One stop shop V: taxonomic update with molecular phylogeny for important phytopathogenic genera: 101–125 (2024) DOI
Ruvishika S. Jayawardena, Kevin D. Hyde, Herbert Dustin Aumentado

и другие.

Fungal Diversity, Год журнала: 2025, Номер unknown

Опубликована: Фев. 18, 2025

Язык: Английский

Notes, outline and divergence times of Basidiomycota DOI Creative Commons

Mao-Qiang He,

Rui-Lin Zhao, Kevin D. Hyde

и другие.

Fungal Diversity, Год журнала: 2019, Номер 99(1), С. 105 - 367

Опубликована: Ноя. 1, 2019

Abstract The Basidiomycota constitutes a major phylum of the kingdom Fungi and is second in species numbers to Ascomycota. present work provides an overview all validly published, currently used basidiomycete genera date single document. An outline provided, which includes 1928 names, with 1263 synonyms, are distributed 241 families, 68 orders, 18 classes four subphyla. We provide brief notes for each accepted genus including information on classification, number species, type life mode, habitat, distribution, sequence information. Furthermore, three phylogenetic analyses combined LSU, SSU, 5.8s, rpb1, rpb2, ef1 datasets subphyla Agaricomycotina, Pucciniomycotina Ustilaginomycotina conducted, respectively. Divergence time estimates provided family level 632 from 62 168 families 605 genera. Our study indicates that divergence times 406–430 Mya, 211–383 orders 99–323 largely consistent previous studies. In this study, phylogenetically supported were dated, Agaricomycotina diverging 27–178 85–222 79–177 Mya. as additional criterion ranking evidence resolve taxonomic problems system, also better understanding their phylogeny evolution.

Язык: Английский

Процитировано

408

Fungal diversity notes 929–1035: taxonomic and phylogenetic contributions on genera and species of fungi DOI Creative Commons
Rungtiwa Phookamsak, Kevin D. Hyde, Rajesh Jeewon

и другие.

Fungal Diversity, Год журнала: 2019, Номер 95(1), С. 1 - 273

Опубликована: Март 1, 2019

This article is the ninth in series of Fungal Diversity Notes, where 107 taxa distributed three phyla, nine classes, 31 orders and 57 families are described illustrated. Taxa present study include 12 new genera, 74 species, combinations, two reference specimens, a re-circumscription epitype, 15 records sexual-asexual morph connections, hosts geographical distributions. Twelve genera comprise Brunneofusispora, Brunneomurispora, Liua, Lonicericola, Neoeutypella, Paratrimmatostroma, Parazalerion, Proliferophorum, Pseudoastrosphaeriellopsis, Septomelanconiella, Velebitea Vicosamyces. Seventy-four species Agaricus memnonius, A. langensis, Aleurodiscus patagonicus, Amanita flavoalba, 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 Neobambusicola brunnea, Neoeutypella Neoroussoella heveae, Neosetophoma Ophiobolus malleolus, Parabambusicola Paratrimmatostroma Parazalerion Penicillium dokdoense, Peroneutypa Phaeosphaeria cycadis, Phanerochaete australosanguinea, Plectosphaerella Plenodomus artemisiae, P. lijiangensis, Proliferophorum thailandicum, Pseudoastrosphaeriellopsis kaveriana, Pseudohelicomyces menglunicus, Pseudoplagiostoma mangiferae, Robillarda Roussoella elaeicola, Russula choptae, R. uttarakhandia, Septomelanconiella thailandica, Spencermartinsia acericola, Sphaerellopsis isthmospora, Thozetella lithocarpi, Trechispora echinospora, Tremellochaete atlantica, Trichoderma koreanum, T. pinicola, rugulosum, chrysotexta, Vicosamyces venturisporus, Wojnowiciella kunmingensis Zopfiella indica. Three combinations rufomaculata, Lanmaoa pallidorosea rosicola. The specimens Canalisporium kenyense Tamsiniella labiosa designated. epitype Sarcopeziza sicula re-circumscribed based on cyto- histochemical analyses. connection sinensis reported from ferns Cirsium for first time. In addition, host country altipes, melleialba, Amarenomyces dactylidis, Chaetosphaeria panamensis, Coniella vitis, Coprinopsis kubickae, Dothiorella sarmentorum, Leptobacillium leptobactrum var. calidus, Muyocopron solani, Periconia cortaderiae, Phragmocamarosporium hederae, paraphysata Sphaeropsis eucalypticola.

Язык: Английский

Процитировано

292

Fungal diversity notes 1151–1276: taxonomic and phylogenetic contributions on genera and species of fungal taxa DOI Creative Commons
Kevin D. Hyde, Yang Dong, Rungtiwa Phookamsak

и другие.

Fungal Diversity, Год журнала: 2020, Номер 100(1), С. 5 - 277

Опубликована: Янв. 1, 2020

Abstract Fungal diversity notes is one of the important journal series fungal taxonomy that provide detailed descriptions and illustrations new taxa, as well providing information taxa worldwide. This article 11th contribution to series, in which 126 distributed two phyla, six classes, 24 orders 55 families are described illustrated. Taxa this study were mainly collected from Italy by Erio Camporesi also China, India Thailand, some other European, North American South countries. present include families, 12 genera, 82 species, five combinations 25 records on hosts geographical distributions sexual-asexual reports. The Eriomycetaceae (Dothideomycetes, family incertae sedis ) Fasciatisporaceae ( Xylariales , Sordariomycetes). twelve genera comprise Bhagirathimyces Phaeosphaeriaceae ), Camporesiomyces Tubeufiaceae Eriocamporesia Cryphonectriaceae Eriomyces Neomonodictys Pleurotheciaceae Paraloratospora Paramonodictys Parabambusicolaceae Pseudoconlarium (Diaporthomycetidae, genus Pseudomurilentithecium Lentitheciaceae Setoapiospora Muyocopronaceae Srinivasanomyces Vibrisseaceae Xenoanthostomella ). species Acremonium chiangraiense Adustochaete nivea Angustimassarina camporesii himalayensis Brunneoclavispora Camarosporidiella mali Camposporium appendiculatum multiseptatum septatum Canalisporium aquaticium Clonostachys eriocamporesiana eriocamporesii Colletotrichum hederiicola Coniochaeta vineae Conioscypha verrucosa Cortinarius ainsworthii aurae britannicus heatherae scoticus subsaniosus Cytospora fusispora rosigena Diaporthe nigra Diatrypella yunnanensis Dictyosporium muriformis Didymella Diutina bernali sipiczkii aurantia heveae Ernakulamia tanakae Falciformispora uttaraditensis Fasciatispora cocoes Foliophoma Fuscostagonospora Helvella subtinta Kalmusia erioi Keissleriella camporesiana Lanspora cylindrospora Loratospora arezzoensis Mariannaea atlantica Melanographium phoenicis Montagnula Neodidymelliopsis Neokalmusia kunmingensis Neoleptosporella Neomyrmecridium guizhouense Neosetophoma solitarius Periconia palmicola Plenodomus triseptatus Pseudocamarosporium Pseudocercospora maetaengensis Pseudochaetosphaeronema kunmingense punctiforme Pseudodactylaria Pseudotetraploa rajmachiensis Pseudotruncatella Rhexocercosporidium senecionis Rhytidhysteron Septoriella thailandica kangrensis Tetraploa dwibahubeeja pseudoaristata thrayabahubeeja Torula Tremateia lamiacearum Uzbekistanica pruni Verruconis mangrovei Wilcoxina verruculosa chromolaenae Xenodidymella . patagoniensis vaccinia lycopodiellae gahniae microsporum 22 host distribution Arthrinium marii Ascochyta medicaginicola pisi Astrocystis bambusicola pellucidum Dendryphiella phitsanulokensis foeniculina macrostoma Diplodia mutila seriata Heterosphaeria patella Hysterobrevium constrictum ranunculi Neovaginatispora fuckelii Nothophoma quercina Occultibambusa bambusae Phaeosphaeria chinensis Pseudopestalotiopsis theae Pyxine berteriana sasicola gaodangensis Wojnowiciella dactylidis In addition, sexual morphs Dissoconium eucalypti Phaeosphaeriopsis pseudoagavacearum reported Laurus nobilis Yucca gloriosa Italy, respectively. holomorph cynaroidis for first time.

Язык: Английский

Процитировано

219

Colletotrichum species and complexes: geographic distribution, host range and conservation status DOI
Pedro Talhinhas, Riccardo Baroncelli

Fungal Diversity, Год журнала: 2021, Номер 110(1), С. 109 - 198

Опубликована: Сен. 1, 2021

Язык: Английский

Процитировано

209

The numbers of fungi: is the descriptive curve flattening? DOI
Kevin D. Hyde, Rajesh Jeewon,

Yi-Jyun Chen

и другие.

Fungal Diversity, Год журнала: 2020, Номер 103(1), С. 219 - 271

Опубликована: Июль 1, 2020

Язык: Английский

Процитировано

185

Integrative approaches for species delimitation in Ascomycota DOI
Sajeewa S. N. Maharachchikumbura, Yanpeng Chen, Hiran A. Ariyawansa

и другие.

Fungal Diversity, Год журнала: 2021, Номер 109(1), С. 155 - 179

Опубликована: Июль 1, 2021

Язык: Английский

Процитировано

133

The numbers of fungi: are the most speciose genera truly diverse? DOI
Chitrabhanu S. Bhunjun, Tuula Niskanen, Nakarin Suwannarach

и другие.

Fungal Diversity, Год журнала: 2022, Номер 114(1), С. 387 - 462

Опубликована: Март 27, 2022

Язык: Английский

Процитировано

125

Investigating species boundaries in Colletotrichum DOI
Chitrabhanu S. Bhunjun, Chayanard Phukhamsakda, Ruvishika S. Jayawardena

и другие.

Fungal Diversity, Год журнала: 2021, Номер 107(1), С. 107 - 127

Опубликована: Март 1, 2021

Язык: Английский

Процитировано

117

Fungal diversity notes 1512–1610: taxonomic and phylogenetic contributions on genera and species of fungal taxa DOI Open Access
Ruvishika S. Jayawardena,

K. D. Hyde,

Song Wang

и другие.

Fungal Diversity, Год журнала: 2022, Номер 117(1), С. 1 - 272

Опубликована: Ноя. 1, 2022

Язык: Английский

Процитировано

96

Significance of precise documentation of hosts and geospatial data of fungal collections, with an emphasis on plant-associated fungi DOI
Achala R. Rathnayaka, Danushka S. Tennakoon, E.B. Gareth Jones

и другие.

New Zealand Journal of Botany, Год журнала: 2024, Номер unknown, С. 1 - 28

Опубликована: Июль 28, 2024

In taxonomy, precision of species collection data is a cornerstone for advancing research and its diverse applications. Despite the widespread recognition significance these data, researchers have frequently neglected some important details in published taxonomic studies. Historically, fungal studies leaned heavily on morphological delineation taxa. contrast, methods currently employ synthesis combination morpho-molecular markers, chemical attributes both ecological geographic data. Even with new methods, mycologists value derived from old records as essential guides current future Therefore, this underscores importance careful documentation habits habitats parallel collection. While collecting specimens fungi, it to record metadata such sampling location, habitat (host/substrate), season (date or specific season) physical information specimen itself. These datasets will provide rich source ecology conservation resources. Understanding distribution patterns possible explanations real challenge conserving biodiversity, lack data-recording creates substantial obstacles. Accurate fungarium are basic understanding richness assessing red-listed invasive species. This paper explores additions recording, emphasising hosts locations. We also discuss significant roles seemingly insignificant recording enhance about relationships

Язык: Английский

Процитировано

39