Abstract
Dothideomycetes comprise a highly diverse range of fungi characterized mainly by asci with two wall layers (bitunicate asci) and often with fissitunicate dehiscence. Many species are saprobes, with many asexual states comprising important plant pathogens. They are also endophytes, epiphytes, fungicolous, lichenized, or lichenicolous fungi. They occur in terrestrial, freshwater and marine habitats in almost every part of the world. We accept 105 families in Dothideomycetes with the new families Anteagloniaceae, Bambusicolaceae, Biatriosporaceae, Lichenoconiaceae, Muyocopronaceae, Paranectriellaceae, Roussoellaceae, Salsugineaceae, Seynesiopeltidaceae and Thyridariaceae introduced in this paper. Each family is provided with a description and notes, including asexual and asexual states, and if more than one genus is included, the type genus is also characterized. Each family is provided with at least one figure-plate, usually illustrating the type genus, a list of accepted genera, including asexual genera, and a key to these genera. A phylogenetic tree based on four gene combined analysis add support for 64 of the families and 22 orders, including the novel orders, Dyfrolomycetales, Lichenoconiales, Lichenotheliales, Monoblastiales, Natipusillales, Phaeotrichales and Strigulales. The paper is expected to provide a working document on Dothideomycetes which can be modified as new data comes to light. It is hoped that by illustrating types we provide stimulation and interest so that more work is carried out in this remarkable group of fungi.
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References
Abarca GH, Ruiz RFC, Mota RMA, Hernandez CIB, Gomez S, Bogale M, Untereiner WA (2011) A new species of Heliocephala from Mexico with an assessment of the systematic position of the anamorph genera Heliocephala and Holubovaniella. Mycologia 103:631–640
Abdel-Aziz FA, Abdel-Wahab MA (2010) Lolia aquatica gen. et sp. nov. (Lindgomycetaceae, Pleosporales), a new coelomycete from freshwater habitats in Egypt. Mycotaxon 114:33–42
Abdel-Wahab A, Jones EGB (2000) Three new marine ascomycetes from driftwood in Australia sand dunes. Mycoscience 41:379–388
Abdollahzadeh J, Goltapeh EM, Javadi A, Shams-Bakhsh M, Zare R, Phillips AJL (2009) Barriopsis iraniana and Phaeobotryon cupressi: two new species of the Botryosphaeriaceae from trees in Iran. Persoonia 23:1–8
Abler SW (2003) Ecology and Taxonomy of Leptosphaerulina spp. associated with Turfgrasses in the United States. Masters Thesis. Blacksburg, Virginia
Acharius E (1798) Lichenographiae. Suecicae Prodromus, Linköping
Aguirre-Hudson B (1991) A taxonomic study of the species referred to the ascomycete genus Leptorhaphis. Bulletin of the British Museum (Natural History). Botany 21:85–192
Aguirre-Hudson B (2009) Celothelium, Cresporhaphis, Leptorhaphis, Rhaphidicyrtis. In: Smith CW et al (eds) The lichens of Great Britain and Ireland. The British Lichen Society, MPG Books Group, Bodmin
Aguirre-Hudson B, Fiol L (1993) A new species of Leptorhaphis (Arthopyreniaceae) on Opuntia from the Balearic Islands. Lichenologist 25:207–210
Aguirre-Hudson B, Hawksworth DL (1987) The circumscription, biology and relationships of the genus Leptorhaphis Körber. In: Peveling E (ed) Progress and problems in Lichenology in the eighties. Bibliotheca Lichenologica 25:249–255
Aguirre-Hudson B, Farkas E, Lokös L (2002) Pyrenolichens of the Hungarian lichen flora I: The genus Leptrorhaphis Körber. Bibl Lichenologica 82:3–18
Ahmed SI, Asad F (1968) Sporormia fimicola sp. nov. and Sporormiella inaequalis sp. nov. from West Pakistan. Sydowia 21:290–294
Ahmed SI, Cain RF (1972) Revision of the genera Sporormia and Sporormiella. Can J Bot 50:419–477
Ainsworth GC, James PW, Hawksworth DL (1971) Ainsworth & Bisby’s dictionary of the fungi, 6th edn. CAB, Kew
Alexopoulos CJ, Mims CW, Blackwell M (1996) Introductory mycology. Wiley, New York
Alias SA, Jones EBG (2009) Marine fungi from mangroves of Malaysia. Institute of Ocean and Earth Sciences, University Malaya, p 108
Alstrup V, Kocourkova J, Kukwa M, Motiejunaite J, von Brackel W, Suija A (2009) The lichens and lichenicolous fungi of South Greenland. Folia Cryptog Estonica 46:1–24
Andjic V, Barber PA, Carnegie AJ, Hardy GSJ, Wingfield MJ, Burgessa TI (2007) Phylogenetic reassessment supports accommodation of phaeophleospora and Colletogloeopsis from eucalypts in kirramyces. Mycol Res 111:1184–1198
Aptroot A (1991a) 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
Aptroot A (1991b) Monoblastia pellucida: a remarkable new lichen species from tropical coastal areas, with comments on the Monoblastiaceae. Bryologist 94:404–406
Aptroot A (1995a) A monograph of Didymosphaeria. Stud Mycol 37:1–160
Aptroot A (1995b) Redisposition of some species excluded from Didymosphaeria (Ascomycetes). Nova Hedwigia 60:325–379
Aptroot A (1998) A world revision of Massarina (Ascomycota). Nova Hedwigia 66:89–162
Aptroot A (1999) Notes on the taxonomy, distribution and ecology of Anisomeridium polypori. Lichenologist 31:641–642
Aptroot A (2002a) Acrocordia. In: Nash TH III, Ryan BD, Gries C, Bungartz F (eds) Lichen flora of the Greater Sonoran Desert Region. I. Lichens unlimited. Arizona State University, Tempe, p 89
Aptroot A (2002b) Mycoporum. In: Nash TH III, Ryan BD, Gries C, Bungartz F (eds) Lichen Flora of the Greater Sonoran Desert Region, vol I. Lichens unlimited. Arizona State University, Tempe, pp 287–288
Aptroot A (2002c) Tomasellia. In: Nash TH III, Ryan BD, Gries C, Bungartz F (eds) Lichen flora of the Greater Sonoran Desert Region, vol I. Lichens unlimited. Arizona State University, Tempe, pp 487–488
Aptroot A (2003) Pyrenocarpous lichens and related non–lichenized ascomycetes from Taiwan. J Hattori Bot Lab 93:155–173
Aptroot A (2006) Mycosphaerella and its anamorphs 2. Conspectus of Mycosphaerella. CBS Biodiversity Series 5:1–231
Aptroot A (2012) A world key to the species of Anthracothecium and Pyrenula. Lichenologist 44:5–53
Aptroot A, Sipman HJM (1993) Musaespora, a genus of pyrenocarpous lichens with campylidia, and other additions to the foliicolous lichen flora of New Guinea. Lichenologist 25:121–135
Aptroot A, Sipman HJM (2001) New Hong Kong lichens, ascomycetes and lichenicolous fungi. J Hattori Bot Lab 91:317–343
Aptroot A, van Iperen AL (1998) New ascomycetes and ascomycete records from Papua New Guinea. Nova Hedwigia 67:481–497
Aptroot A, Diederich P, Sérusiaux E, Sipman HJM (1995) Lichens and lichenicolous fungi of Laing Island (Papua New Guinea). Bibl Lichenologica 57:19–48
Aptroot A, Diederich P, Sérusiaux E, Sipman HJM (1997) Lichens and lichenicolous fungi from New Guinea. Bibl Lichenologica 64:1–220
Aptroot A, Lücking R, Sipman HJM, Umaña L, Chaves JL (2008) Pyrenocarpous lichens with bitunicate asci: a first assessment of the lichen biodiversity inventory in Costa Rica. Bibl Lichenologica 97:1–162
Ariyawansa HA, Jones EBG, Suetrong S, Alias SA, Kang JC, Hyde KD (2013a) Halojulellaceae a new family of the order Pleosporales. Phytotaxa 130:14–24
Ariyawansa HA, Maharachchikumbura SSN, Karunarathne SC, Chukeatirote E, Bahkali AH, Kang JC, Bhat JD, Hyde KD (2013b) Deniquelata barringtoniae from Barringtoniaasiatica, associated with leaf spots of Barringtonia asiatica. Phytotaxa 105:11–20
Arnaud G (1913) Sur les genres Zopfia, Richonia et Caryospora. Bull Trimest Soc Mycol Fr 29:253–260
Arnaud G (1915) Notes mycologiques (G. Isaria et Parodiopsis). Bull Soc Mycol Fr 31(1):20–23
Arnaud G (1918) Les Astérinées. Ann Ecole Nat Agric Montpellier nouv Série 16:1–288
Arnaud G (1920) La famille des Parodiellinacées (Pyrénomycètes). C R Acad Sci 170:202–204
Arnaud G (1921) Les Astérinées: II. Études sur les champignons (Parodiellinacées, inclus Erysiphées). Ann Epiphyties 7:1–115
Arnaud G (1925) Les Asterinees. IVe Partie. (Études sur la Systématique des champignons Pyrénomycetes). Annales Des Sciences Naturelles. Botanique 7:643–723
Arnaud G (1930) Les Astérinées. V. Études sur les champignons parasites: Caliciacées, Hémisphériacées, etc. Ann Épiphyties 16:235–302
Arnaud G (1931) Traité de PathologieVégétal, Paris, vol. 1, 2
Arnold F (1858) Die Lichenen des fränkischen Jura. Flora 41:81–95
Arzanlou M, Groenewald JZ, Gams W, Braun U, Shin H-D, Crous PW (2007) Phylogenetic and morphotaxonomic revision of Ramichloridium and allied genera. Stud Mycol 58:57–93
Atkinson GF (1902) New genera of the higher fungi. Bot Gaz 34(1):36–43
Auerswald B (1866) Delitschia nov. gen. e grege Sphaeriacearum simplicium. Hedwigia 5:49–64
Aveskamp MM, de Gruyter J, Crous PW (2008) Biology and recent developments in the systematic of Phoma, a complex genus of major quarantine significance. Fungal Divers 31:363–382
Aveskamp MM, de Gruyter H, Woudenberg J, Verkley G, Crous PW (2010) Highlights of the Didymellaceae: a polyphasic approach to characterise Phoma and related pleosporalean genera. Stud Mycol 65:1–60
Barnes I, Crous PW, Wingfield BD, Wingfield MJ (2004) Multigene phylogenies reveal that red band needle blight of Pinus is caused by two distinct species of Dothistroma, D. septosporum and D. pini. Stud Mycol 50:551–565
Barr ME (1961) Northern pyrenomycetes. II. Gaspesian Park. Can J Bot 39:307–325
Barr ME (1968) The Venturiaceae in North America. Can J Bot 46(6):799–864
Barr ME (1975) The genus Ostreichnion. Mycotaxon 3:81–88
Barr ME (1976) Perspectives in the Ascomycotina. Mem N Y Bot Gard 28:1–8
Barr ME (1979a) A classification of Loculoascomycetes. Mycologia 71:935–957
Barr ME (1979b) On the Massariaceae in North America. Mycotaxon 9:17–37
Barr ME (1980) On the family Tubeufiaceae (Pleosporales). Mycotaxon 12:137–167
Barr ME (1981) The genus Curreya: an example of taxonomic confusion in the Ascomycetes. Mycologia 73:599–609
Barr ME (1982) On the Pleomassariaceae (Pleosporales) in North America. Mycotaxon 15:349–383
Barr ME (1983a) Muriform ascospores in class Ascomycetes. Mycotaxon 18:149–157
Barr ME (1983b) The ascomycete connection. Mycologia 75:1–13
Barr ME (1987a) Prodomus to class Loculoascomycetes. Publ. by theauthor, Amherst
Barr ME (1987b) New taxa and combinations in the Loculoascomycetes. Mycotaxon 29:501–505
Barr ME (1987c) Prodromus to class Loculoascomycetes. University of Massachusetts, Amherst
Barr ME (1989a) Some unitunicate taxa excluded from Didymosphaeria. Stud Mycol 31:23–27
Barr ME (1989b) The genus Dothidotthia (Botryosphaeriaceae) in North America. Mycotaxon 34:517–526
Barr ME (1990a) Melanommatales (Loculoascomycetes). N Am Flora Ser II 13:1–129
Barr ME (1990b) Prodromus to nonlichenized, pyrenomycetous members of class Hymenoascomycetes. Mycotaxon 39:43–184
Barr ME (1990c) Some dictyosporous genera and species of Pleosporales in North America. Mem N Y Bot Gard 62:1–92
Barr ME (1990d) Melanommatales (Loculoascomycetes). N Am Flora 2:1–129
Barr ME (1992a) Additions to and notes on the Phaeosphaeriaceae (Pleosporales, Loculoascomycetes). Mycotaxon 43:371–400
Barr ME (1992b) Notes on the Lophiostomataceae (Pleosporales). Mycotaxon 45:191–221
Barr ME (1993a) Notes on the Pleomassariaceae. Mycotaxon 49:129–142
Barr ME (1993b) Redisposition of some taxa described by J. B. Ellis. Mycotaxon 46:4576
Barr ME (1996) Planistromellaceae, a new family in the Dothideales. Mycotaxon 60:433–442
Barr ME (1997) Notes on some ‘dimeriaceous’ fungi. Mycotaxon 64:149–171
Barr ME (2000a) Notes on coprophilous bitunicate ascomycetes. Mycotaxon 76:105–112
Barr ME (2000b) Teichosporaceae, another family in the Pleosporales. Mycotaxon 82:373–389
Barr ME (2001) Montagnulaceae, a new family in Pleosporales, and lectotypification of Didymosphaeriella. Mycotaxon 77:193–200
Barr ME (2002) Teichosporaceae, another family in the Pleosporales. Mycologia 82:373–389
Barr ME (2003) The affinities of Thyridaria. Mycotaxon 88:271–278
Barr ME, Blackwell M (1980) A new genus in the Lophiaceae. Mycologia 72:1224–1227
Barr ME, Huhndorf SM (2001) Loculoascomycetes. In: McLaughlin DJ, McLaughlin EG, Lemke PA (eds) The mycota VII, part A. Systematics and evolution. Springer Verlag, Berlin, pp 283–305
Batista AC (1957) The Atichiales in Pernambuco. Anais Soc Biol Pernamb 15:311–332
Batista AC (1959) Monografia dos fungos Micropeltaceae. Publicações Inst Micol Univ Recife 56:1–519
Batista AC (1960) Lembopodia, Yamamotoa e Peresiopsis, novos gêneros de Asterinaceae. Publ IMUR, Recife 291:1–35
Batista AC, Cavalcante W d A (1967) Acanthorus n.gen. e outros Coelomycetes de fumagina. Atas do Instituto de Micologia. Univ Pernambuco, Recife 4:245–254
Batista AC, Ciferri R (1957) Two previously undescribed cucurbitariaceous fungi. Atti dell’Istituto. Botanico dell’Universita di Pavia 5(15):63–66
Batista AC, Ciferri R (1963) The sooty-molds of the family Asbolisiaceae. Quaderni. Laboratorio Crittogamico, Istituto Botanico della Università di Pavia 31:7, p 229
Batista AC, Maia HDS (1965) Caprettia, novo genero de ascoliquen, em homenagem ao micologo venezuelano, Corrado Capretti. Univ Fed Pernambuco Inst Micol Atas 2:375–382
Batista AC, Nascimento ML (1957) Alguns novos fungos imperfeitos do complex de fumagina. An Soc Biol Pernambuco 15(2):345–353
Batista AC, Maia HS, Farr ML (1958) Novos generos e novasespecies de fungos Asterinaceae. Rev Biol Lisbõa 1(3–4):287–298
Batista AC, Bezerra JL, de Cavalcante W d A, da Silva MH (1963) Mycerema e outros novos gêneros de Stomiopeltoideae, da familia Micropeltaceae. Publicações Inst Micol Univ Recife 392:1–40
Batzer JC, Mercedes Diaz Arias M, Harrington TC, Gleason ML, Groenewald JZ, Crous PW (2008) Four species of Zygophiala (Schizothyriaceae, Capnodiales) are associated with the sooty blotch and flyspeck complex on apple. Mycologia 100:246–258
Behrend G (1890) Ueber Trichomycosis nodosa (Juhel-Renoy); Piedra (Osorio). 27:464–467
Bensch K, Braun U, Groenewald JZ, Crous PW (2012) The genus Cladosporium. Stud Mycol 72:1–401
Berkeley MJ (1845) Decades of fungi. Decades III-VII. Australian fungi. London J Bot 4:42–73
Berkeley MJ (1876) Notices of North American fungi. Grevillea 4(31):105–106
Berkeley MJ, Broome CE (1850) Notices of British fungi (438–501). Ann Mag Nat Hist 5:455–466
Berlese AN (1896) Icones fungorum. II. fasc: 29–68
Berlese A (1900) Icones Fungorum. Padova 2:216
Bin S (2003) Goosia, a new genus of Englerulaceae. Mycotaxon 87:413–415
Bisby GR (1923) The literature on the classification of the Hysteriales. Trans Br Mycol Soc 8:176–189
Bizzozero G (1885) Funghi Veneti novi vel critici. Atti dell’Istituto Veneto Scienze 3:303
Blackwell M, Gilbertson RL (1985) Quasiconcha reticulata and its anamorph from conifer roots. Mycologia 77:50–54
Blain WL (1927) Comparative morphology of dothideaceous and kindred stromata. Mycologia 19(1):13
Boedijn KB (1961) Myriangiales from Indonesia. Persoonia 2:63–75
Boehm E, Mugambi G, Miller A, Huhndorf S, Marincowitz S, Spatafora J (2009a) A class–wide phylogenetic assessment of Dothideomycetes. Stud Mycol 64:1–15S10
Boehm EWA, Mugambi G, Miller AN, Huhndorf S, Marincowitz S, Schoch CL, Spatafora JW (2009b) A phylogenetic reappraisal of the Hysteriaceae, Mytilinidiaceae & Gloniaceae with keys to world species. Stud Mycol 64:49–83
Boehm EWA, Schoch CL, Spatafora JW (2009c) On the evolution of the Hysteriaceae and Mytilinidiaceae (Pleosporomycetidae, Dothideomycetes, Ascomycota) using four nuclear genes. Mycol Res 113:461–479
Boerema GH (1997) Contributions towards a monograph of Phoma(Coelomycetes) - V. Subdivision of the genus in sections. Mycotaxon 64:321–333
Boerema GH, De Gruyter J, Noordeloos ME, Hamers MEC (2004) Phomaidentification manual. Differentiation of specific and infraspecific taxa in culture. CABI Publishing, United Kingdom
Boise JR (1985a) An amended description of Trematosphaeria. Mycologia 77:230–237
Boise JR (1985b) New combinations in the Pleomassariaceae and the Massarinaceae. Mycotaxon 22:477–482
Boissière JC, Montavont JP (1998) Lichens de France (XI): Epigloea filifera Döbb. et Lobaria amplissima (Scop.) Forss. dans sa forme avec céphalodies. Bull d’Informations l’Assoc Française Lichénologie 23(1):1–6
Bonifaz A, Badali H, de Hoog GS, Cruz M, Araiza J (2008) Tinea nigra by Hortaea werneckii, a report of 22 cases from Mexico. Stud Mycol 61:77–82
Boonmee S, Zhang Y, Chomnunti P, Chukeatirote E, Tsui CKM, Bahkali AH, Hyde KD (2011) Revision of lignicolous Tubeufiaceae based on morphological reexamination and phylogenetic analysis. Fungal Divers 51:63–102
Boonmee S, KoKo TW, Chukeatirote E, Hyde KD, Chen H, Cai L, McKenzie EHC, Jones EBG, Kodsueb R, Hassan BA (2012) Two new Kirschsteiniothelia species with Dendryphiopsis anamorphs cluster in Kirschsteiniotheliaceae fam. nov. Mycologia 104:698–714
Boonmee et al. (2013) Tubeufiales, ord. nov., integrating sexual and asexual generic names (in prep)
Borse BD (1987) Marine fungi from India, V. Curr Sci 56:1109–1111
Bose SK (1961) Studies on Massarina Sacc. and related genera. Phytopathol Z 41:151–213
Brandriff H (1936) The development of the ascocarp of Acrospermum compressum. Mycologia 28:228–235
Braun U (1995) A monograph of Cercosporella, Ramularia and allied genera (Phytopathogenic Hyphomycetes). Vol. 1. IHW–Verlag, Eching
Braun U (1998) A monograph of Cercosporella, Ramularia and allied genera (Phytopathogenic Hyphomycetes). Vol. 2. IHW–Verlag, Eching
Braun U, Crous PW, Dugan F, Groenewald JZ, de Hoog GS (2003) Mycol Prog 2:3–18
Braun U, Crous PW, Schubert K, Shin HD (2010) Some reallocations of Stenella species in Zasmidium. Schlechtendalia 20:99–104
Braun-Falco O, Plewig G, Wolff HH, Burgdorf WHC (2000) Dermatology, 2nd edn. Springer Verlag, Berlin
Brefeld O (1891) Unter suchungen aus dem gesammtge biete der Mycologie. 10. Ascomyceten. II. Münster. p 378
Breuss O (2001) Flechten aus Costa Rica II. Linzer Biologische Beitraege 33:1025–1034
Bricaud O, Roux C, Ménard T, Coste C (1993) Champignons lichénisés et lichénicoles de la France méridionale: espèces nouvelles et intéressantes (8). Bull Société Linnéenne de Provence 44:99–109
Burney DA, Robinson GS, Burney LP (2003) Sporormiella and the late Holocene extinctions in Madagascar. Proc Natl Acad Sci U S A 100:10800–10805
Bussaban B, Lumyong S, Lumyong P, Seelanan T, Park D, McKenzie E, Hyde K (2005) Molecular and morphological characterization of Pyricularia and allied genera. Mycologia 97(5):1002–1011
Cai L, Guo XY, Hyde KD (2008) Morphological and molecular characterisation of a new anamorphic genus Cheirosporium, from freshwater in China. Persoonia 20:53–58
Cain RF (1934) Studies of coprophilous Sphaeriales in Ontario. Univ Toronto Stud: Biol Ser 38:1–126
Cain RF (1956) Studies on coprophilous ascomycetes. II. Phaeotrichum, a new cleistocarpous genus in a new family, and its relationships. Can J Bot 34:675–684
Calatayud V, Navarro-Rosinés P (1998) Weddellomyces xanthoparmeliae sp. nov. and additions to the chorology of other species of the genus. Mycotaxon 69:503–514
Calatayud V, Triebel D (2003) Three new species of Stigmidiums. l. (lichenicolous ascomycetes) on Acarospora and Squamarina. Lichenologist 35(2):103–116
Calatayud V, Sanz MJ, Aptroot A (2001) Lichenopyrenis galligena (Pleomassariaceae), a new genus of gall-forming lichenicolous fungi on Leptochidium. Mycol Res 105(5):634–637
Câmara MPS, Palm ME, van Berkum P, O’Neill NR (2002) Molecular phylogeny of Leptosphaeria and Phaeosphaeria. Mycologia 94:630–640
Câmara MP, Ramaley AW, Castlebury LA, Palm ME (2003) Neophaeosphaeria and Phaeosphaeriopsis, segregates of Paraphaeosphaeria. Mycol Res 107:516–522
Campbell J, Ferrer A, Raja HA, Sivichai S, Shearer CA (2007) Phylogenetic relationships among taxa in the Jahnulales inferred from 18S and 28S nuclear ribosomal DNA sequences. Can J Bot 85:873–882
Cannon PF, Kirk PM (2007) Fungal families of the world. CABI Bioscience, Wallingford
Carnegie AJ, Pegg GS, White D, Burgess TI (2011) Species within Mycosphaerellaceae and Teratosphaeriaceae from eucalypts in eastern Australia. Australas Plant Pathol 40:366–384
Castlebury L, Crane J, Huhndorf S (1995) A new species of Rhytidenglerula from Everglades National Park, Florida. Mycotaxon 54:461–463
Cesati V, de Notaris G (1863) Schema di classificazione deglesferiacei italici aschigeri piu’ o meno appartenenti al genere Sphaeria nell’antico significato attribuitoglide Persono. Comm Soc crittog Ital 1:177–420
Chatmala IR, Valyase R, Tanticharoen M (2002) Anamorph/teleomorph connections of marine Ascomycota. In: Hyde KD (ed) Fungi in marine environments. Fungal Diversity Press, Hong Kong, pp 59–68
Chaverri P, Gazis RO (2010) Perisporiopsis lateritia, a new species on decaying leaves of Hevea spp. from the Amazon basin in Peru. Mycotaxon 113:163–169
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
Checa J, Shoemaker RA, Umaña L (2007) Some new hysteriaceous fungi from Costa Rica. Mycologia 99:285–290
Cheewangkoon R, Groenewald JZ, Summerell BA, Hyde KD, To-anun C, Crous PW (2010) Myrtaceae, a cache of fungal biodiversity. Persoonia 23:55–85
Chesters CGC, Bell A (1970) Studies in the Lophiostomataceae Sacc. Mycol Pap 120:1–55
Chevallier FF (1826) Flore générale des environs de Paris, vol I. Ferra Librairie-Editeur, Paris
Chilvers MI, Rogers JD, Dugan FM, Stewart JE, Chen W, Peever TB (2009) Didymella pisi sp. nov., the teleomorph of Ascochyta pisi. Mycol Res 113:391–400
Choisy M (1955) Systematique des Roccellaceae, famille de lichens ascomycètes ascoloculaires. Bull Trimest Soc Mycol Fr 71(4):312–324
Chomnunti P, Schoch CL, Aguirre-Hudson B, KoKo TW, Hongsanan S, Jones EBG, Kodsub R, Chukeatirote E, Bahkali AH, Hyde KD (2011) Capnodiaceae. Fungal Divers 51:103–134
Chung KR (2011) Elsinoë fawcettii and Elsinoë australis: the fungal pathogens causing citrus scab. Mol Plant Pathol 12:123–135
Ciferri R, Tomaselli R (1953) Tentative mycolichenes classification. Atti dell’Istituto Botanico della Università e Laboratorio Crittogamico di Pavia Ser. 5 10(1):25–84
Ciferri R, Batista AC, Campos CA (1956) Taxonomy of Piedraia hortaiand systematic position of the Piedraiaceae family. Publções Inst Micol Recife 45:1–9
Clements FE, Shear CL (1931) Genera of fungi, edn 2. i–vii, 58 plates. H.W. Wilson Company, USA, New York, p 496
Cole MS, Hawksworth DL (2004) Lichenoconium christiansenii sp. nov. from Nodobryoriaabbreviata (Parmeliaceae) in the Pacific Northwest, with a key to the known lichenicolous species. Lichenologist 36:1–6
Conde BD, Pitkethley RN, Smith ESC, Kulkarni VJ, Thiagalingam K, Ulyatt LL, Connelly ML, Hamilton DA (1997) Disease notes or new records: identification of mango scab caused by Elsinoё mangiferae in Australia. Australas Plant Pathol 26:131
Cooke WB (1983) Coniothyriaceae. Rev Biol (Lisbon) 12:289
Cooke MC, Hawksworth DL (1970) A preliminary list of families proposed for the fungi. Mycol Pap 121:1–86
Coppins BJ (1988) Notes on the genus Arthopyrenia in the British Isles. Lichenologist 20:305–325
Coppins BJ (2002) Checklist of lichens of Great Britain and Ireland. British Lichen Society, p 87
Coppins B, Kondratyuk SY (1995) Stygiomyces and Pseudonitschkia: two new genera of lichenicolous fungi. Edinb J Bot 52:229–236
Corda ACJ (1838) Patellariaceae in Icones Fungorum hucusque Cognitorum 2:1–43
Corda ACJ (1842) Abbildungen der Pilze und Schwaemme. Icones Fungorum, Hucusque Cognitorum 5:34
Corlett M (1981) A taxonomic survey of some species of Didymella and Didymella–like species. Can J Bot 59:2016–2042
Cortinas MN, Koch N, Thain J, Wingfield BD, Wingfield MJ (2004) First record of the Eucalyptus stem canker pathogen, Coniothyrium zuluense from Hawaii. Australas Plant Pathol 33:309–312
Cortinas MN, Crous PW, Wingfield BD, Wingfield MJ (2006) Multi–gene phylogenies and phenotypic characters distinguish two species within the Colletogloeopsis zuluensis complex associated with Eucalyptus stem cankers. Stud Mycol 55:133–146
Crane JL (1971) Illinois fungi. 1. Chaetosticta. Can J Bot 49:31–34
Crane JL, Shearer CA (1991) A nomenclator of Leptosphaeria V. Cesati & G. de Notaris (Mycota, Ascomycotina, Loculoascomycetes). Bull Illinois State Nat Hist Surv 34:1–355
Crivelli PG (1983) Über die heterogene Ascomycetengattung Pleospora Rabh.: Vorschlag für eine Aufteilung. Abh. Eidgenössischen Technischen Hochschule Zürich 7318: 213 pp
Crous PW (1998) Mycosphaerella spp. and their anamorphs associated with leaf spot diseases of Eucalyptus. Mycol Memories 21:1–170
Crous PW, Braun U (2003) Mycosphaerella and its anamorphs.1. Names published in Cercospora, Passalora. CBS Biodivers Ser 1:1–571
Crous PW, Kendrick WB (1994) Arnaudiella eucalyptorum sp. nov. (Dothideales, Ascomycetes) and its hyphomycetous anamorph. Can J Bot 72:59–64
Crous PW, Aptroot A, Kang JC, Braun U, Wingfield MJ (2000) The genus Mycosphaerella and its anamorphs. Stud Mycol 45:107–121
Crous PW, Kang JC, Braun U (2001) A phylogenetic redefinition of anamorph genera in Mycosphaerella based on ITS rDNA sequence and morphology. Mycologia 93:1081–1101
Crous PW, Groenewald JZ, Aptroot A, Braun U, Xavier M, Carlier J (2003a) Integrating morphological and molecular data sets in Mycosphaerella, with specific reference to species occurring on Musa. In: Jacome L, Lepoivre P, Marin D, Ortiz R, Romero R, Escalant JV (eds) Mycosphaerella leaf spot diseases of bananas: present status and outlook. Proceedings of the Second International Workshop on Mycosphaerella leaf spot diseases of bananas, 20–23 May 2002, San José, Costa Rica. INIBAP. pp 43–57
Crous PW, Groenewald JZ, Gams W (2003b) Eyespot of cereals revisited: ITS phylogeny reveals new species relationships. Eur J Plant Pathol 109:841–850
Crous PW, Groenewald JZ, Wingfield MJ, Aptroot A (2003c) The value of ascospore septation in separating Mycosphaerella from Sphaerulina in the Dothideales: a Saccardoan myth? Sydowia 55:136–152
Crous PW, Groenewald JZ, Mansilla JP, Hunter GC, Wingfield MJ (2004) Phylogenetic reassessment of Mycosphaerella spp. and their anamorphs occurring on Eucalyptus. Stud Mycol 50:195–214
Crous PW, Slippers B, Wingfield MJ, Rheeder J, Marasas WFO, Philips AJL, Alves A, Burgess TI, Barber PA, Groenewald JZ (2006) Phylogenetic lineages in the Botryosphaeriaceae. Stud Mycol 55:235–253
Crous PW, Braun U, Groenewald JZ (2007a) Mycosphaerella is polyphyletic. Stud Mycol 58:1–3
Crous PW, Braun U, Schubert K, Groenewald JZ (2007b) Delimiting Cladosporium from morphologically similar genera. Stud Mycol 58:33–56
Crous PW, Schubert K, Braun U, de Hoog GS, Hocking AD, Shin HD, Groenewald JZ (2007c) Opportunistic, human-pathogenic species in the Herpotrichiellaceae are phenotypically similar to saprobic or phytopathogenic species in the Venturiaceae. Stud Mycol 58:185–217
Crous PW, Braun U, Wingfield MJ, Wood AR, Shin HD, Summerell BA, Alfenas AC, Cumagun CJR, Groenewald JZ (2009a) Phylogeny and taxonomy of obscure genera of microfungi. Persoonia 22:139–161
Crous PW, Schoch CL, Hyde KD, Wood AR, Gueidan C, de Hoog GS, Groenewald JZ (2009b) Phylogenetic lineages in the Capnodiales. Stud Mycol 64:17–47
Crous PW, Summerell BA, Carnegie AJ, Wingfield MJ, Groenewald JZ (2009c) Novel species of Mycosphaerellaceae and Teratosphaeriaceae. Persoonia 23:119–145
Crous PW, Summerell BA, Carnegie AJ, Wingfield MJ, Hunter GC, Burgess TI, Andjic V, Barber PA, Groenewald JZ (2009d) Unravelling Mycosphaerella: do you believe in genera? Persoonia 23:99–118
Crous PW, Tanaka K, Summerell BA, Groenewald JZ (2011) Additions to the Mycosphaerella complex. IMA Fungus 2:49–64
Crous PW, Summerell BA, Shivas RG, Burgess TI, Decock CA (2012) Fungal Planet description sheets: 107–127 Persoonia 28:138–182
Crous PW, Braun U, Hunter GC, Wingfield MJ, Verkley GJM, Shin HD, Nakashima C, Groenewald JZ (2013) Phylogenetic lineages in Pseudocercospora. Stud Mycol 75:37–114
Cunnell GJ (1961) Stagonospora macropycnidia sp. nov. Trans Br Mycol Soc 55:87–90
Cuomo V, Vanzanella F, Fresi E, Cinelli F, Mazzella L (1985) Fungal flora of Posidonia oceanica and its ecological significance. Trans Br Mycol Soc 84:35–40
Currah RS (1985) Taxonomy of the Onygenales: Arthrodermataceae, Gymnoascaceae, Myxotrichaceae and Onygenaceae. Mycotaxon 24:103–105
Currah RS (1994) Peridial morphology and evolution in the Prototunicatea scomycetes. In: Hawksworth DL (ed) Ascomycete systematics: problems and perspectives in the nineties. Plenum Press, New York, pp 281–293
Cybertruffle (2013) http://www.cybertruffle.org.uk/spegazzini/eng/002103a.html
Dai DQ, Jayarama Bhat D, Liu JK, Chukeatirote E, Zhao RL, Hyde KD (2012) Bambusicola, a new genus from bamboo with asexual and sexual morphs. Cryptog Mycolog 33:363–379
Damm U, Verkley GJM, Crous PW, Fourie PH, Haegi A, Riccioni L (2008) Novel Paraconiothyrium species on stone fruit trees and other woody hosts. Persoonia 20:9–17
Danilo BP Jr, Honorato J, Nicoli A Jr, Hora BT, Braganca CAD, Pereira OL (2012) Phylogenetic placement of the genus Anhellia and the description of A. nectandrae sp. nov. Mycologia 104:1291–1298
Darker GD (1963) A new genus of the Lophiaceae. Can J Bot 41:1383–1388
David JC, Hawksworth DL (1991) Validation of six family names of lichenized ascomycetes. Systema Ascomycetum 10:13–16
de Gruyter JD, Aveskamp MM, Woudenberg JHC, Verkley GJM, Groenewald JZ, Crous PW (2009) Molecular phylogeny of Phoma and allied anamorph genera: towards a reclassification of the Phoma complex. Mycol Res 113:508–519
de Gruyter JD, Woudenberg JH, Aveskamp MM, Verkley GJ, Groenewald JZ, Crous PW (2010) Systematic reappraisal of species in Phoma section Paraphoma, Pyrenochaeta and Pleurophoma. Mycologia 102:1066–1081
de Gruyter JD, Woudenberg JHC, Aveskamp AA, Verkley GJM, Groenewald JZ, Crous PW (2012) Redisposition of Phoma-like anamorphs in Pleosporales. Stud Mycol 75:1–36
de Hoog GS, Oorschot CAN van, Hijwegen T (1983) Taxonomy of the Dactylaria complex. II. Dissoconium gen. nov. and Cordana preuss. Proceedings of the Koninklijke Nederlandse Akademie van Wetenschappen, Series C 86:197–206
de Hoog GS, Guarro J, Gené J, Figueras MJ (2000) Atlas of Clinical Fungi. 2nd edn. Centraalbureau voor Schimmelcultures, Utrecht, Netherlands, and Universitat Rovira I Virgili, Reus, Spain
de Liyanage AS, Jayasinghe CK, Liyanage NIS, Jayaratne R (1986) Corynespora leaf spot disease of rubber (Hevea brasiliensis) a new record. J Rubber Res Inst Sri Lanka 65:47–50
de Notaris G (1845) Micromycetes Italici novi vel minus cogniti. V Mem R Acc Sci Torino 2(10):333–350
Deighton FC (1976) Studies on Cercospora and allied genera. VI. Pseudocercospora Speg., Pantospora Cif. and Cercoseptoria Petr. Mycol Pap 140:1–168
Del Prado R, Schmitt I, Kautz S, Palice Z, Lücking R, Lumbsch HT (2006) Molecular data place Trypetheliaceae in Dothideomycetes. Mycol Res 110:511–520
Dennis RWG (1968) British ascomycetes, 2nd edn. J. Cramer, Vaduz
Dennis RWG (1978) British ascomycetes, 3rd edn. J. Cramer, Vaduz
Desmazières JBHJ (1841) Huitième notice sur quelques plantes cryptogames, la plupart inédites, récemment découvertes en France. Ann Sci Nat Bot 15:129–146
Desmazières JBHJ (1849) Dix–septième notice sur les plantes cryptogames récemment découvertes en France. Ann Sci Nat Bot Ser 3(11):360
Dixon LJ, Schlub RL, Pernezny K, Datnoff LE (2009) Host specialization and phylogenetic diversity of Corynespora cassiicola. Phytopathology 99:1015–1027
Döbbeler P (1984) Symbiosen zwischen Gallertalgen und Gallertpilzen der Gattung Epigloea (Ascomycetes). In: Hertel H, Oberwinkler F (eds) Beitrage zur Lichenologie. Festscrift J. Poelt. Beiheft zur Nova Hedwigia 79. J. Cramer, Vaduz, pp 203–239
Döbbeler P (1994) Epigloea urosperma (Ascomycetes) ein neuer Flechtenparasit. Sendtnera 2:277–282
Doidge EM (1942) South African Microthyriaceae. Bothalia 4:273–344
Doilom M, Liu JK, Jaklitsch WM, Ariyawansa H, Wijayawardene NN, Chukeatirote E, Zhang M, McKenzie EHC, Geml J, Voglmayr H, Hyde KD (2013) An outline of the family Cucurbitariaceae. Sydowia 65(1):167–192
Dong J, Chen W, Crane JL (1998) Phylogenetic studies of the Leptosphaeriaceae, Pleosporaceae and some other loculoascomycetes based on nuclear ribosomal DNA sequences. Mycol Res 102(2):151–156
Duby JE (1862) Memoire sur la tribu des Hysterinees de la famille des Hypoxylees (Pyrenomycetes). Mem Soc Phys Hist Nat Genève 16:15–70
Dugan JE, Jaramillo E, Hubbard DM, Contreras H, Duarte C (2004) Competitive interactions in macroinfaunal animals of exposed sandy beaches. Oecologia 139:630–640
Durieu C, Montagne JFC (1956) Sylloge genereum Specierumque Cryptoamarum. Bailliére et Fils, Paris, p 229
Durieux M (1963) Comment. Soc Crittogam Ital 1:224
Eaton RA, Jones EBG (1971) New fungi on timber from water-cooling towers. Nova Hedwigia 19(779):783
Ellis MB (1949) Tetraploa. Trans Br Mycol Soc 32:246–251
Ellis MB (1971) Dematiaceous hyphomycetes. Commonwealth Mycological Institute, Kew
Ellis JP (1976) British Microthyrium species and similar fungi. Trans Br Mycol Soc 67(3):381–394
Ellis JP (1980) The genus Morenoina in Britain. Trans Br Mycol Soc 74:297–307
Ellis JB, Everhart BM (1892) The North American pyrenomycetes. Newfield, NJ
Eriksson OE (1967) On graminicolous pyrenomycetes from Fennoscandia. I, II, III. Ark Bot Ser 26:339–466
Eriksson OE (1981) The families of bitunicate ascomycetes. Nord J Bot 1(6):800
Eriksson OE (1982) Outline of the ascomycetes. Mycotaxon 15:203–248
Eriksson OE (1994) Problems in the classification of fissitunicate ascomycetes. In: Hawksworth DL (ed) Ascomycete systematics. Problems and perspectives in the nineties. NATO ASI, vol 269. Plenum Press, New York and London, pp 341–345
Eriksson OE (2005) Outline of Ascomycota, The present classification contains all accepted genera and higher taxa above the generic level in phylum Ascomycota. Myconet 11:1–113
Eriksson OE (2006) Outline of Ascomycota. Myconet 12:1–88
Eriksson OE, Hawksworth DL (1986a) Notes on ascomycete systematics. Nos. 1–224. Syst Ascomycetum 5:113–174
Eriksson OE, Hawksworth DL (1986b) Outline of the ascomycetes. Syst Ascomycetum 5:185–324
Eriksson OE, Hawksworth DL (1987) Outline of the ascomycetes. Syst Ascomycetum 6:259–337
Eriksson OE, Hawksworth DL (1991) Outline of the Ascomycetes 1990. Systema Ascomycetum 1–4 (1982–1985) 9: 39–271
Eriksson OE, Hawksworth DL (1992) Notes on ascomycete systematics 1294–1417. Syst Ascomycetum 11:49–82
Eriksson OE, Hawksworth DL (1993) Notes on ascomycete systematics – Nos 1418–1529. Syst Ascomycetum 11:163–194
Eriksson OE, Hawksworth DL (2003) Saccharicola, a new genus for two Leptosphaeria species on sugar cane. Mycologia 95:426–433
Eriksson OE, Yue JZ (1990) Notes on bambusicolous pyrenomycetes. Mycotaxon 38:201–220
Eriksson OE, Baral HO, Currah RS, Hansen K, Kurtzman CP, Rambold G, Laessøe T (2004) Outline of Ascomycota. Myconet 10:1–99
Ertz D, Lawrey JD, Common RS, Diederich P (2013) Molecular data resolve a new order of Arthoniomycetes sister to the primarily lichenized Arthoniales and composed of black yeasts, lichenicolous and rock-inhabiting species. Fungal Diversity 1–25
Etayo J (2002) Catálogo de líquenes y hongos liquenícolas del Parque Natural de Bértiz (Navarra, España). Bull Soc Linnéenne Provence 53:155–171
Etayo J, Sancho LG (2008) Hongos liquenícolas del sur de Sudamérica, especialmente de Isla Navarino (Chile). Bibl Lichenologica 98:1–302
Etayo J, Van den Boom PPG (2006) Some lichenicolous fungi from Guatemala, with the description of a new species. Herzogia 19:191–197
Fallah PM, Shearer CA (2001) Freshwater ascomycetes: new or noteworthy species from north temperate lakes in Wisconsin. Mycologia 93:566–602
Farr ML (1979) The didymosporous dimeriaceous fungi described on Asteraceae. Mycologia 71:243–803
Farr DF, Rossman AY (2012) Fungal databases, systematic mycology and microbiology laboratory, ARS, USDA. http://nt.ars-grin.gov/fungaldatabases/Retrieved 25 October 2011
Farr DF, Bills GF, Chamuris GP, Rossman AY (1989) Fungi on plants and plant products in the United States. APS Press, St. Paul
Faull JL, Olejnik I, Ingrouille M, Reynolds D (2002) A reassessment of the taxonomy of some tropical sooty moulds. Tropical mycology volume 2. Micromycetes. CABI, UK, pp 33–40
Ferrer A, Miller AN, Shearer CA (2011) Minutisphaera and Natipusilla: two new genera of freshwater Dothideomycetes. Mycologia 103:411–423
Fink B (1910) The lichens of Minnesota. Contributions from the U.S. National Museum. 14:1–269
Fink B (1913) The nature and classification of lichens II. The lichen and its algal host. Mycologia 5:111
Fisher PJ, Webster J (1992) A Trematosphaeria endophyte from rice roots and its Zalerion anamorph. Nova Hedwigia 54:77–81
Fonseca O, Leão AE d A (1928) Sobre os cogumelos da piedra brazileira. Mem Inst Oswaldo Cruz 21(suppl 4):124–127
Foucard T (1992) Notes on the corticolous Arthopyrenia–species in Sweden. Graphis Scripta 4:49–60
Fries EM (1818) Observationes mycologicae. Gerh. Bonnier, Copenhagen 2:347–351
Fries EM (1823) Systema mycologicum, vol.2, section II,. 620 pages Gryphiswaldiae
Fuckel L (1870) Beiträge zur Kenntniss der Rheinischen Pilze. Jahrbücher Nassauischen Vereins Naturkunde 23–24:1–459
Fuckel KWGL (1871) Symbolae mycologicae. Beiträgezur Kenntniss der Rheinischen Pilze. Erster Nachtrag. Jahrbücher Nassauischen Vereinsfür Naturkunde 25–26:25
Gams W (1999) Report of the committee for fungi: 8. Taxon 48:807–810
Gamundí IJ, Spinedi MA (1985) Phaneromyces Speg. & Hariot, a discomycetous genus of critical taxonomic position. Sydowia 38:106–113
Gaumann EA (1949) Die Pilze, Grundzu¨ge ihrer Entwicklungsgeschichte und Morphologie. Birkhä user, Basel
George M (1895) British fungus–flora. A classified text–book of mycology. G. Bell and Sons, London
Glienke C, Pereira OL, Stringari D, Fabris J, Kava-Cordeiro V, Galli-Terasawa L, Cunnington J, Shivas RG, Groenewald JZ, Crous PW (2011) Endophytic and pathogenic Phyllosticta species, with reference to those associated with Citrus Black Spot. Persoonia 26:47–56
Goebel F, Kunze G (1827) Pharmazeutische Waarenkunde. Eisenach Gonidien. Österreichische botanische Zeitschrift 40:323–328
Gordon CC, Shaw CG (1960) A new genus of the Meliolaceae on the roots of Solanum species. Mycologia 52:331
Goree H (1974) Glyphium in western Canada and United States. Can J Bot 52:1265–1269
Gray SF (1821) A natural arrangment of British plants vol.1, p 519
Greville RK (1824) Flora Edinensis: or a description of plants growing near Edinburgh, arranged according to the linnean system. i–lxxxi, 4 tabs. Blackwood, Edinburgh, p 478
Greville RK (1825a) Scottish cryptogamic flora or coloured figures and descriptions of cryptogamic plants found in Scotland and belonging chiefly to the order fungi and intended to serve as a continuation of english botany 3: tabs. Maclachnan, Edinburgh, pp 121–180
Greville RK (1825b, publ. 1826) Scottish Cryptogamic Flora 4 (37–48): plates 181–240. Scotland, Edinburgh
Griffiths D (1901) The North American Sordariaceae. Mem Torrey Bot Club 11:1–134
Groenewald JZ, Nakashima C, Nishikawa J, Shin HD, Park JH, Jama AN, Groenewald M, Braun U, Crous PW (2012) Species concepts in Cercospora: spotting the weeds among the roses. Stud Mycol 75:115–170
Groenewald JZ, Nakashima C, Nishikawa J, Shin HD, Park JH, Jama AN, Groenewald M, Braun U, Crous PW (2013) Species concepts in Cercospora: spotting the weeds among the roses. Stud Mycol 75:115–170
Groenhart P (1951) Malaysian lichens III. Cyanoporina Groenh., an interesting lichen from Java. Reinwardtia 1:197–198
Grube M (1993) Über metachromatisches Färbeverhalten bei einigen Arten der Sammelgattung Arthopyrenia, mit weiteren Beispielen aus ähnlichen Gattungen (Ascomycetes, Arthopyreniaceae). Nova Hedwigia 57:473–482
Hafellner J (1979) Kurschia. Revision einer Sammelgattung an der Grenze von lichenisierten und nichtlichenisierten Ascomyceten. Beih Nova Hedwigia 62:1–248
Hafellner J (1982) Studien uber lichenicole Pilze und Flechten II. Lichenostigma maureri gen. et spec. nov., ein in den Ostalpen haufiger lichenicoler Pilz (Ascomycetes, Arthoniales). Herzogia 6:299–308
Halici MG, Hawksworth DL (2008) Two new species of Dacampia (Ascomycota, Dacampiaceae), with a key to and synopsis of the known species of the genus. Fungal Divers 28:49–54
Hall T (2004) BioEdit v. 7.0.1. Department of Microbiology, North Carolina State University. Available at www.mbio.ncsu.edu/BioEdit/bioedit.html
Hambleton S, Egger KN, Currah RS (1998) The genus Oidiodendron: species delimitation and phylogenetic relationship based on nuclear ribosomal DNA analysis. Mycologia 90:854–869
Hambleton S, Tsuneda A, Currah RS (2003) Comparative morphology and phylogenetic placement of two microsclerotial black fungi from Sphagnum. Mycologia 95:959–975
Hanlin RT (1989) Illustrated genera of ascomycetes. APS Press. The American Phytopathological Society, St. Paul
Hansford GC (1945) Contributions towards the fungus flora of Uganda. VII. New records and revisions. Proc Linnean Soc London 157:37–38
Hansford GC (1946) The foliicolous ascomycetes, their parasites and associated fungi. Mycol Pap 15:1–240
Harris RC (1973) The corticoloios pyrenolichens of the Great Lakes region. Mich Bot 12:3–68
Harris RC (1975) A taxonomic revision of the genus Arthopyrenia Massal. s. lat. (Ascomycetes) in North America. Ph.D. Thesis, Michigan State University, USA, p 288
Harris R (1984) The family Trypetheliaceae (Loculoascomycetes: lichenized Melanommatales) in Amazonian Brazil. Suppl Acta Amazônica 14:55–80
Harris RC (1990) Some Florida lichens. Publ. by the Author, Bronx
Harris RC (1995) More Florida lichens. Including the 10c tour of the pyrenolichens. Author, Bronx
Hatakeyama S, Tanaka K, Harada Y (2005) Bambusicolous fungi in Japan (5): three species of Tetraploa. Mycoscience 46:196–200
Hausmann S, Lotter AF, van Leeuwen JFN, Ohlendorf C, Lemcke G, Grönlund R, Sturm M (2002) Interactions of climate and land use documented in the varved sediments of Seebergsee in the Swiss Alps. Holocene 12:279–289
Hawksworth DL (1977) Taxonomic and biological observations on the genus Lichenoconium (Sphaeropsidales). Persoonia 9:159–198
Hawksworth DL (1979) Ascospore sculpturing and generic concepts in the Testudinaceae (syn. Zopfiaceae). Can J Bot 57:91–99
Hawksworth DL (1981) Lichenothelia, a new genus for the Microthelia aterrima group. Lichenologist 13:141–153
Hawksworth DL (1985a) A redisposition of the species referred to the ascomycete genus Microthelia. Bulletin of the British Museum (Natural History). Botany 14:43–181
Hawksworth DL (1985b) Kirschsteiniothelia a new genus for the Microthelia incrustans–group (Dothideales). Bot J Linn Soc 91:181–202
Hawksworth DL (2012) Managing and coping with names of pleomorphic fungi in a period of transition. Mycosphere 3:143–155
Hawksworth DL, Boise JR (1985, publ. 1986) Some additional species of Astrosphaeriella, with a key to the members of the genus. Sydowia 38:114–124
Hawksworth DL, Booth C (1974) A revision of the genus Zopfia Rabenh. Mycol Pap 135:1–38
Hawksworth DL, David JC (1989) Proposals for nomina conservanda and rejicienda for ascomycete names (lichenized and nonlichenized). Taxon 38:493–499
Hawksworth DL, Diederich P (1988) A synopsis of the genus Polycoccum (Dothideales), with a key to accepted species. Trans Br Mycol Soc 90:293–312
Hawksworth DL, Eriksson OE (1986) The names of accepted orders of ascomycetes. Syst Ascomycetum 5:175–184
Hawksworth DL, Eriksson OE (1988) Proposals to conserve 11 family names in the Ascomycotina (Fungi). Taxon 37:190–193
Hawksworth DL, Mcmanus PM (1989) Lichen recolonization in London under conditions of rapidly falling sulphur dioxide levels, and the concept of zone skipping. Bot J Linn Soc 100:99–109
Hawksworth DL, Kirk PM, Sutton BC, Pegler DN (1983) Ainsworth & Bisby’s dictionary of the fungi. Commonwealth Mycological Institute, Kew
Hawksworth DL, Kirk PM, Sutton BC, Pegler DN (1995) Ainsworth & Bisby’s dictionary of the fungi, 8th edn. CAB International, Wallingford
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
Hedrick J (1942) Some lichens from the American tropics collected by Wm. R. Taylor. Allan Hancock Pac Expeditions 3:183–187
Hennings PC (1895) Fungi Goyazenses. Hedwigia 34:88–116
Hennings PC (1900) Fungi japonica. Botanische Jahrbücher für Systematik, Pflanzengeschichte und Pflanzengeographie. Pflanzengeogr 28:259–280
Hennings PC (1904a) Einige neue Pilze aus Japan. Hedwigia 43:143–144
Hennings P (1904b) Fungi Africae orientalis III. Bot Jahrb Syst Pflanzengesch Pflanzengeogr 34:39–57
Hennings PC (1904c) Fungi fluminenses a cl. E. Ule collecti. Hedwigia 43:78–95
Henssen A (1964) Was it Pyrenothrix nigra? Ber Deut Bot Ges 77:317–322
Henssen A (1987) Lichenothelia, a genus of microfungi on rocks. In: Peveling E (ed) Progress and problems in lichenology in the eighties. Bibliotheca Lichenologica No.25. J. Cramer, Berlin-Stuttgart, pp 257–293
Henssen A (1995) Studies on the biology and structure of Dacampia (Dothideales), a genus with lichenized and lichenicolous species. Cryptogam Bot 5:149–158
Henssen A, Jahns HM (1973) Lichenes. Georg Thieme Verlag, Stuttgart
Henssen A, Thor G (1994) Developmental morphology of the ‘Zwischengruppe’ between Ascohymeniales and Ascoloculares. In: Hawksworth DL (ed) Ascomycete systematics. Problems and perspectives in the nineties. NATO ASI series vol 269. Plenum Press, New York and London, pp 43–56
Herrera-Campos ML, Huhndorf S, Lücking R (2005) The foliicolous lichen flora of Mexico IV: a new, foliicolous species of Pyrenothrix (Chaetothyriales, Pyrenothrichaceae). Mycologia 97:356–361
Hibbett DS, Binder M, Bischoff JF, Blackwell M, Cannon PF, Eriksson OE, Huhndorf S, James ST, Kirk PM, Lucking R, Lumbsch HT, Lutzoni F, Matheny PB, Mclaughlin DJ, Powell MJ, Redhed S, Schoch CL, Spatafora JF, Stalpers JA, Vilgalys R, Aime MC, Aptroot AA, Bauer R, Begerow D, Benny GL, Castelbury LA, Crous PW, Dai YC, Gams W, Geiser DM, Griffith GW, Gueidan C, Hawksworth DL, Hestmark G, Hosaka K, Humber RA, Hyde KD, Ironisde JE, Koljag U, Kurtzman CP, Larsson KH, Lichtwardt R, Longcore J, Miadlikowska J, Miller A, Moncalvo JM, Mozley-Standridge S, Oberwinkler F, Parmasto E, Reeb V, Rogers JD, Roux C, Ryvarden L, Sampaio JP, Schβler A, Sugiyama J, Thorn RG, Tibell L, Untereiner WA, Walker C, Wang Z, Weir A, Weiss M, White MM, Winka K, Yao YJ, Zhang N (2007) A higher–level phylogenetic classification of the fungi. Mycol Res 111:509–547
Hillis DM, Bull JJ (1993) An empirical test of bootstrapping as a method for assessing confidence in phylogenetic analysis. Syst Biol 42:182
Hino I, Katumoto K (1965) Notes on bambusicolous fungi (1). J Japanese Bot 40:81–89
Hirayama K, Tanaka K (2011) Taxonomic revision of Lophiostoma and Lophiotrema based on reevaluation of morphological characters and molecular analyses. Mycoscience 52:401–412
Hirayama K, Tanaka K, Raja HA, Miller AN, Shearer CA (2010) A molecular phylogenetic assessment of Massarina ingoldiana sensu lato. Mycologia 102:729–746
Hodhod MS, Abdel-Wahab MA, Bahkali AHA, Hyde KD (2012) Amarenographium solium sp nov from Yanbu mangroves in the Kingdom of Saudi Arabia. Cryptogam Mycol 33(3):285–294
Hofmann TA, Piepenbring M (2006) New records and host plants of fly–speck fungi from Panama. Fungal Divers 22:55–70
Hofmann TA, Kirschner R, Piepenbring M (2010) Phylogenetic relationships and new records of Asterinaceae (Dothideomycetes) from Panama. Fungal Divers 43:39–53
Höhn.ex Trotter, Sacc., D. Sacc. & Traverso [as ‘Schizothyrieae’] (1928) in Saccardo, Syll. fung. (Abellini) 24(2):1254
Hohnel FXR (1907) Eumycetes et myxomycetes. Denskriften der Kaiserlichen Akademie der Wissenschaften 1(118):813–904
Holm L, Holm K (1977) A study of Leptopeltidaceae. Bot Notiser 130:215–229
Holm L, Holm K (1988) Studies in the Lophiostmataceae with emphasis on the Swedish species. Symbolae Botanicae Upsalienses 28:1–50
Hooker JD (1847) The Botany of the Antarktic Voyage of H.M. Discovery Ships Erebus and Terror in the Years 1839-43 under the Command of Captain Sir James Clark Ross. I. Flora Antarctica Part 1.- London
Hooker JD, Harvey WH (1847) Algae Antarctiae: being characters and descriptions of the hitherto unpublished species of Algae, discovered in Lord Auckland’s Group, Campbell’s Islands, Kerguelen’s Land, Falkland Islands, Cape Horn and other southern circumpolar regions, during the voyage of H.M. discovery ships “Erebus” and “Terror”. London J Bot 4:249–276, 293–298
Hosagoudar VB (2003) Studies on Foliicoclous fungi–XIII a new genus and a new species. Zoos Print J 18:1159–1162
Hosagoudar VB (2004) Studies on Foliicolous fungi. Econ Taxon Bot 28:187–195
Hosagoudar VB (2006) Additions to the fungi of Kerala. Zoos’ Print J 21(8):2356–2371
Hosagoudar VB (2011) The genus Schiffnerula in India. Plant Pathol Quar 1:131–204
Hosagoudar VB (2012) Asterinales of India. Mycosphere 2(5):617–852
Hosagoudar VB (2013) My contribution to the fungal knowledge of India. J Threatened Taxa 5(8):4129–4348
Hosagoudar VB, Biju CK, Abraham TK (2004) Additions to Asterinaceae. Indian Phytopathol 57:114–116
Hosagoudar VB, Sabeena A, Kamarudeen M (2011a) A new species of the genus Englerula from India. Mycosphere 2:215–217
Hosagoudar VB, Thimmaiah C, Jayashankara M (2011b) Schiffnerulaceous fungi of Kodagu, Karnataka, India. J Threatened Taxa 3:2268–2271
Hu DM, Cai L, Chen H, Bahkali AH, Hyde KD (2010) Four new freshwater fungi associated with submerged wood from Southwest Asia. Sydowia 62:191–203
Huelsenbeck JP, Ronquist F (2001) MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 17:754–755
Hughes SJ (1953a) Conidiophores, conidia and classification. Can J Bot 31:577–659
Hughes SJ (1953b) Fungi from the Gold Coast. II. Mycol Pap 50:1–104
Hughes SJ (1965) New Zealand Fungi: 5. Trichothallus and Plokamidomyces states of Trichopeltheca. N Z J Bot 3:320–332
Hughes SJ (1966) New Zealand Fungi 7. Capnocybe and Capnophialophora, new form genera of sooty moulds. N Z J Bot 4:333–353
Hughes SJ (1968) Strigopodia. Can J Bot 46:1099–1107
Hughes SJ (1972) New Zealand fungi 17. Pleomorphism in Euantennariaceae and Metacapnodiaceae, two new families of sooty moulds. N Z J Bot 10:225–242
Hughes SJ (1974) New Zealand Fungi 22. Euantennaria with Antennatula and Hormisciomyces states. N Z J Bot 12(3):299–356
Hughes SJ (1976) Sooty moulds. Mycologia 68:693–820
Hughes SJ (1981) New Zealand Fungi 31. Capnobotrys, an anamorph of Metacapnodiaceae. N Z J Bot 19:193–226
Hughes SJ (1993) Meliolina and its excluded species. Mycol. Pap. 166:176
Hughes SJ (2000) Antennulariella batistae n.sp. and its Capnodendron and Antennariella synanamorphs with notes on Capnodium capsuliferum. Can J Bot 78:1215–1226
Hughes SJ (2003) Capnofrasera dendryphioides, a new genus and species of sooty moulds. N Z J Bot 41:139–146
Hughes SJ (2007) Heteroconium and Pirozynskiella n. gen., with comments on conidium transseptation. Mycologia 99:628–638
Hughes SJ, Seifert KA (2012) Taxonomic and nomenclatural notes on Sooty mould names based on species mixtures: Hormiscium handelii and Torula lechleriana. Mycoscience 53:17–24
Huhndorf SM (1992) Neotropical ascomycetes 2. Hypsostroma, a new genus from the Dominican Republic and Venezuela. Mycologia 84:750–758
Huhndorf SM (1994) Neotropical Ascomycetes 5. Hypsostromataceae, a new family of Loculoascomycetes and Manglicola samuelsii, a new species from Guyana. Mycologia 86:266–269
Huhndorf SM, Glawe DA (1990) Pycnidial development from ascospores of Fenestella princeps. Mycologia 82:541–548
Huhndorf SM, 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 Caribbean and elsewhere. Sydowia 55:172–180
Hyde KD (1988) Studies on the tropical marine fungi of Brunei. Bot J Linn Soc 98:135–151
Hyde KD (1991) A new amphisphaeriaceous fungus from intertidal fronds of Nypa fruticans. Trans Mycol Soc Jpn 32:265–271
Hyde KD (1992b) Tropical Australian freshwater fungi 1. Aust Syst Bot 6:161–167
Hyde KD (1992c) The genus Saccardoella from intertidal mangrove wood. Mycologia 84(5):803–810
Hyde KD (1992d) Julella avicenniae (Borse) comb. nov. (Thelenellaceae) from intertidal mangrove wood and miscellaneous fungi from the NE coast of Queensland. Mycol Res 96:939–942
Hyde KD (1995) The genus Massarina, with a description of M.eburnea and an annotated list of Massarina names. Mycol Res 99:291–296
Hyde KD (1996) Fungi from palms. XXIV. The genus Bondiella. Mycotaxon 57:347–352
Hyde KD (1997) The genus Roussoëlla, including two new species from palms in Cuyabeno, Ecuador. Mycol Res 101(5):609–616
Hyde KD, Borse BD (1986) Marine fungi from Seychelles V. Biatriospora marina gen. et sp. nov. from mangrove wood. Mycotaxon 26:263–270
Hyde KD, Borse BD (1991) Marine fungi from Seychelles VI. Massarina velatospora a new marine ascomycotina from mangrove wood. Mycotaxon 27:161–167
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
Hyde KD, Steinke TS (1996) Two new species of Delitschia from submerged wood. Mycoscience 37:99–102
Hyde KD, Eriksson OE, Yue J-Z (1996) Roussoëlla, an ascomycete genus of uncertain relationships with a Cytoplea anamorph. Mycol Res 100:1522–1528
Hyde KD, Aptroot A, Fröhlich J, Taylor JE (2000) Fungi from palms. XLIII. Lophiostoma and Astrosphaeriella species with slit–like ostioles. Nova Hedwigia 70:143–160
Hyde KD, McKenzie EHC, KoKo TW (2011) Towards incorporating anamorphic fungi in a natural classification checklist and notes for 2010. Mycosphere 2:1–88
Hyun JW, Timmer LW, Lee SC, Yun SH, Ko SW, Kim KS (2001) Pathological characterization and molecular analysis of Elsinoё isolates causing scab diseases of Citrus in Jeju Island in Korea. Plant Dis 85:1013–1017
Inácio CA, Cannon PF (2008) The genera of the Parmulariaceae. CBS biodiversity series vol 8. CBS Fungal Biodiversity Centre, Utrecht
Inácio CA, Araúz K, Piepenbring M (2012) A new genus of Parmulariaceae from Panama. Mycol Prog 11–6
Inderbitzin P, Landvik S, Abdel-Wahab MA, Barbee ML (2001) Aliquandostipitaceae, a new family for two new tropical ascomycetes with unusually wide hyphae and dimorphic ascomata. Am J Bot 88:52–61
Index Fungorum (2013) http://www.indexfungorum.org/Names/Names.asp, Accession Date −02 November 2012
Jaag O, Thomas E (1934) Neue Untersuchungenüber die Flechte Epigloeabactrospora Zukal. Ber Schweizerischen Botanischen Ges 43:77–89
Jackson S, Maxwell A, Neumeister-Kemp H, Dell B, Hardy G (2004) Infection, hyperparasitism and conidiogenesis of Mycosphaerella lateralis on Eucalyptus globulus in Western Australia. Australas Plant Pathol 33:49–53
Janex-Favre MC (1971) Recherches sur l’ontogenie, l’organisation et les asques de quelques pyrenolichens. Rev Bryol Lichenol 37:421–469
Jeng RS, Cain RF (1976) A new species of Eoterfezia from Mexico and Venezuela. Mycotaxon 3:387–390
Jenkins AE, Ukkelberg HG (1935) Scab of Golden rod caused by Elsinoё. J Agric Res 51:515–525
Jones EBG, Sakayaroj J, Suetrong S, Somrithipol S, Pang KL (2009a) Classification of marine Ascomycota, anamorphic taxa and Basidiomycota. Fungal Divers 35:1–187
Jones EBG, Sakayaroj J, Suetrong S, Somrithipol S, Pang KL (2009b) Classification of marine origin and evolution of fundamental reproductive and ecological traits. Syst Biol 58:224–239
Jones GE, Pang KL, Stanley SJ (2012) Fungi from marine algae. In: Jones EBG et al. (ed) Marine fungi and fungal-like organisms. Mar Freshw Botany 329–344
Kaiser WJ, Viruega JR, Peever TL, Trapero A (2008) First report of ascochyta blight outbreak of pea caused by Ascochyta pisi in Spain. Plant Dis 92:1365
Kalb K, Hafellner J, Staiger B (1995) Haematomma–Studien II. Lichenicole Pilze auf Arten der Flechtengattung Haematomma. Bibl Lich 59:199–222
Kang JC, Kong R, Hyde KD (1998) Studies on the Amphisphaeriales l. Amphisphaeriaceae (sensu stricto) and its phylogenetic relationships inferred from 5.8S rDNAand ITS2 sequences. Fungal Divers 1:147–157
Kang HJ, Sigler L, Lee J, Gibas CFC, Yun SH, Lee YW (2010) Xylogone ganodermophthora sp. nov., an ascomycetous pathogen causing yellow rot on cultivated mushroom Ganoderma lucidum in Korea. Mycologia 102:1167–1184
Kantvilas G, Coppins BJ (1997) Melaspilea circumserpens Nyl. rediscovered and referred to Glonium, with discussion on the provenance of some of Robert Brown’s lichen specimens. Lichenologist 29:525–531
Kar AK, Maity MK (1971) Leaf–inhabiting pyrenomycetes of West Bengal (India). Mycologia 63:1024–1029
Karsten PA (1887) Symbolae ad Mycologiam Fennicam. Pars XXI. Meddn Soc Fauna Flora fenn 14:103–110
Kashiwadani H, Aptroot A, Moon KH (2009) New pyrenocarpous lichens in Japan, with the resurrection of the genus Trypetheliopsis for Musaespora. Bibl Lichenologica 99:247–258
Kendrick B, DiCosmo F (1979) Teleomorph–anamorph connections in ascomycetes. In: Kendrick B (ed) The whole fungus. National Museums of Canada, Ottawa, pp 283–410
Khan JA, Hussain ST, Hasan S, McEvoy P, Sarwari A (2000) Disseminated bipolaris infection in an immunocompetent host: an atypical presentation. J Pak Med Assoc 50:68–71
Khashnobish A, Shearer CA (1996) Phylogenetic relationships in some Leptosphaeria and Phaeosphaeria species. Mycol Res 100:1355–1363
Kirchmair M, Neuhauser S, Buzina W, Huber L (2008) The taxonomic position of Roesleria subterranea. Mycol Res 112:1210–1219
Kirk PM, Cannon PF, David JC, Stalpers JA (2001) Ainsworth & Bisby’s dictionary of the fungi, 9th edn. CABI, Wallingford
Kirk PM, Cannon PF, Minter DW, Stalpers JA (2008) Ainsworth & Bisby’s dictionary of the fungi, 10th edn. CABI, Wallingford
Kirschner R, Araúz V, Herbst F, Hofmann TA, Ix S, Nozon T, Piepenbring M (2010) A new species of Puttemansia (Pleosporales) and new records of further Ascomycota from Panama. Sydowia 62:225–241
Kirschstein W (1911) Sphaeriales. Kryptogamen–Flora der Mark Brandenburg 7:164–304
Kirschstein W (1924) Beitra¨ge zur Kenntnis der Ascomyceten. Verhandlungen des Botanischen Vereins der Provinz Brandenburg 66:23–29
Kishi K (1998) Plant diseases in Japan. Zenkoku Noson Kyoiku Kyokai, Tokyo, p 1128
Knudsen K, Lendemer JC (2009) Naetrocymbe herrei (Pleosporales; Ascomycetes), a new lichenized saxicolous species from the coast of central California. Opuscula Philolichenum 6:59–64
Kobayashi T, Katsumoto K, Abiko K, Abe Y, Kakishima M (1992) Illustrated genera of plant pathogenic fungi in Japan. Zenkoku Noson Kyoiku Kyokai, Tokyo, p 200
Kocourková J, Knudsen K (2009) A new species of Stigmidium (Mycosphaerellaceae, Ascomycetes) from western North America. Czech Mycol 61:73–80
Kodsueb R, Dhanasekaran V, Aptroot A, Lumyong S, McKenzie EHC, Hyde KD, Jeewon R (2006a) The family Pleosporaceae: intergeneric relationships and phylogenetic perspectives based on sequence analyses of partial 28S rDNA. Mycologia 98:571–583
Kodsueb R, Jeewon R, Vijaykrishna D, Mckenzie EHC, Lumyong P, Lumyong S, Hyde KD (2006b) Systematic revision of Tubeufiaceae based on morphological and molecular data. Fungal Divers 21:105–130
Kodsueb R, Lumyong S, Ho WH, Hyde KD, McKenzie EHC, Jeewon R (2007) Morphological and molecular characterization of Aquaticheirospora and phylogenetics of Massarinaceae (Pleosporales). Bot J Linn Soc 155:283–296
Kohlmeyer J (1963) Zwei neue Ascomyceten gattungen auf Posidonia rhizomen. Nova Hedwigia 6:5–13
Kohlmeyer J (1986) Ascocratera manglicola gen. et sp. nov. and key to the marine Loculoascomycetes on mangroves. Can J Bot 64:3036–3042
Kohlmeyer J, Kohlmeyer E (1971) Marine fungi from tropical America and Africa. Mycologia 63:831–861
Kohlmeyer J, Kohlmeyer B (1979) Marine fungi: the higher fungi. Academic, New York
Kohlmeyer J, Schatz S (1985) Aigialus gen. nov. (Ascomycetes) with two new marine species from mangroves. Trans Br Mycol Soc 85:699–707
Kohlmeyer J, Volkmann-Kohlmeyer B (1990) Revision of marine species of Didymosphaeria (Ascomycotina). Mycol Res 94:685–690
Kohlmeyer J, Volkmann-Kohlmeyer B (1998a) A new marine Xylomyces on Rhizophora from the Caribbean and Hawaii. Fungal Divers 1:159–164
Kohlmeyer J, Volkmann-Kohlmeyer B (1998b) Mycophycias, a new genus for the mycobionts of Apophlaea, Ascophyllum and Pelvetia. Syst Ascomycetum 16:1–7
Kohlmeyer J, Volkmann-Kohlmeyer B, Eriksson OE (1995a) Fungi on Juncus roemerianus. New marine and terrestrial ascomycetes. Mycol Res 100:393–401
Kohlmeyer J, Volkmann-Kohlmeyer B, Eriksson OE (1995b) Fungi on Juncus roemerianus 2. New dictyosporus ascomycetes. Bot Mar 38:165–174
Kohlmeyer J, Hawksworth DL, Volkmann-Kohlmeyer B (2004) Observations on two marine and maritime “borderline” lichens: Mastodia tessellata and Collemopsidium pelvetiae. Mycol Prog 351–356
Körber GW (1865) Ergänzungen zum Systema lichenum Germaniae. Parerga lichenologica. (Breslau) pp 385–501
Kruys A, Wedin M (2009) Phylogenetic relationships and an assessment of traditionally used taxonomic characters in the Sporormiaceae (Pleosporales, Dothideomycetes, Ascomycota), utilising multigene phylogenies. Syst Biodivers 7:465–478
Kruys A, Eriksson OE, Wedin M (2006) Phylogenetic relationships of coprophilous Pleosporales (Dothideomycetes, Ascomycota), and the classification of some bitunicate taxa of unknown position. Mycol Res 110:527–536
Kutorga E, Hawksworth DL (1997) A reassessment of the genera referred to the family Patellariaceae (Ascomycota). Syst Ascomycetum 15:1–110
Larget B, Simon DL (1999) Markov chain Monte Carlo algorithms for the Bayesian analysis of phylogenetic trees. Mol Biol Evol 16:750–759
Larone DH (1995) Medically important fungi. A guide to identification, 3rd edn. ASM Press, Washington
Lawrey JD, Diederich P, Nelsen MP, Sikaroodi M, Gillevet PM, Brand AM, van den Boom P (2011) The obligately lichenicolous genus Lichenoconium represents a novel lineage in the Dothideomycetes. Fungal Biol 115:176–187
Lawrey JD, Diederich P, Nelsen MP, Freebury C, Broeck DVD, Sikaroodi M, Ertz D (2012) Phylogenetic placement of lichenicolous Phoma species in the Phaeosphaeriaceae (Pleosporales, Dothideomycetes). Fungal Divers 55:195–213
Letrouit-Galinou MA, Parguey-Leduc A, Janex-Favre MC (1994) Ascoma structure and ontogenesis in ascomycete systematics. In: Hawksworth DL (ed) Ascomycete systematics. Problems and perspectives in the nineties. NATO ASI, vol 269. Plenum Press, New York and London, pp 23–36
Leuchtmann A (1985a) Kulturversuche mit einigen Arten der Gattung Lophiostoma Ces. & De Not. Sydowia 38:158–170
Leuchtmann A (1985b) Über Phaeosphaeria Miyake und andere bitunicate Ascomyceten mit mehrfach querseptierten ascosporen. Sydowia 37:75–194
Li YM, Haixia Wu, Cheng H, Hyde KD (2011) Morphological studies in Doithideomycetes: Elsinoё (Elsinoaceae), Butleria and three excluded genera. 115:507–520
Li H, Sun G, Zhai X, Batzer J, Mayfield D, Crous P, Groenewald J, Gleason M (2012) Dissoconiaceae associated with sooty blotch and flyspeck on fruits in China and the United States. Persoonia 28:113–125
Libert MA (1834) Plantae Cryptogamae, quas in Arduenna collegit. Fasc. 3:no. 272
Liew ECY, Aptroot A, Hyde KD (2000) Phylogenetic significance of the pseudoparaphyses in Loculoascomycete taxonomy. Mol Phylogenet Evol 16:392–402
Liew ECY, Aptroot A, Hyde KD (2002) An evaluation of the monophyly of Massarina based on ribosomal DNA sequences. Mycologia 94:803–813
Lindau G (1896) Hysteriineae. In: Engler & Prantl, Naturliche Pflanzenfamilien. I. Teil, I. Abteilung 1:265–278
Lindau G (1897) Pyrenomycetineae, Laboulbeniineae. Engler Prantl Nat Pflanzenfamilien Teil I (Leipzig) 1:321–505
Lindemuth R, Wirtz N, Lumbsch HT (2001) Phylogenetic analysis of nuclear and mitochondrial DNA sequences supports the view that loculoascomycetes (Ascomycota) are not monophyletic. Mycol Res 105:1176–1181
Link HF (1816) Observationes in ordines plantarum naturales. Mag Ges Naturf Fr Berl 2. 8:25–45
Liu D (2011) Piedraiain molecular detection of human fungal pathogens. CPC press. p 958
Liu YJ, Hall DB (2004) Body plan evolution of ascomycetes, as inferred from an RNA polymerase II Phylogeny. Proc Natl Acad Sci 101:4507–4512
Liu JK, Chomnunti P, Cai L, Phookamsak R, Chukeatirote E, Jones EBG, Moslem M, Hyde KD (2010) Phylogeny and morphology of Neodeightonia palmicola sp. nov. from palms. Sydowia 62:261–276
Liu JK, Phookamsak R, Jones EBG, Zhang Y, Ko-Ko TW, Hu HL, Boonmee S, Doilom M, Chukeatirote E, Bahkali AH, Wang Y, Hyde KD (2011) Astrosphaeriella is polyphyletic, with species in Fissuroma gen. nov., and Neoastrosphaeriella gen. nov. Fungal Divers 51:135–154
Liu JK, Phookamsak R, Doilom M, Wiki S, Mei LY, Ariyawansa HA, Boonmee S, Chomnunti P, Dai DQ, Bhat DJ, Romero AI, Xhuang WY, Monkai J, Jones EBG, Chukeatirote E, KoKo TW, Zhoa YC, Wang Y, Hyde KD (2012a) Towards a natural classification of Botryosphaeriales. Fungal Divers 57:149–210
Liu Y, Liu Z, Wongkaew S (2012b) Developing characteristics and relationships of Shiraia bambusicoloa with bamboo. Songklanakarin J Sci Technol 43:17–22
Liu YX, Hyde KD, Ariyawansa HA, Li WJ, Zhou DQ, Yang YL, Chen YM, Liu ZY (2013) Shiraiaceae, new family of Pleosporales (Dothideomycetes, Ascomycota). Phytotaxa 103:51–60
LoBuglio KF, Berbee ML, Taylor JW (1996) Phylogenetic origins of the asexual mycorrhizal symbiont Cenococcum geophilum Fr. and other mycorrhizal fungi among the ascomycetes. Mol Phylogenet Evol 6:287–294
Lohman ML (1932b) Three new species of Mytilidion in the proposed subgenus Lophiopsis. Mycologia 24:477–484
Lohman ML (1933a) Hysteriaceae: Life histories of certain species. Pap Mich Acad Sci Arts Lett 17:229–288
Lohman ML (1933b) Septonema toruloideum: a stage of Mytilidion scolecosporum. Mycologia 25:34–43
Lohman ML (1934) A cultural and taxonomic study of Hysterium hyalinum. Pap Mich Acad Sci Arts Lett 19:133–140
Loquin MV (1974) Réorganisation de la systematique des champignons selon les donneés de revolution heliocyclique. Bulletin Mensuel de la Société Linnéenne de Lyon 43, num. spéc. 43:233–238
Lorenzo LE, Messuti MI (2005) Glyphium elatum (Ascomycota) in Patagonia (Argentina). Boletin Soc Argent Bot 40:13–16
Luck-Allen ER, Cain RF (1975) Additions to the genus Delitschia. Can J Bot 53:1827–1887
Lücking R (2008) Foliicolous lichenized fungi. Flora Neotropica Monogr 103:1–866
Lücking R, Sérusiaux E (1996) Musaespora kalbii (lichenized Ascomycetes: Melanommatales), a new foliicolous lichen with a pantropical distribution. Nord J Bot 16:661–667
Lücking R, Aptroot A, Thor G (1997) New species or interesting records of foliicolous lichens. II. Flavobathelium epiphyllum (lichenized Ascomycetes: Melanommatales). Lichenologist 29:221–228
Lücking R, Sérusiaux E, Maia LC, Pereira CG (1998) A revision of the names of foliicolous lichenized fungi published by Batista and co–workers between 1960 and 1975. Lichenologist 30:121–191
Lücking R, Sipman HJM, Umaña L, Chaves JL, Lumbsch HT (2007) Aptrootia (Dothideomycetes: Trypetheliaceae), a new genus of pyrenocarpous lichens for Thelenella terricola. Lichenologist 39:187–193
Lücking R, Seavey F, Common RS, Beeching SQ, Breuss O, Buck WR, Crane L, Hodges M, Hodkinson BP, Lay E, Lendemer JC, McMullin RT, Mercado-Díaz JA, Nelsen MP, Rivas Plata E, Safranek W, Sanders WB, Schaefer HP Jr, Seavey J (2011) The lichens of Fakahatchee Strand Preserve State Park, Florida: Proceedings from the 18th Tuckerman Workshop. Bull Florida Museum Nat Hist 49:127–186
Lumbsch HT (1999) The ascomata development in Mycoporum elabens (Mycoporaceae, Dothidiales). Plant Biol 1:321–326
Lumbsch HT, Huhndorf S (2007) Outline of Ascomycota. Myconet 13:1–99
Lumbsch HT, Huhndorf SM (2010) Myconet Volume 14. Part one. Outline of Ascomycota 2009. Part Two. Notes on Ascomycete Systematics. Nos. 4751–5113. Fieldiana Life Earth Sci 1:1–64
Lumbsch HT, Schmitt I, Lindemuth R, Miller A, Mangold A, Fernandez F, Huhndorf S (2005) Performance of four ribosomal DNA regions to infer higher–level phylogenetic relationships of inoperculate euascomycetes (Leotiomyceta). Mol Phylogenet Evol 34:512–524
Lundqvist N (1964) The genus Trichodelitschia in Sweden. Sven Bot Tidskr 58:267–272
Luttrell ES (1951) Taxonomy of Pyrenomycetes. Univ Missouri Stud 24(3):1–120
Luttrell ES (1955) The ascostromatic Ascomycetes. Mycologia 47:511–532
Luttrell ES (1973) Loculoascomycetes. In: Ainsworth GC, Sparrow FK, Sussman AS (eds) The fungi, an advanced treatise, a taxonomic review with keys: ascomycetes and fungi imperfecti. Academic, London, pp 135–219
Lutzoni F, Kauff F, Cox CJ, McLaughlin D, Celio G, Dentinger B, Padamsee M, Hibbett D, James TY, Baloch E, Grube M, Reeb V, Hofstetter V, Schoch CL, Arnold AE, Miadlikowska J, Spatafora J, Johnson D, Hambleton S, Crockett M, Shoemaker R, Sung GH, Lücking R, Lumbsch T, O’Donnell K, Binder M, Diederich P, Ertz D, Gueidan C, Hansen K, Harris RC, Hosaka K, Lim YW, Matheny B, Nishida H, Pfister D, Rogers J, Rossman AY, Schmitt I, Sipman H, Stone J, Sugiyama J, Yahr R, Vilgalys R (2004) Assembling the fungal tree of life: progress, classification, and evolution of subcellular traits. Am J Bot 91:1446–1480
Ma Y, Zhang R, Sun G, Zhu H, Tang M, Batzer JC, Gleason ML (2010) A new species of Zygophiala associated with the flyspeck complex on apple from China. Mycol Prog 9:151–155
Malathrakis NE (1979) A study of an olive tree disease caused by the fungus Phoma incompta Sacc. et Mart. Dissertation, Agricultural College of Athens
Malloch D (1970) The genera of cleistothecial Ascomycota. Ph.D. Thesis. University of Toronto
Malloch D (1981) The plectomycete centrum. In: Reynolds DR (ed) Ascomycete systematics. The Luttrellian concept. Springer–Verlag, New York, pp 73–91
Malloch D, Cain R (1971) Four new genera of cleistothecial ascomycetes with hyaline ascospores. Can J Bot 49:847–854
Malloch D, Cain RF (1972) New species and combinations of cleistothecial ascomycetes. Can J Bot 50:61–72
Malloch D, Sigler L (1988) The Eremomycetaceae (Ascomycotina). Can J Bot 66:1929–1932
Manamgoda DS, Cai L, McKenzie EHC, Crous PW, Madrid H, Chukeatirote E, Shivas RG, Tan YP, Hyde KD (2012) A phylogenetic and taxonomic re–evaluation of the Bipolaris, Cochliobolus, Curvularia Complex. Fungal Divers 56:131–144
Mangin L, Patouillard N (1913) Les Atichiales, groupe aberrant d’ascomycètes inférieurs. C R Hebdomadaires Seances Acad Sci Paris 154:1475–1481
Martin GW (1941) Outline of the Fungi. Studies in Natural History; Iowa University 18:1–64
Massalongo AB (1852) Ricerche sull’autonomia dei licheni crostosi e materiali pella loro naturale ordinazione. Frizerio, Verona
Massee G (1895) British fungus flora, a classified textbook of mycology 4:538. George Bell & Sons, London
Mathiassen G (1989) Some corticolous and lignicolous Pyrenomycetes s. lat. (Ascomycetes) on Salix in Troms, N Norway. Sommerfeltia 9:1–100
McCarthy PM (1995) New saxicolous species of Strigula Fr. (lichenised Ascomycotina: Strigulaceae) from Australia and New Zealand. Muelleria 8:323–329
McCarthy PM (1997) New and interesting saxicolous species of Strigula. Lichenologist 29:513–523
McCarthy PM (2001) The lichen genus Strigula in Christmas Island, Indian Ocean. Bibl Lichenologica 78:275–287
McCarthy PM (2009) Strigulaceae. Flora Aust 57:570–584, 593–601
McNeill J, Turland NJ, Monro AM, Lepschi BJ (2011) XVIII International Botanical Congress: preliminary mail vote and report of Congress action on nomenclature proposals. Taxon 60:1507–1520
Meeker JA (1975) Revision of the Seuratiaceae I. Morphology of Seuratia. Can J Bot 53:2462–2482
Messuti MI, Lorenzo LE (1997) A new species of Hysterium from Patagonia, Argentina. Mycol Res 101:302–304
Mibey RK, Hawksworth D (1995) Diporothecaceae, a new family of ascomycetes, and the term ‘hyphopodium’. Syst Ascomycetum 14:25–31
Miller JH (1928) Biologic studies in the Sphaeriales 1. Mycologia 20:187–213
Miller JH (1938) Studies in the development of two Myriangium species and the systematic position of the order Myriangiales. Mycologia 30:158–181
Miller JH (1949) A revision of the classification of the Ascomycetes with special emphasis on the Pyrenomycetes. Mycologia 41:99–127
Miller JH, Burton MG (1943) Studies in some Venezuelan ascomycetes collected by Chardon CE and Muller AS. Mycologia 35:83–94
Miller MA, Pfeiffer W, Schwartz T (2010) Creating the CIPRES Science Gateway for inference of large phylogenetic trees. In: Proceedings of the Gateway Computing Environments Workshop (GCE). San Diego Supercomput. Center, New Orleans, LA. CA pp 1–8
Minnis AM, Kennedy AH, Grenier DB, Rehner SA, Bischoff JF (2011) Asperisporium and Pantospora (Mycosphaerellaceae): epitypifications and phylogenetic placement. Persoonia 27:1–8
Minnis AM, Kennedy AH, Grenier DB, Palm ME, Rossman AY (2012) Phylogeny and taxonomic revision of the Planistromellaceae including its coelomycetous anamorphs: contributions towardsa monograph of the genus Kellermania. Persoonia 29:11–28
Minter DW, Peredo HL, Watson A (2007) Acrospermum chilense sp. nov. from Chile and the Acrospermales ord. nov. Bol Soc Argent Bot 42:107–112
Miyake I (1909) Studies on the parasitic fungi of rice in Japan. Bot Mag Tokyo 23:85–97
Monkai J, Liu JK, Boonmee S, Chomnunti P, Chukeatirote E, Jones EBG, Wang Y, Hyde KD (2013) Planistromellaceae (Botryosphaeriales). Cryptogam Mycol 34:45–77
Montagne JPFC (1842) Botanique. Plantes cellulaires. In: de la Sagra R (ed) Histoire Physique Politique et Naturelle de l’Ile de Cuba 2:1–549, France
Morakotkarn D, Kawasaki H, Tanaka K, Okane I, Seki T (2008) Taxonomic characterization of Shiraia–like fungi isolated from bamboos in Japan. Mycoscience 49:258–265
Moreau C (1953) Les genres Sordaria et Pleurage. Encyclopédie Mycol 25:1–130
Mugambi GK, Huhndorf SM (2009a) Molecular phylogenetics of Pleosporales: Melanommataceae and Lophiostomataceae recircumscribed (Plesporomycetidae, Dothideomycetes, Ascomycota). Stud Mycol 64:103–121
Mugambi GK, Huhndorf SM (2009b) Parallel evolution of hysterothecial ascomata in ascolocularous fungi (Ascomycota, Fungi). Syst Biodivers 7:453–464
Muggia L, Gueidan C, Knudsen K, Perlmutter G, Grube M (2012) The lichen connections of black fungi. Mycopathologia
Müller E (1950) Die schweizerischen Arten der Gattung Leptosphaeria und ihrer Verwandten. Sydowia 4:185–319
Müller E, Sanwal BD (1954) Über die Gattungen Microcyclus Sacc., Coccoidella v. Höhn., Coccodothis Theiss. et Syd. und Coccodothella Theiss. et Syd. Sydowia 8:231–244
Müller E, von Arx JA (1950) Einige Aspeckte zur Systematik pseudospharialer Ascomyceten. Ber Schweizerischen Botanischen Ges 60:329–397
Müller E, von Arx JA (1962) Die Gattungen der didymosporen Pyrenomyceten. Beitr Kryptogamenflora Schweiz 11(2):1–922
Müller E, von Arx JA (1973) Pyrenomycetes: Meliolales, Coronophorales, Sphaeriales. New exotic fungi. Grevillea 17(1888):42–43
Munk A (1953) The system of the pyrenomycetes. A contribution to a natural classification of the group Sphaeriales sensu Lindau. Dansk Botanisk Arkiv 15:1–163
Munk A (1956) On Metasphaeria coccodes (Karst.) Sacc. (Massarinaceae n. fam.). Friesia 5:303–308
Munk A (1957) Danish pyrenomycetes. A preliminary flora. Dansk Botanisk Arkiv 17:1–491
Muthumeenakshi S, Goldstein AL, Stewart A, Whipps JM (2001) Molecular studies on intraspecific diversity and phylogenetic position of Coniothyrium minitans. Mycol Res 105:1065–1074
MycoBank (2013) http://www.mycobank.org/BioloMICS.aspx?Link=T&TableKey=14682616000000061&Rec=44996&Fields=All
Nagasawa E, Otani Y (1977) Some species of the bambusicolous ascomycetes from Japan I. Rep Tottori Mycol Instit 15:38–42
Nakagiri A (1984) Two new species of Lulworthia and evaluation of genera–delimiting characters between Lulworthia and Lindra (Halosphaeriaceae). Trans Mycol Soc Jpn 25:377–388
Nannfeldt JA (1932) Studien uber die Morphologie und Systematik der nicht–lichenisierten, inoperkulaten Discomyceten. Nova Acta Regiae Soc Sci Uppsaliensis IV 8:1–368
Navarro-Rosinés P, Hafellner J (1996) Lichenostigma elongata spec. nov. (Dothideales), a lichenicolous ascomycete on Lobothallia and Aspicilia species. Mycotaxon 57:211–225
Nelsen MP, Lücking R, Grube M, Mbatchou JS, Muggia L, Rivas-Plata E, Lumbsch HT (2009) Unravelling the phylogenetic relationships of lichenised fungi in Dothideomyceta. Stud Mycol 64:135–144
Nelsen MP, Lücking R, Mbatchou JS, Andrew CJ, Spielmann AA, Lumbsch HT (2011a) New insights into relationships of lichen–forming Dothideomycetes. Fungal Divers 51:155–162
Nelsen MP, Rivas Plata E, Andrew CJ, Lücking R, Lumbsch HT (2011b) Phylogenetic diversity of trentepohlialean algae associated with lichen–forming fungi. J Phycol 47:282–290
Nelsen MP, Lücking R, Aptroot A, Cáceres MES, Lumbsch HT (2013) Attaining the phylogenetic disposition of Aspidotheliacea (Ascomycota), an orphaned family of lichen–forming fungi. In prep
Nelson S (2008) Citrus scab. Plant Dis 60:1–6
Nelson PE, Wilhelm S (1956) An undescribed fungus causing a root rot of strawberry. Mycologia 48:547–551
Nitschke TRJ (1869) Grundlage eines Systems der Pyrenomyceten. Verhandlungen des Naturhistorischen Vereins der Preussischen Rheinlande, Westfalens und des Regierungsbezirks Osnabrück 26:70–77
Nylander W (1854) Essai d’une nouvelle classification des Lichens. Mém Soc Imp Sci Nat Cherbourg 2:5–16
Nylander JAA (2004) MrModeltest 2.0. Program distributed by the author. Evolutionary Biology Centre, Uppsala University
Olivier C, Berbee ML, Shoemaker RA, Loria R (2000) Molecular phylogenetic support from ribosomal DNA sequences for origin of Helminthosporium from Leptosphaeria–like loculoascomycete ancestors. Mycologia 92:736–746
Orange A (2009) Lichenicolous fungi on Ionaspis lacustris. Mycotaxon 81:265–280
Orton CR (1924) Studies in the morphology of the Ascomycetes I. The stroma and the compound fructification of the Dothideaceae and other groups. Mycologia 16:49–95
Padhye AA, Gutekunst RW, Smith DJ, Punithalingam E (1997) Maxillary sinusitis caused by Pleurophomopsis lignicola. J Clin Microbiol 35(8):2136
Page RDM (1996) TreeView: an application to display phylogenetic trees on personal computers. Comput Appl Biosci 12:357–358
Pang KL, Abdel-Wahab MA, Sivichai S, El-Sharouney H, Jones EBG (2002) Jahnulales (Dothideomycetes, Ascomycota): a new order of lignicolous freshwater ascomycetes. Mycol Res 106:1031–1042
Pang KL, Jheng JS, Jones EBG (2011) Marine mangrove fungi of Taiwan. National Taiwan Ocean University Press, Keelung, pp 1–131
Pang KL, Hyde KD, Alias SA, Suetrong S, Jones EBG (2013) Dyfrolomycetaceae, a new family in the Dothideomycetes, Ascomycota. Cryptogamie Mycologie
Peever TL, Barve MP, Stone LJ, Kaiser WJ (2007) Evolutionary relationships among Ascochyta species infecting wild and cultivated hosts in the legume tribes Cicereae and Vicieae. Mycologia 99:59–77
Penzig G, Saccardo PA (1898) Diagnoses fungorum novorum in insula Java collectorum. Ser. II. Malpighia 11:491–530
Pereira OL, Barreto RW (2003) Anhellia verruco–scopiformans sp. nov. (Myriangiales) associated with scaby brooms of Croton migrans in Brazil. Fungal Divers 12:155–159
Pérez CA, Wingfield MJ, Altier NA, Blanchette RA (2009) Mycosphaerellaceae and Teratosphaeriaceae associated with Eucalyptus leaf diseases and stem cankers in Uruguay. For Pathol 39:349–360
Pérez-Ortega S, Ríos Ade L, Crespo A, Sancho LG (2010) Symbiotic lifestyle and phylogenetic relationships of the bionts of Mastodia tessellata (ascomycota, incertae sedis). Am J Bot 97:738–752
Persoon CH (1800) Icones et description Fugorum-minus cognitorum 2: 27–67 Lispsiae
Persoon CH (1801) Synopsis Methodica Fungorum, Henrich Dieterich Publ. 706 pages. Gottingae
Petrak F (1923a) Mykologische Notizen VI. No. 226. Über die Gattung Glonium Müh. Ann Mycol 21:225–227
Petrak F (1923b) Mykologische Notizen VI. No. 284. Psiloglonium finkii nov. sp. Ann Mycol 21:308–309
Petrak F (1934) Mykologische Notizen. XII. Nos. 751–850. Ann Mycol 32:317–447
Petrak F (1947) Über die Leptopeltineen. Sydowia 1:232–247
Petrak F (1952) Ergebnisse einer Revision der Grundtypen verschiedener Gattungen der Askomyzeten und Fungi Imperfecti. III. Sydowia 6:336–343
Petrak F (1953) Die Gattung Blasdalea Sacc. et Syd. Sydowia 7:343
Petrak F (1962) Uber die Gattung Saccardoella Speg. Sydowia 15:233–236
Petrak F, Ciferri R (1932) Fungi Dominicani. II. Ann Mycol 30:149–353
Petrak F, Sydow H (1929) Kritisch–systematische Original untersuchungen über Pyrenomyzeten, Sphaeropsideen und Melanconieen: IV. Ann Mycol 27:87–115
Petrini O, Samuels GL, Müller E (1979) Holmiella sabina (de Not.) comb. nov. (syn. Eutryblidiella sabina) and its Cornicularia–like anamorph, an endophyte on Juniperus species. BerSchweizerischen Botanischen Ges 89:80–90
Phillips AJL, Alves A, Pennycook SR, Johnston PR, Ramaley A, Akulov A, Crous PW (2008) Resolving the phylogenetic and taxonomic status of dark–spored teleomorph genera in the Botryosphaeriaceae. Persoonia 21:29–55
Phongpaicht S, Tanaka K, Hairayama K, Jones EBG (2009) Molecular systematics of the marine Dothideomycetes. Stud Mycol 64:155–173
Pinokiyo A, Singh KP (2006) New species and new record of foliicolous lichenized fungi from Sikkim (India). Mycotaxon 97:57–60
Pinruan U, Jones EBG, Hyde KD (2002) Aquatic fungi from peat swamp palms: Jahnula appendiculata sp. nov. Sydowia 54:242–247
Pirozynski KA (1972) Microfungi of Tanzania. I. Miscellaneous fungi on oil palm. II. New hyphomycetes. Mycol Pap 12:1–64
Pirozynski KA (1974) Meliolina mollis and two hypersites in India. Kavaka 2:33–41
Pirozynski KA, Shoemaker R (1970) Some Asterinaceae and Meliolaceae on conifers in Canada. Can J Bot 48:1321–1328
Plemenitaš A, Vaupotič T, Lenassi M, Kogej T, Gunde-Cimerman N (2008) Adaptation of extremely halotolerant black yeast Hortaeawerneckii to increased osmolarity: a molecular perspective at a glance. Stud Mycol 61:67–75
Poelt J (1969) Bastimmungsschlüssel europäischer Flechten. Cramer, Lehre
Poelt J (1974) Classification. In: Ahmadjian V, Hale ME (eds) The lichens. New York Academic Press, p 599–632
Promputtha I, Miller AN (2010) Three new species of Acanthostigma (Tubeufiaceae, Pleosporales) from the Great Smoky Mountains National Park. Mycologia 102(3):574–587
Punithalingam E (1969) Studies on Sphaeropsidales in culture. Mycol Pap 119:1–24
Quaedvlieg W, Kema GHJ, Groenewald JZ, Verkley GJM, Seifbarghi S, Razavi M, Mirzadi Gohari A, Mehrabi R, Crous PW (2011) Zymoseptoria gen. nov.: a new genus to accommodate Septoria-like speciesoccurring on graminicolous hosts. Persoonia 26:57–69
Quaedvlieg W, Groenewald JZ, De Jesús Yáñez–Morales M, Crous PW (2012) DNA barcoding of Mycosphaerella species of quarantine importance to Europe. Persoonia 29:101–115
Quaedvlieg W, Verkley GJM, Shin H-D, Barretto RW, Alfenas AC, Swart WJ, Groenewald JZ, Crous PW (2013) Sizing up Septoria. Stud Mycol 75:307–390
Rabenhorst L (1863) Fungi Europaei Exsiccati. Editio novo. Century VI (nos 501–600). Dresden
Raciborski M (1900) Parasitische. Algen und Pilze Java’s. I. Theil. Staatsdruckerei. Batavia, p 39
Raja HA, Shearer CA (2006) Jahnula species from North and Central America, including three new species. Mycologia 98:312–332
Raja HA, Shearer CA (2008) Freshwater ascomycetes: new and noteworthy species from aquatic habitats in Florida. Mycologia 100:467–489
Raja HA, Schoch CL, Hustad V, Shearer C, Miller A (2011) Testing the phylogenetic utility of MCM7 in the Ascomycota. MycoKeys 1:63–94
Raja HA, Miller AN, Shearer CA (2012) Freshwater ascomycetes: Natipusillaceae, a new family of tropical fungi, including Natipusilla bellaspora sp. nov. from the Peruvian Amazon. Mycologia 104:569–573
Raja HA, Oberlies NH, Tamam-El Elimat, Miller AN, Zelski SE, Shearer CA (2013a) Lindgomyces angustiascus, (Lindgomycetaceae, Pleosporales, Dothideomycetes), a new lignicolous species from freshwater habitats in the USA. Mycoscience, in press
Raja HA, Tanaka K, Hirayama K, Hashimoto A, Oberlies NH, Figueroa M, Miller AN, Zelski SE, Shearer CA (2013b) Freshwater ascomycetes: Minutisphaera (Dothideomycetes) revisited, including one new species from Japan. Mycologia in press
Rajeshkumar KC, Sharma R (2013) Tamhinispora a new genus belongs to family Tubeufiaceae from the Western Ghats, India based on morphology and phylogenetic analysis. Mycosphere 4:165–174
Ramaley AW (1991) Fungi of Yucca baccata. 1. Piptarthron pluriloculare and its teleomorph, Planistroma yuccigena. Mycotaxon 42:63–75
Ramaley AW (1992) Fungi from Yucca baccata. 2. Planistroma obtusilunatum sp. nov. and its anamorph Piptarthron uniloculare sp. nov. Mycotaxon 45:449–460
Ramaley AW (1993) New fungi from Yucca: Planistromella yuccifoliorum, gen. et sp. nov. and its anamorph Kellermania yuccifoliorum, sp. nov. and Planistromella uniseptata sp. nov. the teleomorph of Kellermania yuccigena. Mycotaxon 47:259–274
Ramaley AW (1995) New species of Kellermania, Piptarthron, Planistroma, Planistromella from members of the Agavaceae. Mycotaxon 50:255–268
Ramaley AW (1998) New teleomorphs of the anamorphic genus Kellermania. Mycotaxon 66:509–514
Ramaley AW (1999) Three species of Microthyrium from Nolina. Mycotaxon 70:7–16
Ramaley AW (2005) The connection of Dothidotthia aspera (Botryosphaeriaceae) to a hyphomycetous anamorphic fungus, Thyrostroma negundinis. Mycotaxon 94:127–132
Ramaley AW, Barr ME (1995) New dictyosporous species from leaves of Agavaceae. Mycotaxon 54:75–90
Rannala B, Yang Z (1996) Probability distribution of molecular evolutionary trees: a new method of phylogenetic inference. J Mol Evol 43:304–311
Ranghoo VM, Hyde KD (2000) Ascominuta lignicola, a new loculoascomycete from submerged wood in Hong Kong. Mycoscience 42:1–5
Read SJ, Moss ST, Jones EBG (1997) Ultrastructure of asci, ascospores and appendages of Massarina ramunculicola (Loculoascomycetes, Ascomycota). Bot Mar 40:465–471
Reddy PV, Patel R, White JF Jr (1998) Phylogenetic and developmental evidence supporting reclassification of cruciferous pathogens Phoma lingam and Phoma wasabiae in Plenodomus. Can J Bot 76:1916–1922
Reed M (1902) Two new ascomycetous fungi parasitic on marine algae. Univ Calif Publ Bot 1:141–164
Rehm H (1896) Ascomyceten: hysteriaceen und discomyceten. In: Rabenhorst’s L (ed) Kryptogamen–Flora von Deutschland, Oesterreich und der Schweiz, 2nd edn. Eduard Kummer, Leipzig, pp 1–56
Rehm H (1900) Beiträge zur Pilzflora von Südamerika VIII. Discomycetes (Nachtrag). IX. Hypocreaceae. X. Dothideaceae. Hedwigia 39:209–234
Reid J, Pirozynski KA (1966) Studies on the Patellariaceae. I. Eutrblidiella Sabina (De Not.) Hӧhn. Can J Bot 44:655–662
Reid J, Pirozynski KA (1966) Notes on some interesting North American Fungi. Can J Bot 44:649–652
Renobales G, Aguirre B (1990) The nomenclature and systematic position of the genus Encephalographa. Syst Ascomycetum 8:87–92
Reynolds DR (1971) The sooty mold ascomycetes genus Limacinula. Mycologia 63:1173–1209
Reynolds DR (1982) Foliicolous ascomycetes: 4. The capnodiaceous genus Trichomerium Spegazzini emend. Mycotaxon 14:189–220
Reynolds DR (1986) Folliicolous ascomycetes 7. Phylogenetic Systematics of the Capnodiaceae. Mycotaxon 27:377–403
Reynolds DR, Gilbert GS (2005) Epifoliar fungi from Queensland, Australia. Aust Syst Bot 18:265–289
Reynolds DR, Gilbert GS (2006) Epifoliar fungi from Panama. Cryptogam Mycol 27:249–270
Riddle LW (1917) Pyrenothrix nigra gen. et spec. nov. Bot Gaz 64:513–515
Riddle LW (1920) Observations on the genus Acrospermum. Mycologia 12:175–181
Riddle LW (1923) The lichens of the Isle of Pines. Mycologia 15:68–88
Ridley GS, Ramsfield TD (2006) Elsinoё takoropuku sp. nov. infects twigs of Pittosporum tenuifolium in New Zealand. Mycologia 97:1362–1364
Riedl H (1961) Die Arten der Gattung Mycoporellum Mull. Arg. sensu A. Zahlbruckner. Catal., nebst Bemerkungen zum System dothidealer Flechten. Sydowia 15:257–287
Rivas Plata E, Lumbsch HT, Lücking R (2012) A new classification for the lichen family Graphidaceae s.lat. (Ascomycota: Lecanoromycetes: Ostropales). Fungal Divers 52:107–121
Rodrigues KF, Samuels GJ (1994) Letendraeopsis palmarum, a new genus and species of Loculoascomycetes. Mycologia 86:254–258
Rogers DP (1953) Disposition of nomina generica conservanda for fungi. Taxon 2:29–32
Romero AI, Samuels GJ (1991) Studies on Xylophilous fungi from Argentina. VI. Ascomycotina on Eucalyptus viminalis (Myrtaceae). Sydowia 43:228–248
Rossman AY (1987) The Tubeufiaceae and similar Loculoascomycetes. Mycol Pap 157:1–71
Rossman AY, Mouchacca J, Samuels GJ (1994) Phillipsiella crescentiae comb. nov. and a redescription of P. atra, type of the genus Phillipsiella. Sydowia 46:66–74
Rossman AY, Samuels GJ, Rogerson CT, Lowen R (1999) Checklist of genera of Bionectriaceae, Hypocreaceae, Nectriaceae, with an account of excluded genera and species. Stud Mycol 42:1–215
Routien JB (1958) A new species of Teichosporella. Mycologia 50:117–120
Roux C (2009) Naetrocymbe saxicola, likeno kun Trentepohlia. Bull Soc Linnéenne Provence 60:127–142
Roux C, Triebel D (1994) Révision des espèces de Stigmidium et de Sphaerellothecium (champignons lichénicoles non lichénisés, Ascomycetes) correspondant à Pharcidia epicymatia sensu Keissler ou à Stigmidium schaereri auct. Bull Soc Linéenne de Provence 45:451–542
Ruibal C, Gueidan C, Selbmann L, Gorbushina AA, Crous PW, Groenewald JZ, Muggia L, Grube M, Isola D, Schoch CL, Staley JT, Lutzoni F, de Hoog GS (2009) Phylogeny of rock–inhabiting fungi related to Dothideomycetes. Stud Mycol 64:123–133
Ryan BD, Bungartz F, Hagedorn G, Rambold G (eds) (2005 onwards) LIAS glossary. A Wiki–based online dictionary for ascomycete terminology used by LIAS, the global information system for lichenized and non–lichenized ascomycetes. http://glossary.lias.net/
Saccardo PA (1875) Grevillea 4(29):21
Saccardo PA (1877) Fungi venetino vive criticive Mycologiae Venetae addendi. Michelia 1–72
Saccardo PA (1878) Fungi Veneti novi vel critici vel mycologiae Venetae addendi. Ser. IX. Michelia 1(4):407
Saccardo PA (1880) Fungi Gallici ser. II. Michelia 2:39–135
Saccardo PA (1882) Sylloge Fungorum 1, Padova, p 766
Saccardo PA (1883) Sylloge Fungorum. 2, Italy, Patavii, pp 1–815
Saccardo PA (1891) Sylloge Fungorum 9, Italy, Pavia, p 1141
Saccardo PA, Paoletti G (1888) Mycetes Malacenses. Funghi della penisola di Malacca raccolti nel 1885 dell’ Ab. Benedetto Scortechini 6:387–428
Saccardo PA, Saccardo D (1905) Supplementum universale. Pars VI. Hymenomycetae–Laboulbeniomycetae. Syll Fung 17:860
Saccardo PA, Sydow P (1899) Sylloge Fungorum 14(1):1–724
Saccardo PA, Sydow P (1902) Supplementum Universale, Pars V. Syll Fung 16:1–1291
Saccardo PA, Trotter A (1913) Supplementum Universale Pars IX. Sylloge Fungorum 22:1–1612
Saenz GS, Taylor JW (1999) Phylogenetic relationships of Meliola and Meliolina inferred from nuclear small subunit rRNA sequences. Mycol Res 103:1049–1056
Samson RA, Mouchacca J (1975) Two new soil–borne cleistothecial ascomycetes. Can J Bot 53:1634–1639
Samuels GJ, Romero AI (1991) Ascoporia (Fungi, Loculoascomycetes), a new genus from Para. Bol Museu Paraense Emilio Goeldi Ser Bot 7:263–268
Samuels GJ, Muller E (1979) Life history of Brazilian ascomycetes 6. Sydowia 31:180–193
Sanchez RM, Bianchinotti MV (2010) New records in the Tubeufiaceae from Andean Patagonian forests of Argentina. Mycotaxon 111:131–141
Sánchez RM, Miller AN, Bianchinotti MV (2012) A new species of Acanthostigma (Tubeufiaceae, Dothideomycetes) from the southern hemisphere. Mycologia 104:223–231
Sanderson NA, Coppins BJ (2009a) Mycoporum. In: Smith CW, Aptroot A, Coppins BJ, Fletcher A, Gilbert OL, James PW, Wolseley PA (eds) The lichens of Great Britain and Ireland. British Lichen Society, London, pp 620–622
Sanderson NA, Coppins BJ (2009b) Tomasellia. In: Smith CW, Aptroot A, Coppins BJ, Fletcher A, Gilbert OL, James PW, Wolseley PA (eds) The lichens of Great Britain and Ireland. British Lichen Society, London, pp 894–895
Sanderson NA, Hawksworth DL, Aptroot A (2009) Melaspilea Nyl. In: The lichens of Great Britain and Ireland. British Lichen Society pp 576–579
Sankaran KV, Sutton BC (1991) Compsosporiella deightonii gen. et sp. nov. (Coelomycetes) from Sierra Leone. Mycol Res 11:1289–1293
Santesson R (1952) Foliicolous lichens I. A revision of the taxonomy of the obligately foliicolous, lichenized fungi. Symbolae Botanicae Upsalienses 12:1–590
Sawada K (1959) Descriptive catalogue of Taiwan (Formosan) fungi. Part XI. Spec Publ Coll Agric National Taiwan Univ 8:1–268
Schatz S (1984) The life history, developmental morphology, and taxonomy of Lautitia danica gen. nov. comb. nov. Can J Bot 62:28–32
Scheinpflug H (1958) Untersuchungen über die Gattung Didymosphaeria Fuck. und einige verwandte Gattungen. Ber Schweizerischen Botanischen Ges 68:325–385
Scheuer C (1991) Massarina tetraploa sp. nov. the teleomorph of Tetraploa aristata. Mycol Res 95:126–128
Scheuer C, Nograsek A (1993) Trematosphaeria pachycarpa and Herbampulla crassirostris gen. et spec. nov. (Ascomycetes). Mycotaxon 47:415–424
Schilling F (1927) Entwicklungsgeschichtliche und systematische Untersuchungen epiphyller Flechten. Hedwigia 67:269–300
Schmitt I, Mueller G, Lumbsch HT (2005) Ascoma morphology is homoplaseous and phylogenetically misleading in some pyrenocarpous lichens. Mycologia 97:362–374
Schoch CL, Shoemaker RA, Seifert KA, Hambleton S, Spatafora JW, Crous PW (2006) A multigene phylogeny of the Dothideomycetes using four nuclear loci. Mycologia 98:1041–1052
Schoch CL, Crous PW, Groenewald JZ, Boehm EWA, Burgess TI, de Gruyter J, de Hoog GS, Dixon LJ, Grube M, Gueidan C, Harada Y, Hatakeyama S, Hirayama K, Hosoya T, Huhndorf SM, Hyde KD, Jones EBG, Kohlmeyer J, Kruys 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, Rivas Plata E, Robbertse B, Ruibal C, Sakayaroj J, Sano T, Selbmann L, Shearer CA, Shirouzu T, Slippers B, Suetrong S, Tanaka K, Volkmann-Kohlmeyer B, Wingfield MJ, Wood AR, Woudenberg JHC, Yonezawa H, Zhang Y, Spatafora JW (2009a) A class–wide phylogenetic assessment of Dothideomycetes. Stud Mycol 64:1–15
Schoch CL, Sung GH, López-Giráldez F, Townsend JP, Miadlikowska J, Hofstetter V, Robbertse B, Matheny PB, Kauff F, Wang Z, Gueidan C, Andrie RM, Trippe K, Ciufetti LM, Wynns A, Fraker E, Hodkinson BP, Bonito G, Groenewald JZ, Arzanlou M, de Hoog GS, Crous PW, Hewitt D, Pfister DH, Peterson K, Gryzenhout M, Wingfield MJ, Aptroot A, Suh SO, Blackwell M, Hillis DM, Griffith GW, Castlebury LA, Rossman AY, Lumbsch HT, Lücking R, Büdel B, Rauhut A, Diederich P, Ertz D, Geiser DM, Hosaka K, Inderbitzin P, Kohlmeyer J, Volkmann-Kohlmeyer B, Mostert L, O’Donnell K, Sipman H, Rogers JD, Shoemaker RA, Sugiyama J, Summerbell RC, Untereiner W, Johnston PR, Stenroos S, Zuccaro A, Dyer PS, Crittenden PD, Cole MS, Hansen K, Trappe JM, Yahr R, Lutzoni F, Spatafora JW, Schoch CL et al (2009b) The Ascomycota tree of life: a phylum–wide phylogeny clarifies the origin and evolution of fundamental reproductive and ecological traits. Syst Biol 58:224–239
Schubert K, Ritschel A, Braun U (2003) A monograph of Fusicladium s. lat. (hyphomycetes). Schlechtendalia 9:1–132
Seaver FJ, Chardón CE (1926) Botany of Porto Rico and the Virgin Islands. Mycology. Scientific Survey of Porto Rico and the Virgin Islands 1:40–41
Seifert K, Morgan-Jones G, Gams W, Kendrick B (2011) The genera of hyphomycetes. CBS–KNAW Fungal Biodiversity Centre, Utrecht
Selbmann L, de Hoog GS, Gerrits van den Ende AHG, Ruibal C, De Leo F, Zucconi L, Isola D, Ruisi S, Onofri S (2005) Drought meets acid: three new genera in a Dothidealean clade of extremotolerant fungi. Stud Mycol 61:1–20
Sérusiaux E, Aptroot A (1998) A further new species of Monoblastia (lichenized Ascomycetes: Monoblastiaceae) from Papua New Guinea. Nova Hedwigia 67:259–265
Sérusiaux E, Lücking R (2003) The lichen genus Caprettia Bat. & H. Maia (Monoblastiaceae). Bibl Lichenologica 86:161–176
Shearer CA (1993) A new species of Kirschsteiniothelia (Pleosporales) with an unusual fissitunicate ascus. Mycologia 85:963–969
Shearer CA, Crane JL (1980) Taxonomy of two cleistothecial ascomycetes with papilionaceous ascospores. Trans Br Mycol Soc 75:193–200
Shearer CA, Hyde KD (1997) Massarina ingoldiana, a new ascomycete from freshwater habitats. Mycologia 89:114–119
Shearer CA, Crane JL, Redy KRC (1990) Studies in Leptosphearia. Lectotypification of Sphaeria dolioum. Mycologia 82:496–500
Shearer CA, Raja HA, Miller AN, Nelson P, Tanaka K, Hirayama K, Marvanova L, Hyde KD, Zhang Y (2009) The molecular phylogeny of freshwater Dothideomycetes. Stud Mycol 64:145–153
Shenoy BD, Jeewon R, Wu WP, Bhat DJ, Hyde KD (2006) Ribosomal an dRPB2 DNA sequence analyses suggest that Sporidesmium and morphologicaly similar genera are polyphyletic. Mycol Res 110:916–928
Sherwood MA (1977) The ostropalean fungi. Mycotaxon 5:1–277
Sherwood MA (1979) Helochora, a new genus of Polystigmataceae. Mycologia 71:648–651
Sherwood-Pike M, Boise J (1986) Studies in lignicolous ascomycetes: Xylopezia and mycowinteria. Brittonia 38:35–44
Shoemaker RA (1963) Generic correlations and concepts: Griphosphaerioma and Labridella. Can J Bot 41:1419–1423
Shoemaker RA, Babcock CE (1989) Phaeosphaeria. Can J Bot 67:1500–1599
Shoemaker RA, Babcock CE (1992) Applanodictyosporous Pleosporales: Clathrospora, Comoclathris, Graphyllium, Macrospora, and Platysporoides. Can J Bot 70:1618
Shoemaker RA, Egger KN (1982) Piedraia hortae. Fungi Canadenses 211:1–2
Shoemaker RA, Holm L, Eriksson OE (2003) Proposal to conserve the name Dothidea with a conserved type (Fungi: Dothideomycetes). Taxon 52:623–625
Sierra DL (2006) Contribución al estudio de los Ascomicetes bitunicados de Botanica Barcinonensia 50:5–434
Sigler L, Lumley TC, Currah RS (2000) New species and records of saprophytic ascomycetes (Myxotrichaceae) from decaying logs in the boreal forest. Mycoscience 41:495–502
Silva-Hanlin DMW, Hanlin RT (1999) Small subunit ribosomal RNA gene phylogeny of several Loculoascomycetes and its taxonomic implications. Mycol Res 103:153–160
Simon UK, Groenewald JZ, Crous PW (2009) Cymadothea trifolii, an obligate biotrophic leaf parasite of Trifolium, belongs to Mycosphaerellaceae as shown by nuclear ribosomal DNA analyses. Persoonia 22:49–55
Sivanesan A (1977) The taxonomy and pathology of Venturia species. Lubrecht & Cramer Ltd, Vaduz, 138
Sivanesan A (1981) Balladynopsis, Balladynocallia and Alina. Mycol Pap 146:1–38
Sivanesan A (1984) The bitunicate ascomycetes and their anamorphs. J. Cramer, Vaduz, p 701
Sivanesan A (1996) Corynesporasca caryotae gen. et sp. nov. with a Corynespora anamorph, and the family Corynesporascaceae. Mycol Res 100:783–788
Sivanesan A, Hsieh WH (1989) Kentingia and Setocampanula, two new ascomycete genera. Mycol Res 93(1):83–90
Slippers B, Crous PW, Denman S, Coutinho TA, Wingfield BD, Wingfield MJ (2004) Combined multiple gene genealogies and phenotypic characters differentiate several species previously identified as Botryosphaeria dothidea. Mycologia 96:83–101
Smith CW, Aptroot A, Coppins BJ, Fletcher A, Gilbert OL, James PW, Wolseley PA (eds) (2009) The lichens of Great Britain and Ireland. The British Lichen Society, London, p 1046
Spatafora JW, Owensby CA, Douhan G, Boehm EWA, Schoch C (2011) Phylogenetic placement of Cenococcum in Gloniaceae (Dothideomycetes). Mycologia 104:758–765
Speer EO (1986) A propos de champignons du Brésil III. Mytilidion resinae sp. nov. (Hysteriales) et sa forme conidienne, Camaroglobulus resinae gen. et spec. nov. (Sphaeropsidales). Bull Trimest Soc Mycol Fr 102:97–100
Spegazzini C (1879) Nova addenda ad mycologiam venetam. Michelia 1:453–487
Spegazzini (1880) Pleomassaria. Anales de la Sociedad Científica Argentina. 9: (in tabula ad p 192)
Spegazzini C (1889a) Fungi Puiggariani. Pugillus 1. Bol Acad Nac Cienc Córdoba 11(4):381–622
Spegazzini C (1889b) Fungi nonnulli. Paraguariae Fuegiae–Rev Mycol Toulouse (Toulouse) 11(42):93–95
Spegazzini C (1909) Mycetes Argentinenses. Series IV. Anales del Museo Nacional de Historia Natural Buenos Aires 19:257–458
Spooner BM, Kirk PM (1990) Observations on some genera of Trichothyriaceae. Mycol Res 94:223–230
Stamatakis A (2006) RAxML-VI-HPC: Maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models. Bioinformatics 22:2688–2690
Stamatakis A, Hoover P, Rougemont J (2008) A rapid bootstrap algorithm for the RAxML Web Servers. Syst Biol 57:758–771
Starbäck K (1899) The Myriangiales Bihang till Kongliga Svenska Vetenskaps Academien Handlingar 25:3–37
Stenroos S, Laukka T, Huhtinen S, Döbbeler P, Myllys L, Syrjänen K, Hyvönen J (2010) Multiple origins of symbioses between ascomycetes and bryophytes suggested by a five–gene phylogeny. Cladistics 26:281–300
Stevens FL (1917) Porto Rican fungi, old and new. Trans Illinois State Acad Sci 10:162–218
Stevens FL (1925) Hawaiian fungi. Bull Bernice P Bishop Museum Honolulu 19:1–189
Stizenberger E (1862) Beitrag zur Flechtensystematik. Ber über die Thätigkeit Sankt Gallischen Natuwiss Ges 124–182
Stone RE (1912) The life history of Ascochyta on some leguminous plants. Ann Mycol 10:564–592
Su D, Ru-jun Z, Xue-rui Y, Shu-yi Y, Jun-Fan F (2012) Infection and establishment of Ascochyta anemones in leaves of windflower. Afr J Microbiol Res 6:4983–4988
Suetrong S, Jones EBG (2006) Marine discomycetes: a review. Indian J Mar Sci 35:291–296
Suetrong S, Schoch CL, Spatafora JW, Kohlmeyer J, Volkmann-Kohlmeyer B, Sakayaroj J, Phongpaicht S, Tanaka K, Hairayama K, Jones EBG (2009) Molecular systematics of the marine Dothideomycetes. Stud Mycol 64:155–173
Suetrong S, Sakayaroj J, Phongpaichit S, Jones EBG (2010) Morphological and molecular characteristics of a poorly known marine ascomcycete, Manglicola guatamalensis (Jahnulales: Pezizomycotina; Dothideomycetes, Incertae sedis): new lineage of marine ascomycetes. Mycologia 102:83–92
Suetrong S, Boonyue N, Pang KL, Ueapattanakit J, Klaysuban A, Sri-Inddrasutdhi V, Sivichai S, Jones EBG (2011a) A taxonomic revision and phylogenetic reconstruction of the Jahnulales (Dothideomycetes), and the new family Manglicolaceae. Fungal Divers 51:163–188
Suetrong S, Hyde KD, Ahang Y, Bahkali AB, Jones EBG (2011b) Trematosphaeriaceae fam. nov. (Dothideomycetes, Ascomycota). Cryptogam Mycol 32:343–358
Suh SO, Blackwell M (1999) Molecular phylogeny of the cleistothecial fungi placed in Cephalothecaceae and Pseudeurotiaceae. Mycologia 91:836–845
Sutton BC (1970) Glyphium leptothecium (Earle) comb. nov. G. schizosporum (Maire) Zogg, and their imperfect states. Trans Br Mycol Soc 54:255–264
Sutton BC (1980) The Coelomycetes. Fungi Imperfecti with Pycnidia, Acervuli and Stromata. Commonwealth Mycological Institute pp 1–696
Sutton BC, Alcorn JL (1983) Sarcinulella banksiae gen. et sp. nov. a coelomycete with a unique method of conidial dispersal. Mycotaxon 16:557–564
Sutton BC, Pollok FG (1973) Gleosporium cercocarpi and Sphaceloma cercocarpi. Mycologia 65:1125–1134
Swart HJ (1971) Australian leaf–inhabiting fungi I. Two species of Vizella. Trans Br Mycol Soc 57:455
Swart HJ (1987) Australian leaf–inhabiting fungi. XXV. Dothidellainaequalis and Montagnellaeucalypti. Trans Br Mycol Soc 89:483
Swart L, Crous PW, Kang JC, Mchau GRA, Pascoe I, Palm ME (2001) Differentiation of species of Elsinoё associated with scab disease of Proteaceae based on morphology, symptomatology, and ITS sequence phylogeny. Mycologia 93:366–379
Sweetwood G, Lücking R, Nelsen MP, Aptroot A (2012) Ascospore ontogeny and discharge in megalosporous Trypetheliaceae and Graphidaceae (Ascomycota: Dothideomycetes and Lecanoromycetes) suggest phylogenetic relationships and ecological constraints. Lichenologist 44:277–296
Swinscow TDV (1965) Pyrenocarpous lichens: 9. Notes on various species. Lichenologist 3:72–83
Swinscow TDV (1970) Pyrenocarpous lichens: 14. Arthopyrenia Massal. sect. Acrocordia (Massal.) Müll. Arg. in the British Isles. Lichenologist 4:218–233
Swofford DL (2002) PAUP: phylogenetic analysis using parsimony, version 4.0 b10. Sinauer Associates, Sunderland
Sydow H (1925) Fungi in itinere costaricensi collecti. Pars prima. Ann Mycol 23:308–429
Sydow H (1953) Fungi venezuelani–Additamentum. Ann Mycol 33:85–100
Sydow H, Sydow P (1912) Beschreibungen neuer südafrikanischer. Ann Mycol 10:33–45
Sydow H, Sydow P (1916) Weitere Diagnosen neuer philippinischer Pilze. Ann Mycol 14:353–375
Takashi Y, Sano A, Yarita K, Suh MK, Nishimura K, Udagawa S (2006) A new species of Cephalotheca isolated from a Korean patient. Mycotaxon 96:309–322
Tam WY, Pang KL, Jones EBG (2003) Ordinal placement of selected marine Dothideomycetes inferred from SSU ribosomal DNA sequence analysis. Bot Mar 4:487–494
Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28(10):2731–2739
Tanaka K, Harada Y (2003a) Pleosporales in Japan (1): the genus Lophiostoma. Mycoscience 44:85–96
Tanaka K, Harada Y (2003b) Pleosporales in Japan (2): Lophiotrema. Mycoscience 44:115–121
Tanaka K, Harada Y (2003c) Pleosporales in Japan (3). The genus Massarina. Mycoscience 44:173–185
Tanaka K, Harada Y (2005) Bambusicolous fungi in Japan (6): Katumotoa, a new genus of phaeosphaeriaceous ascomycetes. Mycoscience 46:313–318
Tanaka K, Hosoya T (2008) Lophiostomasagittiforme sp. nov., a new ascomycete (Pleosporales, Dothideomycetes) from Island Yakushima in Japan. Sydowia 60:131–145
Tanaka K, Ooki Y, Hatakeyama S, Harada Y, Barr ME (2005) Pleosporales in Japan (5): Pleomassaria, Asteromassaria, and Splanchnonema. Mycoscience 46:248–260
Tanaka K, Hirayama K, Yonezawa H, Hatakeyama S, Harada Y, Sano T, Shirouzu T, Hosoya T (2009) Molecular taxonomy of bambusicolous fungi: Tetraplosphaeriaceae, a new pleosporalean family with Tetraploa–like anamorphs. Stud Mycol 64:175–209
Tanaka K, Mel’nik VA, Kamiyama M, Hirayama K, Shirouzu T (2010) Molecular phylogeny of two coelomycetous fungal genera with stellate conidia, Prosthemium and Asterosporium, on Fagales trees. Botany 88:1057–1071
Taylor JE, Groenewald JZ, Crous PW (2003) A phylogenetic analysis of Mycosphaerellaceae leaf spot pathogens of Proteaceae. Mycol Res 107(6):653–658
Tehler A (1990) A new approach to the phylogeny of Euascomycetes with a cladistic outline of Arthoniales focussing on Roccellaceae. Can J Bot 68(11):2458–2492
Tehler A (1995) Morphological data, molecular data, and total evidence in phylogenetic analysis. Can J Bot 73(suppl 1):S667–S676
Tendulkar JS (1971) Mode of sexual reproduction and early development in Parodiella paraguyensis Speg. Nova Hedwigia 21:269–277
Teng SC (1933) Notes on Hysteriales from China. Sinensia 4:129–144
Teodoro MG, Ferreira MA, Guimarães LMS, Mafia RG, Groenewald JZ, Crous PW, Alfenas AC (2012) Mycosphaerella and Teratosphaeria species associated with leaf diseases on Eucalyptus globulus in southern Brazil. Phytopathol Mediterr 51:355–364
Theissen F (1914a) Annotacöes á mycoflora Brasileira. Broteria 12:13–31
Theissen F (1914b) Die Trichothyriaceen. Beihefte Botanischen Zentralbl 32(Abt. II):1–16
Theissen F (1916) Mykologische Abhandlungen. Verh K-Kg Zool-Botanischen Ges Wien 66:296–400
Theissen F, Sydow H (1915) Die Dothideales. Kritisch-systematische riginaluntersuchungen. Ann Mycol 13:147–746
Theissen F, Sydow H (1917) Synoptische Tafeln. Ann Mycol 15:389–491
Theissen F, Sydow H (1918) Vorentwurfe zu den Pseudosphaeriales. Ann Mycol 16:1–34
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG (1997) The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic acids research 25(24):4876
Tilak ST (1963) Ascomycetes on Celastrus paniculata Willd. Mycopatholgia 21:60–63
Timmer LW, Priest M, Broadbent P, Tan MK (1996) Morphological and pathological characterization of species of Elsinoё causing scab diseases of Citrus. Phytopathology 86:1032–1038
Tode HJ (1784) Beschreibung des Venusschwammes (Hysterium). Schriften Berl Ges Naturforschender Freunde 5:53–55
Tode HJ (1790) Fungi Mecklenburgenses Selecti. Fasc. 1. Nova Fungorum Genera Complectens. i-viii, 1–50, plates 1–7
Tomaselli R, Ciferri R (1952) Scissioni di generi di licheni sulla base delle caratteristiche del fungo. Arch Bot Ital 28:1–15
Toro RA (1926) Mixomicetos de Santo Domingo coleccionados por F. D. Kern y R. A. Toro Estacion Agronomica de Haina, Serie B, Botanica 6. pp 7
Toro RA (1952) A study of the tropical American black–mildews. J Agric Univ P R 36:24–87
Toxopeus J, Kozera CJ, O’Leary SJB, Garbary DJ (2011) A reclassification of Mycophycias ascophylli (Ascomycota) based on nuclear large ribosomal subunit DNA sequences. Bot Mar 54:325–334
Tretiach M, Modenesi P (1999) Critical notes on the lichen genus Encephalographa A. Massal. (Hysteriaceae). Nova Hedwigia 68:527–544
Triebel D (1989) Lecideicole Ascomyceten. Eine Revision der obligat lichenicolen Ascomyceten auf lecideoiden Flechten. Bibliotheca Lichenologica, No. 35. J. Cramer, Berlin–Stuttgart p 278
Tsui CKM, Berbee ML (2006) Phylogenetic relationships and convergence of helicosporous fungi inferred from ribosomal DNA sequences. Mol Phyl Evol 39:587–597
Tsui CKM, Sivichai S, Berbee ML (2006) Molecular systematics of Helicoma, Helicomyces and Helicosporium and their teleomorphs inferred from rDNA sequences. Mycologia 98:94–104
Tsui CKM, Sivichai S, Rossman AY, Berbee ML (2007) Tubeufia asiana, the teleomorph of Aquaphila albicans in the Tubeufiaceae, Pleosporales, based on cultural and molecular data. Mycologia 99:884–894
Tsuneda A, Hambleton S, Currah RS (2004) Morphology and phylogenetic placement of Endoconidioma, a new endoconidial genus from trembling aspen. Mycologia 96:1128–1135
Tsuneda A, Davey ML, Tsuneda I, Currah RS (2010) Two new dothideomycetous endoconidial genera from declining larch. Botany 88:471–487
Tucker SC, Harris RC (1980) New or noteworthy pyrenocarpous lichens from Louisiana and Florida. Bryologist 83:1–20
Tulasne LR, Tulasne C (1863) Selecta Fungorum Carpologia, vol. 2, 319 pages, 34 Pl. Paris
Tulasne LR, Tulasne C (1931) Selecta Fungorum Carpologia of the brothers L. R. and C. Tulasne. Translated into English by W. B. Grove. In: Reginald Buller AH, Shear CL (eds) Volume two [1863]: Xylariei. Valsei. Sphaeriei. With thirty four copper plates. Oxford
Ullasa BA (1969) Ascospore germination in Parodiella. Trans Br Mycol Soc 53:319–321
Vainio E (1921) Lichenes ab A. Yasuda in Japonia collecti. Continuatio I. Bot Mag (Tokyo) 25:45–79
van der Aa HA, Noordeloos ME, DE Gruyter J (1990) Species concepts in some larger genera of the coelomycetes. Stud Mycol 32:3–19
van der Linde EJ (1992) Notes on the South African Hysteriaceae (Ascomyctes: Mycotina). S Afr J Bot 58:491–499
van Geel B, Buurman J, Brinkkemper O, Schelvis J, Aptroot A, van Reenen G, Hakbijl T (2003) Environmental reconstruction of a Roman Period settlement site in Uitgeest (The Netherlands), with special reference to coprophilous fungi. J Archaeol Sci 30:873–883
van Niekerk JM, Crous PW, Groenewald JZ, Fourie PH, Halleen F (2004) DNA phylogeny, morphology and pathogenicity of Botryosphaeria species on grapevines. Mycologia 96:781–798
van Ryckegem G, Aptroot A (2001) A new Massarina and a new Wettsteinina (Ascomycota) from freshwater and tidal reeds. Nova Hedwigia 73:161–166
van Warmelo KT (1966) The identity of a pea blight fungus in South Africa. Bothalia 9:183–194
van Wyk PS, Marasas WFO, Hattingh MJ (1976) Morphology and taxonomy of Vizella interrupta (Ascomycetes: Vizellaceae). Trans Br Mycol Soc 66:489–494
Vasilyeva LN (2000) Hysteriaceous fungi in the Russian Far East III. Glonium and Actidiographium. Mikol Fitopatol 34:3–5
Vasilyeva LN (2001) Hysteriaceous fungi in the Russian Far East IV. Glyphium, Lophium and Mytilinidion. Mikol Fitopatol 35:15–18
Verkley GJM, Priest MJ (2000) Septoria and similar coelomycetous anamorphs of Mycosphaerella. Stud Mycol 45:123–128
Verkley GJM, Starink-Willemse M, Van Iperen A, Abeln ECA (2004) Phylogenetic analyses of Septoria species based on the ITS and LSU–D2 regions of nuclear ribosomal DNA. Mycologia 96:558–571
Verkley GJM, Quaedvlieg W, Shin H-D, Crous PW (2013) A new approach to species delimitation in Septoria. Stud Mycol 75:213–305
Vézda A (1975) Foliikole Flechten aus Tanzania (Ost–Afrika). Folia Geobotanica Phytotaxonomica 10:383–432
Vézda A (1984) Foliikole Flechten der Insel Kuba. Springer 19(2):177–210
Vézda A (2004) Neue foliicole Flechten III. Acta Musei Richnoviensis. Sect Natur 11:57–72
Vidal P, Vinuesa MA, Sánchez-Puelles JM, Guarro J (2000) Phylogeny of the anamorphic genus Chrysosporium and related taxabased on rDNA internal transcribed spacer sequences. Rev Iberoam Micol 17:22–29
Viegas AP (1943) Piedraia Hortai (Brumpt) Fonseca & Area Leao. Bragantia 3:37–40
Voglmayr H, Jaklitsch WM (2011) Molecular data reveal high host specificity in the phylogenetically isolated genus Massaria (Ascomycota, Massariaceae). Fungal Divers 46:133–170
Von Arx JA (1952) Studies on Venturia and related genera. Tijdschr Plantenziekten 58:260–266
von Arx JA (1963) Die Gattungen der Myriangiales. Persoonia 2(4):421–475
von Arx JA (1971) Testudinaceae, a new family of Ascomycetes. Persoonia 6:365–369
von Arx JA, Müller E (1954) Die Gattungen der amerosporen Pyrenomyceten. Beitr Kryptogamenflora Schweiz 11:1–434
von Arx JA, Müller E (1975) A re-evaluation of the bitunicate Ascomycetes with keys to families and genera. Stud Mycol 9:1–159
von Arx JA, van der Aa HA (1983) Notes on Curreya (Ascomycetes, Dothideales). Sydowia 36:1–5
Von Höhnel F (1905) Mycologische Fragmente. LXXVII-XCVII. Ann Mycol 3:323–339
von Höhnel FXR (1909a) Fragmente zur Mykologie: VII. Mitteilung (Nr. 289 bis 353). Sber Akad Wiss Wien Math–Naturw K l(118):847–848
von Höhnel FXR (1909b) Fragmente zur Mykologie VIII. Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in Wien Mathematische–Naturwissenschaftliche Klasse, Abt 1(118):1157–1246
von Höhnel FXR (1909c) Fragmente zur Mykologie: VI. Mitteilung (Nr. 182 bis 288). Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in Wien Mathematische–Naturwissenschaftliche Klasse, Abt I. 118:275–452
von Höhnel FXR (1910a) Fragmente zur Mykologie: X. Mitteilung (Nr. 468 bis 526). Sitzungsberichte der Kaiserlichen Akademie der Wissenschaften Math.–naturw. Klasse Abt. I, 119:393–473
von Höhnel F (1910b) Fragmente zur Mykologie: X. Mitteilung (Nr. 468 bis 526). Sber Akad Wiss Wien Math Naturw Kl 119:393–473
von Höhnel FXR (1911) Fragmente zur Mykologie (XIII. Mitteilung, Nr. 642 bis 718). Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in Wien Mathematische–Naturwissenschaftliche Klasse. I. 120:379–384
von Höhnel FXR (1917) System der Phacidiales v. H. Sonderabdruck. Ber Dtsch Bot Ges 25:416–422
von Höhnel FXR (1918a) Mycologische Fragmente, 272. Über die Hysteriaceen. Ann Mycol 16:145–154
von Höhnel FXR (1918b) Fragmente zur Mykologie. Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in WienMathematische–Naturwissenschaftliche Klasse, Abt. 1(127):329–393
von Höhnel FXR (1919) Fragmente zur Mykologie. XXII Mitteilungen, nr. 1092 bis 1153. Sitzungsberichten der Kaiserliche Akademie der Wissenschaften in Wien Mathematische–Naturwissenschaftliche Klasse, Abt 1(128):549–634
von Höhnel FXR (1928) In Saccardo, Leptopeltineae v. H Syll fung (Abellini) 24(2):1255
von Keissler K (1934) Moriolaceae, Epigloeaceae. In: Rabenhorst GL, Kryptogamen–Flora von Deutschland, Österreich und der Schweiz. 2nd IX, Die Flechten, Abt. 1 (2). Borntraeger\Leipzig, pp 1–43
von Thümen F (1877) Symbolaead floram mycologicam austriacam. Österr Bot Z 27:270–272
Wakefield EM (1940) Nomina generica conservanda. Contributions from the Nomenclature Committee of the British Mycological Society. III. Trans Br Mycol Soc 24:282–293
Wang HK, Aptroot A, Crous PW, Hyde KD, Jeewon R (2007) The polyphyletic nature of Pleosporales: an example from Massariosphaeria based on rDNA and RBP2 gene phylogenies. Mycol Res 111:1268–1276
Watson W (1929) The classification of lichens. New Phytol 28:85–115
Webster J (1956) Conidia of Acrospermum compressum and A. graminum. Trans Br Mycol Soc 39(3):361–366
Webster J (1992) Anamorph–teleomorph relationships. In: Bärlocher F (ed) The ecology of aquatic hyphomycetes. Springer–Verlag 99–117
Wehmeyer LE (1941) A revision of Melanconis, Pseudovalsa, Prosthecium, and Titania. University of. Mich Stud: Sci Ser 14:1–161
Wehmeyer LE (1948) The developmental pattern within the genus Pleospora Rab. Mycologia 40:269–294
Wehmeyer LE (1957) The genus Montagnula Berl. Sydowia 1:257–263
Wehmeyer LE (1961) A world monograph of the genus Pleospora and its segregates. University of Michigan, Ann Arbor, p 451
Wehmeyer LE (1975) The pyrenomycetous fungi. Mycologia Memoir No. 6. The New York Botanical Garden. J. Cramer Publishing, Germany
Welch DS (1926) A monographic study of genus Cucurbitaria in North America. Mycologia 1851–86
Wiens JJ (2006) Missing data and the design of phylogenetic analyses. J Biomed Inform 39:34–42
Wijayawardene DNN, McKenzie EHC, Hyde KD (2012) Towards incorporating anamorphic fungi in a natural classification checklist and notes for 2011. Mycosphere 3:157–228
Wijayawardene DNN, Song Y, Bhat DJ, McKenzie EHC, Chukeatirote E, Wang Y, Hyde KD (2013) Wojnowicia viburni sp. nov. from China and its phylogenetic placement. Sydowia 65(1):113–128
Wikee S, Udayanga D, Crous PW, Chukeatirote E, McKenzie EHC, Bahkali AH, Dai DQ, Hyde KD (2011) Phyllosticta an over–view of current status of species recognition. Fungal Divers 51:43–61
Wikee S, Lombard L, Nakashima C, Motohashi K, Chukeatirote E, Cheewangkoon R, McKenzie EHC, Hyde KD, Crous PW (2013) A phylogenetic re-evaluation of Phyllosticta (Botryosphaeriales). Studies in Mycology 76:1–29
Willoughby LG, Archer JF (1973) The fungal spora of a freshwater stream and its colonization pattern on wood. Freshw Biol 3:219–239
Wingfield MJ, de Beer ZW, Slippers B, Wingfield BD, Groenewald JZ et al (2012) One fungus one name promotes progressive plant pathology. Mol Plant Pathol 13:604–613
Winka K, Eriksson OE, Bäng A (1998) Molecular evidence for recognizing the Chaetothyriales. Mycologia 90:822–830
Winter G (1885) Pilze–Ascomyceten. In: GL Rabenhorst’s Kryptogamen–Flora von Deutschland, Oesterreich und der Schweiz. 1:65–528
Winter G (1887) Ascomyceten. Rab Krypt Flora 1(2):1–928
Wolf FA, Wolf FT (1947). The Fungi 1: 438 pp., 153 figs. USA, New York; UK, London; Wiley, Chapman & Hall
Wong MH, Crous PW, Henderson J, Groenewald JZ, Drenth A (2012) Phyllosticta species associated with freckle disease of banana. Fungal Divers 56:173–187
Woronichin NN (1915) Les fumagines de Sotschi. Bull Appl Bot 8:769–807
Woronichin NN (1925) Über die Capnodiales. Ann Mycol 23:174–178
Woronichin NN (1926) Zur Kenntnis der Morphologie und Systematik der Russtaupilze Transkaukasiens. Ann Mycol 24:231–264
Woudenberg JHC, Groenewald JZ, Binder M, Crous PW (2013) Alternaria redefined. Stud Mycol 75:171–212
Wu HX, Jaklitsch WM, Voglmayr H, Hyde KD (2011a) Epitypification, morphology and phylogeny of Tothi fuscella. Mycotaxon 118:203–211
Wu HX, Schoch CL, Boonmee S, Bahkali AH, Chomnunti P, Hyde KD (2011b) A reappraisal of Microthyriaceae. Fungal Divers 51(1):189–248
Wulandari NF, To-anun C, Hyde KD, Duong LM, de Gruyter J et al (2009) Phyllosticta citriasiana sp. nov. the cause of Citrus tan spot of Citrus maxima in Asia. Fungal Divers 34:23–39
Yao YJ, Spooner BM (1999) Roesleriaceae, a new family of Ascomycota, and a new species of Roeslerina. Kew Bull 54:683–693
Yarwood CE (1973) Pyrenomycetes: Erysiphales. In: Ainsworth GC, Sparrow FK, Sussman A (eds) The fungi, vol. IVA. Academic, New York, pp 71–86
Yeshitela K, Fischer E, Killmann D, Sérusiaux E (2009) Aspidothelium hirsutum (Thelenellaceae) and Caprettia goderei (Monoblastiaceae), two new species of foliicolous lichens from Ethiopia and Kenya. Bryologist 112:850–855
Zahlbruckner A (1898) Beiträge zur Flechtenflora Niederösterreichs V. Verhandlungen der Kaiserlich-Königlichen Zoologisch-Botanischen Gesellschaft in Wien 48:349–370
Zahlbruckner A (1903) Lichenes, Spezieller Teil. In: Engler A, Prantl K (eds) Die Naturlichen Pflanzenfamilien, Abt. 1, t. 1. Engelmann, Leipzig. 49–249
Zahlbruckner A (1907) Mastodiaceae. In: Engler HGA, PrantlK AE (eds) Die natürlichen Pflanzenfamilien nebst ihren Gattungen und wichtigeren Arten insbesondere den Nutzpflanzen, unter Mitwirkung zahlreicher hervorragender Fachgelehrten I. Abteilung 1:240. Leipzig, Germany
Zahlbruckner A (1926) Catalogus Lichenum Universalis. Borntraeger, Leipzig
Zahlbruckner A (1935) Florida–Flechten, gesammelt von S. Rapp. Ann Mycol 33:33–45
Zalasky H (1968) Rhytidiella moriformis n. gen., n. sp. causing rough–bark of Populus balsamifera. Can J Bot 46:1383–1387
Zenker JK (1827) Lichenes. In: Goebel F, Kunze G (eds) Pharmazeutische Waarenkunde 1:109–199. Eisenach
Zhang M, Koko TW, Hyde KD (2011a) Towards a monograph of Dothideomycetes: Studies on Diademaceae. Cryptogam Mycol 32:115–126
Zhang Y, Hyde KD (2009) Transfer of Pseudoparodia pseudopeziza to Patellariaceae (Patellariales). Nova Hedwigia 88:211–215
Zhang Y, Fournier J, Pointing SB, Hyde KD (2008a) Are Melanomma pulvis–pyrius and Trematosphaeria pertusa congeneric? Fungal Divers 33:47–60
Zhang Y, Jeewon R, Fournier J, Hyde KD (2008b) Multi–gene phylogeny and morphotaxonomy of Amniculicola lignicola: a novel freshwater fungus from France and its relationships to the Pleosporales. Mycol Res 112:1186–1194
Zhang Y, Fournier J, Crous PW, Pointing SB, Hyde KD (2009a) Phylogenetic and morphological assessment of two new species of Amniculicola and their allies (Pleosporales). Persoonia 23:48–54
Zhang Y, Schoch CL, Fournier J, Crous PW, de Gruyter J, Woudenberg JHC, Hirayama K, Tanaka K, Pointing SB, Spatafora JW, Hyde KD (2009b) Multi–locus phylogeny of Pleosporales: a taxonomic, ecological and evolutionary re–evaluation. Stud Mycol 64:85–102
Zhang Y, Wang HK, Fournier J, Crous PW, Jeewon R, Pointing SB, Hyde KD (2009c) Towards a phylogenetic clarification of Lophiostoma, Massarina and morphologically similar genera in the Pleosporales. Fungal Divers 38:225–251
Zhang Y, Crous PW, Schoch CL, Bahkali AH, Guo LD, Hyde KD (2011b) A molecular, morphological and ecological re-appraisal of Venturiales-a new order of Dothideomycetes. Fungal Divers 51:249–277
Zhang Y, Crous PW, Schoch CL, Hyde KD (2012a) Pleosporales. Fungal Divers 53:1–221
Zhang Y, Fournier J, Phookamsak R, Bakhali AH, Hyde KD (2012b) Halotthiaceae fam. nov. (Ploepsorales) accommodates the new genus Phaeoseptum and several other aquatic genera. Mycologia 40:107–110
Zhang Y, Fournier J, Phookamsak R, Bahkali Ali H, Hyde KD (2013) Halotthiaceae fam. nov. (Pleosporales) accommodates the new genus Phaeoseptum and several other aquatic genera. Mycologia 105:603–609
Zhaxybayeva O, Gogarten JP (2002) Bootstrap, Bayesian probability and maximum likelihood mapping: exploring new tools for comparative genome analyses. BMC Genomics 3(1):4
Zhuang WY, Liu CY (2012) What an rRNA secondary structure tells about phylogeny of fungi in Ascomycota with emphasis on evolution of major types of ascus. PLoS One 7:e47546
Zogg H (1962) Die Hysteriaceae s. str. und Lophiaceae, unter besonderer Berücksichtigung der mitteleuropäischen Formen. Beitr Kryptogamenflora Schweiz Band 11:1–190
Zukal H (1890) Epigloea bactrospora. Eine neue Gallertflechte mit chlorophyllhältigen
Acknowledgments
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, PREM, S, TRTC, UBC, UC, UCR, UPS, URM, URM and W are especially thanked for sending and loaning herbarium specimens and for being very helpful when it came to locating specimens. Without their help this work would not have been possible. The abbreviations of herbarium are those listed in Index Herbariorum (2013). We also thank Siriporn Luesuwan for arranging the loan of specimens from various herbaria.
A. Ariyawansa and J.C Kang are grateful to the International collaboration plan of Science and Technology at Guizhou Province (contract No. [2012] 7006) and the construction of innovation talent team of Science and Technology at Guizhou Province (contract No. [2012]4007), China. D.J. Bhat is thankful to MFU for a Visiting Professorship during the tenure of which this paper was finalized. D.L.Hawksworth contributed to this work while in receipt of support from the Spanish Ministerio de Ciencia e Innovación (CGL2011-25003). Haixia Wu would like to thank the Grant for Essential Scientific Research of National Non–profit Institute to funds for research (No. CAFYBB2007002) and thanks Xiaoming Chen, Ying Feng and Chen Hang (The Research Institute of Resource Insects, Chinese Academy of Forestry, China) for their valuable help. Jian-Kui Liu would like to thank Manfred Binder for providing valuable suggestions and kind assistance on phylogenetic analysis. We would like to thank MFU grant No. 56101020032 for funding to study taxonomy and phylogeny of selected families of Dothideomycetes. Jiye Yan and Xinghong Li would like to thank CARS-30 for funds. K. Tanaka would like to thank the Japan Society for the Promotion of Science (JSPS, 25440199) for financial support. K.L. Pang would like to thank National Science Council of Taiwan for financial support (NSC101–2621–B–019–001–MY3). L. Muggia is grateful to the Austrian Science Foundation for financial support (FWF, P24114-B16 and Herta-Firnberg Project T481-B20). M. Doilom would like to thank the Thailand Research Fund through the Royal Golden Jubilee (RGJ) Ph.D. Program grant No. Ph.D./0072/2553 in 4.S.M.F./53/A.2. MP Nelsen and R Lücking are grateful to the NSF (DEB 0715660 “Neotropical Epiphytic Microlichens - An Innovative Inventory of a Highly Diverse yet Little Known Group of Symbiotic Organisms”; DEB 0717476 “Systematics of Dothideomycetes”); MP Nelsen also acknowledges a Brown Family Fellowship through the Field Museum, a William Harper Rainey Fellowship through the University of Chicago, and support through the Committee on Evolutionary Biology at the University of Chicago. R. Phookamsak would like to thank the Royal Golden Jubilee Ph. D. Program (PHD/0090/2551) under the Thailand Research Fund for scholarship support. S. A. Alias would like to thank Program Rakan University Malaya (PRPUM) - Phylogeny, Taxonomy, Relationships and Biotechnological Potential of Sooty Moulds. S. Boonmee also thanks Amy Y. Rossman and the U.S. Department of Agriculture Agricultural Research Service, Systematic Mycology and Microbiology Lab (SMML), USA for laboratory, funding support and advice on her work. S. Boonmee and P. Chomnunti would like to thank TRF/BIOTEC program Biodiversity Research and Training Grant BRT R_251181, BRT R_253012 and the Mushroom Research Foundation, Chiang Rai Province for funding support. S. Wikee would like to thank the Thailand Research Fund through the Royal Golden Jubilee Ph.D. Program agreement No PhD/0198/2552. S. Wikee and JK Liu would like to thank The National Research Council of Thailand (NRCT) for the award of grant No 55201020002 to study the genus Phyllosticta in Thailand. S. Suetrong acknowledges the financial support by TRF/BIOTEC program Biodiversity Research and Training Grant BRT R_351004 and BRT R_325015 to study marine fungi of Thailand. Suetrong also thanks Morakot Tanticharoen, Kanyawim Kirtikara and Lily Eurwilaichitr, BIOTEC, Bangkok for their continued interest and support. Supalak Yacharoen, J. Monkai and K.D. Hyde would like to thank the Thailand Research Fund (BRG5280002) for financial support. Gareth Jones is supported by the Distinguished Scientist Fellowship Program (DSFP), King Saud University, Saudi Arabia. Y. Wang would like to thank The International Scientific Cooperated Project of Guizhou Province (No [2013]7004). Yongxiang Liu would like to thank the Guizhou Research Fund (QKHZYZ[2010]5031 and QNKYYZX[2012]010) for financial support. Harrie Sipman is thanked for comments on part of the manuscript.
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Hyde, K.D., Jones, E.B.G., Liu, JK. et al. Families of Dothideomycetes. Fungal Diversity 63, 1–313 (2013). https://doi.org/10.1007/s13225-013-0263-4
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DOI: https://doi.org/10.1007/s13225-013-0263-4
Keywords
- Acrospermales
- Asterinales
- Botryosphaeriales
- Capnodiales
- Dothideales
- Dyfrolomycetales
- Hysteriales
- Jahnulales
- Lichenoconiales
- Lichenotheliales
- Microthyriales
- Monoblastiales
- Myriangiales
- Mytilinidiales
- Natipusillales
- Patellariales
- Phaeotrichales
- Phylogeny
- Pleosporales
- Strigulales
- Taxonomy
- Trypetheliales
- Tubeufiales
- Type species
- Venturiales