scispace - formally typeset
Search or ask a question
Author

Saowaluck Tibpromma

Bio: Saowaluck Tibpromma is an academic researcher from Kunming Institute of Botany. The author has contributed to research in topics: Biology & Phylogenetic tree. The author has an hindex of 21, co-authored 56 publications receiving 2687 citations. Previous affiliations of Saowaluck Tibpromma include Mae Fah Luang University & World Agroforestry Centre.

Papers published on a yearly basis

Papers
More filters
Journal ArticleDOI
TL;DR: Dothideomycetes comprise a highly diverse range of fungi characterized mainly by asci with two wall layers (bitunicate asci) and often with fissitunicate dehiscence, and it is hoped that by illustrating types they provide stimulation and interest so that more work is carried out in this remarkable group of fungi.
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.

501 citations

Journal ArticleDOI
Guo Jie Li1, Kevin D. Hyde2, Kevin D. Hyde3, Kevin D. Hyde4  +161 moreInstitutions (45)
TL;DR: This paper is a compilation of notes on 142 fungal taxa, including five new families, 20 new genera, and 100 new species, representing a wide taxonomic and geographic range.
Abstract: Notes on 113 fungal taxa are compiled in this paper, including 11 new genera, 89 new species, one new subspecies, three new combinations and seven reference specimens. A wide geographic and taxonomic range of fungal taxa are detailed. In the Ascomycota the new genera Angustospora (Testudinaceae), Camporesia (Xylariaceae), Clematidis, Crassiparies (Pleosporales genera incertae sedis), Farasanispora, Longiostiolum (Pleosporales genera incertae sedis), Multilocularia (Parabambusicolaceae), Neophaeocryptopus (Dothideaceae), Parameliola (Pleosporales genera incertae sedis), and Towyspora (Lentitheciaceae) are introduced. Newly introduced species are Angustospora nilensis, Aniptodera aquibella, Annulohypoxylon albidiscum, Astrocystis thailandica, Camporesia sambuci, Clematidis italica, Colletotrichum menispermi, C. quinquefoliae, Comoclathris pimpinellae, Crassiparies quadrisporus, Cytospora salicicola, Diatrype thailandica, Dothiorella rhamni, Durotheca macrostroma, Farasanispora avicenniae, Halorosellinia rhizophorae, Humicola koreana, Hypoxylon lilloi, Kirschsteiniothelia tectonae, Lindgomyces okinawaensis, Longiostiolum tectonae, Lophiostoma pseudoarmatisporum, Moelleriella phukhiaoensis, M. pongdueatensis, Mucoharknessia anthoxanthi, Multilocularia bambusae, Multiseptospora thysanolaenae, Neophaeocryptopus cytisi, Ocellularia arachchigei, O. ratnapurensis, Ochronectria thailandica, Ophiocordyceps karstii, Parameliola acaciae, P. dimocarpi, Parastagonospora cumpignensis, Pseudodidymosphaeria phlei, Polyplosphaeria thailandica, Pseudolachnella brevifusiformis, Psiloglonium macrosporum, Rhabdodiscus albodenticulatus, Rosellinia chiangmaiensis, Saccothecium rubi, Seimatosporium pseudocornii, S. pseudorosae, Sigarispora ononidis and Towyspora aestuari. New combinations are provided for Eutiarosporella dactylidis (sexual morph described and illustrated) and Pseudocamarosporium pini. Descriptions, illustrations and / or reference specimens are designated for Aposphaeria corallinolutea, Cryptovalsa ampelina, Dothiorella vidmadera, Ophiocordyceps formosana, Petrakia echinata, Phragmoporthe conformis and Pseudocamarosporium pini. The new species of Basidiomycota are Agaricus coccyginus, A. luteofibrillosus, Amanita atrobrunnea, A. digitosa, A. gleocystidiosa, A. pyriformis, A. strobilipes, Bondarzewia tibetica, Cortinarius albosericeus, C. badioflavidus, C. dentigratus, C. duboisensis, C. fragrantissimus, C. roseobasilis, C. vinaceobrunneus, C. vinaceogrisescens, C. wahkiacus, Cyanoboletus hymenoglutinosus, Fomitiporia atlantica, F. subtilissima, Ganoderma wuzhishanensis, Inonotus shoreicola, Lactifluus armeniacus, L. ramipilosus, Leccinum indoaurantiacum, Musumecia alpina, M. sardoa, Russula amethystina subp. tengii and R. wangii are introduced. Descriptions, illustrations, notes and / or reference specimens are designated for Clarkeinda trachodes, Dentocorticium ussuricum, Galzinia longibasidia, Lentinus stuppeus and Leptocorticium tenellum. The other new genera, species new combinations are Anaeromyces robustus, Neocallimastix californiae and Piromyces finnis from Neocallimastigomycota, Phytophthora estuarina, P. rhizophorae, Salispina, S. intermedia, S. lobata and S. spinosa from Oomycota, and Absidia stercoraria, Gongronella orasabula, Mortierella calciphila, Mucor caatinguensis, M. koreanus, M. merdicola and Rhizopus koreanus in Zygomycota.

488 citations

Journal ArticleDOI
TL;DR: This article provides an outline of the classification of the kingdom Fungi (including fossil fungi), and treats 19 phyla of fungi, including all currently described orders of fungi.
Abstract: This article provides an outline of the classification of the kingdom Fungi (including fossil fungi. i.e. dispersed spores, mycelia, sporophores, mycorrhizas). We treat 19 phyla of fungi. These are Aphelidiomycota, Ascomycota, Basidiobolomycota, Basidiomycota, Blastocladiomycota, Calcarisporiellomycota, Caulochytriomycota, Chytridiomycota, Entomophthoromycota, Entorrhizomycota, Glomeromycota, Kickxellomycota, Monoblepharomycota, Mortierellomycota, Mucoromycota, Neocallimastigomycota, Olpidiomycota, Rozellomycota and Zoopagomycota. The placement of all fungal genera is provided at the class-, order- and family-level. The described number of species per genus is also given. Notes are provided of taxa for which recent changes or disagreements have been presented. Fungus-like taxa that were traditionally treated as fungi are also incorporated in this outline (i.e. Eumycetozoa, Dictyosteliomycetes, Ceratiomyxomycetes and Myxomycetes). Four new taxa are introduced: Amblyosporida ord. nov. Neopereziida ord. nov. and Ovavesiculida ord. nov. in Rozellomycota, and Protosporangiaceae fam. nov. in Dictyosteliomycetes. Two different classifications (in outline section and in discussion) are provided for Glomeromycota and Leotiomycetes based on recent studies. The phylogenetic reconstruction of a four-gene dataset (18S and 28S rRNA, RPB1, RPB2) of 433 taxa is presented, including all currently described orders of fungi.

381 citations

Journal ArticleDOI
Jian-Kui Liu1, Kevin D. Hyde2, Kevin D. Hyde1, E. B. Gareth Jones3, Hiran A. Ariyawansa2, Hiran A. Ariyawansa1, Darbhe J. Bhat4, Saranyaphat Boonmee1, Sajeewa S. N. Maharachchikumbura2, Sajeewa S. N. Maharachchikumbura1, Eric H. C. McKenzie5, Rungtiwa Phookamsak2, Rungtiwa Phookamsak1, Chayanard Phukhamsakda1, Chayanard Phukhamsakda2, Belle Damodara Shenoy6, Mohamed A. Abdel-Wahab3, Mohamed A. Abdel-Wahab7, Bart Buyck, Jie Chen1, K. W. Thilini Chethana1, Chonticha Singtripop1, Chonticha Singtripop2, Dong-Qin Dai1, Dong-Qin Dai2, Yu Cheng Dai8, Dinushani A. Daranagama1, Dinushani A. Daranagama2, Asha J. Dissanayake1, Mingkwan Doilom2, Mingkwan Doilom1, Melvina J. D’souza2, Melvina J. D’souza1, Xinlei Fan8, Ishani D. Goonasekara1, Kazuyuki Hirayama, Sinang Hongsanan2, Sinang Hongsanan1, Subashini C. Jayasiri1, Ruvishika S. Jayawardena2, Ruvishika S. Jayawardena1, Samantha C. Karunarathna1, Samantha C. Karunarathna2, Wen-Jing Li1, Wen-Jing Li2, Ausana Mapook1, Ausana Mapook2, Chada Norphanphoun1, Ka-Lai Pang9, Rekhani H. Perera1, Rekhani H. Perera2, Derek Peršoh10, Umpava Pinruan11, Indunil C. Senanayake1, Indunil C. Senanayake2, Sayanh Somrithipol11, Satinee Suetrong11, Kazuaki Tanaka12, Kasun M. Thambugala2, Kasun M. Thambugala1, Qing Tian2, Qing Tian1, Saowaluck Tibpromma1, Danushka Udayanga1, Danushka Udayanga2, Nalin N. Wijayawardene1, Nalin N. Wijayawardene2, Nalin N. Wijayawardene13, Dhanuska Wanasinghe2, Dhanuska Wanasinghe1, Komsit Wisitrassameewong1, Xiang Yu Zeng1, Faten A. Abdel-Aziz7, Slavomír Adamčík14, Ali H. Bahkali3, Nattawut Boonyuen11, Timur S. Bulgakov15, Philippe Callac16, Putarak Chomnunti2, Putarak Chomnunti1, Katrin Greiner17, Akira Hashimoto18, Akira Hashimoto12, Valérie Hofstetter, Ji Chuan Kang13, David P. Lewis12, Xinghong Li, Xingzhong Liu, Zuo Yi Liu, Misato Matsumura12, Peter E. Mortimer2, Gerhard Rambold17, Emile Randrianjohany, Genki Sato12, Veera Sri-indrasutdhi11, Cheng Ming Tian8, Annemieke Verbeken19, Wolfgang von Brackel, Yong Wang13, Ting-Chi Wen13, Jianchu Xu2, Ji Ye Yan, Rui-Lin Zhao, Erio Camporesi 
TL;DR: This paper is a compilation of notes on 110 fungal taxa, including one new family, 10 new genera, and 76 new species, representing a wide taxonomic and geographic range.
Abstract: This paper is a compilation of notes on 110 fungal taxa, including one new family, 10 new genera, and 76 new species, representing a wide taxonomic and geographic range. The new family, Paradictyoarthriniaceae is introduced based on its distinct lineage in Dothideomycetes and its unique morphology. The family is sister to Biatriosporaceae and Roussoellaceae. The new genera are Allophaeosphaeria (Phaeosphaeriaceae), Amphibambusa (Amphisphaeriaceae), Brunneomycosphaerella (Capnodiales genera incertae cedis), Chaetocapnodium (Capnodiaceae), Flammeascoma (Anteagloniaceae), Multiseptospora (Pleosporales genera incertae cedis), Neogaeumannomyces (Magnaporthaceae), Palmiascoma (Bambusicolaceae), Paralecia (Squamarinaceae) and Sarimanas (Melanommataceae). The newly described species are the Ascomycota Aliquandostipite manochii, Allophaeosphaeria dactylidis, A. muriformia, Alternaria cesenica, Amphibambusa bambusicola, Amphisphaeria sorbi, Annulohypoxylon thailandicum, Atrotorquata spartii, Brunneomycosphaerella laburni, Byssosphaeria musae, Camarosporium aborescentis, C. aureum, C. frutexensis, Chaetocapnodium siamensis, Chaetothyrium agathis, Colletotrichum sedi, Conicomyces pseudotransvaalensis, Cytospora berberidis, C. sibiraeae, Diaporthe thunbergiicola, Diatrype palmicola, Dictyosporium aquaticum, D. meiosporum, D. thailandicum, Didymella cirsii, Dinemasporium nelloi, Flammeascoma bambusae, Kalmusia italica, K. spartii, Keissleriella sparticola, Lauriomyces synnematicus, Leptosphaeria ebuli, Lophiostoma pseudodictyosporium, L. ravennicum, Lophiotrema eburnoides, Montagnula graminicola, Multiseptospora thailandica, Myrothecium macrosporum, Natantispora unipolaris, Neogaeumannomyces bambusicola, Neosetophoma clematidis, N. italica, Oxydothis atypica, Palmiascoma gregariascomum, Paraconiothyrium nelloi, P. thysanolaenae, Paradictyoarthrinium tectonicola, Paralecia pratorum, Paraphaeosphaeria spartii, Pestalotiopsis digitalis, P. dracontomelon, P. italiana, Phaeoisaria pseudoclematidis, Phragmocapnias philippinensis, Pseudocamarosporium cotinae, Pseudocercospora tamarindi, Pseudotrichia rubriostiolata, P. thailandica, Psiloglonium multiseptatum, Saagaromyces mangrovei, Sarimanas pseudofluviatile, S. shirakamiense, Tothia spartii, Trichomerium siamensis, Wojnowicia dactylidicola, W. dactylidis and W. lonicerae. The Basidiomycota Agaricus flavicentrus, A. hanthanaensis, A. parvibicolor, A. sodalis, Cantharellus luteostipitatus, Lactarius atrobrunneus, L. politus, Phylloporia dependens and Russula cortinarioides are also introduced. Epitypifications or reference specimens are designated for Hapalocystis berkeleyi, Meliola tamarindi, Pallidocercospora acaciigena, Phaeosphaeria musae, Plenodomus agnitus, Psiloglonium colihuae, P. sasicola and Zasmidium musae while notes and/or new sequence data are provided for Annulohypoxylon leptascum, A. nitens, A. stygium, Biscogniauxia marginata, Fasciatispora nypae, Hypoxylon fendleri, H. monticulosum, Leptosphaeria doliolum, Microsphaeropsis olivacea, Neomicrothyrium, Paraleptosphaeria nitschkei, Phoma medicaginis and Saccotheciaceae. A full description of each species is provided with light micrographs (or drawings). Molecular data is provided for 90 taxa and used to generate phylogenetic trees to establish a natural classification for species.

304 citations

Journal ArticleDOI
Sergei Põlme1, Sergei Põlme2, Kessy Abarenkov1, R. Henrik Nilsson3, Björn D. Lindahl4, Karina E. Clemmensen4, Håvard Kauserud5, Nhu H. Nguyen6, Rasmus Kjøller7, Scott T. Bates8, Petr Baldrian9, Tobias Guldberg Frøslev7, Kristjan Adojaan2, Alfredo Vizzini10, Ave Suija2, Donald H. Pfister11, Hans Otto Baral, Helle Järv12, Hugo Madrid13, Hugo Madrid14, Jenni Nordén, Jian-Kui Liu15, Julia Pawłowska16, Kadri Põldmaa2, Kadri Pärtel2, Kadri Runnel2, Karen Hansen17, Karl-Henrik Larsson, Kevin D. Hyde18, Marcelo Sandoval-Denis, Matthew E. Smith19, Merje Toome-Heller20, Nalin N. Wijayawardene, Nelson Menolli21, Nicole K. Reynolds19, Rein Drenkhan22, Sajeewa S. N. Maharachchikumbura15, Tatiana Baptista Gibertoni23, Thomas Læssøe7, William J. Davis24, Yuri Tokarev, Adriana Corrales25, Adriene Mayra Soares, Ahto Agan2, A. R. Machado23, Andrés Argüelles-Moyao26, Andrew P. Detheridge, Angelina de Meiras-Ottoni23, Annemieke Verbeken27, Arun Kumar Dutta28, Bao-Kai Cui29, C. K. Pradeep, César Marín30, Daniel E. Stanton, Daniyal Gohar2, Dhanushka N. Wanasinghe31, Eveli Otsing2, Farzad Aslani2, Gareth W. Griffith, Thorsten Lumbsch32, Hans-Peter Grossart33, Hans-Peter Grossart34, Hossein Masigol35, Ina Timling36, Inga Hiiesalu2, Jane Oja2, John Y. Kupagme2, József Geml, Julieta Alvarez-Manjarrez26, Kai Ilves2, Kaire Loit22, Kalev Adamson22, Kazuhide Nara37, Kati Küngas2, Keilor Rojas-Jimenez38, Krišs Bitenieks39, Laszlo Irinyi40, Laszlo Irinyi41, Laszlo Nagy, Liina Soonvald22, Li-Wei Zhou31, Lysett Wagner34, M. Catherine Aime8, Maarja Öpik2, María Isabel Mujica30, Martin Metsoja2, Martin Ryberg42, Martti Vasar2, Masao Murata37, Matthew P. Nelsen32, Michelle Cleary4, Milan C. Samarakoon18, Mingkwan Doilom31, Mohammad Bahram2, Mohammad Bahram4, Niloufar Hagh-Doust2, Olesya Dulya2, Peter R. Johnston43, Petr Kohout9, Qian Chen31, Qing Tian18, Rajasree Nandi44, Rasekh Amiri2, Rekhani H. Perera18, Renata dos Santos Chikowski23, Renato Lucio Mendes-Alvarenga23, Roberto Garibay-Orijel26, Robin Gielen2, Rungtiwa Phookamsak31, Ruvishika S. Jayawardena18, Saleh Rahimlou2, Samantha C. Karunarathna31, Saowaluck Tibpromma31, Shawn P. Brown45, Siim-Kaarel Sepp2, Sunil Mundra46, Sunil Mundra5, Zhu Hua Luo47, Tanay Bose48, Tanel Vahter2, Tarquin Netherway4, Teng Yang31, Tom W. May49, Torda Varga, Wei Li50, Victor R. M. Coimbra23, Virton Rodrigo Targino de Oliveira23, Vitor Xavier de Lima23, Vladimir S. Mikryukov2, Yong-Zhong Lu51, Yosuke Matsuda52, Yumiko Miyamoto53, Urmas Kõljalg1, Urmas Kõljalg2, Leho Tedersoo2, Leho Tedersoo1 
American Museum of Natural History1, University of Tartu2, University of Gothenburg3, Swedish University of Agricultural Sciences4, University of Oslo5, University of Hawaii at Manoa6, University of Copenhagen7, Purdue University8, Academy of Sciences of the Czech Republic9, University of Turin10, Harvard University11, Synlab Group12, Universidad Santo Tomás13, Universidad Mayor14, University of Electronic Science and Technology of China15, University of Warsaw16, Swedish Museum of Natural History17, Mae Fah Luang University18, University of Florida19, Laos Ministry of Agriculture and Forestry20, São Paulo Federal Institute of Education, Science and Technology21, Estonian University of Life Sciences22, Federal University of Pernambuco23, United States Department of Energy24, Del Rosario University25, National Autonomous University of Mexico26, Ghent University27, West Bengal State University28, Beijing Forestry University29, Pontifical Catholic University of Chile30, Chinese Academy of Sciences31, Field Museum of Natural History32, University of Potsdam33, Leibniz Association34, University of Gilan35, University of Alaska Fairbanks36, University of Tokyo37, University of Costa Rica38, Forest Research Institute39, Westmead Hospital40, University of Sydney41, Uppsala University42, Landcare Research43, University of Chittagong44, University of Memphis45, United Arab Emirates University46, Ministry of Land and Resources of the People's Republic of China47, University of Pretoria48, Royal Botanic Gardens49, Ocean University of China50, Guizhou University51, Mie University52, Hokkaido University53
TL;DR: Fungal traits and character database FungalTraits operating at genus and species hypothesis levels is presented in this article, which includes 17 lifestyle related traits of fungal and Stramenopila genera.
Abstract: The cryptic lifestyle of most fungi necessitates molecular identification of the guild in environmental studies. Over the past decades, rapid development and affordability of molecular tools have tremendously improved insights of the fungal diversity in all ecosystems and habitats. Yet, in spite of the progress of molecular methods, knowledge about functional properties of the fungal taxa is vague and interpretation of environmental studies in an ecologically meaningful manner remains challenging. In order to facilitate functional assignments and ecological interpretation of environmental studies we introduce a user friendly traits and character database FungalTraits operating at genus and species hypothesis levels. Combining the information from previous efforts such as FUNGuild and Fun(Fun) together with involvement of expert knowledge, we reannotated 10,210 and 151 fungal and Stramenopila genera, respectively. This resulted in a stand-alone spreadsheet dataset covering 17 lifestyle related traits of fungal and Stramenopila genera, designed for rapid functional assignments of environmental studies. In order to assign the trait states to fungal species hypotheses, the scientific community of experts manually categorised and assigned available trait information to 697,413 fungal ITS sequences. On the basis of those sequences we were able to summarise trait and host information into 92,623 fungal species hypotheses at 1% dissimilarity threshold.

245 citations


Cited by
More filters
01 Jan 1944
TL;DR: The only previously known species of Myrsidea from bulbuls, M. warwicki ex Ixos philippinus, is redescribed and sixteen new species are described; they and their type hosts are described.
Abstract: We redescribe the only previously known species of Myrsidea from bulbuls, M. pycnonoti Eichler. Sixteen new species are described; they and their type hosts are: M. phillipsi ex Pycnonotus goiavier goiavier (Scopoli), M. gieferi ex P. goiavier suluensis Mearns, M. kulpai ex P. flavescens Blyth, M. finlaysoni ex P. finlaysoni Strickland, M. kathleenae ex P. cafer (L.), M. warwicki ex Ixos philippinus (J. R. Forster), M. mcclurei ex Microscelis amaurotis (Temminck), M. zeylanici ex P. zeylanicus (Gmelin), M. plumosi ex P. plumosus Blyth, M. eutiloti ex P. eutilotus (Jardine and Selby), M. adamsae ex P. urostictus (Salvadori), M. ochracei ex Criniger ochraceus F. Moore, M. borbonici ex Hypsipetes borbonicus (J. R. Forster), M. johnsoni ex P. atriceps (Temminck), M. palmai ex C. ochraceus, and M. claytoni ex P. eutilotus. A key is provided for the identification of these 17 species.

1,756 citations

Journal ArticleDOI

559 citations

Journal ArticleDOI
01 Sep 1926-Nature
TL;DR: The Washington Biological Society has just published a reprint at the price of one dollar of the Code ofworms, with the permission of the Commission.
Abstract: DURING this year I have so often been asked how this Code could be obtained that I hasten, with your permission, to announce that the Washington Biological Society has just published a reprint at the price of one dollar. Prof. C. W. Stiles, secretary to the Commission, says: “I would suggest that, if your colleagues wish copies, it would expedite matters to order a number at once”. The address of the Society is at the Bureau of Entomology, Washington, D.C., U.S.A.

525 citations

Journal ArticleDOI
Guo Jie Li1, Kevin D. Hyde2, Kevin D. Hyde3, Kevin D. Hyde4  +161 moreInstitutions (45)
TL;DR: This paper is a compilation of notes on 142 fungal taxa, including five new families, 20 new genera, and 100 new species, representing a wide taxonomic and geographic range.
Abstract: Notes on 113 fungal taxa are compiled in this paper, including 11 new genera, 89 new species, one new subspecies, three new combinations and seven reference specimens. A wide geographic and taxonomic range of fungal taxa are detailed. In the Ascomycota the new genera Angustospora (Testudinaceae), Camporesia (Xylariaceae), Clematidis, Crassiparies (Pleosporales genera incertae sedis), Farasanispora, Longiostiolum (Pleosporales genera incertae sedis), Multilocularia (Parabambusicolaceae), Neophaeocryptopus (Dothideaceae), Parameliola (Pleosporales genera incertae sedis), and Towyspora (Lentitheciaceae) are introduced. Newly introduced species are Angustospora nilensis, Aniptodera aquibella, Annulohypoxylon albidiscum, Astrocystis thailandica, Camporesia sambuci, Clematidis italica, Colletotrichum menispermi, C. quinquefoliae, Comoclathris pimpinellae, Crassiparies quadrisporus, Cytospora salicicola, Diatrype thailandica, Dothiorella rhamni, Durotheca macrostroma, Farasanispora avicenniae, Halorosellinia rhizophorae, Humicola koreana, Hypoxylon lilloi, Kirschsteiniothelia tectonae, Lindgomyces okinawaensis, Longiostiolum tectonae, Lophiostoma pseudoarmatisporum, Moelleriella phukhiaoensis, M. pongdueatensis, Mucoharknessia anthoxanthi, Multilocularia bambusae, Multiseptospora thysanolaenae, Neophaeocryptopus cytisi, Ocellularia arachchigei, O. ratnapurensis, Ochronectria thailandica, Ophiocordyceps karstii, Parameliola acaciae, P. dimocarpi, Parastagonospora cumpignensis, Pseudodidymosphaeria phlei, Polyplosphaeria thailandica, Pseudolachnella brevifusiformis, Psiloglonium macrosporum, Rhabdodiscus albodenticulatus, Rosellinia chiangmaiensis, Saccothecium rubi, Seimatosporium pseudocornii, S. pseudorosae, Sigarispora ononidis and Towyspora aestuari. New combinations are provided for Eutiarosporella dactylidis (sexual morph described and illustrated) and Pseudocamarosporium pini. Descriptions, illustrations and / or reference specimens are designated for Aposphaeria corallinolutea, Cryptovalsa ampelina, Dothiorella vidmadera, Ophiocordyceps formosana, Petrakia echinata, Phragmoporthe conformis and Pseudocamarosporium pini. The new species of Basidiomycota are Agaricus coccyginus, A. luteofibrillosus, Amanita atrobrunnea, A. digitosa, A. gleocystidiosa, A. pyriformis, A. strobilipes, Bondarzewia tibetica, Cortinarius albosericeus, C. badioflavidus, C. dentigratus, C. duboisensis, C. fragrantissimus, C. roseobasilis, C. vinaceobrunneus, C. vinaceogrisescens, C. wahkiacus, Cyanoboletus hymenoglutinosus, Fomitiporia atlantica, F. subtilissima, Ganoderma wuzhishanensis, Inonotus shoreicola, Lactifluus armeniacus, L. ramipilosus, Leccinum indoaurantiacum, Musumecia alpina, M. sardoa, Russula amethystina subp. tengii and R. wangii are introduced. Descriptions, illustrations, notes and / or reference specimens are designated for Clarkeinda trachodes, Dentocorticium ussuricum, Galzinia longibasidia, Lentinus stuppeus and Leptocorticium tenellum. The other new genera, species new combinations are Anaeromyces robustus, Neocallimastix californiae and Piromyces finnis from Neocallimastigomycota, Phytophthora estuarina, P. rhizophorae, Salispina, S. intermedia, S. lobata and S. spinosa from Oomycota, and Absidia stercoraria, Gongronella orasabula, Mortierella calciphila, Mucor caatinguensis, M. koreanus, M. merdicola and Rhizopus koreanus in Zygomycota.

488 citations

Journal ArticleDOI
TL;DR: The present paper introduces the FoF database to the scientific community and briefly reviews some of the problems associated with classification and identification of the main fungal groups.
Abstract: Taxonomic names are key links between various databases that store information on different organisms. Several global fungal nomenclural and taxonomic databases (notably Index Fungorum, Species Fungorum and MycoBank) can be sourced to find taxonomic details about fungi, while DNA sequence data can be sourced from NCBI, EBI and UNITE databases. Although the sequence data may be linked to a name, the quality of the metadata is variable and generally there is no corresponding link to images, descriptions or herbarium material. There is generally no way to establish the accuracy of the names in these genomic databases, other than whether the submission is from a reputable source. To tackle this problem, a new database (FacesofFungi), accessible at www.facesoffungi.org (FoF) has been established. This fungal database allows deposition of taxonomic data, phenotypic details and other useful data, which will enhance our current taxonomic understanding and ultimately enable mycologists to gain better and updated insights into the current fungal classification system. In addition, the database will also allow access to comprehensive metadata including descriptions of voucher and type specimens. This database is user-friendly, providing links and easy access between taxonomic ranks, with the classification system based primarily on molecular data (from the literature and via updated web-based phylogenetic trees), and to a lesser extent on morphological data when molecular data are unavailable. In FoF species are not only linked to the closest phylogenetic representatives, but also relevant data is provided, wherever available, on various applied aspects, such as ecological, industrial, quarantine and chemical uses. The data include the three main fungal groups (Ascomycota, Basidiomycota, Basal fungi) and fungus-like organisms. The FoF webpage is an output funded by the Mushroom Research Foundation which is an NGO with seven directors with mycological expertise. The webpage has 76 curators, and with the help of these specialists, FoF will provide an updated natural classification of the fungi, with illustrated accounts of species linked to molecular data. The present paper introduces the FoF database to the scientific community and briefly reviews some of the problems associated with classification and identification of the main fungal groups. The structure and use of the database is then explained. We would like to invite all mycologists to contribute to these web pages.

458 citations