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Showing papers by "Celeste C. Linde published in 2020"


Journal ArticleDOI
Pedro W. Crous1, D. A. Cowan1, G. Maggs-Kölling, Neriman Yilmaz1, Ellen Larsson2, Claudio Angelini3, Tor Erik Brandrud, John Dearnaley4, Bálint Dima5, Francesco Dovana6, Nigel Fechner, Dania García7, Josepa Gené7, Roy E. Halling8, Jos Houbraken, P. Leonard, J. Jennifer Luangsa-ard9, W. Noisripoom9, A. E. Rea-Ireland10, Hana Ševčíková, Christopher W. Smyth11, Alfredo Vizzini6, J. D. Adam12, G. C. Adams13, A. V. Alexandrova14, A. Alizadeh15, E. Alvarez Duarte16, Vera Andjic, Vladimír Antonín, Francisco Arenas17, R. Assabgui18, Josep Ballarà, A. Banwell19, Akila Berraf-Tebbal20, V. K. Bhatt, Gregory Bonito21, W. Botha, Treena I. Burgess22, Miroslav Caboň23, J. Calvert24, Lilia C. Carvalhais24, R. Courtecuisse25, P. Cullington, N. Davoodian26, Cony Decock27, Roumen Dimitrov28, S. Di Piazza29, Andre Drenth24, S. Dumez25, Aleš Eichmeier20, Javier Etayo, I. Fernández, J. P. Fiard30, Jacques Fournier, S. Fuentes-Aponte31, M. A.T. Ghanbary32, G. Ghorbani33, A. Giraldo34, A. M. Glushakova14, D.E. Gouliamova28, Josep Guarro7, Francois Halleen35, F. Hampe, Margarita Hernández-Restrepo, I. Iturrieta-González7, Mikael Jeppson2, Aleksey V. Kachalkin14, O. Karimi32, Abdul Nasir Khalid36, A. Khonsanit9, J. I. Kim37, K. Kim31, Munazza Kiran36, Irmgard Krisai-Greilhuber38, Viktor Kučera23, I. Kusan, S. D. Langenhoven35, Teresa Lebel, R. Lebeuf, Kare Liimatainen26, Celeste C. Linde39, Daniel L. Lindner, Lorenzo Lombard, A. E. Mahamedi40, Neven Matočec, Aaron Maxwell, Tom W. May26, Alistair R. McTaggart24, M. Meijer, Armin Mešić, A. J. Mileto12, Andrew N. Miller41, A. Molia, Suchada Mongkolsamrit9, C. Muñoz Cortés16, Justo M. Muñoz-Mohedano17, Asunción Morte17, O.V. Morozova42, Lizel Mostert35, Reza Mostowfizadeh-Ghalamfarsa43, László Nagy, Alfonso Navarro-Ródenas17, L. Örstadius, B. E. Overton12, Viktor Papp44, R. Para, Ursula Peintner45, T. H.G. Pham, Adel Pordel, A. Pošta, A. Rodríguez17, M. K. Romberg31, Marcelo Sandoval-Denis, K. A. Seifert46, K. A. Seifert18, K. C. Semwal47, Brent J. Sewall48, Roger G. Shivas24, M. Slovák23, M. Slovák49, K. Smith, Milan Špetík20, Chris F.J. Spies35, K. Syme26, K. Tasanathai9, R.G. Thorn19, Zdenko Tkalčec, M. A. Tomashevskaya, D. Torres-Garcia7, Z. Ullah36, Cobus M. Visagie1, A. Voitk, L. M. Winton50, Johannes Z. Groenewald 
University of Pretoria1, University of Gothenburg2, Rafael Advanced Defense Systems3, University of Southern Queensland4, Eötvös Loránd University5, University of Turin6, Rovira i Virgili University7, New York Botanical Garden8, Biotec9, University of Tennessee10, Binghamton University11, Lock Haven University of Pennsylvania12, University of Nebraska–Lincoln13, Moscow State University14, Azarbaijan Shahid Madani University15, University of Chile16, University of Murcia17, Agriculture and Agri-Food Canada18, University of Western Ontario19, Mendel University20, Michigan State University21, Murdoch University22, Slovak Academy of Sciences23, University of Queensland24, Lille University of Science and Technology25, Royal Botanic Gardens26, Université catholique de Louvain27, Bulgarian Academy of Sciences28, University of Genoa29, Residence Inn by Marriott30, United States Department of Agriculture31, Sari Agricultural Sciences and Natural Resources University32, University of Maryland College of Agriculture and Natural Resources33, Radboud University Nijmegen34, Stellenbosch University35, University of the Punjab36, Dalhousie University37, University of Vienna38, Australian National University39, École Normale Supérieure40, University of Illinois at Urbana–Champaign41, Russian Academy of Sciences42, Shiraz University43, Szent István University44, University of Innsbruck45, Carleton University46, Eritrea Institute of Technology47, Temple University48, Charles University in Prague49, United States Forest Service50
TL;DR: Novel species of fungi described in this study include those from various countries as follows: Australia, Austroboletus asper on soil, Cylindromonium alloxyli on leaves of Alloxylon pinnatum, Davidhawksworthia quintiniae on Leaves of Quintinia sieberi, Lactifluus lactiglaucus on soil and Neocalonectria tristaniopsidis on leaves.
Abstract: Novel species of fungi described in this study include those from various countries as follows: Australia, Austroboletus asper on soil, Cylindromonium alloxyli on leaves of Alloxylon pinnatum, Davidhawksworthia quintiniae on leaves of Quintinia sieberi, Exophiala prostantherae on leaves of Prostanthera sp., Lactifluus lactiglaucus on soil, Linteromyces quintiniae (incl. Linteromyces gen. nov.) on leaves of Quintinia sieberi, Lophotrichus medusoides from stem tissue of Citrus garrawayi, Mycena pulchra on soil, Neocalonectria tristaniopsidis (incl. Neocalonectria gen. nov.)and Xyladictyochaeta tristaniopsidis on leaves of Tristaniopsis collina, Parasarocladium tasmanniae on leaves of Tasmannia insipida, Phytophthora aquae-cooljarloo from pond water, Serendipita whamiae as endophyte from roots of Eriochilus cucullatus, Veloboletus limbatus (incl. Veloboletus gen. nov.)onsoil. Austria, Cortinarius glaucoelotus onsoil. Bulgaria, Suhomyces rilaensis from the gut of Bolitophagus interruptus found on a Polyporus sp. Canada, Cantharellus betularum among leaf litter of Betula, Penicillium saanichii from house dust. Chile, Circinella lampensis on soil, Exophiala embothrii from rhizosphere of Embothrium coccineum. China, Colletotrichum cycadis on leaves of Cycas revoluta. Croatia, Phialocephala melitaea on fallen branch of Pinus halepensis. Czech Republic, Geoglossum jirinae on soil, Pyrenochaetopsis rajhradensis from dead wood of Buxus sempervirens. Dominican Republic, Amanita domingensis on litter of deciduous wood, Melanoleuca dominicana on forest litter. France, Crinipellis nigrolamellata (Martinique) on leaves of Pisonia fragrans, Talaromyces pulveris from bore dust of Xestobium rufovillosum infesting floorboards. French Guiana, Hypoxylon hepaticolor on dead corticated branch. Great Britain, Inocybe ionolepis on soil. India, Cortinarius indopurpurascens among leaf litter of Quercus leucotrichophora. Iran, Pseudopyricularia javanii on infected leaves of Cyperus sp., Xenomonodictys iranica (incl. Xenomonodictys gen. nov.) on wood of Fagus orientalis. Italy, Penicillium vallebormidaense from compost. Namibia, Alternaria mirabibensis on plant litter, Curvularia moringae and Moringomyces phantasmae (incl. Moringomyces gen. nov.) on leaves and flowers of Moringa ovalifolia, Gobabebomyces vachelliae (incl. Gobabebomyces gen. nov.) on leaves of Vachellia erioloba, Preussia procaviae on dung of Procavia capensis. Pakistan, Russula shawarensis from soil on forest floor. Russia, Cyberlindnera dauci from Daucus carota. South Africa, Acremonium behniae on leaves of Behnia reticulata, Dothiora aloidendri and Hantamomyces aloidendri (incl. Hantamomyces gen. nov.) on leaves of Aloidendron dichotomum, Endoconidioma euphorbiae on leaves of Euphorbia mauritanica , Eucasphaeria proteae on leaves of Protea neriifolia , Exophiala mali from inner fruit tissue of Malus sp., Graminopassalora geissorhizae on leaves of Geissorhiza splendidissima, Neocamarosporium leipoldtiae on leaves of Leipoldtia schultzii, Neocladosporium osteospermi on leaf spots of Osteospermum moniliferum, Neometulocladosporiella seifertii on leaves of Combretum caffrum, Paramyrothecium pituitipietianum on stems of Grielum humifusum, Phytopythium paucipapillatum from roots of Vitis sp., Stemphylium carpobroti and Verrucocladosporium carpobroti on leaves of Carpobrotus quadrifolius, Suttonomyces cephalophylli on leaves of Cephalophyllum pilansii. Sweden, Coprinopsis rubra on cow dung, Elaphomyces nemoreus fromdeciduouswoodlands. Spain, Polyscytalum pini-canariensis on needles of Pinus canariensis, Pseudosubramaniomyces septatus from stream sediment, Tuber lusitanicum on soil under Quercus suber. Thailand, Tolypocladium flavonigrum on Elaphomyces sp. USA, Chaetothyrina spondiadis on fruits of Spondias mombin, Gymnascella minnisii from bat guano, Juncomyces patwiniorum on culms of Juncus effusus, Moelleriella puertoricoensis on scale insect, Neodothiora populina (incl. Neodothiora gen. nov.) on stem cankers of Populus tremuloides, Pseudogymnoascus palmeri fromcavesediment. Vietnam, Cyphellophora vietnamensis on leaf litter, Tylopilus subotsuensis on soil in montane evergreen broadleaf forest. Morphological and culture characteristics are supported by DNA barcodes.

43 citations


Journal ArticleDOI
TL;DR: Mycorrhizal fungi can be isolated from related common species to propagate threatenedCaladenia and using related Caladenia species to infer the presence of suitable fungal OTUs may be feasible.

17 citations


Journal ArticleDOI
TL;DR: Phylogenetic analysis of the ITS region and multilocus concatenation demonstrated that S. avenae is nested within Rhynchosporium, closely related to R. orthosporum and R. lolii.
Abstract: Spermospora avenae causes the economically important red leather leaf disease of oats, which reduces grain yield and hay quality. It was first reported in the USA in 1936 and subsequently in Australia in 1978. Despite this, its phylogenetic placement is unknown, attributed merely to Ascomycota. Twenty-three S. avenae single spore isolates were obtained from affected crops in South Australia and western Victoria from 2008 to 2016. DNA was extracted from each and sequenced using Illumina technology. To identify its closest relatives, a draft genome was de novo assembled and contigs with the highest depth, hypothesised to be the rRNA gene region, were compared to NCBI using the BLASTN function. Contigs that had homologous sequence to the rRNA gene region were used to identify closely related species, which turned out to be Rhynchosporium species. Sequence data from the α-tubulin, β-tubulin, and ITS gene regions of Rhynchosporium species, identified as phylogenetically informative for this genus, were mapped to the S. avenae contigs. Phylogenetic analysis of the ITS region and multilocus concatenation demonstrated that S. avenae is nested within Rhynchosporium, closely related to R. orthosporum and R. lolii. When ITS sequences from other related genera sourced from GenBank were added to the analysis, it appears that Rhynchosporium is paraphyletic and should be split into two genera. Culturally, S. avenae prefers a semi-solid low nutrient medium (ie. ¼ strength PDA made with 1.25% agar) and cool temperature (optimum 15 °C). This corresponds well with the cold wet seasonal conditions required for disease development in the field.

2 citations


Journal ArticleDOI
TL;DR: Despite the large variation observed for Rhynchosporium conidial dimensions, the phylogenetic analyses of the ITS region and concatenated ITS and TUBB loci revealed that all isolates from wild grasses in Iran belong to R. commune, suggesting the potential of the uncultivated grasses as inoculum sources for cultivated barley epidemics and pathogen evolution.
Abstract: There are five described Rhynchosporium species, Rhynchosporium commune, R. secalis, R. agropyri, R. orthosporum and R. lolii, that cause scald diseases on Poaceae. This study used morphological (conidial shape and size) and phylogenetic analyses of two loci (the internal transcribed spacer region (ITS) and β-tubulin (TUBB)) to identify Rhynchosporium species and their host ranges in Iran. Despite the large variation observed for Rhynchosporium conidial dimensions, the phylogenetic analyses of the ITS region and concatenated ITS and TUBB loci revealed that all isolates from wild grasses in Iran belong to R. commune. R. commune was isolated from Hordeum murinum ssp. glaucum, Hordeum vulgare ssp. spontaneum, Lolium multiflorum and Avena sativa in Iran. A. sativa has only been reported from Iran as a host for R. commune. After cross inoculation, A. sativa was considered as the most resistant host showing the lowest susceptibility to R. commune isolates. Of the grass hosts tested, H. vulgare ssp. spontaneum was the most susceptible. The most aggressive isolate across all tested hosts was isolated from Hordeum murinum ssp. glaucum. Cross-infection of the R. commune isolates from all hosts onto uncultivated grasses and cultivated barley suggests the potential of the uncultivated grasses as inoculum sources for cultivated barley epidemics and pathogen evolution. Thus, management of uncultivated grasses in the vicinity of barley fields should assist in managing the disease on cultivated barley.

1 citations