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Dipterists Digest
Dipterists Digest 2019 Vol. 26 No. 1 Cover illustration: Eliozeta pellucens (Fallén, 1820), male (Tachinidae) . PORTUGAL: Póvoa Dão, Silgueiros, Viseu, N 40º 32' 59.81" / W 7º 56' 39.00", 10 June 2011, leg. Jorge Almeida (photo by Chris Raper). The first British record of this species is reported in the article by Ivan Perry (pp. 61-62). Dipterists Digest Vol. 26 No. 1 Second Series 2019 th Published 28 June 2019 Published by ISSN 0953-7260 Dipterists Digest Editor Peter J. Chandler, 606B Berryfield Lane, Melksham, Wilts SN12 6EL (E-mail: [email protected]) Editorial Panel Graham Rotheray Keith Snow Alan Stubbs Derek Whiteley Phil Withers Dipterists Digest is the journal of the Dipterists Forum . It is intended for amateur, semi- professional and professional field dipterists with interests in British and European flies. All notes and papers submitted to Dipterists Digest are refereed. Articles and notes for publication should be sent to the Editor at the above address, and should be submitted with a current postal and/or e-mail address, which the author agrees will be published with their paper. Articles must not have been accepted for publication elsewhere and should be written in clear and concise English. Contributions should be supplied either as E-mail attachments or on CD in Word or compatible formats. The scope of Dipterists Digest is: - the behaviour, ecology and natural history of flies; - new and improved techniques (e.g. collecting, rearing etc.); - the conservation of flies; - reports from the Diptera Recording Schemes, including maps; - records and assessments of rare or scarce species and those new to regions, countries etc.; - local faunal accounts and field meeting results, especially if accompanied by ecological or natural history interpretation; - descriptions of species new to science; - notes on identification and deletions or amendments to standard key works and checklists. -
Characterization of Two Undescribed Mucoralean Species with Specific
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 26 March 2018 doi:10.20944/preprints201803.0204.v1 1 Article 2 Characterization of Two Undescribed Mucoralean 3 Species with Specific Habitats in Korea 4 Seo Hee Lee, Thuong T. T. Nguyen and Hyang Burm Lee* 5 Division of Food Technology, Biotechnology and Agrochemistry, College of Agriculture and Life Sciences, 6 Chonnam National University, Gwangju 61186, Korea; [email protected] (S.H.L.); 7 [email protected] (T.T.T.N.) 8 * Correspondence: [email protected]; Tel.: +82-(0)62-530-2136 9 10 Abstract: The order Mucorales, the largest in number of species within the Mucoromycotina, 11 comprises typically fast-growing saprotrophic fungi. During a study of the fungal diversity of 12 undiscovered taxa in Korea, two mucoralean strains, CNUFC-GWD3-9 and CNUFC-EGF1-4, were 13 isolated from specific habitats including freshwater and fecal samples, respectively, in Korea. The 14 strains were analyzed both for morphology and phylogeny based on the internal transcribed 15 spacer (ITS) and large subunit (LSU) of 28S ribosomal DNA regions. On the basis of their 16 morphological characteristics and sequence analyses, isolates CNUFC-GWD3-9 and CNUFC- 17 EGF1-4 were confirmed to be Gilbertella persicaria and Pilobolus crystallinus, respectively.To the 18 best of our knowledge, there are no published literature records of these two genera in Korea. 19 Keywords: Gilbertella persicaria; Pilobolus crystallinus; mucoralean fungi; phylogeny; morphology; 20 undiscovered taxa 21 22 1. Introduction 23 Previously, taxa of the former phylum Zygomycota were distributed among the phylum 24 Glomeromycota and four subphyla incertae sedis, including Mucoromycotina, Kickxellomycotina, 25 Zoopagomycotina, and Entomophthoromycotina [1]. -
Records and Descriptions of North American Crane-Flies (Diptera)
Records and Descriptions of North American Crane-Flies (Diptera). Part III. Tipuloidea of the Upper Gunnison Valley, Colorado Charles P. Alexander American Midland Naturalist, Vol. 29, No. 1. (Jan., 1943), pp. 147-179. Stable URL: http://links.jstor.org/sici?sici=0003-0031%28194301%2929%3A1%3C147%3ARADONA%3E2.0.CO%3B2-V American Midland Naturalist is currently published by The University of Notre Dame. Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/about/terms.html. JSTOR's Terms and Conditions of Use provides, in part, that unless you have obtained prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, non-commercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at http://www.jstor.org/journals/notredame.html. Each copy of any part of a JSTOR transmission must contain the same copyright notice that appears on the screen or printed page of such transmission. The JSTOR Archive is a trusted digital repository providing for long-term preservation and access to leading academic journals and scholarly literature from around the world. The Archive is supported by libraries, scholarly societies, publishers, and foundations. It is an initiative of JSTOR, a not-for-profit organization with a mission to help the scholarly community take advantage of advances in technology. For more information regarding JSTOR, please contact [email protected]. -
Diversification of Fungal Chitinases and Their Functional Differentiation in 2 Histoplasma Capsulatum 3
bioRxiv preprint doi: https://doi.org/10.1101/2020.06.09.137125; this version posted June 16, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-ND 4.0 International license. 1 Diversification of fungal chitinases and their functional differentiation in 2 Histoplasma capsulatum 3 4 Kristie D. Goughenour1*, Janice Whalin1, 5 Jason C. Slot2, Chad A. Rappleye1# 6 7 1 Department of Microbiology, Ohio State University 8 2 Department of Plant Pathology, Ohio State University 9 10 11 #corresponding author: 12 [email protected] 13 614-247-2718 14 15 *current affiliation: 16 Division of Pulmonary and Critical Care Medicine 17 University of Michigan 18 VA Ann Arbor Healthcare System, Research Service 19 Ann Arbor, Michigan, USA 20 21 22 running title: Fungal chitinases 23 24 keywords: chitinase, GH18, fungi, Histoplasma 25 bioRxiv preprint doi: https://doi.org/10.1101/2020.06.09.137125; this version posted June 16, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-ND 4.0 International license. 26 ABSTRACT 27 Chitinases enzymatically hydrolyze chitin, a highly abundant biomolecule with many potential 28 industrial and medical uses in addition to their natural biological roles. Fungi are a rich source of 29 chitinases, however the phylogenetic and functional diversity of fungal chitinases are not well 30 understood. -
Fungal Evolution: Major Ecological Adaptations and Evolutionary Transitions
Biol. Rev. (2019), pp. 000–000. 1 doi: 10.1111/brv.12510 Fungal evolution: major ecological adaptations and evolutionary transitions Miguel A. Naranjo-Ortiz1 and Toni Gabaldon´ 1,2,3∗ 1Department of Genomics and Bioinformatics, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, Barcelona 08003, Spain 2 Department of Experimental and Health Sciences, Universitat Pompeu Fabra (UPF), 08003 Barcelona, Spain 3ICREA, Pg. Lluís Companys 23, 08010 Barcelona, Spain ABSTRACT Fungi are a highly diverse group of heterotrophic eukaryotes characterized by the absence of phagotrophy and the presence of a chitinous cell wall. While unicellular fungi are far from rare, part of the evolutionary success of the group resides in their ability to grow indefinitely as a cylindrical multinucleated cell (hypha). Armed with these morphological traits and with an extremely high metabolical diversity, fungi have conquered numerous ecological niches and have shaped a whole world of interactions with other living organisms. Herein we survey the main evolutionary and ecological processes that have guided fungal diversity. We will first review the ecology and evolution of the zoosporic lineages and the process of terrestrialization, as one of the major evolutionary transitions in this kingdom. Several plausible scenarios have been proposed for fungal terrestralization and we here propose a new scenario, which considers icy environments as a transitory niche between water and emerged land. We then focus on exploring the main ecological relationships of Fungi with other organisms (other fungi, protozoans, animals and plants), as well as the origin of adaptations to certain specialized ecological niches within the group (lichens, black fungi and yeasts). -
Bodenmikrobiologie (Version: 07/2019)
Langzeitmonitoring von Ökosystemprozessen - Methoden-Handbuch Modul 04: Bodenmikrobiologie (Version: 07/2019) www.hohetauern.at Impressum Impressum Für den Inhalt verantwortlich: Dr. Fernando Fernández Mendoza & Prof. Mag Dr. Martin Grube Institut für Biologie, Bereich Pflanzenwissenschaften, Universität Graz, Holteigasse 6, 8010 Graz Nationalparkrat Hohe Tauern, Kirchplatz 2, 9971 Matrei i.O. Titelbild: Ein Transekt im Untersuchungsgebiet Innergschlöss (2350 m üNN) wird im Jahr 2017 beprobt. © Newesely Zitiervorschlag: Fernández Mendoza F, Grube M (2019) Langzeitmonitoring von Ökosystemprozessen im Nationalpark Hohe Tauern. Modul 04: Mikrobiologie. Methoden-Handbuch. Verlag der Österreichischen Akademie der Wissenschaften, Wien. ISBN-Online: 978-3-7001-8752-3, doi: 10.1553/GCP_LZM_NPHT_Modul04 Weblink: https://verlag.oeaw.ac.at und http://www.parcs.at/npht/mmd_fullentry.php?docu_id=38612 Inhaltsverzeichnis Zielsetzung ...................................................................................................................................................... 1 Inhalt Vorbereitungsarbeit und benötigtes Material ................................................................................................... 2 a. Materialien für die Probenahme und Probenaufbewahrung ................................................................ 2 b. Materialien und Geräte für die Laboranalyse ...................................................................................... 2 Arbeitsablauf ................................................................................................................................................... -
Bringing a Trait‐Based Approach to Plant‐Associated Fungi
Biol. Rev. (2020), 95, pp. 409–433. 409 doi: 10.1111/brv.12570 Fungal functional ecology: bringing a trait-based approach to plant-associated fungi Amy E. Zanne1,∗ , Kessy Abarenkov2, Michelle E. Afkhami3, Carlos A. Aguilar-Trigueros4, Scott Bates5, Jennifer M. Bhatnagar6, Posy E. Busby7, Natalie Christian8,9, William K. Cornwell10, Thomas W. Crowther11, Habacuc Flores-Moreno12, Dimitrios Floudas13, Romina Gazis14, David Hibbett15, Peter Kennedy16, Daniel L. Lindner17, Daniel S. Maynard11, Amy M. Milo1, Rolf Henrik Nilsson18, Jeff Powell19, Mark Schildhauer20, Jonathan Schilling16 and Kathleen K. Treseder21 1Department of Biological Sciences, George Washington University, Washington, DC 20052, U.S.A. 2Natural History Museum, University of Tartu, Vanemuise 46, Tartu 51014, Estonia 3Department of Biology, University of Miami, Coral Gables, FL 33146, U.S.A. 4Freie Universit¨at-Berlin, Berlin-Brandenburg Institute of Advanced Biodiversity Research, 14195 Berlin, Germany 5Department of Biological Sciences, Purdue University Northwest, Westville, IN 46391, U.S.A. 6Department of Biology, Boston University, Boston, MA 02215, U.S.A. 7Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR 97330, U.S.A. 8Department of Plant Biology, University of Illinois Urbana-Champaign, Urbana, IL 61801, U.S.A. 9Department of Biology, University of Louisville, Louisville, KY 40208, U.S.A. 10Evolution & Ecology Research Centre, School of Biological Earth and Environmental Sciences, University of New South Wales, Sydney, New South Wales 2052, Australia 11Department of Environmental Systems Science, Institute of Integrative Biology, ETH Z¨urich, 8092, Z¨urich, Switzerland 12Department of Ecology, Evolution, and Behavior, and Department of Forest Resources, University of Minnesota, St. Paul, MN 55108, U.S.A. -
Subphyl. Nov., Based on Multi-Gene Genealogies
ISSN (print) 0093-4666 © 2011. Mycotaxon, Ltd. ISSN (online) 2154-8889 MYCOTAXON Volume 115, pp. 353–363 January–March 2011 doi: 10.5248/115.353 Mortierellomycotina subphyl. nov., based on multi-gene genealogies K. Hoffmann1*, K. Voigt1 & P.M. Kirk2 1 Jena Microbial Resource Collection, Institute of Microbiology, University of Jena, Neugasse 25, 07743 Jena, Germany 2 CABI UK Centre, Bakeham Lane, Egham, Surrey TW20 9TY, United Kingdom *Correspondence to: Hoff[email protected] Abstract — TheMucoromycotina unifies two heterogenous orders of the sporangiferous, soil- inhabiting fungi. The Mucorales comprise saprobic, occasionally facultatively mycoparasitic, taxa bearing a columella, whereas the Mortierellales encompass mainly saprobic fungi lacking a columella. Multi-locus phylogenetic analyses based on eight nuclear genes encoding 18S and 28S rRNA, actin, alpha and beta tubulin, translation elongation factor 1alpha, and RNA polymerase II subunits 1 and 2 provide strong support for separation of the Mortierellales from the Mucoromycotina. The existence of a columella is shown to serve as a synapomorphic morphological trait unique to Mucorales, supporting the taxonomic separation of the acolumellate Mortierellales from the columellate Mucoromycotina. Furthermore, irregular hyphal septation and development of subbasally vesiculate sporangiophores bearing single terminal sporangia strongly correlate with the phylogenetic delimitation of Mortierellales, supporting a new subphylum, Mortierellomycotina. Key words — Zygomycetes, SSU rDNA, LSU rDNA, protein-coding genes, monophyly Introduction The type species ofMortierella Coem. 1863, M. polycephala Coem. 1863, was originally isolated from a parasitic interaction with a mushroom and named in honour of M. Du Mortier, the president of the Société de Botanique de Belgique (Coemans 1863). However, the common habit of mortierellalean species is as soil saprobes, enabling the fungi to grow on excrements, decaying plants, or (not infrequently) on decaying mushrooms and mucoralean fungi (Fischer 1892). -
Examining New Phylogenetic Markers to Uncover The
Persoonia 30, 2013: 106–125 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158513X666394 Examining new phylogenetic markers to uncover the evolutionary history of early-diverging fungi: comparing MCM7, TSR1 and rRNA genes for single- and multi-gene analyses of the Kickxellomycotina E.D. Tretter1, E.M. Johnson1, Y. Wang1, P. Kandel1, M.M. White1 Key words Abstract The recently recognised protein-coding genes MCM7 and TSR1 have shown significant promise for phylo genetic resolution within the Ascomycota and Basidiomycota, but have remained unexamined within other DNA replication licensing factor fungal groups (except for Mucorales). We designed and tested primers to amplify these genes across early-diverging Harpellales fungal clades, with emphasis on the Kickxellomycotina, zygomycetous fungi with characteristic flared septal walls Kickxellomycotina forming pores with lenticular plugs. Phylogenetic tree resolution and congruence with MCM7 and TSR1 were com- MCM7 pared against those inferred with nuclear small (SSU) and large subunit (LSU) rRNA genes. We also combined MS277 MCM7 and TSR1 data with the rDNA data to create 3- and 4-gene trees of the Kickxellomycotina that help to resolve MS456 evolutionary relationships among and within the core clades of this subphylum. Phylogenetic inference suggests ribosomal biogenesis protein that Barbatospora, Orphella, Ramicandelaber and Spiromyces may represent unique lineages. It is suggested that Trichomycetes these markers may be more broadly useful for phylogenetic studies among other groups of early-diverging fungi. TSR1 Zygomycota Article info Received: 27 June 2012; Accepted: 2 January 2013; Published: 20 March 2013. INTRODUCTION of Blastocladiomycota and Kickxellomycotina, as well as four species of Mucoromycotina have their genomes available The molecular revolution has transformed our understanding of (based on available online searches and the list at http://www. -
Trichomycetes from Lentic and Lotic Aquatic Habitats in Ontario, Canada
1449 Trichomycetes from lentic and lotic aquatic habitats in Ontario, Canada D.B. Strongman and Merlin M. White Abstract: Fungi and protists make up an ecological group, trichomycetes, that inhabit the guts of invertebrates, mostly aquatic insects. Trichomycetes are reported herein from arthropods collected in lotic habitats (fast flowing streams) and lentic environments (ponds, ditches, seeps, and lakes) from 11 sites in Algonquin Park and 6 other sites in Ontario, Can- ada. Thirty-two trichomycete species were recovered, including 7 new species: Legeriomyces algonquinensis, Legeriosi- milis leptocerci, Legeriosimilis whitneyi, and Paramoebidium umbonatum are described from mayfly nymphs (Ephemeroptera); Pennella digitata and Glotzia incilis from black fly and midge larvae (Diptera), respectively; and Arun- dinula opeongoensis from a crayfish (Crustacea). Legeriomyces rarus Lichtw. & M.C. Williams and Stachylina penetralis Lichtw. are new North American records, and seven species are documented for the first time in Canada. More common and widely distributed trichomycete species such as Harpella melusinae Le´ger & Duboscq and Smittium culicis Manier, were also recovered. Most previous studies on trichomycetes have been done primarily in lotic environments but clearly lentic systems (e.g., ponds and lakes) harbour diverse arthropod communities and further exploration of these habitats will continue to increase our knowledge of trichomycete diversity. Key words: Amoebidiales, Eccrinales, Harpellales, insect fungal endobionts, symbiotic protista. Re´sume´ : Les champignons et les protistes comportent un groupe e´cologique, les trichomyce`tes, qui habitent les intestins de la plupart des insectes aquatiques. Les auteurs rapportent des ttrichomyce`tes provenant d’arthropodes vivants dans des habitats lotiques (cours d’eau rapides) et des environnements lentiques (e´tangs, fosse´s, suintement et lacs) re´colte´s sur 11 sites dans le parc Algonquin et six autres sites en Ontario, au Canada. -
Dipterists Digest
Dipterists Digest 2018 Vol. 25 No. 2 Cover illustration: Palloptera usta (Meigen, 1826) (Pallopteridae), male, on a rotten birch log at Glen Affric (NH 28012832), 4 November 2018. © Alan Watson Featherstone. In Britain, a predominantly Scottish species, having strong associations with Caledonian pine forest, but also developing in wood of broad-leaved trees. Rearing records from under bark of Betula (3), Fraxinus (1), Picea (18), Pinus (21), Populus (2) and Quercus (1) were cited by G.E. Rotheray and R.M. Lyszkowski (2012. Pallopteridae (Diptera) in Scotland. Dipterists Digest (Second Series ) 19, 189- 203). Apparently a late date, as the date range given by Rotheray and Lyszkowski ( op. cit .) for both adult captures and emergence dates from puparia was 13 May to 29 September. Dipterists Digest Vol. 25 No. 2 Second Series 2018 th Published 27 February 2019 Published by ISSN 0953-7260 Dipterists Digest Editor Peter J. Chandler, 606B Berryfield Lane, Melksham, Wilts SN12 6EL (E-mail: [email protected]) Editorial Panel Graham Rotheray Keith Snow Alan Stubbs Derek Whiteley Phil Withers Dipterists Digest is the journal of the Dipterists Forum . It is intended for amateur, semi- professional and professional field dipterists with interests in British and European flies. All notes and papers submitted to Dipterists Digest are refereed. Articles and notes for publication should be sent to the Editor at the above address, and should be submitted with a current postal and/or e-mail address, which the author agrees will be published with their paper. Articles must not have been accepted for publication elsewhere and should be written in clear and concise English. -
Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes
University of Rhode Island DigitalCommons@URI Biological Sciences Faculty Publications Biological Sciences 9-26-2018 Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes Christopher E. Lane Et Al Follow this and additional works at: https://digitalcommons.uri.edu/bio_facpubs Journal of Eukaryotic Microbiology ISSN 1066-5234 ORIGINAL ARTICLE Revisions to the Classification, Nomenclature, and Diversity of Eukaryotes Sina M. Adla,* , David Bassb,c , Christopher E. Laned, Julius Lukese,f , Conrad L. Schochg, Alexey Smirnovh, Sabine Agathai, Cedric Berneyj , Matthew W. Brownk,l, Fabien Burkim,PacoCardenas n , Ivan Cepi cka o, Lyudmila Chistyakovap, Javier del Campoq, Micah Dunthornr,s , Bente Edvardsent , Yana Eglitu, Laure Guillouv, Vladimır Hamplw, Aaron A. Heissx, Mona Hoppenrathy, Timothy Y. Jamesz, Anna Karn- kowskaaa, Sergey Karpovh,ab, Eunsoo Kimx, Martin Koliskoe, Alexander Kudryavtsevh,ab, Daniel J.G. Lahrac, Enrique Laraad,ae , Line Le Gallaf , Denis H. Lynnag,ah , David G. Mannai,aj, Ramon Massanaq, Edward A.D. Mitchellad,ak , Christine Morrowal, Jong Soo Parkam , Jan W. Pawlowskian, Martha J. Powellao, Daniel J. Richterap, Sonja Rueckertaq, Lora Shadwickar, Satoshi Shimanoas, Frederick W. Spiegelar, Guifre Torruellaat , Noha Youssefau, Vasily Zlatogurskyh,av & Qianqian Zhangaw a Department of Soil Sciences, College of Agriculture and Bioresources, University of Saskatchewan, Saskatoon, S7N 5A8, SK, Canada b Department of Life Sciences, The Natural History Museum, Cromwell Road, London, SW7 5BD, United Kingdom