Abstract
Ascomycota, the most speciose phylum of fungi, is a complex entity, comprising three diverse subphyla: Pezizomycotina, Saccharomycotina, and Taphrinomycotina. The largest and most diverse subphylum, Pezizomycotina, is a rich tapestry of 16 classes and 171 orders. Saccharomycotina, the second largest subphylum, is a diverse collection of seven classes and 12 orders, while Taphrinomycotina, the smallest, is a unique assembly of six classes and six orders. Over the past decade, numerous taxonomic studies have focused on the generic, family, and class classifications of Ascomycota. These efforts, well-documented across various databases, are crucial for a comprehensive understanding of the classification. However, the study of taxonomy at the ordinal level, a crucial tier in the taxonomic hierarchy, has been largely overlooked. In a global collaboration with mycologists and lichenologists, this study presents the first comprehensive information on the orders within Pezizomycotina and Taphrinomycotina. The recent taxonomic classification of Saccharomycotina has led to the exclusion of this subphylum from the present study, as an immediate revision is not necessary. Each order is thoroughly discussed, highlighting its historical significance, current status, key identification characteristics, evolutionary relationships, ecological and economic roles, future recommendations, and updated family-level classification. Teaching diagrams for the life cycles of several orders, viz. Asterinales, Helotiales, Hypocreales, Laboulbeniales, Meliolales, Mycosphaerellales, Ophiostomatales, Pezizales, Pleosporales, Phyllachorales, Rhytismatales, Sordariales, Venturiales, Xylariales (Pezizomycotina) and Pneumocystidales, Schizosaccharomycetales and Taphrinales (Taphrinomycotina) are provided. Each diagram is explained with a representative genus/genera of their sexual and asexual cycles of each order. Within Pezizomycotina, Dothideomycetes contains the highest number of orders, with 57, followed by Sordariomycetes (52 orders), Lecanoromycetes (21 orders), Eurotiomycetes and Leotiomycetes (12 orders each), Laboulbeniomycetes (3 orders), and Arthoniomycetes and Xylonomycetes (2 orders each). Candelariomycetes, Coniocybomycetes, Geoglossomycetes, Lichinomycetes, Orbiliomycetes, Pezizomycetes, Sareomycetes, and Xylobotryomycetes each contain a single order, while Thelocarpales and Vezdaeales are treated as incertae sedis within Pezizomycotina. Notably, the classes Candelariomycetes, Coniocybomycetes, Geoglossomycetes, Sareomycetes, and Xylonomycetes, all recently grouped under Lichinomycetes, are treated as separate classes based on phylogenetic analysis and current literature. Within Lecanoromycetes, the synonymization of Sporastatiales with Rhizocarpales and Sarrameanales with Schaereriales is not supported in the phylogenetic analysis. These orders are retained separately, and the justifications are provided under each section as well as in the discussion. Within Leotiomycetes, the order Medeolariales, which was once considered part of Helotiales, is treated as a distinct order based on phylogenetic evidence. The classification of Medeolariales may change as more data becomes available from different gene regions. Lahmiales (Leotiomycetes) is not included in the phylogenetic analysis due to a lack of molecular data. Sareomycetes and Xylonomycetes are treated as separate classes. Spathulospora mixed with Lulworthiales and the inclusion of Spathulosporales within Lulworthiomycetidae is supported and extant molecular sampling is important to resolve the phylogenetic boundaries of members of this subclass. The majority of the classes of Pezizomycotina and Taphrinomycotina formed monophyletic clades in the phylogenetic analysis conducted based on SSU, LSU, 5.8S, TEF and RPB2 sequence data. However, Arthoniomycetes nested with the basal lineage of Dothideomycetes and formed a monophyletic clade also known as the superclass, Dothideomyceta. In Taphrinomycotina, a single order is accepted within each class.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 536-1411 |
| Number of pages | 876 |
| Journal | Mycosphere |
| Volume | 16 |
| Issue number | 1 |
| DOIs | |
| State | Published - 2025 |
Keywords
- Classification
- Morphology
- Pezizomycotina
- Phylogeny
- Taphrinomycotina
- taxonomy
ASJC Scopus subject areas
- Ecology, Evolution, Behavior and Systematics
- Plant Science
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In: Mycosphere, Vol. 16, No. 1, 2025, p. 536-1411.
Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Orders of Ascomycota
AU - Thiyagaraja, V.
AU - Hyde, K. D.
AU - Piepenbring, M.
AU - Davydov, E. A.
AU - Dai, D. Q.
AU - Abdollahzadeh, J.
AU - Bundhun, D.
AU - Chethana, K. W.T.
AU - Crous, P. W.
AU - Gajanayake, A. J.
AU - Gomdola, D.
AU - Haelewaters, D.
AU - Johnston, P. R.
AU - Mardones, M.
AU - Perera, R. H.
AU - Senanayake, I. C.
AU - Tibpromma, S.
AU - Yasanthika, W. A.E.
AU - Abbasi, M. W.
AU - Abdel-Wahab, M. A.
AU - Absalan, S.
AU - Acharya, K.
AU - Afshari, N.
AU - Aouali, S.
AU - Aptroot, A.
AU - Apurillo, C. C.S.
AU - Armand, A.
AU - Avasthi, S.
AU - Bao, D. F.
AU - Bhat, D. J.
AU - Blondelle, A.
AU - Boonmee, S.
AU - Boonyuen, N.
AU - Braun, U.
AU - Cadež, N.
AU - Calabon, M. S.
AU - Cazabonne, J.
AU - Chakraborty, N.
AU - Cheewangkoon, R.
AU - Chen, K. H.
AU - Coleine, C.
AU - Darmostuk, V.
AU - Daroodi, Z.
AU - Dasgupta, D.
AU - de Groot, M. D.
AU - De Hoog, S.
AU - Deng, W.
AU - Dissanayake, A. J.
AU - Dissanayake, L. S.
AU - Doilom, M.
AU - Dong, W.
AU - Dong, W.
AU - Ertz, D.
AU - Fortuna, J. L.
AU - Gautam, A. K.
AU - Gorczak, M.
AU - Groenewald, M.
AU - Groenewald, J. Z.
AU - Gunarathne, A.
AU - Han, Y.
AU - Hongsanan, S.
AU - Hou, C. L.
AU - Htet, Y. M.
AU - Htet, Z. H.
AU - Huang, Q.
AU - Huang, S. K.
AU - Huanraluek, N.
AU - Jayalal, R. G.U.
AU - Jayasiri, S. C.
AU - Jayawardena, R. S.
AU - Jiang, S. H.
AU - Jones, E. B.G.
AU - Karimi, O.
AU - Karunarathna, S. C.
AU - Khuna, S.
AU - Kossmann, T.
AU - Kularathnage, N. D.
AU - Lestari, A. S.
AU - Li, C. J.Y.
AU - Li, J. F.
AU - Lin, C. G.
AU - Liu, J. K.
AU - Liu, X.
AU - Liu, Y.
AU - Lu, L.
AU - Lu, Y. Z.
AU - Luo, Z. L.
AU - Ma, J.
AU - Madagammana, A. S.
AU - Maharachchikumbura, S. S.N.
AU - Marasinghe, D. S.
AU - Martzoukou, E.
AU - Marin-Felix, Y.
AU - Miller, A. N.
AU - Monkai, J.
AU - Noorabadi, M. T.
AU - Norphanphoun, C.
AU - Olariaga, I.
AU - Opiña, L. A.D.
AU - Pang, K. L.
AU - Peng, X.
AU - Péter, G.
AU - Phillips, A. J.L.
AU - Pineda, M. M.
AU - Prieto, M.
AU - Quan, Y.
AU - Quandt, A.
AU - Rajeshkumar, K. C.
AU - Rambold, G.
AU - Raymundo, T.
AU - Raza, M.
AU - Réblová, M.
AU - Samaradiwakara, N. P.
AU - Sarma, V. V.
AU - Schultz, M.
AU - Seifollahi, E.
AU - Selbmann, L.
AU - Su, H.
AU - Sun, Y. R.
AU - Tehler, A.
AU - Tennakoon, D. S.
AU - Thambugala, K. M.
AU - Tian, W. H.
AU - Tsurykau, A.
AU - Valenzuela, R.
AU - Verma, R. K.
AU - Wang, J.
AU - Wang, W. P.
AU - Wang, X. Y.
AU - Wang, Y.
AU - Wang, Z.
AU - Wei, D. P.
AU - Wen, T.
AU - Wijayawardene, N. N.
AU - Wimalasena, M. K.
AU - Worthy, F. R.
AU - Wu, H. X.
AU - Xu, L.
AU - Yakovchenko, L. S.
AU - Yu, F. M.
AU - Zeng, X. Y.
AU - Zhang, S. N.
AU - Zhang, Z. Y.
AU - Zhao, Q.
AU - Wanasinghe, D. N.
N1 - Vinodhini Thiyagaraja and Kevin D. Hyde thank the Chinese Research Fund (project no E1644111K1) entitled “Flexible introduction of high-level expert program, Kunming Institute of Botany, Chinese Academy of Sciences and The National Research Council of Thailand (NRCT) grant entitled “Total fungal diversity in a given forest area with implications towards species numbers, chemical diversity and biotechnology” (Grant no. N42A650547). Vinodhini Thiyagaraja also thanks National postdoctoral special funding, Yunnan Province "Caiyun Postdoctoral Program" in 2023, Choi Wan Postdoctoral Program 2023 and expresses gratitude to Prof. Robert Lücking for his guidance and support throughout the academic journey. Alan JL Phillips acknowledges the support from UID/00100, BioISI (DOI: 10.54499/UIDB/04046/2020) Centre grant from FCT, Portugal (to BioISI). André Aptroot thanks Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 001, who provided a visiting professorship to the author. Ashani D. Madagammana would like to thank Mae Fah Luang University (MFU) for the scholarship opportunity and Dr. Ausana Mapook for generously sharing the photographs of the members of Myucopronales with us. Tania Raymundo thanks to financial support received from CONAHCYT and IPN of Projects SIP-20230017 and 20230642. Mingkwan Doilom thanks Guangdong University Key Laboratory for Sustainable Control of Fruit and Vegetable Diseases and Pests (KA21031C502), and the Science and Technology Bureau of Guangzhou City (2023A04J1426) for funding this research. Claudia Coleine thanks the European Commission under the Marie Sklodowska-Curie Grant Agreement No. 702057 (DRYLIFE). C.C. and L.S. wish to thank the Italian National Program for Antarctic Research for funding sampling campaigns and research activities in Italy in the frame of PNRA projects. Cuijinyi Li thanks Second Tibetan Plateau Scientific Expedition and Research (STEP) Program (Grant No. 2019QZKK0503); The Survey of Wildlife Resources in Key Areas of Tibet (ZL202203601); Major science and technology projects and key R&D plans/programs, Yunnan Province (202202AE090001) for funding this research. Dhanushka Wanasinghe acknowledges the financial support provided under the Distinguished Scientist Fellowship Programme (DSFP), at King Saud University, Riyadh, Saudi Arabia. Dong-Qin Dai thanks High-Level Talent Recruitment Plan of Yunnan Provinces (“Young Talents” Program and “High-End Foreign Experts” Program). MS Calabon is grateful to the UP System Balik PhD Program (OVPAA-BPhD-2022-02) entitled, “Unraveling the hidden diversity of aquatic fungi from Panay Island, Philippines”. E. Seifollahi thanks, Dr. H. Raja and Prof. PW Crous, for giving us permission to use microscopy photographs. Evgeny A. Davydov grateful to Dr W. Obermayer (GZU), Dr A.V. Melekhin (KPABG), and Dr L. S. Yakovchenko (VLA) for providing photos. Feng-Ming Yu & Qi Zhao thanks Second Qinghai Tibet Plateau Scientific Investigation and Research Program (STEP). Program (Grant No. 2019QZKK0503), and the “Cross-Collaboration Group” Open Research Project of the Wild Species Germplasm Resource Bank, Kunming Institute of Botany, Chinese Academy of Sciences (Grant No. 292019312511043). Junfu Li thanks grants from Yunnan Department of Sciences and Technology of China (“Project on Key Technology for Ecological Restoration and Green Development in Tropical Dry-Hot Valley Grant No: 202302AE090023) for funding this research. Jutamart Monkai thankful for the partial support of Chiang Mai University, Thailand. K. W. Thilini Chethana and Omid Karimi thanks the Basic Research Fund (Fundamental Fund) of the National Science, Research and Innovation Fund (Grant No. 662A01003, 672A01003) entitled ‘Taxonomy, Phylogeny and chemo-profiling of selected families in Xylariales’ for funding the research. Sinang Hongsanan thanks the grants provided by the College of Life Science and Oceanography at Shenzhen University and Dr. Dong Qin Dai, Dr. Saranyaphat Boonmee and Dr. Wu HaiXia to contribute their fungal pictures. Li Lu thanks Mae Fah Luang University for the award of a fee-less scholarship and the Center for Yunnan Plateau Biological Resources Protection and Utilization, College of Biological Resource and Food Engineering, Qujing Normal University is thanked for the facilities provided for the research work. Lijian Xu thanks the National Natural Science Foundation of China (no. 31870528) and the Natural Science Foundation of Heilongjiang Province (LH2023C092). Samantha C. Karunarathna thanks the National Natural Science Foundation of China (No. 32260004) and Yunnan Revitalization Talents Support Plan (High-End Foreign Experts Program) for their support. Lidia S. Yakovchenko grateful to Evgeny A. Davydov, Bruce McCune, Jan Vondrák, J. A. Elix for providing specimens for taxa of Candelariales as well as Irina Urbanavichene for sending specimens of Pycnora from LE. I appreciate Jason Hollinger’s provision of photos for Placomaronea. The research of LY was carried out within the state assignment of Ministry of Science and Higher Education of the Russian Federation (theme No. 121031000117-9). Martina Réblová thanks to a long-term research development project of the Czech Academy of Sciences, Institute of Botany (RVO 67985939). Kunhiraman C. Rajeshkumar would like to thank the Science and Engineering Research Board (SERB), the Department of Science and Technology, Government of India, for their financial support through the CRG/2020/000668 project and also thank Dr. P. K. Dhakephalkar, Director of the MACS Agharkar Research Institute in Pune, for motivating us in our research work. Mingkwan Doilom thanks the foundation of Guangzhou Bureau of Science and Technology (grant no. 2023A04J1426), the Guangdong Provincial College Key Laboratory of Green Prevention and Control of Fruit and Vegetable Pests and Diseases (grant no. KA21031C502) and the Talent Program of Zhongkai University of Agricultural and Engineering (grant no. KA22016B746). Nattawut Boonyuen thanks National Center for Genetic Engineering and Biotechnology and National Science and Technology Development Agency (project numbers: P2450748, P2451951 and P2451576). CCS Apurillo would like to thank the Mae Fah Luang University for the partial PhD scholarship grant (GR-ST-PS-65-21) and the Department of Science and Technology-Philippine Science High School Eastern Visayas Campus for the study leave grant. Omid Karimi would like to thank the Mae Fah Luang University Partial Scholarship for the doctoral degree program and Mushroom Research Foundation. Omid Karimi thanks Prof. Dinushani A. Daranagama, Dr. Milan C. Samarakoon, and Dr. Siranapa Konta for sharing some photos with us. Raza M is grateful for support and project funding from ‘Agriculture Sci-tech Renovation’ (XJNKYWDZC–2022004). Peter Jhonston thanks to Konstanze Bensch, Mycobank, for providing the epitype data. Johnston was supported through the Manaaki Whenua Biota Portfolio with funding from the Strategic Science Investment Fund of the New Zealand Ministry of Business, Innovation and Employment. Melissa Mardones thanks to grants (ALE-COSTA) from the University of Costa Rica (OAICE) and DAAD for funding this research and Vicerrectoría de Investigación (UCR), project number 111-B8-284, for partially funding this work. Thiago Kossmann & C. Alisha Quandt grateful for funding from the US National Science Foundation DEB-2018215 to CAQ. TK thanks CAPES/Fulbright (Edital 05/2021). Xiang-Yu Zeng thanks Natural Science Special Research Fund of Guizhou University, Special Post 2021(25); China Scholarship Council [2021]15 no. 202108520071. Andreas Beck (M) is thanked for providing the habitus photographs. Yanfeng Han grateful to grants from the “Hundred” Talent Projects of Guizhou Province (Qian Ke He [2020] 6005) and the Natural Science Foundation of China (No. 32060011, 32160007) for funding this research. Zhang Shengnan thanks to Yang J, Yu XD and Du HZ for their contributions of the photos that used as representatives for each genus. Yasmina Marin-Felix is grateful to the Deutsche Forschungsgemeinschaft (DFG) for the support of COPFUN Project (ID 490821847). Zhi-Yuan Zhang thanks Guizhou Provincial Science and Technology Projects (ZK[2023]155). Evgeny A. Davydov thanks National Natural Science Foundation of China (No. 31870629 and 32270012) and the German Federal Ministry of Education and Research (BMBF, 01DG20015FunTrAf). Wei Dong thanks the National Natural Science Foundation of China (grant No. 32200015), and the Foundation of Guangzhou Bureau of Science and Technology (grant No. 2023A04J1425). E.B.G. Jones is supported under the Distinguished Scientist Fellowship Program (DSFP), King Saud University, Kingdom of Saudi Arabia. D. Jayarama Bhat gratefully acknowledges the financial support provided under the Distinguished Scientist Fellowship Programme (DSFP), at King Saud University, Riyadh, Saudi Arabia. Chada Norphanphoun thanks the China Postdoctoral Science Foundation Assistance Act. and Postdoctoral Management Regulations of Guizhou University (No. [2019] 65). N. Čadež gratefully acknowledges financial support from the Slovenian Research and Innovation Agency, grants P4–0116 and MRIC-UL ZIM, IP-0510. Naghmeh Afshari and Nethmini P. Samaradiwakara would like to thank Chiang Mai University for providing the Presidential Scholarship 2020 and Mae Fah Luang University for the research collaboration. V.V. Sarma would like to thank the Ministry of Earth Sciences (MOES), Govt. of India for funding a project (MOES/36/OOIS/Extra/77/2020 dt.26.07.2021) and the Science and Engineering Research Board (SERB), Govt. of India for a financial support (CRG/2021/005223C dt.15.12.2021) and HOD, Department of Biotechnology, Pondicherry University for facilities. Xiang-Yu Zeng thanks Guizhou Provincial Basic Research Program (Natural Science) ZK[2023] general 087. Zin Hnin Htet thanks Basic Research Fund support from the National Science, Research and Innovation Fund (Grant No. 652A01001). Fiona Ruth Worthy acknowledges the Yunnan Provincial Science and Technology Department Intelligent Yunnan Young Scientist grant (02303AM140006). V. Darmostuk received additional support under statutory funds from the W. Szafer Institute of Botany, Polish Academy of Sciences. Carlo Chris S. Apurillo thanks the Mae Fah Luang University for partial scholarship grant (GR-ST-PS-65-21); Mushroom Research Foundation and the Department of Science and Technology-Philippine Science High School-Eastern Visayas Campus for grant of study leave. Samantha C. Karunarathna and Saowaluck Tibpromma thank the National Natural Science Foundation of China (No. 32260004), Yunnan Revitalization Talents Support Plan (High-End Foreign Experts Program) and the Key Laboratory of Yunnan Provincial Department of Education of the Deep-Time Evolution on Biodiversity from the Origin of the Pearl River for their support. Danfeng Bao would like to thank the Postdoctoral Fellowship Program of CPSF under Grant Number GZC20240346. Shi-Ke Huang acknowledges the China Postdoctoral Science Foundation (No: 2023MD744196) and the Department of Education of Guizhou Province (No: [2022] 310). Vinodhini Thiyagaraja also thank Gao Ying, ZhiXiu Qian and Achala Rathnayaka for providing the pictures for entries. Shu-Hua Jiang thanks the National Natural Science Foundation of China (Grant No. 32270007, 31750001), and the Chinese Academy of Sciences (Program CAS TAX-24-022) for financial support. Wu Hai-Xia is grateful to grants from the National Natural Science Foundation of China (grant No. 32170024), the Yunnan Province Ten Thousand Plan of Youth Top Talent Project (No. YNWR-QNBJ-2018-267) and the Yunnan Fundamental Research Projects (grant No. 202401AT070017). Tingchi Wen and his team thank National Natural Science Foundation of China (No. 32060012).
PY - 2025
Y1 - 2025
N2 - Ascomycota, the most speciose phylum of fungi, is a complex entity, comprising three diverse subphyla: Pezizomycotina, Saccharomycotina, and Taphrinomycotina. The largest and most diverse subphylum, Pezizomycotina, is a rich tapestry of 16 classes and 171 orders. Saccharomycotina, the second largest subphylum, is a diverse collection of seven classes and 12 orders, while Taphrinomycotina, the smallest, is a unique assembly of six classes and six orders. Over the past decade, numerous taxonomic studies have focused on the generic, family, and class classifications of Ascomycota. These efforts, well-documented across various databases, are crucial for a comprehensive understanding of the classification. However, the study of taxonomy at the ordinal level, a crucial tier in the taxonomic hierarchy, has been largely overlooked. In a global collaboration with mycologists and lichenologists, this study presents the first comprehensive information on the orders within Pezizomycotina and Taphrinomycotina. The recent taxonomic classification of Saccharomycotina has led to the exclusion of this subphylum from the present study, as an immediate revision is not necessary. Each order is thoroughly discussed, highlighting its historical significance, current status, key identification characteristics, evolutionary relationships, ecological and economic roles, future recommendations, and updated family-level classification. Teaching diagrams for the life cycles of several orders, viz. Asterinales, Helotiales, Hypocreales, Laboulbeniales, Meliolales, Mycosphaerellales, Ophiostomatales, Pezizales, Pleosporales, Phyllachorales, Rhytismatales, Sordariales, Venturiales, Xylariales (Pezizomycotina) and Pneumocystidales, Schizosaccharomycetales and Taphrinales (Taphrinomycotina) are provided. Each diagram is explained with a representative genus/genera of their sexual and asexual cycles of each order. Within Pezizomycotina, Dothideomycetes contains the highest number of orders, with 57, followed by Sordariomycetes (52 orders), Lecanoromycetes (21 orders), Eurotiomycetes and Leotiomycetes (12 orders each), Laboulbeniomycetes (3 orders), and Arthoniomycetes and Xylonomycetes (2 orders each). Candelariomycetes, Coniocybomycetes, Geoglossomycetes, Lichinomycetes, Orbiliomycetes, Pezizomycetes, Sareomycetes, and Xylobotryomycetes each contain a single order, while Thelocarpales and Vezdaeales are treated as incertae sedis within Pezizomycotina. Notably, the classes Candelariomycetes, Coniocybomycetes, Geoglossomycetes, Sareomycetes, and Xylonomycetes, all recently grouped under Lichinomycetes, are treated as separate classes based on phylogenetic analysis and current literature. Within Lecanoromycetes, the synonymization of Sporastatiales with Rhizocarpales and Sarrameanales with Schaereriales is not supported in the phylogenetic analysis. These orders are retained separately, and the justifications are provided under each section as well as in the discussion. Within Leotiomycetes, the order Medeolariales, which was once considered part of Helotiales, is treated as a distinct order based on phylogenetic evidence. The classification of Medeolariales may change as more data becomes available from different gene regions. Lahmiales (Leotiomycetes) is not included in the phylogenetic analysis due to a lack of molecular data. Sareomycetes and Xylonomycetes are treated as separate classes. Spathulospora mixed with Lulworthiales and the inclusion of Spathulosporales within Lulworthiomycetidae is supported and extant molecular sampling is important to resolve the phylogenetic boundaries of members of this subclass. The majority of the classes of Pezizomycotina and Taphrinomycotina formed monophyletic clades in the phylogenetic analysis conducted based on SSU, LSU, 5.8S, TEF and RPB2 sequence data. However, Arthoniomycetes nested with the basal lineage of Dothideomycetes and formed a monophyletic clade also known as the superclass, Dothideomyceta. In Taphrinomycotina, a single order is accepted within each class.
AB - Ascomycota, the most speciose phylum of fungi, is a complex entity, comprising three diverse subphyla: Pezizomycotina, Saccharomycotina, and Taphrinomycotina. The largest and most diverse subphylum, Pezizomycotina, is a rich tapestry of 16 classes and 171 orders. Saccharomycotina, the second largest subphylum, is a diverse collection of seven classes and 12 orders, while Taphrinomycotina, the smallest, is a unique assembly of six classes and six orders. Over the past decade, numerous taxonomic studies have focused on the generic, family, and class classifications of Ascomycota. These efforts, well-documented across various databases, are crucial for a comprehensive understanding of the classification. However, the study of taxonomy at the ordinal level, a crucial tier in the taxonomic hierarchy, has been largely overlooked. In a global collaboration with mycologists and lichenologists, this study presents the first comprehensive information on the orders within Pezizomycotina and Taphrinomycotina. The recent taxonomic classification of Saccharomycotina has led to the exclusion of this subphylum from the present study, as an immediate revision is not necessary. Each order is thoroughly discussed, highlighting its historical significance, current status, key identification characteristics, evolutionary relationships, ecological and economic roles, future recommendations, and updated family-level classification. Teaching diagrams for the life cycles of several orders, viz. Asterinales, Helotiales, Hypocreales, Laboulbeniales, Meliolales, Mycosphaerellales, Ophiostomatales, Pezizales, Pleosporales, Phyllachorales, Rhytismatales, Sordariales, Venturiales, Xylariales (Pezizomycotina) and Pneumocystidales, Schizosaccharomycetales and Taphrinales (Taphrinomycotina) are provided. Each diagram is explained with a representative genus/genera of their sexual and asexual cycles of each order. Within Pezizomycotina, Dothideomycetes contains the highest number of orders, with 57, followed by Sordariomycetes (52 orders), Lecanoromycetes (21 orders), Eurotiomycetes and Leotiomycetes (12 orders each), Laboulbeniomycetes (3 orders), and Arthoniomycetes and Xylonomycetes (2 orders each). Candelariomycetes, Coniocybomycetes, Geoglossomycetes, Lichinomycetes, Orbiliomycetes, Pezizomycetes, Sareomycetes, and Xylobotryomycetes each contain a single order, while Thelocarpales and Vezdaeales are treated as incertae sedis within Pezizomycotina. Notably, the classes Candelariomycetes, Coniocybomycetes, Geoglossomycetes, Sareomycetes, and Xylonomycetes, all recently grouped under Lichinomycetes, are treated as separate classes based on phylogenetic analysis and current literature. Within Lecanoromycetes, the synonymization of Sporastatiales with Rhizocarpales and Sarrameanales with Schaereriales is not supported in the phylogenetic analysis. These orders are retained separately, and the justifications are provided under each section as well as in the discussion. Within Leotiomycetes, the order Medeolariales, which was once considered part of Helotiales, is treated as a distinct order based on phylogenetic evidence. The classification of Medeolariales may change as more data becomes available from different gene regions. Lahmiales (Leotiomycetes) is not included in the phylogenetic analysis due to a lack of molecular data. Sareomycetes and Xylonomycetes are treated as separate classes. Spathulospora mixed with Lulworthiales and the inclusion of Spathulosporales within Lulworthiomycetidae is supported and extant molecular sampling is important to resolve the phylogenetic boundaries of members of this subclass. The majority of the classes of Pezizomycotina and Taphrinomycotina formed monophyletic clades in the phylogenetic analysis conducted based on SSU, LSU, 5.8S, TEF and RPB2 sequence data. However, Arthoniomycetes nested with the basal lineage of Dothideomycetes and formed a monophyletic clade also known as the superclass, Dothideomyceta. In Taphrinomycotina, a single order is accepted within each class.
KW - Classification
KW - Morphology
KW - Pezizomycotina
KW - Phylogeny
KW - Taphrinomycotina
KW - taxonomy
UR - https://www.scopus.com/pages/publications/105008231799
UR - https://www.scopus.com/pages/publications/105008231799#tab=citedBy
U2 - 10.5943/mycosphere/16/1/8
DO - 10.5943/mycosphere/16/1/8
M3 - Article
AN - SCOPUS:105008231799
SN - 2077-7000
VL - 16
SP - 536
EP - 1411
JO - Mycosphere
JF - Mycosphere
IS - 1
ER -