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Danushka S. Tennakoon

Bio: Danushka S. Tennakoon is an academic researcher from Mae Fah Luang University. The author has contributed to research in topics: Dothideomycetes & Pleosporales. The author has an hindex of 13, co-authored 31 publications receiving 1011 citations. Previous affiliations of Danushka S. Tennakoon include National Chiayi University & Kunming Institute of Botany.

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Journal ArticleDOI
TL;DR: This manuscript reviews fifty ways in which fungi can potentially be utilized as biotechnology and provides a flow chart that can be used to convince funding bodies of the importance of fungi for biotechnological research and as potential products.
Abstract: Fungi are an understudied, biotechnologically valuable group of organisms. Due to the immense range of habitats that fungi inhabit, and the consequent need to compete against a diverse array of other fungi, bacteria, and animals, fungi have developed numerous survival mechanisms. The unique attributes of fungi thus herald great promise for their application in biotechnology and industry. Moreover, fungi can be grown with relative ease, making production at scale viable. The search for fungal biodiversity, and the construction of a living fungi collection, both have incredible economic potential in locating organisms with novel industrial uses that will lead to novel products. This manuscript reviews fifty ways in which fungi can potentially be utilized as biotechnology. We provide notes and examples for each potential exploitation and give examples from our own work and the work of other notable researchers. We also provide a flow chart that can be used to convince funding bodies of the importance of fungi for biotechnological research and as potential products. Fungi have provided the world with penicillin, lovastatin, and other globally significant medicines, and they remain an untapped resource with enormous industrial potential.

404 citations

Journal ArticleDOI
Rungtiwa Phookamsak, Kevin D. Hyde, Rajesh Jeewon1, D. Jayarama Bhat, E. B. Gareth Jones2, E. B. Gareth Jones3, Sajeewa S. N. Maharachchikumbura4, Olivier Raspé5, Samantha C. Karunarathna6, Samantha C. Karunarathna7, Dhanushka N. Wanasinghe, Sinang Hongsanan8, Sinang Hongsanan9, Mingkwan Doilom, Danushka S. Tennakoon, A. R. Machado10, A. L. Firmino11, Aniket Ghosh12, Anuruddha Karunarathna, Armin Mešić, Arun Kumar Dutta13, Benjarong Thongbai, B. Devadatha14, Chada Norphanphoun, Chanokned Senwanna2, Chanokned Senwanna9, De-Ping Wei, Dhandevi Pem8, Dhandevi Pem9, Frank K. Ackah15, Gen-Nuo Wang16, Hong-Bo Jiang6, Hong-Bo Jiang9, Hugo Madrid17, Hyang Burm Lee18, Ishani D. Goonasekara9, Ishani D. Goonasekara6, Ishara S. Manawasinghe9, I. Kusan, Josep Cano, Josepa Gené, Junfu Li6, Junfu Li9, Kanad Das19, Krishnendu Acharya13, K. N. Anil Raj20, K. P. Deepna Latha20, K. W. Thilini Chethana9, Mao-Qiang He21, Margarita Dueñas22, M. Jadan, María P. Martín22, Milan C. Samarakoon9, Milan C. Samarakoon2, Monika C. Dayarathne9, Monika C. Dayarathne6, Mubashar Raza21, Myung Soo Park23, M. Teresa Telleria22, Napalai Chaiwan6, Napalai Chaiwan9, Neven Matočec, Nimali I. de Silva, Olinto Liparini Pereira24, Paras Nath Singh25, Patinjareveettil Manimohan20, Priyanka Uniyal12, Qiu-Ju Shang9, Rajendra P. Bhatt12, Rekhani H. Perera9, Renato Lúcio Mendes Alvarenga10, Sandra Nogal-Prata22, Sanjay K. Singh25, Santhiti Vadthanarat2, Seung-Yoon Oh23, Shi-Ke Huang, Shiwali Rana25, Sirinapa Konta9, Sirinapa Konta6, Soumitra Paloi13, Subashini C. Jayasiri9, Subashini C. Jayasiri6, Sun Jeong Jeon18, Tahir Mehmood12, Tatiana Baptista Gibertoni10, Thuong T. T. Nguyen18, Upendra Singh12, Vinodhini Thiyagaraja, V. Venkateswara Sarma14, Wei Dong, Xian-Dong Yu16, Yong-Zhong Lu9, Yong-Zhong Lu26, Young Woon Lim23, Yun Chen, Zdenko Tkalčec, Zhi-Feng Zhang21, Zong-Long Luo27, Zong-Long Luo9, Dinushani A. Daranagama28, Kasun M. Thambugala29, Saowaluck Tibpromma, Erio Camporesi, Timur S. Bulgakov, Asha J. Dissanayake9, Indunil C. Senanayake9, Indunil C. Senanayake8, Dong-Qin Dai, Li-Zhou Tang, Sehroon Khan6, Sehroon Khan7, Huang Zhang16, Itthayakorn Promputtha2, Lei Cai21, Putarak Chomnunti9, Rui-Lin Zhao21, Saisamorn Lumyong2, Saranyaphat Boonmee9, Ting-Chi Wen26, Peter E. Mortimer6, Jianchu Xu7 
TL;DR: The present study describes 12 new genera, 74 new species, three new combinations, two reference specimens, a re-circumscription of the epitype, and 15 records of sexual-asexual morph connections, new hosts and new geographical distributions.
Abstract: This article is the ninth in the series of Fungal Diversity Notes, where 107 taxa distributed in three phyla, nine classes, 31 orders and 57 families are described and illustrated. Taxa described in the present study include 12 new genera, 74 new species, three new combinations, two reference specimens, a re-circumscription of the epitype, and 15 records of sexual-asexual morph connections, new hosts and new geographical distributions. Twelve new genera comprise Brunneofusispora, Brunneomurispora, Liua, Lonicericola, Neoeutypella, Paratrimmatostroma, Parazalerion, Proliferophorum, Pseudoastrosphaeriellopsis, Septomelanconiella, Velebitea and Vicosamyces. Seventy-four new species are Agaricus memnonius, A. langensis, Aleurodiscus patagonicus, Amanita flavoalba, A. subtropicana, Amphisphaeria mangrovei, Baorangia major, Bartalinia kunmingensis, Brunneofusispora sinensis, Brunneomurispora lonicerae, Capronia camelliae-yunnanensis, Clavulina thindii, Coniochaeta simbalensis, Conlarium thailandense, Coprinus trigonosporus, Liua muriformis, Cyphellophora filicis, Cytospora ulmicola, Dacrymyces invisibilis, Dictyocheirospora metroxylonis, Distoseptispora thysanolaenae, Emericellopsis koreana, Galiicola baoshanensis, Hygrocybe lucida, Hypoxylon teeravasati, Hyweljonesia indica, Keissleriella caraganae, Lactarius olivaceopallidus, Lactifluus midnapurensis, Lembosia brigadeirensis, Leptosphaeria urticae, Lonicericola hyaloseptispora, Lophiotrema mucilaginosis, Marasmiellus bicoloripes, Marasmius indojasminodorus, Micropeltis phetchaburiensis, Mucor orantomantidis, Murilentithecium lonicerae, Neobambusicola brunnea, Neoeutypella baoshanensis, Neoroussoella heveae, Neosetophoma lonicerae, Ophiobolus malleolus, Parabambusicola thysanolaenae, Paratrimmatostroma kunmingensis, Parazalerion indica, Penicillium dokdoense, Peroneutypa mangrovei, Phaeosphaeria cycadis, Phanerochaete australosanguinea, Plectosphaerella kunmingensis, Plenodomus artemisiae, P. lijiangensis, Proliferophorum thailandicum, Pseudoastrosphaeriellopsis kaveriana, Pseudohelicomyces menglunicus, Pseudoplagiostoma mangiferae, Robillarda mangiferae, Roussoella elaeicola, Russula choptae, R. uttarakhandia, Septomelanconiella thailandica, Spencermartinsia acericola, Sphaerellopsis isthmospora, Thozetella lithocarpi, Trechispora echinospora, Tremellochaete atlantica, Trichoderma koreanum, T. pinicola, T. rugulosum, Velebitea chrysotexta, Vicosamyces venturisporus, Wojnowiciella kunmingensis and Zopfiella indica. Three new combinations are Baorangia rufomaculata, Lanmaoa pallidorosea and Wojnowiciella rosicola. The reference specimens of Canalisporium kenyense and Tamsiniella labiosa are designated. The epitype of Sarcopeziza sicula is re-circumscribed based on cyto- and histochemical analyses. The sexual-asexual morph connection of Plenodomus sinensis is reported from ferns and Cirsium for the first time. In addition, the new host records and country records are Amanita altipes, A. melleialba, Amarenomyces dactylidis, Chaetosphaeria panamensis, Coniella vitis, Coprinopsis kubickae, Dothiorella sarmentorum, Leptobacillium leptobactrum var. calidus, Muyocopron lithocarpi, Neoroussoella solani, Periconia cortaderiae, Phragmocamarosporium hederae, Sphaerellopsis paraphysata and Sphaeropsis eucalypticola.

171 citations

Journal ArticleDOI
Kevin D. Hyde, Chada Norphanphoun, V.P. Abreu1, Anna L. Bazzicalupo2, K. W. Thilini Chethana3, Marco Clericuzio4, Monika C. Dayarathne3, Asha J. Dissanayake3, Anusha H. Ekanayaka5, Anusha H. Ekanayaka3, Mao-Qiang He6, Mao-Qiang He7, Mao-Qiang He3, Sinang Hongsanan3, Shi-Ke Huang3, Subashini C. Jayasiri, Ruvishika S. Jayawardena3, Anuruddha Karunarathna, Sirinapa Konta3, I. Kusan, Hyun Lee8, Junfu Li3, Chuan-Gen Lin3, Ning-Guo Liu, Yong-Zhong Lu, Zong-Long Luo3, Zong-Long Luo9, Ishara S. Manawasinghe3, Ausana Mapook, Rekhani H. Perera, Rungtiwa Phookamsak3, Rungtiwa Phookamsak10, Rungtiwa Phookamsak5, Chayanard Phukhamsakda, Igor Siedlecki11, Adriene Mayra Soares12, Danushka S. Tennakoon3, Qing Tian3, Saowaluck Tibpromma, Dhanushka N. Wanasinghe, Yuan-Pin Xiao, Jing Yang, Xiang-Yu Zeng3, Xiang-Yu Zeng13, Faten A. Abdel-Aziz14, Wen-Jing Li, Indunil C. Senanayake, Qiu-Ju Shang3, Dinushani A. Daranagama3, Nimali I. de Silva, Kasun M. Thambugala, Mohamed A. Abdel-Wahab14, Ali H. Bahkali15, Mary L. Berbee2, Saranyaphat Boonmee3, D. Jayarama Bhat16, Timur S. Bulgakov, Bart Buyck17, Erio Camporesi, Rafael F. Castañeda-Ruiz, Putarak Chomnunti3, Minkwan Doilom3, Francesco Dovana18, Tatiana Baptista Gibertoni12, M. Jadan, Rajesh Jeewon19, E. B. Gareth Jones, Ji-Chuan Kang13, Samantha C. Karunarathna10, Samantha C. Karunarathna5, Young Woon Lim8, Jian-Kui Liu, Zuo-Yi Liu, Helio Longoni Plautz, Saisamorn Lumyong6, Sajeewa S. N. Maharachchikumbura20, Neven Matočec, Eric H. C. McKenzie21, Armin Mešić, Daniel Miller, Julia Pawłowska11, Olinto Liparini Pereira1, Itthayakorn Promputtha3, Itthayakorn Promputtha6, Andrea Irene Romero22, Andrea Irene Romero23, Leif Ryvarden24, Hong-Yan Su9, Satinee Suetrong25, Zdenko Tkalčec, Alfredo Vizzini18, Ting-Chi Wen13, Komsit Wisitrassameewong8, Marta Wrzosek11, J. C. Xu3, J. C. Xu5, J. C. Xu10, Qi Zhao5, Rui-Lin Zhao7, Peter E. Mortimer5, Peter E. Mortimer7 
TL;DR: This study introduces a new family Fuscostagonosporaceae in Dothideomycetes and introduces the new ascomycete genera Acericola, Castellaniomyces, Dictyosporina and Longitudinalis.
Abstract: This is the sixth in a series of papers where we bring collaborating mycologists together to produce a set of notes of several taxa of fungi. In this study we introduce a new family Fuscostagonosporaceae in Dothideomycetes. We also introduce the new ascomycete genera Acericola, Castellaniomyces, Dictyosporina and Longitudinalis and new species Acericola italica, Alternariaster trigonosporus, Amarenomyces dactylidis, Angustimassarina coryli, Astrocystis bambusicola, Castellaniomyces rosae, Chaetothyrina artocarpi, Chlamydotubeufia krabiensis, Colletotrichum lauri, Collodiscula chiangraiensis, Curvularia palmicola, Cytospora mali-sylvestris, Dictyocheirospora cheirospora, Dictyosporina ferruginea, Dothiora coronillae, Dothiora spartii, Dyfrolomyces phetchaburiensis, Epicoccum cedri, Epicoccum pruni, Fasciatispora calami, Fuscostagonospora cytisi, Grandibotrys hyalinus, Hermatomyces nabanheensis, Hongkongmyces thailandica, Hysterium rhizophorae, Jahnula guttulaspora, Kirschsteiniothelia rostrata, Koorchalomella salmonispora, Longitudinalis nabanheensis, Lophium zalerioides, Magnibotryascoma mali, Meliola clerodendri-infortunati, Microthyrium chinense, Neodidymelliopsis moricola, Neophaeocryptopus spartii, Nigrograna thymi, Ophiocordyceps cossidarum, Ophiocordyceps issidarum, Ophiosimulans plantaginis, Otidea pruinosa, Otidea stipitata, Paucispora kunmingense, Phaeoisaria microspora, Pleurothecium floriforme, Poaceascoma halophila, Periconia aquatica, Periconia submersa, Phaeosphaeria acaciae, Phaeopoacea muriformis, Pseudopithomyces kunmingnensis, Ramgea ozimecii, Sardiniella celtidis, Seimatosporium italicum, Setoseptoria scirpi, Torula gaodangensis and Vamsapriya breviconidiophora. We also provide an amended account of Rhytidhysteron to include apothecial ascomata and a J+ hymenium. The type species of Ascotrichella hawksworthii (Xylariales genera incertae sedis), Biciliopsis leptogiicola (Sordariomycetes genera incertae sedis), Brooksia tropicalis (Micropeltidaceae), Bryochiton monascus (Teratosphaeriaceae), Bryomyces scapaniae (Pseudoperisporiaceae), Buelliella minimula (Dothideomycetes genera incertae sedis), Carinispora nypae (Pseudoastrosphaeriellaceae), Cocciscia hammeri (Verrucariaceae), Endoxylina astroidea (Diatrypaceae), Exserohilum turcicum (Pleosporaceae), Immotthia hypoxylon (Roussoellaceae), Licopolia franciscana (Vizellaceae), Murispora rubicunda (Amniculicolaceae) and Doratospora guianensis (synonymized under Rizalia guianensis, Trichosphaeriaceae) were re-examined and descriptions, illustrations and discussion on their familial placement are given based on phylogeny and morphological data. New host records or new country reports are provided for Chlamydotubeufia huaikangplaensis, Colletotrichum fioriniae, Diaporthe subclavata, Diatrypella vulgaris, Immersidiscosia eucalypti, Leptoxyphium glochidion, Stemphylium vesicarium, Tetraploa yakushimensis and Xepicula leucotricha. Diaporthe baccae is synonymized under Diaporthe rhusicola. A reference specimen is provided for Periconia minutissima. Updated phylogenetic trees are provided for most families and genera. We introduce the new basidiomycete species Agaricus purpurlesquameus, Agaricus rufusfibrillosus, Lactifluus holophyllus, Lactifluus luteolamellatus, Lactifluus pseudohygrophoroides, Russula benwooii, Russula hypofragilis, Russula obscurozelleri, Russula parapallens, Russula phoenicea, Russula pseudopelargonia, Russula pseudotsugarum, Russula rhodocephala, Russula salishensis, Steccherinum amapaense, Tephrocybella constrictospora, Tyromyces amazonicus and Tyromyces angulatus and provide updated trees to the genera. We also introduce Mortierella formicae in Mortierellales, Mucoromycota and provide an updated phylogenetic tree.

160 citations

Journal ArticleDOI
TL;DR: Novel fungal taxa are described in the present study, including 17 new genera, 93 new species, four combinations, a sexual record for a species and new host records for 16 species.
Abstract: This paper is the seventh in the Fungal Diversity Notes series, where 131 taxa accommodated in 28 families are mainly described from Rosa (Rosaceae) and a few other hosts. Novel fungal taxa are described in the present study, including 17 new genera, 93 new species, four combinations, a sexual record for a species and new host records for 16 species. Bhatiellae, Cycasicola, Dactylidina, Embarria, Hawksworthiana, Italica, Melanocucurbitaria, Melanodiplodia, Monoseptella, Uzbekistanica, Neoconiothyrium, Neopaucispora, Pararoussoella, Paraxylaria, Marjia, Sporormurispora and Xenomassariosphaeria are introduced as new ascomycete genera. We also introduce the new species Absidia jindoensis, Alternaria doliconidium, A. hampshirensis, Angustimassarina rosarum, Astragalicola vasilyevae, Backusella locustae, Bartalinia rosicola, Bhatiellae rosae, Broomella rosae, Castanediella camelliae, Coelodictyosporium rosarum, Comoclathris rosae, C. rosarum, Comoclathris rosigena, Coniochaeta baysunika, C. rosae, Cycasicola goaensis, Dactylidina shoemakeri, Dematiopleospora donetzica, D. rosicola, D. salsolae, Diaporthe rosae, D. rosicola, Endoconidioma rosae-hissaricae, Epicoccum rosae, Hawksworthiana clematidicola, H. lonicerae, Italica achilleae, Keissleriella phragmiticola, K. rosacearum, K. rosae, K. rosarum, Lophiostoma rosae, Marjia tianschanica, M. uzbekistanica, Melanocucurbitaria uzbekistanica, Melanodiplodia tianschanica, Monoseptella rosae, Mucor fluvius, Muriformistrickeria rosae, Murilentithecium rosae, Neoascochyta rosicola, Neoconiothyrium rosae, Neopaucispora rosaecae, Neosetophoma rosarum, N. rosae, N. rosigena, Neostagonospora artemisiae, Ophiobolus artemisiicola, Paraconiothyrium rosae, Paraphaeosphaeria rosae, P. rosicola, Pararoussoella rosarum, Parathyridaria rosae, Paraxylaria rosacearum, Penicillium acidum, P. aquaticum, Phragmocamarosporium rosae, Pleospora rosae, P. rosae-caninae, Poaceicola agrostina, P. arundinicola, P. rosae, Populocrescentia ammophilae, P. rosae, Pseudocamarosporium pteleae, P. ulmi-minoris, Pseudocercospora rosae, Pseudopithomyces rosae, Pseudostrickeria rosae, Sclerostagonospora lathyri, S. rosae, S. rosicola, Seimatosporium rosigenum, S. rosicola, Seiridium rosarum, Setoseptoria arundelensis, S. englandensis, S. lulworthcovensis, Sigarispora agrostidis, S. caryophyllacearum, S. junci, S. medicaginicola, S. rosicola, S. scrophulariae, S. thymi, Sporormurispora atraphaxidis, S. pruni, Suttonomyces rosae, Umbelopsis sinsidoensis, Uzbekistanica rosae-hissaricae, U. yakutkhanika, Wojnowicia rosicola, Xenomassariosphaeria rosae. New host records are provided for Amandinea punctata, Angustimassarina quercicola, Diaporthe rhusicola, D. eres, D. foeniculina, D. rudis, Diplodia seriata, Dothiorella iberica, Lasiodiplodia theobromae, Lecidella elaeochroma, Muriformistrickeria rubi, Neofusicoccum australe, Paraphaeosphaeria michotii, Pleurophoma pleurospora, Sigarispora caulium and Teichospora rubriostiolata. The new combinations are Dactylidina dactylidis (=Allophaeosphaeria dactylidis), Embarria clematidis (=Allophaeosphaeria clematidis), Hawksworthiana alliariae (=Dematiopleospora alliariae) and Italica luzulae (=Dematiopleospora luzulae). This study also provides some insights into the diversity of fungi on Rosa species and especially those on Rosa spines that resulted in the characterisation of eight new genera, 45 new species, and nine new host records. We also collected taxa from Rosa stems and there was 31% (20/65) overlap with taxa found on stems with that on spines. Because of the limited and non-targeted sampling for comparison with collections from spines and stems of the same host and location, it is not possible to say that the fungi on spines of Rosa differ from those on stems. The study however, does illustrate how spines are interesting substrates with high fungal biodiversity. This may be because of their hard structure resulting in slow decay and hence are suitable substrates leading to fungal colonisation. All data presented herein are based on morphological examination of specimens, coupled with phylogenetic sequence data to better integrate taxa into appropriate taxonomic ranks and infer their evolutionary relationships.

151 citations

Journal ArticleDOI
Kevin D. Hyde, Yang Dong1, Rungtiwa Phookamsak, Rajesh Jeewon2, D. Jayarama Bhat, E. B. Gareth Jones3, E. B. Gareth Jones4, Ning-Guo Liu, Pranami D. Abeywickrama5, Ausana Mapook5, Ausana Mapook6, De-Ping Wei, Rekhani H. Perera7, Rekhani H. Perera5, Ishara S. Manawasinghe5, Dhandevi Pem5, Dhandevi Pem8, Digvijayini Bundhun5, Digvijayini Bundhun4, Anuruddha Karunarathna, Anusha H. Ekanayaka5, Anusha H. Ekanayaka9, Dan-Feng Bao5, Dan-Feng Bao10, Dan-Feng Bao4, Junfu Li, Milan C. Samarakoon, Napalai Chaiwan5, Napalai Chaiwan1, Chuan-Gen Lin5, Kunthida Phutthacharoen5, Kunthida Phutthacharoen9, Sheng-Nan Zhang4, Sheng-Nan Zhang5, Indunil C. Senanayake8, Ishani D. Goonasekara5, Kasun M. Thambugala11, Chayanard Phukhamsakda5, Danushka S. Tennakoon, Hong-Bo Jiang, Jing Yang, Ming Zeng, Naruemon Huanraluek5, Jian-Kui Liu12, Subodini N. Wijesinghe, Qing Tian5, Saowaluck Tibpromma9, Saowaluck Tibpromma13, Saowaluck Tibpromma14, Rashika S. Brahmanage5, Saranyaphat Boonmee5, Shi-Ke Huang, Vinodhini Thiyagaraja, Yong-Zhong Lu7, Ruvishika S. Jayawardena5, Wei Dong, Er-Fu Yang9, Er-Fu Yang13, Sanjay K. Singh15, Shiv Mohan Singh16, Shiwali Rana15, Sneha S. Lad15, Garima Anand17, B. Devadatha18, B. Devadatha5, M. Niranjan18, V. Venkateswara Sarma18, Kare Liimatainen19, Begoña Aguirre-Hudson19, Tuula Niskanen19, Andy Overall, Renato Lúcio Mendes Alvarenga20, Tatiana Baptista Gibertoni20, Walter P. Pfliegler21, Enikő Horváth21, Alexandra Imre21, Amanda Lucia Alves20, Ana Carla da Silva Santos20, Patricia Vieira Tiago20, Timur S. Bulgakov, Dhanushaka N. Wanasinghe9, Dhanushaka N. Wanasinghe13, Dhanushaka N. Wanasinghe14, Ali H. Bahkali3, Mingkwan Doilom13, Mingkwan Doilom14, Mingkwan Doilom9, Abdallah M. Elgorban3, Sajeewa S. N. Maharachchikumbura12, Kunhiraman C. Rajeshkumar15, Danny Haelewaters, Peter E. Mortimer13, Peter E. Mortimer9, Qi Zhao9, Saisamorn Lumyong4, Saisamorn Lumyong22, Jianchu Xu9, Jianchu Xu13, Jianchu Xu14, Jun Sheng1 
TL;DR: The present study describes two new families, 12 new genera, 82 new species, five new combinations and 25 new records on new hosts and new geographical distributions as well as sexual-asexual reports.
Abstract: Fungal diversity notes is one of the important journal series of fungal taxonomy that provide detailed descriptions and illustrations of new fungal taxa, as well as providing new information of fungal taxa worldwide. This article is the 11th contribution to the fungal diversity notes series, in which 126 taxa distributed in two phyla, six classes, 24 orders and 55 families are described and illustrated. Taxa in this study were mainly collected from Italy by Erio Camporesi and also collected from China, India and Thailand, as well as in some other European, North American and South American countries. Taxa described in the present study include two new families, 12 new genera, 82 new species, five new combinations and 25 new records on new hosts and new geographical distributions as well as sexual-asexual reports. The two new families are Eriomycetaceae (Dothideomycetes, family incertae sedis) and Fasciatisporaceae (Xylariales, Sordariomycetes). The twelve new genera comprise Bhagirathimyces (Phaeosphaeriaceae), Camporesiomyces (Tubeufiaceae), Eriocamporesia (Cryphonectriaceae), Eriomyces (Eriomycetaceae), Neomonodictys (Pleurotheciaceae), Paraloratospora (Phaeosphaeriaceae), Paramonodictys (Parabambusicolaceae), Pseudoconlarium (Diaporthomycetidae, genus incertae sedis), Pseudomurilentithecium (Lentitheciaceae), Setoapiospora (Muyocopronaceae), Srinivasanomyces (Vibrisseaceae) and Xenoanthostomella (Xylariales, genera incertae sedis). The 82 new species comprise Acremonium chiangraiense, Adustochaete nivea, Angustimassarina camporesii, Bhagirathimyces himalayensis, Brunneoclavispora camporesii, Camarosporidiella camporesii, Camporesiomyces mali, Camposporium appendiculatum, Camposporium multiseptatum, Camposporium septatum, Canalisporium aquaticium, Clonostachys eriocamporesiana, Clonostachys eriocamporesii, Colletotrichum hederiicola, Coniochaeta vineae, Conioscypha verrucosa, Cortinarius ainsworthii, Cortinarius aurae, Cortinarius britannicus, Cortinarius heatherae, Cortinarius scoticus, Cortinarius subsaniosus, Cytospora fusispora, Cytospora rosigena, Diaporthe camporesii, Diaporthe nigra, Diatrypella yunnanensis, Dictyosporium muriformis, Didymella camporesii, Diutina bernali, Diutina sipiczkii, Eriocamporesia aurantia, Eriomyces heveae, Ernakulamia tanakae, Falciformispora uttaraditensis, Fasciatispora cocoes, Foliophoma camporesii, Fuscostagonospora camporesii, Helvella subtinta, Kalmusia erioi, Keissleriella camporesiana, Keissleriella camporesii, Lanspora cylindrospora, Loratospora arezzoensis, Mariannaea atlantica, Melanographium phoenicis, Montagnula camporesii, Neodidymelliopsis camporesii, Neokalmusia kunmingensis, Neoleptosporella camporesiana, Neomonodictys muriformis, Neomyrmecridium guizhouense, Neosetophoma camporesii, Paraloratospora camporesii, Paramonodictys solitarius, Periconia palmicola, Plenodomus triseptatus, Pseudocamarosporium camporesii, Pseudocercospora maetaengensis, Pseudochaetosphaeronema kunmingense, Pseudoconlarium punctiforme, Pseudodactylaria camporesiana, Pseudomurilentithecium camporesii, Pseudotetraploa rajmachiensis, Pseudotruncatella camporesii, Rhexocercosporidium senecionis, Rhytidhysteron camporesii, Rhytidhysteron erioi, Septoriella camporesii, Setoapiospora thailandica, Srinivasanomyces kangrensis, Tetraploa dwibahubeeja, Tetraploa pseudoaristata, Tetraploa thrayabahubeeja, Torula camporesii, Tremateia camporesii, Tremateia lamiacearum, Uzbekistanica pruni, Verruconis mangrovei, Wilcoxina verruculosa, Xenoanthostomella chromolaenae and Xenodidymella camporesii. The five new combinations are Camporesiomyces patagoniensis, Camporesiomyces vaccinia, Camposporium lycopodiellae, Paraloratospora gahniae and Rhexocercosporidium microsporum. The 22 new records on host and geographical distribution comprise Arthrinium marii, Ascochyta medicaginicola, Ascochyta pisi, Astrocystis bambusicola, Camposporium pellucidum, Dendryphiella phitsanulokensis, Diaporthe foeniculina, Didymella macrostoma, Diplodia mutila, Diplodia seriata, Heterosphaeria patella, Hysterobrevium constrictum, Neodidymelliopsis ranunculi, Neovaginatispora fuckelii, Nothophoma quercina, Occultibambusa bambusae, Phaeosphaeria chinensis, Pseudopestalotiopsis theae, Pyxine berteriana, Tetraploa sasicola, Torula gaodangensis and Wojnowiciella dactylidis. In addition, the sexual morphs of Dissoconium eucalypti and Phaeosphaeriopsis pseudoagavacearum are reported from Laurus nobilis and Yucca gloriosa in Italy, respectively. The holomorph of Diaporthe cynaroidis is also reported for the first time.

139 citations


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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
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 manuscript reviews fifty ways in which fungi can potentially be utilized as biotechnology and provides a flow chart that can be used to convince funding bodies of the importance of fungi for biotechnological research and as potential products.
Abstract: Fungi are an understudied, biotechnologically valuable group of organisms. Due to the immense range of habitats that fungi inhabit, and the consequent need to compete against a diverse array of other fungi, bacteria, and animals, fungi have developed numerous survival mechanisms. The unique attributes of fungi thus herald great promise for their application in biotechnology and industry. Moreover, fungi can be grown with relative ease, making production at scale viable. The search for fungal biodiversity, and the construction of a living fungi collection, both have incredible economic potential in locating organisms with novel industrial uses that will lead to novel products. This manuscript reviews fifty ways in which fungi can potentially be utilized as biotechnology. We provide notes and examples for each potential exploitation and give examples from our own work and the work of other notable researchers. We also provide a flow chart that can be used to convince funding bodies of the importance of fungi for biotechnological research and as potential products. Fungi have provided the world with penicillin, lovastatin, and other globally significant medicines, and they remain an untapped resource with enormous industrial potential.

404 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

Dissertation
01 Jan 2005
TL;DR: AM fungi suppress the development of B. sorokiniana in barley and should be considered for biocontrol of the disease causing organism, according to the data.
Abstract: The potential disease suppressiveness of arbuscular mycorrhizal (AM) fungi of various origins on Bipolaris sorokiniana in barley has been investigated. Firstly, a survey considering the occurrence of AM fungi in arable fields in Sweden were conducted with the aim to exploit site specific genetic resources in relation to disease suppressiveness. Arbuscular mycorrhizal fungi were present at all 45 sampling sites surveyed all over Sweden at densities ranging from 3 up to 44 spores per gram air dried soil. The highest spore density was found in a semi-natural grassland and the lowest were found in a cereal monoculture. The AM fungi were then multiplied in trap cultures in the greenhouse with the aim to use these for studying potential disease suppressiveness. Thus, the effects of the AM fungi trap cultures on the transmission of seed-borne B. sorokiniana in barley were investigated, using the trap culture inocula, but also including inocula consisting on spore mixtures. The arbuscular mycorrhizal fungi were able to suppress the transmission of B. sorokiniana in aerial parts of barley plants. The degree of suppression varied with the origin of the AM fungal trap cultures. The trap culture inoculum with the highest suppression of the B. sorokiniana transmission originated from an organically managed barley field with undersown ley. The two spore-inocula with the best suppression of the pathogen originated from fields with winter wheat and spring barley, respectively. Eventually, an in vitro method was developed for studying the effect of AM fungal colonisation of roots on the development of foliar diseases and the reaction of the actual host plant of the disease causing organism. Using the developed method, it was indicated that AM fungal colonisation of barley plant suppressed the development of leaf necroses due to B. sorokiniana. Further in vitro studies on the interaction between B. sorokiniana and arbuscular mycorrhizal fungi showed that B. sorokiniana decrease the germination of the AM fungal spores. In conclusion, AM fungi suppress the development of B. sorokiniana in barley. My data suggest that for biocontrol of B. sorokiniana AM fungi should be considered.

371 citations