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Mating-Type Locus Organization and Mating-Type Chromosome Differentiation in the Bipolar Edible Button Mushroom Agaricus Bisporus
G C A T T A C G G C A T genes Article Mating-Type Locus Organization and Mating-Type Chromosome Differentiation in the Bipolar Edible Button Mushroom Agaricus bisporus Marie Foulongne-Oriol 1 , Ozgur Taskent 2, Ursula Kües 3, Anton S. M. Sonnenberg 4, Arend F. van Peer 4 and Tatiana Giraud 2,* 1 INRAE, MycSA, Mycologie et Sécurité des Aliments, 33882 Villenave d’Ornon, France; [email protected] 2 Ecologie Systématique Evolution, Bâtiment 360, CNRS, AgroParisTech, Université Paris-Saclay, 91400 Orsay, France; [email protected] 3 Molecular Wood Biotechnology and Technical Mycology, Goettingen Center for Molecular Biosciences (GZMB), Büsgen-Institute, University of Goettingen, Büsgenweg 2, 37077 Goettingen, Germany; [email protected] 4 Plant Breeding, Wageningen University and Research, Droevendaalsesteeg 1, 6708 PB Wageningen, The Netherlands; [email protected] (A.S.M.S.); [email protected] (A.F.v.P.) * Correspondence: [email protected] Abstract: In heterothallic basidiomycete fungi, sexual compatibility is restricted by mating types, typically controlled by two loci: PR, encoding pheromone precursors and pheromone receptors, and HD, encoding two types of homeodomain transcription factors. We analysed the single mating-type locus of the commercial button mushroom variety, Agaricus bisporus var. bisporus, and of the related Citation: Foulongne-Oriol, M.; variety burnettii. We identified the location of the mating-type locus using genetic map and genome Taskent, O.; Kües, U.; Sonnenberg, information, corresponding to the HD locus, the PR locus having lost its mating-type role. We A.S.M.; van Peer, A.F.; Giraud, T. -
Fungal Diversity in the Mediterranean Area
Fungal Diversity in the Mediterranean Area • Giuseppe Venturella Fungal Diversity in the Mediterranean Area Edited by Giuseppe Venturella Printed Edition of the Special Issue Published in Diversity www.mdpi.com/journal/diversity Fungal Diversity in the Mediterranean Area Fungal Diversity in the Mediterranean Area Editor Giuseppe Venturella MDPI • Basel • Beijing • Wuhan • Barcelona • Belgrade • Manchester • Tokyo • Cluj • Tianjin Editor Giuseppe Venturella University of Palermo Italy Editorial Office MDPI St. Alban-Anlage 66 4052 Basel, Switzerland This is a reprint of articles from the Special Issue published online in the open access journal Diversity (ISSN 1424-2818) (available at: https://www.mdpi.com/journal/diversity/special issues/ fungal diversity). For citation purposes, cite each article independently as indicated on the article page online and as indicated below: LastName, A.A.; LastName, B.B.; LastName, C.C. Article Title. Journal Name Year, Article Number, Page Range. ISBN 978-3-03936-978-2 (Hbk) ISBN 978-3-03936-979-9 (PDF) c 2020 by the authors. Articles in this book are Open Access and distributed under the Creative Commons Attribution (CC BY) license, which allows users to download, copy and build upon published articles, as long as the author and publisher are properly credited, which ensures maximum dissemination and a wider impact of our publications. The book as a whole is distributed by MDPI under the terms and conditions of the Creative Commons license CC BY-NC-ND. Contents About the Editor .............................................. vii Giuseppe Venturella Fungal Diversity in the Mediterranean Area Reprinted from: Diversity 2020, 12, 253, doi:10.3390/d12060253 .................... 1 Elias Polemis, Vassiliki Fryssouli, Vassileios Daskalopoulos and Georgios I. -
Part 2 – Fruticose Species
Appendix 5.2-1 Vegetation Technical Appendix APPENDIX 5.2‐1 Vegetation Technical Appendix Contents Section Page Ecological Land Classification ............................................................................................................ A5.2‐1‐1 Geodatabase Development .............................................................................................. A5.2‐1‐1 Vegetation Community Mapping ..................................................................................... A5.2‐1‐1 Quality Assurance and Quality Control ............................................................................ A5.2‐1‐3 Limitations of Ecological Land Classification .................................................................... A5.2‐1‐3 Field Data Collection ......................................................................................................... A5.2‐1‐3 Supplementary Results ..................................................................................................... A5.2‐1‐4 Rare Vegetation Species and Rare Ecological Communities ........................................................... A5.2‐1‐10 Supplementary Desktop Results ..................................................................................... A5.2‐1‐10 Field Methods ................................................................................................................. A5.2‐1‐16 Supplementary Results ................................................................................................... A5.2‐1‐17 Weed Species -
Draft Genome Sequence of a Monokaryotic
Draft genome sequence of a monokaryotic model brown-rot fungus Postia (Rhodonia) placenta SB12 Jill Gaskell, Phil Kersten, Luis Larrondo, Paulo Canessa, Diego Martínez, David Hibbett, Monika Schmoll, Christian Kubicek, Angel Martinez, Jagjit Yadav, et al. To cite this version: Jill Gaskell, Phil Kersten, Luis Larrondo, Paulo Canessa, Diego Martínez, et al.. Draft genome sequence of a monokaryotic model brown-rot fungus Postia (Rhodonia) placenta SB12. Genomics Data, Elsevier, 2017, 14, pp.21-23. 10.1016/j.gdata.2017.08.003. hal-01802856 HAL Id: hal-01802856 https://hal.archives-ouvertes.fr/hal-01802856 Submitted on 8 Jun 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution| 4.0 International License Genomics Data 14 (2017) 21–23 Contents lists available at ScienceDirect Genomics Data journal homepage: www.elsevier.com/locate/gdata Data in Brief Draft genome sequence of a monokaryotic model brown-rot fungus Postia MARK (Rhodonia) placenta SB12 Jill Gaskella, Phil Kerstena, Luis F. Larrondob, Paulo Canessab,c, Diego Martinezd,1, David Hibbette, Monika Schmollf, Christian P. Kubicekg, Angel T. Martinezh, Jagjit Yadavi, Emma Masterj, Jon Karl Magnusonk, Debbie Yaverl, Randy Berkal, Kathleen Lailm, Cindy Chenm, Kurt LaButtim, Matt Nolanm, Anna Lipzenm, Andrea Aertsm, Robert Rileym, Kerrie Barrym, ⁎ Bernard Henrissatn,o,p,q, Robert Blanchetter, Igor V. -
Universidade Federal De Santa Catarina Para a Obtenção Do Grau De Mestre Em Biologia De Fungos, Algas E Plantas
0 Gesieli Kaipper Figueiró ASPECTOS TAXONÔMICOS E FILOGENÉTICOS DE Antrodia s.l. COM A INCLUSÃO DE ESPÉCIMES DA REGIÃO NEOTROPICAL Dissertação submetida ao Programa de Pós Graduação em Biologia de Fungos, Algas e Plantas da Universidade Federal de Santa Catarina para a obtenção do Grau de mestre em Biologia de Fungos, Algas e Plantas. Orientador: Prof. Dr. Elisandro Ricardo Drechsler dos Santos. Coorientador: Dr. Gerardo Lucio Robledo. Florianópolis 2015 1 2 3 AGRADECIMENTOS Aos meus orientadores Ricardo e Gerardo, pelo aprendizado, confiança e disponibilidade durante esses dois anos, não tenho palavras para agradecê-los; Aos professores do programa de Pós-Graduação em Biologia de Fungos, Algas e Plantas pelo conhecimento transmitido durante a realização das disciplinas; Agradeço aos curadores dos Herbários CORD, FLOR, IBOT e URM, pelos empréstimos de materiais; Agradeço à Prof.ª Maria Alice pelo conhecimento transmitido e por todas as conversas e experiências no micolab; Ao Mateus Arduvino Reck pela amizade, aprendizado e disponibilidade para me ajudar sempre; Ao Dr. Aristóteles Góes Neto, que por meio do projeto “FungiBrBol” forneceu subsídios indispensáveis para a execução das análises moleculares deste trabalho; Agradeço imensamente a Val, Diogo e Carlos que tiveram toda a paciência do mundo me ensinando as coisas mais básicas e lindas sobre o mundo dos Fungos; Também sou grata aos colegas do Micolab pela amizade e carinho de sempre, compartilhando momentos de alegrias e tristezas, almoços de domingos e todas as datas comemorativas -
Washington Flora Checklist a Checklist of the Vascular Plants of Washington State Hosted by the University of Washington Herbarium
Washington Flora Checklist A checklist of the Vascular Plants of Washington State Hosted by the University of Washington Herbarium The Washington Flora Checklist aims to be a complete list of the native and naturalized vascular plants of Washington State, with current classifications, nomenclature and synonymy. The checklist currently contains 3,929 terminal taxa (species, subspecies, and varieties). Taxa included in the checklist: * Native taxa whether extant, extirpated, or extinct. * Exotic taxa that are naturalized, escaped from cultivation, or persisting wild. * Waifs (e.g., ballast plants, escaped crop plants) and other scarcely collected exotics. * Interspecific hybrids that are frequent or self-maintaining. * Some unnamed taxa in the process of being described. Family classifications follow APG IV for angiosperms, PPG I (J. Syst. Evol. 54:563?603. 2016.) for pteridophytes, and Christenhusz et al. (Phytotaxa 19:55?70. 2011.) for gymnosperms, with a few exceptions. Nomenclature and synonymy at the rank of genus and below follows the 2nd Edition of the Flora of the Pacific Northwest except where superceded by new information. Accepted names are indicated with blue font; synonyms with black font. Native species and infraspecies are marked with boldface font. Please note: This is a working checklist, continuously updated. Use it at your discretion. Created from the Washington Flora Checklist Database on September 17th, 2018 at 9:47pm PST. Available online at http://biology.burke.washington.edu/waflora/checklist.php Comments and questions should be addressed to the checklist administrators: David Giblin ([email protected]) Peter Zika ([email protected]) Suggested citation: Weinmann, F., P.F. Zika, D.E. Giblin, B. -
(Largeflower Triteleia): a Technical Conservation Assessment
Triteleia grandiflora Lindley (largeflower triteleia): A Technical Conservation Assessment © 2003 Ben Legler Prepared for the USDA Forest Service, Rocky Mountain Region, Species Conservation Project January 29, 2007 Juanita A. R. Ladyman, Ph.D. JnJ Associates LLC 6760 S. Kit Carson Cir E. Centennial, CO 80122 Peer Review Administered by Society for Conservation Biology Ladyman, J.A.R. (2007, January 29). Triteleia grandiflora Lindley (largeflower triteleia): a technical conservation assessment. [Online]. USDA Forest Service, Rocky Mountain Region. Available: http://www.fs.fed.us/r2/ projects/scp/assessments/triteleiagrandiflora.pdf [date of access]. ACKNOWLEDGMENTS The time spent and the help given by all the people and institutions mentioned in the References section are gratefully acknowledged. I would also like to thank the Colorado Natural Heritage Program for their generosity in making their files and records available. I also appreciate access to the files and assistance given to me by Andrew Kratz, USDA Forest Service Region 2. The data provided by the Wyoming Natural Diversity Database and by James Cosgrove and Lesley Kennes with the Natural History Collections Section, Royal BC Museum were invaluable in the preparation of the assessment. Documents and information provided by Michael Piep with the Intermountain Herbarium, Leslie Stewart and Cara Gildar of the San Juan National Forest, Jim Ozenberger of the Bridger-Teton National Forest and Peggy Lyon with the Colorado Natural Heritage Program are also gratefully acknowledged. The information provided by Dr. Ronald Hartman and B. Ernie Nelson with the Rocky Mountain Herbarium, Teresa Prendusi with the Region 4 USDA Forest Service, Klara Varga with the Grand Teton National Park, Jennifer Whipple with Yellowstone National Park, Dave Dyer with the University of Montana Herbarium, Caleb Morse of the R.L. -
A Revised Family-Level Classification of the Polyporales (Basidiomycota)
fungal biology 121 (2017) 798e824 journal homepage: www.elsevier.com/locate/funbio A revised family-level classification of the Polyporales (Basidiomycota) Alfredo JUSTOa,*, Otto MIETTINENb, Dimitrios FLOUDASc, € Beatriz ORTIZ-SANTANAd, Elisabet SJOKVISTe, Daniel LINDNERd, d €b f Karen NAKASONE , Tuomo NIEMELA , Karl-Henrik LARSSON , Leif RYVARDENg, David S. HIBBETTa aDepartment of Biology, Clark University, 950 Main St, Worcester, 01610, MA, USA bBotanical Museum, University of Helsinki, PO Box 7, 00014, Helsinki, Finland cDepartment of Biology, Microbial Ecology Group, Lund University, Ecology Building, SE-223 62, Lund, Sweden dCenter for Forest Mycology Research, US Forest Service, Northern Research Station, One Gifford Pinchot Drive, Madison, 53726, WI, USA eScotland’s Rural College, Edinburgh Campus, King’s Buildings, West Mains Road, Edinburgh, EH9 3JG, UK fNatural History Museum, University of Oslo, PO Box 1172, Blindern, NO 0318, Oslo, Norway gInstitute of Biological Sciences, University of Oslo, PO Box 1066, Blindern, N-0316, Oslo, Norway article info abstract Article history: Polyporales is strongly supported as a clade of Agaricomycetes, but the lack of a consensus Received 21 April 2017 higher-level classification within the group is a barrier to further taxonomic revision. We Accepted 30 May 2017 amplified nrLSU, nrITS, and rpb1 genes across the Polyporales, with a special focus on the Available online 16 June 2017 latter. We combined the new sequences with molecular data generated during the Poly- Corresponding Editor: PEET project and performed Maximum Likelihood and Bayesian phylogenetic analyses. Ursula Peintner Analyses of our final 3-gene dataset (292 Polyporales taxa) provide a phylogenetic overview of the order that we translate here into a formal family-level classification. -
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. -
Plants of Hot Springs Valley and Grover Hot Springs State Park Alpine County, California
Plants of Hot Springs Valley and Grover Hot Springs State Park Alpine County, California Compiled by Tim Messick and Ellen Dean This is a checklist of vascular plants that occur in Hot Springs Valley, including most of Grover Hot Springs State Park, in Alpine County, California. Approximately 310 taxa (distinct species, subspecies, and varieties) have been found in this area. How to Use this List Plants are listed alphabetically, by family, within major groups, according to their scientific names. This is standard practice for plant lists, but isn’t the most user-friendly for people who haven’t made a study of plant taxonomy. Identifying species in some of the larger families (e.g. the Sunflowers, Grasses, and Sedges) can become very technical, requiring examination of many plant characteristics under high magnification. But not to despair—many genera and even species of plants in this list become easy to recognize in the field with only a modest level of study or help from knowledgeable friends. Persistence will be rewarded with wonder at the diversity of plant life around us. Those wishing to pursue plant identification a bit further are encouraged to explore books on plants of the Sierra Nevada, and visit CalPhotos (calphotos.berkeley.edu), the Jepson eFlora (ucjeps.berkeley.edu/eflora), and CalFlora (www.calflora.org). The California Native Plant Society (www.cnps.org) promotes conservation of plants and their habitats throughout California and is a great resource for learning and for connecting with other native plant enthusiasts. The Nevada Native Plant Society nvnps.org( ) provides a similar focus on native plants of Nevada. -
A Journey Across Genomes Uncovers the Origin of Ubiquinone in Cyanobacteria
GBE A Journey across Genomes Uncovers the Origin of Ubiquinone in Cyanobacteria Mauro Degli Esposti1,2,* 1Italian Institute of Technology, Genoa, Italy 2Center for Genomic Sciences, Universidad National Autonoma de Mexico Campus of Cuernavaca, Cuernavaca, Morelos, Mexico *Corresponding author: E-mail: [email protected]. Accepted: October 31, 2017 Abstract Ubiquinone (Q) is an isoprenoid quinone that functions as membrane electron carrier in mitochondria and bacterial organisms belonging to the alpha, beta, and gamma class of proteobacteria. The biosynthesis of Q follows various biochemical steps catalyzed by diverse proteins that are, in general, homologous in mitochondria and bacteria. Nonorthologous proteins can also contribute to some biochemical steps as originally uncovered in Escherichia coli,which is the best studied organism for Q biosynthesis in prokaryotes. However, the origin of the biosynthetic pathway of Q has remained obscure. Here, I show by genome analysis that Q biosynthesis originated in cyanobacteria and then diversified in anaerobic alpha proteobacteria which have extant relatives in members of the Rhodospirillaceae family. Two distinct biochemical pathways diverged when ambient oxygen reached current levels on earth, one leading to the well-known series of Ubi genes found in E. coli, and the other containing CoQ proteins originally found in eukaryotes. Extant alpha proteobacteria show Q biosynthesis pathways that are more similar to that present in mitochondria than to that of E. coli. Hence, this work clarifies not only the origin but also the evolution of Q biosynthesis from bacteria to mitochondria. Key words: ubiquinone, menaquinone, plastoquinone, quinone biosynthesis, evolution of mitochondria. Introduction higher for Q; 2) the biosynthetic pathway of Q, which is pre- Ubiquinone (Q) is an isoprenoid substituted benzoquinone dominantly membrane-associated and requires oxygen in which shuttles electrons between membrane-bound respira- multiple steps. -
Avonlea Badlands Plant List
vonlea Badlands Plant List – 2019 Latin Name Common Name Achillea millefolium Common Yarrow Agoseris glauca False Dandelion Agropyron cristatum Crested Wheatgrass Allium textile Prairie Onion Amelanchier alnifolia Saskatoon Androsace septentrionalis Pygmyflower Anemone cylindrica Long-fruited Anemone Anemone patens Prairie Crocus Antennaria sp. Pussytoes Arabis pycnocarpa var. pycnocarpa Hairy Rockcress Arnica fulgens Shining-leaved Arnica Artemisia cana Sagebrush Artemisia frigida Pasture Sage Artemisia longifolia Long-leaved Sage Astragalus agrestis Purple Milk-vetch Astragalus flexuosus var. flexuosus Slender Milk-vetch Astragalus gilviflorus var gilviflorus Cushion Milk-vetch Astragalus laxmannii var. robustior Laxmann's Milk-vetch Astragalus lotiflorus Low Milk-vetch Astragalus missouriensis var missouriensis Missouri Milk-vetch Astragalus racemosus var. racemosus Racemose Milk-vetch Atriplex dioica Saline Saltbush Atriplex gardneri Nuttall's Atriplex Boechera grahamii Purple Rockcress Boechera retrofracta Reflexed Rockcress Bouteloua gracilis Blue Grama Bromus inermis* Smooth Brome Calamagrostis montanensis Plains Reed Grass Calamovilfa longifolia Prairie Sandreed Campanula rotundifolia Harebell Carex tenera Slender Sedge Chamaerhodos erecta Chamaerhodos Chamaesyce serpyllifolia ssp. serpyllifolia Thyme-leaf Sandmat Chenopodium album* Lamb's-quarters Chenopodium leptophyllum Narrow-leaved Goosefoot Cirsium flodmanii Flodman's Thistle Collomia linearis Narrow-leaved Collomia Comandra umbellata Pale Comandra Companula rotundifolia