The Divorce of Sporothrix and Ophiostoma: Solution to a Problematic Relationship
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												Method to Estimate Dry-Kiln Schedules and Species Groupings: Tropical and Temperate Hardwoods
United States Department of Agriculture Method to Estimate Forest Service Forest Dry-Kiln Schedules Products Laboratory Research and Species Groupings Paper FPL–RP–548 Tropical and Temperate Hardwoods William T. Simpson Abstract Contents Dry-kiln schedules have been developed for many wood Page species. However, one problem is that many, especially tropical species, have no recommended schedule. Another Introduction................................................................1 problem in drying tropical species is the lack of a way to Estimation of Kiln Schedules.........................................1 group them when it is impractical to fill a kiln with a single Background .............................................................1 species. This report investigates the possibility of estimating kiln schedules and grouping species for drying using basic Related Research...................................................1 specific gravity as the primary variable for prediction and grouping. In this study, kiln schedules were estimated by Current Kiln Schedules ..........................................1 establishing least squares relationships between schedule Method of Schedule Estimation...................................2 parameters and basic specific gravity. These relationships were then applied to estimate schedules for 3,237 species Estimation of Initial Conditions ..............................2 from Africa, Asia and Oceana, and Latin America. Nine drying groups were established, based on intervals of specific Estimation - 
												
												The Flora Protection Act, 2000 Legal Notice No.10 of 2000
The Flora Protection Act, 2000 Legal Notice No.10 of 2000 Gazetted as VOL. XXXVI I I MBABANE, Friday, Septem ber 22nd., 2000 [ No. 606] Presented by the Minister for Agriculture and Cooperatives MEMORANDUM OF OBJECTS AND REASONS The purpose of this Bill is to repeal and replace the Flora Protection Act No. 45 of 1952 so as to provide for m ore effective protection of flora and to provide for m atters incidental thereto. P. M. DLAMI NI Attorney General A BI LL entitled An Act to protect indigenous flora and to provide for m atters incidental thereto. ENACTED by the King and the Parliam ent of Swaziland. Short title and commencement 1. This Act m ay be cited as the Flora Protection Act, 2000 and shall com e into force on such date as the Minister m ay, by notice in the Gazette, appoint. Interpretation 2. I n this Act, unless the context otherwise requires: - "Authority" m eans the Swaziland Environm ent Authority established by the Swaziland Environm ent Authority Act No. 15 of 1992; "cultivate" m eans to prom ote, stim ulate or foster the growth of a plant, or plant m aterial (including seed) obtained lawfully in term s of this Act, and "cultivated" and "cultivation" have corresponding m eanings; "endem ic flora" m eans any flora whose natural distribution is restricted to the boundaries of Swaziland; "flora reserve" m eans a reserve established in term s of Section 3; "indigenous flora" m eans any plant whose natural distribution is Southern Africa including Swaziland; "land" includes land with or without buildings thereon; "Minister" m eans the Minister responsible for Flora; "plant" m eans any vegetative or reproductive growth including fungi, algae, m osses, lichens, liverworts, ferns, fern allies or seed plant whether living or dead; "owner" m eans: - a. - 
												
												Microsatellite and Mating Type Markers Reveal Unexpected Patterns of Genetic Diversity in the Pine Root-Infecting Fungus Grosmannia Alacris
Plant Pathology (2015) 64, 235–242 Doi: 10.1111/ppa.12231 Microsatellite and mating type markers reveal unexpected patterns of genetic diversity in the pine root-infecting fungus Grosmannia alacris T. A. Duonga*, Z. W. de Beerb, B. D. Wingfielda, L. G. Eckhardtc and M. J. Wingfielda aDepartment of Genetics, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria 0002, South Africa; bDepartment of Microbiology and Plant Pathology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria 0002, South Africa; and cForest Health Dynamics Laboratory, School of Forestry and Wildlife Sciences, Auburn University, Auburn, AL 36849, USA Grosmannia alacris is a fungus commonly associated with root-infesting bark beetles occurring on Pinus spp. The fun- gus has been recorded in South Africa, the USA, France, Portugal and Spain and importantly, has been associated with pine root diseases in South Africa and the USA. Nothing is known regarding the population genetics or origin of G. alacris, although its association with root-infesting beetles native to Europe suggests that it is an invasive alien in South Africa. In this study, microsatellite markers together with newly developed mating type markers were used to characterize a total of 170 isolates of G. alacris from South Africa and the USA. The results showed that the genotypic diversity of the South African population of G. alacris was very high when compared to the USA populations. Two mating types were also present in South African isolates and the MAT1-1/MAT1-2 ratio did not differ from 1:1 (v2 = 1Á39, P = 0Á24). This suggests that sexual reproduction most probably occurs in the fungus in South Africa, although a sexual state has never been seen in nature. - 
												
												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. - 
												
												Developments in Fungal Taxonomy
CLINICAL MICROBIOLOGY REVIEWS, July 1999, p. 454–500 Vol. 12, No. 3 0893-8512/99/$04.00ϩ0 Copyright © 1999, American Society for Microbiology. All Rights Reserved. Developments in Fungal Taxonomy JOSEP GUARRO,* JOSEPA GENE´, AND ALBERTO M. STCHIGEL Unitat de Microbiologia, Departament de Cie`ncies Me`diques Ba`siques, Facultat de Medicina i Cie`ncies de la Salut, Universitat Rovira i Virgili, 43201 Reus, Spain INTRODUCTION .......................................................................................................................................................454 THE CONCEPT OF SPECIES IN FUNGI .............................................................................................................455 PHYLOGENY AND EVOLUTION...........................................................................................................................455 NOMENCLATURE.....................................................................................................................................................456 CURRENT MYCOLOGICAL TYPING METHODS..............................................................................................457 Morphology..............................................................................................................................................................457 Downloaded from Molecular Techniques ............................................................................................................................................459 Other Techniques....................................................................................................................................................460 - 
												
												Multi-Gene Phylogenies Define Ceratocystiopsis and Grosmannia
STUDIES IN MYCOLOGY 55: 75–97. 2006. Multi-gene phylogenies define Ceratocystiopsis and Grosmannia distinct from Ophiostoma Renate D. Zipfel1, Z. Wilhelm de Beer2*, Karin Jacobs3, Brenda D. Wingfield1 and Michael J. Wingfield2 1Department of Genetics, 2Department of Microbiology and Plant Pathology, Forestry and Agricultural Biotechnology Institute (FABI), University of Pretoria, Pretoria, 0002, South Africa; 3Department of Microbiology, University of Stellenbosch, Private Bag X1, Matieland, Stellenbosch, South Africa *Correspondence: Z. Wilhelm de Beer, [email protected] Abstract: Ophiostoma species have diverse morphological features and are found in a large variety of ecological niches. Many different classification schemes have been applied to these fungi in the past based on teleomorph and anamorph features. More recently, studies based on DNA sequence comparisions have shown that Ophiostoma consists of different phylogenetic groups, but the data have not been sufficient to define clear monophyletic lineages represented by practical taxonomic units. We used DNA sequence data from combined partial nuclear LSU and β-tubulin genes to consider the phylogenetic relationships of 50 Ophiostoma species, representing all the major morphological groups in the genus. Our data showed three well-supported, monophyletic lineages in Ophiostoma. Species with Leptographium anamorphs grouped together and to accommodate these species the teleomorph-genus Grosmannia (type species G. penicillata), including 27 species and 24 new combinations, is re-instated. Another well-defined lineage includes species that are cycloheximide-sensitive with short perithecial necks, falcate ascospores and Hyalorhinocladiella anamorphs. For these species, the teleomorph-genus Ceratocystiopsis (type species O. minuta), including 11 species and three new combinations, is re-instated. - 
												
												Biodiversity Sector Plan for the Zululand District Municipality, Kwazulu-Natal
EZEMVELO KZN WILDLIFE Biodiversity Sector Plan for the Zululand District Municipality, KwaZulu-Natal Technical Report February 2010 The Project Team Thorn-Ex cc (Environmental Services) PO Box 800, Hilton, 3245 Pietermaritzbur South Africa Tel: (033) 3431814 Fax: (033) 3431819 Mobile: 084 5014665 [email protected] Marita Thornhill (Project Management & Coordination) AFZELIA Environmental Consultants cc KwaZulu-Natal Western Cape PO Box 95 PO Box 3397 Hilton 3245 Cape Town 8000 Tel: 033 3432931/32 Tel: 072 3900686 Fax: 033 3432033 or Fax: 086 5132112 086 5170900 Mobile: 084 6756052 [email protected] [email protected] Wolfgang Kanz (Biodiversity Specialist Coordinator) John Richardson (GIS) Monde Nembula (Social Facilitation) Tim O’Connor & Associates P.O.Box 379 Hilton 3245 South Africa Tel/ Fax: 27-(0)33-3433491 [email protected] Tim O’Connor (Biodiversity Expert Advice) Zululand Biodiversity Sector Plan (February 2010) 1 Executive Summary The Biodiversity Act introduced several legislated planning tools to assist with the management and conservation of South Africa’s biological diversity. These include the declaration of “Bioregions” and the publication of “Bioregional Plans”. Bioregional plans are usually an output of a systematic spatial conservation assessment of a region. They identify areas of conservation priority, and constraints and opportunities for implementation of the plan. The precursor to a Bioregional Plan is a Biodiversity Sector Plan (BSP), which is the official reference for biodiversity priorities to be taken into account in land-use planning and decision-making by all sectors within the District Municipality. The overall aim is to avoid the loss of natural habitat in Critical Biodiversity Areas (CBAs) and prevent the degradation of Ecological Support Areas (ESAs), while encouraging sustainable development in Other Natural Areas. - 
												
												Fungal Allergy and Pathogenicity 20130415 112934.Pdf
Fungal Allergy and Pathogenicity Chemical Immunology Vol. 81 Series Editors Luciano Adorini, Milan Ken-ichi Arai, Tokyo Claudia Berek, Berlin Anne-Marie Schmitt-Verhulst, Marseille Basel · Freiburg · Paris · London · New York · New Delhi · Bangkok · Singapore · Tokyo · Sydney Fungal Allergy and Pathogenicity Volume Editors Michael Breitenbach, Salzburg Reto Crameri, Davos Samuel B. Lehrer, New Orleans, La. 48 figures, 11 in color and 22 tables, 2002 Basel · Freiburg · Paris · London · New York · New Delhi · Bangkok · Singapore · Tokyo · Sydney Chemical Immunology Formerly published as ‘Progress in Allergy’ (Founded 1939) Edited by Paul Kallos 1939–1988, Byron H. Waksman 1962–2002 Michael Breitenbach Professor, Department of Genetics and General Biology, University of Salzburg, Salzburg Reto Crameri Professor, Swiss Institute of Allergy and Asthma Research (SIAF), Davos Samuel B. Lehrer Professor, Clinical Immunology and Allergy, Tulane University School of Medicine, New Orleans, LA Bibliographic Indices. This publication is listed in bibliographic services, including Current Contents® and Index Medicus. Drug Dosage. The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any change in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means electronic or mechanical, including photocopying, recording, microcopy- ing, or by any information storage and retrieval system, without permission in writing from the publisher. - 
												
												Sequencing Abstracts Msa Annual Meeting Berkeley, California 7-11 August 2016
M S A 2 0 1 6 SEQUENCING ABSTRACTS MSA ANNUAL MEETING BERKELEY, CALIFORNIA 7-11 AUGUST 2016 MSA Special Addresses Presidential Address Kerry O’Donnell MSA President 2015–2016 Who do you love? Karling Lecture Arturo Casadevall Johns Hopkins Bloomberg School of Public Health Thoughts on virulence, melanin and the rise of mammals Workshops Nomenclature UNITE Student Workshop on Professional Development Abstracts for Symposia, Contributed formats for downloading and using locally or in a Talks, and Poster Sessions arranged by range of applications (e.g. QIIME, Mothur, SCATA). 4. Analysis tools - UNITE provides variety of analysis last name of primary author. Presenting tools including, for example, massBLASTer for author in *bold. blasting hundreds of sequences in one batch, ITSx for detecting and extracting ITS1 and ITS2 regions of ITS 1. UNITE - Unified system for the DNA based sequences from environmental communities, or fungal species linked to the classification ATOSH for assigning your unknown sequences to *Abarenkov, Kessy (1), Kõljalg, Urmas (1,2), SHs. 5. Custom search functions and unique views to Nilsson, R. Henrik (3), Taylor, Andy F. S. (4), fungal barcode sequences - these include extended Larsson, Karl-Hnerik (5), UNITE Community (6) search filters (e.g. source, locality, habitat, traits) for 1.Natural History Museum, University of Tartu, sequences and SHs, interactive maps and graphs, and Vanemuise 46, Tartu 51014; 2.Institute of Ecology views to the largest unidentified sequence clusters and Earth Sciences, University of Tartu, Lai 40, Tartu formed by sequences from multiple independent 51005, Estonia; 3.Department of Biological and ecological studies, and for which no metadata Environmental Sciences, University of Gothenburg, currently exists. - 
												
												New Xerophilic Species of Penicillium from Soil
Journal of Fungi Article New Xerophilic Species of Penicillium from Soil Ernesto Rodríguez-Andrade, Alberto M. Stchigel * and José F. Cano-Lira Mycology Unit, Medical School and IISPV, Universitat Rovira i Virgili (URV), Sant Llorenç 21, Reus, 43201 Tarragona, Spain; [email protected] (E.R.-A.); [email protected] (J.F.C.-L.) * Correspondence: [email protected]; Tel.: +34-977-75-9341 Abstract: Soil is one of the main reservoirs of fungi. The aim of this study was to study the richness of ascomycetes in a set of soil samples from Mexico and Spain. Fungi were isolated after 2% w/v phenol treatment of samples. In that way, several strains of the genus Penicillium were recovered. A phylogenetic analysis based on internal transcribed spacer (ITS), beta-tubulin (BenA), calmodulin (CaM), and RNA polymerase II subunit 2 gene (rpb2) sequences showed that four of these strains had not been described before. Penicillium melanosporum produces monoverticillate conidiophores and brownish conidia covered by an ornate brown sheath. Penicillium michoacanense and Penicillium siccitolerans produce sclerotia, and their asexual morph is similar to species in the section Aspergilloides (despite all of them pertaining to section Lanata-Divaricata). P. michoacanense differs from P. siccitol- erans in having thick-walled peridial cells (thin-walled in P. siccitolerans). Penicillium sexuale differs from Penicillium cryptum in the section Crypta because it does not produce an asexual morph. Its ascostromata have a peridium composed of thick-walled polygonal cells, and its ascospores are broadly lenticular with two equatorial ridges widely separated by a furrow. All four new species are xerophilic. - 
												
												NUMBERED TREE SPECIES LIST in SOUTH AFRICA CYATHEACEAE 1 Cyathea Dregei 2 Cyathea Capensis Var. Capensis ZAMIACEAE 3 Encephalart
NUMBERED TREE SPECIES LIST IN SOUTH AFRICA 23 Hyphaene coriacea CYATHEACEAE 24 Hyphaene petersiana 1 Cyathea dregei 25 Borassus aethiopum 2 Cyathea capensis var. capensis 26 Raphia australis 27 Jubaeopsis caffra ZAMIACEAE 3 Encephalartos altensteinii ASPHODELACEAE 3.1 Encephalartos eugene-maraisii 28 Aloe barberae 3.2 Encephalartos arenarius 28.1 Aloe arborescens 3.3 Encephalartos brevifoliolatus 28.2 Aloe africana 3.4 Encephalartos ferox 28.3 Aloe alooides 4 Encephalartos friderici-guilielmi 28.4 Aloe angelica 5 Encephalartos ghellinckii 28.5 Aloe candelabrum 5.1 Encephalartos inopinus 28.6 Aloe castanea 5.2 Encephalartos lanatus 28.7 Aloe comosa 6 Encephalartos laevifolius 28.8 Aloe excelsa var. excelsa 7 Encephalartos latifrons 29 Aloe dichotoma 8 Encephalartos senticosus 29.1 Aloe dolomitica 8.1 Encephalartos lehmannii 29.2 Aloe ferox 9 Encephalartos longifolius 29.3 Aloe khamiesensis 10 Encephalartos natalensis 29.4 Aloe littoralis 11 Encephalartos paucidentatus 29.5 Aloe marlothii subsp. marlothii 12 Encephalartos princeps 29.6 Aloe plicatilis 12.5 Encephalartos relictus 29.7 Aloe marlothii subsp. orientalis 13 Encephalartos transvenosus 30 Aloe pillansii 14 Encephalartos woodii 30.1 Aloe pluridens 14.1 Encephalartos heenanii 30.2 Aloe ramosissima 14.2 Encephalartos dyerianus 30.3 Aloe rupestris 14.3 Encephalartos middelburgensis 30.4 Aloe spicata 14.4 Encephalartos dolomiticus 30.5 Aloe speciosa 14.5 Encephalartos aemulans 30.6 Aloe spectabilis 14.6 Encephalartos hirsutus 30.7 Aloe thraskii 14.7 Encephalartos msinganus 14.8 Encephalartos - 
												
												Sporotrichosis
8/6/2011 Sporotrichosis • Alternative name –Rose Handler’s Disease Named due to fungal infection resulting from thorn pricks or barbs, Sporotrichosis handling of sphagnum moss or by slivers from Pam Galioto, Megan Lileas, Tom wood or lumber Mariani, and Katie Olenick – Kingdom: Fungi • Only one active species – Phylum: Ascomycota –Sporothrix schenckii • Thermally dimorphic – Class: Euascomycetes fungus which is distributed worldwide – Order: Ophiostomatales • Isolated from soil, living and decomposing plants, woods, and peat moss – Family: Ophiostomataceae – Genus: Sporothrix Geographical Distribution Life Cycle Phase 1 – Hyphal Phase • Exists worldwide, but uncommon in •25°C, grows slowly United States •Conidospores • Peru has hyperendemicity for infection •Pigmented white, cream, or black • More common in temperate or tropical •Flower formation zones Phase 2 – Yeast Phase •37°C •Pigmented white or greyish-yellow •Spherical/budding yeast colonies 1 8/6/2011 Epidemiology Pathogenesis At risk - Prevention – •Generally enters body through skin •Handling thorny plants, baled •Wear gloves when handling prick, cuts, or small punctures hay, moss wires, bushes, etc. •Can be inhaled •Nursery workers •Avoid contact with •Cutaneous, pulmonary, or •Children playing on baled hay sphagnum moss disseminated infection •Rose gardeners •Proper handling of •Joints, lungs, and central nervous •Greenhouse workers laboratory equipment system have occurred •First nodule in 1 to 12 weeks •Can infect animals •Can cause arthritis, meningitis, pneumonitis, or