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      Octosporaconidiophora (Pyronemataceae) – a new species from South Africa and the first report of anamorph in bryophilous Pezizales

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          Abstract

          Abstract

          Octospora conidiophora is described as a new species, based on collections from South Africa. It is characterised by apothecia with a distinct margin, smooth or finely warted ellipsoid ascospores, stiff, thick-walled hyaline hairs, warted mycelial hyphae and growth on pleurocarpous mosses Trichosteleum perchlorosum and Sematophyllum brachycarpum ( Hypnales ) on decaying wood in afromontane forests. It is the first species of bryophilous Pezizales in which an anamorph has been observed; it produces long, claviform, curved, hyaline and transversely septate conidia. Three other cryptic species of Octospora were detected using three molecular markers (LSU and SSU nrDNA and EF1α), but these could not be distinguished phenotypically. These are not described formally here and an informal species aggregate O. conidiophora agg. is established for them. The new species and finds of Lamprospora campylopodis growing on Campylopus pyriformis and Neottiella albocincta on Atrichum androgynum represent the first records of bryophilous Pezizales in South Africa.

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          The online database MaarjAM reveals global and ecosystemic distribution patterns in arbuscular mycorrhizal fungi (Glomeromycota).

          • Here, we describe a new database, MaarjAM, that summarizes publicly available Glomeromycota DNA sequence data and associated metadata. The goal of the database is to facilitate the description of distribution and richness patterns in this group of fungi. • Small subunit (SSU) rRNA gene sequences and available metadata were collated from all suitable taxonomic and ecological publications. These data have been made accessible in an open-access database (http://maarjam.botany.ut.ee). • Two hundred and eighty-two SSU rRNA gene virtual taxa (VT) were described based on a comprehensive phylogenetic analysis of all collated Glomeromycota sequences. Two-thirds of VT showed limited distribution ranges, occurring in single current or historic continents or climatic zones. Those VT that associated with a taxonomically wide range of host plants also tended to have a wide geographical distribution, and vice versa. No relationships were detected between VT richness and latitude, elevation or vascular plant richness. • The collated Glomeromycota molecular diversity data suggest limited distribution ranges in most Glomeromycota taxa and a positive relationship between the width of a taxon's geographical range and its host taxonomic range. Inconsistencies between molecular and traditional taxonomy of Glomeromycota, and shortage of data from major continents and ecosystems, are highlighted.
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            A rapid DNA isolation procedure for small quantities of fresh leaf tissue

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              Estimating the Phanerozoic history of the Ascomycota lineages: combining fossil and molecular data.

              The phylum Ascomycota is by far the largest group in the fungal kingdom. Ecologically important mutualistic associations such as mycorrhizae and lichens have evolved in this group, which are regarded as key innovations that supported the evolution of land plants. Only a few attempts have been made to date the origin of Ascomycota lineages by using molecular clock methods, which is primarily due to the lack of satisfactory fossil calibration data. For this reason we have evaluated all of the oldest available ascomycete fossils from amber (Albian to Miocene) and chert (Devonian and Maastrichtian). The fossils represent five major ascomycete classes (Coniocybomycetes, Dothideomycetes, Eurotiomycetes, Laboulbeniomycetes, and Lecanoromycetes). We have assembled a multi-gene data set (18SrDNA, 28SrDNA, RPB1 and RPB2) from a total of 145 taxa representing most groups of the Ascomycota and utilized fossil calibration points solely from within the ascomycetes to estimate divergence times of Ascomycota lineages with a Bayesian approach. Our results suggest an initial diversification of the Pezizomycotina in the Ordovician, followed by repeated splits of lineages throughout the Phanerozoic, and indicate that this continuous diversification was unaffected by mass extinctions. We suggest that the ecological diversity within each lineage ensured that at least some taxa of each group were able to survive global crises and rapidly recovered. Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Journal
                MycoKeys
                MycoKeys
                11
                urn:lsid:arphahub.com:pub:c004a564-9d6a-5f9f-b058-6a3815dfe9c3
                MycoKeys
                Pensoft Publishers
                1314-4057
                1314-4049
                2019
                10 June 2019
                : 54
                : 49-76
                Affiliations
                [1 ] Department of Botany, Faculty of Science, Palacký University Olomouc, Šlechtitelů 27, Olomouc, CZ-78371, Czech Republic Crop Research Institute, Centre of the Region Haná for Biotechnological and Agricultural Research Olomouc Czech Republic
                [2 ] Ludwig-Maximilians-Universität München, Systematische Botanik und Mykologie, Menzinger Straße 67, München, D-80638, Germany Palacký University Olomouc Olomouc Czech Republic
                [3 ] Department of Genetic Resources for Vegetables, Medicinal and Special Plants, Crop Research Institute, Centre of the Region Haná for Biotechnological and Agricultural Research, Šlechtitelů 29, Olomouc, CZ-78371, Czech Republic Universität München München Germany
                [4 ] National Herbarium, South African National Biodiversity Institute (SANBI), Private Bag X101, Pretoria 0001, South Africa National Herbarium, South African National Biodiversity Institute Pretoria South Africa
                [5 ] School of Animal, Plant and Environmental Sciences, University of the Witwatersrand, Johannesburg, PO WITS 2050, South Africa University of the Witwa­tersrand Johannesburg South Africa
                Author notes
                Corresponding author: Zuzana Sochorová ( asco.sochorova@ 123456gmail.com )

                Academic editor: D. Haelewaters

                Author information
                https://orcid.org/0000-0003-0022-9780
                Article
                34571
                10.3897/mycokeys.54.34571
                6579791
                72d993c0-2350-49e4-b417-2fa96113fdac
                Zuzana Sochorová, Peter Döbbeler, Michal Sochor, Jacques van Rooy

                This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 15 March 2019
                : 26 April 2019
                Funding
                Palacký University Ministry of Agriculture of the Czech Republic
                Categories
                Research Article
                Ascomycota
                Pyronemataceae
                Molecular Biology
                Phylogeny
                Taxonomy
                Africa

                afromontane forests,bryosymbionts,conidia,cryptic biodiversity,muscicolous parasites, sematophyllum , trichosteleum ,south africa,fungi,pezizales,pyronemataceae

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