Snow Molds of Turfgrasses, RPD No
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Abacca Mosaic Virus
Annex Decree of Ministry of Agriculture Number : 51/Permentan/KR.010/9/2015 date : 23 September 2015 Plant Quarantine Pest List A. Plant Quarantine Pest List (KATEGORY A1) I. SERANGGA (INSECTS) NAMA ILMIAH/ SINONIM/ KLASIFIKASI/ NAMA MEDIA DAERAH SEBAR/ UMUM/ GOLONGA INANG/ No PEMBAWA/ GEOGRAPHICAL SCIENTIFIC NAME/ N/ GROUP HOST PATHWAY DISTRIBUTION SYNONIM/ TAXON/ COMMON NAME 1. Acraea acerata Hew.; II Convolvulus arvensis, Ipomoea leaf, stem Africa: Angola, Benin, Lepidoptera: Nymphalidae; aquatica, Ipomoea triloba, Botswana, Burundi, sweet potato butterfly Merremiae bracteata, Cameroon, Congo, DR Congo, Merremia pacifica,Merremia Ethiopia, Ghana, Guinea, peltata, Merremia umbellata, Kenya, Ivory Coast, Liberia, Ipomoea batatas (ubi jalar, Mozambique, Namibia, Nigeria, sweet potato) Rwanda, Sierra Leone, Sudan, Tanzania, Togo. Uganda, Zambia 2. Ac rocinus longimanus II Artocarpus, Artocarpus stem, America: Barbados, Honduras, Linnaeus; Coleoptera: integra, Moraceae, branches, Guyana, Trinidad,Costa Rica, Cerambycidae; Herlequin Broussonetia kazinoki, Ficus litter Mexico, Brazil beetle, jack-tree borer elastica 3. Aetherastis circulata II Hevea brasiliensis (karet, stem, leaf, Asia: India Meyrick; Lepidoptera: rubber tree) seedling Yponomeutidae; bark feeding caterpillar 1 4. Agrilus mali Matsumura; II Malus domestica (apel, apple) buds, stem, Asia: China, Korea DPR (North Coleoptera: Buprestidae; seedling, Korea), Republic of Korea apple borer, apple rhizome (South Korea) buprestid Europe: Russia 5. Agrilus planipennis II Fraxinus americana, -
Major Clades of Agaricales: a Multilocus Phylogenetic Overview
Mycologia, 98(6), 2006, pp. 982–995. # 2006 by The Mycological Society of America, Lawrence, KS 66044-8897 Major clades of Agaricales: a multilocus phylogenetic overview P. Brandon Matheny1 Duur K. Aanen Judd M. Curtis Laboratory of Genetics, Arboretumlaan 4, 6703 BD, Biology Department, Clark University, 950 Main Street, Wageningen, The Netherlands Worcester, Massachusetts, 01610 Matthew DeNitis Vale´rie Hofstetter 127 Harrington Way, Worcester, Massachusetts 01604 Department of Biology, Box 90338, Duke University, Durham, North Carolina 27708 Graciela M. Daniele Instituto Multidisciplinario de Biologı´a Vegetal, M. Catherine Aime CONICET-Universidad Nacional de Co´rdoba, Casilla USDA-ARS, Systematic Botany and Mycology de Correo 495, 5000 Co´rdoba, Argentina Laboratory, Room 304, Building 011A, 10300 Baltimore Avenue, Beltsville, Maryland 20705-2350 Dennis E. Desjardin Department of Biology, San Francisco State University, Jean-Marc Moncalvo San Francisco, California 94132 Centre for Biodiversity and Conservation Biology, Royal Ontario Museum and Department of Botany, University Bradley R. Kropp of Toronto, Toronto, Ontario, M5S 2C6 Canada Department of Biology, Utah State University, Logan, Utah 84322 Zai-Wei Ge Zhu-Liang Yang Lorelei L. Norvell Kunming Institute of Botany, Chinese Academy of Pacific Northwest Mycology Service, 6720 NW Skyline Sciences, Kunming 650204, P.R. China Boulevard, Portland, Oregon 97229-1309 Jason C. Slot Andrew Parker Biology Department, Clark University, 950 Main Street, 127 Raven Way, Metaline Falls, Washington 99153- Worcester, Massachusetts, 01609 9720 Joseph F. Ammirati Else C. Vellinga University of Washington, Biology Department, Box Department of Plant and Microbial Biology, 111 355325, Seattle, Washington 98195 Koshland Hall, University of California, Berkeley, California 94720-3102 Timothy J. -
Biotype Differentiation in the Typhula Ishikariensis Complex and Their Allopatry in Hokkaido
日 植 病 報 48: 275-280 (1982) Ann. Phytopath. Soc. Japan 48: 275-280 (1982) Biotype Differentiation in the Typhula ishikariensis Complex and Their Allopatry in Hokkaido Naoyuki MATSUMOTO*, Toru SATO** and Takao ARAKI*** 松 本 直 幸 *・佐藤 徹 **・荒木 隆 男***:雪腐 黒 色 小 粒 菌 核 病 菌 の生 物 型 と そ れ らの 北 海 道 内 に お け る異 所 性 Abstract Typhula ishikariensis isolates were collected from various parts of Hokkaido. There were two genetically different groups which did not mate with each other; one was termed biotype A, and the other was further divided into two by cultural characteristics, i.e., biotypes B and C. Biotype A was identical to T. ishikariensis and T. ishikariensis var. ishikariensis. Biotype B was not identical to T. idahoensis or T. ishikariensis var. idahoensis. Biotype C was similar to T. ishikariensis var. canadensis. Biotype A tended to occur inland where deep snow cover lasts for a long time. Biotype B was obtained mainly from the coastal regions where snow cover is thin and short in time. The distribution of biotype C was irregular. Taxonomic significance of the genetics and allopatry in the T. ishikari- ensis complex is discussed. (Received August 31, 1981) Key Words: snow mold fungi, taxonomy, distribution. Introduction Pathogenic species of Typhula had been confused in taxonomy until McDonald14) reviewed the literature on these fungi in 1961. Although he suggested the need for the comparison of many specimens from different sources by one investigator, he placed T. ishikariensis S. Imai and T. -
How Many Fungi Make Sclerotia?
fungal ecology xxx (2014) 1e10 available at www.sciencedirect.com ScienceDirect journal homepage: www.elsevier.com/locate/funeco Short Communication How many fungi make sclerotia? Matthew E. SMITHa,*, Terry W. HENKELb, Jeffrey A. ROLLINSa aUniversity of Florida, Department of Plant Pathology, Gainesville, FL 32611-0680, USA bHumboldt State University of Florida, Department of Biological Sciences, Arcata, CA 95521, USA article info abstract Article history: Most fungi produce some type of durable microscopic structure such as a spore that is Received 25 April 2014 important for dispersal and/or survival under adverse conditions, but many species also Revision received 23 July 2014 produce dense aggregations of tissue called sclerotia. These structures help fungi to survive Accepted 28 July 2014 challenging conditions such as freezing, desiccation, microbial attack, or the absence of a Available online - host. During studies of hypogeous fungi we encountered morphologically distinct sclerotia Corresponding editor: in nature that were not linked with a known fungus. These observations suggested that Dr. Jean Lodge many unrelated fungi with diverse trophic modes may form sclerotia, but that these structures have been overlooked. To identify the phylogenetic affiliations and trophic Keywords: modes of sclerotium-forming fungi, we conducted a literature review and sequenced DNA Chemical defense from fresh sclerotium collections. We found that sclerotium-forming fungi are ecologically Ectomycorrhizal diverse and phylogenetically dispersed among 85 genera in 20 orders of Dikarya, suggesting Plant pathogens that the ability to form sclerotia probably evolved 14 different times in fungi. Saprotrophic ª 2014 Elsevier Ltd and The British Mycological Society. All rights reserved. Sclerotium Fungi are among the most diverse lineages of eukaryotes with features such as a hyphal thallus, non-flagellated cells, and an estimated 5.1 million species (Blackwell, 2011). -
Basidiomycota: Agaricales) Introducing the Ant-Associated Genus Myrmecopterula Gen
Leal-Dutra et al. IMA Fungus (2020) 11:2 https://doi.org/10.1186/s43008-019-0022-6 IMA Fungus RESEARCH Open Access Reclassification of Pterulaceae Corner (Basidiomycota: Agaricales) introducing the ant-associated genus Myrmecopterula gen. nov., Phaeopterula Henn. and the corticioid Radulomycetaceae fam. nov. Caio A. Leal-Dutra1,5, Gareth W. Griffith1* , Maria Alice Neves2, David J. McLaughlin3, Esther G. McLaughlin3, Lina A. Clasen1 and Bryn T. M. Dentinger4 Abstract Pterulaceae was formally proposed to group six coralloid and dimitic genera: Actiniceps (=Dimorphocystis), Allantula, Deflexula, Parapterulicium, Pterula, and Pterulicium. Recent molecular studies have shown that some of the characters currently used in Pterulaceae do not distinguish the genera. Actiniceps and Parapterulicium have been removed, and a few other resupinate genera were added to the family. However, none of these studies intended to investigate the relationship between Pterulaceae genera. In this study, we generated 278 sequences from both newly collected and fungarium samples. Phylogenetic analyses supported with morphological data allowed a reclassification of Pterulaceae where we propose the introduction of Myrmecopterula gen. nov. and Radulomycetaceae fam. nov., the reintroduction of Phaeopterula, the synonymisation of Deflexula in Pterulicium, and 53 new combinations. Pterula is rendered polyphyletic requiring a reclassification; thus, it is split into Pterula, Myrmecopterula gen. nov., Pterulicium and Phaeopterula. Deflexula is recovered as paraphyletic alongside several Pterula species and Pterulicium, and is sunk into the latter genus. Phaeopterula is reintroduced to accommodate species with darker basidiomes. The neotropical Myrmecopterula gen. nov. forms a distinct clade adjacent to Pterula, and most members of this clade are associated with active or inactive attine ant nests. -
Minireview Snow Molds: a Group of Fungi That Prevail Under Snow
Microbes Environ. Vol. 24, No. 1, 14–20, 2009 http://wwwsoc.nii.ac.jp/jsme2/ doi:10.1264/jsme2.ME09101 Minireview Snow Molds: A Group of Fungi that Prevail under Snow NAOYUKI MATSUMOTO1* 1Department of Planning and Administration, National Agricultural Research Center for Hokkaido Region, 1 Hitsujigaoka, Toyohira-ku, Sapporo 062–8555, Japan (Received January 5, 2009—Accepted January 30, 2009—Published online February 17, 2009) Snow molds are a group of fungi that attack dormant plants under snow. In this paper, their survival strategies are illustrated with regard to adaptation to the unique environment under snow. Snow molds consist of diverse taxonomic groups and are divided into obligate and facultative fungi. Obligate snow molds exclusively prevail during winter with or without snow, whereas facultative snow molds can thrive even in the growing season of plants. Snow molds grow at low temperatures in habitats where antagonists are practically absent, and host plants deteriorate due to inhibited photosynthesis under snow. These features characterize snow molds as opportunistic parasites. The environment under snow represents a habitat where resources available are limited. There are two contrasting strategies for resource utilization, i.e., individualisms and collectivism. Freeze tolerance is also critical for them to survive freezing temper- atures, and several mechanisms are illustrated. Finally, strategies to cope with annual fluctuations in snow cover are discussed in terms of predictability of the habitat. Key words: snow mold, snow cover, low temperature, Typhula spp., Sclerotinia borealis Introduction Typical snow molds have a distinct life cycle, i.e., an active phase under snow and a dormant phase from spring to In northern regions with prolonged snow cover, plants fall. -
Novel Antifungal Activity of Lolium-Associated Epichloë Endophytes
microorganisms Article Novel Antifungal Activity of Lolium-Associated Epichloë Endophytes Krishni Fernando 1,2, Priyanka Reddy 1, Inoka K. Hettiarachchige 1, German C. Spangenberg 1,2, Simone J. Rochfort 1,2 and Kathryn M. Guthridge 1,* 1 Agriculture Victoria, AgriBio, Centre for AgriBioscience, Bundoora, 3083 Victoria, Australia; [email protected] (K.F.); [email protected] (P.R.); [email protected] (I.K.H.); [email protected] (G.C.S.); [email protected] (S.J.R.) 2 School of Applied Systems Biology, La Trobe University, Bundoora, 3083 Victoria, Australia * Correspondence: [email protected]; Tel.: +61390327062 Received: 27 May 2020; Accepted: 19 June 2020; Published: 24 June 2020 Abstract: Asexual Epichloë spp. fungal endophytes have been extensively studied for their functional secondary metabolite production. Historically, research mostly focused on understanding toxicity of endophyte-derived compounds on grazing livestock. However, endophyte-derived compounds also provide protection against invertebrate pests, disease, and other environmental stresses, which is important for ensuring yield and persistence of pastures. A preliminary screen of 30 strains using an in vitro dual culture bioassay identified 18 endophyte strains with antifungal activity. The novel strains NEA12, NEA21, and NEA23 were selected for further investigation as they are also known to produce alkaloids associated with protection against insect pests. Antifungal activity of selected endophyte strains was confirmed against three grass pathogens, Ceratobasidium sp., Dreschlera sp., and Fusarium sp., using independent isolates in an in vitro bioassay. NEA21 and NEA23 showed potent activity against Ceratobasidium sp. -
Turfgrass Pest Management
MSUE Pesticide Education Program TurfgrassTurfgrass PestPest ManagementManagement TrainingTraining forfor CommercialCommercial PesticidePesticide ApplicatorsApplicators Category 3A Developed by Greg Patchan, Julie Stachecki, and Kay Sicheneder MSUE Pesticide Education Program PrinciplesPrinciples ofof PestPest ManagementManagement Chapter 1 A pesticide applicator doesn’t just apply pesticides. Social and legal responsibilities accompany the use of toxic materials. MSUE Pesticide Education Program Pesticide application must protect plant material from pest injury without endangering nontarget organisms. MSUE Pesticide Education Program Integrated Pest Management MSUE Pesticide Education Program IPMIPM n Use of all available strategies to manage pests. n Achieve acceptable yield and quality. n Least environmental disruption. MSUE Pesticide Education Program IPMIPM PestPest ControlControl StrategiesStrategies n Resistant varieties n Cultural practices n Natural enemies n Mechanical controls n Pesticides n IPM is NOT anti-pesticide IPMIPM waswas developeddeveloped forfor agricultureagriculture because....because.... n No one method achieves long term pest management. n Pest management is a part of plant care. n Reduce costs. n Failures, resistance, pollution were the lessons. MSUE Pesticide Education Program IPMIPM StepsSteps forfor TurfgrassTurfgrass n Detection of what is injuring turfgrass. n Identification of agents injuring turfgrass. n Economic significance. n Selection of methods. n Evaluation. MSUE Pesticide Education Program Detection-MonitoringDetection-Monitoring -
Bibliografía Botánica Ibérica, 2010 Fungi
Botanica Complutensis 35: 177-182. 2011 ISSN: 0214-4565 Bibliografía Botánica Ibérica, 2010 Fungi Ana Rosa Burgaz1 2044. ALVARADO, P.; MANJÓN, J. L.; MATHENY, P. B. & ESTEVE- en la depresión del Guadalquivir (Granada). Lactarius RAVENTÓS, F. 2010. Tubariomyces, a new genus of Inocy- 18: 19-27. (Tax, Montagnea, Gr). baceae from the Mediterranean region. Mycologia 2054. BOTELLA, L.; SANTAMARÍA, O. & DÍEZ, J. J. 2010. Fun- 102(69): 1389-1397. (SisM, Tubariomyces, Bu, To, Vi). gi associated with the decline of Pinus halepensis in 2045. ARRILLAGA ANABITARTE, P. & MAYO Z ECHANIZ, M. I. Spain. Fungal Diversity 40: 1-11. (Fitopat, Ascomyce- 2006. Los hongos alucinógenos en la cultura de los pue- tes, A, B, Cu, Ge, Gr, L, M, Ma, Mu, T, Te, V, Z). blos. Aranzadiana 127: 232-243. (Etnobot, Ascomyce- 2055, BURGAZ, A. R. 2010. Bibliografía Botánica Ibérica, tes, Basidiomycetes). 2009. Bot. Complut. 34: 101-111. (Bibl). 2046. AZCÓN-AGUILAR, C.; PALENZUELA JIMÉNEZ, J.; RUIZ GI- 2056. CADIÑANOS-AGUIRRE, J. A. & MATEOS-IZQUIERDO, A. RELA, M.; FERROL, N.; AZCÓN, R.; IRURITA, J. M. & BA- 2010. El complejo Cortinarius cedretorum-C. elegan- REA NAVARRO, J. M. 2010. Análisis de la diversidad de tissimus en España. Bol. Soc. Micol. Madrid 34: 73- micorrizas y hongos micorrícicos asociados a especies 85. (Tax, Ecol, Cortinarius, B, Ba, Bi, Bu, Cc, Cs, Hu, de flora amenazada del Parque Nacional de Sierra Ne- S, Vi). vada: 173-190. En: L. Ramírez & B. Asensio (Eds.), Pro- 2057. CALONGE, F. D. 2010. Lepiota brunneoincarnata: se- yectos de Investigación en Parques Nacionales: 2006- gundo caso de envenenamiento familiar grave en Ma- 2009. -
Typhula Blight Paul Koch, UW-Plant Pathology and PJ Liesch, UW Insect Diagnostic Lab
XHT1270 Provided to you by: Typhula Blight Paul Koch, UW-Plant Pathology and PJ Liesch, UW Insect Diagnostic Lab What is Typhula blight? Typhula blight, also known as gray or speckled snow mold, is a fungal disease affecting all cool season turf grasses (e.g., Kentucky bluegrass, creeping bentgrass, tall fescue, fine fescue, perennial ryegrass) grown in areas with prolonged snow cover. These grasses are widely used in residential lawns and golf courses in Wisconsin and elsewhere in the Midwest. What does Typhula blight look like? Typhula blight initially appears as roughly circular patches of bleached or straw-colored turf that can be up to two to three feet in diameter. When the disease is severe, patches can merge to form larger, irregularly-shaped bleached areas. Affected turf is often matted and can have a water-soaked appearance. At the edges of patches, masses of grayish-white fungal threads (called a mycelium) may form. In 1 3 addition, tiny ( /64 to /16 inch diameter) reddish-brown or black fungal survival Typhula blight causes circular patches of structures (called sclerotia) may be bleached turf that often merge to form larger, irregularly-shaped bleached areas. present. Typhula blight looks very similar to Microdochium patch/pink snow mold (see University of Wisconsin Garden Facts XHT1145, Microdochium Patch), but the Microdochium patch fungus does not produce sclerotia. Where does Typhula blight come from? Typhula blight is caused by two closely related fungi Typhula incarnata and Typhula ishikariensis. In general, T. incarnata is more common in the southern half of Wisconsin while T. ishikariensis is more common in the northern half of the state. -
Genetic and Pathogenic Differences Between Microdochium Nivale and Microdochium Majus
Genetic and Pathogenic Differences Between Microdochium nivale and Microdochium majus by Linda Elizabeth Jewell A Thesis Presented to The University of Guelph In partial fulfilment of requirements for the degree of Doctor of Philosophy in Environmental Science Guelph, Ontario, Canada © Linda Elizabeth Jewell, December, 2013 ABSTRACT GENETIC AND PATHOGENIC DIFFERENCES BETWEEN MICRODOCHIUM NIVALE AND MICRODOCHIUM MAJUS Linda Elizabeth Jewell Advisor: University of Guelph, 2013 Professor Tom Hsiang Microdochium nivale and M. majus are fungal plant pathogens that cause cool-temperature diseases on grasses and cereals. Nucleotide sequences of four genetic regions were compared between isolates of M. nivale and M. majus from Triticum aestivum (wheat) collected in North America and Europe and for isolates of M. nivale from turfgrasses from both continents. Draft genome sequences were assembled for two isolates of M. majus and two of M. nivale from wheat and one from turfgrass. Dendograms constructed from these data resolved isolates of M. majus into separate clades by geographic origin. Among M. nivale, isolates were instead resolved by host plant species. Amplification of repetitive regions of DNA from M. nivale isolates collected from two proximate locations across three years grouped isolates by year, rather than by location. The mating-type (MAT1) and associated flanking genes of Microdochium were identified using the genome sequencing data to investigate the potential for these pathogens to produce ascospores. In all of the Microdochium genomes, and in all isolates assessed by PCR, only the MAT1-2-1 gene was identified. However, unpaired, single-conidium-derived colonies of M. majus produced fertile perithecia in the lab. -
Basidiomycetous Yeast, Glaciozyma Antarctica, Forming Frost-Columnar Colonies on Frozen Medium
microorganisms Article Basidiomycetous Yeast, Glaciozyma antarctica, Forming Frost-Columnar Colonies on Frozen Medium Seiichi Fujiu 1,2,3, Masanobu Ito 1,3, Eriko Kobayashi 1,3, Yuichi Hanada 1,2, Midori Yoshida 4, Sakae Kudoh 5,* and Tamotsu Hoshino 1,6,* 1 Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), 2-17-2-1, Tsukisamu-higashi, Toyohira-ku, Sapporo 062-8517, Hokkaido, Japan; [email protected] (S.F.); [email protected] (M.I.); [email protected] (E.K.); [email protected] (Y.H.) 2 Graduate School of Science, Hokkaido University, N10 W8, Kita-ku, Sapporo 060-0810, Hokkaido, Japan 3 School of Biological Sciences, Tokai University, 1-1-1, Minaminosawa 5, Minami-ku, Sapporo 005-0825, Hokkaido, Japan 4 Hokkaido Agricultural Research Center, NARO, Hitsujigaoka 1, Toyohira-ku, Sapporo 062-8555, Hokkaido, Japan; [email protected] 5 Biology Group, National Institute of Polar Research, 10-3, Midori-cho, Tachikawa, Tokyo 190-8518, Japan 6 Department of Life and Environmental Science, Faculty of Engineering, Hachinohe Institute of Technology, Obiraki 88-1, Myo, Hachinohe 031-8501, Aomori, Japan * Correspondence: [email protected] (S.K.); [email protected] (T.H.); Tel.: +81-42-512-0739 (S.K.); +81-178-25-8174 (T.H.); Fax: +81-42-528-3492 (S.K.); +81-178-25-6825 (T.H.) Abstract: The basidiomycetous yeast, Glaciozyma antarctica, was isolated from various terrestrial materials collected from the Sôya coast, East Antarctica, and formed frost-columnar colonies on agar plates frozen at −1 ◦C.