • Corda ACJ (1833) Deutschlands Flora, Abt. III. Die Pilze Deutschlands 3–13:65–96

    Google Scholar 

  • Corda ACJ (1837) Icones fungorum hucusque cognitorum. Vol. 1. J.G. Calve, Prague 32

  • Corlett M (1963) The developmental morphology of two species of Microascus. Can J Bot 41:253–266

    Article  Google Scholar 

  • Corlett M (1966) Developmental studies in the Microascaceae. Can J Bot 44:79–88

    Article  Google Scholar 

  • Crous PW, Carris LM, Giraldo A, Groenewald JZ, Hawksworth DL, Hernández-Restrepo M, Jaklitsch WM, Lebrun MH, Schumacher RK, Stielow JB, van der Linde EJ, Vilcāne J, Voglmayr H, Wood AR (2015a) 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, Giraldo A, Hawksworth DL, Robert V, Kirk PM, Guarro J (2014a) The genera of fungi: fixing the application of type species of generic names. IMA Fungus 5:141–160

    Article  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Groenewald JZ (2013) A phylogenetic re-evaluation of Arthrinium. IMA Fungus 4:133–154

    Article  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Groenewald JZ, Himaman W (2007a) Falcocladium thailandicum Crous & Himaman, sp. nov. Fungal Planet: 18

  • Crous PW, Mohammed C, Glen M, Verkley GJ, Groenewald JZ (2007b) Eucalyptus microfungi known from culture. 3. Eucasphaeria and Sympoventuria genera nova, and new species of Furcaspora, Harknessia, Heteroconium and Phacidiella. Fungal Divers 25:19–36

  • Crous PW, Kendrick B, Alfenas AC (1997) New species of hyphomycetes associated with Eucalyptus. S Afr J Bot 63:286–290

    Article  Google Scholar 

  • Crous PW, Knox-Davies PS, Wingfield MJ (1989) Newly-recorded foliage fungi of Eucalyptus spp. in South Africa. Phytophylactica 21:85–88

    Google Scholar 

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

    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 PAS, 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 PTW, Groenewald JZ (2014b) Fungal Planet Description Sheets: 214–280. Persoonia 32:184–306

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Summerell BA, Shivas RG, Carnegie AJ, Groenewald JZ (2012) A re-appraisal of Harknessia (Diaporthales), and the introduction of Harknessiaceae fam. nov. Persoonia 28:49–65

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Crous PW, Wingfield MJ, Alfenas AC, Silviera SF (1994) Cylindrocladium naviculatum sp. nov., and two new vesiculate hyphomycete genera, Falcocladium and Vesicladiella. Mycotaxon 50:441–458

    Google Scholar 

  • Crous PW, Wingfield MJ, Le Roux JJ, Richardson DM, Strasberg D, Shivas RG, Alvarado P, Edwards J, Moreno G, Sharma R, Sonawane MS, Tan YP, Altés A, Barasubiye T, Barnes CW, Blanchette RA, Boertmann D, Bogo A, Carlavilla JR, Cheewangkoon R, Daniel R, de Beer ZW, de Jesús Yáñez-Morales M, Duong TA, Fernández-Vicente J, Geering ADW, Guest DI, Held BW, Heykoop M, Hubka V, Ismail AM, Kajale SC, Khemmuk W, Kolařík M, Kurli R, Lebeuf R, Lévesque CA, Lombard L, Magista D, Manjón JL, Marincowitz S, Mohedano JM, Nováková A, Oberlies NH, Otto EC, Paguigan ND, Pascoe IG, Pérez-Butrón JL, Perrone G, Rahi P, Raja HA, Rintoul T, Sanhueza RMV, Scarlett K, Shouche YS, Shuttleworth LA, Taylor PWJ, Thorn RG, Vawdrey LL, Solano-Vidal R, Voitk A, Wong PTW, Wood AR, Zamora JC, Groenewald JZ (2015c) Fungal planet description sheets: 371–399. Persoonia 35:264–327

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Cruywagen EM, De Beer ZW, Roux J, Wingfield MJ (2010) Three new Graphium species from baobab trees in South Africa and Madagascar. Persoonia 25:61–71

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Dai DQ, Bahkali AH, Li QR, Bhat DJ, Wijayawardene NN, Li WJ, Chukeatirote E, Zhao RL, Xu JC, Hyde KD (2014a) Vamsapriya (Xylariaceae) re-described, with two new species and molecular sequence data. Cryptogam Mycol 35:339–357

    Article  Google Scholar 

  • Dai DQ, Wijayawardene NN, Bhat DJ, Chukeatirote E, Bahkali AH, Zhao RL, Xu JC, Hyde KD (2014b) Pustulomyces gen. nov. accommodated in Diaporthaceae, Diaporthales, as Revealed by Morphology and Molecular Analyses. Cryptogam Mycol 35(1):63–72

    Article  Google Scholar 

  • Damm U, Crous PW, Fourie PH (2008) A fissitunicate ascus mechanism in the Calosphaeriaceae, and novel species of Jattaea and Calosphaeria on Prunus wood. Persoonia 20:39–52

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Damm U, Fourie PH, Crous PW (2010) Coniochaeta (Lecythophora), Collophora gen. nov. and Phaeomoniella species associated with wood necroses of Prunus trees. Persoonia 24:60–80

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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

    Google Scholar 

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

    Article  Google Scholar 

  • De Beer ZW, Seifert KA, Wingfield MJ (2013) The ophiostomatoid fungi: their dual position in the Sordariomycetes. In: Seifert KA, de Beer ZW, Wingfield MJ (eds) The ophiostomatoid fungi: expanding frontiers, CBS Fungal Biodivers Ser 12:1–19

  • De Beer ZW, Duong TA, Barnes I, Wingfield BD, Wingfield MJ (2014) Redefining Ceratocystis and allied genera. Stud Mycol 79:187–219

    Article  PubMed  PubMed Central  Google Scholar 

  • de Hoog GS (1972) The genera Beauveria, lsaria, Tritirachium and Acrodontium. Stud Mycol 1:1–41

    Google Scholar 

  • De Notaris G (1844) Cenni sulla tribù dei Pirenomiceti sferiacei e descrizione di alcuni generi spettanti alla medesima. G Bot Ital 1:322–355

    Google Scholar 

  • Debbab A, Aly AH, Proksch P (2013) Mangrove derived fungal endophytes – a chemical and biological perception. Fungal Divers 61:1–27

    Article  Google Scholar 

  • Dennis RWG (1960) British cup fungi and their allies. An introduction to the Ascomycetes. Bernard Quaritch. Ltd., London, 280p

    Google Scholar 

  • Dennis RWG (1964) Further records of Congo Xylariaceae. Bull Jard Bot l’État à Brux 34:231–241

    Article  Google Scholar 

  • Dettman JR, Jacobson DJ, Taylor JW (2003) A multilocus genealogical approach to phylogenetic species recognition in the model eucaryote Neurospora. Evolution 57:2703–2720

    Article  PubMed  Google Scholar 

  • DiCosmo F, Berch S, Kendrick B (1983) Cylindrotrichum, Chaetopsis and two new genera of Hyphomycetes, Kylindria and Xenokylindria. Mycologia 75:949–973

    Article  Google Scholar 

  • Diehl WW (1950) Balansia and the Balansiae in America. Agric. Monogr. No 4 USDA, Washington

  • Dingley JM (1951a) The Hypocreales of New Zealand. I. Trans Roy Soc N Z 79:55–61

    Google Scholar 

  • Dingley JM (1951b) The Hypocreales of New Zealand. II. The genus Nectria. Trans Roy Soc New Zealand 79:177–202

    Google Scholar 

  • Dingley JM (1952a) The Hypocreales of New Zealand. III. The genus Hypocrea. Trans Roy Soc New Zealand 79:323–337

    Google Scholar 

  • Dingley JM (1952b) The Hypocreales of New Zealand. IV. The genera Calonectria. Gibberella and Thyronectria. Trans Roy Soc New Zealand 79:403–411

    Google Scholar 

  • Dingley JM (1953) The Hypocreales of New Zealand. V. The genera Cordyceps and Torrubilla. Trans Roy Soc New Zealand 81:329–343

    Google Scholar 

  • Dingley JM (1954) The Hypocreales of New Zealand. VI. The genera Hypocrella, Barya, Claviceps and Podonectria. Trans Roy Soc New Zealand 83:643–662

    Google Scholar 

  • Dingley JM (1956) The Hypocreales of New Zealand. VII. A revision of records and species in the Hypocreaceae. Trans Roy Soc New Zealand 81:329–343

    Google Scholar 

  • Doassans JE, Patouillard NT (1892) UneClavariéeentomogène. Rev Mycol Toulouse 14:67–70

    Google Scholar 

  • Doguet G (1957) Organogenie du Mlcroascus stysanophorus (Matt.) Curzi. Bull. Soc Mycol Fr 73:165–178

    Google Scholar 

  • Dreyfuss M (1976) Taxonomische Untersuchungen innerhalb der Gattung Chaetomium. Sydowia 28:50–133

    Google Scholar 

  • Duong LM, Lumyong S, Hyde KD, Jeewon R (2004) Emarcea castanopsidicola gen. et sp. nov. from Thailand, a new xylariaceous taxon based on morphology and DNA sequences. Stud Mycol 50:253–260

    Google Scholar 

  • Earle FS (1901) Collections of Alabama fungi. In: Mohr C (ed) Plant life of Alabama. Contr US Natl, Herb, p 150–263

  • Elbakyan MA (1970) Maloizvestnoe zabolevanie ogurtsov. Trudy. Vsesoyuznyi Nauchno Issledovalel’skii Inslituta Zashchita Rastenii 29:116–120

    Google Scholar 

  • Ellis JB, Halsted BD (1890) New fungi. J Mycol 6:33–35

    Article  Google Scholar 

  • Emmons CW, Dodge BW (1931) The ascosporic stage of species of Scopularlopsls. Mycologia 23:313–331

    Article  Google Scholar 

  • Eriksson OE (1981) The families of bitunicate Ascomycetes. Oper Bot 60:1–209

    Google Scholar 

  • Eriksson OE (1982) Outline of the Ascomycetes—1982. Mycotaxon 15:203–248

    Google Scholar 

  • Eriksson OE (1984) Outline of the ascomycetes. Syst Ascomycetum 3:1–72

    Google Scholar 

  • Eriksson OE (1999) Outline of Ascomycota 1999. Myconet 3:1–88

    Google Scholar 

  • Eriksson OE (2006) Outline of Ascomycota - 2006. Myconet 12:1–82

    Google Scholar 

  • Eriksson OE, Baral HO, Currah RS, Hansen K, Kurtzman CP, Rambold G, Laessøe T. (eds). (2003). Outline of ascomycota - 2003. Myconet 9:1–89

  • Eriksson OE, Hawksworth DL (1985) Outline of the Ascomycetes–1985. Syst Ascomycetum 4:1–79

    Google Scholar 

  • Eriksson OE, Hawksworth DL (1986) Notes on ascomycete systematics. Nos 1–224. Syst Ascomycetum 5:113–174

    Google Scholar 

  • Eriksson OE, Hawksworth DL (1987) Notes on ascomycete systematics. Nos. 225–463. Syst Ascomycetum 6:111–165

    Google Scholar 

  • Eriksson OE, Hawksworth DL (1993) Outline of the ascomycetes-1993. Syst Ascomycetum 12:51–257

    Google Scholar 

  • Eriksson OE, Winka K (1997) Supraordinal taxa of Ascomycota. Myconet 1:1–16

    Google Scholar 

  • Eriksson OE, Yue JZ (1989) An amended description and disposition of the genus Thyridium. Syst Ascomycetum 8:9–16

    Google Scholar 

  • Evans HC, Samson RA (1982) Cordyceps species and their anamorphs pathogenic on ants (Formicidae) in tropical forest ecosystems 1. The Cephalotes (Myrmicinae) complex. Trans Br Mycol Soc 79:431–453

    Article  Google Scholar 

  • Farr DF, Rossman AY (2003) Dwiroopa, a coelomycetous genus with two species. Mycoscience 44:443–446

    Article  Google Scholar 

  • Farr DF, Rossman AY (2016) Fungal databases, systematic mycology and microbiology laboratory, ARS, USDA. Retrieved January 6, 2016, from http://nt.arsgrin.gov/fungaldatabases/

  • Faurel L, Schotter G (1959) Un champignon Ascomycete inedit, type dune nouvelle famille de position systematique critique. C R Hebd Seances Acad Sci 249:150–152

  • Fernández FA, Huhndorf SM (2004) Neotropical pyrenomycetes: Porosphaerella borinquensis sp. nov. and its Pseudobotrytis terrestris anamorph. Fungal Divers 17:11–16

    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 

  • Fitzpatrick HM (1923) Monograph of the Nitschkieae. Mycologia 15:23–44

    Article  Google Scholar 

  • Fries EM (1825) Systema Orbis Vegetabilis. Typographia Acad, Lund 1:1–374

    Google Scholar 

  • Fries EM (1849) Summa Vegetabilium Scandinaviae Sectio posterior. 259–572

  • Fuckel KWGL (1864) Fungi Rhenani exsiccati, Fasc. IX-X, no 801–1000. Hedwigia 3:161–165

    Google Scholar 

  • Fuckel L (1870) Symbolae mycologicae. Beiträge zur Kenntniss der Rheinischen Pilze. Jahrbücher des Nassauischen Vereins für Naturkunde 23–24:1–459

    Google Scholar 

  • Fuckel L (1872) Symbolae mycologicae. Beiträge zur Kenntniss der rheinischen Pilze Erster Nachtrag. Jahrbücher des Nassauischen Vereins für Naturkunde 25–26:287–346

    Google Scholar 

  • Gams W (1971) Tolypocladium, eine Hyphomycetengattung mit geschwollenen Phialiden. Persoonia 6:185–191

    Google Scholar 

  • Gams W (1980) Chaunopycnis alba, gen. et sp.nov., a soil fungus intermediate between Moniliales and Sphaeropsidales. Persoonia 11:75–79

    Google Scholar 

  • Gams W, Jansson HB (1985) The nematode parasite Meriaconiospora Drechsler in pure culture and its classification. Mycotaxon 22:33–38

    Google Scholar 

  • Gams W, Zare R (2001) A revision of Verticillium sect. Prostrata. III. Generic classification. Nova Hedwig 72:329–337

    Google Scholar 

  • Gams W, Zare R (2003) A taxonomic review of the clavicipitaceous anamorphs parasitizing nematodes and other microinvertebrates. Mycol Ser 19:17–74

    Google Scholar 

  • García D, Stchigel AM, Cano J, Calduch M, Hawksworth DL, Guarro J (2006) Molecular phylogeny of Coniochaetales. Mycol Res 110:1271–1289

    Article  PubMed  CAS  Google Scholar 

  • Gäumann E (1964) Die Pilze. Birkhäuser Verlag, Basel 541

  • Geldenhuis MM, Roux J, Montenegro F, De Beer ZW, Wingfield MJ, Wingfield BD (2004) Identification and pathogenicity of Graphium and Pesotum species from machete wounds on Schizolobium parahybum in Ecuador. Fungal Divers 15:135–149

    Google Scholar 

  • Glawe DA, Rogers JD (1984) Diatrypaceae in the Pacific Northwest. Mycotaxon 20:401–460

    Google Scholar 

  • Goh TK, Ho WH, Hyde KD, Whitton SR, Umali TE (1998) New records and species of Canalisporium (Hyphomycetes), with a revision of the genus. Can J Bot 76:142–152

    Google Scholar 

  • Goh TK, Hyde KD (1998) A synopsis of and a key to Diplococcium species, based on the literature, with a description of a new species. Fungal Divers 1:65–83

    Google Scholar 

  • Goidànich G (1935) Schema di una classificazione delle StiIbacee che erano riunite fin’ora nel genere Graphium Corda. Ann Bot 21:40–50

    Google Scholar 

  • Gramaje D, Di Marco S (2015) Identifying practices likely to have impacts on grapevine trunk disease infections: a European nursery survey. Phytopathol Mediterr 54:313–324

    Google Scholar 

  • Gramaje D, Mostert L, Groenewald JZ, Crous PW (2015) Phaeoacremonium: from esca disease to phaeohyphomycosis. Fungal Biol 119(9):759–783

  • Granmo A, Petrini LE (1996) A new species of Lopadostoma, and the anamorph of Biscogniauxia cinereolilacina. Mycol Helv 8:43–50

    Google Scholar 

  • Greville KR (1823–1824) Scottish cryptogamic flora. 2:82–83

  • Grum-Grzhimaylo AA, Debets AJM, van Diepeningen AD, Georgieva ML, Bilanenko EN (2013) Sodiomyces alkalinus, a new holomorphic alkaliphilic ascomycete within the Plectosphaerellaceae. Persoonia 31:147–158

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Grum-Grzhimaylo AA, Georgieva ML, Bondarenko SA, Debets AJ, Bilanenko EN (2016) On the diversity of fungi from soda soils. Fung Divers 76:27–74

    Article  Google Scholar 

  • Grunow A, Hauck F, Limpricht G, Luerssen Ch, Richter P, Winter G (1887) Family Chaetomieae. Rabenh. Krypt.-Fl., Edn 2 (Leipzig) 1.2:153 / http://www.biodiversitylibrary.org/page/1172638#page/164/mode/1up

  • Gryzenhout M, Myburg H, Hodges CS, Wingfield BD, Wingfield MJ (2006) Microthia, Holocryphia and Ursicollum, three new genera on Eucalyptus and Coccoloba for fungi previously known as Cryphonectria. Stud Mycol 55:35–52

    Article  PubMed  PubMed Central  Google Scholar 

  • Guba EF (1961) Monograph of Pestalotia and Monochaetia. Harvard University Press, Cambridge

    Google Scholar 

  • Halsted BD (1890) Some fungus disease of the sweet potato. N J Aes Bull 76:25–27

    Google Scholar 

  • Halsted BD, Fairchild DG (1891) Sweet potato black rot. J Mycol 7:1–11

    Article  Google Scholar 

  • Hamayun M, Khan SA, Khan AL, Afzal M, Lee IJ (2012) Endophytic Cephalotheca sulfurea AGH07 reprograms soybean to higher growth. J Plant Interact 7:301–306

    Article  CAS  Google Scholar 

  • Hanlin RT, Tortolero O (1991) Icones ascomycetum Venezuelae: Phyllachora fusicarpa. Mycotaxon 41:19–26

    Google Scholar 

  • Hara K (1939) Diseases of the rice plant [Ine no byōgai] Ed.2:185

  • Harrington TC, McNew D, Steimel J, Hofstra D, Farrell R (2001) Phylogeny and taxonomy of the Ophiostoma piceae complex and the Dutch Elm Disease fungi. Mycologia 93:111–136

    Article  CAS  Google Scholar 

  • Harveson RM (1999) Evaluation of the parasitic relationship of Melanospora and other allied genera with Fusarium oxysporum. PhD thesis, University of Florida, Gainesville

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

  • Hausner G, Reid J, Klassen GR (1993a) Ceratocystiopsis: a reappraisal based on molecular criteria. Mycol Res 97:625–633

    Article  Google Scholar 

  • Hausner G, Reid J, Klassen GR (1993b) On the phylogeny of Ophiostoma, Ceratocystis s.s., and Microascus, and relationships within Ophiostoma based on partial ribosomal DNA sequences. Can J Bot 71:1249–1265

    Article  CAS  Google Scholar 

  • Hawksworth DL (1985) Problems and prospects in the systematics of the Ascomycotina. Proc Indian Acad (Sci) 94:319–339

  • Hawksworth DL (2012) Managing and coping with names of pleomorphic fungi in a period of transition. Mycosphere 3:143–155

    Article  Google Scholar 

  • Hawksworth DL, Crous PW, Redhead SA, Reynolds DR, Samson RA, Seifert KA, Taylor JW, Wingfield MJ et al (2011) The Amsterdam declaration on fungal nomenclature. IMA Fungus 2:105–112, Mycotaxon 116:491–500

    Article  PubMed  PubMed Central  Google Scholar 

  • Hawksworth DL, Eriksson OE (1986) The names of accepted orders of ascomycetes. Syst Ascomycetum 5:175–184

    Google Scholar 

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

  • Hawksworth DL, Kirk PM, Sutton BC, Pegler DN (1995) Dictionary of the Fungi. 8th Edn. 616

  • Hawksworth DL, Sutton BC, Ainsworth GC (eds) (1983) Ainsworth & Bisby’s Dictionary of the Fungi, 7th edn. CABI, Kew

    Google Scholar 

  • Hawksworth DL, Wells H (1973) Ornamentation on the terminal hairs in Chaetomium kunze ex fr. and some allied genera. Mycol Pap 134:1–24

    Google Scholar 

  • Hedgcock GG (1906) Studies upon some chromogenic fungi which discolor wood. Mo Bot Gard Annu Rep 17:59–114

    Google Scholar 

  • Heiniger U, Rigling D (1994) Biological control of chestnut blight in Europe. Annu Rev Phytopathol 32:581–599

    Article  Google Scholar 

  • Hellwig V, Ju YM, Rogers JD, Fournier J, Stadler M (2005) Hypomiltin, a novel azaphilone from Hypoxylon hypomiltum, and chemotypes in Hypoxylon sect. Hypoxylon as inferred from analytical HPLC profiling. Mycol Prog 4:39–54

    Article  Google Scholar 

  • Hernández-Restrepo M, Gené J, Mena-Portales J, Cano J, Madrid H, Castañeda-Ruiz RF, Guarro J (2014) New species of Cordana and epitypification of the genus. Mycologia 106:723–734

    Article  PubMed  Google Scholar 

  • Hernández-Restrepo M, Groenewald JZ, Crous PW (2015a) Neocordana gen. nov., the causal organism of Cordana leaf spot on banana. Phytotaxa 205:229–238

    Article  Google Scholar 

  • Hernández-Restrepo M, Groenewald JZ, Crous PW (2015b) Taxonomic and phylogenetic re-evaluation of Microdochium, Monographella and Idriella. Persoonia 36:57–82

    Google Scholar 

  • Hernández-Restrepo M, Silvera-Simón C, Mena-Portales J, Mercado-Sierra Á, Guarro J, Gené J (2012) Three new species and a new record of Diplococcium from plant debris in Spain. Mycol Prog 11:191–199

    Article  Google Scholar 

  • Hibbett DS, Binder M, Bischoff JF, Blackwell M, Cannon PF, Ericksson OE, Huhndorf S, James T, Kirk PM, Lücking R, Lumbsch HT, 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, Dai YC, Gams W, Geiser DM, Griffith GW, Gueidan C, Hawksworth DL, Hestmark G, Hosaka K, Humber RA, Hyde KD, Ironside JE, Kõljalg U, Kurtzman CP, Larsson KH, Litchward R, Longore J, Miadlikowska J, Miller A, Moncalvo JM, Mozley-Standridge S, Oberwinkler F, Parmasto E, Reeb V, Rogers JD, Roux C, Ryvarden L, Sampaio JP, Schüssler 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 higherlevel phylogenetic classification of the Fungi. Mycol Res 111:509–547

    Article  PubMed  Google Scholar 

  • Hilber R, Hilber O (2002) The genus Lasiosphaeria and allied taxa. Germany: Publ. By the authors. 9 p., 7 pl

  • Hirooka Y, Kawaradani M, Sato T (2014) Description of Gibellulopsis chrysanthemi sp. nov. from leaves of garland chrysanthemum. Mycol Prog 13:13–19

    Article  Google Scholar 

  • Hirooka Y, Kobayashi T, Ono T, Rossman AY, Chaverri P (2010) Verrucostoma, a new genus in the Bionectriaceae from the Bonin Islands, Japan. Mycologia 102:418–429

    Article  CAS  PubMed  Google Scholar 

  • Hirooka Y, Rossman AY, Samuels GJ et al (2012) A monograph of Allantonectria, Nectria, and Pleonectria (Nectriaceae, Hypocreales, Ascomycota) and their pycnidial, sporodochial, and synnematous anamorphs. Stud Mycol 71:1–210

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ho WH, Hyde KD (2000) A new family of freshwater ascomycetes. Fungal Divers 4:21–36

    CAS  Google Scholar 

  • Holubová-Jechová V, Sierra AM (1984) Studies on Hyphomycetes from Cuba II. Hyphomycetes from the Isla de la Juventud. Ceská Mykol 38:96–120

    Google Scholar 

  • Hongsanan S, Tian Q, Peršoh D, Zeng XY, Hyde KD, Chomnunti P, Boonmee S, Bahkali AH, Wen TC (2015) Meliolales. Fungal Divers 74:91–144

    Article  Google Scholar 

  • Horst RK (1990) Westcott’s plant disease handbook, 5th edn. AVI Book, USA

    Book  Google Scholar 

  • Hosagoudar VB (2003) Armatellaceae, a new family segregated from the Meliolaceae. Sydowia 55:162–167

    Google Scholar 

  • Hosagoudar VB (2004) Studies on foliicolous fungi – xvi Clasterosporium flagellatum and its teleomorph. Zoos’ Print J 19:1437–1438

    Article  Google Scholar 

  • Hosagoudar VB, Dhivaharan V, Nithyatharani R (2012) Foliicolous fungi of Kodaikanal in Tamil Nadu. Bull Basic Appl Plant Biol 2:94

    Google Scholar 

  • Hsieh HM, Lin CR, Fang MJ, Rogers JD, Fournier J, Lechat C, Ju YM (2010) Phylogenetic status of Xylaria subgenus Pseudoxylaria among taxa of the subfamily Xylarioideae (Xylariaceae) and phylogeny of the taxa involved in the subfamily. Mol Phylogenet Evol 54(3):957–969

    Article  CAS  PubMed  Google Scholar 

  • Hsieh LS, Tzean SS, Wu WJ (1997) The genus Akanthomyces on spiders from Taiwan. Mycologia 89:319–324

    Article  Google Scholar 

  • Huang LH (1976) Developmental morphology of Triangularia backusii (Sordariaceae). Can J Bot 54:250–267

    Article  Google Scholar 

  • Huang B, Wang S, Fan M, Li Z (1999) Two species of Akanthomyces from Dabieshan mountains. Mycosystema 19:172–174

    Google Scholar 

  • Hudson HJ (1963) The perfect state of Nigrospora oryzae. Trans Br Mycol Soc 46:355–360

    Article  Google Scholar 

  • Hughes SJ (1955) Microfungi. I. Cordana, Brachysporium, Phragmocephala. Can J Bot 33:259–268

    Article  Google Scholar 

  • Huhndorf SH, Fernández FA, Miller AN, Lodge DJ (2003) Neotropical ascomycetes 12. Mirannulata samuelsii gen. et sp. nov. and M. costaricensis sp. nov., new taxa from the Carribean and elsewhere. Sydowia 55:172–180

    Google Scholar 

  • Huhndorf SM, Fernández F, Lodge JD (1999) Neotropical Ascomycetes 9. Jobellisia species from Puerto Rico and elsewhere. Sydowia 51:183–196

    Google Scholar 

  • Huhndorf SM, Miller AN, Fernandez FA (2004a) Molecular systematics of the Sordariales: the order and the family Lasiosphaeriaceae redefined. Mycologia 96:368–387

    Article  CAS  PubMed  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Huhndorf SM, Miller AN, Greif M, Samuels MG (2009) Amplistroma gen. nov. and its relation to Walrothiella, two genera with globose ascospores and acrodontium-like anamorphs. Mycologia 101:904–919

    Article  PubMed  Google Scholar 

  • Hujslová M, Kubátová A, Kostovčík M, Blanchette RA, Wilhelm de Beer Z, Chudíčková M, Kolařík M (2014) Three new genera of fungi from extremely acidic soils. Mycol Prog 13:819–831

    Google Scholar 

  • Hulcr J, Kolařík M, Kirkendall LR (2007) A new record of fungus-beetle symbiosis in Scolytodes bark beetles (Scolytinae, Curculionidae, Coleoptera). Symbiosis 43:151–159

    Google Scholar 

  • Hulvova H, Galuszka P, Frebortova J, Frebort I (2013) Parasitic fungus Claviceps as a source for biotechnological production of ergot alkaloids. Biotechnol Adv 31:79–89

    Article  CAS  PubMed  Google Scholar 

  • Humber RA, Rombach MC (1987) Torrubiella ratticaudata sp. nov. (Pyrenomycetes: Clavicipitales) and other fungi from spiders on the Solomon Islands. Mycologia 79:375–382

    Article  Google Scholar 

  • Hyde KD (1992) Tropical Australian freshwater fungi. IV. Halosarpheia aquatica sp. nov., Garethjonesia lacunosispora gen. & sp. nov. and Ophioceras dolichostomum (Ascomycetes). Aust Syst Bot 5:407–414

    Google Scholar 

  • Hyde KD (1993) Fungi from palms. VIII. The genus Myelosperma (Ascomycotina). Sydowia 45:241–245

  • Hyde KD, Cai L, Cannon PF, Crouch JA, Crous PW, Damm U, Goodwin PH, Chen H, Johnston PR, Jones EBG, Liu ZY, McKenzie EHC, Moriwaki J, Noireung P, Pennycook SR, Pfenning LH, Prihastuti H, Sato T, Shivas RG, Tan YP, Taylor PWJ, Weir BS, Yang YL, Zhang JZ (2009a) Colletotrichum—names in current use. Fungal Divers 39:147–182

    Google Scholar 

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

    Google Scholar 

  • Hyde KD, Cannon PF (1999) Fungi causing tar spots on palms. Mycol Pap 175:1–114

    Google Scholar 

  • Hyde KD, Cannon PF, Barr ME (1997) Phaeochoraceae, a new family from palms. Syst Ascomycetum 15:117–120

    Google Scholar 

  • Hyde KD, Fröhlich J, Taylor JE (1998) Fungi from palms. XXXVI. Reflections on unitunicate ascomycetes with apiospores. Sydowia 50:21–80

    Google Scholar 

  • Hyde KD, Goh TK (1998) Fungi on submerged wood in the Riviere St Marie-Louis, The Seychelles. S Afr J Bot 64:330–336

    Article  Google Scholar 

  • Hyde KD, Jones EBG (1989) Intertidal Mangrove Fungi from Brunei. Lautospora gigantea gen. et sp. nov., a New Loculoascomycete from Prop Roots of Rhizophora spp. Bot Mar 32:479–482

    Google Scholar 

  • Hyde KD, Jones EBG (1992) Intertidal mangrove fungi: Pedumispora gen. nov. (Diaporthales). Mycol Res 96:78–80

    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 YX, Lücking 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, Hoog SD, 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, Kang JC, Kong RYC (1996) Fungi from palms. XXX. Notes on Amphisphaeria species described from palms and a description of A. umbrina. Nova Hedwig 63:101–108

    Google Scholar 

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

    Google Scholar 

  • Hyde KD, 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, Pawlowska J, Rintoul TL, Shivas RG, Spies CFJ, Summerell BA, Taylor PWJ, Terhem RB, Udayanga D, Vaghefi N, Walther G, Wilk M, Wrzosek M, Xu JC, Yan JY, Zhou N (2014) One stop shop: backbones trees for important phytopathogenic genera: I. Fungal Divers 67:21–125

    Article  Google Scholar 

  • Hyde KD, Taylor JE, Fröhlich J (2000) Genera of ascomycetes from palms. Fungal Diversity Press, Hong Kong

    Google Scholar 

  • Hyde KD, Wong SW (1999) Ultrastructural studies on the Myelospermaceae fam. Nov., with a new species of Myelosperma. Mycol Res 103(3):347–352

  • Hyde KD, Wong SW (2000) Annulatascus fusiformis sp. nov., a new freshwater ascomycete from the Philippines. Mycologia 92:353–557

    Article  Google Scholar 

  • Illingworth CA, Andrews JH, Bibeau C, Sogin ML (1991) Phylogenetic placementof Atheliabombacina, Aureobasidiumpullulans and Colletotrichum gloeosporioides inferred from sequence comparisons of small subunit ribosomal RNAs. Exp Mycol 15:65–75

    Article  CAS  Google Scholar 

  • Inderbitzin P, Berbee ML (2001) Lollipopaiaminuta from Thailand, a new genus and species of the Diaporthales (Ascomycetes, Fungi) based on morphological and molecular data. Can J Bot 79:1099–1106

    CAS  Google Scholar 

  • Inderbitzin P, Lim SR, Volkmann-kohlmeyer B, Kohlmeyer J, Berbee ML (2004) The phylogenetic position of Spathulospora based on DNA sequences from dried herbarium material. Mycol Res 108:737–748

    Article  CAS  PubMed  Google Scholar 

  • Index fungorum (2016) http://www.indexfungorum.org/Names/Names.asp

  • Ivanová H, Bernadovičová S (2013) Coniochaetaprunicola-first record for Slovakia and Europe. Cent Eur J Biol 8:195–200

    Google Scholar 

  • Jacobs K, Seifert KA, Harrison KJ, Kirisits T (2003) Identity and phylogenetic relationships of ophiostomatoid fungi associated with invasive and native Tetropium species (Coleoptera: Cerambycidae) in Atlantic Canada. Can J Bot 81:316–329

    Article  Google Scholar 

  • Jacobs K, Wingfield MJ (2001) Leptographium Species: tree pathogens, insect associates and agents of blue-stain. American Phytopathological Society Press, St Paul

    Google Scholar 

  • Jacobson DJ, Dettman JR, Powell AJ, Saenz GS, BartonMM HMD, Dvorachek WH, Glass NL, Taylor JW, Natvig DO (2004) Neurospora in temperate forests of western North America. Mycologia 96:66–74

    Article  PubMed  Google Scholar 

  • Jaczewski ALA (1894) Bull Herb Boissier 2:1–663

  • Jaklitsch WM (2015) Savoryellaceae Jaklitsch & Réblová. Index Fungorum 209(1)

  • Jaklitsch WM, Fournier J, Dai DQ, Hyde KD, Voglmayr H (2015) Valsaria and the Valsariales. Fungal Divers 73:159–202

    Article  PubMed  PubMed Central  Google Scholar 

  • Jaklitsch WM, Fournier J, Rogers JD, Voglmayr H (2014) Phylogenetic and taxonomic revision of Lopadostoma. Persoonia 32:52–82

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jaklitsch WM, Gardiennet A, Voglmayr H (2016) Resolution of morphology-based taxonomic delusions: Acrocordiella, Basiseptospora, Blogiascospora, Clypeosphaeria, Hymenopleella, Lepteutypa, Pseudapiospora, Requienella, Seiridium and Strickeria. Persoonia 37:82–105

    Google Scholar 

  • Jaklitsch WM, Voglmayr H (2012) Phylogenetic relationships of five genera of Xylariales and Rosasphaeria gen. nov. (Hypocreales). Fungal Divers 52:75–98

    Article  Google Scholar 

  • Jaklitsch WM, Voglmayr H (2014) Persistent hamathecial threads in the Nectriaceae, Hypocreales: Thyronectria revisited and re-instated. Persoonia 33:182–211

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Jayasiri SC, Hyde KD, Ariyawansa HA, Bhat DJ, Buyck B, Cai L, Dai YC, Abd-Elsalam KA, Ertz D, Hidayat I, Jeewon R, Jones EBG, Bahkali AH, Karunarathna SC, Liu JK, Luangsa-ard JJ, Lumbsch HT, Maharachchikumbura SSN, McKenzie EHC, Moncalvo JM, Ghobad-Nejhad M, Nilsson H, Pang KL, Pereira OL, Phillips AJL, Raspé O, Rollins AW, Romero AI, Etayo J, Selçuk F, Stephenson SL, Suetrong S, Taylor JE, Tsui CKM, Vizzini A, Abdel-Wahab MA, Wen TC, Boonmee S, Dai DQ, Daranagama DA, Dissanayake AJ, Ekanayaka AH, Fryar SC, Hongsanan S, Jayawardena RS, Li WJ, Perera RH, Phookamsak R, Silva NI, Thambugala KM, Tian Q, Wijayawardene NN, Zhao RL, Zhao Q, Kang JC, Promputtha I (2015) The faces of fungi database: fungal names linked with morphology, phylogeny and human impacts. Fungal Divers 74:3–18

    Article  Google Scholar 

  • Jeewon R (2001) Pestalotiopsis taxonomy: molecular phylogenetics, species nomenclature and teleomorph relationships (Doctoral dissertation, The University of Hong Kong (Pokfulam, Hong Kong)

  • Jeffries P, Young TWK (1994) Interfungal Parasitic Relationships. CAB International, Wallingford

    Google Scholar 

  • Johnson D, Sung GH, Hywel-Jones NL, Luangsa-ard JJ, Bischoff JF, Kepler RM, Spatafora JW (2009) Systematics and evolution of the genus Torrubiella (Hypocreales, Ascomycota). Mycol Res 113:279–289

    Article  CAS  PubMed  Google Scholar 

  • Johnson TW, Sparrow FK (1961) Fungi in Oceans and Estuaries. XXII u. 668 S., 7 Abb., 19 Tab., 17 Taf., Weinheim J. Cramer. Preis DM

  • Joly P (1961) Le genre Sphaerodothis Shear. Bull Res Counc Isr 10D:187–193

    Google Scholar 

  • Jones EBG (1995) Ultrastructure and taxonomy of the aquatic ascomycetous order Halosphaeriales. Can J Bot 73:790–801

    Article  Google Scholar 

  • Jones EBG, Chatmala I, Klaysuban A, Pang KL (2008) Ribosomal DNA phylogeny of marine anamorphic fungi: Cumulospora varia, Dendryphiella species and Orbimyces spectabilis. Raffles Bull Zool Suppl 19:11–18

    Google Scholar 

  • Jones EBG, Eaton RA (1969) Savoryella lignicola gen. et sp. nov. from water cooling towers. Trans Br Mycol Soc 52:161–174

    Article  Google Scholar 

  • Jones EBG, Hyde KD (1992) Taxonomic studies on Savoryella Jones et Eaton (Ascomycotina). Bot Mar 35:83–91

    Google Scholar 

  • Jones EBG, Hyde KD, Read SJ, Moss ST, Alias SA (1996) Tirisporella gen. nov., an ascomycete from the mangrove palm Nypa fruticans. Can J Bot 74:1487–1495

    Article  Google Scholar 

  • Jones EBG, Johnson RG, Moss ST (1983) Taxonomic studies of the Halosphaeriaceae: Corollospora Werdermann. Bot J Linn Soc 87:193–212

    Article  Google Scholar 

  • Jones EBG, Johnson RG, Moss ST (1984) Taxonomic studies of the Halosphaeriaceae: Halosphaeria Linder. Bot Mar 27:129–143

    Article  Google Scholar 

  • Jones EBG, Moss ST (1978) Ascospore appendages of marine ascomycetes: an evaluation of appendages as taxonomic criteria. Mar Biol 49:11–26

    Article  Google Scholar 

  • Jones EBG, Sakayaroj J, Suetrong S, Somrithipol S, Pang KL (2009a) Classification of marine Ascomycota, anamorphic taxa and Basidiomycota. Fungal Divers 35:1–187

    Google Scholar 

  • Jones EBG, Suetrong S, Cheng WH, Rungjindamai N, Sakayaroj J, Boonyuen N, Somrothipol S, Abdelwahab MA, Pang KL (2014) An additional fungal lineage in the Hypocreomycetidae (Falcocladium species) and the taxonomic revaluation of Chaetosphaeria chaetosa and Swampomyces species, based on morphology, ecology and phylogeny. Cryptogam Mycol 35:119–138

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Jones EBG, Zuccaro A, Mitchell J, Nakagiri A, Chatmala I, Pang KL (2009b) Phylogenetic position of freshwater and marine Sigmoidea species: introducing a marine hyphomycete Halosigmoidea gen. nov. (Halosphaeriales). Bot Mar 52(4):349–359

    Article  CAS  Google Scholar 

  • Jones KG, Blackwell M (1998) Phylogenetic analysis of ambrosia species in the genus Raffaelea based on 18S rDNA sequences. Mycol Res 102:661–665

    Article  CAS  Google Scholar 

  • Jong S, Davis E (1976) Contribution to the knowledge of Stachybotrys and Memnoniella in culture. Mycotaxon 3:409–485

    Google Scholar 

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

    Google Scholar 

  • Ju YM, San Martín F, Rogers JD (1993) Three xylariaceous fungi with scolecosporous conidia. Mycotaxon 47:219–228

    Google Scholar 

  • Justavino DR, Kirschner R, Piepenbring M (2015) New species and new records of Meliolaceae from Panama. Fungal Divers 70:73–84

    Article  Google Scholar 

  • Kaewchai S, Soytong K, Hyde KD (2009) Mycofungicides and fungal biofertilizers. Fungal Divers 38:25–50

    Google Scholar 

  • Kang JC, Hyde KD, Kong RYC (1999a) Studies on Amphisphaeriales: The Amphisphaeriaceae (sensu stricto). Mycol Res 103:53–64

    Article  Google Scholar 

  • Kang JC, Hyde KD, Kong RYC (1999b) Studies on the Amphisphaeriales. The genera excluded from the Amphisphaeriaceae, Cainiaceae and Clypeosphaeriaceae. Fungal Divers 2:135–151

    Google Scholar 

  • Kang JC, Hyde KD, Kong RYC (1999c) Studies on Amphisphaeriales l: the Clypeosphaeriaceae. Mycoscience 40:151–164

    Article  Google Scholar 

  • Kang JC, Kong RYC, Hyde KD (1998) Studies on the Amphisphaeriales I. Amphisphaeriaceae (sensu stricto) and its phylogenetic relationships inferred from 5.8 S rDNA and ITS2 sequences. Fungal Divers 1:147–157

    Google Scholar 

  • Kang JC, Kong RYC, Hyde KD (2002) Phylogeny of Amhisphaeriaceae (sensu stricto) and related taxa revisited based on nrDNA sequences. Mycotaxon 81:321–330

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

    Google Scholar 

  • Keim J, Mishra B, Sharma R, Ploch S, Thines M (2014) Root-associated fungi of Arabidopsis thaliana and Microthlaspi perfoliatum. Fungal Divers 66:99–111

    Article  Google Scholar 

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

    Article  PubMed  Google Scholar 

  • Kepler RM, Sung G-H, 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 

  • Khan Z, Gené J, Ahmad S, Cano J, Al-Sweih N, Joseph L, Guarro J (2013) Coniochaeta polymorpha, a new species from endotracheal aspirate of a preterm neonate, and transfer of Lecythophora species to Coniochaeta. Antonie Van Leeuwenhoek 104:243–252

    Article  CAS  PubMed  Google Scholar 

  • Kirk PM (1985) New or interesting microfungi. XIV. Dematiaceous hyphomycetes from Mt Kenya. Mycotaxon 23:305–352

    Google Scholar 

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

    Google Scholar 

  • Kirk PM, Cannon PF, Minter DW, Stalpers JA (2008) Dictionary of the fungi, 10th edn. CABI, Wallingford

    Google Scholar 

  • Kirschstein W (1936) Albertiniella Kirschst. Ann Mycol 34:183

    Google Scholar 

  • Kirschstein W (1939) Über neue, seltene und kritische Ascomyceten und Fungi Imperfecti. II. Ann Mycologici 37:88–140

  • Klaubauf S, Tharreau D, Fournier E, Groenewald JZ, Crous PW, de Vries RP, Lebrun MH (2014) Resolving the polyphyletic nature of Pyricularia (Pyriculariaceae). Stud Mycol 79:85–120

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Klaysuban A, Sakayaroj J, Jones EBG (2014) An additional marine fungal lineage in the Diatrypaceae, Xylariales: Pedumispora rhizophorae. Bot Mar 57:413–420

    Article  Google Scholar 

  • Klebahn H (1929) Vergilbende junge Treibgurken, ein darauf gefundenes Cephalosporium und dessen Schlauchfrüchte. Phytopathol Z 1:31–44

    Google Scholar 

  • Kobayashi T (1970) Taxonomic studies of japanese diaporthaceae with special reference to their life-histories. Forest Pathology Unit, Forest Pathology Section, Government Forest Experiment Station, Shimomeguro 5, Meguro, Tokyo, Japan

  • Kobayasi Y (1941) The genus Cordyceps and its allies. Sci Rep Tokyo Bunrika Daigaku 5:53–260

    Google Scholar 

  • Koch J, Pang KL, Jones EBG (2007) Rostrupiella danica gen. et sp. nov., a Lulworthia-like marine lignicolous species from Denmark. Bot Mar 50:294–301

    Article  CAS  Google Scholar 

  • Koch J, Jones EBG (1984) Lulworthia lignoarenaria, a new marine pyrenomycete from coastal sands. Mycotaxon 20:389–395

    Google Scholar 

  • Kohlmeyer J (1972) A revision of Halosphaeriaceae. Can J Bot 50:1951–1963

    Article  Google Scholar 

  • Kohlmeyer J (1973) Spathulosporales, a new order and possible missing link between Laboulbenniales and Pyrenomycetes. Mycologia 65:614–647

    Article  Google Scholar 

  • Kohlmeyer J (1975) Revision of algicolous Zignoëlla spp. and description of Pontogeneia gen. nov. (Ascomycetes). Bot Jahrb Syst Pflanzengesch Pflanzengeogr 96:200–211

    Google Scholar 

  • Kohlmeyer J (1986) Taxonomic studies of the marine Ascomycotina. In: Moss ST (ed) The biology of marine fungi. Cambridge Univ Press, Cambridge, pp 234–257

    Google Scholar 

  • Kohlmeyer J, Demoulin V (1981) Parastic and symbiotic fungi on marine algae. Bot Mar 24:9–18

    Article  Google Scholar 

  • Kohlmeyer J, Kohlmeyer E (1979) Marine Mycology. The Higher Fungi. Academic, New York

    Google Scholar 

  • Kohlmeyer J, Spatafora JW, Volkmann-Kohlmeyer B (2000) Lulworthiales, a new order of marine Ascomycota. Mycologia 92:453–458

    Article  Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B (1987) Koralionastaceae fam. nov. (Ascomycetes) from coral rock. Mycologia 79:764–778

    Article  Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B (1989) Hawaiian marine fungi, including two new genera of Ascomycotina. Mycol Res 92:410–421

    Article  Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B (1990) New species of Koralionastes (Ascomycotina) from the Caribbean and Australia. Can J Bot 68:1554–1559

    Article  Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B (1993) Two new genera of Ascomycotina from salt marsh Juncus. Syst Ascomycetum 11:95–103

    Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B, Eriksso OE (1997) Fungi on Juncus roemerianus. New obligate and facultative marin ascomycotina. Bot Mar 40:291–300

    Google Scholar 

  • Kohlmeyer J, Volkmann-Kohlmeyer B, Eriksson OE (1995) Fungi on Juncus roemerianus. 2. New dictyosporous ascomycetes. Bot Mar 38:165–174

    Google Scholar 

  • Kolařík M, Hulcr J (2008) Mycobiota associated with the ambrosia beetle Scolytodesunipunctatus (Coleoptera: Curculionidae, Scolytinae). Mycol Res 113:44–60

    Article  PubMed  Google Scholar 

  • Krause RA, Webster RK (1972) The morphology, taxonomy and sexuality of the rice stem rot fungus, Magnaporthe salvinii (Leptosphaeria salvinii). Mycologia 64:103–114

    Article  Google Scholar 

  • Kreisel H (1969) Grunzüge eines natürlichen Systems der Pilze 1–245

  • Krug JC (1977) The genus Cainia and a new family, Cainiaceae. Sydowia 30:122–133

    Google Scholar 

  • Kruys Å, Huhndorf SM, Miller AN (2014) Coprophilous contributions to the phylogeny of Lasiosphaeriaceae and allied taxa within Sordariales (Ascomycota, Fungi). Fungal Divers 70:101–113

    Article  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 64:181–203

    Article  Google Scholar 

  • Kumar S, Stecher G, Peterson D, Tamura K (2012) MEGA-CC: computing core of molecular evolutionary genetics analysis program for automated and iterative data analysis. Appl Note 28:2685–2686

    Article  CAS  Google Scholar 

  • Kuntze O (1891) Rivisio genera plantarum. 2:849–850

  • Lackner M, Hagen F, Meis JF, Gerrits van den Ende AH, Vu D, Robert V, Fritz J, Moussa AA, de Hoog GS (2014) Susceptibility and diversity in therapy-refractory genus Scedosporium. Antimicrob Agents Chemother 58:5877–5885

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lebert H (1858) Ueber einige neue oder unvollkommen gekannte Krankheiten der Insekten, welche durch Entwicklung niederer Pflanzen im lebenden Korper enstehen Zeit. Wiss Zool 9:439–453

  • Læssøe T (1994) Index Ascomycetum I. Xylariaceae. Syst Ascomycetum 13:43–112

    Google Scholar 

  • Laflamme G (1976) Les genres Melogramma Fries et Melanamphora gen. nov., Sphaeriales. Sydowia 28:237–274

    Google Scholar 

  • Lee S, Groenewald JZ, Crous PW (2004) Phylogenetic reassessment of the coelomycete genus Harknessia and its teleomorph Wuestneia (Diaporthales), and the introduction of Apoharknessia gen. nov. Stud Mycol 50:235–252

    Google Scholar 

  • Leuchtmann A, Müller E (1986) Über Thyridium vestitum und sein Anamorph (Ascomycetes). Bot Helv 96:283–287

    Google Scholar 

  • Li H, Xiao J, Gao YQ, Tang JJ, Zhang AL, Gao JM (2014) Chaetoglobosins from Chaetomium globosum, an endophytic fungus in Ginkgo biloba, and their phytotoxic and cytotoxic activities. J Agric Food Chem 62:3734–3741

    Article  CAS  PubMed  Google Scholar 

  • Li Q, Kang JC, Hyde KD (2015a) A multiple gene genealogy reveals the phylogenetic placement of Iodosphaeria tongrenensis sp. nov. in Iodosphaeriaceae (Xylariales). Phytotaxa 234:121–132

    Article  Google Scholar 

  • Li W-J, Maharachchikumbura SSN, Li Q-R, Bhat DJ, Camporesi E, Tian Q, Senanayake IC, Dai D-Q, Chomnunti P, Hyde KD (2015b) Epitypification of Broomella vitalbae and introduction of a novel species of Hyalotiella. Cryptogam Mycol 36:93–108

    Article  Google Scholar 

  • Lindau G (1897) Hypocreales. In: Englier HA, Prantl, KAE (eds) Die Naturlichen Pflanzenfamilien 1(1). Verlag W. Engelman, Leipzig, 343, 372

  • Link HF (1826) Entwurf eines phytologischen Pflanzensystems nebst einer Anordnung der Kryptogamen. AbhKöniglichen Akademie Wiss Berl Dem Jahre 1824:145–194

    Google Scholar 

  • Link HF (1833) Handbuch zur Erkennung der nutzbarsten und am häufigsten vorkommenden Gewächse. Dritter Theil. Berlin: Haude & Spener 1–156

  • Liu D (ed) (2011) Molecular Detection of Human Bacterial Pathogens. Taylor & Francis CRC Press, Boca Raton

    Google Scholar 

  • Liu JK, Hyde KD, Jones EBG, Ariyawansa HA, Bhat DJ, Boonmee S, Maharachchikumbura SSN, McKenzie EHC, Phookamsak R, Phukhamsakda R, Abdel-Wahab MA, Buyck B, Chen J, Chethana KWT, Singtripop C, Dai DQ, Dai YC, Daranagama DA, Dissanayake AJ, Doliom M, Fan LX, Goonasekara ID, Hirayama K, Hongsanan S, Jayasiri SC, Jayawardena RS, Karunarathna SC, Li WJ, Mapook A, Norphanphoun C, Pang KL, Perera RH, Peršoh D, Pinruan U, Senanayake IC, Somrithipol S, Seutrong S, Tanaka K, Thambugala KM, Tian Q, Tibpromma S, Udayanga D, Wijayawardene NN, Wanasinghe D, Abdel-Aziz FA, Adamčík S, Bahkali AH, Boonyuen N, Bulgakov T, Callac P, Chomnunti P, Greiner K, Hashimoto A, Hofstetter V, Kang JC, Li XH, Liu ZY, Matumura M, Mortimer PE, Rambold R, Randrianjohany E, Sato G, Indrasutdhi VS, Verbeken A, 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 

  • Liu F, Hu DM, Cai L (2012) Conlarium duplumascospora gen. et. sp. nov. and Jobellisia guangdongensis sp. nov. from freshwater habitats in China. Mycologia 104:1178–1186

    Article  PubMed  Google Scholar 

  • Liu TT, Hu DM, Cai L, Liu F (2013) Polyphasic characterization of Plectosphaerella oligotrophica, a new oligotrophic species from China. Mycoscience 54:387–393

    Article  CAS  Google Scholar 

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

    Google Scholar 

  • Locquin MV (1972) Synopsis generalis fungorum, excerpta ex libro ‘De Taxia Fungorum’. Revue de Mycologie, Supplémen

  • Locquin-Linard M (1975) Faurelina, nouveau genre d’Ascomycètes (Chadefaudiellaceae?). Rev Mycol 39:125–129

    Google Scholar 

  • Lohde (1874) Bull Res Counc Israel 47: 206 Check (http://www.mycobank.org/Biolomics.aspx?Table=Mycobank&MycoBankNr_=8454)

  • Lombard L, van der Merwe NA, Groenewald JZ, Crous PW (2015) Generic concepts in Nectriaceae. Stud Mycol 80:189–245

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lu BS, Hyde KD (2000) A world monograph of Anthostomella. Fungal Divers Res Series 4:1–376

  • Luangsa-ard J, Houbraken J, van Doorn T, Hong SB, Borman AM, Hywel-Jones NL, Samson RA (2011) Purpureocillium, a new genus for the medically important Paecilomyces lilacinus. FEMS Microbiol Lett 321(2):141–149

  • Lumbsch HT, Huhndorf SM (2007a) Outline of Ascomycota-2007. Myconet 13:1–58

    Google Scholar 

  • Lumbsch HT, Huhndorf SM (2007b) Whatever happened to the pyrenomycetes and loculoascomycetes? Mycol Res 111:1064–1074

    Article  PubMed  Google Scholar 

  • Lumbsch HT, Huhndorf SM (2010) Myconet volume 14 Part One. Outline of Ascomycota-2009. Fieldiana Life Earth Sci 1:1–922

    Article  Google Scholar 

  • Lundqvist N (1972) Nordic Sordariaceae s. lat. Symb Bot Ups 20(1):1–374

    Google Scholar 

  • Luo J, Walsh E, Blystone D, Zhang N (2015) Five new Pseudophialophora species from grass roots in the oligotrophic pine barrens ecosystem. Fungal Biol. doi:10.1016/j.funbio.2015.08.016

    Google Scholar 

  • Luo J, Walsh E, Zhang N (2014) Four new species in Magnaporthaceae from grassroots in New Jersey Pine Barrens. Mycologia 106:580–588

    Article  PubMed  Google Scholar 

  • Luo J, Zhang N (2013) Magnaporthiopsis, a new genus in Magnaporthaceae (Ascomycota). Mycologia 105:1019–1029

    Article  PubMed  Google Scholar 

  • Luttrell ES (1951) Taxonomy of the Pyrenomycetes. Curators Univ Mo 24:1–3

    Google Scholar 

  • Maas JL, Pollack FG, Uecker FA (1979) Morphology and development of Pilidiella quercicola. Mycologia 71:93–102

    Article  Google Scholar 

  • Maharachchikumbura SSN, Guo LD, Chukeatirote E, Bahkali AH, Hyde KD (2011) Pestalotiopsis –morphology, phylogeny, biochemistry and diversity. Fungal Divers 50:167–187

  • Maharachchikumbura SN, Hyde KD, Jones EBG, McKenzie EHC, Huang SK, Abdel-Wahab MA, Daranagama DA, Dayarathne M, D’souza MJ, Goonasekara ID, Hongsanan S, Jayawardena RS, Kirk PM, Konta S, Liu JK, Liu Z-Y, Norphanphoun C, Pang KL, Perera RH, Senanayake IC, Shang Q, 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, Groenewald JZ, Xu J, Crous PW (2014) Pestalotiopsis revisited. Stud Mycol 79:121–186

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mains EB (1950) Entomogenous species of Akanthomyces, Hymenostilbe and Insecticola in North America. Mycologia 42:566–589

    Article  Google Scholar 

  • Mains EB (1951) Entomogenous species of Hirsutella, Tilachlidium and Synnematium. Mycologia 43:691–718

    Article  Google Scholar 

  • Malloch D (1970) New concepts in the Microascaceae illustrated by two new species. Mycologia 62:727–740

  • Malloch D, Cain RF (1970) Five new genera in the new family Pseudeurotiaceae. Can J Bot 48:1815–1825

    Article  Google Scholar 

  • Malloch D, Blackwell M (1990) Kathistes, a new genus of pleomorphic ascomycetes. Can J Bot 68:1712–1721

    Article  Google Scholar 

  • Malloch D, Cain RF (1971) New cleistothecial Sordariaceae and a new family, Coniochaetaceae. Can J Bot 49:869–880

    Article  Google Scholar 

  • Manamgoda DS, Udayanga D, Cai L, Chukeatirote E, Hyde KD (2013) Endophytic Colletotrichum from tropical grasses with a new species C. endophytica. Fungal Divers 61:107–115

    Article  Google Scholar 

  • Marais GJ, Wingfield MJ, Viljoen CD, Wingfield BD (1998) A new ophiostomatoid genus from Protea infructescences. Mycologia 90:136–141

    Article  CAS  Google Scholar 

  • Marincowitz S, Crous PW, Groenewald JZ, Wingfield MJ (2008) Microfungi occurring on Proteaceae in the fynbos. CBS Biodivers Ser 7:1–166

    Google Scholar 

  • Marincowitz S, Gryzenhout M, Wingfield MJ (2010) New and rare coelomycetes with appendage-bearing conidia from Pondoland, South Africa. Mycotaxon 111:309–322

    Article  Google Scholar 

  • Martínez-Rivera K, Heredia G, Rosique-Gil E, Cappello S (2014) Hongos anamorfos asociados a restos vegetales del Parque Estatal “Agua Blanca”, Macuspana, Tabasco, México. Act Bot Mex 107:99–119

    Google Scholar 

  • Massoumi Alamouti S, Kim JJ, Humble L, Uzunovic A, Breuil C (2007) Ophiostomatoid fungi associated with the northern spruce engraverperturbatus, in western Canada. Antonie Van Leeuwenhoek 91:19–34

    Article  CAS  PubMed  Google Scholar 

  • Matsushima T (1987) Matsushima mycological memoir, No. 5. Matsushima, Kobe, Japan

  • Mbenoun M, De Beer ZW, Wingfield MJ, Wingfield BD, Roux J (2014) Reconsidering species boundaries in the Ceratocystis paradoxa complex, including a new species from oil palm and cacao in Cameroon. Mycologia 106:757–784

    Article  PubMed  Google Scholar 

  • McNeill J, Barrie FF, Buck WR, Demoulin V, Greuter W, Hawksworth DL, Herendeen PS, Knapp S, Marhold K, Prado J, Prud’homme van Reine WF, Smith GF, Wiersema J, Turland NJ (eds) (2012) International Code of Nomenclature for algae, fungi and plants (Melbourne Code). Adopted by the 18th International Botanical Congress, Melbourne, Australia, Jul 2011. Regnum Veg, Koeltz Scientific Books, Germany

  • 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 

  • 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 RS, Aneja KR (1990) An introduction to mycology. New Age International

  • Mejía LC, Castlebury LA, Rossman AY, Sogonov MV, White JF (2011) A systematic account of the genus Plagiostoma (Gnomoniaceae, Diaporthales) based on morphology, host-associations, and a four-gene phylogeny. Stud Mycol 68:211–235

    Article  PubMed  PubMed Central  Google Scholar 

  • Mercado-Sierra A, Holubova-Jechova V, Mena Portales J (1997) Monografie XXIII. Hifomycetes demaciaceos de Cuba. Enteroblasticos. Torino, Cuba: Museo Regionale Di Scienze Naturali 352–354

  • Meyers SP (1957) Taxonomy of marine Pyrenomycetes. Mycologia 49:475–528

    Article  Google Scholar 

  • Mibey RK, Hawksworth DL (1997) Meliolaceae and Asterinaceae of the Shimba Hills, Kenya. Mycol Pap 174:1–108

    Google Scholar 

  • Miller AN, Huhndorf SM (2004) A natural classification of Lasiosphaeria based on nuclear LSU rDNA sequences. Mycol Res 108:26–34

    Article  CAS  PubMed  Google Scholar 

  • Miller AN, Huhndorf SM (2005) Multigene phylogenies indicate ascomal wall morphology is a better predictor of phylogenetic relationships than ascospore morphology in the Sordariales (Ascomycota, Fungi). Mol Phylogenet Evol 35:60–75

    Article  CAS  PubMed  Google Scholar 

  • Miller AN, Huhndorf SM (2009) Pyrenomycetes of the World: http://www-s.life.illinois.edu/pyrenos/records/show_by_page?page=53

  • Miller AN, Huhndorf SM, Fournier J (2014) Phylogenetic relationships of five uncommon species of Lasiosphaeria and three new species in the Helminthosphaeriaceae (Sordariomycetes). Mycologia 106:505–524

    Article  PubMed  Google Scholar 

  • Miller JH (1930) British Xylariaceae. Trans Br Mycol Soc 15(1–4):134–154

    Article  Google Scholar 

  • Miller JH (1949) A revision of the classification of the Ascomycetes with special emphasis on the Pyrenomycetes. Mycologia 41:99–127

    Article  Google Scholar 

  • Miranda BE, Barreto RW, Crous PW, Groenewald JZ (2012) Pilidiella tibouchinae sp. nov. associated with foliage blight of Tibouchina granulosa (quaresmeira) in Brazil. IMA Fungus 3(1):1–7

  • Mitchell RS (1937) Stem end rot of bananas with special reference to the physiological relationships of Thielaviopsis paradoxa (De Seyes) von Höhn. J Councilfor Sci Ind Res Aust 10:123–130

    Google Scholar 

  • Montagne C (1834) Description de plusieurs nouvelles espèces de cryptogames découvertes par M. Gauchichaud dans l’Amerique méridional. Ann Sci Nat Bot Ser 2(2):73–79

    Google Scholar 

  • Moreau F (1953) Etude du développement de quelques Aspergillecées. Rev de Mycol 18:165–180

    Google Scholar 

  • Morgan-Jones G, Nag Raj TR, Kendrick WB (1972) Genera coelomycetarum V. Alpakesa and Bartalinia. Can J Bot 50:877–882

    Article  Google Scholar 

  • Morgenstern I, Powlowski J, Ishmael N, Darmond C, Marqueteau S, Moisan MC, Tsang A (2012) A molecular phylogeny of thermophilic fungi. Fungal Biol 116:489–502

    Article  CAS  PubMed  Google Scholar 

  • Morton FJ, Smith G (1963) The genera Scopulariopsis Bainier, Microascus, Zukal and Doratomyces Corda. Mycol Pap 86:1–96

    Google Scholar 

  • Mostert L, Crous PW, Groenewald JZ, Gams W, Summerbell R (2003) Togninia (Calosphaeriales) is confirmed as teleomorph of Phaeoacremonium by means of morphology, sexual compatibility, and DNA phylogeny. Mycologia 95:646–659

    Article  PubMed  Google Scholar 

  • Mostert L, Groenewald JZ, Summerbell RC, Gams W, Crous PW (2006) Taxonomy and pathology of Togninia (Diaporthales) and its Phaeoacremonium anamorphs. Stud Mycol 54:1–115

    Article  Google Scholar 

  • Mouton M, Wingfield MJ, Van Wyk PS, Van Wyk PWJ (1994) Graphiumpseudormiticum sp. nov.: a new hyphomycete with unusual conidiogenesis. Mycol Res 98:1272–1276

    Article  Google Scholar 

  • Mugambi GK, Huhndorf SM (2010) Multigene phylogeny of the Coronophorales: morphology and new species in the order. Mycologia 102:185–210

    Article  CAS  PubMed  Google Scholar 

  • Mühlbauer A, Triebel D, Peršoh D, Wollweber H, Seip S, Stadler M (2002) Macrocarpones, novel metabolites from stromata of Hypoxylon macrocarpum and new evidence on the chemotaxonomy of Hypoxylon. Mycol Prog 1:235–248

    Article  Google Scholar 

  • Mukerji KG (1968) The position of the genus Achaetomium in Pyrenomycetes. Proc Indian Acad Sci, PI Sci 34:288–292

    Google Scholar 

  • Mukerji KG, Manoharachary C (2010) Taxonomy and ecology of Indian fungi. IK International Pvt Ltd 79–80

  • Müller E (1965) Beobachten an Ascomyceten. Sydowia 18:86–105

    Google Scholar 

  • Müller E, Booth C (1972) Generic position of Sphaeria phaeostroma. Trans Br Mycol Soc 58(1):73–77

    Article  Google Scholar 

  • Müller E, Corbaz E (1956) Kulturversuche mit Ascomyceten. III. Sydowia 10:181–188

    Google Scholar 

  • Müller E, Samuels GJ (1982) Anamorphs of pyremycetous Ascomycetes II. Porosphaerella gen. nov. and its Cordana anamorph. Sydowia 35:150–154

    Google Scholar 

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

    Google Scholar 

  • Müller E, von Arx JA (1973) Pyrenomycetes: Meliolales, Coronophorales, Sphaeriales. In: Ainsworth GC, Sparrow FK, Sussman AS (eds) The fungi, vol 6A. Academic, New York, pp 87–132

    Google Scholar 

  • Munk A (1953) The system of Pyrenomycetes. Dansk Bot Arkiv 15:1–163

    Google Scholar 

  • Munk A (1957) Danish Pyrenomycetes. A preliminary flora. Dansk Bot Arkiv 17(1):1–491

    Google Scholar 

  • Murata N, Aoki T, Kusaba M, Tosa Y, Chuma I (2014) Various species of Pyricularia constitute a robust clade distinct from Magnaporthe salvinii and its relativesin Magnaporthaceae. J Gen Plant Pathol 80:66–72

    Article  CAS  Google Scholar 

  • Nag Raj TR (1977) Miscellaneous microfungi. II. Can J Bot 55:757–765

    Article  Google Scholar 

  • Nag Raj TR (1985) Redisposals and redescriptions in the Monochaetia.— Seiridium, Pestalotia—Pestalotiopsis complexes. II. Pestalotiopsis besseyii (Guba) comb. nov. and Pestalosphaeria varia sp. nov. Mycotaxon 22:52–63

    Google Scholar 

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

    Google Scholar 

  • Najwa AM, Sarah AA, Ahmed HFG, Sybren DH, Albertus HGG, Wendy WJ (2012) Pleurostomophora ochracea, a novel agent of human eumycetoma with yellow grains. J Clin Microbiol 50:2987–2994

    Article  CAS  Google Scholar 

  • Nakagiri A (1993) A new marine Ascomycete in Spathulosporales, Hispidicarpomyces galaxauricola gen. et. sp. nov. (Hispidicarpomycetaceae fam. nov.), inhabiting a red alga, Galaxaura falcata. Mycologia 85:638–652

    Article  Google Scholar 

  • Nannfeldt JA (1932) Studien über die Morphologie und Systematikder nicht-lichenisierten, inoperculaten Discomyceten. Nova Acta R Soc Sci Upsaliensis Ser 6(8):1–368

    Google Scholar 

  • Nannfeldt JA (1972) Camarops Karst. (Sphaeriales, Boliniaceae) with special regard to its European species. Sven Bot Tidskr 66:335–376

    Google Scholar 

  • Nannfeldt JA (1975) Stray studies in the Coronophorales (Pyrenomycetes) 4–8. Sven Bot Tidskr 69:289–335

    Google Scholar 

  • Nannizzi A (1934) Repertorio sistematico dei miceti dell’ uomo e degli animali. 4:1–557

  • Nawawi A, Kuthubutheen AJ (1989) Canalisporium, a new genus of lignicolous hyphomycetes from Malaysia. Mycotaxon 34:475–487

    Google Scholar 

  • Nelson NA (1996) Mating systems in ascomycetes: a romp in the sac. Trends Genet 12:69–74

    Article  CAS  PubMed  Google Scholar 

  • Nitschke TH (1867) Pyrenomycetes Germanici., Breslau

    Google Scholar 

  • Okada G, Jacobs K, Kirisits T, Louis-Seize GW, Seifert KA, Sugita T, Takematsu A, Wingfield MJ (2000) Epitypification of Graphium penicillioides Corda, with comments on the phylogeny and taxonomy of graphium-like synnematous fungi. Stud Mycol 45:169–186

    Google Scholar 

  • Okada G, Seifert KA, Takematsu A, Yamaoka Y (1998) A molecular phylogenetic reappraisal of the Graphium complex based on 18S rDNA sequences. Can J Bot 76:1495–1506

    CAS  Google Scholar 

  • Osorio M (1985) Ceratocystis pilifera, HONGO CAUSANTE DE MANCHA AZUL EN MADERA DE Pinus radiata. Bosque (Valdivia) 6(2):116–119

  • Paciura D, Zhou XD, De Beer ZW, Jacobs K, Ye H, Wingfield M (2010) Characterisation of synnematous bark beetle-associated fungi from China, including Graphium carbonarium sp. nov. Fungal Divers 40:75–88

    Article  Google Scholar 

  • Palm ME, Gams W, Nirenberg HI (1995) Plectosporium, a new genus for Fusarium tabacinum, the anamorph of Plectosphaerella cucumerina. Mycologia 87:397–406

    Article  Google Scholar 

  • Pang KL (2002) Systematics of the Halosphaeriales: which morphological characters are important? In: Hyde KD (ed) Fungi in marine environments. Fungal Diversity Press, Hong Kong

    Google Scholar 

  • 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 

  • Parguey-Leduc A (1960) Etude des asques et du développement de l’ Helminthosphaeria clavariarum (Desm.) Fuckel ap. Munk. Bull Soc Mycol Fr 77:15–33

    Google Scholar 

  • Parguey-Leduc A (1977) Les asques des Pyrénomycètes. Revue de Mycologie 41:281–338

    Google Scholar 

  • Parguey-Leduc A, Locquin-Linard M (1976) L’ontogénie et la structures des périthèces de Faurelina fimigenes Locquin-Linard. Rev Mycol 40:161–175

    Google Scholar 

  • Pascoe IG, Nancarrow RJ, Copes CJ (1984) Fusarium tabacinum on tomato and other hosts in Australia. Trans Br Mycol Soc 82:343–345

  • Pazoutova S, Parbery DP (1999) The taxonomy and phylogeny of Claviceps. In: V. I (2en and Cvak L (eds) Ergot. The genus Claviceps. Harwood Academic Publishers, Amsterdam, p 57–77

  • Pearce CA, Hyde KD (1993a) The genus Phyllachora from Australia. P. queenslandica and notes on P. apiculata from Neolitsea. Mycol Res 97:1328–1332

    Article  Google Scholar 

  • Pearce CA, Hyde KD (1993b) The genus Ophiodothella from Australia. Mycol Res 97:1272–1276

    Article  Google Scholar 

  • Pearce CA, Hyde KD (1994) The genus Phyllachora from Australia: observations on taxa from Callistemon species. Mycol Res 98:1393–1401

    Article  Google Scholar 

  • PeiGui L, Doi Y, Xiang Hua W, Qing Bin W (2000) The Hypocreaceae of China III. Some fungicolous species of the genus Hypocrea. Mycosystema 19:317–327

    Google Scholar 

  • Perdomo H, Cano J, Gené J, García D, Hernández M, Guarro J (2013a) Polyphasic analysis of Purpureocilliumlilacinum isolates from different origins and proposal of the new species Purpureocilliumlavendulum. Mycologia 105:151–161

    Article  CAS  PubMed  Google Scholar 

  • Perdomo H, García D, Gené J, Cano J, Sutton DA, Summerbell R, Guarro J (2013b) Phialemoniopsis, a new genus of Sordariomycetes, and new species of Phialemonium and Lecythophora. Mycologia 105:398–421

    Article  PubMed  Google Scholar 

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

    Article  Google Scholar 

  • Petch T (1931b) New species of Cordyceps, collected during the Whitby foray. Nat Hull 1931:101–103

    Google Scholar 

  • Petch T (1932a) Gibellula. Ann Mycol 30:386–393

    Google Scholar 

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

    Article  Google Scholar 

  • Petch T (1938) British Hypocreales. Trans Br Mycol Soc 21:243–305

    Article  Google Scholar 

  • Petrak F (1923) Beiträge zur Pilzflora von Sternberg in Mähren. Ann Mycol 21:107–132

    Google Scholar 

  • Petrak F (1941) Mycologische Notizen. XIV. Ann Mycol 39:251–349

    Google Scholar 

  • Petrak F (1954) Ergebnisse einer Revision der Grundtypen verschiedener Gattungen der Askomyzeten und Fungi imperfecti. V Sydowia 8:287–302

    Google Scholar 

  • Petrini LE, Müller E (1986) Haupt und Nebenfruchtformen europäischer Hypoxylon Arten (Xylariaceae, Sphaeriales) und verwandter Pilze. Mycol Helv 1:501–627

    Google Scholar 

  • Petrini LO, Petrini (1985) Xylariaceous fungi as endophytes. Sydowia 38:216–234

    Google Scholar 

  • Pieckova E (2003) In vitro toxicity of indoor Chaetomium Kunze ex Fr. Ann Agric Environ Med 109–14

  • Pirozynski KA (1974) Xenotypa Petrak and Graphostroma gen. nov., segregates from Diatrypaceae. Can J Bot 52:2129–2135

    Article  Google Scholar 

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

    Article  PubMed  PubMed Central  Google Scholar 

  • Pollack FG, Uecker FA (1974) Monosporascus cannonballus an unusual ascomycete in cantaloupe roots. Mycologia 66:346–349

    Article  Google Scholar 

  • Prados-Rosale RC, Roldán-Rodríguez R, Serena C, López-Berges MS, Josep Guarro J, Martínez-del-Pozo A, Di Pietro A (2012) A PR-1- like protein of Fusarium oxysporum functions in virulence on mammalian host. J Biol Chem 287:21970–21979

    Article  CAS  Google Scholar 

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

    Article  Google Scholar 

  • Preuss CGT (1851) Übersicht untersuchter Pilze, besonders aus der Umgegend von Hoyerswerda. Linnaea 24:99–153

    Google Scholar 

  • Preuss CGT (1852) Übersicht untersuchter Pilze, besonders aus der Umgegend von Hoyerswerda. Linnaea 25:723–742

    Google Scholar 

  • Quandt CA, Kepler RM, Gams W, Araújo JP, Ban S, Evans HC, Hughes D, Humber R, Hywel-Jones N, Li Z, Luangsa-ard JJ, Rehner SA, Sanjuan T, Sato H, Shrestha B, Sung GH, Yao YJ, Zare R, Spatafora JW (2014) Phylogenetic-based nomenclatural proposals for Ophiocordycipitaceae (Hypocreales) with new combinations in Tolypocladium. IMA fungus 5:121–134

    Article  PubMed  PubMed Central  Google Scholar 

  • Quang DN, Hashimoto T, Tanaka M, Baumgartner M, Stadler M, Asakawa Y (2002) Concentricols B, C and D, three novel squalene-type triterpenoids from the ascomycete Daldinia concentrica. Phytochemistry 61:345–353

    Article  CAS  PubMed  Google Scholar 

  • Quang DN, Hashimoto T, Tanaka M, Stadler M, Asakawa Y (2004) Cyclic azaphilones daldinins E and F from the ascomycete fungus Hypoxylon fuscum (Xylariaceae). Phytochemistry 65:469–473

    Article  CAS  PubMed  Google Scholar 

  • Quang DN, Stadler M, Fournier J, Asakawa Y (2006) Carneic acids A and B, two chemotaxonomically significant antimicrobial agents from the xylariaceous ascomycete, Hypoxylon carneum. J Nat Prod 69:1198–1202

    Article  CAS  PubMed  Google Scholar 

  • Raja HA, Campbell J, Shearer CA (2003) Freshwater ascomycetes: Cyanoannulus petersenii, a new genus and species from submerged wood. Mycotaxon 88:1–17

    Google Scholar 

  • Ramaley AW (1997) Barrina, a new genus with polysporous asci. Mycologia 89(6):962–966

    Article  Google Scholar 

  • Randall TA, Metzenberg RL (1995) Species-specific and matingtype-specific DNA regions adjacent to mating-type idiomorphs in the genus Neurospora. Genetics 141:119–136

    CAS  PubMed  PubMed Central  Google Scholar 

  • Ranghoo VM, Hyde KD, Liew ECY, Spatafora JW (1999) Family placement of Ascotaiwania and Ascolacicola based on DNA sequences from the large subunit rRNA gene. Fungal Divers 2:159–168

    Google Scholar 

  • Ranghoo VM, Tsui CKM, Hyde KD (2001) Bruneosporella aquatica gen. et sp. nov., Aqualignicola hyalina gen. et sp. nov., Jobellisia viridifusca sp. nov. and Porosphaerellopsis bipolaris sp. nov. (ascomycetes) from submerged wood in freshwater habitats. Mycol Res 105:625–633

    Article  Google Scholar 

  • Rao V, de Hoog GS (1986) New or critical Hyphomycetes from India. Stud Mycol 28:1–84

    Google Scholar 

  • Rappaz F (1987) Taxonomie et nomenclatijre des Diatrypaceae à asques octospores (1). Mycologia Helvetica 2:285–648

    Google Scholar 

  • Réblová M (1999a) Studies in Chaetosphaeria sensu lato I. The genera Chaetosphaerella and Tengiomyces gen nov of the Helminthosphaeriaceae. Mycotaxon 70:387–420

    Google Scholar 

  • Réblová M (1999b) Studies in Chaetosphaeria sensu lato II. Coniobrevicolla gen & sp nov. Mycotaxon 70:421–429

    Google Scholar 

  • Réblová M (1999c) Studies in Chaetosphaeria sensu lato III. Umbrinosphaeria gen nov and Miyoshiella with Sporidesmium anamorphs. Mycotaxon 71:13–43

    Google Scholar 

  • Réblová M (1999d) Studies in Chaetosphaeria sensu lato IV. Crassochaeta gen. nov., a new lignicolous genus of the Trichosphaeriaceae. Mycotaxon 71:45–67

    Google Scholar 

  • Réblová M (2008) Bellojisia, a new sordariaceous genus for Jobellisia rhynchostoma and a description of Jobellisiaceae fam. nov. Mycologia 100:893–901

    Article  PubMed  CAS  Google Scholar 

  • Réblová M (2013) Two taxonomic novelties in the Sordariomycetidae: Ceratolenta caudata gen. et sp. nov. and Platytrachelon abietis gen. et comb. nov. for Ceratosphaeria abietis. Mycologia 105:462–475

    Article  PubMed  Google Scholar 

  • Réblová M (2014) Sporoschismopsis angustata sp. nov., a new holomorph species in the Retiulascaceae (Glomerellales), and a reappraisal of Sporoschismopsis. Mycol Prog 13:671–681

    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, Fournier J, Hyde KD (2010) Achroceratosphaeria, a new genus for freshwater and terrestrial fungi (Ascomycetes). Fungal Divers 43:75–84

    Article  Google Scholar 

  • Réblová M, Fournier J, Štěpánek V (2015) Pisorisporiales, a new order of aquatic and terrestrial fungi for Achroceratosphaeria and Pisorisporium gen. nov. in the Sordariomycetes. Persoonia 34:40–49

    Article  PubMed  Google Scholar 

  • Réblová M, Gams W (1999) Teleomorph-anamorph connections in Ascomycetes. 1. Cylindrotrichum and Cacumisporium anamorphs of Chaetosphaeria. Czech Mycol 51:1–40

    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

  • Réblová M, Mostert L (2007) Romellia is congeneric with Togninia and description of Conidiotheca gen. nov. for one species of this genus with polysporous asci. Mycol Res 111:299–307

    Article  PubMed  Google Scholar 

  • Réblová M, Mostert L, Gams W, Crous PW (2004) New genera in the Calosphaeriales: Togniniella and its anamorph Phaeocrella, and Calosphaeriophora as anamorph of Calosphaeria. Stud Mycol 50:533–550

    Google Scholar 

  • Réblová M, Seifert KA (2004) Cryptadelphia (Trichosphaeriales), a new genus for holomorphs with Brachysporium anamorphs and clarification of the taxonomic status of Wallrothiella. Mycologia 96:343–367

    Article  PubMed  Google Scholar 

  • Réblová M, Seifert KA (2007) A new fungal genus, Teracosphaeria, with a phialophora-like anamorph (Sordariomycetes, Ascomycota). Mycol Res 3:287–298

    Article  Google Scholar 

  • Réblová M, Seifert KA, Fournier J, Štěpánek V (2016) Newly recognised lineages of perithecial ascomycetes: the new orders Conioscyphales and Pleurotheciales. Persoonia 37:57–81

    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, Winka K (2001) Generic concepts and correlations in ascomycetes based on molecular and morphological data: Lecythothecium duriligni gen. et sp. nov. with a Sporidesmium anamorph, and Ascolacicola austriaca sp. nov. Mycologia 93:479–493

    Article  Google Scholar 

  • Redhead SA, Malloch DW (1977) The Endomycetaceae: new concepts, new taxa. Can J Bot 55:1701–1711

    Article  Google Scholar 

  • Rehm H (1904) Ascomycetes Americae borealis. Ann Myc 2:175–178

    Google Scholar 

  • Rehner SA, Samuels GJ (1994) Taxonomy and phylogeny of Gliocladium analysed from nuclear large subunit ribosomal DNA sequences. Mycol Res 98:625–634

    Article  CAS  Google Scholar 

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

    Article  Google Scholar 

  • Révay Á, Gönczöl J, Descals E (2009) Tulipisopora ingoldii (Hyphomycetes) gen. et sp. nov. from submerged wood. Nova Hedwig 88:41–48

    Article  Google Scholar 

  • Rick JE (1931) Monographia Boliniarum Riograndensium. Brotéria Sér Bot 25:65–71

    Google Scholar 

  • Roane MK, Griffin GJ, Elkins JR (1986) Chestnut blight, other Endothia diseases and the genus Endothia, APS Monograph Series. APS Press, St. Paul, pp 1–53

    Google Scholar 

  • Roets F, Dreyer LL, Wingfield MJ, Crous PW (2013) The taxonomy and ecology of Ophiostomatoid fungi associated with Protea infructescences. In: Seifert KA, de Beer ZW, Wingfield MJ (eds) The ophiostomatoid fungi: expanding frontiers, CBS Fungal Biodivers Ser 12:177–187

  • Rogers DP (1954) The genus Cordyceps and Fries’s observationes. Mycologia 46(2):248–253

  • Rogers JD, Ju YM, San Martín F (1997) Jumillera and Whalleya, new genera segregated from Biscogniauxia. Mycotaxon 64:39–50

    Google Scholar 

  • Rogerson CT (1970) The Hypocrealean Fungi (Ascomycetes, Hypocreales). Mycologia 62:865–910

    Article  CAS  PubMed  Google Scholar 

  • Romero AI, Samuels GJ (1991) Studies on xylophilous fungi from Argentina. VI. Ascomycotina on Eucalyptusviminalis (Myrtaceae). Sydowia 43:228–248

    Google Scholar 

  • Rong IH, Gams W (2000) The hyphomycete genera Exochalara and Monilochaetes. Mycotaxon 76:451–462

    Google Scholar 

  • Rossman AY (2000) Towards monophyletic genera in the holomorphic Hypocreales. Stud Mycol 45:27–34

    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 

  • Rossman AY, Castlebury LA, Samuels GJ (2006) Phylogeny and biodiversity of the Hypocreales and Diaporthales. Eighth International Mycological Congress, Congress Handbook & Abstracts, Book 2:21–25

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

    Article  Google Scholar 

  • Rossman AY, 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, Samuels GJ, Rogerson CT, Lowen R (1999) Genera of Bionectriaceae, Hypocreaceae and Nectriaceae (Hypocreales, Ascomycetes). Stud Mycol 42:3–238

    Google Scholar 

  • Rossman AY, Seifert KA, Samuels GJ, Minnis AM, Schroers HJ, Lombard L, Crous PW, Põldmaa K, Cannon PF, Summerbell RC, Geiser DM, Zhuang W, Hirooka Y, Herrera C, Salgado-Salazar C, Priscila Chaverri P (2013) Genera in Bionectriaceae, Hypocreaceae, and Nectriaceae (Hypocreales) proposed for acceptance or rejection. IMA Fungus 4:41–51

    Article  PubMed  PubMed Central  Google Scholar 

  • Ryley MJ (2003) Nigrocornus scleroticus, a common old world balansioid fungus. In: White JF et al (eds) Clavicipitalean fungi: evolutionary biology, chemistry, biocontrol and cultural impacts. Marcel-Dekker, Inc., New York, pp 247–271

    Google Scholar 

  • Saccardo PA (1873) Fungi Veneti novi vel critici. Series I. Nuovo G Bot Ital 5:269–298

    Google Scholar 

  • Saccardo PA (1877) Fungi Italici autographice delineati a Prof. P.A. Saccardo. Michelia 1(1):73–100

    Google Scholar 

  • Saccardo PA (1878) Fungi Veneti novi vel critici vel mycologiae Venetae addendi. Series VIII. Michelia 1(2):250–251

    Google Scholar 

  • Saccardo PA (1880) Conspectus generum fungorum Italiae inferiorum nempe ad Sphaeropsideas, Melanconieas et Hyphomyceteas pertinentium systemate sporologico dispositorum. Michelia 2(6):1–38

    Google Scholar 

  • Saccardo PA (1882) Sylloge Pyrenomycetum. Sylloge Fungorum 1:1–768

    Google Scholar 

  • Saccardo PA (1883) Pyrenomyceteae. Sylloge Fungorum omnium hucusque cognitorum 2:1–813

    Google Scholar 

  • Saccardo PA (1886) Sylloge Hyphomycetum. Sylloge Fungorum 4:1–807

    Google Scholar 

  • Saccardo PA (1891) Supplementum Universale, Pars I. Agaricaceae-Laboulbeniaceae. Sylloge Fungorum 9:1–1141

    Google Scholar 

  • Saccardo PA (1896) Notes mycologiques (W serie) (I). Bull de la Soc Mycol de Fr 12:64–81

    Google Scholar 

  • Sakayaroj J, Pang KL, Jones EBG, Vrijmoed LLP, Abedl-Wahab MA (2005) A systematic reassessment of marine ascomycetes Swampomyces and Torpedospora. Bot Mar 48:395–406

    Article  Google Scholar 

  • Samson RA, Brady BL (1983) Paraisaria, a new genus for Isariadubia, the anamorph of Cordyceps gracilis. Trans Br Mycol Soc 81:285–290

  • Samson RA, Evans HC (1973) Notes on entomogenous fungi from Ghana. I. The genera Gibellula and Pseudogibellula. Acta Botanica Neerlandica 22:522–528

    Article  Google Scholar 

  • Samson RA, Evans HC (1977) Notes on entomogenous fungi from Ghana. 111. The genus Hymenostilbe. Pt-oc K Ned Akad Wet Ser C 80:128–134

    Google Scholar 

  • Samson RA, Evans HC, Latgé JP (1988) Atlas of entomopathogenic fungi. Springer, Berlin Heidelberg New York

  • Samuels GJ (1988) Fungicolous, lichenicolous, and myxomyceticolous species of Hypocreopsis, Nectriopsis, Nectria, Peristomialis, and Trichonectria. Mem N Y Bot Gard 48:1–78

    Google Scholar 

  • Samuels GJ (1993) The case for distinguishing Ceratocystis and Ophiostoma. In: Wingfield MJ, Seifert KA, Webber JF (eds) Ceratocystis and Ophiostoma. Taxonomy, ecology, and pathogenicity. The American Phytopathological Society Press, St Paul, pp 15–20

    Google Scholar 

  • Samuels GJ, Barr ME (1997) Notes on and additions to the Niessliaceae (Hypocreales). Can J Bot 75:2165–2176

    Article  Google Scholar 

  • Samuels GJ, Blackwell M (2001) Pyrenomycetes—fungi with perithecia. In: McLaughlin DL, McLaughlin EG, Lemke PA (eds) The Mycota—systematics and evolution VII part A. Springer, Verlag, pp 221–255

    Google Scholar 

  • Samuels GJ, Candoussau F, Magni F (1997a) Fungicolous pyrenomycetes 2. Ascocodinaea, gen. nov., and reconsideration of Litschaueria. Mycologia 89:156–162

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Samuels GJ, Müller E, Petrini O (1987) Studies in the Amphisphaeriaceae (sensu lato). 3. New species of Monographella and Pestalosphaeria, and two new genera. Mycotaxon 28:473–499

    Google Scholar 

  • Samuels GJ, Rodrigues KF (1989) Batistia annulipes and its anamorph, Acrostroma annellosynnema. Mycologia 81:52–56

    Article  Google Scholar 

  • Sandoval-Denis M, Gené J, Sutton DA, Cano-Lira JF, de Hoog GS, Decock CA, Wiederhold NP, Guarro J (2016) Redefining Microascus, Scopulariopsis and allied genera. Persoonia 36:1–36

  • Schatz S (1983) The developmental morphology and life history of Phycomelaina laminariae. Mycologia 75:762–772

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

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Schoch CL, Sung GH, Volkmann-Kohlmeyer B, Kohlmeyer J, Spatafora JW (2007) Marine fungal lineages in the Hypocreomycetidae. Mycol Res 111:154–162

    Article  PubMed  Google Scholar 

  • Schroers HJ (2001) A monograph of Bionectria (Ascomycota, Hypocreales Bionectriaceae) and its Clonostachys anamorphs. Stud in Mycol 46:214 Centraalbureau voor Schimmelcultures, Utrecht, The Netherlands

  • Schroers HJ, Gräfenhan T, Seifert KA, Nirenberg H (2011) Fusarium buxicola (Cyanonectria) revised and Geejayessia gen. nov. for Nectria desmazierii and related species with Fusarium-like anamorphs. Stud Mycol 68:115–138

    Article  PubMed  PubMed Central  Google Scholar 

  • Schroeter J (1897) Die Pilze Schlesiens. In: Kryptogamen-Flora von Schlesiens 3(2):385–500

  • Seaver FJ (1909a) The Hypocreales of North America. I. Mycologia 1:41–76

    Article  Google Scholar 

  • Seaver FJ (1909b) The Hypocreales of North America. II. Mycologia 1:177–207

    Article  Google Scholar 

  • Seaver FJ (1910a) The Hypocreales of North America. III. Mycologia 2:48–92

    Article  Google Scholar 

  • Seaver FJ (1910b) Hypocreales. N Amer Flora 3:1–88

    Google Scholar 

  • Seaver FJ (1911) The Hypocreales of North America. IV. Mycologia 3:207–230

    Article  Google Scholar 

  • Seaver FJ (1928a) The North American Cup-Fungi (Operculates) 3:1–284

  • Seaver FJ (1928a) Studies in tropical Ascomycetes-V. Species of Phyllachora. Mycologia 20:214–225

    Article  Google Scholar 

  • Seifert K, Morgan-Jones G, Gams W, Kendrick B (2011) The Genera of Hyphomycetes. [CBS Biodiversity Series 9]. CBS KNAW Fungal Biodiversity Centre, Utrecht

    Google Scholar 

  • Seifert KA (1985) A monograph of Stilbella and some allied hyphomycetes. Stud Mycol 27:1–234

    Google Scholar 

  • Seifert KA (1987) Stromatographium and Acrostroma gen. nov.: two tropical hyphomycete genera with distinctive synnema anatomies. Can J Bot 65:2196–2201

    Article  Google Scholar 

  • Seifert KA (1993) Sapstain of commercial lumber by species of Ophiostoma and Ceratocystis. In: Wingfield MJ, Seifert KA, Webber JF (eds) Ceratocystis and Ophiostoma taxonomy, ecology and pathogenicity. American Phytopathological Society Press, St. Paul, pp 141–151

    Google Scholar 

  • Seifert KA, Okada G (1993) Graphium anamorphs of Ophiostoma species andsimilaranamorphs of other Ascomycetes. In: Wingfield MJ, Seifert KA, Webber J (eds) Ceratocystis and Ophiostoma:taxonomy, ecology andpathogenicity. American Phytopathological Society Press, St. Paul, pp 27–41

    Google Scholar 

  • Semenova EF, Shpichka AI, Moiseeva IY (2012) About essential oils biotechnology on the base of microbial synthesis. Pharm Sci 4:29–31

    Google Scholar 

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

    Article  Google Scholar 

  • Senanayake IC, Maharachchikumbura SSN, Mortimer PE, Bhat JD, Hyde KD (2014) Vialaeaceae; introducing a novel species Vialaea mangiferae. Sydowia 66:203–216

    Google Scholar 

  • Shear CL (1909) Sphaerodothis, a new genus of dothidiaceous fungi. Mycologia 1(4):161–163

    Article  Google Scholar 

  • Shear CL (1923) Life histories and undescribed genera and species of fungi. Mycologia 15:120–131

    Article  Google Scholar 

  • Shear CL (1937) Mycological notes, I. Mycologia 29:355–363

    Article  Google Scholar 

  • Shearer CA, Crane JL, Chen W (1999) Freshwater Ascomycetes: Ophioceras species. Mycologia 91:145–456

    Article  Google Scholar 

  • Shearer CA, Descals E, Kohlmeyer B, Kohlmeyer J, Marvanová L, Padgett D, Porter D, Raja H, Schmit J, Thorton H, Voglymayr H (2007) Fungal biodiversity in aquatic habitats. Biodivers Conserv 16:49–67

    Article  Google Scholar 

  • Shearer CA, Motta JJ (1973) Ultrastructure and conidiogenesis in Conioscypha (Hyphomycetes). Can J Bot 51:1747–1751

    Article  Google Scholar 

  • Shirouzu T, Hirose D, Tokumasu S, To-Anun C, Maekawa N (2010) Host affinity and phylogenetic position of a new anamorphic fungus Beltraniella botryospora from living and fallen leaves of evergreen oaks. Fungal Divers 43:85–92

    Article  Google Scholar 

  • Shoemaker RA, Babcock CE, Müller E (1989) A new Broomella with a Truncatella anamorph on Clematis. Sydowia 41:308–313

    Google Scholar 

  • Shoemaker RA, Hambleton S, Liu M (2013) Vialaea insculpta revisited. N Am Fungi 8(10):1–13

    Google Scholar 

  • Shoemaker RA, Müller E (1963) Generic correlations and concepts: Broomella and Pestalotia. Can J Bot 41:1235–1243

    Article  Google Scholar 

  • Sigler L, Gibas CFC, Kokotovic B, Bertelsen MF (2010) Disseminated mycosis in veiled chameleons (Chamaeleo calyptratus) caused by Chamaeleomyces granulomatis, a new fungus related to Paecilomyces viridis. J Clin Microbiol 48:3182–3192

    Article  PubMed  PubMed Central  Google Scholar 

  • Silvestro D, Michalak I (2011) raxmlGUI: a graphical front-end for RAxML.. doi:10.1007/s13127-011-0056-0, Org Divers Evol

    Google Scholar 

  • Sivanesan A (1976) New British species of Rhamphoria, Trematosphaeria and Chaetosphaerella. Trans Br Mycol Soc 67:469–475

    Article  Google Scholar 

  • Sivanesan A, Alcorn JL (2002) Australiasca queenslandica gen. et sp. nov. (Chaetosphaeriaceae: Ascomycota) and its anamorph Dischloridiumcamelliae sp. nov. from Australia. Aust J Bot 15:741–747

    Article  Google Scholar 

  • Sivanesan A, Shivas RG (2002) New species from each of the pyrenomycete genera Hyponectria, Physalospora and Trichosphaeria from Queensland, Australia. Fungal Divers 9:169–174

    Google Scholar 

  • Skamnioti P, Gurr SJ (2009) Against the grain: safeguarding rice from rice blast disease. Trends Biotechnol 27:141–150

    Article  CAS  PubMed  Google Scholar 

  • Smith GJD, Liew ECY, Hyde KD (2003) The Xylariales: a monophyletic order containing 7 families. Fungal Divers 13:185–218

    Google Scholar 

  • Smyk LV (1981) Griby poriadku Coronophorales u Mikoflory Ukraniy. Ukr Bot Zh 38(6):46–49

    Google Scholar 

  • Sogonov MV, Castlebury LA, Rossman AY, Mejía LC (2008) White JF 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 

  • Somrithipol S, Sudhom N, Tippawan S, Jones EBG (2007) A new species of Falcocladium (Hyphomycetes) with turbinate vesicles from Thailand. Sydowia 59:148–153

    Google Scholar 

  • Sorokin (1888) Zentralblatt für Bakteriologie 4:644

  • Soytong K, Kanokmedhakul S, Kukongviriyapa V, Isobe M (2001) Application of Chaetomium species (Ketomium) as a new broad spectrum biological fungicide for plant disease control. Fungal Divers 7:1–15

    Google Scholar 

  • Spatafora JW, Blackwell M (1993) Molecular systematics of unitunicate perithecial ascomycetes: the Clavicipitales-Hypocreales connection. Mycologia 85:912–922

    Article  CAS  Google Scholar 

  • Spatafora JW, Blackwell M (1994) The polyphyletic origins of ophiostomatoid fungi. Mycol Res 98:1–9

    Article  Google Scholar 

  • Spatafora JW, Johnson D, Sung G-H, Hosaka K, Rourke B, Serdani M, Spotts R, Lutzoni F, Hofstetter V, Fraker E, Gueidan C, Miadlikowska J, Reeb V, Lumbsch T, Lcking R, Schmitt I, Aptroot A, Roux C, Miller A, Geiser D, Hafellner J, Hestmark G, Arnold AE, Bidel B, Rauhut A, Hewitt D, Untereiner W, Cole MS, Scheidegger C, Schultz M, Sipman H, Schoch C (2006) A five-gene phylogenetic analysis of the Pezizomycotina. Mycologia 98:1018–1028

    Article  CAS  PubMed  Google Scholar 

  • Spatafora JW, Quandt CA, Kepler RM, Sung G-H, 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, Volkmann-Kohlmeyer B, Kohlmeyer J (1998) Independent terrestrial origins of the Halosphaeriales (marine Ascomycota). Am J Bot 85:1569–1580

    Article  CAS  PubMed  Google Scholar 

  • Spegazzini C (1919) Fungi Costaricenses nonnulli. Bol Acad Nac Cienc 579:541–609

    Google Scholar 

  • Sri-indrasutdhi V, Boonyuen N, Suetrong S, Chuaseeharonnachai C, Sivichai S, Jones EBG (2010) Wood-inhabiting freshwater fungi from Thailand: Ascothailandia gen. et sp. nov., Canalisporium sp. nov. with a key to Canalisporium species (Sordariomycetes Ascomycota). Mycoscience 51:411–420

    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, Baumgartner M, Grothe T, Mühlbauer A, Seip S, Wollweber H (2001) Concentricol, a taxonomically significant triterpenoid from Daldinia concentrica. Phytochemistry 56:787–793

    Article  CAS  PubMed  Google Scholar 

  • Stadler M, Fournier J, Læssøe T, Chlebicki A, Lechat C, Flessa F, Rambold G, Peršoh D (2010) Chemotaxonomic and phylogenetic studies of Thamnomyces (Xylariaceae). Mycoscience 51:189–207

    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 

  • Stadler M, Læssøe T, Fournier J, Decock C, Schmieschek B, Tichy HV, Peršoh D (2014a) A polyphasic taxonomy of Daldinia (Xylariaceae). Stud Mycol 77:1–143

    Article  PubMed  PubMed Central  Google Scholar 

  • Stadler M, Hawksworth DL, Fournier J (2014b) The application of the name Xylaria hypoxylon, based on Clavaria hypoxylon of Linnaeus. IMA Fungus 5(1):57–66

    Article  PubMed  PubMed Central  Google Scholar 

  • Stchigel AM, Guarro J, Figueras MJ (1996) A new species of Melanospora from India. Mycol Res 101:446–448

    Article  Google Scholar 

  • Steiner U, Leibner S, Schardl CL, Leuchtmann A, Leistner E (2011) Periglandula, a new fungal genus within the Clavicipitaceae and its association with Convolvulaceae. Mycologia 103:1133–1145

    Article  PubMed  Google Scholar 

  • Steyaert RL (1949) Contribution à lnétude monographique de Pestalotia de Not. et Monochaetia Sacc. (Truncatella gen. nov. et Pestalotiopsis gen. nov.). Bull Jard Bot Brux 19(3):285–354

  • 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 DJ, McKenzie EHC, Zhou DQ (2016) The families Distoseptisporaceae fam. nov., Kirschsteiniotheliaceae, Sporormiaceae and Torulaceae, with new species from freshwater in Yunnan Province, China. Fungal Divers. doi:10.1007/s13225-016-0362-0

    Google Scholar 

  • Subileau C, Renard L, Dennetiere B (1993) Phyllachora torrendiella (Batista) comb. nov., responsable de la maladie verruqueuse du cocotier. Mycotaxon 49:175–185

    Google Scholar 

  • Suetrong S, Klaysuban A, Sakayaroj J, Preedanon S, Rung-areerate P, Phongpaichit S, Jones EBG (2015) Tirisporellaceae, a new family in the order Diaporthales (Sordariomycetes, Ascomycota). Crypto Mycol 36:319–330

    Article  Google Scholar 

  • Suh MK, Lim JK, Lee YH, Ha GY, Kim H, Kim JR, Yaguchi T, Nishimura K (2006) Subcutaneous hyalohyphomycosis due to Cephalotheca foveolata in an immunocompetent host. Br J Dermatol 154:1184–1189

    Article  CAS  PubMed  Google Scholar 

  • Suh S, Blackwell M (1999) Molecular phylogeny of the cleistothecial fungi placed in Cephalothecaceae and Pseudeurotiaceae. Mycologia 91:836–848

    Article  CAS  Google Scholar 

  • Summerell BA, Groenewald JZ, Carnegie A, Summerbell RC, Crous PW (2006) Eucalyptus microfungi known from culture. 2. Alysidiella, Fusculina and Phlogicylindrium genera nova, with notes on some other poorly known taxa. Fungal Divers 23:323–350

    Google Scholar 

  • Summerbell RC, Gueidan C, Schroers HJ, De Hoog GS, Starink M, Rosete YA, Guarro J, Scott JA (2011) Acremonium phylogenetic overview and revision of Gliomastix, Sarocladium, and Trichothecium. Stud Mycol 68:139–162

  • Sung GH, Spatafora JW, Zare R, Hodge KT, Gams W (2001) A revision of Verticillium sect. Prostrata. II. Phylogenetic analyses of SSU and LSU nuclear rDNA sequences from anamorphs and teleomorphs of the Clavicipitaceae. Nova Hedwig 72(3–4):311–328

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

    Article  PubMed  PubMed Central  Google Scholar 

  • Sutherland GK (1915) Additional notes on marine pyrenomycetes. Trans Br Mycol Soc 5:257–263

    Article  Google Scholar 

  • Sutton BC (1980) The coelomycetes. Fungi Imperfecti with Pycnidia Acervuli and Stromata. Commonwealth Mycological Insitute, Kew, pp 1–696

    Google Scholar 

  • Sydow H (1924) Sydow, Mycotheca germanica. Fasc. XLII –XLV (No. 2051–2250). Ann Mycol 22:257–268

  • Sydow H, Sydow P (1919) Mykologische mitteilungen. Ann Mycologici 17:33–47

    Google Scholar 

  • Tanaka E, Ashizawa T, Sonoda R, Tanaka C (2008) Villosiclava virens gen. nov., comb. nov., teleomorph of Ustilaginoidea virens, the causal agent of rice false smut. Mycotaxon 106:491–501

    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 

  • Tassi F (1900) Bartalinia Fl. Tassi. Nuovo genere di Sphaeropsidaceae. Boll Laboratorio Bot R Univ Siena 3:3–5

    Google Scholar 

  • Taylor J, Hyde KD (2003) Microfungi of Tropical and Temperate Palms. Fungal Divers Res Ser 12:1–459

    Google Scholar 

  • Teng SC (1934) Fungi of China. In: Korf RP (ed) Mycotaxon Ltd, Ithaca, New York: 151–153

  • Theissen F (1910) Fungi riograndenses. Beih Bot Zentralb 27:384–411

    Google Scholar 

  • Theissen F (1999) Xylariaceae austro-brasilienses. II. Ann Mycol 7(1–18):140–167

    Google Scholar 

  • Theissen F, Sydow H (1915) Die Dothideales. Ann Mycol 13:147–746

    Google Scholar 

  • Thongkantha S, Jeewon R, Vijaykrishna D, Lumyong S, McKenzie EHC, Hyde KD (2009) Molecular phylogeny of Magnaporthaceae (Sordariomycetes) with a new species Ophioceras chiangdaoense from Dracaena loureiroi in Thailand. Fungal Divers 34:157–173

    Google Scholar 

  • Traverso JB (1906) Flora italica cryptogama Pars I: Fungi Pyrenomycetae Fasc 1:1–352

  • 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 

  • Trouillas FP, Sosnowski MR, Gubler WD (2010) Two new species of Diatrypaceae from coastal wattle in Coorong National Park, South Australia. Mycosphere 1:183–188

    Google Scholar 

  • Tsui CKM, Hyde KD (2003) Freshwater mycology. Fungal Divers Res Ser 10:1–350

    Google Scholar 

  • Tsui CKM, Hyde KD, Hodgkiss IJ (1998) A new species of Clohiesia from Hong Kong. Mycoscience 39:257–259

    Article  Google Scholar 

  • Tsui CKM, Leung YM, Hyde KD, Hodgkiss IJ (2001) Three new Ophioceras species (Ascomycetes) from tropics. Mycoscience 42:321–326

    Article  Google Scholar 

  • Tulasne L, Tulasne C (1863b) Selecta fungorum Carpologia. II. (English translation of W. B. Grove). Oxford University Press

  • Tulasne LR (1853) Mémoire sur l’ergot des Glumacées. Ann Scie Nat Bot 20:5–56

    Google Scholar 

  • Tulasne LR, Tulasne C (1861) Selecta Fungorum Carpologia: Erysiphei 1:1–180

  • Tulasne LR, Tulasne C (1863a) Selecta Fungorum Carpologia: Xylariei- Valsei- Spaeriei. 2

  • Udagawa SI, Furuya K (1973) The genus Leuconeurospora. J Jpn Bot 48:111–116

    Google Scholar 

  • Udayanga D, Castlebury LA, Rossman AY, Chukeatirote E, Hyde KD (2014) Insights into the genus Diaporthe: phylogenetic species delimitation in the D. eres species complex. Fungal Divers 67:203–229

    Article  Google Scholar 

  • Udayanga D, Liu XZ, Crous PW, McKenzie EHC, Chukeatirote E, Hyde KD (2012a) A multi-locus phylogenetic evaluation of Diaporthe (Phomopsis). Fungal Divers 56:157–171

    Article  Google Scholar 

  • Udayanga D, Liua X, McKenzie EHC, Chukeatirote E, Hyde KD (2012b) Multilocus phylogeny of Diaporthe reveals three new cryptic species from Thailand. Cryptogam Mycol 33:295–309

    Article  Google Scholar 

  • Uecker FA (1976) Development and cytology of Sordaria humana. Mycologia 68:30–46

    Article  Google Scholar 

  • Uecker FA (1993) Development and cytology of Plectosphaerella cucumerina. Mycologia 85:470–479

    Article  Google Scholar 

  • Uecker FA (1994) On the ontogeny of the ascoma of Glomerella cingulata. Mycologia 86:82–88

    Article  Google Scholar 

  • Untereiner WA, Bogale M, Carter A, Hanson SÅ, Læssøe T, Štěpánek V, Réblová M (2013) Molecular phylogeny of Boliniales (Sordariomycetes) with an assessment of the systematics of Apiorhynchostoma, Endoxyla and Pseudovalsaria. Mycologia 105:564–588

    Article  PubMed  Google Scholar 

  • Upadhyay HP (1981) A Monograph of Ceratocystis and Ceratocystiopsis. Univ. of Georgia Press, Athens, pp 1–176

    Google Scholar 

  • Van Niekerk JM, Groenewald EJZ, Verkley GJM, Fourie PH, Wingfield MJ, Crous PW (2004) Systematic reappraisal of Coniella and Pilidiella, with specific reference to species occurring on Eucalyptus and Vitis in South Africa. Mycol Res 108:283–303

    Article  PubMed  Google Scholar 

  • Varghese KIM, Rao VG (1979) Two new additions to the Indian Ascomycetes. Biovigyanam 5:1–4

    Google Scholar 

  • Vasilyeva LN, Chernyshev AV, Stephenson SL (2012) Neochaetosphaerella thaxteriospora gen. et sp. nov. and Tympanopsis texensis sp. nov. (Coronophorales, Ascomycota) from Texas, USA. Fungal Divers 52:191–196

  • Vasilyeva LN, Chernyshev AV, Stevenson SL, Hyde KD (2013) Tortulomyces thailandicus gen. et sp. nov. and Nitschkia siamensis sp. nov. (Coronophorales, Ascomycota) from northern Thailand. Mycoscience 54(2):110–115

  • Vijaykrishna D, Jeewon R, Hyde KD (2005) Fusoidispora aquatica: a new freshwater ascomycete from Hong Kong based on morphology and phylogeny inferred from rDNA gene sequences. Sydowia 57:267–280

    Google Scholar 

  • Vijaykrishna D, Jeewon R, Hyde KD (2006) Molecular taxonomy, origins and evolution of freshwater ascomycetes. Fungal Divers 23:351–390

    Google Scholar 

  • Vijaykrishna D, Mostert L, Jeewon R, Gams W, Hyde KD, Crous PW (2004) Pleurostomophora, an anamorph of Pleurostoma (Calosphaeriales), a new anamorph genus morphologically similar to Phialophora. Stud Mycol 50:387–395

    Google Scholar 

  • Viljoen CD, Wingfield BD, Wingfield MJ (1999) Relatedness of Custingophora olivacea to Gondwanamyces spp. from Protea spp. Mycol Res 103:497–500

    Article  Google Scholar 

  • Visser AA, Ros VID, de Beer ZW, Debets AJM, Hartog E, Kuyper TW, Laessoe T, Slippers B, Aanen DK (2009) Levels of specificity of Xylaria species associated with fungus-growing termites: a phylogenetic approach. Mol Ecol 18:553–567

    Article  CAS  PubMed  Google Scholar 

  • Voglmayr H, Jaklitsch WM (2008) Prosthecium species with Stegonsporium anamorphs on Acer. Mycol Res 112:885–905

    Article  PubMed  Google Scholar 

  • Voglmayr H, Jaklitsch WM (2014) Stilbosporaceae resurrected: generic reclassification and speciation. Persoonia 33:61–82

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • von Arx JA (1978) Notes on Microascaceae with the description of two new species. Persoonia 10:23–31

    Google Scholar 

  • von Arx JA (1981) The genera of fungi sporulating in pure culture, 3rd edn. Stechert-Hafner, New York, p 288

    Google Scholar 

  • von Arx JA, Müller E (1955) Über die Gattungen Delitschia Auersw., Trichodelitschia Munk, und Cainia nov. gen. Acta Bot Neerl 4:108–115

    Article  Google Scholar 

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

    Google Scholar 

  • von Arx JA, Guarro J, Figueras MJ (1986) The ascomycete genus Chaetomium. J. Cramer

  • von Höhnel F (1907) Fragmente zur Mykologie: IV. Mitteilung (Nr. 156 bis 168). Sitzungsberichte der Kaiserlichen Akademie der Wissenschaften Math.-naturw. Klasse Abt I 116:615–647

    Google Scholar 

  • von Höhnel F (1909) Sitzungsberichte der Kaiserlichen Akademie der Wissenschaften in Wien Mathematisch-Naturwissenschaftliche Classe, Abt. 1, 118: 1513

  • von Höhnel F (1915) Fragmente zur Mykologie (XVII. Mitteilung, Nr. 876 bis 943). Sitzungsberichte der Kaiserlichen Akademie der Wissenschaften Math.-naturw. Klasse Abt I 124:49–159

    Google Scholar 

  • von Höhnel F (1917) Cephalothecaceae. Ann Mycol 15(5):362

    Google Scholar 

  • von Höhnel F (1918) Mycologische Fragmente CCLXII. Ann Mycol 16:127–132

    Google Scholar 

  • Wanderlei-Silva D, Neto ER, Hanlin R (2003) Molecular systematics of the Phyllachorales (Ascomycota, Fungi) based on 18S ribosomal DNA sequences. Braz Arch Biol Technol 46:315–322

    Article  CAS  Google Scholar 

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

    Article  Google Scholar 

  • Wang Y, Xu L, Ren W, Zhao D, Zhu Y, Wu X (2012) Bioactive metabolites from Chaetomium globosum L18, an endophytic fungus in the medicinal plant Curcuma wenyujin. Phytomedicine 19:364–368

    Article  CAS  PubMed  Google Scholar 

  • Wang YZ, Aptroot A, Hyde KD (2004) Revision of the genus Amphisphaeria. Hong Kong SAR, China. Fungal Divers Res Ser 13:1–168

    Google Scholar 

  • Watson W (1929) The classification of lichens. II. New Phytol 28:85–116

    Article  Google Scholar 

  • Webber JF, Gibbs JN (1989) Insect dissemination of fungal pathogens of trees. In: Wilding N, Collins NM, Hammond PM, Webber JF (eds) Proceedings of the 14th Symposium of the Royal Entomological Society of London / British Mycological Society “Insect-Fungus Interactions”. Academic, London, pp 541–546

    Google Scholar 

  • Weber E, Görke C, Begerow D (2002) The Lecythophora-Coniochaeta complex: II. Molecular studies based on sequences of the large subunit of ribosomal DNA. Nova Hedwig 74:187–200

    Article  Google Scholar 

  • Wehmeyer LE (1933) The British species of the genus Diaporthe Nits. and its segregates. Trans Br Mycol Soc 17:237–295

    Article  Google Scholar 

  • Wehmeyer LE (1975) The pyrenomycetous fungi. Mycol Mem 6:1–250

    Google Scholar 

  • Wehmeyer LE (1976) Cataloging the school media center as a specialized collection. li- brary resources. Tech Serv 20:315–325

    Google Scholar 

  • Whalley AJS, Edwards RL (1995) Secondary metabolites and systematic arrangement within the Xylariaceae. Can J Bot 73:802–810

    Article  Google Scholar 

  • White JF Jr, Sullivan MM, Patel R, Duncan R (2000) An overview of problems in the classification of plant-parasitic Clavicipitaceae. Stud Mycol 45:95–105

    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, Wanasinghe DN, Papizadeh M, Goonasekara ID, Camporesi E, Bhat JD, McKenzie EHC, Phillips AJL, Diederich P, Tanaka K, Li WJ, Tangthirasunun N, Phookamsak R, Dai D-Q, Dissanayake AJ, Weerakoon G, Maharachchikumbura SSN, Hashimoto A, Matsumura M, Wang Y (2016) Taxonomy and phylogeny of dematiaceous coelomycetes. Fungal Divers (In press)

  • Wingfield MJ, De Beer C, Visser C, Wingfield BD (1996) A new Ceratocystis species defined using morphological and ribosomal DNA sequence comparisons. Syst Appl Microbiol 19:191–202

    Article  Google Scholar 

  • Wingfield MJ, van Wyk PS (1993) A new species of Ophiostoma from Protea infructescences in South Africa. Mycol Res 97:709–716

    Article  Google Scholar 

  • Wingfield MJ, van Wyk PS, Marasas WFO (1988) Ceratocystiopsis proteae sp. nov., with a new anamorph genus. Mycologia 80:23–30

    Article  Google Scholar 

  • Winka K, Eriksson OE (2000) Papulosa amerospora accommodated in a new family (Papulosaceae, Sordariomycetes, Ascomycota) inferred from morphological and molecular data. Mycoscience 41:96–104

    Article  Google Scholar 

  • Winter G (1885) Pilze: Ascomyceten. In: Rabenhorst’s Kryptogamen-Flora von Deutschland, Oesterreich und der Schweiz 1:1–928

  • Winter G (1887) Pilze, Ascomyceten. In: Rabenhorst’s Kryptogamen Flora von Deutschland, Oesterreich und der Schweiz [i–vi] 1:1–928

  • Wong MKM, Jones EBG, Abdel-Wahab MA, Au DWT, Vrijmoed LLP (2003) Ultrastructure of conidiogenesis and appendage ontogeny in the coelomycete Bartalinia robillardoides. Can J Bot 81:1083–1090

    Article  Google Scholar 

  • Wong SW, Hyde KD, Jones EBG (1998) Annulatascaceae, a new ascomycete family from the tropics. Syst Ascomycetum 16:17–25

    Google Scholar 

  • Wong SW, Hyde KD, Jones EBG (1999) Ultrastructural studies of freshwater ascomycetes Fluminicola bipolaris gen. et sp. nov. Fungal Divers 2:189–197

    Google Scholar 

  • Worapong J, Strobel G, Ford EJ, Li JY, Baird G, Hess WM (2001) Muscodor albus anam. gen. et sp nov., an endophyte from Cinnamomum zeylanicum. Mycotaxon 79:67–79

    Google Scholar 

  • Wraight SP, Carruthers RI, Bradley CA, Jaronski ST, Lacey LA, Wood P, Galaini-Wraight S (1998) Pathogenicity of the entomopathogenic fungi Paecilomyces spp. and Beauveria bassiana against the silver leaf whitefly, Bemisia argentifolii. J Invertebr Pathol 71:217–226

    Article  CAS  PubMed  Google Scholar 

  • Xi PG, Chi PK, Jiang ZD (2000) Three new species of coelomycetes. Mycosystema 19:466–469

    Google Scholar 

  • Xu J, Yang X, Lin Q (2014) Chemistry and biology of Pestalotiopsis derived natural products. Fungal Divers 66:37–68

    Article  Google Scholar 

  • Yaguchi T, Sano A, Yarita K, Suh MK, Nishimura K, Udagawa S (2006) New species of Cephalotheca isolated from a Korean patient. Mycotaxon 96:309–322

    Google Scholar 

  • Yang J, Maharachchikumburaa SSN, Hyde KD, Bhat DJ, Mckenzie EHC, Bahkali AH, Jones EBG, Liu ZY (2015) Aquapteridospora lignicola gen. et sp. nov., a new hyphomycetous taxon (Sordariomycetes) from wood submerged in a freshwater stream. Cryptogam Mycol 36:469–478

    Article  Google Scholar 

  • Yang YL, Cai L, Yu ZN, Liu ZY, Hyde KD (2011) Colletotrichum species on Orchidaceae in southwest China. Cryptogam Mycol 32:229–253

  • Yokoyama E, Arakawa M, Yamagishi K, Hara A (2006) Phylogenetic and structural analyses of the mating-type loci in Clavicipitaceae. FEMS Microbiol Lett 264:182–191

    Article  CAS  PubMed  Google Scholar 

  • Yuan ZQ, Zhao ZY (1992) A new species of Broomella and its new anamorph on Clematis from China. Sydowia 44:90–99

    Google Scholar 

  • Yue JZ, Eriksson OE (1987) Sinosphaeria bambusicola gen. et sp. nov., (Thyridiaceae fam. nov.). Syst Ascomycetum 6:229–236

    Google Scholar 

  • Zare R, Gams W (2001) A revision of Verticillium section Prostrata. VI. The genus Haptocillium. Nova Hedwig 73:271–292

    Google Scholar 

  • Zare R, Gams W, Culham A (2000) A revision of Verticillium sect. Prostrata. I. Phylogenetic studies using ITS sequences. Nova Hedwig 71:465–480

    Google Scholar 

  • Zare R, Gams W, Evans HC (2001) A revision of Verticillium section Prostrata. V. The genus Pochonia, with notes on Rotiferophthora. Nova Hedwig 73:51–58

    Google Scholar 

  • Zare R, Gams W, Starink-Willemse M, Summerbell RC (2007) Gibellulopsis, a suitable genus for Verticillium nigrescens, and Musicillium, a new genus for V. theobromae. Nova Hedwig 85:463–489

    Article  Google Scholar 

  • Zelski SE, Balto JA, Do C, Raja HA, Miller AN, Shearer CA (2014) Phylogeny and morphology of dematiaceous freshwater microfungi from Perú. IMA Fungus 5:425–438

    Article  PubMed  PubMed Central  Google Scholar 

  • Zelski SE, Raja HA, Miller AN, Shearer CA (2011) Chaetorostrum quincemilensis, gen. et sp. nov., a new freshwater ascomycete and its Taeniolella-like anamorph from Peru. Mycosphere 2:593–600

    Article  Google Scholar 

  • Zhang H, Wu Z, Wang C, Li Y, Xu JR (2014) Germination and infectivity of microconidia in the rice blast fungus Magnaporthe oryzae. Nat Comm 5:4518

    CAS  Google Scholar 

  • Zhang N, Blackwell M (2002) Molecular phylogeny of Melanospora and similar pyrenomycetous fungi. Mycol Res 106:148–155

    Article  CAS  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Zhang N, Zhao S, Shen Q (2011) A six-gene phylogeny reveals the evolution of mode of infection in the rice blast fungus and allied species. Mycologia 103:1267–1276

    Article  PubMed  Google Scholar 

  • Zhang Q, Li HQ, Zong SC, Gao JM, Zhang AL (2012a) Chemical and bioactive diversities of the genus Chaetomium secondary metabolites. Mini Rev Med Chem 12:127–148

    Article  PubMed  Google Scholar 

  • Zhang W, Nan Z, Tian P, Hu MJ, Gao ZY, Li M, Liu GD (2015) Microdochium paspali, a new species causing seashore paspalum disease in southern China. Mycologia 107:80–89

    Article  PubMed  Google Scholar 

  • Zhang Y, Maharachchikumbura SSN, McKenzie EHC, Hyde KD (2012b) A novel species of Pestalotiopsis causing leaf spots of Trachycarpus fortunei. Cryptogam Mycol 33:311–318

    Article  Google Scholar 

  • Zhao G, Yu P, Liu X (2012) Cancellidium and Canalisporium (Hyphomycetes) from China. Nova Hedwig 96:221–236

    Article  Google Scholar 

  • Zipfel RD, de Beer ZW, Jacobs K, Wingfield BD, Wingfield MJ (2006) Multi-gene phylogenies define Ceratocystiopsis and Grosmannia distinct from Ophiostoma. Stud Mycol 55:75–97

  • Zukal H (1886) Mykologische Untersuchungen. Demkschriften der Akademie der Wissenschaften (Wien). Math-Naturw 51:21–36

    Google Scholar 

Download references

Acknowledgments

This work was supported by the International Research Group Program (IRG-14-27), Deanship of Scientific Research, King Saud University, Saudi Arabia. The curators of the herbarium ANM, AR, B, BBH, BCC, BISH, BP, BPI, BR, BRIP, CBS, DAOM, FH, G, GZU, GZU, H, HAL, HHUF, HKU (M), IFRD, ILLS, IMI, K, L, LPS, MFU, NY, P, PC, PREM, S, TRTC, UBC, UC, UCR, UPS, URM, URM and W are thanked for loaning herbarium specimens and for being very helpful in locating specimens. Without their help this work would not have been possible. The abbreviations of herbarium are those listed in Index Herbariorum (2015). We also thank the curator of MFLU for arranging the loan of specimens from various herbaria. The authors would like to thank the featured microbial resources and diversity investigation in Southwest Karst area (2014FY120100). This research was also financially supported by The Biodiversity and Training Program (BRT R_251006, BRT R_351004, BRT_R352015) and National Center for Genetic Engineering and Biotechnology (BIOTEC) Khlong Luang, Pathum Thani 12120, Thailand. Shi-Ke Huang’ s work was funded by the grants from the National Natural Science Foundation of China (NSFC, No. 30870009 & 31460011), the International Collaboration Plan of Guizhou Province (No. G [2012] 7006). Ka-Lai Pang thanks the Ministry of Science and Technology, Taiwan (grant no. 101–2621-B-019–001-MY3) for financial support. We are also grateful to Bita Asgari and Rasoul Zare, for images of Coniocessia spp., and Ruvini Nanayakkara, Hiran Ariyawansa, Dhanushka Nadeeshan, Asanka Bandara, Kasun Thambugala, Mingkwan Doilom and Wen-Jing Li for providing assistance and valuable suggestions.

Author information

Authors and Affiliations

  1. Guizhou Key Laboratory of Agricultural Biotechnology, Guizhou Academy of Agricultural Sciences, Guiyang, 550006, Guizhou, China

    Sajeewa S. N. Maharachchikumbura, Rekhani H. Perera, Jian Kui Liu & Zuo-Yi Liu

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

    Sajeewa S. N. Maharachchikumbura, Kevin D. Hyde, Monika C. Dayarathne, Shi-Ke Huang, Chada Norphanphoun, Indunil C. Senanayake, Rekhani H. Perera, Qiu-Ju Shang, Yuanpin Xiao, Melvina J. D’souza, Sinang Hongsanan, Ruvishika S. Jayawardena, Dinushani A. Daranagama, Sirinapa Konta, Ishani D. Goonasekara, Saranyaphat Boonmee, Asha J. Dissanayake, Rungtiwa Phookamsak & Nalin N. Wijayawardene

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

    Sajeewa S. N. Maharachchikumbura & Abdullah M. Al-Sadi

  4. Department of Botany and Microbiology, College of Science, King Saud University, P.O. Box 2455, Riyadh, 11451, Kingdom of Saudi Arabia

    E. B. Gareth Jones, Mohamed A. Abdel-Wahab & Ali H. Bahkali

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

    E. H. C. McKenzie

  6. No. 128/1-J, Azad Housing Society, Curca, P.O. Goa Velha, 403108, Goa, India

    Jayarama D. Bhat

  7. Department of Botany, Goa University, Goa, 403 206, India

    Jayarama D. Bhat

  8. Engineering Research Center of Southwest Bio-Pharmaceutical Resources, Ministry of Education, Guizhou University, Guiyang, 550025, Guizhou Province, China

    Shi-Ke Huang, Yuanpin Xiao, Jichuan Kang, Qi-Rui Li & Tingchi Wen

  9. Institute of Plant and Environment Protection, Beijing Academy of Agriculture and Forestry Sciences, No 9 of ShuGuangHuaYuanZhangLu, Haidian District, Beijing, 100097, China

    Ruvishika S. Jayawardena & Asha J. Dissanayake

  10. State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China

    Dinushani A. Daranagama, Wen-Ying Zhuang & Xing Zhong Liu

  11. Department of Health Sciences, Faculty of Science, University of Mauritius, Reduit, Mauritius

    Rajesh Jeewon

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

    Alan J. L. Phillips

  13. Department of Botany, Faculty of Science, Sohag University, Sohag, Egypt

    Mohamed A. Abdel-Wahab

  14. Fungal Biodiversity Laboratory, BIOTEC, National Science and Technology Development Agency (NSTDA), 113 Thailand Science Park, Thanon Phahonyothin, Tombon Khlong Nueng, Amphoe Khlong Luang, Pathum Thani, 12120, Thailand

    Nattawut Boonyuen & Satinee Suetrong

  15. Department of Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai, 50200, Thailand

    Ratchadawan Cheewangkoon

  16. Department of Pharmacy, Guiyang Medical University, Guiyang, Guizhou, 550025, China

    Qi-Rui Li

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

    J. Jennifer Luangsa-ard

  18. Institute of Marine Biology and Center of Excellence for the Oceans, National Taiwan Ocean University, 2 Pei-Ning Road, Keelung, 20224, Taiwan, Republic of China

    Ka-Lai Pang

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

    Itthayakorn Promputtha

  20. Department Microbial Drugs, Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstrasse 7, 38124, Braunschweig, Germany

    Marc Stadler

  21. German Centre for Infection Research (DZIF), Partner Site Hannover-Braunschweig, 38124, Braunschweig, Germany

    Marc Stadler

Authors
  1. Sajeewa S. N. Maharachchikumbura
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Kevin D. Hyde
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. E. B. Gareth Jones
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. E. H. C. McKenzie
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Jayarama D. Bhat
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Monika C. Dayarathne
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Shi-Ke Huang
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Chada Norphanphoun
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Indunil C. Senanayake
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Rekhani H. Perera
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Qiu-Ju Shang
    View author publications

    You can also search for this author in PubMed Google Scholar

  12. Yuanpin Xiao
    View author publications

    You can also search for this author in PubMed Google Scholar

  13. Melvina J. D’souza
    View author publications

    You can also search for this author in PubMed Google Scholar

  14. Sinang Hongsanan
    View author publications

    You can also search for this author in PubMed Google Scholar

  15. Ruvishika S. Jayawardena
    View author publications

    You can also search for this author in PubMed Google Scholar

  16. Dinushani A. Daranagama
    View author publications

    You can also search for this author in PubMed Google Scholar

  17. Sirinapa Konta
    View author publications

    You can also search for this author in PubMed Google Scholar

  18. Ishani D. Goonasekara
    View author publications

    You can also search for this author in PubMed Google Scholar

  19. Wen-Ying Zhuang
    View author publications

    You can also search for this author in PubMed Google Scholar

  20. Rajesh Jeewon
    View author publications

    You can also search for this author in PubMed Google Scholar

  21. Alan J. L. Phillips
    View author publications

    You can also search for this author in PubMed Google Scholar

  22. Mohamed A. Abdel-Wahab
    View author publications

    You can also search for this author in PubMed Google Scholar

  23. Abdullah M. Al-Sadi
    View author publications

    You can also search for this author in PubMed Google Scholar

  24. Ali H. Bahkali
    View author publications

    You can also search for this author in PubMed Google Scholar

  25. Saranyaphat Boonmee
    View author publications

    You can also search for this author in PubMed Google Scholar

  26. Nattawut Boonyuen
    View author publications

    You can also search for this author in PubMed Google Scholar

  27. Ratchadawan Cheewangkoon
    View author publications

    You can also search for this author in PubMed Google Scholar

  28. Asha J. Dissanayake
    View author publications

    You can also search for this author in PubMed Google Scholar

  29. Jichuan Kang
    View author publications

    You can also search for this author in PubMed Google Scholar

  30. Qi-Rui Li
    View author publications

    You can also search for this author in PubMed Google Scholar

  31. Jian Kui Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  32. Xing Zhong Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  33. Zuo-Yi Liu
    View author publications

    You can also search for this author in PubMed Google Scholar

  34. J. Jennifer Luangsa-ard
    View author publications

    You can also search for this author in PubMed Google Scholar

  35. Ka-Lai Pang
    View author publications

    You can also search for this author in PubMed Google Scholar

  36. Rungtiwa Phookamsak
    View author publications

    You can also search for this author in PubMed Google Scholar

  37. Itthayakorn Promputtha
    View author publications

    You can also search for this author in PubMed Google Scholar

  38. Satinee Suetrong
    View author publications

    You can also search for this author in PubMed Google Scholar

  39. Marc Stadler
    View author publications

    You can also search for this author in PubMed Google Scholar

  40. Tingchi Wen
    View author publications

    You can also search for this author in PubMed Google Scholar

  41. Nalin N. Wijayawardene
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Zuo-Yi Liu.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Table 1

(XLSX 66 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Maharachchikumbura, S.S.N., Hyde, K.D., Jones, E.B.G. et al. Families of Sordariomycetes. Fungal Diversity 79, 1–317 (2016). https://doi.org/10.1007/s13225-016-0369-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13225-016-0369-6

Keywords

Search

Navigation