Phylogeny and Morphology of Anthracoidea Pamiroalaica Sp
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Revisiting the Concept of Host Range of Plant Pathogens
PY57CH04_Morris ARjats.cls July 18, 2019 12:43 Annual Review of Phytopathology Revisiting the Concept of Host Range of Plant Pathogens Cindy E. Morris and Benoît Moury Pathologie Végétale, INRA, 84140, Montfavet, France; email: [email protected] Annu. Rev. Phytopathol. 2019. 57:63–90 Keywords First published as a Review in Advance on evolutionary history, network analysis, cophylogeny, host jump, host May 13, 2019 specialization, generalism The Annual Review of Phytopathology is online at phyto.annualreviews.org Abstract https://doi.org/10.1146/annurev-phyto-082718- Strategies to manage plant disease—from use of resistant varieties to crop 100034 rotation, elimination of reservoirs, landscape planning, surveillance, quar- Annu. Rev. Phytopathol. 2019.57:63-90. Downloaded from www.annualreviews.org Copyright © 2019 by Annual Reviews. antine, risk modeling, and anticipation of disease emergences—all rely on All rights reserved knowledge of pathogen host range. However, awareness of the multitude of Access provided by b-on: Universidade de Lisboa (ULisboa) on 09/02/19. For personal use only. factors that influence the outcome of plant–microorganism interactions, the spatial and temporal dynamics of these factors, and the diversity of any given pathogen makes it increasingly challenging to define simple, all-purpose rules to circumscribe the host range of a pathogen. For bacteria, fungi, oomycetes, and viruses, we illustrate that host range is often an overlapping continuum—more so than the separation of discrete pathotypes—and that host jumps are common. By setting the mechanisms of plant–pathogen in- teractions into the scales of contemporary land use and Earth history, we propose a framework to assess the frontiers of host range for practical appli- cations and research on pathogen evolution. -
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. -
Two New Species of Anthracoidea (Ustilaginales) on Carex from North America
MYCOLOGIA BALCANICA 7: 105–109 (2010) 105 Two new species of Anthracoidea (Ustilaginales) on Carex from North America Kálmán Vánky ¹* & Vanamo Salo ² ¹ Herbarium Ustilaginales Vánky (H.U.V.), Gabriel-Biel-Str. 5, D-72076 Tübingen, Germany ² Botanic Garden and Museum, Finnish Museum of Natural History, P.O. Box 7, FI-00014 University of Helsinki, Finland Received 28 November 2010 / Accepted 16 December 2010 Abstract. After a short revision of the genus Anthracoidea, two new species, A. multicaulis on C. geyeri and C. multicaulis, and A. praegracilis on C. praegracilis are described and illustrated. Key words: Anthracoidea, Anthracoidea multicaulis, Anthracoidea praegracilis, Carex, North America, smut fungi, Ustilaginales Introduction Materials and methods Th e genus Anthracoidea Bref. is a natural group in the Th e specimens of Anthracoidea, examined in this study are Anthracoideaceae (Denchev 1997) of the order Ustilaginales, listed in Table 1 and Table 2. parasitising members of Cyperaceae in Carex, Carpha, Fuirena, Sorus and spore characteristics were studied using dried Kobresia, Schoenus, Trichophorum and Uncinia (comp. Vánky herbarium specimens. Spores were dispersed in a droplet 2002: 28–29). Sori around the ovaries as black, globoid, of lactophenol on a microscope slide, covered with a agglutinated spore masses with powdery surface. Spores single, cover glass, gently heated to boiling point to rehydrate the pigmented (dark brown), usually ornamented with spines, spores, and examined by a light microscope (LM) at 1000x warts or granules, rarely smooth, often with internal swellings magnifi cation. For scanning electron microscopy (SEM), dry or light-refractive areas. Spore germination results in two- spores were placed on double-sided adhesive tape, mounted celled basidia forming one or more basidiospores on each cell on a specimen stub, sputter-coated with gold-palladium, ca (Kukkonen 1963, 1964). -
The IUCN Red List of Threatened Speciestm
Species 2014 Annual ReportSpecies the Species of 2014 Survival Commission and the Global Species Programme Species ISSUE 56 2014 Annual Report of the Species Survival Commission and the Global Species Programme • 2014 Spotlight on High-level Interventions IUCN SSC • IUCN Red List at 50 • Specialist Group Reports Ethiopian Wolf (Canis simensis), Endangered. © Martin Harvey Muhammad Yazid Muhammad © Amazing Species: Bleeding Toad The Bleeding Toad, Leptophryne cruentata, is listed as Critically Endangered on The IUCN Red List of Threatened SpeciesTM. It is endemic to West Java, Indonesia, specifically around Mount Gede, Mount Pangaro and south of Sukabumi. The Bleeding Toad’s scientific name, cruentata, is from the Latin word meaning “bleeding” because of the frog’s overall reddish-purple appearance and blood-red and yellow marbling on its back. Geographical range The population declined drastically after the eruption of Mount Galunggung in 1987. It is Knowledge believed that other declining factors may be habitat alteration, loss, and fragmentation. Experts Although the lethal chytrid fungus, responsible for devastating declines (and possible Get Involved extinctions) in amphibian populations globally, has not been recorded in this area, the sudden decline in a creekside population is reminiscent of declines in similar amphibian species due to the presence of this pathogen. Only one individual Bleeding Toad was sighted from 1990 to 2003. Part of the range of Bleeding Toad is located in Gunung Gede Pangrango National Park. Future conservation actions should include population surveys and possible captive breeding plans. The production of the IUCN Red List of Threatened Species™ is made possible through the IUCN Red List Partnership. -
Central European Vegetation
Plant Formations in the Central European BioProvince Peter Martin Rhind Central European Beech Woodlands Beech (Fagus sylvatica) woods form the natural climax over much of Central Europe where the soils are relatively dry and can extend well into the uplands in the more southern zones. In the north, however, around Sweden it is confined to the lowlands. Beech woodlands are often open with a poorly developed shrub layer, Characteristic ground layer species may include various helleborines such as Cephalanthera damasonium, C. longifolia and C. rubra and sedges such as Carex alba, whilst in others, grasses like Sesleria caerlea or Melica uniflora may predominate, but in some of the more acidic examples, Luzula luzuloides is likely to dominate. There are also a number of endemic ground layer species. For example, in Carpathian beech woods endemics such as Dentaria glandulosa (Brassicaceae), Symphytum cordata (Boraginaceae) and the fern Polystichum braunii (Dryopteridaceae) may be encountered. Fine examples of primeaval beech woods can be found in the limestone Alps of lower Austria including the famous ‘Rothwald’ on the southeastern slopes of Dürrentein near Lunz. These range in altitude from about 940-1480 m. Here the canopy is dominated by Fagus sylvatica together with Acer pseudoplatanus, Picea abies, Ulmus glabra, and on the more acidic soils by Abies alba. Typical shrubs include Daphne mezereum, Lonicera alpigena and Rubus hirtus. At ground level the herb layer is very rich supporting possibly up to a 100 species of vascular plants. Examples include Adenostyles alliariae, Asplenium viridis, Campanula scheuchzeri, Cardamine trifolia, Cicerbita alpina, Denteria enneaphyllos, Euphorbia amygdaloides, Galium austriacum, Homogyne alpina, Lycopodium annotinum, Mycelis muralis, Paris quadrifolia, Phyteuma spicata, Prenanthes purpurea, Senecio fuchsii, Valeriana tripteris, Veratrum album and the central European endemic Helliborus niger (Ranunculaceae). -
Literaturverzeichnis
Literaturverzeichnis Abaimov, A.P., 2010: Geographical Distribution and Ackerly, D.D., 2009: Evolution, origin and age of Genetics of Siberian Larch Species. In Osawa, A., line ages in the Californian and Mediterranean flo- Zyryanova, O.A., Matsuura, Y., Kajimoto, T. & ras. Journal of Biogeography 36, 1221–1233. Wein, R.W. (eds.), Permafrost Ecosystems. Sibe- Acocks, J.P.H., 1988: Veld Types of South Africa. 3rd rian Larch Forests. Ecological Studies 209, 41–58. Edition. Botanical Research Institute, Pretoria, Abbadie, L., Gignoux, J., Le Roux, X. & Lepage, M. 146 pp. (eds.), 2006: Lamto. Structure, Functioning, and Adam, P., 1990: Saltmarsh Ecology. Cambridge Uni- Dynamics of a Savanna Ecosystem. Ecological Stu- versity Press. Cambridge, 461 pp. dies 179, 415 pp. Adam, P., 1994: Australian Rainforests. Oxford Bio- Abbott, R.J. & Brochmann, C., 2003: History and geography Series No. 6 (Oxford University Press), evolution of the arctic flora: in the footsteps of Eric 308 pp. Hultén. Molecular Ecology 12, 299–313. Adam, P., 1994: Saltmarsh and mangrove. In Groves, Abbott, R.J. & Comes, H.P., 2004: Evolution in the R.H. (ed.), Australian Vegetation. 2nd Edition. Arctic: a phylogeographic analysis of the circu- Cambridge University Press, Melbourne, pp. marctic plant Saxifraga oppositifolia (Purple Saxi- 395–435. frage). New Phytologist 161, 211–224. Adame, M.F., Neil, D., Wright, S.F. & Lovelock, C.E., Abbott, R.J., Chapman, H.M., Crawford, R.M.M. & 2010: Sedimentation within and among mangrove Forbes, D.G., 1995: Molecular diversity and deri- forests along a gradient of geomorphological set- vations of populations of Silene acaulis and Saxi- tings. -
Notes, Outline and Divergence Times of Basidiomycota
Fungal Diversity (2019) 99:105–367 https://doi.org/10.1007/s13225-019-00435-4 (0123456789().,-volV)(0123456789().,- volV) Notes, outline and divergence times of Basidiomycota 1,2,3 1,4 3 5 5 Mao-Qiang He • Rui-Lin Zhao • Kevin D. Hyde • Dominik Begerow • Martin Kemler • 6 7 8,9 10 11 Andrey Yurkov • Eric H. C. McKenzie • Olivier Raspe´ • Makoto Kakishima • Santiago Sa´nchez-Ramı´rez • 12 13 14 15 16 Else C. Vellinga • Roy Halling • Viktor Papp • Ivan V. Zmitrovich • Bart Buyck • 8,9 3 17 18 1 Damien Ertz • Nalin N. Wijayawardene • Bao-Kai Cui • Nathan Schoutteten • Xin-Zhan Liu • 19 1 1,3 1 1 1 Tai-Hui Li • Yi-Jian Yao • Xin-Yu Zhu • An-Qi Liu • Guo-Jie Li • Ming-Zhe Zhang • 1 1 20 21,22 23 Zhi-Lin Ling • Bin Cao • Vladimı´r Antonı´n • Teun Boekhout • Bianca Denise Barbosa da Silva • 18 24 25 26 27 Eske De Crop • Cony Decock • Ba´lint Dima • Arun Kumar Dutta • Jack W. Fell • 28 29 30 31 Jo´ zsef Geml • Masoomeh Ghobad-Nejhad • Admir J. Giachini • Tatiana B. Gibertoni • 32 33,34 17 35 Sergio P. Gorjo´ n • Danny Haelewaters • Shuang-Hui He • Brendan P. Hodkinson • 36 37 38 39 40,41 Egon Horak • Tamotsu Hoshino • Alfredo Justo • Young Woon Lim • Nelson Menolli Jr. • 42 43,44 45 46 47 Armin Mesˇic´ • Jean-Marc Moncalvo • Gregory M. Mueller • La´szlo´ G. Nagy • R. Henrik Nilsson • 48 48 49 2 Machiel Noordeloos • Jorinde Nuytinck • Takamichi Orihara • Cheewangkoon Ratchadawan • 50,51 52 53 Mario Rajchenberg • Alexandre G. -
A Guide to Frequent and Typical Plant Communities of the European Alps
- Alpine Ecology and Environments A guide to frequent and typical plant communities of the European Alps Guide to the virtual excursion in lesson B1 (Alpine plant biodiversity) Peter M. Kammer and Adrian Möhl (illustrations) – Alpine Ecology and Environments B1 – Alpine plant biodiversity Preface This guide provides an overview over the most frequent, widely distributed, and characteristic plant communities of the European Alps; each of them occurring under different growth conditions. It serves as the basic document for the virtual excursion offered in lesson B1 (Alpine plant biodiversity) of the ALPECOLe course. Naturally, the guide can also be helpful for a real excursion in the field! By following the road map, that begins on page 3, you can determine the plant community you are looking at. Communities you have to know for the final test are indicated with bold frames in the road maps. On the portrait sheets you will find a short description of each plant community. Here, the names of communities you should know are underlined. The portrait sheets are structured as follows: • After the English name of the community the corresponding phytosociological units are in- dicated, i.e. the association (Ass.) and/or the alliance (All.). The names of the units follow El- lenberg (1996) and Grabherr & Mucina (1993). • The paragraph “site characteristics” provides information on the altitudinal occurrence of the community, its topographical situation, the types of substrata, specific climate conditions, the duration of snow-cover, as well as on the nature of the soil. Where appropriate, specifications on the agricultural management form are given. • In the section “stand characteristics” the horizontal and vertical structure of the community is described. -
Anthracoidea Transberingiana, a New Smut Species on Carex Pauciflora from Beringia
Phytotaxa 174 (2): 105–110 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2014 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.174.2.5 Anthracoidea transberingiana, a new smut species on Carex pauciflora from Beringia MARCIN PIĄTEK Department of Mycology, W. Szafer Institute of Botany, Polish Academy of Sciences, Lubicz 46, PL-31-512 Kraków, Poland e-mail: [email protected] Abstract The new smut fungus, Anthracoidea transberingiana attacking ovaries of Carex pauciflora, is described and illustrated from Beringia (Alaska and Kamchatka). The new species is compared with Anthracoidea caricis-pauciflorae infecting the same host plant species predominantly in northern Europe, from which it differs in having smaller spores, thinner spore walls, 2–3 weakly visible internal swellings and somewhat less prominent spore ornamentation. Key words: Anthracoideaceae, Cyperaceae, plant pathogens, smut fungi, Ustilaginales Introduction The few-flowered sedge Carex pauciflora Lightfoot (1777: 543) is a circumpolar species, widely distributed in arctic, boreal and montane ecosystems of North America, Europe and Asia where it occurs mostly on the Sphagnum bogs or different kinds of acidic peat soils (Chater 1980, Hultén & Fries 1986, Egorova 1999, Cochrane 2002). In northern Europe, the few-flowered sedge is rarely infected by the ovary smut Anthracoidea caricis-pauciflorae (Lehtola 1940: 127) Kukkonen (1963: 74). This smut species was also reported from two extra-European stations, namely British Colombia in North America (Kukkonen 1963) and Kamchatka in Asia (Karatygin & Azbukina 1989). In the European and world smut monographs, Vánky (1994, 2012) reported that A. caricis-pauciflorae occurs in northern Europe, northern North America and north-east Asia. -
Lepidoptera: Elachistidae) SHILAP Revista De Lepidopterología, Vol
SHILAP Revista de Lepidopterología ISSN: 0300-5267 [email protected] Sociedad Hispano-Luso-Americana de Lepidopterología España Parenti, U.; Pizzolato, F. Revision of European Elachistidae. The genus Biselachista Traugott-Olsen & Nielsen, 1977, stat. rev. (Lepidoptera: Elachistidae) SHILAP Revista de Lepidopterología, vol. 43, núm. 172, diciembre, 2015, pp. 537-559 Sociedad Hispano-Luso-Americana de Lepidopterología Madrid, España Available in: http://www.redalyc.org/articulo.oa?id=45543699003 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative SHILAP Revta. lepid., 43 (172), diciembre 2015: 537-575 eISSN: 2340-4078 ISSN: 0300-5267 Revision of European Elachistidae. The genus Biselachista Traugott-Olsen & Nielsen, 1977, stat. rev. (Lepidoptera: Elachistidae) U. Parenti (†) & F. Pizzolato Abstract The genus Biselachista Traugott-Olsen & Nielsen, 1977, with a Holarctic diffusion and represented in Europe by seventeen species living in various environments, from sea level to 2000 metres in the Alps, is considered a valid genus. The biology of some species is well known thanks to laboratory rearings. Their host plants and parasites are reported. The pre-imaginal stages and the male and female genitalia are illustrated. The currently ascertained distribution is given. The examination of the type material permitted to ascertain the following synonymies: Biselachista occidentalis (Frey, 1882) is a synonym of Biselachista juliensis (Frey, 1870); Elachista saarelai Kaila & Sippola, 2010 is a synonym of Biselachista kebneella Traugott-Olsen & Nielsen, 1977. KEY WORDS: Lepidoptera, Elachistidae, Biselachista, biology, genitalia, distribution, Europe. -
Mykologie Tübingen-15.3.12
Mykologie am Lehrstuhl Spezielle Botanik und Mykologie der Universität Tübingen, 1974-2011 FRANZ OBERWINKLER Kurzfassung Wir beschreiben die mykologischen Forschungsaktivitäten am ehemaligen Lehrstuhl „Spezi- elle Botanik und Mykologie“ der Universität Tübingen von 1974 bis 2011 und ihre interna- tionalen Ausstrahlung. Leitschiene unseres gemeinsamen mykologischen Forschungskonzep- tes war die Verknüpfung von Gelände- mit Laborarbeiten sowie von Forschung mit Lehre. Dieses Konzept spiegelte sich in einem weit gefächerten Lehrangebot, das insbesondere den Pflanzen als dem Hauptsubstrat der Pilze breiten Raum gab. Lichtmikroskopische Untersu- chungen der zellulären Baupläne von Pilzen bildeten das Fundament für unsere Arbeiten: Identifikationen, Ontogeniestudien, Vergleiche von Mikromorphologien, Überprüfen von Kulturen, Präparateauswahl für Elektronenmikroskopie, etc. Bereits an diesen Beispielen wird die Methodenvernetzung erkennbar. In dem zu besprechenden Zeitraum wurden Ultrastrukturuntersuchungen und Nukleinsäurese- quenzierungen als revolutionierende Methoden für den täglichen Laborbetrieb verfügbar. Flankiert wurden diese Neuerungen durch ständig verbesserte Datenaufbereitungen und Aus- wertungsprogramme für Computer. Zusammen mit den traditionellen Anwendungen der Lichtmikroskopie und der Kultivierung von Pilzen stand somit ein effizientes Methodenspek- trum zur Verfügung, das für systematische, phylogenetische und ökologische Fragestellungen gleichermaßen eingesetzt werden konnte, insbesondere in der Antibiotikaforschung, beim -
Phylogeny and Morphology of Anthracoidea Pamiroalaica Sp. Nov
Mycol Progress (2015) 14: 120 DOI 10.1007/s11557-015-1140-1 ORIGINAL ARTICLE Phylogeny and morphology of Anthracoidea pamiroalaica sp. nov. infecting the endemic sedge Carex koshewnikowii in the Pamir Alai Mts (Tajikistan) Marcin Piątek1 & Matthias Lutz2 & Marcin Nobis3 & Arkadiusz Nowak4 Received: 24 July 2015 /Revised: 16 October 2015 /Accepted: 2 November 2015 /Published online: 28 November 2015 # The Author(s) 2015. This article is published with open access at Springerlink.com Abstract AnovelAnthracoidea species, A. pamiroalaica on Introduction the endemic sedge Carex koshewnikowii, is described and illustrated from the Pamir Alai Mts in Tajikistan (Central The genus Anthracoidea Bref., typified by Anthracoidea Asia). The new species is phenotypically nearly identical with caricis (Pers.) Bref., includes smut fungi infecting host plants Anthracoidea sempervirentis, but clearly divergent genetical- in the Cyperaceae (mostly species of Carex L.), forming glo- ly. Phylogenetic analyses based on LSU sequences showed boid sori in the ovaries and having spores produced directly on affinity of Anthracoidea pamiroalaica to A. baldensis, the outer surface of the reduced achenes (Kukkonen 1963; A. rupestris, A. capillaris,andA. vankyi infecting host sedges Vánky 2002). The species delimitation traditionally was based in different Carex sections (Baldenses, Rupestres, on comparative morphology and phenotypic differences be- Chlorostachyae, and Phaestoglochin, respectively), but not tween Anthracoidea species attacking host plants within a to A. misandrae,andA. sempervirentis, two sequenced spe- particular Carex section (Nannfeldt 1979;Vánky1979, cies parasitic on host species from the section Aulocystis.This 2012). The first molecular phylogenetic study using LSU phylogenetic placement is briefly discussed in the context of rDNA sequences including 28 Anthracoidea species (and Anthracoidea evolution.