AR TICLE New Combinations of Plant-Associated Fungi Resulting
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Biology and Management of the Dutch Elm Disease Vector, Hylurgopinus Rufipes Eichhoff (Coleoptera: Curculionidae) in Manitoba By
Biology and Management of the Dutch Elm Disease Vector, Hylurgopinus rufipes Eichhoff (Coleoptera: Curculionidae) in Manitoba by Sunday Oghiakhe A thesis submitted to the Faculty of Graduate Studies of The University of Manitoba in partial fulfilment of the requirements of the degree of Doctor of Philosophy Department of Entomology University of Manitoba Winnipeg Copyright © 2014 Sunday Oghiakhe Abstract Hylurgopinus rufipes, the native elm bark beetle (NEBB), is the major vector of Dutch elm disease (DED) in Manitoba. Dissections of American elms (Ulmus americana), in the same year as DED symptoms appeared in them, showed that NEBB constructed brood galleries in which a generation completed development, and adult NEBB carrying DED spores would probably leave the newly-symptomatic trees. Rapid removal of freshly diseased trees, completed by mid-August, will prevent spore-bearing NEBB emergence, and is recommended. The relationship between presence of NEBB in stained branch sections and the total number of NEEB per tree could be the basis for methods to prioritize trees for rapid removal. Numbers and densities of overwintering NEBB in elm trees decreased with increasing height, with >70% of the population overwintering above ground doing so in the basal 15 cm. Substantial numbers of NEBB overwinter below the soil surface, and could be unaffected by basal spraying. Mark-recapture studies showed that frequency of spore bearing by overwintering beetles averaged 45% for the wild population and 2% for marked NEBB released from disease-free logs. Most NEBB overwintered close to their emergence site, but some traveled ≥4.8 km before wintering. Studies comparing efficacy of insecticides showed that chlorpyrifos gave 100% control of overwintering NEBB for two years as did bifenthrin: however, permethrin and carbaryl provided transient efficacy. -
Patellariaceae Revisited
Mycosphere 6 (3): 290–326(2015) ISSN 2077 7019 www.mycosphere.org Article Mycosphere Copyright © 2015 Online Edition Doi 10.5943/mycosphere/6/3/7 Patellariaceae revisited Yacharoen S1,2, Tian Q1,2, Chomnunti P1,2, Boonmee S1, Chukeatirote E2, Bhat JD3 and Hyde KD1,2,4,5* 1Institute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand 2School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand 3Formerly at Department of Botany, Goa University, Goa 403 206, India 4Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, China 5World Agroforestry Centre, East and Central Asia, Kunming 650201, Yunnan, China Yacharoen S, Tian Q, Chomnunti P, Boonmee S, Chukeatirote E, Bhat JD, Hyde KD 2015 – Patellariaceae revisited. Mycosphere 6(3), 290–326, Doi 10.5943/mycosphere/6/3/7 Abstract The Dothideomycetes include several genera whose ascomata can be considered as apothecia and thus would be grouped as discomycetes. Most genera are grouped in the family Patellariaceae, but also Agrynnaceae and other families. The Hysteriales include genera having hysterioid ascomata and can be confused with species in Patellariaceae with discoid apothecia if the opening is wide enough. In this study, genera of the family Patellariaceae were re-examined and characterized based on morphological examination. As a result of this study the genera Baggea, Endotryblidium, Holmiella, Hysteropatella, Lecanidiella, Lirellodisca, Murangium, Patellaria, Poetschia, Rhizodiscina, Schrakia, Stratisporella and Tryblidaria are retained in the family Patellariaceae. The genera Banhegyia, Pseudoparodia and Rhytidhysteron are excluded because of differing morphology and/or molecular data. -
Estrategias De Manejo De La Roña Cladosporium Cladosporioides (FRESEN) G.A
Estrategias de Manejo de la Roña Cladosporium cladosporioides (FRESEN) G.A. de VRIES de la Gulupa Passiflora edulis f. edulis Sims. Carlos Fernando Castillo Londoño Universidad Nacional de Colombia Facultad de Ciencias Agropecuarias Maestría en Ciencias Agrarias Palmira, 2014 Estrategias de Manejo de la Roña Cladosporium cladosporioides (FRESEN) G.A. de VRIES de la Gulupa Passiflora edulis f. edulis Sims. Carlos Fernando Castillo Londoño Trabajo de investigación presentado como requisito parcial para optar al título de: Magister en Ciencias Agrarias con énfasis en Fitopatología Director: Ph.D. Carlos German Muñoz Perea Codirector: Ph.D. Elizabeth Álvarez Codirector: Ph.D. Kriss Wichechkus Universidad Nacional de Colombia Facultad de Ciencias Agropecuarias Maestría en Ciencias Agrarias Palmira. 2014 A Dios por darme la inmensa voluntad y capacidad de entrega para la hacer las cosas con amor y dedicación. A mi madre Carmen y a Geovanny por su gran confianza, apoyo, consejos y su constante exigencia para formar la persona que soy. AGRADECIMIENTOS A la Universidad Nacional de Colombia sede Palmira por las oportunidades y facilidades brindadas en el transcurso de mi carrera profesional. A la Universidad Jorge Tadeo Lozano y al Centro Internacional de Agricultura Tropical (CIAT) por brindarme la oportunidad de trabajar en el proyecto. A mi director Carlos German Muñoz, y codirectores Elizabeth Álvarez y Kriss Wichechkus, por sus valiosos aportes y orientación en esta investigación. A la Dra. Martha Cárdenas directora del Centro de Transformación Genética (Riverside), por su valiosa colaboración en la revisión del documento. A mis profesores, a quienes les debo gran parte de mis conocimientos, gracias por prepararnos para un futuro competitivo no solo como los mejores profesionales sino también como mejores personas. -
Competing Sexual and Asexual Generic Names in <I
doi:10.5598/imafungus.2018.09.01.06 IMA FUNGUS · 9(1): 75–89 (2018) Competing sexual and asexual generic names in Pucciniomycotina and ARTICLE Ustilaginomycotina (Basidiomycota) and recommendations for use M. Catherine Aime1, Lisa A. Castlebury2, Mehrdad Abbasi1, Dominik Begerow3, Reinhard Berndt4, Roland Kirschner5, Ludmila Marvanová6, Yoshitaka Ono7, Mahajabeen Padamsee8, Markus Scholler9, Marco Thines10, and Amy Y. Rossman11 1Purdue University, Department of Botany and Plant Pathology, West Lafayette, IN 47901, USA; corresponding author e-mail: maime@purdue. edu 2Mycology & Nematology Genetic Diversity and Biology Laboratory, USDA-ARS, Beltsville, MD 20705, USA 3Ruhr-Universität Bochum, Geobotanik, ND 03/174, D-44801 Bochum, Germany 4ETH Zürich, Plant Ecological Genetics, Universitätstrasse 16, 8092 Zürich, Switzerland 5Department of Biomedical Sciences and Engineering, National Central University, 320 Taoyuan City, Taiwan 6Czech Collection of Microoorganisms, Faculty of Science, Masaryk University, 625 00 Brno, Czech Republic 7Faculty of Education, Ibaraki University, Mito, Ibaraki 310-8512, Japan 8Systematics Team, Manaaki Whenua Landcare Research, Auckland 1072, New Zealand 9Staatliches Museum f. Naturkunde Karlsruhe, Erbprinzenstr. 13, D-76133 Karlsruhe, Germany 10Senckenberg Gesellschaft für Naturforschung, Frankfurt (Main), Germany 11Department of Botany & Plant Pathology, Oregon State University, Corvallis, OR 97333, USA Abstract: With the change to one scientific name for pleomorphic fungi, generic names typified by sexual and Key words: asexual morphs have been evaluated to recommend which name to use when two names represent the same genus Basidiomycetes and thus compete for use. In this paper, generic names in Pucciniomycotina and Ustilaginomycotina are evaluated pleomorphic fungi based on their type species to determine which names are synonyms. Twenty-one sets of sexually and asexually taxonomy typified names in Pucciniomycotina and eight sets in Ustilaginomycotina were determined to be congeneric and protected names compete for use. -
Phaeoseptaceae, Pleosporales) from China
Mycosphere 10(1): 757–775 (2019) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/10/1/17 Morphological and phylogenetic studies of Pleopunctum gen. nov. (Phaeoseptaceae, Pleosporales) from China Liu NG1,2,3,4,5, Hyde KD4,5, Bhat DJ6, Jumpathong J3 and Liu JK1*,2 1 School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, P.R. China 2 Guizhou Key Laboratory of Agricultural Biotechnology, Guizhou Academy of Agricultural Sciences, Guiyang 550006, P.R. China 3 Faculty of Agriculture, Natural Resources and Environment, Naresuan University, Phitsanulok 65000, Thailand 4 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 5 Mushroom Research Foundation, Chiang Rai 57100, Thailand 6 No. 128/1-J, Azad Housing Society, Curca, P.O., Goa Velha 403108, India Liu NG, Hyde KD, Bhat DJ, Jumpathong J, Liu JK 2019 – Morphological and phylogenetic studies of Pleopunctum gen. nov. (Phaeoseptaceae, Pleosporales) from China. Mycosphere 10(1), 757–775, Doi 10.5943/mycosphere/10/1/17 Abstract A new hyphomycete genus, Pleopunctum, is introduced to accommodate two new species, P. ellipsoideum sp. nov. (type species) and P. pseudoellipsoideum sp. nov., collected from decaying wood in Guizhou Province, China. The genus is characterized by macronematous, mononematous conidiophores, monoblastic conidiogenous cells and muriform, oval to ellipsoidal conidia often with a hyaline, elliptical to globose basal cell. Phylogenetic analyses of combined LSU, SSU, ITS and TEF1α sequence data of 55 taxa were carried out to infer their phylogenetic relationships. The new taxa formed a well-supported subclade in the family Phaeoseptaceae and basal to Lignosphaeria and Thyridaria macrostomoides. -
Mycosphere Notes 225–274: Types and Other Specimens of Some Genera of Ascomycota
Mycosphere 9(4): 647–754 (2018) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/9/4/3 Copyright © Guizhou Academy of Agricultural Sciences Mycosphere Notes 225–274: types and other specimens of some genera of Ascomycota Doilom M1,2,3, Hyde KD2,3,6, Phookamsak R1,2,3, Dai DQ4,, Tang LZ4,14, Hongsanan S5, Chomnunti P6, Boonmee S6, Dayarathne MC6, Li WJ6, Thambugala KM6, Perera RH 6, Daranagama DA6,13, Norphanphoun C6, Konta S6, Dong W6,7, Ertz D8,9, Phillips AJL10, McKenzie EHC11, Vinit K6,7, Ariyawansa HA12, Jones EBG7, Mortimer PE2, Xu JC2,3, Promputtha I1 1 Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand 2 Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, 132 Lanhei Road, Kunming 650201, China 3 World Agro Forestry Centre, East and Central Asia, 132 Lanhei Road, Kunming 650201, Yunnan Province, People’s Republic of China 4 Center for Yunnan Plateau Biological Resources Protection and Utilization, College of Biological Resource and Food Engineering, Qujing Normal University, Qujing, Yunnan 655011, China 5 Shenzhen Key Laboratory of Microbial Genetic Engineering, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China 6 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 7 Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai 50200, Thailand 8 Department Research (BT), Botanic Garden Meise, Nieuwelaan 38, BE-1860 Meise, Belgium 9 Direction Générale de l'Enseignement non obligatoire et de la Recherche scientifique, Fédération Wallonie-Bruxelles, Rue A. -
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. -
Preliminary Classification of Leotiomycetes
Mycosphere 10(1): 310–489 (2019) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/10/1/7 Preliminary classification of Leotiomycetes Ekanayaka AH1,2, Hyde KD1,2, Gentekaki E2,3, McKenzie EHC4, Zhao Q1,*, Bulgakov TS5, Camporesi E6,7 1Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, Yunnan, China 2Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand 3School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand 4Landcare Research Manaaki Whenua, Private Bag 92170, Auckland, New Zealand 5Russian Research Institute of Floriculture and Subtropical Crops, 2/28 Yana Fabritsiusa Street, Sochi 354002, Krasnodar region, Russia 6A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy. 7A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314 Brescia, Italy. Ekanayaka AH, Hyde KD, Gentekaki E, McKenzie EHC, Zhao Q, Bulgakov TS, Camporesi E 2019 – Preliminary classification of Leotiomycetes. Mycosphere 10(1), 310–489, Doi 10.5943/mycosphere/10/1/7 Abstract Leotiomycetes is regarded as the inoperculate class of discomycetes within the phylum Ascomycota. Taxa are mainly characterized by asci with a simple pore blueing in Melzer’s reagent, although some taxa have lost this character. The monophyly of this class has been verified in several recent molecular studies. However, circumscription of the orders, families and generic level delimitation are still unsettled. This paper provides a modified backbone tree for the class Leotiomycetes based on phylogenetic analysis of combined ITS, LSU, SSU, TEF, and RPB2 loci. In the phylogenetic analysis, Leotiomycetes separates into 19 clades, which can be recognized as orders and order-level clades. -
Elsevier Editorial System(Tm) for Fungal Ecology Manuscript Draft
Elsevier Editorial System(tm) for Fungal Ecology Manuscript Draft Manuscript Number: FUNECO-D-16-00203R1 Title: Intra-diurnal and daily changes in Didymella ascospore concentrations in the air of an urban site Article Type: Original Research Paper Keywords: pathogen; bioaerosol; asthma; exposure time; air quality; fungal ecology Corresponding Author: Dr. Magdalena Sadyś, Ph.D. Corresponding Author's Institution: Rothamsted Research First Author: Magdalena Sadyś, Ph.D. Order of Authors: Magdalena Sadyś, Ph.D.; Jonathan S West, Ph.D. Abstract: Didymella sp. is a common plant pathogen affecting mainly cereal crops in countries with temperate climates, and its airborne spores are also a potential human allergen. A 5-year monitoring study was carried out at an urban site in the UK to establish the most likely exposure time in order to alert people sensitised to spores of this genus. Didymella ascospores occurred in air with a bimodal pattern, with peak concentrations occurring at 03:00 and 22:00. The majority of ascospores were observed from 20:30 to 07:30 according to a multivariate regression tree analysis. Similarly, circular tests indicated that the maximum hourly concentrations were found in the morning hours. The highest ascospore concentrations were observed in very humid conditions occurring after rainfall. The observations taken from an urban site were delayed in relation to the time of ascospore release previously reported from field sites. Thus, there is a high possibility of regional transport of ascospores in the atmosphere from remote sources. Cover Letter Intra-diurnal and daily changes in Didymella ascospore concentrations in the air of an urban site Magdalena Sadyś 1,2 , Jonathan S. -
New Records of Pyrenomycetes from the Czech and Slovak Republics II Some Rare and Interesting Species of the Orders Dothideales and Sordariales
C z e c h m y c o l . 49 (3-4), 1997 New records of Pyrenomycetes from the Czech and Slovak Republics II Some rare and interesting species of the orders Dothideales and Sordariales M a r t in a R é b l o v á 1 and M irk o S v r č e k 2 institute of Botany, Academy of Sciences, 252 43 Průhonice, Czech Republic 2 Department of Mycology, National Museum, Václavské nám. 68, 1X5 79 Praha, Czech Republic Réblová M. and Svrček M. (1997): New records of Pyrenomycetes from the Czech and Slovak Republics II. Some rare and interesting species of the orders Dothideales and Sordariales.- Czech Mycol. 49: 207-227 The paper deals with X2 lignicolous species of Pyrenomycetes; Actidium hysterioides Fr., Actidium nitidum (Cooke et Ellis) Zogg, Capronia borealis M. E. Barr, Capronia chlorospora (Ellis et Everh.) M. E. Barr, Cercophora caudata (Currey) Lundq., Farlowiella carmichaelina (Berk.) Sacc., Gloniopsis curvata (Fr.) Sacc., Mytilinidion rhenanum Fuckel, Pseudotrichia m utabilis (Pers.: Fr.) Wehm., Rebentischia massalongii (Mont.) Sacc., Trematosphaeria fissa (Fuckel) Winter and Trematosphaeria morthieri Fuckel, most of which are reported from the Czech and Slovak Republics for the first time. Species are listed with localities, descriptions, illustrations and taxonomical and ecological notes. Most of them occur rarely in both countries or have very interesting habitats. Capronia borealis and Capronia chlorospora, so far known only from the temperate zone of North America, are reported from Europe for the first time. The systematic position of these species is arranged according to Eriksson and Hawksworth (1993). -
Color Plates
Color Plates Plate 1 (a) Lethal Yellowing on Coconut Palm caused by a Phytoplasma Pathogen. (b, c) Tulip Break on Tulip caused by Lily Latent Mosaic Virus. (d, e) Ringspot on Vanda Orchid caused by Vanda Ringspot Virus R.K. Horst, Westcott’s Plant Disease Handbook, DOI 10.1007/978-94-007-2141-8, 701 # Springer Science+Business Media Dordrecht 2013 702 Color Plates Plate 2 (a, b) Rust on Rose caused by Phragmidium mucronatum.(c) Cedar-Apple Rust on Apple caused by Gymnosporangium juniperi-virginianae Color Plates 703 Plate 3 (a) Cedar-Apple Rust on Cedar caused by Gymnosporangium juniperi.(b) Stunt on Chrysanthemum caused by Chrysanthemum Stunt Viroid. Var. Dark Pink Orchid Queen 704 Color Plates Plate 4 (a) Green Flowers on Chrysanthemum caused by Aster Yellows Phytoplasma. (b) Phyllody on Hydrangea caused by a Phytoplasma Pathogen Color Plates 705 Plate 5 (a, b) Mosaic on Rose caused by Prunus Necrotic Ringspot Virus. (c) Foliar Symptoms on Chrysanthemum (Variety Bonnie Jean) caused by (clockwise from upper left) Chrysanthemum Chlorotic Mottle Viroid, Healthy Leaf, Potato Spindle Tuber Viroid, Chrysanthemum Stunt Viroid, and Potato Spindle Tuber Viroid (Mild Strain) 706 Color Plates Plate 6 (a) Bacterial Leaf Rot on Dieffenbachia caused by Erwinia chrysanthemi.(b) Bacterial Leaf Rot on Philodendron caused by Erwinia chrysanthemi Color Plates 707 Plate 7 (a) Common Leafspot on Boston Ivy caused by Guignardia bidwellii.(b) Crown Gall on Chrysanthemum caused by Agrobacterium tumefaciens 708 Color Plates Plate 8 (a) Ringspot on Tomato Fruit caused by Cucumber Mosaic Virus. (b, c) Powdery Mildew on Rose caused by Podosphaera pannosa Color Plates 709 Plate 9 (a) Late Blight on Potato caused by Phytophthora infestans.(b) Powdery Mildew on Begonia caused by Erysiphe cichoracearum.(c) Mosaic on Squash caused by Cucumber Mosaic Virus 710 Color Plates Plate 10 (a) Dollar Spot on Turf caused by Sclerotinia homeocarpa.(b) Copper Injury on Rose caused by sprays containing Copper. -
Novel Species of Huntiella from Naturally-Occurring Forest Trees in Greece and South Africa
A peer-reviewed open-access journal MycoKeys 69: 33–52 (2020) Huntiella species in Greece and South Africa 33 doi: 10.3897/mycokeys.69.53205 RESEARCH ARTICLE MycoKeys http://mycokeys.pensoft.net Launched to accelerate biodiversity research Novel species of Huntiella from naturally-occurring forest trees in Greece and South Africa FeiFei Liu1,2, Seonju Marincowitz1, ShuaiFei Chen1,2, Michael Mbenoun1, Panaghiotis Tsopelas3, Nikoleta Soulioti3, Michael J. Wingfield1 1 Department of Biochemistry, Genetics and Microbiology (BGM), Forestry and Agricultural Biotechnology In- stitute (FABI), University of Pretoria, Pretoria 0028, South Africa 2 China Eucalypt Research Centre (CERC), Chinese Academy of Forestry (CAF), ZhanJiang, 524022, GuangDong Province, China 3 Institute of Mediter- ranean Forest Ecosystems, Terma Alkmanos, 11528 Athens, Greece Corresponding author: ShuaiFei Chen ([email protected]) Academic editor: R. Phookamsak | Received 13 April 2020 | Accepted 4 June 2020 | Published 10 July 2020 Citation: Liu FF, Marincowitz S, Chen SF, Mbenoun M, Tsopelas P, Soulioti N, Wingfield MJ (2020) Novel species of Huntiella from naturally-occurring forest trees in Greece and South Africa. MycoKeys 69: 33–52. https://doi. org/10.3897/mycokeys.69.53205 Abstract Huntiella species are wood-infecting, filamentous ascomycetes that occur in fresh wounds on a wide va- riety of tree species. These fungi are mainly known as saprobes although some have been associated with disease symptoms. Six fungal isolates with typical culture characteristics of Huntiella spp. were collected from wounds on native forest trees in Greece and South Africa. The aim of this study was to identify these isolates, using morphological characters and multigene phylogenies of the rRNA internal transcribed spacer (ITS) region, portions of the β-tubulin (BT1) and translation elongation factor 1α (TEF-1α) genes.