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. 2021 Jun:46:313-528.
doi: 10.3767/persoonia.2021.46.11. Epub 2021 Jul 13.

Fungal Planet description sheets: 1182-1283

P W Crous  1   2 , D A Cowan  3 , G Maggs-Kölling  4 , N Yilmaz  2 , R Thangavel  5 , M J Wingfield  2 , M E Noordeloos  6 , B Dima  7 , T E Brandrud  8 , G M Jansen  9 , O V Morozova  10 , J Vila  11 , R G Shivas  12 , Y P Tan  13 , S Bishop-Hurley  13 , E Lacey  14 , T S Marney  13 , E Larsson  15 , G Le Floch  16 , L Lombard  1 , P Nodet  16 , V Hubka  17   18 , P Alvarado  19 , A Berraf-Tebbal  20 , J D Reyes  21 , G Delgado  22 , A Eichmeier  20 , J B Jordal  23 , A V Kachalkin  24   25 , A Kubátová  17 , J G Maciá-Vicente  26 , E F Malysheva  10 , V Papp  27 , K C Rajeshkumar  28 , A Sharma  12 , M Spetik  20 , D Szabóová  29 , M A Tomashevskaya  25 , J A Abad  30 , Z G Abad  30 , A V Alexandrova  24   31 , G Anand  32 , F Arenas  33 , N Ashtekar  28 , S Balashov  34 , Á Bañares  35 , R Baroncelli  36 , I Bera  37 , A Yu Biketova  38 , C L Blomquist  39 , T Boekhout  1 , D Boertmann  40 , T M Bulyonkova  41 , T I Burgess  42 , A J Carnegie  43 , J F Cobo-Diaz  16 , G Corriol  44 , J H Cunnington  45 , M O da Cruz  46 , U Damm  47 , N Davoodian  48 , A L C M de A Santiago  46 , J Dearnaley  12 , L W S de Freitas  46 , K Dhileepan  49 , R Dimitrov  50 , S Di Piazza  51 , S Fatima  28 , F Fuljer  52 , H Galera  53 , A Ghosh  54 , A Giraldo  55 , A M Glushakova  24   56 , M Gorczak  57   58 , D E Gouliamova  50 , D Gramaje  59 , M Groenewald  1 , C K Gunsch  60 , A Gutiérrez  33 , D Holdom  49 , J Houbraken  1 , A B Ismailov  61 , Ł Istel  1   57 , T Iturriaga  62 , M Jeppson  15 , Ž Jurjević  34 , L B Kalinina  10 , V I Kapitonov  63 , I Kautmanová  29 , A N Khalid  64 , M Kiran  64 , L Kiss  12 , Á Kovács  38 , D Kurose  65 , I Kušan  66 , S Lad  28 , T Læssøe  67 , H B Lee  68 , J J Luangsa-Ard  69 , M Lynch  12 , A E Mahamedi  70 , V F Malysheva  10 , A Mateos  71 , N Matočec  66 , A Mešić  66 , A N Miller  72 , S Mongkolsamrit  69 , G Moreno  73 , A Morte  33 , R Mostowfizadeh-Ghalamfarsa  74 , A Naseer  64 , A Navarro-Ródenas  33 , T T T Nguyen  68 , W Noisripoom  69 , J E Ntandu  75 , J Nuytinck  6   76 , V Ostrý  77 , T A Pankratov  78 , J Pawłowska  57 , J Pecenka  20 , T H G Pham  31 , A Polhorský  79 , A Pošta  66 , D B Raudabaugh  60 , K Reschke  80 , A Rodríguez  33 , M Romero  81 , S Rooney-Latham  39 , J Roux  82 , M Sandoval-Denis  1 , M Th Smith  1 , T V Steinrucken  83 , T Y Svetasheva  84 , Z Tkalčec  66 , E J van der Linde  85 , M V D Vegte  86 , J Vauras  87 , A Verbeken  76 , C M Visagie  2 , J S Vitelli  49 , S V Volobuev  10 , A Weill  88 , M Wrzosek  58 , I V Zmitrovich  10 , E A Zvyagina  24 , J Z Groenewald  1
Affiliations

Fungal Planet description sheets: 1182-1283

P W Crous et al. Persoonia. 2021 Jun.

Abstract

Novel species of fungi described in this study include those from various countries as follows: Algeria, Phaeoacremonium adelophialidum from Vitis vinifera. Antarctica, Comoclathris antarctica from soil. Australia, Coniochaeta salicifolia as endophyte from healthy leaves of Geijera salicifolia, Eremothecium peggii in fruit of Citrus australis, Microdochium ratticaudae from stem of Sporobolus natalensis, Neocelosporium corymbiae on stems of Corymbia variegata, Phytophthora kelmanii from rhizosphere soil of Ptilotus pyramidatus, Pseudosydowia backhousiae on living leaves of Backhousia citriodora, Pseudosydowia indooroopillyensis, Pseudosydowia louisecottisiae and Pseudosydowia queenslandica on living leaves of Eucalyptus sp. Brazil, Absidia montepascoalis from soil. Chile, Ilyonectria zarorii from soil under Maytenus boaria. Costa Rica, Colletotrichum filicis from an unidentified fern. Croatia, Mollisia endogranulata on deteriorated hardwood. Czech Republic, Arcopilus navicularis from tea bag with fruit tea, Neosetophoma buxi as endophyte from Buxus sempervirens, Xerochrysium bohemicum on surface of biscuits with chocolate glaze and filled with jam. France, Entoloma cyaneobasale on basic to calcareous soil, Fusarium aconidiale from Triticum aestivum, Fusarium juglandicola from buds of Juglans regia. Germany, Tetraploa endophytica as endophyte from Microthlaspi perfoliatum roots. India, Castanediella ambae on leaves of Mangifera indica, Lactifluus kanadii on soil under Castanopsis sp., Penicillium uttarakhandense from soil. Italy, Penicillium ferraniaense from compost. Namibia, Bezerromyces gobabebensis on leaves of unidentified succulent, Cladosporium stipagrostidicola on leaves of Stipagrostis sp., Cymostachys euphorbiae on leaves of Euphorbia sp., Deniquelata hypolithi from hypolith under a rock, Hysterobrevium walvisbayicola on leaves of unidentified tree, Knufia hypolithi and Knufia walvisbayicola from hypolith under a rock, Lapidomyces stipagrostidicola on leaves of Stipagrostis sp., Nothophaeotheca mirabibensis (incl. Nothophaeotheca gen. nov.) on persistent inflorescence remains of Blepharis obmitrata, Paramyrothecium salvadorae on twigs of Salvadora persica, Preussia procaviicola on dung of Procavia sp., Sordaria equicola on zebra dung, Volutella salvadorae on stems of Salvadora persica. Netherlands, Entoloma ammophilum on sandy soil, Entoloma pseudocruentatum on nutrient poor (acid) soil, Entoloma pudens on plant debris, amongst grasses. New Zealand, Amorocoelophoma neoregeliae from leaf spots of Neoregelia sp., Aquilomyces metrosideri and Septoriella callistemonis from stem discolouration and leaf spots of Metrosideros sp., Cadophora neoregeliae from leaf spots of Neoregelia sp., Flexuomyces asteliae (incl. Flexuomyces gen. nov.) and Mollisia asteliae from leaf spots of Astelia chathamica, Ophioceras freycinetiae from leaf spots of Freycinetia banksii, Phaeosphaeria caricis-sectae from leaf spots of Carex secta. Norway, Cuphophyllus flavipesoides on soil in semi-natural grassland, Entoloma coracis on soil in calcareous Pinus and Tilia forests, Entoloma cyaneolilacinum on soil semi-natural grasslands, Inocybe norvegica on gravelly soil. Pakistan, Butyriboletus parachinarensis on soil in association with Quercus baloot. Poland, Hyalodendriella bialowiezensis on debris beneath fallen bark of Norway spruce Picea abies. Russia, Bolbitius sibiricus on à moss covered rotting trunk of Populus tremula, Crepidotus wasseri on debris of Populus tremula, Entoloma isborscanum on soil on calcareous grasslands, Entoloma subcoracis on soil in subalpine grasslands, Hydropus lecythiocystis on rotted wood of Betula pendula, Meruliopsis faginea on fallen dead branches of Fagus orientalis, Metschnikowia taurica from fruits of Ziziphus jujube, Suillus praetermissus on soil, Teunia lichenophila as endophyte from Cladonia rangiferina. Slovakia, Hygrocybe fulgens on mowed grassland, Pleuroflammula pannonica from corticated branches of Quercus sp. South Africa, Acrodontium burrowsianum on leaves of unidentified Poaceae, Castanediella senegaliae on dead pods of Senegalia ataxacantha, Cladophialophora behniae on leaves of Behnia sp., Colletotrichum cliviigenum on leaves of Clivia sp., Diatrype dalbergiae on bark of Dalbergia armata, Falcocladium heteropyxidicola on leaves of Heteropyxis canescens, Lapidomyces aloidendricola as epiphyte on brown stem of Aloidendron dichotomum, Lasionectria sansevieriae and Phaeosphaeriopsis sansevieriae on leaves of Sansevieria hyacinthoides, Lylea dalbergiae on Diatrype dalbergiae on bark of Dalbergia armata, Neochaetothyrina syzygii (incl. Neochaetothyrina gen. nov.) on leaves of Syzygium chordatum, Nothophaeomoniella ekebergiae (incl. Nothophaeomoniella gen. nov.) on leaves of Ekebergia pterophylla, Paracymostachys euphorbiae (incl. Paracymostachys gen. nov.) on leaf litter of Euphorbia ingens, Paramycosphaerella pterocarpi on leaves of Pterocarpus angolensis, Paramycosphaerella syzygii on leaf litter of Syzygium chordatum, Parateichospora phoenicicola (incl. Parateichospora gen. nov.) on leaves of Phoenix reclinata, Seiridium syzygii on twigs of Syzygium chordatum, Setophoma syzygii on leaves of Syzygium sp., Starmerella xylocopis from larval feed of an Afrotropical bee Xylocopa caffra, Teratosphaeria combreti on leaf litter of Combretum kraussii, Teratosphaericola leucadendri on leaves of Leucadendron sp., Toxicocladosporium pterocarpi on pods of Pterocarpus angolensis. Spain, Cortinarius bonachei with Quercus ilex in calcareus soils, Cortinarius brunneovolvatus under Quercus ilex subsp. ballota in calcareous soil, Extremopsis radicicola (incl. Extremopsis gen. nov.) from root-associated soil in a wet heathland, Russula quintanensis on acidic soils, Tubaria vulcanica on volcanic lapilii material, Tuber zambonelliae in calcareus soil. Sweden, Elaphomyces borealis on soil under Pinus sylvestris and Betula pubescens. Tanzania, Curvularia tanzanica on inflorescence of Cyperus aromaticus. Thailand, Simplicillium niveum on Ophiocordyceps camponoti-leonardi on underside of unidentified dicotyledonous leaf. USA, Calonectria californiensis on leaves of Umbellularia californica, Exophiala spartinae from surface sterilised roots of Spartina alterniflora, Neophaeococcomyces oklahomaensis from outside wall of alcohol distillery. Vietnam, Fistulinella aurantioflava on soil. Morphological and culture characteristics are supported by DNA barcodes. Citation: Crous PW, Cowan DA, Maggs-Kölling, et al. 2021. Fungal Planet description sheets: 1182-1283. Persoonia 46: 313-528. https://doi.org/10.3767/persoonia.2021.46.11.

Keywords: ITS nrDNA barcodes; LSU; new taxa; systematics.

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Figures

None
Overview Agaricomycetes phylogeny
Consensus phylogram (50 % majority rule) of 279 752 trees resulting from a Bayesian analysis of the LSU sequence alignment (170 sequences including outgroup; 948 aligned positions; 553 unique site patterns; 1 865 000 generations with trees sampled every 10 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families, orders and classes are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Backusella lamprospora (GenBank MH866118.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Agaricomycetes phylogeny
Consensus phylogram (50 % majority rule) of 279 752 trees resulting from a Bayesian analysis of the LSU sequence alignment (170 sequences including outgroup; 948 aligned positions; 553 unique site patterns; 1 865 000 generations with trees sampled every 10 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families, orders and classes are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Backusella lamprospora (GenBank MH866118.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Agaricomycetes phylogeny
Consensus phylogram (50 % majority rule) of 279 752 trees resulting from a Bayesian analysis of the LSU sequence alignment (170 sequences including outgroup; 948 aligned positions; 553 unique site patterns; 1 865 000 generations with trees sampled every 10 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families, orders and classes are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Backusella lamprospora (GenBank MH866118.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Dothideomycetes (Other orders) phylogeny
Consensus phylogram (50 % majority rule) of 56 102 trees resulting from a Bayesian analysis of the LSU sequence alignment (179 sequences including outgroup; 832 aligned positions; 378 unique site patterns; 3 740 000 generations with trees sampled every 100 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Diaporthe perjuncta (GenBank NG_059064.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The most basal branched was halved in length to facilitate layout. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Dothideomycetes (Other orders) phylogeny
Consensus phylogram (50 % majority rule) of 56 102 trees resulting from a Bayesian analysis of the LSU sequence alignment (179 sequences including outgroup; 832 aligned positions; 378 unique site patterns; 3 740 000 generations with trees sampled every 100 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Diaporthe perjuncta (GenBank NG_059064.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The most basal branched was halved in length to facilitate layout. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Dothideomycetes (Pleosporales) phylogeny
Consensus phylogram (50 % majority rule) of 91 128 trees resulting from a Bayesian analysis of the LSU sequence alignment (170 sequences including outgroup; 799 aligned positions; 295 unique site patterns; 6 075 000 generations with trees sampled every 100 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Diaporthe perjuncta (GenBank NG_059064.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Dothideomycetes (Pleosporales) phylogeny
Consensus phylogram (50 % majority rule) of 91 128 trees resulting from a Bayesian analysis of the LSU sequence alignment (170 sequences including outgroup; 799 aligned positions; 295 unique site patterns; 6 075 000 generations with trees sampled every 100 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Diaporthe perjuncta (GenBank NG_059064.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Eurotiomycetes phylogeny
Consensus phylogram (50 % majority rule) of 146 252 trees resulting from a Bayesian analysis of the LSU sequence alignment (85 sequences including outgroup; 847 aligned positions; 357 unique site patterns; 1 010 000 generations with trees sampled every 10 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Diaporthe perjuncta (GenBank NG_059064.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Eurotiomycetes phylogeny
Consensus phylogram (50 % majority rule) of 146 252 trees resulting from a Bayesian analysis of the LSU sequence alignment (85 sequences including outgroup; 847 aligned positions; 357 unique site patterns; 1 010 000 generations with trees sampled every 10 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Diaporthe perjuncta (GenBank NG_059064.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Leotiomycetes phylogeny
Consensus phylogram (50 % majority rule) of 408 002 trees resulting from a Bayesian analysis of the LSU sequence alignment (90 sequences including outgroup; 826 aligned positions; 283 unique site patterns; 2 720 000 generations with trees sampled every 10 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Xylaria hypoxylon (GenBank AY544648.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The most basal branched was halved in length to facilitate layout. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Mucoromycetes phylogeny
Consensus phylogram (50 % majority rule) of 141 002 trees resulting from a Bayesian analysis of the LSU sequence alignment (22 sequences including outgroup; 660 aligned positions; 319 unique site patterns; 470 000 generations with trees sampled every five generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. The higher taxonomic classification is indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Chytridium lagenaria (GenBank FJ804156.1) and the taxonomic novelty described in this study for which LSU sequence data were available is indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Pezizomycetes phylogeny
Consensus phylogram (50 % majority rule) of 87 002 trees resulting from a Bayesian analysis of the LSU sequence alignment (33 sequences including outgroup; 792 aligned positions; 203 unique site patterns; 290 000 generations with trees sampled every five generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. The family and order are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Candida broadrunensis (GenBank KY106372.1) and the taxonomic novelty described in this study for which LSU sequence data were available is indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Phytophthora phylogeny
Consensus phylogram (50 % majority rule) of 64 502 trees resulting from a Bayesian analysis of the LSU sequence alignment (25 sequences including outgroup; 1 110 aligned positions; 68 unique site patterns; 215 000 generations with trees sampled every five generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. The higher taxonomic classification is indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Absidia panacisoli (GenBank NG_063948.1) and the taxonomic novelty described in this study for which LSU sequence data were available is indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Saccharomycetes and Tremellomycetes phylogeny
Consensus phylogram (50 % majority rule) of 136 502 trees resulting from a Bayesian analysis of the LSU sequence alignment (36 sequences including outgroup; 667 aligned positions; 432 unique site patterns; 910 000 generations with trees sampled every 10 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. The families, orders and classes are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Backusella lamprospora (GenBank MH866118.1) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Sordariomycetes (Falcocladiales, Glomerellales and Hypocreales) phylogeny
Consensus phylogram (50 % majority rule) of 846 978 trees resulting from a Bayesian analysis of the LSU sequence alignment (194 sequences including outgroup; 816 aligned positions; 310 unique site patterns; 56 465 000 generations with trees sampled every 100 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Ramularia endophylla (GenBank AY490776.2) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Sordariomycetes (Falcocladiales, Glomerellales and Hypocreales) phylogeny
Consensus phylogram (50 % majority rule) of 846 978 trees resulting from a Bayesian analysis of the LSU sequence alignment (194 sequences including outgroup; 816 aligned positions; 310 unique site patterns; 56 465 000 generations with trees sampled every 100 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Ramularia endophylla (GenBank AY490776.2) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Sordariomycetes (Falcocladiales, Glomerellales and Hypocreales) phylogeny
Consensus phylogram (50 % majority rule) of 846 978 trees resulting from a Bayesian analysis of the LSU sequence alignment (194 sequences including outgroup; 816 aligned positions; 310 unique site patterns; 56 465 000 generations with trees sampled every 100 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Ramularia endophylla (GenBank AY490776.2) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Sordariomycetes (Other orders) phylogeny
Consensus phylogram (50 % majority rule) of 229 502 trees resulting from a Bayesian analysis of the LSU sequence alignment (79 sequences including outgroup; 813 aligned positions; 293 unique site patterns; 1 530 000 generations with trees sampled every 10 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and orders are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Ramularia endophylla (GenBank AY490776.2) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Overview Sordariomycetes (Xylariales) phylogeny
Consensus phylogram (50 % majority rule) of 118 502 trees resulting from a Bayesian analysis of the LSU sequence alignment (63 sequences including outgroup; 800 aligned positions; 192 unique site patterns; 790 000 generations with trees sampled every 10 generations) using MrBayes v. 3.2.7a (Ronquist et al. 2012). Bayesian posterior probabilities (PP) > 0.84 are shown at the nodes and thickened lines represent nodes with PP = 1.00. The scale bar represents the expected changes per site. Families and the order are indicated with coloured blocks to the right of the tree. Culture collection/voucher, GenBank accession (in superscript) and/or Fungal Planet numbers are indicated behind the species names. The tree was rooted to Ramularia endophylla (GenBank AY490776.2) and the taxonomic novelties described in this study for which LSU sequence data were available are indicated in bold face. The most basal branched was halved in length to facilitate layout. The alignment and tree were deposited in TreeBASE (Submission ID 28129).
None
Ophioceras freycinetiae
None
Mollisia asteliae & Flexuomyces asteliae
None
Amorocoelophoma neoregeliae & Cadophora neoregeliae
None
Septoriella callistemonis
None
Phaeosphaeria caricis-sectae
None
Cladophialophora behniae
None
Colletotrichum cliviigenum
None
Aquilomyces metrosideri
None
Falcocladium heteropyxidicola & Castanediella senegaliae
None
Paracymostachys euphorbiae
None
Cladosporium stipagrostidicola
None
Teratosphaericola leucadendri
None
Toxicocladosporium pterocarpi
None
Diatrype dalbergiae & Lylea dalbergiae
None
Acrodontium burrowsianum
None
Bezerromyces gobabebensis
None
Lapidomyces stipagrostidicola
None
Hysterobrevium walvisbayicola
None
Deniquelata hypolithi
None
Knufia hypolithi
None
Knufia walvisbayicola
None
Sordaria equicola
None
Lapidomyces aloidendricola
None
Phaeosphaeriopsis sansevieriae & Lasionectria sansevieriae
None
Nothophaeotheca mirabibensis
None
Preussia procaviicola
None
Teratosphaeria combreti
None
Neochaetothyrina syzygii
None
Seiridium syzygii
None
Setophoma syzygii
None
Paramycosphaerella syzygii
None
Paramycosphaerella pterocarpi
None
Volutella salvadorae
None
Neocelosporium corymbiae
None
Paramyrothecium salvadorae
None
Cymostachys arthraeruae
None
Parateichospora phoenicicola
None
Nothophaeomoniella ekebergiae
None
Calonectria californiensis
None
Absidia montepascoalis
None
Arcopilus navicularis
None
Bolbitius sibiricus
None
Butyriboletus parachinarensis
None
Castanediella ambae
None
Colletotrichum filicis
None
Comoclathris antarctica
None
Coniochaeta salicifolia
None
Cortianarius bonachei
None
Cortinarius brunneovolvatus
None
Crepidotus wasseri
None
Cuphophyllus flavipesoides
None
Curvularia tanzanica
None
Elaphomyces borealis
None
Entoloma ammophilum
None
Entoloma coracis
None
Entoloma cyaneobasale
None
Entoloma cyaneolilacinum
None
Entoloma isborscanum
None
Entoloma pseudocruentatum
None
Entoloma pudens
None
Entoloma subcoracis
None
Eremothecium peggii
None
Exophiala spartinae
None
Extremopsis radicicola
None
Fistulinella aurantioflava
None
Hyalodendriella bialowiezensis
None
Hydropus lecythiocystis
None
Hygrocybe fulgens
None
Ilyonectria zarorii
None
Inocybe norvegica
None
Lactifluus kanadii
None
Meruliopsis faginea
None
Metschnikowia taurica
None
Microdochium ratticaudae
None
Mollisia endogranulata
None
Neophaeococcomyces oklahomaensis
None
Neosetophoma buxi
None
Penicillium ferraniaense
None
Penicillium uttarakhandense
None
Phaeoacremonium adelophialidum
None
Phytophthora kelmanii
None
Pleuroflammula pannonica
None
Pseudosydowia backhousiae, Pseudosydowia indooroopillyensis, Pseudosydowia louisecottisiae & Pseudosydowia queenslandica
None
Russula quintanensis
None
Simplicillium niveum
None
Starmerella xylocopis
None
Suillus praetermissus
None
Tetraploa endophytica
None
Teunia lichenophila
None
Tubaria vulcanica
None
Tuber zambonelliae
None
Xerochrysium bohemicum
None
Fusarium juglandicola
None
Fusarium aconidiale
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
None
See this image and copyright information in PMC

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