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Amphisphaeria yunnanensis (HMAS 290476). a, b. Ascomata on the substrate. c. Vertical section of ascoma. d. Peridium. e. Paraphyses. f−i. Asci. j. J-Apical apparatus. k−m. Ascospores. n. Germinating ascospore. Culture on PDA from, o. above, p. below after 6 weeks. Scale bars: c = 100 μm, f−i = 20 μm, d,e, j−n = 5 μm.
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Amphisphaeria yunnanensis sp. nov. and Lepteutypa qujingensis sp. nov. are introduced in this study from dead twigs collected from an evergreen broadleaf forest area in Yunnan Province, China. Both species have immersed, sub-globose ascomata and overlapping uniseriate asci and multi-guttulate, fusiform, brown ascospores. Amphisphaeria yunnanensis i...
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Citations
... Rivera-Mariani et al. (2011 stated that in the Caribbean, ascospores produce greater sensitization than conidia in atopic individuals. On the other The genus Amphisphaeria has been studied taxonomically and phylogenetically (Dissanayake et al., 2020;Samarakoon et al., 2019Samarakoon et al., , 2020Senanayake et al., 2019). It is a saprobe ascomycete of decaying wood and is found in different habitats . ...
The airborne fungal spore content of the Havana city was studied from January to December 2017 by means a Hirst type volumetric methodology. Ten spore types were recorded for the first time in the atmosphere of the Cuba Island. A morphobiometrical description of the characteristics of each kind of spore was conducted. Four ascomycetes were identified (Amphisphaeria, Ascobolus, Cucurbidothis-type and Lewia) and six conidial genera were identified (Exosporium, Helicomina, Microsporum, Solheimia, and Trichocladium). Most of them are pantropical, saprophytes of different plants, and they could cause allergies or diseases in fruit crops of urban agriculture. This work increases the knowledge about the diversity of the airborne fungi in a neotropical region.
... DNA extraction, PCR amplification, sequencing, and phylogenetic analysis were done following the methods of Dissanayake et al. [58]. Mycelia for DNA extraction from each isolate was grown on PDA for 3-4 weeks at room temperature. ...
During the investigation of lignicolous freshwater fungi in plateau lakes in Yunnan Province, China, eight Lentitheciaceae species were collected from five lakes viz. Luguhu, Qiluhu, Xingyunhu, Cibihu, and Xihu lake. Based on morphological characters and phylogenetic analysis of combined ITS, LSU, SSU, and tef 1-α sequence data, a new genus Paralentithecium, two new species (Paralentithecium suae, and Setoseptoria suae), three new records (Halobyssothecium phragmitis, H. unicellulare, and Lentithecium yunnanensis) and three known species viz. Halobyssothecium aquifusiforme, Lentithecium pseudoclioninum, and Setoseptoria bambusae are reported.
... For phylogenetic inferences, two genetic markers, ITS and LSU, were applied ( Table 1). The phylogenetic tree was extrapolated using 58 taxa according to recent publications [21][22][23][24]. Maximum likelihood trees (ML) were constructed using IQ-Tree v.2 [25]. ...
... Most of the species of Amphisphaeria are found on grasses, woody branches, and some monocotyledons as saprobes in terrestrial habitats [30]. The unicellular ascospores of Amphisphaeria members typically have J+ or J− apical rings, solitary or aggregated ventral membranes under undeveloped perithecia or absent perithecia; and a coelomycetous asexual morphology with a light-to dark-brown color, oval to fusiform shape, and 1-3-noded ventral conidia [21][22][23][24]. The species of Amphisphaeria that have been reported are sexual morphs or coelomycetous asexual morphs, and no studies have reported hyphomycetous asexual morphs in this genus so far. ...
... lar ascospores of Amphisphaeria members typically have J+ or J− apical rings, solitary or aggregated ventral membranes under undeveloped perithecia or absent perithecia; and a coelomycetous asexual morphology with a light-to dark-brown color, oval to fusiform shape, and 1-3-noded ventral conidia [21][22][23][24]. The species of Amphisphaeria that have been reported are sexual morphs or coelomycetous asexual morphs, and no studies have reported hyphomycetous asexual morphs in this genus so far. ...
Endophytic fungi are a remarkably diverse group of microorganisms that have imperceptible associations with their hosts for at least a part of their life cycle. The enormous biological diversity and the capability of producing bioactive secondary metabolites such as alkaloids, terpenoids, and polyketides have attracted the attention of different scientific communities, resulting in numerous investigations on these fungal endophytes. During our surveys of plant-root-based fungi in the mountain areas of Qingzhen, Guizhou Province, several isolates of endophytic fungi were identified. In this study, a novel endophytic fungus was discovered in the roots of a medicinal plant (Orixa japonica) in Southern China and introduced as a new species (Amphisphaeria orixae) based on morphological evidence and molecular phylogenetic analysis (combined ITS and LSU sequence data). To the best of our knowledge, A. orixae is the first reported endophyte as well as the first hyphomycetous asexual morph in Amphisphaeria. A new isocoumarin, (R)-4,6,8-trihydroxy-5-methylisochroman-1-one (1), and 12 known compounds (2–13) were isolated from the rice fermentation products of this fungus. Using 1D- and 2D-NMR, mass spectrometry, and ECD studies, their structures were identified. The antitumor activity of these compounds was tested. Unfortunately, none of the compounds tested showed significant antitumor activity.
... Notes: Torulaceae comprises six genera Dendryphion, Neotorula, Rostriconidium, Rutola, Sporidesmioides and Torula (Crous et al. 2015b(Crous et al. , 2020aLi et al. 2016b;Su et al. 2016aSu et al. , 2018. Members of the family are only known in asexual morphs Li et al. 2020). ...
... Marincowitz et al. 2008;Liu et al. 2015a;Phookamsak et al. 2019;Samarakoon et al. 2019;Senanayake et al. 2019;Dissanayake et al. 2020).Samarakoon et al. (2020) reviewed the genus and ...
Freshwater fungi comprises a highly diverse group of organisms occurring in freshwater habitats throughout the world. During a survey of freshwater fungi on submerged wood in streams and lakes, a wide range of sexual and asexual species were collected mainly from karst regions in China and Thailand. Phylogenetic inferences using partial gene regions of LSU, ITS, SSU, TEF1α, and RPB2 sequences revealed that most of these fungi belonged to Dothideomycetes and Sordariomycetes and a few were related to Eurotiomycetes. Based on the morphology and multi-gene phylogeny, we introduce four new genera, viz. Aquabispora, Neocirrenalia, Ocellisimilis and Uvarisporella, and 47 new species, viz. Acrodictys chishuiensis, A. effusa, A. pyriformis, Actinocladium aquaticum, Annulatascus tratensis, Aquabispora setosa, Aqualignicola setosa, Aquimassariosphaeria vermiformis, Ceratosphaeria flava, Chaetosphaeria polygonalis, Conlarium muriforme, Digitodesmium chishuiense, Ellisembia aquirostrata, Fuscosporella atrobrunnea, Halobyssothecium aquifusiforme, H. caohaiense, Hongkongmyces aquisetosus, Kirschsteiniothelia dushanensis, Monilochaetes alsophilae, Mycoenterolobium macrosporum, Myrmecridium splendidum, Neohelicascus griseoflavus, Neohelicomyces denticulatus, Neohelicosporium fluviatile, Neokalmusia aquibrunnea, Neomassariosphaeria aquimucosa, Neomyrmecridium naviculare, Neospadicoides biseptata, Ocellisimilis clavata, Ophioceras thailandense, Paragaeumannomyces aquaticus, Phialoturbella aquilunata, Pleurohelicosporium hyalinum, Pseudodactylaria denticulata, P. longidenticulata, P. uniseptata, Pseudohalonectria aurantiaca, Rhamphoriopsis aquimicrospora, Setoseptoria bambusae, Shrungabeeja fluviatilis, Sporidesmium tratense, S. versicolor, Sporoschisma atroviride, Stanjehughesia aquatica, Thysanorea amniculi, Uvarisporella aquatica and Xylolentia aseptata, with an illustrated account, discussion of their taxonomic placement and comparison with morphological similar taxa. Seven new combinations are introduced, viz. Aquabispora grandispora (≡ Boerlagiomyces grandisporus), A. websteri (≡ Boerlagiomyces websteri), Ceratosphaeria suthepensis (≡ Pseudohalonectria suthepensis), Gamsomyces aquaticus (≡ Pseudobactrodesmium aquaticum), G. malabaricus (≡ Gangliostilbe malabarica), Neocirrenalia nigrospora (≡ Cirrenalia nigrospora), and Rhamphoriopsis glauca (≡ Chloridium glaucum). Ten new geographical records are reported in China and Thailand and nine species are first reported from freshwater habitats. Reference specimens are provided for Diplocladiella scalaroides and Neocirrenalia nigrospora (≡ Cirrenalia nigrospora). Systematic placement of the previously introduced genera Actinocladium, Aqualignicola, and Diplocladiella is first elucidated based on the reference specimens and new collections. Species recollected from China and Thailand are also described and illustrated. The overall trees of freshwater Dothideomycetes and Sordariomycetes collected in this study are provided respectively and genera or family/order trees are constructed for selected taxa.
As the continuation of Fungal Diversity Notes series, the current paper is the 16th contribution to this series. A total of 103 taxa from seven classes in Ascomycota and Basidiomycota are included here. Of these 101 taxa, four new genera, 89 new species, one new combination, one new name and six new records are described in detail along with information of hosts and geographic distributions. The four genera newly introduced are Ascoglobospora, Atheliella, Rufoboletus and Tenuimyces. Newly described species are Akanthomyces xixiuensis, Agaricus agharkarii, A. albostipitatus, Amphisphaeria guttulata, Ascoglobospora marina, Astrothelium peudostraminicolor, Athelia naviculispora, Atheliella conifericola, Athelopsis subglaucina, Aureoboletus minimus, A. nanlingensis, Autophagomyces incertus, Beltrania liliiferae, Beltraniella jiangxiensis, Botryobasidium coniferarum, Calocybella sribuabanensis, Calonarius caesiofulvus, C. nobilis, C. pacificus, C. pulcher, C. subcorrosus, Cortinarius flaureifolius, C. floridaensis, C. subiodes, Crustomyces juniperi, C. scytinostromoides, Cystostereum subsirmaurense, Dimorphomyces seemanii, Fulvoderma microporum, Ginnsia laricicola, Gomphus zamorinorum, Halobyssothecium sichuanense, Hemileccinum duriusculum, Henningsomyces hengduanensis, Hygronarius californicus, Kneiffiella pseudoabdita, K. pseudoalutacea, Laboulbenia bifida, L. tschirnhausii, L. tuberculata, Lambertella dipterocarpacearum, Laxitextum subrubrum, Lyomyces austro-occidentalis, L. crystallina, L. guttulatus, L. niveus, L. tasmanicus, Marasmius centrocinnamomeus, M. ferrugineodiscus, Megasporoporia tamilnaduensis, Meruliopsis crystallina, Metuloidea imbricata, Moniliophthora atlantica, Mystinarius ochrobrunneus, Neomycoleptodiscus alishanense, Nigrograna kunmingensis, Paracremonium aquaticum, Parahelicomyces dictyosporus, Peniophorella sidera, P. subreticulata, Phlegmacium fennicum, P. pallidocaeruleum, Pholiota betulicola, P. subcaespitosa, Pleurotheciella hyalospora, Pleurothecium aseptatum, Resupinatus porrigens, Russula chlorina, R. chrysea, R. cruenta, R. haematina, R. luteocarpa, R. sanguinolenta, Synnemellisia punensis, Tenuimyces bambusicola, Thaxterogaster americanoporphyropus, T. obscurovibratilis, Thermoascus endophyticus, Trechispora alba, T. perminispora, T. subfarinacea, T. tuberculata, Tremella sairandhriana, Tropicoporus natarajaniae, T. subramaniae, Usnea kriegeriana, Wolfiporiella macrospora and Xylodon muchuanensis. Rufoboletus hainanensis is newly transferred from Butyriboletus, while a new name Russula albocarpa is proposed for Russula leucocarpa G.J. Li & Chun Y. Deng an illegitimate later homonym of Russula leucocarpa (T. Lebel) T. Lebel. The new geographic distribution regions are recorded for Agaricus bambusetorum, Bipolaris heliconiae, Crinipellis trichialis, Leucocoprinus cretaceus, Halobyssothecium cangshanense and Parasola setulosa. Corresponding to morphological characters, phylogenetic evidence is also utilized to place the above-mentioned taxa in appropriate taxonomic positions. The current morphological and phylogenetic data is helpful for further clarification of species diversity and exploration of evolutionary relationships in the related fungal groups.
During the continuous investigation into inconspicuous xylarialean
species in northern Thailand, two amphisphaeria-like taxa were
found in samples collected between July and October 2022. Both
taxa have solitary, immersed ascomata with a two-layered
peridium and unitunicate asci that are morphologically similar to
Amphisphaeria species. Macro–micro morphological comparisons
with related taxa and multigene phylogenetic analyses based on
combined internal transcribed spacer (ITS), partial 28S large
subunit rDNA (LSU), partial RNA polymerase II second largest
subunit (rpb2), and partial β-tubulin (tub2) sequences revealed
that the two taxa are novel to science. Amphisphaeria
chiangmaiensis sp. nov. is distinguished from known taxa by
having larger ascomata, a J- apical ring in Melzer’s reagent, and
hyaline ascospores. Amphisphaeria hydei sp. nov. differs from its
sister taxa in having larger ascomata, a longer ostiolar canal, and
longer asci. Morphological descriptions, illustrations, and
phylogenetic analyses of two novel taxa are provided herein.
This study documents the morphology and phylogeny of ascomycetes collected from karst landscapes of Guizhou Province, China. Based on morphological characteristics in conjunction with DNA sequence data, 70 species are identified and distributed in two classes (Dothideomycetes and Sordariomycetes), 16 orders, 41 families and 60 genera. One order Planisphaeriales, four families Leptosphaerioidaceae, Neoleptosporellaceae, Planisphaeriaceae and Profundisphaeriaceae, ten genera Conicosphaeria, Karstiomyces, Leptosphaerioides, Neoceratosphaeria, Neodiaporthe, Neodictyospora, Planisphaeria, Profundisphaeria, Stellatus and Truncatascus, and 34 species (Amphisphaeria karsti, Anteaglonium hydei, Atractospora terrestris, Conicosphaeria vaginatispora, Corylicola hydei, Diaporthe cylindriformispora, Dictyosporium karsti, Hysterobrevium karsti, Karstiomyces guizhouensis, Leptosphaerioides guizhouensis, Lophiotrema karsti, Murispora hydei, Muyocopron karsti, Neoaquastroma guizhouense, Neoceratosphaeria karsti, Neodiaporthe reniformispora, Neodictyospora karsti, Neoheleiosa guizhouensis, Neoleptosporella fusiformispora, Neoophiobolus filiformisporum, Ophioceras guizhouensis, Ophiosphaerella karsti, Paraeutypella longiasca, Paraeutypella karsti, Patellaria guizhouensis, Planisphaeria karsti, Planisphaeria reniformispora, Poaceascoma herbaceum, Profundisphaeria fusiformispora, Pseudocoleophoma guizhouensis, Pseudopolyplosphaeria guizhouensis, Stellatus guizhouensis, Sulcatispora karsti and Truncatascus microsporus) are introduced as new to science. Moreover, 13 new geographical records for China are also reported, which are Acrocalymma medicaginis, Annulohypoxylon thailandicum, Astrosphaeriella bambusae, Diaporthe novem, Hypoxylon rubiginosum, Ophiosphaerella agrostidis, Ophiosphaerella chiangraiensis, Patellaria atrata, Polyplosphaeria fusca, Psiloglonium macrosporum, Sarimanas shirakamiense, Thyridaria broussonetiae and Tremateia chromolaenae. Additionally, the family Eriomycetaceae was resurrected as a non-lichenized family and accommodated within Monoblastiales. Detailed descriptions and illustrations of all these taxa are provided.
During our investigation of ascomycetes fungi on Poaceae, a microdochium-like fungus was collected from dead grass leaves from a terrestrial habitat in Chengdu, Sichuan Province, China. Based on morphological characterization and phylogenetic analyses, we introduce this fungus as Microdochium sichuanense sp. nov. Maximum likelihood, and Bayesian analyses of combined genes (LSU, ITS and rpb2) were performed to clarify the phylogenetic affinities of the new species. Microdochium sichuanense is phylogenetically closely related to M. hainanense and morphologically it fits the generic characteristics of Microdochium species in having ostiolate ascomata, peridium cells of textura angularis to textura prismatica, unitunicate, clavate to oblong, 8-spored asci and hyaline, oval to fusiform ascospores. The new species was compared with phylogenetically and morphologically closely related species, and detailed descriptions, micrographs, and phylogenetic trees of the new species are provided.
Co-evolutionary relationships of plants and fungi are of great importance for the phylogeny of both groups. Nyssa was widely distributed in the northern hemisphere during the Cenozoic. Extant species of Nyssa exhibit a disjunct distribution between eastern North America, Central America and East Asia. Here, a new species, Nyssa nanningensis Xu & Jin, is described based on fruit endocarps from the upper Oligocene Yongning Formation of the Nanning Basin, South China. This new fossil record of Nyssa expands the known palaeogeographical distribution of the genus to the low latitudes of East Asia. Associated fossil fungal fruiting bodies on Nyssa endocarps are assigned to the new fossil genus and species, Yongnicta nyssae Tobias & Maslova. This new genus is similar to some members of extant wood destructor taxa Coronophorales and Amphisphaeriales (Sordariomycetes, Ascomycota). About 3% of the Nyssa endocarps studied were affected by Yongnicta nyssae. Low frequency of fruit damage indicates that endocarps could be released from mesocarps by animals eating fleshy parts of fruits, making them potentially available to wood-destroying fungi.
Amphisphaeriaceous taxa (fungi) are saprobes on decaying wood in terrestrial, mangrove, and freshwater habitats. The generic boundaries of the family have traditionally been based on morphology, and the delimitation of genera has always been challenging. Amphisphaeria species have clypeate ascomata and 1-septate ascospores and a coelomycetous asexual morph. Lepteutypa is different from Amphisphaeria in having eutypoid stromata and more than 1-septate ascospores. These main characters have been used for segregation of Lepteutypa from Amphisphaeria for a long time. However, the above characters are overlapping among Amphisphaeria and Lepteutypa species. Therefore, here we synonymized Lepteutypa under Amphisphaeria based on holomorphic morphology and multigene phylogeny. Further, our cluster analysis reveals the relationship between seven morphological traits among Amphisphaeria/Lepteutypa species and suggests those morphologies are not specific to either genus. Three new species (i.e., Amphisphaeria camelliae, A. curvaticonidia, and A. micheliae) are introduced based on morphology and LSU-ITS-RPB2-TUB2 phylogenies. Furthermore, the monotypic genus Trochilispora, which had been accepted in Amphisphaeriaceae, is revisited and synonymized under Hymenopleella and placed in Sporocadaceae.
