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Papulosaceae, Sordariomycetes, Ascomycota) Hyphopodiate Fungus with a Phialophora Anamorph from Grass Inferred from Morphological and Molecular Data
IMA FUNGUS · 7(2): 247–252 (2016) doi:10.5598/imafungus.2016.07.02.04 Wongia gen. nov. (Papulosaceae, Sordariomycetes), a new generic name ARTICLE for two root-infecting fungi from Australia Wanporn Khemmuk1,2, Andrew D.W. Geering1,2, and Roger G. Shivas2,3 1Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, Ecosciences Precinct, GPO Box 267, Brisbane, Queensland, 4001, Australia 2Plant Biosecurity Cooperative Research Centre, LPO Box 5012, Bruce, ACT 2617, Australia 3Plant Pathology Herbarium, Department of Agriculture and Fisheries, Ecosciences Precinct, Dutton Park 4102, Australia; corresponding author e-mail: [email protected] Abstract: The classification of two root-infecting fungi, Magnaporthe garrettii and M. griffinii, was examined Key words: by phylogenetic analysis of multiple gene sequences. This analysis demonstrated that M. garrettii and M. Ascomycota griffinii were sister species that formed a well-supported separate clade in Papulosaceae (Diaporthomycetidae, Cynodon Sordariomycetes), which clusters outside of the Magnaporthales. Wongia gen. nov, is established to Diaporthomycetidae accommodate these two species which are not closely related to other species classified in Magnaporthe nor multigene analysis to other genera, including Nakataea, Magnaporthiopsis and Pyricularia, which all now contain other species one fungus-one name once classified in Magnaporthe. molecular phylogenetics root pathogens Article info: Submitted: 5 July 2016; Accepted: 7 October 2016; Published: 11 October 2016. INTRODUCTION species, M. griffinii, was found by Klaubauf et al. (2014) to be distant from Sordariomycetes based on ITS sequences The taxonomic and nomenclatural problems that surround (GenBank JQ390311, JQ390312). generic names in the Magnaporthales (Sordariomycetes, This study aims to resolve the classification ofM. -
Co-Adaptations Between Ceratocystidaceae Ambrosia Fungi and the Mycangia of Their Associated Ambrosia Beetles
Iowa State University Capstones, Theses and Graduate Theses and Dissertations Dissertations 2018 Co-adaptations between Ceratocystidaceae ambrosia fungi and the mycangia of their associated ambrosia beetles Chase Gabriel Mayers Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/etd Part of the Biodiversity Commons, Biology Commons, Developmental Biology Commons, and the Evolution Commons Recommended Citation Mayers, Chase Gabriel, "Co-adaptations between Ceratocystidaceae ambrosia fungi and the mycangia of their associated ambrosia beetles" (2018). Graduate Theses and Dissertations. 16731. https://lib.dr.iastate.edu/etd/16731 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Graduate Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Co-adaptations between Ceratocystidaceae ambrosia fungi and the mycangia of their associated ambrosia beetles by Chase Gabriel Mayers A dissertation submitted to the graduate faculty in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Major: Microbiology Program of Study Committee: Thomas C. Harrington, Major Professor Mark L. Gleason Larry J. Halverson Dennis V. Lavrov John D. Nason The student author, whose presentation of the scholarship herein was approved by the program of study committee, is solely responsible for the content of this dissertation. The Graduate College will ensure this dissertation is globally accessible and will not permit alterations after a degree is conferred. Iowa State University Ames, Iowa 2018 Copyright © Chase Gabriel Mayers, 2018. -
Discovery of the Teleomorph of the Hyphomycete, Sterigmatobotrys Macrocarpa, and Epitypification of the Genus to Holomorphic Status
available online at www.studiesinmycology.org StudieS in Mycology 68: 193–202. 2011. doi:10.3114/sim.2011.68.08 Discovery of the teleomorph of the hyphomycete, Sterigmatobotrys macrocarpa, and epitypification of the genus to holomorphic status M. Réblová1* and K.A. Seifert2 1Department of Taxonomy, Institute of Botany of the Academy of Sciences, CZ – 252 43, Průhonice, Czech Republic; 2Biodiversity (Mycology and Botany), Agriculture and Agri- Food Canada, Ottawa, Ontario, K1A 0C6, Canada *Correspondence: Martina Réblová, [email protected] Abstract: Sterigmatobotrys macrocarpa is a conspicuous, lignicolous, dematiaceous hyphomycete with macronematous, penicillate conidiophores with branches or metulae arising from the apex of the stipe, terminating with cylindrical, elongated conidiogenous cells producing conidia in a holoblastic manner. The discovery of its teleomorph is documented here based on perithecial ascomata associated with fertile conidiophores of S. macrocarpa on a specimen collected in the Czech Republic; an identical anamorph developed from ascospores isolated in axenic culture. The teleomorph is morphologically similar to species of the genera Carpoligna and Chaetosphaeria, especially in its nonstromatic perithecia, hyaline, cylindrical to fusiform ascospores, unitunicate asci with a distinct apical annulus, and tapering paraphyses. Identical perithecia were later observed on a herbarium specimen of S. macrocarpa originating in New Zealand. Sterigmatobotrys includes two species, S. macrocarpa, a taxonomic synonym of the type species, S. elata, and S. uniseptata. Because no teleomorph was described in the protologue of Sterigmatobotrys, we apply Article 59.7 of the International Code of Botanical Nomenclature. We epitypify (teleotypify) both Sterigmatobotrys elata and S. macrocarpa to give the genus holomorphic status, and the name S. -
Composition and Diversity of Fungal Decomposers of Submerged Wood in Two Lakes in the Brazilian Amazon State of Para´
Hindawi International Journal of Microbiology Volume 2020, Article ID 6582514, 9 pages https://doi.org/10.1155/2020/6582514 Research Article Composition and Diversity of Fungal Decomposers of Submerged Wood in Two Lakes in the Brazilian Amazon State of Para´ Eveleise SamiraMartins Canto ,1,2 Ana Clau´ dia AlvesCortez,3 JosianeSantana Monteiro,4 Flavia Rodrigues Barbosa,5 Steven Zelski ,6 and João Vicente Braga de Souza3 1Programa de Po´s-Graduação da Rede de Biodiversidade e Biotecnologia da Amazoˆnia Legal-Bionorte, Manaus, Amazonas, Brazil 2Universidade Federal do Oeste do Para´, UFOPA, Santare´m, Para´, Brazil 3Instituto Nacional de Pesquisas da Amazoˆnia, INPA, Laborato´rio de Micologia, Manaus, Amazonas, Brazil 4Museu Paraense Emilio Goeldi-MPEG, Bele´m, Para´, Brazil 5Universidade Federal de Mato Grosso, UFMT, Sinop, Mato Grosso, Brazil 6Miami University, Department of Biological Sciences, Middletown, OH, USA Correspondence should be addressed to Eveleise Samira Martins Canto; [email protected] and Steven Zelski; [email protected] Received 25 August 2019; Revised 20 February 2020; Accepted 4 March 2020; Published 9 April 2020 Academic Editor: Giuseppe Comi Copyright © 2020 Eveleise Samira Martins Canto et al. *is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Aquatic ecosystems in tropical forests have a high diversity of microorganisms, including fungi, which -
Morpho-Molecular Characterization and Epitypification of Annulatascus Velatisporus Article
Mycosphere 7 (9): 1389–1398 (2016) www.mycosphere.org ISSN 2077 7019 Article – special issue Doi 10.5943/mycosphere/7/9/12 Copyright © Guizhou Academy of Agricultural Sciences Morpho-molecular characterization and epitypification of Annulatascus velatisporus Dayarathne MC1,2,3,4, Maharachchikumbura SSN5, Phookamsak R1,2,3, Fryar SC6, To-anun C4, Jones EBG4, Al-Sadi AM5, Zelski SE7 and Hyde KD1,2,3* 1 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand. 2 World Agro forestry Centre East and Central Asia Office, 132 Lanhei Road, Kunming 650201, China. 3 Key Laboratory for Plant Biodiversity and Biogeography of East Asia (KLPB), Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan China. 4 Division of Plant Pathology, Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai 50200, Thailand. 5 Department of Crop Sciences, College of Agricultural and Marine Sciences, Sultan Qaboos University, PO Box 34, 123 Al Khoud, Oman. 6 Flinders University, School of Biology, GPO Box 2100, Adelaide SA 5001, Australia. 7 Department of Plant Biology, University of Illinois at Urbana-Champaign, Room 265 Morrill Hall, 505 South Goodwin Avenue, Urbana, IL 61801. Dayarathne MC, Maharachchikumbura SSN, Phookamsak R, Fryar SC, To-anun C, Jones EBG, Al- Sadi AM, Zelski SE, Hyde KD 2016 – Morpho-molecular characterization and epitypification of Annulatascus velatisporus. Mycosphere 7 (9), 1389–1398, Doi 10.5943/mycosphere/7/9/12 Abstract The holotype of Annulatascus velatisporus, the type species of the genus Annulatascus, which is the core species of Annulatascaceae (Annulatascales) is in poor condition as herbarium material has few ascomata and molecular data could not be generated. -
Multigene Phylogeny and Secondary ITS Structure
Persoonia 35, 2015: 21–38 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158515X687434 Molecular systematics of Barbatosphaeria (Sordariomycetes): multigene phylogeny and secondary ITS structure M. Réblová1, K. Réblová2, V. Štěpánek3 Key words Abstract Thirteen morphologically similar strains of barbatosphaeria- and tectonidula-like fungi were studied based on the comparison of cultural and morphological features of sexual and asexual morphs and phylogenetic analyses phylogenetics of five nuclear loci, i.e. internal transcribed spacer rDNA operon (ITS), large and small subunit nuclear ribosomal Ramichloridium DNA, β-tubulin, and second largest subunit of RNA polymerase II. Phylogenetic results were supported by in-depth sequence analysis comparative analyses of common core secondary structure of ITS1 and ITS2 in all strains and the identification spacer regions of non-conserved, co-evolving nucleotides that maintain base pairing in the RNA transcript. Barbatosphaeria is Sporothrix defined as a well-supported monophyletic clade comprising several lineages and is placed in the Sordariomycetes Tectonidula incertae sedis. The genus is expanded to encompass nine species with both septate and non-septate ascospores in clavate, stipitate asci with a non-amyloid apical annulus and non-stromatic ascomata with a long decumbent neck and carbonised wall often covered by pubescence. The asexual morphs are dematiaceous hyphomycetes with holoblastic conidiogenesis belonging to Ramichloridium and Sporothrix types. The morphologically similar Tectonidula, represented by the type species T. hippocrepida, grouped with members of Barbatosphaeria and is transferred to that genus. Four new species are introduced and three new combinations in Barbatosphaeria are proposed. A dichotomous key to species accepted in the genus is provided. -
Savoryellales (Hypocreomycetidae, Sordariomycetes): a Novel Lineage
Mycologia, 103(6), 2011, pp. 1351–1371. DOI: 10.3852/11-102 # 2011 by The Mycological Society of America, Lawrence, KS 66044-8897 Savoryellales (Hypocreomycetidae, Sordariomycetes): a novel lineage of aquatic ascomycetes inferred from multiple-gene phylogenies of the genera Ascotaiwania, Ascothailandia, and Savoryella Nattawut Boonyuen1 Canalisporium) formed a new lineage that has Mycology Laboratory (BMYC), Bioresources Technology invaded both marine and freshwater habitats, indi- Unit (BTU), National Center for Genetic Engineering cating that these genera share a common ancestor and Biotechnology (BIOTEC), 113 Thailand Science and are closely related. Because they show no clear Park, Phaholyothin Road, Khlong 1, Khlong Luang, Pathumthani 12120, Thailand, and Department of relationship with any named order we erect a new Plant Pathology, Faculty of Agriculture, Kasetsart order Savoryellales in the subclass Hypocreomyceti- University, 50 Phaholyothin Road, Chatuchak, dae, Sordariomycetes. The genera Savoryella and Bangkok 10900, Thailand Ascothailandia are monophyletic, while the position Charuwan Chuaseeharonnachai of Ascotaiwania is unresolved. All three genera are Satinee Suetrong phylogenetically related and form a distinct clade Veera Sri-indrasutdhi similar to the unclassified group of marine ascomy- Somsak Sivichai cetes comprising the genera Swampomyces, Torpedos- E.B. Gareth Jones pora and Juncigera (TBM clade: Torpedospora/Bertia/ Mycology Laboratory (BMYC), Bioresources Technology Melanospora) in the Hypocreomycetidae incertae -
Freshwater Fungi from the River Nile, Egypt
Mycosphere 7 (5): 741–756 (2016) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/7/6/4 Copyright © Guizhou Academy of Agricultural Sciences Freshwater fungi from the River Nile, Egypt Abdel-Aziz FA Department of Botany and Microbiology, Faculty of Science, Sohag University, Sohag 82524, Egypt Abdel-Aziz FA 2016 – Freshwater fungi from the River Nile, Egypt. Mycosphere 7(6), 741–756, Doi 10.5943/mycosphere/7/6/4 Abstract This study represents the first published data of freshwater fungi from the River Nile in Egypt. Knowledge concerning the geographic distribution of freshwater ascomycetes and their asexual morphs in Egypt and in the Middle East is limited. Ninety-nine taxa representing 42 sexual ascomycetes, 55 asexual taxa and two basidiomycetes were identified from 959 fungal collections recorded from 400 submerged samples. Samples were randomly collected from the River Nile, in Sohag, Egypt in the winter and summer between December 2010 and August 2014. Fifty-eight taxa (22 sexual ascomycetes and 36 asexual taxa) were collected during winter, while 60 taxa (25 sexual ascomycetes, 33 asexual taxa and two basidiomycetes) were collected in summer season. Of the 99 taxa recorded, 50 are new records for Egypt, including five new genera and 30 new species., Three new genera and ten new species were described in previous articles. Fungi recorded from the two seasons were markedly different, with only 19 species common to both winter and summer collections. Asexual fungi dominated the fungal community during the two seasons. Taxonomical placements of 33 species were confirmed by molecular data based on LSU and SSU rDNA genes. -
A Molecular Re-Appraisal of Taxa in the Sordariomycetidae and a New Species of Rimaconus from New Zealand
available online at www.studiesinmycology.org StudieS in Mycology 68: 203–210. 2011. doi:10.3114/sim.2011.68.09 A molecular re-appraisal of taxa in the Sordariomycetidae and a new species of Rimaconus from New Zealand S.M. Huhndorf1* and A.N. Miller2 1Field Museum of Natural History, Botany Department, Chicago, Illinois 60605–2496, USA; 2University of Illinois, Illinois Natural History Survey, Champaign, Illinois 61820-6970, USA *Correspondence: Sabine M. Huhndorf, [email protected] Abstract: Several taxa that share similar ascomatal and ascospore characters occur in monotypic or small genera throughout the Sordariomycetidae with uncertain relationships based on their morphology. Taxa in the genera Duradens, Leptosporella, Linocarpon, and Rimaconus share similar morphologies of conical ascomata, carbonised peridia and elongate ascospores, while taxa in the genera Caudatispora, Erythromada and Lasiosphaeriella possess clusters of superficial, obovoid ascomata with variable ascospores. Phylogenetic analyses of 28S large-subunit nrDNA sequences were used to test the monophyly of these genera and provide estimates of their relationships within the Sordariomycetidae. Rimaconus coronatus is described as a new species from New Zealand; it clusters with the type species, R. jamaicensis. Leptosporella gregaria is illustrated and a description is provided for this previously published taxon that is the type species and only sequenced representative of the genus. Both of these genera occur in separate, well-supported clades among taxa that form unsupported groups near the Chaetosphaeriales and Helminthosphaeriaceae. Lasiosphaeriella and Linocarpon appear to be polyphyletic with species occurring in several clades throughout the subclass. Caudatispora and Erythromada represented by single specimens and two putative Duradens spp. -
Molecular Systematics of the Sordariales: the Order and the Family Lasiosphaeriaceae Redefined
Mycologia, 96(2), 2004, pp. 368±387. q 2004 by The Mycological Society of America, Lawrence, KS 66044-8897 Molecular systematics of the Sordariales: the order and the family Lasiosphaeriaceae rede®ned Sabine M. Huhndorf1 other families outside the Sordariales and 22 addi- Botany Department, The Field Museum, 1400 S. Lake tional genera with differing morphologies subse- Shore Drive, Chicago, Illinois 60605-2496 quently are transferred out of the order. Two new Andrew N. Miller orders, Coniochaetales and Chaetosphaeriales, are recognized for the families Coniochaetaceae and Botany Department, The Field Museum, 1400 S. Lake Shore Drive, Chicago, Illinois 60605-2496 Chaetosphaeriaceae respectively. The Boliniaceae is University of Illinois at Chicago, Department of accepted in the Boliniales, and the Nitschkiaceae is Biological Sciences, Chicago, Illinois 60607-7060 accepted in the Coronophorales. Annulatascaceae and Cephalothecaceae are placed in Sordariomyce- Fernando A. FernaÂndez tidae inc. sed., and Batistiaceae is placed in the Euas- Botany Department, The Field Museum, 1400 S. Lake Shore Drive, Chicago, Illinois 60605-2496 comycetes inc. sed. Key words: Annulatascaceae, Batistiaceae, Bolini- aceae, Catabotrydaceae, Cephalothecaceae, Ceratos- Abstract: The Sordariales is a taxonomically diverse tomataceae, Chaetomiaceae, Coniochaetaceae, Hel- group that has contained from seven to 14 families minthosphaeriaceae, LSU nrDNA, Nitschkiaceae, in recent years. The largest family is the Lasiosphaer- Sordariaceae iaceae, which has contained between 33 and 53 gen- era, depending on the chosen classi®cation. To de- termine the af®nities and taxonomic placement of INTRODUCTION the Lasiosphaeriaceae and other families in the Sor- The Sordariales is one of the most taxonomically di- dariales, taxa representing every family in the Sor- verse groups within the Class Sordariomycetes (Phy- dariales and most of the genera in the Lasiosphaeri- lum Ascomycota, Subphylum Pezizomycotina, ®de aceae were targeted for phylogenetic analysis using Eriksson et al 2001). -
Calabon MS, Hyde KD, Jones EBG, Chandrasiri S, Dong W, Fryar SC, Yang J, Luo ZL, Lu YZ, Bao DF, Boonmee S
Asian Journal of Mycology 3(1): 419–445 (2020) ISSN 2651-1339 www.asianjournalofmycology.org Article Doi 10.5943/ajom/3/1/14 www.freshwaterfungi.org, an online platform for the taxonomic classification of freshwater fungi Calabon MS1,2,3, Hyde KD1,2,3, Jones EBG3,5,6, Chandrasiri S1,2,3, Dong W1,3,4, Fryar SC7, Yang J1,2,3, Luo ZL8, Lu YZ9, Bao DF1,4 and Boonmee S1,2* 1Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 2School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand 3Mushroom Research Foundation, 128 M.3 Ban Pa Deng T. Pa Pae, A. Mae Taeng, Chiang Mai 50150, Thailand 4Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai 50200, Thailand 5Department of Botany and Microbiology, College of Science, King Saud University, P.O Box 2455, Riyadh 11451, Kingdom of Saudi Arabia 633B St Edwards Road, Southsea, Hants., PO53DH, UK 7College of Science and Engineering, Flinders University, GPO Box 2100, Adelaide SA 5001, Australia 8College of Agriculture and Biological Sciences, Dali University, Dali 671003, People’s Republic of China 9School of Pharmaceutical Engineering, Guizhou Institute of Technology, Guiyang, 550003, Guizhou, People’s Republic of China Calabon MS, Hyde KD, Jones EBG, Chandrasiri S, Dong W, Fryar SC, Yang J, Luo ZL, Lu YZ, Bao DF, Boonmee S. 2020 – www.freshwaterfungi.org, an online platform for the taxonomic classification of freshwater fungi. Asian Journal of Mycology 3(1), 419–445, Doi 10.5943/ajom/3/1/14 Abstract The number of extant freshwater fungi is rapidly increasing, and the published information of taxonomic data are scattered among different online journal archives. -
A New Freshwater Ascomycete from Hong Kong Based on Morphology and Phylogeny Inferred from Rdna Gene Sequences
ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Sydowia Jahr/Year: 2005 Band/Volume: 57 Autor(en)/Author(s): Vijaykrishna Dhanasekaran, Jeewon Rajesh, Hyde Kevin D. Artikel/Article: Fusoidispora aquatica: A new freshwater ascomycete from Hong Kong based on morphology and phylogeny inferred from rDNA gene sequences. 267-280 Fusoidispora aquatics: A new freshwater ascomycete from Hong Kong based on morphology and phylogeny inferred from rDNA gene sequences Dhanasekaran Vijaykrishna*, Rajesh Jeewon & Kevin D. Hyde Centre for Research in Fungal Diversity, Department of Ecology & Biodiversity, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, PR China; *Email: [email protected] Vijaykrishna, D., R. Jeewon & Hyde K. D. (2005). Fusoidispora aquatica: A new ascomycete from Hong Kong based on morphology and phylogeny inferred from rDNA sequences. - Sydowia 57 (2): 267-280. During a survey of freshwater ascomycetes in Hong Kong, an interesting ascomycete with fusoid ascospores that had mucilaginous pads at both apices was identified. The affinities of this taxon extend between a wide range of unitunicate ascomycetes (viz. Annulatascaceae, Magaporthaceae, Pleurotremaceae, Tricho- sphaeriaceae). In order to evaluate its familial placement and generic relatedness with other known ascomycetes, partial DNA sequences derived from the large subunit ribosomal DNA (28S rDNA) were analyzed. Results from the phylogenetic analyses indicate that the family Annulatascaceae is polyphyletic. The unidentified taxon has close affinities with the Annulatascaceae and Ophiostomataceae but does not belong in any existing genera. Thus a new genus and species, Fusoidispora aquatica, is established to accommodate it. Keywords: Annulatascaceae, ascomycete, freshwater fungi, Ophiostomatales, phylogeny, 28S rDNA.