(Ascomycota) from Freshwater and Tidal Reeds
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Development and Evaluation of Rrna Targeted in Situ Probes and Phylogenetic Relationships of Freshwater Fungi
Development and evaluation of rRNA targeted in situ probes and phylogenetic relationships of freshwater fungi vorgelegt von Diplom-Biologin Christiane Baschien aus Berlin Von der Fakultät III - Prozesswissenschaften der Technischen Universität Berlin zur Erlangung des akademischen Grades Doktorin der Naturwissenschaften - Dr. rer. nat. - genehmigte Dissertation Promotionsausschuss: Vorsitzender: Prof. Dr. sc. techn. Lutz-Günter Fleischer Berichter: Prof. Dr. rer. nat. Ulrich Szewzyk Berichter: Prof. Dr. rer. nat. Felix Bärlocher Berichter: Dr. habil. Werner Manz Tag der wissenschaftlichen Aussprache: 19.05.2003 Berlin 2003 D83 Table of contents INTRODUCTION ..................................................................................................................................... 1 MATERIAL AND METHODS .................................................................................................................. 8 1. Used organisms ............................................................................................................................. 8 2. Media, culture conditions, maintenance of cultures and harvest procedure.................................. 9 2.1. Culture media........................................................................................................................... 9 2.2. Culture conditions .................................................................................................................. 10 2.3. Maintenance of cultures.........................................................................................................10 -
Molecular Systematics of the Marine Dothideomycetes
available online at www.studiesinmycology.org StudieS in Mycology 64: 155–173. 2009. doi:10.3114/sim.2009.64.09 Molecular systematics of the marine Dothideomycetes S. Suetrong1, 2, C.L. Schoch3, J.W. Spatafora4, J. Kohlmeyer5, B. Volkmann-Kohlmeyer5, J. Sakayaroj2, S. Phongpaichit1, K. Tanaka6, K. Hirayama6 and E.B.G. Jones2* 1Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, 90112, Thailand; 2Bioresources Technology Unit, National Center for Genetic Engineering and Biotechnology (BIOTEC), 113 Thailand Science Park, Paholyothin Road, Khlong 1, Khlong Luang, Pathum Thani, 12120, Thailand; 3National Center for Biothechnology Information, National Library of Medicine, National Institutes of Health, 45 Center Drive, MSC 6510, Bethesda, Maryland 20892-6510, U.S.A.; 4Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon, 97331, U.S.A.; 5Institute of Marine Sciences, University of North Carolina at Chapel Hill, Morehead City, North Carolina 28557, U.S.A.; 6Faculty of Agriculture & Life Sciences, Hirosaki University, Bunkyo-cho 3, Hirosaki, Aomori 036-8561, Japan *Correspondence: E.B. Gareth Jones, [email protected] Abstract: Phylogenetic analyses of four nuclear genes, namely the large and small subunits of the nuclear ribosomal RNA, transcription elongation factor 1-alpha and the second largest RNA polymerase II subunit, established that the ecological group of marine bitunicate ascomycetes has representatives in the orders Capnodiales, Hysteriales, Jahnulales, Mytilinidiales, Patellariales and Pleosporales. Most of the fungi sequenced were intertidal mangrove taxa and belong to members of 12 families in the Pleosporales: Aigialaceae, Didymellaceae, Leptosphaeriaceae, Lenthitheciaceae, Lophiostomataceae, Massarinaceae, Montagnulaceae, Morosphaeriaceae, Phaeosphaeriaceae, Pleosporaceae, Testudinaceae and Trematosphaeriaceae. Two new families are described: Aigialaceae and Morosphaeriaceae, and three new genera proposed: Halomassarina, Morosphaeria and Rimora. -
Fungal Diversity Driven by Bark Features Affects Phorophyte
www.nature.com/scientificreports OPEN Fungal diversity driven by bark features afects phorophyte preference in epiphytic orchids from southern China Lorenzo Pecoraro1*, Hanne N. Rasmussen2, Sofa I. F. Gomes3, Xiao Wang1, Vincent S. F. T. Merckx3, Lei Cai4 & Finn N. Rasmussen5 Epiphytic orchids exhibit varying degrees of phorophyte tree specifcity. We performed a pilot study to investigate why epiphytic orchids prefer or avoid certain trees. We selected two orchid species, Panisea unifora and Bulbophyllum odoratissimum co-occurring in a forest habitat in southern China, where they showed a specifc association with Quercus yiwuensis and Pistacia weinmannifolia trees, respectively. We analysed a number of environmental factors potentially infuencing the relationship between orchids and trees. Diference in bark features, such as water holding capacity and pH were recorded between Q. yiwuensis and P. weinmannifolia, which could infuence both orchid seed germination and fungal diversity on the two phorophytes. Morphological and molecular culture-based methods, combined with metabarcoding analyses, were used to assess fungal communities associated with studied orchids and trees. A total of 162 fungal species in 74 genera were isolated from bark samples. Only two genera, Acremonium and Verticillium, were shared by the two phorophyte species. Metabarcoding analysis confrmed the presence of signifcantly diferent fungal communities on the investigated tree and orchid species, with considerable similarity between each orchid species and its host tree, suggesting that the orchid-host tree association is infuenced by the fungal communities of the host tree bark. Epiphytism is one of the most common examples of commensalism occurring in terrestrial environments, which provides advantages, such as less competition and increased access to light, protection from terrestrial herbivores, and better fower exposure to pollinators and seed dispersal 1,2. -
Amplicon-Based Sequencing of Soil Fungi from Wood Preservative Test Sites
ORIGINAL RESEARCH published: 18 October 2017 doi: 10.3389/fmicb.2017.01997 Amplicon-Based Sequencing of Soil Fungi from Wood Preservative Test Sites Grant T. Kirker 1*, Amy B. Bishell 1, Michelle A. Jusino 2, Jonathan M. Palmer 2, William J. Hickey 3 and Daniel L. Lindner 2 1 FPL, United States Department of Agriculture-Forest Service (USDA-FS), Durability and Wood Protection, Madison, WI, United States, 2 NRS, United States Department of Agriculture-Forest Service (USDA-FS), Center for Forest Mycology Research, Madison, WI, United States, 3 Department of Soil Science, University of Wisconsin-Madison, Madison, WI, United States Soil samples were collected from field sites in two AWPA (American Wood Protection Association) wood decay hazard zones in North America. Two field plots at each site were exposed to differing preservative chemistries via in-ground installations of treated wood stakes for approximately 50 years. The purpose of this study is to characterize soil fungal species and to determine if long term exposure to various wood preservatives impacts soil fungal community composition. Soil fungal communities were compared using amplicon-based DNA sequencing of the internal transcribed spacer 1 (ITS1) region of the rDNA array. Data show that soil fungal community composition differs significantly Edited by: Florence Abram, between the two sites and that long-term exposure to different preservative chemistries National University of Ireland Galway, is correlated with different species composition of soil fungi. However, chemical analyses Ireland using ICP-OES found levels of select residual preservative actives (copper, chromium and Reviewed by: Seung Gu Shin, arsenic) to be similar to naturally occurring levels in unexposed areas. -
<I>Tothia Fuscella</I>
ISSN (print) 0093-4666 © 2011. Mycotaxon, Ltd. ISSN (online) 2154-8889 MYCOTAXON http://dx.doi.org/10.5248/118.203 Volume 118, pp. 203–211 October–December 2011 Epitypification, morphology, and phylogeny of Tothia fuscella Haixia Wu1, Walter M. Jaklitsch2, Hermann Voglmayr2 & Kevin D. Hyde1, 3, 4* 1 International Fungal Research and Development Centre, Key Laboratory of Resource Insect Cultivation & Utilization, State Forestry Administration, The Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, 650224, PR China 2 Department of Systematic and Evolutionary Botany, Faculty Centre of Biodiversity, University of Vienna, Rennweg 14, A-1030 Wien, Austria 3 School of Science, Mae Fah Luang University, Tasud, Muang, Chiang Rai 57100, Thailand 4 Botany and Microbiology Department, College of Science, King Saud University, Riyadh, 11442, Saudi Arabia *Correspondence to: [email protected] Abstract — The holotype of Tothia fuscella has been re-examined and is re-described and illustrated. An identical fresh specimen from Austria is used to designate an epitype with herbarium material and a living culture. Sequence analyses show T. fuscella to be most closely related to Venturiaceae and not Microthyriaceae, to which it was previously referred. Key words — Dothideomycetes, molecular phylogeny, taxonomy Introduction We have been re-describing and illustrating the generic types of Dothideomycetes (Zhang et al. 2008, 2009, Wu et al. 2010, 2011, Li et al. 2011) and have tried where possible to obtain fresh specimens for epitypification and use molecular analyses to provide a natural classification. Our previous studies of genera in the Microthyriaceae, a poorly known family within the Dothideomycetes, have resulted in several advances (Wu et al. -
Taxonomic Utility of Old Names in Current Fungal Classification and Nomenclature: Conflicts, Confusion & Clarifications
Mycosphere 7 (11): 1622–1648 (2016) www.mycosphere.org ISSN 2077 7019 Article – special issue Doi 10.5943/mycosphere/7/11/2 Copyright © Guizhou Academy of Agricultural Sciences Taxonomic utility of old names in current fungal classification and nomenclature: Conflicts, confusion & clarifications Dayarathne MC1,2, Boonmee S1,2, Braun U7, Crous PW8, Daranagama DA1, Dissanayake AJ1,6, Ekanayaka H1,2, Jayawardena R1,6, Jones EBG10, Maharachchikumbura SSN5, Perera RH1, Phillips AJL9, Stadler M11, Thambugala KM1,3, Wanasinghe DN1,2, Zhao Q1,2, Hyde KD1,2, Jeewon R12* 1Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 2Key Laboratory for Plant Biodiversity and Biogeography of East Asia (KLPB), Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan China3Guizhou Key Laboratory of Agricultural Biotechnology, Guizhou Academy of Agricultural Sciences, Guiyang 550006, Guizhou, China 4Engineering Research Center of Southwest Bio-Pharmaceutical Resources, Ministry of Education, Guizhou University, Guiyang 550025, Guizhou Province, China5Department of Crop Sciences, College of Agricultural and Marine Sciences, Sultan Qaboos University, P.O. Box 34, Al-Khod 123,Oman 6Institute of Plant and Environment Protection, Beijing Academy of Agriculture and Forestry Sciences, No 9 of ShuGuangHuaYuanZhangLu, Haidian District Beijing 100097, China 7Martin Luther University, Institute of Biology, Department of Geobotany, Herbarium, Neuwerk 21, 06099 Halle, Germany 8Westerdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584CT Utrecht, The Netherlands. 9University of Lisbon, Faculty of Sciences, Biosystems and Integrative Sciences Institute (BioISI), Campo Grande, 1749-016 Lisbon, Portugal. 10Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, 50200, Thailand 11Helmholtz-Zentrum für Infektionsforschung GmbH, Dept. -
Towards a Phylogenetic Clarification of Lophiostoma / Massarina and Morphologically Similar Genera in the Pleosporales
Fungal Diversity Towards a phylogenetic clarification of Lophiostoma / Massarina and morphologically similar genera in the Pleosporales Zhang, Y.1, Wang, H.K.2, Fournier, J.3, Crous, P.W.4, Jeewon, R.1, Pointing, S.B.1 and Hyde, K.D.5,6* 1Division of Microbiology, School of Biological Sciences, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, P.R. China 2Biotechnology Institute, Zhejiang University, 310029, P.R. China 3Las Muros, Rimont, Ariège, F 09420, France 4Centraalbureau voor Schimmelcultures, Fungal Biodiversity Centre, P.O. Box 85167, 3508 AD, Utrecht, The Netherlands 5School of Science, Mae Fah Luang University, Tasud, Muang, Chiang Rai 57100, Thailand 6International Fungal Research & Development Centre, The Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming, Yunnan, P.R. China 650034 Zhang, Y., Wang, H.K., Fournier, J., Crous, P.W., Jeewon, R., Pointing, S.B. and Hyde, K.D. (2009). Towards a phylogenetic clarification of Lophiostoma / Massarina and morphologically similar genera in the Pleosporales. Fungal Diversity 38: 225-251. Lophiostoma, Lophiotrema and Massarina are similar genera that are difficult to distinguish morphologically. In order to obtain a better understanding of these genera, lectotype material of the generic types, Lophiostoma macrostomum, Lophiotrema nucula and Massarina eburnea were examined and are re-described. The phylogeny of these genera is investigated based on the analysis of 26 Lophiostoma- and Massarina-like taxa and three genes – 18S, 28S rDNA and RPB2. These taxa formed five well-supported sub-clades in Pleosporales. This study confirms that both Lophiostoma and Massarina are polyphyletic. Massarina-like taxa can presently be differentiated into two groups – the Lentithecium group and the Massarina group. -
A Higher-Level Phylogenetic Classification of the Fungi
mycological research 111 (2007) 509–547 available at www.sciencedirect.com journal homepage: www.elsevier.com/locate/mycres A higher-level phylogenetic classification of the Fungi David S. HIBBETTa,*, Manfred BINDERa, Joseph F. BISCHOFFb, Meredith BLACKWELLc, Paul F. CANNONd, Ove E. ERIKSSONe, Sabine HUHNDORFf, Timothy JAMESg, Paul M. KIRKd, Robert LU¨ CKINGf, H. THORSTEN LUMBSCHf, Franc¸ois LUTZONIg, P. Brandon MATHENYa, David J. MCLAUGHLINh, Martha J. POWELLi, Scott REDHEAD j, Conrad L. SCHOCHk, Joseph W. SPATAFORAk, Joost A. STALPERSl, Rytas VILGALYSg, M. Catherine AIMEm, Andre´ APTROOTn, Robert BAUERo, Dominik BEGEROWp, Gerald L. BENNYq, Lisa A. CASTLEBURYm, Pedro W. CROUSl, Yu-Cheng DAIr, Walter GAMSl, David M. GEISERs, Gareth W. GRIFFITHt,Ce´cile GUEIDANg, David L. HAWKSWORTHu, Geir HESTMARKv, Kentaro HOSAKAw, Richard A. HUMBERx, Kevin D. HYDEy, Joseph E. IRONSIDEt, Urmas KO˜ LJALGz, Cletus P. KURTZMANaa, Karl-Henrik LARSSONab, Robert LICHTWARDTac, Joyce LONGCOREad, Jolanta MIA˛ DLIKOWSKAg, Andrew MILLERae, Jean-Marc MONCALVOaf, Sharon MOZLEY-STANDRIDGEag, Franz OBERWINKLERo, Erast PARMASTOah, Vale´rie REEBg, Jack D. ROGERSai, Claude ROUXaj, Leif RYVARDENak, Jose´ Paulo SAMPAIOal, Arthur SCHU¨ ßLERam, Junta SUGIYAMAan, R. Greg THORNao, Leif TIBELLap, Wendy A. UNTEREINERaq, Christopher WALKERar, Zheng WANGa, Alex WEIRas, Michael WEISSo, Merlin M. WHITEat, Katarina WINKAe, Yi-Jian YAOau, Ning ZHANGav aBiology Department, Clark University, Worcester, MA 01610, USA bNational Library of Medicine, National Center for Biotechnology Information, -
An Evaluation of the Monophyly of Massarina Based on Ribosomal DNA Sequences
~\.l~rolo,~~,94(5), 2002, pp 803-813 O 2002 b\ The M\cological Socieh of Ame~ica,La~rence, KS 660448895 An evaluation of the monophyly of Massarina based on ribosomal DNA sequences Edward C. Y. Liew cies were included in Massam'na, the first being Mas- Centre for Research in Fungal Diversity, Department of sam'na eburnea (Tul. & C. Tul.) Sacc., but a type was Ecology & Biodiversity, The CTniversityof Hong Kong, not indicated, nor was the genus placed in a family. Pokfulam Road, Hong Kong SAR, PR China Massam'na eburnea was later selected as lectotype of Andre Aptroot this genus by Clements and Shear (1957) and was Centraalbureau voor Schimmelcultures, P 0. Box redescribed and illustrated by Hyde (1995a). 85167, NL-3508 AD Utrecht, The Netherlnnds A new family, the Massarinaceae Munk, was intro- Kevin D. Hydel duced by Munk (1956) to accommodate Massam'na. This family was accepted by various authors (Eriksson Centle for Research zn Fungal Dzverszty, Department of Ecolqg & Bzodzversztj, The Unzverszty of Hong Kong 1981, 1982, Eriksson and Hawksworth 1985). Bose Pokfulam Road, Hong Kong SAR, PR Chzna (1961), in his review of Massam'na, noted that doubts had previously been expressed several times about whether the introduction of a new family was justified Abstract: The monophyletic status of the genus (Holm et a1 1957, Scheinpflug 1958).He subsequent- Massam'na was evaluated on the basis of phylogenetic ly placed Massam'na in the existing Pleosporaceae, analysis of the partial small subunit gene (SSU), in- due to the lack of distinctive characters distinguish- ternal transcribed spacers (ITS 1 & 2), and 5.8s gene ing the two families. -
The Genus Pseudodidymosphaeria
Asian Journal of Mycology 1(1): 1–8 (2018) ISSN TBA www.asianjournalofmycology.org Article Doi 10.5943/ajom/1/1/1 Copyright © Mushroom Research Foundation The genus Pseudodidymosphaeria Thambugala KM1, Peršoh D2, Perera RH1 and Hyde KD1 1Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 2Geobotany, Ruhr-Universität Bochum, Universitätsstraße 150, 44780 Bochum, Germany Thambugala KM, Peršoh D, Perera RH, Hyde KD 2018 – The genus Pseudodidymosphaeria. Asian Journal of Mycology 1(1), 1–8, Doi 10.5943/ajom/1/1/1 Abstract The genus Pseudodidymosphaeria is revisited with an overview of its history, a generic description with amendments and notes and illustrations of the genus. Molecular data from two species of the genus are analyzed using single and combined ITS and LSU gene datasets and the workflow of phylogenetic analysis is provided in an appendix. The genus Pseudodidymosphaeria formed a well-supported clade in the family Massarinaceae. Key words – ARB – ITS – LSU – Massarinaceae – Poaceae Introduction The family Massarinaceae was established to accommodate four genera, Keissleriella, Massarina, Metasphaeria, Pseudotrichia, and Trichometasphaeria (Munk 1956). Barr (1987) treated Massarinaceae as a synonym of Lophiostomataceae. However, these two families are now recognized as separate lineages in Pleosporales, Dothideomycetes (Zhang et al. 2012, Hyde et al. 2013, Thambugala et al. 2015b, Wijayawardene et al. 2018). During the past 60 years many genera were included or removed from Massarinaceae depending on the various taxonomic treatments and accessibility of sequence data (Zhang et al. 2012, Hyde et al. 2013, Wijayawardene et al. 2014, 2017, Tanaka et al. 2015, Thambugala et al. -
Saprobic Fungi on Wood and Litter of Alnus Alnobetula in the Swiss Alps
Saprobic fungi on wood and litter of Alnus alnobetula in the Swiss Alps BEATRICE SENN-IRLET* WSL, Swiss Federal Research Institute, Zürcherstrasse 111, CH – 8903 Bimensdorf, Switzerland ROLF MÜRNER Naturmuseum, Kasernenplatz 6, CH – 6003 Luzern, Switzerland ELIA MARTINI Sentiero per Sécc, CH – 6676 Bignasco, Switzerland NICOLAS KÜFFER tuttifunghi, Bahnstrasse 22, CH – 3008 Bern, Switzerland ROMANO DE MARCHI Bühlackerweg 33, CH – 8405 Winterthur, Switzerland GUIDO BIERI tuttifunghi, Bahnstrasse 22, CH- 3008 Bern, Switzerland *Correspondence to: [email protected] ABSTRACT — 246 species representing 73 genera and 90 species of ascomycetes, basidiomycetes being represented with 44 genera of aphyllophoralean fungi with 77 species, 23 genera of agarics with 68 species and 8 genera of tremelloid fungi with 12 species growing on wood and litter of Alnus alnobetula in Switzerland are given. Clitocybe and Mycena species dominate among the leaf litter inhabiting species. Fallen branches have the highest species diversity. The host-specific Peniophora aurantiaca is one of the most conspicuous and most frequent species. KEY WORDS — lignicolous and foliicolous fungi, diversity, subalpine alder stand Introduction Bush-like Green alder (Alnus alnobetula (Ehrh.) K. Koch, syn. Alnus viridis (Chaix) DC. aggr., Betulaceae) is present in subarctic and in some subalpine vegetation types of the Northern Hemisphere. In the Alps two forms exist, Alnus alnobetula s.str. and Alnus alnobetula ssp. brembana (Rota) H.J.P. Winkl. with smaller leaves. Green alder is an early successional shrub that invades screes, avalanche slide paths and pastures in the subalpine zone of the Alpine, Carpathian and Dinaric chains in Europe. In the Western Alps, Green alder stands (Alnetum viridis Br.-Bl.) are widely spread at an altitude of 1000–2000 m, in Switzerland MYCOTAXON link page 120: 506 Expert reviewers: Cvetomir M. -
Pseudodidymosphaeria Gen. Nov. in Massarinaceae
Phytotaxa 231 (3): 271–282 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2015 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.231.3.5 Pseudodidymosphaeria gen. nov. in Massarinaceae KASUN M. THAMBUGALA1, 2, 3, YU CHUNFANG4, ERIO CAMPORESI5, ALI H. BAHKALI6, ZUO-YI LIU1, * & KEVIN D. HYDE2, 3 1Guizhou Key Laboratory of Agricultural Biotechnology, Guizhou Academy of Agricultural Sciences, Xiaohe District, Guiyang City, Guizhou Province 550006, People’s Republic of China 2Institute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 3School of Science, Mae Fah Luang University, Chiang Rai. 57100, Thailand 4Institute of Basic Medical Sciences, Hubei University of Medicine, shiyan, Hubei Province, 442000, People’s Republic of China 5A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy; A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314, Brescia, Italy 6Department of Botany and Microbiology, King Saudi University, Riyadh, Saudi Arabia *Corresponding author: email: [email protected] Abstract Didymosphaeria spartii was collected from dead branches of Spartium junceum in Italy. Multi-gene phylogenetic analyses of ITS, 18S and 28S nrDNA sequence data were carried out using maximum likelihood and Bayesian analysis. The resulting phylogenetic trees showed this to be a new genus in a well-supported clade in Massarinaceae. A new genus Pseudodidymo- sphaeria is therefore introduced to accommodate this species based on molecular phylogeny and morphology. A illustrated account is provided for the new genus with its asexual morph and the new taxon is compared with Massarina and Didymo- sphaeria.