Macrofungal Diversity Associated with the Scale-Leaf Juniper Trees, Juniperus Excelsa and J
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Annotated Check List and Host Index Arizona Wood
Annotated Check List and Host Index for Arizona Wood-Rotting Fungi Item Type text; Book Authors Gilbertson, R. L.; Martin, K. J.; Lindsey, J. P. Publisher College of Agriculture, University of Arizona (Tucson, AZ) Rights Copyright © Arizona Board of Regents. The University of Arizona. Download date 28/09/2021 02:18:59 Link to Item http://hdl.handle.net/10150/602154 Annotated Check List and Host Index for Arizona Wood - Rotting Fungi Technical Bulletin 209 Agricultural Experiment Station The University of Arizona Tucson AÏfJ\fOTA TED CHECK LI5T aid HOST INDEX ford ARIZONA WOOD- ROTTlNg FUNGI /. L. GILßERTSON K.T IyIARTiN Z J. P, LINDSEY3 PRDFE550I of PLANT PATHOLOgY 2GRADUATE ASSISTANT in I?ESEARCI-4 36FZADAATE A5 S /STANT'" TEACHING Z z l'9 FR5 1974- INTRODUCTION flora similar to that of the Gulf Coast and the southeastern United States is found. Here the major tree species include hardwoods such as Arizona is characterized by a wide variety of Arizona sycamore, Arizona black walnut, oaks, ecological zones from Sonoran Desert to alpine velvet ash, Fremont cottonwood, willows, and tundra. This environmental diversity has resulted mesquite. Some conifers, including Chihuahua pine, in a rich flora of woody plants in the state. De- Apache pine, pinyons, junipers, and Arizona cypress tailed accounts of the vegetation of Arizona have also occur in association with these hardwoods. appeared in a number of publications, including Arizona fungi typical of the southeastern flora those of Benson and Darrow (1954), Nichol (1952), include Fomitopsis ulmaria, Donkia pulcherrima, Kearney and Peebles (1969), Shreve and Wiggins Tyromyces palustris, Lopharia crassa, Inonotus (1964), Lowe (1972), and Hastings et al. -
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. -
A Preliminary Checklist of Arizona Macrofungi
A PRELIMINARY CHECKLIST OF ARIZONA MACROFUNGI Scott T. Bates School of Life Sciences Arizona State University PO Box 874601 Tempe, AZ 85287-4601 ABSTRACT A checklist of 1290 species of nonlichenized ascomycetaceous, basidiomycetaceous, and zygomycetaceous macrofungi is presented for the state of Arizona. The checklist was compiled from records of Arizona fungi in scientific publications or herbarium databases. Additional records were obtained from a physical search of herbarium specimens in the University of Arizona’s Robert L. Gilbertson Mycological Herbarium and of the author’s personal herbarium. This publication represents the first comprehensive checklist of macrofungi for Arizona. In all probability, the checklist is far from complete as new species await discovery and some of the species listed are in need of taxonomic revision. The data presented here serve as a baseline for future studies related to fungal biodiversity in Arizona and can contribute to state or national inventories of biota. INTRODUCTION Arizona is a state noted for the diversity of its biotic communities (Brown 1994). Boreal forests found at high altitudes, the ‘Sky Islands’ prevalent in the southern parts of the state, and ponderosa pine (Pinus ponderosa P.& C. Lawson) forests that are widespread in Arizona, all provide rich habitats that sustain numerous species of macrofungi. Even xeric biomes, such as desertscrub and semidesert- grasslands, support a unique mycota, which include rare species such as Itajahya galericulata A. Møller (Long & Stouffer 1943b, Fig. 2c). Although checklists for some groups of fungi present in the state have been published previously (e.g., Gilbertson & Budington 1970, Gilbertson et al. 1974, Gilbertson & Bigelow 1998, Fogel & States 2002), this checklist represents the first comprehensive listing of all macrofungi in the kingdom Eumycota (Fungi) that are known from Arizona. -
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Hilton et al. Microbiome (2021) 9:19 https://doi.org/10.1186/s40168-020-00972-0 RESEARCH Open Access Identification of microbial signatures linked to oilseed rape yield decline at the landscape scale Sally Hilton1* , Emma Picot1, Susanne Schreiter2, David Bass3,4, Keith Norman5, Anna E. Oliver6, Jonathan D. Moore7, Tim H. Mauchline2, Peter R. Mills8, Graham R. Teakle1, Ian M. Clark2, Penny R. Hirsch2, Christopher J. van der Gast9 and Gary D. Bending1* Abstract Background: The plant microbiome plays a vital role in determining host health and productivity. However, we lack real-world comparative understanding of the factors which shape assembly of its diverse biota, and crucially relationships between microbiota composition and plant health. Here we investigated landscape scale rhizosphere microbial assembly processes in oilseed rape (OSR), the UK’s third most cultivated crop by area and the world's third largest source of vegetable oil, which suffers from yield decline associated with the frequency it is grown in rotations. By including 37 conventional farmers’ fields with varying OSR rotation frequencies, we present an innovative approach to identify microbial signatures characteristic of microbiomes which are beneficial and harmful to the host. Results: We show that OSR yield decline is linked to rotation frequency in real-world agricultural systems. We demonstrate fundamental differences in the environmental and agronomic drivers of protist, bacterial and fungal communities between root, rhizosphere soil and bulk soil compartments. We further discovered that the assembly of fungi, but neither bacteria nor protists, was influenced by OSR rotation frequency. However, there were individual abundant bacterial OTUs that correlated with either yield or rotation frequency. -
Re-Thinking the Classification of Corticioid Fungi
mycological research 111 (2007) 1040–1063 journal homepage: www.elsevier.com/locate/mycres Re-thinking the classification of corticioid fungi Karl-Henrik LARSSON Go¨teborg University, Department of Plant and Environmental Sciences, Box 461, SE 405 30 Go¨teborg, Sweden article info abstract Article history: Corticioid fungi are basidiomycetes with effused basidiomata, a smooth, merulioid or Received 30 November 2005 hydnoid hymenophore, and holobasidia. These fungi used to be classified as a single Received in revised form family, Corticiaceae, but molecular phylogenetic analyses have shown that corticioid fungi 29 June 2007 are distributed among all major clades within Agaricomycetes. There is a relative consensus Accepted 7 August 2007 concerning the higher order classification of basidiomycetes down to order. This paper Published online 16 August 2007 presents a phylogenetic classification for corticioid fungi at the family level. Fifty putative Corresponding Editor: families were identified from published phylogenies and preliminary analyses of unpub- Scott LaGreca lished sequence data. A dataset with 178 terminal taxa was compiled and subjected to phy- logenetic analyses using MP and Bayesian inference. From the analyses, 41 strongly Keywords: supported and three unsupported clades were identified. These clades are treated as fam- Agaricomycetes ilies in a Linnean hierarchical classification and each family is briefly described. Three ad- Basidiomycota ditional families not covered by the phylogenetic analyses are also included in the Molecular systematics classification. All accepted corticioid genera are either referred to one of the families or Phylogeny listed as incertae sedis. Taxonomy ª 2007 The British Mycological Society. Published by Elsevier Ltd. All rights reserved. Introduction develop a downward-facing basidioma. -
Host„&Ndash;„Pathogen Interactions in Relation To
CSIRO PUBLISHING Crop & Pasture Science, 2018, 69,9–19 http://dx.doi.org/10.1071/CP16445 Host–pathogen interactions in relation to management of light leaf spot disease (caused by Pyrenopeziza brassicae) on Brassica species Chinthani S. Karandeni Dewage A,B, Coretta A. Klöppel A, Henrik U. Stotz A, and Bruce D. L. Fitt A ASchool of Life and Medical Sciences, University of Hertfordshire, Hatfield, Hertfordshire, AL10 9AB, UK. BCorresponding author. Email: [email protected] Abstract. Light leaf spot, caused by Pyrenopeziza brassicae, is the most damaging disease problem in oilseed rape (Brassica napus) in the United Kingdom. According to recent survey data, the severity of epidemics has increased progressively across the UK, with yield losses of up to £160M per annum in England and more severe epidemics in Scotland. Light leaf spot is a polycyclic disease, with primary inoculum consisting of airborne ascospores produced on diseased debris from the previous cropping season. Splash-dispersed conidia produced on diseased leaves are the main component of the secondary inoculum. Pyrenopeziza brassicae is also able to infect and cause considerable yield losses on vegetable brassicas, especially Brussels sprouts. There may be spread of light leaf spot among different Brassica species. Since they have a wide host range and frequent occurrence of sexual reproduction, P. brassicae populations are likely to have considerable genetic diversity, and evidence suggests population variations between different geographic regions, which need further study. Available disease-management tools are not sufficient to provide adequate control of the disease. There is a need to identify new sources of resistance, which can be integrated with fungicide applications to achieve sustainable management of light leaf spot. -
Biodiversity and Coarse Woody Debris in Southern Forests Proceedings of the Workshop on Coarse Woody Debris in Southern Forests: Effects on Biodiversity
Biodiversity and Coarse woody Debris in Southern Forests Proceedings of the Workshop on Coarse Woody Debris in Southern Forests: Effects on Biodiversity Athens, GA - October 18-20,1993 Biodiversity and Coarse Woody Debris in Southern Forests Proceedings of the Workhop on Coarse Woody Debris in Southern Forests: Effects on Biodiversity Athens, GA October 18-20,1993 Editors: James W. McMinn, USDA Forest Service, Southern Research Station, Forestry Sciences Laboratory, Athens, GA, and D.A. Crossley, Jr., University of Georgia, Athens, GA Sponsored by: U.S. Department of Energy, Savannah River Site, and the USDA Forest Service, Savannah River Forest Station, Biodiversity Program, Aiken, SC Conducted by: USDA Forest Service, Southem Research Station, Asheville, NC, and University of Georgia, Institute of Ecology, Athens, GA Preface James W. McMinn and D. A. Crossley, Jr. Conservation of biodiversity is emerging as a major goal in The effects of CWD on biodiversity depend upon the management of forest ecosystems. The implied harvesting variables, distribution, and dynamics. This objective is the conservation of a full complement of native proceedings addresses the current state of knowledge about species and communities within the forest ecosystem. the influences of CWD on the biodiversity of various Effective implementation of conservation measures will groups of biota. Research priorities are identified for future require a broader knowledge of the dimensions of studies that should provide a basis for the conservation of biodiversity, the contributions of various ecosystem biodiversity when interacting with appropriate management components to those dimensions, and the impact of techniques. management practices. We thank John Blake, USDA Forest Service, Savannah In a workshop held in Athens, GA, October 18-20, 1993, River Forest Station, for encouragement and support we focused on an ecosystem component, coarse woody throughout the workshop process. -
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 Checklist of the Aphyllophoroid Fungi (Basidiomycota) Recorded from the Brazilian Atlantic Forest
Posted date: September 2009 Summary published in MYCOTAXON 109: 439–442 A checklist of the aphyllophoroid fungi (Basidiomycota) recorded from the Brazilian Atlantic Forest JULIANO MARCON BALTAZAR & TATIANA BAPTISTA GIBERTONI [email protected], [email protected] Universidade Federal de Pernambuco, Departamento de Micologia Av. Nelson Chaves s/n, CEP 50670-420, Recife, Pernambuco, Brazil Abstract — The Atlantic Forest is one of the most diverse and threatened biomes of the world. A list with 733 species of aphyllophoroid fungi reported from the Brazilian Altantic Forest is presented based on an intensive search of literature records. These species are distributed in 219 genera and 47 families. Polyporaceae is the most highly represented family with 153 species; Phellinus is the genus with the highest number of species (42). Key words — Aphyllophorales, macrofungi, neotropics Introduction The Atlantic Forest is a unique series of South American rainforest ecosystems, which also includes other distinct vegetation types, such as mangroves and ‘restinga’ (Mittermeier et al. 2005). This biome is located along the Atlantic coast of Brazil and inland into parts of Argentine and Paraguay. It once covered an area of approximately 1,300,000 km2 (Pôrto et al. 2006), and it was present in 17 of the 27 states of Brazil. This rainforest is one of the most diverse regions and one of the most threatened environments of the world, since its area is now home to 67% of the Brazilian population and it is currently reduced to 7.26% of its original size, placing it among the five most important hotspots (Mittermeier 2005, SOS Mata Atlântica/INPE 2008). -
Genera of Corticioid Fungi: Keys, Nomenclature and Taxonomy Article
Studies in Fungi 5(1): 125–309 (2020) www.studiesinfungi.org ISSN 2465-4973 Article Doi 10.5943/sif/5/1/12 Genera of corticioid fungi: keys, nomenclature and taxonomy Gorjón SP BIOCONS – Department of Botany and Plant Physiology, University of Salamanca, 37007 Salamanca, Spain Gorjón SP 2020 – Genera of corticioid fungi: keys, nomenclature, and taxonomy. Studies in Fungi 5(1), 125–309, Doi 10.5943/sif/5/1/12 Abstract A review of the worldwide corticioid homobasidiomycetes genera is presented. A total of 620 genera are considered with comments on their taxonomy and nomenclature. Of them, about 420 are accepted and keyed out, described in detail with remarks on their taxonomy and systematics. Key words – Corticiaceae – Crust fungi – Diversity – Homobasidiomycetes Introduction Corticioid fungi are a diverse and heterogeneous group of fungi mainly referred to basidiomycete fungi in which basidiomes are generally resupinate. Basidiome construction is often simple, and in most cases, only generative hyphae are found. In more structured basidiomes, those with a reflexed margin or with a pileate surface, more or less sclerified hyphae are usually found. Even the basidiome structure is apparently not very complex, hymenophore configuration should be highly variable finding smooth surfaces or different variations to increase the spore production area such as rugose, tuberculate, aculeate, merulioid, folded, or poroid hymenial surfaces. It is often thought that corticioid fungi produce unattractive and little variable forms and, in most cases, they go unnoticed by most mycologists as ungraceful forms that ‘cover sticks and look like a paint stain’. Although the macroscopic variability compared to other fungi is, but not always, usually limited, under the microscope they surprise with a great diversity of forms of basidia, cystidia, spores and other microscopic elements (Hjortstam et al. -
Light Leaf Spot and White Leaf Spot of Brassicaceae in Washington State
LIGHT LEAF SPOT AND WHITE LEAF SPOT OF BRASSICACEAE IN WASHINGTON STATE By SHANNON MARIE CARMODY A thesis submitted in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE IN PLANT PATHOLOGY WASHINGTON STATE UNIVERSITY Department of Plant Pathology JULY 2017 © Copyright by SHANNON MARIE CARMODY, 2017 All Rights Reserved To the Faculty of Washington State University: The members of the Committee appointed to examine the thesis of SHANNON MARIE CARMODY find it satisfactory and recommend that it be accepted. Lindsey J. du Toit, Ph.D., Chair Lori M. Carris, Ph.D. Timothy C. Paulitz, Ph.D. Cynthia M. Ocamb, Ph.D. ii ACKNOWLEDGMENT I would like to thank my major advisor Dr. Lindsey du Toit for her tireless mentorship, passion, and enthusiasm. I wish to thanks my committee members Dr. Lori Carris, Dr. Cynthia Ocamb, and Dr. Timothy Paulitz who welcomed me into their labs in Pullman, WA and when visiting in Corvallis, OR. This work would not have been possible without the financial support of the Clif Bar Family Foundation Seed Matters Initiative and the Western Sustainable Agriculture Research and Education Fellowship. Thank you to all of the faculty, students, and staff of WSU Mount Vernon and WSU Pullman who have generously shared time, support, knowledge, tulips, equipment, and humor. As was noted in my hospital chart, you all made sure I was “emotionally, financially, and botanically supported” which is more than I could have ever asked for. None of my research would have been possible without the members of the Vegetable Seed Pathology Lab. -
Mollisia Friday, 22 March 2019 9:46 PM
Mollisia Friday, 22 March 2019 9:46 PM These notes were Initially prepared in late 2017, additional species have subsequently been collected in NZ, but this summary gives an idea of the diversity present in NZs native forests, and its relationship to that found in the rest of the world. Data is presented as an ITS gene tree, comparing the 50 or so New Zealand Mollisia and Mollisia-like species for which there are cultures, to specimens treated by Joey Tanney (2016; Phialocephala) , Brian Douglas (2013, PhD thesis), and Genbank BLAST matches to accessions from type specimens (Ascocoryne, Helicodendron and Dimorphospora (Gelatinodiscaceae) as outgroups). UNITE Species Hypothesis matches are noted. Morphology has barely been compared, but in the case of NZ Species 31 morphology does not support the ITS-based genetic match. Any matches need confirming with a more discriminatory gene; RPB1 has been used by Tanney and others. Generic limits remain poorly resolved. Data in Geneious Dan Discos\28 Sept 2017\Mollisia 'Mollisia' in the sense discussed here includes most of the New Zealand specimens having a sexual fruiting body with a Dermateaceae morphology in the sense of Korf (non-gelatinous excipulum of more or less globose cells, usually with dark walls) that have an ITS sequence available, in morphologically defined genera such as Mollisia, Pyrenopeziza, Niptera, and Tapesia. Also included are the (as yet unpublished) sequences from the Mollisia PhD thesis of Brian Douglas, the Phialocephala sequences from Joey Tanney (2016), and sequences that represent type specimens from Genbank BLAST search results based on the New Zealand sequences.