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1. The numbers of fungi: are the most speciose genera truly diverse?

Author

Bhunjun, Chitrabhanu S., primary, Niskanen, Tuula, additional, Suwannarach, Nakarin, additional, Wannathes, Nopparat, additional, Chen, Yi-Jyun, additional, McKenzie, Eric H. C., additional, Maharachchikumbura, Sajeewa S. N., additional, Buyck, Bart, additional, Zhao, Chang-Lin, additional, Fan, Yu-Guang, additional, Zhang, Jing-Yi, additional, Dissanayake, Asha J., additional, Marasinghe, Diana S., additional, Jayawardena, Ruvishika S., additional, Kumla, Jaturong, additional, Padamsee, Mahajabeen, additional, Chen, Ya-Ya, additional, Liimatainen, Kare, additional, Ammirati, Joseph F., additional, Phukhamsakda, Chayanard, additional, Liu, Jian-Kui, additional, Phonrob, Wiphawanee, additional, Randrianjohany, Émile, additional, Hongsanan, Sinang, additional, Cheewangkoon, Ratchadawan, additional, Bundhun, Digvijayini, additional, Khuna, Surapong, additional, Yu, Wen-Jie, additional, Deng, Lun-Sha, additional, Lu, Yong-Zhong, additional, Hyde, Kevin D., additional, and Lumyong, Saisamorn, additional

Published
2022
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2. Species diversity of Basidiomycota

Author

He, Mao-Qiang, primary, Zhao, Rui-Lin, additional, Liu, Dong-Mei, additional, Denchev, Teodor T., additional, Begerow, Dominik, additional, Yurkov, Andrey, additional, Kemler, Martin, additional, Millanes, Ana M., additional, Wedin, Mats, additional, McTaggart, A. R., additional, Shivas, Roger G., additional, Buyck, Bart, additional, Chen, Jie, additional, Vizzini, Alfredo, additional, Papp, Viktor, additional, Zmitrovich, Ivan V., additional, Davoodian, Naveed, additional, and Hyde, Kevin D., additional

Published
2022
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3. Fungal diversity notes 1036–1150: taxonomic and phylogenetic contributions on genera and species of fungal taxa

Author

Anuruddha Karunarathna, Touny Sorvongxay, Jacques Fournier, Martina Réblová, Sally C. Fryar, Yuan-Pin Xiao, Erio Camporesi, Rashika S. Brahmanage, Saranyaphat Boonmee, Thuong T. T. Nguyen, Chayanard Phukhamsakda, Sinang Hongsanan, William Kalhy Silva Xavier, Janith V. S. Aluthmuhandiram, Sun Jeong Jeon, Jing Yang, Yong Zhong Lu, Jos Houbraken, Hong-Bo Jiang, Jadson D. P. Bezerra, José Ewerton Felinto dos Santos, Anusha H. Ekanayaka, Yusufjon Gafforov, Napalai Chaiwan, D. Jayarama Bhat, V.P. Abreu, Jie Chen, Sheng-Nan Zhang, Helio Longoni Plautz, Nimali I. de Silva, Kevin D. Hyde, De-Ping Wei, Guangshuo Li, Rajesh Jeewon, Vinodhini Thiyagaraja, Jianchu Xu, Jens Christian Frisvad, André Aptroot, Rekhani H. Perera, Rui-Lin Zhao, Hyang Burm Lee, Kunthida Phutthacharoen, Neiva Tinti de Oliveira, Jian-Kui Liu, Milan C. Samarakoon, Robert Lücking, Thilini Chethana, Paul M. Kirk, Zong-Long Luo, Ruvishika S. Jayawardena, Peter E. Mortimer, Junmin Liang, Subashini C. Jayasiri, Dulanjalee Harishchandra, Digvijayini Bundhun, Buyck Bart, Renan do Nascimento Barbosa, Chada Norphanphoun, Damien Ertz, Monika C. Dayarathne, Samantha C. Karunarathna, Paras Nath Singh, Itthayakorn Promputtha, Sajeewa S. N. Maharachchikumbura, André Wilson Campos Rosado, Vinit Kumar, Jana Nekvindová, Eleni Gentekaki, Marcela Eugenia da Silva Cáceres, Yu Cheng Dai, Qiu Ju Shang, Hye Yeon Mun, Wei Dong, Xiang Yu Zeng, Armin Mešić, Indunil C. Senanayake, Chuan Gen Lin, Tuula Niskanen, E. B. Gareth Jones, Kare Liimatainen, Dan Feng Bao, Sirinapa Konta, Thays Gabrielle Lins de Oliveira, Olinto Liparini Pereira, Jin-Feng Zhang, Kasun M. Thambugala, Xiao Hong Ji, Timur S. Bulgakov, Pranami D. Abeywickrama, Ishara S. Manawasinghe, Oliane Maria Correia Magalhães, Qi Zhao, Walter Rossi, Cristina Maria de Souza-Motta, Xue Mei Tian, Valérie Hofstetter, Putarak Chomnunti, Guo Jie Li, Sanjay K. Singh, Ming Zeng, Adriene Mayra Soares, Dhandevi Pem, Ishani D. Goonasekara, Helen Maria Pontes Sotão, Frank Bungartz, Mingkwan Doilom, Rungtiwa Phookamsak, Ji Ye Yan, Emile Randrianjohany, Zdenko Tkalčec, Marco Leonardi, Chang Hsin Kuo, Dhanushka N. Wanasinghe, Ting-Chi Wen, Shi Ke Huang, Erandi Yasanthika, Danushka S. Tennakoon, Saisamorn Lumyong, Alan J. L. Phillips, Tatiana Baptista Gibertoni, Lei Cai, Westerdijk Fungal Biodiversity Institute - Food and Indoor Mycology, and Westerdijk Fungal Biodiversity Institute

Subjects
Leotiomycetes, Ascomycota, 71 new taxa, Basidiomycota, Dothideomycetes, Eurotiomycetes, Lecanoromycetes, Pezizomycetes, Phylogeny, Taxonomy, s<%2Fbold>%22">Dothideomycetes, Botany, Ecology, Evolution, Behavior and Systematics, Cantharellus, Fomitiporia, Ecology, biology, Coprinopsis, biology.organism_classification, Russula, Cortinarius, Dothiorella, Buellia
Abstract

This article is the tenth series of the Fungal Diversity Notes, where 114 taxa distributed in three phyla, ten classes, 30 orders and 53 families are described and illustrated. Taxa described in the present study include one new family (viz. Pseudoberkleasmiaceae in Dothideomycetes), five new genera (Caatingomyces, Cryptoschizotrema, Neoacladium, Paramassaria and Trochilispora) and 71 new species, (viz. Acrogenospora thailandica, Amniculicola aquatica, A. guttulata, Angustimassarina sylvatica, Blackwellomyces lateris, Boubovia gelatinosa, Buellia viridula, Caatingomyces brasiliensis, Calophoma humuli, Camarosporidiella mori, Canalisporium dehongense, Cantharellus brunneopallidus, C. griseotinctus, Castanediella meliponae, Coprinopsis psammophila, Cordyceps succavus, Cortinarius minusculus, C. subscotoides, Diaporthe italiana, D. rumicicola, Diatrypella delonicis, Dictyocheirospora aquadulcis, D. taiwanense, Digitodesmium chiangmaiense, Distoseptispora dehongensis, D. palmarum, Dothiorella styphnolobii, Ellisembia aurea, Falciformispora aquatic, Fomitiporia carpinea, F. lagerstroemiae, Grammothele aurantiaca, G. micropora, Hermatomyces bauhiniae, Jahnula queenslandica, Kamalomyces mangrovei, Lecidella yunnanensis, Micarea squamulosa, Muriphaeosphaeria angustifoliae, Neoacladium indicum, Neodidymelliopsis sambuci, Neosetophoma miscanthi, N. salicis, Nodulosphaeria aquilegiae, N. thalictri, Paramassaria samaneae, Penicillium circulare, P. geumsanense, P. mali-pumilae, P. psychrotrophicum, P. wandoense, Phaeoisaria siamensis, Phaeopoacea asparagicola, Phaeosphaeria penniseti, Plectocarpon galapagoense, Porina sorediata, Pseudoberkleasmium chiangmaiense, Pyrenochaetopsis sinensis, Rhizophydium koreanum, Russula prasina, Sporoschisma chiangraiense, Stigmatomyces chamaemyiae, S. cocksii, S. papei, S. tschirnhausii, S. vikhrevii, Thysanorea uniseptata, Torula breviconidiophora, T. polyseptata, Trochilispora schefflerae and Vaginatispora palmae). Further, twelve new combinations (viz. Cryptoschizotrema cryptotrema, Prolixandromyces australi, P. elongatus, P. falcatus, P. longispinae, P. microveliae, P. neoalardi, P. polhemorum, P. protuberans, P. pseudoveliae, P. tenuistipitis and P. umbonatus), an epitype is chosen for Cantharellus goossensiae, a reference specimen for Acrogenospora sphaerocephala and new synonym Prolixandromyces are designated. Twenty-four new records on new hosts and new geographical distributions are also reported (i.e. Acrostalagmus annulatus, Cantharellus goossensiae, Coprinopsis villosa, Dothiorella plurivora, Dothiorella rhamni, Dothiorella symphoricarposicola, Dictyocheirospora rotunda, Fasciatispora arengae, Grammothele brasiliensis, Lasiodiplodia iraniensis, Lembosia xyliae, Morenoina palmicola, Murispora cicognanii, Neodidymelliopsis farokhinejadii, Neolinocarpon rachidis, Nothophoma quercina, Peroneutypa scoparia, Pestalotiopsis aggestorum, Pilidium concavum, Plagiostoma salicellum, Protofenestella ulmi, Sarocladium kiliense, Tetraploa nagasakiensis and Vaginatispora armatispora).

Published
2019

4. Notes, outline and divergence times of Basidiomycota

Author

He, Mao-Qiang, primary, Zhao, Rui-Lin, additional, Hyde, Kevin D., additional, Begerow, Dominik, additional, Kemler, Martin, additional, Yurkov, Andrey, additional, McKenzie, Eric H. C., additional, Raspé, Olivier, additional, Kakishima, Makoto, additional, Sánchez-Ramírez, Santiago, additional, Vellinga, Else C., additional, Halling, Roy, additional, Papp, Viktor, additional, Zmitrovich, Ivan V., additional, Buyck, Bart, additional, Ertz, Damien, additional, Wijayawardene, Nalin N., additional, Cui, Bao-Kai, additional, Schoutteten, Nathan, additional, Liu, Xin-Zhan, additional, Li, Tai-Hui, additional, Yao, Yi-Jian, additional, Zhu, Xin-Yu, additional, Liu, An-Qi, additional, Li, Guo-Jie, additional, Zhang, Ming-Zhe, additional, Ling, Zhi-Lin, additional, Cao, Bin, additional, Antonín, Vladimír, additional, Boekhout, Teun, additional, da Silva, Bianca Denise Barbosa, additional, De Crop, Eske, additional, Decock, Cony, additional, Dima, Bálint, additional, Dutta, Arun Kumar, additional, Fell, Jack W., additional, Geml, József, additional, Ghobad-Nejhad, Masoomeh, additional, Giachini, Admir J., additional, Gibertoni, Tatiana B., additional, Gorjón, Sergio P., additional, Haelewaters, Danny, additional, He, Shuang-Hui, additional, Hodkinson, Brendan P., additional, Horak, Egon, additional, Hoshino, Tamotsu, additional, Justo, Alfredo, additional, Lim, Young Woon, additional, Menolli, Nelson, additional, Mešić, Armin, additional, Moncalvo, Jean-Marc, additional, Mueller, Gregory M., additional, Nagy, László G., additional, Nilsson, R. Henrik, additional, Noordeloos, Machiel, additional, Nuytinck, Jorinde, additional, Orihara, Takamichi, additional, Ratchadawan, Cheewangkoon, additional, Rajchenberg, Mario, additional, Silva-Filho, Alexandre G. S., additional, Sulzbacher, Marcelo Aloisio, additional, Tkalčec, Zdenko, additional, Valenzuela, Ricardo, additional, Verbeken, Annemieke, additional, Vizzini, Alfredo, additional, Wartchow, Felipe, additional, Wei, Tie-Zheng, additional, Weiß, Michael, additional, Zhao, Chang-Lin, additional, and Kirk, Paul M., additional

Published
2019
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5. The quest for a globally comprehensible Russula language

Author

Adamčík, Slavomír, primary, Looney, Brian, additional, Caboň, Miroslav, additional, Jančovičová, Soňa, additional, Adamčíková, Katarína, additional, Avis, Peter G., additional, Barajas, Magdalena, additional, Bhatt, Rajendra P., additional, Corrales, Adriana, additional, Das, Kanad, additional, Hampe, Felix, additional, Ghosh, Aniket, additional, Gates, Genevieve, additional, Kälviäinen, Ville, additional, Khalid, Abdul Nasir, additional, Kiran, Munazza, additional, De Lange, Ruben, additional, Lee, Hyun, additional, Lim, Young Woon, additional, Kong, Alejandro, additional, Manz, Cathrin, additional, Ovrebo, Clark, additional, Saba, Malka, additional, Taipale, Tero, additional, Verbeken, Annemieke, additional, Wisitrassameewong, Komsit, additional, and Buyck, Bart, additional

Published
2019
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8. Fungal diversity notes 603–708: taxonomic and phylogenetic notes on genera and species

Author

Hyde, Kevin D., primary, Norphanphoun, Chada, additional, Abreu, Vanessa P., additional, Bazzicalupo, Anna, additional, Thilini Chethana, K. W., additional, Clericuzio, Marco, additional, Dayarathne, Monika C., additional, Dissanayake, Asha J., additional, Ekanayaka, Anusha H., additional, He, Mao-Qiang, additional, Hongsanan, Sinang, additional, Huang, Shi-Ke, additional, Jayasiri, Subashini C., additional, Jayawardena, Ruvishika S., additional, Karunarathna, Anuruddha, additional, Konta, Sirinapa, additional, Kušan, Ivana, additional, Lee, Hyun, additional, Li, Junfu, additional, Lin, Chuan-Gen, additional, Liu, Ning-Guo, additional, Lu, Yong-Zhong, additional, Luo, Zong-Long, additional, Manawasinghe, Ishara S., additional, Mapook, Ausana, additional, Perera, Rekhani H., additional, Phookamsak, Rungtiwa, additional, Phukhamsakda, Chayanard, additional, Siedlecki, Igor, additional, Soares, Adriene Mayra, additional, Tennakoon, Danushka S., additional, Tian, Qing, additional, Tibpromma, Saowaluck, additional, Wanasinghe, Dhanushka N., additional, Xiao, Yuan-Pin, additional, Yang, Jing, additional, Zeng, Xiang-Yu, additional, Abdel-Aziz, Faten A., additional, Li, Wen-Jing, additional, Senanayake, Indunil C., additional, Shang, Qiu-Ju, additional, Daranagama, Dinushani A., additional, de Silva, Nimali I., additional, Thambugala, Kasun M., additional, Abdel-Wahab, Mohamed A., additional, Bahkali, Ali H., additional, Berbee, Mary L., additional, Boonmee, Saranyaphat, additional, Bhat, D. Jayarama, additional, Bulgakov, Timur S., additional, Buyck, Bart, additional, Camporesi, Erio, additional, Castañeda-Ruiz, Rafael F., additional, Chomnunti, Putarak, additional, Doilom, Minkwan, additional, Dovana, Francesco, additional, Gibertoni, Tatiana B., additional, Jadan, Margita, additional, Jeewon, Rajesh, additional, Jones, E. B. Gareth, additional, Kang, Ji-Chuan, additional, Karunarathna, Samantha C., additional, Lim, Young Woon, additional, Liu, Jian-Kui, additional, Liu, Zuo-Yi, additional, Plautz, Helio Longoni, additional, Lumyong, Saisamorn, additional, Maharachchikumbura, Sajeewa S. N., additional, Matočec, Neven, additional, McKenzie, Eric H. C., additional, Mešić, Armin, additional, Miller, Daniel, additional, Pawłowska, Julia, additional, Pereira, Olinto L., additional, Promputtha, Itthayakorn, additional, Romero, Andrea I., additional, Ryvarden, Leif, additional, Su, Hong-Yan, additional, Suetrong, Satinee, additional, Tkalčec, Zdenko, additional, Vizzini, Alfredo, additional, Wen, Ting-Chi, additional, Wisitrassameewong, Komsit, additional, Wrzosek, Marta, additional, Xu, Jian-Chu, additional, Zhao, Qi, additional, Zhao, Rui-Lin, additional, and Mortimer, Peter E., additional

Published
2017
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10. Fungal diversity notes 367–490: taxonomic and phylogenetic contributions to fungal taxa

Author

Hyde, Kevin D., primary, Hongsanan, Sinang, additional, Jeewon, Rajesh, additional, Bhat, D. Jayarama, additional, McKenzie, Eric H. C., additional, Jones, E. B. Gareth, additional, Phookamsak, Rungtiwa, additional, Ariyawansa, Hiran A., additional, Boonmee, Saranyaphat, additional, Zhao, Qi, additional, Abdel-Aziz, Faten Awad, additional, Abdel-Wahab, Mohamed A., additional, Banmai, Supharat, additional, Chomnunti, Putarak, additional, Cui, Bao-Kai, additional, Daranagama, Dinushani A., additional, Das, Kanad, additional, Dayarathne, Monika C., additional, de Silva, Nimali I., additional, Dissanayake, Asha J., additional, Doilom, Mingkwan, additional, Ekanayaka, Anusha H., additional, Gibertoni, Tatiana Baptista, additional, Góes-Neto, Aristóteles, additional, Huang, Shi-Ke, additional, Jayasiri, Subashini C., additional, Jayawardena, Ruvishika S., additional, Konta, Sirinapa, additional, Lee, Hyang Burm, additional, Li, Wen-Jing, additional, Lin, Chuan-Gen, additional, Liu, Jian-Kui, additional, Lu, Yong-Zhong, additional, Luo, Zong-Long, additional, Manawasinghe, Ishara S., additional, Manimohan, Patinjareveettil, additional, Mapook, Ausana, additional, Niskanen, Tuula, additional, Norphanphoun, Chada, additional, Papizadeh, Moslem, additional, Perera, Rekhani H., additional, Phukhamsakda, Chayanard, additional, Richter, Christian, additional, de A. Santiago, André L. C. M., additional, Drechsler-Santos, E. Ricardo, additional, Senanayake, Indunil C., additional, Tanaka, Kazuaki, additional, Tennakoon, T. M. D. S., additional, Thambugala, Kasun M., additional, Tian, Qing, additional, Tibpromma, Saowaluck, additional, Thongbai, Benjarong, additional, Vizzini, Alfredo, additional, Wanasinghe, Dhanushka N., additional, Wijayawardene, Nalin N., additional, Wu, Hai-Xia, additional, Yang, Jing, additional, Zeng, Xiang-Yu, additional, Zhang, Huang, additional, Zhang, Jin-Feng, additional, Bulgakov, Timur S., additional, Camporesi, Erio, additional, Bahkali, Ali H., additional, Amoozegar, Mohammad A., additional, Araujo-Neta, Lidia Silva, additional, Ammirati, Joseph F., additional, Baghela, Abhishek, additional, Bhatt, R. P., additional, Bojantchev, Dimitar, additional, Buyck, Bart, additional, da Silva, Gladstone Alves, additional, de Lima, Catarina Letícia Ferreira, additional, de Oliveira, Rafael José Vilela, additional, de Souza, Carlos Alberto Fragoso, additional, Dai, Yu-Cheng, additional, Dima, Bálint, additional, Duong, Tham Thi, additional, Ercole, Enrico, additional, Mafalda-Freire, Fernando, additional, Ghosh, Aniket, additional, Hashimoto, Akira, additional, Kamolhan, Sutakorn, additional, Kang, Ji-Chuan, additional, Karunarathna, Samantha C., additional, Kirk, Paul M., additional, Kytövuori, Ilkka, additional, Lantieri, Angela, additional, Liimatainen, Kare, additional, Liu, Zuo-Yi, additional, Liu, Xing-Zhong, additional, Lücking, Robert, additional, Medardi, Gianfranco, additional, Mortimer, Peter E., additional, Nguyen, Thi Thuong Thuong, additional, Promputtha, Itthayakorn, additional, Raj, K. N. Anil, additional, Reck, Mateus A., additional, Lumyong, Saisamorn, additional, Shahzadeh-Fazeli, Seyed Abolhassan, additional, Stadler, Marc, additional, Soudi, Mohammad Reza, additional, Su, Hong-Yan, additional, Takahashi, Takumasa, additional, Tangthirasunun, Narumon, additional, Uniyal, Priyanka, additional, Wang, Yong, additional, Wen, Ting-Chi, additional, Xu, Jian-Chu, additional, Zhang, Zhong-Kai, additional, Zhao, Yong-Chang, additional, Zhou, Jun-Liang, additional, and Zhu, Lin, additional

Published
2016
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11. Walking the thin line… ten years later: the dilemma of above- versus below-ground features to support phylogenies in the <italic>Russulaceae</italic> (Basidiomycota).

Author

Buyck, Bart, Zoller, Stefan, and Hofstetter, Valerie

Abstract

For the very first time, morpho-anatomical features of both fruiting bodies as well as below-ground structures have been confronted with a newly produced multigene phylogeny of root symbiotic basidiomycetes using one of the most speciose genera of ectomycorrhizal fungi (Russula, Russulales) as an example. In this first of two papers, the authors focus more specifically on below-ground structures. Our five-gene phylogeny divides the genus in five main clades, here interpreted as representing seven subgenera, all significantly supported. Although more conserved than features of fruiting bodies, the anatomy of ectomycorrhiza does not allow for an unambiguous characterization of the main clades resolved by phylogenetic analysis, but the anatomy of ectomycorrhiza performs better to naturally classify the species of this genus. Features of fruiting bodies remain much more adequate for the delimitation of terminal clades and are irreplaceable for morphological species identification. Tropical taxa mostly nest in ancient lineages, but are also present in some terminal clades of otherwise temperate species groups. The shift from plectenchymatic to pseudoparenchymatic ECM outer mantle structures happened most likely already in the paleotropics, and is here hypothesized to have facilitated a major diversification of the genus with new hosts in the northern hemisphere. Available data as well as our own observations on below ground structures of several Lactifluus species suggests that this genus shares with Russula the absence of lactifers in ECM mantles and rhizomorphs, contrary to species of Lactarius where lactifers are always present. First observations on rhizomorphs of species in Multifurca confirm the presence of vessel-like and ladder-like hyphae, also found in the other agarioid genera of this family, while distinct lactifers are only present in the lactarioid, but not in russuloid members of this genus. [ABSTRACT FROM AUTHOR]

Published
2018
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12. The Faces of Fungi database: fungal names linked with morphology, phylogeny and human impacts

Author

Jayasiri, Subashini C., primary, Hyde, Kevin D., additional, Ariyawansa, Hiran A., additional, Bhat, Jayarama, additional, Buyck, Bart, additional, Cai, Lei, additional, Dai, Yu-Cheng, additional, Abd-Elsalam, Kamel A., additional, Ertz, Damien, additional, Hidayat, Iman, additional, Jeewon, Rajesh, additional, Jones, E. B. Gareth, additional, Bahkali, Ali H., additional, Karunarathna, Samantha C., additional, Liu, Jian-Kui, additional, Luangsa-ard, J. Jennifer, additional, Lumbsch, H. Thorsten, additional, Maharachchikumbura, Sajeewa S. N., additional, McKenzie, Eric H. C., additional, Moncalvo, Jean-Marc, additional, Ghobad-Nejhad, Masoomeh, additional, Nilsson, Henrik, additional, Pang, Ka-Lai, additional, Pereira, Olinto L., additional, Phillips, Alan J. L., additional, Raspé, Olivier, additional, Rollins, Adam W., additional, Romero, Andrea I., additional, Etayo, Javier, additional, Selçuk, Faruk, additional, Stephenson, Steven L., additional, Suetrong, Satinee, additional, Taylor, Joanne E., additional, Tsui, Clement K. M., additional, Vizzini, Alfredo, additional, Abdel-Wahab, Mohamed A., additional, Wen, Ting-Chi, additional, Boonmee, Saranyaphat, additional, Dai, Dong Qin, additional, Daranagama, Dinushani A., additional, Dissanayake, Asha J., additional, Ekanayaka, Anusha H., additional, Fryar, S. C., additional, Hongsanan, Sinang, additional, Jayawardena, Ruvishika S., additional, Li, Wen-Jing, additional, Perera, Rekhani H., additional, Phookamsak, R., additional, de Silva, Nimali I., additional, Thambugala, Kasun M., additional, Tian, Qing, additional, Wijayawardene, Nalin N., additional, Zhao, Rui-Lin, additional, Zhao, Qi, additional, Kang, Ji-Chuan, additional, and Promputtha, Itthayakorn, additional

Published
2015
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13. Fungal diversity notes 1–110: taxonomic and phylogenetic contributions to fungal species

Author

Liu, Jian Kui, primary, Hyde, Kevin D., additional, Jones, E. B. Gareth, additional, Ariyawansa, Hiran A., additional, Bhat, Darbhe J., additional, Boonmee, Saranyaphat, additional, Maharachchikumbura, Sajeewa S. N., additional, McKenzie, Eric H. C., additional, Phookamsak, Rungtiwa, additional, Phukhamsakda, Chayanard, additional, Shenoy, Belle Damodara, additional, Abdel-Wahab, Mohamed A., additional, Buyck, Bart, additional, Chen, Jie, additional, Chethana, K. W. Thilini, additional, Singtripop, Chonticha, additional, Dai, Dong Qin, additional, Dai, Yu Cheng, additional, Daranagama, Dinushani A., additional, Dissanayake, Asha J., additional, Doilom, Mingkwan, additional, D’souza, Melvina J., additional, Fan, Xin Lei, additional, Goonasekara, Ishani D., additional, Hirayama, Kazuyuki, additional, Hongsanan, Sinang, additional, Jayasiri, Subashini C., additional, Jayawardena, Ruvishika S., additional, Karunarathna, Samantha C., additional, Li, Wen Jing, additional, Mapook, Ausana, additional, Norphanphoun, Chada, additional, Pang, Ka Lai, additional, Perera, Rekhani H., additional, Peršoh, Derek, additional, Pinruan, Umpava, additional, Senanayake, Indunil C., additional, Somrithipol, Sayanh, additional, Suetrong, Satinee, additional, Tanaka, Kazuaki, additional, Thambugala, Kasun M., additional, Tian, Qing, additional, Tibpromma, Saowaluck, additional, Udayanga, Danushka, additional, Wijayawardene, Nalin N., additional, Wanasinghe, Dhanuska, additional, Wisitrassameewong, Komsit, additional, Zeng, Xiang Yu, additional, Abdel-Aziz, Faten A., additional, Adamčík, Slavomir, additional, Bahkali, Ali H., additional, Boonyuen, Nattawut, additional, Bulgakov, Timur, additional, Callac, Philippe, additional, Chomnunti, Putarak, additional, Greiner, Katrin, additional, Hashimoto, Akira, additional, Hofstetter, Valerie, additional, Kang, Ji Chuan, additional, Lewis, David, additional, Li, Xing Hong, additional, Liu, Xing Zhong, additional, Liu, Zuo Yi, additional, Matsumura, Misato, additional, Mortimer, Peter E., additional, Rambold, Gerhard, additional, Randrianjohany, Emile, additional, Sato, Genki, additional, Sri-Indrasutdhi, Veera, additional, Tian, Cheng Ming, additional, Verbeken, Annemieke, additional, von Brackel, Wolfgang, additional, Wang, Yong, additional, Wen, Ting Chi, additional, Xu, Jian Chu, additional, Yan, Ji Ye, additional, Zhao, Rui Lin, additional, and Camporesi, Erio, additional

Published
2015
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15. Cantharellus (Cantharellales, Basidiomycota) revisited in Europe through a multigene phylogeny.

Author

Olariaga, Ibai, Moreno, Gabriel, Manjón, Jose, Salcedo, Isabel, Hofstetter, Valérie, Rodríguez, Diego, and Buyck, Bart

Abstract

Resolving species delimitation issues of European Cantharellus is crucial to correctly name chanterelles around the globe. Thirty names referring to Cantharellus s. str. have been described in Europe, some of which are used in other continents. Based on combined analyses of ITS2, LSU, RPB2 and TEF-1, merely eight species are here recognized in Europe applying the genealogical concordance phylogenetic species recognition criteria, one of which, C. roseofagetorum, is described as new. Morphological characters used in species delimitation are mapped and their variability evaluated. The colour of the hymenophore in young specimens is found to be a rather constant morphological character of taxonomic use. European species of Cantharellus are morphologically distinguished by unique combinations of characters, such as the presence of a pink pileal coating, pileus and hymenophore colour when young, and in some cases, the mean spore length and ecology. Eighteen type specimens from Europe are sequenced. Based on revised species concepts sixteen novel taxonomic synonyms are here proposed for European chanterelles: C. alborufescens (= C. henrici, C. ilicis, C. lilacinopruinatus), C. amethysteus (= C. cibarius subsp. squamulosus, C. cibarius var. umbrinus, C. rufipes), C. cibarius (= C. cibarius var. atlanticus, C. parviluteus), C. ferruginascens (= C. cibarius var. flavipes), C. friesii (= C. ignescens), C. pallens (= C. cibarius var. albidus, C. cibarius var. bicolor, C. subpruinosus), and C. romagnesianus (= C. pseudominimus, C. lourizanianus, C. romagnesianus var. parvisporus). The type of Cantharellus, C. cibarius, is epitypified. Descriptions, colour illustrations and a key to all European species are provided. [ABSTRACT FROM AUTHOR]

Published
2017
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17. Fungal diversity notes 111-252-taxonomic and phylogenetic contributions to fungal taxa.

Author

Ariyawansa, Hiran, Hyde, Kevin, Jayasiri, Subashini, Buyck, Bart, Chethana, K., Dai, Dong, Dai, Yu, Daranagama, Dinushani, Jayawardena, Ruvishika, Lücking, Robert, Ghobad-Nejhad, Masoomeh, Niskanen, Tuula, Thambugala, Kasun, Voigt, Kerstin, Zhao, Rui, Li, Guo-Jie, Doilom, Mingkwan, Boonmee, Saranyaphat, Yang, Zhu, and Cai, Qing

Abstract

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. The new families, Ascocylindricaceae, Caryosporaceae and Wicklowiaceae (Ascomycota) are introduced based on their distinct lineages and unique morphology. The new Dothideomycete genera Pseudomassariosphaeria ( Amniculicolaceae), Heracleicola, Neodidymella and Pseudomicrosphaeriopsis ( Didymellaceae), Pseudopithomyces ( Didymosphaeriaceae), Brunneoclavispora, Neolophiostoma and Sulcosporium ( Halotthiaceae), Lophiohelichrysum ( Lophiostomataceae), Galliicola, Populocrescentia and Vagicola ( Phaeosphaeriaceae), Ascocylindrica ( Ascocylindricaceae), Elongatopedicellata ( Roussoellaceae), Pseudoasteromassaria ( Latoruaceae) and Pseudomonodictys ( Macrodiplodiopsidaceae) are introduced. The newly described species of Dothideomycetes (Ascomycota) are Pseudomassariosphaeria bromicola ( Amniculicolaceae), Flammeascoma lignicola ( Anteagloniaceae), Ascocylindrica marina ( Ascocylindricaceae), Lembosia xyliae ( Asterinaceae), Diplodia crataegicola and Diplodia galiicola ( Botryosphaeriaceae), Caryospora aquatica ( Caryosporaceae), Heracleicola premilcurensis and Neodidymella thailandicum ( Didymellaceae), Pseudopithomyces palmicola ( Didymosphaeriaceae), Floricola viticola ( Floricolaceae), Brunneoclavispora bambusae, Neolophiostoma pigmentatum and Sulcosporium thailandica ( Halotthiaceae), Pseudoasteromassaria fagi ( Latoruaceae), Keissleriella dactylidicola ( Lentitheciaceae), Lophiohelichrysum helichrysi ( Lophiostomataceae), Aquasubmersa japonica ( Lophiotremataceae), Pseudomonodictys tectonae ( Macrodiplodiopsidaceae), Microthyrium buxicola and Tumidispora shoreae ( Microthyriaceae), Alloleptosphaeria clematidis, Allophaeosphaeria cytisi, Allophaeosphaeria subcylindrospora, Dematiopleospora luzulae, Entodesmium artemisiae, Galiicola pseudophaeosphaeria, Loratospora luzulae, Nodulosphaeria senecionis, Ophiosphaerella aquaticus, Populocrescentia forlicesenensis and Vagicola vagans ( Phaeosphaeriaceae), Elongatopedicellata lignicola, Roussoella magnatum and Roussoella angustior ( Roussoellaceae) and Shrungabeeja longiappendiculata ( Tetraploasphaeriaceae). The new combinations Pseudomassariosphaeria grandispora, Austropleospora archidendri, Pseudopithomyces chartarum, Pseudopithomyces maydicus, Pseudopithomyces sacchari, Vagicola vagans, Punctulariopsis cremeoalbida and Punctulariopsis efibulata Dothideomycetes. The new genera Dictyosporella ( Annulatascaceae), and Tinhaudeus ( Halosphaeriaceae) are introduced in Sordariomycetes (Ascomycota) while Dictyosporella aquatica ( Annulatascaceae), Chaetosphaeria rivularia ( Chaetosphaeriaceae), Beauveria gryllotalpidicola and Beauveria loeiensis ( Cordycipitaceae), Seimatosporium sorbi and Seimatosporium pseudorosarum ( Discosiaceae), Colletotrichum aciculare, Colletotrichum fusiforme and Colletotrichum hymenocallidicola ( Glomerellaceae), Tinhaudeus formosanus ( Halosphaeriaceae), Pestalotiopsis subshorea and Pestalotiopsis dracaenea ( Pestalotiopsiceae), Phaeoacremonium tectonae ( Togniniaceae), Cytospora parasitica and Cytospora tanaitica ( Valsaceae), Annulohypoxylon palmicola, Biscogniauxia effusae and Nemania fusoideis ( Xylariaceae) are introduced as novel species to order Sordariomycetes. The newly described species of Eurotiomycetes are Mycocalicium hyaloparvicellulum ( Mycocaliciaceae). Acarospora septentrionalis and Acarospora castaneocarpa ( Acarosporaceae), Chapsa multicarpa and Fissurina carassensis ( Graphidaceae), Sticta fuscotomentosa and Sticta subfilicinella ( Lobariaceae) are newly introduced in class Lecanoromycetes. In class Pezizomycetes, Helvella pseudolacunosa and Helvella rugosa ( Helvellaceae) are introduced as new species. The new families, Dendrominiaceae and Neoantrodiellaceae (Basidiomycota) are introduced together with a new genus Neoantrodiella ( Neoantrodiellaceae), here based on both morphology coupled with molecular data. In the class Agaricomycetes, Agaricus pseudolangei, Agaricus haematinus, Agaricus atrodiscus and Agaricus exilissimus ( Agaricaceae), Amanita melleialba, Amanita pseudosychnopyramis and Amanita subparvipantherina ( Amanitaceae), Entoloma calabrum, Cora barbulata, Dictyonema gomezianum and Inocybe granulosa ( Inocybaceae), Xerocomellus sarnarii ( Boletaceae), Cantharellus eucalyptorum, Cantharellus nigrescens, Cantharellus tricolor and Cantharellus variabilicolor ( Cantharellaceae), Cortinarius alboamarescens, Cortinarius brunneoalbus, Cortinarius ochroamarus, Cortinarius putorius and Cortinarius seidlii ( Cortinariaceae), Hymenochaete micropora and Hymenochaete subporioides ( Hymenochaetaceae), Xylodon ramicida ( Schizoporaceae), Colospora andalasii ( Polyporaceae), Russula guangxiensis and Russula hakkae ( Russulaceae), Tremella dirinariae, Tremella graphidis and Tremella pyrenulae ( Tremellaceae) are introduced. Four new combinations Neoantrodiella gypsea, Neoantrodiella thujae ( Neoantrodiellaceae), Punctulariopsis cremeoalbida, Punctulariopsis efibulata ( Punctulariaceae) are also introduced here for the division Basidiomycota. Furthermore Absidia caatinguensis, Absidia koreana and Gongronella koreana ( Cunninghamellaceae), Mortierella pisiformis and Mortierella formosana ( Mortierellaceae) are newly introduced in the Zygomycota, while Neocallimastix cameroonii and Piromyces irregularis ( Neocallimastigaceae) are introduced in the Neocallimastigomycota. Reference specimens or changes in classification and notes are provided for Alternaria ethzedia, Cucurbitaria ephedricola, Austropleospora, Austropleospora archidendri, Byssosphaeria rhodomphala, Lophiostoma caulium, Pseudopithomyces maydicus, Massariosphaeria, Neomassariosphaeria and Pestalotiopsis montellica. [ABSTRACT FROM AUTHOR]

Published
2015
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21. Sequence data reveal a high diversity of Cantharellus associated with endemic vegetation in Madagascar.

Author

Buyck, Bart, Kauff, Frank, Randrianjohany, Emile, and Hofstetter, Valérie

Abstract

This revision of Cantharellus in Madagascar deals with species that are associated with strictly endemic host trees and shrubs. Based on morphological differences and molecular sequence data of the tef-1 gene, five new species are proposed ( C. albidolutescens, C. ambohitantelyensis, C. ibityensis, C. paucifurcatus and C. sebosus), as well as one new subspecies, C. subincarnatus ssp. rubrosalmoneus, whereas C. decolorans and C. platyphyllus ssp. bojeriensis are epitypified. A key is provided to all Cantharellus that grow with native vegetation in Madagascar. [ABSTRACT FROM AUTHOR]

Published
2015
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22. A multilocus phylogeny for worldwide Cantharellus (Cantharellales, Agaricomycetidae).

Author

Buyck, Bart, Kauff, Frank, Eyssartier, Guillaume, Couloux, André, and Hofstetter, Valérie

Abstract

After a short historical overview of past systematic studies on Cantharellus, discussing delimitation and species diversity of the genus as well as previous, morphology-based, infrageneric classifications, this paper presents the first molecularly-based infrageneric classification of this genus using a multigene phylogenetic approach (nucLSU, mitSSU, RPB2 and tef-1) on a dataset that covers approximately halve of the described chanterelles worldwide, including many type specimens. Six subgenera are recognized and the recognition of subgenus Afrocantharellus as a separate genus is not accepted. The taxonomic value of individual morphological features is discussed as challenged by this new multigene phylogeny which comprises five new sections, one new subgenus and many emendations for previously recognized infrageneric groups. The paper discusses the observed discrepancy in biodiversity of Cantharellus when comparing between studies that focus either on below- or above-ground presence. A preliminary biogeographic hypothesis suggests an 'out of Africa' Gondwanan origin as a result of vicariance and subsequent migrations. [ABSTRACT FROM AUTHOR]

Published
2014
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23. Myxomycetes from Papua New Guinea and New Caledonia.

Author

Kylin, Henrik, Mitchell, David, Seraoui, El-Hacène, and Buyck, Bart

Abstract

We present a compilation of all myxomycetes recorded from Papua New Guinea (PNG) and New Caledonia (NC). Specimens were collected during field trips in September 1983-January 1984 to both territories and in August 1991, October 2007, and April 2009 to NC. Bark and dung samples for moist chamber cultures were collected during the field trips in September 1983-January 1984 (PNG and NC) and in August 1991 and October 2007 (NC). In addition, information from previous publications and unpublished specimens in the herbarium at the Plant Protection Instituted in Port Moresby, PNG, are included. A total of 180 species are reported. Of the 63 species from PNG 51 are new to the country, and 123 of the 149 species from NC are new to the territory. [ABSTRACT FROM AUTHOR]

Published
2013
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24. Molecular evidence for novel Cantharellus (Cantharellales, Basidiomycota) from tropical African miombo woodland and a key to all tropical African chanterelles.

Author

Buyck, Bart, Kauff, Frank, Cruaud, Corinne, and Hofstetter, Valérie

Abstract

The authors present a combined morphological and molecular approach of the genus Cantharellus in Africa. Morphological descriptions and detailed illustrations are provided for five new species from the Zambezian savannah woodlands in tropical Africa: C. afrocibarius, C. gracilis, C. humidicolus, C. miomboensis and C. tanzanicus. A maximum likelihood analysis of tef-1 sequences obtained for 83 collections of Cantharellus that are representative of all major groups in world wide Cantharellus, places a total of 13 African chanterelles, including the five newly described taxa. The recognition of a separate genus Afrocantharellus is rejected. An identification key based on the re-examination of all existing type material is provided for all presently known African Cantharellus. [ABSTRACT FROM AUTHOR]

Published
2013
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